1,3,4,6-Tetra-O-acetyl-2-amino-2-deoxy-β-D-glucopyranose Hydrochloride

• CAT Number: R001979
• CAS Number: 10034-20-5
• Molecular Formula: C₁₄H₂₂ClNO₉
• Molecular Weight: 383.78
• Purity: ≥95%
• Synonyms: 2-Amino-2-deoxy-β-D-glucopyranose 1,3,4,6-Tetraacetate Hydrochloride; NSC 82044
• Storage: -20°C
• IUPAC Name: [(2R,3S,4R,5R,6S)-3,4,6-triacetyloxy-5-aminooxan-2-yl]methyl acetate;hydrochloride
• InChI: InChI=1S/C14H21NO9.ClH/c1-6(16)20-5-10-12(21-7(2)17)13(22-8(3)18)11(15)14(24-10)23-9(4)19;/h10-14H,5,15H2,1-4H3;1H/t10-,11-,12-,13-,14-;/m1./s1
• InChIKey: BQLUYAHMYOLHBX-XAWYEFCRSA-N
• SMILES: CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)OC(=O)C)N)OC(=O)C)OC(=O)C.Cl

1,3,4,6-Tetra-O-acetyl-2-amino-2-deoxy-β-D-glucopyranose Hydrochloride(CAT: R001979) is an acetylated glucosamine derivative commonly used as a key intermediate in the synthesis of glycosides, oligosaccharides, and glycopeptides. The acetyl protection enhances solubility in organic solvents and allows for selective deprotection and functionalization at the anomeric or amine positions. Its β-configuration and amino functionality make it ideal for constructing N-linked glycoconjugates in carbohydrate chemistry and drug development. This hydrochloride salt form improves stability and handling during storage. Widely applied in glycosylation reactions and structural carbohydrate studies, it is essential for researchers working in medicinal chemistry, glycobiology, and synthetic carbohydrate research.