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1-tert-Butyl-3,5-dimethylbenzene (CAS 98-19-1)

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Alternate Names:
5-tert-Butyl-m-xylene
CAS Number:
98-19-1
Molecular Weight:
162.27
Molecular Formula:
C1218
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1-tert-Butyl-3,5-dimethylbenzene functions as a solvent in various experimental applications. It is known for its ability to dissolve other substances, making it useful for the extraction and purification of organic compounds in research and development applications. 1-Tert-Butyl-3,5-Dimethylbenzene interacts at the molecular level, forming non-covalent interactions with other molecules to facilitate the separation and isolation of specific compounds. Its mechanism of action involves disrupting intermolecular forces between different substances, allowing for the extraction of desired compounds from complex mixtures. In experimental applications, 1-tert-Butyl-3,5-dimethylbenzene plays a functional role in enabling the isolation and purification of organic compounds, contributing to the progress of various research endeavors.


1-tert-Butyl-3,5-dimethylbenzene (CAS 98-19-1) References

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  2. Toluene combustion: reaction paths, thermochemical properties, and kinetic analysis for the methylphenyl radical + O2 reaction.  |  da Silva, G., et al. 2007. J Phys Chem A. 111: 8663-76. PMID: 17696501
  3. Aromatic hydroxylation at a non-heme iron center: observed intermediates and insights into the nature of the active species.  |  Makhlynets, OV. and Rybak-Akimova, EV. 2010. Chemistry. 16: 13995-4006. PMID: 21117047
  4. Discovery of 4-tert-butyl-2,6-dimethylphenylsulfur trifluoride as a deoxofluorinating agent with high thermal stability as well as unusual resistance to aqueous hydrolysis, and its diverse fluorination capabilities including deoxofluoro-arylsulfinylation with high stereoselectivity.  |  Umemoto, T., et al. 2010. J Am Chem Soc. 132: 18199-205. PMID: 21125999
  5. Direct arylation of oligonaphthalenes using PIFA/BF3·Et2O: from double arylation to larger oligoarene products.  |  Guo, W., et al. 2013. J Org Chem. 78: 8169-75. PMID: 23859634
  6. Resonance Energy of an Arene Hydrocarbon from Heat of Combustion Measurements.  |  Kolesnichenko, VL. 2015. J Chem Educ. 92: 2170-2172. PMID: 26997668
  7. Cross-Dehydrogenative-Coupling of Alkoxybenzenes with Toluenes: Copper(II) Halide Mediated Tandem Halo/Benzylation of Arenes.  |  Storr, TE., et al. 2016. Chemistry. 22: 18169-18178. PMID: 27935204
  8. Porous Organic Materials: Strategic Design and Structure-Function Correlation.  |  Das, S., et al. 2017. Chem Rev. 117: 1515-1563. PMID: 28035812
  9. Nanoengineering Triplet-Triplet Annihilation Upconversion: From Materials to Real-World Applications.  |  Schloemer, T., et al. 2023. ACS Nano. 17: 3259-3288. PMID: 36800310

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-tert-Butyl-3,5-dimethylbenzene, 100 g

sc-237627
100 g
$56.00