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phenoxybenzamine

phenoxybenzamine Structure
CAS No.
59-96-1
Chemical Name:
phenoxybenzamine
Synonyms
Phenoxy;Dibenyline;Phenoxybenzamin;phenoxybenzamine USP/EP/BP;N-Benzyl-N-(2-chloroethyl)-1-phenoxypropan-2-aMine;N-(2-Chloroethyl)-N-(1-methyl-2-phenoxyethyl)benzylamine;BENZYLAMINE,N-(2-CHLOROETHYL)-N-(1-METHYL-2-PHENOXYETHYL)-;Benzenemethanamine, N-(2-chloroethyl)-N-(1-methyl-2-phenoxyethyl)-
CBNumber:
CB1933947
Molecular Formula:
C18H22ClNO
Molecular Weight:
303.83
MOL File:
59-96-1.mol
Modify Date:
2023/5/4 17:34:40

phenoxybenzamine Properties

Melting point 38-40°
Boiling point 381.5±27.0 °C(Predicted)
Density 1.0513 (rough estimate)
refractive index 1.5600 (estimate)
pka 6.58±0.50(Predicted)
color Crystals from pet ether
CAS DataBase Reference 59-96-1
EPA Substance Registry System N-(2-Chloroethyl)-N-(1-methyl-2-phenoxyethyl)benzenemethanamine (59-96-1)

SAFETY

Risk and Safety Statements

Toxicity LD50 oral in rat: 2500mg/kg

phenoxybenzamine Chemical Properties,Uses,Production

Uses

Antihypertensive.

World Health Organization (WHO)

Phenoxybenzamine, a long-acting alpha-adrenoreceptor antagonist, was introduced in 1953 and has been used in a variety of peripheral vascular disorders. In 1982 it was shown to have mutagenic activity and in 1985 it was found to be carcinogenic in the rat. Its approved use was subsequently restricted by several regulatory authorities and phenoxybenzamine is currently used to manage hypertensive episodes associated with phaeochromocytoma, as an adjunct to the short-term management of urinary retention due to neurogenic bladder, in the short-term treatment of benign prostatic hypertrophy in patients awaiting surgery, and in inoperable benign prostatic hypertrophy.

Safety Profile

Confirmed carcinogen with experimental carcinogenic and neoplastigenic data. Poison by intravenous and intracerebral routes. Moderately toxic by ingestion. Human reproductive effects by ingestion: spermatogenesis. Experimental reproductive effects. When heated to decomposition it emits very toxic fumes of Cland NOx.

Purification Methods

The free base is crystallised from pet ether, and the HCl is crystallised from EtOH/diethyl ether. [Beilstein 12 IV 2204.]

phenoxybenzamine Preparation Products And Raw materials

Global( 25)Suppliers
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Mylan Laboratories Ltd +91-4023550543 +91-4030866666 Telangana, India 150 58 Inquiry
Apicore Pharmaceuticals Pvt Ltd +91-2662267177 +91-2662267166 Gujarat, India 181 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
Laffans Petrochemicals Limited 09820085810 Mumbai, India 14 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 19892 58 Inquiry
Shaanxi Dideu Medichem Co. Ltd +86-029-89586680 +86-18192503167 China 9030 58 Inquiry
Finetech Industry Limited +86-27-87465837 +8618971612321 China 9624 58 Inquiry
Dayang Chem (Hangzhou) Co.,Ltd. 571-88938639 +8617705817739 China 52861 58 Inquiry
GIHI CHEMICALS CO.,LIMITED +8618058761490 China 49999 58 Inquiry
Finetech Industry Limited 027-87465837 19945049750 China 9618 58 Inquiry
Phenoxybenzamin Phenoxy BENZYLAMINE,N-(2-CHLOROETHYL)-N-(1-METHYL-2-PHENOXYETHYL)- Dibenyline N-(2-Chloroethyl)-N-(1-methyl-2-phenoxyethyl)benzylamine N-Benzyl-N-(2-chloroethyl)-1-phenoxypropan-2-aMine Benzenemethanamine, N-(2-chloroethyl)-N-(1-methyl-2-phenoxyethyl)- phenoxybenzamine USP/EP/BP 59-96-1 Isotopically Labeled Pharmaceutical Reference Standard