Provenance

Reference data from EU CLP Annex VI and published regulations — verify against your supplier's SDS before use.

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Substance profile

Cyclohexanol

Cyclohexanol is colorless needles or viscous liquid with a camphor-like odor.

CAS 108-93-0 C6H12O 100.16 g/mol Warning

01 · Identification

What Cyclohexanol is

Cyclohexanol is colorless needles or viscous liquid with a camphor-like odor. Its molecular formula is C6H12O and its molecular weight is 100.16 g/mol. It boils at 162 °C, melts at 25.9 °C.

Under the GHS it carries the signal word Warning. It is classed as flammable agents - 2nd degree.

CAS number108-93-0
EC number203-630-6
Index number603-009-00-3
Molecular formulaC6H12O
Molecular weight100.16 g/mol
Chemical class Flammable agents - 2nd degree

02 · GHS classification

Hazards and label elements

Harmonised classification under CLP Annex VI. This is the legally binding classification in the EU; other jurisdictions may differ.

Signal wordWarning
Hazard statements assigned to Cyclohexanol
CodeHazard statement
H332 Harmful if inhaled.
H302 Harmful if swallowed.
H335 May cause respiratory irritation.
H315 Causes skin irritation.

Precautionary statements: P260, P264, P270, P271, P280, P301, P302, P304, P312, P313, P330, P332, P352

03 · Physical and chemical properties

Cyclohexanol properties

Every value is shown with the conditions it was measured under and the source it came from. Where sources disagree, all values are listed rather than one being picked — the difference is usually a different form of the substance, not an error.

Property Value Conditions Source
Boiling point 161.84 °C (323.3 °F) HSDB
161.11 °C (322 °F) NIOSH
161.11 °C (322 °F) at 760 mmHg CAMEO
Melting point 25.93 °C (78.7 °F) HSDB
25 °C (77 °F) NIOSH
22.78 °C (73 °F) CAMEO
Density 0.96 g/cm³ NIOSH
0.9624 g/cm³ at 20 °C HSDB
0.947 g/cm³ at 20 °C CAMEO
Solubility Soluble in ethanol, ethyl ether, acetone; miscible with benzene; slightly soluble in chloroform HSDB
4% NIOSH
3.6% (wt/wt) in water at 20 °C; miscible with ethyl acetate, linseed oil, petroleum solvents. at 20 °C HSDB
Vapor pressure 1 mmHg NIOSH
1.1251 mmHg at 20 °C HSDB
0.657 mmHg at 25 °C HSDB
Flash point 62.8 °C (145 °F) closed cup HSDB
67.78 °C (154 °F) NIOSH
Autoignition temperature 300 °C (572 °F) HSDB
Lower explosive limit (LEL) 2.7 % by volume HSDB
2.4 % by volume ICSC
Above 68 °C explosive vapor/air mixtures may be formed. HSDB
Upper explosive limit (UEL) 12 % by volume HSDB
Vapor density 3.5 (air = 1) HSDB
Odor threshold 0.07 ppm HSDB
Odor Threshold Low: 0.05 [ppm] Haz-Map
Odor Threshold High: 0.15 [ppm] Haz-Map
Critical temperature and pressure 376.95 °C (710.5 °F) HSDB

Values compiled from PubChem Laboratory Chemical Safety Summary. Temperatures converted to Fahrenheit for reference.

04 · Handling and storage

Storing and handling Cyclohexanol

Storage conditions

Cyclohexanol must be stored to avoid contact with strong oxidizers (such as chlorine, bromine, and fluorine), since violent reactions occur. Metal containers involving the transfer of this chemical should be grounded and bonded. Where possible, automatically pump liquid from drums or other storage containers to process containers. Drums must be equipped with self-closing valves, pressure vacuum bungs, and flame arresters. Use only non-sparking tools and equipment, especially when opening and closing containers of this chemical. Sources of ignition, such as smoking and open flames, are prohibited where this chemical is used, handled, or stored in a manner that could created a potential fire or explosion hazard. Wherever this chemical is used, handled, manufactured, or stored, use explosion-proof electrical equipment and fittings.

Source: Hazardous Substances Data Bank (HSDB)

Incompatible materials

Contact with strong oxidizers causes a fire and explosion hazard. Attacks some plastics.

Source: Hazardous Substances Data Bank (HSDB)

Reactivity

CYCLOHEXANOL is an alcohol. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides. Violent reaction with nitric acid. Incompatible with strong oxidizers (chromium trioxide, nitric acid, etc.). (NTP, 1992)

Source: CAMEO Chemicals

Planning storage for a mix of chemicals? Check Cyclohexanol in the storage compatibility matrix →

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