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C105104

Sigma-Aldrich

2-Cyclohexylethanol

99%

Synonym(s):

(2-Hydroxyethyl)cyclohexane

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About This Item

Linear Formula:
C6H11CH2CH2OH
CAS Number:
4442-79-9
Molecular Weight:
128.21
Beilstein:
1848152
EC Number:
224-672-1
MDL number:
MFCD00001525
UNSPSC Code:
12352100
PubChem Substance ID:
24891959
NACRES:
NA.22

Quality Level

100

Assay

99%

form

liquid

refractive index

n20/D 1.465 (lit.)

bp

206-207 °C/745 mmHg (lit.)

density

0.919 g/mL at 25 °C (lit.)

SMILES string

OCCC1CCCCC1

InChI

1S/C8H16O/c9-7-6-8-4-2-1-3-5-8/h8-9H,1-7H2

InChI key

QJQZRLXDLORINA-UHFFFAOYSA-N

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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302 + H312

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

186.8 °F - closed cup

Flash Point(C)

86 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Rabea Schlüter et al.
Applied microbiology and biotechnology, 103(10), 4137-4151 (2019-04-04)
The cycloalkanes, comprising up to 45% of the hydrocarbon fraction, occur in crude oil or refined oil products (e.g., gasoline) mainly as alkylated cyclohexane derivatives and have been increasingly found in environmental samples of soil and water. Furthermore, short-chain alkylated
Qinglei Meng et al.
Nature communications, 8, 14190-14190 (2017-02-01)
Cyclohexanone and its derivatives are very important chemicals, which are currently produced mainly by oxidation of cyclohexane or alkylcyclohexane, hydrogenation of phenols, and alkylation of cyclohexanone. Here we report that bromide salt-modified Pd/C in H

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