Abstract:
Chromium complex dyes are disclosed which have the formula ##STR1## wherein S.sub.1 represents a hydrogen or halogen atom, a nitro group, a sulpho group, an alkyl or alkoxy radical, an acylamino or arylazo group,S.sub.2 represents a hydrogen or halogen atom, a nitro group, a sulpho group, an alkyl or alkoxy radical,S.sub.3 represents a hydrogen atom, a nitro group or a halogen atom,P is 1 or 2,R represents a fluorochloropyrimidyl or fluorotriazinyl radical, a chloroacetyl, bromoacetyl, .alpha.-chloro- or .alpha.-bromoacryloyl radical or an .alpha.,.beta.-dichloro- or .alpha., .beta.-dibromopropionyl radical, andM.sup..sym. represents a cation.
Abstract:
Chromium complex dyes which, in the form of their free acid, have the formula ##STR1## wherein one X represents the sulphonic acid group and the other X represents the nitro group, Y is a sulfone or sulfonamide group and Z is an acyl group. The dyes are suitable for dyeing natural and synthetic polyamides to produce dyeings which are level and have good fastness to light, perspiration, fulling, decatizing and carbonizing.
Abstract:
1:2 Chromium complex dyes of an azo compound of the formula ##STR1## and an azomethine compound of the formula ##STR2## COMPLEXED TO A CHROMIUM ATOM, WHEREIN A is an ortho-phenylene or -- naphthylene diazo component radical; B is an ortho-phenylene or -- naphthylene coupling component radical; X is --O-- or --CO--O--; X' is --O--, --NH--, --N(lower alkyl)--, --N(aralkyl)-- or --N(aryl)--; R is an aliphatic radical; the benzene ring "a" is unsubstituted or substituted by a fused benzene ring, halo, nitro alkyl or alkoxy; the molecule containing 0-5 water solubilizing groups and optionally a group of the formula --N=N--Ar--N=N--Ar' and/or -N=N--Ar" wherein Ar, Ar' and Ar" represent an aromatic or carbocyclic radical.
Abstract:
Dyes which are 1:2-chromium complexes, containing one azo dye or azomethine dye and one disazo dye or trisazo dye. The dyes are suitable for dyeing wool, synthetic polyamides and leather.
Abstract:
The present invention relates to novel chromium complex dyes of the formula ##STR1## wherein Z is hydrogen, chloro, bromo, nitro, lower alkyl or acylamino;L is H.sub.2 O, ammonia, ethanol or ethanolamine;Y is --O--or --COO--;Y' is --O--, --NH--, --N(lower alkyl)-- or --N(phenyl)--;A is ortho-phenylene or ortho-naphthalene which are unsubstituted or substituted by chloro, bromo, cyano, nitro, lower alkyl, lower alkoxy, phenoxy, sulfonamido, substituted sulfonamido, substituted sulfonyl or acylamino; andB is ortho-naphthalene which is unsubstituted or substituted by chloro, acyl, acylamino, lower alkyl, lower alkoxy, sulfonamido, substituted sulfonamido or substituted sulfonyl;where "acyl" is lower alkanoyl, lower alkoxycarbonyl, loweralkylsulfonyl, benzoyl, chlorobenzoyl, methylbenzoyl, nitrobenzoyl, phenoxycarbonyl, phenylsulfonyl or p-methylsulfonyl; substituted sulfonamido and those substituted by lower alkyl, lower hydroxyalkyl, lower alkoxyalkyl, lower cyanoalkyl, cyclohexyl or benzyl; and substituted sulfonyl is lower alkylsulfonyl, lower alkylsulfonyl substituted by hydroxy, chloro or lower alkoxy, chlorophenylsulfonyl, methylphenylsulfonyl, nitrophenylsulfonyl, methoxyphenylsulfonyl, or benzylsulfonyl.These dyes are useful in dyeing and printing materials such as silk, leather, wool and synthetic polyamides with good exhaustion and yielding level dyeings of good fastness properties.
Abstract:
Cobalt and chromium complex dyes which contain, bonded to a metal atom, one molecule of each of the azo compounds of the formula ##STR1## wherein R is methyl or ethyl and the phenyl ring a is unsubstituted or substituted by 1 to 2 chlorine atoms, nd mixtures thereof with the symmetrical 1:2 cobalt or chromium complex dyes of the azo compounds of the formulae (1) and (2), said dyes being useful in the dyeing and printing of a variety of materials, especially nitrogen containing materials such as silk, leather, polyamides, polyurethanes and especially wool to obtain level dyes having good fastness to light, washing, water, hot water, fulling, decatizing and carbonizing.
Abstract:
1:2 Chromium complex dyes of the formula ##STR1## wherein A is the radical of a diazo component of the benzene or naphthalene class which carries the complex forming group X in ortho-position to the azo group, B is the radical of a coupling component which couples in ortho-position to the oxy group, D is the radical of an amine of the benzene or naphthalene class which carries the complex-forming group in ortho-position to the azo group, X is an oxygen atom or a --CO--O-- group, Ar is an aromatic carbocyclic radical. Ar' and A" are aromatic carbocyclic or heterocyclic radicals, q is an integer from 0 to 5, n is an integer from 1 to 3, m is an integer from 0 to 2 and p is 0 or 1, but the sum of n+m may be at most 3, and wherein the benzene ring can carry a further fused benzene ring or can be substituted by halogen, nitro, alkyl or alkoxy, and K.sup.+ is a cation. The water-insoluble dyes are useful in dyeing polyamide textile material and for coloring leather, oil vanishes, and paper as well as viscose, polyamide, cellulose ether and cellulose ester spinning compositions, and the water-soluble dyes are useful in dyeing leather, wool, silk, casein, polyamide and polyurethane fibers and furs; and the dyes possess good covering power and fastness properties.
Abstract:
A process is described for the manufacture of chromium complexes of metallizable dyes in the form of solid dyestuff powders of low salt to salt-free content, or of concentrated solutions of low salt or salt-free content in which a metallizable dye, or a mixture of metallizable dyes, in an organic solvent which is immiscible or sparingly miscible with water, or reacted with a chromium compound, in the course of which any water which is liberated is removed by azeotropic distillation, and the resulting chromium complex, provided it is a 1:1 complex, is then optionally reacted in the presence of a base with a further mol of a metallizable dye, or of a colorless, complexforming compound, then isolated from undissolved constituents, and the resulting dye solution of low salt or salt-free content is optionally concentrated or evaporated to dryness, whereby it is possible the manufacture of 1:1 or 1:2 chromium complexes without the handicap of effluent pollution, and to isolate the dyes without using salt. The dyes obtained are especially suitable for the manufacture of concentrated solutions without the necessity of having to increase the solubility by means of extenders.
Abstract:
Chromium complex dyes of the formula ##SPC1##Wherein one of the symbols X.sub.1, X.sub.2 and X.sub.3 is hydrogen and each of the others is hydrogen, a halogen atom, a nitro group, a methyl or a methoxy group, R is a phenyl radical which is optionally substituted by halogen, low molecular alkoxy, alkyl or nitro and Me.sup.+ is a cation are disclosed; said dyes being useful in dyeing synthetic and natural polyamides to produce dyeings which are level and have good fastness to light, washing, fulling, decatizing and carbonizing.
Abstract:
Novel chromium complex dyes are disclosed which have the formula ##STR1## wherein S.sub.1 represents a hydrogen or halogen atom, a nitro group, a sulpho group, an alkyl or alkoxy radical, an acylamino or arylazo group,S.sub.2 represents a hydrogen or halogen atom, a nitro group, a sulpho group, an alkyl or alkoxy radical,S.sub.3 represents a hydrogen atom, a nitro group or a halogen atom,P is 1 or 2,R represents a fluorochloropyrimidyl or fluorotriazinyl radical, a chloroacetyl, bromoacetyl, .alpha.-chloro- or .alpha.-bromoacryloyl radical or an .alpha.,.beta.-dichloro- or .alpha.,.beta.-dibromopropionyl radical, andK.sup..sym. represents a cation.