Date published: 2025-9-27

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Methylcyclohexane (CAS 108-87-2)

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Alternate Names:
Hexahydrotoluene
Application:
Methylcyclohexane is a methylated cyclohexane compound
CAS Number:
108-87-2
Purity:
≥99%
Molecular Weight:
98.19
Molecular Formula:
C6H11CH3
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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Methylcyclohexane is a saturated hydrocarbon with the chemical formula C7H14, consisting of a cyclohexane ring substituted with a single methyl group. This structure makes it a relatively simple alicyclic compound, which is a colorless, flammable liquid with a subtle, distinctive odor. Methylcyclohexane is primarily used as a solvent in the chemical industry due to its ability to dissolve a variety of organic substances, and it is also employed as a starting material in the synthesis of more complex chemical compounds. In research, methylcyclohexane is frequently utilized in studies related to hydrocarbon behavior in different conditions, especially its phase behavior with other hydrocarbons which is crucial for the petroleum industry. Its thermodynamic properties, like heat capacity and vapor pressure, are often subjects of study to enhance the efficiency of processes where heat transfer is involved, such as in distillation columns and heat exchangers. Additionally, methylcyclohexane is used in materials science research, particularly in the study of non-polar solvent systems, where its interactions with polymers and other organic materials are examined to determine solubility characteristics and reaction kinetics. Moreover, its transformation under various conditions, such as in hydrogenation reactions where it can be converted into more useful derivatives like methylcyclohexanol, is of significant interest. This compound also serves as a model in computational chemistry for studying the dynamics of molecular structures and reaction mechanisms, providing insights into the stability and reactivity of cyclic hydrocarbons.


Methylcyclohexane (CAS 108-87-2) References

  1. The role of hyperconjugation in the conformational analysis of methylcyclohexane and methylheterocyclohexanes.  |  Ribeiro, DS. and Rittner, R. 2003. J Org Chem. 68: 6780-7. PMID: 12919048
  2. Toxicity of Methylcyclohexane and Its Effect on the Reproductive System in SD Rats.  |  Kim, HY., et al. 2011. Saf Health Work. 2: 290-300. PMID: 22953213
  3. Synthesis of Concentrated Methylcyclohexane as Hydrogen Carrier through Photoelectrochemical Conversion of Toluene and Water.  |  Kageshima, Y., et al. 2017. ChemSusChem. 10: 659-663. PMID: 27976520
  4. Disposition of Iridium on Ruthenium Nanoparticle Supported on Ketjenblack: Enhancement in Electrocatalytic Activity toward the Electrohydrogenation of Toluene to Methylcyclohexane.  |  Inami, Y., et al. 2020. ACS Omega. 5: 1221-1228. PMID: 31984280
  5. Chemically synthesized hydrogen fuel from reaction of methylcyclohexane over nanoporous heterogeneous catalysts.  |  Chasib, KF. 2022. Environ Technol. 43: 1961-1967. PMID: 33284739
  6. Combustion of methylcyclohexane at elevated temperatures to investigate burning velocity for surrogate fuel development.  |  Kumar, R., et al. 2021. J Hazard Mater. 406: 124627. PMID: 33296761
  7. Promoting effect of Zn in high-loading Zn/Ni-SiO2 catalysts for selective hydrogen evolution from methylcyclohexane.  |  Alekseeva Bykova, MV., et al. 2022. Dalton Trans. 51: 6068-6085. PMID: 35356959
  8. Dehydrogenation of methylcyclohexane over Pt-based catalysts supported on functional granular activated carbon.  |  Ye, HL., et al. 2021. RSC Adv. 11: 29287-29297. PMID: 35479578
  9. Degradation potential and pathways of methylcyclohexane by bacteria derived from Antarctic surface water.  |  Li, Y., et al. 2023. Chemosphere. 329: 138647. PMID: 37037356

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methylcyclohexane, 1 L

sc-250391
1 L
$257.00