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Sigma-Aldrich

DL-α-Glycerol phosphate magnesium salt hydrate

~85% (KT)

Synonym(s):

rac-Glycero-3-phosphate magnesium salt, Magnesium glycerophosphate

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About This Item

Empirical Formula (Hill Notation):
C3H7MgO6P · xH2O
CAS Number:
927-20-8
Molecular Weight:
194.36 (anhydrous basis)
EC Number:
213-149-3
MDL number:
MFCD00153014
UNSPSC Code:
12352211
PubChem Substance ID:
57647615
NACRES:
NA.25

biological source

synthetic

Assay

~85% (KT)

form

powder

functional group

hydroxyl

lipid type

phosphoglycerides

storage temp.

room temp

SMILES string

O.[Mg++].OCC(O)COP([O-])([O-])=O

InChI

1S/C3H9O6P.Mg.H2O/c4-1-3(5)2-9-10(6,7)8;;/h3-5H,1-2H2,(H2,6,7,8);;1H2/q;+2;/p-2

InChI key

GLZHYLKPDLVZKJ-UHFFFAOYSA-L

Related Categories

General description

DL-α-Glycerol phosphate is a racemic mixture of the D- and L-glycerophosphate enantiomers.

Application

DL-α-Glycerol phosphate magnesium salt hydrate has been used:
  • in oxidase and dehydrogenase assays
  • as a component of the osteoblast differentiation medium
  • for mineralization of poly(vinyl alcohol) (PVA) hydrogels containing alkaline phosphatase designed for osteochondral regeneration


DL-a-Glycerol phosphate may be used to assess the lysogenic-strain features of agalactiae bacteriophages

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Inhibition of Escherichia coli respiratory enzymes by short visible femtosecond laser irradiation
Lu CH, et al.
Journal of Physics D: Applied Physics, 47(31), 315402-315402 (2014)
Composites of polyvinyl alcohol (PVA) hydrogel and calcium and magnesium phosphate formed by enzymatic functionalization
Douglas T EL, et al.
Materials Letters, 137, 62-67 (2014)
Jiangwei Yao et al.
Biochimica et biophysica acta, 1831(3), 495-502 (2012-09-18)
Membrane phospholipid synthesis is a vital facet of bacterial physiology. Although the spectrum of phospholipid headgroup structures produced by bacteria is large, the key precursor to all of these molecules is phosphatidic acid (PtdOH). Glycerol-3-phosphate derived from the glycolysis via
Luana Lopes Souza et al.
The Journal of endocrinology, 211(1), 65-72 (2011-07-15)
n-3 polyunsaturated fatty acids (n-3 PUFA) from fish oil (FO) exert important lipid-lowering effects, an effect also ascribed to thyroid hormones (TH) and TH receptor β1 (TRβ1)-specific agonists. n-3 PUFA effects are mediated by nuclear receptors, such as peroxisome proliferator-activated
Heinrich Topp et al.
Pharmacology, 88(3-4), 193-200 (2011-10-12)
The primary aim of the present investigation was to determine and compare the pharmacokinetic (PK) profiles of inorganic phosphate in serum and urine after intravenous administration of sodium glycerophosphate and inorganic sodium phosphate. Additionally, study product safety profiles were evaluated.
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