JP2005314358A - Make up remover composition - Google Patents
Make up remover composition Download PDFInfo
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- JP2005314358A JP2005314358A JP2005038502A JP2005038502A JP2005314358A JP 2005314358 A JP2005314358 A JP 2005314358A JP 2005038502 A JP2005038502 A JP 2005038502A JP 2005038502 A JP2005038502 A JP 2005038502A JP 2005314358 A JP2005314358 A JP 2005314358A
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- component
- remover composition
- makeup
- makeup remover
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- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 61
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 39
- 125000003709 fluoroalkyl group Chemical group 0.000 claims abstract description 23
- 239000007788 liquid Substances 0.000 claims abstract description 15
- 238000004132 cross linking Methods 0.000 claims abstract description 11
- 150000002430 hydrocarbons Chemical group 0.000 claims description 13
- 239000003960 organic solvent Substances 0.000 claims description 13
- 229920006136 organohydrogenpolysiloxane Polymers 0.000 claims description 8
- BANXPJUEBPWEOT-UHFFFAOYSA-N 2-methyl-Pentadecane Chemical compound CCCCCCCCCCCCCC(C)C BANXPJUEBPWEOT-UHFFFAOYSA-N 0.000 claims description 6
- LEEDMQGKBNGPDN-UHFFFAOYSA-N 2-methylnonadecane Chemical compound CCCCCCCCCCCCCCCCCC(C)C LEEDMQGKBNGPDN-UHFFFAOYSA-N 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 6
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- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- SCRSFLUHMDMRFP-UHFFFAOYSA-N trimethyl-(methyl-octyl-trimethylsilyloxysilyl)oxysilane Chemical compound CCCCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C SCRSFLUHMDMRFP-UHFFFAOYSA-N 0.000 claims description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 5
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 claims description 4
- FBZANXDWQAVSTQ-UHFFFAOYSA-N dodecamethylpentasiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C FBZANXDWQAVSTQ-UHFFFAOYSA-N 0.000 claims description 4
- 229940087203 dodecamethylpentasiloxane Drugs 0.000 claims description 4
- 229940043268 2,2,4,4,6,8,8-heptamethylnonane Drugs 0.000 claims description 3
- GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 claims description 3
- IUMSDRXLFWAGNT-UHFFFAOYSA-N Dodecamethylcyclohexasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 IUMSDRXLFWAGNT-UHFFFAOYSA-N 0.000 claims description 3
- SGVYKUFIHHTIFL-UHFFFAOYSA-N Isobutylhexyl Natural products CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 claims description 3
- YFCGDEUVHLPRCZ-UHFFFAOYSA-N [dimethyl(trimethylsilyloxy)silyl]oxy-dimethyl-trimethylsilyloxysilane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C YFCGDEUVHLPRCZ-UHFFFAOYSA-N 0.000 claims description 3
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- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 claims description 3
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- 230000000052 comparative effect Effects 0.000 description 6
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 5
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- 230000000694 effects Effects 0.000 description 4
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- 239000002904 solvent Substances 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
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- 229940058015 1,3-butylene glycol Drugs 0.000 description 3
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- 238000004898 kneading Methods 0.000 description 3
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- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- QBQHVWBLUJBPHT-UHFFFAOYSA-N 2-(3,3,3-trifluoropropyl)-1,3,5,7,9,2,4,6,8,10-pentaoxapentasilecane Chemical compound FC(F)(F)CC[SiH]1O[SiH2]O[SiH2]O[SiH2]O[SiH2]O1 QBQHVWBLUJBPHT-UHFFFAOYSA-N 0.000 description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
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- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 150000003284 rhodium compounds Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- RSNQKPMXXVDJFG-UHFFFAOYSA-N tetrasiloxane Chemical compound [SiH3]O[SiH2]O[SiH2]O[SiH3] RSNQKPMXXVDJFG-UHFFFAOYSA-N 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
Landscapes
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
本発明は、メイクアップリムーバー組成物に関するものであり、更に詳しくは、特定の三次元架橋構造を有するシリコーン重合物とフルオロアルキル基含有オルガノポリシロキサンを含有し、耐水性、耐油性が高く落としにくいメイクアップ化粧料も、スムーズに除去することが可能なメイクアップリムーバー組成物に関するものである。 The present invention relates to a makeup remover composition, and more specifically, it contains a silicone polymer having a specific three-dimensional cross-linked structure and a fluoroalkyl group-containing organopolysiloxane, and has high water resistance and oil resistance and is difficult to drop. Makeup cosmetics also relate to a makeup remover composition that can be removed smoothly.
メイクアップ化粧料は、化粧持ちを向上させるために様々な機能性素材が応用されている。具体的には耐水性の高いシリコーン化合物が粉体の表面処理剤や或いは油剤の一部として配合されたり、また更には、耐油性の高いフッ素化合物が効果的に配合されているメイクアップ化粧料も多い。一方、洗浄剤として一般に用いられているエチレンオキサイド付加ポリプロピレングリコール系界面活性剤やイミダゾリニウムベタイン等で構成されるクレンジング料では、ふき取り時にメイクアップ化粧料が周囲ににじむように広がってしまうなどの使用性が悪く、また、特に化粧持ちの高いメイクアップ化粧料においては、メイクアップ化粧料自体の落ちが悪いなどの問題があった。そこで、下記文献(特許文献1〜6参照)に示すように脂肪酸モノエタノールアマイド系界面活性剤や、ジアルキルリン酸塩、エチレンオキサイド付加ポリプロピレングリコール系界面活性剤などの界面活性剤と、油分やシリコーン油を併せて配合することでメイクアップ化粧料の落ち(以下、単に「メイク落ち」と記す場合がある)と使用性の改良が図られているが、特に撥水、撥油性の高いフッ素化合物が配合された耐水性、耐油性が高い化粧料に関しては、メイク落ちや使用性に関して必ずしも満足の行くものではなかった。 Various functional materials are applied to make-up cosmetics in order to improve the longevity of makeup. Specifically, makeup cosmetics in which a silicone compound having high water resistance is blended as a part of a powder surface treatment agent or oil, or a fluorine compound having high oil resistance is blended effectively. There are also many. On the other hand, cleansing compositions composed of ethylene oxide-added polypropylene glycol surfactants and imidazolinium betaines, which are commonly used as cleaning agents, spread the makeup cosmetics to spread around when wiped off. There is a problem in that the usability is poor, and especially in the makeup cosmetics with a long makeup, the makeup cosmetics themselves are poorly dropped. Therefore, as shown in the following documents (see Patent Documents 1 to 6), surfactants such as fatty acid monoethanolamide surfactants, dialkyl phosphates, ethylene oxide-added polypropylene glycol surfactants, oils and silicones The combination of oil has been used to improve make-up cosmetics (hereinafter sometimes referred to simply as “make-up removal”) and improved usability, but it is a fluorine compound with particularly high water and oil repellency. In regard to cosmetics with high water resistance and oil resistance blended with, the makeup removal and usability were not always satisfactory.
従って、本発明の課題は、耐水性、耐油性が高く、化粧持ちの高いメイクアップ化粧料、例えば、フッ素化合物が含有されているメイクアップ化粧料に対してもメイク落ちが良く、且つ、使用性、使用感も良好なメイクアップリムーバー組成物を提供することにある。 Accordingly, the object of the present invention is to provide good makeup removal and use even for makeup cosmetics having high water resistance and oil resistance and having a long makeup, for example, makeup cosmetics containing a fluorine compound. An object of the present invention is to provide a makeup remover composition having good properties and usability.
本発明者らは上記の問題に鑑み、鋭意研究を重ねた結果、特定の三次元架橋構造を有するシリコーン重合物とフルオロアルキル基含有オルガノポリシロキサンを含有するメイクアップリムーバー組成物が、適度な粘度を有し使用性に優れ、耐水性、耐油性の高い落としにくいメイクアップ化粧料との親和性が高く、スムーズにメイクアップ化粧料を除去することができることを見出した。更に、揮発性液状油を併用することで、油性感やべたつきがより軽減された優れたメイクアップリムーバー組成物が得られることを見出し本発明の完成に至った。 In view of the above problems, the present inventors have conducted extensive research, and as a result, a makeup remover composition containing a silicone polymer having a specific three-dimensional crosslinked structure and a fluoroalkyl group-containing organopolysiloxane has an appropriate viscosity. It has been found that it has excellent usability, has high water resistance and oil resistance, and has high affinity with makeup cosmetics that are difficult to be removed, and can be removed smoothly. Furthermore, it has been found that by using a volatile liquid oil in combination, an excellent makeup remover composition with reduced oiliness and stickiness can be obtained, and the present invention has been completed.
すなわち、本発明は次の成分(A)〜(B):
(A)下記一般式(1)で示されるオルガノハイドロジェンポリシロキサン
R1 aHbSiO(4−a−b)/2 (1)
と、下記一般式(2)で示されるオルガノポリシロキサン
R1 cR2 dSiO(4−c−d)/2 (2)
を重合してなり、有機溶剤に不溶で、かつ自重と同質量以上のペンタ−3,3,3−トリフロロプロピルペンタメチルシクロペンタシロキサンを含みうることを特徴とする三次元架橋構造を有するシリコーン重合物〔但し、式中R1はそれぞれ同じか又は異なってもよく、脂肪族不飽和結合を有しない、置換又は非置換の、炭素数1〜20の一価炭化水素基であって、その11〜60モル%がフッ素置換一価炭化水素基である一価炭化水素基であり、R2は末端ビニル基を有する炭素数2〜10の一価炭化水素基であり、aは1.0から2.3、bは0.001〜1.0、cは1.0〜2.3、dは0.001〜1.0であって、1.5≦a+b≦2.6、1.5≦c+d≦2.6を満たす。〕
(B)フルオロアルキル基含有オルガノポリシロキサン
を含有するメイクアップリムーバー組成物に関するものである。また、成分(B)が、前記一般式(3)で表されるフルオロアルキル基含有オルガノポリシロキサンであるメイクアップリムーバー組成物に関するものである。また更に、成分(C)揮発性液状油を含有するメイクアップリムーバー組成物に関するものであり、更に、成分(C)がイソヘキサデカン、イソドデカン及びそれらの混合物から選択される軽質流動イソパラフィン、オクタメチルシクロテトラシロキサン、デカメチルシクロペンタシロキサン及びドデカメチルシクロヘキサシロキサンから選択される環状ジメチルポリシロキサン、オクタメチルトリシロキサン、デカメチルテトラシロキサン、ドデカメチルペンタシロキサン、ヘプタメチルオクチルトリシロキサンから選択されるオルガノポリシロキサンの一種又は二種以上であるメイクアップリムーバー組成物に関するものである。
That is, the present invention includes the following components (A) to (B):
(A) Organohydrogenpolysiloxane represented by the following general formula (1) R 1 a H b SiO (4-ab) / 2 (1)
And organopolysiloxane R 1 c R 2 d SiO (4-cd) / 2 (2) represented by the following general formula (2):
A silicone having a three-dimensional cross-linking structure, characterized in that it can contain penta-3,3,3-trifluoropropylpentamethylcyclopentasiloxane that is insoluble in an organic solvent and has the same mass or more as its own weight. Polymers wherein R 1 may be the same or different and each is a substituted or unsubstituted monovalent hydrocarbon group having 1 to 20 carbon atoms and having no aliphatic unsaturated bond, 11 to 60 mol% is a monovalent hydrocarbon group which is a fluorine-substituted monovalent hydrocarbon group, R 2 is a monovalent hydrocarbon group having 2 to 10 carbon atoms having a terminal vinyl group, and a is 1.0 2.3, b is 0.001 to 1.0, c is 1.0 to 2.3, d is 0.001 to 1.0, and 1.5 ≦ a + b ≦ 2.6. 5 ≦ c + d ≦ 2.6 is satisfied. ]
(B) The present invention relates to a makeup remover composition containing a fluoroalkyl group-containing organopolysiloxane. Moreover, the component (B) relates to a makeup remover composition that is a fluoroalkyl group-containing organopolysiloxane represented by the general formula (3). Furthermore, the present invention relates to a makeup remover composition containing component (C) volatile liquid oil, and further, light liquid isoparaffin, octamethylcyclohexane, wherein component (C) is selected from isohexadecane, isododecane and mixtures thereof. Organopolysiloxane selected from cyclic dimethylpolysiloxane selected from tetrasiloxane, decamethylcyclopentasiloxane and dodecamethylcyclohexasiloxane, octamethyltrisiloxane, decamethyltetrasiloxane, dodecamethylpentasiloxane, heptamethyloctyltrisiloxane It is related with the makeup remover composition which is 1 type, or 2 or more types.
本発明のメイクアップリムーバー組成物は、耐水性、耐油性の高い落としにくいメイクアップ化粧料との親和性が高く、スムーズにメイクアップ化粧料を除去することができ、また、手へのとりやすさ、油性感、べたつきが軽減されるなどの使用性、使用感も良好なものである。 The makeup remover composition of the present invention has a high affinity with a makeup cosmetic that is highly resistant to water and oil, and can be removed smoothly, and is easy to take on the hand. It also has good usability and usability, such as reduced oiliness and stickiness.
以下、本発明について詳細に説明する。
本発明で用いられる成分(A)の特定のシリコーン重合物は、耐水性、耐油性の高いメイクアップ化粧料となじみは良いが化粧料に使用される一般的な油剤との親和性が乏しいため化粧料へ安定に配合しにくい成分(B)のフルオロアルキル基含有オルガノポリシロキサンをメイクアップ化粧料へ安定に配合するために、また、成分(B)を含有する化粧料の製造を容易にするために用いられるものであり、また更には、肌へ塗布したときののび広がりのコントロール、油性感やべたつき感を抑えるなどの使用感の向上を目的して用いられるものである。成分(A)は、下記一般式(1)で示されるオルガノハイドロジェンポリシロキサン
R1 aHbSiO(4−a−b)/2 (1)
と、下記一般式(2)で示されるオルガノポリシロキサン
R1 cR2 dSiO(4−c−d)/2 (2)
を重合してなり、有機溶剤に不溶で、かつ自重と同質量以上のペンタ−3,3,3−トリフルオロプロピルペンタメチルシクロペンタシロキサンを含みうることを特徴とする三次元架橋構造を有するシリコーン重合物を示す。〔但し、式中R1はそれぞれ同じか又は異なってもよく、脂肪族不飽和結合を有しない、置換又は非置換の、炭素数1〜20の一価炭化水素基であって、その11〜60モル%がフッ素置換一価炭化水素基である一価炭化水素基であり、R2は末端ビニル基を有する炭素数2〜10の一価炭化水素基であり、aは1.0から2.3、bは0.001〜1.0、cは1.0〜2.3、dは0.001〜1.0であって、1.5≦a+b≦2.6、1.5≦c+d≦2.6を満たす。〕
R1としては具体的には、メチル基、エチル基、プロピル基、ブチル基、ペンチル基、ヘキシル基、ヘプチル基、オクチル基、ノニル基、デシル基等のアルキル基、シクロペンチル基、シクロヘキシル基等の飽和脂環式炭化水素基、フェニル基、トリル基等のアリール基、トリフルオロプロピル基、ノナフルオロヘキシル基、ヘプタデシルフルオロデシル基等のフッ素置換アルキル基等を挙げることができるが、特にメチル基及びトリフルオロプロピル基が好ましい。
Hereinafter, the present invention will be described in detail.
The specific silicone polymer of component (A) used in the present invention is compatible with makeup cosmetics with high water resistance and oil resistance, but has a poor affinity with general oils used in cosmetics. In order to stably blend the fluoroalkyl group-containing organopolysiloxane of component (B), which is difficult to be stably blended into cosmetics, into makeup cosmetics, and to facilitate the production of cosmetics containing component (B) Further, it is used for the purpose of improving the feeling of use, such as controlling the spread of spread when applied to the skin, and suppressing the oiliness and stickiness. Component (A) is an organohydrogenpolysiloxane represented by the following general formula (1) R 1 a H b SiO (4-ab) / 2 (1)
And organopolysiloxane R 1 c R 2 d SiO (4-cd) / 2 (2) represented by the following general formula (2):
A silicone having a three-dimensional crosslinked structure, characterized in that it can contain penta-3,3,3-trifluoropropylpentamethylcyclopentasiloxane that is insoluble in an organic solvent and has the same mass or more as its own weight. A polymer is shown. [In the formula, R 1 may be the same or different and each represents a substituted or unsubstituted monovalent hydrocarbon group having 1 to 20 carbon atoms and having no aliphatic unsaturated bond, 60 mol% is a monovalent hydrocarbon group which is a fluorine-substituted monovalent hydrocarbon group, R 2 is a monovalent hydrocarbon group having 2 to 10 carbon atoms having a terminal vinyl group, and a is from 1.0 to 2 .3, b is 0.001 to 1.0, c is 1.0 to 2.3, d is 0.001 to 1.0, and 1.5 ≦ a + b ≦ 2.6, 1.5 ≦ c + d ≦ 2.6 is satisfied. ]
Specific examples of R 1 include methyl groups, ethyl groups, propyl groups, butyl groups, pentyl groups, hexyl groups, heptyl groups, octyl groups, nonyl groups, decyl groups and other alkyl groups, cyclopentyl groups, cyclohexyl groups, and the like. Examples thereof include aryl groups such as saturated alicyclic hydrocarbon groups, phenyl groups, and tolyl groups, fluorine-substituted alkyl groups such as trifluoropropyl groups, nonafluorohexyl groups, and heptadecylfluorodecyl groups. And trifluoropropyl groups are preferred.
有機基R1のうち、11〜60モル%がフッ素置換1価炭化水素基であることが必須である。11モル%未満であると(B)成分のフルオロアルキル基含有オルガノポリシロキサンへの親和性が乏しくなり、60モル%を超えると一般式(1)で示されるオルガノハイドロジェンポリシロキサンの製造が困難になる。好ましい範囲としては、20〜50モル%である。 It is essential that 11 to 60 mol% of the organic group R 1 is a fluorine-substituted monovalent hydrocarbon group. If it is less than 11 mol%, the affinity of the component (B) for the fluoroalkyl group-containing organopolysiloxane becomes poor, and if it exceeds 60 mol%, it is difficult to produce the organohydrogenpolysiloxane represented by the general formula (1). become. A preferred range is 20 to 50 mol%.
R2としては具体的には、ビニル基、アリル基、ブテニル基、ペンテニル基、ヘキセニル基、ヘプテニル基、オクテニル基、ノネニル基、デセニル基等を挙げられるが、特にビニル基、アリル基が望ましい。 Specific examples of R 2 include a vinyl group, an allyl group, a butenyl group, a pentenyl group, a hexenyl group, a heptenyl group, an octenyl group, a nonenyl group, and a decenyl group, and a vinyl group and an allyl group are particularly desirable.
aは1.0〜2.3を示し、aが1.0より小さいと架橋度が高くなりすぎるため自重と同質量以上のペンタ−3,3,3−トリフルオロプロピルペンタメチルシクロペンタシロキサンを含み得ず、2.3より大きいと架橋度が低くなりすぎるため、三次元架橋構造の形成が困難になる。より好ましい範囲としては1.2〜2.1である。 a represents 1.0 to 2.3, and when a is smaller than 1.0, the degree of crosslinking becomes too high, and therefore penta-3,3,3-trifluoropropylpentamethylcyclopentasiloxane having the same mass or more as its own weight is required. If it is not greater than 2.3, the degree of crosslinking is too low, and it is difficult to form a three-dimensional crosslinked structure. A more preferable range is 1.2 to 2.1.
bは0.001〜1.0を示し、bが0.001より小さいと架橋度が低くなりすぎるため、三次元架橋構造の形成が困難になり、1.0を超えると架橋度が高くなりすぎるため、同様に自重と同質量以上のペンタ−3,3,3−トリフルオロプロピルペンタメチルシクロペンタシロキサンを含み得なくなる。より好ましい範囲としては0.005〜0.5である。 b is 0.001 to 1.0, and if b is less than 0.001, the degree of crosslinking becomes too low, so that it is difficult to form a three-dimensional crosslinked structure, and if it exceeds 1.0, the degree of crosslinking increases. Therefore, it cannot contain penta-3,3,3-trifluoropropylpentamethylcyclopentasiloxane having the same mass or more as its own weight. A more preferable range is 0.005 to 0.5.
cは1.0〜2.3を示し、cが1.0より小さいと架橋度が高くなりすぎるため自重と同質量以上のペンタ−3,3,3−トリフルオロプロピルペンタメチルシクロペンタシロキサンを含み得ず、2.3より大きいと架橋度が低くなりすぎるため、三次元架橋構造の形成が困難になる。より好ましい範囲としては1.2〜2.1である。 c represents 1.0 to 2.3, and when c is smaller than 1.0, the degree of crosslinking becomes too high, so that penta-3,3,3-trifluoropropylpentamethylcyclopentasiloxane having the same mass or more as its own weight is added. If it is greater than 2.3, the degree of cross-linking is too low, making it difficult to form a three-dimensional cross-linked structure. A more preferable range is 1.2 to 2.1.
dは0.001〜1.0を示し、dが0.001より小さいと架橋度が低くなりすぎるため、三次元架橋構造の形成が困難になり、1.0を超えると架橋度が高くなりすぎるため、同様に自重と同質量以上のペンタ−3,3,3−トリフルオロプロピルペンタメチルシクロペンタシロキサンを含み得なくなる。より好ましい範囲としては0.005〜0.5である。 d is 0.001 to 1.0. If d is less than 0.001, the degree of crosslinking is too low, so that it is difficult to form a three-dimensional crosslinked structure. If d exceeds 1.0, the degree of crosslinking is increased. Therefore, it cannot contain penta-3,3,3-trifluoropropylpentamethylcyclopentasiloxane having the same mass or more as its own weight. A more preferable range is 0.005 to 0.5.
一般式(1)で示されるオルガノハイドロジェンポリシロキサン、及び一般式(2)で示されるオルガノポリシロキサンは直鎖状、分岐状、環状のいずれであっても良いが、重合反応を円滑に進めるためには直鎖状であること、ないしは主として直鎖状であり、一部分岐単位を含有するものが好ましい。 The organohydrogenpolysiloxane represented by the general formula (1) and the organopolysiloxane represented by the general formula (2) may be linear, branched or cyclic, but the polymerization reaction proceeds smoothly. For this purpose, it is preferably linear or mainly linear and partially containing branched units.
本発明で用いられる成分(A)の特定のシリコーン重合物を得るには、一般式(1)で示されるオルガノハイドロジェンポリシロキサン、及び一般式(2)で示されるオルガノポリシロキサンを、白金化合物(例えば、塩化白金酸、アルコール変性塩化白金酸、塩化白金酸−ビニルシロキサン錯体等)、又はロジウム化合物の存在下、室温又は加温下(約50℃〜120℃)で反応させればよい。反応を行う際には無溶媒で行ってもよいし、必要に応じて有機溶媒を使用してもよい。有機溶媒としては具体的には、メタノール、エタノール、2−プロパノール、ブタノール等の脂肪族アルコール、ベンゼン、トルエン、キシレン等の芳香族炭化水素、n−ペンタン、n−ヘキサン、シクロヘキサン等の脂肪族又は脂環式炭化水素、ジクロロメタン、クロロホルム、四塩化炭素等のハロゲン化炭化水素、アセトン、メチルエチルケトン等のケトン系溶剤等が挙げられる。しかしながら、化粧品用途として用いるためには、無溶媒、若しくはエタノール、2−プロパノールが好ましい。 In order to obtain the specific silicone polymer of the component (A) used in the present invention, an organohydrogenpolysiloxane represented by the general formula (1) and an organopolysiloxane represented by the general formula (2) (For example, chloroplatinic acid, alcohol-modified chloroplatinic acid, chloroplatinic acid-vinylsiloxane complex, etc.) or a rhodium compound may be reacted at room temperature or under heating (about 50 ° C. to 120 ° C.). When carrying out the reaction, it may be carried out without a solvent, or an organic solvent may be used if necessary. Specific examples of the organic solvent include aliphatic alcohols such as methanol, ethanol, 2-propanol and butanol, aromatic hydrocarbons such as benzene, toluene and xylene, aliphatics such as n-pentane, n-hexane and cyclohexane or Examples thereof include alicyclic hydrocarbons, halogenated hydrocarbons such as dichloromethane, chloroform and carbon tetrachloride, and ketone solvents such as acetone and methyl ethyl ketone. However, for use as a cosmetic application, no solvent, ethanol, or 2-propanol is preferable.
成分(A)の特定のシリコーン重合物は、三次元架橋構造を有し、有機溶媒に不溶なものである。ここで言う有機溶媒とは、直鎖状あるいは分岐状のペンタン、ヘキサン、ドデカン、ヘキサデカン、オクタデカン等の脂肪族系有機溶媒、ベンゼン、トルエン、キシレン等の芳香族系有機溶媒、メタノール、エタノール、プロパノール、ブタノール、ヘキサノール、デカノール等のアルコール系有機溶媒、クロロホルム、四塩化炭素等のハロゲン化有機溶媒、アセトン、メチルエチルケトン等のケトン系有機溶媒等の各種有機溶媒の他、低粘度のジメチルポリシロキサン、メチルフェニルポリシロキサン、環状ジメチルポリシロキサン等のシリコーン系化合物等が挙げられる。また、本発明に使用される成分(A)の特定のシリコーン重合物は自重と同質量以上のペンタ−3,3,3−トリフルオロプロピルペンタメチルシクロペンタシロキサンを含みうることを特徴とする。 The specific silicone polymer of component (A) has a three-dimensional crosslinked structure and is insoluble in organic solvents. The organic solvent mentioned here is an aliphatic organic solvent such as linear or branched pentane, hexane, dodecane, hexadecane or octadecane, an aromatic organic solvent such as benzene, toluene or xylene, methanol, ethanol or propanol. In addition to various organic solvents such as alcohol organic solvents such as butanol, hexanol and decanol, halogenated organic solvents such as chloroform and carbon tetrachloride, ketone organic solvents such as acetone and methyl ethyl ketone, low viscosity dimethylpolysiloxane, methyl Examples thereof include silicone compounds such as phenyl polysiloxane and cyclic dimethyl polysiloxane. In addition, the specific silicone polymer of component (A) used in the present invention is characterized in that it may contain penta-3,3,3-trifluoropropylpentamethylcyclopentasiloxane having the same mass or more as its own weight.
成分(A)の特定のシリコーン重合物は、目的に応じてその一種又は二種以上を用いることができ、その配合量は特に限定されないが、メイクアップリムーバー組成物中に0.01〜40質量%(以下、「%」と記す)が好ましく、0.1〜30%がより好ましい。この範囲であれば、成分(B)を含有するメイクアップリムーバーの製造が容易であり、且つ安定に配合できると共に、伸び広がりのコントロールや、油性感、べたつきの抑制などの使用感に優れたメイクアップリムーバー組成物が得られるため好ましい。 The specific silicone polymer of component (A) can be used singly or in combination of two or more depending on the purpose, and the blending amount is not particularly limited, but is 0.01 to 40 mass in the makeup remover composition. % (Hereinafter referred to as “%”) is preferable, and 0.1 to 30% is more preferable. Within this range, the makeup remover containing the component (B) can be easily manufactured and can be stably blended, and the makeup has excellent usability such as control of spread and spread, suppression of oiliness and stickiness. This is preferable because an up remover composition can be obtained.
本発明で用いられる成分(B)のフルオロアルキル基含有オルガノポリシロキサンは、前述のように耐水性、耐油性の高いメイクアップ化粧料とのなじみが良いことから、メイク落し効果の向上のため用いられる。成分(B)のフルオロアルキル基含有オルガノポリシロキサンは、有機基として分子中に少なくとも一つ以上のフルオロアルキル基を有するオルガノポリシロキサンである。フルオロアルキル基として具体的には、トリフルオロプロピル基、ノナフルオロヘキシル基、ヘプタデシルフルオロデシル基等のフッ素置換アルキル基が挙げられ、特にトリフルオロプロピル基が好ましい。 The fluoroalkyl group-containing organopolysiloxane of component (B) used in the present invention is used to improve the makeup removal effect because it is well-suited to makeup cosmetics with high water resistance and oil resistance as described above. It is done. The component (B) fluoroalkyl group-containing organopolysiloxane is an organopolysiloxane having at least one fluoroalkyl group in the molecule as an organic group. Specific examples of the fluoroalkyl group include fluorine-substituted alkyl groups such as a trifluoropropyl group, a nonafluorohexyl group, and a heptadecylfluorodecyl group, with a trifluoropropyl group being particularly preferred.
成分(B)のフルオロアルキル基含有オルガノポリシロキサンは、25℃における粘度が200mm2/s以下のフルオロアルキル基含有オルガノポリシロキサンが好ましく、特に好ましいのは20〜180mm2/sである。この範囲であれば、成分(A)の特定のシリコーン重合物との親和性において良好なものが得られると共に、肌に付着しているメイクアップ化粧料とのなじみが一段と良好となり、更なるメイク落ちの向上が得られることから好ましい。 The fluoroalkyl group-containing organopolysiloxane of the component (B) is preferably a fluoroalkyl group-containing organopolysiloxane having a viscosity at 25 ° C. of 200 mm 2 / s or less, particularly preferably 20 to 180 mm 2 / s. If it is this range, while being good in affinity with the specific silicone polymer of a component (A), while being familiar with the makeup cosmetics adhering to skin, it will become much better, and further makeup It is preferable because improvement in dropping is obtained.
成分(B)のフルオロアルキル基含有オルガノポリシロキサンは、直鎖状、分岐状、環状のいずれであっても良いが、粘度や成分(A)の特定のシリコーン重合物との親和性から、一般式(3)で示されるフルオロアルキル基含有オルガノポリシロキサンが特に好ましい。 The fluoroalkyl group-containing organopolysiloxane of component (B) may be linear, branched or cyclic, but in general, from the viscosity and affinity with the specific silicone polymer of component (A) A fluoroalkyl group-containing organopolysiloxane represented by the formula (3) is particularly preferred.
具体的には、直鎖状のものとして、FL−100、X−22−819、X−22−820、X−22−821、X−22−822(信越化学工業社製)、FS−1265(東レ・ダウコーニング社製)が挙げられる。環状のものとしては、特開平09−268110号公報に記載されているものが挙げられ、例えばINCI名(International Nomenclature Cosmetic Ingredient labeling names)でトリフルオロプロピルシクロテトラシロキサン/トリフルオロプロピルシクロペンタシロキサン(KF−5002:信越化学工業社製)が挙げられる。 Specifically, as a linear thing, FL-100, X-22-819, X-22-820, X-22-821, X-22-822 (made by Shin-Etsu Chemical Co., Ltd.), FS-1265 (Toray Dow Corning). Examples of cyclic compounds include those described in JP-A-09-268110. For example, trifluoropropylcyclotetrasiloxane / trifluoropropylcyclopentasiloxane (KF) under the INCI name (International Nomenclature Cosmetic Labeling Names). -5002: manufactured by Shin-Etsu Chemical Co., Ltd.).
本発明において、成分(A)の特定のシリコーン重合物は、成分(B)のフルオロアルキル基含有オルガノポリシロキサンと混練することにより、ペースト状の組成物を得ることができる。予め、成分(A)と成分(B)を混練した組成物を製造することにより、メイクアップ化粧料の製造時のハンドリングが向上し、その結果、前記したメイク落ち効果、使用性、使用感を有する安定なメイクアップリムーバー組成物が得られることから好ましい。 In the present invention, the specific silicone polymer of component (A) can be kneaded with the fluoroalkyl group-containing organopolysiloxane of component (B) to obtain a paste-like composition. By preparing a composition in which the component (A) and the component (B) are kneaded in advance, the handling during the production of the makeup cosmetic is improved. As a result, the above-described makeup removal effect, usability, and feeling of use are improved. It is preferable because a stable makeup remover composition is obtained.
前記ペースト状の組成物を得るには、通常の攪拌機で行っても構わないが、剪断力下の混練処理を行うことが好ましい。これは特定のシリコーン重合物が有機溶媒不溶の三次元架橋構造を有しているため、成分(B)のフルオロアルキル基含有オルガノポリシロキサンに均一溶解せず、剪断力下で充分な分散性を与えることにより、外観が滑らかなペースト状組成物が得られるためである。混練処理としては、例えば3本ロール、2本ロール、サンドグラインダー、コロイドミル、高粘度ミキサー、ガウリンホモジナイザー、ディスパー等で行うことができるが、好ましくは3本ロール、高粘度ミキサー、ディスパーによる方法が好ましい。 In order to obtain the paste-like composition, a normal stirrer may be used, but it is preferable to perform a kneading treatment under a shearing force. This is because a specific silicone polymer has a three-dimensional crosslinked structure insoluble in an organic solvent, so that it does not dissolve uniformly in the fluoroalkyl group-containing organopolysiloxane of component (B), and has sufficient dispersibility under shear force. This is because a paste-like composition having a smooth appearance can be obtained. The kneading treatment can be performed with, for example, a three-roll, two-roll, sand grinder, colloid mill, high-viscosity mixer, Gaurin homogenizer, disper, etc., preferably a method using a three-roll, high-viscosity mixer, and disper. preferable.
得られたペースト状の組成物のメイクアップリムーバー組成物中への配合量は、通常は0.1〜90%であり、好ましくは1〜70%である。この範囲であれば、メイク落しの効果に優れ、使用性も安定性も良好なメイクアップリムーバー組成物が得られる。また、ペースト状組成物を製造する場合、成分(A)と成分(B)の質量比は、5:95〜50:50が好ましく、更に好ましくは、10:90〜30:70である。この範囲であれば、メイクアップリムーバー組成物の安定性や使用性がより向上する。 The blending amount of the obtained paste-like composition in the makeup remover composition is usually 0.1 to 90%, preferably 1 to 70%. If it is this range, the makeup remover composition which is excellent in the effect of makeup removal, and is excellent in usability and stability can be obtained. Moreover, when manufacturing a paste-form composition, 5: 95-50: 50 is preferable and, as for mass ratio of a component (A) and a component (B), More preferably, it is 10: 90-30: 70. If it is this range, the stability and usability of a makeup remover composition will improve more.
本発明のメイクアップリムーバー組成物には、成分(C)揮発性液状油を更に配合することができる。本発明で用いられる成分(C)の揮発性液状油は、低粘度でメイクアップ化粧料とのなじみが良く、更には使用後の油性感やべたつきを緩和するのに効果的に用いられる。本発明で用いられる成分(C)の揮発性液状油は化粧料に用いられるものでは特に限定はされないが、成分(A)の特定のシリコーン重合物や成分(B)のフルオロアルキル基含有オルガノポリシロキサンとの配合適正を考慮して、イソヘキサデカン、イソドデカン及びそれらの混合物から選択される軽質流動イソパラフィン、オクタメチルシクロテトラシロキサン、デカメチルシクロペンタシロキサン及びドデカメチルシクロヘキサシロキサンから選択される環状ジメチルポリシロキサン、オクタメチルトリシロキサン、デカメチルテトラシロキサン、ドデカメチルペンタシロキサン、ヘプタメチルオクチルトリシロキサンから選択されるオルガノポリシロキサンが好ましい。これらの揮発性液状油は一種又は二種以上を用いることができる。また、これらの揮発性液状油のメイクアップリムーバー組成物中への配合量は、通常は0.01〜40.0%であり、油性感やべたつきの緩和、安定性、粘性のコントロールのし易さなどから好ましくは0.1〜30.0%である。 The makeup remover composition of the present invention may further contain component (C) volatile liquid oil. The volatile liquid oil of component (C) used in the present invention has a low viscosity and is well-suited to makeup cosmetics. Further, it is effectively used to relieve oiliness and stickiness after use. The volatile liquid oil of component (C) used in the present invention is not particularly limited as long as it is used in cosmetics, but specific silicone polymer of component (A) and fluoroalkyl group-containing organopolypropylene of component (B). In consideration of the suitability for blending with siloxane, a cyclic dimethylpolysiloxane selected from light liquid isoparaffin, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane and dodecamethylcyclohexasiloxane selected from isohexadecane, isododecane and mixtures thereof. Organopolysiloxanes selected from siloxane, octamethyltrisiloxane, decamethyltetrasiloxane, dodecamethylpentasiloxane, and heptamethyloctyltrisiloxane are preferred. These volatile liquid oils can be used singly or in combination. In addition, the blending amount of these volatile liquid oils into the makeup remover composition is usually 0.01 to 40.0%, and it is easy to control oiliness, stickiness, stability and viscosity. From the above, it is preferably 0.1 to 30.0%.
本発明のメイクアップリムーバー組成物には、上記成分の他に、本発明の効果を妨げない範囲で通常の化粧料に使用される成分、水、アルコール類、水溶性高分子、皮膜形成剤、界面活性剤、粉体、樹脂、紫外線吸収剤、保湿剤、防腐剤、抗菌剤、香料、塩類、酸化防止剤、pH調整剤、キレート剤、清涼剤、抗炎症剤、美肌用成分(美白剤、細胞賦活剤、肌荒れ改善剤、血行促進剤、皮膚収斂剤、抗脂漏剤等)、ビタミン類、アミノ酸類、核酸、ホルモン、包接化合物等を添加することができる。 In the makeup remover composition of the present invention, in addition to the above-mentioned components, components that are used in ordinary cosmetics within a range that does not interfere with the effects of the present invention, water, alcohols, water-soluble polymers, film forming agents, Surfactant, powder, resin, UV absorber, moisturizer, antiseptic, antibacterial agent, fragrance, salt, antioxidant, pH adjuster, chelating agent, refreshing agent, anti-inflammatory agent, skin cleansing agent (whitening agent Cell activators, skin roughness improving agents, blood circulation promoters, skin astringents, antiseborrheic agents, etc.), vitamins, amino acids, nucleic acids, hormones, inclusion compounds and the like can be added.
本発明のメイクアップリムーバー組成物は、液状、乳液状、固形状、ペースト状、ゲル状等の形態を適宜選択することができ、また、ふき取り用、洗い流し用等何れの使用方法でのメイクアップリムーバーにも用いることができる。
本発明のメイクアップリムーバー組成物は、通常の化粧料を製造する方法にて製造されるものであり、その製造方法は限定されない。
The makeup remover composition of the present invention can be appropriately selected from liquid, emulsion, solid, paste, gel and other forms, and can be used with any method of use such as wiping or washing off. It can also be used for removers.
The makeup remover composition of the present invention is produced by a method for producing a normal cosmetic, and the production method is not limited.
以下、本発明に関して、合成例及びそれを応用した実施例を挙げて説明するが、本発明はこれらによって何ら限定されるものではない。 Hereinafter, although a synthesis example and the Example which applied it are given and demonstrated regarding this invention, this invention is not limited at all by these.
合成例1 シリコーン重合物1
反応器中に下記平均組成式(4)
Synthesis Example 1 Silicone Polymer 1
In the reactor, the following average composition formula (4)
合成例2 シリコーン重合物2
反応器中に下記平均組成式(6)
Synthesis Example 2 Silicone polymer 2
In the reactor, the following average composition formula (6)
製造例1 ペースト状組成物1の調製
合成例1のシリコーン重合物1を20重量部と、テトラ−3,3,3−トリフルオロプロピルテトラメチルシクロテトラシロキサン/ペンタ−3,3,3−トリフルオロプロピルペンタメチルシクロペンタシロキサン混合物(1/1重量比、粘度60mm2/s)80重量部を混合し、3本ロールで充分混練することにより、チキソトロピー性を持つ、半透明なペースト状組成物1を得た。このペースト状組成物1は、安定性に優れ50℃で1ヶ月後も油性成分の分離や排液は観察されなかった。
Production Example 1 Preparation of Paste Composition 1 20 parts by weight of the silicone polymer 1 of Synthesis Example 1 and tetra-3,3,3-trifluoropropyltetramethylcyclotetrasiloxane / penta-3,3,3-tri A semitransparent paste-like composition having thixotropic properties by mixing 80 parts by weight of a fluoropropylpentamethylcyclopentasiloxane mixture (1/1 weight ratio, viscosity 60 mm 2 / s) and sufficiently kneading with three rolls. 1 was obtained. This pasty composition 1 was excellent in stability, and separation of oily components and drainage were not observed even after one month at 50 ° C.
製造例2 ペースト状組成物2の調製
合成例2のシリコーン重合物2を30重量部と、下記平均組成式(8)
Production Example 2 Preparation of Pasty Composition 2 30 parts by weight of the silicone polymer 2 of Synthesis Example 2 and the following average composition formula (8)
実施例1〜3及び比較例1〜3 メイクアップリムーバー(ふき取りタイプ)
表1に示す組成のメイクアップリムーバー組成物を調製し、その使用感及び使用性について下記の方法に従い、評価を行なった。
Examples 1-3 and Comparative Examples 1-3 Makeup remover (wipe-off type)
A makeup remover composition having the composition shown in Table 1 was prepared, and the feeling of use and usability were evaluated according to the following methods.
(評価方法)
女性20名の専門パネルにより、使用テストを実施し、メイクアップ化粧料(市販のロングラスティング口紅)とのなじみの速さ、落としやすさ、使用時の油性感のなさ、後肌のべたつきのなさに関してパネル各人が下記絶対評価にて7段階に評価し評点を付け、試料毎にパネル全員の評点合計から、その平均値を算出し、下記4段階判定基準により判定した。得られた結果を表1に併せて示す。
(Evaluation methods)
A professional panel of 20 women conducts a usage test and is quick to apply with makeup cosmetics (commercially available long-lasting lipstick), easy to remove, lack of oiliness when used, and sticky to the back skin Each panel member gave an evaluation based on the following absolute evaluation and assigned a score, and the average value was calculated from the total score of all the panel members for each sample, and judged according to the following four-step criteria. The obtained results are also shown in Table 1.
(絶対評価)
(評点):(評価)
6:非常に良い
5:良い
4:やや良い
3:普通
2:やや悪い
1:悪い
0:非常に悪い
(4段階判定基準)
(評点平均値) :(判定)
5点を超える :非常に良好:◎
3点を超えて5点以下:良好 :○
1点を超えて3点以下:やや不良 :△
1点以下 :不良 :×
(Absolute evaluation)
(Score): (Evaluation)
6: Very good 5: Good 4: Somewhat good 3: Normal 2: Somewhat bad 1: Bad 0: Very bad (4 step criteria)
(Average score): (Judgment)
More than 5 points: Very good: ◎
3 points to 5 points or less: Good: ○
More than 1 point and 3 points or less: Somewhat bad: △
1 point or less: Defect: ×
(安定性評価)
40℃に各サンプルをセットし、一ヵ月後の外観を目視にて観察し評価した。
(判定基準)
○:外観上変化なし
△:キメや外観にわずかに変化が見られる。
×:明らかに分離や凝集が見られる。
(Stability evaluation)
Each sample was set at 40 ° C., and the appearance after one month was visually observed and evaluated.
(Criteria)
○: No change in appearance Δ: Slight change in texture and appearance
X: Separation and aggregation are clearly observed.
(製造方法)
A:成分1〜6を均一に混合する。
B:Aに成分7〜10を加え均一に混合する。
(Production method)
A: Components 1 to 6 are mixed uniformly.
B: Components 7 to 10 are added to A and mixed uniformly.
表1の結果から明らかなように、本発明のふき取りタイプのメイクアップリムーバー(実施例1〜3)は、耐水性、耐油性が高く落としにくいロングラスティング口紅とのなじみが速く、口紅落ちも良く、使用中の油性感もなく、ふき取り後の肌もべたつかないなどの使用性、使用感に優れるものであった。一方、成分(A)の特定のシリコーン重合物と成分(B)のフルオロアルキル基含有オルガノポリシロキサンを用いない比較例1〜3は、全ての評価項目で劣るが、特にロングラスティング口紅の落としやすさに劣るものであった。また、フッ素化合物であるパーフルオロポリエーテルを加えた比較例3では、経時安定性も良くなかった。 As is apparent from the results in Table 1, the wipe-off type makeup remover (Examples 1 to 3) of the present invention has a high water resistance and oil resistance and is easy to remove with the long lasting lipstick, and the lipstick is also removed. It was excellent in usability and usability, such as no oiliness during use and no skin stickiness after wiping. On the other hand, Comparative Examples 1 to 3 in which the specific silicone polymer of component (A) and the fluoroalkyl group-containing organopolysiloxane of component (B) are not used are inferior in all the evaluation items. It was inferior to ease. Further, in Comparative Example 3 in which perfluoropolyether which is a fluorine compound was added, the temporal stability was not good.
実施例4〜5及び比較例4〜5 メイクアップリムーバー(洗い流しタイプ)
表2に示す組成の洗い流しタイプのメイクアップリムーバーを調製し、前述の評価方法に従い、女性20名の専門パネルにより使用テストを実施し、手へのとりやすさ、メイクアップ化粧料(市販のW/Oリキッドファンデーション)とのなじみの速さ、落としやすさ、使用時の油性感のなさ、使用時の油性感のなさ、後肌のべたつきのなさについて下記の方法に従い、評価を行った。また安定性評価も前述の判定基準に従って実施した。得られた結果を表2に併せて示す。
Examples 4 to 5 and Comparative Examples 4 to 5 Makeup remover (wash-out type)
A wash-off type makeup remover having the composition shown in Table 2 was prepared, and a use test was conducted by a professional panel of 20 women according to the evaluation method described above. / O Liquid Foundation) was evaluated according to the following methods for ease of removal, ease of removal, lack of oiliness during use, lack of oiliness during use, and non-stickiness of the back skin. The stability evaluation was also performed according to the aforementioned criteria. The obtained results are also shown in Table 2.
(製造方法)
A:成分1〜3及び成分7、8均一に混合する。
B:成分4〜6及び成分9〜11を均一に混合する。
C:AとBを均一に混合する。
(Production method)
A: Components 1 to 3 and components 7 and 8 are mixed uniformly.
B: Components 4 to 6 and components 9 to 11 are mixed uniformly.
C: A and B are mixed uniformly.
表2の結果から明らかなように、本発明の洗い流しタイプのメイクアップリムーバー(実施例4〜5)は、手にとりやすく、耐水性、耐油性が高く落としにくいW/Oリキッドファンデーションとのなじみが速く、洗い流し後の肌もべたつかないなどの使用性、使用感に優れるものであった。特に実施例5の成分(C)の揮発性液状油である軽質流動イソパラフィンを含有するものが、使用中の油性感のなさ、後肌のべたつきのなさでは勝っていた。一方、成分(A)の特定のシリコーン重合物と成分(B)のフルオロアルキル基含有オルガノポリシロキサンを用いない比較例4〜5では、ほとんどの評価で劣るが、特にW/Oリキッドファンデーション落としやすさに劣るものであった。また、成分(B)のフルオロアルキル基含有オルガノポリシロキサンのみ含有する比較例5では、経時安定性も良くなかった。 As is apparent from the results in Table 2, the wash-off type makeup remover of the present invention (Examples 4 to 5) is easy to take, has high water resistance and oil resistance, and is familiar with the W / O liquid foundation. It was fast and excellent in usability and feeling of use, such as non-sticky skin after washing. In particular, those containing light liquid isoparaffin, which is the volatile liquid oil of component (C) of Example 5, were superior in terms of lack of oiliness during use and stickiness of the back skin. On the other hand, Comparative Examples 4 to 5 in which the specific silicone polymer of component (A) and the fluoroalkyl group-containing organopolysiloxane of component (B) are not used are inferior in most evaluations, but it is particularly easy to drop the W / O liquid foundation. It was inferior. Further, in Comparative Example 5 containing only the fluoroalkyl group-containing organopolysiloxane of the component (B), the temporal stability was not good.
実施例6 メイクアップリムーバー(ローションタイプ)
(成分) (%)
1.グリセリン 30.0
2.1,3−ブチレングリコール 30.0
3.ポリエチレングリコール400 20.0
4.ポリオキシエチレン(60)硬化ヒマシ油 8.0
5.軽質流動イソパラフィン*8 3.0
6.ペースト状組成物1(製造例1) 0.5
7.防腐剤 適量
8.香料 適量
9.精製水 残量
*8:IPソルベント1620(出光石油化学社製)
Example 6 Makeup Remover (Lotion Type)
(Ingredient) (%)
1. Glycerin 30.0
2. 1,3-butylene glycol 30.0
3. Polyethylene glycol 400 20.0
4). Polyoxyethylene (60) hydrogenated castor oil 8.0
5). Light liquid isoparaffin * 8 3.0
6). Pasty composition 1 (Production Example 1) 0.5
7). Preservative appropriate amount 8. Perfume appropriate amount 9. Purified water remaining amount * 8: IP solvent 1620 (manufactured by Idemitsu Petrochemical Co., Ltd.)
(製造方法)
A:成分3〜4と成分9を混合し、加温溶解する。
B:成分5〜6を混合する。
C:A、B、成分1〜2及び成分7〜8を攪拌混合して、ローションタイプのメイクアップリムーバーを得た。
本発明のローションタイプのメイクアップリムーバーは、コットンに取り、メイクアップ化粧料となしませると、特にロングラスティングタイプのメイクアップ化粧料とのなじみが速く、メイク落ちが良好であり、洗い流した後の肌は、べたつきがなくさっぱりとして使用性、使用感に優れたものであった。
(Production method)
A: Components 3 to 4 and 9 are mixed and dissolved by heating.
B: Components 5 to 6 are mixed.
C: A, B, components 1-2, and components 7-8 were stirred and mixed to obtain a lotion type makeup remover.
The lotion type make-up remover of the present invention, when taken on cotton and made into makeup cosmetics, is particularly familiar with long-lasting type makeup cosmetics, has good makeup removal, and is washed off. The skin had no stickiness and was refreshing and excellent in usability and usability.
実施例7 メイクアップリムーバー(ジェルタイプ)
(成分) (%)
1.グリセリン 20.0
2.1,3−ブチレングリコール 10.0
3.ポリエチレングリコール1500 5.0
4.エタノール 5.0
5.アクリル酸・アクリル酸アルキル(C10−30)
コポリマー*9 0.3
6.トリエタノールアミン 0.3
7.ペーストの状組成物2(製造例2) 10.0
8.ヘプタメチルオクチルトリシロキサン*10 5.0
9.防腐剤 適量
10.香料 適量
11.精製水 残量
*9:カーボポール1342(グッドリッチケミカル社製)
*10:SILSOFT 034(日本ユニカー社製)
Example 7 Makeup Remover (Gel Type)
(Ingredient) (%)
1. Glycerin 20.0
2. 1,3-butylene glycol 10.0
3. Polyethylene glycol 1500 5.0
4). Ethanol 5.0
5). Acrylic acid and alkyl acrylate (C10-30)
Copolymer * 9 0.3
6). Triethanolamine 0.3
7). Pasty composition 2 (Production Example 2) 10.0
8). Heptamethyloctyltrisiloxane * 10 5.0
9. Preservative appropriate amount10. Perfume proper amount11. Purified water remaining * 9: Carbopol 1342 (manufactured by Goodrich Chemical)
* 10: SILSOFT 034 (Nihon Unicar)
(製造方法)
A:成分3と成分11を混合し、加温溶解する。
B:成分7〜10を混合する。
C:Aと成分1〜2及び成分4〜5を攪拌混合後、成分6を加えて混合する。
D:CにBを添加して攪拌混合し、ジェルタイプのメイクアップリムーバーを得た。
本発明のジェルタイプのメイクアップリムーバーは、手にとり易く、特にロングラスティングタイプのメイクアップ化粧料とのなじみが速く、メイク落ちが良好であり、拭き取った後の肌は、べたつきがなくさっぱりとして使用性、使用感に優れたものであった。
(Production method)
A: Component 3 and component 11 are mixed and dissolved by heating.
B: Components 7 to 10 are mixed.
C: After stirring and mixing A with components 1-2 and 4-5, component 6 is added and mixed.
D: B was added to C and mixed with stirring to obtain a gel-type makeup remover.
The gel-type makeup remover of the present invention is easy to take, especially with the long lasting type makeup cosmetics, has good makeup removal, and the skin after wiping is not sticky and refreshing It was excellent in usability and usability.
実施例8 メイクアップリムーバー(クリームタイプ)
(成分) (%)
1.ステアリン酸 2.0
2.セタノール 5.0
3.流動パラフィン 20.0
4.トリオクタン酸グリセリル 10.0
5.部分架橋型ジメチルポリシロキサン/デカメチルシクロ
ペンタシロキサン混合物*11 5.0
6.ペースト状組成物1(製造例1) 5.0
7.1,3−ブチレングリコール 10.0
8.モノステアリン酸グリセリン 2.0
9.ポリオキシエチレン(20)ソルビタン
モノステアリン酸エステル 2.0
10.水酸化カリウム 0.1
11.防腐剤 適量
12.香料 適量
13.精製水 残量
*11:KSG−15(信越化学工業社製)
Example 8 Makeup Remover (Cream Type)
(Ingredient) (%)
1. Stearic acid 2.0
2. Cetanol 5.0
3. Liquid paraffin 20.0
4). Glyceryl trioctanoate 10.0
5). Partially crosslinked dimethylpolysiloxane / decamethylcyclopentasiloxane mixture * 11 5.0
6). Pasty composition 1 (Production Example 1) 5.0
7.1,3-Butylene glycol 10.0
8). Glycerol monostearate 2.0
9. Polyoxyethylene (20) sorbitan monostearate 2.0
10. Potassium hydroxide 0.1
11. Preservative appropriate amount 12. Perfume appropriate amount13. Purified water remaining amount * 11: KSG-15 (manufactured by Shin-Etsu Chemical Co., Ltd.)
(製造方法)
A:成分1〜4を加温溶解後、成分5〜6、成分8〜9及び成分11〜12を加えて均一に混合し、80℃に調整する。
B:成分7、成分10及び成分13を均一に混合し、80℃に調整する。
C:BにAを添加しながら乳化後、冷却してクリームタイプのメイクアップリムーバーを得た。
本発明のクリームタイプのメイクアップリムーバーは、手にとり易く、特にロングラスティングタイプのメイクアップ化粧料とのなじみが速く、メイク落ちが良好であり、拭き取った後の肌は、べたつきがなく適度にしっとりとして使用性、使用感に優れたものであった。
(Production method)
A: Components 1 to 4 are heated and dissolved, then components 5 to 6, components 8 to 9, and components 11 to 12 are added and mixed uniformly, and adjusted to 80 ° C.
B: Components 7, 10, and 13 are mixed uniformly and adjusted to 80 ° C.
C: After emulsification while adding A to B, the mixture was cooled to obtain a cream type makeup remover.
The cream-type makeup remover of the present invention is easy to take, especially with the long lasting type makeup cosmetics, has good makeup removal, and the skin after wiping off has no stickiness and is moderate It was moist and excellent in usability and usability.
実施例9 オイルクレンジング
(成分) (%)
1.2−エチルヘキサン酸セチル 20.0
2.(ベヘン酸/エイコサン二酸)グリセリル*12 3.0
3.(パルミチン酸/2−エチルへキサン酸)デキストリン*13 2.0
4.ペースト状の組成物2(製造例2) 2.0
5.ドデカメチルペンタシロキサン*14 5.0
6.トリオレイン酸ポリオキシエチレン(20)ソルビタン 5.0
7.軽質流動イソパラフィン*15 5.0
8.流動パラフィン 残量
9.香料 適量
*12:ノムコートHK−G(日清オイリオ社製)
*13:レオパールTT(千葉製粉社製)
*14:KF−96L−2cs(信越化学工業社製)
*15:IPソルベント2028(出光石油化学社製)
Example 9 Oil cleansing (ingredient) (%)
Cetyl 1.2-ethylhexanoate 20.0
2. (Behenic acid / eicosanedioic acid) glyceryl * 12 3.0
3. (Palmitic acid / 2-ethylhexanoic acid) dextrin * 13 2.0
4). Pasty composition 2 (Production Example 2) 2.0
5). Dodecamethylpentasiloxane * 14 5.0
6). Polyoxyethylene trioleate (20) sorbitan 5.0
7). Light liquid isoparaffin * 15 5.0
8). 8. Liquid paraffin remaining Perfume appropriate amount * 12: Nomucoat HK-G (Nisshin Oilio Co., Ltd.)
* 13: Leopard TT (Chiba Flour Mills)
* 14: KF-96L-2cs (manufactured by Shin-Etsu Chemical Co., Ltd.)
* 15: IP solvent 2028 (made by Idemitsu Petrochemical Co., Ltd.)
(製造方法)
A:成分1〜9を加温溶解して均一に混合後、冷却してオイルクレンジングを得る。
本発明品のオイルクレンジングは、ジェル状で手にとり易く、特にロングラスティングタイプのメイクアップ化粧料とのなじみが速く、メイク落ちが良好であり、拭き取った後の肌は、油性感、べたつきがなく使用性、使用感に優れたものであった。
(Production method)
A: Components 1 to 9 are heated and dissolved, mixed uniformly, and then cooled to obtain oil cleansing.
The oil cleansing of the present invention is gel-like and easy to take, especially with the long lasting type makeup cosmetics, has good makeup removal, and the skin after wiping is oily and sticky It was excellent in usability and usability.
Claims (4)
(A)下記一般式(1)で示されるオルガノハイドロジェンポリシロキサン
R1 aHbSiO(4−a−b)/2(1)
と、下記一般式(2)で示されるオルガノポリシロキサン
R1 cR2 dSiO(4−c−d)/2(2)
を重合してなり、有機溶剤に不溶で、かつ自重と同質量以上のペンタ−3,3,3−トリフロロプロピルペンタメチルシクロペンタシロキサンを含みうることを特徴とする三次元架橋構造を有するシリコーン重合物〔但し、式中R1はそれぞれ同じか又は異なってもよく、脂肪族不飽和結合を有しない、置換又は非置換の、炭素数1〜20の一価炭化水素基であって、その11〜60モル%がフッ素置換一価炭化水素基である一価炭化水素基であり、R2は末端ビニル基を有する炭素数2〜10の一価炭化水素基であり、aは1.0から2.3、bは0.001〜1.0、cは1.0〜2.3、dは0.001〜1.0であって、1.5≦a+b≦2.6、1.5≦c+d≦2.6を満たす。〕
(B)フルオロアルキル基含有オルガノポリシロキサン
を含有するメイクアップリムーバー組成物。 The following components (A) to (B):
(A) Organohydrogenpolysiloxane represented by the following general formula (1) R 1 a H b SiO (4-ab) / 2 (1)
And organopolysiloxane R 1 c R 2 d SiO (4-cd) / 2 (2) represented by the following general formula (2):
A silicone having a three-dimensional cross-linking structure, characterized in that it can contain penta-3,3,3-trifluoropropylpentamethylcyclopentasiloxane that is insoluble in an organic solvent and has the same mass or more as its own weight. Polymers wherein R 1 may be the same or different and each is a substituted or unsubstituted monovalent hydrocarbon group having 1 to 20 carbon atoms and having no aliphatic unsaturated bond, 11 to 60 mol% is a monovalent hydrocarbon group which is a fluorine-substituted monovalent hydrocarbon group, R 2 is a monovalent hydrocarbon group having 2 to 10 carbon atoms having a terminal vinyl group, and a is 1.0 2.3, b is 0.001 to 1.0, c is 1.0 to 2.3, d is 0.001 to 1.0, and 1.5 ≦ a + b ≦ 2.6. 5 ≦ c + d ≦ 2.6 is satisfied. ]
(B) A makeup remover composition containing a fluoroalkyl group-containing organopolysiloxane.
である請求項1記載のメイクアップリムーバー組成物。 The component (B) fluoroalkyl group-containing organopolysiloxane according to claim 1 is represented by the following general formula (3):
The makeup remover composition according to claim 1.
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|---|---|---|---|
| JP2005038502A JP2005314358A (en) | 2004-03-31 | 2005-02-16 | Make up remover composition |
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| JP2004103453 | 2004-03-31 | ||
| JP2005038502A JP2005314358A (en) | 2004-03-31 | 2005-02-16 | Make up remover composition |
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| WO2007058825A1 (en) * | 2005-11-15 | 2007-05-24 | Momentive Performance Materials Inc. | Swollen silicone composition and process of producing same |
| WO2007061623A1 (en) * | 2005-11-15 | 2007-05-31 | Momentive Performance Materials Inc. | Swollen silicone composition, process of producing same and products thereof |
| FR2910304A1 (en) * | 2006-12-20 | 2008-06-27 | Oreal | Removing make-up, e.g. non-transfer lipstick or color foundation, by applying silicone-forming reactive components and optionally catalyst or peroxide and removing obtained film |
| JP2008184414A (en) * | 2007-01-29 | 2008-08-14 | Kao Corp | Cleansing composition |
| WO2009153963A1 (en) * | 2008-06-19 | 2009-12-23 | 株式会社 資生堂 | Cleansing cosmetic preparation |
| US7723414B2 (en) | 2006-12-22 | 2010-05-25 | E. I. Du Pont De Nemours And Company | Antistatic system for polymers |
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| US7863361B2 (en) | 2005-11-15 | 2011-01-04 | Momentive Performance Materials Inc. | Swollen silicone composition, process of producing same and products thereof |
| KR101441552B1 (en) | 2005-11-15 | 2014-09-17 | 모멘티브 퍼포먼스 머티리얼즈 인크. | Swollen silicone composition, process of producing same and products thereof |
| CN101360476B (en) * | 2005-11-15 | 2015-08-05 | 莫门蒂夫性能材料股份有限公司 | Swellable silicone composition, its preparation method and its products |
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| CN101360476A (en) * | 2005-11-15 | 2009-02-04 | 莫门蒂夫性能材料股份有限公司 | Swollen silicone composition, method of making, and article thereof |
| WO2007058825A1 (en) * | 2005-11-15 | 2007-05-24 | Momentive Performance Materials Inc. | Swollen silicone composition and process of producing same |
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| EP2228053A1 (en) * | 2005-11-15 | 2010-09-15 | Momentive Performance Materials Inc. | Swollen silicone composition and process of producing same |
| WO2007061623A1 (en) * | 2005-11-15 | 2007-05-31 | Momentive Performance Materials Inc. | Swollen silicone composition, process of producing same and products thereof |
| FR2910304A1 (en) * | 2006-12-20 | 2008-06-27 | Oreal | Removing make-up, e.g. non-transfer lipstick or color foundation, by applying silicone-forming reactive components and optionally catalyst or peroxide and removing obtained film |
| US7723414B2 (en) | 2006-12-22 | 2010-05-25 | E. I. Du Pont De Nemours And Company | Antistatic system for polymers |
| JP2008184414A (en) * | 2007-01-29 | 2008-08-14 | Kao Corp | Cleansing composition |
| WO2009153963A1 (en) * | 2008-06-19 | 2009-12-23 | 株式会社 資生堂 | Cleansing cosmetic preparation |
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| CN106038359A (en) * | 2008-06-19 | 2016-10-26 | 株式会社资生堂 | Cleansing cosmetic |
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