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JP2006111606A - Photocatalyst-containing composition for hair - Google Patents

Photocatalyst-containing composition for hair Download PDF

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JP2006111606A
JP2006111606A JP2004331209A JP2004331209A JP2006111606A JP 2006111606 A JP2006111606 A JP 2006111606A JP 2004331209 A JP2004331209 A JP 2004331209A JP 2004331209 A JP2004331209 A JP 2004331209A JP 2006111606 A JP2006111606 A JP 2006111606A
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hair
oxide
composition
photocatalytic action
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Minoru Kobayashi
穣 小林
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Abstract

<P>PROBLEM TO BE SOLVED: To obtain a photocatalyst-containing composition for hair which contains an effective new material as a substitute for all or a part of an oxidizing agent contained in a cosmetic for hair and a quasi-drug for hair, and hence overcomes conventional defects and is stable for a long time. <P>SOLUTION: This composition provided contains at least one compound having a photocatalytic action as the substitute for all or a part of the conventionally used oxidizing agent. A method for using the composition is also provided. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は、頭髪用品に関する。さらに詳しくは頭髪用化粧品、及び頭髪用医薬部外品に従来配合されていた酸化剤の全て又は、部分に代えて光触媒作用を有する少なくとも1種の半導体を含む頭髪用品に関する。  The present invention relates to hair supplies. More specifically, the present invention relates to a hair product containing at least one semiconductor having a photocatalytic action instead of all or part of the oxidizer conventionally blended in hair cosmetics and quasi drugs for hair.

従来の頭髪用化粧品、及び頭髪用医薬部外品に配合される酸化剤は、図2に示すように、酸化剤自体が分解し、強い酸化作用を有す活性酸素種(O 、OH、H、)を放出するものである。As shown in FIG. 2, the oxidizing agent blended in conventional cosmetics for hair and quasi-pharmaceutical products is decomposed by the oxidizing agent itself and has a strong oxidizing action (O 2 , OH). , H 2 O 2 ,).

しかしながら、以上の技術によれば、保存状態でも分解や変色が起こるので長期間の保存に対応できるpH領域が限定され、活性も抑えられていた。また、配合された他の有効成分を保存期間中徐々に酸化するため配合できる物質に制限があった。さらに、酸化剤自体の分解で酸化作用を有するため、配合量も多量に必要であった。However, according to the above technique, decomposition and discoloration occur even in the storage state, so that the pH range that can be used for long-term storage is limited and the activity is also suppressed. In addition, there is a limit to the substances that can be blended because other blended active ingredients are gradually oxidized during the storage period. Further, since the oxidizing agent itself has an oxidizing action, a large amount of the compound is necessary.

そこで、この発明は、保存期間中は酸化作用を有さず着色や変色のない安定した酸化剤であり、使用時に酸化作用を有し、また少量でも継続的に酸化作用を有する酸化剤を配合した頭髪用化粧品、及び頭髪用医薬部外品を提供することを課題とする。  Therefore, the present invention is a stable oxidizing agent that does not have an oxidizing action during the storage period and has no coloring or discoloration, and has an oxidizing action at the time of use, and also contains an oxidizing agent that has an oxidizing action continuously even in a small amount. It is an object to provide a cosmetic product for hair and a quasi-drug for hair.

以上の課題を解決するために、第一発明は、従来配合されていた酸化剤の全て又は、部分に代えて光触媒作用を有する少なくとも1種の半導体を配合することを特徴とする頭髪用化粧品、及び頭髪用医薬部外品である。本発明において、半導体の配合量は、頭髪用品中、重量として0.001〜20質量%が好ましく、特には0.1〜10質量%である。0.001質量%未満では本願発明効果が十分に発揮され難く、一方、20質量%を超えて配合してもさほど大きな効果の向上は認められず、また製剤化が難しくなるので好ましくない。  In order to solve the above-mentioned problems, the first invention is a cosmetic for hair characterized by blending at least one semiconductor having a photocatalytic action in place of all or part of the oxidizer conventionally blended, And quasi-drugs for hair. In the present invention, the blending amount of the semiconductor is preferably 0.001 to 20% by mass, particularly 0.1 to 10% by mass in the hair product. If it is less than 0.001% by mass, the effect of the present invention is not sufficiently exhibited. On the other hand, even if it exceeds 20% by mass, no significant improvement in the effect is observed, and it becomes difficult to formulate.

また、第二発明は、光触媒作用を有する少なくとも1種の半導体を配合し、この製品の使用時に蛍光灯、ブラックライト及び、超高圧水銀灯の少なくとも1種を使用することを特徴とする使用方法である。  The second invention is a method of use characterized in that at least one semiconductor having a photocatalytic action is blended, and at least one of a fluorescent lamp, a black light, and an ultrahigh pressure mercury lamp is used when the product is used. is there.

第一発明、または第二発明によれば、酸化剤として光触媒作用を有する半導体を使用するため半導体自体は分解されない。特に酸化チタンは水中でも溶出せず、図1に示すように、光の照射を受けて触媒上にO 、OH、H等の活性酸素種を生成し継続的に酸化作用を有し、少量の配合量でも継続した酸化反応が可能である。これらは光半導体の価電子帯、伝導帯内に生成した正孔・電子が水酸基、水、吸着酸素などと結合して生じる。また、保存期間中は遮光することで酸化作用を有さないで製品の酸化による劣化がなく長期間の保存が可能である。According to the first invention or the second invention, since a semiconductor having a photocatalytic action is used as an oxidizing agent, the semiconductor itself is not decomposed. In particular, titanium oxide does not elute in water, and as shown in FIG. 1, it generates active oxygen species such as O 2 , OH , and H 2 O 2 on the catalyst upon irradiation with light and continuously oxidizes it. The oxidation reaction can be continued even with a small amount. These occur when holes and electrons generated in the valence band and conduction band of an optical semiconductor are combined with hydroxyl, water, adsorbed oxygen, and the like. In addition, during the storage period, the product is shielded from light so that it does not have an oxidizing action and the product is not deteriorated due to oxidation and can be stored for a long period of time.

次に、実施例によって本発明をさらに詳細に説明するが、本発明の技術的範囲はこれら実施例によってなんら限定されるものではない。なお、配合量は、特記しない限り質量%で示す。  EXAMPLES Next, although an Example demonstrates this invention further in detail, the technical scope of this invention is not limited at all by these Examples. In addition, unless otherwise indicated, the blending amount is indicated by mass%.

(比較例1〜3、実施例1〜12)
従来使用されていた酸化剤として臭素酸ナトリウム、臭素酸カリウム、過酸化水素を用いて経時安定性をみた。具体的には、表1に記載する各成分を混合加熱して被験組成物(比較例1〜3、実施例1〜12)を調整し、下記の評価方法により経時安定性を評価した。この結果を併せて比較例1〜3を表1に、実施例1〜12を表2に示す。
(Comparative Examples 1-3, Examples 1-12)
Stability over time was observed using sodium bromate, potassium bromate, and hydrogen peroxide as oxidants conventionally used. Specifically, each component described in Table 1 was mixed and heated to prepare test compositions (Comparative Examples 1 to 3, Examples 1 to 12), and the temporal stability was evaluated by the following evaluation method. Together with these results, Comparative Examples 1 to 3 are shown in Table 1, and Examples 1 to 12 are shown in Table 2.

(概観による評価方法)
被験組成物の調整時と45℃の恒温層放置後の色調等の変化による評価。
◎:色調等の変化がまったく見られない。
○:若干の変色、着色がみられる。
●:明らかに変色、着色が確認される。
×:ガスの発生が確認される。
(Evaluation method by overview)
Evaluation based on changes in color tone and the like after adjustment of the test composition and after standing at a constant temperature layer of 45 ° C.
A: No change in color tone or the like is observed.
○: Some discoloration and coloring are observed.
●: Discoloration and coloring are clearly confirmed.
X: Generation of gas is confirmed.

Figure 2006111606
Figure 2006111606

表1の結果以外に臭素酸ナトリウム、臭素酸カリウムは、調整時のpHを7.0付近又は、それ以上に調整すると概観の変化なく長期保存が可能であることがわかった。  In addition to the results shown in Table 1, it was found that sodium bromate and potassium bromate can be stored for a long period of time without change in appearance when the pH during adjustment is adjusted to around 7.0 or higher.

Figure 2006111606
Figure 2006111606

これらの結果から、光触媒作用を有す半導体は分解や変色のない安定した酸化剤であることが認められた。以下に示す実施例においても、同様の評価方法を行った。  From these results, it was confirmed that a semiconductor having a photocatalytic action is a stable oxidizing agent without decomposition or discoloration. The same evaluation method was performed also in the Example shown below.

<実施例13>ヘアトニック
原料名 重量%

ポリオキシエチレン硬化ヒマシ油 1.0
トウガラシチンキ 0.1
酢酸トコフェロール 0.05
95%未変性エタノール 50.0

パラオキシ安息香酸エステル 0.3
95%未変性アルコール 5.0
酸化チタン 0.1
精製水 適量
Aに属する成分を加熱溶解する。別に、Bに属する成分を分散する。AにBを添加して、撹拌、混合後、冷却してヘアトニックを製造した。
<Example 13> Hair tonic raw material weight%
A
Polyoxyethylene hydrogenated castor oil 1.0
Pepper tincture 0.1
Tocopherol acetate 0.05
95% native ethanol 50.0
B
P-Hydroxybenzoate ester 0.3
95% unmodified alcohol 5.0
Titanium oxide 0.1
Purified water Heat-dissolve ingredients belonging to appropriate amount A. Separately, the component belonging to B is dispersed. B was added to A, stirred, mixed and then cooled to produce a hair tonic.

<実施例14>ヘアシャンプー
原料名 重量%

エデト酸二ナトリウム 0.1
パラオキシ安息香酸エステル 0.3
1,3−ブチレングリコール 10.0
クエン酸 0.5
精製水 適量

ヤシ油脂肪酸メチルタウリンナトリウム 20.0
ポリオキシエチレンラウリルエーテル硫酸ナトリウム 20.0
ラウリル酸アミドプロピルベタイン 10.0
ジステアリン酸エチレングリコール 2.0
ポリオキシエチレンラウリルエーテル 1.0
酸化チタン 1.0
Aに属する成分を加熱溶解する。別に、Bに属する成分を加熱溶解する。AにBを添加して、撹拌、乳化後、冷却してヘアシャンプーを製造した。
<Example 14> Hair shampoo raw material name% by weight
A
Edetate disodium 0.1
P-Hydroxybenzoate ester 0.3
1,3-butylene glycol 10.0
Citric acid 0.5
Purified water appropriate amount B
Palm oil fatty acid sodium methyltaurine 20.0
Sodium polyoxyethylene lauryl ether sulfate 20.0
Amidopropyl betaine laurate 10.0
Ethylene glycol distearate 2.0
Polyoxyethylene lauryl ether 1.0
Titanium oxide 1.0
The components belonging to A are dissolved by heating. Separately, the component belonging to B is dissolved by heating. B was added to A, stirred and emulsified, and then cooled to produce a hair shampoo.

<実施例15>ヘアリンス
原料名 重量%

セチルアルコール 5.0
パルミチン酸イソプロピル 5.0
ジメチコン 2.0
ホホバ油 2.0
塩化ステアリルトリメチルアンモニウム 2.0
ポリオキシエチレンオレイルエーテル 1.0
酸化チタン 0.3

グリセリン 10.0
カチオン化セルロース 0.6
パラオキシ安息香酸エステル 0.6
精製水 適量
Aに属する成分を加熱溶解する。別に、Bに属する成分を加熱溶解する。AにBを添加して、撹拌、乳化後、冷却してヘアリンスを製造した。
<Example 15> Hair rinse raw material weight%
A
Cetyl alcohol 5.0
Isopropyl palmitate 5.0
Dimethicone 2.0
Jojoba oil 2.0
Stearyltrimethylammonium chloride 2.0
Polyoxyethylene oleyl ether 1.0
Titanium oxide 0.3
B
Glycerin 10.0
Cationized cellulose 0.6
P-Hydroxybenzoate ester 0.6
Purified water Heat-dissolve ingredients belonging to appropriate amount A Separately, the component belonging to B is dissolved by heating. B was added to A, stirred and emulsified, and then cooled to produce a hair rinse.

<実施例16>パーマネントウェーブ用第2剤
原料名 重量%
過酸化水素 1.5
酸化チタン 0.3
グリセリン 10.0
ポリオキシエチレンラウリルエーテル 1.0
パラオキシ安息香酸エステル 0.6
精製水 適量
上記成分を混合、撹拌してパーマネントウェーブ用第2剤を製造した。
<Example 16> Name of second agent raw material for permanent wave Weight%
Hydrogen peroxide 1.5
Titanium oxide 0.3
Glycerin 10.0
Polyoxyethylene lauryl ether 1.0
P-Hydroxybenzoate ester 0.6
Purified water An appropriate amount of the above ingredients were mixed and stirred to produce a second agent for permanent wave.

<実施例17>毛髪脱色剤 第二剤
原料名 重量%

セタノール 5.0
ポリオキシエチレンステアリルエーテル 2.0
塩化ステアリルトリメチルアンモニウム 0.6

スズ酸ナトリウム 0.05
リン酸 0.3
精製水 適量

過酸化水素 5.0
酸化チタン 1.0
Aに属する成分を加熱溶解する。別に、Bに属する成分を加熱溶解する。AにBを添加して、撹拌、乳化後、冷却し、Cに属する成分を添加、撹拌し毛髪脱色剤第二剤を製造した。
<Example 17> Hair bleaching agent Second agent raw material name Weight%
A
Cetanol 5.0
Polyoxyethylene stearyl ether 2.0
Stearyltrimethylammonium chloride 0.6
B
Sodium stannate 0.05
Phosphoric acid 0.3
Purified water appropriate amount C
Hydrogen peroxide 5.0
Titanium oxide 1.0
The components belonging to A are dissolved by heating. Separately, the component belonging to B is dissolved by heating. B was added to A, stirred and emulsified, cooled, the components belonging to C were added and stirred, and a hair bleaching agent second agent was produced.

<実施例18>染毛剤 第二剤
原料名 重量%

セタノール 3.0
ポリオキシエチレンステアリルエーテル 2.0
流動パラフィン 10.0

エデト酸二ナトリウム 0.1
クエン酸 0.2
精製水 適量

過酸化水素 5.0
酸化チタン 1.0
Aに属する成分を加熱溶解する。別に、Bに属する成分を加熱溶解する。AにBを添加して、撹拌、乳化後、冷却し、Cに属する成分を添加、撹拌し染毛剤第二剤を製造した。
<Example 18> Hair dye Second agent raw material name Weight%
A
Cetanol 3.0
Polyoxyethylene stearyl ether 2.0
Liquid paraffin 10.0
B
Edetate disodium 0.1
Citric acid 0.2
Purified water appropriate amount C
Hydrogen peroxide 5.0
Titanium oxide 1.0
The components belonging to A are dissolved by heating. Separately, the component belonging to B is dissolved by heating. B was added to A, and after stirring and emulsification, the mixture was cooled, the components belonging to C were added and stirred, and a hair dye second agent was produced.

<実施例19>ヘアワックス
原料名 重量%
キャンデリラロウ 5.0
マイクロクリスタリンワックス 1.0
酸化チタン 2.0
ミリスチン酸イソプロピル 20.0
酢酸ビニル・クロトン酸共重合体 0.05
ステアリン酸 5.0
水酸化ナトリウム 0.3
フェノキシエタノール 0.6
クエン酸 0.5
精製水 適量
上記成分を混合、過熱、撹拌してヘアワックスを製造した。
<Example 19> Name of raw material for hair wax Weight%
Candelilla Row 5.0
Microcrystalline wax 1.0
Titanium oxide 2.0
Isopropyl myristate 20.0
Vinyl acetate / crotonic acid copolymer 0.05
Stearic acid 5.0
Sodium hydroxide 0.3
Phenoxyethanol 0.6
Citric acid 0.5
Purified water An appropriate amount of the above ingredients were mixed, heated and stirred to produce a hair wax.

<実施例20>ヘアクリーム
原料名 重量%

モノステアリン酸ポリオキシエチレンソルビタン 2.0
ポリオキシエチレンセチルエーテル 1.0
モノステアリン酸グリセリル 0.5
ステアリン酸 2.0
ベヘニルアルコール 1.0
流動パラフィン 20.0
パラオキシ安息香酸エステル 0.6
酸化チタン 0.5

1.3−ブチレングリコール 2.0
精製水 適量
Aに属する成分を加熱溶解する。別に、Bに属する成分を加熱溶解する。AにBを添加して、撹拌、乳化後、冷却しヘアクリームを製造した。
<Example 20> Name of hair cream raw material Weight%
A
Polyoxyethylene sorbitan monostearate 2.0
Polyoxyethylene cetyl ether 1.0
Glyceryl monostearate 0.5
Stearic acid 2.0
Behenyl alcohol 1.0
Liquid paraffin 20.0
P-Hydroxybenzoate ester 0.6
Titanium oxide 0.5
B
1.3-Butylene glycol 2.0
Purified water Heat-dissolve ingredients belonging to appropriate amount A. Separately, the component belonging to B is dissolved by heating. B was added to A, stirred and emulsified, and then cooled to produce a hair cream.

実施例13〜20の頭髪用品においても、光触媒作用を有す半導体は分解や変色のない安定した酸化剤であることが認められた。  Also in the hair products of Examples 13 to 20, it was confirmed that the semiconductor having a photocatalytic action was a stable oxidizing agent without decomposition or discoloration.

この発明の酸化剤である光触媒による活性酸素種の生成過程である。This is a process of generating active oxygen species by the photocatalyst which is the oxidizing agent of the present invention. 従来技術の酸化剤による活性酸素種の生成過程である。This is a process of generating reactive oxygen species by a conventional oxidant.

符号の説明Explanation of symbols

1 水
2 酸化剤(TiO等)
3 光源(日光、ブラックライト、蛍光灯、超高圧水銀灯、水銀灯等)
4 光触媒に光が照射され電子と正孔が生成される。
5 電子が溶存酸素を活性化し活性酸素にする。
6 触媒表面の正孔で水がヒドロキシイオンと水素イオンに分解される。
7 水素イオンと活性酸素が化学結合する。
8 さらに、過酸化水素が生成される。
9 臭素酸カリウムによる活性酸素の生成。
10 臭素酸ナトリウムによる活性酸素の生成。
1 Water 2 Oxidizing agent (TiO 2 etc.)
3 Light source (sunlight, black light, fluorescent lamp, ultra-high pressure mercury lamp, mercury lamp, etc.)
4 Light is irradiated to the photocatalyst to generate electrons and holes.
5 Electrons activate dissolved oxygen to make it active oxygen.
6 Water is decomposed into hydroxy ions and hydrogen ions by holes on the catalyst surface.
7 Hydrogen ions and active oxygen are chemically bonded.
8 Furthermore, hydrogen peroxide is produced.
9 Production of active oxygen by potassium bromate.
10 Production of active oxygen by sodium bromate.

Claims (5)

光触媒作用を持つ半導体を頭髪用化粧品及び頭髪用医薬部外品に配合することを特徴とする組成物。A composition comprising a semiconductor having a photocatalytic action in hair cosmetics and quasi-pharmaceutical products for hair. 光触媒作用を持つ半導体が1.5〜5.0eVの荷電子帯と伝導体の間のバンドギャップエネルギーを有し、荷電子帯が水素電極電位を基準として1.2Vよりもプラス側にも存在することを特徴とする請求項1記載の組成物。A semiconductor with a photocatalytic action has a band gap energy between a valence band of 1.5 to 5.0 eV and a conductor, and the valence band is also present on the positive side of 1.2 V with respect to the hydrogen electrode potential. The composition according to claim 1. 光触媒作用を持つ半導体が酸化チタン(TiO)、酸化亜鉛(ZnO)、酸化鉄(Fe)、酸化ニオブ(Nb)、酸化タングステン(WO)、酸化スズ(SnO)、チタン酸ストロンチウム(SrTiO)、セレン化カドミウム(CdSe)、タンタル酸カリウム(KTaO)、硫化カドミウム(CdS)、酸化ジルコニウム(ZrO)、ガリウムリン(GaP)、のいずれか少なくとも1種であるか、またはそれを含む化合物であることを特徴とする請求項1または2に記載の組成物。Semiconductors with photocatalytic action are titanium oxide (TiO 2 ), zinc oxide (ZnO), iron oxide (Fe 2 O 3 ), niobium oxide (Nb 2 O 5 ), tungsten oxide (WO 3 ), tin oxide (SnO 2 ). , Strontium titanate (SrTiO 3 ), cadmium selenide (CdSe), potassium tantalate (KTaO 3 ), cadmium sulfide (CdS), zirconium oxide (ZrO 2 ), gallium phosphide (GaP) 3. A composition according to claim 1 or 2, characterized in that it is or is a compound comprising it. さらに過酸化水素(H)、臭素酸ナトリウム(NaBrO)、臭素酸カリウム(KBrO)、白金(Pt)のいずれか少なくとも1種を含有する請求項1乃至3のいずれかに記載の組成物。Further hydrogen peroxide (H 2 O 2), sodium bromate (NaBrO 3), potassium bromate (KBrO 3), according to any one of claims 1 to 3 containing at least one one of platinum (Pt) Composition. 請求項1乃至4のいずれかに記載の組成物の使用時に蛍光灯、ブラックライト、水銀灯及び、超高圧水銀灯の少なくとも1種を使用することを特徴とする使用方法。A method of use, wherein at least one of a fluorescent lamp, a black light, a mercury lamp, and an ultra-high pressure mercury lamp is used when the composition according to any one of claims 1 to 4 is used.
JP2004331209A 2004-10-18 2004-10-18 Photocatalyst-containing composition for hair Pending JP2006111606A (en)

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Cited By (4)

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Publication number Priority date Publication date Assignee Title
JP2012097047A (en) * 2010-11-04 2012-05-24 Nof Corp Hair cosmetic
WO2013190484A1 (en) * 2012-06-20 2013-12-27 Koninklijke Philips N.V. A comb
KR101860484B1 (en) 2010-09-06 2018-05-23 (주)아모레퍼시픽 A Cosmetic Composition for Producing an Oxygen
FR3116434A1 (en) * 2020-11-24 2022-05-27 L'oreal Use of a particular metal oxide for the photoconversion of organic compounds on keratin materials

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JPS50107147A (en) * 1974-02-12 1975-08-23
JPS5718606A (en) * 1980-07-09 1982-01-30 Hoou Kk Powdered oxidative hair-dyeing composition
JPH07277935A (en) * 1994-03-14 1995-10-24 Hans Schwarzkopf Gmbh Aqueous dyeing agent for keratin fiber
JP2000212012A (en) * 1999-01-14 2000-08-02 Ekuseru Light Kk Composition for animal body hair
JP2000256108A (en) * 1999-03-04 2000-09-19 Lion Corp Composition containing preservative and cinnamic acid derivative
JP2002241250A (en) * 2001-02-02 2002-08-28 L'oreal Sa Fine powder composition for bleaching human keratin fibers
JP2004131454A (en) * 2002-10-15 2004-04-30 Shiseido Co Ltd Perming first agent
WO2004075680A2 (en) * 2003-01-27 2004-09-10 L'oréal Use of a photocatalyst for the treatment of oily hair
JP2005082708A (en) * 2003-09-09 2005-03-31 Soushin:Kk Detergent
JP2008508262A (en) * 2004-07-30 2008-03-21 コリア リサーチ インスティテュートオフ゛ ケミカル テクノロシ゛ー Self-formation permanent agent, rod removal and band removal type permanent method

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JPS50107147A (en) * 1974-02-12 1975-08-23
JPS5718606A (en) * 1980-07-09 1982-01-30 Hoou Kk Powdered oxidative hair-dyeing composition
JPH07277935A (en) * 1994-03-14 1995-10-24 Hans Schwarzkopf Gmbh Aqueous dyeing agent for keratin fiber
JP2000212012A (en) * 1999-01-14 2000-08-02 Ekuseru Light Kk Composition for animal body hair
JP2000256108A (en) * 1999-03-04 2000-09-19 Lion Corp Composition containing preservative and cinnamic acid derivative
JP2002241250A (en) * 2001-02-02 2002-08-28 L'oreal Sa Fine powder composition for bleaching human keratin fibers
JP2004131454A (en) * 2002-10-15 2004-04-30 Shiseido Co Ltd Perming first agent
WO2004075680A2 (en) * 2003-01-27 2004-09-10 L'oréal Use of a photocatalyst for the treatment of oily hair
JP2005082708A (en) * 2003-09-09 2005-03-31 Soushin:Kk Detergent
JP2008508262A (en) * 2004-07-30 2008-03-21 コリア リサーチ インスティテュートオフ゛ ケミカル テクノロシ゛ー Self-formation permanent agent, rod removal and band removal type permanent method

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101860484B1 (en) 2010-09-06 2018-05-23 (주)아모레퍼시픽 A Cosmetic Composition for Producing an Oxygen
JP2012097047A (en) * 2010-11-04 2012-05-24 Nof Corp Hair cosmetic
WO2013190484A1 (en) * 2012-06-20 2013-12-27 Koninklijke Philips N.V. A comb
FR3116434A1 (en) * 2020-11-24 2022-05-27 L'oreal Use of a particular metal oxide for the photoconversion of organic compounds on keratin materials
WO2022112053A1 (en) * 2020-11-24 2022-06-02 L'oreal Use of a particular metal oxide for the photoconversion of organic compounds on keratin materials
CN116583256A (en) * 2020-11-24 2023-08-11 欧莱雅 Use of specific metal oxides for photoconversion of organic compounds on keratin materials
JP2023549367A (en) * 2020-11-24 2023-11-24 ロレアル Use of certain metal oxides for phototransformation of organic compounds on keratin materials
JP7629526B2 (en) 2020-11-24 2025-02-13 ロレアル Use of certain metal oxides for the photoconversion of organic compounds on keratinous materials.

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