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JPH01207223A - Solid cosmetics - Google Patents

Solid cosmetics

Info

Publication number
JPH01207223A
JPH01207223A JP3015688A JP3015688A JPH01207223A JP H01207223 A JPH01207223 A JP H01207223A JP 3015688 A JP3015688 A JP 3015688A JP 3015688 A JP3015688 A JP 3015688A JP H01207223 A JPH01207223 A JP H01207223A
Authority
JP
Japan
Prior art keywords
fatty acid
liquid oil
acid ester
solid
starch
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
JP3015688A
Other languages
Japanese (ja)
Inventor
Atsushi Matsushita
篤 松下
Shigesada Momose
重禎 百瀬
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 JP3015688A priority Critical patent/JPH01207223A/en
Publication of JPH01207223A publication Critical patent/JPH01207223A/en
Pending 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/732Starch; Amylose; Amylopectin; Derivatives thereof
    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE:To obtain a solid cosmetic having excellent stability, safety and good feeling on application by combining an N-acylamino acid amide with starch fatty acid ester to set the liquid oil into a solid by gelation. CONSTITUTION:The subject solid cosmetic is composed of (A) an N-acylamino acid amide such as n-lauroyl-L-glutamic acid-alpha,gamma-di-n-butylamide, (1-10wt.%), (B) a starch fatty acid ester (starch hydrolysate of 10-50 average polymerization degree is esterified with a fatty acid) (1-25wt.%) and (C) a liquid oil containing more than 30wt%. of a polar liquid oil such as glyceryl trioctanoate, methylphenylpolysiloxane (40-95wt.%) as essential components. The cosmetic can be readily transferred to the applicator such as a brush, gives smooth feeling on application without rigid touch, moreover, having excellent gloss and clarity.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、固形化粧料に関し、さらに詳しくは、ゲル化
剤としてN−アシルアミノ酸アミドとデンプン脂肪酸エ
ステルとを併用することによって液体油剤をゲル化して
なり、優れた外観を有すると共に安定性、使用感などの
優れた固形化粧料に関するものである。
Detailed Description of the Invention [Field of Industrial Application] The present invention relates to solid cosmetics, and more specifically, the present invention relates to solid cosmetics, and more specifically, to gelling liquid oils by using N-acylamino acid amide and starch fatty acid ester together as gelling agents. The present invention relates to solid cosmetics that are made of solid cosmetics, have an excellent appearance, and are excellent in stability, feel, and the like.

[従来の技術] 従来、固形化粧料には、通常固形油の一種であるワック
スの配合がなされてきた。ワックスは固形化粧料の形状
を保持する上で重要であり、汎用されているが、このよ
うな化粧料ではワックスに由来する固さ、重さによって
、塗布時ののびやなめらかさといった感触を出すことが
難しく、また外観的に透明感のある製品を得ることも困
難であった。
[Prior Art] Conventionally, solid cosmetics have generally been formulated with wax, which is a type of solid oil. Wax is important in maintaining the shape of solid cosmetics and is widely used, but in such cosmetics, the hardness and weight derived from the wax create a feeling of spreadability and smoothness when applied. It was also difficult to obtain a product with a transparent appearance.

これらのワックスの欠点を補い、外観や使用感を向上さ
せる目的で、油ゲル化剤の使用も行われており、つや、
透明感があり、なめらかな感触のある製品を得る為に、
ポリアミド樹脂、12−とドロキシステアリン酸等を利
用することが知られている。
Oil gelling agents are also used to compensate for the shortcomings of these waxes and improve their appearance and feel.
In order to obtain a product that is transparent and has a smooth feel,
It is known to use polyamide resin, 12- and droxystearic acid, and the like.

[発明が解決しようとする課題] しかしながら、従来の固形化粧料において、前記したよ
うな油ゲル化剤を配合した場合、ワックスを用いた固形
化粧料と比較して、感触面においては良好なものが得ら
れるものの、発汗が激しい、強度的に不十分である、透
明感のある製品を製造してもくもりが生じる、等の問題
点があった。
[Problems to be Solved by the Invention] However, when conventional solid cosmetics are blended with an oil gelling agent as described above, they have a better feel compared to solid cosmetics using wax. However, there were problems such as heavy perspiration, insufficient strength, and cloudy appearance even when manufactured with transparent products.

すなわち、強度、成型状態、使用感が良好であると共に
外観的にも十分満足すべき製品は未だ得られていないの
が実情であった。
In other words, the reality is that a product with good strength, molding condition, and usability, as well as a fully satisfactory appearance, has not yet been obtained.

[課題を解決するための手段] 本発明者等は上記課題を解決する為に種々検討した結果
、N−アシルアミノ酸アミドとデンプン脂肪酸エステル
とを併用して液体油剤をゲル化することにより、外観に
優れると同時に使用感や安定性の上からも十分満足しつ
る製品が得られることを見出し、本発明を完成させるに
到った。
[Means for Solving the Problems] As a result of various studies in order to solve the above problems, the present inventors have found that by gelatinizing a liquid oil using a combination of N-acylamino acid amide and starch fatty acid ester, the appearance can be improved. The present inventors have discovered that it is possible to obtain a vine product that has excellent properties and is also fully satisfactory in terms of usability and stability, and has completed the present invention.

すなわち、本発明は、N−アシルアミノ酸アミド、デン
プン脂肪酸エステル、及び液体油剤を必須構成成分とし
てそれぞれ特定割合で含有することを特徴とする固形化
粧料を提供するものである。
That is, the present invention provides a solid cosmetic containing an N-acylamino acid amide, a starch fatty acid ester, and a liquid oil agent as essential components in specific proportions.

以下、本発明の構成について説明する。The configuration of the present invention will be explained below.

本発明において使用されるN−アシルアミノ酸アミドは
、N−アシルアミノ酸誘導体の一種であり、油ゲル化剤
として用いられるものである。化粧料に応用したものと
して、特公昭53−27776号公報に記載された技術
が知られている。N−アシルアミノ酸アミドとして、具
体的には、N−アシルグルタミン酸のジアルキルアミド
の一種であるN−ラウロイル−し−グルタミン酸−α、
γ−ジーn−ブチルアミド(商品名、コアギュランGP
−1;味の素株式会社製)等が使用される。
The N-acylamino acid amide used in the present invention is a type of N-acylamino acid derivative, and is used as an oil gelling agent. As a technique applied to cosmetics, a technique described in Japanese Patent Publication No. 53-27776 is known. Specifically, the N-acylamino acid amide includes N-lauroyl-glutamic acid-α, which is a type of dialkylamide of N-acylglutamic acid;
γ-Di-n-butyramide (trade name, Coagulan GP)
-1; manufactured by Ajinomoto Co., Inc.), etc. are used.

本発明におけるN−アシルアミノ酸アミドの配合量は、
化粧料全量中1〜10重量%の範囲で用いられる。1重
量%より少ない場合は効果か期待し得す、また10重量
%を越えて使用すると他の必須成分との溶解性面で好ま
しくない。
The amount of N-acylamino acid amide in the present invention is:
It is used in an amount of 1 to 10% by weight based on the total amount of cosmetics. If it is less than 1% by weight, some effects can be expected, but if it is used in excess of 10% by weight, it is unfavorable in terms of solubility with other essential components.

次に、本発明において使用されるデンプン脂肪酸エステ
ルは、平均重合度10〜50のデンプン分解物の飽和脂
肪酸エステルであり、例えば、カイハッ化学株式会社製
のレオパールKL等が挙げられる。
Next, the starch fatty acid ester used in the present invention is a saturated fatty acid ester of a starch decomposition product having an average degree of polymerization of 10 to 50, such as Leopard KL manufactured by Kaiha Chemical Co., Ltd., and the like.

本発明におけるデンプン脂肪酸エステルの配合量は、化
粧料全量中1〜25重量%の範囲で用いられる。1重量
%より少ない場合にはN−アシルアミノ酸アミドと併用
する効果がなく、25重量%より多い場合は、ゲルが固
くなりすぎて使用に耐えないものになり、また外観の透
明性が著しく失われてしまう。
The amount of starch fatty acid ester used in the present invention is in the range of 1 to 25% by weight based on the total amount of the cosmetic. If it is less than 1% by weight, there is no effect when used in combination with N-acylamino acid amide, and if it is more than 25% by weight, the gel becomes too hard to be used and the transparency of the appearance is significantly lost. I'll get lost.

また、本発明において必須構成成分である液体油剤は、
N−アシルアミノ酸アミドの溶解性に慢れ、強固で安定
なゲルを生成するものが好ましく、例えば、トリオクタ
ン酸グリセリル、イソステアリン酸トリグリセリル、ト
リイソステアリン酸ジグリセリル、ジステアリン酸ジグ
リセリル、マカデミアンナッツ油、とマシ油、精製ホホ
バ油等のエステル油、メチルフェニルポリシロキサン等
のシリコーン油等の極性液体油が特に好適である。この
他、流動パラフィン、スクワラン等の炭化水素類等の無
極性油剤の場合、単独ではN−アシルアミノ酸アミドの
溶解性が悪く、安定なゲルが生成しにくいが、前記極性
液体油と併用することにより、良好な製品を得ることが
できる。この場合には、液体油剤において、極性液体油
の占める割合を30重61%以上とすることが必要であ
り、30重量%より少ない場合には安定なゲルが形成で
きず、強度面で劣るようになり、好ましくない。
In addition, the liquid oil agent which is an essential component in the present invention is
N-acyl amino acid amides that have good solubility and form a strong and stable gel are preferred, such as glyceryl trioctanoate, triglyceryl isostearate, diglyceryl triisostearate, diglyceryl distearate, and macadamian nut oil. Particularly suitable are polar liquid oils such as ester oils such as mustard oil, refined jojoba oil, and silicone oils such as methylphenylpolysiloxane. In addition, non-polar oils such as hydrocarbons such as liquid paraffin and squalane have poor solubility in N-acylamino acid amides and are difficult to form stable gels when used alone, but they can be used in combination with the polar liquid oil. As a result, good products can be obtained. In this case, it is necessary to make the proportion of polar liquid oil in the liquid oil agent at least 30% by weight and 61%; if it is less than 30% by weight, a stable gel cannot be formed and the strength may be deteriorated. , which is not desirable.

本発明における液体油剤の配合量は、化粧料全量中40
〜95重量%の範囲で適宜選択される。40重量%より
少ない場合には、優れたゲルが形成できず、また95%
を越えた場合にも、強度等の面で十分でない。
The amount of liquid oil in the present invention is 40% of the total amount of cosmetics.
It is appropriately selected within the range of 95% by weight. If it is less than 40% by weight, an excellent gel cannot be formed, and if it is less than 95%
Even if it exceeds this, it is not sufficient in terms of strength etc.

本発明の固形化粧料は、上記三成分を必須構成成分とし
て含有するものであるが、これらの成分によるゲル形成
性、安定性及び透明性に及ぼす効果について実証する。
The solid cosmetic of the present invention contains the above three components as essential components, and the effects of these components on gel formation, stability, and transparency will be demonstrated.

表1に組成を示す試料■〜■を製造し、スティック状に
成型して、ゲル強度、及び発汗の有無について判定した
Samples ① to ② whose compositions are shown in Table 1 were manufactured, molded into stick shapes, and evaluated for gel strength and the presence or absence of sweating.

判定基準 ◎:非常に良好 ○:良好 △:やや悪い X:悪い 表! (製法) A(1)、(3)、(4)、(6)を130〜135℃
にて加熱溶解する(試料■はこの工程を除く)。
Judgment criteria ◎: Very good ○: Good △: Fairly bad X: Bad! (Manufacturing method) A (1), (3), (4), (6) at 130-135°C
Dissolve by heating (this step is excluded for sample ①).

BAを100℃に冷却し、(匂、(5)を加えて溶解す
る。
Cool BA to 100°C, add (5) and dissolve.

CBを脱気した後、型に流し込み冷却する。After degassing the CB, it is poured into a mold and cooled.

表1の結果から明らかな如く、N−アシルアミノ酸アミ
ドを用いない場合(試料■)は、強度が極端に小さく、
安定性も劣るものであった。またデンプン脂肪酸エステ
ルを用いない場合(試料■)は、強度も不十分であるが
、発汗かひどく、12−とドロキシステアリン酸を添加
(試料■)してもあまり効果が見られなかフた。これに
対し、N−アシルアミノ酸アミドとデンプン脂肪酸エス
テルを併用した場合(試料■、■)は、ゲル強度に優れ
ると共に発汗もなく、安定性の上でも最も良好なもので
あり、また非常に高い透明感を有するものであった。さ
らに、ゲル化剤としてN−アシルアミノ酸アミドとデン
プン脂肪酸エステルを併用しても、液体油剤として無極
性油剤の流動パラフィンが多量に入った場合(試料■)
は、発汗が生じやすく経時安定性の上でも満足できない
ものであると共に、強度も不充分で、崩れやすいもので
あったが、流動パラフィンの添加量を抑え、極性液体油
であるトリイソステアリン酸ジグリセリルの割合を多く
した場合(試料■)は、発汗が生じにくく、また強度も
非常に優れたものであった。
As is clear from the results in Table 1, when N-acylamino acid amide is not used (sample ■), the strength is extremely low;
The stability was also poor. In addition, when starch fatty acid ester was not used (sample ■), the strength was insufficient, but the sweating was severe, and even when 12- and droxystearic acid were added (sample ■), there was no noticeable effect. . On the other hand, when N-acylamino acid amide and starch fatty acid ester were used together (Samples ■ and ■), the gel strength was excellent, there was no sweating, the stability was the best, and the gel strength was very high. It had a transparent feel. Furthermore, even if N-acylamino acid amide and starch fatty acid ester were used together as a gelling agent, a large amount of liquid paraffin, a non-polar oil agent, entered the liquid oil agent (sample ■).
However, by reducing the amount of liquid paraffin added and using diisostearic acid, which is a polar liquid oil, When the proportion of glyceryl was increased (Sample ■), sweating was less likely to occur and the strength was also very good.

すなわち、本発明の必須構成成分を特定割合で併用する
ことによって、ゲル形成性、安定性及び透明性が顕著に
向上することがわかった。
That is, it has been found that gel formation, stability, and transparency are significantly improved by using the essential components of the present invention in specific proportions.

本発明に係る固形化粧料は、上記の如<N−アシルアミ
ノ酸アミド、デンプン脂肪酸エステル、及び液体油剤を
特定の組成割合で含有するものであり、スティック状又
は皿状の製品として利用される。
The solid cosmetic according to the present invention contains the above-mentioned N-acylamino acid amide, starch fatty acid ester, and liquid oil in a specific composition ratio, and is used as a stick-shaped or plate-shaped product.

また、本発明の固形化粧料は、化粧目的・製品形態等に
応じて、樹脂、顔料、香料、酸化防止剤、防腐剤、紫外
線吸収剤等を配合し、その添加効果を発揮するように調
製しうるものである。例えば、樹脂の一種であるロジン
酸ペンタエリトリットは、本発明の固形化粧料を透明タ
イプのものにする場合に、透明感を向上させ、また、光
沢、化粧もち等の使用感をより良好ならしめることがで
き、化粧料全量中最大30重量%までの範囲で添加する
ことができる。
In addition, the solid cosmetic of the present invention is formulated with resins, pigments, fragrances, antioxidants, preservatives, ultraviolet absorbers, etc., depending on the cosmetic purpose and product form, etc., and is prepared to exhibit the effects of the addition. It is possible. For example, pentaerythritol rosin acid, which is a type of resin, improves the transparency when making the solid cosmetic of the present invention into a transparent type, and also improves the usability such as gloss and makeup retention. It can be added in an amount up to 30% by weight based on the total amount of cosmetics.

[実施例] 次に、本発明について実施例を挙げてさらに説明する。[Example] Next, the present invention will be further explained by giving examples.

尚、これらは本発明を何ら限定するものではない。Note that these do not limit the present invention in any way.

実施例 [11スティック状口紅 (処方)             (重量%)(1)
N−ラウロイル−し−グルタミン  5.5酸−α、γ
−ジーn−ブチルアミド (2)デンプン脂肪酸エステル     6.0(3)
12−とドロキシステアリン酸1.5(4)スクワラン
            5.0(5)トリオクタン酸
グリセリル    12.516)トリイソステアリン
酸ジグリセリ 53.7(7) ロジン酸ペンタエリト
リット   10.0(8)酸化防止剤       
     0.05(9)  防腐剤        
      0.0500)酸化チタン       
     3.0(1リ 赤色202号       
    0.302)赤色226号         
  1.003)  黄色4号アルミニウムレーキ  
  1.2(14)  香料            
   0・2(製法) A  (1)、(4)、(′7)を130〜135℃に
て加熱溶解する。
Example [11 Stick-shaped lipstick (formulation) (wt%) (1)
N-lauroyl-shi-glutamine 5.5 acid-α, γ
-J-n-butyramide (2) Starch fatty acid ester 6.0 (3)
12- and droxystearic acid 1.5(4) Squalane 5.0(5) Glyceryl trioctanoate 12.516) Diglyceryl triisostearate 53.7(7) Pentaerythritol rosin acid 10.0(8) Antioxidant agent
0.05(9) Preservative
0.0500) Titanium oxide
3.0 (1ri red No. 202
0.302) Red No. 226
1.003) Yellow No. 4 aluminum rake
1.2 (14) Fragrance
0.2 (Production method) A (1), (4), and ('7) are heated and dissolved at 130 to 135°C.

BAを110℃以下に冷却、し、(2)、(3)、但)
、(9)を添加、溶解する。
Cool BA to 110°C or less, (2), (3), but)
, (9) is added and dissolved.

CBに(10)〜03)を分散する。Disperse (10) to 03) in CB.

DCを脱気した後、師)を加え、容器に流し込み冷却す
る。
After degassing the DC, add the liquid, pour into a container, and cool.

比較例[+] (処方)             (重量%)(1)
  マイクロクリスタリンワックス  10.0(2)
  ショ糖脂肪酸エステル      13.0(3)
  ロジン酸ペンタエリトリット    17.0(4
) ヒマシ油             9・0(均 
ステアリン酸イソセチル     17.0(6)  
ジブカン酸プロピレングリコール 20.0(71トリ
オクタン酸グリセリル    8.2(8)酸化防止剤
           0.05(9)防腐剤    
          0.0500)酸化チタン   
         3.0(ロ)赤色202号    
      0.302)赤色226号       
    19口03)黄色4号アルミニウムレーキ  
  1.2(14)  香料            
   0,2(製法) A(1)、(3)〜(7)を120℃にて加熱溶解する
Comparative example [+] (Formulation) (Weight%) (1)
Microcrystalline wax 10.0 (2)
Sucrose fatty acid ester 13.0 (3)
Rosin acid pentaerythritol 17.0 (4
) Castor oil 9.0 (average
Isocetyl stearate 17.0(6)
Propylene glycol dibucanate 20.0 (71 glyceryl trioctanoate 8.2 (8) antioxidant 0.05 (9) preservative
0.0500) Titanium oxide
3.0 (b) Red No. 202
0.302) Red No. 226
19 mouth 03) Yellow No. 4 aluminum rake
1.2 (14) Fragrance
0,2 (Production method) A(1), (3) to (7) are heated and dissolved at 120°C.

BAを100℃に冷却し、(2)、(8)、(9)を添
加、溶解する。
Cool BA to 100°C, add and dissolve (2), (8), and (9).

CBに00】〜63)を分散する。Disperse 00]~63) in CB.

DCを脱気した後、(川を加え、容器に流し込み冷却す
る。
After degassing the DC, add water and pour into a container to cool.

上記の如くして得られた実施例[11の口紅は、ワック
スを使用しない為に塗布時に固さを感じさせず、なめら
かでのびが良いものであると共に、口唇に優れた光沢を
付与するものであった。これに対し、ワックスを用いた
比較例El]の口紅は、塗布時に固さ、重さを感じるも
のであり、のび、なめらかさの点でも不十分なものであ
った。
The lipstick of Example [11] obtained as above does not use wax, so it does not feel hard when applied, is smooth and spreads well, and gives an excellent gloss to the lips. Met. On the other hand, the lipstick of Comparative Example El] using wax felt hard and heavy when applied, and was unsatisfactory in spreadability and smoothness.

実施例 [2]  スティック状透明口紅(処方)  
           (重量%)(1)  N−ラウ
ロイル−L−グルタミン  5.5酸−α、γ−ジーn
−ブチルアミド (2ン  デンプン脂肪酸エステル     5.0(
3112−とドロキシステアリン酸  1.5(4) 
トリイソステアリン酸ジグリセリ 77.65ル (5)  ロジン酸ペンタエリトリット    10.
0(6)  酸化防止剤           0.0
5(7)  防腐剤              0.
05(8)赤色223号          0.05
(9)  香料               0.2
(製法) A  (1)、(4)、(5)を130〜135℃にて
加熱溶解する。
Example [2] Stick-shaped transparent lipstick (prescription)
(% by weight) (1) N-lauroyl-L-glutamine 5.5 acid-α, γ-gin
-Butyramide (2 starch fatty acid ester 5.0)
3112- and droxystearic acid 1.5 (4)
Diglyceride triisostearate 77.65L (5) Pentaerythritol rosin acid 10.
0(6) Antioxidant 0.0
5(7) Preservative 0.
05 (8) Red No. 223 0.05
(9) Fragrance 0.2
(Manufacturing method) A (1), (4), and (5) are heated and dissolved at 130 to 135°C.

BAを110℃以下に冷却し、(2)、(3)、(句、
(7)を添加、溶解する。
Cool BA to below 110°C, (2), (3), (phrase,
Add and dissolve (7).

CBに(8)を分散する。Distribute (8) to CB.

DCを脱気した後、(9)を加え、容器に流し込み冷却
する。
After degassing the DC, add (9), pour into a container, and cool.

以上の如くして得られた実施例[2]の透明口紅は、外
観の透明性に優れ、安定であり、また使用時ののびも良
く、なめらかな使用感を有するものであフた。しかも、
口唇に非常に良好な光沢を付与するものであった。
The transparent lipstick of Example [2] obtained as described above had excellent transparency in appearance, was stable, spread well during use, and had a smooth feeling of use. Moreover,
It imparted very good gloss to the lips.

実施例[3]ススティック透明口紅 (処方)             (重量%)(1)
  N−ラウロイル−し−グルタミン 4,0酸−α、
γ−ジーn−ブチルアミド (2)  デンプン脂肪酸エステル     10.0
(3)  メチルフェニルポリシロキサン  82.6
5(4)酸化防止剤            0.05
(5)防腐剤              0.05(
6)  フィタントリオール        3.0(
力 赤色202号           0.05(8
)香料               0.2(製法) A  (1)、(3)、(0を適量のメチルアルコール
に溶解し、攪拌混合後、メチルアルコールを除く。
Example [3] Stick transparent lipstick (formulation) (wt%) (1)
N-lauroyl-shi-glutamine 4,0 acid-α,
γ-di-n-butylamide (2) Starch fatty acid ester 10.0
(3) Methylphenylpolysiloxane 82.6
5(4) Antioxidant 0.05
(5) Preservative 0.05 (
6) Phytantriol 3.0 (
Power Red No. 202 0.05 (8
) Fragrance 0.2 (Production method) A (1), (3), (Dissolve 0 in an appropriate amount of methyl alcohol, stir and mix, then remove the methyl alcohol.

BAに(2)、(4)、((ロ)を加え、110℃にて
加熱溶解する。
Add (2), (4), and ((b) to BA and heat and dissolve at 110°C.

CBに(7)を分散する。Distribute (7) to CB.

DCを脱気した後、(8)を加え、容器に流し込み冷却
する。
After degassing the DC, add (8), pour into a container, and cool.

以上の如くして得られた実施例[3]の透明口紅は、外
観の透明性に優れると共に経時安定性も良く、のび、な
めらかさの優れたものであった。また、塗布後の口唇に
非常に良好な光沢を付与するものであった。
The transparent lipstick of Example [3] obtained as described above had excellent transparency in appearance, good stability over time, and excellent spreadability and smoothness. Moreover, it imparted very good gloss to the lips after application.

実Jei例[4] 7111状[)紅 (処方)             (重量%)(1)
  N−ラウロイル−し−グルタミン  3.0酸−α
、γ−ジーn−ブチルアミド (2)  デンプン脂肪酸エステル     5.0(
3)トリオクタン酸グリセリル    15.0(4)
 トリイソステアリン酸ジグリセリ 56.6ル (5)  ロジン酸ペンタエリトリット   20.0
((へ)酸化防止剤           0.05(
7)防腐剤              0.05(8
)赤色202号          0.1(9ン 香
料               0.2(製法) A  (1)、(4)、(5)を130〜135℃にて
加熱溶解する。
Actual Jei example [4] 7111 condition [) Beni (prescription) (wt%) (1)
N-lauroyl-shi-glutamine 3.0 acid-α
, γ-di-n-butylamide (2) Starch fatty acid ester 5.0 (
3) Glyceryl trioctanoate 15.0 (4)
Diglyceryl triisostearate 56.6 l(5) Pentaerythritol rosin acid 20.0
((f) Antioxidant 0.05(
7) Preservative 0.05 (8
) Red No. 202 0.1 (9 N) Fragrance 0.2 (Production method) A Heat and dissolve (1), (4), and (5) at 130 to 135°C.

BAを110℃以下に冷却し、(2)、(3)、(6)
、(力を加え、溶解する。
Cool BA to 110°C or less, (2), (3), (6)
, (Apply force and dissolve.

CBに(8)を分散する。Distribute (8) to CB.

DCを脱気した後、(9)を加え、全血に流し込み冷却
する。
After degassing the DC, (9) is added, poured into whole blood, and cooled.

上記の如くして得られた実施例[4]の皿状口紅は、紅
筆にとる際のとれが良く、使用性が良好なものであると
共に、なめらかでのびの良い使用感を有し、塗布後の口
唇に優れた光沢を付与するものであった。
The dish-shaped lipstick of Example [4] obtained as described above has good ease of use when applied with a red brush, and has a smooth and easy-to-apply feel, It imparted excellent gloss to the lips after application.

[発明の効果コ 以上詳述した如く、本発明の固形化粧料は、ゲル化剤と
してN−アシルアミノ酸アミドとデンプン脂肪酸エステ
ルとを併用することによって液体油剤をゲル化させて得
られるものである。
[Effects of the Invention] As detailed above, the solid cosmetic of the present invention is obtained by gelling a liquid oil by using N-acylamino acid amide and starch fatty acid ester together as a gelling agent. .

本発明により、ワックスを使用することなく、適度な強
度をもち、発汗がない等固化成型状態が良好であると共
に、塗布具へのどれや使用時ののびが良く、固さを感じ
ないなめらかな使用感を有し、しかも、優れた光沢、透
明感をも有する外観の優れた固形化粧料を得ることが可
能となったのである。
With the present invention, without the use of wax, it has moderate strength, no sweating, etc., and has a good hardening and molding state. It has now become possible to obtain a solid cosmetic that is easy to use, has excellent gloss and transparency, and has an excellent appearance.

以  上 出願人 株式会社 小林コーセーthat's all Applicant: Kobayashi Kose Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] (1)N−アシルアミノ酸アミド1〜10重量%と、デ
ンプン脂肪酸エステル1〜25重量%と、極性液体油を
30重量%以上含む液体油剤40〜95重量%とを必須
構成成分として含有することを特徴とする固形化粧料。
(1) Contains 1-10% by weight of N-acylamino acid amide, 1-25% by weight of starch fatty acid ester, and 40-95% by weight of a liquid oil containing 30% by weight or more of polar liquid oil as essential components. Solid cosmetics featuring:
JP3015688A 1988-02-12 1988-02-12 Solid cosmetics Pending JPH01207223A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3015688A JPH01207223A (en) 1988-02-12 1988-02-12 Solid cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3015688A JPH01207223A (en) 1988-02-12 1988-02-12 Solid cosmetics

Publications (1)

Publication Number Publication Date
JPH01207223A true JPH01207223A (en) 1989-08-21

Family

ID=12295891

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3015688A Pending JPH01207223A (en) 1988-02-12 1988-02-12 Solid cosmetics

Country Status (1)

Country Link
JP (1) JPH01207223A (en)

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02180805A (en) * 1988-12-29 1990-07-13 Shiseido Co Ltd External drug for skin
US5284649A (en) * 1992-09-29 1994-02-08 The Procter & Gamble Company Deodorant gel sticks containing 1-hydroxy pyridinethione active
US5429816A (en) * 1992-05-12 1995-07-04 Procter & Gamble Antiperspirant gel stick compositions
US5516511A (en) * 1994-05-06 1996-05-14 The Procter & Gamble Company Antiperspirant gel compositions comprising chelators
US5552136A (en) * 1994-05-25 1996-09-03 The Procter & Gamble Company Gel stick compositions comprising optically enriched gellants
US5635165A (en) * 1995-09-27 1997-06-03 Helene Curtis, Inc. Antiperspirant deodorant compositions
EP0811369A2 (en) * 1996-06-04 1997-12-10 Shiseido Company Limited A cosmetic
US5733534A (en) * 1993-04-27 1998-03-31 The Procter & Gamble Company Antiperspirant stick compositions exhibiting improved wash-off performance
US5744130A (en) * 1996-12-20 1998-04-28 The Procter & Gamble Company Antiperspirant gel-solid stick compositions substantially free of select polar solvents
US5750096A (en) * 1996-12-20 1998-05-12 The Procter & Gamble Company Low residue antiperspirant gel-solid stick compositions containing select gellants
US5776494A (en) * 1996-12-20 1998-07-07 The Procter & Gamble Company Pharmaceuticals compositions containing gellants in the form of alkyl amides of di-and tri-carboxylic acids
US5840286A (en) * 1996-12-20 1998-11-24 Procter & Gamble Company Methods of making low residue antiperspirant gel-solid stick compositions
US5840287A (en) * 1996-12-20 1998-11-24 Procter & Gamble Company Antiperspirant compositions containing gellants in the form of alkyl amides of di- and tri-carboxylic acids
US5840288A (en) * 1996-12-20 1998-11-24 Procter & Gamble Company Antiperspirant gel-solid stick composition containing a modified silicone carrier
US5840883A (en) * 1995-04-05 1998-11-24 Chiba Flour Milling Co., Ltd. Dextrin ester of fatty acids and use thereof
US5846520A (en) * 1996-12-20 1998-12-08 Procter & Gamble Company Antiperspirant gel-solid stick compositions containing select fatty acid gellants
US5849276A (en) * 1996-12-20 1998-12-15 Procter & Gamble Antiperspirant gel-solid stick compositions containing select nucleating agents
US6171601B1 (en) 1996-12-20 2001-01-09 The Procter & Gamble Company Low residue antiperspirant gel-solid stick compositions
US6190673B1 (en) 1996-12-20 2001-02-20 The Procter & Gamble Company Gel compositions containing gellants in the form of alkyl amides of tri-carboxylic acids
US6423324B1 (en) 2000-06-20 2002-07-23 Cosmolab, Inc. Temperature-stable polyamide resin-based composition, and products
WO2004105707A1 (en) * 2003-05-28 2004-12-09 Ajinomoto Co. Inc. Oil based gel composition
JP2010132562A (en) * 2008-12-02 2010-06-17 Kao Corp Stick-shaped oily cosmetic
JP2016124863A (en) * 2014-12-26 2016-07-11 株式会社コーセー Oily solid cosmetic
JP2021091813A (en) * 2019-12-11 2021-06-17 株式会社 資生堂 Oil gel composition and cosmetic

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02180805A (en) * 1988-12-29 1990-07-13 Shiseido Co Ltd External drug for skin
US5429816A (en) * 1992-05-12 1995-07-04 Procter & Gamble Antiperspirant gel stick compositions
US5284649A (en) * 1992-09-29 1994-02-08 The Procter & Gamble Company Deodorant gel sticks containing 1-hydroxy pyridinethione active
US5733534A (en) * 1993-04-27 1998-03-31 The Procter & Gamble Company Antiperspirant stick compositions exhibiting improved wash-off performance
US5516511A (en) * 1994-05-06 1996-05-14 The Procter & Gamble Company Antiperspirant gel compositions comprising chelators
US5552136A (en) * 1994-05-25 1996-09-03 The Procter & Gamble Company Gel stick compositions comprising optically enriched gellants
US5840883A (en) * 1995-04-05 1998-11-24 Chiba Flour Milling Co., Ltd. Dextrin ester of fatty acids and use thereof
US5635165A (en) * 1995-09-27 1997-06-03 Helene Curtis, Inc. Antiperspirant deodorant compositions
EP0811369A2 (en) * 1996-06-04 1997-12-10 Shiseido Company Limited A cosmetic
EP0811369A3 (en) * 1996-06-04 1998-12-02 Shiseido Company Limited A cosmetic
US5840287A (en) * 1996-12-20 1998-11-24 Procter & Gamble Company Antiperspirant compositions containing gellants in the form of alkyl amides of di- and tri-carboxylic acids
US5849276A (en) * 1996-12-20 1998-12-15 Procter & Gamble Antiperspirant gel-solid stick compositions containing select nucleating agents
US5776494A (en) * 1996-12-20 1998-07-07 The Procter & Gamble Company Pharmaceuticals compositions containing gellants in the form of alkyl amides of di-and tri-carboxylic acids
US5840288A (en) * 1996-12-20 1998-11-24 Procter & Gamble Company Antiperspirant gel-solid stick composition containing a modified silicone carrier
US5750096A (en) * 1996-12-20 1998-05-12 The Procter & Gamble Company Low residue antiperspirant gel-solid stick compositions containing select gellants
US5744130A (en) * 1996-12-20 1998-04-28 The Procter & Gamble Company Antiperspirant gel-solid stick compositions substantially free of select polar solvents
US5846520A (en) * 1996-12-20 1998-12-08 Procter & Gamble Company Antiperspirant gel-solid stick compositions containing select fatty acid gellants
US5840286A (en) * 1996-12-20 1998-11-24 Procter & Gamble Company Methods of making low residue antiperspirant gel-solid stick compositions
US6171601B1 (en) 1996-12-20 2001-01-09 The Procter & Gamble Company Low residue antiperspirant gel-solid stick compositions
US6190673B1 (en) 1996-12-20 2001-02-20 The Procter & Gamble Company Gel compositions containing gellants in the form of alkyl amides of tri-carboxylic acids
US6423324B1 (en) 2000-06-20 2002-07-23 Cosmolab, Inc. Temperature-stable polyamide resin-based composition, and products
WO2004105707A1 (en) * 2003-05-28 2004-12-09 Ajinomoto Co. Inc. Oil based gel composition
JP2010132562A (en) * 2008-12-02 2010-06-17 Kao Corp Stick-shaped oily cosmetic
JP2016124863A (en) * 2014-12-26 2016-07-11 株式会社コーセー Oily solid cosmetic
JP2021091813A (en) * 2019-12-11 2021-06-17 株式会社 資生堂 Oil gel composition and cosmetic

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