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132-21-8

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132-21-8 Usage

Originator

Disomer,White,US,1959

Uses

Antihistaminic.

Definition

ChEBI: The (pharmacologically active) (S)-(+)-enantiomer of brompheniramine. A histamine H1 receptor antagonist, it is used (commonly as its maleate salt) for the symptomatic relief of allergic conditions, including rhinitis nd conjunctivitis.

Manufacturing Process

The following is taken from US Patent 3,061,517. Sixteen grams of racemic 3- (2-pyridyl)-3-p-bromophenyl-N,N,-dimethylpropylamine and 9.7 grams of dphenylsuccinic acid are dissolved in 150 ml of absolute alcohol and kept at room temperature until crystallization is effected. The crystals are filtered,washed with absolute ethyl alcohol, and recrystallized from the same solvent using 5 ml there of per gram of solid. Three subsequent crystallizations from 80% alcohol give d-3-(2-pyridyl)-3-p-bromophenyl-N,N-dimethylpropylamined-phenylsuccinate; MP 152-154°C; [α]D25 91 (concentration, 1% in dimethylformamide).The free base, d-3-(2-pyridyl)-3-p-bromophenyl-N,N-dimethylpropylamine, is obtained from this salt with diethyl ether and aqueous potassium carbonate; [α]D25 +42.7 (concentration, 1% in dimethylformamide). The free base is then reacted with maleic acid.

Brand name

Disomer (Schering).

Therapeutic Function

Antihistaminic

Check Digit Verification of cas no

The CAS Registry Mumber 132-21-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 132-21:
(5*1)+(4*3)+(3*2)+(2*2)+(1*1)=28
28 % 10 = 8
So 132-21-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H19BrN2/c1-19(2)12-10-15(16-5-3-4-11-18-16)13-6-8-14(17)9-7-13/h3-9,11,15H,10,12H2,1-2H3/t15-/m0/s1

132-21-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dexbrompheniramine

1.2 Other means of identification

Product number -
Other names Brompheniramine d

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:132-21-8 SDS

132-21-8Downstream Products

132-21-8Related news

Simultaneous determination of pseudoephedrine sulfate, DEXBROMPHENIRAMINE (cas 132-21-8) maleate and loratadine in pharmaceutical preparations using derivative spectrophotometry and ratio spectra derivative spectrophotometry09/29/2019

Two new spectrophotometric methods are described for the simultaneous analysis of pseudoephedrine sulfate-dexbrompheniramine maleate (DBP) and pseudoephedrine sulfate-loratadine combinations. In the first, derivative spectrophotometry, dA/dλ values were read at zero-crossing points. In the seco...detailed

Potentialities of ITP-CZE method with diode array detection for enantiomeric purity control of DEXBROMPHENIRAMINE (cas 132-21-8) in pharmaceuticals10/01/2019

The present work illustrates potentialities of on-line combined isotachophoresis-capillary zone electrophoresis (ITP-CZE) separation techniques coupled with on-capillary diode array detector (DAD) for enantiomeric purity testing of drugs in pharmaceuticals. The general advantages of the proposed...detailed

132-21-8Relevant articles and documents

New Synthetic Route to Pheniramines via Hydroformylation of Functionalized Olefins

Botteghi, Carlo,Chelucci, Giorgio,Ponte, Gino Del,Marchetti, Mauro,Paganelli, Stefano

, p. 7125 - 7127 (2007/10/02)

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