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4-Ethylthiophenol (CAS 4946-13-8)

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Alternate Names:
4-Ethylbenzenethiol; 4-Ethylphenyl mercaptan
Application:
4-Ethylthiophenol is a compound used in the study of self-assembled monolayers (SAMs)
CAS Number:
4946-13-8
Molecular Weight:
138.23
Molecular Formula:
C8H10S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4-Ethylthiophenol is a compound used in the study of self-assembled monolayers (SAM). Aromatic thiols are often used as SAMs because sulfur has a high affinity for substrates that are noble metals, such as gold. Some applications of SAMs include surface modification, biosensors, nanotechnology, corrosion protection, molecular electronics, and lubrication. 4-Ethylthiophenol is used to increase cell membrane permeability, study enzyme inhibition, and produce polymers. It is also researched for its potential use as a fuel additive and a corrosion inhibitor.


4-Ethylthiophenol (CAS 4946-13-8) References

  1. The active site of the thermophilic CYP119 from Sulfolobus solfataricus.  |  Koo, LS., et al. 2000. J Biol Chem. 275: 14112-23. PMID: 10799487
  2. The pancreas-specific protein disulphide-isomerase PDIp interacts with a hydroxyaryl group in ligands.  |  Klappa, P., et al. 2001. Biochem J. 354: 553-9. PMID: 11237859
  3. Synthesis and Characterization of Oxotechnetium(V) Mixed-Ligand Complexes Containing a Tridentate N-Substituted Bis(2-mercaptoethyl)amine and a Monodentate Thiol.  |  Pirmettis, IC., et al. 1996. Inorg Chem. 35: 1685-1691. PMID: 11666392
  4. Design, synthesis and in vitro evaluation of novel derivatives as serotonin N-acetyltransferase inhibitors.  |  Beaurain, N., et al. 2002. J Enzyme Inhib Med Chem. 17: 409-14. PMID: 12683677
  5. Identification of estrogen-like alkylphenols in produced water from offshore oil installations.  |  Boitsov, S., et al. 2007. Mar Environ Res. 64: 651-65. PMID: 17714776
  6. Methyl mercapturate synthesis: an efficient, convenient and simple method.  |  Cossec, B., et al. 2008. Molecules. 13: 2394-407. PMID: 18830162
  7. Fabrication of polymer nanocavities with tailored openings.  |  Tan, LH., et al. 2009. ACS Nano. 3: 3469-74. PMID: 19817393
  8. Glutathione pathway in ethylbenzene metabolism: novel biomarkers of exposure in the rat.  |  Cossec, B., et al. 2010. Chemosphere. 81: 1334-41. PMID: 20825968
  9. Quantitative structure-property relationships of retention indices of some sulfur organic compounds using random forest technique as a variable selection and modeling method.  |  Goudarzi, N., et al. 2016. J Sep Sci. 39: 3835-3842. PMID: 27510356
  10. Effect of Thiolated Ligands in Au Nanowire Synthesis.  |  Wang, Y., et al. 2017. Small. 13: PMID: 28857468
  11. A Robust Pd-Catalyzed C-S Cross-Coupling Process Enabled by Ball-Milling.  |  Jones, AC., et al. 2020. Org Lett. 22: 7433-7438. PMID: 32941045
  12. Fluorinated tricyclic neuroleptics with prolonged action: 8-Alkyl derivatives of 3-fluoro-10-piperazino-10,11-dihydrodibenzo[b,f]thiepins  |  Jiří Jílek, Miroslav Rajšner, Jiřina Metyšová, Josef Pomykáček and Miroslav Protiva. 1984. Collect. Czech. Chem. Commun., 49,: 2638-2648.
  13. Synergistic effects for fast co-pyrolysis of strong-acid cation exchange resin and cellulose using Py-GC/MS  |  Jun Zhang a b c d 1, Chengyu Li a b c d e 1, Jing Gu a b c d, Haoran Yuan a b c d, Yong Chen a b c d. 15 October 2021,. Fuel. Volume 302,: 121232.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Ethylthiophenol, 5 g

sc-396709
5 g
$241.00

4-Ethylthiophenol, 25 g

sc-396709A
25 g
$741.00