Color developing composition as well as use method and application thereof

By using polyglycerol fatty acid esters, polyol fatty acid esters, alkyl glycerol ethers and surfactant compositions, a layered structure is formed, and the problems of high density and inappropriate water agents of existing cosmetic color development materials are solved, and colorful color development effects and excellent moisturizing effects are achieved.

CN119564525APending Publication Date: 2025-03-07SHANGHAI BAITAI BIOTECHNOLOGY CO LTD
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Patent Information

Application Number
CN202411727327.9
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2024-11-28
Publication Date
2025-03-07

AI Technical Summary

Technical Problem

The materials used for color development in existing cosmetics have problems such as high density, unsuitable water agents, emulsions and essences, and the color development mechanism is mainly light reflection, poor color, and poor heat resistance and stability.

Method used

The color development effect is achieved by forming a layered structure (vesicles or liquid crystals) using compositions of polyglycerol fatty acid esters, polyol fatty acid esters or alkyl glycerol ethers, and anionic or cationic surfactants.

Benefits of technology

It has achieved colorful aurora color effect, excellent color stability and excellent moisturizing effect, and is suitable for cosmetics, mouthwash, food and beverages and other products.

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Abstract

The invention discloses a color developing composition as well as a use method and application thereof. The color developing composition comprises the following components: a) polyglycerol fatty acid ester; b) at least one of polyol fatty acid ester and alkyl glyceryl ether; and c) at least one of an anionic surfactant and a cationic surfactant. According to the invention, through compounding of specific types of surfactants, the obtained color developing composition can present a color developing appearance after being diluted with water, has good color developing stability, and also has a polarization phenomenon and an excellent moisturizing effect; as a novel developing additive, the developing composition can be widely applied to products such as cosmetics, mouthwash, food and beverages, so that the products are colorful, and the safety is high.
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Description

Technical Field

[0001] The present invention belongs to the technical field of cosmetics, and specifically relates to a color developing composition and a method for using and application thereof, and in particular to a preparation of a layered structure (vesicle or liquid crystal) with a color developing effect prepared by using a surfactant and its application. Background Art

[0002] At present, there are a wide variety of cosmetics on the market. Each product highlights its appeal in its own unique way to stimulate consumers' desire to buy. In order to increase product sales, brands focus on the design of color and texture in containers and packaging. In terms of contents, most of them are currently working on the makeup formula, enhancing the appearance of the formula through a combination of three-dimensional molding and high-brightness pearlescent agents, and conveying the message to consumers that "you will become beautiful after using it." However, in the field of skin care, there is a relative lack of cases in the study of the appearance of preparations. Basically, mica, cholesteric liquid crystals, and high-carbon alcohol crystals are used to make pearlescent materials or pigments (natural or synthetic) to attract consumers. However, these solutions also have some flaws: mica has bright pearl luster but high density. Mica tends to sink to the bottom when stored for a long time, making it unsuitable for aqueous solutions, emulsions and essences, and the color development mechanism is mainly light reflection; the pearlescent color development mechanism formed by cholesteric liquid crystals and high-carbon alcohol crystals is mainly light reflection, but due to changes in temperature conditions and long-term storage, the liquid crystal and crystal state will change, the color will disappear or there will be problems with the stability of the formula, and the pearlescent color is only white or silver, and the color is not rich; the color development mechanism of pigments is the complementary color of natural visible light, but pigments (natural) are sensitive to ultraviolet rays, have poor heat stability, and are prone to color attenuation or discoloration; pigments (synthetic) do not conform to current environmental protection and green trends. Summary of the invention

[0003] In view of the deficiencies in the prior art, the object of the present invention is to provide a color developing composition and a method for using and application thereof.

[0004] The objective of the present invention is achieved through the following technical solutions:

[0005] In a first aspect, the present invention provides a color developing composition comprising the following components:

[0006] a) polyglycerol fatty acid esters;

[0007] b) at least one of polyol fatty acid esters and alkyl glyceryl ethers;

[0008] c) at least one of anionic surfactants and cationic surfactants.

[0009] As a preferred embodiment, the glycerol group of the polyglycerol fatty acid ester has any polymerization degree, and the carbon number of the fatty acid is 8 to 18, more preferably 12 to 18, and most preferably 12. The carbon chain of the fatty acid can be a straight chain saturated structure or an unsaturated structure. When the carbon number of the fatty acid is less than 12, the color development composition is severely turbid and almost no color development is seen.

[0010] As a preferred embodiment, the polyglycerol fatty acid ester has a glycerol polymerization degree of 2. When the glycerol polymerization degree is 3 or more, the color-developing composition is severely turbid, and color development is almost invisible or there is stratification.

[0011] As a preferred embodiment, part or all of the polyglycerol fatty acid is esterified; more preferably, only one hydroxyl group is esterified, which can further improve the color stability.

[0012] As a preferred embodiment, the carbon number of the fatty acid in the polyol fatty acid ester or alkyl glyceryl ether is 8 to 18, more preferably 12 to 18, and most preferably 12. When the carbon number of the fatty acid (alcohol) is less than 12, the color developing composition is severely turbid and color development is almost invisible.

[0013] As a preferred embodiment, the hydrophilic group of the polyol fatty acid ester or alkyl glyceryl ether has 2 to 6 carbon atoms, more preferably 3. When the hydrophilic group has more than 3 carbon atoms, the color developing composition becomes severely turbid and color development is hardly visible.

[0014] As a preferred embodiment, part or all of the polyol fatty acid ester or alkyl glyceryl ether is esterified or etherified; more preferably, only one hydroxyl group is esterified or etherified, which can further improve the color stability.

[0015] As a preferred embodiment, the anionic surfactant is at least one of a single-chain anionic surfactant and a Gemini anionic surfactant.

[0016] As a preferred embodiment, the single-chain anionic surfactant includes at least one of sodium methyl cocoyl taurate and fatty acid salt.

[0017] As a preferred embodiment, the Gemini anionic surfactant refers to an anionic surfactant having at least two hydrophobic hydrocarbon chains, two hydrophilic head groups and one connecting group, including at least one of sodium di(laurylamide glutamine) lysine and sodium di(laureth-10) phosphate.

[0018] As a preferred embodiment, the cationic surfactant includes distearyl dimethyl ammonium chloride.

[0019] As a preferred embodiment, the color developing composition comprises the following components:

[0020] a) polyglycerol fatty acid ester; the degree of polymerization of the glycerol group of the polyglycerol fatty acid ester is 2, the number of carbon atoms of the fatty acid is 12 to 18, and only one of the hydroxyl groups in the polyglycerol fatty acid ester is esterified;

[0021] For example, at least one of polyglyceryl-2 laurate, polyglyceryl-2 myristic acid ester, polyglyceryl-2 palmitate, polyglyceryl-2 isostearate, polyglyceryl-2 oleate, etc. may be selected;

[0022] b) at least one of a polyol fatty acid ester and an alkyl glyceryl ether; wherein the polyol fatty acid ester or the alkyl glyceryl ether has 12 to 18 carbon atoms in the fatty acid, 3 carbon atoms in the hydrophilic group, and only one of the hydroxyl groups is esterified or etherified;

[0023] For example, at least one of lauryl glyceryl ether, myristyl glyceryl ether, palmityl glyceryl ether, isostearyl glyceryl ether, oleyl glyceryl ether, propylene glycol laurate, propylene glycol myristate, propylene glycol palmitate, propylene glycol isostearate, propylene glycol oleate, glyceryl laurate, glyceryl oleate, glyceryl isostearate, etc. can be selected;

[0024] c) anionic surfactant or cationic surfactant; for example, at least one selected from sodium methyl cocoyl taurate, di(lauryl glutamine) lysine, sodium di(laureth-10) phosphate, potassium laurate, potassium myristate, potassium palmitate, distearyl dimethyl ammonium chloride, etc.

[0025] As a preferred embodiment, the overall HLB value of the components a) and b) is in the range of 7.0 to 8.5. More preferably, the overall HLB value of the components a) and b) is in the range of 7.26 to 7.87.

[0026] As a preferred embodiment, the total mass of the components a) and b) is 57 to 2125 times the mass of the component c).

[0027] As a preferred embodiment, other components are also included; the other components are selected from polyols (such as glycerol, propylene glycol, 1,3-propanediol, butylene glycol, pentylene glycol, isopentyl glycol, hexylene glycol, polyethylene glycol, caprylyl glycol, sorbitol, dipropylene glycol, etc.), chelating agents (such as disodium EDTA, trisodium EDTA, tetrasodium EDTA, dipotassium EDTA, tripotassium EDTA, etc.), oils (such as macadamia ternifolia seed oil, avocado oil, corn germ oil, jojoba oil, etc.), CHINENSIS) seed oil, squalane, mineral oil, phenyl trimethicone, isopropyl myristate, triethylhexanoin, phytosteryl / octyldodecanol lauroyl glutamate, ceramide NP, etc.), fatty alcohols (such as fatty alcohols: oleyl alcohol, cetyl alcohol, etc.), fatty acids (such as oleic acid, stearic acid, etc.), flavors, preservatives (such as phenoxyethanol, methylparaben, ethylparaben, etc.), amino acids (such as glycine, taurine, sarcosine, glutamic acid, arginine, citrulline, theanine, serine, cysteine, etc.), vitamins and their derivatives (such as panthenol, tocopherol (vitamin E), tocopheryl acetate, niacinamide, retinol, retinyl palmitate, ascorbyl palmitate, etc.), amphiphilic substances (such as PEG / PPG / polybutylene glycol-8 / 5 / 3 glycerol, PPG-7-butanol polyether-10, etc.), and at least one of water. As long as the other components do not affect the color development of the composition, there is no particular limitation on their specific types and addition amounts.

[0028] As a further preferred embodiment, when the other components added are polyols, the most preferred polyol is 1,3-propylene glycol, and its addition amount can be up to 36 times the total amount of the color-developing composition (i.e., component a), component b) and component c); followed by butanediol, and its addition amount can be up to 12 times the total amount of the color-developing composition; under the aforementioned addition amount, the color development effect of the color-developing composition will not be adversely affected. If the polyol used is glycerol, sorbitol, dipropylene glycol, 1,2-hexanediol, etc., its addition amount must be less than 5 times the total amount of the color-developing composition, otherwise it will affect the color development effect.

[0029] As a further preferred embodiment, the color developing composition comprises the following components:

[0030] a) polyglycerol fatty acid esters;

[0031] b) at least one of polyol fatty acid esters and alkyl glyceryl ethers;

[0032] c) at least one of anionic surfactants and cationic surfactants;

[0033] d) Water.

[0034] As a further preferred embodiment, based on the total mass of 100% of the color developing composition, the total mass of component a) and component b) is 87-98.0%, the mass of component c) is 0.04-1.72%, and component d) is the balance.

[0035] As a further preferred embodiment, the total mass of component a) and component b) in the color developing composition is 94.7-97.5%, most preferably 95.6-97.5%.

[0036] In a second aspect, the present invention provides a method for color development according to the aforementioned color development composition, comprising the following steps: adding the color development composition to water for dilution;

[0037] Wherein, when water is used for dilution, the dilution multiple of water is 25 to 200 times the total mass of components a), b) and c) in the color developing composition.

[0038] As a preferred embodiment, the dilution ratio of water is 50 to 67 times the total mass of components a), b) and c) in the color developing composition.

[0039] In a third aspect, the present invention provides a use of the aforementioned color-developing composition in the preparation of color-developing cosmetics, mouthwashes, or food and beverages.

[0040] Compared with the prior art, the present invention has the following beneficial effects:

[0041] 1) The present invention develops an optical principle produced by a layered structure (lamellar liquid crystal or vesicle) produced solely by the compounding of surfactants, so that the formulated color-developing composition has a color appearance including colorful aurora colors (aurora color definition: a single color or a combination of multiple colors); the color seen by the front reflected light and the color seen by the back transmitted light are two different colors of light in a complementary color relationship; when the observation angle deviates from the incident light angle, it can be seen that the color will also change and different colors will be observed; some preparations have fire color or rainbow luster under a polarizing plate, and the color stability is excellent over time, thereby providing the expected effects that these traditional appearances cannot achieve, and have excellent moisturizing effects.

[0042] 2) The present invention can further improve the color development effect and color development stability by further optimizing the type selection of each component in the color development composition, the overall HLB value range of the non-ionic surfactant used, and the mass ratio of the non-ionic surfactant used to the ionic surfactant used.

[0043] 3) The color-developing composition prepared by the present invention can be widely used as a new color-developing additive in cosmetics, mouthwashes, food and beverages and other products, making the products present colorful colors and having high safety. BRIEF DESCRIPTION OF THE DRAWINGS

[0044] Other features, objects and advantages of the present invention will become more apparent from the detailed description of non-limiting embodiments made with reference to the following drawings:

[0045] Figure 1 These are the color photos of experimental groups 1-1, 1-2, 1-3, and 1-4;

[0046] Figure 2 These are the chromogenic photographs of experimental groups 1-5, 1-6, 1-7, 1-8, and 1-9;

[0047] Figure 3 These are the color photos of experimental groups 1-10 and 1-11;

[0048] Figure 4 The color development photos of the color development compositions of Examples 1-5 and Comparative Examples 1-2;

[0049] Figure 5 The color development photos of the color development compositions of Examples 6-11 and Comparative Examples 3-4;

[0050] Figure 6 The color development photos of the color development compositions of Examples 12-19 and Comparative Example 5;

[0051] Figure 7 The color development photos of the color development compositions of Examples 2 and 20 and Comparative Examples 6-10;

[0052] Figure 8 The color development photos of the color development compositions of Examples 2 and 21 and Comparative Examples 11-14;

[0053] Fig. 9 The color development photos of the color development compositions of Examples 22-26 and Comparative Examples 15-16;

[0054] Fig.10 This is a diagram of the color rendering mechanism of visible light colors;

[0055] Fig.11 The color development photos of the color development composition of Example 27 at different addition ratios are shown; wherein, Fig.11 A is a darkroom photo (front view); Fig.11 B is a darkroom photo (vertical); Fig.11 C is a photo taken in a dark room with the light source facing the front (side view); Fig.11 D is a photo taken in a dark room with the light source at the back (front view); Fig.11 E is a photo taken with polarized light in a dark room (front view); Fig.11 F is a photo taken in a dark room with the light source at the bottom (vertical). DETAILED DESCRIPTION

[0056] The present invention is described in detail below in conjunction with specific embodiments. The following embodiments will help those skilled in the art to further understand the present invention, but are not intended to limit the present invention in any form. It should be noted that, for those of ordinary skill in the art, several variations and improvements may be made without departing from the concept of the present invention. These all belong to the protection scope of the present invention.

[0057] The words "preferred", "preferably", "more preferably", etc. in the present invention refer to embodiments of the present invention that can provide certain beneficial effects in certain circumstances. However, other embodiments may also be preferred under the same circumstances or other circumstances. In addition, the description of one or more preferred embodiments does not imply that other embodiments are not applicable, nor is it intended to exclude other embodiments from the scope of the present invention.

[0058] It should be understood that, except in any operating examples, or otherwise indicated, all numbers representing the amount of ingredients used in the specification and claims should be understood to be modified by the term "about" in all cases. Therefore, unless otherwise indicated, the numerical parameters set forth in the following specification and the appended claims are approximate values ​​that vary according to the desired performance to be obtained by the present invention. At least, it is not intended to limit the application of the doctrine of equivalents to the scope of the claims, and each numerical parameter should at least be interpreted according to the number of reported significant figures and by applying ordinary rounding techniques.

[0059] Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values ​​set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements.

[0060] In the specific embodiment of the present invention, all raw materials, reagents, etc. used are commercially available products. For example, polyglyceryl-2 laurate comes from POEM DL-100 of Riken; polyglyceryl-2 oleate comes from POEM DO-100V of Riken; propylene glycol laurate comes from BIOTHICKNER TYPE BP of Riken; lauryl glyceryl ether comes from 1-O-Dodecylglycerol of MedChemExpress; alkyl glyceryl ether comes from NIKKOL Selachyl Alcohol V of Nikkol; sodium methyl cocoyl taurate comes from DIAPON of TOHO TMK-SF, with an active content of 30%; sodium di(lauryl glutamine) lysine comes from Pellicer L-30 of Asahikasei, with an active content of 29%; sodium di(laureth-10) phosphate comes from NIKKOL DLP-10 of NIKKOL, with an active content of 100%; potassium laurate, potassium myristate, and potassium palmitate come from PRIOLY B-100 of Kao, with an active content of 32.5%; distearyl dimethyl ammonium chloride comes from Varisoft TA100 of Evonik, with an active content of 100%; cocamidopropyl betaine comes from TC-CAB 35H of Tianci, with an active content of 31%; hydrogenated lecithin comes from Lipoid's 80H, effective content is 100%; 1,3-propylene glycol comes from Dupont Propanediol; Polyglyceryl-2 caprate from Taiyo Kagaku's SUNSOFT Q-10D; Polyglyceryl-2 diisostearate from Nisshin oil's COSMOL 42V; Lauryl glyceryl ether from MedChemExpress's 1-O-Dodecylglycerol; Polyglyceryl-3 laurate from NIKKOL Triglyn 1-L from NIKKOL; Polyglyceryl-4 laurate from Sakamoto's SY-Glyster ML-310; Polyglyceryl-5 laurate from Taiyo Kagaku's SUNSOFT A-12E-C; Propylene glycol caprylate from NIKKOL's NIKKOL Sefsol-218; Propylene glycol isostearate from Croda's CITHROL PGMIS; Butylene glycol laurate from NOF's Comupoal BL; Propylene glycol dicaprate from NIKKOL's NIKKOL PDD; Oleyl glyceryl ether from NIKKOL's NIKKOL Selachyl Alcohol V.

[0061] In a specific embodiment of the present invention, the specific method for performing performance testing is as follows:

[0062] 1) Evaluation of color development effect and color development stability

[0063] The instant color development of each color developing composition was visually evaluated in a dark room or under indoor light according to the following criteria. The color developing composition was also observed for stability under specific conditions (color development stability criteria), then returned to room temperature and subjected to the same visual evaluation to evaluate the color development stability.

[0064] - Instant color rendering criteria -

[0065] Acceptable (Excellent) ◎: No turbidity is observed at all, the color is good, and there is an aurora color.

[0066] Acceptable (good) ○: Some turbidity is observed, but the color development is good; or, no turbidity is observed at all, but the color development is weak.

[0067] Unqualified (slightly poor) △: Some white turbidity and weak color development.

[0068] Unqualified (very poor) ×: Severe turbidity, almost no color development; or some turbidity, no color development.

[0069] - Criteria for determining color stability -

[0070] Pass (Excellent)◎: Cycle test (-10~40℃: stored at -10℃ for 24h; stored at 25℃ for 24h; stored at 40℃ for 24h; stored at 25℃ for 24h and 4 days as a cycle), no obvious change in color for 1 month.

[0071] Acceptable (good) ○: No significant change in color after 24 hours at room temperature.

[0072] Unqualified ×: The color disappears or is significantly weakened within 24 hours at room temperature.

[0073] 2) Criteria for determining the formation of layered structures

[0074] Observe whether there is a layered liquid crystal texture through the polarizing plate

[0075] ○: There is polarization phenomenon

[0076] ×: No polarization

[0077] 3) Measurement of skin moisture content and evaluation of moisture retention function

[0078] The moisture content of the stratum corneum of the skin was tested using the Corneometer CM825 (Courage-Khazaka) instrument for 4 hours. The test method was QB / T 4256-2011. The percentage increase in the moisture content of the stratum corneum of the skin was calculated. The higher the value, the higher the moisture retention capacity.

[0079] Moisturizing efficacy criteria

[0080] ○: After 4 hours, the increase rate of moisture content in the stratum corneum of the skin is ≥10%

[0081] ×: After 4 hours, the increase rate of moisture content in the stratum corneum of the skin is <10%

[0082] In the preliminary research of the present invention, according to the reports in the existing literature, the critical packing parameter (CPP) has a close relationship with the aggregates. When CPP < 1 / 3, it is a spherical micelle; when 1 / 3 < CPP < 1 / 2, it is a rod-shaped micelle; when 1 / 2 < CPP < 1, it is a vesicle; when CPP ≈ 1, it is a flat sheet; and when CPP > 1, an inverse micelle is formed. Therefore, vesicles can be formed by using amphiphiles with 1 / 2 < CPP < 1 or mixing an appropriate amount of various amphiphiles to form an amphiphile mixture system with 1 / 2 < CPP < 1. So, the present invention selects a combination of surfactants with an overall HLB value in the range of 5 - 10 to attempt to develop a color-developing preparation.

[0083] The state of surfactants dissolved in water generally varies with changes in temperature and concentration, accompanied by various changes in the aggregate morphology, such as single-molecule dispersions, micellar solutions, or liquid crystal formation. Many existing surfactants do not show spherical micelles at low concentrations and can be classified as water-insoluble surfactants. The dissolution behavior of water-insoluble surfactants is different from that of ordinary surfactants, and its uniqueness lies in that it is easy to form liquid crystals even at low concentrations. Many so-called double-chain ionic surfactants in the dissolved state, such as lecithin and dialkyldimethylammonium chloride, have been reported to exhibit this unique dissolved state. Based on this theory, the present invention focuses on water-insoluble surfactants with an overall HLB value in the range of 5 - 10, among which surfactants with a single highly linear alkyl group and a hydrophilic structure of hydroxyl have this property.

[0084] Based on this, in the preliminary experiments of the present invention, surfactants were screened. A single non-ionic surfactant with an HLB value in the range of 5 - 10 was added to water to observe color development. The formulations (mass percentages) of each experimental group are shown in Table 1 below, and the color development results are shown in Table 1 and Figure 1 as shown. From the results in Table 1 and Figure 1 it can be seen that the immediate color development evaluations of experimental groups 1-1, 1-2, 1-3, and 1-4 are all unqualified (very poor). Therefore, a single non-ionic surfactant cannot develop color.

[0085] Table 1

[0086]

[0087] The present invention further compounded two non-ionic surfactants and controlled the overall HLB value to be in the range of 7.0 - 8.0, and then added them to water to observe color development. The formulations (mass percentages) of each experimental group are shown in Table 2 below, and the color development results are shown in Table 2 and Figure 2 ( Figure 2 in which, the upper figure is the front view and the lower figure is the vertical view) as shown. From Table 2 and Figure 2The results show that the instant color development evaluation of experimental groups 1-5, 1-6, 1-7, 1-8, and 1-9 is unqualified (very poor), so when non-ionic surfactants are compounded in pairs and the overall HLB value is controlled under the conditions that meet the formation of vesicles, color development is still not possible.

[0088] Table 2

[0089]

[0090]

[0091] The present invention further adds a single nonionic surfactant and a single anionic surfactant to water for color development. The formula (mass percentage) of each experimental group is shown in Table 3 below. The color development results are shown in Table 3 and Figure 3 As shown in Table 3 and Figure 3 The results show that the instant color development evaluation of experimental groups 1-10 and 1-11 is unqualified (very poor), so the use of a single nonionic surfactant and a single anionic surfactant in combination also fails to develop color.

[0092] Table 3

[0093]

[0094] Based on the above experimental studies, the present invention further optimizes the selection of surfactants, thereby obtaining the color developing composition of the present invention. The following examples will describe the color developing composition of the present invention in detail.

[0095] Examples 1-5

[0096] Embodiments 1-5 provide a color development composition, which includes a nonionic surfactant (a) polyglycerol-2 laurate and b) propylene glycol laurate), and also includes c) an anionic surfactant or a cationic surfactant. The specific raw materials used in the color development composition of Embodiments 1-5 are shown in Table 4. Each color development composition prepared in Embodiments 1-5 is added to water according to the mass percentage shown in Table 4, and the color development is observed. The specific method is:

[0097] S1: Weigh the raw materials of the color developing composition and water according to the ratio shown in Table 4;

[0098] S2: Put all the ingredients into the main pot, heat to above 75°C while stirring, and continue stirring for 10 minutes at a stirring speed of 450 rpm;

[0099] S3: Cool in a water bath to below 35°C, stirring at 450 rpm throughout the process.

[0100] The solution after the color-developing composition was mixed with water was evaluated. The results of the immediate color development evaluation, color development stability evaluation, and layer structure formation state evaluation are shown in Table 4 and Figure 4 ( Figure 4 , the upper figure is a front view and the lower figure is a vertical view).

[0101] Comparative Example 1-2

[0102] Comparative Example 1-2 provides a color development composition, which includes a nonionic surfactant (a) polyglycerol-2 laurate and b) propylene glycol laurate), and also includes c) a zwitterionic surfactant. The specific raw materials used in the color development composition of Comparative Example 1-2 are shown in Table 4. Each color development composition prepared in Comparative Example 1-2 is added to water according to the mass percentage shown in Table 4, and the color development is observed in the same manner as in Example 1-5.

[0103] The solution after the color-developing composition was mixed with water was evaluated. The results of the immediate color development evaluation, color development stability evaluation, and layer structure formation state evaluation are shown in Table 4 and Figure 4 ( Figure 4 , the upper figure is a front view and the lower figure is a vertical view).

[0104] Table 4

[0105]

[0106] From Table 4 and Figure 4 It can be seen from the results that the ionic surfactants used in Implementation Columns 1-4 are anionic surfactants, and the instant color development evaluation is qualified (excellent), and the layered structure formation state evaluation has polarization phenomenon. Among them, Examples 1 and 4 use a monoalkyl chain anionic surfactant, and its color development stability evaluation is qualified (good), while Examples 2 and 3 use Gemini anionic surfactants, and its color development stability evaluation is qualified (excellent). The ionic surfactant used in Implementation Column 5 is a cationic surfactant, and the result is that the instant color development evaluation is qualified (excellent), the color development stability evaluation is qualified (good), and the layered structure formation state evaluation has polarization phenomenon. The ionic surfactant used in Comparative Columns 1-2 is an amphoteric surfactant, and its instant color development evaluation is unqualified (very poor), and the layered structure formation state evaluation has no polarization phenomenon.

[0107] The results of Example 1-5 and Comparative Column 1-2 show that both anionic surfactants and cationic surfactants in ionic surfactants are helpful for color development, and Gemini anionic surfactants are more helpful for color development stability. The reason may be that single-chain anionic surfactants such as sodium methyl cocoyl taurate and fatty acid salts will separate from the layered structure due to their own structural reasons and form spherical micelles by themselves, while Gemini ionic surfactants are not easy to separate from the layered structure.

[0108] Embodiment 6-11

[0109] Embodiment 6-11 provides a color development composition, which includes a nonionic surfactant (a) polyglycerol-2 laurate and b) propylene glycol laurate), and also includes c) an anionic surfactant. The specific raw materials used in the color development composition of Embodiment 6-11 are shown in Table 5. Each color development composition prepared in Embodiment 6-11 is added to water according to the mass percentage shown in Table 5, and the color development is observed in the same manner as in Embodiment 1-5.

[0110] The solution after the color-developing composition was mixed with water was evaluated. The results of the immediate color development evaluation, color development stability evaluation, and layer structure formation state evaluation are shown in Table 5 and Figure 5 ( Figure 5 , the upper figure is a front view and the lower figure is a vertical view).

[0111] Comparative Examples 3-4

[0112] Comparative Examples 3-4 provide a color development composition, which includes a nonionic surfactant (a) polyglycerol-2 laurate and b) propylene glycol laurate), and also includes c) an anionic surfactant. The specific raw materials used in the color development composition of Comparative Examples 3-4 are shown in Table 5. Each color development composition prepared in Comparative Examples 3-4 is added to water according to the mass percentage shown in Table 5, and the color development is observed in the same manner as in Examples 1-5.

[0113] The solution after the color-developing composition was mixed with water was evaluated. The results of the immediate color development evaluation, color development stability evaluation, and layer structure formation state evaluation are shown in Table 5 and Figure 5 ( Figure 5 , the upper figure is a front view and the lower figure is a vertical view).

[0114] Table 5

[0115]

[0116]

[0117] From Table 5 and Figure 5The results show that the overall HLB value of the nonionic surfactants used in Examples 6-11 is between 7.00 and 8.5, and the mass ratio of nonionic surfactants to ionic surfactants is between 147 and 586. The instant color development evaluation is qualified (good or excellent), the color stability evaluation is qualified (good or excellent), and the layered structure formation state evaluation has polarization phenomenon. Among them, the overall HLB value of the nonionic surfactants used in Examples 7-9 is between 7.26 and 7.87, and the mass ratio of nonionic surfactants to ionic surfactants is between 246 and 586, and the instant color development evaluation is qualified (excellent). In Examples 10-11 and Comparative Examples 3-4, when the mass ratio of nonionic surfactants to ionic surfactants is the same, when the overall HLB value of the nonionic surfactants used in Comparative Example 3 is less than 7, the instant color development evaluation is unqualified (very poor), and the layered structure formation state evaluation has no polarization phenomenon; when the overall HLB value of the nonionic surfactants used in Comparative Example 4 is greater than 8.5, the instant color development evaluation is unqualified (very poor), and the layered structure formation state evaluation has no polarization phenomenon.

[0118] The results of Example 6-11 and Comparative Columns 3-4 show that when the overall HLB value of the nonionic surfactant is 7.00-8.5, it is helpful for color development, and when the overall HLB value of the nonionic surfactant is 7.26-7.87, the color development effect is better.

[0119] Examples 12-19

[0120] Examples 12-19 provide a color development composition, which includes a nonionic surfactant (a) polyglycerol-2 laurate and b) propylene glycol laurate), and also includes c) an anionic surfactant. The specific raw materials used in the color development composition of Examples 12-19 are shown in Table 6. The color development compositions prepared in Examples 12-19 and the polyol (1,3-propylene glycol) are added to water according to the mass percentages shown in Table 6, and the color development is observed. The specific method is:

[0121] S1: weigh the raw materials of the color developing composition, 1,3-propylene glycol and water according to the proportions shown in Table 6;

[0122] S2: Put all the ingredients into the main pot, heat to above 75°C while stirring, and continue stirring for 10 minutes at a stirring speed of 450 rpm;

[0123] S3: Cool in a water bath to below 35°C, stirring at 450 rpm throughout the process.

[0124] The solution obtained by mixing the color developing composition, 1,3-propylene glycol and water was evaluated. The results of the immediate color development evaluation, the color development stability evaluation and the layer structure formation state evaluation are shown in Table 6 and Figure 6 ( Figure 6, the upper figure is a front view and the lower figure is a vertical view).

[0125] Comparative Example 5

[0126] Comparative Example 5 provides a color development composition, which includes a nonionic surfactant (a) polyglycerol-2 laurate and b) propylene glycol laurate), and also includes c) an anionic surfactant. The specific raw materials used in the color development composition of Comparative Example 5 are shown in Table 6. Each color development composition prepared in Comparative Example 5 and a polyol (1,3-propylene glycol) are added to water according to the mass percentage shown in Table 6, and the color development is observed in the same manner as in Examples 12-19.

[0127] The solution obtained by mixing the color developing composition, 1,3-propylene glycol and water was evaluated. The results of the immediate color development evaluation, the color development stability evaluation and the layer structure formation state evaluation are shown in Table 6 and Figure 6 ( Figure 6 , the upper figure is a front view and the lower figure is a vertical view).

[0128] Table 6

[0129]

[0130] From Table 6 and Figure 6 The results show that, when the overall HLB value of the nonionic surfactant used in Examples 12-19 is consistent, the mass ratio of the nonionic surfactant to the ionic surfactant used is 57-2125, the instant color development evaluation is qualified (good or excellent), the color stability evaluation is qualified (excellent), and the layered structure formation state evaluation has polarization phenomenon. Compared with Comparative Example 5, the mass ratio of the nonionic surfactant to the ionic surfactant used in Comparative Example 5 is 47, the instant color development evaluation is unqualified (slightly worse), and the layered structure formation state evaluation has polarization phenomenon.

[0131] The results of Example 18-19 and Comparative Column 5 show that when the anionic surfactant used is sodium di(laureth-10) phosphate, the mass ratio of the nonionic surfactant to the ionic surfactant is 57 to 2125, which is conducive to color development. The results of Examples 12-17 show that when the anionic surfactant used is sodium di(laurylamide glutamine) lysine, the mass ratio of the nonionic surfactant to the ionic surfactant is 404 to 803, which is conducive to color development.

[0132] Embodiment 20

[0133] Example 20 provides a color development composition, which includes a nonionic surfactant (a) polyglycerol-2 oleate and b) propylene glycol laurate), and also includes c) an anionic surfactant. The specific raw materials used in the color development composition of Example 20 are shown in Table 7. The color development composition prepared in Example 20 is added to water according to the mass percentage shown in Table 7, and the color development is observed in the same manner as in Examples 1-5.

[0134] The solution after the color-developing composition was mixed with water was evaluated. The results of the immediate color development evaluation, color development stability evaluation, and layer structure formation state evaluation are shown in Tables 7 and Figure 7 ( Figure 7 , the upper figure is a front view and the lower figure is a vertical view).

[0135] Comparative Examples 6-10

[0136] Comparative Examples 6-10 provide a color development composition, which includes a nonionic surfactant (a) one or two of polyglycerol-2 laurate, glycerol-2 oleate, glycerol-2 caprate, glycerol-3 laurate, glycerol-4 laurate, and glycerol-5 laurate; and b) propylene glycol laurate or lauryl glyceryl ether), and also includes c) anionic surfactant. The specific raw materials used in the color development composition of Comparative Examples 6-10 are shown in Table 7. Each color development composition prepared in Comparative Examples 6-10 is added to water according to the mass percentage shown in Table 7, and the color development is observed. The method is the same as that of Examples 1-5.

[0137] The solution after the color-developing composition was mixed with water was evaluated. The results of the immediate color development evaluation, color development stability evaluation, and layer structure formation state evaluation are shown in Tables 7 and Figure 7 ( Figure 7 , the upper figure is a front view and the lower figure is a vertical view).

[0138] Table 7

[0139]

[0140]

[0141] From Table 7 and Figure 7The results show that, compared with Example 6, when the overall HLB value of the nonionic surfactant used is consistent and the mass ratio of the nonionic surfactant to the ionic surfactant is consistent, when the polyglycerol fatty acid ester used is polyglycerol-2 oleate, the instant color development evaluation is qualified (excellent), the color stability evaluation is qualified (excellent), and the layered structure formation state evaluation has polarization phenomenon; when the polyglycerol fatty acid ester used is polyglycerol-2 caprate (the number of carbon atoms in the fatty acid group is less than 12), the instant color development evaluation is unqualified (slightly worse), and the layered structure formation state evaluation has no polarization phenomenon. Compared with Example 2, when the overall HLB value of the nonionic surfactant used is basically consistent and the mass ratio of the nonionic surfactant to the ionic surfactant is consistent, after adding polyglycerol-2 diisostearate, the instant color development evaluation is unqualified (slightly worse), and the layered structure formation state evaluation has polarization phenomenon. Compared with Example 2, in Comparative Examples 8-10, when the overall HLB value of the non-ionic surfactant used is basically the same and the mass ratio of the non-ionic surfactant to the ionic surfactant is the same, polyglyceryl-3 laurate, polyglyceryl-4 laurate or polyglyceryl-5 laurate is added, the immediate color development evaluation is unqualified (very poor or slightly poor), and there is no polarization phenomenon in the evaluation of the layered structure formation state.

[0142] The results of Example 2 and 20 and Comparative Columns 6-10 show that when the carbon number of the fatty acid group in the polyglycerol fatty acid ester used is 12 to 18, it is helpful to color development; when only one hydroxyl group in the polyglycerol fatty acid ester used is esterified (polyglycerol monofatty acid ester), it is helpful to color development; when the degree of glycerol polymerization of the polyglycerol fatty acid ester is 2, it is helpful to color development.

[0143] Embodiment 21

[0144] Example 21 provides a color developing composition, which includes a nonionic surfactant (1) polyglycerol-2 laurate; and 2) oleyl glyceryl ether), and also includes c) an anionic surfactant. The specific raw materials used in the color developing composition of Example 20 are shown in Table 7. The color developing composition prepared in Example 21 is added to water according to the mass percentage shown in Table 8, and the color development is observed in the same manner as in Examples 12-19.

[0145] The solution obtained by mixing the color developing composition, 1,3-propylene glycol and water was evaluated. The results of the immediate color development evaluation, the color development stability evaluation and the layer structure formation state evaluation are shown in Table 8 and Figure 8 ( Figure 8 , the upper figure is a front view and the lower figure is a vertical view).

[0146] Comparative Examples 11-14

[0147] Comparative Examples 11-14 provide a color development composition, which includes a nonionic surfactant (a) polyglycerol-2 laurate; and b) one or two of propylene glycol laurate, propylene glycol caprylate, propylene glycol isostearate, butylene glycol laurate, and propylene glycol dicaprate), and c) an anionic surfactant. The specific raw materials used in the color development composition of Comparative Examples 11-14 are shown in Table 8. Each color development composition prepared in Comparative Examples 11-14 was added to water according to the mass percentage shown in Table 8, and the color development was observed in the same manner as in Examples 12-19.

[0148] The solution obtained by mixing the color developing composition, 1,3-propylene glycol and water was evaluated. The results of the immediate color development evaluation, the color development stability evaluation and the layer structure formation state evaluation are shown in Table 8 and Figure 8 ( Figure 8 , the upper figure is a front view and the lower figure is a vertical view).

[0149] Table 8

[0150]

[0151] From Table 8 and Figure 8 The results show that Example 21 uses nonionic surfactants such as polyglycerol-2 laurate and oleyl glyceryl ether, and the instant color development evaluation is qualified (excellent), the color development stability evaluation is qualified (excellent), and the layered structure formation state evaluation has polarization phenomenon. Comparative Examples 11-13 Compared with Example 2, the overall HLB value of the nonionic surfactant used is consistent, and the mass ratio of the nonionic surfactant to the ionic surfactant is consistent. The polyol fatty acid esters used are propylene glycol caprylate, propylene glycol isostearate or butylene glycol laurate. The instant color development evaluation is unqualified (very poor), and the layered structure formation state evaluation has no polarization phenomenon. Comparative Example 14 Compared with Example 2, the overall HLB value of the nonionic surfactant used is basically the same, and the mass ratio of the nonionic surfactant to the ionic surfactant is close. After propylene glycol dicaprate is added, the instant color development evaluation is unqualified (very poor), and the layered structure formation state evaluation has no polarization phenomenon.

[0152] The results of Example 2 and Comparative Examples 11-14 show that when the number of carbon atoms in the fatty acid in the polyol fatty acid ester used is 12 to 18 (such as lauric acid), it is helpful to color development; when the number of carbon atoms in the hydrophilic group in the polyol fatty acid ester used is equal to 3 (such as propylene glycol), it is helpful to color development; when only one hydroxyl group in the polyol fatty acid ester or alkyl glyceryl ether used is esterified (polyol monofatty acid ester / alkyl glyceryl monoether), it is helpful to color development.

[0153] Examples 22-26

[0154] Examples 22-26 provide a color development composition, which includes a nonionic surfactant (a) polyglycerol-2 laurate and b) propylene glycol laurate), and also includes c) an anionic surfactant. The specific raw materials used in the color development composition of Examples 22-26 are shown in Table 9. The color development compositions prepared in Examples 22-26 and the polyol (1,3-propylene glycol) are added to water according to the mass percentages shown in Table 9, and the color development is observed in the same manner as in Examples 12-19.

[0155] The solution obtained by mixing the color developing composition, 1,3-propylene glycol and water was evaluated. The results of the immediate color development evaluation, the color development stability evaluation and the layer structure formation state evaluation are shown in Tables 9 and Fig. 9 ( Fig. 9 , the upper figure is a front view and the lower figure is a vertical view).

[0156] Comparative Examples 15-16

[0157] Comparative Examples 15-16 provide a color development composition, which includes a nonionic surfactant (a) polyglycerol-2 laurate and b) propylene glycol laurate), and also includes c) an anionic surfactant. The specific raw materials used in the color development composition of Comparative Examples 15-16 are shown in Table 9. The color development compositions prepared in Comparative Examples 15-16 and polyols (1,3-propylene glycol) are added to water according to the mass percentages shown in Table 9, and the color development is observed in the same manner as in Examples 12-19.

[0158] The solution obtained by mixing the color developing composition, 1,3-propylene glycol and water was evaluated. The results of the immediate color development evaluation, the color development stability evaluation and the layer structure formation state evaluation are shown in Tables 9 and Fig. 9 ( Fig. 9 , the upper figure is a front view and the lower figure is a vertical view).

[0159] Table 9

[0160]

[0161]

[0162] From Table 9 and Fig. 9From the results, it can be seen that Examples 22-26 use different non-ionic surfactant contents and different ionic surfactant contents, and the instant color development evaluation is qualified (good or excellent), the color development stability evaluation is qualified (good or excellent), and the layered structure formation state evaluation has polarization phenomenon. Compared with Example 22, when the mass percentage of the color development composition in water is too low (that is, the dilution ratio of the color development composition with water is too large), the instant color development evaluation is unqualified (very poor), and the layered structure formation state evaluation has no polarization phenomenon. Compared with Example 25, when the mass percentage of the color development composition in water is too high (that is, the dilution ratio of the color development composition with water is too small), the instant color development evaluation is unqualified (slightly poor), and the layered structure formation state evaluation has no polarization phenomenon.

[0163] The results of Examples 22-26 and Comparative Examples 15-16 show that when the color-developing composition is added to water for color development, an appropriate amount of the color-developing composition added is helpful for color development.

[0164] Embodiment 27

[0165] A concentrated color-developing composition comprises the following components in percentage by weight: a) 60.64% of polyglycerol-2 laurate; b) 36.61% of propylene glycol laurate; c) 1334% of sodium di(laurylamide glutamine) lysine; and d) 2.29% of water. In the concentrated color-developing composition, the overall HLB value of component a) and component b) is 7.247.44, and the total weight of component a) and component b) is 729 times the weight of component c).

[0166] The preparation method of the concentrated color developing composition is as follows:

[0167] S1: weigh the raw materials in proportion;

[0168] S2: Put non-ionic surfactant (component a) and component b)) into the main pot;

[0169] S3: Heat to above 75°C while stirring, continue stirring for 10 minutes to make sure the material is uniform;

[0170] S4: Cooling in a water bath to 35-40°C, adding an ionic surfactant (component c)) and water;

[0171] S5: Stir until uniform.

[0172] The concentrated color-developing composition prepared in this example was diluted with water at different dilution multiples, and the dilution multiples were shown in Table 10, and the color development was observed. The results of the immediate color development evaluation, the color development stability evaluation, and the layered structure formation state evaluation are shown in Table 10.

[0173] Table 10

[0174]

[0175]

[0176] From the results in Table 10, it can be seen that when the dilution ratio is between 25 and 200, the instant color development evaluation is qualified (good or excellent), the color development stability evaluation is qualified (good or excellent), and the layered structure formation state evaluation has polarization phenomenon; especially when the dilution ratio is between 50 and 67, the instant color development evaluation is qualified (excellent) and the color development stability evaluation is qualified (excellent). When the dilution ratio is greater than 200, the instant color development evaluation is unqualified (slightly worse), and the layered structure formation state evaluation has no polarization phenomenon; when the dilution ratio is less than 25, the instant color development evaluation is unqualified (slightly worse or extremely worse), and the layered structure formation state evaluation has no polarization phenomenon.

[0177] The results in Table 10 show that when the concentrated color-developing composition is used, a dilution ratio of water between 25 and 200 is beneficial to color development, and a more preferred dilution ratio is between 50 and 67 times.

[0178] Visible light is usually separated by wavelength using a prism, and we can see that each wavelength of visible light is perceived by the human eye as light of a different color. The colors of visible light of each wavelength are purple, blue, cyan, green, yellow, orange, and red. Arranged from the shortest wavelength, they are usually called seven colors. The relationship between wavelength and color is as follows Fig.10 shown.

[0179] This example further explores the color development effects of different color development composition addition ratios. Fig.11 As shown, the color developing composition is pressed Fig.11 The solution formed by mixing the mass percentage of 0.5% to 2.5% of the surfactant in the present invention with water (99.5% to 97.5%) shows different colors. This shows that the surfactant used in the present invention forms a layered structure in a low-concentration aqueous solution, and the arrangement of the bimolecular membrane is within a specific range, which can show a variety of different colors of visible light.

[0180] Because light has the phenomena of transmission, reflection and interference, a colorful situation can be observed, and this phenomenon can also be observed in part of the color developing preparation of this embodiment. Fig.11 A is a darkroom photo (front view); Fig.11 B is a darkroom photo (vertical); Fig.11 C is a photo taken in a dark room with the light source facing the front (side view); Fig.11 D is a photo taken in a dark room with the light source at the back (front view); Fig.11 E is a photo taken with polarized light in a dark room (front view); Fig.11 F is a photo taken in a dark room with the light source at the bottom (vertical); Fig.11It can be seen that the phenomena observed from different angles are different; the color seen by the front reflected light and the color seen by the back transmitted light are two different colors of light in a complementary color relationship; the concentrated color-developing composition of this embodiment presents a liquid crystal-specific texture under the polarizing plate, as brilliant as fire.

[0181] Embodiment 28

[0182] Example 28 provides a color development composition, which includes a nonionic surfactant (a) polyglycerol-2 laurate and b) propylene glycol laurate), and also includes c) anionic surfactant. The specific raw materials used in the color development composition of Examples 28-29 are shown in Table 11. The color development compositions prepared in Example 28 and the polyol (1,3-propylene glycol) are added to water according to the mass percentages shown in Table 11, and the color development is observed in the same manner as in Examples 12-19. The solution after mixing the color development composition, 1,3-propylene glycol and water is evaluated, and the results of the instant color development evaluation, color development stability evaluation, layered structure formation state evaluation and moisturizing efficacy evaluation are shown in Table 11.

[0183] Table 11

[0184]

[0185] As can be seen from the results of Table 11, the instant color development evaluation of the color development composition prepared in Example 13 is qualified (excellent), the color development stability evaluation is qualified (excellent), and the layered structure formation state evaluation has polarization phenomenon. In addition, the moisturizing effect evaluation of the color development composition prepared in Example 13 is that the growth rate of the moisture content of the stratum corneum of the skin is ≥10% after 4 hours (the growth rate of the moisture content of the stratum corneum of the skin reaches 19.85% after 4 hours, and the growth rate of the moisture content of the stratum corneum of the skin reaches 7.35% after 8 hours). Therefore, the color development composition prepared by the present invention also has a very good moisturizing effect.

[0186] It should be noted that the color-developing compositions prepared in other embodiments of the present invention also have very good moisturizing effects, which will not be provided one by one in the present invention.

[0187] Application Examples

[0188] The concentrated color-developing composition prepared in Example 27 was mixed with active substances, polyols, and water to prepare corresponding products. The raw material compositions of the products are shown in Table 12. The obtained products all had brilliant colors.

[0189] Table 12

[0190]

[0191] The present invention has many specific application paths, and the above is only a preferred embodiment of the present invention. It should be pointed out that the above embodiments are only used to illustrate the present invention, and are not used to limit the protection scope of the present invention. For those of ordinary skill in the art, without departing from the principle of the present invention, several improvements can also be made, and these improvements should also be regarded as the protection scope of the present invention.

Claims

1. A color developing composition, characterized in that Includes the following components: a) polyglycerol fatty acid esters; b) at least one of polyol fatty acid esters and alkyl glyceryl ethers; c) at least one of anionic surfactants and cationic surfactants.

2. The color developing composition according to claim 1, characterized in that The glycerol group of the polyglycerol fatty acid ester has any degree of polymerization, and the number of carbon atoms of the fatty acid therein is 8 to 18; and / or A part or all of the hydroxyl groups in the polyglycerol fatty acid ester are esterified.

3. The color developing composition according to claim 1, characterized in that The fatty acid carbon number of the polyol fatty acid ester or alkyl glyceryl ether is 8 to 18; and / or The hydrophilic group of the polyol fatty acid ester or alkyl glyceryl ether has 2 to 6 carbon atoms; and / or A part or all of the hydroxyl groups in the polyol fatty acid ester or alkyl glyceryl ether are esterified or etherified.

4. The color developing composition according to claim 1, characterized in that The anionic surfactant is at least one of a single-chain anionic surfactant and a Gemini anionic surfactant.

5. The color developing composition according to claim 4, characterized in that The single-chain anionic surfactant includes at least one of sodium methyl cocoyl taurate and fatty acid salt; The Gemini anionic surfactant includes at least one of sodium di(laurylamide glutamine) lysine and sodium di(laureth-10) phosphate; The cationic surfactant includes distearyl dimethyl ammonium chloride.

6. The color developing composition according to any one of claims 1 to 5, characterized in that The overall HLB value of the component a) and the component b) ranges from 7.0 to 8.

5.

7. The color developing composition according to claim 1, characterized in that The total mass of the components a) and b) is 57 to 2125 times the mass of the component c).

8. The color developing composition according to claim 1, characterized in that It also includes other components; the other components are selected from at least one of polyols, chelating agents, oils, fatty alcohols, fatty acids, flavors, preservatives, amino acids, vitamins and their derivatives, amphiphilic substances, and water.

9. A method for developing color according to the color developing composition according to any one of claims 1 to 8, characterized in that: The method comprises the following steps: adding the color developing composition into water for dilution; Wherein, when water is used for dilution, the dilution multiple of water is 25 to 200 times the total mass of components a), b) and c) in the color developing composition.

10. Use of the color developing composition according to any one of claims 1 to 9 in preparing color developing cosmetics, mouthwashes or food and beverages.

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