Abstract:
A process of dyeing polyamide-containing material is disclosed using dyes of the following formula: ##STR1## wherein Me is cobalt or chromium,Ka.sup..sym. is a cation,p is 0 or 1,R and R' are each independently of the other hydrogen or a group of the formula --CO--(O).sub.n --Y, wheren is 0 or 1, andY is C.sub.1 -C.sub.5 alkyl, or phenyl which may be substituted by nitro, halogen, C.sub.1 -C.sub.5 alkyl or C.sub.1 -C.sub.5 alkoxy, with the proviso that R and R' may not both be hydrogen if p is 1.Novel dyes within this class are also disclosed. The process is especially useful for dyeing leather.
Abstract:
Chrome azo-azomethine dyes are disclosed which contain a benzthiazolylphenyl or stilbenyl radical bound via an aldehyde group to the aldehyde moiety of the azomethine dyes. The dyes are particularly useful for dyeing wool, polyamide and leather.
Abstract:
The novel asymmetric 1:2 chrome complex dyes of the formula I given in claim 1 are suitable in particular for dyeing wool or polyamide and especially leather.
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:
Asymmetrical 1:2-chromium complex dyestuffs having excellent fastness to light, rubbing, washing, alkali, milling sea water, decatizing and perspiration and having the formula ##STR1## WHEREIN A.sub.1 represents o-phenylene unsubstituted or substituted by halogen, nitro, lower alkyl, lower alkylsulphonyl, phenylsulphonyl, --SO.sub.3.sup.- M.sup.+ or ##STR2## wherein R.sub.1 represents hydrogen, lower alkyl and R.sub.2 represents hydrogen, lower alkyl or phenyl, or by a cellulosic fiber-reactive group, or o-naphthylene unsubstituted or substituted by --SO.sub.3.sup.- M.sup.+,A.sub.2 represents unsubstituted o-phenylene or o-naphthylene unsubstituted or substituted by hydroxyl or --SO.sub.3.sup.- M.sup.+, andA.sub.3 represents o-phenylene unsubstituted or substituted by halogen, nitro, lower alkyl, lower alkoxy, lower alkylsulphonyl, phenylsulphonyl, --SO.sub.3.sup.- M.sup.+ --or ##STR3## wherein R.sub.3 and R.sub.4 independently of each other represent hydrogen or lower alkyl, or o-naphthylene unsubstituted or substituted by nitro, --SO.sub.3.sup.- M.sup.+ or bothB represents 1,2-naphthylene unsubstituted or substituted by halogen, phenylamino, --COO.sup.- M.sup.+, --SO.sub.3.sup.- M.sup.+, N-lower-alkyl-sulphamoyl or N,N-di-lower-alkylsulphamoyl; 4-(1-phenyl-3-methyl-pyrazol-5-onyl), 4-(halogenphenyl-, 1-lower-alkylsulphonylphenyl- or 1-SO.sub.3.sup.- M.sup.+ -phenyl-3-methyl-pyrazol-5-onyl) or 4-(1-SO.sub.3.sup.- M.sup.+ -phenyl-3-methyl-5-amino-pyrazolyl),M.sup.+ represents a colorless cation, andn represents an integer from 1 to 3,And wherein ring G is unsubstituted or substituted by halogen, --SO.sub.3.sup.- M.sup.+ - or sulphamoyl,X.sub.1 represents --O--,X.sub.2 represents --O-- or --COO--,X.sub.3 represents --O--, --COO-- or ##STR4## wherein R denotes lower alkyl or phenyl X.sub.4 represents --O--, --NH-- or ##STR5## wherein R has the meaning given in the definition of X.sub.3, and ##STR6## being linked to A.sub.1, A.sub.3 or both and the dyestuff molecule having, in all, from 0 to 3 --SO.sub.3.sup.- M.sup.+ groups, andwherein more than one ##STR7## group is present it is not bound to the same ring A.sub.1, A.sub.3 or B and when A.sub.1, A.sub.3 or B are unsubstituted or substituted o-phenylene, the ##STR8## group is bound thereto in the para position with respect to the substituent participating in the chromium complex.
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:
1:2 Chromium complex dyes of the formula ##SPC1##Wherein A represents the radical of a diazo component, B represents the radical of a coupling component, --X-- is --O--, --NH--, ##EQU1## --Y-- is --O-- or --COO--, R.sub.1 is hydrogen or alkyl and R.sub.2 is a radical of the benzene or naphthalene class which is substituted by a carboxy or a sulpho group, K.sup.+ represents a cation, and wherein the benzene ring b can carry a further fused benzene ring or can be substituted by halogen, nitro, low molecular alkyl or alkoxy as well as arylazo groups, and the radicals A and B are devoid of --SO.sub.3 H and --COOH groups. These dyes are useful for dyeing and printing natural and synthetic polyamides to produce level dyeings of good fastness, especially fastness to pulling, water and perspiration.
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.