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Empirische Formel (Hill-System):
C3H5Li2O6P
CAS-Nummer:
Molekulargewicht:
181.92
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1708891
Technischer Dienst
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Unterstützung erhaltenbiological source
bovine (casein)
Quality Segment
assay
≥93% dry basis (enzymatic)
form
powder
impurities
~0.2 mol % D-glyceraldehyde 3-phosphate
color
white
solubility
soluble 50mg plus 1ml of H2O, clear, colorless to faintly yellow
anion traces
phosphate (PO43-): ~5 mol %
cation traces
Li: 5.5-8.0% (dry basis)
storage temp.
−20°C
SMILES string
[Li+].[Li+].OCC(=O)COP([O-])([O-])=O
InChI
1S/C3H7O6P.2Li/c4-1-3(5)2-9-10(6,7)8;;/h4H,1-2H2,(H2,6,7,8);;/q;2*+1/p-2
InChI key
QWIKESRFRWLYIA-UHFFFAOYSA-L
Application
Dihydroxyacetone phosphate (DHAP) is used in fructose metabolism, triose and glycation research. It is used in studies involving the metabolism of three-carbon sugar pools and their roles in physiological and physical processes. DHAP may be used as a substrate to help identify, differentiate and characterize fructose-bisphosphate aldolase(s) (ALDOA) and triosephosphate isomerase(s). DHAP may be used to study cellular glycation stress.
Biochem/physiol Actions
A metabolic intermediate involved in many pathways, including glycolysis and the Calvin cycle.
Dihydroxyacetone phosphate (DHAP) is a metabolic intermediate involved in many pathways, including glycolysis, gluconeogenesis, glycerol metabolism, phosphatidic acid synthesis, fat metabolism, and the Calvin cycle.
Preparation Note
Enzymatically prepared.
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.
Disclaimer
Unlike the dimethyl ketal, does not require hydrolysis prior to use as a substrate.
Lagerklasse
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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