Isobornyl cyclohexanol
| Names | |
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| IUPAC name
3-(5,5,6-Trimethylbicyclo[2.2.1]heptan-2-yl)cyclohexanol
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| Other names
Isocamphyl cyclohexanol; 3-[5,5,6-Trimethylbicyclo[2.2.1]hept-2-yl]cyclohexan-1-ol; Sandal hexanol
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| Identifiers | |
3D model (JSmol)
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| Abbreviations | IBCH |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.020.268 |
| EC Number |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C16H28O | |
| Molar mass | 236.399 g·mol−1 |
| Appearance | Colorless to pale yellow clear viscous liquid |
| Density | 0.97 g/mL |
| Boiling point | 302 °C (576 °F; 575 K) |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H315, H319, H411, H412 | |
| P264, P273, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362, P391, P501 | |
| Flash point | 110 °C (230 °F; 383 K) |
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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Isobornyl cyclohexanol (IBCH, Sandenol) is an organic compound used primarily as a fragrance because of its aroma which is similar to sandalwood oil. Its chemical structure is closely related to that of both α-santalol and β-santalol, which are the primary constituents of sandalwood oil.
Sandalwood trees are endangered due to overharvesting, leading to a high cost for the natural oil. IBCH is therefore produced as an economical alternative to the natural product.