JPH0410443B2 - - Google Patents
Info
- Publication number
- JPH0410443B2 JPH0410443B2 JP58157305A JP15730583A JPH0410443B2 JP H0410443 B2 JPH0410443 B2 JP H0410443B2 JP 58157305 A JP58157305 A JP 58157305A JP 15730583 A JP15730583 A JP 15730583A JP H0410443 B2 JPH0410443 B2 JP H0410443B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- hair dye
- composition
- oxidative hair
- fatty
- 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.)
- Expired - Lifetime
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/361—Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/347—Phenols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Emergency Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Coloring (AREA)
Description
本発明は独特の流動学的性質をもつ水性酸化性
毛髪染料組成物に関する。
本発明の毛髪染料組成物はよい流動性と付着性
をもつ。
従来の酸化性毛髪染料組成物の物理的性質は一
般に染色操作の異なる段階に必要な流動性と妥協
している。酸化性毛髪染料組成物が毛髪に使われ
る場合それは流動性よく頭髪の1本1本の毛全部
を覆う様な適当な流動性のものでなければならな
い。反対に毛髪に使用後染料があまりさらさらし
ていれば染料は頭から流れてしまつて好ましくな
い。染料に粘性をもたせて後者の問題を防ごうと
すれば染料をつける際毛髪にうまく流れないであ
ろう。
出願人らは約3200乃至約10000センチポアズ
(cps)の低せん断割合(シエアレート)(8.5/
秒)粘度と約70乃至約150cpsの高せん断割合
(1370/秒)粘度および1インチより大きくない
付着流下距離(stay−put flow distance)をも
つ好ましい変動粘度特性をもつ酸化性毛髪染料組
成物を発見した。本発明の組成物は全組成物重量
を基準として約5乃至約10%の分子内炭素原子18
乃至22をもつ脂肪酸、上記脂肪酸を中和しかつ毛
髪染料組成物PHを8.5乃至11.5とするに十分なア
ルカリ化剤、約1.25乃至約5%の分子内炭素原子
12乃至22をもつ脂肪族アルコール、約1.5乃至約
6%の無水H2O2で表わした毛髪染料酸化剤およ
び約10乃至約15%のHLB約9乃至11.5をもつ少
なくも1のアルコキシル化アルキルフエノールを
含む。時に断らない限りパーセントはすべて重量
パーセントである。化学名はすべて化粧品香料協
会1982年出版のCFTA化粧品成分辞典に使われた
命名法によつて使用している。変助数は室温にお
けるものである。
故に本発明は著しい揺変性、即ちむしろ急傾斜
をもつせん断割合曲線の関数としての粘度をもつ
毛髪染料組成物を提供するものである。これは本
発明の基本組成物を含む毛髪染料組成物が高剪断
をうけた時、例えばそれをつける際撹拌した時と
その後しばらくその粘度が低いことを意味する。
これはそれを毛髪につける際流動性十分な流体と
なる。組成物を毛髪につけたあとそれは次第に粘
くなり毛からしたたつたり流れたりしない。多数
の市販毛髪染料組成物との比較試験は本発明によ
り製造した毛髪染料組成物の流動性のすぐれてい
ることを証明している。
乳化剤のHLBはアトラスケミカルインダスト
リーズ社出版のThe Atlas HLB Systemと題す
る冊子に記述されている処により決定される。
HLBとは親水性−親脂性平衡を表わす。この系
は1940年代後半アトラスケミカルインダストリー
ズによつて物質の乳化性の系統的表示方式として
導入された。各乳化剤はそのHLBという数値を
定められた。乳化剤はすべて親水性と親脂性の両
方を組合せる分子より成るので、この数値は各乳
化剤における親水性又は極性基と親脂性又は非極
性基の大きさと強さの平衡をいう。性質が親脂性
である乳化剤はHLB9以下であり、また親水性で
あるものはHLB11以上である。HLB9と11の間
のものは中間性と考えられる。
多数の乳化剤を混合した場合、混合物の合成
HLBは与えられた成分のパーセントとそのHLB
の積の算術的合計である。例えばアルコキシル化
アルキルフエノール(HLB13)とノンオキシノ
ール−4(HLB8.8)の等濃度混合物の場合えら
れる混合物のHLBは10.9である。他の適当する
アルコキシル化アルキルフエノール又はその混合
物は毛髪染料組成物の分野の平均的知識ある者に
は容易に明らかであろう。
酸化剤は本発明組成物の重要成分であるので、
また染髪分野で顕色剤組成物ともいわれる酸化剤
は毛髪染料中間体1又は2以上を含む組成物(染
髪分野でしばしば“テイント”(tint)という)
から離しておく必要があるので、また顕色剤およ
びテイント組成物は共に水溶液であるので、アル
コキシル化アルキルフエノール乳化剤の少なくと
も1部は顕色剤組成物に含まれているとよい。こ
れは顕色剤組成物とテイント組成物を使用前互い
に混合する場合の両者の混合を容易にする。
本発明に使わるC18−C22脂肪酸の例はステアリ
ン酸、ベヘニン酸、アラキジン酸、アラキドン
酸、オレイン酸、リノレイン酸又はそれらの混合
物、例えば天然産トール油酸がある。これらの酸
は飽和でも不飽和でもよい。
ラウリル、オレイル、ステアリル、イソステア
リル、セチル、ミリスチル、ベヒニルアルコール
等の様な種々のC12−C22脂肪族アルコールが本発
明に使用できる。これらのアルコールは飽和、不
飽和、直鎖又は分岐鎖構造をもつていてもよい。
アルカリ化剤は脂肪酸を中和しまた必要なアル
カリ性PHをつくるため毛髪保護組成物に普通使わ
れるどんな物質でもよく、水酸化アンモニウム、
モノエタノールアミン等がある。
酸化剤は過酸化水素で表わされるが、毛髪処理
組成物に使うに適した他の酸化剤、例えば過酸化
尿素の様な他の過酸化物も使用できる。特許明細
書全体に毛髪染料組成物について記述されている
のであるが、本発明も明細書と特許請求範囲をと
おし記述しているとおり発色する毛髪染料中間体
を必ずしも含まないおだやかな漂白剤含有を考え
ている。しかし通常主として毛髪漂白用組成物は
過酸化水素の様な酸化剤の外にパーコンパウンド
粉末の様な漂白ブースターを含む。しかし本発明
の便利な変動粘度特性はこの様な漂白ブースター
を組成物に加えてもえられないことがわかつた。
本発明組成物の流動性を比較的多数の市販酸化
性毛髪染料と比較した。比較結果を下記実施例中
に示している。市販の化合物はすべてある程度そ
の粘度へのせん断割合依存度を示すが、本発明組
成物程高せん断割合依存度を示すものはなかつ
た。故に従来の市販組成物配合において低せん断
割合において高粘度とするため(よい付着性をえ
るため)又は高せん断割合において低粘度とする
ため(よい流動性とするため)の両方ではないが
いづれかにトレイドオフ(tradeoff)が必要であ
つた。僅かの例外では市販組成物製造業者は一般
に低せん断割合において不十分な高粘度をえる犠
牲において高せん断割合において低粘度とするこ
とを選んでいる。粘度値のかなり鋭いせん断割合
依存度がせん断割合範囲の高端と低端両方におい
て理想粘度に到達させるので、本発明組成物の場
合このトレイドオフは必要ない。
実施例によればラベルにあげられた成分に基づ
いてこの比較に使われた市販酸化性毛髪染料製品
が多数あげられている。成分表は他国では必要な
いのでこの情報は米国で販売されている市販毛髪
染料にのみ利用できる。成分を利用できる市販酸
化性毛髪染料のいづれもが本発明の独特な組合せ
成分を含んでいない。
本発明による組成物および市販酸化性毛髪染料
組成物のせん断割合による粘度測定は市販組成物
の製造者が明らかに主として毛髪に染色組成物を
使用中よい流動性を目的としていることを示した
ので、更に一連の試験を行なつた。この試験にお
いて本発明による組成物と市販組成物の高粘度付
着性を比較した。各酸化性毛髪染料組成物を傾斜
板の上部に塗りつけ、5分後に各試料の流下距離
を測つた。この比較付着試験結果は下記実施例に
も示している。この結果は1市販毛髪染料組成物
(ポリカラークリームヘヤカラー45)のみが本発
明組成物と同じ付着性をもつことを示した。同じ
市販組成物の高せん断割合粘度データはしかし比
較的よくない流動性を示唆する比較的高粘度値を
示しまたもちろんこの市販組成物の場合のトレイ
ドオフがよりよい付着性のために低せん断割合に
おいて高粘度を与える方に重点がおかれたことを
示している。下に説明するとおり付着試験は更に
低せん断割合における高粘度は染料組成物のよい
付着性を必ずしも与えないことを示した。したが
つて組成物は8.5/秒の低せん断割合において約
3200乃至約10000cpsの粘度をもつことが必要な他
に付着試験において流下距離1インチ以内である
ことが更に必要である。
本発明による好ましい流動学的性質に寄与する
重要成分を決定するため多数の比較実験を行なつ
た。この比較実験は単に好ましい性質に寄与する
重要成分をきめるだけでなく、また低せん断粘度
値は組成物の付着性をある程度示すと予想される
が、傾斜板上の付着流下試験はより重要な性質で
なくても少なくも同等であるとした。故に高い低
せん断粘度は必ずしも傾斜板上の適当な付着結果
とはならない。
テイントベース組成物を基準として重量%で表
わした次の成分を含むテイントベースは比較基準
として役立つた。
ラウラミドDEA 3.0%
水酸化アンモニウム 8.7%
セチルアルコール 2.5
オレイン酸 12.0
ラウレツス−23 0.5
水を加えて 全量100とする。
実施例の顕色剤の等量をこの試験に用いた。ベ
ースは低せん断(8.5/秒)粘度5324cpsと高せん
断(1370/秒)粘度101cpsをもち、また付着流下
試験でそれは全く移動を示さなかつた。次表は比
較結果をまとめて示している。表の第1行は試料
と上記テイントベース組成物の間の差を示してい
る。
The present invention relates to aqueous oxidative hair dye compositions with unique rheological properties. The hair dye composition of the present invention has good flow and adhesion properties. The physical properties of conventional oxidative hair dye compositions are generally compromised by the fluidity required for the different stages of the dyeing operation. When the oxidative hair dye composition is used on the hair, it must be of suitable flowability so as to cover every single hair on the head. On the other hand, if the dye is too loose after use on the hair, the dye will run off the head, which is undesirable. If an attempt is made to prevent the latter problem by making the dye viscous, the dye will not flow properly into the hair when applied. Applicants have a low shear rate of about 3200 to about 10000 centipoise (cps) (8.5/
The oxidative hair dye composition has favorable variable viscosity characteristics with a high shear rate (1370/sec) viscosity of about 70 to about 150 cps and a stay-put flow distance of no greater than 1 inch. discovered. The compositions of the present invention contain from about 5 to about 10% molecular carbon atoms, based on the total composition weight.
a fatty acid having a molecular weight of from 1.25 to 22, sufficient alkalizing agent to neutralize the fatty acid and provide a hair dye composition pH of 8.5 to 11.5, and about 1.25 to about 5% intramolecular carbon atoms.
an aliphatic alcohol having an HLB of 12 to 22, about 1.5 to about 6% of an anhydrous H 2 O 2 hair dye oxidizing agent, and about 10 to about 15% of at least one alkoxylated alkyl having an HLB of about 9 to 11.5. Contains phenols. All percentages are by weight unless otherwise indicated. All chemical names are used according to the nomenclature used in the CFTA Dictionary of Cosmetic Ingredients published by the Cosmetic Fragrance and Fragrance Association in 1982. Variables are at room temperature. The present invention therefore provides hair dye compositions that have a marked thixotropy, ie a viscosity as a function of a rather steep shear rate curve. This means that when a hair dye composition comprising the base composition of the invention is subjected to high shear, for example when it is stirred during application, and for some time thereafter, its viscosity is low.
This results in a fluid that is fluid enough to apply it to the hair. After applying the composition to the hair, it gradually becomes sticky and does not drip or run from the hair. Comparative tests with a number of commercially available hair dye compositions demonstrate the superior flowability of the hair dye compositions prepared according to the present invention. The HLB of an emulsifier is determined as described in a booklet entitled The Atlas HLB System published by Atlas Chemical Industries.
HLB stands for hydrophilic-lipophilic equilibrium. This system was introduced by Atlas Chemical Industries in the late 1940s as a systematic representation of the emulsifying properties of substances. Each emulsifier was assigned a numerical value called its HLB. Since all emulsifiers are composed of molecules that combine both hydrophilic and lipophilic properties, this number represents a balance between the size and strength of the hydrophilic or polar groups and the lipophilic or non-polar groups in each emulsifier. Emulsifiers that are lipophilic in nature have an HLB of 9 or less, and those that are hydrophilic have an HLB of 11 or more. Those between HLB9 and 11 are considered intermediate. Synthesis of mixtures when a large number of emulsifiers are mixed
HLB is the percentage of a given ingredient and its HLB
is the arithmetic sum of the products of For example, in the case of a mixture of equal concentrations of alkoxylated alkylphenol (HLB 13) and nonoxynol-4 (HLB 8.8), the resulting mixture has an HLB of 10.9. Other suitable alkoxylated alkylphenols or mixtures thereof will be readily apparent to those of average skill in the art of hair dye compositions. Since the oxidizing agent is an important component of the composition of the present invention,
An oxidizing agent, also called a developer composition in the hair dyeing field, is a composition containing one or more hair dye intermediates (often referred to as a "tint" in the hair dyeing field).
Since the developer and the taint composition are both aqueous solutions, at least a portion of the alkoxylated alkylphenol emulsifier may be included in the developer composition. This facilitates mixing the developer composition and the taint composition when they are mixed together before use. Examples of C18 - C22 fatty acids for use in the present invention are stearic acid, behenic acid, arachidic acid, arachidonic acid, oleic acid, linoleic acid or mixtures thereof, such as naturally occurring tall oil acid. These acids may be saturated or unsaturated. A variety of C12 - C22 aliphatic alcohols can be used in the present invention, such as lauryl, oleyl, stearyl, isostearyl, cetyl, myristyl, behenyl alcohol, and the like. These alcohols may have a saturated, unsaturated, linear or branched structure. The alkalizing agent can be any substance commonly used in hair protection compositions to neutralize fatty acids and create the necessary alkaline pH, such as ammonium hydroxide,
Examples include monoethanolamine. Although the oxidizing agent is represented by hydrogen peroxide, other oxidizing agents suitable for use in hair treatment compositions can also be used, such as other peroxides, such as urea peroxide. Although the entire patent specification describes a hair dye composition, the present invention also contains a mild bleaching agent that does not necessarily contain a color-forming hair dye intermediate, as described throughout the specification and claims. thinking. Generally, however, hair bleaching compositions typically contain, in addition to an oxidizing agent such as hydrogen peroxide, a bleach booster such as Percompound powder. However, it has been found that the convenient variable viscosity properties of the present invention cannot be obtained by adding such bleach boosters to the composition. The flow properties of the compositions of the present invention were compared to a relatively large number of commercially available oxidative hair dyes. Comparison results are shown in the Examples below. Although all commercially available compounds exhibit some degree of shear rate dependence on their viscosity, none showed as high a shear rate dependence as the compositions of the present invention. Therefore, in conventional commercial composition formulations, either, but not both, to obtain high viscosity at low shear rates (to obtain good adhesion) or to obtain low viscosity at high shear rates (to obtain good flowability). A tradeoff was necessary. With few exceptions, commercial composition manufacturers generally choose to have low viscosities at high shear rates at the expense of insufficiently high viscosities at low shear rates. This trade-off is not necessary for the compositions of the invention since the fairly sharp shear rate dependence of the viscosity values allows ideal viscosities to be reached at both the high and low ends of the shear rate range. The examples list a number of commercially available oxidative hair dye products that were used in this comparison based on the ingredients listed on the label. This information is only available for commercial hair dyes sold in the United States, as ingredient lists are not required in other countries. None of the commercially available oxidative hair dyes available contain the unique combination of ingredients of this invention. Viscosity measurements by shear rate of compositions according to the invention and of commercially available oxidative hair dye compositions have shown that the manufacturers of commercially available compositions clearly primarily aim for good fluidity during use of the dyeing compositions on hair. , and conducted a series of further tests. In this test, the high viscosity adhesion properties of compositions according to the invention and commercially available compositions were compared. Each oxidative hair dye composition was applied to the upper part of the inclined plate, and after 5 minutes, the flow distance of each sample was measured. The results of this comparative adhesion test are also shown in the Examples below. The results showed that only one commercially available hair dye composition (Polycolor Cream Hair Color 45) had the same adhesion as the composition of the present invention. High shear rate viscosity data for the same commercial composition however shows relatively high viscosity values indicating relatively poor flow properties and of course the trade-off for this commercial composition is that at low shear rates for better adhesion This shows that emphasis was placed on providing high viscosity. Adhesion tests, as explained below, further showed that high viscosity at low shear rates does not necessarily give good adhesion of the dye composition. Therefore, at a low shear rate of 8.5/sec, the composition
In addition to having a viscosity of 3,200 to about 10,000 cps, it is also necessary to have a flow distance of less than 1 inch in an adhesion test. A number of comparative experiments were conducted to determine the key components contributing to the preferred rheological properties of the present invention. This comparative experiment not only determines the key components that contribute to favorable properties, and while low shear viscosity values are expected to indicate some degree of adhesion of the composition, the adhesion flow test on a tilted plate reveals more important properties. Even if it is not, it is at least equivalent. Therefore, high low shear viscosity does not necessarily result in proper adhesion on inclined plates. A taint base containing the following ingredients expressed in weight percent based on the taint base composition served as a comparison standard. Lauramid DEA 3.0% Ammonium hydroxide 8.7% Cetyl alcohol 2.5 Oleic acid 12.0 Lauretus-23 0.5 Add water to make total volume 100. Equivalent amounts of the developer of the example were used in this test. The base has a low shear (8.5/sec) viscosity of 5324 cps and a high shear (1370/sec) viscosity of 101 cps, and it showed no movement in the deposition flow test. The following table summarizes the comparison results. The first row of the table shows the differences between the samples and the taint base compositions described above.
【表】
アルコール
[Table] Alcohol
【表】
ソステアリン
アルコール
顕色剤成分として毛髪染料組成物に貢献する他
の重要成分を決定するため更に一連の比較試験を
行なつた。したがつて酸化剤は重要な成分であり
また毛髪染料組成物を基準として約10乃至15重量
%のHLB約9乃至約11.5をもつアルコキシル化
アルキルフエノールの存在も重要であるとわかつ
た。
下記実施例は本発明の実施態様を示すものであ
る。特に断らない限りパーセントはすべて実施例
の組成物の重量基準である。
実施例
(1) 次の組成物は淡褐色染色を与える酸化性毛髪
染料組成物の色成分である。
水酸化アンモニウム 8.7%
セチルアルコール 1.5
ステアリルアルコール 1.0
ラウラミドDEA3 3.0
オレイン酸 12.0
香 料 0.1
ラウレツス−23 0.5
フエニレンジアミド 0.27
N,Nビス(2−ヒドロキシエチル)p−フエ
ニレンジアミン硫酸塩 0.11
1−ナフトール 0.1
レゾルシノール 0.85
亜硫酸ナトリウム 0.1
エリソルビン酸 0.2
EDTA 0.05
水を加えて 全量100とする
色組成物は水酸化アンモニウム、2脂肪族ア
ルコール(セチルとステアリル)およびオレイ
ン酸を含んでおり、これらは本発明の組成物の
重要成分である。
(2) ブロンド色調を与える次の色組成物を製造し
た。
水酸化アンモニウム 9.0%
セチルアルコール 4.5
ラウラミドDEA3 3.0
オレイン酸 13.0
香 料 0.1
ラウレツス−23 0.5
p−フエニレンジアミン 0.06
N,Nビス(2−ヒドロキシエチル)p−フエ
ニレンジアミン硫酸塩 0.16
1−ナフトール 0.03
レゾルシノール 1.0
亜硫酸ナトリウム 0.1
エリソルビン酸 0.2
EDTA 0.05
水を加えて 全量を100とする
(3) 上記(1)又は(2)の色組成物と同時に使用するた
め次の顕色剤を製造した。
ノンオキシノール−9 10.0%
ノンオキシノール−4 10.0%
EDTA 0.02
過酸化水素50% 12.3
水を加えて 全量100とする
上記(1)または(2)の色組成物のいずれかと上記(3)
の顕色剤組成物の等容量部を混合して染髪組成物
を生成した。混合物を直接噴出孔から毛髪に応用
できるびんの中で振とうし又は2組成物を混合び
ん中で混合した後普通染髪において行なうとおり
混合物を応用ブラシユでつけることができる。
市販酸化性毛髪染料を本発明によつて製造した
組成物と比較する粘度測定をハーケロトヴイスコ
粘度計を用いて行なつた。結果を次表に示してい
る。粘度は低せん断割合8.5/秒および高せん断
割合1730/秒における各物質のセンチポアズ
(cps)で示した。上記(3)の顕色剤を使用した本発
明の場合を除いて組成物はすべて市販試料のそれ
ぞれの顕色剤組成物を使用した。Table: Sostearin Alcohol A further series of comparative tests were conducted to determine other important components that contribute to hair dye compositions as developer components. Therefore, the oxidizing agent is an important ingredient and the presence of an alkoxylated alkylphenol having an HLB of about 9 to about 11.5 in an amount of about 10 to 15% by weight based on the hair dye composition has also been found to be important. The following examples illustrate embodiments of the invention. All percentages are by weight of the example compositions unless otherwise noted. Example (1) The following composition is the color component of an oxidative hair dye composition that provides a tan coloring. Ammonium hydroxide 8.7% Cetyl alcohol 1.5 Stearyl alcohol 1.0 Lauramide DEA3 3.0 Oleic acid 12.0 Fragrance 0.1 Lauretus-23 0.5 Phenylenediamide 0.27 N,N bis(2-hydroxyethyl)p-phenylenediamine sulfate 0.11 1-naphthol 0.1 Resorcinol 0.85 Sodium sulfite 0.1 Erythorbic acid 0.2 EDTA 0.05 Add water to make a total volume of 100% The color composition contains ammonium hydroxide, di-aliphatic alcohols (cetyl and stearyl) and oleic acid, which are the compositions of the present invention. It is an important component of things. (2) The following color composition giving a blonde tone was prepared. Ammonium hydroxide 9.0% Cetyl alcohol 4.5 Lauramide DEA3 3.0 Oleic acid 13.0 Fragrance 0.1 Lauretus-23 0.5 p-phenylenediamine 0.06 N,N bis(2-hydroxyethyl) p-phenylenediamine sulfate 0.16 1-naphthol 0.03 Resorcinol 1.0 Sodium sulfite 0.1 Erythorbic acid 0.2 EDTA 0.05 Add water to make the total amount 100 (3) The following color developer was prepared for use at the same time as the color composition of (1) or (2) above. Nonoxynol-9 10.0% Nonoxynol-4 10.0% EDTA 0.02 Hydrogen peroxide 50% 12.3 Add water to make a total volume of 100 Either of the above color compositions (1) or (2) and the above (3)
A hair coloring composition was prepared by mixing equal parts of the developer composition. The mixture can be shaken in a bottle which can be applied directly to the hair through the spout or the two compositions can be mixed in a mixing bottle and the mixture can then be applied with an application brush as is normally done in hair dyeing. Viscosity measurements comparing commercially available oxidative hair dyes to compositions prepared according to the invention were made using a Herkerotwisko viscometer. The results are shown in the table below. Viscosity was expressed in centipoise (cps) for each material at a low shear rate of 8.5/sec and a high shear rate of 1730/sec. Except for the case of the present invention in which the color developer described in (3) above was used, all the compositions used were commercially available color developer compositions.
【表】【table】
【表】
本発明組成物と市販酸化性毛髪製品との比較付
着流下試験を60°角の傾斜硬厚紙上に各毛髪染料
組成物0.5gをつけて行なつた。5分後に各試料
の流下距離を測つた。種々の試料の流下距離を次
表にインチで表わした。市販酸化性染料の場合そ
の製品の顕色剤を使用した。本発明組成物の場合
実施例の(3)の顕色剤を用いた。市販試料のあとの
数字は色調名を表わしている。
試 料 流下距離(インチ)
実施例の(1)の色調成物 0
実施例の(2)の色調成物 0
ナイスンイージー 1.7
プレフアレンス9 1/2BB 2.7
エクセレンス6 2.8
ホートモードA 2.2
ミスクレアロルシヤンプー配合36 1.7
ミスクレアロルクリーム配合36 0.9
クレアレツセ206 4.3
コレストン800N 2.6
マジブロンド 1.8
ポリカラートナングスワツシエ18 3.3
ポリカラークリームヘアカラー45 0
よい付着流下性を示した最後の市販資料の場合
のこの試料の高せん断粘度データはこの製品配合
にあたり流下性を明らかに高粘度に妥協させてい
ることを示している。
米国内で販売されまた本明細書で比較用に使わ
れた市販製品の表示から次の組成が確認される。
プレフアレンス、テイント:アンモニア、オレ
イン酸、オレイルアルコール、コカミドDEA、
ポリグリセリル−4−オレイルエーテル、ポリグ
リセリル−2−オレイルエーテル、顕色剤:セテ
ス−2、オレアミドDEA、
ナイスンイージー、テイント:アンモニア、オ
レイン酸、オクトキシノール−1、ノンオキシノ
ール−4、コカミドDEA、顕色剤:ノンオキシ
ノール−9、ノンオキシノール−4、セチルアル
コール、ステアリルアルコール、
ミスクレアロルシヤンプー配合、テイント:ト
ール油脂肪酸、オクトキシノール−1、ノンオキ
シノール−4、リノールアミドDEA、顕色剤:
ノンオキシノール−9、ノンオキシノール−4、
セチルアルコール、ステアリルアルコール、
ミスクレアロルクリーム配合、テイント:アン
モニア、オレイン酸、ノンオキシノール−4、ノ
ンオキシノール−1、ラウリル硫酸ナトリウム、
顕色剤:水、
エクセレンス、テイント:アンモニア、トリエ
タノールアミン、ラウレス硫酸アンモニウム、パ
レス−15−9、パレス−15−3、顕色剤:セテス
−2、オレアミドDEA。
クレアレツセ、テイント:モノエタノールアミ
ン、オクトキシノール−1、ノンオキシノール−
9、リノールアミド−DEA、顕色剤:ノンオキ
シノール−9、セチルアルコール、ステアリルア
ルコール。Table: Comparative deposition and flow tests of the compositions of the present invention and commercially available oxidizing hair products were carried out on slanted hardboard paper at a 60° angle with 0.5 g of each hair dye composition. After 5 minutes, the flow distance of each sample was measured. The flow distances of the various samples are shown in the following table in inches. In the case of commercially available oxidative dyes, the developer of that product was used. In the case of the composition of the present invention, the color developer of Example (3) was used. The number after the commercially available sample represents the color tone name. Sample flow distance (inch) Color toning composition of Example (1) 0 Color toning composition of Example (2) 0 Nice Easy 1.7 Preference 9 1/2BB 2.7 Excellence 6 2.8 Hort Mode A 2.2 Misclare Lorci Formulation 36 1.7 Misclairol Cream Formulation 36 0.9 Claretsse 206 4.3 Koleston 800N 2.6 Magi Blonde 1.8 Polycolor Tongue Swatshie 18 3.3 Polycolor Cream Hair Color 45 0 This sample is the last commercially available material that showed good adhesion and flowability. The high shear viscosity data for this product indicate that flowability is clearly compromised by high viscosity in this product formulation. The following composition is identified from the labeling of commercial products sold in the United States and used herein for comparison. Preferences, taints: ammonia, oleic acid, oleyl alcohol, cocamide DEA,
Polyglyceryl-4-oleyl ether, polyglyceryl-2-oleyl ether, color developer: ceteth-2, oleamide DEA, nice-n-easy, taint: ammonia, oleic acid, octoxynol-1, nonoxynol-4, cocamide DEA , Color developer: Nonoxynol-9, Nonoxynol-4, Cetyl alcohol, Stearyl alcohol, Mixed with misclairol shampoo, Taint: Tall oil fatty acid, Octoxynol-1, Nonoxynol-4, Linolamide DEA , developer:
Nonoxynol-9, Nonoxynol-4,
Contains cetyl alcohol, stearyl alcohol, miscreal cream, taint: ammonia, oleic acid, nonoxynol-4, nonoxynol-1, sodium lauryl sulfate,
Color developer: Water, Excellence, Taint: Ammonia, triethanolamine, ammonium laureth sulfate, Pareth-15-9, Pareth-15-3, Color developer: Ceteth-2, Oleamide DEA. Clearess, Taint: Monoethanolamine, Octoxynol-1, Nonoxynol-
9. Linolamide-DEA, color developer: nonoxynol-9, cetyl alcohol, stearyl alcohol.
Claims (1)
脂肪酸、(b)上記脂肪酸を中和しかつ組成物のPHを
8.5〜11.5とするに十分なアルカリ化剤、(c)1.25〜
5%のC12-22脂肪族アルコール、(d)1.5〜6%の、
無水過酸化水素として表わした毛髪染料酸化剤、
および(e)10〜15%の、9〜11.5のHLBをもつア
ルコキシル化アルキルフエノールを含み上記の脂
肪酸、アルカリ化剤、脂肪族アルコール、毛髪染
料酸化剤およびアルコキシル化アルキルフエノー
ルのそれぞれの量が室温において組成物がせん断
割合8.5/秒において3200〜10000センチポアズの
粘度とせん断割合1370/秒において70〜150セン
チポアズの粘度をもちかつ2.54cm(1インチ)以
下の付着流下距離をもつ様な量であることを特徴
とする酸化性毛髪染料組成物。 2 脂肪酸が飽和又は不飽和であり、脂肪族アル
コールが飽和又は不飽和でありかつ直鎖又は分岐
鎖構造をもちまた上記組成物が少なくとも1酸化
性毛髪染料中間体を含む特許請求の範囲第1項に
記載の酸化性毛髪染料組成物。 3 脂肪酸がステアリン酸、ベヘニン酸、アラキ
ジン酸、アラキドニン酸、オレイン酸、リノレイ
ン酸およびトール油酸より成る群の少なくとも1
種である特許請求の範囲第2項に記載の酸化性毛
髪染料組成物。 4 脂肪酸アルコールがラウリル、オレイル、ス
テアリル、イソステアリル、セチル、ミリスチル
およびベヒニルアルコールより成る群の少なくも
1種である特許請求の範囲第2項に記載の酸化性
毛髪染料組成物。 5 アルコキシル化されたアルキルフエノールが
エトキシル化アルキルフエノールである特許請求
の範囲第2項に記載の酸化性毛髪染料組成物。 6 上記脂肪酸がステアリン酸、ベヘニン酸、ア
ラキジン酸、アラキドニン酸、オレイン酸、リノ
レイン酸およびトール油酸より成る群の少なくと
も1種であり、上記脂肪族アルコールがラウリ
ル、オレイル、ステアリル、イソステアリル、セ
チル、ミリスチルおよびベヒニルアルコールより
成る群の少なくとも1種であり、アルコキシル化
アルキルフエノールがエトキシル化ノニルフエノ
ールであり、かつ脂肪酸の中和とPH調節を水酸化
アンモニア使用により行う特許請求の範囲第1項
に記載の酸化性毛髪染料組成物。[Claims] 1. (a) 5 to 10% C 18-22 based on the total weight of the composition;
fatty acids, (b) neutralizes the above fatty acids and lowers the PH of the composition;
Sufficient alkalizing agent to give 8.5 to 11.5, (c) 1.25 to
5% C 12-22 aliphatic alcohol, (d) 1.5-6%,
hair dye oxidizing agent, expressed as anhydrous hydrogen peroxide;
and (e) 10 to 15% of an alkoxylated alkyl phenol with an HLB of 9 to 11.5, containing amounts of each of the above fatty acids, alkalizing agents, fatty alcohols, hair dye oxidizing agents, and alkoxylated alkyl phenols at room temperature. in such an amount that the composition has a viscosity of 3200 to 10000 centipoise at a shear rate of 8.5/sec, a viscosity of 70 to 150 centipoise at a shear rate of 1370/sec, and a deposition distance of less than 1 inch. An oxidative hair dye composition characterized by: 2. The fatty acid is saturated or unsaturated, the fatty alcohol is saturated or unsaturated and has a linear or branched structure, and the composition comprises at least one oxidative hair dye intermediate. The oxidative hair dye composition described in Section 1. 3. The fatty acid is at least one of the group consisting of stearic acid, behenic acid, arachidic acid, arachidonic acid, oleic acid, linoleic acid, and tall oil acid.
The oxidative hair dye composition according to claim 2, which is a species. 4. The oxidative hair dye composition according to claim 2, wherein the fatty acid alcohol is at least one member of the group consisting of lauryl, oleyl, stearyl, isostearyl, cetyl, myristyl, and behinyl alcohol. 5. The oxidative hair dye composition according to claim 2, wherein the alkoxylated alkylphenol is an ethoxylated alkylphenol. 6 The fatty acid is at least one member of the group consisting of stearic acid, behenic acid, arachidic acid, arachidonic acid, oleic acid, linoleic acid, and tall oil acid, and the aliphatic alcohol is lauryl, oleyl, stearyl, isostearyl, and cetyl. , myristyl, and behenyl alcohol, the alkoxylated alkylphenol is ethoxylated nonylphenol, and the neutralization of the fatty acid and the pH adjustment are performed by using ammonia hydroxide. Claim 1 The oxidative hair dye composition described in .
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41305582A | 1982-08-30 | 1982-08-30 | |
| US413055 | 1982-08-30 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3293971A Division JPH0653656B2 (en) | 1982-08-30 | 1991-08-22 | Package containing two containers of oxidative hair dye composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5989612A JPS5989612A (en) | 1984-05-23 |
| JPH0410443B2 true JPH0410443B2 (en) | 1992-02-25 |
Family
ID=23635635
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58157305A Granted JPS5989612A (en) | 1982-08-30 | 1983-08-30 | Acidic hair dye composition |
| JP3293971A Expired - Fee Related JPH0653656B2 (en) | 1982-08-30 | 1991-08-22 | Package containing two containers of oxidative hair dye composition |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3293971A Expired - Fee Related JPH0653656B2 (en) | 1982-08-30 | 1991-08-22 | Package containing two containers of oxidative hair dye composition |
Country Status (23)
| Country | Link |
|---|---|
| JP (2) | JPS5989612A (en) |
| KR (1) | KR900002335B1 (en) |
| AU (1) | AU562790B2 (en) |
| BE (1) | BE897616A (en) |
| BR (1) | BR8304675A (en) |
| CA (1) | CA1221914A (en) |
| CH (1) | CH654999A5 (en) |
| DE (1) | DE3329916C2 (en) |
| DK (1) | DK393283A (en) |
| ES (1) | ES525189A0 (en) |
| FI (1) | FI77369C (en) |
| FR (1) | FR2532174B1 (en) |
| GB (1) | GB2129447B (en) |
| GR (1) | GR81545B (en) |
| HK (1) | HK15989A (en) |
| IT (1) | IT1207979B (en) |
| MX (1) | MX158214A (en) |
| NL (1) | NL8302977A (en) |
| NO (1) | NO833042L (en) |
| NZ (1) | NZ205364A (en) |
| PT (1) | PT77261B (en) |
| SE (1) | SE461830B (en) |
| ZA (1) | ZA836137B (en) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3534471A1 (en) * | 1985-09-27 | 1987-04-02 | Henkel Kgaa | OXIDATION HAIR READING |
| DE3625916A1 (en) * | 1986-07-31 | 1988-02-04 | Wella Ag | OXIDATION HAIR COLORING AGENT BASED ON A GEL-SHAPED WEIGHT AND METHOD FOR COLORING HAIR |
| LU86899A1 (en) * | 1987-05-25 | 1989-01-19 | Oreal | PROCESS FOR DYEING KERATINIC FIBERS WITH OXIDATION DYES ASSOCIATED WITH IODIDE AND TINCTORIAL COMPOSITION USED |
| JPH01165513A (en) * | 1987-12-22 | 1989-06-29 | Hoou Kk | Thixotropic transparent hair dye composition |
| DE4005008C2 (en) * | 1990-02-19 | 1995-01-05 | Wella Ag | Oxidative hair colorant from a liquid color carrier mass and an emulsion-type, oxidant-containing composition and method for the oxidative dyeing of hair |
| DE19604932A1 (en) * | 1996-02-10 | 1997-08-14 | Wella Ag | Oxidation hair dye |
| US6187058B1 (en) * | 1998-05-20 | 2001-02-13 | Combe, Inc., | Low water no volatile organic compound hair lightener and dyeing composition |
| DE19905768A1 (en) * | 1999-02-11 | 2000-08-17 | Goldwell Gmbh | Pre-emulsion for hair color production contains fatty alcohol ethoxylate, oleic acid, ethanediol and/or propanediol distearate and glycerol stearate and/or sugar fatty acid ester |
| FR2833834B1 (en) * | 2001-12-21 | 2004-01-30 | Oreal | COMPOSITION FOR KERATIN FIBER OXIDATION STAIN COMPRISING OXYALKYLENE CARBOXYLIC ETHER ACID, MONO-OR POLY-GLYCEROL SURFACTANT AND UNSATURATED FATTY ALCOHOL |
| FR2833835B1 (en) | 2001-12-21 | 2004-01-30 | Oreal | COMPOSITION FOR THE OXIDATION STAIN OF KERATINOUS FIBERS COMPRISING AN OXYALKYLENE CARBOXYLIC ETHER ACID, A MONO-OR POLY-GLYCEROL SURFACTANT AND A NON-IONIC OXYALKYLENE SURFACTANT |
| JP2004196812A (en) * | 2004-02-03 | 2004-07-15 | Kao Corp | Hair dye composition |
| EP2512603A2 (en) * | 2009-12-18 | 2012-10-24 | The Procter & Gamble Company | Foam oxidative hair colorant composition |
| EP2512685B1 (en) * | 2009-12-18 | 2015-07-22 | The Procter and Gamble Company | Personal care composition foaming product |
| CN107361508B (en) | 2011-03-21 | 2020-11-03 | 卡拉莱特有限公司 | Custom Dyeing Systems |
| US9316580B2 (en) | 2011-03-21 | 2016-04-19 | Coloright Ltd. | Systems for custom coloration |
| US10302495B2 (en) | 2013-09-26 | 2019-05-28 | Coloright Ltd. | Hair reader, dispenser device and related systems and methods |
| CN106572736B (en) | 2014-04-27 | 2020-01-31 | 卡拉莱特有限公司 | Method and device for customized hair coloring |
| WO2015166340A2 (en) | 2014-04-27 | 2015-11-05 | Coloright Ltd. | Apparatus and method for analyzing hair and/or predicting an outcome of a hair-coloring treatment |
| US10292482B2 (en) | 2017-01-06 | 2019-05-21 | Coloright Ltd. | Hair-holder, hair-reader comprising the same, and methods for optically acquiring data from hair |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7002938A (en) * | 1969-05-16 | 1970-11-18 | ||
| BE746268A (en) * | 1969-07-31 | 1970-08-20 | Gillette Co | TWO-PART PACKAGING FOR HAIR DYE |
| US3823231A (en) * | 1971-04-20 | 1974-07-09 | F Bucaria | Hair bleach containing a thiocyanate catalyst |
| FR2428437A2 (en) * | 1974-05-16 | 1980-01-11 | Oreal | Hair cosmetics for dyeing, bleaching or permanent waving - contg. quaternised poly:amine-urea polymers |
| AU7076774A (en) * | 1974-07-04 | 1976-01-08 | Kintex Inc | Bleach |
| DK161009C (en) * | 1977-09-07 | 1991-10-28 | Oreal | PREPARATIONS FOR COLORING HER OXIDATION COLORS AND BASIS |
| JPS5512407A (en) * | 1978-07-12 | 1980-01-29 | Nippon Seiko Kk | Method of compensating error in measuring circle of arc and meter with compensator |
| US4402698A (en) * | 1979-12-13 | 1983-09-06 | L'oreal | Hair-dyeing process involving protection of the scalp |
-
1983
- 1983-08-19 DE DE3329916A patent/DE3329916C2/en not_active Expired - Lifetime
- 1983-08-19 ZA ZA836137A patent/ZA836137B/en unknown
- 1983-08-22 MX MX198465A patent/MX158214A/en unknown
- 1983-08-23 NZ NZ205364A patent/NZ205364A/en unknown
- 1983-08-24 NO NO833042A patent/NO833042L/en unknown
- 1983-08-25 FI FI833044A patent/FI77369C/en not_active IP Right Cessation
- 1983-08-25 NL NL8302977A patent/NL8302977A/en not_active Application Discontinuation
- 1983-08-26 CA CA000435400A patent/CA1221914A/en not_active Expired
- 1983-08-26 FR FR8313791A patent/FR2532174B1/en not_active Expired
- 1983-08-26 AU AU18473/83A patent/AU562790B2/en not_active Expired
- 1983-08-26 GB GB08323014A patent/GB2129447B/en not_active Expired
- 1983-08-26 ES ES525189A patent/ES525189A0/en active Granted
- 1983-08-29 BR BR8304675A patent/BR8304675A/en unknown
- 1983-08-29 DK DK393283A patent/DK393283A/en not_active Application Discontinuation
- 1983-08-29 PT PT77261A patent/PT77261B/en not_active IP Right Cessation
- 1983-08-29 BE BE211419A patent/BE897616A/en unknown
- 1983-08-29 SE SE8304673A patent/SE461830B/en not_active IP Right Cessation
- 1983-08-30 JP JP58157305A patent/JPS5989612A/en active Granted
- 1983-08-30 GR GR72333A patent/GR81545B/el unknown
- 1983-08-30 KR KR1019830004040A patent/KR900002335B1/en not_active Expired
- 1983-08-30 CH CH4754/83A patent/CH654999A5/en not_active IP Right Cessation
- 1983-08-30 IT IT8322700A patent/IT1207979B/en active
-
1989
- 1989-02-23 HK HK159/89A patent/HK15989A/en not_active IP Right Cessation
-
1991
- 1991-08-22 JP JP3293971A patent/JPH0653656B2/en not_active Expired - Fee Related
Also Published As
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