JPS6033363B2 - nail polish remover - Google Patents
nail polish removerInfo
- Publication number
- JPS6033363B2 JPS6033363B2 JP3893378A JP3893378A JPS6033363B2 JP S6033363 B2 JPS6033363 B2 JP S6033363B2 JP 3893378 A JP3893378 A JP 3893378A JP 3893378 A JP3893378 A JP 3893378A JP S6033363 B2 JPS6033363 B2 JP S6033363B2
- Authority
- JP
- Japan
- Prior art keywords
- nail polish
- polish remover
- methyl
- dioxolane
- oxo
- 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
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 9
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 239000003205 fragrance Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 238000005429 filling process Methods 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
Landscapes
- Cosmetics (AREA)
Description
【発明の詳細な説明】
本発明は、爪上に塗布されたマニキュアを除去するため
のマニキュア除光液に関し、その目的とするところは、
安全で毒性の少ないマニキュア除光液を提供せんとする
にある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a nail polish remover for removing nail polish applied on nails, and its purpose is to:
Our goal is to provide a safe and less toxic nail polish remover.
従来、マニキュア除光液としてはアセトン、メチルエチ
ルケトン等の溶剤を主成分としたものが使用されている
。Conventionally, nail polish removers that contain solvents such as acetone and methyl ethyl ketone as main components have been used.
しかし、これらの溶剤は極めて引火性及び毒性が強く、
その製造、充填仕上げの工程において爆発、吸入による
毒性の危険に晒されるため防爆設備、換気装置等の十分
な設備を必要とすると共に、使用時においても刺激臭が
強く不快感を惹起し、溶解性が強すぎかつ蒸発速度が早
すぎるため爪が脱脂され、爪が白変する現象が生じると
か、皮膚に付着した場合皮膚の脱脂もひどく肌あれを起
す欠点があった。そのため、これにラノリン誘導体、イ
ソプロピルミリステート、ブチルステアレート、水等を
含有せしめて上記欠点を改善せんとする試みがなされて
いるが、未だ満足な結果は得られていない。斯る情況に
おいて、本発明者は上記欠点を解決せんと鋭意研究を行
った結果、２−オキソ−４−メチル−１・３−ジオキソ
ランと脂肪族アルコールとを主成分として含有する除光
液が上記欠点のない優れたものであることを見出し、本
発明を完成した。However, these solvents are extremely flammable and toxic.
During the manufacturing, filling and finishing process, they are exposed to the risk of explosion and toxicity due to inhalation, so they require sufficient equipment such as explosion-proof equipment and ventilation equipment, and even when used, they emit a strong pungent odor that causes discomfort, and melts. Because it is too strong and the evaporation rate is too fast, it degreases the nails, causing the nails to turn white, and when it comes in contact with the skin, it degreases the skin and causes severe roughness. Therefore, attempts have been made to improve the above drawbacks by incorporating lanolin derivatives, isopropyl myristate, butyl stearate, water, etc., but satisfactory results have not yet been obtained. Under such circumstances, the inventors of the present invention conducted intensive research to solve the above-mentioned drawbacks, and as a result, a nail polish remover containing 2-oxo-4-methyl-1,3-dioxolane and aliphatic alcohol as main components was developed. The present invention was completed based on the discovery that it is an excellent product that does not have the above-mentioned drawbacks.
本発明除光液の成分である２−オキソー４ーメチル−１
・３−ジオキソランは現在染着性を増大させるために梁
毛剤に、またウェーブ効果を発現させるために毛髪処理
剤に配合して使用されうろことが知られている極めて毒
性の少ない溶剤である。2-oxo-4-methyl-1, a component of the nail polish remover of the present invention
- 3-dioxolane is an extremely low-toxic solvent that is currently used in hair treatment agents to increase dyeability and in hair treatment agents to create a waving effect.
しかし、２−オキソ−４−メチル一１・３−ジオキソラ
ンの単独をマニキュア除光液として使用しても、爪上の
マニキュア塗布膜への浸透が遅く、その結果溶解性も悪
く、マニキュア除光液としての十分な機能は奏せられな
い。However, even when 2-oxo-4-methyl-1,3-dioxolane is used alone as a nail polish remover, it penetrates slowly into the nail polish coating film on the nails, resulting in poor solubility. It cannot function adequately as a liquid.
しかし、これに脂肪族アルコールを配合すると、マニキ
ュア塗膜への浸透性が早くなり、当該塗腰の熔解性が増
大し、有利に爪上のマニキュアを除光することができる
。脂肪族アルコールとしては、エタノール、ｎーブロパ
ノール、ｉ−プロパノールが好ましい。However, when an aliphatic alcohol is blended with this, the permeability into the nail polish coating becomes faster, the solubility of the coating increases, and the nail polish on the nails can be advantageously removed. As the aliphatic alcohol, ethanol, n-propanol, and i-propanol are preferred.
２−オキソ−４ーメチルー１・３−ジオキソランと脂肪
族アルコールとの配合割合は、マニキュア塗膜への浸透
性、塗膜の溶解性、乾燥性（除光後の乾燥速度）等の条
件を考慮し、重量比で１対１〜１球寸１、特に１．５対
１〜３対１が好ましい。The blending ratio of 2-oxo-4-methyl-1,3-dioxolane and aliphatic alcohol takes into account conditions such as permeability into the nail polish coating, solubility of the coating, and drying properties (drying speed after removal of light). However, the weight ratio is preferably 1:1 to 1 sphere size 1, particularly 1.5:1 to 3:1.
本発明のマニキュア除光液は、２ーオキソー４ーメチル
ー１・３−ジオキソランと脂肪族アルコールを均一に混
合すれば製造されるが、爪のトリートメント効果を得る
ために他の成分（例えば油分等）を配合することもでき
る。本発明マニキュア除光液の主成分である２ーオキソ
−４ーメチルー１・３ージオキソランの引火点（密閉式
）は約１３〆０であって、アセトンの−９００、メチル
エチルケトンの２００に比較し極めて高いため引火性は
低く、製造、充填仕上げ、保管等において安全であり、
また本除光液は刺激臭、不快臭がないと共に爪および皮
膚を脱脂して爪を白変させるとか肌あれを起す危険がな
い優れたものである。The nail polish remover of the present invention is produced by uniformly mixing 2-oxo-4-methyl-1,3-dioxolane and aliphatic alcohol, but other ingredients (such as oil) may be added in order to obtain a nail treatment effect. It can also be blended. The flash point (closed type) of 2-oxo-4-methyl-1,3-dioxolane, which is the main component of the nail polish remover of the present invention, is approximately 130, which is extremely high compared to -900 for acetone and 200 for methyl ethyl ketone. It has low flammability and is safe in manufacturing, filling and finishing, storage, etc.
Furthermore, this nail polish remover is excellent because it has no irritating or unpleasant odor, and there is no risk of degreasing the nails and skin, causing whitening of the nails or rough skin.
次に実施例を挙げて説明する。Next, an example will be given and explained.
尚、実施例中の配合量は重量部で示した。実施例 １
■ ２ーオキソ−４ーメチルー１・３ージオキソラン
７０．０
■ エタノール ３０．０
■ 色 素 適量■ 香
料 ０．１製法：■〜
■を均一に混合して製品する。In addition, the blending amounts in the examples are shown in parts by weight. Example 1 ■ 2-oxo-4-methyl-1,3-dioxolane
70.0
■ Ethanol 30.0
■ Appropriate amount of color ■ Fragrance
Fee 0.1 Manufacturing method: ■～
■ Mix evenly and make a product.
実施例 ２
■ ２ーオキソ−４ーメチルー１・３ージオキソラン
７５．０■
インブロピルアルコール ２５．０■
色 素 適量■ 香 料
０．１製法：実施例１
と同様にして製造する。Example 2 ■ 2-oxo-4-methyl-1,3-dioxolane
75.0■
Inbropyl alcohol 25.0■
Coloring agent Appropriate amount ■ Fragrance
0.1 Manufacturing method: Example 1
Manufactured in the same manner as.
実施例 ３
■ ２−オキソ−４−メチル−１・３−ジオキソラン
５５．０■
エタノール ４５．０■
コラーゲン誘導ポリベプタィド ０．３■ 色
素 適量■ 香 料
０．１製法：実施例１と同様
にして製造する。Example 3 ■ 2-oxo-4-methyl-1,3-dioxolane
55.0■
Ethanol 45.0■
Collagen-induced polypeptide 0.3■ Color
Basic appropriate amount■ Fragrance
0.1 Production method: Produced in the same manner as in Example 1.
実施例 ４
実施例１、２、３で得られた本発明品と従来品との物性
および使用上の効果を比較すれば次のとおりである。Example 4 The physical properties and usability effects of the products of the present invention obtained in Examples 1, 2, and 3 and the conventional products are compared as follows.
Claims (1)
脂肪族アルコールとを主成分として含有するマニキユア
除光液。1. A nail polish remover containing 2-oxo-4-methyl-1,3-dioxolane and an aliphatic alcohol as main components.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3893378A JPS6033363B2 (en) | 1978-04-03 | 1978-04-03 | nail polish remover |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3893378A JPS6033363B2 (en) | 1978-04-03 | 1978-04-03 | nail polish remover |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54132244A JPS54132244A (en) | 1979-10-15 |
| JPS6033363B2 true JPS6033363B2 (en) | 1985-08-02 |
Family
ID=12539020
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3893378A Expired JPS6033363B2 (en) | 1978-04-03 | 1978-04-03 | nail polish remover |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6033363B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6222709A (en) * | 1985-07-24 | 1987-01-30 | Suhama Kagaku Kk | Nail lacquer remover |
| JP5241300B2 (en) * | 2008-04-17 | 2013-07-17 | 三菱鉛筆株式会社 | Solid nail remover |
-
1978
- 1978-04-03 JP JP3893378A patent/JPS6033363B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS54132244A (en) | 1979-10-15 |
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