G9753

α-D-Glucosamine 1-phosphate

• Synonym(s): 2-Amino-2-deoxy-α-D-glucopyranosyl phosphate
• Empirical Formula (Hill Notation): C₆H₁₄NO₈P
• CAS Number: 2152-75-2
• Molecular Weight: 259.15
• NACRES: NA.25
• PubChem Substance ID: 24895380
• UNSPSC Code: 12352201
• MDL number: MFCD00070181

Properties

• biological source: natural (inorganic)
• Quality Segment: 300
• assay: ≥97% (TLC)
• form: powder
• impurities: <8.5% water (Karl Fischer)
• color: white
• solubility: water: 100 mg/mL, clear, colorless
• storage temp.: −20°C
• SMILES string: NC1C(O)C(O)C(CO)OC1OP(O)(O)=O
• InChI: 1S/C6H14NO8P/c7-3-5(10)4(9)2(1-8)14-6(3)15-16(11,12)13/h2-6,8-10H,1,7H2,(H2,11,12,13)
• InChI key: YMJBYRVFGYXULK-UHFFFAOYSA-N

Description

Application

• Cellodextrin phosphorylase from Ruminiclostridium thermocellum: X-ray crystal structure and substrate specificity analysis. This study presents the enzymatic synthesis and analysis of alpha-ᴅ-Glucosamine 1-phosphate based polysaccharides using cellodextrin phosphorylase, showcasing potential for novel biomaterial development. Field et al., 2017


• Glucose-1-phosphate uridylyltransferase from Erwinia amylovora: Activity, structure and substrate specificity. This paper explores the biochemical pathway involving alpha-ᴅ-Glucosamine 1-phosphate in the context of bacterial metabolism, providing insights into microbial biochemistry and potential targets for antibacterial therapy. Field et al., 2017

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Safety Information

• Storage Class: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)