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1,1,4,4-Tetraphenyl-1,3-butadiene

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For Research Use Only | Not For Clinical Use
CATAP1450631
CAS1450-63-1
Structure
MDL NumberMFCD00004766
Molecular Weight358.47
EC Number215-914-7
InChI KeyKLCLIOISYBHYDZ-UHFFFAOYSA-N
REAXYS Number1914229
Descriptionsuitable for scintillation, ≥99%
Assay≥99%
Linear Formula(C6H5)2C=CHCH=C(C6H5)2
MP207-209 °C (lit.)
Size5G
1

Anisotropic Optical Functions of α-1,4,4-tetraphenyl-1,3-butadiene

Silvia Tavazzi, Stefano Mora, Laura Alessandrini, Leonardo Silvestri

J Chem Phys. 2011 Jan 21;134(3):034707.

PMID: 21261384

1

Bridged silver(I) Complexes of the Polycyclic Aromatic Compounds Tetraphenylethylene and 1,1,4,4-tetraphenyl-1,3-butadiene

I Ino, L P Wu, M Munakata, T Kuroda-Sowa, M Maekawa, Y Suenaga, R Sakai

Inorg Chem. 2000 Nov 27;39(24):5430-6.

PMID: 11154557

1

Polarized Absorption, Spontaneous and Stimulated Blue Light Emission of J-type Tetraphenylbutadiene Monocrystals

Silvia Tavazzi, Leonardo Silvestri, Luciano Miozzo, Antonio Papagni, Peter Spearman, Sandra Ianelli, Alberto Girlando, Andrea Camposeo, Marco Polo, Dario Pisignano

Chemphyschem. 2010 Feb 1;11(2):429-34.

PMID: 20029880

1

Solvent Effects on the Absorption and Fluorescence Spectra of Some Laser Dyes: Estimation of Ground and Excited-State Dipole Moments

J Thipperudrappa, D S Biradar, S R Manohara, S M Hanagodimath, S R Inamadar, R J Manekutla

Spectrochim Acta A Mol Biomol Spectrosc. 2008 Mar;69(3):991-7.

PMID: 17714982

1

Toward Quantitative Prediction of Molecular Fluorescence Quantum Efficiency: Role of Duschinsky Rotation

Qian Peng, Yuanping Yi, Zhigang Shuai, Jiushu Shao

J Am Chem Soc. 2007 Aug 1;129(30):9333-9.

PMID: 17622142

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