EP2480646B1 - Unperfumed cleaning agent - Google Patents

Unperfumed cleaning agent Download PDF

Info

Publication number
EP2480646B1
EP2480646B1 EP10747460.3A EP10747460A EP2480646B1 EP 2480646 B1 EP2480646 B1 EP 2480646B1 EP 10747460 A EP10747460 A EP 10747460A EP 2480646 B1 EP2480646 B1 EP 2480646B1
Authority
EP
European Patent Office
Prior art keywords
cleaning agent
agent according
fatty
fatty alcohol
cleaning
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.)
Not-in-force
Application number
EP10747460.3A
Other languages
German (de)
French (fr)
Other versions
EP2480646A1 (en
Inventor
Michael Dreja
Stefan Karsten
Patrick Markiefka
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP2480646A1 publication Critical patent/EP2480646A1/en
Application granted granted Critical
Publication of EP2480646B1 publication Critical patent/EP2480646B1/en
Not-in-force legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D9/00Compositions of detergents based essentially on soap
    • C11D9/04Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
    • C11D9/22Organic compounds, e.g. vitamins
    • C11D9/26Organic compounds, e.g. vitamins containing oxygen
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/662Carbohydrates or derivatives
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/90Betaines

Definitions

  • the invention relates to a perfume-free aqueous cleaning agent for hard surfaces and / or textiles containing tall oil soap and at least one C 1 -C 6 -alcohol.
  • All-purpose cleaners have long been used in many households for cleaning hard surfaces, usually in diluted form. They have proven themselves in the removal of a variety of stains. Also means of stain removal and stain pretreatment on textiles are often used, mostly in concentrated form.
  • fragrances are often not available on the basis of renewable resources and also poorly biodegradable.
  • fragrances the components of which also have an allergenic potential at higher concentrations, are considered to be problematic.
  • US 7396808 B1 (The Clorox Company) describes hard surface cleaners consisting essentially of 0.5 to 5 weight percent alkyl polyglucoside, 0.5 to 5 weight percent ethanol, 0.05 to 1 weight percent glycerol, 0.05 to 0.4 wt .-% lemon oil or d-limonene and water, less than 0.2 wt.% Builder and optionally colorants and preservatives exist. It should be to cleaners of natural ingredients with high cleaning performance. However, the fragrances contained are not readily biodegradable and can also act as allergens. US 5080831 . US 4477361 and EP 0375474 describe detergents containing tall oil soaps.
  • a cleanser which contains tall oil soap and at least one C 1 -C 6 -alcohol has a scent which is perceived as pleasant even without the use of perfume oils and other fragrances.
  • it also has a good cleaning performance when using surfactants purely on a oleochemical basis.
  • the subject of this application is accordingly a perfume-free aqueous cleaning agent for hard surfaces and / or textiles, which 0.1 to 15 wt.% Tallölseife at least one C 1 -C 6 alcohol, and 0.1 to 12 wt.% Of at least one surfactant contains the fat-chemical base, wherein the at least one surfactant is selected on the basis of oleochemical base from the group comprising alkylpolyglycosides, fatty alcohol alkoxylates, Alkylamidoalkylamine, fatty alcohol ether sulfates and mixtures thereof.
  • the cleaning agent is suitable both for diluted application and for direct application to the surface to be cleaned.
  • a spray dispenser is used, preferably a spray dispenser with foam nozzle.
  • a further subject of this application is accordingly a product comprising a cleaning agent according to the invention and a spray dispenser, in particular a cleaning agent according to the invention and a spray dispenser with foam nozzle.
  • the cleaning agent according to the invention is preferably used for cleaning hard surfaces and / or textiles in a corresponding cleaning process.
  • a further subject of the application is therefore the use of a cleaning agent according to the invention for cleaning hard surfaces.
  • Yet another subject of this application is a method for cleaning hard surfaces, wherein in a process step, the cleaning agent according to the invention is applied to the surface to be cleaned.
  • Another object of the invention is the use of a cleaning agent according to the invention for stain removal and / or for spot pretreatment on textiles, in particular for greasy stains.
  • the indication CAS means that the following sequence of numbers is a name of the Chemical Abstracts Service .
  • the cleaning agent according to the invention contains tall oil soap. This is the product of saponification of the mixture of saturated and especially unsaturated C 18-22 fatty acids obtained from the distillation of tall oil. Such tall oil fatty acids are commercially available, for example, under the trade name Sylvatal® from Arizona Chemical. A particularly preferred tall oil soap is the sodium salt obtained by saponification from Sylvatal® 10VS.
  • the composition according to the invention contains from 0.1 to 15% by weight, preferably from 1 to 10% by weight, in particular from 2 to 8% by weight, of tall oil soap.
  • inventive composition contains at least one C 1-6 alcohol.
  • C 1-6 alcohol may be, for example, the following compounds named according to INCl:
  • Alcohol (ethanol), n-butyl alcohol, t-butyl alcohol, diethylene glycol, dipropylene glycol, glycol, hexanediol, 1,2,6-hexanetriol, hexyl alcohol, hexylene glycol, isobutoxypropanol, isopentyl diol, isopropyl alcohol (iso-propanol) , Methyl Alcohol, Methylpropanediol, Neopentyl Glycol, Pentylene Glycol, Propanediol, Propyl Alcohol (n-Propanol), Propylene Glycol.
  • ethanol, n-propanol or iso-propanol are used, in particular ethanol.
  • the C 1-6 -alcohol is preferably present in amounts of from 0.2 to 15% by weight, more preferably from 1 to 10% by weight.
  • the inventive composition further contains at least one surfactant based on oleochemical.
  • surfactants whose alkyl groups are not obtained by petrochemical means but from renewable raw materials.
  • Suitable surfactants based on oleochemicals are alkyl polyglycosides, alkylamidoalkylamines, fatty alcohol alkoxylates, fatty alcohol ether sulfates and mixtures thereof.
  • the composition according to the invention contains surfactants on a oleochemical basis in amounts of from 0.1 to 12% by weight, preferably from 0.5 to 8% by weight, in particular from 1 to 5% by weight.
  • fatty acids or fatty alcohols or their derivatives in the context of the present invention, branched or unbranched carboxylic acids or alcohols or their derivatives having preferably 6 to 22 carbon atoms.
  • the alkyl polyglycosides are nonionic surfactants. They are among the surfactants preferred in the context of the teaching according to the invention on a oleochemical basis. These are sugar surfactants, preferably of the general formula I RO (AO) a [G] x in which R is a linear or branched, saturated or unsaturated alkyl radical having 6 to 22, preferably 6 to 18, in particular 8 to 16, particularly preferably 8 to 14 carbon atoms, [G] for a glycosidically linked sugar residue and x for a number from 1 to 10 and AO for an alkyleneoxy group, for example an ethyleneoxy or Propylenoxyoli, and a for the average degree of alkoxylation of 0 to 20.
  • R is a linear or branched, saturated or unsaturated alkyl radical having 6 to 22, preferably 6 to 18, in particular 8 to 16, particularly preferably 8 to 14 carbon atoms
  • [G] for a glycosidically linked sugar residue and x for a number from
  • the group (AO) a may also contain different alkyleneoxy units, for example ethyleneoxy or propyleneoxy units, in which case a is the average total degree of alkoxylation, ie the sum of degree of ethoxylation and degree of propoxylation.
  • the alkyl radicals R 1 of the APG are linear unsaturated radicals having the stated number of carbon atoms.
  • the index number x indicates the degree of oligomerization (DP degree), ie the distribution of monoglycerides and oligoglycosides, and stands, as just described, for a number between 1 and 10.
  • alkyl glycosides having a mean degree of oligomerization x of 1.1 to 3.0 are used. From an application point of view, those alkyl glycosides whose degree of oligomerization is less than 1.7 and in particular between 1.2 and 1.6 are preferred.
  • the glycosidic sugar used is preferably xylose, but especially glucose.
  • the average degree of oligomerization x is preferably 1.2-1.5.
  • the alkyl radical is preferably in the range C8-C16 (thus n in the aforementioned formula is preferably 7-15). Very particular preference is decyl glycoside.
  • alkylamidoalkylamines are the following INCI named in accordance compounds: Cocoamphodipropionic Acid, Cocobetainamido amphopropionates, DEA-Cocoamphodipropionate, Disodium Caproamphodiacetate, Disodium Caproamphodipropionate, Disodium Capryloamphodiacetate, Disodium Capryloamphodipropionate, Disodium Cocoamphocarboxyethylhydroxypropylsulfonate, Disodium Cocoamphodiacetate, Disodium Cocoamphodipropionate, Disodium Isostearoamphodiacetate, Disodium Isostearoamphodipropionate, Disodium laureth 5 Carboxyamphodiacetate, Disodium Lauroamphodiacetate, Disodium Lauroamphodipropionate, Disodium Oleoamphodipropionate, Disodium PPG-2-Isodeceth-7 Carboxyamphodia
  • the alkylamidoalkylamine is preferably selected from the group consisting of disodium cocoamphodiacetate, disodium lauroamphodiacetate, sodium stearoamphoacetate, sodium cocoamphoacetate, disodium cocoamphodipropionate, disodium stearoamphodiacetate and mixtures thereof, and in particular preferably disodium cocoamphodiacetate (sodium cocoamphodiacetate).
  • fatty alcohol alkoxylates in agents according to the invention.
  • C 8 -C 18 -alcohol polyglycol ethers ie ethoxylated and / or propoxylated alcohols having 8 to 18 C atoms in the alkyl moiety and 2 to 15 ethylene oxide (EO) and / or propylene oxide units (PO).
  • EO ethylene oxide
  • PO propylene oxide units
  • Particular preference is given to using C 8-18 -fatty alcohol ethoxylates having 2 to 10 EO, in particular C 12-14 fatty alcohol ethoxylates having 2 to 8 EO, for example C 12-14 -fatty alcohol ethoxylate with 7 EO.
  • fatty alcohol ether sulfates C 8 -C 18 -alkyl polyglycol ether sulfates.
  • Fatty alcohol ether sulfates are products of sulfation reactions on alkoxylated alcohols.
  • the person skilled in the art generally understands, under alkoxylated alcohols, the reaction products of alkylene oxide, preferably ethylene oxide, with alcohols, preferably in the context of the present invention, the longer-chain alcohols (fatty alcohols).
  • n moles of ethylene oxide and one mole of alcohol form a complex mixture of addition products of different degrees of ethoxylation.
  • a further embodiment consists in the use of mixtures of the alkylene oxides, preferably of the mixture of ethylene oxide and propylene oxide.
  • ethoxylated fatty alcohols 0.5 to 4 mol of EO, preferably 1 to 2.5 mol of EO.
  • a particularly preferred fatty alcohol ether sulfate is, for example, C 12-14 fatty alcohol ether sulfate with 2 EO.
  • the anionic surfactants are preferably used as sodium salts, but may also be present as other alkali metal or alkaline earth metal salts, for example magnesium salts, and in the form of ammonium or mono-, di-, tri- or tetraalkylammonium salts, in the case of the sulfonates also in the form their corresponding acid, eg dodecylbenzenesulfonic acid.
  • the agent according to the invention may also contain acids or bases or volatile alkali.
  • the volatile alkali used is ammonia and / or alkanolamines, which may contain up to 9 C atoms in the molecule.
  • alkanolamines the ethanolamines are preferred and of these in turn the monoethanolamine.
  • the content of ammonia and / or alkanolamine is preferably 0.01 to 2 wt .-%; ammonia is particularly preferably used.
  • the cleaning agents according to the invention may also contain small amounts of bases.
  • Preferred bases are selected from the group of alkali and alkaline earth metal hydroxides and carbonates, in particular the alkali metal hydroxides, of which potassium hydroxide, sodium hydroxide and mixtures thereof are particularly preferred.
  • Alkaline agents may additionally contain carboxylic acid in addition to the volatile alkali, wherein the equivalent ratio of amine and / or ammonia to carboxylic acid is preferably between 1: 0.9 and 1: 0.1.
  • Suitable carboxylic acids having up to 6 carbon atoms which may be mono-, di- or polycarboxylic acids.
  • the content of carboxylic acid is preferably between 0.01 and 2.7% by weight, in particular between 0.01 and 0.9% by weight.
  • carboxylic acids examples include acetic acid, glycolic acid, lactic acid, citric acid, succinic acid, adipic acid, malic acid, tartaric acid and gluconic acid, of which preferably acetic acid, citric acid and lactic acid are used.
  • Citric acid is particularly preferably used.
  • composition according to the invention preferably has a pH of between 7 and 11.5.
  • composition according to the invention may contain further ingredients usually used in cleaning agents.
  • these are selected from the group consisting of dyes, co-surfactants, disinfectants, pH buffers, thickeners, organic and inorganic salts, other solvents, preferably those which are generally perceived as fragrant, optical brighteners, antioxidants, opacifiers, hydrotropes, Abrasives, preservatives, oxidizing agents, insecticides, enzymes, probiotic ingredients, skin protection and skin care products, and mixtures thereof.
  • the agent according to the invention may contain, in addition to the ingredients mentioned, further surface-active substances.
  • Suitable surface-active substances for the compositions according to the invention are surfactants from the classes of anionic, nonionic, cationic and amphoteric surfactants.
  • surfactants with proportions of renewable raw materials are also used here.
  • Suitable anionic surfactants are preferably C 8 -C 20 -alkanesulfonates, C 8 -C 18 -monoalkyl sulfates and sulfosuccinic mono- and di-C 8 -C 18 -alkyl esters.
  • C 8 -C 18 - ⁇ -olefinsulfonates sulfonated C 8 -C 18 fatty acids, C 8 -C 22 -Carbonklareamidethersulfate, C 8 -C 18 -Alkylpolyglykolethercarboxylate, C 8 -C 18 -N-Acyltauride, C 8 -C 18 -N-sarcosinates and C 8 -C 18 -alkyl isethionates or mixtures thereof.
  • the anionic surfactants are preferably used as sodium salts, but may also be present as other alkali or alkaline earth metal salts, for example magnesium salts, and in the form of ammonium or mono-, di-, tri- or tetraalkylammonium salts, in the case of the sulfonates also in the form their corresponding acid.
  • examples of such surfactants are sodium cocoalkyl sulfate, sodium sec-alkanesulfonate having about 15 carbon atoms and sodium dioctylsulfosuccinate.
  • the agent according to the invention is free of linear alkylbenzenesulfonate surfactants (LAS), which have hitherto been used frequently in cleaning agents as anionic surfactants.
  • LAS linear alkylbenzenesulfonate surfactants
  • Particularly suitable nonionic surfactants are C 8 -C 18 -carboxylic acid polyglycol esters having 2 to 15 EO, for example tallow fatty acid + 6-EO esters, ethoxylated fatty acid amides having 12 to 18 C atoms in the fatty acid moiety and 2 to 8 EO, for example lauric acid diethanolamide, and long-chain ones Mention is made of amine oxides having 14 to 20 carbon atoms, such as the cocoalkyldimethylamine oxide.
  • Suitable amphoteric surfactants are, for example, betaines of the formula (R ii ) (R iii ) (R v ) N + CH 2 COO - , in which R "is an alkyl radical optionally interrupted by hetero atoms or heteroatom groups having 8 to 25, preferably 10 to 21 carbon atoms and R iii and Ri v are identical or different alkyl radicals having 1 to 3 carbon atoms, in particular C 10 -C 18 -alkyl-dimethylcarboxymethylbetain and C 11 -C 17 -alkylamidopropyl-dimethylcarboxymethylbetain.
  • Suitable cationic surfactants include the quaternary ammonium compounds of the formula (R v ) (R vi ) (R vii ) (R viii ) N + X - , in which R v to R viii for four identical or different, in particular two long and two short-chain, alkyl radicals and X - represent an anion, in particular a halide ion, for example, didecyl-dimethyl-ammonium chloride, alkyl-benzyl-didecyl-ammonium chloride and mixtures thereof.
  • viscosity regulators commonly used in detergents and cleaning agents are suitable, for example organic natural thickeners (agar-agar, carrageenan, tragacanth, gum arabic, alginates, pectins, Polyols, guar gum, locust bean gum, starch, dextrins, gelatin, casein), organic modified natural products (carboxymethyl cellulose and other cellulose ethers, hydroxyethyl and propyl cellulose and the like, gum ethers), organic fully synthetic thickeners (polyacrylic and polymethacrylic compounds, vinyl polymers, Polycarboxylic acids, polyethers, polyimines, polyamides) and inorganic thickeners (polysilicic acids, clay minerals such as montmorillonites, zeolites, silicic acids).
  • organic natural thickeners agar-agar, carrageenan, tragacanth, gum arabic, alginates, pectins, Polyols, guar gum, locust
  • the agent according to the invention is free of thickeners.
  • the viscosity of the composition according to the invention is preferably 0.4 to 400 mPas (Brookfield LVDV 2+ with small sample adapter, spindle 31, 30 rpm, 20 ° C., undiluted product).
  • the cleaning agent therefore contains one or more antimicrobial agents, preferably in an amount of 0.01 to 2% by weight, preferably 0.02 to 0 , 9 wt .-%, in particular 0.05 to 0.5 wt .-%, particularly preferably 0.1 to 0.4 wt .-%, most preferably 0.3 wt .-%.
  • disinfection, sanitation, antimicrobial action and antimicrobial agent have the usual meaning in the context of the teaching of the invention, the example of KH Wall conferenceußer in "Practice of Sterilization, Disinfection - Conservation: Germ Identification - Plant Hygiene” (5th edition - Stuttgart, New York: Thieme, 1995 ) is reproduced. While disinfection in the narrower sense of the medical practice means the killing of - in theory all - infectious germs, sanitation is to be understood as the greatest possible elimination of all - including the saprophytic - normally harmless to humans saprophytic - germs.
  • the extent of disinfection or sanitation depends on the antimicrobial effect of the applied agent, which decreases with decreasing content of antimicrobial agent or increasing dilution of the agent for use.
  • antimicrobial agents from the groups of alcohols, aldehydes, antimicrobial acids or their salts, carboxylic esters, acid amides, phenols, phenol derivatives, diphenyls, diphenylalkanes, urea derivatives, oxygen, nitrogen acetals and formals, benzamidines, isothiazoles and their derivatives are suitable according to the invention
  • Derivatives such as isothiazolines and isothiazolinones, phthalimide derivatives, pyridine derivatives, antimicrobial surface-active compounds, guanidines, antimicrobial amphoteric compounds, quinolines, 1,2-dibromo-2,4-dicyanobutane, iodo-2-propynyl-butyl-carbamate, iodine,
  • Preferred antimicrobial agents are preferably selected from the group comprising ethanol, n-propanol, i-propanol, 1,3-butanediol, phenoxyethanol, 1,2-propylene glycol, glycerol, undecylenic acid, citric acid, lactic acid, benzoic acid, salicylic acid, thymol, 2- Benzyl 4-chlorophenol, 2,2'-methylenebis (6-bromo-4-chlorophenol), 2,4,4'-trichloro-2'-hydroxydiphenyl ether, N- (4-chlorophenyl) -N- ( 3,4-dichlorophenyl) urea, N, N '- (1,10-decanediyldi-1-pyridinyl-4-ylidene) bis (1-octanamine) dihydrochloride, N, N'-bis (4- Chlorophenyl) -3,12-diimino-2,4,11,13
  • Preferred antimicrobial surface active quaternary compounds contain an ammonium, sulfonium, phosphonium, iodonium or arsonium group, as for example KH Wallrobußer in "Practice of Sterilization, Disinfection - Conservation: Germ Identification - Plant Hygiene” (5th edition - Stuttgart, New York: Thieme, 1995 ) describes.
  • antimicrobially effective essential oils can be used, which at the same time provide for a scenting of the cleaning agent.
  • particularly preferred antimicrobial agents are selected from the group comprising salicylic acid, quaternary surfactants, in particular benzalkonium chloride, peroxo compounds, in particular hydrogen peroxide, alkali metal hypochlorite and mixtures thereof.
  • Preservatives may also be included in compositions of the invention. As such, essentially the substances mentioned in the antimicrobial agents can be used.
  • composition according to the invention may additionally contain skin protection and skin care agents.
  • skin care agents including bisabolol, allantoin, vitamins such as panthenol, natural oils such as almond oil, plant extracts such as marigold, aloe vera, nourishing wax dispersions, nourishing polymers and other used in cosmetic care and conditioning agents and Count mixtures.
  • the agent can be sprayed onto the surface to be cleaned or applied in the form of a foam.
  • a manually activated spray dispenser in particular selected from the group comprising aerosol spray dispensers, pressure-building spray dispensers, pump spray dispensers and trigger spray dispensers, in particular pump spray dispensers and trigger spray dispensers with a container made of polyethylene, polypropylene or polyethylene terephthalate.
  • trigger bottles are offered for example by the company Afa-Polytec.
  • the spray head is preferably equipped with a foam nozzle.
  • pump foam dispensers such as those offered by the company Airspray or the Daiwa Can Company, are also suitable.
  • the agent can also be added with the addition of a suitable propellant (eg n-butane, a propane / butane mixture, carbon dioxide, nitrogen, or a CO 2 / N 2 mixture) are charged into a corresponding Aerosolsprühflasche.
  • a suitable propellant eg n-butane, a propane / butane mixture, carbon dioxide, nitrogen, or a CO 2 / N 2 mixture
  • a suitable propellant eg n-butane, a propane / butane mixture, carbon dioxide, nitrogen, or a CO 2 / N 2 mixture
  • a suitable propellant eg n-butane, a propane / butane mixture, carbon dioxide, nitrogen, or a CO 2 / N 2 mixture
  • such a spray dispenser is less preferred.
  • a further subject of the invention is accordingly a product comprising a cleaning agent according to the invention and a spray dispenser, in particular a cleaning agent according to the invention and a trigger bottle with a foam nozzle.
  • the agents according to the invention are preferably used for cleaning hard surfaces.
  • Another subject of the invention is therefore the use of a cleaning agent according to the invention for cleaning hard surfaces.
  • Hard surfaces in the context of this application are windows, mirrors and other glass surfaces, surfaces made of ceramic, plastic, metal or wood and lacquered wood, which are found in household and commercial, such as bathroom ceramics, kitchen surfaces or floors.
  • the detergent is diluted before use with water or, in particular by means of a spray dispenser, applied undiluted.
  • the cleaning agent according to the invention is applied in one process step to the surface to be cleaned.
  • the agents according to the invention are used for stain removal and / or for spot pretreatment on textiles.
  • they are particularly suitable for the treatment of fatty stains.
  • a further subject of the invention is accordingly the use of a cleaning agent according to the invention for stain removal and / or for spot pretreatment on textiles, in particular for greasy stains.
  • the fragrance of the formulations was scented by an expert panel of five trained persons on the concentrated product as well as in the application concentration and the fragrance impression was rated on a grading scale from 1 (very good) to 7 (unpleasant).
  • perfume-free formulations according to the invention left an equally good or even more positive scent impression than the perfume-containing comparative formulation.

Description

Die Erfindung betrifft ein parfümfreies wässriges Reinigungsmittel für harte Oberflächen und/oder Textilien, das Tallölseife und mindestens einen C1-C6-Alkohol enthält.The invention relates to a perfume-free aqueous cleaning agent for hard surfaces and / or textiles containing tall oil soap and at least one C 1 -C 6 -alcohol.

Allzweckreiniger kommen schon seit langem in vielen Haushalten zur Reinigung harter Oberflächen zum Einsatz, meist in verdünnter Form. Sie haben sich bei der Entfernung einer Vielzahl von Anschmutzungen bewährt. Auch Mittel zur Fleckentfernung und zur Fleckenvorbehandlung auf Textilien kommen oft zur Anwendung, meist in konzentrierter Form.All-purpose cleaners have long been used in many households for cleaning hard surfaces, usually in diluted form. They have proven themselves in the removal of a variety of stains. Also means of stain removal and stain pretreatment on textiles are often used, mostly in concentrated form.

Es ist wünschenswert und entspricht mittlerweile auch gesetzlichen Vorschriften und Normen, dass die Verwendung von Wasch- und Reinigungsmitteln einen möglichst geringen negativen Einfluss auf die Umwelt ausübt. Beispielsweise schreibt die EU-Detergenzienverordnung vor, dass bei jedem heute in Waschmitteln eingesetzte Tensid der Primärabbau mindestens 80% betragen soll, der vollständige biologische Abbau (nach 28 Tagen) mindestens 60 %. Die bislang wegen ihrer guten Reinigungsleistung häufig eingesetzten Tenside auf petrochemischer Basis, beispielsweise lineare Alkylbenzolsulfonate (LAS), sind jedoch nur schlecht anaerob abbaubar. Es wäre also vorteilhaft, Formulierungen zu finden, deren Tenside und auch andere Aktivsubstanzen vollständig auf Basis nachwachsender Rohstoffe hergestellt sind.It is desirable and now also complies with legal regulations and standards that the use of detergents and cleaners has the least negative impact on the environment. For example, the EU Detergents Regulation requires that for each surfactant used today in detergents, primary degradation should be at least 80% and full biodegradation (after 28 days) at least 60%. However, the petrochemical-based surfactants frequently used because of their good cleaning performance, for example linear alkylbenzenesulfonates (LAS), are only poorly degradable anaerobically. It would therefore be advantageous to find formulations whose surfactants and also other active substances are completely prepared on the basis of renewable raw materials.

Dabei besteht die Herausforderung darin, keine Einbußen bezüglich der Reinigungsleistung entstehen zu lassen. Tenside auf Basis nachwachsender Rohstoffe sind gut bekannt, weisen aber oft keine ausreichende Reinigungsleistung auf, so dass sie in der Regel mit Tensiden auf petrochemischer Basis kombiniert werden müssen.The challenge is not to sacrifice any cleaning performance. Surfactants based on renewable raw materials are well known, but often do not have sufficient cleaning performance, so they must be combined with surfactants on a petrochemical basis in the rule.

Weiterhin sind auch die übrigen Inhaltsstoffe, etwa Lösemittel, Duft- oder Hilfsstoffe, häufig nicht auf der Basis nachwachsender Rohstoffe verfügbar und auch schlecht biologisch abbaubar. Insbesondere die Duftstoffe, deren Komponenten bei höheren Konzentrationen teilweise auch ein allergenes Potential aufweisen, werden dabei als problematisch angesehen.Furthermore, the other ingredients, such as solvents, fragrances or auxiliaries, are often not available on the basis of renewable resources and also poorly biodegradable. In particular, the fragrances, the components of which also have an allergenic potential at higher concentrations, are considered to be problematic.

Es bestand daher der Wunsch nach einem Reinigungsmittel für harte Oberflächen auf der Basis eines höheren Anteils an nachwachsenden Rohstoffen, das dennoch eine gute Reinigungsleistung aufweist; dieses Mittel sollte zudem frei von Parfümölen und anderen Duftstoffen sein und dabei einen als angenehm wahrgenommenen Duft besitzen.Therefore, there has been a desire for a hard surface cleaner based on a higher proportion of renewable resources yet having a good cleaning performance; This remedy should also be free from perfume oils and other fragrances and have a pleasant smell.

US 7396808 B1 (The Clorox Company) beschreibt Reinigungsmittel für harte Oberflächen, die im wesentlichen aus 0,5 bis 5 Gew.-% Alkylpolyglucosid, 0,5 bis 5 Gew.-% Ethanol, 0,05 bis 1 Gew.% Glycerin, 0,05 bis 0,4 Gew.-% Zitronenöl oder d-Limonen sowie Wasser, weniger als 0,2 Gew.% Builder und gegebenenfalls Farbstoffen und Konservierungsmitteln bestehen. Es soll sich dabei um Reinigungsmittel aus natürlichen Inhaltsstoffen mit dennoch hoher Reinigungsleistung handeln. Die enthaltenen Duftstoffe sind allerdings nicht gut biologisch abbaubar und können zudem als Allergene wirken. US 5080831 , US 4477361 und EP 0375474 beschreiben Reinigungsmittel, die u.a. Tallölseifen enthalten. US 7396808 B1 (The Clorox Company) describes hard surface cleaners consisting essentially of 0.5 to 5 weight percent alkyl polyglucoside, 0.5 to 5 weight percent ethanol, 0.05 to 1 weight percent glycerol, 0.05 to 0.4 wt .-% lemon oil or d-limonene and water, less than 0.2 wt.% Builder and optionally colorants and preservatives exist. It should be to cleaners of natural ingredients with high cleaning performance. However, the fragrances contained are not readily biodegradable and can also act as allergens. US 5080831 . US 4477361 and EP 0375474 describe detergents containing tall oil soaps.

Überraschend wurde nun gefunden, dass ein Reinigungsmittel, welches Tallölseife und mindestens einen C1-C6-Alkohol enthält, auch ohne den Einsatz von Parfümölen und anderen Duftstoffen einen als angenehm empfundenen Duft aufweist. Zudem weist es auch beim Einsatz von Tensiden rein auf fettchemischer Basis eine gute Reinigungsleistung auf.Surprisingly, it has now been found that a cleanser which contains tall oil soap and at least one C 1 -C 6 -alcohol has a scent which is perceived as pleasant even without the use of perfume oils and other fragrances. In addition, it also has a good cleaning performance when using surfactants purely on a oleochemical basis.

Gegenstand dieser Anmeldung ist dementsprechend ein parfümfreies wässriges Reinigungsmittel für harte Oberflächen und/oder Textilien, welches 0,1 bis 15 Gew.% Tallölseife mindestens einen C1-C6-Alkohol , und 0,1 bis 12 Gew.% mindestens eines Tensids auf fettchemischer Basis enthält, wobei das mindestens eine Tensid auf fettchemischer Basis ausgewählt ist aus der Gruppe umfassend Alkylpolyglycoside, Fettalkoholalkoxylate, Alkylamidoalkylamine, Fettalkoholethersulfate sowie Mischungen derselben.The subject of this application is accordingly a perfume-free aqueous cleaning agent for hard surfaces and / or textiles, which 0.1 to 15 wt.% Tallölseife at least one C 1 -C 6 alcohol, and 0.1 to 12 wt.% Of at least one surfactant contains the fat-chemical base, wherein the at least one surfactant is selected on the basis of oleochemical base from the group comprising alkylpolyglycosides, fatty alcohol alkoxylates, Alkylamidoalkylamine, fatty alcohol ether sulfates and mixtures thereof.

Das Reinigungsmittel eignet sich sowohl zur verdünnten Anwendung als auch zur direkten Applikation auf die zu reinigende Oberfläche. Hierzu wird vorzugsweise ein Sprühspender verwendet, bevorzugt ein Sprühspender mit Schaumdüse.The cleaning agent is suitable both for diluted application and for direct application to the surface to be cleaned. For this purpose, preferably a spray dispenser is used, preferably a spray dispenser with foam nozzle.

Ein weiterer Gegenstand dieser Anmeldung ist dementsprechend ein Erzeugnis aus einem erfindungsgemäßen Reinigungsmittel und einem Sprühspender, insbesondere aus einem erfindungsgemäßen Reinigungsmittel und einem Sprühspender mit Schaumdüse.A further subject of this application is accordingly a product comprising a cleaning agent according to the invention and a spray dispenser, in particular a cleaning agent according to the invention and a spray dispenser with foam nozzle.

Das erfindungsgemäße Reinigungsmittel wird bevorzugt zur Reinigung harter Oberflächen und/oder von Textilien in einem entsprechenden Reinigungsverfahren verwendet. Ein weiterer Anmeldungsgegenstand ist daher die Verwendung eines erfindungsgemäßen Reinigungsmittels zur Reinigung harter Oberflächen. Noch ein weiterer Gegenstand dieser Anmeldung ist ein Verfahren zur Reinigung harter Oberflächen, bei dem in einem Verfahrensschritt das erfindungsgemäße Reinigungsmittel auf die zu reinigende Oberfläche aufgetragen wird. Ebenfalls ein weiterer Anmeldungsgegenstand ist die Verwendung eines erfindungsgemäßen Reinigungsmittels zur Fleckentfernung und/oder zur Fleckenvorbehandlung auf Textilien, insbesondere bei fetthaltigen Flecken.The cleaning agent according to the invention is preferably used for cleaning hard surfaces and / or textiles in a corresponding cleaning process. A further subject of the application is therefore the use of a cleaning agent according to the invention for cleaning hard surfaces. Yet another subject of this application is a method for cleaning hard surfaces, wherein in a process step, the cleaning agent according to the invention is applied to the surface to be cleaned. Another object of the invention is the use of a cleaning agent according to the invention for stain removal and / or for spot pretreatment on textiles, in particular for greasy stains.

Stoffe, die auch als Inhaltsstoffe von kosmetischen Mitteln dienen, werden nachfolgend ggf. gemäß der International Nomenclature Cosmetic Ingredient (INCI)-Nomenklatur bezeichnet. Chemische Verbindungen tragen eine INCl-Bezeichnung in englischer Sprache, pflanzliche Inhaltsstoffe werden ausschließlich nach Linne in lateinischer Sprache aufgeführt, sogenannte Trivialnamen wie "Wasser", "Honig" oder "Meersalz" werden ebenfalls in lateinischer Sprache angegeben. Die INCl-Bezeichnungen sind dem International Cosmetic Ingredient Dictionary and Handbook - Seventh Edition (1997) zu entnehmen, das von The Cosmetic, Toiletry, and Fragrance Association (CTFA), 1101 17th Street, NW, Suite 300, Washington, DC 20036, USA , herausgegeben wird und mehr als 9.000 INCl-Bezeichnungen sowie Verweise auf mehr als 37.000 Handelsnamen und technische Bezeichnungen einschließlich der zugehörigen Distributoren aus über 31 Ländern enthält. Das International Cosmetic Ingredient Dictionary and Handbook ordnet den Inhaltsstoffen eine oder mehrere chemische Klassen (Chemical Classes), beispielsweise Polymeric Ethers, und eine oder mehrere Funktionen (Functions), beispielsweise Surfactants - Cleansing Agents, zu, die es wiederum näher erläutert und auf die nachfolgend ggf. ebenfalls Bezug genommen wird.Substances which also serve as ingredients of cosmetic products are referred to below, where appropriate, according to the International Nomenclature Cosmetic Ingredient (INCI) nomenclature. Chemical compounds carry an INCL name in English, plant ingredients are listed only after Linne in Latin, so-called trivial names such as "water", "honey" or "sea salt" are also given in Latin. The INCL designations are the International Cosmetic Ingredient Dictionary and Handbook - Seventh Edition (1997), published by The Cosmetic, Toiletry and Fragrance Association (CTFA), 1101 17th Street, NW, Suite 300, Washington, DC, 20036, USA , and contains more than 9,000 INCL names, as well as references to more than 37,000 trade names and technical names, including related distributors from over 31 countries. The International Cosmetic Ingredient Dictionary and Handbook assigns to the ingredients one or more chemical classes , such as polymeric ethers, and one or more functions , such as surfactants-cleansing agents , which are further explained and discussed below possibly also referred to.

Die Angabe CAS bedeutet, dass es sich bei der nachfolgenden Zahlenfolge um eine Bezeichnung des Chemical Abstracts Service handelt.The indication CAS means that the following sequence of numbers is a name of the Chemical Abstracts Service .

Tallölseifetall oil soap

Das erfindungsgemäße Reinigungsmittel enthält Tallölseife. Hierbei handelt es sich um das Produkt der Verseifung des bei der Destillation von Tallöl erhaltenen Gemischs aus gesättigten und vor allem ungesättigten C18-22-Fettsäuren. Solche Tallölfettsäuren sind beispielsweise unter dem Handelsnamen Sylvatal® von Arizona Chemical kommerziell erhältlich. Eine besonders bevorzugte Tallölseife ist das durch Verseifung aus Sylvatal® 10VS gewonnene Natriumsalz. Das erfindungsgemäße Mittel enthält 0,1 bis 15 Gew.-%, bevorzugt 1 bis 10 Gew.-%, insbesondere 2 bis 8 Gew.-%, Tallölseife.The cleaning agent according to the invention contains tall oil soap. This is the product of saponification of the mixture of saturated and especially unsaturated C 18-22 fatty acids obtained from the distillation of tall oil. Such tall oil fatty acids are commercially available, for example, under the trade name Sylvatal® from Arizona Chemical. A particularly preferred tall oil soap is the sodium salt obtained by saponification from Sylvatal® 10VS. The composition according to the invention contains from 0.1 to 15% by weight, preferably from 1 to 10% by weight, in particular from 2 to 8% by weight, of tall oil soap.

C1-C6-AlkoholC 1 -C 6 alcohol

Weiterhin enthält das erfindungsgemäße Mittel mindestens einen C1-6-Alkohol. Hierbei kann es sich beispielsweise um die folgenden gemäß INCl benannten Verbindungen handeln:Furthermore, the inventive composition contains at least one C 1-6 alcohol. These may be, for example, the following compounds named according to INCl:

Alcohol (Ethanol), n-Butyl Alcohol, t-Butyl Alcohol, Diethylene Glycol, Dipropylene Glycol, Glycol, Hexanediol, 1,2,6-Hexanetriol, Hexyl Alcohol, Hexylene Glycol, Isobutoxypropanol, Isopentyldiol, Isopropyl Alcohol (iso-Propanol), Methyl Alcohol, Methylpropanediol, Neopentyl Glycol, Pentylene Glycol, Propanediol, Propyl Alcohol (n-Propanol), Propylene Glycol.Alcohol (ethanol), n-butyl alcohol, t-butyl alcohol, diethylene glycol, dipropylene glycol, glycol, hexanediol, 1,2,6-hexanetriol, hexyl alcohol, hexylene glycol, isobutoxypropanol, isopentyl diol, isopropyl alcohol (iso-propanol) , Methyl Alcohol, Methylpropanediol, Neopentyl Glycol, Pentylene Glycol, Propanediol, Propyl Alcohol (n-Propanol), Propylene Glycol.

Vorzugsweise werden Ethanol, n-Propanol oder iso-Propanol eingesetzt, insbesondere Ethanol. Der C1-6-Alkohol ist vorzugsweise in Mengen von 0,2 bis 15 Gew.-%, besonders bevorzugt 1 bis 10 Gew.-%, enthalten.Preferably, ethanol, n-propanol or iso-propanol are used, in particular ethanol. The C 1-6 -alcohol is preferably present in amounts of from 0.2 to 15% by weight, more preferably from 1 to 10% by weight.

Tensid auf fettchemischer BasisSurfactant based on oleochemicals

Das erfindungsgemäße Mittel enthält weiterhin mindestens ein Tensid auf fettchemischer Basis. Hierbei handelt es sich um Tenside, deren Alkylgruppen nicht auf petrochemischem Weg, sondern aus nachwachsenden Rohstoffen gewonnen werden.The inventive composition further contains at least one surfactant based on oleochemical. These are surfactants whose alkyl groups are not obtained by petrochemical means but from renewable raw materials.

Als Tenside auf fettchemischer Basis eignen sich Alkylpolyglykoside, Alkylamidoalkylamine, Fettalkoholalkoxylate, Fettalkoholethersulfate sowie Gemische derselben. Das erfindungsgemäße Mittel enthält Tenside auf fettchemischer Basis in Mengen von 0,1 bis 12 Gew.-%, vorzugsweise 0,5 bis 8 Gew.-%, insbesondere 1 bis 5 Gew.-%.Suitable surfactants based on oleochemicals are alkyl polyglycosides, alkylamidoalkylamines, fatty alcohol alkoxylates, fatty alcohol ether sulfates and mixtures thereof. The composition according to the invention contains surfactants on a oleochemical basis in amounts of from 0.1 to 12% by weight, preferably from 0.5 to 8% by weight, in particular from 1 to 5% by weight.

Im Rahmen der vorliegenden Erfindung stehen Fettsäuren bzw. Fettalkohole bzw. deren Derivate -soweit nicht anders angegeben - stellvertretend für verzweigte oder unverzweigte Carbonsäuren bzw. Alkohole bzw. deren Derivate mit vorzugsweise 6 bis 22 Kohlenstoffatomen.In the context of the present invention, fatty acids or fatty alcohols or their derivatives-unless stated otherwise-represent branched or unbranched carboxylic acids or alcohols or their derivatives having preferably 6 to 22 carbon atoms.

AlkylpolyglykosideAlkylpolyglykoside

Die Alkylpolyglykoside (APG) sind nichtionische Tenside. Sie zählen zu den im Rahmen der erfindungsgemäßen Lehre bevorzugten Tensiden auf fettchemischer Basis. Es handelt sich hierbei um Zuckertenside, die vorzugsweise der allgemeinen Formel I

        RO(AO)a[G]x

genügen, in der R für einen linearen oder verzweigten, gesättigten oder ungesättigten Alkylrest mit 6 bis 22, vorzugsweise 6 bis 18, insbesondere 8 bis 16, besonders bevorzugt 8 bis 14 Kohlenstoffatomen, [G] für einen glykosidisch verknüpften Zuckerrest und x für eine Zahl von 1 bis 10 sowie AO für eine Alkylenoxygruppe, z.B. eine Ethylenoxy- oder Propylenoxygruppe, und a für den mittleren Alkoxylierungsgrad von 0 bis 20 stehen. Hierbei kann die Gruppe (AO)a auch verschiedene Alkylenoxyeinheiten enthalten, z.B. Ethylenoxy- oder Propylenoxyeinheiten, wobei es sich dann bei a um den mittleren Gesamtalkoxylierungsgrad, d.h. die Summe aus Ethoxylierungsund Propoxylierungsgrad, handelt. Soweit nachfolgend nicht näher bzw. anders ausgeführt, handelt es sich bei den Alkylresten R1 der APG um lineare ungesättigte Reste mit der angegebenen Zahl an Kohlenstoffatomen. Die Indexzahl x gibt den Oligomerisierungsgrad (DP-Grad) an, d.h. die Verteilung von Mono- und Oligoglykosiden, und steht, wie gerade beschrieben, für eine Zahl zwischen 1 und 10. Während x in einer gegebenen Verbindung stets ganzzahlig sein muß und hier vor allem die Werte x = 1 bis 6 annehmen kann, ist der Wert x für ein bestimmtes Alkylglykosid eine analytisch ermittelte rechnerische Größe, die meistens eine gebrochene Zahl darstellt. Vorzugsweise werden Alkylglykoside mit einem mittleren Oligomerisierungsgrad x von 1,1 bis 3,0 eingesetzt. Aus anwendungstechnischer Sicht sind solche Alkylglykoside bevorzugt, deren Oligomerisierungsgrad kleiner als 1,7 ist und insbesondere zwischen 1,2 und 1,6 liegt. Als glykosidischer Zucker wird vorzugsweise Xylose, insbesondere aber Glucose verwendet.
The alkyl polyglycosides (APG) are nonionic surfactants. They are among the surfactants preferred in the context of the teaching according to the invention on a oleochemical basis. These are sugar surfactants, preferably of the general formula I

RO (AO) a [G] x

in which R is a linear or branched, saturated or unsaturated alkyl radical having 6 to 22, preferably 6 to 18, in particular 8 to 16, particularly preferably 8 to 14 carbon atoms, [G] for a glycosidically linked sugar residue and x for a number from 1 to 10 and AO for an alkyleneoxy group, for example an ethyleneoxy or Propylenoxygruppe, and a for the average degree of alkoxylation of 0 to 20. In this case, the group (AO) a may also contain different alkyleneoxy units, for example ethyleneoxy or propyleneoxy units, in which case a is the average total degree of alkoxylation, ie the sum of degree of ethoxylation and degree of propoxylation. Unless otherwise stated below, the alkyl radicals R 1 of the APG are linear unsaturated radicals having the stated number of carbon atoms. The index number x indicates the degree of oligomerization (DP degree), ie the distribution of monoglycerides and oligoglycosides, and stands, as just described, for a number between 1 and 10. While x in a given compound must always be integer and here before For all given values x = 1 to 6, the value x for a given alkyl glycoside is an analytically determined arithmetic variable, which usually represents a fractional number. Preferably, alkyl glycosides having a mean degree of oligomerization x of 1.1 to 3.0 are used. From an application point of view, those alkyl glycosides whose degree of oligomerization is less than 1.7 and in particular between 1.2 and 1.6 are preferred. The glycosidic sugar used is preferably xylose, but especially glucose.

Besonders bevorzugte APG können z.B. mit folgender Formel (II) beschrieben werden:

Figure imgb0001
Particularly preferred APG can be described, for example, by the following formula (II):
Figure imgb0001

Der durchschnittliche Oligomerisationsgrad x beträgt dabei vorzugsweise 1,2-1,5. Der Alkyl-Rest liegt vorzugsweise im Bereich C8-C16 (somit beträgt n in vorgenannter Formel vorzugsweise 7-15). Ganz besonders bevorzugt ist Decylglycosid.The average degree of oligomerization x is preferably 1.2-1.5. The alkyl radical is preferably in the range C8-C16 (thus n in the aforementioned formula is preferably 7-15). Very particular preference is decyl glycoside.

Alkylamidoalkylaminealkylamidoalkylamines

Eine weitre Klasse von Tensiden auf fettchemischer Basis sind die Alkylamidoalkylamine. Die Alkylamidoalkylamine (INCl Alkylamido Alkylamines) sind Amphotenside und gehorchen Formel (III),

        R1-CO-NR2-(CH2)iN(R3)-(CH2CH2O)j-(CH2)k-[CH(OH)]l-CH2-Z-OM     (III)

in der

R1
ein gesättigter oder ungesättigter C6-22-Alkylrest, vorzugsweise C8-18-Alkylrest, insbesondere ein gesättigter C10-16-Alkylrest, beispielsweise ein gesättigter C12-14-Alkylrest,
R2
ein Wasserstoffatom H oder ein C1-4-Alkylrest, vorzugsweise H,
i
eine Zahl von 1 bis 10, vorzugsweise 2 bis 5, insbesondere 2 oder 3,
R3
ein Wasserstoffatom H oder CH2COOM (zu M s.u.),
j
eine Zahl von 1 bis 4, vorzugsweise 1 oder 2, insbesondere 1,
k
eine Zahl von 0 bis 4, vorzugsweise 0 oder 1,
l
0 oder 1, wobei k = 1 ist, wenn l = 1 ist,
Z
CO, SO2, OPO(OR4) oder P(O)(OR4), wobei R4 ein C1-4-Alkylrest oder M (s.u.) ist, und
M
ein Wasserstoff, ein Alkalimetall, ein Erdalkalimetall oder ein protoniertes Alkanolamin, z.B. protoniertes Mono-, Di- oder Triethanolamin, ist.
Another class of surfactants based on oleochemicals are the alkylamidoalkylamines. The alkylamidoalkylamines (INCl alkylamido alkylamines) are amphoteric surfactants and obey formula (III),

R 1 -CO-NR 2 - (CH 2 ) i N (R 3 ) - (CH 2 CH 2 O) j - (CH 2 ) k - [CH (OH)] l -CH 2 -Z-OM (III )

in the
R 1
a saturated or unsaturated C 6-22 alkyl, preferably C 8-18 alkyl group, preferably a saturated C 10-16 alkyl group, for example a saturated C 12-14 alkyl group,
R 2
a hydrogen atom H or a C 1-4 -alkyl radical, preferably H,
i
a number from 1 to 10, preferably 2 to 5, in particular 2 or 3,
R 3
a hydrogen atom H or CH 2 COOM (to M su),
j
a number from 1 to 4, preferably 1 or 2, in particular 1,
k
a number from 0 to 4, preferably 0 or 1,
l
0 or 1, where k = 1 when l = 1,
Z
CO, SO 2 , OPO (OR 4 ) or P (O) (OR 4 ), wherein R 4 is a C 1-4 alkyl radical or M (su), and
M
a hydrogen, an alkali metal, an alkaline earth metal or a protonated alkanolamine, for example protonated mono-, di- or triethanolamine.

Bevorzugte Vertreter genügen den Formeln IIIa bis IIId,

        R1-CO-NH-(CH2)2-N(R3)-CH2CH2O-CH2-COOM     (IIIa)

        R'-CO-NH-(CH2)2-N(R3)-CH2CH2O-CH2CH2-COOM     (IIIb)

        R1-CO-NH-(CH2)2-N(R3)-CH2CH2O-CH2CH(OH)CH2-SO3M     (IIIc)

        R1-CO-NH-(CH2)2-N(R3)-CH2CH2O-CH2CH(OH)CH2-OPO3HM     (IIId)

in denen R1, R3 und M die gleiche Bedeutung wie in Formel (III) haben.
Preferred representatives satisfy the formulas IIIa to IIId,

R 1 -CO-NH- (CH 2 ) 2 -N (R 3 ) -CH 2 CH 2 O-CH 2 -COOM (IIIa)

R'-CO-NH- (CH 2 ) 2 -N (R 3 ) -CH 2 CH 2 O-CH 2 CH 2 -COOM (IIIb)

R 1 -CO-NH- (CH 2 ) 2 -N (R 3 ) -CH 2 CH 2 O-CH 2 CH (OH) CH 2 -SO 3 M (IIIc)

R 1 -CO-NH- (CH 2 ) 2 -N (R 3 ) -CH 2 CH 2 O-CH 2 CH (OH) CH 2 -OPO 3 HM (IIId)

in which R 1 , R 3 and M have the same meaning as in formula (III).

Beispielhafte Alkylamidoalkylamine sind die folgenden gemäß INCl benannten Verbindungen: Cocoamphodipropionic Acid, Cocobetainamido Amphopropionate, DEA-Cocoamphodipropionate, Disodium Caproamphodiacetate, Disodium Caproamphodipropionate, Disodium Capryloamphodiacetate, Disodium Capryloamphodipropionate, Disodium Cocoamphocarboxyethylhydroxypropylsulfonate, Disodium Cocoamphodiacetate, Disodium Cocoamphodipropionate, Disodium Isostearoamphodiacetate, Disodium Isostearoamphodipropionate, Disodium Laureth-5 Carboxyamphodiacetate, Disodium Lauroamphodiacetate, Disodium Lauroamphodipropionate, Disodium Oleoamphodipropionate, Disodium PPG-2-Isodeceth-7 Carboxyamphodiacetate, Disodium Stearoamphodiacetate, Disodium Tallowamphodiacetate, Disodium Wheatgermamphodiacetate, Lauroamphodipropionic Acid, Quaternium-85, Sodium Caproamphoacetate, Sodium Caproamphohydroxypropylsulfonate, Sodium Caproamphopropionate, Sodium Capryloamphoacetate, Sodium Capryloamphohydroxypropylsulfonate, Sodium Capryloamphopropionate, Sodium Cocoamphoacetate, Sodium Cocoamphohydroxypropylsulfonate, Sodium Cocoamphopropionate, Sodium Cornamphopropionate, Sodium Isostearoamphoacetate, Sodium Isostearoamphopropionate, Sodium Lauroamphoacetate, Sodium Lauroamphohydroxypropylsulfonate, Sodium Lauroampho PG-Acetate Phosphate, Sodium Lauroamphopropionate, Sodium Myristoamphoacetate, Sodium Oleoamphoacetate, Sodium Oleoamphohydroxypropylsulfonate, Sodium Oleoamphopropionate, Sodium Ricinoleoamphoacetate, Sodium Stearoamphoacetate, Sodium Stearoamphohydroxypropylsulfonate, Sodium Stearoamphopropionate, Sodium Tallamphopropionate, Sodium Tallowamphoacetate, Sodium Undecylenoamphoacetate, Sodium Undecylenoamphopropionate, Sodium Wheat Germamphoacetate und Trisodium Lauroampho PG-Acetate Chloride Phosphate. Vorzugsweise ist das Alkylamidoalkylamin ausgewählt aus der Gruppe umfassend Disodium Cocoamphodiacetate, Disodium Lauroamphodiacetate, Sodium Stearoamphoacetate, Sodium Cocoamphoacetate, Disodium Cocoamphodipropionate, Disodium Stearoamphodiacetate sowie Gemische derselben und insbesondere bevorzugt Disodium Cocoamphodiacetate (Natriumkokosamphodiacetat).Exemplary alkylamidoalkylamines are the following INCI named in accordance compounds: Cocoamphodipropionic Acid, Cocobetainamido amphopropionates, DEA-Cocoamphodipropionate, Disodium Caproamphodiacetate, Disodium Caproamphodipropionate, Disodium Capryloamphodiacetate, Disodium Capryloamphodipropionate, Disodium Cocoamphocarboxyethylhydroxypropylsulfonate, Disodium Cocoamphodiacetate, Disodium Cocoamphodipropionate, Disodium Isostearoamphodiacetate, Disodium Isostearoamphodipropionate, Disodium laureth 5 Carboxyamphodiacetate, Disodium Lauroamphodiacetate, Disodium Lauroamphodipropionate, Disodium Oleoamphodipropionate, Disodium PPG-2-Isodeceth-7 Carboxyamphodiacetate, Disodium Stearoamphodiacetate, Disodium Tallowamphodiacetate, Disodium Wheatgermamphodiacetate, Lauroamphodipropionic Acid, Quaternium-85, Sodium Caproamphoacetate, Sodium Caproamphohydroxypropylsulfonate, Sodium Caproamphopropionate, Sodium Capryloamphoacetate, Sodium Capryloamphohydroxypropylsulfonate, Sodium Capryl oamphopropionate, Sodium Cocoamphoacetate, Sodium Cocoamphohydroxypropylsulfonate, Sodium Cocoamphopropionate, Sodium Cornamphopropionate, Sodium Isostearoamphoacetate, Sodium Isostearoamphopropionate, Sodium lauroamphoacetate, sodium Lauroamphohydroxypropylsulfonate, Sodium Lauroampho PG-Acetate Phosphate, Sodium Lauroamphopropionate, Sodium Myristoamphoacetate, Sodium Oleoamphoacetate, Sodium Oleoamphohydroxypropylsulfonate, Sodium Oleoamphopropionate, Sodium Ricinoleoamphoacetate, Sodium Stearoamphoacetate, Sodium Stearoamphohydroxypropylsulfonate, Sodium Stearoamphopropionate, Sodium Tallamphopropionate, Sodium Tallowamphoacetate, Sodium Undecylenoamphoacetate, Sodium Undecylenoamphopropionate, Sodium Wheat Germamphoacetate and Trisodium Lauroampho PG-Acetate Chloride Phosphate. The alkylamidoalkylamine is preferably selected from the group consisting of disodium cocoamphodiacetate, disodium lauroamphodiacetate, sodium stearoamphoacetate, sodium cocoamphoacetate, disodium cocoamphodipropionate, disodium stearoamphodiacetate and mixtures thereof, and in particular preferably disodium cocoamphodiacetate (sodium cocoamphodiacetate).

Fettalkoholalkoxylatefatty alcohol

Als Tenside auf fettchemischer Basis können weiterhin Fettalkoholalkoxylate in erfindungsgemäßen Mitteln eingesetzt werden. Hierbei handelt es sich um C8-C18-Alkoholpolyglykolether, d.h. ethoxylierte und/oder propoxylierte Alkohole mit 8 bis 18 C-Atomen im Alkylteil und 2 bis 15 Ethylenoxid- (EO) und/oder Propylenoxideinheiten (PO). Besonders bevorzugt werden C8-18-Fettalkoholethoxylate mit 2 bis 10 EO eingesetzt, insbesondere C12-14 Fettalkoholethoxylate mit 2 bis 8 EO, beispielsweise C12-14 -Fettalkoholethoxylat mit 7 EO.As surfactants based on oleochemicals it is also possible to use fatty alcohol alkoxylates in agents according to the invention. These are C 8 -C 18 -alcohol polyglycol ethers, ie ethoxylated and / or propoxylated alcohols having 8 to 18 C atoms in the alkyl moiety and 2 to 15 ethylene oxide (EO) and / or propylene oxide units (PO). Particular preference is given to using C 8-18 -fatty alcohol ethoxylates having 2 to 10 EO, in particular C 12-14 fatty alcohol ethoxylates having 2 to 8 EO, for example C 12-14 -fatty alcohol ethoxylate with 7 EO.

Fettalkoholethersulfatefatty alcohol

Als Tenside auf fettchemischer Basis eignen sich weiterhin Fettalkoholethersulfate (C8-C18-Alkylpolyglykolethersulfate).Also suitable as surfactants based on oleochemicals are fatty alcohol ether sulfates (C 8 -C 18 -alkyl polyglycol ether sulfates).

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 (Fettalkohole). In der Regel entsteht aus n Molen Ethylenoxid und einem Mol Alkohol, abhängig von den Reaktionsbedingungen ein komplexes Gemisch von Additionsprodukten unterschiedlichen Ethoxylierungsgrades. Eine weitere Ausführungsform besteht im Einsatz von Gemischen der Alkylenoxide, bevorzugt des Gemisches von Ethylenoxid und Propylenoxid. Ganz besonders bevorzugt im Sinne der vorliegenden Erfindung sind niederethoxylierte Fettalkohole (0,5 bis 4 mol EO, bevorzugt 1 bis 2,5 mol EO). Ein besonders bevorzugtes Fettalkoholethersulfat ist beispielsweise C12-14-Fettalkoholethersulfat mit 2 EO.Fatty alcohol ether sulfates are products of sulfation reactions on alkoxylated alcohols. The person skilled in the art generally understands, under alkoxylated alcohols, the reaction products of alkylene oxide, preferably ethylene oxide, with alcohols, preferably in the context of the present invention, the longer-chain alcohols (fatty alcohols). As a rule, n moles of ethylene oxide and one mole of alcohol, depending on the reaction conditions, form a complex mixture of addition products of different degrees of ethoxylation. A further embodiment consists in the use of mixtures of the alkylene oxides, preferably of the mixture of ethylene oxide and propylene oxide. For the purposes of the present invention, very particular preference is given to lower ethoxylated fatty alcohols (0.5 to 4 mol of EO, preferably 1 to 2.5 mol of EO). A particularly preferred fatty alcohol ether sulfate is, for example, C 12-14 fatty alcohol ether sulfate with 2 EO.

Die anionischen Tenside werden vorzugsweise als Natriumsalze eingesetzt, können aber auch als andere Alkali- oder Erdalkalimetallsalze, beispielsweise Magnesiumsalze, sowie in Form von Ammonium- oder Mono-, Di-, Tri- bzw. Tetraalkylammoniumsalzen enthalten sein, im Falle der Sulfonate auch in Form ihrer korrespondierenden Säure, z.B. Dodecylbenzolsulfonsäure.The anionic surfactants are preferably used as sodium salts, but may also be present as other alkali metal or alkaline earth metal salts, for example magnesium salts, and in the form of ammonium or mono-, di-, tri- or tetraalkylammonium salts, in the case of the sulfonates also in the form their corresponding acid, eg dodecylbenzenesulfonic acid.

pH-Stellmittel/ AlkaliträgerpH adjuster / alkali carrier

Zur Regulierung des pH-Werts kann das erfindungsgemäße Mittel zudem Säuren oder Basen bzw. flüchtiges Alkali enthalten.To regulate the pH, the agent according to the invention may also contain acids or bases or volatile alkali.

Flüchtiges Alkali; BasenVolatile alkali; bases

Als flüchtiges Alkali werden Ammoniak und/oder Alkanolamine, die bis zu 9 C-Atome im Molekül enthalten können, verwendet. Als Alkanolamine werden die Ethanolamine bevorzugt und von diesen wiederum das Monoethanolamin. Der Gehalt an Ammoniak und/oder Alkanolamin beträgt vorzugsweise 0,01 bis 2 Gew.-%; besonders bevorzugt wird Ammoniak eingesetzt.
Daneben können die erfindungsgemäßen Reinigungsmittel auch geringe Mengen an Basen enthalten. Bevorzugte Basen stammen aus der Gruppe der Alkali- und Erdalkalimetallhydroxide und -carbonate, insbesondere der Alkalimetallhydroxide, von denen Kaliumhydroxid, Natriumhydroxid sowie Gemische derselben besonders bevorzugt sind.
The volatile alkali used is ammonia and / or alkanolamines, which may contain up to 9 C atoms in the molecule. As alkanolamines, the ethanolamines are preferred and of these in turn the monoethanolamine. The content of ammonia and / or alkanolamine is preferably 0.01 to 2 wt .-%; ammonia is particularly preferably used.
In addition, the cleaning agents according to the invention may also contain small amounts of bases. Preferred bases are selected from the group of alkali and alkaline earth metal hydroxides and carbonates, in particular the alkali metal hydroxides, of which potassium hydroxide, sodium hydroxide and mixtures thereof are particularly preferred.

Säurenacids

Alkalische Mittel können neben dem flüchtigen Alkali zusätzlich Carbonsäure enthalten, wobei das Äquivalentverhältnis von Amin und/oder Ammoniak zu Carbonsäure vorzugsweise zwischen 1 : 0,9 und 1 : 0,1 liegt. Geeignet sind Carbonsäuren mit bis zu 6 C-Atomen, wobei es sich um Mono-, Di-oder Polycarbonsäuren handeln kann. Je nach Äquivalentgewicht von Amin und Carbonsäure liegt der Gehalt an Carbonsäure vorzugweise zwischen 0,01 und 2,7 Gew.-%, insbesondere zwischen 0,01 und 0,9 Gew.-%. Beispiele geeigneter Carbonsäuren sind Essigsäure, Glykolsäure, Milchsäure, Citronensäure, Bernsteinsäure, Adipinsäure, Äpfelsäure, Weinsäure und Gluconsäure, von denen vorzugsweise Essigsäure, Citronensäure und Milchsäure verwendet werden. Besonders bevorzugt wird Citronensäure eingesetzt.Alkaline agents may additionally contain carboxylic acid in addition to the volatile alkali, wherein the equivalent ratio of amine and / or ammonia to carboxylic acid is preferably between 1: 0.9 and 1: 0.1. Suitable carboxylic acids having up to 6 carbon atoms, which may be mono-, di- or polycarboxylic acids. Depending on the equivalent weight of amine and carboxylic acid, the content of carboxylic acid is preferably between 0.01 and 2.7% by weight, in particular between 0.01 and 0.9% by weight. Examples of suitable carboxylic acids are acetic acid, glycolic acid, lactic acid, citric acid, succinic acid, adipic acid, malic acid, tartaric acid and gluconic acid, of which preferably acetic acid, citric acid and lactic acid are used. Citric acid is particularly preferably used.

Das erfindungsgemäße Mittel weist vorzugsweise einen pH-Wert zwischen 7 und 11,5 auf.The composition according to the invention preferably has a pH of between 7 and 11.5.

Ein bevorzugtes erfindungsgemäßes Reinigungsmittel enthält

  • 0.1 bis 15 Gew.-% Tallölseife,
  • 0,1 bis 12 Gew. % mindestens eines Tensids auf fettchemischer Basis,
  • 0,2 bis 15 % mindestens eines C1-C6-Alkohols sowie
  • 0,05 - 10 Gew. % eines Alkaliträgers,
wobei die Restalkalimenge nicht mehr als 5 % beträgt.A preferred cleaning agent according to the invention contains
  • 0.1 to 15% by weight tall oil soap,
  • 0.1 to 12% by weight of at least one surfactant based on oleochemical,
  • 0.2 to 15% of at least one C 1 -C 6 -alcohol and
  • 0.05-10% by weight of an alkali carrier,
the residual alkali amount is not more than 5%.

Weitere InhaltsstoffeOther ingredients

Neben den genannten kann das erfindungsgemäße Mittel weitere, üblicherweise in Reinigungsmitteln eingesetzte Inhaltsstoffe enthalten. Vorzugsweise sind diese ausgewählt aus der Gruppe umfassend Farbstoffe, Co-Tenside, Desinfektionsmittel, pH-Puffer, Verdicker, organische und anorganische Salze, weitere Lösemittel, vorzugsweise solche, die im allgemeinen als wohlriechend empfunden werden, optische Aufheller, Antioxidantien, Trübungsmittel, Hydrotrope, Abrasiva, Konservierungsmittel, Oxidationsmittel, Insektizide, Enzyme, probiotische Inhaltsstoffe, Hautschutz- und Hautpflegemittel, sowie Gemische derselben.In addition to those mentioned, the composition according to the invention may contain further ingredients usually used in cleaning agents. Preferably, these are selected from the group consisting of dyes, co-surfactants, disinfectants, pH buffers, thickeners, organic and inorganic salts, other solvents, preferably those which are generally perceived as fragrant, optical brighteners, antioxidants, opacifiers, hydrotropes, Abrasives, preservatives, oxidizing agents, insecticides, enzymes, probiotic ingredients, skin protection and skin care products, and mixtures thereof.

Co-TensideCosurfactants

Das erfindungsgemäße Mittel kann neben den genannten Inhaltsstoffen weitere oberflächenaktive Substanzen enthalten. Als oberflächenaktive Substanzen eignen sich für die erfindungsgemäßen Mittel Tenside aus den Klassen der anionischen, nichtionischen, kationischen und amphoteren Tenside. Vorzugsweise werden auch hier Tenside mit Anteilen aus nachwachsenden Rohstoffen eingesetzt.The agent according to the invention may contain, in addition to the ingredients mentioned, further surface-active substances. Suitable surface-active substances for the compositions according to the invention are surfactants from the classes of anionic, nonionic, cationic and amphoteric surfactants. Preferably, surfactants with proportions of renewable raw materials are also used here.

Als anionische Tenside eignen sich vorzugsweise C8-C20-Alkansulfonate, C8-C18-Monoalkylsulfate sowie Sulfobernsteinsäuremono- und -di-C8-C18-Alkylester. Weiterhin können auch C8-C18-α-Olefinsulfonate, sulfonierte C8-C18-Fettsäuren, C8-C22-Carbonsäureamidethersulfate, C8-C18-Alkylpolyglykolethercarboxylate, C8-C18-N-Acyltauride, C8-C18-N-Sarkosinate und C8-C18-Alkylisethionate bzw. deren Mischungen verwendet werden.
Die anionischen Tenside werden vorzugsweise als Natriumsalze eingesetzt, können aber auch als andere Alkali- oder Erdalkalimetallsalze, beispielsweise Magnesiumsalze, sowie in Form von Ammonium- oder Mono-, Di-, Tri- bzw. Tetraalkylammoniumsalzen enthalten sein, im Falle der Sulfonate auch in Form ihrer korrespondierenden Säure. Beispiele derartiger Tenside sind Natriumkokosalkylsulfat, Natrium-sec.-Alkansulfonat mit ca. 15 C-Atomen sowie Natriumdioctylsulfosuccinat.
In einer besonders bevorzugten Ausführungsform ist das erfindungsgemäße Mittel dagegen frei von linearen Alkylbenzolsulfonattensiden (LAS), die bislang in Reinigungsmitteln häufig als Aniontenside eingesetzt wurden.
Suitable anionic surfactants are preferably C 8 -C 20 -alkanesulfonates, C 8 -C 18 -monoalkyl sulfates and sulfosuccinic mono- and di-C 8 -C 18 -alkyl esters. Furthermore, C 8 -C 18 -α-olefinsulfonates, sulfonated C 8 -C 18 fatty acids, C 8 -C 22 -Carbonsäureamidethersulfate, C 8 -C 18 -Alkylpolyglykolethercarboxylate, C 8 -C 18 -N-Acyltauride, C 8 -C 18 -N-sarcosinates and C 8 -C 18 -alkyl isethionates or mixtures thereof.
The anionic surfactants are preferably used as sodium salts, but may also be present as other alkali or alkaline earth metal salts, for example magnesium salts, and in the form of ammonium or mono-, di-, tri- or tetraalkylammonium salts, in the case of the sulfonates also in the form their corresponding acid. Examples of such surfactants are sodium cocoalkyl sulfate, sodium sec-alkanesulfonate having about 15 carbon atoms and sodium dioctylsulfosuccinate.
In a particularly preferred embodiment, however, the agent according to the invention is free of linear alkylbenzenesulfonate surfactants (LAS), which have hitherto been used frequently in cleaning agents as anionic surfactants.

Als nichtionische Tenside sind vor allem C8-C18-Carbonsäurepolyglykolester mit 2 bis 15 EO, beispielsweise Talgfettsäure+6-EO-ester, ethoxylierte Fettsäureamide mit 12 bis 18 C-Atomen im Fettsäureteil und 2 bis 8 EO, etwa Laurinsäurediethanolamid, und langkettige Aminoxide mit 14 bis 20 C-Atomen wie das Kokosalkyldimethylaminoxid zu erwähnen.Particularly suitable nonionic surfactants are C 8 -C 18 -carboxylic acid polyglycol esters having 2 to 15 EO, for example tallow fatty acid + 6-EO esters, ethoxylated fatty acid amides having 12 to 18 C atoms in the fatty acid moiety and 2 to 8 EO, for example lauric acid diethanolamide, and long-chain ones Mention is made of amine oxides having 14 to 20 carbon atoms, such as the cocoalkyldimethylamine oxide.

Geeignete Amphotenside sind beispielsweise Betaine der Formel (Rii)(Riii)(Riv)N+CH2COO-, in der R" einen gegebenenfalls durch Heteroatome oder Heteroatomgruppen unterbrochenen Alkylrest mit 8 bis 25, vorzugsweise 10 bis 21 Kohlenstoffatomen und Riii sowie Riv gleichartige oder verschiedene Alkylreste mit 1 bis 3 Kohlenstoffatomen bedeuten, insbesondere C10-C18-Alkyl-dimethylcarboxymethylbetain und C11-C17-Alkylamidopropyl-dimethylcarboxymethylbetain.Suitable amphoteric surfactants are, for example, betaines of the formula (R ii ) (R iii ) (R v ) N + CH 2 COO - , in which R "is an alkyl radical optionally interrupted by hetero atoms or heteroatom groups having 8 to 25, preferably 10 to 21 carbon atoms and R iii and Ri v are identical or different alkyl radicals having 1 to 3 carbon atoms, in particular C 10 -C 18 -alkyl-dimethylcarboxymethylbetain and C 11 -C 17 -alkylamidopropyl-dimethylcarboxymethylbetain.

Geeignete Kationtenside sind u.a. die quartären Ammoniumverbindungen der Formel (Rv)(Rvi)(Rvii)(Rviii)N+ X-, in der Rv bis Rviii für vier gleich- oder verschiedenartige, insbesondere zwei lang- und zwei kurzkettige, Alkylreste und X- für ein Anion, insbesondere ein Halogenidion, stehen, beispielsweise Didecyl-dimethyl-ammoniumchlorid, Alkyl-benzyl-didecyl-ammoniumchlorid und deren Mischungen.Suitable cationic surfactants include the quaternary ammonium compounds of the formula (R v ) (R vi ) (R vii ) (R viii ) N + X - , in which R v to R viii for four identical or different, in particular two long and two short-chain, alkyl radicals and X - represent an anion, in particular a halide ion, for example, didecyl-dimethyl-ammonium chloride, alkyl-benzyl-didecyl-ammonium chloride and mixtures thereof.

Verdickerthickener

Es kann wünschenswert sein, die Viskosität des erfindungsgemäßen Mittels durch Zusatz eines Verdickungsmittels einzustellen Hierzu eignen sich alle üblicherweise in Wasch- und Reinigungsmitteln eingesetzten Viskositätsregulatoren, zu denen beispielsweise organische natürliche Verdickungsmittel (Agar-Agar, Carrageen, Tragant, Gummi arabicum, Alginate, Pektine, Polyosen, Guar-Mehl, Johannisbrotbaumkernmehl, Stärke, Dextrine, Gelatine, Casein), organische abgewandelte Naturstoffe (Carboxymethylcellulose und andere Celluloseether, Hydroxyethyl- und -propylcellulose und dergleichen, Kernmehlether), organische vollsynthetische Verdickungsmittel (Polyacryl- und Polymethacryl-Verbindungen, Vinylpolymere, Polycarbonsäuren, Polyether, Polyimine, Polyamide) und anorganische Verdickungsmittel (Polykieselsäuren, Tonmineralien wie Montmorillonite, Zeolithe, Kieselsäuren) zählen.
Vorzugsweise ist das erfindungsgemäße Mittel jedoch frei von Verdickern. Die Viskosität des erfindungsgemäßen Mittels beträgt vorzugsweise 0,4 bis 400 mPas (Brookfield LVDV 2+ mit small sample adapter, Spindel 31, 30 U/min, 20°C, unverdünntes Produkt).
It may be desirable to adjust the viscosity of the agent according to the invention by adding a thickener. All viscosity regulators commonly used in detergents and cleaning agents are suitable, for example organic natural thickeners (agar-agar, carrageenan, tragacanth, gum arabic, alginates, pectins, Polyols, guar gum, locust bean gum, starch, dextrins, gelatin, casein), organic modified natural products (carboxymethyl cellulose and other cellulose ethers, hydroxyethyl and propyl cellulose and the like, gum ethers), organic fully synthetic thickeners (polyacrylic and polymethacrylic compounds, vinyl polymers, Polycarboxylic acids, polyethers, polyimines, polyamides) and inorganic thickeners (polysilicic acids, clay minerals such as montmorillonites, zeolites, silicic acids).
Preferably, however, the agent according to the invention is free of thickeners. The viscosity of the composition according to the invention is preferably 0.4 to 400 mPas (Brookfield LVDV 2+ with small sample adapter, spindle 31, 30 rpm, 20 ° C., undiluted product).

antibakterielle Wirkstoffeantibacterial agents

Eine besondere Form der Reinigung stellen die Desinfektion und die Sanitation dar. In einer entsprechenden besonderen Ausführungsform der Erfindung enthält das Reinigungsmittel daher einen oder mehrere antimikrobielle Wirkstoffe, vorzugsweise in einer Menge von 0,01 bis 2 Gew.%, vorzugsweise 0,02 bis 0,9 Gew.-%, insbesondere 0,05 bis 0,5 Gew.-%, besonders bevorzugt 0,1 bis 0,4 Gew.-%, äußerst bevorzugt 0,3 Gew.-%.
Die Begriffe Desinfektion, Sanitation, antimikrobielle Wirkung und antimikrobieller Wirkstoff haben im Rahmen der erfindungsgemäßen Lehre die fachübliche Bedeutung, die beispielsweise von K. H. Wallhäußer in "Praxis der Sterilisation, Desinfektion - Konservierung : Keimidentifizierung - Betriebshygiene" (5. Aufl. - Stuttgart ; New York : Thieme, 1995 ) wiedergegeben wird. Während Desinfektion im engeren Sinne der medizinischen Praxis die Abtötung von - theoretisch allen - Infektionskeimen bedeutet, ist unter Sanitation die möglichst weitgehende Elimierung aller - auch der für den Menschen normalerweise unschädlichen saprophytischen - Keime zu verstehen. Hierbei ist das Ausmaß der Desinfektion bzw. Sanitation von der antimikrobiellen Wirkung des angewendeten Mittels abhängig, die mit abnehmendem Gehalt an antimikrobiellem Wirkstoff bzw. zunehmender Verdünnung des Mittels zur Anwendung abnimmt.
Erfindungsgemäß geeignet sind beispielsweise antimikrobielle Wirkstoffe aus den Gruppen der Alkohole, Aldehyde, antimikrobiellen Säuren bzw. deren Salze, Carbonsäureester, Säureamide, Phenole, Phenolderivate, Diphenyle, Diphenylalkane, Harnstoffderivate, Sauerstoff-, Stickstoff-Acetale sowie -Formale, Benzamidine, Isothiazole und deren Derivate wie Isothiazoline und Isothiazolinone, Phthalimidderivate, Pyridinderivate, antimikrobiellen oberflächenaktiven Verbindungen, Guanidine, antimikrobiellen amphoteren Verbindungen, Chinoline, 1,2-Dibrom-2,4-dicyanobutan, lodo-2-propynyl-butyl-carbamat, Iod, Iodophore und Peroxide. Bevorzugte antimikrobielle Wirkstoffe werden vorzugsweise ausgewählt aus der Gruppe umfassend Ethanol, n-Propanol, i-Propanol, 1,3-Butandiol, Phenoxyethanol, 1,2-Propylenglykol, Glycerin, Undecylensäure, Zitronensäure, Milchsäure, Benzoeesäure, Salicylsäure, Thymol, 2-Benzyl-4-chlorphenol, 2,2'-Methylen-bis-(6-brom-4-chlorphenol), 2,4,4'-Trichlor-2'-hydroxydiphenylether, N-(4-Chlorphenyl)-N-(3,4-dichlorphenyl)-harnstoff, N,N'-(1,10-decandiyldi-1-pyridinyl-4-yliden)-bis-(1-octanamin)-dihydrochlorid, N,N'-Bis-(4-Chlorphenyl)-3,12-diimino-2,4,11,13-tetraazatetradecandiimidamid, antimikrobielle quaternäre oberflächenaktive Verbindungen, Guanidine. Bevorzugte antimikrobiell wirkende oberflächenaktive quaternäre Verbindungen enthalten eine Ammonium-, Sulfonium-, Phosphonium-, Jodonium- oder Arsoniumgruppe, wie sie beispielsweise K. H. Wallhäußer in "Praxis der Sterilisation, Desinfektion - Konservierung : Keimidentifizierung - Betriebshygiene" (5. Aufl. - Stuttgart ; New York : Thieme, 1995 ) beschreibt. Weiterhin können auch antimikrobiell wirksame ätherische Öle eingesetzt werden, die gleichzeitig für eine Beduftung des Reinigungsmittels sorgen. Besonders bevorzugte antimikrobielle Wirkstoffe sind jedoch ausgewählt aus der Gruppe umfassend Salicylsäure, quaternäre Tenside, insbesondere Benzalkoniumchlorid, Peroxo-Verbindungen, insbesondere Wasserstoffperoxid, Alkalimetallhypochlorit sowie Gemische derselben.
Disinfection and sanitation constitute a particular form of purification. In a corresponding particular embodiment of the invention, the cleaning agent therefore contains one or more antimicrobial agents, preferably in an amount of 0.01 to 2% by weight, preferably 0.02 to 0 , 9 wt .-%, in particular 0.05 to 0.5 wt .-%, particularly preferably 0.1 to 0.4 wt .-%, most preferably 0.3 wt .-%.
The terms disinfection, sanitation, antimicrobial action and antimicrobial agent have the usual meaning in the context of the teaching of the invention, the example of KH Wallhäußer in "Practice of Sterilization, Disinfection - Conservation: Germ Identification - Plant Hygiene" (5th edition - Stuttgart, New York: Thieme, 1995 ) is reproduced. While disinfection in the narrower sense of the medical practice means the killing of - in theory all - infectious germs, sanitation is to be understood as the greatest possible elimination of all - including the saprophytic - normally harmless to humans saprophytic - germs. Here, the extent of disinfection or sanitation depends on the antimicrobial effect of the applied agent, which decreases with decreasing content of antimicrobial agent or increasing dilution of the agent for use.
For example, antimicrobial agents from the groups of alcohols, aldehydes, antimicrobial acids or their salts, carboxylic esters, acid amides, phenols, phenol derivatives, diphenyls, diphenylalkanes, urea derivatives, oxygen, nitrogen acetals and formals, benzamidines, isothiazoles and their derivatives are suitable according to the invention Derivatives such as isothiazolines and isothiazolinones, phthalimide derivatives, pyridine derivatives, antimicrobial surface-active compounds, guanidines, antimicrobial amphoteric compounds, quinolines, 1,2-dibromo-2,4-dicyanobutane, iodo-2-propynyl-butyl-carbamate, iodine, iodophores and peroxides. Preferred antimicrobial agents are preferably selected from the group comprising ethanol, n-propanol, i-propanol, 1,3-butanediol, phenoxyethanol, 1,2-propylene glycol, glycerol, undecylenic acid, citric acid, lactic acid, benzoic acid, salicylic acid, thymol, 2- Benzyl 4-chlorophenol, 2,2'-methylenebis (6-bromo-4-chlorophenol), 2,4,4'-trichloro-2'-hydroxydiphenyl ether, N- (4-chlorophenyl) -N- ( 3,4-dichlorophenyl) urea, N, N '- (1,10-decanediyldi-1-pyridinyl-4-ylidene) bis (1-octanamine) dihydrochloride, N, N'-bis (4- Chlorophenyl) -3,12-diimino-2,4,11,13-tetraazatetradecandiimidamide, antimicrobial quaternary surface active compounds, guanidines. Preferred antimicrobial surface active quaternary compounds contain an ammonium, sulfonium, phosphonium, iodonium or arsonium group, as for example KH Wallhäußer in "Practice of Sterilization, Disinfection - Conservation: Germ Identification - Plant Hygiene" (5th edition - Stuttgart, New York: Thieme, 1995 ) describes. Furthermore, antimicrobially effective essential oils can be used, which at the same time provide for a scenting of the cleaning agent. However, particularly preferred antimicrobial agents are selected from the group comprising salicylic acid, quaternary surfactants, in particular benzalkonium chloride, peroxo compounds, in particular hydrogen peroxide, alkali metal hypochlorite and mixtures thereof.

Konservierungsstoffepreservatives

Konservierungsmittel können gleichfalls in erfindungsgemäßen Mitteln enthalten sein. Als solche können im wesentlichen die bei den antimikrobiellen Wirkstoffen genannten Stoffe eingesetzt werden.Preservatives may also be included in compositions of the invention. As such, essentially the substances mentioned in the antimicrobial agents can be used.

Hautschutz- und HautpflegemittelSkin protection and skin care products

Das erfindungsgemäße Mittel kann zudem Hautschutz-und Hautpflegemittel enthalten. Als solche eignen sich alle bekannten pflegenden Wirkstoffe, zu denen beispielsweise Bisabolol, Allantoin, Vitamine wie Panthenol, natürliche Öle wie Mandelöl, Pflanzenextrakte etwa aus der Ringelblume, Aloe Vera, pflegende Wachsdispersionen, pflegende Polymere und weitere in kosmetischen Mitteln eingesetzte Pflege- und Konditioniermittel sowie Gemische zählen.The composition according to the invention may additionally contain skin protection and skin care agents. As such are all known care agents, including bisabolol, allantoin, vitamins such as panthenol, natural oils such as almond oil, plant extracts such as marigold, aloe vera, nourishing wax dispersions, nourishing polymers and other used in cosmetic care and conditioning agents and Count mixtures.

Das Mittel kann in einer bevorzugten Ausführungsform auf die zu reinigende Oberfläche aufgesprüht bzw. in Form eines Schaums aufgetragen werden. Hierzu eignet sich in besonderer Weise ein manuell aktivierter Sprühspender, insbesondere ausgewählt aus der Gruppe, umfassend Aerosolsprühspender, selbst Druck aufbauende Sprühspender, Pumpsprühspender und Triggersprühspender, insbesondere Pumpsprühspender und Triggersprühspender mit einem Behälter aus Polyethylen, Polypropylen oder Polyethylenterephthalat. Solche Triggerflaschen werden beispielsweise von der Firma Afa-Polytec angeboten. Der Sprühkopf ist vorzugsweise mit einer Schaumdüse ausgestattet. Neben Triggerflaschen eignen sich auch Pumpschaumspender, wie sie beispielsweise von der Firma Airspray oder auch der Daiwa Can Company angeboten werden. Daneben kann das Mittel auch unter Zusatz eines geeigneten Treibmittels (z.B. n-Butan, ein Propan/Butan-Gemisch, Kohlendioxid, Stickstoff oder ein CO2/N2-Gemisch) in eine entsprechende Aerosolsprühflasche gefüllt werden. Ein solcher Sprühspender ist jedoch weniger bevorzugt.In a preferred embodiment, the agent can be sprayed onto the surface to be cleaned or applied in the form of a foam. Particularly suitable for this purpose is a manually activated spray dispenser, in particular selected from the group comprising aerosol spray dispensers, pressure-building spray dispensers, pump spray dispensers and trigger spray dispensers, in particular pump spray dispensers and trigger spray dispensers with a container made of polyethylene, polypropylene or polyethylene terephthalate. Such trigger bottles are offered for example by the company Afa-Polytec. The spray head is preferably equipped with a foam nozzle. In addition to trigger bottles, pump foam dispensers, such as those offered by the company Airspray or the Daiwa Can Company, are also suitable. In addition, the agent can also be added with the addition of a suitable propellant (eg n-butane, a propane / butane mixture, carbon dioxide, nitrogen, or a CO 2 / N 2 mixture) are charged into a corresponding Aerosolsprühflasche. However, such a spray dispenser is less preferred.

Ein weiterer Erfindungsgegenstand ist dementsprechend ein Erzeugnis aus einem erfindungsgemäßen Reinigungsmittel und einem Sprühspender, insbesondere aus einem erfindungsgemäßen Reinigungsmittel und einer Triggerflasche mit Schaumdüse.A further subject of the invention is accordingly a product comprising a cleaning agent according to the invention and a spray dispenser, in particular a cleaning agent according to the invention and a trigger bottle with a foam nozzle.

Die erfindungsgemäßen Mittel werden vorzugsweise zur Reinigung harter Oberflächen verwendet. Ein weiterer Erfindungsgegenstand ist daher die Verwendung eines erfindungsgemäßen Reinigungsmittels zur Reinigung harter Oberflächen. Harte Oberflächen im Sinne dieser Anmeldung sind dabei Fenster, Spiegel und weitere Glasoberflächen, Oberflächen aus Keramik, Kunststoff, Metall oder auch Holz sowie lackiertes Holz, die sich in Haushalt und Gewerbe finden, etwa Badkeramik, Küchenoberflächen oder Fußböden. Dabei wird das Reinigungsmittel vor der Anwendung mit Wasser verdünnt oder aber, insbesondere mittels eines Sprühspenders, unverdünnt aufgetragen. In einem Verfahren zur Reinigung harter Oberflächen wird daher das erfindungsgemäße Reinigungsmittel in einem Verfahrensschritt auf die zu reinigende Oberfläche aufgetragen.The agents according to the invention are preferably used for cleaning hard surfaces. Another subject of the invention is therefore the use of a cleaning agent according to the invention for cleaning hard surfaces. Hard surfaces in the context of this application are windows, mirrors and other glass surfaces, surfaces made of ceramic, plastic, metal or wood and lacquered wood, which are found in household and commercial, such as bathroom ceramics, kitchen surfaces or floors. The detergent is diluted before use with water or, in particular by means of a spray dispenser, applied undiluted. In a method for cleaning hard surfaces, therefore, the cleaning agent according to the invention is applied in one process step to the surface to be cleaned.

In einer weiteren bevorzugten Ausführungsform werden die erfindungsgemäßen Mittel zur Fleckentfernung und/oder zur Fleckenvorbehandlung auf Textilien eingesetzt. Hierbei eignen sie sich insbesondere zur Behandlung fetthaltiger Flecken. Ein weiterer Erfindungsgegenstand ist dementsprechend die Verwendung eines erfindungsgemäßen Reinigungsmittels zur Fleckentfernung und/oder zur Fleckenvorbehandlung auf Textilien, insbesondere bei fetthaltigen Flecken.In a further preferred embodiment, the agents according to the invention are used for stain removal and / or for spot pretreatment on textiles. Here they are particularly suitable for the treatment of fatty stains. A further subject of the invention is accordingly the use of a cleaning agent according to the invention for stain removal and / or for spot pretreatment on textiles, in particular for greasy stains.

Ausführungsbeispieleembodiments

Es wurden erfindungsgemäße Beispiele E1 bis E3 sowie ein nicht erfindungsgemäßes Vergleichsbeispiel V1 formuliert. Die Zusammensetzungen sind der nachfolgenden Tabelle 1 zu entnehmen. Die Mengenangaben sind dabei in Gew.-% Aktivstoff. Tabelle 1: E1 E2 E3 V1 Decylglycosid -- -- 2,0 2,0 C12-14-Fettalkohol mit 7 EO -- 2,0 -- 3,0 C12-14-Fettalkoholethersulfat 2 EO, Na-Salz -- -- 2,0 -- Tallölfettsäure C18-22, ungesättigt, Na-Salz 6,0 6,0 3,0 -- Fettsäure C12-18, Na-Salz -- -- -- 2,0 Cocoamphodiacetat, 2Na-Salz 3,0 2,0 1,0 -- Zitronensäure, monohydrat -- 0,5 -- 0,5 Propanol-2 9,0 6,0 -- -- Ethanol -- -- 8,0 3,0 Kalilauge 1,0 1,0 1,0 -- Natronlauge 0,6 0,6 0,6 0,6 Natriumcarbonat -- -- -- 2 Parfümöl ("Pine" von Givaudan) -- -- -- 0,4 Farbstoff -- -- 0,002 0,002 Wasser Ad 100 Ad 100 Ad 100 Ad 100 pH 9,0 9,0 9,0 9,0

  • Decylglycosid = APG 220 UPW, Cognis
  • C12-14-Fettalkohol mit 7 EO = Dehydol LT 7, Cognis
  • C12-14-Fettalkoholethersulfat 2 EO, Na-Salz = Texapon N70, Cognis
  • Tallölfettsäure C18-22, ungesättigt, Na-Salz = gebildet durch Verseifung aus Sylvatal 10 VS (destilliertes Tallöl bzw. Kiefernöl), Arizona Chemical
  • Fettsäure C12-18, Na-Salz = Edenor K12-18, Cognis
  • Cocoamphodiacetat, 2Na-Salz = Dehyton PS, Cognis
Inventive examples E1 to E3 and a comparative example C1 not according to the invention were formulated. The compositions are shown in Table 1 below. The quantities are in wt .-% active. Table 1: E1 E2 E3 V1 decyl - - 2.0 2.0 C 12-14 fatty alcohol with 7 EO - 2.0 - 3.0 C 12-14 fatty alcohol ether sulfate 2 EO, Na salt - - 2.0 - Tall oil fatty acid C18-22, unsaturated, Na salt 6.0 6.0 3.0 - Fatty acid C12-18, Na salt - - - 2.0 Cocoamphodiacetate, 2Na salt 3.0 2.0 1.0 - Citric acid, monohydrate - 0.5 - 0.5 2-propanol 9.0 6.0 - - ethanol - - 8.0 3.0 potassium hydroxide 1.0 1.0 1.0 - caustic soda 0.6 0.6 0.6 0.6 sodium - - - 2 Perfume oil ("Pine" by Givaudan) - - - 0.4 dye - - 0,002 0,002 water Ad 100 Ad 100 Ad 100 Ad 100 pH 9.0 9.0 9.0 9.0
  • Decyl glycoside = APG 220 UPW, Cognis
  • C 12-14 fatty alcohol with 7 EO = Dehydol LT 7, Cognis
  • C 12-14 fatty alcohol ether sulfate 2 EO, Na salt = Texapon N70, Cognis
  • Tall oil fatty acid C18-22, unsaturated, Na salt = formed by saponification from Sylvatal 10 VS (distilled tall oil or pine oil), Arizona Chemical
  • Fatty acid C12-18, Na salt = Edenor K12-18, Cognis
  • Cocoamphodiacetate, 2Na salt = Dehyton PS, Cognis

Sowohl die erfindungsgemäßen Reinigungsmittel als auch die Vergleichsrezeptur wurden gemäß der IKW-Empfehlung zur Bewertung von Allzweckreinigern hinsichtlich ihres Reinigungsvermögens geprüft. Alle wiesen eine gute Reinigungsleistung auf.Both the detergents according to the invention and the comparative formulation were tested according to the IKW recommendation for the evaluation of all-purpose cleaners in terms of their cleaning power. All had a good cleaning performance.

Zudem wurde der Duft der Formulierungen durch ein Expertenpanel von fünf geschulten Personen sowohl am konzentrierten Produkt als auch in Anwendungskonzentration abgerochen und der Dufteindruck auf einer Notenskala von 1 (sehr gut) bis 7 (unangenehm) bewertet.In addition, the fragrance of the formulations was scented by an expert panel of five trained persons on the concentrated product as well as in the application concentration and the fragrance impression was rated on a grading scale from 1 (very good) to 7 (unpleasant).

Das Ergebnis ist in der nachfolgenden Tabelle wiedergegeben: Bewertung Produkteigenschaften E1 E2 E3 V1 Reinigungsleistung IKW-Test +++ ++ ++ +++ Rückstandsverhalten ++ +++ +++ ++ Spannungsrißverhalten ++ + ++ + Dufteindruck am Produkt 2,3 3,2 3,1 3,3 Dufteindruck in Anwendungsverdünnung 2,5 2,9 2,7 2,9 The result is shown in the following table: Review product features E1 E2 E3 V1 Cleaning performance IKW test +++ ++ ++ +++ residue behavior ++ +++ +++ ++ Stress cracking ++ + ++ + Fragrance impression on the product 2.3 3.2 3.1 3.3 Fragrance impression in application dilution 2.5 2.9 2.7 2.9

Es zeigte sich, dass die erfindungsgemäß parfümfreien Rezepturen einen gleich guten oder sogar positiveren Dufteindruck hinterließen als die parfümhaltige Vergleichsformulierung.It was found that the perfume-free formulations according to the invention left an equally good or even more positive scent impression than the perfume-containing comparative formulation.

Claims (13)

  1. An unscented aqueous cleaning agent for hard surfaces and textiles, characterized in that said cleaning agent contains from 0.1 to 15 wt.% tall oil soap, at least one C1-C6 alcohol, and from 0.1 to 12 wt.% of at least one surfactant based on fatty chemicals, the at least one surfactant based on fatty chemicals being selected from the group comprising alkyl polyglycosides, fatty alcohol alkoxylates, alkyl amido alkylamines, fatty alcohol ether sulfates and mixtures thereof.
  2. The cleaning agent according to claim 1, characterized in that said cleaning agent further contains a pH adjustment agent.
  3. The cleaning agent according to one of claims 1 and 2, characterized in that said cleaning agent further contains one or more common cleaning agent ingredients, preferably selected from the group comprising dyes, cosurfactants, disinfectants, pH buffers, thickeners, organic and inorganic salts, additional solvents, optical brighteners, antioxidants, opacifying agents, hydrotropic substances, abrasives, preservatives, oxidizing agents, insecticides, enzymes, probiotic ingredients, skin-protection and skincare agents, and mixtures thereof.
  4. The cleaning agent according to one of the preceding claims, characterized in that said cleaning agent has a pH of between 7 and 11.5.
  5. The cleaning agent according to one of the preceding claims, characterized in that said cleaning agent contains
    from 0.1 to 15 wt.% tall oil soap,
    from 0.1 to 12 wt.% of at least one surfactant based on fatty chemicals,
    from 0.2 to 15 % of at least one C1-C6 alcohol, and
    from 0.05 to 10 wt.% of an alkali carrier,
    the residual alkali amount not being more than 5 %.
  6. The cleaning agent according to one of the preceding claims, characterized in that the at least one fatty chemical surfactant is an alkyl polyglycoside, preferably decyl glycoside.
  7. The cleaning agent according to one of claims 1 to 5, characterized in that the at least one fatty chemical surfactant is an alkyl amido alkylamine, preferably cocoamphodiacetate.
  8. The cleaning agent according to one of claims 1 to 5, characterized in that the at least one fatty chemical surfactant is a fatty alcohol alkoxylate, preferably a fatty alcohol ethoxylate, particularly preferably a C12-14 fatty alcohol ethoxylate having from 2 to 8 ethylene oxide units.
  9. The cleaning agent according to one of claims 1 to 5, characterized in that the at least one fatty chemical surfactant is a fatty alcohol ether sulfate, preferably a C12-14 fatty alcohol ether sulfate having 2 ethylene oxide units.
  10. A product consisting of a cleaning agent according to one of the preceding claims and a spray dispenser, in particular consisting of a cleaning agent according to one of the preceding claims and a spray dispenser comprising a foam nozzle.
  11. The use of a cleaning agent according to one of claims 1 to 9 for cleaning hard surfaces.
  12. A method for cleaning hard surfaces, characterized in that the cleaning agent according to one of claims 1 to 9 is applied to the surface to be cleaned in one method step.
  13. The use of a cleaning agent according to one of claims 1 to 9 for removing stains and/or pre-treating stains on textiles, in particular greasy stains.
EP10747460.3A 2009-09-22 2010-08-30 Unperfumed cleaning agent Not-in-force EP2480646B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE200910029681 DE102009029681A1 (en) 2009-09-22 2009-09-22 Perfume-free cleaner
PCT/EP2010/062626 WO2011036032A1 (en) 2009-09-22 2010-08-30 Unperfumed cleaning agent

Publications (2)

Publication Number Publication Date
EP2480646A1 EP2480646A1 (en) 2012-08-01
EP2480646B1 true EP2480646B1 (en) 2016-10-05

Family

ID=43064665

Family Applications (1)

Application Number Title Priority Date Filing Date
EP10747460.3A Not-in-force EP2480646B1 (en) 2009-09-22 2010-08-30 Unperfumed cleaning agent

Country Status (3)

Country Link
EP (1) EP2480646B1 (en)
DE (1) DE102009029681A1 (en)
WO (1) WO2011036032A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR3109884B1 (en) * 2020-05-06 2022-04-15 Laboratoires Lea Eco-responsible detergent composition, its use and its impact on skin and ecological ecosystems

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2901433A (en) * 1953-07-17 1959-08-25 Pennsalt Chemicals Corp Cleaning composition
US3360471A (en) * 1963-04-18 1967-12-26 Sterling Drug Inc Biodegradable cleaning compound
SE345479B (en) * 1969-01-31 1972-05-29 Krueppelman J Med Fa Nordiska
US4477361A (en) * 1983-02-22 1984-10-16 Sperti Drug Products, Inc. Antifungal-antibacterial detergents containing cinnamic compounds
FR2640637A1 (en) * 1988-12-19 1990-06-22 Derives Resiniques Terpenique LIQUID CLEANER FOR SOLID SURFACES BASED ON TERPENIC DERIVATIVES AND METHOD FOR MANUFACTURING THE SAME
US5080831A (en) * 1989-06-29 1992-01-14 Buckeye International, Inc. Aqueous cleaner/degreaser compositions
US7396808B1 (en) 2007-06-20 2008-07-08 The Clorox Company Natural cleaning compositions

Also Published As

Publication number Publication date
DE102009029681A1 (en) 2011-03-24
WO2011036032A1 (en) 2011-03-31
EP2480646A1 (en) 2012-08-01

Similar Documents

Publication Publication Date Title
DE60032756T2 (en) REFRACTORY CLEANER COMPOSITIONS
AT394572B (en) STRONG FOAMING, LIQUID FINE CLEANING AGENT BASED ON NON-ionic surfactants, AND METHOD FOR THE PRODUCTION THEREOF
EP1750567B1 (en) Kit consisting of a sponge and a detergent
WO2000065007A2 (en) Cleaning agents for hard surfaces
EP1167499A1 (en) Liquid detergent compositions comprising mixed hydroxyethers
DE19906481A1 (en) Gel-shaped detergent for flush toilets
WO2000065011A1 (en) Cleaning agents for hard surfaces
DE19910788A1 (en) Gel-shaped detergent for flush toilets
WO2012084151A1 (en) Compositions containing secondary paraffin sulfonate and alcohol alkoxylate
DE69636598T2 (en) Sprayable composition and its use for disinfecting surfaces
DE102004063765A1 (en) Foam-reinforced cleaner
EP3744819A1 (en) Composition with alkoxylated fatty acids
EP2480646B1 (en) Unperfumed cleaning agent
WO2000065010A1 (en) Cleaning agent for hard surfaces
EP1075502B1 (en) Dishwashing detergent with an antibacterial effect
DE102005013132A1 (en) Skin-friendly detergent mixtures
DE102005019658A1 (en) Aqueous disinfectant, useful for cleaning and disinfecting hard surfaces, comprises combination of benzalkonium chloride, phenoxyethanol and aminotrimethylenephosphonic acid
DE69633113T2 (en) Detergent compositions
DE10131721C1 (en) Quickly soluble cleaning gel
EP0925351B1 (en) Agent for cleaning hard surfaces
DE102007005942A1 (en) Hand dishwashing detergent with native surfactant combination
DE60210336T2 (en) BEAUTIFUL CLEANING LIQUIDS WITH PRESERVATION SYSTEM
WO2000065012A1 (en) Cleaning agents for hard surfaces
WO1999010458A1 (en) Aqueous agents for cleaning hard surfaces
WO2000065013A1 (en) Cleaning agents for hard surfaces

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20120124

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20150901

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

RIC1 Information provided on ipc code assigned before grant

Ipc: C11D 1/90 20060101ALI20160510BHEP

Ipc: C11D 10/06 20060101ALI20160510BHEP

Ipc: C11D 3/20 20060101AFI20160510BHEP

Ipc: C11D 15/04 20060101ALI20160510BHEP

Ipc: C11D 9/26 20060101ALI20160510BHEP

Ipc: C11D 1/66 20060101ALI20160510BHEP

Ipc: C11D 1/72 20060101ALI20160510BHEP

Ipc: C11D 10/04 20060101ALI20160510BHEP

INTG Intention to grant announced

Effective date: 20160603

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

Free format text: NOT ENGLISH

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 834676

Country of ref document: AT

Kind code of ref document: T

Effective date: 20161015

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

Free format text: LANGUAGE OF EP DOCUMENT: GERMAN

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 502010012514

Country of ref document: DE

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20161005

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170105

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170106

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170206

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170205

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 502010012514

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170105

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

26N No opposition filed

Effective date: 20170706

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20170822

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20170830

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170831

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170831

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20180430

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20170831

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170830

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170830

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170830

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170831

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170831

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

REG Reference to a national code

Ref country code: AT

Ref legal event code: MM01

Ref document number: 834676

Country of ref document: AT

Kind code of ref document: T

Effective date: 20170830

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170830

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 502010012514

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20100830

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190301

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20161005

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161005