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WO2010142480A1 - Odor-imparting detergent, cleaning or care product - Google Patents

Odor-imparting detergent, cleaning or care product Download PDF

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Publication number
WO2010142480A1
WO2010142480A1 PCT/EP2010/054918 EP2010054918W WO2010142480A1 WO 2010142480 A1 WO2010142480 A1 WO 2010142480A1 EP 2010054918 W EP2010054918 W EP 2010054918W WO 2010142480 A1 WO2010142480 A1 WO 2010142480A1
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WO
WIPO (PCT)
Prior art keywords
methyl
cleaning
dimethyl
weight
washing
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.)
Ceased
Application number
PCT/EP2010/054918
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German (de)
French (fr)
Inventor
Ursula Huchel
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Henkel AG and Co KGaA
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Henkel AG and Co KGaA
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Publication of WO2010142480A1 publication Critical patent/WO2010142480A1/en
Anticipated expiration legal-status Critical
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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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/50Perfumes
    • C11D3/502Protected perfumes
    • 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2072Aldehydes-ketones
    • 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/30Amines; Substituted amines ; Quaternized amines

Definitions

  • the present invention relates to a washing, cleaning or care agent containing ethylenediamines and / or propylenediamines. It further relates to a textile cleaning or conditioning method in which the textile to be cleaned is subjected to a textile washing using an appropriate washing, cleaning or care agent. It relates to the use of such an agent for cleaning and / or conditioning of textile fabrics, in particular in an automatic washing machine. It relates to the use of ethylenediamine and / or propylenediamine to extend the fragrance effect of the washing, cleaning or care product as well as to achieve a long-lasting fresh scent when using the washing, cleaning or care product.
  • washing, cleaning or care products the consumer not only pursues the goal of washing, cleaning or caring for the objects to be treated, but also desires that the treated objects, e.g. Textiles, like to smell good after washing. For this reason in particular, most commercially available washing, cleaning or care products contain fragrances.
  • the object of the present invention was therefore to provide washing, cleaning or care products which show improved fragrance intensity during use, in particular in connection with textile treatment.
  • the washing, cleaning or care agents according to the invention exhibit an improved fragrance intensity during use, in particular in connection with the textile treatment.
  • a laundry treatment agent according to the invention such as detergents and fabric softeners
  • an improved fragrance intensity of the treated laundry could be found. This applies to both wet and especially dry laundry.
  • a better durability of the scent impression was found, ie the desired scent impression lasted longer.
  • corresponding products have a particularly good storage stability.
  • the compositions according to the invention make it possible to reduce the total amount of perfume which is contained on average, and nevertheless to achieve odor advantages on the laundered textiles, in particular with regard to the sensation of freshness.
  • an agent according to the invention is characterized in that component (a) and component (b) are added separately to the washing, cleaning or care agent matrix.
  • component (a) and component (b) are added separately to the washing, cleaning or care agent matrix.
  • particularly advantageous scent intensities in the sense of the invention are made possible. It is e.g. According to the invention possible to introduce the component (a) with the rest of perfuming in the product and to introduce the component (b) in a separate step. Furthermore, it is also possible according to the invention to introduce components (a) and (b) into the product in a single step, e.g. together with the remainder of the perfume, provided that components (a) and (b) are separate when added, e.g. as separate components of a perfume oil.
  • fragrance aldehydes it is possible to use all customary fragrant aldehydes which are typically used to produce a pleasant scent sensation.
  • Suitable fragrance aldehydes are known to the person skilled in the art.
  • Suitable fragrance aldehydes may be any aldehydes, especially those which impart a desired fresh scent or sensation of freshness. Because this is particularly desirable according to the invention, especially with a view to a particularly intense and long-lasting feeling of freshness. It may be individual aldehydes or aldehyde mixtures.
  • the fragrance aldehydes may in particular have an aliphatic, cycloaliphatic, aromatic, ethylenically unsaturated structure or a combination of these structures. There may also be other heteroatoms or polycyclic structures.
  • a fragrance aldehyde selected from Adoxal, Anisaldehyd, Cymal, Ethylvanillin, Florhydral, Helional, Heliotropin, Hydroxycitronellal, Koavon, Lauraldehyd, Lyral, Methylnonylacetaldehyd, PT Bucinal, Phenylacetaldehyd, Undecylenaldehyd, Vanillin, 2,6,10-trimethyl-9-undecenal, 3-dodecene-1-al, alpha-n-amyl-cinnamic aldehyde, 4-methoxybenzaldehyde, benzaldehyde, 3- (4-tert-butylphenyl) -propanal, 2-methyl-3- (para-methoxyphenyl) propanal, 2-methyl-4- (2,6,6-t)
  • fragrance ketones in addition to the fragrance aldehyde.
  • a preferred embodiment of the invention is therefore present if in addition at least one fragrance ketone is used, in particular selected from buccoxime; iso-jasmone; Methyl-beta-naphthyl ketone; musk indanone; Tonalid / Musk plus; alpha damascone, beta Damascone, delta-damascon, iso-damascon, damascenon, damarose, methyldihydrojasmonate, menthone, carvone, camphor, fenchone, alpha-ionone, beta-ionone, gamma-methyl called lonon, fleuramon, dihydrojasmon, cis-jasmone, iso- E-Super®, methyl cedryl ketone or methyl citrate ion, acetophenone, methyl acetophenone,
  • the ketones may be selected from Alpha Damascon, Delta Damascone, Iso Damascone, Carvon, gamma-methyl ionone, Iso-E-Super, 2,4,4,7-tetramethyl-oct-6-en-3-one, Benzylacetone, Beta Damascone, Damascenone, methyl dihydrojasmonate, methyl cedrylon, hedione and mixtures thereof.
  • the component (b) in amounts of 0.001 wt .-% to 3 wt .-%, preferably 0.01 to 2 wt .-%, in particular 0.1 to 1 wt .-% in the mean, based on the total
  • an agent according to the invention contains 0.001% by weight to 3% by weight, preferably 0.01% to 2% by weight, in particular 0.1% to 1% by weight, of fragrance aldehydes,% by weight, based on the total agent, so is also a preferred embodiment of the invention.
  • the ratio of component (a) to component (b) is 25: 1 to 1: 5. Then again there is a preferred embodiment of the invention.
  • the total amount of fragrance of the agent, including all fragrance aldehydes contained 0.01 to 10 wt .-%, preferably 0.1 to 5 wt .-%, in particular 0.3 to 3 wt .-% is. This corresponds to a preferred embodiment of the invention.
  • the agent according to the invention is in solid form, preferably in powder form or else in granular form or in the form of molded articles, for example tablets. But it is also possible that the inventive agent in in liquid form, preferably in gel form. This, too, corresponds to a preferred embodiment of the invention.
  • the composition according to the invention may comprise further suitable ingredients, but in particular surfactants.
  • surfactants may be described in more detail below.
  • Another object of the invention is a textile cleaning or conditioning process in which the textile to be cleaned is subjected to textile washing using a washing, cleaning or care agent according to the invention, in particular in an automatic washing machine, preferably at temperatures above 6O 0 C, in particular not 4O 0 C.
  • Another object of the invention is the use of a washing, cleaning or care agent according to the invention for cleaning and / or conditioning of textile fabrics, in particular in an automatic washing machine, preferably at temperatures not above 6O 0 C, in particular not above 40 0 C. ,
  • Another object of the invention is the use of (optionally substituted) ethylenediamine and / or (optionally substituted) propylenediamine as a separately added component in perfume-containing detergents, cleaning or care products containing fragrance aldehyde, to extend the fragrance effect of the wash , Cleaning or care products.
  • fragrance aldehydes likewise contained and is intended to mean that ethylenediamine and / or (optionally substituted) propylenediamine and fragrance aldehydes enter the washing, cleaning or care agent as separate entities to introduce the components (a) and (b) into the product in a single step, eg together with the rest of the perfuming, provided that the components (a) and (b) are present separately during the addition, for example as separate components of a perfume oil.
  • Another object of the invention is the use of (optionally substituted) ethylenediamine and / or (optionally substituted) propylenediamine as a separately added component in perfume-containing detergents, cleaning or care products containing fragrance aldehyde, to achieve a long-lasting fresh smell at the application of the washing, Cleaning or care products.
  • "Separately added component" is to be understood as previously described.
  • the washing, cleaning or care agent may in particular be a textile treatment agent in the form of a textile detergent, fabric conditioner, softening detergent or washing aid. It may also be e.g. to be a hard surface cleaning agent, such as preferably a dishwashing detergent, especially a machine dishwashing detergent. It may also be detergents, e.g. Household cleaners, all-purpose cleaners, window cleaners, floor cleaners, etc. act. Preferably, it may be a
  • the care agent is preferably cosmetics, e.g. Hair shampoos, deodorants, etc., which can be used for personal care and / or cleaning.
  • the care product may also be air care products and room air improvers.
  • the agent according to the invention is therefore a textile treatment agent, an ironing aid, a cleaning cloth, a laundry detergent, a softener, a cleaning agent, in particular for hard and / or soft surfaces, a household cleaner, a care agent, a laundry care product Room fragrancing agent, an air freshener, a conditioning agent, a coloring agent, a fabric softener, a conditioning substrate, a cleaning agent, a cosmetic, a bleach, a descaling agent, a car care product, floor care products, stoves, leather care products, furniture care products, a scouring agent, a disinfectant Scenting agent, a mold remover and / or a precursor of the aforementioned means. It is an advantage of the invention that the agents according to the invention are very stable on storage.
  • the composition according to the invention contains additional fragrance (s), in particular selected from the group consisting of fragrances of natural or synthetic origin, preferably more volatile fragrances, higher-boiling fragrances, solid fragrances and / or strong fragrances.
  • additional fragrance in particular selected from the group consisting of fragrances of natural or synthetic origin, preferably more volatile fragrances, higher-boiling fragrances, solid fragrances and / or strong fragrances.
  • Adherent fragrances which are advantageously used in the present invention are, for example, essential oils such as angelica root oil, aniseed oil, arnica blossom oil, basil oil, bay oil, bergamot oil, Champacablütenöl, Edeltannöl, Edeltannenzapfen oil, Elemiöl, eucalyptus oil, fennel oil, spruce oil, galbanum oil, geranium oil, gingergrass oil , Guaiac wood oil, gurdy balm oil, helichrysum oil, ho oil, ginger oil, iris oil, cajeput oil, calamus oil, chamomile oil, Camphor oil, kanga oil, cardamom oil, cassia oil, pine oil, copaiba balsam, coriander oil, spearmint oil, caraway oil, cumin oil, lavender oil, lemon grass oil, lime oil, tangerine oil, lemon balm oil, musk kernel oil, myrrh oil, clove oil, neroli oil,
  • fragrances can be used in the context of the present invention as adherent fragrances or fragrance mixtures, ie fragrances.
  • These compounds include the following compounds and mixtures thereof: ambrettolide, ⁇ -amylcinnamaldehyde, anethole, anisaldehyde, anisalcohol, anisole, methyl anthranilate, acetophenone, benzylacetone, benzaldehyde, ethyl benzoate, benzophenone, benzyl alcohol, benzyl acetate, benzyl benzoate, benzyl formate, benzyl valerate, borneol , Bornyl acetate, ⁇ -bromostyrene, n-decyl aldehyde, n-dodecyl aldehyde, Eugenof, eugenol methyl ether, eucalyptol, farnesol,
  • the more volatile fragrances include, in particular, the lower-boiling fragrances of natural or synthetic origin, which can be used alone or in mixtures.
  • Examples of more volatile fragrances are alkyl isothiocyanates (alkylmustard oils), butanedione, limonene, linalool, linayl acetate and propionate, menthol, menthone, methyl-n-heptenone, phellandrene, phenylacetaldehyde, terpinyl acetate, citral, citronellal.
  • the agent according to the invention comprises supported and / or encapsulated perfume.
  • the washing, care or cleaning agent according to the invention comprises at least one, preferably several, active components, in particular washing, care, cleaning and / or cosmetic components, advantageously selected from the group comprising anionic surfactants, cationic surfactants, amphoteric surfactants, nonionic surfactants, acidifying agents, alkalizing agents, anti-wrinkling compounds, antibacterial agents, antioxidants, anti redeposition agents, antistatic agents, builders, bleaches, bleach activators, bleach stabilizers, bleach catalysts, ironing aids, cobuilders, fragrances, anti-shrinkage agents, electrolyte, enzymes, colorants, Colorants, dyes, color transfer inhibitors, fluorescers, fungicides, germicides, odor-complexing agents, adjuvants, hydrotropes, rinse aids, chelating agents, preservatives, corrosion inhibitors, water-miscible organic Solvents, optical brighteners, perfumes, perfume carriers, pearlescers, pH adjusters,
  • the surfactant content will be higher or lower.
  • the surfactant content of, for example, detergents is between 10 and 50% by weight, preferably between 12.5 and 30% by weight, and more preferably between 15 and 25% by weight, while automatic dishwashing detergents e.g. between 0.1 and 10 wt .-%, preferably between 0.5 and 7.5 wt .-% and in particular between 1 and 5 wt .-% surfactants may contain.
  • compositions of the invention may contain surfactants, with preference being given to anionic surfactants, nonionic surfactants and mixtures thereof, as well as cationic surfactants.
  • Suitable nonionic surfactants are, in particular, ethoxylation and / or propoxylation products of alkyl glycosides and / or linear or branched alcohols having in each case 12 to 18 C atoms in the alkyl moiety and 3 to 20, preferably 4 to 10, alkyl ether groups.
  • Suitable ethoxylation and / or propoxylation products of N-alkylamines, vicinal diols, fatty acid esters and fatty acid amides which correspond to said long-chain alcohol derivatives with respect to the alkyl moiety and of alkylphenols having 5 to 12 carbon atoms in the alkyl radical are useful.
  • Suitable anionic surfactants are in particular soaps and those which contain sulfate or sulfonate groups with preferably alkali ions as cations.
  • Usable soaps are preferably the alkali salts of the saturated or unsaturated fatty acids having 12 to 18 carbon atoms. Such fatty acids can also be used in incompletely neutralized form.
  • Useful surfactants of the sulfate type include the salts of the sulfuric acid half-esters of fatty alcohols having 12 to 18 carbon atoms and the sulfation products of said nonionic surfactants having a low degree of ethoxylation.
  • Suitable surfactants of the sulfonate type include linear alkylbenzenesulfonates having 9 to 14 carbon atoms in the alkyl moiety, alkanesulfonates having 12 to 18 carbon atoms, and olefin sulfonates having 12 to 18 carbon atoms, which are formed in the reaction of corresponding monoolefins with sulfur trioxide, and alpha-sulfofatty acid esters resulting from the sulfonation of fatty acid methyl or ethyl esters.
  • Cationic surfactants are preferably selected from esterquats and / or quaternary ammonium compounds (QAV) according to the general formula (R ') (R ") (R"') (R IV ) N + X - , in which R 1 to R iv for the same or different C
  • QAV quaternary ammonium compounds
  • the heterocycle such as a pyridinium or Imidazoliniumeducating, form, and X " for halide ions, sulfate ions, hydroxide ions or similar anions
  • QACs can be prepared by reaction of tertiary amines with alkylating agents, such as, for example, methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also ethylene oxide.
  • alkylating agents such as, for example, methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also ethylene oxide.
  • Eligible QACs include benzalkone ium chloride (N alkyl-N, N dimethylbenzylammonium chloride), benzalkone B (m, p-dichlorobenzyldimethyl-C 12 -alkylammonium chloride, benzoxonium chloride (benzyldodecyl-bis- (2-hydroxyethyl) -ammonium chloride), cetrimonium bromide (N- Hexadecyl-N, N-trimethyl-ammonium bromide), benzetonium chloride (N, N-dimethyl-N [2- [2- [2- [p- (1,1,3,3-tetramethyl-butyl) -phenoxy] -ethoxy] -ethyl] -benzylammonium chloride)
  • Esterquats are here preferably compounds of the general formula IV, RS (CO) -C (CH 2 ) s X " (
  • R 5 is an alkyl or alkenyl radical having 12 to 22 carbon atoms and 0, 1, 2 or 3 double bonds
  • R 6 and R 7 are independently H, OH or O (CO)
  • R 5 , s, t and u are each independently of the other the value 1, 2 or 3
  • X is an anion, in particular halide, methosulphate, methophosphate or phosphate and mixtures thereof
  • R 6 are the group O (CO) R 5 and for R 5 contain an alkyl radical having 16 to 18 carbon atoms
  • R 7 additionally represents OH.
  • Examples of compounds of the formula (IV) are methyl N- (2-hydroxyethyl) -N, N di (tallow acyl oxyethyl) ammonium methosulfate, bis (palmitoyl) ethyl hydroxyethyl methyl ammonium methosulfate or methyl N, N-bis (acyloxyethyl) -N- (2-hydroxyethyl) ammonium methosulfate If quaternized compounds of the formula (IV) which have unsaturated groups are used, the acyl groups whose k corresponding fatty acids have an iodine value between 5 and 80, preferably between 10 and 60 and in particular between 15 and 45 and / or which has a cis / trans isomer ratio (in mol%) of greater than 30:70, preferably greater than 50:50 and in particular greater than 70:30.
  • alkylammoniummethosulfate marketed by Stepan under the trade name Stepantex® ® methyl hydroxyalkyl or known under the trade name Dehyquart® ® products from Cognis Germany GmbH or the known under the name Rewoquat ® products by manufacturer Goldschmidt-Witco.
  • Surfactants are present in the inventive compositions in proportions of preferably 5 wt .-% to 50 wt .-%, in particular from 8 wt .-% to 30 wt .-%. Particularly in laundering agents, preferably up to 30% by weight, in particular from 5% by weight to 15% by weight, of surfactants, among these preferably at least partially cationic surfactants, are used.
  • An agent according to the invention preferably contains at least one water-soluble and / or water-insoluble, organic and / or inorganic builder.
  • the water-soluble organic builder substances include polycarboxylic acids, in particular citric acid and sugar acids, monomeric and polymeric aminopolycarboxylic acids, in particular methylglycine diacetic acid, nitrilotriacetic acid and ethylenediaminetetraacetic acid and polyaspartic acid, polyphosphonic acids, in particular aminotris (methylenephosphonic acid), ethylenediaminetetrakis (methylenephosphonic acid) and 1-hydroxyethane-1, 1-diphosphonic acid, polymeric hydroxy compounds such as dextrin and also polymeric (poly) carboxylic acids, polymeric acrylic acids, methacrylic acids, maleic acids and mixed polymers thereof, which also polymerize small amounts May contain copolymerized substances without carboxylic acid functionality.
  • the molecular weight of the homopolymers of unsaturated carboxylic acids is generally between 5,000 and 200,000, that of the copolymers between 2,000 and 200,000, preferably 50,000 to 120,000, in each case based on the free acid.
  • a particularly preferred acrylic acid-maleic acid copolymer has a molecular weight of 50,000 to 100,000.
  • Suitable, albeit less preferred, compounds of this class are copolymers of acrylic acid or methacrylic acid with vinyl ethers, such as vinylmethyl ethers, vinyl esters, ethylene, propylene and styrene, in which the proportion of the acid is at least 50% by weight.
  • the first acidic monomer or its salt is derived from a monoethylenically unsaturated C 3 -C 8 -carboxylic acid and preferably from a C 3 - C 4 -monocarboxylic acid, in particular from (meth) -acrylic acid.
  • the second acidic monomer or its salt can be a derivative of a C 4 -C 8 -dicarboxylic acid, with maleic acid being particularly preferred.
  • the third monomeric unit is formed in this case of vinyl alcohol and / or preferably an esterified vinyl alcohol.
  • vinyl alcohol derivatives are preferred which represent an ester of short-chain carboxylic acids, for example of C 1 -C 4 -carboxylic acids, with vinyl alcohol.
  • Preferred polymers contain from 60% by weight to 95% by weight, in particular from 70% by weight to 90% by weight, of (meth) acrylic acid or (meth) acrylate, particularly preferably acrylic acid or acrylate, and maleic acid or Maleinate and 5 wt .-% to 40% by weight, preferably 10 wt .-% to 30 wt .-% of vinyl alcohol and / or vinyl acetate.
  • the second acidic monomer or its salt can also be a derivative of an allylsulfonic acid which is substituted in the 2-position by an alkyl radical, preferably by a C 1 -C 4 -alkyl radical, or by an aromatic radical which is preferably derived from benzene or benzene derivatives
  • Preferred terpolymers contain from 40% by weight to 60% by weight, in particular from 45 to 55% by weight, of (meth) acrylic acid or (meth) acrylate, particularly preferably acrylic acid or acrylate, from 10% by weight to 30% by weight.
  • % preferably 15 wt .-% to 25 wt .-% methallylsulfonic acid or Methallylsulfonat and as the third monomer 15 wt .-% to 40 wt .-%, preferably 20 wt .-% to 40 wt .-% of a carbohydrate.
  • This carbohydrate may be, for example, a mono-, di-, oligo- or polysaccharide, mono-, di- or oligosaccharides being preferred. Particularly preferred is sucrose.
  • the use of the third monomer presumably incorporates predetermined breaking points into the polymer which are responsible for the good biodegradability of the polymer.
  • terpolymers generally have a molecular weight between 1,000 and 200,000, preferably between 200 and 50,000 and especially between 3 000 and 10 000 on.
  • Further preferred copolymers are those which contain acrolein and acrylic acid / acrylic acid salts or vinyl acetate as monomers.
  • the organic builder substances can be used, in particular for the preparation of liquid agents, in the form of aqueous solutions, preferably in the form of 30 to 50 percent by weight aqueous solutions. All of the acids mentioned are generally used in the form of their water-soluble salts, in particular their alkali metal salts.
  • organic builder substances may be present in amounts of up to 40% by weight, in particular up to 25% by weight and preferably from 1% by weight to 8% by weight. Quantities close to the stated upper limit are preferably used in paste-form or liquid, in particular water-containing, agents according to the invention. Aftertreatment agents according to the invention, such as e.g. Softener, may optionally also be free of organic builder.
  • Suitable water-soluble inorganic builder materials are, in particular, alkali metal silicates and polyphosphates, preferably sodium triphosphate. Crystalline or amorphous alkali metal nanosilicates, if desired in amounts of up to 50% by weight, preferably not more than 40% by weight and in liquid media, in particular from 1% by weight to 5% by weight, can be used as water-insoluble, water-dispersible inorganic builder materials. -%, are used. Among these, preferred are the detergent grade crystalline sodium aluminosilicates, especially zeolite A, P and optionally X. Amounts near the above upper limit are preferably used in solid, particulate agents. In particular, suitable aluminosilicates have no particles with a particle size greater than 30 .mu.m and preferably consist of at least 80% by weight of particles having a size of less than 10 .mu.m.
  • Suitable substitutes or partial substitutes for the said aluminosilicate are crystalline alkali silicates which may be present alone or in a mixture with amorphous silicates.
  • the alkali metal silicates useful as builders in the compositions according to the invention preferably have a molar ratio of alkali metal oxide to SiO 2 of less than 0.95, in particular of 1: 1, 1 to 1: 12, and may be amorphous or crystalline.
  • Preferred alkali metal silicates are the sodium silicates, in particular the amorphous sodium silicates, with a molar ratio of Na 2 O: SiO 2 of 1: 2 to 1: 2.8.
  • the crystalline silicates which may be present alone or in admixture with amorphous silicates, are crystalline layer silicates with the general formula Na 2 Si x O y are used 2x + 1 H 2 O, in which x, known as the modulus, an integer of 1, 9 to 4 and y is a number from 0 to 20 and preferred values for x are 2, 3 or 4.
  • Preferred crystalline phyllosilicates are those in which x in the abovementioned general formula assumes the values 2 or 3. In particular, both ⁇ - and ⁇ -sodium disilicates (Na 2 Si 2 O 5 y H 2 O) are preferred.
  • amorphous alkali silicates practically anhydrous crystalline alkali silicates of the above general Formula in which x is a number from 1, 9 to 2.1, can be used in inventive compositions.
  • a crystalline sodium layer silicate with a modulus of 2 to 3 is used, as can be prepared from sand and soda.
  • Crystalline sodium silicates with a modulus in the range of 1.9 to 3.5 are used in a further preferred embodiment of compositions according to the invention.
  • the weight ratio of aluminosilicate to silicate is preferably 1:10 to 10: 1.
  • the weight ratio of amorphous alkali metal silicate to crystalline alkali metal silicate is preferably 1: 2 to 2: 1 and especially 1: 1 to 2: 1.
  • builder substances are preferably present in the compositions according to the invention in amounts of up to 60% by weight, in particular from 5% by weight to 40% by weight.
  • Aftertreatment agents according to the invention such as e.g. Softener, are preferably free of inorganic builder.
  • Suitable peroxygen compounds are, in particular, organic peracids or pers acid salts of organic acids, such as phthalimidopercaproic acid, perbenzoic acid or salts of diperdodecanedioic acid, hydrogen peroxide and inorganic salts which release hydrogen peroxide under the conditions of use, such as perborate, percarbonate and / or persilicate.
  • organic peracids or pers acid salts of organic acids such as phthalimidopercaproic acid, perbenzoic acid or salts of diperdodecanedioic acid, hydrogen peroxide and inorganic salts which release hydrogen peroxide under the conditions of use, such as perborate, percarbonate and / or persilicate.
  • solid peroxygen compounds can be used in the form of powders or granules, which can also be enveloped in a manner known in principle.
  • alkali percarbonate alkali perborate monohydrate or, in particular, in liquid media
  • hydrogen peroxide in the form of aqueous solutions containing from 3% by weight to 10% by weight of hydrogen peroxide.
  • an agent according to the invention contains bleaches, such as preferably peroxygen compounds, they are present in amounts of preferably up to 50% by weight, in particular from 5% by weight to 30% by weight.
  • bleach stabilizers such as phosphonates, borates or metaborates and metasilicates and magnesium salts such as magnesium sulfate may be useful.
  • bleach activators it is possible to use compounds which, under perhydrolysis conditions, give aliphatic peroxycarboxylic acids having preferably 1 to 10 C atoms, in particular 2 to 4 C atoms, and / or optionally substituted perbenzoic acid.
  • Suitable substances are those which carry O- and / or N-acyl groups of the stated C atom number and / or optionally substituted benzoyl groups.
  • polyacylated alkylenediamines in particular tetraacetylethylenediamine (TAED), acylated triazine derivatives, in particular 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine (DADHT), acylated glycolurils, in particular tetraacetylenediamines.
  • TAED tetraacetylethylenediamine
  • DADHT 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine
  • acylated glycolurils in particular tetraacetylenediamines.
  • acetylglycoluril TAA
  • N-acylimides N-nonanoylsuccinimide (NOSI)
  • NOSI N-nonanoylsuccinimide
  • acylated phenolsulfonates in particular n-nonanoyl or isononanoyloxybenzenesulfonate (n- or iso-NOBS)
  • carboxylic anhydrides in particular phthalic anhydride
  • acylated polyhydric alcohols in particular triacetin, ethylene glycol diacetate , 2,5-diacetoxy-2,5-dihydrofuran and enol esters, as well as acetylated sorbitol and mannitol or mixtures thereof (SORMAN)
  • acylated sugar derivatives in particular pentaacetylglucose (PAG), pentaacetyl fructose, tetraacetylxylose and
  • Hydrophilic substituted acyl acetals and acyl lactams are also preferably used.
  • Combinations of conventional bleach activators can also be used. Such bleach activators may be present in the customary amount range, preferably in amounts of from 1% by weight to 10% by weight, in particular from 2% by weight to 8% by weight, based on the total agent.
  • sulfone imines and / or bleach-enhancing transition metal salts or transition metal complexes can also be present as so-called bleach catalysts.
  • Suitable transition metal compounds include, in particular, manganese, iron, cobalt, ruthenium or molybdenum-salene complexes and their N-analogues, manganese, iron, cobalt, ruthenium or molybdenum carbonyl complexes, manganese, iron, , Cobalt, ruthenium, molybdenum, titanium, vanadium, and copper complexes with nitrogen-containing tripod ligands, cobalt, iron, copper, and ruthenium-ammine complexes.
  • Bleach-enhancing transition metal complexes in particular having the central atoms Mn, Fe, Co, Cu, Mo, V, Ti and / or Ru, can be used in customary amounts, preferably in an amount of up to 1% by weight, in particular 0.0025% by weight. % to 0.25 wt .-% and particularly preferably from 0.01 wt .-% to 0.1 wt .-%, each based on the total agent used.
  • Suitable enzymes which can be used in the compositions are those from the class of proteases, cutinases, amylases, pullulanases, hemicellulases, cellulases, lipases, oxidases and peroxidases and mixtures thereof. Particularly suitable are from fungi or bacteria, such as Bacillus subtilis, Bacillus licheniformis, Streptomyces griseus, Humicola lanuginosa, Humicola insolens, Pseudomonas pseudoalcaligenes or Pseudomonas cepacia derived enzymatic agents.
  • the optionally used enzymes may be adsorbed to carriers and / or embedded in encapsulants to protect against premature inactivation.
  • the agents may contain, for example, derivatives of diaminostilbenedisulfonic acid or their alkali metal salts as optical brighteners.
  • salts of 4,4'-bis (2-anilino-4-morpholino-1, 3,5-triazinyl-6-annino) stilbene-2,2'-disulphonic acid or similarly constructed compounds which replace the morpholino Group carry a diethanolamino group, a methylamino group, an anilino group or a 2-methoxyethylamino group.
  • brighteners of the substituted diphenylstyrene type may be present, for example the alkali metal salts of 4,4'-bis (2-sulfostyryl) -diphenyl, 4,4'-bis (4-chloro-3-sulfostyryl) -diphenyl or 4- (4-chlorostyryl) -4 '- (2-sulfostyryl) -diphenyls. Mixtures of the aforementioned brightener can be used.
  • Suitable foam inhibitors include, for example, organopolysiloxanes and mixtures thereof with microfine, optionally signed silica and also Pa raffinwachse and mixtures thereof with silanated silica or bis-fatty acid alkylenediamides. It is also advantageous to use mixtures of various foam inhibitors, for example those of silicones, paraffins or waxes.
  • the foam inhibitors in particular silicone and / or paraffin-containing foam inhibitors, are bound to a granular, water-soluble or dispersible carrier substance.
  • mixtures of paraffin waxes and bistearylethylenediamides are preferred.
  • compositions may also contain components which positively influence the oil and Fettauswaschles from textiles, so-called soil release agents. This effect becomes particularly evident when a textile is soiled which has previously been washed several times with an agent according to the invention containing this oil and fat-dissolving component.
  • the preferred oil and fat dissolving components include, for example, nonionic cellulose ethers such as methylcellulose and methylhydroxypropylcellulose with a proportion of methoxyl groups of 15 to 30 wt .-% and hydroxypropoxyl groups of 1 to 15 wt .-%, each based on the nonionic Cellulose ethers, and the known from the prior art polymers of phthalic acid and / or terephthalic acid or derivatives thereof with monomeric and / or polymeric diols, in particular polymers of ethylene terephthalates and / or polyethylene glycol terephthalates or anionic and / or nonionic modified derivatives thereof.
  • nonionic cellulose ethers such as methylcellulose and methylhydroxypropylcellulose with a proportion of methoxyl groups of 15 to 30 wt .-% and hydroxypropoxyl groups of 1 to 15 wt .-%, each based on the nonionic Cellulose ethers
  • compositions may also color transfer inhibitors, preferably in amounts of from 0.1 wt .-% to 2 wt .-%, in particular 0.1 wt .-% to 1 wt .-%, containing in a preferred embodiment of the invention polymers Vinylpyrrolidone, vinylimidazole, vinylpyridine N-oxide or copolymers of these are.
  • polyvinylpyrrolidones having molecular weights of from 15,000 to 50,000 and polyvinylpyrrolidones having molecular weights of more than 1,000,000, in particular from 1,500,000 to 4,000,000, N-vinylimidazole / N-vinylpyrrolidone copolymers, polyvinyloxazolidones, Copolymers based on vinyl monomers and carboxamides, pyrrolidone group-containing polyesters and polyamides, grafted polyamidoamines and polyethyleneimines, polymers with amide groups of secondary amines, polyamine-N-oxide polymers, polyvinyl alcohols and copolymers based on acrylamidoalkenylsulfonic acids.
  • enzymatic systems comprising a peroxidase and hydrogen peroxide or a substance which gives off hydrogen peroxide in water.
  • a mediator compound for the peroxidase for example an acetosyringone, a phenol derivative or a phenotiazine or phenoxazine, is preferred in this case, whereby also above-mentioned polymeric Farbübertragungsinhibitorwirkstoffe can be used.
  • Polyvinylpyrrolidone preferably has an average molecular weight in the range from 10 000 to 60 000, in particular in the range from 25 000 to 50 000, for use in compositions according to the invention.
  • the copolymers those of vinylpyrrolidone and vinylimidazole in a molar ratio of 5: 1 to 1: 1 having an average molecular weight in the range of 5,000 to 50,000, especially 10,000 to 20,000 are preferred.
  • Graying inhibitors have the task of keeping suspended from the textile fiber dirt suspended in the fleet.
  • Water-soluble colloids of mostly organic nature are suitable for this purpose, for example starch, glue, gelatin, salts of ether carboxylic acids or ether sulfonic acids of starch or of cellulose or salts of acidic sulfuric acid esters of cellulose or starch.
  • water-soluble polyamides containing acidic groups are suitable for this purpose.
  • starch derivatives can be used, for example aldehyde starches.
  • cellulose ethers such as carboxymethylcellulose (Na salt), methylcellulose, hydroxyalkylcellulose and mixed ethers, such as methylhydroxyethylcellulose, methylhydroxypropylcellulose, methylcarboxymethylcellulose and mixtures thereof, for example in amounts of from 0.1 to 5% by weight, based on the compositions become.
  • organic solvents which can be used in the compositions according to the invention, especially if they are in liquid or pasty form, are alcohols having 1 to 4 C atoms, in particular methanol, ethanol, isopropanol and tert-butanol, diols having 2 to 4 C atoms , in particular ethylene glycol and propylene glycol, and mixtures thereof and the derivable from said classes of compound ethers.
  • Such water-miscible solvents are preferably present in the compositions according to the invention in amounts of not more than 30% by weight, in particular from 6% by weight to 20% by weight.
  • the compositions according to the invention may contain system and environmentally acceptable acids, in particular citric acid, acetic acid, tartaric acid, malic acid, lactic acid, glycolic acid, succinic acid, glutaric acid and / or adipic acid, but also mineral acids, especially particular sulfuric acid, or bases, in particular ammonium or alkali hydroxides.
  • Such pH regulators are preferably not more than 20 wt .-%, in particular from 1, 2 wt .-% to 17 wt .-%, contained in the inventive compositions.
  • compositions according to the invention presents no difficulties and can be carried out in a manner known in the art, for example by spray-drying or granulation, with optional peroxygen compound and optional bleach catalyst optionally being added later.
  • a process comprising an extrusion step is preferred.
  • the preparation of liquid inventive means also presents no difficulties and can also be done in a known manner.
  • the teaching according to the invention can be used to significantly reduce the perfume fraction in washing, cleaning and personal care products. This makes it possible to offer perfumed products even for those particularly sensitive consumers who can not use normally perfumed products due to special intolerances and irritations, or only to a limited extent. In this context, especially skin care products and deodorants, but also detergents, such. To call hand detergent.
  • a preferred solid, in particular powdered, detergent according to the invention can contain, in addition to the constituents according to the invention (ie, (a) fragrant aldehydes and (b) (optionally substituted) ethylenediamines and / or (optionally substituted) propylenediamines), in particular also components which are e.g. are selected from the following:
  • Anionic surfactants preferably alkylbenzenesulfonate, alkylsulfate, e.g. in amounts of preferably 5-30% by weight
  • Nonionic surfactants such as preferably fatty alcohol polyglycol ethers, alkylpolyglucoside, fatty acid glucamide, e.g. in amounts of preferably 0.5-15% by weight
  • Builders e.g. Zeolite, polycarboxylate, sodium citrate, in amounts of e.g. 0-70% by weight, advantageously 5-60% by weight, preferably 10-55% by weight, in particular 15-40% by weight,
  • Alkalis e.g. Sodium carbonate
  • Alkalis e.g. Sodium carbonate
  • amounts of e.g. 0-35 wt .-% advantageously 1-30 wt .-%, preferably 2-25 wt .-%, in particular 5-20 wt .-%,
  • Bleaching agents e.g. Sodium perborate, sodium percarbonate, in amounts of e.g. 0-30% by weight, advantageously 5-25% by weight, preferably 10-20% by weight,
  • - corrosion inhibitors e.g. Sodium silicate
  • amounts of e.g. 0-10% by weight advantageously 1-6% by weight, preferably 2-5% by weight, in particular 3-4% by weight,
  • Stabilizers eg phosphonates, advantageously 0-1% by weight
  • Foam inhibitor for example soap, silicone oils, paraffins, advantageously 0-4% by weight, preferably 0.1-3% by weight, in particular 0.2-1% by weight,
  • Enzymes e.g. Proteases, amylases, cellulases, lipases, advantageously 0-2% by weight, preferably 0.2-1% by weight, in particular 0.3-0.8% by weight,
  • - grayness inhibitor e.g. Carboxymethylcellulose, advantageously 0-1% by weight
  • Discoloration inhibitor e.g. Polyvinylpyrrolidone derivatives, preferably 0-2% by weight,
  • Optical brighteners e.g. Stilbene derivative, biphenyl derivative, advantageously 0-0.4% by weight, in particular 0.1-0.3% by weight,
  • the washing, cleaning or care agent is in liquid form, preferably in gel form.
  • Preferred liquid washing, cleaning or care agents have water contents of e.g. 10-95 wt .-%, preferably 20-80 wt .-% and in particular 30-70 wt .-%, based on the total agent.
  • the water content may also be particularly low, e.g. ⁇ 30 wt .-%, preferably ⁇ 20 wt .-%, in particular ⁇ 15 wt .-%, wt .-% in each case based on the total agent.
  • the liquid agents may also contain non-aqueous solvents.
  • a preferred liquid, in particular gel detergent according to the invention may contain, in particular, components which are e.g. are selected from the following:
  • Anionic surfactants preferably alkylbenzenesulfonate, alkylsulfate, e.g. in amounts of preferably 5-40% by weight
  • Nonionic surfactants such as preferably fatty alcohol polyglycol ethers, alkylpolyglucoside, fatty acid glucamide, e.g. in amounts of preferably 0.5-25% by weight
  • Builders e.g. Zeolite, polycarboxylate, sodium citrate, advantageously 0-15% by weight, preferably 0.01-10% by weight, in particular 0.1-5% by weight,
  • Foam inhibitor e.g. Soap, silicone oils, paraffins, in amounts of e.g. 0-10 wt .-%, advantageously 0.1-4 wt .-%, preferably 0.2-2 wt .-%, in particular 1-3 wt .-%,
  • Enzymes for example proteases, amylases, cellulases, lipases, in amounts of, for example, 0-3 wt .-%, advantageously 0.1-2 wt .-%, preferably 0.2-1 wt .-%, in particular 0.3 -0.8% by weight
  • Optical brightener eg stilbene derivative, biphenyl derivative, in amounts of eg 0-1% by weight, advantageously 0.1-0.3% by weight, in particular 0.1-0.4% by weight .
  • optionally soap in quantities of e.g. 0-25% by weight, advantageously 1-20% by weight, preferably 2-15% by weight, in particular 5-10% by weight,
  • solvents preferably alcohols
  • solvents advantageously 0-25 wt .-%, preferably 1-20 wt .-%, in particular 2-15 wt .-%, wt .-% in each case based on the total agent.
  • a preferred liquid softener according to the invention may in particular also contain components which are selected from the following:
  • Cationic surfactants such as in particular esterquats, e.g. in amounts of 5-30% by weight,
  • Cosurfactants e.g. Glycerol monostearate, stearic acid, fatty alcohols, fatty alcohol ethoxylates, e.g. in amounts of 0-5% by weight, preferably 0.1-4% by weight,
  • Emulsifiers e.g. Fatty amine ethoxylates, e.g. in amounts of 0-4 wt .-%, preferably
  • Stabilizers preferably in the ppm range
  • Solvents in particular water, in amounts of preferably 60-90% by weight,
  • the washed laundry was then submitted to a panel of 7 people trained by the smell, who assessed the intensity of the laundry smell in the wet state as well as in the dry state (7 days after the laundry).
  • the wet laundry was previously dried on a leash and, after drying, folded and stored in an open rack until 7 days had elapsed since the laundry.
  • the laundry detergent B which was in accordance with the invention consequently resulted in a significantly improved fragrance intensity in the dry laundry after 7 days, compared with laundry detergent A.
  • the fragrance effect of a commercial liquid softener was investigated, which contained 0.9 wt .-% octanal. This corresponds to the softener A. Also, the fragrance effect of an otherwise comparable commercial liquid softener was examined, which also contained 0.9 wt .-% octanal. This fabric softener also containing 1, 4 wt .-% N, N '- Dimethylethylendiannin. This corresponds to the fabric softener B.
  • the washed laundry was then in turn submitted to a panel of 7 people with an olfactory education, who assessed the intensity of the laundry odor in the wet state and in the dry state (7 days after washing), analogous to the investigation of the detergent, as already described.
  • the softener B consistent with the invention consequently resulted in a significantly improved fragrance intensity in the dry laundry after 7 days compared to fabric softener A.

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Abstract

The invention relates to an odor-imparting detergent, cleaning or care product which contains odoriferous aldehydes and (optionally substituted) ethylene diamine and/or (optionally substituted) propylene diamine, allowing surprising odor advantages of the objects treated therewith, especially in terms of intensity and lasting nature of the odor impression. The total amount of perfume which the product should contain can even be reduced and yet odor advantages can be achieved on the objects.

Description

Duftgebendes Wasch-, Reinigungs- oder Pflegemittel Scented washing, cleaning or care products

Die vorliegende Erfindung betrifft ein Wasch-, Reinigungs- oder Pflegemittel, enthaltend Ethylendiamine und/oder Propylendiamine. Sie betrifft ferner ein Textilreinigungs- oder konditionierverfahren, bei welchem das zu reinigende Textil einer Textilwäsche unter Einsatz eines entsprechenden Wasch-, Reinigungs- oder Pflegemittels unterworfen wird. Sie betrifft die Verwendung eines solchen Mittels zum Reinigen und/oder Konditionieren von textilen Flächengebilden, insbesondere in einer automatischen Waschmaschine. Sie betrifft die Verwendung von Ethylendiamin und/oder Propylendiamin zur Verlängerung der Duftwirkung des Wasch-, Reinigungs- oder Pflegemittels sowie zur Erzielung eines lange anhaltenden Frischegeruches bei der Anwendung des Wasch-, Reinigungs- oder Pflegemittels.The present invention relates to a washing, cleaning or care agent containing ethylenediamines and / or propylenediamines. It further relates to a textile cleaning or conditioning method in which the textile to be cleaned is subjected to a textile washing using an appropriate washing, cleaning or care agent. It relates to the use of such an agent for cleaning and / or conditioning of textile fabrics, in particular in an automatic washing machine. It relates to the use of ethylenediamine and / or propylenediamine to extend the fragrance effect of the washing, cleaning or care product as well as to achieve a long-lasting fresh scent when using the washing, cleaning or care product.

Bei der Anwendung von Wasch-, Reinigungs- oder Pflegemitteln verfolgt der Verbraucher nicht nur das Ziel, die zu behandelnden Objekte zu waschen, reinigen oder pflegen, sondern er wünscht sich auch, dass die behandelten Objekte, wie z.B. Textilien, nach der Wäsche gut riechen mögen. Insbesondere aus diesem Grunde enthalten die meisten kommerziell verfügbaren Wasch-, Reinigungs- oder Pflegemittel Riechstoffe.In the application of washing, cleaning or care products, the consumer not only pursues the goal of washing, cleaning or caring for the objects to be treated, but also desires that the treated objects, e.g. Textiles, like to smell good after washing. For this reason in particular, most commercially available washing, cleaning or care products contain fragrances.

Beim Einsatz herkömmlicher Wasch-, Reinigungs- oder Pflegemittel bleibt nach der Anwendung, insbesondere nach dem Waschen, jedoch oft nur ein verhältnismäßig schwacher Duft auf dem behandelten Objekt, wie insbesondere der Wäsche, zurück. Daher besteht auf Verbraucherseite ein fortwährendes Bedürfnis nach Wasch-, Reinigungs- oder Pflegemitteln, welche eine verbesserte Objektbeduftung, insbesondere Textilbeduftung, ermöglichen, vor allem mit Blick auf die Duftintensität, insbesondere hinsichtlich eines Frischeempfindens.When using conventional washing, cleaning or care products, however, often remains after use, especially after washing, but only a relatively weak scent on the treated object, in particular the laundry, back. Therefore, there is a continuing need for washing, cleaning or care products on the consumer side, which allow improved object scenting, in particular textile fragrancing, especially with regard to the scent intensity, in particular with regard to a sense of freshness.

Die Aufgabe der vorliegenden Erfindung war es daher, Wasch-, Reinigungs- oder Pflegemittel bereitzustellen, welche eine verbesserte Duftintensität bei der Anwendung, insbesondere im Zusammenhang mit der Textilbehandlung, zeigen.The object of the present invention was therefore to provide washing, cleaning or care products which show improved fragrance intensity during use, in particular in connection with textile treatment.

Diese Aufgabe wurde gelöst von einem Wasch-, Reinigungs- oder Pflegemittel, enthaltendThis object has been achieved by a washing, cleaning or care product containing

(a) Duftaldehyde sowie(a) fragrance aldehydes as well

(b) (ggf. substituierte) Ethylendiamine und/oder (ggf. substituierte) Propylendiamine. Es konnte überraschend gefunden werden, dass die erfindungsgemäßen Wasch-, Reinigungsoder Pflegemittel bei der Anwendung eine verbesserte Duftintensität zeigen, insbesondere im Zusammenhang mit der Textilbehandlung. Z.B. konnte bei der Anwendung eines erfindungsgemäßen Wäschebehandlungsmittels, wie z.B. Waschmittel sowie Weichspüler, eine verbesserte Duftintensität der behandelten Wäsche gefunden werden. Dies gilt sowohl für die feuchte wie insbesondere auch für die trockene Wäsche. Hierbei wurde auch eine bessere Dauerhaftigkeit des Dufteindruckes gefunden, d.h. der gewünschte Dufteindruck hielt länger vor. Ferner weisen entsprechende Produkte eine besonders gute Lagerstabilität auf. Die erfindungsgemäßen Mittel ermöglichen es zudem, die Gesamtmenge an Parfüm, welche im Mittel enthalten ist, zu reduzieren, und dennoch Geruchsvorteile auf den gewaschenen Textilien zu erzielen, insbesondere mit Blick auf das Frischeempfinden.(b) (optionally substituted) ethylenediamines and / or (optionally substituted) propylenediamines. It has surprisingly been found that the washing, cleaning or care agents according to the invention exhibit an improved fragrance intensity during use, in particular in connection with the textile treatment. For example, when using a laundry treatment agent according to the invention, such as detergents and fabric softeners, an improved fragrance intensity of the treated laundry could be found. This applies to both wet and especially dry laundry. Here also a better durability of the scent impression was found, ie the desired scent impression lasted longer. Furthermore, corresponding products have a particularly good storage stability. In addition, the compositions according to the invention make it possible to reduce the total amount of perfume which is contained on average, and nevertheless to achieve odor advantages on the laundered textiles, in particular with regard to the sensation of freshness.

In einer bevorzugten Ausführungsform der Erfindung zeichnet sich ein erfindungsgemäßes Mittel dadurch aus, dass die Komponente (a) und die Komponente (b) getrennt in die Wasch-, Reinigungs- oder Pflegemittelmatrix zugegeben werden. Bei dieser Vorgehensweise werden besonders vorteilhafte Duftintensitäten im erfindungsgemäßen Sinne ermöglicht. Es ist z.B. erfindungsgemäß möglich, die Komponente (a) mit der übrigen Parfümierung in das Produkt einzubringen und die Komponente (b) in einem gesonderten Schritt einzubringen. Weiterhin ist es auch erfindungsgemäß möglich, die Komponenten (a) und (b) in einem einzigen Schritt in das Produkt einzubringen, z.B. zusammen mit der übrigen Parfümierung, sofern die Komponenten (a) und (b) bei der Zugabe getrennt vorliegen, z.B. als separate Komponenten eines Parfümöls.In a preferred embodiment of the invention, an agent according to the invention is characterized in that component (a) and component (b) are added separately to the washing, cleaning or care agent matrix. In this procedure, particularly advantageous scent intensities in the sense of the invention are made possible. It is e.g. According to the invention possible to introduce the component (a) with the rest of perfuming in the product and to introduce the component (b) in a separate step. Furthermore, it is also possible according to the invention to introduce components (a) and (b) into the product in a single step, e.g. together with the remainder of the perfume, provided that components (a) and (b) are separate when added, e.g. as separate components of a perfume oil.

Gemäß einer weiteren bevorzugten Ausführungsform wird als Komponente (b) 1 ,2-Diaminoethan, Propan-1 ,3-diamin, 1 ,2-Dianilinoethan, N,N'-Dimethylethylendiamin, N, N'-Diethylethyl-1 ,3-diamin, N, N'-Diisopropylethyl-1 ,3-diamin, N,N'-Dimethylpropan-1 ,3-diamin, N, N'-Diethylpropan-1 ,3-diamin und/oder N, N'-Diisopropylpropan-1 ,3-diamin eingesetzt.In accordance with another preferred embodiment, the component (b) 1, 2-diaminoethane, propane-1, 3-diamine, 1, 2-dianilinoethane, N, N '-dimethylethylenediamine, N, N'-diethyl ethyl-1, 3-diamine , N, N'-Diisopropylethyl-1, 3-diamine, N, N '-Dimethylpropan-1, 3-diamine, N, N'-diethylpropane-1, 3-diamine and / or N, N'-Diisopropylpropan-1 , 3-diamine used.

Als Duftaldehyde können alle üblichen Duftaldehyde eingesetzt werden, die typischerweise zur Herbeiführung eines angenehmen Duftempfindens eingesetzt werden. Geeignete Duftaldehyde sind dem Fachmann bekannt. Geeignete Duftaldehyde können beliebige Aldehyde sein, insbesondere solche, die einen gewünschten Frischeduft oder eine Frischeempfinden vermitteln. Denn dies ist erfindungsgemäß besonders gewünscht, insbesondere mit Blick auf ein besonders intensives und lang anhaltendes Frischeempfinden. Es kann sich um einzelne Aldehyde oder Aldehydgemische handeln. Die Duftaldehyde können insbesondere eine aliphatische, cyclo- aliphatische, aromatische, ethylenisch ungesättigte Struktur oder eine Kombination dieser Strukturen aufweisen. Es können ferner weitere Heteroatome oder polycyclische Strukturen vorliegen. Die Strukturen können geeignete Substituenten wie Hydroxyl- oder Aminogruppen aufweisen. Wenn in dem erfindungsgemäßen Mittel als Komponente (a) ein Duftaldehyd eingesetzt wird, ausgewählt aus Adoxal, Anisaldehyd, Cymal, Ethylvanillin, Florhydral, Helional, Heliotropin, Hydroxycitronellal, Koavon, Lauraldehyd, Lyral, Methylnonylacetaldehyd, P. T. Bucinal, Phenylacetaldehyd, Undecylenaldehyd, Vanillin, 2,6,10-Trimethyl-9-undecenal, 3-Dodecen-1-al, alpha-n-Amylzimtaldehyd, 4-Methoxybenzaldehyd, Benzaldehyd, 3-(4-tert-Butylphenyl)-propanal, 2-Methyl-3-(para-methoxyphenyl)propanal, 2-Methyl-4-(2,6,6-timethyl-2(1 )-cyclohexen-1-yl)butanal, 3-Phenyl-2-propenal, cis-/trans-3,7-Dimethyl- 2,6-octadien-1-al, 3,7-Dimethyl-6-octen-1-al, [(3,7- Dimethyl-6-octenyl)oxy]acetaldehyd, 4-lsopropylbenzyaldehyd, 1 ,2,3,4,5,6,7,8-Octahydro-8,8- dmethyl-2-naphthaldehyd, 2,4-Dimethyl-3-cyclohexen-1-carboxaldehyd, 2-Methyl-3-(isopropyl- phenyl)propanal, 1-Decanal, Decylaldehyd, 2,6-Dimethyl-5-heptenal, 4-(Tricyclo[ 5.2.1.0(2,6)]- decyliden-8)-butanal, Octahydro-4,7-methan-1 H-indencarboxaldehyd, 3-Ethoxy-4- hydroxybenzaldehyd, para-Ethyl-alpha,alphadimethylhydrozimtaldehyd, alpha-Methyl-3,4- (methylendioxy)-hydrozimtaldehyd, 3,4-Methylendioxybenzaldehyd, alpha-n-Hexylzimtaldehyd, m- Cymen-7-carboxaldehyd, alpha-Methylphenylacetaldehyd, 7-Hydroxy-3,7-dimethyloctanal, Undecenal, 2,4,6-Trimethyl-3-cyclohexen-1-carboxaldehyd, 4-(3)(4-Methyl-3-pentenyl)-3- cyclohexencarboxaldehyd, 1-Dodecanal, 2,4-Dimethylcyclohexen-3-carboxaldehyd, 4-(4-Hydroxy- 4-methylpentyl)-3-cylohexen-1-carboxaldehyd, 7-Methoxy-3,7-dimethyloctan-1-al 2-Methylun- decanal, 2-Methyldecanal, 1-Nonanal, 1-Octanal, 2,6,10-Trimethyl-5,9-undecadienal, 2-Methyl- 3- (4-tert-butyl)propanal, Dihydrozimtaldehyd, 1-Methyl-4-(4-methyl-3-pentenyl)-3-cyclohexen-1- carboxaldehyd, 5- oder 6-Methoxyhexahydro-4,7-methanindan-1- oder -2-carboxaldehyd, 3,7- Dimethyloctan-1-al, 1-Undecanal, 10-Undecen-1-al, 4-Hydroxy-3-methoxybenzaldehyd, 1-Methyl- 3-(4-methylpentyl)-3-cyclohexencarboxaldehyd, 7-Hydroxy-3,7-dimethyl-octanal, trans-4-Decenal, 2,6-Nonadienal, para-Tolylacetaldehyd, 4-Methylphenylacetaldehyd, 2-Methyl-4-(2,6,6-trimethyl-1- cyclohexen-1-yl)-2-butenal, ortho-Methoxyzimtaldehyd, S.δ.θ-Trimethyl-S-cyclohexencarbox- aldehyd, 3,7-Dimethyl-2-methylen-6-octenal, Phenoxyacetaldehyd, 5,9-Dimethyl-4,8-decadienal, Päonienaldehyd (6,10-Dimethyl-3-oxa-5,9-undecadien-1-al), Hexahydro- 4,7-methanindan-1-car- boxaldehyd, 2-Methyloctanal, alpha-Methyl-4-(1-methylethyl)benzolacetaldehyd, 6,6-Dimethyl-2- norpinen-2-propionaldehyd, para-Methylphenoxyacetaldehyd, 2-Methyl-3-phenyl-2-propen- 1-al 3,5,5-Trimethylhexanal, Hexahydro-8,8-dimethyl-2-naphthaldehyd, 3-Propylbicyclo[ 2.2.1]-hept-5- en-2-carbaldehyd, 9-Decenal, 3-Methyl-5-phenyl-1-pentanal, Methylnonylacetaldehyd, Hexanal, trans-2-Hexenal, 1-p-Menthen-q-carboxaldehyd oder Mischungen davon, so liegt eine bevorzugte Ausführungsform der Erfindung vor.As fragrance aldehydes, it is possible to use all customary fragrant aldehydes which are typically used to produce a pleasant scent sensation. Suitable fragrance aldehydes are known to the person skilled in the art. Suitable fragrance aldehydes may be any aldehydes, especially those which impart a desired fresh scent or sensation of freshness. Because this is particularly desirable according to the invention, especially with a view to a particularly intense and long-lasting feeling of freshness. It may be individual aldehydes or aldehyde mixtures. The fragrance aldehydes may in particular have an aliphatic, cycloaliphatic, aromatic, ethylenically unsaturated structure or a combination of these structures. There may also be other heteroatoms or polycyclic structures. The structures may have suitable substituents such as hydroxyl or amino groups. When in the agent according to the invention as component (a) a fragrance aldehyde is used, selected from Adoxal, Anisaldehyd, Cymal, Ethylvanillin, Florhydral, Helional, Heliotropin, Hydroxycitronellal, Koavon, Lauraldehyd, Lyral, Methylnonylacetaldehyd, PT Bucinal, Phenylacetaldehyd, Undecylenaldehyd, Vanillin, 2,6,10-trimethyl-9-undecenal, 3-dodecene-1-al, alpha-n-amyl-cinnamic aldehyde, 4-methoxybenzaldehyde, benzaldehyde, 3- (4-tert-butylphenyl) -propanal, 2-methyl-3- (para-methoxyphenyl) propanal, 2-methyl-4- (2,6,6-timethyl-2 (1) -cyclohexen-1-yl) butanal, 3-phenyl-2-propenal, cis- / trans-3, 7-dimethyl-2,6-octadiene-1-al, 3,7-dimethyl-6-octene-1-al, [(3,7-dimethyl-6-octenyl) oxy] acetaldehyde, 4-isopropylbenzaldehyde, 1, 2,3,4,5,6,7,8-octahydro-8,8-dimethyl-2-naphthaldehyde, 2,4-dimethyl-3-cyclohexene-1-carboxaldehyde, 2-methyl-3- (isopropyl-phenyl ) propanal, 1-decanal, decyl aldehyde, 2,6-dimethyl-5-heptenal, 4- (tricyclo [5.2.1.0 (2,6)] decylidene-8) -butanal, octahydro-4,7-methane-1 H-indenecarboxaldehyde, 3 -Ethoxy-4-hydroxybenzaldehyde, para-ethyl-alpha, alphadimethylhydrocinnamaldehyde, alpha-methyl-3,4- (methylenedioxy) -hydrocinnamaldehyde, 3,4-methylenedioxybenzaldehyde, alpha-n-hexylcinnamaldehyde, m-cymene-7-carboxaldehyde, alpha Methylphenylacetaldehyde, 7-hydroxy-3,7-dimethyloctanal, undecenal, 2,4,6-trimethyl-3-cyclohexene-1-carboxaldehyde, 4- (3) (4-methyl-3-pentenyl) -3-cyclohexenecarboxaldehyde, 1-dodecanal, 2,4-dimethylcyclohexene-3-carboxaldehyde, 4- (4-hydroxy-4-methylpentyl) -3-cyclohexene-1-carboxaldehyde, 7-methoxy-3,7-dimethyloctan-1-al 2-methylun decanal, 2-methyldecanal, 1-nonanal, 1-octanal, 2,6,10-trimethyl-5,9-undecadienal, 2-methyl-3- (4-tert-butyl) propanal, dihydrocinnamaldehyde, 1-methyl 4- (4-methyl-3-pentenyl) -3-cyclohexene-1-carboxaldehyde, 5- or 6-methoxy-hexahydro-4,7-methanindan-1 or 2-carboxaldehyde, 3,7-dimethyloctan-1-al , 1-undecanal, 10-undecene-1-al, 4-hydroxy-3-methoxybenzaldehyde, 1-methyl-3- (4-methylpentyl) -3-cyclohexenecarboxaldehyde, 7-hydroxy-3,7-dimethyl-octanal, trans -4- Decenal, 2,6-nonadienal, para-tolylacetaldehyde, 4-methylphenylacetaldehyde, 2-methyl-4- (2,6,6-trimethyl-1-cyclohexen-1-yl) -2-butenal, ortho-methoxycinnamaldehyde, S. δ, θ-trimethyl-S-cyclohexene-carboxaldehyde, 3,7-dimethyl-2-methylene-6-octenal, phenoxyacetaldehyde, 5,9-dimethyl-4,8-decadienal, peonyaldehyde (6,10-dimethyl-3-) oxa-5,9-undecadiene-1-al), hexahydro-4,7-methanindane-1-carboxaldehyde, 2-methyloctanal, alpha-methyl-4- (1-methylethyl) benzeneacetaldehyde, 6,6-dimethyl 2-norpinen-2-propionaldehyde, para-methylphenoxyacetaldehyde, 2-methyl-3-phenyl-2-propene-1-al 3,5,5-trimethylhexanal, hexahydro-8,8-dimethyl-2-naphthaldehyde, 3-propylbicyclo [2.2.1] hept-5-ene-2-carbaldehyde, 9-decenal, 3-methyl-5-phenyl-1-pentanal, methylnonylacetaldehyde, hexanal, trans-2-hexenal, 1-p-menthene-q- carboxaldehyde or mixtures thereof, so is a preferred embodiment of the invention.

Weiterhin ist es im Sinne der Erfindung vorteilhaft, zusätzlich zum Duftaldehyd auch Duftketone einzusetzen. Eine bevorzugte Ausführungsform der Erfindung liegt daher vor, wenn zusätzlich zumindest ein Duftketon eingesetzt wird, insbesondere ausgewählt aus Buccoxim; iso-Jasmon; Methyl-beta-naphthylketon; Moschusindanon; Tonalid/Musk plus; alpha-Damascon, beta- Damascon, delta-Damascon, iso-Damascon, Damascenon, Damarose, Methyldihydrojasmonat, Menthon, Carvon, Kampfer, Fenchon, alpha-lonon, beta-lonon, gamma-Methyl ge-nannt lonon, Fleuramon, Dihydrojasmon, cis-Jasmon, iso-E-Super®, Methylcedrenylketon oder Methylcedry-Ion, Acetophenon, Methylacetophenon, para-Methoxyacetophenon, Methyl-beta-naphtylketon, Benzylaceton, Benzophenon, para-Hydroxyphenylbutanon, Sellerie-Keton oder Livescone, 6- lsopropyldecahydro-2-naphton, Dimethyloctenon, Frescomenthe, 4-(1-Ethoxyvinyl)-3, 3,5,5- tetramethylcyclohexanon, Methylheptenon, 2-(2-(4-Methyl-3-cyclohexen-1-yl)propyl)cyclopentanon, 1-(p-Menthen-6(2)yl)-1-propanon, 4-(4-Hydro-xy-3-methoxyphenyl)-2-butanon, 2-Acetyl-3,3- dimethylnorbornan, 6,7-Dihydro-1 ,1 ,2,3,3-pentamethyl-4(5H)in-danon, 4-Damascol, Dulcinyl oder Cassion, Gelson, Hexalon, lsocyclemon E, Methylcyclocitron, Methyllavendelketon, Orivon, para- tertiärem Butylcyclohexanon, Verdon, Delphon, Muscon, Neobutenon, Plicaton, Velou-ton, 2,4,4,7- Tetramethyl-oct-6-en-3-on, Tetrameran oder Mischungen davon. Bevorzugt können die Ketone ausgewählt sein aus Alpha Damascon, Delta Damascon, Iso Damascon, Carvon, Gamma-Methyl- ionon, Iso-E-Super, 2,4,4,7-Tetramethyl-oct-6-en-3-on, Benzylaceton, Beta Damascon, Damascenon, Methyldihydrojasmonat, Methyl-cedrylon, Hedion und Gemischen davon.Furthermore, it is advantageous in the context of the invention to use fragrance ketones in addition to the fragrance aldehyde. A preferred embodiment of the invention is therefore present if in addition at least one fragrance ketone is used, in particular selected from buccoxime; iso-jasmone; Methyl-beta-naphthyl ketone; musk indanone; Tonalid / Musk plus; alpha damascone, beta Damascone, delta-damascon, iso-damascon, damascenon, damarose, methyldihydrojasmonate, menthone, carvone, camphor, fenchone, alpha-ionone, beta-ionone, gamma-methyl called lonon, fleuramon, dihydrojasmon, cis-jasmone, iso- E-Super®, methyl cedryl ketone or methyl citrate ion, acetophenone, methyl acetophenone, para-methoxy acetophenone, methyl beta-naphthyl ketone, benzyl acetone, benzophenone, para-hydroxyphenyl butanone, celery ketone or live scone, 6-isopropyl decahydro-2-naphthone, dimethyloctenone, Frescomenthe , 4- (1-Ethoxy-vinyl) -3,3,5,5-tetramethylcyclohexanone, methylheptenone, 2- (2- (4-methyl-3-cyclohexen-1-yl) -propyl) -cyclopentanone, 1- (p-menthene) 6 (2) yl) -1-propanone, 4- (4-hydroxy-3-methoxyphenyl) -2-butanone, 2-acetyl-3,3-dimethylnorbornane, 6,7-dihydro-1, 1, 2 , 3,3-pentamethyl-4 (5H) in-danone, 4-damascol, dulcinyl or cassion, gelson, hexalon, isocyclone E, methylcyclocitron, methyllavedelketone, orivone, para-tertiary butylcyclohexanone, verdone, delphone, muscone, neobutenone, plicaton , Velou-ton, 2,4,4,7 Tetramethyl-oct-6-en-3-one, tetrameran or mixtures thereof. Preferably, the ketones may be selected from Alpha Damascon, Delta Damascone, Iso Damascone, Carvon, gamma-methyl ionone, Iso-E-Super, 2,4,4,7-tetramethyl-oct-6-en-3-one, Benzylacetone, Beta Damascone, Damascenone, methyl dihydrojasmonate, methyl cedrylon, hedione and mixtures thereof.

Für weitere geeignete Duftstoffe, ausgewählt aus Aldehyden und Ketonen, wird auf Steffen Arctander Published 1960 and 1969 respectively, Reprinted 2000 ISBN: Aroma Chemicals Vol. 1 : 0-931710-37-5, Aroma Chemicals Vol. 2: 0-931710-38-3, verwiesen.For other suitable fragrances selected from aldehydes and ketones, see Steffen Arctander Published 1960 and 1969, respectively, Reprinted 2000 ISBN: Aroma Chemicals Vol. 1: 0-931710-37-5, Aroma Chemicals Vol. 2: 0-931710-38 -3, referenced.

In einer weiteren bevorzugten Ausführungsform der Erfindung ist die Komponente (b) in Mengen von 0,001 Gew.-% bis 3 Gew.-%, vorzugsweise 0,01 bis 2 Gew.-%, insbesondere 0,1 bis 1 Gew.- % in dem Mittel enthalten, bezogen auf das gesamte Mittel. Auf diese Weise sind besonders gute Duftresultate im Sinne der Erfindung realisierbar. Wenn ein erfindungsgemäßes Mittel 0,001 Gew.- % bis 3 Gew.-%, vorzugsweise 0,01 bis 2 Gew.-%, insbesondere 0,1 bis 1 Gew.-% Duftaldehyde enthält, Gew.-% bezogen auf das gesamte Mittel, so liegt ebenfalls eine bevorzugte Ausführungsform der Erfindung vor. So sind ebenfalls besonders gute Duftresultate im Sinne der Erfindung darstellbar. Insbesondere ist es für die Erzielung besonders guter Duftresultate vorteilhaft, wenn das Verhältnis von Komponente (a) zu Komponente (b) 25:1 bis 1 :5 beträgt. Dann liegt wiederum eine bevorzugte Ausführungsform der Erfindung vor.In a further preferred embodiment of the invention, the component (b) in amounts of 0.001 wt .-% to 3 wt .-%, preferably 0.01 to 2 wt .-%, in particular 0.1 to 1 wt .-% in the mean, based on the total In this way, particularly good scent results within the meaning of the invention can be realized. If an agent according to the invention contains 0.001% by weight to 3% by weight, preferably 0.01% to 2% by weight, in particular 0.1% to 1% by weight, of fragrance aldehydes,% by weight, based on the total agent, so is also a preferred embodiment of the invention. Thus, also very good scent results within the meaning of the invention can be represented. In particular, it is advantageous for achieving particularly good scent results if the ratio of component (a) to component (b) is 25: 1 to 1: 5. Then again there is a preferred embodiment of the invention.

Weiterhin ist es bevorzugt, dass die gesamte Riechstoffmenge des Mittels, umfassend also auch alle enthaltenen Duftaldehyde, 0,01 bis 10 Gew.-%, vorzugsweise 0,1 bis 5 Gew.-%, insbesondere 0,3 bis 3 Gew.-% beträgt. Dies entspricht einer bevorzugten Ausführungsform der Erfindung.Furthermore, it is preferred that the total amount of fragrance of the agent, including all fragrance aldehydes contained, 0.01 to 10 wt .-%, preferably 0.1 to 5 wt .-%, in particular 0.3 to 3 wt .-% is. This corresponds to a preferred embodiment of the invention.

Gemäß einer weiteren bevorzugten Ausführungsform der Erfindung liegt das erfindungsgemäße Mittel in fester Form vor, vorzugsweise in Pulverform oder auch in Granulatform oder in Gestalt von Pressformkörpern, Z.B. Tabletten. Es ist aber auch möglich, dass das erfindungsgemäße Mittel in flüssiger Form vorliegt, vorzugsweise in Gelform. Auch dies entspricht einer bevorzugten Ausführungsform der Erfindung.According to a further preferred embodiment of the invention, the agent according to the invention is in solid form, preferably in powder form or else in granular form or in the form of molded articles, for example tablets. But it is also possible that the inventive agent in in liquid form, preferably in gel form. This, too, corresponds to a preferred embodiment of the invention.

Neben den Duftaldehyden und dem (ggf. substituierte) Ethylendiamin und/oder (ggf. substituierte) Propylendiamin kann das erfindungsgemäße Mittel weitere geeignete Inhaltsstoffe umfassen, insbesondere aber Tenside. Wenn das erfindungsgemäße Mittel zumindest 5 Gew.-%, vorzugsweise zumindest 8 Gew.-%, insbesondere zumindest 10 Gew.-% Tensid enthält, insbesondere Aniontensid und/oder Niotensid, so liegt eine bevorzugte Ausführungsform der Erfindung vor. Eine sinnvolle Obergrenze für Tensid kann z.B. bei 40 Gew.-% oder 30 Gew.-% oder 20 Gew.-% liegen, Gew.-% jeweils bezogen auf das gesamte Mittel. Tenside werden weiter unten noch genauer beschrieben.In addition to the fragrance aldehydes and the (optionally substituted) ethylenediamine and / or (optionally substituted) propylenediamine, the composition according to the invention may comprise further suitable ingredients, but in particular surfactants. If the agent according to the invention contains at least 5% by weight, preferably at least 8% by weight, in particular at least 10% by weight of surfactant, in particular anionic surfactant and / or nonionic surfactant, then a preferred embodiment of the invention is present. A reasonable upper limit for surfactant may e.g. at 40 wt .-% or 30 wt .-% or 20 wt .-%, wt .-% in each case based on the total mean. Surfactants will be described in more detail below.

Ein weiterer Gegenstand der Erfindung ist ein Textilreinigungs- oder konditionierverfahren, bei welchem das zu reinigende Textil einer Textilwäsche unter Einsatz eines erfindungsgemäßen Wasch-, Reinigungs- oder Pflegemittels unterworfen wird, insbesondere in einer automatischen Waschmaschine, vorzugsweise bei Temperaturen nicht über 6O0C, insbesondere nicht über 4O0C.Another object of the invention is a textile cleaning or conditioning process in which the textile to be cleaned is subjected to textile washing using a washing, cleaning or care agent according to the invention, in particular in an automatic washing machine, preferably at temperatures above 6O 0 C, in particular not 4O 0 C.

Ein weiterer Gegenstand der Erfindung liegt auch in der Verwendung eines erfindungsgemäßen Wasch-, Reinigungs- oder Pflegemittels zum Reinigen und/oder Konditionieren von textilen Flächengebilden, insbesondere in einer automatischen Waschmaschine, vorzugsweise bei Temperaturen nicht über 6O0C, insbesondere nicht über 4O0C.Another object of the invention is the use of a washing, cleaning or care agent according to the invention for cleaning and / or conditioning of textile fabrics, in particular in an automatic washing machine, preferably at temperatures not above 6O 0 C, in particular not above 40 0 C. ,

Ein weiterer Gegenstand der Erfindung liegt in der Verwendung von (ggf. substituiertem) Ethylendiamin und/oder (ggf. substituiertem) Propylendiamin als separat zugegebene Komponente in riechstoff haltigen Wasch-, Reinigungs- oder Pflegemitteln, welche Duftstoffaldehyd enthalten, zur Verlängerung der Duftwirkung des Wasch-, Reinigungs- oder Pflegemittels. „Separat zugegebene Komponente" bezieht sich hierbei auf die ebenfalls enthaltenen Duftaldehyde und soll bedeuten, dass Ethylendiamin und/oder (ggf. substituiertem) Propylendiamin sowie die Duftaldehyde als gesonderte Entitäten in das Wasch-, Reinigungs- oder Pflegemittel eingehen. Es ist z.B. auch möglich, die Komponenten (a) und (b) in einem einzigen Schritt in das Produkt einzubringen, z.B. zusammen mit der übrigen Parfümierung, sofern die Komponenten (a) und (b) bei der Zugabe getrennt vorliegen, z.B. als separate Komponenten eines Parfümöls.Another object of the invention is the use of (optionally substituted) ethylenediamine and / or (optionally substituted) propylenediamine as a separately added component in perfume-containing detergents, cleaning or care products containing fragrance aldehyde, to extend the fragrance effect of the wash , Cleaning or care products. "Separately added component" here refers to the fragrance aldehydes likewise contained and is intended to mean that ethylenediamine and / or (optionally substituted) propylenediamine and fragrance aldehydes enter the washing, cleaning or care agent as separate entities to introduce the components (a) and (b) into the product in a single step, eg together with the rest of the perfuming, provided that the components (a) and (b) are present separately during the addition, for example as separate components of a perfume oil.

Ein weiterer Gegenstand der Erfindung liegt in der Verwendung von (ggf. substituiertem) Ethylendiamin und/oder (ggf. substituiertem) Propylendiamin als separat zugegebene Komponente in riechstoffhaltigen Wasch-, Reinigungs- oder Pflegemitteln, welche Duftstoffaldehyd enthalten, zur Erzielung eines lange anhaltenden Frischegeruches bei der Anwendung des Wasch-, Reinigungs- oder Pflegemittels. „Separat zugegebene Komponente" ist hierbei wie zuvor beschrieben zu verstehen.Another object of the invention is the use of (optionally substituted) ethylenediamine and / or (optionally substituted) propylenediamine as a separately added component in perfume-containing detergents, cleaning or care products containing fragrance aldehyde, to achieve a long-lasting fresh smell at the application of the washing, Cleaning or care products. "Separately added component" is to be understood as previously described.

Bei dem Wasch-, Reinigungs- oder Pflegemittel kann es sich insbesondere um ein Textilbehandlungsmittel in Form eines Textilwaschmittels, Weichspülers, weichmachenden Waschmittels oder Waschhilfsmittels handeln. Ebenso kann es sich z.B. um ein Reinigungsmittel für harte Oberflächen handeln, wie vorzugsweise um ein Geschirrspülmittel, insbesondere um ein maschinelles Geschirrspülmittel. Ebenso kann es sich um Reinigungsmittel wie z.B. Haushaltsreiniger, Allzweckreiniger, Fensterreiniger, Fußbodenreiniger usw. handeln. Vorzugsweise kann es sich um einThe washing, cleaning or care agent may in particular be a textile treatment agent in the form of a textile detergent, fabric conditioner, softening detergent or washing aid. It may also be e.g. to be a hard surface cleaning agent, such as preferably a dishwashing detergent, especially a machine dishwashing detergent. It may also be detergents, e.g. Household cleaners, all-purpose cleaners, window cleaners, floor cleaners, etc. act. Preferably, it may be a

Produkt zur Reinigung von WC-Becken und Urinalen handeln, vorteilhafterweise um einen Spülreiniger zum Einhängen in das WC-Becken oder den Spülkasten, insbesondere um einen sogenannten WC-Stein. Im Sinne des Pflegemittels handelt es sich bevorzugt um Kosmetika, wie z.B. Haarshampoos, Deos usw., welche für die Körperpflege und/oder -reinigung einsetzbar sind. Im Sinne des Pflegemittels kann es sich ferner auch um Air-Care-Produkte und Raumluftverbesserer handeln.Product for cleaning toilet bowls and Urinalen act, advantageously a flushing cleaner for hanging in the toilet bowl or the cistern, especially around a so-called toilet block. The care agent is preferably cosmetics, e.g. Hair shampoos, deodorants, etc., which can be used for personal care and / or cleaning. The care product may also be air care products and room air improvers.

Gemäß einer bevorzugten Ausführungsform handelt es sich bei dem erfindungsgemäßen Mittel daher um ein Textilbehandlungsmittel, ein Bügelhilfsmittel, ein Reinigungstuch, ein Textilwaschmittel, einen Weichspüler, ein Reinigungsmittel, insbesondere für harte und/oder weiche Oberflächen, einen Haushaltsreiniger, ein Pflegemittel, ein Waschpflegemittel, ein Raumbe- duftungsmittel, einen Luftverbesserer, ein Konditioniermittel, ein Färbemittel, einen Weichspüler, ein Konditioniersubstrat, ein Putzmittel, ein kosmetisches Mittel, ein Bleichmittel, ein Entkalkungsmittel, ein Autopflegemittel, Fußbodenpflegemittel, Herdpflegemittel, Lederpflegemittel, Möbelpflegemittel, ein Scheuermittel, ein Desinfektionsmittel, ein Beduftungsmittel, ein Schimmelentfernungsmittel und/oder ein Vorprodukt der vorgenannten Mittel. Es ist ein Vorteil der Erfindung, dass die erfindungsgemäßen Mittel sehr lagerstabil sind.According to a preferred embodiment, the agent according to the invention is therefore a textile treatment agent, an ironing aid, a cleaning cloth, a laundry detergent, a softener, a cleaning agent, in particular for hard and / or soft surfaces, a household cleaner, a care agent, a laundry care product Room fragrancing agent, an air freshener, a conditioning agent, a coloring agent, a fabric softener, a conditioning substrate, a cleaning agent, a cosmetic, a bleach, a descaling agent, a car care product, floor care products, stoves, leather care products, furniture care products, a scouring agent, a disinfectant Scenting agent, a mold remover and / or a precursor of the aforementioned means. It is an advantage of the invention that the agents according to the invention are very stable on storage.

Nach einer weiteren bevorzugten Ausführungsform der Erfindung sind in dem erfindungsgemäßen Mittel zusätzliche(n) Duftstoff(e) enthalten, insbesondere ausgewählt aus der Gruppe umfassend Duftstoffe natürlichen oder synthetischen Ursprungs, bevorzugt leichter flüchtige Duftstoffe, höhersiedende Duftstoffe, feste Duftstoffe und/oder haftfeste Duftstoffe.According to a further preferred embodiment of the invention, the composition according to the invention contains additional fragrance (s), in particular selected from the group consisting of fragrances of natural or synthetic origin, preferably more volatile fragrances, higher-boiling fragrances, solid fragrances and / or strong fragrances.

Haftfeste Riechstoffe, die im Rahmen der vorliegenden Erfindung mit Vorteil einsetzbar sind, sind beispielsweise etherische Öle wie Angelikawurzelöl, Anisöl, Arnikablütenöl, Basilikumöl, Bayöl, Bergamottöl, Champacablütenöl, Edeltannenöl, Edeltannenzapfenöl, Elemiöl, Eukalyptusöl, Fenchelöl, Fichtennandelöl, Galbanumöl, Geraniumöl, Gingergrasöl, Guajakholzöl, Gurjunbalsamöl, Helichrysumöl, Ho-Öl, Ingweröl, Irisöl, Kajeputöl, Kalmusöl, Kamillenöl, Kampferöl, Kanagaöl, Kardamomenöl, Kassiaöl, Kiefernnadelöl, Kopaivabalsamöl, Korianderöl, Krauseminzeöl, Kümmelöl, Kuminöl, Lavendelöl, Lemon-grasöl, Limetteöl, Mandarinenöl, Melissenöl, Moschuskörneröl, Myrrhenöl, Nelkenöl, Neroliöl, Niaouliöl, Olibanumöl, Orangenöl, Origanumöl, Palmarosaöl, Patschuliöl, Perubalsamöl, Petitgrainöl, Pfefferöl, Pfefferminzöl, Pimentöl, Pine-Öl, Rosenöl, Rosmarinöl, Sandelholzöl, Sellerieöl, Spiköl, Sternanisöl, Terpentinöl, Thujaöl, Thymianöl, Verbenaöl, Vetiveröl, Wacholderbeeröl, Wermutöl, Wintergrünöl, Ylang-Ylang- Öl, Ysop-Öl, Zimtöl, Zimtblätteröl, Zitronellöl, Zitronenöl sowie Zypressenöl.Adherent fragrances which are advantageously used in the present invention are, for example, essential oils such as angelica root oil, aniseed oil, arnica blossom oil, basil oil, bay oil, bergamot oil, Champacablütenöl, Edeltannöl, Edeltannenzapfen oil, Elemiöl, eucalyptus oil, fennel oil, spruce oil, galbanum oil, geranium oil, gingergrass oil , Guaiac wood oil, gurdy balm oil, helichrysum oil, ho oil, ginger oil, iris oil, cajeput oil, calamus oil, chamomile oil, Camphor oil, kanga oil, cardamom oil, cassia oil, pine oil, copaiba balsam, coriander oil, spearmint oil, caraway oil, cumin oil, lavender oil, lemon grass oil, lime oil, tangerine oil, lemon balm oil, musk kernel oil, myrrh oil, clove oil, neroli oil, niaouli oil, olibanum oil, orange oil, origanum oil, palmarosa oil, Patchouli oil, Peruvian balsam oil, Petitgrain oil, Pepper oil, Peppermint oil, Pimento oil, Pine oil, Rose oil, Rosemary oil, Sandalwood oil, Celery oil, Spik oil, Star aniseed oil, Turpentine oil, Thuja oil, Thyme oil, Verbena oil, Vetiver oil, Juniper berry oil, Vermouth oil, Wintergreen oil, Ylang-ylang oil, Hyssop oil, cinnamon oil, cinnamon oil, lemon oil, lemon oil and cypress oil.

Aber auch höhersiedende bzw. feste Riechstoffe natürlichen oder synthetischen Ursprungs können im Rahmen der vorliegenden Erfindung als haftfeste Riechstoffe bzw. Riechstoffgemische, also Duftstoffe eingesetzt werden. Zu diesen Verbindungen zählen die nachfolgend genannten Verbindungen sowie Mischungen aus diesen: Ambrettolid, α-Amylzimtaldehyd, Anethol, Anisaldehyd, Anisalkohol, Anisol, Anthranilsäuremethylester, Acetophenon, Benzylaceton, Benzaldehyd, Benzoesäureethylester, Benzophenon, Benzylalkohol, Benzylacetat, Benzylbenzoat, Benzylformiat, Benzylvalerianat, Borneol, Bornylacetat, α-Bromstyrol, n-Decylaldehyd, n- Dodecylalde-hyd, Eugenof, Eugenolmethylether, Eukalyptol, Farnesol, Fenchon, Fenchylacetat, Geranylacetat, Geranylformiat, Heliotropin, Heptincarbonsäuremethylester, Heptaldehyd, Hy- drochinon- Dimethylether, Hydroxyzimtaldehyd, Hydroxyzimtalkohol, Indol, Iron, Isoeugenol, Isoeugenolmethylether, Isosafrol, Jasmon, Kampfer, Karvakrol, Karvon, p-Kresol-methylether, Cumarin, p-Methoxyacetophenon, Methyl-n-amylketon, Methylanthranil-säure-methylester, p- Methylacetophenon, Methylchavikol, p-Methylchinolin, Methyl-ß-naphthylketon, Methyl-n- nonylacetaldehyd, Methyl-n-nonylketon, Muskon, ß-Naphtholethylether, ß-Naphtholmethylether, Nerol, Nitrobenzol, n-Nonylaldehyd, Nonylakohol, n-Octylaldehyd, p-Oxy-Acetophenon, Pentadekanolid, ß-Phenylethylalkohol, Phenylacetaldehyd-Dimethylacetal, Phenylessigsäure, Pulegon, Safrol, Salicylsäureisoamylester, Salicylsäuremethylester, Salicylsäurehexylester, Salicyl- säurecyclohexylester, Santalol, Skatol, Terpineol, Thymen, Thymol, γ-Undelacton, Vanilin, Veratrumaldehyd, Zimtaldehyd, Zimatalkohol, Zimtsäure, Zimtsäureethylester, Zimtsäurebenzylester. Zu den leichter flüchtigen Duftstoffen zählen insbesondere die niedriger siedenden Riechstoffe natürlichen oder synthetischen Ursprung, die allein oder in Mischungen eingesetzt werden können. Beispiele für leichter flüchtige Duftstoffe sind Alkylisothiocyanate (Alkylsenföle), Butandion, Limonen, Linalool, Linaylacetat und -Propionat, Menthol, Menthon, Methyl-n-heptenon, Phellandren, Phenylacetaldehyd, Terpinylacetat, Zitral, Zitronellal.But also higher-boiling or solid fragrances of natural or synthetic origin can be used in the context of the present invention as adherent fragrances or fragrance mixtures, ie fragrances. These compounds include the following compounds and mixtures thereof: ambrettolide, α-amylcinnamaldehyde, anethole, anisaldehyde, anisalcohol, anisole, methyl anthranilate, acetophenone, benzylacetone, benzaldehyde, ethyl benzoate, benzophenone, benzyl alcohol, benzyl acetate, benzyl benzoate, benzyl formate, benzyl valerate, borneol , Bornyl acetate, α-bromostyrene, n-decyl aldehyde, n-dodecyl aldehyde, Eugenof, eugenol methyl ether, eucalyptol, farnesol, fenchone, fenchyl acetate, geranyl acetate, geranyl formate, heliotropin, heptincarboxylic acid methyl ester, heptaldehyde, hydroquinone dimethyl ether, hydroxycinnamaldehyde, hydroxycinnamyl alcohol, indole , Iron, isoeugenol, isoeugenol methyl ether, isosafrole, jasmone, camphor, Karvakrol, Karvon, p-cresol methyl ether, coumarin, p-methoxyacetophenone, methyl n-amyl ketone, methyl anthraniloic acid methyl ester, p-methylacetophenone, methylchavikole, p-methylquinoline , Methyl β-naphthyl ketone, methyl n-nonyl acetaldehyde, methyl n-nonyl ketone, Mu β-naphthol ethyl ether, β-naphthol methyl ether, nerol, nitrobenzene, n-nonyl aldehyde, nonyl alcohol, n-octyl aldehyde, p-oxyacetophenone, pentadecanolide, β-phenylethyl alcohol, phenyl acetaldehyde dimethyl acetal, phenylacetic acid, pulegone, safrole, salicylic acid isoamyl ester, methyl salicylate, Salicylic acid hexyl ester, cyclohexyl salicylate, santalol, skatole, terpineol, thymes, thymol, γ-undelactone, vaniline, veratrum aldehyde, cinnamaldehyde, cimat alcohol, cinnamic acid, cinnamic acid ethyl ester, cinnamic acid benzyl ester. The more volatile fragrances include, in particular, the lower-boiling fragrances of natural or synthetic origin, which can be used alone or in mixtures. Examples of more volatile fragrances are alkyl isothiocyanates (alkylmustard oils), butanedione, limonene, linalool, linayl acetate and propionate, menthol, menthone, methyl-n-heptenone, phellandrene, phenylacetaldehyde, terpinyl acetate, citral, citronellal.

Zur beschleunigten oder verzögerten Freisetzung von Duftstoffen können alle im Stand der Technik bekannten Verfahren angewendet werden, soweit sie dem Fachmann als geeignet erscheinen. Gemäß einer bevorzugten Ausführungsform der Erfindung umfasst das erfindungsgemäße Mittel geträgerten und/oder verkapselten Duftstoff. Nach einer weiteren bevorzugten Ausführungsform weist das erfindungsgemäße Wasch-, Pflegeoder Reinigungsmittel, wenigstens eine, vorzugsweise mehrere, aktive Komponenten, insbesondere wasch-, pflege-, reinigungsaktive und/oder kosmetische Komponenten auf, vorteilhafterweise ausgewählt aus der Gruppe umfassend anionische Tenside, kationische Tenside, amphotere Tenside, nichtionische Tenside, Acidifizierungsmittel, Alkalisierungsmittel, Anti-Knitter-Verbindungen, antibakterielle Stoffe, Antioxidantien, Antiredepositionsmittel, Antistatika, Buildersubstanzen, Bleichmittel, Bleichaktivatoren, Bleichstabilisatoren, Bleichkatalysatoren, Bügelhilfsmittel, Cobuilder, Duftstoffe, Einlaufverhinderer, Elektrolyt^, Enzyme, Farbschutzstoffe, Färbemittel, Farbstoffe, Farbübertragungsinhibitoren, Fluoreszensmittel, Fungizide, Germizide, geruchskomplexierende Substanzen, Hilfsmittel, Hydrotrope, Klarspüler, Komplexbildner, Konservierungsmittel, Korrosionsinhibitoren, wassermischbare organische Lösungsmittel, optische Aufheller, Parfüme, Parfümträger, Perlglanzgeber, pH-Stellmittel, Phobier- und Imprägniermittel, Polymere, Quell- und Schiebefestmittel, Schauminhibitoren, Schichtsilikate, schmutzabweisende Stoffe, Silberschutzmittel, Silikonöle, Soilrelease-Wirkstoffe, UV-Schutz-Substanzen, Viskositätsregulatoren, Verdickungsmittel, Verfärbungsinhibitoren, Vergrauungsinhibitoren, Vitamine und/oder Weichspüler. Im Sinne dieser Erfindung beziehen sich Angaben für das erfindungsgemäße Mittel in Gew.-%, wenn nicht anders angegeben, auf das Gesamtgewicht des erfindungsgemäßen Mittels.For the accelerated or delayed release of perfumes, it is possible to use all processes known in the prior art, insofar as they appear to be suitable for the person skilled in the art. According to a preferred embodiment of the invention, the agent according to the invention comprises supported and / or encapsulated perfume. According to a further preferred embodiment, the washing, care or cleaning agent according to the invention comprises at least one, preferably several, active components, in particular washing, care, cleaning and / or cosmetic components, advantageously selected from the group comprising anionic surfactants, cationic surfactants, amphoteric surfactants, nonionic surfactants, acidifying agents, alkalizing agents, anti-wrinkling compounds, antibacterial agents, antioxidants, anti redeposition agents, antistatic agents, builders, bleaches, bleach activators, bleach stabilizers, bleach catalysts, ironing aids, cobuilders, fragrances, anti-shrinkage agents, electrolyte, enzymes, colorants, Colorants, dyes, color transfer inhibitors, fluorescers, fungicides, germicides, odor-complexing agents, adjuvants, hydrotropes, rinse aids, chelating agents, preservatives, corrosion inhibitors, water-miscible organic Solvents, optical brighteners, perfumes, perfume carriers, pearlescers, pH adjusters, repellents and impregnating agents, polymers, swelling and anti-slip agents, foam inhibitors, phyllosilicates, stain-proofing agents, silver protectants, silicone oils, soil release agents, UV protectants, viscosity regulators, Thickeners, discoloration inhibitors, grayness inhibitors, vitamins and / or fabric softeners. For the purposes of this invention, data for the agent according to the invention in% by weight, unless otherwise stated, relate to the total weight of the composition according to the invention.

Die Mengen der einzelnen Inhaltsstoffe in den erfindungsgemäßen Mitteln orientieren sich jeweils am Einsatzzweck der betreffenden Mittel und der Fachmann ist mit den Größenordnungen der einzusetzenden Mengen der Inhaltsstoffe vertraut oder kann diese der zugehörigen Fachliteratur entnehmen. Je nach Einsatzzweck der erfindungsgemäßen Mittel wird man beispielsweise den Tensidgehalt höher oder niedriger wählen. Üblicherweise kann z. B. der Tensidgehalt beispielsweise von Waschmitteln zwischen 10 und 50 Gew.-%, vorzugsweise zwischen 12,5 und 30 Gew.-% und insbesondere zwischen 15 und 25 Gew.-% betragen, während Reinigungsmittel für das maschinelle Geschirrspülen z.B. zwischen 0,1 und 10 Gew.-%, vorzugsweise zwischen 0,5 und 7,5 Gew.-% und insbesondere zwischen 1 und 5 Gew.-% Tenside enthalten können.The amounts of the individual ingredients in the compositions according to the invention are in each case based on the intended use of the agent in question, and the person skilled in the art is familiar with the orders of magnitude of the ingredients to be used or can refer to these from the associated specialist literature. Depending on the intended use of the compositions according to the invention, for example, the surfactant content will be higher or lower. Usually z. For example, the surfactant content of, for example, detergents is between 10 and 50% by weight, preferably between 12.5 and 30% by weight, and more preferably between 15 and 25% by weight, while automatic dishwashing detergents e.g. between 0.1 and 10 wt .-%, preferably between 0.5 and 7.5 wt .-% and in particular between 1 and 5 wt .-% surfactants may contain.

Die erfindungsgemäßen Mittel können Tenside enthalten, wobei bevorzugt anionische Tenside, nichtionische Tenside und deren Gemische, aber auch kationische Tenside in Frage kommen. Geeignete nichtionische Tenside sind insbesondere Ethoxylierungs- und/oder Propoxylierungs- produkte von Alkylglykosiden und/oder linearen oder verzweigten Alkoholen mit jeweils 12 bis 18 C-Atomen im Alkylteil und 3 bis 20, vorzugsweise 4 bis 10 Alkylethergruppen. Weiterhin sind entsprechende Ethoxylierungs- und/oder Propoxylierungsprodukte von N-Alkylaminen, vicinalen Diolen, Fettsäureestern und Fettsäureamiden, die hinsichtlich des Alkylteils den genannten lang- kettigen Alkoholderivaten entsprechen, sowie von Alkylphenolen mit 5 bis 12 C-Atomen im Alkyl- rest brauchbar. Geeignete anionische Tenside sind insbesondere Seifen und solche, die Sulfat- oder Sulfonat- Gruppen mit bevorzugt Alkaliionen als Kationen enthalten. Verwendbare Seifen sind bevorzugt die Alkalisalze der gesättigten oder ungesättigten Fettsäuren mit 12 bis 18 C-Atomen. Derartige Fettsäuren können auch in nicht vollständig neutralisierter Form eingesetzt werden. Zu den brauchbaren Tensiden des Sulfat-Typs gehören die Salze der Schwefelsäurehalbester von Fettalkoholen mit 12 bis 18 C-Atomen und die Sulfatierungsprodukte der genannten nichtionischen Tenside mit niedrigem Ethoxylierungsgrad. Zu den verwendbaren Tensiden vom Sulfonat-Typ gehören lineare Alkylbenzolsulfonate mit 9 bis 14 C-Atomen im Alkylteil, Alkansulfonate mit 12 bis 18 C-Atomen, sowie Olefinsulfonate mit 12 bis 18 C-Atomen, die bei der Umsetzung entsprechender Monoolefine mit Schwefeltrioxid entstehen, sowie alpha-Sulfofettsäureester, die bei der Sulfonierung von Fettsäuremethyl- oder -ethylestern entstehen.The compositions of the invention may contain surfactants, with preference being given to anionic surfactants, nonionic surfactants and mixtures thereof, as well as cationic surfactants. Suitable nonionic surfactants are, in particular, ethoxylation and / or propoxylation products of alkyl glycosides and / or linear or branched alcohols having in each case 12 to 18 C atoms in the alkyl moiety and 3 to 20, preferably 4 to 10, alkyl ether groups. In addition, suitable ethoxylation and / or propoxylation products of N-alkylamines, vicinal diols, fatty acid esters and fatty acid amides which correspond to said long-chain alcohol derivatives with respect to the alkyl moiety and of alkylphenols having 5 to 12 carbon atoms in the alkyl radical are useful. Suitable anionic surfactants are in particular soaps and those which contain sulfate or sulfonate groups with preferably alkali ions as cations. Usable soaps are preferably the alkali salts of the saturated or unsaturated fatty acids having 12 to 18 carbon atoms. Such fatty acids can also be used in incompletely neutralized form. Useful surfactants of the sulfate type include the salts of the sulfuric acid half-esters of fatty alcohols having 12 to 18 carbon atoms and the sulfation products of said nonionic surfactants having a low degree of ethoxylation. Suitable surfactants of the sulfonate type include linear alkylbenzenesulfonates having 9 to 14 carbon atoms in the alkyl moiety, alkanesulfonates having 12 to 18 carbon atoms, and olefin sulfonates having 12 to 18 carbon atoms, which are formed in the reaction of corresponding monoolefins with sulfur trioxide, and alpha-sulfofatty acid esters resulting from the sulfonation of fatty acid methyl or ethyl esters.

Kationische Tenside werden vorzugsweise unter den Esterquats und/oder den quaternären Ammoniumverbindungen (QAV) gemäß der allgemeinen Formel (R')(R")(R"')(RIV)N+ X~ ausgewählt, in der R1 bis Rιv für gleiche oder verschiedene C-|.22-Alkylreste, C7.28-Arylalkylreste oder heterozyklische Reste stehen, wobei zwei oder im Falle einer aromatischen Einbindung wie im Pyridin sogar drei Reste gemeinsam mit dem Stickstoffatom den Heterozyklus, z.B. eine Pyridinium- oder Imidazoliniumverbindung, bilden, und X" für Halogenidionen, Sulfationen, Hydroxidionen oder ähnliche Anionen steht. QAV sind durch Umsetzung tertiärer Amine mit Alkylierungsmitteln, wie z.B. Methylchlorid, Benzylchlorid, Dimethylsulfat, Dodecylbromid, aber auch Ethylenoxid herstellbar. Die Alkylierung von tertiären Aminen mit einem langen Alkyl-Rest und zwei Methyl-Gruppen gelingt besonders leicht, auch die Quaternierung von tertiären Aminen mit zwei langen Resten und einer Methyl-Gruppe kann mit Hilfe von Methylchlorid unter milden Bedingungen durchgeführt werden. Amine, die über drei lange Alkyl-Reste oder Hydroxy- substituierte Alkyl-Reste verfügen, sind wenig reaktiv und werden z.B. mit Dimethylsulfat quaterniert. In Frage kommende QAV sind beispielweise Benzalkoniumchlorid (N Alkyl-N,N dimethyl-benzylammoniumchlorid), Benzalkon B (m,p-Dichlorbenzyldimethyl-C12-alkylammo- niumchlorid, Benzoxoniumchlorid (Benzyl-dodecyl-bis-(2-hydroxyethyl)-ammoniumchlorid), Cetrimoniumbromid (N-Hexadecyl-N,N-trimethyl-ammoniumbromid), Benzetoniumchlorid (N, N Dimethyl-N [2-[2-[p-(1 ,1 ,3,3-tetramethylbutyl)phenoxy]-ethoxy]-ethyl]-benzylammoniumchlorid), Dialkyldimethylammoniumchloride wie Di-n-decyl-dimethyl-ammoniumchlorid, Didecyldimethylammonium-bromid, Dioctyl-dimethyl-ammoniumchlorid, 1-Cetylpyridiniumchlorid und Thiazolinjodid sowie deren Mischungen. Bevorzugte QAV sind die Benzalkoniumchloride mit C8-C22-Alkylresten, insbesondere Ci-CM-Alkyl-benzyl-dimethylammoniumchlorid.Cationic surfactants are preferably selected from esterquats and / or quaternary ammonium compounds (QAV) according to the general formula (R ') (R ") (R"') (R IV ) N + X - , in which R 1 to R iv for the same or different C |. 22- alkyl radicals, C 7 . 28 -Arylalkylreste or heterocyclic radicals, wherein two or in the case of an aromatic inclusion as in pyridine even three radicals together with the nitrogen atom, the heterocycle, such as a pyridinium or Imidazoliniumverbindung, form, and X " for halide ions, sulfate ions, hydroxide ions or similar anions QACs can be prepared by reaction of tertiary amines with alkylating agents, such as, for example, methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also ethylene oxide.The alkylation of tertiary amines with a long alkyl radical and two methyl groups is particularly easy, also the quaternization of tertiary amines having two long radicals and one methyl group can be carried out under mild conditions with the aid of methyl chloride. Amines having three long alkyl radicals or hydroxy-substituted alkyl radicals are less reactive and are quaternized, for example, with dimethyl sulfate. Eligible QACs include benzalkone ium chloride (N alkyl-N, N dimethylbenzylammonium chloride), benzalkone B (m, p-dichlorobenzyldimethyl-C 12 -alkylammonium chloride, benzoxonium chloride (benzyldodecyl-bis- (2-hydroxyethyl) -ammonium chloride), cetrimonium bromide (N- Hexadecyl-N, N-trimethyl-ammonium bromide), benzetonium chloride (N, N-dimethyl-N [2- [2- [p- (1,1,3,3-tetramethyl-butyl) -phenoxy] -ethoxy] -ethyl] -benzylammonium chloride) , Dialkyldimethylammoniumchloride such as di-n-decyl-dimethyl-ammonium chloride, Didecyldimethylammonium bromide, dioctyl-dimethyl-ammonium chloride, 1-Cetylpyridiniumchlorid and Thiazolinjodid and mixtures thereof. Preferred QUATS are the benzalkonium chlorides containing C 8 -C 22 alkyl, in particular Ci Σ -C M-alkyl-benzyl-dimethylammonium chloride.

Unter Esterquats sollen hier vorzugsweise Verbindungen der allgemeinen Formel IV, RS(CO)- C— (CH2)s X" (|γ)

Figure imgf000011_0001
Esterquats are here preferably compounds of the general formula IV, RS (CO) -C (CH 2 ) s X " (| γ)
Figure imgf000011_0001

verstanden werden, in der R5 für einen Alkyl- oder Alkenylrest mit 12 bis 22 Kohlenstoffatomen und 0, 1 , 2 oder 3 Doppelbindungen, R6 und R7 unabhängig voneinander für H, OH oder 0(CO)R5, s, t und u jeweils unabhängig voneinander für den Wert 1 , 2 oder 3 und X" für ein Anion, insbesondere Halogenid, Methosulfat, Methophosphat oder Phosphat sowie Mischungen aus diesen, steht. Bevorzugt sind Verbindungen, die für R6 die Gruppe 0(CO)R5 und für R5 einen Alkylrest mit 16 bis 18 Kohlenstoffatomen enthalten. Besonders bevorzugt sind Verbindungen, bei denen R7 zudem für OH steht. Beispiele für Verbindungen der Formel (IV) sind Methyl-N-(2-hydroxyethyl)-N,N-di(talg- acyl-oxyethyl)ammonium-methosulfat, Bis-(palmitoyl)-ethyl-hydroxyethyl-methyl-ammonium- methosulfat oder Methyl-N,N-bis(acyloxyethyl)-N-(2-hydroxyethyl)ammonium-methosulfat. Werden quarternierte Verbindungen der Formel (IV) eingesetzt, die ungesättigte Gruppen aufweisen, sind die Acylgruppen bevorzugt, deren korrespondierende Fettsäuren eine Jodzahl zwischen 5 und 80, vorzugsweise zwischen 10 und 60 und insbesondere zwischen 15 und 45 aufweisen und/oder die ein cis/trans-lsomerenverhältnis (in Mol-%) von größer als 30 : 70, vorzugsweise größer als 50 : 50 und insbesondere größer als 70 : 30 haben. Handelsübliche Beispiele sind die von der Firma Stepan unter dem Warenzeichen Stepantex® vertriebenen Methylhydroxyalkyldialkoyloxy- alkylammoniummethosulfate oder die unter dem Handelsnamen Dehyquart® bekannten Produkte der Firma Cognis Deutschland GmbH beziehungsweise die unter der Bezeichnung Rewoquat® bekannten Produkte des Herstellers Goldschmidt-Witco.in which R 5 is an alkyl or alkenyl radical having 12 to 22 carbon atoms and 0, 1, 2 or 3 double bonds, R 6 and R 7 are independently H, OH or O (CO) R 5 , s, t and u are each independently of the other the value 1, 2 or 3 and X "is an anion, in particular halide, methosulphate, methophosphate or phosphate and mixtures thereof, Preference is given to compounds which for R 6 are the group O (CO) R 5 and for R 5 contain an alkyl radical having 16 to 18 carbon atoms, particular preference is given to compounds in which R 7 additionally represents OH. Examples of compounds of the formula (IV) are methyl N- (2-hydroxyethyl) -N, N di (tallow acyl oxyethyl) ammonium methosulfate, bis (palmitoyl) ethyl hydroxyethyl methyl ammonium methosulfate or methyl N, N-bis (acyloxyethyl) -N- (2-hydroxyethyl) ammonium methosulfate If quaternized compounds of the formula (IV) which have unsaturated groups are used, the acyl groups whose k corresponding fatty acids have an iodine value between 5 and 80, preferably between 10 and 60 and in particular between 15 and 45 and / or which has a cis / trans isomer ratio (in mol%) of greater than 30:70, preferably greater than 50:50 and in particular greater than 70:30. Commercial examples are the alkylammoniummethosulfate marketed by Stepan under the trade name Stepantex® ® methyl hydroxyalkyl or known under the trade name Dehyquart® ® products from Cognis Germany GmbH or the known under the name Rewoquat ® products by manufacturer Goldschmidt-Witco.

Tenside sind in den erfindungsgemäßen Mitteln in Mengenanteilen von vorzugsweise 5 Gew.-% bis 50 Gew.-%, insbesondere von 8 Gew.-% bis 30 Gew.-%, enthalten. Insbesondere in Wäschenachbehandlungsmitteln werden vorzugsweise bis zu 30 Gew.-%, insbesondere 5 Gew.-% bis 15 Gew.-% Tenside, unter diesen bevorzugt wenigstens anteilsweise Kationtenside, eingesetzt.Surfactants are present in the inventive compositions in proportions of preferably 5 wt .-% to 50 wt .-%, in particular from 8 wt .-% to 30 wt .-%. Particularly in laundering agents, preferably up to 30% by weight, in particular from 5% by weight to 15% by weight, of surfactants, among these preferably at least partially cationic surfactants, are used.

Ein erfindungsgemäßes Mittel enthält vorzugsweise mindestens einen wasserlöslichen und/oder wasserunlöslichen, organischen und/oder anorganischen Builder. Zu den wasserlöslichen organischen Buildersubstanzen gehören Polycarbonsäuren, insbesondere Citronensäure und Zuckersäuren, monomere und polymere Aminopolycarbonsäuren, insbesondere Methylglycin- diessigsäure, Nitrilotriessigsäure und Ethylendiamintetraessigsäure sowie Polyasparaginsäure, Polyphosphonsäuren, insbesondere Aminotris(methylenphosphonsäure), Ethylendiamintetra- kis(methylenphosphonsäure) und 1-Hydroxyethan-1 ,1-diphosphonsäure, polymere Hydroxy- verbindungen wie Dextrin sowie polymere (Poly-)carbonsäuren, polymere Acrylsäuren, Methacryl- säuren, Maleinsäuren und Mischpolymere aus diesen, die auch geringe Anteile polymerisierbarer Substanzen ohne Carbonsäurefunktionalität einpolymerisiert enthalten können. Die relative Molekülmasse der Homopolymeren ungesättiger Carbonsäuren liegt im allgemeinen zwischen 5 000 und 200 000, die der Copolymeren zwischen 2 000 und 200 000, vorzugsweise 50 000 bis 120 000, jeweils bezogen auf freie Säure. Ein besonders bevorzugtes Acrylsäure-Maleinsäure- Copolymer weist eine relative Molekülmasse von 50 000 bis 100 000 auf. Geeignete, wenn auch weniger bevorzugte Verbindungen dieser Klasse sind Copolymere der Acrylsäure oder Methacryl- säure mit Vinylethern, wie Vinylmethylethern, Vinylester, Ethylen, Propylen und Styrol, in denen der Anteil der Säure mindestens 50 Gew.-% beträgt. Als wasserlösliche organische Buildersubstanzen können auch Terpolymere eingesetzt werden, die als Monomere zwei ungesättigte Säuren und/oder deren Salze sowie als drittes Monomer Vinylalkohol und/ oder ein Vinylalkohol-Derivat oder ein Kohlenhydrat enthalten. Das erste saure Monomer beziehungsweise dessen Salz leitet sich von einer monoethylenisch ungesättigten C3-C8-Carbonsäure und vorzugsweise von einer C3- C4-Monocarbonsäure, insbesondere von (Meth)-acrylsäure ab. Das zweite saure Monomer beziehungsweise dessen Salz kann ein Derivat einer C4-C8-Dicarbonsäure sein, wobei Maleinsäure besonders bevorzugt ist. Die dritte monomere Einheit wird in diesem Fall von Vinylalkohol und/oder vorzugsweise einem veresterten Vinylalkohol gebildet. Insbesondere sind Vinylalkohol-Derivate bevorzugt, welche einen Ester aus kurzkettigen Carbonsäuren, beispielsweise von d-C4-Carbonsäu- ren, mit Vinylalkohol darstellen. Bevorzugte Polymere enthalten dabei 60 Gew.-% bis 95 Gew.-%, insbesondere 70 Gew.-% bis 90 Gew.-% (Meth)acrylsäure bzw. (Meth)acrylat, besonders bevorzugt Acrylsäure bzw. Acrylat, und Maleinsäure bzw. Maleinat sowie 5 Gew.-% bis 40 Gew.- %, vorzugsweise 10 Gew.-% bis 30 Gew.-% Vinylalkohol und/oder Vinylacetat. Ganz besonders bevorzugt sind dabei Polymere, in denen das Gewichtsverhältnis von (Meth)acrylsäure beziehungsweise (Meth)acrylat zu Maleinsäure beziehungsweise Maleinat zwischen 1 :1 und 4:1 , vorzugsweise zwischen 2:1 und 3:1 und insbesondere 2:1 und 2,5:1 liegt. Dabei sind sowohl die Mengen als auch die Gewichtsverhältnisse auf die Säuren bezogen. Das zweite saure Monomer beziehungsweise dessen Salz kann auch ein Derivat einer Allylsulfonsäure sein, die in 2-Stellung mit einem Alkylrest, vorzugsweise mit einem d-C4-Alkylrest, oder einem aromatischen Rest, der sich vorzugsweise von Benzol oder Benzol-Derivaten ableitet, substituiert ist. Bevorzugte Terpolymere enthalten dabei 40 Gew.-% bis 60 Gew.-%, insbesondere 45 bis 55 Gew.-% (Meth)acrylsäure beziehungsweise (Meth)acrylat, besonders bevorzugt Acrylsäure beziehungsweise Acrylat, 10 Gew.-% bis 30 Gew.-%, vorzugsweise 15 Gew.-% bis 25 Gew.-% Methallylsulfonsäure bzw. Methallylsulfonat und als drittes Monomer 15 Gew.-% bis 40 Gew.-%, vorzugsweise 20 Gew.-% bis 40 Gew.-% eines Kohlenhydrats. Dieses Kohlenhydrat kann dabei beispielsweise ein Mono-, Di-, Oligo- oder Polysaccharid sein, wobei Mono-, Di- oder Oligosaccharide bevorzugt sind. Besonders bevorzugt ist Saccharose. Durch den Einsatz des dritten Monomers werden vermutlich Sollbruchstellen in das Polymer eingebaut, die für die gute biologische Abbaubarkeit des Polymers verantwortlich sind. Diese Terpolymere weisen im Allgemeinen eine relative Molekülmasse zwischen 1 000 und 200 000, vorzugsweise zwischen 200 und 50 000 und insbesondere zwischen 3 000 und 10 000 auf. Weitere bevorzugte Copolymere sind solche, die als Monomere Acrolein und Acrylsäure/Acrylsäuresalze bzw. Vinylacetat aufweisen. Die organischen Buildersubstanzen können, insbesondere zur Herstellung flüssiger Mittel, in Form wäßriger Lösungen, vorzugsweise in Form 30- bis 50-gewichtsprozentiger wäßriger Lösungen eingesetzt werden. Alle genannten Säuren werden in der Regel in Form ihrer wasserlöslichen Salze, insbesondere ihre Alkalisalze, eingesetzt.An agent according to the invention preferably contains at least one water-soluble and / or water-insoluble, organic and / or inorganic builder. The water-soluble organic builder substances include polycarboxylic acids, in particular citric acid and sugar acids, monomeric and polymeric aminopolycarboxylic acids, in particular methylglycine diacetic acid, nitrilotriacetic acid and ethylenediaminetetraacetic acid and polyaspartic acid, polyphosphonic acids, in particular aminotris (methylenephosphonic acid), ethylenediaminetetrakis (methylenephosphonic acid) and 1-hydroxyethane-1, 1-diphosphonic acid, polymeric hydroxy compounds such as dextrin and also polymeric (poly) carboxylic acids, polymeric acrylic acids, methacrylic acids, maleic acids and mixed polymers thereof, which also polymerize small amounts May contain copolymerized substances without carboxylic acid functionality. The molecular weight of the homopolymers of unsaturated carboxylic acids is generally between 5,000 and 200,000, that of the copolymers between 2,000 and 200,000, preferably 50,000 to 120,000, in each case based on the free acid. A particularly preferred acrylic acid-maleic acid copolymer has a molecular weight of 50,000 to 100,000. Suitable, albeit less preferred, compounds of this class are copolymers of acrylic acid or methacrylic acid with vinyl ethers, such as vinylmethyl ethers, vinyl esters, ethylene, propylene and styrene, in which the proportion of the acid is at least 50% by weight. As water-soluble organic builders, it is also possible to use terpolymers which contain two unsaturated acids and / or salts thereof as monomers and vinyl alcohol and / or a vinyl alcohol derivative or a carbohydrate as the third monomer. The first acidic monomer or its salt is derived from a monoethylenically unsaturated C 3 -C 8 -carboxylic acid and preferably from a C 3 - C 4 -monocarboxylic acid, in particular from (meth) -acrylic acid. The second acidic monomer or its salt can be a derivative of a C 4 -C 8 -dicarboxylic acid, with maleic acid being particularly preferred. The third monomeric unit is formed in this case of vinyl alcohol and / or preferably an esterified vinyl alcohol. In particular, vinyl alcohol derivatives are preferred which represent an ester of short-chain carboxylic acids, for example of C 1 -C 4 -carboxylic acids, with vinyl alcohol. Preferred polymers contain from 60% by weight to 95% by weight, in particular from 70% by weight to 90% by weight, of (meth) acrylic acid or (meth) acrylate, particularly preferably acrylic acid or acrylate, and maleic acid or Maleinate and 5 wt .-% to 40% by weight, preferably 10 wt .-% to 30 wt .-% of vinyl alcohol and / or vinyl acetate. Very particular preference is given to polymers in which the weight ratio of (meth) acrylic acid or (meth) acrylate to maleic acid or maleate is between 1: 1 and 4: 1, preferably between 2: 1 and 3: 1 and in particular 2: 1 and 2 , 5: 1 lies. Both the amounts and the weight ratios are based on the acids. The second acidic monomer or its salt can also be a derivative of an allylsulfonic acid which is substituted in the 2-position by an alkyl radical, preferably by a C 1 -C 4 -alkyl radical, or by an aromatic radical which is preferably derived from benzene or benzene derivatives , Preferred terpolymers contain from 40% by weight to 60% by weight, in particular from 45 to 55% by weight, of (meth) acrylic acid or (meth) acrylate, particularly preferably acrylic acid or acrylate, from 10% by weight to 30% by weight. %, preferably 15 wt .-% to 25 wt .-% methallylsulfonic acid or Methallylsulfonat and as the third monomer 15 wt .-% to 40 wt .-%, preferably 20 wt .-% to 40 wt .-% of a carbohydrate. This carbohydrate may be, for example, a mono-, di-, oligo- or polysaccharide, mono-, di- or oligosaccharides being preferred. Particularly preferred is sucrose. The use of the third monomer presumably incorporates predetermined breaking points into the polymer which are responsible for the good biodegradability of the polymer. These terpolymers generally have a molecular weight between 1,000 and 200,000, preferably between 200 and 50,000 and especially between 3 000 and 10 000 on. Further preferred copolymers are those which contain acrolein and acrylic acid / acrylic acid salts or vinyl acetate as monomers. The organic builder substances can be used, in particular for the preparation of liquid agents, in the form of aqueous solutions, preferably in the form of 30 to 50 percent by weight aqueous solutions. All of the acids mentioned are generally used in the form of their water-soluble salts, in particular their alkali metal salts.

Organische Buildersubstanzen können gewünschtenfalls in Mengen bis zu 40 Gew.-%, insbesondere bis zu 25 Gew.-% und vorzugsweise von 1 Gew.-% bis 8 Gew.-% enthalten sein. Mengen nahe der genannten Obergrenze werden vorzugsweise in pastenförmigen oder flüssigen, insbesondere wasserhaltigen, erfindungsgemäßen Mitteln eingesetzt. Erfindungsgemäße Wäschenachbehandlungsmittel, wie z.B. Weichspüler, können gegebenenfalls auch frei von organischem Builder sein.If desired, organic builder substances may be present in amounts of up to 40% by weight, in particular up to 25% by weight and preferably from 1% by weight to 8% by weight. Quantities close to the stated upper limit are preferably used in paste-form or liquid, in particular water-containing, agents according to the invention. Aftertreatment agents according to the invention, such as e.g. Softener, may optionally also be free of organic builder.

Als wasserlösliche anorganische Buildermaterialien kommen insbesondere Alkalisilikate und PoIy- phosphate, vorzugsweise Natriumtriphosphat, in Betracht. Als wasserunlösliche, wasserdispergier- bare anorganische Buildermaterialien können insbesondere kristalline oder amorphe Alkalialunnosilikate, gewünschtenfalls in Mengen von bis zu 50 Gew.-%, vorzugsweise nicht über 40 Gew.-% und in flüssigen Mitteln insbesondere von 1 Gew.-% bis 5 Gew.-%, eingesetzt werden. Unter diesen sind die kristallinen Natriumalumosilikate in Waschmittelqualität, insbesondere Zeolith A, P und gegebenenfalls X, bevorzugt. Mengen nahe der genannten Obergrenze werden vorzugsweise in festen, teilchenförmigen Mitteln eingesetzt. Geeignete Alumosilikate weisen insbesondere keine Teilchen mit einer Korngröße über 30 μm auf und bestehen vorzugsweise zu wenigstens 80 Gew.-% aus Teilchen mit einer Größe unter 10 μm.Suitable water-soluble inorganic builder materials are, in particular, alkali metal silicates and polyphosphates, preferably sodium triphosphate. Crystalline or amorphous alkali metal nanosilicates, if desired in amounts of up to 50% by weight, preferably not more than 40% by weight and in liquid media, in particular from 1% by weight to 5% by weight, can be used as water-insoluble, water-dispersible inorganic builder materials. -%, are used. Among these, preferred are the detergent grade crystalline sodium aluminosilicates, especially zeolite A, P and optionally X. Amounts near the above upper limit are preferably used in solid, particulate agents. In particular, suitable aluminosilicates have no particles with a particle size greater than 30 .mu.m and preferably consist of at least 80% by weight of particles having a size of less than 10 .mu.m.

Geeignete Substitute beziehungsweise Teilsubstitute für das genannte Alumosilikat sind kristalline Alkalisilikate, die allein oder im Gemisch mit amorphen Silikaten vorliegen können. Die in den erfindungsgemäßen Mitteln als Gerüststoffe brauchbaren Alkalisilikate weisen vorzugsweise ein molares Verhältnis von Alkalioxid zu SiO2 unter 0,95, insbesondere von 1 :1 ,1 bis 1 :12 auf und können amorph oder kristallin vorliegen. Bevorzugte Alkalisilikate sind die Natriumsilikate, insbesondere die amorphen Natriumsilikate, mit einem molaren Verhältnis Na2O:SiO2 von 1 :2 bis 1 :2,8. Als kristalline Silikate, die allein oder im Gemisch mit amorphen Silikaten vorliegen können, werden vorzugsweise kristalline Schichtsilikate der allgemeinen Formel Na2SixO2x+1 y H2O eingesetzt, in der x, das sogenannte Modul, eine Zahl von 1 ,9 bis 4 und y eine Zahl von 0 bis 20 ist und bevorzugte Werte für x 2, 3 oder 4 sind. Bevorzugte kristalline Schichtsilikate sind solche, bei denen x in der genannten allgemeinen Formel die Werte 2 oder 3 annimmt. Insbesondere sind sowohl ß- als auch δ-Natriumdisilikate (Na2Si2O5 y H2O) bevorzugt. Auch aus amorphen Alkalisilikaten hergestellte, praktisch wasserfreie kristalline Alkalisilikate der obengenannten allgemeinen Formel, in der x eine Zahl von 1 ,9 bis 2,1 bedeutet, können in erfindungsgemäßen Mitteln eingesetzt werden. In einer weiteren bevorzugten Ausführungsform erfindungsgemäßer Mittel wird ein kristallines Natriumschichtsilikat mit einem Modul von 2 bis 3 eingesetzt, wie es aus Sand und Soda hergestellt werden kann. Kristalline Natriumsilikate mit einem Modul im Bereich von 1 ,9 bis 3,5 werden in einer weiteren bevorzugten Ausführungsform erfindungsgemäßer Mittel eingesetzt. Falls als zusätzliche Buildersubstanz auch Alkalialumosilikat, insbesondere Zeolith, vorhanden ist, beträgt das Gewichtsverhältnis Alumosilikat zu Silikat, jeweils bezogen auf wasserfreie Aktivsubstanzen, vorzugsweise 1 :10 bis 10:1. In Mitteln, die sowohl amorphe als auch kristalline Alkalisilikate enthalten, beträgt das Gewichtsverhältnis von amorphem Alkalisilikat zu kristallinem Alkalisilikat vorzugsweise 1 :2 bis 2:1 und insbesondere 1 :1 bis 2:1.Suitable substitutes or partial substitutes for the said aluminosilicate are crystalline alkali silicates which may be present alone or in a mixture with amorphous silicates. The alkali metal silicates useful as builders in the compositions according to the invention preferably have a molar ratio of alkali metal oxide to SiO 2 of less than 0.95, in particular of 1: 1, 1 to 1: 12, and may be amorphous or crystalline. Preferred alkali metal silicates are the sodium silicates, in particular the amorphous sodium silicates, with a molar ratio of Na 2 O: SiO 2 of 1: 2 to 1: 2.8. The crystalline silicates which may be present alone or in admixture with amorphous silicates, are crystalline layer silicates with the general formula Na 2 Si x O y are used 2x + 1 H 2 O, in which x, known as the modulus, an integer of 1, 9 to 4 and y is a number from 0 to 20 and preferred values for x are 2, 3 or 4. Preferred crystalline phyllosilicates are those in which x in the abovementioned general formula assumes the values 2 or 3. In particular, both β- and δ-sodium disilicates (Na 2 Si 2 O 5 y H 2 O) are preferred. Also prepared from amorphous alkali silicates, practically anhydrous crystalline alkali silicates of the above general Formula in which x is a number from 1, 9 to 2.1, can be used in inventive compositions. In a further preferred embodiment of the composition according to the invention, a crystalline sodium layer silicate with a modulus of 2 to 3 is used, as can be prepared from sand and soda. Crystalline sodium silicates with a modulus in the range of 1.9 to 3.5 are used in a further preferred embodiment of compositions according to the invention. If alkali metal aluminosilicate, in particular zeolite, is also present as an additional builder substance, the weight ratio of aluminosilicate to silicate, in each case based on anhydrous active substances, is preferably 1:10 to 10: 1. In agents containing both amorphous and crystalline alkali metal silicates, the weight ratio of amorphous alkali metal silicate to crystalline alkali metal silicate is preferably 1: 2 to 2: 1 and especially 1: 1 to 2: 1.

Buildersubstanzen sind gewünschtenfalls in den erfindungsgemäßen Mitteln vorzugsweise in Mengen bis zu 60 Gew.-%, insbesondere von 5 Gew.-% bis 40 Gew.-%, enthalten. Erfindungsgemäße Wäschenachbehandlungsmittel, wie z.B. Weichspüler, sind vorzugsweise frei von anorganischem Builder.If desired, builder substances are preferably present in the compositions according to the invention in amounts of up to 60% by weight, in particular from 5% by weight to 40% by weight. Aftertreatment agents according to the invention, such as e.g. Softener, are preferably free of inorganic builder.

Als geeignete Persauerstoffverbindungen kommen insbesondere organische Persäuren beziehungsweise persaure Salze organischer Säuren, wie Phthalimidopercapronsäure, Perbenzoe- säure oder Salze der Diperdodecandisäure, Wasserstoffperoxid und unter den Anwendungsbedingungen Wasserstoffperoxid abgebende anorganische Salze, wie Perborat, Percarbonat und/oder Persilikat, in Betracht. Sofern feste Persauerstoffverbindungen eingesetzt werden sollen, können diese in Form von Pulvern oder Granulaten verwendet werden, die auch in im Prinzip bekannter Weise umhüllt sein können. Besonders bevorzugt wird Alkalipercarbonat, Alkaliperborat- Monohydrat oder insbesondere in flüssigen Mitteln Wasserstoffperoxid in Form wäßriger Lösungen, die 3 Gew.-% bis 10 Gew.-% Wasserstoffperoxid enthalten, eingesetzt. Falls ein erfindungsgemäßes Mittel Bleichmittel, wie vorzugsweise Persauerstoffverbindungen, enthält, sind diese in Mengen von vorzugsweise bis zu 50 Gew.-%, insbesondere von 5 Gew.-% bis 30 Gew.-%, vorhanden. Der Zusatz geringer Mengen bekannter Bleichmittelstabilisatoren wie beispielsweise von Phosphonaten, Boraten bzw. Metaboraten und Metasilikaten sowie Magnesiumsalzen wie Magnesiumsulfat kann zweckdienlich sein.Suitable peroxygen compounds are, in particular, organic peracids or pers acid salts of organic acids, such as phthalimidopercaproic acid, perbenzoic acid or salts of diperdodecanedioic acid, hydrogen peroxide and inorganic salts which release hydrogen peroxide under the conditions of use, such as perborate, percarbonate and / or persilicate. If solid peroxygen compounds are to be used, they can be used in the form of powders or granules, which can also be enveloped in a manner known in principle. Particular preference is given to using alkali percarbonate, alkali perborate monohydrate or, in particular, in liquid media, hydrogen peroxide in the form of aqueous solutions containing from 3% by weight to 10% by weight of hydrogen peroxide. If an agent according to the invention contains bleaches, such as preferably peroxygen compounds, they are present in amounts of preferably up to 50% by weight, in particular from 5% by weight to 30% by weight. The addition of small amounts of known bleach stabilizers such as phosphonates, borates or metaborates and metasilicates and magnesium salts such as magnesium sulfate may be useful.

Als Bleichaktivatoren können Verbindungen, die unter Perhydrolysebedingungen aliphatische Peroxocarbonsäuren mit vorzugsweise 1 bis 10 C-Atomen, insbesondere 2 bis 4 C-Atomen, und/oder gegebenenfalls substituierte Perbenzoesäure ergeben, eingesetzt werden. Geeignet sind Substanzen, die O- und/oder N-Acylgruppen der genannten C-Atomzahl und/oder gegebenenfalls substituierte Benzoylgruppen tragen. Bevorzugt sind mehrfach acylierte Alkylendiamine, insbesondere Tetraacetylethylendiamin (TAED), acylierte Triazinderivate, insbesondere 1 ,5- Diacetyl-2,4-dioxohexahydro-1 ,3,5-triazin (DADHT), acylierte Glykolurile, insbesondere Tetra- acetylglykoluril (TAGU), N-Acylimide, insbesondere N-Nonanoylsuccinimid (NOSI), acylierte Phenolsulfonate, insbesondere n-Nonanoyl- oder Isononanoyloxybenzolsulfonat (n- bzw. iso- NOBS), Carbonsäureanhydride, insbesondere Phthalsäureanhydrid, acylierte mehrwertige Alkohole, insbesondere Triacetin, Ethylenglykoldiacetat, 2,5-Diacetoxy-2,5-dihydrofuran und Enolester sowie acetyliertes Sorbitol und Mannitol beziehungsweise deren Mischungen (SORMAN), acylierte Zuckerderivate, insbesondere Pentaacetylglukose (PAG), Pentaacetylfruktose, Tetraacetylxylose und Octaacetyllactose sowie acetyliertes, gegebenenfalls N-alkyliertes Glucamin und Gluconolacton, und/oder N-acylierte Lactame, beispielsweise N-Benzoylcaprolactam. Hydrophil substituierte Acylacetale und Acyllactame werden ebenfalls bevorzugt eingesetzt. Auch Kombinationen konventioneller Bleichaktivatoren können eingesetzt werden. Derartige Bleichaktivatoren können im üblichen Mengenbereich, vorzugsweise in Mengen von 1 Gew.-% bis 10 Gew.-%, insbesondere 2 Gew.-% bis 8 Gew.-%, bezogen auf gesamtes Mittel, enthalten sein.As bleach activators, it is possible to use compounds which, under perhydrolysis conditions, give aliphatic peroxycarboxylic acids having preferably 1 to 10 C atoms, in particular 2 to 4 C atoms, and / or optionally substituted perbenzoic acid. Suitable substances are those which carry O- and / or N-acyl groups of the stated C atom number and / or optionally substituted benzoyl groups. Preference is given to polyacylated alkylenediamines, in particular tetraacetylethylenediamine (TAED), acylated triazine derivatives, in particular 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine (DADHT), acylated glycolurils, in particular tetraacetylenediamines. acetylglycoluril (TAGU), N-acylimides, in particular N-nonanoylsuccinimide (NOSI), acylated phenolsulfonates, in particular n-nonanoyl or isononanoyloxybenzenesulfonate (n- or iso-NOBS), carboxylic anhydrides, in particular phthalic anhydride, acylated polyhydric alcohols, in particular triacetin, ethylene glycol diacetate , 2,5-diacetoxy-2,5-dihydrofuran and enol esters, as well as acetylated sorbitol and mannitol or mixtures thereof (SORMAN), acylated sugar derivatives, in particular pentaacetylglucose (PAG), pentaacetyl fructose, tetraacetylxylose and octaacetyl lactose as well as acetylated, optionally N-alkylated glucamine and gluconolactone , and / or N-acylated lactams, for example N-benzoyl-caprolactam. Hydrophilic substituted acyl acetals and acyl lactams are also preferably used. Combinations of conventional bleach activators can also be used. Such bleach activators may be present in the customary amount range, preferably in amounts of from 1% by weight to 10% by weight, in particular from 2% by weight to 8% by weight, based on the total agent.

Zusätzlich zu den oben aufgeführten konventionellen Bleichaktivatoren oder an deren Stelle können auch Sulfonimine und/oder bleichverstärkende Übergangsmetallsalze beziehungsweise Übergangsmetallkomplexe als sogenannte Bleichkatalysatoren enthalten sein. Zu den in Frage kommenden Übergangsmetallverbindungen gehören insbesondere Mangan-, Eisen-, Cobalt-, Ruthenium- oder Molybdän-Salenkomplexe und deren N-Analogverbindungen, Mangan-, Eisen-, Cobalt-, Ruthenium- oder Molybdän-Carbonylkomplexe, Mangan-, Eisen-, Cobalt-, Ruthenium-, Molybdän-, Titan-, Vanadium- und Kupfer-Komplexe mit stickstoffhaltigen Tripod-Liganden, Cobalt-, Eisen-, Kupfer- und Ruthenium-Amminkomplexe. Kombinationen aus Bleichaktivatoren und Übergangsmetall-Bleichkatalysatoren können ebenfalls eingesetzt werden. Bleichverstärkende Übergangsmetallkomplexe, insbesondere mit den Zentralatomen Mn, Fe, Co, Cu, Mo, V, Ti und/oder Ru, können in üblichen Mengen, vorzugsweise in einer Menge bis zu 1 Gew.-%, insbesondere von 0,0025 Gew.-% bis 0,25 Gew.-% und besonders bevorzugt von 0,01 Gew.-% bis 0,1 Gew.-%, jeweils bezogen auf gesamtes Mittel, eingesetzt werden.In addition to the conventional bleach activators listed above or in their place, sulfone imines and / or bleach-enhancing transition metal salts or transition metal complexes can also be present as so-called bleach catalysts. Suitable transition metal compounds include, in particular, manganese, iron, cobalt, ruthenium or molybdenum-salene complexes and their N-analogues, manganese, iron, cobalt, ruthenium or molybdenum carbonyl complexes, manganese, iron, , Cobalt, ruthenium, molybdenum, titanium, vanadium, and copper complexes with nitrogen-containing tripod ligands, cobalt, iron, copper, and ruthenium-ammine complexes. Combinations of bleach activators and transition metal bleach catalysts can also be used. Bleach-enhancing transition metal complexes, in particular having the central atoms Mn, Fe, Co, Cu, Mo, V, Ti and / or Ru, can be used in customary amounts, preferably in an amount of up to 1% by weight, in particular 0.0025% by weight. % to 0.25 wt .-% and particularly preferably from 0.01 wt .-% to 0.1 wt .-%, each based on the total agent used.

Als in den Mitteln verwendbare Enzyme kommen solche aus der Klasse der Proteasen, Cutinasen, Amylasen, Pullulanasen, Hemicellulasen, Cellulasen, Lipasen, Oxidasen und Peroxidasen sowie deren Gemische in Frage. Besonders geeignet sind aus Pilzen oder Bakterien, wie Bacillus subtilis, Bacillus licheniformis, Streptomyces griseus, Humicola lanuginosa, Humicola insolens, Pseudomonas pseudoalcaligenes oder Pseudomonas cepacia gewonnene enzymatische Wirkstoffe. Die gegebenenfalls verwendeten Enzyme können an Trägerstoffen adsorbiert und/oder in Hüllsubstanzen eingebettet sein, um sie gegen vorzeitige Inaktivierung zu schützen. Sie sind gewünschtenfalls in den erfindungsgemäßen Mitteln vorzugsweise in Mengen nicht über 5 Gew.-%, insbesondere von 0,2 Gew.-% bis 2 Gew.-%, enthalten. Die Mittel können als optische Aufheller beispielsweise Derivate der Diaminostilbendisulfonsäure beziehungsweise deren Alkalimetallsalze enthalten. Geeignet sind zum Beispiel Salze der 4,4'- Bis(2-anilino-4-morpholino-1 ,3,5-triazinyl-6-annino)stilben-2,2'-disulfonsäure oder gleichartig aufgebaute Verbindungen, die anstelle der Morpholino-Gruppe eine Diethanolaminogruppe, eine Methylaminogruppe, eine Anilinogruppe oder eine 2-Methoxyethylaminogruppe tragen. Weiterhin können Aufheller vom Typ der substituierten Diphenylstyryle anwesend sein, zum Beispiel die Alkalisalze des 4,4'-Bis(2-sulfostyryl)-diphenyls, 4,4'-Bis(4-chlor-3-sulfostyryl)-diphenyls oder 4-(4- Chlorstyryl)-4'-(2-sulfostyryl)-diphenyls. Auch Gemische der vorgenannten Aufheller können verwendet werden.Suitable enzymes which can be used in the compositions are those from the class of proteases, cutinases, amylases, pullulanases, hemicellulases, cellulases, lipases, oxidases and peroxidases and mixtures thereof. Particularly suitable are from fungi or bacteria, such as Bacillus subtilis, Bacillus licheniformis, Streptomyces griseus, Humicola lanuginosa, Humicola insolens, Pseudomonas pseudoalcaligenes or Pseudomonas cepacia derived enzymatic agents. The optionally used enzymes may be adsorbed to carriers and / or embedded in encapsulants to protect against premature inactivation. If desired, they are preferably present in the compositions according to the invention in amounts of not more than 5% by weight, in particular from 0.2% by weight to 2% by weight. The agents may contain, for example, derivatives of diaminostilbenedisulfonic acid or their alkali metal salts as optical brighteners. For example, salts of 4,4'-bis (2-anilino-4-morpholino-1, 3,5-triazinyl-6-annino) stilbene-2,2'-disulphonic acid or similarly constructed compounds which replace the morpholino Group carry a diethanolamino group, a methylamino group, an anilino group or a 2-methoxyethylamino group. Furthermore, brighteners of the substituted diphenylstyrene type may be present, for example the alkali metal salts of 4,4'-bis (2-sulfostyryl) -diphenyl, 4,4'-bis (4-chloro-3-sulfostyryl) -diphenyl or 4- (4-chlorostyryl) -4 '- (2-sulfostyryl) -diphenyls. Mixtures of the aforementioned brightener can be used.

Zu den geeigneten Schauminhibitoren gehören beispielsweise Organopolysiloxane und deren Gemische mit mikrofeiner, gegebenenfalls signierter Kieselsäure sowie Pa-raffinwachse und deren Gemische mit silanierter Kieselsäure oder Bisfettsäure-alkylendiamiden. Mit Vorteilen werden auch Gemische aus verschiedenen Schaum-inhibitoren verwendet, zum Beispiel solche aus Silikonen, Paraffinen oder Wachsen. Vorzugsweise sind die Schauminhibitoren, insbesondere Silikon- und/oder Paraffin-haltige Schauminhibitoren, an eine granuläre, in Wasser lösliche beziehungsweise dispergierbare Trägersubstanz gebunden. Insbesondere sind dabei Mischungen aus Paraffinwachsen und Bistearylethylendiamiden bevorzugt.Suitable foam inhibitors include, for example, organopolysiloxanes and mixtures thereof with microfine, optionally signed silica and also Pa raffinwachse and mixtures thereof with silanated silica or bis-fatty acid alkylenediamides. It is also advantageous to use mixtures of various foam inhibitors, for example those of silicones, paraffins or waxes. Preferably, the foam inhibitors, in particular silicone and / or paraffin-containing foam inhibitors, are bound to a granular, water-soluble or dispersible carrier substance. In particular, mixtures of paraffin waxes and bistearylethylenediamides are preferred.

Zusätzlich können die Mittel auch Komponenten enthalten, welche die Öl- und Fettauswaschbarkeit aus Textilien positiv beeinflussen, sogenannte soil release-Wirkstoffe. Dieser Effekt wird besonders deutlich, wenn ein Textil verschmutzt wird, das bereits vorher mehrfach mit einem erfindungsgemäßen Mittel, das diese öl- und fettlösende Komponente enthält, gewaschen wurde. Zu den bevorzugten öl- und fettlösenden Komponenten zählen beispielsweise nichtionische Celluloseether wie Methylcellulose und Methylhydroxypropylcellulose mit einem Anteil an Methoxyl-Gruppen von 15 bis 30 Gew.-% und an Hydroxypropoxyl-Gruppen von 1 bis 15 Gew.-%, jeweils bezogen auf den nichtionischen Celluloseether, sowie die aus dem Stand der Technik bekannten Polymere der Phthalsäure und/oder der Terephthalsäure bzw. von deren Derivaten mit monomeren und/oder polymeren Diolen, insbesondere Polymere aus Ethylenterephthalaten und/oder Polyethylenglykolterephthalaten oder anionisch und/oder nichtionisch modifizierten Derivaten von diesen.In addition, the compositions may also contain components which positively influence the oil and Fettauswaschbarkeit from textiles, so-called soil release agents. This effect becomes particularly evident when a textile is soiled which has previously been washed several times with an agent according to the invention containing this oil and fat-dissolving component. The preferred oil and fat dissolving components include, for example, nonionic cellulose ethers such as methylcellulose and methylhydroxypropylcellulose with a proportion of methoxyl groups of 15 to 30 wt .-% and hydroxypropoxyl groups of 1 to 15 wt .-%, each based on the nonionic Cellulose ethers, and the known from the prior art polymers of phthalic acid and / or terephthalic acid or derivatives thereof with monomeric and / or polymeric diols, in particular polymers of ethylene terephthalates and / or polyethylene glycol terephthalates or anionic and / or nonionic modified derivatives thereof.

Die Mittel können auch Farbübertragungsinhibitoren, vorzugsweise in Mengen von 0,1 Gew.-% bis 2 Gew.-%, insbesondere 0,1 Gew.-% bis 1 Gew.-%, enthalten, die in einer bevorzugten Ausgestaltung der Erfindung Polymere aus Vinylpyrrolidon, Vinylimidazol, Vinylpyridin-N-Oxid oder Copolymere aus diesen sind. Brauchbar sind sowohl Polyvinylpyrrolidone mit Molgewichten von 15 000 bis 50 000 wie auch Polyvinylpyrrolidone mit Molgewichten über 1 000 000, insbesondere von 1 500 000 bis 4 000 000, N-Vinylimidazol/N-Vinylpyrrolidon-Copolymere, Polyvinyloxazolidone, Copolymere auf Basis von Vinylmonomeren und Carbonsäureamiden, pyrrolidongruppenhaltige Polyester und Polyamide, gepfropfte Polyamidoamine und Polyethylenimine, Polymere mit Amidgruppen aus sekundären Aminen, Polyamin-N-Oxid-Polymere, Polyvinylalkohole und Copolymere auf Basis von Acrylamidoalkenylsulfonsäuren. Eingesetzt werden können aber auch enzymatische Systeme, umfassend eine Peroxidase und Wasserstoffperoxid beziehungsweise eine in Wasser Wasserstoffperoxid-Iiefernde Substanz. Der Zusatz einer Mediatorverbindung für die Peroxidase, zum Beispiel eines Acetosyringons, eines Phenolderivats oder eines Phenotiazins oder Phenoxazins, ist in diesem Fall bevorzugt, wobei auch zusätzlich obengenannte polymere Farbübertragungsinhibitorwirkstoffe eingesetzt werden können. Polyvinylpyrrolidon weist zum Einsatz in erfindungsgemäßen Mitteln vorzugsweise eine durchschnittliche Molmasse im Bereich von 10 000 bis 60 000, insbesondere im Bereich von 25 000 bis 50 000 auf. Unter den Copolymeren sind solche aus Vinylpyrrolidon und Vinylimidazol im Molverhältnis 5:1 bis 1 :1 mit einer durchschnittlichen Molmasse im Bereich von 5 000 bis 50 000, insbesondere 10 000 bis 20 000 bevorzugt.The compositions may also color transfer inhibitors, preferably in amounts of from 0.1 wt .-% to 2 wt .-%, in particular 0.1 wt .-% to 1 wt .-%, containing in a preferred embodiment of the invention polymers Vinylpyrrolidone, vinylimidazole, vinylpyridine N-oxide or copolymers of these are. Useful are both polyvinylpyrrolidones having molecular weights of from 15,000 to 50,000 and polyvinylpyrrolidones having molecular weights of more than 1,000,000, in particular from 1,500,000 to 4,000,000, N-vinylimidazole / N-vinylpyrrolidone copolymers, polyvinyloxazolidones, Copolymers based on vinyl monomers and carboxamides, pyrrolidone group-containing polyesters and polyamides, grafted polyamidoamines and polyethyleneimines, polymers with amide groups of secondary amines, polyamine-N-oxide polymers, polyvinyl alcohols and copolymers based on acrylamidoalkenylsulfonic acids. However, it is also possible to use enzymatic systems comprising a peroxidase and hydrogen peroxide or a substance which gives off hydrogen peroxide in water. The addition of a mediator compound for the peroxidase, for example an acetosyringone, a phenol derivative or a phenotiazine or phenoxazine, is preferred in this case, whereby also above-mentioned polymeric Farbübertragungsinhibitorwirkstoffe can be used. Polyvinylpyrrolidone preferably has an average molecular weight in the range from 10 000 to 60 000, in particular in the range from 25 000 to 50 000, for use in compositions according to the invention. Among the copolymers, those of vinylpyrrolidone and vinylimidazole in a molar ratio of 5: 1 to 1: 1 having an average molecular weight in the range of 5,000 to 50,000, especially 10,000 to 20,000 are preferred.

Vergrauungsinhibitoren haben die Aufgabe, den von der Textilfaser abgelösten Schmutz in der Flotte suspendiert zu halten. Hierzu sind wasserlösliche Kolloide meist organischer Natur geeignet, beispielsweise Stärke, Leim, Gelatine, Salze von Ethercarbonsäuren oder Ethersulfonsäuren der Stärke oder der Cellulose oder Salze von sauren Schwefelsäureestern der Cellulose oder der Stärke. Auch wasserlösliche, saure Gruppen enthaltende Polyamide sind für diesen Zweck geeignet. Weiterhin lassen sich andere als die obengenannten Stärkederivate verwenden, zum Beispiel Aldehydstärken. Bevorzugt können Celluloseether, wie Carboxymethylcellulose (Na-SaIz), Methylcellulose, Hydroxyalkylcellulose und Mischether, wie Methylhydroxyethylcellulose, Methyl- hydroxypropylcellulose, Methylcarboxymethylcellulose und deren Gemische, beispielsweise in Mengen von 0,1 bis 5 Gew.-%, bezogen auf die Mittel, eingesetzt werden.Graying inhibitors have the task of keeping suspended from the textile fiber dirt suspended in the fleet. Water-soluble colloids of mostly organic nature are suitable for this purpose, for example starch, glue, gelatin, salts of ether carboxylic acids or ether sulfonic acids of starch or of cellulose or salts of acidic sulfuric acid esters of cellulose or starch. Also, water-soluble polyamides containing acidic groups are suitable for this purpose. Furthermore, other than the above-mentioned starch derivatives can be used, for example aldehyde starches. Preference is given to using cellulose ethers, such as carboxymethylcellulose (Na salt), methylcellulose, hydroxyalkylcellulose and mixed ethers, such as methylhydroxyethylcellulose, methylhydroxypropylcellulose, methylcarboxymethylcellulose and mixtures thereof, for example in amounts of from 0.1 to 5% by weight, based on the compositions become.

Zu den in den erfindungsgemäßen Mitteln, insbesondere wenn sie in flüssiger oder pastöser Form vorliegen, verwendbaren organischen Lösungsmitteln gehören Alkohole mit 1 bis 4 C-Atomen, insbesondere Methanol, Ethanol, Isopropanol und tert.-Butanol, Diole mit 2 bis 4 C-Atomen, insbesondere Ethylenglykol und Propylenglykol, sowie deren Gemische und die aus den genannten Verbindungsklassen ableitbaren Ether. Derartige wassermischbare Lösungsmittel sind in den erfindungsgemäßen Mitteln vorzugsweise in Mengen von nicht über 30 Gew.-%, insbesondere von 6 Gew.-% bis 20 Gew.-%, vorhanden.Among the organic solvents which can be used in the compositions according to the invention, especially if they are in liquid or pasty form, are alcohols having 1 to 4 C atoms, in particular methanol, ethanol, isopropanol and tert-butanol, diols having 2 to 4 C atoms , in particular ethylene glycol and propylene glycol, and mixtures thereof and the derivable from said classes of compound ethers. Such water-miscible solvents are preferably present in the compositions according to the invention in amounts of not more than 30% by weight, in particular from 6% by weight to 20% by weight.

Zur Einstellung eines gewünschten, sich durch die Mischung der übrigen Komponenten nicht von selbst ergebenden pH-Werts können die erfindungsgemäßen Mittel System- und umweltverträgliche Säuren, insbesondere Citronensäure, Essigsäure, Weinsäure, Äpfelsäure, Milchsäure, Glykolsäure, Bernsteinsäure, Glutarsäure und/oder Adipinsäure, aber auch Mineralsäuren, ins- besondere Schwefelsäure, oder Basen, insbesondere Ammonium- oder Alkalihydroxide, enthalten. Derartige pH-Regulatoren sind in den erfindungsgemäßen Mitteln vorzugsweise nicht über 20 Gew.-%, insbesondere von 1 ,2 Gew.-% bis 17 Gew.-%, enthalten.In order to establish a desired pH, which does not naturally result from the mixture of the other components, the compositions according to the invention may contain system and environmentally acceptable acids, in particular citric acid, acetic acid, tartaric acid, malic acid, lactic acid, glycolic acid, succinic acid, glutaric acid and / or adipic acid, but also mineral acids, especially particular sulfuric acid, or bases, in particular ammonium or alkali hydroxides. Such pH regulators are preferably not more than 20 wt .-%, in particular from 1, 2 wt .-% to 17 wt .-%, contained in the inventive compositions.

Die Herstellung fester erfindungsgemäßer Mittel bereitet keine Schwierigkeiten und kann im Prinzip bekannter Weise, zum Beispiel durch Sprühtrocknen oder Granulation, erfolgen, wobei optionale Persauerstoffverbindung und optionaler Bleichkatalysator gegebenenfalls später zugesetzt werden. Zur Herstellung erfindungsgemäßer Mittel mit erhöhtem Schüttgewicht, insbesondere im Bereich von 650 g/l bis 950 g/l, ist ein einen Extrusionsschritt aufweisendes Verfahren bevorzugt. Die Herstellung flüssiger erfindungsgemäßer Mittel bereitet ebenfalls keine Schwierigkeiten und kann ebenfalls in bekannter Weise erfolgen.The preparation of solid compositions according to the invention presents no difficulties and can be carried out in a manner known in the art, for example by spray-drying or granulation, with optional peroxygen compound and optional bleach catalyst optionally being added later. For the preparation of compositions according to the invention having an increased bulk density, in particular in the range from 650 g / l to 950 g / l, a process comprising an extrusion step is preferred. The preparation of liquid inventive means also presents no difficulties and can also be done in a known manner.

Gemäß einer bevorzugten Ausführungsform kann die erfindungsgemäße Lehre dazu eingesetzt werden, den Parfümanteil in Wasch-, Reinigungs- und Körperpflegemitteln signifikant herabzusetzen. Dadurch ist es möglich, parfümierte Produkte auch für solche besonders empfindlichen Konsumenten anzubieten, die normal parfümierte Produkte aufgrund spezieller Unverträglichkeiten und Irritationen nur eingeschränkt oder gar nicht verwenden können. In diesem Zusammenhang sind vor allem Hautpflegeprodukte und Deodorantien, aber auch Waschmittel, wie z.B. Handwaschmittel zu nennen.According to a preferred embodiment, the teaching according to the invention can be used to significantly reduce the perfume fraction in washing, cleaning and personal care products. This makes it possible to offer perfumed products even for those particularly sensitive consumers who can not use normally perfumed products due to special intolerances and irritations, or only to a limited extent. In this context, especially skin care products and deodorants, but also detergents, such. To call hand detergent.

Ein bevorzugtes erfindungsgemäßes festes, insbesondere pulverförmiges Waschmittel kann neben den erfindungsgemäßen Bestandteilen (also (a) Duftaldehyde sowie (b) (ggf. substituierte) Ethylendiamine und/oder (ggf. substituierte) Propylendiamine) insbesondere noch Komponenten enthalten, die z.B. ausgewählt sind aus den folgenden:A preferred solid, in particular powdered, detergent according to the invention can contain, in addition to the constituents according to the invention (ie, (a) fragrant aldehydes and (b) (optionally substituted) ethylenediamines and / or (optionally substituted) propylenediamines), in particular also components which are e.g. are selected from the following:

- Aniontenside, wie vorzugsweise Alkylbenzolsulfonat, Alkylsulfat, z.B. in Mengen von vorzugsweise 5-30 Gew.-%Anionic surfactants, preferably alkylbenzenesulfonate, alkylsulfate, e.g. in amounts of preferably 5-30% by weight

- Nichtionische Tenside, wie vorzugsweise Fettalkoholpolyglycolether, Alkylpolyglucosid, Fettsäureglucamid z.B. in Mengen von vorzugsweise 0,5-15 Gew.-%Nonionic surfactants, such as preferably fatty alcohol polyglycol ethers, alkylpolyglucoside, fatty acid glucamide, e.g. in amounts of preferably 0.5-15% by weight

- Gerüststoffe, wie z.B. Zeolith, Polycarboxylat, Natriumeitrat, in Mengen von z.B. 0-70 Gew.-% , vorteilhafterweise 5-60 Gew.-%, vorzugsweise 10-55 Gew.-%, insbesondere 15-40 Gew.-%,Builders, e.g. Zeolite, polycarboxylate, sodium citrate, in amounts of e.g. 0-70% by weight, advantageously 5-60% by weight, preferably 10-55% by weight, in particular 15-40% by weight,

- Alkalien, wie z.B. Natriumcarbonat, in Mengen von z.B. 0-35 Gew.-% vorteilhafterweise 1-30 Gew.-%, vorzugsweise 2-25 Gew.-%, insbesondere 5-20 Gew.-%,Alkalis, e.g. Sodium carbonate, in amounts of e.g. 0-35 wt .-% advantageously 1-30 wt .-%, preferably 2-25 wt .-%, in particular 5-20 wt .-%,

- Bleichmittel, wie z.B. Natriumperborat, Natriumpercarbonat, in Mengen von z.B. 0-30 Gew.-% vorteilhafterweise 5-25 Gew.-%, vorzugsweise 10-20 Gew.-%,Bleaching agents, e.g. Sodium perborate, sodium percarbonate, in amounts of e.g. 0-30% by weight, advantageously 5-25% by weight, preferably 10-20% by weight,

- Korrosionsinhibitoren, z.B. Natriumsilicat, in Mengen von z.B. 0-10 Gew.-%, vorteilhafterweise 1-6 Gew.-%, vorzugsweise 2-5 Gew.-%, insbesondere 3-4 Gew.-%,- corrosion inhibitors, e.g. Sodium silicate, in amounts of e.g. 0-10% by weight, advantageously 1-6% by weight, preferably 2-5% by weight, in particular 3-4% by weight,

- Stabilisatoren, z.B. Phosphonate, vorteilhafterweise 0-1 Gew.-%, - Schauminhibitor, z.B. Seife, Siliconöle, Paraffine vorteilhafterweise 0-4 Gew.-%, vorzugsweise 0,1-3 Gew.-%, insbesondere 0,2-1 Gew.-%,Stabilizers, eg phosphonates, advantageously 0-1% by weight, Foam inhibitor, for example soap, silicone oils, paraffins, advantageously 0-4% by weight, preferably 0.1-3% by weight, in particular 0.2-1% by weight,

- Enzyme, z.B. Proteasen, Amylasen, Cellulasen, Lipasen, vorteilhafterweise 0-2 Gew.-%, vorzugsweise 0,2-1 Gew.-%, insbesondere 0,3-0,8 Gew.-%,Enzymes, e.g. Proteases, amylases, cellulases, lipases, advantageously 0-2% by weight, preferably 0.2-1% by weight, in particular 0.3-0.8% by weight,

- Vergrauungsinhibitor, z.B. Carboxymethylcellulose, vorteilhafterweise 0-1 Gew.-%,- grayness inhibitor, e.g. Carboxymethylcellulose, advantageously 0-1% by weight,

- Verfärbungsinhibitor, z.B. Polyvinylpyrrolidon-Derivate, vorzugsweise 0-2 Gew.-%,Discoloration inhibitor, e.g. Polyvinylpyrrolidone derivatives, preferably 0-2% by weight,

- Stellmittel, z.B. Natriumsulfat, vorteilhafterweise 0-20 Gew.-%,- Adjustment means, e.g. Sodium sulfate, advantageously 0-20% by weight,

- Optische Aufheller, z.B. Stilben-Derivat, Biphenyl-Derivat, vorteilhafterweise 0-0,4 Gew.-%, insbesondere 0,1-0,3 Gew.-%,Optical brighteners, e.g. Stilbene derivative, biphenyl derivative, advantageously 0-0.4% by weight, in particular 0.1-0.3% by weight,

- ggf. weitere Duftstoffe- If necessary, other fragrances

- ggf. Wasser- If necessary water

- ggf. Seife- if necessary, soap

- ggf. Bleichaktivatoren- optionally bleach activators

- ggf.Cellulosderivate- optionally cellulose derivatives

- ggf.Schmutzabweiser,- if necessary, dirt repellent,

Gew.-% jeweils bezogen auf das gesamte Mittel.% By weight, based in each case on the total agent.

In einer anderen bevorzugten Ausführungsform der Erfindung liegt das Wasch-, Reinigungs- oder Pflegemittel in flüssiger Form vor, vorzugsweise in Gelform. Bevorzugte flüssige Wasch-, Reinigungs- oder Pflegemittel haben Wassergehalte von z.B. 10-95 Gew.-%, vorzugsweise 20-80 Gew.-% und insbesondere 30-70 Gew.-%, bezogen auf das gesamte Mittel. Im Falle von flüssigen Konzentraten kann der Wassergehalt auch besonders gering sein, z.B. < 30 Gew.-%, vorzugsweise < 20 Gew.-%, insbesondere < 15 Gew.-% betragen, Gew.-% jeweils bezogen auf das gesamte Mittel. Die flüssigen Mittel können auch nichtwässrige Lösungsmittel enthalten.In another preferred embodiment of the invention, the washing, cleaning or care agent is in liquid form, preferably in gel form. Preferred liquid washing, cleaning or care agents have water contents of e.g. 10-95 wt .-%, preferably 20-80 wt .-% and in particular 30-70 wt .-%, based on the total agent. In the case of liquid concentrates, the water content may also be particularly low, e.g. <30 wt .-%, preferably <20 wt .-%, in particular <15 wt .-%, wt .-% in each case based on the total agent. The liquid agents may also contain non-aqueous solvents.

Ein bevorzugtes erfindungsgemäßes flüssiges, insbesondere gelförmiges Waschmittel kann neben den erfindungsgemäßen Bestandteilen insbesondere noch Komponenten enthalten, die z.B. ausgewählt sind aus den folgenden:In addition to the constituents according to the invention, a preferred liquid, in particular gel detergent according to the invention may contain, in particular, components which are e.g. are selected from the following:

- Aniontenside, wie vorzugsweise Alkylbenzolsulfonat, Alkylsulfat, z.B. in Mengen von vorzugsweise 5-40 Gew.-%Anionic surfactants, preferably alkylbenzenesulfonate, alkylsulfate, e.g. in amounts of preferably 5-40% by weight

- Nichtionische Tenside, wie vorzugsweise Fettalkoholpolyglycolether, Alkylpolyglucosid, Fettsäureglucamid z.B. in Mengen von vorzugsweise 0,5-25 Gew.-%Nonionic surfactants, such as preferably fatty alcohol polyglycol ethers, alkylpolyglucoside, fatty acid glucamide, e.g. in amounts of preferably 0.5-25% by weight

- Gerüststoffe, wie z.B. Zeolith, Polycarboxylat, Natriumeitrat, vorteilhafterweise 0-15 Gew.-%, vorzugsweise 0,01-10 Gew.-%, insbesondere 0,1-5 Gew.-%,Builders, e.g. Zeolite, polycarboxylate, sodium citrate, advantageously 0-15% by weight, preferably 0.01-10% by weight, in particular 0.1-5% by weight,

- Schauminhibitor, z.B. Seife, Siliconöle, Paraffine, in Mengen von z.B. 0-10 Gew.-%, vorteilhafterweise 0,1-4 Gew.-%, vorzugsweise 0,2-2 Gew.-%, insbesondere 1-3 Gew.-%,Foam inhibitor, e.g. Soap, silicone oils, paraffins, in amounts of e.g. 0-10 wt .-%, advantageously 0.1-4 wt .-%, preferably 0.2-2 wt .-%, in particular 1-3 wt .-%,

- Enzyme, z.B. Proteasen, Amylasen, Cellulasen, Lipasen, in Mengen von z.B. 0-3 Gew.-%, vorteilhafterweise 0,1-2 Gew.-%, vorzugsweise 0,2-1 Gew.-%, insbesondere 0,3-0,8 Gew.-%, - Optische Aufheller, z.B. Stilben-Derivat, Biphenyl-Derivat, in Mengen von z.B. 0-1 Gew.-%, vorteilhafterweise 0,1-0,3 Gew.-%, insbesondere 0,1-0,4 Gew.-%,- Enzymes, for example proteases, amylases, cellulases, lipases, in amounts of, for example, 0-3 wt .-%, advantageously 0.1-2 wt .-%, preferably 0.2-1 wt .-%, in particular 0.3 -0.8% by weight, Optical brightener, eg stilbene derivative, biphenyl derivative, in amounts of eg 0-1% by weight, advantageously 0.1-0.3% by weight, in particular 0.1-0.4% by weight .

- ggf. weitere Duftstoffe- If necessary, other fragrances

- ggf. Stabilisatoren,- stabilizers if necessary,

- Wasser- Water

- ggf. Seife, in Mengen von z.B. 0-25 Gew.-%, vorteilhafterweise 1-20 Gew.-%, vorzugsweise 2- 15 Gew.-%, insbesondere 5-10 Gew.-%,optionally soap, in quantities of e.g. 0-25% by weight, advantageously 1-20% by weight, preferably 2-15% by weight, in particular 5-10% by weight,

- ggf. Lösungsmittel (vorzugsweise Alkohole), vorteilhafterweise 0-25 Gew.-%, vorzugsweise 1-20 Gew.-%, insbesondere 2-15 Gew.-%, Gew.-% jeweils bezogen auf das gesamte Mittel.- If necessary, solvents (preferably alcohols), advantageously 0-25 wt .-%, preferably 1-20 wt .-%, in particular 2-15 wt .-%, wt .-% in each case based on the total agent.

Ein bevorzugter erfindungsgemäßer flüssiger Weichspüler kann neben den erfindungsgemäßen Bestandteilen insbesondere noch Komponenten enthalten, die ausgewählt sind aus den folgenden:In addition to the constituents according to the invention, a preferred liquid softener according to the invention may in particular also contain components which are selected from the following:

Kationische Tenside, wie insbesondere Esterquats, z.B. in Mengen von 5-30 Gew.-%,Cationic surfactants, such as in particular esterquats, e.g. in amounts of 5-30% by weight,

Cotenside, wie z.B. Glycerolmonostearat, Stearinsäure, Fettalkohole, Fettalkoholethoxylate, z.B. in Mengen von 0-5 Gew.-%, vorzugsweise 0,1-4 Gew.-%,Cosurfactants, e.g. Glycerol monostearate, stearic acid, fatty alcohols, fatty alcohol ethoxylates, e.g. in amounts of 0-5% by weight, preferably 0.1-4% by weight,

Emulgatoren, wie z.B. Fettaminethoxylate, z.B. in Mengen von 0-4 Gew.-%, vorzugsweiseEmulsifiers, e.g. Fatty amine ethoxylates, e.g. in amounts of 0-4 wt .-%, preferably

0,1-3 Gew.-%, ggf. weitere Duftstoffe0.1-3 wt .-%, optionally other perfumes

Farbstoffe, vorzugsweise im ppm-BereichDyes, preferably in the ppm range

Stabilisatoren, vorzugsweise im ppm-BereichStabilizers, preferably in the ppm range

Lösemittel, wie insbesondere Wasser, in Mengen von vorzugsweise 60-90 Gew.-%,Solvents, in particular water, in amounts of preferably 60-90% by weight,

- Gew.-% jeweils bezogen auf das gesamte Mittel. -% by weight, based in each case on the total agent.

Beispiel:Example:

Es wurde die Duftwirkung eines handelsüblichen teilchenförmigen Waschmittels untersucht, welches 0,9 Gew.-% Octanal enthielt. Dies entspricht dem Waschmittel A.The odor effect of a commercially available particulate detergent containing 0.9% by weight of octanal was investigated. This corresponds to the detergent A.

Ebenfalls wurde die Duftwirkung eines ansonsten vergleichbaren handelsüblichen teilchenförmigen Waschmittels untersucht, welches ebenfalls 0,9 Gew.-% Octanal enthielt sowie außerdem noch 1 ,4 Gew.-% N,N'-Dimethylethylendiamin. Dies entspricht dem Waschmittel B.The scent effect of an otherwise comparable commercial particulate detergent composition was also examined, which wt .-% octanal also contained 0.9, and still further 1, 4 wt .-% N, N 'dimethylethylenediamine. This corresponds to the detergent B.

Zur Untersuchung der Duftwirkung der Waschmittel A und B wurden Waschversuche in einer handelsüblichen Waschmaschine (Miele Waschautomat Typ W 1734 WPS; Waschgut: Baumwolltextilien und Halbleinen in Menge von 3,0kg; Hau ptwaschprog ramm bei 4O0C) durchgeführt.To investigate the fragrance effect of the detergent A and B washing experiments were conducted in a commercial washing machine (Miele washing machine type W 1734 WPS; washload: cotton textiles and Halbleinen in amount of 3.0 Kg; Hau ptwaschprog ramm at 4O 0 C.).

Die gewaschene Wäsche wurde anschließend einem Panel von 7 geruchlich geschulten Menschen vorgelegt, welche die Intensität des Wäscheduftes im feuchten Zustand sowie im trockenen Zustand (7 Tage nach der Wäsche) bewerteten. Zur Überprüfung des Wäscheduftes nach 7 Tagen wurde die feuchte Wäsche zuvor auf der Leine getrocknet und nach der Trocknung zusammengelegt und in einem offenen Regal aufbewahrt, bis 7 Tage seit der Wäsche vergangen waren.The washed laundry was then submitted to a panel of 7 people trained by the smell, who assessed the intensity of the laundry smell in the wet state as well as in the dry state (7 days after the laundry). To check the laundry smell after 7 days, the wet laundry was previously dried on a leash and, after drying, folded and stored in an open rack until 7 days had elapsed since the laundry.

Die Intensität wurde von jedem Bewerter auf einer Skala von 1 bis 6 bewertet, wobei der Wert 1 für einen nur schwach wahrnehmbaren Duft steht, während der Wert 6 für einen sehr intensiven Duft steht. Die Bewertung wurde zweimal wiederholt. Aus den gesamten Bewertungen wurde schließlich jeweils der gemittelte Wert berechnet. Es ergaben sich folgende gemittelte Werte:The intensity was rated by each evaluator on a scale of 1 to 6, where the value 1 stands for a fragrance that is only slightly perceptible, while the value 6 stands for a very intense fragrance. The evaluation was repeated twice. From the total ratings, the average value was finally calculated. The following average values were obtained:

Duftintensität der Duftintensität der feuchten Wäsche trockenen Wäsche nach 7 TagenFragrance intensity of the fragrance intensity of the wet laundry dry laundry after 7 days

Waschmittel A 5,3 1 ,5 Waschmittel B 4, 1 4,1Detergent A 5.3 1, 5 detergent B 4, 1 4.1

Das mit der Erfindung im Einklang stehende Waschmittel B führte folglich zu einer im Vergleich zu Waschmittel A deutlich verbesserten Duftintensität bei der trockenen Wäsche nach 7 Tagen.The laundry detergent B which was in accordance with the invention consequently resulted in a significantly improved fragrance intensity in the dry laundry after 7 days, compared with laundry detergent A.

Ebenso wurde die Duftwirkung eines handelsüblichen flüssigen Weichspülers untersucht, welcher 0,9 Gew.-% Octanal enthielt. Dies entspricht dem Weichspüler A. Ebenfalls wurde die Duftwirkung eines ansonsten vergleichbaren handelsüblichen flüssigen Weichspülers untersucht, welcher ebenfalls 0,9 Gew.-% Octanal enthielt. Dieser Weichspüler enthielt außerdem 1 ,4 Gew.-% N, N'- Dimethylethylendiannin. Dies entspricht dem Weichspüler B.Likewise, the fragrance effect of a commercial liquid softener was investigated, which contained 0.9 wt .-% octanal. This corresponds to the softener A. Also, the fragrance effect of an otherwise comparable commercial liquid softener was examined, which also contained 0.9 wt .-% octanal. This fabric softener also containing 1, 4 wt .-% N, N '- Dimethylethylendiannin. This corresponds to the fabric softener B.

Zur Untersuchung der Duftwirkung der Weichspüler A und B wurden Waschversuche in einer handelsüblichen Waschmaschine (Miele Waschautomat Typ W 1734 WPS; Waschgut: Baumwolltextilien und Halbleinen in Menge von 3,0kg; Hau ptwaschprog ramm bei 4O0C) durchgeführt.To investigate the fragrance effect of the softener A and B washing experiments were (Miele washing machine type W 1734 WPS; washload:; Hau ptwaschprog ramm at 4O 0 C cotton textiles and Halbleinen in amount of 3.0 Kg) in a commercial washing machine performed.

Die gewaschene Wäsche wurde anschließend wiederum einem Panel von 7 geruchlich geschulten Menschen vorgelegt, welche die Intensität des Wäscheduftes im feuchten Zustand sowie im trockenen Zustand (7 Tage nach der Wäsche) bewerteten, analog zur Untersuchung des Waschmittels, wie bereits beschrieben.The washed laundry was then in turn submitted to a panel of 7 people with an olfactory education, who assessed the intensity of the laundry odor in the wet state and in the dry state (7 days after washing), analogous to the investigation of the detergent, as already described.

Es ergaben sich folgende gemittelte Werte:The following average values were obtained:

Duftintensität der Duftintensität der feuchten Wäsche trockenen Wäsche nach 7 TagenFragrance intensity of the fragrance intensity of the wet laundry dry laundry after 7 days

Weichspüler A 5,7 1 ,7 Waschmittel B 4,3 3,9Fabric softener A 5,7 1, 7 detergent B 4,3 3,9

Der mit der Erfindung im Einklang stehende Weichspüler B führte folglich zu einer im Vergleich zu Weichspüler A deutlich verbesserten Duftintensität bei der trockenen Wäsche nach 7 Tagen. The softener B consistent with the invention consequently resulted in a significantly improved fragrance intensity in the dry laundry after 7 days compared to fabric softener A.

Claims

Patentansprüche: claims: 1. Wasch-, Reinigungs- oder Pflegemittel, enthaltend1. washing, cleaning or care products containing (a) Duftaldehyde sowie(a) fragrance aldehydes as well (b) (ggf. substituierte) Ethylendiamine und/oder (ggf. substituierte) Propylendiamine.(b) (optionally substituted) ethylenediamines and / or (optionally substituted) propylenediamines. 2. Mittel gemäß Anspruch 1 , dadurch gekennzeichnet, dass die Komponente (a) und die Komponente (b) getrennt in die Wasch-, Reinigungs- oder Pflegemittelmatrix zugegeben werden.2. Composition according to claim 1, characterized in that the component (a) and the component (b) are added separately in the washing, cleaning or care agent matrix. 3. Mittel gemäß einem der Ansprüche 1 oder 2, dadurch gekennzeichnet, dass als Komponente (b) 1 ,2-Diaminoethan, Propan-1 ,3-diamin, 1 ,2-Dianilinoethan, N,N'-Dimethylethylendiamin, N, N'- Diethylethyl-1 ,3-diamin, N, N'-Diisopropylethyl-1 ,3-diamin, N,N'-Dimethylpropan-1 ,3-diamin, N, N'- Diethylpropan-1 ,3-diamin und/oder N, N'-Diisopropylpropan-1 ,3-diamin eingesetzt wird.3. The composition according to any one of claims 1 or 2, characterized in that as component (b) 1, 2-diaminoethane, propane-1, 3-diamine, 1, 2-dianilinoethane, N, N '-dimethylethylenediamine, N, N '- diethyl ethyl-1, 3-diamine, N, N'-Diisopropylethyl-1, 3-diamine, N, N' -Dimethylpropan-1, 3-diamine, N, N'-diethylpropane-1, 3-diamine and / or N, N'-diisopropylpropane-1,3-diamine is used. 4. Mittel gemäß einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, dass als Komponente (a) ein Duftaldehyd eingesetzt wird, ausgewählt aus Adoxal, Anisaldehyd, Cymal, Ethylvanillin, Florhydral, Helional, Heliotropin, Hydroxycitronellal, Koavon, Lauraldehyd, Lyral, Methylnonylacetaldehyd, P. T. Bucinal, Phenylacetaldehyd, Undecylenaldehyd, Vanillin, 2,6,10- Trimethyl-9-undecenal, 3-Dodecen-1-al, alpha-n-Amylzimtaldehyd, 4-Methoxybenzaldehyd, Benzaldehyd, 3-(4-tert-Butylphenyl)-propanal, 2-Methyl-3-(para-methoxyphenyl)propanal, 2-Methyl- 4-(2,6,6-timethyl-2(1 )-cyclohexen-1-yl)butanal, 3-Phenyl-2-propenal, cis-/trans-3,7-Dimethyl- 2,6- octadien-1-al, 3,7-Dimethyl-6-octen-1-al, [(3,7-Dimethyl-6-octenyl)oxy]acetaldehyd, 4-lsopropyl- benzylaldehyd, 1 ,2, 3,4,5,6,7, 8-Octahydro-8,8-dmethyl-2-naphthaldehyd, 2,4-Dimethyl-3- cyclohexen-1-carboxaldehyd, 2-Methyl-3-(isopropylphenyl)propanal, 1-Decanal, Decylaldehyd, 2,6- Dimethyl-5-heptenal, 4-(Tricyclo[ 5.2.1.0(2, 6)]-decyliden-8)-butanal, Octahydro-4,7-methan-1 H- indencarboxaldehyd, 3-Ethoxy-4-hydroxybenzaldehyd, para-Ethyl-alpha,alphadimethyl- hydrozimtaldehyd, alpha-Methyl-3,4-(methylendioxy)-hydrozimtaldehyd, 3,4-Methylendioxy- benzaldehyd, alpha-n-Hexylzimtaldehyd, m-Cymen-7-carboxaldehyd, alpha-Methylphenyl- acetaldehyd, 7-Hydroxy-3,7-dimethyloctanal, Undecenal, 2,4,6-Trimethyl-3-cyclohexen-1- carboxaldehyd, 4-(3)(4-Methyl-3-pentenyl)-3-cyclohexencarboxaldehyd, 1-Dodecanal, 2,4- Dimethylcyclohexen-3-carboxaldehyd, 4-(4-Hydroxy-4-methylpentyl)-3-cylohexen-1-carboxaldehyd, 7-Methoxy-3,7-dimethyloctan-1-al 2-Methylundecanal, 2-Methyldecanal, 1-Nonanal, 1-Octanal, 2,6,10-Trimethyl-5,9-undecadienal, 2-Methyl- 3-(4-tert-butyl)propanal, Dihydrozimtaldehyd, 1- Methyl-4-(4-methyl-3-pentenyl)-3-cyclohexen-1-carboxaldehyd, 5- oder 6-Methoxyhexahydro-4,7- methanindan-1- oder -2-carboxaldehyd, 3,7-Dimethyloctan-1-al, 1-Undecanal, 10-Undecen-1-al, A- Hydroxy-3-methoxybenzaldehyd, 1-Methyl-3-(4-methylpentyl)-3-cyclohexencarboxaldehyd, 7- Hydroxy-3,7-dimethyl-octanal, trans-4-Decenal, 2,6-Nonadienal, para-Tolylacetaldehyd, A- Methylphenylacetaldehyd, 2-Methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-butenal, ortho- Methoxyzimtaldehyd, 3,5,6-Trimethyl-3-cyclohexencarboxaldehyd, 3,7-Dimethyl-2-nnethylen-6- octenal, Phenoxyacetaldehyd, 5,9-Dimethyl-4,8-decadienal, Päonienaldehyd (6,10-Dimethyl-3-oxa- 5,9-undecadien-1-al), Hexahydro- 4,7-methanindan-1-carboxaldehyd, 2-Methyloctanal, alpha- Methyl-4-(1-methylethyl)benzolacetaldehyd, 6,6-Dimethyl-2-norpinen-2-propionaldehyd, para- Methylphenoxyacetaldehyd, 2-Methyl-3-phenyl-2-propen- 1-al 3,5,5-Trimethylhexanal, Hexahydro- 8,8-dimethyl-2-naphthaldehyd, 3-Propylbicyclo[ 2.2.1]-hept-5-en-2-carbaldehyd, 9-Decenal, 3- Methyl-5-phenyl-1-pentanal, Methylnonylacetaldehyd, Hexanal, trans-2-Hexenal, 1-p-Menthen-q- carboxaldehyd oder Mischungen davon.4. Composition according to one of claims 1 to 3, characterized in that as component (a) a fragrance aldehyde is used, selected from Adoxal, Anisaldehyd, Cymal, Ethylvanillin, Florhydral, Helional, Heliotropin, Hydroxycitronellal, Koavon, Lauraldehyd, Lyral, Methylnonylacetaldehyd , PT Bucinal, phenylacetaldehyde, undecylenealdehyde, vanillin, 2,6,10-trimethyl-9-undecenal, 3-dodecene-1-al, alpha-n-amylcinnamaldehyde, 4-methoxybenzaldehyde, benzaldehyde, 3- (4-tert-butylphenyl ) -propanal, 2-methyl-3- (para-methoxyphenyl) propanal, 2-methyl-4- (2,6,6-timethyl-2 (1) -cyclohexen-1-yl) butanal, 3-phenyl-2 -propenal, cis- / trans-3,7-dimethyl-2,6-octadiene-1-al, 3,7-dimethyl-6-octene-1-al, [(3,7-dimethyl-6-octenyl) oxy] acetaldehyde, 4-isopropylbenzylaldehyde, 1,2,3,4,5,6,7,8-octahydro-8,8-dimethyl-2-naphthaldehyde, 2,4-dimethyl-3-cyclohexene-1 carboxaldehyde, 2-methyl-3- (isopropylphenyl) propanal, 1-decanal, decyl aldehyde, 2,6-dimethyl-5-heptenal, 4- (tricyclo [5.2.1.0 (2, 6)] decylidene-8) -butanal , Oc tahydro-4,7-methane-1H-indenecarboxaldehyde, 3-ethoxy-4-hydroxybenzaldehyde, para-ethyl-alpha, alphadimethylhydrocinnamaldehyde, alpha-methyl-3,4- (methylenedioxy) -hydrocinnamaldehyde, 3,4-methylenedioxy benzaldehyde, alpha-n-hexylcinnamaldehyde, m-cymene-7-carboxaldehyde, alpha-methylphenylacetaldehyde, 7-hydroxy-3,7-dimethyloctanal, undecenal, 2,4,6-trimethyl-3-cyclohexene-1-carboxaldehyde , 4- (3) (4-Methyl-3-pentenyl) -3-cyclohexenecarboxaldehyde, 1-dodecanal, 2,4-dimethylcyclohexene-3-carboxaldehyde, 4- (4-hydroxy-4-methylpentyl) -3-cylohexene 1-carboxaldehyde, 7-methoxy-3,7-dimethyloctan-1-al 2-methylundecanal, 2-methyldecanal, 1-nonanal, 1-octanal, 2,6,10-trimethyl-5,9-undecadienal, 2-methyl - 3- (4-tert-butyl) propanal, dihydrocinnamaldehyde, 1-methyl-4- (4-methyl-3-pentenyl) -3-cyclohexene-1-carboxaldehyde, 5- or 6-methoxyhexahydro-4,7-methanindane 1- or 2-carboxaldehyde, 3,7-dimethyloctan-1-al, 1-undecanal, 10-undecene-1-al, A-hydroxy-3-methoxybenzaldehyde, 1-methyl-3- (4-methylpentyl) -3-cyclohexencarboxalde hyd, 7-hydroxy-3,7-dimethyl-octanal, trans-4-decenal, 2,6-nonadienal, para-tolylacetaldehyde, A-methylphenylacetaldehyde, 2-methyl-4- (2,6,6-trimethyl-1 cyclohexen-1-yl) -2-butenal, ortho Methoxycinnamaldehyde, 3,5,6-trimethyl-3-cyclohexenecarboxaldehyde, 3,7-dimethyl-2-methylene-6-octenal, phenoxyacetaldehyde, 5,9-dimethyl-4,8-decadienal, peonyaldehyde (6,10-dimethyl) 3-oxa-5,9-undecadiene-1-al), hexahydro-4,7-methanindane-1-carboxaldehyde, 2-methyl-octanal, alpha-methyl-4- (1-methylethyl) -benzylacetaldehyde, 6,6-dimethyl 2-norpinen-2-propionaldehyde, para-methylphenoxyacetaldehyde, 2-methyl-3-phenyl-2-propene-1-al 3,5,5-trimethylhexanal, hexahydro-8,8-dimethyl-2-naphthaldehyde, 3-propylbicyclo [2.2.1] hept-5-en-2-carbaldehyde, 9-decenal, 3-methyl-5-phenyl-1-pentanal, methylnonylacetaldehyde, hexanal, trans-2-hexenal, 1-p-menthene-q- carboxaldehyde or mixtures thereof. 5. Mittel gemäß einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, dass die Komponente (b) in Mengen von 0,001 Gew.-% bis 3 Gew.-% in dem Mittel enthalten ist, bezogen auf das gesamte Mittel.5. Composition according to one of claims 1 to 4, characterized in that the component (b) in amounts of 0.001 wt .-% to 3 wt .-% is contained in the agent, based on the total agent. 6. Mittel gemäß einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, dass es 0,001 Gew.-% bis 3 Gew.-% Duftaldehyde enthält, Gew.-% bezogen auf das gesamte Mittel.6. Composition according to one of claims 1 to 5, characterized in that it contains 0.001 wt .-% to 3 wt .-% fragrance aldehydes, wt .-% based on the total agent. 7. Mittel gemäß einem der Ansprüche 1 bis 6, dadurch gekennzeichnet, dass das Verhältnis von Komponente (a) zu Komponente (b) 25:1 bis 1 :5 beträgt.7. Composition according to one of claims 1 to 6, characterized in that the ratio of component (a) to component (b) is 25: 1 to 1: 5. 8. Mittel gemäß einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, dass die gesamte Riechstoffmenge des Mittels 0,01 bis 10 Gew.-% beträgt.8. Composition according to one of claims 1 to 7, characterized in that the total amount of fragrance of the agent is 0.01 to 10 wt .-%. 9. Mittel nach einem der Ansprüche 1-8, dadurch gekennzeichnet, dass es in fester Form vorliegt, vorzugsweise in Pulverform.9. Composition according to one of claims 1-8, characterized in that it is in solid form, preferably in powder form. 10. Mittel nach einem der Ansprüche 1-8, dadurch gekennzeichnet, dass es in flüssiger Form vorliegt, vorzugsweise in Gelform.10. Composition according to one of claims 1-8, characterized in that it is in liquid form, preferably in gel form. 11. Mittel nach einem der Ansprüche 1-10, dadurch gekennzeichnet, dass es zumindest 5 Gew.-%, vorzugsweise zumindest 8 Gew.-%, insbesondere zumindest 10 Gew.-% Tensid enthält, insbesondere Aniontensid und/oder Niotensid.11. Composition according to one of claims 1-10, characterized in that it contains at least 5 wt .-%, preferably at least 8 wt .-%, in particular at least 10 wt .-% surfactant, in particular anionic surfactant and / or nonionic surfactant. 12. Textilreinigungs- oder konditionierverfahren, bei welchem das zu reinigende Textil einer Textilwäsche unter Einsatz eines Wasch-, Reinigungs- oder Pflegemittels nach einem der Ansprüche 1-11 unterworfen wird, insbesondere in einer automatischen Waschmaschine. 12. textile cleaning or conditioning method in which the textile to be cleaned is subjected to a textile washing using a washing, cleaning or care agent according to any one of claims 1-11, in particular in an automatic washing machine. 13. Verwendung eines Wasch-, Reinigungs- oder Pflegemittels nach einem der Ansprüche 1-12 zum Reinigen und/oder Konditionieren von textilen Flächengebilden, insbesondere in einer automatischen Waschmaschine.13. Use of a washing, cleaning or care agent according to any one of claims 1-12 for cleaning and / or conditioning of textile fabrics, in particular in an automatic washing machine. 14. Verwendung von (ggf. substituiertem) Ethylendiamin und/oder (ggf. substituiertem) Propylendiamin als separat zugegebene Komponente in riechstoff haltigen Wasch-, Reinigungsoder Pflegemitteln, welche Duftstoffaldehyd enthalten, zur Verlängerung der Duftwirkung des Wasch-, Reinigungs- oder Pflegemittels.14. Use of (optionally substituted) ethylenediamine and / or (optionally substituted) propylenediamine as a separately added component in perfume-containing washing, cleaning or care products containing fragrance aldehyde, to extend the fragrance effect of the washing, cleaning or care agent. 15. Verwendung von (ggf. substituiertem) Ethylendiamin und/oder (ggf. substituiertem) Propylendiamin als separat zugegebene Komponente in riechstoffhaltigen Wasch-, Reinigungsoder Pflegemitteln, welche Duftstoffaldehyd enthalten, zur Erzielung eines lange anhaltenden Frischegeruches bei der Anwendung des Wasch-, Reinigungs- oder Pflegemittels. 15. Use of (optionally substituted) ethylenediamine and / or (optionally substituted) propylenediamine as a separately added component in perfume-containing detergents, cleaners or conditioners which contain fragrance aldehyde to obtain a long-lasting refreshing odor when using the washing, cleaning or care products.
PCT/EP2010/054918 2009-06-09 2010-04-15 Odor-imparting detergent, cleaning or care product Ceased WO2010142480A1 (en)

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DE200910026855 DE102009026855A1 (en) 2009-06-09 2009-06-09 Scented washing, cleaning or care products
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WO2012139912A1 (en) 2011-04-13 2012-10-18 Firmenich Sa Equilibrated dynamic mixtures to control the release of perfuming aldehydes and ketones

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EP0011499A1 (en) * 1978-11-17 1980-05-28 Unilever Plc Liquid formulations for depositing perfumes on fabric surfaces
WO2003033636A1 (en) * 2001-10-19 2003-04-24 The Procter & Gamble Company Benefit agent delivery systems
DE102005062175A1 (en) * 2005-12-23 2007-06-28 Henkel Kgaa Detergent- or cleaning agent, useful e.g. in liquid or gel form for flushing toilets and hard surface cleaning, comprises cyclic aminal
US20070232507A1 (en) * 1998-07-10 2007-10-04 The Procter & Gamble Company Attention: Chief Patent Counsel Amine reaction compounds comprising one or more active ingredient

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EP0011499A1 (en) * 1978-11-17 1980-05-28 Unilever Plc Liquid formulations for depositing perfumes on fabric surfaces
US20070232507A1 (en) * 1998-07-10 2007-10-04 The Procter & Gamble Company Attention: Chief Patent Counsel Amine reaction compounds comprising one or more active ingredient
WO2003033636A1 (en) * 2001-10-19 2003-04-24 The Procter & Gamble Company Benefit agent delivery systems
DE102005062175A1 (en) * 2005-12-23 2007-06-28 Henkel Kgaa Detergent- or cleaning agent, useful e.g. in liquid or gel form for flushing toilets and hard surface cleaning, comprises cyclic aminal

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012139912A1 (en) 2011-04-13 2012-10-18 Firmenich Sa Equilibrated dynamic mixtures to control the release of perfuming aldehydes and ketones
US9212335B2 (en) 2011-04-13 2015-12-15 Firmenich Sa Equilibrated dynamic mixtures to control the release of perfuming aldehydes and ketones

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