F1395

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

≥98%

• Sinonimo/i: 6-Deoxy-β-L-galactose 1-phosphate
• Formula empirica (notazione di Hill): C₆H₁₁O₈P · 2C₆H₁₄N
• Peso molecolare: 442.48
• Numero MDL: MFCD22681514
• Codice UNSPSC: 12352201
• ID PubChem: 329799679
• NACRES: NA.25

Proprietà

• Livello qualitativo: 100
• Saggio: ≥98%
• Stato: powder
• tecniche: thin layer chromatography (TLC): suitable
• Solubilità: H₂O: soluble 50 mg/mL, clear, colorless
• Temperatura di conservazione: −20°C
• Stringa SMILE: 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; FQMPFZHILABVMA-PEJHDPODSA-N

Descrizione

Applicazioni

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.

Altre note

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

Informazioni sulla sicurezza

• Codice della classe di stoccaggio: 11 - Combustible Solids
• Classe di pericolosità dell'acqua (WGK): WGK 3
• Punto d’infiammabilità (°F): Not applicable
• Punto d’infiammabilità (°C): Not applicable
• Dispositivi di protezione individuale: Eyeshields, Gloves, type N95 (US)