盐酸维拉帕米

Name: 盐酸维拉帕米
Brand: 济南圣和化工有限公司

CAS 23313-68-0C27H39ClN2O4MW 491.1

盐酸维拉帕米，CAS 登记号 23313-68-0，由济南圣和化工有限公司现货供应，可提供纯度按批次COA提供(不公开发布) 的规格，下游主要用于有机化学品。支持样品与小批量试用，批量价格请联系我们获取，验收以批次 COA 为准。

规格参数

CAS号23313-68-0

分子式C27H39ClN2O4

分子量491.1

纯度按批次COA提供(不公开发布)

包装按订单/批次确认(不公开发布)

应用领域有机化学品

类别有机化学品

用途与场景

有机化学品

包装与供货

包装规格按订单/批次确认(不公开发布)

纯度规格按批次COA提供(不公开发布)

储存条件密封、阴凉干燥处保存

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主要涉及有机化学品。

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PubChem 公开数据

Description

Verapamil hydrochloride · CAS 23313-68-0 · C27H39ClN2O4. UNII V3888OEY5R.

Identification

CAS Registry Number	23313-68-0
PubChem CID	62969
Molecular formula	C27H39ClN2O4
IUPAC name	2-(3,4-dimethoxyphenyl)-5-[2-(3,4-dimethoxyphenyl)ethyl-methylamino]-2-propan-2-ylpentanenitrile;hydrochloride
UNII (FDA)	V3888OEY5R

Computed Descriptors

Molecular Weight	491.1
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	13
Exact Mass	490.2598354
Monoisotopic Mass	490.2598354
Topological Polar Surface Area	64
Heavy Atom Count	34
Formal Charge	0
Complexity	606

Physical description & handling notes

208.9 Å² [M+H]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

GHS Hazard Classification

Reported hazard statements	H301, H311 (10.4%), H302 (15.6%), H315 (18.1%), H319 (18.1%), H330 (60%), H331 (16.7%), H335 (18.9%)

H301+H311 (10.4%): Toxic if swallowed or in contact with skin [Danger Acute toxicity, oral; acute toxicity, dermal]

H301 (99.6%): Toxic if swallowed [Danger Acute toxicity, oral]

Documented Uses

Drug used for the treatment of hypertension, angina, and cluster headache prophylaxis.
Agents used for the treatment or prevention of cardiac arrhythmias. They may affect the polarization-repolarization phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibers. Anti-arrhythmia agents are often classed into four main groups according to their mechanism of action: sodium channel blockade, beta-adrenergic blockade, repolarization prolongation, or calcium channel blockade.
A class of drugs that act by selective inhibition of calcium influx through cellular membranes.
Drugs used to cause dilation of the blood vessels.
Calcium Channel Blocker [EPC]; Calcium Channel Antagonists [MoA]; Cytochrome P450 3A Inhibitors [MoA]; Cytochrome P450 3A4 Inhibitors [MoA]; P-Glycoprotein Inhibitors [MoA]
Route of Elimination: Approximately 70% of an administered dose is excreted as metabolites in the urine and 16% or more in the feces within 5 days. About 3% to 4% is excreted in the urine as unchanged drug. Half Life: 2.8-7.4 hours

Synonyms

Verapamil hydrochloride; 152-11-4; Verapamil HCl; Verelan; Covera; Isoptin SR; Verelan PM; Calan SR; DTXSID2034095; NSC-272366; NSC-657799; V3888OEY5R; Verapamili hydrochloridum; NSC657799; LU-20175; (+-)-Verapamil hydrochloride

Frequently Asked Questions

What are the CAS number and molecular formula of Verapamil hydrochloride?

CAS 23313-68-0; molecular formula C27H39ClN2O4; molecular weight — g/mol.

What other names is Verapamil hydrochloride known by?

Verapamil hydrochloride, 152-11-4, Verapamil HCl, Verelan, Covera, Isoptin SR.

Is Verapamil hydrochloride classified as hazardous?

Hazard statements reported: H301, H311, H302, H315, H319.

Facts on this page are taken from PubChem (US National Library of Medicine) and Wikidata. Grade-specific data — assay, moisture, particle size, packaging, shelf life — is issued per batch on the COA and is not published here.

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