Triphenylamine

Triphenylamine
Names
IUPAC name
Triphenylamine
Other names
N,N,N-Triphenylamine, N,N-Diphenylbenzeneamine, N,N-Diphenylaniline
Identifiers
603-34-9 YesY
ChemSpider 11282 YesY
EC Number 210-035-5
Jmol interactive 3D Image
PubChem 11775
RTECS number YK2680000
Properties
C18H15N
Molar mass 245.32 g/mol
Appearance Off-white solid
Density 0.774 g/cm3
Melting point 127 °C (261 °F; 400 K)
Boiling point 347 to 348 °C (657 to 658 °F; 620 to 621 K)
Almost insoluble
log P 5.74
Hazards
Main hazards Irritant (Xi)
R-phrases R20/21/22
S-phrases S26, S36
Flash point 180 °C (356 °F; 453 K) open cup
US health exposure limits (NIOSH):
none[1]
TWA 5 mg/m3[1]
N.D.[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
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.[2]

Triphenylamine can be prepared by arylation of diphenylamine.[3]

References

  1. 1 2 3 "NIOSH Pocket Guide to Chemical Hazards #0643". National Institute for Occupational Safety and Health (NIOSH).
  2. ↑ 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
  3. ↑ F. D. Hager "Triphenylamine" Org. Synth. 1941, Coll. Vol. 1, 544.

See also

External links

This article is issued from Wikipedia - version of the Monday, November 02, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.