EP3360951A1 - Composition comprising perfumed oil and encapsulated perfumes - Google Patents

Abstract

The present invention relates to a composition in the form of a suspension comprising at least one free perfume oil, at least one encapsulated perfume oil and at least one specific stabilizer according to formula I. Furthermore, the present invention is directed to a process for preparing such a composition and to the use of those described herein Stabilizers for stabilizing a composition containing both a perfume oil and perfume capsules. Furthermore, the present invention also relates to an agent, such as cosmetic products, detergents or cleaners, containing at least one composition as described herein.

Description

The present invention relates to a composition in the form of a suspension comprising at least one free perfume oil, at least one encapsulated perfume oil and at least one specific stabilizer. Further, the present invention is directed to a process for making such a composition and to the use of the stabilizers described herein for stabilizing a composition containing both perfume oil and perfume capsules. Furthermore, the present invention also relates to an agent, such as cosmetic products, detergents or cleaners, containing at least one composition as described herein.

The commonly used detergents and cleaners as well as cosmetics are usually perfumed. In addition to the actual perfuming by the free fragrances, for example in the form of perfume oils, increasingly encapsulated perfumes are used. On the part of the consumers, a sufficient own scenting of the product as well as a covering of "bad" secondary scents is desired. Furthermore, long-lasting and fresh perfumes are desired. Such properties can be achieved in an advantageous manner by the use of encapsulated fragrances.

In the production of corresponding products, the perfume oil is currently dosed directly into the corresponding product formulations or sprayed on powdery products. The latter inevitably leads to undesirable losses. Before and during the dosing of encapsulated perfumes (capsule slurries), it is necessary to thoroughly homogenize them to ensure a homogeneous and qualitatively appropriate dosage. This process step is not particularly economical due to the high expenditure of time. In addition, two metering operations with two separate metering units are required for the metering of the perfume oil and the encapsulated perfuming. Again, the economic aspect is not optimal due to the longer production times and investments in metering units. In addition, very small amounts (<0.05%) of encapsulated perfumes can currently only be dosed with a high error.

The object of the present invention was therefore to provide a stable combination of perfume oils and encapsulated perfumes (capsule slurries) in order to realize a simple and efficient dosing of the described components.

It has now been found that this object is achieved by the addition of at least one stabilizer selected from the group of alk (en) ylsulfosuccinamates according to formula I, where R = C ₈ -C ₁₈ -alkyl, C ₈ -C ₁₈ -alkenyl and M ⁺ = Na ⁺ , K ⁺ , NH ₄ ⁺ , to a mixture containing both perfume oil and perfume capsules, can be dissolved.

In a first aspect, the present invention is therefore directed to a composition, characterized in that the composition comprises at least one free perfume oil, at least one encapsulated perfume oil and at least one stabilizer selected from the group according to formula I. The composition is in the form of a stable suspension of the perfume capsules in the liquid components of the composition.

In a further aspect, the present invention is directed to a process for the preparation of a composition as herein described, characterized in that the at least one perfume oil, the at least one encapsulated perfume oil and the at least one stabilizer are mixed together.

In a further aspect, the present invention is directed to the use of at least one stabilizer selected from the group of the alk (en) ylsulfosuccinamates according to the present invention for stabilizing a composition comprising at least one free perfume oil and at least one encapsulated perfume oil.

In yet another aspect, the present invention is directed to a cosmetic product, a laundry or cleaning composition comprising at least one 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, unless otherwise stated,% by weight, in each case based on the total weight of the corresponding composition. Numeric ranges indicated 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 are also captured.

"At least one" as used herein refers to 1 or more, for example, 1, 2, 3, 4, 5, 6, 7, 8, 9 or more.

"Approximately" as used herein in numerical terms means the corresponding value ± 10%, preferably ± 5%, more preferably ± 3%, most preferably ± 1%.

A first object of the present invention is a composition which is preferably in the form of a suspension. The suspension comprises at least one free perfume oil, at least one encapsulated perfume oil and at least one stabilizer according to the present invention.

In the context of the present invention, the term "perfume oil" refers to individual perfume or perfume compounds or mixtures of several such compounds, and thus covers e.g. synthetic products of the ester type, ethers, aldehydes, ketones, alcohols and hydrocarbons, as well as natural fragrance mixtures as obtainable from vegetable sources.

In the context of the present invention, the term "free perfume oil" refers to a perfume oil which as such is present in a suspension as described herein, i. the individual constituents of the perfume oil are in particular not encapsulated.

A fragrance is an odor-causing chemical substance. In order to be able to stimulate the sense of smell, the chemical substance should be at least partially redistributable in the air, ie the fragrance should be at least slightly volatile at eg 25 ° C. If the fragrance is very volatile, the odor intensity sounds quickly again. With a lower volatility the odor impression is more sustainable, ie it does not disappear so fast. In one embodiment, therefore, the perfume has a melting point in the range of -100 ° C to 100 ° C, preferably from -80 ° C to 80 ° C, more preferably from -20 ° C to 50 ° C, especially of 30 ° C to 20 ° C. In a further embodiment, the perfume 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 is located.

Overall, a chemical substance should not exceed a certain molecular weight to act as a fragrance, since too high molecular mass, the required volatility can no longer be guaranteed. 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.

According to the present invention, a perfume may be an aldehyde, preferably selected from adoxal (2,6,10-trimethyl-9-undecenal), anisaldehyde (4-methoxybenzaldehyde), cymal (3- (4-isopropyl-phenyl 2-methylpropanal), ethylvanillin, florhydral (3- (3-isopropylphenyl) butanal), helional (3- (3,4-methylenedioxyphenyl) -2-methylpropanal), heliotropin, hydroxycitronellal, lauraldehyde, lyral (3- and 4-methylpropanal) - (4-hydroxy-4-methylpentyl) -3-cyclohexene-1-carboxaldehyde), methylnonylacetaldehyde, Lilial (3- (4-tert-butylphenyl) -2-methylpropanal), phenylacetaldehyde, undecylenealdehyde, vanillin, 2,6,10 Trimethyl-9-undecenal, 3-dodecen-1-al, alpha-n-amylcinnamaldehyde, 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-octadien-1-al, 3,7-dimethyl 1-6-octen-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-methylenedioxybenzaldehyde, alpha-n-hexylcinnamaldehyde, m-cymene-7-carboxaldehyde, alpha-methylphenylacetaldehyde, 7-hydroxy-3,7-dimethyloctanal, undecenal, 2 , 4,6-trimethyl-3-cyclohexene-1-carboxaldehyde, 4- (3) (4-methyl-3-pentenyl) -3-cyclohexenecarboxaldehyde, 1-dodecanal, 2,4-dimethylcyclohexene-3-carboxaldehyde, 4- (4-hydroxy-4-methylpentyl) -3-cyclohexene-1-carboxaldehyde, 7-methoxy-3,7-dimethyloctan-1-al, 2-methyl undecanal, 2-methyldecanal, 1-nonanal, 1-octanal, 2,6,10-trimethyl-5,9-undecadienal, 2-methyl-3- (4-tert-butyl) p ropanal, dihydrocinnamaldehyde, 1-methyl-4- (4-methyl-3-pentenyl) -3-cyclohexene-1-carboxaldehyde, 5- or 6-methoxy-hexahydro-4,7-methanindan-1 or 2-carboxaldehyde, 3 , 7-Dimethyloctan-1-al, 1-undecanal, 10-undecene-1-al, 4-hydroxy-3-methoxybenzaldehyde, 1-methyl-3- (4-methylpentyl) -3-cyclohexenecarboxaldehyde, 7-hydroxy-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-methanindane-1-carboxaldehyde, 2 Methyloctanal, alpha-methyl-4- (1-methylethyl) benzeneacetaldehyde, 6,6-dimethyl-2-norpinen-2-propionaldehyde, para-methylphenoxyacetaldehyde, 2-methyl-3-phenyl-2-propene-1-al, 3,5,5-trimethylhexanal, hexahydro-8,8-dimethyl-2-naphthaldehyde, 3-propyl-bicyclo [2.2.1] -hept-5-en-2-carbaldehyde, 9-decenal, 3-methyl- 5-phenyl-1-pentanal, methylnonylacetaldehyde, hexanal and / or trans-2-hexenal. It is also possible to use mixtures of the substances mentioned.

In a further embodiment, a perfume may be a ketone, preferably selected from methyl-beta-naphthyl ketone, muskedanone-1,2,3,5,6,7-hexahydro-1,1,2,3,3- pentamethyl-4H-inden-4-one), tartalide (6-acetyl-1,1,2,4,4,7-hexamethyltetralin), alpha-damascone, beta-damascone, delta-damascone, iso-damascone, damascenone, Methyl dihydrojasmonate, menthone, carvone, camphor, koavon (3,4,5,6,6-pentamethylhept-3-en-2-one), fenchone, alpha-ionone, betalonone, gamma-methyl-ionone, fleuramon (2-heptylcyclopene -tanone), dihydrojasmon, cis-jasmone, iso-E-Super (1- (1,2,3,4,5,6J, 8-octahydro-2,3,8,8-tetramethyl-2-naphthalenyl) - ethan-1-one (and isomers)), methyl cienyl ketone, acetophenone, methyl acetophenone, para-methoxy acetophenone, methyl beta-naphthyl ketone, benzyl acetone, benzophenone, para-hydroxyphenyl butanone, celery ketone (3-methyl-5-propyl-2-cyclohexenone ), 6-isopropyldecahydro-2-naphthone, dimethyloctenone, frescomethylene (2-butan-2-yl-cyclohexan-1-one), 4- (1-ethoxyvinyl) -3,3,5,5-tetramethylcyc 1-hexanone, methylheptenone, 2- (2- (4-methyl-3-cyclohexen-1-yl) -propyl) cyclopentanone, 1- (p-menthene-6 (2) yl) -1-propanone, 4- (4-hydroxy 3-methoxyphenyl) -2-butanone, 2-acetyl-3,3-dimethylnorbornane, 6,7-dihydro-1,1,2,3,3-pentamethyl-4 (5H) -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-heptadiene-3 -one), isocyclone E (2-acetonaphthone-1,2,3,4,5,6,7,8-octahydro-2,3,8,8-tetramethyl), methylnonyl ketone, methylcyclocitron, methyllavedelketone, Orivon (4-tert -Amylcyclohexanone), 4-tert-butylcyclohexanone, dolphone (2-pentylcyclopentanone), muscone (CAS 541-91-3), neobutenone (1- (5,5-dimethyl-1-cyclohexenyl) pent-4- en-1-one), Plicaton (CAS 41724-19-0), Veloutone (2,2,5-trimethyl-5-pentylcyclopentan-1-one), 2,4,4,7-tetramethyl-oct-6- en-3-one and / or tetrameran (6,10-dimethylundecen-2-one). It is also possible to use mixtures of the substances mentioned.

In a further embodiment, a perfume may be an alcohol, preferably selected from 10-undecen-1-ol, 2,6-dimethylheptan-2-ol, 2-methylbutanol, 2-methylpentanol, 2-phenoxyethanol, 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-decen-1-ol, α-methylbenzyl alcohol, α-terpineol, amyl salicylate, benzyl alcohol, Benzyl salicylate, β-terpineol, butyl salicylate, citronellol, cyclohexyl salicylate, decanol, di-hydromyrcenol, dimethylbenzylcarbinol, dimethylheptanol, dimethyloctanol, ethyl salicylate, ethylvaniline, eugenol, farnesol, geraniol, heptanol, 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 / or cinnamyl alcohol It is also possible to use mixtures of the substances mentioned.

In another embodiment, the fragrance may be a fragrance of natural or synthetic origin, e.g. of the type of esters, ethers, aldehydes, ketones, alcohols and hydrocarbons. Fragrance type ester compounds are e.g. Benzylacetate, phenoxyethylisobutyrate, p-tert-butylcyclohexylacetate, linalylacetate, dimethylbenzylcarbinylacetate (DMBCA), phenylethylacetate, benzylacetate, ethylmethylphenylglycinate, allylcyclohexylpropionate, styrallylpropionate, benzylsalicylate, cyclohexylsalicylate, floramate, melusate and jasmacyclate. The ethers include, for example, benzyl ethyl ether and ambroxane, to the aldehydes e.g. the linear alkanals of 8 to 18 carbon atoms, citral, citronellal, citronellyloxyacetaldehyde, cyclamen aldehyde (3- (4-propan-2-ylphenyl) butanal), lilial and bourgeonal, to the ketones e.g. the ionones, α-isomethylionone and methylcedryl ketone, the alcohols anethole, citronellol, eugenol, geraniol, linalool, phenylethyl alcohol and terpineol, the hydrocarbons mainly include terpenes such as limonene and pinene. Preferably, however, mixtures of different fragrances are used, which together produce an attractive fragrance.

In another embodiment, a fragrance may be an essential oil such as angelica root oil, aniseed oil, arnica blossom oil, basil oil, bayoil, champacilla oil, citrus oil, pinecone oil, pinecone oil, elemi oil, eucalyptus oil, fennel oil, pine needle oil, galbanum oil, geranium oil, ginger grass oil, guaiac wood oil , Gurjar balm oil, Helichrysum oil, Ho oil, ginger oil, iris oil, jasmin oil, cajeput oil, calamus oil, chamomile oil, camphor oil, kanaga oil, cardamom oil, cassia oil, pine oil, copaiba balsam, coriander oil, spearmint oil, caraway oil, cumin oil, labdanum oil, lavender oil, lemongrass oil, linden flower oil, lime oil , Tangerine oil, lemon 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, balsam oil, petitgrain oil, pepper oil, peppermint oil, pimento oil, pine oil, rose oil, rosemary oil, sage oil , Sandalwood l, celery oil, spiked oil, star aniseed oil, turpentine oil, thuja oil, thyme oil, verbena oil, vetiver oil, juniper berry oil, wormwood oil, wintergreen oil, ylang-ylang oil, hyssop oil, cinnamon oil, cinnamon oil, citronella oil, lemon oil and cypress oil, as well as ambrettolide, ambroxan, alpha Amyl cinnamaldehyde, 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, hydroxycinnamyl, indole, iron, isoeugenol, isoeugenol methyl ether, isosafrole, jasmon, camphor, Karvakrol, Karvon, p -Kresolmethylether, Coumarin, p-methoxyacetophenone, methyl-n-amyl ketone, methyl anthranilate, p-methylacetophenone, methylchavikole, p-methylquinoline, methyl-beta-naphthylketone, methyl-n-nonylacetaldehyde, methyl-n-nonylketone, muscone, beta-naphtholethylether, beta- Naphthol methyl ether, nerol, n-nonylaldehyde, nonyl alcohol, n-octylaldehyde, p-oxyacetophenone, pentadecanolide, beta-phenylethyl alcohol, phenylacetic acid, pulegone, safrole, isoamyl salicylate, salicylic acid methyl ester, salicylic acid hexyl ester, cyclohexyl salicylate, santalol, sandelice, skatole, terpineol, Thymen, thymol, troenan, gamma-undelactone, vanillin, veratrum aldehyde, cinnamaldehyde, cinnamyl alcohol, cinnamic acid, cinnamic acid ethyl ester, cinnamic acid benzyl ester, diphenyloxide, limonene, linalool, linalyl acetate and propionate, melusate, menthol, menthone, methyl-n-heptenone, pinene, phenylacetaldehyde , Terpinyl acetate, citral, citronellal and mixtures thereof. It is also possible to use mixtures of the substances mentioned.

It will be understood that all of the aforementioned fragrances and perfume mixtures may be combined with other perfumes and / or perfume mixtures to obtain the desired perfuming.

In various embodiments, the composition described herein contains the at least one free perfume oil in an amount of 10 to 98% by weight, preferably 50 to 95% by weight, based on the total weight of the composition.

Furthermore, the composition / suspension according to the present invention comprises at least one perfume oil which is in the form of an encapsulated perfume oil, i. in the form of perfume oil capsules.

In the context of the present invention, the term "encapsulated perfume oil" means a perfume oil which is present inside a capsule, i. it is not a free perfume oil. In this case, the at least one appropriately encapsulated perfume oil may be a perfume oil as defined above and may comprise one or more of the aforementioned perfumes.

A "capsule" within the meaning of the present invention is constructed, in particular, of a shell and a core, wherein in particular at least one perfume oil, as defined above, is present in the core, and optionally further advantageous agents, for example textile care agents. Here, the core may have a solid form, be liquid or viscous, ie, for example, be present as a melt or have a waxy structure. Both capsules in which the at least one perfume oil and, optionally, the other beneficial agent (s) is substantially contained in the pure substance are possible, as well as capsules in which the core is replaced by an at least one perfume oil and, optionally in which the further benefit agent (s) mixed or impregnated carrier is formed. Preferably, the core of the capsules is at temperatures below 120 °, preferably below 80 ° C, especially below 40 ° C liquid, viscous or at least meltable.

In the context of the present invention, particular preference is given to capsules having a mean diameter d ₅₀ of <250 μm, preferably 1 to 100 μm, preferably 5 to 80 μm, particularly preferably 10 to 50 μm and in particular 15 to 40 μm exhibit. The d ₅₀ value indicates the diameter which results when 50% by weight of the capsules have a smaller diameter and 50% by weight of the capsules have a larger diameter than the determined d ₅₀ value. It is furthermore preferred for the d ₉₀ value of the particle size distribution of the microcapsules to be <70 μm, preferably <60 μm, particularly preferably <50 m. The d ₉₀ value of the particle size distribution is the value at which 90% of all particles are smaller and 10% of the particles are larger than this value.

The determination of the diameter of the capsules or the particle size of the microcapsules can be carried out by conventional methods. It can be determined, for example, by means of dynamic light scattering, which is usually carried out on dilute suspensions, e.g. 0.01 to 1 wt .-% capsules, can be performed. It can also be done by evaluating light microscopic or electron micrographs of capsules.

As materials for the capsule wall are usually high molecular weight compounds, in particular polymers, in question, such. Proteins (e.g., gelatin, albumin, casein, and others), cellulose derivatives (e.g., methyl cellulose, ethyl cellulose, cellulose acetate, cellulose nitrate, carboxymethyl cellulose, and others), and especially synthetic polymers (e.g., polyamides, polyethylene glycols, polyurethanes, epoxy resins, and others). For example, melamine-urea-formaldehyde resins or melamine-formaldehyde resins or urea-formaldehyde resins may preferably be used as capsule wall materials.

The capsules can release the encapsulated fragrances via various mechanisms. They are e.g. Capsules can be used, which have a mechanically stable capsule shell, but then due to one or more environmental factors, such as change in temperature or ionic strength or the pH of the surrounding medium, for the contained funds is permeable. Also possible are stable capsule wall materials through which the at least one perfume oil as well as the one or more other benefit agents can diffuse through time. The capsules may release the at least one perfume oil and the further advantageous agent (s), preferably when the pH or ionic strength of the environment changes, as the temperature changes, upon exposure to light, through diffusion and / or under mechanical stress.

In a preferred embodiment of the present invention, the capsules are fragile, that is, they can contain entrapped agent due to mechanical stress such as friction, pressure or shearing stress breaking the shell of the capsules. In another preferred embodiment, the capsule is thermally labile, that is, entrapped materials may be released when the capsules are at a temperature of at least 70 ° C, preferably at least 60 ° C, more preferably at least 50 ° C, and most preferably at least 40 ° C is exposed.

In a further preferred embodiment, the capsule for the entrapped agent (at least one perfume oil and optionally one or more other benefit agents) may become permeable after exposure to radiation of a certain wavelength, preferably by the action of sunlight.

It is also possible that the capsules are fragile and at the same time thermally labile and / or unstable to radiation of a specific wavelength.

The capsules which can be used according to the invention may be water-soluble and / or water-insoluble capsules, but are preferably water-insoluble capsules. The water-insolubility of the capsules has the advantage that they can survive washing, cleaning or other treatment applications and thus be able to dispense the at least one perfume oil and other benefit agents only after the aqueous washing, cleaning or treatment process, such as for example, when drying by mere increase in temperature or by sunlight or in particular friction of the surface.

Particularly preferred are water-insoluble capsules which are broken up by friction, the wall material preferably comprising melamine-formaldehyde resins, polyurethanes, polyolefins, polyamides, polyureas, polyesters, polysaccharides, epoxy resins, silicone resins and / or polycondensation products of carbonyl compounds and compounds containing NH groups ,

The term "drippable" or "breakable by friction" capsules, means in particular those capsules, which, if they adhere to a surface treated therewith (eg textile surface) can be opened or broken by mechanical rubbing or by pressure, so that a Content release only results as a result of mechanical action, for example when one dries hands with a towel on which such capsules are deposited. Preferably usable, aufreibbare capsules have average diameter d ₅₀ in the range of 1 to 100 .mu.m, preferably between 5 and 95 .mu.m, in particular between 10 and 90 .mu.m, for example between 10 and 80 .mu.m, for example between 15 and 40 microns. The shell of the capsules enclosing the core or (filled) cavity preferably has an average thickness in the range between approximately 0.01 and 50 μm, preferably between approximately 0.1 μm and approximately 30 μm, in particular between about 0.5 μm and about 8 μm or about 5 μm. Capsules are particularly easy to squeeze if they are within the ranges given above regarding the average diameter and the average thickness.

Microcapsules with capsule walls of melamine-formaldehyde resins are particularly advantageous because of their excellent impermeability and mechanical stability.

Methods for microcapsule formation are known and, for example, in US 20030004226 A1 (BASF), which are hereby incorporated by reference.

Usually, during production, the core material, i. the at least one perfume oil, and optionally further benefit agents, in an aqueous solution of a protective colloid, which preferably has an acidic pH, emulsified into fine droplets. To the resulting emulsion is then added while mixing e.g. the aqueous solution of a melamine-formaldehyde precondensate or melamine and formaldehyde added individually for in-situ polymerization. This forms microcapsules. Upon completion of the addition, the condensation is completed. The capsules can be preformed, which is preferred, but also preformed, and then preferably by increasing the temperature (for example, temperature of at least about 40 ° C, preferably about 75 to 95 ° C) cure the capsule wall.

According to a preferred embodiment of the invention, the capsule dispersion according to the invention comprises water-insoluble microcapsules, preferably core-shell microcapsules, wherein the capsule walls in particular comprise melamine-formaldehyde resins. These microcapsules may contain, in addition to the at least one perfume oil, other liquids, but also readily solids, e.g. in the form of dispersions, for example, very fine hydrophobic silica dispersed in the at least one perfume oil.

• Texilpflegemittel wie Weichmacher, Phobier- und Imprägniermittel gegen Wasser und Wiederanschmutzungen, Bleichmittel, Bleichaktivatoren, Enzyme, Silikonöle, Antiredepositionsmittel, optische Aufheller, Vergrauungsinhibitoren, Einlaufverhinderer, Knitterschutzmittel, Farbübertragungsinhibitoren, antimikrobiellen Wirkstoffe, Germizide, Fungizide, Antioxidantien, Antistatika, Bügelhilfsmittel, Quell- und Schiebefestmittel, UV- Absorber, kationische Polymere,
• Behandlungsmittel für harte Oberflächen wie Desinfektionsmittel, Imprägnierungen gegen Wasser und Wiederanschmutzungen, Glanzförderer oder -Verhinderer, Hydrophobier- oder Hydrophiliermittel, Filmbildner,
• Hautpflegemittel (wie z.B. Vitamin E, natürliche Öle, Aloe- Vera-Extrakt, Grüner-Tee- Extrakt, D-Panthenol, Plankton Extrakt, Vitamin C, Harnstoff und/oder Glycin)
• Geruchsneutralisierer (z.B. umfassend Cyclodextrine, Cyclodextrin-Derivate, Triethylenglykol und/oder Natriumhydrogencarbonat)
• bakterienhemmende Wirkstoffe

verstanden.In various embodiments of the invention, the capsules may comprise, in addition to the at least one perfume oil, at least one benefit agent, such as in particular skin care agents, fabric care agents and / or odor neutralizers. In particular, the term benefit agent will be used

• Texilpflegemittel such as plasticizers, water repellents and impregnating agents, bleach, bleach activators, enzymes, silicone oils, anti redeposition agents, optical brighteners, grayness inhibitors, anti-shrink agents, anti-wrinkling agents, color transfer inhibitors, antimicrobial agents, germicides, fungicides, antioxidants, antistatic agents, ironing aids, swelling and Slip Resists, UV Absorbers, Cationic Polymers,
• Hard surface treating agents such as disinfectants, water and repellant impregnation, gloss enhancers or preventatives, water repellents or hydrophilicizers, film formers,
• Skin care products (such as vitamin E, natural oils, aloe vera extract, green tea extract, D-panthenol, plankton extract, vitamin C, urea and / or glycine)
• Odor neutralizer (eg comprising cyclodextrins, cyclodextrin derivatives, triethylene glycol and / or sodium bicarbonate)
• Bacteria-inhibiting agents

Understood.

1. a) Wachse wie Carnauba, Spermaceti, Bienenwachs, Lanolin, Derivate davon sowie Mischungen daraus;
2. b) Pflanzenextrakte, zum Beispiel pflanzliche Öle wie Avokadoöl, Olivenöl, Palmöl, Palmkernöl, Rapsöl, Leinöl, Sojaöl, Erdnussöl, Korianderöl, Ricinusöl, Mohnöl, Kakaoöl, Kokosnussöl, Kürbiskernöl, Weizenkeimöl, Sesamöl, Sonnenblumenöl, Mandelöl, Ma- cadamianussöl, Aprikosenkernöl, Haselnussöl, Jojobaöl oder Canolaöl, Kamille, Aloe Vera oder auch Grüner-Tee- oder Plankton-Extrakt sowie Mischungen daraus;
3. c) höhere Fettsäuren wie Laurinsäure, Myristinsäure, Palmitinsäure, Stearinsäure, Behensäure, Ölsäure, Linolsäure, Linolensäure, Isostearinsäure oder mehrfach ungesättigte Fettsäuren;
4. d) höhere Fettalkohole wie Laurylalkohol, Cetylalkohol, Stearylalkohol, Oleylalkohol, Behenylalkohol oder 2-Hexadecanol,
5. e) Ester wie Cetyloctanoat, Lauryllactat, Myristyllactat, Cetyllactat, Isopropylmyristat, Myristylmyristat, Isopropylpalmitat, Isopropyladipat, Butylstearat, Decyloleat, Cholesterolisostearat, Glycerolmonostearat, Glyceroldistearat, Glyceroltristearat, Alkyllactat, Alkylcitrat oder Alkyltartrat;
6. f) Kohlenwasserstoffe wie Paraffine, Mineralöle, Squalan oder Squalen;
7. g) Lipide;
8. h) Vitamine wie Vitamin A, C oder E oder Vitaminalkylester;
9. i) Phospholipide;
10. j) Sonnenschutzmittel wie Octylmethoxylcinnamat und Butylmethoxybenzoylmethan;
11. k) Silikonöle wie lineare oder cyclische Polydimethylsiloxane, Amino-, Alkyl-, Alkylaryl- oder Aryl-substituierte Silikonöle und
12. l) Mischungen daraus

umfassen.The skin care composition (skin care agent) is preferably hydrophobic, may be liquid or solid. For example, the skin care compound

1. a) waxes such as carnauba, spermaceti, beeswax, lanolin, derivatives thereof and mixtures thereof;
2. 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, casadamian nut oil, apricot kernel oil , Hazelnut oil, jojoba oil or canola oil, chamomile, aloe vera or even green tea or plankton extract, and mixtures thereof;
3. 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;
4. d) higher fatty alcohols, such as lauryl alcohol, cetyl alcohol, stearyl alcohol, oleyl alcohol, behenyl alcohol or 2-hexadecanol,
5. 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;
6. f) hydrocarbons such as paraffins, mineral oils, squalane or squalene;
7. g) lipids;
8. h) vitamins such as vitamins A, C or E or vitamin alkyl esters;
9. i) phospholipids;
10. j) sunscreens such as octyl methoxyl cinnamate and butyl methoxybenzoyl methane;
11. k) silicone oils such as linear or cyclic polydimethylsiloxanes, amino-, alkyl-, alkylaryl- or aryl-substituted silicone oils and
12. l) mixtures thereof

include.

According to the present invention, the at least one encapsulated perfume oil is usually in the form of a (capsule) slurry, i. a slurry of the capsules in a liquid medium.

The term "slurry" in the context of the present invention refers to a, typically aqueous, slurry of perfume capsules as defined above. The liquid medium preferably consists predominantly, ie more than 50 wt .-% of water, but can also completely, ie 100% water. The slurry is preferably pourable, ie it can be poured out of a vessel by tilting the vessel. A castable slurry is understood as meaning, in particular, a capsule / liquid mixture which has a viscosity of less than 10-10 ⁴ mPas (Brookfield rotational viscometer, spindle 2, 20 U, in particular at a maximum of 40 ° C., in particular not more than 20 ° C. / min.).

The slurry may contain other auxiliaries, for example those which ensure a certain durability or stability. Frequently used adjuvants include, for example, surfactants, especially anionic and / or nonionic surfactants. Corresponding capsule slurries are commercially available and known to those skilled in the art.

In various embodiments, the capsules described above in an amount of 1 to 50 wt .-%, preferably 20 to 48 wt .-%, in particular 35 to 45 wt .-% in the slurry.

In various embodiments, the composition according to the invention is characterized in that the at least one encapsulated perfume oil in the form of a capsule slurries in an amount of 2 to 90 wt .-%, preferably from 3 to 70 wt .-%, more preferably 4 to 50 wt. % based on the total weight of the composition is contained in this. Accordingly, in consideration of the fact that the slurry preferably contains the capsules only in an amount of from 1 to 50, in particular from 20 to 48,% by weight, the proportion of capsules in various embodiments is from 0.02 to 45, preferably from 0.4 to 43.2, more preferably 0.6 to 33.6 wt .-% based on the total weight of the composition.

In various embodiments, the weight ratio of the at least one free perfume oil to the capsule slurry as described above is from 10:90 to 98: 2, preferably from 50:50 to 95: 5.

The perfume oil capsule suspension according to the present invention further comprises at least one stabilizer selected from the group consisting of alk (en) ylsulfosuccinamates according to the present invention.

The stabilizer serves to stably disperse the capsules in the composition.

In various embodiments, the at least one stabilizer is contained in an amount of from 0.05 to 10% by weight, preferably in an amount of from 0.5 to 5% by weight, based on the total weight in the composition.

As already mentioned above, the composition according to the invention is preferably in the form of a suspension of the capsules in a continuous, liquid phase. The suspension is preferably stable, i. It also comes after prolonged storage periods of for example several days to weeks at usual temperatures in the range up to 40 ° C, for example 4 weeks at a temperature between> 0 and 40 ° C, not agglomeration, sedimentation and / or floating of the capsules or a other phase separation. In various embodiments, the composition contains water, which is introduced, for example, via the capsule slurry. The water content may be, in various embodiments, from about 5 to 50 wt .-%, preferably 5 to 40 wt .-% amount. In such embodiments, water may form the continuous phase in which the capsules and optionally also the perfume oil are (stably) dispersed, i. the suspension is an aqueous suspension. It should be noted here that even in embodiments in which the water phase does not constitute the main portion of the liquid phase, for example, the perfume oil may be contained in a relatively larger amount, the water phase may form the continuous phase in which the other phase suspends or emulsifies are.

In various embodiments, the composition as described above is further characterized by having a viscosity of from 50 to 5000 mPas, preferably from 100 to 3000 mPas (Brookfield rotational viscometer, spindle 2, 20 rpm).

In addition, the composition / suspension may additionally contain further ingredients which are typically contained in detergents or cleansing products or cosmetic products. For example, in one embodiment, the perfume oil capsule suspension contains, in addition to the at least one free perfume oil, at least one encapsulated perfume oil in the form of a capsule slurries and the at least one stabilizer as described herein, one or more dyes (e ). The dyes may be present in an amount of 0.01-5 wt .-% in the composition.

The present invention further provides a process for preparing a composition, ie a perfume oil capsule suspension as described above, characterized in that the at least one perfume oil containing at least one encapsulated perfume oil in the form of a capsule slurries and the at least one Stabilizer are mixed together. Suitable methods of mixing the foregoing components are known in the art and may include, for example, mixing in a homogenizer. In the event that one or more of the aforementioned components are not liquid at room temperature, the respective components may be heated prior to mixing with the remaining components, for example at temperatures between 20 ° C to 100 ° C, preferably between 25 ° C and 60 ° C to facilitate mixing with the other components.

The present invention further relates to the use of the above-described stabilizers for stabilizing a perfume oil capsule suspension as described herein.

The perfume oil capsule suspension as described herein may be part of a cosmetic product. The present invention therefore also provides a cosmetic product containing at least one perfume oil capsule suspension as described herein. Particularly advantageous are the stabilized according to the present invention perfume capsule suspensions in the manufacture of detergents or cleaning agents. The present invention therefore further provides a washing or cleaning agent containing at least one perfume capsule suspension as described herein.

Suitable in this context are all conceivable types of detergents or cleaners, both concentrates and undiluted agents, for use on a commercial scale, in the washing machine or in hand washing or cleaning. These include detergents for textiles, carpets, or natural fibers, for which the term detergent is used. These include, for example, dishwashing detergents for dishwashers or manual dishwashing detergents or cleaners for hard surfaces such as metal, glass, porcelain, ceramics, tiles, stone, painted surfaces, plastics, wood or leather, for which the term detergent is used, ie in addition to manual and machine Dishwashing agents, for example, scouring agents, glass cleaners, toilet scenters, etc. The washing and cleaning agents in the invention also include washing aids which are added to the actual detergent in the manual or machine textile laundry to achieve a further effect. Furthermore, laundry detergents and cleaners in the context of the invention also include textile pre-treatment and post-treatment agents, ie those agents with which the laundry item is brought into contact before the actual laundry, for example to dissolve stubborn soiling, and also agents which are in one of the actual Textile laundry downstream step to give the laundry further desirable properties such as comfortable grip, crease resistance or low static charge. Among the latter, i.a. calculated the fabric softener.

The present invention likewise relates to a process in which a liquid detergent or cleaning agent is mixed with a perfume capsule suspension as described above, preferably by stirring the perfume capsule suspensions into the washing or cleaning agent matrix or by continuous Add in a liquid washing or cleaning agent and mixing via static mixing elements.

A further subject of the present invention is also a process in which a solid washing or cleaning agent with a perfume capsule suspensions, as described herein, is mixed, for example by spraying the perfume capsule suspensions to the solid detergent or cleaning agent.

The amount in which the perfume oil capsule suspension as described herein can be present in a washing or cleaning agent is between 0.5 to 40% by weight, preferably between 1 to 30% by weight, especially between 5 to 15 wt .-%, based on the total weight of the washing or cleaning agent.

In addition to the perfume capsule suspensions as described herein, the washing or cleaning agent further contains conventional and known in the art as other ingredients, for example at least one or preferably more substances from the group of enzymes, surfactants, bleaching agents, complexing agents, builders, electrolytes , nonaqueous solvents, pH adjusters, other fragrances, other fragrance carriers, fluorescers, dyes, hydrotropes, foam inhibitors, silicone oils, anti redeposition agents, grayness inhibitors, shrinkage inhibitors, anti-crease agents, dye transfer inhibitors, antimicrobial agents, germicides, fungicides, antioxidants, corrosion inhibitors, antistatic agents, bittering agents, ironing aids , Repellents and impregnating agents, swelling and anti-slip agents, softening components and UV absorbers.

All aspects, objects, and embodiments described for compositions / suspensions described herein are also applicable to the aforementioned methods, uses, and compositions containing these compositions. Therefore, reference is made at this point expressly to the disclosure in the appropriate place with the statement that this disclosure also applies to the above described methods and uses.

Examples

• 63,7 % Parfümöl 07-10353
• 2,0 % Di-Na-Sulfosuccinamat (C18)
• 34,3 % FS Slurry 12-11723 Fresh Boost V2 (Parfümkapsel-Slurry)

Example 1: Mixing ratio 65% perfume, 35% capsule slurry containing 41% capsules Formulation:

• 63.7% perfume oil 07-10353
• 2.0% di-Na sulfosuccinamate (C18)
• 34.3% FS Slurry 12-11723 Fresh Boost V2 (Perfume Capsule Slurry)

1. 1) Di-Na-Sulfosuccinamat (C18) wird auf 70 °C erwärmt
2. 2) Dosierung von Di-Na-Sulfosuccinamat (C18) in das Parfümöl
3. 3) Ultra Turrax einschalten
4. 4) Dosierung verkapseltes Parfümöl zu obenstehender Mischung
5. 5) 1 Minute Nachrührzeit

Phasenstabilität Lagerintervall Startwert 4 Wochen 5 °C 4 Wochen 20 °C 4 Wochen 40 °C Parfümöl 07-10353 stabil stabil stabil stabil Verkapseltes Parfümöl FS Slurry 12-11723 Fresh Boost V2 stabil Phasentrennung Phasentrennung Phasentrennung Parfümöl-Kapsel-Suspension stabil stabil stabil stabil Geruchsbewertung (Lagerung Parfümöl-Kapsel-Suspension) 0,65 % Parfümöl 07-10353 Rose Rain + 0,35 % FS Slurry 12-11723 1,00 % Parfümöl-Kapsel-Suspension 65:35 Startwert 1,00 % Parfümöl-Kapsel-Suspension 65:35 2 Wochen 5 °C 1,00 % Parfümöl-Kapsel-Suspension 65:35 2 Wochen RT 1,00 % Parfümöl-Kapsel-Suspension 65:35 2 Wochen 40 °C Produkt 7 7 7 7 7 Feuchte Wäsche 7 7 7 7 7 Trockene Wäsche 7 7 7 7 7 Boost Effekt 5 5 5 5 5 production:

1. 1) Di-Na sulfosuccinamate (C18) is heated to 70 ° C
2. 2) Dosing of di-Na-sulfosuccinamate (C18) in the perfume oil
3. 3) Turn on Ultra Turrax
4. 4) Dosage encapsulated perfume oil to top mix
5. 5) 1 minute stirring time

phase stability bearing interval start value 4 weeks 5 ° C 4 weeks 20 ° C 4 weeks 40 ° C Perfume oil 07-10353 stable stable stable stable Encapsulated perfume oil FS Slurry 12-11723 Fresh Boost V2 stable phase separation phase separation phase separation Perfume oil capsule suspension stable stable stable stable 0.65% perfume oil 07-10353 Rose Rain + 0.35% FS Slurry 12-11723 1.00% perfume oil capsule suspension 65:35 starting value 1.00% perfume oil capsule suspension 65:35 2 weeks 5 ° C 1.00% perfume oil capsule suspension 65:35 2 weeks RT 1.00% perfume oil capsule suspension 65:35 2 weeks 40 ° C product 7 7 7 7 7 Wet laundry 7 7 7 7 7 Dry laundry 7 7 7 7 7 Boost effect 5 5 5 5 5

• 19,6 % Parfümöl 99-6236
• 2,0 % Di-Na-Sulfosuccinamat (C18)
• 78,4 % FS Slurry 12-11723 Fresh Boost V2

Example 2: Mixing ratio 20% perfume, 80% capsule slurry containing 41% capsules Formulation:

• 19.6% perfume oil 99-6236
• 2.0% di-Na sulfosuccinamate (C18)
• 78.4% FS Slurry 12-11723 Fresh Boost V2

1. 1) Di-Na-Sulfosuccinamat (C18) wird auf 70 °C erwärmt
2. 2) Dosierung von Di-Na-Sulfosuccinamat (C18) in das Parfümöl
3. 3) Ultra Turrax einschalten
4. 4) Dosierung verkapseltes Parfümöl zu obenstehender Mischung
5. 5) 1 Minute Nachrührzeit

Phasenstabilität Lagerintervall Startwert 4 Wochen 5 °C 4 Wochen 20 °C 4 Wochen 40 °C Parfümöl 99-6236 stabil stabil stabil stabil Verkapseltes Parfümöl FS Slurry 12-11723 Fresh Boost V2 stabil Phasentrennung Phasentrennung Phasentrennung Parfümöl-Kapsel-Suspension stabil stabil stabil stabil Geruchsbewertung (Lagerung Parfümöl-Kapsel-Suspension) 0,20 % Parfümöl 99-6236 Flower Power + 0,80 % FS Slurry 1,00 % Parfümöl-Kapsel-Suspension 20:80 Startwert 1,00 % Parfümöl-Kapsel-Suspension 20:80 2 Wochen 5 °C 1,00 % Parfümöl-Kapsel-Suspension 20:80 2 Wochen RT 1,00 % Parfümöl-Kapsel-Suspension 20:80 2 Wochen 40 °C Produkt 8 8 8 8 8 Feuchte Wäsche 8 8 8 8 8 Trockene Wäsche 7 7 7 7 7 Boost Effekt 5 5 5 5 5 production:

1. 1) Di-Na sulfosuccinamate (C18) is heated to 70 ° C
2. 2) Dosing of di-Na-sulfosuccinamate (C18) in the perfume oil
3. 3) Turn on Ultra Turrax
4. 4) Dosage encapsulated perfume oil to top mix
5. 5) 1 minute stirring time

phase stability bearing interval start value 4 weeks 5 ° C 4 weeks 20 ° C 4 weeks 40 ° C Perfume oil 99-6236 stable stable stable stable Encapsulated perfume oil FS Slurry 12-11723 Fresh Boost V2 stable phase separation phase separation phase separation Perfume oil capsule suspension stable stable stable stable 0.20% Perfume Oil 99-6236 Flower Power + 0.80% FS Slurry 1.00% perfume oil capsule suspension 20:80 starting value 1.00% perfume oil capsule suspension 20:80 2 weeks 5 ° C 1.00% perfume oil capsule suspension 20:80 2 weeks RT 1.00% perfume oil capsule suspension 20:80 2 weeks 40 ° C product 8th 8th 8th 8th 8th Wet laundry 8th 8th 8th 8th 8th Dry laundry 7 7 7 7 7 Boost effect 5 5 5 5 5

• 89,5 % Parfümöl 9907-10353 Rose Rain
• 1,0 % Hydriertes Rizinusöl, ethoxyliert
• 9,5 % FS Slurry 12-11641 Fougere Caps 50 % DIF

Example 3: Mixing ratio 90% perfume, 10% capsule slurry containing 41% capsules Formulation:

• 89.5% perfume oil 9907-10353 Rose Rain
• 1.0% hydrogenated castor oil, ethoxylated
• 9.5% FS Slurry 12-11641 Fougere Caps 50% DIF

1. 1) Hydriertes Rizinusöl, ethoxyliert, bei 50 °C aufschmelzen
2. 2) Verkapseltes Parfümöl vorlegen
3. 3) Ultra Turrax einschalten
4. 4) Parfümöl hinzugeben
5. 5) 1 Minute homogenisieren
6. 6) Dosierung von hydriertem Rizinusöl
7. 7) 1 Minute Nachrührzeit

Phasenstabilität Lagerintervall Startwert 4 Wochen 5 °C 4 Wochen 20 °C 4 Wochen 40 °C Parfümöl 07-10353 stabil stabil stabil stabil Verkapseltes Parfümöl FS Slurry 12-11641 Fougere Caps 50 % DIF stabil Phasentrennung Phasentrennung Phasentrennung Parfümöl-Kapsel-Suspension stabil stabil stabil stabil production:

1. 1) Hydrogenated castor oil, ethoxylated, melt at 50 ° C
2. 2) Submit encapsulated perfume oil
3. 3) Turn on Ultra Turrax
4. 4) Add perfume oil
5. 5) Homogenize for 1 minute
6. 6) Dosage of hydrogenated castor oil
7. 7) 1 minute stirring time

phase stability bearing interval start value 4 weeks 5 ° C 4 weeks 20 ° C 4 weeks 40 ° C Perfume oil 07-10353 stable stable stable stable Encapsulated Perfume Oil FS Slurry 12-11641 Fougere Caps 50% DIF stable phase separation phase separation phase separation Perfume oil capsule suspension stable stable stable stable

Claims (11)

Composition, characterized in that the composition comprises at least one free perfume oil, at least one encapsulated perfume oil and at least one stabilizer selected from the group consisting of alk (en) ylsulfosuccinamaten according to formula I.

wherein R is C ₈ to C ₁₈ alkyl or C ₈ to C ₁₈ alkenyl, and where M ⁺ is Na ⁺ , K ⁺ or NH ₄ ⁺ ; includes. The composition according to claim 1, characterized in that the at least one free perfume oil is contained in an amount of 10 to 98% by weight, preferably 50 to 95% by weight, based on the total weight in the composition. The composition according to claim 1 or 2, characterized in that the at least one encapsulated perfume oil is in the form of a capsule slurry. The composition according to claim 3, characterized in that the capsule slurry in an amount of 2 to 90 wt .-%, preferably from 3 to 70 wt .-%, more preferably 5 to 50 wt .-% in relation to the Total weight is included in the composition. The composition according to claim 3 or 4, characterized in that the capsules in an amount of 1 to 50 wt .-%, preferably 20 to 48 wt .-%, in particular 35 to 45 wt .-% are contained in the slurry. The composition according to one of the preceding claims, characterized in that the composition is in the form of an aqueous suspension and the water content is preferably from 5 to 50% by weight, based on the total weight of the composition. The composition according to any one of the preceding claims, characterized in that the at least one stabilizer is selected from the group consisting of alk (en) ylsulfosuccinamaten according to formula (I), wherein R is C18 alkenyl. The composition according to one of the preceding claims, characterized in that the at least one suspension stabilizer is present in an amount of 0.05 to 10% by weight, preferably in an amount of 0.5 to 5% by weight in the composition on the total weight of the composition. Composition comprising at least one composition according to one of claims 1 to 8, wherein the agent is a cosmetic product, washing or cleaning agent. Use of a stabilizer selected from the group consisting of alk (en) ylsulfosuccinamaten according to formula I.

wherein R is C ₈ to C ₁₈ alkyl or C ₈ to C ₁₈ alkenyl, and where M ⁺ is Na ⁺ , K ⁺ or NH ₄ ⁺ ; for stabilizing a composition comprising at least one free perfume oil and at least one encapsulated perfume oil. A process for the preparation of a composition according to any one of claims 1 to 8, wherein the at least one free perfume oil is initially charged and to which the at least one encapsulated perfume oil and the at least one stabilizer are added.