ChemicalBook--->CAS DataBase List--->253685-27-7

253685-27-7

253685-27-7 Structure

253685-27-7 Structure
IdentificationBack Directory
[Name]

1,2-didecanoyl-sn-glycero-3-phosphoethanolaMine
[CAS]

253685-27-7
[Synonyms]

1,2-didecanoyl-sn-glycero-3-phosphoethanolaMine
1,2-DIDECANOYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE;10:0 PE
(2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl bis(decanoate)
Decanoic acid, 1,1'-[(1R)-1-[[[(2-aminoethoxy)hydroxyphosphinyl]oxy]methyl]-1,2-ethanediyl] ester
[Molecular Formula]

C25H50NO8P
[MDL Number]

MFCD02259265
[MOL File]

253685-27-7.mol
[Molecular Weight]

523.64
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[form ]

powder
[InChIKey]

KKOSJVWUOHEQKA-HSZRJFAPSA-N
[SMILES]

[H][C@@](COP([O-])(OCC[NH3+])=O)(OC(CCCCCCCCC)=O)COC(CCCCCCCCC)=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

Glycerophospholipids act as regulators of various enzyme activities, and can be used as biological markers to indicate pathological states.
[Definition]

ChEBI: PE(10:0/10:0) is a phosphatidylethanolamine 20:0.
[Biological Activity]

Phosphatidylethanolamine forms pure lipid structures. It maintains membrane fluidity in eukaryotic cells. Phosphatidylethanolamine plays a critical role in autophagycell division and protein folding. It acts as a precursor for the synthesis of various protein modifications. Phosphatidylethanolamine functions as an intermediate for the synthesis of glycerophospholipid classes.
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