JPS6324969B2 - - Google Patents
Info
- Publication number
- JPS6324969B2 JPS6324969B2 JP29325485A JP29325485A JPS6324969B2 JP S6324969 B2 JPS6324969 B2 JP S6324969B2 JP 29325485 A JP29325485 A JP 29325485A JP 29325485 A JP29325485 A JP 29325485A JP S6324969 B2 JPS6324969 B2 JP S6324969B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- remover
- enamel
- fatty acid
- ester
- 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
Links
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 35
- 229930195729 fatty acid Natural products 0.000 claims description 35
- 239000000194 fatty acid Substances 0.000 claims description 35
- 210000003298 dental enamel Anatomy 0.000 claims description 32
- -1 sucrose fatty acid ester Chemical class 0.000 claims description 19
- 150000004665 fatty acids Chemical class 0.000 claims description 17
- 229930006000 Sucrose Natural products 0.000 claims description 15
- 150000002148 esters Chemical class 0.000 claims description 14
- 239000005720 sucrose Substances 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 150000001298 alcohols Chemical class 0.000 claims description 6
- 150000002334 glycols Chemical class 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 239000006184 cosolvent Substances 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 16
- 235000019441 ethanol Nutrition 0.000 description 15
- 229960004793 sucrose Drugs 0.000 description 14
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 10
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 9
- 235000021355 Stearic acid Nutrition 0.000 description 8
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 8
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 239000008117 stearic acid Substances 0.000 description 8
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000006071 cream Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 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 description 5
- 235000021314 Palmitic acid Nutrition 0.000 description 5
- 229940031578 diisopropyl adipate Drugs 0.000 description 5
- 229960000735 docosanol Drugs 0.000 description 5
- 238000004945 emulsification Methods 0.000 description 5
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 4
- 150000005690 diesters Chemical class 0.000 description 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
- 210000004400 mucous membrane Anatomy 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 235000021360 Myristic acid Nutrition 0.000 description 3
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
- 239000002932 luster Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000008213 purified water Substances 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229960000541 cetyl alcohol Drugs 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000008240 homogeneous mixture Substances 0.000 description 2
- 230000007794 irritation Effects 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- 150000005691 triesters Chemical class 0.000 description 2
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- RDOFJDLLWVCMRU-UHFFFAOYSA-N Diisobutyl adipate Chemical compound CC(C)COC(=O)CCCCC(=O)OCC(C)C RDOFJDLLWVCMRU-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 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
- 239000004909 Moisturizer Substances 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- 239000011928 denatured alcohol Substances 0.000 description 1
- 229940031769 diisobutyl adipate Drugs 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000004744 fabric Substances 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
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229940012831 stearyl alcohol Drugs 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
Description
【発明の詳細な説明】
(a) 発明の目的
本発明は美爪エナメル(通称マニキユア)の除
去剤に関する。DETAILED DESCRIPTION OF THE INVENTION (a) Object of the Invention The present invention relates to a remover for beautiful nail enamel (commonly known as manicure).
(従来の技術)
従来、美爪エナメル除去剤としては、揮発性の
低沸点溶剤、たとえば酢酸エチル、酢酸ブチル、
アセトン、メチルエチルケトン及びメチルイソブ
チルケトン等を主成分とするものが使用されてい
た。しかし、かかる揮発性の低沸点溶剤を主成分
とする美爪エナメル除去剤は、溶剤臭が強くて、
目、鼻、咽喉等の粘膜への刺激が強く、また皮ふ
に附着すると皮ふの油分や水分を過度に除去して
しまうなどの欠点があるばかりでなく、エナメル
除去後の爪の油分や水分を除去してしまい、爪の
光沢をなくしたり、爪を白化させたり、爪をもろ
くさせるなどの欠点があつた。(Prior Art) Conventionally, as nail enamel removers, volatile low-boiling solvents such as ethyl acetate, butyl acetate,
Those containing acetone, methyl ethyl ketone, methyl isobutyl ketone, etc. as main components were used. However, nail enamel removers whose main ingredients are volatile low-boiling solvents have a strong solvent odor.
Not only is it highly irritating to the mucous membranes of the eyes, nose, throat, etc., and if it gets on the skin, it removes too much oil and water from the skin, but it also removes oil and water from the nails after enamel has been removed. It has the disadvantages of removing the nails, causing the nails to lose their luster, turn white, and make the nails brittle.
(発明が解決しようとする問題点)
本発明は、溶剤臭が少なく、目、鼻、咽喉など
の粘膜に対する刺激が少なく、皮ふや美爪エナメ
ル除去後の爪の油分や水分を過度に除去するおそ
れがなく、しかもエナメル除去効果の優れた美爪
エナメル除去剤を提供しようとするものである。(Problems to be Solved by the Invention) The present invention has less solvent odor, less irritation to mucous membranes such as the eyes, nose, and throat, and removes excessive oil and water from the skin and nails after removing beautiful nail enamel. The purpose of the present invention is to provide a beautiful nail enamel remover that is free from danger and has an excellent enamel removal effect.
(b) 発明の構成
(問題点を解決するための手段)
本発明者等は、前記の問題点を解決するために
種々研究を重ねた結果、特定の組成からなる美爪
エナメル除去剤によりその目的を達成することが
できたのである。(b) Structure of the Invention (Means for Solving the Problems) As a result of repeated research in order to solve the above-mentioned problems, the present inventors have succeeded in solving the above-mentioned problems using a beautiful nail enamel remover having a specific composition. I was able to achieve my goal.
すなわち、本発明の美爪エナメル除去剤は、高
級脂肪酸2〜6重量%、高級アルコール5〜10重
量%、シヨ糖脂肪酸エステル5〜8重量%、炭素
数が10以上の脂肪酸エステル30〜70重量%、グリ
コール類3〜8重量%、パラオキシ安息香酸エス
テル0.2〜0.4重量%、残部が水及び必要に応じて
添加する助溶剤よりなるものである。 That is, the beautiful nail enamel remover of the present invention contains 2 to 6% by weight of higher fatty acids, 5 to 10% by weight of higher alcohols, 5 to 8% by weight of sucrose fatty acid esters, and 30 to 70% by weight of fatty acid esters having 10 or more carbon atoms. %, glycols 3 to 8% by weight, paraoxybenzoic acid ester 0.2 to 0.4% by weight, and the balance consists of water and a co-solvent added as necessary.
本発明の美爪エナメル除去剤により爪に塗布さ
れたエナメルを除去するには、除去すべきエナメ
ルの塗布された爪に除去剤を少量施して爪全体に
のばし、暫く放置してから布又はテイツシユペー
パー等で拭き取れば、極めて容易にエナメルを除
去できる。そして、その場合に不快な臭気が殆ん
どなく、目、鼻、咽喉等の粘膜を刺激するおそれ
がない。また、エナメル除去後の爪が油分及び水
分の過度の除去によつて光沢を失なつたり、白化
したり、もろくなつたりするおそれがないし、皮
ふに附着しても皮ふの油分や水分を過度に除去し
て皮ふを荒らすおそれもない。 To remove the enamel applied to the nails using the beautiful nail enamel remover of the present invention, apply a small amount of the remover to the nail that has the enamel to be removed, spread it over the entire nail, leave it for a while, and then use a cloth or nail polisher. Enamel can be removed very easily by wiping it with gloss paper. In this case, there is almost no unpleasant odor, and there is no risk of irritation to the mucous membranes of the eyes, nose, throat, etc. In addition, there is no risk that the nails after enamel will lose their luster, turn white, or become brittle due to excessive removal of oil and moisture, and even if the nails are attached to the skin, they will not remove excessive oil and moisture from the skin. There is no risk of removing it and irritating the skin.
本発明の美爪エナメル除去剤の各成分について
説明すると、高級脂肪酸及び高級アルコールは、
協同して除去剤(クリーム)の展延性を高め、除
去剤の使用感を良好にするとともに、除去剤全体
の乳化バランスを保つて、除去剤(クリーム)の
乳化の安定化に寄与する。そして、この場合に高
級脂肪酸及び高級アルコールのいずれか一方のみ
を配合すると除去剤の乳化が不安定になり、数日
で分離を起こすし、展延性及び使用感が悪くな
る。除去剤の乳化安定性及び展延性等の使用感を
最良に保つ高級脂肪酸と高級アルコールの配合割
合は、除去剤全量に対して高級脂肪酸が2〜6重
量%、高級アルコールが5〜10重量%の範囲であ
る。 To explain each component of the beautiful nail enamel remover of the present invention, higher fatty acids and higher alcohols are:
Together, they enhance the spreadability of the remover (cream), improve the feeling of use of the remover, and maintain the emulsification balance of the remover as a whole, contributing to stabilization of the emulsification of the remover (cream). In this case, if only one of the higher fatty acid and higher alcohol is blended, the emulsification of the remover becomes unstable, separation occurs in a few days, and the spreadability and feeling of use become worse. The blending ratio of higher fatty acids and higher alcohols to maintain the best feel when using the remover, such as emulsion stability and spreadability, is 2 to 6% by weight of higher fatty acids and 5 to 10% by weight of higher alcohols based on the total amount of the remover. is within the range of
本発明において使用される高級脂肪酸として
は、炭素数が14〜22の飽和又は不飽和の一価脂肪
酸、たとえばミリスチン酸、パルミチン酸、ステ
アリン酸、オレイン酸及びベヘニン酸等があげら
れる。高級脂肪酸は1種類を使用してもよいし、
2種以上を併用してもよいし、さらには混合高級
脂肪酸を使用してもよい。 The higher fatty acids used in the present invention include saturated or unsaturated monovalent fatty acids having 14 to 22 carbon atoms, such as myristic acid, palmitic acid, stearic acid, oleic acid, and behenic acid. One type of higher fatty acid may be used,
Two or more types may be used in combination, or mixed higher fatty acids may be used.
本発明において使用される高級アルコールとし
ては、炭素数が14〜22の飽和又は不飽和の一価ア
ルコール、たとえばミリスチルアルコール、セチ
ルアルコール、ステアリルアルコール及びベヘニ
ルアルコール等があげられる。高級アルコールも
1種類を使用してもよいし、2種以上を併用して
もよいし、さらに混合高級アルコールを使用して
もよい。 Examples of the higher alcohol used in the present invention include saturated or unsaturated monohydric alcohols having 14 to 22 carbon atoms, such as myristyl alcohol, cetyl alcohol, stearyl alcohol, and behenyl alcohol. One type of higher alcohol may be used, two or more types may be used in combination, and a mixed higher alcohol may be used.
シヨ糖脂肪酸エステルは乳化剤として使用され
るものであり、除去剤全量に対して5〜8重量%
の割合で配合される。非イオン界面活性剤の量が
少なすぎると除去剤を安定なクリーム状に乳化さ
せることが困難になるし、多すぎても乳化バラン
スがくずれて、分離を起す原因となる。 Sucrose fatty acid ester is used as an emulsifier, and is 5 to 8% by weight based on the total amount of the remover.
It is blended in the proportion of If the amount of nonionic surfactant is too small, it will be difficult to emulsify the removing agent into a stable cream, and if it is too large, the emulsification balance will be disrupted, causing separation.
本発明におけるシヨ糖脂肪酸エステルとして
は、シヨ糖の種々の高級脂肪酸エステルがあげら
れ、そのエステルは単一脂肪酸のエステルであつ
てもよいし、数種の脂肪酸の混合エステルであつ
てもよい。天然油脂から製造された天然脂肪酸又
は天然脂肪酸から分離された脂肪酸を用いてエス
テル化したシヨ糖脂肪酸エステルは、通常、数種
の脂肪酸の混合エステルであることが多い。ま
た、そのシヨ糖脂肪酸エステルは、モノエステル
であつてもよいし、ジエステル以上のエステルで
あつてもよいし、モノエステルとジエステル以上
のエステルとの混合エステルであつてもよい。 Examples of the sucrose fatty acid ester in the present invention include various higher fatty acid esters of sucrose, and the ester may be an ester of a single fatty acid or a mixed ester of several types of fatty acids. Sucrose fatty acid esters esterified using natural fatty acids produced from natural oils or fatty acids separated from natural fatty acids are usually mixed esters of several types of fatty acids. Further, the sucrose fatty acid ester may be a monoester, a diester or higher ester, or a mixed ester of a monoester and a diester or higher ester.
炭素数10以上の脂肪酸エステルは美爪エナメル
を膨潤ないし溶解させて除去する作用の主役をな
すものである。この場合の炭素数10以上とは、脂
肪酸エステルを構成する脂肪酸の炭素数とアルコ
ールの炭素数の合計炭素数をいう。しかし、その
配合割合が多すぎても、少なすぎても乳化バラン
スがくずれるし、かつ少なすぎるとエナメル除去
効果が低下してくるので、除去剤全量に対して30
〜70重量%の範囲内で配合される。その脂肪酸エ
ステルとしては、たとえばアジピン酸ジイソブチ
ル、アジピン酸ジイソプロピル、及びアジピン酸
ジオクチルなどがあげられる。 Fatty acid esters having 10 or more carbon atoms play a major role in removing beautiful nail enamel by swelling or dissolving it. In this case, the number of carbon atoms of 10 or more refers to the total number of carbon atoms of the fatty acid and the alcohol that constitute the fatty acid ester. However, if the blending ratio is too high or too low, the emulsification balance will be disrupted, and if it is too low, the enamel removal effect will decrease.
It is blended within the range of ~70% by weight. Examples of the fatty acid ester include diisobutyl adipate, diisopropyl adipate, and dioctyl adipate.
グリコール類は湿潤剤ないし保湿剤としての作
用をするものであり、これを配合することにより
エナメルの除去の際に爪より水分が過度に除かれ
て、爪が光沢を失なつたり、白化したり、もろく
なつたりするのを有効に防止できるし、さらに除
去剤が皮ふに触れた場合に、皮ふより水分を過度
に除去して皮ふを荒らすのを防止できる。しか
し、グリコール類の割合が多くなりすぎるとエナ
メル除去作用が低下するので、除去剤全量に対し
て3〜8重量%の範囲で配合される。グリコール
類としては、たとえばポリエチレングリコール
(たとえば平均分子量300〜400)、プロピレングリ
コール、及び1,3−ブチレングリコール等があ
げられる。 Glycols act as humectants or moisturizers, and by adding them, excessive moisture is removed from the nails when removing enamel, causing the nails to lose their luster or become white. It can effectively prevent the skin from becoming brittle, and furthermore, when the remover comes into contact with the skin, it can prevent excessive removal of water from the skin and damage the skin. However, if the proportion of glycols is too high, the enamel removal effect will be reduced, so the amount of glycols is blended in the range of 3 to 8% by weight based on the total amount of the remover. Examples of glycols include polyethylene glycol (eg, average molecular weight 300 to 400), propylene glycol, and 1,3-butylene glycol.
パラオキシ安息香酸エステルは美爪エナメル除
去剤の防腐剤ないし保存剤として作用せしめるも
のであり、除去剤全量に対して0.2〜0.4重量%の
範囲で配合される。また、本発明の美爪エナメル
除去剤には、必要に応じてエチルアルコール、エ
チレングリコールモノメチルエーテル、エチレン
グリコールモノエチルエーテル、エチレングリコ
ールモノブチルエーテルなどが助溶剤として配合
される。エチルアルコール等の助溶剤の配合割合
は除去剤全量に対して0〜12重量%の範囲であ
る。エチルアルコールは、工業用の変性アルコー
ルとして使用するのがコスト面で好ましい。 Paraoxybenzoic acid ester acts as a preservative or preservative in the nail enamel remover, and is blended in an amount of 0.2 to 0.4% by weight based on the total amount of the nail enamel remover. Further, the beautiful nail enamel remover of the present invention may contain ethyl alcohol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, etc. as a co-solvent, if necessary. The proportion of the co-solvent such as ethyl alcohol is in the range of 0 to 12% by weight based on the total amount of the remover. Ethyl alcohol is preferably used as industrial denatured alcohol in terms of cost.
本発明の美爪エナメル除去剤には、以上述べた
各成分のほかに、残部として水が配合され、その
ために除去剤全体がクリーム状に乳化されたもの
となる。水は精製水を使用するのが望ましい。 In addition to the above-mentioned components, the beautiful nail enamel remover of the present invention contains water as the balance, so that the entire remover is emulsified into a creamy form. It is preferable to use purified water.
(実施例等)
以下に、実施例及び比較例をあげてさらに詳述
する。(Examples etc.) Below, Examples and Comparative Examples will be given and further explained in detail.
実施例 1
成分A (油相分)
ベヘニルアルコール 5.0g
ステアリン酸 2.0g
シヨ糖脂肪酸エステル(第一工業製薬社商品
名シユガーワツクスS−10E) 3.0g
アジピン酸ジイソプロピル 40.0g
パラオキシ安息香酸ブチル 0.1g
パラオキシ安息香酸メチル 0.1g
成分B (水相分)
精製水 30.8g
シヨ糖脂肪酸エステル(第一工業製薬社商品
名 DKエステルS−110) 3.0g
ポリオキシエチレングリコール(平均分子量
400) 6.0g
成分 C
エチルアルコール 10.0g
合計 100.0g
まず、成分Aの混合物を約80℃に加熱して溶解
させ、均一に混合した。Example 1 Component A (oil phase) Behenyl alcohol 5.0g Stearic acid 2.0g Sucrose fatty acid ester (Daiichi Kogyo Seiyaku Co., Ltd. trade name: Shugar Wax S-10E) 3.0g Diisopropyl adipate 40.0g Butyl paraoxybenzoate 0.1g Paraoxybenzoic acid Methyl 0.1g Component B (aqueous phase) Purified water 30.8g Sucrose fatty acid ester (Daiichi Kogyo Seiyaku product name DK Ester S-110) 3.0g Polyoxyethylene glycol (average molecular weight
400) 6.0g Component C Ethyl alcohol 10.0g Total 100.0g First, the mixture of component A was heated to about 80°C to dissolve it and mixed uniformly.
別に、成分Bの混合物を約80℃に加熱して溶解
させ、均一に混合したものに、前記の成分Aの均
一混合物を加えて、撹拌して乳化させ、さらにそ
の直後に成分Cを加えて、40℃に冷却するまで撹
拌して均一に混合して美爪エナメル除去剤を調製
した。 Separately, the mixture of component B was heated to about 80° C. to dissolve it, and the homogeneous mixture of component A was added to the homogeneous mixture, stirred and emulsified, and immediately after that, component C was added. A beautiful nail enamel remover was prepared by stirring until cooled to 40°C and mixing uniformly.
得られた美爪エナメル除去剤は、溶剤臭が少な
く、皮ふや粘膜に対する刺激もなく、エナメル除
去作用に優れており、かつ除去後の爪が光沢を有
し、白化が全く認められなかつた。また、この除
去剤は室温で3か月保存後も分離を起さなかつ
た。 The resulting beautiful nail enamel remover had little solvent odor, did not irritate the skin or mucous membranes, was excellent in enamel removal action, and had glossy nails with no whitening observed at all. Moreover, this remover did not cause separation even after being stored at room temperature for 3 months.
実施例 2
成分A (油相分)
ベヘニルアルコール 5.0g
ステアリン酸 5.0g
シヨ糖脂肪酸エステル(第一工業製薬社商品
名シユガーワツクスS−10E) 4.0g
アジピン酸ジイソプロピル 40.0g
パラオキシ安息香酸ブチル 0.2g
パラオキシ安息香酸メチル 0.2g
成分B (水相分)
シヨ糖脂肪酸エステル(第一工業製薬社商品
名DKエステルS−L18A) 3.0g
ポリエチレングリコール(分子量400)3.0g
精製水 29.6g
成分 C
エチルアルコール 10.0g
合計 100.0g
上記の成分A、成分B、及び成分Cを用い、実
施例1と同様にして美爪エナメル除去剤を調製し
た。得られた除去剤は、実施例で調製した除去剤
と同様に優れたものであつた。Example 2 Component A (oil phase) Behenyl alcohol 5.0g Stearic acid 5.0g Sucrose fatty acid ester (Daiichi Kogyo Seiyaku Co., Ltd. trade name: Shugar Wax S-10E) 4.0g Diisopropyl adipate 40.0g Butyl paraoxybenzoate 0.2g Paraoxybenzoic acid Methyl 0.2g Component B (aqueous phase) Sucrose fatty acid ester (Daiichi Kogyo Seiyaku Co., Ltd. trade name DK ester S-L18A) 3.0g Polyethylene glycol (molecular weight 400) 3.0g Purified water 29.6g Component C Ethyl alcohol 10.0g Total 100.0 g A beautiful nail enamel remover was prepared in the same manner as in Example 1 using the above Component A, Component B, and Component C. The obtained remover was as good as the remover prepared in the Examples.
上記の実施例で使用したシヨ糖脂肪酸エステル
の市販品の成分は下記のとおりである。 The components of the commercially available sucrose fatty acid ester used in the above examples are as follows.
シユガーワツクスS−10E:(第一工業製薬社
商品名)
シヨ糖のステアリン酸(70重量%)とパルミチ
ン酸(28重量%)とミリスチン酸(2重量%)
との混合エステル。水酸基価80〜130
DKエステルS−110:(第一工業製薬社商品
名)
シヨ糖のステアリン酸(70重量%)とパルミチ
ン酸(28重量%)とミリスチン酸(2重量%)
との混合エステル、モノエステル/(ジエステ
ル+トリエステル)モル比=50/50
DKエステルS−L18A:(第一工業製薬社商品
名)
シヨ糖のラウリン酸(68重量%)とミリスチン
酸(15重量%)とパルミチン酸(6重量%)と
カプリン酸(4重量%)とステアリン酸(3重
量%)とカプリン酸(2重量%)とオレイン酸
(2重量%)との混合エステル。モノエステ
ル/(ジエステル+トリエステル)モル比=
70/30
比較例 1
実施例2におけるベヘニルアルコールを全く使
用せずに、そのほかは実施例2と同様にして除去
剤を調整したところ、クリームの安定性が悪く、
数日後に分離を起した。また、この除去剤はエナ
メル除去効果も劣るものであつた。 Sugar Wax S-10E: (Daiichi Kogyo Seiyaku Co., Ltd. product name) Sugar stearic acid (70% by weight), palmitic acid (28% by weight), and myristic acid (2% by weight)
Mixed ester with. Hydroxyl value 80-130 DK Ester S-110: (Daiichi Kogyo Seiyaku Co., Ltd. product name) Stearic acid (70% by weight), palmitic acid (28% by weight), and myristic acid (2% by weight) of cane sugar
Mixed ester with monoester/(diester + triester) molar ratio = 50/50 DK Ester S-L18A: (Daiichi Kogyo Seiyaku Co., Ltd. product name) Lauric acid (68% by weight) and myristic acid (15% by weight) of cane sugar A mixed ester of palmitic acid (6% by weight), capric acid (4% by weight), stearic acid (3% by weight), capric acid (2% by weight) and oleic acid (2% by weight). Monoester/(diester + triester) molar ratio =
70/30 Comparative Example 1 When a remover was prepared in the same manner as in Example 2 without using any behenyl alcohol in Example 2, the stability of the cream was poor.
Separation occurred after a few days. Furthermore, this remover had poor enamel removal effect.
比較例 2
実施例2におけるステアリン酸を全く使用せず
に、そのほかは実施例2と同様にして除去剤を調
製したところ、使用感すなわちクリームの感触及
び展延性が悪く、かつ数日後にクリームが分離を
起した。また、エナメル除去効果も劣るものであ
つた。Comparative Example 2 When a remover was prepared in the same manner as in Example 2 except that the stearic acid in Example 2 was not used at all, the feeling of use, that is, the feel and spreadability of the cream was poor, and the cream deteriorated after a few days. Separation occurred. Furthermore, the enamel removal effect was also poor.
比較例 3
実施例2における成分A及び成分Bともに、シ
ヨ糖脂肪酸エステルを全く使用せずに、そのほか
は実施例2と同様にして除去剤を調製しようとし
たが、クリーム状にならず、除去剤としての使用
に耐えないものであつた。Comparative Example 3 For both Component A and Component B in Example 2, an attempt was made to prepare a remover in the same manner as in Example 2 without using any sucrose fatty acid ester, but the removal agent did not become cream-like and the removal was difficult. It was unsuitable for use as an agent.
比較例 4
実施例2におけるアジピン酸ジイソプロピルを
全く使用せずに、そのほかには実施例2と同様に
して除去剤を調製しようとしたが、得られたもの
はエナメル除去効果を全く示さなかつた。Comparative Example 4 An attempt was made to prepare a remover in the same manner as in Example 2 except that diisopropyl adipate in Example 2 was not used at all, but the product obtained did not exhibit any enamel removing effect.
比較例 5
実施例2におけるポリエチレングリコールを全
く使用せずに、そのほかは実施例2と同様にして
除去剤を調製したところ、得られた除去剤を用い
るとエナメル除去後の爪が水分が失なわれて光沢
のないものとなつてしまつた。Comparative Example 5 A remover was prepared in the same manner as in Example 2 except that the polyethylene glycol in Example 2 was not used at all, and when the resulting remover was used, the nails did not lose moisture after enamel removal. It has become dull and lackluster.
実施例 3
実施例1におけるベヘニルアルコールの代りに
セチルアルコールを使用し、そのほかは実施例1
と同様にして除去剤を調製したところ、実施例1
で得られたとほぼ同様の除去剤が得られた。Example 3 Cetyl alcohol was used instead of behenyl alcohol in Example 1, and the rest was as in Example 1.
A removing agent was prepared in the same manner as in Example 1.
A removing agent almost similar to that obtained was obtained.
実施例 4
実施例1におけるステアリン酸の代りにパルミ
チン酸を使用し、そのほかは実施例1と同様にし
て除去剤を調製したところ、実施例1で得られた
とほぼ同様の除去剤が得られた。Example 4 A remover was prepared in the same manner as in Example 1 except that palmitic acid was used instead of stearic acid in Example 1, and a remover almost the same as that obtained in Example 1 was obtained. .
実施例 5
実施例1におけるアジピン酸ジイソプロピルの
代りにアジピン酸ジオクチルを使用し、そのほか
は実施例1と同様にして除去剤を調製したとこ
ろ、実施例1で得られたとほぼ同様の除去剤が得
られた。Example 5 A removing agent was prepared in the same manner as in Example 1 except that dioctyl adipate was used in place of diisopropyl adipate in Example 1, and a removing agent almost the same as that obtained in Example 1 was obtained. It was done.
実施例 6
実施例1におけるポリエチレングリコールの代
りにプロピレングリコールを使用し、そのほかは
実施例1と同様にして除去剤を調製したところ、
実施例1で得られたとほぼ同様の除去剤が得られ
た。Example 6 A removing agent was prepared in the same manner as in Example 1 except that propylene glycol was used instead of polyethylene glycol in Example 1.
A removing agent substantially similar to that obtained in Example 1 was obtained.
Claims (1)
〜10重量%、シヨ糖脂肪酸エステル5〜8重量
%、炭素数が10以上の脂肪酸エステル30〜70重量
%、グリコール類3〜8重量%、パラオキシ安息
香酸エステル0.2〜0.4重量%、残部が水及び必要
に応じて添加する助溶剤よりなる美爪エナメル除
去剤。1 Higher fatty acids 2-6% by weight, higher alcohols 5
~10% by weight, 5-8% by weight of sucrose fatty acid ester, 30-70% by weight of fatty acid ester having 10 or more carbon atoms, 3-8% by weight of glycols, 0.2-0.4% by weight of paraoxybenzoic acid ester, the balance being water A beautiful nail enamel remover consisting of a co-solvent and a co-solvent added as necessary.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29325485A JPS62155206A (en) | 1985-12-27 | 1985-12-27 | Manicure enamel remover |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29325485A JPS62155206A (en) | 1985-12-27 | 1985-12-27 | Manicure enamel remover |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62155206A JPS62155206A (en) | 1987-07-10 |
JPS6324969B2 true JPS6324969B2 (en) | 1988-05-23 |
Family
ID=17792442
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP29325485A Granted JPS62155206A (en) | 1985-12-27 | 1985-12-27 | Manicure enamel remover |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62155206A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0580174U (en) * | 1992-03-31 | 1993-10-29 | 株式会社三協精機製作所 | Coupling member |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2696222B2 (en) * | 1988-05-07 | 1998-01-14 | 株式会社資生堂 | Emulsified enamel remover |
JP3005599B2 (en) * | 1991-07-31 | 2000-01-31 | 株式会社大阪造船所 | Cleaning agent |
JP5291365B2 (en) * | 2008-03-18 | 2013-09-18 | 株式会社ナリス化粧品 | Keratin condition improving agent |
WO2015152211A1 (en) * | 2014-03-31 | 2015-10-08 | 富士フイルム株式会社 | Artificial nail removal liquid, artificial nail removal method, and nail art kit |
-
1985
- 1985-12-27 JP JP29325485A patent/JPS62155206A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0580174U (en) * | 1992-03-31 | 1993-10-29 | 株式会社三協精機製作所 | Coupling member |
Also Published As
Publication number | Publication date |
---|---|
JPS62155206A (en) | 1987-07-10 |
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