JP6158041B2 - 毛髪を染色又は脱色するための第2剤組成物 - Google Patents
毛髪を染色又は脱色するための第2剤組成物 Download PDFInfo
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- JP6158041B2 JP6158041B2 JP2013225703A JP2013225703A JP6158041B2 JP 6158041 B2 JP6158041 B2 JP 6158041B2 JP 2013225703 A JP2013225703 A JP 2013225703A JP 2013225703 A JP2013225703 A JP 2013225703A JP 6158041 B2 JP6158041 B2 JP 6158041B2
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- agent
- hair
- dyeing
- alcohol
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
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- A61K8/26—Aluminium; Compounds thereof
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- A61K8/22—Peroxides; Oxygen; Ozone
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
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- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
-
- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
-
- 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
- A61Q5/08—Preparations for bleaching the hair
-
- 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
- A61Q5/10—Preparations for permanently dyeing the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/42—Colour properties
- A61K2800/43—Pigments; Dyes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/49—Solubiliser, Solubilising system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/592—Mixtures of compounds complementing their respective functions
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Description
(1)アルカリ剤を含有する第1剤組成物と混合して使用する、毛髪を染色又は脱色するための第2剤組成物であって、次の成分(A)〜(C):
(A)(a1)少なくとも1種の常温で液状の油剤10〜30重量%、及び、(a2)少なくとも1種の常温で固形状の油剤、ここで、該常温で固形状の油剤は常温で固形状の高級アルコールを含み、(a1)及び(a2)の合計重量(A)と(a2)との重量比(A)/(a2)は3〜8である、
(B)(b1)少なくとも1種のカチオン界面活性剤、及び、(b2)少なくとも1種の非イオン界面活性剤、ここで、該カチオン界面活性剤はアルキル基部分において16〜22個の炭素原子を有する塩化アルキルトリメチルアンモニウムを含み、(b1)及び(b2)の合計重量(B)は0.5〜1.8重量%である、
及び、
(C)酸化剤、0.1〜12重量%
を含有し、(A)と(B)の重量比(A)/(B)は5〜30である、組成物。
(2)(b1)と(b2)の重量比(b1)/(b2)は0.1〜1である、上記(1)に記載の組成物。
(3)高級アルコールは、セチルアルコール、ステアリルアルコール及びセトステアリルアルコールからなる群から選択される少なくとも1種を含む、上記(1)又は(2)に記載の組成物。
(4)非イオン界面活性剤は少なくとも1種のポリオキシエチレンアルキルエーテルを含む、上記(1)〜(3)のいずれかに記載の組成物。
常温で液状の油剤としては、特に限定されないが、例えばエステル油、炭化水素油、シリコーン油、動植物油、常温で液状の高級アルコール及び常温で液状の高級脂肪酸等が挙げられる。エステル油としては、例えば炭素原子数6〜24の脂肪酸、例えば、カプロン酸、カプリル酸、2−エチルヘキサン酸、カプリン酸、ラウリン酸、イソトリデカン酸、ミリスチン酸、パルミチン酸、パルミトレイン酸、ステアリン酸、イソステアリン酸、オレイン酸、エライジン酸、ペトロセリン酸、リノール酸、リノレン酸、エレオステアリン酸、アラキン酸、ガドレイン酸、ベヘン酸、エルカ酸と、アルコール、例えばイソプロピルアルコール、カプロンアルコール、カプリルアルコール、2−エチルヘキシルアルコール、カプリンアルコール、ラウリルアルコール、イソトリデシルアルコール、ミリスチルアルコール、セチルアルコール、パルミトレイルアルコール、ステアリルアルコール、イソステアリルアルコール、オレイルアルコール、エライジルアルコール、ペトロセリニルアルコール、リノリルアルコール、リノレニルアルコール、エレオステアリルアルコール、アラキルアルコール、ガドレイルアルコール、ベヘニルアルコール、エルシルアルコール、ブラシジルアルコールとの、エステル化生成物等が挙げられる。さらに、ジカルボン酸エステル、例えばアジピン酸ジ−n−ブチル、アジピン酸ジ−(2−エチルヘキシル)、コハク酸ジ−(2−エチルヘキシル)及びジイソトリデシルアセラート、並びにジオールエステル、例えばエチレングリコールジオレエート、エチレングリコールジイソトリデカノエート、プロピレングリコールジ−(2−エチルヘキサノエート)、プロピレングリコールジイソステアレート、プロピレングリコールジペラルゴネート、ブタンジオールジイソステアレート、及びネオペンチルグリコールジカプリレート、並びに複合エステル、例えばジアセチルグリセロールモノステアレート等も例として挙げられる。炭化水素油としては、例えば流動パラフィン、ジオクチルシクロヘキサン、α-オレフィンオリゴマー、軽質イソパラフィン、軽質流動イソパラフィン、スクワラン、ポリブテン、流動イソパラフィン等が挙げられる。シリコーン油としては、例えばジメチルポリシロキサン、メチルフェニルポリシロキサン、環状シリコーン、並びにアミノ変性、脂肪酸変性、アルコール変性、ポリエーテル変性、エポキシ変性、フッ素変性及び/又はアルキル変性シリコーン化合物等が挙げられる。動植物油としては、例えばマカデミアナッツ油、ヤシ油、アマランス種子油、桃仁油、アボガド油、オリーブ油、菜種油、ゴマ油、ホホバ油、大豆油、落花生油、メマツヨイグサ油及びチャノキ油等が挙げられる。常温で液状の高級アルコールとしては、例えばヘキシルデカノール、イソステアリルアルコール、オクチルドデカノール、デシルテトラデカノール、オレイルアルコール等が挙げられる。常温で液状の高級脂肪酸としては、例えばイソステアリン酸、オレイン酸及びリノール酸等が挙げられる。本発明の組成物は、これらの常温で液状の油剤を単独で含有してもよいし、2種以上を組み合わせて含有してもよい。
常温で固形状の油剤としては、特に限定されないが、例えば常温で固形状の炭化水素、動物脂、ロウ類、高級脂肪酸、エステル類等が挙げられる。本発明において、「常温で固形状」とは、25℃の温度において固体状又はペースト状であることを意味する。例えば、パラフィンワックス等の炭化水素、ミツロウ等のロウ類を使用してよい。
カチオン界面活性剤としては、例えばエチル硫酸ラノリン脂肪酸アミノプロピルエチルジメチルアンモニウム、塩化ベヘニルトリメチルアンモニウム、塩化オクタデシルアンモニウム、塩化オクチルジヒドロキシエチルメチルアンモニウム、塩化ジアルキル(12〜15)ジメチルアンモニウム、塩化ジアルキル(14〜18)ジメチルアンモニウム、塩化ジココイルジメチルアンモニウム、塩化ジステアリルジメチルアンモニウム、塩化ジセチルジメチルアンモニウム、塩化ジ(ポリオキシエチレン)オレイルメチルアンモニウム、塩化ステアリルジヒドロキシエチルベタインナトリウム、塩化ステアリルジメチルベンジルアンモニウム、塩化ステアリルトリメチルアンモニウム、塩化セチルトリメチルアンモニウム、塩化セチルピリジニウム、塩化ベンザルコニウム、塩化ベンゼトニウム、塩化ポリオキシエチレン(1)ポリオキシプロピレン(25)ジエチルメチルアンモニウム、塩化ミリスチルジメチルベンジルアンモニウム、塩化メチルベンゼトニウム、塩化ラウリルトリメチルアンモニウム、塩化ラウリルピリジニウム、臭化アルキルイソキノリニウム、臭化ステアリルトリメチルアンモニウム、臭化セチルトリメチルアンモニウム、臭化ラウリルトリメチルアンモニウム、ステアリルトリメチルアンモニウムサッカリン、セチルトリメチルアンモニウムサッカリン等が挙げられる。
非イオン界面活性剤としては、特に限定されないが、ポリオキシエチレンアルキルエーテル及びポリオキシエチレンフェニルエーテル等のポリオキシエチレン型非イオン界面活性剤、ポリオキシエチレン脂肪酸エステル、多価アルコールエステル及び高級脂肪酸グリセリンエステル等のエステル型非イオン界面活性剤、アルカノールアミド、アルキルポリグルコシド等が挙げられる。本発明の組成物は、これらの非イオン界面活性剤を単独で含有してもよいし、2種以上を組み合わせて含有してもよい。
本発明の組成物は、毛髪の十分な染色又は脱色を得るために、酸化剤を含有する。酸化剤としては、特に限定されないが、例えば、過酸化水素、過ホウ酸ナトリウム、過ホウ酸カリウム、過炭酸ナトリウム、臭素酸ナトリウムなどが挙げられる。これらの酸化剤を単独で含有してもよいし、2種以上を組み合わせて含有してもよい。これらの中でも、特に過酸化水素が、十分な染色力及び脱色力が得られるため好ましい。
第1剤組成物及び第2剤組成物の剤型は、液状、乳液状、クリ−ム状、ゲル状、ペースト状、フォーム状等の剤型にすることができ、エアゾール形態とすることもできるが、これらの剤型に限定されるものではない。また、第1剤組成物がクリーム状であり、第2剤組成物が液状であるなど、互いに異なる剤型であってもよく、第1剤組成物と第2剤組成物の混合比も問わない。第1剤組成物及び第2剤組成物の剤型は、クリーム状であることが、本発明の組成物の安定性及び染色又は脱色剤組成物の操作性の観点から好ましい。
第1剤のpHは、染色及び脱色力、皮膚刺激性の観点から、8〜12であることが好ましく、9〜11であることがより好ましい。また、第1剤と第2剤を混合して得た染色又は脱色剤組成物のpHは、染色及び脱色力、皮膚刺激性の観点から、8〜12であることが好ましく、8〜10であることがより好ましい。
表2〜4に示す第2剤組成物について、調製直後の組成物の乳化状態を目視にて観察し、次の基準に従い評価した。得られた結果を表2〜4に示す。
◎:非常に良好な乳化状態
〇:上記との比較ではやや粒子が粗いが、良好な乳化状態
△:不均一であり、悪い乳化状態
×:乳化せずクリームにならない
第2剤組成物を、ガラス容器中、50℃で1ヶ月間保存後に、外観の変化を目視にて観察し、次の基準に従い評価した。得られた結果を表2〜4に示す。
◎:変化なし
〇:ほとんど変化なし
△:粘度低下
×:分離
◎:全く液だれせず、毛髪に非常に伸ばしやすい
〇:液だれせず、毛髪に伸ばしやすい
△:液だれしないが、毛髪に伸ばしにくい
×:液だれし、毛髪に伸ばしにくい
◎:髪の弾力及びしなやかさが非常に良好
〇:髪の弾力及びしなやかさが良好
△:髪の弾力及びしなやかさがあまりない
×:髪の弾力及びしなやかさがない
◎:髪のまとまりが非常に良い
〇:髪のまとまりが良い
△:髪のまとまりが悪い
×:髪のまとまりが非常に悪い
◎:非常に滑らかな手触り
〇:滑らかな手触り
△:指通りが悪く、きしみを感じる
×:指通りが非常に悪く、ひっかかる
◎:毛髪が非常によく染色されている
〇:毛髪がよく染色されている
△:毛髪があまり染色されていない
×:毛髪がほとんど染色されていない
◎:染色むらがなく、非常に均一
〇:染色むらがほぼなく、均一
△:染色むらがややある
×:染色むらが多い
Claims (4)
- アルカリ剤を含有する第1剤組成物と混合して使用する、毛髪を染色又は脱色するための第2剤組成物であって、次の成分(A)〜(C):
(A)(a1)少なくとも1種の常温で液状の油剤10〜30重量%、及び、(a2)少なくとも1種の常温で固形状の油剤、ここで、該常温で固形状の油剤は常温で固形状の高級アルコールを含み、(a1)及び(a2)の合計重量(A)と(a2)との重量比(A)/(a2)は3〜8である、
(B)(b1)少なくとも1種のカチオン界面活性剤、及び、(b2)少なくとも1種の非イオン界面活性剤、ここで、該カチオン界面活性剤はアルキル基部分において16〜22個の炭素原子を有する塩化アルキルトリメチルアンモニウムを含み、(b1)及び(b2)の合計重量(B)は0.5〜1.8重量%である、
及び、
(C)酸化剤、0.1〜12重量%
を含有し、(A)と(B)の重量比(A)/(B)は5〜30である、組成物。 - (b1)と(b2)の重量比(b1)/(b2)は0.1〜1である、請求項1に記載の組成物。
- 高級アルコールは、セチルアルコール、ステアリルアルコール及びセトステアリルアルコールからなる群から選択される少なくとも1種を含む、請求項1又は2に記載の組成物。
- 非イオン界面活性剤は少なくとも1種のポリオキシエチレンアルキルエーテルを含む、請求項1〜3のいずれかに記載の組成物。
Priority Applications (4)
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---|---|---|---|
JP2013225703A JP6158041B2 (ja) | 2013-10-30 | 2013-10-30 | 毛髪を染色又は脱色するための第2剤組成物 |
EP14787065.3A EP3062760B1 (en) | 2013-10-30 | 2014-10-06 | Second agent composition for hair dyeing or bleaching |
PCT/JP2014/077121 WO2015064336A1 (en) | 2013-10-30 | 2014-10-06 | Second agent composition for hair dyeing or bleaching |
US15/134,977 US20160256373A1 (en) | 2013-10-30 | 2016-04-21 | Second agent composition for hair dyeing and bleaching |
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JP2013225703A JP6158041B2 (ja) | 2013-10-30 | 2013-10-30 | 毛髪を染色又は脱色するための第2剤組成物 |
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JP6158041B2 true JP6158041B2 (ja) | 2017-07-05 |
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US (1) | US20160256373A1 (ja) |
EP (1) | EP3062760B1 (ja) |
JP (1) | JP6158041B2 (ja) |
WO (1) | WO2015064336A1 (ja) |
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JP6682567B2 (ja) * | 2018-03-30 | 2020-04-15 | ヘンケルジャパン株式会社 | 酸化染毛剤又は毛髪脱色剤の第1剤 |
Family Cites Families (7)
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DE102004017431A1 (de) * | 2004-04-08 | 2005-10-27 | Wella Ag | Verwendung von N-Hydroxyalkyl-O-benzylchitosanen zur Haarbehandlung |
JP5140245B2 (ja) * | 2006-02-14 | 2013-02-06 | 花王株式会社 | 染毛用又は毛髪脱色用第2剤組成物 |
JP2010150180A (ja) * | 2008-12-25 | 2010-07-08 | Henkel Japan Ltd | 酸化染毛剤 |
JP2011020988A (ja) * | 2009-07-16 | 2011-02-03 | Sanei Kagaku Kk | ハロゲン化ラウリルトリメチルアンモニウム含有酸化染毛剤第ii剤、及び酸化染毛剤 |
FR2954093B1 (fr) * | 2009-12-22 | 2012-02-24 | Oreal | Agent de coloration et/ou de decoloration des fibres keratiniques en deux parties ou plus sous forme d'emulsion et de dispersion |
WO2012137877A1 (ja) * | 2011-04-07 | 2012-10-11 | 花王株式会社 | 酸化型染毛剤又は脱色剤組成物 |
JP5794820B2 (ja) * | 2011-04-22 | 2015-10-14 | 花王株式会社 | 酸化型染毛剤又は脱色剤組成物 |
-
2013
- 2013-10-30 JP JP2013225703A patent/JP6158041B2/ja active Active
-
2014
- 2014-10-06 WO PCT/JP2014/077121 patent/WO2015064336A1/en active Application Filing
- 2014-10-06 EP EP14787065.3A patent/EP3062760B1/en active Active
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2016
- 2016-04-21 US US15/134,977 patent/US20160256373A1/en not_active Abandoned
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WO2015064336A1 (en) | 2015-05-07 |
EP3062760A1 (en) | 2016-09-07 |
JP2015086166A (ja) | 2015-05-07 |
US20160256373A1 (en) | 2016-09-08 |
EP3062760B1 (en) | 2017-08-16 |
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