JPH02115114A - Powdery oxidation hair dye - Google Patents

Powdery oxidation hair dye

Info

Publication number
JPH02115114A
JPH02115114A JP63269204A JP26920488A JPH02115114A JP H02115114 A JPH02115114 A JP H02115114A JP 63269204 A JP63269204 A JP 63269204A JP 26920488 A JP26920488 A JP 26920488A JP H02115114 A JPH02115114 A JP H02115114A
Authority
JP
Japan
Prior art keywords
hair dye
hair
dye
polypeptide
cellulose ether
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
JP63269204A
Other languages
Japanese (ja)
Other versions
JPH044291B2 (en
Inventor
Toshihiko Yamamoto
敏彦 山本
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
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 Hoyu Co Ltd filed Critical Hoyu Co Ltd
Priority to JP63269204A priority Critical patent/JPH02115114A/en
Publication of JPH02115114A publication Critical patent/JPH02115114A/en
Publication of JPH044291B2 publication Critical patent/JPH044291B2/ja
Granted legal-status Critical Current

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  • Coloring (AREA)

Abstract

PURPOSE:To obtain a powdery oxidation hair dye, excellent in fluidity when dissolved in water for use, further fastness and finishing of hair after dyeing thereof by blending a quaternary nitrogen-containing cellulose ether and a polypeptide with other ingredients. CONSTITUTION:The objective substance obtained by blending a well-known powder oxidation hair dye with a quaternary nitrogen-containing cellulose ether and a polypeptide and preparing a hair dye. Polymer JR-125(R) manufactured by Union Carbide Corp., etc., are exemplified as the quaternary nitrogen- containing cellulose ether and the amount thereof blended is 0.1-20wt.% based on the hair dye. Promois W-42CP(R) manufactured by Seiwa Kasei Co., Ltd., etc., are exemplified as the polypeptide and the amount thereof blended is 0.1-20wt.% based on the hair dye. If the powdery oxidation hair dye is used, the hair dye is dissolved in a solution, such as water, so as to provide 8-25wt.% content thereof according to a conventional method to prepare a pasty hair dye solution, which is then applied to hair using a comb, brush or hand.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は粉末酸化染毛剤に関するもので、詳しくは、使
用時に水に溶解した場合の流動特性が優れている上、染
毛後における堅牢性及び毛髪の仕上りに優れた粉末酸化
染毛剤に関するものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a powdered oxidation hair dye, and more specifically, it has excellent flow characteristics when dissolved in water during use, and has good durability after hair dyeing. This invention relates to a powdered oxidative hair dye with excellent properties and hair finish.

[従来技術とその問題点] 粉末酸化染毛剤としては、通常、粉末状の酸化染料と粉
末状の酸化剤とを混合して一包として、使用直前に液剤
を加えて染毛液を調製する一剤型、粉末状の酸化染料と
粉末状の酸化剤を分包した二剤型、粉末状の酸化染料を
一包とし、液状の酸化剤とを使用直前に混合し染毛液を
調製する二剤型の粉末染毛剤が知られている。これら粉
末状酸化染毛剤はいずれも、粉末状であることから、’
Ha管理及び輸送が容易であること、使用方法が簡便で
小分使用ができること、軽量で携帯に便利であることな
どの利点を有するため、ある面では液体式染毛剤よりも
要望性の高いものでおる。粉末酸化染毛剤を使用する場
合には、使用直前に水、温湯又は適当な希釈液等に溶か
して粘稠なペースト状の染毛液を調製し、これをへケや
ブラシ、手などにより頭髪に塗布する必要があるが、こ
の場合、染毛液は適度の粘度を有することが望ましい。
[Prior art and its problems] Powdered oxidation hair dyes are usually prepared by mixing a powdered oxidation dye and a powdered oxidizing agent into a package, and adding a liquid agent just before use to prepare a hair dye solution. A one-dose type, a two-dose type that contains a powdered oxidation dye and a powdered oxidizing agent, and a two-dose type that contains a powdered oxidized dye and a liquid oxidizing agent and mixes it immediately before use to prepare a hair dye solution. Two-component powder hair dyes are known. Since all of these powdered oxidation hair dyes are in powder form,
In some respects, it is more desirable than liquid hair dye because it has the advantages of being easy to manage and transport, easy to use and can be used in small doses, and lightweight and convenient to carry. It's something. When using powdered oxidation hair dye, dissolve it in water, warm water, or an appropriate diluent immediately before use to prepare a viscous paste-like hair dye, and then apply it with a brush, brush, or hand. It is necessary to apply it to the hair, but in this case it is desirable that the hair dye has an appropriate viscosity.

そのため、従来、染毛液の粘度を調整するために、例え
ば、デンプンなどの天然高分子、カルボキシメチルセル
ロースなどの半合成高分子、ポリビニルアルコールなど
の合成高分子を配合する方法が採用されている。
Therefore, conventionally, in order to adjust the viscosity of hair dye solutions, methods have been adopted in which, for example, natural polymers such as starch, semi-synthetic polymers such as carboxymethyl cellulose, and synthetic polymers such as polyvinyl alcohol are blended.

ところが、この方法の場合、染毛液の施用時の粘度は適
当に調節できるものの、粉末酸化染毛剤を水などに最初
に溶解する際の粘度も高くなり、粉末成分を均一に溶解
することが難しいと言う欠点を有する。一方、溶解初期
における溶解性を良くすれば、当然のことながら、施用
時の粘度も低く、染毛中や染毛処理後に毛髪から染毛液
が垂れ落ち、皮膚や地肌を汚染するという欠点がある。
However, in this method, although the viscosity of the hair dye solution when applied can be adjusted appropriately, the viscosity when the powdered oxidized hair dye is first dissolved in water etc. also becomes high, making it difficult to dissolve the powder components uniformly. The disadvantage is that it is difficult to On the other hand, if the solubility at the initial stage of dissolution is improved, the viscosity at the time of application will be low, and the disadvantage is that the hair dye solution will drip from the hair during hair dyeing or after the hair dyeing process, contaminating the skin and scalp. be.

また、粉末酸化染毛剤においても、染毛後の堅牢性がよ
り優れ、しかも、毛髪の仕上りが良好なものが要求され
ている。
Powdered oxidation hair dyes are also required to have better fastness after dyeing and to give a good finish to the hair.

[発明の課題と解決手段] 本発明者は上記実情に鑑み、粉末成分を水などに簡単に
均一溶解することができ、しかも、施用時には染毛液が
適度な粘性を有する粉末酸化染毛剤を得るべく鋭意検討
した結果、第4級窒素含有セルロースエーテル及びポリ
ペプタイドとを配合することにより、溶解初期における
粘度は低く粉末成分を均一溶解させることができる上、
その後、徐々に染毛液の粘度が上昇し、施工時には適度
な粘性が得られることを見い出し本発明を完成した。
[Problems to be solved by the invention and means for solving the problem] In view of the above circumstances, the present inventor has developed a powdered oxidation hair dye in which the powder component can be easily and uniformly dissolved in water etc., and the hair dye solution has an appropriate viscosity when applied. As a result of intensive studies to obtain this, we found that by blending quaternary nitrogen-containing cellulose ether and polypeptide, the viscosity at the initial stage of dissolution is low, and the powder components can be uniformly dissolved.
Thereafter, they discovered that the viscosity of the hair dye solution gradually increased and that appropriate viscosity could be obtained during application, and the present invention was completed.

要するに、本発明の場合、均一溶解された適度な粘性の
染毛液を用いて染毛処理ができるため、伸展性、易塗布
性、均染性及び垂れ正性に優れ、また、ポリペプタイド
が毛髪の損傷部位に浸透・吸着し、更に第4級窒素含有
セルロースエーテルが毛髪表面に被膜を形成するために
、毛髪内部に浸透した色素を良好に保持するので優れた
堅牢性を有するという効果もある。
In short, in the case of the present invention, hair can be dyed using a uniformly dissolved hair dye solution with an appropriate viscosity, so it has excellent spreadability, easy application, level dyeing, and straightness of sagging, and the polypeptide is It penetrates and adsorbs into the damaged areas of the hair, and since the quaternary nitrogen-containing cellulose ether forms a film on the hair surface, it retains the pigment that has penetrated into the hair well, resulting in excellent fastness. be.

すなわち、本発明の要旨は、第4級窒素含有セルロース
エーテル及びポリペプタイドを配合したことを特徴とす
る粉末酸化染毛剤に存する。
That is, the gist of the present invention resides in a powdered oxidative hair dye characterized by containing a quaternary nitrogen-containing cellulose ether and a polypeptide.

以下、本発明の詳細な説明する。The present invention will be explained in detail below.

本発明で対象とする粉末酸化染毛剤としては、通常、粉
末状の酸化染料と粉末状の酸化剤とを混合して一包とし
た一剤型、あるいは分包とした二剤型、更に、酸化剤は
液状であるものの酸化染料を含む第−剤のみが粉末状の
ものなどが挙げられる。
The powdered oxidation hair dye targeted by the present invention is usually a one-dose type in which a powdered oxidation dye and a powdered oxidizing agent are mixed into one package, or a two-dose type in divided packages; Examples include those in which the oxidizing agent is in liquid form but only the first agent containing the oxidizing dye is in powder form.

本発明に用いる酸化染毛剤の第1剤の酸化染1!8I中
間体としては、通常、フェニレンジアミン類、アミンフ
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
リジン類等及びそれらの塩類の1種又は2種以上が挙げ
られる。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。更に、「染毛
剤原料規格」 (改訂第三版、昭和60年5月、日本ヘ
アカラー工業会発行)に掲載された化合物を配合しても
よい。これらの染料成分の配合料は通常、全組成物10
0重量部当り0.1〜40重量部の範囲である。
The oxidation dye 1!8I intermediate of the first part of the oxidation hair dye used in the present invention is usually phenylenediamines, aminephenols, tolylenediamines, aminonitrophenols, diphenylamines, diaminophenylamines. , N-phenylphenylenediamines, diaminopyridines, and salts thereof. Furthermore, resorcinol, pyrogallol, catechol, meta-aminophenol, meta-phenylenediamine, etc. can be blended as a coupler. Furthermore, compounds listed in the "Standards for Hair Dye Raw Materials" (revised third edition, May 1985, published by the Japan Hair Color Industry Association) may be blended. The formulation of these dye components is usually 10% of the total composition.
The range is from 0.1 to 40 parts by weight per 0 parts by weight.

一方、酸化剤としては、通常、過硼酸ナトリウム、過酸
化尿素、過酸化メラニン、硫酸ナトリウム・過酸化水素
付加物、ピロ燐酸ナトリウム・過酸化水素付加物、第二
燐酸ナトリウム・過酸化水素付加物、過炭酸ナトリウム
等が挙げられる。
On the other hand, the oxidizing agent is usually sodium perborate, urea peroxide, melanin peroxide, sodium sulfate/hydrogen peroxide adduct, sodium pyrophosphate/hydrogen peroxide adduct, dibasic sodium phosphate/hydrogen peroxide adduct. , sodium percarbonate, and the like.

また、本発明の染毛剤では、染毛液の粘度を調節するた
めに通常、増粘剤が配合されるが、この増粘剤としては
、例えば、デンプン質、海藻類、アルギン酸ナトリウム
、メチルセルロース、ヒドロキシエチルセルローズ、カ
ルボキシメチルセルローズ、ポリビニルアルコール、ポ
リビニルピロリドン、ポリアクリル酸ソーダ、グアーガ
ム、キサンタンガム等が挙げられ、この使用量は通常、
全組成物100重量部に対して5〜40重量部である。
In addition, in the hair dye of the present invention, a thickener is usually added to adjust the viscosity of the hair dye solution, and examples of the thickener include starch, seaweed, sodium alginate, methylcellulose, etc. , hydroxyethyl cellulose, carboxymethyl cellulose, polyvinyl alcohol, polyvinylpyrrolidone, sodium polyacrylate, guar gum, xanthan gum, etc., and the amount used is usually:
The amount is 5 to 40 parts by weight based on 100 parts by weight of the total composition.

本発明の粉末酸化染毛剤はこの他にも適宜の添加剤を配
合することができる。例えば、高級アルキルベンゼンス
ルホン酸塩、脂肪酸石鹸、高級アルキルスルホン酸塩、
高級アルキル燐酸エステル等の界面活性剤、硫酸アンモ
ニウム、硝酸アンモニウム、炭酸アン−Eニウム、塩化
アンモニウム、燐酸第一)7ンー[ニウム、燐酸第二ア
ンモニウム、クエン酸、酒石酸、乳酸、コハク酸等のp
l−1調整剤、炭酸ナトリウム、ケイ酸ナトリウム等の
アルカリ剤などの公知の添加剤を必要に応じて配合して
もよい。
The powdered oxidative hair dye of the present invention may also contain other appropriate additives. For example, higher alkylbenzene sulfonates, fatty acid soaps, higher alkyl sulfonates,
Surfactants such as higher alkyl phosphate esters, ammonium sulfate, ammonium nitrate, ammonium carbonate, ammonium chloride, mono-[nium phosphate, secondary ammonium phosphate, citric acid, tartaric acid, lactic acid, succinic acid, etc.
Known additives such as l-1 regulator, alkali agents such as sodium carbonate and sodium silicate may be blended as necessary.

本発明においては、上述のような粉末酸化染毛剤に第4
級窒素含有セルロースエーテル及びポリペプタイドを配
合することを必須の要件とするものである。すなわち、
この配合剤の作用によって、染毛液の溶解時と施用時の
粘度を適当に調整し、良好な染毛処理ができるのである
In the present invention, a fourth dye is added to the powder oxidation hair dye as described above.
It is an essential requirement to blend a grade nitrogen-containing cellulose ether and a polypeptide. That is,
By the action of this compounding agent, the viscosity of the hair dye solution during dissolution and application can be adjusted appropriately, allowing for a good hair dye treatment.

第4級窒素含有セルロースエーテルとしては、通常、下
記一般式[I]で示される化合物が挙げられる。
Examples of quaternary nitrogen-containing cellulose ethers include compounds represented by the following general formula [I].

(但し、一般式の記号は下記の意味を表わす。)A:ア
ンヒドログルコース単位の残基 Q:50〜20000の整数 1<、−→L、 O←−(C02Cll0汁−→120
)T−11n R,−N−R3・X 1<2 1+ 、  L2 :炭素数2〜3のアルキレン基L3
 :rA素数1〜3のアルキレン基又はヒドロキシアル
キレン基 R1,R2,R3:同−又は異なってもよい炭素数10
までのアルキル基、アリール基、アラルキル基、アルキ
ルアリール基、アルコキシアルキル基又はアルコキシア
リール基であり、これらは何れかの2つが共同して隣接
する窒素原子と共に複素環を形成してもよい。
(However, the symbols in the general formula represent the following meanings.) A: Residue of anhydroglucose unit Q: An integer from 50 to 20,000 1<, -→L, O←-(C02Cll0 juice-→120
)T-11n R, -N-R3.X 1<2 1+ , L2: Alkylene group L3 having 2 to 3 carbon atoms
:rA alkylene group or hydroxyalkylene group with 1 to 3 prime numbers R1, R2, R3: 10 carbon atoms which may be the same or different
is an alkyl group, an aryl group, an aralkyl group, an alkylaryl group, an alkoxyalkyl group, or an alkoxyaryl group, and any two of these may jointly form a heterocycle with the adjacent nitrogen atom.

X:塩素、臭素、ヨウ素、硫酸、スルホン酸、メチル硫
酸、リン酸、酢酸等から選ばれる陰イオンm:0〜10
の整数 n:O〜3の整数 p:O〜10の整数 このカチオン性セルロースXI(本のうち、カチオン化
度、すなわちアンヒドログルコース1単位当りnの平均
値が0.01〜1、特に0.02〜0.5のものが好ま
しい。また、mとpの合計はその平均が1〜3のものが
好ましい。なお、分子量は約100,000〜3,00
0,000の間のものが好ましい。このカチオン性セル
ロース誘導体は例えば、ヒドロキシエチルセルロースと
グリシジルトリメチルアンモニウムクロライドとの反応
により容易に得ることができる。これらの具体例として
は、例えば、ユニオンカーバイド社のポリマーJR−1
25,JR−400,JR−30M、LR−400,L
R−30M、更に、ライオン■のレオガードG、GPな
との市販品を挙げることができる。
X: Anion selected from chlorine, bromine, iodine, sulfuric acid, sulfonic acid, methyl sulfate, phosphoric acid, acetic acid, etc. m: 0 to 10
n: an integer from O to 3 p: an integer from O to 10 This cationic cellulose A value of .02 to 0.5 is preferable.The sum of m and p is preferably an average of 1 to 3.The molecular weight is approximately 100,000 to 3,000.
Those between 0,000 are preferred. This cationic cellulose derivative can be easily obtained, for example, by reacting hydroxyethylcellulose with glycidyltrimethylammonium chloride. Specific examples of these include, for example, Union Carbide's polymer JR-1
25, JR-400, JR-30M, LR-400, L
Commercial products such as R-30M, Lion ■ Leoguard G, and GP can be mentioned.

第4級窒素含有セルロースエーテルの染毛剤への配合量
は通常、0.1〜20重但%が好適であり、特に好まし
くは、0.5〜10重但%でおる。
The amount of the quaternary nitrogen-containing cellulose ether added to the hair dye is usually 0.1 to 20% by weight, particularly preferably 0.5 to 10% by weight.

0.1重足%未満では十分な効果を得ることができず、
20重重旦を越えて配合してもそれ以上の効果は期待で
きない。
If it is less than 0.1%, sufficient effect cannot be obtained.
Even if the amount exceeds 20 kg, no further effect can be expected.

次に、ポリペプタイドとしては、通常、コラーゲン、ケ
ラチン、エラスチン、フィブロイン、コンキオリン、大
豆蛋白、カゼイン等の蛋白質を酸、アルカリ、酵素等に
より加水分解した加水分解物が挙げられる。更に4級化
したカチオン変性蛋白質も利用できる。また、場合によ
っては、上記の蛋白質あるいはその分解物の誘導体、あ
るいは合成ペプチド、天然ペプチドをそのまま使用する
こともできる。これらの具体例としては、コラーゲン加
水分解物の場合、例えば、成用化成■のブロモイスW−
42CP、W−422P、W−52P。
Next, examples of polypeptides include hydrolysates obtained by hydrolyzing proteins such as collagen, keratin, elastin, fibroin, conchiolin, soybean protein, and casein using acids, alkalis, enzymes, and the like. Furthermore, quaternized cationically modified proteins can also be used. In some cases, the above-mentioned proteins or derivatives of their decomposition products, synthetic peptides, and natural peptides can also be used as they are. Specific examples of these include, in the case of collagen hydrolyzate, Bromois W-
42CP, W-422P, W-52P.

W−520P、W−42QP、クローダジャパン側のク
ロティンA、C,Qなど、ケラチン加水分解物の場合、
例えば、成用化成■のブロモイスWK−HP、クローダ
ジャパン■のクロティンHKPなど、エラスチン加水分
解物の場合、例えば、クローダジャバン■のクロラスチ
ンパウダーなど、フィブロイン加水分解物の場合、例え
ば、成用化成■のブロモイスシルク−1000P、−丸
ファルス■のシルクゲンGパウダーなどの各々の市販品
を挙げることができる。
In the case of keratin hydrolysates such as W-520P, W-42QP, Crotin A, C, and Q from Croda Japan,
For example, in the case of elastin hydrolyzate such as Seiyo Kasei's Bromois WK-HP and Croda Japan ■'s Clotin HKP, for example, in the case of fibroin hydrolyzate such as Cloda Japan's chlorastine powder, for example, Seiyo Kasei's Examples of commercially available products include Bromois Silk-1000P (1) and Silk Gen G Powder (2).

ポリペプタイドの染毛剤への配合量は0.1〜20重量
%が好適であり、特に好ましくは、0゜5〜10重猷%
である。0.1重量%未満では十分な効果を得ることが
できず、20重n%を越えて配合してもそれ以上の効果
は期待できない。
The amount of polypeptide added to the hair dye is preferably 0.1 to 20% by weight, particularly preferably 0.5 to 10% by weight.
It is. If it is less than 0.1% by weight, sufficient effects cannot be obtained, and even if it exceeds 20% by weight, no further effects can be expected.

本発明の粉末酸化染毛剤を使用する場合は、常法に従っ
て、水などの液剤に8.0〜25.0重量%となるよう
に溶いてペースト状の染毛液を調製し、これをクシ、ブ
ラシあるいは手で頭髪に塗布する。
When using the powdered oxidation hair dye of the present invention, prepare a paste-like hair dye by dissolving it in a liquid such as water to a concentration of 8.0 to 25.0% by weight according to a conventional method. Apply to hair with comb, brush or hands.

[発明の効果] 本発明の粉末酸化染毛剤によれば、第4級窒素含有セル
ロースエーテルとポリペプタイドの相互作用により、溶
解初期における染毛液の粘度はあまり高くないため、粉
末成分を簡単に均一溶解できる上、施用時には適度な粘
度となるので施用時にお【プる問題がなく、しかも、染
毛後における堅牢性並びに毛髪の仕上りに優れている。
[Effects of the Invention] According to the powdered oxidative hair dye of the present invention, the viscosity of the hair dye solution at the initial stage of dissolution is not very high due to the interaction between the quaternary nitrogen-containing cellulose ether and the polypeptide, so the powder components can be easily mixed. It can be uniformly dissolved in the hair, and has a suitable viscosity when applied, so there is no problem of dripping during application, and it also has excellent fastness and hair finish after dyeing.

(実施例) 次に、本発明を実施例により更に詳細に説明するが、本
発明はその要旨を超えない限り、以下の実施例の記述に
限定されるものではない。
(Examples) Next, the present invention will be explained in more detail with reference to examples, but the present invention is not limited to the description of the following examples unless it exceeds the gist thereof.

実施例1〜3及び比較例1〜3 第1表に示す各成分を均一に混合した粉末酸化染毛剤を
各々、調製し、各染毛剤20gを水100dに溶解した
ものを染毛液とし、これを白髪に塗布し常温で20分間
放置した後、次いで、シャンプーを用いて洗浄すること
により染毛処理を行なった。
Examples 1 to 3 and Comparative Examples 1 to 3 Powder oxidation hair dyes were prepared by uniformly mixing each component shown in Table 1, and 20 g of each hair dye was dissolved in 100 d of water to form a hair dye solution. After applying this to gray hair and leaving it for 20 minutes at room temperature, the hair was dyed by washing with shampoo.

この染毛処理を10名のパネラ−により実施した場合の
各染毛剤の評価結果を下記に示す。
The evaluation results of each hair dye when this hair dyeing treatment was carried out by 10 panelists are shown below.

[パネラ−テストの評価結果コ (1)流動特性(初期溶解性) く単位=名〉 (2)伸展性・易塗布性 (3)垂れ正性・粘度安定性 (4)均染性 (5)堅牢性 ■耐シャンプー性 染色毛をラウリル硫酸ナトリウム10%水溶液で2回シ
センプーし、次に、乾燥する操作を30回繰返し、該処
理を行なわない染色毛を対照として下記の基準で比較し
た。
[Evaluation results of panel test (1) Flow characteristics (initial solubility) unit = name> (2) Spreadability/Easy application (3) Sagging property/Viscosity stability (4) Level dyeing property (5) ) Fastness - Shampoo resistance The dyed hair was soaked twice with a 10% sodium lauryl sulfate aqueous solution and then dried 30 times, and the dyed hair without the treatment was compared using the following criteria as a control.

■耐光性 染色毛を日光に60日間曝露し、該処理を行なわない染
色毛を対照として下記のg i(1;で比較した。
(2) Light resistance Dyed hair was exposed to sunlight for 60 days and compared using the following g i (1;) with dyed hair that was not subjected to the treatment as a control.

実施例4 第4級窒素含有セルロースエーテル 2.0重足% エラスチン加水分解物     8.0 !/パラフェ
ニレンジアミン    2.0 !/メタアミノフェノ
ール     0,3 〃塩酸メタフェニレンジアミン
  0.1 〃レゾルシン          0.5
 !lビロリン酸ナトリウム・過酸化水素付加物30 
〃 ケイ酸す1〜リウム      20 〃カルボキシメ
チル う1クリル硫酸すトリウム    3  1/香料  
           0.1 〃上記粉末染毛剤20
gを水100威に溶かし染毛液を調製し、これを白髪の
混った毛髪に塗布し、30分放置後、シャンプーし乾燥
させたところ、均一に混合された染毛液が調製でき、し
かも、毛髪は自然な黒色に良好に染毛された。
Example 4 Quaternary nitrogen-containing cellulose ether 2.0% elastin hydrolyzate 8.0! /Paraphenylenediamine 2.0! /Meta-aminophenol 0.3 〃Meta-phenylenediamine hydrochloride 0.1 〃Resorcinol 0.5
! l Sodium birophosphate/hydrogen peroxide adduct 30
〃 Sourium silicate 20 〃 Carboxymethyl chloride Sodium sulfate 3 1/Fragrance
0.1 〃Above powder hair dye 20
g in 100 parts water to prepare a hair dye solution, apply this to hair mixed with gray hair, leave it for 30 minutes, shampoo and dry, a uniformly mixed hair dye solution can be prepared, Moreover, the hair was well dyed to a natural black color.

実施例5 第4級窒素含有セルロースエーテル 7、0重量% コンキオリン加水分解物    1.O 〃パラトルイ
レンジアミン    2.O 〃メタアミノフェノール
     0.3IIレゾルシン          
0.6 〃過酸化メラミン       35 〃カル
ボキシメチルセルロース 20 〃炭酸アンモニウム 
      6 〃炭酸ナトリウム       20
 〃ラウリル硫酸ナトリウム    8 〃香料   
          0.1 〃実施例4と同様に行な
ったところ、明るい自然な栗色に染毛された。
Example 5 Quaternary nitrogen-containing cellulose ether 7, 0% by weight Conchiolin hydrolyzate 1. O Paratoluylene diamine 2. O Meta-aminophenol 0.3II resorcinol
0.6 〃Melamine peroxide 35 〃Carboxymethyl cellulose 20 〃Ammonium carbonate
6 Sodium carbonate 20
〃Sodium lauryl sulfate 8 〃Fragrance
0.1 When the same procedure as in Example 4 was carried out, the hair was dyed a bright natural chestnut color.

実施例6〜7 実施例5の粉末染毛剤において、コンキオリン加水分解
物の代わりに、大豆蛋白加水分解物あるいはカゼイン加
水分解物を配合すると同様の良好な結果を得ることがで
きた。
Examples 6 to 7 In the powder hair dye of Example 5, similar good results could be obtained by blending soybean protein hydrolyzate or casein hydrolyzate instead of conchiolin hydrolyzate.

Claims (1)

【特許請求の範囲】[Claims] (1)第4級窒素含有セルロースエーテル及びポリペプ
タイドを配合したことを特徴とする粉末酸化染毛剤。
(1) A powdered oxidative hair dye characterized by containing a quaternary nitrogen-containing cellulose ether and a polypeptide.
JP63269204A 1988-10-25 1988-10-25 Powdery oxidation hair dye Granted JPH02115114A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63269204A JPH02115114A (en) 1988-10-25 1988-10-25 Powdery oxidation hair dye

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63269204A JPH02115114A (en) 1988-10-25 1988-10-25 Powdery oxidation hair dye

Publications (2)

Publication Number Publication Date
JPH02115114A true JPH02115114A (en) 1990-04-27
JPH044291B2 JPH044291B2 (en) 1992-01-27

Family

ID=17469123

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63269204A Granted JPH02115114A (en) 1988-10-25 1988-10-25 Powdery oxidation hair dye

Country Status (1)

Country Link
JP (1) JPH02115114A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002308744A (en) * 2001-04-05 2002-10-23 Dongsung Pharm Co Ltd Composition for hairdye

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002308744A (en) * 2001-04-05 2002-10-23 Dongsung Pharm Co Ltd Composition for hairdye

Also Published As

Publication number Publication date
JPH044291B2 (en) 1992-01-27

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