Patchoulol
| Names | |
|---|---|
| Preferred IUPAC name
(1R,4S,4aS,6R,8aS)-4,8a,9,9-Tetramethyldecahydro-1,6-methanonaphthalen-1-ol | |
| Other names
Patchouli camphor;
(−)-Patchoulol; (1R,3R,6S,7S,8S)-Patchoulol; Patchouli alcohol | |
| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.025.279 |
| EC Number |
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| KEGG | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C15H26O | |
| Molar mass | 222.36 |
| Appearance | white solid |
| Density | 1.0284 g/mL |
| Melting point | 56 °C (133 °F; 329 K) (racemic) |
| Boiling point | 287–288 °C (549–550 °F; 560–561 K) |
| practically insoluble | |
| Solubility in ethanol | soluble |
| Solubility in diethyl ether | soluble |
Refractive index (nD)
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1.5029 |
| Hazards | |
| Safety data sheet (SDS) | External MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Patchoulol or patchouli alcohol (C15H26O) is a sesquiterpene alcohol found in patchouli (Pogostemon cablin). Patchouli oil is an important material in perfumery. The (−)-optical isomer is one of the organic compounds responsible for the typical patchouli scent. Patchoulol is obtained industrially from patchouli leaf fermentation.
Patchoulol is also used in the synthesis of the chemotherapy drug Taxol.