Cyclohexanol
Cyclohexanol is an organic compound with the molecular formula C6H12O.
- Formula
- C6H12O
- Functional group
- Secondary alcohols
- Molar mass
- 100.16 g/mol
- Also known as
- Cyclohexyl alcohol, 1-Cyclohexanol, Hexahydrophenol, Hydrophenol, Hydroxycyclohexane, Hexalin
Overview
Cyclohexanol is an organic compound with the molecular formula C6H12O.
Identifiers
- Formula
- C6H12O
- Functional group
- Secondary alcohols
- Molar mass
- 100.16 g/mol
- Also known as
- Cyclohexyl alcohol, 1-Cyclohexanol, Hexahydrophenol, Hydrophenol, Hydroxycyclohexane, Hexalin
Chemical identifiers
- SMILES
- C1CCC(CC1)O
- InChI
- InChI=1S/C6H12O/c7-6-4-2-1-3-5-6/h6-7H,1-5H2
- PubChem CID
- 7966
Properties
- Melting Point
- 25.93 °C
- Boiling Point
- 161.84 °C
- Relative density (water = 1)
- Relative density (water = 1): 0.96
- Water solubility
- In water, 4.3 g/100 g (4.3X10+4 mg/L) at 30 °C; 4.2 g/100 g (4.2X10+4 mg/L) at 10 °C
Related compounds
- Alcohols
Cyclohexanol is an organic compound with the molecular formula C6H12O.
- Secondary alcohols
Cyclohexanol is an organic compound with the molecular formula C6H12O.
Connected reactions
- Dehydration: Cyclohexanol → Cyclohexene
Cyclohexanol gives cyclohexene through dehydration.
- Secondary alcohol oxidation: Cyclohexanol → Cyclohexanone
Oxidation removes hydrogen from the O-H group and its attached carbon, creating a C=O bond. Because that carbon already bonds to two other carbons, the product is a ketone and the six-membered ring is retained.
- Ketone reduction: Cyclohexanone → Cyclohexanol
Hydride adds to the planar carbonyl carbon while the pi electrons move onto oxygen. Subsequent protonation gives cyclohexanol; the existing carbon ring remains intact.
References
- PubChem Compound Summary: Cyclohexanol (CID 7966)National Center for Biotechnology Information · PubChem
Identity, molecular formula, molecular weight and aliases retrieved via PUG REST on 2026-09-08.
- Hazardous Substances Data Bank (HSDB): Cyclohexanol — melting pointHazardous Substances Data Bank (HSDB)
Retrieved through PubChem PUG View on 2026-09-08. https://pubchem.ncbi.nlm.nih.gov/compound/7966#section=Melting-Point. Source value, complete property clause or compact miscibility statement retained; absent pressure, temperature or phase conditions are not inferred. Original reference: Lide, D.R. CRC Handbook of Chemistry and Physics 88TH Edition 2007-2008. CRC Press, Taylor & Francis, Boca Raton, FL 2007, p. 3-128
- Hazardous Substances Data Bank (HSDB): Cyclohexanol — boiling pointHazardous Substances Data Bank (HSDB)
Retrieved through PubChem PUG View on 2026-09-08. https://pubchem.ncbi.nlm.nih.gov/compound/7966#section=Boiling-Point. Source value, complete property clause or compact miscibility statement retained; absent pressure, temperature or phase conditions are not inferred. Original reference: Lide, D.R. CRC Handbook of Chemistry and Physics 88TH Edition 2007-2008. CRC Press, Taylor & Francis, Boca Raton, FL 2007, p. 3-128
- ILO-WHO International Chemical Safety Cards (ICSCs): Cyclohexanol — densityILO-WHO International Chemical Safety Cards (ICSCs)
Retrieved through PubChem PUG View on 2026-09-08. https://pubchem.ncbi.nlm.nih.gov/compound/7966#section=Density. Source value, complete property clause or compact miscibility statement retained; absent pressure, temperature or phase conditions are not inferred.
- Hazardous Substances Data Bank (HSDB): Cyclohexanol — solubilityHazardous Substances Data Bank (HSDB)
Retrieved through PubChem PUG View on 2026-09-08. https://pubchem.ncbi.nlm.nih.gov/compound/7966#section=Solubility. Source value, complete property clause or compact miscibility statement retained; absent pressure, temperature or phase conditions are not inferred. Original reference: Fisher WB, VanPeppen JF; Kirk-Othmer Encyclopedia of Chemical Technology. (2001). New York, NY: John Wiley & Sons; Cyclohexanol and Cyclohexanone. Online Posting Date: December 4, 2009.