JP3525593B2 - Aqueous nail polish - Google Patents

Aqueous nail polish

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Publication number
JP3525593B2
JP3525593B2 JP29742795A JP29742795A JP3525593B2 JP 3525593 B2 JP3525593 B2 JP 3525593B2 JP 29742795 A JP29742795 A JP 29742795A JP 29742795 A JP29742795 A JP 29742795A JP 3525593 B2 JP3525593 B2 JP 3525593B2
Authority
JP
Japan
Prior art keywords
water
nail polish
acrylate
methacrylate
acrylic
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.)
Expired - Lifetime
Application number
JP29742795A
Other languages
Japanese (ja)
Other versions
JPH0971511A (en
Inventor
篤 松下
力 松尾
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.)
Kose Corp
Original Assignee
Kose Corp
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Filing date
Publication date
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Priority to JP29742795A priority Critical patent/JP3525593B2/en
Publication of JPH0971511A publication Critical patent/JPH0971511A/en
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Publication of JP3525593B2 publication Critical patent/JP3525593B2/en
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Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 【0001】 【発明の属する技術分野】本発明は、水に不溶で且つア
ルカリ水に溶解する樹脂とアクリル系ポリマーエマルジ
ョンとを配合した水系美爪料に関する。 【0002】 【従来の技術】従来より、美爪料は爪先のメイク化粧料
として広く汎用されてきており、その剤型はトルエン、
酢酸エステル類を中心とした溶剤タイプのものが主流で
あった。しかしながら、近年の安全性指向の高まりに従
い、有機溶剤を使用しないタイプの美爪料、例えば水系
のもの(以下「水系美爪料」という)が検討されるよう
になってきた。水系美爪料の場合、従来の美爪料とは異
なり、硝化綿のような強固な皮膜を形成する成分が使用
できないため、溶剤タイプと同等の付着性、膜強度、光
沢といった塗膜性能を有する製品の開発が主体となって
きている。従来、水系美爪料の皮膜形成剤として使用さ
れてきたアクリル系ポリマーエマルジョンは単独では美
爪料として使用に耐え得る塗膜強度、付着性、光沢等の
塗膜性能を満たすことはできないため、塗膜性能を向上
させるためにポリマーエマルジョンのガラス転移温度
(Tg)、粒径、又は構造の異なる2種以上のポリマー
を組み合わせて使用したり、ポリマーエマルジョン自体
を多層構造にして塗膜性能を向上させる試みがなされて
きた。 【0003】 【発明が解決しようとする課題】しかしながら、従来の
ポリマーエマルジョンを組み合わせる方法は、ポリマー
エマルジョン同士の相溶性が良くないことから塗膜の白
化、塗膜強度の低下等の問題が生じるため組み合わせる
ことが可能なポリマーエマルジョン種が大幅に限定され
てしまう。また、ポリマーエマルジョンの粒径が異なる
ものを組み合わせた場合は、美爪料自体が白濁し、外観
上好ましくない。このように従来の方法には種々の問題
点があり、ポリマーエマルジョンを組み合わることによ
って、目標とする品質を得ることは困難であった。一
方、多層構造のポリマーエマルジョンを使用した場合
は、効果的な塗膜物性の改善が可能ではあるが本発明者
らが追試した限りにおいては、有機溶剤タイプの美爪料
と同等の塗膜性能を得るまでには至っていない。従っ
て、塗膜性能は使用される皮膜形成剤の機能によって決
まってしまい、塗膜に光沢、付着性、強度といった機能
を付加的に持たせることは困難であった。このため、塗
膜に光沢、付着性、強度といった塗膜性能を調節できる
配合技術の開発が望まれてきた。 【0004】 【課題を解決するための手段】上記実情に鑑み、本発明
者らは鋭意研究の結果、水に不溶で且つアルカリ水に溶
解する樹脂とアクリル系ポリマーエマルジョンとを配合
すると、系における両者の相溶性が良好でかつ水系美爪
料の塗膜性能を自由に調節することが可能であることを
見いだし、本発明の完成に至った。 【0005】即ち、本発明は、水に不溶で且つ0.1規
定のアルカリ水に0.1重量%以上溶解し得るカルボキ
シル基含有アクリル系樹脂0.05〜20重量%とアク
リル系ポリマーエマルジョン2〜60重量%(固形分換
算)とを配合した水系美爪料であって、前記カルボキシ
ル基含有アクリル系樹脂はアルカリ水で中和しこれに溶
解して配合したことを特徴とする水系美爪料である。 【0006】 【発明の実施の形態】以下、本発明の構成について説明
する。本発明に使用される、水に不溶で且つ 0.1規定
のアルカリ水溶液に0.1重量%以上溶解し得るカルボ
キシル基含有アクリル系樹脂は、アクリル酸及び/又は
メタクリル酸の重合体或はアクリル酸及び/又はメタク
リル酸と他のモノマーの共重合体である。この他のモノ
マーとしてはアクリル酸メチル、アクリル酸エチル、ア
クリル酸アミド、アクリル酸n-プロピル、アクリル酸n-
ブチル、アクリル酸イソブチル、アクリル酸オクチル、
アクリル酸2−エチルヘキシル、N,N−ジメチルアミ
ノエチルアクリレート、アクリロニトリル、メタクリル
酸エチル、メタクリル酸アミド、メタクリル酸n-プロピ
ル、メタクリル酸n-ブチル、メタクリル酸イソブチル、
メタクリル酸2−エチルヘキシル、メタクリル酸オクチ
ル、メタクリル酸ハイドロキシエチル、N,N−ジメチ
ルアミノエチルメタクリレート等が挙げられる。重合法
は公知の方法により行ことができるが、その際、スチレ
ン、酢酸ビニル等を共重合させても良い。市販品として
は、ジョンクリル68(ジョンソンポリマー(株)製)
や、F−75(星光化学工業(株)製)、ダーマクリル
−79(カネボウ・エヌエスシー(株)製)等が挙げら
れる。これらの水に不溶で且つアルカリ水に溶解する
ルボキシル基含有アクリル系樹脂は、必要に応じ、1種
又は2種以上を用いることができる。これら本発明の水
に不溶で且つアルカリ水に溶解するカルボキシル基含有
アクリル系樹脂の配合量は、効果の発現や使用性の点で
0.05〜20%、更に好ましくは0.1〜15%であ
る。 【0007】本発明に使用されるアクリル系ポリマーエ
マルジョンは、アクリル酸、メタクリル酸あるいはそれ
らのアルキルエステル又は誘導体の中の1種又は2種以
上から選択されるモノマーの共重合体である。これらの
モノマーとしてはアクリル酸、アクリル酸メチル、アク
リル酸エチル、アクリル酸アミド、アクリル酸n-プロピ
ル、アクリル酸n-ブチル、アクリル酸イソブチル、アク
リル酸オクチル、アクリル酸2−エチルヘキシル、N,
N−ジメチルアミノエチルアクリレート、アクリロニト
リル、メタクリル酸、メタクリル酸エチル、メタクリル
酸アミド、メタクリル酸n-プロピル、メタクリル酸n-ブ
チル、メタクリル酸イソブチル、メタクリル酸2−エチ
ルヘキシル、メタクリル酸オクチル、メタクリル酸ハイ
ドロキシエチル、N,N−ジメチルアミノエチルメタク
リレート等が挙げられる。また、これらのモノマーを共
重合させる際、スチレン、酢酸ビニル等を共重合させて
も良い。得られたポリマーの構造も1層状もしくは多層
状であってもかまわない。また、その製法は、前記モノ
マーの1種又は2種以上を常法に従って重合させ、反応
混合物に必要に応じて水を加えることにより行われる。
好ましくは、反応性乳化剤を使用したソープフリー重合
や、乳化剤を含まない水媒体不均一重合等の公知の手法
で重合させる無乳化剤重合等が挙げられる。市販品とし
ては、J775、J537(いずれもジョンソンポリマ
ー(株)製)や、ヨドゾール GH28、同GH41
(いずれもカネボウ・エヌエスシー(株)製)、ボンコ
ート9422、同40−418(いずれも大日本インキ
化学工業(株)製)、プライマルC−72、同GL−6
18(いずれもローム・アンド・ハース・ジャパン
(株)製)、ポリゾール AM−200、同AP−26
79、同AP−2683(いずれも昭和高分子(株)
製)等が挙げられる。これらのアクリル系ポリマーエマ
ルジョンは、必要に応じ、1種又は2種以上を用いるこ
とができる。 【0008】上記アクリル系ポリマーエマルジョンの配
合量は、皮膜形成能や使用性の点で、固形分換算で2〜
60%、更に好ましくは5〜40%である。 【0009】本発明の上記の水に不溶で且つアルカリ水
に溶解するカルボキシル基含有アクリル系樹脂を中和す
るために用いられる塩基としては、通常化粧料に用いら
れるものであれば、特に限定されるものではないが、例
えばトリメチルアミン、N,N’−テトラ(ω−ヒドロ
キシプロピルオキシエトキシ)エチレンジアミン、トリ
エチルアミンの3級アンモニア塩、アンモニア、トリエ
タノールアミン、水酸化ナトリウム等が挙げられる。中
でもアンモニアのような揮発性の塩基を用いると耐水性
が良好で好ましい。中和度には特に制限はないが、最終
pHが中性付近になるように中和するのが望ましい。
に不溶で且つアルカリ水に溶解する樹脂は、アルカリ水
で中和してこれに溶解した後、アクリル系ポリマーエマ
ルジョンと混合する。 【0010】本発明の水系美爪料中には上記必須成分以
外に顔料、色素あるいはその他の化粧料用粉体を配合す
ることができる。これらの粉体はそのまま使用しても差
しつかえないが、もちろん必要に応じて、油剤、界面活
性剤、シリコーン、フッ素化合物等で処理して配合して
も良い。また、必要に応じ、顔料分散用の界面活性剤、
成膜助剤、粘度調整剤(ゲル化剤)、水溶性高分子、防
腐剤、消泡剤、可塑剤、酸化防止剤、香料、紫外線吸収
剤、美容成分等を適宜配合することができる。 【0011】本発明の水系美爪料には、ネイルエナメ
ル、エナメルトップコート、エナメルベースコート等を
挙げることができる。 【0012】 【実施例】以下、実施例によって本発明の効果をさらに
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。 【0013】実施例1〜4及び比較例1〜2 水系美爪
料 表1に示す処方の水系美爪料を調製し、のびの良さ、化
粧持ち(剥がれにくさ、かけにくさ)、光沢及び系にお
ける樹脂及びポリマーエマルジョンの相溶性について下
記の方法により各評価を行った。その結果も併せて表1
に示す。 【0014】 【表1】 【0015】*1:シ゛ョンソンホ゜リマー(株)製シ゛ョ
ンクリル 68:スチレン−アクリル酸共重合体 *2:星光化学工業(株)製F-75:アクリル酸−メタクリル
酸メチル共重合体 *3:カネホ゛ウ エヌエスシー(株)製ヨト゛ソ゛ール GH
28:アクリル酸エチル−メタクリル酸メチル共重合体
(固形分45%) *4:カネホ゛ウ エヌエスシー(株)製ヨト゛ソ゛ール GH
41:スチレン−アクリル酸アルキル共重合体(固形分45
%) 【0016】(製法) 実施例1〜4及び比較例1〜2 A.成分(5)に成分(1)、(2)及び(12)を溶
解させる。 B.成分(8)をA.に均一に分散させる。 C.B及び成分(3)、(4)、(6)、(7)、
(9)〜(11)を混合、脱気し、容器に充填して製品
とする。 【0017】(評価方法及び判定基準) 1.官能評価 各試料について、専門パネル20名による使用テストを
行い、各試料をのびの良さ、化粧持ち(剥がれにくさ、
かけにくさ)、光沢について、(1)絶対評価基準を用
いて5段階に評価し、各試料ごとの評点の平均値を
(2)4段階評価基準を用いて評価した。 (1)絶対評価基準 5点:非常に良好 4点:良好 3点:普通 2点:やや不良 1点:不良 (2)4段階評価基準 ◎:4.0〜5.0点 ○:3.0〜4.0点未満 △:2.0〜3.0点未満 ×:1.0〜2.0点未満 【0018】2.相溶性評価 各試料につき、ガラス板上に、ドクターブレードにて4
ミル厚さの均一な塗膜を調製し、室温下で一昼夜放置し
て充分風乾させた後、塗膜の透明性を肉眼にて評価し
た。 判定基準 ◎:透明 ○:やや白濁 △:白濁 ×:白濁し、塗膜の均一性がない 【0019】上記結果から明らかなように、本発明品に
係わる実施例1〜4の水系美爪料はのびの良さ、化粧持
ち(剥がれにくさ、かけにくさ)、光沢、相溶性といっ
た全ての点で、はるかに優れた特性を有していることが
わかる。これに対し、比較例の水系美爪料は、特に化粧
持ちの点で満足するものではなかった。 【0020】 実施例5 水系トップコート (成分) (%) 1.樹脂A *1 0.1 2.アクリル系ポリマーエマルジョンC *3 90.0 3.精製水 残量 4.中和剤 適量 5.カルビトール 2.5 6.可塑剤 適量 7.防腐剤 適量 8.消泡剤 適量 9.香料 適量 (製法) A.成分(1)を成分(3)及び(4)にて溶解させ
る。 B.Aと成分(2)、(5)〜(9)を均一になるまで
撹拌混合し、脱気し、容器に充填して製品とする。 【0021】本発明の水系トップコートは、使用性に優
れ、特にトップコートとしての機能である透明性(相溶
性が良い)、化粧持ちである膜強度及び付着性に優れた
ものであった。 【0022】 【発明の効果】本発明の水系美爪料は、のびの良さ等の
使用性に優れ、系における樹脂及びポリマーエマルジョ
ンの相溶性が良好で、光沢、付着性、強度といった塗膜
性能を必要に応じて調節することのできる優れたもので
あった。
BACKGROUND OF THE INVENTION [0001] [Technical Field of the Invention The present invention relates to water Keibi Tsumeryo compounded with a resin and an acrylic polymer emulsion that dissolves and the alkaline water is insoluble in water. 2. Description of the Related Art Conventionally, beauty nail preparations have been widely used as makeup cosmetics for toes, and their dosage forms are toluene,
Solvent-type solvents, mainly acetic esters, were the mainstream. However, with an increase in safety orientation in recent years, nail polish that does not use an organic solvent, for example, a water-based nail polish (hereinafter referred to as “aqueous nail polish”) has been studied. In the case of water-based nail pills, unlike conventional nail pills, components that form a strong film such as nitrified cotton cannot be used. The development of products that have it has become the main subject. Conventionally, acrylic polymer emulsions that have been used as film-forming agents for water-based nail polishes alone cannot satisfy coating properties such as coating strength, adhesion, and gloss that can withstand use as nail polishes. Use two or more polymers with different glass transition temperatures (Tg), particle sizes, or structures in combination to improve the coating performance, or improve the coating performance by using a multilayered polymer emulsion itself Attempts have been made to do so. [0003] However, the conventional method of combining polymer emulsions causes problems such as whitening of the coating film and reduction in the strength of the coating film due to poor compatibility between the polymer emulsions. The types of polymer emulsions that can be combined are greatly limited. Further, when polymer emulsions having different particle diameters are combined, the nail polish itself becomes cloudy, which is not preferable in appearance. As described above, the conventional methods have various problems, and it has been difficult to obtain a target quality by combining a polymer emulsion. On the other hand, when a polymer emulsion having a multilayer structure is used, it is possible to effectively improve the properties of the coating film. However, as far as the present inventors have carried out additional tests, the coating film performance is equivalent to that of the organic solvent type nail polish. Has not yet been obtained. Therefore, the performance of the coating film is determined by the function of the film forming agent used, and it has been difficult to give the coating film additional functions such as gloss, adhesion, and strength. For this reason, there has been a demand for the development of a compounding technique capable of adjusting the coating film performance such as gloss, adhesion and strength. [0004] In view of the above-mentioned circumstances, the present inventors have made intensive studies and found that, when a resin insoluble in water and soluble in alkaline water and an acrylic polymer emulsion are blended, an acrylic polymer emulsion is obtained. The inventors have found that the compatibility between the two is good and that the coating properties of the water-based nail polishes can be freely adjusted, and the present invention has been completed. [0005] That is, the present invention relates to a water-insoluble and 0.1 g
0.1% by weight or more soluble in fixed alkaline water
0.05 to 20% by weight of acrylic resin containing sil group
2-60% by weight of a ril-based polymer emulsion (solid content
And a water-based nail enamel containing the above carboxy.
Acrylic resin containing hydroxyl group is neutralized with alkaline water and dissolved in
It is a water-based beautiful nail material characterized by being disassembled and blended. [0006] The configuration of the present invention will be described below. As used in the present invention, and 0.1N insoluble in water
That can dissolve at least 0.1% by weight in an alkaline aqueous solution of
The xyl group-containing acrylic resin is acrylic acid and / or
Methacrylic acid polymer or acrylic acid and / or methacrylic acid
It is a copolymer of lylic acid and other monomers. Other monomers include methyl acrylate, ethyl acrylate, acrylamide, n-propyl acrylate, and n-acrylate.
Butyl, isobutyl acrylate, octyl acrylate,
2-ethylhexyl acrylate, N, N-dimethylaminoethyl acrylate, acrylonitrile, ethyl methacrylate, methacrylamide, n-propyl methacrylate, n-butyl methacrylate, isobutyl methacrylate,
Examples thereof include 2-ethylhexyl methacrylate, octyl methacrylate, hydroxyethyl methacrylate, and N, N-dimethylaminoethyl methacrylate. The polymerization method can be carried out by a known method, and in that case, styrene, vinyl acetate or the like may be copolymerized. As a commercially available product, John Krill 68 (manufactured by Johnson Polymer Co., Ltd.)
And F-75 (manufactured by Seiko Chemical Co., Ltd.), Dermacril-79 (manufactured by Kanebo NS Co., Ltd.), and the like. Ca that dissolves and the alkaline water is insoluble in these water
As the ruboxyl group-containing acrylic resin, if necessary, one or more kinds can be used. These carboxyl group- insoluble and water-soluble carboxyl groups of the present invention
The amount of the acrylic resin is from 0.05 to 20 percent in terms of expression and use of effects, more preferably from 0.1% to 15%. [0007] The acrylic polymer emulsion used in the present invention is a copolymer of a monomer selected from one or more of acrylic acid, methacrylic acid or their alkyl esters or derivatives. These monomers include acrylic acid, methyl acrylate, ethyl acrylate, acrylamide, n-propyl acrylate, n-butyl acrylate, isobutyl acrylate, octyl acrylate, 2-ethylhexyl acrylate, N,
N-dimethylaminoethyl acrylate, acrylonitrile, methacrylic acid, ethyl methacrylate, methacrylamide, n-propyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, 2-ethylhexyl methacrylate, octyl methacrylate, hydroxyethyl methacrylate , N, N-dimethylaminoethyl methacrylate and the like. When these monomers are copolymerized, styrene, vinyl acetate and the like may be copolymerized. The structure of the obtained polymer may be a single layer or a multilayer. In addition, the production method is carried out by polymerizing one or more of the above monomers in accordance with a conventional method, and adding water to the reaction mixture as needed.
Preferably, emulsifier-free polymerization in which polymerization is carried out by a known method such as soap-free polymerization using a reactive emulsifier, heterogeneous polymerization in an aqueous medium containing no emulsifier, and the like. Commercially available products include J775 and J537 (both manufactured by Johnson Polymer Co., Ltd.), Iodozol GH28 and GH41
(All manufactured by Kanebo NS Co., Ltd.), Boncoat 9422 and 40-418 (all manufactured by Dainippon Ink and Chemicals, Inc.), Primal C-72, and GL-6
18 (all manufactured by Rohm and Haas Japan KK), Polysol AM-200, AP-26
79, AP-2683 (both are Showa High Polymer Co., Ltd.)
Manufactured). One or more of these acrylic polymer emulsions can be used as needed. [0008] The amount of the acrylic polymer emulsion, in terms of peel film forming ability and usability, 2 on a solid basis
It is 60%, more preferably 5 to 40%. [0009] As the base used to and neutralizing the carboxyl group-containing acrylic resin which is soluble in alkaline water insoluble to the water of the present invention, as long as it is usually used in cosmetics, particularly limited Although not limited thereto, for example, trimethylamine, N, N′-tetra (ω-hydroxypropyloxyethoxy) ethylenediamine, a tertiary ammonia salt of triethylamine, ammonia, triethanolamine, sodium hydroxide and the like can be mentioned. Among them, the use of a volatile base such as ammonia is preferable because of good water resistance. Although there is no particular limitation on the degree of neutralization, it is desirable to neutralize so that the final pH is near neutrality. water
Resins that are insoluble in water and soluble in alkaline water
Neutralize with and dissolve in this
Mix with Rejon. [0010] In addition to the above essential components, pigments, pigments or other cosmetic powders can be incorporated into the aqueous nail polishes of the present invention. These powders may be used as they are, but of course, if necessary, may be treated with an oil agent, a surfactant, silicone, a fluorine compound, or the like and blended. Also, if necessary, a surfactant for pigment dispersion,
A film forming aid, a viscosity modifier (gelling agent), a water-soluble polymer, a preservative, an antifoaming agent, a plasticizer, an antioxidant, a fragrance, an ultraviolet absorber, a cosmetic ingredient, and the like can be appropriately compounded. The nail polish of the present invention includes nail enamel, enamel top coat, enamel base coat and the like. EXAMPLES Hereinafter, the effects of the present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples. Examples 1 to 4 and Comparative Examples 1 to 2 Aqueous nail polish A water-based nail polish having the formulation shown in Table 1 was prepared, and had good spreadability, long-lasting makeup (difficulty in peeling and hard to apply), gloss and gloss. The compatibility of the resin and the polymer emulsion in the system was evaluated by the following methods. Table 1 also shows the results.
Shown in [Table 1] * 1: Shonsoncryl Co., Ltd. manufactured by Shonson Polymer Co., Ltd. 68: Styrene-acrylic acid copolymer * 2: F-75: Shikotsu Chemical Co., Ltd .: Acrylic acid-methyl methacrylate copolymer * 3: Kanehou NS Corporation YOTO SOUL GH
28: Ethyl acrylate-methyl methacrylate copolymer
(Solid content: 45%) * 4: Yodosol GH manufactured by Kanebo NSC Co., Ltd.
41: Styrene- alkyl acrylate copolymer (solid content 45
(Production method) Examples 1-4 and Comparative Examples 1-2 A. The components (1), (2) and (12) are dissolved in the component (5). B. Component (8) Disperse evenly. C. B and components (3), (4), (6), (7),
(9) to (11) are mixed, degassed, and filled in a container to obtain a product. (Evaluation Method and Judgment Criteria) For each sensory evaluation sample, a use test was conducted by 20 specialized panels, and each sample was evaluated for good spreadability, long-lasting makeup (hard to peel,
(1) Five-step evaluation using absolute evaluation criteria, and (2) four-step evaluation criteria for average value of each sample. (1) Absolute evaluation criterion 5 points: Very good 4 points: Good 3 points: Normal 2 points: Slightly poor 1 point: Poor (2) Four-step evaluation criteria :: 4.0 to 5.0 points :: 3. 0 to less than 4.0 points: 2.0 to less than 3.0 points x: 1.0 to less than 2.0 points Compatibility evaluation For each sample, put 4 pieces on a glass plate with a doctor blade.
After preparing a uniform coating film having a mill thickness and allowing it to stand at room temperature for 24 hours to air-dry sufficiently, the transparency of the coating film was visually evaluated. Criteria :: transparent ○: slightly cloudy Δ: cloudy ×: cloudy and no uniformity of the coating film As is apparent from the above results, the aqueous nail polishes of Examples 1-4 according to the present invention. It can be seen that it has much better properties in all respects such as good spreadability, long-lasting makeup (hard to peel and hard to spread), gloss and compatibility. On the other hand, the water-based nail polish of Comparative Example was not particularly satisfactory in terms of long-lasting makeup. Example 5 Aqueous Topcoat (Component) (%) Resin A * 1 0.1 2. 2. Acrylic polymer emulsion C * 3 90.0 Purified water balance 4. Neutralizer appropriate amount5. Carbitol 2.5 6. Plasticizer appropriate amount 7. Preservative qs 8. Defoamer appropriate amount 9. Appropriate amount of fragrance (production method) A. Component (1) is dissolved in components (3) and (4). B. A and components (2) and (5) to (9) are stirred and mixed until uniform, degassed, and filled into a container to obtain a product. The water-based topcoat of the present invention was excellent in usability, and in particular, was excellent in transparency (good compatibility), which is a function as a topcoat, and in film strength and adhesion for long-lasting makeup. The water-based nail polish of the present invention has excellent usability such as good spreadability, good compatibility of resin and polymer emulsion in the system, and coating properties such as gloss, adhesion and strength. Was an excellent one that could be adjusted as needed.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 平4−103513(JP,A) 特開 平3−133916(JP,A) 特開 平5−32821(JP,A) (58)調査した分野(Int.Cl.7,DB名) A61K 7/00 - 7/50 CA(STN)────────────────────────────────────────────────── ─── Continuation of the front page (56) References JP-A-4-103513 (JP, A) JP-A-3-133916 (JP, A) JP-A-5-32821 (JP, A) (58) Field (Int. Cl. 7 , DB name) A61K 7/ 00-7/50 CA (STN)

Claims (1)

(57)【特許請求の範囲】 【請求項1】水に不溶で且つ0.1規定のアルカリ水に
0.1重量%以上溶解し得るカルボキシル基含有アクリ
ル系樹脂0.05〜20重量%とアクリル系ポリマーエ
マルジョン2〜60重量%(固形分換算)とを配合した
水系美爪料であって、前記カルボキシル基含有アクリル
系樹脂はアルカリ水で中和しこれに溶解して配合した
とを特徴とする水系美爪料。
(57) [Claims] [Claim 1] Insoluble in water and in 0.1N alkaline water
0.1% by weight or more soluble carboxyl group-containing acrylic
0.05-20% by weight of acrylic resin and acrylic polymer
2 to 60% by weight (in terms of solid content)
A water-based beauty nail material, wherein the carboxyl group-containing acrylic
A water based nail polish characterized by that the resin is neutralized with alkaline water, dissolved in the water and blended .
JP29742795A 1995-06-30 1995-10-20 Aqueous nail polish Expired - Lifetime JP3525593B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP29742795A JP3525593B2 (en) 1995-06-30 1995-10-20 Aqueous nail polish

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP7-188187 1995-06-30
JP18818795 1995-06-30
JP29742795A JP3525593B2 (en) 1995-06-30 1995-10-20 Aqueous nail polish

Publications (2)

Publication Number Publication Date
JPH0971511A JPH0971511A (en) 1997-03-18
JP3525593B2 true JP3525593B2 (en) 2004-05-10

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ID=26504771

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Country Status (1)

Country Link
JP (1) JP3525593B2 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4156697B2 (en) * 1997-11-27 2008-09-24 三菱化学株式会社 Water-based beauty nail
WO2002043676A1 (en) * 2000-11-29 2002-06-06 Shiseido Company, Ltd. Nail-care products
JP2003171220A (en) * 2001-12-07 2003-06-17 Nippon Junyaku Kk Cosmetic, binder for cosmetic and method for producing the same
JP3738439B2 (en) * 2001-12-07 2006-01-25 日本純薬株式会社 Manufacturing method of nail polish binder, nail polish binder and nail polish
JP5574971B2 (en) * 2008-11-11 2014-08-20 三菱鉛筆株式会社 Water-based nail polish and applicator with built-in nail polish
JP5669399B2 (en) * 2010-01-07 2015-02-12 三菱鉛筆株式会社 Aqueous cosmetics
WO2011083679A1 (en) * 2010-01-06 2011-07-14 三菱鉛筆株式会社 Aqueous cosmetic preparation
JP5669398B2 (en) * 2010-01-06 2015-02-12 三菱鉛筆株式会社 Aqueous cosmetics

Also Published As

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