ChemicalBook--->CAS DataBase List--->91742-11-9

91742-11-9

91742-11-9 Structure

91742-11-9 Structure
IdentificationBack Directory
[Name]

1,2-DILIGNOCEROYL-SN-GLYCERO-3-PHOSPHOCHOLINE
[CAS]

91742-11-9
[Synonyms]

24:0 PC
1,2-dilignoceroyl-3-sn-phosphatidylcholine
1,2-DILIGNOCEROYL-SN-GLYCERO-3-PHOSPHOCHOLINE
1,2-DITETRACOSANOYL-SN-GLYCERO-3-PHOSPHOCHOLINE
1,2-DILIGNOCEROYL-SN-GLYCERO-3-PHOSPHOCHOLINE;24:0 PC
[Molecular Formula]

C56H112NO8P
[MDL Number]

MFCD00674312
[MOL File]

91742-11-9.mol
[Molecular Weight]

958.48
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
Safety DataBack Directory
[Symbol(GHS) ]


GHS06,GHS08
[Signal word ]

Danger
[Hazard statements ]

H302-H315-H319-H331-H336-H351-H361d-H372-H412
[Precautionary statements ]

P201-P273-P301+P312+P330-P302+P352-P304+P340+P311-P308+P313
Hazard InformationBack Directory
[Uses]

24:0 PC (1,2-dilignoceroyl-sn-glycero-3-phosphocholine) may be used:
  • in both short-chain micelles and longer-chain oriented multilayers and in Langmuir monolayers for structural studies of the human immunodeficiency virus 1 (HIV-1) accessory protein
  • to compare cohesion/to study the effects of lipid cohesion on the thermally induced revaporization and dissolution of microbubble condensed droplets (MCDs)
  • to study its effects on non-amyloidogenic processing of amyloid precursor protein (APP) and to study the effects of the its carbon chain length on α-secretase activity

[Uses]

24:0 PC (1,2-dilignoceroyl-sn-glycero-3-phosphocholine) may be used:
  • in short-chain micelles, longer-chain oriented multilayers and in Langmuir monolayers for structural studies
  • as an acyl chain lipid in microbubble condensed droplets (MCDs) and characterization studies
  • in phosphatidylcholine bilayer preparation for Raman spectroscopy studies

[General Description]

24:0 PC (1,2-dilignoceroyl-sn-glycero-3-phosphocholine) is a long-chain diacyl phospholipid. It consists of C24 saturated hydrocarbon chains.
[Biochem/physiol Actions]

Phosphatidylcholines (PCs) serve as a major source for eicosanoids.
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