L-Cysteine S-sulfate sodium salt sesquihydrate
$200.00
CAS No.: 150465-29-5
Catalog No.: 194331
Purity: 95%
MF: C6H18N2Na2O13S4
MW: 500.459
Storage: 2-8 degree Celsius
SMILES: O=C([O-])[C@@H](N)CSS(=O)(O)=O.O=C([O-])[C@@H](N)CSS(=O)(O)=O.[H]O[H].[H]O[H].[H]O[H].[Na+].[Na+]
Catalog No.: 194331
Purity: 95%
MF: C6H18N2Na2O13S4
MW: 500.459
Storage: 2-8 degree Celsius
SMILES: O=C([O-])[C@@H](N)CSS(=O)(O)=O.O=C([O-])[C@@H](N)CSS(=O)(O)=O.[H]O[H].[H]O[H].[H]O[H].[Na+].[Na+]
L-Cysteine S-sulfate sodium salt sesquihydrate; CAS No.: 150465-29-5; L-Cysteine S-sulfate sodium salt sesquihydrate. PROPERTIES: L-Cysteine S-sulfate sodium salt sesquihydrate is a crystalline solid. Its molecular formula is C3H7NNaO5S2 {1.5H2O, and the molecular weight is approximately 258.25 g/mol. The compound has a melting point of approximately 180-182 C. It is moderately soluble in water and commonly used in the form of its sodium salt. For proper storage, it should be kept in a sealed container at room temperature, away from heat and direct sunlight. As an amino acid derivative containing a sulfate group, it may exhibit certain reactivity and stability. When handling it, protective gloves and eye protection should be worn. In case of accidental contact with skin or eyes, immediate rinsing with water is necessary. APPLICATIONS: In organic synthesis, L-Cysteine S-sulfate serves as a versatile intermediate. The amino group can undergo various reactions such as acylation, alkylation, and sulfonation. The sulfate group provides opportunities for further functionalization. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For example, in the development of certain antioxidants, the structure of L-Cysteine S-sulfate can be modified to enhance its antioxidant activity and bioavailability (as reported in medicinal chemistry journals). Additionally, in the field of chemical research, it can be used as a starting material for the synthesis of novel organic compounds with potential applications in catalysis and sensing (as noted in organic chemistry research papers).
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