Skip to Content
Merck
All Photos(3)

Key Documents

View All Documentation

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

Sign Into View Organizational & Contract Pricing
All Photos(3)

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
Pricing and availability is not currently available.

biological source

synthetic (organic)

Quality Level

200

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000271396
0000271396
SLCG6775
SLBZ8482
SLBM1156V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

M Yoshimoto et al.
Journal of chromatography. B, Biomedical sciences and applications, 712(1-2), 59-71 (1998-08-11)
Small unilamellar vesicles (SUVs) composed of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine and 1 mol% phosphatidylethanolamine were covalently coupled to chromatographic gel beads. Interactions of liposomal lipid bilayers with several water-soluble proteins, which had been denatured or partially denatured by 0.1-5 M guanidinium hydrochloride (GuHCl)
Han-Yuan Liu et al.
ACS applied materials & interfaces, 9(41), 35526-35538 (2017-09-21)
Emerging technologies use cell plasma membrane vesicles or "blebs" as an intermediate to form molecularly complete, planar cell surface mimetics that are compatible with a variety of characterization tools and microscopy methods. This approach enables direct incorporation of membrane proteins
W Pohle et al.
Biospectroscopy, 4(4), 267-280 (1998-08-26)
An algorithm for the study of the gradual hydration of phospholipid assemblies by means of Fourier transform infrared (FTIR) spectroscopy is presented. A complete series of diacyl phosphatidylcholines (PCs) including all possible analogues with palmitoyl and oleoyl residues, namely DPPC
Kien Xuan Ngo et al.
Journal of bioscience and bioengineering, 100(5), 495-501 (2005-12-31)
The effects of heat stress and liposome treatment on the growth of Streptomyces griseus cells and chitosanase production were investigated on the basis of using the designed strategy of a stress-mediated bioprocess. The effective conditions for increasing the interaction between
C Selle et al.
Biospectroscopy, 4(4), 281-294 (1998-08-26)
The gradual hydration of phospholipid films can be effectively probed by Fourier transform infrared (FTIR) spectroscopy (cf. part I of this series). The hydration-induced changes observed for lipid IR-absorption bands are probably composed of contributions arising from the effects of
View All Related Papers

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service