Date published: 2026-2-7

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3-tert-Butylphenol (CAS 585-34-2)

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CAS Number:
585-34-2
Molecular Weight:
150.22
Molecular Formula:
C10H14O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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3-tert-Butylphenol is a compound that functions as a stabilizer and antioxidant in various chemical processes. It acts by inhibiting the oxidation of other substances, thereby preventing degradation and maintaining the stability of the system. At the molecular level, 3-tert-Butylphenol interacts with free radicals and reactive oxygen species, neutralizing their harmful effects and preserving the integrity of the reaction environment. 3-Tert-Butylphenol′s mechanism of action involves the donation of hydrogen atoms to reactive species, effectively terminating chain reactions and minimizing the formation of undesirable by-products. In this way, 3-tert-Butylphenol plays a role in maintaining the quality and consistency of chemical processes by protecting against oxidative damage and degradation.


3-tert-Butylphenol (CAS 585-34-2) References

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  2. Simultaneous measurement of urinary bisphenol A and alkylphenols by automated solid-phase extractive derivatization gas chromatography/mass spectrometry.  |  Kuklenyik, Z., et al. 2003. Anal Chem. 75: 6820-5. PMID: 14670041
  3. Aquatic toxicity of four alkylphenols (3-tert-butylphenol, 2-isopropylphenol, 3-isopropylphenol, and 4-isopropylphenol) and their binary mixtures to microbes, invertebrates, and fish.  |  Choi, K., et al. 2004. Environ Toxicol. 19: 45-50. PMID: 14758593
  4. Determination of antioxidants in new and used lubricant oils by headspace-programmed temperature vaporization-gas chromatography-mass spectrometry.  |  del Nogal Sánchez, M., et al. 2010. Anal Bioanal Chem. 398: 3215-24. PMID: 20938768
  5. Polymeric ionic liquid modified organic-silica hybrid monolithic column for capillary electrochromatography.  |  Han, H., et al. 2012. J Chromatogr A. 1246: 9-14. PMID: 22204936
  6. Divergent Reaction Pathways for Phenol Arylation by Arynes: Synthesis of Helicenes and 2-Arylphenols.  |  Truong, T. and Daugulis, O. 2013. Chem Sci. 4: 531-535. PMID: 24077102
  7. Tyrosinase and catechol oxidase activity of copper(I) complexes supported by imidazole-based ligands: structure-reactivity correlations.  |  Wendt, F., et al. 2016. J Biol Inorg Chem. 21: 777-92. PMID: 27333775
  8. Determination of terpin hydrate by gas-liquid chromatography.  |  Kubiak, EJ. 1968. J Pharm Sci. 57: 473-5. PMID: 5655590

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3-tert-Butylphenol, 1 g

sc-256563
1 g
$29.00