Sodium((2R,3R,4S,5R)-3,4,5,6-tetrahydroxy-1-oxohexan-2-yl)sulfamate , 95% , 38899-05-7

CAS NO.：38899-05-7

Empirical Formula: C6H12NNaO8S

Molecular Weight: 281.22

MDL number: MFCD00057972

EINECS: 609-596-2

PRODUCT Properties

• storage temp.: Inert atmosphere,Store in freezer, under -20°C
• solubility: Soluble in DMSO
• InChI: InChI=1/C6H13NO8S.Na.H/c8-1-3(7-16(13,14)15)5(11)6(12)4(10)2-9;;/h1,3-7,9-12H,2H2,(H,13,14,15);;/t3-,4+,5+,6+;;/s3
• InChIKey: XWFHXUOTHFHRAS-IWNCBHIWNA-N
• SMILES: [C@@H](C=O)(NS(O)(=O)=O)[C@@H](O)[C@H](O)[C@H](O)CO.[NaH] |&1:0,8,10,12,r|
• CAS DataBase Reference: 38899-05-7(CAS DataBase Reference)

Description and Uses

N-Sulfo-glucosamine sodium salt is a synthetic, high purity carbohydrate with a custom synthesis. It is an oligosaccharide that is also a sugar and a saccharide. The methylation of it can be achieved by glycosylation or click modification. Click modification is the addition of a carbon atom to the molecule through the reaction with an electrophile, such as N-hydroxysuccinimide ester. This modification can be used to introduce fluorine atoms into the molecules, which can improve their solubility and stability. The product has shown anti-inflammatory activities in animal models, which may be due to its ability to inhibit prostaglandin synthesis.

Safety

• WGK Germany: 3
• HS Code: 29329990