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JP2007126384A - Pretreatment agent for acid hair dye - Google Patents

Pretreatment agent for acid hair dye Download PDF

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Publication number
JP2007126384A
JP2007126384A JP2005319353A JP2005319353A JP2007126384A JP 2007126384 A JP2007126384 A JP 2007126384A JP 2005319353 A JP2005319353 A JP 2005319353A JP 2005319353 A JP2005319353 A JP 2005319353A JP 2007126384 A JP2007126384 A JP 2007126384A
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Prior art keywords
hair
pretreatment agent
hair dye
dye
acidic
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Japanese (ja)
Inventor
Kazuya Shibata
和也 芝田
Emiko Kawada
恵美子 河田
Masaaki Uemura
雅明 植村
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Shiseido Co Ltd
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Shiseido Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a pretreatment agent for an acid hair dye, obtained by targeting improved dye-affinity and fastness, and hardly causing damage of the hair. <P>SOLUTION: The pretreatment agent for the acid hair dye contains urea and benzyl alcohol formulated therewith, and has pH 5.0-11.0. A copolymer composition comprising a dimethyldiallylammonium chloride and acrylamide, and having 2,000-40,000 average molecular weight is preferably compounded therewith in the pretreatment agent for the acid hairdye. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

本発明は、酸性染毛料を適用するに当たってその染色性及び堅牢性の向上を目的とした毛髪の損傷が少ない酸性染毛料用前処理剤に関する。   TECHNICAL FIELD The present invention relates to a pretreatment agent for acidic hair dyes that causes less hair damage for the purpose of improving dyeability and fastness when applying the acidic hair dye.

周知のとおり、酸性染毛料(ヘアマニキュア)は、二液型の酸化染毛料より手軽に用いることができるため、市場のニーズが高まっているが、染色性や染まりの堅牢性の点でさらなる向上が求められている。
酸性染毛料の染色力と堅牢性を向上させるために酸性染毛料を適用する前に用いる前処理剤が知られている。従来の酸性染毛料用前処理剤は、ベンジルアルコールを含有させて酸性にする技術が知られているが、染色力を向上させる効果が非常に弱い。
また、酸性染毛料用前処理剤にアルカリ剤と有機溶剤を配合しpH7.5〜11.0としさらに還元剤を配合したものが知られており(特許文献1)、染毛剤に尿素を配合することで堅牢性に優れた染毛料を得る試みもなされている(特許文献2)。
特開2000−169344号公報 特開平09−278636号公報
As is well known, acidic hair dyes (hair manicure) can be used more easily than two-component oxidative hair dyes, so the market needs are increasing, but further improvements are made in terms of dyeability and dyeing fastness. Is required.
In order to improve the dyeing power and fastness of an acidic hair dye, a pretreatment agent used before applying the acidic hair dye is known. Conventional acid hair dye pretreatment agents are known to be made acidic by containing benzyl alcohol, but the effect of improving dyeing power is very weak.
In addition, it is known that an alkaline agent and an organic solvent are blended in a pretreatment agent for acidic hair dye to have a pH of 7.5 to 11.0 and a reducing agent is blended (Patent Document 1), and urea is added to the hair dye. Attempts have also been made to obtain a hair dye excellent in fastness by blending (Patent Document 2).
JP 2000-169344 A JP 09-278636 A

しかしながら、特許文献1記載のアルカリ剤と有機溶剤を配合し、pH7.5〜11.0である前処理剤組成物は染色性及び堅牢性の向上効果が必ずしも十分ではなく、また還元剤を配合することで当該効果は上がるものの、毛髪の損傷がかなり大きくなってしまう。一方、特許文献2の染毛料は、酸性染料を用いる場合にはpHを4以下にすることで染色毛の堅牢性は上がるが毛髪の損傷が大きくなり、また尿素が分解し安定して配合できないため、尿素による向上効果を得ることはできない。   However, the pretreatment agent composition containing the alkali agent and organic solvent described in Patent Document 1 and having a pH of 7.5 to 11.0 is not necessarily sufficient in improving the dyeability and fastness, and contains a reducing agent. Although this effect is improved, hair damage is considerably increased. On the other hand, in the case of using an acid dye, the hair dye of Patent Document 2 increases the fastness of the dyed hair by adjusting the pH to 4 or less, but damage to the hair increases, and urea is decomposed and cannot be stably blended. Therefore, the improvement effect by urea cannot be obtained.

本発明の目的は、後に適用する酸性染毛料の染色性及び堅牢性を向上させる効果に優れていると共に、毛髪の損傷が少ない酸性染毛料用前処理剤を提供することにある。 The objective of this invention is providing the pretreatment agent for acidic hair dyes which is excellent in the effect which improves the dyeing property and fastness of the acidic hair dye applied later, and there is little damage to hair.

前記事情に鑑み、本発明者等が鋭意検討を行った結果、尿素とベンジルアルコールを配合し還元剤や酸性染料を実質的に含まないことで毛髪の損傷が少なく、またpHを5.0〜11.0に調整することで尿素を安定に配合した、染色性及び堅牢性向上効果に優れた前処理剤が得られることを見出した。また、さらに塩化ジメチルジアリルアンモニウムクロライドとアクリルアミドとからなる平均分子量が2000〜40000の共重合体組成物を配合することにより、後に適用する酸性染毛料の染色性及び堅牢性がより向上することを見出し、本発明を完成するに至った。   In view of the above circumstances, as a result of intensive studies by the present inventors, there is little damage to hair by blending urea and benzyl alcohol and containing substantially no reducing agent or acidic dye, and the pH is 5.0 to By adjusting to 11.0, it discovered that the pre-processing agent which mix | blended urea stably and was excellent in the dyeing | staining property and fastness improvement effect was obtained. Further, it has been found that the dyeing property and fastness of an acidic hair dye to be applied later are further improved by further blending a copolymer composition having an average molecular weight of 2,000 to 40,000 consisting of dimethyldiallylammonium chloride and acrylamide. The present invention has been completed.

すなわち、本発明は、尿素とベンジルアルコールが配合されており、かつ、pH5.0〜11.0であり、還元剤や酸性染料を実質的に含まないことを特徴とした酸性染毛料用前処理剤である。 That is, the present invention is a pretreatment for an acidic hair dye characterized in that urea and benzyl alcohol are blended, has a pH of 5.0 to 11.0, and does not substantially contain a reducing agent or an acidic dye. It is an agent.

前記酸性染毛料用前処理剤において、尿素の配合量は、0.1〜30質量%、ベンジルアルコールの配合量が0.1〜30質量%である。
また、前記酸性染毛料用前処理剤において、還元剤及び/又は酸性染料を実質的に含まない。
In the pretreatment agent for acidic hair dye, the compounding amount of urea is 0.1 to 30% by mass, and the compounding amount of benzyl alcohol is 0.1 to 30% by mass.
Moreover, in the said pretreatment agent for acidic hair dye, a reducing agent and / or an acidic dye are not included substantially.

また、前記酸性染毛料用前処理剤において、さらに塩化ジメチルジアリルアンモニウムクロライドとアクリルアミドとからなる平均分子量が2000〜40000の共重合体組成物を配合する。 In the pretreatment agent for acidic hair dye, a copolymer composition having an average molecular weight of 2,000 to 40,000 consisting of dimethyl diallyl ammonium chloride and acrylamide is further blended.

本発明の酸性染毛料用前処理剤は、毛髪の損傷が少なく、後に適用する酸性染毛料の染色性、堅牢性を十分に向上させることができる。   The pretreatment agent for acidic hair dye of the present invention has little damage to hair and can sufficiently improve the dyeability and fastness of the acidic hair dye to be applied later.

以下、本発明の実施の形態について詳述する。   Hereinafter, embodiments of the present invention will be described in detail.

<尿素>
尿素は保水力に優れており、毛髪内の水素結合を効果的に切断することができる。酸性染毛料は通常pH2〜4に調整されており、毛髪に塗布してもわずかに毛髪が膨潤する程度である。しかし、前処理剤に尿素を配合することによって、毛髪が膨潤しやすくなり、酸性染料の毛髪内への浸透性が増大する。また、酸性染料は水溶性であるため、毛髪内で尿素が保水することにより、透過ルートが十分に確保され、スムーズに浸透される。その結果、毛髪内へ多くの酸性染料が浸透することにより、染色力が向上し、深く浸透することにより、堅牢性が向上する。
本発明での尿素の配合量は、0.1〜30質量%であるが、好ましくは1.0〜20質量%、さらに好ましくは3〜10質量%である。30質量%以上配合すると、安定性が悪くなる傾向がある。
<Urea>
Urea has excellent water retention ability, and can effectively break hydrogen bonds in hair. Acid hair dyes are usually adjusted to a pH of 2 to 4, and the hair swells slightly even when applied to the hair. However, by adding urea to the pretreatment agent, the hair tends to swell and the penetrability of the acid dye into the hair increases. Further, since the acid dye is water-soluble, the urea is retained in the hair, so that a permeation route is sufficiently ensured and smoothly penetrated. As a result, the dyeing power is improved by penetration of many acidic dyes into the hair, and the fastness is improved by deep penetration.
The blending amount of urea in the present invention is 0.1 to 30% by mass, preferably 1.0 to 20% by mass, and more preferably 3 to 10% by mass. When 30 mass% or more is blended, the stability tends to deteriorate.

<ベンジルアルコール>
本発明に使用されるベンジルアルコールは、組成物中に0.1〜30質量%、好ましくは1〜15.0質量%、さらに好ましくは2〜8質量%配合される。ベンジルアルコールを組成物中に含むことで後に適用する酸性染毛料の染着性を向上させることができる。
<Benzyl alcohol>
The benzyl alcohol used for this invention is 0.1-30 mass% in a composition, Preferably it is 1-15.0 mass%, More preferably, 2-8 mass% is mix | blended. By including benzyl alcohol in the composition, it is possible to improve the dyeability of an acidic hair dye to be applied later.

<塩化ジメチルジアリルアンモニウムクロライドとアクリルアミドとからなる平均分子量が2000〜40000の共重合体組成物>(以下、「共重合体(A)」という)
本発明に使用する共重合体(A)は、塩化ジメチルジアリルアンモニウムクロライド(以下DADMACと略す場合がある)と、アクリルアミド(以下AAmと略す場合がある)とを、水とイソプロピルアルコール(以下IPAと略す場合がある)の混合溶媒中にて重合開始剤を用いて常法により共重合して得られる共重合体であり、その平均分子量は2000〜40000のカチオン性共重合体である。共重合体のモノマー組成比はDADMAC:AAmが20:80〜60:40が好ましく、下記の構成単位からなるランダム共重合体である。精製した共重合体(A)を適当な濃度で溶解した水溶液として使用しても良いし、純分が100%になるまで乾燥して使用しても良い。
<Copolymer composition having an average molecular weight of 2,000 to 40,000 consisting of dimethyldiallylammonium chloride and acrylamide> (hereinafter referred to as “copolymer (A)”)
The copolymer (A) used in the present invention comprises dimethyldiallylammonium chloride (hereinafter sometimes abbreviated as DADMAC), acrylamide (hereinafter sometimes abbreviated as AAm), water and isopropyl alcohol (hereinafter referred to as IPA). A copolymer obtained by copolymerization by a conventional method using a polymerization initiator in a mixed solvent, which is a cationic copolymer having an average molecular weight of 2000 to 40000. The monomer composition ratio of the copolymer is preferably DADMAC: AAm of 20:80 to 60:40, and is a random copolymer composed of the following structural units. The purified copolymer (A) may be used as an aqueous solution in which it is dissolved at an appropriate concentration, or may be used after being dried until the pure content becomes 100%.

Figure 2007126384
Figure 2007126384

共重合体(A)の平均分子量は、ゲルパーミエーションクロマトグラフィー(以下GPCと略す)による重量平均分子量(以下、Mwと略す)で、その平均分子量が2000〜40000である。好ましくは、3000〜33000程度である。以下にGPCの測定条件を示す。
<GPCの測定条件>
カラム: OHpak SB−804HQ、
OHpak SB−803HQ、
OHpak SB−802HQ、(いずれも昭和電工株式会社製)
カラム温度 :40℃、
検出器 :RI、
溶媒 :0.25M酢酸+0.05M食塩(pH=3.5)、
流速 :0.7ml/分、
試料濃度 :0.5%、
注入量 :50μl、
標準 :プルラン、
(昭和電工株式会社製;Shodex STANDARD P−82)
The average molecular weight of the copolymer (A) is a weight average molecular weight (hereinafter abbreviated as Mw) by gel permeation chromatography (hereinafter abbreviated as GPC), and the average molecular weight is 2000 to 40000. Preferably, it is about 3000-33000. The measurement conditions for GPC are shown below.
<GPC measurement conditions>
Column: OHpak SB-804HQ,
OHpak SB-803HQ,
OHpak SB-802HQ (all manufactured by Showa Denko KK)
Column temperature: 40 ° C.
Detector: RI,
Solvent: 0.25M acetic acid + 0.05M sodium chloride (pH = 3.5),
Flow rate: 0.7 ml / min,
Sample concentration: 0.5%
Injection volume: 50 μl,
Standard: Pullulan,
(Made by Showa Denko; Shodex STANDARD P-82)

なお、従来から化粧料に配合されている、DADMACとAAmの共重合体の重量平均分子量は、数10万のオーダーを有する分子量の大きいものである。例えば、MEポリマー09W(東邦化学工業社製)の重量平均分子量は約45万であり、本発明に使用する平均分子量2000〜40000の共重合体(A)とは極めて大きく異なる高分子量の共重合体である。   In addition, the weight average molecular weight of the copolymer of DADMAC and AAm conventionally blended in cosmetics has a large molecular weight having an order of several hundred thousand. For example, the weight average molecular weight of ME polymer 09W (manufactured by Toho Chemical Industry Co., Ltd.) is about 450,000, and the copolymer weight of the high molecular weight is very different from the copolymer (A) having an average molecular weight of 2000 to 40000 used in the present invention. It is a coalescence.

本発明における前記共重合体の配合量は、特に限定されないが、通常0.01〜50質量%であり、製品形態上好ましくは0.1〜20質量%、さらに好ましくは1〜10質量%である。   The blending amount of the copolymer in the present invention is not particularly limited, but is usually 0.01 to 50% by mass, preferably 0.1 to 20% by mass, and more preferably 1 to 10% by mass on the product form. is there.

本発明においては還元剤及び/又は酸性染料を実質的に含まないことを特徴とする。「実質的に含まない」とは、組成物中に全く含まないか、含んだとしても、0.01重量%以下であり、還元剤、酸性染料が、毛髪への還元効果や染色効果の機能を発揮しない程度を意味する。なお、酸性染料の場合、組成物基剤への着色を目的とする程度の微量(0.01重量%以下)は含まれていてもよい。   The present invention is characterized in that it contains substantially no reducing agent and / or acid dye. “Substantially free” means that it is not contained in the composition at all, or even if it is contained, it is 0.01% by weight or less, and the reducing agent and acid dye function to reduce or dye the hair. It means the degree of not exhibiting. In addition, in the case of an acid dye, a trace amount (0.01 weight% or less) of the grade aiming at coloring to a composition base may be contained.

なお、本発明の効果を損ねない範囲で、粘度調整剤、色剤、香料、光沢付与剤等を配合させることができる。
本発明の処理剤の剤型は、ローション(液状)、ミスト状、ゲル状、フォーム状、スプレー状等のさまざまな剤型を取ることができる。適用方法としては、本発明の処理剤を毛髪に塗布し、水洗しタオルドライした後に通常の酸性染毛料を適用すればよい。なお、毛髪への塗布後、数分間室温あるいは加温して放置することにより、より毛髪への薬剤浸透が促され、本願の効果がより高まる傾向がある。
In addition, a viscosity modifier, a colorant, a fragrance | flavor, a gloss imparting agent, etc. can be mix | blended in the range which does not impair the effect of this invention.
The dosage form of the treatment agent of the present invention can take various dosage forms such as lotion (liquid), mist, gel, foam, spray and the like. As an application method, the treatment agent of the present invention is applied to hair, washed with water and towel-dried, and then a normal acidic hair dye may be applied. It should be noted that, after application to the hair, leaving it for several minutes at room temperature or warming further promotes the penetration of the drug into the hair and tends to enhance the effect of the present application.

本発明について以下に実施例を挙げてさらに詳述するが、本発明はこれにより何ら限定されるものではない。配合量は特記しない限り、その成分が配合される系に対する質量%で示す。   The present invention will be described in more detail with reference to the following examples, but the present invention is not limited thereto. Unless otherwise specified, the blending amount is expressed in mass% with respect to the system in which the component is blended.

「共重合体(A)の合成例1」
温度計、還流冷却器及び攪拌機を備えた容量3リットルのガラスフラスコに水834g、IPA1172g仕込み、60℃に加温した。次いで、AAm173g(2.4モル)と65%DADMAC水溶液233g(0.9モル)、水92gの混合溶液と、20%過硫酸ナトリウム水溶液97g、20%重亜硫酸ナトリウム水溶液211gとを、それぞれ別々の滴下漏斗から6時間かけて、攪拌下に反応器に滴下した。滴下終了後さらに6時間反応液を60℃に保持し、重合を完結させた。重合終了後、攪拌を止め、二相分離した下相溶液を分取し、50%IPA水溶液1400gで洗浄、静置した後分相し、下相溶液を分取した。この洗浄操作をさらにもう1回行い、下相の含ポリマー溶液を得た。
これに、等量の水を加え、減圧下、80℃、減圧下でIPAを留去した。得られたポリマー水溶液のGPCを測定した結果、Mw3,000であった。
<GPCの測定条件>
カラム OHpak SB−804HQ
OHpak SB−803HQ
OHpak SB−802HQ
(いずれも昭和電工株式会社製)
カラム温度 :40℃
検出器 :RI
溶媒 :0.25M酢酸+0.05M食塩(pH=3.5)
流速 :0.7ml/分
試料濃度 :0.5%
注入量 :50μl
標準 :プルラン
(昭和電工株式会社製;Shodex STANDARD P−82)
"Synthesis example 1 of copolymer (A)"
A glass flask having a capacity of 3 liters equipped with a thermometer, a reflux condenser and a stirrer was charged with 834 g of water and 1172 g of IPA and heated to 60 ° C. Next, a mixed solution of AAm 173 g (2.4 mol), 65% DADMAC aqueous solution 233 g (0.9 mol) and water 92 g, 20% sodium persulfate aqueous solution 97 g, and 20% sodium bisulfite aqueous solution 211 g were separately added. It was dripped at the reactor under stirring from the dropping funnel over 6 hours. After completion of the dropping, the reaction solution was kept at 60 ° C. for 6 hours to complete the polymerization. After completion of the polymerization, stirring was stopped, the lower phase solution separated into two phases was separated, washed with 1400 g of 50% IPA aqueous solution, allowed to stand, and then phase-separated to separate the lower phase solution. This washing operation was performed once more to obtain a polymer solution containing the lower phase.
An equal amount of water was added thereto, and IPA was distilled off under reduced pressure at 80 ° C. under reduced pressure. It was Mw 3,000 as a result of measuring GPC of the obtained polymer aqueous solution.
<GPC measurement conditions>
Column OHpak SB-804HQ
OHpak SB-803HQ
OHpak SB-802HQ
(Both made by Showa Denko KK)
Column temperature: 40 ° C
Detector: RI
Solvent: 0.25M acetic acid + 0.05M sodium chloride (pH = 3.5)
Flow rate: 0.7 ml / min Sample concentration: 0.5%
Injection volume: 50 μl
Standard: Pull Run
(Made by Showa Denko; Shodex STANDARD P-82)

「実施例〜4、比較例1〜4」
表1に示す組成で酸性染毛料用前処理剤を常法(増粘剤を精製水に溶解した後、各種成分を添加して均一に混合し、pHを調整した。)にて調整し、染色性、堅牢性、毛髪の損傷度、組成物の安定性について評価した。なお、それぞれの評価は次の方法で実施した。
"Examples 4 to 4, Comparative Examples 1 to 4"
Adjust the pretreatment agent for acidic hair dye with the composition shown in Table 1 by a conventional method (after dissolving the thickener in purified water, add various components and mix uniformly, and adjust the pH). The dyeability, fastness, hair damage degree, and composition stability were evaluated. In addition, each evaluation was implemented with the following method.

<染色性試験>
白髪の毛束に過剰量の前処理用組成物を塗布して(毛髪2gに対して組成物を15g)25℃で5分間放置した。5分経過後、水洗して前処理剤組成物を洗い流し、タオルドライした。この毛束に酸性染毛料(RX−T アクティブカラー ナチュラルブラウン・資生堂プロフェッショナル株式会社製)を過剰量(15g)塗布し、30℃で10分間放置した。10分経過後、シャンプーで2回洗浄し、毛束を乾燥させた。毛束の染まりは前処理剤を使用しないときの染まりと比較し、非常に良く染まっていて前処理剤の染色性向上効果が高い場合の評価を◎、やや染まりが良くて前処理剤の染色性向上効果がやや高い場合の評価を○、染まりに差が感じられず前処理剤の染色性向上効果がない場合の評価を△、染まりが悪く前処理剤が染色性を阻害した場合の評価を×とした。
<Dyeability test>
An excessive amount of the pretreatment composition was applied to the white hair bundle (15 g of the composition with respect to 2 g of hair) and left at 25 ° C. for 5 minutes. After 5 minutes, it was washed with water to wash away the pretreatment composition and towel-dried. An excessive amount (15 g) of acidic hair dye (RX-T Active Color Natural Brown, manufactured by Shiseido Professional Co., Ltd.) was applied to this hair bundle and left at 30 ° C. for 10 minutes. After 10 minutes, the hair bundle was dried by shampooing twice. Compared with the dyeing when the pretreatment agent is not used, the hair bundle dyeing is very well dyed and the pretreatment agent is highly effective in improving the dyeability. Evaluation when the effect of improving the dyeability is slightly high, evaluation when the difference in dyeing is not felt and the effect of improving the dyeing property of the pretreatment agent is △, evaluation when the pretreatment agent is poor in dyeing and the dyeing property is inhibited Was marked with x.

<堅牢性試験>
染色性の評価試験で使用した毛束を2%ラウリル硫酸ナトリウム水溶液に浸漬し、30℃で30分間振とうした。その後、水洗し、風乾させた。このとき前処理剤を使用していない毛束の色落ちの程度と比較して、色落ちが非常に少ない場合の評価を◎、色落ちがやや少ない場合の評価を○、色落ちの程度に差がない場合の評価を△、色落ちが悪く比較している毛束より染まりが薄くなっている場合の評価を×とした。
<Robustness test>
The hair bundle used in the dyeability evaluation test was immersed in a 2% aqueous sodium lauryl sulfate solution and shaken at 30 ° C. for 30 minutes. Thereafter, it was washed with water and allowed to air dry. At this time, compared with the degree of color fading of the hair bundle not using the pretreatment agent, the evaluation when the color fading is very small is ◎, the evaluation when the color fading is slightly small is ○, the degree of color fading The evaluation when there was no difference was Δ, and the evaluation when the dyeing was lighter than the hair bundles being compared was bad, and the evaluation was x.

<毛髪損傷度試験>
島津製作所製のAUTOGRAPH(AGS−H)を用いて毛髪の強度を測定し、損傷の程度を評価した。この実験には同一人の健康毛を使用し、同じ資料で10回測定し平均した。前処理剤で処理(過剰量を塗布して25℃で5分間放置後水洗)した毛髪が処理前と強度に差がない場合の評価を○、強度がやや低下した場合の評価を△、著しく強度が低下した場合の評価を×とした。
<Hair damage test>
The strength of the hair was measured using AUTOGRAPH (AGS-H) manufactured by Shimadzu Corporation, and the degree of damage was evaluated. In this experiment, healthy hair of the same person was used, and the measurement was averaged 10 times using the same data. ○ When the hair treated with the pretreatment agent (applied excessive amount and left at 25 ° C for 5 minutes and then washed with water) has no difference in strength from that before the treatment, ○, evaluation when the strength is slightly reduced The evaluation when the strength was reduced was evaluated as x.

<組成物の安定性試験>
前処理剤組成物を樹脂容器およびスクリュー管に充填し、3ヶ月間室温で静置後、外観の観察とpHの測定を行い、製造直後と比較してほぼ変化がない場合の評価を○、やや変化があった場合の評価を△、かなり変化があった場合の評価を×とした。
<Composition stability test>
Fill the resin container and screw tube with the pretreatment agent composition, leave it at room temperature for 3 months, observe the appearance and measure the pH, and evaluate when there is almost no change compared to immediately after production, The evaluation when there was a slight change was indicated by Δ, and the evaluation when there was a considerable change was indicated by ×.

Figure 2007126384
Figure 2007126384


実施例5:
尿素 0.5
ベンジルアルコール 3.0
MEポリマーDAM(3000)
(品番・東邦化学工業株式会社製。共重合体(A)の7%水溶液) 15.0
ジプロピレングリコール 2.0
2−ヒドロキシ−n−カプリル酸 1.0
ヒドロキシエチルセルロース 3.0
ダイヤフォーマーZ732
(品番・三菱化学株式会社製) 1.0
n−メチルピロリドン 1.0
ショ糖脂肪酸エステル 0.1
プロシアニジン 0.5
d−リモネン 0.5
アンモニア水 pH10に調整
香料 適量
精製水 100部調整
合計 100.0

Example 5:
Urea 0.5
Benzyl alcohol 3.0
ME polymer DAM (3000)
(Product number: Toho Chemical Co., Ltd. 7% aqueous solution of copolymer (A)) 15.0
Dipropylene glycol 2.0
2-Hydroxy-n-caprylic acid 1.0
Hydroxyethyl cellulose 3.0
Diamond former Z732
(Part number, manufactured by Mitsubishi Chemical Corporation) 1.0
n-Methylpyrrolidone 1.0
Sucrose fatty acid ester 0.1
Procyanidin 0.5
d-limonene 0.5
Ammonia water Adjusted to pH 10 Fragrance Appropriate amount Purified water 100 parts Adjusted total 100.0

実施例6:
尿素 2.0
ベンジルアルコール 1.0
MEポリマーDAM(3000) 0.01
エタノール 5.0
没食子酸プロピル 0.5
リン酸ジセチル 1.0
セタノール 8.0
流動パラフィン 0.5
パルミチン酸イソプロピル 3.0
塩化ステアリルトリメチルアンモニウム 3.0
シリル化加水分解大豆タンパク 1.0
アルギニン 0.1
ピネン 1.0
乳酸 適量
乳酸ナトリウム pH7に調整
香料 適量
精製水 100部調整
合計 100.0
Example 6:
Urea 2.0
Benzyl alcohol 1.0
ME polymer DAM (3000) 0.01
Ethanol 5.0
Propyl gallate 0.5
Dicetyl phosphate 1.0
Cetanol 8.0
Liquid paraffin 0.5
Isopropyl palmitate 3.0
Stearyltrimethylammonium chloride 3.0
Silylated hydrolyzed soy protein 1.0
Arginine 0.1
Pinene 1.0
Lactic acid Appropriate amount Sodium lactate adjusted to pH 7 Perfume proper amount Purified water 100 parts Adjusted total 100.0

実施例7:
尿素 20.0
ベンジルアルコール 10.0
キサンタンガム 0.1
カルボキシビニルポリマー 3.0
ベンジルオキシエタノール 2.0
トコフェロール 0.1
γ−ヘキサノラクトン 5.0
α−オレフィンオリゴマー 1.0
セテス−10リン酸 0.5
ヘキサン酸 0.5
タンニン酸 0.5
グリコール酸 2.0
リン酸水素二ナトリウム pH5に調整
香料 適量
精製水 100部調整
合計 100.0
Example 7:
Urea 20.0
Benzyl alcohol 10.0
Xanthan gum 0.1
Carboxyvinyl polymer 3.0
Benzyloxyethanol 2.0
Tocopherol 0.1
γ-hexanolactone 5.0
α-olefin oligomer 1.0
Ceteth-10 phosphate 0.5
Hexanoic acid 0.5
Tannic acid 0.5
Glycolic acid 2.0
Disodium hydrogen phosphate adjusted to pH 5 Fragrance appropriate amount Purified water 100 parts Adjusted total 100.0


実施例8:
尿素 8.0
ベンジルアルコール 3.0
MEポリマーDAM(3000) 5.0
セタノール 11.0
プロピレングリコール 3.0
エタノール 5.0
ジメチコン 1.5
アミノプロピルジメチコン 0.5
オクタン酸セチル 5.0
L−グルタミン酸ナトリウム 0.5
レシチン 0.1
ポリオキシエチレンオレイルエーテル 2.0
ステアリン酸グリセリル 0.5
塩化ステアリルトリメチルアンモニウム 2.0
酒石酸 0.1
クエン酸ナトリウム pH6に調整
香料 適量
精製水 100部調整
合計 100.0


Example 8:
Urea 8.0
Benzyl alcohol 3.0
ME polymer DAM (3000) 5.0
Cetanol 11.0
Propylene glycol 3.0
Ethanol 5.0
Dimethicone 1.5
Aminopropyl dimethicone 0.5
Cetyl octanoate 5.0
Sodium L-glutamate 0.5
Lecithin 0.1
Polyoxyethylene oleyl ether 2.0
Glyceryl stearate 0.5
Stearyltrimethylammonium chloride 2.0
Tartaric acid 0.1
Sodium citrate pH 6 adjusted fragrance appropriate amount purified water 100 parts adjusted total 100.0

Claims (4)

尿素とベンジルアルコールとが配合されており、かつ、pH5.0〜11.0であることを特徴とする酸性染毛料用前処理剤。   A pretreatment agent for acidic hair dyes, which contains urea and benzyl alcohol and has a pH of 5.0 to 11.0. 請求項1記載の酸性染毛料用前処理剤において、尿素の配合量が0.1〜30質量%、ベンジルアルコールの配合量が0.1〜30質量%であることを特徴とする酸性染毛料用前処理剤。   The pretreatment agent for acidic hair dye according to claim 1, wherein the compounding amount of urea is 0.1 to 30% by mass and the compounding amount of benzyl alcohol is 0.1 to 30% by mass. Pre-treatment agent. 請求項1又は2に記載の酸性染毛料用前処理剤において、還元剤及び/又は酸性染料を実質的に含まないことを特徴とする酸性染毛料用前処理剤。   The pretreatment agent for acidic hair dye according to claim 1 or 2, wherein the pretreatment agent for acidic hair dye contains substantially no reducing agent and / or acidic dye. 請求項1乃至3のいずれかに記載の酸性染毛料用前処理剤において、さらに塩化ジメチルジアリルアンモニウムクロライドとアクリルアミドとからなる平均分子量が2000〜40000の共重合体組成物を配合することを特徴とする酸性染毛料用前処理剤。 The acidic hair dye pretreatment agent according to any one of claims 1 to 3, further comprising a copolymer composition comprising dimethyldiallylammonium chloride and acrylamide having an average molecular weight of 2000 to 40000. Pretreatment agent for acidic hair dye.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7896932B2 (en) 2007-10-12 2011-03-01 Kao Corporation Non-oxidative hair dye composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7896932B2 (en) 2007-10-12 2011-03-01 Kao Corporation Non-oxidative hair dye composition

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