BR112018010344B1 - Composição para cabelo, sistema e método para tratamento do cabelo, métodos para alteração da cor do cabelo e do formato do cabelo, e, kits de multicompartimentos - Google Patents
Composição para cabelo, sistema e método para tratamento do cabelo, métodos para alteração da cor do cabelo e do formato do cabelo, e, kits de multicompartimentos Download PDFInfo
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- BR112018010344B1 BR112018010344B1 BR112018010344-6A BR112018010344A BR112018010344B1 BR 112018010344 B1 BR112018010344 B1 BR 112018010344B1 BR 112018010344 A BR112018010344 A BR 112018010344A BR 112018010344 B1 BR112018010344 B1 BR 112018010344B1
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Images
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
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| CN108495686A (zh) | 2015-11-24 | 2018-09-04 | 欧莱雅 | 用于处理毛发的组合物 |
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| US11135150B2 (en) | 2016-11-21 | 2021-10-05 | L'oreal | Compositions and methods for improving the quality of chemically treated hair |
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| JP7508189B2 (ja) * | 2017-07-27 | 2024-07-01 | 株式会社 資生堂 | 毛髪強化剤 |
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| JP7402603B2 (ja) * | 2018-07-13 | 2023-12-21 | 株式会社ミルボン | 前処理剤、及び酸化染毛方法又は脱色方法 |
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Family Cites Families (403)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2271378A (en) | 1939-08-30 | 1942-01-27 | Du Pont | Pest control |
| US2273780A (en) | 1939-12-30 | 1942-02-17 | Du Pont | Wax acryalte ester blends |
| US2261002A (en) | 1941-06-17 | 1941-10-28 | Du Pont | Organic nitrogen compounds |
| US2388614A (en) | 1942-05-05 | 1945-11-06 | Du Pont | Disinfectant compositions |
| US2375853A (en) | 1942-10-07 | 1945-05-15 | Du Pont | Diamine derivatives |
| US2454547A (en) | 1946-10-15 | 1948-11-23 | Rohm & Haas | Polymeric quaternary ammonium salts |
| GB713675A (en) | 1951-11-09 | 1954-08-18 | Mozes Juda Lewenstein | Improvements in the preparation of compounds having a narcotic effect and the products obtained thereby |
| GB741307A (en) | 1952-01-03 | 1955-11-30 | Monsavon L Orfal | Hair-treating compositions |
| GB773559A (en) | 1954-01-29 | 1957-04-24 | Gillette Co | Improvements in or relating to meth ods and compositions for permanent waving of hair |
| US2850351A (en) | 1955-08-19 | 1958-09-02 | Joseph E Moore | Process of reacting reduced keratin with cross-linking polyimides or polyamides and chemically modified keratin containing the aforesaid crosslinkages |
| US2961347A (en) | 1957-11-13 | 1960-11-22 | Hercules Powder Co Ltd | Process for preventing shrinkage and felting of wool |
| US3193464A (en) | 1961-05-31 | 1965-07-06 | Sales Affilites Inc | Hydrogen peroxide hair bleaching composition and method |
| US3142623A (en) | 1961-11-15 | 1964-07-28 | Oreal | Permanent waving of hair and analogous processes |
| BE626050A (https=) | 1962-03-30 | |||
| US3227615A (en) | 1962-05-29 | 1966-01-04 | Hercules Powder Co Ltd | Process and composition for the permanent waving of hair |
| US3206462A (en) | 1962-10-31 | 1965-09-14 | Dow Chemical Co | Quaternary poly(oxyalkylene)alkylbis(diethylenetriamine) compounds |
| DE1220969B (de) | 1964-11-25 | 1966-07-14 | Ernst Kruegermeyer & Co Seruba | Verfahren zur Verbesserung strukturgeschaedigter Haare |
| GB1125794A (en) | 1965-01-27 | 1968-08-28 | Iichiro Takeda | Improvements in the straightening of hair |
| DE1492175A1 (de) | 1965-07-07 | 1970-02-12 | Schwarzkopf Gmbh Hans | Verfahren zum Faerben von lebenden Haaren |
| FR1492597A (fr) | 1965-09-14 | 1967-08-18 | Union Carbide Corp | Nouveaux éthers cellulosiques contenant de l'azote quaternaire |
| US3472840A (en) | 1965-09-14 | 1969-10-14 | Union Carbide Corp | Quaternary nitrogen-containing cellulose ethers |
| US3472243A (en) | 1965-09-27 | 1969-10-14 | Clairol Inc | Treating damaged living human hair with water soluble polymerizable vinyl monomers |
| LU49584A1 (https=) | 1965-10-05 | 1967-04-05 | ||
| CH491153A (de) | 1967-09-28 | 1970-05-31 | Sandoz Ag | Verfahren zur Herstellung von neuen kationaktiven, wasserlöslichen Polyamiden |
| US3589978A (en) | 1967-09-29 | 1971-06-29 | Gen Mills Inc | Process of making water repellent paper using a fatty polyisocyanate and a cationic gum ether and product therefrom |
| US3655869A (en) | 1969-01-02 | 1972-04-11 | Monsanto Co | Treatment of diarrhea employing certain basic polyelectrolyte polymers |
| US4013787A (en) | 1971-11-29 | 1977-03-22 | Societe Anonyme Dite: L'oreal | Piperazine based polymer and hair treating composition containing the same |
| FR2280361A2 (fr) | 1974-08-02 | 1976-02-27 | Oreal | Compositions de traitement et de conditionnement de la chevelure |
| LU64371A1 (https=) | 1971-11-29 | 1973-06-21 | ||
| DE2225541A1 (de) | 1972-05-26 | 1973-12-06 | Boris Dr Janistyn | Kosmetische und pharmazeutische zubereitungen |
| DE2359399C3 (de) | 1973-11-29 | 1979-01-25 | Henkel Kgaa, 4000 Duesseldorf | Haarfärbemittel |
| USRE30199E (en) | 1973-11-29 | 1980-01-29 | Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) | Oxidation hair dyes based upon tetraaminopyrimidine developers |
| US4003699A (en) | 1974-11-22 | 1977-01-18 | Henkel & Cie G.M.B.H. | Oxidation hair dyes based upon tetraaminopyrimidine developers |
| US4277581A (en) | 1973-11-30 | 1981-07-07 | L'oreal | Polyamino-polyamide crosslinked with crosslinking agent |
| US4172887A (en) | 1973-11-30 | 1979-10-30 | L'oreal | Hair conditioning compositions containing crosslinked polyaminopolyamides |
| US4189468A (en) | 1973-11-30 | 1980-02-19 | L'oreal | Crosslinked polyamino-polyamide in hair conditioning compositions |
| FR2368508A2 (fr) | 1977-03-02 | 1978-05-19 | Oreal | Composition de conditionnement de la chevelure |
| LU68901A1 (https=) | 1973-11-30 | 1975-08-20 | ||
| US4025627A (en) | 1973-12-18 | 1977-05-24 | Millmaster Onyx Corporation | Microbiocidal polymeric quaternary ammonium compounds |
| US3874870A (en) | 1973-12-18 | 1975-04-01 | Mill Master Onyx Corp | Microbiocidal polymeric quarternary ammonium compounds |
| US3929990A (en) | 1973-12-18 | 1975-12-30 | Millmaster Onyx Corp | Microbiocidal polymeric quaternary ammonium compounds |
| DK659674A (https=) | 1974-01-25 | 1975-09-29 | Calgon Corp | |
| US4166894A (en) | 1974-01-25 | 1979-09-04 | Calgon Corporation | Functional ionene compositions and their use |
| US4422853A (en) | 1974-05-16 | 1983-12-27 | L'oreal | Hair dyeing compositions containing quaternized polymer |
| US4217914A (en) | 1974-05-16 | 1980-08-19 | L'oreal | Quaternized polymer for use as a cosmetic agent in cosmetic compositions for the hair and skin |
| US4948579A (en) | 1974-05-16 | 1990-08-14 | Societe Anonyme Dite: L'oreal | Quaternized polymer for use as a cosmetic agent in cosmetic compositions for the hair and skin |
| CH611156A5 (https=) | 1974-05-16 | 1979-05-31 | Oreal | |
| US5196189A (en) | 1974-05-16 | 1993-03-23 | Societe Anonyme Dite: L'oreal | Quaternized polymer for use as a cosmetic agent in cosmetic compositions for the hair and skin |
| US4005193A (en) | 1974-08-07 | 1977-01-25 | Millmaster Onyx Corporation | Microbiocidal polymeric quaternary ammonium compounds |
| US4025617A (en) | 1974-10-03 | 1977-05-24 | Millmaster Onyx Corporation | Anti-microbial quaternary ammonium co-polymers |
| US4026945A (en) | 1974-10-03 | 1977-05-31 | Millmaster Onyx Corporation | Anti-microbial quaternary ammonium co-polymers |
| US3966904A (en) | 1974-10-03 | 1976-06-29 | Millmaster Onyx Corporation | Quaternary ammonium co-polymers for controlling the proliferation of bacteria |
| US4001432A (en) | 1974-10-29 | 1977-01-04 | Millmaster Onyx Corporation | Method of inhibiting the growth of bacteria by the application thereto of capped polymers |
| US4027020A (en) | 1974-10-29 | 1977-05-31 | Millmaster Onyx Corporation | Randomly terminated capped polymers |
| US4025653A (en) | 1975-04-07 | 1977-05-24 | Millmaster Onyx Corporation | Microbiocidal polymeric quaternary ammonium compounds |
| AT365448B (de) | 1975-07-04 | 1982-01-11 | Oreal | Kosmetische zubereitung |
| US4197865A (en) | 1975-07-04 | 1980-04-15 | L'oreal | Treating hair with quaternized polymers |
| CH1669775A4 (https=) | 1975-12-23 | 1977-06-30 | ||
| US4031307A (en) | 1976-05-03 | 1977-06-21 | Celanese Corporation | Cationic polygalactomannan compositions |
| GB1584364A (en) | 1976-06-21 | 1981-02-11 | Unilever Ltd | Shampoo |
| LU76955A1 (https=) | 1977-03-15 | 1978-10-18 | ||
| LU78153A1 (fr) | 1977-09-20 | 1979-05-25 | Oreal | Compositions cosmetiques a base de polymeres polyammonium quaternaires et procede de preparation |
| US4131576A (en) | 1977-12-15 | 1978-12-26 | National Starch And Chemical Corporation | Process for the preparation of graft copolymers of a water soluble monomer and polysaccharide employing a two-phase reaction system |
| FR2421607A1 (fr) | 1978-04-06 | 1979-11-02 | Oreal | Procede de teinture des fibres keratiniques en deux temps par variation de ph |
| US4348202A (en) | 1978-06-15 | 1982-09-07 | L'oreal | Hair dye or bleach supports |
| US4970066A (en) | 1978-06-15 | 1990-11-13 | L'oreal | Hair dye or bleach supports of quaternized polymers |
| DE2929865A1 (de) | 1979-07-24 | 1981-02-19 | Wella Ag | Verfahren zur dauerhaften haarverformung |
| LU83349A1 (fr) | 1981-05-08 | 1983-03-24 | Oreal | Composition sous forme de mousse aerosol a base de polymere cationique et de polymere anionique |
| US4412934A (en) | 1982-06-30 | 1983-11-01 | The Procter & Gamble Company | Bleaching compositions |
| LU84708A1 (fr) | 1983-03-23 | 1984-11-14 | Oreal | Composition epaissie ou gelifiee de conditionnement des cheveux contenant au moins un polymere cationique,au moins un polymere anionique et au moins une gomme de xanthane |
| DE3375135D1 (en) | 1983-04-15 | 1988-02-11 | Miranol Inc | Polyquaternary ammonium compounds and cosmetic compositions containing them |
| US4770873A (en) | 1983-06-15 | 1988-09-13 | Clairol, Incorporated | Neutralizing composition and method for hair waving and straightening |
| US4812307A (en) | 1983-07-06 | 1989-03-14 | Chesebrough-Pond's Inc. | Crosslinking of hair thiols using glutathione disulfide |
| AU571671B2 (en) | 1984-04-12 | 1988-04-21 | Revlon Inc. | Alkyltrialkosilane hair strengthening and permanent wave composition |
| FR2596985B1 (fr) | 1986-04-10 | 1990-08-24 | Oreal | Compositions cosmetiques pour teindre ou pour decolorer les cheveux |
| DE3627746A1 (de) | 1986-08-16 | 1988-02-18 | Henkel Kgaa | Verfahren zur dauerhaften haarverformung |
| JPH0751492B2 (ja) | 1986-12-17 | 1995-06-05 | 株式会社資生堂 | プレヘアリンス型毛髪処理剤組成物 |
| US5385938B1 (en) | 1986-12-23 | 1997-07-15 | Tristrata Inc | Method of using glycolic acid for treating wrinkles |
| US4793992A (en) | 1987-03-25 | 1988-12-27 | Redken Laboratories, Inc. | Hair treatment composition |
| US4795629A (en) | 1987-07-06 | 1989-01-03 | Chesebrough-Pond's Inc. | Crosslinking of hair thiols using cystamine |
| US4793993A (en) | 1987-07-06 | 1988-12-27 | Chesebrough-Pond's Inc. | Crosslinking of hair thiols |
| ZA885143B (en) | 1987-07-16 | 1990-03-28 | Unilever Plc | Hair treatment product |
| DE3871450D1 (de) | 1987-07-16 | 1992-07-02 | Unilever Nv | Mittel zur haarbehandlung. |
| JP2526099B2 (ja) | 1988-07-07 | 1996-08-21 | 花王株式会社 | 角質繊維染色組成物 |
| US4906460A (en) | 1988-08-05 | 1990-03-06 | Sorenco | Additive for hair treatment compositions |
| DE3843892A1 (de) | 1988-12-24 | 1990-06-28 | Wella Ag | Oxidationshaarfaerbemittel mit einem gehalt an diaminopyrazolderivaten und neue diaminopyrazolderivate |
| FR2654617B1 (fr) | 1989-11-20 | 1993-10-08 | Oreal | Composition cosmetique reductrice pour permanente contenant, en tant qu'agent reducteur, de l'aletheine ou l'un de ses sels, et son utilisation dans un procede de deformation permanente des cheveux. |
| EP0437075B1 (en) | 1990-01-09 | 1993-12-15 | Dow Corning Corporation | Siloxane conditioners for hair |
| FR2676173B1 (fr) | 1991-05-06 | 1993-08-13 | Oreal | Composition cosmetique contenant un agent alcalinisant sans odeur. |
| WO1993000882A1 (en) | 1991-07-08 | 1993-01-21 | R.M. Walker Healthcare Products, Inc. | Neutralizing rinse and improved method for chemically relaxing hair |
| US5293885A (en) | 1991-07-11 | 1994-03-15 | Johnson Products Co., Inc. | Hair relaxer and post-relaxer hair brightener system |
| DE4133957A1 (de) | 1991-10-14 | 1993-04-15 | Wella Ag | Haarfaerbemittel mit einem gehalt an aminopyrazolderivaten sowie neue pyrazolderivate |
| FI941969A0 (fi) | 1991-10-29 | 1994-04-28 | Procter & Gamble | Shampookoostumuksia, jotka sisältävät hoitavina aineina silikonia, kationista polymeeriä ja öljymäistä nestettä |
| JP3053939B2 (ja) | 1991-12-17 | 2000-06-19 | 花王株式会社 | 角質繊維染色組成物 |
| US5221286A (en) | 1992-07-17 | 1993-06-22 | Eastman Kodak Company | Cold mix emulsions used as a developer composition for oxidative hair dyes and for hair bleaches |
| ATE157242T1 (de) | 1992-09-21 | 1997-09-15 | Procter & Gamble | Feuchthaltende lippenstiftzusammensetzungen |
| DE4234887A1 (de) | 1992-10-16 | 1994-04-21 | Wella Ag | Oxidationshaarfärbemittel mit einem Gehalt an 4,5-Diaminopyrazolderivaten sowie neue 4,5-Diaminopyrazolderivate und Verfahren zu ihrer Herstellung |
| DE4234885A1 (de) | 1992-10-16 | 1994-04-21 | Wella Ag | Verfahren zur Herstellung von 4,5-Diaminopyrazol-Derivaten, deren Verwendung zum Färben von Haaren sowie neue Pyrazol-Derivate |
| KR960009640B1 (ko) | 1992-10-16 | 1996-07-23 | 주식회사 태평양 | 헤어칼라린스 조성물 |
| US5663366A (en) | 1992-10-16 | 1997-09-02 | Wella Aktiengesellschat | Process for the synthesis of 4,5-diaminopyrazole derivatives useful for dyeing hair |
| DE4300320A1 (de) | 1993-01-08 | 1994-07-14 | Hartmann Haarkosmetik Gmbh | Mittel und Verfahren zum Zwecke der Herstellung gebrauchsfertiger Dauerwellenpräparate für jede Haarqualität durch mischen von 2 Lösungen, wodurch ein sukzessiver Thio-Gruppen-Verminderungseffekt durch Addition und eine teilweise Neutralisation eintritt |
| US5350572A (en) | 1993-02-18 | 1994-09-27 | Shiseido Co., Ltd. | Permanent waving composition |
| DE4314317A1 (de) | 1993-04-30 | 1994-11-03 | Henkel Kgaa | Isatinhaltige Mittel zum Färben von keratinhaltigen Fasern |
| ES2119213T3 (es) | 1993-06-30 | 1998-10-01 | Procter & Gamble | Champus acondicionadores que contienen cationes metalicos polivalentes. |
| SG72661A1 (en) | 1993-07-01 | 2000-05-23 | Procter & Gamble | Thermoplastic elastomeric copolymers and hair and skin care compositions containing the same |
| TW311089B (https=) | 1993-07-05 | 1997-07-21 | Ciba Sc Holding Ag | |
| US5565216A (en) | 1993-07-21 | 1996-10-15 | Carson Products Company | Hair relaxer compositions |
| FR2708197B1 (fr) | 1993-07-28 | 1995-09-08 | Oreal | Nouvelles compositions à base d'eau oxygénée et leur utilisation comme fixateurs pour permanentes. |
| BR9407627A (pt) | 1993-08-23 | 1997-01-21 | Procter & Gamble | Copolímeros elastoméricos termoplásticos enxertados com silicone e composiçoes para o cuidado da pele e do cabelo contendo os mesmos |
| TW325998B (en) | 1993-11-30 | 1998-02-01 | Ciba Sc Holding Ag | Dyeing keratin-containing fibers |
| JPH08198732A (ja) | 1994-01-27 | 1996-08-06 | Kao Corp | 毛髪処理剤組成物 |
| GB9415911D0 (en) | 1994-08-05 | 1994-09-28 | Unilever Plc | Hair styling composition and method |
| US5635168A (en) | 1994-09-21 | 1997-06-03 | Business Resources Group, Inc. | Composition for treating hair |
| ES2215944T3 (es) | 1994-11-03 | 2004-10-16 | Ciba Specialty Chemicals Holding Inc. | Colorantes imidazolazoicos cationicos. |
| DE4440957A1 (de) | 1994-11-17 | 1996-05-23 | Henkel Kgaa | Oxidationsfärbemittel |
| JP3446365B2 (ja) | 1995-01-27 | 2003-09-16 | 旭硝子株式会社 | インクジェットプリンタ用記録媒体および記録物 |
| FR2733749B1 (fr) | 1995-05-05 | 1997-06-13 | Oreal | Compositions pour la teinture des fibres keratiniques contenant des diamino pyrazoles, procede de teinture, nouveaux diamino pyrazoles et leur procede de preparation |
| US6013250A (en) | 1995-06-28 | 2000-01-11 | L'oreal S. A. | Composition for treating hair against chemical and photo damage |
| US5651960A (en) | 1995-09-22 | 1997-07-29 | Helene Curtis, Inc. | Method and composition for removing semi-permanent color from human hair |
| TW453881B (en) | 1995-10-16 | 2001-09-11 | Kao Corp | Cosmetic composition comprising amide derivatives |
| DE19539264C2 (de) | 1995-10-21 | 1998-04-09 | Goldwell Gmbh | Haarfärbemittel |
| DE19543988A1 (de) | 1995-11-25 | 1997-05-28 | Wella Ag | Oxidationshaarfärbemittel mit einem Gehalt an 3,4,5-Triaminopyrazolderivaten sowie neue 3,4,5-Triaminopyrazolderivate |
| GB9526633D0 (en) | 1995-12-29 | 1996-02-28 | Procter & Gamble | Hair colouring compositions |
| US5688291A (en) | 1996-06-27 | 1997-11-18 | L'avante Garde, Inc. | Composition for simultaneously lightening and coloring hair |
| DE19635877C2 (de) | 1996-09-04 | 2002-10-24 | Goldwell Gmbh | Mittel zur Aufhellung, Glanzverbesserung und Färbung von menschlichen Haaren |
| US6432147B1 (en) | 1996-12-23 | 2002-08-13 | The Procter & Gamble Company | Hair coloring compositions |
| GB9626712D0 (en) | 1996-12-23 | 1997-02-12 | Procter & Gamble | Hair colouring compositions |
| GB9626778D0 (en) | 1996-12-23 | 1997-02-12 | Procter & Gamble | Hair coloring compositions |
| US6309426B1 (en) | 1996-12-23 | 2001-10-30 | The Procter & Gamble Company | Hair coloring compositions |
| US6398821B1 (en) | 1996-12-23 | 2002-06-04 | The Procter & Gamble Company | Hair coloring compositions |
| JP4074352B2 (ja) | 1997-01-27 | 2008-04-09 | 花王株式会社 | 毛髪化粧料 |
| US6015574A (en) | 1997-06-09 | 2000-01-18 | L'oreal | Lipophilic carrier systems |
| EP1011611A1 (en) | 1997-08-29 | 2000-06-28 | The Procter & Gamble Company | Hair conditioning compositions |
| US6241971B1 (en) | 1997-09-25 | 2001-06-05 | The Procter & Gamble Company | Hair styling compositions comprising mineral salt, lipophilic material, and low levels of surfactant |
| US5993792A (en) | 1997-11-13 | 1999-11-30 | Tiro Industries Incorporated | System for customized hair products containing surfactants |
| US5985803A (en) | 1997-12-05 | 1999-11-16 | The Lubrizol Corporation | Polyethoxylated alcohol-based phosphonates for metal working lubricants |
| BR9807422A (pt) | 1997-12-19 | 2000-03-21 | Wella Ag | Processo para dar forma e volume aos cabelos humanos |
| DE29722990U1 (de) | 1997-12-31 | 1999-05-06 | Goldwell GmbH, 64297 Darmstadt | Mittel zum Blondieren und Aufhellen von menschlichen Haaren |
| US6036966A (en) | 1998-02-17 | 2000-03-14 | Youssefyeh; Rena T. | Skin treatment compositions comprising protein and enzyme extracts |
| US20040067212A1 (en) | 1998-03-11 | 2004-04-08 | Kabushiki Kaisha Soken | Skin conditioner |
| GB9808310D0 (en) | 1998-04-20 | 1998-06-17 | Unilever Plc | Shampoo compositions |
| JP2002518414A (ja) | 1998-06-22 | 2002-06-25 | ザ、プロクター、エンド、ギャンブル、カンパニー | 処理を施した拭き取り用品 |
| EP0978272A1 (en) | 1998-08-07 | 2000-02-09 | Kao Corporation | Medulla care preparation |
| JP3208382B2 (ja) | 1998-12-28 | 2001-09-10 | 花王株式会社 | 毛髪洗浄剤 |
| US6299697B1 (en) | 1999-08-25 | 2001-10-09 | Shibaura Mechatronics Corporation | Method and apparatus for processing substrate |
| US6767875B1 (en) | 1999-09-03 | 2004-07-27 | The Procter & Gamble Company | Hair conditioning composition comprising carboxylic acid/carboxylate copolymer and moisturizing agent |
| ATE366129T1 (de) | 1999-11-11 | 2007-07-15 | Procter & Gamble | Haarpflege- und antischuppenmittel |
| FR2801308B1 (fr) | 1999-11-19 | 2003-05-09 | Oreal | COMPOSITIONS DE TEINTURE DE FIBRES KERATINIQUES CONTENANT DE DES 3-AMINO PYRAZOLO-[1,(-a]-PYRIDINES, PROCEDE DE TEINTURE, NOUVELLES 3-AMINO PYRAZOLO-[1,5-a]-PYRIDINES |
| JP3420143B2 (ja) | 1999-12-02 | 2003-06-23 | 花王株式会社 | 毛髪処理剤 |
| FR2802093B1 (fr) | 1999-12-08 | 2002-01-18 | Oreal | Composition pour la decoloration ou la deformation permanente des fibres keratiniques comprenant un polymere epaississant a squelette aminoplaste-ether |
| DE19962869A1 (de) | 1999-12-24 | 2001-06-28 | Henkel Kgaa | Verringerung der Haarschädigung bei oxidativen Prozessen |
| JP3638490B2 (ja) * | 2000-01-07 | 2005-04-13 | 花王株式会社 | 染色毛髪用処理組成物 |
| EP1248966B1 (de) | 2000-01-10 | 2004-01-02 | Siemens Aktiengesellschaft | Universelle bewegungssteuerung |
| JP3696473B2 (ja) | 2000-03-16 | 2005-09-21 | 花王株式会社 | ケラチン質繊維染色剤組成物 |
| US20010042276A1 (en) | 2000-03-30 | 2001-11-22 | Shiseido Co., Ltd. | Hair dye fixatives, hair dyes and hair dyeing methods |
| EP1184364B1 (en) * | 2000-04-07 | 2010-07-28 | Mitsui Chemicals, Inc. | Comb-shaped diol, water-soluble polyurethane, and use thereof |
| CN1297688C (zh) | 2000-05-30 | 2007-01-31 | 杰富意钢铁株式会社 | 具有有机涂层的钢板和其制造方法 |
| CN1186004C (zh) | 2000-06-26 | 2005-01-26 | 株式会社资生堂 | 头发用组合物 |
| TWI278328B (en) | 2000-07-21 | 2007-04-11 | Kao Corp | Hair cosmetic composition |
| FR2813016B1 (fr) | 2000-08-21 | 2002-10-11 | Oreal | Composition de decoloration des fibres keratiniques teintes |
| MXPA03002057A (es) * | 2000-09-08 | 2003-07-24 | Procter & Gamble | Composicion acondicionadora para el cabello que comprende particulas. |
| US20030215415A1 (en) | 2000-09-08 | 2003-11-20 | The Procter & Gamble Company | Hair conditioning compositions comprising particles |
| DE10051773A1 (de) | 2000-10-19 | 2002-04-25 | Henkel Kgaa | Neue Verwendung von kurzkettigen Carbonsäuren |
| DE10051774A1 (de) | 2000-10-19 | 2002-04-25 | Henkel Kgaa | Neue Verwendung von kurzkettigen Carbonsäuren |
| US6426065B1 (en) | 2000-11-07 | 2002-07-30 | Clairol Incorporated | Use of tris(hydroxymethyl)aminomethane in cold permanent waving processes |
| FR2816210B1 (fr) | 2000-11-08 | 2005-02-25 | Oreal | Composition pour la decoloration ou la deformation permanente des fibres keratiniques comprenant un polyurethane associatif cationique |
| FR2818538B1 (fr) | 2000-12-22 | 2003-02-07 | Oreal | Composition pour la teinture d'oxydation des fibres keratiniques comprenant au moins un 4,5 ou 3,4-diamino pyrazole ou un triamino pyrazole et au moins un compose carbonyle selectionne, et procede de teinture |
| FR2819403B1 (fr) | 2001-01-12 | 2004-10-15 | Oreal | Compositions cosmetiques contenant un fructane, un polysaccharide et un agent benefique et leurs utilisations |
| US6602493B2 (en) | 2001-02-15 | 2003-08-05 | Avlon Industries, Inc. | Hair relaxer system and method therefor |
| US7186275B2 (en) | 2001-03-20 | 2007-03-06 | The Procter & Gamble Company | Compositions suitable for the treatment of hair comprising chelants and methods for reducing oxidative hair damage |
| JP2002356408A (ja) | 2001-05-30 | 2002-12-13 | Milbon Co Ltd | ヘアトリートメントおよびそれを用いた毛髪のセット方法 |
| JP2002363048A (ja) | 2001-05-31 | 2002-12-18 | Nicca Chemical Co Ltd | 2剤式染毛・脱色剤組成物用第1剤、2剤式染毛・脱色剤組成物キット、及びそれを用いた毛髪処理方法 |
| US6645478B2 (en) | 2001-06-22 | 2003-11-11 | L'oreal S.A. | Reshapable hair styling composition comprising (meth)acrylic copolymers of four or more monomers |
| KR100761217B1 (ko) | 2001-07-04 | 2007-10-04 | 주식회사 엘지생활건강 | 염모제 조성물 |
| WO2003017959A1 (en) * | 2001-08-30 | 2003-03-06 | Nonogawa Shoji Ltd. | Hair treatment agent composition and method for production thereof |
| FR2831818B1 (fr) | 2001-11-08 | 2004-07-16 | Oreal | Composition oxydante pour le traitement des fibres keratiniques comprenant une silicone aminee particuliere |
| AU2003211241A1 (en) | 2002-02-21 | 2003-09-09 | Yugen Kaisha Okada Giken | Treating agent for protecting animal fiber |
| CN1311003C (zh) | 2002-03-20 | 2007-04-18 | Ge拜尔硅股份有限公司 | 支链聚有机硅氧烷聚合物 |
| DE20208254U1 (de) | 2002-05-28 | 2002-08-29 | Goldwell Gmbh | Haarfärbemittel |
| CA2682799A1 (en) | 2002-06-04 | 2003-12-11 | The Procter & Gamble Company | Conditioning shampoo compositions containing surfactant and cationic copolymer combination that forms liquid crystals |
| KR20050013099A (ko) | 2002-06-25 | 2005-02-02 | 가부시키가이샤 시세이도 | 세정제 조성물 |
| JP4127777B2 (ja) | 2002-08-09 | 2008-07-30 | 花王株式会社 | 毛髪洗浄剤組成物 |
| BRPI0313821B1 (pt) | 2002-08-30 | 2015-04-14 | Isp Investments Inc | Polímeros de toque natural |
| AU2003284595A1 (en) * | 2002-11-26 | 2004-06-18 | Kao Corporation | Cosmetic hair preparation |
| US20040216244A1 (en) | 2002-12-13 | 2004-11-04 | L'oreal | Dyeing composition comprising a cationic tertiary para-phenylenediamine and an organic diacid, methods and uses |
| US20040181883A1 (en) | 2002-12-20 | 2004-09-23 | Frederic Legrand | Pasty anhydrous composition for simultaneously bleaching and dyeing human keratin fibers comprising at least one peroxygenated salt, at least one alkaline agent, at least one inert organic liquid and at least one cationic direct dye; process using such a compound; and kit comprising such a compound |
| CN100438852C (zh) | 2002-12-25 | 2008-12-03 | 花王株式会社 | 毛发清洁剂 |
| US7306662B2 (en) | 2006-05-11 | 2007-12-11 | Lam Research Corporation | Plating solution for electroless deposition of copper |
| US20040202689A1 (en) | 2003-03-17 | 2004-10-14 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Terpenoid fragrance components stabilized with malonic acid salts |
| US20050036970A1 (en) | 2003-03-25 | 2005-02-17 | L'oreal S.A. | Reducing compositions for bleaching or permanently reshaping keratin fibres comprising polycarboxylic acids and salts thereof as complexing agents |
| US7186278B2 (en) | 2003-04-01 | 2007-03-06 | L'oreal S.A. | Composition for dyeing human keratin materials, comprising at least one fluorescent dye and at least one compound comprising an acid functional group and processes therefor |
| KR20040098688A (ko) | 2003-05-15 | 2004-11-26 | 삼성전자주식회사 | 광 모듈 |
| US20040241114A1 (en) | 2003-05-30 | 2004-12-02 | Gupta Shyam K. | Hair Care and Nail Care Compositions Based on Ion-Pair Delivery System for Gender and Ethnic Selective Applications |
| EP1484047A1 (en) * | 2003-06-02 | 2004-12-08 | The Procter & Gamble Company | Hair colouring compositions |
| DE50303835D1 (de) | 2003-06-18 | 2006-07-27 | Goldschmidt Gmbh | Haarbehandlungsmittel und Haarnachbehandlungsmittel zum Schutz vor Schäden durch chemische Behandlung und zur Reparatur bereits geschädigter Haare enthaltend als Wirksubstanz Alkylguanidin-Verbindungen |
| WO2005011623A1 (ja) | 2003-08-01 | 2005-02-10 | Kao Corporation | 毛髪化粧料 |
| JP2005154348A (ja) | 2003-11-26 | 2005-06-16 | Lion Corp | 毛髪化粧料 |
| ATE496615T1 (de) | 2003-12-05 | 2011-02-15 | Kpss Kao Gmbh | Haarkonditionierungs- und reinigungszusammensetzung |
| EP1541117A1 (en) | 2003-12-12 | 2005-06-15 | Tiense Suikerraffinaderij N.V. | Cosmetic rinse-off compositions comprising inulin-type fructan |
| JP4381169B2 (ja) | 2004-02-27 | 2009-12-09 | 花王株式会社 | 毛髪化粧料 |
| JP4422508B2 (ja) | 2004-02-27 | 2010-02-24 | 花王株式会社 | 毛髪化粧料 |
| US7066968B2 (en) | 2004-03-02 | 2006-06-27 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Efficient two-step method of coloring and lightening hair with less damage |
| EP1591102A1 (en) | 2004-04-30 | 2005-11-02 | The Procter & Gamble Company | Process and kit-of-parts for improved hair conditioning after coloring, bleaching or perming |
| KR100684985B1 (ko) | 2004-07-30 | 2007-02-20 | 한국화학연구원 | 자가조형성 퍼머제 |
| WO2006011771A1 (en) | 2004-07-30 | 2006-02-02 | Korea Research Institute Of Chemical Technology | Self-molding permanent agent and method for proceeding free-rod and free-band type permanent |
| LT1791791T (lt) | 2004-09-27 | 2019-09-10 | Special Water Patents B.V. | Vandens valymo būdai ir kompozicijos |
| US7041142B2 (en) | 2004-10-12 | 2006-05-09 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Two step hair coloring compositions delivering deeper, long-lasting color |
| JP2006117606A (ja) | 2004-10-22 | 2006-05-11 | Shiseido Co Ltd | 毛髪化粧料 |
| DE102004052480A1 (de) | 2004-10-28 | 2006-05-04 | Henkel Kgaa | Reduktionsmittel-haltiges Mittel zum Färben von keratinhaltigen Fasern |
| US20060093571A1 (en) | 2004-10-29 | 2006-05-04 | Jan Glinski | Hair and skin protecting compositions based on esters or ethers of betulin |
| KR20060059564A (ko) | 2004-11-29 | 2006-06-02 | 건국대학교 산학협력단 | 약산을 포함하는 모발처리제 |
| FR2880888B1 (fr) | 2005-01-20 | 2010-12-24 | Oreal | Utilisation d'aminodithiol en tant qu'agent reducteur pour la deformation permanente des cheveux |
| US7815901B2 (en) | 2005-01-28 | 2010-10-19 | L'ORéAL S.A. | Hair treatment method |
| US7754194B2 (en) | 2005-04-06 | 2010-07-13 | L'oréal | Hair relaxer compositions utilizing bioactive glass |
| TW200638867A (en) | 2005-05-06 | 2006-11-16 | Golden Biotechnology Corp | Incubation and application methods for the culture of antrodia camphorata |
| JP2006327994A (ja) | 2005-05-26 | 2006-12-07 | Okada Giken:Kk | 毛髪保護剤 |
| FR2886136B1 (fr) | 2005-05-31 | 2007-08-10 | Oreal | Composition pour la teinture des fibres keratiniques comprenant au moins un derive de diamino-n,n-dihydro- pyrazolone et un colorant d'oxydation cationique |
| CN104018364B (zh) | 2005-06-15 | 2017-01-11 | 巴斯夫欧洲公司 | 阳离子低聚偶氮染料 |
| DE102005031705A1 (de) | 2005-07-05 | 2007-01-18 | Henkel Kgaa | Mittel, enthaltend L-Carnitin oder L-Carnitinderivate und mindestens eine weitere Substanz ausgewählt aus Taurin und dessen Derivaten und mindestens einem Wirkstoff, erhältlich aus Pflanzen der Gattung Echinacea |
| ZA200606791B (en) | 2005-08-18 | 2008-05-28 | Unilever Plc | Method for relaxing hair |
| EP1931427A4 (en) | 2005-09-12 | 2008-12-03 | Avlon Ind Inc | KERATIN PROTECTING LOCK MINIMIZING COMPOSITIONS, METHOD AND KIT THEREFOR |
| US7736633B2 (en) | 2005-09-28 | 2010-06-15 | E.I. Du Pont De Nemours And Company | Method for enhancing effects of colorants and conditioners |
| FR2892629B1 (fr) | 2005-10-28 | 2012-04-27 | Oreal | Composition cosmetique comprenant au moins un polymere fixant particulier et au moins un tensioactif ionique et/ou non ionique |
| US20070160560A1 (en) | 2005-10-28 | 2007-07-12 | Ludivine Laurent | Cosmetic composition comprising at least one fixative polymer and at least one surfactant chosen from ionic and nonionic surfactants |
| US7449029B2 (en) | 2005-11-16 | 2008-11-11 | L'oreal | Composition and process for color hair |
| US7820147B2 (en) | 2005-11-18 | 2010-10-26 | Mata Michael T | Hair restorative compositions and methods for treating damaged hair and safely chemically treating hair |
| FR2894816B1 (fr) | 2005-12-16 | 2008-02-01 | Oreal | Composition cosmetique ou pharmaceutique comprenant un copolymere comportant au moins un groupe ionisable, et procede de traitement cosmetique |
| US20070190008A1 (en) | 2005-12-20 | 2007-08-16 | Catherine Campain | Process for permanently reshaping the hair, comprising applying to the hair at least one precipitated fixing polymer, and multi-compartment device |
| CN101395164A (zh) | 2006-01-10 | 2009-03-25 | 罗伊·J·于 | N-(膦酰基烷基)-氨基酸、其衍生物和组合物以及使用方法 |
| EP1847248A1 (de) | 2006-04-21 | 2007-10-24 | Schrader, Andreas, Dr. | Kosmetische Mittel zum Schutz oder zur Regenerierung des Haares oder der Haut |
| US20080066773A1 (en) | 2006-04-21 | 2008-03-20 | Anderson Daniel G | In situ polymerization for hair treatment |
| EP1880709A1 (en) | 2006-07-21 | 2008-01-23 | Wella Aktiengesellschaft | Method and composition for permanently shaping hair |
| GB0617024D0 (en) | 2006-08-30 | 2006-10-11 | Unilever Plc | Hair treatment compositions incorporating hair substantive polymers |
| US20100004391A1 (en) | 2006-11-17 | 2010-01-07 | David Mark Haddleton | Method for derivatizing hair with a reactive polyethylene glycol |
| FR2910275B1 (fr) | 2006-12-20 | 2010-06-04 | Oreal | Utilisation d'une silicone dans une composition de mise en forme des cheveux comprenant une alcoxysilane contenant un groupe fonctionnel solubilisant |
| WO2008092933A1 (de) | 2007-01-31 | 2008-08-07 | Basf Se | Kationische konditionierungsmittel |
| US20080187506A1 (en) | 2007-02-05 | 2008-08-07 | Jose Antonio Carballada | Hair care composition |
| US20080210253A1 (en) | 2007-02-05 | 2008-09-04 | Jose Antonio Carballada | Hair care composition |
| US20100111885A1 (en) | 2007-02-20 | 2010-05-06 | Shiseido Company, Ltd. | Hair-Shape Controlling Composition |
| JP2008303207A (ja) | 2007-05-07 | 2008-12-18 | Kao Corp | エーテルカルボキシレートの製造方法 |
| JP2009007283A (ja) | 2007-06-27 | 2009-01-15 | Lion Corp | 毛髪化粧料 |
| BRPI0813969B1 (pt) | 2007-07-03 | 2016-09-06 | Oreal | método para tingir permanentemente o cabelo, e, kit para tingir em substrato queratinoso. |
| US20090087398A1 (en) | 2007-08-20 | 2009-04-02 | Mark Anthony Brown | Method for Treating Damaged Hair |
| US20090053165A1 (en) | 2007-08-20 | 2009-02-26 | Mark Anthony Brown | Method for Treating Damaged Hair |
| US20140171354A1 (en) | 2007-10-18 | 2014-06-19 | Ecolab Usa Inc. | Detergent composition containing an amps copolymer and a maleic acid polymer |
| US7972388B2 (en) * | 2007-10-30 | 2011-07-05 | L'oreal S.A. | Methods and kits for maintaining the condition of colored hair |
| JP5496456B2 (ja) | 2007-12-28 | 2014-05-21 | 花王株式会社 | 毛髪化粧料 |
| FR2929508B1 (fr) * | 2008-04-08 | 2010-06-04 | Oreal | Procede de deformation permanente des fibres keratiniques presentant une etape de pretraitement acide |
| EP2113242A1 (en) | 2008-05-02 | 2009-11-04 | Pangaea Laboratories Limited | Antioxidant for use in cosmetic, medicated and pharmaceutical preparations |
| DE102008024030A1 (de) | 2008-05-16 | 2009-11-19 | Henkel Ag & Co. Kgaa | Aufhellmittel mit kationischen 3,4-Dihydroisochinoliniumderivaten, speziellen Alkanolaminen und Wasserstoffperoxid |
| DE102008002707A1 (de) * | 2008-06-27 | 2009-12-31 | Evonik Goldschmidt Gmbh | Haarbehandlungsmittel und Haarnachbehandlungsmittel zum Schutz vor Schäden durch chemische Behandlung und zur Reparatur bereits geschädigter Haare enthaltend als Wirksubstanzen Etherguanidine |
| JP2010065022A (ja) | 2008-08-12 | 2010-03-25 | Kao Corp | 毛髪処理用組成物 |
| FR2937640B1 (fr) | 2008-10-27 | 2011-02-25 | Oreal | Utilisation d'au moins un compose derive de lysine pour le conditionnement des fibres keratiniques, composition cosmetique le contenant et procede de conditionnement des fibres |
| BRPI0919999B1 (pt) | 2008-10-29 | 2017-03-07 | L' Oreal | processo e composição em gel para alisar ou relaxar cabelo |
| JP5411655B2 (ja) | 2008-12-03 | 2014-02-12 | 株式会社ミルボン | 毛髪処理方法及び毛髪処理剤 |
| US9421154B2 (en) | 2008-12-18 | 2016-08-23 | L'oreal | Composition and process for relaxing or straightening hair |
| FR2940102B1 (fr) | 2008-12-19 | 2016-03-11 | Oreal | Composition de teinture d'oxydation des fibres keratiniques comprenant un corps gras, un epaississant et un precurseur de colorant d'oxydation |
| FR2944441B1 (fr) | 2008-12-19 | 2012-02-17 | Oreal | Composition comprenant un corps gras et un actif hydrosoluble, procede de traitement la mettant en oeuvre |
| US20100158964A1 (en) | 2008-12-22 | 2010-06-24 | Corey Thomas Cunningham | Personal Care Composition Providing Quietness and Softness Enhancement and Articles Using the Same |
| US8163861B2 (en) * | 2009-01-15 | 2012-04-24 | Living Proof, Inc. | Beta-amino ester compounds and uses thereof |
| WO2010083368A2 (en) | 2009-01-16 | 2010-07-22 | Neocutis Sa | Calcium sequestration compositions and methods of treating skin pigmentation disorders and conditions |
| US20120022037A1 (en) | 2009-03-31 | 2012-01-26 | Kao Corporation | Aqueous hair cleansing agent |
| JP2010235523A (ja) | 2009-03-31 | 2010-10-21 | Kao Corp | 水性毛髪洗浄剤 |
| JP5866137B2 (ja) | 2009-04-30 | 2016-02-17 | ロレアル | アミノトリアルコキシシランまたはアミノトリアルケニルオキシシラン化合物を含む組成物を用いたヒトケラチン繊維の明色化および/または着色ならびに装置 |
| JP5653007B2 (ja) | 2009-06-12 | 2015-01-14 | ホーユー株式会社 | 毛髪処理剤組成物 |
| JP5670097B2 (ja) | 2009-06-19 | 2015-02-18 | 花王株式会社 | 二層分離型毛髪化粧料 |
| EP2277498A1 (en) * | 2009-07-22 | 2011-01-26 | KPSS-Kao Professional Salon Services GmbH | Composition and method for coulouring hair |
| DE102009044974A1 (de) | 2009-07-23 | 2011-01-27 | Henkel Ag & Co. Kgaa | Verwendung von Dihydroquercetin und mindestens einer Aminosäure zur positiven Beeinflussung des natürlichen Pigmentierungsprozesses |
| EP2295029A1 (en) | 2009-09-14 | 2011-03-16 | The Procter & Gamble Company | Method of chemically modifying the internal region of a hair shaft |
| FR2949970B1 (fr) | 2009-09-15 | 2011-09-02 | Oreal | Utilisation d'une huile siccative pour proteger la couleur vis-a-vis du lavage de fibres keratiniques teintes artificiellement ; procedes de coloration |
| US20120244082A1 (en) | 2009-12-18 | 2012-09-27 | Kao Germany Gmbh | Hair styling gel foam |
| JP2011170838A (ja) | 2010-01-20 | 2011-09-01 | Sanyo Electric Co Ltd | 画像処理装置及び電子機器 |
| JP2013528578A (ja) | 2010-04-28 | 2013-07-11 | ユニリーバー・ナームローゼ・ベンノートシヤープ | ヘアケア組成物 |
| FR2959917B1 (fr) | 2010-05-11 | 2012-07-27 | Oreal | Procede de traitement des cheveux |
| EP2387988B1 (en) | 2010-05-19 | 2017-09-27 | The Procter & Gamble Company | Oxidizing composition for the treatment of keratin fibres |
| US20110311463A1 (en) | 2010-06-16 | 2011-12-22 | Diamond George B | Hair spray and hair mousse with natural ingredients |
| JP5341029B2 (ja) | 2010-06-18 | 2013-11-13 | 花王株式会社 | 水性毛髪洗浄剤 |
| WO2012021472A2 (en) | 2010-08-09 | 2012-02-16 | L'oreal S. A. | Compositions and methods for sealing the surface of keratinous substrates |
| US9364420B2 (en) | 2010-08-18 | 2016-06-14 | Kao Usa Inc. | Hair conditioning compositions |
| WO2012029514A1 (ja) | 2010-08-31 | 2012-03-08 | 大塚製薬株式会社 | 頭皮頭髪洗浄用組成物 |
| EP2613760A2 (en) * | 2010-09-07 | 2013-07-17 | Segetis, Inc. | Compositions for dyeing keratin fibers |
| CN101966136A (zh) * | 2010-09-28 | 2011-02-09 | 广州温雅日用化妆品有限公司 | 一种直发染发方法 |
| CN102451117B (zh) | 2010-10-19 | 2016-04-06 | 花王株式会社 | 清洗剂组合物 |
| WO2012055811A1 (en) | 2010-10-26 | 2012-05-03 | L'oreal | Cosmetic composition comprising a fatty-chain alkoxysilane and a cationic or nonionic surfactant. |
| FR2966351B1 (fr) | 2010-10-26 | 2015-12-18 | Oreal | Composition cosmetique comprenant un alcoxysilane a chaine grasse, un agent tensioactif anionique et un agent tensioactif non ionique, amphotere ou zwitterionique. |
| FR2966352B1 (fr) | 2010-10-26 | 2016-03-25 | Oreal | Composition cosmetique comprenant un alcoxysilane a chaine grasse et un polymere cationique |
| US11406578B2 (en) | 2010-11-25 | 2022-08-09 | L'oreal | Process for stripping keratin fibres using a composition comprising a sulfinic acid derivative and an acidic aqueous composition |
| EP2460511A1 (en) | 2010-12-01 | 2012-06-06 | KPSS-Kao Professional Salon Services GmbH | Composition for the permanent shaping of human hair |
| WO2012075274A1 (en) | 2010-12-01 | 2012-06-07 | Isp Investments Inc. | Durable styling compositions and the uses thereof |
| KR101274668B1 (ko) * | 2010-12-06 | 2013-06-14 | 성균관대학교산학협력단 | 생체접착성이 우수한 온도 및 피에이치 민감성 스타형 블록 공중합체 및 이의 제조방법 그리고 이를 이용한 주사형 하이드로젤 약물전달체 |
| EP2651516B1 (en) | 2010-12-17 | 2017-06-14 | L'Oréal | Dye composition comprising a heterocyclic oxidation base and a 4-aminoindole coupler |
| DE102010064052A1 (de) | 2010-12-23 | 2012-06-28 | Henkel Ag & Co. Kgaa | Verfahren zur Umformung keratinhaltiger Fasern |
| EP2471504A1 (en) | 2010-12-28 | 2012-07-04 | KPSS-Kao Professional Salon Services GmbH | Two-part hair colouring composition |
| EP2561855B1 (en) | 2011-01-19 | 2017-10-11 | The Procter and Gamble Company | Method for chemically modifying the internal region of a hair shaft |
| EP2478892A1 (en) | 2011-01-19 | 2012-07-25 | The Procter & Gamble Company | Composition for chemically modifying the internal region of a hair shaft |
| FR2975900B1 (fr) | 2011-06-01 | 2015-02-20 | Oreal | Procede de traitement des fibres keratiniques defrisees |
| US9180086B2 (en) * | 2011-06-01 | 2015-11-10 | L'oreal | Process for treating straightened keratin fibres |
| FR2975901B1 (fr) | 2011-06-01 | 2014-12-05 | Oreal | Procede de traitement des fibres keratiniques defrisees |
| FR2975899B1 (fr) * | 2011-06-01 | 2015-03-06 | Oreal | Procede de traitement des fibres keratiniques defrisees |
| US20120329650A1 (en) | 2011-06-23 | 2012-12-27 | Agrinos AS | Agricultural Uses of HYTd |
| WO2013019969A2 (en) | 2011-08-03 | 2013-02-07 | Melaleuca, Inc. | Hair care compositions |
| WO2013029859A1 (de) | 2011-08-26 | 2013-03-07 | Henkel Ag & Co. Kgaa | Wasserstoffperoxid-haltige mittel mit verbesserter viskositätseinstellung |
| US20130118996A1 (en) | 2011-11-10 | 2013-05-16 | General Electric Company | Hexahydrotriazines, synthesis and use |
| DE102011086924A1 (de) | 2011-11-23 | 2013-05-23 | Henkel Ag & Co. Kgaa | Haarkonditionierende Mittel |
| TWI437027B (zh) | 2011-12-29 | 2014-05-11 | Ind Tech Res Inst | 一種含有軟鏈段之馬來醯亞胺聚合物及其製備方法 |
| FR2987742B1 (fr) * | 2012-03-09 | 2014-09-26 | Oreal | Procede de traitement pour la protection et la reparation des fibres keratiniques mettant en œuvre des polysaccharides oxydes |
| WO2013136480A1 (ja) | 2012-03-15 | 2013-09-19 | ホーユー株式会社 | 染毛剤及び染毛方法 |
| US9283156B2 (en) * | 2012-03-30 | 2016-03-15 | Zotos International, Inc. | Hair treatment and revitalizing composition and methods |
| US20130309190A1 (en) | 2012-05-15 | 2013-11-21 | L'oreal S.A. | Hair cosmetic and styling compositions based on maleic acid copolymers and polyamines |
| MX366321B (es) | 2012-06-01 | 2019-07-05 | Unilever Nv | Kit que comprende una composición acondicionadora de cabello y una composición activadora anhidra. |
| ITMI20121323A1 (it) | 2012-07-27 | 2014-01-28 | Giuliani Spa | Composizione farmaceutica o cosmeticaper il trattamento dell' alopecia |
| US9458414B2 (en) * | 2012-09-21 | 2016-10-04 | Gfbiochemicals Limited | Cleaning, surfactant, and personal care compositions |
| ES2796742T3 (es) | 2012-11-05 | 2020-11-30 | Hercules Llc | Composición que comprende un polímero de acondicionamiento y/o de peinado |
| FR2997846B1 (fr) | 2012-11-09 | 2023-10-20 | Oreal | Composition comprenant un derive dicarbonyle et un acide, le procede de lissage des fibres keratiniques a partir de cette composition |
| FR3001385B1 (fr) | 2013-01-31 | 2015-10-30 | Oreal | Composition comprenant un diacide carboxylique et une huile et procede de lissage des cheveux |
| ITMI20130218A1 (it) | 2013-02-18 | 2014-08-19 | Giuliani Spa | Composizione per uso cosmetico atta a produrre un effetto di pigmentazione dei capelli |
| ITMI20130555A1 (it) | 2013-04-09 | 2014-10-10 | Giuliani Spa | Composizione farmaceutica o cosmetica per contrastare l¿invecchiamento della pelle attraverso un¿azione antiinfiammatoria |
| DE102013209098A1 (de) | 2013-05-16 | 2014-11-20 | Henkel Ag & Co. Kgaa | transparente Blondiermittel mit Proteinen und/oder Silikonölen |
| CA2949933A1 (en) | 2013-06-26 | 2014-12-31 | L'oreal | Cosmetic composition for lightening or dyeing the hair, comprising two basic agents, an acid and an oxidizing agent |
| US9839600B2 (en) | 2013-06-28 | 2017-12-12 | L'oreal | Compositions and methods for treating hair |
| US9884004B2 (en) | 2013-06-28 | 2018-02-06 | L'oreal | Compositions and methods for treating hair |
| US20150037270A1 (en) | 2013-08-01 | 2015-02-05 | Liqwd, Inc. | Compositions and Kits for Hair and Skin |
| UA116148C2 (uk) | 2013-08-01 | 2018-02-12 | Ліквд, Інк. | Способи відновлення волосся і шкіри |
| US20150034119A1 (en) | 2013-08-01 | 2015-02-05 | Liqwd, Inc. | Hair Color Smoothing Compositions and Methods |
| US9095518B2 (en) | 2013-08-01 | 2015-08-04 | Liqwd, Inc. | Methods for fixing hair and skin |
| CA2918829A1 (en) | 2013-08-23 | 2015-02-26 | The Procter & Gamble Company | Hair colouring methods and kits thereof |
| EP3036009A1 (en) | 2013-08-23 | 2016-06-29 | The Procter & Gamble Company | Hair colouring methods and kits thereof |
| WO2015033351A1 (en) * | 2013-09-06 | 2015-03-12 | Jubilant Life Sciences Limited | Anti-dandruff compositions and hair care formulations containing zinc pyrithione and quaternary ammonium salt |
| EP2857003A1 (en) | 2013-10-02 | 2015-04-08 | The Procter and Gamble Company | Hair conditioning composition comprising ammonium thioglycolate and/or ammonium thiolactate |
| WO2015058942A1 (en) | 2013-10-25 | 2015-04-30 | Unilever N.V. | A liquid disinfecting composition |
| JP2015086211A (ja) | 2013-10-29 | 2015-05-07 | 有限会社岡田技研 | 毛髪保護剤および毛髪化粧料 |
| KR20160077206A (ko) | 2013-11-08 | 2016-07-01 | 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 | 반-영구적으로 모발을 펴는 조성물 및 방법 |
| US20160303013A1 (en) | 2013-11-21 | 2016-10-20 | Conopco, Inc., D/B/A Unilever | Method of treating hair |
| GB201402257D0 (en) | 2014-02-10 | 2014-03-26 | Revolymer Ltd | Novel Peracid - containing particle |
| US20150283041A1 (en) | 2014-04-02 | 2015-10-08 | L'oreal | Compositions for altering the appearance of hair |
| MX389718B (es) | 2014-05-16 | 2025-03-20 | Olaplex Inc | Formulaciones y metodos de tratamiento con queratina. |
| JP6448079B2 (ja) | 2014-06-13 | 2019-01-09 | 互応化学工業株式会社 | 化粧料組成物 |
| DE102014213325A1 (de) | 2014-07-09 | 2016-01-14 | Henkel Ag & Co. Kgaa | Verbesserte Entfärbung von gefärbten keratinischen Fasern |
| DE102014213317A1 (de) | 2014-07-09 | 2016-01-14 | Henkel Ag & Co. Kgaa | Verbesserte Entfärbung von gefärbten keratinischen Fasern |
| DE102014213318A1 (de) | 2014-07-09 | 2016-01-14 | Henkel Ag & Co. Kgaa | Verbesserte Entfärbung von gefärbten keratinischen Fasern |
| EP3015135B1 (en) | 2014-10-29 | 2020-09-09 | Noxell Corporation | Hair colouration with a cationic or anionic coloured polymer, method and kit thereof |
| KR101922543B1 (ko) | 2014-11-28 | 2018-11-28 | (주)아모레퍼시픽 | 말레산을 유효성분으로 포함하는 모발용 화장료 조성물 |
| FR3029776B1 (fr) | 2014-12-10 | 2019-11-29 | L'oreal | Composition anhydre sous forme d'aerosol comprenant un actif anti-transpirant, un polymere ethylenique filmogene non hydrosoluble et sequence et une silicone phenylee |
| DE102014225545A1 (de) | 2014-12-11 | 2016-06-16 | Henkel Ag & Co. Kgaa | "Verbesserte Entfärbung von gefärbten keratinischen Fasern" |
| WO2016100885A1 (en) | 2014-12-19 | 2016-06-23 | L'oreal | Hair cosmetic composition |
| US20160175238A1 (en) | 2014-12-19 | 2016-06-23 | L'oreal | Hair cosmetic composition containing a polyurethane latex polymer and a silicone-organic polymer compound |
| FR3030240B1 (fr) | 2014-12-23 | 2017-07-28 | Oreal | Procede de traitement des fibres keratiniques avec une composition comprenant un acide amine |
| GB201501583D0 (en) | 2015-01-30 | 2015-03-18 | Univ Strathclyde | Uses of co-crystals |
| WO2016161360A1 (en) | 2015-04-03 | 2016-10-06 | Nutech Ventures | Effective hair styling compositions and processes |
| US9597273B2 (en) | 2015-04-24 | 2017-03-21 | Liqwd, Inc. | Methods for treating relaxed hair |
| JP2018514570A (ja) | 2015-05-01 | 2018-06-07 | ロレアル | 化学処理における活性剤の使用 |
| DE102015208788A1 (de) | 2015-05-12 | 2016-11-17 | Henkel Ag & Co. Kgaa | Mittel zur schonenden oxidativen Aufhellung von keratinhaltigen Fasern |
| DE102015210751A1 (de) | 2015-06-12 | 2016-12-15 | Henkel Ag & Co. Kgaa | Emulsionen zur verbesserten reduktiven Entfärbung keratinischer Fasern |
| US10568823B2 (en) | 2015-07-10 | 2020-02-25 | Hercules Llc | Method of strengthening hair fibers and protecting dyed hair color from fading or wash-out |
| US10398914B2 (en) | 2015-09-08 | 2019-09-03 | Kao Germany Gmbh | Process for treating hair |
| US10632053B2 (en) | 2015-09-08 | 2020-04-28 | Kao Germany Gmbh | Process for bleaching hair |
| WO2017041909A1 (en) | 2015-09-08 | 2017-03-16 | Kao Germany Gmbh | Process for treating hair |
| US11110041B2 (en) | 2015-09-08 | 2021-09-07 | Kao Germany Gmbh | Process for permanent shaping hair |
| US10398634B2 (en) | 2015-09-08 | 2019-09-03 | Kao Germany Gmbh | Process for oxidative dyeing hair |
| EP3346972B1 (en) | 2015-09-08 | 2021-05-26 | Kao Germany GmbH | Process for treating hair |
| BR112018004644B1 (pt) | 2015-09-08 | 2021-06-01 | Kao Germany Gmbh | Processo para alisamento semipermanente e modelagem permanente do cabelo e kit |
| CN105267066B (zh) | 2015-10-08 | 2019-06-11 | 知识产权全资有限公司 | 用于处理头发的方法及其试剂盒 |
| DE102015221460B4 (de) | 2015-11-03 | 2022-11-10 | Henkel Ag & Co. Kgaa | Dauerwellverfahren mit verbesserter Pflegeleistung und Wellwirkung |
| DE102015222216A1 (de) | 2015-11-11 | 2017-05-11 | Henkel Ag & Co. Kgaa | Reduktiver Farbabzug mit Sulfinsäure-Derviaten in Pastenform |
| DE102015222214A1 (de) | 2015-11-11 | 2017-05-11 | Henkel Ag & Co. Kgaa | Verbesserte Entfärbung von gefärbten keratinischen Fasern |
| JP6834376B2 (ja) | 2015-11-17 | 2021-02-24 | 日油株式会社 | 界面活性剤組成物 |
| EP3377030B1 (de) | 2015-11-20 | 2020-05-06 | Henkel AG & Co. KGaA | Haar schonende mittel und verfahren zur oxidativen haarfärbung oder blondierung |
| DE102015223196A1 (de) | 2015-11-24 | 2017-05-24 | Henkel Ag & Co. Kgaa | Mittel und Verfahren zur Reinigung und/oder zur Pflege geschädigter keratinischer Fasern |
| JP6873994B2 (ja) | 2015-11-24 | 2021-05-19 | ロレアル | 毛髪を処置するための組成物 |
| EP3380062B1 (en) | 2015-11-24 | 2021-07-07 | L'oreal | Compositions for treating the hair |
| CN108495686A (zh) | 2015-11-24 | 2018-09-04 | 欧莱雅 | 用于处理毛发的组合物 |
| JP6882315B2 (ja) | 2015-11-24 | 2021-06-02 | ロレアル | 毛髪を処置するための組成物 |
| DE102015223829A1 (de) | 2015-12-01 | 2017-06-01 | Henkel Ag & Co. Kgaa | Leistungsstarke Haarbehandlungsmittel mit Anti-Auswasch-Effekt |
| DE102015223828A1 (de) | 2015-12-01 | 2016-09-15 | Henkel Ag & Co. Kgaa | Leistungsstarke Haarbehandlungsmittel mit Anti-Auswasch-Effekt |
| DE102015223817A1 (de) | 2015-12-01 | 2017-06-01 | Henkel Ag & Co. Kgaa | Leistungsstarke Haarbehandlungsmittel mit strukturstärkendem-Effekt |
| DE102015223840A1 (de) | 2015-12-01 | 2017-06-14 | Henkel Ag & Co. Kgaa | Leistungsstarke Haarbehandlungsmittel mit Anti-Auswasch-Effekt |
| DE102015223820A1 (de) | 2015-12-01 | 2017-06-01 | Henkel Ag & Co. Kgaa | "Leistungsstarke Haarbehandlungsmittel mit strukturstärkendem-Effekt" |
| DE102015223832A1 (de) | 2015-12-01 | 2017-06-01 | Henkel Ag & Co. Kgaa | Leistungsstarke Haarbehandlungsmittel mit Anti-Auswasch-Effekt |
| WO2017096154A1 (en) | 2015-12-04 | 2017-06-08 | The Procter & Gamble Company | Hair care regimen using compositions comprising moisture control materials |
| DE102015225137A1 (de) | 2015-12-14 | 2017-06-14 | Henkel Ag & Co. Kgaa | Oxidationsmittel zur oxidativen Färbe- und Blondierbehandlung keratinischer Fasern mit reduzierter Schädigung |
| FR3044904B1 (fr) | 2015-12-14 | 2019-05-31 | L'oreal | Composition comprenant l'association d'alcoxysilanes particuliers et d'un tensioactif |
| DE102015225895A1 (de) | 2015-12-18 | 2017-06-22 | Henkel Ag & Co. Kgaa | Spezielle Oxidationsmittelzubereitungen und Verfahren zur oxidativen Farbänderung von keratinischen Fasern |
| DE102016200688A1 (de) | 2016-01-20 | 2017-07-20 | Henkel Ag & Co. Kgaa | Keratinfaserschonende Mittel und Verfahren zur oxidativen Haarfärbung |
| CN105902404A (zh) | 2016-06-14 | 2016-08-31 | 知识产权全资有限公司 | 强发成分以及强发的方法 |
| CN105902403A (zh) | 2016-05-19 | 2016-08-31 | 知识产权全资有限公司 | 强发成分以及强发的方法 |
| DE102016209471A1 (de) | 2016-05-31 | 2017-11-30 | Henkel Ag & Co. Kgaa | Blondiermittel und Verfahren zur schonenden oxidativen Haaraufhellung I |
| CN106265109A (zh) | 2016-08-22 | 2017-01-04 | 知识产权全资有限公司 | 强发成分以及强发并使头发具有极佳手感的方法 |
| US20180055751A1 (en) | 2016-08-31 | 2018-03-01 | L'oreal | Compositions comprising an associaton of cationic compounds, silane compounds, esters and fatty substances |
| US20180116942A1 (en) | 2016-10-31 | 2018-05-03 | L'oreal | Compositions for chemically treated hair |
| WO2018085478A1 (en) | 2016-11-02 | 2018-05-11 | L'oreal | Hair lightening compositions and methods of use |
| US11135150B2 (en) | 2016-11-21 | 2021-10-05 | L'oreal | Compositions and methods for improving the quality of chemically treated hair |
| US20180140532A1 (en) | 2016-11-21 | 2018-05-24 | L'oreal | Compositions and methods for restructuring chemically treated hair |
| US10004673B1 (en) | 2017-02-08 | 2018-06-26 | L'oreal | Hair treatment composition comprising Michael addition product and methods for treating hair |
| US9918923B1 (en) | 2017-02-28 | 2018-03-20 | L'oreal | Leave-on hair styling compositions and methods of use |
| US20180280267A1 (en) | 2017-03-31 | 2018-10-04 | L'oreal | Kits and methods for treating hair |
| WO2018183880A1 (en) | 2017-03-31 | 2018-10-04 | L'oreal | Methods for treating hair |
| WO2018183858A1 (en) | 2017-03-31 | 2018-10-04 | L'oreal | Hair-treatment compositions |
| US20180280271A1 (en) | 2017-03-31 | 2018-10-04 | L'oreal | Kits and methods for treating hair |
| US10561599B2 (en) | 2017-05-24 | 2020-02-18 | L'oreal | Methods and kits for treating chemically relaxed hair |
| US10576307B2 (en) | 2017-05-24 | 2020-03-03 | L'oreal | Hair-treatment compositions, methods, and kits for treating hair |
| US11433011B2 (en) | 2017-05-24 | 2022-09-06 | L'oreal | Methods for treating chemically relaxed hair |
| EP4011355A1 (en) | 2017-12-29 | 2022-06-15 | L'oreal | Compositions for altering the color of hair |
| US11090249B2 (en) | 2018-10-31 | 2021-08-17 | L'oreal | Hair treatment compositions, methods, and kits for treating hair |
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| JP2018535233A (ja) | 2018-11-29 |
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| CN108495613A (zh) | 2018-09-04 |
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| US10441518B2 (en) | 2019-10-15 |
| EP3380062B1 (en) | 2021-07-07 |
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| B21F | Lapse acc. art. 78, item iv - on non-payment of the annual fees in time |
Free format text: REFERENTE A 8A ANUIDADE. |
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| B24J | Lapse because of non-payment of annual fees (definitively: art 78 iv lpi, resolution 113/2013 art. 12) |
Free format text: EM VIRTUDE DA EXTINCAO PUBLICADA NA RPI 2802 DE 17-09-2024 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDA A EXTINCAO DA PATENTE E SEUS CERTIFICADOS, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013. |