Date published: 2025-10-14

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2-Ethylphenol (CAS 90-00-6)

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Alternate Names:
o-Ethylphenol
CAS Number:
90-00-6
Molecular Weight:
122.16
Molecular Formula:
C8H10O
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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2-Ethylphenol (2-EP) is an aromatic hydrocarbon compound that carries a distinctive scent. It presents as a colorless, oily liquid, which can dissolve in organic solvents and boasts a boiling point of 191°C. This natural compound occurs in the environment and holds applications in several industrial and commercial realms. It serves as a precursor for synthesizing other compounds, acts as a plasticizer, and contributes to flavors and fragrances. Researchers have taken an interest in exploring the potential impact of 2-Ethylphenol on health and disease. Though the precise mechanism of action remains under investigation, it is believed that 2-Ethylphenol might interact with different receptors and enzymes to modulate their activities. For instance, studies have shown its inhibitory effect on cyclooxygenase-2 (COX-2), an enzyme linked to the synthesis of pro-inflammatory molecules. Additionally, it has been observed to regulate the activity of various proteins responsible for controlling cell division and apoptosis. 2-Ethylphenol is a fascinating compound with diverse applications and potential health benefits. Ongoing research is shedding light on its mechanisms of action and its promising role in addressing certain health conditions.


2-Ethylphenol (CAS 90-00-6) References

  1. Anaerobic biodegradability of alkylphenols and fuel oxygenates in the presence of alternative electron acceptors.  |  Puig-Grajales, L., et al. 2000. Appl Microbiol Biotechnol. 54: 692-7. PMID: 11131397
  2. Toxicity and kinetic parameters of the aerobic biodegradation of the phenol and alkylphenols by a mixed culture.  |  Acuña-Argüelles, ME., et al. 2003. Biotechnol Lett. 25: 559-64. PMID: 12882145
  3. Inhibition of the acetoclastic methanogenic activity by phenol and alkyl phenols.  |  Olguin-Lora, P., et al. 2003. Environ Technol. 24: 999-1006. PMID: 14509391
  4. Metabolic activation of carcinogenic ethylbenzene leads to oxidative DNA damage.  |  Midorikawa, K., et al. 2004. Chem Biol Interact. 150: 271-81. PMID: 15560893
  5. The effect of functional groups on oligomerization of phenolics on activated carbon.  |  Lu, Q. and Sorial, GA. 2007. J Hazard Mater. 148: 436-45. PMID: 17442485
  6. Mechanism of ethylbenzene-induced mouse-specific lung tumor: metabolism of ethylbenzene by rat, mouse, and human liver and lung microsomes.  |  Saghir, SA., et al. 2009. Toxicol Sci. 107: 352-66. PMID: 19075040
  7. Insecticidal properties of phenols on Culex quinquefasciatus Say and Musca domestica L.  |  Pavela, R. 2011. Parasitol Res. 109: 1547-53. PMID: 21523422
  8. Cs(x)H(3.0-x)PW12O40 (X = 2.0-3.0) heteropolyacid nano-catalysts for catalytic decomposition of 2,3-dihydrobenzofuran to aromatics.  |  Kim, JK., et al. 2014. J Nanosci Nanotechnol. 14: 8884-90. PMID: 25958622
  9. Catalytic Decomposition of 2,3-Dihydrobenzofuran to Monocyclic Compounds Over Palladium Catalysts Supported on Sulfonated Ordered Mesoporous Carbon.  |  Kim, JK., et al. 2015. J Nanosci Nanotechnol. 15: 9139-44. PMID: 26726658
  10. Monitoring alkylphenols in water using the polar organic chemical integrative sampler (POCIS): Determining sampling rates via the extraction of PES membranes and Oasis beads.  |  Silvani, L., et al. 2017. Chemosphere. 184: 1362-1371. PMID: 28693101
  11. O-demethylation, dehydroxylation, ring-reduction and cleavage of aromatic substrates by Enterobacteriaceae under anaerobic conditions.  |  Grbić-Galić, D. 1986. J Appl Bacteriol. 61: 491-7. PMID: 3549663
  12. Depolymerization of Rice Straw Lignin into Value-Added Chemicals in Sub-Supercritical Ethanol.  |  Tran, VT., et al. 2022. ScientificWorldJournal. 2022: 7872307. PMID: 35645630
  13. [Synthesis of 4-chloro-2-ethylphenol by chlorination of 2-ethylphenol].  |  Schrötter, E. and Krüger, W. 1974. Pharmazie. 29: 269-73. PMID: 4849861

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Ethylphenol, 5 g

sc-238038
5 g
$22.00

2-Ethylphenol, 25 g

sc-238038A
25 g
$70.00