DE102007023805A1 - Textile care agent comprises polycarbonate, polyurethane and/or polyurea polyorganosiloxane compounds comprising carbonyl structural element - Google Patents

Abstract

Textile care agent (A) comprises polycarbonate-, polyurethane- and/or a polyurea polyorganosiloxane compounds comprising at least a carbonyl structural element (I) or their acid addition compounds and/or salts. Textile care agent (A) comprises polycarbonate-, polyurethane- and/or a polyurea polyorganosiloxane compounds comprising at least a carbonyl structural element of formula (-Y 1>-A-(C=O)-A-) (I) or their acid addition compounds and/or salts. Either A : S, O or NR 1>; and Y 1>bivalent to polyvalent, preferably tetravalent, optionally saturated or aromatic up to 1000C hydrocarbon containing one or more NR 2>, (N +>R 2>R 3>) (both preferred), O, (CO), NH, 2-1000 polyorganosiloxane unit with silicon atom (optionally substituted), preferably oligoethoxy and/or oligopropoxy (where its oligomerization degree is preferably 2-60) or oligoethylene imine(where its oligomerization degree is preferably 10-150000); or Y 1>A : nitrogen containing heterocyclic ring; R 1>H, optionally saturated or aromatic up to 40C hydrocarbon containing one or more O, (CO), NH, NR 2>, preferably oligoethoxy and/or oligopropoxy (where its oligomerization degree is preferably 2-60) or oligoethylene imine (where its oligomerization degree is preferably 10-150000); R 2>optionally saturated, aromatic up to 40C hydrocarbon containing one or more O, (CO), NH, preferably oligoethoxy and/or oligopropoxy (where its oligomerization degree is preferably 2-60) or oligoethylene imine (where its oligomerization degree is preferably 10-150000); and R 3>optionally saturated, aromatic up to 100C hydrocarbon containing one or more O, (CO), NH, a bivalent residue, which form cyclic structures within the Y 1>, preferably oligoethoxy and/or oligopropoxy (where its oligomerization degree is preferably 2-60) or oligoethylene imine (where its oligomerization degree is preferably 10-150000). Provided that: in formula (I) A, Y 1>, R 1>, R 2>, R 3> are not same, when at least one of the remainders of Y 1> is polyorganosiloxane unit with 2-1000 silicon atom. Independent claims are included for: (1) (A) comprising (1,3)dioxolan-2-one compound of formula (IV) or (1,3)-diazepan-2-one compound of formula (V) and/or polymer, where the polymer is obtained by the reaction of a polymer substrate (that modifies the functional groups of hydroxy-, primary and secondary amino- group) with (IV) or (V); and (2) a method for reducing the lint build up of the textile material comprising contacting the textile material and the textile care product in a textile purification process and/or a textile drying process. [Image] .

Description

The The invention relates to the use of certain cyclic carbonates or ureas or derivatives thereof for the reduction of Creasing, improving the ironing properties as well improving the elasticity of treated therewith Laundry and textile care products containing such active ingredients.

The modern textile cleaning makes high demands on the to be cleaned Laundry. Such is the frequent washing of clothes in a washing machine and that yourself subsequent drying in a tumble dryer associated with a high mechanical stress on the tissue. The frictional forces often lead to damage of the textile fabric, recognizable by a lint and pilling. With every wash or dry, but also by wearing the garments finds another Abrasion and / or breakage of tiny fibers on the surface the textile surface fabric instead. The conventional ones Textile detergents are able to damage this Do not prevent tissue or just try, already existing To eliminate textile damage.

The international patent application WO 99/16956 A1 suggests the elimination of lint or pills through the use of cellulases. The cellulases thereby break off the microfibers protruding from the textile fabrics and thus ensure a smooth and therefore pilling-free textile surface.

Another major disadvantage of the mechanical stress on textile fabrics is the formation of unwanted wrinkled textile surfaces from the consumer and the formation of rough surfaces. Both the rough textile surfaces and the resulting creasing of the fabrics (their significant worsening of the sliding properties of irons or other textile flattening devices.) The expense of flattening rough and crumpled textiles is not only due to a greater effort, but also to a considerable amount of additional time In the prior art, solutions for improving the ironing properties of laundered textiles are found mainly in the field of aftertreatment agents WO 00/77134 discloses the use of oxidized polyolefins in softener formulations to improve ironing properties.

The use of celluloses, hydrogels and acrylic acid polymers as lint reduction components in textile treatment agents is known from the German patent application DE 102 03 192 A1 known.

Surprisingly has now been found that the use of certain reactive cyclic carbonates or ureas and derivatives of these in the washing process a significant improvement in fiber and textile properties leads.

worin
R für C₁-C₁₂-Alkylen steht;
k für eine Zahl größer als 0 steht,
X für CO-CH=CH₂, CO-C(CH₃)= CH₂, CO-O-Aryl, C₂-C₆-Alkylen-SO₂-CH=CH₂, oder CO-NH-R¹ steht; und R¹ für C₁-C₃₀-Alkyl, C₁-C₃₀-Halogenalkyl, C₁-C₃₀-Hydroxyalkyl, C₁-C₆-Alkyloxy-C₁-C₃₀-alkyl, C₁-C₆-Alkylcarbonyloxy-C₁-C₃₀-alkyl, Amino-C₁-C₃₀-alkyl, Mono- oder Di(C₁-C₆-alkyl)amino-C₁-C₃₀-alkyl, Ammonio-C₁-C₃₀-alkyl, Polyoxyalkylen-C₁-C₃₀-alkyl, Polysiloxanyl-C₁-C₃₀-alkyl, (Meth)acryloyloxy-C₁-C₃₀-alkyl, Sulfono-C₁-C₃₀-alkyl, Phosphono-C₁-C₃₀-alkyl, Di(C₁-C₆-alkyl)phosphono-C₁-C₃₀-alkyl, Phosphonato-C₁-C₃₀-alkyl, Di(C₁-C₆-alkyl)phosphonato-C₁-C₃₀-alkyl oder einen Saccharidrest steht,
wobei in Formel IX diese Bedeutung nur dann hat, wenn k für 1 steht, oder
X für
(i) den Rest eines Polyamins, an das der in Klammern stehende Formelteil über (CO)NH-Gruppen gebunden ist, oder
(ii) ein polymeres Gerüst, an das der in Klammern stehende Formelteil über (CO)-, NH-C₂-C₆-Alkylen-O(CO)- oder (CO)-O-C₂-C₆-Alkylen-O(CO)-Gruppen gebunden ist, oder (iii) ein polymeres Gerüst, an das der in Klammern stehende Formelteil über (CO)-Polysiloxanyl-C₁-C₃₀-alkyl-Gruppen gebunden ist,
steht, wenn k für eine Zahl von mehr als 1 steht,
und Polymeren, welche erhältlich sind durch Umsetzung eines polymeren Substrates, das über funktionelle Gruppen verfügt, welche unter Hydroxygruppen, primären und sekundären Aminogruppen ausgewählt sind, mit einer Verbindung der allgemeinen Formeln I oder II.The present invention therefore relates, in a first embodiment, to a fabric care composition containing an active substance selected from the compounds of the general formulas I or II,

wherein
R is C ₁ -C ₁₂ alkylene;
k is a number greater than 0,
X is CO-CH = CH ₂ , CO-C (CH ₃ ) = CH ₂ , CO-O-aryl, C ₂ -C ₆ -alkylene-SO ₂ -CH = CH ₂ , or CO-NH-R ¹ ; and R ^{1 is} C ₁ -C ₃₀ -alkyl, C ₁ -C ₃₀ -haloalkyl, C ₁ -C ₃₀ -hydroxyalkyl, C ₁ -C ₆ -alkyloxy-C ₁ -C ₃₀ -alkyl, C ₁ -C ₆ - Alkylcarbonyloxy-C ₁ -C ₃₀ -alkyl, amino-C ₁ -C ₃₀ -alkyl, mono- or di (C ₁ -C ₆ -alkyl) amino-C ₁ -C ₃₀ -alkyl, ammonio-C ₁ -C ₃₀ alkyl, polyoxyalkylene C ₁ -C ₃₀ alkyl, polysiloxanyl C ₁ -C ₃₀ alkyl, (meth) acryloyloxy C ₁ -C ₃₀ alkyl, sulfono C ₁ -C ₃₀ alkyl, phosphonoC ₁ C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphono C ₁ -C ₃₀ alkyl, phosphonato C ₁ -C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphonato C ₁ C ₃₀ alkyl or a saccharide radical,
where in formula IX this meaning has only if k is 1, or
X for
(i) the residue of a polyamine to which the parenthesized part of the formula is linked via (CO) NH groups, or
(ii) a polymeric backbone to which the parenthesized part of the formula is attached via (CO) -, NH-C ₂ -C ₆ -alkylene-O (CO) - or (CO) -OC ₂ -C ₆ -alkylene-O ( Or (iii) a polymeric backbone to which the parenthesized formula portion is attached via (CO) polysiloxanyl-C ₁ -C ₃₀ alkyl groups;
stands if k stands for a number of more than 1,
and polymers obtainable by reacting a polymeric substrate having functional groups selected from hydroxy groups, primary and secondary amino groups with a compound of general formulas I or II.

To The suitable polymeric substrates include in particular Polyvinyl alcohols, polyalkylene amines such as polyethyleneimines, polyvinylamines, Polyallylamines, polyethylene glycols, chitosan, polyamide-epichlorohydrin resins, Polyaminostyrenes, with aminoalkyl groups terminal or as a side group substituted polysiloxanes such as polydimethylsiloxanes, peptides, polypeptides, and proteins and mixtures thereof.

Particularly preferred polymeric substrates are selected from polyethyleneimines having molecular weights in the range from 5,000 to 100,000, in particular 15,000 to 50,000, compounds of the formula NH ₂ - [CH ₂ ] _m - (Si (CH ₃ ) ₂ O) _n -Si (CH ₃ ) ₂ - [CH ₂ ] _o -R ', where m = 1 to 10, preferably 1 to 5, particularly preferably 1 to 3, where n = 1 to 50, preferably 30 to 50, wherein 0 = 0 to 10, preferably 1 to 5, more preferably 1 to 3 and wherein R '= H, C _1-22 alkyl, an amino or ammonium group, and / or compounds of the formula NH ₂ - [CH ( CH ₃ ) -CH ₂ O] ₁ - [CH ₂ -CH ₂ O] _m [CH ₂ -CH (CH ₃ ) O] _n -R ", where 1, m and n are independently from 0 to 50 with the proviso that the sum is 1 + m + n = 5 to 100, in particular 10 to 50, preferably 10 to 30, particularly preferably 10 to 20, and R '' = H, a C _1-22 -alkyl-, C _1-22 aminoalkyl or C _1-22 ammonium alkyl group, and mixtures thereof.

Under The polymers are those which are preferred by reacting the polymeric substrate with a compound of the general formulas I are available with k = 1 or II. Further preferred are those polymers which, by reaction of the polymeric substrate with respect to its content of hydroxyl groups, primary and secondary amino groups equal molar amounts Compound of the general formulas I with k = 1 or II available are.

The compound of formula 1 is preferably selected from
4-phenyloxycarbonyloxymethyl-2-oxo-1,3-dioxolane,
4- (4-Phenyloxycarbonyloxy) butyl-2-oxo-1,3-dioxolane,
2-oxo-1,3-dioxolan-4-yl-methyl,
2-oxo-1,3-dioxolan-4-yl-methyl,
4- (2-oxo-1,3-dioxolan-4-yl) butyl acrylate,
4- (2-oxo-1,3-dioxolan-4-yl) -butyl methacrylate and
4- (Vinylsulfonylethyloxy) butyl-2-oxo-1,3-dioxolane.

The preparation of compounds of the general formulas I and II and their reaction with polymeric substrates are described in the international patent application WO 2005/058863 described.

Preferred polymers obtainable from compounds of the general formula (I) or (II) are siloxane-EO block copolymers which are polycarbonate and / or polyurethane-polyorganosiloxane compounds containing at least one structural element of the formula (III): -AYA- (CO) -OZ- (CH 2 OH) -ZO- (CO) - (III), wherein A is selected from -O-, -S- and -NR ² -, Y is selected from di- to polyvalent, especially tetravalent, straight-chain, cyclic or branched, saturated, unsaturated or aromatic, substituted or unsubstituted hydrocarbon radicals having up to 1000 Carbon atoms which may contain one or more groups selected from -O-, - (CO) -, -NH-, -NR ² -, - (N ⁺ R ³ R ⁴ ) - and a polyorganosiloxane unit having 2 to 1000 silicon atoms, Z is selected from the divalent, straight-chain, cyclic or branched, saturated or unsaturated, optionally substituted hydrocarbon radicals having 1 to 12 carbon atoms,
R ^{2 is} hydrogen or a straight-chained, cyclic or branched, saturated, unsaturated or aromatic hydrocarbon radical having up to 40 carbon atoms and having one or more groups selected from May contain -O-, - (CO) -, -NH- and -NR ³ -,
R ^{3 is} a straight-chain, cyclic or branched, saturated, unsaturated or aromatic hydrocarbon radical having up to 40 carbon atoms, which may contain one or more groups selected from -O-, - (CO) - and -NH-,
R ^{4 is} a straight-chain, cyclic or branched, saturated, unsaturated or aromatic hydrocarbon radical having up to 100 carbon atoms, which may contain one or more groups selected from -O-, - (CO) - and -NH-, or a bivalent radical is that forms cyclic structures within the radical Y, or one or both of Y may form adjacent radicals Y with the radical Y between them, a nitrogen-containing heterocyclic radical,
and in the entire compound not all radicals A or Y or Z or R ² or R ³ or R ⁴ given in formula (III) must be identical, with the proviso that at least one of the radicals Y in the entire compound a polyorganosiloxane unit having 2 to 1000 silicon atoms,
and their acid addition compounds and / or salts. The polycarbonate and / or polyurethane-polyorganosiloxane compound preferably has the structural element of the formula (III) several times in succession, the multiply occurring in each case corresponding radicals A or Y or Z or R ² or R ³ or R ^{4 may be the} same or different.

Of the Term acid addition compound means salt-like Compounds formed by protonation of basic groups in the molecule, in particular the optionally present amino groups, for example by reaction with inorganic or organic acids can be obtained. These acid addition compounds can be used as such or under conditions of use optionally form compounds defined above.

If the polycarbonate and / or polyurethane polyorganosiloxane compound contains moieties - (N ⁺ R ³ R ⁴ ) -, conventional counter anion ions, such as halide, hydroxide, sulfate, carbonate, are present to ensure charge neutrality.

The polyorganosiloxane structural element present in the polycarbonate and / or polyurethane-polyorganosiloxane compounds is preferably the structure - (R ⁵ ₂ SiO) _p - (SiR ⁵ ₂ ) -, where R ^{5 is} a straight-chain, cyclic or branched, saturated, unsaturated or aromatic hydrocarbon radical having up to 20 carbon atoms, and p = 1 to 999. Preferably, the polycarbonate and / or polyurethane-polyorganosiloxane compounds contain on average at least two, preferably at least three of said polyorganosiloxane structural elements. R ⁵ is preferably a straight-chain or cyclic or branched, saturated or unsaturated or aromatic C ₁ - to C ₂₀ -, in particular C ₁ - to C ₉ -hydrocarbon radical, particularly preferably methyl or phenyl, and p is in particular 1 to 199, particularly preferred 1 to 99. In a preferred embodiment, all R ^{5 are the} same.

In a further embodiment, in the polycarbonate and / or polyurethane-polyorganosiloxane compound used according to the invention at least one of the Y units according to the structural element of the formula (III) has a grouping -NR ³ - and / or at least one of the Y units according to the structural element of Formula (III) a grouping - (N ⁺ R ³ R ⁴ ) - on. R ³ and R ⁴ are preferably methyl groups.

A further embodiment relates to the multiple regular occurrence of -O-groupings in at least one of the units Y, R ² , R ³ and / or R ⁴ , preferably in the form of oligoethoxy and / or oligopropoxy groups, their degrees of oligomerization preferably being in the range from 2 to 60 are.

preferred used in the invention polycarbonate and / or Polyurethane-polyorganosiloxane compounds are linear, that is There, all Y units in formula (III) are each bivalent radicals. However, according to the invention, branched polycarbonate and / or polyurethane-polyorganosiloxane compound wherein at least one of the radicals Y is tri- or polyvalent, preferably tetravalent is, so that branched structures with repetitive structures from structural elements of the formula (III) form.

The Preparation of compounds with structural elements of the formula (III) starting from reactive cyclic carbonates or ureas of Formulas (I) or (II) is in the same day of the Momentive Performance Material submitted German patent application disclosed.

In the context of this invention, textile care agents are understood as meaning both pretreatment agents and conditioning agents for textile fabrics, such as mild detergents and post-treatment agents, such as fabric softeners. Conditioning is to be understood as the avivating treatment of textile fabrics, fabrics, yarns and fabrics. By conditioning the textiles positive egg properties such as improved softness, increased gloss and color brilliance, as well as the reduction of creasing and static charge.

At the Use of inventive agent or in the use according to the invention is in particular prevents the wrinkling of textiles through the washing and / or drying process, the ironing properties of the textile are improved and the "leaching" of textiles during washing is considerably reduced. In addition, especially in synthetic fibers, the otherwise hardly absorbs moisture such as perspiration can, the water intake ability by the Use of inventive agent or significant by the use according to the invention increases and thereby the wearing feeling of the textiles much more pleasant.

The Fabric care agents according to the invention can both in solid form, for example as a powder, granules, extrudate, pressed and / or melted shaped body as a tablet, or in liquid form, for example as a dispersion, Suspension, emulsion, solution, microemulsion, gel or paste available. In a preferred embodiment of the invention they are liquid. A textile care product can in extreme cases consist solely of the above-mentioned active substance but preferably further in textile treatment agents usual Components that are not unreasonable during storage and use Way negative interact with the said drug. An inventive Agent preferably contains 0.01 wt .-% to 5 wt .-%, in particular 0.1 wt .-% to 2 wt .-% of the above-defined active ingredient.

In a preferred embodiment of the present invention contain the fabric care agents in addition to the defined Active agent complexing agent. It's surprising shown that in particular organic, advantageously water-soluble, complexing agent particularly good in the Incorporate textile care agents according to the invention and in particular together with the invention to be used Cellulose ethers the textile care products, including in particular the liquid preparations, increased stability gives. The complexing agents improve the stability the agent and protect against, for example, by heavy metals catalyzed decomposition of certain ingredients of washing-active formulations. Together with the invention to be used Cellulose ethers contribute to the inhibition of incrustations. The group of complexing agents includes, for example, the salts, in particular the alkali metal salts of nitrilotriacetic acid (NTA) and their derivatives and alkali metal salts of anionic Polyelectrolytes such as polymaleates and polysulfonates. Furthermore are Citric acid, adipic acid, succinic acid, glutaric acid, malic acid, Tartaric acid, maleic acid, fumaric acid, sugar acids, Aminocarboxylic acids and their derivatives as well Mixtures of these suitable. Preferred compounds include in particular organophosphonates such as, for example, 1-hydroxyethane-1,1-diphosphonic acid (HEDP), aminotri (methylenephosphonic acid) (ATMP), diethylenetriamine-penta (methylenephosphonic acid) (DTPMP or DETPMP) as well as 2-phosphonobutane-1,2,4-tricarboxylic acid (PBS-AM), which are mostly in the form of their ammonium or alkali metal salts be used. Particularly preferred in the context of the present Invention is the citric acid and / or its alkali metal salts, for example, sodium citrate and / or potassium citrate. In a preferred embodiment The fabric care agents contain complexing agents in an amount to 20 wt .-%, preferably from 0.01 to 15 wt .-%, particularly preferably from 0.1 to 10 and in particular from 0.3 to 5.0 wt .-%, advantageously from 1.5 to 3 wt .-%, each based on the total agent.

In a preferred embodiment, the inventive Textile care products additionally nonionic surfactants. By The use of nonionic surfactants is not only the washing performance the agent according to the invention increases, but additionally the dispersion and homogeneous distribution of the active ingredient to be used according to the invention supported.

As nonionic surfactants are preferably alkoxylated, advantageously ethoxylated and / or propoxylated, in particular primary alcohols having preferably 8 to 18C atoms and an average of 1 to 12 moles of ethylene oxide (EO) and / or 1 to 10 moles of propylene oxide (PO) per mole of alcohol used , Particular preference is given to C ₈ -C ₁₆ -alcohol alkoxylates, advantageously ethoxylated and / or propoxylated C ₁₀ -C ₁₅ -alcohol alkoxylates, in particular C ₁₂ -C ₁₄ -alcohol alkoxylates, having a degree of ethoxylation of between 2 and 10, preferably between 3 and 8, and / or a degree of propoxylation between 1 and 6, preferably between 1.5 and 5. The alcohol radical may preferably be linear or more preferably methyl-branched in the 2-position or contain linear and methyl-branched radicals in the mixture, as they are usually present in Oxoalkoholresten. In particular, however, alcohol ethoxylates with linear radicals of alcohols of native origin having 12 to 18 carbon atoms, for. From coconut, palm, tallow or oleyl alcohol, and on average from 2 to 8 EO per mole of alcohol. The preferred ethoxylated alcohols include, for example, C _12-14 alcohols with 3 EO or 4 EO, C _9-11 alcohols with 7 EO, C _13-15 alcohols with 3 EO, 5 EO, 7 EO or 8 EO, C _12-18 -alcohols with 3 EO, 5 EO or 7 EO and mixtures of these, such as mixtures of C _12-14 -alcohol with 3 EO and C _12-18 -alcohol with 5 EO. The indicated degrees of ethoxylation and propoxylation represent statistical averages which may be an integer or a fractional number for a particular product. Preferred alcohol ethoxylates and propoxylates have a narrow homolog distribution (narrow range ethoxylates / propoxylates, NRE / NRP). In addition to these nonionic surfactants, fatty alcohols with more than 12 EO can also be used. Examples include tallow fatty alcohol with 14 EO, 25 EO, 30 EO or 40 EO.

Farther suitable are alkoxylated amines, advantageously ethoxylated and / or propoxylated, especially primary and secondary Amines having preferably 1 to 18 carbon atoms per alkyl chain and average 1 to 12 moles of ethylene oxide (EO) and / or 1 to 10 moles of propylene oxide (PO) per mole of amine.

As particularly advantageous, especially for use in non-aqueous formulations according to the invention, the end-capped alkoxylated fatty amines and fatty alcohols have been found. The terminal hydroxy groups of the fatty alcohol alkoxylates and fatty amine alkoxylates are etherified by C ₁ -C ₂₀ -alkyl groups, preferably methyl or ethyl groups, in the end-capped fatty alcohol alkoxylates and fatty amine alkoxylates.

In addition, as further nonionic surfactants and alkyl glycosides of the general formula RO (G) _x , z. B. be used as compounds, especially with anionic surfactants, in which R is a primary straight-chain or methyl-branched, especially methyl-branched in the 2-position aliphatic radical having 8 to 22, preferably 12 to 18C atoms and G is the symbol for a glycose unit with 5 or 6C atoms, preferably for glucose. The degree of oligomerization x, which indicates the distribution of monoglycosides and oligoglycosides, is any number between 1 and 10; preferably x is 1.2 to 1.4.

Another class of preferred nonionic surfactants used either as the sole nonionic surfactant or in combination with other nonionic surfactants are alkoxylated, preferably ethoxylated or ethoxylated and propoxylated fatty acid alkyl esters, preferably having from 1 to 4 carbon atoms in the alkyl chain, especially fatty acid methyl esters as they are For example, in the Japanese patent application JP 58/217598 are described or preferably according to the in the international patent application WO 90/13533 be prepared described methods.

When other surfactants are so-called gemini surfactants into consideration. this includes In general, compounds which are two hydrophilic Possess groups and two hydrophobic groups per molecule. These groups are usually by a so-called "spacer" separated from each other. This spacer is usually a carbon chain, which should be long enough that the hydrophilic groups have a sufficient distance to make them independent can act from each other. Draw such surfactants generally characterized by an unusually low critical Micelle concentration and the ability to surface tension to greatly reduce the water out. In exceptional cases However, under the term gemini surfactants, they are not only dimeric, but also understood trimeric surfactants.

Suitable gemini surfactants are, for example, sulfated hydroxy mixed ethers according to the German patent application DE-A-43 21 022 or dimer alcohol bis- and trimeralcohol tris-sulfates and ether sulfates according to the international patent application WO-A-96/23768 , End-capped dimeric and trimeric mixed ethers according to the German patent application DE-A-195 13 391 They are characterized by their bi- and multi-functionality. Thus, the end-capped surfactants mentioned have good wetting properties and are low foaming, so that they are particularly suitable for use in machine washing or cleaning processes.

However, it is also possible to use gemini-polyhydroxy fatty acid amides or poly-polyhydroxy fatty acid amides, as described in international patent applications WO 95/19953 . WO 95/19954 and WO 95/19955 to be discribed.

in der R⁴CO für einen aliphatischen Acylrest mit 6 bis 22 Kohlenstoffatomen, R³ für Wasserstoff, einen Alkyl- oder Hydroxyalkylrest mit 1 bis 4 Kohlenstoffatomen und [Z] für einen linearen oder verzweigten Polyhydroxyalkylrest mit 3 bis 10 Kohlenstoffatomen und 3 bis 10 Hydroxylgruppen steht. Bei den Polyhydroxyfettsäureamiden handelt es sich um bekannnte Stoffe, die üblicherweise durch reduktive Aminierung eines reduzierenden Zuckers mit Ammoniak, einem Alkylamin oder einem Alkanolamin und nachfolgende Acylierung mit einer Fettsäure, einem Fettsäurealkylester oder einem Fettsäurechlorid erhalten werden können.Further suitable surfactants are polyhydroxy fatty acid amides of the following formula

in the R ⁴ CO for an aliphatic acyl radical having 6 to 22 carbon atoms, R ^{3 is} hydrogen, an alkyl or hydroxyalkyl radical having 1 to 4 carbon atoms and [Z] represents a linear or branched polyhydroxyalkyl radical having 3 to 10 carbon atoms and 3 to 10 hydroxyl groups. The polyhydroxy fatty acid amides are known substances which can usually be obtained by reductive amination of a reducing sugar with ammonia, an alkylamine or an alkanolamine and subsequent acylation with a fatty acid, a fatty acid alkyl ester or a fatty acid chloride.

in der R⁵ für einen linearen oder verzweigten Alkyl- oder Alkenylrest mit 7 bis 12 Kohlenstoffatomen, R⁶ für einen linearen, verzweigten oder cyclischen Alkylrest oder einen Arylrest mit 2 bis 8 Kohlenstoffatomen und R⁷ für einen linearen, verzweigten oder cyclischen Alkylrest oder einen Arylrest oder einen Oxy-Alkylrest mit 1 bis 8 Kohlenstoffatomen steht, wobei C₁₄-Alkyl- oder Phenylreste bevorzugt sind und [Z] für einen linearen Polyhydroxyalkylrest steht, dessen Alkylkette mit mindestens zwei Hydroxylgruppen substituiert ist, oder alkoxylierte, vorzugsweise ethoxylierte oder propoxylierte Derivate dieses Restes. [Z] wird vorzugsweise durch reduktive Aminierung eines reduzierten Zuckers erhalten, beispielsweise Glucose, Fructose, Maltose, Lactose, Galactose, Mannose oder Xylose. Die N-Alkoxy- oder N-Aryloxy-substituierten Verbindungen können dann beispielsweise nach der Lehre der internationalen Patentanmeldung WO-A-95/07331 durch Umsetzung mit Fettsäuremethylestern in Gegenwart eines Alkoxids als Katalysator in die gewünschten Polyhydroxyfettsäureamide überführt werden.The group of polyhydroxy fatty acid amides also includes compounds of the following formula

in the R ^{5 is} a linear or branched alkyl or alkenyl radical having 7 to 12 carbon atoms, R ^{6 is} a linear, branched or cyclic alkyl radical or an aryl radical having 2 to 8 carbon atoms and R ^{7 is} a linear, branched or cyclic alkyl radical or a Aryl radical or an oxy-alkyl radical having 1 to 8 carbon atoms, wherein C ₁₄ alkyl or phenyl radicals are preferred and [Z] is a linear polyhydroxyalkyl radical whose alkyl chain is substituted with at least two hydroxyl groups, or alkoxylated, preferably ethoxylated or propoxylated derivatives this rest. [Z] is preferably obtained by reductive amination of a reduced sugar, for example glucose, fructose, maltose, lactose, galactose, mannose or xylose. The N-alkoxy- or N-aryloxy-substituted compounds can then be used, for example, according to the teaching of the international patent application WO-A-95/07331 be converted by conversion with fatty acid methyl esters in the presence of an alkoxide as catalyst into the desired Polyhydroxyfettsäureamide.

For the textile care agent according to the invention has it proved to be advantageous when nonionic surfactants selected from the group of alkoxylated fatty alcohols and / or alkyl glycosides, especially mixtures of alkoxylated Fatty alcohols and alkyl glycosides.

In the Textilpilegemittein invention are located in a preferred embodiment nonionic Surfactants in amounts of up to 35 wt .-%, preferably from 5 to 25 Wt .-%, particularly preferably from 10 to 20 wt .-%, each based on the entire remedy.

Farther can the textile care agents of the invention in addition to or instead of the nonionic surfactants as well contain anionic surfactants. By the use of anionic Surfactants become the soil release behavior of the invention Means significantly increased during the washing process, without the effect of the invention used Cellulose ethers - despite their cationic charge - as Fluff reduction component and anti-crease component essential to impair.

As anionic surfactants, for example, those of the sulfonate type and sulfates are used. The surfactants of the sulfonate type are preferably C _9-13 -alkylbenzenesulfonates, olefinsulfonates, ie mixtures of alkene and hydroxyalkanesulfonates and disulfonates, as are obtained, for example, from C _12-18 -monoolefins having terminal or internal double bonds by sulfonation with gaseous sulfur trioxide and subsequent alkaline or acid hydrolysis of the sulfonation products into consideration. Also suitable are alkanesulfonates which are obtained from C _12-18 alkanes, for example by sulfochlorination or sulfoxidation with subsequent hydrolysis or neutralization. Likewise, the esters of α-sulfo fatty acids (ester sulfonates), z. As the α-sulfonated methyl esters of hydrogenated coconut, palm kernel or tallow fatty acids suitable.

Further Suitable anionic surfactants are sulfated fatty acid glycerol esters. Among fatty acid glycerol esters are the mono-, di- and triesters As well as their mixtures to understand, as in the production through Esterification of a monoglycerine with 1 to 3 moles of fatty acid or in the transesterification of triglycerides with 0.3 to 2 moles of glycerol to be obtained. Preferred sulfated fatty acid glycerol esters are the sulfonation of saturated fatty acids with 6 to 22 carbon atoms, for example caproic acid, Caprylic acid, capric acid, myristic acid, Lauric acid, palmitic acid, stearic acid or behenic acid.

Alk (en) ylsulfates are the alkali metal salts and in particular the sodium salts of the sulfuric monoesters of C ₁₂ -C 18 fatty alcohols, for example coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or the C ₁₀ -C ₂₀ oxo alcohols and those half-esters of secondary alcohols of these chain lengths are preferred. Also preferred are alk (en) ylsulfates of said chain length which contain a synthetic, petrochemical-based straight-chain alkyl radical which is an analogous degradation ver Keep like the adequate compounds based on oleochemical raw materials. Of washing technology interest, the C ₁₂ -C ₁₆ alkyl sulfates and C ₁₂ -C ₁₅ alkyl sulfates and C ₁₄ -C ₁₅ alkyl sulfates are preferred. Also 2,3-alkyl sulfates, which, for example, according to the patents US 3,234,258 or US 5 075 041 are manufactured and can be obtained as commercial products from Shell Oil Company under the name DAN ^®, are suitable anionic surfactants.

The sulfuric acid monoesters of straight-chain or branched C _7-21 -alcohols ethoxylated with from 1 to 6 mol of ethylene oxide, such as 2-methyl-branched C _9-11- alcohols having on average 3.5 mol of ethylene oxide (EO) or C _12-18 . Fatty alcohols containing 1 to 4 EO, which are referred to as fatty alcohol ether sulfates, are suitable and particularly preferred anionic surfactants within the scope of this invention.

Further suitable anionic surfactants are also the salts of alkylsulfosuccinic acid, which are also referred to as sulfosuccinates or as sulfosuccinic acid esters and which are monoesters and / or diesters of sulfosuccinic acid with alcohols, preferably fatty alcohols and in particular ethoxylated fatty alcohols. Preferred sulfosuccinates contain C _8-18 fatty alcohol residues or mixtures of these. Particularly preferred sulfosuccinates contain a fatty alcohol residue derived from ethoxylated fatty alcohols, which by themselves are nonionic surfactants. Again, sulfosuccinates whose fatty alcohol radicals are derived from ethoxylated fatty alcohols with a narrow homolog distribution are particularly preferred. Likewise, it is also possible to use alk (en) ylsuccinic acid having preferably 8 to 18 carbon atoms in the alk (en) yl chain or salts thereof.

When other anionic surfactants are especially soaps into consideration. Suitable examples are the saturated fatty acid soaps, such as the salts of lauric acid, myristic acid, Palmitic acid, stearic acid, hydrogenated erucic acid and behenic acid and in particular natural Fatty acids, e.g. Coconut, palm kernel or tallow fatty acids, derived soap mixtures.

The anionic surfactants including soaps can in the form of their sodium, potassium or ammonium salts and as soluble Salts of organic bases, such as mono-, di- or triethanolamine, are present. The anionic surfactants are preferably in the form of their sodium or potassium salts, especially in the form of the sodium salts. For he inventive non-aqueous However, liquid detergents are the ammonium salts, in particular the salts of organic bases, such as isopropylamine, are preferred.

Another class of anionic surfactants is the class of ether carboxylic acids obtainable by the reaction of fatty alcohol ethoxylates with sodium chloroacetate in the presence of basic catalysts. They have the general formula: R ¹⁰ O- (CH ₂ -CH ₂ -O) _p CH ₂ -COOH with R ¹⁰ = C ₁ -C ₁₈ and p = 0.1 to 20. Ethercarboxylic acids are water hardness insensitive and have excellent surfactant properties ,

The Contain textile cleaners according to the invention in a preferred embodiment, anionic surfactants, preferably selected from the group of fatty alcohol sulfates and / or fatty alcohol ether sulfates and / or alkylbenzenesulfonates and / or Soap.

ever according to the purpose of the textile care agents according to the invention The content of anionic surfactants can vary considerably. Lie the textile care products as mild detergent or aftertreatment agent, For example, as a fabric softener, the amounts are normally below 10% by weight, preferably below 5 wt .-% and in particular below 1 wt .-%, in each case on the entire remedy.

Lie the textile care products as a solid or liquid heavy-duty detergent, for example, as a non-aqueous liquid detergent anionic surfactants in amounts of up to 65% by weight, preferably in amounts of up to 50 wt .-%, particularly preferably in Amounts of from 5 to 35% by weight, in each case based on the total agent, be included.

Farther can the textile care agents of the invention in a preferred embodiment in addition Contain enzymes.

Enzymes support the washing processes in a variety of ways, especially in the removal of poorly bleachable contaminants, such as protein stains. The incorporation of enzymes in detergent formulations, especially in liquid fabric care products, however, often causes problems, since it can lead to incompatibilities with other detergent ingredients, which in turn can cause a loss of activity of the enzymes. Surprisingly, it was found that through the use of The copolymers to be used according to the invention can be used to improve the stability of the enzymes in wash liquor or textile care formulation, in particular in liquid fabric care formulations.

When Enzymes are especially those from the classes of hydrolases as the proteases, esterases, lipases or lipolytic acting Enzymes, amylases, cellulases or other glycosyl hydrolases and mixtures the enzymes mentioned in question. All of these hydrolases carry in the Laundry to remove stains such as protein, grease and or starchy stains and grayness. Cellulases and other glycosyl hydrolases may be over it By removing pilling and microfibrils for color retention and to increase the softness of the textile. to Bleaching or to inhibit color transfer can also Oxireduktasen be used. Particularly well suited from bacterial strains or fungi such as Bacillus subtilis, Bacillus licheniformis, Streptomyceus griseus and Humicola insolens recovered enzymatic agents. Preferably, proteases of the subtilisin type and in particular proteases derived from Bacillus lentus are used. These are enzyme mixtures, for example from protease and amylase or protease and lipase or lipolytic enzymes or protease and cellulase or from cellulase and lipase or lipolytic enzymes or from protease, amylase and lipase or lipolytic enzymes or protease, lipase or lipolytic enzymes and cellulase, but in particular protease and / or lipase-containing mixtures or mixtures with lipolytic enzymes of particular Interest. Examples of such lipolytic acting Enzymes are the known cutinases. Also peroxidases or oxidases have proven to be suitable in some cases. To the suitable amylases include in particular α-amylases, Iso-amylases, pullulanases and pectinases. Being cellulases preferably cellobiohydrolases, endoglucanases and β-glucosidases, which are also called cellobiases, or mixtures of these used. Because different types of cellulase are affected by their CMCase and avicelase activities by targeted mixtures of cellulases the desired Activities are discontinued.

The Enzymes can be adsorbed to carriers or be coated to protect against premature decomposition.

The Containing textile care agents according to the invention in a preferred embodiment, enzymes, preferably selected from the group of proteases and / or amylases and / or cellulases.

Lie the textile care compositions of the invention as a mild detergent or aftertreatment agent, for example as a fabric softener before, they can in a preferred embodiment Cellulase, preferably in an amount of 0.005 to 2 wt .-%, especially preferably from 0.01 to 1% by weight, in particular from 0.02 to 0.5% by weight, in each case based on the total agent included.

In a preferred embodiment are the inventive Textile care products in liquid form and advantageously point a viscosity of 50 to 5000 m · Pas especially preferably from 50 to 3000 m · Pas and in particular from 500 to 1500 m · Pas (measured at 20 ° C with a rotational viscometer (Brookfield RV, spindle 2) at 20 rpm (rpm: revolutions per minute)) on.

preferred Liquid fabric care products contain in a preferred Embodiment one or more non-aqueous, water-miscible solvents.

Solvent, in the water-containing agents according to the invention can be used, for example, come from the Group of mono- or polyhydric alcohols, alkanolamines or glycol ethers, if they are in the concentration range desired for use are miscible with water. Preferably, the solvents selected from ethanol, n- or i-propanol, butanols, Glycol, propane or butanediol, glycerol, diglycol, propyl or Butyl diglycol, hexylene glycol, ethylene glycol methyl ether, ethylene glycol ethyl ether, Ethylene glycol propyl ether, ethylene glycol mono-n-butyl ether, diethylene glycol methyl ether, Diethylene glycol ethyl ether, propylene glycol methyl, ethyl or propyl ether, Butoxy-propoxy-propanol (BPP), dipropylene glycol monomethyl, or ethyl ether, di-isopropylene glycol monomethyl, or ethyl ether, Methoxy, ethoxy or butoxytriglycol, 1-butoxyethoxy-2-propanol, 3-methyl-3-methoxybutanol, propylene glycol t-butyl ether and mixtures this solvent.

Some glycol ethers are available under the trade name Arcosolv ^® (Arco Chemical Co.) or Cellosolve, carbitol ^® or Propasol ^® (Union Carbide Corp.); this includes z. B. ButylCarbitol® ^{®, ®} hexyl carbitol, methyl ^®, and Carbitol ^® itself, (2- (2-ethoxy) ethoxy) ethanol. The choice of glycol ether can be readily made by one skilled in the art on the basis of its volatility, water solubility, weight percent of the total agent, and the like. Pyrrolidone solvents, such as N-alkylpyrrolidones, for example Example, N-methyl-2-pyrrolidone or NC ₈ -C ₁₂ alkylpyrrolidone, or 2-pyrrolidone, can also be used. Further preferably, alcohols can be used. These include low molecular weight liquid polyethylene glycols, for example polyethylene glycols having a molecular weight of 200, 300, 400 or 600. Further suitable other alcohols are, for example, lower alcohols such as ethanol, propanol, isopropanol and n-butanol, C ₂ -C ₄ - Polyols, such as diols or triols, for example ethylene glycol, propylene glycol, glycerol or mixtures thereof.

The Contain textile-cleaning agents according to the invention, if they are in liquid form, in a preferred Embodiment up to 95 wt .-%, particularly preferably 20 to 90 wt .-% and in particular 50 to 80 wt .-% of one or more Solvent, preferably water-soluble solvents and especially water.

In an embodiment of the invention contain the fabric care agents additional plasticizer components, preferably cationic surfactants. Especially when washing sensitive textiles, such as Silk, wool or linen that washed at low temperatures and ironed, is the use of additional Plasticizer components possible. In addition to the invention to be used Active ingredients may include such conventional plasticizer components additionally facilitate the ironing of textiles and to further reduce the static charge of the textile materials contribute.

Examples for fabric softening components are quaternary Ammonium compounds, cationic polymers and emulsifiers, such as they are used in hair care products and also in means for Textilavivage.

wobei in (IV) R und R¹ für einen acyclischen Alkylrest mit 12 bis 24 Kohlenstoffatomen, R² für einen gesättigten C₁-C₄ Alkyl- oder Hydroxyalkylrest steht, R³ entweder gleich R, R¹ oder R² ist oder für einen aromatischen Rest steht. X^– steht entweder für ein Halogenid-, Methosulfat-, Methophosphat- oder Phosphation sowie Mischungen aus diesen. Beispiele für kationische Verbindungen der Formel (IV) sind Didecyldimethylammoniumchlorid, Ditalgdimethylammoniumchlorid oder Dihexadecylammoniumchlorid.Suitable examples are quaternary ammonium compounds of the formulas (IV) and (V),

wherein in (IV) R and R ^{1 is} an acyclic alkyl radical having 12 to 24 carbon atoms, R ^{2 is} a saturated C ₁ -C ₄ alkyl or hydroxyalkyl radical, R ^{3 is} either R, R ¹ or R ² or is a aromatic residue stands. X ^- is either a halide, methosulfate, methophosphate or phosphate ion and mixtures thereof. Examples of cationic compounds of the formula (IV) are didecyldimethylammonium chloride, ditallowdimethylammonium chloride or dihexadecylammonium chloride.

Compounds of formula (V) are so-called ester quats. Esterquats are characterized by their good biodegradability and are preferred in the context of the present invention. Here, R ^{4 is} an aliphatic alkyl radical having 12 to 22 carbon atoms with 0, 1, 2 or 3 double bonds; R ⁵ is H, OH or O (CO) R ⁷ , R ⁶ is independently of R ^{5 is} H, OH or O (CO) R ⁸ , wherein R ⁷ and R ⁸ are each independently an aliphatic alkyl radical having 12 to 22 carbon atoms with 0, 1, 2 or 3 double bonds. m, n and p can each independently be 1, 2 or 3. X ^- may be either a halide, methosulfate, methophosphate or phosphate ion, as well as mixtures of these. Preference is given to compounds which contain the group O (CO) R ⁷ for R ⁵ and to alkyl radicals having 16 to 18 carbon atoms for R ⁴ and R ⁷ . Particularly preferred are compounds in which R ^{6 is} also OH. Examples of compounds of the formula (V) are methyl N- (2-hydroxyethyl) -N, N-di (tallowacyl-oxyethyl) ammonium methosulfate, bis (palmitoyl) -ethylhydroxyethyl-methyl-ammonium methosulfate or methyl-N , N-bis (acyloxyethyl) -N- (2-hydroxyethyl) ammonium methosulfate. If quaternized compounds of the formula (V) are used which have unsaturated alkyl chains, the acyl groups whose corresponding fatty acids have an iodine number between 5 and 80, preferably between 10 and 60 and in particular between 15 and 45 and which have a cis / trans isomer ratio are preferred (in wt .-%) of greater than 30:70, preferably greater than 50:50 and in particular greater than 70:30 have. Commercial examples are sold by Stepan under the tradename Stepantex ^® methylhydroxyalkyldialkoyloxyalkylammonium or those known under Dehyquart ^® Cognis products known under or Rewoquat ^® manufactured by Goldschmidt-Witco. Further preferred compounds are the diesterquats corresponding to formula (V ') which are obtainable under the name Rewoquat ^® 3099 W 222 LM or CR, and in addition to the softness also additionally provide stability and color protection.

R ²¹ and R ²² are each independently an aliphatic radical having 12 to 22 carbon atoms with 0, 1, 2 or 3 double bonds.

wobei R⁹ für H oder einen gesättigten Alkylrest mit 1 bis 4 Kohlenstoffatomen, R¹⁰ und R¹¹ unabhängig voneinander jeweils für einen aliphatischen, gesättigten oder ungesättigten Alkylrest mit 12 bis 18 Kohlenstoffatomen, R¹⁰ alternativ auch für O(CO)R²⁰ stehen kann, wobei R²⁰ einen aliphatischen, gesättigten oder ungesättigten Alkylrest mit 12 bis 18 Kohlenstoffatomen bedeutet, und Z eine NH-Gruppe oder Sauerstoffbedeutet und X^– ein Anion ist. q kann ganzzahlige Werte zwischen 1 und 4 annehmen.In addition to the quaternary compounds described above, it is also possible to use other known compounds, for example quaternary imidazolinium compounds of the formula (VI)

where R ^{9 is} H or a saturated alkyl radical having 1 to 4 carbon atoms, R ¹⁰ and R ¹¹ are each independently an aliphatic, saturated or unsaturated alkyl radical having 12 to 18 carbon atoms, R ^{10 may} alternatively be O (CO) R ²⁰ wherein R ^{20 is} an aliphatic, saturated or unsaturated alkyl radical having 12 to 18 carbon atoms, and Z is an NH group or oxygen and X ^{- is} an anion. q can take integer values between 1 and 4.

wobei R¹², R¹³ und R¹⁴ unabhängig voneinander für eine C_1-4-Alkyl-, Alkenyl- oder Hydroxyalkylgruppe steht, R¹⁵ und R¹⁶ jeweils unabhängig ausgewählt eine C_8-28-Alkylgruppe darstellt und r eine Zahl zwischen 0 und 5 ist.Further suitable quaternary compounds are described by formula (VII)

wherein R ¹² , R ¹³ and R ¹⁴ independently represent a C _1-4 alkyl, alkenyl or hydroxyalkyl group, each of R ¹⁵ and R ¹⁶ independently represents a C _8-28 alkyl group and r is a number between 0 and 5 is.

Next said compounds of formulas (IV) to (VII) can also short-chain, water-soluble, quaternary ammonium compounds be used, such as trihydroxyethylmethylammonium methosulfate or the alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkylmethylammonium chlorides, e.g. Cetyltrimethylammonium chloride, Stearyltrimethylammonium chloride, distearyldimethylammonium chloride, Lauryldimethylammonium chloride, Lauryldimethylbenzylammoniumchlorid and tricetylmethylammonium chloride.

Also protonated alkylamine compounds which have a softening effect, and the non-quaternized, protonated precursors of cationic Emulsifiers are suitable.

Further Cationic compounds which can be used according to the invention represent the quaternized protein hydrolysates.

Suitable cationic polymers include the polyquaternium polymers as described in the CTFA Cosmetic Ingredient Dictionary (The Cosmetic, Toiletry and Fragrance, Inc., 1997), in particular the Polyquaternium-6, Polyquaternium-7, Polyquaternium, also known as Merquats. 10 polymers (Ucare Polymer IR 400; Amerchol), polyquaternium-4 copolymers such as graft copolymers having a cellulose backbone and quaternary ammonium groups bonded via allyldimethylammonium chloride, cationic cellulose derivatives such as cationic guar such as guar hydroxypropyltriammonium chloride, and similar quaternized guar gum. Derivatives (eg Cosmedia Guar, manufacturer: Cognis GmbH), cationic quaternary sugar derivatives (cationic alkyl polyglucosides), eg. , The commercial product Glucquat ^® 100, according to CTFA nomenclature a "lauryl methyl Gluceth 10 Hydroxypropyl Dimonium Chloride", copolymers of PVP and dimethylaminomethacrylate, copolymers of vinylimidazole and vinylpyrrolidone, aminosilicone polymers and copolymers.

Polyquaternized polymers (for example, Luviquat Care by BASF.), And cationic biopolymers based on chitin and derivatives thereof, for example, under the trade designation chitosan ^® (manufacturer: Cognis) polymer obtainable.

Also suitable are cationic silicone oils such as the commercially available products Q2-7224 (manufacturer: Dow Corning, a stabilized trimethylsilylamodimethicone), Dow Corning 929 emulsion (containing a hydroxylamino-modified silicone, also referred to as amodimethicone), SM-2059 (manufacturer: General Electric), SLM-55067 ( manufacturer: Wacker) Abil ^® -Quat 3270 and 3272 (manufacturer: Goldschmidt-Rewo; diquaternary polydimethylsiloxanes, quaternium-80), and Silicone quat Rewoquat ^® SQ 1 (Tegopren ^® 6922, manufacturer: Goldschmidt-Rewo).

die Alkylamidoamine in ihrer nicht quaternierten oder, wie dargestellt, ihrer quaternierten Form, sein können. R¹⁷ kann ein aliphatischer Alkylrest mit 12 bis 22 Kohlenstoffatomen mit 0, 1, 2 oder 3 Doppelbindungen sein. s kann Werte zwischen 0 und 5 annehmen. R¹⁸ und R¹⁹ stehen unabhängig voneinander jeweils für H, C_1-4-Alkyl oder Hydroxyalkyl. Bevorzugte Verbindungen sind Fettsäureamidoamine wie das unter der Bezeichnung Tego Amid^®S 18 erhältliche Stearylamidopropyldimethylamin oder das unter der Bezeichnung Stepantex^® X 9124 erhältliche 3-Talgamidopropyl-trimethylammonium-methosulfat, die sich neben einer guten konditionierenden Wirkung auch durch farbübertragungsinhibierende Wirkung sowie speziell durch ihre gute biologische Abbaubarkeit auszeichnen. Besonders bevorzugt sind alkylierte quaternäre Ammoniumverbindungen, von denen mindestens eine Alkylkette durch eine Estergruppe und/oder Amidogruppe unterbrochen ist, insbesondere N-Methyl-N(2-hydroxyethyl)-N,N-(ditalgacyloxyethyl)ammoniummethosulfat und/oder N-Methyl-N(2-hydroxyethyl)-N,N-(palmitoyloxyethyl)ammoniummethosulfat.It is likewise possible to use compounds of the formula (VIII)

the alkylamidoamines may be in their quaternized or, as shown, their quaternized form. R ¹⁷ may be an aliphatic alkyl radical having 12 to 22 carbon atoms with 0, 1, 2 or 3 double bonds. s can take values between 0 and 5. R ¹⁸ and R ¹⁹ are each independently H, C _1-4 alkyl or hydroxyalkyl. Preferred compounds are fatty acid amidoamines such as Stearylamidopropyldimethylamin available under the name Tego Amid ^® S 18 or 3-Talgamidopropyl-trimethylammonium methosulfate available under the name Stepantex ^® X 9124, which in addition to a good conditioning effect by color transfer inhibiting effect and especially by their good distinguish biodegradability. Particularly preferred are alkylated quaternary ammonium compounds of which at least one alkyl chain is interrupted by an ester group and / or amido group, in particular N-methyl-N (2-hydroxyethyl) -N, N- (ditalgacyloxyethyl) ammonium methosulfate and / or N-methyl-N (2-hydroxyethyl) -N, N- (palmitoyloxyethyl) methosulfate.

When nonionic plasticizers are mainly polyoxyalkylene glycol alkanoates, Polybutylenes, ethoxylated fatty acid ethanolamides, alkylpolyglycosides and sorbitan mono-, di- and triesters.

In a preferred embodiment contain inventive Mild detergent cationic surfactants, preferably alkylated quaternary Ammonium compounds, of which at least one alkyl chain by a Ester group and / or amido group is interrupted, in particular N-methyl-N (2-hydroxyethyl) -N, N- (ditalgacyloxyethyl) methosulfate or N-methyl-N (2-hydroxyethyl) -N, N- (dipalmitoylethyl) ammonium methosulfate.

In a further preferred embodiment include the Fabric care products according to the invention plasticizer components in an amount up to 35% by weight, preferably from 0.1 to 25% by weight, particularly preferably from 0.5 to 15% by weight and in particular from 1 to 10 wt .-%, each based on the total agent.

In a particularly preferred embodiment of the invention are the textile care agents according to the invention as a mild detergent or fabric softener, containing Plasticizers, preferably cationic plasticizers, more preferred Esterquats.

additionally to the aforementioned components, the inventive Textile care products contain pearlescent agents. Impart pearlescing agent the textiles an extra shine and therefore preferably in fine detergents according to the invention used.

When Pearlescing agents are, for example, suitable: alkylene glycol esters; fatty acid; partial glycerides; Esters of polyvalent, optionally hydroxysubstituted carboxylic acids with fatty alcohols with 6 to 22 carbon atoms; Fatty substances, such as fatty alcohols, Fatty ketones, fatty aldehydes, fatty ethers and fatty carbonates, in total have at least 24 carbon atoms; Ring opening products of Olefin epoxides having 12 to 22 carbon atoms with fatty alcohols with 12 to 22 carbon atoms, fatty acids and / or polyols having 2 to 15 carbon atoms and 2 to 10 hydroxyl groups as well their mixtures.

Furthermore, liquid textile care agents according to the invention may additionally contain thickeners. The use of thickeners in the textile care agents according to the invention which are to find use as liquid detergents has proven particularly advantageous. To increase consumer acceptance, the use of thickening agents has proven particularly useful in gel-type liquid detergents. The thickened consistency of the agent simplifies the application of the agent directly to the spots to be treated. A bleeding, as usual with thin liquids, this is prevented.

Out naturally derived polymers used as thickening agents For example, agar-agar, carrageenan, Tragacanth, gum arabic, alginates, pectins, polyoses, guar flour, Locust bean gum, starch, dextrins, gelatin and Casein.

modified Natural products come mainly from the group of modified starches and celluloses exemplified by carboxymethylcellulose and nonionic Cellulose ethers such as hydroxyethyl and propyl cellulose and gum ethers called.

A large group of thickeners, the most widely used find in the most diverse fields of application, are the fully synthetic Polymers such as polyacrylic and polymethacrylic compounds, vinyl polymers, Polycarboxylic acids, polyethers, polyimines, polyamides and polyurethanes.

Thickening agents from the substance classes mentioned are commercially available and, for example, under the trade names Acusol ^® -820 (methacrylic acid (stearyl alcohol 20 EO) ester-acrylic acid copolymer, 30% in water, Rohm & Haas), Dapral ^® -GT- 282-S (alkyl polyglycol ethers, Akzo), DEUTEROL ^® polymer-11 (dicarboxylic acid copolymer, Schoner GmbH) deuteron ^® -xg (anionic heteropolysaccharide based on β-D-glucose, D-mannose, D-glucuronic acid, Schoner GmbH ) deuteron ^® -XN (nonionic polysaccharide Schoner GmbH), DICRYLAN ^® -Verdicker-O (ethylene oxide adduct, 50% solution in water / isopropanol, Pfersse Chemie), EMA ^® -81 and EMA®-91 (ethylene-maleic anhydride copolymer, Monsanto), thickener QR-1001 (polyurethane emulsion, 19 to 21% strength in water / diglyme, Rohm & Haas), Mirox ^® -AM (anionic acrylic acid-acrylate copolymer dispersion, 25% in water , Stockhausen), SER-AD FX 1100 (hydrophobic urethane polymer, servo Delden), Shellflo ^® -S (hochmolekul ares polysaccharide, stabilized with formaldehyde, Shell), and Shellflo XA ^® (xanthan biopolymer, stabilized with formaldehyde, Shell).

One preferably to be used polymeric polysaccharide thickener is xanthan, a microbial anionic heteropolysaccharide that of Xanthomonas campestris and some other species under aerobic Conditions is produced and a molecular weight of 2 to 15 million g / mole. Xanthan is made from a chain bound with β-1,4 Glucose (cellulose) with side chains formed. The structure of Subgroups consists of glucose, mannose, glucuronic acid, Acetate and pyruvate, where the number of pyruvate units is the viscosity of xanthan gum.

With particular advantage can be due to their very extensive Stability Use xanthans and modified xanthans.

In a preferred embodiment, the inventive Fabric care thickener, preferably in amounts of up to 10 wt .-%, particularly preferably up to 5 wt .-%, in particular of 0.1 to 1 wt .-%, each based on the total agent.

Farther can the textile care agents of the invention additionally odor absorbers and / or color transfer inhibitors contain. In particular for the inventive Textile care products as fine. Aftertreatment and liquid detergents present, the use of Farbübertragungsinhibtoren proven. For the deodorization of evil-smelling Recipe ingredients, such as amine-containing components, but also for sustainable deodorization of the washed textiles The use of odor absorbers has proved very helpful.

In a preferred embodiment, the fabric care agents according to the invention optionally contain 0.1 wt .-% to 2 wt .-%, preferably 0.2 wt .-% to 1 wt .-% dye transfer inhibitor, which in a preferred embodiment of the invention, a polymer of vinylpyrrolidone , Vinylimidazole, vinylpyridine N-oxide or a copolymer of these. Useful are, for example, polyvinylpyrrolidones having molecular weights of from 15,000 to 50,000 as well as polyvinylpyrrolidones having molecular weights above 1,000,000, in particular from 1,500,000 to 4,000,000, N-vinylimidazole / N-vinylpyrrolidone copolymers, polyvinyl oxazolidones, copolymers based on vinyl monomers and carboxylic acid amides, pyrrolidone group-containing polyesters and polyamides, grafted polyamidoamines and polyethyleneimines, 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 produces 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 in this case be It is also possible to additionally use the abovementioned polymeric color transfer inhibiting agents. 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.

preferred Deodorizing substances in the sense of the invention are one or more Metal salts of an unbranched or branched, unsaturated or saturated, mono- or polyhydroxylated fatty acid having at least 16 carbon atoms and / or a rosin acid with the exception of the alkali metal salts and any mixtures thereof. A particularly preferred unbranched or branched, unsaturated or saturated, mono- or polyhydroxylated fatty acid with at least 16 carbon atoms is ricinoleic acid. A particularly preferred rosin acid is abietic acid. Preferred metals are the transition metals and the lanthanides, in particular the transition metals of groups VIIIa, Ib and IIb of the periodic table as well as lanthanum, cerium and neodymium, especially preferably cobalt, nickel, copper and zinc, extremely preferably zinc. The cobalt, nickel and copper salts and the zinc salts are similarly effective, for toxicological reasons However, the zinc salts are to be preferred. As advantageous and therefore particularly preferred to be used as deodorizing substances one or more metal salts of ricinoleic acid and / or abietic acid, preferably zinc ricinoleate and / or Zinc abietate, in particular zinc ricinoleate. As another suitable Deodorizing substances also prove to be within the meaning of the invention Cyclodextrins, and mixtures of the aforementioned metal salts with Cyclodextrin, preferably in a weight ratio of 1:10 to 10: 1, more preferably from 1: 5 to 5: 1 and especially from 1: 3 to 3: 1. The term "Cylcodextrin" includes all known cyclodextrins, d. H. both unsubstituted cyclodextrins with 6 to 12 glucose units, especially alpha, beta and gamma cyclodextrins as well as their mixtures and / or their derivatives and / or their Mixtures.

The Fabric care agents according to the invention can additionally other surfactants, for example amphoteric surfactants, contain.

To the amphoteric surfactants (zwitterionic surfactants) used according to the invention include betaines, amine oxides, alkylamidoalkylamines, alkyl-substituted amino acids, acylated amino acids or Biosurfactants, of which the betaines are within the scope of the invention Teaching are particularly preferred.

Suitable betaines are the alkylbetaines, the alkylamidobetaines, the imidazolinium betaines, the sulfobetaines (INCI Sultaines) and the phosphobetaines and preferably satisfy the formula IX, R ¹ - [CO-X- (CH ₂ ) _n ] _x -N ⁺ (R ² ) (R ³ ) - (CH ₂ ) _m - [CH (OH) -CH ₂ ] _y -Y (IX) in the R ^{1 is} a saturated or unsaturated C _6-22 alkyl radical, preferably C _8-18 alkyl, in particular a saturated C _10-16 alkyl radical, for example a saturated C _12-14 alkyl radical, X is NH, NR ⁴ with the C ₁₄ alkyl radical R ⁴ , O or S, n is a number from 1 to 10, preferably 2 to 5, in particular 3, x 0 or 1, preferably 1, R ² , R ^{3 are} independently of one another a C _1-4 -alkyl radical, optionally hydroxy-substituted such. A hydroxyethyl radical, but especially a methyl radical, m is a number from 1 to 4, in particular 1, 2 or 3, y is 0 or 1 and Y is COO, SO ₃ , OPO (OR ⁵ ) O or P (O) (OR ⁵ ) O, wherein R ^{5 is} a hydrogen atom or a C ₁₄ alkyl radical.

Preferred amphoteric surfactants are the alkylbetaines of the formula (IXa), the alkylamidobetaines of the formula (IXb), the sulfobetaines of the formula (IXc) and the amidosulfobetaines of the formula (IXd) R ¹ -N ⁺ (CH ₃ ) ₂ -CH ₂ COO ^- (IXa) R ¹ -CO-NH- (CH ₂ ) ₃ -N ⁺ (CH ₃ ) ₂ -CH ₂ COO ^- (IXb) R ^{1 is} -N ⁺ (CH ₃ ) ₂ -CH ₂ CH (OH) CH ₂ SO ₃ (IXc) R ¹ -CO-NH- (CH ₂ ) ₃ -N ⁺ (CH ₃ ) ₂ -CH ₂ CH (OH) CH ₂ SO ₃ (IXd) in which R ^{1 has} the same meaning as in formula IX.

Particularly preferred amphoteric surfactants are the carbobetaines, in particular the carbo-betaines of For mel (IXa) and (IXb), most preferably the alkylamido betaines of the formula (IXb).

Examples suitable betaines and sulfobetaines are the following according to INCI named compounds: Almondamidopropyl Betaine, Apricotamidopropyl Betaine, Avocadamidopropyl Betaine, Babassuamidopropyl Betaine, Behenamidopropyl Betaine, Behenyl Betaine, Betaine, Canolamidopropyl Betaines, caprylic / capramidopropyl betaines, carnitines, cetyl betaines, Cocamidoethyl Betaine, Cocamidopropyl Betaine, Cocamidopropyl Hydroxysultaine, Coco-Betaine, Coco-Hydroxysultaine, Coco / Oleamidopropyl Betaine, Coco-sultaine, decyl betaine, dihydroxyethyl oleyl glycinate, dihydroxyethyl Soy glycinate, dihydroxyethyl stearyl glycinate, dihydroxyethyl Tallow Glycinate, Dimethicone Propyl PG-Betaine, Erucamidopropyl Hydroxysultaine, Hydrogenated Tallow Betaine, Isostearamidopropyl Betaine, Lauramidopropyl Betaine, Lauryl Betaine, Lauryl Hydroxysultaine, Lauryl Sultaine, Milkamidopropyl Betaine, Minkamidopropyl Betaine, Myristamidopropyl betaine, myristyl betaine, oleamidopropyl betaine, Oleamidopropyl Hydroxysultaine, Oleyl Betaine, Olivamidopropyl Betaine, Palmamidopropyl Betaine, Palmitamidopropyl Betaine, Palmitoyl Carnitine, Palm Kernelamidopropyl Betaine, Polytetrafluoroethylene Acetoxypropyl Betaine, Ricinoleamidopropyl Betaine, Sesamidopropyl Betaine, Soyamidopropyl Betaines, stearamidopropyl betaines, stearyl betaines, tallow amidopropyl Betaine, Tallowamidopropyl Hydroxysultaine, Tallow Betaine, Tallow Dihydroxyethyl betaines, undecylenamidopropyl betaines and wheat germamidopropyl Betaine.

The amine oxides suitable in accordance with the invention include alkylamine oxides, in particular alkyldimethylamine oxides, alkylamidoamine oxides and alkoxyalkylamine oxides. Preferred amine oxides satisfy formula XI or XII, R ⁶ R ⁷ R ⁸ N ⁺ -O ^- (XI) R ⁶ - [CO-NH- (CH ₂ ) _w ] _z -N ⁺ (R ⁷ ) (R ⁸ ) -O- (XII) in which R ⁶ is a saturated or unsaturated C _6-22 alkyl, preferably C _8-18 alkyl group, preferably a saturated C _10-16 alkyl group, for example a saturated C _12-14 alkyl group, in the alkylamidoamine oxides over a carbonylamidoalkylene -CO-NH- (CH ₂ ) _z and in the alkoxyalkylamine oxides via an oxaalkylene group -O- (CH ₂ ) - is bonded to the nitrogen atom N, wherein z is in each case a number from 1 to 10, preferably 2 to 5, in particular 3 is, and R ⁷ and R ^{8 are} independently a C _1-4 alkyl radical, optionally hydroxy-substituted, such as. B. is a hydroxyethyl radical, in particular a methyl radical.

Examples suitable amine oxides are the following according to INCI named compounds: Almondamidopropylamine Oxide, Babassuamidopropylamine Oxides, Behenamine Oxide, Cocamidopropyl Amine Oxide, Cocamidopropylamine Oxide, Cocamine Oxide, Coco-Morpholine Oxide, Decylamine Oxide, Decyltetradecylamines oxides, diaminopyrimidines oxides, dihydroxyethyl C8-10 alkoxypropylamines oxides, dihydroxyethyl C9-11 alkoxypropylamines Oxides, dihydroxyethyl C12-15 alkoxypropylamines oxides, dihydroxyethyl Cocamine oxides, dihydroxyethyl lauramine oxides, dihydroxyethyl stearamines Oxides, Dihydroxyethyl Tallowamine Oxide, Hydrogenated Palm Kernel Amine Oxide, Hydrogenated Tallowamine Oxide, Hydroxyethyl Hydroxypropyl C12-15 Alkoxypropylamines oxides, isostearamidopropylamines oxides, isostearamidopropyl Morpholine oxides, Lauramidopropylamine oxides, Lauramine oxides, methyl Morpholine Oxide, Milkamidopropyl Amine Oxide, Minkamidopropylamine Oxides, myristamidopropylamine oxides, myristamine oxides, myristyl / cetyl Amine oxides, Oleamidopropylamine oxides, Oleamine oxides, Olivamidopropylamine Oxides, palmitamidopropylamine oxides, palmitamine oxides, PEG-3 lauramines Oxides, Potassium Dihydroxyethyl Cocamine Oxides Phosphate, Potassium Trisphosphonomethylamine oxides, sesamidopropylamine oxides, soyamidopropylamines Oxides, stearamidopropylamines oxides, stearamines oxides, tallow amidopropyl amines Oxides, tallowamine oxides, undecylenamidopropylamine oxides and wheat Germamidopropylamine oxides.

The alkylamidoalkylamines (INCI alkylamido alkylamines) are amphoteric surfactants of the formula (XIII) R ⁹ CO-NR ¹⁰ - (CH ₂ ) _i -N (R ¹¹ ) - (CH ₂ CH ₂ O) _j - (CH ₂ ) _k - [CH (OH)] ₁ -CH ₂ -Z-OM (XIII ) in which R ⁹ is a saturated or unsaturated C _6-22 alkyl, preferably C _8-18 alkyl group, preferably a saturated C _10-16 alkyl group, for example a saturated C _12-14 alkyl group, R ¹⁰ is hydrogen or a C ₁₄ -Alkyl, preferably H, i is a number from 1 to 10, preferably 2 to 5, in particular 2 or 3, R ^{11 is} hydrogen or CH ₂ COOM, j is a number from 1 to 4, preferably 1 or 2, in particular 1, k Number is from 0 to 4, preferably 0 or 1.1, 0 or 1, where k = 1, when 1 = 1, Z is CO, SO ₂ , OPO (OR ¹² ) or P (O) (OR ¹² ), wherein R ^{12 is} a C _1-4 alkyl radical or M, and M is hydrogen, an alkali metal, an alkaline earth metal or a protonated alkanolamine, e.g. B. protonated mono-, di- or triethanolamine, is.

Preferred representatives satisfy the formulas XIIIa to XIIId, R ⁹ -CO-NH- (CH ₂ ) ₂ -N (R ¹¹ ) -CH ₂ CH ₂ O-CH ₂ -COOM (XIIIa) R ⁹ -CO-NH- (CH ₂ ) ₂ -N (R ¹¹ ) -CH ₂ CH ₂ O-CH ₂ CH ₂ -COOM (XIIIb) R ⁹ -CO-NH- (CH ₂ ) ₂ -N (R ¹¹ ) -CH ₂ CH ₂ O-CH ₂ CH (OH) CH ₂ -SO ₃ M (XIIIc) R ⁹ -CO-NH- (CH ₂ ) ₂ N (R ¹¹ ) -CH ₂ CH ₂ O-CH ₂ CH (OH) CH ₂ -OPO ₃ HM (XIIId) in which R ⁹ , R ¹¹ and M have the same meaning as in formula (XIII). Exemplary alkylamidoalkylamines are the following named according to INCI compounds: Cocoamphodipropionic Acid, Cocobetainamido amphopropionates, DEA-Cocoamphodipropionate, Disodium Caproamphodiacetate, Disodium Caproamphodipropionate, Disodium Capryloamphodiacetate, Disodium Capryloamphodipropionate, Disodium Cocoamphocarboxyethylhydroxypropylsulfonate, Disodium Cocoamphodiacetate, Disodium Cocoamphodipropionate, Disodium Isostearoamphodiacetate, Disodium Isostearoamphodipropionate, Disodium laureth 5 Carboxyamphodiacetate, Disodium Lauroamphodiacetate, Disodium Lauroamphodipropionate, Disodium Oleoamphodipropionate, Disodium PPG-2-Isodeceth-7 Carboxyamphodiacetate, Disodium Stearoamphodiacetate, Disodium Tallowamphodiacetate, Disodium Wheatgermamphodiacetate, Lauroamphodipropionic Acid, Quaternium-85, Sodium Caproamphoacetate, Sodium Caproamphohydroxypropylsulfonate, Sodium Caproamphopropionate, Sodium Capryloamphoacetate, Sodium Capryloamphohydroxypropylsulfonate, Sodium Capryl oamphopropionate, Sodium Cocoamphoacetate, Sodium Cocoamphohydroxypropylsulfonate, Sodium Cocoamphopropionate, Sodium Cornamphopropionate, Sodium Isostearoamphoacetate, Sodium Isostearoamphopropionate, Sodium lauroamphoacetate, sodium Lauroamphohydroxypropylsulfonate, Sodium Lauroampho PG-Acetate Phosphate, Sodium Lauroamphopropionate, Sodium Myristoamphoacetate, Sodium Oleoamphoacetate, Sodium Oleoamphohydroxypropylsulfonate, Sodium Oleoamphopropionate, Sodium Ricinoleoamphoacetate , Sodium Stearoamphoacetate, Sodium Stearoamphohydroxypropylsulfonate, Sodium Stearoamphopropionate, Sodium Tallamphopropionate, Sodium Tallowamphoacetate, Sodium Undecylenoamphoacetate, Sodium Undecylenoamphopropionate, Sodium Wheat Germamphoacetate, and Trisodium Lauroampho PG-Acetate Chloride Phosphate.

Alkyl-substituted amino acids (INCI alkyl-substituted amino acids) which are preferred according to the invention are monoalkyl-substituted amino acids of the formula (XIV) R ¹³ -NH-CH (R ¹⁴ ) - (CH ₂ ) _u -COOM '(XIV) in which R ¹³ is a saturated or unsaturated C _6-22 alkyl, preferably C _8-18 alkyl group, preferably a saturated C _10-16 alkyl group, for example a saturated C _12-14 alkyl group, R ¹⁴ is hydrogen or a C _{1- 4} alkyl, preferably H, u is a number from 0 to 4, preferably 0 or 1, in particular 1, and M 'is hydrogen, an alkali metal, an alkaline earth metal or a protonated alkanolamine, for. B. protonated mono-, di- or triethanolamine, is alkyl-substituted imino acids according to formula (XV), R ¹⁵ -N - [(CH ₂ ) - COOM ''] ₂ (XV) wherein R is a saturated or unsaturated C _6-22 alkyl group ^15, preferably C _8-18 alkyl group, preferably a saturated C _10-16 alkyl group, for example a saturated C _12-14 alkyl group, v is a number 1 to 5 , preferably 2 or 3, in particular 2, and M "is hydrogen, an alkali metal, an alkaline earth metal or a protonated alkanolamine, for example protonated mono-, di- or triethanolamine, where M" in the two carboxy groups have the same or different meanings can have, for. B. hydrogen and sodium or twice sodium, and mono- or dialkyl-substituted natural amino acids according to formula (XVI), R ¹⁶ -N (R ¹⁷ ) -CH (R ¹⁸ ) -COOM '''(XVI) in the R ^{16 is} a saturated or unsaturated C _6-22 alkyl radical, preferably C _8-18 alkyl, in particular a saturated C _10-16 alkyl radical, for example a saturated C _12-14 alkyl radical, R ^{17 is} hydrogen or a C _{1 -4} alkyl, optionally hydroxy or amine substituted, for. A methyl, ethyl, hydroxyethyl or aminopropyl radical, R ^{18 is} the radical of one of the 20 natural α-amino acids H ₂ NCH (R ¹⁸ ) COOH, and M '''is hydrogen, an alkali metal, an alkaline earth metal or a protonated alkanolamine , z. B. protonated mono-, di- or triethanolamine, is.

Particularly preferred alkyl-substituted amino acids are the Aminopropionate according to formula (XI Va) R ¹³ -NH-CH ₂ CH ₂ COOM '(XIVa) in which R ¹³ and M 'have the same meaning as in formula (XIV).

exemplary Alkyl-substituted amino acids are the following according to INCI named compounds: aminopropyl laurylglutamine, cocaminobutyric Acid, cocaminopropionic acid, DEA-lauraminopropionate, disodium Cocaminopropyl iminodiacetate, disodium dicarboxyethyl cocopropylenediamine, Disodium Lauriminodipropionate, Disodium Steariminodipropionate, Disodium Tallowiminodipropionate, Lauraminopropionic Acid, Lauryl Aminopropylglycines, lauryl diethylenediaminoglycines, myristaminopropionic Acid, Sodium C12-15 Alkoxypropyl Iminodipropionate, Sodium Cocaminopropionate, Sodium Sodium Lauraminopropionate, Sodium Lauriminodipropionate, Sodium Lauroyl methylaminopropionate, TEA-lauraminopropionate and TEA-myristaminopropionate.

Acylated amino acids are amino acids, in particular the 20 natural α-amino acids which carry on the amino nitrogen the acyl radical R ¹⁹ CO of a saturated or unsaturated fatty acid R ¹⁹ COOH, where R ^{19 is} a saturated or unsaturated C _6-22 alkyl radical, preferably C _8-18 Alkyl, in particular a saturated C _10-16 alkyl radical, for example a saturated C _12-14 alkyl radical. The acylated amino acids may also be used as the alkali metal salt, alkaline earth metal salt or alkanolammonium salt, e.g. As mono-, di- or triethanolammonium, are used. Exemplary acylated amino acids are the acyl derivatives summarized under INCI under Acids, eg. Sodium Cocoyl Glutamate, Lauroyl Glutamic Acid, Capryloyl Glycine or Myristoyl Methylalanine.

In In a preferred embodiment, the total surfactant content is the textile care agent according to the invention, without the amount of fatty acid soap, below 55% by weight, preferably below 50% by weight, more preferably between 12 and 48 Wt .-%, each based on the total agent.

The Fabric care agents according to the invention can additionally contain other detergent additives, for example from the group of builders, bleaches, bleach activators, Electrolytes, pH adjusters, fragrances, perfume carriers, Fluorescent agents, dyes, foam inhibitors, grayness inhibitors, antimicrobial agents, germicides, fungicides, antioxidants, Antistatic agents, ironing aids, UV absorbers, optical brighteners, Anti redeposition agents, viscosity regulators, inlet preventer, Corrosion inhibitors, preservatives, repellents and impregnating agents.

The agents according to the invention can be builders contain. It can be all usually builders used in detergents and cleaners be introduced into the agent according to the invention, in particular zeolites, silicates, carbonates, organic cobuilders and - if so, no ecological prejudices against their use also consist of phosphates.

Suitable crystalline layered sodium silicates have the general formula NaMSi _x O _{2x + 1} · yH ₂ O, where M is sodium or hydrogen, x is a number from 1.9 to 4 and y is a number from 0 to 20 and preferred values for x 2 , 3 or 4 are. Preferred crystalline layered silicates of the formula given are those in which M is sodium and x assumes the values 2 or 3. In particular, both β- and δ-sodium disilicates Na ₂ Si ₂ O ₅ .yH ₂ O are preferred.

It is also possible to use amorphous sodium silicates with a Na ₂ O: SiO ₂ modulus of from 1: 2 to 1: 3.3, preferably from 1: 2 to 1: 2.8 and in particular from 1: 2 to 1: 2.6, which Delayed and have secondary washing properties. The dissolution delay compared with conventional amorphous sodium silicates may have been caused in various ways, for example by surface treatment, compounding, compaction / densification or by overdrying. In the context of this invention, the term "amorphous" is also understood to mean "X-ray amorphous". This means that the silicates do not yield sharp X-ray reflections typical of crystalline substances in X-ray diffraction experiments, but at most one or more maxima of the scattered X-rays having a width of several degrees of diffraction angle. However, it may very well even lead to particularly good Builderei properties when the silicate particles in electron diffraction experiments provide washed-out or even sharp diffraction maxima. This is to be interpreted as meaning that the products have microcrystalline regions of size 10 to a few hundred nm, values of up to max. 50 nm and in particular up to max. 20 nm are preferred. Such so-called X-ray amorphous silicates likewise have a dissolution delay compared with the conventional water glasses. Particularly preferred are compacted / compacted amor phe silicates, compounded amorphous silicates and overdried X-ray amorphous silicates.

The finely crystalline, synthetic and bound water-containing zeolite is preferably zeolite A and / or P. As zeolite P zeolite MAP ^® (commercial product from Crosfield) is particularly preferred. Also suitable, however, are zeolite X and mixtures of A, X and / or P. Commercially available and preferably usable in the context of the present invention is, for example, a cocrystal of zeolite X and zeolite A (about 80% by weight of zeolite X) ), produced by the company CONDEA Augusts S. p. A. sold under the brand name VEGOBOND AX ^® and by the formula nNa ₂ O · (1 - n) K ₂ O · Al ₂ O ₃ · (2 - 2.5) SiO ₂ · (3.5-5.5) H ₂ O can be described. Suitable zeolites have an average particle size of less than 10 μm (volume distribution, measuring method: Coulter Counter) and preferably contain 18 to 22% by weight, in particular 20 to 22% by weight, of bound water. The zeolites can also be used as overdried zeolites with lower water contents and then, due to their hygroscopicity, are suitable for removing unwanted residual traces of free water.

Of course it is also possible to use the generally known phosphates as builders, if such use is not for environmental reasons should be avoided. Particularly suitable are the sodium salts the orthophosphates, the pyrophosphates and in particular the tripolyphosphates.

When Builders are further suitable polymeric polycarboxylates, these are for example, the alkali metal salts of polyacrylic acid or polymethacrylic acid, for example those with a relative molecular weight of 500 to 70,000 g / mol.

The molecular weights stated here for polymeric polycarboxylates are weight-average molar masses M _{w of} the particular acid form which can in principle be determined by means of gel permeation chromatography (GPC), a UV detector being used. The measurement is carried out against an external standard, for example against a polyacrylic acid standard, which provides realistic molecular weight values due to its structural relationship with the polymers investigated. This information often differs significantly from the molecular weight data in which polystyrene sulfonic acids are used as standard. The molar masses measured against polystyrenesulfonic acids are generally much higher. Suitable polymers are in particular polyacrylates, which preferably have a molecular weight of from 2,000 to 20,000 g / mol. Because of their superior solubility, the short-chain polyacrylates, which have molecular weights of from 2,000 to 10,000 g / mol, and particularly preferably from 3,000 to 5,000 g / mol, may again be preferred from this group.

suitable Polymers may also include substances that partially or entirely from units of vinyl alcohol or its Derivatives exist.

Suitable are furthermore copolymeric polycarboxylates, especially those of Acrylic acid with methacrylic acid and acrylic acid or methacrylic acid with maleic acid. As special suitable copolymers of acrylic acid with maleic acid proven, the 50 to 90 wt .-% acrylic acid and 50 to 10 Wt .-% maleic acid. Your molecular weight, based on free acids, is generally 2,000 to 70,000 g / mol, preferably 20,000 to 50,000 g / mol and in particular 30,000 to 40,000 g / mol. The (co) polymeric polycarboxylates can be either as an aqueous solution or preferably used as a powder.

to Water solubility can improve the polymers also allylsulfonic acids, such as allyloxybenzenesulfonic acid and methallylsulfonic acid, as a monomer. Further preferred copolymers are those which are used as monomers acrolein and Acrylic acid / acrylic acid salts or acrolein and vinyl acetate.

As well as further preferred builder substances are polymeric aminodicarboxylic acids, to mention their salts or their precursors. Especially Preference is given to polyaspartic acids or their salts and Derivatives. Also suitable are polyvinylpyrrolidones, polyamine derivatives such as quaternized and / or ethoxylated hexamethylenediamines.

Further suitable builder substances are polyacetals which are prepared by reaction of dialdehydes with Polyolcarboxylic acids having 5 to 7C atoms and at least 3 hydroxyl groups can be obtained. Preferred polyacetals are obtained from dialdehydes such as glyoxal, glutaraldehyde, terephthalaldehyde and mixtures thereof and from polyol carboxylic acids such as gluconic acid and / or glucoheptonic acid.

Suitable as organic builders are also dextrins, that is, oligomers or polymers of carbohydrates, obtained by partial hydrolysis of starches can. The hydrolysis can be carried out according to customary, for example acid or enzyme catalyzed process can be performed. Preferably, they are hydrolysis products with middle Molar masses in the range of 400 to 500 000 g / mol. This is a polysaccharide with a dextrose equivalent (DE) in the range of 0.5 to 40, in particular from 2 to 30 preferred, DE being a common Measure of the reducing effect of a polysaccharide compared to dextrose, which has a DE of 100. Useful are both maltodextrins with a DE between 3 and 20 and dry glucose syrups with a DE between 20 and 37 as well as so-called yellow dextrins and white dextrins with higher molecular weights in the range from 2,000 to 30,000 g / mol. In the oxidized derivatives of such Dextrins are their reaction products with oxidizing agents, which are capable of at least one alcohol function of the saccharide ring, optionally with cleavage of the ring, to the carboxylic acid function to oxidize. A product oxidized at C6 of the saccharide ring can be particularly advantageous.

Also Oxydisuccinates and other derivatives of disuccinates, preferably Ethylenediamine disuccinate are other suitable cobuilders. there ethylenediamine-N, N'-disuccinate (EDDS) is preferably used in the form of its sodium or magnesium salts used. Further preferred are in this Also related glycerol disuccinates and glycerol trisuccinates. Suitable amounts are about 3 wt .-% to 15 wt .-%, based on the means.

The agents according to the invention may optionally Builders in amounts of 1 to 60 wt .-%, preferably Contain 20 to 50 wt .-%.

The agents of the invention may contain bleaching agents. Among the compounds serving as bleaches in water H ₂ O ₂ , sodium percarbonate, sodium perborate tetrahydrate and sodium perborate monohydrate are of particular importance. Other useful bleaching agents are, for example, peroxopyrophosphates, citrate perhydrates and persalts or peracids, such as persulfates or persulfuric acid. Also useful is the urea peroxohydrate percarbamide, which can be described by the formula H ₂ N-CO-NH ₂ .H ₂ O ₂ . Typical organic bleaches are the diacyl peroxides, such as dibenzoyl peroxide. Other typical organic bleaching agents are the peroxycarboxylic acids, examples of which include the alkyl peroxyacids and the aryl peroxyacids. Preferred representatives are the peroxybenzoic acid and its ring-substituted derivatives, such as alkylperoxybenzoic acids, but also peroxy-α-naphthoic acid and magnesium monoperphthalate, the aliphatic or substituted aliphatic peroxy acids, such as peroxylauric acid, peroxystearic acid, ε-phthalimidoperoxycaproic acid (Phthalimidoperoxyhexanoic acid, PAP), o-carboxybenzamidoperoxycaproic acid, N- Nonanoylamidoperadipic acid and N-nonanoylamidopersuccinates, and aliphatic and araliphatic peroxydicarboxylic acids such as 1,12-diperoxydodecanedicarboxylic acid, 1,9-diperoxyazelaic acid, diperoxysebacic acid, diperoxybrassic acid, the diperoxyphthalic acids, 2-decyldiperoxybutane-1,4-diacid, N, N-terephthaloyl-di ( 6-aminopercaproic acid) can be used. The agents according to the invention can particularly preferably contain phthalimidoperoxyhexanoic acid (PAP). If desired, the bleaching agents may be coated to protect against premature decomposition.

The agents of the invention may contain bleach activators. 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 tetraacetylglycoluril (TAGU), N- Acylimides, in particular N-nonanoylsuccinimide (NOSI), acylated phenolsulfonates, in particular n-nonanoylode or isononanoyloxybenzenesulfonate (n- or iso-NOBS), carboxylic anhydrides, in particular phthalic anhydride, acylated polyhydric alcohols, in particular triacetin, triethylacetylcitrate (TEAC), ethylene glycol diacetate, 2.5 -Diacetoxy-2,5-dihydrofuran and acetylated sorbitol and mannitol or mixtures thereof (SORMAN), acylated sugar derivatives, especially pentaacetylglucose (PAG), pentaacetylfruktose, tetraacetylxylose and octaacetyllactose 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. Another class of preferred bleach activators are the cationic acetonitrile derivatives RR'R''N ⁺ CH ₂ CN which give perimide acids under perhydrolysis conditions.

The agents according to the invention may contain electrolytes. As electrolytes from the group of inorganic salts, a wide number of different salts can be used. Preferred cations are the alkali and alkaline earth metals, preferred anions are the halides and sulfates. From a production point of view, the use of NaCl or MgCl ₂ in the agents according to the invention is preferred. The proportion of electrolytes in the inventive compositions is usually 0.5 to 5 wt .-%.

The agents according to the invention can pH adjusting agents contain. To the pH of the inventive The means to bring in the desired area, the Use of pH adjusters should be indicated. Can be used here All known acids or alkalis, provided their use is not from application or environmental Reasons or for reasons of consumer protection prohibits. Usually the amount exceeds this setting agent 2 wt .-% of the total formulation not.

The Agents according to the invention can and fragrances. Dyes and fragrances are the inventive Means added to the aesthetic impression of the products improve and the consumer in addition to the washing or cleaning performance a visual and sensory "typical and unmistakable" product to provide. As perfume oils or fragrances can be individual fragrance compounds, z. As the synthetic products of the ester, ether, aldehyde, Ketones, alcohols and hydrocarbons are used. fragrance compounds the type of ester are z. Benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, linalyl acetate, dimethylbenzyl-carbinyl acetate, Phenylethyl acetate, linalyl benzoate, benzyl formate, ethyl methyl phenyl glycinate, Allyl cyclohexyl propionate, styrallyl propionate and benzyl salicylate. The ethers include, for example, benzyl ethyl ether, too the aldehydes z. B. the linear alkanals with 8-18C atoms, citral, Citronellal, Citronellyloxyacetaldehyde, Cyclamenaldehyde, Hydroxycitronellal, Lilial and Bourgeonal, to the ketones z. As the Jonone, α-Isomethylionon and methyl cedryl ketone, to the alcohols anethole, citronellol, eugenol, Geraniol, linalool, phenylethyl alcohol and terpineol, to the hydrocarbons are mainly the terpenes like limonene and pinas. However, mixtures of different fragrances are preferred used, which together create an appealing scent. Such Perfume oils can also be natural Fragrance mixtures contain as accessible from plant sources are, for. Pine, citrus, jasmine, patchouly, rose or ylang-ylang oil. Also suitable are muscatel, sage oil, chamomile oil, Clove oil, lemon balm oil, mint oil, cinnamon leaf oil, Lime blossom oil, juniper berry oil, vetiver oil, Olibanum oil, galbanum oil and labdanum oil and orange blossom oil, neroliol, orange peel oil and sandalwood oil.

The compositions according to the invention may contain UV absorbers which are applied to the treated textiles and improve the lightfastness of the fibers and / or the lightfastness of other constituents of the formulation. Under UV absorbers are organic substances (sunscreen) to understand, which are able to absorb ultraviolet rays and the absorbed energy in the form of longer-wave radiation, eg. B. to give off heat again. Compounds having these desired properties include, for example, the non-radiative deactivation compounds and derivatives of benzophenone having substituents in the 2- and / or 4-position. In addition, substituted benzotriazoles, such as the water-soluble benzenesulfonic acid-3- (2H-benzotriazol-2-yl) -4-hydroxy-5- (methylpropyl) monosodium salt (Ciba ^® Fast H), phenyl-substituted in the 3-position acrylates (cinnamic acid derivatives) , optionally with cyano groups in the 2-position, salicylates, organic Ni complexes and natural substances such as umbelliferone and the body's urocanic acid suitable. The biphenyl and especially stilbene derivatives, as are commercially available as Tinosorb ^® FD or Tinosorb ^® FR available ex Ciba. As UV-B absorber are to call 3-Benzylidencampher or 3-Benzylidennorcampher and its derivatives, eg. B. 3- (4-methylbenzylidene) camphor; 4-aminobenzoic acid derivatives, preferably 2-ethylhexyl 4- (dimethylamino) benzoate, 2-octyl 4- (dimethylamino) benzoate and 4- (dimethylamino) benzoic acid ester; Esters of cinnamic acid, preferably 4-methoxycinnamic acid 2-ethylhexyl ester, 4-methoxycinnamic acid propyl ester, 4-methoxycinnamic acid isoamyl ester, 2-cyano-3,3-phenylcinnamic acid 2-ethylhexyl ester (octocrylene); Esters of salicylic acid, preferably 2-ethylhexyl salicylate, 4-isopropylbenzyl salicylate, homomenthyl salicylate; Derivatives of benzophenone, preferably 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone; Esters of benzalmalonic acid, preferably di-2-ethylhexyl 4-methoxybenzmalonate; Triazine derivatives, such as. 2,4,6-trianilino- (p-carbo-2'-ethyl-1'-hexyloxy) -1,3,5-triazine and octyl triazone, as described in U.S.P. EP 0818450 A1 or dioctyl butamido triazone (Uvasorb® HEB); Propane-1,3-diones, such as. B. 1- (4-tert-butylphenyl) -3- (4'-methoxyphenyl) propane-1,3-dione; Ketotricyclo (5.2.1.0) decane derivatives ,. Also suitable are 2-phenylbenzimidazole-5-sulfonic acid and its Al potassium, alkaline earth, ammonium, alkylammonium, alkanolammonium and glucammonium salts; Sulfonic acid derivatives of benzophenones, preferably 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid and its salts; Sulfonic acid derivatives of 3-Benzylidencamphers, such as. B. 4- (2-oxo-3-bornylidenemethyl) benzenesulfonic acid and 2-methyl-5- (2-oxo-3-bomylidene) sulfonic acid and salts thereof.

As a typical UV-A filter in particular derivatives of benzoylmethane are suitable, such as 1- (4'-tert-butylphenyl) -3- (4'-methoxyphenyl) propane-1,3-dione, 4-tert-butyl 4'-methoxydibenzoylmethane (Parsol 1789), 1-phenyl-3- (4'-isopropylphenyl) propane-1,3-dione and enamine compounds. The UV-A and UV-B filters can also be used in mixtures. In addition to the soluble substances mentioned, insoluble photoprotective pigments, namely finely dispersed, preferably nano-metal oxides or salts, are also suitable for this purpose. Examples of suitable metal oxides are in particular zinc oxide and titanium dioxide and, in addition, oxides of iron, zirconium, silicon, manganese, aluminum and cerium and mixtures thereof. As salts silicates (talc), barium sulfate or zinc stearate can be used. The particles should have an average diameter of less than 100 nm, preferably between 5 and 50 nm and in particular between 15 and 30 nm. They may have a spherical shape, but it is also possible to use those particles which have an ellipsoidal or otherwise deviating shape from the spherical shape. The pigments can also be surface-treated, ie hydrophilized or hydrophobized. Typical examples are coated titanium dioxides, such as. Example, titanium dioxide T 805 (Degussa) or Eusolex ^® T2000 (Merck). Suitable hydrophobic coating agents are in particular silicones and in particular trialkoxyoctylsilanes or simethicones. Preferably, micronized zinc oxide is used. UV absorbers are usually used in amounts of from 0.01% by weight to 5% by weight, preferably from 0.03% by weight to 1% by weight.

The agents of the invention may be of assistance the corresponding effect of the invention used Active ingredient's additional anti-crease agents contain since textile fabrics, in particular of rayon, wool, Cotton and their blends tend to be creased can because the individual fibers against sagging, kinking, Pressing and squeezing especially sensitive to the grain direction are. These include, for example, synthetic products based on fatty acids, fatty acid esters, Fatty acid amides, alkylol esters, alkylolamides or fatty alcohols, which are mostly reacted with ethylene oxide, or products on the Base of lecithin or modified phosphoric acid ester.

The agents according to the invention may be graying inhibitors contain. These have the task, the detached from the fiber Keeping dirt suspended in the fleet and so rebuilding to prevent the dirt. These are water-soluble Colloids mostly organic nature suitable, such as glue, Gelatin, salts of ether sulphonic acids or the cellulose or salts of acidic sulfuric acid esters cellulose or starch. Also water-soluble, Acidic group-containing polyamides are for this purpose suitable. Furthermore, can be soluble starch preparations and use other than the above starch products, z. As degraded starch, aldehyde levels, etc. Also Polyvinylpyrrolidone is useful. However, preference is given to anionic or nonionic cellulose ethers such as carboxymethylcellulose (Na salt), Methylcellulose, hydroxyalkylcellulose and mixed ethers such as methylhydroxyethylcellulose, Methylhydroxypropylcellulose and / or methylcarboxymethylcellulose.

In a particularly preferred embodiment are the Fabric care agents according to the invention, preferably Liquid detergent, as a portion in whole or in part water-soluble coating. The portioning makes it easier for the consumer to dose.

The Textile care agents can be used, for example, in foil bags packed. Pouches made of water-soluble Foil rupture of the package by the consumer unnecessary. In this way is a convenient dosing one single, sized for a wash portion by Insert the bag directly into the washing machine or by throwing it in of the bag in a certain amount of water, for example in one Buckets, a bowl or in a hand basin, possible. The foil pouch surrounding the washing portion releases on reaching a certain temperature without residue on.

Numerous processes for the preparation of water-soluble detergent portions, which are basically also useful in the context of the present invention, already exist in the prior art. The best known methods are the tubular film processes with horizontal and vertical sealing seams. Further suitable for the production of film bags or dimensionally stable detergent portions is the Thermoformverrfahren (thermoforming process). However, the water-soluble coatings do not necessarily consist of a film material, but can also form dimensionally stable containers, for example, with Can be obtained by means of an injection molding process.

Furthermore, methods for producing water-soluble capsules of polyvinyl alcohol or gelatin are known, which in principle offer the possibility to provide capsules with a high degree of filling. The methods are based on introducing the water-soluble polymer into a shaping cavity. The filling and sealing of the capsules takes place either synchronously or in successive steps, in which case the filling of the capsules takes place through a small opening in the latter case. Processes in which the filling and sealing are parallel, for example, in the WO 97/35537 described. The filling of the capsules is carried out by a Befüllkeil, which is above two mutually rotating drums, which have ball half shells on its surface, is arranged. The drums carry polymer bands that cover the ball half-shell cavities. At the positions where the polymer band of one drum coincides with the polymer tape of the opposite drum, a seal takes place. In parallel, the filling material is injected into the forming capsule, wherein the injection pressure of the filling liquid presses the polymer bands in the Kugelhalbschalenkavitäten. A process for the preparation of water-soluble capsules, in which initially the filling and then the sealing takes place, is based on the so-called Bottle-Pack ^® method. In this case, a tubular preform is guided into a two-part cavity. The cavity is closed, the lower tube portion is sealed, then the tube is inflated to form the capsule shape in the cavity, filled and finally sealed.

The for the preparation of the water-soluble portion used shell material is preferably a water-soluble polymeric thermoplastic, more preferably selected from the group (optionally partially acetalised) polyvinyl alcohol, Polyvinyl alcohol copolymers, polyvinylpyrrolidone, polyethylene oxide, Gelatin, cellulose and their derivatives, starch and their derivatives Derivatives, blends and composites, inorganic salts and mixtures the materials mentioned, preferably hydroxypropylmethylcellulose and / or polyvinyl alcohol blends.

The polyvinyl alcohols described above are commercially available, for example under the trade name Mowiol ^® (Clariant). In the present OF INVENTION dung particularly suitable polyvinyl alcohols are, for example, Mowiol ^® 3-83, Mowiol ^® 4-88, Mowiol ^® 5-88, Mowiol ^® 8-88 and Clariant L648.

The water-soluble thermoplastic used to prepare the portion may additionally optionally comprise polymers selected from the group comprising acrylic acid-containing polymers, polyacrylamides, oxazoline polymers, polystyrene sulfonates, polyurethanes, polyesters, polyethers and / or mixtures of the above polymers. It is preferred if the water-soluble thermoplastic used comprises a polyvinyl alcohol whose degree of hydrolysis makes up 70 to 100 mol%, preferably 80 to 90 mol%, particularly preferably 81 to 89 mol% and in particular 82 to 88 mol%. More preferably, the water-soluble thermoplastic used comprises a polyvinyl alcohol whose molecular weight is in the range of 10,000 to 100,000 gmol ^-1 , preferably 11,000 to 90,000 gmol ^-1 , more preferably 12,000 to 80,000 gmol ^-1 and especially 13,000 to 70,000 gmol ^-1 lies. It is further preferred if the thermoplastics are used in amounts of at least 50% by weight, preferably of at least 70% by weight, more preferably of at least 80% by weight and in particular of at least 90% by weight, based in each case on the weight the water-soluble polymeric thermoplastic. The polymeric thermoplastics may contain plasticizing aids to improve their machinability. This may be advantageous in particular if polyvinyl alcohol or partially hydrolyzed polyvinyl acetate has been chosen as the polymer material for the portion. Glycerol, triethanolamine, ethylene glycol, propylene glycol, diethylene or dipropylene glycol, diethanolamine and methyldiethylamine have proved particularly suitable as plasticizing auxiliaries. It is advantageous if the polymeric thermoplastics plasticizing in amounts of at least> 0 wt .-%, preferably of ≥ 10 wt .-%, particularly preferably of ≥ 20 wt .-% and in particular of ≥ 30 wt .-%, each based on the weight of the wrapping material.

Further Objects of the invention are the uses of an active ingredient to be used according to the invention in a fabric care product to improve water absorption and / or for improving the shape retention of textile fabrics.

One Another object of the invention is the use of an active ingredient to be used according to the invention in a textile care product to reduce linting.

One Another object of the invention is the use of an active ingredient to be used according to the invention in a textile care product to reduce pilling textile Sheet.

One Another object of the invention is the use of an active ingredient to be used according to the invention in a textile care product for easier ironing textile Sheet.

Surprised was also found that the invention used according to Active ingredients not only reduce wrinkling and for provide a smooth textile surface, but in addition significantly improve the softness of the treated textiles.

One Another object of the invention is therefore the use of a According to the invention to be used drug in one Textile care products for wrinkle reduction, smoothing and Improvement of the softness of textile fabrics.

One Another object of the invention is a conditioning substrate, which is a substrate that is compatible with the invention Textile care impregnated and / or soaked is.

The Substrate material consists of porous materials, which in capable of reversible an impregnating liquid to give up and leave. In question are three-dimensional Structures, such as sponges, but preferably porous, flat cloths. You can made of a fibrous or cellular flexible material consist of sufficient thermal stability for use in the dryer and sufficient quantities of an impregnation or coating agent can hold back to To effectively condition substances without causing damage during the Storage a significant leakage or bleeding of the agent he follows. These towels include cloths woven and unwoven synthetic and natural Fibers, felt, paper or foam, such as hydrophilic polyurethane foam.

Preferably, conventional cloths of nonwoven material (nonwovens) are used here. Nonwovens are generally defined as adhesively bonded fibrous products having a mat or layered fibrous structure, or those comprising fibrous mats in which the fibers are randomly or randomly distributed. The fibers may be of natural origin, such as wool, silk, jute, hemp, cotton, linen, sisal or ramie; or synthetically produced, such as rayon, cellulose esters, polyvinyl derivatives, polyolefins, polyamides, viscose or polyester. In general, any fiber diameter or titer is suitable for the present invention. Preferred conditioning substrates according to the invention consist of a nonwoven material which contains cellulose. The nonwoven fabrics employed herein tend not to rupture or disintegrate due to the random or random arrangement of fibers in the nonwoven material which impart excellent strength in all directions when used, for example, in a household tumble dryer. Preferred porous and flat conditioning cloths consist of one or different fiber materials, in particular of cotton, refined cotton, polyamide, polyester or mixtures of these. The conditioning substrates in fabric form preferably have an area of from 0.2 to 0.005 m ² , preferably from 0.15 to 0.01 m ² , in particular from 0.1 to 0.03 cm ² and particularly preferably from 0.09 to 0, 06 m ² up. The grammage of the material is usually between 20 and 500 g / m ² , preferably from 25 to 200 g / m ² , in particular from 30 to 100 g / m ² and particularly preferably from 40 to 80 g / m ² .

One Another object of the invention is a conditioning method for conditioning wet textiles by means of the invention Conditioning substrate.

The Conditioning process is carried out by the inventive Conditioning substrate together with wet textiles, for example from a previous washing process, in a textile drying process is used. The textile drying process usually takes place in a device for drying textiles, preferably in a household tumble dryer instead.

Further Objects of the invention are methods of reduction linting, to reduce pilling, ironing, for crease reduction, smoothing and / or improvement the soft grip of textile fabrics by contacting textile surface image with an inventive Textile care agents and / or an inventive Conditioning substrate in a textile cleaning process and / or Textile drying process.

The Fabric care agents according to the invention can in their conditioning aspect directly with the wet laundry placed in a household dryer and / or a washing machine become.

The textile care compositions according to the invention can be prepared by simple mixing and stirring of the individual components familiar to the person skilled in the art. Use according to the invention The active compounds can be used as such or as a solution or slurry, preferably in aqueous form, a particular liquid agent are mixed and / or as a solid, for example powder, preferably applied to a detergent ingredient as a carrier, compounded or granulated, mixed or tableted or pelleted.

Examples

Example 1: Softness

• a) Washing conditions Washer: Miele W 918 Washing program: single-leaching Koch-Hunt program Washing temperature: 40 ° C Fleet volume: 171 Water hardness: 16 ° dH Filling laundry: 3,5kg clean Laundry incl. Test fabric (pillow, jersey, tableware, Stye towels) Test fabric: Terry disposable towels (100% Cotton)
• b) Procedure: The textiles were washed 1x and 3x one described in the following table in its composition Washing agent washed under the conditions given above and air dried after each wash. After the third wash For example, the softness of the test fabric was experienced by one group Subjects were determined sensory compared to standards.

Detergent compositions [wt%]: C _12-14 fatty alcohol with 7 EO 5 4 10 C _9-13 alkyl benzene sulphonate, Na salt 10 10 10 Sodium lauryl ether sulfate with 2 EO - - 8th Substance essential to the invention 1 1 1 polyacrylate - - 1 sodium 15 18 - TAED 3 3 - C _12-18 fatty acid, Na salt 1 1.5 7.5 PVA / maleic acid copolymer 4.5 2 - Citric acid, Na salt 2.5 - 2 Phosphonic acid, Na salt 0.5 0.5 1 sodium 10 20 - propanediol - - 6.5 Zeolite A 25 25 - Boric acid, Na salt - - 1.2 Silicone antifoam 2.5 1.3 0.1 Enzymes (amylase, protease, cellulase) + + + dye + + + Perfume 0.5 0.2 0.8 water - - Ad 100 sodium sulphate - Ad 100 - sodium bicarbonate Ad 100 - -

• c) Results From 30 subjects felt the main proportion of persons the test tissue, the was treated with a detergent containing the active ingredient, as softer compared to a test tissue, which only with the otherwise identical detergent composition was treated, the drug was missing.

Example 2: elasticity

• a) Washing conditions Washer: Miele W 918 Washing program: single-lye procedure normal program Washing temperature: 40 ° C Fleet volume: 171 Water hardness: 16 ° dH Linen: 2 kg clean Laundry Fabric: 100% Cotton Sweater; Sweater 76% Cotton finished / 19% polyamide / 5% elastane
• b) Implementation: The textiles were washed 10 times with the in Example 1 detergents described above Washed conditions and dried after each wash. After washing 10 times, the textiles were 80% of the original Length stretched for a minute, then followed by one Relaxation time of 3 minutes and finally the measurement the remaining stretch.
• c) strain results The 10x with a detergent, which the active ingredient, washed textiles showed a significant lower residual strain than that with the otherwise equal composition Detergent lacking the active ingredient washed textile.

QUOTES INCLUDE IN THE DESCRIPTION

This list The documents listed by the applicant have been automated generated and is solely for better information recorded by the reader. The list is not part of the German Patent or utility model application. The DPMA takes over no liability for any errors or omissions.

Cited patent literature

• WO 99/16956 A1 [0003]
• WO 00/77134 [0004]
• - DE 10203192 A1 [0005]
• WO 2005/058863 [0012]
• - JP 58/217598 [0030]
• WO 90/13533 A [0030]
• - DE 4321022 A [0032]
• WO 96/23768 A [0032]
• DE 19513391 A [0032]
• WO 95/19953 A [0033]
• WO 95/19954 A [0033]
• WO 95/19955 A [0033]
• WO 95/07331 A [0035]
• US 3234258 [0041]
• - US 5075041 [0041]
• - EP 0818450 A1 [0128]
• WO 97/35537 [0135]

Claims (17)

Textile care compositions containing an active substance selected from the compounds of general formulas I or II,

wherein R is C ₁ -C ₁₂ alkylene; k is a number greater than 0, X is CO-CH = CH ₂ , CO-C (CH ₃ ) = CH ₂ , CO-O-aryl, C ₂ -C ₆ -alkylene-SO ₂ -CH = CH ₂ , or CO-NH-R ¹ ; and R ^{1 is} C ₁ -C ₃₀ -alkyl, C ₁ -C ₃₀ -haloalkyl, C ₁ -C ₃₀ -hydroxyalkyl, C ₁ -C ₆ -alkyloxy-C ₁ -C ₃₀ -alkyl, C ₁ -C ₆ - Alkylcarbonyloxy-C ₁ -C ₃₀ -alkyl, amino-C ₁ -C ₃₀ -alkyl, mono- or di (C ₁ -C ₆ -alkyl) amino-C ₁ -C ₃₀ -alkyl, ammonio-C ₁ -C ₃₀ alkyl, polyoxyalkylene C ₁ -C ₃₀ alkyl, polysiloxanyl C ₁ -C ₃₀ alkyl, (meth) acryloyloxy C ₁ -C ₃₀ alkyl, sulfono C ₁ -C ₃₀ alkyl, phosphonoC ₁ -C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphono C ₁ -C ₃₀ alkyl, phosphonato C ₁ -C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphonato-C C ₁ -C ₃₀ -alkyl or a saccharide radical, where in formula IX this meaning has only if k is 1, or X is (i) the radical of a polyamine to which the parenthesized formula part on (CO) NH Or (ii) a polymeric backbone to which the parenthesized part of the formula is attached via (CO) -, NH-C ₂ -C ₆ -alkylene-O (CO) - or (CO) -OC ₂ -C ₆ -alkylene-O (CO) groups, or (iii) a polymeric backbone to which the parenthesis standing formula part is bound via (CO) -polysiloxanyl-C ₁ -C ₃₀ -alkyl groups, when k is a number greater than 1, and polymers which are obtainable by reacting a polymeric substrate having functional groups which are selected from hydroxy groups, primary and secondary amino groups, with a compound of the general formulas I or II. Means according to claim 1, characterized in that the compound of formula I is selected 4-phenyloxycarbonyloxymethyl-2-oxo-1,3-dioxolane, 4- (4-Phenyloxycarbonyloxy) butyl-2-oxo-1,3-dioxolane, 2-oxo-1,3 dioxolan-4-yl-methyl, 2-oxo-1,3-dioxolan-4-yl-methyl, 4- (2-oxo-1,3-dioxolan-4-yl) butyl acrylate, 4- (2-oxo-1,3-dioxolan-4-yl) butyl methacrylate and 4- (Vinylsulfonylethyloxy) butyl-2-oxo-1,3-dioxolane. Agent according to claim 1 or 2, characterized that the polymeric substrate is selected from the group including polyvinyl alcohols, polyalkylene amines such as polyethyleneimine, Polyvinylamines, polyallylamines, polyethylene glycols, chitosan, polyamide-epichlorohydrin resins, Polyaminostyrenes, with aminoalkyl groups terminal or as a side group substituted polysiloxanes, peptides, polypeptides, and proteins and their Mixtures. Composition according to one of claims 1 to 3, characterized in that the polymeric substrate is selected from the polyethyleneimines having molecular weights in the range of 5,000 to 100,000, compounds of the formula NH ₂ - [CH ₂ ] _m - (Si (CH ₃ ) ₂ O) _n Si (CH ₃ ) ₂ - [CH ₂ ] _o -R ', where m = 1 to 10, preferably 1 to 5, particularly preferably 1 to 3, where n = 1 to 50, preferably 30 to 50 where 0 = 0 to 10, preferably 1 to 5, particularly preferably 1 to 3 and wherein R '= H, C _1-22- alkyl, an amino or ammonium group, and compounds of the formula NH ₂ - [CH (CH ₃ ) -CH ₂ O] ₁ - [CH ₂ -CH ₂ O] _m [CH ₂ -CH (CH ₃ ) O] _n R ", where 1, m and n are independently from 0 to 50 are provided with the proviso that the sum of 1 + m + n = 5 to 100, in particular 10 to 50, preferably 10 to 30, particularly preferably 10 to 20, and R '' = H, a C _1-22 alkyl -, C _1-22 -Aminoalkyl- or C _1-22 -ammoniumalkyl group, and mixtures thereof. Composition according to claim 1, characterized in that the active ingredient of the polycarbonate and / or polyurethane-polyorganosiloxane compounds containing at least one structural element of the formula (III): -AYA- (CO) -OZ- (CHORO) -ZO- (CO) - (III), wherein A is selected from -O-, -S- and -NR ² -, Y is selected from di- to polyvalent, especially tetravalent, straight-chain, cyclic or branched, saturated, unsaturated or aromatic, substituted or unsubstituted hydrocarbon radicals having up to 1000 Carbon atoms which may contain one or more groups selected from -O-, - (CO) -, -NH-, -NR ² -, - (N ⁺ R ³ R ⁴ ) - and a polyorganosiloxane unit having 2 to 1000 silicon atoms, Z is selected from the divalent, straight-chain, cyclic or branched, saturated or unsaturated, optionally substituted hydrocarbon radicals having 1 to 12 carbon atoms, R ^{2 is} hydrogen or a straight-chain, cyclic or branched, saturated, unsaturated or aromatic hydrocarbon radical having up to 40 carbon atoms, which may contain one or more groups selected from -O-, - (CO) -, -NH- and -NR ³ -, R ^{3 is} a straight-chain, cyclic or is a branched, saturated, unsaturated or aromatic hydrocarbon radical having up to 40 carbon atoms, which may contain one or more groups selected from -O-, - (CO) - and -NH-, R ^{4 is} a straight-chain, cyclic or branched, saturated, unsaturated or aromatic hydrocarbon radical having up to 100 carbon atoms, which may contain one or more groups selected from -O-, - (CO) - and -NH-, or is a bivalent radical which forms cyclic structures within the radical Y, or one or both of the radicals Y adjacent to Y can form a nitrogen-containing heterocyclic radical with the radical Y between them, and in the overall compound not all of the radicals A, Y, Z or R ² indicated in formula (III) R ³ or R ⁴ must be identical, with the proviso that in the entire compound at least one of the radicals Y comprises a polyorganosiloxane unit having 2 to 1000 silicon atoms, as well as their Säuread tion compounds and / or salts is selected. Agent according to one of claims 1 to 5, characterized in that it is 0.1 wt .-% to 5 wt .-%, in particular 0.1 wt .-% to 1 wt .-% of the active ingredient. Agent according to one of claims 1 to 6, characterized in that it complexing agents, in particular organic, advantageously water-soluble, complexing agents, particularly preferred acid group-containing coplexing agent, extremely preferably citric acid and / or its alkali metal salts contains. Agent according to one of claims 1 to 7, characterized in that it is in solid form, preferably as Powder, granules, extrudate, pressed and / or melted shaped body or as a tablet, particularly preferably in liquid form, in particular as a dispersion, suspension, emulsion, solution, Microemulsion, gel or paste is present. Agent according to one of claims 1 to 8, characterized in that it is enzyme, preferably selected from the group of proteases and / or amylases and / or cellulases, contains. Agent according to one of claims 1 to 9, characterized in that it as a portion in a whole or partially water-soluble envelope is present. Use of compounds of the general formulas I or II,

wherein R is C ₁ -C ₁₂ alkylene; k is a number greater than 0, X is CO-CH = CH ₂ , CO-C (CH ₃ ) = CH ₂ , CO-O-aryl, C ₂ -C ₆ -alkylene-SO ₂ -CH = CH ₂ , or CO-NH-R ¹ ; and R ^{1 is} C ₁ -C ₃₀ -alkyl, C ₁ -C ₃₀ -haloalkyl, C ₁ -C ₃₀ -hydroxyalkyl, C ₁ -C ₆ -alkyloxy-C ₁ -C ₃₀ -alkyl, C ₁ -C ₆ - Alkylcarbonyloxy-C ₁ -C ₃₀ -alkyl, amino-C ₁ -C ₃₀ -alkyl, mono- or di (C ₁ -C ₆ -alkyl) amino-C ₁ -C ₃₀ -alkyl, ammonio-C ₁ -C ₃₀ alkyl, polyoxyalkylene C ₁ -C ₃₀ alkyl, polysiloxanyl C ₁ -C ₃₀ alkyl, (meth) acryloyloxy C ₁ -C ₃₀ alkyl, sulfono C ₁ -C ₃₀ alkyl, phosphonoC ₁ C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphono C ₁ -C ₃₀ alkyl, phosphonato C ₁ -C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphonato C ₁ C ₃₀ alkyl or a saccharide radical, where in formula IX this meaning has only if k is 1, or X is (i) the radical of a polyamine to which the parenthesized formula part is divided by (CO) NH- Or (ii) a polymeric backbone to which the parenthetical formula portion is attached via (CO) -, NH-C ₂ -C ₆ -alkylene-O (CO) - or (CO) -OC ₂ -C ₆ Alkylene-O (CO) groups, or (iii) a polymeric backbone to which the parenthesis wherein the formula is bonded via (CO) polysiloxanyl-C ₁ -C ₃₀ -alkyl groups, when k is a number greater than 1, or from polymers which are obtainable by reacting a polymeric substrate which is functional Has groups which are selected from hydroxy groups, primary and secondary amino groups, with a compound of general formulas I or II, in a fabric care agent to improve the water absorption of fabrics. Use of compounds of the general formulas I or II,

wherein R is C ₁ -C ₁₂ alkylene; k is a number greater than 0, X is CO-CH = CH ₂ , CO-C (CH ₃ ) = CH ₂ , CO-O-aryl, C ₂ -C ₆ -alkylene-SO ₂ -CH = CH ₂ , or CO-NH-R ¹ ; and R ^{1 is} C ₁ -C ₃₀ -alkyl, C ₁ -C ₃₀ -haloalkyl, C ₁ -C ₃₀ -hydroxyalkyl, C ₁ -C ₆ -alkyloxy-C ₁ -C ₃₀ -alkyl, C ₁ -C ₆ - Alkylcarbonyloxy-C ₁ -C ₃₀ -alkyl, amino-C ₁ -C ₃₀ -alkyl, mono- or di (C ₁ -C ₆ -alkyl) amino-C ₁ -C ₃₀ -alkyl, ammonio-C ₁ -C ₃₀ alkyl, polyoxyalkylene C ₁ -C ₃₀ alkyl, polysiloxanyl C ₁ -C ₃₀ alkyl, (meth) acryloyloxy C ₁ -C ₃₀ alkyl, sulfono C ₁ -C ₃₀ alkyl, phosphonoC ₁ C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphono C ₁ -C ₃₀ alkyl, phosphonato C ₁ -C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphonato C ₁ C ₃₀ alkyl or a saccharide radical, where in formula IX this meaning has only if k is 1, or X is (i) the radical of a polyamine to which the parenthesized formula part is divided by (CO) NH- Or (ii) a polymeric backbone to which the parenthetical formula portion is attached via (CO) -, NH-C ₂ -C ₆ -alkylene-O (CO) - or (CO) -OC ₂ -C ₆ Alkylene-O (CO) groups, or (iii) a polymeric backbone to which the parenthesis wherein the formula is bonded via (CO) polysiloxanyl-C ₁ -C ₃₀ -alkyl groups, when k is a number greater than 1, or from polymers which are obtainable by reacting a polymeric substrate which is functional Groups which are selected from hydroxy groups, primary and secondary amino groups with a compound of the general formulas I or II in a textile care agent for improving the shape retention of textile fabrics. Use of compounds of the general formulas I or II,

wherein R is C ₁ -C ₁₂ alkylene; k is a number greater than 0, X is CO-CH =CH ₂ , CO-C (CH ₃ ) CHCH ₂ , CO-O-aryl, C ₂ -C ₆ -alkylene-SO ₂ -CH = CH 2, or CO-NH-R ¹ ; and R ^{1 is} C ₁ -C ₃₀ -alkyl, C ₁ -C ₃₀ -haloalkyl, C ₁ -C ₃₀ -hydroxyalkyl, C ₁ -C ₆ -alkyloxy-C ₁ -C ₃₀ -alkyl, C ₁ -C ₆ - Alkylcarbonyloxy-C ₁ -C ₃₀ -alkyl, amino-C ₁ -C ₃₀ -alkyl, mono- or di (C ₁ -C ₆ -alkyl) amino-C ₁ -C ₃₀ -alkyl, ammonio-C ₁ -C ₃₀ alkyl, polyoxyalkylene C ₁ -C ₃₀ alkyl, polysiloxanyl C ₁ -C ₃₀ alkyl, (meth) acryloyloxy C ₁ -C ₃₀ alkyl, sulfono C ₁ -C ₃₀ alkyl, phosphonoC ₁ C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphono C ₁ -C ₃₀ alkyl, phosphonato C ₁ -C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphonato C ₁ C ₃₀ alkyl or a saccharide radical, where in formula IX this meaning has only if k is 1, or X is (i) the radical of a polyamine to which the parenthesized formula part is divided by (CO) NH- Or (ii) a polymeric backbone to which the parenthetical formula portion is attached via (CO) -, NH-C ₂ -C ₆ -alkylene-O (CO) - or (CO) -OC ₂ -C ₆ Alkylene-O (CO) groups, or (iii) a polymeric backbone to which the parenthesis wherein the formula is bonded via (CO) polysiloxanyl-C ₁ -C ₃₀ -alkyl groups, when k is a number greater than 1, or from polymers which are obtainable by reacting a polymeric substrate which is functional Has groups which are selected from hydroxy groups, primary and secondary amino groups, with a compound of general formulas I or II in a textile care agent to reduce linting. Use of compounds of the general formulas 1 or II,

wherein R is C ₁ -C ₁₂ alkylene; k is a number greater than 0, X is CO-CH = CH ₂ , CO-C (CH ₃ ) = CH ₂ , CO-O-aryl, C ₂ -C ₆ -alkylene-SO ₂ -CH = CH ₂ , or CO-NH-R ¹ ; and R ^{1 is} C ₁ -C ₃₀ -alkyl, C ₁ -C ₃₀ -haloalkyl, C ₁ -C ₃₀ -hydroxyalkyl, C ₁ -C ₆ -alkyloxy-C ₁ -C ₃₀ -alkyl, C ₁ -C ₆ - Alkylcarbonyloxy-C ₁ -C ₃₀ -alkyl, amino-C ₁ -C ₃₀ -alkyl, mono- or di (C ₁ -C ₆ -alkyl) amino-C ₁ -C ₃₀ -alkyl, ammonio-C ₁ -C ₃₀ alkyl, polyoxyalkylene C ₁ -C ₃₀ alkyl, polysiloxanyl C ₁ -C ₃₀ alkyl, (meth) acryloyloxy C ₁ -C ₃₀ alkyl, sulfono C ₁ -C ₃₀ alkyl, phosphonoC ₁ C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphono C ₁ -C ₃₀ alkyl, phosphonato C ₁ -C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphonato C ₁ C ₃₀ -alkyl or a saccharide radical, where in formula IX this meaning has only if k is 1, or X is (i) the radical of a polyamine to which the formula part in parentheses is attached via (CO) NH-- Or (ii) a polymeric backbone to which the parenthetical formula part is attached via (CO) -, NH-C ₂ -C ₆ -alkylene-O (CO) - or (CO) -OC ₂ -C ₆ -alkylene-O (CO) groups, or (iii) a polymeric backbone to which the parenthesized formula part is attached via (CO) -polysiloxanyl-C ₁ -C ₃₀ - alkyl groups is attached, if k is a number greater than 1, or of polymers which are obtainable by reacting a polymeric substrate having functional groups which are selected from hydroxy groups, primary and secondary amino groups, with a compound of the general formulas I or II in a textile care agent for reducing the pilling of textile fabrics. Use of compounds of the general formulas I or II,

wherein R is C ₁ -C ₁₂ alkylene; k is a number greater than 0, X is CO-CH = CH ₂ , CO-C (CH ₃ ) = CH ₂ , CO-O-aryl, C ₂ -C ₆ -alkylene-SO ₂ -CH = CH ₂ , or CO-NH-R ¹ ; and R ^{1 is} C ₁ -C ₃₀ -alkyl, C ₁ -C ₃₀ -haloalkyl, C ₁ -C ₃₀ -hydroxyalkyl, C ₁ -C ₆ -alkyloxy-C ₁ -C ₃₀ -alkyl, C ₁ -C ₆ - Alkylcarbonyloxy-C ₁ -C ₃₀ -alkyl, amino-C ₁ -C ₃₀ -alkyl, mono- or di (C ₁ -C ₆ -alkyl) amino-C ₁ -C ₃₀ -alkyl, ammonio-C ₁ -C ₃₀ alkyl, polyoxyalkylene C ₁ -C ₃₀ alkyl, polysiloxanyl C ₁ -C ₃₀ alkyl, (meth) acryloyloxy C ₁ -C ₃₀ alkyl, sulfono C ₁ -C ₃₀ alkyl, phosphonoC ₁ C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphono C ₁ -C ₃₀ alkyl, phosphonato C ₁ -C ₃₀ alkyl, di (C ₁ -C ₆ alkyl) phosphonato C ₁ C ₃₀ alkyl or a saccharide radical, where in formula IX this meaning has only if k is 1, or X is (i) the radical of a polyamine to which the parenthesized formula part is divided by (CO) NH- Or (ii) a polymeric backbone to which the parenthetical formula portion is attached via (CO) -, NH-C ₂ -C ₆ -alkylene-O (CO) - or (CO) -OC ₂ -C ₆ Alkylene-O (CO) groups, or (iii) a polymeric backbone to which the parenthesis wherein the formula is bonded via (CO) polysiloxanyl-C ₁ -C ₃₀ -alkyl groups, when k is a number greater than 1, or from polymers which are obtainable by reacting a polymeric substrate which is functional Has groups which are selected from hydroxy groups, primary and secondary amino groups, with a compound of general formulas I or II in a fabric care fabric for easy ironing textile fabrics. Use of compounds of the general formulas I or II,

wherein R is C ₁ -C ₁₂ alkylene; k is a number greater than 0, X is CO-CH = CH ₂ , CO-C (CH ₃ ) = CH ₂ , CO-O-aryl, C ₁ -C ₆ -alkylene-SO ₂ -CH = CH ₂ , or CO-NH-R ¹ ; and R ¹ for C ₁ -C ₃₀ -alkyl, C ₁ -C ₃₀ -haloalkyl, C ₁ -C ₃₀ -hydroxyalkyl, C ₁ -C ₆ -alkyloxy-C ₁ -C ₃₀ -alkyl, C ₁ -C ₆ -alkylcarbonyloxy-C ₁ C ₃₀ alkyl, amino C ₁ -C ₃₀ alkyl, mono- or di (C ₁ -C ₆ alkyl) amino C ₁ -C ₃₀ alkyl, ammonium C ₁ -C ₃₀ alkyl, polyoxyalkylene C ₁ -C ₃₀ -alkyl, polysiloxanyl-C ₁ -C ₃₀ -alkyl, (meth) acryloyloxy-C ₁ -C ₃₀ -alkyl, sulfono-C ₁ -C ₃₀ -alkyl, phosphono-C ₁ -C ₃₀ - alkyl, di (C ₁ -C ₆ -alkyl) phosphonoC ₁ -C ₃₀ -alkyl, phosphonatoC ₁ -C ₃₀ -alkyl, di (C ₁ -C ₆ -alkyl) phosphonatoC ₁ -C ₃₀ - is alkyl or a saccharide radical, where in formula IX this meaning has only if k is 1, or X is (i) the radical of a polyamine to which the parenthesized formula part is bonded via (CO) NH groups, or (ii) a polymeric backbone to which the parenthesized part of the formula is attached via (CO) -, NH-C ₂ -C ₆ -alkylene-O (CO) - or (CO) -OC ₂ -C ₆ -alkylene-O (CO) groups, or (iii) a polymeric backbone to which the parenthesized form part is bound via (CO) -polysiloxanyl-C ₁ -C ₃₀ -alkyl groups, when k is a number greater than 1, or of polymers which are obtainable by reacting a polymeric substrate having functional groups which are selected from hydroxy groups, primary and secondary amino groups, with a compound of the general formulas I or II in a fabric care composition for wrinkle reduction, smoothing and improving the softness of textile fabrics. Method for reducing linting textile Fabrics by contacting textile sheets with a fabric care agent according to one of claims 1 to 10 in a textile cleaning process and / or textile drying process.