Abstract:
A process for the continuous preparation of imidoperoxycarboxylic acids of the formula ##STR1## in which A is C.sub.2 -C.sub.4 -alkylene, phenylene, naphthylene or a group of the formula ##STR2## and R is a group of the formula --COOH, --SO.sub.3 H or --Cl, and X is C.sub.1 -C.sub.19 -alkylene or arylene, in which a solution of imidocarboxylic acids of the formula ##STR3## in sulfuric acid or methanesulfonic acid and an aqueous solution of hydrogen peroxide are continuously metered into a static mixer, then the solution of the imidoperoxycarboxylic acid obtained in this way is treated with water and the precipitated product is isolated.
Abstract:
Triphendioxazine compounds, which are suitable as fiber-reactive dyestuffs, of the general formula (1) ##STR1## in which R.sup.1 and R.sup.2 are each a hydrogen atom, an optionally substituted alkyl group with 1 to 8 carbon atoms, the substituents being, for example, sulfo, sulfato, carboxy and optionally substituted alkylamino and dialkylamino groups, or a cycloalkyl group which can optionally be substituted by methyl and/or amino, alkanoylamino or benzoylamino, or an optionally substituted phenyl radical, the substituents of which are, for example, sulfo, carboxy, halogen, alkyl with 1 to 4 carbon atoms, alkoxy with 1 to 4 carbon atoms, nitro and .beta.-sulfatoethylsulfonyl, or a naphthyl radical which can be substituted by 1, 2 or 3 sulfo groups and/or a fiber-reactive group of the vinylsulfone series, or in which R.sup.1 and R.sup.2, together with the nitrogen atom, can form a heterocyclic radical, and in which the benzene nuclei A can be substituted by 1 or 2 substituents from the group comprising alkyl with 1 to 6 carbon atoms, alkoxy with 1 to 5 carbon atoms, halogen, carboxyl and sulfo, the two radicals X.sup.1 and X.sup.2 are identical to one another or different from one another and are a hydrogen atom, a halogen atom, a cycloalkyl group, an aralkoxy group, an alkoxy group, an aryloxy group, an alkyl group, an aryl group, an aralkyl group or a cyano, carboxy, carbalkoxy, mono- or di-alkylcarbamoyl, arylarylcarbamoyl, alkanoylamino or aroylamino group, and Y represents the vinyl group or ethyl group which contains, in the .beta.-position, a substituent which can be eliminated by an alkali, or is the .beta.-hydroxyethyl group, and M represents a hydrogen atom or an alkali metal or the equivalent of an alkaline earth metal, and the compound (1) contains at least one sulfo or sulfato group.The compounds (1) are used for dyeing material containing hydroxy and/or carboxamide groups, in particular fiber material, such as cellulose fiber material and wool, on which they give deep blue dyeings.
Abstract:
New compounds had been found which correspond to the formula ##STR1## as well as processes for preparing them by sulfonation of 3.beta.-sulfato- or 3-.beta.-hydroxyethylsulfonyl - aminobenzene. The novel compounds are valuable intermediary products for the preparation of azo fibre-reactive dyestuffs which have very good dyeing properties and a high fibre-reactivity yielding dyeings of excellent fastnesses, especially to light and wet processing.
Abstract:
Water-soluble disazodyestuffs of the formula ##STR1## in which R.sub.1 and R.sub.2 are identical or different and each is hydrogen, methyl, ethyl or methoxy, and R.sub.3 is hydrogen, chlorine, nitro or alkyl of 1 to 4 carbon atoms, and their salts have been found which possess very good dyeing characteristics and are very well suitable for dyeing of synthetic polyamides and yield dyeings on these fibers with good to very good wet fastnesses and fastnesses to processing and to use. In accordance with this, an improved process had been found for coloring synthetic polyamide fibres by applying the above dyestuffs of the invention on said fibres in usual dyeing and printing methods and fixing them on the fibre by methods as usual in the art.
Abstract:
Fiber-reactive azo dyestuffs are obtained by diazotizing an amine of the formula ##STR1## in which Z stands for--CH.sub.2 -CH.sub.2 --A or--CH.dbd.CH.sub.2in which A is N,N-dialkylamino with 1 to 4 carbon atoms in each alkyl moiety or is chlorine, bromine, sulfato, thiosulfato, phosphato and acetoxy it with an azo component of the formulaH--B,in which B is ##STR2## wherein R is hydrogen, alkyl with 1 to 4 carbon atoms, alkoxy with 1 to 4 carbon atoms, acetylamino, chlorine or bromine, R.sub.1 is hydrogen or alkyl with 1 to 4 carbon atoms unsubstituted or substituted by hydroxy or cyano, and R.sub.2 is lower alkyl with 1 to 4 carbon atoms unsubstituted or substituted by hydroxy or cyano, or is acetyl or benozyl. The new dyestuffs are especially suitable for dyeing and printing fiber materials, such as silk, wool, synthetic polyamide or polyurethane, and above all, native and regenerative cellulose. They possess a very high fiber reactivity so that they fix on the fiber material very rapidly even at low temperatures and are thus very suitable in continuous dyeing processes.
Abstract:
Fiber-reactive azo dyestuffs are obtained by diazotizng an amine of the formula ##STR1## in which Z stands for--CH.sub.2 --CH.sub.2 --A or--CH.dbd.CH.sub.2in which A is N,N-dialkylamino with 1 to 4 carbon atoms in each alkyl moiety or is the radical of a mono- or poly-basic acid capable of being split off by an alkaline agent and coupling it with an azo component of the formulaH-B,in which B is aniline, naphthol, naphthylamine, aminonaphthol, pyridone, aminopyridine, 1-phenyl-4-aminopyrazole or 1-phenyl-5-pyrazolone, unsubstituted or substituted on the aromatic and/or heterocyclic moieties by one to four groups selected from alkyl, alkoxy, oxalkyl, cyanoalkyl, aminoalkyl or alkoxyalkyl with 1 to 6 carbon atoms in each alkyl and alkoxy moiety, chlorine and bromine, sulfonic acid, vinylsulfonyl, carboxyl, acylamino and arylamino groups.
Abstract:
Dyestuffs of the formula (1) ##SPC1##Wherein A is an optionally substituted radical of the benzene or naphthalene series which, however, does not contain a sulfonic acid group, B is the radical of a coupling component of the benzene, naphthalene, pyrazolone, aminopyrazole, hydroxyquinoline or aceto-acetyl-arylamide series, which, however, does not contain a sulfonic acid group, and R is hydrogen or the lower alkyl.These dyestuffs are very well water-soluble in spite of having a high molecular weight and containing only one sulfonic acid group. They are especially suitable for dyeing or printing materials of natural and synthetic nitrogen-containing fibers, such as wool, silk, polyamide or polyurethane fibers, preferably if dyed from an acid to neutral dye bath. They show a very good colour buildup and migration power when being applied on the material mentioned which allows to obtain even dyeings of good fastnesses to light and to wet processing, for example, to washing and to perspiration.
Abstract:
Water-soluble disazo compounds of the formula (1) ##STR1## and diamino compounds serving as starting compounds (tetrazo components), of the formula (4) ##STR2## in which the formulae moieties occurring twice, namely Z, K and X, in each case have a meaning identical to one another and the groups Z are bonded to the two benzene nuclei in each case in the ortho- or in each case in the para-position relative to the ethylenedioxy substituent, and the azo groups or amino groups and the groups Z in the benzene nuclei are in each case bonded in the meta-position relative to one another and K is the radical of a coupling component containing a sulfato, carboxy or sulfo group, X denotes a hydrogen atom or a fiber-reactive group and Z is a group of the formula --SO.sub.2 --CH.dbd.CH.sub.2 or --SO.sub.2 --CH.sub.2 --CH.sub.2 --Y in which Y denotes a radical which can be eliminated in aqueous medium under alkaline or acidic conditions or the hydroxy group.Disazo compounds of the formula (1) can be used as dyestuffs having fiber-reactive properties for dyeing, for example, cellulose fiber material and wool and be prepared by tetrazotizing diamines of the formula (4) and coupling with coupling components evident from the formula (1).Diamino compounds of the formula (4) are obtained by acetylating a 1,2-di-(o- or p-aminophenoxy)-ethane, chlorosulfonating this bis-acetylamino compound and reducing the sulfonyl chloride groups to sulfinic acid groups, which are then oxyethylated to give .beta.-hydroxyethylsulfonyl groups, which, after deacetylation of acetylamino groups, can be converted in a manner which is in itself known into one of the abovementioned groups Z, for example into the .beta.-sulfatoethylsulfonyl group by means of a sulfating agent.
Abstract:
Novel, valuable unsymmetrical 1:2-cobalt complex dyestuffs of an azo compound and an azomethine compound have been found which are well suited for the dyeing of natural and synthetic polyamide fibres, yielding even dyeings of high fastnesses to wet processing and use as well as to light. The novel dyestuffs can be prepared either by cobalting the equimolar mixture of the metalfree azo and azomethine dyestuffs with a cobalt-yielding compound at a pH of 5 to 10 at 60 .degree. to 150.degree. C., or by first cobalting the azomethine compound and then reacting it with the equimolar amount of the metalfree azo compound. The compounds are 1:2-cobalt complex compounds of the compounds ##STR1## in which R.sub.1 is chlorine, lower alkyl or nitro, R.sub.2 is hydrogen, lower alkyl or lower alkoxy, R.sub.3 is hydrogen, chlorine, nitro or lower alkyl, Z is ##STR2## in which R.sub.4 is hydrogen, lower alkyl or lowr alkoxy, R.sub.5 is hydrogen, lower alkyl or lower alkoxy, X is hydroxy, sulfoalkyl of from 1 to 4 carbon atoms, or ##STR3## R.sub.9 is hydrogen or lower alkyl, and R.sub.6 and R.sub.7 are different from each other and each is nitro or sulfo.
Abstract:
Process for the level dyeing of wool, having an anti-felting finish consisting of a coating layer of polyimine or polyamine resin, with reactive dyestuffs, which is carried out according to a graduated temperature exhaustion method from an aqueous liquor using one or several reactive dyestuffs of the formulae ##SPC1##In which F stands for a dyestuff radical having at least 2 sulfonic acid groups linked to an aromatic radical of the chromophore, Z stands for a reactive group of the vinylsulfone, vinylsulfonamide or acrylamide type, n is 1 or 2, and R and R.sub.1 each stands for hydrogen atoms or lower alkyl radicals, in the absence of adjuvants and/or without any pretreatment of the material to be dyed.