Date published: 2025-10-16

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Cyclohexanone (CAS 108-94-1)

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CAS Number:
108-94-1
Molecular Weight:
98.14
Molecular Formula:
C6H10O
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cyclohexanone, an organic compound with the molecular formula C6H10O, presents itself as a colorless oily liquid with a distinctive odor. This versatile substance serves as a valuable reagent in organic synthesis. With its six-membered ring structure, it falls into the category of cyclic ketones, belonging to the cycloalkanone family. Its widespread industrial application involves being a common component in the production of nylon, plasticizers, and certain pharmaceuticals. Furthermore, it finds utility as a solvent in laboratory experiments. Its significance extends to various scientific research areas, where it plays a pivotal role in the synthesis of diverse compounds, such as pharmaceuticals, dyes, and fragrances. Moreover, it contributes to the creation of polymers and other materials, including cyclic compounds like cyclic peptides and cyclic nucleotides. This substance is thought to function as an electron donor, providing electrons to a molecule to facilitate the creation of a new bond. Additionally, it is believed to act as an electron acceptor, receiving electrons from a molecule to enable the formation of another new bond.


Cyclohexanone (CAS 108-94-1) References

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  2. Mechanistic studies of cyclohexanone monooxygenase: chemical properties of intermediates involved in catalysis.  |  Sheng, D., et al. 2001. Biochemistry. 40: 11156-67. PMID: 11551214
  3. Monitoring of exposure to cyclohexanone through the analysis of breath and urine.  |  Ong, CN., et al. 1991. Scand J Work Environ Health. 17: 430-5. PMID: 1788536
  4. Determination of cyclohexanol in urine and its use in environmental monitoring of cyclohexanone exposure.  |  Ong, CN., et al. 1991. J Anal Toxicol. 15: 13-6. PMID: 2046335
  5. Robust cyclohexanone selective chemiresistors based on single-walled carbon nanotubes.  |  Frazier, KM. and Swager, TM. 2013. Anal Chem. 85: 7154-8. PMID: 23886453
  6. Isomerization and Fragmentation of Cyclohexanone in a Heated Micro-Reactor.  |  Porterfield, JP., et al. 2015. J Phys Chem A. 119: 12635-47. PMID: 26617252
  7. Assessment of cyclohexanone toxicity in inhalation-exposed F344 rats and B6C3F1 mice: applications in occupational health.  |  Lim, CH., et al. 2018. Inhal Toxicol. 30: 247-254. PMID: 30265164
  8. RIFM fragrance ingredient safety assessment, cyclohexanone, 2-ethyl-4,4-dimethyl-, CAS Registry Number 55739-89-4.  |  Api, AM., et al. 2019. Food Chem Toxicol. 134 Suppl 1: 110604. PMID: 31233868
  9. Optimization of chemoenzymatic Baeyer-Villiger oxidation of cyclohexanone to ε-caprolactone using response surface methodology.  |  Zhang, Y., et al. 2020. Biotechnol Prog. 36: e2901. PMID: 31465150
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  11. Chemoselectivity issues of the asymmetric interaction between cyclohexanone, β-nitrostyrene, and benzoic acid under 5-aryl prolinate's organocatalysis.  |  Ivantcova, PM. and Kudryavtsev, KV. 2020. Chirality. 32: 833-841. PMID: 32168390
  12. Association of Neurodevelopmental Outcomes With Environmental Exposure to Cyclohexanone During Neonatal Congenital Cardiac Operations: A Secondary Analysis of a Randomized Clinical Trial.  |  Everett, AD., et al. 2020. JAMA Netw Open. 3: e204070. PMID: 32374395
  13. Asymmetric Organocatalyzed Intermolecular Functionalization of Cyclohexanone-Derived Dienones.  |  Coutant, C., et al. 2023. Chem Rec. 23: e202300042. PMID: 37058133

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cyclohexanone, 25 ml

sc-214786
25 ml
$31.00

Cyclohexanone, 500 ml

sc-214786A
500 ml
$27.00