CAS 10255-67-1
:Propanoic acid, 3-mercapto-2-oxo-, sodium salt (1:1)
Description:
Propanoic acid, 3-mercapto-2-oxo-, sodium salt (1:1), also known by its CAS number 10255-67-1, is a sodium salt derivative of a mercapto acid. This compound features a propanoic acid backbone with a mercapto group (-SH) and a keto group (C=O) at specific positions, contributing to its unique reactivity and properties. It is typically characterized by its solubility in water due to the ionic nature of the sodium salt, which enhances its bioavailability and potential applications in various fields. The presence of the mercapto group imparts thiol characteristics, making it a potential reducing agent and a participant in various biochemical reactions. This compound may exhibit antimicrobial properties and could be utilized in pharmaceutical formulations or as a biochemical reagent. Its stability, reactivity, and solubility make it of interest in both research and industrial applications, particularly in organic synthesis and biochemistry. As with all chemical substances, proper handling and safety measures should be observed due to its reactive functional groups.
Formula:C3H4O3S·Na
InChI:InChI=1S/C3H4O3S.Na/c4-2(1-7)3(5)6;/h7H,1H2,(H,5,6);
InChI key:InChIKey=UYCJRWVMGQXHEW-UHFFFAOYSA-N
SMILES:C(C(O)=O)(CS)=O.[Na]
Synonyms:- 2-Oxo-3-Sulfanylpropanoic Acid
- 3-Mercapto-2-oxopropionic acid sodium salt
- Mercaptopyruvic acid, sodium salt
- Propanoic acid, 3-mercapto-2-oxo-, monosodium salt
- Propanoic acid, 3-mercapto-2-oxo-, sodium salt (1:1)
- Pyruvic acid, mercapto-, sodium salt
- Sodium 2-Oxo-3-Sulfanylpropanoate
- Sodium 3-mercaptopyruvate
- Sodium mercaptopyruvate
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Found 4 products.
sodium 2-oxo-3-sulfanylpropanoate
CAS:Formula:C3H3NaO3SPurity:95%Color and Shape:SolidMolecular weight:142.1089Sodium 3-Mercapto-2-Oxopropanoate
CAS:<p>Sodium 3-Mercapto-2-Oxopropanoate</p>Purity:95%Molecular weight:142.11g/molSodium mercaptopyruvate
CAS:<p>Sodium mercaptopyruvate is a pyruvate compound that is synthesized by the reaction of sodium sulfide with 3-bromopyruvic acid. It has been shown to be effective in treating emphysema, chronic bronchitis and seborrheic dermatitis. Sodium mercaptopyruvate has also been found to modify the activity of enzymes that are related to inflammation and autoimmune diseases. This drug is an efficient nucleophile, which is important for its ability to interact with proteins via covalent modification. The compound can also be used as a substrate for various dehydrogenases, which can lead to metabolic reactions mediated by these enzymes.</p>Formula:C3H3NaO3SPurity:Min. 95%Color and Shape:SolidMolecular weight:142.11 g/mol



