JPS61137810A - Cosmetic - Google Patents

Cosmetic

Info

Publication number
JPS61137810A
JPS61137810A JP25974484A JP25974484A JPS61137810A JP S61137810 A JPS61137810 A JP S61137810A JP 25974484 A JP25974484 A JP 25974484A JP 25974484 A JP25974484 A JP 25974484A JP S61137810 A JPS61137810 A JP S61137810A
Authority
JP
Japan
Prior art keywords
fatty acid
acid ester
lower alcohol
polyglycerin fatty
polyglycerin
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.)
Pending
Application number
JP25974484A
Other languages
Japanese (ja)
Inventor
Mitsuo Nonokawa
野々川 光雄
Hidenori Matsuda
松田 秀則
Shunji Yamada
俊二 山田
Michirou Kitahara
路郎 北原
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.)
Nonogawa Shoji Ltd
Original Assignee
Nonogawa Shoji 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 Nonogawa Shoji Ltd filed Critical Nonogawa Shoji Ltd
Priority to JP25974484A priority Critical patent/JPS61137810A/en
Publication of JPS61137810A publication Critical patent/JPS61137810A/en
Pending 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
    • A61K8/18Cosmetics 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
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/26Optical properties
    • A61K2800/262Transparent; Translucent

Abstract

PURPOSE:Cosmetic water-soluble transparently, causing no insoluble substances with time, solubilizing stably an oil-soluble substance such as perfume, etc., having improved water retention effect, using a polyglycerin fatty acid ester which is treated with an aqueous solution of a lower alcohol as a solubilizer for the oil-soluble substance. CONSTITUTION:Cosmetic containing a polyglycerin fatty acid ester which is treated with an aqueous solution of a lower alcohol as a solubilizer for an oil-soluble substance. In a method of treating the polyglycerin fatty acid ester with the aqueous solution of a lower alcohol, the polyglycerin fatty acid ester is dissolved in the aqueous solution of a lower alcohol such as ethanol, etc., the solution is cooled preferably to <=10 deg.C, and a precipitated insoluble substance is purified. The concentration of the fatty acid ester dissolved is preferably <=40wt%. A hydrophilic compound obtained by esterifying 4-18wt% hydroxy group of a polyglycerin (8-16 average polymerization degree) with >=12C higher fatty acid is used as the polyglycerin fatty acid ester.

Description

【発明の詳細な説明】 本発明は低級アルコール水溶液で処理したポリグリセリ
ン脂肪酸エステルを油溶性、物質の可溶化剤として使用
することを特徴とする化粧料に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a cosmetic composition characterized in that a polyglycerol fatty acid ester treated with an aqueous solution of lower alcohol is used as an oil-soluble substance solubilizer.

ポリグリセリン脂肪酸エステルは安全性が高く、食品分
野においてはケーキの起泡剤、コーヒー7レツシユやホ
イップクリーム等の乳化剤、チョコレート製造における
テンパリング工程での粘度低下剤等として広範囲に利用
されている。
Polyglycerin fatty acid esters are highly safe and are widely used in the food field as foaming agents for cakes, emulsifiers for coffee relish and whipped cream, viscosity lowering agents in the tempering process in chocolate manufacturing, etc.

しかし、医薬品や化粧品においての利用は、まだほとん
どなされていない。
However, it has hardly been used in pharmaceuticals or cosmetics yet.

ポリグリセリン脂肪酸エステルは、1分子中に数個の水
酸基を有しており、水酸基の数が多くなるほど高い保水
性を示す。また使用感にも優れていることから、本発明
者等は、保水性を備えた油溶性物質の可溶化剤として、
親水性のポリグリセリン脂肪酸エステルに着目した。し
かし、市販されている親木・性のポリグリセリン脂肪酸
エステルは、水に溶解するが白濁状態でありたり、経時
的に不溶解物を生じたりして使用が困難である。
Polyglycerin fatty acid ester has several hydroxyl groups in one molecule, and the greater the number of hydroxyl groups, the higher the water retention property. In addition, since it has excellent usability, the present inventors used it as a solubilizer for oil-soluble substances with water-retaining properties.
We focused on hydrophilic polyglycerin fatty acid esters. However, commercially available polyglycerin fatty acid esters are difficult to use because they dissolve in water but are cloudy or produce insoluble matter over time.

本発明者等は、これらの問題点を解決すべく鋭意研究し
た結果、低級アルフール水溶液で処理した親水性のポリ
グリセリン脂肪酸エステルは、水に透明に溶解して経時
的に不溶解物を生じず、香料やビタミン類等の油溶性物
質を安定に可溶化できることを見い出した。またポリグ
リセリン脂肪酸エステルの高い保水性により、これを配
合した化粧料は優れた保水効果を持つ。
As a result of intensive research to solve these problems, the present inventors found that hydrophilic polyglycerol fatty acid ester treated with a lower alfur aqueous solution dissolves transparently in water and does not produce insoluble matter over time. It was discovered that oil-soluble substances such as fragrances and vitamins can be stably solubilized. Furthermore, due to the high water retention properties of polyglycerin fatty acid esters, cosmetics containing this have excellent water retention effects.

本発明にいう低級アルコール水溶液でのポリグリセリン
脂肪酸エステルの処理の方法は、エタノール、インプロ
パツール、エチレングリコール、グリセリン、1.3−
ブチレングリコール、プロピレングリコール等の低級ア
ルコールあるいはこれらの混合物の水溶液に、ポリグリ
セリン脂肪酸エステルを溶解する。基本的には、ポリグ
リセリン脂肪酸エステル、低級アルコール及び水をどの
様な順序で溶解してもよく、均一にすればよい。1日以
上放置すると不溶解物が析出し、これを濾過や吸着等に
より除去して透明な溶液とする。ここで不溶解物を完全
に析出させて充分な精製をするためには、10℃以下に
冷却することが好ましい。析出した不溶解物は、ガスク
ロマトグラフィーやケン化価等により、高級脂肪酸のエ
ステル化度の高い親油性のポリグリセリン脂肪酸エステ
ルであると考えられる。
The method of treating polyglycerin fatty acid ester with an aqueous lower alcohol solution according to the present invention includes ethanol, inpropatol, ethylene glycol, glycerin, 1.3-
A polyglycerol fatty acid ester is dissolved in an aqueous solution of a lower alcohol such as butylene glycol, propylene glycol, or a mixture thereof. Basically, polyglycerin fatty acid ester, lower alcohol, and water may be dissolved in any order as long as they are uniform. If left for one day or more, insoluble matter will precipitate, and this will be removed by filtration, adsorption, etc. to form a transparent solution. In order to completely precipitate insoluble matter and perform sufficient purification, it is preferable to cool the mixture to 10° C. or lower. The precipitated insoluble matter is considered to be a lipophilic polyglycerol fatty acid ester with a high degree of esterification of higher fatty acids, as determined by gas chromatography and saponification value.

本発明の低級アルコール水溶液でのポリグリセリン脂肪
酸エステルの処理において、低級アルコール水溶液中の
低級アルフールの濃度ハ、20〜80重景%の範囲で、
好ましくは40〜60重量%である。低級アルコールの
濃度が、20重景%以下あるいは80重量%以上の場合
においては、析出する不溶解物の量が少なく精製が充分
にできないため、本発明においては不適である。
In the treatment of polyglycerol fatty acid ester with a lower alcohol aqueous solution of the present invention, the concentration of lower alfur in the lower alcohol aqueous solution is in the range of 20 to 80%,
Preferably it is 40 to 60% by weight. If the concentration of the lower alcohol is less than 20% by weight or more than 80% by weight, the amount of precipitated insoluble matter will be small and purification will not be sufficient, making it unsuitable for the present invention.

低級アルコール水溶液に溶解するポリグリセリン脂肪酸
エステルの濃度は、40重量%以下が好ましい。ポリグ
リセリン脂肪酸エステルの濃度が40重量%以上になる
と、低級アルコール−水−ポリグリセリン脂肪酸エステ
ルの3成分系の溶液粘度が高くなり、濾過や吸着等によ
る不溶解物の除去が困難となる。
The concentration of polyglycerol fatty acid ester dissolved in the lower alcohol aqueous solution is preferably 40% by weight or less. When the concentration of polyglycerin fatty acid ester is 40% by weight or more, the solution viscosity of the three-component system of lower alcohol-water-polyglycerin fatty acid ester becomes high, making it difficult to remove insoluble matter by filtration, adsorption, etc.

本発明において、低級アルフール水溶液で処理すること
により、油溶性物質の可溶化剤として利用できるポリグ
リセリン脂肪酸エステルは、ポリグリセリン(平均重合
度8〜16)の水酸基の4〜18%を炭素数12以上の
高級脂肪酸でエステル化して得られる化合物で、そのH
LBは約9〜18の範囲にある。HLBf9以下のポリ
グリセリン脂肪酸エステルは、親水性でなくなり、低級
アルコール水溶液の処理では精製することが困難である
。またHLEが、18以上のポリグリセリン脂肪酸エス
テルは、油溶性物質の可溶化力が弱く、本発明において
は不適である。
In the present invention, polyglycerin fatty acid ester, which can be used as a solubilizer for oil-soluble substances by treatment with a lower alfur aqueous solution, is produced by converting 4 to 18% of the hydroxyl groups of polyglycerin (average degree of polymerization 8 to 16) into A compound obtained by esterification with the above higher fatty acids, whose H
LB is in the range of about 9-18. Polyglycerin fatty acid esters with HLBf of 9 or less are no longer hydrophilic and are difficult to purify by treatment with a lower alcohol aqueous solution. Furthermore, polyglycerol fatty acid esters having an HLE of 18 or more have a weak ability to solubilize oil-soluble substances and are therefore unsuitable for the present invention.

本発明に使用されるポリグリセリン脂肪酸エステルの高
級脂肪酸は、炭素数12以上の直鎖又は側鎖の飽和脂肪
酸あるいは不飽和脂肪酸で、例えば、ラウリン酸、ミリ
スチン酸、バルミチン酸、ステアリン酸、ベヘニン酸、
イソパルミチン酸、イソステアリン酸、12−ヒドロキ
システアリン酸、オレイン酸等が載げられる。
The higher fatty acids of the polyglycerin fatty acid ester used in the present invention are linear or side chain saturated or unsaturated fatty acids having 12 or more carbon atoms, such as lauric acid, myristic acid, valmitic acid, stearic acid, and behenic acid. ,
Examples include isopalmitic acid, isostearic acid, 12-hydroxystearic acid, and oleic acid.

次に本発明の方法により精製したポリグリセリンラウレ
ートを用い、単品香料のゲラニオールおよびリナリルア
セテートの可溶化の実験を次に示す処方にて行った。ま
た結果を表1に示す。
Next, using polyglycerol laurate purified by the method of the present invention, an experiment was conducted to solubilize single fragrances geraniol and linalyl acetate using the following formulation. The results are also shown in Table 1.

可溶化実験の処方 プロピレングリフール    5.0重J1%ゲラニオ
ール(又はリナリル 0.2重量%アセテート) 精製水で100重量%にする。
Prescription for solubilization experiment Propylene glyfur 5.0wt J1% geraniol (or linalyl 0.2wt% acetate) Make up to 100% by weight with purified water.

ポリグリセリンラウレートの1(LBが18以上になる
と、単品香料の可溶化力の低下が見られる。また他の脂
肪酸エステルについても同様な結果が得られた。これに
より本発明においては、HLBd;18以上のポリグリ
セリン脂肪酸エステルは不適である。
When the LB of polyglycerol laurate is 18 or more, the solubilizing power of single fragrances decreases. Similar results were also obtained for other fatty acid esters. Therefore, in the present invention, HLBd; Polyglycerin fatty acid esters of 18 or more are unsuitable.

表1 PG;ポリグリセリン ()内の数字;ポリグリセリンの重合度Iにモノラウレ
ート 2L;ジラウレート 次に本発明の実施例を例示して、本発明を具体的に説明
する。尚、実施例中の%は重量%である。
Table 1 PG; Polyglycerin Numbers in parentheses: Degree of polymerization of polyglycerin I, monolaurate 2L; dilaurate Next, the present invention will be specifically explained with reference to Examples. In addition, % in an example is weight %.

![[1,モイスチャーローシッン 香料(グリーンフローラル調)O,OSグリセリン  
          3プロピレングリコール    
   3精製水で100%にする。
! [[1, Moisture rosin fragrance (green floral tone) O, OS glycerin
3 propylene glycol
3 Make it 100% with purified water.

まず50%エタノール水溶液にデカグリセリンモノラウ
レートを均一に溶解する。これを5℃の冷却状態で一日
放置後、析出した不溶解物を濾過すると透明な溶液を得
た。次いでこの溶液に油溶性物質である香料を溶解した
後、順次グリセリン、プロピレングリコール、精製水を
加えると、透明なモイスチャーローションを得た。
First, decaglycerin monolaurate is uniformly dissolved in a 50% ethanol aqueous solution. After this was left in a cooled state at 5° C. for one day, the precipitated insoluble matter was filtered to obtain a transparent solution. Next, after dissolving a fragrance, which is an oil-soluble substance, in this solution, glycerin, propylene glycol, and purified water were sequentially added to obtain a transparent moisturizing lotion.

得られたモイスチャーローシ1ンは、経時的に白濁した
り、不溶解物を生じたりすることはなく安定なものであ
った。また保水性が高く、優れた使用感である。
The obtained moisture lotion was stable without becoming cloudy over time or producing insoluble matter. It also has high water retention and provides an excellent feeling of use.

実施例2. セットローシラン オリーブアルコール       0.2エタノール 
          70ポリビニルピロリドン   
    0.5精製水で100%にする。
Example 2. Set low silane olive alcohol 0.2 ethanol
70 polyvinylpyrrolidone
Make 100% with 0.5 purified water.

実施例1と同様な方法により透明なセットローションを
得た。このセットローシランは保水性が高く、髪がしな
やかに仕上る。
A transparent setting lotion was obtained in the same manner as in Example 1. This setting low silane has high water retention and leaves hair supple.

実施例6. ビタミン入りパラ、り 天然ビタミンE0.1 エタノール            10ポリビニルア
ルコール      13精製水で100%にする。
Example 6. Vitamin-containing para, natural vitamin E0.1 Ethanol 10 Polyvinyl alcohol 13 Make 100% with purified water.

実施例1と同様な方法により透明な被膜式のビタミン入
りバンクを得た。このパックは保水性が高く、使用後し
っとりする。
A transparent film-type vitamin-containing bank was obtained in the same manner as in Example 1. This pack has high water retention and leaves you feeling moisturized after use.

実施例4 ハンドローション 香料(シトラス調)         O,OSエチレ
ングリコール        5尿素        
        2精製水で100%にする。
Example 4 Hand lotion fragrance (citrus tone) O,OS ethylene glycol 5 urea
2 Make it 100% with purified water.

実施例1と同様な方法により透明なハンドローションを
得た。このハンドローン1ンは保水性が高く、ひびや赤
ぎれを防ぐ。
A transparent hand lotion was obtained in the same manner as in Example 1. This hand lawn has high water retention and prevents cracks and redness.

Claims (2)

【特許請求の範囲】[Claims] (1)低級アルコール水溶液で処理したポリグリセリン
脂肪酸エステルを油溶性物質の可溶化剤として使用する
ことを特徴とする化粧料。
(1) A cosmetic product characterized in that a polyglycerin fatty acid ester treated with an aqueous lower alcohol solution is used as a solubilizer for an oil-soluble substance.
(2)ポリグリセリン脂肪酸エステルが、ポリグリセリ
ン(平均重合度8〜16)の水酸基の4〜18%を炭素
数12以上の高級脂肪酸でエステル化して得られる親水
性の化合物あるいはこれらの混合物である、特許請求の
範囲第(1)項記載の化粧料。
(2) The polyglycerin fatty acid ester is a hydrophilic compound obtained by esterifying 4 to 18% of the hydroxyl groups of polyglycerin (average degree of polymerization 8 to 16) with a higher fatty acid having 12 or more carbon atoms, or a mixture thereof. , the cosmetic according to claim (1).
JP25974484A 1984-12-07 1984-12-07 Cosmetic Pending JPS61137810A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25974484A JPS61137810A (en) 1984-12-07 1984-12-07 Cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25974484A JPS61137810A (en) 1984-12-07 1984-12-07 Cosmetic

Publications (1)

Publication Number Publication Date
JPS61137810A true JPS61137810A (en) 1986-06-25

Family

ID=17338343

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25974484A Pending JPS61137810A (en) 1984-12-07 1984-12-07 Cosmetic

Country Status (1)

Country Link
JP (1) JPS61137810A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0267247A (en) * 1988-09-02 1990-03-07 Asahi Denka Kogyo Kk Solubilization of fatty ester sparingly soluble in water

Citations (4)

* 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
JPS5864128A (en) * 1981-10-15 1983-04-16 Matsumoto Seiyaku Kogyo Kk Alcohol-containing aqueous gel composition
JPS5933206A (en) * 1982-08-20 1984-02-23 Shiseido Co Ltd Translucent cosmetic
JPS5987035A (en) * 1982-11-06 1984-05-19 Kawaken Fine Chem Co Ltd W/o type emulsion composition stably containing urea

Patent Citations (4)

* 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
JPS5864128A (en) * 1981-10-15 1983-04-16 Matsumoto Seiyaku Kogyo Kk Alcohol-containing aqueous gel composition
JPS5933206A (en) * 1982-08-20 1984-02-23 Shiseido Co Ltd Translucent cosmetic
JPS5987035A (en) * 1982-11-06 1984-05-19 Kawaken Fine Chem Co Ltd W/o type emulsion composition stably containing urea

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0267247A (en) * 1988-09-02 1990-03-07 Asahi Denka Kogyo Kk Solubilization of fatty ester sparingly soluble in water

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