Abstract: Mixtures of fiber-reactive dyes, preparation thereof and use thereof for dyeing fiber materials The present invention relates to dye mixtures comprising one or more dyes of the general formula (I) and one or more dyes of the general formula (II) where B, M, R1, R2, R3, R4, X, Y, Z1, Z2, Z3 and Z4 are each as defined in claim 1, processes for their preparation, and their use for dyeing or printing hydroxyl- and/or carboxamido-containing material.

Abstract: Described are fiber-reactive, water-soluble monoazo compounds which conform to the hereinbelow indicated and defined general formula (1) and which are capable of dyeing hydroxy- and/or carboxamido-containing material, especially fiber material, such as cellulose fibers, for example cotton or regenerated cellulose fibers, and also wool and synthetic polyamide fibers in high color strength and good fastnesses. ##STR1## where M is hydrogen, an alkali metal or some other salt-forming, colorless metal, D is a 2-sulfophenyl radical which may be additionally substituted by alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, sulfo and/or carboxy or is a 1-sulfonaphth-2-yl radical which may be additionally substituted by sulfo and/or carboxy, and the group --SO.sub.2 --Y is a fiber-reactive group of the vinyl sulfone series.

Abstract: The disclosed dyes (which are fiber-reactive and are useful for dyeing materials containing OH and/or carboxamide groups) are compounds of the formula (1)Fb--Z.sub.n (1)in which:Fb is the radical of various classes of dyestuffs, including the formazans, azomethines, phthalocyanines, etc., and particularly sulfo group-containing monoazo or disazo dyes of the formulas (a-1) through (a-5):D.sup.1 --N.dbd.N--K.sup.2 -- (a-1)--D.sup.2 --N.dbd.N--(E--N.dbd.N).sub.v --K.sup.1 (a-2)--D.sup.2 --N.dbd.N--(E--N.dbd.N).sub.v --K.sup.2 -- (a-3)D.sup.1 --N.dbd.N--K.sup.0 --N.dbd.N--D.sup.2 -- (a-4)--D.sup.1 --N.dbd.N--K.sup.0 --N.dbd.N--D.sup.2 -- (a-5)in which in which D.sup.1 is a substituted or unsubstituted phenyl or naphthyl radical, D.sup.2 is the radical of a diazo component and K.sup.1, K.sup.2, and K.sup.0 are various coupling components, and E is a middle component.

Abstract: Dyes containing a 5,6-difluoropyrimidin-4-yl radical as fiber-reactive group are useful for dyeing hydroxy- and/or carboxamido-containing material, including fiber material, for example cellulose fibers, wool and polyamide.

Abstract: Improved unsymmetric reactive dyestuffs have the following formula ##STR1## wherein Y.sub.1 is a radical of the formula ##STR2## and wherein the other substituents have the meaning given in the description.

Abstract: Dyes of the formula (1) indicated and defined below, containing at least one sulfo group, which can be used for dyeing hydroxy and/or carboxamido-containing material, especially fiber material, for example cellulosic fiber materials, wool and synthetic polyamide. ##STR1## in which F is the radical of a dye molecule, n is the number 1 or 2, R.sup.A is hydrogen or substituted or unsubstituted lower alkyl, R.sup.B is hydrogen, unsubstituted or substituted lower alkyl or unsubstituted or substituted phenyl, X is halogen, R is hydrogen, lower alkyl, lower alkoxy halogen or sulfo, and G at the benzene ring forms the radical of a heterocycle which includes at least one carbonylamido group whose N atom can be substituted.

Abstract: Process for preparing 2,4,6-trichloropyrimidine, characterized in that, in a first reaction step, barbituric acid is reacted, optionally in the presence of a catalyst, with phosphorus oxychloride and subsequently, in a second reaction step, with phosphorus pentachloride or with reactants forming the latter, in particular phosphorus trichloride and chlorine.

Abstract: Fibre-reactive dyestuffs based on barbituric acid, of the following formula ##STR1## wherein the substituents have the meaning given in the description, are distinguished by improved properties.

Abstract: Reactive dyestuff mixtures containing one or more monochlorotriazine dyestuffs of the formula (1) ##STR1## and one or more monofluorotriazine dyestuffs of the formula (2) ##STR2## in which the substituents have the meaning given in the description, show on-tone exhaustion onto fibres and are fixed uniformly even under different fixation conditions.