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E19154

Sigma-Aldrich

Ethylcyclohexane

≥99%

Synonym(s):

ECH

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About This Item

Linear Formula:
C6H11C2H5
CAS Number:
1678-91-7
Molecular Weight:
112.21
Beilstein:
1900337
EC Number:
216-835-0
MDL number:
MFCD00001523
UNSPSC Code:
12352100
PubChem Substance ID:
24894446
NACRES:
NA.22

vapor pressure

25 mmHg ( 37.7 °C)

Quality Level

100

Assay

≥99%

form

liquid

autoignition temp.

504 °F

expl. lim.

6.6 %

refractive index

n20/D 1.432 (lit.)

bp

130-132 °C (lit.)

mp

−111 °C (lit.)

density

0.788 g/mL at 25 °C (lit.)

SMILES string

CCC1CCCCC1

InChI

1S/C8H16/c1-2-8-6-4-3-5-7-8/h8H,2-7H2,1H3

InChI key

IIEWJVIFRVWJOD-UHFFFAOYSA-N

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Application

Ethylcyclohexane can be used as:
  • A model for alkyl-substituted cycloalkanes to study their rate coefficients of reaction with OH radicals and Cl atoms.
  • A model for light hydrocarbons to investigate their catalytic cracking performance.
  • An organic monomer precursor to synthesize organic-inorganic hybrid polymer thin films by plasma enhanced chemical vapor deposition.

Signal Word

Danger

Hazard Statements

H225,H304,H336,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 2 - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

64.4 °F - closed cup

Flash Point(C)

18 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBS1856
SHBQ3496
05708CX
15105AE
09729LC

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Gas-phase rate coefficients for a series of alkyl cyclohexanes with OH radicals and Cl atoms.
Bejan IG, et al.
International Journal of Chemical Kinetics (2018)
A Fuangswasdi et al.
Water research, 41(6), 1343-1349 (2007-02-03)
Mixtures of anionic and cationic surfactants exhibit synergistic behavior as evidenced by low critical micelle concentrations (CMC) of the mixed system, increased surface activity, and improved detergency performance. The adsorption of a single-head anionic surfactant, sodium dodecyl sulfate (SDS), in
Andrea Mandanici et al.
The Journal of chemical physics, 128(12), 124505-124505 (2008-04-02)
The dynamics of ethylcyclohexane are investigated by high resolution dielectric spectroscopy aiming to characterize the relevant relaxational features of this simple system in its fluid, supercooled liquid, and glassy states. The dielectric signature of structural relaxation is a primary loss
The characteristics of organic-inorganic hybrid low-k thin films by PECVD.
Cho SJ, et al.
Surface and Coatings Technology, 202(22-23), 5654-5658 (2008)
Catalytic cracking of alkylcyclohexanes: Modeling the reaction pathways and mechanisms.
Watson BA, et al.
International Journal of Chemical Kinetics, 29(7), 545-560 (1997)
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