WO2018055124A1 - Fast-dissolving perfume-containing soluble body - Google Patents

Abstract

The invention relates to a solid, particulate composition comprising at least one water-soluble carrier polymer, at least one odoriferous substance and at least one compound having a HLB value of ≥ 7. The invention also relates to a washing or cleaning agent that contains the solid composition. The invention further relates to the use of said type of washing or cleaning agent for cleaning textiles or hard surfaces and to corresponding methods for cleaning textiles or hard surfaces using said type of washing or cleaning agent.

Description

 Fast-dissolving, perfume-containing enamel body

The present invention relates to a solid, particulate composition comprising at least one water-soluble carrier polymer, at least one perfume and at least one compound having an HLB value of> 7. Furthermore, the invention relates to a washing or cleaning agent containing the solid composition. Moreover, the present invention also relates to the use of such a washing or cleaning agent for cleaning textiles or hard surfaces and corresponding methods for cleaning textiles or hard surfaces using such a washing or cleaning agent.

In the use of detergents and cleaners, the consumer not only aims to wash, cleanse or care for the objects to be treated, but also desires that the treated objects, e.g. Textiles, after the treatment, for example after the wash, smell pleasant. For this reason in particular, most commercially available detergents and cleaners contain fragrances.

Most of the fragrances, however, are volatile. For this reason, when using conventional washing or cleaning agents after use, especially after washing, only a small proportion of the fragrance used remains on the treated object.

As a result, often only a faint scent of the treated object, especially the laundry, goes out, which then already weaker after a short time. Thus, the pleasant feeling of freshness of the treated object disappears after a short time.

Often fragrances are used in the form of perfume particles either as an integral part of a washing or cleaning agent, or dosed directly into the washing drum at the beginning of a wash cycle in a separate form. In this way, the consumer can control the fragrance of the laundry to be washed by individual dosage.

The use of short and energetically economical, especially cold washes becomes more and more relevant for the consumer. A complete dissolution of perfume particles, in particular those based on carrier polymers such as polyalkylene glycols, in relatively short wash cycles with comparatively little water in the wash liquor and / or in cold wash cycles can, as a rule not guaranteed. Thus, after completion of the washing process, undesirable residues of the fragrance particles in the washing drum are increasingly produced.

There is therefore still a need for detergents and cleaning agents which allow improved object scenting in the objects to be treated, preferably in textiles, and which do not lead to product residues in the washing drum, in particular when used in short and / or cold wash programs.

The object of the present invention was therefore to overcome the above-mentioned problems and at the same time to ensure adequate scenting of the object. The object of the present invention was in particular. To provide detergents and cleaners, after the application, the treated products, preferably textiles, not only clean, but also have an improved fragrance intensity, which persists even over a long period.

The objects were achieved according to the invention by a solid, particulate composition which, in addition to a carrier polymer, comprises one or more perfumes and / or a perfume capsule granule and is distinguished by a good solubility in water.

In a first aspect, therefore, the present invention is directed to a solid, particulate composition comprising at least one water-soluble carrier polymer having a

Melting point> 30 ° C, preferably> 40 ° C, preferably selected from polyalkylene glycols, more preferably polyethylene glycol, and at least one perfume, characterized in that the composition comprises at least one compound with an HLB value of> 7 selected from the group consisting of nonionic surfactants , Anionic surfactants, cationic surfactants and

Amphoteric surfactants for accelerating the solubility of the composition in an aqueous solution.

"Water-soluble" as used herein means a solubility in water at 20 ° C of at least 1 g / L, preferably at least 10 g / L, more preferably at least 50 g / L.

In another aspect, the present invention is directed to the use of the solid composition as described herein as a fabric care, preferably fragrance and / or fabric softener, conditioner and / or conditioner for fabrics.

In yet another aspect, the present invention is further directed to a laundry or cleaning composition comprising a solid composition as described herein. These and other aspects, features, and advantages of the invention will become apparent to those skilled in the art from a study of the following detailed description and claims. Any feature of one aspect of the invention may be employed in any other aspect of the invention. Further, it is to be understood that the examples contained herein are intended to describe and illustrate the invention, but not to limit it, and in particular that the invention is not limited to these examples.

All percentages are by weight unless otherwise specified. Numeric ranges specified in the format "from x to y" include the above values.If multiple preferred numeric ranges are specified in this format, it is understood that all ranges resulting from the combination of the various endpoints, also be recorded.

"At least one" as used herein refers to 1 or more, for example, 1, 2, 3, 4, 5, 6, 7, 8, 9 or more, more particularly, this indication refers to the type of agent / compound and not the absolute number of molecules. "At least one perfume", therefore, means that at least one type of perfume is detected but may also contain 2 or more different types of perfume.

A first object of the present invention is a solid, particulate composition comprising at least one water-soluble carrier polymer having a melting point> 30 ° C, preferably> 40 ° C, preferably selected from polyalkylene glycols, more preferably polyethylene glycol, and at least one perfume, characterized in that

Composition containing at least one compound having an HLB value of> 7 selected from the group consisting of nonionic surfactants, anionic surfactants, cationic surfactants and amphoteric surfactants for accelerating the solubility of the composition in an aqueous solution.

An "aqueous solution" as used herein may be water or a mixture of water with one or more other substances, for example, an aqueous solution may be, in particular, a mechanical one

Washing process resulting wash liquor act.

The HLB value (HLB: hydrophilic-lipophilic balance) is a value that describes the ratio of lipophilic and hydrophilic parts within a molecule.

According to Griffin, the HLB value can be calculated using the following general formula:

HLB = 20 X (1 - Mlipophil / M Total) Here Mii _{P0P hii} denotes the molecular weight of the lipophilic portion of the molecule in question and Mgesamt denotes the molecular weight of the entire molecule, resulting in a scale from 0 to 20 for the HLB value.

For polyalkoxylated fatty alcohols, the HLB value results in particular according to:

 HLB = 20 X (Mhydrophile / total) (II)

Here Mhydrophii denotes the molecular weight of the hydrophilic portion of the molecule in question and Mgesamt denotes the molecular weight of the entire molecule, resulting in a scale of 0 to 20 for the HLB value.

Another method of determination, according to Davies

Here, m denotes the number of hydrophilic groups in the molecule, H h denotes the value of the hydrophilic group, n denotes the number of lipophilic groups in the molecule and Hi denotes the value of the lipophilic group.

The HLB value can be determined for non-ionic compounds according to Griffin, for ionic compounds according to Davies. According to the HLB value for polyalkoxylated compounds of formula (II) is determined.

Based on their HLB value, individual compounds can be divided into different substance classes. Connections with an HLB value in the lower range of the HLB scale, i. below an HLB value of 7, characterized by their relatively pronounced lipophilic character by low to poor or not given miscibility with water.

By using compounds with an HLB value greater than 7 fragrance particles can be prepared, which can be completely dissolved even in short and / or cold wash programs.

According to the present invention, the at least one compound having an HLB value of> 7 is selected from the group consisting of nonionic surfactants (nonionic surfactants),

Anionic surfactants, cationic surfactants and amphoteric surfactants. The group of nonionic surfactants commonly include polyalkoxylated fatty alcohols and

Fatty acid alkyl esters, polyhydroxy fatty acid amides, fatty acid alkanolamides, alkyl glycosides and alkylphenol ethoxylates.

The group of alkyl glycosides includes compounds of the general formula RO (G) x in which R corresponds to a primary straight-chain or methyl-branched, in particular 2-methyl-branched aliphatic radical having 8 to 22, preferably 12 to 18 carbon atoms and G is the symbol which represents a glycose unit having 5 or 6 C atoms, preferably glucose or xylose. The degree of oligomerization x, which indicates the distribution of monoglycosides and oligoglycosides, is an arbitrary number between 1 and 10; preferably x is 1, 2 to 1, 4.

The group of fatty acid alkanolamides includes, for example, without limitation,

Coconut fatty acid monoethanolamide, coconut fatty acid diethanolamide, soybean fatty acid monoethanolamide, soy fatty acid diethanolamide, oleic acid monoethanolamide and oleic acid diethanolamide.

The group of alkylphenol ethoxylates includes octylphenol ethoxylates as well

Nonylphenolethoxylate, wherein the degree of ethoxylation may each be 1 to 25.

The group of alkoxylated, preferably ethoxylated or ethoxylated and propoxylated fatty acid alkyl esters includes, in particular, those fatty acid alkyl esters having 1 to 4

Carbon atoms in the alkyl chain. In general, corresponding compounds represented by the general formula R-COO- (CH ₂ CH ₂ O) x- (CH ₂ CH ₂ CH ₂ O) y R ² , where R is a saturated, monounsaturated or polyunsaturated fatty acid alkyl chain of 6 to 30 carbon atoms, x is an integer of 1 to 50, y represents an integer of 0 to 25, and R ^{2 represents} H or an alkyl group of 1 to 4 carbon atoms. Preferred radicals R are selected from hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl. Pentadecyl, hexadecyl, heptadecyl, octadecyi, nonadecyl, eicosyl and mixtures thereof, with the even number of C atoms being preferred. Particularly preferred radicals R are derived from C 12-18 fatty alcohols, for example from coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or from C 1 -C 24 -oxo alcohols (in particular C 9 -oxo alcohols, C 10 -oxoalcohols, ds-oxoalcohols and or cis-oxo alcohols).

In various embodiments, the sum of x and y is an integer from 1 to 50, preferably from 1 to 30 and especially from 7 to 25. Most preferably, y is 0 and x is a number in the range of 5-25.

Also suitable are nonionic surfactants which have alternating ethylene oxide and alkylene oxide units. Among these, in turn, surfactants with EO-AO-EO-AO blocks are preferred, wherein one to ten EO or AO groups are bound to each other before one block follows from the other groups. Here are nonionic surfactants of the general formula

RHD- (CH ₂ -CH ₂ -O) - (CH ₂ -

in which R is a straight-chain or branched, saturated or mono- or polyunsaturated C 6-24-alkyl or alkenyl radical; each group R ² or R ^{3 is} independently selected from -Chta, -CH 2 CH 3, -CH 2 CH 2 -CH 3, CH (CH 3) 2 and the indices w, x, y, z independently represent integers from 1 to 6.

Thus, particularly suitable are nonionic surfactants having a C9-alkyl group having 1 to 4 ethylene oxide units, followed by 1 to 4 propylene oxide units, followed by 1 to 4

Ethylene oxide units followed by 1 to 4 propylene oxide units.

Other suitable nonionic surfactants are those of the general formula

R is -CH (OH) CH ₂ 0- (AO) w- (A 0) x (A "0) _y - (A" O) z R ² wherein

 R is a straight-chain or branched, saturated or mono- or polyunsaturated C 6-24-alkyl or alkenyl radical;

R ^{2 is} H or a linear or branched hydrocarbon radical having 2 to 26 carbon atoms;

A, Α ', A "and A'" independently of one another are radicals from the group -CH ₂ CH ₂ , -CH ₂ CH ₂ -CH ₂ , -CH ₂ -CH (CH ₃ ), -CH ₂ -CH ₂ -CH ₂ -CH ₂ , -CH ₂ - CH (CH ₃ ) -CH ₂ -, - CH ₂ -CH (CH ₂ -CH ₃ ),

 w, x, y and z are values between 0.5 and 120, where x, y and / or z can also be 0.

The specified C chain lengths and Ethoxylierungsgrade or

Degradation levels of nonionic surfactants represent statistical averages which may be an integer or a fractional number for a particular product. Due to the

Herste II method exist commercial products of the formulas mentioned mostly not from an individual representative, but from mixtures, which may result in both the C chain lengths and for the Ethoxylierungsgrade or degrees of alkoxylation averages and resulting broken numbers. Also suitable in the context of the present invention are anionic surfactants. Anionic surfactants are characterized by a water-solubilizing, anionic group such. Legs

Carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group having about 8 to 30 carbon atoms. In addition, glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups may be present in the molecule. Suitable anionic surfactants are preferably in the form of the sodium, potassium and ammonium as well as the mono-, di- and

Trialkanolammoniumsalze with 2 to 4 carbon atoms in the alkanol group.

Preferred anionic surfactants are alkyl carboxylates, alkyl sulfates, alkyl polyglycol ether sulfates and ether carboxylic acids having 10 to 18 C atoms in the alkyl group and up to 12 glycol ether groups in the molecule.

Particularly suitable are compounds of the formula R ⁴ -O- (AO) _n -SO 3 ^" X ⁺ .

In this formula, R ^{4 is} a linear or branched, substituted or unsubstituted alkyl, aryl or alkylaryl radical, preferably a linear, unsubstituted alkyl radical, more preferably a fatty alcohol radical. Preferred radicals R are selected from decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl radicals and mixtures thereof, the representatives having an even number of carbon atoms are preferred. Particularly preferred radicals R are derived from C 12 -C 18 -fatty alcohols, for example coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or C 10 -C 20 oxo alcohols.

AO represents an ethylene oxide (EO) or propylene oxide (PO) moiety, preferably an ethylene oxide moiety. The index n stands for an integer from 1 to 50, preferably from 1 to 20 and especially from 2 to 10. Most preferably, n stands for the numbers 2, 3, 4, 5, 6, 7 or 8. X stands for a monovalent cation or the nth part of an n-valent cation, the alkali metal ions are preferred, and Na ⁺ or K ⁺ including Na, with Na ^{+ being} extremely preferred. Additional cations X ⁺ can be selected from NH ₄ ⁺ ,

Mg ²⁺ , Y ₂ Ca ²⁺ ₂ Mn ²⁺ , and mixtures thereof.

Particularly preferred anionic surfactants are selected from fatty alcohol ether sulfates of the formula A-1

(A-1) with k = 1 1 to 19, n = 2, 3, 4, 5, 6, 7 or 8. Very particularly preferred representatives are Na-Ci2-14 fatty alcohol ether sulfates with 2 EO (k = 1 1-13, n = 2 in Formula A-1).

Also suitable are compounds of the formula R ⁵ -A-SO ^{3 "} Y ⁺ .

In this formula, R ^{5 is} a linear or branched, substituted or unsubstituted alkyl, aryl or alkylaryl radical and the grouping -A- for -O- or a chemical bond. In other words, sulfate (A = O) or sulfonate (A = chemical bond) surfactants can be described by the above formula. Depending on the choice of the group A, certain radicals R ^{5 are} preferred. In the case of the sulfate surfactants (A = O), R ⁵ preferably represents a linear, unsubstituted alkyl radical, more preferably a fatty alcohol radical. Preferred radicals R ⁵ are selected from decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl radicals and mixtures thereof, where the representatives with even number of carbon atoms Atoms are preferred. Particularly preferred radicals R ⁵ are derived from C 12-18 fatty alcohols, for example coconut oil fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or C 10 -C 20 oxo alcohols. Y stands for a monovalent cation or the n-th part of an n-valent cation, the alkali metal ions being preferred, and Na ⁺ or K ⁺ being preferred, Na ^{+ being} extremely preferred. Other cations Y + may be selected from NH ₄ ⁺ , V ₂ Zn ²⁺ , V ₂ Mg ²⁺ , Y ₂ Ca ²⁺ , Y ₂ Mn ²⁺ , and mixtures thereof.

Such particularly preferred anionic surfactants are selected from fatty alcohol sulfates of the formula

with k = 1 1 to 19. Very particularly preferred representatives are Na-Ci2-14 fatty alcohol sulfates (k = 1 1-13).

In the case of the sulfonate surfactants (A = chemical bond) R ⁵ preferably represents a linear or branched unsubstituted alkylaryl radical. Here again, X is a monovalent cation or the nth part of an n-valent cation, the alkali metal ions being preferred, and Na ⁺ or K ⁺ being preferred, Na ^{+ being} extremely preferred. Other cations X ⁺ may be selected from NhV, V ₂ Zn ²⁺ , V ₂ Mg ²⁺ , V ₂ Ca ²⁺ , V ₂ Mn ²⁺ , and mixtures thereof. Such surfactants may be selected from linear or branched alkyl benzene sulfonates. Compounds of alkyl carboxylates may be generally represented by the formula R-COO ^~ X ^+, where R is a straight-chain or branched, saturated or mono- or polyunsaturated Ce-24 alkyl or alkenyl group and may be X ⁺ is selected from the above cations, with the sodium and potassium salts of the alkyl carboxylates being preferred.

Also suitable in the context of the present invention are cationic surfactants. Suitable cationic surfactants are, for example, surface-active, quaternary compounds, in particular having an ammonium, sulfonium, phosphonium, iodonium or arsonium group.

Particularly preferred cationic surfactants are the quaternary, z. T. antimicrobial ammonium compounds (QAV, INCI Quaternary Ammonium Compounds) according to the general formula (R ^I ) (R ") (R '") (R ^IV ) N ⁺ X ^" , in which R ¹ to R ^{IV are} identical or different C i 22-alkyl radicals C 7-28 aralkyl radicals or heterocyclic radicals, where two or, in the case of an aromatic inclusion as in pyridine, even three radicals together with the nitrogen atom form the heterocycle, eg a pyridinium or imidazolinium compound, and X Halide ions, sulfate ions, hydroxide ions or similar anions For optimum antimicrobial action, at least one of the radicals preferably has a chain length of 8 to 18, in particular 12 to 16, carbon atoms.

QACs are by reacting tertiary amines with alkylating agents, such as. As methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also ethylene oxide produced. The alkylation of tertiary amines with a long alkyl radical and two methyl groups is particularly easy; also the quaternization of tertiary amines with two long radicals and one methyl group can be carried out with the aid of methyl chloride under mild conditions. Amines which have three long alkyl radicals or hydroxyl-substituted alkyl radicals are less reactive and are preferably quaternized with dimethyl sulfate.

Suitable QACs are, for example, benzalkonium chloride (N-alkyl-N, N-dimethyl-benzyl

ammonium chloride, CAS No. 8001-54-5), benzalkone B (mp-dichlorobenzyl-dimethyl-C12-alkylammonium chloride, CAS No. 58390-78-6), benzoxonium chloride (benzyl-dodecyl-bis (2-hydroxyethyl) -ammonium chloride) , Cetrimonium bromide (N-hexadecyl-N, N-trimethyl ammonium bromide, CAS No. 57-09-0), benzetonium chloride (N, N-dimethyl-N- [2- [2- [p- (1,1,3,3 - tetramethylbutyl) phenoxy] ethoxy] ethyl] benzylammonium chloride, CAS No. 121-54-0),

Dialkyldimethylammonium chlorides such as di-n-decyldimethylammonium chloride (CAS No. 7173-51-5-5), didecyldimethylammonium bromide (CAS No. 2390-68-3), dioctyldimethylammonium chloride, 1-cetylpyridinium chloride (CAS No. 123-03-5) and thiazoline iodide ( CAS No. 15764-48-1) and mixtures thereof. Preferred QACs are the benzalkonium chlorides with Ce-Cie-alkyl radicals,

in particular C 12-C14-alkylbenzyldimethylammonium chloride. A particularly preferred QAV is Cocospentaethoxymethylammonium methosulfate (INC! PEG-5 Cocomonium Methosutfate;

Rewoquat® CPEM).

To avoid possible incompatibilities of the antimicrobial, cationic surfactants with optionally contained anionic surfactants anionic surfactant compatible and / or as little cationic surfactant as possible or in a particular

Embodiment of the invention completely dispenses with antimicrobial, cationic surfactants.

Also suitable are amphoteric surfactants. Suitable amphoteric surfactants are, for example, betaines of the formula (R) (R ²⁾ (R ³⁾ N ⁺ CH 2 CO ^~ wherein ^R! an optionally interrupted by hetero atoms or hetero atom groups alkyl radical having 8 to 25, preferably 10 to 21 carbon atoms and R ² and R ^{3 are} identical or different alkyl radicals having 1 to 3 carbon atoms, in particular Cic-C22-Alkyldimethylcarboxymethylbetain and C11-O7- Alkylamidopropyldimethylcarboxymethylbetain.

Furthermore, the use of Alkylamidoalkylaminen, alkyl-substituted amino acids, acylated amino acids or biosurfactants as amphoteric surfactants in the context of the present invention is conceivable.

In some embodiments, the at least one compound having an HLB value> 7 is preferably selected from the group of nonionic surfactants, especially from the group of alkyl glycosides and polyalkoxylated fatty alcohols and fatty acid alkyl esters, more preferably from the group of polyalkoxylated fatty alcohols and fatty acid alkyl esters, most preferably the group of polyalkoxylated fatty alcohols as defined above.

In the context of the present invention, especially those compounds with an HLB value> 7 are suitable, which are selected from the group consisting of polyoxyethylene (POE) (4) stearic acid (monoester), POE (4) nonylphenol (ether), POE ( 4) tridecyl alcohol (ether), POE (4) lauryl alcohol (ether), POE (5) sorbitan monooleate, POE (7) lauryl alcohol. POE (40)

Sorbitol hexaoleate, PEG 400 dilaurate, POE (5) nonylphenol (Rather), POE (20) sorbitan tristearate, POP / POE condensates, POE (6) nonylphenol (ether), POE (20) lanolin (ether and ester), POE (20) Sorbitan trioleate, POE (8) stearic acid (monoester), POE (50) sorbitol hexaoleate, POE (6) tridecyl alcohol (ether), PEG 400 monostearate, POE (8) nonylphenol (ether), POE (10)

Stearyl alcohol (ether), POE (8) tridecyl alcohol (ether), POE (8) lauric acid (monoester), POE (10) cetyl alcohol (ether), acetylated POE (10) lanolin, POE (20) glycerol monostearate, PEG 400 monolaurate, POE (16) Lanolin alcohol (ether), POE (4) sorbitan monolaurate, POE (10) nonylphenol (ether), POE (10) octylphenol (ether), PEG 600 monostearate. POE (24) cholesterol, POE (14) Nonylphenol (ether), POE (12) lauryl alcohol, POE (14) lauryl alcohol, POE (20) sorbitan monostearate, POE (20) sorbitan monooleate, acetylated POE (9) lanolin, POE (20) stearyl alcohol. POE (20) oleyl alcohol (ether), PEG 1000 monooleate, POE (20)

Sorbitan monopalmitate, POE (20) cetyl alcohol (ether), POE (25) propylene glycol monostearate, POE (20) nonylphenol (ether), PEG (1000) monolaurate, POE (20) sorbitan monolaurate, POE (23) lauryl alcohol (ether), POE (40 ) Stearic acid (monoester), POE (50) lanolin (ether and ester), POE (25) soyasterol, POE (30) nonylphenol (ether), PEG 4000 distearate, POE (50) stearic acid (monoester), POE (70) dinonylphenol (Ether), POE (20) castor oil (ether, ester).

According to one embodiment, the at least one compound with an HLB value of> 7 is characterized in that it has a melting point in the range of 20 ° C to 80 ° C, in particular 30 ° C to 80 ° C.

According to one embodiment, the at least one compound having an HLB value of> 7 is characterized in that it is homogeneously miscible or emulsifiable with the at least one carrier polymer, in particular with a polyalkylene glycol, preferably with polyethylene glycol (PEG) with a molecular weight of 3,000 to 15,000 is. This ensures a uniform formulation with the main component of the fragrance particles. In certain embodiments, the as described herein is at least one compound having an HLB value of> 7, especially polyethylene glycol having a molecular weight of greater than 1000, preferably having a molecular weight of up to 13,000, more preferably having a molecular weight of up to 12,000, homogeneously miscible and emulsifiable.

If, in the context of this application, "average molecular weight of

 Polyalkylenglykolen "is spoken, then these data in each case refer to the values which arithmetically calculated from the OH number measured in accordance with DIN 53240.

According to one embodiment of the present invention, the at least one compound having an HLB value> 7, as defined herein, in an amount of 0.1 to 30 wt .-%, preferably in an amount of 2 to 25 wt .-%, especially in an amount of 5 to 10% by weight, based on the total weight of the composition. In different

Embodiments, the at least one compound having an HLB value> 7 in an amount of 0.1 to 30 wt .-% in the composition.

The major component of the solid particulate composition as described herein is at least one water-soluble carrier polymer. In different

In embodiments, the at least one water-soluble carrier polymer is characterized by a melting point of> 30 ° C., preferably> 40 ° C. In various embodiments, the at least one carrier polymer is characterized in that it has a melting point of 48 ° C to 300 ° C, preferably from 48 ° C to 120 ° C.

According to the present invention, the at least one carrier polymer is preferably selected from polyalkylene glycols.

In the context of the present invention, those polyalkylene glycols are suitable which have an average molecular weight of> 1000 g / mol, in particular> 1500 g / mol, preferably an average molecular weight of between 3,000 and 13,000, more preferably an average molecular weight of between 3,500 and 12,000, more preferably a having an average molecular weight of between 4,000 and 1,000 and more preferably having an average molecular weight between 6,000 and 8,000. According to the present invention, in particular those polyalkyl glycols are suitable which have a melting point between 40 ° C and 90 ° C, in particular in the range of 45 to 70 ° C. Examples of polyalkylene glycols useful in the context of the present invention are polypropylene glycol and polyethylene glycol.

In some embodiments, the at least one carrier polymer is preferably polyethylene glycol.

In some embodiments, the at least one carrier polymer is a polyethylene glycol having an average molecular weight of> 1500 g / mol, preferably an average molecular weight of between 3,000 and 13,000, more preferably an average

Molecular weight between 3,500 and 12,000, more preferably with a middle one

Molecular weight between 4,000 and 1 1, 000 and particularly preferably with an average molecular weight between 6,000 and 8,000. In some embodiments, such a polyethylene glycol is characterized by a melting point in the range of 45 to 70 ° C, preferably 50 to 65 ° C.

In various embodiments, the at least one carrier polymer is contained in the composition in an amount of from 30 to 95% by weight, preferably from 35 to 85% by weight, for example from 40 to 80 or 40 to 78% by weight, based on the Total weight of

Composition.

Another component of the particulate solid composition as described herein is at least one perfume. A fragrance is an odor-causing chemical substance. In order to stimulate the sense of smell, the chemical substance should be at least partially redistributable in the air, ie the fragrance should at 25 ° C at least in be slightly volatile. If the fragrance is now very volatile, the odor intensity then quickly decreases again. At a lower volatility, the smell impression is more sustainable, ie it does not disappear so quickly. Thus, in one embodiment, the perfume has a melting point ranging from -100 ° C to 100 ° C, preferably from -80 ° C to 80 ° C, more preferably from -20 ° C to 50 ° C, especially from -30 ^' C is up to 20 ° C. In another

In the embodiment, the fragrance has a boiling point ranging from 25 ° C to 400 ° C, preferably from 50 ° C to 380 ° C, more preferably from 75 ° C to 350 ° C, especially from 100 ° C to 330 ° C lies.

Overall, a chemical substance should not exceed a certain molecular weight to act as a fragrance, since too high molecular weight, the required volatility can no longer be ensured. In one embodiment, the fragrance has a molecular weight of 40 to 700 g / mol, more preferably 60 to 400 g / mol.

The smell of a fragrance is perceived by most people as pleasant and often corresponds to the smell of, for example, flowers, fruits, spices, bark, resin, leaves, grasses, mosses and roots. Thus, fragrances can also be used to superimpose unpleasant odors or even to provide a non-smelling substance with a desired odor. As perfumes, individual perfume compounds, e.g. the synthetic products of the ester, ether, aldehyde, ketone, alcohol and type

Hydrocarbons are used.

Fragrance compounds of the aldehyde type are, for example, adoxal (2,6,10-trimethyl-9-undecenal), anisaldehyde (4-methoxybenzaldehyde). Cymal (3- (4-isopropylphenyl) -2-methylpropanal), ethylvanillin, florhydra I (3- (3-isopropylphenyl) butanal), helional (3- (3,4-methylenedioxyphenyl) -2-methylpropanal), heliotropin, hydroxycitronellal , Lauraldehyde, Lyral (3- and 4- (4-hydroxy-4-methylpentyl) -3-cyclohexene-1-carboxaldehyde), methyl nonylacetaldehyde, Lilial (3- (4-tert-butylphenyl) -2-methylpropanal), phenylacetaldehyde , Undecylenaldehyd, vanillin. 2.6.10- Trimethyl-9-undecenal, 3-dodecen-1-al, alpha-n-amyl cinnamic aldehyde, melonal (2,6-dimethyl-5-heptenal), 2,4-dimethyl-3-cyclohexene-1-carboxaldehyde (Triplal ), 4-methoxybenzaldehyde, benzaldehyde, 3- {4-tert-butylphenyl) -propanal, 2-methyl-3- (para-methoxyphenyl) propanal, 2-methyl-4- (2,6,6-timethyl-2 ( 1) -cyclohexen-1-yl) butanal, 3-phenyl-2-propenal, cis- / trans-3,7-dimethyl-2,6-octadiene-1-al, 3,7-dimethyl-6-octene-1 al, [(3,7-dimethyl-6-octenyl) oxy] acetaldehyde, 4-isopropylbenzylaldehyde, 1, 2,3,4, 5,6,7,8-octahydro-8,8-dimethyl-2-naphthaldehyde, 2,4-dimethyl-3-cyclohexene-1-carboxaldehyde, 2-methyl-3- (isopropylphenyl) propanal, 1-decanal, 2,6-dimethyl-5-heptenal, 4- (tricyclo [5.2.1.0 (2, 6)] -decylidene-8) -butanal, octahydro-4,7-methane-1H-indenecarboxaldehyde, 3-ethoxy-4-hydroxybenzaldehyde, para-ethyl-alpha, alpha-dimethylhydrocinnamaldehyde, alpha-methyl-3,4- (methylenedioxy ) -hydrocinnamaldehyde, 3,4- Methyldioxybenzaidehyde, alpha-n-hexyzimtaldehyde, m-cymene-7-carboxaidehyde, aipha-methylphenylacetaldehyde, 7-hydroxy-3,7-dimethyloctanal, undecenal, 2,4,6-trimethyl-3-cyclohexene-1-carboxaldehyde, 4- (3 ) (4-ethyl-3-pentenyl) -3-cyclohexene-carboxaldehyde, 1-dodecanal, 2,4-dimethylcyclo-exen-3-carboxaldehyde, 4- (4-hydroxy-4-methylpentyl) -3-cyclohexene-1-carboxaldehyde, 7-M ethoxy-3,7-dim et hyocta n-1 -ai, 2-methyl undecanal, 2-methyldecanal, 1-nonanal, 1-octanal, 2,6,10-trimethyl-5,9-undecadienal, 2 -Methyl 3- (4-tert-butyl) propanal, dihydrocinnamaldehyde, 1-ethyl-4- (4-methyl-3-pentenyl) -3-cyclohexene-1-carboxaldehyde, 5- or 6-methoxyhexahydro-4,7-methanindane 1- or 2-carboxaldehyde, 3.7-dimethyloctan-1-al, 1-undecanal, 10-undecene-1-al, 4-hydroxy-3-methoxybenzaldehyde, 1-methyl-3- (4-methylpentyl) - 3-cyclohexenecarboxaldehyde, 7-hydroxy-3J-dimethyl-octanal. trans-4-decenal, 2,6-nonadienal, para-tolylacetaldehyde. 4-methylphenylacetaldehyde, 2-methyl-4- (2,6,6-trimethyl-1-cyclohexen-1-yl) -2-butenal, ortho-methoxycinnamaldehyde, 3,5,6-trimethyl-3-cyclohexene-carboxaldehyde, 3J-dimethyl-2-methylene-6-octenal, phenoxyacetaldehyde. 5,9-dimethyl-4,8-decadienal, peonyaldehyde (6.10-dimethyl-3-oxa-5,9-undecadiene-1-al). Hexahydro-4,7-methanindan-1-carboxaldehyde. 2-Methyloctanal. alpha-methyl-4- (1-methylethyl) benzolacetaldehyd. 6,6-dimethyl-2-norpinen-2-propanol aldehyde. para- ethylphenoxyacetaldehyde, 2-methyl-3-phenyl-2-propene-1-al, 3,5,5-trimethylhexanal, hexahydro-8,8-dimethyl-2-naphthaldehyde, 3-propyl-bicyclo- [2.2.1 ] hept-5-en-2-carbaldehyde, 9-decenal, 3-methyl-5-phenyl-1-pentanal, methylnonylacetaldehyde, hexanal and trans-2-hexenal.

For example, ketone-type perfume compounds are methyl-beta-naphthyl ketone, muskindanone (1,2,3,5,6,7-hexahydro-1,1,3,3,3-pentamethyl-4H-inden-4-one), tonyamide (6- Acetyl-1,1,2,4,4,7-hexamethyltetralin), alpha-damascone, beta-damascone, delta-damascone, iso-damascone, damascenone, methylidihydrojasmonate, menthone, carvone, camphor, koavon (3,4,5,6,6-pentamethylhept -3-en-2-one). Fenchone, alpha-ionone, beta-ionone, gamma-methyl-ionone, fiedemono (2-heptylcyclopentanone), dihydrojasmon, cis-jasmone, iso-E-Super (1- (1, 2,3,4,5, 6J, 8-octahydro-2,3,8,8-tetramethyl-2-naphthalenyl) ethane-1-one (and isomers)). Methylcedrenylketon,

Acetophenone, methylacetophenone, para-methoxyacetophenone, methyl-beta-naphthyl ketone, benzylacetone, benzophenone, para-hydroxyphenylbutanone. Celery ketone (3-methyl-5-propyl-2-cyclohexenone), 6-isopropyldecahydro-2-naphthone, dimethyloctenone. Frescomenthe (2-butan-2-yl-cyclohexan-1-one), 4- (1-ethoxyvinyl) -3,3,5,5-tetramethylcyclohexanone. Methyl heptenone, 2- (2- (4-methyl-3-cyclohexen-1-yl) propyl) cyclopentanone, 1- (p-menthene-6 (2) yl) -1-propanone, 4- (4-hydroxy-3 - methoxyphenyl) -2-butanone, 2-acetyl-3,3-dimethylnorbornane, 6,7-dihydro-1,1,2,3,3-pentamethyl-4 (5H) -indanone, 4-damascol, dulcinyl (4 - (1, 3-benzodioxol-5-yl) butan-2-one), hexalone (1- (2,6,6-trimethyl-2-cyclohexene-1-yl) -1, 6-heptadien-3-one ), isocyclone (2-acetonaphthone-1, 2,3,4,5,6,7,8-octahydro-2,3,8,8-tetramethyl), methyl nonyl ketone, methylcyclo- citron, methylene lavender ketone, orivone (4-tert-amylcyclohexanone ), 4-tert-Butylcyclohexanone, Delphon (2-pentyl-cyclopentanone), Muscon (CAS 541-91-3), Neobutenone (1- (5,5-dimethyl-1-cyclohexenyl) pent-4-ene-1 on), Plicaton (CAS 41724-19-0), veioutone (2,2,5-trimethyl-5-pentylcyc! Opentan-1-one), 2,4,4,7-tetramethyl-oct-6-en-3-one and tetrameran (6, 10-dimethylundecene). 2-οη).

Fragrance compounds of the alcohol type are, for example, 10-undecen-1-ol, 2,6-dimethylheptan-2-ol, 2-methylbutanol, 2-methylpentanol, 2-phenoxyethanoi, 2-phenylpropanol, 2-tert-butycyclohexanol, 3,5,5-trimethylcyclohexanol, 3-hexanol, 3-methyl-5-phenyl-pentanol, 3-octanol, 3-phenyl-propanol, 4-heptenol, 4-isopropyl-cyclohexanol, 4-tert-butylcyclohexanol, 6.8 Dimethyl 2-nonanol, 6-nonene-1-ol, 9-decene-1-ol, α-methylbenzyl alcohol, α-terpineol,

Amyl salicylate, benzyl alcohol, benzyl salicylate, β-terpineol, butyl salicylate, citronellol,

Cyclohexyl. Decanol, di-hydromyrcenol. Dimethylbenzylcarbinol, dimethylheptanol, dimethyioctanoi, ethyl salicylate, ethyivaniiin, Eugenoi, Farnesoi, Geranioi, Heptanoi, hexyl salicylate, isoborneol, isoeugenol. Isopulegol, linalool, menthol. Myrtenol, n-hexanol, nerol, nonanol, octanol, p-menthane-7-ol, phenylethyl alcohol, phenol, phenyl salicylate, tetrahydrogeraniol, tetrahydrolinalool, thymol, trans-2-cis-6-nonadicnol, trans-2-noneno-1 ol, trans-2-octenol, undecanol, vanillin, champiniol, hexenol and cinnamyl alcohol.

Fragrance type ester compounds are e.g. Benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinylacetate (DMBCA), phenylethylacetate, benzylacetate, ethylmethylphenylglycinate, allylcyclohexylpropionate, styrallylpropionate,

Benzyl salicylate, cyclohexyl salicylate, floramate, melusate and jasmacycate.

Ethers include, for example, benzyl ethyl ether and ambroxan. To the

Hydrocarbons are mainly terpenes such as limonene and pinene.

Preference is given to using mixtures of different fragrances which together produce an attractive fragrance. Such a mixture of perfumes may also be referred to as perfume or perfume oil. Such perfume oils may also contain natural perfume mixtures as are available from plant sources.

Fragrances of plant origin include essential oils such as angelica root oil, aniseed oil, arnica blossom oil. Basil oil, bay oil, champa blossom oil, citrus oil. Edler fir oil, Edeltann cone oil, elemi oil, eucalyptus oil, fennel oil, pine needle oil, galbanum oil, geranium oil, gingerg ras oil, guaiac wood oil, gurdy balm oil, helichrysum oil, ho oil, ginger oil, iris oil. jasmin oil, cajeput oil,

Calamus oil, chamomile oil, camphor oil, kanga oil, cardamom oil, cassia oil, pine needle oil,

Copaiba balsam, coriander oil, spearmint oil, caraway oil, cumin oil, labdanum oil, lavender oil, lemong rasöl, linden flower oil, lime oil, tangerine oil, balm oil, mint oil, musk oil, muscat oil, myrrh oil, clove oil, neroli oil, niaouli oil, olibanum oil, orange blossom oil,

Orange peel oil, Origanum oil, Palmarosa oil, Patchouli oil, Peruvian balsam oil, Petitgrain oil, Pepper oil, Peppermint oil, Pimentoi, pine oil, rose oil, rosemary oil, ointment, sandalwood oil, celery oil, spiked oil, star aniseed oil, turpentine oil, thuja oil, thymiart oil, verbena oil, vetiver oil, juniper berry oil, wormwood oil, green oil, ylang-ylang oil, hyssop oil, cinnamon oil , Cinnamon leaf oil, lemon oil, lemon oil as well

Cypress oil and ambrettolide, ambroxan, alpha-amylcinnamaldehyde, anethole, anisaldehyde, anisalcohol, anisole, methyl anthranilate, acetophenone, benzylacetone, benzaldehyde, ethyl benzoate. Benzophenone, benzyl alcohol, benzyl acetate, benzyl benzoate,

Benzyl formate, benzyl valerate, borneol, bornyl acetate, Boisambrene forte, alpha-bromostyrene, n-decyl aldehyde, n-dodecyl aldehyde, eugenol, eugenol methyl ether, eucalyptol, farnesol, fenchone, fenchyl acetate, geranyl acetate, geranyl formate, heliotropin, heptincarboxylic acid methyl ester, heptaldehyde, hydroquinone dimethyl ether. Hydroxycinnamaldehyde, Hydroxyzimtalcohol, Indole, Iran. Isoeugenol, isoeugenol methyl ether, isosafrole, jasmon. Camphor, Karvakrol, Karvon, p-cresol methyl ether, coumarin, p-methoxyacetophenone, methyl n-amyl ketone,

Methylanthranilic acid methyl ester, p-ethylacetophenone. Methylchavicol, p-methylquinoline, methyl-beta-naphthyl ketone, methyl-n-nonylacetaldehyde, methyl-n-nonyl ketone, muscone, beta-naphthol ethyl ether, beta-naphthol methyl ether. Nerol, n-nonylaldehyde. Nonyl alcohol. n-octylaldehyde, p-oxyacetophenone, pentadecanolide, beta-phenylethyl alcohol, phenylacetic acid, pulegone, safrole, isoamyl salicylate, methyl salicylate, salicylic acid hexyl ester, cyclohexyl salicylate, santalol, sandelice, skatole, terpineol, thymes, thymol, troenan, gamma undelactone, vanillin, Veratrumaldehyde, cinnamaldehyde, cinnamyl alcohol, cinnamic acid,

Cinnamic acid ethyl ester, cinnamon benzyl ester, diphenyloxide, unions, linalool, linalyl acetate and propionate, melusate, menthol, menthone, methyl-n-heptenone, pinene, phenylacetaldehyde,

Terpinyl acetate, citral, citronellal, and mixtures thereof.

In an alternative embodiment, it may be preferred that at least a portion of the perfume is used as a perfume precursor or in encapsulated form (perfume capsules), especially in microcapsules. The microcapsules may be water-soluble and / or water-insoluble microcapsules. For example, melamine-urea-formaldehyde microcapsules, melamine-formaldehyde microcapsules, urea-formaldehyde microcapsules, or starch microcapsules can be used. "Perfume precursor" refers to compounds that undergo chemical conversion / cleavage, typically by the action of light or other environmental conditions, such as pH, temperature, etc., to release the actual fragrance Such compounds are often referred to as fragrance or "fragrance fragrance".

Regardless of the form in which they are used, the amount of perfume in the composition is preferably between 1 to 20 wt .-%, preferably 1 to 15 wt .-%, in particular from 3 to 10 wt .-%, based on the total weight the composition. In various embodiments, the solid particulate composition as described herein may further comprise at least one fabric conditioning compound. In this context, a textile care compound is understood to mean any compound which gives textile fabrics treated therewith a beneficial effect, such as, for example, a textile softening effect, crease resistance or the harmful or negative effects which result during cleaning and / or conditioning and / or or wearing, such as

Fading, graying, etc., reduced.

The fabric care composition may preferably be made of fabric softening compounds, bleaches, bleach activators, enzymes, silicone oils, anti redeposition agents, optical brighteners, grayness inhibitors, anti-shrinkage agents, wrinkle inhibitors, color transfer inhibitors, antimicrobials, germicides, fungicides, antioxidants, antistatic agents, ironing aids, phobizers and the like Impregnating agents, swelling and slipping agents, UV absorbers and mixtures thereof are selected.

It is particularly preferred that the fabric care compound is a fabric softening compound. It is most preferred that the fabric softening compound is selected from polysiloxanes, fabric softening clays, cationic polymers and mixtures thereof.

The use of polysiloxanes and / or cationic polymers as a fabric care compound in the composition is advantageous because they not only have a softening effect but also enhance the perfume impression on the laundry. The use of softening clays as a textile-care compound in the composition is advantageous because they additionally have a water-softening effect and so for example

Lime deposits on the laundry can be prevented. For optimum performance, it may be preferred for a composition to contain a combination of at least two fabric care compounds.

When the composition according to the invention contains such textile-care compounds, it is used in particular as a textile care agent or softener or as a constituent of such an agent or else as a constituent of a detergent.

Such a fabric conditioner may be in the main wash of an automatic washing or

Cleaning process can be used. For example, the composition may be added to the drum or dispenser compartment of a washing machine along with the detergent or cleaning agent. This has the advantage that no additional rinse is necessary and no unsightly deposits occur in the dispenser Furthermore, such a solid composition in the wash of a

Laundry cleaning process can be used and so the textile-care compound and the perfume already at the beginning of the washing process to transport laundry, so as to be able to develop their full potential. Furthermore, this solid composition is easier and better to handle than liquid compositions, since no drops remain on the edge of the bottle, which lead to subsequent storage of the bottle to edges on the ground or to unsightly deposits in the region of the closure. The same applies in the event that some of the composition is accidentally spilled during dosing. The spilled composition can also be removed easier and cleaner.

A preferably usable polysiloxane has at least the following structural unit

With

 R = independently of one another C 1 -C 30 -alkyl, preferably C 1 -C 4 -alkyl, in particular methyl or ethyl,

n = 1 to 5000, preferably 10 to 2500, in particular 100 to 1500.

It may be preferred that the polysiloxane additionally has the following structural unit:

 R is C 1 -C 30 -alkyl, preferably C 1 -C 4 -alkyl, in particular methyl or ethyl,

 Y = optionally substituted, linear or branched C 1 -C 20 -alkylene, preferably - (CH 2) m - with m = 1 to 16, preferably 1 to 8, in particular 2 to 4, in particular 3,

R ² , R ³ = independently of one another are H or optionally substituted, linear or branched C 1 -C 30 -alkyl, preferably C 1 -C 30 -alkyl which is substituted by amino groups, especially

preferably - (CH 2) b -NH 2 where b = 1 to 10, very preferably b = 2,

x = 1 to 5000, preferably 10 to 2500, in particular 100 to 1500.

If the polysiloxane has only the structural unit a) with R = methyl, then it is a poly-dimethylsiloxane. Polydimethylpolysiloxanes are known as efficient fabric care compounds. Suitable polydimethysiloxanes include DC-200 (ex Dow Corning), Baysilone® M 50,

Baysilone® M 100, Baysilone® M 350, Baysilone® M 500, Baysilone® M 1000, Baysilone® M 1500, Baysilone® M 2000 or Baysilone® M 5000 (all ex GE Bayer Silicones).

However, it may also be preferred that the polysiloxane contains the structural units a) and b). A particularly preferred polysiloxane has the following structure:

(CH ₃ ) 3 Si - [0-Si (CH 3) 2] n - [O-Si (CH ₃ ) {(CH ₂ ) 3 -NH- (CH 2) 2 -NH 2}] x -OSi (CH ₃ ) 3 where the sum n + x is a number between 2 and 10,000.

Suitable polysiloxanes having the structural units a) and b) are for example commercially available under the trade names DC2-8663, DC2-8035, DC2-8203, DC05-7022 or DC2-8566 (all ex Dow Corning). According to the invention are also suitable for example the products commercially available Dow Corning ^® 7224, Dow Corning ^® 929 Cationic Emulsion or Formasil 410 (GE Silicones).

A suitable fabric softening clay is, for example, a smectite clay. Preferred smectite clays are beidellite clays, hectorite clays, laponite clays, montmorillonite clays, nontronite clays, saponite clays, sauconite clays, and mixtures thereof. Montmorillonite clays are the preferred softening clays. Bentonites contain mainly montmorillonites and can serve as a preferred source of fabric softening clay. The bentonites can be used as powder or crystals.

Suitable bentonites are sold, for example, under the names Laundrosil® by Süd-Chemie or under the name Detercal by Laviosa. It is preferred that the textile care composition contains a powdered bentonite as a fabric care compound.

Suitable cationic polymers include, in particular, those described in "CTFA International Cosmetic Ingredient Dictionary", Fourth Edition, J.M. Nikitakis, et al., Editors, published by the Cosmetic, Toiletry, and Fragrance Association, 1991, and US Pat

The following is a list of some suitable Polyquaternium compounds.

POLYQUATERNIUM-1 (CAS number: 68518-54-7)

Definition: {(HOCH2CH2) 3N ⁺ -CH 2 CH = CHCH 2 [N ⁺ (CH ₃₎ 2 CH 2 CH = CHCH 2] xN ⁺ (CH2CH20H) _3} [Cr] ₊ 2 x POLYQUATERNIUM-2 (CAS number: 63451-27-4)

Definition: [-N (CH _{3) 2} -CH 2 CH ₂ CH 2 -NH-C (0) -NH-CH ₂ CH ₂ CH 2 N (CH ₃₎ 2-CH2CH20CH2CH2-] ²⁺ (Cl ^") ₂

Polyquaternium-3

 Definition: Copolymer of acrylamide and trimethylammoniumethylmethacrylate methosulphate POLYQUATERNIUM-4 (CAS Number: 92183-41 -0)

 Definition: Copolymer of hydroxyethylcellulose and diallyldimethylammonium chloride

For example, available as Celquat® H 100 or Celquat® L200 (ex National Starch)

POLYQUATERNIUM-5 (CAS number: 26006-22-4)

 Definition: Copolymer of acrylamide and β-methacrylyloxyethyltrimethylammonium methosulfate.

POLYQUATERNIUM-6 (CAS number: 26062-79-3)

Definition: Polymer of dimethyldiallylammonium chloride

POLYQUATERNIUM-7 (CAS number: 26590-05-6)

 Definition: Polymeric quaternary ammonium salt consisting of acrylamide and

Dimethyldiallylammonium chloride monomers.

Polyquaternium-8

 Definition: Polymeric quaternary ammonium salt of methyl and stearyldimethylaminoethyl methacrylate, which was quaternized with dimethyl sulfate

Polyquaternium-9

 Definition: Polymeric quaternary ammonium salt of polydimethylaminoethyl methacrylate quaternized with methyl bromide

POLYQUATERNIUM-10 (CAS number: 68610-92-4)

Definition: Quaternized hydroxyethylcellulose

POLYQUATERNIUM-1 1 (CAS number: 53633-54-8)

 Definition: Quaternary ammonium polymer formed by reaction of diethyl sulfate with the copolymer of vinylpyrrolidone and dimethylaminoethyl methacrylate.

POLYQUATERNIUM-12 (CAS number: 68877-50-9) Definition: Quaternary ammonium polymer salt obtainable by reaction of the ethyl methacrylate / -abietyl methacrylate / diethylaminoethyl methacrylate copolymer with dimethyl sulfate

POLYQUATERNIUM-13 (CAS number: 68877-47-4)

 Definition: Polymeric quaternary ammonium salt obtained by reaction of the

Ethyl methacrylate / oleyl methacrylate / diethylaminoethyl methacrylate copolymer with dimethyl sulfate is available

POLYQUATERNIUM-14 (CAS number: 27103-90-8)

Definition: Polymeric quaternary ammonium salt of the formula - {- CH ₂ -C- (CH ₃ ) - [C (O) O-CH ₂ CH ₂ -N (CH ₃ ) ₃ 1} x ⁺ [CH ₃ SO ₄ ] -x

POLYQUATERNIUM-15 (CAS number: 35429-19-7)

 Definition: Copolymer of acrylamide and β-methacrylyloxyethyltrimethylammonium chloride POLYQUATERNIUM-16 (CAS number: 95144-24-4)

 Definition: Polymeric quaternary ammonium salt formed from methylvinylimidazolium chloride and vinylpyrrolidone

POLYQUATERNIUM-17 (CAS number: 90624-75-2)

 Definition: Polymeric quaternary ammonium salt obtainable by reaction of adipic acid and dimethylaminopropylamine with dichloroethyl ether.

Polyquaternium-18

 Definition: Polymeric quaternary ammonium salt, which is obtainable by reaction of azelaic acid and dimethylaminopropylamine with dichloroethyl ether.

Polyquaternium-19

 Definition: Polymeric quaternary ammonium salt, which is obtainable by reaction of polyvinyl alcohol with 2,3-epoxypropylamine.

Polyquaternium-20

 Definition: Polymeric quaternary ammonium salt obtainable by reaction of polyvinyl octadecyl ether with 2,3-epoxypropylamine.

POLYQUATERNIUM-21 (CAS number: 102523-94-4)

Definition: polysiloxane / polydimethyldialkylammonium acetate copolymer POLYQUATERNIUM-22 (CAS number: 53694-17-0)

 Definition: dimethyldiallylammonium chloride / acrylic acid copolymer

POLYQUATERNIUM-24 (CAS number: 107987-23-5)

 Definition: Polymeric quaternary ammonium salt from the reaction of hydroxyethylcellulose with a lauryldimethylammonium substituted epoxide

Polyquaternium-27

 Definition: Block copolymer from the reaction of Polyquaternium-2 with Polyquaternium-17. POLYQUATERNIUM-28 (CAS number: 131954-48-8)

 Definition: vinylpyrrolidone / methacrylamidopropyltrimethylammonium chloride copolymer POLYQUATERNIUM-29

 Definition: Chitosan, which was reacted with propylene oxide and quaternized with epichlorohydrin

Polyquaternium-30

Definition: Polymeric quaternary ammonium salt of the formula: - [CH 2 C (CH 3) (C (O) OCH 3)] x- [CH ₂ C (CH 3) (C (O) OCH ₂ CH ₂ N ⁺ (CH 3) ₂ CH ₂ COO-)] _y -

POLYQUATERNIUM-31 (CAS number: 136505-02-7)

POLYQUATERNIUM-32 (CAS number: 35429-19-7)

 Definition: Polymer of N, N, N-trimethyl-2 - [(2-methyl-1-oxo-2-propenyl) oxy] -ethanaminium chloride with 2-propenamide

POLYQUATERNIUM-37 (CAS number: 26161-33-1)

Definition: homopolymer of methacryloyltrimethyl chloride

For example, available as Synthalen® CR (ex 3V Sigma)

POLYQUATERNIUM-44 (CAS number: 150595-70-5)

 Definition: Quaternary ammonium salt of the copolymer of vinylpyrrolidone and quaternized imidazoline

POLYQUATERNIUM-68 (CAS-Number: 827346-45-2)

Definition: Quaternized copolymer of vinylpyrrolidone, methacrylamide, vinylimidazole and quaternized vinylimidazole It may be preferred that the composition contains a fabric softening compound and one or more other fabric care compounds.

The amount of fabric care compound in the composition may, in various embodiments, be 0.1 to 15 weight percent and preferably between 2 and 12 weight percent.

The composition may optionally contain other ingredients. To the

may improve performance and / or aesthetic properties of the composition, regardless of its purpose, these may contain additional ingredients, preferably selected from the group consisting of dyes, fillers, pearlescing agents, skin-care compounds, bittering agents and mixtures thereof.

In order to improve the aesthetic impression of the composition, it can be dyed with suitable dyes. Preferred dyes, the selection of which presents no difficulty to the skilled person, should have a high storage stability and insensitivity to the other ingredients of detergents or cleaning agents and to light and no pronounced substantivity to textile fibers so as not to stain them.

Furthermore, the composition may contain a filler such as silica. The amount of filler may be between 0, 1 and 10 wt .-% and is preferably 1 to 5 wt .-%.

The composition may also contain a pearlescing agent to increase gloss.

Examples of suitable pearlescing agents are ethylene glycol mono- and distearate and PEG-3-distearate.

Furthermore, the composition may comprise a skin care compound.

A skin care compound is a compound or mixture of

Compounds understood, which attract on contact of a textile with the detergent on the textile and on contact of the textile skin with the skin confer an advantage compared to a textile which has not been treated with the composition of the invention. This benefit may include, for example, the transfer of the skin care compound from the textile to the skin, less water transfer from the skin to the textile, or less friction on the skin surface through the textile. The skin care composition is preferably hydrophobic, may be liquid or solid, and must be compatible with the other ingredients of the solid, fabric care composition. For example, the skin care compound

a) waxes such as carnauba, spermaceti, beeswax, lanolin, derivatives thereof and mixtures thereof;

b) Plant extracts, for example vegetable oils such as avocado oil, olive oil, palm oil, palm kernel oil, rapeseed oil, linseed oil, soybean oil, peanut oil, coriander oil, castor oil, poppy seed oil, cocoa oil, coconut oil, pumpkin seed oil, wheat germ oil, sesame oil, sunflower oil, almond oil, macadamia nut oil, apricot kernel oil, hazelnut oil , Jojoba oil or canola oil, chamomile, aloe vera and mixtures thereof;

c) higher fatty acids such as lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, linoleic acid, linolenic acid, isostearic acid or polyunsaturated fatty acids; d) higher fatty alcohols, such as lauryl alcohol, cetyl alcohol, stearyl alcohol, oleyl alcohol,

 Behenyl alcohol or 2-hexadecanol,

e) esters such as cetyloctanoate, lauryl lactate, myristyl lactate, cetyl lactate, isopropyl myristate,

 Myristyl myristate, isopropyl palmitate, isopropyl adipate, butyl stearate, decyl oleate,

 Cholesterol isostearate, glycerol monostearate, glyceryl distearate, glycerol tristearate, alkyl lactate, alkyl citrate or alkyl tartrate;

f) hydrocarbons such as paraffins, mineral oils, squalane or squalene;

g) lipids;

h) vitamins such as vitamins A, C or E or vitamin alkyl esters;

i) phospholipids;

j) sunscreens such as octyl methoxyl cinnamate and butyl methoxybenzoyl methane;

k) silicone oils such as linear or cyclic polydimethylsiloxanes, amino-, alkyl-, alkylaryl- or aryl-substituted silicone oils and

I) mixtures thereof

include.

The amount of skin-care compound is preferably between 0.01 and 10% by weight, preferably between 0.1 and 5% by weight and most preferably between 0.3 and 3% by weight, based on the solid composition. It may be that the skin-nourishing compound additionally has a textile care effect.

To prevent oral ingestion of the composition by humans, particularly children, or animals, it may contain a bittering agent such as Bitrex®.

The particles of the composition as described herein are, in particular, substantially spherical, figurative, scale, cuboid, cylindrical, conical or needle-shaped Particle. For example, the particles may have a gummy-like, figurative design. Their maximum extent in a spatial dimension is preferably from 0.5 to 10 mm, in particular 0.8 to 7 mm and particularly preferably 1 to 3 mm. This means that, for example in the case of spherical particles, the diameter of the particles is from 0.5 to 10 mm, in particular 0.8 to 7 mm and particularly preferably 1 to 3 mm. Usually, the weight of the individual particles is between 2 and 150 mg, preferably between 5 and 10 mg.

The invention also relates to a process for the preparation of a solid composition as defined herein in which the water-soluble carrier polymer is melted, optionally in the molten state with the at least one perfume comprising at least one compound having an HLB value of> 7 and optionally with other, for example, as defined above components is mixed. Methods of forming the particles as described herein differ depending on the desired shape of the particles. Suitable methods are known in the art. The mixture with the at least one perfume and the at least one compound with an HLB value of> 7 and / or optionally contained further constituents can also take place in various embodiments before melting of the carrier polymer. Then, in the step of melting, the mixture is melted directly.

In various embodiments, the melting is carried out by heating to a

Temperature not more than 20 ° C above the melting point of the carrier polymer.

The solid, particulate composition, the particles of which, as described herein, are characterized by accelerated solubility in an aqueous solution may be part of a fabric treatment agent. The advantage of the particles stabilized as described herein is that complete solubility can be achieved at both low water temperatures and short wash cycles. Thus, particle residues after completion of a washing process can be significantly reduced or even completely avoided.

The invention therefore also relates to the use of the solid composition as described herein as a fabric care agent, preferably fragrance and / or softener, for fragrancing and / or conditioning textile fabrics. The composition may be a textile treatment agent such as, for example, a fabric softener or a part of such an agent.

Furthermore, the invention relates to a washing or cleaning agent comprising a solid, particulate composition according to the invention. By introducing the solid, particulate composition according to the invention into a washing or cleaning agent, the consumer is provided with a textile care washing or cleaning composition

Detergent ("2in1" washing or cleaning agent) available and he does not need to dose two agents as well as no separate rinse

Perfumed composition, does not need to be perfumed also the detergent or cleaning agent. Not only does this result in lower costs, it is also beneficial for consumers with sensitive skin and / or allergies.

The composition described herein is particularly suitable for conditioning fabrics and, together with a conventional washing or cleaning agent, is brought into contact with the textile fabrics in the (main) wash cycle of a conventional washing and cleaning process.

If the composition according to the invention is part of a washing or cleaning agent, a solid washing or cleaning agent may preferably be mixed with from 1 to 20% by weight, in particular from 5 to 15% by weight, of the composition according to the invention.

The textile-care washing or cleaning compositions according to the invention contain surfactant (s) in addition to the composition according to the invention, it being possible to use anionic, nonionic, zwitterionic and / or amphoteric surfactants. Preference is given to

From an application point of view mixtures of anionic and nonionic surfactants. The total surfactant content of a detergent is preferably below 40% by weight, and more preferably below 35% by weight, based on the total liquid detergent. Suitable surfactants are readily known to those skilled in the art.

In addition to the composition according to the invention and the surfactants, the detergents or cleaning agents may contain further ingredients which further improve the performance and / or aesthetic properties of the washing or cleaning agent. In the context of the present invention, preferred washing or cleaning agents additionally comprise one or more substances from the group of builders, bleaches, bleach activators, enzymes, perfumes, perfume carriers, fluorescers, dyes, foam inhibitors, silicone oils, antiredeposition agents, optical brighteners, grayness inhibitors, anti-shrinkage agents, anti-crease agents .

Color transfer inhibitors, antimicrobial agents, germicides, fungicides, antioxidants, preservatives, corrosion inhibitors, antistatic agents, bittering agents, ironing aids, repellents and impregnating agents, swelling and anti-slip agents, neutral filler salts and UV absorbers. Suitable builders which may be present in the detergents or cleaners are in particular silicates, aluminum silicates (in particular zeolites), carbonates, salts of organic di- and polycarboxylic acids and mixtures of these substances.

Organic builders that may be present in the detergent or cleaning agent include polycarboxylate polymers such as polyacrylates and acrylic acid / maleic acid copolymers, polyaspartates and monomeric polycarboxylates such as citrates, gluconates, succinates or malonates, which are preferably used as sodium salts.

Among the compounds serving as bleaches in water H2O2, sodium perborate tetrahydrate and sodium perborate monohydrate are of particular importance. Further useful bleaching agents are, for example, sodium percarbonate, peroxypyrophosphates,

Citrate perhydrates and H2O2-yielding peracidic salts or peracids, such as perbenzoates,

Peroxophthalates, diperazelaic acid, phthaloiminoperacid or diperdodecanedioic acid.

In order to achieve an improved bleaching effect when washing at temperatures of 60 ° C and below, bleach activators can be incorporated into the detergents or cleaners. As bleach activators, compounds which are aliphatic under perhydrolysis conditions

Peroxycarboxylic acids having preferably 1 to 10 carbon atoms, in particular 2 to 4 carbon atoms, and / or optionally substituted perbenzoic acid, can be used. 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-nonanoyl or isononanoyloxybenzenesulfonate (n- or iso-NOBS), carboxylic anhydrides, in particular phthalic anhydride, acylated polyhydric alcohols, in particular triacetin, ethylene glycol diacetate and 2,5-diacetoxy-2,5-dihydrofuran.

In addition to or in place of the conventional bleach activators, so-called bleach catalysts can also be incorporated into the detergents or cleaners. These substances are bleach-enhancing transition metal salts or

Transition metal complexes such as Mn, Fe, Co, Ru or Mo saline complexes or - carbonyl complexes. Mn, Fe, Co, Ru, Mo, Ti, V and Cu complexes with nitrogen-containing tripod ligands and Co, Fe, Cu and Ru ammine complexes can also be used as bleach catalysts. The washing or cleaning agent may contain enzymes in encapsulated form and / or directly in the washing or cleaning agent. Suitable enzymes include in particular those from the classes of hydrolases such as proteases, esterases, lipases or lipolytic enzymes, amylases, cellulases or other glycosyl hydrolases, hemicellulases, cutinases, β-glucanases, oxidases, peroxidases, mannanases, perhydrolases and / or laccases and mixtures of said enzymes in question. Particularly suitable are bacterial strains or fungi such as Bacillus subtilis, Bacillus licheniformis, Streptomyceus griseus and Humicola insolens derived enzymatic agents. 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 acting Enzymes and cellulase, but in particular protease and / or lipase-containing mixtures or

Mixtures with lipolytic enzymes are of particular interest. Examples of such lipolytic enzymes are the known cutinases. Peroxidases or oxidases have also proved suitable in some cases. Suitable amylases include in particular α-amylases, iso-amylases, pullulanases and pectinases. As cellulases are preferably cellobiohydrolases, endoglucanases and ß-glucosidases, which are also called cellobiases, or mixtures thereof used. Since different cellulase types differ by their CMCase and avicelase activities, the desired activities can be set by targeted mixtures of the cellulases.

The enzymes may be adsorbed to carriers to protect against premature degradation. The proportion of enzymes or enzyme granules directly in the wash or

Detergent may for example be about 0.01 to 5 wt .-%, preferably 0, 12 to about 2.5 wt .-%.

It may, for example, in special detergents or cleaners for consumers with allergies and / or sensitive skin, but also be preferred that the washing or

Detergent contains no enzymes.

In one embodiment, the washing or cleaning agent optionally contains one or more fragrances in an amount of usually up to 10 wt .-%, preferably 0.5 to 7 wt .-%, in particular 1 to 3 wt .-%. The amount of fragrance used is also dependent on the type of detergent or cleaning agent. However, it is particularly preferred that the perfume is introduced into the detergent or cleaning agent via the composition described herein. However, it is also possible for the washing or cleaning agent to contain fragrances which are not introduced into the washing or cleaning agent via the composition. In order to improve the aesthetic impression of the detergents or cleaners, they may (optionally only partially) be colored with suitable dyes. Preferred dyes, the selection of which presents no difficulty to the skilled person, have a high storage stability and insensitivity to the other ingredients of detergents or cleaning agents and to light and no pronounced substantivity to textile fibers so as not to stain them.

Suitable foam inhibitors which can be used in the detergents or cleaners are, for example, soaps, paraffins or silicone oils, which may optionally be applied to support materials.

Suitable soil release polymers, also referred to as "anti-redeposition agents", include, for example, nonionic cellulose ethers such as methyl cellulose and methyl hydroxypropyl cellulose having a methoxy group content of 15 to 30 wt% and hydroxypropyl groups of 1 to 15 wt%, respectively based on the nonionic cellulose ether and the known from the prior art polymers of phthalic acid and / or terephthalic acid or derivatives thereof, in particular polymers of ethylene terephthalates and / or polyethylene and / or polypropylene glycol terephthalates or anionic and / or nonionic modified derivatives thereof. Suitable derivatives include the sulfonated derivatives of phthalic acid and

Terephthalic acid polymers. Another class of suitable soil-release polymers, in particular for cotton-containing textiles, are modified, for example alkoxylated and / or quaternized and / or oxidized, polyamines. The polyamines are, for example, polyalkyleneamines, such as polyethyleneamines, or polyalkylenimines, such as polyethylenimines. Preferred examples of this class of soil release polymers are ethoxylated polyethylenimines and ethoxylated polyethyleneamines.

Optical brighteners (so-called "whiteners") can be added to laundry detergents or cleaners to eliminate graying and yellowing of the treated fabrics, which will attract the fiber and cause lightening and fake bleaching by exposing invisible ultraviolet radiation to visible . convert longer wavelength light, the absorbed from sunlight ultraviolet light is radiated as a pale blue fluorescence and the yellow shade of the grayed or yellowed laundry to yield pure white Suitable compounds originate for example from the substance classes of the 4,4 ^'- diamino-2,2 ^{stilbenedisulfonic} acids (flavonic), ^{4,4'-biphenylene} -Distyryl, Methylumbelliferone, coumarins, dihydroquinolinones, 1, 3-diaryl pyrazolines, naphthalimides, benzoxazole,

Benzisoxazole and benzimidazole systems and those substituted by heterocycles Pyrene derivatives. The optical brighteners are usually used in amounts of between 0% and 0.3% by weight, based on the finished washing or cleaning agent.

Grayness inhibitors have the task of keeping the dirt detached from the fiber suspended in the liquor and thus preventing the dirt from being rebuilt. Water-soluble colloids of mostly organic nature are suitable for this purpose, for example glue, gelatine, salts of ether sulfonic acids or cellulose or salts of acidic sulfuric acid esters of cellulose or starch. Also, water-soluble polyamides containing acidic groups are suitable for this purpose. Furthermore, soluble starch preparations and other than the above-mentioned starch products can be used, for example degraded starch, aldehyde starches, etc. Polyvinylpyrrolidone is also useful. However, preference is given to cellulose ethers such as

Carboxymethylcellulose (Na salt), methylcellulose, hydroxyalkylcellulose and mixed ethers such as methylhydroxyethylcellulose, methylhydroxypropylcellulose, methylcarboxymethylcellulose and mixtures thereof in amounts of from 0.1 to 5 wt .-%, based on the detergents or cleaning agents used.

In order to effectively suppress dye release and / or dye transfer to other fabrics during washing and / or cleaning of dyed fabrics, the laundry detergent or cleaning agent may contain a color transfer inhibitor. It is preferred that the dye transfer inhibitor is a polymer or copolymer of cyclic amines. When

Color transfer inhibiting polymers include polyvinylpyrrolidone (PVP),

Polyvinylimidazole (PVI), copolymers of vinylpyrrolidone and vinylimidazole (PVP / PVI),

Polyvinylpyridine N-oxide, poly-N-carboxymethyl-4-vinylpyridium chloride and mixtures thereof.

The amount of dye transfer inhibitor based on the total amount of the detergent or cleaning agent is preferably from 0.01 to 2 wt .-%, preferably from 0.05 to 1 wt .-% and more preferably from 0, 1 to 0.5 wt. -%.

Alternatively, however, enzymatic systems comprising a peroxidase and

Hydrogen peroxide or a hydrogen peroxide in water-yielding substance, are used as a color transfer inhibitor. The addition of a mediator compound for the peroxidase, for example an acetosyringone, a phenol derivative or a phenotiazine or phenoxazine, is preferred in this case, wherein additionally the above-mentioned polymeric dye transfer inhibitors can be used.

Since textile fabrics, in particular of rayon, rayon, cotton and their mixtures, can tend to wrinkle, because the individual fibers are sensitive to bending, buckling, pressing and squeezing transversely to the fiber direction, the detergents or cleaners contain synthetic crease inhibitor. These include, for example, synthetic products based on fatty acids, fatty acid esters, fatty acid amides, alkylol esters, -alkylolamides or fatty alcohols, which are usually reacted with ethylene oxide, or products based on lecithin or modified phosphoric acid ester.

To combat microorganisms washing or cleaning agents may contain antimicrobial agents. Here one differentiates depending on the antimicrobial spectrum and

Mechanism of action between bacteriostats and bactericides, fungistats and fungicides etc. Important substances from these groups are, for example, benzalkonium chlorides,

Alkylarylsulfonate, halophenols and Phenolmercuriacetat, which can be completely dispensed with in the inventive detergents or cleaning agents on these compounds.

The detergents or cleaners according to the invention may contain preservatives, it being preferred to use only those which have no or only a slight amount

possess skin-sensitizing potential. Examples are sorbic acid and its salts,

Benzoic acid and its salts, salicylic acid and its salts, phenoxyethanol, 3-iodo-2-propynyl butylcarbamate, sodium N- (hydroxymethyl) glycinate, biphenyl-2-ol and mixtures thereof. A suitable preservative is the solvent-free, aqueous combination of diazolidinyl urea, sodium benzoate and potassium sorbate (available as Euxyl® K 500 ex Schuelke & Mayr), which can be used in a pH range up to 7.

To unwanted, caused by oxygen and other oxidative processes changes to the washing or cleaning agent and / or the treated textile

To prevent fabrics, the detergents or cleaning agents may contain antioxidants. This class of compounds includes, for example, substituted phenols,

Hydroquinones, catechols and aromatic amines as well as organic sulfides, polysulfides, dithiocarbamates, phosphites, phosphonates and vitamin E.

Increased comfort may result from the additional use of antistatic agents added to the detergents or cleaners. The most surface-active antistatic agents can be subdivided into nitrogen-containing (amines, amides, quaternary ammonium compounds), phosphorus-containing (phosphoric acid esters) and sulfur-containing (alkyl sulfonates, alkyl sulfates) antistatic agents.

To improve the rewettability of the treated fabrics and to facilitate the ironing of the treated fabrics, for example, silicone derivatives can be used in the detergents or cleaners. These additionally improve the rinsing out of the washing or cleaning agents by their foam-inhibiting

Properties. Finally, the detergents or cleaning agents may also contain UV absorbers. Suitable compounds include benzophenone having substituents in the 2- and / or 4-position or substituted benzotriazoles.

In order to avoid the catalyzed by heavy metals decomposition of certain detergent ingredients, substances that complex heavy metals can be used. Examples of suitable heavy metal complexing agents are the alkali metal salts of ethylenediaminetetraacetic acid (EDTA) or nitrilotriacetic acid (NTA) and alkali metal salts of anionic salts

Polyelectrolytes such as polymaleates and polysulfonates. A preferred class of

Complexing agents are the phosphonates. These 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) and 2-phosphonobutane-1,2,4-tricarboxylic acid ( PBS-AM), which are mostly used in the form of their ammonium or alkali metal salts.

In addition, neutral fillers such as sodium sulfate or sodium carbonate may be included in the solid detergents or cleaners.

The washing or cleaning agents according to the invention can be used in particular for cleaning and conditioning textile fabrics.

For the preparation of the washing or cleaning agents according to the invention, the washing or cleaning agent without the composition of the invention is first prepared by known processes, which include, for example, drying steps, mixing steps, densification steps,

The product obtained may then be mixed with the solid, particulate composition

Detergent tablets may follow the mixing step with further compaction and / or shaping steps.

Finally, the invention also relates to the use of such washing or cleaning agents for washing textiles or cleaning solid surfaces or methods for cleaning textiles or hard surfaces, wherein in at least one method step, a washing or cleaning agent as described herein is used. The preferred embodiments described in connection with the compositions of the invention are transferable to the detergents and cleaners as well as the uses and methods described herein, and vice versa.

Examples

The solubility of lozenges of different composition in an aqueous solution was compared. For this purpose, the weighed-up mixtures were melted with stirring and then dropped using a pipette onto a metal plate. The initial weight for the solubility test was 10 g each. The lozenges thus produced were then added to 32 ° C tempered water and dissolved with stirring.

Pastilles 1:

 30 parts by weight PEG 3400, 70 parts by weight PEG 6000. Pastilles 2:

 28.5% parts by weight PEG 3400, 66.5% parts by weight PEG 6000, 5% by weight Dehydol LT 7 (BASF), i. C12-C18 fatty alcohol + 7EO

Results of the solubility test:

 In a simultaneous comparison in two beakers (identical stirring arrangement and stirring conditions) the type 2 pastilles were dissolved about 2 minutes faster.

Claims

claims

1. Solid, particulate composition comprising at least one water-soluble

 Carrier polymer having a melting point> 30 ° C, preferably> 40 ° C, preferably selected from polyalkylene glycols, more preferably polyethylene glycol, and at least one perfume, characterized in that the composition comprises at least one compound with an HLB value of> 7 selected from the group consisting of nonionic surfactants, anionic surfactants, cationic surfactants and amphoteric surfactants for accelerating the solubility of the composition in an aqueous solution.

2. The composition according to claim 1, characterized in that the at least one compound having an HLB value of> 7

 (A) is homogeneously miscible or emulsifiable with polyethylene glycol having a molecular weight of 3,000 to 15,000; and or

 (B) has a melting point in the range of 20 ° C to 80 ° C; and or

 (C) is selected from the group of nonionic surfactants, in particular from the group of alkyl glycosides and polyalkoxylated fatty alcohols and fatty acid alkyl esters, more preferably from the group of polyalkoxylated fatty alcohols and fatty acid alkyl esters, most preferably from the group of polyalkoxylated fatty alcohols; and or

 (D) is contained in an amount of 0.1 to 30% by weight in the solid composition.

3. Composition according to claim 1 or 2, characterized in that the

 water-soluble carrier polymer

 (A) has a melting point of 48 ° C to 300 ° C, preferably from 48 ° C to 120 ° C; and or

 (B) is contained in an amount of 30 to 95 wt .-%; and or

 (C) a polyethylene glycol having an average molecular weight of> 1500 g / mol, preferably having an average molecular weight of from 3,000 to 13,000, more preferably having an average molecular weight of from 3,500 to 12,000, even more preferably having an average molecular weight of from 4,000 to 10,000, and most preferably having one average molecular weight between 6,000 and 8,000 and a melting point in the range of 45 to 70 ° C, preferably 50 to 65 ° C.

4. Composition according to one of claims 1 to 3, characterized in that the at least one perfume

 (A) is contained in an amount of 0.1 to 20% by weight in the composition; and or

(B) is used in the form of perfume capsules and / or perfume oils.

Composition according to any one of Claims 1 to 4, characterized in that the composition also comprises at least one textile care compound, preferably selected from textile softening compounds,

 Silicone oils, anti-redeposition agents, optical brighteners, grayness inhibitors, anti-shrinkage agents, anti-wrinkling agents, color transfer inhibitors, antimicrobial agents, germicides, fungicides, antioxidants, antistatic agents, ironing auxiliaries, repellents and impregnating agents, swelling and anti-slip agents, UV absorbers and mixtures thereof.

Composition according to any one of Claims 1 to 5, characterized in that the textile care compound is a fabric softening compound, preferably selected from polysiloxanes, textile softening clays, cationic polymers and mixtures thereof.

7. A composition according to any one of claims 1 to 6, characterized in that the composition contains additional ingredients, preferably selected from the group consisting of dyes, fillers, pearlescing agents, skin care

 Compounds, bitter substances and mixtures thereof.

8. Composition according to one of claims 1 to 7, characterized in that the particles are substantially spherical, figurative, scale, cuboid, cylindrical, conical or needle-shaped particles, wherein the maximum extent in a spatial dimension preferably in the range from 0.5 to 10 mm, in particular 0.8 to 7 mm and particularly preferably 1 to 3 mm.

9. Use of the solid composition according to any one of claims 1 to 8 as

 Fabric care products, preferably fragrancing and / or softener, for scenting and / or conditioning textile fabrics.

10. A washing or cleaning composition comprising a solid composition according to any one of claims 1 to 7.