Date published: 2026-4-4

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Hexylbenzene (CAS 1077-16-3)

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Alternate Names:
1-Phenylhexane
CAS Number:
1077-16-3
Purity:
≥98%
Molecular Weight:
162.27
Molecular Formula:
C12H18
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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Hexylbenzene is a chemical compound that functions as a solvent in various development processes. It acts by dissolving non-polar compounds and facilitating reactions between different substances. At the molecular level, hexylbenzene interacts with other compounds by forming weak intermolecular forces, allowing it to effectively solvate non-polar molecules. This enables to carry out a wide range of experimental procedures, including extraction, chromatography, and synthesis of organic compounds. Hexylbenzene′s mode of action involves its ability to interact with non-polar substances, aiding in the manipulation and separation of different compounds in experimental applications. Its solvent properties make it a useful component in various development applications, where the dissolution and manipulation of non-polar compounds are required.


Hexylbenzene (CAS 1077-16-3) References

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  2. Dependence of selective enclathration on types of cholic acid crystals.  |  Yoswathananont, N., et al. 2003. Org Biomol Chem. 1: 210-4. PMID: 12929413
  3. On-line concentration of neutral and charged species in capillary electrochromatography with a methacrylate-based monolithic stationary phase.  |  Ping, G., et al. 2004. Electrophoresis. 25: 421-7. PMID: 14760633
  4. Light-sensitive microemulsions.  |  Eastoe, J., et al. 2004. Langmuir. 20: 1120-5. PMID: 15803685
  5. Shape-persistent macrocycle with a self-complementary recognition pattern based on diacetylene-linked alternating hexylbenzene and perfluorobenzene rings.  |  Shu, L. and Mayor, M. 2006. Chem Commun (Camb). 4134-6. PMID: 17024272
  6. Revealing the way of self-complementary dimerization for a shape-persistent macrocycle using density functional theory calculations.  |  Ng, MF. and Yang, SW. 2007. J Phys Chem B. 111: 13886-93. PMID: 18044867
  7. Solubilization of n-alkylbenzenes into decanoyl-N-methylglucamide (Mega-10) solution.  |  Nakamura, S., et al. 2008. Langmuir. 24: 15-8. PMID: 18052401
  8. Solubilization of n-alkylbenzenes into decanoyl-N-methylglucamide (Mega-10) solution; temperature dependence.  |  Nakamura, S., et al. 2009. Colloids Surf B Biointerfaces. 69: 135-40. PMID: 19150232
  9. Olfactory detectability of homologous n-alkylbenzenes as reflected by concentration-detection functions in humans.  |  Cometto-Muñiz, JE. and Abraham, MH. 2009. Neuroscience. 161: 236-48. PMID: 19303922
  10. The performance of hybrid monolithic silica capillary columns prepared by changing feed ratios of tetramethoxysilane and methyltrimethoxysilane.  |  Hara, T., et al. 2010. J Chromatogr A. 1217: 89-98. PMID: 19945709
  11. The effect of hydrothermal treatment on column performance for monolithic silica capillary columns.  |  Hara, T., et al. 2011. J Chromatogr A. 1218: 3624-35. PMID: 21546027
  12. Combinations of Aromatic and Aliphatic Radiolysis.  |  LaVerne, JA. and Dowling-Medley, J. 2015. J Phys Chem A. 119: 10125-9. PMID: 26387844
  13. Effect of polyethylene glycol on pore structure and separation efficiency of silica-based monolithic capillary columns.  |  Hara, T., et al. 2016. J Chromatogr A. 1442: 42-52. PMID: 26976349
  14. Kinetics of Intramolecular Phenyl Migration and Fused Ring Formation in Hexylbenzene Radicals.  |  Khanniche, S., et al. 2018. J Phys Chem A. 122: 9778-9791. PMID: 30485093
  15. De Novo Prediction of Binders and Nonbinders for T4 Lysozyme by gREST Simulations.  |  Niitsu, A., et al. 2019. J Chem Inf Model. 59: 3879-3888. PMID: 31390205

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Hexylbenzene, 1 ml

sc-250113
1 ml
$42.00