Abstract:
Azo pigments of the Beta -hydroxynaphthoic acid series containing an o-phenylenediamine and a trimellitic acid imide moiety. These pigments are best illustrated by the formula
The pigments are suitable for example for coloring resins, surface coatings and printing inks and give brilliant hues of very good fastness properties.
Abstract:
Metal-containing azomethine pigment dyes derived from 1 mole of an o-phenylenediamine and 2 moles of a Beta hydroxynaphthaldehyde which are useful for coloring printing inks, surface coatings, resins and the like.
Abstract:
PCT No. PCT/EP94/02637 Sec. 371 Date Feb. 12, 1996 Sec. 102(e) Date Feb. 12, 1996 PCT Filed Aug. 9, 1994 PCT Pub. No. WO95/05421 PCT Pub. Date Feb. 23, 1995Leucoindigo preparations in granule form consisting essentially of leucoindigo and alkali metal hydroxide and production of these preparations and use thereof for dyeing cellulose-containing textile material.
Abstract:
PCT No. PCT/EP94/02637 Sec. 371 Date Feb. 12, 1996 Sec. 102(e) Date Feb. 12, 1996 PCT Filed Aug. 9, 1994 PCT Pub. No. WO95/05421 PCT Pub. Date Feb. 23, 1995Leucoindigo preparations in granule form consisting essentially of leucoindigo and alkali metal hydroxide and production of these preparations and use thereof for dyeing cellulose-containing textile material.
Abstract:
A process for the preparation of 2,4-dichloro- or 2-methyl-4-chlorophenoxyacetic acid or alpha -2,4-dichloro- or alpha -2-methyl-4-chlorophenoxypropionic acid by reacting phenoxyacetic or 2-methylphenoxyacetic acid or alpha -phenoxypropionic or alpha -2-methylphenoxypropionic acid with chlorine in water, wherein phenoxyacetic acid or phenoxypropionic acid is precipitated from an aqueous solution thereof, chlorine gas is passed into the resulting suspension of phenoxyacetic or 2-methylphenoxyacetic acid or alpha -phenoxypropionic or alpha -2-methylphenoxypropionic acid in water at from 30 DEG to 70 DEG C. at a rate not exceeding the rate at which it is consumed in the suspension, until from 100 to 110% of the theoretically required amount of chlorine gas has been taken up by the suspension, and the 2,4-dichloro- or 2-methyl-4-chloro-phenoxyacetic acid or alpha -2,4-dichloro- or alpha -2-methyl-4-chloro-phenoxypropionic acid is isolated from the suspension.
Abstract:
A process for the preparation of 2,4-dichloro- or 2-methyl-4-chlorophenoxyacetic acid or alpha -2,4-dichloro- or alpha -2-methyl-4-chlorophenoxypropionic acid by reacting phenoxyacetic or 2-methylphenoxyacetic acid or alpha -phenoxypropionic or alpha -2-methylphenoxypropionic acid with chlorine in water, wherein phenoxyacetic acid or phenoxypropionic acid is precipitated from an aqueous solution thereof, chlorine gas is passed into the resulting suspension of phenoxyacetic or 2-methylphenoxyacetic acid or alpha -phenoxypropionic or alpha -2-methylphenoxypropionic acid in water at from 30 DEG to 70 DEG C. at a rate not exceeding the rate at which it is consumed in the suspension, until from 100 to 110% of the theoretically required amount of chlorine gas has been taken up by the suspension, and the 2,4-dichloro- or 2-methyl-4-chloro-phenoxyacetic acid or alpha -2,4-dichloro- or alpha -2-methyl-4-chloro-phenoxypropionic acid is isolated from the suspension.
Abstract:
PCT No. PCT/EP94/02637 Sec. 371 Date Feb. 12, 1996 Sec. 102(e) Date Feb. 12, 1996 PCT Filed Aug. 9, 1994 PCT Pub. No. WO95/05421 PCT Pub. Date Feb. 23, 1995Leucoindigo preparations in granule form consisting essentially of leucoindigo and alkali metal hydroxide and production of these preparations and use thereof for dyeing cellulose-containing textile material.
Abstract:
A process for purifying indigo comprises extracting an aqueous leuco indigo alkali metal salt solution with an inert solvent, eg toluene under oxygen-excluding conditions and conventionally regenerating the indigo by oxidation. The solution may be made by dissolving the as-synthesized indigo in water by reduction in the form of the alkali metal salt of its leuco form.