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Etilefrin Hydrochloride is a crystalline solid that belongs to the class of Sympathomimetic amines. It is characterized by its vasoconstrictor properties and functions as a potent stimulant of the sympathetic nervous system.

534-87-2

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534-87-2 Usage

Uses

Used in Pharmaceutical Industry:
Etilefrin Hydrochloride is used as an antihypotensive agent for the treatment of low blood pressure. It helps to increase blood pressure by constricting blood vessels and stimulating the heart, which improves blood flow and overall circulation.
Used in Medical Applications:
Etilefrin Hydrochloride is used as a vasoconstrictor in various medical procedures. Its sympathomimetic properties make it effective in constricting blood vessels, which can be beneficial during surgeries or in situations where controlling blood loss is crucial.
Used in Emergency Medicine:
In emergency medicine, Etilefrin Hydrochloride is used as a vasoconstrictor to manage conditions like hypotension and shock. Its rapid action in increasing blood pressure makes it a valuable tool in stabilizing critically ill patients.

Check Digit Verification of cas no

The CAS Registry Mumber 534-87-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 534-87:
(5*5)+(4*3)+(3*4)+(2*8)+(1*7)=72
72 % 10 = 2
So 534-87-2 is a valid CAS Registry Number.

534-87-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl-[2-hydroxy-2-(3-hydroxyphenyl)ethyl]azanium,chloride

1.2 Other means of identification

Product number -
Other names etilefrine hydrochloride

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:534-87-2 SDS

534-87-2Relevant academic research and scientific papers

Asymmetrical synthesis of (R)(-)- and (S)(+)- etilefrine by enantioselective hydrogenation and the effects of enantiomers in an animal experiment

Knorr,Reichl,Traunecker,Knappen,Brandt

, p. 1709 - 1713 (2007/10/02)

The enantiomers of etilefrine Effortil were produced by enantioselective hydrogenation. The optical purity was determined by conversion with (+)-[(R)-tetrahydrofurfuryl-(1S)-camphor-10-sulfonate] to N-[R)-tetrahydrofurfuryl]-etilefrine and subsequent sepa

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