Isobornyl cyclohexanol

Isobornyl cyclohexanol
Names
	IUPAC name 3-(5,5,6-Trimethylbicyclo[2.2.1]heptan-2-yl)cyclohexanol
	Other names Isocamphyl cyclohexanol; 3-[5,5,6-Trimethylbicyclo[2.2.1]hept-2-yl]cyclohexan-1-ol; Sandal hexanol
Identifiers
CAS Number	3407-42-9 ;
3D model (JSmol)	Interactive image;
Abbreviations	IBCH
ChEBI	CHEBI:171884;
ChEMBL	ChEMBL3182308;
ChemSpider	93057;
ECHA InfoCard	100.020.268
EC Number	222-294-1222-294-1;
PubChem CID	103005;
UNII	34UP96K73Z ;
CompTox Dashboard (EPA)	DTXSID5044817 ;
	SMILES OC(CCC1)CC1C2CC3C(C)(C)C(C)C2C3;
Properties
Chemical formula	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:
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H411, H412
Precautionary statements	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). verify (what is ?) Infobox references

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,^[4] which are the primary constituents of sandalwood oil.

Sandalwood trees are endangered due to overharvesting,^[5] leading to a high cost for the natural oil. IBCH is therefore produced as an economical alternative to the natural product.

References

^ Sandal hexanol at thegoodscentscompany.com
^ ^a ^b ^c 3-(5,5,6-Trimethylbicyclo(2.2.1)hept-2-yl)cyclohexan-1-ol at Sigma-Aldrich
^ GHS: PubChem 103005
^ Demole, Edouard (1964). "Synthesis and relations between chemical constitution and odor in the 3-terpenylcyclohexanol series". Helvetica Chimica Acta. 47 (7): 1766–74. doi:10.1002/hlca.19640470713.
^ Jean-Francois Tremblay (2011). "Rhodia Invests in Synthetic Sandalwood". Chemical & Engineering News. 89 (12): 24–25. doi:10.1021/CEN031511180238.

[good-1] Sandal hexanol at thegoodscentscompany.com

[SA-2] 3-(5,5,6-Trimethylbicyclo(2.2.1)hept-2-yl)cyclohexan-1-ol at Sigma-Aldrich

[3] GHS: PubChem 103005

[4] Demole, Edouard (1964). "Synthesis and relations between chemical constitution and odor in the 3-terpenylcyclohexanol series". Helvetica Chimica Acta. 47 (7): 1766–74. doi:10.1002/hlca.19640470713.

[CEN-5] Jean-Francois Tremblay (2011). "Rhodia Invests in Synthetic Sandalwood". Chemical & Engineering News. 89 (12): 24–25. doi:10.1021/CEN031511180238.

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