8-Hydroxygeraniol
| Names | |
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| Preferred IUPAC name
(2E,6E)-2,6-Dimethylocta-2,6-diene-1,8-diol | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.209.637 |
| KEGG | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C10H18O2 | |
| Molar mass | 170.252 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
8-Hydroxygeraniol (also incorrectly called 10-hydroxygeraniol) is a monoterpene synthesized from geraniol by the enzyme geraniol 8-hydroxylase. 8-Hydroxygeraniol is a substrate for 8-hydroxygeraniol dehydrogenase (G80) which synthesizes 8-oxogeranial. 8-Hydroxygeraniol is an intermediate in the synthesis of the secologanin, a key monoterpene needed for formation of terpene indole alkaloids.
In the laboratory, 8-hydroxygeraniol can be prepared from geranyl acetate.