Farnesene
Encyclopedia : F : FA : FAR : Farnesene
| Farnesene | |
|---|---|
 α-(E,E)-farnesene | |
| Chemical name | α: 3,7,11-trimethyl-1,3,6,10-dodecatetraene |
 β-(E)-farnesene | |
| Chemical name | β: 7,11-dimethyl-3-methylene-1,6,10-dodecatriene |
| Chemical formula | C15H24 |
| Molecular mass | 204.36 g/mol |
| CAS numbers | α-(E,E): [502-61-4] β-(E): [18794-84-8] β-(Z): [28973-97-9] |
| Densities | α-(E,E): 0.841 g/cm3 β-(E): 0.841 g/cm3 |
| Melting point | ? °C |
| Boiling points | α-(Z): 125 at 12 mmHg β-(E): 124 °C β-(Z): 95-107 at 3 mmHg |
| SMILES | α: CC(C)=CCCC(C)=CCC=C(C)C=C β: CC(C)=CCCC(C)=CCCC(C=C)=C |
| [Chemical infoboxDisclaimer and references] | |
The term farnesene refers to a set of closely related chemical compounds which are sesquiterpenes. α-Farnesene and β-farnesene are isomers, differing by the location of one double bond. α-Farnesene is 3,7,11-trimethyl-1,3,6,10-dodecatetraene and β-farnesene is 7,11-dimethyl-3-methylene-1,6,10-dodecatriene. The alpha form can exist as four stereoisomers that differ about the geometry of its two internal double bonds. The beta form can exist as two stereoisomers about the geometry of its central double bond.
α-(E,E)-Farnesene is the most common isomer. It is found the coating of apples, and other fruits, and its oxidation by air produces compounds that are damaging to the fruit. The oxidation products result in injury to cell membranes which eventually result in cell death in the outermost cell layers of the fruit, resulting in a storage disorder known as scald. α-(Z,E)-Farnesene has been isolated from the oil of perilla. Both isomers are also insect pheremones.
β-Farnesene has one naturally occurring isomer. The (E)-isomer is a constituent of various essential oils. It is also released by aphids as an alarm pheremone upon death to warn away other aphids. Several plants, including the wild potato have been shown to synthesize this pheromone as a natural insect repellent.
See also
References
- Gibson, R. W. & Pickett, J. A., "[Wild potato repels aphids by release of aphid alarm pheromone]", Nature 302, 608 - 609 (14 April 1983)
External links
- For a full list of external links to MSDSs, spectroscopic data, commercial chemicals suppliers etc. for this compound, see [Chemical sources].
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