JPS6143326B2 - - Google Patents

Info

Publication number
JPS6143326B2
JPS6143326B2 JP9395678A JP9395678A JPS6143326B2 JP S6143326 B2 JPS6143326 B2 JP S6143326B2 JP 9395678 A JP9395678 A JP 9395678A JP 9395678 A JP9395678 A JP 9395678A JP S6143326 B2 JPS6143326 B2 JP S6143326B2
Authority
JP
Japan
Prior art keywords
makeup
oil
cosmetic
formulation
present
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.)
Expired
Application number
JP9395678A
Other languages
Japanese (ja)
Other versions
JPS5520735A (en
Inventor
Yutaka Okunuki
Shigenori Kumagai
Michiko Nara
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shiseido Co Ltd
Original Assignee
Shiseido Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Shiseido Co Ltd filed Critical Shiseido Co Ltd
Priority to JP9395678A priority Critical patent/JPS5520735A/en
Publication of JPS5520735A publication Critical patent/JPS5520735A/en
Publication of JPS6143326B2 publication Critical patent/JPS6143326B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/58Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • A61K8/585Organosilicon compounds

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、化粧料に、シリコン―カーボン結合
を有する有機シリコン化合物を配合した化粧料特
にメーキヤツプ化粧料に関する。 一般の油性メーキヤツプ化粧料は、スチツク
状、クリーム状を問わず皮膚に塗布する際、滑ら
かにのび、仕上りはきれいであるが、油つぽい、
ベタつく、経時で化粧くずれがはげしい等欠点も
多い。 本発明者等は、油性メーキヤツプ化粧料の特徴
を有し、欠点を回避する目的で、揮発性油分に着
目し、探索してきた。 揮発性油分を配合した化粧料は、油性メーキヤ
ツプ化粧料の特徴である塗布時の滑らかさ、の
び、ぼかし易さ等を有し、さらに塗布後は、油特
有のベタつきがなく、さつぱりしており、経時で
の化粧くずれがない等、利点が多い。 ところで化粧品原料として具備しなくてはなら
ない無味・無臭・無害という条件を満足する揮発
性物質は、非常に限定され、わずかに低沸点炭化
水素、低重合度の環状・鎖状ジメチルポリシロキ
サンが公知のものとして使われている。 しかし低沸点炭化水素は、原料特有の匂いがあ
り又、環状・鎖状ジメチルポリシロキサンは、他
成分との相溶性の点で処方構成上の制約がある。 本発明者等は、シリコン・カーボン結合を有す
る有機シリコン化合物を配合する事により、前述
した様な欠点をカバーした優れた特性を有する化
粧料を得た。 すなわち、本発明は、下記一般式()で示さ
れる有機シリコン化合物の一種又は二種以上を配
合したことを特徴とする化粧料である。 (ただし、式中Rは各々独立にメチルキ基又は
エチル基を示し、nは0または1の整数を示
す。)ここで用いた有機シリコン化合物の沸点は
表に示す通りである。 又前述の一般式()中のRがさらに炭素数の
大きなプロピル基、ブチル基……も考えられる
が、この場合は、沸点が蓄しく高まり本発明の主
旨からはずれる。
The present invention relates to cosmetics, particularly makeup cosmetics, containing organic silicon compounds having silicon-carbon bonds. General oil-based makeup cosmetics, whether in stick or cream form, spread smoothly and have a beautiful finish when applied to the skin, but they tend to be oily or oily.
It has many drawbacks, such as being sticky and causing makeup to fade over time. The present inventors have focused on and have been searching for volatile oil components that have the characteristics of oil-based makeup cosmetics and avoid the drawbacks. Cosmetics containing volatile oils have the characteristics of oil-based makeup cosmetics, such as smoothness, spreadability, and ease of blurring when applied, and also have a refreshing feel without the stickiness characteristic of oils. It has many advantages, such as the fact that the makeup does not fade over time. By the way, volatile substances that satisfy the requirements of being tasteless, odorless, and harmless as cosmetic ingredients are extremely limited, and only low-boiling-point hydrocarbons and cyclic/chain dimethylpolysiloxanes with a low degree of polymerization are known. It is used as a thing. However, low-boiling hydrocarbons have a characteristic odor as a raw material, and cyclic/chain dimethylpolysiloxanes have restrictions on formulation composition in terms of compatibility with other components. The present inventors have obtained a cosmetic having excellent properties that overcome the above-mentioned drawbacks by blending an organic silicon compound having a silicon-carbon bond. That is, the present invention is a cosmetic material containing one or more organic silicon compounds represented by the following general formula (). (However, in the formula, R each independently represents a methyl group or an ethyl group, and n represents an integer of 0 or 1.) The boiling points of the organosilicon compounds used here are as shown in the table. It is also conceivable that R in the above-mentioned general formula () may have a larger number of carbon atoms, such as a propyl group or a butyl group, but in this case, the boiling point would increase significantly and depart from the gist of the present invention.

【表】 また、本発明に用いられるシリコン化合物と他
のシリコン化合物の、各種化粧品原料への溶解性
の比較を表に示す。 表中、A、B、Cは各々ヘキサメチルシロキサ
ン、シクロペンタジメチルシロキサン、ヘキサメ
チルジシリールメチレンを示す。
[Table] The table also shows a comparison of the solubility of the silicon compound used in the present invention and other silicon compounds in various cosmetic raw materials. In the table, A, B, and C represent hexamethylsiloxane, cyclopentadimethylsiloxane, and hexamethyldisilylmethylene, respectively.

〔合成例 1〕[Synthesis example 1]

エチルエーテル200gにヘキサクロルジシリル
メチレン238gを加え更にメチルマグネシウムブ
ロマイド6モルを加えて塩酸酸性下で80℃、3時
間反応させ、145gのヘキサメチルジシリルメチ
レンを得る。 〔合成例 2〕 ペンタン500ml中にトリメチルシリルメチルリ
チウム0.5モルとジメチルジクロルシラン0.155モ
ルを加え12時間還流させ、その後90℃、12時間加
熱を続けて、86%の収率でオクタメチルトリシリ
ルメチレンを得る。 次に本発明の実施例を示す。 〔実施例1〕フアウンデイシヨン (処方) ヘキサエチルジシリルメチレン 40(重量部) カルナウバワツクス 1 マイクロクリスタリンワツクス 6 有機変性モンモリロナイト 2(重量部) ソルビタンモノオレート 1 マイカ 20 タルク 10 酸化チタン 15 酸化鉄 5 香料 適量 得られたフアウンデイシヨンは、塗布する際、
滑らかにのび、数分間でヘキサエチルジシリルメ
チレンが揮散する。その後は、さつぱりした感じ
で肌に密着して化粧くずれしにくく、海水浴等で
も全く落ちない耐水性を兼備している。 〔実施例2〕マスカラ (処方) ヘキサメチルジシリルメチレン 52(重量部) カルナウバワツクス 5 キヤンデリラワツクス 3 マイクロクリスタリンワツクス 9 コレステロール 1 ソルビタンモノステアレート 1 ジアルキルジタローアンモニウムセルロース誘
導体 3 アルミニウムステアレート 1 精製水 5 タルク 8 酸化鉄黒 12 香料 適量 まばたき等により、下瞼に着色するという従来
の油性マスカラの欠点が全くなく、経時の化粧も
ちが良く、耐水性も優れたマスカラが得られた。 〔実施例3〕アイライナー (処方) ヘキサメチルジシリルメチレン 50(重量部) ビーワツクス 5 カルナウバワツクス 3 テルペン系樹脂 10 有機変性ベントナイト 2 セルロース誘導体 5 酸化鉄黒 10 タルク 5 精製水 10 香料 適量 実施例2のマスカラと同様、ヘキサメチルジシ
リルメチレン揮散後は、耐水性、耐油性に優れた
アイライナーが得られた。 〔実施例4〕アイシヤドウ 処方) オクタメチルトリシリルメチレン 40(重量部) 有機変性ベントナイト 3 アルミニウムステアレート 2 ソルビタンセスキオレート 1 流動パラフイン 5 カルナウバワツクス 1 セレシンB 2 マイクロクリスタリンワツクス 3 マイカ 20 タルク 10 群青 10 酸化鉄赤 3 香料 適量 耐水性アイシヤドウで、塗布時は滑らかにの
び、揮散後の残留物は、化粧くずれしにくい。 又、本発明に使用する一連の有機シリコン化合
物は、公知の低沸点炭化水素、環状または鎖状ジ
メチルポリシロキサンあるいは、テトラアルキル
シラン、ヘキサアルキルジシリルアルキレン等と
の相溶性も良好なので併用して実施する事は本発
明の主旨を逸脱するものではない。
Add 238 g of hexachlorodisilyl methylene to 200 g of ethyl ether, add 6 moles of methylmagnesium bromide, and react under hydrochloric acid acidity at 80°C for 3 hours to obtain 145 g of hexamethyldisilyl methylene. [Synthesis Example 2] Add 0.5 mol of trimethylsilylmethyllithium and 0.155 mol of dimethyldichlorosilane to 500 ml of pentane, reflux for 12 hours, and then continue heating at 90°C for 12 hours to produce octamethyltrisilylmethylene with a yield of 86%. get. Next, examples of the present invention will be shown. [Example 1] Foundation (formulation) Hexaethyldisilylmethylene 40 (parts by weight) Carnauba wax 1 Microcrystalline wax 6 Organically modified montmorillonite 2 (parts by weight) Sorbitan monooleate 1 Mica 20 Talc 10 Titanium oxide 15 Iron oxide 5 Fragrance Appropriate amount When applying the obtained foundation,
It spreads smoothly and the hexaethyldisilylmethylene evaporates in a few minutes. After that, it feels refreshing and adheres closely to the skin, making it difficult for makeup to come off, and it is also water resistant so it won't come off even when bathing in the sea. [Example 2] Mascara (formulation) Hexamethyldisilylmethylene 52 (parts by weight) Carnauba wax 5 Candelilla wax 3 Microcrystalline wax 9 Cholesterol 1 Sorbitan monostearate 1 Dialkylditallow ammonium cellulose derivative 3 Aluminum star Rate 1 Purified water 5 Talc 8 Black iron oxide 12 Fragrance Appropriate amount A mascara that has no drawbacks of conventional oil-based mascaras, such as coloring the lower eyelids when blinking, has good makeup retention over time, and has excellent water resistance. . [Example 3] Eyeliner (formulation) Hexamethyldisilylmethylene 50 (parts by weight) Beeswax 5 Carnauba wax 3 Terpene resin 10 Organically modified bentonite 2 Cellulose derivative 5 Iron oxide black 10 Talc 5 Purified water 10 Fragrance Appropriate amount Implementation As with the mascara of Example 2, after hexamethyldisilylmethylene was volatilized, an eyeliner with excellent water resistance and oil resistance was obtained. [Example 4] Eye shadow formulation) Octamethyltrisilylmethylene 40 (parts by weight) Organically modified bentonite 3 Aluminum stearate 2 Sorbitan sesquiolate 1 Liquid paraffin 5 Carnauba wax 1 Ceresin B 2 Microcrystalline wax 3 Mica 20 Talc 10 Ultramarine 10 Iron oxide red 3 Fragrance Appropriate amount A water-resistant eye shadow that spreads smoothly when applied, and the residue after volatilization does not easily ruin your makeup. In addition, the series of organosilicon compounds used in the present invention have good compatibility with known low-boiling hydrocarbons, cyclic or chain dimethylpolysiloxane, tetraalkylsilane, hexaalkyldisilylalkylene, etc., so they can be used in combination. Such implementation does not depart from the spirit of the invention.

Claims (1)

【特許請求の範囲】 1 一般式()で示される有機シリコン化合物
の一種又は二種以上を配合した事を特徴とする化
粧料。 (ただし、式中Rは各々独立にメル基またはエ
チル基を示し、nは0または1の整数を示す。)
[Scope of Claims] 1. A cosmetic comprising one or more organic silicon compounds represented by the general formula (). (However, in the formula, R each independently represents a mel group or an ethyl group, and n represents an integer of 0 or 1.)
JP9395678A 1978-08-01 1978-08-01 Cosmetic Granted JPS5520735A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9395678A JPS5520735A (en) 1978-08-01 1978-08-01 Cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9395678A JPS5520735A (en) 1978-08-01 1978-08-01 Cosmetic

Publications (2)

Publication Number Publication Date
JPS5520735A JPS5520735A (en) 1980-02-14
JPS6143326B2 true JPS6143326B2 (en) 1986-09-26

Family

ID=14096863

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9395678A Granted JPS5520735A (en) 1978-08-01 1978-08-01 Cosmetic

Country Status (1)

Country Link
JP (1) JPS5520735A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62141829U (en) * 1986-02-28 1987-09-07
JPH01118526U (en) * 1988-02-03 1989-08-10
JPH022916U (en) * 1988-06-07 1990-01-10
JPH0256230U (en) * 1988-10-18 1990-04-24
JPH02150320U (en) * 1989-05-26 1990-12-26
JPH0320634U (en) * 1989-07-11 1991-02-28

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS606607A (en) * 1983-06-24 1985-01-14 Pola Chem Ind Inc Point makeup cosmetic
CN117425467A (en) * 2021-04-14 2024-01-19 迈图高新材料公司 Personal care compositions containing silane hydrocarbons

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62141829U (en) * 1986-02-28 1987-09-07
JPH01118526U (en) * 1988-02-03 1989-08-10
JPH022916U (en) * 1988-06-07 1990-01-10
JPH0256230U (en) * 1988-10-18 1990-04-24
JPH02150320U (en) * 1989-05-26 1990-12-26
JPH0320634U (en) * 1989-07-11 1991-02-28

Also Published As

Publication number Publication date
JPS5520735A (en) 1980-02-14

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