Abstract:
Novel dyestuffs have been found which are obtainable by reactingA) polyamines containing at least 2 primary or secondary amino groups withB) reactive compounds containing at least two groups which are reactive towards primary and secondary amines in an amount of 5 to 95 mol %, relative to the primary and secondary amino groups of the polyamine, andC) dyestuffs containing at least one acylatable primary or secondary amino group in an amount of 10 to 200 mol %, relative to the reactive compound, andD) carbonyl- or sulphonyl-containing acylating agents in an amount of 5 to 95 mol %, relative to the primary and secondary amino groups of the polyamineand can be used in particular for coloring and printing cellulose-/amido-containing materials and as recording fluids for ink- jet recording systems.
Abstract:
Novel tris-azo dyes and a liquid crystal composition containing the tris-azo dyes. The tris-azo dyes are of the general formula: ##STR1## wherein R.sub.1 and R.sub.2 are various aromatic groups including aromatic amines, substituted aromatic amines, hydroxy-substituted aromatic groups and substituted hydroxy-containing aromatic groups. When the tris-azo dichroic dyes are used as a guest dye in a host liquid crystal material, they form a novel liquid crystal composition for use in liquid crystal displays.
Abstract:
To provide a dye for an anisotropic dye film to be formed by a wet system film-forming method, which is black and which has a high degree of polarization and a high degree of molecular orientation an anisotropic dye film using the dye, and the like. A trisazo dye for an anisotropic dye film to be formed by a wet system film-forming method, of which the free acid form is represented by the following formula (1), a dye composition for an anisotropic dye film containing the dye, an anisotropic dye film, and a polarizing element using the anisotropic dye film: wherein A1 is a phenyl group or aromatic heterocyclic group which may have a substituent, B1 is an aromatic hydrocarbon group which may have a substituent, D1 is an aromatic hydrocarbon group or aromatic heterocyclic group which may have a substituent, R1 is a hydrogen atom, a hydroxyl group or an amino group which may have a substituent, and each of m and n is 0 or 1.
Abstract:
Trisazo dyes of the formula ##STR1## where R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are identical or different and each, independently of the others, is hydrogen, methyl, ethyl, methoxy or chlorine, R.sup.5 is C.sub.2 -C.sub.4 -alkyl, X is C.sub.1 -C.sub.24 -mono- or dialkylamino, monobenzylamino, mono-(phenyl-ethyl)-amino, monophenylamino, N-(C.sub.1 -C.sub.12 -alkyl)-N-benzylamino, N-(C.sub.1 -C.sub.12 -alkyl)-N-(phenylethyl)amino or N-(C.sub.1 -C.sub.12 -alkyl)-N-phenylamino or each of the phenyls substituted by C.sub.1 -C.sub.12 -alkyl, cyclo-hexyl, 4-(C.sub.1 -C.sub.12 -alkyl)cyclohexyl, C.sub.1 -C.sub.24 -alkyloxy, phenoxy or C.sub.1 -C.sub.24 -alkanoyloxyl, or is OR, where R is C.sub.1 -C.sub.24 -alkyl, unsubstituted or C.sub.1 -C.sub.12 -alkyl-, cyclohexyl-, 4-(C.sub.1 -C.sub.12 -alkyl)cyclohexyl-, C.sub.1 -C.sub.24 -alkoxy-, phenoxy- or C.sub.1 -C.sub.24 -alkanoyl-oxy-substituted benzyl or phenylethyl, and A is a radical of the formula ##STR2## where R and X each have the above-mentioned meanings, and R.sup.6 is hydrogen or C.sub.1 -C.sub.14 -alkyl, R.sup.7 is hydrogen, methyl, ethyl, methoxy or chlorine, R.sup.8 is hydrogen, methyl, hydroxy or C.sub.1 -C.sub.8 -alkoxy and R.sup.9 is hydrogen or methyl, or the rings B, or B and C being benzofused, are used in liquid crystalline media and for dyeing synthetic polymers.
Abstract:
Black trisazo dyes for cellulosic textiles, leather and especially paper having the structure ##STR1## where A is ##STR2## one of B.sub.1 and B.sub.2 is hydrogen and the other is --SO.sub.3 M or a mixture thereof, and M is hydrogen, sodium, potassium, lithium or --HNR.sub.1 R.sub.2 R.sub.3 wherein R.sub.1, R.sub.2 and R.sub.3 represent the same or different substituents selected from hydrogen, lower alkyl and lower hydroxyalkyl, and stable liquid concentrates of these dyes are described.