2-aminodiphenylamine
Structural formula | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
![]() |
||||||||||||||||
General | ||||||||||||||||
Surname | 2-aminodiphenylamine | |||||||||||||||
other names |
|
|||||||||||||||
Molecular formula | C 12 H 12 N 2 | |||||||||||||||
Brief description |
red-brown solid |
|||||||||||||||
External identifiers / databases | ||||||||||||||||
|
||||||||||||||||
properties | ||||||||||||||||
Molar mass | 184.24 g mol −1 | |||||||||||||||
Physical state |
firmly |
|||||||||||||||
Melting point |
75-78 ° C |
|||||||||||||||
boiling point |
106-108 ° C (0.5 hPa) |
|||||||||||||||
solubility |
|
|||||||||||||||
safety instructions | ||||||||||||||||
|
||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
2-aminodiphenylamine is a chemical compound from the aminobenzenes group .
Extraction and presentation
2-aminodiphenylamine can be obtained by reacting 1-chloro-2-nitrobenzene with aniline and then reducing it.
properties
2-aminodiphenylamine is a red-brown solid that is practically insoluble in water. It decomposes when heated.
use
2-aminodiphenylamine is used as an intermediate in organic synthesis and pharmacy .
Individual evidence
- ↑ a b c d e f Entry on 2-aminodiphenylamine in the GESTIS substance database of the IFA , accessed on October 19, 2019(JavaScript required) .
- ↑ a b c d e data sheet N-Phenyl-o-phenylenediamine, 98% from AlfaAesar, accessed on October 19, 2019 ( PDF )(JavaScript required) .
- ^ GA Swan: Phenazines . John Wiley & Sons, 2009, ISBN 0-470-18810-3 , pp. 5 ( limited preview in Google Book search).