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About This Item
Linear Formula:
C6H11O9PNa2 · xH2O
CAS Number:
Molecular Weight:
304.10 (anhydrous basis)
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352201
EC Number:
260-154-1
MDL number:
biological source
synthetic
product line
BioXtra
assay
≥98%
form
lyophilized powder
impurities
glucose, starch, and ethanol, essentially free, 0.01-0.2% α-D-glucose 1,6-diphosphate
color
white
solubility
water: 50 mg/mL, clear
cation traces
Na: 13.7-17.1% (anhydrous)
storage temp.
−20°C
SMILES string
[Na+].[Na+].[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.2Na.H2O/c7-1-2-3(8)4(9)5(10)6(14-2)15-16(11,12)13;;;/h2-10H,1H2,(H2,11,12,13);;;1H2/q;2*+1;/p-2/t2-,3-,4+,5-,6-;;;/m1.../s1
InChI key
YWAUQXHOCBBYLP-FBNUBEQJSA-L
General description
α-D-Glucose 1-phosphate is converted into D-glucose-6-phosphate by the enzyme phosphoglucomutase.
Biochem/physiol Actions
α-D-Glucose 1-phosphate is the α-anomeric form of glucose which contains a phosphate group on the primary carbon. In certain strains of Corynebacteria, glucose 1-phosphate has been shown to induce the build up of starch-like inclusion bodies within the cell.
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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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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