Vat Violet 10

commonly known as Isoviolanthrone.(a) 7H-benzo[de]anthracen-7-onechlorinated, with Potassium hydroxide of Etanol solution treatment; (b) 7H-benzo[de]anthracen-7-oneand Potassium hydroxide of Etanol solution in Xylene, Chlorobenzene or kerosene in heating; (c) 3-Chloro-7H-benzo[de]anthracen-7-onethe anthrone into corresponding sulfide or selenide and then use alkali treatment.

Isoviolanthrone , Formerly prepared from 3- halobenzanthrone by alcoholic potash melt. Isomer-free isoviolanthrone is obtained by an alcoholic potash melt of 3,3'-dibenzanthronyl sulfide or by the one-pot method .
Dichlorination of isoviolanthrone with sulfuryl chloride, or alternatively bromination in chlorosulfonic acid, affords brilliant violet vat dyes and pigments.

Dissolve isoviolanthrone in 98% H2SO4 and precipitate it by adding water to reduce the acid concentration to about 90%. It sublimes in vacuo to give dark green-violet needles [Parkyns & Ubblehode J Chem Soc 4188 1960]. [Beilstein 7 I 465, 7 II 815, 7 III 4538, 7 IV 2747.]

blue light purple. Soluble in 2 – Chlorophenol, Xylene to red, fluorescence, slightly soluble in Acetone, Chloroform, Pyridine and Toluene, insoluble in Etanol. In concentrated sulfuric acid for SAP green, purple precipitation after dilution, In the basic insurance powder solution for dark red light blue, in acid insurance powder solution for wine.

Standard	Ironing Fastness	Chlorine bleach	Light Fastness	Mercerized	Oxygen bleach	Soaping
						Fading	Stain
ISO	3	5	5-6	4	4-5