<\/p>\n
Structural formula<\/p>\n
Aliphatic halogenated derivatives<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
CAS number:<\/b>96-18-4<\/p>\n
MDL number:<\/b>MFCD00000946<\/p>\n
EINECS number:<\/b>202-486-1<\/p>\n
RTECS number:<\/b>TZ9275000<\/p>\n
BRN number:<\/b>1732068<\/p>\n
PubChem number:<\/b>24869995<\/p>\nPhysical property data<\/h2>\n
1. Properties: colorless to light yellow liquid with chloroform smell. [1]<\/sup><\/p>\n2. Melting point (\u2103): -14.7[2]<\/sup><\/p>\n3. Boiling point (\u2103): 156.8[3]<\/sup><\/p>\n4. Relative density (water=1): 1.39 (20\u2103)[4]<\/sup><\/p>\n 5. Relative vapor density (air = 1): 5.0[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 1.33 (46\u2103)[6]<\/sup><\/p>\n7. Heat of combustion (kJ\/mol): -1733.0[7]<\/sup><\/p>\n8. Critical pressure (MPa): 3.87[8]<\/sup><\/p>\n9. Octanol\/water partition coefficient: 2.27[9]<\/sup><\/p>\n10. Flash point (\u2103): 71.1 (CC); 82.2 (OC) [10]<\/sup><\/p>\n11. Ignition temperature (\u2103): 304[11]<\/sup><\/p>\n12. Explosion upper limit (%): 12.6[12]<\/sup><\/p>\n13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Melting point (\u2103): -14.7[2]<\/sup><\/p>\n3. Boiling point (\u2103): 156.8[3]<\/sup><\/p>\n4. Relative density (water=1): 1.39 (20\u2103)[4]<\/sup><\/p>\n 5. Relative vapor density (air = 1): 5.0[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 1.33 (46\u2103)[6]<\/sup><\/p>\n7. Heat of combustion (kJ\/mol): -1733.0[7]<\/sup><\/p>\n8. Critical pressure (MPa): 3.87[8]<\/sup><\/p>\n9. Octanol\/water partition coefficient: 2.27[9]<\/sup><\/p>\n10. Flash point (\u2103): 71.1 (CC); 82.2 (OC) [10]<\/sup><\/p>\n11. Ignition temperature (\u2103): 304[11]<\/sup><\/p>\n12. Explosion upper limit (%): 12.6[12]<\/sup><\/p>\n13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Boiling point (\u2103): 156.8[3]<\/sup><\/p>\n4. Relative density (water=1): 1.39 (20\u2103)[4]<\/sup><\/p>\n 5. Relative vapor density (air = 1): 5.0[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 1.33 (46\u2103)[6]<\/sup><\/p>\n7. Heat of combustion (kJ\/mol): -1733.0[7]<\/sup><\/p>\n8. Critical pressure (MPa): 3.87[8]<\/sup><\/p>\n9. Octanol\/water partition coefficient: 2.27[9]<\/sup><\/p>\n10. Flash point (\u2103): 71.1 (CC); 82.2 (OC) [10]<\/sup><\/p>\n11. Ignition temperature (\u2103): 304[11]<\/sup><\/p>\n12. Explosion upper limit (%): 12.6[12]<\/sup><\/p>\n13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Relative density (water=1): 1.39 (20\u2103)[4]<\/sup><\/p>\n 5. Relative vapor density (air = 1): 5.0[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 1.33 (46\u2103)[6]<\/sup><\/p>\n7. Heat of combustion (kJ\/mol): -1733.0[7]<\/sup><\/p>\n8. Critical pressure (MPa): 3.87[8]<\/sup><\/p>\n9. Octanol\/water partition coefficient: 2.27[9]<\/sup><\/p>\n10. Flash point (\u2103): 71.1 (CC); 82.2 (OC) [10]<\/sup><\/p>\n11. Ignition temperature (\u2103): 304[11]<\/sup><\/p>\n12. Explosion upper limit (%): 12.6[12]<\/sup><\/p>\n13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
5. Relative vapor density (air = 1): 5.0[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 1.33 (46\u2103)[6]<\/sup><\/p>\n7. Heat of combustion (kJ\/mol): -1733.0[7]<\/sup><\/p>\n8. Critical pressure (MPa): 3.87[8]<\/sup><\/p>\n9. Octanol\/water partition coefficient: 2.27[9]<\/sup><\/p>\n10. Flash point (\u2103): 71.1 (CC); 82.2 (OC) [10]<\/sup><\/p>\n11. Ignition temperature (\u2103): 304[11]<\/sup><\/p>\n12. Explosion upper limit (%): 12.6[12]<\/sup><\/p>\n13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
6. Saturated vapor pressure (kPa): 1.33 (46\u2103)[6]<\/sup><\/p>\n7. Heat of combustion (kJ\/mol): -1733.0[7]<\/sup><\/p>\n8. Critical pressure (MPa): 3.87[8]<\/sup><\/p>\n9. Octanol\/water partition coefficient: 2.27[9]<\/sup><\/p>\n10. Flash point (\u2103): 71.1 (CC); 82.2 (OC) [10]<\/sup><\/p>\n11. Ignition temperature (\u2103): 304[11]<\/sup><\/p>\n12. Explosion upper limit (%): 12.6[12]<\/sup><\/p>\n13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
7. Heat of combustion (kJ\/mol): -1733.0[7]<\/sup><\/p>\n8. Critical pressure (MPa): 3.87[8]<\/sup><\/p>\n9. Octanol\/water partition coefficient: 2.27[9]<\/sup><\/p>\n10. Flash point (\u2103): 71.1 (CC); 82.2 (OC) [10]<\/sup><\/p>\n11. Ignition temperature (\u2103): 304[11]<\/sup><\/p>\n12. Explosion upper limit (%): 12.6[12]<\/sup><\/p>\n13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
8. Critical pressure (MPa): 3.87[8]<\/sup><\/p>\n9. Octanol\/water partition coefficient: 2.27[9]<\/sup><\/p>\n10. Flash point (\u2103): 71.1 (CC); 82.2 (OC) [10]<\/sup><\/p>\n11. Ignition temperature (\u2103): 304[11]<\/sup><\/p>\n12. Explosion upper limit (%): 12.6[12]<\/sup><\/p>\n13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
9. Octanol\/water partition coefficient: 2.27[9]<\/sup><\/p>\n10. Flash point (\u2103): 71.1 (CC); 82.2 (OC) [10]<\/sup><\/p>\n11. Ignition temperature (\u2103): 304[11]<\/sup><\/p>\n12. Explosion upper limit (%): 12.6[12]<\/sup><\/p>\n13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
10. Flash point (\u2103): 71.1 (CC); 82.2 (OC) [10]<\/sup><\/p>\n11. Ignition temperature (\u2103): 304[11]<\/sup><\/p>\n12. Explosion upper limit (%): 12.6[12]<\/sup><\/p>\n13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
11. Ignition temperature (\u2103): 304[11]<\/sup><\/p>\n12. Explosion upper limit (%): 12.6[12]<\/sup><\/p>\n13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
12. Explosion upper limit (%): 12.6[12]<\/sup><\/p>\n13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
13. Explosion lower limit (%): 3.2[13]<\/sup><\/p>\n14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
14. Solubility: Slightly soluble in water, soluble in ethanol, ether, oils, lipids, and paraffin. [14]<\/sup><\/p>\n15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n16. Flash point (\u00baC, closed): 73.3<\/p>\n17. Flash point (\u00baC, open): 78.9<\/p>\n18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n 22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
15. Viscosity (mPa\u00b7s, 20\u00baC): 0.2505<\/p>\n
16. Flash point (\u00baC, closed): 73.3<\/p>\n
17. Flash point (\u00baC, open): 78.9<\/p>\n
18. Vapor pressure (kPa, 9.0\u00baC): 0.13<\/p>\n
19. Vapor pressure (kPa, 46.0\u00baC ): 1.33<\/p>\n
20. Heat of evaporation (KJ\/mol, b.p.): 40.56<\/p>\n
21. Heat of combustion (KJ\/mol, liquid): 1735.9<\/p>\n
22. Specific heat capacity (KJ\/(kg\u00b7K), 20\u00baC): 1.235<\/p>\n
23. Volume expansion coefficient (K-1<\/sup>, 20\u00baC): 0.00096<\/p>\n24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
24. Relative density (25\u2103, 4\u2103): 1.3832<\/p>\n
25. Refractive index at room temperature (n25<\/sup>): 1.4812<\/p>\n26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
26. Solubility Parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 20.148<\/p>\n27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
27.van der Waals area (cm2<\/sup>\u00b7mol -1<\/sup>): 8.690\u00d7109<\/sup><\/p>\n28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
28. van der Waals volume (cm3<\/sup>\u00b7mol -1<\/sup>): 62.720<\/p>\n29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
29. Gas phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -182.9<\/p>\n30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
30 .Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -230.6<\/p>\n31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
31. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 172.4<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Acute toxicity[15]<\/sup> <\/strong><\/p>\nLD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\nLC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
LD50: 108\u03bcl (150mg)\/kg (rat oral); 369mg\/kg ( Mouse oral); 372\u03bcl (517mg)\/kg (rabbit transdermal)<\/p>\n
LC50: 3400mg\/m3<\/sup> (mouse inhalation, 2h)<\/p>\n2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Irritation[16]<\/sup><\/strong><\/p>\nRabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\nRabbit eye: 100\u03bcl, moderate irritation. <\/p>\n3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Rabbit transdermal: 500\u03bcl (24h), mild irritation. <\/p>\n
Rabbit eye: 100\u03bcl, moderate irritation. <\/p>\n
3. Mutagenicity [17]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 500ng\/dish. DNA damage: human lymphocytes 2mmol\/L. Cytogenetic analysis: Rats inhaled 800\u03bcg\/L. Sister chromatid exchange: hamster lung 300 \u03bcmol\/L. <\/p>\n4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Carcinogenicity[18]<\/sup><\/strong> IARC Carcinogenicity\ufffd\ufffdComment: G2A, possible human carcinogen. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Ecotoxicity[19]<\/sup><\/strong><\/p>\nLC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\nEC50: 45mg\/L (24h) (Daphnia)<\/p>\n2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
LC50: 42mg\/L (7d) (Rainbow killifish); 109mg\/L (48h) (Medaka)<\/p>\n
EC50: 45mg\/L (24h) (Daphnia)<\/p>\n
2. Biodegradability [20]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 4320~8640<\/p>\nAnaerobic biodegradation (h): 17280~34560<\/p>\n3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Aerobic biodegradation (h): 4320~8640<\/p>\n
Anaerobic biodegradation (h): 17280~34560<\/p>\n
3. Non-biodegradability[21]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 61~613<\/p>\nFirst-order hydrolysis half-life (h ): 44<\/p>\n4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Photooxidation half-life in air (h): 61~613<\/p>\n
First-order hydrolysis half-life (h ): 44<\/p>\n
4. Other harmful effects [22]<\/sup><\/strong> This substance is harmful to the environment and has an accumulation effect in groundwater. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 30.45<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Molar refractive index: 30.45<\/p>\n
2. Molar volume (cm3<\/sup>\/mol): 112.5<\/p>\n3. Isotonic specific volume (90.2K ): 264.2<\/p>\n4. Surface tension (dyne\/cm): 30.3<\/p>\n5. Polarizability: 12.07<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 2<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 25.2<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Isotonic specific volume (90.2K ): 264.2<\/p>\n
4. Surface tension (dyne\/cm): 30.3<\/p>\n
5. Polarizability: 12.07<\/p>\n<\/p>\n
1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n
2. Number of hydrogen bond donors: 0<\/p>\n
3. Number of hydrogen bond acceptors: 0<\/p>\n
4. Number of rotatable chemical bonds: 2<\/p>\n
5. Number of tautomers: none<\/p>\n
6. Topological molecule polar surface area 0<\/p>\n
7. Number of heavy atoms: 6<\/p>\n
8. Surface charge: 0<\/p>\n
9. Complexity: 25.2<\/p>\n
10. Number of isotope atoms: 0<\/p>\n
11. Determine the number of atomic stereocenters: 0<\/p>\n
12. Uncertain number of atomic stereocenters: 0<\/p>\n
13. Determine the number of chemical bond stereocenters: 0 <\/p>\n
14. Number of uncertain chemical bond stereocenters: 0<\/p>\n
15. Number of covalent bond units: 1<\/p>\n<\/p>\n
1. It is slightly corrosive to metals. When water is present, it decomposes into highly corrosive hydrogen chloride. Light can accelerate this decomposition. The acidity of 1,2,3-trichloropropane that has been stored or recycled for a long time should be checked before use. Toxic gases are produced during pyrolysis or combustion, so contact with red-hot objects should be avoided. <\/p>\n
2. When heated with solid potassium hydroxide, hydrogen chloride is removed, and the main product of the reaction is 1,3-dichloropropene and a small amount of 2,3-dichloropropene. It is heated under pressure with water or sodium bicarbonate aqueous solution in the presence of copper to generate glycerin. <\/p>\n
3. Stability[23]<\/sup><\/strong> Stable<\/p>\n4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Incompatible substances[24] <\/sup><\/strong> Strong oxidizing agent, strong alkali<\/p>\n5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
5. Conditions to avoid contact[25]<\/sup><\/strong> Moist air, light, heat<\/p>\n6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
6. Polymerization hazard[26]<\/sup><\/strong> No polymerization<\/p>\n7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
7. Decomposition products[27]<\/sup><\/strong> Hydrogen chloride<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Storage Precautions[28]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n<\/p>\n2. Dichloroisopropanol Law. <\/p>\n<\/p>\n<\/p>\nPurpose<\/h2>\n1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. \u03b1-Propylene chloride chlorination method: Propylene is chlorinated at high temperature to obtain allyl chloride. After washing and separation, it is then chlorinated at low temperature and fractionated to obtain the finished product. <\/p>\n
2. Dichloroisopropanol Law. <\/p>\n
<\/p>\n<\/p>\n
1. Used to produce pesticides, organic synthesis, and gas chromatography comparison samples. Used as a paint stripper for varnishes and coatings, and a solvent for engine cleaning. It can also be used as a raw material for pesticides such as chlormequat and Oat Di No. 1. <\/p>\n
2. Used as solvent and intermediate. [29]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
extended-reading:https:\/\/www.bdmaee.net\/dibutyltin-monobutyl-maleate\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5394\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-stannous-octoate-soft-foam-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/2-dimethylamineethanol\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-ne500-dabco-strong-gel-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45071<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44112<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-mb20-bismuth-metal-carboxylate-catalyst-catalyst-dabco-mb20\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44245<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Structural formula Business number 02AM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48702,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[532,24,15277],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48703"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48703\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48702"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48703"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48703"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48703"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
![\"1,2,3-Trichloropropane](\"http:\/\/www.newtopchem.com\/wp-content\/uploads\/2024\/05\/5a3a00cdb42344a38be1091fa391eb68.gif\")
<\/p>\n<\/p>\n![\"\"](\"http:\/\/www.newtopchem.com\/wp-content\/uploads\/2024\/05\/201009011410431334.gif\")
<\/p>\n![\"\"](\"http:\/\/images.basechem.org\/internal\/day_100901\/201009011410555287.gif\")
<\/p>\n<\/p>\n![https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg<\/a><\/br>extended-reading:](\"https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/129.jpg\"){kind=link}