JPWO2009075142A1 - Bactericidal detergent composition - Google Patents
Bactericidal detergent composition Download PDFInfo
- Publication number
- JPWO2009075142A1 JPWO2009075142A1 JP2009545367A JP2009545367A JPWO2009075142A1 JP WO2009075142 A1 JPWO2009075142 A1 JP WO2009075142A1 JP 2009545367 A JP2009545367 A JP 2009545367A JP 2009545367 A JP2009545367 A JP 2009545367A JP WO2009075142 A1 JPWO2009075142 A1 JP WO2009075142A1
- Authority
- JP
- Japan
- Prior art keywords
- polyoxyethylene
- foam
- detergent composition
- mass
- ether
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 61
- 239000003599 detergent Substances 0.000 title claims abstract description 51
- 230000000844 anti-bacterial effect Effects 0.000 title description 8
- -1 polyoxyethylene Polymers 0.000 claims abstract description 71
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims abstract description 62
- 239000006260 foam Substances 0.000 claims abstract description 52
- 230000001954 sterilising effect Effects 0.000 claims abstract description 48
- 239000004359 castor oil Substances 0.000 claims abstract description 29
- 235000019438 castor oil Nutrition 0.000 claims abstract description 29
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims abstract description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 15
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 13
- 150000001413 amino acids Chemical class 0.000 claims abstract description 11
- 150000003839 salts Chemical class 0.000 claims abstract description 11
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 claims abstract description 10
- 125000002091 cationic group Chemical group 0.000 claims abstract description 10
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- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 8
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- 229960001927 cetylpyridinium chloride Drugs 0.000 claims description 6
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 claims description 6
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- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 4
- LQXBZWFNAKZUNM-UHFFFAOYSA-N 16-methyl-1-(16-methylheptadecoxy)heptadecane Chemical compound CC(C)CCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCC(C)C LQXBZWFNAKZUNM-UHFFFAOYSA-N 0.000 description 4
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- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 3
- 239000003899 bactericide agent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
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- SPSPIUSUWPLVKD-UHFFFAOYSA-N 2,3-dibutyl-6-methylphenol Chemical compound CCCCC1=CC=C(C)C(O)=C1CCCC SPSPIUSUWPLVKD-UHFFFAOYSA-N 0.000 description 2
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- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
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- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
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- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
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- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
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Landscapes
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- Medicinal Preparation (AREA)
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- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
（Ａ）カチオン性殺菌剤、（Ｂ−１）ＨＬＢ９〜１６のポリオキシエチレン硬化ヒマシ油、モノステアリン酸ポリオキシエチレングリセリン及びモノステアリン酸ポリエチレングリコールから選ばれるノニオン性界面活性剤、（Ｃ）アミノ酸又はその塩、及び（Ｄ）炭素数１〜３のアルコール１６〜４０質量％を含有し、フォーマー容器に充填してなり泡状に吐出されることを特徴とする、洗い流さないタイプの殺菌清浄剤組成物。(A) Cationic fungicide, (B-1) Nonionic surfactant selected from polyoxyethylene hydrogenated castor oil of HLB 9-16, polysoxyethylene glyceryl monostearate and polyethylene glycol monostearate, (C) amino acid Or a salt thereof, and (D) a sterilizing detergent of non-washing type, characterized by containing 16 to 40% by mass of an alcohol having 1 to 3 carbon atoms, filled in a former container and discharged in the form of foam. Composition.
Description
本発明は、泡で使用する洗い流さないタイプの殺菌清浄剤組成物に関するものである。 The present invention relates to a non-washing type sterilizing detergent composition for use with foam.
従来の殺菌剤洗浄剤では洗い流すものが主流であり、外出先やリビング等水のないところでの使用は困難であり、その剤型はジェル状（特許文献１：特許第３４９９８８２号公報参照）やスプレー状であった。しかしながら、ジェル状の消毒剤は、添加している増粘剤により使用後のべたつきが残る等の使用感の上で問題があり、スプレー状のものは床等に飛び散る等の使用性に問題があった。一方、殺菌清浄剤を泡にする技術が提案されているが（特許文献２：特開平１０−３３０７９９号公報、特許文献３：特開２００１−１３９９９３号公報、特許文献４：特開昭６２−１３５４１０号公報参照）、乾きが遅く、手に広げた後も泡が残ったり、泡保形性が悪いという問題があった。以上のことから、手に取ったときは泡保形性があり手から垂れにくく、手に広げた後は、適度な時間で消泡し、泡残りがなく、かつ乾きやすい、泡で使用する洗い流さないタイプの殺菌清浄剤組成物が望まれていた。 In conventional disinfectant cleaning agents, the mainstream is washing away, and it is difficult to use in places where there is no water, such as on the go or in the living room. The dosage form is gel (see Patent Document 1: Japanese Patent No. 3499882) or spray. It was in the shape. However, gel-like disinfectants have problems in terms of usability such as stickiness after use due to the thickener added, and spray-like disinfectants have problems in usability such as splashing on the floor. there were. On the other hand, techniques for foaming a sterilizing detergent have been proposed (Patent Document 2: Japanese Patent Laid-Open No. 10-330799, Patent Document 3: Japanese Patent Laid-Open No. 2001-139993, Patent Document 4: Japanese Patent Laid-Open No. 62-62). No. 135410), drying was slow, and there was a problem that foam remained even after spreading on the hand, and foam shape retention was poor. From the above, when held in a hand, it has foam-retaining properties and is difficult to drip from the hand. A bactericidal detergent composition of the type that does not wash away has been desired.
本発明は上記事情に鑑みなされたもので、手に取ったときは泡保形性があり手から垂れにくく、手に広げた後は、適度な時間で消泡し、泡残りがなくかつ乾きやすい、洗い流さないタイプの殺菌清浄剤組成物を提供することを目的とする。 The present invention has been made in view of the above circumstances, and when held in the hand, has a foam-retaining property and is difficult to drip from the hand. An object of the present invention is to provide a sterilizing detergent composition which is easy and does not wash away.
本発明者らは、上記目的を達成するため鋭意検討した結果、カチオン性殺菌剤を含有する殺菌清浄剤組成物に、特定のノニオン性界面活性剤とアミノ酸又はその塩の組合せによって、炭素数１〜３のアルコールを配合しても、手に取ったときは泡保形性があり手から垂れにくいという性質を有する一方、手に広げた後は、適度な時間で消泡し、泡残りがなくかつ乾きやすい洗い流さないタイプの殺菌清浄剤組成物が得られることを知見し、本発明をなすに至ったものである。手に取ったときの泡の垂れにくさは、泡の保形性と相関があり、保形成性の良好なものほど手に取ったとき泡は垂れにくく、使用性上良好である。一方で、手に取った泡が適度な時間で消えて流動性のある液体となることにより、手指に擦り込みやすく、使用性上良好である。このように本発明の構成とすることにより格別な作用効果が発揮されることは、上記従来技術からは予想し難いものであり、本発明者が新たに見出したものである。 As a result of intensive studies to achieve the above object, the present inventors have determined that a sterilizing detergent composition containing a cationic sterilizing agent has a carbon number of 1 by combining a specific nonionic surfactant and an amino acid or a salt thereof. Even if it is blended with ~ 3 alcohol, it has the property of being foam-retaining and difficult to drip from the hand when taken in the hand. The present inventors have found that a sterilizing detergent composition that is easy to dry and does not wash away can be obtained, and has led to the present invention. The difficulty of dripping bubbles when picked up is correlated with the shape-retaining properties of the bubbles, and the better the shape-holding properties, the more difficult the bubbles drip when picked up by the hand, which is good in terms of usability. On the other hand, since the foam taken in the hand disappears in a proper time and becomes a fluid liquid, it is easy to rub into the fingers and is good in terms of usability. Thus, it is difficult to predict from the above prior art that a special effect is exhibited by the configuration of the present invention, and the present inventor has newly found out.
従って、本発明は下記殺菌清浄剤組成物を提供する。
［１］．（Ａ）カチオン性殺菌剤、（Ｂ−１）ＨＬＢ９〜１６のポリオキシエチレン硬化ヒマシ油、モノステアリン酸ポリオキシエチレングリセリン及びモノステアリン酸ポリエチレングリコールから選ばれるノニオン性界面活性剤、（Ｃ）アミノ酸又はその塩、及び（Ｄ）炭素数１〜３のアルコール１６〜４０質量％を含有し、フォーマー容器に充填してなり泡状に吐出されることを特徴とする、洗い流さないタイプの殺菌清浄剤組成物。
［２］．（Ａ）カチオン性殺菌剤、（Ｂ−２）ＨＬＢ１０〜１４の下記一般式（１）
で表されるポリオキシエチレン分岐アルキルエーテル及びポリオキシエチレンコレステリルエーテルから選ばれるノニオン性界面活性剤、（Ｃ）アミノ酸又はその塩、及び（Ｄ）炭素数１〜３のアルコール３０〜７０質量％を含有し、フォーマー容器に充填してなり泡状に吐出されることを特徴とする、洗い流さないタイプの殺菌清浄剤組成物。
［３］．（Ａ）成分が、塩化ベンザルコニウム、塩化ベンゼトニウム又は塩化セチルピリジニウムである［１］又は［２］記載の殺菌清浄剤組成物。Accordingly, the present invention provides the following bactericidal detergent composition.
[1]. (A) Cationic fungicide, (B-1) Nonionic surfactant selected from polyoxyethylene hydrogenated castor oil of HLB 9-16, polysoxyethylene glyceryl monostearate and polyethylene glycol monostearate, (C) amino acid Or a salt thereof, and (D) a sterilizing detergent of non-washing type, characterized by containing 16 to 40% by mass of an alcohol having 1 to 3 carbon atoms, filled in a former container and discharged in the form of foam. Composition.
[2]. (A) Cationic fungicide, (B-2) HLB 10-14, following general formula (1)
A nonionic surfactant selected from polyoxyethylene branched alkyl ether and polyoxyethylene cholesteryl ether represented by: (C) an amino acid or a salt thereof, and (D) 30 to 70% by mass of an alcohol having 1 to 3 carbon atoms. A sterilizing detergent composition of a non-washing type, characterized in that it is contained, filled in a former container and discharged in the form of foam.
[3]. The sterilizing detergent composition according to [1] or [2], wherein the component (A) is benzalkonium chloride, benzethonium chloride or cetylpyridinium chloride.
本発明によれば、手に取ったときは泡保形性があり手から垂れにくいという性質を有する一方、手に広げた後は、適度な時間で消泡し、泡残りがなくかつ乾きやすい泡で使用する洗い流さないタイプの殺菌清浄剤組成物を提供することができる。 According to the present invention, when held in the hand, the foam has a shape-retaining property and is difficult to drip from the hand. A non-washing type sterilizing detergent composition for use with foam can be provided.
以下、本発明について更に詳しく説明する。
本発明の第１の殺菌清浄剤組成物は、（Ａ）カチオン性殺菌剤、（Ｂ−１）ＨＬＢ９〜１６のポリオキシエチレン硬化ヒマシ油、モノステアリン酸ポリオキシエチレングリセリン及びモノステアリン酸ポリエチレングリコールから選ばれるノニオン性界面活性剤、（Ｃ）アミノ酸又はその塩、及び（Ｄ）炭素数１〜３のアルコール１６〜４０質量％を含有し、フォーマー容器に充填してなり泡状に吐出されることを特徴とする、洗い流さないタイプの殺菌清浄剤組成物であり、第２の殺菌清浄剤組成物は、（Ａ）カチオン性殺菌剤、（Ｂ−２）ＨＬＢ１０〜１４の一般式（１）で表されるポリオキシエチレン分岐アルキルエーテル及びポリオキシエチレンコレステリルエーテルから選ばれるノニオン性界面活性剤、（Ｃ）アミノ酸又はその塩、及び（Ｄ）炭素数１〜３のアルコール３０〜７０質量％を含有し、フォーマー容器に充填してなり泡状に吐出されることを特徴とする、洗い流さないタイプの殺菌清浄剤組成物である。Hereinafter, the present invention will be described in more detail.
The first bactericidal detergent composition of the present invention comprises (A) a cationic bactericidal agent, (B-1) HLB 9-16 polyoxyethylene hydrogenated castor oil, polyoxyethylene glyceryl monostearate and polyethylene glycol monostearate. A nonionic surfactant selected from (C) an amino acid or a salt thereof, and (D) 16 to 40% by mass of an alcohol having 1 to 3 carbon atoms, filled in a former container, and discharged in a foam form. The second sterilizing detergent composition is characterized by the fact that the second sterilizing detergent composition is (A) a cationic sterilizing agent, (B-2) HLB 10-14 general formula (1) A nonionic surfactant selected from polyoxyethylene branched alkyl ether and polyoxyethylene cholesteryl ether represented by the formula: (C) an amino acid or a salt thereof And (D) a sterilizing detergent composition of a non-washing type characterized by containing 30 to 70% by mass of an alcohol having 1 to 3 carbon atoms, being filled in a former container and discharged in the form of foam. .
（Ａ）カチオン性殺菌剤
カチオン性殺菌剤としては、下記一般式（２）又は（３）で表されるものが挙げられ、１種単独で又は２種以上を併用することができる。(A) Cationic fungicides Examples of the cationic fungicides include those represented by the following general formula (2) or (3), and these can be used alone or in combination of two or more.
一般式（２）で表されるものとしては、塩化ベンザルコニウム、塩化ベンゼトニウム等が挙げられ、一般式（３）で表されるものとしては塩化セチルピリジニウム等が挙げられる。中でも、泡の保形性の点から、塩化ベンザルコニウム、塩化セチルピリジニウムが好ましい。 Examples of the compound represented by the general formula (2) include benzalkonium chloride and benzethonium chloride. Examples of the compound represented by the general formula (3) include cetylpyridinium chloride. Among these, benzalkonium chloride and cetylpyridinium chloride are preferable from the viewpoint of shape retention of bubbles.
（Ａ）成分の配合量（２種以上を併用する場合は合計量）は、殺菌清浄剤組成物中０．０１〜１質量％が好ましく、より好ましくは０．０１〜０．５質量％である。０．０１質量％未満では殺菌性能が不十分となるおそれがあり、１質量％を超えて配合しても殺菌性能として過剰量となったり、手をこすり合わせた後に泡残りをしたりするおそれがある。 (A) The compounding quantity of component (when using 2 or more types together, 0.01-1 mass% is preferable in a disinfection detergent composition, More preferably, it is 0.01-0.5 mass%. is there. If the amount is less than 0.01% by mass, the sterilization performance may be insufficient, and if it exceeds 1% by mass, the amount may be excessive as sterilization performance, or foam may remain after rubbing hands. There is.
（Ｂ−１）ＨＬＢ９〜１６のポリオキシエチレン硬化ヒマシ油、モノステアリン酸ポリオキシエチレングリセリン及びモノステアリン酸ポリエチレングリコールから選ばれるノニオン性界面活性剤
ＨＬＢ９〜１６のポリオキシエチレン硬化ヒマシ油（以下、ポリオキシエチレンをＰＯＥと略す場合がある。）としては、例えば、ポリオキシエチレン（２０）硬化ヒマシ油（ＨＬＢ９）、ポリオキシエチレン（３０）硬化ヒマシ油（ＨＬＢ１１）、ポリオキシエチレン（４０）硬化ヒマシ油（ＨＬＢ１２）、ポリオキシエチレン（５０）硬化ヒマシ油（ＨＬＢ１３）、ポリオキシエチレン（６０）硬化ヒマシ油（ＨＬＢ１４）、ポリオキシエチレン（８０）硬化ヒマシ油（ＨＬＢ１５）、ポリオキシエチレン（１００）硬化ヒマシ油（ＨＬＢ１５）が挙げられる。(B-1) Nonionic surfactant selected from polyoxyethylene hydrogenated castor oil of HLB 9-16, polyoxyethylene glyceryl monostearate and polyethylene glycol monostearate (hereinafter referred to as polyoxyethylene hydrogenated castor oil of HLB 9-16) For example, polyoxyethylene (20) hardened castor oil (HLB9), polyoxyethylene (30) hardened castor oil (HLB11), polyoxyethylene (40) hardened Castor oil (HLB12), polyoxyethylene (50) hydrogenated castor oil (HLB13), polyoxyethylene (60) hydrogenated castor oil (HLB14), polyoxyethylene (80) hydrogenated castor oil (HLB15), polyoxyethylene (100 ) Hardened castor oil (HLB1) 5).
ＨＬＢ９〜１６のモノステアリン酸ポリオキシエチレングリセリンとしては、ポリオキシエチレン（５）グリセリルモノステアレート（以下、ステアリン酸ＰＥＧ-５グリセリル（ＨＬＢ９）と表す。）、ステアリン酸ＰＥＧ-１０グリセリル（ＨＬＢ１１）、ステアリン酸ＰＥＧ-１５グリセリル（ＨＬＢ１３）、ステアリン酸ＰＥＧ-２０グリセリル（ＨＬＢ１４）、ステアリン酸ＰＥＧ-３０グリセリル（ＨＬＢ１５）、ステアリン酸ＰＥＧ-４０グリセリル（ＨＬＢ１６）等が挙げられる。 As polyoxyethylene glycerol monostearate of HLB 9-16, polyoxyethylene (5) glyceryl monostearate (hereinafter referred to as PEG-5 glyceryl stearate (HLB9)), PEG-10 glyceryl stearate (HLB11) PEG-15 glyceryl stearate (HLB13), PEG-20 glyceryl stearate (HLB14), PEG-30 glyceryl stearate (HLB15), PEG-40 glyceryl stearate (HLB16) and the like.
ＨＬＢ９〜１６のモノステアリン酸ポリエチレングリコールとしては、ポリオキシエチレン（１０）モノステアレート（以下、ステアリン酸ＰＥＧ-１０（ＨＬＢ１１）と表す。）、ステアリン酸ＰＥＧ-２０（ＨＬＢ１４）、ステアリン酸ＰＥＧ-３０（ＨＬＢ１５）、ステアリン酸ＰＥＧ-４０（ＨＬＢ１６）が挙げられる。 Examples of polyethylene glycol monostearate of HLB 9-16 include polyoxyethylene (10) monostearate (hereinafter referred to as stearic acid PEG-10 (HLB11)), stearic acid PEG-20 (HLB14), stearic acid PEG- 30 (HLB15) and PEG-40 stearate (HLB16).
本発明のＨＬＢ９〜１６の上記ノニオン性界面活性剤は１種単独で又は２種以上を適宜組み合わせて用いることができる。中でも、ＨＬＢ１２〜１５のポリオキシエチレン硬化ヒマシ油、モノステアリン酸ポリオキシエチレングリセリン、モノステアリン酸ポリエチレングリコールが好ましく、例えば、ポリオキシエチレン（４０）硬化ヒマシ油（ＨＬＢ１２）、ポリオキシエチレン（５０）硬化ヒマシ油（ＨＬＢ１３）、ポリオキシエチレン（６０）硬化ヒマシ油（ＨＬＢ１４）、ポリオキシエチレン（８０）硬化ヒマシ油（ＨＬＢ１５）、ポリオキシエチレン（１００）硬化ヒマシ油（ＨＬＢ１５）、ステアリン酸ＰＥＧ-１５グリセリル（ＨＬＢ１３）、ステアリン酸ＰＥＧ-２０グリセリル（ＨＬＢ１４）、ステアリン酸ＰＥＧ-３０グリセリル（ＨＬＢ１５）、ステアリン酸ＰＥＧ-２０（ＨＬＢ１４）、ステアリン酸ＰＥＧ-３０（ＨＬＢ１５）が挙げられる。（Ｂ−１）のノニオン性界面活性剤においては、ＨＬＢ９未満では、泡の保形性が悪くなり、ＨＬＢ１６を超えても、泡の保形性が悪くなる場合がある。 The said nonionic surfactant of HLB9-16 of this invention can be used individually by 1 type or in combination of 2 or more types. Among them, HLB 12-15 polyoxyethylene hydrogenated castor oil, monostearate polyoxyethylene glycerin, and monostearate polyethylene glycol are preferable. For example, polyoxyethylene (40) hydrogenated castor oil (HLB12), polyoxyethylene (50) Hydrogenated castor oil (HLB13), polyoxyethylene (60) hydrogenated castor oil (HLB14), polyoxyethylene (80) hydrogenated castor oil (HLB15), polyoxyethylene (100) hydrogenated castor oil (HLB15), stearic acid PEG- 15 glyceryl (HLB13), PEG-20 glyceryl stearate (HLB14), PEG-30 glyceryl stearate (HLB15), PEG-20 stearate (HLB14), PEG-30 stearate (HLB15) . In the nonionic surfactant (B-1), if it is less than HLB9, the shape retention of the foam deteriorates, and even if it exceeds HLB16, the shape retention of the foam may deteriorate.
（Ｂ−２）ＨＬＢ１０〜１４の下記一般式（１）で表されるポリオキシエチレン分岐アルキルエーテル及びポリオキシエチレンコレステリルエーテルから選ばれるノニオン性界面活性剤
一般式（１）で表されるポリオキシエチレン分岐アルキルエーテルとしては、例えば下記のものが挙げられる。
ｍ＝６，ｎ＝１０：ポリオキシエチレン（１０）イソセチルエーテル（ＨＬＢ１１）
ｍ＝６，ｎ＝１５：ポリオキシエチレン（１５）イソセチルエーテル（ＨＬＢ１３）
ｍ＝６，ｎ＝２０：ポリオキシエチレン（２０）イソセチルエーテル（ＨＬＢ１４）
ｍ＝７，ｎ＝１０：ポリオキシエチレン（１０）イソステアリルエーテル（ＨＬＢ１１）
ｍ＝７，ｎ＝１５：ポリオキシエチレン（１５）イソステアリルエーテル（ＨＬＢ１２）
ｍ＝７，ｎ＝２０：ポリオキシエチレン（２０）イソステアリルエーテル（ＨＬＢ１３）
ｍ＝７，ｎ＝２５：ポリオキシエチレン（２５）イソステアリルエーテル（ＨＬＢ１４）
ｍ＝８，ｎ＝１０：ポリオキシエチレン（１０）オクチルドデシルエーテル（ＨＬＢ１０）
ｍ＝８，ｎ＝１６：ポリオキシエチレン（１６）オクチルドデシルエーテル（ＨＬＢ１２）
ｍ＝８，ｎ＝２０：ポリオキシエチレン（２０）オクチルドデシルエーテル（ＨＬＢ１３）
ｍ＝８，ｎ＝２５：ポリオキシエチレン（２５）オクチルドデシルエーテル（ＨＬＢ１４）
ｍ＝１０，ｎ＝１５：ポリオキシエチレン（１５）デシルテトラデシルエーテル（ＨＬＢ１１）
ｍ＝１０，ｎ＝２０：ポリオキシエチレン（２０）デシルテトラデシルエーテル（ＨＬＢ１２）
ｍ＝１０，ｎ＝２５：ポリオキシエチレン（２５）デシルテトラデシルエーテル（ＨＬＢ１３）Examples of the polyoxyethylene branched alkyl ether represented by the general formula (1) include the following.
m = 6, n = 10: polyoxyethylene (10) isocetyl ether (HLB11)
m = 6, n = 15: polyoxyethylene (15) isocetyl ether (HLB13)
m = 6, n = 20: polyoxyethylene (20) isocetyl ether (HLB14)
m = 7, n = 10: polyoxyethylene (10) isostearyl ether (HLB11)
m = 7, n = 15: polyoxyethylene (15) isostearyl ether (HLB12)
m = 7, n = 20: polyoxyethylene (20) isostearyl ether (HLB13)
m = 7, n = 25: polyoxyethylene (25) isostearyl ether (HLB14)
m = 8, n = 10: polyoxyethylene (10) octyldodecyl ether (HLB10)
m = 8, n = 16: polyoxyethylene (16) octyldodecyl ether (HLB12)
m = 8, n = 20: polyoxyethylene (20) octyldodecyl ether (HLB13)
m = 8, n = 25: polyoxyethylene (25) octyldodecyl ether (HLB14)
m = 10, n = 15: polyoxyethylene (15) decyl tetradecyl ether (HLB11)
m = 10, n = 20: polyoxyethylene (20) decyl tetradecyl ether (HLB12)
m = 10, n = 25: polyoxyethylene (25) decyl tetradecyl ether (HLB13)
中でも、ＨＬＢ１０〜１３のものが泡の保形性の点で好ましく、具体的には、ポリオキシエチレン（１０）オクチルドデシルエーテル（ＨＬＢ１０）、ポリオキシエチレン（１６）オクチルドデシルエーテル（ＨＬＢ１２）、ポリオキシエチレン（２０）オクチルドデシルエーテル（ＨＬＢ１３）、ポリオキシエチレン（１５）デシルテトラデシルエーテル（ＨＬＢ１１）、ポリオキシエチレン（２０）デシルテトラデシルエーテル（ＨＬＢ１２）、ポリオキシエチレン（２５）デシルテトラデシルエーテル（ＨＬＢ１３）である。（Ｂ−２）のノニオン性界面活性剤においては、ＨＬＢ１０未満では、泡の保形性が悪くなり、ＨＬＢ１４を超えても、泡の保形性が悪くなる場合がある。 Among them, those having HLB of 10 to 13 are preferable from the viewpoint of shape retention of foam. Specifically, polyoxyethylene (10) octyldodecyl ether (HLB10), polyoxyethylene (16) octyldodecyl ether (HLB12), poly Oxyethylene (20) octyldodecyl ether (HLB13), polyoxyethylene (15) decyl tetradecyl ether (HLB11), polyoxyethylene (20) decyl tetradecyl ether (HLB12), polyoxyethylene (25) decyl tetradecyl ether (HLB13). In the nonionic surfactant (B-2), if it is less than HLB10, the shape retention of the foam is deteriorated, and even if it exceeds HLB14, the shape retention of the foam may be deteriorated.
ポリオキシエチレンコレステリルエーテルとしては、ポリオキシエチレンコレステリルエーテルとしては、ポリオキシエチレン（１０）コレステリルエーテル（ＨＬＢ１０）、ポリオキシエチレン（１５）コレステリルエーテル（ＨＬＢ１１）、ポリオキシエチレン（２０）コレステリルエーテル（ＨＬＢ１２）、ポリオキシエチレン（２４）コレステリルエーテル（ＨＬＢ１３）、ポリオキシエチレン（３０）コレステリルエーテル（ＨＬＢ１４）などが挙げられ、中でもポリオキシエチレン（１０）コレステリルエーテル（ＨＬＢ１０）、ポリオキシエチレン（１５）コレステリルエーテル（ＨＬＢ１１）、ポリオキシエチレン（２０）コレステリルエーテル（ＨＬＢ１２）が特に好ましい。なお、（ ）内はエチレンオキシドの平均付加モル数を示す。 As polyoxyethylene cholesteryl ether, polyoxyethylene cholesteryl ether includes polyoxyethylene (10) cholesteryl ether (HLB10), polyoxyethylene (15) cholesteryl ether (HLB11), polyoxyethylene (20) cholesteryl ether (HLB12). ), Polyoxyethylene (24) cholesteryl ether (HLB13), polyoxyethylene (30) cholesteryl ether (HLB14), and the like. Among them, polyoxyethylene (10) cholesteryl ether (HLB10), polyoxyethylene (15) cholesteryl Ether (HLB11) and polyoxyethylene (20) cholesteryl ether (HLB12) are particularly preferred. In addition, the inside of () shows the average addition mole number of ethylene oxide.
なお、ＨＬＢ値とは、界面活性剤を構成している親水基と疎水基の強さのバランスを示す値であり、算出法は下記川上の式による。
ＨＬＢ値＝７＋１１．７ｌｏｇ（ＭW／ＭO）
ＭW：界面活性剤親水部分の分子量
ＭO：界面活性剤親油部分の分子量The HLB value is a value indicating the balance between the strength of the hydrophilic group and the hydrophobic group constituting the surfactant, and the calculation method is based on the following Kawakami equation.
HLB value = 7 + 11.7 log (M W / M O )
M W : Molecular weight of hydrophilic part of surfactant M O : Molecular weight of surfactant lipophilic part
（Ｂ−１）及び（Ｂ−２）成分の配合量（２種以上を併用する場合は合計量）は、殺菌清浄剤組成物中０．０１〜１．０質量％が好ましく、０．１〜０．５質量％が泡の保形性、手をこすり合わせた後の泡残りのなさの点でより好ましい。０．０１質量％未満では、泡の保形性が不十分となるおそれがあり、１．０質量％を超えると使用後にべたつきが生じたり、手をこすり合わせた後の泡残りのなさが劣るおそれがある。 The blending amount of the components (B-1) and (B-2) (the total amount when two or more components are used in combination) is preferably 0.01 to 1.0% by mass in the sterilizing detergent composition. -0.5 mass% is more preferable at the point of the shape retention property of a foam, and the absence of the foam residue after rubbing a hand. If the amount is less than 0.01% by mass, the shape retention of the foam may be insufficient, and if it exceeds 1.0% by mass, stickiness may occur after use or the remaining foam after rubbing hands is inferior. There is a fear.
（Ｃ）アミノ酸又はその塩
本発明のアミノ酸としては、グリシン、リジン、セリン、プロリン、アルギニン、グルタミン酸等、及びピロリドンカルボン酸のアミノ酸誘導体等が挙げられ、これらは１種単独で又は２種以上を適宜組み合わせて用いることができる。塩としては、例えば、アルカリ金属、アルカリ土類金属等が挙げられる。その例として、グルタミン酸ナトリウム、ｄｌ−ピロリドンカルボン酸ナトリウム等が挙げられる。中でも、泡保形性の点から、ｄｌ−ピロリドンカルボン酸ナトリウム、リジン、セリン、グリシンが好ましく、特にｄｌ−ピロリドンカルボン酸ナトリウムが好ましい。(C) Amino acid or salt thereof As the amino acid of the present invention, glycine, lysine, serine, proline, arginine, glutamic acid and the like, and amino acid derivatives of pyrrolidone carboxylic acid, etc., may be used alone or in combination of two or more. They can be used in appropriate combinations. Examples of the salt include alkali metals and alkaline earth metals. Examples thereof include sodium glutamate and sodium dl-pyrrolidonecarboxylate. Of these, sodium dl-pyrrolidonecarboxylate, lysine, serine, and glycine are preferable from the viewpoint of foam shape retention, and sodium dl-pyrrolidonecarboxylate is particularly preferable.
（Ｃ）成分の配合量（２種以上を併用する場合は合計量）は、殺菌清浄剤組成物中０．０１〜５質量％が好ましく、０．１〜１質量％がさらに好ましい。０．０１質量％未満では、手に取った泡が適度な時間で消えづらく、泡残りのなさが劣るおそれがあり、５質量％を超えると吐出時の泡保形性が不十分となるおそれがある。 (C) The compounding quantity of component (when using 2 or more types together, 0.01-5 mass% is preferable in a sterilizing detergent composition, and 0.1-1 mass% is more preferable. If it is less than 0.01% by mass, the foam taken by the hand is difficult to disappear in an appropriate time, and there is a risk that the remaining foam will be inferior. If it exceeds 5% by mass, the foam shape retention at the time of discharge may be insufficient. There is.
（Ｄ）炭素数１〜３のアルコール
炭素数１〜３のアルコールとしては、エチルアルコール、イソプロピルアルコール等が挙げられ、１種単独で又は２種以上を適宜組み合わせて用いることができる。中でも、使用時のにおいの点から、エチルアルコールが好ましい。(D) C1-C3 alcohol As C1-C3 alcohol, ethyl alcohol, isopropyl alcohol, etc. are mentioned, It can use individually by 1 type or in combination of 2 or more types. Among these, ethyl alcohol is preferable from the point of smell at the time of use.
本発明の第１の殺菌清浄剤組成物においては、（Ｄ）成分の配合量（２種以上を併用する場合は合計量）は、殺菌清浄剤組成物中１６〜４０質量％であり、泡の保形性、手をこすり合わせた後の泡残りのなさの点で２０〜３０質量％が好ましい。１６質量％未満では乾きやすさが悪く、また４０質量％を超えると、フォーマー容器から吐出しても泡状にならず、手にとりにくかったり、すぐに液状になり手から垂れてしまうといった不具合が生じる場合がある。 In the first sterilizing detergent composition of the present invention, the blending amount of component (D) (the total amount when two or more are used in combination) is 16 to 40% by mass in the sterilizing detergent composition, and the foam 20-30 mass% is preferable at the point of the shape-retaining property of this, and the absence of the bubble residue after rubbing a hand. If it is less than 16% by mass, it is difficult to dry, and if it exceeds 40% by mass, it does not become foamy even if it is discharged from the former container. May occur.
本発明の第２の殺菌清浄剤組成物においては、（Ｄ）成分の配合量（２種以上を併用する場合は合計量）は、殺菌清浄剤組成物中３０〜７０質量％であり、泡の保形性および手をこすり合わせた後の泡残りのなさという点から、３０〜５０質量％が好ましい。５０質量％以上では、乾きやすさが特に好ましい。３０質量％未満では手をこすり合わせた後も、適度な時間で消泡せず泡残りしてしまう場合があり、また７０質量％を超えると、フォーマー容器から吐出しても泡状にならず、手にとりにくかったり、すぐに液状になり手から垂れてしまうといった不具合が生じる場合がある。 In the 2nd disinfection detergent composition of this invention, the compounding quantity (when using 2 or more types together) of (D) component is 30-70 mass% in disinfection detergent composition, and foam 30 to 50% by mass is preferable from the viewpoint of the shape retention and the absence of bubbles after rubbing hands. When it is 50% by mass or more, easiness of drying is particularly preferable. If the amount is less than 30% by mass, the foam may remain without defoaming in an appropriate time even after the hands are rubbed together. If the amount exceeds 70% by mass, it does not become foamy even if discharged from the former container. In some cases, it may be difficult to handle, or may become liquid and immediately drip from the hand.
本発明の殺菌清浄剤組成物には、本発明の効果を損なわない範囲で任意の成分を配合することができる。任意の成分としては、例えば、多価アルコール等の溶剤、（Ａ）成分及び（Ｄ）成分を除く殺菌剤、水溶性高分子化合物、グリチルリチン酸二カリウム等の消炎剤、香料、清涼剤、冷涼剤、着色料、油分、シリコーン類、ビタミン等の薬剤、ソルビトール、エリスリトール等の糖アルコール、白濁剤、酸化防止剤、金属封鎖剤、動植物抽出物又はその誘導体、無機粉体、粘土鉱物、ナイロン、ポリエチレン等の水不溶性ポリマー粉体、水等が挙げられる。これらは、それぞれ１種単独で又は２種以上を適宜組み合わせて用いることができ、本発明の効果を損なわない範囲で適量配合することができる。 Arbitrary components can be mix | blended with the disinfection detergent composition of this invention in the range which does not impair the effect of this invention. Optional components include, for example, solvents such as polyhydric alcohols, bactericides excluding components (A) and (D), water-soluble polymer compounds, flame retardants such as dipotassium glycyrrhizinate, fragrances, cooling agents, cooling Agents, colorants, oils, silicones, drugs such as vitamins, sugar alcohols such as sorbitol and erythritol, cloudiness agents, antioxidants, sequestering agents, animal and plant extracts or derivatives thereof, inorganic powders, clay minerals, nylon, Examples thereof include water-insoluble polymer powders such as polyethylene and water. These can be used individually by 1 type or in combination of 2 or more types, respectively, and can be blended in an appropriate amount within a range not impairing the effects of the present invention.
多価アルコールとしては、ポリエチレングリコール、１，３−ブチレングリコール、グリセリン等が挙げられ、０〜５質量％配合することが好ましい。多価アルコールの配合で、肌のかさつきを防止できるものの、５質量％を超えて配合すると、使用後に肌のベタつきを生じるおそれがある。 Examples of the polyhydric alcohol include polyethylene glycol, 1,3-butylene glycol, glycerin and the like, and 0 to 5% by mass is preferably blended. Although the blending of the polyhydric alcohol can prevent the skin from becoming thick, if it exceeds 5% by mass, the skin may become sticky after use.
（Ａ）成分及び（Ｄ）成分を除く殺菌剤としては、イソプロピルメチルフェノール、トリクロサン、トリクロロカルバリニド、塩酸クロルヘキシジン、アルキルジアミノエチルグリシン、オクトピロックス等が挙げられる。 Examples of the bactericide excluding the component (A) and the component (D) include isopropylmethylphenol, triclosan, trichlorocarbarinide, chlorhexidine hydrochloride, alkyldiaminoethylglycine, octopirox and the like.
水溶性高分子化合物としては、アクリル酸アルキル共重合体等のアニオン性高分子化合物、カチオン化セルロース、塩化ジメチルジアリルアンモニウム・アクリルアミド共重合体、カチオン変性グアーガム等のカチオン性高分子化合物、ヒドロキシプロピルメチルセルロース、酢酸ビニル・ビニルピロリドン共重合体等のノニオン性高分子化合物、ジメチルアリル４級塩・アクリル酸アクリルアミドビニルピロリドンＮ・Ｎ−ジメチルアミノエチル等の両性ポリマー等が挙げられる。 Examples of water-soluble polymer compounds include anionic polymer compounds such as alkyl acrylate copolymers, cationic polymer compounds such as cationized cellulose, dimethyldiallylammonium chloride / acrylamide copolymer, cation-modified guar gum, and hydroxypropyl methylcellulose. And nonionic polymer compounds such as vinyl acetate / vinyl pyrrolidone copolymer, and amphoteric polymers such as dimethylallyl quaternary salt and acrylamide vinyl pyrrolidone acrylic acid N / N-dimethylaminoethyl.
香料としては、香料成分、香料用溶剤及び香料安定化剤からなる香料組成物を用いることができ、香料組成物の含有量としては、殺菌清浄剤組成物中０．００５〜４０質量％が好ましく、０．０１〜１０質量％がより好ましい。香料成分として使用される香料原料のリストは、様々な文献、例えば、「Ｐｅｒｆｕｍｅ ａｎｄ Ｆｌａｖｏｒ Ｃｈｅｍｉｃａｌｓ」，Ｖｏｌ．Ｉ ａｎｄ ＩＩ，Ｓｔｅｆｆｅｎ Ａｒｃｔａｎｄｅｒ，Ａｌｌｕｒｅｄ Ｐｕｂ．Ｃｏ．（１９９４）；「合成香料化学と商品知識」、印藤元一著、化学工業日報社（１９９６）；「Ｐｅｒｆｕｍｅ ａｎｄ Ｆｌａｖｏｒ Ｍａｔｅｒｉａｌｓ ｏｆ Ｎａｔｕｒａｌ Ｏｒｉｇｉｎ」，Ｓｔｅｆｆｅｎ Ａｒｃｔａｎｄｅｒ，Ａｌｌｕｒｅｄ Ｐｕｂ．Ｃｏ．（１９９４）；「香りの百科」、日本香料協会編、朝倉書店（１９８９）；「Ｐｅｒｆｕｍｅｒｙ Ｍａｔｅｒｉａｌ Ｐｅｒｆｏｒｍａｎｃｅ Ｖ．３．３」，Ｂｏｅｌｅｎｓ Ａｒｏｍａ Ｃｈｅｍｉｃａｌ Ｉｎｆｏｒｍａｔｉｏｎ Ｓｅｒｖｉｃｅ（１９９６）；「Ｆｌｏｗｅｒ ｏｉｌｓ ａｎｄ Ｆｌｏｒａｌ Ｃｏｍｐｏｕｎｄｓ Ｉｎ Ｐｅｒｆｕｍｅｒｙ」，Ｄａｎｕｔｅ Ｌａｊａｕｊｉｓ Ａｎｏｎｉｓ，Ａｌｌｕｒｅｄ Ｐｕｂ．Ｃｏ．（１９９３）等に挙げられており、例えば、これらの文献に記載された香料原料の中から、前記香料成分を適宜選択することができる。具体的には、例えば、ユーカリ油、カンフル、ボルネオール、レモン油、ライム油、グレープフルーツエキス、ラベンダー油、ラベンダーエキス、ローズマリー油、ローズマリーエキス等が挙げられる。 As the fragrance, a fragrance composition comprising a fragrance component, a fragrance solvent and a fragrance stabilizer can be used, and the content of the fragrance composition is preferably 0.005 to 40% by mass in the sterilizing detergent composition. 0.01 to 10% by mass is more preferable. A list of perfume ingredients used as perfume ingredients can be found in various publications such as “Perfume and Flavor Chemicals”, Vol. I and II, Stephen Arctander, Allured Pub. Co. (1994); “Synthetic perfume chemistry and commercial knowledge”, Motoichi Into, Chemical Industry Daily (1996); “Perfume and Flavor Materials of Natural Origin”, Stephen Arctander, Allred Pub. Co. (1994); "Encyclopedia of Scents", edited by Japan Fragrance Association, Asakura Shoten (1989); "Perfume Material Materials Performance V.3.3", Boelens Aroma Chemical Information Service (1996); "Flower oils". , Danute Lajaujis Anonis, Allured Pub. Co. (1993) etc. For example, the said fragrance | flavor component can be suitably selected from the fragrance | flavor raw materials described in these literature. Specific examples include eucalyptus oil, camphor, borneol, lemon oil, lime oil, grapefruit extract, lavender oil, lavender extract, rosemary oil, rosemary extract and the like.
香料用溶剤としては、例えば、エタノール、ベンジルベンゾエート、アセチン（トリアセチン）、ＭＭＢアセテート（３−メトキシ−３−メチルブチルアセテート）、エチレングリコールジブチレート、ヘキシレングリコール、ジブチルセバケート、デルチールエキストラ（イソプロピルミリステート）、メチルカルビトール（ジエチレングリコールモノメチルエーテル）、カルビトール（ジエチレングリコールモノエチルエーテル）、ＴＥＧ（トリエチレングリコール）、安息香酸ベンジル、プロピレングリコール、フタル酸ジエチル、トリプロピレングリコール、アボリン（ジメチルフタレート）、デルチルプライム（イソプロピルパルミテート）、ジプロピレングリコールＤＰＧ−ＦＣ（ジプロピレングリコール）、ファルネセン、ジオクチルアジペート、トリブチリン（グリセリルトリブタノエート）、ヒドロライト−５（１，２−ペンタンジオール）、プロピレングリコールジアセテート、セチルアセテート（ヘキサデシルアセテート）、エチルアビエテート、アバリン（メチルアビエテート）、シトロフレックスＡ−２（アセチルトリエチルシトレート）、シトロフレックスＡ−４（トリブチルアセチルシトレート）、シトロフレックスＮｏ．２（トリエチルシトレート）、シトロフレックスＮｏ．４（トリブチルシトレート）、ドゥラフィックス（メチルジヒドロアビエテート）、ＭＩＴＤ（イソトリデシルミリステート）、ポリリモネン（リモネンポリマー）、１，３−ブチレングリコール等が挙げられる。香料用溶剤の含有量としては、香料組成物中０．１〜９９質量％が好ましく、０．１〜１０質量％がより好ましい。 Examples of the perfume solvent include ethanol, benzyl benzoate, acetin (triacetin), MMB acetate (3-methoxy-3-methylbutyl acetate), ethylene glycol dibutyrate, hexylene glycol, dibutyl sebacate, deltile extra (isopropyl). Myristate), methyl carbitol (diethylene glycol monomethyl ether), carbitol (diethylene glycol monoethyl ether), TEG (triethylene glycol), benzyl benzoate, propylene glycol, diethyl phthalate, tripropylene glycol, aboline (dimethyl phthalate), Deltyl prime (isopropyl palmitate), dipropylene glycol DPG-FC (dipropylene glycol), farnesene, di Cutyl adipate, tributyrin (glyceryl tributanoate), hydrolite-5 (1,2-pentanediol), propylene glycol diacetate, cetyl acetate (hexadecyl acetate), ethyl abiate, avaline (methyl abiate), citroflex A-2 (acetyl triethyl citrate), Citroflex A-4 (tributyl acetyl citrate), Citroflex No. 2 (triethyl citrate), Citroflex No. 4 (tributyl citrate), Durafix (methyl dihydroabietate), MITD (isotridecyl myristate), polylimonene (limonene polymer), 1,3-butylene glycol and the like. As content of the solvent for fragrance | flavors, 0.1-99 mass% is preferable in a fragrance | flavor composition, and 0.1-10 mass% is more preferable.
香料安定化剤としては、例えば、ジブチルヒドロキシトルエン、ブチルヒドロキシアニソール、ビタミンＥとその誘導体、カテキン化合物、フラボノイド化合物、ポリフェノール化合物等が挙げられ、中でも、ジブチルヒドロキシトルエンが好ましい。香料安定化剤の含有量としては、香料組成物中０．０００１〜１０質量％が好ましく、０．００１〜５質量％がより好ましい。 Examples of the fragrance stabilizer include dibutylhydroxytoluene, butylhydroxyanisole, vitamin E and its derivatives, catechin compounds, flavonoid compounds, polyphenol compounds, etc. Among them, dibutylhydroxytoluene is preferable. As content of a fragrance | flavor stabilizer, 0.0001-10 mass% is preferable in a fragrance | flavor composition, and 0.001-5 mass% is more preferable.
清涼剤としては、メントール、ペパーミント油、ハッカ油等が挙げられる。具体的には、Ｎ−エチルパラメンタンカルボキサミド（商品名：ＷＳ３）、ｌ−メンチルグリセリルエーテル（商品名：ＣＡ−１０）、メンチルラクテート（商品名：ＦｒｅｓｃｏｌａｔＭＬ，ＦｒｅｓｃｏｌａｔＭＧＡ）等が挙げられる。 Examples of the refreshing agent include menthol, peppermint oil, mint oil and the like. Specifically, N-ethyl paramentane carboxamide (trade name: WS3), l-menthyl glyceryl ether (trade name: CA-10), menthyl lactate (trade names: Frescolat ML, Frescolat MGA) and the like can be mentioned.
本発明の殺菌清浄剤組成物の製造方法としては、上記必須成分、任意成分、及び水（残部）を混合すればよく、特に制限はなく、目的に応じて適宜選択することができる。また、殺菌清浄剤組成物を調製する装置としては特に制限はなく、目的に応じて適宜選択することができ、剪断力と全体混合できる複数の攪拌羽根（プロペラ、タービン、ディスパー等）を備えた攪拌装置が好ましい。殺菌清浄剤組成物の原料としては特に制限はなく、目的に応じて適宜選択することができる。また、それぞれの原料を単独で使用してもよく、それぞれの原料を含む混合物を使用してもよい。 As a manufacturing method of the sterilizing detergent composition of this invention, the said essential component, arbitrary components, and water (remainder) should just be mixed, there is no restriction | limiting in particular and it can select suitably according to the objective. Moreover, there is no restriction | limiting in particular as an apparatus which prepares a disinfection detergent composition, According to the objective, it can select suitably, It was equipped with the several stirring blade (propeller, turbine, disper, etc.) which can mix with a shear force and the whole. A stirrer is preferred. There is no restriction | limiting in particular as a raw material of a disinfection detergent composition, According to the objective, it can select suitably. Moreover, each raw material may be used independently and the mixture containing each raw material may be used.
本発明の殺菌清浄剤組成物のｐＨは４〜７が好ましい。皮膚マイルド性の点からこの範囲が好ましく、ｐＨ７を超えると防腐力が劣るおそれがある。ｐＨの調整には、クエン酸とクエン酸ナトリウムを用いることが好ましい。なお、本発明のｐＨは、２５℃で、ｐＨメーター（東亜電波工業製ＨＭ−３０Ｇ）、ｐＨ電極（東亜ディーケーケー（株）製ＧＳＴ−５７２１Ｃ型）を用いて測定した値である。 The pH of the sterilizing detergent composition of the present invention is preferably 4-7. This range is preferable from the point of skin mildness, and when it exceeds pH 7, antiseptic power may be inferior. To adjust the pH, it is preferable to use citric acid and sodium citrate. The pH of the present invention is a value measured at 25 ° C. using a pH meter (HM-30G manufactured by Toa Denpa Kogyo Co., Ltd.) and a pH electrode (GST-5721C manufactured by Toa DKK Co., Ltd.).
本発明の殺菌清浄剤組成物は常温で液体状であり、使用する温度条件下で殺菌清浄剤組成物の粘度は、３０ｍＰａ・ｓ以下が好ましく、１０ｍＰａ・ｓ以下がより好ましい。なお、本発明の粘度は温度（使用する温度条件、通常２５℃）で、回転粘度計（東京計器（株）製、型式Ｂ８Ｌ）を用い、Ｎｏ．１ローター回転数６０ｒｐｍにて６０秒測定した値である。 The sterilizing detergent composition of the present invention is liquid at normal temperature, and the viscosity of the sterilizing detergent composition is preferably 30 mPa · s or less, more preferably 10 mPa · s or less, under the temperature conditions used. The viscosity of the present invention is a temperature (temperature condition to be used, usually 25 ° C.), and a rotational viscometer (manufactured by Tokyo Keiki Co., Ltd., model B8L) is used. It is a value measured for 60 seconds at 1 rotor rotation speed 60 rpm.
本発明の殺菌清浄剤組成物は、フォーマー容器に充填してなり泡状に吐出される、洗い流さないタイプのものである。泡状であることから、ゲル状やスプレー状のものよりも使いやすく、水のないところで簡単に殺菌・洗浄を行うことができる。また、洗い流さないタイプの殺菌清浄剤組成物と、これを収容し泡状に吐出させるフォーマー容器とを備える殺菌清浄剤製品とすることもできる。 The sterilizing detergent composition of the present invention is of a type that is filled in a former container and discharged in the form of a foam and is not washed off. Since it is foamy, it is easier to use than gels and sprays, and can be easily sterilized and washed in the absence of water. Moreover, it can also be set as the sterilization detergent product provided with the sterilization detergent composition of the type which is not washed away, and the former container which accommodates this and discharges in foam form.
フォーマー容器としては、ノンガス型の泡吐出容器、噴射剤と耐圧容器を使用したエアゾール容器が挙げられるが、ノンガス型の泡吐出容器が好ましい。ノンガス型の泡吐出容器としては、殺菌清浄剤組成物を空気と混合して発泡状態で吐出できるものであれば特に限定されず、例えば、ボトル胴部を手で圧搾することによって泡を吐出できるスクイズフォーマー容器、ノズル部を押し下げることによって泡を吐出できるポンプフォーマー容器等が挙げられ、目的に応じて適宜選択することができる。このようなフォーマー容器は、大和製罐株式会社製、株式会社吉野工業所製等のものを使用することができる。より具体的には、フォーマー容器としては、特開平７−３１５４６３号公報、特開平８−２３０９６１号公報、及び特開２００５−１９３９７２号公報に記載されたフォーマー容器等を使用することができる。 Examples of the former container include a non-gas type foam discharge container and an aerosol container using a propellant and a pressure-resistant container, and a non-gas type foam discharge container is preferable. The non-gas type foam discharge container is not particularly limited as long as the sterilizing detergent composition can be mixed with air and discharged in a foamed state. For example, foam can be discharged by manually squeezing the bottle body. Examples thereof include a squeeze foamer container and a pump foamer container that can discharge bubbles by depressing the nozzle part, and can be appropriately selected according to the purpose. As such a former container, those made by Yamato Steel Co., Ltd., Yoshino Kogyo Co., Ltd., etc. can be used. More specifically, the former container described in JP-A-7-315463, JP-A-8-230961, and JP-A-2005-193972 can be used as the former container.
ノンガス型の泡吐出容器は泡形成部材を有し、具体的には、泡を形成するための多孔質膜体（材質はナイロン、ポリエステル、ポリオレフィン等のプラスチック材料が好ましい）を有し、殺菌清浄剤組成物が該多孔質膜体を通過することにより泡が形成されるものである。多孔質膜体のメッシュとしては、特に制限はなく、目的に応じて適宜選択することができ、例えば、１００メッシュ以上が好ましく、１００〜４００メッシュがより好ましく、２００〜３０５メッシュが特に好ましい。また、多孔質膜体の枚数としては特に制限はなく、目的に応じて適宜選択することができ、泡性能を向上させる観点から２〜４枚が好ましい。より具体的には、特開平７−３１５４６３号公報、特開平８−２３０９６１号公報、及び特開２００５−１９３９７２号公報に記載されたフォーマー容器を好適に使用することができる。例えば、ノズル部を押し下げることによって泡を吐出できるポンプフォーマー容器と３０５、２００メッシュ各１枚使用する際において、使用する温度条件下で殺菌清浄剤組成物の粘度は、３０ｍＰａ・ｓ以下が好ましく、１０ｍＰａ・ｓ以下がより好ましい。 The non-gas type foam discharge container has a foam forming member, specifically, has a porous film body for forming foam (material is preferably a plastic material such as nylon, polyester, polyolefin, etc.) and is sterilized and cleaned. Bubbles are formed by the agent composition passing through the porous membrane. There is no restriction | limiting in particular as a mesh of a porous membrane body, According to the objective, it can select suitably, For example, 100 mesh or more are preferable, 100-400 mesh is more preferable, 200-305 mesh is especially preferable. Moreover, there is no restriction | limiting in particular as the number of sheets of a porous membrane body, It can select suitably according to the objective, and 2-4 sheets are preferable from a viewpoint of improving foam performance. More specifically, the former containers described in JP-A-7-315463, JP-A-8-230961, and JP-A-2005-193972 can be preferably used. For example, when using a pump former container capable of discharging bubbles by pushing down the nozzle and one each of 305 and 200 mesh, the viscosity of the sterilizing detergent composition is preferably 30 mPa · s or less under the temperature conditions used. 10 mPa · s or less is more preferable.
本発明において、洗い流さないタイプとは、泡状の殺菌清浄剤組成物を手にとり、殺菌清浄対象、例えば手、全身等の皮膚に広げた後、水等で洗い流さずに使用するものをいう。使用方法としては特に限定されないが、１日数回、適量１〜１５ｇを泡状にして手にとり、殺菌清浄対象、例えば手、全身等にいきわたらせる方法等が挙げられる。 In the present invention, the type that does not wash away means a foam-like sterilizing detergent composition that is used without being washed away with water after being spread on a sterilized and clean target, for example, the skin of a hand or the whole body. Although it does not specifically limit as a usage method, The method etc. etc. etc. which are suitable for a sterilization cleaning object, for example, a hand, the whole body, etc. are taken several times a day, taking a suitable amount 1-15g in the shape of a foam.
以下、実施例及び比較例を示し、本発明を具体的に説明するが、本発明は下記の実施例に制限されるものではない。なお、下記の例において特に明記のない場合は、組成の「％」は質量％、比率は質量比を示し、実施例記載の成分量は全て純分換算である。 EXAMPLES Hereinafter, although an Example and a comparative example are shown and this invention is demonstrated concretely, this invention is not restrict | limited to the following Example. In the following examples, unless otherwise specified, “%” in the composition represents mass%, the ratio represents the mass ratio, and all the component amounts described in the examples are in terms of pure matter.
［実施例１〜６７、比較例１〜１７］
表１〜１４に示す組成の殺菌清浄剤組成物を常法に準じて調製し、組成物のｐＨを約５．６に調整した。実施例の殺菌清浄剤組成物の粘度（２５℃）を、回転粘度計（東京計器（株）製、型式Ｂ８Ｌ）を用い、Ｎｏ．１ローター回転数６０ｒｐｍにて６０秒測定したところ、１〜９ｍＰａ・ｓであった。得られた殺菌清浄剤組成物２５０ｍＬのフォーマー容器に２００ｇ充填した。このフォーマー容器のスペックは特開２００５−１９３９７２号公報に記載された方法に準じ、商品名Ｗ−５７２１、ＷＰ．ＦＴ Ｌノズル（吉野工業所製）のものを使用した。具体的には、気／液の容積比：１３／１、吐出量：１ｇ（１プッシュ）、口径は５ｍｍ×８ｍｍ（楕円状）、泡形成部材：２００メッシュと３０５メッシュの多孔質膜体各１枚ずつのものを用いた。[Examples 1 to 67, Comparative Examples 1 to 17]
The sterilizing detergent compositions having the compositions shown in Tables 1 to 14 were prepared according to a conventional method, and the pH of the composition was adjusted to about 5.6. The viscosity (25 ° C.) of the sterilizing detergent composition of Examples was measured using a rotational viscometer (manufactured by Tokyo Keiki Co., Ltd., model B8L). It was 1-9 mPa * s when it measured for 60 second at 1 rotor rotation speed 60rpm. 200 g of the resulting sterilizing detergent composition 250 mL former container was filled. The specifications of this former container are in accordance with the method described in JP-A-2005-193972, and trade names W-5721, WP. An FT L nozzle (manufactured by Yoshino Kogyo) was used. Specifically, gas / liquid volume ratio: 13/1, discharge amount: 1 g (1 push), caliber 5 mm × 8 mm (elliptical), foam forming member: 200 mesh and 305 mesh porous film bodies One by one was used.
[泡の保形性]
２５℃・６０％ＲＨの条件下で、ポリ塩化ビニリデンフィルム上に、フォーマー容器から泡状の殺菌清浄剤組成物１ｇを吐出させ、吐出３０秒後の泡高さを測定した。この評価方法において、５ｍｍ未満のものは泡の保形性が悪く手に取ったときに垂れやすく、２０ｍｍ以上の場合は、手に取った泡が適度な時間で消えず、手に擦り込みにくい。すなわち、使用性上好ましい泡保形性及び適度な消泡時間としては、この評価方法で、５ｍｍ以上２０ｍｍ未満のものである。結果は、３回測定した平均値に基づき、以下の判定基準でしめした。
〈判定基準〉
◎：１６ｍｍ以上２０ｍｍ未満
○：１３ｍｍ以上１６ｍｍ未満
△：５ｍｍ以上１３ｍｍ未満
×：５ｍｍ未満又は２０ｍｍ以上[Foam shape retention]
Under conditions of 25 ° C. and 60% RH, 1 g of a foam-like sterilizing detergent composition was discharged from a former container onto a polyvinylidene chloride film, and the foam height after 30 seconds from the discharge was measured. In this evaluation method, those with a diameter of less than 5 mm have poor shape retention of the foam and are easy to sag when picked up, and when it is 20 mm or more, the foam taken up by the hand does not disappear in an appropriate time and is not easily rubbed into the hand. That is, the preferable foam shape-retaining property and the appropriate defoaming time in terms of usability are 5 mm or more and less than 20 mm in this evaluation method. The results were shown by the following criteria based on the average value measured three times.
<Criteria>
◎: 16 mm or more and less than 20 mm ○: 13 mm or more and less than 16 mm Δ: 5 mm or more and less than 13 mm x: less than 5 mm or 20 mm or more
[手をこすり合わせた後の泡残りのなさ]
２５℃・６０％ＲＨの条件下で、フォーマー容器から泡状の殺菌清浄剤組成物１ｇを、手に吐出させ、約１０秒間手をこすり合わせた後、手のひら上の泡残りを評価した。結果は、専門パネル１０名が下記評点で官能評価し、その評点の平均値に基づき、下記判定基準で示した。
〈評点〉
５点：全く泡残りがない（許容範囲内）
４点：ほとんど泡残りがない（許容範囲内）
３点：やや泡残りがある（許容範囲内）
２点：かなり泡残りがある（許容範囲外）
１点：泡が増えてくる（許容範囲外）
〈判定基準〉
◎：４．０以上
○：３．０以上４．０未満
△：２．０以上３．０未満
×：２．０未満[No bubbles left after rubbing hands]
Under the conditions of 25 ° C. and 60% RH, 1 g of a foam-like sterilizing detergent composition was discharged from the former container and rubbed hands for about 10 seconds, and then the foam residue on the palm was evaluated. The results were shown by the following criteria based on the sensory evaluation of 10 professional panels based on the following scores and the average of the scores.
<Score>
5 points: No bubble residue (within tolerance)
4 points: almost no foam residue (within tolerance)
3 points: Some bubble residue (within tolerance)
2 points: There is considerable foam residue (out of tolerance)
1 point: Bubbles increase (out of tolerance)
<Criteria>
◎: 4.0 or more ○: 3.0 or more and less than 4.0 Δ: 2.0 or more and less than 3.0 ×: less than 2.0
[乾きやすさ]
２５℃・６０％ＲＨの条件下で、フォーマー容器から泡状の殺菌清浄剤組成物１ｇを、手に吐出させ、手及び手の甲にすり込みながら液が乾くまでの時間を測定した。結果は、専門パネル１０名が官能評価し、その時間の平均値に基づき、下記判定基準で示した。
〈判定基準〉
◎：３０秒未満（許容範囲内）
○：３０秒以上６０秒未満（許容範囲内）
△：６０秒以上９０秒未満（許容範囲外）
×：９０秒以上（許容範囲外）[Ease of drying]
Under the conditions of 25 ° C. and 60% RH, 1 g of the foamy sterilizing detergent composition was discharged from the former container into the hand, and the time until the liquid dried was measured while being rubbed into the hand and back of the hand. The results were sensory-evaluated by 10 professional panels, and the following criteria were used based on the average value of the time.
<Criteria>
A: Less than 30 seconds (within allowable range)
○: 30 seconds or more and less than 60 seconds (within allowable range)
Δ: 60 seconds or more and less than 90 seconds (outside the allowable range)
×: 90 seconds or more (outside the allowable range)
[殺菌力（減菌率（％）]
一方の手の３本指を標準寒天培地（日本製薬（株）製）にプレーティングして使用前の菌を採取した。その後、他方の手に殺菌清浄剤組成物１ｇを採り、液が乾くまで手指にすりこんだ後、標準寒天培地に３本指をプレーティングし、使用後の菌を採取した（ストリークプレート法）。殺菌清浄剤組成物使用前後の手指の菌を、３７℃で２４時間培養した後コロニー数を測定した。以下の式に従って、使用前コロニー数Ａ0、使用後コロニー数Ａ1から減菌率を示した。減菌率９５％以上のものが有効であり、７０％未満は無効である。
減菌率（％）＝（１−Ａ1／Ａ0）×１００[Bactericidal power (Bacteria sterilization rate (%)]
Three fingers of one hand were plated on a standard agar medium (manufactured by Nippon Pharmaceutical Co., Ltd.) to collect the bacteria before use. Thereafter, 1 g of the sterilizing detergent composition was taken in the other hand, rubbed into the fingers until the solution was dry, and then three fingers were plated on a standard agar medium, and the used bacteria were collected (streak plate method) . The bacteria of the fingers before and after using the sterilizing detergent composition were cultured at 37 ° C. for 24 hours, and then the number of colonies was measured. According to the following formula, the sterilization rate was shown from the number of colonies A 0 before use and the number of colonies A 1 after use. A sterilization rate of 95% or more is effective, and less than 70% is invalid.
Sterilization rate (%) = (1−A 1 / A 0 ) × 100
＊２：アルキル鎖長（Ｒ2）はＣ１６
＊３：エーテル結合を有する炭化水素基（Ｒ1）はＣ18Ｈ29Ｏ2
* 2: Alkyl chain length (R 2 ) is C16
* 3: The hydrocarbon group having an ether bond (R 1 ) is C 18 H 29 O 2
＊２：アルキル鎖長（Ｒ2）はＣ１６
* 2: Alkyl chain length (R 2 ) is C16
＊２：アルキル鎖長（Ｒ2）はＣ１６
＊３：エーテル結合を有する炭化水素基（Ｒ1）はＣ18Ｈ29Ｏ2
* 2: Alkyl chain length (R 2 ) is C16
* 3: The hydrocarbon group having an ether bond (R 1 ) is C 18 H 29 O 2
＊２：アルキル鎖長（Ｒ2）はＣ１６
＊３：エーテル結合を有する炭化水素基（Ｒ1）はＣ18Ｈ29Ｏ2
* 2: Alkyl chain length (R 2 ) is C16
* 3: The hydrocarbon group having an ether bond (R 1 ) is C 18 H 29 O 2
＊２：アルキル鎖長（Ｒ2）はＣ１６
* 2: Alkyl chain length (R 2 ) is C16
［実施例６８］
下記の組成に従い、常法により実施例６８の全身用殺菌清浄剤組成物を調製した。得られた全身用殺菌清浄剤組成物について、実施例１と同様にフォーマー容器に充填し、同様に評価を行った。（ｐＨ５．６、粘度（２５℃）、４ｍＰａ・ｓ）
泡の保形性：◎
手をこすり合わせた後の泡残りのなさ：◎
乾きやすさ：○
減菌率：９９％[Example 68]
According to the following composition, the whole body sterilizing detergent composition of Example 68 was prepared by a conventional method. About the obtained bactericidal detergent composition for whole body, it filled with the former container similarly to Example 1, and evaluated similarly. (PH 5.6, viscosity (25 ° C.), 4 mPa · s)
Foam shape retention: ◎
No remaining foam after rubbing hands: ◎
Ease of drying: ○
Sterilization rate: 99%
実施例及び比較例を調製する際に用いた原料を以下に示す。
（１）塩化ベンザルコニウム：日油（株）製，ニッサンカチオンＦ２−５０Ｅ
＊１：アルキル鎖長（Ｒ1）は、Ｃ１２／Ｃ１４＝６３／３７（質量比）
（２）塩化セチルピリジニウム：和光純薬工業（株）製，塩化セチルピリジニウム
＊２：アルキル鎖長（Ｒ2）は、Ｃ１６
（３）塩化ベンゼトニウム：三菱化学フーズ（株）製 ハイアミン結晶
＊３：エーテル結合を有する炭化水素基（Ｒ1）はＣ18Ｈ29Ｏ2
（４）ポリオキシエチレン（２０）硬化ヒマシ油（ＰＥＧ−２０硬化ヒマシ油）：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＨＣ−２０
（５）ポリオキシエチレン（４０）硬化ヒマシ油（ＰＥＧ−４０硬化ヒマシ油）：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＨＣ−４０
（６）ポリオキシエチレン（６０）硬化ヒマシ油（ＰＥＧ−６０硬化ヒマシ油）：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＨＣ−６０
（７）ポリオキシエチレン（１００）硬化ヒマシ油（ＰＥＧ−１００硬化ヒマシ油）：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＨＣ−１００
（８）ステアリン酸ＰＥＧ-１０：日本エマルジョン（株）製，ＥＭＡＬＥＸ８１０
（９）ステアリン酸ＰＥＧ-２０：日本エマルジョン（株）製，ＥＭＡＬＥＸ８２０
（１０）ステアリン酸ＰＥＧ-４０：日本エマルジョン（株）製，ＥＭＡＬＥＸ８４０
（１１）ステアリン酸ＰＥＧ-１０グリセリル：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＧＭ-１０
（１２）ステアリン酸ＰＥＧ-１５グリセリル：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＧＭ-１５
（１３）ステアリン酸ＰＥＧ-４０グリセリル：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＧＭ-４０
（１４）ｄｌ−ピロリドンカルボン酸ナトリウム 味の素（株）製，ＰＣＡソーダ
（１５）リジン：味の素（株）製，塩酸Ｌ−リジン
（１６）セリン：協和発酵工業（株）製，Ｌ−セリン
（１７）ポリオキシエチレン（１０）硬化ヒマシ油（ＰＥＧ−１０硬化ヒマシ油）：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＨＣ−１０
（１８）ステアリン酸ＰＥＧ-１５０：日本エマルジョン（株）製，ＥＭＡＬＥＸ ６３００Ｍ-ＳＴ
（１９）イミダゾリニウムベタイン：東邦化学工業（株）製，オバゾリン６６２Ｎ
（２０）ポリオキシエチレン（１０）コレステリルエーテル：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＣＳ-１０
（２１）ポリオキシエチレン（１５）デシルテトラデシルエーテル：日本エマルジョン（株）製，ＥＭＡＬＥＸ ２４１５
（２２）ポリオキシエチレン（１０）オクチルドデシルエーテル：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＯＤ-１０
（２３）ポリオキシエチレン（２０）オクチルドデシルエーテル：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＯＤ-２０
（２４）ポリオキシエチレン（２５）オクチルドデシルエーテル：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＯＤ-２５
（２５）ポリオキシエチレン（５）コレステリルエーテル：日本エマルジョン（株）製，ＥＭＡＬＥＸ ＣＳ-５
（２６）ポリオキシエチレン（１０）デシルテトラデシルエーテル：日本エマルジョン（株）製，ＥＭＡＬＥＸ ２４１０
（２７）ポリオキシエチレン（２０）イソセチルエーテル：日本エマルジョン（株）製，ＥＭＡＬＥＸ １６２０The raw materials used in preparing the examples and comparative examples are shown below.
(1) Benzalkonium chloride: manufactured by NOF Corporation, Nissan Cation F2-50E
* 1: Alkyl chain length (R 1 ) is C12 / C14 = 63/37 (mass ratio)
(2) Cetylpyridinium chloride: manufactured by Wako Pure Chemical Industries, Ltd., cetylpyridinium chloride * 2: alkyl chain length (R 2 ) is C16
(3) Benzethonium chloride: manufactured by Mitsubishi Chemical Foods Corporation High amine crystal * 3: The hydrocarbon group (R 1 ) having an ether bond is C 18 H 29 O 2
(4) Polyoxyethylene (20) hydrogenated castor oil (PEG-20 hydrogenated castor oil): manufactured by Nippon Emulsion Co., Ltd., EMALEX HC-20
(5) Polyoxyethylene (40) hydrogenated castor oil (PEG-40 hydrogenated castor oil): manufactured by Nippon Emulsion Co., Ltd., EMALEX HC-40
(6) Polyoxyethylene (60) hydrogenated castor oil (PEG-60 hydrogenated castor oil): manufactured by Nippon Emulsion Co., Ltd., EMALEX HC-60
(7) Polyoxyethylene (100) hydrogenated castor oil (PEG-100 hydrogenated castor oil): manufactured by Nippon Emulsion Co., Ltd., EMALEX HC-100
(8) PEG-10 stearate: manufactured by Nippon Emulsion Co., Ltd., EMALEX810
(9) PEG-20 stearate: manufactured by Nippon Emulsion Co., Ltd., EMALEX820
(10) PEG-40 stearate: manufactured by Nippon Emulsion Co., Ltd., EMALEX 840
(11) PEG-10 glyceryl stearate: manufactured by Nippon Emulsion Co., Ltd., EMALEX GM-10
(12) PEG-15 stearate glyceryl: manufactured by Nippon Emulsion Co., Ltd., EMALEX GM-15
(13) PEG-40 glyceryl stearate: manufactured by Nippon Emulsion Co., Ltd., EMALEX GM-40
(14) Sodium dl-pyrrolidonecarboxylate Ajinomoto Co., Inc., PCA soda (15) Lysine: Ajinomoto Co., Ltd., L-lysine hydrochloride (16) Serine: Kyowa Hakko Kogyo Co., Ltd., L-Serine (17 ) Polyoxyethylene (10) hydrogenated castor oil (PEG-10 hydrogenated castor oil): manufactured by Nippon Emulsion Co., Ltd., EMALEX HC-10
(18) PEG-150 stearate: manufactured by Nippon Emulsion Co., Ltd., EMALEX 6300M-ST
(19) Imidazolinium betaine: Obazoline 662N manufactured by Toho Chemical Industry Co., Ltd.
(20) Polyoxyethylene (10) cholesteryl ether: manufactured by Nippon Emulsion Co., Ltd., EMALEX CS-10
(21) Polyoxyethylene (15) decyltetradecyl ether: manufactured by Nippon Emulsion Co., Ltd., EMALEX 2415
(22) Polyoxyethylene (10) octyldodecyl ether: manufactured by Nippon Emulsion Co., Ltd., EMALEX OD-10
(23) Polyoxyethylene (20) octyldodecyl ether: manufactured by Nippon Emulsion Co., Ltd., EMALEX OD-20
(24) Polyoxyethylene (25) octyldodecyl ether: manufactured by Nippon Emulsion Co., Ltd., EMALEX OD-25
(25) Polyoxyethylene (5) cholesteryl ether: manufactured by Nippon Emulsion Co., Ltd., EMALEX CS-5
(26) Polyoxyethylene (10) decyltetradecyl ether: manufactured by Nippon Emulsion Co., Ltd., EMALEX 2410
(27) Polyoxyethylene (20) isocetyl ether: manufactured by Nippon Emulsion Co., Ltd., EMALEX 1620
Claims (3)
で表されるポリオキシエチレン分岐アルキルエーテル及びポリオキシエチレンコレステリルエーテルから選ばれるノニオン性界面活性剤、（Ｃ）アミノ酸又はその塩、及び（Ｄ）炭素数１〜３のアルコール３０〜７０質量％を含有し、フォーマー容器に充填してなり泡状に吐出されることを特徴とする、洗い流さないタイプの殺菌清浄剤組成物。(A) Cationic fungicide, (B-2) HLB 10-14, following general formula (1)
A nonionic surfactant selected from polyoxyethylene branched alkyl ether and polyoxyethylene cholesteryl ether represented by: (C) an amino acid or a salt thereof, and (D) 30 to 70% by mass of an alcohol having 1 to 3 carbon atoms. A sterilizing detergent composition of a non-washing type, characterized in that it is contained, filled in a former container and discharged in the form of foam.
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| JP2009545367A JP5343857B2 (en) | 2007-12-12 | 2008-10-27 | Bactericidal detergent composition |
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| JP2007320531 | 2007-12-12 | ||
| JP2009545367A JP5343857B2 (en) | 2007-12-12 | 2008-10-27 | Bactericidal detergent composition |
| PCT/JP2008/069407 WO2009075142A1 (en) | 2007-12-12 | 2008-10-27 | Bactericidal cleanser composition |
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| JP (1) | JP5343857B2 (en) |
| KR (1) | KR101443951B1 (en) |
| CN (1) | CN101896595B (en) |
| HK (1) | HK1145511A1 (en) |
| MY (1) | MY155282A (en) |
| WO (1) | WO2009075142A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2017226766A (en) * | 2016-06-22 | 2017-12-28 | 石原ケミカル株式会社 | Detergent composition for car air conditioner and aerosol composition using the same |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102009029200A1 (en) * | 2009-09-04 | 2011-03-17 | Wacker Chemie Ag | Isocyanate-free silane-crosslinking compositions |
| JP5583385B2 (en) * | 2009-11-04 | 2014-09-03 | 大日本除蟲菊株式会社 | disinfectant |
| JP5700558B2 (en) * | 2011-11-02 | 2015-04-15 | ライオン株式会社 | Sheet cosmetic |
| JP6510177B2 (en) * | 2014-04-01 | 2019-05-08 | ロレアル | Compositions in the form of nano or microemulsions |
| WO2015159942A1 (en) * | 2014-04-17 | 2015-10-22 | 株式会社シード | Medical device including anionic drug |
| JP6537788B2 (en) | 2014-06-25 | 2019-07-03 | ロレアル | Composition in the form of a nanoemulsion or microemulsion or having a lamellar structure |
| CN104974859B (en) * | 2015-06-29 | 2017-12-22 | 陈士友 | Waterless carwash liquid |
| KR102638891B1 (en) * | 2017-12-28 | 2024-02-23 | 라이온 가부시키가이샤 | Non-rinse type liquid sterilizing and cleaning agent composition |
| JP7300139B2 (en) * | 2018-07-18 | 2023-06-29 | 株式会社日本色材工業研究所 | oily cosmetics |
| CN110201603B (en) * | 2019-06-13 | 2021-08-13 | 湖南华腾制药有限公司 | Cationic surfactant and preparation method thereof |
| JP7345886B2 (en) * | 2020-05-25 | 2023-09-19 | 株式会社東洋新薬 | Alcohol-containing composition |
| JP7516327B2 (en) * | 2021-09-02 | 2024-07-16 | 花王株式会社 | Disinfection products |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPH06279268A (en) * | 1993-01-27 | 1994-10-04 | Takeda Chem Ind Ltd | Disinfecting and sterilizing agent and aerosol composition containing the same |
| JP3093981B2 (en) * | 1996-04-05 | 2000-10-03 | 花王株式会社 | Detergent composition |
| TW427912B (en) * | 1996-12-20 | 2001-04-01 | Kao Corp | Detergent composition |
| TW401307B (en) * | 1996-12-20 | 2000-08-11 | Kao Corp | Detergent composition |
| JPH10330799A (en) * | 1997-06-04 | 1998-12-15 | Lion Corp | Frothy bactericidal detergent composition |
| JP2001139993A (en) * | 1999-11-17 | 2001-05-22 | Fumakilla Ltd | Disinfection detergent for skin |
| JP4025950B2 (en) * | 2000-04-28 | 2007-12-26 | ライオン株式会社 | Bactericidal compound-containing composition |
| JP5041113B2 (en) * | 2001-08-20 | 2012-10-03 | ライオン株式会社 | Liquid detergent composition |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2017226766A (en) * | 2016-06-22 | 2017-12-28 | 石原ケミカル株式会社 | Detergent composition for car air conditioner and aerosol composition using the same |
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| HK1145511A1 (en) | 2011-04-21 |
| JP5343857B2 (en) | 2013-11-13 |
| KR20100106975A (en) | 2010-10-04 |
| KR101443951B1 (en) | 2014-09-23 |
| WO2009075142A1 (en) | 2009-06-18 |
| CN101896595A (en) | 2010-11-24 |
| MY155282A (en) | 2015-09-30 |
| CN101896595B (en) | 2012-04-25 |
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