Triphendioxazine
| Structural formula | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|
|
|
||||||||||
| General | ||||||||||
| Surname | Triphendioxazine | |||||||||
| other names |
|
|||||||||
| Molecular formula | C 18 H 10 N 2 O 2 | |||||||||
| External identifiers / databases | ||||||||||
|
||||||||||
| properties | ||||||||||
| Molar mass | 286.29 g mol −1 | |||||||||
| Physical state |
firmly |
|||||||||
| safety instructions | ||||||||||
|
||||||||||
| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . | ||||||||||
Triphendioxazine is a heterocyclic compound in which five six-membered rings are fused linearly. The eponymous basic building block is 2 H -1,4-oxazine. Two such 2 H -1,4-oxazines are [1,2- b : 4,5- b ' ] fused to a benzene ring to give benzo [1,2- b : 4,5- b' ] to [1,4 ] oxazine. The annulation of two further benzene rings yields [1,4] benzoxazino [2,3- b ] phenoxazine, which is shortened, but chemically imprecise, also called dioxazine . (Not to be confused with dioxin .)
Properties and use
Triphendioxazine is the chromophore in dioxazine coloring agents , such as carbazole violet .
Individual evidence
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.