JPS6261911A - Makeup cosmetic - Google Patents
Makeup cosmeticInfo
- Publication number
- JPS6261911A JPS6261911A JP60203064A JP20306485A JPS6261911A JP S6261911 A JPS6261911 A JP S6261911A JP 60203064 A JP60203064 A JP 60203064A JP 20306485 A JP20306485 A JP 20306485A JP S6261911 A JPS6261911 A JP S6261911A
- Authority
- JP
- Japan
- Prior art keywords
- makeup
- plasticizer
- makeup cosmetic
- film
- volatile oil
- 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
Landscapes
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、新規なメイクアップ化粧料に関し、その目的
とするところは、落ちにくく、色移りがなく、使用感が
良く、かつ安全性の高いメイクアップ化粧料を提供する
ものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a new make-up cosmetic, which aims to be hard to remove, color transfer-free, comfortable to use, and safe. It provides high quality makeup cosmetics.
従来あるメイクアップ化粧料においては経時的に、皮脂
や汗の分泌により落らてしまったり、まぶたなどのよう
に常に運動している部分ではその物理的影響で落ちてし
まったり、物に触れたとき色が移ったり(以下転色と称
す)して化粧直しの手間、衣服、物が汚れるなどの欠点
を有していた。Conventional make-up cosmetics tend to fall off over time due to sebum and sweat secretion, or may fall off due to physical effects on areas that are constantly exercised, such as the eyelids, or may fall off due to contact with objects. This has disadvantages, such as color transfer (hereinafter referred to as color transfer), which requires a lot of effort to redo makeup, and stains clothes and objects.
そこで、上記欠点を解決するために、化粧料組成に揮発
性油剤を加え、塗布後、揮発性油剤の揮発により、強固
な塗布膜を形成することができるメイクアップ化粧料が
開発され、何種か商品化されている。Therefore, in order to solve the above-mentioned drawbacks, makeup cosmetics have been developed that can add volatile oils to the cosmetic composition and form a strong coating film by volatilization of the volatile oils after application. or has been commercialized.
しかしながら、これらは落ちにくさという点では十分に
機能を有してはいるが、揮発油を配合しているために安
全性に劣るという欠点を生じている。 また、これらの
揮発性油剤は揮発性が高いため、容器の気密性に細心の
注意を払う必要があったり、塗布時ののびが悪くなるな
どの使用上の問題も生じている。However, although these have sufficient functionality in terms of being difficult to remove, they have the disadvantage of being inferior in safety because they contain volatile oil. Furthermore, since these volatile oils have high volatility, there are problems in use, such as the need to pay close attention to the airtightness of the container and poor spreadability during application.
逆に、低揮発性の油剤を使用すると、他の原料との相溶
性が悪くなり製品の安定性が低下したり、塗布後の乾燥
時間が区くなり転色しやすくなる。On the other hand, if a low-volatility oil is used, the compatibility with other raw materials will be poor, resulting in a decrease in product stability, and the drying time after application will be longer, making discoloration more likely.
そこで本発明者は、係る事情に鑑みて鋭意研究を行なっ
た結果、揮発性油剤としてジメチルポリシロキサン(粘
度1.5cs)と環状ポリジメチルシロキサン(5量体
および/または6量体)とを併用することにより、各々
単独で用いた場合に比べて上記の欠点が大きく改善され
ることを見い出し、本発明を完成させるに至った。Therefore, as a result of intensive research in view of the above circumstances, the present inventors have found that dimethylpolysiloxane (viscosity 1.5 cs) and cyclic polydimethylsiloxane (pentamer and/or hexamer) are used in combination as volatile oil agents. It has been found that by doing so, the above-mentioned drawbacks can be greatly improved compared to when each is used alone, and the present invention has been completed.
本発明品の安全性を確認するためにこれらの揮発性油剤
と、一般に化粧料によく使用されている揮発性油剤につ
いて家兎皮膚−次刺激性試験を行った。 試験はDra
ize法に準じた。 結果を表1に示す。In order to confirm the safety of the products of the present invention, a rabbit skin irritation test was conducted on these volatile oils and other volatile oils commonly used in cosmetics. The exam is Dra
According to the ize method. The results are shown in Table 1.
表1.家兎皮膚−次刺激性試験
(表中の値は刺激値を示す)
*本発明に用いた揮発性油剤
本発明を構成する他の成分は、被膜形成剤、粉体基剤お
よび可塑剤であり、本発明に用いられる被膜形成剤は、
セレシン、オシケライト、マイクロクリスタリンワック
ス、固形パラフィン、ミツロウ、カルナウバロウ、キャ
ンデリラロウ、硬化油、エポキシ樹脂の高級脂肪酸エス
テル、ポリエチレン、ジメチルトリメチルポリシロキサ
ン、モノメチルポリシロキサン、アビエチン酸グリセリ
ンエステルの一種又は二種以上の組合せがのぞましい。Table 1. Rabbit skin secondary irritation test (values in the table indicate irritation values) *Volatile oil used in the present invention Other components constituting the present invention include a film forming agent, a powder base, and a plasticizer. The film forming agent used in the present invention is
One or more of ceresin, osikelite, microcrystalline wax, solid paraffin, beeswax, carnauba wax, candelilla wax, hydrogenated oil, higher fatty acid ester of epoxy resin, polyethylene, dimethyltrimethylpolysiloxane, monomethylpolysiloxane, abietic acid glycerin ester A desirable combination.
本発明に用いられる粉体基剤には1通常化粧料に用いら
れるもので、例えばタルク、マイカ、カオリン、セリサ
イト、酸化チタン、酸化鉄、有機顔料、グンジョウ、コ
ンジヨウなどが挙げられる。Powder bases used in the present invention include those commonly used in cosmetics, such as talc, mica, kaolin, sericite, titanium oxide, iron oxide, organic pigments, turmeric, and chinensis.
本発明に用いられる可塑剤には、通常化粧料に用いられ
る液状またはペースト状油分で、例えばスクワラン、ヒ
マシ油、流動パラフィン、2−エチルヘキサン酸セチル
、トリー2−エチルヘキサン酸グリセリン、ミリスチン
酸オクチルドデシル。Plasticizers used in the present invention include liquid or paste oils commonly used in cosmetics, such as squalane, castor oil, liquid paraffin, cetyl 2-ethylhexanoate, glycerin tri-2-ethylhexanoate, and octyl myristate. Dodecyl.
オクチルドデカノール、ワセリン、ラノリン、ジペンタ
エリトリット脂肪酸エステル、ラノリン誘導体、流動ポ
リイソブチレンなどが挙げられる。Examples include octyldodecanol, vaseline, lanolin, dipentaerythritol fatty acid ester, lanolin derivatives, and fluid polyisobutylene.
さらに、本発明のメイクアップ化粧料には、上記成分の
ほか、水、乳化剤、顔料、染料、顔料分散剤、香料、防
腐剤、パール剤、樹Jlif等を適宜添加することがで
きる。 本発明の落ちにりく、転色せず、使用感が良く
、かつ安全性の高いメイクアップ化粧料を装造するには
、油性系の場合、粉体基剤(1〜50重量部)に対し、
揮発性油剤(10〜60重量部)、被膜形成剤(0,5
〜40重量部)可塑剤(0,5〜40重量部)を加えて
混練するものであり、乳化系の場合は、さらに乳化剤。Furthermore, in addition to the above-mentioned components, water, emulsifiers, pigments, dyes, pigment dispersants, perfumes, preservatives, pearlescent agents, and Jlif can be appropriately added to the makeup cosmetics of the present invention. In order to formulate the makeup cosmetics of the present invention that are non-sticky, non-color changing, comfortable to use, and highly safe, in the case of oil-based cosmetics, powder base (1 to 50 parts by weight) must be added. On the other hand,
Volatile oil (10 to 60 parts by weight), film forming agent (0.5 parts by weight)
~40 parts by weight) A plasticizer (0.5 to 40 parts by weight) is added and kneaded, and in the case of an emulsifying system, an emulsifier is also added.
精製水、保湿剤等を本混練物を油相として乳化させるも
ので、性状によってはチューブ充填、流し込み充填など
の商品形態となるものである。Purified water, a humectant, etc. are emulsified using this kneaded product as an oil phase, and depending on the properties, the product can be filled in a tube, poured, etc.
本発明の最大目的とする転色しないという条件を満足さ
せるには、被膜形成剤と可塑剤と粉体基剤との配合比が
重要であり、肌へ塗布したのち、揮発性油剤が揮発後こ
れらが被膜となるわけで、これら比率は、粉体基剤1に
対し、被膜形成剤が0、1〜1.0.可塑剤が0.1〜
0.9の割合で配合するのが最も好ましい。In order to satisfy the condition of no discoloration, which is the main objective of the present invention, the blending ratio of the film forming agent, plasticizer, and powder base is important. These form a film, and the ratio is 1 to 1 part of the powder base to 0,1 to 1.0 of the film forming agent. Plasticizer is 0.1~
Most preferably, the ratio is 0.9.
可塑剤の比率が高くなると、被膜の強さが弱くなって物
理的な影響でたやすく転色しやすくなり、また小さくな
ると、肌に違和感を感じてきたり、のびがわるくなった
りなどの傾向があられれる。When the ratio of plasticizer increases, the strength of the film becomes weaker, making it easier to discolor due to physical effects, and when the ratio of plasticizer becomes smaller, it tends to feel uncomfortable on the skin and become difficult to spread. Hail!
被膜形成剤の比率では、その逆の傾向を示す。The ratio of film-forming agents shows the opposite trend.
よってこれらの配合比には十分注意を払う必要がある。Therefore, it is necessary to pay sufficient attention to these compounding ratios.
本発明について実施例をあげてさらに説明する。 The present invention will be further explained by giving examples.
これらは本発明を何ら限定するものではない。These do not limit the present invention in any way.
安全性試験17L
(])試験方法
21〜43才の健康な女性20名を被験者とし、実施1
9111および、従来品の比較例1を試料として48時
間閉塞バッチテストを行なった。Safety test 17L (])Test method 20 healthy women aged 21 to 43 were used as subjects, and test 1 was conducted.
A 48-hour closed batch test was conducted using 9111 and Comparative Example 1, a conventional product, as samples.
被 験 者:健常人女子20名、年齢21〜43才貼布
部位 :後背部
テストプラスター: Al−test plaster
塗布量: 0.04艷
(2)判定方法
48時間閉塞貼布後剥離し、剥Fa2時間後、24時間
後に以下の基準に従い判定を行った。Subjects: 20 healthy females, ages 21-43 Application site: Back Test plaster: Al-test plaster
Coating amount: 0.04 (2) Judgment method After applying the patch for 48 hours, it was peeled off, and after 2 hours and 24 hours of peeling off, the patch was judged according to the following criteria.
−m−−・−無反応
± −−疑陽性
→−−−−−−紅斑
利 −−−−−一 紅斑および丘疹
(以下余白)
(3)処方および製造方法
表2 ファンデーション実施例1と比較例1処方製造方
法
(1)〜(7)を75〜80℃にて加熱溶解する。これ
に別途混合粉砕均一化した(8)〜α■を加え混練した
後、三本ローラーにて分散処理し、実施例1.比較例1
のファンデーションを得た。-m--・-No reaction± ---False positive→---------Erythema and papules (hereinafter referred to as margins) (3) Prescription and manufacturing method Table 2 Comparison with Foundation Example 1 Example 1 Prescription manufacturing method (1) to (7) are heated and dissolved at 75 to 80°C. After adding and kneading (8) to α■, which were separately mixed and homogenized, the mixture was dispersed using three rollers. Comparative example 1
I got the foundation.
(4)結果
表3.バッチテスト結果
以上の結果から明らかなように本発明品である実施例1
のファンデーションの安全性が確認された。(4) Results table 3. Batch test results As is clear from the above results, Example 1 is a product of the present invention.
The safety of the foundation was confirmed.
転色試験方法
(1)試験方法
実施例2および比較例2について下記の試験を行なった
。Color change test method (1) Test method The following tests were conducted for Example 2 and Comparative Example 2.
■試料に紫外線吸収剤エスカロール507 (2−E
thylllexyl p−Dimethylamin
obenzoate )を4%添加し、この試料の一定
量(20mg )を人前腕内側の一定面積(16c+(
)に塗布する。 次ぎに皮膚接触部に試験紙を装着した
器具で、塗布部を’l kg / ctで抑圧を3回繰
り返した。■Ultraviolet absorber Escarol 507 (2-E)
thyllexyl p-dimethylamine
4% obenzoate) was added, and a certain amount (20 mg) of this sample was applied to a certain area (16c+(
). Next, the application area was repeatedly compressed three times at 1 kg/ct using a device with a test strip attached to the skin contact area.
試験紙から紫外線吸収剤をエタノールで抽出し、ロ立ダ
ブルビーム分光光度計228型を使用し3】Onmの吸
光度を測定した。The ultraviolet absorber was extracted from the test paper with ethanol, and the absorbance at 3] Onm was measured using a double beam spectrophotometer model 228.
転角度は以下の式により算出した。The rotation angle was calculated using the following formula.
■女性30名からなるパネルにより、べたつき感、のび
、化粧持ち、密着感9食器への転色、ティ・ノシュでの
とれの5項目につき、5段階評価で行なった。 なお、
点数が高いほど良好なことを示す。■A panel of 30 women evaluated the products on a 5-point scale based on 5 items: stickiness, spreadability, makeup retention, adhesion, discoloration on tableware, and removal on Ti Noche. In addition,
The higher the score, the better.
ここで、食器への転色のテスト方法は、口紅塗布5分後
、5秒間口に白色のコーヒー力・ノブをくわえ、肉眼に
て口紅のコーヒーカップへの移りぐあいを判断する。Here, to test the color transfer to tableware, 5 minutes after applying the lipstick, hold a white coffee knob in your mouth for 5 seconds and visually judge the transfer of the lipstick to the coffee cup.
ティッシュでのとれのテスト方法は、口紅塗布5分後、
ティ、シュの移りぐあいを判断する。The test method for removing lipstick with a tissue is to apply it 5 minutes after applying the lipstick.
Judge the transition between tee and sh.
(以下余白)
(2)処方および製造方法
表4 口紅実施例2と比較例2処方
製造方法
(1)〜(9)を95℃にて加熱溶解する。 これに別
途混合粉砕均一化したαO)〜(2)を加え混練した後
、三本ローラーにて分散処理し、実施例2.比較例2の
口紅を得た。(The following is a blank space) (2) Prescription and manufacturing method Table 4 Lipstick Example 2 and Comparative Example 2 Prescription Manufacturing Methods (1) to (9) are heated and dissolved at 95°C. After adding and kneading αO) to (2), which were separately mixed and homogenized, the mixture was dispersed using three rollers. A lipstick of Comparative Example 2 was obtained.
(3)結果
表5.第1法による結果
表6.第2法による結果
以上の結果から明らかなように本発明品である実施例2
の口紅は、その優れた使用感および転色しにくさが確認
された。(3) Results table 5. Results table according to method 1 6. Results from Method 2 As is clear from the above results, Example 2 is a product of the present invention.
The lipstick was confirmed to have excellent usability and resistance to discoloration.
実施例3. アイシャドウ
(処方) 重量%(1)環
状ポリジメチルシロキサンS ffi体10.0(2)
環状ポリジメチルシロキサン6ffi体 20.0(
3)ジメチルポリシロキサン(1,5C5) 1
0.0(4)カルナウバロウ
10.0(5)エポキシ樹脂の高級脂肪酸エステル
1.0(6)ステアリン酸アルミニウム
2.0(7)吸着精製ラノリン
0゜5(8)流動パラフィン
0.3(9)バラオキシ安息香酸メチル
0.100)タルク
20.10υ雲母チタン
l0000の酸化チタン
5.003)群青
10.0(2)黒酸化鉄
1.0(製法)
(11〜(8)を85°Cにて加熱溶解する。これに別
途混合粉砕均一化した(9)〜04]を加え混練した後
、三本ローラーにて分散処理をし、容器、若しくは成形
型に流し込みアイシャドウを得る。Example 3. Eyeshadow (formulation) Weight % (1) Cyclic polydimethylsiloxane S ffi form 10.0 (2)
Cyclic polydimethylsiloxane 6ffi 20.0 (
3) Dimethylpolysiloxane (1,5C5) 1
0.0(4) Carnauba wax
10.0(5) Higher fatty acid ester of epoxy resin
1.0(6) Aluminum stearate
2.0 (7) Adsorption purified lanolin
0゜5(8) Liquid paraffin
0.3(9) Methyl roseoxybenzoate
0.100) Talc
20.10υ mica titanium
10000 titanium oxide
5.003) Ultramarine
10.0(2) Black iron oxide
1.0 (Production method) (11 to (8) are heated and dissolved at 85°C. Separately mixed and homogenized (9) to 04) are added and kneaded, and then dispersion treatment is performed using three rollers. Then, pour it into a container or mold to obtain an eye shadow.
以上の如くして得られたアイシャドウは、優れた使用感
をもち、落ちに<<、かつ安全性の高いアイシャドウで
あった。また、安定性も長期間良好であった。The eye shadow obtained as described above had an excellent feeling of use, was easy to remove, and was highly safe. Moreover, stability was also good for a long period of time.
実施例4. 頬紅
(処方) 重量%(11環
状ポリジメチルシロキサン6量体 20.0(2)ジ
メチルポリシロキサン(1,5CS) 20.0(
3)固形パラフィン 5.0(
4)ミツロウ 2.0(
5)セレシン 5.0(
6)スクワラン 5.0(
7)ブチルヒドロキシアニソール 0.1(
8)赤色226号 1.5
(9)酸化チタン 2・5
00)マイカ 38.
9(製法)
(1)〜(7)を80〜85°Cにて加熱溶解する。こ
れに別途混合粉砕均一化した(8)〜aO)を加え混練
した後、三本ローラーにて分散処理をし、容器、若しく
は成形型に流し込み頬紅を得る。Example 4. Blush (prescription) Weight % (11-cyclic polydimethylsiloxane hexamer 20.0(2) dimethylpolysiloxane (1,5CS) 20.0(
3) Solid paraffin 5.0 (
4) Beeswax 2.0 (
5) Ceresin 5.0 (
6) Squalane 5.0 (
7) Butylhydroxyanisole 0.1 (
8) Red No. 226 1.5
(9) Titanium oxide 2.5
00) Mica 38.
9 (Production method) (1) to (7) are heated and dissolved at 80 to 85°C. After adding and kneading (8) to aO), which were separately mixed and homogenized, the mixture is dispersed using three rollers and poured into a container or a mold to obtain a blusher.
以上の如くして得られた頬紅は、優れた使用感をもち、
落ちにくく、かつ安全性の高い頬紅であった。また安定
性も長期間良好であった。The blusher obtained as described above has an excellent feeling of use,
It was a blush that did not easily come off and was highly safe. The stability was also good over a long period of time.
実施例5. 0/W乳化型フアンデーシヨン(処方)
(重量部)(1)環状ポリ
ジメチルシロキサン5量体 4.50(2)環状ポ
リジメチルシロキサン6量体 2.00(3)ジメ
チルポリシロキサン(1,5C3) 4.00(
4)カルナウバロウ 2.5
0(5)キャンデリラロウ 1.
20(6)オシケライト 1
.30(7)ラノリン
2.00(8)流動パラフィン
2.50(9)ポリオキシエチレンソルビタン
モノオレイン酸エステル(Tween 80) 1.
0000)ソルビタンモノオレイン酸エステル(Spa
n 80 ) 1.00
0υモノステアリン酸グリセリン(親油型) 0.7
002)エポキシ樹脂の高級脂肪酸エステル 0.2
003)ベンガラ
0.11(2)黄酸化鉄
0.23αつ黒酸化鉄
0.06叫酸化チタン 1
.4007)タルク
6.8008)カオリン
9.200(ト)精製水
55.60(イ)プロピレングリコール
3.5(21)防腐剤
0.10(社)香料
0.10(製法)
(1)〜02)の浦和を80〜85°Cにて加熱溶解す
る。これに別途0湯〜08)を混合粉砕均一化し、0■
〜(21)を加え、均一に分散させたものを徐々に加え
、ホモミキサーで乳化後冷却する。 50°Cにて(社
)を加え室温まで冷却後、容器に充填しファンデーショ
ンを得る。Example 5. 0/W emulsifying foundation (prescription)
(Parts by weight) (1) Cyclic polydimethylsiloxane pentamer 4.50 (2) Cyclic polydimethylsiloxane hexamer 2.00 (3) Dimethylpolysiloxane (1,5C3) 4.00 (
4) Carnauba wax 2.5
0(5) Candelilla Row 1.
20(6) Osikelite 1
.. 30(7) Lanolin
2.00 (8) Liquid paraffin
2.50(9) Polyoxyethylene sorbitan monooleate (Tween 80) 1.
0000) Sorbitan monooleate (Spa
n 80 ) 1.00 0υ Glyceryl monostearate (lipophilic type) 0.7
002) Higher fatty acid ester of epoxy resin 0.2
003) Bengala
0.11(2) Yellow iron oxide
0.23α black iron oxide
0.06 titanium oxide 1
.. 4007) Talc
6.8008) Kaolin
9.200 (g) Purified water
55.60 (a) Propylene glycol
3.5 (21) Preservatives
0.10 (company) fragrance
0.10 (Production method) Urawa (1) to 02) is heated and dissolved at 80 to 85°C. Separately, mix 0~08) to this to homogenize the 0■
- (21) are added and uniformly dispersed, then gradually added, emulsified with a homomixer, and then cooled. Co., Ltd. at 50°C, cooled to room temperature, and then filled into a container to obtain a foundation.
以上の如くして得られたファンデーションは、優れた使
用感をもち、落ちにくく、かつ安全性の高いファンデー
ションであった。また安定性も長期間良好であった。The foundation obtained as described above had an excellent feeling of use, was hard to fall off, and was highly safe. The stability was also good over a long period of time.
実施例6. アイライナー
(処方) 重量%(1)環
状ポリジメチルシロキサン6量体 2.00(2)
ジメチルポリシロキサン(1,5C3’) 3.
00(3)キャンデリラロウ 6
.00(4)オシケライト
3.50(5)アビエチン酸グリセリンエステル
0.30(6)モノステアリン酸グリセリン
(自己乳化型) 1.00(7
)モノステアリン酸ソルビタン 0.20(
8)ステアリン酸 1.0
0(9)I青 製氷
52.0500)ヒドロキシエチルセルロース
0.050υコロイド性含水ケイ酸アルミニウムマ
グネシウム 0.500力水酸
化カリウム 0.2003)ア
クリル酸エチルメタクリル酸
メチル共重合体 10.0004〕
黒酸化鉄 15.000ω
タルク 5.0
006)防腐剤・香料 0.
20(製法)
(1)〜(8)を80〜85℃にて加熱溶解する。これ
に別途(9)に00)〜Q51を混合粉砕均一化し、前
者に加えホモミキサーで乳化後、冷却する。Example 6. Eyeliner (formulation) Weight% (1) Cyclic polydimethylsiloxane hexamer 2.00 (2)
Dimethylpolysiloxane (1,5C3') 3.
00(3) Candelilla Row 6
.. 00(4) Osikelite
3.50(5) Abietic acid glycerin ester
0.30 (6) Glyceryl monostearate (self-emulsifying type) 1.00 (7
) Sorbitan monostearate 0.20 (
8) Stearic acid 1.0
0(9)I blue ice making
52.0500) Hydroxyethylcellulose
0.050υ colloidal hydrous aluminum magnesium silicate 0.500p potassium hydroxide 0.2003) Ethyl acrylate methyl methacrylate copolymer 10.0004]
Black iron oxide 15.000Ω
Talc 5.0
006) Preservatives/Fragrances 0.
20 (Production method) (1) to (8) are heated and dissolved at 80 to 85°C. Separately, in step (9), 00) to Q51 are mixed, ground, and homogenized, added to the former, emulsified in a homomixer, and then cooled.
50℃にて(6)を加え室温まで冷却後、容器に充填し
製品とする。Add (6) at 50°C, cool to room temperature, and then fill in a container to prepare a product.
以上の如くして得られたアイライナーは、優れた使用感
をもち、落ちに<<、転色もせず、かつ安全性の高いア
イライナーであった。また安定性も長期間良好であった
。The eyeliner obtained as described above had an excellent feeling of use, did not fall off easily, did not discolor, and was highly safe. The stability was also good over a long period of time.
実施例7. 0/W乳化型フアンデーシヨン(処方)
(重量部)(1)環状ポリ
ジメチルシロキサン5常体 2.00(2)環状ポ
リジメチルシロキサン6量体 2゜03(3)ジメ
チルポリシロキサン(1,5C5)11.01(4)ス
クワラン 5.43(5)オ
シケライト 2.28(6)
モノメチルポリシロキサン 5.05(7
)ラノリン 3.8
1(8)マグネシウムステアレエート 0.
29(9)ジグリセリルジオレエート 3
.7600)ベンガラ
0・4201〕黄酸化鉄
0.1102)刀Aへり化1失
0.0803)タルク
6.32Q4〕漆青 ルM 水
49.2105)グリセリン
8.00011O香料・防腐
剤 0.20(製法)
(1)〜(9)を80〜85°Cにて混合溶解し、均一
化後、(101〜0■を加え均一に分散する。Example 7. 0/W emulsifying foundation (prescription)
(Parts by weight) (1) Cyclic polydimethylsiloxane pentamer 2.00 (2) Cyclic polydimethylsiloxane hexamer 2°03 (3) Dimethylpolysiloxane (1,5C5) 11.01 (4) Squalane 5. 43(5) Osichelite 2.28(6)
Monomethylpolysiloxane 5.05 (7
) Lanolin 3.8
1(8) Magnesium stearate 0.
29(9) diglyceryl dioleate 3
.. 7600) Bengala
0.4201] Yellow iron oxide
0.1102) Katana A edge conversion 1 loss
0.0803) Talc
6.32Q4] Lacquer blue Le M water
49.2105) Glycerin
8.00011O fragrance/preservative 0.20 (manufacturing method) (1) to (9) are mixed and dissolved at 80 to 85°C, and after homogenization, (101 to 0) is added and dispersed uniformly.
これに別途80℃にて混合溶解させた(2)〜αG)を
添加し、ホモミキサーを用い乳化し、冷却後製品とする
。(2) to αG), which were separately mixed and dissolved at 80°C, are added to this, emulsified using a homomixer, and after cooling, a product is obtained.
以上の如くして得られたファンデーションは、優れた使
用感をもち、落ちにくく、転色もせず、かつ安全性の高
いファンデーションであった。また安定性も長期間良好
であった。The foundation obtained as described above had an excellent feeling of use, was hard to remove, did not discolor, and was highly safe. The stability was also good over a long period of time.
Claims (3)
須成分として含有することを特徴とするメイクアップ化
粧料。(1) A makeup cosmetic characterized by containing a volatile oil, a film-forming agent, a powder base, and a plasticizer as essential ingredients.
粘度が1.5センチストークス)および環状ポリジメチ
ルシロキサンからなる特許請求範囲第1項記載のメイク
アップ化粧料。(2) The volatile oil agent is low molecular weight dimethylpolysiloxane (
1.5 centistokes) and a cyclic polydimethylsiloxane.
たは6量体である特許請求範囲第1項記載のメイクアッ
プ化粧料。(3) The makeup cosmetic according to claim 1, wherein the cyclic polydimethylsiloxane is a pentamer and/or a hexamer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60203064A JPS6261911A (en) | 1985-09-12 | 1985-09-12 | Makeup cosmetic |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60203064A JPS6261911A (en) | 1985-09-12 | 1985-09-12 | Makeup cosmetic |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6261911A true JPS6261911A (en) | 1987-03-18 |
Family
ID=16467738
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60203064A Pending JPS6261911A (en) | 1985-09-12 | 1985-09-12 | Makeup cosmetic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6261911A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63159489A (en) * | 1986-12-23 | 1988-07-02 | Shin Etsu Chem Co Ltd | Gel composition |
JPS63275518A (en) * | 1987-05-08 | 1988-11-14 | Terumo Corp | Semisolid composition |
JPH06199630A (en) * | 1992-12-15 | 1994-07-19 | Revlon Consumer Prod Corp | Improved anti-transferring cosmetics composition |
JPH07267826A (en) * | 1994-03-29 | 1995-10-17 | Shiseido Co Ltd | Composition for rouge |
US5837223A (en) * | 1996-08-12 | 1998-11-17 | Revlon Consumer Products Corporation | Transfer resistant high lustre cosmetic stick compositions |
JPH11502873A (en) * | 1996-01-16 | 1999-03-09 | ザ、プロクター、エンド、ギャンブル、カンパニー | Color transfer resistant lip composition |
FR2819398A1 (en) * | 2001-01-17 | 2002-07-19 | Oreal | Composition useful in cosmetics, especially foundation sticks, comprises lipophilic liquid and low molecular weight polymer |
WO2002065994A1 (en) * | 2001-02-19 | 2002-08-29 | Kanebo, Limited | Cosmetics and process for producing cosmetics |
US6565862B1 (en) | 1999-01-28 | 2003-05-20 | L'oreal S.A. | Makeup or care composition comprising a hydrophilic organopolysiloxane |
JP2006273829A (en) * | 2005-03-25 | 2006-10-12 | Ookemu Tsusho Kk | Powder for cosmetic and the resultant cosmetic |
JP2008291704A (en) * | 2007-05-23 | 2008-12-04 | Honda Motor Co Ltd | Cooling structure for piston of internal combustion engine |
US11033340B2 (en) | 2015-10-01 | 2021-06-15 | Sony Corporation | Medical support arm apparatus and medical system |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5576612A (en) * | 1978-12-01 | 1980-06-09 | Kenji Nakamura | Cosmetic applying tool and its preparation |
JPS56114711U (en) * | 1980-02-05 | 1981-09-03 | ||
JPS56120336A (en) * | 1980-02-08 | 1981-09-21 | Takiron Co | Puff for dressing and its manufacture |
-
1985
- 1985-09-12 JP JP60203064A patent/JPS6261911A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5576612A (en) * | 1978-12-01 | 1980-06-09 | Kenji Nakamura | Cosmetic applying tool and its preparation |
JPS56114711U (en) * | 1980-02-05 | 1981-09-03 | ||
JPS56120336A (en) * | 1980-02-08 | 1981-09-21 | Takiron Co | Puff for dressing and its manufacture |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0471114B2 (en) * | 1986-12-23 | 1992-11-12 | Shinetsu Chem Ind Co | |
JPS63159489A (en) * | 1986-12-23 | 1988-07-02 | Shin Etsu Chem Co Ltd | Gel composition |
JPS63275518A (en) * | 1987-05-08 | 1988-11-14 | Terumo Corp | Semisolid composition |
JPH0572886B2 (en) * | 1987-05-08 | 1993-10-13 | Terumo Corp | |
JPH06199630A (en) * | 1992-12-15 | 1994-07-19 | Revlon Consumer Prod Corp | Improved anti-transferring cosmetics composition |
JPH07267826A (en) * | 1994-03-29 | 1995-10-17 | Shiseido Co Ltd | Composition for rouge |
JPH11502873A (en) * | 1996-01-16 | 1999-03-09 | ザ、プロクター、エンド、ギャンブル、カンパニー | Color transfer resistant lip composition |
US5837223A (en) * | 1996-08-12 | 1998-11-17 | Revlon Consumer Products Corporation | Transfer resistant high lustre cosmetic stick compositions |
US6565862B1 (en) | 1999-01-28 | 2003-05-20 | L'oreal S.A. | Makeup or care composition comprising a hydrophilic organopolysiloxane |
USRE39495E1 (en) * | 1999-01-28 | 2007-02-27 | L'oreal S.A. | Makeup or care composition comprising an at least partially crosslinked elastomeric solid organopolysiloxane |
FR2819398A1 (en) * | 2001-01-17 | 2002-07-19 | Oreal | Composition useful in cosmetics, especially foundation sticks, comprises lipophilic liquid and low molecular weight polymer |
WO2002056845A1 (en) * | 2001-01-17 | 2002-07-25 | L'oreal | Composition structured in rigid form by a polymeric compound |
WO2002065994A1 (en) * | 2001-02-19 | 2002-08-29 | Kanebo, Limited | Cosmetics and process for producing cosmetics |
JP2006273829A (en) * | 2005-03-25 | 2006-10-12 | Ookemu Tsusho Kk | Powder for cosmetic and the resultant cosmetic |
JP4721041B2 (en) * | 2005-03-25 | 2011-07-13 | オーケム通商株式会社 | Cosmetic powder and cosmetics |
JP2008291704A (en) * | 2007-05-23 | 2008-12-04 | Honda Motor Co Ltd | Cooling structure for piston of internal combustion engine |
US11033340B2 (en) | 2015-10-01 | 2021-06-15 | Sony Corporation | Medical support arm apparatus and medical system |
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