Harman Patil (Editor)

Cyclohexanone

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Appearance
  
Colorless liquid

Formula
  
C6H10O

Boiling point
  
155.6 °C

Melting point
  
-16.4 °C

Related compounds
  
Cyclohexanol

Density
  
948 kg/m³

Molar mass
  
98.15 g/mol

Soluble in
  
Water

Cyclohexanone Cyclohexanone Wikipedia

Cyclohexanone is the organic compound with the formula (CH2)5CO. The molecule consists of six-carbon cyclic molecule with a ketone functional group. This colorless oil has an odor reminiscent of peardrop sweets as well as acetone. Over time, samples assume a yellow color due to oxidation. Cyclohexanone is slightly soluble in water and miscible with common organic solvents. Billions of kilograms are produced annually, mainly as a precursor to nylon.

Contents

Cyclohexanone wwwsigmaaldrichcomcontentdamsigmaaldrichstr

Cyclohexanone


Production

Cyclohexanone is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts:

C6H12 + O2 → (CH2)5CO + H2O
Cyclohexanone Cyclohexanone Manufacturers Suppliers amp Exporters

This process co-forms cyclohexanol, and this mixture, called "KA Oil" for ketone-alcohol oil, is the main feedstock for the production of adipic acid. The oxidation involves radicals and the intermediacy of the hydroperoxide C6H11O2H. In some cases, purified cyclohexanol, obtained by hydration of cyclohexene, is the precursor. Alternatively, cyclohexanone can be produced by the partial hydrogenation of phenol:

C6H5OH + 2 H2 → (CH2)5CO

This process can also be adjusted to favor the formation of cyclohexanol.

Laboratory methods

Cyclohexanone CYCLOHEXANONE C6H10O PubChem

Cyclohexanone can be prepared from cyclohexanol by oxidation with chromium trioxide (Jones oxidation). An alternative method utilizes the safer and more readily available oxidant sodium hypochlorite.

Uses

Cyclohexanone Cyclohexanone C6H10O ChemSpider

The great majority of cyclohexanone is consumed in the production of precursors to Nylon 6,6 and Nylon 6. About half of the world's supply is converted to adipic acid, one of two precursors for nylon 6,6. For this application, the KA oil (see above) is oxidized with nitric acid. The other half of the cyclohexanone supply is converted to cyclohexanone oxime. In the presence of sulfuric acid catalyst, the oxime rearranges to caprolactam, a precursor to nylon 6:

Safety

Cyclohexanone CYCLOHEXANONE C6H10O PubChem

Like cyclohexanol, cyclohexanone is not carcinogenic and is only moderately toxic, with a TLV of 25 ppm for the vapor. It is an irritant.

A recent study of plastic tubing used in medical procedures that circulate blood outside the body suggests a link between this compound and decreased heart function, swelling, loss of taste and short term memory loss.

References

Cyclohexanone Wikipedia