U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C19H24N2.ClH
Molecular Weight 316.868
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IMIPRAMINE HYDROCHLORIDE

SMILES

Cl.CN(C)CCCN1C2=C(CCC3=C1C=CC=C3)C=CC=C2

InChI

InChIKey=XZZXIYZZBJDEEP-UHFFFAOYSA-N
InChI=1S/C19H24N2.ClH/c1-20(2)14-7-15-21-18-10-5-3-8-16(18)12-13-17-9-4-6-11-19(17)21;/h3-6,8-11H,7,12-15H2,1-2H3;1H

HIDE SMILES / InChI
Molecular Formula C19H24N2
Molecular Weight 280.4073
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:12:28 UTC 2023
Edited
by admin
on Fri Dec 15 15:12:28 UTC 2023
Record UNII
BKE5Q1J60U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IMIPRAMINE HYDROCHLORIDE
EP   MART.   MI   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD   WHO-IP  
Common Name English
IMIPRAMINE HYDROCHLORIDE [USP-RS]
Common Name English
IMIPRAMINE HYDROCHLORIDE [MI]
Common Name English
IMIPRAMINE HYDROCHLORIDE [USP IMPURITY]
Common Name English
IMIZINE
Common Name English
IMIDOBENZYLE
Common Name English
TOFRANIL
Common Name English
Imipramine hydrochloride [WHO-DD]
Common Name English
IMIPRAMINI HYDROCHLORIDUM [WHO-IP LATIN]
Common Name English
IMIPRAMINE HYDROCHLORIDE [MART.]
Common Name English
NSC-114900
Code English
PRAMINE
Brand Name English
PRYLEUGAN
Common Name English
PRESAMINE
Brand Name English
5-(3-(DIMETHYLAMINO)PROPYL)-10,11-DIHYDRO-5H-DIBENZ(B,F)AZEPINE MONOHYDROCHLORIDE
Systematic Name English
IMIPRAMINE HCL
Common Name English
JANIMINE
Brand Name English
IMIPRAMINE HYDROCHLORIDE [USP MONOGRAPH]
Common Name English
IMIPRAMINE HYDROCHLORIDE [VANDF]
Common Name English
IMIPRAMINE HYDROCHLORIDE [ORANGE BOOK]
Common Name English
5H-DIBENZ(B,F)AZEPINE-5-PROPANAMINE, 10,11-DIHYDRO-N,N-DIMETHYL-, MONOHYDROCHLORIDE
Common Name English
IMIPRAMINE HYDROCHLORIDE [JAN]
Common Name English
IMIPRAMINE HYDROCHLORIDE [EP MONOGRAPH]
Common Name English
G-22355
Code English
IMIPRAMINE HYDROCHLORIDE [WHO-IP]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C94727
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
Code System Code Type Description
SMS_ID
100000092315
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
ECHA (EC/EINECS)
204-030-7
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
MERCK INDEX
m6232
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY Merck Index
CHEBI
47499
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
EPA CompTox
DTXSID7040738
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
ChEMBL
CHEMBL11
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
EVMPD
SUB02644MIG
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
CAS
113-52-0
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
DRUG BANK
DBSALT000099
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
NCI_THESAURUS
C29116
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
PUBCHEM
8228
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
FDA UNII
BKE5Q1J60U
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
NSC
114900
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
CHEBI
5882
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
IMIPRAMINE HYDROCHLORIDE
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY Description: A white or slightly yellowish, crystalline powder; odourless or almost odourless. Solubility: Freely soluble in water, ethanol (~750 g/l) TS; practically insoluble in ether R. Category: Psychotherapeutic drug. Storage: Imipramine hydrochloride should be kept in a tightly closed container, protected from light. Additional information: Even in the absence of light, Imipramine hydrochloride is gradually degraded on exposure to a humid atmosphere, the decomposition being faster at higher temperatures.Requirement: Imipramine hydrochloride contains not less than 98.0% and not more than the equivalent of 102.0% of C19H24N2,HCl, calculated with reference to the dried substance.
DAILYMED
BKE5Q1J60U
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
RS_ITEM_NUM
1338007
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY
RXCUI
150816
Created by admin on Fri Dec 15 15:12:28 UTC 2023 , Edited by admin on Fri Dec 15 15:12:28 UTC 2023
PRIMARY RxNorm
Related Record Type Details
Structure of IMIPRAMINE HYDROCHLORIDE
BASIS OF STRENGTH->SUBSTANCE
ASSAY (HPLC)
USP
Structure of IMIPRAMINE
PARENT -> SALT/SOLVATE
Structure of IMIPRAMINE HYDROCHLORIDE
BASIS OF STRENGTH->SUBSTANCE
ASSAY (TITRATION)
EP
Related Record Type Details
Structure of DEPRAMINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
Structure of IMIPRAMINE
ACTIVE MOIETY
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966