Cystine Disodium Salt
Cystine Disodium Salt, systematically named disodium (R,R)-3,3'-dithiobis(2-aminopropanoate), is an ionic derivative of L-cystine formed by neutralizing the two carboxyl groups of L-cystine with sodium hydroxide. Its chemical properties are determined by three core structural features: the ionic carboxylate groups, the primary amino groups, and the intramolecular disulfide bond (-S-S-). These functional groups endow the compound with distinct reactivity in acid-base reactions, redox reactions, and peptide synthesis, making it widely applicable in pharmaceuticals and nutritional science.
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Cosmetic and Nutraceutical Fields of L-Alanyl-L-cystine 1. Skin Health Supplements Due to its cysteine content, it may be included in oral or topic... |
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L-Cysteine S-Sulfate Na |
Carboxylate Group (-COO^-) Reactivity of L-Cysteine S-Sulfate Na The carboxylate group is in a deprotonated state in neutral and alkaline solutions... |
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Nutritional Fortification of L-Aspartic acid monosodium salt monohydrate As a soluble derivative of L-aspartic acid (an essential building block of... |
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DL-tryptophan |
DL-tryptophan’s primary advantages lie in its cost-effectiveness for large-scale applications, suitability for animal nutrition, versatility ... |
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L-Alanyl-L-Cystine |
Key Applications of L-Alanyl-L-Cystine1. Pharmaceuticals and TherapeuticsAntioxidant and Anti-Inflammatory Agents:The thiol group of cysteine contr... |
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