- Triphenylamine
-
Triphenylamine TriphenylamineOther namesN,N,N-Triphenylamine, N,N-Diphenylbenzeneamine, N,N-Diphenylaniline, TPAIdentifiers CAS number 603-34-9 PubChem 11775 ChemSpider 11282 EC number 210-035-5 RTECS number YK2680000 Jmol-3D images Image 1 - c3c(N(c1ccccc1)c2ccccc2)cccc3
Properties Molecular formula C18H15N Molar mass 245.32 g/mol Appearance Off-white solid Density 0.774 g/cm3 Melting point 127 °C
Boiling point 347 - 348 °C
Solubility in water Almost insoluble log P 5.74 Hazards R-phrases R20/21/22 S-phrases S26, S36 Main hazards Irritant (Xi) Flash point 180 °C o.c. (verify) (what is: / ?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)Infobox references Triphenylamine is an organic compound with formula (C6H5)3N. In contrast to most amines, triphenylamine is nonbasic. Its derivatives have useful properties in electrical conductivity and electroluminescence, and they are used in OLEDs as hole-transporters.[1]
Triphenylamine can be prepared by arylation of diphenylamine.[2]
References
- ^ Wei Shi, Suqin Fan, Fei Huang, Wei Yang, Ransheng Liu and Yong Cao "Synthesis of Novel Triphenylamine-based Conjugated Polyelectrolytes and Their Application to Hole-Transport Layer in Polymeric Light-Emitting Diodes" J. Mater. Chem., 2006, 16, 2387-2394. doi:10.1039/B603704F
- ^ F. D. Hager "Triphenylamine" Org. Synth. 1941, Coll. Vol. 1, 544.
See also
External links
This article about an amine is a stub. You can help Wikipedia by expanding it.