Vernolic acid
(−)-(12R,13S)-EpOME | |
| Names | |
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| Preferred IUPAC name
(9Z)-(12S,13R)-12,13-epoxyoctadecenoic acid | |
| Other names
Racemic:
Single-enantiomer (corresponding to IUPAC-name isomer):
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| Identifiers | |
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3D model (JSmol) |
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| ChEBI |
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| ChemSpider | |
PubChem CID |
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| UNII |
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CompTox Dashboard (EPA) |
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| Properties | |
| C18H32O3 | |
| Molar mass | 296.451 g·mol−1 |
| Appearance | Colorless oil |
| Melting point | 23 to 25 °C (73 to 77 °F; 296 to 298 K) |
| Insoluble | |
| Solubility in other solvents | organic solvents |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards |
flammable |
| Related compounds | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Vernolic acid (leukotoxin B or isoleukotoxin) is a long chain fatty acid that is monounsaturated and contains an epoxide. It is a cis epoxide derived from the C12–C13 alkene of linoleic acid. Vernolic acid was first definitively characterized in 1954 and its absolute configuration determined in 1966. It is a major component in vernonia oil, which is produced in abundance by the genera Vernonia and Euphorbia and is a potentially useful biofeedstock.