Triphenylamine
From Wikipedia, the free encyclopedia
| Triphenylamine | |
|---|---|
| IUPAC name | Triphenylamine |
| Other names | N,N,N-Triphenylamine, N,N-Diphenylbenzeneamine, N,N-Diphenylaniline, TPA |
| Identifiers | |
| CAS number | [603-34-9] |
| PubChem | |
| EINECS number | |
| RTECS number | YK2680000 |
| SMILES | c1ccccc1N(c2ccccc2)c3ccccc3 |
| 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 | |
| Main hazards | Irritant (Xi) |
| R-phrases | R20/21/22 |
| S-phrases | S26, S36 |
| Flash point | 180 °C o.c. |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
|
Triphenylamine is a tertiary amine with structural formula (C6H5)3N. Its derivatives have useful properties in electrical conductivity and electroluminescence, and they are used in OLEDs as hole-transporters.[1]
[edit] References
- ^ Synthesis of Novel Triphenylamine-based Conjugated Polyelectrolytes and Their Application to Hole-Transport Layer in Polymeric Light-Emitting Diodes

