JPH10182371A - Hair dyeing agent - Google Patents

Hair dyeing agent

Info

Publication number
JPH10182371A
JPH10182371A JP35489396A JP35489396A JPH10182371A JP H10182371 A JPH10182371 A JP H10182371A JP 35489396 A JP35489396 A JP 35489396A JP 35489396 A JP35489396 A JP 35489396A JP H10182371 A JPH10182371 A JP H10182371A
Authority
JP
Japan
Prior art keywords
hair
dyeing
protein hydrolyzate
dye
comparative example
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.)
Pending
Application number
JP35489396A
Other languages
Japanese (ja)
Inventor
Masato Yoshioka
正人 吉岡
Masakazu Kitayama
雅一 北山
Koji Nosaka
浩司 野坂
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.)
Seiwa Kasei Co Ltd
Original Assignee
Seiwa Kasei 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 Seiwa Kasei Co Ltd filed Critical Seiwa Kasei Co Ltd
Priority to JP35489396A priority Critical patent/JPH10182371A/en
Publication of JPH10182371A publication Critical patent/JPH10182371A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide a hair dyeing agent quick in starting of hair dyeing, capable of uniformly dyeing hair, excellent in shampoo resistance of hair after dyeing, slightly damaging hair during hair dyeing, capable of providing hair with luster and moisture. SOLUTION: This oxidation type hair dyeing agent contains one or more of a protein hydrolyzate derived from an animal and a plant and/or a microorganism and its derivative. A hydrolyzed keratin and a hydrolyzed collagen are preferable as the protein hydrolyzate. A quaternary ammonium derivative of the protein hydrolyzate and an acylated protein hydrolyzate or its salt are preferable as the protein hydrolyzate derivative.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、染毛剤に関し、さ
らに詳しくは、酸化型染毛剤に属する染毛剤であって、
染毛の立ち上がりが速く、均一に染毛でき、しかも染毛
後の毛髪の耐シャンプー性が優れ、かつ染毛時の毛髪の
損傷が少なく、染毛後の毛髪に艶や潤いを付与すること
ができる染毛剤に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a hair dye, and more particularly, to a hair dye belonging to an oxidative hair dye,
Fast hair rise, uniform hair dyeing, excellent hair shampoo resistance after hair dyeing, less damage to hair at the time of hair dyeing, giving gloss and moisture to hair after hair dyeing The present invention relates to a hair dye that can be used.

【0002】[0002]

【従来の技術】染毛剤には、一時染毛剤、半永久染毛
剤、永久染毛剤などがあり、いずれも美容の目的で広く
使用されている。
2. Description of the Related Art Hair dyes include temporary hair dyes, semi-permanent hair dyes and permanent hair dyes, all of which are widely used for cosmetic purposes.

【0003】このうち永久染毛剤では、酸化染料(染料
中間体)を含む第1剤と過酸化水素などの酸化剤を含む
第2剤とからなる酸化型染毛剤が、種々の色調が得られ
る上に、染毛力が優れていることから、広く使用されて
いる。
Among the permanent hair dyes, oxidized hair dyes composed of a first agent containing an oxidation dye (dye intermediate) and a second agent containing an oxidizing agent such as hydrogen peroxide have various colors. It is widely used because it is obtained and has excellent hair dyeing power.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、酸化型
染毛剤では、酸化染料を含む第1剤と酸化剤を含む第2
剤を使用前に混合して頭髪に塗布するため、酸性染料を
主成分とする酸性染毛料に比べて毛髪上での発色に時間
がかかる上に、均一に染まりにくいという問題がある。
However, in the case of an oxidative hair dye, a first agent containing an oxidizing dye and a second agent containing an oxidizing agent are used.
Since the agent is mixed before use and applied to the hair, there is a problem in that it takes more time to develop color on the hair than in the case of an acid hair dye containing an acid dye as a main component, and it is difficult to uniformly dye the hair.

【0005】また、酸化型染毛剤では、一般に酸化染料
の均一な浸透を助長するためにアルカリ剤を含有させて
いるので、pHが10以上と高く、そのため、刺激性が
あり、かつ毛髪中のタンパク(蛋白)成分が流出しやす
く、染毛時の毛髪の損傷が激しいので、染毛後の毛髪が
パサついたり、櫛通り性が悪くなるという問題もあっ
た。
[0005] Oxidative hair dyes generally contain an alkaline agent to promote uniform penetration of the oxidative dye, so that the pH is as high as 10 or more, which is irritating and causes hair to irritate. The protein (protein) component easily leaks out, and the hair is severely damaged at the time of hair dyeing.

【0006】従って、本発明は、染毛の立ち上がりが速
く、均一に染毛でき、しかも染毛後の毛髪の耐シャンプ
ー性が優れ、かつ染毛時の毛髪の損傷が少なく、染毛後
の毛髪に艶、潤いを付与することができる染毛剤を提供
することを目的とする。
Accordingly, the present invention provides a hair dye which has a fast rise time, can be uniformly dyed, has excellent shampoo resistance of the hair after dyeing, and has little damage to the hair at the time of hair dyeing. An object of the present invention is to provide a hair dye capable of imparting gloss and moisture to hair.

【0007】[0007]

【課題を解決するための手段】本発明者らは、上記課題
を解決するため鋭意研究を重ねた結果、動植物および/
または微生物由来の蛋白質加水分解物またはその誘導体
の1種以上を酸化型染毛剤に含有させるときは、染毛の
立ち上がりが速く、均一に染毛でき、しかも染毛後の耐
シャンプー性が優れ、かつ染毛時の毛髪の損傷が少な
く、染毛後の毛髪に艶や潤い、良好な櫛通り性などを付
与できることを見出し、本発明を完成するにいたった。
Means for Solving the Problems The present inventors have made intensive studies to solve the above-mentioned problems, and as a result, have found that animals and plants and / or
Alternatively, when one or more of a microorganism-derived protein hydrolyzate or a derivative thereof is contained in the oxidized hair dye, the hair dyes rise rapidly, can be uniformly dyed, and have excellent shampoo resistance after hair dyeing. The present inventors have found that hair damage during hair dyeing is small, and that the hair after hair dyeing can impart luster, moisture, and good combability to complete the present invention.

【0008】すなわち、毛髪には傷んだ部分と健常な部
分とがあり、これが染毛剤の毛髪への浸透に相違を生じ
させ、染毛時の染毛速度の違いおよび色むらを引き起こ
す原因の一つになると言われているが、本発明の染毛剤
では、動植物および/または微生物由来の蛋白質加水分
解物またはその誘導体が毛髪の損傷部を保護すると共に
健常部分も含めて均一な被膜を形成するので、染毛剤の
浸透に相違が生じず、かつ染毛剤の発色速度が均一にな
り、染毛の度合いも均一になって、色むらの発生が防止
される。
[0008] That is, the hair has a damaged part and a healthy part, and this causes a difference in the penetration of the hair dye into the hair, which causes a difference in the hair dyeing speed at the time of hair dyeing and uneven color. In the hair dye of the present invention, it is said that the protein hydrolyzate or its derivative derived from animals and plants and / or microorganisms protects the damaged part of the hair and forms a uniform film including the healthy part. Since it is formed, there is no difference in the penetration of the hair dye, the coloring speed of the hair dye becomes uniform, the degree of hair dyeing becomes uniform, and the occurrence of color unevenness is prevented.

【0009】さらに、本発明の染毛剤では、動植物およ
び/または微生物由来の蛋白質加水分解物またはその誘
導体が毛髪に収着して毛髪を保護するので、染毛剤中に
含まれるアルカリ剤や酸化剤による毛髪の損傷が防止さ
れると共に、染毛後の毛髪に艶や潤い、良好な櫛通り性
などが付与される。
Furthermore, in the hair dye of the present invention, since a protein hydrolyzate or a derivative thereof derived from animals and plants and / or microorganisms sorbs to the hair to protect the hair, the alkaline agent contained in the hair dye and In addition to preventing the hair from being damaged by the oxidizing agent, the hair after dyeing is imparted with luster, moisture and good combability.

【0010】[0010]

【発明の実施の形態】本発明において、染毛剤に含有さ
せる動植物および/または微生物由来の蛋白質加水分解
物としては、たとえば、コラーゲン(その変成物である
ゼラチンも含む)、ケラチン、絹フィブロイン、セリシ
ン、カゼイン、コンキオリン、エラスチン、鶏、あひる
などの卵の卵黄タンパク、卵白タンパク、大豆タンパ
ク、小麦タンパク、トウモロコシタンパク、米(米糠)
タンパク、ジャガイモタンパクなどの動植物由来のタン
パク、または、サッカロミセス属、カンディタ属、エン
ドミコプシス属の酵母菌や、いわゆるビール酵母、清酒
酵母といわれる酵母菌より分離した酵母タンパク、キノ
コ類(担子菌)より抽出したタンパク、クロレラより分
離したタンパクなどの微生物由来のタンパクを酸、アル
カリ、酵素またはその併用で部分的に加水分解して得ら
れるペプチドなどが挙げられる。そして、これらの蛋白
質加水分解物は単独で用いてもよいし、また2種以上を
併用してもよい。
BEST MODE FOR CARRYING OUT THE INVENTION In the present invention, the protein hydrolyzate derived from animals, plants and / or microorganisms to be contained in the hair dye includes, for example, collagen (including gelatin which is a denatured product thereof), keratin, silk fibroin, Egg yolk protein, egg white protein, soy protein, wheat protein, corn protein, rice (rice bran) of eggs such as sericin, casein, conchiolin, elastin, chicken and duck
Proteins derived from animals and plants such as proteins and potato proteins, or yeasts of the genera Saccharomyces, Candita and Endomycopsis, and yeast proteins and mushrooms (basidiomycetes) isolated from yeasts called beer yeasts and sake yeasts Peptides obtained by partially hydrolyzing proteins derived from microorganisms such as extracted proteins and proteins isolated from Chlorella with acids, alkalis, enzymes or a combination thereof. These protein hydrolysates may be used alone or in combination of two or more.

【0011】この蛋白質加水分解物は、毛髪への収着性
および造膜作用の点を考慮して、数平均分子量が150
〜5000のものが好ましく、特に200〜3000の
ものが好ましい。すなわち、蛋白質加水分解物の数平均
分子量が150より小さい場合は、毛髪への浸透作用は
優れているものの、毛髪上での造膜作用に乏しく、また
数平均分子量が5000より大きい場合は、造膜作用は
強いものの、毛髪への浸透作用が弱くなり、毛髪の損傷
部の保護・回復作用が充分に発揮されなくなるおそれが
ある。
The protein hydrolyzate has a number average molecular weight of 150 in consideration of the sorption property to hair and the effect of forming a film.
5,000 are preferable, and 200-3000 are particularly preferable. That is, when the number average molecular weight of the protein hydrolyzate is smaller than 150, the effect of penetrating the hair is excellent, but the film forming action on the hair is poor, and when the number average molecular weight is larger than 5000, the film forming action is Although strong, the effect of penetrating the hair is weakened, and the effect of protecting and recovering damaged hair parts may not be sufficiently exhibited.

【0012】上記動植物および/または微生物由来の蛋
白質加水分解物の誘導体としては、上記蛋白質加水分解
物のエステル、第4級アンモニウム誘導体、アシル化物
またはその塩などが挙げられる。
The derivatives of the protein hydrolyzate derived from animals and plants and / or microorganisms include esters, quaternary ammonium derivatives, acylated products and salts thereof of the protein hydrolyzate.

【0013】上記蛋白質加水分解物のエステルとして
は、上記蛋白質加水分解物のカルボキシル基における炭
素数1〜20の炭化水素アルコールとのエステル、たと
えば、メチルエステル、エチルエステル、プロピルエス
テル、イソプロピルエステル、ラウリルエステル、セチ
ルエステル、2−エチルヘキシルエステル、2−ヘキシ
ルデシルエステル、ステアリルエステルなどが挙げられ
る。
The ester of the protein hydrolyzate may be an ester with a hydrocarbon alcohol having 1 to 20 carbon atoms at the carboxyl group of the protein hydrolyzate, for example, methyl ester, ethyl ester, propyl ester, isopropyl ester, lauryl. Esters, cetyl esters, 2-ethylhexyl esters, 2-hexyldecyl esters, stearyl esters and the like can be mentioned.

【0014】上記蛋白質加水分解物の第4級アンモニウ
ム誘導体としては、たとえば、上記蛋白質加水分解物の
アミノ基に下記一般式(I)
Examples of the quaternary ammonium derivative of the protein hydrolyzate include the following general formula (I):

【0015】[0015]

【化1】 Embedded image

【0016】〔式中、R1 、R2 、R3 は炭素数1〜3
のアルキル基もしくはヒドロキシアルキル基、またはR
1 〜R2 のうち1個もしくは2個が炭素数8〜20のア
ルキル基もしくはアルケニル基で、残りは炭素数1〜3
のアルキル基、炭素数1〜3のヒドロキシアルキル基も
しくはベンジル基であり、XはCl、Br、F、I、N
3 、1/2SO4 、R4 OSO3 またはR4 SO
3 (R4 は低級アルキル基を示す)を示す〕で表される
グリシジルアンモニウム塩、または下記一般式(II)
Wherein R 1 , R 2 and R 3 each have 1 to 3 carbon atoms.
An alkyl group or a hydroxyalkyl group of
One or two of R 1 to R 2 are an alkyl group or an alkenyl group having 8 to 20 carbon atoms, and the rest are 1 to 3 carbon atoms.
X is a hydroxyalkyl group or a benzyl group having 1 to 3 carbon atoms, and X is Cl, Br, F, I, N
O 3 , SOSO 4 , R 4 OSO 3 or R 4 SO
3 (R 4 represents a lower alkyl group)] or a glycidyl ammonium salt represented by the following general formula (II)

【0017】[0017]

【化2】 Embedded image

【0018】〔式中、R1 、R2 、R3 は炭素数1〜3
のアルキル基もしくはヒドロキシアルキル基、またはR
1 〜R2 のうち1個もしくは2個が炭素数8〜20のア
ルキル基もしくはアルケニル基で、残りは炭素数1〜3
のアルキル基、炭素数1〜3のヒドロキシアルキル基も
しくはベンジル基であり、XはCl、Br、F、I、N
3 、1/2SO4 、R4 OSO3 またはR4 SO
3 (R4 は低級アルキル基を示す)を示し、YはCl、
Br、F、Iなどのハロゲン原子を示す〕で表される3
−ハロゲン−2−ヒドロキシプロピルアンモニウム塩、
または一般式(III)
Wherein R 1 , R 2 and R 3 each have 1 to 3 carbon atoms.
An alkyl group or a hydroxyalkyl group of
One or two of R 1 to R 2 are an alkyl group or an alkenyl group having 8 to 20 carbon atoms, and the rest are 1 to 3 carbon atoms.
X is a hydroxyalkyl group or a benzyl group having 1 to 3 carbon atoms, and X is Cl, Br, F, I, N
O 3 , SOSO 4 , R 4 OSO 3 or R 4 SO
3 (R 4 represents a lower alkyl group), Y is Cl,
Represents a halogen atom such as Br, F, I, etc.]
-Halogen-2-hydroxypropyl ammonium salt,
Or the general formula (III)

【0019】[0019]

【化3】 Embedded image

【0020】〔式中、R1 、R2 、R3 は炭素数1〜3
のアルキル基もしくはヒドロキシアルキル基、またはR
1 〜R2 のうち1個もしくは2個が炭素数8〜20のア
ルキル基もしくはアルケニル基で、残りは炭素数1〜3
のアルキル基、炭素数1〜3のヒドロキシアルキル基も
しくはベンジル基であり、XはCl、Br、F、I、N
3 、1/2SO4 、R4 OSO3 またはR4 SO
3 (R4 は低級アルキル基を示す)を示し、YはCl、
Br、F、Iなどのハロゲン原子を示す〕で表される3
−ハロゲン−プロピルアンモニウム塩のいずれかを反応
させることによって得られたものが挙げられる。
Wherein R 1 , R 2 and R 3 each have 1 to 3 carbon atoms.
An alkyl group or a hydroxyalkyl group of
One or two of R 1 to R 2 are an alkyl group or an alkenyl group having 8 to 20 carbon atoms, and the rest are 1 to 3 carbon atoms.
X is a hydroxyalkyl group or a benzyl group having 1 to 3 carbon atoms, and X is Cl, Br, F, I, N
O 3 , SOSO 4 , R 4 OSO 3 or R 4 SO
3 (R 4 represents a lower alkyl group), Y is Cl,
Represents a halogen atom such as Br, F, I, etc.]
Those obtained by reacting any one of -halogen-propylammonium salts.

【0021】上記蛋白質加水分解物のアシル化物または
その塩としては、たとえば、上記蛋白質加水分解物のア
ミノ基に炭素数7〜21のアルキル基または炭素数7〜
21のアルケニル基(上記アルキル基やアルケニル基は
直鎖状のものでもよいし、また分岐鎖状のものでもよ
い)を有する高級脂肪酸、または樹脂酸などの脂環構造
の酸を縮合させたものまたはその塩が挙げられる。
As the acylated product of the protein hydrolyzate or a salt thereof, for example, the amino group of the protein hydrolyzate may be an alkyl group having 7 to 21 carbon atoms or a 7 to 21 carbon atom.
A higher fatty acid having an alkenyl group of 21 (the above alkyl group or alkenyl group may be linear or branched), or a product obtained by condensing an acid having an alicyclic structure such as a resin acid. Or a salt thereof.

【0022】それらの酸の具体例としては、たとえば、
カプリル酸、カプリン酸、ラウリル酸、ミリスチン酸、
パルミチン酸、ステアリン酸、アラキン酸、ベヘニン
酸、イソパルミチン酸、イソステアリン酸、ウンデシレ
ン酸、オレイン酸、ミリストレイン酸、エライジン酸、
エルカ酸、リノール酸、リノレン酸、アラキドン酸、ヤ
シ油脂肪酸、牛脂肪酸、樹脂酸(アビエチン酸)などが
挙げられる。
Specific examples of these acids include, for example,
Caprylic acid, capric acid, lauric acid, myristic acid,
Palmitic acid, stearic acid, arachinic acid, behenic acid, isopalmitic acid, isostearic acid, undecylenic acid, oleic acid, myristoleic acid, elaidic acid,
Examples include erucic acid, linoleic acid, linolenic acid, arachidonic acid, coconut oil fatty acids, bovine fatty acids, and resin acids (abietic acid).

【0023】そして蛋白質加水分解物をアシル化する一
般的な方法としては、ショッテン−バウマン(Scho
tten−Baumann)反応を挙げることができ
る。
As a general method for acylating a protein hydrolyzate, Schotten-Baumann (Scho
(ten-Baumann) reaction.

【0024】この反応は、蛋白質加水分解物の水溶液
に、縮合させる高級脂肪酸の酸クロライド誘導体をpH
8〜10のアルカリ条件下で攪拌しながら加える反応で
あり、反応終了後、反応物を塩酸、硫酸などの強酸の水
溶液に放出して遊離物を浮遊沈殿として採取し、これを
水洗して精製した後、遊離のまま、あるいはナトリウ
ム、カリウムなどのアルカリ金属、アンモニウムまたは
モノエタノールアミン、トリエタノールアミン、2−ア
ミノ−2−メチルプロパンジオールなどの有機アミンで
中和して塩の形とし、水またはアルコール、プロピレン
グリコール、流動パラフィン、高級脂肪酸、脂肪酸エス
テルなどの溶剤に溶かして溶液状とするか、あるいは乾
燥して粉末状にして得ることができる。
This reaction is carried out by adding an acid chloride derivative of a higher fatty acid to be condensed to an aqueous solution of a protein hydrolyzate to pH.
This is a reaction to be added while stirring under alkaline conditions of 8 to 10. After completion of the reaction, the reaction product is released into an aqueous solution of a strong acid such as hydrochloric acid or sulfuric acid, and the free substance is collected as a floating precipitate, which is washed with water and purified. And then leave it free or neutralize it with an alkali metal such as sodium or potassium, ammonium or an organic amine such as monoethanolamine, triethanolamine or 2-amino-2-methylpropanediol to form a salt. Alternatively, it can be obtained by dissolving in a solvent such as alcohol, propylene glycol, liquid paraffin, higher fatty acid, or fatty acid ester to form a solution, or by drying to obtain a powder.

【0025】上記動植物および/または微生物由来の蛋
白質加水分解物やその誘導体はいずれも染毛剤に含有さ
せると、染毛の立ち上がりを速くさせ、毛髪を均一に染
毛し、染毛後の毛髪の耐シャンプー性を向上させる。さ
らに、上記蛋白質加水分解物やその誘導体は染毛時の毛
髪の損傷を少なくし、染毛後の毛髪に艶や潤いを付与す
るが、それらの中でも、特に加水分解ケラチン、加水分
解コラーゲンなどが好ましく、とりわけ、それらの第4
級アンモニウム誘導体やアシル化物またはその塩などは
効果が優れている。
When any of the above-mentioned animal and plant and / or microorganism-derived protein hydrolysates and derivatives thereof is contained in a hair dye, the hair dye can be rapidly raised, the hair can be uniformly dyed, and the hair after dyeing can be obtained. Improve the shampoo resistance. Furthermore, the above-mentioned protein hydrolyzate and its derivative reduce the damage of hair at the time of hair dyeing and impart gloss and moisture to the hair after hair dyeing. Among them, hydrolyzed keratin, hydrolyzed collagen and the like are particularly preferable. Preferred, and especially, their fourth
A quaternary ammonium derivative, an acylated compound or a salt thereof is excellent in effect.

【0026】上記動植物および/または微生物由来の蛋
白質加水分解物やその誘導体は、それぞれ単独で用いて
もよいし、また2種以上を混合して用いてもよい。そし
て、動植物および/または微生物由来の蛋白質加水分解
物またはその誘導体の染毛剤中での含有量(染毛剤中へ
の配合量)としては、0.1〜20重量%、特に0.5
〜10重量%の範囲にするのが好ましい。すなわち、上
記蛋白質加水分解物またはその誘導体の染毛剤中での含
有量が上記範囲より少ない場合は、毛髪の損傷部位を保
護して毛髪上で造膜する効果が乏しく、従って染毛時の
染料の均一な浸透や付着が少なくなって、毛髪を均一に
染毛することができなくなるおそれがあり、また上記蛋
白質加水分解物またはその誘導体の染毛剤中での含有量
が上記範囲より多くなっても、増加に見合う効果の増加
がほとんど認められない。
The above-mentioned protein hydrolysates derived from animals and plants and / or microorganisms and derivatives thereof may be used alone or in combination of two or more. The content of the protein hydrolyzate derived from animals and plants and / or microorganisms or a derivative thereof in the hair dye (blending amount in the hair dye) is 0.1 to 20% by weight, particularly 0.5% by weight.
It is preferably in the range of 10 to 10% by weight. That is, when the content of the protein hydrolyzate or a derivative thereof in the hair coloring agent is less than the above range, the effect of protecting the damaged part of the hair and forming a film on the hair is poor, and thus, during hair dyeing. There is a possibility that the uniform penetration and adhesion of the dye may be reduced and the hair may not be dyed uniformly, and the content of the protein hydrolyzate or a derivative thereof in the hair dye is more than the above range. Even so, there is almost no increase in the effect commensurate with the increase.

【0027】本発明の染毛剤において、動植物および/
または微生物由来の蛋白質加水分解物またはその誘導体
以外の成分は、染毛剤に使用可能なものであれば、いず
れも使用することができる。
In the hair dye of the present invention, animals and plants and / or
Alternatively, any component other than the microorganism-derived protein hydrolyzate or derivative thereof can be used as long as it can be used for a hair dye.

【0028】上記動植物および/または微生物由来の蛋
白質加水分解物またはその誘導体を2剤型染毛剤に含有
させる場合は、第1剤、第2剤のいずれでもよいが、通
常、第1剤に含有させるのが適している。
When the above-mentioned animal or plant and / or microorganism-derived protein hydrolyzate or its derivative is contained in a two-part hair dye, either the first part or the second part may be used. It is suitable to contain.

【0029】2剤型の酸化型染毛剤の場合、通常、第1
剤には酸化染料(染料中間体)および必要に応じてカッ
プラーを含有させ、第2剤には酸化剤を含有させる。
In the case of a two-part oxidized hair dye, the first dye is usually used.
The agent contains an oxidation dye (dye intermediate) and, if necessary, a coupler, and the second agent contains an oxidizing agent.

【0030】第1剤の酸化染料(染料中間体)として
は、公知のものを使用することができ、たとえば、p−
フェニレンジアミン、N−フェニル−p−フェニレンジ
アミンなどのフェニレンジアミン類、トルエン−2,5
−ジアミン、トルエン−3,4−ジアミンなどのトルエ
ンアミン類、p−アミノフェノール、p−メチルアミノ
フェノールなどのアミノフェノール類、o−アミノ−m
−ニトロフェノールなどのアミノニトロフェノール類、
2,6−ジアミノピリジンなどのジアミノピリジンなど
が使用できる。
As the oxidation dye (dye intermediate) of the first agent, known dyes can be used.
Phenylenediamines such as phenylenediamine, N-phenyl-p-phenylenediamine, toluene-2,5
-Diamines, tolueneamines such as toluene-3,4-diamine, aminophenols such as p-aminophenol and p-methylaminophenol, o-amino-m
-Aminonitrophenols such as nitrophenol,
A diaminopyridine such as 2,6-diaminopyridine can be used.

【0031】また、カップラーとしては、たとえば、m
−フェニレンジアミン、トルエン−2,4−ジアミン、
m−アミノフェノール、レゾルシン、カテコールなどが
使用できる。
As the coupler, for example, m
Phenylenediamine, toluene-2,4-diamine,
m-Aminophenol, resorcin, catechol and the like can be used.

【0032】第2剤の酸化剤としては、たとえば、過酸
化水素、過ホウ素酸ナトリウム、過酸化ナトリウムなど
が使用できる。
As the oxidizing agent of the second agent, for example, hydrogen peroxide, sodium perborate, sodium peroxide and the like can be used.

【0033】さらに、従来の染毛剤と同様に、各種のも
のを含有させることができる。たとえば、第1剤には非
イオン性界面活性剤、アニオン性界面活性剤、カチオン
性界面活性剤、両性界面活性剤などの界面活性剤、グリ
セリン、プロピレングリコールなどの溶解剤、保湿剤、
カルボキシメチルセルロース、ヒドロキシエチルセルロ
ースなどの粘度調整剤、その他、pH調整剤、香料など
の物質を適宜含有させることができる。
Further, various types of hair dyes can be contained in the same manner as the conventional hair dyes. For example, the first agent includes a nonionic surfactant, an anionic surfactant, a cationic surfactant, a surfactant such as an amphoteric surfactant, a dissolving agent such as glycerin and propylene glycol, a humectant,
Viscosity modifiers such as carboxymethylcellulose and hydroxyethylcellulose, and other substances such as pH adjusters and fragrances can be appropriately contained.

【0034】[0034]

【発明の効果】本発明の染毛剤は、染毛の立ち上がりが
速く、均一に染毛でき、しかも染毛後の毛髪の耐シャン
プー性が優れ、かつ染毛時の毛髪の損傷が少なく、染毛
後の毛髪に艶や潤いなどを付与することができる。
EFFECTS OF THE INVENTION The hair dye of the present invention has a rapid rise of hair dye, can uniformly dye hair, has excellent shampoo resistance of hair after dyeing, and has little damage to hair at the time of hair dyeing. Gloss and moisture can be imparted to the hair after dyeing.

【0035】[0035]

【実施例】つぎに、実施例を挙げて本発明をより具体的
に説明する。ただし、本発明はそれらの実施例のみに限
定されるものではない。
Next, the present invention will be described more specifically with reference to examples. However, the present invention is not limited to only these examples.

【0036】実施例1〜6および比較例1 表1および表2に示す組成の染毛剤(酸化型染毛剤)の
第1剤を調製した。なお、表中の各成分の配合量は重量
部であり、配合量が固形分量でないものについては、成
分名の後に括弧書きで固形分濃度を示している。また、
濃度を示す%は重量%である。これらは、以後の実施
例、比較例でも同様であり、調製にあたって使用した蛋
白質加水分解物(加水分解タンパク)の数平均分子量な
どについては表2の後にまとめて示す。
Examples 1 to 6 and Comparative Example 1 A first hair dye (oxidized hair dye) having the composition shown in Tables 1 and 2 was prepared. In addition, the compounding quantity of each component in a table | surface is a weight part, and when a compounding quantity is not a solid content, the solid content concentration is shown in parentheses after the component name. Also,
% Indicating the concentration is% by weight. These are the same in the following Examples and Comparative Examples. The number average molecular weight of the protein hydrolyzate (hydrolyzed protein) used in the preparation is collectively shown after Table 2.

【0037】[0037]

【表1】 [Table 1]

【0038】[0038]

【表2】 [Table 2]

【0039】※1:成和化成社製プロモイスWK(数平
均分子量400) ※2:成和化成社製プロモイスW−42R(数平均分子
量1000) ※3:成和化成社製プロモイスシルク−1000P(数
平均分子量1000) ※4:成和化成社製プロモイスWG(数平均分子量60
0) ※5:成和化成社製プロモイスWS(数平均分子量40
0) ※6:成和化成社製プロモイスWY(数平均分子量40
0)
* 1: Promois WK manufactured by Seiwa Kasei Co., Ltd. (number average molecular weight: 400) * 2: Promois W-42R manufactured by Seiwa Kasei Co., Ltd. (number average molecular weight: 1,000) * 3: Promois Silk-1000P manufactured by Seiwa Kasei (Number average molecular weight 1000) * 4: Promois WG manufactured by Seiwa Kasei Co., Ltd. (number average molecular weight 60
0) * 5: Promois WS manufactured by Seiwa Kasei Co., Ltd. (number average molecular weight 40
0) * 6: Promois WY manufactured by Seiwa Kasei Co., Ltd. (number average molecular weight 40
0)

【0040】上記第1剤に対し、第2剤は実施例1〜
6、比較例1とも共通で、下記の組成からなるものであ
る。ただし、各成分の配合量は重量部である。
In contrast to the above-mentioned first agent, the second agent was obtained in Examples 1 to
6, which is common to Comparative Example 1 and has the following composition. However, the amount of each component is part by weight.

【0041】第2剤 ステアリン酸 1.0 モノステアリン酸グリセリン 1.5 ポリオキシエチレンオレイルエーテル 1.0 過酸化水素水(35%) 15.0 精製水 計100とする Second agent Stearic acid 1.0 Glycerin monostearate 1.5 Polyoxyethylene oleyl ether 1.0 Hydrogen peroxide (35%) 15.0 Purified water Total 100

【0042】上記実施例1〜6および比較例1の染毛剤
を用いて、それぞれ重さ1gで長さ10cmの毛束を染
毛した。なお、染毛に先立ち、毛束は2%ポリオキシエ
チレンノニルフェニルエーテル水溶液で洗浄した後、水
洗し、脱色および毛髪の損傷度合いを均一にするため
に、5%の過酸化水素水を含む5%アンモニア水に5分
間浸漬してブリーチ処理を行い、水洗後、乾燥して染毛
処理のための前処理を行った。
Using the hair dyes of Examples 1 to 6 and Comparative Example 1, hair bundles each weighing 1 g and having a length of 10 cm were dyed. Prior to hair dyeing, the hair bundle was washed with a 2% aqueous solution of polyoxyethylene nonyl phenyl ether, and then washed with water. In order to decolorize and evenly damage the hair, 5% aqueous hydrogen peroxide was used. The resultant was immersed in 5% aqueous ammonia for 5 minutes to perform a bleaching treatment, washed with water, dried, and subjected to a pretreatment for a hair dyeing treatment.

【0043】染毛処理は、それぞれの第1剤と第2剤を
同量ずつ混合し、その混合物2gずつをそれぞれの毛束
に塗布した後、15分間放置し、お湯ですすぎ、ついで
2%ポリオキシエチレンノニルフェニルエーテル水溶液
で洗浄することによって行った。染毛処理後、ドライヤ
ーで毛束を乾燥し、実施例1〜6および比較例1につい
て5人のパネラーに、最も濃く染まっているものを1位
とし、最も染まりの悪いものを7位として順位をつけさ
せた。
In the hair dyeing treatment, the first agent and the second agent are mixed in equal amounts, and 2 g of the mixture is applied to each hair bundle, left for 15 minutes, rinsed with hot water, and then 2% This was performed by washing with an aqueous solution of polyoxyethylene nonylphenyl ether. After the hair dyeing treatment, the hair bundle was dried with a dryer, and ranks were ranked highest among the five panelists in Examples 1 to 6 and Comparative Example 1 with the darkest dye being ranked first and the worst dyed seventh. I was attached.

【0044】また、染毛後の毛髪の均染性、潤い、艶お
よび櫛通り性について下記の評価基準で比較例1と比較
評価させた。
The leveling property, moisture, gloss and combability of the hair after dyeing were evaluated in comparison with Comparative Example 1 according to the following evaluation criteria.

【0045】評価基準 +3:比較例1に比べて非常に良い +2:比較例1に比べて良い +1:比較例1に比べてやや良い 0:比較例1とほぼ同じ −1:比較例1に比べてやや悪い −2:比較例1に比べて悪い −3:比較例1に比べて非常に悪い Evaluation criteria +3: very good compared to comparative example 1 +2: good compared to comparative example 1 +1: slightly better than comparative example 1 0: almost the same as comparative example 1 -1: comparative example 1 Slightly worse than -2: worse than Comparative Example 1 -3: very worse than Comparative Example 1

【0046】さらに、上記実施例1〜6および比較例1
の染毛剤で染毛後の毛髪を2%ポリオキシエチレンノニ
ルフェニルエーテル水溶液で洗浄、水洗、ドライヤー乾
燥を5回繰り返し、洗浄後の毛髪の色の濃さ、潤い、艶
および櫛通り性について、前記染毛後の均染性などと同
様の評価基準で比較例1と比較評価することによって、
耐シャンプー性を評価した。それらの結果を表3に示す
が、評価値は5人のパネラーの平均値で示す。
Further, the above Examples 1 to 6 and Comparative Example 1
Wash the hair after dyeing with a 2% aqueous solution of polyoxyethylene nonyl phenyl ether, wash with water and dry with a dryer 5 times, and check the color depth, moisture, gloss and combability of the washed hair By performing comparative evaluation with Comparative Example 1 on the same evaluation criteria as the leveling properties after the hair dyeing,
The shampoo resistance was evaluated. The results are shown in Table 3, and the evaluation values are shown as the average values of five panelists.

【0047】[0047]

【表3】 [Table 3]

【0048】表3に示す結果から明らかなように、染毛
による色の濃さに関しては、実施例1〜6はいずれも比
較例1より、順位が高く(つまり、順位を示す数値が小
さく)、実施例1〜6は比較例1に比べて、毛髪を濃く
染めることが明らかにされていた。また、実施例の中で
は、加水分解ケラチンを含有させた実施例1(表1参
照)が最も良く、次いで加水分解コラーゲンを含有させ
た実施例2(表1参照)が良かった。
As is evident from the results shown in Table 3, with respect to the color strength due to hair dyeing, Examples 1 to 6 all have higher ranks (ie, smaller numerical values indicating the ranks) than Comparative Example 1. In Examples 1 to 6, it was revealed that the hair was dyed deeper than Comparative Example 1. Among the examples, Example 1 (see Table 1) containing hydrolyzed keratin was the best, and Example 2 (see Table 1) containing hydrolyzed collagen was next best.

【0049】比較例1のような従来の染毛剤では、一般
に染毛剤を毛髪に塗布した後30分間放置して発色を完
結させるため、上記試験のように染毛剤塗布後15分間
の放置では充分に発色していないと考えられるが、実施
例1〜6の染毛剤はいずれも15分間の放置で比較例1
より毛髪を濃く染めていて、加水分解ケラチンなどの蛋
白質加水分解物を染毛剤中に含有させると、染毛剤の染
色時間を短縮できることが明らかにされていた。
In the case of the conventional hair dye such as Comparative Example 1, since the hair dye is generally applied to the hair and left for 30 minutes to complete the color development, the hair dye is applied for 15 minutes after the hair dye is applied as in the above test. It is considered that the color was not sufficiently developed on standing, but the hair dyes of Examples 1 to 6 were all left for 15 minutes to obtain Comparative Example 1
It has been revealed that hair is dyed more densely, and that if a protein hydrolyzate such as hydrolyzed keratin is contained in the hair dye, the dyeing time of the hair dye can be shortened.

【0050】また、染毛後の毛髪の均染性、潤い、艶、
櫛通り性については、加水分解ケラチンなどの蛋白質加
水分解物を含有させた実施例1〜6はいずれも比較例1
に比べてプラス(+)の評価であって、染毛剤中に含有
させた加水分解ケラチンなどの蛋白質加水分解物が毛髪
を均一に染毛し、染毛時の毛髪を保護して染毛による毛
髪の損傷を防止する効果を有する(これは櫛通り性が良
好なことから判断できる)ことが明らかにされていた。
Also, the leveling, moisturizing, gloss,
Regarding combability, Comparative Examples 1 to 6 each containing a protein hydrolyzate such as hydrolyzed keratin were used.
It is a positive (+) evaluation compared to that of the above. The protein hydrolyzate such as hydrolyzed keratin contained in the hair dye uniformly dyes the hair, and protects the hair at the time of hair dyeing and dyes the hair. It has been found that the compound has an effect of preventing the hair from being damaged (this can be judged from the good combability).

【0051】さらに、シャンプーで5回洗浄後も、実施
例1〜6で染毛した毛髪は、いずれも比較例1で染毛し
た毛髪に比べて色が濃く、また、毛髪の潤い、艶、櫛通
り性のいずれの項目においても実施例1〜6は比較例1
より優れていて、加水分解ケラチンなどの蛋白質加水分
解物を染毛剤中に含有させると、染毛後の毛髪の耐シャ
ンプー性が向上することが明らかにされていた。
Furthermore, even after washing five times with shampoo, the hair dyed in Examples 1 to 6 is all darker in color than the hair dyed in Comparative Example 1, and has moisture, gloss, In each of the items of combability, Examples 1 to 6 are Comparative Examples 1
It has been revealed that when a protein hydrolyzate such as hydrolyzed keratin is contained in a hair dye, the shampoo resistance of the hair after hair dyeing is improved.

【0052】実施例7〜10および比較例2 表4および表5に示す組成の染毛剤第1剤を調製した。
使用した蛋白質加水分解物やその誘導体の蛋白質加水分
解物部分の数平均分子量は表5の後で説明する。
Examples 7 to 10 and Comparative Example 2 The first hair dye compositions having the compositions shown in Tables 4 and 5 were prepared.
The number average molecular weight of the used protein hydrolyzate and the protein hydrolyzate portion of the derivative thereof will be described after Table 5.

【0053】[0053]

【表4】 [Table 4]

【0054】[0054]

【表5】 [Table 5]

【0055】使用した加水分解ケラチンの数平均分子量
は1000であり、塩化N−〔2−ヒドロキシ−3−
(トリメチルアンモニオ)プロピル〕加水分解ケラチン
における加水分解ケラチンの数平均分子量は1000
で、塩化N−〔2−ヒドロキシ−3−(ヤシ油アルキル
ジメチルアンモニオ)プロピル〕加水分解ケラチンにお
ける加水分解ケラチンの数平均分子量は1000であ
り、ヤシ油脂肪酸加水分解ケラチンカリウムは数平均分
子量1000の加水分解ケラチンとヤシ油脂肪酸との縮
合物のカリウム塩である。
The number average molecular weight of the hydrolyzed keratin used was 1000 and N- [2-hydroxy-3-chloride was used.
(Trimethylammonio) propyl] hydrolyzed keratin has a number average molecular weight of 1000
The number average molecular weight of hydrolyzed keratin in N- [2-hydroxy-3- (coconut oil alkyldimethylammonio) propyl] hydrolyzed keratin is 1000, and the number average molecular weight of coconut oil fatty acid hydrolyzed keratin potassium is 1000. Is a potassium salt of a condensate of keratin and coconut oil fatty acid.

【0056】上記第1剤に対して第2剤は、実施例7〜
10、比較例2とも共通で、下記の組成からなるもので
ある。ただし、各成分の配合量は重量部である。
With respect to the first agent, the second agent was used in Examples 7 to
10 and Comparative Example 2 are common and have the following composition. However, the amount of each component is part by weight.

【0057】第2剤 35%過酸化水素水 15.0 リン酸 0.1 精製水 計100とする Second agent 35% aqueous hydrogen peroxide 15.0 Phosphoric acid 0.1 Purified water Total 100

【0058】上記実施例7〜10および比較例2の染毛
剤を用いて、それぞれ重さ1gで長さ10cmの毛束を
染毛した。染毛にあたっては、実施例1と同様に前処理
をして、各毛束の脱色および毛髪の損傷の度合いを均一
にした。そして、染毛処理は、それぞれの第1剤と第2
剤を同量ずつ混合し、その混合物2gずつをそれぞれの
毛束に塗布した後、20分間放置し、お湯ですすぎ、つ
いで2%ポリオキシエチレンノニルフェニルエーテル水
溶液で洗浄することによって行った。染毛処理後、ドラ
イヤーで毛束を乾燥し、実施例7〜10および比較例2
について5人のパネラーに、最も濃く染まっているもの
を1位とし、最も染まりの悪いものを5位として順位を
つけさせた。
Using the hair dyes of Examples 7 to 10 and Comparative Example 2, hair bundles each weighing 1 g and having a length of 10 cm were dyed. For hair dyeing, pretreatment was performed in the same manner as in Example 1 to uniform the degree of bleaching of each hair bundle and damage to the hair. Then, the hair dyeing treatment is performed for each of the first agent and the second agent.
The same amount of the agent was mixed, and 2 g of the mixture was applied to each hair bundle, allowed to stand for 20 minutes, rinsed with hot water, and then washed with a 2% aqueous solution of polyoxyethylene nonylphenyl ether. After the hair dyeing treatment, the hair bundle was dried with a dryer, and Examples 7 to 10 and Comparative Example 2
5 panelists were ranked first with the darkest dye and fifth with the least stained.

【0059】また、染毛後の均染性、毛髪の潤い、艶お
よび櫛通り性について実施例1と同様の評価基準で比較
例2と比較評価させた。
The leveling properties, hair moistness, gloss, and combability after hair dyeing were compared with Comparative Example 2 using the same evaluation criteria as in Example 1.

【0060】さらに、上記実施例7〜10および比較例
2の染毛剤で染毛後の毛髪を実施例1と同様にシャンプ
ー処理を5回繰り返し、洗浄後の毛髪の色の濃さ、潤
い、艶および櫛通り性について、実施例1と同様の評価
基準で比較例2と比較評価することによって、耐シャン
プー性を評価した。それらの結果を表6に示すが、評価
値は5人のパネラーの平均値である。
Further, the hair after dyeing with the hair dyes of Examples 7 to 10 and Comparative Example 2 was subjected to shampooing treatment 5 times in the same manner as in Example 1, and the color depth and moisture of the washed hair were repeated. The shampoo resistance was evaluated by comparing the gloss, gloss and combability with Comparative Example 2 using the same evaluation criteria as in Example 1. The results are shown in Table 6, and the evaluation values are the average values of five panelists.

【0061】[0061]

【表6】 [Table 6]

【0062】表6に示す結果から明らかなように、染毛
による色の濃さに関しては実施例7〜10はいずれも比
較例2に比べて毛髪を濃く染めていて、染毛剤中に含有
させた加水分解ケラチンなどの蛋白質加水分解物やその
誘導体が毛髪を濃く染めるのに有効に作用することが明
らかにされていた。また、実施例の中では、塩化N−
〔2−ヒドロキシ−3−(トリメチルアンモニオ)プロ
ピル〕加水分解ケラチンを含有させた実施例8(表4参
照)が最も良く、次いで塩化N−〔2−ヒドロキシ−3
−(ヤシ油アルキルジメチルアンモニオ)プロピル〕加
水分解ケラチンを含有させた実施例9(表4参照)、ア
シル化物のヤシ油脂肪酸加水分解ケラチンカリウムを含
有させた実施例10(表5参照)、加水分解ケラチンを
含有させた実施例7(表4参照)の順であった。
As is clear from the results shown in Table 6, with respect to the color strength due to hair dyeing, all of Examples 7 to 10 dye the hair deeper than Comparative Example 2, and contained in the hair dye. It has been clarified that protein hydrolyzates such as hydrolyzed keratin and derivatives thereof are effective in deeply dyeing hair. In Examples, N-chloride N-
Example 8 (see Table 4) containing [2-hydroxy-3- (trimethylammonio) propyl] hydrolyzed keratin is best followed by N- [2-hydroxy-3 chloride.
-(Coco oil alkyl dimethyl ammonium) propyl] Example 9 containing hydrolyzed keratin (see Table 4), Example 10 containing acylated coconut fatty acid hydrolyzed keratin potassium as coconut oil (see Table 5), Example 7 (see Table 4) in which hydrolyzed keratin was contained was in order.

【0063】また、染毛後の毛髪の均染性、潤い、艶、
櫛通り性については、蛋白質加水分解物やその誘導体を
含有させた実施例7〜10はいずれも比較例2に比べて
プラス(+)の評価であって、蛋白質加水分解物やその
誘導体が毛髪を均一に染毛し、染毛時の毛髪を保護して
染毛による毛髪の損傷を防止する効果を有することが明
らかにされていた。さらに、シャンプーで5回洗浄後
も、実施例7〜10で染毛した毛髪は、いずれも比較例
2で染毛した毛髪に比べて、いずれの項目においても評
価値が高く、耐シャンプー性が向上していることが明ら
かにされていた。
In addition, the leveling property, moisture, gloss,
With respect to combability, Examples 7 to 10 in which the protein hydrolyzate and its derivative were contained were evaluated as positive (+) as compared with Comparative Example 2, and the protein hydrolyzate and its derivative were Has been shown to have an effect of uniformly dyeing the hair, protecting the hair at the time of hair dyeing, and preventing damage to the hair due to hair dyeing. Furthermore, even after washing five times with shampoo, the hair dyed in Examples 7 to 10 had higher evaluation values in all items than the hair dyed in Comparative Example 2, and the shampoo resistance was higher. It was clear that it had improved.

【0064】実施例11〜12および比較例3 表7に示す組成の染毛剤を調製し、染毛処理時間による
染毛度の違いを評価した。上記染毛剤の第1剤の調製に
あたって使用した塩化N−〔2−ヒドロキシ−3−(ト
リメチルアンモニオ)プロピル〕加水分解ケラチンにお
ける加水分解ケラチンの数平均分子量は400で、ヤシ
油脂肪酸加水分解コラーゲンカリウムにおける加水分解
コラーゲンの数平均分子量は400であった。
Examples 11 to 12 and Comparative Example 3 Hair dyes having the compositions shown in Table 7 were prepared, and the difference in the degree of hair dyeing depending on the hair dyeing treatment time was evaluated. The number average molecular weight of hydrolyzed keratin in N- [2-hydroxy-3- (trimethylammonio) propyl] hydrolyzed keratin used in the preparation of the first hair dye was 400, and coconut oil fatty acid hydrolysis The number average molecular weight of the hydrolyzed collagen in collagen potassium was 400.

【0065】[0065]

【表7】 [Table 7]

【0066】上記実施例11〜12および比較例3の第
1剤と第2剤をそれぞれの同量ずつ混合し、その混合物
2gずつを用いて、それぞれ重さ1gで長さ10cmの
毛束を染毛した。染毛にあたっては、実施例1と同様に
前処理して各毛束の脱色および毛髪の損傷の度合いを均
一にした。そして、染毛処理では、実施例11および実
施例12用に毛束を各5束用意し、それぞれの毛束に実
施例11および実施例12の染毛剤をそれぞれ2gずつ
塗布し、塗布後の放置時間を10分、15分、20分、
25分および30分とし、各放置時間の終了後直ちに毛
束をぬるま湯ですすぎ、2%ポリオキシエチレンノニル
フェニルエーテル水溶液で洗浄し、ぬるま湯ですすいだ
後、ヘアードライヤーで乾燥した。そして、比較例3の
場合は、毛束に染毛剤を塗布後30分間放置し、上記実
施例11などと同様に毛束をぬるま湯ですすぎ、2%ポ
リオキシエチレンノニルフェニルエーテル水溶液で洗浄
し、ぬるま湯ですすいだ後、ヘアードライヤーで乾燥し
た。
The first agent and the second agent of the above Examples 11 to 12 and Comparative Example 3 were mixed in equal amounts, and 2 g of each mixture was used to prepare a hair bundle of 1 g in weight and 10 cm in length. I dyed hair. In the case of hair dyeing, pretreatment was performed in the same manner as in Example 1 so that the degree of bleaching of each hair bundle and the degree of damage to the hair were uniform. In the hair dyeing treatment, five hair bundles were prepared for each of Examples 11 and 12, and 2 g of each of the hair dyes of Example 11 and Example 12 was applied to each hair bundle. 10 minutes, 15 minutes, 20 minutes,
Immediately after each standing time, the hair bundle was rinsed with lukewarm water, washed with a 2% aqueous solution of polyoxyethylene nonylphenyl ether, rinsed with lukewarm water, and dried with a hair dryer. In the case of Comparative Example 3, the hair dye was applied to the hair bundle for 30 minutes, and the hair bundle was rinsed with lukewarm water and washed with a 2% aqueous solution of polyoxyethylene nonylphenyl ether in the same manner as in Example 11 above. After rinsing with lukewarm water, it was dried with a hair dryer.

【0067】乾燥後、実施例11〜12で染毛した毛束
の色の濃さと比較例3で染毛した毛束の色の濃さとを、
10人のパネラーに比較評価させた。実施例11の評価
結果を表8に示し、実施例12の評価結果を表9に示す
が、それらの評価結果は、比較例3より色が濃いと答え
た人数、比較例3より色が薄いと答えた人数、色の濃さ
はほぼ同じと答えた人数で示す。
After drying, the color density of the hair tresses dyed in Examples 11 to 12 and the color density of the hair tresses dyed in Comparative Example 3 were
Ten panelists were compared and evaluated. The evaluation results of Example 11 are shown in Table 8, and the evaluation results of Example 12 are shown in Table 9. The evaluation results show that the number of persons who answered that the color was darker than Comparative Example 3 and the color that was lighter than Comparative Example 3 The number of people who answered that the color depth was almost the same.

【0068】[0068]

【表8】 [Table 8]

【0069】[0069]

【表9】 [Table 9]

【0070】表8に示す結果から明らかなように、加水
分解ケラチンの第4級アンモニウム誘導体を含有させた
実施例11は、比較例3に比べて、処理時間が半分の1
5分でパネラーの多くが色の濃さはほぼ同じと答えてい
た。なお、処理時間が10分の段階で比較例3の方が色
が濃いと答えた人数が多い(すなわち、表8中の「比較
例3より色が薄いと答えた人数」が多い)のは、比較例
3は染毛剤の塗布後30分間放置していて、染毛剤の塗
布後の放置時間が長いことによるものである。
As is clear from the results shown in Table 8, Example 11 in which the quaternary ammonium derivative of hydrolyzed keratin was contained had a treatment time that was half that of Comparative Example 3 which was 1%.
In 5 minutes, many panelists answered that the color intensity was almost the same. The number of persons who answered that the color of the comparative example 3 was darker at the stage of the processing time of 10 minutes was large (that is, the number of persons who answered that the color was lighter than that of the comparative example 3 in Table 8 was large). In Comparative Example 3, the coating was left for 30 minutes after the application of the hair dye, and this was due to the long standing time after the application of the hair dye.

【0071】また、表9に示すように、加水分解コラー
ゲンのアシル化物の塩を含有させた実施例12は、処理
時間が20分でパネラーのほぼ全員が色の濃さは比較例
3とほぼ同じと答えていて、加水分解ケラチンの第4級
アンモニウム誘導体(実施例11の場合)や加水分解コ
ラーゲンのアシル化物の塩(実施例12の場合)が染毛
処理時間を短縮させることが明らかにされていた。
Further, as shown in Table 9, in Example 12 in which the salt of the acylated hydrolyzed collagen was contained, the treatment time was 20 minutes, and almost all of the panelists had almost the same color depth as Comparative Example 3. It is clear that the quaternary ammonium derivative of hydrolyzed keratin (in the case of Example 11) and the salt of the acylated product of the hydrolyzed collagen (in the case of Example 12) shorten the hair dyeing treatment time. It had been.

─────────────────────────────────────────────────────
────────────────────────────────────────────────── ───

【手続補正書】[Procedure amendment]

【提出日】平成9年3月4日[Submission date] March 4, 1997

【手続補正1】[Procedure amendment 1]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0039[Correction target item name] 0039

【補正方法】変更[Correction method] Change

【補正内容】[Correction contents]

【0039】※1:成和化成社製プロモイスWK(数平
均分子量400) ※2:成和化成社製プロモイスW−42R(数平均分子
量1000) ※3:成和化成社製プロモイスシルク−1000P(数
平均分子量1000) ※4:平均分子量60 ※5:平均分子量40 ※6:成和化成社製プロモイスWY(数平均分子量40
0)
* 1: Promois WK manufactured by Seiwa Kasei Co., Ltd. (number average molecular weight: 400) * 2: Promois W-42R manufactured by Seiwa Kasei Co., Ltd. (number average molecular weight: 1,000) * 3: Promois Silk-1000P manufactured by Seiwa Kasei (number average molecular weight 1000) ※ 4: The number-average molecular weight 60 0 ※ 5: The number-average molecular weight 40 0 ※ 6: Seiwa Kasei Co. Promois WY (number average molecular weight of 40
0)

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 酸化型の染毛剤において、動植物および
/または微生物由来の蛋白質加水分解物またはその誘導
体を1種以上含有させたことを特徴とする染毛剤。
1. An oxidized hair dye comprising one or more protein hydrolysates or derivatives thereof derived from animals and plants and / or microorganisms.
【請求項2】 動植物および/または微生物由来の蛋白
質加水分解物が、加水分解ケラチンまたは加水分解コラ
ーゲンである請求項1記載の染毛剤。
2. The hair dye according to claim 1, wherein the protein hydrolyzate derived from animals, plants and / or microorganisms is hydrolyzed keratin or hydrolyzed collagen.
【請求項3】 動植物および/または微生物由来の蛋白
質加水分解物の誘導体が、蛋白質加水分解物の第4級ア
ンモニウム誘導体である請求項1または2記載の染毛
剤。
3. The hair dye according to claim 1, wherein the derivative of the protein hydrolyzate derived from animals and plants and / or microorganisms is a quaternary ammonium derivative of the protein hydrolyzate.
【請求項4】 動植物および/または微生物由来の蛋白
質加水分解物の誘導体が、蛋白質加水分解物のアシル化
物またはその塩である請求項1または2記載の染毛剤。
4. The hair dye according to claim 1, wherein the derivative of the protein hydrolyzate derived from animals and plants and / or microorganisms is an acylated protein hydrolyzate or a salt thereof.
JP35489396A 1996-12-20 1996-12-20 Hair dyeing agent Pending JPH10182371A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP35489396A JPH10182371A (en) 1996-12-20 1996-12-20 Hair dyeing agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP35489396A JPH10182371A (en) 1996-12-20 1996-12-20 Hair dyeing agent

Publications (1)

Publication Number Publication Date
JPH10182371A true JPH10182371A (en) 1998-07-07

Family

ID=18440626

Family Applications (1)

Application Number Title Priority Date Filing Date
JP35489396A Pending JPH10182371A (en) 1996-12-20 1996-12-20 Hair dyeing agent

Country Status (1)

Country Link
JP (1) JPH10182371A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000226319A (en) * 1999-02-04 2000-08-15 Pola Chem Ind Inc Hair dye
JP2002097121A (en) * 2000-09-20 2002-04-02 Hoyu Co Ltd Oxidative hair dyeing composition
JP2002308746A (en) * 2001-04-05 2002-10-23 Dongsung Pharm Co Ltd Composition for hairdye
JP2002322035A (en) * 2001-02-20 2002-11-08 Nakano Seiyaku Kk Pretreatment agent for hair color, treatment agent for hair color and method for treating hair
JP2002338443A (en) * 2001-05-23 2002-11-27 Kanebo Ltd Hair dye or bleaching agent composition

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000226319A (en) * 1999-02-04 2000-08-15 Pola Chem Ind Inc Hair dye
JP2002097121A (en) * 2000-09-20 2002-04-02 Hoyu Co Ltd Oxidative hair dyeing composition
JP2002322035A (en) * 2001-02-20 2002-11-08 Nakano Seiyaku Kk Pretreatment agent for hair color, treatment agent for hair color and method for treating hair
JP2002308746A (en) * 2001-04-05 2002-10-23 Dongsung Pharm Co Ltd Composition for hairdye
JP2002338443A (en) * 2001-05-23 2002-11-27 Kanebo Ltd Hair dye or bleaching agent composition

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