JP2013256476A5 - - Google Patents
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- Publication number
- JP2013256476A5 JP2013256476A5 JP2012134612A JP2012134612A JP2013256476A5 JP 2013256476 A5 JP2013256476 A5 JP 2013256476A5 JP 2012134612 A JP2012134612 A JP 2012134612A JP 2012134612 A JP2012134612 A JP 2012134612A JP 2013256476 A5 JP2013256476 A5 JP 2013256476A5
- Authority
- JP
- Japan
- Prior art keywords
- fatty acid
- cosmetic
- solubilized
- acid ester
- polyglycerin fatty
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 239000002537 cosmetic Substances 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 6
- 239000000194 fatty acid Substances 0.000 claims description 6
- -1 fatty acid ester Chemical class 0.000 claims description 6
- 239000000419 plant extract Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N Stearic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
- 150000004665 fatty acids Chemical group 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- POULHZVOKOAJMA-UHFFFAOYSA-N Lauric acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N Palmitic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 229920000223 polyglycerol Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000005639 Lauric acid Substances 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 125000004432 carbon atoms Chemical group C* 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000003381 solubilizing Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
Description
＜本発明のポリグリセリン脂肪酸エステル＞
本発明の可溶化型化粧料は、必須成分としてポリグリセリン脂肪酸エステルを含有することを特徴とする。かかる成分は、水溶性の植物抽出エキスを可溶化せしめ、高い透明性を付与する作用を有する。前記ポリグリセリン脂肪酸エステルの脂肪酸残基としては、炭素数１０〜１８の直鎖、分岐又は環状構造を有するものが好ましく例示できる。このような脂肪酸残基としては、例えば、ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸、イソステアリン酸等が好ましく例示できる。これらの中ではイソステアリン酸が特に好ましい。又、ポリグリセリンとしては、グリセリンの平均重合度が２〜９のものが好ましく、３〜５のものが特に好ましい。かかるポリグリセリンのフリーの水酸基の内、前記脂肪酸残基で修飾されるものは半分以下であることが好ましい。具体的には、本発明の可溶化型化粧料においては、平均重合度が３のジイソステアリン酸ポリグリセリルが好ましく例示できる。かかる成分は、市販されているものを使用することもできる。このようなポリグリセリン脂肪酸エステルとしては、高級アルコール工業株式会社製の「リソレックスＰＧＩＳ３２」等が好ましく例示される。本発明の可溶化型化粧料においては、かかる成分は化粧料全体に対して０．５質量％より多く５質量％以下含有されることが好ましく、より好ましくは１質量％以上３質量％以下含有される。この範囲を外れると、水溶性の植物抽出エキスの可溶化の安定性が著しく低下する。
<Polyglycerin fatty acid ester of the present invention>
The solubilized cosmetic of the present invention is characterized by containing a polyglycerol fatty acid ester as an essential component. Such components have the effect of solubilizing water-soluble plant extract and imparting high transparency. Preferred examples of the fatty acid residue of the polyglycerin fatty acid ester include those having a linear, branched or cyclic structure having 10 to 18 carbon atoms. Preferred examples of such fatty acid residues include lauric acid, myristic acid, palmitic acid, stearic acid, and isostearic acid. Of these, isostearic acid is particularly preferred. As the polyglycerol, those having an average degree of polymerization of glycerol of 2 to 9 are preferable, and those of 3 to 5 are particularly preferable. Among the free hydroxyl groups of polyglycerin, those modified with the fatty acid residue are preferably less than half. Specifically, in the solubilized cosmetic of the present invention, polyglyceryl diisostearate having an average degree of polymerization of 3 can be preferably exemplified. As this component, a commercially available product can be used. As such a polyglycerin fatty acid ester, “Risolex PGIS32” manufactured by Higher Alcohol Industry Co., Ltd. is preferably exemplified. In solubilized cosmetic composition of the present invention, such components contain preferably Rukoto contained most 5 wt% or less than 0.5 wt% based on the total cosmetic, more preferably 1 wt% to 3 wt% or less Is done. Outside this range, the solubilization stability of the water-soluble plant extract is significantly reduced.
Claims (3)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2012134612A JP6088158B2 (en) | 2012-06-14 | 2012-06-14 | Solubilized cosmetics |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2012134612A JP6088158B2 (en) | 2012-06-14 | 2012-06-14 | Solubilized cosmetics |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013256476A JP2013256476A (en) | 2013-12-26 |
| JP2013256476A5 true JP2013256476A5 (en) | 2015-07-23 |
| JP6088158B2 JP6088158B2 (en) | 2017-03-01 |
Family
ID=49953240
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012134612A Active JP6088158B2 (en) | 2012-06-14 | 2012-06-14 | Solubilized cosmetics |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP6088158B2 (en) |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5910505A (en) * | 1982-07-07 | 1984-01-20 | Nisshin Oil Mills Ltd:The | Oily beautifying cosmetic |
| JP2752712B2 (en) * | 1989-08-08 | 1998-05-18 | ポーラ化成工業株式会社 | Solubilized cosmetic |
| JP2002179526A (en) * | 2000-12-08 | 2002-06-26 | Sakamoto Yakuhin Kogyo Co Ltd | Gel-shaped cleansing cosmetic |
| JP3964760B2 (en) * | 2002-08-12 | 2007-08-22 | 花王株式会社 | Cleansing cosmetics |
| JP2004337083A (en) * | 2003-05-16 | 2004-12-02 | Sakamoto Yakuhin Kogyo Co Ltd | Oil-dissolving agent for water-soluble compound |
| JP2005068027A (en) * | 2003-08-27 | 2005-03-17 | Nippon Menaade Keshohin Kk | Composition for lipstick |
| JP2005213237A (en) * | 2004-02-02 | 2005-08-11 | Sakamoto Yakuhin Kogyo Co Ltd | Transparent liquid cleansing cosmetic |
| JP4188314B2 (en) * | 2004-12-24 | 2008-11-26 | 花王株式会社 | Oil cleansing fee |
| JP4550676B2 (en) * | 2005-06-30 | 2010-09-22 | 花王株式会社 | Cleansing fee |
| JP2007070576A (en) * | 2005-09-09 | 2007-03-22 | Sakamoto Yakuhin Kogyo Co Ltd | Agent for use in dissolving water-soluble compound into oil |
| JP5646132B2 (en) * | 2006-09-29 | 2014-12-24 | 株式会社コーセー | Skin cleanser |
| JP5033567B2 (en) * | 2007-10-01 | 2012-09-26 | 株式会社コーセー | Oil cleansing fee |
-
2012
- 2012-06-14 JP JP2012134612A patent/JP6088158B2/en active Active
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