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980-71-2

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980-71-2 Usage

Description

Brompheniramine is a first generation antihistamine of the propylamine class. It antagonizes histamine H1 receptors (Ki = 6.06 nM) and also inhibits the reuptake of serotonin and norepinephrine.

Chemical Properties

White Solid

Originator

Dimetane,Robins,US,1957

Uses

Different sources of media describe the Uses of 980-71-2 differently. You can refer to the following data:
1. This drug is only available in combination with other medications: Bromfed, Dimetane, Dimetapp, Drixomed, Histatab, Nasahist. The only difference between this agent and chlorpheniramine is the substitution of a bromine for a chlorine atom in brompheniramine.
2. An antihistamine and also an inhibitor of serotonin reuptake

Definition

ChEBI: The maleic acid salt of brompheniramine. A histamine H1 receptor antagonist, it is used for the symptomatic relief of allergic conditions, including rhinitis and conjunctivitis.

Manufacturing Process

Initially, 4-bromobenzyl-cyanide is reacted with sodium amide and 2- chloropyridine to give bromophenyl-pyridyl acetonitrile. This is then reacted with sodium amide then dimethyl amino ethyl chloride to give 4-bromophenyldimethylaminoethyl- pyridyl acetonitrile. This intermediate is then hydrolyzed and decarboxylated to bromphenirame using 80% H2SO4 at 140°-150°C for 24 hours. The brompheniramine maleate may be made by reaction with maleic acid in ethanol followed by recrystallization from pentanol.

General Description

Brompheniraminemaleate, (+)2-[p-bromo-α-[2-(dimethylamino)ethyl]benzyl]pyridine bimaleate (Dimetane), differs fromchlorpheniramine by the substitution of a bromine atom forthe chlorine atom. Its actions and uses are like those of chlorpheniramine.It has a half-life of 25 hours, which is almosttwice that of chlorpheniramine.

Side effects

The side effects of this medication are similar to other classes of sedative antihistamines. Some medications include parabens. Patients sensitive to parabens may develop a sensitivity reaction.

Check Digit Verification of cas no

The CAS Registry Mumber 980-71-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,8 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 980-71:
(5*9)+(4*8)+(3*0)+(2*7)+(1*1)=92
92 % 10 = 2
So 980-71-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H19BrN2.C4H4O4/c1-19(2)12-10-15(16-5-3-4-11-18-16)13-6-8-14(17)9-7-13;5-3(6)1-2-4(7)8/h3-9,11,15H,10,12H2,1-2H3;1-2H,(H,5,6)(H,7,8)/b;2-1-

980-71-2 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • TCI America

  • (B5167)  Bromopheniramine Maleate  >98.0%(HPLC)(T)

  • 980-71-2

  • 25g

  • 690.00CNY

  • Detail
  • Sigma-Aldrich

  • (B1153000)  (±)-Brompheniramine maleate salt  

  • 980-71-2

  • B1153000

  • 1,880.19CNY

  • Detail
  • USP

  • (1078008)  Brompheniramine maleate  United States Pharmacopeia (USP) Reference Standard

  • 980-71-2

  • 1078008-125MG

  • 3,691.35CNY

  • Detail

980-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name brompheniramine maleate

1.2 Other means of identification

Product number -
Other names brompheniramine (maleate)

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:980-71-2 SDS

980-71-2Synthetic route

RS-brompheniramine maleate
980-71-2

RS-brompheniramine maleate

A

S-brompheniramine maleate

S-brompheniramine maleate

B

(R)-brompheniramine maleate

(R)-brompheniramine maleate

Conditions
ConditionsYield
With sodium dihydrogenphosphate; phosphoric acid In methanol; water pH=2.75; Reagent/catalyst; Ionic liquid; Resolution of racemate;
With β‐cyclodextrin In aq. phosphate buffer pH=2.5; Resolution of racemate;

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