阅读说明：本技术 毛发染色用制剂 (Preparation for hair dyeing ) 是由 赵诚昱 徐兪晶 于 2020-01-31 设计创作，主要内容包括：本发明涉及一种在确保碱性或直接染料的稳定性的同时提高碱性或直接染料的附着性的毛发染色用制剂。本发明的毛发染色用制剂即使不包含导致过敏和刺激的氧化染毛剂,也具有仅用碱性或直接染毛剂就能提供优异的染毛力和颜色保持力的效果。(The present invention relates to a hair dyeing preparation which ensures the stability of a basic or direct dye and improves the adhesion of the basic or direct dye. The preparation for hair dyeing of the present invention has an effect of providing excellent hair dyeing power and color retention with only an alkaline or direct hair dyeing agent even if it does not contain an oxidative hair dyeing agent causing allergy and irritation.)

1. A hair dye preparation characterized by comprising,

the hair-dyeing preparation comprises: a first agent comprising a basic dye (basic dye) or a direct dye (direct dye); and a second agent comprising an alkaline agent or an alkaline reducing agent,

said first and second agents are contained separately,

the first agent and the second agent are mixed or coated on each other immediately before use,

the pH when the first and second agents are mixed or applied overlappingly is 9 to 14.

2. The preparation for hair coloring according to claim 1, wherein said first agent comprises both a basic dye and a direct dye.

3. The preparation for hair dyeing according to any one of the preceding claims, characterized in that the preparation for hair dyeing contains substantially no oxidative hair dye.

4. The hair coloring preparation according to any one of the preceding claims, which contains substantially no oxidizing agent.

5. A preparation for dyeing hair according to any of the preceding claims characterized in that the pH of the first agent is 4 to 9.

6. A preparation for dyeing hair according to any of the preceding claims characterized in that the pH of the first agent is 4 to 7.5.

7. A hair dyeing preparation according to any one of the preceding claims, characterized in that said alkaline agent is an amine compound and/or an inorganic compound.

8. The hair coloring preparation according to any one of the preceding claims, wherein the difference in color (Δ E) of the hair before and after dyeing, measured using LabSacn XE of a colorimeter HunterLab for color measurement, is 25 or more after dyeing the hair with the hair coloring preparation.

Technical Field

The present application claims priority based on korean application No. 10-2019-0013471, published on 2/1/2019, korean application No. 10-2019-0129800, published on 10/18/2019, and korean application No. 10-2020-0011366, published on 1/30/2020, and all the contents disclosed in the description and drawings of the related applications are incorporated herein by reference.

The present invention relates to a preparation for dyeing hair comprising a basic or direct dye. More specifically, the present invention relates to a hair dyeing preparation and a dye set (kit) for improving the adhesion of a basic or direct dye while ensuring the stability of the basic or direct dye.

Background

Hair dyes for hair dyeing generally used are represented by oxidation hair dyes mainly using p-phenylenediamine or its derivatives and aminophenols. The hair dye using the oxidation hair dye is composed of the following components: a first agent composed of an oxidation dye and a second agent containing an oxidizing agent for color development and decolorization of hair by oxidative condensation reaction of the oxidation dye, and hydrogen peroxide is mainly used as the oxidizing agent. The hair dye agent containing the oxidation dye has the advantages of excellent color retention after dyeing hair and realization of multiple colors.

However, the oxidation dye used in the oxidation hair dye is known as a causative substance of allergy and irritation because the color is expressed by an oxidative condensation reaction between the oxidation dye and hydrogen peroxide, unlike a general dye, and hydrogen peroxide contained in the second agent is also a strong irritant substance. Therefore, many people who use the oxidative hair dye complain of various symptoms such as skin irritation, acne, rash, edema, respiratory disorder, etc. in use or after use.

On the other hand, as a dye for hair dyeing in which the fear of such allergy and irritation is remarkably reduced, a Direct dye (Direct dye) and a Basic dye (Basic dye, Cationic dye) are used in a product for hair dyeing. Most products to which such dyes are applied are products that do not use an oxidizing agent, mainly used in fashion products of red, blue, yellow, etc., and are products used after hair is decolorized with a decolorizing agent before use. On the other hand, when used as a product for covering white hair, there is a problem that satisfactory results are difficult to obtain because the hair-dyeing effect is remarkably reduced.

The reason is that, compared with oxidation dyes in which a dye precursor (intermediate) and a coupler (toner) penetrate deep into hair and develop color by condensation, basic dyes having a relatively large molecular weight hardly penetrate into the interior of normal hair of the cuticle layer, and dye hair in a form in which basic dyes having cationic properties are attached to the surface of hair with anions, but there is a limit to the extent of attachment to the surface, and when shampoo is used for washing after use, the basic dyes attached to hair can be easily shed by anionic surfactants contained in the shampoo, and thus it is difficult to obtain an excellent effect on a product for covering white hair. The direct dye may also penetrate into the hair, but has a problem in that it is relatively difficult to penetrate deep into the hair and fix it, and it is easily removed by washing with shampoo.

In order to solve these problems, a technique of adjusting the pH of a base color dye solution containing a basic reducing agent to 7.5 to 9 to improve the penetration of the dye, and then applying a catechin aqueous solution and irradiating far infrared rays has been developed, but it has the following problems: the storage stability is low and the dyeing process is complicated, so that there is a limit in practical productization.

Throughout this specification, reference is made to a number of documents and their citations are identified. The disclosures of the cited documents are incorporated by reference in their entirety into this specification in order to more clearly describe the state of the art to which this invention pertains and the contents of this invention.

Disclosure of Invention

Technical subject

The present inventors have made an effort to solve the problem that the desired color developing effect and color retention cannot be obtained without including an oxidative hair dye. As a result, they have revealed that even if an oxidative hair dye causing allergy and irritation is not contained, an excellent hair dyeing power and color retention can be provided only by an alkaline hair dye, and have completed the present invention.

Accordingly, an object of the present invention is to provide a dyeing preparation which solves the above problems while using a basic dye with significantly reduced anxiety of allergy and irritation.

Other objects and advantages of the present invention will be further apparent from the following detailed description of the invention, claims and drawings.

Means for solving the problems

An aspect of the present invention is to provide a hair-dyeing preparation comprising: a first agent comprising a basic dye (basic dye) or a direct dye (direct dye) and a second agent comprising an alkaline agent or a basic reducing agent. That is, it is characterized by comprising (i) a basic dye or a direct dye and (ii) an alkaline agent or a basic reducing agent, respectively, in two formulations different from each other.

The inventors of the present invention have revealed that the reason why a good dyeing effect cannot be exhibited with the conventional hair dye comprising a basic dye or a direct dye is due to a decrease in hair adhesion of the dye or the dye and the basic dye are contained in a mixed form, and have constituted the formulation of the present invention so as to be able to solve the problem.

Therefore, in the present invention, the first agent and the second agent may be separately contained, and the first agent and the second agent may be used by mixing or overlapping application immediately before use, and the pH when the first agent and the second agent are mixed or overlapped application may be 9 to 14.

The basic dye (basic dye or cationic dye) used in the present invention is a dye having an amino group or a substituted amino group in a molecule and being converted into a cation in an aqueous solution, and conventionally known basic dyes can be used without particular limitation. Basic dyes become cationic in aqueous solution and therefore dye by ionic binding to the negative (minus) portion of the keratin on the hair surface. Specific examples thereof include basic blue 7(c.i.42595), basic blue 16(c.i.12210), basic blue 22(c.i.61512), basic blue 26(c.i.44045), basic blue 99(c.i.56059), basic blue 117, basic violet 10(c.i.45170), basic violet 14(c.i.42515), basic brown 16(c.i.12250), basic brown 17(c.i.12251), basic red 2(c.i.50240), basic red 12 (c.i.07048), basic red 22(c.i.11055), basic red 51, basic red 76(c.i.12245), basic red 118(c.i.12251:1), basic orange 31, basic yellow 28 (c.i.054), basic yellow 57(c.i.12719), basic yellow 87, basic black 2(c.i.11825), and the like. These may be used alone, or 2 or more of them may be used in combination. However, not limited thereto, in general, all dyes widely known as basic dyes may be used.

According to the present inventors' findings, the basic or direct dye is more stable as it approaches neutrality (pH 4-9, more preferably pH 4-7.5), and if the pH is lower or higher than this range, the dye is decomposed in the storage tube to show a color different from the original color or lose the color. Thus, the basic or direct dye should be included separately from the second agent comprising the base or basic reducing agent, and preferably mixed with the second agent comprising the base or basic reducing agent or applied to the hair sequentially prior to use to enhance the coloring effect.

As the alkaline agent contained in the second agent of the present invention, in general, all alkaline agents widely used in cosmetics can be used, and can be used without particular limitation. For example, sodium hydroxide, potassium hydroxide, ethanolamine, diethanolamine, ammonia, ammonium carbonate, triethanolamine, aminomethylpropanol, tromethamine, and the like can be used, and one or more kinds thereof can be mixed and used. In addition, a similar effect can be obtained by using an alkaline reducing agent such as thioglycolates, inorganic sulfites, or the like without particular limitation.

In a preferred embodiment, the alkaline agent contained in the above-mentioned second agent may be an amine compound, for example, ethanolamine, diethanolamine, ammonia, ammonium carbonate, triethanolamine, aminomethylpropanol, tromethamine, or the like, and in this case, may have more excellent dyeing properties than in the case of containing an inorganic alkaline agent such as sodium hydroxide, potassium hydroxide, or the like.

The above first agent of the present invention may use a direct dye (direct dye) instead of the basic dye. In addition, the first agent may contain both a basic dye and a direct dye.

The direct dye is also referred to as HC dye, and is a dye having a known "HC" as a prefix, and since it is a dye having a small molecular diameter, it penetrates into the hair and dyes the hair by hydrogen bonding or intermolecular attraction. Specific examples thereof include, for example, HC blue No.2, HC blue No.8, HC orange No.1, HC orange No.2, HC red No.1, HC red No.3, HC red No.7, HC red No.8, HC red No.10, HC red No.11, HC red No.13, HC red No.16, HC violet No.2, HC yellow No.5, HC yellow No.6, HC yellow No.7, HC yellow No.9, and HC yellow No. 12. These may be used alone, or 2 or more of them may be used in combination. However, not limited thereto, in general, all dyes widely known as direct dyes may be used.

The hair-coloring preparation of the present invention may contain substantially no oxidative hair-coloring agent and/or oxidizing agent in both of the first agent and the second agent.

Here, the term "substantially not containing" may be that the relevant component is completely absent, or that the relevant component is hardly contained so that the effect is to the extent that it may be the same as in the case where the relevant component is completely absent. In other words, a formulation that "does not substantially contain" an ingredient or element may still substantially contain such items so long as there is no measurable effect. Unless otherwise indicated, the term "substantially free" means 1 wt% or less, 0.5 wt% or less, or 0.3 wt% or less, preferably 0.1 wt% or less, 0.05 wt% or less, or 0.03 wt% or less, more preferably 0.01 wt% or less, relative to the total content of formulation ingredients.

The oxidation dye precursor is a concept containing one or more oxidation dye precursors which are usually developed after oxidation, and examples of the oxidation dye precursors include p-phenylenediamine, p-toluylenediamine (para-phenylenediamine), 2-chloro-p-phenylenediamine, 2, 3-dimethyl-p-phenylenediamine, 2, 6-diethyl-p-phenylenediamine, 2, 5-dimethyl-p-phenylenediamine, N-diethyl-p-phenylenediamine, N-dipropyl-p-phenylenediamine, 4-amino-N, N-diethyl-3-methylaniline, N-bis (β -hydroxyethyl) -p-phenylenediamine, 4-amino-N, N-bis (β -hydroxyethyl) -3-methylaniline, and the like, Dyes of p-phenylenediamine series such as 4-amino-3-chloro-N, N-bis (. beta. -hydroxyethyl) -aniline, 2-. beta. -hydroxyethyl-p-phenylenediamine, 2-fluoro-p-phenylenediamine, 2-isopropyl-p-phenylenediamine, N- (. beta. -hydroxypropyl) -p-phenylenediamine, 2-hydroxymethyl-p-phenylenediamine, N-dimethyl-3-methyl-p-phenylenediamine, N- (. beta.,. gamma. -dihydroxypropyl) -p-phenylenediamine, N- (4' -aminophenyl) -p-phenylenediamine, N-phenyl-p-phenylenediamine, and 2-. beta. -hydroxyethoxy-p-phenylenediamine, or acid salts thereof, p-aminophenol, 4-amino-3-methylphenol, p-phenylenediamine, and mixtures thereof, A dye of p-aminophenol series such as 4-amino-3-fluorophenol, 4-amino-3-hydroxymethylphenol, 4-amino-2-methylphenol, 4-amino-2-hydroxymethylphenol, 4-amino-2-methoxymethylphenol, 4-amino-2-aminomethylphenol, 4-amino-2- (. beta. -hydroxyethylaminomethyl) phenol, 4-amino-2-fluorophenol or the like or an acid salt thereof, a dye of o-aminophenol series such as 2-aminophenol, 2-amino-5-methylphenol, 2-amino-6-methylphenol, 5-acetylamino-2-aminophenol or the like or an acid salt thereof, and the like, and as a dye containing other heterocyclic rings such as 2, pyridine derivatives such as 5-diaminopyridine, pyrimidine derivatives such as 2,4,5, 6-tetraaminopyrimidine and 4-hydroxy-2, 5, 6-triaminopyrimidine, and pyrazole derivatives such as 4, 5-diamino-1-methylpyrazole, 3, 4-diaminopyrazole and 4, 5-diamino-1- (4' -chlorobenzyl) pyrazole. Examples of the oxidizing agent for oxidizing the oxidation dye precursor include hydrogen peroxide, urea peroxide, alkali metal bromates, perborates, persulfates, and the like.

In a preferred embodiment of the present invention, the first agent has a neutral pH and the second agent has a basic pH.

As described above, in the present invention, in order to enhance the hair attachment effect of known relatively safe basic dyes and/or direct dyes, which are composed of a first agent containing one or more of basic dyes and direct dyes mixed or contained alone and a second agent containing an alkaline agent, it is possible to secure dye stability in a neutral pH region for several basic dyes and direct dyes. Here, the neutral pH means a pH of 4 to 9, preferably 4 to 7.5, and there is a disadvantage that it is difficult to ensure long-term stability of the dye due to hydrolysis or the like at a relatively high or low pH (more than 9 and less than 4) for basic dyes and direct dyes.

Further, when the basic dye is stored together with hydrogen peroxide at a low pH (for example, less than pH2 to 4), there is a problem that the basic dye is decomposed by an oxidation reaction of hydrogen peroxide. In addition, in the case of a basic dye or a direct dye, the lower the pH, the lower the solubility in water, and therefore the dye may be precipitated over time for a long period of time.

The alkaline pH of the second agent means exceeding pH7, and means alkaline to the extent that the pH of the first agent and the second agent after mixing can reach at least 7, preferably the pH after mixing can reach 9 to 14, more preferably the pH after mixing can reach 10 to 14.

As described above, when the pH of the mixed solution is adjusted to the alkaline condition, there is an advantage that the dyeing effect of the basic dye and/or the direct dye can be more strongly improved. Under alkaline conditions, the cationic dye strongly adheres to the hair surface through ionic bonds, and under alkaline conditions, the cuticle on the hair surface softens and swells, allowing the direct dye or the basic dye to easily penetrate into the hair, thereby having an effect of significantly enhancing the dyeing effect and also being effective in maintaining the dyed color.

Specifically, a basic dye having a cationic property in the aqueous solution phase is bonded to the surface of hair having an anionic property or penetrates into the inside, but the basic dye has a high molecular weight and therefore is difficult to easily penetrate or attach to hair in a large amount. The present inventors have revealed that, when dyeing is carried out under alkaline conditions, the binding force between the hair surface and the basic dye is increased, the hair cuticle is swollen by the alkaline component, the basic dye is more likely to penetrate into the hair cuticle, and the surface area to which the basic dye can bind is increased, thereby enhancing the dyeing effect. Thereafter, if a weakly acidic shampoo is used, the cuticle on the hair surface is finished, so that the basic dye introduced into the interior is not easily shed.

The hair dyeing preparation of the present invention is superior to available commercial products in color development and color retention after dyeing. Currently, commercial products using basic dyes generally have a color difference value (Δ E) of less than 25, and most of the dyed basic dyes are stripped from hair after about 1-2 shampooings.

On the other hand, the hair color difference value (Δ E) before and after dyeing, measured using LabSacn XE of HunterLab as a colorimeter for color measurement after dyeing hair with the hair dyeing preparation of the present invention, is 25 or more. A range in which the color difference value (Δ E) of the hair is 25 or more means a range including a color difference value of, for example, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50 or more. More preferably, the color difference value (Δ Ε) measured before/after dyeing using the formulation of the present invention may be from 30 to 50.

The color difference value can be calculated by measuring the coordinate values of L, a, b shown by the hue marks in the CIE 1976L a b color space according to the following calculation formula.

ΔE＝{(ΔL*)²+(Δa*)²+(Δb*)²}^1/2

The preparation for hair dyeing of the present invention can be used by mixing the first agent and the second agent immediately before application to hair, and can also be used as follows: the first dose may be applied to the hair and the second dose may be applied in an overlapping manner, or the second dose may be applied to the hair and the first dose may be applied in an overlapping manner. As described above, even if the first agent containing the dye is first applied to the hair and then the second agent containing the alkaline agent is applied in an overlapping manner or in reverse order, since the pH condition at the time of use is alkaline, the dyeing effect is excellent, which is similar to the mixed use.

Drawings

FIG. 1 shows the results of the evaluation of staining.

FIG. 2 shows the results of evaluation of hair-dyeing power at each pH.

Fig. 3 shows the results of evaluating the hair-dyeing ability according to the kind of alkaline agent.

Fig. 4 shows the results of performing color retention evaluation according to pH.

Fig. 5 shows the results of color retention evaluation when repeated washing was performed.

Fig. 6 shows the results of performing color retention evaluation according to repeated washing and pH.

Fig. 7 shows the results of adjusting the contents of the first dose of the preparation for dyeing to pH3, pH7, and pH10, storing the same, and then mixing the same with the second dose immediately before dyeing to evaluate the dyeing effect (dyeing target color: brown).

Detailed Description

Hereinafter, the present invention will be described in more detail by examples. These examples are only for more specifically describing the present invention, and it is apparent to those of ordinary skill in the art to which the present invention pertains that the scope of the present invention is not limited to these examples.

Examples

The substances and reagents used in this example were purchased and used from cosmetic raw material manufacturers and commercial suppliers, and the contents of the markers in the examples were based on weight%.

I. Preparation of a preparation for dyeing hair

(1) Example 1.

1 part of agent: mixing with cream mainly containing cetearyl alcohol, adding alkaline brown 16, alkaline blue 99, and HC blue 16 as dye components to make total amount of cream 1%, and making total amount of benzyl alcohol and glycerol below 5%.

2, preparation: the content of ethanolamine as an alkaline agent was adjusted and dosed so that the cream based on cetearyl alcohol reached pH7 when mixed with the first dose at 1: 1.

(2) Example 2.

1 part of agent: mixing with cream mainly containing cetearyl alcohol, adding alkaline brown 16, alkaline blue 99, and HC blue 16 as dye components to make total amount of cream 1%, and making total amount of benzyl alcohol and glycerol below 5%.

2, preparation: the content of ethanolamine as an alkaline agent was adjusted and dosed so that the cream mainly comprising cetearyl alcohol reached pH8 when mixed with the first agent at 1: 1.

(3) Example 3.

1 part of agent: mixing with cream mainly containing cetearyl alcohol, adding alkaline brown 16, alkaline blue 99, and HC blue 16 as dye components to make total amount of cream 1%, and making total amount of benzyl alcohol and glycerol below 5%.

2, preparation: the content of ethanolamine as an alkaline agent was adjusted and dosed so that the cream mainly comprising cetearyl alcohol reached pH9 when mixed with the first agent at 1: 1.

(4) Example 4.

1 part of agent: mixing with cream mainly containing cetearyl alcohol, adding alkaline brown 16, alkaline blue 99, and HC blue 16 as dye components to make total amount of cream 1%, and making total amount of benzyl alcohol and glycerol below 5%.

2, preparation: the content of ethanolamine as an alkaline agent was adjusted and dosed so that the cream mainly comprising cetearyl alcohol reached pH10 when mixed with the first agent at 1: 1.

(5) Example 5.

1 part of agent: mixing with cream mainly containing cetearyl alcohol, adding alkaline brown 16, alkaline blue 99, and HC blue 16 as dye components to make total amount of cream 1%, and making total amount of benzyl alcohol and glycerol below 5%.

2, preparation: the content of ethanolamine as an alkaline agent was adjusted and dosed so that the cream mainly comprising cetearyl alcohol reached pH11 when mixed with the first agent at 1: 1.

(6) Example 6.

1 part of agent: mixing with cream mainly containing cetearyl alcohol, adding alkaline brown 16, alkaline blue 99, and HC blue 16 as dye components to make total amount of cream 1%, and making total amount of benzyl alcohol and glycerol below 5%.

2, preparation: the cream based on cetearyl alcohol was adjusted and dosed to reach pH12 when the cream was mixed with the first dose at 1:1 as an alkaline agent.

(7) Example 7.

1 part of agent: mixing with cream mainly containing cetearyl alcohol, adding alkaline brown 16, alkaline blue 99, and HC blue 16 as dye components to make total amount of cream 1%, and making total amount of benzyl alcohol and glycerol below 5%.

2, preparation: the cream based on cetearyl alcohol was adjusted and dosed to reach pH13 when the cream was mixed with the first dose at 1:1 as an alkaline agent.

(8) Example 8.

1 part of agent: mixing with cream mainly containing cetearyl alcohol, adding alkaline brown 16, alkaline blue 99, and HC blue 16 as dye components to make total amount of cream 1%, and making total amount of benzyl alcohol and glycerol below 5%.

2, preparation: the cream based on cetearyl alcohol is adjusted and dosed to reach ph13.5 when mixed with the first dose in a ratio of 1:1 as an alkaline agent.

(9) Example 9.

1 part of agent: mixing with cream mainly containing cetearyl alcohol, adding alkaline brown 16, alkaline blue 99, and HC blue 16 as dye components to make total amount of cream 1%, and making total amount of benzyl alcohol and glycerol below 5%.

2, preparation: the cream based on cetearyl alcohol was adjusted and dosed to reach pH11 when the content of aminomethyl propanol as an alkaline agent was adjusted and dosed such that the first dose was mixed at 1: 1.

(10) Example 10.

1 part of agent: mixing with cream mainly containing cetearyl alcohol, adding alkaline brown 16, alkaline blue 99, and HC blue 16 as dye components to make total amount of cream 1%, and making total amount of benzyl alcohol and glycerol below 5%.

2, preparation: the cream based on cetearyl alcohol was adjusted and dosed to reach pH11 when the cream was mixed with the first dose at 1:1 as an alkaline agent.

(11) Example 11.

1 part of agent: mixing with cream mainly containing cetearyl alcohol, adding alkaline brown 16, alkaline blue 99, and HC blue 16 as dye components to make total amount of cream 1%, and making total amount of benzyl alcohol and glycerol below 5%.

2, preparation: it is prepared by adjusting and adding potassium hydroxide as an alkaline agent in such an amount that the cream based on cetearyl alcohol reaches pH11 when mixed with the first agent at a ratio of 1: 1.

(12) Comparative example 1.

1 part of agent: in a cream mainly containing cetearyl alcohol, and adding as dye components, alkali brown 16, alkali blue 99, and HC blue 16 in a total amount of 0.5% of the cream, and in a total amount of benzyl alcohol and glycerin of 5% or less, and prepared using aminomethylpropanol and aqueous citric acid so that the pH is 6.

The cream mainly containing cetearyl alcohol used in examples and comparative examples is a preparation obtained by appropriately blending the components of cetearyl alcohol, oleyl alcohol, polyoxyethylene cetyl ether (polyoxyyethylene cethylether), mineral oil, ethylene glycol stearate, cocamide MEA, and the like.

Experimental example II

1. Evaluation of staining

The following two preparations were used for evaluation of staining, and the results are shown in fig. 1. BM-W-A of BeAULAX, Japan, was used as the hair for dyeing, and LabSacn XE of HunterLab was used as the colorimeter for color measurement.

Composition a (composition of comparative example 1): general hair dyeing compositions using basic and direct dyes (pH6)

Composition B (composition of example 5): mixed composition comprising a first agent of basic and direct dyes and a second agent of base (pH11)

As seen from the graph of fig. 1, a is a general hair dyeing product using basic and direct dyes, B is a product in which a first agent containing a dye and a second agent containing an alkaline agent are mixed just before use, and from the result of measuring a change value Δ E of color by a color difference meter from a strand of hair for dyeing (white hair) dyed with a and B, it can be confirmed that there is a significant change in color to the effects of the a and B products. Therefore, it was confirmed that the dyeing property under alkaline conditions was significantly enhanced as compared with general products (comparative example 1 and example 5).

Additionally, in dyeing with the dyeing composition, after application to hair, it was left for 15 minutes under the conditions of 30 ℃ and 60% humidity, washed with water only for 1 minute and then completely dried, and all dyeing was performed under the same conditions. Further, the dyed hair was stored at about 25 ℃ and 55% humidity for 4 hours or more, and then the change in color was measured using a color difference meter. For reference, a is a composition (general hair dye) used alone, and B is a composition prepared to have the same dye content, composition as a when a first agent containing a dye and a second agent containing an alkaline agent are mixed.

2. Evaluation of Hair dyeing ability at each pH after mixing

In order to evaluate the hair-dyeing ability at each pH after mixing the first agent and the second agent, an experiment was performed, and the results are shown in fig. 2. The dyeing hair and the laboratory equipment used are as follows.

Hair for dyeing: BM-W-A of the company BEALAX, Japan

Color difference meter for color measurement: LabSacn XE from HunterLab

pH meter: 780 of metrohm company

The mixture was used to such an extent that the measurement site of the electrode of the pH meter was immersed (25 ℃ C. of the mixture to a site 3cm or more of the electrode).

As a result of the experiment, as evaluation of dyeing ability under each pH condition, it was confirmed that there was no significant difference in dyeing performance under the conditions of pH6 to pH8, which is the main pH of a general hair dye product using a basic dye and a direct dye, but significantly excellent dyeing performance was exhibited at a higher pH of 9 or more (fig. 2).

3. Evaluation of Hair dyeing force according to kind of alkaline agent

The compositions of examples 5, 9, 10 and 11 were evaluated for hair-dyeing ability according to the type of alkaline agent, and the results are shown in FIG. 3. The dyeing hair and the laboratory equipment used are as follows.

Hair for dyeing: BM-W-A of the company BEALAX, Japan

Color difference meter for color measurement: LabSacn XE from HunterLab

pH meter: 780 of metrohm company

The mixture was used to such an extent that the measurement site of the electrode of the pH meter was immersed (25 ℃ C. of the mixture to a site 3cm or more of the electrode).

As a result of the experiment, as a result of evaluating the dyeing ability according to the kind of the alkaline agent under the same pH condition, it was found that there was a difference in the dyeing performance of the products using the basic dye and the direct dye according to the kind of the alkaline agent even at the same pH. It can be found that Monoethanolamine (MEA) or Aminomethylpropanol (AMP) has relatively more excellent dyeing properties than sodium hydroxide (NaOH) and potassium hydroxide (KOH) as inorganic alkaline agents (examples 5, 9, 10, 11).

4. Color retention evaluation according to pH

For the compositions of comparative example 1 and example 5, evaluation of color retention according to pH was performed using the following hair for dyeing and a laboratory instrument, and the results thereof are shown in fig. 4.

Hair for dyeing: BM-W-A of the company BEALAX, Japan

Color difference meter for color measurement: LabSacn XE from HunterLab

pH meter: 780 of metrohm company

The mixture was used to such an extent that the measurement site of the electrode of the pH meter was immersed (25 ℃ C. of the mixture to a site 3cm or more of the electrode).

A is hair dyed using the composition of example 5 under alkaline conditions (pH11), and B is hair dyed using the composition of comparative example 1 under pH 6. By changing the color of the hair when these two types of hair are repeatedly washed under the conditions of washing with a general shampoo, it is found that the hair dyed under alkaline conditions is darker even after washing and is excellent in maintaining the dyeing effect (comparative example 1, example 5).

5. Color retention evaluation in repeated washing

The composition of example 5 was evaluated for color retention during repeated washing using the following hair dyes and a laboratory instrument, and the results are shown in fig. 5.

Hair for dyeing: BM-W-A of the company BEALAX, Japan

Color difference meter for color measurement: LabSacn XE from HunterLab

By changing the color of the hair when the hair dyed under alkaline conditions (pH11) was repeatedly washed 20 times under the conditions of washing with a general shampoo, it was found that the color was hardly changed after washing 5 times or more, and thus the hair had an excellent effect of maintaining the color after dyeing (example 5).

On the other hand, even if the composition of example 5 in which the MEA of fig. 3 and the control (control) of fig. 5 are the same is used, the reason why the value of dE (delta e) is different is that, since dE is a method of measuring a change in hair color using a colorimeter, which is a numerical value measuring and representing changes in lightness, green and red, blue and yellow, even if the same coloring agent is used, the measured value may be different depending on hair conditions, coloring conditions, and the like. That is, fig. 3 was stained with a sample in which the pH was precisely adjusted to 11 in order to measure the staining effect according to the kind of alkaline agent, while the control of fig. 5 was a commercialized sample in which the pH was between about 11 and 12, and thus it was evaluated that a difference in dE occurred. This dE difference between the MEA of FIG. 3 and the control of FIG. 5 can be said to be of similar magnitude under actual use conditions.

Also, even if the composition of example 5 having the same value once in fig. 4 and once in fig. 5 is used, the reason why the dE value is different is due to the difference in hair that is commonly used in dyeing and the difference in specific dyeing conditions (the number of rubs, the temperature of water in washing, etc.).

6. Evaluation of color maintenance according to repeated washing (after 10 shampoo washes) and pH

In order to evaluate the color retention according to the washing repetition and pH, the pH of the formulation in which the first agent and the second agent were mixed immediately before dyeing was adjusted according to each condition, and then the dyeing effect, i.e., the after-dyeing effect, and the evaluation of the color retention after 10 shampoo washes were performed, and the results thereof are shown in fig. 6.

Shampoo using the Charming Green Shower Shampoo (Charming Green Shower Shampoo) of the present applicant, the Shampoo condition was performed in such a manner that the Shampoo was applied to the hair bundle, rubbed and massaged for 1 minute, and then thoroughly washed with warm water (about 30 degrees).

As a result of the experiment, it was confirmed that when 10 shampoo washes were performed, the color retention was significantly improved from pH9 or higher (fig. 6).

7. Evaluation of Hair dyeing ability based on pH storage conditions of first dose

In order to evaluate the hair-dyeing ability according to the pH storage conditions of the first part, the contents of the first part of the dyeing preparation were adjusted to pH3, pH7 and pH10, stored in a thermostat at 50 ℃ for 30 days, and then mixed with the second part immediately before dyeing the hair to evaluate the dyeing effect, and the results are shown in fig. 7. The target color of the staining was brown. As a result of the experiment, it was clearly observed that even the same dye combinations had different dyeing properties depending on the pH storage conditions of the first dose (fig. 7).

Further, the formulations were evaluated for dyeing effect and conditioning effect by adjusting the pH of the first formulation containing the dye to 3 to 10, keeping the same in a thermostat at 50 ℃ for 30 days, and then mixing each formulation with the second formulation containing an alkaline agent or an alkaline reducing agent. Specifically, 10 hair professional panelists judged the dyeing property and the conditioning effect (degree of hair damage) after use according to the respective conditions, and shown in the following table 1 at 5-point scale, respectively.

[ Table 1]

	pH3	pH4	pH5	pH6	pH7	pH8	pH9	pH10
									Dyeing effect	2.1	3.2	3.9	4.7	4.6	4.5	3.9	2.8
Conditioning effects (Hair Damage)	4.1	3.9	4.2	4.3	4.1	3.2	3.1	2.9

The test results confirmed that the first preparation was stored at a pH of 4 to 9, more preferably 4 to 7.5, and that the effect of the hair conditioning and protecting components contained in the product over time was inferior as the pH increased.

8. Professional panelist testing

A total of 40 panelists used the hair dye compositions prepared according to the above example 5 and comparative example 1 in person and evaluated the degree of body feeling on items of white hair hiding power, color expression power, scalp irritation, dyeing durability and color loss at a 5-point full scale, and the results thereof are shown in the following table 2.

[ Table 2]

Distinguishing	Example 5	Comparative example 1
			Satisfactory degree of coverage of white hair	3.5	1.5
Color expression satisfaction	3.3	2.8
			Scalp irritation satisfaction	3.4	3.8
Degree of satisfaction of dyeing durability	3.1	2.0
			Degree of satisfaction of fading during life	3.1	2.9

The experimental results confirmed that example 5, which contained the alkaline wool dyeing agent and was separated into the first and second agents, exhibited significantly better wool dyeing power than comparative example 1, and high stability.