F1395

β-L-Fucose 1-phosphate bis(cyclohexylammonium) salt

≥98%

• Synonym(s): 6-Deoxy-β-L-galactose 1-phosphate
• Empirical Formula (Hill Notation): C₆H₁₁O₈P · 2C₆H₁₄N
• Molecular Weight: 442.48
• NACRES: NA.25
• PubChem Substance ID: 329799679
• UNSPSC Code: 12352201
• MDL number: MFCD22681514

Properties

• Quality Segment: 100
• assay: ≥98%
• form: powder
• technique(s): thin layer chromatography (TLC): suitable
• solubility: H₂O: soluble 50 mg/mL, clear, colorless
• storage temp.: −20°C
• SMILES string: NC1CCCCC1.NC2CCCCC2.C[C@@H]3O[C@H](OP(O)(O)=O)[C@@H](O)[C@H](O)[C@@H]3O
• InChI: 1S/2C6H13N.C6H13O8P/c2*7-6-4-2-1-3-5-6;1-2-3(7)4(8)5(9)6(13-2)14-15(10,11)12/h2*6H,1-5,7H2;2-9H,1H3,(H2,10,11,12)/t;;2-,3+,4+,5-,6+/m..0/s1
• InChI key: FQMPFZHILABVMA-PEJHDPODSA-N

Description

Application

β-L-Fucose 1-phosphate is suitable as both substrate and product to identify, differentiate and characterize GTP fucose pyrophosphorylase(s) (GFPP; fucose-1-phosphate guanylyltransferases) involved in the formation of the nucleotide-sugar GDP-beta-l-fucose and other fucosylation donor substrates such as 3,3′-Diaminobenzidine (GDP)-β-l-fucose. β-L-Fucose 1-phosphate may be used to generate new fucosylation donor substrates for use in glycan fucosylation research.[1][2]

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)