JPH04364118A - Aerosol cosmetic - Google Patents

Aerosol cosmetic

Info

Publication number
JPH04364118A
JPH04364118A JP16618091A JP16618091A JPH04364118A JP H04364118 A JPH04364118 A JP H04364118A JP 16618091 A JP16618091 A JP 16618091A JP 16618091 A JP16618091 A JP 16618091A JP H04364118 A JPH04364118 A JP H04364118A
Authority
JP
Japan
Prior art keywords
ascorbic acid
carbonate
phosphate
added
aerosol
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.)
Withdrawn
Application number
JP16618091A
Other languages
Japanese (ja)
Inventor
Wataru Tokue
徳江 渡
Kenzo Ito
建三 伊藤
Toru Sakai
坂井 透
Tatsuya Okumura
達也 奥村
Mihoko Oba
大庭 美保子
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 JP16618091A priority Critical patent/JPH04364118A/en
Publication of JPH04364118A publication Critical patent/JPH04364118A/en
Withdrawn legal-status Critical Current

Links

Abstract

PURPOSE:To prevent the decomposition of L-ascorbic acid and to obtain an aerosol cosmetic, especially skin-beautifying cosmetic containing L-ascorbic acid in a stably compounded state by compounding L-ascorbic acid with a carbonate and/or a phosphate. CONSTITUTION:The objective aerosol cosmetic containing stably compounded L-ascorbic acid and having skin-beautifying effect is produced by compounding about 0.01-10wt.% of L-ascorbic acid and about 0.01-10wt.% of a carbonate such as an inorganic carbonate (e.g. sodium carbonate and sodium bicarbonate), an organic carbonate (e.g. guanidine carbonate and L-arginine carbonate) and a phosphate such as trisodium phosphate and sodium monohydrogen phosphate.

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、美白作用や肌荒れ改善
作用に優れた化粧料に関するものであり、さらに詳しく
は、L−アスコルビン酸を安定に配合してなるエアゾー
ル化粧料、おもに美白化粧料に関するものである。
[Industrial Field of Application] The present invention relates to cosmetics with excellent whitening effects and skin improvement effects, and more specifically to aerosol cosmetics stably containing L-ascorbic acid, mainly whitening cosmetics. It is related to.

【0002】0002

【従来の技術】従来、L−アスコルビン酸は、皮膚の色
白化等の目的で、化粧料に添加されて来た。しかしなが
ら、L−アスコルビン酸自体がL−アスコルビン酸誘導
体に比べ、化学的に非常に不安定であるため、化粧料に
配合した場合に、経時変化により、または日光などの光
線を受けることにより、L−アスコルビン酸が分解また
は変質し、品質の低下や着色が起こることもあった。こ
れらの防止策として、ウロカニン酸を加える方法(特公
昭57−   49550 号)等が試みられてきた。 これらの試みは相応の成果を上げたのであるが、空気に
よる酸化温度による分解、日光などの光線を受けること
による黄変化現象を防ぐことはできず、安定性も十分な
ものではなかった。
BACKGROUND OF THE INVENTION Conventionally, L-ascorbic acid has been added to cosmetics for the purpose of whitening the skin. However, L-ascorbic acid itself is chemically very unstable compared to L-ascorbic acid derivatives, so when it is added to cosmetics, L-ascorbic acid may deteriorate over time or when exposed to sunlight or other rays. -Ascorbic acid decomposes or changes in quality, resulting in quality deterioration and coloring. As a preventive measure against these problems, a method of adding urocanic acid (Japanese Patent Publication No. 57-49550) has been attempted. Although these attempts had some success, they were unable to prevent decomposition due to the oxidation temperature of the air and yellowing caused by exposure to sunlight and other light rays, and their stability was not sufficient.

【0003】0003

【発明が解決しようとする課題】本発明者らは、このよ
うな事情に鑑み、L−アスコルビン酸が安定に配合でき
ないものかと鋭意研究を重ねた結果、エアゾール剤型に
することにより、L−アスコルビン酸の空気接触による
酸化、光線を受けることによる分解や変質を防ぐことが
できることを見い出した。しかしながら、エアゾール剤
型にするだけでは、温度によるL−アスコルビン酸の分
解はまぬがれず、安定な配合物は得られなかった。
[Problems to be Solved by the Invention] In view of the above circumstances, the present inventors have conducted extensive research to see if L-ascorbic acid can be stably blended. It has been discovered that it is possible to prevent ascorbic acid from being oxidized by contact with air, and from decomposition and deterioration by exposure to light. However, simply forming an aerosol formulation does not prevent L-ascorbic acid from decomposing due to temperature, and a stable formulation cannot be obtained.

【0004】0004

【課題を解決するための手段】本発明者らは、上記の課
題を解決するために鋭意研究を重ねた結果、エアゾール
剤型の化粧料において、炭酸塩及び/又はリン酸塩を配
合することにより温度によるL−アスコルビン酸の分解
を防ぎ、化粧料にL−アスコルビン酸を安定に配合でき
ることを見いだし、この知見に基づいて本発明を完成す
るに到った。
[Means for Solving the Problems] As a result of extensive research in order to solve the above problems, the present inventors have found that carbonates and/or phosphates are incorporated into aerosol-type cosmetics. It was discovered that L-ascorbic acid can be stably blended into cosmetics by preventing decomposition of L-ascorbic acid due to temperature, and based on this knowledge, the present invention was completed.

【0005】すなわち本発明は、炭酸塩及び/又はリン
酸塩とL−アスコルビン酸を配合することを特徴とする
エアゾール化粧料である。
That is, the present invention is an aerosol cosmetic characterized by blending carbonate and/or phosphate with L-ascorbic acid.

【0006】以下、本発明の構成について詳述する。The configuration of the present invention will be explained in detail below.

【0007】本発明に用いられる炭酸塩は、炭酸ナトリ
ウム、重炭酸ナトリウム、炭酸カリウム、重炭酸カリウ
ム、炭酸アンモニウム、重炭酸アンモニウム、炭酸マグ
ネシウム、炭酸カルシウム、炭酸コバルト、炭酸リチウ
ム等の無機炭酸塩、グアニジン炭酸塩、L−アルギニン
炭酸塩、L−リジン炭酸塩等の有機炭酸塩が挙げられ、
リン酸塩の例としては、リン酸三ナトリウム、リン酸一
水素ナトリウム、リン酸二水素ナトリウム、リン酸二水
素カリウム等が用いられる。これらのうち単独または二
種以上混合して使用できる。
Carbonates used in the present invention include inorganic carbonates such as sodium carbonate, sodium bicarbonate, potassium carbonate, potassium bicarbonate, ammonium carbonate, ammonium bicarbonate, magnesium carbonate, calcium carbonate, cobalt carbonate, and lithium carbonate; Examples include organic carbonates such as guanidine carbonate, L-arginine carbonate, and L-lysine carbonate.
Examples of phosphates include trisodium phosphate, sodium monohydrogen phosphate, sodium dihydrogen phosphate, potassium dihydrogen phosphate, and the like. These can be used alone or in combination.

【0008】上記炭酸塩及び/又はリン酸塩の配合量は
単独、あるいは2種以上混合した場合、合計0.01重
量%〜10重量%が好ましい。0.01%未満ではL−
アスコルビン酸の安定性が悪く、10重量%まで配合す
ればL−アスコルビン酸の安定性は良好で問題なく、1
0重量%を超えて配合してもそれ以上の効果の向上は認
められない。
[0008] The amount of the above carbonate and/or phosphate is preferably 0.01% to 10% by weight in total, when used alone or in combination of two or more. If it is less than 0.01%, L-
The stability of ascorbic acid is poor, but if it is added up to 10% by weight, the stability of L-ascorbic acid is good and there is no problem.
Even if it is blended in an amount exceeding 0% by weight, no further improvement in the effect is observed.

【0009】本発明に用いられるL−アスコルビン酸の
配合量は、通常0.01重量%〜10重量%が好ましい
。0.01重量%未満では、L−アスコルビン酸の効果
が発揮されず、また、10重量%を超えて配合しても効
果の向上はみられない。
The amount of L-ascorbic acid used in the present invention is generally preferably 0.01% to 10% by weight. If it is less than 0.01% by weight, the effect of L-ascorbic acid will not be exhibited, and even if it is added in excess of 10% by weight, no improvement in the effect will be observed.

【0010】本発明に用いられるエアゾールの噴射剤は
通常エアゾール製品に用いられる噴射剤であり、具体例
を挙げるとプロパン、イソブタン、ノルマルブタン及び
その混合物である液化石油ガス(以下LPGと略す)、
イソペンタン、ノルマルペンタン、ジメチルエーテル及
びHCFC(ハイドロクロロフルオロカーボン)、HF
C(ハイドロフルオロカーボン)等の液化ガス、炭酸ガ
ス、窒素ガス、酸素ガス等の圧縮ガスである。以上の噴
射剤は単独または混合して使用することも可能である。
The aerosol propellant used in the present invention is a propellant normally used in aerosol products, and specific examples include liquefied petroleum gas (hereinafter abbreviated as LPG), which is propane, isobutane, n-butane, and a mixture thereof;
Isopentane, normal pentane, dimethyl ether and HCFC (hydrochlorofluorocarbon), HF
These are liquefied gases such as C (hydrofluorocarbon), compressed gases such as carbon dioxide gas, nitrogen gas, and oxygen gas. The above propellants can be used alone or in combination.

【0011】本発明はその効果をさまたげない限りにお
いて必要に応じて他の成分、例えばアルコール、多価ア
ルコールなどの保湿剤、界面活性剤、油脂、炭化水素、
脂肪酸、水溶性高分子、粉末、紫外線吸収剤、防腐剤、
薬剤、色剤、香料、その他一般に化粧品業界で汎用され
ている成分を配合することができる。
[0011] The present invention may contain other ingredients as necessary, such as humectants such as alcohol and polyhydric alcohol, surfactants, oils and fats, hydrocarbons, etc., as long as they do not impede the effects.
Fatty acids, water-soluble polymers, powders, ultraviolet absorbers, preservatives,
Drugs, coloring agents, fragrances, and other ingredients commonly used in the cosmetics industry can be blended.

【0012】0012

【発明の効果】本発明のエアゾール化粧料は、炭酸塩及
び/又はリン酸塩を配合することにより、L−アスコル
ビン酸を安定に配合した美白化粧料である。
EFFECTS OF THE INVENTION The aerosol cosmetic of the present invention is a whitening cosmetic that stably contains L-ascorbic acid by incorporating carbonate and/or phosphate.

【0013】[0013]

【実施例】次に実施例によって本発明をさらに詳細に説
明する。本発明はこれにより限定されるものではない。 配合量は重量%である。
EXAMPLES Next, the present invention will be explained in more detail by way of examples. The present invention is not limited thereby. The blending amount is in weight%.

【0014】表1に化粧水スプレータイプの実施例1と
比較例1、2を示す。
Table 1 shows Example 1 and Comparative Examples 1 and 2 of the lotion spray type.

【0015】[0015]

【表1】 実施例1は無機炭酸塩として重炭酸ナトリウムを配合し
たものであり、50℃2カ月保存品、日光暴露30日間
放置品共にL−アスコルビン酸の残存率は高いものであ
った。比較例1は精製水、L−アスコルビン酸、窒素ガ
スの3成分系であり、比較例2は実施例1から重炭酸ナ
トリウムを除いたものであり、どちらもL−アスコルビ
ン酸の残存率は低いものであった。残存率は下式により
求めた。 製法は精製水にL−アスコルビン酸を溶解し、  1、
3−ブチレングリコールにパラオキシ安息香酸メチルを
溶解させたものを加え、その後クエン酸ナトリウム、重
炭酸ナトリウムを溶解させた。これに窒素ガスを噴射剤
として添加した。
[Table 1] Example 1 contains sodium bicarbonate as an inorganic carbonate, and the residual rate of L-ascorbic acid was high in both the product stored at 50° C. for 2 months and the product left exposed to sunlight for 30 days. Comparative Example 1 is a three-component system of purified water, L-ascorbic acid, and nitrogen gas, and Comparative Example 2 is Example 1 without sodium bicarbonate, and both have a low residual rate of L-ascorbic acid. It was something. The residual rate was calculated using the following formula. The manufacturing method is to dissolve L-ascorbic acid in purified water, 1.
A solution of methyl paraoxybenzoate in 3-butylene glycol was added, followed by dissolution of sodium citrate and sodium bicarbonate. Nitrogen gas was added to this as a propellant.

【0016】 (製法)室温で(1) 〜(6) を攪拌溶解し、この
中に(7) 〜(12)を攪拌溶解したものを添加し、
攪拌混合する。これに(13)を噴射剤として添加し、
泡状美白化粧料を得た。
(Production method) (1) to (6) are stirred and dissolved at room temperature, and (7) to (12) are added thereto with stirring,
Stir to mix. Add (13) to this as a propellant,
A foamy whitening cosmetic was obtained.

【0017】 (製法)(1) 〜(6) を加熱混合して70℃とす
る。これに(7) 〜(17)を加熱混合し70とした
もの添加する。その後(18)を加え、ホモミキサーで
均一乳化し冷却する。これを容器に充填し、押し出し用
噴射用として(19)を添加し、美白クリームを得た。
(Manufacturing method) (1) to (6) are heated and mixed to 70°C. To this, (7) to (17) were heated and mixed to make 70 and added. Thereafter, (18) is added, uniformly emulsified using a homomixer, and cooled. This was filled into a container, and (19) was added for injection for extrusion to obtain a whitening cream.

【0018】 (製法)室温で(1) 〜(9) を攪拌溶解し、この
中に攪拌溶解した(10)〜(13)を加える。これを
容器に充填し、押し出し用噴射剤として(14)を添加
し、美白ゼリーを得た。
(Production method) (1) to (9) are stirred and dissolved at room temperature, and (10) to (13) that have been stirred and dissolved are added thereto. This was filled into a container, and (14) was added as an extrusion propellant to obtain a whitening jelly.

【0019】 (製法)室温で (1)〜(6) を攪拌溶解し、この
中に(9) 〜(13)を60℃で攪拌溶解したものを
、室温で混合した(7)、(8) に加え、ホモミキサ
ーで均一に乳化したものを添加する。これに噴射剤とし
て(14)を添加し、泡状美白化粧料(乳液)を得た。
(Production method) (1) to (6) were stirred and dissolved at room temperature, and (9) to (13) were stirred and dissolved therein at 60°C, which was mixed at room temperature to form (7) and (8). ), and add the homogeneous emulsification using a homomixer. (14) was added as a propellant to obtain a foamy whitening cosmetic (emulsion).

【0020】 (製法)室温で(1) 〜(6) を攪拌溶解し、この
中に(7) に(8) 〜(11)を室温で攪拌溶解し
たものを加え、可溶化する。これに(12)を噴射剤と
して添加し、ボディー用美白スプレーを得た。
(Manufacturing method) (1) to (6) are stirred and dissolved at room temperature, and (7) is added to (8) to (11), which have been stirred and dissolved at room temperature, to solubilize. (12) was added as a propellant to obtain a body whitening spray.

【0021】 (製法)(1) に(2) 〜(12)を加熱混合して
、70℃とする。これに(13)〜(19)を加熱混合
し、70℃としたものを添加する。その後(20)を加
え、ホモミキサーで均一乳化し、冷却する。これを容器
に充填し、押し出し用噴射剤として、(21)を添加し
、美白マスクを得た。実施例2〜7はL−アスコルビン
酸が安定に配合されたエアゾール化粧料であった。
(Manufacturing method) (1) and (2) to (12) are heated and mixed to 70°C. To this, (13) to (19) were heated and mixed and the mixture was heated to 70°C and added. Thereafter, (20) was added, uniformly emulsified with a homomixer, and cooled. This was filled into a container, and (21) was added as an extrusion propellant to obtain a whitening mask. Examples 2 to 7 were aerosol cosmetics in which L-ascorbic acid was stably blended.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】炭酸塩及び/又はリン酸塩と、L−アスコ
ルビン酸を配合することを特徴とするエアゾール化粧料
1. An aerosol cosmetic comprising a carbonate and/or phosphate and L-ascorbic acid.
JP16618091A 1990-11-08 1991-06-12 Aerosol cosmetic Withdrawn JPH04364118A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16618091A JPH04364118A (en) 1990-11-08 1991-06-12 Aerosol cosmetic

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2-302856 1990-11-08
JP30285690 1990-11-08
JP16618091A JPH04364118A (en) 1990-11-08 1991-06-12 Aerosol cosmetic

Publications (1)

Publication Number Publication Date
JPH04364118A true JPH04364118A (en) 1992-12-16

Family

ID=26490646

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16618091A Withdrawn JPH04364118A (en) 1990-11-08 1991-06-12 Aerosol cosmetic

Country Status (1)

Country Link
JP (1) JPH04364118A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0940524A (en) * 1995-07-25 1997-02-10 L'oreal Sa Silicone composition containing water reactive activator
EP1033985A1 (en) 1998-09-10 2000-09-13 Avon Products, Inc. Stable ascorbic acid preparation for topical use
JP2003002818A (en) * 2001-06-21 2003-01-08 Mandom Corp Self-suntan cosmetic and its production method
JP2003292431A (en) * 2002-04-02 2003-10-15 Pola Chem Ind Inc Aerosol cosmetic containing bleaching agent
JP2010537976A (en) * 2007-09-04 2010-12-09 コッテ,リミテッド Cosmetic composition containing vitamin C
JP2014521703A (en) * 2011-08-11 2014-08-28 スティーフェル リサーチ オーストラリア ピーティーワイ リミテッド Antioxidant topical composition
WO2016052580A1 (en) * 2014-09-30 2016-04-07 株式会社 Mtg Liquid cosmetic

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0940524A (en) * 1995-07-25 1997-02-10 L'oreal Sa Silicone composition containing water reactive activator
EP1033985A1 (en) 1998-09-10 2000-09-13 Avon Products, Inc. Stable ascorbic acid preparation for topical use
EP1033985B2 (en) 1998-09-10 2008-08-20 Avon Products, Inc. Stable ascorbic acid preparation for topical use
JP2003002818A (en) * 2001-06-21 2003-01-08 Mandom Corp Self-suntan cosmetic and its production method
JP2003292431A (en) * 2002-04-02 2003-10-15 Pola Chem Ind Inc Aerosol cosmetic containing bleaching agent
JP2010537976A (en) * 2007-09-04 2010-12-09 コッテ,リミテッド Cosmetic composition containing vitamin C
JP2014521703A (en) * 2011-08-11 2014-08-28 スティーフェル リサーチ オーストラリア ピーティーワイ リミテッド Antioxidant topical composition
WO2016052580A1 (en) * 2014-09-30 2016-04-07 株式会社 Mtg Liquid cosmetic

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Effective date: 19980903