10008-75-0 Usage
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. (2R,3R)-2,3-disulfanylbutanedioic acid's unique structure and properties make it a valuable and versatile chemical in many applications.
Uses
Used in Chelating Applications:
(2R,3R)-2,3-disulfanylbutanedioic acid is used as a chelating agent for its ability to form stable complexes with metal ions. This property makes it useful in various applications, such as in the removal of heavy metals from water or soil, or in the stabilization of metal ions in industrial processes.
Used in Antioxidant Applications:
(2R,3R)-2,3-disulfanylbutanedioic acid is used as an antioxidant for its potential to protect against oxidative stress and damage. Its antioxidant properties may have applications in the prevention or treatment of various diseases, such as neurodegenerative disorders or cardiovascular diseases.
Used in Pharmaceutical Applications:
(2R,3R)-2,3-disulfanylbutanedioic acid is used as a pharmaceutical agent for its potential therapeutic effects in the treatment of various diseases. Its unique structure and properties make it a promising candidate for drug development and medicinal applications.
Used in Agricultural Applications:
(2R,3R)-2,3-disulfanylbutanedioic acid is used in agriculture for its potential applications in improving crop yield, enhancing nutrient uptake, or providing protection against pests and diseases. Its chelating properties may also be useful in the management of soil fertility and nutrient availability.
Used in Industrial Applications:
(2R,3R)-2,3-disulfanylbutanedioic acid is used in industrial processes for its potential applications in the stabilization of metal ions, the removal of heavy metals from waste streams, or the development of new materials with unique properties. Its versatility and chemical properties make it a valuable compound in various industrial 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.
10008-75-0Relevant 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.
