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About This Item
Empirical Formula (Hill Notation):
C3H5Na2O7P
CAS Number:
Molecular Weight:
230.02
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3767836
biological source
synthetic (inorganic)
Quality Segment
assay
≥93% dry basis (enzymatic)
form
powder
greener alternative product characteristics
Atom Economy
Design for Energy Efficiency
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
impurities
<14% water (NMR)
color
white
solubility
H2O: 50 mg/mL, clear, colorless to faintly yellow
cation traces
Na: 18-22% (dry basis)
greener alternative category
storage temp.
−20°C
SMILES string
[Na+].[Na+].O[C@H](COP(O)([O-])=O)C([O-])=O
InChI
1S/C3H7O7P.2Na/c4-2(3(5)6)1-10-11(7,8)9;;/h2,4H,1H2,(H,5,6)(H2,7,8,9);;/q;2*+1/p-2/t2-;;/m1../s1
InChI key
RGCJWQYUZHTJBE-YBBRRFGFSA-L
Application
D-(-)-3-Phosphoglyceric acid disodium salt has been used in a study to assess the phosphorylation of glyceric acid in aqueous solution. It has also been used in a study to characterize a glutathione- and NAD-dependent arsenate reduction linked to glycolysis.
Biochem/physiol Actions
3-Phosphoglyceric acid is an intermediate in glycolysis. It also a precursor in the formation of serine.
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 2 - STOT SE 3
target_organs
Eyes,Central nervous system, Respiratory system
Storage Class
11 - Combustible Solids
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