α-Vetivone
Appearance
(Redirected from Vetivone)
Names | |
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IUPAC name
4α,5α-Eremophila-1(10),7(11)-dien-2-one
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Systematic IUPAC name
(4R,4aS)-4,4a-Dimethyl-6-(propan-2-ylidene)-4,4a,5,6,7,8-hexahydronaphthalen-2(3H)-one | |
Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.036.217 |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C15H22O | |
Molar mass | 218.335 |
Appearance | colourless solid |
Density | 0.962 g/mL |
Boiling point | 270.5 °C (518.9 °F; 543.6 K) |
practically insoluble | |
Solubility in ethanol | soluble |
Solubility in diethyl ether | soluble |
Related compounds | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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α-Vetivone is an organic compound that is classified as a sesquiterpene (derived from three isoprene units). It is a major component of the oil of vetiver, which is used to prepare certain high value perfumes.
α-Vetivone is isolated by steam distillation of the roots of the grass Vetiveria zizanioides. Two other components of this distillate are the sesquiterpenes khusimol and β-vetivone shown below.[1]
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Structure of khusimol, another fragrant component of the oil of vetiver.
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Structure of β-vetivone, another fragrant component of the oil of vetiver.
References
[edit]- ^ Karl-Georg Fahlbusch, Franz-Josef Hammerschmidt, Johannes Panten, Wilhelm Pickenhagen, Dietmar Schatkowski, Kurt Bauer, Dorothea Garbe, Horst Surburg "Flavors and Fragrances" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim: 2002. Published online: 15 January 2003; doi:10.1002/14356007.a11_141.