O3880
Sodium oleate
≥95% (capillary GC)
Synonyme(s) :
cis-9-Octadecenoic acid sodium salt, Oleic acid sodium salt
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A propos de cet article
Formule linéaire :
CH3(CH2)7CH=CH(CH2)7COONa
Numéro CAS:
Poids moléculaire :
304.44
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
EC Number:
205-591-0
Beilstein/REAXYS Number:
4046357
MDL number:
Service technique
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Laissez-nous vous aiderbiological source
Olea europaea
assay
≥95% (capillary GC)
form
powder
mp
232-235 °C (lit.)
functional group
ester
lipid type
unsaturated FAs
shipped in
ambient
storage temp.
−20°C
SMILES string
[Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O
InChI
1S/C18H34O2.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20;/h9-10H,2-8,11-17H2,1H3,(H,19,20);/q;+1/p-1/b10-9-;
InChI key
BCKXLBQYZLBQEK-KVVVOXFISA-M
Application
Oleic acid is used to investigate effects on apolipoprotein B synthesis, degradation and secretion in cultured cells.
Biochem/physiol Actions
Activates protein kinase C in hepatocytes.
Oleic acid increases hepatic secretion of apolipoprotein B100 in hepatocyte cell lines and in mice . Oleic acid inhibits apolipoprotein B100 secretion at higher physiologic doses .
Classe de stockage
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Arno van der Weijden et al.
Nature communications, 11(1), 4800-4800 (2020-09-25)
Out-of-equilibrium molecular systems hold great promise as dynamic, reconfigurable matter that executes complex tasks autonomously. However, translating molecular scale dynamics into spatiotemporally controlled phenomena emerging at mesoscopic scale remains a challenge-especially if one aims at a design where the system
Zhengtao Liu et al.
American journal of translational research, 8(3), 1319-1338 (2016-05-18)
Epidemiological survey identified that the variant patatin-like phospholipase domain-containing protein 3 (PNPLA3) gene at I148M position exerts direct effect in promoting hepatocellular carcinoma (HCC) under extraneous oxidative stress by interaction with obesity. However, the mechanism is still unknown. HepG2 cells
Yoshikazu Kameshima et al.
International journal of pharmaceutics, 381(1), 34-39 (2009-08-04)
Mg-Al-ascorbic acid (ASA)-layered double hydroxides (ASA-LDHs) with Mg/Al=3 were synthesized by ion-exchange, coprecipitation and reconstruction methods. Composites with sodium oleate (SOA)/ASA-LDH were prepared by an ion-exchange method using various concentrations of SOA solutions. The (003) basal spacing of the ASA-LDHs