<\/p>\n
Structural formula<\/p>\n
2-(2,2-Diphenylacetyl)-1,3-indandione,<\/p>\n
Diphacin sodium,<\/p>\n
Dibenzofen,<\/p>\n
enemy rats,<\/p>\n
wild squirrel net,<\/p>\n
Didandin,<\/p>\n
Dipaxin,<\/p>\n
Diphenacin,<\/p>\n
Rodenticide<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
CAS number:<\/b>82-66-6<\/p>\n
MDL number:<\/b>None<\/p>\n
EINECS number:<\/b>201-434-5<\/p>\n
RTECS number:<\/b>NK5600000<\/p>\n
BRN number:<\/b>None<\/p>\n
PubChem ID:<\/b>None<\/p>\nPhysical property data<\/h2>\n
1. Properties: light yellow powder, the pure product is odorless and tasteless, the original drug has a slight smell<\/p>\n
2. Density (g\/mL, 25\/4\u2103): Uncertain<\/p>\n
3. Relative vapor density (g\/mL, air=1): Uncertain<\/p>\n
4. Melting point (\u00baC): 145~<\/span>147<\/p>\n5. Boiling point (\u00baC, normal pressure): Uncertain<\/p>\n6. Boiling point (\u00baC, 5.2kPa): Uncertain<\/p>\n7 . Refractive index: Uncertain<\/p>\n8. Flash point (\u00baC): Uncertain<\/p>\n9. Specific rotation (\u00ba): Uncertain<\/p>\n10. Autoignition point or ignition temperature (\u00baC): Uncertain<\/p>\n11. Vapor pressure (kPa, 25\u00baC): Uncertain<\/p>\n12. Saturated vapor pressure (kPa, 60\u00baC): Uncertain Determine<\/p>\n13. Heat of combustion (KJ\/mol): Uncertain<\/p>\n14. Critical temperature (\u00baC): Uncertain<\/p>\n15. Critical pressure (KPa ): Uncertain<\/p>\n16. Log value of oil-water (octanol\/water) partition coefficient: Uncertain<\/p>\n17. Explosion upper limit (%, V\/V): Uncertain<\/p>\n18. Lower explosion limit (%, V\/V): Uncertain<\/p>\n19. Solubility: soluble in alcohol and acetone, soluble in hot water, insoluble in benzene and toluene. <\/p>\n<\/p>\nToxicological data<\/h2>\nAcute toxicity:<\/p>\nRat caliber LD50: 1500 ug\/kg; rat inhalation LC50: 2 gm\/m3\/4H<\/p>\nRat skin LD50: 200mg\/kg; Rat LD50: 11mg\/kg;<\/p>\nMouse LD50: 28300 ug\/kg; Mouse LD50: 300mg\/kg<\/p>\nDog LD50: 3mg\/kg;<\/p>\nCat caliber LD50: 15mg\/kg;<\/p>\nRabbit caliber LD50: 35mg\/kg;\uff40<\/p>\nPig caliber LD50: 1\uff15mg\/kg;\uff40<\/p>\nDuck caliber LD50: 3158mg\/kg; <\/p>\n Breeding animal LD50: 910ug\/kg;\n <\/p>\nEcological MathematicsAccording to<\/h2>\n\n None yet\n <\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 96.78<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 267.3<\/p>\n3. Isotonic specific volume (90.2K ): 731.7<\/p>\n4. Surface tension (dyne\/cm): 56.1<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 38.56<\/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: 3<\/p>\n4. Number of rotatable chemical bonds: 4<\/p>\n5. Number of tautomers: 5<\/p>\n6. Topological molecule polar surface area 51.2<\/p>\n7. Number of heavy atoms: 26<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 512<\/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>\nThe sodium salt (often called diphacin sodium salt) has a solubility of 5% in water at 100\u00b0C. It changes from yellow to red when heated to 207-208\u00b0C and decomposes at 325\u00b0C. <\/p>\n<\/p>\nStorage method<\/h2>\nStored sealed and protected from light. <\/p>\nDuring storage and transportation, it must be protected from moisture and sunlight, kept ventilated, and must not be mixed with food, seeds, or feed.\n <\/p>\nSynthesis method<\/h2>\n1. Preparation of phenylacetone. Industrially, phenylacetamide is used as raw material and reacted at 110-130\u00b0C for 2 hours in the presence of concentrated sulfuric acid to obtain phenylacetic acid. Phenylacetic acid and acetic anhydride react under the catalysis of anhydrous sodium acetate at 140-150\u00b0C for 18 hours. The acetic acid generated continues to steam out. After the reaction, add an appropriate amount of cold water and separate the water layer. The crude phenyl acetone is dissolved in 100% sodium hydroxide with 20% sodium hydroxide. Stir at ~110\u00b0C for 2 hours, and control the pH value to 12. 2. Preparation of diphenyl acetone. Add bromine dropwise into the phenyl acetone mixture, and control the temperature to less than 30\u00b0C to prevent incomplete bromination caused by excessive volatilization of bromine. After the reaction is completed, remove the residual Hydrogen bromide. Then, the generated bromide is added dropwise to the pure benzene liquid under negative pressure, and anhydrous aluminum trichloride is used as the catalyst. The reaction is carried out at room temperature for 3 to 4 hours, and then post-processed to obtain diphenylacetone. 3. Synthesis of diphacin and diphacin sodium salt. Put the solvent toluene and the catalyst sodium methoxide into the reaction pot, raise the temperature to 110\u00b0C, add dimethyl phthalate and toluene mixture after azeotropy, and add diphenyl diphenyl dropwise Add a toluene mixture of acetone and react at 100-120\u00b0C for 1.5-2 hours. In acidic or neutral media, the product obtained is diphacin, and in alkaline medium, diphacin sodium salt is obtained. Sodium methoxide is a strong base, and its amount determines the ratio of the two products (diphacin and diphacin sodium salt). <\/p>\n4.Phenyl acetone is generated from the acylation reaction of phenylacetic acid and acetic anhydride, and phenyl acetone is generated through bromination and phenylation reactions. Diphenyl acetone. Then, the solvent toluene and the catalyst sodium methoxide are put into the reactor, and after azeotropy, a mixture of dimethyl phthalate and toluene is added, and a toluene mixture of partial diphenylacetone is added dropwise. In acidic or neutral media, the product is dimethonium, and in alkaline medium, dimethin sodium salt is obtained. <\/span><\/p>\n<\/p>\nPurpose<\/h2>\n1. Chronic rodenticide. It is the first generation anticoagulant that is widely used. It has broad target spectrum, good palatability, slow action and obvious effect. When a lethal dose is taken, it destroys the hyperthrombin in the blood of rats, prolongs the coagulation time, and causes massive internal bleeding and hypoxia in the rat’s internal organs. Therefore, most rats will run out of the hole before death and become listless and sluggish until they die. Used to kill domestic rats in residences, grain depots, vehicle and ship docks and other places. It can also be used to kill wild rats in dry fields, rice fields, forest areas and grasslands. Use 0.25\u2030~0.5\u2030 poisoning for multiple times in a row. You can also use 1\u2030 poison bait once. Most poisonous baits are prepared with rice or noodles, but you can also use sweet potato shreds, carrot shreds and other baits. For other foods that rats like to eat, add 2% to 5% cooking oil for better results. For example, the preparation of 0.5\u2030 rice bait: Dissolve 0.5g of diphacin sodium salt in an appropriate amount of hot water (above 80\u00b0C), soak it in 1000g of rice to evenly absorb the agent, and dry it to make rice bait. Or dissolve 0.5g of diphacin sodium salt in an appropriate amount of hot water, mix it with 1000g of flour and bake it into dough cakes to make dough bait. <\/p>\n2.It is an anticoagulant rodenticide. It has broad target spectrum, good palatability, slow action and obvious effect. When a lethal dose is taken, it destroys the hyperthrombin in the blood of rats, prolongs the coagulation time, and causes massive internal bleeding and hypoxia in rats until death. Used to kill domestic rats in residences, grain depots, vehicle and ship docks and other places. It can also be used for rodent control in dry fields, rice fields, forest areas and grasslands. Most poisonous baits are prepared with rice or noodles, but sweet potato shreds, carrot shreds and other baits can also be used. <\/span><\/p>\n<\/p>\n extended-reading:https:\/\/www.newtopchem.com\/archives\/64<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat9201-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-c-124-low-odor-tertiary-amine-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2021\/05\/138-3.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/3164-85-0\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat4210-catalyst-cas-683-18-1-dibutyltin-dichloride\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/71.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/coordinated-thiol-methyltin\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40422<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44919<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01T2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48480,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15207],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481"}],"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=48481"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48480"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48481"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48481"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48481"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
5. Boiling point (\u00baC, normal pressure): Uncertain<\/p>\n
6. Boiling point (\u00baC, 5.2kPa): Uncertain<\/p>\n
7 . Refractive index: Uncertain<\/p>\n
8. Flash point (\u00baC): Uncertain<\/p>\n
9. Specific rotation (\u00ba): Uncertain<\/p>\n
10. Autoignition point or ignition temperature (\u00baC): Uncertain<\/p>\n
11. Vapor pressure (kPa, 25\u00baC): Uncertain<\/p>\n
12. Saturated vapor pressure (kPa, 60\u00baC): Uncertain Determine<\/p>\n
13. Heat of combustion (KJ\/mol): Uncertain<\/p>\n
14. Critical temperature (\u00baC): Uncertain<\/p>\n
15. Critical pressure (KPa ): Uncertain<\/p>\n
16. Log value of oil-water (octanol\/water) partition coefficient: Uncertain<\/p>\n
17. Explosion upper limit (%, V\/V): Uncertain<\/p>\n
18. Lower explosion limit (%, V\/V): Uncertain<\/p>\n
19. Solubility: soluble in alcohol and acetone, soluble in hot water, insoluble in benzene and toluene. <\/p>\n<\/p>\n
Acute toxicity:<\/p>\n
Rat caliber LD50: 1500 ug\/kg; rat inhalation LC50: 2 gm\/m3\/4H<\/p>\n
Rat skin LD50: 200mg\/kg; Rat LD50: 11mg\/kg;<\/p>\n
Mouse LD50: 28300 ug\/kg; Mouse LD50: 300mg\/kg<\/p>\n
Dog LD50: 3mg\/kg;<\/p>\n
Cat caliber LD50: 15mg\/kg;<\/p>\n
Rabbit caliber LD50: 35mg\/kg;\uff40<\/p>\n
Pig caliber LD50: 1\uff15mg\/kg;\uff40<\/p>\n
Duck caliber LD50: 3158mg\/kg; <\/p>\n
Breeding animal LD50: 910ug\/kg;\n <\/p>\n
\n None yet\n <\/p>\n
1. Molar refractive index: 96.78<\/p>\n
2. Molar volume (cm3<\/sup>\/mol): 267.3<\/p>\n3. Isotonic specific volume (90.2K ): 731.7<\/p>\n4. Surface tension (dyne\/cm): 56.1<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 38.56<\/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: 3<\/p>\n4. Number of rotatable chemical bonds: 4<\/p>\n5. Number of tautomers: 5<\/p>\n6. Topological molecule polar surface area 51.2<\/p>\n7. Number of heavy atoms: 26<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 512<\/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>\nThe sodium salt (often called diphacin sodium salt) has a solubility of 5% in water at 100\u00b0C. It changes from yellow to red when heated to 207-208\u00b0C and decomposes at 325\u00b0C. <\/p>\n<\/p>\nStorage method<\/h2>\nStored sealed and protected from light. <\/p>\nDuring storage and transportation, it must be protected from moisture and sunlight, kept ventilated, and must not be mixed with food, seeds, or feed.\n <\/p>\nSynthesis method<\/h2>\n1. Preparation of phenylacetone. Industrially, phenylacetamide is used as raw material and reacted at 110-130\u00b0C for 2 hours in the presence of concentrated sulfuric acid to obtain phenylacetic acid. Phenylacetic acid and acetic anhydride react under the catalysis of anhydrous sodium acetate at 140-150\u00b0C for 18 hours. The acetic acid generated continues to steam out. After the reaction, add an appropriate amount of cold water and separate the water layer. The crude phenyl acetone is dissolved in 100% sodium hydroxide with 20% sodium hydroxide. Stir at ~110\u00b0C for 2 hours, and control the pH value to 12. 2. Preparation of diphenyl acetone. Add bromine dropwise into the phenyl acetone mixture, and control the temperature to less than 30\u00b0C to prevent incomplete bromination caused by excessive volatilization of bromine. After the reaction is completed, remove the residual Hydrogen bromide. Then, the generated bromide is added dropwise to the pure benzene liquid under negative pressure, and anhydrous aluminum trichloride is used as the catalyst. The reaction is carried out at room temperature for 3 to 4 hours, and then post-processed to obtain diphenylacetone. 3. Synthesis of diphacin and diphacin sodium salt. Put the solvent toluene and the catalyst sodium methoxide into the reaction pot, raise the temperature to 110\u00b0C, add dimethyl phthalate and toluene mixture after azeotropy, and add diphenyl diphenyl dropwise Add a toluene mixture of acetone and react at 100-120\u00b0C for 1.5-2 hours. In acidic or neutral media, the product obtained is diphacin, and in alkaline medium, diphacin sodium salt is obtained. Sodium methoxide is a strong base, and its amount determines the ratio of the two products (diphacin and diphacin sodium salt). <\/p>\n4.Phenyl acetone is generated from the acylation reaction of phenylacetic acid and acetic anhydride, and phenyl acetone is generated through bromination and phenylation reactions. Diphenyl acetone. Then, the solvent toluene and the catalyst sodium methoxide are put into the reactor, and after azeotropy, a mixture of dimethyl phthalate and toluene is added, and a toluene mixture of partial diphenylacetone is added dropwise. In acidic or neutral media, the product is dimethonium, and in alkaline medium, dimethin sodium salt is obtained. <\/span><\/p>\n<\/p>\nPurpose<\/h2>\n1. Chronic rodenticide. It is the first generation anticoagulant that is widely used. It has broad target spectrum, good palatability, slow action and obvious effect. When a lethal dose is taken, it destroys the hyperthrombin in the blood of rats, prolongs the coagulation time, and causes massive internal bleeding and hypoxia in the rat’s internal organs. Therefore, most rats will run out of the hole before death and become listless and sluggish until they die. Used to kill domestic rats in residences, grain depots, vehicle and ship docks and other places. It can also be used to kill wild rats in dry fields, rice fields, forest areas and grasslands. Use 0.25\u2030~0.5\u2030 poisoning for multiple times in a row. You can also use 1\u2030 poison bait once. Most poisonous baits are prepared with rice or noodles, but you can also use sweet potato shreds, carrot shreds and other baits. For other foods that rats like to eat, add 2% to 5% cooking oil for better results. For example, the preparation of 0.5\u2030 rice bait: Dissolve 0.5g of diphacin sodium salt in an appropriate amount of hot water (above 80\u00b0C), soak it in 1000g of rice to evenly absorb the agent, and dry it to make rice bait. Or dissolve 0.5g of diphacin sodium salt in an appropriate amount of hot water, mix it with 1000g of flour and bake it into dough cakes to make dough bait. <\/p>\n2.It is an anticoagulant rodenticide. It has broad target spectrum, good palatability, slow action and obvious effect. When a lethal dose is taken, it destroys the hyperthrombin in the blood of rats, prolongs the coagulation time, and causes massive internal bleeding and hypoxia in rats until death. Used to kill domestic rats in residences, grain depots, vehicle and ship docks and other places. It can also be used for rodent control in dry fields, rice fields, forest areas and grasslands. Most poisonous baits are prepared with rice or noodles, but sweet potato shreds, carrot shreds and other baits can also be used. <\/span><\/p>\n<\/p>\n extended-reading:https:\/\/www.newtopchem.com\/archives\/64<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat9201-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-c-124-low-odor-tertiary-amine-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2021\/05\/138-3.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/3164-85-0\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat4210-catalyst-cas-683-18-1-dibutyltin-dichloride\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/71.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/coordinated-thiol-methyltin\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40422<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44919<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01T2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48480,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15207],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481"}],"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=48481"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48480"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48481"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48481"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48481"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Isotonic specific volume (90.2K ): 731.7<\/p>\n
4. Surface tension (dyne\/cm): 56.1<\/p>\n
5. Polarizability (10-24<\/sup>cm3<\/sup>): 38.56<\/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: 3<\/p>\n4. Number of rotatable chemical bonds: 4<\/p>\n5. Number of tautomers: 5<\/p>\n6. Topological molecule polar surface area 51.2<\/p>\n7. Number of heavy atoms: 26<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 512<\/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>\nThe sodium salt (often called diphacin sodium salt) has a solubility of 5% in water at 100\u00b0C. It changes from yellow to red when heated to 207-208\u00b0C and decomposes at 325\u00b0C. <\/p>\n<\/p>\nStorage method<\/h2>\nStored sealed and protected from light. <\/p>\nDuring storage and transportation, it must be protected from moisture and sunlight, kept ventilated, and must not be mixed with food, seeds, or feed.\n <\/p>\nSynthesis method<\/h2>\n1. Preparation of phenylacetone. Industrially, phenylacetamide is used as raw material and reacted at 110-130\u00b0C for 2 hours in the presence of concentrated sulfuric acid to obtain phenylacetic acid. Phenylacetic acid and acetic anhydride react under the catalysis of anhydrous sodium acetate at 140-150\u00b0C for 18 hours. The acetic acid generated continues to steam out. After the reaction, add an appropriate amount of cold water and separate the water layer. The crude phenyl acetone is dissolved in 100% sodium hydroxide with 20% sodium hydroxide. Stir at ~110\u00b0C for 2 hours, and control the pH value to 12. 2. Preparation of diphenyl acetone. Add bromine dropwise into the phenyl acetone mixture, and control the temperature to less than 30\u00b0C to prevent incomplete bromination caused by excessive volatilization of bromine. After the reaction is completed, remove the residual Hydrogen bromide. Then, the generated bromide is added dropwise to the pure benzene liquid under negative pressure, and anhydrous aluminum trichloride is used as the catalyst. The reaction is carried out at room temperature for 3 to 4 hours, and then post-processed to obtain diphenylacetone. 3. Synthesis of diphacin and diphacin sodium salt. Put the solvent toluene and the catalyst sodium methoxide into the reaction pot, raise the temperature to 110\u00b0C, add dimethyl phthalate and toluene mixture after azeotropy, and add diphenyl diphenyl dropwise Add a toluene mixture of acetone and react at 100-120\u00b0C for 1.5-2 hours. In acidic or neutral media, the product obtained is diphacin, and in alkaline medium, diphacin sodium salt is obtained. Sodium methoxide is a strong base, and its amount determines the ratio of the two products (diphacin and diphacin sodium salt). <\/p>\n4.Phenyl acetone is generated from the acylation reaction of phenylacetic acid and acetic anhydride, and phenyl acetone is generated through bromination and phenylation reactions. Diphenyl acetone. Then, the solvent toluene and the catalyst sodium methoxide are put into the reactor, and after azeotropy, a mixture of dimethyl phthalate and toluene is added, and a toluene mixture of partial diphenylacetone is added dropwise. In acidic or neutral media, the product is dimethonium, and in alkaline medium, dimethin sodium salt is obtained. <\/span><\/p>\n<\/p>\nPurpose<\/h2>\n1. Chronic rodenticide. It is the first generation anticoagulant that is widely used. It has broad target spectrum, good palatability, slow action and obvious effect. When a lethal dose is taken, it destroys the hyperthrombin in the blood of rats, prolongs the coagulation time, and causes massive internal bleeding and hypoxia in the rat’s internal organs. Therefore, most rats will run out of the hole before death and become listless and sluggish until they die. Used to kill domestic rats in residences, grain depots, vehicle and ship docks and other places. It can also be used to kill wild rats in dry fields, rice fields, forest areas and grasslands. Use 0.25\u2030~0.5\u2030 poisoning for multiple times in a row. You can also use 1\u2030 poison bait once. Most poisonous baits are prepared with rice or noodles, but you can also use sweet potato shreds, carrot shreds and other baits. For other foods that rats like to eat, add 2% to 5% cooking oil for better results. For example, the preparation of 0.5\u2030 rice bait: Dissolve 0.5g of diphacin sodium salt in an appropriate amount of hot water (above 80\u00b0C), soak it in 1000g of rice to evenly absorb the agent, and dry it to make rice bait. Or dissolve 0.5g of diphacin sodium salt in an appropriate amount of hot water, mix it with 1000g of flour and bake it into dough cakes to make dough bait. <\/p>\n2.It is an anticoagulant rodenticide. It has broad target spectrum, good palatability, slow action and obvious effect. When a lethal dose is taken, it destroys the hyperthrombin in the blood of rats, prolongs the coagulation time, and causes massive internal bleeding and hypoxia in rats until death. Used to kill domestic rats in residences, grain depots, vehicle and ship docks and other places. It can also be used for rodent control in dry fields, rice fields, forest areas and grasslands. Most poisonous baits are prepared with rice or noodles, but sweet potato shreds, carrot shreds and other baits can also be used. <\/span><\/p>\n<\/p>\n extended-reading:https:\/\/www.newtopchem.com\/archives\/64<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat9201-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-c-124-low-odor-tertiary-amine-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2021\/05\/138-3.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/3164-85-0\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat4210-catalyst-cas-683-18-1-dibutyltin-dichloride\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/71.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/coordinated-thiol-methyltin\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40422<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44919<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01T2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48480,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15207],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481"}],"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=48481"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48480"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48481"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48481"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48481"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
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: 3<\/p>\n
4. Number of rotatable chemical bonds: 4<\/p>\n
5. Number of tautomers: 5<\/p>\n
6. Topological molecule polar surface area 51.2<\/p>\n
7. Number of heavy atoms: 26<\/p>\n
8. Surface charge: 0<\/p>\n
9. Complexity: 512<\/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
The sodium salt (often called diphacin sodium salt) has a solubility of 5% in water at 100\u00b0C. It changes from yellow to red when heated to 207-208\u00b0C and decomposes at 325\u00b0C. <\/p>\n<\/p>\n
Stored sealed and protected from light. <\/p>\n
During storage and transportation, it must be protected from moisture and sunlight, kept ventilated, and must not be mixed with food, seeds, or feed.\n <\/p>\n
1. Preparation of phenylacetone. Industrially, phenylacetamide is used as raw material and reacted at 110-130\u00b0C for 2 hours in the presence of concentrated sulfuric acid to obtain phenylacetic acid. Phenylacetic acid and acetic anhydride react under the catalysis of anhydrous sodium acetate at 140-150\u00b0C for 18 hours. The acetic acid generated continues to steam out. After the reaction, add an appropriate amount of cold water and separate the water layer. The crude phenyl acetone is dissolved in 100% sodium hydroxide with 20% sodium hydroxide. Stir at ~110\u00b0C for 2 hours, and control the pH value to 12. 2. Preparation of diphenyl acetone. Add bromine dropwise into the phenyl acetone mixture, and control the temperature to less than 30\u00b0C to prevent incomplete bromination caused by excessive volatilization of bromine. After the reaction is completed, remove the residual Hydrogen bromide. Then, the generated bromide is added dropwise to the pure benzene liquid under negative pressure, and anhydrous aluminum trichloride is used as the catalyst. The reaction is carried out at room temperature for 3 to 4 hours, and then post-processed to obtain diphenylacetone. 3. Synthesis of diphacin and diphacin sodium salt. Put the solvent toluene and the catalyst sodium methoxide into the reaction pot, raise the temperature to 110\u00b0C, add dimethyl phthalate and toluene mixture after azeotropy, and add diphenyl diphenyl dropwise Add a toluene mixture of acetone and react at 100-120\u00b0C for 1.5-2 hours. In acidic or neutral media, the product obtained is diphacin, and in alkaline medium, diphacin sodium salt is obtained. Sodium methoxide is a strong base, and its amount determines the ratio of the two products (diphacin and diphacin sodium salt). <\/p>\n
4.Phenyl acetone is generated from the acylation reaction of phenylacetic acid and acetic anhydride, and phenyl acetone is generated through bromination and phenylation reactions. Diphenyl acetone. Then, the solvent toluene and the catalyst sodium methoxide are put into the reactor, and after azeotropy, a mixture of dimethyl phthalate and toluene is added, and a toluene mixture of partial diphenylacetone is added dropwise. In acidic or neutral media, the product is dimethonium, and in alkaline medium, dimethin sodium salt is obtained. <\/span><\/p>\n<\/p>\nPurpose<\/h2>\n1. Chronic rodenticide. It is the first generation anticoagulant that is widely used. It has broad target spectrum, good palatability, slow action and obvious effect. When a lethal dose is taken, it destroys the hyperthrombin in the blood of rats, prolongs the coagulation time, and causes massive internal bleeding and hypoxia in the rat’s internal organs. Therefore, most rats will run out of the hole before death and become listless and sluggish until they die. Used to kill domestic rats in residences, grain depots, vehicle and ship docks and other places. It can also be used to kill wild rats in dry fields, rice fields, forest areas and grasslands. Use 0.25\u2030~0.5\u2030 poisoning for multiple times in a row. You can also use 1\u2030 poison bait once. Most poisonous baits are prepared with rice or noodles, but you can also use sweet potato shreds, carrot shreds and other baits. For other foods that rats like to eat, add 2% to 5% cooking oil for better results. For example, the preparation of 0.5\u2030 rice bait: Dissolve 0.5g of diphacin sodium salt in an appropriate amount of hot water (above 80\u00b0C), soak it in 1000g of rice to evenly absorb the agent, and dry it to make rice bait. Or dissolve 0.5g of diphacin sodium salt in an appropriate amount of hot water, mix it with 1000g of flour and bake it into dough cakes to make dough bait. <\/p>\n2.It is an anticoagulant rodenticide. It has broad target spectrum, good palatability, slow action and obvious effect. When a lethal dose is taken, it destroys the hyperthrombin in the blood of rats, prolongs the coagulation time, and causes massive internal bleeding and hypoxia in rats until death. Used to kill domestic rats in residences, grain depots, vehicle and ship docks and other places. It can also be used for rodent control in dry fields, rice fields, forest areas and grasslands. Most poisonous baits are prepared with rice or noodles, but sweet potato shreds, carrot shreds and other baits can also be used. <\/span><\/p>\n<\/p>\n extended-reading:https:\/\/www.newtopchem.com\/archives\/64<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat9201-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-c-124-low-odor-tertiary-amine-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2021\/05\/138-3.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/3164-85-0\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat4210-catalyst-cas-683-18-1-dibutyltin-dichloride\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/71.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/coordinated-thiol-methyltin\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40422<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44919<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01T2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48480,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15207],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481"}],"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=48481"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48480"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48481"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48481"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48481"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Chronic rodenticide. It is the first generation anticoagulant that is widely used. It has broad target spectrum, good palatability, slow action and obvious effect. When a lethal dose is taken, it destroys the hyperthrombin in the blood of rats, prolongs the coagulation time, and causes massive internal bleeding and hypoxia in the rat’s internal organs. Therefore, most rats will run out of the hole before death and become listless and sluggish until they die. Used to kill domestic rats in residences, grain depots, vehicle and ship docks and other places. It can also be used to kill wild rats in dry fields, rice fields, forest areas and grasslands. Use 0.25\u2030~0.5\u2030 poisoning for multiple times in a row. You can also use 1\u2030 poison bait once. Most poisonous baits are prepared with rice or noodles, but you can also use sweet potato shreds, carrot shreds and other baits. For other foods that rats like to eat, add 2% to 5% cooking oil for better results. For example, the preparation of 0.5\u2030 rice bait: Dissolve 0.5g of diphacin sodium salt in an appropriate amount of hot water (above 80\u00b0C), soak it in 1000g of rice to evenly absorb the agent, and dry it to make rice bait. Or dissolve 0.5g of diphacin sodium salt in an appropriate amount of hot water, mix it with 1000g of flour and bake it into dough cakes to make dough bait. <\/p>\n
2.It is an anticoagulant rodenticide. It has broad target spectrum, good palatability, slow action and obvious effect. When a lethal dose is taken, it destroys the hyperthrombin in the blood of rats, prolongs the coagulation time, and causes massive internal bleeding and hypoxia in rats until death. Used to kill domestic rats in residences, grain depots, vehicle and ship docks and other places. It can also be used for rodent control in dry fields, rice fields, forest areas and grasslands. Most poisonous baits are prepared with rice or noodles, but sweet potato shreds, carrot shreds and other baits can also be used. <\/span><\/p>\n<\/p>\n extended-reading:https:\/\/www.newtopchem.com\/archives\/64<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat9201-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-c-124-low-odor-tertiary-amine-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2021\/05\/138-3.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/3164-85-0\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat4210-catalyst-cas-683-18-1-dibutyltin-dichloride\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/71.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/coordinated-thiol-methyltin\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40422<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44919<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01T2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48480,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15207],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481"}],"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=48481"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48480"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48481"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48481"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48481"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
extended-reading:https:\/\/www.newtopchem.com\/archives\/64<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat9201-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-c-124-low-odor-tertiary-amine-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2021\/05\/138-3.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/3164-85-0\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat4210-catalyst-cas-683-18-1-dibutyltin-dichloride\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/71.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/coordinated-thiol-methyltin\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40422<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44919<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01T2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48480,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15207],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481"}],"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=48481"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48480"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48481"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48481"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48481"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Structural formula Business number 01T2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48480,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15207],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481"}],"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=48481"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48481\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48480"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48481"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48481"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48481"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
![\"Diphenylindone](\"http:\/\/www.newtopchem.com\/wp-content\/uploads\/2024\/05\/1afdd09f3ea14d2dbed1c9e6fbd1e948.gif\")
<\/p>\n<\/p>\n![https:\/\/www.bdmaee.net\/wp-content\/uploads\/2021\/05\/138-3.jpg<\/a><\/br>extended-reading:](\"https:\/\/www.bdmaee.net\/wp-content\/uploads\/2021\/05\/138-3.jpg\"){kind=link}
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