Chemistry:Rhodinol
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| Names | |
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| Preferred IUPAC name
(3S)-3,7-Dimethyloct-7-en-1-ol | |
| Other names
α-Citronellol, 3,7-Dimethyl-(6- or 7-)octen-1-ol, 3,7-Dimethyl-7-octen-1-ol, 1-Citronellol
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3D model (JSmol)
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| Properties | |
| C10H20O | |
| Molar mass | 156.269 g·mol−1 |
| Hazards | |
| GHS pictograms |   
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| GHS Signal word | Danger |
| H315, H317, H318, H319, H411 | |
| P261, P264, P272, P273, P280, P302+352, P305+351+338, P310, P321, P332+313, P333+313, P337+313, P362, P363, P391, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
Rhodinol is the chemical compound 3,7-dimethyloct-7-en-1-ol. As the (3S) isomer it is CAS 6812-78-8, and as the racemate it is CAS 141-25-3.
In the field of perfumery materials, the term may refer to L-citronellol, to mixtures comprising mostly L- or racemic citronellol and geraniol, or to mixtures comprising mostly racemic 3,7-dimethyloct-7-en-1-ol and racemic citronellol.
Two example synthetic Rhodinol products are Rhodinol 70, a racemic mixture comprising 40-60% 3,7-dimethyloct-7-en-1-ol and 40-60% citronellol, and Sigma-Aldrich Rhodinol, which consists of L-citronellol and geraniol.
Rhodinol is also provided in perfumery in natural grades as materials extracted from geranium or citronella, comprising principally citronellol and geraniol.
Rhodinol products are used in cosmetics and perfumery to impart flowery odors, particularly but not limited to being a component of rosy odor.[1]
3,7-Dimethyloct-7-en-1-ol does not appear substantively in nature.[2]
See also
- Citronellol
- Geraniol
- Perfume allergy
References
- ↑ Rhodinol The Good Scents Company
- ↑ The Citronellol Problem and the Isolation of α-Citronellol Journal of the American Chemical Society
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