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Verapamil hydrochloride_Molecular_structure_CAS_152-11-4)
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Verapamil hydrochloride

Catalog No. 381195 Name Sigma Aldrich
CAS Number 152-11-4 Website http://www.sigmaaldrich.com
M. F. C27H39ClN2O4 Telephone 1-800-521-8956
M. W. 491.06256 Fax
Purity 98% Email
Storage Chembase ID: 53601

SYNONYMS

IUPAC name
2-(3,4-dimethoxyphenyl)-5-{[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino}-2-(propan-2-yl)pentanenitrile hydrochloride
IUPAC Traditional name
veraβ hydrochloride
Synonyms
5-[N-(3,4-Dimethoxyphenylethyl)methylamino]-2-(3,4-dimethoxyphenyl)-2-isopropylvaleronitrile hydrochloride
(±)-Verapamil hydrochloride

DATABASE IDS

EC Number 205-800-5
CAS Number 152-11-4
Beilstein Number 3647093
MDL Number MFCD00055208
PubChem SID 24863792

PROPERTIES

Linear Formula (CH3O)2C6H3CH2CH2N(CH3)(CH2)3C[C6H3(OCH3)2][CH(CH3)2]CN · HCl
Purity 98%
Melting Point 142 °C (dec.)(lit.)
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H301-H311-H331
European Hazard Symbols Toxic Toxic (T)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
GHS Precautionary statements P261-P280-P301 + P310-P311
RID/ADR UN 2811 6.1/PG 3
Risk Statements 23/24/25
RTECS YV8320000
Safety Statements 36/37-45
Hazard Class 6.1
UN Number 2811
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Packaging
1 g in glass bottle
Biochem/physiol Actions
α1-adrenoceptor antagonist; L-type calcium channel blocker. Blocks L-type Ca2+ channels in smooth and cardiac muscle, induces apoptosis of human primary and metastatic colon adenocarcinoma cells in vitro. Drug resistance reversal agent acting on Pgp, e.g. decrease renal tubule elimination of digoxin. Increases basal ATPase activity of Pgp. Substrate of Cyp3A4 and CYP2C6.
Description (简体中文)
包装
1 g in glass bottle
Biochem/physiol Actions
α1-adrenoceptor antagonist; L-type calcium channel blocker. Blocks L-type Ca2+ channels in smooth and cardiac muscle, induces apoptosis of human primary and metastatic colon adenocarcinoma cells in vitro. Drug resistance reversal agent acting on Pgp, e.g. decrease renal tubule elimination of digoxin. Increases basal ATPase activity of Pgp. Substrate of Cyp3A4 and CYP2C6.

REFERENCES