Cyclohexanol
Names | |
---|---|
IUPAC name
Cyclohexanol
| |
Systematic IUPAC name
Cyclohexanol | |
Other names
Cyclohexyl alcohol
CyOH Hexahydrophenol Hexalin Hydralin Hydrophenol Hydroxycyclohexane Naxol | |
Properties | |
C6H12O (CH2)5CHOH | |
Molar mass | 100.158 g/mol |
Appearance | Colorless viscous liquid |
Odor | Camphor-like |
Density | 0.9624 g/cm3 (20 °C) |
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 | Misicble with acetone, benzene, chloroform, diethyl ether, ethanol, ethyl acetate, linseed oil, toluene, xylene |
Vapor pressure | 1 mmHg (20 °C) |
Acidity (pKa) | 16 |
Thermochemistry | |
Hazards | |
Safety data sheet | Sigma-Aldrich |
Flash point | 67 °C (153 °F; 340 K) |
Lethal dose or concentration (LD, LC): | |
LD50 (Median dose)
|
1,400 mg/kg (rat, oral) 2,200-2,600 mg/kg (rabbit, oral) |
Related compounds | |
Related compounds
|
Cyclopentanol Cycloheptanol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Cyclohexanol is the organic compound with the formula (CH2)5CHOH
Contents
Properties
Chemical
Oxidation of cyclohexanol yields cyclohexanone.
Physical
Cyclohexanol is a colorless solid at room temperature, that rapidly melts into a viscous liquid upon gentle heating. It has a camphor-like odor and miscible with organic solvents.
Availability
Cyclohexanol is sold by chemical suppliers. Can also be bought online.
Preparation
Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts:
- C6H12 + ½ O2 → C6H11OH
This process co-forms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid. The oxidation involves radicals and the intermediacy of the hydroperoxide C6H11O2H.
Alternatively, cyclohexanol can be produced by the hydrogenation of phenol, using nickel catalyst:[1]
- C6H5OH + 3 H2 → C6H11OH
This process can also be adjusted to favor the formation of cyclohexanone and cyclohexane.
Projects
- Make adipic acid and nylon
- Make cyclohexanone
Handling
Safety
Cyclohexanol is somewhat toxic: the TLV for the vapor for 8 h is 50 ppm. The IDLH concentration is set at 400 ppm, based on studies on the acute oral toxicity in animals.
Due to its high flash point of 67 °C, cyclohexanol is not very flammable and poses a moderate fire hazard.
Storage
Cyclohexanol should be kept in closed bottles, away from oxidizers and flames.
Disposal
Should be mixed with a more flammable solvent and incinerated.