JPH06227939A - Cosmetic - Google Patents

Cosmetic

Info

Publication number
JPH06227939A
JPH06227939A JP5042089A JP4208993A JPH06227939A JP H06227939 A JPH06227939 A JP H06227939A JP 5042089 A JP5042089 A JP 5042089A JP 4208993 A JP4208993 A JP 4208993A JP H06227939 A JPH06227939 A JP H06227939A
Authority
JP
Japan
Prior art keywords
acid
oil
expressed
formula
skin
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
JP5042089A
Other languages
Japanese (ja)
Inventor
Fumio Deguchi
二三男 出口
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.)
Yuka Sangyo Co Ltd
Original Assignee
Yuka Sangyo 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 Yuka Sangyo Co Ltd filed Critical Yuka Sangyo Co Ltd
Priority to JP5042089A priority Critical patent/JPH06227939A/en
Publication of JPH06227939A publication Critical patent/JPH06227939A/en
Pending legal-status Critical Current

Links

Landscapes

  • Cosmetics (AREA)

Abstract

PURPOSE:To obtain a cosmetic using a vegetable oil, excellent in affinity, emollient and water holding properties, softening permeability and dispersibility and having high safety. CONSTITUTION:This cosmetic comprises lesquerella oil contained in an amount of 25-26% in a seed of a herb belonging to the genus Lesquerella and/or its hydrogenated substance. The lequerella oil has the composition of about 56% lesquerolic expressed by formula I, 14-17% oleic acid (containing isomers), 7-9% linoleic acid, 9-11% linolenic acid, 3-4% auricolic acid expressed by formula II, densipolic acid expressed by formula III and a small amount of fatty acids and the fatty acid, expressed by formula I and accounting for a half or more thereof is capable of manifesting characteristics of no stickiness at all in spite of its affinity for the skin, excellent in emollient properties derived from hydroxyl group and far better moistness imparted to the skin than that of other vegetable oils. Furthermore, the special fatty acids (formulas II and III) contained in a small amount have characteristics improved in softening permeability for the skin due to their excellence in water holding properties.

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、化粧料、さらに詳しく
は、レスクレラ油またはその水素添加物を配合した化粧
料に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to cosmetics, and more particularly to cosmetics containing rescrelar oil or a hydrogenated product thereof.

【0002】[0002]

【従来の技術】従来より、オリーブ油、椿油、ひまし
油、マカデミアナッツ油、メドフォーム油など多くの植
物油が化粧品に使用されいる。
2. Description of the Related Art Conventionally, many vegetable oils such as olive oil, camellia oil, castor oil, macadamia nut oil and medfoam oil have been used in cosmetics.

【0003】また、レスクレラは、米国アリゾナ州やテ
キサス州に野生している植物で、最近になって栽培が研
究され始めたばかりである。
Resclera is a plant that is wild in Arizona and Texas in the United States, and its cultivation has just recently been studied.

【0004】[0004]

【発明が解決しようとする課題】しかし、従来の植物油
を用いた化粧料は、皮膚への親和性とべとつきがない性
質を同時に求めることができず、また、エモリエント
性、抱水性、柔軟浸透性の向上や、充填剤の分散性に優
れたものとするため各種添加剤を加える必要があり、さ
らに、皮膚に対する感触や、安定性、安全性の面からも
様々な問題があった。
However, conventional cosmetics using vegetable oils cannot simultaneously have affinity for skin and non-greasy properties, and also have emollient, water-holding and soft penetrating properties. It is necessary to add various additives in order to improve the heat resistance and the dispersibility of the filler, and further, there are various problems in terms of touch to the skin, stability, and safety.

【0005】本発明は、親和性、エモリエント性、抱水
性、柔軟浸透性、分散性に優れ、かつ安全性の高い植物
油を用いた化粧料を提供することを目的とする。
An object of the present invention is to provide a cosmetic using a vegetable oil which is excellent in affinity, emollient property, water-holding property, soft penetrating property, dispersibility and is highly safe.

【0006】[0006]

【課題を解決するための手段】そこで、本発明者は、上
記課題を解決するため鋭意研究を重ねた結果、親和性、
べとつき、エモリエント性、しっとり感は、脂肪酸構成
と水酸基の位置に関係があり、レスクレラ油(Lesquerel
la Oil)の脂肪酸構成が前記課題を解決することができ
るとの知見を得て本発明を完成した。
The inventors of the present invention have conducted extensive studies to solve the above problems, and as a result,
Stickiness, emollientity, and moistness are related to the composition of fatty acids and the positions of hydroxyl groups.
The present invention has been completed based on the finding that the fatty acid composition of (la oil) can solve the above problems.

【0007】すなわち、本発明の構成は、レスクレラ油
及び/またはその水素添加物を含有してなる化粧料であ
る。
[0007] That is, the constitution of the present invention is a cosmetic containing resclere oil and / or its hydrogenated product.

【0008】レスクレラは10月から11月に植えつ
け、5月から6月にかけて収穫されるが、その種子は約
25%ないし26%の油分を含有する。このレスクレラ
油を構成する脂肪酸組成の一例を示すと次の通りであ
る。 レスクロリック酸(Lesquerolic acid) 約56% オレイン酸(異性体を含む) 14〜17% リノール酸 7〜 9% リノレイン酸 9〜11% オーリコリック酸(Auricolic acid) 3〜 4% デンシポリック酸(Densipolic acid) 少量
Resclera is planted from October to November and harvested from May to June, the seeds of which contain about 25% to 26% oil. An example of the fatty acid composition that constitutes this resclere oil is as follows. Resquerolic acid 56% oleic acid (including isomers) 14-17% Linoleic acid 7-9% Linoleic acid 9-11% Auricolic acid 3-4% Densipolic acid acid) small amount

【0009】レスクロリック酸は、化1に示すように、
炭素数20のモノエン酸で14位置に水酸基を有する特
殊脂肪酸である。また、オーリコリック酸は、化2に示
すように、炭素数20のジエン酸でやはり14位置に水
酸基を有し、デンシポリック酸は、化3のように、炭素
数18のモノエン酸で12位置に水酸基を有する脂肪酸
である。さらにレスクレラ油には、オレイン酸の異性体
も含有するなど、その脂肪酸構成から見ても従来にない
特性を有する植物油である。
Reschloric acid, as shown in Chemical formula 1,
It is a special fatty acid which is a monoenoic acid having 20 carbon atoms and has a hydroxyl group at the 14th position. Further, as shown in Chemical formula 2, auricholic acid is a dienoic acid having 20 carbon atoms and also has a hydroxyl group at the 14-position, and densipolic acid is a monoenoic acid having 18 carbon atoms at the 12-position as shown in Chemical formula 3. It is a fatty acid having a hydroxyl group. Furthermore, rescrelar oil is a vegetable oil having unprecedented properties in terms of its fatty acid composition, such as containing isomers of oleic acid.

【化1】 [Chemical 1]

【化2】 [Chemical 2]

【化3】 [Chemical 3]

【0010】また、レスクレラ油の分析値の一例は次の
通りである。 酸価 0.3 鹸化価 173.8 沃素価 106.4 水酸基価 97.7
Further, an example of the analytical value of rescrelar oil is as follows. Acid value 0.3 Saponification value 173.8 Iodine value 106.4 Hydroxyl value 97.7

【0011】本発明者らは、このレスクレラ油の化粧品
への応用について検討し、従来の植物油にはない特性を
有することを見いだした。
The present inventors have examined the application of this rescrelar oil to cosmetics and found that it has properties that conventional vegetable oils do not have.

【0012】すなわち、レスクレラ油の半分以上を構成
するレスクロリック酸が炭素数20の水酸基含有脂肪酸
で、しかもその水酸基が炭素鎖のほぼ中央に位置するこ
とから、皮膚に親和性有しながらべとつきがまったくな
いという特性を発揮する。また水酸基に由来するエモリ
エント性も優れ皮膚に与えるしっとり感は他の植物油よ
りはるかに優っている。さらに少量含まれている特殊脂
肪酸は抱水性がよいため皮膚に対する柔軟浸透性に優れ
た特性を有する。
That is, since the reschloric acid that constitutes more than half of the rescrelar oil is a fatty acid containing a hydroxyl group having 20 carbon atoms, and the hydroxyl group is located in the approximate center of the carbon chain, it is sticky while having an affinity for the skin. Demonstrate the characteristic that there is no. In addition, the emollient property derived from the hydroxyl group is excellent, and the moist feeling given to the skin is far superior to other vegetable oils. Further, the special fatty acid contained in a small amount has a good water-holding property and thus has a property of excellent softness and penetrability to the skin.

【0013】また、水素添加したレスクレラ油はワック
ス状であり、スティック状製品への応用が出来るが、こ
の場合も充填剤の分散性に優れているため、使用感が非
常に滑らかであるという特性を発揮する。さらに、レス
クレラ油は、非常にマイルドで毒性がなく、このことは
油かす中に毒性物質が無い飼料用植物油としてレスクレ
ラ油が注目されてきたことからも理解し得ることができ
る。
Further, the hydrogenated rescler oil has a waxy form and can be applied to stick-shaped products, but in this case as well, the dispersibility of the filler is excellent, so that the feeling of use is very smooth. Exert. Furthermore, resclere oil is very mild and non-toxic, which can be understood from the fact that rescler oil has been attracting attention as a feed-use vegetable oil that has no toxic substances in the dregs.

【0014】[0014]

【実施例】次に本発明の実施例をあげて説明する。 実施例1(O/W型乳液) (A)油相 レスクレラ油 10.00 ステアリン酸 2.00 グリセリルモノステアレート 3.00 プロピルパラベン 0.05 イソプロピルミリステート 2.00 セタノール 2.00 (B)水相 精製水 74.40 ビーガムR 1.50 トリエタノールアミン 1.00 グリセリン 4.00 メチルパラベン 0.05 (C)香料 適量EXAMPLES Next, examples of the present invention will be described. Example 1 (O / W type emulsion) (A) Oil phase Resclera oil 10.00 Stearic acid 2.00 Glyceryl monostearate 3.00 Propylparaben 0.05 Isopropyl myristate 2.00 Cetanol 2.00 (B) Aqueous phase Purified water 74.40 Veegum R 1.50 Triethanolamine 1.00 Glycerin 4.00 Methylparaben 0.05 (C) Fragrance Suitable amount

【0015】ビーガムを徐々に水に添加し、均質になる
まで攪拌し75℃に加熱し、残りの水相成分(B)を攪
拌しながら加える。次いで78℃まで加熱した油相成分
(A)を水相成分(B)に混合し、50℃まで冷却した
後、香料(C)を添加し、攪拌を続けながら30℃まで
冷却して乳液を得た。得られた乳液は、さらっとした感
じを与えべとつきがまったくなかった。
[0015] Veegum is gradually added to water, stirred until homogeneous and heated to 75 ° C, and the remaining aqueous phase component (B) is added with stirring. Next, the oil phase component (A) heated to 78 ° C. is mixed with the aqueous phase component (B), and after cooling to 50 ° C., the fragrance (C) is added, and the mixture is cooled to 30 ° C. while continuing stirring to obtain an emulsion Obtained. The resulting emulsion gave a dry feel and was completely non-greasy.

【0016】実施例2(W/O型クリーム) (A)油相 流動パラフィン 23.60 蜜ロウ 16.00 水素添加ラノリン 3.00 レスクレラ油 22.00 プロピレングリコールモノステアレート 6.00 セレシン 5.00 プロピルパラベン 0.10 (B)水相 精製水 23.00 ほう砂 1.30 (C)香料 適量Example 2 (W / O type cream) (A) Oil phase Liquid paraffin 23.60 Beeswax 16.00 Hydrogenated lanolin 3.00 Resclera oil 22.00 Propylene glycol monostearate 6.00 Ceresin 5. 00 Propylparaben 0.10 (B) Water phase Purified water 23.00 Borax 1.30 (C) Perfume Suitable amount

【0017】油相(A)を85℃まで加熱し、これとは
別に水相(B)も85℃まで加熱する。水相を油相へ混
合し、十分に攪拌し35℃まで冷却した後、コロイドミ
ルまたはホモジナイザーを用いてより均質で安定なエマ
ルジョンを得た。得られた乳液は、皮膚への親和性が強
くしっとり感を与えた。
The oil phase (A) is heated to 85 ° C., and the water phase (B) is also heated to 85 ° C. separately. The aqueous phase was mixed with the oil phase, thoroughly stirred and cooled to 35 ° C., and then a more homogeneous and stable emulsion was obtained using a colloid mill or a homogenizer. The obtained emulsion had a strong affinity for the skin and gave a moist feeling.

【0018】実施例3(ハンドクリーム) (A)油相 グリセリルモノステアレート 4.30 ステアリン酸 6.80 イソプロピルミリステート 4.10 PEG(1500)モノイソステアレート 5.70 レスクレラ油 5.00 ラノリン 1.00 (B)水相 プロピレングリコール 2.40 精製水 70.60 メチルパラベン 0.10Example 3 (Hand cream) (A) Oil phase Glyceryl monostearate 4.30 Stearic acid 6.80 Isopropyl myristate 4.10 PEG (1500) monoisostearate 5.70 Resclera oil 5.00 Lanolin 1.00 (B) Aqueous phase Propylene glycol 2.40 Purified water 70.60 Methylparaben 0.10

【0019】油相(A)、水相(B)を別々に70℃に
加熱し、ついで、水相を油相に加えゆっくり攪拌しなが
ら冷却し、ハンドクリームを得た。得られたハンドクリ
ームは、のびが優れており柔軟性を皮膚に与えた。
The oil phase (A) and the aqueous phase (B) were separately heated to 70 ° C., and then the aqueous phase was added to the oil phase and cooled with slow stirring to obtain a hand cream. The obtained hand cream was excellent in spreadability and imparted flexibility to the skin.

【0020】実施例4(ヘアドレッシングクリーム) (A)油相 液状ラノリン 3.00 イソプロピルパルミテート 15.00 ビーズワックス 3.00 ソルビタンモノオレエート 2.00 レスクレラ油 25.00 水素添加レスクレラ油 5.00 ワセリン 6.00 プロピルパラベン 0.03 (B)水相 グリセリン 3.00 ほう酸ソーダ 0.30 精製水 37.60 メチルパラベン 0.07 (C)香料 適量Example 4 (Hair Dressing Cream) (A) Oil Phase Liquid Lanolin 3.00 Isopropyl Palmitate 15.00 Bead Wax 3.00 Sorbitan Monooleate 2.00 Rescler Oil 25.00 Hydrogenated Rescler Oil 5. 00 Vaseline 6.00 Propylparaben 0.03 (B) Aqueous phase Glycerin 3.00 Sodium borate 0.30 Purified water 37.60 Methylparaben 0.07 (C) Fragrance Suitable amount

【0021】油相(A)、水相(B)を別々に75℃ま
で加熱してから、水相を油相に十分攪拌しながら加え、
さらに、攪拌を続けながら40℃まで冷却し、香料
(C)を加え、ヘアドレッシングクリームを得た。得ら
れたヘアドレッシングクリームは、髪にさっぱり感を与
え、かつ艶を賦与するものであった。
The oil phase (A) and the water phase (B) are separately heated to 75 ° C., and then the water phase is added to the oil phase with sufficient stirring,
Furthermore, it cooled to 40 degreeC, continuing stirring, and added the fragrance | flavor (C) and obtained the hair dressing cream. The obtained hair dressing cream gave a refreshing feeling to the hair and imparted luster.

【0022】実施例5(口紅) 二酸化チタン 4.0 水素添加レスクレラ油 30.0 マカデミアナッツ油 10.0 ビーズワックス 15.0 カルナウバワックス 5.0 セレシン 5.0 トリグリセロールジイソステアレート 10.0 流動パラフィン 4.0 イソプロピルミリステート 15.0 エオシン 2.0Example 5 (lipstick) Titanium dioxide 4.0 Hydrogenated les clera oil 30.0 Macadamia nut oil 10.0 Bead wax 15.0 Carnauba wax 5.0 Ceresin 5.0 Triglycerol diisostearate 10.0 Liquid paraffin 4.0 Isopropyl myristate 15.0 Eosin 2.0

【0023】上記成分を原料にして慣用手段を用いて口
紅を得た。得られた口紅は、のびが良く、唇に湿潤性を
与えた。
A lipstick was obtained using the above ingredients as a raw material by a conventional method. The lipstick obtained spreads well and gives moistness to the lips.

【0024】[0024]

【効果】本発明の化粧料は、皮膚に親和性を有しながら
べとつきがまったくなく、エモリエント性も優れ皮膚に
与えるしっとり感は他の植物油よりはるかに優ってい
る。 また、少量含まれている特殊脂肪酸により、抱水
性がよく皮膚に対する柔軟浸透性に優れた特性を有す
る。さらに、スティック状製品への応用ができ、この場
合も充填剤の分散性に優れ、使用感が非常に滑らかで、
かつ、安全性が高い。
[Effect] The cosmetic composition of the present invention has affinity for the skin, is not sticky at all, has an excellent emollient property, and has a moist feeling far superior to other vegetable oils. In addition, due to the special fatty acid contained in a small amount, it has a good water-holding property and an excellent flexibility and penetrability to the skin. Furthermore, it can be applied to stick-shaped products, and in this case as well, the dispersibility of the filler is excellent, and the feeling of use is very smooth,
And it is highly safe.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 レスクレラ油及び/またはその水素添加
物を含有してなる化粧料。
1. A cosmetic comprising resclere oil and / or a hydrogenated product thereof.
【請求項2】 レスクロリック酸、オーリコリック酸、
デンシポリック酸、及びオレイン酸の異性体を含有して
なる化粧料。
2. Reschloric acid, auricolic acid,
A cosmetic comprising densipolic acid and an isomer of oleic acid.
JP5042089A 1993-02-05 1993-02-05 Cosmetic Pending JPH06227939A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5042089A JPH06227939A (en) 1993-02-05 1993-02-05 Cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5042089A JPH06227939A (en) 1993-02-05 1993-02-05 Cosmetic

Publications (1)

Publication Number Publication Date
JPH06227939A true JPH06227939A (en) 1994-08-16

Family

ID=12626297

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5042089A Pending JPH06227939A (en) 1993-02-05 1993-02-05 Cosmetic

Country Status (1)

Country Link
JP (1) JPH06227939A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009153169A1 (en) * 2008-06-18 2009-12-23 Unilever Plc Compositions for lightening skin color

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009153169A1 (en) * 2008-06-18 2009-12-23 Unilever Plc Compositions for lightening skin color

Similar Documents

Publication Publication Date Title
CA2317471C (en) Dry emollient compositions
US5750121A (en) Color cosmetic composition containing alcohol modified wax
US5503825A (en) Lip balm composition
US4278657A (en) Creamy or milky skin cosmetic compositions containing natural materials as emulsifying agents
CN111096912B (en) Bicontinuous phase type eye and lip makeup remover and preparation method thereof
JPS61501091A (en) Improved vehicle for applying active pharmaceutical ingredients to human skin
JPH08245367A (en) Lipid composition for fragrances and cosmetics and its preparation
JPWO2003015741A1 (en) Moisturizers and cosmetics and external preparations containing humectants
US6284257B1 (en) Cosmetic water emulsion containing at least one vegetable oil
CN114848540A (en) Double-continuous-phase makeup removing composition for cleaning and tendering skin, makeup removing gel and preparation method of makeup removing composition
JPS63192704A (en) Cosmetic
EP1408924A1 (en) Stabilized ascorbic acid, composition, and method of use
US8927034B2 (en) High unsaponifiables and methods of using the same
JPH0521085B2 (en)
JPH075449B2 (en) W / O type lip cosmetic
JPS6231975B2 (en)
JPH06227939A (en) Cosmetic
JP2565516B2 (en) Topical skin
USRE38141E1 (en) Dry emollient compositions
JPS6076543A (en) Oily gel composition
JP2001206817A (en) Oil-in-polyhydric alcohol type thermal substrate
JPH0665045A (en) Skin external preparation
JP4754671B2 (en) Cosmetics
JP3318029B2 (en) Oily external preparation
JPS6111137A (en) Water in oil type emulsion composition