JPH04103508A - Oil-based clear cosmetic - Google Patents

Oil-based clear cosmetic

Info

Publication number
JPH04103508A
JPH04103508A JP21933990A JP21933990A JPH04103508A JP H04103508 A JPH04103508 A JP H04103508A JP 21933990 A JP21933990 A JP 21933990A JP 21933990 A JP21933990 A JP 21933990A JP H04103508 A JPH04103508 A JP H04103508A
Authority
JP
Japan
Prior art keywords
cosmetic
synthetic smectite
oil
cationic surfactant
surfactant
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP21933990A
Other languages
Japanese (ja)
Other versions
JP2963170B2 (en
Inventor
Masaaki Ishiwatari
正昭 石渡
Yoko Takashima
高嶋 陽子
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 JP21933990A priority Critical patent/JP2963170B2/en
Publication of JPH04103508A publication Critical patent/JPH04103508A/en
Application granted granted Critical
Publication of JP2963170B2 publication Critical patent/JP2963170B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To provide a clear cosmetic containing nonionic surfactant and a synthetic smectite modified with a cationic surfactant, having excellent usability and temperature stability, exhibiting skin-adhesivity and water-resistance owing to oil-based substrate and giving a durable make-up. CONSTITUTION:The objective oil-based clear cosmetic contains (A) 2-15wt.% of a synthetic smectite modified with a cationic surfactant and (B) 0.1-5 pts.wt. (based on 1 pt.wt. of the component A) of a nonionic surfactant. The component A can be produced e.g. by dissolving a cationic surfactant (e.g. dodecyltrimethylammonium chloride) in ion-exchanged water, adding a synthetic smectite to the solution, filtering the dispersion and drying the filter cake. The component B is preferably a surfactant having an HLB of 2-12, e.g. polyoxyethylene-added oleyl ether. The clear cosmetic is used as make-up cosmetic, hair cosmetic, foundation cosmetic, antisuntan cosmetic, etc.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、安定性、使用感に優れた新規な油性透明化粧
料に関し、さらに詳しくは、マスカラ、液状アイブロウ
等のメーキャップ化粧料、頭髪化粧料、クリーム、乳液
等の基礎化粧料、サンタンゲル、サンスクリーンゲル等
の日焼は用化粧料等に於いて、カチオン界面活性剤で変
性された合成スメクタイトと、非イオン界面活性剤を含
むことを特徴とする油性透明化粧料に関する。
[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a novel oil-based transparent cosmetic with excellent stability and ease of use. Basic cosmetics such as creams, emulsions, suntan gels, sunscreen gels, etc., contain synthetic smectite modified with cationic surfactants and nonionic surfactants. This invention relates to an oil-based transparent cosmetic characterized by:

〔従来の技術〕[Conventional technology]

近年、透明化粧料が目や皮膚に対し優しいイメージがあ
り清涼感が感じられる等の理由から用いられるようにな
ってきているか、水溶性カルボキシビニルポリマーを塩
基性の物質で中和し・た水性基剤が大部分であり、これ
らは耐水性がないため化粧くずれし易く、化粧効果か持
続しないという欠点がある。
In recent years, transparent cosmetics have been used for reasons such as being gentle on the eyes and skin and giving a refreshing feeling, or water-based cosmetics made by neutralizing water-soluble carboxyvinyl polymer with a basic substance. Most of the cosmetics are made up of base materials, which have the drawback of not being water resistant, making makeup easy to wear off, and making up effects not lasting as long.

本発明者らは上記事情に鑑み、化粧効果に優れ皮膚に対
する付着力や化粧膜の耐水性等により化粧(ずれしにく
(化粧効果が持続するといった品質特性に対する長所を
有し、しかも透明性の高い化粧料を得るべく鋭意研究を
重ねた結果、油性基剤に特定の物質を配合することによ
り目的とした化粧料が得られることを見出し本発明を完
成させるに至った。
In view of the above circumstances, the present inventors have discovered that the present inventors have excellent cosmetic effects, adhesion to the skin, water resistance of the cosmetic film, etc., which have advantages in terms of quality characteristics such as hardness to remove (maintaining the cosmetic effect), and transparency. As a result of extensive research in order to obtain a cosmetic with a high level of oxidation, the inventors discovered that the desired cosmetic could be obtained by blending a specific substance into an oily base, leading to the completion of the present invention.

〔課題を解決するための手段〕[Means to solve the problem]

すなわち本発明は、カチオン界面活性剤で変性された合
成スメクタイトと、非イオン界面活性剤を含むことを特
徴とする油性透明化粧料である。
That is, the present invention is an oil-based transparent cosmetic characterized by containing a synthetic smectite modified with a cationic surfactant and a nonionic surfactant.

尚、本発明でいう透明化粧料とは、日立カラーアナライ
ザーを用いて厚さ0.2cmのガラスセルに試料をとり
、380〜780nmの光を透過させ、セルの後に置い
た標準白色板のL値が30以上のものである。
In addition, the transparent cosmetics referred to in the present invention refer to samples taken in a 0.2 cm thick glass cell using a Hitachi color analyzer, light of 380 to 780 nm transmitted, and the L of a standard white plate placed behind the cell. The value is 30 or more.

以下、本発明の構成について記述する。The configuration of the present invention will be described below.

本発明で用いられるカチオン界面活性剤で変性させた合
成スメクタイトは、一般に、モンモリロナイト、サポナ
イト、ヘクトライト等の合成によって得られるスメクタ
イト属に属する層状ケイ酸塩鉱物の結晶層間に介在する
交換性カチオンをカチオン界面活性剤で置換したもので
あり、例えばイオン交換水にカチオン界面活性剤を溶解
させその水溶液に合成スメクタイトを加え分散後濾過お
よび乾燥させるというような方法で製造される。
The synthetic smectite modified with a cationic surfactant used in the present invention generally contains exchangeable cations interposed between crystal layers of layered silicate minerals belonging to the genus smectite obtained by synthesis of montmorillonite, saponite, hectorite, etc. It is substituted with a cationic surfactant, and is produced by, for example, dissolving the cationic surfactant in ion-exchanged water, adding synthetic smectite to the aqueous solution, dispersing it, and then filtering and drying it.

カチオン界面活性剤としては、たとえば次の一般式(1
)(2)(3)で表されるものか挙げられる。
As a cationic surfactant, for example, the following general formula (1
)(2)(3).

(式中、R1は炭素数10〜22のアルキル基またはベ
ンジル基、R7はメチル基または炭素数IO〜22のア
ルキル基、R3とR4は炭素数l〜3のアルキル基また
はヒドロキシアルキル基、Xはハロケン原子またはメチ
ルサルフェート残基等を表す。) [R3」 (式中、Xは窒素またはリン、Yは硫黄、Mは塩素イオ
ン、臭素イオン、ヨウ素イオン、亜硝酸イオン、ヒドロ
キシルイオン、酢酸イオン、メチル硫酸イオンまたはこ
れらの組合せであり、R1は置換基を有し、または有し
ない炭素数1〜30の炭化水素基、R2、Rs 、R4
は少な(とも1個がプロピレンオキサイド鎖(以下PO
鎖と省略する)および/またはエチレンオキサイド鎖(
以下EO鎖と省略する)を有し、末端に水素または置換
基を有し、または有しない炭素数1〜30の炭化水素基
をもち、残りのRは同一または異なった置換基を有し、
または有しない炭素数1〜30の炭化水素基である。) 一般式(1)で表されるものとしては、例えばドデシル
トリメチルアンモニウムクロリド、テトラデシルトリメ
チルアンモニウムクロリド、ヘキサデシルトリメチルア
ンモニウムクロリド、オクタデシルトリメチルアンモニ
ウムクロリド、アラキルトリメチルアンモニウムクロリ
ド、テトラデシルジメチルエチルアンモニウムクロリド
、ヘキサデシルジメチルエチルアンモニウムクロリド、
オクタデシルジメチルエチルアンモニウムクロリド、ア
ラキルジメチルエチルアンモニウムクロリド、ジオクタ
デシルジメチルアンモニウムクロリド、ジオクタデシル
ジメチルアンモニウムクロリド、ジオクタデシルジメチ
ルアンモニウムクロリド、ベンジルテトラデシルジメチ
ルアンモニウムクロリド、ベンジルヘキサデシルジメチ
ルアンモニウムクロリド、ベンジルオクタデシルジメチ
ルアンモニウムクロリド、および相当するプロミド等、
さらにジヘキサデシルプロピルエチルアンモニウムメチ
ルサルフエート等が挙げられる。
(In the formula, R1 is an alkyl group having 10 to 22 carbon atoms or a benzyl group, R7 is a methyl group or an alkyl group having IO to 22 carbon atoms, R3 and R4 are an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group, represents a halogen atom or a methyl sulfate residue, etc.) [R3'' (wherein, , methyl sulfate ion, or a combination thereof, R1 is a hydrocarbon group having 1 to 30 carbon atoms with or without a substituent, R2, Rs, R4
is small (in each case one is a propylene oxide chain (hereinafter PO
chain) and/or ethylene oxide chain (abbreviated as
(hereinafter abbreviated as EO chain), has a hydrocarbon group having 1 to 30 carbon atoms with or without hydrogen or a substituent at the terminal, and the remaining R has the same or different substituents,
or a hydrocarbon group having 1 to 30 carbon atoms. ) Examples of those represented by the general formula (1) include dodecyltrimethylammonium chloride, tetradecyltrimethylammonium chloride, hexadecyltrimethylammonium chloride, octadecyltrimethylammonium chloride, aracyltrimethylammonium chloride, tetradecyldimethylethylammonium chloride, hexadecyldimethylethylammonium chloride,
Octadecyldimethylethylammonium chloride, Arakyldimethylethylammonium chloride, Dioctadecyldimethylammonium chloride, Dioctadecyldimethylammonium chloride, Dioctadecyldimethylammonium chloride, Benzyltetradecyldimethylammonium chloride, Benzylhexadecyldimethylammonium chloride, Benzyloctadecyldimethylammonium chloride , and the corresponding promids, etc.
Further examples include dihexadecylpropylethylammonium methyl sulfate.

一般式(2)(3)で表されるものとしては、例えば、
次の(A)(B)(C)(D)(E)等が挙げられる。
Examples of those represented by general formulas (2) and (3) include:
Examples include the following (A), (B), (C), (D), and (E).

本発明で用いられる合成スメクタイトとしては、例えば
市販品ではスメクトン(クニミネ工業社製)、ラポナイ
ト(ラポルテ社製)、フッ素四ケイ素雲母(トピーエ業
社製)等がある。
Examples of the synthetic smectite used in the present invention include commercially available products such as smectone (manufactured by Kunimine Industries), laponite (manufactured by Laporte), and fluorotetrasilicon mica (manufactured by Topie Industries).

合成スメクタイトのカチオン変成率は特に限定されない
が、合成スメクタイトに対してカチオン界面活性剤を9
0〜11Oミリ当量用いるのが好ましい。
The cationic conversion rate of synthetic smectite is not particularly limited, but if cationic surfactant is added to synthetic smectite at
Preferably, 0 to 110 milliequivalents are used.

本発明で用いられるカチオン界面活性剤で変性させた合
成スメクタイトの配合量は本発明の油性透明化粧料全量
中0.5〜20重量%が好ましく、更に好ましくは2〜
15重量%である。0.5重量%未満では保存安定性が
悪<、20重量%を超えるとべたつき、使用感が悪くな
る。
The amount of the synthetic smectite modified with a cationic surfactant used in the present invention is preferably 0.5 to 20% by weight, more preferably 2 to 20% by weight based on the total amount of the oil-based transparent cosmetic of the present invention.
It is 15% by weight. If it is less than 0.5% by weight, the storage stability will be poor, and if it exceeds 20% by weight, it will be sticky and have a poor feel when used.

本発明で用いられる非イオン界面活性剤はHLB値(注
1)が1−16の範囲内のものが良く、2〜12のもの
が更に好適である。例示すれば、ポリオキシエチレン付
加(以下POEと略す。)オレイルエーテル、POEス
テアリルエーテル、POEラウリルエーテル、POEア
ルキルフェニルエーテル、POEベヘニルエーテル、P
OEデシルペンタデシルエーテル、FOE2−オクチル
デシルエーテル等のエーテル型活性剤、およびPOE硬
化ヒマシ油、POE脂肪酸モノエステル、POE脂肪酸
ジエステル、POEソルヒタン鮨肪酸エステル等のエス
テル型活性剤、更にPOEクリセリルモノイソステアレ
ート、POEクリセリルトリイソステアレート、POE
クリセリルトリイソステアレート、POE硬化硬化ヒマ
シリトリイソステアレートエーテルエステル型活性剤等
のエチレンエキシト付加型界面活性剤、およびデカクリ
セリルテトラオレート、ヘキサクリセリルトリイソステ
アレート、テトラクリセリルジイソステアレート、ジグ
リセリルジイソステアレート、等のポリグリセリン脂肪
酸エステル、クリセリルモノステアレート、クリセリル
モノイソステアレート、グリセリルリモノオレート等の
グリセリン脂肪酸エステル、等の多価アルコール脂肪酸
エステル型界面活性剤、ポリエキシアルキレン変性オル
ガノポリシロキサン、ラウロイルグルタミン酸POEオ
クチルドデシルエーテルジエステル等が挙げられる。こ
れらの中で、POE (2〜lOモル付加)オレイルエ
ーテル、FOE(10〜25モル付加)硬化ヒマシ油ト
リイソステアレート、POE (6〜20モル付加)オ
レイン酸ジエステル、POE (3〜15モル付加)硬
化ヒマシ油モノイソステアレート、ラウロイルグルタミ
ン酸POE (2〜10モル付加)オクチルドデシルエ
ーテルジエステル、POE変性オルガノポリシロキサン
等が特に好ましい。非イオン界面活性剤の配合量はカチ
オン界面活性剤で変性されたスメクタイトに対し、重量
比で0.1倍〜5倍が好ましく0.1倍未満では透明性
が充分でなく、5倍を超えると保存安定性が悪くなる。
The nonionic surfactant used in the present invention preferably has an HLB value (Note 1) within the range of 1-16, more preferably 2-12. Examples include polyoxyethylene addition (hereinafter abbreviated as POE) oleyl ether, POE stearyl ether, POE lauryl ether, POE alkylphenyl ether, POE behenyl ether, POE
Ether type activators such as OE decyl pentadecyl ether and FOE 2-octyl decyl ether, and ester type activators such as POE hydrogenated castor oil, POE fatty acid monoester, POE fatty acid diester, POE solhitan sushi fatty acid ester, and POE chryceryl. Monoisostearate, POE Chryceryl triisostearate, POE
Ethylene excito addition type surfactants such as chryceryl triisostearate, POE cured castor triisostearate ether ester type active agents, and decacryceryl tetraoleate, hexacryceryl triisostearate, tetracryceryl diiso Polyglycerin fatty acid esters such as stearate and diglyceryl diisostearate, glycerin fatty acid esters such as chryceryl monostearate, chryceryl monoisostearate, and glyceryl limonoleate, and polyhydric alcohol fatty acid ester type surfactants. agent, polyexyalkylene-modified organopolysiloxane, lauroylglutamic acid POE octyl dodecyl ether diester, and the like. Among these, POE (2-10 mol added) oleyl ether, FOE (10-25 mol added) hydrogenated castor oil triisostearate, POE (6-20 mol added) oleic acid diester, POE (3-15 mol added) Particularly preferred are hydrogenated castor oil monoisostearate (addition), lauroyl glutamic acid POE (addition of 2 to 10 moles) octyl dodecyl ether diester, POE-modified organopolysiloxane, and the like. The blending amount of the nonionic surfactant is preferably 0.1 to 5 times the weight of smectite modified with a cationic surfactant, and less than 0.1 times the transparency is insufficient, and more than 5 times the weight. and storage stability deteriorates.

(注1)非イオン界面活性剤のHLB値は、下式の周上
式により算出される。
(Note 1) The HLB value of a nonionic surfactant is calculated using the following equation.

Mw HLB= 7 +11.7  log O Mw:界面活性剤の親水基の分子量 M○:界面活性剤の親油基の分子量 本発明に係る油性透明化粧料において、化粧効果を持続
させるためには油性基剤を用いることか必要である。
Mw HLB= 7 +11.7 log O Mw: Molecular weight of the hydrophilic group of the surfactant M○: Molecular weight of the lipophilic group of the surfactant In the oil-based transparent cosmetic according to the present invention, in order to maintain the cosmetic effect, the oil-based It is necessary to use a base.

本発明に用いる油分は化粧料で用いられる一般的な油分
が用いることができ、その範囲も極性油から非極性油ま
で幅広く用いることができる。例えば、流動パラフィン
、スクヮラン、イソパラフィン、分岐鎖状軽パラフィン
等の炭化水素油、イソプロピルミリステート、セチルイ
ソオクタノエート、グリセリルトリオクタノエート等の
エステル油、デカメチルペンタシロキサン、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等のシリ
コーン油、ワセリン、マイクロクリスタリンワックス、
ラノリン、ラノリン誘導体等のワックス等が挙げられる
The oil used in the present invention can be any oil commonly used in cosmetics, and can be used in a wide range from polar oils to non-polar oils. For example, hydrocarbon oils such as liquid paraffin, squalane, isoparaffin, and branched light paraffins, ester oils such as isopropyl myristate, cetyl isooctanoate, and glyceryl trioctanoate, decamethylpentasiloxane, dimethylpolysiloxane, and methyl Silicone oil such as phenylpolysiloxane, vaseline, microcrystalline wax,
Waxes such as lanolin and lanolin derivatives are included.

本発明の油性透明化粧料には、必要に応じて有機シリコ
ーン樹脂、デキストリン脂肪酸エステル、アルミニウム
ステアレート、庶糖脂肪酸エステル等のゲル化剤、水、
エタノール、イソプロパツール等の低級アルコール、1
3ブチレンクリコール、プロピレングリコール、ジプロ
ピレングリコール、クリセリン、ソルビトール等の多価
アルコール、紫外線吸収剤、防腐剤、薬剤、香料、色素
、陰イオン界面活性剤等を配合することもできる。
The oil-based transparent cosmetic of the present invention may optionally contain an organic silicone resin, a gelling agent such as dextrin fatty acid ester, aluminum stearate, or sucrose fatty acid ester, water,
Lower alcohols such as ethanol and isopropanol, 1
Polyhydric alcohols such as 3-butylene glycol, propylene glycol, dipropylene glycol, chrycerin, and sorbitol, ultraviolet absorbers, preservatives, drugs, fragrances, pigments, anionic surfactants, and the like can also be blended.

もちろん、これらは本発明の目的を損なわない質的、量
的な条件下で使用されなければならない〔実施例〕 次に実施例をあげて本発明を更に詳細に説明する。本発
明はこれにより限定されるものではない。配合量は重量
%である。実施例に先立ち、効果、試験方法および評価
方法について延べる。
Of course, these must be used under qualitative and quantitative conditions that do not impair the purpose of the present invention. [Examples] Next, the present invention will be explained in more detail with reference to Examples. The present invention is not limited thereby. The blending amount is in weight%. Prior to examples, effects, test methods, and evaluation methods will be described.

透明性 各試料を厚さ 0.2cmのがラスセルにとり、日立カ
ラーアナライザーを用いて380〜780nmの光りを
透過させ、セルの後に置いた標準白色板のし値を測定し
た。
Transparency Each sample was placed in a glass cell with a thickness of 0.2 cm, and a Hitachi color analyzer was used to transmit light of 380 to 780 nm, and the threshold value of a standard white plate placed behind the cell was measured.

化粧持ち テスターが実際に化粧料を塗布して、2時間運動した後
、化粧効果の持続性について官能評価した。
Makeup durability testers actually applied the cosmetics, exercised for 2 hours, and then conducted a sensory evaluation of the durability of the makeup effect.

◎、化粧効果が持続した ○・化粧効果がやや持続した △;化粧効果がほとんど持続しない ×:化粧効果が全く持続しない 使用性(さっばりさ) テスターが実際に化粧料を塗布して、使用時のさっばり
さについて官能評価した。
◎, the makeup effect lasted ○, the makeup effect lasted a little △; the makeup effect hardly lasted ×: the makeup effect did not last at all Usability (lightness) The tester actually applied the cosmetic and used it. A sensory evaluation was conducted regarding the lightness of time.

◎ 非常に良好 ○ 良好 △、やや不良 ×、不良 保存安定性 0℃、室温、500Cに化粧料を放置して、−カ月経時
後の分離について評価した。
◎ Very good ◎ Good △, Slightly poor ×, Poor Storage stability The cosmetics were left at 0°C, room temperature, and 500C, and separation after - months was evaluated.

◎:非常に良好 ○:良好 △:やや不良 ×:不良 実施例1   捷用化粧料 ■イソパラフィン            71・■有
機シリコーン樹脂          2゜■ジメチル
ジステアリルアンモニウム クロリド変性合成スルフタイト     6(合成スメ
クタイトの商品名: スメクタイトSA:クニミネ工業社製)$POE(5モ
ル)ラウリルエーテル (商品名・エマレックス7o5゜ 日本エマルンヨンKK社製)        3(合成
スメクタイトの変性方法) 合成スメクタイトは以下の方法によりカチオン変性させ
た。
◎: Very good ○: Good △: Slightly poor ×: Poor Example 1 Cosmetics for cleaning ■Isoparaffin 71・■Organic silicone resin 2゜■Dimethyl distearyl ammonium chloride modified synthetic sulftite 6 (Product name of synthetic smectite: Smectite SA: manufactured by Kunimine Kogyo Co., Ltd.) $POE (5 mol) lauryl ether (trade name: Emmalex 7o5゜ manufactured by Nippon Emaruyon KK Co., Ltd.) 3 (Modification method of synthetic smectite) Synthetic smectite was cationically modified by the following method.

(1)  イオン交換水2000gに合成スメクタイト
50gを室温にて分散させた(ホモミキサー6゜00r
pm、10分間)。
(1) 50 g of synthetic smectite was dispersed in 2000 g of ion-exchanged water at room temperature (Homomixer 6°00r
pm, 10 minutes).

(2)  イオン交換水400gにカチオン界面活性剤
32.52gを80〜90℃にて加熱、溶解させた。
(2) 32.52 g of a cationic surfactant was dissolved in 400 g of ion-exchanged water by heating at 80 to 90°C.

(3)  +1+に(2)を混合し、60〜70℃にて
分散しカチオン交換した(ホモミキサー6000rpm
(3) +1+ was mixed with (2), dispersed at 60 to 70°C, and cation exchanged (Homo mixer 6000 rpm)
.

10分間)。10 minutes).

(41(31を濾過し、固形物をイオン交換水を用いて
2回洗浄した。
(41 (31) was filtered and the solid was washed twice with ion-exchanged water.

(51+4+をニーグー乾燥して、カチオン界面活性剤
で変性した合成スメクタイトを得た。
(51+4+ was dried in Nigu to obtain a synthetic smectite modified with a cationic surfactant.

(製法) ■〜■を溶解、混合し、ホモデイスパーにて均一に攪拌
し捷用化粧料を得た。
(Manufacturing method) ① to ③ were dissolved and mixed, and the mixture was uniformly stirred in a homodisper to obtain a cosmetic for mixing.

比較例1 捷毛用化粧料 ■カルボキシビニルポリマー (商品名・カーホポール94I) ■2−アミノー2−メチルプロパツール■デキストリン 0.5 0.3 (商品名、ソルブルスターチ#I6)  6.0■ヘキ
サメタリン酸ナトリウム    0.05■精製水  
            86.05■1,3−ブチレ
ングリコール      2,0■エタノール    
         5.0■メチルパラベン     
     0.1(製法) ■〜■を溶解、混合し、ホモデイスパーにて均一に攪拌
し時用化粧料を得た。
Comparative Example 1 Cosmetics for curling hair ■Carboxyvinyl polymer (product name: Carhopol 94I) ■2-Amino-2-methylpropanol ■Dextrin 0.5 0.3 (product name: soluble starch #I6) 6.0■ Sodium hexametaphosphate 0.05■Purified water
86.05■1,3-butylene glycol 2,0■Ethanol
5.0■ Methylparaben
0.1 (Production method) ① to ③ were dissolved and mixed, and the mixture was uniformly stirred in a homodisper to obtain an occasional cosmetic.

実施例1と比較例1を前記の方法で評価した結果を表−
1に示す。
The results of evaluating Example 1 and Comparative Example 1 using the above method are shown in the table below.
Shown in 1.

表−1から明らかなように実施例1の吐用化粧料は透明
性に優れ、かつ化粧効果の持続する睦月化粧料であるこ
とが確認された。
As is clear from Table 1, the emetic cosmetic of Example 1 was confirmed to have excellent transparency and a long-lasting cosmetic effect.

表 ■ 実−1 比−1 透  明  性 (L値) 使 用 性(さっばりさ) ◎・ ◎ 化粧持ち ◎  、  × 保存安定性 ◎     C 実施例2〜4比較例2.3捷用化粧料 表−1に示す処方により捷用化粧料を製造し、それぞれ
について評価した。
Table ■ Real-1 Ratio-1 Transparency (L value) Usability (lightness) ◎・ ◎ Makeup durability ◎ , × Storage stability ◎ C Examples 2 to 4 Comparative examples 2.3 Cosmetics for washing Cosmetics for washing were produced according to the formulations shown in Table 1, and each was evaluated.

(合成スメクタイトの変性方法) 各実施例、比較例で用いた合成スメクタイトは以下の方
法によりカチオン変性させた。
(Modification method of synthetic smectite) The synthetic smectite used in each example and comparative example was cationically modified by the following method.

(1)イオン交換水2000gに合成スメクタイト50
gを室温にて分散させた(ホモミキサー6000rpm
、10分間)。
(1) Synthetic smectite 50 in 2000g of ion-exchanged water
g was dispersed at room temperature (Homo mixer 6000 rpm
, 10 minutes).

(2)  イオン交換水400gにカチオン界面活性剤
27.87gを80〜90℃にて加熱、溶解させた。
(2) 27.87 g of a cationic surfactant was dissolved in 400 g of ion-exchanged water by heating at 80 to 90°C.

(31(1)に(2)を混合し、60〜70℃にて分散
しカチオン交換した(ホモミキサー6000rpm。
(31 (1) and (2) were mixed, dispersed at 60 to 70°C, and cation exchanged (Homomixer 6000 rpm).

10分間)。10 minutes).

(4)  (3)を濾過し、固形物をイオン交換水を用
いて2回洗浄した。
(4) (3) was filtered, and the solid was washed twice with ion-exchanged water.

(5)  f4)をニーダ−乾燥して、カチオン界面活
性剤で変性した合成スメクタイトを得た。
(5) f4) was kneaded and dried to obtain a synthetic smectite modified with a cationic surfactant.

(製法) ■〜■を溶解、混合し、ホモデイスパーにて均一に攪拌
し時用化粧料を得た。
(Manufacturing method) ① to ③ were dissolved and mixed, and stirred uniformly in a homodisper to obtain an occasional cosmetic.

表−2から明らかなように実施例2〜4の時用化粧料は
透明性に優れ、さっばりとした使用感触で保存安定性の
良い時用化粧料であることが確認された。
As is clear from Table 2, it was confirmed that the occasion cosmetics of Examples 2 to 4 were excellent in transparency, had a light feel on use, and had good storage stability.

表−2 実施例5〜8  比較例4〜6  頭髪化粧料表−3に
示す処方により頭髪化粧料を製造し、それぞれについて
評価した。
Table 2 Examples 5 to 8 Comparative Examples 4 to 6 Hair Cosmetics Hair cosmetics were produced according to the formulations shown in Table 3, and each was evaluated.

(合成スメクタイトの変性方法) 各実施例、比較例でもちいた合成スメクタイトは実施例
Iで用いたものと同様の方法によりカチオン変性させた
(Modification method of synthetic smectite) The synthetic smectite used in each example and comparative example was cationically modified by the same method as that used in Example I.

(製法) ■・〜■・を加熱溶解、混合し、この中に別に■〜■を
溶解したものを加えホモデイスパーにて均一に攪拌した
後冷却して頭髪化粧料を得た。
(Manufacturing method) ① to ② were heated and dissolved and mixed, to which separately dissolved ① to ② was added, stirred uniformly in a homodisper, and then cooled to obtain a hair cosmetic.

表−3から明らかなように実施例5〜8の頭髪化粧料は
透明性に優れ、さっばりした使用感触で保存安定性の良
い頭髪化粧料であることが確認された。
As is clear from Table 3, it was confirmed that the hair cosmetics of Examples 5 to 8 were excellent in transparency, had a light feeling on use, and had good storage stability.

実施例9           サンタンゲル表−4に
示す処方により、サンクンケルを製造し評価した。
Example 9 Sun Kungel was manufactured and evaluated according to the formulation shown in Santangel Table-4.

(合成スメクタイトの変性方法) 合成スメクタイトは以下の方法によりカチオン変性させ
た。
(Modification method of synthetic smectite) Synthetic smectite was cationically modified by the following method.

(1)  イオン交換水2000gに合成スメクタイト
50gを室温にて分散させた(ホモミキサー6000r
pm、10分間)。
(1) 50 g of synthetic smectite was dispersed in 2000 g of ion-exchanged water at room temperature (Homomixer 6000r
pm, 10 minutes).

(2)  イオン交換水400gにカチオン界面活性剤
30.97gを80〜90℃にて加熱溶解させた+3)
  (1)に(2)を混合し、60〜70°Cにて分散
させカチオン交換した(ホモミキサー6000rpm、
10分間)。
(2) 30.97 g of cationic surfactant was heated and dissolved in 400 g of ion-exchanged water at 80 to 90°C +3)
(2) was mixed with (1), dispersed at 60 to 70°C, and cation exchanged (Homo mixer 6000 rpm,
10 minutes).

(4)  (3’を濾過し、固形物をイオン交換水を用
いて2回洗浄した。
(4) (3' was filtered and the solid was washed twice with ion-exchanged water.

(5)  (4)をイオン交換水2500gに室温にて
再分散させ、入口温度を250℃、出口温度を1O00
Cに設定したスプレードライを用いて乾燥して、カチオ
ン界面活性剤で変性した合成スメクタイトを得た。
(5) Redisperse (4) in 2500g of ion-exchanged water at room temperature, with an inlet temperature of 250℃ and an outlet temperature of 1000℃.
It was dried using a spray dryer set to C to obtain a synthetic smectite modified with a cationic surfactant.

(製法) ■〜■を加熱溶解、混合し、この中に別に■〜[相]を
溶解したものを加えホモデイスパーにて攪拌した後冷却
してサンタンケルを得た。
(Manufacturing method) ① to ③ were dissolved and mixed by heating, and to this, separately dissolved ③ to [phase] was added, stirred in a homodisper, and then cooled to obtain Santankel.

表−4から明らかなように実施例9のサンタンゲルは透
明性に優れ、さっばりした使用感触で保存安定性の良い
サンタンゲルであることが確認された。
As is clear from Table 4, it was confirmed that the Santan gel of Example 9 was excellent in transparency, had a light feel during use, and had good storage stability.

(以下余白) 〔発明の効果〕 本発明の油性透明化粧料は、容器に入れた状態でも透明
感があり、見た目の清涼感が感じられるものである。ま
た、使用性、温度安定性といった品質特性も良好であり
、油性基剤なため皮膚に対する付着力があり耐水性があ
るので、化粧くずれしに(く化粧効果が持続するという
効果かある。
(The following is a blank space) [Effects of the Invention] The oil-based transparent cosmetic of the present invention has a transparent feel even when placed in a container, and has a refreshing appearance. In addition, it has good quality characteristics such as ease of use and temperature stability, and since it is an oily base, it has strong adhesion to the skin and is water resistant, so it has the effect of preventing makeup from coming off and providing a long-lasting makeup effect.

特許出願人 株式会社 資 生 堂Patent applicant: Shiseido Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] (1)カチオン界面活性剤で変性された合成スメクタイ
トと、非イオン界面活性剤を含むことを特徴とする油性
透明化粧料。
(1) An oil-based transparent cosmetic comprising synthetic smectite modified with a cationic surfactant and a nonionic surfactant.
JP21933990A 1990-08-21 1990-08-21 Oily transparent cosmetic Expired - Fee Related JP2963170B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21933990A JP2963170B2 (en) 1990-08-21 1990-08-21 Oily transparent cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21933990A JP2963170B2 (en) 1990-08-21 1990-08-21 Oily transparent cosmetic

Publications (2)

Publication Number Publication Date
JPH04103508A true JPH04103508A (en) 1992-04-06
JP2963170B2 JP2963170B2 (en) 1999-10-12

Family

ID=16733908

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21933990A Expired - Fee Related JP2963170B2 (en) 1990-08-21 1990-08-21 Oily transparent cosmetic

Country Status (1)

Country Link
JP (1) JP2963170B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0988019A1 (en) * 1997-05-09 2000-03-29 Avon Products, Inc. Cosmetic compositions containing smectite gels
JP2008044868A (en) * 2006-08-11 2008-02-28 Shiseido Co Ltd Gel-like composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0988019A1 (en) * 1997-05-09 2000-03-29 Avon Products, Inc. Cosmetic compositions containing smectite gels
EP0988019A4 (en) * 1997-05-09 2005-01-05 Avon Prod Inc Cosmetic compositions containing smectite gels
JP2008266351A (en) * 1997-05-09 2008-11-06 Avon Products Inc Method for producing cosmetic composition containing gel
JP2008044868A (en) * 2006-08-11 2008-02-28 Shiseido Co Ltd Gel-like composition

Also Published As

Publication number Publication date
JP2963170B2 (en) 1999-10-12

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