Date published: 2025-10-20

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4-Phenylbenzophenone (CAS 2128-93-0)

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Alternate Names:
4-Benzoylbiphenyl; (Biphenyl-4-yl)(phenyl)methanone
CAS Number:
2128-93-0
Molecular Weight:
258.3
Molecular Formula:
C19H14O
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-Phenylbenzophenone is utilized in the scientific community as a building block for the synthesis of diverse organic compounds, including agrochemicals. Furthermore, it serves as an intermediate in the production of dyes, plastics, and various materials. The significance of 4-Phenylbenzophenone extends to its examination within the realm of biochemistry and physiology. It is hypothesized that this compound interacts with specific receptors in the body, initiating a cascade of biochemical and physiological responses. This receptor binding event is believed to activate various pathways, ultimately leading to the desired effects.


4-Phenylbenzophenone (CAS 2128-93-0) References

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  3. Structural basis for the improved potency of peroxisome proliferator-activated receptor (PPAR) agonists.  |  Peng, YH., et al. 2010. ChemMedChem. 5: 1707-16. PMID: 20734309
  4. ULTRA: A Unique Instrument for Time-Resolved Spectroscopy.  |  Greetham, GM., et al. 2010. Appl Spectrosc. 64: 1311-9. PMID: 21144146
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  6. Survey on the occurrence of photo-initiators and amine synergists in cartonboard packaging on the German market and their migration into the packaged foodstuffs.  |  Jung, T., et al. 2013. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 30: 1993-2016. PMID: 24107105
  7. Evaluation of the migration of 15 photo-initiators from cardboard packaging into Tenax(®) using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS).  |  Van Den Houwe, K., et al. 2014. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 31: 767-75. PMID: 24447245
  8. Electrochemical reduction of aromatic ketones in 1-butyl-3-methylimidazolium-based ionic liquids in the presence of carbon dioxide: the influence of the ketone substituent and the ionic liquid anion on bulk electrolysis product distribution.  |  Zhao, SF., et al. 2015. Phys Chem Chem Phys. 17: 19247-54. PMID: 26136079
  9. Photophysical properties of hexyl diethylaminohydroxybenzoylbenzoate (Uvinul A Plus), a UV-A absorber.  |  Shamoto, Y., et al. 2017. Photochem Photobiol Sci. 16: 1449-1457. PMID: 28782789
  10. Target and suspect screening of substances liable to migrate from food contact paper and cardboard materials using liquid chromatography-high resolution tandem mass spectrometry.  |  Blanco-Zubiaguirre, L., et al. 2020. Talanta. 208: 120394. PMID: 31816794
  11. Synthesis of Aryldiphenylphosphine Oxides by Quaternization of Tertiary Diphenylphosphines with Aryl Bromides Followed by the Wittig Reaction.  |  Zhong, CH. and Huang, W. 2020. ACS Omega. 5: 16010-16020. PMID: 32656422
  12. In vitro and computational studies of the antioxidant and anti-diabetic properties of Bridelia ferruginea.  |  Oyebode, O., et al. 2022. J Biomol Struct Dyn. 40: 3989-4003. PMID: 33272106
  13. Cumulative Dietary Risk Assessment of Benzophenone-Type Photoinitiators from Packaged Foodstuffs.  |  Chen, ML., et al. 2022. Foods. 11: PMID: 35053884

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Phenylbenzophenone, 50 g

sc-262133
50 g
$78.00