Lesquerolic acid
Jump to navigation
Jump to search
| |
| Names | |
|---|---|
| Preferred IUPAC name
(11Z,14R)-14-Hydroxyicos-11-enoic acid[1] | |
| Identifiers | |
3D model (JSmol)
|
|
| ChemSpider | |
| MeSH | lesquerolic+acid |
PubChem CID
|
|
| UNII | |
| |
| |
| Properties | |
| C20H38O3 | |
| Molar mass | 326.521 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Lesquerolic acid is a hydroxycarboxylic acid that occurs naturally in Paysonia lasiocarpa and other Paysonia and Physaria species.[2] This compound has the R configuration at the alcohol-bearing stereocenter, and it is of the Z configuration at the olefin. Lesquerolic acid is chemically similar to ricinoleic acid, but with two additional carbons at the carboxyl end of the carbon chain.[3] Lesquerolic acid, with other hydroxy fatty acids, has important industrial uses, including making resins, waxes, nylons and plastics.
References
- ^ "CID 20980884 - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 5 December 2007. Retrieved 20 November 2011.
- ^ C. R. Smith Jr.; T. L. Wilson; T. K. Miwa; H. Zobel; R. L. Lohmar; I. A. Wolff (1961). "Lesquerolic Acid. A New Hydroxy Acid from Lesquerella Seed Oil1a". J. Org. Chem. 26 (8): 2903–2905. doi:10.1021/jo01066a067.
- ^ David A. Dierig (1995). "Lesquerella". New Crop FactSHEET.
 | This article about an alkene is a stub. You can help Wikipedia by expanding it. |