Abstract:
Dye mixtures useful for dyeing or printing textile fibers or fabrics contain from 40 to 75% by weight, based on the weight of the dyes, of a dye of the formula ##STR1## where R is C.sub.1 -C.sub.4 -alkyl and n is 1 and from 25 to 60% by weight, based on the weight of the dyes, of a dye of the abovementioned formula where R is C.sub.1 -C.sub.4 -alkyl and n is 2.
Abstract:
A process for preparing diaminopyridines of the formula ##STR1## where one of the two radicals X.sup.1 and X.sup.2 is hydrogen, C.sub.1 -C.sub.4 -alkyl, halogen or nitro and the other is cyano,R.sup.1 is hydrogen, C.sub.1 -C.sub.4 -alkyl or phenyl,R.sup.2 and R.sup.3 are each hydrogen, C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -alkoxy,R.sup.4 is hydrogen or C.sub.1 -C.sub.4 -alkyl, andR.sup.5 is optionally substituted C.sub.1 -C.sub.10 -alkyl, C.sub.3 -C.sub.4 -alkenyl or C.sub.5 -C.sub.7 -cycloalkyl,by reacting dichloropyridines of the formula ##STR2## in a first step with an amine of the formula R.sup.5 -NH.sub.2 at from 10.degree. to 80.degree. C. in the presence of a base and of an inert organic diluent and/or water, then removing the diluent and thereafter, with or without prior intermediate isolation of the reaction product, comprises carrying out the second step in a melt at from 90.degree. to 165.degree. C. and at a pH from 3.5 to 6.5 using from 1.3 to 3 mol of aniline IV are used per mole of dichloropyridine II.
Abstract:
Blue dye mixtures useful for dyeing or printing polyester fabrics contain from 30 to 95% by weight, based on the total weight of the dyes, of one or more dyes based on 1,4-diaminoanthraquinone-2,3-dicarboximides and also from 5 to 70% by weight based on the total weight of the dyes, of one or more thiopheneazo dyes having a coupling component of the aniline series.
Abstract:
A process for the preparation of C.sub.4 -C.sub.10 alkyl cyanoacetates by the reaction of cyanoacetic acid with C.sub.4 -C.sub.10 alkanols at a temperature of from 35.degree. to 150.degree. C. and under a pressure of from 70 to 1013 mbar, in the presence of catalytic amounts of acid, while a C.sub.4 -C.sub.10 alkanol/water azeotrope is separated during the reaction.
Abstract:
The compounds of the general formula ##STR1## where X is fluorine, chlorine, bromine, SO.sub.2 E or unsubstituted or substituted hydroxyl or mercapto, E is alkyl, alkenyl, cycloalkyl, aralkyl, aryl, chlorine or unsubstituted or substituted hydroxyl or amino, Y is cyano, nitro, alkanoyl, aroyl, alkylsulfonyl, arylsulfonyl, carboxyl, a carboxylic ester group or unsubstituted or substituted carbamyl, T is hydrogen, C.sub.1 -C.sub.4 -alkyl, a radical which can be introduced by electrophilic substitution or a radical of the formula --CH.dbd.B, in which B is a radical of a methylene-active compound or of an amine, and K is a radical of a coupling component, are very useful for dyeing synthetic fibers or plastics.
Abstract:
Disazothiphene dyes of the formula ##STR1## where X is an electron withdrawing group, Z is an electron withdrawing group, D is the radical of a diazo component and K is the radical of a coupling component, are highly suitable for dyeing synthetic fibers, in particular polyesters.
Abstract:
Novel mono-azide substituted rylene-imide derivatives, their use in methods for the detection of analytes and reagents kits for the detection of analytes comprising said novel mono-azide substituted rylene-imide derivatives.
Abstract:
The present invention provides a compound of formula The compound of formula (1) is suitable for use as semiconducting material, in particular in electronic devices.
Abstract:
Compounds of the general formula (I) and compounds of the general formula (II) Use of compounds (I) or (II) as visible or invisible markers, for staining materials, in the laser welding of materials, for detecting bases, acids or pH changes, as a dispersing assistant, pigment additive for organic pigments and intermediates for the production of pigment additives, in heat management or energy management, in photovoltaics or in optical data storage.
Abstract:
Printing inks for offset and/or letterpress printing which comprise NIR absorbers, and solubility of the NIR absorber in the printing ink is at least 0.1% by weight. NIR absorbers consisting of cyanine cation with an anion which has long-chain alkyl or aralkyl groups. Use of such printing inks for printing processes in which the curing of the printing ink is promoted by using IR lasers. NIR absorbers comprising a cyanine cation with an anion which has long-chain alkyl or aralkyl groups.