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.
Organic synthesis.
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.
ChEBI: Ethylcyclohexane is a cycloalkane.
Ethylcyclohexane may be incompatible with strong oxidizing agents such as nitric acid. Charring may occur followed by ignition of unreacted hydrocarbon and other nearby combustibles. In other settings mostly unreactive. Not affected by aqueous solutions of acids, alkalis, most oxidizing agents, and most reducing agents. When heated sufficiently or when ignited in the presence of air, oxygen or strong oxidizing agents, burns exothermically to produce carbon dioxide and water.
Flammable, moderate fire risk; flammable
limits in air 0.9–6.6%.
Diziness, with nausea and vomiting. Concentrated vapor may cause collapse and unconsciousness.
Flammability and Explosibility
Not classified
Ethylcyclohexane [1678-91-7] M 112.2, b 131.2o/742mm, d 4 0.7839, n D 1.43304, n D 1.43073. Purify it by azeotropic distillation with 2-ethoxyethanol; then the alcohol is washed out with water and, after drying, the ethylcyclohexane is redistilled. The dried material has been repeatedly fractionated over Na. [Baker & Groves J Chem Soc 1148 1939, Beilstein 5 H 35, 5 III 90, 5 IV 115.]
