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P0537

Sigma-Aldrich

1,2-Dilinoleoyl-sn-glycero-3-phosphocholine

≥99% (TLC), lyophilized powder

Synonym(s):

(7R,18Z,21Z)-4-Hydroxy-N,N,N-trimethyl-10-oxo-7-[[(9Z,12Z)-1-oxo-9,12-octadecadien-1-yl]oxy]-3,5,9-trioxa-4-phosphaheptacosa-18,21-dien-1-aminium 4-oxide, inner salt, 1,2-Di(cis-9,12-octadecadienoyl)-sn-glycero-3-phosphocholine, 1,2-Dilinoleoyl-sn-3-glycerophosphorylcholine, 3-sn-Phosphatidylcholine, 1,2-dilinoleoyl, L-α-Dilinoleoyl phosphatidylcholine, L-Dilinoleoyllecithin, Dilinoleoyl-L-α-phosphatidylcholine, PC(18:2(9Z,12Z)/18:2(9Z,12Z))

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About This Item

Empirical Formula (Hill Notation):
C44H80NO8P
CAS Number:
998-06-1
Molecular Weight:
782.08
Beilstein/REAXYS Number:
5212188
EC Number:
213-647-0
MDL number:
MFCD00135289
UNSPSC Code:
51191904
PubChem Substance ID:
24898112
NACRES:
NA.25

biological source

synthetic (organic)

Quality Level

200

assay

≥99% (TLC)

form

lyophilized powder

functional group

amine
ester

lipid type

phosphoglycerides

shipped in

ambient

storage temp.

−20°C

SMILES string

[O-]P(OCC[N+](C)(C)C)(OC[C@]([H])(OC(CCCCCCC/C=C\C/C=C\CCCCC)=O)COC(CCCCCCC/C=C\C/C=C\CCCCC)=O)=O

InChI

1S/C44H80NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-34-36-43(46)50-40-42(41-52-54(48,49)51-39-38-45(3,4)5)53-44(47)37-35-33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h14-17,20-23,42H,6-13,18-19,24-41H2,1-5H3/b16-14-,17-15-,22-20-,23-21-/t42-/m1/s1

InChI key

FVXDQWZBHIXIEJ-LNDKUQBDSA-N

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Packaging

Packaged under Argon.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

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Lars V Schäfer et al.
Proceedings of the National Academy of Sciences of the United States of America, 108(4), 1343-1348 (2011-01-06)
Cell membranes are comprised of multicomponent lipid and protein mixtures that exhibit a complex partitioning behavior. Regions of structural and compositional heterogeneity play a major role in the sorting and self-assembly of proteins, and their clustering into higher-order oligomers. Here
Jeffery B Klauda et al.
The journal of physical chemistry. B, 114(23), 7830-7843 (2010-05-26)
A significant modification to the additive all-atom CHARMM lipid force field (FF) is developed and applied to phospholipid bilayers with both choline and ethanolamine containing head groups and with both saturated and unsaturated aliphatic chains. Motivated by the current CHARMM
Joakim P M Jämbeck et al.
The journal of physical chemistry. B, 116(10), 3164-3179 (2012-02-23)
An all-atomistic force field (FF) has been developed for fully saturated phospholipids. The parametrization has been largely based on high-level ab initio calculations in order to keep the empirical input to a minimum. Parameters for the lipid chains have been
Wei Liu et al.
Free radical biology & medicine, 50(1), 166-178 (2010-11-05)
We report herein that oxidation of a mitochondria-specific phospholipid tetralinoleoyl cardiolipin (L(4)CL) by cytochrome c and H(2)O(2) leads to the formation of 4-hydroxy-2-nonenal (4-HNE) via a novel chemical mechanism that involves cross-chain peroxyl radical addition and decomposition. As one of
Joel H Nyström et al.
Biophysical journal, 99(2), 526-533 (2010-07-21)
Cholesterol is distributed unevenly between different cellular membrane compartments, and the cholesterol content increases from the inner bilayers toward the plasma membrane. It has been suggested that this cholesterol gradient is important in the sorting of transmembrane proteins. Cholesterol has
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