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850465C

Avanti

18:0-16:0 PC

1-stearoyl-2-palmitoyl-sn-glycero-3-phosphocholine, chloroform

Synonym(s):

1-octadecanoyl-2-hexadecanoyl-sn-glycero-3-phosphocholine; SPPC; PC(18:0/16:0)

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About This Item

Empirical Formula (Hill Notation):
C42H84NO8P
CAS Number:
59403-53-1
Molecular Weight:
762.09
UNSPSC Code:
12352211

assay

>99% (TLC)

form

liquid

packaging

pkg of 1 × 2.5 mL (850465C-25mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 850465C

concentration

10 mg/mL (850465C-25mg)

lipid type

phospholipids
cardiolipins

shipped in

dry ice

storage temp.

−20°C

General description

Phosphatidylcholines (PCs) are amphipathic molecules, which accounts for approximately 40−50% of the total cellular phospholipids. 18:0-16:0 PC (1-stearoyl-2-palmitoyl-sn-glycero-3-phosphocholine) is an asymmetric lipid.

Application

18:0-16:0 PC (1-stearoyl-2-palmitoyl-sn-glycero-3-phosphocholine) may be used:
  • in bilayer membranes to study the thermodynamic properties of phase transitions
  • as a carrier in unilamellar vesicles to evaluate the fragmentation of hydroperoxy endoperoxide 13-HP-Endo-PC in a model membrane
  • as a lipid standard in liquid chromatography−mass spectrometry analysis

Biochem/physiol Actions

Phosphatidylcholine (PC) has the ability to block the penetrance of bacteria by acting as a surfactant.

Packaging

5 mL Clear Glass Sealed Ampule (850465C-25mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

target_organs

Central nervous system

Storage Class

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk_germany

WGK 3

flash_point_f

does not flash

flash_point_c

does not flash

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Inflammatory Bowel Disease
Parian AM, et al.
Integrative Medicine, 501-516 (2018)
Xiaodong Gu et al.
Chemical research in toxicology, 24(7), 1080-1093 (2011-05-17)
Biologically active phospholipids that incorporate an oxidatively truncated acyl chain terminated by a γ-hydroxyalkenal are generated in vivo. The γ-hydroxyalkenal moiety protrudes from lipid bilayers like whiskers that serve as ligands for the scavenger receptor CD36, fostering endocytosis, e.g., of
Masaki Goto et al.
Biochimica et biophysica acta, 1778(4), 1067-1078 (2008-01-15)
The bilayer phase transitions of palmitoylstearoyl-phosphatidylcholine (PSPC), diheptadecanoyl-PC (C17PC) and stearoylpalmitoyl-PC (SPPC) which have the same total carbon numbers in the two acyl chains were observed by differential scanning calorimetry and high-pressure optical method. As the temperature increased, these bilayers
Jelske N van der Veen et al.
Biochimica et biophysica acta. Biomembranes, 1859(9 Pt B), 1558-1572 (2017-04-16)
Phosphatidylcholine (PC) and phosphatidylethanolamine (PE) are the most abundant phospholipids in all mammalian cell membranes. In the 1950s, Eugene Kennedy and co-workers performed groundbreaking research that established the general outline of many of the pathways of phospholipid biosynthesis. In recent
Simon Becher et al.
Analytical chemistry, 90(19), 11486-11494 (2018-09-11)
Phosphatidylcholines are the major phospholipid component of most eukaryotic cell membranes. Phosphatidylcholines have been shown to actively participate in regulatory and metabolic processes. Dysfunctional metabolic processes have been linked to human disease and can result in altered phosphatidylcholine structural features
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