JPH08143427A - Manicure - Google Patents

Manicure

Info

Publication number
JPH08143427A
JPH08143427A JP6314163A JP31416394A JPH08143427A JP H08143427 A JPH08143427 A JP H08143427A JP 6314163 A JP6314163 A JP 6314163A JP 31416394 A JP31416394 A JP 31416394A JP H08143427 A JPH08143427 A JP H08143427A
Authority
JP
Japan
Prior art keywords
resin
nail
acrylic
silicone
sulfonamide
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.)
Granted
Application number
JP6314163A
Other languages
Japanese (ja)
Other versions
JP3486826B2 (en
Inventor
Toshiyuki Ito
利之 伊藤
Kazuhiro Ishida
一弘 石田
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.)
Kose Corp
Original Assignee
Kose Corp
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 Kose Corp filed Critical Kose Corp
Priority to JP31416394A priority Critical patent/JP3486826B2/en
Publication of JPH08143427A publication Critical patent/JPH08143427A/en
Application granted granted Critical
Publication of JP3486826B2 publication Critical patent/JP3486826B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE: To obtain a manicure, excellent in color development, gloss and drying properties and good in makeup durability by blending a manicure comprising nitrocellulose, a plasticizer and a solvent with a silicone-based resin, an acrylic resin and/or a sulfonamide-based resin. CONSTITUTION: This manicure is obtained by blending nitrocellulose with a manicure containing nitrocellulose, a plasticizer and a solvent with a silicone- based resin, an acrylic resin and/or a sulfonamide-based resin. An acrylic- silicone-based graft copolymer is preferred as the silicone-based resin and, e.g. a compound of the formula (R1 is methyl or H; R2 is a 1-10C bivalent hydrocarbon) is preferred. A butyl acrylate-acrylonitrile-styrene copolymer is especially preferred as the acrylic resin and a toluenesulfonamide resin or a toluenesulfonamide epoxy resin is preferred as the sulfonamide-based resin. The manicure preferably contains 0.2-5wt.% silicone-based resin, 1-15wt.% acrylic resin and 1-25wt.% sulfonamide-based resin blended therein.

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、硝化綿、可塑剤、溶剤
を含有する美爪料において、シリコーン系樹脂及びアク
リル系樹脂及び/又はスルホンアミド系樹脂を配合し、
発色、艶、乾燥性に優れ、化粧持ちの良い美爪料に関す
る。
TECHNICAL FIELD The present invention relates to a nail varnish containing nitrification cotton, a plasticizer, and a solvent, in which a silicone resin and an acrylic resin and / or a sulfonamide resin are blended,
The present invention relates to a nail enamel that has excellent color development, luster and dryness and has a long-lasting makeup.

【0002】[0002]

【従来の技術】従来、美爪料に求められる品質として塗
膜の乾燥性、艶、発色、化粧持ちなどが挙げられる。塗
布膜の艶を向上させる技術としては、スルホンアミド系
樹脂や、アルキッド樹脂を配合することなどが知られて
いる。塗布膜の発色を向上させる技術としては、顔料の
チップ化による分散性の向上や、硫酸バリウムを配合す
ることなどが知られている。化粧もちを向上させる技術
としては、スルホンアミド系樹脂、シュークローズベン
ゾエート等を配合すること(特開昭60−21560
7)等が知られている。最近では、塗膜の速乾性に関心
が集まっており、速乾性の美爪料や速乾スプレー等が多
く発売されている。
2. Description of the Related Art Conventionally, the qualities required of nail enamel include the drying property of a coating film, luster, color development, and makeup retention. As a technique for improving the gloss of the coating film, it is known to blend a sulfonamide resin or an alkyd resin. Known techniques for improving the color development of the coating film include improving the dispersibility by chipping the pigment and blending barium sulfate. As a technique for improving makeup lasting, a sulfonamide-based resin, sucrose benzoate or the like may be blended (Japanese Patent Laid-Open No. 60-21560).
7) etc. are known. Recently, attention has been focused on the quick-drying property of a coating film, and many quick-drying nail polishes and quick-drying sprays have been released.

【0003】[0003]

【発明が解決しようとする課題】速乾性のスプレーは、
揮発性溶剤による樹脂からの溶剤の溶剤離れ促進効果に
より速乾性を演出しているが、その効果は充分なものと
は言えず、更に美爪料を塗布した後、これを噴霧する必
要があり使用性に煩雑さがあるという欠点があった。
又、速乾性の美爪料については、その効果を演出するた
めに溶剤組成を変えたり、樹脂濃度を低くしたり、シリ
コーン誘導体等を配合することがなされているが(特開
平2ー25411)、溶剤組成の調整だけでは充分な効
果は得られず、系の安定性を損ねるという欠点があっ
た。又、樹脂濃度を低くすると、塗布膜が薄くなってし
まい、化粧もちが悪くなるという欠点があった。シリコ
ーン誘導体を美爪料に配合した場合、シリコーン誘導体
は他の樹脂との相溶性が悪く、爪への付着性が悪いた
め、経時で塗布膜が部分的に剥がれてしまったり、爪先
端部から削れてくるなどの化粧持ちが悪くなってしまう
という欠点があった。上記の欠点を改良する方法とし
て、様々な樹脂の配合が検討がなされてきたが、いまだ
充分といえる効果は得られていなかった。すなわち、美
爪料において塗膜の乾燥性に優れ、かつ化粧持ちをさら
に向上させることが望まれていた。
[Problems to be Solved by the Invention] A quick-drying spray is
The volatile solvent has an effect of promoting solvent separation from the resin to produce quick drying, but the effect is not sufficient, and it is necessary to spray this after applying nail enamel. There was a drawback that the usability was complicated.
Also, for quick-drying nail enamel, in order to exert its effect, the solvent composition is changed, the resin concentration is lowered, and a silicone derivative or the like is blended (JP-A-2-25411). However, a sufficient effect cannot be obtained only by adjusting the solvent composition, and there is a drawback that the stability of the system is impaired. Further, when the resin concentration is lowered, the coating film becomes thin, and the makeup lasts poorly. When a silicone derivative is mixed in a nail varnish, the silicone derivative has poor compatibility with other resins and poor adhesion to the nail, so the coating film may partly peel off over time, or from the tip of the nail. It had the drawback that the makeup lasted poorly, such as being worn away. As a method of improving the above-mentioned drawbacks, various resin formulations have been studied, but the sufficient effect has not been obtained yet. That is, it has been desired that the coating film of the nail enamel is excellent in dryness and that the makeup retention is further improved.

【0004】[0004]

【課題を解決するための手段】かかる実情に鑑み、本発
明者らは、鋭意研究を行った結果、硝化綿、可塑剤、溶
剤を含有する美爪料において、シリコーン系樹脂と、ア
クリル系樹脂及び/又はスルホンアミド系樹脂とを配合
することにより、シリコーン誘導体の相溶性が良くな
り、塗布膜の化粧持ちを向上させ、乾燥性、発色、艶に
優れた美爪料が得られることを見い出し本発明を完成さ
せた。すなわち、硝化綿、可塑剤、溶剤を含有する美爪
料において、本発明はシリコーン系樹脂とアクリル系樹
脂及び/又はスルホンアミド系樹脂を配合することを特
徴とする美爪料である。
In view of the above situation, the inventors of the present invention have conducted earnest research, and as a result, in a nail varnish containing nitrification cotton, a plasticizer, and a solvent, a silicone resin and an acrylic resin were used. It has been found that, by blending with and / or a sulfonamide resin, the compatibility of the silicone derivative is improved, the makeup retention of the coating film is improved, and a nail enamel excellent in drying property, color development and luster is obtained. The present invention has been completed. That is, in the nail enamel containing nitrified cotton, a plasticizer, and a solvent, the present invention is a nail enamel characterized by blending a silicone resin and an acrylic resin and / or a sulfonamide resin.

【0005】本発明に用いられるシリコーン系樹脂は、
通常化粧料に用いられるものを使用する事ができる。
The silicone resin used in the present invention is
The thing normally used for cosmetics can be used.

【0006】好ましくは、アクリル−シリコーン系グラ
フト共重合体が挙げられる。アクリル−シリコーン系グ
ラフト共重合体は、特開平2−25411号公報等に記
載されているものが例示され、例えば、一般式(1)で
示される、分子鎖の片末端にラジカル重合性基を有する
ジメチルポリシロキサン化合物(A)と、アクリレート
及び/又はメタクリレートを主体とするラジカル重合性
モノマー(B)とをラジカル共重合させることにより合
成されるものである。
Preferably, an acrylic-silicone graft copolymer is used. Examples of the acrylic-silicone-based graft copolymer include those described in JP-A-2-25411 and the like. For example, a radical polymerizable group at one end of the molecular chain represented by the general formula (1) is used. It is synthesized by radically copolymerizing the dimethylpolysiloxane compound (A) and the radically polymerizable monomer (B) mainly containing acrylate and / or methacrylate.

【0007】[0007]

【化1】 Embedded image

【0008】R1:メチル基または水素原子 R2:場合によりエーテル結合一個または二個で遮断さ
れている直鎖状または分岐鎖状の炭素鎖を有する炭素原
子1〜10個の二価の飽和炭化水素基を示し、具体的に
は、−CH2−、−(CH23−、−(CH26−、−
(CH28−、−(CH210−、−CH2CH(C
3)CH2−、−(CH22O(CH23−、−(CH
22OCH2CH(CH3)CH2−、−(CH2CH
2O)2(CH23−等が例示される。 n:3〜300
R 1 is a methyl group or a hydrogen atom R 2 is a divalent saturated carbon atom having 1 to 10 carbon atoms having a linear or branched carbon chain optionally blocked by one or two ether bonds. a hydrocarbon group, specifically, -CH 2 -, - (CH 2) 3 -, - (CH 2) 6 -, -
(CH 2) 8 -, - (CH 2) 10 -, - CH 2 CH (C
H 3) CH 2 -, - (CH 2) 2 O (CH 2) 3 -, - (CH
2) 2 OCH 2 CH (CH 3) CH 2 -, - (CH 2 CH
2 O) 2 (CH 2 ) 3 — and the like are exemplified. n: 3 to 300

【0009】一方、(B)のアクリレート及び/又はメ
タクリレートを主体とするラジカル重合性モノマーは、
ラジカル重合性不飽和結合を分子中に一個有する化合物
を意味し、使用されるアクリレート及び/又はメタクリ
レートとしては、メチル(メタ)アクリレート、エチル
(メタ)アクリレート、n−ブチル(メタ)アクリレー
ト、2−エチルヘキシル(メタ)アクリレート等のアル
キル(メタ)アクリレート、2−ヒドロキシエチル(メ
タ)アクリレート、2−ヒドロキシプロピル(メタ)ア
クリレート等のヒドロキシアルキル(メタ)アクリレー
ト、フルオロ炭素鎖1〜10のパーフロロアルキル(メ
タ)アクリレート等を例示することができる。
On the other hand, the radically polymerizable monomer (B) mainly composed of acrylate and / or methacrylate is
It means a compound having one radical-polymerizable unsaturated bond in the molecule, and as the acrylate and / or methacrylate used, methyl (meth) acrylate, ethyl (meth) acrylate, n-butyl (meth) acrylate, 2- Alkyl (meth) acrylates such as ethylhexyl (meth) acrylate, hydroxyalkyl (meth) acrylates such as 2-hydroxyethyl (meth) acrylate and 2-hydroxypropyl (meth) acrylate, perfluoroalkyl of fluorocarbon chains 1-10 ( Examples thereof include (meth) acrylate.

【0010】本発明におけるラジカル重合性モノマーに
おいて上記したアクリレート及び/又はメタクリレート
以外に必要に応じて種々の化合物を使用することができ
る。これらの重合性モノマーとしては、スチレン、置換
スチレン、酢酸ビニル、(メタ)アクリル酸、無水マレ
イン酸、マレイン酸エステル、フマル酸エステル、塩化
ビニル、塩化ビニリデン、エチレン、プロピレン、ブタ
ジエン、アクリロニトリル、フッ化オレフィン等を例示
することができる。
In the radical-polymerizable monomer in the present invention, various compounds other than the above-mentioned acrylate and / or methacrylate can be used if necessary. These polymerizable monomers include styrene, substituted styrene, vinyl acetate, (meth) acrylic acid, maleic anhydride, maleic acid ester, fumaric acid ester, vinyl chloride, vinylidene chloride, ethylene, propylene, butadiene, acrylonitrile, fluorinated An olefin etc. can be illustrated.

【0011】シリコーン系樹脂の配合量は、0.2〜5
重量%(以下単に「%」で示す)が好ましい。更に、
0.5〜3%がより好ましく、塗膜の乾燥性がより向上
する。
The blending amount of the silicone resin is 0.2-5.
Weight percent (hereinafter simply referred to as "%") is preferred. Furthermore,
0.5 to 3% is more preferable, and the drying property of the coating film is further improved.

【0012】本発明で用いられるアクリル系樹脂は、
(メタ)アクリル酸誘導体を構成モノマーとしてもつも
のであれば特に限定されなく、アクリル酸ブチルアクリ
ル酸エチル共重合体(市販品としては、松本製薬工業社
製のオリゲンE等)、アクリル酸エチルメタクリル酸エ
チル共重合体(市販品としては、大東化成社製のダイト
ゾール5000AP等)、アクリル酸オクチルスチレン
共重合体等が例示されるが、なかでも構成モノマーに、
アクリル酸誘導体とスチレン及び/又はアクリロニトリ
ルをもつ、化合物が好ましく、特にアクリル酸ブチルア
クリロニトリルスチレン共重合体(市販品としては、ポ
リビニルケミカル社製のネオクリルB−1000等)が
より好ましい。
The acrylic resin used in the present invention is
It is not particularly limited as long as it has a (meth) acrylic acid derivative as a constituent monomer, and is not limited to butyl acrylate ethyl acrylate copolymer (commercially available product is ORIGEN E manufactured by Matsumoto Pharmaceutical Co., Ltd.), ethyl acrylate methacrylate. Ethyl acid copolymer (as a commercial product, Daito Kasei Co., Ltd. Daitozol 5000AP, etc.), octyl styrene acrylate copolymer, etc. are exemplified, but among them, the constituent monomers are
A compound having an acrylic acid derivative and styrene and / or acrylonitrile is preferable, and a butyl acrylonitrile styrene copolymer acrylate (as a commercial product, Neocryl B-1000 manufactured by Polyvinyl Chemical Co., Ltd.) is more preferable.

【0013】アクリル系樹脂の配合量は、化粧もち向上
の効果の点では1〜15%が好ましい。更に好ましく
は、2〜10%でより効果を発揮する。
The amount of the acrylic resin compounded is preferably 1 to 15% from the viewpoint of the effect of improving makeup lasting. More preferably, 2 to 10% is more effective.

【0014】本発明で用いられるスルホンアミド系樹脂
は、スルホンアミド基を有する樹脂であれば特に制限さ
れなく、トルエンスルホンアミドエポキシ樹脂(市販品
としては、エストロンケミカル社製のPolytex
E−100、テレケミテ社製のNAGELLITE30
50等)等が例示されるが、特に、トルエンスルホンア
ミド樹脂(市販品としては、モンサント社製のサントラ
イト等)が好ましい。
The sulfonamide resin used in the present invention is not particularly limited as long as it is a resin having a sulfonamide group. Toluene sulfonamide epoxy resin (commercially available product is Polytex manufactured by Estron Chemical Co., Ltd.).
E-100, NAGELLITE 30 manufactured by Telechemite
50 etc.) and the like, but toluenesulfonamide resin (as a commercial product, Santolite manufactured by Monsanto Co., Ltd.) is particularly preferable.

【0015】スルホンアミド系樹脂の配合量は、1〜2
5%が好ましい。更に、5〜15%であれば、化粧もち
向上の点ではより効果を発揮する。
The blending amount of the sulfonamide resin is 1 to 2
5% is preferable. Further, if it is 5 to 15%, it is more effective in improving makeup lasting.

【0016】本発明の美爪料は、上記の必須成分に加え
必要に応じて本発明の効果を損なわない程度に通常化粧
料に用いられる樹脂、可塑剤、粉体(顔料、染料、パー
ル剤等)、有機変性ベントナイト、溶剤、水性成分、油
性成分、紫外線吸収剤等を配合する事ができる。本発明
の美爪料は、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挙げることができる。
The nail enamel of the present invention contains, in addition to the above-mentioned essential components, resins, plasticizers and powders (pigments, dyes, pearlescent agents) usually used in cosmetics to the extent that the effects of the present invention are not impaired, if necessary. Etc.), organically modified bentonite, a solvent, an aqueous component, an oily component, an ultraviolet absorber and the like can be added. The nail enamel of the present invention includes nail enamel, enamel top coat,
Examples include enamel base coat.

【0017】[0017]

【実施例】以下に実施例を挙げて更に説明する。なお、
これらは本発明を何ら限定するものではない。
[Examples] Examples will be further described below. In addition,
These do not limit the invention in any way.

【0018】実施例1〜12及び比較例1〜2 表1に示す組成の美爪料を調製し、乾燥性、化粧もち、
塗布膜の艶、発色について官能評価を行った。その結果
も併せて表1に示す。
Examples 1 to 12 and Comparative Examples 1 to 2 A nail enamel having the composition shown in Table 1 was prepared, and the drying property, the makeup lasting property,
A sensory evaluation was performed on the gloss and color development of the coating film. The results are also shown in Table 1.

【0019】[0019]

【表1】 [Table 1]

【0020】(製法)B成分を撹拌混合した後、A成分
を添加し撹拌溶解する。次いで、C成分を添加し、撹拌
分散したものを容器に充填して製品とした。
(Manufacturing method) After mixing the B component with stirring, the A component is added and dissolved by stirring. Next, the component C was added, and the mixture was stirred and dispersed to fill a container to obtain a product.

【0021】(試験方法及び評価方法) a)乾燥性 各試料につき、女性パネル10人(手の爪100部位)
による使用テストにより、一度塗りの時に、塗膜が完全
に乾くまでの時間を比較評価した。
(Test Method and Evaluation Method) a) Dryability For each sample, 10 female panels (100 parts of the nail)
According to the use test according to, the time required for the coating film to dry completely was compared and evaluated once applied.

【0022】b)化粧持ち 化粧もちの評価方法として、パネルを用いた使用テスト
とゴバン目試験により評価した。
B) Makeup Lasting As a method for evaluating makeup lasting, a use test using a panel and an eyelet test were performed.

【0023】b−1)使用テスト 各試料につき、女性パネル10人(手の爪100部位)
による3日間の使用テストを行い評価した。
B-1) Use test For each sample, 10 female panels (100 nails on the hand)
Evaluation was carried out by conducting a usage test for 3 days.

【0024】b−2)ゴバン目試験 硝子板上に、4ミルのドクターブレードを用いて、試料
を均一に塗布し、乾燥後クロスカット試験(1mm×1mmゴ
バン目100個)を用いて3回評価した。
B-2) Goggle test A sample is evenly coated on a glass plate with a 4 mil doctor blade, and after drying, three times using a cross cut test (100 1mm x 1mm goggles). evaluated.

【0025】c)塗布膜の艶 各試料につき、女性パネル10人(手の爪100部位)
による使用テストを行い評価した。
C) Luster of the coating film For each sample, 10 female panels (100 nails on the hand)
It was evaluated by conducting a usage test.

【0026】d)発色 各試料につき、女性パネル10人(手の爪100部位)
による使用テストを行い塗布してから2時間後に評価し
た。
D) Color development Ten female panels (100 nails on the hand) for each sample
The application test was performed and the evaluation was made 2 hours after the application.

【0027】各評価方法につき、上記の絶対評価から得
られた点数を合計し、その平均点をさらに4段階に分け
て評価した。 2.5点以上 :◎ 1.5点以上2.5点未満:○ 0.5点以上1.5点未満:△ 0.5点未満 :×
For each evaluation method, the scores obtained from the above absolute evaluation were totaled, and the average score was further divided into 4 levels for evaluation. 2.5 points or more: ◎ 1.5 points or more and less than 2.5 points: ○ 0.5 points or more and less than 1.5 points: △ less than 0.5 points: ×

【0028】表1の結果から明らかなように、本発明品
である実施例1〜12の美爪料は、比較例1〜2の美爪
料に比較して、発色、艶、乾燥性に優れ、化粧もちの全
ての面で、はるかに優れた特性を有していることがわか
る。特に、実施例1〜3の美爪料は、配合量、配合物質
共に更に好ましい範囲であり、他の実施例4〜12の美
爪料に比較して、更に優れた効果を示していることがわ
かる。
As is clear from the results shown in Table 1, the nail enamel of Examples 1 to 12, which is a product of the present invention, is more excellent in color development, gloss and dryness than the nail enamel of Comparative Examples 1 and 2. It can be seen that it has excellent properties and far superior properties in all aspects of makeup hold. In particular, the nail enamel of Examples 1 to 3 is in a more preferable range both in the compounding amount and the compounding substance, and shows a further excellent effect as compared with the other nail enamel of Examples 4 to 12. I understand.

【0029】[0029]

【発明の効果】本発明の化粧料は、発色、艶に優れ、特
に塗膜の乾燥性及び化粧持ちに優れた美爪料である。
EFFECT OF THE INVENTION The cosmetic of the present invention is a nail enamel excellent in color development and luster, especially in drying property of a coating film and durability of makeup.

Claims (8)

【特許請求の範囲】[Claims] 【請求項1】 硝化綿、可塑剤、溶剤を含有する美爪料
において、シリコーン系樹脂及びアクリル系樹脂及び/
又はスルホンアミド系樹脂を配合することを特徴とする
美爪料。
1. A nail enamel containing nitrified cotton, a plasticizer, and a solvent, which comprises a silicone resin and an acrylic resin and / or
Alternatively, a nail varnish containing a sulfonamide resin.
【請求項2】 シリコーン系樹脂が分子鎖の片末端にラ
ジカル重合性基を有するジメチルポリシロキサン化合物
とアクリル及び/又はメタクリレートを主体とするラジ
カル重合モノマーとをラジカル共重合して得たアクリル
−シリコーン系グラフト共重合体である請求項1記載の
美爪料。
2. An acrylic-silicone obtained by radical-copolymerizing a dimethylpolysiloxane compound having a radical-polymerizable group at one end of a molecular chain of a silicone-based resin and a radical-polymerizable monomer mainly containing acrylic and / or methacrylate. The nail enamel according to claim 1, which is a system-based graft copolymer.
【請求項3】 アクリル系樹脂がアクリル酸アルキル、
メタクリル酸アルキル、アクリル酸、及びメタクリル酸
の中から選ばれる1種以上と、スチレン及びアクリロニ
トリルの中から選ばれる1種又は2種以上とから成る共
重合体である請求項1又は2記載の美爪料。
3. The acrylic resin is an alkyl acrylate,
The beauty according to claim 1 or 2, which is a copolymer consisting of one or more selected from alkyl methacrylate, acrylic acid, and methacrylic acid and one or more selected from styrene and acrylonitrile. Nail charge.
【請求項4】 アクリル系樹脂がアクリル酸ブチルアク
リロニトリルスチレン共重合体である請求項1又は2記
載の美爪料。
4. The nail enamel according to claim 1, wherein the acrylic resin is a butyl acrylonitrile styrene acrylate copolymer.
【請求項5】 スルホンアミド系樹脂がトルエンスルホ
ンアミド樹脂及び/又はトルエンスルホンアミドエポキ
シ樹脂である請求項1〜4のいずれか一項に記載の美爪
料。
5. The nail enamel according to claim 1, wherein the sulfonamide resin is a toluene sulfonamide resin and / or a toluene sulfonamide epoxy resin.
【請求項6】 シリコーン系樹脂を美爪料中に0.2〜
5重量%配合することを特徴とする請求項1〜5のいず
れかに記載の美爪料。
6. A nail resin containing silicone resin in an amount of 0.2 to
It mix | blends 5weight%, The nail enamel in any one of Claims 1-5 characterized by the above-mentioned.
【請求項7】 アクリル系樹脂を美爪料中に1〜15重
量%配合することを特徴とする請求項1〜6のいずれか
に記載の美爪料。
7. The nail enamel according to claim 1, wherein the acrylic resin is mixed in the nail enamel in an amount of 1 to 15% by weight.
【請求項8】 スルホンアミド系樹脂を美爪料中に1〜
25重量%配合することを特徴とする請求項1〜7のい
ずれかに記載の美爪料。
8. Sulfonamide resin is added to the nail varnish in an amount of 1 to
25% by weight is compounded, The nail enamel in any one of Claims 1-7 characterized by the above-mentioned.
JP31416394A 1994-11-24 1994-11-24 Solvent-based nail polish Expired - Fee Related JP3486826B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31416394A JP3486826B2 (en) 1994-11-24 1994-11-24 Solvent-based nail polish

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31416394A JP3486826B2 (en) 1994-11-24 1994-11-24 Solvent-based nail polish

Publications (2)

Publication Number Publication Date
JPH08143427A true JPH08143427A (en) 1996-06-04
JP3486826B2 JP3486826B2 (en) 2004-01-13

Family

ID=18050007

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31416394A Expired - Fee Related JP3486826B2 (en) 1994-11-24 1994-11-24 Solvent-based nail polish

Country Status (1)

Country Link
JP (1) JP3486826B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002068941A (en) * 2000-08-29 2002-03-08 Kose Corp Water in oil type cosmetic
JP2002234822A (en) * 2001-02-09 2002-08-23 Kose Corp Manicure preparation
US6616920B1 (en) 1999-08-23 2003-09-09 Mitsubishi Chemical America, Inc. Nail-care composition containing nail-care polymer
JP2006327941A (en) * 2005-05-23 2006-12-07 Daito Kasei Kogyo Kk Aqueous nail polish

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61210020A (en) * 1985-03-15 1986-09-18 Shiseido Co Ltd Manicure
JPS63284111A (en) * 1987-05-16 1988-11-21 Shiseido Co Ltd Manicure
JPH0225411A (en) * 1988-07-12 1990-01-26 Kobayashi Kose Co Ltd Cosmetic
JPH03112916A (en) * 1989-09-26 1991-05-14 Kanebo Ltd Nail-beautifying agent
JPH0469318A (en) * 1990-07-06 1992-03-04 Shiseido Co Ltd Manicure
JPH0597630A (en) * 1991-10-11 1993-04-20 Kao Corp Water-based nail enamel
JPH05194149A (en) * 1991-07-26 1993-08-03 L'oreal Sa Colorless or colored manicure liquid
JPH0665596A (en) * 1990-06-15 1994-03-08 Shiseido Co Ltd New composite and emulsion composition
WO1994016670A1 (en) * 1993-01-25 1994-08-04 L'oreal Quick-drying coloured or colourless nail varnish

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61210020A (en) * 1985-03-15 1986-09-18 Shiseido Co Ltd Manicure
JPS63284111A (en) * 1987-05-16 1988-11-21 Shiseido Co Ltd Manicure
JPH0225411A (en) * 1988-07-12 1990-01-26 Kobayashi Kose Co Ltd Cosmetic
JPH03112916A (en) * 1989-09-26 1991-05-14 Kanebo Ltd Nail-beautifying agent
JPH0665596A (en) * 1990-06-15 1994-03-08 Shiseido Co Ltd New composite and emulsion composition
JPH0469318A (en) * 1990-07-06 1992-03-04 Shiseido Co Ltd Manicure
JPH05194149A (en) * 1991-07-26 1993-08-03 L'oreal Sa Colorless or colored manicure liquid
JPH0597630A (en) * 1991-10-11 1993-04-20 Kao Corp Water-based nail enamel
WO1994016670A1 (en) * 1993-01-25 1994-08-04 L'oreal Quick-drying coloured or colourless nail varnish

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6616920B1 (en) 1999-08-23 2003-09-09 Mitsubishi Chemical America, Inc. Nail-care composition containing nail-care polymer
JP2002068941A (en) * 2000-08-29 2002-03-08 Kose Corp Water in oil type cosmetic
JP2002234822A (en) * 2001-02-09 2002-08-23 Kose Corp Manicure preparation
JP2006327941A (en) * 2005-05-23 2006-12-07 Daito Kasei Kogyo Kk Aqueous nail polish

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