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10008-75-0

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10008-75-0 Usage

General Description

(2R,3R)-2,3-disulfanylbutanedioic acid, also known as thiodicarboxylic acid, is a dicarboxylic acid containing two thiol functional groups. It is a compound with a molecular formula of C6H8O4S2. This chemical is used as a chelating agent, meaning it can form stable complexes with metal ions. It has potential applications in various fields including medicine, agriculture, and industrial processes. Additionally, it has been studied for its antioxidant properties and potential use in the treatment of various diseases. The compound's unique structure and properties make it a valuable and versatile chemical in many applications.

Check Digit Verification of cas no

The CAS Registry Mumber 10008-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,0 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10008-75:
(7*1)+(6*0)+(5*0)+(4*0)+(3*8)+(2*7)+(1*5)=50
50 % 10 = 0
So 10008-75-0 is a valid CAS Registry Number.

10008-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R)-2,3-bis(sulfanyl)butanedioic acid

1.2 Other means of identification

Product number -
Other names Succinic acid,2,3-dimercapto-,(+-)

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:10008-75-0 SDS

10008-75-0Relevant articles and documents

Comparative in vivo lead mobilization of meso- and rac-2,3-dimercaptosuccinic acids in albino Wistar rats

Jones, Mark M.,Singh, Pramod K.,Kostial, Krista,Blanusa, Maja,Piasek, Martina,Restek-Samarozija, Nada

, p. 182 - 186 (2007/10/03)

Comparison of the racemic and meso forms of 2,3-dimercaptosuccinic acid (DMSA) in lead mobilization from lead-loaded albino Wistar rats demonstrates that the racemic form is significantly more effective in reducing femur lead levels. After four oral doses at 0.5 mmol/kg, femur lead levels were reduced to 87% of control values by meso-DMSA and to 50% of control levels by rac-DMSA. Similarly, when the dose was increased to 1.0 mmol/kg, femur lead levels were reduced to 69% of control levels by meso-DMSA and to 45% of control levels by rac-DMSA. A similar pattern was found for renal lead levels. Brain lead concentrations were significantly lower in treated groups than in control groups, but no differences were found between rac- and meso-DMSA. Rac-DMSA is more soluble than meso-DMSA in acetonitrile, ethyl acetate, and ethyl ether. The partition coefficient of rac-DMSA in the n-octanol/water system was found to be about 2.8. These results indicate that rac-DMSA deserves further attention as a possible substitute for meso-DMSA.

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