JPS6025183B2 - Oil-in-polyhydric alcohol emulsion composition - Google Patents

Oil-in-polyhydric alcohol emulsion composition

Info

Publication number
JPS6025183B2
JPS6025183B2 JP54071732A JP7173279A JPS6025183B2 JP S6025183 B2 JPS6025183 B2 JP S6025183B2 JP 54071732 A JP54071732 A JP 54071732A JP 7173279 A JP7173279 A JP 7173279A JP S6025183 B2 JPS6025183 B2 JP S6025183B2
Authority
JP
Japan
Prior art keywords
oil
polyhydric alcohol
fatty acid
emulsion composition
alcohol emulsion
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
JP54071732A
Other languages
Japanese (ja)
Other versions
JPS5655306A (en
Inventor
可丸 熊野
富幸 難波
正昭 石渡
勲 室谷
健一 富田
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 JP54071732A priority Critical patent/JPS6025183B2/en
Publication of JPS5655306A publication Critical patent/JPS5655306A/en
Publication of JPS6025183B2 publication Critical patent/JPS6025183B2/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • A61K8/34Alcohols
    • A61K8/345Alcohols containing more than one hydroxy group
    • 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
    • A61K8/062Oil-in-water emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin

Description

【発明の詳細な説明】 本発明は食品添加物としてその安全性が高いと知られて
いるショ糖脂肪酸ェステルをイ○鉾料及び医薬品に有効
に活用する為、多価アルコール、ショ糖脂肪酸ェステル
及び非イオン界面活性剤とで供してなるゲル状組成物中
に、各種油分を含有せしめて得られる多価アルコール中
瓶型乳化組成物を提供することを目的とするものである
Detailed Description of the Invention The present invention aims to effectively utilize sucrose fatty acid ester, which is known to be highly safe as a food additive, in food additives and pharmaceuticals. The object of the present invention is to provide a polyhydric alcohol medium-bottle emulsion composition obtained by incorporating various oils into a gel-like composition formed by providing a polyhydric alcohol with a nonionic surfactant and a nonionic surfactant.

更に詳しくは、分子内に3個以上の水酸基を有する多価
アルコール1種又は2種以上5〜99%と炭素数8〜2
2の飽和又は不飽和脂肪酸からなるショ糖ェステル置換
度1.腿よ下のショ糖脂肪酸ェステル0.5〜30%及
び3〜18の常温で液状を呈する非イオン界面活性剤0
.1〜20%を加熱混合溶解して得られるゲル状組成物
中に油分を分散内包して得られる多価アルコール中油型
乳化組成物並びに本発明乳化組成物を水に希釈又は水を
加える方法により得られる微粒子の水中油型、クリーム
、乳液、フアウンディション等の化粧料、医薬品、医薬
部外品及び食品を提供できるものである。
More specifically, 5-99% of one or more polyhydric alcohols having three or more hydroxyl groups in the molecule and 8-2 carbon atoms.
Degree of sucrose ester substitution consisting of 2 saturated or unsaturated fatty acids 1. Sucrose fatty acid ester below the thighs 0.5-30% and 3-18% nonionic surfactant that is liquid at room temperature
.. An oil-in-polyhydric alcohol type emulsion composition obtained by dispersing and incorporating an oil component into a gel-like composition obtained by heating and mixing and dissolving 1 to 20% of the composition, and a method of diluting or adding water to the emulsion composition of the present invention. Cosmetics such as oil-in-water type fine particles, creams, emulsions, and foundations, pharmaceuticals, quasi-drugs, and foods can be provided.

本発明の主要物質であるショ糖脂肪酸ェステルは天然の
ショ糖と脂肪酸とで構成された無味無臭の可食性界面活
性物質で、そのすぐれた安全性、生分解性の為、その用
途は食品を中心に極めて広い。特に目や皮膚に対する低
刺激性、薄い脂肪膿生成と適切な水和平衡による皮膚へ
の柔軟性、保護作用は、化粧料や医薬品の基剤開発の用
途として重要である。従釆、かかるショ糖脂肪酸ェステ
ルの特徴に注目し、低刺激性の界面活性剤としてイ8姓
料や医薬品のェマルジョン基剤として古くから検討され
てきているが、従釆の油中水型あるいは水中油型のェマ
ルジョンに単独で主要界面活性剤として使用した際には
、連続相との相漆性、界面張力低下熊などの点から、一
般的にその乳化状態は悪く、最近の化粧料や医薬品のェ
マルジョン基剤に要求される均一な微粒子及び長期安定
性の維持に対しては、なお欠点を有する為、主役の座を
他の界面活性剤にうばわれてきている。
Sucrose fatty acid ester, which is the main substance of the present invention, is a tasteless and odorless edible surfactant composed of natural sucrose and fatty acids. Because of its excellent safety and biodegradability, its use is limited to foods. Extremely spacious in the center. In particular, its low irritation to the eyes and skin, its softness and protective effect on the skin due to thin lipopulence formation and appropriate hydration balance, are important for use in the development of bases for cosmetics and pharmaceuticals. Focusing on the characteristics of such sucrose fatty acid esters, they have been studied for a long time as hypoallergenic surfactants and as emulsion bases for pharmaceuticals. When used alone as the main surfactant in oil-in-water emulsions, the emulsification state is generally poor due to the phase compatibility with the continuous phase and the decrease in interfacial tension. Since it still has drawbacks in maintaining the uniform fine particles and long-term stability required for emulsion bases for pharmaceuticals, other surfactants have taken over the leading role.

本発明者らは、皮膚や目に対して低刺激性であり、且つ
皮膚への柔軟作用、保護作用のすぐれたショ糖脂肪酸ェ
ステルを基剤又は界面活性補助剤として有効に活用した
すぐれたェマルジョン系を得るために、鋭意研究を重ね
た結果、かかるショ糖脂肪酸ェステルを分子内に3個以
上の水酸基を有する多価アルコール1種又は2種以上及
び常温で液状を呈する非イオン界面活性剤とで混合加熱
溶解すると、各成分の相互作用により強固な構造をもつ
ゲル状の均一相を形成する。
The present inventors have developed an excellent emulsion that effectively utilizes sucrose fatty acid ester as a base or surfactant, which is hypoallergenic to the skin and eyes and has excellent softening and protective effects on the skin. In order to obtain this system, as a result of extensive research, we found that the sucrose fatty acid ester was combined with one or more polyhydric alcohols having three or more hydroxyl groups in the molecule and a nonionic surfactant that is liquid at room temperature. When mixed and heated, a gel-like homogeneous phase with a strong structure is formed due to the interaction of each component.

即ち、この均一相の構造は安定な固い液晶相である。こ
こにおけるショ糖脂肪酸ェステルは、分子内に3個以上
の水酸基を有する水溶性多価アルコールとの構造形成機
能(水素結合など)としての役割を果すものである。か
かる3成分の共存による安定な均一相に油分が内包され
る場合、油分は安定に存在し得る。いいかえれば外相に
前記多価アルコール、非イオン界面活性剤、ショ糖脂肪
酸ェステルからなる均一相が後記油分類が分散内包され
る粘稀度の高く、安定な多価アルコール中油型乳化組成
物が得られる。更に、上記方法により得られた本発明物
を他の乳化剤を加えることなしに、水で希釈又は水を加
えて均一混合すると、強力なェネルギ一を加えることな
く、微粒子の均一な水中油型ェマルジョンが得られるこ
とを見し、出し、この知見に基づし・本発明をなすに至
った。本発明において用いられるショ糖脂肪酸ェステル
はェステル置換度1.母〆下のものが全て含有される。
That is, this homogeneous phase structure is a stable, hard liquid crystal phase. The sucrose fatty acid ester here plays a role in forming a structure (such as hydrogen bonding) with a water-soluble polyhydric alcohol having three or more hydroxyl groups in the molecule. When the oil is encapsulated in a stable homogeneous phase due to the coexistence of these three components, the oil can exist stably. In other words, a stable oil-in-polyhydric alcohol emulsion composition with high viscosity in which a homogeneous phase consisting of the polyhydric alcohol, nonionic surfactant, and sucrose fatty acid ester disperses and encapsulates the oil classification described below in the outer phase is obtained. It will be done. Furthermore, if the product of the present invention obtained by the above method is diluted with water or mixed uniformly with water without adding any other emulsifier, a uniform oil-in-water emulsion of fine particles can be obtained without adding strong energy. It was found that this could be obtained, and based on this knowledge, the present invention was made. The sucrose fatty acid ester used in the present invention has an ester substitution degree of 1. Contains everything under the mother's name.

かかる置換度とはショ糖ェステルの構成ショ糖1分子当
りェステル結合した脂肪酸の結合数の平均値を示す。モ
ノェステル含有としては約20〜80%である。又構成
される脂肪酸の炭素数は8〜22の飽和又は不飽和の単
独又は混合脂肪酸である。本発明におけるショ糠脂肪酸
ェステルとしては、置換度1.65以下、モノェステル
含有約40%以上が好ましく、組成比率は0.5〜30
%、好ましくは1〜10%である。
The degree of substitution refers to the average number of ester-bonded fatty acids per molecule of sucrose constituting the sucrose ester. The monoester content is about 20 to 80%. Further, the constituent fatty acids are saturated or unsaturated single or mixed fatty acids having carbon numbers of 8 to 22. The bran fatty acid ester in the present invention preferably has a degree of substitution of 1.65 or less, a monoester content of about 40% or more, and a composition ratio of 0.5 to 30%.
%, preferably 1 to 10%.

0.5%以下では多価アルコールとショ糖脂肪酸ヱステ
ルとの一次ゲル組成物は作りにくく、又、30%以上で
は完全分散不可能である。
If it is less than 0.5%, it is difficult to form a primary gel composition of polyhydric alcohol and sucrose fatty acid ester, and if it is more than 30%, complete dispersion is impossible.

本発明における多価アルコールは、分子内に3個以上の
水酸基を有する水溶性の多価アルコールで、グリセリン
、ジグリセリン、トリグリセリン、テトラグリセリン、
ベンタグリセリン、ヘキサグリセリン、オクタグリセリ
ン、ノナグリセリン、デカグリセリン、グルコース、ソ
ルビト−ル、マルチトール、シユークローズ、ラフイノ
ース、トレハロースなどであり、1種又は2種以上の混
合物である。
The polyhydric alcohol in the present invention is a water-soluble polyhydric alcohol having three or more hydroxyl groups in the molecule, such as glycerin, diglycerin, triglycerin, tetraglycerin,
These include bentaglycerin, hexaglycerin, octaglycerin, nonaglycerin, decaglycerin, glucose, sorbitol, maltitol, seurose, raffinose, trehalose, etc., and they are one type or a mixture of two or more types.

特に好ましいのはグリセリン、ジグリセリン、トリグリ
セリン、ソルビトール、マルチトールの1種または2種
の混合物である。上記多価アルコールの組成比率は、得
られる乳化組成物の使用感触、安全性、粘鋼性などによ
り変化するが5〜99%、好ましくは15〜99%であ
る。5%以下ではゲル破壊が起り乳化組成物は不可能で
ある。
Particularly preferred are one or a mixture of two of glycerin, diglycerin, triglycerin, sorbitol, and maltitol. The composition ratio of the polyhydric alcohol varies depending on the feeling of use, safety, viscosity, etc. of the resulting emulsified composition, but is 5 to 99%, preferably 15 to 99%. If it is less than 5%, gel destruction occurs and an emulsified composition cannot be prepared.

水酸基が1個ないし2個のアルコール中では、即ち、メ
タノール、エタノール、エチレングリコール、プロピレ
ングリコール、1,3ープチレングリコール、ジプロピ
レングリコールなど中では、本発明の根幹となるショ糖
脂肪酸ェステルによる構造形成が不可能であるため、本
発明の如き、多価アルコール中油型乳化組成物を得るこ
とはできない。本発明における非イオン界面活性剤は、
常温で液状を呈することが必要である。
In alcohols having one or two hydroxyl groups, that is, methanol, ethanol, ethylene glycol, propylene glycol, 1,3-butylene glycol, dipropylene glycol, etc., sucrose fatty acid ester, which is the basis of the present invention, is used. Since structure formation is not possible, it is not possible to obtain an oil-in-polyhydric alcohol emulsion composition as in the present invention. The nonionic surfactant in the present invention is
It is necessary to exhibit a liquid state at room temperature.

これらの非イオン界面活性剤はHLB3〜18で高級ア
ルコールポリオキシェチレンェーテル化合物、高級脂肪
酸ポリオキシェチレンェステル化合物、ポリオキシェチ
レングリセリン脂肪酸ェステル、ポリオキシェチレンソ
ルビタン脂肪酸ェステル、ポリオキシェチレンソルビト
ール脂肪酸ェステル、グリセリンヒドロキシ脂肪酸ェス
テルポリオキシェチレン付加物、ソルビタン脂肪酸ェス
テルポリオキシェチレン付加物、ソルビトール脂肪酸ェ
ステルポリオキシェチレン付加物、グリセリン脂肪酸ェ
ステル、ソルビタン脂肪酸ェステル、ソルビトール脂肪
酸ェステル、トリメチロールェタン脂肪酸ェステル、ト
リメチロールプロパン脂肪酸ェステル、ベンタェリスリ
トール脂肪酸ェステル、高級アルコール及び高級アルコ
ールエチレンオキシド付加物のリン酸ェステル、高級脂
肪酸モノ(ジ)ェタ/ールアマィドなどである。これら
のうち特に好ましいのは、グリセリンモノイソステアレ
ート、ジグリセリンジイソステアレート、グリセリンモ
ノオレート、ジグリセリンジオレート、グリセリンジリ
シノレート、ソルビタンモノ(セスキ、ジ、トリ)オレ
ート、ソルビタンモノラウリン酸ェステルェチレンオキ
シド付加物、ソルビタンモノオレィン酸ェステルヱチレ
ンオキシド付加物、グリセリンヒドロキシステアリン酸
ェステルェチレンオキシド付加物、オレィレアルコール
ポリオキシェチレンェーテル付加物などである。以上記
載したうちの常温で液状である非イオン界面活性剤の機
能は、本発明乳化組成物中に加わる各種油分の乳化剤と
して作用すると同時に、ショ糖脂肪酸ェステル及び水溶
性多価アルコールとの共存において構成される構造形成
促進剤としての役割も果すものである。
These nonionic surfactants have an HLB of 3 to 18, and contain higher alcohol polyoxyethylene ether compounds, higher fatty acid polyoxyethylene ester compounds, polyoxyethylene glycerin fatty acid esters, polyoxyethylene sorbitan fatty acid esters, and polyoxyethylene sorbitan fatty acid esters. Oxyethylene sorbitol fatty acid ester, glycerin hydroxy fatty acid ester polyoxyethylene adduct, sorbitan fatty acid ester polyoxyethylene adduct, sorbitol fatty acid ester polyoxyethylene adduct, glycerin fatty acid ester, sorbitan fatty acid ester, sorbitol These include fatty acid esters, trimethylolethane fatty acid esters, trimethylolpropane fatty acid esters, bentaerythritol fatty acid esters, phosphate esters of higher alcohols and higher alcohol ethylene oxide adducts, and higher fatty acid mono(di)eta/ruamides. Among these, particularly preferred are glycerin monoisostearate, diglycerin diisostearate, glycerin monooleate, diglycerin diolate, glycerin diricinolate, sorbitan mono(sesqui, di, tri) oleate, sorbitan monolaurate, etc. These include stellethylene oxide adduct, sorbitan monooleic acid ester ethylene oxide adduct, glycerol hydroxystearic acid ester ethylene oxide adduct, oleylalcohol polyoxyethylene ether adduct, and the like. The function of the nonionic surfactant described above, which is liquid at room temperature, is to act as an emulsifier for various oils added to the emulsified composition of the present invention, and at the same time, to coexist with the sucrose fatty acid ester and the water-soluble polyhydric alcohol. It also plays a role as a structure formation promoter.

かかる目的の為、非イオン界面活性剤の形態が常温固体
である場合には、構造形成促進剤として作用する前に、
非イオン界面活性剤自身が凝固によりゲル状細成物を破
壊し、油を解油するため本発明乳化組成物の形成はでき
ない。
For this purpose, when the nonionic surfactant is solid at room temperature, before it acts as a structure formation promoter,
The emulsified composition of the present invention cannot be formed because the nonionic surfactant itself destroys the gel-like fine product through coagulation and dissolves the oil.

しかし使用する非イオン界面活性剤が液体である場合に
は、全くこの限りでなく低温(000)においても安定
な多価アルコール中油型乳化組成物が得られる。非イオ
ン界面活性剤の組成比率は0.1〜20%、好ましくは
0.5〜10%である。0.1%以下では不透明固化し
、本発明目的の多価アルコール中油型乳化組成物は得ら
れない。
However, when the nonionic surfactant used is a liquid, this is not the case at all, and an oil-in-polyhydric alcohol emulsion composition that is stable even at low temperatures (000) can be obtained. The composition ratio of the nonionic surfactant is 0.1 to 20%, preferably 0.5 to 10%. If it is less than 0.1%, it becomes opaque and solidified, and the oil-in-polyhydric alcohol emulsion composition intended for the present invention cannot be obtained.

又、20%以上では構造形成がとれなくなる為、粘性が
著しく低下し、実用的ではない。本発明における油分は
、化粧料及び、医薬品、食品等に通常用いられる動植物
系油脂、炭化水素化合物、香料などのいずれでもよく、
それぞれの構成比率は系の外観、使用性、安定性などの
目的により任意選択される。本発明乳化組成物の硬度は
実施例1〜5で述べるが、内相比や非イオン界面活性剤
の配合量に依存し、内相比が増大するにつれて堅くなる
為、求められる粘鋼性、使用性により適宜選択し得る。
Moreover, if it is more than 20%, the structure cannot be formed and the viscosity decreases significantly, which is not practical. The oil in the present invention may be any animal or vegetable oil, hydrocarbon compound, fragrance, etc. commonly used in cosmetics, medicines, foods, etc.
The respective composition ratios are arbitrarily selected depending on the objectives such as the appearance, usability, and stability of the system. The hardness of the emulsified composition of the present invention will be described in Examples 1 to 5, but it depends on the internal phase ratio and the amount of nonionic surfactant, and as the internal phase ratio increases, it becomes harder. It can be selected as appropriate depending on the usability.

又、後述の実施例6〜13で述べるが、本発明乳化組成
物の生成に対しては、油分の極性にはほとんど影響を受
けない。次に実施例より本発明をさらに詳細に説明する
Furthermore, as described in Examples 6 to 13 below, the production of the emulsified composition of the present invention is hardly affected by the polarity of the oil component. Next, the present invention will be explained in more detail with reference to Examples.

(実施例1〜5) ただし、内相比は■/■十■十■+■で表わす。(Examples 1 to 5) However, the internal phase ratio is expressed as ■/■10■10■+■.

表中■〜■を70℃に加熱溶解混合し、第一次ゲル状組
成物を作る。
In the table, ① to ② were heated and mixed at 70°C to prepare a primary gel composition.

これにあらかじめ70℃に加熱した■を徐々にラボミキ
サーで縄梓混合する。これを30qoまで鷹梓冷却して
本発明多価アルコール中油型乳化組成物を得る。(実施
例 6〜13) 内相比0.65に統一した透明多価アルコール中油型乳
化組成物なお、表中A,B,C,Dは比較例を示す。
This was gradually mixed with (2) heated to 70°C in advance using a lab mixer. This is cooled down to 30 qo to obtain an oil-in-polyhydric alcohol emulsion composition of the present invention. (Examples 6 to 13) Transparent oil-in-polyhydric alcohol emulsion compositions having an internal phase ratio of 0.65. In the table, A, B, C, and D indicate comparative examples.

実施例1〜5と同様な方法で作成した。比較例A〜Dは
本発明以外のものを示し、比較例A及びCはゲルは生成
するが白色を呈し、水添加により得られたェマルジョン
は不安定である。比較例B,Cではゲル状組成物は全く
できない。(実施例 14〜17)内相比0.725に
統一した透明多価アルコール中油型乳化組成物実施例1
と同様な方法で作成した。
It was created in the same manner as Examples 1-5. Comparative Examples A to D show products other than those of the present invention, and in Comparative Examples A and C, a gel is formed, but it is white in color, and the emulsion obtained by adding water is unstable. In Comparative Examples B and C, gel-like compositions were not formed at all. (Examples 14 to 17) Transparent oil-in-polyhydric alcohol emulsion composition Example 1 with a unified internal phase ratio of 0.725
created in a similar manner.

(実施例 18) 透明軟こう 佃を70qoに加熱混合溶解した中に、あらかじめ70
ooに溶解した凶を徐々に麓拝混合したものを、30o
oまで冷却すると透明軟こうを得る。
(Example 18) In advance, 70 qo of transparent soft rice cake was heated and mixed and dissolved to 70 qo.
The mixture of evil dissolved in oo is gradually added to 30o.
Upon cooling to o, a transparent ointment is obtained.

次ぎに、本発明の多価アルコール中油型乳化組成物を水
に希釈又は水を加える方法で得られる化粧料の例を示す
。参考例 1 透明軟こう状フェィシャルリンス剤 実施例18の本発明乳化組成物を少量手にとり、適当量
の水で希釈してフェィシャルリンス剤とする。
Next, examples of cosmetics obtained by diluting or adding water to the oil-in-polyhydric alcohol emulsion composition of the present invention will be shown. Reference Example 1 Transparent ointment-like facial rinse A small amount of the emulsified composition of the present invention of Example 18 is taken into hand and diluted with an appropriate amount of water to prepare a facial rinse.

参考例 2 乳液 「スクワラン ー肌T% 【B}を7ぴ0に加熱混合溶解した中に、あらかじめ7
0℃に溶解した凶を徐々に加えた本発明乳化組成物を得
る。
Reference Example 2 Milky lotion "Squalane - Skin T% [B]" was mixed and dissolved by heating to 7.
An emulsified composition of the present invention is obtained by gradually adding the soybean paste dissolved at 0°C.

Claims (1)

【特許請求の範囲】 1 分子内に3個以上の水酸基を有する多価アルコール
とエステル置換度1.8以下のシヨ糖脂肪酸エステル及
び常温で液状を呈する非イオン界面活性剤を加熱混合し
て得られるゲル状組成物に油分を加えてなる多価アルコ
ール中油型乳化組成物。 2 多価アルコールがグリセリン、ジグリセリン、ポリ
グリセリン、トリメチロールエタン、トリメチロールプ
ロパン、エリスリトール、ペンタエリスリトール、ソル
ビタン、グルコース、ソルビトール、マルチトール、シ
ユークローズ、ラフイノース、トレハロースの1種又は
2種以上で、その組成比率が5〜99%である特許請求
の範囲第1項記載の多価アルコール中油型乳化組成物。 3 エステル置換度1.8以下のシヨ糖脂肪酸エステル
が炭素数8〜22の飽和脂肪酸からなる化合物で、その
組成比率が0.5〜30%である特許請求の範囲第1項
記載の多価アルコール中油型乳化組成物。4 非イオン
界面活性剤がHLB値3〜18の常温で液状を呈する化
合物で、その組成比率が0.1〜20%である特許請求
の範囲第1項記載の多価アルコール中油型乳化組成物。 5 油分が常温固体から液状までの炭化水素化合物、高
級アルコール高級脂肪酸モノエステル化合物、2塩基酸
高級アルコールジエステル化合物、グリコール高級脂肪
酸ジエステル化合物、動植物油又は合成トリグリセライ
ド化合物の1種又は2種以上である特許請求の範囲第1
項記載の多価アルコール中油型乳化組成物。 6 化粧料である特許請求の範囲第1項記載の多価アル
コール中油型乳化組成物。
[Claims] 1. A polyhydric alcohol having three or more hydroxyl groups in the molecule, a sucrose fatty acid ester with a degree of ester substitution of 1.8 or less, and a nonionic surfactant that is liquid at room temperature. An oil-in-polyhydric alcohol emulsion composition obtained by adding an oil to a gel-like composition. 2. The polyhydric alcohol is one or more of glycerin, diglycerin, polyglycerin, trimethylolethane, trimethylolpropane, erythritol, pentaerythritol, sorbitan, glucose, sorbitol, maltitol, xyucrose, raffinose, and trehalose. The oil-in-polyhydric alcohol emulsion composition according to claim 1, wherein the composition ratio is 5 to 99%. 3. The polyhydric compound according to claim 1, wherein the sucrose fatty acid ester having a degree of ester substitution of 1.8 or less is a compound consisting of a saturated fatty acid having 8 to 22 carbon atoms, and the composition ratio thereof is 0.5 to 30%. Oil-in-alcohol emulsion composition. 4. The oil-in-polyhydric alcohol emulsion composition according to claim 1, wherein the nonionic surfactant is a compound exhibiting a liquid state at room temperature with an HLB value of 3 to 18, and the composition ratio thereof is 0.1 to 20%. . 5 The oil content is one or more of hydrocarbon compounds ranging from solid to liquid at room temperature, higher alcohol higher fatty acid monoester compounds, dibasic acid higher alcohol diester compounds, glycol higher fatty acid diester compounds, animal and vegetable oils, or synthetic triglyceride compounds. Claim 1
The oil-in-polyhydric alcohol emulsion composition described in 1. 6. The oil-in-polyhydric alcohol emulsion composition according to claim 1, which is a cosmetic.
JP54071732A 1979-06-07 1979-06-07 Oil-in-polyhydric alcohol emulsion composition Expired JPS6025183B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP54071732A JPS6025183B2 (en) 1979-06-07 1979-06-07 Oil-in-polyhydric alcohol emulsion composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP54071732A JPS6025183B2 (en) 1979-06-07 1979-06-07 Oil-in-polyhydric alcohol emulsion composition

Publications (2)

Publication Number Publication Date
JPS5655306A JPS5655306A (en) 1981-05-15
JPS6025183B2 true JPS6025183B2 (en) 1985-06-17

Family

ID=13468981

Family Applications (1)

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

Country Link
JP (1) JPS6025183B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0348273U (en) * 1989-09-18 1991-05-08

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5637040A (en) * 1979-08-31 1981-04-10 Nippon Saafuakutanto Kogyo Kk Oil-in-polyhydric alcohol type emulsifying composition
FR2523134A1 (en) * 1982-03-11 1983-09-16 Rhone Poulenc Spec Chim Liq. compsn. contg. mucro:glyceride and edible oil - useful as emulsifier for food and cosmetic prods.
FR2541286A2 (en) * 1983-02-21 1984-08-24 Rhone Poulenc Spec Chim New preparation of sucroglycerides in free-flowing form, process for producing it and its applications
JPS60125244A (en) * 1983-12-13 1985-07-04 Lion Corp Preparation of stable oil-in-water type emulsion
JPH0693996B2 (en) * 1984-12-03 1994-11-24 武田薬品工業株式会社 Emulsified composition
JPS61260011A (en) * 1985-05-14 1986-11-18 Nonogawa Shoji:Kk Thickening, gelatinizing agent composition for oil, using cationic surface active agent
JPS61259751A (en) * 1985-05-14 1986-11-18 Nonogawa Shoji:Kk Preparation of emulsion
CA1295553C (en) * 1986-12-12 1992-02-11 Mohan Vishnupad Water rinsable petroleum jelly water-in-oil emulsion
JPH0816047B2 (en) * 1987-08-17 1996-02-21 株式会社資生堂 Translucent liquid cosmetics
JP2711541B2 (en) * 1987-12-28 1998-02-10 有限会社野々川商事 Polyhydric alcohol-in-oil emulsion composition and oil-in-water emulsion composition
JP3187622B2 (en) 1993-10-07 2001-07-11 カネボウ株式会社 Liposome
JP2001206817A (en) * 1999-11-15 2001-07-31 Shiseido Co Ltd Oil-in-polyhydric alcohol type thermal substrate
KR100633022B1 (en) * 1999-11-15 2006-10-11 가부시키가이샤 시세이도 Oil-in-polyhydric alcohol thermal base
AU2003288987A1 (en) * 2002-11-27 2004-06-18 Minophagen Pharmaceutical Co., Ltd. Oil/glycyrrhizin-containing surfactant phase type gel composition
JP2009126791A (en) * 2007-11-20 2009-06-11 Kracie Home Products Kk Oil-in-polyhydric alcohol type emulsified cosmetic

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5538333A (en) * 1978-09-11 1980-03-17 Kanebo Ltd Improved creamy skin cosmetic

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5538333A (en) * 1978-09-11 1980-03-17 Kanebo Ltd Improved creamy skin cosmetic

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0348273U (en) * 1989-09-18 1991-05-08

Also Published As

Publication number Publication date
JPS5655306A (en) 1981-05-15

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