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Merck
CN

17766

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:
Molecular Weight:
194.36 (anhydrous basis)
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352211
EC Number:
213-149-3
MDL number:
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Product Name

DL-α-Glycerol phosphate magnesium salt hydrate, ~85% (KT)

InChI key

GLZHYLKPDLVZKJ-UHFFFAOYSA-L

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

SMILES string

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

biological source

synthetic

assay

~85% (KT)

form

powder

functional group

hydroxyl

lipid type

phosphoglycerides

storage temp.

room temp

Quality Level

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

General description

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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)
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)
Peter L Freddolino et al.
Journal of bacteriology, 194(2), 303-306 (2011-11-15)
We have recently identified seven mutations in commonly used stocks of the sequenced Escherichia coli strain MG1655 which do not appear in the reference sequence. The mutations are likely to cause loss of function of the glpR and crl genes
Ying Peng et al.
International journal of pharmaceutics, 441(1-2), 482-490 (2012-11-20)
Chitosan/glycerophosphate disodium (GP) thermosensitive hydrogels were prepared for the sustained delivery of venlafaxine hydrochloride (VH) and optimization of this formulation was mainly studied. Release mechanism was investigated by applying various mathematical models to the in vitro release profiles. Overall, drug
Haruo Shimada et al.
Biochemistry, 50(19), 4114-4120 (2011-04-09)
The structure of membrane lipids in Archaea is different from those of Bacteria and Eucarya in many ways including the chirality of the glycerol backbone. Until now, heterochiral membranes were believed to be unstable; thus, no cellular organism could have

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