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  • Cyclohexanone is a six-carbon cyclic molecule with a ketone functional group.
  • It is a colorless, oily liquid with an odor reminiscent of oil of peppermint and acetone.
  • Cyclohexanone is slightly soluble in water (5-10 g/100 ml), but miscible with the most common organic solvents.


  • A new organic single crystal of semicarbazone of cyclohexanone (SCCH) has been synthesized and grown as a bulk single crystal by low temperature solution growth technique.
  • Semicarbazone of cyclohexanone was synthesized from the starting materials of semicarbazide hydrochloride and cyclohexanone using sodium acetate as a catalyst.
  • Oxidation of Cyclohexanone to Adipic Acid by a Non-HNO3 route over Co/Mn Cluster Complexes.


  • Cyclohexanone is employed as an industrial solvent and as activator in oxidation reactions.
  • Cyclohexanone is used in the production of adipic acid, cyclohexanone resins, caprolactam and nylon 6.
  • Adipic acid was synthesized from cyclohexanone and concentrated nitric acid.
  • Application of Coincidence Doppler Broadening Spectroscopy to Hydrocarbons at Different Substance States.


  • Technetium, ruthenium, and other nuclides are subsequently separated by solvent extraction with cyclohexanone.
  • The cyclohexylidene derivative of ascorbic acid is freely soluble in light petroleum and water, and insoluble in n-heptane and methyleyelohexane.
  • Cyclohexanone oxime was selected for study because of the potential for human exposure and the interest in oximes as a chemical class.
  • Toxicity studies of cyclohexanone oxime were carried out in male and female B6C3F 1 mice.

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