Citronellol
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| Template:Longitem | 1362474 |
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| Density | 0.855 g/cm3 |
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| Viscosity | 11.1 mPa s |
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Citronellol, or dihydrogeraniol, is a natural acyclic monoterpenoid. Both enantiomers occur in nature. (+)-Citronellol, which is found in citronella oils, including Cymbopogon nardus (50%), is the more common isomer. (−)-Citronellol is widespread, but particularly abundant in the oils of rose (18–55%) and Pelargonium geraniums.[1]
Preparation
Several million kilograms of citronellol are produced annually. It is mainly obtained by partial hydrogenation of geraniol or nerol over copper chromite catalyst.[2] Hydrogenation of both C=C bonds using a nickel catalyst gives tetrahydrogeraniol, yet another commercial fragrance.[3]
Homogeneous catalysts have been investigated for the production of enantiomers.[4][5]
Uses
Citronellol is used in perfumes and as a fragrance in cleaning products. In many applications, one of the enantiomers is preferred. It is a component of citronella oil, an insect repellant.[2]
Citronellol is used as a raw material for the production of rose oxide.[2][6] It is also a precursor to many commercial and potential fragrances such as citronellol acetate, citronellyl oxyacetaldehyde, citronellyl methyl acetal, and ethyl citronellyl oxalate.[2]
Health and safety
The United States FDA considers citronellol as generally recognized as safe (GRAS) for food use.[7] Citronellol is subject to restrictions on its use in perfumery,[8] as some people may become sensitised to it, but the degree to which citronellol can cause an allergic reaction in humans is disputed.[9][10]
In terms of dermal safety, citronellol has been evaluated as an insect repellent.[11]
See also
References
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- ↑ Survey and health assessment of chemical substances in massage oils Template:Webarchive
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