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Methyl violet 2B (Tetramethylparosanilinium chloride, 4,4'-[(4-Imino-2,5-cyclohexadien-1-yliden)methylen]bis(N,N-dimethylaniline)hydrochloride) is a violet triarylmethane dye from the group of cationic dyes and an essential component of C.I. Basic Violet 1 (trivial name methyl violet). Methyl violets are mixtures of tetramethyl (2B ...
Methyl violet is a mutagen and mitotic poison, therefore concerns exist regarding the ecological impact of the release of methyl violet into the environment. Methyl violet has been used in vast quantities for textile and paper dyeing, and 15% of such dyes produced worldwide are released to environment in wastewater. Numerous methods have been ...
Methyl violet 2B: Gentian violet B Basic violet 1 42535 triarylmethane 8004-87-3: Methyl violet 6B: 42536 triarylmethane 84215-49-6: Methyl yellow: Butter yellow Solvent yellow 2 11020 azo 60-11-7: Methylene blue: Swiss blue Basic blue 9 Solvent blue 8 52015 thiazin 61-73-4: Methylene green: Basic green 5 52020 thiazin 2679-01-8: Milling red FR ...
The name gentian violet was originally used for a mixture of methyl pararosaniline dyes (methyl violet), but is now often considered a synonym for crystal violet. The name refers to its colour, being like that of the petals of certain gentian flowers; it is not made from gentians or violets .
Victoria blue dyes are related to the methyl violet dyes, except they contain one naphthylamino group. Variation is found is dimethylamine vs diethylamino substituents on the phenyl rings and variations of the secondary amine on the naphthyl group. Victoria blue dyes
It is a magenta solid with a variety of uses as a dye. [1] It is one of the four components of basic fuchsine. (The others are rosaniline, new fuchsine and magenta II.) [2] It is structurally related to other triarylmethane dyes called methyl violets including crystal violet, which feature methyl groups on nitrogen.
p-Dimethylaminobenzophenone is related to Michler's ketone, but with only one amine. [5] Auramine O, a dye, is a salt of the iminium cation [(CH 3) 2 NC 6 H 4] 2 CNH 2 +.Michler's thione, [(CH 3) 2 NC 6 H 4] 2 CS, is prepared by treatment of Michler's ketone with hydrogen sulfide in the presence of acid or sulfideing auramine O. [6] Hydride reduction of Michler's ketone gives 4,4'-bis ...
Diverse additives are used to make it difficult to use distillation or other simple processes to reverse the denaturation. Methanol is commonly used both because its boiling point is close to that of ethanol and because it is toxic. Another typical denaturant is pyridine. Often the denatured alcohol is dyed with methyl violet. [8]