Date published: 2025-11-17

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2,3-Dimethylphenol (CAS 526-75-0)

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Alternate Names:
3-Hydroxyl-o-xylene
CAS Number:
526-75-0
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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2,3-Dimethylphenol is a chemical compound that functions as a substrate in various chemical reactions, particularly in the synthesis of polymers. It acts as a precursor in the production of antioxidants, flame retardants, and other specialty chemicals. At the molecular level, 2,3-Dimethylphenol undergoes specific chemical reactions, such as acylation and alkylation, to form new compounds with desired properties. Its mode of action involves participating in nucleophilic aromatic substitution reactions, leading to the formation of substituted phenolic compounds. 2,3-Dimethylphenol plays a role in the modification of organic molecules, contributing to the development of new materials and compounds with specific characteristics.


2,3-Dimethylphenol (CAS 526-75-0) References

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  2. Procedure for the quantification of rider peaks.  |  Jurt, S., et al. 2001. J Chromatogr A. 929: 165-8. PMID: 11594398
  3. Vibrational analysis of substituted phenols: part II. Transferability of valence force constants.  |  Venkata Ramana Rao, P. and Ramana Rao, G. 2002. Spectrochim Acta A Mol Biomol Spectrosc. 58: 3205-21. PMID: 12511105
  4. Determination of phenolic compounds in wastewater by liquid-phase microextraction coupled with gas chromatography.  |  Zhang, T., et al. 2006. J Chromatogr Sci. 44: 619-24. PMID: 17254372
  5. Alkylphenols in the defensive secretion of the nearctic opilionid,Stygnomma spinifera (Arachnida: Opiliones).  |  Duffield, RM., et al. 1981. J Chem Ecol. 7: 445-52. PMID: 24420490
  6. Nanocage structure derived from sulfonated β-cyclodextrin intercalated layered double hydroxides and selective adsorption for phenol compounds.  |  Xue, X., et al. 2014. Inorg Chem. 53: 1521-9. PMID: 24422491
  7. Multi-substrate biodegradation interaction of 1, 4-dioxane and BTEX mixtures by Acinetobacter baumannii DD1.  |  Zhou, Y., et al. 2016. Biodegradation. 27: 37-46. PMID: 26749222
  8. Design of Ultrasensitive Protein Biosensor Strips for Selective Detection of Aromatic Contaminants in Environmental Wastewater.  |  Ray, S., et al. 2018. Anal Chem. 90: 8960-8968. PMID: 30004219
  9. Chlorination of Phenols Revisited: Unexpected Formation of α,β-Unsaturated C4-Dicarbonyl Ring Cleavage Products.  |  Prasse, C., et al. 2020. Environ Sci Technol. 54: 826-834. PMID: 31904937
  10. A highly expressed odorant receptor from the yellow fever mosquito, AaegOR11, responds to (+)- and (-)-fenchone and a phenolic repellent.  |  Lu, W., et al. 2022. Insect Biochem Mol Biol. 151: 103866. PMID: 36347453
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  12. Inhibitors of the Oncogenic PA2G4-MYCN Protein-Protein Interface.  |  Massudi, H., et al. 2023. Cancers (Basel). 15: PMID: 36980710
  13. Cloning of the genes for and characterization of the early stages of toluene and o-xylene catabolism in Pseudomonas stutzeri OX1.  |  Bertoni, G., et al. 1996. Appl Environ Microbiol. 62: 3704-11. PMID: 8837426

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,3-Dimethylphenol, 1 g

sc-238288
1 g
$23.00