Cyclohexanol and Cyclohexanone

doi:10.1002/0471238961.0325031206091908.A01

Paper

Cyclohexanol and Cyclohexanone

Published Dec 4, 2000 · W. B. Fisher, Jan F. VanPeppen

UNKNOWN SJR score

30

Citations

1

Influential Citations

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Abstract

Cyclohexanol is a colorless, viscous liquid with a camphoraceous odor. It is used chiefly as a chemical intermediate, a stabilizer, and a homogenizer for various soap and detergent emulsions, and as a solvent for lacquers and varnishes. Cyclohexanone is a colorless, mobile liquid with an odor suggestive of peppermint and acetone. It is used chiefly as a chemical intermediate and as a solvent for resins, lacquers, dyes, and insecticides. Both cyclohexanol and cyclohexanone are produced commercially by the catalytic oxidation of cyclohexane or the catalytic hydrogenation of phenol. Information presented includes physical properties; manufacture; reactions, derivatives, and uses; economic aspects; specifications and analysis; and health and safety factors. Keywords: Cyclohexanol; Cyclohexanone; Nylon-6; Methylcyclohexanol; Dye solvent

Study Snapshot

Cyclohexanol is used as a chemical intermediate and solvent for resins, lacquers, dyes, and insecticides, while cyclohexanone is used as a solvent for resins, lacquers, dyes, and insecticides.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Paper

Cyclohexanol and Cyclohexanone

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References

Studies on the effects of orally administered dicyclohexyl phthalate in the rat.

DCHP is a weak drug-type inducer of hepatic xenobiotic metabolism in rats, with its hepatic effects different from those of di-(2-ethylhexyl) phthalate.

Citations

Study of Co-operative Dynamics in Cyclohexanol-Xylene Solutions using Dielectric Relaxation Spectroscopy

Cooperative dynamics in cyclohexanol-xylene solutions are influenced by bond braking, bond formation, and selfassociation among molecules, with theoretical results generally aligning with experimental results.

Toward Kilogram-Scale Peroxygenase-Catalyzed Oxyfunctionalization of Cyclohexane

Unspecific peroxygenase from Agrocybe aegerita and H2O2 can produce cyclohexanol/cyclohexanone at kilogram-scale, with potential for future improvements and implementation.

Synthesis, Spectral Studies of Some New Chalcone and Schiff Base Derivatives Derived from Cyclohexanone and Molecular Docking and Biological Activity Studies

New cyclohexanone derivatives synthesized and characterized show potential as antibacterial and antifungal agents in medical chemistry.

Converting Cyclohexanone to Liquid Fuel-Grade Products: A Characterization and Comparison Study of Hydrotreating Molybdenum Catalysts

Molybdenum-based hydrotreating catalysts efficiently convert cyclohexanone to liquid bio-fuels, with heating values enhanced by up to 22.7%.

Quantitative analysis of liquid-phase adsorption over chromium-containing metal–organic frameworks of MTN topology

Adsorption of cyclohexanone, cyclohexanol, and tert-butanol over Cr-MIL-100 and Cr-MIL-101 metal-organic frameworks shows two types of adsorption centers, with chromium atoms playing a

Liquid–liquid equilibrium of ternary systems containing cyclohexene, cyclohexanone, water, dimethyl sulfoxide

Experimental and calculated data for liquid-liquid equilibrium in ternary systems containing cyclohexene, cyclohexanone, water, and dimethyl sulfoxide are in good agreement.

Iron Triflate Salts as Highly Active Catalysts for the Solvent‐Free Oxidation of Cyclohexane

Iron triflates show high activity for the solvent-free oxidation of cyclohexane into cyclohexanol and cyclohexanone, with initial turnover frequencies of over 10,000 h-1.