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Citronellol, or dihydrogeraniol, is a natural acyclic mono. Both occur in nature. (+)-Citronellol, which is found in , including Cymbopogon nardus (50%), is the more common isomer. (−)-Citronellol is widespread, but particularly abundant in the oils of (18–55%) and geraniums.

(1995). 9781852306618


Preparation
Several million kilograms of citronellol are produced annually. It is mainly obtained by partial of or over catalyst.
(2025). 9780471238966
Hydrogenation of both C=C bonds using a nickel catalyst gives tetrahydro, yet another commercial fragrance.
(2025). 9783527306732

Homogeneous catalysts have been investigated for the production of .

(2025). 9783527311613, Wiley-VCH.


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.

Citronellol is used as a raw material for the production of . It is also a precursor to many commercial and potential fragrances such as citronellol acetate, citronellyl oxyacetaldehyde, citronellyl methyl acetal, and ethyl citronellyl oxalate.


Health and safety
The United States FDA considers citronellol as generally recognized as safe (GRAS) for food use. Citronellol is subject to restrictions on its use in perfumery, as some people may become sensitised to it, but the degree to which citronellol can cause an allergic reaction in humans is disputed. Survey and health assessment of chemical substances in massage oils

In terms of dermal safety, citronellol has been evaluated as an insect repellent.


See also

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