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105899

Sigma-Aldrich

Cyclohexanol

ReagentPlus®, 99%

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Linear Formula:
C6H11OH
CAS Number:
Molecular Weight:
100.16
Beilstein:
906744
EC Number:
MDL number:
UNSPSC Code:
12352104
eCl@ss:
39023102
PubChem Substance ID:
NACRES:
NA.21

vapor density

3.5 (vs air)

Quality Level

vapor pressure

0.98 mmHg ( 25 °C)

product line

ReagentPlus®

Assay

99%

autoignition temp.

572 °F

expl. lim.

12.25 %

refractive index

n20/D 1.465 (lit.)

bp

160-161 °C (lit.)

mp

20-22 °C (lit.)

density

0.948 g/mL at 25 °C (lit.)

SMILES string

OC1CCCCC1

InChI

1S/C6H12O/c7-6-4-2-1-3-5-6/h6-7H,1-5H2

InChI key

HPXRVTGHNJAIIH-UHFFFAOYSA-N

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General description

Cyclohexanol is an alicyclic alcohol. It is industrially produced from phenol, via hydrogenation in the presence of Ni/Al2O3 catalyst. It is also produced from cyclohexane, via oxidation with molecular oxygen in the presence of Co3O4 nanocrystals (catalyst). A mixture of cyclohexanone (K) and cyclohexanol (A) is known as KA oil. KA oil can be generated from cyclohexane, via liquid-phase oxidation.

Application

Cyclohexanol may be used in the preparation of ε-caprolactam and adipic acid, important precursors for the industrial synthesis of nylon-6 and nylon-6.6, respectively.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 1

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Cyclohexanol-1-13C 99 atom % 13C

Sigma-Aldrich

492086

Cyclohexanol-1-13C

Nazanin Vafaei et al.
Applied biochemistry and biotechnology, 191(3), 905-920 (2020-01-11)
The time course study of high monoester mixtures from soybean oil (HMMS) synthesis, as healthier alternatives to trans food products, in a supercritical CO2 (SCCO2) medium with and without enzyme, was investigated. Phosphorous nuclear magnetic resonance (31P-NMR) was used to
Eagleson M.
Concise Encyclopedia Chemistry, 811-811 (1994)
Catalytic oxidation of cyclohexane to cyclohexanol and cyclohexanone over Co3O4 nanocrystals with molecular oxygen.
Zhou L, et al.
Applied Catalysis A: General, 292, 223-228 (2005)
Eagleson M.
Concise Encyclopedia Chemistry, 511-511 (1994)
Kinetic model of 2-cyclohexenone formation from cyclohexanol and 2-cyclohexenol dehydrogenation.
Simon E, et al.
Chemical Engineering Journal, 192, 129-137 (2012)

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