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Chemical compound From Wikipedia, the free encyclopedia
3,3,5-Trimethylcyclohexanol is a precursor to the vasodilator cyclandelate, the sunscreen component homosalate and the VP nerve agent.[1][2] It can be synthesized by hydrogenation of isophorone.[3] It has a mint flavour.
Names | |
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IUPAC name
3,3,5-trimethylcyclohexan-1-ol | |
Other names
Homomenthol | |
Identifiers | |
3D model (JSmol) |
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2203314 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.003.748 |
EC Number |
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PubChem CID |
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UNII |
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CompTox Dashboard (EPA) |
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Properties | |
C9H18O | |
Molar mass | 142.242 g·mol−1 |
Density | 0.878 at 20 °C |
Melting point | 37.0 °C (98.6 °F; 310.1 K) |
Boiling point | 198 °C (388 °F; 471 K) |
Hazards | |
GHS labelling: | |
Warning | |
H315, H319, H412 | |
P264, P273, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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