Date published: 2025-10-7

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Cyclohexanol (CAS 108-93-0)

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Alternate Names:
cyclohexyl alcohol
Application:
Cyclohexanol is used as a precursor to nylons and plasticizers
CAS Number:
108-93-0
Purity:
≥98%
Molecular Weight:
100.16
Molecular Formula:
C6H12O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cyclohexanol is a chemical compound that functions as a solvent in various experiments. It is known for its ability to dissolve a wide range of organic and inorganic substances, making it useful for extraction and purification processes in development. At the molecular level, cyclohexanol interacts with other compounds through hydrogen bonding and van der Waals forces, allowing it to effectively solvate and disperse different types of molecules. The mode of action involves disrupting intermolecular forces and facilitating the dissolution of solutes, which is for various experimental procedures. Cyclohexanol can participate in chemical reactions as a reactant or catalyst, contributing to the synthesis of new compounds in laboratory applications. Its versatile nature and ability to interact with different substances make it a component in experimental processes, where its solvent properties play a role in various chemical and biochemical studies.


Cyclohexanol (CAS 108-93-0) References

  1. Co-carcinogenic effect of cyclohexanol on the development of preneoplastic lesions in a rat hepatocarcinogenesis model.  |  Márquez-Rosado, L., et al. 2007. Mol Carcinog. 46: 524-33. PMID: 17393424
  2. Polymorphism in cyclohexanol.  |  Ibberson, RM., et al. 2008. Acta Crystallogr B. 64: 573-82. PMID: 18799845
  3. Cyclohexanol analogues are positive modulators of GABA(A) receptor currents and act as general anaesthetics in vivo.  |  Hall, AC., et al. 2011. Eur J Pharmacol. 667: 175-81. PMID: 21658385
  4. Optimization of Cyclohexanol and Cyclohexanone Yield in the Photocatalytic Oxofunctionalization of Cyclohexane over Degussa P-25 under Visible Light.  |  Henríquez, A., et al. 2019. Molecules. 24: PMID: 31208090
  5. Anaerobic metabolism of cyclohexanol by denitrifying bacteria.  |  Dangel, W., et al. 1988. Arch Microbiol. 150: 358-62. PMID: 3202667
  6. Insights into protonation for cyclohexanol/water mixtures at the zeolitic Brønsted acid site.  |  Liu, P., et al. 2021. Phys Chem Chem Phys. 23: 10395-10401. PMID: 33889887
  7. Antagonistic postsynaptic and presynaptic actions of cyclohexanol on neuromuscular synaptic transmission and function.  |  Dissanayake, KN., et al. 2021. J Physiol. 599: 5417-5449. PMID: 34748643
  8. Recent progress on selective hydrogenation of phenol toward cyclohexanone or cyclohexanol.  |  Xue, G., et al. 2021. Nanotechnology. 33: PMID: 34757948
  9. Adsorptive separation of cyclohexanol and cyclohexanone by nonporous adaptive crystals of RhombicArene.  |  Zhao, Y., et al. 2021. Chem Sci. 12: 15528-15532. PMID: 35003581
  10. Cobalt-Graphene Catalyst for Selective Hydrodeoxygenation of Guaiacol to Cyclohexanol.  |  Guo, Q., et al. 2022. Nanomaterials (Basel). 12: PMID: 36234516
  11. Electrifying Adipic Acid Production: Copper-Promoted Oxidation and C-C Cleavage of Cyclohexanol.  |  Wang, R., et al. 2022. Angew Chem Int Ed Engl. 61: e202214977. PMID: 36261886
  12. Selective Oxidation of Cyclohexane to Cyclohexanol/Cyclohexanone by Surface Peroxo Species on Cu-Mesoporous TiO2.  |  Shan, YD., et al. 2023. Inorg Chem. 62: 4872-4882. PMID: 36916853
  13. Phenol Hydrogenation to Cyclohexanol Catalysed by Palladium Supported on CuO/CeO2.  |  Kasabe, MM., et al. 2023. Chem Asian J. 18: e202300119. PMID: 37092683

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cyclohexanol, 25 ml

sc-214785
25 ml
$27.00

Cyclohexanol, 1 L

sc-214785A
1 L
$44.00