Abstract: The novel pigment preparations containing at least one metal azo pigment A) and at least one aliphatic monocarboxylic acid B) having 10 to 22 carbon atoms are suitable for the colouring of plastics and in this connection feature improved heat stability.

Abstract: The present invention relates to novel methine dyes, methods for the preparation thereof and use thereof for dyeing plastics, especially polyamides, so as to obtain yellow to orange colourings with improved light fastness and improved thermal stability.

Abstract: The present invention relates to novel methine dyes, methods for the preparation thereof and use thereof for dyeing plastics, especially polyamides, so as to obtain yellow to orange colourings with improved light fastness and improved thermal stability.

Abstract: The present invention relates to novel methine dyes, methods for the preparation thereof and use thereof for dyeing plastics, especially polyamides, so as to obtain yellow to orange colourings with improved light fastness and improved thermal stability. Methine dyes for example accord to the formula (I) in which R1 is hydrogen, halogen, alkyl, COOH or COOR9, R2 is oxygen or sulfur, R3 is hydrogen, halogen, COOH, COOR10 or CN, R4 is alkyl or phenyl, R5 and R6 are each independently alkyl, R7 and R8 are each independently hydrogen, halogen, alkyl or COOR11, and R9, R10 and R11 are each independently alkyl.

Abstract: The present invention relates to novel methine dyes, methods for the preparation thereof and use thereof for dyeing plastics, especially polyamides, so as to obtain yellow to orange colourings with improved light fastness and improved thermal stability.

Abstract: Novel red methine dyes, methods for the preparation thereof, and use thereof for dyeing plastics, especially vinyl polymers, provide red colourings with improved colour strengths and improved colour brilliance.

Abstract: Novel red methine dyes, methods for the preparation thereof, and use thereof for dyeing plastics, especially vinyl polymers, provide red colourings with improved colour strengths and improved colour brilliance.

Abstract: The present invention relates to novel methine dyes, methods for the preparation thereof and use thereof for dyeing plastics, especially polyamides, so as to obtain yellow colorings with improved light fastness and improved thermostability.

Abstract: The present invention relates to novel methine dyes, methods for the preparation thereof and use thereof for dyeing plastics, especially polyamides, so as to obtain yellow to orange colourings with improved light fastness and improved thermal stability.

Abstract: The present invention relates to novel methine dyes, methods for the preparation thereof and use thereof for dyeing plastics, especially polyamides, so as to obtain yellow to orange colourings with improved light fastness and improved thermal stability.

Abstract: The present invention relates to novel methine dyes, methods for the preparation thereof and use thereof for dyeing plastics, especially polyamides, so as to obtain yellow to orange colourings with improved light fastness and improved thermal stability.

Abstract: Yellow metal azo pigments based on adducts of at least two metal azo compounds provide improved dispersion properties and are of excellent suitability for pigmentation of pigment preparations for a broad field of use.

Abstract: Yellow metal azo pigments based on adducts of at least two metal azo compounds provide improved dispersion properties and are of excellent suitability for pigmentation of pigment preparations for a broad field of use.

Abstract: The new metal azo pigments comprising the adduct of a) at least two metal azo compounds of the formula (I) or their tautomeric forms in which the substituents have the definition indicated in the description, and b) at least one compound of the formula (II) in which R6 has the definition indicated in the description, are characterized in that in the X-ray diffractogram with a lattice constant of d=10.3 (±0.2) ? the metal azo pigment has a signal S1 with an intensity I1 and in the lattice constant range from d=16.05 ? to d=11.78 ? has no signal S2 whose intensity I2 in relation to the intensity I1 of signal S1, expressed as ratio I2/I1 of the background-corrected intensities, exceeds a value of 0.02, and are outstandingly suitable for producing pigment preparations and especially for producing color filters.

Abstract: The new metal azo pigments comprising the adduct of a) at least two metal azo compounds of the formula (I) or their tautomeric forms in which the substituents have the definition indicated in the description, and b) at least one compound of the formula (II) in which R6 has the definition indicated in the description, are characterized in that in the X-ray diffractogram with a lattice constant of d=10.3 (±0.2) ? the metal azo pigment has a signal S1 with an intensity I1 and in the lattice constant range from d=16.05 ? to d=11.78 ? has no signal S2 whose intensity I2 in relation to the intensity I1 of signal S1, expressed as ratio I2/I1 of the background-corrected intensities, exceeds a value of 0.02, and are outstandingly suitable for producing pigment preparations and especially for producing colour filters.

Abstract: The use of fluorine-substituted perylenes in color filters for liquid-crystal displays is described.

Abstract: Use of fluorine-substituted perylenes in colour filters for liquid-crystal displays.

Abstract: Use of quinacridones of the formula (I) in which A is an organic radical substituted by one or more fluorine atoms, B is H, F, Cl, Br or an optionally substituted organic radical which may optionally together with A form a ring in colour filters for LCDs.

Abstract: Mixtures have been found comprising at least one red dye of the formula (I), (C) or (CI) and at least one orange dye of the formula (L), (LI), (LII), (LIII), (LIV) or (LV) where the substituents have the definition in the description, these mixtures being suitable more particularly for the mass colouring of plastics.

Abstract: Process for preparing compounds of the formula (I) where R1, R2 and R3 are independently hydrogen, alkyl or cycloalkyl, characterized in that an aldehyde of the formula (II) is reacted with CH2(CN)2 in the presence of butanol.