AR050754A1 - Composicion para el tenido de las fibras queratinicas, y procedimientos y dispositivo de tenido que la utilizan - Google Patents
Composicion para el tenido de las fibras queratinicas, y procedimientos y dispositivo de tenido que la utilizanInfo
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- AR050754A1 AR050754A1 ARP990104096A ARP990104096A AR050754A1 AR 050754 A1 AR050754 A1 AR 050754A1 AR P990104096 A ARP990104096 A AR P990104096A AR P990104096 A ARP990104096 A AR P990104096A AR 050754 A1 AR050754 A1 AR 050754A1
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- Prior art keywords
- radical
- alkyl
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- hydrogen atom
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- 102000011782 Keratins Human genes 0.000 title abstract 5
- 108010076876 Keratins Proteins 0.000 title abstract 5
- 239000000835 fiber Substances 0.000 title abstract 5
- 238000000034 method Methods 0.000 title abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 18
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 12
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 8
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 8
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 8
- 229910052794 bromium Inorganic materials 0.000 abstract 8
- 229910052801 chlorine Inorganic materials 0.000 abstract 8
- 239000000460 chlorine Substances 0.000 abstract 8
- 229910052731 fluorine Inorganic materials 0.000 abstract 8
- 239000011737 fluorine Substances 0.000 abstract 8
- 125000005843 halogen group Chemical group 0.000 abstract 8
- 239000011630 iodine Substances 0.000 abstract 8
- 229910052740 iodine Inorganic materials 0.000 abstract 8
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 7
- 150000001450 anions Chemical class 0.000 abstract 7
- 150000001875 compounds Chemical class 0.000 abstract 6
- 229910052757 nitrogen Inorganic materials 0.000 abstract 6
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 abstract 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- 150000003242 quaternary ammonium salts Chemical class 0.000 abstract 4
- 229910052717 sulfur Inorganic materials 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 229910019142 PO4 Inorganic materials 0.000 abstract 3
- 150000001242 acetic acid derivatives Chemical class 0.000 abstract 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 3
- 150000004820 halides Chemical class 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 239000001301 oxygen Substances 0.000 abstract 3
- 235000021317 phosphate Nutrition 0.000 abstract 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000008051 alkyl sulfates Chemical class 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 2
- 150000003893 lactate salts Chemical class 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 abstract 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- HSMPSHPWCOOUJH-UHFFFAOYSA-N anilinyl Chemical compound [NH]C1=CC=CC=C1 HSMPSHPWCOOUJH-UHFFFAOYSA-N 0.000 abstract 1
- 125000002091 cationic group Chemical group 0.000 abstract 1
- JEVCWSUVFOYBFI-UHFFFAOYSA-N cyanyl Chemical compound N#[C] JEVCWSUVFOYBFI-UHFFFAOYSA-N 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- 239000000982 direct dye Substances 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 238000004043 dyeing Methods 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 abstract 1
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 abstract 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 abstract 1
- 239000003760 tallow Substances 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/416—Quaternary ammonium compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4913—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid
- A61K8/492—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid having condensed rings, e.g. indol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4926—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4946—Imidazoles or their condensed derivatives, e.g. benzimidazoles
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4953—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom containing pyrimidine ring derivatives, e.g. minoxidil
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Coloring (AREA)
Abstract
Una composicion de tenido para fibras queratínicas, en particular para fibras queratínicas humanas tales como los cabellos, que comprende, en un medio adecuado para el tenido, al menos un colorante directo cationico de formula dada, y que se caracteriza por el hecho de que contiene además al menos una sal de amonio cuaternario. El colorante directo es un compuesto seleccionado entre los de formulas (1) a (5), en los cuales los sustituyentes en las formulas (1) a (5) son como se definen en la descripcion; la sal de amonio cuaternario se selecciona entre el grupo que comprende: ii)1 las de formula (6), en la cual, los radicales R1 a R4, idénticos o diferentes, designan un radical hidrocarbonado alifático saturado o insaturado, lineal o ramificado, que comprende de 1 a aproximadamente 30 átomos de carbono, o un radical alcoxi, alcoxicarbonilo, polioxialquileno, alquilamido, alquilamidoalquilo, hidroxialquilo, aromático, arilo, alquilarilo, que comprenden aproximadamente de 12 a aproximadamente 30 átomos de carbono, con al menos un radical entre R1, R2, R3, R4 que designan un radical que comprende de C8-30; X- es un anion seleccionado entre el grupo de los halogenuros, fosfatos, acetatos, lactatos, alquilsulfatos; ii)2 las sales del imidazolio de formula (7), en la cual, R5 es elegido entre los radicales alquenilo y/o alquilos que comprende C13-31 y derivados de los ácidos grasos del sebo; ii)3 las sales de amonio cuaternario de formula (8), en la cual, R6 designa un radical alifático que comprende aproximadamente 16 a 30 átomos de carbono, R7, R8, R9, R10, y R11 son elegidos entre el hidrogeno o un radical alquilo C1-4; y X- es un anion seleccionado entre el grupo de los halogenuros, acetatos, fosfatos y sulfatos. Procedimientos y dispositivos de tenido que la utilizan. Reivindicacion 1: Composicion para el tenido de las fibras queratínicas y en particular de las fibras queratínicas humanas tales como los cabellos, que incluye en un medio adecuado para el tinte, i) al menos un compuesto seleccionado entre los de formulas (1) a (5), en donde: a) los compuestos de formula (1), en la cual, D representa un átomo de nitrogeno o el grupo -CH, R1 y R2, idénticos o diferentes, representan un átomo de hidrogeno; un radical alquilo C1-4 que puede ser sustituido por un radical -CN, -OH o -NH o forman con un átomo de carbono del ciclo bencénico un heterociclo eventualmente oxigenado o nitrogenado, que puede ser sustituido por uno o varios radicales alquilo C1-4; un radical 4-aminofenilo, R3 y R3', idénticos o diferentes, representan un átomo de hidrogeno o de halogeno seleccionado entre el cloro, el bromo, el yodo y el fluor, un radical ciano, alquilo C1-4, alcoxi C1-4 o acetiloxi; X- representa un anion de preferencia elegido entre el cloruro, el metil sulfato o el acetato; A representa un grupo seleccionado por las estructuras de formulas (9) a (27), en las cuales R4 representa un radical alquilo C14 que puede ser sustituido por un radical hidroxilo y R5 representa un radical alcoxi C1-4, con la condicion de que cuando D representa -CH, A representa A4, o A13 y R3 es diferente de un radical alcoxi, entonces R1 y R2 no designan simultáneamente un átomo de hidrogeno; b) los compuestos de formula (2), en la cual: R6 representa un átomo de hidrogeno o un radical alquilo C1-4; R7 representa un átomo de hidrogeno, un radical alquilo que puede ser sustituido por un radical -CN o por un grupo amino, un radical 4'- aminofenilo o forma con R6 un heterociclo eventualmente oxigenado y/o nitrogenado que puede ser sustituido por un radical alquilo C1-4; R8 y R9, idénticos o diferentes, representan un átomo de hidrogeno, un átomo de halogeno tal como el bromo, el cloro, el yodo o el fluor, un radical alquilo C1-4 o alcoxi C1-4, un radical -CN; X- representa un anion de preferencia elegido entre el cloruro, el metil sulfato y el acetato; B representa un grupo seleccionado por las estructuras de formulas (28) a (33), en las cuales R10 representa un radical alquilo C1-4, R11 y R12, idénticos o diferentes, representan un átomo de hidrogeno o un radical alquilo C1-4; c) los compuestos de formulas (3) y (4), en las cuales, R13 representa un átomo de hidrogeno, un radical alcoxi C1-4, un átomo de halogeno tal como el bromo, el cloro, el yodo o el fluor o un radical amino; R14 representa un átomo de hidrogeno, un radical alquilo de C1-4 o forma con un átomo de carbono del ciclo bencénico un heterociclo eventualmente oxigenado y/o sustituido por uno o varios grupos alquilo C1-4; R15 representa un átomo de hidrogeno o de halogeno tal como el bromo, el cloro, el yodo o el fluor; R16 y R17, idénticos o diferentes, representan un átomo de hidrogeno o un radical alquilo C1-4; D1 y D2, idénticos o diferentes, representan un átomo de nitrogeno o el grupo -CH; m = 0 o 1; entendiéndose que cuando R13 representa un grupo amino no sustituido, entonces D1 y D2 representan simultáneamente un grupo -CH y m = 0; X- representa un anion de preferencia elegido entre el cloruro, el metil sulfato o el acetato; E representa un grupo seleccionado por las estructuras de formulas (34) a (41), en las cuales R' representa un radical alquilo C1-4; cuando m = y D1 representa un átomo de nitrogeno, entonces E puede igualmente designar un grupo de estructura de formula (42), en la cual R' representa un radical alquilo C1-4; d) los compuestos de formula (5), en la cual: el símbolo G representa un grupo elegido entre las estructuras de formulas (43) a (45), en las cuales, R18 designan radical alquilo C1-4, un radical fenilo que puede ser sustituido por un radical alquilo C1-4 o un átomo de halogeno seleccionado entre el cloro, el bromo, el yodo y el fluor; R19 designa un radical alquilo C1-4 o un radical fenilo; R20 y R21 idénticos o diferentes, representan un radical alquilo C1-4, un radical fenilo, o forman juntos en la formula (43) un ciclo bencénico sustituido por uno o varios radicales alquilo C1-4, alcoxi C1-4, o NO2, o forman juntos en la formula (44) un ciclo bencénico eventualmente sustituido por uno o varios radicales alquilo C1-4, alcoxi C1-4, o NO2; R20 puede designar además un átomo de hidrogeno; Z designa un átomo de oxígeno, de azufre o un grupo -NR19; M representa un grupo -CH, -CR (designado R alquilo C1-4), -NR22(X-)r; K representa un grupo -CH, -CR (designando R alquilo C1-4), o -NR22(X-)r; P representa un grupo -CH, -CR (designando R alquilo C1- 4), o -NR22(X-)r, donde r designa cero o 1; R22 representa un átomo O-, un radical alcoxi C1-4, o un radical alquilo C1-4; R23 y R24, idénticos o diferentes, representan un átomo de hidrogeno o de halogeno seleccionado entre el cloro, el bromo, el yodo y el fluor, un radical alquilo C1-4, alcoxi C1-4, un radical -NO2; X- representa un anion de preferencia elegido entre el cloruro, el yoduro, el metil sulfato, el etil sulfato, el acetato y el perclorato; con la condicion de que, si R22 designa O-, entonces r designa cero; si K o P o M designan -N-alquiloC1-4X-, entonces R23 o R24 es diferente de un átomo de hidrogeno; si K designa -NR22(X-)r, entonces M = P = -CH, -CR; si M designa -NR2(X-)r, entonces K = P = -CH, -CR; si P designa - NR22(X-)r, entonces K = M y designan -CH o -CR; si Z designa un átomo de azufre con R21 que designa alquilo C1-4, entonces R20 es diferente de un átomo de hidrogeno; si Z designa -NR22 con R19 que designa alquilo C1-4, entonces al menos uno de los radicales R18, R20 o R21 de formula (44) es diferente de un radical alquilo C1-4; el símbolo J representa: a) un grupo de estructura de formula (45), en la cual, R25 representa un átomo de hidrogeno, un átomo de halogeno seleccionado entre el cloro, el bromo, el yodo y el fluor, un radical alquilo C1-4, alcoxi C1-4, un radical -OH, -NO2, -NHR28, -NR29R30, -NHCOalquiloC1-4, o forma con R26 un ciclo de 5 o 6 eslabones conteniendo o no uno o varios heteroátomos seleccionados entre el nitrogeno, el oxígeno o el azufre; R26 representa un átomo de hidrogeno, un átomo de halogeno seleccionado entre el cloro, el bromo, el yodo y el fluor, un radical alquilo C1-4, alcoxi C1-4, o forma con R27 o R28 un ciclo de 5 o 6 eslabones conteniendo o no uno o varios heteroátomos seleccionados entre el nitrogeno, el oxígeno o el azufre; R27 representa un átomo de hidrogeno, un radical -OH, un radical -NHR28, un radical -NR29R30; R28 representa un átomo de hidrogeno, un radical alquilo C1-4, un radical monohidroxialquilo C1-4, polihidroxialquilo C2-4, un radical fenilo; R29 y R30, idénticos o diferentes, representan un radical alquilo C1-4, un radical monohidroxialquilo C1-4, polihidroxialquilo C2-4; b) un grupo heterocíclico nitrogenado de 5 o 6 eslabones susceptibles de incluir otros heteroátomos y/o grupos carbonilados y pudiendo ser sustituido por uno o varios radicales alquilo C1-4, amino o fenilo, y particularmente un grupo de estructura de formulas (46), en la cual, R31 y R32, idénticos o diferentes, representan un átomo de hidrogeno, un radical alquilo C1-4, un radical fenilo; Y designa el radical -CO- o el radical -C(CH3)=; n = 0 o 1, con, cuando n designa 1, U designa el radical -CO-; caracterizándose la indicada composicion por el hecho de que la misma contiene además ii) al menos una sal de amonio cuaternario seleccionado entre el grupo que comprende: ii)1 las de formulas (6), en la cual, los radicales R1 a R4, idénticos o diferentes, designan un radical hidrocarbonado alifático saturado o insaturado, lineal o ramificado, que comprende de 1 a aproximadamente 30 átomos de carbono, o un radical alcoxi, alcoxicarbonilalquilo, polioxialquileno, alquilamido, alquilamidoalquilo, hidroxialquilo, aromático, arilo, alquilarilo, que comprenden aproximadamente de 12 a aproxidamente 30 átomos de carbono, con al menos un radical entre R1, R2, R3, R4 que designan un radical que comprende C8-30; X- es un anion seleccionado entre el grupo de los halogenuros, fosfatos, acetatos, lactatos, alquilsulfatos; ii2) las sales del imidazolilo de formula (7), en la cual, R5 es el
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9810547A FR2782451B1 (fr) | 1998-08-19 | 1998-08-19 | Composition de teinture pour fibres keratiniques avec un colorant direct cationique et un sel d'ammonium quaternaire |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR050754A1 true AR050754A1 (es) | 2006-11-22 |
Family
ID=9529775
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP990104096A AR050754A1 (es) | 1998-08-19 | 1999-08-17 | Composicion para el tenido de las fibras queratinicas, y procedimientos y dispositivo de tenido que la utilizan |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US7087096B2 (es) |
| EP (1) | EP1047387B1 (es) |
| JP (2) | JP2002523344A (es) |
| KR (1) | KR100391696B1 (es) |
| CN (1) | CN100346769C (es) |
| AR (1) | AR050754A1 (es) |
| AT (1) | ATE275384T1 (es) |
| AU (1) | AU729082B2 (es) |
| BR (1) | BR9906730A (es) |
| CA (1) | CA2305504C (es) |
| CZ (1) | CZ20001691A3 (es) |
| DE (1) | DE69919980T2 (es) |
| ES (1) | ES2229739T3 (es) |
| FR (1) | FR2782451B1 (es) |
| HU (1) | HUP0004830A2 (es) |
| MX (1) | MX227264B (es) |
| PL (1) | PL198650B1 (es) |
| PT (1) | PT1047387E (es) |
| RU (1) | RU2197949C2 (es) |
| WO (1) | WO2000010517A1 (es) |
| ZA (1) | ZA200001562B (es) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2817466B1 (fr) | 2000-12-04 | 2004-12-24 | Oreal | Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere associatif et un agent nacrant |
| FR2817467B1 (fr) | 2000-12-04 | 2003-01-10 | Oreal | Composition de teinture pour fibres keratiniques comprenant un polymere associatif et un polymere a motifs acrylamide, halogenure de dialkyldiallylammonium et acide carboxylique vinylique |
| FR2833837B1 (fr) | 2001-12-21 | 2005-08-05 | Oreal | Composition pour la teinture d'oxydation des fibres keratiniques comprenant un amide d'acide gras de colza oxyethylene |
| WO2004020530A1 (en) | 2002-08-30 | 2004-03-11 | Ciba Specialty Chemicals Holding Inc. | Coloured gloss pigments having at least one coating of siox, with x=0.03 to 0.95 for use in cosmetic and personal care formulations |
| FR2887769B1 (fr) * | 2005-06-30 | 2010-12-17 | Oreal | Utilisation de colorants azoiques comprenant une fonction sulfonamide ou amide pour la coloration de fibres keratiniques humaines et procede de coloration et composition tinctoriale les comprenant |
| US7497878B2 (en) | 2005-06-30 | 2009-03-03 | L'oreal, S.A. | Azo dyes containing a sulphonamide or amide function for the dyeing of human keratin fibers and method of dyeing and dyeing compositions containing them |
| EP2029674B1 (en) | 2006-06-13 | 2013-05-22 | Basf Se | Tricationic dyes |
| WO2008049768A1 (en) * | 2006-10-25 | 2008-05-02 | L'oreal | Composition for the direct dyeing of keratinous fibres comprising at least one ammonium salt of 18mea and at least one direct dye, colouring method starting from the composition |
| FR2907670B1 (fr) * | 2006-10-25 | 2008-12-26 | Oreal | Composition pour la teinture directe des fibres keratiniques comprenant au moins un sel d'ammonium du 18mea et au moins un colorant direct cationique, procede de coloration a partir de la composition. |
| EP2076237A1 (en) * | 2006-10-25 | 2009-07-08 | L'Oreal | Composition for oxidation dyeing keratinous fibres comprising at least one particular ammonium salt derived from 18mea, and a colouring method using the composition |
| FR2907671B1 (fr) * | 2006-10-25 | 2008-12-26 | Oreal | Composition pour la teinture des fibres keratiniques comprenant au moins un sel d'ammonium particulier derive du 18mea, au moins du ceramide et procede de coloration a partir de la composition. |
| FR2910282B1 (fr) * | 2006-12-21 | 2009-06-05 | Oreal | Composition de teinture directe comprenant un tensio-actif cationique, un bioheteropolysaccharide, un tensio-actif amphotere ou non ionique et un colorant direct |
| EP2331669B1 (en) * | 2008-09-23 | 2013-12-04 | Unilever Plc, A Company Registered In England And Wales under company no. 41424 of Unilever House | Cationic pyridine and pyridazine dyes |
| EP2400947A2 (en) * | 2009-02-25 | 2012-01-04 | Basf Se | Hair dyeing composition |
| FR2967896B1 (fr) * | 2010-11-25 | 2013-07-05 | Oreal | Composition pour colorer ou decolorer les fibres keratiniques comprenant un tensioactif cationique renfermant une chaine grasse |
| US9565915B2 (en) | 2011-11-09 | 2017-02-14 | L'oreal | Compositions and methods for altering the appearance of hair |
| CN104039296A (zh) | 2011-11-09 | 2014-09-10 | 欧莱雅 | 一种改变头发外观的组合物及方法 |
| BR112015010447B1 (pt) | 2012-11-09 | 2019-12-03 | Oreal | método de alteração da aparência do cabelo |
| EP2916916B1 (en) | 2012-11-09 | 2018-01-10 | L'Oréal | Methods for altering the color and appearance of hair |
| WO2015059368A1 (fr) | 2013-09-02 | 2015-04-30 | L'oreal | Procede de coloration des fibres keratiniques a partir de colorants cationiques styryles disulfures, et composition comprenant lesdits colorants |
| US9018150B1 (en) | 2013-12-09 | 2015-04-28 | L'oreal | Cleansing composition with cationic surfactants |
| US9066859B1 (en) | 2013-12-09 | 2015-06-30 | L'oreal | Viscoelastic cleansing gel |
| BR112016030656B1 (pt) | 2014-10-31 | 2021-01-12 | L'oreal | composições cosméticas, composição aquosa e processo de tratamento cosmético |
| WO2016094973A1 (en) | 2014-12-16 | 2016-06-23 | L'oreal | Cosmetic conditioning composition including a fixative |
| EP3271423B1 (en) * | 2015-03-19 | 2022-08-31 | Basf Se | Cationic direct dyes |
| WO2016149430A1 (en) * | 2015-03-19 | 2016-09-22 | The Procter & Gamble Company | Compositions for dyeing hair with cationic direct dyes |
| US10034823B2 (en) | 2016-09-16 | 2018-07-31 | Noxell Corporation | Method of coloring hair with washfast blue imidazolium direct dye compounds |
| EP3512488B1 (en) * | 2016-09-13 | 2023-12-06 | Wella Operations US, LLC | Hair color compositions comprising stable violet-blue to blue imidazolium dyes |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1373081A (en) * | 1970-11-06 | 1974-11-06 | Unilever Ltd | Colourant compositions for keratinous fibres |
| LU70835A1 (es) * | 1974-08-30 | 1976-08-19 | ||
| FR2140205B1 (es) * | 1971-06-04 | 1977-12-23 | Oreal | |
| US3985499A (en) | 1971-06-04 | 1976-10-12 | L'oreal | Diazamerocyanines for dyeing keratinous fibers |
| LU65539A1 (es) * | 1972-06-19 | 1973-12-21 | ||
| LU71015A1 (es) * | 1974-09-27 | 1976-08-19 | ||
| FR2586913B1 (fr) * | 1985-09-10 | 1990-08-03 | Oreal | Procede pour former in situ une composition constituee de deux parties conditionnees separement et ensemble distributeur pour la mise en oeuvre de ce procede |
| GB8724254D0 (en) * | 1987-10-15 | 1987-11-18 | Unilever Plc | Hair treatment product |
| DE3917304A1 (de) * | 1989-05-27 | 1990-11-29 | Wella Ag | Oxidationshaarfaerbemittel |
| DE4129926C1 (es) * | 1991-09-09 | 1992-07-23 | Kao Corporation Gmbh, 4000 Duesseldorf, De | |
| TW311089B (es) * | 1993-07-05 | 1997-07-21 | Ciba Sc Holding Ag | |
| US5376146A (en) * | 1993-08-26 | 1994-12-27 | Bristol-Myers Squibb Company | Two-part aqueous composition for coloring hair, which forms a gel on mixing of the two parts |
| TW325998B (en) * | 1993-11-30 | 1998-02-01 | Ciba Sc Holding Ag | Dyeing keratin-containing fibers |
| FR2724560B1 (fr) * | 1994-09-21 | 1996-12-20 | Oreal | Procede de coloration directe des fibres keratiniques a l'aide de colorants directs cationiques et de vapeur d'eau |
| WO1997019998A1 (en) * | 1995-11-30 | 1997-06-05 | Novo Nordisk A/S | An enzyme for dying keratinous fibres |
| EP0819422B1 (en) * | 1996-07-15 | 1999-10-27 | Kao Corporation | Composition for dyeing of human hair |
| FR2755854B1 (fr) * | 1996-11-15 | 1998-12-24 | Oreal | Nanoemulsion a base de lipides amphiphiles non-ioniques et cationiques et utilisations |
| FR2757388B1 (fr) * | 1996-12-23 | 1999-11-12 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| FR2757384B1 (fr) | 1996-12-23 | 1999-01-15 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| KR100336678B1 (ko) * | 1997-10-22 | 2002-05-13 | 조지안느 플로 | 케라틴 섬유용 염료 조성물 및 이를 사용한 염색 방법 |
| NZ336320A (en) * | 1997-10-22 | 2001-02-23 | Oreal | Composition for dyeing keratin fibres and dyeing method using same |
-
1998
- 1998-08-19 FR FR9810547A patent/FR2782451B1/fr not_active Expired - Lifetime
-
1999
- 1999-07-28 PL PL340005A patent/PL198650B1/pl unknown
- 1999-07-28 PT PT99934800T patent/PT1047387E/pt unknown
- 1999-07-28 AU AU50454/99A patent/AU729082B2/en not_active Ceased
- 1999-07-28 AT AT99934800T patent/ATE275384T1/de not_active IP Right Cessation
- 1999-07-28 DE DE69919980T patent/DE69919980T2/de not_active Expired - Lifetime
- 1999-07-28 JP JP2000565840A patent/JP2002523344A/ja not_active Withdrawn
- 1999-07-28 RU RU2000112412/14A patent/RU2197949C2/ru not_active IP Right Cessation
- 1999-07-28 KR KR20007004140A patent/KR100391696B1/ko not_active Expired - Fee Related
- 1999-07-28 ES ES99934800T patent/ES2229739T3/es not_active Expired - Lifetime
- 1999-07-28 CA CA002305504A patent/CA2305504C/fr not_active Expired - Fee Related
- 1999-07-28 HU HU0004830A patent/HUP0004830A2/hu unknown
- 1999-07-28 CN CNB998018716A patent/CN100346769C/zh not_active Expired - Fee Related
- 1999-07-28 CZ CZ20001691A patent/CZ20001691A3/cs unknown
- 1999-07-28 WO PCT/FR1999/001865 patent/WO2000010517A1/fr not_active Ceased
- 1999-07-28 EP EP99934800A patent/EP1047387B1/fr not_active Revoked
- 1999-07-28 BR BR9906730-7A patent/BR9906730A/pt not_active IP Right Cessation
- 1999-08-17 AR ARP990104096A patent/AR050754A1/es unknown
-
2000
- 2000-03-28 ZA ZA200001562A patent/ZA200001562B/xx unknown
- 2000-04-10 MX MXPA00003502 patent/MX227264B/es not_active IP Right Cessation
-
2004
- 2004-07-01 US US10/880,615 patent/US7087096B2/en not_active Expired - Lifetime
-
2006
- 2006-03-21 US US11/384,520 patent/US7198652B2/en not_active Expired - Lifetime
-
2007
- 2007-09-20 JP JP2007244536A patent/JP2008044959A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| US7198652B2 (en) | 2007-04-03 |
| JP2002523344A (ja) | 2002-07-30 |
| FR2782451A1 (fr) | 2000-02-25 |
| US20050071933A1 (en) | 2005-04-07 |
| ZA200001562B (en) | 2000-10-24 |
| PL340005A1 (en) | 2001-01-15 |
| US7087096B2 (en) | 2006-08-08 |
| US20060156487A1 (en) | 2006-07-20 |
| AU5045499A (en) | 2000-03-14 |
| HUP0004830A2 (hu) | 2001-05-28 |
| AU729082B2 (en) | 2001-01-25 |
| CN1287482A (zh) | 2001-03-14 |
| WO2000010517A1 (fr) | 2000-03-02 |
| CN100346769C (zh) | 2007-11-07 |
| RU2197949C2 (ru) | 2003-02-10 |
| BR9906730A (pt) | 2000-08-22 |
| PT1047387E (pt) | 2005-01-31 |
| KR20010031197A (ko) | 2001-04-16 |
| MXPA00003502A (es) | 2000-11-01 |
| FR2782451B1 (fr) | 2004-04-09 |
| CA2305504C (fr) | 2008-10-21 |
| DE69919980D1 (de) | 2004-10-14 |
| DE69919980T2 (de) | 2005-09-15 |
| MX227264B (en) | 2005-04-15 |
| KR100391696B1 (ko) | 2003-07-12 |
| EP1047387B1 (fr) | 2004-09-08 |
| CZ20001691A3 (cs) | 2000-08-16 |
| ATE275384T1 (de) | 2004-09-15 |
| JP2008044959A (ja) | 2008-02-28 |
| CA2305504A1 (fr) | 2000-03-02 |
| EP1047387A1 (fr) | 2000-11-02 |
| ES2229739T3 (es) | 2005-04-16 |
| PL198650B1 (pl) | 2008-07-31 |
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| FB | Suspension of granting procedure |