JP3120162B2 - Manufacturing method of oily makeup cosmetics - Google Patents

Manufacturing method of oily makeup cosmetics

Info

Publication number
JP3120162B2
JP3120162B2 JP04184317A JP18431792A JP3120162B2 JP 3120162 B2 JP3120162 B2 JP 3120162B2 JP 04184317 A JP04184317 A JP 04184317A JP 18431792 A JP18431792 A JP 18431792A JP 3120162 B2 JP3120162 B2 JP 3120162B2
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JP
Japan
Prior art keywords
oily
pigment
dispersant
fatty acid
ester
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 - Lifetime
Application number
JP04184317A
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Japanese (ja)
Other versions
JPH05331023A (en
Inventor
嘉彦 高瀬
暢之 青井
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.)
Taiyo Kagaku KK
Original Assignee
Taiyo Kagaku KK
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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明はアイシャドウ,ファンデ
−ション,マニキュア及び口紅等の無機顔料を配合した
油性メ−クアップ化粧料の製造法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing an oily makeup cosmetic containing an inorganic pigment such as eyeshadow, foundation, nail polish and lipstick.

【0002】[0002]

【従来の技術】一般にタルク,雲母,二酸化チタン,カ
オリン等の無機顔料は、水酸基のような親水性官能基や
吸着水分等の存在によりその表面の性質は極めて強い親
水性を示し、有機化合物や有機高分子化合物からなる油
性基材との親和力は弱い。そのため油性メ−クアップ化
粧料の製造において、無機顔料の油性基材への分散性が
悪く、撹拌混和する際に著しく増粘して取扱困難になっ
たり、無機顔料の分散不良による製品の品質劣化等の問
題が起こる。この為従来技術では油性基材と無機顔料の
親和力を増す為分散媒である有機化合物や有機高分子化
合物等の油性基材に極性基を導入してイオン結合性を持
たせたり、分散質である無機顔料を表面処理してそのイ
オン結合性を弱くするもしくは共有結合性を持たせる方
法が取られている。また従来から無機顔料の油性基剤へ
の分散剤として、脂肪酸モノグリセリド,ソルビタン脂
肪酸エステル,脂肪酸アルキロ−ルアミド等の界面活性
剤や、ラノリン脂肪酸イソプロピル,ラウリン酸ヘキシ
ル,イソオクタン酸セチル等の脂肪酸エステルが使用さ
れている。
2. Description of the Related Art In general, inorganic pigments such as talc, mica, titanium dioxide and kaolin exhibit extremely strong hydrophilic properties due to the presence of hydrophilic functional groups such as hydroxyl groups and adsorbed moisture. The affinity with the oil-based substrate made of an organic polymer compound is weak. Therefore, in the production of oily makeup cosmetics, the dispersibility of the inorganic pigment in the oily base material is poor, and the viscosity is greatly increased during stirring and mixing, which makes it difficult to handle, or the quality of the product is deteriorated due to poor dispersion of the inorganic pigment. And other problems occur. For this reason, in the prior art, in order to increase the affinity between the oily base material and the inorganic pigment, a polar group is introduced into the oily base material such as an organic compound or an organic polymer compound as a dispersion medium so as to have an ionic bond, A method has been adopted in which a certain inorganic pigment is subjected to surface treatment to weaken its ionic bond or impart covalent bond. Conventionally, surfactants such as fatty acid monoglyceride, sorbitan fatty acid ester and fatty acid alkyl amide, and fatty acid esters such as isopropyl lanolin fatty acid, hexyl laurate, and cetyl isooctanoate have been used as dispersants for oily bases of inorganic pigments. Have been.

【0003】[0003]

【発明が解決しようとする課題】しかし、これらの方法
は増粘による取扱の問題や、分散不良の問題を完全に解
決することが出来ず若干の改良をするに留まっており、
また複雑な工程と高価な設備を必要とする為極めて不経
済である欠点を有する。
However, these methods cannot completely solve the problem of handling due to thickening and the problem of poor dispersion, so that only a slight improvement is made.
Further, it has a drawback that it is extremely uneconomical because it requires complicated steps and expensive equipment.

【0004】[0004]

【問題を解決するための手段】本発明者らは上記欠点に
鑑み、鋭意研究の結果本発明に至った。即ち、本発明は
縮合度が少なくとも2以上の縮合ヒドロキシ脂肪酸と多
価アルコ−ルとのエステルからなる分散剤を必須成分と
して構成される油性メ−クアップ化粧料の製造法であ
る。本発明のヒドロキシ脂肪酸とは、例えばリシノレイ
ン酸,12−ヒドロキシステアリン酸,ジヒドロキシス
テアリン酸等の1種もしくは2種以上の混合物が挙げら
れる。また多価アルコ−ルとは、アルカンポリオ−ル,
糖類,糖類誘導体,ポリアルカンポリオ−ル及びそれら
の2種以上の混合物が挙げられる。上記アルカンポリオ
−ルとしては、ペンタエリスリト−ル,グリセリンな
ど,糖類としてはショ糖など,糖類誘導体としては糖類
アルコ−ル,例えばソルビト−ル,マンニト−ルなど,
ポリアルカンポリオ−ルとしては、ジまたはトリペンタ
エリスリト−ル,ポリグリセリンなどを例示出来る。特
許請求の範囲で表した分散剤は種々の方法で製造するこ
とができる。例えばまずヒドロキシ脂肪酸を加熱下で縮
合させて得られた縮合ヒドロキシ脂肪酸と多価アルコ−
ルを、苛性ソ−ダ等の触媒を加えて加熱下でエステル化
する。エステル化の反応の進行は酸価,ケン化価,水酸
基価等の測定を行うことで確認することができる。
Means for Solving the Problems In view of the above-mentioned drawbacks, the present inventors have made intensive studies and arrived at the present invention. That is, the present invention is a process for producing an oily makeup cosmetic comprising, as an essential component, a dispersant comprising an ester of a condensed hydroxy fatty acid having a degree of condensation of at least 2 and a polyhydric alcohol. Examples of the hydroxy fatty acid of the present invention include one or a mixture of two or more of ricinoleic acid, 12-hydroxystearic acid, and dihydroxystearic acid. In addition, polyvalent alcohol is alkanepolyol,
Examples include saccharides, saccharide derivatives, polyalkanepolyols, and mixtures of two or more thereof. Examples of the alkane polyols include pentaerythritol and glycerin, saccharides such as sucrose, and saccharide derivatives such as saccharide alcohols such as sorbitol and mannitol.
Examples of the polyalkane polyol include di- or tripentaerythritol and polyglycerin. The dispersants described in the claims can be produced by various methods. For example, a condensed hydroxy fatty acid obtained by first condensing a hydroxy fatty acid under heating and a polyhydric alcohol-
The ester is esterified under heating with the addition of a catalyst such as caustic soda. The progress of the esterification reaction can be confirmed by measuring the acid value, saponification value, hydroxyl value and the like.

【0005】本発明の油性メ−クアップ化粧料とはアイ
シャドウ,ファンデ−ション,マニキュア,口紅などの
油性基剤中に無機顔料を分散してなる化粧料である。無
機顔料とは、通常油性メ−クアップ化粧料に用いられる
顔料であれば特に限定されず例えば二酸化チタン,カオ
リン,タルク,ベントナイト,マイカ,ベンガラ,炭酸
カルシウム,ラウリン酸亜鉛,カ−ボンブラック,ステ
アリン酸亜鉛,雲母等挙げられる。これらの顔料は1種
もしくは2種以上を組み合わせて使用出来る。またタ−
ル色素等の有機顔料と併用しても何ら問題はない。油性
基剤も通常油性メ−クアップ化粧料に用いられる油性基
剤であれば特に限定されず例えば、流動パラフィン,ヒ
マシ油,ミツロウ,カルナバロウ,キャンデリラロウ,
パルミチン酸イソプロピル,ラノリンアルコ−ルオクチ
ルドデカノ−ル,液状ラノリン等挙げられる。これらの
油性基剤は1種もしくは2種以上を混合して使用でき
る。
[0005] The oily makeup cosmetic of the present invention is a cosmetic comprising an inorganic pigment dispersed in an oily base such as eyeshadow, foundation, nail polish and lipstick. The inorganic pigment is not particularly limited as long as it is a pigment which is usually used in oily makeup cosmetics. For example, titanium dioxide, kaolin, talc, bentonite, mica, red bengala, calcium carbonate, zinc laurate, carbon black, stearin Zinc acid, mica and the like. These pigments can be used alone or in combination of two or more. In addition,
There is no problem when used in combination with organic pigments such as dyes. The oily base is not particularly limited as long as it is an oily base usually used in oily makeup cosmetics. For example, liquid paraffin, castor oil, beeswax, carnauba wax, candelilla wax,
Isopropyl palmitate, lanolin alcohol octyl dodecanol, liquid lanolin and the like. These oily bases can be used alone or in combination of two or more.

【0006】本発明の分散剤の添加量は、顔料等に対し
て0.1〜100重量%、好ましくは0.1〜50重量
%である。油性基剤中における顔料の含有率は1〜90
重量%、好ましくは5〜80重量%である。本発明にお
いては、まず初めに油性基剤の1種もしくは2種以上を
必要に応じて加温溶解し、よく混合する。つぎに顔料の
1種もしくは2種以上を油性基剤中へ徐々に添加し、攪
拌混合し、分散せしめる。分散剤はこれらの工程中どこ
で添加しても良いが、好ましくは顔料を油性基剤に加え
る前に油性基剤もしくは顔料にあらかじめ添加してお
く。更に好ましくは油性基剤中にあらかじめ分散剤を添
加混合溶解しておくのが良い。分散方法は特に限定しな
いが、ホモミキサーロールミル等の攪拌装置を用い、攪
拌混合時の温度は室温〜95℃にしておく。分散後は脱気
し、必要に応じて冷却する。このように得られる本発明
化粧料は、特に制限されないが、アイシャドウ,ファン
デ−ション,口紅,マニキュア,ほお紅,アイライナ−
等として使用出来る。
The addition amount of the dispersant of the present invention is 0.1 to 100% by weight, preferably 0.1 to 50% by weight, based on the pigment or the like. The content of the pigment in the oil base is from 1 to 90.
% By weight, preferably 5 to 80% by weight. In the present invention, first, one or more kinds of oily bases are heated and dissolved, if necessary, and mixed well. Next, one or more kinds of pigments are gradually added to the oily base, mixed with stirring, and dispersed. The dispersant may be added at any point during these steps, but is preferably added to the oily base or pigment before adding the pigment to the oily base. More preferably, a dispersing agent is added and mixed and dissolved in the oil base in advance. The dispersion method is not particularly limited, but a stirring device such as a homomixer roll mill is used, and the temperature during stirring and mixing is kept at room temperature to 95 ° C. After dispersing, degas and cool if necessary. The cosmetic of the present invention obtained in this manner is not particularly limited, but includes eye shadow, foundation, lipstick, nail polish, blusher, eye liner.
Etc. can be used.

【0007】以下に製造例、実施例及び比較例を示して
本発明を具体的に説明するが、本発明がこれらによって
限定されるものではない。
Hereinafter, the present invention will be described specifically with reference to Production Examples, Examples, and Comparative Examples, but the present invention is not limited thereto.

【0008】[0008]

【実施例】【Example】

実施例1 1リットルの四つ口フラスコにリシノレイン酸600g
入れ、窒素気流下で生成水を除去しながら180℃で反
応して縮合リシノレイン酸を得た。この縮合物の酸価は
48であった。次にこの縮合リシノレイン酸350gと
トリペンタエリスリト−ル50g及び水酸化ナトリウム
0.4gを1リットルの四つ口フラスコに入れ窒素気流
下で生成水を除去しながら250℃で反応してエステル
化物を得た。このエステルの酸価は4.5であった。
Example 1 600 g of ricinoleic acid in a 1 liter four-necked flask
The reaction was carried out at 180 ° C. while removing generated water under a nitrogen stream to obtain condensed ricinoleic acid. The acid value of this condensate was 48. Next, 350 g of this condensed ricinoleic acid, 50 g of tripentaerythritol and 0.4 g of sodium hydroxide are placed in a 1-liter four-necked flask and reacted at 250 ° C. while removing generated water under a nitrogen stream to obtain an esterified product. I got The acid value of this ester was 4.5.

【0009】実施例2 実施例1で用いた縮合リシノレイン酸350gとソルビ
ト−ル36gから実施例1に準じてエステル化物を得
た。このエステルの酸価は5.0であった。
Example 2 An esterified product was obtained from 350 g of the condensed ricinoleic acid and 36 g of sorbitol used in Example 1 in the same manner as in Example 1. The acid value of this ester was 5.0.

【0010】実施例3 実施例1で用いたリシノレイン酸の代わりに12−ヒド
ロキシステアリン酸を用い,実施例1に準じてエステル
化物を得た。このエステルの酸価は5.0であった。
Example 3 An esterified product was obtained in the same manner as in Example 1 except that ricinoleic acid used in Example 1 was replaced with 12-hydroxystearic acid. The acid value of this ester was 5.0.

【0011】実施例4 下記処方にて油性軟膏型ファンデーションを調製した。 油性基剤: 流動パラフィン 24.5% パルミチン酸2−エチルヘキシル 15.0% ラノリンアルコ−ル 2.0% 酢酸ラノリン 3.0% マイクロクリスタリンワックス 7.0% オゾケライト 7.0% キャンデリラロウ 0.5% 酸化防止剤 殺菌剤 適量 分散剤: 実施例1のエステル化物 1.0% 顔料: 二酸化チタン 15.0% タルク 15.0% カオリン 6.0% 着色顔料 4.0% 香料 適量 上記処方にて油性基剤に分散剤を加えて80〜90℃に
加温して溶解させた後顔料を加えてホモミキサ−にて分
散する。脱気後,冷却し軟膏型ファンデ−ションを得
た。
Example 4 An oily ointment type foundation was prepared according to the following formulation. Oil base: liquid paraffin 24.5% 2-ethylhexyl palmitate 15.0% lanolin alcohol 2.0% lanolin acetate 3.0% microcrystalline wax 7.0% ozokerite 7.0% candelilla wax 0.0 5% Antioxidant Disinfectant Appropriate amount Dispersant: Esterified product of Example 1 1.0% Pigment: Titanium dioxide 15.0% Talc 15.0% Kaolin 6.0% Color pigment 4.0% Fragrance Appropriate amount Then, a dispersant is added to the oily base, and the mixture is heated to 80 to 90 ° C. to dissolve it. Then, the pigment is added and dispersed by a homomixer. After degassing, the mixture was cooled to obtain an ointment type foundation.

【0012】比較例1 実施例4の処方にて分散剤を加えずに軟膏型ファンデ−
ションを実施例1の方法に準じて調製した。
Comparative Example 1 An ointment type foundation was prepared according to the formulation of Example 4 without adding a dispersant.
Was prepared according to the method of Example 1.

【0013】比較例2 実施例4の処方にて、分散剤をステアリン酸モノエタノ
−ルアミドい代えて実施例1の方法に準じて軟膏型ファ
ンデ−ションを調製した。
Comparative Example 2 An ointment type foundation was prepared in the same manner as in Example 1 except that the dispersant was replaced by monoethanolamide stearate.

【0014】実施例5 下記処方にて軟膏型アイシャド−を調製した。 油性基剤: マイクロクリスタリンワックス 14.0% セレシン 7.0% アセチル化ラノリン 5.0% 流動パラフィン 31.0% イソステアリン酸セチル 13.0% 酸化防止剤 殺菌剤 適量 分散剤: 実施例2のエステル化物 2.0% 顔料: 二酸化チタン 5.0% タルク 8.0% グンジョウ 15.0% 上記処方にて油性基剤に分散剤を加え80〜90℃に加
温し溶解した後顔料を加えてホモミキサ−にて分散す
る。その後脱気し冷却を行い軟膏型アイシャド−を得
た。
Example 5 An ointment type eye shadow was prepared according to the following formulation. Oily base: microcrystalline wax 14.0% ceresin 7.0% acetylated lanolin 5.0% liquid paraffin 31.0% cetyl isostearate 13.0% antioxidant disinfectant proper amount dispersant: ester of Example 2 2.0% Pigment: Titanium dioxide 5.0% Talc 8.0% Gunjo 15.0% A dispersant is added to the oily base according to the above formulation, the mixture is heated to 80 to 90 ° C., dissolved, and then the pigment is added. Disperse with a homomixer. Thereafter, the mixture was degassed and cooled to obtain an ointment type eye shadow.

【0015】比較例3 実施例5の処方にて分散剤を加えずに実施例5に準じて
軟膏型アイシャド−を得た。
Comparative Example 3 An ointment type eye shadow was obtained in the same manner as in Example 5 except that the dispersant was not added.

【0016】比較例4 実施例5の処方にて、分散剤をソルビタンモノオレ−ト
に代えて実施例5の方法に準じて軟膏型アイシャド−を
得た。
Comparative Example 4 An ointment type eye shadow was obtained in the same manner as in Example 5 except that sorbitan monooleate was used as the dispersing agent.

【0017】実施例6 下記処方にて軟膏型ほお紅を調製した。 油性基剤:流動パラフィン 21.0% セレシン 15.0% ワセリン 40.0% ラノリン 5.0% 酸化防止剤 殺菌剤 適量 香料 適量 分散剤:実施例3 1.0% 顔料:タルク 4.0% 二酸化チタン 3.0% カオリン 5.0% ステアリン酸亜鉛 1.0% 色材 5.0% 上記処方にて油性基剤に分散剤を加え80〜90℃に加
温溶解した後ホモミキサ−にて分散し、脱気,冷却して
軟膏型ほお紅を得た。
Example 6 An ointment type blush was prepared according to the following formulation. Oil base: liquid paraffin 21.0% ceresin 15.0% vaseline 40.0% lanolin 5.0% antioxidant bactericide appropriate amount perfume appropriate amount dispersant: Example 3 1.0% pigment: talc 4.0% Titanium dioxide 3.0% Kaolin 5.0% Zinc stearate 1.0% Colorant 5.0% Add dispersant to oily base in the above formulation, heat and dissolve at 80-90 ° C, then use homomixer It was dispersed, degassed, and cooled to obtain an ointment type blusher.

【0018】比較例5 実施例6の処方にて分散剤を加えずに実施例6の方法に
準じて軟膏型ほお紅を調製した。
Comparative Example 5 An ointment type blusher was prepared in the same manner as in Example 6 except that no dispersant was added.

【0019】比較例6 実施例6の処方にて、分散剤をリシノレイン酸モノグリ
セリドに代えて実施例6の方法に準じて軟膏型ほお紅を
調製した。
Comparative Example 6 An ointment type blush was prepared in the same manner as in Example 6, except that ricinoleic acid monoglyceride was used in place of the dispersant.

【0020】試験例1 実施例4〜6、比較例1〜6の顔料分散性、肌ざわりに
ついて評価した。結果を表1に示す。
Test Example 1 Examples 4 to 6 and Comparative Examples 1 to 6 were evaluated for pigment dispersibility and texture. Table 1 shows the results.

【0002】[0002]

【表1】 [Table 1]

【0021】[0021]

【発明の効果】上記実施例,試験例で証明した様に本発
明によれば、油性基剤内に極性基を導入したり無機顔料
の表面処理など複雑で不経済な工程を行うことなく、高
品質な油性メ−クアップ化粧料が得られることは明白で
ある。
According to the present invention, as proved in the above Examples and Test Examples, a complicated and uneconomical process such as introduction of a polar group into an oily base or surface treatment of an inorganic pigment can be achieved. It is clear that a high quality oily makeup cosmetic can be obtained.

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 縮合度2以上の縮合ヒドロキシ脂肪酸
と、ペンタエリスリトール、グリセリン、ショ糖、ソル
ビトール、マンニトール、ジもしくはトリペンタエリス
リトール、及びポリグリセリンからなる群より選ばれる
1種または2種以上の多価アルコールとのエステル及び
18%以上の無機顔料を含有する実質的に水分を含まな
い油性メークアップ化粧料。
1. A condensed hydroxy fatty acid having a condensation degree of 2 or more, and one or more polyhydric acids selected from the group consisting of pentaerythritol, glycerin, sucrose, sorbitol, mannitol, di- or tripentaerythritol, and polyglycerin. A substantially water-free oily makeup cosmetic containing an ester with a polyhydric alcohol and 18% or more of an inorganic pigment.
【請求項2】 縮合度2以上の縮合ヒドロキシ脂肪酸
と、ペンタエリスリトール、グリセリン、ショ糖、ソル
ビトール、マンニトール、ジもしくはトリペンタエリス
リトール、及びポリグリセリンからなる群より選ばれる
1種または2種以上の多価アルコールとのエステルを含
有することを特徴とする油性メークアップ化粧料用無機
顔料分散剤。
2. A condensed hydroxy fatty acid having a condensation degree of 2 or more, and one or more polyhydric acids selected from the group consisting of pentaerythritol, glycerin, sucrose, sorbitol, mannitol, di- or tripentaerythritol, and polyglycerin. An inorganic pigment dispersant for oily make-up cosmetics, comprising an ester with a polyhydric alcohol.
JP04184317A 1992-05-30 1992-05-30 Manufacturing method of oily makeup cosmetics Expired - Lifetime JP3120162B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP04184317A JP3120162B2 (en) 1992-05-30 1992-05-30 Manufacturing method of oily makeup cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP04184317A JP3120162B2 (en) 1992-05-30 1992-05-30 Manufacturing method of oily makeup cosmetics

Publications (2)

Publication Number Publication Date
JPH05331023A JPH05331023A (en) 1993-12-14
JP3120162B2 true JP3120162B2 (en) 2000-12-25

Family

ID=16151223

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3120162B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0846715A (en) * 1994-07-28 1996-02-16 Murata Mach Ltd Communication terminal equipment

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6344509B1 (en) * 1994-12-22 2002-02-05 Taiyo Kagaku Co., Ltd. Thermoplastic resin compositions
WO2006080390A1 (en) 2005-01-28 2006-08-03 The Nisshin Oillio Group, Ltd. Lip cosmetic
JP5395325B2 (en) 2005-01-28 2014-01-22 日清オイリオグループ株式会社 Esterification reaction products and cosmetics
EP2639253A4 (en) * 2010-11-08 2016-11-02 Nisshin Oillio Group Ltd Esterification product and cosmetics

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62234046A (en) * 1986-04-02 1987-10-14 Nisshin Oil Mills Ltd:The Novel esterification product and cosmetic containing said product
JPS6490025A (en) * 1987-10-01 1989-04-05 Sakamoto Yakuhin Kogyo Kk Novel emulsifier
JPH0374315A (en) * 1989-08-11 1991-03-28 Nisshin Oil Mills Ltd:The Esterified product and cosmetic or external drug containing the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0846715A (en) * 1994-07-28 1996-02-16 Murata Mach Ltd Communication terminal equipment

Also Published As

Publication number Publication date
JPH05331023A (en) 1993-12-14

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