JPH0578229A - Hair bleaching agent - Google Patents

Hair bleaching agent

Info

Publication number
JPH0578229A
JPH0578229A JP23974391A JP23974391A JPH0578229A JP H0578229 A JPH0578229 A JP H0578229A JP 23974391 A JP23974391 A JP 23974391A JP 23974391 A JP23974391 A JP 23974391A JP H0578229 A JPH0578229 A JP H0578229A
Authority
JP
Japan
Prior art keywords
hair
acid
agent
bleaching
ascorbic acid
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
JP23974391A
Other languages
Japanese (ja)
Other versions
JP3122182B2 (en
Inventor
Katsuaki Suzuki
克明 鈴木
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.)
Hoyu Co Ltd
Original Assignee
Hoyu Co Ltd
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 Hoyu Co Ltd filed Critical Hoyu Co Ltd
Priority to JP03239743A priority Critical patent/JP3122182B2/en
Publication of JPH0578229A publication Critical patent/JPH0578229A/en
Application granted granted Critical
Publication of JP3122182B2 publication Critical patent/JP3122182B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To provide a hair bleaching agent capable of moderately bleaching hair without using oxidizing agent, free from the damage on hair and stimulation to scalp and giving extremely excellent bleached hair free from the change of the brightness of hair after bleaching. CONSTITUTION:The objective new-type hair bleaching agent free from oxidizing agent and having the above effects can be produced by compounding (A) ascorbic acid or its derivative, preferably ascorbic acid or a higher fatty acid ester of ascorbic acid such as ascorbyl stearate, ascorbyl palmitate and ascorbyl dipalmitate as an essential component in an amount of usually 0.1-30wt.% (preferably 1-25wt.%) and preferably further (B) an organic acid such as citric acid, tartaric acid, lactic acid, succinic acid, malic acid and acetic acid in an amount of e.g. 0.01-5wt.% and adjusting the pH of the hair bleaching agent to usually 1.5-8, preferably 2-7.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は毛髪脱色剤に関するもの
であり、詳しくは、酸化剤を使用しない新しいタイプの
毛髪脱色剤に関するものである。
FIELD OF THE INVENTION The present invention relates to a hair bleaching agent, and more particularly to a new type of hair bleaching agent which does not use an oxidizing agent.

【0002】[0002]

【従来技術】従来、毛髪脱色剤としては種々のタイプの
ものが市販されており、通常、下記の3剤式〜1剤式の
ものが知られている。 ・3剤式…第1剤(液体)アルカリ剤、界面活性剤 第2剤(液体)酸化剤 活性化剤(粉末)過酸化物 使用時に第1剤に活性化剤を添加し、次いで第2剤と混
合する。
2. Description of the Related Art Conventionally, various types of hair depigmenting agents are commercially available, and the following three-part to one-part types are generally known.・ Three-agent type ... First agent (liquid) alkali agent, surfactant Second agent (liquid) oxidizing agent Activator (powder) peroxide Add activator to the first agent at the time of use, then second agent Mix with the agent.

【0003】・2剤式…第1剤(液体)アルカリ剤、界
面活性剤,過酸化物 第2剤(液体)酸化剤 使用時に第1剤と第2剤を混合する。 ・2剤式…第1剤(粉末)アルカリ剤、増粘剤、及び/
又は過酸化物 第2剤(液体)酸化剤 使用時、第2剤に第1剤を添加する。
Two-agent type ... First agent (liquid) alkali agent, surfactant, peroxide Second agent (liquid) oxidizer The first agent and the second agent are mixed when used.・ Two-agent type ... First agent (powder) alkali agent, thickener, and / or
Alternatively, when using a peroxide second agent (liquid) oxidizing agent, the first agent is added to the second agent.

【0004】・1剤式…(粉末)酸化剤、アルカリ剤、
増粘剤、過酸化物 使用時、水に溶解させる。 ・1剤式…(液体)酸化剤 しかしながら、これらの毛髪脱色剤は、いずれも、酸化
剤を含有し発生期の酸素によりメラニン顆粒を酸化分解
することにより、黒髪を褐色〜黄色に脱色するものであ
るが、メラニン顆粒は毛髪の皮質乃至髄質中に存在して
いるため、脱色過程において毛髪ケラチン自体も酸化を
受けると言う問題点がある。このことに関しては、例え
ば、J.SOC.Cosmet.Chem.Vol.1
7,1966年,P687(H.Zahn)には、この
ケラチンの酸化は先ずシスチン結合において起ると報告
されており、また、同誌Vol.20,1969年,P
555(C.Robbins等)には、他のアミノ酸残
基も若干酸化を受けると報告されている。
1-agent type (powder) oxidizing agent, alkaline agent,
Thickener, peroxide When used, dissolve in water.・ One-agent type (liquid) oxidizing agent However, all of these hair decolorizing agents contain an oxidizing agent and decolorize black hair to brown to yellow by oxidatively decomposing melanin granules by nascent oxygen. However, since the melanin granules are present in the cortex or medulla of the hair, there is a problem that the hair keratin itself is also oxidized during the decolorization process. Regarding this, for example, J. SOC. Cosmet. Chem. Vol. 1
7, 1966, P687 (H. Zahn), it is reported that the oxidation of keratin first occurs at the cystine bond, and also in Vol. 20, 1969, P
555 (C. Robbins et al.) Reported that other amino acid residues were also slightly oxidized.

【0005】このように発生期の酸素を利用する毛髪の
脱色においては、メラニン顆粒の酸化分解のみならず、
毛髪ケラチンに対しても重大な損傷を与える結果とな
り、そのため、脱色処理により毛髪はパサツキ、ゴワツ
キ、毛切れなどが起り、艶のない毛髪となる。また、脱
色後においてもメラニン色素が徐々に流出し、毛髪の色
が次第に明るくなると言う欠点もある。
As described above, in the decolorization of hair utilizing nascent oxygen, not only oxidative decomposition of melanin granules but also
As a result, serious damage is also caused to the hair keratin, and therefore, the decolorizing treatment causes the hair to become dull, dull, and broken, resulting in dull hair. Further, there is also a drawback that the melanin pigment gradually flows out even after bleaching, and the color of hair gradually becomes brighter.

【0006】[0006]

【発明が解決しようとする課題】本発明は上記実情に鑑
み、酸化剤を使用することなく、毛髪の脱色を行なうこ
とができ、しかも、毛髪に対する損傷及び頭皮への刺激
のない毛髪脱色剤を提供することを目的とする。
In view of the above situation, the present invention provides a hair bleaching agent that can decolorize hair without using an oxidizing agent, and that does not damage hair or irritate the scalp. The purpose is to provide.

【0007】[0007]

【課題を解決するための手段】本発明者は上記の目的を
達成すべく鋭意検討を重ねた結果、アスコルビン酸又は
その誘導体に毛髪の脱色作用があり、また、これを毛髪
に施用した場合、毛髪の損傷がなく、艶のあるしっとり
とした仕上りとなる上、脱色後も毛髪の色が明るく変化
することもないことを見い出し本発明を完成した。
Means for Solving the Problems As a result of intensive studies to achieve the above object, the present inventor has found that ascorbic acid or a derivative thereof has a decolorizing effect on hair, and when it is applied to hair, The present invention has been completed by finding that the hair is not damaged, has a glossy and moist finish, and that the color of the hair does not change brightly even after decolorization.

【0008】以下、本発明の構成につき詳細に説明す
る。本発明において対象となるアスコルビン酸又はその
誘導体としては、通常、アスコルビン酸、アスコルビン
酸ナトリウムなどのアスコルビン酸塩、ステアリン酸ア
スコルビル、パルミチン酸アスコルビル、ジパルミチン
酸アスコルビルなどのアスコルビン酸高級脂肪酸エステ
ル、アスコルビン酸リン酸エステルマグネシウムなどの
アスコルビン酸エステル、アスコルビン酸硫酸エステル
ニナトリウム、アスコルビン酸酢酸エステル、アスコル
ビン酸安息香酸エステル、エリソルビン酸などが挙げら
れる。これらの化合物の中で毛髪の脱色作用から最も好
ましいものは、アスコルビン酸及びアスコルビン酸高級
脂肪酸エステルである。
The structure of the present invention will be described in detail below. The target ascorbic acid or a derivative thereof in the present invention, ascorbic acid, ascorbate salts such as sodium ascorbate, ascorbyl stearate, ascorbyl palmitate, ascorbyl higher fatty acid ester such as ascorbyl dipalmitate, ascorbic acid. Examples thereof include ascorbic acid ester such as magnesium phosphate, ascorbic acid sulfate disodium salt, ascorbic acid acetic acid ester, ascorbic acid benzoic acid ester, and erythorbic acid. Among these compounds, the most preferable ones from the viewpoint of hair decolorizing action are ascorbic acid and ascorbic acid higher fatty acid ester.

【0009】アスコルビン酸又はその誘導体の毛髪脱色
剤への配合量は、通常、0.1〜30重量%、好ましく
は1〜25重量%、更に好ましくは2〜20重量%であ
る。この配合量があまり少な過ぎると良好な毛髪の脱色
効果を得ることができず、逆にあまり多過ぎても効果に
変りはなく経済的ではない。
The amount of ascorbic acid or its derivative incorporated into the hair decolorizing agent is usually 0.1 to 30% by weight, preferably 1 to 25% by weight, more preferably 2 to 20% by weight. If the blending amount is too small, a good hair decolorizing effect cannot be obtained, and conversely, if the blending amount is too large, the effect does not change and it is not economical.

【0010】本発明では上述のアスコルビン酸又はその
誘導体とともに、有機酸を併用すると、更に優れた毛髪
脱色効果を得ることができるので望ましい。この場合の
有機酸としては、通常、クエン酸、酒石酸、乳酸、コハ
ク酸、リンゴ酸、酢酸などが挙げられる。。また、その
配合量は、例えば、0.01〜5重量%である。この有
機酸の配合により毛髪脱色剤のpHは通常、1.5〜
8、好ましくは2〜7に調整される。
In the present invention, it is desirable to use an organic acid in combination with the above-mentioned ascorbic acid or its derivative because a more excellent hair decolorizing effect can be obtained. In this case, the organic acid usually includes citric acid, tartaric acid, lactic acid, succinic acid, malic acid, acetic acid and the like. .. The blending amount is, for example, 0.01 to 5% by weight. With the addition of this organic acid, the pH of the hair decolorizing agent is usually 1.5-
It is adjusted to 8, preferably 2 to 7.

【0011】更に、本発明の毛髪脱色剤には種々の公知
の添加剤を配合することができる。これらの添加剤とし
ては、例えば、界面活性剤、増粘剤、ポリペプチドなど
が挙げられる。界面活性剤としては、通常、カチオン性
界面活性剤、アニオン性界面活性剤、非イオン性界面活
性剤、両性界面活性剤が挙げられるが、なかでも、アス
コルビン酸又はその誘導体の毛髪への浸透を良好に促進
させるためには、非イオン性界面活性剤が好ましい。増
粘剤としては、デンプン質、海藻類、アルギン酸ナトリ
ウム、メチルセルロース、ヒドロキシエチルセルロー
ズ、カルボキシメチルセルローズ、ポリビニルアルコー
ル、ポリビニルピロリドン、ポリアクリル酸ソーダ、グ
アーガム、第四級窒素含有セルロースエーテル、キサン
タンガム等が挙げられる。また、ポリペプタイドとして
は、コラーゲン、ケラチン、エラスチン、フィブロイ
ン、コンキオリン、大豆蛋白、カゼイン等の蛋白質を
酸、アルカリ、酵素等をより加水分解した加水分解物、
及びこれらを4級化したカチオン変性蛋白質が挙げられ
る。その他、プロピレングリコールなどのグリコール
類、エタノール、プロパノールなどのアルコール類、水
溶性シリコーン等も必要に応じて配合することができ
る。
Further, various known additives can be added to the hair bleaching agent of the present invention. Examples of these additives include surfactants, thickeners, polypeptides and the like. As the surfactant, there are usually mentioned cationic surfactants, anionic surfactants, nonionic surfactants and amphoteric surfactants. Among them, the penetration of ascorbic acid or its derivatives into hair is recommended. Nonionic surfactants are preferred for good promotion. Examples of the thickener include starch, seaweed, sodium alginate, methyl cellulose, hydroxyethyl cellulose, carboxymethyl cellulose, polyvinyl alcohol, polyvinylpyrrolidone, sodium polyacrylate, guar gum, quaternary nitrogen-containing cellulose ether, xanthan gum and the like. Be done. Further, as the polypeptide, collagen, keratin, elastin, fibroin, conchiolin, soybean protein, acid such as soybean protein, casein, a hydrolyzate obtained by further hydrolyzing an enzyme,
And cation-denatured proteins obtained by quaternizing these. In addition, glycols such as propylene glycol, alcohols such as ethanol and propanol, water-soluble silicone and the like can be blended as necessary.

【0012】本発明の毛髪脱色剤の剤型は粉末、液体、
クリーム、ゲル、ペースト、エアゾール、エアゾールフ
ォーム、ミスト等の種々の形態を取り得るが、特に、エ
アゾール、エアゾールフォーム等の空気に接触しない剤
型が安定性の点で好ましい。この場合には、公知の噴霧
ガスを用い常法に従って調製することができる。
The hair bleaching agent of the present invention has a dosage form of powder, liquid,
It may take various forms such as cream, gel, paste, aerosol, aerosol foam, mist and the like, and in particular, a dosage form which does not come into contact with air such as aerosol and aerosol foam is preferable in terms of stability. In this case, it can be prepared according to a conventional method using a known atomizing gas.

【0013】[0013]

【実施例】次に、本発明を実施例を挙げて更に具体的に
説明するが、本発明はその要旨を超えない限り、以下の
実施例の記述に制約されるものではない。 実施例1 下記に示す割合で各成分を配合したミスト状の毛髪脱色
剤を調製した。なお、この毛髪脱色剤のpHは3.0で
あった。
EXAMPLES Next, the present invention will be explained more specifically with reference to examples, but the present invention is not limited to the description of the following examples unless it exceeds the gist. Example 1 A mist-like hair decolorizing agent was prepared by mixing the respective components in the proportions shown below. The pH of this hair decolorizing agent was 3.0.

【0014】 ステアリン酸アスコルビル 10.0重量% クエン酸 0.1 〃 プロピレングリコール 10.0 〃 非イオン界面活性剤 10.0 〃 植物抽出液 10.0 〃 精製水 残量 ────────────────────────── 100.0重量% この毛髪脱色剤を用いて脱色効果、毛髪の損傷及び頭皮
への刺激について、各々パネラー試験を行なった効果を
第1表に示す。 比較例1 実施例1の方法において、精製水100%のものを対照
として用いた場合の結果を第1表に示す。 比較例2 実施例1の方法において、比較のために3%過酸化水素
水溶液を用いた場合の結果を表1に示す。
Ascorbyl stearate 10.0% by weight Citric acid 0.1 〃 Propylene glycol 10.0 〃 Nonionic surfactant 10.0 〃 Plant extract 10.0 〃 Purified water Residual amount ─────── ─────────────────── 100.0% by weight Using this hair bleaching agent, a panel test was conducted for bleaching effect, hair damage, and scalp irritation. The effects are shown in Table 1. Comparative Example 1 Table 1 shows the results of the method of Example 1 in which purified water of 100% was used as a control. Comparative Example 2 Table 1 shows the results obtained by using a 3% hydrogen peroxide aqueous solution for comparison in the method of Example 1.

【0015】[0015]

【表1】 [Table 1]

【0016】注)評価方法 (1)脱色効果 各毛髪脱色剤を用い、10名のパネラーから採取した毛
束に塗布し、8時間放置した後、シャンプーを行い、乾
燥した後、下記の基準で評価し、最も多い結果を表に示
した。
Note) Evaluation method (1) Decolorizing effect Each hair decolorizing agent was applied to a hair bundle collected from 10 panelists, allowed to stand for 8 hours, shampooed and dried, and then according to the following criteria. It was evaluated and the most frequent results are shown in the table.

【0017】<評価基準> ◎:元の髪よりもかなり明るくなる。 ○:元の髪よりも明るくなる。 △:元の髪よりもやや明るくなる。<Evaluation Criteria> ⊚: The hair is considerably brighter than the original hair. ○: Brighter than the original hair. Δ: Lighter than the original hair.

【0018】×:元の髪と明るさは変わらない。 (2)毛髪の損傷 上記(1)の脱色操作の前後の毛髪表面を電子顕微鏡
(倍率3000倍)で観察し、毛小皮の損傷の程度を次
の基準で評価し、最も多い結果を表に示した。
X: The brightness is the same as the original hair. (2) Hair damage The surface of the hair before and after the bleaching operation in (1) above is observed with an electron microscope (magnification: 3,000 times), and the degree of damage to the hair scalp is evaluated according to the following criteria. It was shown to.

【0019】○:脱色前と同じで損傷は認められない。 △:毛小皮にわずかに隆起、亀裂、剥離等の損傷が認め
られる。 ×:毛小皮にかなりの隆起、亀裂、剥離等の損傷が認め
られる。 (3)頭皮への刺激 各毛髪脱色剤を10名のパネラーの頭髪に塗布した際
の、頭皮への刺激を次の基準で評価し、最も多い結果を
表に示した。
◯: No damage is observed as in the case before bleaching. Δ: Slight bumps, cracks, peeling, or other damages are recognized on the hair follicles. X: Significant bumps, cracks, peeling and other damages are recognized on the hair follicles. (3) Irritation to the scalp Irritation to the scalp when each hair bleaching agent was applied to the hair of 10 panelists was evaluated according to the following criteria, and the most frequent results are shown in the table.

【0020】○:頭皮への刺激は全くない。 △:頭皮への刺激がややある。 ×:頭皮への刺激がある。 実施例2 パルミチン酸アスコルビル 8.0重量% エタノール 10.0 〃 非イオン界面活性剤 1.0 〃 水溶性シリコーン 1.0 〃 植物抽出液 10.0 〃 酒石酸 0.2 〃 精製水 残量 ──────────────────────────── 100.0重量% 上記のエアゾールフォーム状の毛髪脱色剤を、調製(p
H=3.5)し、これを毛髪に塗布して脱色処理を行な
ったところ、実施例1と同様に優れた脱色効果が得ら
れ、毛髪の損傷及び頭皮への刺激は認められなかった。 実施例3 アスコルビン酸 12.0重量% 非イオン界面活性剤 10.0 〃 セタノール 5.0 〃 キレート剤 0.5 〃 リン酸1水素2ナトリウム 2.0 〃 精製水 残量 ──────────────────────────── 100.0重量% 上記のクリーム状の毛髪脱色剤を調製(pH=6.8)
し、これを毛髪に塗布して脱色処理を行なったところ、
実施例1と同様に優れた脱色効果が得られ、毛髪の損傷
及び頭皮への刺激は認められなかった。
◯: There is no irritation to the scalp. Δ: There is some irritation to the scalp. ×: There is irritation to the scalp. Example 2 Ascorbyl palmitate 8.0% by weight Ethanol 10.0 〃 Nonionic surfactant 1.0 〃 Water-soluble silicone 1.0 〃 Plant extract liquid 10.0 〃 Tartaric acid 0.2 〃 Purified water Residual amount ── ────────────────────────── 100.0% by weight The above-mentioned aerosol foam hair bleaching agent was prepared (p.
H = 3.5), and this was applied to hair for decolorization treatment. As a result, the same excellent decolorization effect as in Example 1 was obtained, and hair damage and irritation to the scalp were not observed. Example 3 Ascorbic acid 12.0% by weight Nonionic surfactant 10.0 〃 Cetanol 5.0 〃 Chelating agent 0.5 〃 Disodium hydrogen phosphate 2.0 〃 Purified water Residual amount ────── ────────────────────── 100.0% by weight Prepare the above-mentioned creamy hair color remover (pH = 6.8)
Then, when this was applied to hair and decolorized,
Similar to Example 1, an excellent decolorizing effect was obtained, and hair damage and irritation to the scalp were not observed.

【0021】[0021]

【発明の効果】本発明によれば、アスコルビン酸又はそ
の誘導体の作用により、適度な毛髪の脱色ができ、しか
も、脱色過程で毛髪を損傷させたり、頭皮に刺激を与え
たりすることはないので、脱色後の毛髪の仕上りが極め
て良好である。また、脱色後に毛髪の明るさが変化する
こともないので好ましい。
EFFECTS OF THE INVENTION According to the present invention, the action of ascorbic acid or a derivative thereof makes it possible to decolorize the hair to a suitable degree, and further, does not damage the hair or irritate the scalp during the decolorization process. The finish of the hair after decolorization is extremely good. Further, the brightness of the hair does not change after decolorization, which is preferable.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 アスコルビン酸又はその誘導体を配合し
たことを特徴とする毛髪脱色剤。
1. A hair bleaching agent comprising ascorbic acid or a derivative thereof.
【請求項2】 有機酸を併用して配合したことを特徴と
する請求項1記載の毛髪脱色剤。
2. The hair bleaching agent according to claim 1, which is blended together with an organic acid.
JP03239743A 1991-09-19 1991-09-19 Hair bleach Expired - Lifetime JP3122182B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP03239743A JP3122182B2 (en) 1991-09-19 1991-09-19 Hair bleach

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP03239743A JP3122182B2 (en) 1991-09-19 1991-09-19 Hair bleach

Publications (2)

Publication Number Publication Date
JPH0578229A true JPH0578229A (en) 1993-03-30
JP3122182B2 JP3122182B2 (en) 2001-01-09

Family

ID=17049276

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3122182B2 (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998050012A1 (en) * 1997-05-02 1998-11-12 Gist-Brocades B.V. Stable vitamin c concentrates
EP0879591A1 (en) * 1997-04-30 1998-11-25 Bristol-Myers Squibb Company Ascorbic and isoascorbic acids to remove or adjust oxidative color in hair
JP2002167311A (en) * 2000-11-30 2002-06-11 Hoyu Co Ltd Method of hair treatment and hair-treatment agent composition
JP2003113057A (en) * 2001-10-05 2003-04-18 Shiseido Co Ltd Solid composition for bleaching
JP2003113056A (en) * 2001-10-05 2003-04-18 Shiseido Co Ltd Solid composition for bleaching
JP2004285050A (en) * 2002-12-18 2004-10-14 L'oreal Sa Cosmetic use of ascorbic acid derivative as bleaching agent
JP2006225328A (en) * 2005-02-18 2006-08-31 Milbon Co Ltd Hair dye removing agent, hair dye removing agent package and method for removing dye from hair
WO2018003625A1 (en) * 2016-06-29 2018-01-04 日光ケミカルズ株式会社 Damaged hair-improving agent and damaged hair-improving cosmetic containing same

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0879591A1 (en) * 1997-04-30 1998-11-25 Bristol-Myers Squibb Company Ascorbic and isoascorbic acids to remove or adjust oxidative color in hair
WO1998050012A1 (en) * 1997-05-02 1998-11-12 Gist-Brocades B.V. Stable vitamin c concentrates
US6183729B1 (en) 1997-05-02 2001-02-06 Cosmoferm B.V. Stable vitamin C concentrates
JP2002167311A (en) * 2000-11-30 2002-06-11 Hoyu Co Ltd Method of hair treatment and hair-treatment agent composition
JP2003113057A (en) * 2001-10-05 2003-04-18 Shiseido Co Ltd Solid composition for bleaching
JP2003113056A (en) * 2001-10-05 2003-04-18 Shiseido Co Ltd Solid composition for bleaching
JP2004285050A (en) * 2002-12-18 2004-10-14 L'oreal Sa Cosmetic use of ascorbic acid derivative as bleaching agent
JP2006225328A (en) * 2005-02-18 2006-08-31 Milbon Co Ltd Hair dye removing agent, hair dye removing agent package and method for removing dye from hair
WO2018003625A1 (en) * 2016-06-29 2018-01-04 日光ケミカルズ株式会社 Damaged hair-improving agent and damaged hair-improving cosmetic containing same
CN109640939A (en) * 2016-06-29 2019-04-16 日光化学株式会社 Damage hair improver and the damage hair improvement cosmetics containing it
JPWO2018003625A1 (en) * 2016-06-29 2019-04-18 日光ケミカルズ株式会社 Damaged hair improving agent and damaged hair improving cosmetic containing the same

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