JPH09323921A - Hair dyeing composition - Google Patents
Hair dyeing compositionInfo
- Publication number
- JPH09323921A JPH09323921A JP18430896A JP18430896A JPH09323921A JP H09323921 A JPH09323921 A JP H09323921A JP 18430896 A JP18430896 A JP 18430896A JP 18430896 A JP18430896 A JP 18430896A JP H09323921 A JPH09323921 A JP H09323921A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- weight
- hair
- hair dye
- dye composition
- 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
Links
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- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、染着性、耐洗髪性、安
定性に優れた染毛料組成物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a hair dye composition having excellent dyeing properties, wash resistance and stability.
【0002】[0002]
【従来の技術】従来汎用されている酸化染毛料は、使用
時にアルカリ性下で過酸化水素水を作用させるために、
扱い方によっては毛髪損傷や一次皮膚刺激を引き起こす
危険性がある。このため頭皮や頭髪に対して影響の少な
い酸性染料を用いた酸性染毛料が開発されてきた。しか
しながら、市販されている酸性染毛料は、酸化染毛剤に
比べ、染着性、耐洗髪性、安定性の点で満足のいくもの
ではなかった。2. Description of the Related Art Oxidized hair dyes that have been widely used in the past are used in order to make hydrogen peroxide act under alkaline conditions during use.
There is a risk of causing hair damage and primary skin irritation depending on the treatment method. For this reason, acidic hair dyes have been developed that use acidic dyes that have little effect on the scalp and hair. However, the commercially available acidic hair dye is not satisfactory in terms of dyeing property, hair wash resistance and stability as compared with the oxidative hair dye.
【0003】[0003]
【発明が解決しようとする課題】本発明は、染着性、耐
洗髪性、安定性に優れた染毛料組成物を提供することを
目的とする。SUMMARY OF THE INVENTION It is an object of the present invention to provide a hair dye composition which is excellent in dyeing property, hair wash resistance and stability.
【0004】[0004]
【課題を解決するための手段】本発明者は、種々検討し
た結果(1)アルキル基の炭素数が10〜30であるア
クリル酸・メタクリル酸アルキル共重合体を単独もしく
はポリビニルアルコールと組み合わせたものを用いるこ
とによって、(2)ベンジルアルコール、n−ブタノー
ル、シクロヘキサノール、フェノキシエタノール、ベン
ジルオキシエタノールの中から選ばれる一種もしくは二
種以上の一価アルコールを分散させ、さらに(3)酸
と、(4)酸性染料とを配合し、かつpHを1.5〜
4.5に調整することにより得られた染毛料組成物は染
着性、耐洗髪性、安定性に優れていることを見出し本発
明を完成するに至った。Means for Solving the Problems As a result of various studies by the present inventor, (1) an acrylic acid / alkyl methacrylate copolymer having an alkyl group having 10 to 30 carbon atoms, alone or in combination with polyvinyl alcohol By using (2), one or more monohydric alcohols selected from (2) benzyl alcohol, n-butanol, cyclohexanol, phenoxyethanol and benzyloxyethanol are dispersed, and (3) acid and (4) ) Mixing with an acid dye and adjusting the pH to 1.5-
The inventors have found that the hair dye composition obtained by adjusting to 4.5 is excellent in dyeing property, hair wash resistance and stability, and completed the present invention.
【0005】以下に、本発明を詳細に説明する。The present invention will be described in detail below.
【0006】本発明に用いられる(1)アルキル基の炭
素数が10〜30であるアクリル酸・メタクリル酸アル
キル共重合体としてはPEMUREN TR−1、PE
MUREN TR−2(いづれもBFGoodrich
社製商品名)等、ポリビニルアルコールとしては例えば
ゴーセノールEGシリーズ(日本合成化学工業株式会社
製品名)等が挙げられ、その配合量は総量で0.05〜
15重量%であり、好ましくは0.2〜10重量%であ
る。0.05重量%未満では一価アルコールを充分に分
散できず、また15重量%を超えて配合しても流動性が
なくなり使用性に難がある。The (1) alkyl acrylate / alkyl methacrylate copolymers having an alkyl group of 10 to 30 carbon atoms used in the present invention include PEMUREN TR-1 and PE.
MUREN TR-2 (Both Goodrich BFGoodrich
Examples of polyvinyl alcohol include Goshenol EG series (product name of Nippon Synthetic Chemical Industry Co., Ltd.) and the like, and the total amount thereof is from 0.05 to
It is 15% by weight, preferably 0.2 to 10% by weight. If it is less than 0.05% by weight, the monohydric alcohol cannot be sufficiently dispersed, and if it exceeds 15% by weight, the fluidity is lost and the usability is poor.
【0007】本発明に用いられる(2)ベンジルアルコ
ール、n−ブタノール、シクロヘキサノール、フェノキ
シエタノール、ベンジルオキシエタノールの中から選ば
れる一種もしくは二種以上の一価アルコールの配合量は
1〜30重量%であり、好ましくは2〜20重量%であ
る。1重量%未満では充分な染着効果が発揮されず、ま
た30重量%を超えて配合しても染着効果の向上に顕著
な差がでなくなる。The blending amount of (2) one or more monohydric alcohols selected from the group consisting of benzyl alcohol, n-butanol, cyclohexanol, phenoxyethanol and benzyloxyethanol used in the present invention is 1 to 30% by weight. %, Preferably 2 to 20% by weight. If it is less than 1% by weight, a sufficient dyeing effect is not exerted, and if it exceeds 30% by weight, there is no significant difference in improvement of the dyeing effect.
【0008】本発明に用いられる(3)酸としては、グ
リコール酸、乳酸、クエン酸、酒石酸、リンゴ酸等の有
機酸及びリン酸、塩酸等の無機酸が挙げられ、その配合
量は0.1〜10重量%であり、好ましくは0.2〜7
重量%である。0.1重量%未満では充分な染着効果が
発揮されず、また10重量%を超えて配合しても染着効
果の向上に顕著な差がでなくなる。またpH調整剤とし
て上記酸の塩を用いることもできる。Examples of the (3) acid used in the present invention include organic acids such as glycolic acid, lactic acid, citric acid, tartaric acid and malic acid, and inorganic acids such as phosphoric acid and hydrochloric acid, and the blending amount thereof is 0. 1 to 10% by weight, preferably 0.2 to 7
% By weight. If it is less than 0.1% by weight, a sufficient dyeing effect is not exhibited, and if it exceeds 10% by weight, there is no significant difference in the improvement of the dyeing effect. Further, a salt of the above acid can be used as a pH adjuster.
【0009】本発明に用いられる(4)酸性染料として
は、人体に有害な影響を及ぼさない「医薬品等に使用す
ることのできるタール色素を定める省令」によって定め
られた法定色素の中から選ばれる一種もしくは二種以上
を組み合わせて用いることができる。その配合量は0.
001〜2重量%であり、好ましくは0.05〜1重量
%である。0.001重量%未満では充分な染着効果が
発揮されず、また2重量%を超えて配合しても染着効果
の向上に顕著な差がでなくなる。The acid dye (4) used in the present invention is selected from legal dyes defined by "Ministerial Ordinance for Defining Tar Dyes that can be Used in Pharmaceuticals" that does not have a harmful effect on the human body. One kind or a combination of two or more kinds can be used. The blending amount is 0.
It is 001 to 2% by weight, preferably 0.05 to 1% by weight. If it is less than 0.001% by weight, a sufficient dyeing effect is not exhibited, and if it exceeds 2% by weight, there is no significant difference in improvement of the dyeing effect.
【0010】本発明の染毛料組成物には、系の安定性、
pHの値を損なわない範囲であれば、上記の成分の他に
炭化水素、油脂、エステル、高級アルコール、シリコン
類、非イオン性界面活性剤、陰イオン性界面活性剤、両
性界面活性剤、増粘剤、防腐剤、キレート剤、香料等を
配合することができる。The hair dye composition of the present invention has a system stability,
In addition to the above components, hydrocarbons, oils and fats, esters, higher alcohols, silicones, nonionic surfactants, anionic surfactants, amphoteric surfactants, and amphoteric surfactants, and A viscous agent, a preservative, a chelating agent, a perfume, etc. can be added.
【0011】また、本発明の染毛料組成物は、本発明の
効果を損なわない範囲内で、所望の形態にすることがで
きる。例えば、増粘剤を配合するこにより乳液状からク
リーム状までの任意の粘性をもたせることができる。Further, the hair dye composition of the present invention can be formed into a desired form within a range that does not impair the effects of the present invention. For example, by adding a thickening agent, it can have any viscosity from emulsion to cream.
【0012】本発明に用いられる増粘剤の具体例として
は、ヒドロキシエチルセルロース、カルボキシメチルセ
ルロース、ヒドロキシプロピルメチルセルロース、キサ
ンタンガム、プルラン、ペクチン、タマリンド種子、ト
ラガントガム、アラビアガム、アルギン酸ナトリウム等
の水溶性高分子が挙げられ、それぞれを単独もしくは二
種以上を組み合わせて使用することができる。その配合
量は0.2〜10重量%であり、好ましくは0.5〜5
重量%である。0.2重量%未満では充分な粘性効果が
発揮されず、また10重量%を超えて配合しても流動性
がなくなり使用性に難がある。Specific examples of the thickener used in the present invention include water-soluble polymers such as hydroxyethyl cellulose, carboxymethyl cellulose, hydroxypropylmethyl cellulose, xanthan gum, pullulan, pectin, tamarind seed, tragacanth gum, gum arabic, and sodium alginate. Each of these can be used alone or in combination of two or more. The blending amount is 0.2 to 10% by weight, preferably 0.5 to 5
% By weight. If it is less than 0.2% by weight, sufficient viscous effect is not exhibited, and if it exceeds 10% by weight, fluidity is lost and usability is poor.
【0013】また、本発明の染毛料組成物は、非イオン
性界面活性剤、陰イオン性界面活性剤、両性界面活性剤
中から選ばれる一種もしくは二種以上の起泡剤と噴射ガ
スを組み合わせることにより泡状エアゾール製剤にする
ことができる。Further, the hair dye composition of the present invention comprises a combination of a propellant gas and one or more foaming agents selected from nonionic surfactants, anionic surfactants and amphoteric surfactants. Thus, a foam aerosol preparation can be obtained.
【0014】[0014]
【実施例】次に、本発明の実施例について説明する。EXAMPLES Next, examples of the present invention will be described.
【0015】表1の実施例1〜4及び表2比較例1〜4
の染毛料組成物を製造し、それぞれについて白髪混じり
の人毛毛束に塗布し、常温で10分間放置後、市販のシ
ャンプーで洗浄し、乾燥させ染着性の評価を行った。Examples 1 to 4 in Table 1 and Comparative Examples 1 to 4 in Table 2
Each of the hair dye compositions was prepared and applied to a human hair bundle containing white hair, left at room temperature for 10 minutes, washed with a commercially available shampoo, and dried to evaluate the dyeability.
【0016】また、表1の実施例1〜4及び表2比較例
1〜4の染毛料組成物それぞれについて白髪混じりの人
毛毛束に塗布し、常温で10分間放置後、市販のシャン
プーで洗浄し、乾燥させる。この染毛毛束を市販のシャ
ンプーで洗浄、乾燥を20回繰り返した後の染毛毛束と
比較して耐洗髪性の効果の評価を行った。Each of the hair dye compositions of Examples 1 to 4 in Table 1 and Comparative Examples 1 to 4 in Table 2 was applied to a human hair bundle containing white hair, left at room temperature for 10 minutes, and then washed with a commercially available shampoo. And dry. This hair bundle was washed with a commercially available shampoo and dried 20 times, and compared with a hair bundle after repeated 20 times to evaluate the effect of hair wash resistance.
【0017】また、表1の実施例1〜4及び表2比較例
1〜4の染毛料組成物それぞれについて保温器中で40
℃に保ちながら3ヶ月にわたって安定性を評価した。Further, each of the hair dye compositions of Examples 1 to 4 in Table 1 and Comparative Examples 1 to 4 in Table 2 was 40
Stability was evaluated for 3 months while maintaining at 0 ° C.
【0018】[0018]
【表1】実施例 評価基準 ◎:非常に良い ○:良い △:あまり良くない ×:悪い 以下余白[Table 1] Examples Evaluation criteria ◎: Very good ○: Good △: Not very good ×: Poor margin below
【0019】[0019]
【表2】比較例 評価基準 ◎:非常に良い ○:良い △:あまり良くない ×:悪い[Table 2] Comparative example Evaluation criteria ◎: Very good ○: Good △: Not very good ×: Bad
【0020】表1及び表2から、アクリル酸・メタクリ
ル酸アルキル共重合体及を欠くと安定性が劣り、ベンジ
ルアルコールもしくは酸を欠くと染着性、耐洗髪性が劣
ることがわかる。From Tables 1 and 2, it can be seen that lack of acrylic acid / alkyl methacrylate copolymer results in poor stability, and lack of benzyl alcohol or acid results in poor dyeing property and hair wash resistance.
【0021】 [0021]
【0022】実施例5の泡状エアゾール染毛料組成物は
良好な泡を形成し、白髪混じりの人毛毛束に塗布して常
温で10分間放置後、市販のシャンプーで洗浄し、乾燥
させ染着性の評価を行ったところ、優れた染着性を示し
た。The foamed aerosol hair dye composition of Example 5 formed a good foam, was applied to a human hair bundle containing white hair, allowed to stand at room temperature for 10 minutes, washed with a commercial shampoo, dried and dyed. When it was evaluated for its properties, it showed excellent dyeing properties.
【0023】[0023]
【発明の効果】本発明によれば、染着性、耐洗髪性、安
定性に優れた染毛料組成物を得ることができる。According to the present invention, it is possible to obtain a hair dye composition having excellent dyeing properties, hair wash resistance and stability.
Claims (5)
であるアクリル酸・メタクリル酸アルキル共重合体を単
独もしくはポリビニルアルコールと組み合わせたもの
と、(2)ベンジルアルコール、n−ブタノール、シク
ロヘキサノール、フェノキシエタノール、ベンジルオキ
シエタノールの中から選ばれる一種もしくは二種以上の
一価アルコールと、(3)酸と、(4)酸性染料を含有
し、かつpHが1.5〜4.5であることを特徴とする
染毛料組成物。1. A carbon number of (1) an alkyl group is 10 to 30.
And one or more selected from the group consisting of (2) benzyl alcohol, n-butanol, cyclohexanol, phenoxyethanol, and benzyloxyethanol. A hair dye composition containing the monohydric alcohol, (3) acid, and (4) acid dye, and having a pH of 1.5 to 4.5.
であるアクリル酸・メタクリル酸アルキル共重合体を単
独もしくはポリビニルアルコールと組み合わせたものの
配合量が0.05〜15重量%である請求項1記載の染
毛料組成物。2. (1) The alkyl group has 10 to 30 carbon atoms.
The hair dye composition according to claim 1, wherein the compounding amount of the acrylic acid / alkyl methacrylate copolymer, which is a single type or a combination of polyvinyl alcohol and polyvinyl alcohol, is 0.05 to 15% by weight.
ール、シクロヘキサノール、フェノキシエタノール、ベ
ンジルオキシエタノールの中から選ばれる一種もしくは
二種以上の一価アルコールの配合量が1〜30重量%で
ある請求項1記載の染毛料組成物。3. The compounding amount of (1) one or more monohydric alcohols selected from benzyl alcohol, n-butanol, cyclohexanol, phenoxyethanol and benzyloxyethanol is 1 to 30% by weight. The hair dye composition according to 1.
である請求項1記載の染毛料組成物。4. The compounding amount of (3) acid is 0.1 to 10% by weight.
The hair dye composition according to claim 1, which is
2重量%である請求項1記載の染毛料組成物。5. The compounding amount of (4) acid dye is 0.001 to 0.001.
The hair dye composition according to claim 1, which is 2% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18430896A JP3476623B2 (en) | 1996-05-31 | 1996-05-31 | Hair dye composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18430896A JP3476623B2 (en) | 1996-05-31 | 1996-05-31 | Hair dye composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH09323921A true JPH09323921A (en) | 1997-12-16 |
JP3476623B2 JP3476623B2 (en) | 2003-12-10 |
Family
ID=16151073
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18430896A Expired - Lifetime JP3476623B2 (en) | 1996-05-31 | 1996-05-31 | Hair dye composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3476623B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH10245327A (en) * | 1997-03-03 | 1998-09-14 | Lion Corp | Hair dye composition |
JP2002226335A (en) * | 2001-02-02 | 2002-08-14 | Nonogawa Shoji Kk | Acidic hair dye composition for hair |
-
1996
- 1996-05-31 JP JP18430896A patent/JP3476623B2/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH10245327A (en) * | 1997-03-03 | 1998-09-14 | Lion Corp | Hair dye composition |
JP2002226335A (en) * | 2001-02-02 | 2002-08-14 | Nonogawa Shoji Kk | Acidic hair dye composition for hair |
Also Published As
Publication number | Publication date |
---|---|
JP3476623B2 (en) | 2003-12-10 |
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