序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
141 Use of benzoquinones for the direct dyeing of keratin fibers LU83807 1981-12-02 LU83807A1 1983-09-01 LANG GERARD; MALAVAL ALAIN; GROLLIER JEAN FRANCOIS; ROSENBAUM GEORGES
142 USE OF BENZOQUINONES FOR THE DIRECT DYEING OF KERATIN FIBRES GB8234178 1982-12-01 GB2110722A 1983-06-22 LANG GERARD; MALAVAL ALAIN; GROLLIER JEAN-FRANCOIS; ROSENBAUM GEORGES
143 UTILISATION DE BENZOQUINONES POUR LA COLORATION DIRECTE DES FIBRES KERATINIQUES BE209630 1982-12-02 BE895224A 1983-06-02 LANG G; MALAVAL A; GROLLIER J-F; ROSENBAUM G
144 IT6840482 1982-12-01 IT8268404D0 1982-12-01 MALAVAL GERARD LANG ALAIN; GROLLIER JEAN FRANCOIS; ROSENBAUM GEORGES
145 CH1130576 1976-09-06 CH615952A5 1980-02-29 TSUJIMOTO MICHIHIRO; TSUKAHARA RYOICHI; NISHIZAWA TSUTOMU; OKUBO ICHIRO
146 IT2098875 1975-03-06 IT1033472B 1979-07-10 BORSOTTI G; RIBALDONE G
147 FR2345494B1 - FR7608873 1976-03-26 FR2345494B1 1978-11-03
148 PYRIMIDYL ANS S-TRIAZINYL DERIVATIVES GB1585276 1973-10-30 GB1451494A 1976-10-06
1451494 Pyrimidyl and s-triazinyl derivatives SANDOZ Ltd 30 Oct 1973 [3 Nov 1972 18 Dec 1972 12 Jan 1973] 15852/76 Divided out of 1451493 Heading C2C Novel pyrimidyl and s-triazinyl compounds of the formula in which R 4 11 signifies an unsubstituted alkyl, alkoxy, phenoxy or phenyl radical; an alkyl radical substituted by a chlorine or bromine atom or a hydroxy or alkoxy group; a phenyl radical substituted by up to three substituents selected from the group consisting of chlorine and bromine atoms, hydroxy and alkoxy groups; or a radical of formula in which each of R 30 and R 31 , which may be the same or different, signifies a hydrogen atom; an unsubstituted alkyl or phenyl radical; an alkyl radical substituted by a chlorine or bromine atom or a hydroxy or alkoxy group, preferably by a hydroxy group; a phenyl radical substituted by up to three substituents selected from the group consisting of chlorine and bromine atoms, hydroxy and alkoxy groups, preferably chlorine atoms and more preferably, such phenyl is mono-substituted; or a group of formula R-Y- or R1-Z- in which R signifies an unsubstituted alkyl or phenyl radical or an alkyl or phenyl radical substituted by chlorine, bromine, hydroxy or alkoxy, preferably an unsubstituted alkyl or phenyl radical, Y signifies a radical of formula -O-CO- or -SO 2 -, R1 signifies a hydrogen atom or has one of the significances of R, and Z signifies a radical of formula -CO-, -NR1CO- or -NR1SO 2 - in which R1 is as defined above, with the proviso that when one or R 30 or R 31 is a phenyl, substituted phenyl or a group of the formula R-Y- or R1-Z-, as defined above, the other has a significance other than phenyl, substituted phenyl, R-Y- or R1-Z, any alkoxy groups or alkyl or alkoxy moieties containing 1 to 4 carbon atoms. A signifies a radical of formula (a), (b), (c) or (d) in which each or R 5 , R 6 , R 17 , R 19 , R 20 and R 21 , which may be the same or different, signifies a hydrogen, fluorine, chlorine or bromine atom, a hydroxyl, alkyl, alkoxy, phenoxy or group, in which R 30 and R 31 are as defined above each of R 12 and R 13 , which may be the same or different, signifies a hydrogen atom, an alkoxy, phenoxy or group in which R 30 and R 31 are as defined above and each of R 15 and R 16 , which may be the same or different, signifies a fluorine, chlorine or bromine atom, a hydroxyl, alkyl, alkoxy, phenoxy or group, in which R 30 and R 31 are as defined above with the proviso that (i) when A signifies a radical of formula (a), R 4 11 signifies an unsubstituted or substituted alkyl or phenyl radical or a radical, (ii) where A signifies a radical of formula (b), R 4 11 signifies an alkoxy or phenoxy radical, (iii) where A signifies a radical of formula (c), R 4 11 signifies an unsubstituted or substituted phenyl radical, and (iv) when A signifies a radical of formula (d), R 4 11 has a significance other than an unsubstituted or substituted phenyl radical, are prepared by a novel method for the production of compounds of the formula in which R 3 is an optionally substituted striazinyl or pyrimidul radical and R 4 is a phenoxy radical or an optionally substituted alkyl, alkoxy, phenyl or amino radical, either by (a) hydrolytically splitting off an acyl radical of the formula R 4 CO- or R 4 1CO- from a compound of the formula wherein R 4 1 has one of the significancies of R 4 , or (b) reacting a compound of the formula with a compound of the formula R 3 .Hal wherein Hal is chlorine or bromine, in a strongly alkaline medium. The novel compounds are useful as intermediates in the preparation of dyestuffs as described in Specification 1,451,493.
149 FR2192147B3 - FR7325421 1973-07-11 FR2192147B3 1976-06-25
150 NL7409231A - NL7409231 1974-07-08 NL7409231A 1974-11-25
151 FR2192147A1 - FR7325421 1973-07-11 FR2192147A1 1974-02-08
152 A process for dyeing wool and silk DEH0113724 1927-11-04 DE490768C 1930-02-06
153 Procedimiento para la estimación de la concentración de fosfatos en células vivas, colorante xanténico y síntesis del mismo ES201330861 2013-06-10 ES2474916B1 2015-04-21 ALVAREZ PEZ JOSÉ MARÍA; CROVETTO GONZALEZ LUIS; CUERVA CARVAJAL JUAN MANUEL; GIRON GONZALEZ MARÍA DOLORES; JUSTICIA LADRON DE GUEVARA JOSÉ; ORTE GUTIERREZ ANGEL; RUEDAS RAMA MARÍA JOSÉ; SALTO GONZALEZ RAFAEL; TALAVERA RODRIGUEZ EVA MARÍA; MARTINEZ PERAGON ANGELA; PAREDES MARTINEZ JOSÉ MANUEL
Procedimiento para la estimación de la concentración de fosfatos en células vivas, colorante xanténico y síntesis del mismo.#La presente invención describe un procedimiento de estimación de la concentración de fosfatos presente en células vivas a través de la medición del tiempo de decaimiento de fluorescencia de un colorante xanténico añadido a las células y sometido a una excitación mediante luz láser pulsada. También se describe un nuevo colorante xanténico derivado de la fluoresceína que posee mejores propiedades espectrales que los ya conocidos y un procedimiento de síntesis de dicho colorante.
154 METODO PARA INHIBIR LA FORMACION Y DEPOSITO DE SARRO EN UN PROCESO DE DESALINIZACION QUE COMPRENDE AGREGAR A UNA FUENTE ACUOSA SALINA UNA CANTIDAD EFECTIVA DE UNA COMPOSICION QUE INHIBE EL SARRO INCLUYENDO UN ACIDO FOSFINICO SUCCINICO OLIGOMERICO. CL2008000082 2008-01-11 CL2008000082A1 2008-07-04 DAVE BHASKER B; RAO NARASIMHA M; YANG SHUNONG; GRATTAN DAVID A; BLOKKER PETER
155 A process for preparing benzoquinones by oxidation of phenols DE59403866 1994-12-13 DE59403866D1 1997-10-02 GESSNER THOMAS DR
156 WATER-COMPATIBLE REDUCIBLE COMPOUNDS AND THEIR USE IN ANALYTICAL COMPOSITIONS AND METHODS CA515164 1986-08-01 CA1281715C 1991-03-19 MURA ALBERT J; BELLY ROBERT T; LUM VANESSA R
WATER-COMPATIBLE REDUCIBLE COMPOUNDS AND THEIR USE IN ANALYTICAL COMPOSITIONS AND METHODS Certain water-compatible reducible compounds are useful in analytical compositions and elements for assay of various analytes, e.g. microorganisms. These compounds comprise a moiety which provides a detectable species (e.g. a dye) when released from the compound at physiological pH. Further, these compounds are aromatic derivatives or quinones having water-compatibilizing substituents which allow them to be used in compositions without the use of surfactants.
157 A PROCESS FOR DYEING HAIR GB8716945 1987-07-17 GB2192645B 1990-04-25 GROLLIER JEAN-FRANCOIS
158 Hair Dyeing Method with hydroxyquinoniques dyes and metal salts LU86521 1986-07-18 LU86521A1 1988-02-02 GROLLIER JEAN-FRANCOIS
159 A method for dyeing hair with hydroxychinonfarbstoffen and metal salts DE3723749 1987-07-17 DE3723749A1 1988-01-21 GROLLIER JEAN-FRANCOIS
160 LIQUID CRYSTAL DIELECTRIC, NEW DYESTUFFS, PROCESS FOR THEIR PREPARATION, AND ELECTRO-OPTIC DISPLAY ELEMENT SG64386 1986-07-24 SG64386G 1987-09-18
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