JPH11240820A - Nail lacquer remover - Google Patents
Nail lacquer removerInfo
- Publication number
- JPH11240820A JPH11240820A JP4170098A JP4170098A JPH11240820A JP H11240820 A JPH11240820 A JP H11240820A JP 4170098 A JP4170098 A JP 4170098A JP 4170098 A JP4170098 A JP 4170098A JP H11240820 A JPH11240820 A JP H11240820A
- Authority
- JP
- Japan
- Prior art keywords
- nail lacquer
- nail
- weight
- solvent
- methyl
- 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
Links
- 239000004922 lacquer Substances 0.000 title claims abstract description 51
- 239000002904 solvent Substances 0.000 claims abstract description 28
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229920001220 nitrocellulos Polymers 0.000 claims abstract description 15
- 239000000020 Nitrocellulose Substances 0.000 claims abstract description 14
- 239000004014 plasticizer Substances 0.000 claims abstract description 14
- 229920005989 resin Polymers 0.000 claims abstract description 9
- 239000011347 resin Substances 0.000 claims abstract description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 238000009835 boiling Methods 0.000 claims description 11
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 claims description 6
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims description 6
- -1 triacetylglyceryl Chemical group 0.000 claims description 5
- HBTAOSGHCXUEKI-UHFFFAOYSA-N 4-chloro-n,n-dimethyl-3-nitrobenzenesulfonamide Chemical compound CN(C)S(=O)(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 HBTAOSGHCXUEKI-UHFFFAOYSA-N 0.000 claims description 3
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 claims description 3
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 claims description 3
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 claims description 3
- 229940031578 diisopropyl adipate Drugs 0.000 claims description 3
- 229940031569 diisopropyl sebacate Drugs 0.000 claims description 3
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 claims description 3
- 229960001826 dimethylphthalate Drugs 0.000 claims description 3
- XFKBBSZEQRFVSL-UHFFFAOYSA-N dipropan-2-yl decanedioate Chemical compound CC(C)OC(=O)CCCCCCCCC(=O)OC(C)C XFKBBSZEQRFVSL-UHFFFAOYSA-N 0.000 claims description 3
- KSCKTBJJRVPGKM-UHFFFAOYSA-N octan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-] KSCKTBJJRVPGKM-UHFFFAOYSA-N 0.000 claims description 3
- WEAPVABOECTMGR-UHFFFAOYSA-N triethyl 2-acetyloxypropane-1,2,3-tricarboxylate Chemical compound CCOC(=O)CC(C(=O)OCC)(OC(C)=O)CC(=O)OCC WEAPVABOECTMGR-UHFFFAOYSA-N 0.000 claims description 3
- 239000001069 triethyl citrate Substances 0.000 claims description 3
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 claims description 3
- 235000013769 triethyl citrate Nutrition 0.000 claims description 3
- LEEDMQGKBNGPDN-UHFFFAOYSA-N 2-methylnonadecane Chemical compound CCCCCCCCCCCCCCCCCC(C)C LEEDMQGKBNGPDN-UHFFFAOYSA-N 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 32
- 235000019441 ethanol Nutrition 0.000 abstract description 18
- 230000002087 whitening effect Effects 0.000 abstract description 14
- 238000004880 explosion Methods 0.000 abstract description 5
- 239000004615 ingredient Substances 0.000 abstract 2
- 238000007788 roughening Methods 0.000 abstract 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 9
- 150000002576 ketones Chemical class 0.000 description 8
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- SYBYTAAJFKOIEJ-UHFFFAOYSA-N 3-Methylbutan-2-one Chemical compound CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 229940072049 amyl acetate Drugs 0.000 description 2
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 2
- 239000010775 animal oil Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 230000003020 moisturizing effect Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 229960000878 docusate sodium Drugs 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、ネイルラッカ−を
除去するために用いられる、いわゆるネイルラッカ−除
去剤に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a so-called nail lacquer remover used for removing nail lacquer.
【0002】[0002]
【従来の技術】ネイルラッカ−の除去を目的とした化粧
品は「マニキュアリム−バ−」、「除光液」の名前で知
られているが、その多くは有機溶剤のアセトンを主成分
とし、助溶剤として酢酸エチル、酢酸アミル、メチルエ
チルケトン、メチルイソブチルケトンを、保湿剤として
グリセリンやプロピレングリコ−ルを配合している。2. Description of the Related Art Cosmetics for the purpose of removing nail lacquer are known under the names of "manicure remover" and "removal remover", and most of them are mainly composed of acetone as an organic solvent. Ethyl acetate, amyl acetate, methyl ethyl ketone and methyl isobutyl ketone are blended as cosolvents, and glycerin and propylene glycol are blended as humectants.
【0003】しかし、主成分として用いているアセトン
は、脱脂力、浸透力、脱水作用が強く、爪の白化や手指
の肌荒れの原因になるばかりか、揮発性が強く引火点も
低いことから爆発や火災の危険性もあり、問題となって
いた。[0003] However, acetone used as a main component has a strong degreasing power, a penetrating power, and a dehydrating effect, and causes not only whitening of nails and rough skin of fingers, but also explosion due to its high volatility and low flash point. And the danger of fire.
【0004】これを改良するネイルラッカ−除去剤とし
て、プロピレンカ−ボネ−トとエタノ−ルとを主成分
とし、これに水と少量のヒドロキシプロピルセルロ−ス
を添加してゲル状にしたもの(特開平1−242515
号公報)、炭酸エチレン、低級一価アルコ−ル及びケ
トン類を含有するもの(特開平9−169621号公
報)、ピロリドン系有機溶剤(実施例はN−メチル−
2−ピロリドンを使用)及び水を含むもの(特開平7−
109210号公報)、N−メチル−2−ピロリドン
とd−リモネンとエタノ−ルを含有するもの(特開平1
−135710号公報)が開示されている。As a nail lacquer remover for improving this, propylene carbonate and ethanol are used as main components, and a gel is formed by adding water and a small amount of hydroxypropyl cellulose. (Japanese Patent Laid-Open No. 1-242515
Japanese Patent Application Laid-Open No. 9-169621), those containing ethylene carbonate, lower monohydric alcohols and ketones (JP-A-9-169621), and pyrrolidone-based organic solvents (Examples include N-methyl-
Containing 2-pyrrolidone) and water (Japanese Unexamined Patent Publication No.
No. 109210), those containing N-methyl-2-pyrrolidone, d-limonene and ethanol (Japanese Patent Laid-Open No.
-135710).
【0005】しかし、いずれの除去剤も、ネイルラッカ
−の主成分たるニトロセルロ−スを除去するための主た
る溶剤が、プロピレンカ−ボネ−ト、炭酸エチレン、N
−メチル−2−ピロリドンといった高沸点溶剤であり、
ネイルラッカ−の除去直後の乾燥性が悪く、「べたつ
き」といった高沸点溶剤の残留感を、その使用者に与え
る欠点があった。特に、は従来のケトン類を含むもの
で、前記ケトン類の問題点の改良性においても十分でな
いものである。[0005] However, the main solvent for removing nitrocellulose which is a main component of nail lacquer is propylene carbonate, ethylene carbonate, N
A high boiling solvent such as -methyl-2-pyrrolidone,
The drying property immediately after the removal of the nail lacquer is poor, and there is a drawback that a feeling of residual high boiling solvent such as "stickiness" is given to the user. In particular, contains ketones of the prior art, and is not satisfactory in improving the problems of the ketones.
【0006】[0006]
【発明が解決しようとする課題】そこで、本発明は、除
去性能が高くてべたつき感がなく、しかも爪の白化や手
指の肌荒れがなく、爆発や火災の危険性もほとんどない
ネイルラッカ−除去剤を提供することを目的とするもの
である。SUMMARY OF THE INVENTION Accordingly, the present invention is directed to a nail lacquer-removing agent which has a high removal performance, has no sticky feeling, has no whitening of nails and rough skin of fingers, and has almost no danger of explosion or fire. The purpose is to provide.
【0007】[0007]
【課題を解決するための手段】かかる目的を達成するた
め、鋭意研究した結果、アセトンのような有害性がな
く、しかも乾燥しやすいエチルアルコ−ルを主成分し、
これに従来より比較的少量のN−メチル−2−ピロリド
ンとネイルラッカ−の成分たるニトロセルロ−スの可塑
剤やネイルラッカ−の他の成分の溶剤を配合すれば、ネ
イルラッカ−除去効果を十分示すばかりでなく、べたつ
き感が生じないネイルラッカ−除去剤が得られることを
見出だし本発明を完成させた。To achieve this object, as a result of intensive studies, it has been found that ethyl alcohol, which has no harmfulness like acetone and is easy to dry, is used as a main component.
If a relatively small amount of N-methyl-2-pyrrolidone and a plasticizer of nitrocellulose, which is a component of the nail lacquer, or a solvent of another component of the nail lacquer are blended, a sufficient effect of removing the nail lacquer can be obtained. In addition to the above, it has been found that a nail lacquer-removing agent which does not cause stickiness can be obtained, and the present invention has been completed.
【0008】すなわち、本発明のうち請求項1記載の発
明は、少なくとも、エチルアルコ−ルの50〜70重量
%と、N−メチル−2−ピロリドンの10〜30重量%
と、ネイルラッカ−成分であるニトロセルロ−スの可塑
剤及び/又はネイルラッカ−の他の樹脂成分の溶剤から
選ばれた一種又は二種以上の10〜30重量%とを、含
有してなるネイルラッカ−除去剤である。That is, the invention according to claim 1 of the present invention comprises at least 50 to 70% by weight of ethyl alcohol and 10 to 30% by weight of N-methyl-2-pyrrolidone.
And a nail varnish comprising one or more selected from the group consisting of a plasticizer of nitrocellulose as a nail lacquer component and / or a solvent of another resin component of the nail lacquer, in an amount of 10 to 30% by weight. It is a lacquer-removing agent.
【0009】ここで、ネイルラッカ−とは、ニトロセル
ロ−スを成分とする爪への塗剤であれば、特に限定され
ないが、樹脂成分としてニトロセルロ−スを主成分とす
るものが好ましい。通常使用されるものとしては、ニト
ロセルロ−スが主体であって、アルキッド樹脂、アクリ
ル樹脂を併用したものを樹脂成分とし、溶剤としてアセ
トン、メチルエチルケトン、メチルイソプロピルケトン
等のケトン類や酢酸エチル、酢酸ブチル、酢酸アミル等
の酢酸エステルを用いたものが例示される。Here, the nail lacquer is not particularly limited as long as it is a coating composition for nails containing nitrocellulose as a component, but a resin containing nitrocellulose as a main component as a resin component is preferable. Usually, nitrocellulose is mainly used, and alkyd resin and acrylic resin are used as a resin component, and ketones such as acetone, methyl ethyl ketone and methyl isopropyl ketone, and ethyl acetate and butyl acetate are used as solvents. And those using an acetate such as amyl acetate.
【0010】本発明において用いるエチルアルコ−ルの
含有量は、50〜70重量%とする必要がある。50重
量%未満では、本発明に係る除去剤使用直後(拭き取り
直後)の溶剤の乾燥性が十分でなく、べたつき感が残存
する一方、70重量%を超えるとネイルラッカ−の除去
性能が十分でなくなるからである。また、N−メチル−
2−ピロリドンの含有量は10〜30重量%とする必要
がある。10重量%未満では、ネイルラッカ−の除去性
能が十分でなくなる一方、30重量%を超えると、前記
拭き取り直後の溶剤の乾燥性が十分でなく、べたつき感
が残存することになるからである。[0010] The content of ethyl alcohol used in the present invention must be 50 to 70% by weight. If the amount is less than 50% by weight, the drying property of the solvent immediately after the use of the remover according to the present invention (immediately after wiping) is not sufficient, and a sticky feeling remains. On the other hand, if it exceeds 70% by weight, nail lacquer removal performance is sufficient. Because it is gone. Also, N-methyl-
The content of 2-pyrrolidone must be 10 to 30% by weight. If the amount is less than 10% by weight, the performance of removing nail lacquer will not be sufficient, while if it exceeds 30% by weight, the drying property of the solvent immediately after the wiping will be insufficient and the sticky feeling will remain.
【0011】本発明において用いる、ネイルラッカ−成
分であるニトロセルロ−スの可塑剤は、ニトロセルロ−
スの可塑剤として使用可能なものであれば特に限定され
ないが、請求項2記載の発明のように、フタル酸ジメチ
ル、フタル酸ジブチル、フタル酸ジオクチル、アジピン
酸ジイソプロピル、セバシン酸ジエチル、セバシン酸ジ
イソプロピル、クエン酸アセチルトリエチル、クエン酸
トリエチル、トリアセチルグリセリルであることが好ま
しい。The plasticizer of nitrocellulose which is a nail lacquer component used in the present invention is nitrocellulose.
No particular limitation is imposed as long as it can be used as a plasticizer for styrene, but as in the invention of claim 2, dimethyl phthalate, dibutyl phthalate, dioctyl phthalate, diisopropyl adipate, diethyl sebacate, diisopropyl sebacate , Acetyl triethyl citrate, triethyl citrate and triacetyl glyceryl are preferred.
【0012】また、ネイルラッカ−の他の樹脂成分の溶
剤は、他の樹脂(例えば、アルキッド樹脂、アクリル樹
脂)の溶剤として使用可能なものであれば特に限定され
ないが、請求項3記載の発明のように、沸点が60〜2
60℃程度の軽質流動イソパラフィンであることが好ま
しい。The solvent of the other resin component of the nail lacquer is not particularly limited as long as it can be used as a solvent of another resin (for example, an alkyd resin or an acrylic resin). The boiling point is 60-2
It is preferably light liquid isoparaffin at about 60 ° C.
【0013】これらの可塑剤及び溶剤はそれぞれ単独で
用いてもよいし、2種以上を併用してもよい。但し、可
塑剤及び/又は溶剤の含有量は10〜30重量%とする
必要がある。10重量%未満ではネイルラッカ−の除去
性能が十分でなくなる一方、70重量%を超えると前記
拭き取り直後の溶剤の乾燥性が十分でなくなるからであ
る。These plasticizers and solvents may be used alone or in combination of two or more. However, the content of the plasticizer and / or the solvent needs to be 10 to 30% by weight. If the amount is less than 10% by weight, the performance of removing the nail lacquer will not be sufficient, while if it exceeds 70% by weight, the drying property of the solvent immediately after the wiping will be insufficient.
【0014】本発明においては、少なくとも、以上のよ
うに構成されていればよく、使用目的に応じ、これらに
加えて、ネイルラッカ−の溶解能力を向上さすための浸
透剤、分散剤、可溶化剤としての種々の界面活性剤、エ
チルアルコ−ルとの相溶性を付与するためのカップリン
グ剤や揮発速度調節剤としてのグリコ−ルエ−テル、揮
発速度調節剤としてのアルコ−ル類等を含有してもよ
く、また、使用時の利便性を考慮し、増粘剤を添加して
「液だれ」を少なくすることもできる。さらに、爪、手
指の保護や保湿の目的で、グリセリン、ソルビト−ル等
の多価アルコ−ル、グリコ−ル類、動植物油、炭化水素
を含有さすこともできる。In the present invention, it is sufficient that the composition is at least as described above. Depending on the purpose of use, in addition to these, a penetrating agent, a dispersant, and a solubilizing agent for improving the dissolving ability of nail lacquer. Contains various surfactants as agents, coupling agents for imparting compatibility with ethyl alcohol, glycol ethers as volatilization rate regulators, alcohols as volatilization rate regulators, etc. Alternatively, in consideration of convenience at the time of use, a thickener may be added to reduce "drips". Further, for the purpose of protecting nails and fingers and moisturizing, it may contain polyhydric alcohols such as glycerin and sorbitol, glycols, animal and vegetable oils, and hydrocarbons.
【0015】本発明のネイルラッカ−除去剤は、請求項
1、請求項2又は請求項3のように構成することによ
り、従来のアセトン等のケトン類を使用せず、エチルア
ルコ−ルを主成分としているので、爪の白化や手指の肌
荒れがなく、爆発や火災の危険性もほとんどなく、しか
も、N−メチル−2−ピロリドンの含有量を従来より減
少させると共にネイルラッカ−の成分であるニトロセル
ロ−スの可塑剤やネイルラッカ−の他の成分の溶剤の所
定量を含有させたことにより、高沸点溶剤の減少と前記
可塑剤及び/又は前記溶剤による作用が相俟って、従来
のように、N−メチル−2−ピロリドンに基づく「べた
つき感」が生じないばかりか、ケトン類を用いた場合と
同様のネイルラッカ−の除去効果を示す。The nail lacquer-removing agent of the present invention comprises ethyl alcohol as a main component without using a conventional ketone such as acetone by constituting as described in claim 1, 2 or 3. Therefore, there is no whitening of nails and rough skin of fingers, there is almost no danger of explosion or fire, moreover, the content of N-methyl-2-pyrrolidone is reduced than before and nitrocellulo, a component of nail lacquer, is reduced. A predetermined amount of a solvent of a plasticizer or other components of a nail lacquer, the reduction of the high boiling point solvent and the action of the plasticizer and / or the solvent are combined, as in the conventional method. In addition to the fact that "stickiness" based on N-methyl-2-pyrrolidone does not occur, the same effect of removing nail lacquer as in the case of using ketones is shown.
【0016】すなわち、本発明のネイルラッカ−除去剤
は、ネイルラッカ−に対し溶解性能の優れている高沸
点溶剤(N−メチル−2−ピロリドン)の含有量を最小
限にしつつ、しかもネイルラッカ−に対する溶解性は低
いがアセトンのような弊害がなく、高沸点溶剤との相溶
性がよくて高沸点溶剤の揮発性を高めるエチルアルコ−
ルを、従来より多く含有させたことにより、高沸点溶剤
によるネイルラッカ−溶解機能の最大限の発揮とその揮
発機能の向上を図りつつ、ネイルラッカ−中のニトロ
セルロ−スの可塑剤や他の成分の溶剤を含有させネイル
ラッカ−の除去機能を高めたたものであり、これら
の作用が相俟って、ネイルラッカ−に対する良好な除去
機能と使用者にべたつき感をもたらさない効果を達成し
たものである。That is, the nail lacquer remover of the present invention minimizes the content of a high boiling solvent (N-methyl-2-pyrrolidone) having excellent dissolving performance for nail lacquer, Ethyl alcohol which has low solubility in-but has no adverse effects like acetone, has good compatibility with high-boiling solvents and enhances the volatility of high-boiling solvents-
By increasing the content of nitrocellulose in the nail lacquer, it is possible to maximize the dissolution function of the nail lacquer and improve the volatilization function by using a high boiling point solvent. The composition contains a solvent as a component and enhances the function of removing nail lacquer, and together with these actions, achieved a good removal function for nail lacquer and an effect of not giving the user a sticky feeling. Things.
【0017】[0017]
【発明の実施の形態】以下、本発明の実施の形態につい
て説明する。本発明に係るネイルラッカ−除去剤は、少
なくとも、エチルアルコ−ルの50〜70重量%好まし
くは60〜65重量%と、N−メチル−2−ピロリドン
の10〜30重量%好ましくは15〜25重量%と、フ
タル酸ジメチル、フタル酸ジブチル、フタル酸ジオクチ
ル、アジピン酸ジイソプロピル、セバシン酸ジエチル、
セバシン酸ジイソプロピル、クエン酸アセチルトリエチ
ル、クエン酸トリエチル若しくはトリアセチルグリセリ
リルであるニトロセルロ−スの可塑剤及び/又は沸点が
60〜260℃の軽質流動イソパラフィンから選ばれた
一種若しくは二種以上の10〜30重量%好ましくは1
0〜20重量%とを、常法により混合すれば、製造でき
る。Embodiments of the present invention will be described below. The nail lacquer remover according to the present invention comprises at least 50 to 70% by weight, preferably 60 to 65% by weight of ethyl alcohol and 10 to 30% by weight, preferably 15 to 25% by weight of N-methyl-2-pyrrolidone. % And dimethyl phthalate, dibutyl phthalate, dioctyl phthalate, diisopropyl adipate, diethyl sebacate,
A plasticizer of nitrocellulose, which is diisopropyl sebacate, acetyltriethyl citrate, triethyl citrate or triacetylglyceryl, and / or one or more of 10 to 10 kinds of light liquid isoparaffins having a boiling point of 60 to 260 ° C. 30% by weight, preferably 1
It can be produced by mixing 0 to 20% by weight with a conventional method.
【0018】なお、必要に応じ、上記のものに加えて、
ネイルラッカ−の溶解能力を向上さすための浸透剤、分
散剤、可溶化剤としての種々の界面活性剤を含有させて
もよい。これらの界面活性剤としては、ジオクチルスル
ホコハク酸塩、ポリオキシエチレン硬化ヒマシ油等を例
示できる。If necessary, in addition to the above,
Various surfactants as penetrants, dispersants, and solubilizers for improving the dissolving ability of the nail lacquer may be contained. Examples of these surfactants include dioctyl sulfosuccinate, polyoxyethylene hydrogenated castor oil, and the like.
【0019】また、エチルアルコ−ルとの相溶性を付与
するためのカップリング剤や揮発速度調節剤としての機
能を有するグリコ−ルエ−テル、揮発速度調節剤として
のアルコ−ル類等を含有させてもよく、また、使用時の
利便性を考慮し、増粘剤を添加して「液だれ」を少なく
することもできる。Also, a glycol ether having a function as a coupling agent for imparting compatibility with ethyl alcohol or a volatilization rate regulator, alcohols as a volatilization rate regulator, etc. are contained. Alternatively, in consideration of the convenience at the time of use, a thickener may be added to reduce "drips".
【0020】さらに、爪、手指の保護や保湿の目的で、
グリセリン、ソルビト−ル等の多価アルコ−ル、グリコ
−ル類、動植物油、炭化水素を含有さすこともできる。Furthermore, for the purpose of protecting nails and fingers and moisturizing,
It may also contain polyhydric alcohols such as glycerin and sorbitol, glycols, animal and vegetable oils, and hydrocarbons.
【0021】上記のようにして製造した本発明のネイル
ラッカ−除去剤は、脱脂綿に含ませ、これを用いて市販
のネイルラッカ−を塗布した爪を拭けば、爪からネイル
ラッカ−が簡単に除去でき、爪の白化、手指の肌荒れが
なく、かつ、べたつき感も残らない。The nail lacquer remover of the present invention produced as described above is contained in absorbent cotton, and the nail lacquer is coated with a commercially available nail lacquer. It can be removed, there is no whitening of nails, no rough skin on fingers, and no sticky feeling remains.
【0022】[0022]
【実施例】次に、実施例をもって、本発明をさらに具体
的に説明する。なお、表1、2において、各除去剤の成
分の数値は重量%を示す。Next, the present invention will be described more specifically with reference to examples. In addition, in Tables 1 and 2, the numerical values of the components of each removing agent indicate% by weight.
【0023】(実施例)表1に示す組成となるように、
それぞれの成分を均一に混合してネイルラッカ−除去剤
を調節し、本発明品(実施例1〜10)を得た。 (比較例)表2に示す組成となるように、それぞれの成
分を均一に混合してネイルラッカ−除去剤を調節し、比
較品(比較例1〜3)を得た。(Example) In order to obtain the composition shown in Table 1,
The components were uniformly mixed to adjust the nail lacquer-removing agent, thereby obtaining the products of the present invention (Examples 1 to 10). (Comparative Example) The components were uniformly mixed so that the compositions shown in Table 2 were obtained, and the nail lacquer-removing agent was adjusted to obtain comparative products (Comparative Examples 1 to 3).
【0024】(試験方法)ネイルラッカ−(ジョイン株
式会社製メロディユメイクカラ−、ネイル)を爪に塗布
し24時間放置後、4cm×4cmの脱脂綿に実施例1
〜10、比較例1〜3の除去剤1mlを含ませて爪の表
面を軽く撫でて拭き取り、ネイルラッカ−の除去性を観
察した。また、ネイルラッカ−除去後の爪の白化、手指
の肌荒れ、べたつき感を評価した。結果を表1、2に示
す。(Test Method) A nail lacquer (Melody Make Color, made by Join Co., Ltd., nail) was applied to nails and allowed to stand for 24 hours.
10 and 1 ml of the removers of Comparative Examples 1 to 3 were gently stroked on the surface of the nail and wiped off to observe the nail lacquer removability. In addition, the whitening of the nails after the removal of the nail lacquer, the rough skin of the fingers, and the stickiness were evaluated. The results are shown in Tables 1 and 2.
【0025】(除去性) 肉眼により観察し、次の4段
階評価を行った。 ×:非常に落ちにくい。 △:やや落ちにくい。 ○:よく落ちる ◎:非常によく落ちる。(Removability) Observation was made with the naked eye, and the following four grades were evaluated. X: Very hard to fall. Δ: Slightly hard to drop. :: falls well ◎: falls very well.
【0026】(べたつき感) 次の3段階の官能評価を
行った。 ×:べたつきが明確に認められる。 △:べたつきが×と○の間である。 ○:べたつきが認められない。(Stickiness) The following three levels of sensory evaluation were performed. X: Stickiness is clearly recognized. Δ: Stickiness is between × and ○. :: No stickiness was observed.
【0027】(爪の白化、手指の肌荒れ) 肉眼観察に
より次の2段階評価を行った。 ×:爪の白化及び/又は手指の肌荒れが明確に認められ
る。 △:爪の白化及び/又は手指の肌荒れが×と○の間であ
る。 ○:爪の白化及び/又は手指の肌荒れが認められない。(Whitening of nails, rough skin of fingers) The following two-stage evaluation was performed by visual observation. ×: Whitening of nails and / or rough skin of fingers are clearly observed. Δ: Whitening of nails and / or rough skin of fingers are between × and ○. :: No whitening of nails and / or rough skin of fingers are observed.
【0028】[0028]
【表1】 [Table 1]
【0029】[0029]
【表2】 [Table 2]
【0030】表1に示す評価より、本発明に係るネイル
ラッカ−除去剤(実施例1〜8)は、いずれも、ネイル
ラッカ−の除去性がよく、べたつき感が認められず、爪
の白化や手指の肌荒れも認められない。From the evaluations shown in Table 1, all of the nail lacquer removers according to the present invention (Examples 1 to 8) have good nail lacquer removal properties, no sticky feeling, and whitening of nails. Also, rough skin of fingers and hands is not recognized.
【0031】しかし、表2に示すように、従来のエチル
アルコ−ルとN−メチル−2−ピロリドンとd−リモネ
ンを構成成分とする除去剤(比較例4)は、ネイルラッ
カ−の除去性や爪の白化等を生じない点では優れている
ものの、べたつき感が明確に認められ、また、エチルア
ルコ−ルとアセトンと炭酸エチレンを構成成分とするも
の(比較例5)は除去性は優れているものの爪の白化等
が明確に認められ、べたつき感も残る場合がある。次
に、本発明に係る構成成分のいずれをも含む除去剤であ
っても、エチルアルコ−ルが70重量%を超えるもの
(比較例1)は、除去性において、50重量%未満のも
の(比較例3)は、べたつき感において十分でなく、本
発明の他の構成要件を具備するがN−メチル−2−ピロ
リドンを含まない除去剤(比較例2)は、除去性におい
て十分でない。However, as shown in Table 2, the conventional remover containing ethyl alcohol, N-methyl-2-pyrrolidone and d-limonene as components (Comparative Example 4) was not effective in removing nail lacquer. Although it is excellent in that it does not cause whitening of the nails, etc., a sticky feeling is clearly recognized, and the one containing ethyl alcohol, acetone and ethylene carbonate (Comparative Example 5) has excellent removability. However, whitening or the like of the nail is clearly recognized, and a sticky feeling may remain. Next, among the removing agents containing any of the constituents according to the present invention, those having an ethyl alcohol content of more than 70% by weight (Comparative Example 1) have a removability of less than 50% by weight (Comparative Example 1). Example 3) is not sufficient in stickiness, and the other remover containing N-methyl-2-pyrrolidone (Comparative Example 2) does not have sufficient removability.
【0032】[0032]
【発明の効果】以上説明したように、本発明のネイルラ
ッカ−除去剤は、請求項1、請求項2又は請求項3のよ
うに構成することにより、第1に従来のアセトン等のケ
トン類を使用せず、エチルアルコ−ルを主成分としてい
るので、爪の白化や手指の肌荒れがなく、爆発や火災の
危険性もほとんどなく、第2にネイルラッカ−に対し溶
解性能の優れているもののべたつき感の原因となるN−
メチル−2−ピロリドンの含有量を従来より減少させる
と共にニトロセルロ−スの可塑剤やネイルラッカ−の他
の成分の溶剤の所定量を含有させたことにより、高沸点
溶剤の減少と前記可塑剤及び/又は前記溶剤による作用
が相俟って、N−メチル−2−ピロリドンに基づく「べ
たつき感」が生じないばかりか、ケトン類を用いた場合
と同様に優れたネイルラッカ−の除去効果を示す。As described above, the nail lacquer-removing agent of the present invention is constituted by the first, second or third aspect of the present invention, and thus, firstly, the conventional ketones such as acetone. No ethyl alcohol is used as the main component, so there is no whitening of nails or rough skin of fingers, there is almost no danger of explosion and fire, and secondly, it has excellent dissolving performance for nail lacquer. N- causes stickiness
By reducing the content of methyl-2-pyrrolidone and adding a predetermined amount of a nitrocellulose plasticizer and a solvent of other components of nail lacquer, the amount of the high boiling point solvent is reduced and the plasticizer and And / or the effect of the solvent described above not only does not give a "sticky feeling" based on N-methyl-2-pyrrolidone, but also exhibits an excellent nail lacquer removal effect as in the case of using ketones. .
Claims (3)
70重量%と、N−メチル−2−ピロリドンの10〜3
0重量%と、ネイルラッカ−成分であるニトロセルロ−
スの可塑剤及び/又はネイルラッカ−の他の樹脂成分の
溶剤から選ばれた一種又は二種以上の10〜30重量%
とを、含有してなるネイルラッカ−除去剤。(1) at least 50-ethyl alcohol;
70% by weight and 10 to 3 of N-methyl-2-pyrrolidone.
0% by weight and nitrocellulose as a nail lacquer component
10 to 30% by weight of one or more selected from solvents of plasticizers and / or other resin components of nail lacquer
And a nail lacquer-removing agent.
ルロ−スの可塑剤が、フタル酸ジメチル、フタル酸ジブ
チル、フタル酸ジオクチル、アジピン酸ジイソプロピ
ル、セバシン酸ジエチル、セバシン酸ジイソプロピル、
クエン酸アセチルトリエチル、クエン酸トリエチル、ト
リアセチルグリセリルであることを特徴とする請求項1
記載のネイルラッカ−除去剤。2. The plasticizer for nitrocellulose, which is a nail lacquer component, comprises dimethyl phthalate, dibutyl phthalate, dioctyl phthalate, diisopropyl adipate, diethyl sebacate, diisopropyl sebacate,
2. An acetyltriethyl citrate, triethyl citrate, and triacetylglyceryl.
The nail lacquer-removing agent according to the above.
剤が、沸点が60〜260℃程度の軽質流動イソパラフ
ィンであることを特徴とする請求項1又は2記載のネイ
ルラッカ−除去剤。3. The nail lacquer remover according to claim 1, wherein the solvent of the other resin component of the nail lacquer is light liquid isoparaffin having a boiling point of about 60 to 260 ° C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4170098A JPH11240820A (en) | 1998-02-24 | 1998-02-24 | Nail lacquer remover |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4170098A JPH11240820A (en) | 1998-02-24 | 1998-02-24 | Nail lacquer remover |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH11240820A true JPH11240820A (en) | 1999-09-07 |
Family
ID=12615709
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4170098A Pending JPH11240820A (en) | 1998-02-24 | 1998-02-24 | Nail lacquer remover |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH11240820A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102166165A (en) * | 2010-02-25 | 2011-08-31 | 林任猛 | An environmentally friendly water-based nail polish remover |
| JP2023079572A (en) * | 2021-11-29 | 2023-06-08 | 株式会社 資生堂 | Oil-in-water emulsified cosmetic |
-
1998
- 1998-02-24 JP JP4170098A patent/JPH11240820A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102166165A (en) * | 2010-02-25 | 2011-08-31 | 林任猛 | An environmentally friendly water-based nail polish remover |
| JP2023079572A (en) * | 2021-11-29 | 2023-06-08 | 株式会社 資生堂 | Oil-in-water emulsified cosmetic |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5372742A (en) | Nail polish remover | |
| US4120810A (en) | Paint remover with improved safety characteristics | |
| US4801331A (en) | Nail lacquer remover composition | |
| JPH0899839A (en) | Nail polish remover | |
| US5346652A (en) | Nail polish remover composition | |
| US5360580A (en) | Cleaning composition | |
| JP2013241362A (en) | Remover for nail coating agent and removing method | |
| JP2002536307A (en) | Remover for adhesive products | |
| US20100204076A1 (en) | Gelled nail polish remover | |
| US7074746B2 (en) | Nail polish remover | |
| EP0785764A1 (en) | Enamel remover | |
| JPH11240820A (en) | Nail lacquer remover | |
| WO2014119039A1 (en) | Oil-based liquid cleansing composition | |
| WO2002016539A1 (en) | Nail polish remover | |
| KR970002606B1 (en) | Deodorizing type odorless nail enamel remover composition | |
| JP2016160187A (en) | Skin protective agents for hair dye | |
| JP3220968B2 (en) | Transparent liquid hair styling composition | |
| JP3464045B2 (en) | Low alcohol flavor composition | |
| KR20020047127A (en) | Non-ethanolic composition comprising a hydrofluoro ether | |
| WO1993018734A1 (en) | Nail polish remover composition | |
| JPH1036227A (en) | Nail enamel remover | |
| JPH05163116A (en) | Removing agent for eye makeup | |
| JP3122231B2 (en) | Cloudy enamel remover | |
| JP3251675B2 (en) | Low alcohol fragrance composition | |
| JP2000095646A (en) | Nail enamel remover in gel state |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Effective date: 20041102 Free format text: JAPANESE INTERMEDIATE CODE: A621 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20051122 |
|
| A131 | Notification of reasons for refusal |
Effective date: 20051129 Free format text: JAPANESE INTERMEDIATE CODE: A131 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20060221 |