JP2000080021A - Ultraviolet absorbing pigment for cosmetic and cosmetic - Google Patents
Ultraviolet absorbing pigment for cosmetic and cosmeticInfo
- Publication number
- JP2000080021A JP2000080021A JP10249390A JP24939098A JP2000080021A JP 2000080021 A JP2000080021 A JP 2000080021A JP 10249390 A JP10249390 A JP 10249390A JP 24939098 A JP24939098 A JP 24939098A JP 2000080021 A JP2000080021 A JP 2000080021A
- Authority
- JP
- Japan
- Prior art keywords
- cosmetics
- ultraviolet absorbing
- pigment
- cosmetic
- organic
- 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.)
- Withdrawn
Links
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- 230000002745 absorbent Effects 0.000 claims 1
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- 235000014113 dietary fatty acids Nutrition 0.000 description 1
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- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- HPMLGOFBKNGJAM-ONEGZZNKSA-N ethyl (e)-3-(1h-imidazol-5-yl)prop-2-enoate Chemical compound CCOC(=O)\C=C\C1=CN=CN1 HPMLGOFBKNGJAM-ONEGZZNKSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229940075507 glyceryl monostearate Drugs 0.000 description 1
- 230000037308 hair color Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052864 hemimorphite Inorganic materials 0.000 description 1
- GQXQIRNPJBUEGY-UHFFFAOYSA-N hexadecan-7-yl 2,2-dimethyloctanoate Chemical compound CCCCCCCCCC(CCCCCC)OC(=O)C(C)(C)CCCCCC GQXQIRNPJBUEGY-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 229940100463 hexyl laurate Drugs 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- LDHBWEYLDHLIBQ-UHFFFAOYSA-M iron(3+);oxygen(2-);hydroxide;hydrate Chemical compound O.[OH-].[O-2].[Fe+3] LDHBWEYLDHLIBQ-UHFFFAOYSA-M 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000000865 liniment Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- 229940078812 myristyl myristate Drugs 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000003405 preventing effect Effects 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 150000003870 salicylic acids Chemical class 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000011863 silicon-based powder Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 229910021647 smectite Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- KJCLYACXIWMFCC-UHFFFAOYSA-M sodium;5-benzoyl-4-hydroxy-2-methoxybenzenesulfonate Chemical compound [Na+].C1=C(S([O-])(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 KJCLYACXIWMFCC-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 230000037072 sun protection Effects 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- LOIYMIARKYCTBW-OWOJBTEDSA-N trans-urocanic acid Chemical compound OC(=O)\C=C\C1=CNC=N1 LOIYMIARKYCTBW-OWOJBTEDSA-N 0.000 description 1
- LOIYMIARKYCTBW-UHFFFAOYSA-N trans-urocanic acid Natural products OC(=O)C=CC1=CNC=N1 LOIYMIARKYCTBW-UHFFFAOYSA-N 0.000 description 1
- QPQANCNBWQXGTQ-UHFFFAOYSA-N trihydroxy(trimethylsilylperoxy)silane Chemical compound C[Si](C)(C)OO[Si](O)(O)O QPQANCNBWQXGTQ-UHFFFAOYSA-N 0.000 description 1
- 229960002703 undecylenic acid Drugs 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- CPYIZQLXMGRKSW-UHFFFAOYSA-N zinc;iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Fe+3].[Fe+3].[Zn+2] CPYIZQLXMGRKSW-UHFFFAOYSA-N 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、例えば、ファンデ
ーション,アイシャドウ,ほほ紅等のメイクアップ化粧
料および乳液,クリーム等の基礎化粧料に用いられる化
粧料用紫外線吸収性顔料およびその化粧料用紫外吸収性
顔料を配合してなる化粧料に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an ultraviolet-absorbing pigment for cosmetics used in makeup cosmetics such as foundation, eyeshadow, blusher and the like and basic cosmetics such as emulsions and creams, and for cosmetics. The present invention relates to a cosmetic containing an ultraviolet absorbing pigment.
【0002】[0002]
【従来の技術】従来、ファンデーション,アイシャド
ウ,ほほ紅等のメイクアップ化粧料および乳液,クリー
ム等の基礎化粧料は、その紫外線吸収性を向上させるた
めに、例えば微粒子酸化チタン,微粒子酸化亜鉛等が配
合されたり、または有機系紫外線吸収性化合物等が直接
配合されている。2. Description of the Related Art Conventionally, makeup cosmetics such as foundations, eye shadows, and blushers and basic cosmetics such as emulsions and creams have been used in order to improve the ultraviolet absorption, for example, fine titanium oxide, fine zinc oxide and the like. Or an organic ultraviolet absorbing compound or the like is directly mixed.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、これら
微粒子酸化チタンおよび微粒子酸化亜鉛は、非常に微細
であるため表面活性が非常に高く、そのままで使用する
と容易に凝集を起こして紫外線吸収性能を低下させた
り、化粧料に配合した際の使用感を低下させる問題点が
ある。また、前記微粒子酸化チタンおよび微粒子酸化亜
鉛は、化粧料中の他の有機物質を変質させたり、肌荒れ
を起こす原因となる等の問題点がある。However, these fine particles of titanium oxide and fine particles of zinc oxide have very high surface activity because they are very fine, and if they are used as they are, they easily aggregate to lower the ultraviolet absorption performance. And there is a problem that the feeling of use when blended into cosmetics is reduced. In addition, the fine particle titanium oxide and the fine particle zinc oxide have a problem that they cause deterioration of other organic substances in the cosmetic and cause rough skin.
【0004】また、化粧料に直接有機系紫外線吸収性化
合物を配合した場合には、その有機系紫外線吸収性化合
物が化粧料中に分子状態で均一に分散されることが非常
に困難であり、局所的に有機系紫外線吸収性化合物が存
在するために有機系紫外線吸収性化合物自体の紫外線吸
収性能を最大限に発揮させることがない問題点がある。
また、前記有機系紫外線吸収性化合物が直接皮脂に触れ
ることがあり、溶出して皮脂に吸収されるという危険性
もある。Further, when an organic ultraviolet absorbing compound is directly blended into a cosmetic, it is very difficult for the organic ultraviolet absorbing compound to be uniformly dispersed in a molecular state in the cosmetic. There is a problem in that the organic ultraviolet absorbing compound does not exhibit the ultraviolet absorbing performance of the organic ultraviolet absorbing compound itself to the maximum because the organic ultraviolet absorbing compound exists locally.
In addition, the organic ultraviolet absorbing compound may come into direct contact with sebum, and there is a risk that the compound is eluted and absorbed by the sebum.
【0005】本発明は、このような問題点を解消するた
めになされたもので、安定して分散性が高く、優れた紫
外線吸収効果を有し、かつ肌への影響が少なく感触のよ
い化粧料用紫外線吸収性顔料およびその化粧料用紫外線
吸収性顔料を含有する化粧料を提供することを目的とす
るものである。SUMMARY OF THE INVENTION The present invention has been made to solve such problems, and has a stable and high dispersibility, has an excellent ultraviolet absorbing effect, has a small effect on the skin, and has a good touch. It is an object of the present invention to provide an ultraviolet absorbing pigment for cosmetics and a cosmetic containing the ultraviolet absorbing pigment for cosmetics.
【0006】[0006]
【課題を解決するための手段および作用・効果】前述さ
れた目的を達成するために、本発明による化粧料紫外線
吸収性顔料は、化粧料用顔料粉体に、有機高分子化合物
を媒体として有機系紫外線吸収性化合物を包含被覆させ
ることを特徴とするものである。Means for Solving the Problems and Functions / Effects In order to achieve the above-mentioned object, the cosmetic ultraviolet absorbing pigment according to the present invention is obtained by adding an organic polymer compound as a medium to a pigment powder for cosmetics. The present invention is characterized by including and covering a system ultraviolet absorbing compound.
【0007】本発明においては、化粧料用顔料粉体表面
に有機高分子化合物を媒体として有機系紫外線吸収性化
合物が分子レベルで分散包含被覆処理されている。この
ように有機系紫外線吸収性化合物が分散して存在するた
め、表面活性が非常に低く、有機系紫外線吸収性化合物
自体の紫外線吸収性能を最大限に発揮させることができ
る効果を奏する。また、有機系紫外線吸収性化合物が顔
料粉体の外部に溶出しにくく、化粧料に配合した場合で
あっても他の有機物質を変質させることがなく、溶出し
て皮脂に吸収されることがないため、肌への影響が少な
く安全性が高いという効果を奏する。In the present invention, the surface of the pigment powder for cosmetics is coated with an organic UV-absorbing compound dispersed and covered on a molecular level using an organic polymer compound as a medium. As described above, since the organic ultraviolet absorbing compound is present in a dispersed state, the surface activity is extremely low, and an effect of maximizing the ultraviolet absorbing performance of the organic ultraviolet absorbing compound itself is exhibited. Further, the organic ultraviolet absorbing compound is hardly eluted out of the pigment powder, and does not deteriorate other organic substances even when it is incorporated into cosmetics, and is eluted and absorbed by sebum. There is no effect on the skin, so that there is an effect that the safety is high.
【0008】本発明においては、前記化粧料用顔料粉体
が板状の無機顔料粉体であるのが好ましい。このように
スムーズな感触が得られる化粧料に多く用いられる板状
の無機顔料粉体の表面に有機系紫外線吸収性化合物を分
子レベルで分散包含被覆処理させることにより、前記板
状の顔料粉体のもつスムースな感触を失うことなく極め
て高い紫外線吸収性能を得ることができる効果を奏す
る。In the present invention, the cosmetic pigment powder is preferably a plate-like inorganic pigment powder. The above-mentioned plate-like pigment powder is obtained by dispersing and covering an organic ultraviolet absorbing compound at the molecular level on the surface of a plate-like inorganic pigment powder often used in cosmetics that can provide a smooth feel as described above. This has the effect of obtaining an extremely high ultraviolet absorption performance without losing the smooth feel of the device.
【0009】また、本発明においては、前記化粧料用顔
料粉体が球状の顔料粉体であるのが好ましい。このよう
に通常の化粧料に多く用いられる球状の顔料粉体の表面
に有機系紫外線吸収性化合物を分子レベルで分散包含被
覆処理させることにより、有機系紫外線吸収性化合物自
体の紫外線吸収性能を最大限に発揮させることができる
とともに、表面活性が低くされる。したがって、化粧料
に配合した場合であっても、感触がよく優れた日焼け防
止効果を得ることができ、有機系紫外線吸収性化合物が
顔料粉体の外部に溶出しにくいため、他の有機物質の変
質および皮脂への吸収を防止でき、肌への影響が少なく
安全性が高いという効果を奏する。In the present invention, the cosmetic pigment powder is preferably a spherical pigment powder. In this way, the surface of the spherical pigment powder often used in ordinary cosmetics is dispersed and covered with the organic ultraviolet absorbing compound at the molecular level to maximize the ultraviolet absorbing performance of the organic ultraviolet absorbing compound itself. And the surface activity is reduced. Therefore, even when blended in cosmetics, it is possible to obtain an excellent sunscreen effect with a good feel and because the organic ultraviolet absorbing compound is less likely to elute outside the pigment powder, Deterioration and absorption into sebum can be prevented, and there is an effect that the effect on the skin is small and the safety is high.
【0010】本発明における化粧料は、上述のような化
粧料用紫外線吸収性顔料を配合してなることを特徴とす
るものである。[0010] The cosmetic of the present invention is characterized by comprising the above-mentioned ultraviolet absorbing pigment for cosmetics.
【0011】本発明によれば、配合される化粧料用紫外
線吸収性顔料自体が分散性に優れているため、この化粧
料用紫外線吸収性顔料を配合してなる化粧料は、それら
化粧料用紫外線吸収性顔料となる化粧料用顔料粉体およ
び有機系紫外線吸収性化合物をそのまま配合してなる化
粧料に比べて、有機系紫外線吸収性化合物を分子状態で
均一に分散できるため分散性が高くなり、紫外線吸収性
能を最大限に発揮することができる効果を奏する。さら
に、前記有機系紫外線吸収性化合物が直接皮脂に触れる
ことがないため、肌への影響が少なく安全性が高いとい
う効果を奏する。According to the present invention, since the ultraviolet absorbing pigment for cosmetics to be blended itself has excellent dispersibility, the cosmetics containing the ultraviolet absorbing pigment for cosmetics can be used for such cosmetics. Higher dispersibility because the organic UV-absorbing compound can be uniformly dispersed in the molecular state, compared to a cosmetic pigment that is a mixture of a pigment powder for a cosmetic that becomes an UV-absorbing pigment and an organic UV-absorbing compound as it is. This has the effect of maximizing ultraviolet absorption performance. Furthermore, since the organic ultraviolet absorbing compound does not directly touch the sebum, it has an effect of little influence on the skin and high safety.
【0012】[0012]
【発明の実施の形態】本発明による化粧料用紫外線吸収
性顔料において、母体となる化粧料用顔料粉体としては
酸化チタン,シリカ,炭酸カルシウム,酸化亜鉛,酸化
アルミニウム,酸化マグネシウム,酸化ジルコニウム,
ケイ酸マグネシウム,硫酸バリウム,ベンガラ,黄色酸
化鉄,群青等が挙げられ、特に板状の無機顔料粉体とし
てはマイカ,セリサイト,タルク,カオリン,チタン被
覆雲母,窒化ホウ素等が挙げられる。また、球状の顔料
粉体としては、球状シリカ,ナイロンパウダー,球状シ
リコン樹脂粉体等が挙げられる。BEST MODE FOR CARRYING OUT THE INVENTION In the ultraviolet absorbing pigment for cosmetics according to the present invention, titanium oxide, silica, calcium carbonate, zinc oxide, aluminum oxide, magnesium oxide, zirconium oxide,
Examples thereof include magnesium silicate, barium sulfate, red iron oxide, yellow iron oxide, and ultramarine blue. In particular, examples of plate-like inorganic pigment powders include mica, sericite, talc, kaolin, titanium-coated mica, and boron nitride. Examples of the spherical pigment powder include spherical silica, nylon powder, and spherical silicon resin powder.
【0013】前記媒体となる有機高分子化合物として
は、適当な溶剤に容易に溶解させることができるよう
な、例えばポリメチルメタクリレート樹脂,アクリルシ
リコン共重合体樹脂,ポリカーボネート樹脂,ポリスチ
レン樹脂,非晶性ポリアリレート樹脂等が挙げられる。The organic high molecular compound serving as the medium is, for example, a polymethyl methacrylate resin, an acrylic silicon copolymer resin, a polycarbonate resin, a polystyrene resin, an amorphous resin which can be easily dissolved in an appropriate solvent. Polyarylate resin and the like can be mentioned.
【0014】前記化粧料用顔料粉体に包含被覆される有
機系紫外線吸収性化合物としては、ベンゾフェノン系と
して、2−ハイドロキシ−4−メトキシベンゾフェノ
ン,2−ハイドロキシ−4−メトキシベンゾフェノン−
5−スルホン酸,2−ハイドロキシ−4−メトキシベン
ゾフェノン−5−スルホン酸ナトリウム,2,2’−ジ
ハイドロキシ−4,4’−ジメトキシベンゾフェノン,
2,2’−ジハイドロキシ−4,4’−ジメトキシベン
ゾフェノン−5−スルホン酸ナトリウム,2,4−ジハ
イドロキシベンゾフェノン,2,2’,4,4’−テト
ラハイドロキシベンゾフェノンが挙げられ、パラアミノ
安息香酸系として、パラアミノ安息香酸,パラアミノ安
息香酸エチル,パラアミノ安息香酸グリセリル,パラジ
メチルアミノ安息香酸アミル,パラジハイドロキシプロ
ピル安息香酸エチル等が挙げられ、ケイ皮酸系として、
p−メトキシケイ皮酸−2−エチルヘキシル,4−メト
キシケイ皮酸−2−エトキシエチル等が挙げられ、サリ
チル酸系として、サリチル酸−2−エチルヘキシル,サ
リチル酸フェニル,サリチル酸ホモメチル等が挙げら
れ、その他のものとして2−(2−ハイドロキシ−5−
メチルフェニル)ベンゾトリアゾール,4−tert−
ブチル−4’−メトキシ−ベンゾイルメタン,ウロカニ
ン酸,ウロカニン酸エチル,ジメトキシベンジリデンジ
オキソイミダゾリジンプロピオン酸−2−エチルヘキシ
ル等が挙げられる。これら有機系紫外線吸収性化合物は
種類によって吸収波長領域が異なるため、要望に応じて
選択し、場合によっては2種以上を組み合わせるように
してもよい。The organic ultraviolet absorbing compound contained and coated in the cosmetic pigment powder includes 2-hydroxy-4-methoxybenzophenone and 2-hydroxy-4-methoxybenzophenone as benzophenones.
5-sulfonic acid, 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid sodium salt, 2,2′-dihydroxy-4,4′-dimethoxybenzophenone,
Sodium 2,2'-dihydroxy-4,4'-dimethoxybenzophenone-5-sulfonate, 2,4-dihydroxybenzophenone, 2,2 ', 4,4'-tetrahydroxybenzophenone, and para-aminobenzoic acid Examples of the system include paraaminobenzoic acid, ethyl paraaminobenzoate, glyceryl paraaminobenzoate, amyl paradimethylaminobenzoate, ethyl paradihydroxypropylbenzoate, and the like.
2-ethylhexyl p-methoxycinnamate, 2-ethoxyethyl 4-methoxycinnamate, and the like, and salicylic acids include 2-ethylhexyl salicylate, phenyl salicylate, homomethyl salicylate, and others. As 2- (2-hydroxy-5-
Methylphenyl) benzotriazole, 4-tert-
Butyl-4'-methoxy-benzoylmethane, urocanic acid, ethyl urocanate, 2-ethylhexyl dimethoxybenzylidene dioxoimidazolidinepropionate and the like. Since these organic UV-absorbing compounds have different absorption wavelength ranges depending on the type, they may be selected as required, and in some cases, two or more types may be combined.
【0015】前記有機高分子化合物を溶解させる適当な
溶媒としては、上記有機系紫外線吸収性化合物も同時に
溶解できることが必要となり、例えば塩化メチレン,四
塩化炭素,1,1,1−トリクロロエタン,イソプロピ
ルアルコール,酢酸ブチル等が挙げられる。As a suitable solvent for dissolving the organic polymer compound, it is necessary that the organic ultraviolet absorbing compound can be dissolved at the same time. For example, methylene chloride, carbon tetrachloride, 1,1,1-trichloroethane, isopropyl alcohol , Butyl acetate and the like.
【0016】また、本発明において、媒体となる有機高
分子化合物は、原料となる化粧料用顔料粉体に対して5
0重量%までが好ましく、さらに好ましくは30重量%
までである。この有機高分子化合物が前記化粧料用顔料
粉体に対して30重量%以上であると、有機高分子化合
物自体が析出して凝集塊を作り、または化粧料用顔料粉
体に包含被覆された場合であっても粒子同士が有機化合
物によって融着を起こして感触が悪くなる傾向が生じ始
め、50重量%以上であると顕著にこの状態が生じてし
まうからである。In the present invention, the organic polymer compound as a medium is added to the cosmetic pigment powder as a raw material in an amount of 5%.
Preferably up to 0% by weight, more preferably 30% by weight
Up to. When the amount of the organic polymer compound is 30% by weight or more with respect to the cosmetic pigment powder, the organic polymer compound itself precipitates to form an agglomerate, or is covered by the cosmetic pigment powder. This is because, even in this case, the particles tend to fuse with each other due to the organic compound and tend to have a poor feel, and when the content is 50% by weight or more, this state is remarkably caused.
【0017】また、前記有機系紫外線吸収性化合物は、
原料となる化粧料用顔料粉体に対して50重量%までが
好ましく、さらに好ましくは20重量%である。この有
機系紫外線吸収性化合物が、原料となる化粧料用顔料粉
体に対して20重量%を越えると、媒体である有機高分
子化合物の中に完全に包含されることが難しくなり、5
0重量%を越えると完全に包含されずに被覆している有
機高分子化合物の外側に存在するようになるためであ
る。Further, the organic ultraviolet absorbing compound is
It is preferably up to 50% by weight, more preferably 20% by weight, based on the cosmetic pigment powder as a raw material. When the amount of the organic ultraviolet absorbing compound exceeds 20% by weight based on the amount of the cosmetic pigment powder as a raw material, it is difficult to completely include the organic ultraviolet absorbing compound in the organic polymer compound as a medium.
If it exceeds 0% by weight, it will not be completely contained and will be present outside the coating organic polymer compound.
【0018】本発明による化粧料用紫外線吸収性顔料の
製造方法は、媒体となる有機高分子化合物を適当な溶媒
に1〜10重量%となるように溶解させ、その中に原料
となる化粧料用顔料粉体に対して望まれる紫外線吸収性
能となるように有機系紫外線吸収性化合物を同時に溶解
させる。この中に原料となる化粧料用顔料粉体を目的と
する包含被覆処理量となるように分散させる。このと
き、前記有機高分子化合物と有機系紫外線吸収性化合物
とを溶解させた溶液の体積と、原料となる化粧料用顔料
粉体の嵩とが等しくなるようにする。次いで、前記分散
溶液を一定時間撹拌させ、撹拌中に加熱あるいは減圧す
ることによって溶液を完全に蒸発させる。完全に蒸発さ
せた後、必要に応じて粉砕し、目的とする化粧料用紫外
線吸収性顔料が得られる。In the method for producing an ultraviolet absorbing pigment for cosmetics according to the present invention, an organic polymer compound as a medium is dissolved in an appropriate solvent so as to have a concentration of 1 to 10% by weight, and a cosmetic as a raw material is dissolved therein. The organic UV absorbing compound is simultaneously dissolved so as to have the desired UV absorbing performance for the pigment powder for use. The pigment powder for cosmetics, which is a raw material, is dispersed therein so as to have a target covering treatment amount. At this time, the volume of the solution in which the organic polymer compound and the organic ultraviolet absorbing compound are dissolved is equal to the bulk of the cosmetic pigment powder as a raw material. Next, the dispersion solution is stirred for a certain period of time, and the solution is completely evaporated by heating or reducing the pressure during the stirring. After being completely evaporated, it is pulverized, if necessary, to obtain the desired ultraviolet absorbing pigment for cosmetics.
【0019】また、別の製造方法としては、有機高分子
化合物と有機系紫外線吸収性化合物とを同時に溶解させ
た溶液中に、原料となる化粧料用顔料粉体を目的とする
包含被覆処理量となるように分散させてスラリー溶液を
作成する。このスラリー溶液をスプレードライ法によっ
て噴霧して瞬時に溶剤を蒸発させることにより、目的と
する化粧料用紫外線吸収性顔料が得られる。In another production method, a pigment powder for cosmetics as a raw material is contained in a solution obtained by simultaneously dissolving an organic polymer compound and an organic ultraviolet absorbing compound. To prepare a slurry solution. By spraying the slurry solution by a spray drying method and instantaneously evaporating the solvent, a desired ultraviolet absorbing pigment for cosmetics can be obtained.
【0020】このようにして得られた化粧料用紫外線吸
収性顔料は、原料となる化粧料用顔料粉体に、有機系紫
外線吸収性化合物が分子レベルで分散包含された有機高
分子化合物を媒体として被覆されているため、優れた分
散性を有して感触に優れ、表面活性が非常に低く、紫外
線吸収性能が非常に高いという効果を奏する。The ultraviolet absorbing pigment for cosmetics obtained in this manner is obtained by using an organic polymer compound in which an organic ultraviolet absorbing compound is dispersed and contained at the molecular level in a pigment powder for cosmetics as a raw material. As a result, it has excellent dispersibility, excellent feel, very low surface activity, and very high ultraviolet absorption performance.
【0021】本発明による化粧料用紫外線吸収性顔料
は、例えばシリコン処理,パーフルオロアルキルジ(オ
キエチル)アミンリン酸エステル処理(特公平5−86
984号公報に開示),金属セッケン処理,N−ラウロ
イル−L−リジン処理等の表面処理を施してもよい。The ultraviolet absorbing pigment for cosmetics according to the present invention can be, for example, treated with silicon, treated with perfluoroalkyldi (oxyethyl) amine phosphate (Japanese Patent Publication No. 5-86).
No. 984), surface treatment such as metal soap treatment and N-lauroyl-L-lysine treatment.
【0022】前記化粧料用紫外線吸収性顔料を配合して
なる化粧料においては、その化粧料用紫外線吸収性顔料
以外に通常に用いられる油剤,粉体(顔料,色素,樹
脂),フッ素化合物,樹脂,界面活性剤,粘剤,防腐
剤,香料,保湿材,生理活性成分,塩類,溶媒,キレー
ト剤,中和剤,pH調整剤等の成分を同時に配合するこ
とができる。In cosmetics containing the ultraviolet absorbing pigment for cosmetics, oils, powders (pigments, pigments, resins), fluorine compounds, fluorine compounds, and the like usually used in addition to the ultraviolet absorbing pigment for cosmetics are used. Components such as a resin, a surfactant, a viscosity agent, a preservative, a fragrance, a humectant, a physiologically active component, a salt, a solvent, a chelating agent, a neutralizing agent, and a pH adjuster can be simultaneously added.
【0023】前記粉体としては、例えば赤色104号,
赤色201号,黄色4号,青色1号,黒色401号等の
色素、黄色4号アルミニウムレーキ,黄色203号バリ
ウムレーキ等のレーキ色素、ナイロンパウダー,シルク
パウダー,ウレタンパウダー,テフロンパウダー,シリ
コンパウダー,セルロースパウダー,シリコンエラスト
マー等の高分子,黄酸化鉄,赤色酸化鉄,黒酸化鉄,酸
化クロム,カーボンブラック,群青,紺青等の有色顔
料、酸化チタン,酸化セリウム等の白色顔料、タルク,
マイカ,セリサイト,カオリン等の体質顔料、雲母チタ
ン等のパール顔料、硫酸バリウム,炭酸カルシウム,炭
酸マグネシウム,ケイ酸アルミニウム,ケイ酸マグネシ
ウム等の金属塩、シリカ,アルミナ等の無機粉体、微粒
子酸化チタン,微粒子酸化鉄,アルミナ処理微粒子酸化
チタン,シリカ処理微粒子酸化チタン,ベントナイト,
スメクタイト等が挙げられる。これら粉体の形状、大き
さに特に制限はない。As the powder, for example, Red No. 104,
Dyes such as Red No. 201, Yellow No. 4, Blue No. 1 and Black No. 401, lake dyes such as Yellow No. 4 aluminum lake and Yellow No. 203 barium lake, nylon powder, silk powder, urethane powder, Teflon powder, silicon powder, Polymers such as cellulose powder and silicone elastomer, yellow iron oxide, red iron oxide, black iron oxide, chromium oxide, carbon black, colored pigments such as ultramarine blue and dark blue, white pigments such as titanium oxide and cerium oxide, talc,
Extender pigments such as mica, sericite and kaolin, pearl pigments such as mica titanium, metal salts such as barium sulfate, calcium carbonate, magnesium carbonate, aluminum silicate and magnesium silicate, inorganic powders such as silica and alumina, and fine particle oxidation Titanium, fine particle iron oxide, alumina-treated fine particle titanium oxide, silica-treated fine particle titanium oxide, bentonite,
And smectite. The shape and size of these powders are not particularly limited.
【0024】前記油剤としては、例えばセチルアルコー
ル,イソステアリルアルコール,ラウリルアルコール,
ヘキサデシルアルコール,オクチルドデカノール等の高
級アルコール、イソステアリン酸,ウンデシレン酸,オ
レイン酸等の脂肪酸、グリセリン,ソルビトール,エチ
レングリコール,プロビレングリコール,ポリエチレン
グリコール等の多価アルコール、ミリスチン酸ミリスチ
ル,ラウリン酸ヘキシル,オレイン酸デシル,ミリスチ
ン酸イソプロピル,ジメチルオクタン酸ヘキシルデシ
ル,モノステアリン酸グリセリン,フタル酸ジエチル,
モノステアリン酸エチレングリコール,オキシステアリ
ン酸オクチル等のエステル類、流動パラフィン,ワセリ
ン,スクワラン等の炭化水素、ラノリン,還元ラノリ
ン,カルナバロウ等のロウ、ミンク油,カカオ油,ヤシ
油,バーム核油,ツバキ油,ゴマ油,ヒマシ油,オリー
ブ油等の油脂、エチレン・α−オレフィン・コオリゴマ
ー等が挙げられる。また、メチルハイドロジェンポリシ
ロキサン,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,ポリエーテル変性オルガノポリシロキサ
ン,フルオロアルキル・ポリオキシアルキレン共変性オ
ルガノポリシロキサン,アルキル変性オルガノポリシロ
キサン,末端変性オルガノポリシロキサン,フッ素変性
オルガノポリシロキサン,アモジメチコン,アミノ変性
オルガノポリシロキサン,シリコンゲル,アクリルシリ
コン,トリメチルシロキシケイ酸,シリコンRTVゴム
等のシリコン化合物、パーフルオロポリエーテル,フッ
化ピッチ,フルオロカーボン,フルオロアルコール,フ
ッ素化シリコンレジン等のフッ素化合物が挙げられる。Examples of the oil agent include cetyl alcohol, isostearyl alcohol, lauryl alcohol,
Higher alcohols such as hexadecyl alcohol and octyldodecanol; fatty acids such as isostearic acid, undecylenic acid and oleic acid; polyhydric alcohols such as glycerin, sorbitol, ethylene glycol, propylene glycol and polyethylene glycol; myristyl myristate; hexyl laurate Decyl oleate, isopropyl myristate, hexyldecyl dimethyloctanoate, glyceryl monostearate, diethyl phthalate,
Esters such as ethylene glycol monostearate and octyl oxystearate; hydrocarbons such as liquid paraffin, vaseline and squalane; waxes such as lanolin, reduced lanolin and carnauba wax; mink oil, cocoa oil, coconut oil, balm kernel oil, camellia And oils, sesame oil, castor oil, olive oil and the like, and ethylene / α-olefin / co-oligomer. Also, methyl hydrogen polysiloxane, dimethyl polysiloxane, methyl phenyl polysiloxane, polyether-modified organopolysiloxane, fluoroalkyl / polyoxyalkylene co-modified organopolysiloxane, alkyl-modified organopolysiloxane, terminal-modified organopolysiloxane, fluorine-modified Silicon compounds such as organopolysiloxane, amodimethicone, amino-modified organopolysiloxane, silicon gel, acrylic silicon, trimethylsiloxysilicic acid, silicon RTV rubber, perfluoropolyether, pitch fluoride, fluorocarbon, fluoroalcohol, fluorinated silicone resin And the like.
【0025】また、前記界面活性剤としては、例えばア
ニオン型界面活性剤,カチオン型界面活性剤,ノニオン
型界面活性剤,ベタイン型界面活性剤を用いることがで
きる。As the surfactant, for example, an anionic surfactant, a cationic surfactant, a nonionic surfactant, and a betaine surfactant can be used.
【0026】前記溶媒としては、精製水,エタノール,
軽質流動イソパラフィン,低級アルコール,エーテル
類,LPG,フルオロカーボン,N−メチルピロリド
ン,フルオロアルコール,パーフルオロポリエーテル,
代替フロン,揮発性シリコーン等が挙げられる。As the solvent, purified water, ethanol,
Light liquid isoparaffin, lower alcohol, ethers, LPG, fluorocarbon, N-methylpyrrolidone, fluoroalcohol, perfluoropolyether,
Alternative fluorocarbons, volatile silicones and the like can be mentioned.
【0027】前記化粧料複合顔料以外に前述のような油
剤等を配合してなる化粧料の具体例としては、例えばフ
ァンデーション,白粉,アイシャドウ,アイライナー,
チーク,口紅,ネイルカラー等のメイクアップ化粧料,
乳液,クリーム,ローション,カラミンローション,サ
ンスクリーン剤,サンタン剤,アフターシェープローシ
ョン,プレシェープローション,パック料,クレンジン
グ料,洗顔料,アクネ対策化粧料等の基礎化粧料,ヘア
カラー,ボディパウダー,デオドラント,石鹸,ボディ
シャンプー,入浴剤,香水等が挙げられる。Specific examples of cosmetics comprising the above-mentioned oils and the like in addition to the cosmetic composite pigments include, for example, foundations, white powders, eye shadows, eye liners,
Makeup cosmetics such as teak, lipstick, nail color,
Emulsions, creams, lotions, calamine lotions, sunscreens, suntans, after-shave lotions, pre-shape lotions, packs, cleansing ingredients, facial cleansers, basic cosmetics such as anti-acne cosmetics, hair colors, body powders, deodorants , Soaps, body shampoos, bath additives, perfumes and the like.
【0028】前述のような化粧料に配合される前記化粧
料用紫外線吸収性顔料の配合量としては、化粧料の総量
に対して0.1〜100重量%が好ましく、さらに好ま
しくは1〜60重量%である。また、紫外線防御成分の
配合量としては0.1〜50重量%が好ましく、抗酸化
剤の配合量としては0.001〜10重量%が好まし
い。The amount of the ultraviolet absorbing pigment for cosmetics to be blended in the above-mentioned cosmetics is preferably 0.1 to 100% by weight, more preferably 1 to 60% by weight, based on the total amount of the cosmetics. % By weight. Further, the compounding amount of the ultraviolet ray protection component is preferably 0.1 to 50% by weight, and the compounding amount of the antioxidant is preferably 0.001 to 10% by weight.
【0029】前記化粧料の剤型としては、二層状,油中
水型エマルション,水中油型エマルション,ジェル状,
スプレー,ムース状,油性,固型状等、従来公知の剤型
を使用することができる。特に、サンスクリーン剤の用
途には、二層状,油中水型エマルション,ジェル状が好
ましく、またファンデーションの用途には固型状,固型
エマルション状,ジェル状,油中水型エマルション,水
中油型エマルション,油性,ムース等が好ましい。Examples of the cosmetic formulation include two-layer, water-in-oil emulsion, oil-in-water emulsion, gel,
Conventionally known dosage forms such as spray, mousse, oily, and solid forms can be used. In particular, two-layer, water-in-oil emulsions and gels are preferred for sunscreen applications, and solid, solid emulsions, gels, water-in-oil emulsions and oil-in-water are preferred for foundation applications. Emulsions, oils, mousses and the like are preferred.
【0030】なお、本発明の化粧料用紫外線吸収性顔料
は、上述のような化粧料に限らず、例えば樹脂,塗料,
インキ,ガラス,繊維,紙等にも使用可能である。The UV-absorbing pigment for cosmetics of the present invention is not limited to the above-mentioned cosmetics, and may be, for example, resin, paint,
It can be used for ink, glass, fiber, paper, etc.
【0031】[0031]
【実施例】次に、本発明による化粧料用紫外線吸収性顔
料および化粧料の具体的製造実施例,実施例および比較
例について説明する。EXAMPLES Next, specific production examples, examples and comparative examples of the ultraviolet absorbing pigment for cosmetics and the cosmetic according to the present invention will be described.
【0032】(製造実施例1)ポリメチルメタクリレー
ト(数平均分子量50,000)2.5重量部を100
重量部のジクロロメタンに完全に溶解し、この溶液に
2.5重量部のp−メトキシケイ皮酸−2−エチルヘキ
シルを同時に溶解して50重量部のセリサイトを加えス
ラリーとする。このスラリー溶液をジャケット付(蒸気
加熱)真空ライン付のヘンシェルミキサーのような混合
撹拌乾燥機に投入して約30分間撹拌した後、約90℃
に加熱し、若干真空をかけて溶媒であるジクロロメタン
を完全に蒸発させる。その後、アトマイザーにて粉砕
し、セリサイトの表面にポリメチルメタクリレートを媒
体としてp−メトキシケイ皮酸−2−エチルヘキシルを
分子レベルで包含被覆させた化粧料用紫外線吸収性顔料
を得た。(Production Example 1) 2.5 parts by weight of polymethyl methacrylate (number average molecular weight 50,000) was added to 100 parts by weight.
It is completely dissolved in parts by weight of dichloromethane, and 2.5 parts by weight of 2-ethylhexyl p-methoxycinnamate is simultaneously dissolved in this solution, and 50 parts by weight of sericite is added to form a slurry. This slurry solution was put into a mixing / stirring dryer such as a Henschel mixer equipped with a jacketed (steam-heated) vacuum line and stirred for about 30 minutes.
And evaporate the solvent dichloromethane completely under a slight vacuum. Then, it was pulverized with an atomizer to obtain an ultraviolet-absorbing pigment for cosmetics in which p-methoxycinnamic acid-2-ethylhexyl was coated at the molecular level on the surface of sericite using polymethyl methacrylate as a medium.
【0033】(製造実施例2)下記化学構造式に示され
るアクリルシリコン共重合体5重量部を500重量部の
2−プロパノールに完全に溶解し、この溶液に2.5重
量部ずつの4−tert−ブチル−4’−メトキシベン
ゾイルメタンと、p−メトキシケイ皮酸−2−エチルヘ
キシルとを同時に溶解する。この溶液に50重量部のセ
リサイトを分散させてスラリーとする。このスラリーを
スプレー式ドライヤーで高圧噴霧して瞬時に2−プロパ
ノールを蒸発させることにより、セリサイト表面にアク
リルシリコン共重合体を媒体として4−tert−ブチ
ル−4’−メトキシベンゾイルメタンとp−メトキシケ
イ皮酸−2−エチルヘキシルとを分子レベルで包含被覆
させた化粧料用紫外線吸収性顔料を得た。(Production Example 2) 5 parts by weight of an acrylic silicone copolymer represented by the following chemical structural formula was completely dissolved in 500 parts by weight of 2-propanol, and 2.5 parts by weight of 4- Simultaneously dissolve tert-butyl-4'-methoxybenzoylmethane and 2-ethylhexyl p-methoxycinnamate. 50 parts by weight of sericite is dispersed in this solution to form a slurry. This slurry was sprayed with a spray drier under high pressure to instantaneously evaporate 2-propanol, thereby forming 4-tert-butyl-4'-methoxybenzoylmethane and p-methoxy on the sericite surface using an acrylic silicone copolymer as a medium. A UV-absorbing pigment for cosmetics was obtained, which was coated with 2-ethylhexyl cinnamate at the molecular level.
【化1】 Embedded image
【0034】(製造実施例3)前記製造実施例2に用い
られたものと同様のアクリルシリコン共重合体10重量
部を1000重量部の2−プロパノールに完全に溶解す
る。この溶液に5重量部ずつの4−tert−ブチル−
4’−メトキシベンゾイルメタンとp−メトキシケイ皮
酸−2−エチルヘキシルと同時に溶解する。この溶液に
50重量部の球状シリカ(平均粒子径8μm)を分散さ
せてスラリーとする。このスラリーを製造実施例2と同
様の方法にて、球状シリカ表面にアクリルシリコン共重
合体を媒体として4−tert−ブチル−4’−メトキ
シベンゾイルメタンとp−メトキシケイ皮酸−2−エチ
ルヘキシルとを分子レベルで包含被覆させた化粧料用紫
外線吸収性顔料を得た。(Production Example 3) 10 parts by weight of the same acrylic silicone copolymer as that used in Production Example 2 is completely dissolved in 1000 parts by weight of 2-propanol. 5 parts by weight of 4-tert-butyl-
Dissolves simultaneously with 4'-methoxybenzoylmethane and 2-ethylhexyl p-methoxycinnamate. 50 parts by weight of spherical silica (average particle diameter: 8 μm) is dispersed in this solution to form a slurry. This slurry was prepared in the same manner as in Production Example 2 by using 4-tert-butyl-4′-methoxybenzoylmethane and p-methoxycinnamic acid-2-ethylhexyl on the spherical silica surface using an acrylic silicone copolymer as a medium. At the molecular level to obtain an ultraviolet absorbing pigment for cosmetics.
【0035】(製造実施例4)ポリメチルメタクリレー
ト(数平均分子量50,000)2.5重量部を100
重量部のアセトンに完全に溶解する。この溶液に2.5
重量部のジメトキシベンジリデンオキソイミダゾリジン
プロピオン酸−2−エチルヘキシルを同時に溶解する。
この溶液に50重量部のタルクを分散させてスラリーと
する。このスラリー溶液を製造実施例1と同様の方法
で、タルク表面にポリメチルメタクリレートを媒体とし
てジメトキシベンジリデンオキソイミダゾリジンプロピ
オン酸−2−エチルヘキシルを分子レベルで包含被覆さ
せた化粧料用紫外線吸収性顔料を得た。(Production Example 4) 2.5 parts by weight of polymethyl methacrylate (number average molecular weight 50,000) was added to 100 parts by weight.
Dissolve completely in parts by weight of acetone. 2.5
The parts by weight of 2-methoxyhexyl dimethoxybenzylideneoxoimidazolidine propionate are simultaneously dissolved.
50 parts by weight of talc are dispersed in this solution to form a slurry. This slurry solution was treated in the same manner as in Production Example 1 with a UV-absorbing pigment for cosmetics in which talc surface was coated with 2-ethylhexyl dimethoxybenzylideneoxoimidazolidine propionate at the molecular level using polymethyl methacrylate as a medium. Obtained.
【0036】次に、前記製造実施例1〜4で調整された
紫外線吸収性顔料をそれぞれ実施例1〜4に使用して、
以下の配合にてファンデーションを調整した。Next, the ultraviolet-absorbing pigments prepared in Production Examples 1 to 4 were used in Examples 1 to 4, respectively.
The foundation was adjusted with the following composition.
【0037】 (実施例1,2) シリコン処理酸化チタン 10.0 製造実施例1または2(包含被覆セリサイト) 65.4 シリコン処理タルク 10.0 シリコン処理ベンガラ 0.3 シリコン処理黄酸化鉄 1.5 カーボンブラック 0.4 チタンブラック 0.4 メチルフェニルポリシロキサン 2.0 ジメチルポリシロキサン(6cs) 4.0 ジメチルポリシロキサン(20cs) 3.0 ジメチルポリシロキサン(10,000cs) 3.0 合計 100.0(Examples 1 and 2) Silicon-treated titanium oxide 10.0 Production Example 1 or 2 (inclusion coated sericite) 65.4 Silicon-treated talc 10.0 Silicon-treated Bengala 0.3 Silicon-treated iron oxide yellow 1 4.5 Carbon black 0.4 Titanium black 0.4 Methylphenyl polysiloxane 2.0 Dimethyl polysiloxane (6 cs) 4.0 Dimethyl polysiloxane (20 cs) 3.0 Dimethyl polysiloxane (10,000 cs) 3.0 Total 100 .0
【0038】 (実施例3) シリコン処理セリサイト 27.0 シリコン処理マイカ 12.5 シリコン処理タルク 38.7 シリコン処理酸化チタン 9.0 製造実施例3(包含被覆球状シリカ) 5.0 シリコン処理黄酸化鉄 2.0 シリコン処理ベンガラ 0.7 シリコン処理黒酸化鉄 0.3 ジメチルポリシロキサン(20cs) 4.8 合計 100.0(Example 3) Silicon-treated sericite 27.0 Silicon-treated mica 12.5 Silicon-treated talc 38.7 Silicon-treated titanium oxide 9.0 Production Example 3 (including coated spherical silica) 5.0 Silicon-treated yellow Iron oxide 2.0 Silicon-treated red iron oxide 0.7 Silicon-treated black iron oxide 0.3 Dimethylpolysiloxane (20cs) 4.8 Total 100.0
【0039】 (実施例4) シリコン処理酸化チタン 10.0 製造実施例1(包含被覆セリサイト) 65.4 製造実施例4(包含被覆タルク) 10.0 シリコン処理ベンガラ 0.3 シリコン処理黄酸化鉄 1.5 カーボンブラック 0.4 チタンブラック 0.4 メチルフェニルポリシロキサン 2.0 ジメチルポリシロキサン(6cs) 4.0 ジメチルポリシロキサン(20cs) 3.0 ジメチルポリシロキサン(10,000cs) 3.0 合計 100.0Example 4 Siliconized Titanium Oxide 10.0 Production Example 1 (Included Coated Sericite) 65.4 Production Example 4 (Included Coated Talc) 10.0 Siliconized Bengala 0.3 Siliconized Yellow Oxidation Iron 1.5 Carbon black 0.4 Titanium black 0.4 Methyl phenyl polysiloxane 2.0 Dimethyl polysiloxane (6 cs) 4.0 Dimethyl polysiloxane (20 cs) 3.0 Dimethyl polysiloxane (10,000 cs) 3.0 Total 100.0
【0040】次に、前記製造実施例1〜4で調整された
紫外線吸収性顔料の原料である有機紫外線吸収性化合物
をそれぞれそのまま比較例1〜4に使用し、前記実施例
1〜4に対応する配合となるように以下の配合にてファ
ンデーションを調整した。Next, the organic UV-absorbing compounds as raw materials of the UV-absorbing pigments prepared in the above-mentioned Production Examples 1 to 4 were used as they were in Comparative Examples 1 to 4, respectively. The foundation was adjusted with the following composition so as to obtain the desired composition.
【0041】 (比較例1) シリコン処理酸化チタン 10.0 シリコン処理セリサイト 62.4 シリコン処理タルク 10.0 シリコン処理ベンガラ 0.3 シリコン処理黄酸化鉄 1.5 カーボンブラック 0.4 チタンブラック 0.4 p−メトキシケイ皮酸−2−エチルヘキシル 3.0 メチルフェニルポリシロキサン 2.0 ジメチルポリシロキサン(6cs) 4.0 ジメチルポリシロキサン(20cs) 3.0 ジメチルポリシロキサン(10,000) 3.0 合計 100.0(Comparative Example 1) Silicon-treated titanium oxide 10.0 Silicon-treated sericite 62.4 Silicon-treated talc 10.0 Silicon-treated Bengala 0.3 Silicon-treated yellow iron oxide 1.5 Carbon black 0.4 Titanium black 0 2.4 p-methoxycinnamic acid-2-ethylhexyl 3.0 methylphenylpolysiloxane 2.0 dimethylpolysiloxane (6 cs) 4.0 dimethylpolysiloxane (20 cs) 3.0 dimethylpolysiloxane (10,000) 0 Total 100.0
【0042】 (比較例2) シリコン処理酸化チタン 10.0 シリコン処理セリサイト 60.0 シリコン処理タルク 10.0 シリコン処理ベンガラ 0.3 シリコン処理黄酸化鉄 1.5 カーボンブラック 0.4 チタンブラック 0.4 4−tert−ブチル−4’−メトキシベンゾイルメタン 2.7 p−メトキシケイ皮酸−2−エチルヘキシル 2.7 メチルフェニルポリシロキサン 2.0 ジメチルポリシロキサン(6cs) 4.0 ジメチルポリシロキサン(20cs) 3.0 ジメチルポリシロキサン(10,000) 3.0 合計 100.0(Comparative Example 2) Silicon-treated titanium oxide 10.0 Silicon-treated sericite 60.0 Silicon-treated talc 10.0 Silicon-treated Bengala 0.3 Silicon-treated yellow iron oxide 1.5 Carbon black 0.4 Titanium black 0 2.4 4-tert-butyl-4'-methoxybenzoylmethane 2.7 p-methoxycinnamic acid-2-ethylhexyl 2.7 methylphenylpolysiloxane 2.0 dimethylpolysiloxane (6cs) 4.0 dimethylpolysiloxane ( 20cs) 3.0 Dimethylpolysiloxane (10,000) 3.0 Total 100.0
【0043】 (比較例3) シリコン処理セリサイト 27.0 シリコン処理マイカ 12.5 シリコン処理タルク 38.7 シリコン処理酸化チタン 9.0 球状シリカ 4.3 シリコン処理黄酸化鉄 2.0 シリコン処理ベンガラ 0.7 シリコン処理黒酸化鉄 0.3 4−tert−ブチル−4’−メトキシベンゾイルメタン 0.35 p−メトキシケイ皮酸−2−エチルヘキシル 0.35 ジメチルポリシロキサン(20cs) 4.8 合計 100.0(Comparative Example 3) Silicon-treated sericite 27.0 Silicon-treated mica 12.5 Silicon-treated talc 38.7 Silicon-treated titanium oxide 9.0 Spherical silica 4.3 Silicon-treated yellow iron oxide 2.0 Silicon-treated red iron oxide 0.7 silicon-treated black iron oxide 0.3 4-tert-butyl-4′-methoxybenzoylmethane 0.35 p-methoxycinnamic acid-2-ethylhexyl 0.35 dimethylpolysiloxane (20 cs) 4.8 total 100 .0
【0044】 (比較例4) シリコン処理酸化チタン 10.0 シリコン処理セリサイト 62.4 シリコン処理タルク 10.0 シリコン処理ベンガラ 0.3 シリコン処理黄酸化鉄 1.5 カーボンブラック 0.4 チタンブラック 0.4 ジメトキシベンジリデンオキソイミダゾリンジプロピオン酸−2−エチルヘキシ ル 3.0 メチルフェニルポリシロキサン 2.0 ジメチルポリシロキサン(6cs) 4.0 ジメチルポリシロキサン(20cs) 3.0 ジメチルポリシロキサン(10,000) 3.0 合計 100.0(Comparative Example 4) Silicon-treated titanium oxide 10.0 Silicon-treated sericite 62.4 Silicon-treated talc 10.0 Silicon-treated Bengala 0.3 Silicon-treated yellow iron oxide 1.5 Carbon black 0.4 Titanium black 0 2.4 dimethoxybenzylideneoxoimidazolinediethylpropionate-2-ethylhexyl 3.0 methylphenylpolysiloxane 2.0 dimethylpolysiloxane (6 cs) 4.0 dimethylpolysiloxane (20 cs) 3.0 dimethylpolysiloxane (10,000) 3.0 Total 100.0
【0045】これら製造実施例1〜4,実施例1〜4お
よび比較例1〜4で得られた化粧料用紫外線吸収性顔料
もしくはファンデーションの紫外線吸収性能を測定し
た。前記化粧料用紫外線吸収性顔料もしくはファンデー
ションをスコッチテープ(3M社製)の接着面にそれぞ
れ均一に塗布して(塗布面積は15mm×25mm)、
その後重量を測定する。次いで、何も塗布されていない
スコッチテープをリファレンス側に置いて、日本分光社
製分光光度計U−bestU−570型にて波長範囲2
90〜450μmで吸収特性を測定し、得られた値を測
定部分領域での重量および面積で割ることにより定量的
に吸収性能を算出する。なお、このように測定された吸
収性能は規格化吸光度と呼ばれ、単位はabs/g/m
m2である。The ultraviolet absorbing performance of the ultraviolet absorbing pigments or foundations for cosmetics obtained in Production Examples 1-4, Examples 1-4 and Comparative Examples 1-4 was measured. The UV-absorbing pigment or foundation for cosmetics is uniformly applied to the adhesive surface of a scotch tape (manufactured by 3M) (application area is 15 mm × 25 mm),
Thereafter, the weight is measured. Then, a scotch tape on which nothing was applied was placed on the reference side, and a wavelength range of 2 was measured using a spectrophotometer U-bestU-570 manufactured by JASCO Corporation.
The absorption characteristics are measured at 90 to 450 μm, and the absorption performance is quantitatively calculated by dividing the obtained value by the weight and area in the measurement partial region. The absorption performance measured in this way is called a normalized absorbance, and the unit is abs / g / m
a m 2.
【0046】図1に製造実施例1〜4にて製造された化
粧料用紫外線吸収性顔料の紫外線吸収性能が、図2に実
施例1〜4にてファンデーションとして混合された粉体
の紫外線吸収性能が、図3に比較例1〜4にてファンデ
ーションとして混合された粉体の紫外線吸収性能がそれ
ぞれ示されている。また、表1には、製造実施例1〜
4,実施例1〜4および比較例1〜4における320n
m,360nmでの規格化吸光度の値が示されている。FIG. 1 shows the ultraviolet absorption performance of the ultraviolet absorbing pigments for cosmetics manufactured in Production Examples 1-4, and FIG. 2 shows the ultraviolet absorption of the powder mixed as a foundation in Examples 1-4. FIG. 3 shows the ultraviolet absorption performance of the powders mixed as foundations in Comparative Examples 1 to 4, respectively. Further, Table 1 shows Production Examples 1 to
4, 320n in Examples 1-4 and Comparative Examples 1-4
m, the value of the normalized absorbance at 360 nm is shown.
【0047】[0047]
【表1】 [Table 1]
【0048】図1に示されるように、製造実施例1は日
焼けの原因となる波長約300〜330nmの範囲で高
い規格化吸光度を有し、製造実施例2および3は日焼け
の原因となる波長約300〜330nmの範囲および皮
膚ガンの原因となる波長約330〜365nmの範囲で
高い規格化吸光度を有し、製造実施例4は皮膚ガンの原
因となる波長約330〜365nmの範囲で高い規格化
吸光度を有しているのが明らかである。As shown in FIG. 1, Production Example 1 has a high normalized absorbance in the wavelength range of about 300 to 330 nm which causes sunburn, and Production Examples 2 and 3 show wavelengths which cause sunburn. Manufacturing Example 4 has a high standardized absorbance in the range of about 300 to 330 nm and the wavelength of about 330 to 365 nm that causes skin cancer, and Production Example 4 has a high standardized absorbance in the range of about 330 to 365 nm that causes skin cancer. It is clear that the compound has an optical absorption.
【0049】図2および図3に示されるように、実施例
1は対応する比較例1に比べて日焼けの原因となる波長
約300〜330nmの範囲で高い規格化吸光度を有し
ており、実施例2および3は対応する比較例2および3
に比べて日焼けの原因となる波長約300〜330nm
の範囲および皮膚ガンの原因となる波長約330〜36
5nmの範囲で高い規格化吸光度を有し、実施例4は対
応する比較例4に比べて皮膚ガンの原因となる波長約3
30〜365nmの範囲で高い規格化吸光度を有してい
るのが明らかである。As shown in FIGS. 2 and 3, Example 1 has a higher normalized absorbance in the wavelength range of about 300 to 330 nm which causes sunburn than the corresponding Comparative Example 1. Examples 2 and 3 correspond to the corresponding comparative examples 2 and 3.
Approximately 300-330nm wavelength that causes sunburn compared to
Range and wavelengths of about 330-36 that cause skin cancer
Example 4 has a high normalized absorbance in the range of 5 nm, and Example 4 has a wavelength of about 3
It is clear that it has a high normalized absorbance in the range of 30 to 365 nm.
【0050】また、前記実施例1〜4で得られたファン
デーションを10人のパネラーが真夏の炎天下で使用し
たところ、対応する比較例1〜4のファンデーションに
比べて優れた日焼け防止効果が得られた。When the foundations obtained in Examples 1 to 4 were used by a panel of 10 people under the hot summer sun, a superior sunburn preventing effect was obtained as compared with the corresponding foundations of Comparative Examples 1 to 4. Was.
【0051】前述のように製造実施例1〜4の化粧料用
紫外線吸収性顔料は、有機化合物が分子レベルで分散存
在しているため、表面活性が低く優れた紫外線吸収性能
を有する効果を奏している。さらに、これら化粧料用紫
外線吸収性顔料を配合する化粧料は、それら化粧料用紫
外線吸収性顔料の原料である化粧料用顔料粉体および有
機系紫外線吸収性化合物をそのまま配合するのに比べて
非常に優れた紫外線吸収性能を有し、優れた日焼け防止
効果が得られる効果を奏する。As described above, the UV-absorbing pigments for cosmetics of Production Examples 1 to 4 exhibit an effect of having a low surface activity and excellent UV-absorbing performance because the organic compound is dispersed at the molecular level. ing. Furthermore, the cosmetics containing these UV absorbing pigments for cosmetics are more incomparable than the raw materials of the UV absorbing pigments for cosmetics, which are the raw materials of the pigments for cosmetics and the organic UV absorbing compounds. It has an extremely excellent ultraviolet absorbing performance and has an effect of obtaining an excellent sun protection effect.
【図1】図1は、製造実施例1〜4にて製造された化粧
料用紫外線吸収性顔料の紫外線吸収性能を表すグラフで
ある。FIG. 1 is a graph showing the ultraviolet absorbing performance of the ultraviolet absorbing pigment for cosmetics manufactured in Production Examples 1 to 4.
【図2】図2は、実施例1〜4にてファンデーションと
して混合された粉体の紫外線吸収性能を表すグラフであ
る。FIG. 2 is a graph showing the ultraviolet absorption performance of powder mixed as a foundation in Examples 1 to 4.
【図3】図3は、比較例1〜4にてファンデーションと
して混合された粉体の紫外線吸収性能を表すグラフであ
る。FIG. 3 is a graph showing the ultraviolet absorption performance of powders mixed as foundations in Comparative Examples 1 to 4.
Claims (4)
を媒体として有機系紫外線吸収性化合物を包含被覆させ
ることを特徴とする化粧料用紫外線吸収性顔料。1. An ultraviolet-absorbing pigment for cosmetics, wherein the pigment powder for cosmetics is coated with an organic ultraviolet-absorbing compound by using an organic polymer compound as a medium.
粉体である請求項1に記載の化粧料用紫外線吸収性顔
料。2. The ultraviolet absorbing pigment for cosmetics according to claim 1, wherein the cosmetic pigment powder is a plate-like inorganic pigment powder.
である請求項1に記載の化粧料用紫外線吸収性顔料。3. The ultraviolet absorbing pigment for cosmetics according to claim 1, wherein the cosmetic pigment powder is a spherical pigment powder.
の化粧料用紫外線吸収性顔料を配合してなることを特徴
とする化粧料。4. A cosmetic comprising the ultraviolet absorbent pigment for cosmetics according to claim 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10249390A JP2000080021A (en) | 1998-09-03 | 1998-09-03 | Ultraviolet absorbing pigment for cosmetic and cosmetic |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10249390A JP2000080021A (en) | 1998-09-03 | 1998-09-03 | Ultraviolet absorbing pigment for cosmetic and cosmetic |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2000080021A true JP2000080021A (en) | 2000-03-21 |
Family
ID=17192295
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10249390A Withdrawn JP2000080021A (en) | 1998-09-03 | 1998-09-03 | Ultraviolet absorbing pigment for cosmetic and cosmetic |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2000080021A (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1270686A2 (en) | 2001-06-12 | 2003-01-02 | Toda Kogyo Corporation | Organic and inorganic composite pigments, and paint and resin composition using the same |
| JP2013500942A (en) * | 2009-08-04 | 2013-01-10 | ロレアル | Composite pigment and preparation method thereof |
| JP2013501079A (en) * | 2009-08-04 | 2013-01-10 | ロレアル | Composite pigment and preparation method thereof |
| JP2013501078A (en) * | 2009-08-04 | 2013-01-10 | ロレアル | Composite pigment and preparation method thereof |
| JP2013018765A (en) * | 2011-06-16 | 2013-01-31 | Pola Chemical Industries Inc | Powder cosmetic |
| JP2014511397A (en) * | 2011-02-04 | 2014-05-15 | ロレアル | Composite pigment and preparation method |
| JP2014522375A (en) * | 2011-03-03 | 2014-09-04 | ウィシス テクノロジー ファウンデーション,インコーポレイティド | Thermodynamic solutions of metal oxides, metal chalcogenides, mixed metal oxides, and chalcogenides |
| US11266584B2 (en) | 2012-07-13 | 2022-03-08 | L'oreal | Cosmetic composition comprising composite sunscreen particles |
| US11523976B2 (en) | 2012-07-13 | 2022-12-13 | L'oreal | Composite pigment and method for preparing the same |
-
1998
- 1998-09-03 JP JP10249390A patent/JP2000080021A/en not_active Withdrawn
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1270686A2 (en) | 2001-06-12 | 2003-01-02 | Toda Kogyo Corporation | Organic and inorganic composite pigments, and paint and resin composition using the same |
| JP2013500942A (en) * | 2009-08-04 | 2013-01-10 | ロレアル | Composite pigment and preparation method thereof |
| JP2013501079A (en) * | 2009-08-04 | 2013-01-10 | ロレアル | Composite pigment and preparation method thereof |
| JP2013501078A (en) * | 2009-08-04 | 2013-01-10 | ロレアル | Composite pigment and preparation method thereof |
| JP2014511397A (en) * | 2011-02-04 | 2014-05-15 | ロレアル | Composite pigment and preparation method |
| JP2014522375A (en) * | 2011-03-03 | 2014-09-04 | ウィシス テクノロジー ファウンデーション,インコーポレイティド | Thermodynamic solutions of metal oxides, metal chalcogenides, mixed metal oxides, and chalcogenides |
| US10112156B2 (en) | 2011-03-03 | 2018-10-30 | Wisys Technology Foundation, Inc. | Thermodynamic solutions of metal chalcogenides and mixed metal oxides and chalcogenides |
| JP2013018765A (en) * | 2011-06-16 | 2013-01-31 | Pola Chemical Industries Inc | Powder cosmetic |
| US11266584B2 (en) | 2012-07-13 | 2022-03-08 | L'oreal | Cosmetic composition comprising composite sunscreen particles |
| US11523976B2 (en) | 2012-07-13 | 2022-12-13 | L'oreal | Composite pigment and method for preparing the same |
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| Date | Code | Title | Description |
|---|---|---|---|
| A300 | Withdrawal of application because of no request for examination |
Free format text: JAPANESE INTERMEDIATE CODE: A300 Effective date: 20060110 |