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In a reactive dye, a chromophore (an atom or group whose presence is responsible for the colour of a compound) contains a substituent that reacts with the substrate. Reactive dyes have good fastness properties owing to the covalent bonding that occurs during dyeing. Reactive dyeing is the most important method for coloring cellulose fibers.
Reactive blue 4 61205 anthraquinone 13324-20-4: BODIPY: Dipyrrometheneboron difluoride 138026-71-8: Brazilin/Brazilein: Natural red 24 75280 natural 474-07-7: Brilliant Black BN: Food Black 1 28440 diazo 2519-30-4: Brilliant blue FCF: Erioglaucine FD&C Blue No. 1 Acid blue 9 Food blue 2 42090 triarylethlamine 3844-45-9: Brilliant cresyl blue ...
If the vinyl sulfone group is introduced via a primary or secondary aliphatic amine, this is performed again by condensation with a halotriazine compound. An example is 2-[2-(2-chlorethylsulfonyl)ethoxy]ethanamine used in bifunctional reactive dyes in combination with a monofluoro or monochlorotriazine hook. [3]
Examples of acid dye are Alizarine Pure Blue B, Acid red 88, etc. Basic dyes are water-soluble cationic dyes that are mainly applied to acrylic fibers, but find some use for wool and silk. Usually acetic acid is added to the dye bath to help the uptake of the dye onto the fiber. Basic dyes are also used in the coloration of paper.
reactive dye Reactive dyes are a class of synthetic dyes that first appeared commercially in 1956, after their invention in 1954 by Rattee and Stephens at the Imperial Chemical Industries Dyestuffs Division site in the United Kingdom. Reactive dyes are used primarily to dye natural fibers and cellulose fibers such as rayon. [39] resist dyeing
Reactive dye printing is a method of printing fabrics using reactive dye incorporated into a paste or wax including components such as sodium alginate gum, soda ash, urea and kerosin. Typically, the dye is dried at 130 degrees and cured at 180 degrees to permanently bond it, and the fabric later treated with a softener for better hand feel.
"Evidence shows cancer in laboratory male rats exposed to high levels of FD&C Red No. 3." What is red dye No. 3? Red No. 3 , approved for use in foods in 1907, is made from petroleum.
One of the most important anthraquinone dyes of herbal origin is alizarin, which is extracted from the dyer's madder (Rubia tinctorum). Alizarin is the eponym for a number of structurally related dyes that use alizarin dyes (sometimes synonymous with anthraquinone dyes). It was the first natural dye for which an industrial synthesis was ...