49225
α-D-Glucose 1,6-bisphosphate potassium salt hydrate
≥99.0% (TLC)
Synonym(s):
α-D-Glucose 1,6-diphosphate potassium salt hydrate
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About This Item
Empirical Formula (Hill Notation):
C6H10K4O12P2 · xH2O
CAS Number:
Molecular Weight:
492.48 (anhydrous basis)
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352201
MDL number:
Quality Segment
assay
≥99.0% (TLC)
form
solid
impurities
≤15% water
color
white
solubility
H2O: 50 mg/mL, clear, colorless
storage temp.
−20°C
SMILES string
[K+].[K+].[K+].[K+].O[C@H]1[C@H](O)[C@@H](COP([O-])([O-])=O)O[C@H](OP([O-])([O-])=O)[C@@H]1O
InChI
1S/C6H14O12P2.4K/c7-3-2(1-16-19(10,11)12)17-6(5(9)4(3)8)18-20(13,14)15;;;;/h2-9H,1H2,(H2,10,11,12)(H2,13,14,15);;;;/q;4*+1/p-4/t2-,3-,4+,5-,6-;;;;/m1..../s1
InChI key
OVRXVCAVDXBPQT-QMKHLHGBSA-J
Application
α-D-Glucose 1,6-bisphosphate is used in the identification, differentiation and characterization of α-phosphoglucomutase(s), β-phosphoglucomutase(s) and α- and β-hexoglucomutase(s).
Biochem/physiol Actions
Metabolite formed via the activity of Glucose-1,6-biphosphate synthase. Glucose-1,6-biphosphate (G-1,6-BP) acts as an inhibitor of hexokinase function and an activator of phosphofructokinase-1 and pyruvate kinase. G-1,6-BP also acts as a coenzyme for phosphoglucomutate and a cofactor for phosphopentomutase.
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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