JP2617340B2 - Hair dye composition - Google Patents

Hair dye composition

Info

Publication number
JP2617340B2
JP2617340B2 JP19514588A JP19514588A JP2617340B2 JP 2617340 B2 JP2617340 B2 JP 2617340B2 JP 19514588 A JP19514588 A JP 19514588A JP 19514588 A JP19514588 A JP 19514588A JP 2617340 B2 JP2617340 B2 JP 2617340B2
Authority
JP
Japan
Prior art keywords
hair
agent
dye
dyeing
hair dye
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 - Lifetime
Application number
JP19514588A
Other languages
Japanese (ja)
Other versions
JPH02231413A (en
Inventor
光比己 木野
いずみ 末久
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 JP19514588A priority Critical patent/JP2617340B2/en
Publication of JPH02231413A publication Critical patent/JPH02231413A/en
Application granted granted Critical
Publication of JP2617340B2 publication Critical patent/JP2617340B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Cosmetics (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は染毛剤組成物に関するもので、詳しくは、染
め上がりに優れている上、毛髪の損傷が極めて少ない染
毛組成物に関するものである。
Description: TECHNICAL FIELD The present invention relates to a hair dye composition, and more particularly, to a hair dye composition which is excellent in dyeing and has very little damage to hair. .

(従来技術とその問題点) 従来、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、髪の中で酸化重合
を行なわせることにより色素を生成させ毛髪を染着する
ものである。しかしながら、これらの染毛剤は要望に応
じた種々の色調に毛髪を染毛することができ、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
が、染毛処理によって毛髪が損傷し、そのため、毛髪に
潤いおよび光沢がなくな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う欠点がある。
(Prior art and its problems) Conventionally, the first hair dye containing an oxidation dye intermediate was used.
2. Description of the Related Art A two-part type oxidative hair dye consisting of an agent and a second agent containing an oxidizing agent is widely used. This hair coloring agent is a dye that causes a colorless low-molecular weight oxidation dye intermediate to penetrate into the hair and causes oxidative polymerization in the hair to form a pigment to dye the hair. However, these hair dyes can dye hair in various colors as desired, and
It is very convenient because its hair dyeing power is also excellent, but the hair dyeing treatment damages the hair, so the hair loses moisture and luster and the dyeing becomes unnatural color, giving a strange feeling to a third party In addition, there is a disadvantage that the hair is not supple due to poor combing.

そこで、従来、このような欠点を改善するために種々
の配合剤が研究されているが、毛髪の損傷を十分に防止
できる配合剤の場合には、染毛剤として堅牢に染毛力を
発揮するという染毛剤自体の効果を阻害するものが多
く、更に改善が望まれている。
Therefore, various compounding agents have been studied in order to improve such disadvantages, but in the case of a compounding agent capable of sufficiently preventing damage to the hair, the compound exhibits a strong hair dyeing power as a hair dye. In many cases, the effect of the hair dye itself is impaired, and further improvement is desired.

(発明の課題と解決手段) 本発明者は上記実情に鑑み、染毛処理において、毛髪
の染毛力には悪影響を与えず、毛髪の損傷を防止し、染
毛後の毛髪に潤いと光沢があり自然な染め上がりとなる
染毛剤組成物を得ることを目的として鋭意検討した結
果、ある特定の化合物を配合することにより本発明の目
的が達成されることを見出し、本発明を完成するに到っ
た。
(Problems and Solution to the Invention) In view of the above-mentioned circumstances, the present inventor has found that in the hair dyeing treatment, the hair dyeing power is not adversely affected, the hair is prevented from being damaged, and the hair after dyeing is moistened and glossy. As a result of intensive studies with the aim of obtaining a hair dye composition that has a natural dyeing, it has been found that the object of the present invention can be achieved by blending a specific compound, and to complete the present invention. It has arrived.

すなわち、本発明の趣旨は、パラアミノ安息香酸、パ
ラアミノ安息香酸エチル、パラアミノ安息香酸グリセリ
ル、パラアミノ安息香酸イソブチル、パラジメチルアミ
ノ安息香酸アミル、パラジメチルアミノ安息香酸オクチ
ル、パラジメチルアミノ安息香酸イソオクチル、パラジ
エトキシアミノ安息香酸エチル、パラジプロポキシアミ
ノ安息香酸エチルから選ばれた少なくとも一種の化合物
を配合したことを特徴とする染毛剤組成物に存する。
That is, the gist of the present invention is that paraaminobenzoic acid, ethyl paraaminobenzoate, glyceryl paraaminobenzoate, isobutyl paraaminobenzoate, amyl paradimethylaminobenzoate, octyl paradimethylaminobenzoate, isooctyl paradimethylaminobenzoate, paradiethoxy. A hair dye composition comprising at least one compound selected from ethyl aminobenzoate and ethyl paradipropoxyaminobenzoate.

以下、本発明の構成について詳細に説明する。 Hereinafter, the configuration of the present invention will be described in detail.

本発明で対象となる染毛剤は酸化染料中間体を主剤と
する第1剤と酸化剤を主剤とする第2剤からなる酸化染
毛剤である。酸化染料中間体としては、通常、フェニレ
ンジアミン類、アミノフェノール類、トルイレンジアミ
ン類、アミノニトロフェノール類、ジフェニルアミン
類、ジアミノフェニルアミン類、N−フェニルフェニレ
ンジアミン類、ジアミノピリジン類等およびそれらの塩
類の1種または2種以上が挙げられる。その配合量は例
えば、第1剤の全重量に対して0.01〜10重量%程度であ
る。また、カップラーとしてレゾルシン、ピロガロー
ル、カテコール、メタアミノフェノール、メタフェニレ
ンジアミン等を配合することができる。また、「染毛剤
原料規格」(改訂第3版,昭和60年5月発行,日本ヘア
カラー工業会、染毛剤懇話会発行)に収載されたものを
用いることができる。更に、ポリオキシエチレンアルキ
ルエーテル、ポリオキシエチレンアルキルアミン脂肪酸
アミド等の界面活性剤、グリセリン、プロピレングリコ
ール等の保湿剤、ラノリン、スクワラン、流動パラフィ
ン等の油性成分、亜硫酸塩、アスコルビン酸等の安定
剤、カルボキシメチルセルロース等の増粘剤、アンモニ
ア、アルカノールアミン等のアルカリ剤、高級アルコー
ル、香料などを必要に応じて適宜、配合することができ
る。一方、第2剤としては、過酸化水素、過酸化尿素等
の酸化剤を含有し、また、フェナセチン、EDTA等の安定
剤、界面活性剤、油脂類、高級アルコール、酸、pH調整
剤、香料などを必要に応じて適宜、配合することができ
る。この染毛剤を使用する場合は、染毛処理の直前に第
1剤と第2剤を混合して毛髪に塗布する。
The hair dye targeted in the present invention is an oxidative hair dye comprising a first agent mainly containing an oxidation dye intermediate and a second agent mainly containing an oxidant. Examples of the oxidation dye intermediate include phenylenediamines, aminophenols, toluylenediamines, aminonitrophenols, diphenylamines, diaminophenylamines, N-phenylphenylenediamines, diaminopyridines, and salts thereof. Or one or more of these. The compounding amount is, for example, about 0.01 to 10% by weight based on the total weight of the first agent. In addition, resorcin, pyrogallol, catechol, metaaminophenol, metaphenylenediamine and the like can be blended as a coupler. Further, those described in "Hair Coloring Material Standards" (Revised 3rd Edition, published in May 1985, published by Japan Hair Color Industry Association and Hair Dyeing Society) can be used. Furthermore, surfactants such as polyoxyethylene alkyl ether and polyoxyethylene alkylamine fatty acid amide; humectants such as glycerin and propylene glycol; oily components such as lanolin, squalane and liquid paraffin; stabilizers such as sulfites and ascorbic acid. , A thickening agent such as carboxymethylcellulose, an alkali agent such as ammonia or alkanolamine, a higher alcohol, a fragrance and the like can be appropriately compounded as required. On the other hand, the second agent contains an oxidizing agent such as hydrogen peroxide, urea peroxide, etc., and also includes stabilizers such as phenacetin and EDTA, surfactants, fats and oils, higher alcohols, acids, pH adjusters, and fragrances. And the like can be appropriately compounded as needed. When this hair dye is used, the first and second agents are mixed and applied to the hair immediately before the hair dyeing treatment.

本発明は上記染毛剤にパラアミノ安息香酸、パラアミ
ノ安息香酸エチル、パラアミノ安息香酸グリセリル、パ
ラアミノ安息香酸イソブチル、パラジメチルアミノ安息
香酸アミル、パラジメチルアミノ安息香酸オクチル、パ
ラジメチルアミノ安息香酸イソオクチル、パラジエトキ
シアミノ安息香酸エチル、パラジプロポキシアミノ安息
香酸エチルから選ばれた少なくとも一種の化合物を配合
することを必須の要件とするものである。すなわち、こ
れらの化合物の配合により、毛髪の損傷を防止しながら
染毛処理ができ、しかも堅牢な色調を得ることができ
る。これらの化合物の配合量は染毛剤全量に対して通
常、0.01〜10重量%、好ましくは0.05〜5重量%であ
る。この配合量が0.01重量%未満の場合には、毛髪の損
傷を十分に防止し、潤いと光沢のある毛髪を得ることが
難しく、逆に10重量%より多くても、効果に大きな差異
はなく経済的でない。
The present invention relates to the above hair dye, wherein para-aminobenzoic acid, ethyl para-aminobenzoate, glyceryl para-aminobenzoate, isobutyl para-aminobenzoate, amyl para-dimethyl amino benzoate, octyl para-dimethyl amino benzoate, iso-octyl para-dimethyl amino benzoate, para-diethoxy. It is an essential requirement that at least one compound selected from ethyl aminobenzoate and ethyl paradipropoxyaminobenzoate be blended. That is, by compounding these compounds, hair dyeing treatment can be performed while preventing damage to the hair, and a robust color tone can be obtained. The compounding amount of these compounds is usually 0.01 to 10% by weight, preferably 0.05 to 5% by weight based on the total amount of the hair dye. If the amount is less than 0.01% by weight, it is difficult to sufficiently prevent hair damage, and it is difficult to obtain moist and shiny hair. Conversely, if the amount is more than 10% by weight, there is no significant difference in the effect. Not economic.

(実施例) 次に、本発明を実施例により更に具体的に説明する
が、本発明はその要旨を越えないかぎり、以下の実施例
に限定されるものではない。
(Examples) Next, the present invention will be described more specifically with reference to examples, but the present invention is not limited to the following examples unless it exceeds the gist.

実施例1 第1剤 p−フェニレンジアミン 1.0% プロピレングリコール 10.0% EDTA−Na 0.3% 亜硫酸ナトリウム 0.5% パラアミノ安息香酸 0.1% アンモニア pH10.0になる量 精製水で100%にする。Example 1 First agent p-phenylenediamine 1.0% propylene glycol 10.0% EDTA-Na 0.3% sodium sulfite 0.5% para-aminobenzoic acid 0.1% ammonia Amount to become pH 10.0 Make 100% with purified water.

第2剤 過酸化水素 6.0% 精製水で100%にする。Second agent Hydrogen peroxide 6.0% Make 100% with purified water.

上記組成の本発明の染毛剤を調製し第1剤と第2剤と
を1:1で混合し、これを室温にてパネラー(A〜Eの5
名)の頭髪半分に塗布するとともに、比較のために、上
記染毛剤よりパラアミノ安息香酸を除外した同様の染毛
剤を対照として同パネラーの残りの半分の頭髪に同条件
で塗布した。
The hair dye of the present invention having the above composition was prepared, the first agent and the second agent were mixed at a ratio of 1: 1, and this was mixed at room temperature with panelists (A to E 5).
) Was applied to the other half of the hair of the same panel as a control, with the same hair dye except that paraaminobenzoic acid was omitted from the above hair dye for comparison.

そして、両染毛剤を塗布後、20分間放置した後、各パ
ネラーの頭髪を40℃の温湯で十分すすぎ、次いで、乾燥
した。このような染毛処理を終えた各パネラーの頭髪に
関して、対照例に対する実施例の染め上がり、毛髪の仕
上り、毛髪の損傷について下記の基準で行なったところ
第1表に示す結果を得た。
Then, after both hair dyes were applied, the hair was left for 20 minutes, and then the hair of each panelist was sufficiently rinsed with warm water at 40 ° C., and then dried. With respect to the hair of each paneler after the hair dyeing treatment, dyeing, finishing of the hair, and damage to the hair of the example with respect to the control example were performed according to the following criteria, and the results shown in Table 1 were obtained.

<評価基準> (1)染め上がり ○:実施例の方が対照例と比較して光沢のある染め上が
りで、その光沢が持続する。
<Evaluation Criteria> (1) Dyeing ○: The example is a glossy dyeing as compared with the control example, and the gloss is maintained.

△:実施例と対照例の染め上がりは同程度 ×:実施例の方が対照例と比較して光沢に欠ける染め上
がり (2)毛髪の仕上り ○:実施例の方が対照例と比較してしなやかで櫛通りが
よい △:実施例と対照例のしなやかさ、櫛通りは同程度 ×:実施例の方が対照例と比較してしなやかさがなく、
櫛通りが劣る (3)毛髪の損傷 毛髪の表面を電子顕微鏡(倍率3000倍)で観察し、毛
小皮の損傷の程度を評価した。
Δ: Dyeing of the example and the control was comparable. ×: Dyeing of the example lacking in gloss compared to the control. (2) Finishing of hair ○: The example was more supple than the control. Good combability Δ: flexibility of Example and control example, comparable degree of combability ×: less flexibility in Example than in Comparative Example,
Poor combability (3) Damage to hair The surface of the hair was observed with an electron microscope (3000 times magnification) to evaluate the degree of damage to the hair dermal.

○:実施例の方が対照例と比較して損傷が少ない △:実施例と対照例の損傷は同程度 ×:実施例の方が対照例と比較して損傷が多い 実施例2 第1剤 p−フェニレンジアミン 1.0% プロピレングリコール 10.0% EDTA−Na 0.3% 亜硫酸ナトリウム 0.5% パラアミノ安息香酸エチル 0.2% アンモニア pH10.0になる量 精製水で100%にする。:: Example has less damage as compared to control example Δ: Example and control example have similar damage ×: Example has more damage than control example Example 2 First agent p-phenylenediamine 1.0% propylene glycol 10.0% EDTA-Na 0.3% sodium sulfite 0.5% ethyl paraaminobenzoate 0.2% ammonia Amount to reach pH 10.0 Make up to 100% with purified water.

第2剤 過酸化水素 6.0% 精製水で100%にする。Second agent Hydrogen peroxide 6.0% Make 100% with purified water.

上記組成の本発明の染毛剤を調製し第1剤と第2剤と
を1:1で混合し、これを室温にてパネラー(F〜Jの5
名)の頭髪半分に塗布するとともに、比較のために、上
記染毛剤よりパラアミノ安息香酸エチルを除外した同様
の染毛剤を対照例として同パネラーの残りの半分の頭髪
に同条件で塗布した。
The hair dye of the present invention having the above composition was prepared, and the first and second agents were mixed at a ratio of 1: 1.
Name), and for comparison, a similar hair dye except that ethyl paraaminobenzoate was omitted from the above hair dye as a control was applied to the other half of the hair of the same paneler under the same conditions. .

そして、両染毛剤を塗布後、20分間放置した後、各パ
ネラーの頭髪を40℃の温湯で十分すすぎ、次いで、乾燥
した。このような染毛処理を終えた各パネラーの頭髪に
関して、実施例1と同様な評価を行なったところ第2表
に示す結果を得た。
Then, after both hair dyes were applied, the hair was left for 20 minutes, and then the hair of each panelist was sufficiently rinsed with warm water at 40 ° C., and then dried. The same evaluation as in Example 1 was performed on the hair of each paneler after the hair dyeing treatment, and the results shown in Table 2 were obtained.

実施例3 第1剤 第2剤 上記組成のクリーム状の染毛剤の第1剤と第2剤を1:
1で混合し白髪に塗布し、常温で20分間放置した後、シ
ャンプーを用いて洗髪した。その結果、実施例1〜2と
同様に染め上がりに優れ、毛髪の仕上りのよい堅牢な黒
褐色に染毛された。
Example 3 First Agent 2nd agent The first and second cream hair dyes of the above composition are:
The mixture was mixed in 1 and applied to gray hair, left at room temperature for 20 minutes, and then washed with shampoo. As a result, as in Examples 1 and 2, the dye was excellent in dyeing, and the hair was dyed into a strong blackish brown with good finish.

実施例4 第1剤 第2剤 上記組成のゲル状の染毛剤の第1剤と第2剤を1:1で
混合し白髪に塗布し、常温で20分間放置した後、シャン
プーを用いて洗髪した。その結果、実施例1〜2と同様
に染め上がりに優れ、毛髪の仕上りのよい堅牢な黒色に
染毛された。
Example 4 First Agent 2nd agent The first and second gelled hair dyes having the above composition were mixed at a ratio of 1: 1 and applied to white hair. After standing at room temperature for 20 minutes, the hair was washed with a shampoo. As a result, as in Examples 1 and 2, the dye was excellent in dyeing, and the hair was dyed into a strong black with good finish.

実施例5〜8 実施例3において、第1剤の組成中、パラアミノ安息
香酸グリセリル1.0%の代わりに、第3表に示す同量の
本発明の化合物を配合し、その他は実施例3と全く同様
な方法で染毛処理したところ、いずれも、毛髪の損傷が
なく、染め上がりに優れた堅牢な染毛ができた。
Examples 5 to 8 In Example 3, the same amount of the compound of the present invention shown in Table 3 was blended in place of glyceryl paraaminobenzoate 1.0% in the composition of the first agent, and the others were completely the same as Example 3. When the hair was dyed in the same manner, no hair was damaged, and a robust hair dyeing excellent in dyeing was obtained.

(発明の効果) 本発明の染毛剤組成物によれば、染毛剤としての染着
効果を損なうことなく、毛髪の損傷防止ができ、その結
果、潤いと光沢のある自然な色の毛髪を得ることができ
る上、櫛通りもよいとの優れた効果を有する。また、堅
牢性にも優れており、特に日光堅牢性が優れている。
(Effect of the Invention) According to the hair dye composition of the present invention, it is possible to prevent damage to the hair without impairing the dyeing effect as a hair dye, and as a result, moist and shiny natural color hair Can be obtained, and it has an excellent effect that combing is good. In addition, it has excellent fastness, particularly excellent fastness to sunlight.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】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剤からなる酸化染毛剤において、どちら
か一方または両方にパラアミノ安息香酸、パラアミノ安
息香酸エチル、パラアミノ安息香酸グリセリル、パラア
ミノ安息香酸イソブチル、パラジメチルアミノ安息香酸
アミル、パラジメチルアミノ安息香酸オクチル、パラジ
メチルアミノ安息香酸イソオクチル、パラジエトキシア
ミノ安息香酸エチル、パラジプロポキシアミノ安息香酸
エチルから選ばれる1種または2種以上を含むことを特
徴とする染毛剤組成物。
An oxidative hair dye comprising a first agent containing an intermediate of an oxidative dye and a second agent containing an oxidizing agent, wherein at least one or both of them comprises para-aminobenzoic acid, ethyl para-aminobenzoate, and para-aminobenzoic acid. One or more selected from glyceryl, isobutyl paraaminobenzoate, amyl paradimethylaminobenzoate, octyl paradimethylaminobenzoate, isooctyl paradimethylaminobenzoate, ethyl paradiethoxyaminobenzoate, ethyl paradipropoxyaminobenzoate A hair dye composition comprising:
JP19514588A 1988-08-04 1988-08-04 Hair dye composition Expired - Lifetime JP2617340B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19514588A JP2617340B2 (en) 1988-08-04 1988-08-04 Hair dye composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19514588A JP2617340B2 (en) 1988-08-04 1988-08-04 Hair dye composition

Publications (2)

Publication Number Publication Date
JPH02231413A JPH02231413A (en) 1990-09-13
JP2617340B2 true JP2617340B2 (en) 1997-06-04

Family

ID=16336188

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19514588A Expired - Lifetime JP2617340B2 (en) 1988-08-04 1988-08-04 Hair dye composition

Country Status (1)

Country Link
JP (1) JP2617340B2 (en)

Also Published As

Publication number Publication date
JPH02231413A (en) 1990-09-13

Similar Documents

Publication Publication Date Title
JP2003238370A (en) Hair dye composition
JP2659740B2 (en) Hair dye composition
JPH07330559A (en) Hairdye composition
JP2951124B2 (en) Hair dye composition
JP3345174B2 (en) Hair treatment agent
JP2000264822A (en) Hair dye composition
JP2872385B2 (en) Hair dye
JP2617340B2 (en) Hair dye composition
JPH092923A (en) Hair-dyeing agent
JP2000336020A (en) Hair dye composition
JP4311785B2 (en) Hair dye composition containing 3-methyl-aminophenol and 2-methyl-1-naphthol
JP2950746B2 (en) Powder hair dye composition
JP3441785B2 (en) Hair dye composition
JPH078777B2 (en) Hair dye composition
JP2779183B2 (en) Hair dye composition
JPH0432046B2 (en)
JP2726272B2 (en) Hair dye composition
JPH1160454A (en) Composition for hair dyeing
JPH09315944A (en) Hair-treating agent composition
JP3446977B2 (en) Hair dye
JP3113414B2 (en) Hair dye composition
JPH082775B2 (en) Hair dye composition
JPH0720853B2 (en) Hair dye composition
KR0163530B1 (en) Hair dye compositions
JPH08301738A (en) Hair dyeing agent composition