17766
DL-α-Glycerol phosphate magnesium salt hydrate
~85% (KT)
Sinónimos:
rac-Glycero-3-phosphate magnesium salt, Magnesium glycerophosphate
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About This Item
Fórmula empírica (notación de Hill):
C3H7MgO6P · xH2O
Número de CAS:
Peso molecular:
194.36 (anhydrous basis)
Número CE:
Número MDL:
Código UNSPSC:
12352211
ID de la sustancia en PubChem:
NACRES:
NA.25
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Productos recomendados
origen biológico
synthetic
Nivel de calidad
Ensayo
~85% (KT)
Formulario
powder
grupo funcional
hydroxyl
tipo de lípido
phosphoglycerides
temp. de almacenamiento
room temp
cadena SMILES
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
Clave InChI
GLZHYLKPDLVZKJ-UHFFFAOYSA-L
Descripción general
DL-α-Glycerol phosphate is a racemic mixture of the D- and L-glycerophosphate enantiomers.
Aplicación
DL-α-Glycerol phosphate magnesium salt hydrate has been used:
DL-a-Glycerol phosphate may be used to assess the lysogenic-strain features of agalactiae bacteriophages
- in oxidase and dehydrogenase assays[1]
- as a component of the osteoblast differentiation medium[2]
- for mineralization of poly(vinyl alcohol) (PVA) hydrogels containing alkaline phosphatase designed for osteochondral regeneration[3]
DL-a-Glycerol phosphate may be used to assess the lysogenic-strain features of agalactiae bacteriophages
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
Eyeshields, Gloves, type N95 (US)
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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)
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
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Bioanalysis, 4(10), 1175-1183 (2012-06-02)
Urinary metabolomic profiles have recently drawn a lot of attention owing to a debate regarding their possible role as potential clinical markers for prostate cancer. In this study, levels of proline, kynurenine, uracil and glycerol-3-phosphate in 126 patients with genitourinary
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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