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NORTRIPTYLINE

CAS No.
72-69-5
Chemical Name:
NORTRIPTYLINE
Synonyms
Aventyl;nortryptyline;C07274;Ateben;Sesaval;Avantyl;lambeck;Lumbeck;Noritren;allegron
CBNumber:
CB1317147
Molecular Formula:
C19H21N
Molecular Weight:
263.38
MDL Number:
MFCD00242775
MOL File:
72-69-5.mol
Last updated:2023-09-05 17:53:06

NORTRIPTYLINE Properties

Melting point 58 °C
Boiling point 396.62°C (rough estimate)
Density 0.9790 (rough estimate)
refractive index 1.4900 (estimate)
storage temp. 4°C, protect from light
pka pKa 9.7 (Uncertain)
BCS Class 1
NCI Dictionary of Cancer Terms Aventyl; nortriptyline
FDA UNII BL03SY4LXB
ATC code N06AA10
EPA Substance Registry System Nortriptyline (72-69-5)

Pharmacokinetic data

Protein binding 95%
Excreted unchanged in urine <5%
Volume of distribution 15-23(L/kg)
Biological half-life 25-38 / 15-66

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P330-P501
Toxicity LD50 orl-rat: 502 mg/kg HEPHD2 55,527,80

NORTRIPTYLINE price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Usbiological N4005-02 Nortriptyline 72-69-5 500ul $393 2021-12-16 Buy
American Custom Chemicals Corporation API0003635 NORTRIPTYLINE 95.00% 72-69-5 500MG $742 2021-12-16 Buy
American Custom Chemicals Corporation API0003635 NORTRIPTYLINE 95.00% 72-69-5 1G $756 2021-12-16 Buy
Product number Packaging Price Buy
N4005-02 500ul $393 Buy
API0003635 500MG $742 Buy
API0003635 1G $756 Buy

NORTRIPTYLINE Chemical Properties,Uses,Production

Originator

Aventyl,Lilly,UK,1963

Uses

Antidepressant.

Uses

Nortriptyline is a drug with a relatively short latent period of action. It is practically devoid of sedative effects. It is used in manic-depressive psychoses, in all forms of endogenous depression, and also in major depressive conditions.

Definition

ChEBI: An organic tricyclic compound that is 10,11-dihydro-5H-dibenzo[a,d][7]annulene substituted by a 3-(methylamino)propylidene group at position 5. It is an active metabolite of amitriptyline.

Manufacturing Process

A mixture of 114.5 g of 5-(3-chloropropylidene)dibenzo[a,d]cyclohepta[1,4] diene, 75 ml of benzene, and about 400 ml of methylamine is heated in an autoclave at 120°C for six hours. The excess methylamine is distilled from the reaction mixture under vacuum and the residue is stirred with 300 ml of water. Acidification of the mixture with hydrochloric acid causes the separation of the hydrochloride of 5-(3-methylaminopropylidene)dibenzo[a,d] cyclohepta[1,4]diene. The product is collected by filtration and is purified by recrystallization from a mixture of absolute ethanol and ethyl acetate. MP 210°C to 212°C.

brand name

Aventyl Hydrochloride (Lilly); Aventyl Hydrochloride (Ranbaxy); Pamelor (Tyco).

Therapeutic Function

Antidepressant

Clinical Use

Tricyclic antidepressant

Safety Profile

Poison by ingestion,intraperitoneal, and intravenous routes. When heated todecomposition it emits toxic fumes of NOx.

Synthesis

Nortriptyline is 5-(3-methylaminopropyliden)-10,11-dihydrodibenzcycloheptene (7.1.17). Nortriptyline differs from desipramine in the same manner in which amitriptyline differs from imipramine. In nortriptyline, the nitrogen atom in the central part of the tricyclic system of desipramine is replaced by a carbon atom, which is bound to a side chain by a double bond.
Two suggested methods of nortriptyline synthesis are based on the N-demethylation of amitriptyline. The third way utilizes the reaction of methylamine with 5-(3-bromopropyliden)-10,11-dihydro-5H-dibenz[a,d]cycloheptene (7.1.18).
According to the first scheme, demethylation takes place by the reaction of amitriptyline (7.1.4) with methyliodide, which leads to the formation of a quaternary ammonium salt (7.1.16), the reaction of which with methylamine at a relatively high temperature gives the desired nortriptyline (7.1.17) [25].
Synthesis_72-69-5_1
According to the third scheme, nortriptyline is synthesized by reacting methylamine with 5-(3-bromopropyliden)-10,11-dihydro-5H-dibenz[a,d]cycloheptene (7.1.6) [8].
Synthesis_72-69-5_2

Drug interactions

Potentially hazardous interactions with other drugs
Alcohol: increased sedative effect.
Analgesics: increased risk of CNS toxicity with tramadol; possibly increased risk of side effects with nefopam; possibly increased sedative effects with opioids.
Anti-arrhythmics: increased risk of ventricular arrhythmias with amiodarone - avoid; increased risk of ventricular arrhythmias with disopyramide, flecainide or propafenone; avoid with dronedarone.
Antibacterials: increased risk of ventricular arrhythmias with delamanid, moxifloxacin and possibly telithromycin - avoid with moxifloxacin.
Anticoagulants: may alter anticoagulant effect of coumarins.
Antidepressants: enhanced CNS excitation and hypertension with MAOIs and moclobemide - avoid; concentration possibly increased with SSRIs; risk of ventricular arrhythmias with citalopram and escitalopram - avoid; increased risk of convulsions with vortioxetine.
Antiepileptics: convulsive threshold lowered; concentration reduced by carbamazepine, fosphenytoin, phenobarbital and possibly phenytoin.
Antimalarials: avoid with artemether/lumefantrine and piperaquine with artenimol.
Antipsychotics: increased risk of ventricular arrhythmias especially with droperidol, haloperidol, pimozide, risperidone and sulpiride - avoid; increased antimuscarinic effects with clozapine and phenothiazines; concentration increased by antipsychotics.
Antivirals: increased risk of ventricular arrhythmias with saquinavir - avoid; concentration possibly increased with ritonavir.
Atomoxetine: increased risk of ventricular arrhythmias and possibly convulsions.
Beta-blockers: increased risk of ventricular arrhythmias with sotalol.
Clonidine: tricyclics antagonise hypotensive effect; increased risk of hypertension on clonidine withdrawal.
Dapoxetine: possible increased risk of serotonergic effects - avoid.
Dopaminergics: avoid use with entacapone; CNS toxicity reported with selegiline and rasagiline.
Pentamidine: increased risk of ventricular arrhythmias.
Sympathomimetics: increased risk of hypertension and arrhythmias with adrenaline and noradrenaline; metabolism possibly inhibited by methylphenidate.

Metabolism

Nortriptyline is a secondary amine dibenzocycloheptene TCA as well as the major metabolite of amitriptyline. Similar to desipramine, nortriptyline appears in mother's milk and is metabolized by CYP2D6 to the primary amine and by ring hydroxylation to its E-10-hydroxy metabolite. Approximately one-third of a dose of nortriptyline is excreted in urine as metabolites within 24 hours, and small amounts are excreted in feces via biliary elimination.

NORTRIPTYLINE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 44)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Yanxi Chemical Co., Ltd.
+8617531190177 peter@yan-xi.com China 5993 58
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9348 55
SHANDONG ZHI SHANG CHEMICAL CO.LTD
+86 18953170293 sales@sdzschem.com China 2931 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Career Henan Chemica Co
+86-0371-86658258 15093356674; laboratory@coreychem.com China 30255 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29271 58
AFINE CHEMICALS LIMITED
0571-85134551 info@afinechem.com CHINA 15377 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923 1026@dideu.com China 9116 58
Hebei Duling International Trade Co. LTD
+8618032673083 sales05@hbduling.cn China 15745 58

View Lastest Price from NORTRIPTYLINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
nortriptyline pictures 2023-09-05 nortriptyline
72-69-5
US $50.00 / kg 1kg 0.99 20tons Hebei Yanxi Chemical Co., Ltd.
NORTRIPTYLINE USP/EP/BP pictures 2021-07-27 NORTRIPTYLINE USP/EP/BP
72-69-5
US $1.10 / g 1g 99.9% 100 Tons min Dideu Industries Group Limited
  • nortriptyline pictures
  • nortriptyline
    72-69-5
  • US $50.00 / kg
  • 0.99
  • Hebei Yanxi Chemical Co., Ltd.
5-(alpha-methylaminopropylidene)dibenzo[a,d]cyclohepta[1,4]diene 5-[3-(Methylamino)propylidene]dibenzo[a,E]cyclohepta[1,5]diene Noramitriptyline Noritren Nortryptiline Psychostyl Sesaval NORTRIPTYLINE N-[3-(10,11-DIHYDRO-5H-DIBENZO[A,D][7]ANNULEN-5-YLIDENE)PROPYL]-N-METHYLAMINE HYDROCHLORIDE 10,11-dihydro-5-(3-methylaminopropylidene)dibenzo(a,d)cycloheptene demethylamitryptylene demethyl-amitryptylin Demethylamitryptyline Desitriptilina Desmethylamitriptyline 10,11-dihydro-5-(3-methylaminopropylidene)-5h-dibenzo[a,d][1,4]cycloheptene 10,11-Dihydro-N-methyl-5H-dibenzo(a,d)cycloheptane-delta,gamma-propylamine 10,11-dihydro-n-methyl-5h-dibenzo(a,d)cycloheptene-delta(5,gamma)-propylamin 10,11-dihydro-n-methyl-5h-dibenzo[a,d]cycloheptene-delta(5,gamma)-propylamine 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl- 1-propanamine,3-(10,11-dihydro-5h-dibenzo(a,d)cycloheptene-5-ylidene)-n-methyl Nortrityline C07274 5h-dibenzo(a,d)cycloheptene-delta(5,gamma)-propylamine,10,11-dihydro-n-methyl 5H-Dibenzo[a,d]cycloheptene-delta5,gamma-propylamine, 10,11-dihydro-N-methyl- allegron Amitryptyline, demethyl- Ateben Avantyl Demethylamitriptylene Demethylamitriptyline 3-(10,11-dihydro-5h-dibenzo[a,d]-cyclohepten-5-ylidene)-n-methyl-1-propanamine 3-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-1-propanamine 3-(10,11-dihydro-5h-dibenzo[a,d]cyclohepten-5-ylidene)-n-methylpropylamine 5-(3-(methylamino)propylidene)dibenzo(a,e)cyclohepta(1,5)diene 5-(3-Methylaminopropylidene)-10,11-dihydro-5H-dibenzo(a,d)cycloheptene lambeck Lumbeck Amitriptyline EP Impurity C NORTRIPTYLINE USP/EP/BP nortryptyline Aventyl Nortriptylene c.3-(10,11-dihydro-5h-dibenzo[a,d][7]annulen-5-ylidene)-N-methylpropan-1-amine(nortriptyline), 72-69-5 84-71-3