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JPH0219576A - 角質繊維染色組成物 - Google Patents

角質繊維染色組成物

Info

Publication number
JPH0219576A
JPH0219576A JP63169571A JP16957188A JPH0219576A JP H0219576 A JPH0219576 A JP H0219576A JP 63169571 A JP63169571 A JP 63169571A JP 16957188 A JP16957188 A JP 16957188A JP H0219576 A JPH0219576 A JP H0219576A
Authority
JP
Japan
Prior art keywords
substance
dyeing composition
coupling
dyeing
hair
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP63169571A
Other languages
English (en)
Other versions
JP2526099B2 (ja
Inventor
Jiro Kawase
川瀬 次朗
Tsutomu Mano
真野 勉
Michio Obayashi
大林 道夫
Daisuke Misu
大介 三栖
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kao Corp
Original Assignee
Kao Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kao Corp filed Critical Kao Corp
Priority to JP63169571A priority Critical patent/JP2526099B2/ja
Publication of JPH0219576A publication Critical patent/JPH0219576A/ja
Application granted granted Critical
Publication of JP2526099B2 publication Critical patent/JP2526099B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/10Preparations for permanently dyeing the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/347Phenols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4906Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
    • A61K8/4926Cosmetics 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/494Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
    • A61K8/4953Cosmetics 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Coloring (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。

Description

【発明の詳細な説明】 c座業上の利用分野〕 本発明は染色組成物に関し、更に詳細には毛受等の角質
繊維を高彩度に染色することができる角質繊維染色組成
物に関する。
〔従来の技術〕
毛髪等の角質繊維の染色には、従来よシ顕色吻質とカツ
プリング物質を組み合せて用いる、いわゆる酸化染色剤
が広く使用されている。この酸化染色剤は顕色物質とカ
ツプリング物質の酸化カッfリングによって生じる、い
わゆる酸化色素が毛髪等を強く染色することを利用した
ものでめる。そして顕色物質としては、一般にp−フェ
ニレンシアミン誘導体、p−アミンフェノール銹導体、
シアミノビリシン誘導体、4−7ミノビラゾロン誘導体
、複素環状ヒドラゾン等が使用されている。
〔発明が解決しようとする課題〕
しかしながら、従来の酸化染色剤は、彩度、染着力およ
び盛ろう性において未だ満足すべきものではなかった。
〔課題を解決するための手段〕
そこで本発明者らは前記問題点を解決すべく種々検討を
重ねた結果、顕色物質として特定のトリアミノビリミシ
ン誘導体を使用することによシ、角質繊維を高彩度で強
い色調に染色することが可能となり、かつその染色は優
れた堅ろう性を有することを見出し、本発明を完成した
すなわち、本発明は顕色物質およびカップリング物質を
含有する染色組成物において、顕色物質が、次の一般式
(I)または(1′)で表わされるトリアミノピリミジ
ン誘導体く以下化合’II!l (I)と称する)であ
ることを特徴とする角質繊維染色組成物を提供するもの
である。
本発明に使用される化合物(1)の塩としては、塩酸、
硫酸、リン酸等の無機酸または、炭素数1〜20の直鎖
もしくは分岐アルキル基を有するカルメン酸、ヒドロキ
シカルボン酸、−リヒドロキシカルボン嫉、スルホン酸
等の有機酸が挙げられ、塩酸、硫酸、リン酸、酢酸、プ
ロピオン酸、乳酸、クエン酸等が好ましい。
本発明染色組成物に使用されるカップリング物質として
は、通常酸化染毛剤に慣用されているものであれば特に
制限されないが、例えばα−す7トール、0−クレゾー
ル、 m −クレゾール、2,6−ジメチルフェノール
、2.5−ジメチルフェノール、3,4−ジメチルフェ
ノール、3,5−ジメチルフェノール、ベンズカテキン
、ピロガロール、1.5−ジヒドロキシナフタレン、1
,7−ジヒドロキシナフタレン、5−アミノ−2−メチ
ルフェノール、ヒドロキノン、2,4−ゾアミノアニン
ール、m−トルイレンシアミン、4−アミンフェノール
、レゾルシン、レゾルシンモノメチルエーテル、m−フ
ェニレンシアミン、1−フェニル−3−)fルー5−ピ
ラゾロン、1−フェニル−3−アミノ−5−ピラゾロン
、1−フェニル−3,5−ゾケトービラゾリゾン、1−
メチル−7−ゾメチル−アミノ−4−ヒドロキシキノロ
ン−2,1−アミノ−3−アセチル−アセトアミノ−4
−二トロベンゾール、1−アミノ−3−シアンアセチル
−アミノ−4−ニトロ−ペンゾール、m−アミンフェノ
ール、4−クロロレゾルシン、2−メチルレゾルシン、
2.4−Pアミノフェノキシエタノール、2,6−ジア
ミノビリジン、3,5−シアミノ−トリフロロメチルベ
ンゼン、2,4−シアミノ−フロロベンゼン、3.5−
シアミノ−フロロベンゼン、2.4−シアミノ−6−ヒ
ドロキシピリミジン、2,4.6−トリアミノビリミシ
ン、2−アミノ−4,6−ジヒドロキシピリミジン、4
−アミノ−2,6−ジヒドロキシビリミジン、4,6−
ゾアミノー2−ヒドロキシピリミジン、p−ニトロ−〇
−フェニレンシアミン、2−アミノ−5−ニトロフェノ
ール、p−ニトロ−m−フェニレンシアミン、〇−二ヒ
トローp−フェニレンシアミン2−アミノ−4−ニトロ
フェノール等が挙げられる。
本発明に使用される顕色物質は、レゾルシン系のカップ
リング物質と組み合せることによシ高彩度の赤系色調が
得られ、特にレゾルシン、2−メチルレゾルシン、4−
クロロレゾルシンをカップリング物質とすると、高彩度
のオレンゾル赤の色調が得られる。また、本発明に使用
される顕色物質を、シアミノビリシン系のカップリング
物質と組み合わせることによシアざやかな黄色が得られ
、特に4−ゾロビル−2,6−ジアミノピリジン、3゜
4−ジメチル−2,6−ゾアミノビリジンをカップリン
グ物質として用いると高彩度の黄色が得られる。
本発明の染色組成物中の顕色物質とカップリング物質の
配合割合は、一方の成分が他方に比べ過剰となっていて
もさしつかえないが、モル比で1:0.5〜1:2程度
であることが好ましい。また顕色物質およびカップリン
グ物質は、ともに単独でも二櫨以上を組み合せても使用
することができる。
また本発明の染色組成物には所望の色調を得るため必要
でめれば、更に公知の顕色物質、通常の1染性染料等を
配合することができる。
本発明染色組成物は、空気中の酸素によっても酸化カッ
プリングを生起し、毛髪等を染色するが、化学的酸化剤
を添加することによシ酸化カツプリングを生起させるの
が好ましい。特に好ましい酸化剤としては、過酸化水素
:過酸化水素が尿素、メラミン又は5!IrIRナトリ
ウムに付加した生成物;このような過酸化水素付加物と
過酸化カリウムー二硫酸との混合物等が挙げられる。
本発明の染色組成物は通常、クリーム、エマルション、
グル、溶液等の剤型で提供されるのが好ましい。このよ
うな剤型とするには、前記顕色物質およびカップリング
物質に、通常化粧品分野において用いられる湿潤剤(乳
化剤)、可溶化剤、増粘剤、安定化剤、感触向上剤、整
髪基剤、香料等を添加し、常法に従って製造すればよい
。ここで用いられる湿調剤(乳化剤)としては、例えば
アルキルベンゼンスルホネート、脂肪アルコールサルフ
ェート、アルキルスルホネート、脂肪酸アルカノールア
ミド、エチレンオキシドと脂肪アルコールとの付加生成
物等が挙げられる。また増粘剤としては、例えばメチル
セルロース、デンプン、高級脂肪アルコール、ノQラフ
イン油、脂肪酸等が挙げられ、安定化剤としては、例え
ば亜硫酸塩等の還元剤、ヒドロキノン酵導体、キレート
剤等が挙げられ、感触向上剤、整髪基剤としては、例え
ばシリコーン、高級アルコール、各種非イオン界面活性
剤等の油剤、各種のカチオンビリマー等が挙げられる。
これらの剤をにおける顕色物質とカップリング物質の配
合量は、合計で0.2〜5重童チ(以下単にチで示す)
、特に1〜3チが好ましい。湿潤剤(乳化剤)は通常0
.5〜30チ、増粘剤は0.1〜25チ配合されるのが
好ましい。
またこれらの剤槃において、組成物全体の−は8〜10
程度に調整されるのが好ましい。
本発明染色組成物を用いて角質繊維の染色を実施するに
は、例えば本発明染色組成物に酸化剤を添加して酸化カ
ップリングを行い染色液を調製し、この染色液を角質繊
維に適用し、10〜50分、好ましくは25〜35分前
後の作用時間をおいて角質繊維を洗浄した後乾燥するこ
とにより行なわれる。ここで染色液の適用は15〜40
℃で行なわれる。
〔発明の効果〕
本発明の染色組成物を用いて角質繊維を染色すれば、顕
色物質とカッf リング物質の組み合せにより黄〜赤〜
青さらに灰色〜黒褐色まで幅広い染色が可能であシ、そ
の色調は高彩度である。特に、レゾルシン系のカップリ
ング物質と組み合せることによシ高彩度の赤系色調が、
またアミノビリシン系のカップリング物質と組み合せる
ことによシ高彩度の黄色が得られる。しかも得られた色
調は良好な耐光性、耐洗浄性及び耐摩擦性を有している
〔実施例〕
次に実施例を挙げて本発明の詳細な説明するが、本発明
はこれによって制限されるものではない。
実施例1 ベース組成: (3b) オレイン酸 オレインはジェタノールアミド         8オ
レイルアルコール エタノール            15ゾロピレング
リコール            10塩化アンモニウ
ム               325チアンモニア
               7水        
               35上記組成からなる
ベース100を中に4゜5.6−1リアミノ−2(1)
1)−ビリミシンチオン0.01モル及び表1に示すカ
ツプリング物質0.01モルを混入した。次いで組成物
の−をアンモニアにて9.5に調整することによシ、本
発明染色組成物を製造した。
本発明染色組成物100tに対し、等重量の6%過酸化
水素水溶液を加えて染色液を調製した。この染色液を白
毛混じシの入毛に塗布し、30℃で30分間放置した。
次いで毛髪を通常のシャンプーで洗浄し、乾燥した。
得られた染色の色調を観察した結果を表1に示す。
以下余白

Claims (1)

  1. 【特許請求の範囲】 1、顕色物質およびカツプリング物質を含有する染色組
    成物において、顕色物質が、次の一般式( I )または
    ( I ′) ▲数式、化学式、表等があります▼( I ) ▲数式、化学式、表等があります▼( I ′) で表わされるトリアミノピリミジン誘導体またはその塩
    であることを特徴とする角質繊維染色組成物。 2、カツプリング物質が、レゾルシン、2−メチルレゾ
    ルシン及び4−クロロレゾルシンからなる群より選ばれ
    る1種もしくは2種以上を含有するものである請求項1
    の角質繊維染色組成物。 3、カツプリング物質が、4−プロピル−2,6−ジア
    ミノピリジン、3,4−ジメチル−2,6−ジアミノピ
    リジンの一方または両方を含有するものである請求項1
    の角質繊維染色組成物。
JP63169571A 1988-07-07 1988-07-07 角質繊維染色組成物 Expired - Fee Related JP2526099B2 (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63169571A JP2526099B2 (ja) 1988-07-07 1988-07-07 角質繊維染色組成物

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63169571A JP2526099B2 (ja) 1988-07-07 1988-07-07 角質繊維染色組成物

Publications (2)

Publication Number Publication Date
JPH0219576A true JPH0219576A (ja) 1990-01-23
JP2526099B2 JP2526099B2 (ja) 1996-08-21

Family

ID=15888943

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63169571A Expired - Fee Related JP2526099B2 (ja) 1988-07-07 1988-07-07 角質繊維染色組成物

Country Status (1)

Country Link
JP (1) JP2526099B2 (ja)

Cited By (272)

* Cited by examiner, † Cited by third party
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US6383231B1 (en) 1998-01-13 2002-05-07 L'oreal Mixture for the oxidation tinting of keratin fibres containing a laccase and tinting method using said mixture
US6402791B1 (en) 1999-01-21 2002-06-11 L'oreal S.A. Cationic di-methylenedioxy-benzenes, their use for oxidation dyeing of keratin fibres
US6455737B1 (en) 1999-01-21 2002-09-24 L'oreal S.A. Cationic a -acylaminophenols, their use as coupler for oxidation dyeing, compositions containing them, and dyeing methods
US6471730B1 (en) 1998-01-13 2002-10-29 L'oreal Dyeing composition containing a laccase and keratinous fiber dyeing methods using same
US6475247B1 (en) 1999-01-21 2002-11-05 L'oreal S.A. Naphthalene cationic coupler for oxidation dyeing of keratin fiber
US6497730B1 (en) 1999-01-21 2002-12-24 L'oreal S.A. Cationic methylenedioxy benzenes, their use for oxidation dyeing of keratin fibers, dyeing compositions and methods
US6530960B1 (en) 1999-10-21 2003-03-11 L'oreal S.A. Composition for oxidation dyeing of keratin fibers and dyeing processes using these compositions
US6537329B1 (en) 1999-01-21 2003-03-25 L'oreal S.A. Cationic 2-sulphonylaminophenols, their use as couplers for oxidation dyeing, compositions containing them and dyeing methods
US6537328B1 (en) 1998-01-13 2003-03-25 L'oreal S.A. Keratinous fibre oxidation dyeing compositions containing a laccase and dyeing method using same
US6544298B1 (en) 1999-01-21 2003-04-08 L'oreal Compositions for oxidation dyeing keratin fibres comprising a cationic coupler novel cationic couplers their use for oxidation dyeing and dyeing methods
US6551359B1 (en) 1998-01-13 2003-04-22 L'oreal S.A. Mixture for the oxidation tinting of keratin fibres containing a laccase and tinting method using said mixture
WO2003041672A1 (de) 2001-11-17 2003-05-22 Henkel Kommanditgesellschaft Auf Aktien Oxidationsfärbemittel auf der basis zweikerniger entwicklerkomponenten
US6572664B2 (en) 2000-02-25 2003-06-03 L'oreal S.A. Indolizine derivatives, compositions comprising at least one coupler chosen from indolizine derivatives and at least one oxidation base, and methods for using same
US6579326B2 (en) 2000-02-25 2003-06-17 L'oreal S.A. Compositions for dyeing keratin fibers, containing cationic indolizine derivatives, and dyeing process
US6599329B1 (en) 1998-01-13 2003-07-29 L'oreal S.A. Keratinous fibre oxidation dyeing composition containing a laccase and dyeing method using same
US6602303B2 (en) 2000-08-11 2003-08-05 L'oreal S.A. Composition for the oxidation dyeing of keratinous fibers comprising at least one oxidation dye and at least one cationic amphiphilic polymer, and dyeing methods
US6605124B1 (en) 1999-01-21 2003-08-12 L'oreal S.A. Cationic couplers and their use for oxidation dyeing
US6626962B1 (en) 1998-01-13 2003-09-30 L'oreal S.A. Mixture for the oxidation tinting of keratin fibers containing a laccase and tinting method using said mixture
US6635091B2 (en) 2000-02-23 2003-10-21 L'oreal S. A. Compositions for the oxidation dyeing of keratinous fibers comprising at least one coupler, and dyeing methods
US6660046B1 (en) 1999-01-19 2003-12-09 L'oreal S.A. Cationic oxidation bases, their use of dyeing keratin fibres, dyeing compositions and dyeing methods
US6673124B2 (en) 1998-03-06 2004-01-06 L'oreal S.A. Oxidation dyeing process and oxidation dye composition for keratin fibers which comprises a cationic amphiphilic polymer
US6673123B2 (en) 1999-12-20 2004-01-06 Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) Solid colorant for keratin fibers
US6695887B2 (en) 1999-12-30 2004-02-24 L'oreal S.A. Compositions for oxidation dyeing keratin fibers comprising at least one fatty alcohol having more than twenty carbon atoms and at least one oxyalkylenated nonionic surfactant with an hlb greater than 5
US6702863B1 (en) 1999-06-22 2004-03-09 Lion Corporation Hairdye composition
US6730133B1 (en) 1999-09-24 2004-05-04 L'oreal S.A. Compositions for oxidation dyeing of at least one keratinous fibre and dying processes using these compositions
US6730789B1 (en) 1999-11-19 2004-05-04 L'oreal S.A. Composition for dyeing keratinous fibers containing 3 amino pyrazolo- [1,5-a] pyridines, dyeing method, novel 3-amino pyrazolo-[1,5-a] pyridines
US6733539B2 (en) 2000-03-30 2004-05-11 L'oreal S.A. Compositions for the oxidation dyeing of keratinous fibers comprising at least one oxidation dye and at least one enzymatic oxidizing agent, and dyeing methods
US6736862B2 (en) 2001-01-10 2004-05-18 Henkel Kommanditgesellschaft Auf Aktien Indole/indoline based hybrid dyes and indole/indoline based hybrid dye intermediate products
US6752839B1 (en) 1999-10-21 2004-06-22 L'oreal Composition for oxidation dyeing of keratin fibres and dyeing processes using these compositions
US6790240B2 (en) 1999-12-20 2004-09-14 Henkel Kommanditgesellschaft Aug Aktien Solid colorant for keratin fibers
US6797012B2 (en) 1999-12-20 2004-09-28 Henkel Kommanditgesellschaft Auf Aktien Solid colorant for keratin fibers
US6800098B1 (en) 1999-12-08 2004-10-05 L'oreal, S.A. Oxidation dye composition for keratinic fibres containing a thickening polymer with an ether plastic skeleton
US6824570B2 (en) 2001-09-26 2004-11-30 L'oreal S.A. Composition for dyeing human keratin fibres, comprising a particular monocationic monoazo dye
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