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JPH09278636A - Dyeing agent for hair - Google Patents

Dyeing agent for hair

Info

Publication number
JPH09278636A
JPH09278636A JP11558596A JP11558596A JPH09278636A JP H09278636 A JPH09278636 A JP H09278636A JP 11558596 A JP11558596 A JP 11558596A JP 11558596 A JP11558596 A JP 11558596A JP H09278636 A JPH09278636 A JP H09278636A
Authority
JP
Japan
Prior art keywords
dye
hair
dyeing
dyes
acid
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
JP11558596A
Other languages
Japanese (ja)
Inventor
Mutsumi Noguchi
睦 野口
Megumi Yoshimoto
恵 吉本
Yuichi Nishida
勇一 西田
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.)
Lion Corp
Original Assignee
Lion Corp
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 Lion Corp filed Critical Lion Corp
Priority to JP11558596A priority Critical patent/JPH09278636A/en
Publication of JPH09278636A publication Critical patent/JPH09278636A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a dyeing agent for hair, at least harmless to human bodies, and having good dyeing effect and durability. SOLUTION: This dyeing agent for hair is obtained by adding and dissolving urea, benzyl alcohol and ethanol in an aqueous dye solution containing at least one dye of an acidic dye, a basic dye, a reactive dye and a disperse dye.

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】本発明は毛髪用染色剤に関
し、詳しくは、酸性染料、塩基性染料、反応性染料及び
分散染料から選ばれる人体に無害な染料の少なくとも1
種を含有し、人毛、羊毛などのケラチン系繊維を低温度
で任意の色調、濃度に長期間染色できる、安全で染着性
の良好なケラチン系繊維用染色剤に係るものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a hair dye, and more specifically, at least one of dyes harmless to the human body selected from acid dyes, basic dyes, reactive dyes and disperse dyes.
The present invention relates to a safe and good dyeing agent for keratin-based fibers, which contains seeds and is capable of dyeing keratin-based fibers such as human hair and wool at low temperature for a desired color tone and concentration for a long time.

【0002】[0002]

【従来の技術】従来最も普通に使用されている染毛剤は
フェニレンジアミン系の酸化染料を主成分としてなる
が、この酸化染料はアレルギー性症をおこす可能性があ
るばかりでなく、染毛にとっては皮膚刺激や毛髪損傷な
どを生じるアルカリおよび過酸化水素水を不可欠とする
ので、安全性の面からも使用上の便利さの上からも好ま
しいものとはいえない。このため、フェニレンジアミン
系の酸化染料を使用しない他の染毛剤が要望されてお
り、近年になって比較的安全性の高い反応性染料、分散
染料などを使用する染毛剤が提案されるようになってき
ている。しかし、これら提案されている反応性染料、分
散染料を使用した染毛剤は室温ではケラチン系繊維に対
する染着性が悪く、チオグリコール酸塩などのメルカプ
タン系の還元剤などで繊維を前処理しなければならない
難点があり、人体に対して使用可能な温度範囲ならびに
pH範囲で満足できる染色濃度に染毛できる染毛剤を得
ることは不可能であった。
2. Description of the Related Art The most commonly used hair dyes in the past are mainly composed of phenylenediamine-based oxidative dyes. These oxidative dyes not only cause allergic diseases but also cause hair dyeing. Since it requires an alkali and a hydrogen peroxide solution that cause skin irritation and hair damage, it is not preferable in terms of safety and convenience in use. Therefore, there is a demand for other hair dyes that do not use phenylenediamine-based oxidative dyes, and in recent years hair dyes that use relatively safe reactive dyes, disperse dyes, etc. have been proposed. Is starting to appear. However, these proposed hair dyes using reactive dyes and disperse dyes have poor dyeing properties to keratin fibers at room temperature, and fibers are pretreated with a mercaptan reducing agent such as thioglycolate. However, it has been difficult to obtain a hair dye capable of dyeing hair to a satisfactory dyeing concentration in a temperature range and a pH range that can be used for the human body.

【0003】他方、羊毛を100℃以下の温度で染色す
る低温染色法として、染浴にベンジルアルコールなどの
溶剤を添加したり、尿素のような膨潤剤を添加して使用
することが知られている。ここで、ベンジルアルコール
の水への溶解度はせいぜい3.0%(W/V)に過ぎ
ず、従って添加量は通常0.1〜3.0容量%で、尿素
の場合は5〜40重量%(W/V)であり、加えて、何
れの場合も浴温は70℃以上を必要とし、常温ないし体
温付近の温度での人毛を含めた染色では十分な染色効果
は得られず、また耐洗濯性、耐摩擦性も低く、洗剤を用
いた洗濯で容易に脱色する欠点があった。
On the other hand, as a low temperature dyeing method for dyeing wool at a temperature of 100 ° C. or lower, it is known to add a solvent such as benzyl alcohol or a swelling agent such as urea to a dyeing bath. There is. Here, the solubility of benzyl alcohol in water is at most 3.0% (W / V), so the addition amount is usually 0.1 to 3.0% by volume, and in the case of urea 5 to 40% by weight. (W / V), in addition, in any case, the bath temperature must be 70 ° C. or higher, and a sufficient dyeing effect cannot be obtained by dyeing human hair at a temperature near room temperature or body temperature. It also has low washing resistance and abrasion resistance, and has the drawback that it can be easily decolorized by washing with a detergent.

【0004】[0004]

【発明が解決しようとする課題】こうした欠点を解消す
るものとして、酸性染料、塩基性染料、反応性染料およ
び分散染料よりなる群から選ばれた染料の1種あるいは
それ以上を含有した水性染浴に、尿素とベンジルアルコ
ールとを添加溶解させたことを特徴とするケラチン系繊
維用染色剤が開発された(特開昭52−91028
号)。この染色剤の使用によれば、人毛、羊毛などのケ
ラチン系繊維を低温度で良好に染色することができる。
しかしながら、この染色剤は特にその染料の染着力及び
耐久性の点で本発明者らが意図している程度には達して
いない。このため、本発明の目的は顕著な染色効果が達
成され、その耐久性が極めて良好となる毛髪用染色剤を
提供することである。
As a solution to these problems, an aqueous dye bath containing one or more dyes selected from the group consisting of acid dyes, basic dyes, reactive dyes and disperse dyes. In addition, a dyeing agent for keratin-based fibers, which is characterized in that urea and benzyl alcohol are added and dissolved, has been developed (JP-A-52-91028).
issue). By using this dyeing agent, keratin fibers such as human hair and wool can be dyed well at low temperature.
However, this dyeing agent has not reached the level intended by the present inventors, particularly in terms of dyeing power and durability of the dye. Therefore, an object of the present invention is to provide a hair dyeing agent which achieves a remarkable dyeing effect and has extremely good durability.

【0005】[0005]

【課題を解決するための手段】本発明者らは、特開昭5
2−91028号に記載された染色剤にさらにエタノー
ルを添加溶解させることによって、前記の目的が充分達
成できることを見出し、本発明をなしえたものである。
従って、本発明によれば、酸性染料、塩基性染料、反応
性染料及び分散染料よりなる群から選ばれた染料の少な
くとも1種を含有した水性染浴に、尿素、ベンジルアル
コール及びエタノールを添加溶解させたことを特徴とす
る毛髪用染色剤が提供される。
Means for Solving the Problems The inventors of the present invention have disclosed in Japanese Patent Laid-Open No.
The present invention has been completed by discovering that the above object can be sufficiently achieved by further adding and dissolving ethanol to the dyeing agent described in JP-A 2-91028.
Therefore, according to the present invention, urea, benzyl alcohol and ethanol are added and dissolved in an aqueous dye bath containing at least one dye selected from the group consisting of acid dyes, basic dyes, reactive dyes and disperse dyes. A hair dye is provided.

【0006】[0006]

【発明の実施の形態】以下、本発明をさらに詳細に説明
する。本発明の毛髪用染色剤においては、尿素が0.
1〜10重量%、ベンジルアルコールが10〜20重量
%、エタノールが10〜30重量%の範囲内で添加溶解
されているのが望ましく、浸透剤、分散剤、香料、粘
度調整剤、pH調整剤、紫外線吸収剤などの添加剤をさ
らに適宜添加しておくのが望ましく、また特に人体に
安全な染料を選択して含有せしめ、pHが染料に応じて
2〜10の範囲内に調整されているのが望ましい。
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in more detail. In the hair dye of the present invention, urea is 0.
1 to 10% by weight, benzyl alcohol is 10 to 20% by weight, and ethanol is preferably added and dissolved within the range of 10 to 30% by weight, and a penetrant, a dispersant, a fragrance, a viscosity adjusting agent, a pH adjusting agent. , It is desirable to further add additives such as UV absorbers, and a dye that is particularly safe for the human body is selected and contained, and the pH is adjusted within the range of 2 to 10 according to the dye. Is desirable.

【0007】本発明で使用する染料は人体に対して有害
な作用を有しない酸性染料、塩基性染料、反応性染料、
分散染料から任意に選ぶことができ、これには医療、医
薬部外品および化粧品の着色に使用することが許されて
いる「医薬品等に使用することができるタール色素を定
める省令」に掲示されている法定色素、あるいはアント
ラキノン系化合物やイリドイド化合物及びセコイリド化
合物なども包含され、これらには例えば下記の染料が使
用できる。
The dyes used in the present invention are acid dyes, basic dyes, reactive dyes, which have no harmful effect on the human body.
It can be arbitrarily selected from disperse dyes, and it is posted in the "Ministerial Ordinance for Defining Tar Dyes that can be Used for Pharmaceuticals", which is allowed to be used for coloring medical products, quasi drugs, and cosmetics. The legal dyes mentioned above, or anthraquinone compounds, iridoid compounds, secoilide compounds, and the like are also included. For example, the following dyes can be used.

【0008】赤色104号(法定色素名、以下同じ)、
赤色105号、赤色106号(以上、酸性染料)、赤色
201号(酸性染料)、赤色206号(顔料)、赤色2
13号(塩基性染料)、赤色227号、赤色401号、
赤色503号、赤色504号(以上、酸性染料)、橙色
402号、橙色205号(以上、酸性染料)、黄色4
号、黄色5号、黄色203号、黄色402号、黄色40
3号(以上、酸性染料)、黄色405号(油溶染料)、
緑色3号、緑色205号、緑色402号(以上、酸性染
料)、青色1号、青色2号、青色203号、青色205
号(以上、酸性染料)、紫色401号(酸性染料)、褐
色201号(酸性染料)、黒色401号(酸性染料)な
ど。
Red No. 104 (legal dye name, the same applies hereinafter),
Red No. 105, Red No. 106 (or more acid dye), Red No. 201 (acid dye), Red No. 206 (pigment), Red 2
No. 13 (basic dye), Red No. 227, Red No. 401,
Red No. 503, Red No. 504 (or more acid dye), Orange No. 402, orange No. 205 (or more acid dye), Yellow 4
No., Yellow No. 5, Yellow No. 203, Yellow No. 402, Yellow 40
No. 3 (above, acid dye), yellow No. 405 (oil soluble dye),
Green No. 3, Green No. 205, Green No. 402 (above, acid dye), Blue No. 1, Blue No. 2, Blue No. 203, Blue No. 205
No. (above, acid dye), purple No. 401 (acid dye), brown No. 201 (acid dye), black No. 401 (acid dye), etc.

【0009】本発明の毛髪用染色剤は、既述のとおり、
酸化染料、塩基性染料、反応性染料及び分散染料よりな
る群から選ばれた染料の1種又は2種以上を含む水性染
浴に、尿素とベンジルアルコールとエタノールとをとも
に添加することを特徴とし、これによって前記の顕著な
効果をあげている。このような効果が得られる理由はお
そらく尿素とエタノールとの共存によってベンジルアル
コールの溶解度を著しく上昇させ、それが染料の染着力
を増大したものと考えられる。また、本発明品において
は、尿素の毛髪軟化作用により、処理後の毛髪になめら
かさや指通りの良さなど豊かな風合いを与える効果がも
たらされるが、こうしたことの理由はいまだ解明されて
いない。
The hair dye of the present invention is as described above.
Characteristically, urea, benzyl alcohol, and ethanol are added together to an aqueous dye bath containing one or more dyes selected from the group consisting of oxidation dyes, basic dyes, reactive dyes, and disperse dyes. By this, the above-mentioned remarkable effect is exhibited. The reason why such an effect is obtained is probably that the coexistence of urea and ethanol markedly increased the solubility of benzyl alcohol, which increased the dyeing power of the dye. Further, in the product of the present invention, the hair softening action of urea brings about an effect of giving the treated hair a rich texture such as smoothness and good finger feeling, but the reason for this has not been clarified yet.

【0010】本発明者らは酸化染料、塩基性染料、反応
性染料及び分散染料を単独で含む染浴及び2種以上の染
料を含む染浴についても染色実験を行い尿素およびベン
ジルアルコール、エタノールを特に上記の範囲内で共に
添加するときは人体に耐え得る低温(約50℃以下)
で、また人体に悪影響のないpH範囲(約pH2〜1
1)で毛髪および他のケラチン系繊維を極めて容易にか
つ希望の色調、濃度に半永久的に染色できしかもこの染
浴は悪臭もなく、人体に対しても何等有害な作用のない
ことを確認した。
The present inventors have conducted dyeing experiments on dyeing baths containing an oxidative dye, a basic dye, a reactive dye and a disperse dye alone and a dyeing bath containing two or more kinds of dyes, and added urea, benzyl alcohol and ethanol. Especially when added together within the above range, a low temperature that can withstand the human body (about 50 ° C or less)
In addition, a pH range that does not adversely affect the human body (about pH 2-1
It was confirmed in 1) that hair and other keratin fibers can be dyed extremely easily and semi-permanently to a desired color tone and density, and that this dye bath has no foul odor and has no harmful effect on the human body. .

【0011】更に、本発明の染毛剤によって染色した山
羊毛、羊毛のようなケラチン系繊維および毛髪に対し洗
剤を含む温水洗濯試験、耐光試験および摩擦試験を行っ
てその染色堅牢度を調べたが、ほとんど脱色、変色は見
られず、ほぼ永久的な染毛および染色が達成できること
も確かめられた。
Further, goat hair, keratinous fibers such as wool dyed with the hair dye of the present invention, and hair were subjected to a hot water washing test containing a detergent, a light resistance test and a rubbing test to examine the dye fastness. However, almost no decolorization or discoloration was observed, and it was also confirmed that almost permanent hair dyeing and dyeing can be achieved.

【0012】本発明の染色剤は人毛およびケラチン系繊
維の染色に有効であることは上述の通りであるが、本発
明の染色剤においては染料の種類に応じて染浴を希望の
pH値に調整するのが望ましい。そこでのpH調整剤と
しては、有機酸として例えばクエン酸、グリコール酸、
コハク酸、酒石酸、乳酸、フマル酸、リンゴ酸、レブリ
ン酸、酪酸、吉草酸、シュウ酸、マレイン酸、フマル
酸、マンデル酸等を挙げることができ、無機酸として例
えばリン酸、硫酸、硝酸等を挙げることができる。塩基
として水酸化ナトリウム、水酸化カリウム、水酸化カル
シウム、モノエタノールアミン、ジメタノールアミン、
トリエタノールアミン、アミノジヒドロキシメチルプロ
パンジオール、2−アミノ−2−メチル−1−プロパノ
ール、2−アミノ−2−メチル−1,3−プロパンジオ
ール等を挙げることができる。また、この他にもアルギ
ニンなど塩基性アミノ酸を用いることもでき、更には、
これらの酸及び塩基を共存させ、例えばナトリウム塩、
カリウム塩、アンモニウム塩、トリエタノールアミン塩
などのアルカノールアミン塩等を用いることができる。
As described above, the dyeing agent of the present invention is effective for dyeing human hair and keratin fibers. However, in the dyeing agent of the present invention, the dyeing bath is set to a desired pH value depending on the type of the dyeing agent. It is desirable to adjust to. Examples of the pH adjuster there include organic acids such as citric acid, glycolic acid,
Examples thereof include succinic acid, tartaric acid, lactic acid, fumaric acid, malic acid, levulinic acid, butyric acid, valeric acid, oxalic acid, maleic acid, fumaric acid, and mandelic acid. Examples of inorganic acids include phosphoric acid, sulfuric acid, nitric acid, etc. Can be mentioned. Sodium hydroxide, potassium hydroxide, calcium hydroxide, monoethanolamine, dimethanolamine as a base,
Examples thereof include triethanolamine, aminodihydroxymethylpropanediol, 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-1,3-propanediol and the like. In addition to this, a basic amino acid such as arginine can also be used, and further,
Coexistence of these acids and bases, for example sodium salt,
Alkanolamine salts such as potassium salt, ammonium salt and triethanolamine salt can be used.

【0013】更に、浸透、分散を増進させるための浸透
剤、分散剤、特に染毛剤として使用する場合に染浴の毛
髪への付着をよくするためヒドロキシエチルセルロース
などの増粘剤や、シリコーン類などの感触向上剤、およ
び香料、防腐剤、紫外線吸収剤、酸化防止剤、殺菌剤な
ど従来化粧品で通常使用されている添加剤を適宜添加で
きることは勿論である。
Further, a penetrant for enhancing penetration and dispersion, a dispersant, particularly a thickener such as hydroxyethyl cellulose and silicones for improving adhesion to the hair of the dye bath when used as a hair dye. It is needless to say that it is possible to appropriately add a texture improver such as the above, and additives normally used in conventional cosmetics such as a fragrance, an antiseptic, an ultraviolet absorber, an antioxidant and a bactericide.

【0014】[0014]

【実施例】次に、実施例を挙げ本発明を説明する。な
お、処方中の各成分の濃度は重量基準で表わし、全体で
100部又は100%になるようにした。本発明品、比
較品の評価は下記の基準に従った。 (1)染色時(シャンプー1回)の染毛性 白髪毛束約1gに対し、本発明品、比較品を1g塗布
し、15分放置した。その後、流水ですすぎ、シャンプ
ー/リンスをし、乾燥した。染色毛束を色差計(日本電
色社製)で、L、a、b値を測定し、未染色毛との色差
(ΔE)を求め、染毛性を評価した。なお、ΔE1はそ
の数値が大きい程染毛性がよいことを意味する (2)染毛時(シャンプー1回)の毛髪の感触 白髪毛束約1gに対し、本発明品、比較品を1g塗布
し、上記と同様に処理して仕上がりを専門パネラー5名
で評価した。 ◎:非常になめらかであり、指通りが良い ○:なめらかであり指通りが良い △:髪がすべらず、ややざらつく ×:きしみがあり、かなりざらつく
EXAMPLES Next, the present invention will be described with reference to examples. The concentration of each component in the formulation was expressed on a weight basis, and was set to 100 parts or 100% as a whole. The evaluation of the product of the present invention and the comparative product was based on the following criteria. (1) Hair dyeability during dyeing (once with shampoo) About 1 g of a white hair bundle was coated with 1 g of the product of the present invention and the comparative product and left for 15 minutes. Then rinsed under running water, shampoo / rinse and dried. The dyed hair bundle was measured for L, a, and b values with a color difference meter (manufactured by Nippon Denshoku Co., Ltd.), the color difference (ΔE) from the undyed hair was determined, and the hair dyeability was evaluated. In addition, ΔE 1 means that the larger the value is, the better the hair dyeing property is. (2) Feeling of hair at the time of dyeing hair (1 time of shampoo) About 1 g of a white hair bundle, 1 g of the present invention product and the comparative product It was applied and treated in the same manner as described above, and the finish was evaluated by 5 professional panelists. ◎: Very smooth with good finger contact ○: Smooth and with good finger contact △: Hair does not slip and is slightly rough ×: Has squeaky texture and is considerably rough

【0015】実施例1〜4、比較例1〜5 下記表1に示す組成からなる本発明の染毛剤組成物(実
施例1〜4)及び比較の染毛剤組成物(比較例1〜5)
をそれぞれ調製し、それぞれの染毛剤組成物の染毛性及
び染色後の毛髪の感触を評価し、これらを表1に示し
た。
Examples 1 to 4, Comparative Examples 1 to 5 Hair dye compositions of the present invention (Examples 1 to 4) and comparative hair dye compositions (Comparative Examples 1 to 1) having the compositions shown in Table 1 below. 5)
Was prepared, and the dyeability of each hair dye composition and the feel of the hair after dyeing were evaluated, and these are shown in Table 1.

【0016】[0016]

【表1】 [Table 1]

【0017】 実施例5(黒色染毛剤の調製) ナフトールブルーブラック(酸性染料) 0.5% オレンジII(酸性染料) 0.2% クエン酸 0.5% ベンジルアルコール 15.0% 尿素 7.0% エタノール 20.0% ポリオキシエチレンノニルフェニルエーテル 0.1% (浸透剤用界面活性剤) 精製水 残 部 まず水に尿素を溶し、これにベンジルアルコールを添加
して溶解させる。この溶液にナフトールブルーブラック
およびオレンジIIを溶し、さらにポリオキシエチレンノ
ニルフェニルエーテルを加え、最後にクエン酸でpH
3.0〜3.5に調整した。この染浴を染毛に使用する
場合には、毛髪を洗浄し、これに上記の染毛剤を常法に
従って塗布し、室温あるいは50℃以下の弱い加温の下
で10〜30分放置し、最後に洗髪、乾燥する。その結
果、永久的な黒色染毛が達成された。また、この染浴は
羊毛、山羊毛のようなケラチン系繊維の染色にも同様の
手段で使用でき、良好な結果が得られた。
Example 5 (Preparation of black hair dye) Naphthol blue black (acid dye) 0.5% Orange II (acid dye) 0.2% Citric acid 0.5% Benzyl alcohol 15.0% Urea 7. 0% ethanol 20.0% polyoxyethylene nonylphenyl ether 0.1% (surfactant for penetrant) Purified water balance First, urea is dissolved in water, and benzyl alcohol is added to this to dissolve it. Dissolve naphthol blue black and orange II in this solution, add polyoxyethylene nonyl phenyl ether, and finally add citric acid to adjust the pH.
Adjusted to 3.0-3.5. When this dye bath is used for dyeing hair, the hair is washed, the above hair dye is applied thereto according to a conventional method, and the hair is left to stand at room temperature or under mild heating at 50 ° C. or lower for 10 to 30 minutes. Finally, wash and dry your hair. As a result, a permanent black hair dyeing was achieved. This dye bath can also be used for dyeing keratin-based fibers such as wool and goat hair by the same means, and good results were obtained.

【0018】 実施例6(赤色染毛剤の調製) ローダミンB(塩基性染料) 0.5% アンモニア水(28%) 0.1% ベンジルアルコール 4.0% 尿素 10.0% エタノール 25.0% ヒドロキシエチルセルローズ(増粘剤) 2.0% 香料 0.05% 精製水 残 部 精製水に尿素、次いでベンジルアルコールを溶し、この
溶液にヒドロキシエチルセルローズを溶して粘稠な液状
とし、これにローダミンBおよび香料を溶し、最後にア
ンモニア水でpH9.5〜10.0に調整した。この染
浴(赤色染毛剤)は特に染毛剤として好適であって実施
例1と同様な方法で適用する時永久的な赤色染毛が達成
された。
Example 6 (Preparation of red hair dye) Rhodamine B (basic dye) 0.5% Aqueous ammonia (28%) 0.1% Benzyl alcohol 4.0% Urea 10.0% Ethanol 25.0 % Hydroxyethyl cellulose (thickener) 2.0% Perfume 0.05% Purified water balance Urea and then benzyl alcohol are dissolved in purified water, and hydroxyethyl cellulose is dissolved in this solution to give a viscous liquid, Rhodamine B and a fragrance | flavor were melt | dissolved in this, and pH was adjusted to 9.5-10.0 with ammonia water finally. This dyebath (red hair dye) is particularly suitable as a hair dye, and when applied in the same manner as in Example 1, a permanent red hair dye was achieved.

【0019】 実施例7(橙色染毛剤の調製) プロシオンブリリアントレッド2BS* 0.2% プロシオンイエローRS* 0.2% 乳酸 0.5% ベンジルアルコール 15.0% 尿素 5.0% エタノール 30.0% ラウリルベタイン(界面活性剤) 0.2% ヒドロキシエチルセルローズ 1.8% 精製水 残 部 (*はICI社製造の反応性染料) 精製水に尿素、ついでベンジルアルコールを溶し、この
溶液にヒドロキシエチルセルローズを溶して粘稠な液状
とし、さらにラウリルベタインおよびプロシオンブリリ
アントレッド2BSならびにプロシオンイエローRSを
溶し、最後に乳酸でpHを3.0〜3.5に調整した。
この染浴は実施例1と同様染毛用として特に好適に使用
できた。
Example 7 (Preparation of orange hair dye) Procion Brilliant Red 2BS * 0.2% Procion Yellow RS * 0.2% Lactic acid 0.5% Benzyl alcohol 15.0% Urea 5.0% Ethanol 30. 0% Lauryl betaine (surfactant) 0.2% Hydroxyethyl cellulose 1.8% Purified water Remainder (* Reactive dye manufactured by ICI) Urea and then benzyl alcohol are dissolved in purified water and added to this solution. Hydroxyethyl cellulose was dissolved into a viscous liquid, and lauryl betaine, Procion Brilliant Red 2BS and Procion Yellow RS were dissolved, and finally the pH was adjusted to 3.0 to 3.5 with lactic acid.
As in Example 1, this dyebath could be used particularly suitably for hair dyeing.

【0020】 実施例8(褐色染毛剤の調製) ミケトンファーストブラウンML** 0.5% ミケトンファーストブラックBGL** 0.2% ベンジルアルコール 14.0% 尿素 5.0% エタノール 15.0% ポリオキシエエチレンアルカノールアミド 0.1% (界面活性剤) ナフタレンスルホン酸縮合物(分散剤) 0.1% 香料 0.05% (**は三井化学社製の分散染料) 精製水に尿素、ついでベンジルアルコールを溶し、この
溶液にポリオキシエエチレンアルカノールアミドを溶
し、これに予めナフタレンスルホン酸縮合物に分散させ
たミケトンファーストブラウンMLおよびミケトンファ
ーストブラックBGLを加え、最後に香料を添加した。
この染浴は染毛にもまた羊毛などのケラチン系繊維の染
色にもとに良好に使用できた。
Example 8 (Preparation of brown hair dye) Miketone Fast Brown ML ** 0.5% Miketone Fast Black BGL ** 0.2% Benzyl Alcohol 14.0% Urea 5.0% Ethanol 15. 0% Polyoxyethylene alkanolamide 0.1% (surfactant) Naphthalene sulfonic acid condensate (dispersant) 0.1% Perfume 0.05% (** is a disperse dye manufactured by Mitsui Chemicals, Inc.) Purified water Urea and then benzyl alcohol are dissolved, polyoxyethylene alkanolamide is dissolved in this solution, and Miketone Fast Brown ML and Miketone Fast Black BGL, which are previously dispersed in a naphthalenesulfonic acid condensate, are added thereto, and finally, Perfume was added.
This dyebath was originally suitable for dyeing hair and dyeing keratin fibers such as wool.

【0021】 実施例19(赤褐色毛色剤の調製) ベイシックブラックBN(塩基性染料) 0.1% ローダミンB(塩基性染料) 0.2% タートラジン(酸性染料) 0.1% アリズロールパープル(酸性染料) 0.1% ベンジルアルコール 12.0% 尿素 3.0% エタノール 20.0% クエン酸 1.0% クエン酸ナトリウム 1.0% ヒドロキシエチルセルローズ 2.0% 精製水 残 部 精製水に尿素を溶し、さらにベンジルアルコールを溶
し、この溶液にヒドロキシエチルセルローズを溶して粘
稠な液状とし、これにベイシックブラックBN、ローダ
ミンB、タートラジン、アリズロールパープルを加え、
最後にクエン酸とクエン酸ナトリウムとでpH6.0〜
7.0に調整した。この染浴は実施例1と同様染毛剤と
して好適に使用され、優れた結果が得られた。
Example 19 (Preparation of Reddish Brown Hair Coloring Agent) Basic Black BN (Basic Dye) 0.1% Rhodamine B (Basic Dye) 0.2% Tartrazine (Acidic Dye) 0.1% Alizulol Purple (Acidic) Dye) 0.1% Benzyl alcohol 12.0% Urea 3.0% Ethanol 20.0% Citric acid 1.0% Sodium citrate 1.0% Hydroxyethyl cellulose 2.0% Purified water Remainder Urea in purified water , Benzyl alcohol, hydroxyethyl cellulose is dissolved in this solution to make a viscous liquid, to which basic black BN, rhodamine B, tartrazine, and alizrole purple are added,
Finally, the pH is 6.0 with citric acid and sodium citrate.
It was adjusted to 7.0. This dyebath was suitably used as a hair dye as in Example 1, and excellent results were obtained.

【0022】[0022]

【発明の効果】本発明の毛髪用染色剤の使用によれば、
染料の染着力が著しく向上するとともに耐久性も極めて
良好なものになる。
According to the use of the hair dye of the present invention,
Dyeing power of the dye is remarkably improved, and durability is also very good.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 酸性染料、塩基性染料、反応性染料及び
分散染料よりなる群から選ばれた染料の少なくとも1種
を含有した水性染浴に、尿素、ベンジルアルコール及び
エタノールを添加溶解させたことを特徴とする毛髪用染
色剤。
1. Urea, benzyl alcohol and ethanol are added and dissolved in an aqueous dye bath containing at least one dye selected from the group consisting of acid dyes, basic dyes, reactive dyes and disperse dyes. A dyeing agent for hair characterized by:
JP11558596A 1996-04-12 1996-04-12 Dyeing agent for hair Pending JPH09278636A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11558596A JPH09278636A (en) 1996-04-12 1996-04-12 Dyeing agent for hair

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11558596A JPH09278636A (en) 1996-04-12 1996-04-12 Dyeing agent for hair

Publications (1)

Publication Number Publication Date
JPH09278636A true JPH09278636A (en) 1997-10-28

Family

ID=14666242

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11558596A Pending JPH09278636A (en) 1996-04-12 1996-04-12 Dyeing agent for hair

Country Status (1)

Country Link
JP (1) JPH09278636A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000344639A (en) * 1999-03-26 2000-12-12 Kanebo Ltd Acid hair dye for wet hair and method of hair dyeing
JP2003246715A (en) * 2002-02-22 2003-09-02 Nikko Chemical Co Ltd Hair dye composition
US8343238B1 (en) 2011-12-30 2013-01-01 L'oreal Sa. Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases
US8506651B2 (en) 2011-12-30 2013-08-13 L'oreal S.A. Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases
US8556994B2 (en) 2011-12-30 2013-10-15 L'oreal Process for altering the appearance of hair using a composition containing direct dyes and non-hydroxide bases
US8591872B2 (en) 2011-12-30 2013-11-26 L'oreal Composition and process for reducing the curl and frizziness of hair
US10596100B2 (en) 2012-12-19 2020-03-24 L'oreal Cosmetic compositions containing an alkoxysilane and a silsesquioxane resin

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000344639A (en) * 1999-03-26 2000-12-12 Kanebo Ltd Acid hair dye for wet hair and method of hair dyeing
JP2003246715A (en) * 2002-02-22 2003-09-02 Nikko Chemical Co Ltd Hair dye composition
US8343238B1 (en) 2011-12-30 2013-01-01 L'oreal Sa. Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases
US8506651B2 (en) 2011-12-30 2013-08-13 L'oreal S.A. Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases
US8556994B2 (en) 2011-12-30 2013-10-15 L'oreal Process for altering the appearance of hair using a composition containing direct dyes and non-hydroxide bases
US8591872B2 (en) 2011-12-30 2013-11-26 L'oreal Composition and process for reducing the curl and frizziness of hair
US10596100B2 (en) 2012-12-19 2020-03-24 L'oreal Cosmetic compositions containing an alkoxysilane and a silsesquioxane resin
US11324689B2 (en) 2012-12-19 2022-05-10 L'oreal Cosmetic compositions containing an alkoxysilane and a silsesquioxane resin

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