Date published: 2025-12-18

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4,4′-Dibromotriphenylamine (CAS 81090-53-1)

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Alternate Names:
N,N-Bis(4-bromophenyl)aniline
Application:
4,4′-Dibromotriphenylamine is a synthetic reagent for proteomics research
CAS Number:
81090-53-1
Molecular Weight:
403.12
Molecular Formula:
C18H13Br2N
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4,4′-Dibromotriphenylamine is a brominated derivative of aniline, a primary aromatic amine. It is a synthetic reagent for proteomics research. It is also employed as a starting material in the synthesis of various compounds. 4,4′-Dibromotriphenylamine acts as an inhibitor of enzymes involved in metabolism, a substrate for certain enzymes, and a modulator of certain receptor systems.


4,4′-Dibromotriphenylamine (CAS 81090-53-1) References

  1. A bipolar transporter as an efficient green fluorescent emitter and host for red phosphors in multi- and single-layer organic light-emitting diodes.  |  Ye, J., et al. 2014. Chemistry. 20: 13762-9. PMID: 25186337
  2. Oxidative Dimerization of Triarylamines Promoted by WCl6, Including the Solid State Isolation and the Crystallographic Characterization of a Triphenylammonium Salt.  |  Bortoluzzi, M., et al. 2016. Inorg Chem. 55: 887-93. PMID: 26701200
  3. Ambient Pressure X-ray Photoelectron Spectroscopy Investigation of Thermally Stable Halide Perovskite Solar Cells via Post-Treatment.  |  Ning, S., et al. 2020. ACS Appl Mater Interfaces. 12: 43705-43713. PMID: 32885658
  4. Development of triarylamine mediator having ionic-tag and its application to electrocatalytic reaction in ionic liquid  |  Takahashi, K., Furusawa, T., Sawamura, T., Kuribayashi, S., Inagi, S., & Fuchigami, T. 2012. Electrochimica acta. 77: 47-53.
  5. AIE active triphenylamine–benzothiazole based motifs: ESIPT or ICT emission  |  Padalkar, V. S., Sakamaki, D., Kuwada, K., Tohnai, N., Akutagawa, T., Sakai, K. I., & Seki, S. 2016. RSC advances. 6(32): 26941-26949.
  6. Triphenylamine Based Random Copolymers: The Effect of Molecular Weight on Performance of Solar Cell and Optoelectronic Properties  |  Goker, S., Hacioglu, S. O., Hizalan, G., Aktas, E., Cirpan, A., & Toppare, L. 2017. Macromolecular Chemistry and Physics. 218(18): 1600544.
  7. Optical, electrochemical, and sensing properties of polyfluorenes bearing thiazole or oxazole and triphenylamine in the main chain  |  Sarigiannis, Y., & Spiliopoulos, I. K. 2017. Journal of Polymer Science Part A: Polymer Chemistry. 55(2): 243-254.
  8. Syntheses, characterizations and luminescence properties of four novel coordination polymers based on 4, 4′-(phenylazanediyl) dibenzoic acid with two rigid N-donor imidazol ligand  |  Zhao, C., Zhao, L., & Zhang, M. 2018. Inorganica Chimica Acta. 469: 136-143.
  9. o, p‐Dimethoxybiphenyl Arylamine Substituted Porphyrins as Hole‐Transport Materials: Electrochemical, Photophysical, and Carrier Mobility Characterization  |  Pudi, R., Rodríguez‐Seco, C., Vidal‐Ferran, A., Ballester, P., & Palomares, E. 2018. European Journal of Organic Chemistry. 2018(18): 2064-2070.
  10. Optical and electrochemical properties and sensing application for iron (II) and mercury (II) ions of polyfluorenes with imidazole in the main chain  |  Spiliopoulos, I. K. 2019. Polymer International. 68(6): 1033-1041.
  11. A visual fluoresce covalent organic polymer for precise analysis of Fe3+ in MC3T3-E1 cells: A method for bone disease diagnosis  |  Li, W., Xu, C., Huang, L., Huang, Z., Zhou, B., Li, Y.,.. & Wang, L. 2021. Materials & Design. 212: 110243.
  12. Synthesis of linear unsubstituted poly (4, 4′‐triphenylamine) via Suzuki‐Miyaura coupling of an asymmetric AB monomer  |  Kao, T. H., Qiao, Z., Ho, P. Y., Ditzer, O., Sun, N., Voit, B., & Lissel, F. 2022. Journal of Polymer Science. 60(12): 1899-1911.
  13. Inclusion of triphenylamine unit in dopant-free hole transport material for enhanced interfacial interaction in perovskite photovoltaics  |  Lee, J. H., Jang, M. H., Lee, C. H., Lee, J. J., Lee, S. Y., & Jo, J. W. 2022. Dyes and Pigments. 200: 110162.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4,4′-Dibromotriphenylamine, 1 g

sc-396412
1 g
$55.00

4,4′-Dibromotriphenylamine, 5 g

sc-396412A
5 g
$200.00