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Contents

   



(Top)
  


1 See also  




2 References  













3,3,5-Trimethylcyclohexanol






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From Wikipedia, the free encyclopedia
  

3,3,5-Trimethylcyclohexanol
Names
IUPAC name

3,3,5-trimethylcyclohexan-1-ol

Other names

Homomenthol

Identifiers

CAS Number
  • trans: 767-54-4
  • cis: 933-48-2 checkY

    • 3D model (JSmol)

    Beilstein Reference

    		 2203314
    ChEBI
    ChEMBL
    ChemSpider
    ECHA InfoCard 100.003.748 Edit this at Wikidata
    EC Number
    • 204-122-7
  • trans: 212-183-6
  • cis: 213-268-0

    • PubChem CID
    UNII
  • cis: 3T046ESA4Q checkY

    • CompTox Dashboard (EPA)

    • InChI=1S/C9H18O/c1-7-4-8(10)6-9(2,3)5-7/h7-8,10H,4-6H2,1-3H3

      Key: BRRVXFOKWJKTGG-UHFFFAOYSA-N

    • CC1CC(CC(C1)(C)C)O

    Properties

    Chemical formula

    		 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:

    Pictograms

    		 GHS07: Exclamation mark

    Signal word

    		 Warning

    Hazard statements

    		 H315, H319, H412

    Precautionary statements

    		 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).

    Infobox references

    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 hydrogenationofisophorone.[3] It has a mint flavour.

    See also[edit]

    References[edit]

    1. ^ Bell, GD; Clegg, RJ; Ellis, WR; Middleton, B; White, DA (January 1984). "The effects of 3,5,5-trimethylcyclohexanol on hepatic cholesterol synthesis, bile flow and biliary lipid secretion in the rat". British Journal of Pharmacology. 81 (1): 183–7. doi:10.1111/j.1476-5381.1984.tb10759.x. PMC 1986967. PMID 6704580.
  • ^ "3-Pyridyl phosphonates". US3903098A.
  • ^ "Fragrance raw materials monographs". Food and Cosmetics Toxicology. 12 (7–8): 1007. December 1974. doi:10.1016/0015-6264(74)90227-2.


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  • t
  • e

    • Retrieved from "https://en.wikipedia.org/w/index.php?title=3,3,5-Trimethylcyclohexanol&oldid=999809727"
    Categories: 
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