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经验公式(希尔记法):
C6H11K2O9P · 5H2O
化学文摘社编号:
分子量:
426.39
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
242-783-3
Beilstein/REAXYS Number:
3922740
MDL number:
biological source
bovine milk
Quality Segment
type
Type II
assay
≥98% (HPLC)
form
powder
technique(s)
HPLC: suitable
impurities
≤0.5 mol % glucose 1-phosphate.
color
white
solubility
water: 50 mg/mL, clear, colorless
cation traces
K: 20.4-26.1% (anhydrous)
storage temp.
−20°C
SMILES string
[K+].[K+].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O
InChI
1S/C6H13O9P.2K.5H2O/c7-1-2-3(8)4(9)5(10)6(14-2)15-16(11,12)13;;;;;;;/h2-10H,1H2,(H2,11,12,13);;;5*1H2/q;2*+1;;;;;/p-2/t2-,3+,4+,5-,6-;;;;;;;/m1......./s1
InChI key
ZYBRMLNCQMITLC-JFYWUTKTSA-L
Application
α-D-Galactose 1-phosphate may be used in Leloir pathway of galactose metabolism research to study the process of UDP-Galactose (UDP-Gal) formation via UDP-glucose:α-D-galactose-1-phosphate uridylyltransferase(s) (EC 2.7.7.12). It may be used to identify and characterize and study the functions of galactose-1-phosphate uridylyltransferase(s).
Biochem/physiol Actions
Metabolite intermediate in the interconversion of glucose and galactose. Also involved in galactose metabolism and nucleotide sugar metabolism
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.
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)