Exocarpic acid
| Names | |
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| IUPAC name
(E)-octadec-13-en-9,11-diynoic acid | |
| Other names
Octadeca-trans-13-ene-9,11-diynoic acid | |
| Identifiers | |
3D model (JSmol) |
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| Properties | |
| C18H26O2 | |
| Molar mass | 274.404 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Exocarpic acid is an unsaturated, conjugated fatty acid with one double bond and two triple bonds. It is isomeric to isanic acid and belongs to the class of alkyne and alkenoic acids, as well as the diynes and enynes. The acid's delta notation is 18:3-delta-9a,11a,13t. Its structural formula is CH 3(CH2)3-CH=CH-C≡CC≡C-(CH2)7-COOH.
The acid was initially isolated in 1959, by H. H. Hatt and co-workers, from the roots of the Australian tree Exocarpos cupressiformis; from this genus they derived the common name of exocarpic acid.