JP2006527744A5 - - Google Patents

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JP2006527744A5
JP2006527744A5 JP2006516303A JP2006516303A JP2006527744A5 JP 2006527744 A5 JP2006527744 A5 JP 2006527744A5 JP 2006516303 A JP2006516303 A JP 2006516303A JP 2006516303 A JP2006516303 A JP 2006516303A JP 2006527744 A5 JP2006527744 A5 JP 2006527744A5
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dye
composition according
optionally substituted
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cationic
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JP4728230B2 (en
JP2006527744A (en
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Priority claimed from FR0307186A external-priority patent/FR2855967B1/en
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適切な染色媒体中に、酸化剤、7より大きいpHを達成する量でのアルカリ剤、及びリンカーを介して共に結合されたいくつかの発色団を含むカチオン性混合染料を含む明色化染料組成物であって、前記発色団の少なくとも二つは異なり、前記発色団は400から800nmの間の少なくとも一つの吸収最大を示す組成物。   Lightening dye composition comprising an oxidizing agent, an alkaline agent in an amount to achieve a pH greater than 7 and a cationic mixed dye comprising several chromophores bonded together through a linker in a suitable dyeing medium A composition wherein at least two of the chromophores are different and the chromophore exhibits at least one absorption maximum between 400 and 800 nm. 前記発色団が、アゾ、キサンテン、ヒドラゾン及びアリールヒドラゾン、フェノチアジン、アクリジン、ジケトピロロピロール、シアニン、特にテトラアザカルボシアニン、アントラキノン、メチン、アゾメチン、インジゴ、及びニトロ、特にニトロ(ヘテロ)芳香族、の各発色団から選択される、請求項に記載の組成物。 The chromophore is azo, xanthene, hydrazone and arylhydrazone, phenothiazine, acridine, diketopyrrolopyrrole, cyanine, especially tetraazacarbocyanine, anthraquinone, methine, azomethine, indigo, and nitro, especially nitro (hetero) aromatic, It is selected from the chromophore composition of claim 1. 前記混合染料がジカチオン性である、請求項1または2に記載の組成物。 The composition according to claim 1 or 2 , wherein the mixed dye is dicationic. 前記混合染料が2または3の発色団を含み、発色団の少なくとも二つがカチオン性であり、リンカーがカチオン性または非カチオン性である、請求項1または2に記載の組成物。 The composition according to claim 1 or 2 , wherein the mixed dye comprises 2 or 3 chromophores, at least two of the chromophores are cationic and the linker is cationic or non-cationic. 前記混合染料が、式:染料1-L-染料2[式中、Lはカチオン性または非カチオン性リンカーであり、染料1及び染料2は異なるカチオン性発色団である]に対応する、請求項1からのいずれか一項に記載の組成物。 The mixed dye corresponds to the formula: Dye 1-L-Dye 2, wherein L is a cationic or non-cationic linker and Dye 1 and Dye 2 are different cationic chromophores. The composition according to any one of 1 to 4 . 前記混合染料が、カチオン性アゾ発色団を含む、請求項1からのいずれか一項に記載の組成物。 The composition according to any one of claims 1 to 5 , wherein the mixed dye comprises a cationic azo chromophore. 前記リンカーが、C−C 、直鎖状、分枝状、または環状の、任意に置換された炭化水素ベースの鎖であって、前記鎖の炭素原子の一つ以上は、硫黄、窒素、または酸素のような少なくとも一つのヘテロ原子で、及び/またはカルボニル基のようなヘテロ原子を含む少なくとも一つの基で置換されても良く、前記炭化水素ベースの鎖は、不飽和であるか、少なくとも一つの任意に置換されたアルケニル基;任意に置換されたアリーレン基;任意に置換された二価テレフタルアミド基;任意に置換された二価複素環基、たとえば二価トリアジン基、または-NH-CO-基を含んでも良いものから選択される、請求項1からのいずれか一項に記載の組成物。 Wherein the linker is a C 1 -C 2 0, linear, branched, or cyclic, a hydrocarbon-based chain, optionally substituted, one or more carbon atoms of the chain, sulfur May be substituted with at least one heteroatom such as nitrogen, or oxygen and / or with at least one group containing a heteroatom such as a carbonyl group, the hydrocarbon-based chain being unsaturated Or at least one optionally substituted alkenyl group; an optionally substituted arylene group; an optionally substituted divalent terephthalamide group; an optionally substituted divalent heterocyclic group such as a divalent triazine group; or 7. A composition according to any one of claims 1 to 6 , selected from those which may contain -NH-CO- groups. 前記リンカーが、前記混合染料が有している発色団の吸収最大の波長のスケール上の位置が、別個に採取される発色団のそれぞれの吸収最大に対して30ナノメーターより大きいものまで変更されるべきではない態様で、前記混合染料から発色団のそれぞれを引き離す原子または原子群を含む、請求項1からのいずれか一項に記載の組成物。 The linker is changed so that the position of the absorption maximum wavelength of the chromophore of the mixed dye on the scale is greater than 30 nanometers for each absorption maximum of the separately collected chromophores. 8. A composition according to any one of claims 1 to 7 comprising atoms or groups of atoms that separate each of the chromophores from the mixed dye in a manner that should not. 前記混合染料が下式:
Figure 2006527744
[式中、Lはリンカーであり、R1及びR1’は、一つ以上のヒドロキシルで任意に置換された好ましくはC-Cのアルキル基、C-Cアルコキシ、C-C(ポリ)ヒドロキシアルコキシ、アミノ、C-C(ジ)アルキルアミノ、または任意に置換されたアリール基から独立に選択され、R2及びR2’は、一つ以上のヒドロキシルで任意に置換されたC-Cアルキル基、C-Cアルコキシ、C-C(ポリ)ヒドロキシアルコキシ、アミノ、またはC-C(ジ)アルキルアミノ基;任意に置換されたフェニル基から独立に選択され、Anは、一つ以上の同一または異なる、一価または多価のアニオンを表す]。
に対応する、請求項1からのいずれか一項に記載の組成物。
The mixed dye has the following formula:
Figure 2006527744
Wherein L is a linker and R 1 and R 1 ′ are preferably C 1 -C 6 alkyl groups, C 1 -C 2 alkoxy, C 2 -C 4 , optionally substituted with one or more hydroxyls. Independently selected from (poly) hydroxyalkoxy, amino, C 1 -C 2 (di) alkylamino, or an optionally substituted aryl group, R 2 and R 2 ′ are optionally substituted with one or more hydroxyls C 1 -C 6 alkyl group, C 1 -C 2 alkoxy, C 2 -C 4 (poly) hydroxyalkoxy, amino, or C 1 -C 2 (di) alkylamino group; independent of an optionally substituted phenyl group And An represents one or more of the same or different monovalent or polyvalent anions.
Corresponding to composition according to any one of claims 1 to 8.
前記混合染料が以下の構造:
Figure 2006527744
Figure 2006527744
に対応する、請求項に記載の組成物。
The mixed dye has the following structure:
Figure 2006527744
Figure 2006527744
The composition according to claim 8 , corresponding to
前記混合染料の量が、前記組成物の総重量に対して0.001%から20%の間である、請求項1から1のいずれか一項に記載の組成物。 Wherein the amount of mixed dye is said is between 0.001% to 20% relative to the total weight of the composition A composition according to any one of 0 claims 1 1. pHが8から11の間である、請求項1から1のいずれか一項に記載の組成物。 The composition according to any one of claims 1 to 11, wherein the pH is between 8 and 11. 請求項1から12のいずれか一項に記載の染料組成物が、明色化及び所望の着色を得るのに十分な時間でケラチン繊維に適用されることを特徴とする、ケラチン繊維の酸化染色方法。 Oxidative dyeing of keratin fibers, characterized in that the dye composition according to any one of claims 1 to 12 is applied to keratin fibers in a time sufficient to obtain lightening and the desired coloration. Method. 前記酸化剤が、請求項1から13のいずれか一項に規定された混合染料を含むものとは異なる組成物に含まれる、請求項13に記載の方法。 The oxidant is included in different compositions intended to include a defined mixed dye to any one of claims 1 to 13, The method of claim 13. 第一の区画がアルカリ化剤と請求項1から1に規定された混合染料とを含む染料組成物を含み、第二の区画が酸化剤を含む、多区画装置。 Comprising a dye composition comprising a mixture dye first compartment is defined by claim 1 with an alkali agent to 1 1, the second compartment contains an oxidizing agent, multi-compartment device. ケラチン繊維を明色化染色するための、請求項1から1に規定された染料の使用。 Keratin fibers for dyeing lightening, the use of defined dye claims 1 to 1 2. 良好なシャンプー耐性を得るための、請求項16に記載の使用。 Use according to claim 16 , for obtaining good shampoo resistance. 経時的な着色の良好な耐性を得るための、請求項16に記載の使用。 Use according to claim 16 , for obtaining good resistance to coloration over time. 経時的に安定な染料組成物を得るための、請求項16に記載の使用。 Use according to claim 16 , for obtaining a dye composition which is stable over time.
JP2006516303A 2003-06-16 2004-06-16 Brightening dyeing composition comprising at least one cationic direct dye having a mixed chromophore Expired - Fee Related JP4728230B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR0307186A FR2855967B1 (en) 2003-06-16 2003-06-16 LIGHTENING TINCTORIAL COMPOSITION COMPRISING AT LEAST ONE MIXED CHROMOPHORES CATIONIC DIRECT DYE
FR03/07186 2003-06-16
PCT/FR2004/001517 WO2004112738A1 (en) 2003-06-16 2004-06-16 Tinctorial brightener composition containing at least one directly cationic colorant having mixed chromophores

Publications (3)

Publication Number Publication Date
JP2006527744A JP2006527744A (en) 2006-12-07
JP2006527744A5 true JP2006527744A5 (en) 2007-08-02
JP4728230B2 JP4728230B2 (en) 2011-07-20

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EP (1) EP1648402A1 (en)
JP (1) JP4728230B2 (en)
KR (1) KR20060021898A (en)
CN (1) CN1835730B (en)
BR (1) BRPI0411495A (en)
FR (1) FR2855967B1 (en)
MX (1) MXPA05013749A (en)
WO (1) WO2004112738A1 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2895904B1 (en) * 2006-01-12 2008-02-29 Oreal USE FOR COLORING WITH THE LIGHTENING EFFECT OF KERATINIC MATERIALS OF A COMPOSITION COMPRISING A CYANINE-LIKE FLUORESCENT DYE
JP2008105976A (en) * 2006-10-24 2008-05-08 Shinichiro Isobe Cosmetic composition
CN107635537A (en) * 2015-03-19 2018-01-26 诺赛尔股份有限公司 For the composition dyed using cation direct dye to hair
CN107635538A (en) * 2015-03-19 2018-01-26 诺赛尔股份有限公司 Use the method for direct dyes compound dyed hair
US9849072B2 (en) 2015-03-19 2017-12-26 Noxell Corporation Method of coloring hair with direct dye compounds
CN107750154A (en) * 2015-03-19 2018-03-02 诺赛尔股份有限公司 For the composition dyed using cation direct dye to hair
US10034823B2 (en) 2016-09-16 2018-07-31 Noxell Corporation Method of coloring hair with washfast blue imidazolium direct dye compounds
US9918919B1 (en) 2016-09-16 2018-03-20 Noxell Corporation Method of coloring hair with washfast yellow imidazolium direct dye compounds

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2215944T3 (en) * 1994-11-03 2004-10-16 Ciba Specialty Chemicals Holding Inc. CATIONIC IMIDAZOLAZOIC COLORS.
FR2773991B1 (en) * 1998-01-26 2000-05-26 Oreal USE AS A PROTECTIVE AGENT FOR KERATINIC FIBERS OF HETEROCYCLIC QUATERNARY POLYAMMONIUM POLYMERS AND COSMETIC COMPOSITIONS
JP2002080332A (en) * 2000-03-17 2002-03-19 Kao Corp Hair dye composition
JP2001261535A (en) * 2000-03-17 2001-09-26 Kao Corp Hair dyeing agent composition
EP1133975B1 (en) * 2000-03-17 2008-02-13 Kao Corporation Use of a compound for dyeing hair
BR0114585A (en) * 2000-10-12 2003-08-26 Ciba Sc Holding Ag Cationic Imidazole Azo-Dyes
FR2822697B1 (en) * 2001-04-02 2003-07-25 Oreal NEW DYE COMPOSITION FOR DYEING KERATIN FIBERS COMPRISING A PARTICULAR CATIONIC AZO DYE
FR2822693B1 (en) * 2001-04-02 2003-06-27 Oreal NOVEL TINCTORIAL COMPOSITION FOR DYEING KERATINIC FIBERS COMPRISING A PARTICULAR CATIONIC AZO DYE
FR2822698B1 (en) * 2001-04-03 2006-04-21 Oreal NEW DYE COMPOSITION FOR DYEING KERATIN FIBERS COMPRISING A DICATIONIC MONOAZO DYE
FR2825625B1 (en) * 2001-06-12 2005-06-17 Oreal USE OF DICATIONIC COMPOUNDS IN DYEING OF HUMAN KERATIN FIBERS AND COMPOSITIONS CONTAINING SAME
EP1404762B1 (en) * 2001-07-11 2009-11-25 Basf Se A method of coloring hair using cationic dyes

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