JPH10316526A - Powdered cosmetic material - Google Patents
Powdered cosmetic materialInfo
- Publication number
- JPH10316526A JPH10316526A JP14461197A JP14461197A JPH10316526A JP H10316526 A JPH10316526 A JP H10316526A JP 14461197 A JP14461197 A JP 14461197A JP 14461197 A JP14461197 A JP 14461197A JP H10316526 A JPH10316526 A JP H10316526A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- group
- embedded image
- represented
- silicone compound
- 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.)
- Pending
Links
- 239000002537 cosmetic Substances 0.000 title claims abstract description 20
- 239000000463 material Substances 0.000 title abstract description 5
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 20
- 150000001875 compounds Chemical class 0.000 claims abstract description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 5
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 4
- 239000000843 powder Substances 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 39
- 238000004519 manufacturing process Methods 0.000 description 12
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 8
- 238000010992 reflux Methods 0.000 description 8
- -1 methyl hydrogen Chemical compound 0.000 description 6
- 229910052697 platinum Inorganic materials 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 230000005923 long-lasting effect Effects 0.000 description 4
- 235000011056 potassium acetate Nutrition 0.000 description 4
- 229940105990 diglycerin Drugs 0.000 description 3
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920002545 silicone oil Polymers 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N ferrosoferric oxide Chemical compound O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- NPRYCHLHHVWLQZ-TURQNECASA-N 2-amino-9-[(2R,3S,4S,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-prop-2-ynylpurin-8-one Chemical compound NC1=NC=C2N(C(N(C2=N1)[C@@H]1O[C@@H]([C@H]([C@H]1O)F)CO)=O)CC#C NPRYCHLHHVWLQZ-TURQNECASA-N 0.000 description 1
- LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 1
- 240000002871 Tectona grandis Species 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- BTFJIXJJCSYFAL-UHFFFAOYSA-N arachidyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 230000000975 bioactive effect Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 125000001400 nonyl 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])C([H])([H])[H] 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
- 239000003921 oil Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Landscapes
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、親水性基としてポ
リグリセリンを有するポリグリセリン変性シリコーン化
合物を含有する粉末化粧料に関するものである。TECHNICAL FIELD The present invention relates to a powder cosmetic containing a polyglycerin-modified silicone compound having polyglycerin as a hydrophilic group.
【0002】[0002]
【従来の技術】シリコーン油は、その優れた伸展性、さ
っぱり感、安全性の高さから、化粧料を始め、広い分野
で使用されている。2. Description of the Related Art Silicone oils are used in a wide range of fields, including cosmetics, because of their excellent extensibility, freshness and high safety.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、シリコ
ーン油を化粧料に配合した場合、肌なじみが悪く、しっ
とり感に欠け、きしむ等官能的にマイナスとなる面もあ
った。従って、シリコーン油ののびの良さ、さっぱり感
等の官能の良さを持ちながら、しっとり感が高く、肌へ
の付着性に優れ、さらに化粧持ちの良くなる素材並びに
それを配合した化粧料の開発が望まれていた。However, when silicone oil is blended into cosmetics, there is also a problem that the skin does not fit well, lacks a moist feeling, and is negatively functional such as squeaking. Therefore, while having good organoleptic properties such as silicone oil's spreadability and refreshing feeling, the development of a material that has a high moist feeling, excellent adhesion to the skin, and a long-lasting makeup, and a cosmetic that incorporates it, has been developed. Was desired.
【0004】[0004]
【課題を解決するための手段】上記実情に鑑み、鋭意研
究した結果、ポリグリセリン変性シリコーン化合物を用
いることにより、肌への付着が良く、しっとりする等の
使用性に優れ、かつ、化粧持ちの非常に良い粉末化粧料
が得られることを見出だし、本発明を完成するに至っ
た。Means for Solving the Problems In view of the above circumstances, as a result of diligent research, the use of a polyglycerin-modified silicone compound has good adhesion to the skin, excellent usability such as moistness, and a long lasting makeup. It has been found that a very good powder cosmetic can be obtained, and the present invention has been completed.
【0005】すなわち本発明は、下記一般式(1)で示
される、ポリグリセリン変性シリコーン化合物を含有す
ることを特徴とする粉末化粧料に関するものである。That is, the present invention relates to a powder cosmetic containing a polyglycerin-modified silicone compound represented by the following general formula (1).
【0006】[0006]
【化5】 Embedded image
【0007】[式中、R1〜R10は同一又は異なっても
良く、炭素数1〜10のアルキル基、フェニル基を示
し、そのうち、少なくとも1つは下記式(A)、(B)
又は(C)[Wherein, R 1 to R 10 may be the same or different and represent an alkyl group having 1 to 10 carbon atoms or a phenyl group, at least one of which is represented by the following formulas (A) and (B)
Or (C)
【0008】[0008]
【化6】 Embedded image
【0009】[0009]
【化7】 Embedded image
【0010】[0010]
【化8】 Embedded image
【0011】(但し、Qは炭素数1〜10の2価炭化水
素基、lは2〜20、mは2〜20の正の整数であ
る。)で表わされる基を示し、p、qはそれぞれ0以上
の整数であるが、p=0、q≠0のときR1〜R3、R6
〜R10の少なくとも1つは上記式(A)、(B)又は
(C)で表わされる基を示し、p≠0、q=0のときR
1〜R5、R8〜R10の少なくとも1つは上記式(A)、
(B)又は(C)で表わされる基を示し、p=q=0の
ときR1〜R3、R8〜R10の少なくとも1つは上記式
(A)、(B)又は(C)で表わされる基を示す。]以
下、本発明について詳細に説明する。(Wherein Q is a divalent hydrocarbon group having 1 to 10 carbon atoms, l is a positive integer of 2 to 20, and m is a positive integer of 2 to 20), and p and q are Each is an integer of 0 or more, but when p = 0 and q ≠ 0, R 1 to R 3 and R 6
At least one of R 10 to R 10 represents a group represented by the above formula (A), (B) or (C), and when p ≠ 0 and q = 0,
At least one of 1 to R 5 and R 8 to R 10 is the above formula (A);
And a group represented by (B) or (C), and when p = q = 0, at least one of R 1 to R 3 and R 8 to R 10 is a group represented by the above formula (A), (B) or (C) Represents a group represented by Hereinafter, the present invention will be described in detail.
【0012】本発明で用いられるポリグリセリン変性シ
リコーン化合物は、上記一般式(1)に示すごとく、ポ
リグリセリンがスペーサーを介してシリコーン鎖に結合
した化合物である。上記一般式(1)で示される化合物
において、式中、R1〜R10は同一又は異なっても良
く、炭素数1〜10のアルキル基、フェニル基を示し、
例えば、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、デケル基、シクロペンチル基、シクロヘキシル
基、フェニル基、トリル基等が挙げられ、さらにR1〜
R10の少なくとも1つは上記式(A)、(B)又は
(C)で示される基であるが、ジグリセリン、トリグリ
セリン、テトラグリセリン等が挙げられる。The polyglycerin-modified silicone compound used in the present invention is a compound in which polyglycerin is bonded to a silicone chain via a spacer as shown in the general formula (1). In the compound represented by the general formula (1), R 1 to R 10 may be the same or different, and represent an alkyl group having 1 to 10 carbon atoms or a phenyl group;
For example, methyl group, ethyl group, propyl group, butyl group,
Pentyl group, a hexyl group, heptyl group, octyl group, nonyl group, Dekeru group, a cyclopentyl group, a cyclohexyl group, a phenyl group, a tolyl group and the like, further R 1 ~
At least one of R 10 is a group represented by the above formula (A), (B) or (C), and examples thereof include diglycerin, triglycerin, and tetraglycerin.
【0013】本発明のポリグリセリン変性シリコーン化
合物を粉末化粧料に配合する場合、化粧料に対して、
0.1〜20重量%(以下、単に「%」と記す)を配合
するのが好ましい。When the polyglycerin-modified silicone compound of the present invention is blended in a powder cosmetic,
It is preferable to add 0.1 to 20% by weight (hereinafter simply referred to as "%").
【0014】本発明において、粉末化粧料とは、白粉、
プレストパウダー、チークカラー、アイシャドウ等のメ
ークアップ化粧料、皮膚化粧料のみならず、外用医薬品
などの使用時に感触が問題とされる、皮膚に外用される
すべての粉末製品を包含する。In the present invention, the powder cosmetic is a white powder,
This includes not only makeup cosmetics such as prest powder, teak color, and eye shadow, and skin cosmetics, but also all powdered products that are applied externally to the skin, which have a problem in touch when used in external medicines.
【0015】本発明の粉末化粧料では、上記の成分に加
え、本発明の効果を妨げない範囲で通常の化粧料に使用
される固体、半固体、液状の油剤、水、水溶性高分子、
多価アルコール、溶剤、界面活性剤、粉体、樹脂、有機
変性粘土鉱物、高分子、紫外線吸収剤、保湿剤、防腐
剤、殺菌剤、香料、酸化防止剤、美肌用成分、生理活性
成分などを配合することができる。In the powder cosmetic of the present invention, in addition to the above-mentioned components, solid, semi-solid, liquid oils, water, water-soluble polymers,
Polyhydric alcohols, solvents, surfactants, powders, resins, organically modified clay minerals, polymers, UV absorbers, humectants, preservatives, bactericides, fragrances, antioxidants, skin care ingredients, bioactive ingredients, etc. Can be blended.
【0016】[0016]
【実施例】以下に、本発明を実施例を挙げて説明する
が、本発明は、これらの実施例によって限定されるもの
ではない。EXAMPLES The present invention will be described below with reference to examples, but the present invention is not limited to these examples.
【0017】製造例1 攪拌機、温度計及び還流冷却器を付したガラス製フラス
コに下記式のジグリセリンモノアリルエーテル100.
0g、Production Example 1 A diglycerin monoallyl ether of the following formula was placed in a glass flask equipped with a stirrer, thermometer and reflux condenser.
0 g,
【0018】[0018]
【化9】 Embedded image
【0019】及び下記式で表わされるメチルハイドロジ
ェンポリシロキサン248.7g、And 248.7 g of methyl hydrogen polysiloxane represented by the following formula:
【0020】[0020]
【化10】 Embedded image
【0021】イソプロピルアルコール200g、酢酸カ
リウムの10%エタノール溶液0.5g及び塩化白金酸
のイソプロピルアルコール溶液(白金濃度2%以上、以
下白金触媒と記載する)0.5gを仕込み、加熱してイ
ソプロピルアルコールの還流温度で3時間反応を行なっ
た。反応終了後、イソプロピルアルコールを減圧留去し
て、下記式のジグリセリン変性シリコーン化合物32
3.0gを得た。200 g of isopropyl alcohol, 0.5 g of a 10% ethanol solution of potassium acetate and 0.5 g of an isopropyl alcohol solution of chloroplatinic acid (platinum concentration: 2% or more, hereinafter referred to as a platinum catalyst) were charged, and heated to isopropyl alcohol. At reflux temperature for 3 hours. After completion of the reaction, isopropyl alcohol was distilled off under reduced pressure to obtain a diglycerin-modified silicone compound 32 represented by the following formula.
3.0 g were obtained.
【0022】[0022]
【化11】 Embedded image
【0023】製造例2 前記した製造例1と同様に、攪拌機、温度計及び還流冷
却器を付したガラス製フラスコに下記式のジグリセリン
モノアリルエーテル100.0g、Production Example 2 In the same manner as in Production Example 1 described above, 100.0 g of diglycerin monoallyl ether of the following formula was placed in a glass flask equipped with a stirrer, thermometer and reflux condenser.
【0024】[0024]
【化12】 Embedded image
【0025】及び製造例1で用いたメチルハイドロジェ
ンポリシロキサン248.7g、イソプロピルアルコー
ル200g、酢酸カリウムの10%エタノール溶液0.
5g及び白金触媒0.5gを仕込み、加熱してイソプロ
ピルアルコールの還流温度で3時間反応を行なった。反
応終了後、イソプロピルアルコールを減圧留去して、下
記式のジグリセリン変性シリコーン化合物323.0g
を得た。Further, 248.7 g of methyl hydrogen polysiloxane used in Production Example 1, 200 g of isopropyl alcohol, and a 10% ethanol solution of potassium acetate in 0.1% were used.
5 g and 0.5 g of a platinum catalyst were charged, heated and reacted at the reflux temperature of isopropyl alcohol for 3 hours. After completion of the reaction, isopropyl alcohol was distilled off under reduced pressure to obtain 323.0 g of a diglycerin-modified silicone compound represented by the following formula.
I got
【0026】[0026]
【化13】 Embedded image
【0027】製造例3 前記した製造例1と同様に、攪拌機、温度計及び還流冷
却器を付したガラス製フラスコに下記式のトリグリセリ
ンモノアリルエーテル50.0g、Production Example 3 In the same manner as in Production Example 1, 50.0 g of triglycerin monoallyl ether of the following formula was placed in a glass flask equipped with a stirrer, a thermometer and a reflux condenser.
【0028】[0028]
【化14】 Embedded image
【0029】及び下記式で表わされるメチルハイドロジ
ェンポリシロキサン323.2g、And 323.2 g of methyl hydrogen polysiloxane represented by the following formula:
【0030】[0030]
【化15】 Embedded image
【0031】イソプロピルアルコール200g、酢酸カ
リウムの10%エタノール溶液1.0g及び白金触媒
0.5gを仕込み、加熱し、イソプロピルアルコールの
還流温度で5時間反応を行なった。反応終了後、イソプ
ロピルアルコールを減圧留去して、下記式のトリグリセ
リン変性シリコーン化合物350.2gを得た。得られ
たトリグリセリン変性シリコーン化合物は、粘度が3.
7万cs(25℃)、屈折率1.4164(25℃)の
粘ちょうな液体であった。200 g of isopropyl alcohol, 1.0 g of a 10% ethanol solution of potassium acetate and 0.5 g of a platinum catalyst were charged, heated, and reacted at the reflux temperature of isopropyl alcohol for 5 hours. After completion of the reaction, isopropyl alcohol was distilled off under reduced pressure to obtain 350.2 g of a triglycerin-modified silicone compound represented by the following formula. The obtained triglycerin-modified silicone compound has a viscosity of 3.
It was a viscous liquid having a viscosity of 70,000 cs (25 ° C.) and a refractive index of 1.4164 (25 ° C.).
【0032】[0032]
【化16】 Embedded image
【0033】製造例4 前記した製造例1と同様に、攪拌機、温度計及び還流冷
却器を付したガラス製フラスコに下記式で表わされるメ
チルハイドロジェンポリシロキサン120.0g、Production Example 4 In the same manner as in Production Example 1 described above, 120.0 g of methylhydrogenpolysiloxane represented by the following formula was placed in a glass flask equipped with a stirrer, a thermometer and a reflux condenser.
【0034】[0034]
【化17】 Embedded image
【0035】及び製造例3で用いたトリグリセリンモノ
アリルエーテル154.0g、イソプロピルアルコール
120g、酢酸カリウムの10%エタノール溶液0.3
g及び白金触媒0.3gを仕込み、加熱してイソプロピ
ルアルコールの還流温度で5時間反応を行なった。反応
終了後、イソプロピルアルコールを減圧留去して、下記
式のトリグリセリン変性シリコーン化合物246.8g
を得た。And 154.0 g of triglycerin monoallyl ether, 120 g of isopropyl alcohol and 0.3% of a 10% ethanol solution of potassium acetate used in Production Example 3.
g of platinum catalyst and 0.3 g of platinum catalyst were heated and reacted at the reflux temperature of isopropyl alcohol for 5 hours. After completion of the reaction, isopropyl alcohol was distilled off under reduced pressure, and 246.8 g of a triglycerin-modified silicone compound represented by the following formula was obtained.
I got
【0036】[0036]
【化18】 Embedded image
【0037】実施例1及び比較例1 プレストパウダー
化粧料 次の表1に示す各組成のプレストパウダー化粧料を製造
し、その使用性について評価した。Example 1 and Comparative Example 1 Pressed Powder Cosmetic Pressed powder cosmetics having the respective compositions shown in Table 1 below were produced, and their usability was evaluated.
【0038】[0038]
【表1】 [Table 1]
【0039】(製造方法) A:成分1〜6を混合する。 B:成分7〜9を混合し、Aを加える。 C:Bに成分10を加えて金皿にプレス成型する(Production method) A: Components 1 to 6 are mixed. B: Components 7 to 9 are mixed, and A is added. C: Add component 10 to B and press mold into a metal plate
【0040】(評価)女性50名のパネルにより使用テ
ストを行ない、肌へののび、おさまりの良さ、べたつき
のなさ、しっとり感、仕上がりの美しさ、化粧持ちの良
さについて下記の基準で評価を行ない、その平均点で判
定した。(Evaluation) A use test was conducted by a panel of 50 women, and the following criteria were used to evaluate spreadability to the skin, good fit, no stickiness, moist feeling, beautiful finish, and good makeup. And the average score was used.
【0041】[評価基準] 5点:非常に良好 4点:良好 3点:普通 2点:やや不良 1点:不良 [判定] ◎:平均点4.5以上 ○:平均点3.5以上4.5未満 △:平均点2.5以上3.5未満 ×:平均点2.5未満 得られた結果を表2に示す。[Evaluation Criteria] 5 points: very good 4 points: good 3 points: normal 2 points: slightly poor 1 point: bad Less than 0.5 Δ: Average score of 2.5 or more and less than 3.5 ×: Average score of less than 2.5 The obtained results are shown in Table 2.
【0042】[0042]
【表2】 [Table 2]
【0043】表2の結果より明らかなように、本発明の
ポリグリセリン変性シリコーン化合物を配合した実施例
1のプレストパウダー化粧料は比較例1に比べ、肌への
のび、おさまりに優れ、べたつきがなくしっとりとし、
仕上がりも美しく、化粧持ちも非常に良いものであっ
た。As is clear from the results shown in Table 2, the pressed powder cosmetic of Example 1 in which the polyglycerin-modified silicone compound of the present invention was blended was superior to Comparative Example 1 in terms of spreading and relaxing on the skin and having a sticky property. Moist,
The finish was beautiful and the makeup lasted very well.
【0044】実施例2 パウダーファンデーション 次に示す組成のファンデーションを製造し、その使用性
について評価した。Example 2 Powder foundation A foundation having the following composition was produced and its usability was evaluated.
【0045】 (組成) (%) 1.ジメチルポリシロキサン 8.0 2.オクチルドデカノール 3.0 3.ポリグリセリン変性シリコーン化合物(製造例3) 1.5 4.防腐剤 適量 5 香料 適量 6.セリサイト 40.0 7.マイカ 10.0 8.タルク 残量 9.酸化チタン 10.0 10.微粒子酸化チタン 5.0 11.ステアリン酸マグネシウム 3.0 12.ベンガラ 0.9 13.黄酸化鉄 2.9 14.黒酸化鉄 0.4(Composition) (%) 1. Dimethyl polysiloxane 8.0 Octyldodecanol 3.0 3. Polyglycerin-modified silicone compound (Production Example 3) 1.5 4. Preservatives qs 5 flavors qs 6. Sericite 40.0 7. Mica 10.0 8. Talc balance 9. Titanium oxide 10.0 10. Fine particle titanium oxide 5.0 11. Magnesium stearate 3.0 12. Bengara 0.9 13. 2.9 Yellow iron oxide Black iron oxide 0.4
【0046】(製造方法) A:成分1〜5を混合する。 B:成分6〜14を混合し、Aを加え、均一に混合す
る。 C:Bを金皿にプレス成型する。 実施例2は、安定性に優れ、べたつきがなく、化粧持ち
の非常に良いファンデーションであった。(Production method) A: Components 1 to 5 are mixed. B: Components 6 to 14 are mixed, A is added and mixed uniformly. C: B is pressed into a metal plate. Example 2 was a foundation with excellent stability, no stickiness and a very long lasting makeup.
【0047】[0047]
【発明の効果】以上詳述したように、ポリグリセリン変
性シリコーン化合物を配合した粉末化粧料は、肌への付
着が良く、しっとりする等の使用性に優れ、化粧持ちの
非常に良いものである。As described in detail above, powder cosmetics containing a polyglycerin-modified silicone compound have good adhesion to the skin, excellent moistness and other usability, and have a very long lasting makeup. .
Claims (1)
セリン変性シリコーン化合物を含有することを特徴とす
る粉末化粧料。 【化1】 [式中、R1〜R10は同一又は異なっても良く、炭素数
1〜10のアルキル基、フェニル基を示し、そのうち、
少なくとも1つは下記式(A)、(B)又は(C) 【化2】 【化3】 【化4】 (但し、Qは炭素数1〜10の2価炭化水素基、lは2
〜20、mは2〜20の正の整数である。)で表わされ
る基を示し、p、qはそれぞれ0以上の整数であるが、
p=0、q≠0のときR1〜R3、R6〜R10の少なくと
も1つは上記式(A)、(B)又は(C)で表わされる
基を示し、p≠0、q=0のときR1〜R5、R8〜R10
の少なくとも1つは上記式(A)、(B)又は(C)で
表わされる基を示し、p=q=0のときR1〜R3、R8
〜R10の少なくとも1つは上記式(A)、(B)又は
(C)で表わされる基を示す。]1. A powder cosmetic comprising a polyglycerin-modified silicone compound represented by the following general formula (1). Embedded image [Wherein, R 1 to R 10 may be the same or different and represent an alkyl group having 1 to 10 carbon atoms or a phenyl group;
At least one is represented by the following formula (A), (B) or (C): Embedded image Embedded image (However, Q is a divalent hydrocarbon group having 1 to 10 carbon atoms, l is 2
-20 and m are positive integers of 2-20. ) Represents a group represented by p and q are each an integer of 0 or more,
When p = 0 and q ≠ 0, at least one of R 1 to R 3 and R 6 to R 10 represents a group represented by the above formula (A), (B) or (C), and p ≠ 0, q = R 1 to R 5 when 0, R 8 ~R 10
At least one represents a group represented by the above formula (A), (B) or (C), and when p = q = 0, R 1 to R 3 and R 8
At least one of R 10 represents a group represented by the above formula (A), (B) or (C). ]
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14461197A JPH10316526A (en) | 1997-05-19 | 1997-05-19 | Powdered cosmetic material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14461197A JPH10316526A (en) | 1997-05-19 | 1997-05-19 | Powdered cosmetic material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH10316526A true JPH10316526A (en) | 1998-12-02 |
Family
ID=15366061
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14461197A Pending JPH10316526A (en) | 1997-05-19 | 1997-05-19 | Powdered cosmetic material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH10316526A (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004339244A (en) * | 2002-03-25 | 2004-12-02 | Kao Corp | Branched polyglycerol-modified silicone |
| JP2008143838A (en) * | 2006-12-11 | 2008-06-26 | Pola Chem Ind Inc | Cosmetic containing surface-treated powder |
| US7655744B2 (en) | 2002-03-25 | 2010-02-02 | Kao Corporation | Branched polyglycerol-modified silicone |
| KR101047618B1 (en) * | 2007-11-14 | 2011-07-07 | (주)아모레퍼시픽 | Makeup cosmetic composition of granule particle type containing volatile silicone oil and polyglycerin modified silicone |
| US20110185947A1 (en) * | 2008-07-08 | 2011-08-04 | Byk-Chemie Gmbh | Polyhydroxyfunctional polysiloxane as anti-adhesive and dirt-repellant additives in coatings polymeric moulded masses and thermoplastics, method for production and use thereof |
| US20110294933A1 (en) * | 2008-07-08 | 2011-12-01 | Byk-Chemie Gmbh | Polyhydroxyfunctional polysiloxanes for increasing the surface energy of thermoplastics, method for production and use thereof |
| EP2581401A1 (en) | 2011-10-11 | 2013-04-17 | Shin-Etsu Chemical Co., Ltd. | Glycerol group-containing organopolysiloxane, cosmetic, and method for producing glycerol group-containing organopolysiloxane |
| WO2013103147A1 (en) | 2011-12-27 | 2013-07-11 | Dow Corning Toray Co., Ltd. | Diglycerin derivate-modified silicone, emulsifier for water-in-oil emulsion using the same, external use preparation, and cosmetic composition |
| WO2014104255A1 (en) * | 2012-12-28 | 2014-07-03 | 東レ・ダウコーニング株式会社 | High-purity monoalkenyl-containing glycerin derivative, and method for producing same |
| KR20140106745A (en) | 2011-12-27 | 2014-09-03 | 다우 코닝 도레이 캄파니 리미티드 | Co-modified organopolysiloxane, emulsifier for water-in-oil emulsion, external use preparation, and cosmetic composition using the same |
| EP2886161A1 (en) | 2013-12-12 | 2015-06-24 | Shin-Etsu Chemical Co., Ltd. | Cosmetic composition |
| CN104945628A (en) * | 2015-06-26 | 2015-09-30 | 中国日用化学工业研究院 | Polyglycerine modified organosilicon and method for preparing the same |
-
1997
- 1997-05-19 JP JP14461197A patent/JPH10316526A/en active Pending
Cited By (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7655744B2 (en) | 2002-03-25 | 2010-02-02 | Kao Corporation | Branched polyglycerol-modified silicone |
| JP2004339244A (en) * | 2002-03-25 | 2004-12-02 | Kao Corp | Branched polyglycerol-modified silicone |
| JP2008143838A (en) * | 2006-12-11 | 2008-06-26 | Pola Chem Ind Inc | Cosmetic containing surface-treated powder |
| KR101047618B1 (en) * | 2007-11-14 | 2011-07-07 | (주)아모레퍼시픽 | Makeup cosmetic composition of granule particle type containing volatile silicone oil and polyglycerin modified silicone |
| US8486188B2 (en) * | 2008-07-08 | 2013-07-16 | Byk-Chemie Gmbh | Polyhydroxyfunctional polysiloxane as anti-adhesive and dirt-repellant additives |
| US20110185947A1 (en) * | 2008-07-08 | 2011-08-04 | Byk-Chemie Gmbh | Polyhydroxyfunctional polysiloxane as anti-adhesive and dirt-repellant additives in coatings polymeric moulded masses and thermoplastics, method for production and use thereof |
| JP2011527350A (en) * | 2008-07-08 | 2011-10-27 | ベーイプシロンカー ヘミー ゲゼルシャフト ミット ベシュレンクター ハフトゥング | Polyhydroxyfunctional polysiloxanes as anti-stick and anti-fouling agents in paints, polymer molding materials and thermoplastics, their preparation and use |
| US20110294933A1 (en) * | 2008-07-08 | 2011-12-01 | Byk-Chemie Gmbh | Polyhydroxyfunctional polysiloxanes for increasing the surface energy of thermoplastics, method for production and use thereof |
| US8580241B2 (en) | 2011-10-11 | 2013-11-12 | Shin-Etsu Chemical Co., Ltd. | Glycerol group-containing organopolysiloxane, cosmetic, and method for producing glycerol group-containing organopolysiloxane |
| EP2581401A1 (en) | 2011-10-11 | 2013-04-17 | Shin-Etsu Chemical Co., Ltd. | Glycerol group-containing organopolysiloxane, cosmetic, and method for producing glycerol group-containing organopolysiloxane |
| US9480630B2 (en) | 2011-12-27 | 2016-11-01 | Dow Corning Toray Co., Ltd. | Co-modified organopolysiloxane, emulsifier for water-in-oil emulsion, external use preparation, and cosmetic composition using the same |
| KR20140106745A (en) | 2011-12-27 | 2014-09-03 | 다우 코닝 도레이 캄파니 리미티드 | Co-modified organopolysiloxane, emulsifier for water-in-oil emulsion, external use preparation, and cosmetic composition using the same |
| KR20140127231A (en) | 2011-12-27 | 2014-11-03 | 다우 코닝 도레이 캄파니 리미티드 | Diglycerin derivative-modified silicone, emulsifier for water-in-oil emulsion using the same, external use preparation, and cosmetic composition |
| WO2013103147A1 (en) | 2011-12-27 | 2013-07-11 | Dow Corning Toray Co., Ltd. | Diglycerin derivate-modified silicone, emulsifier for water-in-oil emulsion using the same, external use preparation, and cosmetic composition |
| US10085928B2 (en) | 2011-12-27 | 2018-10-02 | Dow Corning Toray Co., Ltd. | Diglycerin derivate-modified silicone, emulsifier for water-in-oil emulsion using the same, external use preparaton, and cosmetic composition |
| WO2014104255A1 (en) * | 2012-12-28 | 2014-07-03 | 東レ・ダウコーニング株式会社 | High-purity monoalkenyl-containing glycerin derivative, and method for producing same |
| CN105189430A (en) * | 2012-12-28 | 2015-12-23 | 道康宁东丽株式会社 | High-purity monoalkenyl-containing glycerin derivative, and method for producing same |
| US9663432B2 (en) | 2012-12-28 | 2017-05-30 | Dow Corning Toray Co., Ltd. | High-purity monoalkenyl-containing glycerin derivative and method of manufacturing same |
| CN105189430B (en) * | 2012-12-28 | 2018-08-10 | 道康宁东丽株式会社 | High-purity glycerol derivatives containing monoene and its manufacturing method |
| EP2886161A1 (en) | 2013-12-12 | 2015-06-24 | Shin-Etsu Chemical Co., Ltd. | Cosmetic composition |
| US9283165B2 (en) | 2013-12-12 | 2016-03-15 | Shin-Etsu Chemical Co., Ltd. | Cosmetic composition |
| CN104945628A (en) * | 2015-06-26 | 2015-09-30 | 中国日用化学工业研究院 | Polyglycerine modified organosilicon and method for preparing the same |
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