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:
The present invention relates to a process for the production of cyanine dyes with their methine chain showing group (M) and the charge compensation occuring by linked end groups through transformation of cationic cyanine dyes comprising group (D) with CH-acid compounds of the following formula (I) B.sub.1 --CH.sub.2 --B.sub.2 in an inert solvent, the substituents having the significance given in the description. ##STR1##
Abstract:
A process for the preparation of N,N'-disubstituted 1,4-diaminoanthraquinones has been found which is characterized in that 1,4-dihydroxyanthraquinones are reacted with aliphatic or aromatic amines in the presence of a hydroxycarboxylic acid as a condensation auxiliary.
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:
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.
Abstract:
Phthaloperinone dyestuffs of the general formula (I) ##STR1## wherein Z denotes SO.sub.2 or CO,A represents optionally substituted alkyl or aryl,and the other substituents have the meanings given in the description, are prepared by condensation of corresponding phthalic acids or functional derivatives thereof and optionally substituted 1,8-naphthalene-diamines.The dyestuffs according to the invention have very good fastnesses and are employed in processes for bulk dyeing plastics.
Abstract:
The process for preparing arylaminohydroxyanthraquinone of the formula by reacting appropriate chlorohydroxyanthraquinone with an amine of the formula (III) H2N—Ar (III), is characterized in that one mole of amine of the formula (III) plus an excess of 10 to 100% based on one mole of amine is used per chlorine atom in the compounds of the formula (II) and the reaction is carried out in an inert solvent in the presence of a base selected from the group consisting of the carbonates of the alkali and alkaline earth metals, the acetates of the alkali metals, the phosphates of the alkali metals and any mixtures thereof.