4954

Oleic Acid

• Synonyme(s) : Oleic Acid, cis-9-Octadecenoic Acid, 18:1
• Formule empirique (notation de Hill) : C₁₈H₃₄O₂
• Numéro CAS: 112-80-1
• Poids moléculaire : 282.46
• UNSPSC Code: 12352211
• NACRES: NA.77
• MDL number: MFCD00064242
• Assay: ≥99% (GC)
• Form: liquid

Propriétés

• assay: ≥99% (GC)
• Quality Segment: 100
• form: liquid
• manufacturer/tradename: Calbiochem^®
• storage condition: OK to freeze
• color: colorless
• solubility: chloroform: 10 mg/mL, ethanol: 5 mg/mL
• density: 0.89 g/mL
• shipped in: ambient
• storage temp.: 2-8°C
• SMILES string: OC(=O)CCCCCCC\C=C\CCCCCCCC
• InChI: 1S/C18H34O2/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)/b10-9+
• InChI key: ZQPPMHVWECSIRJ-MDZDMXLPSA-N

Description

General description

A cis-unsaturated fatty acid that has been shown to activate protein kinase C in hepatocytes. Potentiates acetylcholine receptor currents by activating CaM kinase II, independent of the PKC pathway.

Unsaturated fatty acid that has been shown to activate protein kinase C in hepatocytes. Density: 0.89 g/ml.

Biochem/physiol Actions

Cell permeable: no

Product does not compete with ATP.

Reversible: no

Packaging

Packaged under inert gas

Other Notes

Nishizaki, T., et al. 1997. NeuroReport 8, 597.
Bessesen, D.H., et al. 1993. J. Lipid Res.34, 229.
Felden, F., et al. 1993. Biochem. Biophys. Res. Commun.190, 602.
Williams, L.L., et al. 1993. Proc. Soc. Exp. Biol. Med.202, 239.
Diaz-Guerra, M.J. 1991. J. Biol. Chem.266, 23568.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)

Informations sur la sécurité

• Classe de stockage: 10 - Combustible liquids
• wgk: WGK 1
• flash_point_f: >235.4 °F - closed cup
• flash_point_c: > 113 °C - closed cup