JPH0363208A - Cosmetic - Google Patents

Cosmetic

Info

Publication number
JPH0363208A
JPH0363208A JP20070789A JP20070789A JPH0363208A JP H0363208 A JPH0363208 A JP H0363208A JP 20070789 A JP20070789 A JP 20070789A JP 20070789 A JP20070789 A JP 20070789A JP H0363208 A JPH0363208 A JP H0363208A
Authority
JP
Japan
Prior art keywords
cosmetic
ascorbic acid
antiseptic
ester
stability
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
JP20070789A
Other languages
Japanese (ja)
Inventor
Yoko Sato
陽子 佐藤
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 JP20070789A priority Critical patent/JPH0363208A/en
Publication of JPH0363208A publication Critical patent/JPH0363208A/en
Pending legal-status Critical Current

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  • Cosmetics (AREA)

Abstract

PURPOSE:To obtain an ascorbic acid phosphate ester-containing cosmetic providing excellent antiseptic and mildewproofing effects without damaging stability, etc., of the ester by blending the ascorbic acid phosphoric ester-containing cosmetic with phenoxyethanol as an antiseptic mildewproofing agent. CONSTITUTION:A cosmetic which contains preferably >=0.01wt.% ascorbic acid phosphoric ester being more stable than ascorbic acids which have been used as an active ingredient of cosmetic for fair skin and beauty and having beautifying effects but requires alkalinity of cosmetic because of instability of aqueous solution in a range of pH of neutrality to acidity, further contains preferably >=1wt.% water and has pH>=7.0, especially pH7.0-9.0 is blended with preferably 0.01-2.0wt.% phenoxyethanol as an antiseptic mildewproofing agent to give the above-mentioned cosmetic which has excellent stability in a range of alkalinity and provides antiseptic and mildewproofing effects and high stability to the skin without damaging solubility and stability of the ester and touch of cosmetic in use.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、含有成分であるアスコルビン酸リン酸エステ
ルが安定で、かつ防腐防黴効果に優れた化粧料に関する
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a cosmetic composition in which the ascorbic acid phosphate ester contained therein is stable and has excellent antiseptic and antifungal effects.

[従来の技術及びその課題] 従来、アスコルビン酸やその脂肪酸エステルに美白効果
があることが知られており、美白化粧料の有効成分とし
て用いられていた。しかし、これらの化合物は不安定で
あり、また美白効果も充分ではないという問題があった
[Prior art and its problems] Ascorbic acid and its fatty acid esters have been known to have a whitening effect and have been used as active ingredients in whitening cosmetics. However, these compounds have problems in that they are unstable and do not have sufficient whitening effects.

そこで、より安定かつ美白効果にも優れ、化粧料成分と
して好ましく使用できるアスコルビン酸リン酸エステル
が開発されている(特公昭44−31237号公報、特
開昭62−129212号公報、特開昭62−2985
08号公報、特開昭63−243014号公報等)。し
かし、このアスコルビン酸リン酸エステルも、水溶液の
pHが中性〜酸性の領域では不安定であり、これを含有
する化粧料はアルカリ性とする必要があった。
Therefore, ascorbic acid phosphate ester has been developed which is more stable and has excellent whitening effect and can be preferably used as a cosmetic ingredient (Japanese Patent Publication No. 44-31237, Japanese Patent Application Laid-open No. 62-129212, Japanese Patent Application Laid-open No. 62-129212, Japanese Patent Application Laid-Open No. 62-129212, -2985
No. 08, JP-A No. 63-243014, etc.). However, this ascorbic acid phosphate ester is also unstable when the pH of the aqueous solution is in the neutral to acidic range, and cosmetics containing it have to be alkaline.

一方、化粧料の防腐防黴剤としては、化粧料中で安定で
あり、他の成分に悪影響を及ぼさず、皮溝安全性が高く
、少量で効果が充分に発押されることが要求される。
On the other hand, as a preservative and antifungal agent for cosmetics, it is required to be stable in cosmetics, not have a negative effect on other ingredients, have high skin groove safety, and be sufficiently effective with a small amount. .

しかしながら、化粧料に一般に用いられる防腐防黴剤の
うち、安息香酸、デヒドロ酢酸、サリチル酸、それらの
塩類等の防腐防黴効果は酸性領域で有効なもので、アル
カリ性領域では効果を示さないため、上記アスコルビン
酸リン酸エステル含有化粧料には適用できないものであ
る。またバラオキシ安息香酸エステル類は優れた防腐防
黴効果を有し、最も使用頻度の高いものであるが、アル
カリ性領域では加水分解を受けやすい(J、 Soc。
However, among the preservatives and fungicides commonly used in cosmetics, benzoic acid, dehydroacetic acid, salicylic acid, and their salts are effective in the acidic range and are not effective in the alkaline range. It cannot be applied to the above ascorbic acid phosphate-containing cosmetics. In addition, roseoxybenzoic acid esters have excellent antiseptic and antifungal effects and are the most frequently used ones, but they are susceptible to hydrolysis in alkaline regions (J, Soc.

Cosmet、 Chem、、 25.495−506
(1974))ことが知られており、また極性油等の多
い系では極性油に溶解して水系中の濃度が低くなってし
まい、充分に効果が発揮されない等の問題があった。ま
たエタノール、プロピレングリコール等のグリコール類
を防腐剤として用いた場合、充分な効果を発揮する量を
配合すると、アスコルビン酸リン酸エステルが析出した
り、使用感触を損なう等の問題があった。
Cosmet, Chem, 25.495-506
(1974)), and in systems containing a large amount of polar oil, etc., there are problems such as dissolving in the polar oil and lowering the concentration in the aqueous system, resulting in insufficient effectiveness. Furthermore, when glycols such as ethanol and propylene glycol are used as preservatives, there are problems such as precipitation of ascorbic acid phosphate ester and impairing the feel of the product when used in an amount sufficient to achieve a sufficient effect.

[課題を解決するための手段] かかる実情において本発明者らは、皮膚安全性が高く、
アルカリ性領域で安定かつ防腐防黴効果が高く、アスコ
ルビン酸リン酸エステルの溶解性及び安定性並びに化粧
料の使用感触に悪影響を与えない防腐防黴剤について鋭
意研究を行なった結果、フェノキシエタノールがこれら
の条件を満足するものであることを見出し、本発明を完
成した。
[Means for Solving the Problems] Under these circumstances, the present inventors have developed a method that has high skin safety and
As a result of intensive research into a preservative and fungicide that is stable in an alkaline region and has a high preservative and antifungal effect, and does not have a negative effect on the solubility and stability of ascorbic acid phosphate ester or the feel of cosmetics, we found that phenoxyethanol is a highly effective preservative and antifungal agent. The present invention was completed based on the discovery that the above conditions were satisfied.

すなわち本発明は、アスコルビン酸リン酸エステルまた
はその塩及びフェノキシエタノールを含有することを特
徴とする化粧料を提供するものである。
That is, the present invention provides a cosmetic material containing ascorbic acid phosphate ester or a salt thereof and phenoxyethanol.

本発明において、アスコルビン酸リン酸エステルの塩と
しては例えばマグネシウム塩、ナトリウム塩、カリウム
塩、カルシウム塩、トリエタノールアミン塩等が挙げら
れ、特に好ましいものとしてL−アスコルビン酸−2−
リン酸エステルマグネシウム塩が挙げられる。本発明化
粧料中のアスコルビン酸リン酸エステルまたはその塩の
含有量としては特に限定されないが、0.01重量%以
上であることが好ましい。
In the present invention, examples of salts of ascorbic acid phosphate include magnesium salts, sodium salts, potassium salts, calcium salts, triethanolamine salts, etc., and particularly preferred ones include L-ascorbic acid-2-
Examples include magnesium phosphate ester salts. The content of ascorbic acid phosphate or its salt in the cosmetic of the present invention is not particularly limited, but is preferably 0.01% by weight or more.

本発明化粧料中のフェノキシエタノールの含有量として
は特に限定されないが、皮膚安全性及び防腐防黴効果の
点から、0.O1〜2.0重量%の範囲が好ましい。
The content of phenoxyethanol in the cosmetics of the present invention is not particularly limited, but from the viewpoint of skin safety and antiseptic and antifungal effects, the content is 0. A range of 1 to 2.0% by weight of O is preferred.

本発明化粧料の剤型としては特に限定されず、例えば液
状、乳液状、クリーム状等の皮膚化粧料、メーキャップ
化粧料、毛髪化粧料、パック料等の各種化粧料剤型が挙
げられるが、水を含有する化粧料、特に水を1重量%以
上含有するものが好ましい。また、化粧料のpHは、7
.0以上、特に7.0〜9.0であることが好ましい。
The dosage form of the cosmetic of the present invention is not particularly limited, and examples thereof include various cosmetic dosage forms such as liquid, milky lotion, cream, etc., skin cosmetics, makeup cosmetics, hair cosmetics, packs, etc. Cosmetics containing water, particularly those containing 1% by weight or more of water, are preferred. In addition, the pH of cosmetics is 7.
.. It is preferably 0 or more, particularly 7.0 to 9.0.

また、本発明化粧料には、更に油剤、界面活性剤、水溶
性高分子、顔料、香料、紫外線吸収剤、酸化防止剤、ア
ルコール類、美肌用成分等、通常の化粧料に用いられる
成分を配合することができる。なお、必要であれば従来
使用されている防腐防黴剤を本発明の効果を損なわない
範囲で併用してもよい。
In addition, the cosmetics of the present invention further contain ingredients used in ordinary cosmetics, such as oils, surfactants, water-soluble polymers, pigments, fragrances, ultraviolet absorbers, antioxidants, alcohols, and skin-beautifying ingredients. Can be blended. Incidentally, if necessary, a conventionally used preservative and fungicide may be used in combination without impairing the effects of the present invention.

[実施例] 以下、実施例を挙げてさらに詳細に説明するが、本発明
はこれらに限定されるものではない。
[Examples] Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited thereto.

実施例1及び比較例1〜5 クリーム(pH約8.5) 表1に示す処方のクリームを常法に従って調製し、下記
のごとくして防腐効果及び経時安定性について試験を行
なった。
Example 1 and Comparative Examples 1 to 5 Cream (pH approximately 8.5) Creams having the formulations shown in Table 1 were prepared according to conventional methods, and tested for antiseptic effect and stability over time as described below.

(防腐試験) 前培養した供試菌(黴:1株、酵母:3株、細菌=3株
)各々を、10’cells/gとなるように実施例1
及び比較例1〜5のクリームに接種し、経時的に生菌数
を調べ、次の基準を全て満たすものを01少なくとも一
つを満たさないものを×とした。
(Preservation test) Each of the pre-cultured test bacteria (mold: 1 strain, yeast: 3 strains, bacteria = 3 strains) was prepared in Example 1 at a concentration of 10'cells/g.
The creams of Comparative Examples 1 to 5 were inoculated, and the number of viable bacteria was checked over time. Those that met all of the following criteria were rated 0, and those that did not meet at least one were rated x.

黴 :4週間後の生菌数が10’cells/g未満酵
母:4週間後の生菌数がIO’cells/g未満細菌
=2週間後の生菌数が10”calls/g未満(経時
安定性試験) 実施例1及び比較例1〜5のクリームを40℃の恒温槽
中にて1力月間放置後、目視により観察して、変化なし
を○、結晶析出等の変化ありを×とした。
Mold: The number of viable bacteria after 4 weeks is less than 10'cells/g Yeast: The number of viable bacteria after 4 weeks is less than IO'cells/g Bacteria = The number of viable bacteria after 2 weeks is less than 10'calls/g (over time) Stability test) The creams of Example 1 and Comparative Examples 1 to 5 were left in a constant temperature bath at 40°C for one month and then visually observed. No change was marked as ○, and changes such as crystal precipitation were marked as ×. did.

これらの結果を表1に示す。These results are shown in Table 1.

(以下余白) 表1 実施例2 乳液(pH約82) (成分)              (重量%)(1
)スクワラン             30(2)ホ
ホバ浦              20(3)ジメチ
ルポリシロキサン(1oocs)    0.5(4)
セタノール              0.5(5)
ベヘニルアルコール         05(6)モノ
ステアリン酸グリセリン     1.0(7)モノス
テアリン酸ポリエチレン グリコール(40E、0.)           0
.5(8)ビタミンEアセテート        0.
05(9)L−アスコルビン酸−2−リン酸マグネシウ
ム塩            30(10)クエン酸ナ
トリウム         1.0(11)キサンタン
ガム           0.2(12)エラスチン
加水分解物       0.1(1303−ブチレン
グリコール       90〈14)フェノキシエタ
ノール        0.3(15)桔製氷    
          残量上記各成分を用い、常法に従
って乳液を製造し、実施例1と同様にして防腐効果及び
経時安定性を評価したところ、いずれも満足できるもの
であった。
(Margins below) Table 1 Example 2 Emulsion (pH approx. 82) (Ingredients) (Weight %) (1
) Squalane 30 (2) Jojobaura 20 (3) Dimethylpolysiloxane (1oocs) 0.5 (4)
Setanol 0.5 (5)
Behenyl alcohol 05 (6) Glyceryl monostearate 1.0 (7) Polyethylene glycol monostearate (40E, 0.) 0
.. 5(8) Vitamin E acetate 0.
05 (9) L-ascorbic acid-2-phosphate magnesium salt 30 (10) Sodium citrate 1.0 (11) Xanthan gum 0.2 (12) Elastin hydrolyzate 0.1 (1303-butylene glycol 90 <14 ) Phenoxyethanol 0.3 (15) Kisei Ice
A milky lotion was prepared according to a conventional method using the remaining amounts of each of the above components, and the preservative effect and stability over time were evaluated in the same manner as in Example 1, and both results were satisfactory.

実施例3 化粧液(pH約8.3) (成分)               (重量%)(
1)ホホバ油              01(2)
ポリオキシエチレン 硬化ヒマシ油(60E、0.)          1
.0(3)水素添加大豆リン脂質        0.
1(4)エス力ロール507(ヴアンダイク社製)O2
(5)L−アスコルビン酸−2−リン酸マグネシウム塩 (6)人参エキス (7)キサンタンガム (8)マルメロ抽出液 (9)リン酸二水素カリウム (10)リン酸水素二ナトリウム (11)水酸化ナトリウム (120,3−ブチレングリコール (13)グリセリン 5 1 O02 20口 0.01 5 0.04 5.0 0 (14)フェノキシエタノール        05(
15)稍製水               残量上記
各成分を用い、常法に従って化粧液を製造し、実施例1
と同様にして防腐効果及び経時安定性を評価したところ
、いずれも満足できるものであった。
Example 3 Cosmetics (pH approx. 8.3) (Ingredients) (Weight %) (
1) Jojoba oil 01(2)
Polyoxyethylene hydrogenated castor oil (60E, 0.) 1
.. 0(3) Hydrogenated soybean phospholipid 0.
1 (4) S-Riki Roll 507 (manufactured by Van Dyke) O2
(5) L-ascorbic acid-2-phosphate magnesium salt (6) Ginseng extract (7) Xanthan gum (8) Quince extract (9) Potassium dihydrogen phosphate (10) Disodium hydrogen phosphate (11) Hydroxylation Sodium (120,3-butylene glycol (13) Glycerin 5 1 O02 20 mouths 0.01 5 0.04 5.0 0 (14) Phenoxyethanol 05 (
15) Remaining amount of water made from pure water A cosmetic lotion was manufactured according to a conventional method using each of the above ingredients, and Example 1
When the preservative effect and stability over time were evaluated in the same manner as above, both were found to be satisfactory.

実施例4 化粧水CpH約80) (成分)               (重量%)(
2)セスキオレイン酸ソルビタン     0.05(
4)2−エチルへキサン酸トリグリセライド(5)エス
力ロール507(ヴアンダイク社製)4 1 (7)乳酸 (8)乳酸ナトリウム 0.01 0.2 (9)2−アミノ−2−メチル−13−プロパンジオー
ル 025 (lO)ハマメリス抽出エキス        0.1
(11)ソルビトール           0.1(
12)エタノール             5.0(
13)グリセリン             5.0(
14)フェノキシエタノール        0.3(
15)精製水               残量上記
各成分を用い、常法に従って化粧水を製造し、実施例1
と同様にして防腐効果及び経時安定性を評価したところ
、いずれも満足できるものであった。
Example 4 Lotion CpH approx. 80) (Ingredients) (Weight%) (
2) Sorbitan sesquioleate 0.05 (
4) 2-Ethylhexanoic acid triglyceride (5) S-Ryki Roll 507 (manufactured by Vandyke) 4 1 (7) Lactic acid (8) Sodium lactate 0.01 0.2 (9) 2-Amino-2-methyl-13 -Propanediol 025 (lO) Hamamelis extract 0.1
(11) Sorbitol 0.1 (
12) Ethanol 5.0 (
13) Glycerin 5.0 (
14) Phenoxyethanol 0.3 (
15) Purified water Remaining amount Using each of the above ingredients, a lotion was manufactured according to a conventional method, and Example 1
When the preservative effect and stability over time were evaluated in the same manner as above, both were found to be satisfactory.

[発明の効果] 以上のように、アスコルビン酸すン酸エステル含有化粧
籾においてフェノキシエタノールを防腐防黴剤として用
いることにより、アスコルビン酸リン酸エステルが安定
で、かつ防腐防黴効果に優れた化粧料が提供される。
[Effect of the invention] As described above, by using phenoxyethanol as a preservative and antifungal agent in cosmetic rice containing ascorbic acid phosphate, a cosmetic product in which the ascorbic acid phosphate ester is stable and has an excellent preservative and antifungal effect can be obtained. is provided.

以上that's all

Claims (1)

【特許請求の範囲】[Claims] (1)アスコルビン酸リン酸エステルまたはその塩及び
フェノキシエタノールを含有することを特徴とする化粧
料。
(1) A cosmetic containing ascorbic acid phosphate or a salt thereof and phenoxyethanol.
JP20070789A 1989-08-02 1989-08-02 Cosmetic Pending JPH0363208A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20070789A JPH0363208A (en) 1989-08-02 1989-08-02 Cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20070789A JPH0363208A (en) 1989-08-02 1989-08-02 Cosmetic

Publications (1)

Publication Number Publication Date
JPH0363208A true JPH0363208A (en) 1991-03-19

Family

ID=16428889

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20070789A Pending JPH0363208A (en) 1989-08-02 1989-08-02 Cosmetic

Country Status (1)

Country Link
JP (1) JPH0363208A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0853338A (en) * 1994-08-11 1996-02-27 Shiseido Co Ltd Dermal agent for external use
US5605694A (en) * 1994-01-31 1997-02-25 L'oreal Stabilized emulsion intended to moisturize the skin, and use thereof
JP2003063943A (en) * 2001-08-27 2003-03-05 Tsumura & Co External preparation for skin
JP2007308515A (en) * 2001-03-23 2007-11-29 Rohto Pharmaceut Co Ltd Integumentary composition containing ascorbic acid
JP2012030583A (en) * 2010-06-29 2012-02-16 Ricoh Co Ltd Liquid composition, recording method, and recorded matter

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5605694A (en) * 1994-01-31 1997-02-25 L'oreal Stabilized emulsion intended to moisturize the skin, and use thereof
JPH0853338A (en) * 1994-08-11 1996-02-27 Shiseido Co Ltd Dermal agent for external use
JP2007308515A (en) * 2001-03-23 2007-11-29 Rohto Pharmaceut Co Ltd Integumentary composition containing ascorbic acid
JP2003063943A (en) * 2001-08-27 2003-03-05 Tsumura & Co External preparation for skin
JP2012030583A (en) * 2010-06-29 2012-02-16 Ricoh Co Ltd Liquid composition, recording method, and recorded matter

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