Abstract:
This disclosure describes a novel process for liberating the free bases of certain 1,4-di[.omega.-(2-hydroxyethylamino)alkylamino]anthraquinones from the salts thereof.
Abstract:
1-Amino-2-phenoxy-4-hydroxyanthraquinones, which are useful as a red disperse dye for polyester fibers, and also useful as an intermediate for the production of other red disperse dyes, are produced in a high yield and purity by reacting a 1-amino-2-halogeno-4-hydroxyanthraquinone with a phenol compound in a sulfane solvent in the presence of an acid binding agent.
Abstract:
Dye mixtures containing at least two dyes of the formula (1) ##STR1## wherein R is hydrogen, methyl or ethyl, and n is an integer from 2 to 4, exhibit on synthetic textile material a build-up which is considerably better than that of the individual dyes.
Abstract:
1-Hydroxy-4-amino-5- or -8-nitroanthraquinone is obtained in high yields and in high purity when 1,8-dinitroanthraquinone or 1,5-dinitroanthraquinone respectively is reacted below 80.degree. C. in oleum in the presence of boric acid with reducing agents. The products of the process are valuable polyester dyestuffs as well as dyestuff intermediate products.
Abstract:
Anils of 1,4- and 1,8-diaminoanthraquinone with p-alkyl- and p-alkoxybenzaldehyde are found to be pleochroic dyes which form guest-host combinations with dielectrically positive anisotropic nematic liquid crystals. These combinations are of value in electro-optical display devices.
Abstract:
The invention relates to mixtures of water-insoluble anthraquinone dyestuffs of the formula ##STR1## in which A and B are amino or hydroxylR is alkyleneX is a direct bond, oxygen, sulphur or iminoAr is arylD.sub.1 and D.sub.2 are hydrogen or halogen,Hal represents chlorine or preferably bromine andn represents on average a number from 0.1 to 2.5.The preferred variant for the preparation of the dyestuffs (wherein Hal represents bromine) is characterized in that anthraquinone compounds of the formula ##STR2## are brominated on the aryl radical Ar. The dyestuffs are outstanding suitable for the dyeing of polyester fibers.
Abstract:
A (7S,9S) isomer or its racemic modification of the aminonaphthacene derivative of the formula: ##STR1## wherein R.sup.1 is a hydrogen atom, a hydroxyl group or a lower alkoxy group, R.sup.2 is a hydrogen atom or a hydroxyl group, R.sup.3 and R.sup.4 are each a lower alkoxy group or, when taken together, represent an ethylenedioxy group or an oxo group, A is an ethylene group optionally bearing at least one lower alkyl and Q is a hydroxyl group, a lower alkoxy group or a dimethylamino group, or an acid addition salt thereof, which is useful as an anti-tumor agent.
Abstract translation:A(7S,9S)异构体或其下式的氨基并四苯衍生物的外消旋改性:其中R1是氢原子,羟基或低级烷氧基,R2是氢原子或羟基,R3和 R 4各自为低级烷氧基,或者一起表示亚乙二氧基或氧代基时,A为任选具有至少一个低级烷基并且Q为羟基,低级烷氧基或二甲基氨基的亚乙基, 或其酸加成盐,其可用作抗肿瘤剂。
Abstract:
This disclosure describes 1-(aminoalkylamino)-5,8-dihydroxy-4-substituted-anthraquinones useful as chelating agents and for inhibiting the growth of transplanted mouse tumors.
Abstract:
This disclosure describes 1,4-bis(guanidinylamino)-5,8-dihydroxyanthraquinones useful as chelating agents and for inhibiting the growth of transplanted mouse tumors.
Abstract:
Dyestuffs, which are free from nitro groups and sulphonic acid groups, of the formulaF--Z--(OA).sub.n --OR IwhereinF denotes an anthraquinone nucleus which contains at least one auxochromic group in the .alpha.-position,Z denotes a direct bond or a bridge member,A denotes alkylene,R denotes alkyl, aralkyl, cycloalkyl, aryl or acyl andn denotes 3 to 8,with the proviso that R does not represent aralkyl if n denotes the number 3 and the number of the auxochromic groups is two, have a melting point below 140.degree. C., in particular below 100.degree. C., and are outstandingly suitable for dyeing and printing synthetic fibre materials, in particular those of polyesters, on which they produce dyeings with good fastness to sublimation, washing and light.The dyestuffs are advantageously employed in the form of liquid or pulverulent preparations which contain, in addition to the dyestuff, emulsifying polar/non-polar compounds and, if appropriate, formulating agents and extenders.These preparations are distinguished by very high solubility in cold water and require no further dyeing auxiliaries such as, for example, carriers.