Abstract:
A process for the preparation of an azo dye of formula ##STR1## wherein K is the .beta.-naphthol radical, X is hydrogen or nitro and M is an alkali metal ion or an ammonium ion, which process comprises coupling an aqueous solution containing 15 to 30 percent by weight of a diazo component of formula ##STR2## and 6 to 20 mol % of an ammonium salt, based on the molar amount of the diazo component, at a pH in the range from 10.5 to 11.5 and in an inert gas atmosphere, to a coupling component of formula ##STR3## in which formulae (2) and (3) above K and X are as defined for formula (1).The present invention makes it possible to obtain the claimed azo dyes in high yield.
Abstract:
A process for preparing the compound, or dye, ##STR1## by forming aminoazobenzene employing a slight excess of sodium nitrite in the diazotization of aniline and, without isolation, diazotizing the monoazo base and coupling the diazonium salt into phenol.
Abstract:
An arylaminosulfonic acid is diazotized in a mineral acid with sodium nitrite, the pH at completion of diazotization being below about 0.5. An aryl, primary amino-group-containing coupler is added to the diazotization mass and coupling to the benzene ring completed in at least three stages by gradually raising the temperature to 20*-30*C., maintaining a pH below 1.5.
Abstract:
A process in which a diarylide pigment composition is produced by coupling a tetrazotised pigment benzidine with a pigment coupling agent, preferably an acetoacetarylamide, and incorporating in the pigment a water-soluble coupled diarylide dyestuff, preferably prior to the isolation and drying of the pigment, and the diarylide pigment composition having better colour strength and transparency properties than conventional diarylide pigments when incorporated in printing inks.
Abstract:
PREPARATION OF STORAGE-STABLE AQUEOUS SOLUTIONS CONTAINING 10-25 WEIGHT PRECENT OF A DISAZO J ACID UREA DYE BY COUPLING AN ARYL DIAZONIUM SALT, FOR EXAMPLE, A SALT FROM BROENNER''S ACID, AND J ACID UREA, AT A MOLAR RATIO OF ABOUT 2:1, IN AN AQUEOUS MEDIUM, AT A PH OF ABOUT 3-9, AT A TEMPERATURE OF ABOUT 0-65*C., IN THE PRESENCE OF TRIETHANOLAMINE AS THE ACID ACCEPTOR.