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2-amino-3-sulfanylbutanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

43083-51-8

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43083-51-8 Usage

Chemical Structure

Contains a thiol group (-SH)

Odor

Pungent, distinctive odor due to the thiol group

Biological Processes

Metabolism of cysteine and methionine
Synthesis of glutathione (antioxidant)

Potential Applications

Prevention of neurodegenerative diseases
Cosmetic formulations
Pharmaceutical formulations

Physiological Role

Vital role in various physiological processes

Industrial Applications

Potential applications in medicine and industry

Check Digit Verification of cas no

The CAS Registry Mumber 43083-51-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,0,8 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 43083-51:
(7*4)+(6*3)+(5*0)+(4*8)+(3*3)+(2*5)+(1*1)=98
98 % 10 = 8
So 43083-51-8 is a valid CAS Registry Number.

43083-51-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-3-sulfanylbutanoic acid

1.2 Other means of identification

Product number -
Other names Hnv

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:43083-51-8 SDS

43083-51-8Relevant academic research and scientific papers

β-Substituted Cysteines as Sequestering Agents for Ethanol-Derived Acetaldehyde in Vivo

Nagasawa, Herbert T.,Elberling, James E.,Roberts, Jeanette C.

, p. 1373 - 1378 (2007/10/02)

A series of β-mono- and β,β-disubstituted cysteins were evaluated in rats as sequestering agents for metabolically generated acetaldehyde (AcH) during the oxidation of ethanol in vivo and compared against D-(-)-penicillamine.Both threo- (5) and erythro-β-

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