WHEREIN R1 IS HYDROGEN, LOWER ALKYL, ARYL, ARALKYL OR CYCLOALKYL, WHICH MAY BE SUBSTITUTED BY LOWER ALKYL OR HALOGEN, R2 IS LOWER ALKYL, R3 IS HYDROGEN OR LOWER ALKYL AND A IS A BENZENE NUCLEUS SUBSTITUTED BY LOWER ALKYL, LOWER ALKOXY ON HALOGEN. SAID PIGMENTS CAN BE USED, FOR EXAMPLE, FOR DYEING OR PRINTING PLASTICS, CAOUTCHOUC, NATURAL AND SYNTHETIC RESINS TEXTILE FIBROUS MATERIALS OR PAPER. FUTHERMORE THEY CAN 12BE EMPLOYED FOR THE PREPARATION OF PRINTING INKS, LACQUERS AND DISPERSION PAINTS. THE NOVEL PIGMENTS POSSESS GOOD TO VERY GOOD FASTNESS PROPERTIES.
WHEREIN X1 AND X2 MAY BE IDENTICAL OR DIFFERENT AND REPRESENT A HYDROGEN ATOM, A LOWER ALKYL OR ALKOXY GROUP HAVING PREFERABLY 1 TO 4 CARBON ATOMS, OR A HALOGEN ATOM PERFERABLY A CHLORINE OR BROMINE ATOM, AND R IS A HYDROGEN OR HALOGEN ATOM, METHOXY OR ETHOXY GROUP, N REPATOM, A METHYL, ETHYL, METHOXY OR ETHOXY GROUP, N REPRESENTS THE NUMBERS 1 OR 2 AND A AN OPTIONALLY SUBSTITUTED RADICAL, PREFERABLY OF THE BENZENE, NAPHTHALENE OR BENZIMIDAZOLONE SERIES OF N=1, AND OF THE BENZENE OR DIPHENYL SERIES IF N=2. THESE DYESTUFFS MAY BE USED FOR DYEING OR PRINTING LACQUERS, POLYMERS OR TEXTILE MATERIALS, THEY SHOW A GOOD FASTNESS TO LIGHT, TO WEATHER AND TO MIGRATION. FURTHERMORE, THEY ARE FAST TO HEAT, HAVE A HIGH TINCORIAL STRENGTH TO THE INFLUENCE OF CHEMICAL PRODUCTS, ESPECIALLY SOLVENTS, ACIDS AND ALKALIS.
IN WHICH X1 AND X2 ARE EQUAL OR DIFFERENT AND REPRESENT A HYDROGEN ATOM, A LOWER ALKYL OR ALKOXY GROUP HAVING 1-4 CARBON ATOMS OR A HALOGEN ATOM, PREFERABLY A CHLORINE OR BROMINE ATOM, AND R REPRESENTS A HYDROGEN OR HALOGEN ATOM, PREFERABLY, A CHLORINE OR BROMINE ATOM, A METHYL, ETHYL, METHOXY OR ETHOXY GROUP. THEY MAY BE PREPARED BY REACTING BENZENESULFOCHLORIDES OF THE GENERAL FORMULA
(A,X1,X2-PHENYL)-SO2-CL
WITH 5-AMINO-BENZIMIDAZOLONES OF THE GENERAL FORMULA
2-(O=),5-NH2,R-BENZIMIDAZOLINE
IN WHICH FORMULAE A REPRESENTS A NITRO OR ACETYLAMINO GROUP AND X1, X2 AND R ARE DEFINED AS ABOVE, AND HYDROLYSING THE ACETYL GROUP IN THE PRODUCTS THUS OBTAINED OR REDUCING THE NITRO GROUP TO THE AMINO GROUP. THESE 5 - (AMINOBENZENESULFONYLAMINO) - BENZIMIDAZOLONES CAN BE COUPLED IN THEIR DIAZOTIZED FORM WITH N-ACETOACETYLAMINO COMPOUNDS OF THE BENZENE-, DIPHENYLAND BENZIMIDAZOLONE SERIES TO MONO AND DISAZO PIGMENTS WHICH ARE DISTINGUISHED BY EXCELLENT PROPERTIES OF FASTNESS AND VERY PURE AND BRILLIANT SHADES.
Abstract:
MIXTURES OF DISAZO DYESTUFFS OBTAINED BY COUPLING DIAZOTIZED 3,3''-DICHLORO-4,4''DIAMINO-DIPHENYL WITH A MIXTURE CONSISTING OF ONE OR TWO POLAR COUPLING COMPONENTS OF THE ACETOACETYLAMINO-BENZENE AND 1 - ARYL-PYRAZONEL - (5) SERIES CONTAINING CARBOXY AND/OR SULFONIC ACID GROUPS AND ANOTHER MIXTURE CONSISTING OF ONE OR TWO NON POLAR COUPLING COMPENENTS OF THE ACETOACETYLAMINO-BENZENE AND 1-ARYL-PYRAZOLONE-(5) SERIES WITHOUT ANY WATER-SOLUBILIZING GROUPS. THESE DYESTUFF MIXTURES SHOW IMPROVED RHEOLOGICAL PROPERTIES AND AN IMPROVED TINCTORIAL STRENGTH. MOREOVER, THEY YIELD PURER SHADES AND HAVE AN INCREASED TRANSPARANCY.
Abstract:
A process for improving the properties of Pigment Yellow 17 (Colour Index 21 105) wherein an aqueous suspension of the crude dyestuff prepared in the usual manner by coupling tetrazotized 4,4''-diamino-3,3''-dichloro-diphenyl with 1-acetoacetylamino-2methoxy-benzene is heated for several hours to temperatures between 100* and 200*, preferably 100*C to 150*C, at a pH-value higher than 8, preferably at about 11. Pigment Yellow 17 aftertreated in this way has an essentially better fastness to light than the untreated pigment. Furthermore, the graphic prints produced with it have a higher lustre.
WHEREIN D IS A RADICAL OF THE TEREPHTHALIC ACID MONO AMIDE SERIES AND X1, X2 AND X3 ARE HYDROGEN, HALOGEN, ALKYL OR ALKOXY. SAID PIGMENTS CAN BE USED, FOR INSTANCE, FOR THE DYEING, PRINTING OR COLORING OF LAKES, LAKE-FORMERS, SOLUTIONS OR PRODUCTS MADE OF ACETYL CELLULOSE, NATURAL OR SYNTHETIC RESINS, POLYSTYRENE, POLYOFEFINS, POLYACRYLIC COMPOUNDS, POLYVINYL COMPOUNDS, POLYESTERS, RUBBER, CASEIN OR SILICONE RESINS, TEXTILE FIBERS, CELLULOSE ETHERS OR ESTERS, POLYAMIDES, POLYURETHANES OR PAPER. THESE DYESTUFFS SHOW GOOD FASTNESS PROPERTIES TO LIGHT, WEATHER AND MIGRATION; AND ARE RESISTANT TO THE INFLUENCE OF SOLVENTS ACIDS AND ALKALIS.
Abstract:
Monoazo pigments of the general formula WHEREIN X is hydrogen or halogen, preferably chlorine or bromine, alkyl, alkoxy, trifluoromethyl, phenyl, phenoxy or cyano, Y represents hydrogen or halogen, preferably chlorine or bromine, alkyl, alkoxy, carbomethoxy, phenyl or phenoxy, Z represents hydrogen, chlorine or bromine, alkyl, alkoxy, nitro, cyano, trifluoromethyl, methylsulfonyl, aminocarbonyl, alkylaminocarbonyl, phenylaminocarbonyl, aminosulfonyl, alkylaminosulfonyl, alkanoylamino or aroylamino, A represents a phenyl or naphthalene ring, n represents 1 or 2, m is an integer of from 1 to 3 and Me is an equivalent of a metal cation forming a lake and a process for preparing them by diazotizing aromatic amines of the general formula with coupling components of the general formula AND SUBSEQUENTLY CONVERTING INTO A LAKE WITH METAL SALTS, X,Y,Z,A, n and m having the above meaning. These pigments can be successfully used for dyeing all materials usually dyed with pigments. They are especially suitable for coloring high molecular plastics such as PVC and on account of their excellent resistance to heat, for coloring polyolefins.
Abstract:
Process for the aftertreatment of the azo pigment of the formula C.I. PIGMENT ORANGE 36 wherein the crude pigment obtained after coupling is heated to temperatures from 100 DEG to 150 DEG C. in dry or wet condition in a solvent which is water-immiscible or not indefinitely water-miscible and the pigment is isolated in known manner. The pigment aftertreated in this way shows substantially improved hiding power while the same pigment prepared in the usual way has poor hiding power and can not be used in stoving lacquers.
Abstract:
1339068 Disazo pigment mixtures FARBWERKE HOECHST AG 19 April 1971 [14 March 1970] 24056/71 Heading C4P The invention comprises the mixtures of disazo dyes obtained by coupling tetrazotized 4,4 1 -diamino-3,3 1 -dichlorodiphenyl with a mixture of coupling components consisting of (a) 0À5 to 20 mol. per cent of components H-X or H-Y or mixtures thereof and (b) 99À5 to 80 mol. per cent of components H-A or H-B or mixtures thereof, wherein A, B, X and Y are acetoacetylaminoaryl or 1-aryl-5-pyrazolone radicals, X and Y containing 1 or 2 COOH or SO 3 H groups and A and B or X and Y are always different. The products are yellow pigments and are used to colour printing inks or varnishes and in the mass dyeing of synthetic polymers.