Tetraphenyl butadiene
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IUPAC name
1,1,4,4-Tetraphenyl-1,3-butadiene
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Identifiers | |
ChemSpider | |
ECHA InfoCard | 100.014.468 |
EC Number |
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PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C28H22 | |
Molar mass | 358.475 g/mol |
Appearance | white to yellow white needles |
Density | 1.079g/cm3 |
Melting point | 203.5 °C (398.3 °F; 476.6 K) |
Boiling point | 556.1 °C (1,033.0 °F; 829.2 K) at 760 mmHg |
Solubility | soluble in ethanol, benzene, chloroform, acetic acid[1] |
Hazards | |
NFPA 704 (fire diamond) | |
Flash point | 289 °C (552 °F; 562 K) |
Safety data sheet (SDS) | Sigma-Aldrich |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tetraphenyl butadiene (IUPAC name: 1,1,4,4-tetraphenyl-1,3-butadiene, abbreviated TPB) is an organic chemical compound used as an electroluminescent dye. It glows blue with an emission spectrum peak wavelength at 430 nm,[2] which makes it useful as a wavelength shifter.[3][4]
References
- ^ Lide, David R. (1998). Handbook of Chemistry and Physics (87 ed.). Boca Raton, FL: CRC Press. pp. 3–526. ISBN 0-8493-0594-2.
- ^ W. M. Burton and B. A. Powell, "Fluorescence of Theraphenyl-Butadiene in the Vacuum Ultraviolet", Applied Optics, Vol. 12, Issue 1, pp. 87-89 (1973), doi:10.1364/AO.12.000087.
- ^ Wise, Donald Lee; Gary E. Wnek; Debra J. Trantolo; Thomas M. Cooper; Joseph D. Gresser (1998). Photonic Polymer Systems. CRC Press. p. 250. ISBN 978-0-8247-0152-9. Retrieved 2009-06-02.
- ^ Wernick, Miles N.; John N. Aarsvold (2004). Emission Tomography. Academic Press. p. 374. ISBN 978-0-12-744482-6. Retrieved 2009-06-02.