Stick cosmetic
The rod-shaped cosmetic composition addresses mold release and hardness issues by combining specific waxes, polyurethanes, and oils, ensuring high gloss retention and improved usability.
Patent Information
- Authority / Receiving Office
- WO · WO
- Patent Type
- Applications
- Current Assignee / Owner
- KOSE HOLDINGS CORP
- Filing Date
- 2025-09-02
- Publication Date
- 2026-05-07
AI Technical Summary
Stick-type cosmetics with high gloss and soft, adhesive compositions face issues with mold release, surface scratching, and hardness loss at high temperatures, leading to poor usability and aesthetic problems.
A rod-shaped cosmetic composition combining specific ratios of wax, oil-soluble polyurethane, liquid ester oils with varying viscosities, and hydrocarbon oils, along with optional phenyl-modified silicone and semi-solid ester oils, to enhance gloss retention, mold release, and maintain hardness at high temperatures.
The composition achieves excellent gloss persistence, reduced film wrinkles, and improved mold release while preventing hardness reduction, resulting in enhanced usability and aesthetic appeal.
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Abstract
Description
Stick-type cosmetic
[0001] This invention relates to a bar-shaped cosmetic product.
[0002] Stick-type cosmetics, which are cosmetics filled into stick-shaped containers, are widely used as various types of cosmetics, including lip cosmetics. Recent consumers seem to be seeking stick-type cosmetics that have a melting texture and long-lasting high gloss. However, when realizing high gloss in cosmetics, the amount of hardening agents such as wax is reduced and highly viscous oils are added, which makes the cosmetic itself soft and highly adhesive, resulting in problems with release from filling containers such as capsules, molds, and rubber molds during filling and molding. In that case, the surface of the stick-type cosmetic may be scratched, resulting in an aesthetically unpleasing appearance. Furthermore, if it adheres strongly to the sleeve inside the container, stress is applied when extending and retracting the stick-type cosmetic, causing it to tear or crumble, resulting in poor usability. In addition, cosmetics with a soft and highly adhesive composition tend to lose hardness when exposed to high temperatures such as in summer, causing the stick-type cosmetic to chip or break, resulting in poor usability.
[0003] Therefore, various studies have been conducted to achieve both the high gloss and usability described above. For example, a rod-shaped oily cosmetic has been proposed, characterized by being made by directly filling a container with an oily cosmetic containing specific amounts of wax and hydrogenated polyisobutene (see, for example, Patent Document 1).
[0004] Japanese Patent Publication No. 2010-265255
[0005] However, while the stick-shaped oily cosmetic described in Patent Document 1 was excellent in terms of high gloss of the coated film and release properties from the mold, it did not address the lack of hardness reduction at high temperatures or the inconspicuousness of wrinkles in the coated film.
[0006] In view of the above circumstances, the inventors conducted diligent studies and, as a result, discovered a rod-shaped cosmetic composition that combines wax, oil-soluble polyurethane, a liquid ester oil with a viscosity of less than 3000 mPa·s at 25°C, a liquid ester oil with a viscosity of 3000 mPa·s or more at 25°C, and a hydrocarbon oil that is liquid at 25°C. This composition achieves excellent gloss retention and reduced wrinkles in the coated film, while also exhibiting superior release properties from the mold and no decrease in hardness at high temperatures, thus completing the present invention.
[0007] In other words, the present invention is as described below. [1] A rod-shaped cosmetic composition containing the following components (A) to (E): (A) wax (B) oil-soluble polyurethane (C) liquid ester oil having a viscosity of less than 3000 mPa·s at 25°C (D) liquid ester oil having a viscosity of 3000 mPa·s or more at 25°C (E) a hydrocarbon oil that is liquid at 25°C. [2] The rod-shaped cosmetic composition according to [1], wherein the viscosity of component (C) at 25°C is 10 mPa·s or more and less than 3000 mPa·s. [3] The rod-shaped cosmetic composition according to [1] or [2], wherein the viscosity of component (E) at 25°C is 10000 mPa·s or more and 1500000 mPa·s or less. [4] The rod-shaped cosmetic composition according to [1] or [2], further containing component (F) phenyl-modified silicone. [5] The present invention provides a stick-shaped cosmetic composition according to [1] or [2], further containing (G) a semi-solid ester oil at 25°C (excluding component (A)). [6] The present invention provides a stick-shaped cosmetic composition according to [1] or [2], which is oily. [7] The present invention provides a stick-shaped cosmetic composition according to [1] or [2], which is for use on the lips.
[0008] The present invention provides excellent quality in terms of the persistence of gloss of the coated film, the inconspicuousness of wrinkles in the coated film, release properties from the filling mold, and the absence of hardness reduction at high temperatures.
[0009] Preferred embodiments of the present invention will be described in detail below. However, the present invention is not limited to the following preferred embodiments and can be freely modified within the scope of the present invention. In this specification, percentages are expressed in mass unless otherwise specified. Also, in this specification, when a numerical range is expressed using "~", the range includes the values at both ends. Furthermore, "viscosity" in this invention refers to the value (mPa·s) calculated from measurements using a Type B rotational viscometer (Shibaura Systems Co., Ltd.) under conditions of 25°C. When viscosity has a range, the center value, which is the average value at both ends of the range, is defined as the viscosity in this invention.
[0010] Component (A) used in the present invention is a wax. It is not particularly limited as long as it is a wax that can be used in cosmetics, and may be synthetic or of natural origin. For example, one or more selected from hydrocarbon waxes, silicone waxes, ester waxes, etc., can be used. Examples of hydrocarbon waxes include natural hydrocarbon waxes such as ceresin wax, ozokerite wax, and microcrystalline wax; and synthetic hydrocarbon waxes such as Fischer-Tropsch wax, polyethylene wax, and ethylene-propylene copolymer. Examples of silicone waxes include alkyl-modified silicones. Examples of ester waxes include plant-derived ester waxes such as candelilla wax, carnauba wax, rice wax, and Japanese wax; animal-derived ester waxes such as whale wax; and mineral-derived ester waxes such as montan wax. While not particularly limited among these, hydrocarbon waxes are preferred from the viewpoint of release properties from the filler mold. Furthermore, the combined use of hydrocarbon wax and ester wax is more preferable from the viewpoint of gloss retention of the coated film.
[0011] Commercially available hydrocarbon waxes include CIREWAX 90 (manufactured by CIREBELLE), CIREWAX 80 (manufactured by CIREBELLE), and MULTIWAX W445 (manufactured by SONNEBORN, LLC). Commercially available silicone waxes include DC2503 (manufactured by Toray Dow Corning). Commercially available ester waxes include refined candelilla wax SR-3 (manufactured by Nippon Natural Products).
[0012] The content of component (A) is not particularly limited relative to the total amount of the stick-shaped cosmetic composition, but the lower limit is preferably 4% or more, more preferably 5% or more, and even more preferably 5.5% or more. The upper limit is preferably 15% or less, more preferably 13% or less, and even more preferably 8% or less. The range is preferably 4 to 15%, more preferably 5 to 13%, and even more preferably 5.5 to 8%. This range is more preferable in terms of the inconspicuousness of wrinkles in the coated film and release properties from the filling mold.
[0013] Component (B) used in the present invention is an oil-soluble polyurethane. Polyurethane is a polymer having urethane bonds obtained by the reaction of a compound having an isocyanate group and a compound having a hydroxyl group. Oil-soluble means that it is soluble in oily components. Any oil-soluble polyurethane can be used without particular limitations, but those that can dissolve in cetyl 2-ethylhexanoate at 30°C at a concentration of at least 1% are preferred.
[0014] The compounds having an isocyanate group are not particularly limited, but from the viewpoint of not reducing hardness at high temperatures, for example, 1,6-hexamethylene diisocyanate, 1,3-bis(isocyanatomethyl)benzene, 1,3-bis(isocyanatomethyl)cyclohexane, 2,4-toluenediisocyanate, and 2,6-toluenediisocyanate are examples. Among these, 1,6-hexamethylene diisocyanate is preferred.
[0015] The compound having a hydroxyl group is not particularly limited. For example, ethylene glycol, 1,2 - propanediol, 1,3 - propanediol, 1,3 - butanediol, 1,4 - butanediol, 1,5 - pentanediol, 1,6 - hexanediol, 2,2 - dimethyl - 1,3 - propanediol, 1,4 - cyclohexanedimethanol, decamethylene glycol, dodecamethylene glycol, etc. may be mentioned. Among these, from the viewpoint of no decrease in hardness at high temperatures, etc., one or more selected from the group consisting of ethylene glycol and 1,4 - butanediol are preferable.
[0016] Preferable embodiments of component (B) include the following (i) and (ii). In the present specification, "terminal" means "both terminals". (i) (a) Hydrogenated polybutadiene having an isocyanate group at the terminal and (b) HO - R 1 -OH (wherein R 3 represents a linear or branched C2 - C6 alkylene group which may have an ether bond) and a polyurethane obtained by the reaction with a glycol represented thereby. (ii) (c) Hydrogenated polybutadiene having a hydroxyl group at the terminal, (d) a diisocyanate compound, and (b) HO - R 3 -OH (wherein R 3 represents a linear or branched C2 - C6 alkylene group which may have an ether bond) and a polyurethane obtained by the reaction with a glycol represented thereby.
[0017] (a) is not particularly limited as long as it is hydrogenated polybutadiene having an isocyanate group at the terminal. For example, a compound represented by the following general formula (1) is shown.
[0018]
[0019] (In the formula, R 1 , R 2 are each independently a C1 - C6 alkylene group, n is an integer of 10 - 100, n 1 , n 2 each independently represents 0 or 1)
[0020] R 1 R 2Each independently represents the same or different C1-C6 alkylene group, and the alkylene may be linear or branched. Examples of the C1-C6 alkylene group include methylene, ethylene, n-propylene, n-butylene, n-pentylene, n-hexylene, and the like. R 1 's alkylene group is preferably a C1-C2 alkylene group. R 2 's alkylene group is preferably a C5-C6 alkylene group. The alkylene group is preferably linear. n represents an integer from 10 to 100, and a more preferable range of n is 15 to 55. n 1 、n<OO00014>Each independently represents the same or different 0 or 1.
[0021] In the hydrogenated polybutadiene moiety of the general formula (1) (the following general formula (6)), the repeating unit "C 4 H 8 " has various structures, for example, as shown in the following general formulas (7a) to (7d).
[0022]
[0023]
[0024] The hydrogenated polybutadiene moiety in the hydrogenated polybutadiene having an isocyanate group at the terminal may consist of only one type of repeating unit as exemplified above, or may contain two or more types of repeating units regularly or randomly. The repeating unit "C<000OO17>H 8 " constituting the hydrogenated polybutadiene moiety of the general formula (1) (the above general formula (6)) may have the same or different three-dimensional structures, and all structures represented by the general formula (6) for the hydrogenated polybutadiene moiety are included in the present invention. Examples of the hydrogenated polybutadiene having an isocyanate group at the terminal represented by the general formula (1) include, for example, the compound represented by the following general formula (2).
[0025]
[0026] (Here, in formula (2), n represents an integer from 10 to 100) The compound of general formula (2) is a hydrogenated polybutadiene having an isocyanate group at the end of general formula (1), R 1 is an ethylene group, R 2 is a hexamethylene group, n 1 = n 2 This corresponds to the case where the value is 1.
[0027] (b) HO-R 3 -OH (wherein, R 3 Examples of glycols represented by (where represents a linear or branched C2-C6 alkylene group which may have an ether bond) include, for example, ethylene glycol (HOCH 2 CH 2 OH), propylene glycol (HOCH 2 CH(OH)CH 3 ), 1,3-butylene glycol (HOCH 2 CH 2 CH(OH)CH 3 ), 1,4-butylene glycol (HOCH 2 CH 2 CH 2 CH 2 OH) and diethylene glycol (HOCH) 2 CH 2 OCH 2 CH 2 Examples include OH, and the following general formula (5)).
[0028]
[0029] (c) Hydrogenated polybutadiene having a hydroxyl group at the terminus is not particularly limited, but examples include compounds represented by the following general formula (3).
[0030]
[0031] (In the formula, n represents an integer between 10 and 100.)
[0032] In general formula (3), the hydrogenated polybutadiene portion (general formula (6)) has the same meaning as described above.
[0033] (d) Examples of diisocyanate compounds include 1,6-hexamethylene diisocyanate, 1,3-bis(isocyanatomethyl)benzene, 1,3-bis(isocyanatomethyl)cyclohexane, 2,4-toluenediisocyanate, and 2,6-toluenediisocyanate. Of these, 1,6-hexamethylene diisocyanate, represented by the following general formula (4), is preferred.
[0034]
[0035] (i): (a) hydrogenated polybutadiene with an isocyanate group at the terminal and (b) HO-R 3 -OH (wherein, R 3 When producing polyurethane by polyaddition of a glycol represented by (where (a) represents a linear or branched C2-C6 alkylene group which may have an ether bond), it is preferable to carry out the process in a molar ratio (a):(b) = 1:4 to 4:1, more preferably (a):(b) = 2:3 to 3:2, even more preferably 4:5 to 4:3, and even more preferably 9:10 to 10:9. In this case, the weight-average molecular weight (Mw) of (a) is preferably 1000 to 3000.
[0036] (ii): (c) hydrogenated polybutadiene with a hydroxyl group at the terminal, (d) diisocyanate compound, and (b) HO-R 3 -OH (in the formula R 3 When producing polyurethane by reaction with a glycol (wherein represents a linear or branched C2-C6 alkylene group which may have an ether bond), it is preferable to carry out the reaction with a molar ratio (c):(b) = 1:4 to 4:1, more preferably with a molar ratio (c):(b) = 2:3 to 3:2, even more preferably with a molar ratio (c):(b) = 4:5 to 4:3, and even more preferably with a molar ratio of 9:10 to 10:9.
[0037] Furthermore, the weight-average molecular weight (Mw) of the polyurethane obtained in (i) or (ii) is 10,000 to 150,000, more preferably 15,000 to 130,000, and even more preferably 20,000 to 110,000.
[0038] Furthermore, while component (B) is not particularly limited, it is preferably an oil-soluble polyurethane gel from the viewpoint of not experiencing a decrease in hardness at high temperatures. Here, an oil-soluble polyurethane gel refers to a gel that thickens and forms an elastic gel when the hydrophobic portion within the oil-soluble polyurethane molecule comes into contact with an oil. When an oil-soluble polyurethane gel is used, it is preferable that it is dispersed in a dispersion solvent such as an oil. The dispersion solvent is not particularly limited, but examples include oils, and one or more of these may be used in combination. Note that the oil used as the dispersion solvent for component (B) is also included in components (C), (D), and (E) of the present invention.
[0039] Furthermore, the dispersion solvent for component (B) is not particularly limited, but from the viewpoint of not reducing hardness at high temperatures, suitable oils include hydrocarbon oils such as dodecane, isododecane, tridecane, isotridecane, tetradecane, isotetradecane, isopentadecane, isohexadecane, liquid isoparaffin, squalane, hydrogenated polydecene, hydrogenated polyisobutene, 2-ethylhexyl stearate, octyldodecyl isonoisostearate, isostearyl isostearate, 2-ethylhexyl isostearate, isopropyl isostearate, cetyl palmitate, and 2-ethylhexyl lumitate, isopropyl palmitate, octyldodecyl myristate, isostearyl myristate, myristyryl myristate, isopropyl myristate, isostearyl laurate, hexyl laurate, octyldodecyl ricinoleate, isotridecyl isononanoate, isononyl isononanoate, stearyl 2-ethylhexanoate, isostearyl 2-ethylhexanoate, cetyl 2-ethylhexanoate, hexyldecyl 2-ethylhexanoate, cetyl caprylate, cetyl caprylate, octyldodecyl neopentanoate, Isostearyl neopentanoate, octyldodecyl oleate, oleyl oleate, ethyl oleate, octyldodecyl erucate, octyldodecyl stearoyloxystearate, isostearyl stearoyloxystearate, dioctyldodecyl stearoyl glutamate, dioctyldodecyl lauroyl glutamate, propylene glycol dicaprate, neopentyl glycol dicaprate, dipentaerythrityl tetraisostearate, diisostearyl malate, tridecyl trimellitate, polyglyceryl isostearate Polyglyceryl diisostearate, polyglyceryl triisostearate, polyglyceryl tetraisostearate, decaglyceryl decaisostearate, decaglyceryl deca-2-ethylhexanoate, caprylic / capric triglyceride, glyceryl tri-2-ethylhexanoate, glyceryl triisostearate, glyceryl trioleate, and other ester oils; vegetable oils such as coconut oil, olive oil, palm oil, macadamia nut oil, meadowfoam oil, jojoba oil, rapeseed oil, and rice bran oil; octyldodecanol; isostearyl alcohol;Examples include higher alcohols such as oleyl alcohol and jojoba alcohol.
[0040] Among these, the dispersion solvent is preferably an ester oil, more preferably one or more selected from the group consisting of glycerin fatty acid esters and polyglycerin fatty acid esters, and even more preferably one or more selected from the group consisting of cetyl 2-ethylhexanoate, polyglyceryl isostearate, polyglyceryl diisostearate, polyglyceryl triisostearate, polyglyceryl tetraisostearate, decaglyceryl decaisostearate, decaglyceryl deca-2-ethylhexanoate, caprylic / capric triglyceride, glyceryl tri-2-ethylhexanoate, glyceryl triisostearate, and glyceryl trioleate. By selecting the dispersion solvent from the above components, oil-soluble polyurethane can be efficiently dispersed in the oil, which is more preferable in terms of release properties from the packing mold and no decrease in hardness at high temperatures.
[0041] Component (B) is not particularly limited, but from the viewpoint of not experiencing hardness reduction at high temperatures, for example, if the INCI name (International Nomenclature Cosmetic Ingredient Labeling Names) is Polyurethane-1, Polyurethane-2, Polyurethane-4, Polyurethane-6, Polyurethane-7, Polyurethane-8, Polyurethane-9, Polyurethane-10, Polyurethane-11, Polyurethane-14, Polyurethane-15, Polyurethane-16, Polyurethane-21, Polyurethane e-23, Polyurethane-24, Polyurethane-26, Polyurethane-27, Polyurethane-32, Polyurethane-33, Polyurethane-34, Polyureth ane-35, Polyurethane-39, Polyurethane-40, Polyurethane-42, Polyurethane-43, Polyurethane-44, Polyurethane-45, Polyurethane thane-46, Polyurethane-48, Polyurethane-49, Polyurethane-50, Polyurethane-51, Polyurethane-52, Polyurethane-53, Polyu polyurethane-54, Polyurethane-55, Polyurethane-57, Polyurethane-58, Polyurethane-59, Polyurethane-61, Polyurethane-62, Pol yurethane-64, Polyurethane-66, Polyurethane-67, Polyurethane-74, Polyurethane-75, Polyurethane-79, Polyurethane-82, P polyurethane-85, Polyurethane-86, Polyurethane-93, Polyurethane-95, Polyurethane-96, Polyurethane-97, Polyurethane-98,Examples include (HDI / PPG / polycaprolactone) crosspolymer, (HDI / trimethylolhexyllactone) crosspolymer, (adipic acid / methylpentanediol / HDI) copolymer, (hydrogenated polybutadiene / glycol / HDI) copolymer, (1,4-butanediol / succinic acid / adipic acid / HDI) copolymer, and one or more of these can be used in combination. Among these, from the viewpoint of not experiencing a decrease in hardness at high temperatures, one or more selected from the group consisting of Polyurethane-4, Polyurethane-14, Polyurethane-44, Polyurethane-59, Polyurethane-64, Polyurethane-79, (HDI / trimethylolhexyllactone) crosspolymer, and (hydrogenated polybutadiene / glycol / HDI) copolymer are preferred, and Polyurethane-4, Polyureth One or more selected from the group consisting of ane-14, Polyurethane-79, (HDI / trimethylol hexyllactone) crosspolymer, and (hydrogenated polybutadiene / glycol / HDI) copolymer is more preferred, and one or more selected from the group consisting of Polyurethane-14, Polyurethane-79, (HDI / trimethylol hexyllactone) crosspolymer, and (hydrogenated polybutadiene / glycol / HDI) copolymer is even more preferred. Examples of commercially available products include Oilkemia 5S polymer (Lubrizol, INC. name: Tri(caprylic / capric acid) glyceryl, polyurethane-79) and Oilkemia 5S CC polymer (Lubrizol, INC. name: Tri(caprylic / capric acid) glyceryl, hydrogenated poly(C6-20 olefin), (HDI / trimethylol hexyllactone) crosspolymer).
[0042] The content of component (B) is not particularly limited relative to the total amount of the bar-shaped cosmetic composition, but the lower limit is preferably 0.1% or more, more preferably 0.15% or more, and even more preferably 0.4% or more. The upper limit is preferably 1.7% or less, more preferably 1.6% or less, and even more preferably 1.4% or less. The range is preferably 0.1 to 1.7%, more preferably 0.15 to 1.6%, and even more preferably 0.4 to 1.4%. This range is more preferable in terms of release properties from the filling mold and no decrease in hardness at high temperatures.
[0043] Component (C) used in the present invention is a liquid ester oil with a viscosity of less than 3000 mPa·s at 25°C. While not particularly limited, examples of liquid ester oils with a viscosity of less than 3000 mPa·s at 25°C include isononyl isononanoate, isotridecyl isononanoate, cetyl 2-ethylhexanoate, polyglyceryl-2 triisostearate, pentaerythrityl tetraethylhexanoate, triethylhexanoin, and diisostearyl malate. A commercially available isononyl isononanoate is Saracos 99 (manufactured by Nisshin Oillio Group, viscosity 3-7 mPa·s <center value 5 mPa·s>). A commercially available isotridecyl isononanoate is Saracos 913 (manufactured by Nisshin Oillio Group, viscosity 6-11 mPa·s <center value 8.5 mPa·s>). Commercially available cetyl 2-ethylhexanoate includes Saracos 816T (manufactured by Nisshin Oillio Group, viscosity 7-14 mPa·s <center value 10.5 mPa·s>). Commercially available polyglyceryl-2 triisostearate includes Cosmol 43V (manufactured by Nisshin Oillio Group, viscosity 350-450 mPa·s <center value 400 mPa·s>). Commercially available pentaerythrityl tetraethylhexanoate includes Saracos 5408 (manufactured by Nisshin Oillio Group, viscosity 100-125 mPa·s <center value 112.5 mPa·s>). Commercially available triethylhexanoin includes MYRITOL GTEH (manufactured by BASF, viscosity 20-30 mPa·s <center value 25 mPa·s>). Examples of commercially available diisostearyl malate include High Malate DIS (manufactured by Higher Alcohol Industry Co., Ltd., viscosity 2700 mPa·s).
[0044] Component (C) is not particularly limited, but polyglycerin fatty acid esters and organic acid alcohol esters are preferred, and polyglyceryl-2 triisostearate, triethylhexanoin, and diisostearyl malate are more preferred from the viewpoint of release properties from the packing mold.
[0045] The viscosity of component (C) at 25°C is preferably 10 mPa·s or more at the lower limit, more preferably 30 mPa·s or more, and even more preferably 50 mPa·s or more. At the upper limit, it is less than 3000 mPa·s, preferably 2900 mPa·s or less, more preferably 2700 mPa·s or less, and even more preferably 2500 mPa·s or less. Within the range, it is preferably 10 mPa·s or more and less than 3000 mPa·s, preferably 10 to 2900 mPa·s, more preferably 30 to 2700 mPa·s, and even more preferably 50 to 2500 mPa·s. Within this range, it is more preferable in terms of release properties from the filling mold and the reduced visibility of wrinkles in the coated film.
[0046] The content of component (C) is not particularly limited in relation to the total amount of the stick-shaped cosmetic composition, but the lower limit is preferably 25% or more, more preferably 29% or more, and even more preferably 33% or more. The upper limit is preferably 75% or less, more preferably 71% or less, and even more preferably 60% or less. The range is preferably 25 to 75%, more preferably 29 to 71%, and even more preferably 33 to 60%. This range is more preferable from the viewpoint of release properties from the filling mold, etc.
[0047] Component (D) used in the present invention is a liquid ester oil with a viscosity of 3000 mPa·s or more at 25°C. The liquid ester oil with a viscosity of 3000 mPa·s or more at 25°C is not particularly limited, but examples include polyglyceryl-2 isostearate, triisostearin, and dimer dilinoleyl hydrogenated rosin condensate. A commercially available polyglyceryl-2 isostearate is Cosmol 41V (manufactured by Nisshin Oillio Group, viscosity 6000-6600 mPa·s <center value 6300 mPa·s>). A commercially available triisostearin is Saracos 3318 (manufactured by Nisshin Oillio Group, viscosity 12000-14000 mPa·s <center value 13000 mPa·s>). Examples of commercially available dimer dilinoleyl hydrogenated rosin condensates include LUSPLAN DD-DHR (manufactured by Nippon Seika Co., Ltd., viscosity 33,000 mPa·s).
[0048] Component (D) is not particularly limited, but triisostearin and dimer dilinoleyl hydrogenated rosin condensate are preferred in terms of gloss retention of the coating film and reduced visibility of wrinkles in the coating film.
[0049] The viscosity of component (D) at 25°C is preferably 3,000 mPa·s or more at the lower limit, preferably 5,000 mPa·s or more, more preferably 7,000 mPa·s or more, even more preferably 10,000 mPa·s or more, and even more preferably 15,000 mPa·s or more. The upper limit is preferably 40,000 mPa·s or less, more preferably 37,000 mPa·s or less, and even more preferably 34,000 mPa·s or less. The range is preferably 3,000 to 40,000 mPa·s, 5,000 to 40,000 mPa·s, more preferably 7,000 to 37,000 mPa·s, even more preferably 10,000 to 34,000 mPa·s, and even more preferably 15,000 to 34,000 mPa·s. Within this range, it is more preferable in terms of the persistence of gloss of the coating film and the reduced visibility of wrinkles in the coating film.
[0050] The content of component (D) is not particularly limited relative to the total amount of the stick-shaped cosmetic composition, but the lower limit is preferably 3% or more, more preferably 5% or more, and even more preferably 10% or more. The upper limit is preferably 25% or less, more preferably 20% or less, and even more preferably 16% or less. The range is preferably 3 to 25%, more preferably 5 to 20%, and even more preferably 10 to 16%. Within this range, it is more preferable in terms of release properties from the filling mold, gloss retention of the coating film, and less noticeable wrinkles in the coating film.
[0051] The component (E) used in the present invention is a hydrocarbon oil that is liquid at 25°C. In the present invention, "liquid at 25°C" means that it exhibits fluidity at 25°C. The hydrocarbon oil that is liquid at 25°C is not particularly limited, but examples include isododecane, mineral oil, hydrogenated polyisobutene, and polybutene. Commercially available hydrogenated polyisobutenes include Pearlream 18 (manufactured by NOF Corporation, viscosity 40,000 mPa·s), Pearlream 24 (manufactured by NOF Corporation, viscosity 110,000 mPa·s), and Pearlream 46 (manufactured by NOF Corporation, viscosity 1,000,000 mPa·s). Commercially available polybutene products include refined polybutene HV-100F (SB) (manufactured by Nippon Natural Products Co., Ltd., viscosity 37,000 mPa·s) and Nippon Oil Polybutene HV-1900 (manufactured by ENEOS Corporation, viscosity 1,000,000 mPa·s).
[0052] Component (E) is not particularly limited, but hydrogenated polyisobutene and polybutene are preferred from the viewpoint of maintaining the gloss of the coating film and making wrinkles in the coating film less noticeable.
[0053] The viscosity of component (E) at 25°C is not particularly limited, but the lower limit is preferably 10,000 mPa·s or more, more preferably 20,000 mPa·s or more, even more preferably 30,000 mPa·s or more, and even more preferably 40,000 mPa·s or more. The upper limit is preferably 1,500,000 mPa·s or less, more preferably 1,400,000 mPa·s or less, even more preferably 1,300,000 mPa·s or less, and even more preferably 1,200,000 mPa·s or less. The range is preferably 10,000 to 1,500,000 mPa·s, more preferably 20,000 to 1,400,000 mPa·s, even more preferably 30,000 to 1,300,000 mPa·s, and even more preferably 40,000 to 1,200,000 mPa·s. Within this range, it is more preferable in terms of the persistence of gloss of the coating film and the reduced visibility of wrinkles in the coating film.
[0054] The content of component (E) is not particularly limited relative to the total amount of the stick-shaped cosmetic composition, but the lower limit is preferably 7% or more, more preferably 8% or more, and even more preferably 10% or more. The upper limit is preferably 27% or less, more preferably 25% or less, and even more preferably 20% or less. The range is preferably 7 to 27%, more preferably 8 to 25%, and even more preferably 10 to 20%. Within this range, it is more preferable in terms of release properties from the filling mold, gloss retention of the coating film, and less noticeable wrinkles in the coating film.
[0055] The mass ratio of the content of component (B) to the total content of component (A) and component (B) used in the present invention ((B) / {(A) + (B)}) is not particularly limited, but the lower limit is preferably 0.03 or more, more preferably 0.05 or more, and even more preferably 0.075 or more. The upper limit is preferably 0.2 or less, more preferably 0.15 or less, and even more preferably 0.1 or less. The range is preferably 0.03 to 0.2, more preferably 0.05 to 0.15, and even more preferably 0.075 to 0.1. This range is more preferable in terms of release properties from the filling mold, hardness reduction at high temperatures, gloss retention of the coating film, and less noticeable wrinkles in the coating film.
[0056] The mass ratio of the total content of components (D) and (E) to the content of component (A) used in the present invention ({(D) + (E)} / (A)) is preferably 2.5 or higher as a lower limit, more preferably 3.0 or higher, even more preferably 3.5 or higher, and even more preferably 4.0 or higher. As an upper limit, it is preferably 8 or lower, more preferably 7.5 or lower, even more preferably 6.5 or lower, and even more preferably 5.5 or lower. As a range, it is preferably 2.5 to 8, more preferably 3.0 to 7.5, even more preferably 3.5 to 6.5, and even more preferably 4.0 to 5.5. Within this range, it is more preferable in terms of release properties from the filling mold, gloss retention of the coating film, and less noticeable wrinkles in the coating film.
[0057] The mass ratio of the content of component (C) to the content of component (D) used in the present invention ((C) / (D)) is preferably 1.5 or more at the lower limit, more preferably 1.75 or more, and even more preferably 2.5 or more. At the upper limit, it is preferably 20 or less, more preferably 10 or less, and even more preferably 6 or less. Within the range, it is preferably 1.5 to 20, more preferably 1.75 to 10, and even more preferably 2.5 to 6. Within this range, it is more preferable in terms of release properties from the filling mold, gloss retention of the coating film, and less noticeable wrinkles in the coating film.
[0058] Furthermore, the present invention may also contain a phenyl-modified silicone as component (F). The phenyl-modified silicone used in the present invention may be any silicone having a dimethylsiloxane skeleton in which at least some of the methyl groups are substituted with phenyl groups. Examples include diphenyl dimethicone, diphenylsiloxy phenyl trimethicone, trimethylsiloxy phenyl dimethicone, and phenyl trimethicone. A commercially available example of diphenyl dimethicone is KF-54 (manufactured by Shin-Etsu Chemical Co., Ltd.). A commercially available example of diphenylsiloxy phenyl trimethicone is KF-56 (manufactured by Shin-Etsu Chemical Co., Ltd.). A commercially available example of phenyl trimethicone is SH556 FLUID (manufactured by Toray Dow Corning).
[0059] Component (F) is not particularly limited, but diphenyl dimethicone and trimethylsiloxyphenyl dimethicone are preferred from the viewpoint of release properties from the packing mold.
[0060] The content of component (F) is not particularly limited in relation to the total amount of the stick-shaped cosmetic composition, but the lower limit is preferably 5% or more, more preferably 7.5% or more, and even more preferably 10% or more. The upper limit is preferably 20% or less, more preferably 18% or less, and even more preferably 16% or less. The range is preferably 5 to 20%, more preferably 7.5 to 18%, and even more preferably 10 to 16%. This range is more preferable from the viewpoint of release properties from the filling mold, etc.
[0061] Furthermore, the present invention may contain, as component (G), a semi-solid ester oil at 25°C (excluding component (A)). In the present invention, "semi-solid at 25°C" means that it does not exhibit fluidity when stored at 25°C and deforms when stress is applied. Any semi-solid ester oil at 25°C commonly used in cosmetics can be used without particular limitation. Specifically, examples include dipentaerythrityl fatty acid esters such as hexa(hydroxystearic acid / stearic acid / rosinic acid) dipentaerythrityl, hydrogenated castor oil fatty acid esters such as hydrogenated castor oil stearate, hydrogenated castor oil isostearate, and hydrogenated castor oil hydroxystearate, cholesterol fatty acid esters such as cholesteryl hydroxystearate, phytosterol fatty acid esters such as phytosteryl oleate and phytosteryl macadamia nut oil fatty acid, hydrogenated vegetable oils such as hydrogenated coconut oil and hydrogenated palm oil, and dimer dilinoleic acid (phytosteryl / isosteryl / cetyl / stearyl / behenyl), and one or more of these can be used. A commercially available product of dimer dilinoleic acid (phytosteryl / isosteryl / cetyl / stearyl / behenyl) is PLANDOOL-S (manufactured by Nippon Seika Co., Ltd.).
[0062] Component (G) is not particularly limited, but dimer dilinoleic acid (phytosteryl / isosteryl / cetyl / stearyl / behenyl) is preferred in terms of maintaining the gloss of the coating film and making wrinkles less noticeable in the coating film.
[0063] The content of component (G) used in the present invention is not particularly limited in relation to the total amount of the stick-shaped cosmetic composition, but the lower limit is preferably 5% or more, more preferably 7.5% or more, and even more preferably 10% or more. The upper limit is preferably 20% or less, more preferably 18% or less, and even more preferably 16% or less. The range is preferably 5 to 20%, more preferably 7.5 to 18%, and even more preferably 10 to 16%. This range is more preferable in terms of the persistence of gloss of the coated film and the reduced visibility of wrinkles in the coated film.
[0064] In addition to the above-mentioned components (A) to (G), the stick-shaped cosmetic composition of the present invention may appropriately contain components commonly used in cosmetics, such as polymers other than component (B), oily components other than components (A) to (G), powders, surfactants, UV absorbers, humectants, colorfastness inhibitors, antioxidants, defoaming agents, beauty ingredients, preservatives, fragrances, pigments, etc., to the extent that they do not impair the effects of the present invention.
[0065] Examples of polymers other than component (B) include cross-linked methylpolysiloxanes such as (VP / hexadecene) copolymer and (dimethicone / vinyl dimethicone) crosspolymer, cross-linked methylphenylpolysiloxanes such as (dimethicone / phenyl dimethicone) crosspolymer, cross-linked alkyl-modified silicones such as (vinyl dimethicone / lauryl dimethicone) crosspolymer, cross-linked polyether-modified silicones such as dimethicone / (PEG-10 / 15)) crosspolymer, cross-linked alkyl-polyether copolymerized silicones such as (PEG-15 / lauryl dimethicone) crosspolymer, and cross-linked polyglycerin-modified silicones such as (dimethicone / polyglycerin-3) crosspolymer, and these can be used one or in combination of two or more. Among these, (VP / hexadecene) copolymer, crosslinked polyether-modified silicone, crosslinked alkyl-polyether copolymer, and crosslinked polyglycerin-modified silicone are preferred, and (VP / hexadecene) copolymer, crosslinked polyether-modified silicone, and crosslinked alkyl-polyether copolymer are more preferred. Furthermore, if two or more types are included, it is even more preferable to include (VP / hexadecene) copolymer and crosslinked methylpolysiloxane.
[0066] Commercially available products include, for example, (VP / hexadecene) copolymers such as ANTARON V216 (manufactured by ASHLAND SPECIALTYING REDIENTS), and dimethicone crosspolymers such as DOWSIL 9040 SILICONE ELASTOMER BLEND (88% volatile cyclomethicone solution), DOWSIL EL-9140 SILICONE ELASTOMER BLEND (85% volatile dimethicone solution), DOWSIL 9541 SILICONE ELASTOMER BLEND (84% volatile dimethicone solution), and DOWSIL EL-8040 ID SILICONE ORGANIC. BLEND (82% volatile isododecane solution) (manufactured by Dow-Toray), BELSIL EG1200 (86% dimethicone solution) (manufactured by Asahi Kasei Wacker Silicone Co., Ltd.), (Dimethicone / Vinyl Dimethicone) Crosspolymers: KSG-6 (40% dimethicone solution), KSG-15 (95% volatile cyclomethicone solution), KSG-16 (75% dimethicone solution), KSG-016F (75% dimethicone solution), KSG-19 (85% dimethicone solution) (manufactured by Shin-Etsu Chemical Co., Ltd.), DOWSIL EL-9080 SILICONE ELASTOMER BLEND (86% volatile cyclomethicone solution), DOWSIL EL-9081 SILICONE ELASTOMER BLEND (86% volatile dimethicone solution) (manufactured by Dow Toray), BELSIL EG7 (75% dimethicone solution) (manufactured by Asahi Kasei Wacker Silicone Co., Ltd.); KSG-18 (85% diphenylsiloxy phenyl trimethicone solution) (manufactured by Shin-Etsu Chemical Co., Ltd.) as a (dimethicone / phenylvinyl dimethicone) crosspolymer; BELSIL EG 6000 (87% dimethicone solution) (manufactured by Asahi Kasei Wacker Silicone Co., Ltd.); KSG-41A (70% mineral oil solution), KSG-42A (80% volatile isododecane solution), KSG-43 (70% triethylhexanoin solution) as (vinyl dimethicone / lauryl dimethicone) crosspolymers (all manufactured by Shin-Etsu Chemical Co., Ltd.); KSG-310 (mineral oil solution) as (PEG-15 / lauryl dimethicone) crosspolymer (manufactured by Shin-Etsu Chemical Co., Ltd.);KSG-710 (dimethicone solution) (manufactured by Shin-Etsu Chemical Co., Ltd.) as a (dimethicone / polyglycerin-3) crosspolymer; KSG-210 (dimethicone solution) (manufactured by Shin-Etsu Chemical Co., Ltd.) as a (dimethicone / (PEG-10 / 15)) crosspolymer; KSP-100 (manufactured by Shin-Etsu Chemical Co., Ltd.), KSP-101 (manufactured by Shin-Etsu Chemical Co., Ltd.), KSP- Examples include 102 (manufactured by Shin-Etsu Chemical Co., Ltd.), KSP-300 (manufactured by Shin-Etsu Chemical Co., Ltd.) as a (diphenyldimethicone / vinyldiphenyldimethicone / silsesquioxane) crosspolymer, and X-25-9148A (70% cyclopentasiloxane solution) and X-25-9148B (50% isododecane solution) (both manufactured by Shin-Etsu Chemical Co., Ltd.) as (dimethicone / vinyltrimethylsiloxysilicate) crosspolymers.
[0067] Other oily components besides components (A) to (G) include higher alcohols, fluorinated oils, and oily gelling agents, regardless of their origin (animal oils, vegetable oils, synthetic oils, etc.) or their properties (solid oils, semi-solid oils, liquid oils, etc.). Specifically, these include higher alcohols such as stearyl alcohol, cetyl alcohol, lauryl alcohol, oleyl alcohol, isostearyl alcohol, and behenyl alcohol; silicones such as decamethylcyclopentasiloxane and fluorinated organopolysiloxane; fluorinated oils such as perfluorodecane, perfluorooctane, and perfluoropolyether; and oily gelling agents such as starch fatty acid esters, 12-hydroxystearic acid, and calcium stearate.
[0068] The powder is not particularly limited in terms of shape (plate-like, spindle-like, needle-like, etc.), particle size (fine particles, pigment-grade, etc.), particle structure (porous, non-porous, etc.), etc., and examples include inorganic powders, organic powders, composite powders, etc. Specifically, examples include inorganic powders such as titanium dioxide, black titanium dioxide, ultramarine, red iron oxide, yellow iron oxide, black iron oxide, zinc oxide, aluminum oxide, anhydrous silicic acid, magnesium oxide, zirconium oxide, magnesium carbonate, calcium carbonate, chromium oxide, chromium hydroxide, carbon black, aluminum silicate, magnesium silicate, aluminum magnesium silicate, mica, synthetic mica, sericite, talc, kaolin, silicon carbide, barium sulfate, boron nitride, etc.; organic powders such as magnesium stearate, zinc stearate, N-acyllysine, cellulose, starch, silk, etc.; and composite powders such as fine-particle titanium dioxide-containing silicon dioxide and fine-particle zinc oxide-containing silicon dioxide, etc., and one or more of these can be used. Furthermore, the surface may be coated with a surface treatment agent. Specifically, the surface treatment agent may be one obtained by known methods using inorganic substances such as silica and alumina, or organic substances such as triethoxyalkylsilane, organic titanate, N-acyl amino acids, amino acids, phospholipids, silicones, metallic soaps, surfactants, oils, or hydrocarbons. One or more surface treatment agents may be used for coating.
[0069] Any surfactant commonly used in cosmetics can be used, including nonionic surfactants, anionic surfactants, cationic surfactants, and amphoteric surfactants.
[0070] Examples of UV absorbers include ethylhexyl methoxycinnamate, ethylhexyl salicylate, dimethyldiethylbenzalmalonate, diethylaminohydroxybenzoylhexyl benzoate, methylenebisbenzotriazolyltetramethylbutylphenol, 2,4-bis{[4-(2-ethylhexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine, 2,4,6-tris[4-(2-ethylhexyloxycarbonyl)anilino]-1,3,5-triazine, octocrylene, and 4-tert-butyl-4'-methoxydibenzoylmethane.
[0071] Examples of moisturizers include polyhydric alcohols, proteins, mucopolysaccharides, collagen, elastin, and keratin.
[0072] Examples of antioxidants include α-tocopherol and ascorbic acid.
[0073] Examples of beauty ingredients include vitamins, anti-inflammatory agents, and herbal medicines.
[0074] Examples of preservatives include parahydroxybenzoic acid esters, phenoxyethanol, 1,2-pentanediol, 1,2-hexanediol, 1,2-octanediol, and ethylhexylglycerin.
[0075] As for fragrances, there are no particular restrictions as long as they are fragrances commonly used in cosmetics. Examples include limonene, linalool, lavender flower extract, menthol, perillaldehyde, phenethyl alcohol, farnesol, pinene, citronellol, citral, methyl salicylate, geraniol, eugenol, and β-caryophyllene.
[0076] As for the pigments, there are no particular restrictions as long as they are pigments commonly used in cosmetics. For example, metal oxides such as titanium dioxide, zinc oxide, cerium oxide, iron oxide, titanium / titanium oxide sintered products, chromium oxide, chromium hydroxide, Prussian blue, ultramarine, etc., as well as organic pigment powders such as Red 201, Red 202, Red 205, Red 226, Red 228, Orange 203, Orange 204, Blue 404, Yellow 401, Black 401, Brown 201, Purple 401, Blue 1, Blue 2, Blue 203, Blue 205, Green 3, Green 201, Green 204, Green 20 Examples of organic dyes include zirconium, barium, or aluminum lake, such as No. 5, Green No. 401, Green No. 402, Yellow No. 4, Yellow No. 5, Yellow No. 202 (1), Yellow No. 202 (2), Yellow No. 203, Yellow No. 402, Yellow No. 403 (1), Yellow No. 406, Yellow No. 407, Orange No. 205, Orange No. 402, Red No. 2, Red No. 3, Red No. 102, Red No. 104 (1), Red No. 105 (1), Red No. 106, Red No. 227, Red No. 230 (1), Red No. 231, Red No. 401, Red No. 502, Red No. 503, Red No. 504, and Red No. 506.
[0077] The dosage form of the stick-shaped cosmetic of the present invention is not particularly limited, but oil-based cosmetics, water-in-oil cosmetics, oil-in-water cosmetics, etc. are preferred, and oil-based cosmetics are more preferred. This dosage form is more preferable from the viewpoint of maintaining the gloss of the applied film.
[0078] The stick-shaped cosmetic composition of the present invention can be used in a variety of applications, including, but is not limited to, skincare cosmetics such as whitening cosmetics, sunscreens, cleansing cosmetics such as facial cleansers and makeup removers, hair cosmetics such as shampoos, rinses, and conditioners, lip cosmetics such as lipsticks and lip glosses, makeup cosmetics such as foundations, primers, concealers, blushes, face powders, eyeliners, eye colors, eyebrow products, and nail polishes, and overcoat cosmetics. It is particularly suitable for use in lip cosmetics.
[0079] Furthermore, the present invention may also adopt the following configurations: [1] A rod-shaped cosmetic containing the following components (A) to (E): (A) wax (B) oil-soluble polyurethane (C) liquid ester oil having a viscosity of less than 3000 mPa·s at 25°C (D) liquid ester oil having a viscosity of 3000 mPa·s or more at 25°C (E) a hydrocarbon oil that is liquid at 25°C. [2] The rod-shaped cosmetic according to [1], wherein the viscosity of component (C) at 25°C is 10 mPa·s or more and less than 3000 mPa·s. [3] The rod-shaped cosmetic according to [1] or [2], wherein the viscosity of component (E) at 25°C is 10000 mPa·s or more and 1500000 mPa·s or less. [4] The rod-shaped cosmetic according to any one of [1] to [3], further containing component (F) phenyl-modified silicone. [5] A stick-shaped cosmetic according to any one of [1] to [4], further containing (G) a semi-solid ester oil at 25°C (except for component (A)). [6] A stick-shaped cosmetic according to any one of [1] to [5], which is oily. [7] A stick-shaped cosmetic according to any one of [1] to [6], which is for use on the lips.
[0080] The present invention will be described in detail below with reference to examples. However, these examples do not limit the present invention in any way.
[0081] Examples 1-18 and Comparative Examples 1-4: Stick-type oily cosmetic (lipstick) Stick-type oily cosmetic formulations were prepared according to the formulations shown in Tables 1 and 2 below, and evaluated for a. release properties from the filling mold, b. no decrease in hardness at high temperatures, c. resistance to wrinkles in the coated film, and d. gloss retention of the coated film using the evaluation methods described below. The results are also shown in Tables 1 and 2.
[0082]
[0083] *1 CIREWAX 90 (manufactured by CIREBELLE) *2 CIREWAX 80 (manufactured by CIREBELLE) *3 OILKEMIA 5S CC POLYMER (manufactured by Lubrizol) Solids content 30%, component (B) is a copolymer of hydrogenated poly(C6-20 olefin) and (HDI / trimethylol hexyllactone) crosspolymer, component (C) is tri(caprylic / capric acid) glyceryl (viscosity 23 mPa·s)
[0084] (Manufacturing Method) A. Dissolve components (1) to (14) uniformly at 100°C. B. Add components (15) to (18) to A and mix and disperse uniformly using a roll mill. C. Fill B into a rubber mold (12Φ) container while stirring at 100°C or higher. D. Cool C to -10°C and insert into a lifting container to obtain a stick-shaped oily cosmetic (lipstick).
[0085] (Evaluation Method) Each of the following evaluation items was evaluated using the method described below.
[0086] (Evaluation Items) a. Release properties from the filling mold For evaluation item a, each sample was filled into a rubber mold (12Φ) container, and the release properties from the filling mold and defects in appearance when dispensed (unevenness during filling, peeling) of the cooled and solidified stick-shaped oil lipstick were visually judged. 20 lipsticks were filled, and those with poor release properties or defects in appearance were counted as defective products and judged according to the following criteria. (Number of defective products): (Judgment) 1 or less: Excellent: AA 2 to 3: Very good: A 4 to 5: Good: B 6 to 7: Slightly poor: C 8 or more: Poor: D
[0087] (Evaluation item) b. No decrease in hardness at high temperatures For evaluation item b, each sample was filled into a rubber mold (12Φ) container, and the stick-shaped oily lipstick, after cooling and solidifying, was left at 25°C for 24 hours. This was used as the reference for the hardness value at which the stick-shaped oily lipstick was left at 25°C for 24 hours after being stored at 50°C for one month. The hardness change was judged according to the following criteria by comparing it with the hardness value at which the stick-shaped oily lipstick was left at 25°C for 24 hours after being stored at 50°C for one month. The hardness at which the hardness was at which it (Percentage of hardness reduction): (Judgment) Hardness reduction less than 15%: Excellent: AA Hardness reduction 15% to less than 20%: Very good: A Hardness reduction 20% to less than 25%: Good: B Hardness reduction 25% to less than 30%: Slightly poor: C Hardness reduction 30% or more: Poor: D
[0088] (Evaluation item) c. Invisibility of wrinkles in the coated film For evaluation item c, the condition of vertical lip wrinkles before and after application of each sample was compared to evaluate the invisibility of vertical lip wrinkles. Each sample was tested by a panel of 10 cosmetic evaluation specialists, and each panel member evaluated it on a 7-point scale according to the absolute evaluation criteria below and assigned a score. The average score was calculated from the sum of the scores of all panel members for each sample, and the evaluation was made according to the 5-point judgment criteria below. (Absolute Evaluation Criteria) (Rating): (Evaluation) 6 points: Very inconspicuous 5 points: Inconspicuous 4 points: Somewhat inconspicuous 3 points: Average 2 points: Somewhat conspicuous 1 point: Conspicuous 0 points: Very conspicuous (5-point rating criteria) (Rating): (Average score of ratings) AA: Above 5.5 points: Excellent A: Above 5 points and below 5.5 points: Very good B: Above 3.5 points and below 5 points: Good C: Above 2 points and below 3.5 points: Somewhat poor D: Below 2 points: Poor
[0089] (Evaluation Item) d. Gloss Duration of the Coating Film For evaluation item d, the gloss was evaluated by comparing the gloss immediately after application to the lips with the gloss 60 minutes later. Each sample was tested by a panel of 10 cosmetic evaluation specialists, and each panel member evaluated it on a 7-point scale according to the absolute evaluation criteria below and assigned a score. The average score was calculated from the sum of the scores from all panel members for each sample, and the result was judged according to the 5-point judgment criteria below. (Absolute Evaluation Criteria) (Score): (Evaluation) 6 points: Very well maintained 5 points: Well maintained 4 points: Somewhat maintained 3 points: Average 2 points: Somewhat poorly maintained 1 point: Poorly maintained 0 points: Very poorly maintained (5-Level Judgment Criteria) (Judgment): (Average score of scores) AA: Over 5.5 points: Excellent A: Over 5 points and 5.5 points or less: Very good B: Over 3.5 points and 5 points or less: Good C: Over 2 points and 3.5 points or less: Somewhat poor D: 2 points or less: Poor
[0090] As is clear from the results in Tables 1 and 2, the stick-shaped oil-based lipsticks of Examples 1 to 18 of the present invention provided superior quality compared to the stick-shaped oil-based lipsticks of Comparative Examples 1 to 4, achieving better gloss retention and reduced wrinkles in the coated film, while also demonstrating excellent release properties from the mold and no decrease in hardness at high temperatures. On the other hand, Comparative Example 1, which did not contain ingredient (A), was difficult to mold into a stick shape and did not meet the criteria for a cosmetic product that could be evaluated in all aspects. Comparative Example 2, which did not contain ingredient (B), was poor in terms of release properties from the mold and no decrease in hardness at high temperatures. Comparative Example 3, which did not contain ingredient (D), and Comparative Example 4, which did not contain ingredient (E), were poor in terms of reduced wrinkles in the coated film and gloss retention of the coated film.
[0091] Example 19: Stick-type lipstick (oil-based cosmetic) (Ingredients) (%) 1: Ethylene / propylene copolymer*4 5.0 2: Microcrystalline wax*5 2.0 3: Carnauba wax*6 2.0 4: Tri(caprylic / capric acid) glyceryl (viscosity 23 mPa·s) hydrogenated poly(C6-20 olefin) (HDI / trimethylol hexyllactone) crosspolymer*3 0.5 5: Polyglyceryl-2 triisostearate*7 (viscosity 350-450 mPa·s <center value 400 mPa·s>) remaining amount 6: Diisostearyl malate*8 (viscosity 2700 mPa·s) 10.0 7: Polybutene*9 (viscosity 1,000,000 mPa·s) 10.0 8: Diphenylsiloxyphenyl trimethicone *10 10.0 9: Dimer dilinoleate (phytosteryl / isostearyl / cetyl / stearyl / behenyl) *11 10.0 10: Hydrogenated rosin condensate of dimer dilinoleyl *12 (viscosity 33000 mPa·s) 5.0 11: Petrolatum 5.0 12: Sericite 3.0 13: Anhydrous silicic acid *13 1.0 14: Calcium carbonate 0.1 15: 2,6-Di-tert-butyl-para-cresol 0.1 16: Phenoxyethanol 0.1 17: Sodium benzoate 0.1 18: Tocopheryl acetate 0.1 19: 1% dilauroyl glutamate lysine sodium treated titanium dioxide 1.5 20: 5% dimethylpolysiloxane treated black iron oxide 0.1 21: Red No. 202 0.5 22: Yellow No. 4 0.5 23: Titanium mica*14 5.0 24: Zinc oxide 1.0 25: Fragrance 0.1 *4 EP-700 (manufactured by Baker Petrolite) *5 Multiwax W-445 (manufactured by SONNEBORN) *6 Refined carnauba wax No. 1 (manufactured by Nippon Natural Products Co., Ltd.) *7 Cosmol 43V (manufactured by Nisshin Oillio Group Co., Ltd.) *8 High Malate DIS (manufactured by Higher Alcohol Industry Co., Ltd.) *9 Nippon Oil Polybutene HV-1900 (manufactured by ENEOS Corporation) *10 KF-56 (manufactured by Shin-Etsu Chemical Co., Ltd.) *11 PLANDOOL-S (manufactured by Nippon Seika Co., Ltd.) *12 LUSPLAN DD-DHR (manufactured by Nippon Seika Co., Ltd.) *13 AEROSIL 380S (manufactured by Nippon Aerosil Co., Ltd.) *14 TIMICA EXTRA BRIGHT 1500 (manufactured by BASF Corporation)
[0092] (Manufacturing Method) A: Dissolve components (1) to (11) uniformly at 100 to 110°C. B: Add components (12) to (25) to A and mix and disperse uniformly. C: After degassing B, heat and pour into a lipstick mold. After cooling, remove from the mold and load into a container to obtain a stick-type lipstick. The stick-type lipstick of Example 19 provided excellent quality in terms of gloss retention of the coated film, inconspicuousness of wrinkles in the coated film, release from the filling mold, and no decrease in hardness at high temperatures.
[0093] Example 20: Stick-type lip balm (water-in-oil cosmetic) (Ingredients) (%) 1: Synthetic wax*1 5.0 2: Microcrystalline wax*5 2.0 3: Carnauba wax*6 2.0 4: Tri(caprylic / capric acid) glyceryl (viscosity 23 mPa·s) hydrogenated poly(C6-20 olefin) (HDI / trimethylol hexyllactone) crosspolymer*3 0.5 5: Triethylhexanoin*15 (viscosity 20-30 mPa·s <center value 25 mPa·s>) 10.0 6: Triisostearin*16 (viscosity 12000-14000 mPa·s <center value 13000 mPa·s>) 5.0 7: Polybutene*17 (viscosity 37000 mPa·s) 5.0 8: Diphenyl dimethicone*18 5.0 9: Lauroyl glutamate di(octyldodecyl / phytosteryl / behenyl)*12 1.0 10: Lauryl polyglyceryl-3-polydimethylsiloxyethyl dimethicone*19 3.0 11: Diphenylsiloxy phenyl trimethicone*20 4.25 12: (Dimethicone / phenyl vinyl dimethicone) crosspolymer*20 0.75 13;Dimethicone*21 1.0 14: Purified water remaining 15: BG 10.0 16: Scutellaria baicalensis extract 0.05 17: Avocado extract 0.05 18: Aloe vera leaf extract 0.05 19: Grapefruit fruit extract 0.05 20: Phenoxyethanol 0.1 21: EDTA salt 0.05 22: Red iron oxide 0.3 23: Fragrance 0.1 *15 MYRITOL GTEH (manufactured by BASF) *16 Saracos 3318 (manufactured by Nisshin Oillio Group) *17 Purified polybutene HV-100F (SB) (manufactured by Nippon Natural Products Co., Ltd.) *18 KF-54 (manufactured by Shin-Etsu Chemical Co., Ltd.) *19 KF-6105 (manufactured by Shin-Etsu Chemical Co., Ltd.) *20 Silicone KSG-18 (manufactured by Shin-Etsu Chemical Co., Ltd.) *21 Silicone KF-96A (6CS) (manufactured by Shin-Etsu Chemical Co., Ltd.);
[0094] (Manufacturing Method) A: Dissolve components (1) to (13) uniformly at 100 to 110°C. B: Add component (22) to A and mix and disperse uniformly at 70 to 80°C. C: Dissolve components (14) to (21) and (23) uniformly at 70 to 80°C. D: Add C to B and emulsify. E: After degassing D, heat and pour into a lipstick mold. After cooling, remove from the mold and load into a container to obtain a stick-type lip balm. The stick-type lip balm of Example 20 provided excellent quality in terms of gloss retention of the applied film, reduced visibility of wrinkles in the applied film, release from the filling mold, and no decrease in hardness at high temperatures.
Claims
1. A bar-shaped cosmetic containing the following components (A) to (E): (A) wax, (B) oil-soluble polyurethane, (C) liquid ester oil with a viscosity of less than 3000 mPa·s at 25°C, (D) liquid ester oil with a viscosity of 3000 mPa·s or more at 25°C, and (E) a hydrocarbon oil that is liquid at 25°C.
2. The rod-shaped cosmetic composition according to claim 1, wherein the viscosity of component (C) at 25°C is 10 mPa·s or more and less than 3000 mPa·s.
3. The rod-shaped cosmetic composition according to claim 1 or 2, wherein the viscosity of component (E) at 25°C is 10,000 mPa·s or more and 1,500,000 mPa·s or less.
4. The rod-shaped cosmetic composition according to claim 1 or 2, further comprising component (F) phenyl-modified silicone.
5. The rod-shaped cosmetic composition according to claim 1 or 2, further comprising component (G) a semi-solid ester oil at 25°C (excluding component (A)).
6. The stick-shaped cosmetic composition according to claim 1 or 2, which is oil-based.
7. A stick-shaped cosmetic composition for use on the lips, as described in claim 1 or 2.
Citation Information
Patent Citations
Improved Anti-transferring cosmetics composition
JP1994199630A
Oil-based cosmetic for preventing secondary adhesion
JP2020033339A
High Shine, Stick-Shaped Cosmetic Products
US20110171152A1
Lip cosmetic
WO2017216981A1
Polyurethane gel composition and use thereof
WO2018181899A1