JPH0278606A - Manicure - Google Patents
ManicureInfo
- Publication number
- JPH0278606A JPH0278606A JP23122788A JP23122788A JPH0278606A JP H0278606 A JPH0278606 A JP H0278606A JP 23122788 A JP23122788 A JP 23122788A JP 23122788 A JP23122788 A JP 23122788A JP H0278606 A JPH0278606 A JP H0278606A
- Authority
- JP
- Japan
- Prior art keywords
- nitrocellulose
- ethanol
- manicure
- film
- lower alcohol
- 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
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 60
- 229920001220 nitrocellulos Polymers 0.000 claims abstract description 44
- 239000000020 Nitrocellulose Substances 0.000 claims abstract description 42
- 230000003796 beauty Effects 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000002904 solvent Substances 0.000 abstract description 31
- 230000000694 effects Effects 0.000 abstract description 19
- 239000003795 chemical substances by application Substances 0.000 abstract description 10
- 229920005989 resin Polymers 0.000 abstract description 10
- 239000011347 resin Substances 0.000 abstract description 10
- 229920002678 cellulose Polymers 0.000 abstract description 7
- 239000001913 cellulose Substances 0.000 abstract description 7
- 239000004014 plasticizer Substances 0.000 abstract description 6
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical group O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 abstract description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 4
- 239000002253 acid Substances 0.000 abstract description 2
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Chemical group OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 abstract 1
- 239000000470 constituent Substances 0.000 abstract 1
- 239000002932 luster Substances 0.000 abstract 1
- 230000002459 sustained effect Effects 0.000 abstract 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 8
- 150000002576 ketones Chemical class 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 230000002087 whitening effect Effects 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 5
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 5
- 210000003298 dental enamel Anatomy 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 150000002170 ethers Chemical class 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 238000005336 cracking Methods 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 239000002075 main ingredient Substances 0.000 description 4
- 238000006467 substitution reaction Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 150000001242 acetic acid derivatives Chemical class 0.000 description 2
- -1 alkyl vinyl ether Chemical compound 0.000 description 2
- 230000001680 brushing effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 230000003203 everyday effect Effects 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 230000005923 long-lasting effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- YCMLQMDWSXFTIF-UHFFFAOYSA-N 2-methylbenzenesulfonimidic acid Chemical compound CC1=CC=CC=C1S(N)(=O)=O YCMLQMDWSXFTIF-UHFFFAOYSA-N 0.000 description 1
- QZCLKYGREBVARF-UHFFFAOYSA-N Acetyl tributyl citrate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 description 1
- MRABAEUHTLLEML-UHFFFAOYSA-N Butyl lactate Chemical compound CCCCOC(=O)C(C)O MRABAEUHTLLEML-UHFFFAOYSA-N 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 101000863770 Homo sapiens DNA ligase 1 Proteins 0.000 description 1
- 101000619640 Homo sapiens Leucine-rich repeats and immunoglobulin-like domains protein 1 Proteins 0.000 description 1
- 102100022170 Leucine-rich repeats and immunoglobulin-like domains protein 1 Human genes 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
- 239000004677 Nylon Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- QXNIBPDSSDVBQP-UHFFFAOYSA-N acetic acid;2-methylpropanoic acid Chemical compound CC(O)=O.CC(C)C(O)=O QXNIBPDSSDVBQP-UHFFFAOYSA-N 0.000 description 1
- 229920006222 acrylic ester polymer Polymers 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000001191 butyl (2R)-2-hydroxypropanoate Substances 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000002354 daily effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 231100000016 inhalation toxicity Toxicity 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229920003146 methacrylic ester copolymer Polymers 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、光沢、硬度、屈曲性、耐水性、メイクアップ
効果の持続性等の特性に優れており、かつ長時間使用し
ても人体に安全な美爪料を提供するものである。Detailed Description of the Invention (Field of Industrial Application) The present invention has excellent properties such as gloss, hardness, flexibility, water resistance, and long-lasting make-up effect, and even after long-term use, It provides safe nail beauty products for people.
(従来の技術と発明が解決しようとする課題)従来爪に
塗布し、艶を与えて爪の美しさを強調するネイルエナメ
ルを中心とする美爪料は、通常皮膜形成主剤としてH型
ニトロセルロースを用い、可塑、荘Iべ構脂類を適宜配
合して、揮発成分である溶剤に均一に溶解した系に、必
要に応じて色材等を分散または溶解して成る。このうち
揮発性溶剤は、酢酸エチル、酢酸ブチル、乳酸ブチル等
のエステル類、メチルエチルケトン、メチルイソブチル
ケトン等のケトン類、エチレングリコールモノエチルエ
ーテル等のエーテル類、エタノール、イソプロピルアル
コール、n−ブチルアルコール等のアルコール類、トル
エン、キシレン等の芳香族系炭化水素類が用いられてい
る。(Problems to be solved by conventional techniques and inventions) Conventional nail beauty products, mainly nail enamels that are applied to nails to give shine and emphasize the beauty of the nails, usually use H-type nitrocellulose as the film-forming main agent. A coloring material and the like are dispersed or dissolved as necessary in a system in which plasticizers and structural fats are appropriately blended and dissolved uniformly in a solvent as a volatile component. Volatile solvents include esters such as ethyl acetate, butyl acetate, butyl lactate, ketones such as methyl ethyl ketone and methyl isobutyl ketone, ethers such as ethylene glycol monoethyl ether, ethanol, isopropyl alcohol, n-butyl alcohol, etc. alcohols, and aromatic hydrocarbons such as toluene and xylene.
これらはニトロセルロースに対する溶解力に応じて三つ
の群に分類される。それは(11真溶剤又は活性溶剤と
呼ばれるニトロセルロースに対する溶解力のある群、(
2)助溶剤又は潜伏性溶剤と呼ばれるそれ自体では、ニ
トロセルロースに対する溶解力はないが、真溶剤と組み
合わせることによって、溶解力を増加させ、溶液の粘度
を下げる群、(3)希釈剤と呼ばれるニトロセルロース
に対する熔解力が全くなく、溶液の粘度を安定させ、他
の樹脂の熔解に関与する群である。前述の揮発性溶剤の
中では、エステル類、ケトン類、エーテル類は、ニトロ
セルロースの真溶剤に分類され、従来のニトロセルロー
スを皮膜形成主剤として用いた美爪料においては、少な
くともそのうちの一種を配合する事が不可欠であった。These are classified into three groups depending on their ability to dissolve nitrocellulose. It is a group of solvents called true or active solvents that have the ability to dissolve nitrocellulose (11).
2) A group called co-solvents or latent solvents, which do not have the ability to dissolve nitrocellulose by themselves, but when combined with a true solvent, increase the solvency and reduce the viscosity of the solution; (3) A group called diluents. This group has no ability to dissolve nitrocellulose, stabilizes the viscosity of the solution, and is involved in the melting of other resins. Among the volatile solvents mentioned above, esters, ketones, and ethers are classified as true solvents for nitrocellulose, and at least one of them is used in conventional nail polishes that use nitrocellulose as a film-forming main ingredient. It was essential to mix them together.
また、アルコール類は助溶剤、芳香族系炭化水素類は希
釈剤に分類され、それぞれ単独または二種以上を組み合
わせてもニトロセルロースを溶解させることができない
とされるものである。Further, alcohols are classified as co-solvents, and aromatic hydrocarbons are classified as diluents, and it is said that they cannot dissolve nitrocellulose either alone or in combination of two or more.
一方、これらの揮発性溶剤の中で、エステル類。On the other hand, among these volatile solvents, esters.
ケトン類、エーテル類、芳香族炭化水素類は、何れも人
体に対する吸引毒性が強く、また接触することによって
、爪や回りの皮膚に対して悪影響を与える事から、これ
らの溶剤使用は問題視されていた。にもかかわらず、ニ
トロセルロースの真溶剤であるエステル類、ケトン類、
エーテル類からなる群から選ばれる少なくとも一種を配
合しなければ、ニトロセルロースを皮膜形成主剤とする
美爪料を提供することができず、今だ満足し得る解決策
を見い出していなかった。また、従来のニトロセルロー
スを皮膜形成主剤とした美爪料を爪から除去するエナメ
ルリムーバーについては、同様にニトロセルロースの真
溶剤を主成分として用い、ケトン類や酢酸エステル類を
多量に配合したものであった。この為従来のエナメルリ
ムーバーは、吸引毒性が強いと同時に、ケトン類や酢酸
エステル類を主成分とする揮発性溶剤の脱脂作用、脱水
作用により、爪の水分、油分を過度に奪い取る為に、爪
の表面を傷め、爪を白化させたり割れやすくするという
欠点があった。Ketones, ethers, and aromatic hydrocarbons are all highly toxic to the human body when inhaled, and contact with them can have an adverse effect on the nails and surrounding skin, so the use of these solvents is considered problematic. was. Nevertheless, esters, ketones, which are true solvents for nitrocellulose,
Unless at least one selected from the group consisting of ethers is incorporated, it is not possible to provide a nail beauty product that uses nitrocellulose as a film-forming main ingredient, and a satisfactory solution has not yet been found. In addition, conventional enamel removers that use nitrocellulose as a film-forming agent to remove nail polish from nails are similar to enamel removers that use nitrocellulose as a true solvent as the main ingredient and contain large amounts of ketones and acetate esters. Met. For this reason, conventional enamel removers have strong inhalation toxicity, and at the same time remove excessive moisture and oil from the nails due to the degreasing and dehydrating effects of volatile solvents mainly composed of ketones and acetate esters. It has the disadvantage that it damages the surface of nails and makes nails whiter and more likely to break.
一方、こうしたエステル類、ケトン類、エーテル類、芳
香族系炭化水素類を用いないで、美爪料を提供する試み
もなされているが、いずれも皮膜形成主剤としてニトロ
セルロースを用いていない為に耐水性、メイクアンプ効
果の持続性等において満足し得る皮膜を形成させる事が
できなかった。On the other hand, attempts have been made to provide nail polishes without using these esters, ketones, ethers, and aromatic hydrocarbons, but none of them use nitrocellulose as the main film-forming agent. It was not possible to form a film that was satisfactory in terms of water resistance, durability of the make-up effect, etc.
即ち、特開昭54−20143公報には、アルキルビニ
ルエーテル/無水マレイン酸共重合体のハーフエステル
を、特開昭57−50908公iにはポリビニルアセタ
ール低級ジアルキルアミノアセテートをそれぞれ皮膜形
成主剤とし、揮発性溶剤として脂肪族低級アルコールを
配合した美爪料が開示されているが、いずれも形成され
る皮膜の耐水性、メイクアップ効果の持続性という点に
おいて、満足し得るものではなかった。That is, in JP-A-54-20143, a half ester of alkyl vinyl ether/maleic anhydride copolymer is used as a film-forming main agent, and in JP-A-57-50,908, polyvinyl acetal lower dialkylamino acetate is used as a film-forming main agent and volatilized. Nail cosmetics containing an aliphatic lower alcohol as a solvent have been disclosed, but none of them were satisfactory in terms of the water resistance of the film formed and the sustainability of the makeup effect.
て鋭意研究を重ねた結果、L型ニトロセルロースを皮膜
形成主剤として用い、エタノールを80%以上含む炭素
数2〜4の低級アルコールからなる揮発性溶剤に溶解さ
せた後、必要に応じてエタノール可溶性の可塑剤、樹脂
類を適宜配合して得た美爪料が、人体に対して安全性が
高く、従来のエステル系、ケトン系、エーテル系、芳香
族炭化水素系の揮発性溶剤を含有する美爪料と同様に使
用特性に優れている事を見い出し本発明を完成するに至
った。As a result of extensive research, we discovered that L-type nitrocellulose was used as the main agent for film formation, and after it was dissolved in a volatile solvent consisting of a lower alcohol with 2 to 4 carbon atoms containing 80% or more of ethanol, ethanol-soluble Nail beauty products obtained by appropriately blending plasticizers and resins are highly safe for the human body and contain conventional ester-based, ketone-based, ether-based, and aromatic hydrocarbon-based volatile solvents. The present invention was completed after discovering that it has excellent properties in use, similar to nail beauty products.
本発明はL型ニトロセルロースと炭素数2〜4の低級ア
ルコールとを主要構成成分とする美爪料に於いて、低級
アルコール中のエタノール含有量が80重量%以上であ
ることを特徴とする美爪料である。The present invention provides a nail beauty product containing L-type nitrocellulose and a lower alcohol having 2 to 4 carbon atoms as main components, wherein the ethanol content in the lower alcohol is 80% by weight or more. It is a nail polish.
以下本発明の構成について詳説する。The configuration of the present invention will be explained in detail below.
本発明に使用するニトロセルロースは公知の物質であっ
て、天然セルロースを混酸で硝酸エステル化しセルロー
ス中の水酸基(−OH)を硝酸基(Nov>に置換する
ことによって得られるセルロース誘導体であり、セルロ
ースの無水グルコビラノース基の六員環中の3個の水酸
基のうち、いくつを硝酸基に置換するかによって、その
性質を変える事ができる。従来広く用いられているH型
ニトロセルロースは平均置換度2.1〜2.3(7)範
囲にあるものであるが、1.9〜2.1の平均置換度で
置換することによりL型ニトロセルロースを得ることが
できる。なお、本明細書中のし型及びH型は、JIS
K6703−75によって規定された窒素骨による分
類を示す、即ち、L型ニトロ分11.5%以上12.2
%以下のセルロースである。Nitrocellulose used in the present invention is a known substance, and is a cellulose derivative obtained by esterifying natural cellulose with a mixed acid and replacing the hydroxyl group (-OH) in cellulose with a nitric acid group (Nov>). Its properties can be changed depending on how many of the three hydroxyl groups in the six-membered ring of the anhydrous glucobylanose group are substituted with nitric acid groups.H-type nitrocellulose, which has been widely used in the past, has an average substitution Although the degree of substitution is in the range of 2.1 to 2.3 (7), L-type nitrocellulose can be obtained by substitution with an average degree of substitution of 1.9 to 2.1. The middle diamond shape and H shape are JIS
Shows the classification according to nitrogen bone defined by K6703-75, i.e. L-type nitro content 11.5% or more 12.2
% or less of cellulose.
窒素含量が1165%以上であるニトロセルロースは、
エタノール、゛n−プロピルアルコール、イソプロピル
アルコール、n−7”チルアルコール。Nitrocellulose with a nitrogen content of 1165% or more is
Ethanol, n-propyl alcohol, isopropyl alcohol, n-7'' alcohol.
イソブチルアルコールの単独あるいは二種以上を組み合
わせた場合のいずれにも透明に溶解させることができず
、白濁、ゲル化あるいは沈澱を生じ本発明に用いる事は
できない、窒素含量が10.7%未満であるニトロセル
ロースも、同様の理由から好ましくない。When the nitrogen content is less than 10.7%, it cannot be dissolved transparently in isobutyl alcohol alone or in combination of two or more types, and it causes cloudiness, gelation, or precipitation, and cannot be used in the present invention. Certain nitrocelluloses are also undesirable for similar reasons.
本発明におけるL型ニトロセルロースは、通常市販のも
のを用いる事ができ、重合度は特に限定されないが通常
40〜450程度である。市販品としては、例えば、硝
化綿LICI/8.LIG1/4.LICI/2 (以
上旭化成工業製)FQタイプ硝化綿SSI/8.SSI
/4,331/2,5S20 (以上ダイセル化学工業
製)等を挙げる事ができるが本発明がこれらの製品だけ
に限定されるわけではない。As the L-type nitrocellulose in the present invention, commercially available products can be used, and the degree of polymerization is not particularly limited, but is usually about 40 to 450. Commercially available products include, for example, nitrified cotton LICI/8. LIG1/4. LICI/2 (manufactured by Asahi Kasei Industries) FQ type nitrified cotton SSI/8. SSI
/4, 331/2, 5S20 (manufactured by Daicel Chemical Industries, Ltd.), but the present invention is not limited to these products.
本発明におけるニトロセルロース(乾燥純分)の配合量
は美爪料全量に対して3〜2g重量%の範囲が望ましく
、爪に塗布が容易な粘度を保ち、かつメイクアップ効果
の高い厚みを持った皮膜を形成する美爪料を得る為には
5〜20重量%の範囲が特に好ましい、配合量3重量%
未満では、爪にメイクアップ効果を与えるのに充分な厚
みの皮膜を形成することができず、25重量%を超えて
配合すると揮発性溶剤に対する溶解度を越える為、ニト
ロセルロースの沈澱を生じたり白濁、ゲル化等の現象を
引き起こす為に好ましくない。The amount of nitrocellulose (dry pure content) in the present invention is preferably in the range of 3 to 2 g% by weight based on the total amount of the nail beauty agent, and has a viscosity that makes it easy to apply to the nails and a thickness that provides a high makeup effect. In order to obtain a nail polish that forms a beautiful film, the range of 5 to 20% by weight is particularly preferable, and the blending amount is 3% by weight.
If it is less than 25% by weight, it will not be possible to form a film of sufficient thickness to give a makeup effect to the nails, and if it is more than 25% by weight, the solubility in volatile solvents will be exceeded, resulting in nitrocellulose precipitation or clouding. , which is undesirable because it causes phenomena such as gelation.
本発明に用いる揮発性溶剤はエタノールを80重量%以
上含有する炭素数2〜4の低級アルコールから成るが、
人体への安全性を考えると、エタノールを単独で用いる
のが最も好ましい。The volatile solvent used in the present invention consists of a lower alcohol having 2 to 4 carbon atoms containing 80% by weight or more of ethanol,
Considering safety to the human body, it is most preferable to use ethanol alone.
しかし、エタノールを単独で揮発性溶剤として用いると
、乾燥速度が速すぎる為に、モイスチャーブラッシング
(蒸発熱によって空気中の水分が凝集して、皮膜が白化
する現象)やオレンジピール(溶剤の急速な蒸発を原因
の一つとして生じる皮膜表面の凹凸現象)が発生する場
合には、より高沸点の脂肪族低級アルコールであるイソ
プロピルアルコール、n−ブタノール等を配合して蒸発
速度を調整することができる。ただし、この場合、エタ
ノール以外の脂肪族低級アルコールの配合量は、揮発性
溶剤全量に対して20重量%が限度であり、これを超え
て配合するとニトロセルロースを透明に溶解させること
ができず、均一で強靭な皮膜を形成できない。均一で、
硬<、透明度が高い皮膜を形成する為には、エタノール
以外の脂肪族低級アルコールの配合量は10重量%未満
であることが特に好ましい。However, when ethanol is used alone as a volatile solvent, the drying speed is too fast, resulting in moisture brushing (a phenomenon in which moisture in the air condenses due to heat of evaporation and whitening of the film) and orange peel (a phenomenon in which the film whitens due to the condensation of moisture in the air due to the heat of evaporation). If unevenness on the film surface occurs due to evaporation, the evaporation rate can be adjusted by adding isopropyl alcohol, n-butanol, etc., which are aliphatic lower alcohols with higher boiling points. . However, in this case, the amount of aliphatic lower alcohol other than ethanol is limited to 20% by weight based on the total amount of volatile solvent, and if it is added in excess of this, nitrocellulose cannot be dissolved transparently. Unable to form a uniform and strong film. uniform,
In order to form a film with high hardness and transparency, it is particularly preferable that the amount of the aliphatic lower alcohol other than ethanol is less than 10% by weight.
一方ニトロセルロースは、乾燥状態では発火し易く、発
火すると、非常に急速に燃焼し、危険である事から市販
品は通常、全量に対して30重量%のイソプロピルアル
コールで湿潤させた状態で提供されている。この為、市
販のニトロセルロースをそのまま配合するとニトロセル
ロース(乾燥)70重量%に対して30重量%のイソプ
ロピルアルコールも同時に混入する事になる。On the other hand, nitrocellulose is easily ignitable in a dry state, and when ignited, it burns very rapidly and is dangerous, so commercially available products are usually provided in a state moistened with 30% by weight of isopropyl alcohol. ing. Therefore, if commercially available nitrocellulose is blended as is, 30% by weight of isopropyl alcohol will also be mixed in with 70% by weight of nitrocellulose (dry).
本発明の美爪料においては、エタノールを主成分とした
揮発性溶剤中におけるエタノール以外の脂肪族低級アル
コールの配合量が増大するにしたかって、揮発性溶剤の
ニトロセルロースに対する溶解力が低下する為に、多量
のニトロセルロースを溶解する場合には、できるだけエ
タノール以外の脂肪族低級アルコールの配合量は、モイ
スチャーブラッシングやオレンジピールを防止できる範
囲で少なくする事が望ましい、この為、市販のニトロセ
ルロースを湿潤させているイソプロピルアルコールを乾
燥等の方法によって、あらかじめ15重置%以下にして
おく事が望ましい、エタノール以外に揮発性、溶剤を全
く含有しない美爪料を得る方法としては、極めて注意深
(、危険のない方法によってニトロセルロースを乾燥さ
せてイソプロピルアルコールを除去した後、すぐにエタ
ノールに溶解して用いる方法が挙げられる。In the nail polish of the present invention, as the amount of aliphatic lower alcohol other than ethanol increases in the volatile solvent mainly composed of ethanol, the dissolving power of the volatile solvent for nitrocellulose decreases. When dissolving a large amount of nitrocellulose, it is desirable to reduce the amount of aliphatic lower alcohol other than ethanol to the extent that can prevent moisture brushing and orange peel. It is desirable to reduce the moistening isopropyl alcohol to 15% by weight or less by drying or other methods.In order to obtain a beautiful nail polish that does not contain any volatile or solvent other than ethanol, be extremely careful ( Another method is to dry nitrocellulose to remove isopropyl alcohol by a non-hazardous method and then immediately dissolve it in ethanol.
従来ニトロセルロースを皮膜形成主剤として用いる美爪
料には、皮膜のヒビ割れを防止する為に可塑剤が用いら
れているが、本発明においても、通常ニトロセルロース
の可塑剤として用いられているもののうち、エタノール
に溶解するか、均一に混和するものであれば配合するこ
とは何ら問題かない。本発明に配合し得る可塑剤として
は、カンフル、フタル酸ジブチル、クエン酸アセチルト
リブチル等が挙げられる。Conventionally, nail polishes that use nitrocellulose as a film-forming main ingredient have used plasticizers to prevent the film from cracking. Of these, there is no problem in blending them as long as they dissolve in ethanol or are uniformly miscible with it. Examples of plasticizers that can be incorporated in the present invention include camphor, dibutyl phthalate, acetyltributyl citrate, and the like.
また、従来ニトロセルロースを皮膜形成主剤として用い
る美爪料には、ニトロセルロース皮膜の光沢性、収縮性
、密着性等を改良する為に樹脂類が配合されているが、
本発明における美爪料においても、エタノールに溶解し
ニトロセルロースと+I N性のあるものであれば配合
することができる。In addition, conventional nail polishes that use nitrocellulose as the main film-forming agent contain resins to improve the gloss, shrinkage, adhesion, etc. of the nitrocellulose film.
In the nail beauty preparation of the present invention, any material that dissolves in ethanol and has +IN properties with nitrocellulose can be blended.
本発明に配合し得る樹脂類としては、シェラツク。Examples of resins that can be blended in the present invention include shellac.
、ダンマー、トルエンスルホンアミドホルムアルデヒド
樹脂、ポリビニルブチラール、アクリル酸エステル/メ
タクリル酸エステル共重合体、アクリル酸/スチレン共
重合体、アルコール溶性゛ロジン変性マレイン酸エステ
ル樹脂、ヒマシ油変性シクロヘキサン系ポリエステル樹
脂、シェークローズアセテートイソブチレート等を挙げ
ることができる。, Danmar, toluenesulfonamide formaldehyde resin, polyvinyl butyral, acrylic ester/methacrylic ester copolymer, acrylic acid/styrene copolymer, alcohol-soluble rosin-modified maleic ester resin, castor oil-modified cyclohexane polyester resin, shake Examples include rose acetate isobutyrate.
なお、本発明に用いる炭素数2〜4の低重アルコールか
らなる揮発性溶剤の配合量は、ニトロセルロース、樹脂
類、可塑剤、顔料等の配合量によって決まるが、通常、
美爪料全量に対して60〜90重量%が望ましい、60
重量%未満では、相対的にニトロセルロース、樹脂類、
I料等の配合量が多くなる為に、粘度が高くなり、爪に
塗布することが困難となる。90重量%を越えて配合す
ると、相対的にニトロセルロースや樹脂類の配合量が少
なくなる為に、爪にメイクアップ効果を与えるのに充分
な厚みの皮膜を形成することができない。The amount of the volatile solvent consisting of a low heavy alcohol having 2 to 4 carbon atoms used in the present invention is determined by the amount of nitrocellulose, resins, plasticizers, pigments, etc., but usually,
Desirably 60 to 90% by weight based on the total amount of nail polish, 60
Less than % by weight, relatively nitrocellulose, resins,
Since the amount of I ingredients etc. increases, the viscosity increases, making it difficult to apply to the nails. If it exceeds 90% by weight, the amount of nitrocellulose and resin to be blended will be relatively small, making it impossible to form a film of sufficient thickness to provide a makeup effect to the nails.
(実施例)
以下実施例によって本発明を更に詳細に説明するが、本
発明の技術範囲はこれらの実施例によって限定されるも
のではない。配合量は重量%である。ニトロセルロース
の配合量は、乾燥純分で示しである。(Examples) The present invention will be explained in more detail with reference to Examples below, but the technical scope of the present invention is not limited by these Examples. The blending amount is in weight%. The amount of nitrocellulose blended is shown in dry pure content.
実施例に示した美爪料の光沢、硬度、屈曲性。Gloss, hardness, and flexibility of the nail polish shown in Examples.
耐水性、メイクアップ効果の持続性、爪の損傷程度の試
験法は以下の通りである。The test methods for water resistance, durability of makeup effect, and degree of nail damage are as follows.
ill 光沢
ガラス板に80μの厚さで均一に試料を塗布し、30℃
にて24時間乾燥後グロスメーターを用いて入射角30
℃で反射率を測定した0反射率90%以上のものを0.
90〜70%のものを△、70%以下のものを×とした
。Apply the sample uniformly to a thickness of 80μ on a glossy glass plate and heat at 30°C.
After drying for 24 hours at
Reflectance measured at ℃ 0 reflectance of 90% or more is 0.
90 to 70% was rated △, and 70% or less was rated ×.
(2) 硬度
ガラス板に80μの厚さで均一に試料を塗布し、30℃
にて24時間乾燥後JI35400「塗料−船試験法」
に準じて鉛筆硬度計にて測定した。荷重300g角度4
5℃の条件で皮膜に傷を生じさせ得る鉛筆硬度が2H以
上のものをO,H〜HBのものをΔ、B以下のものを×
とした。(2) Apply the sample uniformly to a hardness glass plate with a thickness of 80μ, and heat it at 30°C.
After drying for 24 hours, JI35400 "Paint - Ship Testing Method"
The hardness was measured using a pencil hardness meter according to . Load 300g Angle 4
Those with a pencil hardness of 2H or higher that can cause scratches on the film at 5°C are O, those between H and HB are Δ, and those below B are ×.
And so.
(3) 屈曲性
80μの厚さに試料を塗布したナイロン板を、塗布後1
日毎に1回180”折り曲げ、亀裂が生じるまでの期間
(日数)を測定した。5日以上を0.2〜4日をΔ、1
日以下を×とした。(3) A nylon plate coated with the sample to a thickness of 80μ in flexibility was
It was bent 180" once every day and the period (number of days) until cracking was measured. 0.2 to 4 days for 5 days or more, Δ, 1
Days or less were marked as ×.
(4) 耐水性
ガラス仮に80μの厚さで均一に試料を塗布し、30℃
にて24時間乾燥後、そのガラス板を40℃の水中に1
時間浸漬して白化、膨潤。(4) Water-resistant glass. Apply a sample uniformly to a thickness of 80μ and heat it at 30°C.
After drying for 24 hours, the glass plate was placed in water at 40℃ for 1 hour.
Whitening and swelling after soaking for a while.
剥離の程度を肉眼観察した。全く変化のないものをOl
やや白化するものを△、白化が著しいものや、皮膜が膨
潤してガラス板から剥離するものを×とした。The degree of peeling was visually observed. Ol something that doesn't change at all
A sample with slight whitening was graded △, and a sample with significant whitening or a coating that swelled and peeled off from the glass plate was graded x.
(5) メイクアップ効果の持続性
10名の女性被験者の爪に試料を塗布し、−日ごとに皮
膜の光沢、剥離2表面のキズを観察し、試料のメイクア
ップ効果が日常生活の中で何日持続するかを判定した。(5) Sustainability of make-up effect Samples were applied to the nails of 10 female subjects, and the gloss of the film and scratches on the peeled surface were observed every day to see if the make-up effect of the sample would be maintained in daily life. Determine how many days it will last.
3日以上効果が持続した被験者の数が8名以上のものを
0.3〜7名のものをΔ、2名以下のものを×とした。If the effect lasted for 3 days or more in 8 or more subjects, 0.3 to 7 subjects was rated Δ, and if it was 2 or fewer subjects, it was rated ×.
(6) 爪の損傷程度
10名の女性海被験者に試料を3力月間使用させ、爪の
白化、ヒビ割れ等の変化を観察した。(6) Degree of damage to nails Ten female test subjects used the sample for three months, and changes such as whitening and cracking of the nails were observed.
全員が爪の変化を惑しなかったものを○、爪の変化を感
じた被験者が1名以上いたものを×とした。If none of the subjects were confused by the change in the nails, it was marked as ○, and if one or more subjects felt that the nails had changed, it was marked as ×.
なお、エナメルリムーバーは、比較例のH型ニトロセル
ロースを試料としたものは市販品を、その他の試料の場
合はエタノールを用いた。As for the enamel remover, a commercially available product was used for the H-type nitrocellulose sample of the comparative example, and ethanol was used for the other samples.
(製法) 処方を第1表に示す。(Manufacturing method) The prescription is shown in Table 1.
■〜■を均一に混合した後、■〜■及び@〜@を加えて
溶解する0次いで[相]、■及びOを加えて均一に混合
して美爪料を得た。After uniformly mixing ① to ①, ① to ① and @ to @ were added and dissolved. Next, [phase], ① and O were added and mixed uniformly to obtain a nail polish.
(特性)
実施例1〜5、比較例1〜4の美爪料の各項目の評価結
果を第2表に示す。(Characteristics) Table 2 shows the evaluation results for each item of the nail beauty products of Examples 1 to 5 and Comparative Examples 1 to 4.
実施例1〜5は、光沢、硬度、屈曲性、耐水性。Examples 1 to 5 are gloss, hardness, flexibility, and water resistance.
メイクアップ効果の持続性の各項目に優れた製品特性を
示し、かつ3ケ月間連続して使用しても爪に影響を与え
ない安全性の高い優れたものであった。The product exhibited excellent product characteristics in terms of durability of makeup effect, and was highly safe and did not affect the nails even after continuous use for 3 months.
比較例Iは、ニトロセルロースが揮発性溶剤に完全に溶
解せずに沈澱を生じた為に美爪料を得ることができず評
価することができなかった。In Comparative Example I, the nitrocellulose was not completely dissolved in the volatile solvent and precipitated, so that a nail beauty product could not be obtained and could not be evaluated.
比較例2は、溶剤に酢酸エチル9.酢酸ブチル。Comparative Example 2 uses 9.9% ethyl acetate as the solvent. Butyl acetate.
トルエンを用いており、光沢、硬度、屈曲性、耐水性、
メイクアップ効果の持続性において優れたものであるが
、3ケ月間連続して使用すると、爪の白化やヒビ割れを
惑じる被験者が生じ、満足し得るものでなかった。Using toluene, it has gloss, hardness, flexibility, water resistance,
Although this product has an excellent long-lasting makeup effect, when used continuously for 3 months, some test subjects were concerned about whitening and cracking of their nails, which made them unsatisfactory.
比較例3は、皮膜形成主剤としてニトロセルロースを配
合していない為に、3ケ月間連続して使用しても爪に影
響を与えないものの、耐水性とメイクアップ効果の持続
性において満足し得るものでなかった。Comparative Example 3 does not contain nitrocellulose as the main film-forming agent, so it does not affect the nails even if used continuously for 3 months, but it is satisfactory in terms of water resistance and sustainability of the makeup effect. It was nothing.
比較例4は、炭素数2〜4の低級アルコールからなる揮
発性溶剤中にエタノールを80%以上含有していない為
に、光沢、硬度、屈曲性、耐水性。Comparative Example 4 has gloss, hardness, flexibility, and water resistance because it does not contain 80% or more of ethanol in a volatile solvent consisting of a lower alcohol having 2 to 4 carbon atoms.
メイクアップ効果の持続性において満足し得るものでな
かった。The durability of the makeup effect was not satisfactory.
(発明の効果)
以上記載のとと(、本発明は、光沢、硬度、屈曲性、耐
水性、メイクアップ効果の持続性において優れており、
かつ酢酸エチル、酢酸ブチル、トルエン等の溶剤を使用
することなく安全性にも優れた有用なる美爪料を提供す
ることは明らかである。(Effects of the Invention) As described above, the present invention is excellent in gloss, hardness, flexibility, water resistance, and durability of makeup effect,
Moreover, it is clear that a useful nail beauty preparation with excellent safety can be provided without using a solvent such as ethyl acetate, butyl acetate, or toluene.
Claims (1)
ルとを主要構成成分とする美爪料に於いて、低級アルコ
ール中のエタノール含有量が80重量%以上であること
を特徴とする美爪料。A nail beauty product containing L-type nitrocellulose and a lower alcohol having 2 to 4 carbon atoms as main components, characterized in that the ethanol content in the lower alcohol is 80% by weight or more. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23122788A JPH0278606A (en) | 1988-09-14 | 1988-09-14 | Manicure |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23122788A JPH0278606A (en) | 1988-09-14 | 1988-09-14 | Manicure |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0278606A true JPH0278606A (en) | 1990-03-19 |
Family
ID=16920314
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP23122788A Pending JPH0278606A (en) | 1988-09-14 | 1988-09-14 | Manicure |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0278606A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006016346A (en) * | 2004-07-02 | 2006-01-19 | Npr:Kk | Nail art solution |
JP2008303238A (en) * | 2007-06-05 | 2008-12-18 | Sumitomo Osaka Cement Co Ltd | Nitrocellulose solution and method for producing the same, phosphor slurry and method for producing the same, phosphor film, and fluorescent lamp |
JP2009221173A (en) * | 2008-03-18 | 2009-10-01 | Naris Cosmetics Co Ltd | Keratin status ameliorator |
-
1988
- 1988-09-14 JP JP23122788A patent/JPH0278606A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006016346A (en) * | 2004-07-02 | 2006-01-19 | Npr:Kk | Nail art solution |
JP2008303238A (en) * | 2007-06-05 | 2008-12-18 | Sumitomo Osaka Cement Co Ltd | Nitrocellulose solution and method for producing the same, phosphor slurry and method for producing the same, phosphor film, and fluorescent lamp |
JP2009221173A (en) * | 2008-03-18 | 2009-10-01 | Naris Cosmetics Co Ltd | Keratin status ameliorator |
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