JPS6033364B2 - Improved enamel remover composition - Google Patents
Improved enamel remover compositionInfo
- Publication number
- JPS6033364B2 JPS6033364B2 JP4101278A JP4101278A JPS6033364B2 JP S6033364 B2 JPS6033364 B2 JP S6033364B2 JP 4101278 A JP4101278 A JP 4101278A JP 4101278 A JP4101278 A JP 4101278A JP S6033364 B2 JPS6033364 B2 JP S6033364B2
- Authority
- JP
- Japan
- Prior art keywords
- alcohol
- water
- composition
- weight
- phenoxyalkanol
- 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
- 210000003298 dental enamel Anatomy 0.000 title claims description 24
- 239000000203 mixture Substances 0.000 title claims description 23
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 26
- 235000019441 ethanol Nutrition 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
- 125000001931 aliphatic group Chemical group 0.000 claims description 11
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 claims description 7
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 4
- -1 3-phenoxypropyl alcohol Chemical compound 0.000 claims description 3
- LOJHHQNEBFCTQK-UHFFFAOYSA-N 2-phenoxypropan-1-ol Chemical compound OCC(C)OC1=CC=CC=C1 LOJHHQNEBFCTQK-UHFFFAOYSA-N 0.000 claims description 2
- OYQUCYCSSADEIC-UHFFFAOYSA-N 4-phenoxybutan-1-ol Chemical compound OCCCCOC1=CC=CC=C1 OYQUCYCSSADEIC-UHFFFAOYSA-N 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 229940035429 isobutyl alcohol Drugs 0.000 claims description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 3
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 230000000052 comparative effect Effects 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 230000001954 sterilising effect Effects 0.000 description 8
- 230000002087 whitening effect Effects 0.000 description 7
- 230000000249 desinfective effect Effects 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 5
- 239000002932 luster Substances 0.000 description 4
- 238000004659 sterilization and disinfection Methods 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000001747 exhibiting effect Effects 0.000 description 3
- 239000006096 absorbing agent Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 230000003203 everyday effect Effects 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- ZUAURMBNZUCEAF-UHFFFAOYSA-N 2-(2-phenoxyethoxy)ethanol Chemical compound OCCOCCOC1=CC=CC=C1 ZUAURMBNZUCEAF-UHFFFAOYSA-N 0.000 description 1
- 241000219112 Cucumis Species 0.000 description 1
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
- 206010013911 Dysgeusia Diseases 0.000 description 1
- 229920000715 Mucilage Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- MHYCRLGKOZWVEF-UHFFFAOYSA-N ethyl acetate;hydrate Chemical compound O.CCOC(C)=O MHYCRLGKOZWVEF-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Landscapes
- Cosmetics (AREA)
Description
【発明の詳細な説明】
本発明は、改良されたエナメルリムーバ−組成物に関し
、詳しくは、使用時に爪をいためたり、白化する弊害な
く、消毒殺菌効果を発揮しながらネイルエナメルを溶解
除去すると共に、爪に良好なガラス様光沢を付与し得る
不燃性のエナメルリムーバー組成物に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improved enamel remover composition, and more specifically, it dissolves and removes nail enamel while exhibiting a disinfecting and sterilizing effect without damaging or bleaching nails during use. , relates to a non-flammable enamel remover composition capable of imparting a good glass-like gloss to nails.
従来、エナメルリムーバー(ネイルエナメルリムーバー
)としては、アルコール、低級アルコールのェステル等
の有機溶剤系のものや、それらの水涙天01性有機溶剤
と水との組合せからなるもの(水温和性有機溶剤−水系
)がよく知られている。Conventionally, enamel removers (nail enamel removers) include those based on organic solvents such as alcohol and lower alcohol esters, and those made of a combination of these hydrophilic organic solvents and water (water-miscible organic solvents). -water-based) is well known.
しかしながら、有機溶剤系のりムーバーは、衣類の色素
を溶解したり、直接爪の水分が脂肪を過度に溶解して爪
の表面をいためたり、爪を白化する等の他に、引火、燃
焼、爆発等の危険性を有する等の致命的な欠陥がある。However, organic solvent-based glue movers can cause ignition, combustion, explosion, etc., as well as dissolving the pigments in clothing, damaging the surface of the nails by directly dissolving the moisture in the nails excessively and damaging the nail surfaces, and causing the nails to become white. There are fatal flaws such as posing risks such as
一方、前記の水混和性有機溶剤−水系のリムーバーでは
、引火、爆発等の危険性が少ない反面、火婿を接近する
と燃焼し易いか、直接接触すると燃焼するものが多く、
また爪をいためたり、白化しやすい等の欠点も充分改良
されていない。本発明者等は、従来技術の欠点を改良せ
んとして鋭意研究した結果、後記一般式で表わされるフ
ェノキシアルカノールと脂肪族低級アルコールと水が適
量濃熔した組成物は、前記エナメルリムーバーの欠点が
悉く改良されたおり、しかも使用時に消毒殺菌効果をも
発現し得ることを見出し本発明を完成した。本発明の目
的は、使用時に爪をいためたり、白化する等の弊害なく
、消毒、殺菌効果を発揮しながらネイルエナメルを溶解
除去し、爪に良好なガラス様光沢を付与し得る不燃性の
新規なエナメルリムーバ−組成物を提供することもある
。On the other hand, while the above-mentioned water-miscible organic solvent-water-based removers have little risk of ignition or explosion, many of them tend to combust when brought close to a flame or when brought into direct contact.
Further, drawbacks such as damage to nails and easy whitening have not been sufficiently improved. As a result of intensive research aimed at improving the shortcomings of the prior art, the present inventors have discovered that a composition in which phenoxyalkanol represented by the general formula shown below, an aliphatic lower alcohol, and water are melted together in appropriate amounts overcomes all the shortcomings of the above-mentioned enamel remover. The present invention was completed by discovering that an improved cage can also exhibit a disinfecting and sterilizing effect during use. The object of the present invention is to provide a novel, non-flammable product that can dissolve and remove nail enamel while exhibiting disinfecting and sterilizing effects without damaging nails or causing whitening during use, and that can impart a good glass-like luster to nails. Enamel remover compositions may also be provided.
すなわち、本発明は、 一般式 (Rは炭素数2〜4のアルキルン基である。That is, the present invention general formula (R is an alkyl group having 2 to 4 carbon atoms.
)で表わされるフェノキシアルカノールと脂肪族低級ア
ルコールと水が涙溶していることを特徴とする改良され
たエナメルリムーバ−組成物である。本発明に使用する
前記一般式で示されるフェノキシアルカノールとしては
、例えば、2−フェノキシエチルアルコール、3ーフエ
ノキシプロピルアルコール、2−フエノキシプロピルア
ルコール、4−フェノキシブチルアルコール等を挙げる
ことができる。それらの中で2ーフェノキシエチルアル
コールが最も好ましい。該フヱノキシアルカノールは、
1つ、又は二つ以上組合せて使用される。上記のフェノ
キシアルカノールは水に難溶、アルコールに易溶の軽快
なる芳香を有する粘穂の液体であって、人体に対する刺
激や毒性が無い上に、高度の消毒、殺菌性を有してる。
フェノキシアルカノールの使用量(含有量)は、組成物
全量に対して30〜65重量%好ましくは35〜6の重
量%である。This is an improved enamel remover composition characterized in that the phenoxyalkanol represented by (), the aliphatic lower alcohol, and water are dissolved in water. Examples of the phenoxyalkanol represented by the above general formula used in the present invention include 2-phenoxyethyl alcohol, 3-phenoxypropyl alcohol, 2-phenoxypropyl alcohol, and 4-phenoxybutyl alcohol. can. Among them, 2-phenoxyethyl alcohol is most preferred. The phenoxyalkanol is
One or more may be used in combination. The above-mentioned phenoxyalkanol is a mucilage liquid with a light aroma that is sparingly soluble in water and easily soluble in alcohol, and is non-irritating or toxic to the human body, and has high disinfecting and sterilizing properties.
The amount (content) of the phenoxyalkanol used is 30 to 65% by weight, preferably 35 to 6% by weight, based on the total amount of the composition.
3の重量%よりも少ないと使用時の爪に対するガラス様
光沢の付与効果及び消毒、殺菌効果の低下や爪の白化を
きたしやすく、65重量%よりも多くなると不燃性の低
下(燃え易くなる)や感触の劣化をきたしやすい。If it is less than 3% by weight, the effect of imparting a glass-like luster to nails during use, as well as the disinfection and sterilization effects, will likely decrease, and the nails will become white, and if it exceeds 65% by weight, the non-flammability will decrease (easily flammable). It is easy to cause deterioration in texture and feel.
フェノキシアルカノールは前記の如く水に雛熔で親水性
が低いけれども、脂肪族低級アルコールの共存によって
、比較的多量のフェノキシアルカノールを安定に混落し
て均一系を保持し得る。本発明に使用される脂肪族低級
アルコールとしては、例えばエチルアルコール、n−プ
チルアルコール、イソブチルアルコール等が挙げられる
。Although phenoxyalkanol dissolves in water and has low hydrophilicity as described above, the coexistence of an aliphatic lower alcohol allows a relatively large amount of phenoxyalkanol to be stably mixed in to maintain a homogeneous system. Examples of the aliphatic lower alcohol used in the present invention include ethyl alcohol, n-butyl alcohol, and isobutyl alcohol.
脂肪族低級アルコールは、一つ又は二つ以上組合せて使
用され、その使用量(含有量)は、組成物全量に対して
15〜4の重量%、好ましくは20〜35重量%である
。15重量%よりも少なくなるとネイルエナメルの熔解
性(落ち)や感触がわろくなり、また不均一系を形成し
やすく、4の重量%よりも多くなると燃えやすく、使用
時に爪が白化しやすくなる。One or more aliphatic lower alcohols are used in combination, and the amount (content) used is 15 to 4% by weight, preferably 20 to 35% by weight, based on the total amount of the composition. If it is less than 15% by weight, the solubility (falling) and feel of the nail enamel will be poor, and it will tend to form a non-uniform system, and if it is more than 4% by weight, it will be more likely to burn and the nails will be more likely to whiten during use. .
水の使用量は、組成物全量に対して10〜40重量%、
好ましくは15〜35重量%である。10重量%よりも
少なくなると燃えやすくなり、4の重量%よりも多くな
るとネイルエナメルの溶解性が低下し、また組成物が不
均一系を形成しやすい。The amount of water used is 10 to 40% by weight based on the total amount of the composition,
Preferably it is 15 to 35% by weight. If it is less than 10% by weight, it becomes easily flammable, and if it is more than 4% by weight, the solubility of the nail enamel decreases, and the composition tends to form a heterogeneous system.
本発明のエナメルリムーバー組成物には、必要に応じて
、香料、染料等の着色剤、紫外線吸収剤等を添加使用す
ることができる。本発明のエナメルリムーバー組成物は
、前記のフェノキシアルカノール、脂肪族低級アルコー
ルと水、又は必要に応じて香料、着色剤、紫外線吸収剤
等の慣用添加物を雌梓下に適宜順序で添加、混合するこ
とによって製造される。The enamel remover composition of the present invention may contain fragrances, colorants such as dyes, ultraviolet absorbers, and the like, if necessary. The enamel remover composition of the present invention is prepared by adding and mixing the above-mentioned phenoxyalkanol, aliphatic lower alcohol and water, or, if necessary, conventional additives such as fragrances, colorants, and ultraviolet absorbers in an appropriate order. Manufactured by
本発明のエナメルリムーバー組成物は、前記構成の三成
分が混溶した新規な組成物であって、実質的に透明、均
一な不燃性の液体で、かつ、脱脂力も適度であるため使
用時に爪をいためたり白化する等の弊害がなく、そして
消毒殺菌効果を発揮してながらネイルエナメルを溶解除
去すると同時にガラス様の良好な光沢を付与することが
できる。The enamel remover composition of the present invention is a novel composition in which the three components described above are mixed together, and it is a substantially transparent, uniform, nonflammable liquid, and has an appropriate degreasing power, so it can be used to remove nails. It does not cause harmful effects such as damaging nails or whitening, and while exhibiting a disinfecting and sterilizing effect, it can dissolve and remove nail enamel and at the same time give a good glass-like gloss.
就中、脂肪族低級アルコールは、水混和性の低い前記フ
ェノキシァルカノールを安定に混和し、かつフェノキシ
アルカノールの適量混和によって、有機溶媒系や脂肪族
低級アルコール水系のリムーバ−の前記欠点を悉く改良
し、同時に前記リムーバーに見られない消毒殺菌効果や
良好なガラス様光沢を瓜に付与し得る本発明の作用効果
の特異性は著しい。In particular, aliphatic lower alcohols can be stably mixed with the phenoxyalkanol, which has low water miscibility, and by mixing an appropriate amount of phenoxyalkanol, all the above-mentioned drawbacks of organic solvent-based and aliphatic lower alcohol water-based removers can be improved. However, at the same time, the specificity of the effects of the present invention is remarkable, as it can impart a disinfecting and sterilizing effect and a good glass-like luster to melons, which are not seen in the above-mentioned removers.
以下、本発明の実施例について詳説する。実施例に示す
部とは重量部を、%とは重量%を意味する。Examples of the present invention will be described in detail below. In the examples, parts mean parts by weight, and % means weight %.
エナメルリムーバー試料の性能試験は、特定のネイルエ
ナメルを使用して行ない、女性20人をパネラーとして
毎日3週間行なった結果及び専門技術者3人が毎日3週
間行なった結果を示した。エナメルリムーバーの燃焼性
は、リムーバーを時計皿に入れた後、ライターの火焔(
火稲長一定)をリムーバーに直接接触して、燃えたもの
は燃焼燃えなかったものは不燃とした。実施例 1
2−フェノキシェチルアルコール48部、エチルアルコ
ール31部と水21部を混合機に容れ、3粉ご間礎梓混
合して、透明均一な本発明のエナメルリムーバーを得た
。The performance test of the enamel remover sample was conducted using a specific nail enamel, and the results are shown in which 20 female panelists conducted the test every day for 3 weeks, and 3 professional technicians conducted the test every day for 3 weeks. The flammability of enamel remover is determined by the flame of a lighter (
Those that burned were placed in direct contact with the remover, and those that did not burn were considered non-flammable. Example 1 48 parts of 2-phenoxyethyl alcohol, 31 parts of ethyl alcohol, and 21 parts of water were placed in a mixer, and the three powders were mixed to obtain a transparent and uniform enamel remover of the present invention.
次に前記と同様に蝿拝混合して、エチルアルコール7賭
Bと水21部とからなる比較例1のリムーバー及びエチ
ルアルコール21部と水7$部からなる比較例2のリム
ーバーを得た。Next, they were mixed in the same manner as described above to obtain a remover of Comparative Example 1 consisting of 7 parts of ethyl alcohol and 21 parts of water, and a remover of Comparative Example 2 consisting of 21 parts of ethyl alcohol and 7 parts of water.
更に2−フヱノキシェチルアルコールの代りに類縁化合
物としてジヱチレングリコールモノフェニルェーテルを
使用する他は、前記本発明と同機にして比較例3のリム
ーバーを得た。Furthermore, a remover of Comparative Example 3 was obtained using the same machine as the present invention except that diethylene glycol monophenyl ether was used as a related compound instead of 2-phenoxyethyl alcohol.
上記の本発明のリムーバー及び比較例1〜3の各リムー
バーについての実用テストを女性20人のパネラーによ
って行なった結果を第1表に示した。Table 1 shows the results of a practical test conducted by a panel of 20 women on the remover of the present invention and the removers of Comparative Examples 1 to 3.
尚、専門技術者が行なったりムーバ−の燃焼性テストの
結果を第1表に併記した。第 1 表
試 験 項 目 本発明品 比較例1 比
較例2 比較例3消毒・殺菌効果
有 殆んど簾 無 舞燃 焼
性 不燃 燃焼 不燃
不燃使用後の感触が良い
13へ 10へ 11人 10人
〃 が普通 5
4 6 8〃 が悪、い
2 6
3 2除去効果が良い
11 4 0
1〃 が普通
9 14 0 1
0〃 が悪い 0
2 20 9爪の表面が異伏に
白くなる 0 18
6 1〃 に異伏を認めをい
20 2 14 19
良好なガラス様光沢が付いた 15
0 0 1ガラス様ではを
いが光沢が付いた 4 0
0 1光沢が付かなかった
1 20 20
18以上の如く、本発明のリムーバーは、比較例の
リムーバ−使用時における爪の白化(異状に白くなる)
燃焼する等の欠点を改良しており、比較例のリムーバー
には見られない良好なガラス様光沢を爪に付与すること
ができ、またネイルエナメルの除去効果も比較的良好で
ある。Table 1 also shows the results of the flammability test of the mover, which was conducted by a professional engineer. Table 1 Test Item Inventive product Comparative example 1 Comparative example 2 Comparative example 3 Disinfection/sterilization effect
Yes Mostly blinds No mai-yaki
Characteristic Non-flammable Combustible Non-combustible Non-combustible Feels good after use
Go to 13 Go to 10 11 people 10 people is normal 5
4 6 8 is bad.
2 6
3 Good removal effect
11 4 0
1 is normal
9 14 0 1
0〃 Bad 0
2 20 9 The surface of the nail becomes strangely white 0 18
6 1. Please acknowledge the abjection.
20 2 14 19
With good glass-like luster 15
0 0 1 Glass-like and shiny 4 0
0 1 Not shiny
1 20 20
As described above, the remover of the present invention does not cause whitening of nails (unnatural whitening) when using the remover of the comparative example.
It has improved drawbacks such as burning, can give nails a good glass-like gloss that is not seen in the remover of the comparative example, and has a relatively good nail enamel removal effect.
実施例 2
2−フェノキシェチルアルコールを48部、エチルアル
コールの代りにインプロピルアルコールを3碇都、水を
2群部使用する他は実施例1の本発明と同様にして均一
透明な本発明のリムーバーを製造した。Example 2 A uniformly transparent invention was prepared in the same manner as in Example 1 except that 48 parts of 2-phenoxyethyl alcohol, 3 parts of inpropyl alcohol instead of ethyl alcohol, and 2 parts of water were used. Manufactured a remover.
このリムーバーについて、専門技術者3人が実施した実
用テストの結果は、不燃性で、使用時に爪をいためたり
、白化することがなく、市販品に見られない良好なガラ
ス様光沢が付与されること、ネイルエナメルの除去効果
は比較的良好であることを認めている。The results of a practical test conducted by three expert engineers on this remover showed that it is non-flammable, does not damage or whiten nails when used, and provides a good glass-like gloss not found in commercially available products. It is acknowledged that the nail enamel removal effect is relatively good.
実施例 3
3ーフェノキシプロピルアルコール45部、n−プロピ
ルアルコール28部、水27部を使用し実施例1と同様
に濃伴下に混合して均一透明な本発明のリムーバーを製
造した。Example 3 45 parts of 3-phenoxypropyl alcohol, 28 parts of n-propyl alcohol, and 27 parts of water were mixed together in the same manner as in Example 1 to produce a uniformly transparent remover of the present invention.
このリムーバ−について、専門技術者3人が実施した実
用テストの結果は不燃性で、使用時に爪をいためたり、
白化することがなく、市販品に見られない良好なガラス
様光沢が付与されること、ネイルエナメルの除去効果は
比較的良好であることを認めている。The results of a practical test conducted by three professional engineers on this remover revealed that it is non-flammable and will not damage your nails when used.
It has been recognized that it does not cause whitening, provides a good glass-like gloss not found in commercially available products, and has a relatively good nail enamel removal effect.
実施例 4
構成成分の組成を、下記の第2表の通りする他は、実施
例1と同様にして本発明(No.1〜No.8)及び比
較例(No.9〜13)のIJムーバーを製造した。Example 4 IJs of the present invention (No. 1 to No. 8) and comparative examples (No. 9 to 13) were prepared in the same manner as in Example 1, except that the composition of the constituent components was as shown in Table 2 below. Manufactured a mover.
その性能を第2表に示した。第 2 表
試料修 PEA EA 水 燃焼性 後感触 除去効
果 爪の白化 光 沢1 30 32
38 不燃 略良好 略良好 無 良好なガ
ラス様光沢2 65 2015 〃 〃 〃
〃 〃3 63 1522 〃 〃 〃
〃 〃4 37 40 23 〃 〃
〃 〃 〃5 60 3010 〃
〃 〃 〃 〃6 32 28 4
0 〃 ″ 〃 〃 〃7
48 31 21 ″ 〃 ″
″ 極めて良好なガラ力廉光沢8 38
37 25 〃 〃 〃 〃 〃
9 25 36 39 〃 〃 〃 ややあ
り 無10 70 20 10 燃焼 不
良 〃 無 良好なガラス様光沢11
60 10 30 不均一系(二層分離)を形成1
2 38 45 17 燃焼 やや不良 普
通 有 無13 54 40
6 〃 普通 良好 無 良好を
ガラス様光沢14 38 17 45 不均一
系(二層分離)を形成注:PEAは2−フェノキシェチ
ルアルコール、EAはエチルアルコールである。Its performance is shown in Table 2. Table 2 Sample repair PEA EA Water Flammability Aftertaste Removal effect Nail whitening Gloss 1 30 32
38 Nonflammability Approximately good Approximately good None Good glass-like gloss 2 65 2015 〃 〃 〃
〃 〃3 63 1522 〃 〃 〃
〃 〃4 37 40 23 〃 〃
〃 〃 〃5 60 3010 〃
〃 〃 〃 〃6 32 28 4
0 〃 ″ 〃 〃 〃7
48 31 21 ″ 〃 ″
″ Extremely good glass strength and gloss 8 38
37 25 〃 〃 〃 〃 〃
9 25 36 39 〃 〃 〃 Slightly absent 10 70 20 10 Poor combustion 〃 None Good glass-like gloss 11
60 10 30 Forming a heterogeneous system (two-layer separation) 1
2 38 45 17 Combustion Slightly poor Normal Yes No 13 54 40
6 〃 Fair Good None Good: Glass-like gloss 14 38 17 45 Formation of a heterogeneous system (two-layer separation) Note: PEA is 2-phenoxyethyl alcohol, and EA is ethyl alcohol.
Claims (1)
ルコールと水が混溶していることを特徴とする改良され
たエナメルリムーバー組成物。2 フエノキシアルカノ
ールが、2−フエノキシエチルアルコール、3−フエノ
キシプロピルアルコール、2−フエノキシプロピルアル
コール、4−フエノキシブチルアルコールあるいはそれ
らの組合せである特許請求の範囲第1項記載の組成物。 3 フエノキシアルカノールが、30〜65重量%混溶
している特許請求の範囲1項記載の組成物。 4 脂肪族低級アルコールが、エチルアルコール、n−
プロピルアルコール、イソプロピルアルコール、n−ブ
チルアルコール、イソ−ブチルアルコールあるいはそれ
らの組合せである特許請求の範囲第1項記載の組成物。 5 脂肪族低級アルコールが、15〜40重量%混溶し
ている特許請求の範囲第1項記載の組成物。6 水が、
10〜40重量%混溶している特許請求の範囲第1項記
載の組成物。[Claims] 1 A phenoxyalkanol and an aliphatic lower alcohol represented by the general formula ▲ Numerical formula, chemical formula, table, etc. ▼ (In the formula, R is an alkylene group having 2 to 4 carbon atoms.) An improved enamel remover composition characterized by containing a mixture of and water. 2. Claim 1, wherein the phenoxyalkanol is 2-phenoxyethyl alcohol, 3-phenoxypropyl alcohol, 2-phenoxypropyl alcohol, 4-phenoxybutyl alcohol, or a combination thereof. Compositions as described in Section. 3. The composition according to claim 1, wherein the phenoxyalkanol is mixed in an amount of 30 to 65% by weight. 4 The aliphatic lower alcohol is ethyl alcohol, n-
The composition of claim 1 which is propyl alcohol, isopropyl alcohol, n-butyl alcohol, iso-butyl alcohol or a combination thereof. 5. The composition according to claim 1, wherein the aliphatic lower alcohol is mixed in an amount of 15 to 40% by weight. 6 Water is
The composition according to claim 1, wherein the composition is mixed in an amount of 10 to 40% by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4101278A JPS6033364B2 (en) | 1978-04-06 | 1978-04-06 | Improved enamel remover composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4101278A JPS6033364B2 (en) | 1978-04-06 | 1978-04-06 | Improved enamel remover composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54135235A JPS54135235A (en) | 1979-10-20 |
| JPS6033364B2 true JPS6033364B2 (en) | 1985-08-02 |
Family
ID=12596472
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4101278A Expired JPS6033364B2 (en) | 1978-04-06 | 1978-04-06 | Improved enamel remover composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6033364B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12207667B2 (en) | 2008-07-09 | 2025-01-28 | Starbucks Corporation | Soluble coffee products for producing beverages with enhanced flavors and aromas |
-
1978
- 1978-04-06 JP JP4101278A patent/JPS6033364B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12207667B2 (en) | 2008-07-09 | 2025-01-28 | Starbucks Corporation | Soluble coffee products for producing beverages with enhanced flavors and aromas |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS54135235A (en) | 1979-10-20 |
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