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105899

Sigma-Aldrich

Cyclohexanol

ReagentPlus®, 99%

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About This Item

Linear Formula:
C6H11OH
CAS Number:
108-93-0
Molecular Weight:
100.16
Beilstein:
906744
EC Number:
203-630-6
MDL number:
MFCD00003855
UNSPSC Code:
12352104
eCl@ss:
39023102
PubChem Substance ID:
24846712
NACRES:
NA.21

vapor density

3.5 (vs air)

Quality Level

200

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
GHS07

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

147.2 °F - closed cup - DIN 51794

Flash Point(C)

64 °C - closed cup - DIN 51794

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF3610V
WXBF0313V
WXBF1603V
WXBD7641V
WXBD8681V

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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
Kinetic model of 2-cyclohexenone formation from cyclohexanol and 2-cyclohexenol dehydrogenation.
Simon E, et al.
Chemical Engineering Journal, 192, 129-137 (2012)
Cong Gao et al.
International journal of biological macromolecules, 162, 1642-1652 (2020-08-17)
The low cost, environmental friendliness, and reproducibility of kraft lignin (KL) make it a potential candidate for the development of new green material. The phosphorylation of KL can extend its application as a flame-retardant material. Herein, the phosphorylated kraft lignin
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)
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