Transparent cleaning agent

By using an aqueous reverse micelle composition and specific polyglycerol-based surfactants and aliphatic alcohols/fatty acids, the problem of transparent detergents losing transparency and stability after being exposed to water is solved, achieving high cleaning power and stability in multiple environments.

CN120641075APending Publication Date: 2025-09-12KOSE CORPORATION

Patent Information

Application Number
CN202480010162.5
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Priority Date
2023-02-03
Filing Date
2024-01-30
Publication Date
2025-09-12

AI Technical Summary

Technical Problem

Existing transparent detergents lose their transparency and cleaning power when they contain water, and their stability in high and low temperature environments is insufficient, making it difficult to meet the needs of use in multiple environments.

Method used

The aqueous reverse micelle composition is used in combination with a specific polyglycerol-based surfactant and aliphatic alcohols and/or fatty acids that are liquid at 25°C to form a stable reverse micelle structure, ensuring that the detergent maintains transparency in the presence of water and is stable at high and low temperatures.

Benefits of technology

Even with water, the clear cleaner maintains its appearance transparency and high cleaning power, and remains stable over a wide temperature range, making it suitable for storage and use in various environments.

✦ Generated by Eureka AI based on patent content.

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Abstract

The present invention addresses the problem of providing a novel transparent cleaning agent having high cleaning power and excellent long-term stability even when containing water. The transparent cleaning agent for solving the problem of the present invention is characterized by being of a water-containing reverse micelle type containing the following components (A) to (F). (A) an ester of a fatty acid having 8-10 carbon atoms and a polyglycerol; (B) an ester of a branched fatty acid having 14-22 carbon atoms and / or an unsaturated fatty acid and a polyglycerol; (C) an aliphatic alcohol and / or fatty acid that is liquid at 25 DEG C; (D) an oil agent (excluding component (C)) containing a hydrocarbon oil; (E) more than 0% and 10% by mass or less of water; and (F) a polyol.
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Description

Technical Field

[0001] The present invention relates to an aqueous reverse micelle type transparent cleaning agent. Background Art

[0002] Cleansers for removing makeup, such as foundation and lipstick, consist of an oil to dissolve the makeup's components, a solvent, and a high-HLB nonionic surfactant to remove them. Oil cleansers, in particular, are characterized by their transparent appearance and rapid blending into makeup, thanks to the stable blending of nonionic surfactants within the oil. They are also known to have excellent cleansing power.

[0003] However, these conventional oil cleansers contain high-HLB nonionic surfactants. Therefore, when used with wet hands or if water is added to the container, they form an oil-in-water emulsion, losing their apparent transparency. Furthermore, they have issues with rapid blending with makeup and reduced cleansing power.

[0004] Therefore, to date, as transparent cleansers that are strongly resistant to water intrusion, transparent cleansers containing polyglycerol-based surfactants (for example, see Patent Document 1) and transparent cleansers utilizing a bicontinuous phase consisting of a bicontinuous phase of water and oil (for example, see Patent Document 2) have been developed.

[0005] Prior art literature

[0006] Patent Literature

[0007] Patent Document 1: Japanese Patent Application Laid-Open No. 2018-070481

[0008] Patent Document 2: Japanese Patent Application Laid-Open No. 2010-280643 Summary of the Invention

[0009] Problems to be solved by the invention

[0010] Cleansers are stored in various environments, both inside and outside the bathroom. Therefore, their functionality as a cleanser depends not only on their quick integration with makeup and cleaning power, but also on their stability over time in high and low temperature environments.

[0011] The technology of Patent Document 1 shows that even with the addition of water, cleansing power is not easily reduced. However, it is unclear whether transparency and temporal stability are maintained in a state where a water phase is pre-existing. The technology of Patent Document 2 maintains the bicontinuous phase even with the addition of a small amount of water, thus maintaining rapid integration with makeup. However, compared to so-called oil-based cleansers, the cleansing power is often unsatisfactory, and it is also difficult to ensure the temporal stability of the bicontinuous phase itself.

[0012] Therefore, an object of the present invention is to provide a novel transparent detergent having high cleaning power similar to that of an oil-based detergent and excellent stability over time even when containing water.

[0013] Means used to solve problems

[0014] In light of this reality, the present inventors conducted intensive research and, as a result, focused on aqueous reverse micelle compositions as a new formulation that is highly resistant to water intrusion and exhibits a transparent appearance. Furthermore, they discovered that by combining a specific polyglycerol-based surfactant with aliphatic alcohols and / or fatty acids that are liquid at 25°C, the composition maintains transparency even when a large amount of water is added. Furthermore, the reverse micelles exhibit excellent temperature stability over time at both high and low temperatures, resulting in the completion of the cleanser of the present invention.

[0015] That is, the present invention provides the following technical solutions.

[0016] [1] An aqueous reverse micelle type transparent detergent comprising the following components (A) to (F).

[0017] (A) esters of fatty acids having 8 to 10 carbon atoms and polyglycerol;

[0018] (B) esters of branched fatty acids and / or unsaturated fatty acids having 14 to 22 carbon atoms and polyglycerol;

[0019] (C) aliphatic alcohols and / or fatty acids that are liquid at 25°C;

[0020] (D) an oil containing hydrocarbon oil (excluding component (C));

[0021] (E) water exceeds 0 and is 10% by mass or less;

[0022] (F) Polyol.

[0023] [2] The transparent cleaning agent according to [1], wherein the component (C) is decyltetradecyl alcohol and / or isostearic acid.

[0024] [3] The transparent cleaning agent according to [1] or [2], wherein the ratio (E) / [(A)+(B)] of the content of the component (E) to the total content of the components (A) and (B) is 0.1 to 0.5.

[0025] Effects of the Invention

[0026] The transparent cleanser of the present invention maintains its transparency and feel even when mixed with water, such as when used with wet hands, maintaining high cleaning power. Furthermore, its excellent temporal stability over a wide temperature range allows for storage in various environments. Furthermore, since the transparent cleanser of the present invention is an aqueous reverse micelle, it can contain water-soluble active ingredients, and can also be expected to achieve cleansing and beauty effects from the aqueous phase itself. DETAILED DESCRIPTION

[0027] Hereinafter, embodiments of the present invention will be described. However, the present invention is not limited to the following embodiments. In this specification, "X to Y" indicating a range includes both X and Y and means "X or more and Y or less."

[0028] In this specification, "transparent" means a transmittance of 90.0% or greater for light with a wavelength of 500 nm. The transmittance is measured using a UV-visible spectrophotometer (UV-2600, manufactured by Shimadzu Corporation) using a quartz cuvette with an optical path length of 10 mm and an optical path width of 10 mm and water as a blank (transmittance of 100%).

[0029] In this specification, "liquid at 25°C" means having fluidity at 1 atmosphere and 25°C, and does not include paste-like or semi-solid oils. Volatility and non-volatility are not particularly limited.

[0030] Ingredient (A): Ester of fatty acid with 8 to 10 carbon atoms and polyglycerol

[0031] Component (A) used in the present invention is an ester obtained by esterifying a fatty acid having 8 to 10 carbon atoms with a polyglycerol obtained by polymerizing glycerol. It is not particularly limited as long as it is an ingredient commonly used in cosmetics, quasi-drugs, etc. The fatty acid used in the esterification is a linear or branched saturated or unsaturated fatty acid having 8 to 10 carbon atoms. The polyglycerol preferably has a degree of polymerization of glycerol of 4 to 10, more preferably 6 to 8. From the perspective of forming aqueous reverse micelles, the ester is preferably a diester in which two fatty acid molecules are added to the polyglycerol. Component (A) can be selected and used as needed, but the average HLB is preferably 8 to 12. Specifically, for example, a diester of a saturated fatty acid having 10 carbon atoms and a polyglycerol having a degree of polymerization of 6, namely, polyglyceryl dicaprate-6 (HLB = 10.2), is mentioned. A commercially available product thereof is SUNSOFT Q-102H-C (manufactured by Sun Chemical Co., Ltd.).

[0032] In the present invention, HLB (Hyrdrophile-Lipophile Balance) is an index showing the balance between hydrophilicity and lipophilicity, and is calculated using the following (Formula 1) based on Oda Teramura et al., and the average HLB is set as a weighted average.

[0033] HLB = "Inorganic value (IV) / Organic value (OV)" × 10... (Formula 1)

[0034] (See "Organic Concept Map - Fundamentals and Applications" by Yoshio Koda, pp. 11-17, Sankyo Publishing, 1984)

[0035] The content of component (A) in the present invention is not particularly limited. From the perspective of forming aqueous reverse micelles, it is preferably 5% by mass (hereinafter abbreviated as "%) or more of the total amount of the transparent detergent, more preferably 8% or more, and even more preferably 12% or more. Furthermore, it is preferably 25% or less, more preferably 20% or less, and even more preferably 17% or less. Furthermore, the content of component (A) is preferably 5-25%, more preferably 8-20%, and even more preferably 12-17%. Within this range, excellent temporal stability and cleaning power are achieved, making it more preferred.

[0036] Component (B): ester of branched fatty acid and / or unsaturated fatty acid with 14 to 22 carbon atoms and polyglycerol

[0037] The component (B) used in the present invention is an ester obtained by esterifying a branched fatty acid and / or an unsaturated fatty acid having 14 to 22 carbon atoms with a polyglycerol obtained by polymerizing glycerol. There are no particular limitations on the component as long as it is a component commonly used in cosmetics, quasi-drugs, etc. The fatty acid used in the esterification has 14 to 22 carbon atoms. Specifically, as a branched fatty acid, isopalmitic acid, isostearic acid, etc. can be listed, and as an unsaturated fatty acid, oleic acid, linoleic acid, linolenic acid, etc. can be listed. As a polyglycerol, the degree of polymerization of glycerol is preferably 4 to 15, and more preferably 6 to 10. As an ester, a monoester or a diester is preferred. One or more components (B) can be selected and used as needed, and the average HLB is preferably 10 to 15. Specific examples include polyglyceryl dioleate-10 (HLB = 11.9), a diester of polyglycerol having a polymerization degree of 10 with an unsaturated fatty acid having 18 carbon atoms and glycerol; polyglyceryl diisostearate-10 (HLB = 10), a diester of polyglycerol having a polymerization degree of 10 with a branched fatty acid having 18 carbon atoms and glycerol; and polyglyceryl isostearate-10 (HLB = 12), an ester of polyglycerol having a polymerization degree of 10 with a branched fatty acid having 18 carbon atoms and glycerol. Commercially available products include SUNSOFT Q-172Y-C (manufactured by Taiyo Chemical Co., Ltd.), NIKKOL DECAGLYN 2-ISV (manufactured by Nikko Chemical Co., Ltd.), and NIKKOL DECAGLYN 1-ISV (manufactured by Nikko Chemical Co., Ltd.).

[0038] The content of component (B) in the present invention is not particularly limited. From the perspective of temporal stability, it is preferably 1% or more, more preferably 2% or more, of the total amount of the clear detergent. Furthermore, it is preferably 12% or less, more preferably 10% or less. Furthermore, the content of component (B) is preferably 1-12%, more preferably 2-10%. Within this range, there is no precipitation at low temperatures or separation at high temperatures, resulting in excellent temporal stability and cleaning power, making it more preferred.

[0039] In the present invention, although not particularly limited, the content of component (B) is preferably less than that of component (A). For example, the ratio (A) / (B) of the content of component (A) to the content of component (B) is preferably 1.5 to 6. Within this range, aqueous reverse micelles can be stably formed.

[0040] Ingredient (C): Fatty alcohol and / or fatty acid that is liquid at 25°C

[0041] Component (C) used in the present invention is an aliphatic alcohol and / or fatty acid that is liquid at 25°C. There are no particular limitations as long as it is a component commonly used in cosmetics, quasi-drugs, etc. For example, aliphatic alcohols and / or fatty acids having 12 to 30 carbon atoms, linear or branched, saturated or unsaturated hydrocarbon groups, together with components (A) and (B) in the present invention contribute to the formation of aqueous reverse micelles. Specifically, oleyl alcohol, isostearyl alcohol, octyldodecanol, decyltetradecyl alcohol, oleic acid, linoleic acid, linolenic acid, isopalmitic acid, and isostearic acid can be used. Component (C) can be selected and used alone or in combination, and from the perspective of forming aqueous reverse micelles, decyltetradecyl alcohol and isostearic acid are preferred. Commercially available products include Isostearic Acid EX (manufactured by Advanced Alcohol Industries, Ltd.), NAA-400 Oleic Acid (manufactured by NOF Corporation), and Risonol 24SP (manufactured by Advanced Alcohol Industries, Ltd.).

[0042] The content of component (C) in the present invention is not particularly limited. However, from the perspective of forming aqueous reverse micelles, it is preferably 0.1% or more, more preferably 0.5% or more, of the total amount of the clear detergent. Furthermore, it is preferably 10% or less, more preferably 8% or less. Furthermore, the content of component (C) is preferably 0.1-10%, more preferably 0.5-8%. Within this range, aqueous reverse micelles are formed, resulting in excellent stability over time and cleaning power, making it more preferred.

[0043] Ingredient (D): Oil containing hydrocarbon oil

[0044] Component (D) used in the present invention is an oil containing a hydrocarbon oil. It is not particularly limited as long as it is a component commonly used in cosmetics, quasi-drugs, etc. For example, regardless of its properties such as volatility, non-volatility, solid state, liquid state, or origin such as animal oil, vegetable oil, or synthetic oil, examples include hydrocarbons, fats and oils, ester oils, fatty acids, higher alcohols, silicone oils, and fluorinated oils, excluding components (A), (B), or (C) described above. Component (D) can be selected and used as needed. As for the properties of component (D) as a whole, it is preferably liquid at 25°C.

[0045] Specific examples of the hydrocarbon oil as component (D) include isododecane, isohexadecane, light mobile isoparaffin, liquid paraffin, heavy mobile isoparaffin, α-olefin oligomers, squalane, vaseline, polyisobutene, and polybutene. In addition, examples of other components (D) include plant oils and fats such as olive oil, castor oil, mink oil, macadamia oil, avocado oil, and meadowfoam oil; jojoba oil, diisobutyl adipate, 2-hexyldecyl adipate, di(2-heptylundecanyl) adipate, alkyl glycol monoisostearate, isocetyl isostearate, trimethylolpropane triisostearate, ethylene glycol di-2-ethylhexanoate, neopentyl glycol di-2-ethylhexanoate, trimethylolpropane tri-2-ethylhexanoate, pentaerythritol tetra-2-ethylhexanoate, cetyl 2-ethylhexanoate, oleyl oleate, Octyldodecyl oleate, decyl oleate, neopentyl glycol dicaprate, propylene glycol dicaprate, triethyl citrate, 2-ethylhexyl succinate, isocetyl stearate, butyl stearate, diisopropyl sebacate, di(2-ethylhexyl) sebacate, cetyl lactate, myristyl lactate, isopropyl palmitate, 2-ethylhexyl palmitate, 2-hexyldecyl palmitate, 2-heptylundecyl palmitate, dipentaerythritol fatty acid ester, isononyl isononanoate, isotridecyl isononanoate, isopropyl myristate, isopropyl palmitate, 2-octyldodecyl myristate, 2-Hexyldecyl myristate, myristyl myristate, hexyldecyl dimethyloctanoate, ethyl laurate, hexyl laurate, 2-ethylhexyl methoxycinnamate, diisostearyl malate, tri-2-ethylhexanoin, tri(caprylic acid / capric acid)glyceryl, tricaprin, triisostearate, diisostearate, diisostearate, tetraisostearate, decaisostearate, triisopalmitin, trimyristin, myristyl isostearate, etc. Glyceryl fatty acid monoglycerides or glycerol having a polymerization degree of 3 The following fatty acid polyglycerol esters; ester oils such as tridecyl trimellitate, 2-octyldodecyl N-lauroyl-L-glutamate, and di(phytosteryl 2-octyldodecyl) N-lauroyl-L-glutamate; fatty acids such as myristic acid and stearic acid; higher alcohols such as stearyl alcohol; silicone oils such as low-polymerization degree dimethylpolysiloxane, high-polymerization degree dimethylpolysiloxane, methylphenylpolysiloxane, decamethylcyclopentasiloxane, octamethylcyclotetrasiloxane, and fluorine-modified organopolysiloxane; fluorine-based oils such as perfluorodecane, perfluorooctane, and perfluoropolyether.

[0046] In the present invention, from the perspective of forming aqueous reverse micelles, component (D) must contain at least a hydrocarbon oil, more preferably an ester oil and a hydrocarbon oil, and even more preferably, consists solely of an ester oil and a hydrocarbon oil. The content of the hydrocarbon oil in component (D) is preferably 3 to 50% of the total amount of the clear detergent.

[0047] The content of component (D) in the present invention is not particularly limited. From the perspective of aqueous reverse micelle formation and temporal stability, the content of component (D) is preferably 50% or more, more preferably 60% or more, and even more preferably 70% or more of the total amount of the transparent detergent. Furthermore, it is preferably 85% or less, preferably 80% or less, and even more preferably 75% or less. Furthermore, the content of component (D) is preferably 50-85%, more preferably 60-80%, and even more preferably 70-75%. Within this range, aqueous reverse micelles are formed, resulting in excellent temporal stability and cleaning power, making it more preferred.

[0048] Ingredients (E): Water

[0049] The ingredients used in the present invention are not particularly limited as long as they are commonly used in cosmetics, quasi-drugs, etc. Component (E) includes, for example, purified water, hot spring water, ion-exchanged water, deep water, or plant steam distilled water, and one or more of these can be selected and used as needed. Furthermore, in the present invention, component (E) also functions as a solvent for water-soluble active ingredients. By dissolving, for example, the hot spring ingredients, plant extracts, and salts, it can impart cosmetic benefits such as the warming effect of carbonic acid and the keratolytic effect of alkali.

[0050] From the perspective of forming aqueous reverse micelles, the content of component (E) in the present invention is greater than 0% and less than 10% of the total amount of the transparent detergent. If component (E) exceeds 10%, aqueous reverse micelles may not form. Furthermore, it is preferably at least 1% of the total amount of the transparent detergent, and more preferably at least 3%. Furthermore, it is preferably at most 8%, and more preferably at most 5%. Furthermore, the content of component (E) is preferably 1-10%, and more preferably 3-8%. Within this range, aqueous reverse micelles are formed, resulting in excellent stability over time and cleaning power, making it more preferred.

[0051] In the present invention, although not particularly limited, the ratio of the content of component (E) to the total content of components (A) and (B) (E) / [(A) + (B)] is preferably 0.1 or greater, more preferably 0.2 or greater. Furthermore, it is preferably 0.7 or less, and more preferably 0.5 or less. Furthermore, the ratio is preferably 0.1 to 0.7, more preferably 0.1 to 0.5%, and even more preferably 0.2 to 0.5%. Within this range, aqueous reverse micelles can be stably formed, which is preferred.

[0052] In the present invention, the ratio (C) / (E) of the content of component (C) to the content of component (E) is not particularly limited, but is preferably 0.1 to 3, more preferably 0.3 to 1, from the viewpoint of temporal stability and formation of aqueous reverse micelles.

[0053] Ingredient (F): Polyol

[0054] The component (F) used in the present invention is not particularly limited as long as it is an ingredient commonly used in cosmetics, quasi-drugs, etc. In the present invention, it is preferably liquid at 25°C from the viewpoint of contributing to the formation of aqueous reverse micelles and temporal stability together with components (A) and (B). Examples include 1,3-butylene glycol, 1,2-pentanediol, 1,2-hexanediol, propylene glycol, dipropylene glycol, tripropylene glycol, polypropylene glycol, glycerol, diglycerol, polyglycerol, 1,2-octanediol, polyethylene glycol, and sorbitol. One or more of these can be selected and used as needed. Among these, one or more of the components selected from 1,3-butylene glycol, dipropylene glycol, and glycerol are also preferred from the viewpoint of feel in use and stability.

[0055] The content of component (F) in the present invention is not particularly limited. However, from the perspective of temporal stability, it is preferably 0.1% or more, more preferably 0.5% or more, and even more preferably 1% or more of the total amount of the clear detergent. Furthermore, it is preferably 5% or less, and more preferably 3% or less. Furthermore, the content of component (F) is preferably 0.1-5%, and more preferably 0.5-3%. Within this range, aqueous reverse micelles are formed, resulting in excellent temporal stability and cleaning power, making it more preferred.

[0056] In addition to the essential ingredients described above, the transparent cleanser of the present invention may contain, as needed, ingredients commonly used in cosmetics within the quantitative and qualitative ranges that do not impair the effects of the present invention. For example, in addition to components (A) and (B), surfactants, water-soluble polymers, moisturizers, pH adjusters, cosmetic ingredients, preservatives, fragrances, and cooling agents may be contained.

[0057] The transparent cleanser of the present invention can be implemented in various forms, such as liquid, gel, and semisolid. However, from the perspective of further exerting the effects of the present invention, a liquid form is preferred. Here, the term "liquid" refers to a substance having a viscosity of 15,000 mPa·s or less, preferably 10,000 mPa·s or less, more preferably 7,000 mPa·s or less, and even more preferably 5,000 mPa·s or less, as measured at 25°C using a Brookfield rotational viscometer.

[0058] The production method is not particularly limited and can be prepared by a conventional method. For example, components (A) to (D) and components (E) and (F) are uniformly mixed and dissolved, and then the mixture is mixed.

[0059] The transparent cleanser of the present invention can be applied to cleansers, facial cleansers, shampoos, body soaps, hand soaps, massage products, scrubs, etc. From the viewpoint of being able to actually feel the effects of the present invention, cleansers and facial cleansers are preferred.

[0060] Example

[0061] Examples 1 to 19 and Comparative Examples 1 to 7: Cleaning Agents

[0062] Cleaning agents having the compositions shown in Table 1 below were prepared by the following production method. Transparency, formation of aqueous reverse micelles, detergency, and temporal stability were evaluated according to the following evaluation methods and criteria. The results are shown in Table 1. For samples with a transparency rating of "×," subsequent evaluation was omitted.

[0063] [Table 1]

[0064]

[0065] (Manufacturing Method)

[0066] A: Mix No. 1 to 12 uniformly.

[0067] B: Mix No. 13 to 17 uniformly.

[0068] C: A clear detergent obtained by mixing A and B.

[0069] [Evaluation Method 1] Transparency

[0070] After preparing each sample of Examples 1 to 19 and Comparative Examples 1 to 7, the solubilization state was visually observed.

[0071] (Judgment Criteria)

[0072] [Judgment]: [Evaluation]

[0073] ○: Transparent single phase

[0074] ×: Separation confirmed (two phases)

[0075] [Evaluation Method 2] Formation of Aqueous Reverse Micelle

[0076] Each sample of Examples 1 to 19 and Comparative Examples 1 to 7 was placed in a glass container, and a small amount of an aqueous solution of an aqueous dye (Blue No. 1) was added dropwise thereto. The solution was then allowed to stand at 25°C for 1 hour. Each sample was then visually observed to determine whether aqueous reverse micelles had formed based on the dispersion of the aqueous dye.

[0077] (Judgment Criteria)

[0078] [Judgment]: [Evaluation]

[0079] ○: Precipitation of the aqueous dye was observed (aqueous reverse micelles were formed)

[0080] ×: The aqueous dye was dispersed throughout the entire sample (a bicontinuous phase was formed).

[0081] [Evaluation method 3] Cleaning power

[0082] Twenty cosmetics evaluation panelists applied the following water-in-oil liquid foundation to their forearms and, one hour later, performed a use test on the cleansers of Examples 1-19 and Comparative Examples 1-7. For this use test, the makeup-applied forearm and the other hand were lightly moistened, and a cherry-sized amount of each sample was blended. After rinsing with warm water, the speed of blending into the makeup was evaluated on a five-point scale based on the following evaluation criteria. The average score of all panelists' evaluations was then determined for each sample using the following criteria.

[0083] Water-in-oil liquid foundation (makeup example)

[0084]

[0085]

[0086] (Note 1) Dimethylpolysiloxane (20CS) 2% treatment (manufacturing method)

[0087] (A) Mix components 1 to 3 uniformly.

[0088] (B) Components 4 to 10 were uniformly dispersed using a roller.

[0089] (C) Add (B) to the above (A) and mix well.

[0090] (D) Components 11 to 16 are added to the above (C) and emulsified to obtain a water-in-oil liquid foundation.

[0091] (Evaluation Criteria)

[0092] [Rating]: [Evaluation results]

[0093] 5 points: Very good

[0094] 4 points: Good

[0095] 3 points: I can’t tell

[0096] 2 points: slightly bad

[0097] 1 point: Not good (judgment standard)

[0098] [Judgment]: [Average score]

[0099] ◎:4.0 points or above

[0100] ○: 3.5 points or more and less than 4.0 points

[0101] △: 2.0 points or more and less than 3.5 points

[0102] ×: Less than 2.0 points

[0103] [Evaluation Method 4] Stability over time

[0104] Each sample of Examples 1 to 19 and Comparative Examples 1 to 7 was placed in a glass container, sealed, and stored in a thermostatic bath at 50°C and 5°C for 4 weeks, respectively. The state of each sample was then visually observed after returning to room temperature (25°C) and evaluated according to the following criteria.

[0105] (Judgment Criteria)

[0106] [Judgment]: [Evaluation]

[0107] ◎: No separation was observed (a homogeneous and transparent single phase was maintained)

[0108] ○: Slight separation was observed

[0109] ×: Separation confirmed

[0110] The results in Table 1 clearly show that the cleaning agents of Examples 1 to 19 of the present invention are excellent in cleaning power and temporal stability at various temperatures.

[0111] In contrast, in Comparative Examples 1 and 3, which do not contain component (A) or component (C), the oil phase and the aqueous phase separated, and no aqueous reverse micelles were formed. Furthermore, Comparative Example 2, which does not contain component (B), exhibited poor temporal stability at various temperatures. Comparative Example 4, which does not contain hydrocarbon oil, and Comparative Example 5, in which the content of component (E) was outside the range, exhibited separation, and no aqueous reverse micelles were formed. Comparative Example 6, which does not contain component (F), exhibited poor temporal stability. Furthermore, in Comparative Example 7, in which the content of component (E) was outside the range, although a transparent single phase was observed, a bicontinuous phase was formed, resulting in poor cleaning power and temporal stability at various temperatures.

[0112] The present invention is further described in detail below with reference to the following formulation examples, but the present invention is not limited thereto. Similarly to the above examples, aqueous reverse micelles are formed, and the transparency, detergency, and stability over time at various temperatures are excellent.

[0113] Prescription Example 1:

[0114]

[0115]

[0116] Prescription Example 2:

Claims

1. An aqueous reverse micelle-type transparent detergent comprising the following ingredients (A) to (F): (A) esters of fatty acids having 8 to 10 carbon atoms and polyglycerol; (B) esters of branched fatty acids and / or unsaturated fatty acids having 14 to 22 carbon atoms and polyglycerol; (C) aliphatic alcohols and / or fatty acids that are liquid at 25°C; (D) an oil containing hydrocarbon oil, which does not include component (C); (E) water exceeds 0 and is 10% by mass or less; (F) Polyol.

2. The transparent cleaning agent according to claim 1, wherein The component (C) is decyltetradecyl alcohol and / or isostearic acid.

3. The transparent cleaning agent according to claim 1 or 2, wherein The ratio (E) / [(A)+(B)] of the content of the component (E) to the total content of the components (A) and (B) is 0.1 to 0.5.

Citation Information

Patent Citations

  • Skin cleansing composition

    JP2010280643A

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