6375-46-8Relevant academic research and scientific papers
A 3 - (N, N - disubstituted) amino acetophenone compound of clean production method
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Paragraph 0032-0035; 0036-0038, (2017/08/31)
The invention relates to a clean production method of 3-(N,N-di-substituted)aminoacetanilide compounds (III). The method comprises the following steps: (1) adding water to a compound of Formula (I), stirring uniformly, adding alkali to regulate the pH value to 6-7 when the substituent group R1 is hydrogen or not regulating the pH value when the substituent group R1 is methoxy group, adding a compound of Formula (II) and an acid-binding agent, and reacting to the end point while controlling the pH value at 4-9 and the temperature at 60-130 DEG C; (2) separating out a compound (III) to obtain a chloride salt-containing mother solution; (3) decolorizing the chloride salt-containing mother solution by using activated carbon or by adsorbing organic matters with a resin, thereby obtaining a colorless chloride salt mother solution; and (4) recovering the chloride salt from the colorless chloride salt mother solution by MVR (mechanical vapor recompression) high-efficiency concentration cooling crystallization or multiple-effect evaporation system concentration crystallization, wherein the concentration condensation water and crystallization mother solution are respectively recycled. The method lowers the production cost, and implements resource recovery and reduction on wastewater.
A new class of light-fast oxonol dyes: Organic-glass forming salts of oxonol anions and 4,4′-bipyridinium cations
Inagaki, Yoshio,Morishima, Shin-Ichi,Wariishi, Koji,Saito, Naoki,Akiba, Masaharu
, p. 345 - 347 (2007/10/03)
A new class of light-fast oxonol dyes were prepared. These dyes were spin-coated onto glass plates using 2,2,3,3-tetrafluoro-1-propanol as a solvent to form noncrystalline-solid-dye films. They were colored, transparent, uniform, but dark when placed between crossed polarizers. The change of the normalized absorbance of dye films measured at their respective absorption maxima. The oxidative quenching mechanism is responsible for the light-fastness of the oxonol salts. The heavy-metal free and organic recording dyes with enhanced light-resistance will expand the range of potential applications for oxonol dyes.
Azo dyes containing a 3-aminobenzothienoisothiazole diazo component
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, (2008/06/13)
Dyes of the formula STR1 where R and R1 are independently of the other hydrogen, halogen, nitro, alkyl or alkoxy and KK is the radical of a coupling component, which are particularly suitable for dyeing polyester fibers if no water-solubilizing group is present, and which are particularly suitable for dyeing and printing textile materials made of polyamide fibers when at least one sulfo group is present in the dye.
Synthesis and Spectral Characterization of Blue Dyes of the Benzene Series
Thiel, W.,Mayer, R.,Jauer, E.-A.,Modrow, H.,Dost, H.
, p. 497 - 514 (2007/10/02)
53 Donor-acceptor substituted azo dyes of the benzene series were prepared by diazonium-coupling reactions (1a-s) or halogen-cyanide exchange (->2a-x, 3a-j).Described are the preparation of the amines 4a-m and the coupling compounds 5a-t and the procedure of diazotizing and coupling.The colouristic and spectroscopic data show that compounds of the general formula 1 are excellent brilliant blue azo dyes usefull for dyeing polyester material.
