105899
Cyclohexanol
ReagentPlus®, 99%
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About This Item
Linear Formula:
C6H11OH
CAS Number:
Molecular Weight:
100.16
NACRES:
NA.21
PubChem Substance ID:
eCl@ss:
39023102
UNSPSC Code:
12352104
EC Number:
203-630-6
MDL number:
Beilstein/REAXYS Number:
906744
Assay:
99%
Bp:
160-161 °C (lit.)
Vapor pressure:
0.98 mmHg ( 25 °C)
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 %
dilution
(for general lab use)
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
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
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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
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
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 105899-3L | 04061838673251 |
| 105899-1L | 04061838673220 |
| 105899-25ML | 04061838673244 |