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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
1	染料迫位酮的新颖结晶形状	CN02108261.8	2002-03-28	CN1379064A	2002-11-13	S·米歇利斯; J·W·施塔维茨
本发明涉及新颖结晶形式的C.I.溶剂橙60,其在染料合成中有较高的时空产率,比较容易制备。
2	Manufacturing method of colored contact lenses	JP28875493	1993-10-25	JP3483601B2	2004-01-06	ジェームス・ディー・フォード; フランク・エフ・モロック

3		JP838570	1970-01-31	JPS5220486B1	1977-06-03

4		JP15262984	1984-07-23	JPH0544471B2	1993-07-06	MIURA KONOE; OZAWA TETSUO; IWANAMI JUNKO

5	Anthraquinone compound and liquid crystal composition containing it	JP15262984	1984-07-23	JPS6130590A	1986-02-12	MIURA KONOE; OZAWA TETSUO; IWANAMI JUNKO
NEW MATERIAL:A compound shown by the formula I or formula II (R ¹ is H, alkyl, alkoxy, or halogen; R ² is H, alkyl, cycloalkyl, aryl, aralkyl, or tetrahydrofurfuryl). EXAMPLE: A compound shown by the formula III. USE: For a liquid crystal display element. Having improved solubility in and stability to liquid crystal. Having the maximum absorption at 700W900nm. PREPARATION: For example, an anthraquinone compound shown by the formula IVor V is reacted with a compound shown by the formula VI(e.g., 2-nitro- thiophenol, etc.) in the presence of an alkali in DMF. COPYRIGHT: (C)1986,JPO&Japio
6	PREPARATION OF COLORED CONTACT LENS	JP28875493	1993-10-25	JPH06235887A	1994-08-23	FURANKU EFU MOROTSUKU; JIEEMUSU DEII FUOODO
PURPOSE: To provide a process for producing a colored contact lens which does not require the immersion of the lens into an aq. soln. of dyes, for the purpose of coloring the lens to a desired color after polymerizing a hydrophilic monomer, the lens material. CONSTITUTION: The soft hydrogel contact lens is colored by uniformly dispersing the dyes into the lens. Water-soluble halotriazine dyes are used for the dyes. The dyes are brought into reaction with the hydrophilic monomer, in order to prepare the reactive dyes contg. just one functional group. The monomer is then polymerized in the soln. of the hydrophilic monomer homogeneously dispersed with the reactive dyes described above, under the conditions under which the hydrophilic polymer constituting the lens is formed. The dye is bonded to the polymer during the polymn.
7		JP1834670	1970-03-05	JPS4814645B1	1973-05-09

8	OLIGOMER MATERIAL	JP2000397420	2000-12-27	JP2002194003A	2002-07-10	TAKIMOTO HIROSHI
PROBLEM TO BE SOLVED: To obtain an oligomer material excellent in the coloring concentration, transparency, light resistance, weather (environmental gas) resistance, bleeding resistance and safety as coloring of a plastics member, electrophotographic toner, ink-jet recording, color filter or cosmetic. SOLUTION: This material has a recurring unit represented by formula (I) [wherein D is a color residue, ultraviolet-absorbing residue or antioxidant residue; X is a direct bond or a linking group; l is 0 or 1] and/or formula (II) [wherein A is an anionic color residue, ultraviolet-absorbing residue or antioxidant residue].
9	POLYCYCLIC VAT DYE	JP18586794	1994-08-08	JPH0762255A	1995-03-07	UDO BERUKUMAN; HARARUTO SHIYURIYUUTAA; MIHIYAERU SHIYUMITSUTO

10	PIPERAZINE ANTHRAQUINONE DYE FOR SYNTHETIC FIBER	JP847680	1980-01-28	JPS56104967A	1981-08-21	KITAO TEIJIROU; MATSUOKA MASARU
NEW MATERIAL:Piperazine anthraquinone dye of the formula I (where R is H or acyl group). EXAMPLE:1-Hydroxypiperazino[2,3,-C] anthraguinone. USE:A dye which is capable of dyeing a synthetic fiber, e.g., of polyester, polyamide, etc., in fast purple or blue color. PREPARATION:1-hydroxypiperazino[2,3-C] anthraquinone of the formula II (where the group corresponding to R of the formula I is H) is obtained by adding cupric chloride dihydrate and ethylene diamine to quinizarin and stirring the mixture. Also, a dye whose R (as shown in the formula I) is acyl group is obtained by adding acyl halide to a compound to the formula II and stirring the mixture.
11	METHOD OF MAKING SOLVENTTSOLUBLE DYESTUFF	JP14803677	1977-12-09	JPS5372037A	1978-06-27	KEISU NOOMAN PASUKINSU; DANKAN CHIYAARUZU RETSUDOMAN; IAN DEBITSUDO TAANAA

12	HETEROCYCLICAL CHROMOPHORE ARCHITECTURES	EP05817460	2005-10-26	EP1805144A4	2009-08-05	GOETZ FREDERICK J; GOETZ FREDERICK J JR
NLO chromophores of the form of Formula (I) and the acceptable salts, solvates and hydrates thereof, wherein Z, X<SUP>1-4</SUP>, p<SUP>1-2</SUP>, D and A have the definitions provided herein.
13	Anthraquinone dyestuffs	US51069365	1965-11-30	US3470178A	1969-09-30	NEEFF RUTGER; GOHRBANDT WILHELM; KUTH ROBERT

14	Process for producing dyestuffs of the anthraquinoneazine series	US32635063	1963-11-27	US3268532A	1966-08-23	WERNER ZERWECK; EMIL SCHWAMBERGER

15	Benzanthraquinoneacridine vat dyestuffs	US13576161	1961-09-05	US3134781A	1964-05-26	KLAUS WUNDERLICH; HANS-SAMUEL BIEN; FRITZ BAUMANN

16	Anthraquinone vat dyestuffs	US55679356	1956-01-03	US2807622A	1957-09-24	THEODOR HOLBRO; WALTER KERN

17	Vat dyestuff of the phthaloyl quinazoline series	US14219737	1937-05-12	US2187813A	1940-01-23	FRITZ BAUMANN; WERNER SCHWECHTEN HEINZ

18	Polycyclic vat dyes	US288310	1994-08-10	US5534627A	1996-07-09	Udo Bergmann; Harald Schlueter; Michael Schmitt
Polycyclic vat dyes of the general formula I ##STR1## where X is hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, halogen or nitro, obtainable by reacting (9)-benzo-5-aminoanthraquinonyl(2,1-h)-8-azapyrenone-3(II) ##STR2## with a benzoyl chloride of the formula III ##STR3## in a dipolar aprotic solvent.
19	Water-insoluble anthraquinone dyestuffs containing a halodiazinyl group which are soluble in aprotic solvents	US660403	1976-02-23	US4049661A	1977-09-20	Herbert Seiler; Paul Dussy
New reactive dyestuffs free from acid, salt-forming, water-solubilizing groups, and having the formula ##STR1## wherein D represents the radical of an anthraquinone dyestuff,Q represents NX.sub.3, O, S or NX.sub.3 CO wherein X.sub.3 represents hydrogen or lower alkyl,R represents diazinyl containing only chlorine, bromine or fluorine substituents, each of which can be split off as anion and which is bound to a ring carbon atom adjacent to a tertiary nitrogen atom,X.sub.1 represents hydrogen andX.sub.2 represents alkyl having from 8 to 18 carbon atoms, orX.sub.1 and X.sub.2 represents the same or different alkyl or alkoxyalkyl wherein X.sub.1 and X.sub.2 must together contain from 8 to 36 carbon atoms, orX.sub.1 represents cyclohexyl or cyclohexyl substituted by lower alkyl, andX.sub.2 represents alkyl of 1 to 18 carbon atoms, alkyl of 1 to 18 carbon atoms substituted by a member selected from the group consisting of hydroxyl, lower alkoxy, lower alkenyloxy and cyano, lower alkenyl, cyclohexyl or cyclohexyl substituted by lower alkyl, said dyestuffs being suitable for the dyeing and printing of hydrophobic organic fibre material, especially fibre material from synthetic polyamide, and being characterized by their good to excellent solubility in aprotic solvents or mixture of solvents.
20	Anthraquinone vat dyestuffs	US29949152	1952-07-17	US2840560A	1958-06-24	PAUL SUTTER

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