| Patchoulol |  |  | | IUPAC name | 3,4,4αβ,5,6β,7,8,8α-Octahydro-4α,8αβ,9,9- tetramethyl-1,6-methanonaphthalen-1β(2H)-ol | | Other names | Patchouli camphor; (–)-patchoulol; (1R,3R,6S,7S,8S)-patchoulol, patchouli alcohol | | Identifiers | | CAS number | 5986-55-0 | | EC number | 227-807-2 | | SMILES | O[C@@]23CC[C@@H]([C@@H]1C[C@@H](CC[C@@]12C)C3(C)C)C | | Properties | | Molecular formula | C15H26O | | Molar mass | 222.36 | | Appearance | Hexagonal-trapezohedral crystals | | Density | 1.0284 | | Melting point | 56 °C, 329 K, 133 °F 39-40 °C (racemic) | | Boiling point | 140 °C, 413 K, 284 °F | | Solubility in water | practically insoluble | | Solubility in ethanol | soluble | | Solubility in diethyl ether | soluble | | Refractive index (nD) | 1.5029 | | Hazards | | MSDS | External MSDS | | Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | | Infobox references | Patchoulol or patchouli alcohol (C15H26O) is a terpene extracted from Patchouli [1]. The (-)-optical isomer one of the organic compounds responsible for the typical patchouli scent. [edit] Toxicology [edit] See also [edit] External links - ^ Deguerry F., Pastore L., Wu S., Clark A., Chappell J., Schalk M. The diverse sesquiterpene profile of patchouli, Pogostemon cablin, is correlated with a limited number of sesquiterpene synthases(2006) Archives of Biochemistry and Biophysics, 454 (2), pp. 123-136.
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