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序号	专利名	申请号	申请日	公开（公告）号	公开（公告）日	发明人
101	Production of 4:4'-diamino-1:1'-dianthraquinonyl sulfonic acids	US10587661	1961-04-27	US3234242A	1966-02-08	MAX JOST; WALTER KERN; MAURICE GRELAT

102	High molecular organic products colored with a pigment dyestuff	US31085063	1963-09-23	US3228780A	1966-01-11	MAURICE GRELAT

103	2-bromo-1, 4-diamino-5-or 8-nitroanthraquinone	US21216362	1962-07-24	US3215711A	1965-11-02	OTTO FUCHS; HEINZ RENTEL

104	Process of dyeing polyester fibers with diamino-anthraquinone-carbonitrile dyestuffs	US29649363	1963-07-22	US3203751A	1965-08-31	DAVID HILDRETH JOHN

105	Production of 1, 3, 4-oxdiazoles	US79907559	1959-03-13	US3065238A	1962-11-20	HANS WEIDINGER; JOACHIM KRANZ

106	New heterocyclic orthoquinones	US7228560	1960-11-29	US3047575A	1962-07-31	BOYLE RICHARD J; BIRSTEN OSCAR G; MOSBY WILLIAM L

107	1, 4-diamino-2, 3-anthraquinonedicarboxamides	US26008551	1951-12-05	US2692272A	1954-10-19	PERKINS MELVIN A

108	Compounds of the oxdiazole series	US77443647	1947-09-16	US2464831A	1949-03-22	STILMAR FREDERIC B

109	Compounds of the anthraquinone series	US46324842	1942-10-24	US2353010A	1944-07-04	BUXBAUM EDWIN C

110	Dyestuff for artificial silk and process of making the same	US56747031	1931-10-07	US1939593A	1933-12-12	LEE HENRY R; BUXBAUM EDWIN C

111	Process for preparing beta-amino-anthraquinones	US46104330	1930-06-13	US1910692A	1933-05-23	IVAN GUBELMANN; TINKER JOHN M

112	Production of anthraquinone derivatives	US24145027	1927-12-20	US1862786A	1932-06-14	EDWARD DRESCHER HUGH ALBERT; WILLIAM SMITH; JOHN THOMAS

113	2-amino-7-chloro-anthraquinone and process of making the same	US20326327	1927-07-02	US1810012A	1931-06-16	IVAN GUBELMANN; WEILAND HENRY J; OTTO STALLMANN

114	Process of preparing alpha-aminoanthraquinone-beta-carboxylic acids	US17255627	1927-03-03	US1698900A	1929-01-15	KARL WILKE

115	Production of alpha-amino anthraquinones	US48624921	1921-07-20	US1657420A	1928-01-24	JOHN THOMAS; HUGH DAVIES ARTHUR

116	Ink set and thermal transfer recording sheet	US15130695	2016-04-15	US09701146B2	2017-07-11	Koromo Shirota; Taichi Shintou; Masao Nakano
An ink set contains a first ink containing a compound in which a pyrazolone ring and a thiazole ring are bonded and a second ink containing a compound in which a pyrazolone ring and a pyridinedione ring are bonded. A thermal transfer recording sheet has a first ink layer containing a compound in which a pyrazolone ring and a thiazole ring are bonded and a second ink layer containing a compound in which a pyrazolone ring and a pyridinedione ring are bonded.
117	Fluorescent quinacridone pigments	US319399	1994-10-06	US5561232A	1996-10-01	Zhimin Hao; John S. Zambounis; Abul Iqbal
Compounds of formulaA(B).sub.x, (I),whereinx is an integer from 1 to 4,A is the radical of a chromophore of the quinacridone, anthraquinone, perylene, indigo, quinophthalone, isoindolinone, isoindoline, dioxazine, phthalocyanine or azo series, which radical contains x N-atoms attached to B, preferably with at least one directly adjacent or conjugated carbonyl group,B is a group of formula ##STR1## and, if x is 2, 3 or 4, may also be one, two or three hydrogen atoms. The symbols Q, R.sub.1, R.sub.2, R.sub.3, R.sub.4, X, Y, Z, m and n, are as defined in claim 1. These carbamate group-containing soluble chromophores am distinguished by outstanding solid state fluorescence in the UV range as well as the by ease with which they can be converted to the corresponding pigments in the substrate in which they are incorporated.
118	Process for producing 4,4'-diamino-1,1,'-dianthraquinonyl pigments	US921574	1992-07-30	US5320678A	1994-06-14	Hiroki Inoue; Toshiaki Kishimoto; Iwao Sakaguchi; Kunitoshi Takahashi; Yoshiaki Hayashi; Keisuke Ito
A desulfonation reaction mixture of 4,4'-diamino-1,1'-dianthraquinonyl-3,3'-disulfonic acid obtainable in a conventional manner is mixed in the form of an aqueous acid suspension with a surface active agent, followed by filtration, whereby filterability and flowability of the produced 4,4'-diamino-1,1'-dianthraquinonyl pigment are efficiently improved.
119	Anthraquinone vat dyes	US5991	1987-01-21	US5028709A	1991-07-02	Jean-Marie Adam
The invention relates to vat dyes of the formula ##STR1## wherein [A] and [A'] and X are as defined in claim 1. The vat dyes of formula I are suitable for dyeing or printing a wide range of materials. Dyeings with good fastness properties are obtained in particular on cellulose material.
120	Process for the preparation of 1-aminoanthraquinones	US110162	1987-10-19	US4770818A	1988-09-13	Eric Plattner; Gottfried Seifert; Tibor Somlo
There is disclosed a process for the preparation of 1-aminoanthraquinones from 5-nitro-1,4,4a,9a-tetrahydroanthraquinones with a basic reducing agent, which process is carried out under pressure in the temperature range above 100.degree. C. and in an aqueous-organic medium. The process affords very pure 1-aminoanthraquinone, which is, inter alia, an important intermediate.

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