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1,1,4,4-Tetraphenyl-1,3-butadiene (CAS 1450-63-1)

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Alternate Names:
TPB
Application:
1,1,4,4-Tetraphenyl-1,3-butadiene is a compound used for scintillation
CAS Number:
1450-63-1
Purity:
99%
Molecular Weight:
358.47
Molecular Formula:
C28H22
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1,1,4,4-Tetraphenyl-1,3-butadiene is a compound used for scintillation. 1,1,4,4-Tetraphenyl-1,3-butadiene is a conjugated diene characterized by alternating single and double bonds, which, along with its phenyl rings, imparts stability to its structure. In biological research, it serves as a fluorescent dye, enabling visualization of specific molecules or cellular components. In polymer research, it acts as a photostabilizer, enhancing the resistance of polymers to degradation caused by light exposure. Moreover, in organic synthesis, it serves as a photoreactive material, facilitating the generation of desired compounds. Furthermore, it plays a role in the synthesis of other compounds, including terphenyls, phenylthiophenes, and phenylacetylenes.


1,1,4,4-Tetraphenyl-1,3-butadiene (CAS 1450-63-1) References

  1. 1, 4‐Diphenyl‐1, 3‐butadiene and 1, 1, 4, 4‐Tetraphenyl‐1, 3‐butadiene in the Reactions of Oxidative Sulfamidation and Trifluoroacetamidation  |  Dr. Mikhail Yu. Moskalik, Dr. Vera V. Astakhova, Dr. Irina V. Sterkhova, Prof. Bagrat A. Shainyan.. 4662-4666.
  2. Bridged silver(I) complexes of the polycyclic aromatic compounds tetraphenylethylene and 1,1,4,4-tetraphenyl-1,3-butadiene.  |  Ino, I., et al. 2000. Inorg Chem. 39: 5430-6. PMID: 11154557
  3. Electrochemistry of 1,1,4,4-tetraphenyl-1,3-butadiene, 1,1,4,4-tetraphenyl-1,2-butadiene, and 1,1,4,4-tetraphenyl-1-butene in dimethylformamide  |  Tsu-yu Raymond Chen, Mark R. Anderson, Dennis G. Peters. 1986. Journal of Electroanalytical Chemistry and Interfacial Electrochemistry. 197: 341-358.
  4. Electrochemically induced isomerization of 1,1,4,4-tetra-phenyl-1,2-butadiene to 1,1,4,4-tetraphenyl-1,3-butadiene: An indirect self-protonation mechanism  |  Matthew L. Vincent, Dennis G. Peters. 1992. Journal of Electroanalytical Chemistry. 328: 63-73.
  5. Reactivity of radical-anions and dianions derived from electrochemical reduction of tetraphenylbutatriene and 1,1,4,4-tetraphenyl-1,3-butadiene  |  Matthew L. Vincent, Dennis G. Peters. 1992. Journal of Electroanalytical Chemistry. 324: 93-106.
  6. Blue light emitting diode with 1,1,4,4-tetraphenyl-1,3-butadiene (TPB)  |  Jung-Hyun Kim a, Sokwon Noh a, Kwanju Kim b, Sung-Taek Lim a, Dong-Myung Shin a. 2001. Synthetic Metals. 117: 227-228.
  7. Spectroscopic and Structural Characterization of Two Polymorphs of 1,1,4,4-Tetraphenyl-1,3-butadiene  |  Alberto Girlando*†, Sandra Ianelli†, Ivano Bilotti‡, Aldo Brillante‡, Raffaele G. Della Valle‡, Elisabetta Venuti‡, Marcello Campione§, Stefano Mora§, Leonardo Silvestri§, Peter Spearman§, and Silvia Tavazzi§. 2010. Cryst. Growth Des. 10: 2752–2758.
  8. Melt-growth of 1,1,4,4-tetraphenyl-1,3-butadiene crystals on different substrates  |  Stefano Mora a, Silvia Tavazzi a, Peter Spearman a b. 2012. Synthetic Metals. 162: 1737-1740.
  9. Exploration of the polymorph landscape for 1,1,4,4-tetraphenyl-1,3-butadiene  |  A. Bacchi,*a A. Brillante,b D. Crocco,a M. R. Chierotti,c R. G. Della Valle,b A. Girlando,a M. Masino,a P. Pelagattia and E. Venutib . 2014. CrystEngComm. 16: 8205-8213.
  10. Growth and characterization of 1, 1, 4, 4-tetraphenyl-1, 3-butadiene organic scintillation crystal  |  D. Arun kumar, S. Kalainathan & Ravi Shanker Babu. 2019. Journal of Materials Science: Materials in Electronics. 30: 10571–10578.
  11. Growth and characterization of organic scintillation single crystal 1, 1, 4, 4-Tetraphenyl-1, 3-Butadiene (TPB) using vertical Bridgman technique  |  D. Arun Kumar, Ravi Shanker Babu, S. Kalainathan. 2020. Optical Materials. 109.
  12. Effects of alpha particle and gamma irradiation on the 1,1,4,4-tetraphenyl-1,3-butadiene wavelength shifter  |  Yikui Fan a b, Chao Wen b, Jian Wu a, Zheng Li a, Yonggang Liu c, Hui Gao a, Meng Li a, Lina Zeng a, Haojun Zhou a, Shaofeng Dai a, Qilin Xie a, Xiaoqiang Fan a. 2020. Radiation Physics and Chemistry. 176.
  13. Ultraviolet-induced fluorescence of poly(methyl methacrylate) compared to 1,1,4,4-tetraphenyl-1,3-butadiene down to 4 K  |  E. Ellingwood a b, H. Benmansour a, Q. Hars a, J. Hucker a, V. Pereymak a, J.M. Corning a, P. Perrin a, G.R. Araujo c, P.C.F. Di Stefano a, M. Kuźniak d e b, T.R. Pollmann f c, M. Hamel g, M.G. Boulay e, B. Cai e 1, D. Gallacher e 2, A. Kemp a b, J. Mason e, P. Skensved a b, M. Stringer a b. 2022. Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment. 1039.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1,1,4,4-Tetraphenyl-1,3-butadiene, 5 g

sc-213420
5 g
$203.00