Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JP5214079B2 - Hair dye composition - Google Patents
[go: Go Back, main page]

JP5214079B2 - Hair dye composition - Google Patents

Hair dye composition Download PDF

Info

Publication number
JP5214079B2
JP5214079B2 JP2000397218A JP2000397218A JP5214079B2 JP 5214079 B2 JP5214079 B2 JP 5214079B2 JP 2000397218 A JP2000397218 A JP 2000397218A JP 2000397218 A JP2000397218 A JP 2000397218A JP 5214079 B2 JP5214079 B2 JP 5214079B2
Authority
JP
Japan
Prior art keywords
hair
hair dye
weight
dye
agent
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.)
Expired - Fee Related
Application number
JP2000397218A
Other languages
Japanese (ja)
Other versions
JP2002193772A (en
Inventor
祐岳 河合
Original Assignee
ホーユー株式会社
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 ホーユー株式会社 filed Critical ホーユー株式会社
Priority to JP2000397218A priority Critical patent/JP5214079B2/en
Publication of JP2002193772A publication Critical patent/JP2002193772A/en
Application granted granted Critical
Publication of JP5214079B2 publication Critical patent/JP5214079B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Cosmetics (AREA)
  • Coloring (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

産業上の利用分野Industrial application fields

本発明は染毛剤に関するもので、詳しくは、毛髪の柔軟性、しっとり感あるいは滑らかさを向上させ、かつ染色堅牢性に優れる染毛剤組成物に関するものである。  The present invention relates to a hair dye, and more particularly to a hair dye composition that improves the flexibility, moist feeling or smoothness of hair and is excellent in dyeing fastness.

従来より、染毛剤としては酸化染料中間体を含有する第1剤と、酸化剤を含有する第2剤よりなる二剤型の酸化染毛剤が広く利用されている。この酸化染毛剤は、無色の低分子の酸化染料中間体を毛髪中に浸透させ、毛髪内部で酸化重合を行わせることにより色素を生成させて染着させるものである。これらの酸化染毛剤は要望に応じた種々の色調に毛髪を染色することができ、しかもその染毛力も優れているので非常に便利なものである。  Conventionally, two-component oxidative hair dyes comprising a first agent containing an oxidative dye intermediate and a second agent containing an oxidant have been widely used as hair dyes. In this oxidative hair dye, a colorless low molecular weight oxidative dye intermediate is infiltrated into hair, and oxidative polymerization is performed inside the hair to produce a dye and dye it. These oxidation hair dyes are very convenient because they can dye hair in various colors according to demands, and also have excellent hair dyeing power.

発明が解決しようとする課題Problems to be solved by the invention

しかしながら、従来の酸化染毛剤では、染毛処理によって毛髪が損傷しがちであったため、毛髪のつややうるおいがなくなったり、染め上がりが不自然な色となり第三者に違和感を与えたり、また、櫛通りが悪く、髪のしなやかさがなくなるといった課題があった。これらの課題を解決するために、しばしば、カチオン性ポリマーが用いられることがあるが、カチオン性ポリマーのみを配合した場合、毛髪との親和性が高いため、過剰に作用して毛髪にゴワつきやパサつきが生じることもあり、十分な解決には至っていない。  However, with conventional oxidative hair dyes, the hair tends to be damaged by the hair dyeing treatment, so that the gloss and moisture of the hair disappears, the dyed color becomes unnatural and gives a strange feeling to a third party, There was a problem that the comb was bad and the hair was not supple. In order to solve these problems, a cationic polymer is often used. However, when only a cationic polymer is blended, it has a high affinity with hair, so it acts excessively and becomes irritating to the hair. It may not be enough to solve the problem.

従って、毛髪のつやや柔軟性を向上させ、さらに自然な染め上がりと十分な堅牢性が得られる染毛剤の開発が望まれていた。  Accordingly, there has been a demand for the development of a hair dye that improves the gloss and flexibility of the hair and that provides a natural dyeing and sufficient fastness.

課題を解決するための手段Means for solving the problem

【課題を解決するための手段】本発明者は、上記実状を鑑み鋭意研究を重ねた結果、両性高分子化合物であるアクリルアミド/アクリル酸/塩化ジアルキルジアリルアンモニウム共重合体と、特定のアニオン性高分子化合物とを組み合わせることにより、上記課題が解決されることを見出し、本発明を完成するに至った。以下、本発明についてさらに詳細に説明する。 Means for Solving the Problems The present inventor has made extensive studies in view of the above-mentioned circumstances, and as a result, has found that an amphoteric polymer acrylamide / acrylic acid / dialkyldiallylammonium chloride copolymer and a specific anionic high The present inventors have found that the above problems can be solved by combining with a molecular compound, and have completed the present invention. Hereinafter, the present invention will be described in more detail.

【発明の実施の形態】本発明の染毛剤組成物は、両性高分子化合物であるアクリルアミド/アクリル酸/塩化ジアルキルジアリルアンモニウム共重合体と、特定のアニオン性高分子化合物を必須とする。さらに酸化染料と酸化剤を配合した組成物が酸化染毛剤組成物であり、酸化染料を配合しなければ毛髪脱色剤となる。また直接染料のみを用いた半永久染毛剤として利用することもできる。 BEST MODE FOR CARRYING OUT THE INVENTION The hair dye composition of the present invention essentially comprises an amphoteric polymer acrylamide / acrylic acid / dialkyldiallylammonium chloride copolymer and a specific anionic polymer compound. Further, a composition containing an oxidative dye and an oxidant is an oxidative hair dye composition, and if no oxidative dye is added, it becomes a hair bleaching agent. It can also be used as a semi-permanent hair dye using only a direct dye.

本発明の染毛剤組成物は、両性高分子化合物を必須とするが、両性高分子化合物としては、両性ターポリマーであるアクリルアミド/アクリル酸/塩化ジアルキルジアリルアンモニウム共重合体が好ましく、具体的には、ポリクォータニウム39(Polyquaternium-39)として知られ、マーコートプラス3330,3331(カルゴン社製)として市販されている化合物が挙げられる。 Although the amphoteric polymer compound is essential for the hair dye composition of the present invention, the amphoteric polymer compound is preferably an amphoteric terpolymer acrylamide / acrylic acid / dialkyldiallylammonium chloride copolymer. Is known as Polyquaternium-39 and is commercially available as Marquat Plus 3330, 3331 (Calgon).

の配合量は0.05〜10重量%、好ましくは0.1〜5重量%である。0.05重量%未満であると十分な効果が得られず、10重量%を超えてもそれ以上効果が上がらない。 The amount of that from 0.05 to 10% by weight, preferably 0.1 to 5 wt%. If it is less than 0.05% by weight, a sufficient effect cannot be obtained, and if it exceeds 10% by weight, the effect is not further improved.

アニオン性高分子化合物は、(a)イタコン酸とポリオキシエチレンアルキルエーテルとの半エステルまたはメタクリル酸とポリオキシエチレンアルキルエーテルとのエステル、及び(b)アクリル酸、メタクリル酸およびそれらのアルキルエステルから選ばれる少なくとも一つのモノマーから成る共重合体から選ばれる1種以上である。これらの化合物は、具体的には例えばAcrylates/Ceteth−20 Itaconate Copolymer、Acrylates/Steareth−20 Itaconate Copolymer、Acrylates/Beheneth−25 Itaconate Copolymer、Acrylates/Ceteth−20Methacrylate Copolymer、Acrylates/Steareth−20 Methacrylate CopolymerあるいはAcrylates/Beheneth−25 Methacrylate Copolymerという名称で知られる。 The anionic polymer compound comprises : ( a) a half ester of itaconic acid and polyoxyethylene alkyl ether or an ester of methacrylic acid and polyoxyethylene alkyl ether; and (b) acrylic acid, methacrylic acid and their alkyl esters. It is at least one selected from a copolymer comprising at least one monomer selected. These compounds, specifically, for example Acrylates / Ceteth-20 Itaconate Copolymer, Acrylates / Steareth-20 Itaconate Copolymer, Acrylates / Beheneth-25 Itaconate Copolymer, Acrylates / Ceteth-20Methacrylate Copolymer, Acrylates / Steareth-20 Methacrylate Copolymer or Acrylates / Beheneth-25 is known under the name of Methacrylate Copolymer.

その配合量は、過酸化水素の安定性に支障のない範囲で配合ができ、好ましくは、0.05〜20重量%であり、経済面から0.1〜10重量%が特に望ましい。  The blending amount can be blended within a range that does not hinder the stability of hydrogen peroxide, preferably 0.05 to 20% by weight, and particularly preferably 0.1 to 10% by weight from the economical aspect.

本発明の染毛剤組物を永久染毛剤とする場合、通常、酸化染料とアルカリ剤を配合した第1剤と、酸化剤を配合した第2剤からなる多剤型の酸化染毛剤組成物となる。そして第1剤に酸化染料を配合しなければ毛髪脱色剤として機能する。  When the hair dye assembly of the present invention is used as a permanent hair dye, it is usually a multi-component oxidative hair dye comprising a first agent containing an oxidizing dye and an alkaline agent and a second agent containing an oxidizing agent. It becomes a composition. And if an oxidation dye is not mix | blended with a 1st agent, it will function as a hair bleaching agent.

第1剤に配合する酸化染料は、通常、主要中間体とカプラーに分けられる。主要中間体としては、フェニレンジアミン類、アミノフェノール類、ジアミノピリジン類等及びそれらの塩類の1種又は2種以上が挙げられる。塩類としては塩酸塩、硫酸塩、酢酸塩等が挙げられる。これらの中でもp−フェニレンジアミン、トルエン−2,5−ジアミン、N,N−ビス(β−ヒドロキシエチル)−p−フェニレンジアミン、2−β−ヒドロキシエチル−p−フェニレンジアミン、N−β−ヒドロキシエチル−N−エチル−p−フェニレンジアミン、N−フェニル−p−フェニレンジアミン、4,4’−ジアミノジフェニルアミン、2−クロロ−p−フェニレンジアミン、N,N−ジメチル−p−フェニレンジアミン、p−アミノフェノール、o−アミノフェノール、p−メチルアミノフェノール、2,6−ジクロロ−p−フェニレンジアミン、p−アミノフェニルスルファミン酸、2,5−ジアミノピリジン及びそれらの塩類が効果および染毛力の点から好ましい。その配合量は染毛用第1剤の全重量に対して0.01〜15重量%であり、0.01重量%よりも少ないと十分な染毛効果が得られず、15重量%を超えても、その効果は変わらず経済的ではない。さらには0.1重量%〜10重量%が好ましく、0.1重量%以上配合することにより、より優れた染毛効果が得られる。一方、10重量%を超えた場合は染毛効果の上昇は少なくなる。  The oxidation dye blended in the first agent is usually divided into a main intermediate and a coupler. Examples of the main intermediate include one or more of phenylenediamines, aminophenols, diaminopyridines, and the like and salts thereof. Examples of the salt include hydrochloride, sulfate, acetate and the like. Among these, p-phenylenediamine, toluene-2,5-diamine, N, N-bis (β-hydroxyethyl) -p-phenylenediamine, 2-β-hydroxyethyl-p-phenylenediamine, N-β-hydroxy Ethyl-N-ethyl-p-phenylenediamine, N-phenyl-p-phenylenediamine, 4,4'-diaminodiphenylamine, 2-chloro-p-phenylenediamine, N, N-dimethyl-p-phenylenediamine, p- Aminophenol, o-aminophenol, p-methylaminophenol, 2,6-dichloro-p-phenylenediamine, p-aminophenylsulfamic acid, 2,5-diaminopyridine and salts thereof are effective and hair dyeing power To preferred. The blending amount is 0.01 to 15% by weight with respect to the total weight of the first agent for hair dyeing, and if it is less than 0.01% by weight, sufficient hair dyeing effect cannot be obtained and exceeds 15% by weight. However, the effect remains the same and is not economical. Furthermore, 0.1 weight%-10 weight% are preferable, and the more superior hair dyeing effect is acquired by mix | blending 0.1 weight% or more. On the other hand, when it exceeds 10% by weight, the increase in the hair dyeing effect is reduced.

また、カプラーとしては、レゾルシン、ピロガロール、カテコール、m−アミノフェノール、m−フェニレンジアミン、2,4−ジアミノフェノール、1,2,4−ベンゼントリオール、トルエン−3,4−ジアミン、トルエン−2,4−ジアミン、ハイドロキノン、α−ナフトール、2,6−ジアミノピリジン、1,5−ジヒドロキシナフタレン、5−アミノ−o−クレゾール、ジフェニルアミン、p−メチルアミノフェノール、フロログルシン、2,4−ジアミノフェノキシエタノール、没食子酸、タンニン酸、没食子酸エチル、没食子酸メチル、没食子酸プロピル、五倍子、1−メトキシ−2−アミノ−4−(2−ヒドロキシエチル)アミノベンゼン、5−(2−ヒドロキシエチルアミノ)−2−メチルフェノ−ル等及びそれらの塩を配合することができる。この配合量は0.01〜10重量%であり、0.01重量%よりも少ないと十分な染色性が得られず、10重量%を超えても、その効果は変わらず経済的ではない。さらには、0.1重量%〜5重量%が好ましく、0.1重量%以上配合することにより、より優れた染色性が得られる。一方、5重量%を超えた場合は染色性の上昇は少なくなる。その他、「医薬部外品原料規格」(1991年6月発行,薬事日報社)に収載されたものも適宜、用いることができる。  As couplers, resorcin, pyrogallol, catechol, m-aminophenol, m-phenylenediamine, 2,4-diaminophenol, 1,2,4-benzenetriol, toluene-3,4-diamine, toluene-2, 4-diamine, hydroquinone, α-naphthol, 2,6-diaminopyridine, 1,5-dihydroxynaphthalene, 5-amino-o-cresol, diphenylamine, p-methylaminophenol, phloroglucin, 2,4-diaminophenoxyethanol, gallic acid Acid, tannic acid, ethyl gallate, methyl gallate, propyl gallate, pentaploid, 1-methoxy-2-amino-4- (2-hydroxyethyl) aminobenzene, 5- (2-hydroxyethylamino) -2- Methylphenol etc. and their salts It is possible to focus. The blending amount is 0.01 to 10% by weight, and if it is less than 0.01% by weight, sufficient dyeability cannot be obtained, and even if it exceeds 10% by weight, the effect is not changed and it is not economical. Furthermore, 0.1 weight%-5 weight% is preferable, and the more outstanding dyeability is obtained by mix | blending 0.1 weight% or more. On the other hand, when it exceeds 5% by weight, the increase in dyeability is reduced. In addition, those listed in "Quasi-drug raw material standards" (issued in June 1991, Yakuji Nippo) can be used as appropriate.

さらに、本発明の染毛剤には調色剤として直接染料が配合でき、タール系色素や天然色素などの公知のものを1種又は2種以上併用できる。その中でも、ニトロ系染料、アゾ染料、ニトロソ染料、トリフェニルメタン染料、キサンチン染料、キノリン染料、アントラキノン染料又はインジゴ染料が、良好な染毛効果を得られ好ましく、また、これらの染料を染毛剤組成物中に0.01〜10重量%配合するのが最も良い。0.01重量%より少ない場合、染毛効果は不十分であり、逆に10重量%より多い場合には、染毛力が向上しないばかりか頭皮、手指への染着が著しくなり望ましくない。  Furthermore, the hair dye of the present invention can be blended with a direct dye as a toning agent, and one or more known ones such as tar-based pigments and natural pigments can be used in combination. Among them, nitro dyes, azo dyes, nitroso dyes, triphenylmethane dyes, xanthine dyes, quinoline dyes, anthraquinone dyes or indigo dyes are preferable because they give a good hair dyeing effect, and these dyes are used as hair dyes. It is best to blend 0.01 to 10% by weight in the composition. When the amount is less than 0.01% by weight, the hair dyeing effect is insufficient. On the other hand, when the amount is more than 10% by weight, not only the hair dyeing power is not improved, but also the dyeing to the scalp and fingers is remarkable.

直接染料の具体例としては、ニトロ−p−フェニレンジアミン、p−ニトロ−O−フェニレンジアミン、p−ニトロ−m−フェニレンジアミン、2−アミノ−4−ニトロフェノ−ル、2−アミノ−5−ニトロフェノ−ル、ピクラミン酸、それらの塩および「医薬品等に使用することができるタール色素を定める省令」(昭和41年告示、厚生省)により定められた染料が挙げられる。  Specific examples of the direct dye include nitro-p-phenylenediamine, p-nitro-O-phenylenediamine, p-nitro-m-phenylenediamine, 2-amino-4-nitrophenol, and 2-amino-5-nitrophenol. -Dye specified by the ordinance for determining tar pigments that can be used for pharmaceuticals, etc. (announced in 1966, Ministry of Health and Welfare).

アルカリ剤としては、酸化染毛剤に通常使用されるものでよく、例えばエタノールアミン、ジエタノールアミン、トリエタノールアミン、イソプロパノールアミン及び2−アミノ−2−メチル−1−プロパノ−ル等のアルカノールアミン類やアンモニアが挙げられる。  Alkaline agents may be those usually used for oxidative hair dyes, such as alkanolamines such as ethanolamine, diethanolamine, triethanolamine, isopropanolamine and 2-amino-2-methyl-1-propanol. Ammonia is mentioned.

さらに、この第1剤には本発明の効果を妨げない範囲において、従来公知の成分を添加配合することができる。例えば、流動パラフィンやワセリン等の炭化水素類、高級アルコール、エステル油、脂肪酸、シリコーンおよびその誘導体、多価アルコール、紫外線吸収剤、防腐剤、界面活性剤、増粘剤、pH調整剤、アルカリ剤、香料、パール化剤などが挙げられる。  Furthermore, conventionally known components can be added and blended with the first agent within a range that does not hinder the effects of the present invention. For example, hydrocarbons such as liquid paraffin and petrolatum, higher alcohols, ester oils, fatty acids, silicones and derivatives thereof, polyhydric alcohols, ultraviolet absorbers, preservatives, surfactants, thickeners, pH adjusters, alkaline agents , Fragrance, pearlizing agent and the like.

一方、第2剤に配合する酸化剤は、通常、過酸化水素が用いられる。  On the other hand, hydrogen peroxide is usually used as the oxidizing agent to be blended with the second agent.

これらの他、必要に応じて高級アルコール、多価アルコール、界面活性剤、高分子物質、pH調整剤、金属封鎖剤、酸化防止剤、アミノ酸、香料、防腐剤、抗炎剤、着色料等を配合しても良く、それらは公知のものを広く使用できる。  In addition to these, higher alcohols, polyhydric alcohols, surfactants, polymer substances, pH adjusters, sequestering agents, antioxidants, amino acids, fragrances, preservatives, anti-flame agents, coloring agents, etc. You may mix | blend and they can use a well-known thing widely.

本発明の染毛剤組成物を、半永久染毛剤とする場合には、上述の直接染料のみが使用され、さらに染色促進剤としてエタノールなどの低級アルコール、ベンジルアルコールなどの芳香族アルコール、アルキレンカーボネート、N−メチルピロリドンあるいはレブリン酸等の各種溶剤が配合される。その他、必要に応じて高級アルコール、多価アルコール、界面活性剤、高分子物質、pH調整剤、金属封鎖剤、酸化防止剤、アミノ酸、香料、防腐剤、抗炎剤、着色料等を配合しても良く、それらは公知のものを広く使用できる。  When the hair dye composition of the present invention is used as a semi-permanent hair dye, only the above-mentioned direct dyes are used. Further, lower alcohols such as ethanol, aromatic alcohols such as benzyl alcohol, alkylene carbonates as dyeing accelerators. Various solvents such as N-methylpyrrolidone or levulinic acid are blended. In addition, higher alcohols, polyhydric alcohols, surfactants, polymer substances, pH adjusters, sequestering agents, antioxidants, amino acids, fragrances, preservatives, anti-flame agents, coloring agents, etc. These may be widely used.

本発明の染毛剤組成物の剤型としては、液状、乳液状、クリーム状、ゲル状あるいはエアゾール泡沫状など、通常知られている形態をとることができる。  As the dosage form of the hair dye composition of the present invention, it is possible to take a commonly known form such as liquid, emulsion, cream, gel or aerosol foam.

次に本発明を実施例を挙げて詳細に説明するが、本発明は以下の実施例により限定されるものではない。  EXAMPLES Next, although an Example is given and this invention is demonstrated in detail, this invention is not limited by a following example.

表1に酸化染毛剤組成物の第1剤及び第2剤の配合例を示す。また表2に、これら第1剤及び第2剤の組合せによる実施例1および比較例1〜5を示す。  Table 1 shows formulation examples of the first agent and the second agent of the oxidative hair dye composition. Table 2 shows Example 1 and Comparative Examples 1 to 5 based on a combination of these first and second agents.

Figure 0005214079
Figure 0005214079

Figure 0005214079
Figure 0005214079

<染毛試験>
各組成物を常法にて調製した。染毛試験は、比較例5を対照とし、パネラーを用いてハーフヘッドで染毛比較を行った。染毛剤第1剤と第2剤を重量比1:1で混合し、頭髪に塗布後、30分放置し、シャンプーで洗浄後、ドライヤーで乾燥した。仕上がりの感触は、毛髪の柔らかさ、しっとり感及び滑らかさなどを総合的に、また色持ちは1ヶ月後の状態を目視により、以下の基準で評価した。
<Hair dyeing test>
Each composition was prepared in a conventional manner. In the hair dyeing test, Comparative Example 5 was used as a control, and a hair dye was compared with a half head using a panel. The first and second hair dyes were mixed at a weight ratio of 1: 1, applied to the hair, left for 30 minutes, washed with shampoo, and dried with a dryer. The feel of the finish was evaluated based on the following criteria by comprehensively evaluating the softness, moistness and smoothness of the hair, and the color retention was visually observed after one month.

<評価基準>
○:比較例5に比べ、非常に良い。
△:比較例5に比べ、やや良い。
×:比較例5と同等。
これらの結果を表2に示す。
<Evaluation criteria>
○: Very good as compared with Comparative Example 5.
Δ: Slightly better than Comparative Example 5.
X: Equivalent to Comparative Example 5.
These results are shown in Table 2.

表2に示す結果から分かるように、実施例1はいずれの評価も良好であった。  As can be seen from the results shown in Table 2, Example 1 was good in all evaluations.

実施例2及び比較例6
実施例2(酸性染毛料組成物)

Figure 0005214079
Example 2 and Comparative Example 6
Example 2 (acid hair dye composition)
Figure 0005214079

Figure 0005214079
※1:アクリルアミド・アクリル酸・塩化ジメチルジアリルアンモニウム共重合体(カルゴン社製)
Figure 0005214079
* 1: Acrylamide / acrylic acid / dimethyldiallylammonium chloride copolymer (Calgon)

上記実施例2から両性高分子化合物(マーコートプラス3331)及びアニオン性高分子化合物(Acrylates/Ceteth-20 Itaconate Copolymer)を除いただけの組成物を比較例6とし、各成分を室温にて精製水に順次溶解し、二剤式酸性染毛料を得た。そして第1剤を毛髪に塗布後、40℃程度に加温しながら10分間程度放置した後、第2剤を毛髪に塗布し、さらに45℃にて10分間程度放置した後、これを水で充分に洗い流すことにより、染毛を行った。その結果、仕上がりの感触と色持ちは、比較例6に比べ、非常に良好であった。  The composition obtained by removing the amphoteric polymer compound (Mercoat Plus 3331) and the anionic polymer compound (Acrylates / Ceteth-20 Itaconate Copolymer) from Example 2 was used as Comparative Example 6, and each component was added to purified water at room temperature. Dissolving sequentially, a two-component acidic hair dye was obtained. Then, after applying the first agent to the hair, let it stand for about 10 minutes while warming to about 40 ° C., then apply the second agent to the hair and leave it at 45 ° C. for about 10 minutes, and then wash it with water. The hair was dyed by washing thoroughly. As a result, the finished feel and color were very good as compared with Comparative Example 6.

実施例3(エアゾール泡沫状酸化染毛剤)

Figure 0005214079
Example 3 (aerosol foamy oxidative hair dye)
Figure 0005214079

Figure 0005214079
Figure 0005214079

上記原液と噴射剤(LPG3.5)を96:4の比率でエアゾール缶に充填し、染毛剤組成物を得た。常法により染毛し、その結果、実施例1と同様に、良好な仕上がりの感触と色持ちが得られた。  The stock solution and the propellant (LPG3.5) were filled in an aerosol can at a ratio of 96: 4 to obtain a hair dye composition. The hair was dyed by a conventional method, and as a result, as in Example 1, a good finished feel and color persistence were obtained.

以下に本件発明の処方例を示す。
<第1剤処方>

Figure 0005214079
※2:ヒドロキシエチルヒドロキシプロピルトリメチルアンモニウムクロリドエーテル(ライオン社製)The prescription example of this invention is shown below.
<First drug formulation>
Figure 0005214079
* 2: Hydroxyethylhydroxypropyltrimethylammonium chloride ether (manufactured by Lion)

Figure 0005214079
Figure 0005214079

Figure 0005214079
Figure 0005214079

<第2剤処方>

Figure 0005214079
<Second drug formulation>
Figure 0005214079

Figure 0005214079
Figure 0005214079

Figure 0005214079
Figure 0005214079

上述の第1〜2剤を常法にて調製した。これら染毛剤組成物第1剤と第2剤を適宜組み合わせて、実施例1と同様に試験したところ、仕上がりの感触や色持ちに優れた効果を示した。  The above-mentioned first and second agents were prepared by a conventional method. When these hair dye composition 1st agent and 2nd agent were combined suitably and it tested similarly to Example 1, the effect excellent in the feel of a finish and color retention was shown.

発明の効果Effect of the invention

毛髪の柔軟性、しっとり感あるいは滑らかさを向上させ、かつ染色堅牢性に優れる染毛剤組成物を提供することができる。  It is possible to provide a hair dye composition that improves the flexibility, moist feeling or smoothness of hair and is excellent in dyeing fastness.

Claims (2)

アクリルアミド/アクリル酸/塩化ジアルキルジアリルアンモニウム共重合体と、(a)イタコン酸とポリオキシエチレンアルキルエーテルとの半エステルまたはメタクリル酸とポリオキシエチレンアルキルエーテルとのエステル、及び(b)アクリル酸、メタクリル酸およびそれらのアルキルエステルから選ばれる少なくとも一つのモノマーから成る共重合体から選ばれる1種以上であるアニオン性高分子化合物を含有することを特徴とする染毛剤組成物。
An acrylamide / acrylic acid / dialkyldiallylammonium chloride copolymer , (a) a half ester of itaconic acid and polyoxyethylene alkyl ether, or an ester of methacrylic acid and polyoxyethylene alkyl ether, and (b) acrylic acid, methacrylic acid A hair dye composition comprising at least one anionic polymer compound selected from a copolymer comprising at least one monomer selected from acids and alkyl esters thereof.
アルカリ剤と、アクリルアミド/アクリル酸/塩化ジアルキルジアリルアンモニウム共重合体を含有する第1剤と、過酸化水素及び(a)イタコン酸とポリオキシエチレンアルキルエーテルとの半エステルまたはメタクリル酸とポリオキシエチレンアルキルエーテルとのエステル、及び(b)アクリル酸、メタクリル酸およびそれらのアルキルエステルから選ばれる少なくとも一つのモノマーから成る共重合体から選ばれる1種以上であるアニオン性高分子化合物を含有する第2剤からなることを特徴とする請求項1に記載の染毛剤組成物。 Alkaline agent, first agent containing acrylamide / acrylic acid / dialkyldiallylammonium chloride copolymer , hydrogen peroxide and (a) half ester of itaconic acid and polyoxyethylene alkyl ether or methacrylic acid and polyoxyethylene A second containing an ester with an alkyl ether, and (b) one or more anionic polymer compounds selected from a copolymer consisting of at least one monomer selected from acrylic acid, methacrylic acid and their alkyl esters The hair dye composition according to claim 1, comprising a hair dye.
JP2000397218A 2000-12-27 2000-12-27 Hair dye composition Expired - Fee Related JP5214079B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2000397218A JP5214079B2 (en) 2000-12-27 2000-12-27 Hair dye composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000397218A JP5214079B2 (en) 2000-12-27 2000-12-27 Hair dye composition

Publications (2)

Publication Number Publication Date
JP2002193772A JP2002193772A (en) 2002-07-10
JP5214079B2 true JP5214079B2 (en) 2013-06-19

Family

ID=18862372

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000397218A Expired - Fee Related JP5214079B2 (en) 2000-12-27 2000-12-27 Hair dye composition

Country Status (1)

Country Link
JP (1) JP5214079B2 (en)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004091359A (en) * 2002-08-30 2004-03-25 Kanebo Ltd Aerosol type creamy hair dye agent
JP2004091355A (en) * 2002-08-30 2004-03-25 Kanebo Ltd Simultaneously spraying type creamy hair dye composition
JP3520078B1 (en) 2003-02-26 2004-04-19 ホーユー株式会社 Depigmenting composition and hair coloring composition
DE102004018723A1 (en) * 2004-04-17 2005-11-03 Wella Ag Itaconic acid monoester / acrylate copolymer and polystyrenesulfonate containing hair treatment agent
WO2006060568A1 (en) 2004-12-02 2006-06-08 The Procter & Gamble Company Thickened hair colourant and bleaching compositions
CA2588373A1 (en) * 2004-12-02 2006-06-08 The Procter & Gamble Company Polymer thickened hair colouring and bleaching compositions
JP4950749B2 (en) * 2006-04-25 2012-06-13 花王株式会社 Hair cosmetics
EP1878469B1 (en) 2006-07-12 2010-09-01 The Procter & Gamble Company Gel network surfactant based thickening systems for hair colourant and bleaching compositions
JP5530588B2 (en) * 2007-06-14 2014-06-25 ホーユー株式会社 Hair elasticity improver
TWI407973B (en) * 2008-05-30 2013-09-11 Kao Corp Two-part foam hair dye
JP5824763B2 (en) * 2010-11-18 2015-12-02 株式会社マンダム Decoloring agent or oxidative hair dye, and method for decoloring or dyeing hair
JP5824764B2 (en) * 2010-11-18 2015-12-02 株式会社マンダム Decoloring agent or oxidative hair dye, and method for decoloring or dyeing hair
JP5875257B2 (en) * 2011-06-15 2016-03-02 株式会社ミルボン Method for producing oxidative hair dye
US9226879B2 (en) * 2011-09-30 2016-01-05 L'oreal Foam dye composition comprising at least one particular oxyethylenated nonionic surfactant
JP5907608B2 (en) * 2012-01-13 2016-04-26 株式会社ミルボン Multi-agent hair treatment
JP6124660B2 (en) * 2013-04-18 2017-05-10 株式会社ミルボン Oxidizing hair treatment agent
BR112015030531B1 (en) 2013-06-05 2020-10-06 Kao Corporation CAPILLARY COSMETICS AND ITS USE
EP3108872B2 (en) 2014-02-17 2021-09-15 Kao Corporation Hair cosmetic
JP6410336B2 (en) * 2014-02-17 2018-10-24 花王株式会社 Decolorization or hair dye composition
EP2957324B1 (en) * 2014-06-17 2017-09-27 Noxell Corporation A cosmetic composition comprising a thickening polymer having hydrophobic and hydrophilic portions

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3890161B2 (en) * 1999-04-15 2007-03-07 ホーユー株式会社 Oxidative hair dye composition

Also Published As

Publication number Publication date
JP2002193772A (en) 2002-07-10

Similar Documents

Publication Publication Date Title
JP5214079B2 (en) Hair dye composition
JP6873994B2 (en) Composition for treating hair
CN103781465B (en) Method for pigmented hair
JP5296329B2 (en) Oxidative hair dye or decolorant composition
JP2000297019A (en) Oxidation hair-dyeing agent composition
WO2013136480A1 (en) Hair dye and hair dyeing method
CN102223872A (en) Hair cosmetic composition
JP2004075644A (en) Hair dye composition
JP4718063B2 (en) Oxidizing agent composition, hair dyeing agent or hair bleaching agent
JP2011102244A (en) Hair treating agent
JP4551545B2 (en) Oxidative hair dye composition
JP3992404B2 (en) Foam hair dye composition
JP2025185265A (en) Hair dye composition
JP5506285B2 (en) Hair treatment agent
JP2010018569A (en) Hair cosmetic composition
JP3926057B2 (en) Oxidative hair dye composition and hair treatment composition for hair dyeing
JP2007145783A (en) Hair dye composition
JP2005239627A (en) Hair dye composition
JP7396622B2 (en) Oxidative hair dye composition and hair dyeing method
JP2003119116A (en) Method and kit for treating hair
JP2011042584A (en) Hair-treating method and hair-treating kit
JP3932483B2 (en) Oxidative hair dye for temporary hair color restoration and hair dyeing method
JP5439090B2 (en) Hair treatment agent
JP5005276B2 (en) Multi-agent hair treatment agent and method of using the same
JP2016088891A (en) Oxidative hair dye

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20070803

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20081029

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20100413

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20100614

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20101102

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20130227

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

Ref document number: 5214079

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20160308

Year of fee payment: 3

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees