JPS5835106A - First solution for hair dyeing - Google Patents

First solution for hair dyeing

Info

Publication number
JPS5835106A
JPS5835106A JP13270781A JP13270781A JPS5835106A JP S5835106 A JPS5835106 A JP S5835106A JP 13270781 A JP13270781 A JP 13270781A JP 13270781 A JP13270781 A JP 13270781A JP S5835106 A JPS5835106 A JP S5835106A
Authority
JP
Japan
Prior art keywords
guanidine
solution
hair
alkali
agent
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
JP13270781A
Other languages
Japanese (ja)
Other versions
JPH0231690B2 (en
Inventor
Katsumi Mizumaki
水牧 勝美
Junichi Fujiwara
藤原 順一
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.)
Kashiwa Kagaku Kogyo KK
Original Assignee
Kashiwa Kagaku Kogyo KK
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 Kashiwa Kagaku Kogyo KK filed Critical Kashiwa Kagaku Kogyo KK
Priority to JP13270781A priority Critical patent/JPS5835106A/en
Publication of JPS5835106A publication Critical patent/JPS5835106A/en
Publication of JPH0231690B2 publication Critical patent/JPH0231690B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:The first solution for hair dyeing in which a basic salt of guanidine such as guanidine hydroxide or guanidine carbonate is used as an alkali component to regulate its pH and the consumption of N/10 standard acid solution in specified ranges respectively. CONSTITUTION:The objective first solution for hair dyeing contains as the alkali component at least one selected from guanidine hydroxide, guanidine carbonate, guanidine bicarbonate, guanidine phosphate, guanidine borate and guanidine organic acid salts and so its shows a pH of 8.5-10.5 and consumes N/10 standard acid solution by 5-35ml/g. When ammonia is used as the alkali component, it is preferred because it is volatile. However, attention should be paid its odor and the objective solution may contain less than 0.8wt% NH3, when the consumption of N/10 standard acid solution is 5-35ml/g.

Description

【発明の詳細な説明】 本発明は、しらが染ならびにおしやれ染等に用いられる
、バラフェニレンジアミンを代表してその類似体を総称
する酸化染料を含有する第】剤と、過酸化水素等の酸化
剤を含有する第2剤とを組合せる染毛剤において、その
うち第1剤についての改良に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a first agent containing an oxidation dye representing phenylene diamine and generically referring to its analogues, which is used for Shiraga dyeing, Oshiyare dyeing, etc., and hydrogen peroxide. This invention relates to improvements in the first agent in hair dyes that are combined with a second agent containing an oxidizing agent such as the above.

この種の染毛剤には粉末式、液状式、ンヤンプ一式、ク
リーム式と種々あるが、その殆んどの第1剤はアルカリ
性となっている。
There are various types of hair dyes of this type, such as powder type, liquid type, dyestuff type, and cream type, but the first agent of most of them is alkaline.

このアルカ リについて従来アンモニア水が主 −に使
われていた。アンモニアは毛髪を膨潤させ作用も温和で
望ましいアルカリ薬剤であるが、残念乍ら揮発性のため
その臭気が嫌われるのである。
Conventionally, ammonia water was mainly used as the alkali. Ammonia is a desirable alkaline agent because it swells the hair and has a mild action, but unfortunately its odor is disliked due to its volatility.

これに対しKO)T 、 Na2CO3の様な無機アル
カリは毛髪に残存し易く毛髪?傷う原因となるので、p
Hをあげる場合にのみ少量用いる匠限られる。近年()
 !I ) (ン)(モノ)エタ/−ルアミンを用い「
臭くない染毛剤」が市販され始めた。然るに最近エタノ
ールアミンの動物の皮膚に対する感作性に関する報文が
発表され、厚生省は表示物質に指定した。人体に対する
影響の真偽は別として問題視されざるを得ない。従って
他のアルカリ物質を探さく中のところ、本発明者はグア
ニジンの塩基性塩が優秀なることを確認し、ここに提案
する次第である。
On the other hand, inorganic alkalis such as KO)T and Na2CO3 tend to remain in the hair. Doing so may cause damage, p
It is limited to craftsmen who use it in small quantities only when raising H. recent years()
! I) Using (n)(mono)ethylamine,
Odorless hair dye has begun to be commercially available. However, recently a report was published regarding the sensitization of ethanolamine to the skin of animals, and the Ministry of Health and Welfare designated it as a labeled substance. Regardless of whether the effect on the human body is true or not, it cannot help but be viewed as a problem. Therefore, while searching for other alkaline substances, the present inventors have confirmed that basic salts of guanidine are excellent and hereby propose them.

そもそも、染毛剤第1剤にアルカリを添加する理由は、
[■第1剤の配合されている薬剤のうち酸性のもの〜中
和を行う目的、■酸素の供給源である第2剤の酸分を中
和する目的(過酸化水素の安定のため酸性となっている
。)、■一般に酸化染料は重合発色する際、アルカリ性
側が反応速度が早いので、第1剤・第2剤混和後もアル
カリ性を保つに必要である目的、■毛髪の細孔に染料を
浸み込ませるため、毛髪を膨潤させるにはアルカリ性が
よいので、そのために添加する目的。]である。
In the first place, the reason why alkali is added to the first part of hair dye is
[■ The purpose of neutralizing the acidic drugs contained in the first agent, ■ The purpose of neutralizing the acid content of the second agent, which is the source of oxygen (acidic to stabilize hydrogen peroxide) ), ■Generally, when oxidation dyes polymerize and develop color, the reaction rate on the alkaline side is faster, so it is necessary to maintain alkalinity even after mixing the first and second agents. The purpose of adding it is that alkalinity is good for swelling the hair in order to absorb the dye. ].

しかし、一般に健康人の頭髪は酸性側に保つのであるか
ら、処理後は毛髪からアルカリをなるべ(除去されねば
ならない。
However, since the hair of healthy people is generally kept on the acidic side, as much alkali as possible must be removed from the hair after treatment.

第1図は各種のアルカリで処理した毛髪のアルカリ残存
率を求めたものである。毛髪を各アルカリのN/10規
定濃度液に浸漬後、水を切り次に精製水に浸漬洗滌する
。(第1回)そのときの pHを測定、以下同様にて数
回求めたものである。この結果アノモニアは最も除去さ
れ易(、次いで炭酸グアニア)であり、トリエタノール
アミ・ン、KOHは悪い結果を得た。アンモニアはドラ
イセント時にも揮散するので最も好ましいが、次いでグ
アニジンである。
Figure 1 shows the alkali residual rates of hair treated with various alkalis. After immersing the hair in a N/10 normal concentration solution of each alkali, the water is drained and the hair is then immersed in purified water for washing. (First time) The pH at that time was measured, and the following measurements were made in the same manner several times. As a result, ammonia was the easiest to remove (followed by guania carbonate), while triethanolamine and KOH gave poor results. Ammonia is the most preferred because it volatilizes during dry cent, followed by guanidine.

塩基性を呈するグアニジン化合物と(−で、水酸化グア
ニジン(溶液としてのみ存在)、炭酸グアニジノ、重炭
酸グアニンン、ホウ酸グアニジン、燐酸ジグアニノン、
有機酸グアニジン等挙げられ本発明ではその回れもが撰
択して使用可能であり例えば水酸化グアニジンのpHは
13.5位でNaOHよりも高く、燐酸ジグアニジンは
8゜5位で、これらの組合せによって極めて広いpH範
囲に調節し得ることが特長である。この事は他の化粧品
分野においても応用面の広いものであるが、それは兎肉
、染毛剤に関しては余りpHが高い場合は毛質に対し悪
影響を与えるのみか染色度もかえって悪い。勿論酸性側
では染色に時間を要する。
Guanidine compounds exhibiting basicity (-, guanidine hydroxide (present only as a solution), guanidine carbonate, guanine bicarbonate, guanidine borate, diguaninone phosphate,
Examples include organic acid guanidine, and in the present invention, any of them can be used selectively. For example, guanidine hydroxide has a pH of 13.5, which is higher than NaOH, and diguanidine phosphate has a pH of 8.5, and a combination of these can be used. The feature is that the pH can be adjusted over an extremely wide range. This has a wide range of applications in other cosmetic fields, but when it comes to rabbit meat and hair dyes, if the pH is too high, it will not only have an adverse effect on the quality of the hair, but will also worsen the degree of dyeing. Of course, dyeing takes time on the acidic side.

アルカリに関し、アルカリの強さく解離度pH)とアル
カリ量とを論じなければならない。アルカリ量の必要量
は前記■〜■に述べた通りであり。
Regarding alkali, the strength of the alkali (dissociation degree (pH)) and the amount of alkali must be discussed. The required amount of alkali is as described in (1) to (2) above.

殊更過剰に加えることはかえって毛質に対し悪影響をも
たらす。本発明者は多年の研究実績により第1剤のpH
は8.5〜10.5 、アルカリ量は前記■を除いて即
ち製品あたり、N/10酸標準液の消費量が5〜30m
1/11の範囲が最適なることを見出にている。
In particular, adding too much will actually have an adverse effect on the hair quality. Based on many years of research results, the inventor has determined that the pH of the first agent
is 8.5 to 10.5, and the amount of alkali is 5 to 30 m2 per product, except for the above (2).
It has been found that a range of 1/11 is optimal.

ここにおいてpHは4倍希釈溶液で行い、N/10酸標
準液の消費量はそれをpHを7.0にする迄の滴定数で
求められる。
Here, the pH was determined using a 4-fold diluted solution, and the consumption amount of the N/10 acid standard solution was determined by the titration number until the pH reached 7.0.

欠配実施例1はグアニジン塩のみのアルカリの場合の具
体例である。
Deficient Example 1 is a specific example in the case of an alkali containing only guanidine salt.

「実施例1.配合薬剤名および配合量 パラフェニレンジアミン     4.00(wt%)
1.5ジヒドロキシナフタレン   1.25パラアミ
ノンフエニルアミン   0.65ニドpフエニレンジ
アミン    0.10プロビレ/グリコール    
  5.0オレイン酸             5.
0ツウイー780        26.0オリーブ油
             2゜エチルアルコール  
     10.0リン酸/グアニジン      1
7,5精製水     28.5 計           100.0 この配合組成物は粘稠淡黄色で7ンモニ7臭が全(なく
、pH8,9、N/10酸標準液消費量は8.0ml/
gであった。
“Example 1. Name of compounded drug and amount paraphenylenediamine 4.00 (wt%)
1.5 dihydroxynaphthalene 1.25 para-aminone phenylamine 0.65 nido p-phenylene diamine 0.10 propylene/glycol
5.0 Oleic acid 5.
0 Twee 780 26.0 Olive oil 2° Ethyl alcohol
10.0 Phosphoric acid/guanidine 1
7.5 Purified water 28.5 Total 100.0 This blended composition is viscous, pale yellow, has no odor, has a pH of 8.9, and has an N/10 acid standard solution consumption of 8.0 ml/
It was g.

本品は過酸化水素を含有する第2剤と混和して毛髪を黒
色に染めるノヤンプー型の染毛用第1剤の例である。」 次に本発明者が提案することは、アンモニアとグアニジ
ンとの併用について検討した。前述のとおり、7ンモニ
7は染毛剤のアルカリとして毛髪に対して優れているが
、臭気の点で使用に難がある。
This product is an example of a Noyanpu-type first agent for hair dyeing that dyes hair black by mixing with a second agent containing hydrogen peroxide. ” Next, the present inventor proposed a study on the combined use of ammonia and guanidine. As mentioned above, 7mmoni7 is excellent for hair as an alkali hair dye, but it is difficult to use due to its odor.

但(−1本発明者はその臭気は程度の問題であるに気付
き、薬剤中のNH3濃度と臭気との関係を不特定の人よ
りアンケートにより求めたyころ、(3゜℃に加温)成
る程度迄は左程嫌悪しない限界のあることが判然とt−
た。この結果を5ランクに纒めて第1表に掲げる。
However, (-1) The present inventor realized that the odor is a matter of degree, and conducted a questionnaire survey of unspecified people to determine the relationship between the NH3 concentration in the drug and the odor (heated to 3°C). It is clear that there is a limit to the extent to which it is not so disgusting.
Ta. The results are summarized into five ranks and listed in Table 1.

第1表 表中の数字は調査対象人員を100 %としての発心= 布である。この結果架剤中N)(3濃度0.8%迄使用
[7ても左程差支えないことを意味している。併しNH
30,8%即ちN/10酸消費量4.7ynl/yでは
、染色剤第1剤として充分といえない。同となれば。
The numbers in Table 1 are based on the number of people surveyed as 100%. As a result, it means that there is no problem even if N) (3 concentration in the cross-agent is used up to 0.8% [7].However, NH
30.8%, ie, N/10 acid consumption of 4.7 ynl/y, cannot be said to be sufficient as a first dye agent. If it's the same.

前記の■の中和のためにも、相当量のアルカリが消費さ
れるからである。
This is because a considerable amount of alkali is consumed also for the neutralization of the above-mentioned item (2).

参考迄に公知の市販品の測定結果を第2表に示す。For reference, measurement results of known commercially available products are shown in Table 2.

第2表 第2表により、第1剤・第2剤の混和後のアルカリ消費
量はS−Aとなる筈であり、混和後は多分に臭気は弱ま
ることになるが、それでも第1剤の開封時、混合時に不
快な印象を与える。もつともシャンプ一式は混和の際の
専門容器が工夫されている。また第2剤の過酸化水素は
酸性側(pI(3,0近辺)において安定であり、第2
表においてとくりクリーム式の場合安定化のため酸の配
合を多くしであることが伺われるが、そうすると第2剤
のフルカリ分量も必然的に多くなる。
Table 2 According to Table 2, the alkali consumption amount after mixing the first and second agents should be S-A, and although the odor will probably be weakened after mixing, the amount of alkali consumed by the first agent will still be Gives an unpleasant impression when opened or mixed. Of course, the shampoo set is designed with a specialized container for mixing. In addition, the second agent, hydrogen peroxide, is stable on the acidic side (pI (near 3.0)), and the second agent is
In the table, it can be seen that in the case of the cream type, a large amount of acid is added for stabilization, but this inevitably increases the amount of potassium in the second agent.

上記の事から総合的にみて、本発明は′第1剤の総アル
カリ分はN/10酸標準液でpH7,0迄滴定するとき
111当り5.0ないし35.0m/とじ、おおむねそ
れが■の目的に対してあてるアルカリはグアニジンとし
、■および■の目的にあてるアルカリは主として7ンモ
ニ7とすることを着想した。このアンモニアは臭気の点
から0.8%以下に抑えるべきであることは前記のとお
りである。グアニジンのアルカリ度はアンモニアより強
いので■に優先的に結合する。但し、このことは飽迄概
念的なものであって、グアニジン塩基が過剰に存在し、
でも、それがpH10、5を超えなげれば染毛に関して
別に悪影響があるわけでない。有無アルカリとしてのN
)(3(%)の測定は試料を100″Cで加熱すればN
H3は揮散するから加熱前後のアルカリをN/10酸標
準液で滴定しその差に0.17を乗ずればよい。
Comprehensively from the above, the present invention shows that the total alkaline content of the first agent is 5.0 to 35.0 m/111 when titrated to pH 7.0 with N/10 acid standard solution; The idea was to use guanidine as the alkali for the purpose of (2), and to use guanidine as the alkali for the purposes of (2) and (2). As mentioned above, this ammonia should be suppressed to 0.8% or less from the viewpoint of odor. Since the alkalinity of guanidine is stronger than that of ammonia, it preferentially binds to ■. However, this is a conceptual concept, and if there is an excess of guanidine base,
However, as long as the pH does not exceed 10.5, there is no particular negative effect on hair dyeing. N as presence or absence of alkali
)(3(%) can be measured by heating the sample at 100"C.
Since H3 evaporates, it is sufficient to titrate the alkali before and after heating with an N/10 acid standard solution and multiply the difference by 0.17.

次にアンモニアとグアニジン塩との併用の場合を実施例
2に掲げる。
Next, Example 2 shows a case where ammonia and guanidine salt are used in combination.

「実施例2 1  パラフェニレンジアミン等の染N     3.
7  (wt%)2  エデト酸ナトリウム     
     0.23 プロピレングリコール    7
54 ポリビニルピロリドン    0.15  ワセ
リン(流動パラフィンを含む)   10.06 セタ
ノール          7.07 ステアリン酸 
       2.08 ラウリル硫酸ナトリウム  
 2゜9  ポリオキシエチレンセチルエーテル   
5.010     ボ リ −<−)80     
                 2.511  ア
ンモニア水(ao%)    −2,012炭酸ジグア
ニジン      8゜13  精製水       
    50.0合     計        io
o、。
“Example 2 1 Dyeing of paraphenylene diamine etc. N 3.
7 (wt%)2 Sodium edetate
0.23 Propylene glycol 7
54 Polyvinylpyrrolidone 0.15 Vaseline (contains liquid paraffin) 10.06 Setanol 7.07 Stearic acid
2.08 Sodium lauryl sulfate
2゜9 Polyoxyethylene cetyl ether
5.010 Bori -<-)80
2.511 Ammonia water (ao%) -2,012 Diguanidine carbonate 8゜13 Purified water
50.0 total io
o.

1〜4.8.11〜13を溶解混合して水ベーストシ、
5〜7.9〜10.を混合和解してオイルベースとし、
両者を70℃に加温しり一混和クリーム状染毛剤第1剤
とする。本品の4倍希釈液のpt−rは10,0、N/
10酸標準液の消費量は241111.#、NH3は0
,57である。」 かくして、髪に対して最も不適性の無機アルカリの添加
を行わなくとも、少量のアルカリでpH&高くすること
が出来た。エタノールアミンに関しては、それ自体の毒
性が確定したわけでないのであって、pHは筒くするこ
とが出来ないもの\1.Hの調節、活性剤との親和等捨
て難い性質を有するので、本発明においてその添加をさ
またげるものでない。
1 to 4. 8. Dissolve and mix 11 to 13 to form a water base,
5-7.9-10. Mix and reconcile to make an oil base,
Both were heated to 70° C. and mixed together to form the first creamy hair dye. The pt-r of the 4-fold dilution of this product is 10.0, N/
The consumption amount of 10 acid standard solution is 241111. #, NH3 is 0
, 57. ” In this way, it was possible to raise the pH level with a small amount of alkali without adding inorganic alkali, which is most unsuitable for hair. Regarding ethanolamine, its own toxicity has not been determined, and the pH cannot be adjusted.\1. Since it has properties that are difficult to discard, such as adjustment of H and affinity with the activator, its addition is not prohibited in the present invention.

【図面の簡単な説明】[Brief explanation of the drawing]

添付図面はアルカリの種類によって毛髪の残存量の比較
をみたもので、横軸に洗滌回数を縦軸にその洗髪液のp
Hを図表にしたものである。 01234   567 洗浄回数
The attached drawing shows a comparison of the amount of hair remaining depending on the type of alkali.The horizontal axis shows the number of washings, and the vertical axis shows the p of the hair wash
This is a diagram of H. 01234 567 Number of washes

Claims (2)

【特許請求の範囲】[Claims] (1)  水酸化グアニ/ン、炭酸グアニジン、重炭酸
グアニジン、燐酸グアニジン、ホウ酸グ7ニンン、有機
酸グアニ/ンの一種また二種以上をア/Lカリ分として
配合し、pH8,5〜10,5 、 N/、1θ酸標準
液の消費量が5〜35 Ml/77であることを特徴と
する染毛のだめの第1剤。
(1) One or more types of guanidine hydroxide, guanidine carbonate, guanidine bicarbonate, guanidine phosphate, guanidine boric acid, and organic acid guanidine are blended as the a/L potash content, and the pH is 8.5- A first agent for a hair dye pot, characterized in that the consumption amount of a 10,5, N/, 1θ acid standard solution is 5 to 35 Ml/77.
(2)  前記N/10酸標準液の消費量が5〜35T
nll&であって、そのアルカリ分のうち、■、として
0.8%(重t)以下の7ンモニ7を含有することを特
徴とする特許請求の範囲第1項記載の染毛のための第1
剤っ
(2) The consumption amount of the N/10 acid standard solution is 5 to 35T.
nll&, which contains 0.8% (weight t) or less of 7 mmoni 7 as ■ out of its alkaline content, as set forth in claim 1. 1
Agent
JP13270781A 1981-08-26 1981-08-26 First solution for hair dyeing Granted JPS5835106A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13270781A JPS5835106A (en) 1981-08-26 1981-08-26 First solution for hair dyeing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13270781A JPS5835106A (en) 1981-08-26 1981-08-26 First solution for hair dyeing

Publications (2)

Publication Number Publication Date
JPS5835106A true JPS5835106A (en) 1983-03-01
JPH0231690B2 JPH0231690B2 (en) 1990-07-16

Family

ID=15087676

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13270781A Granted JPS5835106A (en) 1981-08-26 1981-08-26 First solution for hair dyeing

Country Status (1)

Country Link
JP (1) JPS5835106A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH1025230A (en) * 1996-07-12 1998-01-27 Kao Corp First agent composition for dyeing hair
US6071504A (en) * 1997-07-09 2000-06-06 Kao Corporation Hair treatment composition comprising alkalizing agent
ITMI20081764A1 (en) * 2008-10-03 2010-04-04 Eurosirel Spa COMPOSITION SUITABLE FOR CUTANEOUS APPLICATION WITH A GELIFIED STRUCTURE USED AS A VEHICLE FOR THE SALE OF ACTIVE PRINCIPLES.
FR2940056A1 (en) * 2008-12-19 2010-06-25 Oreal Coloring keratin fibers, preferably human keratin fibers such as hair, comprises applying on the fibers a composition comprising e.g. surfactants, cosmetic composition comprising e.g. direct dyes and composition comprising oxidizing agent
JP2012126661A (en) * 2010-12-14 2012-07-05 Paimore Co Ltd Second component composition of two-component dyeing agent
JP2013512861A (en) * 2009-10-16 2013-04-18 ロレアル Composition comprising at least one 1,8-dihydroxynaphthalene derivative and at least one basifying agent different from aqueous ammonia, and method for dyeing keratin fibers using this composition
US11691035B2 (en) 2008-12-19 2023-07-04 L'oreal Oxidizing composition for the treatment of keratin fibers comprising at least one cationic polymer, at least one fatty amide and at least one anti-oxygen agent

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JPH0686915U (en) * 1993-05-31 1994-12-20 村田機械株式会社 Gate cut device chuck structure

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Publication number Priority date Publication date Assignee Title
EP0026473A1 (en) * 1979-09-28 1981-04-08 Wella Aktiengesellschaft Oxidative hair-dyeing composition

Patent Citations (1)

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Publication number Priority date Publication date Assignee Title
EP0026473A1 (en) * 1979-09-28 1981-04-08 Wella Aktiengesellschaft Oxidative hair-dyeing composition

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH1025230A (en) * 1996-07-12 1998-01-27 Kao Corp First agent composition for dyeing hair
US6071504A (en) * 1997-07-09 2000-06-06 Kao Corporation Hair treatment composition comprising alkalizing agent
ITMI20081764A1 (en) * 2008-10-03 2010-04-04 Eurosirel Spa COMPOSITION SUITABLE FOR CUTANEOUS APPLICATION WITH A GELIFIED STRUCTURE USED AS A VEHICLE FOR THE SALE OF ACTIVE PRINCIPLES.
FR2940056A1 (en) * 2008-12-19 2010-06-25 Oreal Coloring keratin fibers, preferably human keratin fibers such as hair, comprises applying on the fibers a composition comprising e.g. surfactants, cosmetic composition comprising e.g. direct dyes and composition comprising oxidizing agent
US11691035B2 (en) 2008-12-19 2023-07-04 L'oreal Oxidizing composition for the treatment of keratin fibers comprising at least one cationic polymer, at least one fatty amide and at least one anti-oxygen agent
JP2013512861A (en) * 2009-10-16 2013-04-18 ロレアル Composition comprising at least one 1,8-dihydroxynaphthalene derivative and at least one basifying agent different from aqueous ammonia, and method for dyeing keratin fibers using this composition
JP2012126661A (en) * 2010-12-14 2012-07-05 Paimore Co Ltd Second component composition of two-component dyeing agent

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