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About This Item
Empirical Formula (Hill Notation):
C6H13O9P
CAS Number:
Molecular Weight:
260.14
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25
biological source
synthetic (inorganic)
Quality Level
Assay
≥99% (TLC)
form
liquid
concentration
~1 M in H2O (approx. 260 mg per ml)
technique(s)
thin layer chromatography (TLC): suitable
color
colorless
shipped in
dry ice
storage temp.
−20°C
SMILES string
OC(COP(O)(O)=O)C(O)C(O)C(O)C=O
InChI
1S/C6H13O9P/c7-1-3(8)5(10)6(11)4(9)2-15-16(12,13)14/h1,3-6,8-11H,2H2,(H2,12,13,14)
InChI key
VFRROHXSMXFLSN-UHFFFAOYSA-N
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Application
- Phosphonate and α-fluorophosphonate analogs of d-glucose 6-phosphate as active-site probes of 1l-myo-inositol 1-phosphate synthase.: This study explores phosphonate and α-fluorophosphonate analogs of d-glucose 6-phosphate, offering insights into their use as probes for understanding enzyme mechanisms, which could impact biochemical research methodologies (Ramos-Figueroa et al., 2023).
Biochem/physiol Actions
D-Glucose 6-phosphate binds and inhibits the activity of sarcoendoplasmic reticulum calcium ATPase in rat brains resulting in a decrease in the accumulation of calcium in the endoplasmic reticulum.
Other Notes
Prepared from G 7879.
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
涉药品监管产品
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