WO1999029815A1 - Dishwashing detergent with antibacterial action - Google Patents
Dishwashing detergent with antibacterial action Download PDFInfo
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- WO1999029815A1 WO1999029815A1 PCT/EP1998/007698 EP9807698W WO9929815A1 WO 1999029815 A1 WO1999029815 A1 WO 1999029815A1 EP 9807698 W EP9807698 W EP 9807698W WO 9929815 A1 WO9929815 A1 WO 9929815A1
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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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
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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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/94—Mixtures with anionic, cationic or non-ionic compounds
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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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2086—Hydroxy carboxylic acids-salts thereof
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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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
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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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
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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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/662—Carbohydrates or derivatives
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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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/90—Betaines
Definitions
- the invention relates to dishwashing detergents which, when used in concentrated form, show an antibacterial effect, i.e. when used undiluted, inhibit bacterial growth and, in addition, kill a large number of bacteria.
- the object of the invention was to formulate a hand dishwashing detergent that too with a 50% dilution, there is still a significant inhibition of bacterial growth and, to a large extent, also causes germ killing.
- a modern hand dishwashing detergent must also have a special range of properties, which include excellent cleaning, skin compatibility, temperature and storage stability and ecological compatibility.
- Antibacterial detergents are known in the prior art.
- a bacteriostatic component i.a. Triclosan (2,4,4'-trichloro-2'-hydroxydiphenyl ether)
- natural or nature-identical extracts e.g. Extracts from orange peel, pine oil, geraniol, nerol etc. are used.
- the bacteriostatic effect is not sufficient to guarantee sufficient inhibition of bacterial growth when using the hand dishwashing liquid using moist dishcloths, sponges or brushes.
- chloramine-T Toluolsulfonklarechloramid-sodium salt
- Germall ® 115 imidazolidinyl urea
- sodium formate 2-phenoxyethanol, 1-phenoxy-2-propanol, 2-phenoxy-l-propanol showed particularly at 50% Use concentration not sufficient antibacterial effect.
- compositions proposed in the prior art is suitable as an arbitrarily perfumable, excellently cleansing, skin-compatible, temperature- and storage-stable and ecologically particularly compatible hand dishwashing detergent with specific antibacterial activity in concentrated use on moist surfaces. worktops, kitchen appliances using wet dishcloths, sponges and brushes.
- the present invention accordingly relates to an antibacterial hand dishwashing detergent containing surfactant mixtures of anionic surfactants and / or nonionic surfactants and / or betaine surfactants, which contains one or more carboxylic acids and / or their salts with antibacterial activity.
- the present invention also relates to the use of one or more carboxylic acids and / or their salts as antibacterial components in hand dishwashing detergents.
- a particular advantage of the hand dishwashing detergent according to the invention is its good antibacterial activity against the kitchen hygiene-relevant herpes viruses, with which cutlery and glasses can be easily contaminated when used by infectious persons.
- Carboxylic acids or carboxylic acid salts in the context of the present invention are, in particular, benzoic acid (phenyl formic acid), lactic acid (2-hydroxypropionic acid), salicylic acid (2-hydroxybenzoic acid), sorbic acid (2,4-hexadienoic acid) or mixtures thereof and / or their sodium, Potassium, magnesium or calcium salts and mixtures thereof.
- antibacterial active ingredients are benzoic acid and / or its sodium salt, salicylic acid and / or its sodium salt, lactic acid and / or its sodium salt and mixtures of two or more carboxylic acids and / or their salts.
- Benzoic acid is particularly suitable.
- an application concentration between 0.1 and 8% by weight, preferably between 0.5 and 6% by weight and particularly preferably between 1 and 4% by weight.
- the suitable amount of carboxylic acid and / or carboxylic acid salt in the case of a combined use of active ingredient is between 0.05 and 2% by weight, preferably between 0.1 and 1% by weight and particularly preferably between 0.2 and 0.5% by weight. -%.
- the amount of imidazolidinyl urea used in this case is between 0.05 and 2% by weight, preferably between 0.1 and 1.5% by weight and particularly preferably between 0.2 and 1% by weight.
- surfactant mixtures are those made from anionic and nonionic surfactants.
- betaine surfactants in a mixture can also be very useful for many applications.
- the surfactants are used in amounts of 0.4 to 50% by weight, preferably 1 to 45% by weight, particularly preferably 3 to 42% by weight and extremely preferably 5 to 40% by weight.
- Anionic surfactants according to the present invention can be aliphatic sulfates such as fatty alcohol sulfates, fatty alcohol ether sulfates, dialkyl ether sulfates, monoglyceride sulfates and aliphatic sulfonates such as alkane sulfonates, olefin sulfonates, ether sulfonates, n-alkyl ether sulfonates, ester sulfonates, and lingine sulfonates.
- aliphatic sulfates such as fatty alcohol sulfates, fatty alcohol ether sulfates, dialkyl ether sulfates, monoglyceride sulfates and aliphatic sulfonates such as alkane sulfonates, olefin sulfonates, ether sulfonates, n-alkyl ether sulf
- Fatty acid cyanamides, sulfosuccinic esters, fatty acid isethionates, acylaminoalkanesulfonates (fatty acid taurides), fatty acid sarcosinates, ether carboxylic acids and alkyl (ether) phosphates can also be used in the context of the present invention.
- the fatty alcohol ether sulfates are particularly preferred in the context of the present invention.
- Fatty alcohol ether sulfates are products of sulfation reactions on alkoxylated alcohols. The person skilled in the art generally understands by alkoxylated alcohols the reaction products of alkylene oxide, preferably ethylene oxide, with alcohols, preferably the longer-chain alcohols in the sense of the present invention.
- n moles of ethylene oxide and one mole of alcohol form a complex mixture of addition products of different degrees of ethoxylation, depending on the reaction conditions.
- Another embodiment is the use of mixtures of the alkylene oxides, preferably the mixture of ethylene oxide and propylene oxide.
- Low-ethoxylated fatty alcohols 0.5-4 mol EO, preferably 1-2 mol EO are very particularly preferred for the purposes of the present invention.
- the anionic surfactants are preferably used in amounts between 0.2 and 39.8% by weight, preferably 5 to 35% by weight, particularly preferably 10 to 32% by weight. However, amounts up to about 45% by weight can also be used, e.g. B. if the use of fatty alcohol sulfates is intended.
- Nonionic surfactants in the context of the present invention can be alkoxyates such as polyglycol ethers, fatty alcohol polyglycol ethers, alkylphenol polyglycol ethers, end-capped polyglycol ethers, mixed ethers and hydroxy mixed ethers and fatty acid polyglycol esters. Ethylene oxide, propylene oxide, block polymers and fatty acid alkanolamides and fatty acid polyglycol ethers can also be used.
- An important class of nonionic surfactants that can be used according to the invention are the polyol surfactants and here in particular the glucosurfactants, such as alkyl polyglycosides and fatty acid glucamides. The alkyl polyglucosides are particularly preferred.
- Alkyl polyglycosides are surfactants which can be obtained by the reaction of sugars and alcohols according to the relevant methods of preparative organic chemistry. Depending on the type of preparation, a mixture of monoalky cheerful, oligomeric or polymeric sugars results.
- Preferred alkyl polyglycosides can be alkyl polyglucosides, the alcohol being a long-chain fatty alcohol or a mixture of long-chain fatty alcohols with branched or unbranched alkyl chain lengths between Cg and C 18 and the degree of oligomerization of the sugars being between 1 and 10 being particularly preferred.
- the alkyl polyglycosides are particularly preferably used in amounts between 0.1 to 14.9% by weight, preferably 0.5 to 8% by weight and particularly preferably 1 to 6% by weight.
- the zwitterionic surfactants or amphoteric surfactants which can be used according to the invention include the alkyl betaines, the alkyl amido betaines, the imidazolinium betaines and the aminopropionates, as well as the sulfobetaines and biosurfactants.
- a preferred ingredient is alkyl amido betaine.
- amphoteric surfactants are preferably used in amounts between 0.1 to 14.9% by weight, preferably 0.5 to 8% by weight and particularly preferably 1 to 6% by weight.
- the hand dishwashing detergent contains as surfactant mixture (a) 0.2 to 39.8% by weight, preferably 5 to 35% by weight, particularly preferably 10 to 32% by weight, anionic surfactants, preferably fatty alcohol ether sulfates and / or fatty alcohol sulfates, (b) 0.1 to 14.9% by weight, preferably 0.5 to 8% by weight and particularly preferably 1 to 6% by weight, nonionic surfactants, preferably alkyl polyglucosides, and (c) 0.1 to 14.9% by weight, preferably 0.5 to 8% by weight and particularly preferably 1 to 6% by weight, betaine surfactants, preferably alkylamido betaines.
- anionic surfactants preferably fatty alcohol ether sulfates and / or fatty alcohol sulfates
- nonionic surfactants preferably alkyl polyglucosides
- betaine surfactants preferably alkylamido betaines.
- solubilizers for example for dyes and perfume oils, for example alkanolamines, polyols such as ethylene glycol, propylene glycol, 1,2 glycerol and other mono- and polyhydric alcohols, and also alkylbenzenesulfonates with 1 to 3 carbon atoms in the alkyl radical can be used.
- alkanolamines polyols such as ethylene glycol, propylene glycol, 1,2 glycerol and other mono- and polyhydric alcohols
- alkylbenzenesulfonates with 1 to 3 carbon atoms in the alkyl radical
- solvents for example one or more low molecular weight alcohols, for example ethanol. They contribute to the incorporation of perfume and dye, prevent the formation of liquid-crystalline phases and play a part in the formation of clear products. According to the invention, between 0 and 12% by weight, preferably between 3 and 10% by weight, particularly preferably between 5 and 8% by weight, of solvents can be present.
- ingredients that are customary in hand dishwashing detergents, such as defoamers (such as silicone oils, paraffin oils or mineral oils), structuring agents, perfume substances, dyes, corrosion inhibitors, preservatives or the like, common ingredients in hand dishwashing detergents in amounts of up to 5% by weight. be included.
- defoamers such as silicone oils, paraffin oils or mineral oils
- structuring agents such as silicone oils, paraffin oils or mineral oils
- perfume substances such as silicone oils, paraffin oils or mineral oils
- dyes such as dyes, corrosion inhibitors, preservatives or the like
- the antibacterial effect of the hand dishwashing detergent according to the invention is exemplified by the following recipes (in the tables of Examples 1 and 2, the unit% stands for% by weight).
- the specified pH values were adjusted with citric acid.
- Test method quantitative suspension test based on the DGHM test methodology
- Test germ Salmonelle Enteritidis (practice isolate)
- Test concentration 50% in DGHM water (17 ° dH) Test temperature: room temperature Exposure time: 15 minutes Example 2
- formulations 8 and 9 which are completely effective against herpes viruses, on the basis of the following basic formulation.
- both formulations contained small amounts of color and fragrance.
- a pH of 5.2 was set in each case with citric acid.
- Active ingredient 2.35% sodium benzoate 1.75% sodium benzoate + 1.50% lactic acid logarithmic reduction factor herpes virus
- test methodology was based on the guidelines of the Federal Health Office (BGA) and the German Association for Combating Virus Diseases (DVV) for testing chemical disinfectants for their effectiveness against viruses in the version dated September 1, 1982 ⁇ Bundes Canal 1982, 25, No. 12, 397- 398) with the following deviations that 1.) instead of the test viruses prescribed there herpes simplex-Vi ⁇ us, strain HV342 (cultivation on the Nero cells specified in the guideline) was used, 2.) instead of the room temperature specified there the test temperatures given above of 30 and 40 ° C and
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Abstract
Description
.Geschirrspülmittel mit antibakterieller Wirkung" "Dishwashing liquid with antibacterial effect"
Die Erfindung betrifft Geschirrspülmittel, die bei konzentrierter Anwendung eine antibakterielle Wirkung zeigen, d.h. bei unverdünnter Anwendung eine Hemmung des bakteriellen Wachstums bewirken und darüber hinaus eine Reihe von Bakterien in erheblichem Umfange abtöten.The invention relates to dishwashing detergents which, when used in concentrated form, show an antibacterial effect, i.e. when used undiluted, inhibit bacterial growth and, in addition, kill a large number of bacteria.
Eine der meist unterschätzten Gesundheitsgefahren sind die hygienischen Verhältnisse in der Küche. Krankheitserregende Bakterien können sich - insbesondere nach Verarbeitung von Eiern, rohem Fleisch und rohem Fisch - auf Arbeitsflächen und Küchengeräten, wie z.B. Schneidbrettern vermehren und damit eine ernste Gefahr darstellen.One of the most underestimated health risks is the hygienic conditions in the kitchen. Disease-causing bacteria - especially after processing eggs, raw meat and raw fish - can spread on work surfaces and kitchen appliances, e.g. Increase cutting boards and pose a serious danger.
Versucht man mit herkömmlichen Geschirrspülmitteln eine bakteriostatische Wirkung zu erreichen, so stellt man bei der Überprüfung der antibakteriellen Wirksamkeit schnell fest, daß eine Reihe von Handgeschirrspülmittel schon bei konzentrierter Anwendung keine ausreichende Wachstumshemmung oder gar Keimabtötung bewirken.If one tries to achieve a bacteriostatic effect with conventional dishwashing detergents, it is quickly found when checking the antibacterial effectiveness that a number of hand dishwashing detergents do not sufficiently inhibit growth or even kill germs even with concentrated use.
Die Anwendung von konzentriertem Produkt auf feuchten Arbeitsflächen oder Küchengeräten unter Zuhilfenahme von feuchten Spülschwämmen, Tüchern oder Bürsten führt zudem zwangsläufig zu einer Verdünnung des Handgeschirrspülmittels und damit zu einer weiter reduzierten antibakteriellen Wirkung.The use of concentrated product on damp work surfaces or kitchen appliances with the help of damp sponges, cloths or brushes also leads inevitably to a dilution of the hand dishwashing liquid and thus to a further reduced antibacterial effect.
Eine Überprüfung der antibakteriellen Wirkung von Handgeschirrspülmittelformulierungen nach dem in der Desinfektionsmittelprüfung anerkannten „quantitativen Suspensionstest" der DGHM (Deutsche Gesellschaft für Hygiene und Mikrobiologie), bei dem die Zahl überlebender Keime nach Ablauf einer definierten, praxisrelevanten Einwirkzeit in Abhängigkeit von der Einsatzkonzentration bestimmt wird, hat nun gezeigt, daß schon bei Einsatz einer 50 %igen Spülmittelverdünnung eine Reihe von Konservierungsmittel- haltigen Rezepturen keine ausreichende bakteriostatische Wirkung aufweisen.A review of the antibacterial effect of hand dishwashing agent formulations according to the "quantitative suspension test" of the DGHM (German Society for Hygiene and Microbiology) recognized in the disinfectant test, in which the number of surviving germs is determined after a defined, practice-relevant exposure time depending on the concentration in use now shown that even when using a 50% detergent dilution, a number of formulations containing preservatives do not have a sufficient bacteriostatic effect.
Aufgabe der Erfindung war es nun, ein Handgeschirrspülmittel zu formulieren, daß auch bei 50 %iger Verdünnung noch eine deutliche Hemmung des Bakterienwachstums und zudem in hohem Maße eine Keimabtötung bewirkt.The object of the invention was to formulate a hand dishwashing detergent that too with a 50% dilution, there is still a significant inhibition of bacterial growth and, to a large extent, also causes germ killing.
Daneben muß ein modernes Handgeschirrspülmittel auch ein besonderes Eigenschaftsspektrum aufweisen, welches ausgezeichnete Reinigungung, Hautverträglichkeit, Temperatur- und Lagerstabilität und ökologische Verträglichkeit umfaßt.In addition, a modern hand dishwashing detergent must also have a special range of properties, which include excellent cleaning, skin compatibility, temperature and storage stability and ecological compatibility.
Antibakterielle Spülmittel sind im Stand der Technik bekannt. Als bakteriostatische Komponente werden u.a. Triclosan (2,4,4'-Trichlor-2'-hydroxydiphenylether), natürliche bzw. natur-identische Extrakte, wie z.B. Extrakte aus der Orangenschale, Pineöl, Geraniol, Nerol usw. verwendet.Antibacterial detergents are known in the prior art. As a bacteriostatic component, i.a. Triclosan (2,4,4'-trichloro-2'-hydroxydiphenyl ether), natural or nature-identical extracts, e.g. Extracts from orange peel, pine oil, geraniol, nerol etc. are used.
Ein Einsatz ökologisch und ökonomisch vertretbarer Triclosan-Mengen fuhrt zwar zu einer ausreichenden antibakteriellen Wirkung bei 100 %iger Anwendungskonzentration, bei Prüfung der antibakteriellen Eigenschaften bei einer Einsatzkonzentration von 50 % ist aber keine ausreichende Hemmwirkung auf das Bakterienwachstum mehr gegeben.The use of ecologically and economically justifiable amounts of triclosan leads to a sufficient antibacterial effect at 100% application concentration, but when the antibacterial properties are tested at an application concentration of 50% there is no longer sufficient inhibitory effect on bacterial growth.
Arbeitet man relativ hohen Mengen natürlicher oder naturidentischer Extrakte ein, so ergeben sich - neben Problemen bei der homogenen Einarbeitung der Wirkstoffe - auch Parfumierungprobleme, da die geruchsintensiven Extrakte nicht oder nur mühsam in die vom Entwickler gewünschte Duftrichtung überparfümiert werden können.If relatively large amounts of natural or nature-identical extracts are worked in, then - in addition to problems with the homogeneous incorporation of the active ingredients - there are also problems with perfuming, since the odor-intensive extracts cannot be perfumed, or only with difficulty, in the fragrance direction desired by the developer.
Bei niedrigen Einsatzmengen reicht die bakteriostatische Wirkung nicht aus, um auch eine ausreichende Hemmung des Bakterienwachstums bei Anwendung des Handgeschirrspülmittels unter Nutzung feuchter Spültücher, Schwämme oder Bürsten zu garantieren.When used in small quantities, the bacteriostatic effect is not sufficient to guarantee sufficient inhibition of bacterial growth when using the hand dishwashing liquid using moist dishcloths, sponges or brushes.
Andere Wirkstoffe, wie z.B. Chloramin-T (Toluolsulfonsäurechloramid-Natriumsalz), Germall® 115 (Imidazolidinyl-Harnstoff), Natriumformiat, 2-Phenoxyethanol, 1- Phenoxy-2-propanol, 2-Phenoxy-l-propanol zeigten insbesondere bei 50 %iger Einsatzkonzentration keine ausreichende antibakterielle Wirkung.Other active ingredients, such as chloramine-T (Toluolsulfonsäurechloramid-sodium salt), Germall ® 115 (imidazolidinyl urea), sodium formate, 2-phenoxyethanol, 1-phenoxy-2-propanol, 2-phenoxy-l-propanol showed particularly at 50% Use concentration not sufficient antibacterial effect.
Keine im Stand der Technik vorgeschlagenen Zusammensetzungen eignet sich demnach als beliebig parfümierbares, ausgezeichnet reinigendes, hautverträgliches, temperatur- und lagerstabiles und ökologisch besonders verträgliches Handgeschirrspülmittel mit spezifischer -antibakterieller Wirksamkeit bei konzentrierter Anwendung auf feuchten Ar- beitsflächen, Küchengeräten unter Nutzung feuchter Spültücher, Schwämme und Bürsten.Accordingly, none of the compositions proposed in the prior art is suitable as an arbitrarily perfumable, excellently cleansing, skin-compatible, temperature- and storage-stable and ecologically particularly compatible hand dishwashing detergent with specific antibacterial activity in concentrated use on moist surfaces. worktops, kitchen appliances using wet dishcloths, sponges and brushes.
Problemlos parfümierbare, ausgezeichnet reinigende, hautverträgliche, temperatur- und lagerstabile und ökologisch besonders verträgliche Produkte mit guter antibakterieller Wirksamkeit bei konzentrierter Anwendung erhält man, wenn man ein Gemisch aus Fet- talkoholethersulfat, ggf. Fettalkoholsulfat, Alkylpolyglykosid und Betain zusammen mit einer Carbonsäure bzw. deren Salze bereitstellt.Easily perfumed, excellent cleaning, skin-compatible, temperature- and storage-stable and ecologically particularly compatible products with good antibacterial activity with concentrated use are obtained by mixing a mixture of fatty alcohol sulfate, possibly fatty alcohol sulfate, alkyl polyglycoside and betaine together with a carboxylic acid or their Provides salts.
Gegenstand vorliegender Erfindung ist demnach ein antibakterielles Handgeschirrspülmittel, enthaltend Tensidmischungen aus anionischen Tensiden und/oder nichtionischen Tensiden und/oder Betaintenside, das eine oder mehrere Carbonsäuren und/oder deren Salze mit antibakterieller Wirkung enthält.The present invention accordingly relates to an antibacterial hand dishwashing detergent containing surfactant mixtures of anionic surfactants and / or nonionic surfactants and / or betaine surfactants, which contains one or more carboxylic acids and / or their salts with antibacterial activity.
Ebenfalls Gegenstand vorliegender Erfindung ist die Verwendung von einer oder mehreren Carbonsäuren und/oder deren Salzen als antibakterielle Komponente in Handgeschirrspülmitteln.The present invention also relates to the use of one or more carboxylic acids and / or their salts as antibacterial components in hand dishwashing detergents.
Ein besonderer Vorteil des erfindungsgemäßen Handgeschirrspülmittels ist seine gute antibakterielle Wirksamkeit gegen die küchenhygienisch relevanten Herpes-Viren, mit denen Besteckteile und Gläser bei der Benutzung durch infektiöse Personen leicht kontaminiert werden können.A particular advantage of the hand dishwashing detergent according to the invention is its good antibacterial activity against the kitchen hygiene-relevant herpes viruses, with which cutlery and glasses can be easily contaminated when used by infectious persons.
Carbonsäuren bzw. Carbonsäuresalze im Sinne der vorliegenden Erfindung sind besonders Benzoesäure (Phenylameisensäure), Milchsäure (2-Hydroxypropionsäure), Salicyl- säure (2-Hydroxybenzoesäure), Sorbinsäure (2,4-Hexadiensäure) oder deren Mischungen und/oder deren Natrium-, Kalium-, Magnesium- oder Calciumsalze sowie deren Mischungen.Carboxylic acids or carboxylic acid salts in the context of the present invention are, in particular, benzoic acid (phenyl formic acid), lactic acid (2-hydroxypropionic acid), salicylic acid (2-hydroxybenzoic acid), sorbic acid (2,4-hexadienoic acid) or mixtures thereof and / or their sodium, Potassium, magnesium or calcium salts and mixtures thereof.
Es wurde überaschend gefunden, daß besonders geeignete antibakterielle Wirkstoffe Benzoesäure und/oder deren Natriumsalz, Salicylsäure und/oder deren Natriumsalz, Milchsäure und/oder deren Natriumsalz sowie Mischungen von zwei oder mehreren Carbonsäuren und/oder deren Salze sind. Insbesondere geeignet ist die Benzoesäure.It has surprisingly been found that particularly suitable antibacterial active ingredients are benzoic acid and / or its sodium salt, salicylic acid and / or its sodium salt, lactic acid and / or its sodium salt and mixtures of two or more carboxylic acids and / or their salts. Benzoic acid is particularly suitable.
Zur Sicherstellung einer ausreichenden Hemmung des Bakterienwachstums sowie zu einer möglichst hohen Keimabtötungsrate ist eine Einsatzkonzentration zwischen 0,1 und 8 Gew.-%, bevorzugt zwischen 0,5 und 6 Gew.-% und besonders bevorzugt zwischen 1 und 4 Gew.-%, anzustreben.To ensure sufficient inhibition of bacterial growth and the highest possible rate of germ killing, an application concentration between 0.1 and 8% by weight, preferably between 0.5 and 6% by weight and particularly preferably between 1 and 4% by weight.
Überraschenderweise wurde zudem gefunden, daß es eine kombinierte Verwendung von Carbonsäuren und/oder Carbonsäuresalzen zusammen mit Imidazolinidyl-Harnstoff, z.B. Germall® 115, ermöglicht, - unter Beibehaltung der guten bakteriostatischen Eigenschaften - die Einsatzmenge an Carbonsäure und/oder Carbonsäuresalz drastisch zu senken. Die geeignete Einsatzmenge an Carbonsäure und/oder Carbonsäuresalz liegt im Falle eines kombinierten Wirkstoffeinsatzes zwischen 0,05 und 2 Gew.-%, bevorzugt zwischen 0,1 und 1 Gew.-% und besonders bevorzugt zwischen 0,2 und 0,5 Gew.-%. Die Einsatzmenge an Imidazolidinyl-Harnstoff liegt in diesem Fall zwischen 0,05 und 2 Gew.-%, bevorzugt zwischen 0,1 und l,5 Gew.-% und besonders bevorzugt zwischen 0,2 und 1 Gew.-%.Surprisingly, it was also found that 115 enables the combined use of carboxylic acids and / or carboxylic acid salts with imidazolinidyl urea, for example Germall® ®, - while retaining the good bacteriostatic properties - the use amount of carboxylic acid and / or lower carboxylic acid salt dramatically. The suitable amount of carboxylic acid and / or carboxylic acid salt in the case of a combined use of active ingredient is between 0.05 and 2% by weight, preferably between 0.1 and 1% by weight and particularly preferably between 0.2 and 0.5% by weight. -%. The amount of imidazolidinyl urea used in this case is between 0.05 and 2% by weight, preferably between 0.1 and 1.5% by weight and particularly preferably between 0.2 and 1% by weight.
Es wurde außerdem gefunden, daß - im Sinne der Erfindung - eine Carbonsäure- und/oder Carbonsäuresalz-haltige Spülmittelformulierung bei einem pH- Wert im Fertigprodukt zwischen 4 und 6, bevorzugt zwischen 4,5 und 5,5, besonders bevorzugt zwischen 4,9 und 5,3, die stärkste antibakterielle Wirksamkeit gepaart mit der günstigsten Lagerstabilität aufweist.It has also been found that - for the purposes of the invention - a detergent formulation containing carboxylic acid and / or carboxylic acid salt at a pH in the finished product between 4 and 6, preferably between 4.5 and 5.5, particularly preferably between 4.9 and 5.3, which has the strongest antibacterial activity paired with the most favorable storage stability.
Als Tensidmischungen eignen sich besonders jene aus anionischen und nichtionischen Tensiden. Aber auch die zusätzliche Verwendung von Betaintensiden im Gemisch kann für viele Anwendungen sehr sinnvoll sein. Insgesamt verwendet man die Tenside in Mengen von 0,4 bis 50 Gew.-, bevorzugt von 1 bis 45 Gew.-%, besonders bevorzugt 3 bis 42 Gew.- und äußerst bevorzugt 5 bis 40 Gew.-%.Particularly suitable surfactant mixtures are those made from anionic and nonionic surfactants. However, the additional use of betaine surfactants in a mixture can also be very useful for many applications. In total, the surfactants are used in amounts of 0.4 to 50% by weight, preferably 1 to 45% by weight, particularly preferably 3 to 42% by weight and extremely preferably 5 to 40% by weight.
Anionische Tenside gemäß der vorliegenden Erfindung können aliphatische Sulfate wie Fettalkoholsulfate, Fettalkoholethersulfate, Dialkylethersulfate, Monoglyceridsulfate und aliphatische Sulfonate wie Alkansulfonate, Olefmsulfonate, Ethersulfonate, n-Alkylether- sulfonate, Estersulfonate, und Lingninsulfonate sein. Ebenfalls im Rahmen der vorliegenden Erfindung verwendbar sind Fettsäurecyanamide, Sulfobernsteinsäureester, Fettsäure- isethionate, Acylaminoalkansulfo-nate (Fettsäuretauride), Fettsäuresarcosinate, Ethercar- bonsäuren und Alkyl(ether)phosphate. Besonders bevorzugt im Rahmen der vorliegenden Erfindung sind die Fettalkoholethersulfate. Fettalkoholethersulfate sind Produkte von Sulfatierreaktionen an alkoxylierten Alkoholen. Dabei versteht der Fachmann allgemein unter alkoxylierten Alkoholen die Reaktionsprodukte von Alkylenoxid, bevorzugt Ethylenoxid, mit Alkoholen, bevorzugt im Sinne der vorliegenden Erfindung die längerkettigen Alkohole. In der Regel enstehen aus n Molen Ethylenoxid und einem Mol Alkohol, abhängig von den Reaktionsbedingungen ein komplexes Gemisch von Additionsprodukten unterschiedlichen Ethoxylierungs- grades. Eine weitere Ausfuhrungsform besteht im Einsatz von Gemischen der Alkylen- oxide bevozugt des Gemisches von Ethylenoxid und Propylenoxid. Ganz besonders bevorzugt im Sinne der vorliegenden Erfindung sind niederethoxylierte Fettalkohole (0,5 - 4 mol EO, bevorzugt 1 - 2 mol EO).Anionic surfactants according to the present invention can be aliphatic sulfates such as fatty alcohol sulfates, fatty alcohol ether sulfates, dialkyl ether sulfates, monoglyceride sulfates and aliphatic sulfonates such as alkane sulfonates, olefin sulfonates, ether sulfonates, n-alkyl ether sulfonates, ester sulfonates, and lingine sulfonates. Fatty acid cyanamides, sulfosuccinic esters, fatty acid isethionates, acylaminoalkanesulfonates (fatty acid taurides), fatty acid sarcosinates, ether carboxylic acids and alkyl (ether) phosphates can also be used in the context of the present invention. The fatty alcohol ether sulfates are particularly preferred in the context of the present invention. Fatty alcohol ether sulfates are products of sulfation reactions on alkoxylated alcohols. The person skilled in the art generally understands by alkoxylated alcohols the reaction products of alkylene oxide, preferably ethylene oxide, with alcohols, preferably the longer-chain alcohols in the sense of the present invention. As a rule, n moles of ethylene oxide and one mole of alcohol form a complex mixture of addition products of different degrees of ethoxylation, depending on the reaction conditions. Another embodiment is the use of mixtures of the alkylene oxides, preferably the mixture of ethylene oxide and propylene oxide. Low-ethoxylated fatty alcohols (0.5-4 mol EO, preferably 1-2 mol EO) are very particularly preferred for the purposes of the present invention.
Bevorzugt werden die anionischen Tenside in Mengen zwischen 0,2 und 39,8 Gew.-% eingesetzt, bevorzugt 5 bis 35 Gew.-%, besonders bevorzugt 10 bis 32 Gew.-%. Aber auch Mengen bis ungefähr 45 Gew.-% können verwendet werden, z. B. wenn die Verwendung von Fettalkoholsulfaten beabsichtigt wird.The anionic surfactants are preferably used in amounts between 0.2 and 39.8% by weight, preferably 5 to 35% by weight, particularly preferably 10 to 32% by weight. However, amounts up to about 45% by weight can also be used, e.g. B. if the use of fatty alcohol sulfates is intended.
Nichtionische Tenside im Rahmen der vorliegenden Erfindung können Alkoxyiate sein wie Polyglycolether, Fettalkoholpolygycolether, Alkylphenolpolyglycolether, endgrup- penver-schlossene Polyglycolether, Mischether und Hydroxymischether und Fettsäure- polyglycolester sein. Ebenfalls verwendbar sind Ethylenoxid, Propylenoxid, Blockpolymere und Fettsäurealkanolamide und Fettsäurepolyglycolether. Eine wichtige Klasse nichtionischer Tenside die erfindungsgemäß verwendet werden kann, sind die Polyol- Tenside und hier besonders die Glucotenside, wie Alkylpolyglycoside und Fettsäu- reglucamide. Besonders bevorzugt sind die Alkylpolyglucoside.Nonionic surfactants in the context of the present invention can be alkoxyates such as polyglycol ethers, fatty alcohol polyglycol ethers, alkylphenol polyglycol ethers, end-capped polyglycol ethers, mixed ethers and hydroxy mixed ethers and fatty acid polyglycol esters. Ethylene oxide, propylene oxide, block polymers and fatty acid alkanolamides and fatty acid polyglycol ethers can also be used. An important class of nonionic surfactants that can be used according to the invention are the polyol surfactants and here in particular the glucosurfactants, such as alkyl polyglycosides and fatty acid glucamides. The alkyl polyglucosides are particularly preferred.
Alkylpolyglycoside sind Tenside, die durch die Reaktion von Zuckern und Alkoholen nach den einschlägigen Verfahren der präparativen organischen Chemie erhalten werden können, wobei es je nach Art der Herstellung zu einem Gemisch monoalky Heiter, oligo- merer oder polymerer Zucker kommt. Bevorzugte Alkylpolyglykoside können Alkylpolyglucoside sein, wobei besonders bevorzugt der Alkohol ein langkettiger Fettalkohol ist oder ein Gemisch langkettiger Fett-alkohole ist mit verzweigten oder unverzweigten Al- kylkettenlängen zwischen Cg und C18 und der Oligomerisierungsgrad der Zucker zwischen 1 und 10 ist. Besonders bevorzugt verwendet man die Alkylpolyglycoside in Mengen zwischen 0,1 bis 14,9 Gew.-%, bevorzugt 0,5 bis 8 Gew.-% und besonders bevorzugt 1 bis 6 Gew.-%.Alkyl polyglycosides are surfactants which can be obtained by the reaction of sugars and alcohols according to the relevant methods of preparative organic chemistry. Depending on the type of preparation, a mixture of monoalky cheerful, oligomeric or polymeric sugars results. Preferred alkyl polyglycosides can be alkyl polyglucosides, the alcohol being a long-chain fatty alcohol or a mixture of long-chain fatty alcohols with branched or unbranched alkyl chain lengths between Cg and C 18 and the degree of oligomerization of the sugars being between 1 and 10 being particularly preferred. The alkyl polyglycosides are particularly preferably used in amounts between 0.1 to 14.9% by weight, preferably 0.5 to 8% by weight and particularly preferably 1 to 6% by weight.
Zu den zwitterionischen Tensiden oder Amphotensiden, die erfindungsgemäß eingesetzt werden können, zählen die Alkylbetaine, die Alkylamidobetaine, die Imidazoliniumbetai- ne und die Aminopropionate, genauso wie die Sulfobetaine und Biotenside. Ein bevorzugter Inhaltsstoff ist Alkylamidobetain.The zwitterionic surfactants or amphoteric surfactants which can be used according to the invention include the alkyl betaines, the alkyl amido betaines, the imidazolinium betaines and the aminopropionates, as well as the sulfobetaines and biosurfactants. A preferred ingredient is alkyl amido betaine.
Bevorzugt werden diese Amphotenside in Mengen zwischen 0,1 bis 14,9 Gew.-%, bevorzugt 0,5 bis 8 Gew.-% und besonders bevorzugt 1 bis 6 Gew.-%, eingesetzt.These amphoteric surfactants are preferably used in amounts between 0.1 to 14.9% by weight, preferably 0.5 to 8% by weight and particularly preferably 1 to 6% by weight.
In einer bevorzugten Ausfuhrungsform der Erfindung enthält das Handgeschirrspülmittel als Tensidmischung (a) 0,2 bis 39,8 Gew.-%, bevorzugt 5 bis 35 Gew.-%, besonders bevorzugt 10 bis 32 Gew.-%, anionische Tenside, vorzugsweise Fettalkoholethersulfate und/oder Fettalkoholsulfate, (b) 0,1 bis 14,9 Gew.-%, bevorzugt 0,5 bis 8 Gew.-% und besonders bevorzugt 1 bis 6 Gew.-%, nichtionische Tenside, vorzugsweise Alkylpolyglu- coside, und (c) 0,1 bis 14,9 Gew.-%, bevorzugt 0,5 bis 8 Gew.-% und besonders bevorzugt 1 bis 6 Gew.-%, Betaintenside, vorzugsweise Alkylamidobetaine.In a preferred embodiment of the invention, the hand dishwashing detergent contains as surfactant mixture (a) 0.2 to 39.8% by weight, preferably 5 to 35% by weight, particularly preferably 10 to 32% by weight, anionic surfactants, preferably fatty alcohol ether sulfates and / or fatty alcohol sulfates, (b) 0.1 to 14.9% by weight, preferably 0.5 to 8% by weight and particularly preferably 1 to 6% by weight, nonionic surfactants, preferably alkyl polyglucosides, and (c) 0.1 to 14.9% by weight, preferably 0.5 to 8% by weight and particularly preferably 1 to 6% by weight, betaine surfactants, preferably alkylamido betaines.
Als Lösungsvermittler, etwa für Farbstoffe und Parfumöle können beispielsweise Alka- nolamine, Polyole wie Ethylenglycol, Propylenglycol, 1,2 Glycerin und andere ein- und mehrwertige Alkohole, sowie Alkylbenzolsulfonate mit 1 bis 3 Kohlenstoffatomen im Alkylrest dienen.As solubilizers, for example for dyes and perfume oils, for example alkanolamines, polyols such as ethylene glycol, propylene glycol, 1,2 glycerol and other mono- and polyhydric alcohols, and also alkylbenzenesulfonates with 1 to 3 carbon atoms in the alkyl radical can be used.
Wichtig ist u.a.die Klarheit der Produkte, ein Absetzen von Phasen oder Inhaltsstoffen sowie ein trübes Aussehen ist in der Regel nicht erwünscht.It is important, among other things, that the clarity of the products, the discontinuation of phases or ingredients, and a cloudy appearance is generally not desirable.
Besondere Vorteile erhält man - insbesondere bei hoch tensidhaltigen Mischungen -, wenn man der Formulierung eine Zusammensetzung aus Na-Salzen der Adipin- Bernstein- und Glutarsäure beimengt, wie sie z. B. unter dem Handeslnamen Sokalan® DSC erhältlich ist. Als besonders günstig hat sich hierbei der Einsatz von 0,1 bis 8 Gew.-%, bevorzugt 1 bis 6 Gew.-%, besonders bevorzugt 2,5 bis 5 Gew.-%.Particular advantages are obtained - especially in the case of mixtures containing high surfactants - if the formulation is admixed with a composition of sodium salts of adipic succinic and glutaric acid, as described, for. B. is available under the trade name Sokalan ® DSC. The use of 0.1 to 8% by weight, preferably 1 to 6% by weight, particularly preferably 2.5 to 5% by weight, has proven to be particularly advantageous.
Eine weitere günstige Komponente der erfindungsgemäßen Mittel sind Lösungsmittel Lösungsmittel, beispielsweise ein oder mehrere niedermolekulare Alkohole, z.B. Ethanol. Sie tragen zur Einarbeitung von Parfüm und Farbstoff bei, verhindern die Ausbildung flüssigkristalliner Phasen und haben Anteil an der Bildung klarer Produkte. Erfindungsgemäß können zwischen 0 und 12 Gew.-%, bevorzugt zwischen 3 und 10 Gew.-%, besonders bevorzugt zwischen 5 und 8 Gew.-%, Lösungsmittel enthalten sein.Another cheap component of the agents according to the invention are solvents, solvents, for example one or more low molecular weight alcohols, for example ethanol. They contribute to the incorporation of perfume and dye, prevent the formation of liquid-crystalline phases and play a part in the formation of clear products. According to the invention, between 0 and 12% by weight, preferably between 3 and 10% by weight, particularly preferably between 5 and 8% by weight, of solvents can be present.
Neben den bisher erwähnten Inhaltsstoffen können noch weitere, in Handgeschirrspülmitteln übliche, Inhaltstoffe, wie z.B. Entschäumer (wie z.B. Siliconöle, Paraffinöle oder Mineralöle), Strukturierungsmittel, Parfumstoffe, Farbstoffe Korrosionsinhibitoren, Konservierungsmitteln o.a. in Handgeschirrspülmitteln übliche Inhaltstoffe in Mengen bis zu 5 Gew.-% enthalten sein. In addition to the previously mentioned ingredients, other ingredients that are customary in hand dishwashing detergents, such as defoamers (such as silicone oils, paraffin oils or mineral oils), structuring agents, perfume substances, dyes, corrosion inhibitors, preservatives or the like, common ingredients in hand dishwashing detergents in amounts of up to 5% by weight. be included.
BeispieleExamples
Beispiel 1example 1
Die antibakterielle Wirkung des erfindungsgemäßen Handgeschirrspülmittels sei beispielhaft an folgenden Rezepturen verdeutlicht (in den Tabellen der Beispiele 1 und 2 steht die Einheit % für Gew.-%). Die angegebenen pH- Werte wurden mit Citronensäure eingestellt.The antibacterial effect of the hand dishwashing detergent according to the invention is exemplified by the following recipes (in the tables of Examples 1 and 2, the unit% stands for% by weight). The specified pH values were adjusted with citric acid.
Grundrezeptur: 31,5 Gew.-% C12.ι4 -Fettalkoholethersulfat (1,3 EO) 3,0 Gew.-% C8.i6-Alkylpolyglucosid dpl,4 5,0 Gew.-% Cocoamidopropylbetain 3,5 Gew.-% Dicarbonsäuregemisch (Sokalan®-DSC-Na) x Gew.-% Ethanol y Gew.-% Wirkstoff ad 100,0 Gew.-% WasserBasic formulation: 31.5% by weight of C 12 .ι 4 fatty alcohol ether sulfate (1.3 EO) 3.0% by weight of C 8 .i6-alkyl polyglucoside d p l, 4 5.0% by weight of cocoamidopropylbetaine 3, 5 wt .-% of dicarboxylic acid (Sokalan ® DSC-Na) x wt .-% ethanol y wt .-% of active ingredient 100.0 wt .-% water
Rezeptur 1 2 3 4 5 6 7Recipe 1 2 3 4 5 6 7
Wirkstoff 2,0 % 3,0 % 0,3 % 0,1 % 0,2 % 3,0 % 0,5 % BenzoeMilchGerTriclosan Chloramin Benzyl- Imidazoli- säure säure mall® 115 (Irgasan T (Hala- alkohol nidyl - + DP300) mid) HarnstoffActive ingredient 2.0% 3.0% 0.3% 0.1% 0.2% 3.0% 0.5% BenzoeMilchGerTriclosan Chloramine Benzyl-Imidazolic acid acid mall ® 115 (Irgasan T (Halal alcohol nidyl - + DP300) mid) urea
0,2 % (GerSalicyl- mall® 115) säure0.2% (GerSalicyl-mall ® 115) acid
Ethanol 7,0 % 7,2 % 7,5 % 7,5 % 7,5 % 6,5 % 7,5 % pH-Wert 5,15 5,1 5,2 6,8 7,0 6,8 6,7 logarithm. Reduktionsrate*Ethanol 7.0% 7.2% 7.5% 7.5% 7.5% 6.5% 7.5% pH 5.15 5.1 5.2 6.8 7.0 6.8 6.7 log. Reduction rate *
Salmonella >5,6 4,1 2,7 0,2 - 0,2 0,7 0,07 enteritidisSalmonella> 5.6 4.1 2.7 0.2 - 0.2 0.7 0.07 enteritidis
* Prüfmethode: quantitativer Suspensionstest in Anlehnung an die DGHM-Prüfmethodik Prüfkeim: Salmonelle Enteritidis (Praxisisolat)* Test method: quantitative suspension test based on the DGHM test methodology Test germ: Salmonelle Enteritidis (practice isolate)
Prüfkonzentration: 50 %ig in DGHM-Wasser (17 °dH) Prüftemperatur: Raumtemperatur Einwirkzeit: 15 Minuten Beispiel 2Test concentration: 50% in DGHM water (17 ° dH) Test temperature: room temperature Exposure time: 15 minutes Example 2
Die antibakterielle Wirkung des erfindungsgemäßen Handgeschirrspülmittels sei weiterhin an den vollständig gegen Herpes-Viren wirksamen Rezepturen 8 und 9 auf der Basis der folgenden Grundrezeptur exemplifiziert. Zusätzlich enthielten beide Rezepturen geringe Mengen an Färb- und Duftstoff. Mit Citronensäure wurde jeweils ein pH- Wert von 5,2 eingestellt.The antibacterial effect of the hand dishwashing detergent according to the invention is further exemplified by formulations 8 and 9, which are completely effective against herpes viruses, on the basis of the following basic formulation. In addition, both formulations contained small amounts of color and fragrance. A pH of 5.2 was set in each case with citric acid.
Grundrezeptur: 31,5 Gew.-% C12.14 -Fettalkoholethersulfat (1,3 EO) 5,0 Gew.-% Cs-iö-Alkylpolyglucosid dpl,4 3,0 Gew.-% Cocoamidopropylbetain 3,5 Gew.-% Dicarbonsäuregemisch (Sokalan®-DSC-Na) 6,5 Gew.-% Ethanol y Gew.-% Wirkstoff ad 100,0 Gew.-% WasserBasic formulation: 31.5% by weight of C 12 . 14 -fatty alcohol ether sulfate (1.3 EO) 5.0% by weight Cs-i ö alkyl polyglucoside d p l, 4 3.0% by weight cocoamidopropylbetaine 3.5% by weight dicarboxylic acid mixture (Sokalan ® -DSC-Na ) 6.5 wt .-% ethanol y wt .-% active ingredient ad 100.0 wt .-% water
Rezeptur 8 9Recipe 8 9
Wirkstoff 2,35 % Natrium-Benzoat 1,75 % Natrium-Benzoat + 1,50 % Milchsäure logarithmisch Reduktionsfaktor Herpes-VirusActive ingredient 2.35% sodium benzoate 1.75% sodium benzoate + 1.50% lactic acid logarithmic reduction factor herpes virus
Prüfkonz. 0,04 %ig bei 30 °C >5,5 >5,5Test conc. 0.04% at 30 ° C> 5.5> 5.5
Prüfkonz. 0,20 %ig bei 40 °C nicht bestimmt >5,5Test conc. 0.20% at 40 ° C not determined> 5.5
Die Prüfmethodik basierte auf der Richtlinie des Bundesgesundheitsamtes (BGA) und der Deutschen Vereinigung zur Bekämpfung der Viruskrankheiten (DVV) zur Prüfung von chemischen Desinfektionsmitteln auf Wirksamkeit gegen Viren in der Fassung vom 1.9.1982 {Bundesgesundheitsblatt 1982, 25, Nr. 12, 397-398) mit den folgenden Abweichungen, daß 1.) anstelle der dort vorgeschriebenen Prüfviren Herpes simplex-Viτus, Stamm HV342 (Kultivierung auf den in der Richtlinie angegebenen Nero-Zellen) verwendet wurde, 2.) anstelle der dort angegebenen Raumtemperatur die oben angegebenen Prüftemperaturen von 30 und 40°C zugrunde gelegt wurden undThe test methodology was based on the guidelines of the Federal Health Office (BGA) and the German Association for Combating Virus Diseases (DVV) for testing chemical disinfectants for their effectiveness against viruses in the version dated September 1, 1982 {Bundesgesundheitsblatt 1982, 25, No. 12, 397- 398) with the following deviations that 1.) instead of the test viruses prescribed there herpes simplex-Viτus, strain HV342 (cultivation on the Nero cells specified in the guideline) was used, 2.) instead of the room temperature specified there the test temperatures given above of 30 and 40 ° C and
3.) abweichend von der Richtlinie auf eine zusätzliche Belastung des Testansatzes durch fötales Kälberserum verzichtet wurde. Die Einwirkzeit betrug jeweils 15 Minuten bei den in der Tabelle angegebenen Prüfkonzentrationen. 3.) deviating from the guideline, an additional load on the test approach by fetal calf serum was dispensed with. The exposure time was 15 minutes at the test concentrations shown in the table.
Claims
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98958927A EP1036146B1 (en) | 1997-12-05 | 1998-11-28 | DISHWASHING DETERGENT WITH ANTIBACTERIAL and antiviral ACTION |
| AT98958927T ATE287940T1 (en) | 1997-12-05 | 1998-11-28 | DISHWASHING DETERGENT WITH ANTIBACTERIAL AND ANTIVIRAL EFFECTS |
| JP2000524392A JP2001526301A (en) | 1997-12-05 | 1998-11-28 | Dishwashing detergent with antibacterial action |
| DE59812520T DE59812520D1 (en) | 1997-12-05 | 1998-11-28 | DISHWASHER WITH ANTIBACTERIAL AND ANTIVIRAL EFFECT |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19753982.3 | 1997-12-05 | ||
| DE19753982A DE19753982A1 (en) | 1997-12-05 | 1997-12-05 | Dishwashing liquid with an antibacterial effect |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1999029815A1 true WO1999029815A1 (en) | 1999-06-17 |
Family
ID=7850847
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP1998/007698 Ceased WO1999029815A1 (en) | 1997-12-05 | 1998-11-28 | Dishwashing detergent with antibacterial action |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP1036146B1 (en) |
| JP (1) | JP2001526301A (en) |
| AT (1) | ATE287940T1 (en) |
| DE (2) | DE19753982A1 (en) |
| ES (1) | ES2236963T3 (en) |
| WO (1) | WO1999029815A1 (en) |
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| JP2003512511A (en) * | 1999-10-21 | 2003-04-02 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチエン | Packaging of dishwasher detergent |
| DE102009005791A1 (en) | 2009-01-22 | 2010-07-29 | Henkel Ag & Co. Kgaa | Hand dishwashing detergent with antibacterial effect |
| EP3421582A1 (en) * | 2017-06-29 | 2019-01-02 | The Procter & Gamble Company | Cleaning composition |
| EP3421580A1 (en) * | 2017-06-29 | 2019-01-02 | The Procter & Gamble Company | Cleaning composition |
| WO2020165566A1 (en) | 2019-02-11 | 2020-08-20 | Reckitt Benckiser Health Limited | Topical sanitizing compositions |
| WO2022112764A1 (en) | 2020-11-30 | 2022-06-02 | Reckitt Benckiser Health Limited | Personal care compositions |
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| GB0105342D0 (en) * | 2001-03-03 | 2001-04-18 | Selden Res Ltd | Biocidal cleaning composition |
| GB2417959A (en) * | 2004-09-11 | 2006-03-15 | Reckitt Benckiser Inc | Cleaning and sanitizing compositions |
| EP2436754A1 (en) * | 2011-09-30 | 2012-04-04 | Basf Se | Antimicrobial cleaning compound |
| BR112020005885A2 (en) | 2017-09-26 | 2020-09-29 | Ecolab Usa Inc. | antimicrobial, virucide, solid antimicrobial and solid virucide compositions, and methods for using an antimicrobial composition and inactivating a virus. |
| WO2020210789A1 (en) | 2019-04-12 | 2020-10-15 | Ecolab Usa Inc. | Hard surface cleaning solution with rapid viricidal activity |
| CA3161330A1 (en) | 2019-12-16 | 2021-06-24 | Ecolab Usa Inc. | Anionic surfactant impact on virucidal efficacy |
| JP2022026764A (en) * | 2020-07-31 | 2022-02-10 | 花王株式会社 | Virus inactivator composition |
| DE102023212239A1 (en) | 2023-12-05 | 2025-06-05 | Henkel Ag & Co. Kgaa | Boric acid-free liquid detergent |
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| WO1997028237A1 (en) * | 1996-01-31 | 1997-08-07 | Neozyme International, Inc. | Composition for cleaning grease-traps and septic tanks control |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4844891A (en) * | 1988-02-03 | 1989-07-04 | Lonza, Inc. | Admixtures of iodopropargyl compounds and a formaldehyde donor |
| JP2775915B2 (en) * | 1989-11-06 | 1998-07-16 | ライオン株式会社 | Nonionic surfactant |
| US5476614A (en) * | 1995-01-17 | 1995-12-19 | Colgate Palmolive Co. | High foaming nonionic surfactant based liquid detergent |
-
1997
- 1997-12-05 DE DE19753982A patent/DE19753982A1/en not_active Ceased
-
1998
- 1998-11-28 DE DE59812520T patent/DE59812520D1/en not_active Expired - Lifetime
- 1998-11-28 WO PCT/EP1998/007698 patent/WO1999029815A1/en not_active Ceased
- 1998-11-28 ES ES98958927T patent/ES2236963T3/en not_active Expired - Lifetime
- 1998-11-28 JP JP2000524392A patent/JP2001526301A/en active Pending
- 1998-11-28 AT AT98958927T patent/ATE287940T1/en not_active IP Right Cessation
- 1998-11-28 EP EP98958927A patent/EP1036146B1/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0670158A2 (en) * | 1994-02-14 | 1995-09-06 | Colgate-Palmolive Company | Cleansing composition |
| WO1995035364A1 (en) * | 1994-06-20 | 1995-12-28 | Unilever Plc | Improvements relating to antimicrobial cleaning compositions |
| WO1996017918A1 (en) * | 1994-12-09 | 1996-06-13 | Unilever Plc | Improvements relating to antimicrobial cleaning compositions |
| WO1997028237A1 (en) * | 1996-01-31 | 1997-08-07 | Neozyme International, Inc. | Composition for cleaning grease-traps and septic tanks control |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003512511A (en) * | 1999-10-21 | 2003-04-02 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチエン | Packaging of dishwasher detergent |
| DE102009005791A1 (en) | 2009-01-22 | 2010-07-29 | Henkel Ag & Co. Kgaa | Hand dishwashing detergent with antibacterial effect |
| WO2010084057A1 (en) | 2009-01-22 | 2010-07-29 | Henkel Ag & Co. Kgaa | Hand dishwashing agent having antibacterial effect |
| WO2019006227A1 (en) * | 2017-06-29 | 2019-01-03 | The Procter & Gamble Company | Cleaning composition |
| EP3421580A1 (en) * | 2017-06-29 | 2019-01-02 | The Procter & Gamble Company | Cleaning composition |
| WO2019006229A1 (en) * | 2017-06-29 | 2019-01-03 | The Procter & Gamble Company | Cleaning composition |
| EP3421582A1 (en) * | 2017-06-29 | 2019-01-02 | The Procter & Gamble Company | Cleaning composition |
| EP3572494A1 (en) * | 2017-06-29 | 2019-11-27 | The Procter & Gamble Company | Cleaning composition |
| US11518958B2 (en) | 2017-06-29 | 2022-12-06 | Tire Procter & Gamble Company | Cleaning composition |
| US11530371B2 (en) | 2017-06-29 | 2022-12-20 | The Procter & Gamble Company | Cleaning composition |
| US12049604B2 (en) | 2017-06-29 | 2024-07-30 | The Procter & Gamble Company | Cleaning composition |
| WO2020165566A1 (en) | 2019-02-11 | 2020-08-20 | Reckitt Benckiser Health Limited | Topical sanitizing compositions |
| WO2022112764A1 (en) | 2020-11-30 | 2022-06-02 | Reckitt Benckiser Health Limited | Personal care compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1036146B1 (en) | 2005-01-26 |
| EP1036146A1 (en) | 2000-09-20 |
| ATE287940T1 (en) | 2005-02-15 |
| ES2236963T3 (en) | 2005-07-16 |
| DE59812520D1 (en) | 2005-03-03 |
| DE19753982A1 (en) | 1999-06-10 |
| JP2001526301A (en) | 2001-12-18 |
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