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Vat dyes are a class of dyes that are classified as such because of the method by which they are applied. Vat dyeing is a process that refers to dyeing that takes place in a bucket or vat. The original vat dye is indigo , once obtained only from plants but now often produced synthetically.
Furthermore, the quality of the new dyes increased. Chemist Rene Bohn developed a brilliant blue vat dye, indanthrone, with excellent color fastness in 1901. BASF(Badische Anilin und Soda Fabrik), the largest manufacturer of vat dyes, sold it as Indanthren Blue RS, along with the synthetic indigo they placed on the market in 1897. [19]
Indanthrone is utilized as a blue pigment (C.I. Pigment Blue 60), primarily in the process of vat dyeing, often referred to as C.I. Vat Blue 4. [8] Indanthrone is a vat dye, synthesized to provide highest color fastness for the dyeing and printing of predominantly cellulose-based textile fibers. Fabrics dyed with indanthrene fulfill the highest ...
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A dye is a colored substance that chemically bonds to the substrate to which it is being applied. This distinguishes dyes from pigments which do not chemically bind to the material they color. Dye is generally applied in an aqueous solution and may require a mordant to improve the fastness of the dye on the fiber. [2]
Anthraquinone dyestuffs are structurally related to indigo dyestuffs and are classified together with these in the group of carbonyl dyes. [2] Members of this dye group can be found in natural dyes as well as in synthetic dyes. Anthraquinone dyestuffs are represented in mordant and vat, but also in reactive and disperse dyes.
Vat brown 1 70802 anthraquinone 2475-33-4: Vat Green 1: Jade green base Vat green 1 59825 anthraquinone 128-58-5: Vat Green 9: Vat black BB Vat green 9 59850 anthraquinone 6369-65-9: Vat Orange 1: Vat golden yellow RK Vat orange 1 59105 anthraquinone 1324-11-4: Vat Yellow 1: Flavanthrone Indofast yellow Vat yellow 1 70600 anthraquinone 475-71-8 ...
Vat Blue 36 is a vat dye that is chemically related to indigo. It is produced by condensation of 4-methyl-5-chloro-7-methoxy-3-indolinone and 5,7–dichloro-3-(2H)-thianaphthenone . [ 1 ]