Nortriptyline

Modify Date: 2025-08-25 00:53:30

Nortriptyline Structure
Nortriptyline structure
Common Name Nortriptyline
CAS Number 72-69-5 Molecular Weight 263.37700
Density 1.084 g/cm3 Boiling Point 403.4ºC at 760 mmHg
Molecular Formula C19H21N Melting Point N/A
MSDS N/A Flash Point 194.9ºC

 Use of Nortriptyline


Nortriptyline (Desmethylamitriptyline), the main active metabolite of Amitriptyline, is a tricyclic antidepressant used to relieve the symptoms of depression. Nortriptyline is a potent autophagy inhibitor[1][2].

 Names

Name nortriptyline
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.084 g/cm3
Boiling Point 403.4ºC at 760 mmHg
Molecular Formula C19H21N
Molecular Weight 263.37700
Flash Point 194.9ºC
Exact Mass 263.16700
PSA 12.03000
LogP 4.21730
Index of Refraction 1.633
InChIKey PHVGLTMQBUFIQQ-UHFFFAOYSA-N
SMILES CNCCC=C1c2ccccc2CCc2ccccc21
Storage condition 2-8°C

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
HO9800000
CHEMICAL NAME :
5H-Dibenzo(a,d)cycloheptene-delta(sup 5),gamma-propylamine, 10,11-dihydro-N-methyl-
CAS REGISTRY NUMBER :
72-69-5
LAST UPDATED :
199707
DATA ITEMS CITED :
8
MOLECULAR FORMULA :
C19-H21-N
MOLECULAR WEIGHT :
263.41
WISWESSER LINE NOTATION :
L C676 BY&T&J BU3M1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
502 mg/kg
TOXIC EFFECTS :
Behavioral - muscle weakness Behavioral - ataxia Behavioral - muscle contraction or spasticity
REFERENCE :
HEPHD2 Handbook of Experimental Pharmacology. (Springer-Verlag, Heidelberger Pl. 3, D-1000 Berlin 33, Fed. Rep. Ger.) V.50- 1978- Volume(issue)/page/year: 55,527,1980
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
22 mg/kg
TOXIC EFFECTS :
Behavioral - muscle weakness Behavioral - ataxia Behavioral - muscle contraction or spasticity
REFERENCE :
HEPHD2 Handbook of Experimental Pharmacology. (Springer-Verlag, Heidelberger Pl. 3, D-1000 Berlin 33, Fed. Rep. Ger.) V.50- 1978- Volume(issue)/page/year: 55,527,1980
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
370 mg/kg
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity)
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 20,1561,1970
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
70 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JMCMAR Journal of Medicinal Chemistry. (American Chemical Soc., Distribution Office Dept. 223, POB POB 57136, West End Stn., Washington, DC 20037) V.6- 1963- Volume(issue)/page/year: 6,338,1963
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
17 mg/kg
TOXIC EFFECTS :
Behavioral - changes in motor activity (specific assay)
REFERENCE :
JMCMAR Journal of Medicinal Chemistry. (American Chemical Soc., Distribution Office Dept. 223, POB POB 57136, West End Stn., Washington, DC 20037) V.6- 1963- Volume(issue)/page/year: 17,65,1974 *** REVIEWS *** TOXICOLOGY REVIEW DICPBB Drug Intelligence and Clinical Pharmacy. (POB 42435, Cincinnati, OH 45242) V.3- 1969- Volume(issue)/page/year: 8,690,1974 TOXICOLOGY REVIEW CLCHAU Clinical Chemistry (Winston-Salem, NC). (American Assoc. for Clinical Chemistry, 1725 K St., NW, Washington, DC 20006) V.1- 1955- Volume(issue)/page/year: 19,361,1973 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X4842 No. of Facilities: 25 (estimated) No. of Industries: 1 No. of Occupations: 1 No. of Employees: 2440 (estimated) No. of Female Employees: 1459 (estimated)

 Safety Information

HS Code 2921499090

 Synthetic Route

 Customs

HS Code 2921499090
Summary 2921499090 other aromatic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

 NortriptylineBioassay

View more

Name: Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression
Source: NCGC
External Id: SNCA-p-activity-luciferase
Name: pKa (acid-base dissociation constant) as determined by Avdeef ref: DOI: 10.1002/04714...
Source: ChEMBL
Target: N/A
External Id: CHEMBL2449007
Name: Half life period is estimated
Source: ChEMBL
Target: N/A
External Id: CHEMBL633422
Name: Increase the activity of the Burkholderia fixLJ 2-component system
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: Burkholderia multivorans
External Id: HMS1625
Name: pKa (acid-base dissociation constant) as determined by Luan ref: Pharm. Res. 2005
Source: ChEMBL
Target: N/A
External Id: CHEMBL2449009
Name: Apparent partition coefficient was measured as histamine releasing activity in rat ma...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL797214
Name: Lipophilicity, log D at pH7.4
Source: ChEMBL
Target: N/A
External Id: CHEMBL895152
Name: Drug activation in human Hep3B cells assessed as human CYP3A4-mediated drug metabolis...
Source: ChEMBL
Target: Cytochrome P450 3A4
External Id: CHEMBL4479035
Name: Acid dissociation constant, pKa of the compound
Source: ChEMBL
Target: N/A
External Id: CHEMBL895153
Name: Displacement of [3H]LSD from human 5HT6 receptor expressed in HEK293 cells after 1.5 ...
Source: ChEMBL
Target: 5-hydroxytryptamine receptor 6
External Id: CHEMBL2157129
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 Synonyms

Sesaval
Lumbeck
NORTRIPTYLINE
Ateben
noramitriptyline
Noritren
allegron
[14C]-Nortriptyline
desmethylamitriptyline
lambeck
EINECS 200-788-8
Aventyl
Psychostyl
notriptyline
Avantyl
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