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P4142

Sigma-Aldrich

1-Oleoyl-2-palmitoyl-sn-glycero-3-phosphocholine

≥98% (GC), ≥99% (TLC)

Synonym(s):

1-(cis-9-Octadecenoyl)-2-hexadecanoyl-sn-glycero-3-phosphocholine, L-α-Phosphatidylcholine, β-palmitoyl-γ-oleoyl

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About This Item

Empirical Formula (Hill Notation):
C42H82NO8P
CAS Number:
59491-62-2
Molecular Weight:
760.08
MDL number:
MFCD00063534
UNSPSC Code:
12352211
PubChem Substance ID:
24898505
NACRES:
NA.25

biological source

synthetic (organic)

Assay

≥98% (GC)
≥99% (TLC)

form

powder

functional group

phospholipid

lipid type

phosphoglycerides

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCCCCC(=O)O[C@@H](COC(=O)CCCCCCC\C=C/CCCCCCCC)COP(O)(=O)OCC[N](C)(C)C

InChI

1S/C42H83NO8P/c1-6-8-10-12-14-16-18-20-21-23-24-26-28-30-32-34-41(44)48-38-40(39-50-52(46,47)49-37-36-43(3,4)5)51-42(45)35-33-31-29-27-25-22-19-17-15-13-11-9-7-2/h20-21,40H,6-19,22-39H2,1-5H3,(H,46,47)/b21-20-

InChI key

ZLPCRCSDGDOSCT-MRCUWXFGSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Federico Karagulian et al.
Physical chemistry chemical physics : PCCP, 10(4), 528-541 (2008-01-10)
The ozonolysis of an approximately one monolayer film of 1-oleoyl-2-palmitoyl-sn-glycero-3-phosphocholine (OPPC) on NaCl was followed in real time using diffuse reflection infrared Fourier transform spectrometry (DRIFTS) at 23 degrees C. Matrix-assisted laser desorption/ionization (MALDI) mass spectrometry and Auger electron spectroscopy
A M Jiménez-Monreal et al.
Biochemistry, 38(24), 7747-7754 (1999-07-01)
The activation of protein kinase C alpha was studied by using a lipid system consisting of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC)/1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoserine (POPS) (molar ratio 4:1) and different proportions of 1-palmitoyl-2-oleoyl-sn-glycerol (POG). The phase behavior of the lipidic system was characterized by using differential
Jeffrey F Ellena et al.
Journal of medicinal chemistry, 45(25), 5534-5542 (2002-12-03)
There is considerable interest in the use of perfluorocarbons as oxygen carriers in clinical settings; however, little is known regarding the molecular interactions made by these apolar compounds with biological membranes or their effect on membrane structure. NMR spectroscopy was
Cell biology. Gentle slam.
R Peters et al.
Science (New York, N.Y.), 282(5397), 2213-2214 (1999-01-16)
Liang Xu et al.
Journal of molecular graphics & modelling, 27(7), 829-835 (2009-02-07)
In recent years, both classification models and quantitative structure-activity relationships (QSARs) have been developed to discriminate the acute toxicity of polar narcotics and uncouplers. One of fundamental issues is how to select and interpret the molecular descriptors used in both
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