1,2-DILINOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE Chemical Properties

storage temp. 

-20°C

solubility 

Ethanol: 25 mg/ml

form 

lyophilized powder

color 

White to off-white

biological source

synthetic (organic)

BRN 

5212188

InChIKey

FVXDQWZBHIXIEJ-UUPASWAYNA-N

SMILES

[C@H](OC(=O)CCCCCCC/C=C\C/C=C\CCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)COC(=O)CCCCCCC/C=C\C/C=C\CCCCC |&1:0,r|

Safety Information

WGK Germany 

1

F 

1-8-10

HS Code 

2923200000

MSDS

• Language:English Provider:SigmaAldrich

1,2-DILINOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE Usage And Synthesis

Uses

18:2 (Cis) PC (DLPC) has been used for liposome preparation.

Definition

ChEBI: A 1,2-diacyl-sn-glycero-3-phosphocholine in which the acyl groups at positions 1 and 2 are specified as linoleoyl [(9Z,12Z)-octadeca-9,12-dienoyl].

General Description

18:2 (Cis) PC (DLPC) is a synthetic phosphatidylcholine.

References

[1] MARKUS RITTER. Evidence for the formation of symmetric and asymmetric DLPC-DAPC lipid bilayer domains.[J]. Cellular Physiology and Biochemistry, 2013, 32 1: 46-52. DOI: 10.1159/000350122
[2] AZZEDINE MAZARI  Ryo Y  Satoshi Iwamoto. Effects of linoleic acid position in phosphatidylcholines and cholesterol addition on their rates of peroxidation in unilamellar liposomes.[J]. Bioscience, Biotechnology, and Biochemistry, 2010, 74 5: 1013-1017. DOI: 10.1271/bbb.90896
[3] L A BAGATOLLI  E G. A correlation between lipid domain shape and binary phospholipid mixture composition in free standing bilayers: A two-photon fluorescence microscopy study.[J]. Biophysical journal, 2000, 79 1: 434-447. DOI: 10.1016/s0006-3495(00)76305-3

1,2-DILINOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE(998-06-1)Related Product Information

• 2-LINOLEOYL-RAC-GLYCEROL
• DILINOLEIC ACID
• 1-LINOLEOYL-2-HYDROXY-SN-GLYCERO-3-PHOSPHORYLCHOLINE
• Linolenic acid
• ISOPROPYL LINOLEATE
• METHYL LINOLEATE
• 1,2-DILINOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE
• ETHYL LINOLEATE
• LINOLEIC ACID PROPYL ESTER
• METHYL LINOLENATE