Novel crystal modifications of yellow diazo dyestuff and process for producing thereof
Crystal modifications of a known disazo pigment are obtained by treatment at ≥ 100 degrees C of the dye or a tautomer, cis/trans isomer or tautomeric cis/trans isomer with dimethylformamide, N-methyl-pyrrolidone, dimethyl sulfoxide, 4-20C alcohols, 1,2-dichlorobenzene, pyridine and/or nitrobenzene,...
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Zusammenfassung: | Crystal modifications of a known disazo pigment are obtained by treatment at ≥ 100 degrees C of the dye or a tautomer, cis/trans isomer or tautomeric cis/trans isomer with dimethylformamide, N-methyl-pyrrolidone, dimethyl sulfoxide, 4-20C alcohols, 1,2-dichlorobenzene, pyridine and/or nitrobenzene, optionally in combination with up to 90 wt.% water. Crystal modifications of a known disazo pigment of formula (I) are obtained by treatment at ≥ 100 degrees C of (I) or a tautomer, cis/trans isomer or tautomeric cis/trans isomer with dimethylformamide, N-Me-pyrrolidone, dimethyl sulfoxide, 4-20C alcohols, 1,2-dichlorobenzene, pyridine and/or nitrobenzene optionally in combination with up to 90 wt.% water. Independent claims are also included for: (i) the yellow disazo pigment (I) whose Cu-K alpha X-ray powder diagram shows specified values for alpha , beta , gamma , delta , zeta and eta modifications; and (ii) mixtures of (I) containing ≥ 10 (especially ≥ 90) % of each of these individual modifications or of 2-6 of the modifications. |
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