MilliporeSigma
All Photos(3)

G7018

Sigma-Aldrich

α-D-Glucose 1-phosphate disodium salt hydrate

≥98%, BioXtra, lyophilized powder

Synonym(s):
α-D-Glucopyranose 1-phosphate, Cori ester
Linear Formula:
C6H11O9PNa2 · xH2O
CAS Number:
Molecular Weight:
304.10 (anhydrous basis)
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.25

biological source

synthetic

Quality Level

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

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

Looking for similar products? Visit Product Comparison Guide

General description

α-D-Glucose 1-phosphate is converted into D-glucose-6-phosphate by the enzyme phosphoglucomutase.

Packaging

10 mg in glass bottle
1, 5 g in poly bottle

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.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificate of Analysis

Enter Lot Number to search for Certificate of Analysis (COA).

Certificate of Origin

Enter Lot Number to search for Certificate of Origin (COO).

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service