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Merck

G6376

Sigma-Aldrich

β-Glycerophosphate disodium salt hydrate

≤2.4 mol % α-isomer(based on C3H7O6PNa2 With x H2O)

Sinónimos:

BGP, Glycerol 2-phosphate disodium salt hydrate

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About This Item

Fórmula lineal:
(HOCH2)2CHOP(O)(ONa)2 · xH2O
Número de CAS:
Peso molecular:
216.04 (anhydrous basis)
Número CE:
Número MDL:
Código UNSPSC:
12352201
ID de la sustancia en PubChem:

origen biológico

synthetic

formulario

powder

impurezas

≤2.4 mol % α-isomer (based on C3H7O6PNa2 With x H2O)

mp

102-104 °C (lit.)

solubilidad

water: 100 mg/mL, clear, colorless to very faintly yellow

cadena SMILES

O.[Na+].[Na+].OCC(CO)OP([O-])([O-])=O

InChI

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

Clave InChI

ROPZSVKNEIIIDE-UHFFFAOYSA-L

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Aplicación

β-Glycerophosphate is a classical serine-threonine phosphatase inhibitor used in kinase reaction buffers. BGP is often used in combination with other phosphatase/protease inhibitors for broad spectrum inhibition. It functions as an organic phosphate donor and has been used in culture media for mesenchymal stem cell differentiation to osteoblast-type cells. BGP is also used to buffer M17 media for Lactococcus culture in recombinant protein expression.
Initiates differentiation of bone-marrow-derived stem cells embedded in a natural collagen/chitosan gel designed for tissue engineering.

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Referencia del producto
Descripción
Precios

Pictogramas

Exclamation mark

Palabra de señalización

Warning

Frases de peligro

Clasificaciones de peligro

Eye Irrit. 2

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)


Certificados de análisis (COA)

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