JPH0717836A - Hair dye composition - Google Patents

Hair dye composition

Info

Publication number
JPH0717836A
JPH0717836A JP18936693A JP18936693A JPH0717836A JP H0717836 A JPH0717836 A JP H0717836A JP 18936693 A JP18936693 A JP 18936693A JP 18936693 A JP18936693 A JP 18936693A JP H0717836 A JPH0717836 A JP H0717836A
Authority
JP
Japan
Prior art keywords
hair
hair dye
cationized
dye composition
salt
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP18936693A
Other languages
Japanese (ja)
Other versions
JP2872888B2 (en
Inventor
Shigeharu Iyoda
重治 伊豫田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hoyu Co Ltd
Original Assignee
Hoyu Co Ltd
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Priority to JP18936693A priority Critical patent/JP2872888B2/en
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Abstract

PURPOSE:To obtain a hair dye composition having high stability, composed of easily miscible 1st liquid and 2nd liquid and providing excellent dyed hair having excellent feeling. CONSTITUTION:This hair dye composition contains (A) 0.01-10wt.% (preferably 0.1-5wt.%) of an acylated collagen polypeptide of the formula (R1 is fatty acid, preferably coconut oil fatty acid or lauric acid; M is inorganic salt or organic salt; R2 is various groups found in amino acids) and (B) 0.01-5wt.% (preferably 0.1-3wt.%) of a water-soluble cationized polymer containing amino group or ammonium group bonded to the polymer chain or at least dimethyldiallylammonium halide as a constituent unit, e.g. cationized starch, cationized guar gum derivative and quaternarized polyvinyl pyrrolidone derivative, preferably cationized cellulose derivative or diallyl-quaternary ammonium salt/acrylamide copolymer.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は、安定性が良好で、1剤
と2剤の混合が容易であり、しかも染め上がりが良好で
かつ染毛後の毛髪の感触にも優れる染毛剤組成物に関す
る。
FIELD OF THE INVENTION The present invention relates to a hair dye composition having good stability, easy mixing of one agent and two agents, good dyeing and excellent feel of hair after dyeing. Regarding

【0002】[0002]

【従来の技術】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2
剤型の酸化染毛剤が広く利用されている。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、毛髪の中で酸化重合を行うことにより色素を生成さ
せ、毛髪を染着するものである。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おり、非常に便利なものであっ
た。
2. Description of the Related Art Conventionally, a hair dye is composed of a first agent containing an oxidizing dye intermediate and a second agent containing an oxidizing agent.
A dosage form of oxidative hair dye is widely used. The oxidative hair dye is one in which a colorless, low-molecular weight oxidative dye intermediate is permeated into the hair and oxidatively polymerized in the hair to generate a pigment, which dyes the hair. These hair dyes are very convenient because they can dye hair in various color tones as desired and have excellent hair dyeing power.

【0003】[0003]

【発明が解決しようとする課題】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。この傾向は、製剤中に溶剤や界面活性剤、アンモ
ニア等のアルカリ剤が多量に配合されている液体式染毛
剤において顕著であった。一方、クリーム式の染毛剤で
は液体式で見られた欠点を多少改善できるが、その効果
は充分満足できる程のものではなかった。更にクリーム
式の染毛剤はその1剤中に多量の染料を配合するために
乳化物の安定性が悪くなるという問題があった。このた
め、これまでは高級アルコールや炭化水素等の増粘成分
を大量に加えて、製剤の安定性を確保してきた。しかし
このようなものは、実際に使用する際、1剤と2剤の粘
度の違いから混合が困難になったり、経時変化によって
粘度が上がりチューブから絞り出すことが困難になる等
の欠点を併せ持っていた。本発明は、上記のような欠点
を持たない染毛剤組成物を提供することを目的とする。
However, in the conventional oxidative hair dye, the hair is apt to be damaged by the hair dyeing treatment. This tendency was remarkable in a liquid hair dye in which a large amount of a solvent, a surfactant, and an alkaline agent such as ammonia were mixed in the preparation. On the other hand, the cream type hair dye can improve the drawbacks found in the liquid type to some extent, but the effect was not sufficiently satisfactory. Further, the cream type hair dye has a problem that the stability of the emulsion is deteriorated because a large amount of dye is mixed in the one agent. Therefore, until now, a large amount of thickening components such as higher alcohols and hydrocarbons have been added to ensure the stability of the preparation. However, such a product also has drawbacks such as difficulty in mixing due to the difference in viscosity between the first agent and the second agent, and difficulty in squeezing out from the tube due to increase in viscosity over time when actually used. It was It is an object of the present invention to provide a hair dye composition that does not have the above-mentioned drawbacks.

【0004】[0004]

【課題を解決するための手段】本発明者は、上記欠点を
解決するために、鋭意検討した結果、アシル化コラーゲ
ンポリペプタイドとカチオン化ポリマーからなる染毛剤
組成物が、安定性が良好で、1剤と2剤の混合が容易で
あり、しかも染め上がりが良好でかつ染毛後の毛髪の感
触にも優れることを見いだし、本発明を完成するに至っ
た。
Means for Solving the Problems As a result of intensive studies for solving the above-mentioned drawbacks, the present inventor has found that a hair dye composition comprising an acylated collagen polypeptide and a cationized polymer has good stability. It was found that the 1st and 2nd agents can be easily mixed, the dyeing is good, and the feeling of the hair after dyeing is excellent, and the present invention has been completed.

【0005】本発明に使用されるアシル化コラーゲンポ
リペプタイドは、下記の一般式で表わされる。
The acylated collagen polypeptide used in the present invention is represented by the following general formula.

【0006】[0006]

【化1】 式(1)中、R1は脂肪酸、Mは無機塩または有機塩、
R2はアミノ酸中に見い出される種々の基を表わす。こ
の脂肪酸としては、例えばヤシ油脂肪酸、ラウリン酸、
ウンデシレン酸、イソステアリン酸等があげられ、この
中でも特にヤシ油脂肪酸又はラウリン酸が好ましい。無
機塩または有機塩としては、例えばナトリウム塩、カリ
ウム塩、トリエタノールアミン塩、アミノメチルプロパ
ンジオール塩等があげられ、この中でも特に、カリウム
塩またはナトリウム塩が好ましい。市販品としては、
(株)成和化成のプロモイスECP,ECT,ECS,
EUP,EUT,EMP,EMT,ELP,ELT,E
118D,ESP,ESS,EOP,EOSなどが挙げ
られる。その配合量としては、0.01〜10重量%が
好ましく、更に好ましくは0.1〜5重量%である。
[Chemical 1] In the formula (1), R1 is a fatty acid, M is an inorganic salt or an organic salt,
R2 represents the various groups found in amino acids. Examples of this fatty acid include coconut oil fatty acid, lauric acid,
Examples thereof include undecylenic acid and isostearic acid. Among them, coconut oil fatty acid or lauric acid is particularly preferable. Examples of the inorganic salt or organic salt include sodium salt, potassium salt, triethanolamine salt, aminomethylpropanediol salt and the like, and among these, potassium salt or sodium salt is particularly preferable. As a commercial product,
Promote ECP, ECT, ECS of Seiwa Kasei Co., Ltd.
EUP, EUT, EMP, EMT, ELP, ELT, E
118D, ESP, ESS, EOP, EOS, etc. are mentioned. The blending amount is preferably 0.01 to 10% by weight, more preferably 0.1 to 5% by weight.

【0007】また、本発明で用いられるカチオン化ポリ
マーは、ポリマー鎖に結合してアミノ基又はアンモニウ
ム基を含むか、又は少なくともジメチルジアリルアンモ
ニウムハライドを構成単位として含む水溶液のものであ
り、例えばカチオン化セルロース誘導体、カチオン性澱
粉 カチオン化グアーガム誘導体、ジアリル4級アンモ
ニウム塩/アクリルアミド共重合物及び4級化ポリビニ
ルピロリドン誘導体などが挙げられる。カチオン化セル
ロース誘導体としては例えば次の一般式(2)で表され
るものが好ましい。
The cationized polymer used in the present invention is an aqueous solution containing an amino group or an ammonium group bound to the polymer chain, or at least a dimethyldiallylammonium halide as a constituent unit. Cellulose derivative, cationic starch, cationized guar gum derivative, diallyl quaternary ammonium salt / acrylamide copolymer, quaternized polyvinylpyrrolidone derivative and the like can be mentioned. As the cationized cellulose derivative, for example, those represented by the following general formula (2) are preferable.

【0008】[0008]

【化2】 式(2)中、Aはアンヒドログルコース単位の残基を示
し、fは50〜20000の整数であり、各R3は、そ
れぞれ次の一般式(3)で表される置換基を示す。
[Chemical 2] In the formula (2), A represents a residue of anhydroglucose unit, f is an integer of 50 to 20000, and each R3 represents a substituent represented by the following general formula (3).

【0009】[0009]

【化3】 式(3)中、R4,R5は炭素数2又は3のアルキレン
基、gは0〜10の整数、hは0〜3の整数、iは0〜
10の整数、R6は炭素数1〜3のアルキレン基又はヒ
ドロキシアルキレン基、R7,R8,R9は同じか又は異
なっており炭素数10までのアルキル基、アリール基又
はアラルキル基を示し、また式中の窒素原子を含んで複
素環を形成してもよい。X1は陰イオン(塩素、臭素、
沃素、硫酸、スルホン酸、メチル硫酸、リン酸、硝酸
等)を示す。本発明に用いられるカチオン化セルロース
誘導体のカチオン置換度は、0.01〜1即ちアンヒド
ログルコース単位当りのhの平均値は、0.01〜1が
好ましく、更に好ましくは0.02〜0.5である。ま
た、g+iの合計は平均1〜3である。カチオン置換度
は、0.01未満では十分でなく、また1を超えてもか
まわないが反応収率の点より1以下が好ましい。ここで
用いるカチオン化セルロース誘導体の分子量は約100
000〜3000000の間が好ましい。市販品として
は、ライオン(株)のレオガードG,GP、ユニオンカ
ーバイド社のポリマーJR−125,JR−400,J
R−30M,LR−400,LR−30M等が挙げられ
る。
[Chemical 3] In formula (3), R4 and R5 are alkylene groups having 2 or 3 carbon atoms, g is an integer of 0 to 10, h is an integer of 0 to 3, and i is 0.
An integer of 10, R6 is an alkylene group having 1 to 3 carbon atoms or a hydroxyalkylene group, R7, R8 and R9 are the same or different and each represents an alkyl group having up to 10 carbon atoms, an aryl group or an aralkyl group; The heterocycle may be formed by containing the nitrogen atom of. X1 is an anion (chlorine, bromine,
Iodine, sulfuric acid, sulfonic acid, methyl sulfuric acid, phosphoric acid, nitric acid, etc.). The cation substitution degree of the cationized cellulose derivative used in the present invention is preferably 0.01 to 1, that is, the average value of h per anhydroglucose unit is preferably 0.01 to 1, and more preferably 0.02 to 0. It is 5. The total of g + i is 1 to 3 on average. The cation substitution degree is not sufficient if it is less than 0.01, and may be more than 1, but is preferably 1 or less from the viewpoint of reaction yield. The molecular weight of the cationized cellulose derivative used here is about 100.
It is preferably between 000 and 3,000,000. Commercially available products are Leoguard G and GP from Lion Corporation, and polymers JR-125, JR-400 and J from Union Carbide.
R-30M, LR-400, LR-30M, etc. are mentioned.

【0010】カチオン性澱粉としては次の一般式(4)
で表されるものが好ましい。
The cationic starch has the following general formula (4):
What is represented by is preferable.

【0011】[0011]

【化4】 式(4)中、Bは澱粉残基、R10はアルキレン基又はヒ
ドロキシアルキレン基、R11、R12、R13は同じか又は
異なっており、炭素数10以下のアルキル基、アリール
基又はアラルキル基を示し、また式中の窒素原子を含ん
で複素環を形成してもよい。 X2は陰イオン(塩素、臭
素、沃素、硫酸、スルホン酸、メチル硫酸、リン酸、硝
酸等)、jは正の整数を示す。本発明で用いられるカチ
オン性澱粉のカチオン置換度は0.01〜1、即ち無水
グルコース単位当たり0.01〜1、好ましくは0.0
2〜0.5個のカチオン基が導入されたものが好まし
い。カチオン置換度が0.01未満では十分でなく、ま
た1を超えてもかまわないが反応収率の点より1以下が
好ましい。
[Chemical 4] In the formula (4), B is a starch residue, R10 is an alkylene group or a hydroxyalkylene group, R11, R12 and R13 are the same or different, and each represents an alkyl group having 10 or less carbon atoms, an aryl group or an aralkyl group, In addition, the nitrogen atom in the formula may be included to form a heterocycle. X2 is an anion (chlorine, bromine, iodine, sulfuric acid, sulfonic acid, methyl sulfuric acid, phosphoric acid, nitric acid, etc.), and j is a positive integer. The degree of cation substitution of the cationic starch used in the present invention is 0.01 to 1, that is, 0.01 to 1 per anhydroglucose unit, preferably 0.0.
Those having 2 to 0.5 cationic groups introduced therein are preferable. If the degree of cation substitution is less than 0.01, it is not sufficient, and it may be more than 1, but it is preferably 1 or less from the viewpoint of reaction yield.

【0012】カチオン化グアーガム誘導体としては、次
の一般式(5)で表されるものが好ましい。
As the cationized guar gum derivative, those represented by the following general formula (5) are preferable.

【0013】[0013]

【化5】 式(5)中、Dはグアーガム残基、R14はアルキレン基
又はヒドロキシアルキレン基R15,R16,R17は同じか
又は異なっており、炭素数10以下のアルキル基、アリ
ール基又はアラルキル基を示し、また式中の窒素原子を
含んで複素環を形成してもよい。X3は陰イオン( 塩
素、臭素、沃素、硫酸、スルホン酸、メチル硫酸、リン
酸、硝酸等)、kは正の整数を示す。本発明で用いられ
るカチオン化グアーガム誘導体のカチオン置換度は0.
01〜1が好ましく、特に0.02〜0.5個のカチオ
ン基が、糖単位に導入されたものが好ましい。例えば、
特公昭58−35640号、特公昭60−46158号
及び、特開昭58−53996号公報に記載され、ジャ
グアール(セラニーズシュタイン・ホール社)として市
販されている。
[Chemical 5] In the formula (5), D is a guar gum residue, R14 is an alkylene group or a hydroxyalkylene group R15, R16 and R17 are the same or different and each represents an alkyl group having 10 or less carbon atoms, an aryl group or an aralkyl group, and The nitrogen atom in the formula may be included to form a heterocycle. X3 is an anion (chlorine, bromine, iodine, sulfuric acid, sulfonic acid, methyl sulfuric acid, phosphoric acid, nitric acid, etc.), and k is a positive integer. The cation substitution degree of the cationized guar gum derivative used in the present invention is 0.
01 to 1 is preferable, and one having 0.02 to 0.5 cationic groups introduced into the sugar unit is particularly preferable. For example,
It is described in JP-B-58-35640, JP-B-60-46158 and JP-A-58-53996, and is commercially available as Jaguar (Ceranistein Stein Hall).

【0014】カチオン性のジアリル4級アンモニウム塩
/アクリルアミド共重合物としては、次の一般式(6)又
は(7)で示されるものが好ましい。
As the cationic diallyl quaternary ammonium salt / acrylamide copolymer, those represented by the following general formula (6) or (7) are preferable.

【化6】 [Chemical 6]

【化7】 式(6)及び(7)中、R18,R19は同じか又は異なっ
ており、水素、アルキル基(炭素数1〜18)、フェニ
ル基、アリール基、ヒドロキシアルキル基、アミドアル
キル基、シアノアルキル基、アルコキシアルキル基、又
はカルボアルコキシアルキル基R20,R21,R22,R23
は同じか又は異なっており、水素、低級アルキル基(炭
素数1〜3)又はフエニル基、X4は陰イオン(塩素、
臭素、沃素、硫酸、スルホン酸、メチル硫酸、リン酸、
硝酸等)、pは1〜50の整数、qは0〜50の整数、
rは150〜8000の整数を示す。本発明で用いられ
るジアリル4級アンモニウム塩/アクリルアミド共重合
物の分子量としては約3万〜200万が好ましく、更に
好ましくは10万〜100万の範囲である。市販品とし
ては、メルコ社のマーコート100,550,280な
どが挙げられる。
[Chemical 7] In formulas (6) and (7), R18 and R19 are the same or different, and are hydrogen, an alkyl group (having 1 to 18 carbon atoms), a phenyl group, an aryl group, a hydroxyalkyl group, an amidoalkyl group, a cyanoalkyl group. , Alkoxyalkyl groups, or carboalkoxyalkyl groups R20, R21, R22, R23
Are the same or different, hydrogen, a lower alkyl group (having 1 to 3 carbon atoms) or a phenyl group, X4 is an anion (chlorine,
Bromine, iodine, sulfuric acid, sulfonic acid, methyl sulfuric acid, phosphoric acid,
Nitric acid), p is an integer of 1 to 50, q is an integer of 0 to 50,
r represents an integer of 150 to 8000. The molecular weight of the diallyl quaternary ammonium salt / acrylamide copolymer used in the present invention is preferably about 30,000 to 2,000,000, more preferably 100,000 to 1,000,000. Examples of commercially available products include Mercote 100, 550 and 280 manufactured by Melco.

【0015】4級化ポリビニルピロリドン誘導体として
は次式(8)で示されるものが好ましい。
The quaternized polyvinylpyrrolidone derivative is preferably represented by the following formula (8).

【0016】[0016]

【化8】 式(8)中、R24は水素原子または炭素数1〜3のアル
キル基、R25,R26,R27は同じかまたは異なってお
り、水素原子、炭素数1〜4のアルキル基、ヒドロキシ
アルキル基、アミドアルキル基、シアノアルキル基、ア
ルコキシアルキル基またはカルボアルコキシアルキル
基、Y1は酸素原子またはアミド結合中のNH基、X5は
陰イオン(塩素、臭素、沃素、硫酸、スルホン酸、炭素
数1〜4のアルキル硫酸、リン酸、硝酸等)、uは1〜
10の整数、s+t=20〜8000の整数を示す。本
発明で用いられる4級化ポリビニルピロリドン誘導体の
分子量としては1万〜200万が好ましく、更に好まし
くは5万〜150万である。市販品としては、ガフ社の
ガフコート734,755,755N等が挙げられる。
[Chemical 8] In formula (8), R24 is a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, R25, R26 and R27 are the same or different, and a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, a hydroxyalkyl group, an amide Alkyl group, cyanoalkyl group, alkoxyalkyl group or carboalkoxyalkyl group, Y1 is an oxygen atom or an NH group in an amide bond, X5 is an anion (chlorine, bromine, iodine, sulfuric acid, sulfonic acid, having 1 to 4 carbon atoms) Alkylsulfuric acid, phosphoric acid, nitric acid, etc., u is 1 to
An integer of 10 and an integer of s + t = 20 to 8000 are shown. The molecular weight of the quaternized polyvinylpyrrolidone derivative used in the present invention is preferably 10,000 to 2,000,000, more preferably 50,000 to 1,500,000. Examples of commercially available products include Guff Coat 734, 755, 755N manufactured by Gaff.

【0017】これらの中でもカチオン化セルロース誘導
体およびジアリル4級アンモニウム塩/アクリルアミド
共重合物が好ましい。その配合量は、0.01〜5重量
%が好ましく、更に好ましくは0.1〜3重量%であ
る。
Of these, cationized cellulose derivatives and diallyl quaternary ammonium salt / acrylamide copolymers are preferred. The blending amount is preferably 0.01 to 5% by weight, more preferably 0.1 to 3% by weight.

【0018】本発明の染毛剤組成物は、下記の通常の染
毛剤組成物に配合されるものも含まれる。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、ジアミノジフェニルアミ
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、「医薬部外品原料規格」(19
91年6月発行,薬事日報社)に収載されたものを用い
ることができる。更に、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、ポリオキ
シエチレンアルキルエーテル等の界面活性剤、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、脂肪酸、紫外線吸収剤、防腐剤、パール剤、可溶化
剤、浸透剤、湿潤剤、色素、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、酸化剤としては、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、染毛処理の直前に染毛剤組成物と酸化剤とを
混合して染毛液を調製し、毛髪に塗布する。尚、染毛剤
組成物の剤型はクリーム、ゲル、ペーストなど粘稠な型
態である方が、染毛時の毛髪への付着性がよく、染色性
および堅牢性の点で好ましい。また、染毛液を塗布した
後の放置時間を5〜15分程度に短縮することもできる
という利点もある。
The hair dye composition of the present invention includes those which are blended with the following usual hair dye compositions. As the oxidative dye intermediate, phenylenediamines, aminophenols, toluylenediamines, aminonitrophenols, diphenylamines, diaminodiphenylamines, N-phenylphenylenediamines, diaminopyridines and the like and salts thereof are usually used. 1 type (s) or 2 or more types are mentioned. The blending amount is, for example, about 0.01 to 10% by weight based on the total weight of the first agent. Further, resorcin, pyrogallol, catechol, metaaminophenol, metaphenylenediamine and the like can be blended as a coupler. In addition, "Standards for Quasi-drug Raw Materials" (19
Those listed in Yakuji Nippo (published in June 1991) can be used. Furthermore, moisturizers such as glycerin and propylene glycol, oily ingredients such as lanolin, squalane and liquid paraffin, stabilizers such as sulfite and ascorbic acid, thickeners such as carboxymethyl cellulose, and surfactants such as polyoxyethylene alkyl ether. , Ammonia, alkali agents such as alkanolamines, higher alcohols, fatty acids, ultraviolet absorbers, preservatives, pearlizing agents, solubilizers, penetrants, wetting agents, dyes, fragrances, etc. may be appropriately added as necessary. it can. On the other hand, the oxidizing agent contains hydrogen peroxide, an oxidizing agent such as urea peroxide, phenacetin, a stabilizer such as EDTA, a surfactant, oils and fats,
Higher alcohols, acids, pH adjusters, fragrances and the like can be appropriately added as needed. When this hair dye is used, the hair dye composition is mixed with an oxidizing agent immediately before the hair dyeing treatment to prepare a hair dye solution, which is applied to the hair. It is preferable that the hair dye composition has a viscous form such as cream, gel, or paste in terms of good adhesion to hair during hair dyeing and dyeability and fastness. Further, there is an advantage that the standing time after applying the hair dye can be shortened to about 5 to 15 minutes.

【0019】以下実施例を挙げて更に詳細に説明する。Hereinafter, the present invention will be described in more detail with reference to examples.

【0020】[0020]

【実施例】表1に示す実施例1および比較例1〜3を調
整し、下記の染毛試験および安定性試験を行い、その結
果を表1に示した。
EXAMPLES Example 1 and Comparative Examples 1 to 3 shown in Table 1 were prepared and subjected to the following hair dyeing test and stability test, and the results are shown in Table 1.

【0021】[0021]

【表1】 上記実施例1および比例例1〜3について以下に示す方
法で染毛試験および安定性試験を行った。なお、酸化剤
としては6%過酸化水素水溶液を用いた。
[Table 1] A hair dyeing test and a stability test were performed on the above-mentioned Example 1 and the proportional examples 1 to 3 by the methods described below. A 6% aqueous hydrogen peroxide solution was used as the oxidizing agent.

【0022】<酸化剤> 35%過酸化水素水17.0重量% 精製水で100%にする<Oxidizing agent> 35% hydrogen peroxide solution 17.0% by weight Purified water to 100%

【0023】(1)染毛試験 実施例1及び比較例1〜3の染毛剤組成物を前記の酸化
剤と1対1の割合で混合し、人毛白髪の毛束に塗布し室
温で10分間放置後、シャンプーし、すすぎ乾燥した。
そして、染色毛の肉眼評価及び官能評価を下記の基準に
より行った。 評価基準 ◎:極めて良好 ○:良好 △:やや不良 ×:不良
(1) Hair Dyeing Test The hair dye compositions of Example 1 and Comparative Examples 1 to 3 were mixed with the above-mentioned oxidizing agent in a ratio of 1: 1 and applied to a hair bundle of human white hair at room temperature for 10 minutes. After leaving for a minute, it was shampooed, rinsed and dried.
Then, the naked eye evaluation and the sensory evaluation of the dyed hair were performed according to the following criteria. Evaluation criteria ◎: Very good ○: Good △: Somewhat bad ×: Bad

【0024】(2)安定性試験 実施例1及び比較例1〜3の染毛剤組成物を50℃で1
ケ月保存し、安定性、粘度の変化、2剤との混合性を下
記の基準により評価し、その結果を表1に示した。 ◎:極めて良好 ○:良好 △:やや不良 ×:不良
(2) Stability Test The hair dye compositions of Example 1 and Comparative Examples 1 to 3 were subjected to 1 at 50 ° C.
After storage for a month, stability, change in viscosity, and compatibility with two agents were evaluated according to the following criteria, and the results are shown in Table 1. ◎: Very good ○: Good △: Slightly bad ×: Bad

【0025】 実施例2 重量% セチルアルコール 3.0 パラフィン130゜F 3.0 ポリオキシエチレン(2)オレイルエーテル 5.0 ポリオキシエチレン(20)オレイルエーテル 5.0 ラウリル硫酸ナトリウム 1.0 プロモイスEUP※1 1.0 マーコート550※2 0.5 p−フェニレンジアミン 1.5 レゾルシン 1.0 m−アミノフェノール 0.5 28%アンモニア水 3.0 精製水で100%とする ※1 ウンデシレノイル加水分解コラーゲンカリウム
((株)成和化成) ※2 塩化ジメチルジアリルアンモニウム・アクリルア
ミド共重合体液((株)松本交商) 上記組成のクリーム状染毛剤組成物を調整し、実施例1
の酸化剤と混合した染毛液を白髪混じりの毛束に塗布
し、15分放置した後、シャンプーで洗浄すると、実施
例1と同様に染め上がりが良好で、毛髪の感触にも優れ
た結果が得られた。
Example 2 Weight% Cetyl Alcohol 3.0 Paraffin 130 ° F 3.0 Polyoxyethylene (2) oleyl ether 5.0 Polyoxyethylene (20) oleyl ether 5.0 Sodium lauryl sulphate 1.0 Promois EUP * 1 1.0 Marquat 550 * 2 0.5 p-phenylenediamine 1.5 resorcin 1.0 m-aminophenol 0.5 28% ammonia water 3.0 3.0% with purified water * 1 undecylenoyl hydrolyzed collagen Potassium (Sowa Kasei Co., Ltd.) * 2 Dimethyldiallylammonium chloride / acrylamide copolymer liquid (Matsumoto Trading Co., Ltd.) A cream hair dye composition having the above composition was prepared, and Example 1 was prepared.
When the hair dye mixed with the oxidizing agent is applied to a hair bundle containing white hair, left for 15 minutes, and washed with shampoo, the dyeing is good as in Example 1, and the feel of the hair is excellent. Was obtained.

【0026】 実施例3 重量% ステアリルアルコール 5.0 ワセリン 2.0 ポリオキシエチレン・ポリオキシプロピレンセチルエーテル 8.0 ラウリル硫酸ナトリウム 1.0 プロモイスECT※1 1.0 セルコートL−200※2 0.5 p−フェニレンジアミン 1.0 レゾルシン 0.5 o−アミノフェノール 0.5 モノエタノールアミン 2.0 精製水で100%する ※1 ヤシ油脂肪酸加水分解コラーゲントリエタノール
アミン ※2 ヒドロキシエチルセルロースジメチルジアリルア
ンモニウムクロリド 上記組成のクリーム状染毛剤組成物を調整し、実施例1
の酸化剤と混合した染毛液を白髪混じりの毛束に塗布
し、10分放置した後、シャンプーで洗浄すると、実施
例1と同様に染め上がりが良好で、毛髪の感触にも優れ
た結果が得られた。
Example 3 Weight% Stearyl alcohol 5.0 Vaseline 2.0 Polyoxyethylene / polyoxypropylene cetyl ether 8.0 Sodium lauryl sulfate 1.0 Promote ECT * 1 1.0 Cell coat L-200 * 2 0. 5 p-Phenylenediamine 1.0 Resorcinol 0.5 o-Aminophenol 0.5 Monoethanolamine 2.0 100% with purified water * 1 Coconut oil fatty acid hydrolyzed collagen triethanolamine * 2 Hydroxyethylcellulose dimethyldiallylammonium chloride A creamy hair dye composition having the above composition was prepared, and Example 1
When the hair dye mixed with the oxidizing agent is applied to a hair bundle containing white hair, and the hair bundle is left for 10 minutes and washed with shampoo, the dyeing is good as in Example 1, and the feel of the hair is excellent. Was obtained.

【0027】 実施例4 重量% セトステアリルアルコール 3.0 ラノリン 1.0 ポリオキシエチレン(10)ベヘニルエーテル 5.0 ポリオキシエチレン(30)ベヘニルエーテル 5.0 グリセリン 5.0 ラウリル硫酸ナトリウム 1.0 p−フェニレンジアミン 1.0 レゾルシン 1.0 p−アミノフェノール 1.0 28%アンモニア水 4.0 ニッコールCCN−40※1 1.0 マーコート100※2 0.5 ※1 ヤシ油脂肪酸加水分解コラーゲンナトリウム液
((株)日光ケミカル) ※2 ジメチルジアリルアンモニウムクロライド
((株)松本交商) 上記組成のクリーム状染毛剤組成物を調整し、実施例1
の酸化剤と混合した染毛液を白髪混じりの毛束に塗布
し、10分放置した後、シャンプーで洗浄すると、実施
例1と同様に染め上がりが良好で、毛髪の感触にも優れ
た結果が得られた。
Example 4 wt% cetostearyl alcohol 3.0 lanolin 1.0 polyoxyethylene (10) behenyl ether 5.0 polyoxyethylene (30) behenyl ether 5.0 glycerin 5.0 sodium lauryl sulphate 1.0 p-phenylenediamine 1.0 resorcin 1.0 p-aminophenol 1.0 28% ammonia water 4.0 Nikkor CCN-40 * 1 1.0 Marquat 100 * 2 0.5 * 1 sodium coconut oil fatty acid hydrolyzed collagen sodium Liquid (Nikko Chemical Co., Ltd.) * 2 Dimethyldiallylammonium chloride (Matsumoto Trading Co., Ltd.) A cream hair dye composition having the above composition was prepared, and Example 1 was prepared.
When the hair dye mixed with the oxidizing agent is applied to a hair bundle containing white hair, and the hair bundle is left for 10 minutes and washed with shampoo, the dyeing is good as in Example 1, and the feel of the hair is excellent. Was obtained.

【0028】[0028]

【発明の効果】安定性が良好で、1剤と2剤の混合が容
易であり、しかも染め上がりが良好でかつ染毛後の毛髪
の感触にも優れる。
EFFECT OF THE INVENTION The stability is good, the one agent and the second agent can be easily mixed, the dyeing is good, and the feel of the hair after dyeing is excellent.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 アシル化コラーゲンポリペプタイド及び
カチオン化ポリマーを含むことを特徴とする染毛剤組成
物。
1. A hair dye composition comprising an acylated collagen polypeptide and a cationized polymer.
JP18936693A 1993-06-30 1993-06-30 Hair dye composition Expired - Fee Related JP2872888B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18936693A JP2872888B2 (en) 1993-06-30 1993-06-30 Hair dye composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18936693A JP2872888B2 (en) 1993-06-30 1993-06-30 Hair dye composition

Publications (2)

Publication Number Publication Date
JPH0717836A true JPH0717836A (en) 1995-01-20
JP2872888B2 JP2872888B2 (en) 1999-03-24

Family

ID=16240121

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18936693A Expired - Fee Related JP2872888B2 (en) 1993-06-30 1993-06-30 Hair dye composition

Country Status (1)

Country Link
JP (1) JP2872888B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0940534A (en) * 1995-07-27 1997-02-10 Shiseido Co Ltd Hair dye composition of type mixed on employment
JP2002338443A (en) * 2001-05-23 2002-11-27 Kanebo Ltd Hair dye or bleaching agent composition
JP2005089307A (en) * 2003-09-12 2005-04-07 Hoyu Co Ltd Hair cosmetic composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0940534A (en) * 1995-07-27 1997-02-10 Shiseido Co Ltd Hair dye composition of type mixed on employment
JP2002338443A (en) * 2001-05-23 2002-11-27 Kanebo Ltd Hair dye or bleaching agent composition
JP2005089307A (en) * 2003-09-12 2005-04-07 Hoyu Co Ltd Hair cosmetic composition

Also Published As

Publication number Publication date
JP2872888B2 (en) 1999-03-24

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