Dihydroxyacetone phosphate dilithium salt

SIGMA/D7137 - ≥93% dry basis (enzymatic)

Synonym: 1,3-Dihydroxy-2-propanone 1-phosphate dilithium salt; 1-Hydroxy-3-(phosphonooxy)-2-propanone dilithium salt; DHAP

CAS Number: 102783-56-2
Empirical Formula (Hill Notation): C₃H₅Li₂O₆P
Molecular Weight: 181.92
MDL Number: MFCD00077731
Linear Formula: C₃H₅Li₂O₆P
Product Type: Chemical

Catalog Number	PKG Qty.	Price


45-D7137-5MG	5 mg	$0.00 1/EA CALL FOR PRICE	Add To Favorites
45-D7137-10MG	10 mg	$0.00 1/EA CALL FOR PRICE	Add To Favorites
45-D7137-25MG	25 mg	$258.00 1/EA	Add To Favorites
45-D7137-100MG	100 mg	$0.00 1/EA CALL FOR PRICE	Add To Favorites
45-D7137-250MG	250 mg	$0.00 1/EA CALL FOR PRICE	Add To Favorites

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This image depicts SKU: D7137-100MG

Properties
Descriptions
Safety Info.
Basic Data

anion traces	phosphate (PO₄^3-): ~5 mol %
assay	≥93% dry basis (enzymatic)
biological source	bovine (casein)
cation traces	Li: 5.5-8.0% (dry basis)
color	white
form	powder
impurities	~0.2 mol % D-glyceraldehyde 3-phosphate
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
Quality Level	200
SMILES string	[Li+].[Li+].OCC(=O)COP([O-])([O-])=O
solubility	soluble 50mg plus 1ml of H2O, clear, colorless to faintly yellow
storage temp.	−20°C

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.
Biochem/physiol Actions:	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.
Disclaimer:	Unlike the dimethyl ketal, does not require hydrolysis prior to use as a substrate.
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.
Packaging:	100, 250 mg in poly bottle
Packaging:	5, 10, 25 mg in glass bottle
Preparation Note:	Enzymatically prepared.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

Purity	≥93% dry basis (enzymatic)
Storage Temp.	−20°C
UNSPSC	12352201

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