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
ECHA InfoCard	100.020.268
EC Number	222-294-1
PubChem CID	103005;
	SMILES OC(CCC1)CC1C2CC3C(C)(C)C(C)C2C3;
Properties
Chemical formula	C16H28O
Molar mass	236.40 g·mol−1
Appearance	Colorless to pale yellow clear viscous liquid[1]
Density	0.97 g/mL[2]
Boiling point	302 °C (576 °F; 575 K)[2]
Hazards
R-phrases (outdated)	R36/38
S-phrases (outdated)	S26 S36
Flash point	110 °C (230 °F; 383 K) [2]
	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) 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,^[3] which are the primary constituents of sandalwood oil.

Sandalwood trees are endangered due to overharvesting,^[4] 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
1 2 3 3-(5,5,6-Trimethylbicyclo(2.2.1)hept-2-yl)cyclohexan-1-ol at Sigma-Aldrich
↑ Demole, Edouard (1964). "Synthesis and relations between chemical constitution and odor in the 3-terpenylcyclohexanol series". Helvetica Chimica Acta. 47 (7): 1766–74.
↑ Jean-Francois Tremblay (2011). "Rhodia Invests in Synthetic Sandalwood". Chemical & Engineering News. 89 (12): 24–25. doi:10.1021/CEN031511180238.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[good-1] Sandal hexanol at thegoodscentscompany.com

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

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

[CEN-4] Jean-Francois Tremblay (2011). "Rhodia Invests in Synthetic Sandalwood". Chemical & Engineering News. 89 (12): 24–25. doi:10.1021/CEN031511180238.