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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:
Molecular Weight:
760.08
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
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

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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Customers Also Viewed

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
Cell biology. Gentle slam.
R Peters et al.
Science (New York, N.Y.), 282(5397), 2213-2214 (1999-01-16)
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
Mojtaba Bagheri et al.
Antimicrobial agents and chemotherapy, 53(3), 1132-1141 (2008-12-24)
Early studies of immobilized peptides mainly focused upon the relationship between structural properties and the activity of soluble and surface-tethered sequences. The intention of this study was to analyze the influence of immobilization parameters upon the activity profile of peptides.

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