The symmetrical diaminophenazine is the parent substance of the important dyestuff toluylene red or dimethyldiaminotoluphenazine.
The colour produced is generally of a greenish shade; for example, nitrosobenzene is green when fused or in solution (when crystalline, it is colourless), and dinitrosoresorcin has been employed as a dyestuff under the names " solid green " and " chlorine."
Phenyl-acridine is the parent base of chrysaniline, which is the chief constituent of the dyestuff phosphine (a bye-product in the manufacture of rosaniline).
FUCHSINE, or Magenta, a red dyestuff consisting of a mixture of the hydrochlorides or acetates of pararosaniline and rosaniline.
Hofmann having previously shown that oxidation of pure aniline alone or of pure toluidine yielded no fuchsine, whilst oxidation of a mixture of aniline and para-toluidine gave rise to the fine red dyestuff para-fuchsine (pararosaniline hydrochloride) CH 3 C 6 H 4 NH 2 +2C 6 H 5 NH 2 +30 = HOC(C 6 H 4 NH 2) 3 +2H20.
Phenanthrenequinone).Alizarin black,C l oH 4 (OH) 2 0 2 NaHS03, the sodium bisulphite compound of 7.8 dioxy-anaphthoquinone, is a dyestuff used for printing on cotton in the presence of a chromium mordant The naphthoquinone is prepared by the action of zinc and concentrated sulphuric acid on a-dinitronaphthalene.
Its value as a dyestuff depends on its power of forming insoluble compounds (lakes) with metallic oxides.
C6h2(Oh)2[I.2], C]] a vegetable dyestuff formerly prepared from madder root (Rubia tinctorum) which contains a glucoside ruberythric acid (C26H28014).
The melt is dissolved in water and the dyestuff is liberated from the sodium salt by hydrochloric or sulphuric acid, or is converted into the calcium salt by digestion with hot milk of lime, then filtered and the calcium salt decomposed by acid.
PICRIC ACID, or [[Trinitrophenol, C6h2 Oh]] (N02)3 [220.127.116.11], an explosive and dyestuff formed by the action of concentrated nitric acid on indigo, aniline, resins, silk, wool, leather, &c. It is the final product of the direct nitration of phenol, and is usually prepared by the nitration of the mixture of phenol sulphonic acids obtained by heating phenol with concentrated sulphuric acid (E.