Date published: 2025-9-5

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1-Hexanol (CAS 111-27-3)

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Alternate Names:
n-Hexyl alcohol
CAS Number:
111-27-3
Purity:
≥98%
Molecular Weight:
102.17
Molecular Formula:
C6H14O
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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1-Hexanol is an organic compound that is part of the alcohol family with a six-carbon chain, making it a higher alcohol compared to its more common and simpler counterparts like methanol and ethanol. Characterized by the presence of a hydroxyl group attached to its first carbon atom, 1-hexanol is notable for its relatively high molecular weight which imparts unique physical and chemical properties such as a higher boiling point and greater viscosity compared to lower alcohols. In research, 1-hexanol has been extensively utilized as a non-polar solvent due to its ability to dissolve substances that do not readily dissolve in water, making it invaluable in the study of hydrophobic compounds. Furthermore, this alcohol plays a critical role in the study of biological membrane processes and the behavior of lipids due to its interaction with lipid bilayers, where it is used to alter membrane fluidity and permeability in controlled experimental setups. In the field of green chemistry, 1-hexanol is also studied for its potential as a biofuel component because of its renewable origins and favorable combustion properties. Its role in organic synthesis is significant as well; it serves as a starting material or intermediate in the manufacture of perfumes, plasticizers, and other organic compounds, thereby facilitating a deeper understanding of complex synthetic pathways and reaction mechanisms.


1-Hexanol (CAS 111-27-3) References

  1. Modulation of actomyosin motor function by 1-hexanol.  |  Komatsu, H., et al. 2004. J Muscle Res Cell Motil. 25: 77-85. PMID: 15160491
  2. The inhibition of N2O5 hydrolysis in sulfuric acid by 1-butanol and 1-hexanol surfactant coatings.  |  Park, SC., et al. 2007. J Phys Chem A. 111: 2921-9. PMID: 17388402
  3. Solubility of lovastatin in a family of six alcohols: Ethanol, 1-propanol, 1-butanol, 1-pentanol, 1-hexanol, and 1-octanol.  |  Nti-Gyabaah, J., et al. 2008. Int J Pharm. 359: 111-7. PMID: 18490118
  4. Effects of 1-hexanol on C12E10 micelles: a molecular simulations and light scattering study.  |  Vierros, S. and Sammalkorpi, M. 2018. Phys Chem Chem Phys. 20: 6287-6298. PMID: 29431748
  5. Mutual and Thermal Diffusivities as well as Fluid-Phase Equilibria of Mixtures of 1-Hexanol and Carbon Dioxide.  |  Wu, W., et al. 2020. J Phys Chem B. 124: 2482-2494. PMID: 32105484
  6. Sex Pheromone of the Alfalfa Plant Bug, Adelphocoris lineolatus: Pheromone Composition and Antagonistic Effect of 1-Hexanol (Hemiptera: Miridae).  |  Koczor, S., et al. 2021. J Chem Ecol. 47: 525-533. PMID: 33871786
  7. Crystallization Thermodynamics of α-Lactose Monohydrate in Different Solvents.  |  Guan, Y., et al. 2022. Pharmaceutics. 14: PMID: 36145520
  8. Antibacterial Activity of Hexanol Vapor In Vitro and on the Surface of Vegetables.  |  Kyoui, D., et al. 2023. Foods. 12: PMID: 37628096
  9. The nature of uncoupling by n-hexane, 1-hexanethiol and 1-hexanol in rat liver mitochondria.  |  Canton, M., et al. 1996. Biochim Biophys Acta. 1274: 39-47. PMID: 8645693

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Hexanol, 5 ml

sc-213334
5 ml
$20.00

1-Hexanol, 100 ml

sc-213334A
100 ml
$26.00