For research use only. Not for therapeutic Use.
| CAS Number | 629-22-1 |
| Synonyms | 2-Hydroxy C18:0 fatty acid |
| Molecular Formula | C18H36O3 |
| Purity | ≥95% |
| Solubility | chloroform/methanol, 5:1 |
| Storage | Store at -20°C |
| IUPAC Name | 2-hydroxyoctadecanoic acid |
| InChI | InChI=1S/C18H36O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(19)18(20)21/h17,19H,2-16H2,1H3,(H,20,21) |
| InChIKey | KIHBGTRZFAVZRV-UHFFFAOYSA-N |
| SMILES | CCCCCCCCCCCCCCCCC(C(=O)O)O |
| Reference | <br>1. C. Lendrum et al. “Nonequilibrium 2-Hydroxyoctadecanoic Acid Monolayers: Effect of Electrolytes” Langmuir, vol. 27 pp. 4430-4438, 2011<br>2. E. Maldonado et al. “FA2H is responsible for the formation of 2-hydroxy galactolipids in peripheral nervous system myelin” Journal of Lipid Research, Vol. 49 pp. 153-161, 2008<br>3. G. Nagahashi and D. Douds Jr. “The effects of hydroxy fatty acids on the hyphal branching of germinated spores of AM fungi” Fungal Biology, vol. 115 pp. 351-358, 2011<br>4. R. Sandhir, M. Khan, and I. Singh “Identification of the Pathway of alpha-Oxidation of Cerebronic Acid in Peroxisomes” Lipids, Vol. 35(10) pp. 1127-1133, 2000<br>5. T. Kaneshiro et al. “2-Hydroxyhexadecanoic and 8,9,13-trihydroxydocosanoic acid accumulation by yeasts treated with fumonisin B1” Lipids, vol. 28 pp. 397-401, 1993</br></br></br></br></br> |
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