{"id":48846,"date":"2024-05-16T18:01:48","date_gmt":"2024-05-16T10:01:48","guid":{"rendered":"http:\/\/www.newtopchem.com\/archives\/48846"},"modified":"2024-05-16T18:01:48","modified_gmt":"2024-05-16T10:01:48","slug":"nortriptyline","status":"publish","type":"post","link":"http:\/\/www.newtopchem.com\/archives\/48846","title":{"rendered":"nortriptyline","gt_translate_keys":[{"key":"rendered","format":"text"}]},"content":{"rendered":"

$\"Nortriptyline$ <\/p>\n

Structural formula<\/p>\n\n\n\n\n\n\n\n
Business number<\/th>\n 01H8<\/td>\n<\/tr>\n
Molecular formula<\/th>\n C19H21N<\/td>\n<\/tr>\n
Molecular weight<\/th>\n 263.38<\/td>\n<\/tr>\n
label<\/th>\n \n
10,11-dihydro-5-(3-methylaminopropylidene)-5h-dibenzo[a,d][1,4]cycloheptene,<\/p>\n
3-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-1-propanamine<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
\n
Numbering system<\/a><\/li>\n
Physical property data<\/a><\/li>\n
Toxicological data<\/a><\/li>\n
Ecological data<\/a><\/li>\n
Molecular structure data<\/a><\/li>\n
Computing chemical data<\/a><\/li>\n
\n More <\/span><\/a><\/p>\n
\n
Properties and Stability<\/a><\/li>\n
Storage method<\/a><\/li>\n
Synthesis method<\/a><\/li>\n
Purpose<\/a><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n
Numbering system<\/h2>\n
CAS number:<\/b>72-69-5<\/p>\n
MDL number:<\/b>None<\/p>\n
EINECS number:<\/b>200-788-8<\/p>\n
RTECS number:<\/b>None<\/p>\n
BRN number:<\/b>None<\/p>\n
PubChem ID:<\/b>None<\/p>\n
Physical property data<\/h2>\n
\n
<\/SPAN><\/SPAN> <\/P>\n <\/p>\n
Toxicological data<\/h2>\n
\n
Acute toxicity: Rat oral LD50<\/SPAN>: 502 mg\/kg<\/SPAN>; Rat intravenous LD50 <\/SPAN>: 22 mg\/kg<\/SPAN>; <\/SPAN><\/SPAN><\/P>
\n
<\/SPAN><\/SPAN>Mouse oral administration LD50<\/SPAN>: 370 mg\/kg<\/SPAN>; Mouse abdominal cavity LD50<\/SPAN>: 70 mg\/kg<\/SPAN>; Mouse VeinLD50<\/SPAN>\uff1a17 mg\/kg<\/SPAN>; <\/SPAN><\/SPAN><\/SPAN><\/P>\n <\/p>\n
Ecological data<\/h2>\n
\n None\n <\/p>\n
Molecular structure data<\/h2>\n
\n
1. <\/SPAN><\/SPAN><\/SPAN>Molar refractive index:<\/SPAN>86.76<\/SPAN><\/P>
\n
2. <\/SPAN><\/SPAN><\/SPAN>Molar volume (<\/SPAN>m^{3<\/SUP>\/mol<\/SPAN>\uff09\uff1a<\/SPAN>242.8<\/SPAN><\/P>
\n}
3. <\/SPAN><\/SPAN><\/SPAN>isotonic specific volume (<\/SPAN>90.2K<\/SPAN>):<\/SPAN>636.9<\/SPAN><\/P>
\n
4. <\/SPAN><\/SPAN><\/SPAN>Surface Tension (<\/SPAN>dyne\/cm<\/SPAN>):<\/SPAN>47.3<\/SPAN><\/P>
\n
5. <\/SPAN><\/SPAN><\/SPAN>Polarizability<\/SPAN>\uff08<\/SPAN>10^{-24<\/SUP>cm^{3<\/SUP><\/SPAN>):<\/SPAN>34.39<\/SPAN><\/P>\n <\/p>\n}}
Compute chemical data<\/h2>\n
1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n
2. Number of hydrogen bond donors: 1<\/p>\n
3. Number of hydrogen bond acceptors: 1<\/p>\n
4. Number of rotatable chemical bonds: 3<\/p>\n
5. Number of tautomers: none<\/p>\n
6. Topological molecule polar surface area 12<\/p>\n
7. Number of heavy atoms: 20<\/p>\n
8. Surface charge: 0<\/p>\n
9. Complexity: 307<\/p>\n
10. Number of isotope atoms: 0<\/p>\n
11. Determine the number of atomic stereocenters: 0<\/p>\n
12. The number of uncertain stereocenters of atoms: 0<\/p>\n
13. The number of determined stereocenters of chemical bonds: 0<\/p>\n
14. The number of uncertain stereocenters of chemical bonds: 0<\/p>\n
15. Number of covalent bond units: 1<\/p>\n<\/p>\n
Properties and stability<\/h2>\n
\n None\n <\/p>\n
Storage method<\/h2>\n
\n None\n <\/p>\n
Synthesis method<\/h2>\n
\n None\n <\/p>\n
Purpose<\/h2>\n
\n None\n <\/p>\n
extended-reading:https:\/\/www.newtopchem.com\/archives\/1031<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/jeffcat-zr-70-catalyst-cas1704-62-7-huntsman\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-90-72-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-b-18-tertiary-amine-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-polycat-9-tertiary-amine-catalyst-polycat-9\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/strong-gel-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-nem-niax-nem-jeffcat-nem\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/dimethomorph\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5387\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/39796<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"
Structural formula Business number 01H8 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48845,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15322],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48846"}],"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=48846"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48846\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48845"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48846"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48846"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48846"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}

Business number<\/th>\n	01H8<\/td>\n<\/tr>\n
Molecular formula<\/th>\n	C19H21N<\/td>\n<\/tr>\n
Molecular weight<\/th>\n	263.38<\/td>\n<\/tr>\n
label<\/th>\n	\n 10,11-dihydro-5-(3-methylaminopropylidene)-5h-dibenzo[a,d][1,4]cycloheptene,<\/p>\n 3-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-1-propanamine<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n \n Numbering system<\/a><\/li>\n Physical property data<\/a><\/li>\n Toxicological data<\/a><\/li>\n Ecological data<\/a><\/li>\n Molecular structure data<\/a><\/li>\n Computing chemical data<\/a><\/li>\n \n More <\/span><\/a><\/p>\n \n Properties and Stability<\/a><\/li>\n Storage method<\/a><\/li>\n Synthesis method<\/a><\/li>\n Purpose<\/a><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n Numbering system<\/h2>\n CAS number:<\/b>72-69-5<\/p>\n MDL number:<\/b>None<\/p>\n EINECS number:<\/b>200-788-8<\/p>\n RTECS number:<\/b>None<\/p>\n BRN number:<\/b>None<\/p>\n PubChem ID:<\/b>None<\/p>\n Physical property data<\/h2>\n \n <\/SPAN><\/SPAN> <\/P>\n <\/p>\n Toxicological data<\/h2>\n \n Acute toxicity: Rat oral LD50<\/SPAN>: 502 mg\/kg<\/SPAN>; Rat intravenous LD50 <\/SPAN>: 22 mg\/kg<\/SPAN>; <\/SPAN><\/SPAN><\/P> \n <\/SPAN><\/SPAN>Mouse oral administration LD50<\/SPAN>: 370 mg\/kg<\/SPAN>; Mouse abdominal cavity LD50<\/SPAN>: 70 mg\/kg<\/SPAN>; Mouse VeinLD50<\/SPAN>\uff1a17 mg\/kg<\/SPAN>; <\/SPAN><\/SPAN><\/SPAN><\/P>\n <\/p>\n Ecological data<\/h2>\n \n None\n <\/p>\n Molecular structure data<\/h2>\n \n 1. <\/SPAN><\/SPAN><\/SPAN>Molar refractive index:<\/SPAN>86.76<\/SPAN><\/P> \n 2. <\/SPAN><\/SPAN><\/SPAN>Molar volume (<\/SPAN>m^{3<\/SUP>\/mol<\/SPAN>\uff09\uff1a<\/SPAN>242.8<\/SPAN><\/P> \n} 3. <\/SPAN><\/SPAN><\/SPAN>isotonic specific volume (<\/SPAN>90.2K<\/SPAN>):<\/SPAN>636.9<\/SPAN><\/P> \n 4. <\/SPAN><\/SPAN><\/SPAN>Surface Tension (<\/SPAN>dyne\/cm<\/SPAN>):<\/SPAN>47.3<\/SPAN><\/P> \n 5. <\/SPAN><\/SPAN><\/SPAN>Polarizability<\/SPAN>\uff08<\/SPAN>10^{-24<\/SUP>cm^{3<\/SUP><\/SPAN>):<\/SPAN>34.39<\/SPAN><\/P>\n <\/p>\n}} Compute chemical data<\/h2>\n 1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n 2. Number of hydrogen bond donors: 1<\/p>\n 3. Number of hydrogen bond acceptors: 1<\/p>\n 4. Number of rotatable chemical bonds: 3<\/p>\n 5. Number of tautomers: none<\/p>\n 6. Topological molecule polar surface area 12<\/p>\n 7. Number of heavy atoms: 20<\/p>\n 8. Surface charge: 0<\/p>\n 9. Complexity: 307<\/p>\n 10. Number of isotope atoms: 0<\/p>\n 11. Determine the number of atomic stereocenters: 0<\/p>\n 12. The number of uncertain stereocenters of atoms: 0<\/p>\n 13. The number of determined stereocenters of chemical bonds: 0<\/p>\n 14. The number of uncertain stereocenters of chemical bonds: 0<\/p>\n 15. Number of covalent bond units: 1<\/p>\n<\/p>\n Properties and stability<\/h2>\n \n None\n <\/p>\n Storage method<\/h2>\n \n None\n <\/p>\n Synthesis method<\/h2>\n \n None\n <\/p>\n Purpose<\/h2>\n \n None\n <\/p>\n extended-reading:https:\/\/www.newtopchem.com\/archives\/1031<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/jeffcat-zr-70-catalyst-cas1704-62-7-huntsman\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-90-72-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-b-18-tertiary-amine-catalyst-momentive\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-polycat-9-tertiary-amine-catalyst-polycat-9\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/strong-gel-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-nem-niax-nem-jeffcat-nem\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/dimethomorph\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5387\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/39796<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":" Structural formula Business number 01H8 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48845,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15322],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48846"}],"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=48846"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48846\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48845"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48846"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48846"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48846"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}

Numbering system<\/h2>\nCAS number:<\/b>72-69-5<\/p>\nMDL number:<\/b>None<\/p>\nEINECS number:<\/b>200-788-8<\/p>\nRTECS number:<\/b>None<\/p>\nBRN number:<\/b>None<\/p>\nPubChem ID:<\/b>None<\/p>\n

Ecological data<\/h2>\n\n None\n <\/p>\n

Properties and stability<\/h2>\n\n None\n <\/p>\n

Storage method<\/h2>\n\n None\n <\/p>\n

Synthesis method<\/h2>\n\n None\n <\/p>\n

Numbering system<\/h2>\n
CAS number:<\/b>72-69-5<\/p>\n
MDL number:<\/b>None<\/p>\n
EINECS number:<\/b>200-788-8<\/p>\n
RTECS number:<\/b>None<\/p>\n
BRN number:<\/b>None<\/p>\n
PubChem ID:<\/b>None<\/p>\n

Ecological data<\/h2>\n
\n None\n <\/p>\n

Properties and stability<\/h2>\n
\n None\n <\/p>\n

Storage method<\/h2>\n
\n None\n <\/p>\n

Synthesis method<\/h2>\n
\n None\n <\/p>\n