JPH0133442B2 - - Google Patents

Info

Publication number
JPH0133442B2
JPH0133442B2 JP54130182A JP13018279A JPH0133442B2 JP H0133442 B2 JPH0133442 B2 JP H0133442B2 JP 54130182 A JP54130182 A JP 54130182A JP 13018279 A JP13018279 A JP 13018279A JP H0133442 B2 JPH0133442 B2 JP H0133442B2
Authority
JP
Japan
Prior art keywords
emulsified
fatty acid
acid ester
water
stake
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
JP54130182A
Other languages
Japanese (ja)
Other versions
JPS5653608A (en
Inventor
Kunihiro Ito
Toshiaki Sugizaki
Yoshio Hagiwara
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.)
Kobayashi Kose Co Ltd
Original Assignee
Kobayashi Kose 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 Kobayashi Kose Co Ltd filed Critical Kobayashi Kose Co Ltd
Priority to JP13018279A priority Critical patent/JPS5653608A/en
Publication of JPS5653608A publication Critical patent/JPS5653608A/en
Publication of JPH0133442B2 publication Critical patent/JPH0133442B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0216Solid or semisolid forms
    • A61K8/0229Sticks
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/042Gels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • A61K8/064Water-in-oil emulsions, e.g. Water-in-silicone emulsions
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/39Derivatives containing from 2 to 10 oxyalkylene groups
    • 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
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4973Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
    • 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
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin

Description

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

本発明は改良された油中水型(W/O型)乳化
ステイツク化粧料に係り、その目的とするところ
は、肌に対しエモリエント性を有し、発汗、折れ
等がなく安定で、しかも微生物汚染のないW/O
型乳化ステイツク化粧料を提供せんとするにあ
る。 従来、乳化ステイツク化粧料としては、油性成
分を主体とする基材に、界面活性剤とグリセリ
ン、マンニツト、果糖、デンプン等の多価アルコ
ールあるいは炭水化物とからなるゲルと水を混合
して製造したもの(特開昭48−103742号);ソル
ビタンオレイン酸エステル又はジグリセリンオレ
イン酸エステルと油性物質あるいはこれと色素と
の混合物にマルチトール水溶液を加えて製造した
もの(特開昭53−127841号及び同54−49337号)
等が知られている。 これらの化粧料は、製品の安定性、保水性、折
れ強度、肌への伸びを向上させ、成型時の離型性
を改善する目的のために、その処方中に上記のよ
うな多価アルコール又は炭水化物を配合している
が、これらは微生物の汚染の原因となり、必ずし
も満足な結果は得られない。 そこで、本発明者は、W/O型乳化ステイツク
化粧料、特に界面活性剤、多価アルコール、炭水
化物の影響について鋭意研究を行つた結果、
HLB9以下の界面活性剤と水とで予めゲルを生成
し、これを油性成分中に加えて乳化を行えば、上
記多価アルコール又は炭水化物等を添加すること
なく、上記特性を具備した乳化ステイツク化粧料
が得られることを見出した。更にまた、本発明者
は上記の界面活性剤と水とのゲルに有機酸又はそ
の塩を添加すると、ゲルの安定性及び強度が向上
されると共に、W/O乳化系における緩衝作用を
示し、また防腐剤としてのグリコール類の添加が
容易になることを見出した。 本発明は斯る新知見に基いて完成されたもの
で、HLB9以下の界面活性剤、水及び有機酸又は
その塩類によつて生成されるゲルを油性成分に添
加乳化して得られるW/O型乳化ステイツク化粧
料を提供するものである。 本発明において、HLB9以下の界面活性剤とし
ては種々のものが使用されるが、例えばソルビタ
ン脂肪酸エステル、グリセリン脂肪酸エステル、
ポリオキシエチレン硬化ヒマシ油脂肪酸エステ
ル、ジグリセリン脂肪酸エステル、ポリオキシエ
チレン硬化ヒマシ油、ポリオキシエチレンアルキ
ルフエノール類等が挙げられる。これらの界面活
性剤は1種又は2種以上を組合せて使用すること
ができ、これは全組成の0.5〜10%になるように
配合するのが好ましい。 また、ゲル形成に使用する水は界面活性剤に対
して0.5〜10倍が適当である。 なお、HLBが9より大である界面活性剤を用
いた場合、水との間でゲルが生成しないので、こ
れを油性成分に添加乳化してもW/O型のエマル
ジヨンとならず、O/W型のエマルジヨンが部分
的に生成されるだけである。 そして、このようなO/W型のエマルジヨンを
用いても水をステイツク化粧料の構成基材である
油性成分(ワツクス、液状油等)にうまく配合す
ることはできず、好ましい性質を有する乳化ステ
イツク化粧料を得ることはできない。 油性成分としては、ステイツク化粧料の製造に
使用されている公知のものが使用され、例えばヒ
マシ油、オリーブ油等の油脂;木ロウ、ラノリ
ン、ミツロウ、カルナバロウ、キヤンデリラワツ
クス等のワツクス;流動パラフイン、固形パラフ
イン等の炭化水素;エステル油、高級脂肪酸等が
挙げられる。 更にまた、有機酸又はその塩類としては、例え
ばクエン酸、乳酸、ピロリドンカルボン酸及びそ
のナトリウム、カリウム等のアルカリ金属塩が挙
げられる。これらは全組成の0.05〜5%配合する
のが好ましい。 本発明のW/O型乳化ステイツク化粧料を製造
するには、まず所定量の水に界面活性剤を加えて
撹拌してゲルを生成させる。このゲルには所定量
の有機酸又はその塩類が添加される。一方、油性
成分は、これが固体の場合には加温して液状とな
し、これに上で調製したゲルを撹拌下徐々に加え
て乳化を行う。斯くして得られる乳化物を型に入
れ冷却すれば本発明の乳化ステイツク化粧料が得
られる。 尚ステイツク化粧料に通常配合される顔料、染
料、香料、防腐剤、酸化防止剤は、上記ゲル又は
油性成分の何れかに添加し配合される。そして、
従来ゲルを破壊するため配合が困難であつたプロ
ピレングリコール、1,3−ブチレングリコール
等のグリコール類を添加することができ、その結
果微生物による汚染を防止することができる。 叙上の如く、本発明のW/O型乳化ステイツク
化粧料は、その製造が極めて簡単であると共に、
安定性、保水性、折れ強度、肌への伸びにおいて
優れており、しかも微生物による汚染が少ない等
種々の利点を有するものである。 次に実施例を挙げて説明する。 実施例 1 ステイツクアイクリーム 組成: 1 流動パラフイン 51.2(重量部) 2 スクワラン 10.0 3 固形パラフイン 10.0 4 キヤンデリラワツクス 10.0 5 ラノリン 5.0 6 防腐剤 0.1 7 香 料 0.2 8 グリセロールモノオレエート 3.0 9 ピロリドンカルボン酸ソーダ 0.5 10 精製水 10.0 製法: (A) 1〜7を溶解する (B) 8に9及び10の溶液を加えゲルを生成する。 (C) BをAに添加し乳化する。これを脱気後、70
℃で成型容器に流し込み、冷却してステイツク
状にする。 実施例 2 ステイツクフアンデーシヨン 組成: 1 流動パラフイン 47.2(重量部) 2 固形パラフイン 10.0 3 シヨ糖脂肪酸エステル 5.0 4 混合顔料 15.0 5 ラノリン 5.0 6 防腐剤 0.1 7 香 料 0.5 8 ジグリセリンジイソステアレート 4.0 9 クエン酸ナトリウム 1.0 10 クエン酸 0.2 11 プロピレングリコール 2.0 12 精製水 10.0 製法: 実施例1と同様に操作してステイツクフアンデ
ーシヨンを得る。 比較例 1 ステイツクアイクリーム 組成: (重量%) 1 流動パラフイン 44.7 2 スクワラン 10.0 3 固形パラフイン 10.0 4 キヤンデリラワツクス 10.0 5 ラノリン 5.0 6 防腐剤 0.1 7 香 料 0.2 8 グリセリルモノオレエート 3.0 9 ソルビトール液(70%水溶液) 10.0 10 精製水 7.0 製法: 実施例1と同様に操作してステイツクアイクリ
ームを得る。 このものは、実施例1のステイツクアイクリー
ムにおいて、ゲルにピロリドンカルボン酸ソーダ
を加えずにソルビトールを加えたものであるが、
実施例3のものに比べ、ステイツクの構造が弱く
なり、折れ強度が弱くなつていた。また、乳化能
が劣るため、保水性が悪くなると共に軽やかな伸
びが得られず、また、外観の白度も低下した。 比較例 2 実施例1の組成からピロリドンカルボン酸ソー
ダを除き、精製水を10.5重量部とする以外は実施
例1と同様にしてステイツクアイクリーム(比較
品1)を調製した。 比較例 3 実施例2の組成からクエン酸ナトリウム及びク
エン酸を除き、精製水を11.2重量部とする以外は
実施例2と同様にしてステイツクフアンデーシヨ
ン(比較品2)を調製した。 試験例 1 実施例1のステイツクアイクリーム(本発明品
1)と比較品1について次の比較試験を行つた。 (1) 硬度変化による安定性試験 <試料> 本発明品1及び比較品1を14mmφ×37mmの円
筒形状のくり出し容器に充填成型する。これを
40℃の恒温槽に入れ、1日又は2週間保存後と
り出し、20℃の恒温槽に2時間放置する。容器
からくり出し、14mmφ×35mmの円筒にカツトし
て試料とした。 <硬度測定> レオメーターNRM−2002J(不動工業株式会
社製)〔アダプター:ピアノ線カツター、V字
ホルダー〕を用いて、レンジ500g、テーブル
上昇速度6cm/分の条件で測定した。 <結果> 3個の試料について行い、その結果を第1表
に示す。
The present invention relates to an improved water-in-oil type (W/O type) emulsion stick cosmetic, which aims to have emollient properties for the skin, be stable without sweating or breakage, and be microorganism-resistant. Contamination-free W/O
We aim to provide emulsified cosmetics. Traditionally, emulsified cosmetics have been produced by mixing water with a gel consisting of a surfactant and polyhydric alcohols such as glycerin, mannitrate, fructose, starch, or carbohydrates, in a base material mainly consisting of oily ingredients. (Japanese Patent Application Laid-Open No. 103742/1982); produced by adding an aqueous solution of maltitol to a mixture of sorbitan oleate or diglycerin oleate and an oily substance or a pigment (Japanese Patent Application Laid-open No. 127841/1984); 54-49337)
etc. are known. These cosmetics contain polyhydric alcohols such as those mentioned above in their formulations in order to improve product stability, water retention, bending strength, spreadability on the skin, and improve mold release properties during molding. Alternatively, carbohydrates are added, but these can cause microbial contamination and do not always give satisfactory results. Therefore, as a result of intensive research into the effects of W/O type emulsified cosmetics, particularly surfactants, polyhydric alcohols, and carbohydrates, the present inventor found that
If a gel is generated in advance from a surfactant with an HLB of 9 or less and water, and this gel is added to an oil-based ingredient and emulsified, an emulsified makeup with the above characteristics can be created without adding the polyhydric alcohol or carbohydrates, etc. I found that I could get a lot of money. Furthermore, the present inventor has found that when an organic acid or a salt thereof is added to the gel of the above-mentioned surfactant and water, the stability and strength of the gel are improved, and a buffering effect is exhibited in a W/O emulsion system. It has also been found that glycols can be easily added as preservatives. The present invention was completed based on this new knowledge, and it is a W/O obtained by adding and emulsifying a gel generated from a surfactant with an HLB of 9 or less, water, and an organic acid or its salts to an oily component. The present invention provides an emulsified stick cosmetic. In the present invention, various surfactants with HLB of 9 or less are used, such as sorbitan fatty acid ester, glycerin fatty acid ester,
Examples include polyoxyethylene hydrogenated castor oil fatty acid ester, diglycerin fatty acid ester, polyoxyethylene hydrogenated castor oil, and polyoxyethylene alkylphenols. These surfactants can be used alone or in combination of two or more, and are preferably blended in an amount of 0.5 to 10% of the total composition. Further, the water used for gel formation is suitably 0.5 to 10 times the surfactant. Note that when a surfactant with an HLB of greater than 9 is used, no gel is formed with water, so even if it is added to an oil component and emulsified, a W/O type emulsion will not be obtained, and an O/O type emulsion will not be formed. A W-type emulsion is only partially produced. Even if such an O/W type emulsion is used, it is not possible to properly incorporate water into the oily components (wax, liquid oil, etc.) that are the constituent base materials of static cosmetics. You can't get cosmetics. As the oily component, known ones used in the production of static cosmetics are used, such as fats and oils such as castor oil and olive oil; waxes such as wood wax, lanolin, beeswax, carnauba wax, and candelilla wax; liquid paraffin. , hydrocarbons such as solid paraffin; ester oils, higher fatty acids and the like. Furthermore, examples of organic acids or their salts include citric acid, lactic acid, pyrrolidone carboxylic acid, and their alkali metal salts such as sodium and potassium. It is preferable to mix these in an amount of 0.05 to 5% of the total composition. To produce the W/O type emulsion stake cosmetic of the present invention, a surfactant is first added to a predetermined amount of water and stirred to form a gel. A predetermined amount of organic acid or its salt is added to this gel. On the other hand, if the oily component is solid, it is heated to make it liquid, and the gel prepared above is gradually added thereto under stirring to emulsify it. The emulsion thus obtained is placed in a mold and cooled to obtain the emulsified stick cosmetic of the present invention. Pigments, dyes, fragrances, preservatives, and antioxidants that are usually added to stick cosmetics are added to either the gel or oily component. and,
Glycols such as propylene glycol and 1,3-butylene glycol, which have conventionally been difficult to incorporate because they destroy the gel, can be added, and as a result, contamination by microorganisms can be prevented. As mentioned above, the W/O type emulsion stick cosmetic of the present invention is extremely easy to manufacture, and
It has various advantages such as excellent stability, water retention, bending strength, and spread on the skin, and less contamination by microorganisms. Next, an example will be given and explained. Example 1 State eye cream composition: 1 Liquid paraffin 51.2 (parts by weight) 2 Squalane 10.0 3 Solid paraffin 10.0 4 Candelilla wax 10.0 5 Lanolin 5.0 6 Preservative 0.1 7 Fragrance 0.2 8 Glycerol monooleate 3.0 9 Pyrrolidone carboxylic acid Soda 0.5 10 Purified water 10.0 Manufacturing method: (A) Dissolve 1 to 7. (B) Add solutions 9 and 10 to 8 to form a gel. (C) Add B to A and emulsify. After degassing this, 70
Pour into a molding container at ℃, cool and form into sticks. Example 2 State foundation composition: 1 Liquid paraffin 47.2 (parts by weight) 2 Solid paraffin 10.0 3 Sucrose fatty acid ester 5.0 4 Mixed pigment 15.0 5 Lanolin 5.0 6 Preservative 0.1 7 Fragrance 0.5 8 Diglycerine diisostearate 4.0 9 Sodium citrate 1.0 10 Citric acid 0.2 11 Propylene glycol 2.0 12 Purified water 10.0 Production method: Proceed in the same manner as in Example 1 to obtain a state foundation. Comparative example 1 State eye cream composition: (% by weight) 1 Liquid paraffin 44.7 2 Squalane 10.0 3 Solid paraffin 10.0 4 Candelilla wax 10.0 5 Lanolin 5.0 6 Preservative 0.1 7 Fragrance 0.2 8 Glyceryl monooleate 3.0 9 Sorbitol liquid ( 70% aqueous solution) 10.0 10 Purified water 7.0 Manufacturing method: Follow the same procedure as in Example 1 to obtain a static eye cream. This product is the state eye cream of Example 1 in which sorbitol is added to the gel without adding sodium pyrrolidone carboxylate.
Compared to Example 3, the structure of the stake was weaker and the bending strength was lower. Furthermore, since the emulsifying ability was poor, water retention was poor, light elongation could not be obtained, and the whiteness of the appearance was also reduced. Comparative Example 2 A static eye cream (comparative product 1) was prepared in the same manner as in Example 1, except that sodium pyrrolidone carboxylate was removed from the composition of Example 1, and purified water was added to 10.5 parts by weight. Comparative Example 3 A static foundation (comparative product 2) was prepared in the same manner as in Example 2, except that sodium citrate and citric acid were removed from the composition of Example 2, and purified water was added to 11.2 parts by weight. Test Example 1 The following comparative test was conducted on the eye cream of Example 1 (Invention Product 1) and Comparative Product 1. (1) Stability test based on hardness change <Sample> Product 1 of the present invention and comparative product 1 are filled and molded into a cylindrical container of 14 mmφ x 37 mm. this
Place in a constant temperature bath at 40℃, store for 1 day or 2 weeks, then remove and leave in a constant temperature bath at 20℃ for 2 hours. The sample was taken out from the container and cut into a 14 mmφ x 35 mm cylinder. <Hardness measurement> Measurement was performed using a rheometer NRM-2002J (manufactured by Fudo Kogyo Co., Ltd.) [adapter: piano wire cutter, V-shaped holder] under the conditions of a microwave of 500 g and a table rising speed of 6 cm/min. <Results> Three samples were tested and the results are shown in Table 1.

【表】 第1表から明らかなように、本発明品1は比
較品1にくらべ硬度変化が少なく、安定性に優
れている。 (2) 外観変化 本発明品1及び比較品1を、(1)と同様にして
容器に充填し、40℃の恒温槽に1ケ月保存した
後の外観を観察した。その結果、本発明品1は
調製直後と変化なかつたが、比較品1は透明感
を帯びた外観に変化した。 これから明らかなように、本発明品1は比較
品1にくらべ保存安定性に優れている。 (3) 官能試験 (2)と同様にして40℃で1ケ月保存したもの
(とり出し後20℃に2時間放置後)について、
女子15名による1対比較を行つた。 その結果は第2表のとおりであり、本発明品
1は比較品1にくらべ経時による官能の劣化が
なかつた。
[Table] As is clear from Table 1, Product 1 of the present invention shows less change in hardness than Comparative Product 1, and has excellent stability. (2) Change in Appearance Product 1 of the present invention and Comparative Product 1 were filled into containers in the same manner as in (1), and the appearance was observed after storing them in a constant temperature bath at 40° C. for one month. As a result, the product 1 of the present invention remained unchanged from immediately after preparation, but the appearance of comparative product 1 changed to a transparent appearance. As is clear from this, product 1 of the present invention has better storage stability than comparative product 1. (3) Sensory test For those stored at 40℃ for 1 month in the same manner as in (2) (after being left at 20℃ for 2 hours after removal),
Pairwise comparisons were conducted among 15 women. The results are shown in Table 2, and compared to Comparative Product 1, Product 1 of the present invention showed no deterioration in organoleptic properties over time.

【表】 試験例 2 実施例2のステイツクフアンデーシヨン(本発
明品2)及び比較品2を容器に流し込み充填して
成型し、これを40℃の恒温槽に1ケ月保存後、と
り出して20℃で2時間放置したものについて、女
子15名による1対比較を行つた。その結果は第3
表のとおりであり、本発明品2は比較品2にくら
べて経時による官能の劣化がなかつた。
[Table] Test Example 2 The static foundation of Example 2 (invention product 2) and comparative product 2 were poured into a container, filled and molded, stored in a constant temperature bath at 40°C for one month, and then taken out. A pairwise comparison was conducted by 15 women on the samples that had been left at 20℃ for 2 hours. The result is the third
As shown in the table, the product 2 of the present invention showed no deterioration in organoleptic properties over time compared to the comparative product 2.

【表】【table】

Claims (1)

【特許請求の範囲】 1 HLB9以下の界面活性剤、水及び有機酸又は
その塩類によつて生成されるゲルを油性成分に添
加乳化して得られる油中水型乳化ステイツク化粧
料。 2 界面活性剤が、ソルビタン脂肪酸エステル、
グリセリン脂肪酸エステル、ポリオキシエチレン
硬化ヒマシ油脂肪酸エステル、ジグリセリン脂肪
酸エステル、ポリオキシエチレン硬化ヒマシ油、
ポリオキシエチレンアルキルフエノールの1種又
は2種以上の組合せからなるものである特許請求
の範囲第1項記載の乳化ステイツク化粧料。 3 有機酸がクエン酸、乳酸又はピロリドンカル
ボン酸である特許請求の範囲第1項記載の乳化ス
テイツク化粧料。 4 塩類がアルカリ金属塩である特許請求の範囲
第1項記載の乳化ステイツク化粧料。
[Scope of Claims] 1. A water-in-oil emulsion stick cosmetic obtained by adding and emulsifying a gel produced by a surfactant with an HLB of 9 or less, water, and an organic acid or its salt to an oily component. 2 The surfactant is sorbitan fatty acid ester,
Glycerin fatty acid ester, polyoxyethylene hydrogenated castor oil fatty acid ester, diglycerin fatty acid ester, polyoxyethylene hydrogenated castor oil,
The emulsified stake cosmetic according to claim 1, which comprises one type or a combination of two or more types of polyoxyethylene alkylphenols. 3. The emulsified stake cosmetic according to claim 1, wherein the organic acid is citric acid, lactic acid, or pyrrolidone carboxylic acid. 4. The emulsified stake cosmetic according to claim 1, wherein the salts are alkali metal salts.
JP13018279A 1979-10-09 1979-10-09 Emulsified stick cosmetic Granted JPS5653608A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13018279A JPS5653608A (en) 1979-10-09 1979-10-09 Emulsified stick cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13018279A JPS5653608A (en) 1979-10-09 1979-10-09 Emulsified stick cosmetic

Publications (2)

Publication Number Publication Date
JPS5653608A JPS5653608A (en) 1981-05-13
JPH0133442B2 true JPH0133442B2 (en) 1989-07-13

Family

ID=15028015

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13018279A Granted JPS5653608A (en) 1979-10-09 1979-10-09 Emulsified stick cosmetic

Country Status (1)

Country Link
JP (1) JPS5653608A (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59148713A (en) * 1983-02-10 1984-08-25 Shiseido Co Ltd Pencil-type cosmetic
US6325995B1 (en) * 1992-09-21 2001-12-04 The Procter & Gamble Company Lipsticks compositions containing association structures
JPH0720976U (en) * 1992-11-30 1995-04-18 飯田 萬子 Puff
JP3566739B2 (en) * 1993-09-30 2004-09-15 三省製薬株式会社 Stabilization method for skin external preparation
JP3444329B2 (en) * 1996-04-03 2003-09-08 ポーラ化成工業株式会社 Water-in-oil emulsion composition
JP3444330B2 (en) * 1996-04-03 2003-09-08 ポーラ化成工業株式会社 Water-in-oil emulsion composition
KR20010031712A (en) * 1997-11-14 2001-04-16 후지야마 아키라 Water-in-oil emulsifier compositions
KR20020007062A (en) * 2000-07-15 2002-01-26 손 경 식 Cosmetic composition of water-in-silicone emulsion type
JP2008303164A (en) * 2007-06-06 2008-12-18 Shiseido Co Ltd Water-in-oil type solid makeup cosmetic
JP2010069365A (en) * 2008-09-16 2010-04-02 Dai Ichi Kogyo Seiyaku Co Ltd Method of manufacturing oil-in-water type emulsion composition
JP2011026231A (en) * 2009-07-24 2011-02-10 Rohto Pharmaceutical Co Ltd Stick composition and stick product
WO2019188356A1 (en) * 2018-03-27 2019-10-03 株式会社マンダム Emulsified hairdressing composition

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4965996A (en) * 1972-10-31 1974-06-26
JPS5146588A (en) * 1974-10-19 1976-04-21 Shiseido Co Ltd
JPS53129185A (en) * 1977-04-19 1978-11-10 Shiseido Co Ltd Stable water-in-oil type emulsifier composition

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4965996A (en) * 1972-10-31 1974-06-26
JPS5146588A (en) * 1974-10-19 1976-04-21 Shiseido Co Ltd
JPS53129185A (en) * 1977-04-19 1978-11-10 Shiseido Co Ltd Stable water-in-oil type emulsifier composition

Also Published As

Publication number Publication date
JPS5653608A (en) 1981-05-13

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