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PRIMULINE , a dye-stuff containing the thiazole See also:ring See also:system conjointly with a See also:benzene ring. The primulines are to be considered as derivatives of dehydrothiotoluidine (aminobenzenyltoluylmercaptan), which is obtained when See also:para-tolui- S\ CH „/\/ •CBH4.NH,(p) \/\N/ Primuline. dine is heated with See also:sulphur for eighteen See also:hours at 18o–xgo C. and then for a further six hours at 200–2200 C. (P. Jacobson, Ber., 1889, 22, p. 333; L. Gattermann, ibid. p. 1084). Dehydrothiotoluidine is not itself a dye-stuff, but if the See also:heating be carried out at a higher temperature in the presence of more sulphur, then a See also:base is formed, which gives primuline yellow on sulphonation (A. G. See also:Green, Journ. See also:Soc. Chem. Ind., 1888, r, p. 194). Primuline-yellow is a mixture of See also:sodium salts and probably contains in the See also:molecule at least three thiazole rings in See also:combination. It is a substantive See also:cotton dye of rather fugitive shade, but can be diazotized on the fibre and then See also:developed with other components, so yielding a See also:series of ingrain See also:colours. Thioflavine T is obtained by the methylation of dehydrothiotoluidine with methyl See also:alcohol in the presence of hydrochloric See also:acid [See also:German Patent 51738 (1888)]. Thioflavine S results from the methylation of dehydrothiotoluidine sulphonic acid. This sulphonic acid on oxidation with See also:bleaching See also:powder or with See also:lead peroxide, in alkaline See also:solution yields chloramine yellow, which dyes cotton a beautiful yellow. Additional information and CommentsThere are no comments yet for this article.
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