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Names | |||
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Preferred IUPAC name
Cyclohexanol | |||
Other names
Cyclohexyl Alcohol,
hexahydrophenol, hydrophenol, hydroxycyclohexane, Naxol Hexalin Hydralin HOCy | |||
Identifiers | |||
3D model (JSmol)
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3DMet | |||
ChEBI | |||
ChEMBL | |||
ChemSpider | |||
DrugBank | |||
ECHA InfoCard | 100.003.301 | ||
EC Number |
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KEGG | |||
PubChem CID
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RTECS number |
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UNII | |||
CompTox Dashboard (EPA)
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Properties | |||
C6H12O | |||
Molar mass | 100.158 g/mol | ||
Appearance | Colorless, viscous liquid. Hygroscopic | ||
Odor | camphor-like | ||
Density | 0.9624 g/mL, liquid | ||
Melting point | 25.93 °C (78.67 °F; 299.08 K) | ||
Boiling point | 161.84 °C (323.31 °F; 434.99 K) | ||
3.60 g/100 mL (20 °C) 4.3 g/100 mL (30 °C) | |||
Solubility | soluble in ethanol, ethyl ether, acetone, chloroform miscible with ethyl acetate, linseed oil, benzene | ||
Vapor pressure | 1 mmHg (20°C)[2] | ||
Henry's law
constant (kH) |
4.40 x 10−6 atm-cu m/mol | ||
Acidity (pKa) | 16 | ||
-73.40·10−6 cm3/mol | |||
Refractive index (nD)
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1.4641 | ||
Viscosity | 41.07 mPa·s (30 °C) | ||
Hazards | |||
Occupational safety and health (OHS/OSH): | |||
Main hazards
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Flammable, skin irritant Reacts violently with oxidizing agents | ||
GHS labelling: | |||
Warning | |||
H302, H315, H332, H335 | |||
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P321, P330, P332+P313, P362, P403+P233, P405, P501 | |||
NFPA 704 (fire diamond) | |||
Flash point | 67 °C (153 °F; 340 K) | ||
300 °C (572 °F; 573 K) | |||
Explosive limits | 2.7-12% | ||
Lethal dose or concentration (LD, LC): | |||
LD50 (median dose)
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2060 mg/kg (oral, rat) 2200-2600 mg/kg (oral, rabbit)[3] | ||
NIOSH (US health exposure limits): | |||
PEL (Permissible)
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TWA 50 ppm (200 mg/m3)[2] | ||
REL (Recommended)
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TWA 50 ppm (200 mg/m3)[2] | ||
IDLH (Immediate danger)
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400 ppm[2] | ||
Safety data sheet (SDS) | MSDS for cyclohexanol | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cyclohexanol is the organic compound with the formula HOCH(CH2)5. The molecule is related to cyclohexane by replacement of one hydrogen atom by a hydroxyl group.[4] This compound exists as a deliquescent colorless solid with a camphor-like odor, which, when very pure, melts near room temperature. Millions of tonnes are produced annually, mainly as a precursor to nylon.[5]