Benefit agent delivery compositions

Benefit agent delivery compositions, compositions, packaged products and displays comprising such benefit agent delivery compositions, and processes for making and using such benefit agent delivery compositions, compositions, packaged products and displays. Such compositions have improved deposition and retention properties that may impart improved benefit characteristics to a composition and/or situs.

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Description
CROSS-REFERENCES TO RELATED APPLICATIONS

This application claims priority under 35 U.S.C. §119(e) to U.S. Provisional Application Ser. No. 60/901,569 filed Feb. 15, 2007.

FIELD OF INVENTION

The present application relates to benefit agent delivery compositions, compositions, packaged products and displays comprising such benefit agent delivery compositions, and processes for making and using such benefit agent delivery compositions and compositions, packaged products and displays comprising such benefit agent delivery compositions.

BACKGROUND OF THE INVENTION

Benefit agents, such as perfumes, brighteners, insect repellants, silicones, waxes, flavors, vitamins and fabric softening agents, skin care agents are expensive and may be less effective when employed at high levels in personal care compositions, cleaning compositions, and fabric care compositions. As a result, there is a desire to maximize the effectiveness of such benefit agents. One method of achieving such objective is to improve the delivery efficiencies of such benefit agents. Unfortunately, it is difficult to improve the delivery efficiencies of benefit agents as such agents may be lost do to the agents' physical or chemical characteristics, such agents may be incompatible with other compositional components or the situs that is treated, or such agents may be lost during post application processes such as rinsing or drying.

Accordingly, there is a need for a benefit agent delivery composition that provides improved benefit agent delivery efficiency. While not being bound by theory, applicants believe that the benefit agent delivery compositions disclosed herein meet such need as such compositions have increased deposition and retention properties which result in the desired increase in benefit agent delivery efficiency.

SUMMARY OF THE INVENTION

Benefit agent delivery compositions, compositions, packaged products and displays comprising such benefit agent delivery compositions, and processes for making and using such benefit agent delivery compositions, and compositions, packaged products and displays comprising such benefit agent delivery compositions.

DETAILED DESCRIPTION OF THE INVENTION Definitions

As used herein “consumer product” means baby care, beauty care, fabric & home care, family care, feminine care, health care, snack and/or beverage products or devices intended to be used or consumed in the form in which it is sold, and not intended for subsequent commercial manufacture or modification. Such products include but are not limited to diapers, bibs, wipes; products for and/or methods relating to treating hair (human, dog, and/or cat), including, bleaching, coloring, dyeing, conditioning, shampooing, styling; deodorants and antiperspirants; personal cleansing; cosmetics; skin care including application of creams, lotions, and other topically applied products for consumer use; and shaving products, products for and/or methods relating to treating fabrics, hard surfaces and any other surfaces in the area of fabric and home care, including: air care, car care, dishwashing, fabric conditioning (including softening), laundry detergency, laundry and rinse additive and/or care, hard surface cleaning and/or treatment, and other cleaning for consumer or institutional use; products and/or methods relating to bath tissue, facial tissue, paper handkerchiefs, and/or paper towels; tampons, feminine napkins; products and/or methods relating to oral care including toothpastes, tooth gels, tooth rinses, denture adhesives, tooth whitening; over-the-counter health care including cough and cold remedies, pain relievers, RX pharmaceuticals, pet health and nutrition, and water purification; processed food products intended primarily for consumption between customary meals or as a meal accompaniment (non-limiting examples include potato chips, tortilla chips, popcorn, pretzels, corn chips, cereal bars, vegetable chips or crisps, snack mixes, party mixes, multigrain chips, snack crackers, cheese snacks, pork rinds, corn snacks, pellet snacks, extruded snacks and bagel chips); and coffee.

As used herein, the term “cleaning and/or treatment composition” includes, unless otherwise indicated, granular or powder-form all-purpose or “heavy-duty” washing agents, especially cleaning detergents; liquid, gel or paste-form all-purpose washing agents, especially the so-called heavy-duty liquid types; liquid fine-fabric detergents; hand dishwashing agents or light duty dishwashing agents, especially those of the high-foaming type; machine dishwashing agents, including the various tablet, granular, liquid and rinse-aid types for household and institutional use; liquid cleaning and disinfecting agents, including antibacterial hand-wash types, cleaning bars, mouthwashes, denture cleaners, dentifrice, car or carpet shampoos, bathroom cleaners; hair shampoos and hair-rinses; shower gels and foam baths and metal cleaners; as well as cleaning auxiliaries such as bleach additives and “stain-stick” or pre-treat types, substrate-laden products such as dryer added sheets, dry and wetted wipes and pads, nonwoven substrates, and sponges; as well as sprays and mists.

As used herein, the term “fabric care composition” includes, unless otherwise indicated, fabric softening compositions, fabric enhancing compositions, fabric freshening compositions and combinations there of.

As used herein, the term “amine” includes, unless otherwise indicated, primary, secondary, tertiary, and quaternary amines.

As used herein, the articles such as “a” and “an” when used in a claim, are understood to mean one or more of what is claimed or described.

As used herein, the terms “include”, “includes” and “including” are meant to be synonymous with the phrase “including but not limited to”.

As used herein, the term “solid” includes granular, powder, bar and tablet product forms.

As used herein, the term “situs” includes paper products, fabrics, garments, hard surfaces, hair and skin.

Unless otherwise noted, all component or composition levels are in reference to the active portion of that component or composition, and are exclusive of impurities, for example, residual solvents or by-products, which may be present in commercially available sources of such components or compositions.

All percentages and ratios are calculated by weight unless otherwise indicated. All percentages and ratios are calculated based on the total composition unless otherwise indicated.

It should be understood that every maximum numerical limitation given throughout this specification includes every lower numerical limitation, as if such lower numerical limitations were expressly written herein. Every minimum numerical limitation given throughout this specification will include every higher numerical limitation, as if such higher numerical limitations were expressly written herein. Every numerical range given throughout this specification will include every narrower numerical range that falls within such broader numerical range, as if such narrower numerical ranges were all expressly written herein.

Benefit Agent Delivery Compositions

In one aspect, benefit agent delivery compositions comprising a benefit agent, a polymeric material and an optional cross-linker are disclosed.

Such benefit agent delivery compositions may comprise from about 54% to about 95%, from about 30% to about 85%, or even from about 40% to about 60% of a benefit agent; from about 5% to about 70%, from about 20 to about 60%, or even from about 30% to about 55% of a polymeric compound containing a carboxylic acid moiety; and from about 0% to about 50%, from about 0% to about 10%, or even from about 1% to about 7% by weight of a cross-linking agent.

Suitable benefit agents include silicones, enzymes, fragrances, perfumes, perfume raw materials, fragrance raw materials, deodorants, odor counteractants, malodors, essential oils, ethers, esters, ketones, alcohols, glycols, silicone hydrocarbons, cyclic hydrocarbons, aldehydes, terpines, volatile or nonvolatile insecticides, volatile or nonvolatile insect repellants, volatile or nonvolatile pesticides, volatile or nonvolatile antimicrobial agents, volatile or nonvolatile fungicides, volatile or nonvolatile herbicides and mixtures thereof. In one aspect, the inclusion of volatile or nonvolatile acids is avoided to reduce the potential of the cross reaction of the acid with the cross-linker.

In one aspect, the benefit agent comprises a perfume raw material, a fragrance, a perfume, an essential oil, an insecticide, an insect repellant, a pesticide, a herbicide, an odorant, a malodor counteractant, an odor masking agent, a cooling agent, a vitamin, softening agent, a skin care agent, a silicone, a softening agent, an encapsulated perfume and combinations thereof.

In one aspect, the benefit agent comprises a fragrance and/or a perfume. Useful perfume materials include materials selected from the group consisting of Table 1 Perfumes, Table 2 Perfumes, Table 3 Perfumes and mixtures thereof.

TABLE 1 Perfumes Number Registry Name Trade Name 1 Propanoic acid, ethyl ester Ethyl Propionate 2 Acetic acid, 2-methylpropyl ester Isobutyl Acetate 3 Butanoic acid, ethyl ester Ethyl Butyrate 4 Butanoic acid, 2-methyl-, ethyl ester Ethyl-2-Methyl Butyrate 5 2-Hexenal, (E)- 2-Hexenal 6 1-Butanol, 3-methyl-, acetate Iso Amyl-Acetate 7 2-Buten-1-ol, 3-methyl-, acetate Prenyl Acetate 8 2-Hexen-1-ol Beta Gamma Hexenol 9 3-Hexen-1-ol Beta Gamma Hexenol 10 Benzaldehyde Benzaldehyde 11 3-Hexen-1-ol, acetate, (Z)- Cis 3 Hexenyl Acetate 12 Benzoic acid, methyl ester Methyl Benzoate 13 Benzeneacetaldehyde Phenyl Acetaldehyde 14 Benzeneacetic acid, methyl ester Methyl Phenyl Acetate 15 1,3-Dioxolane-2-acetic acid, 2-methyl-, ethyl Fructone ester 16 Benzeneacetaldehyde, .alpha.-methyl- Hydratropic Aldehyde 17 3-Cyclohexene-1-carboxaldehyde, 3,5- Cyclal C, dimethyl- 18 Acetic acid, (2-methylbutoxy)-, 2-propenyl Allyl Amyl Glycolate ester 19 Benzenemethanol, .alpha.-methyl-, acetate Methyl Phenyl Carbinyl Acetate 20 Acetic acid, (3-methylbutoxy)-, 2-propenyl Allyl Amyl Glycolate ester 21 Benzaldehyde, 4-methoxy- Anisic Aldehyde 22 Benzeneacetic acid, ethyl ester Ethyl Phenyl Acetate 23 2-Cyclohexen-1-one, 2-methyl-5-(1- Laevo Carvone methylethenyl)-, (R)- 24 Ethanol, 2,2′-oxybis- Calone 161 25 Acetic acid, 2-phenylethyl ester Phenyl Ethyl Acetate 26 Benzoic acid, 2-amino-, methyl ester Methyl Anthranilate 27 4,7-Methano-1H-inden-6-ol, 3a,4,5,6,7,7a- Flor Acetate hexahydro-, acetate 28 Octanal, 7-hydroxy-3,7-dimethyl- Hydroxycitronellal 29 2(3H)-Furanone, 5-ethyldihydro- Gamma Hexalactone 30 Phenol, 4-methyl- Para Cresol 31 Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, Camphor Gum (1R)- 32 2H-Pyran, 3,6-dihydro-4-methyl-2-(2-methyl-1- Nerol Oxide propenyl)- 33 Benzeneethanol, .beta.-methyl- Hydratropic Alcohol 34 Benzeneethanol, .alpha.,.alpha.-dimethyl- Dimethyl Benzyl Carbinol 35 Benzoic acid, 2-(methylamino)-, methyl ester Dimethyl Anthranilate 36 2-Propenal, 3-phenyl- Cinnamic Aldehyde 37 2-Propenoic acid, 3-phenyl-, methyl ester Methyl Cinnamate 38 4H-Pyran-4-one, 2-ethyl-3-hydroxy- Ethyl Maltol 39 Acetic acid ethyl ester Ethyl Acetate 40 2-Heptanone Methyl Amyl Ketone 41 Acetic acid, pentyl ester Iso Amyl-Acetate 42 3-Octanone Ethyl Amyl Ketone 43 2-Octanone Methyl Hexyl Ketone 44 Heptenone, methyl- Methyl Heptenone 45 1-Heptanol Heptyl Alcohol 46 5-Hepten-2-one, 6-methyl- Methyl Heptenone 47 Butanoic acid, 3-oxo-, ethyl ester Ethyl Acetoacetate 48 Ethanol, 2-(2-methoxyethoxy)- Veramoss Sps 49 Tricyclo[2.2.1.02,6]heptane, 1-ethyl-3- Neoproxen methoxy- 50 Benzene, 1,4-dimethoxy- Hydroquinone Dimethyl Ether 51 Carbonic acid, 3-hexenyl methyl ester, (Z)- Liffarome 52 Oxirane, 2,2-dimethyl-3-(3-methyl-2,4- Myroxide pentadienyl)- 53 Ethanol, 2-(2-ethoxyethoxy)- Diethylene Glycol Mono Ethylether 54 Cyclohexaneethanol Cyclohexyl Ethyl Alcohol 55 3-Octen-1-ol, (Z)- Octenol Dix 56 3-Cyclohexene-1-carboxaldehyde, 3,6- Cyclovertal dimethyl- 57 1,3-Oxathiane, 2-methyl-4-propyl-, cis- Oxane 58 Acetic acid, 4-methylphenyl ester Para Cresyl Acetate 59 Benzene, (2,2-dimethoxyethyl)- Phenyl Acetaldehyde Dimethyl Acetal 60 Ethanone, 1-(4-methylphenyl)- Para Methyl Acetophenone 61 Propanoic acid, phenylmethyl ester Benzyl Propionate 62 Octanal, 7-methoxy-3,7-dimethyl- Methoxycitronellal Pq 63 Linalool oxide Linalool Oxide 64 2H-1-Benzopyran-2-one, octahydro- Octahydro Coumarin 65 Benzenepropanal, .beta.-methyl- Trifernal 66 4,7-Methano-1H-indenecarboxaldehyde, Formyltricyclodecan octahydro- 67 2-Butanone, 4-phenyl- Benzyl Acetone 68 Ethanone, 1-(4-methoxyphenyl)- Para Methoxy Acetophenone 69 Benzoic acid, 2-hydroxy-, methyl ester Methyl Salicylate USP 70 Propanenitrile, 3-(3-hexenyloxy)-, (Z)- Parmanyl 71 1,4-Methanonaphthalen-5(1H)-one, Tamisone 4,4a,6,7,8,8a-hexahydro- 72 Benzene, [2-(2-propenyloxy)ethyl]- LRA 220 73 Benzenepropanol Phenyl Propyl Alcohol 74 Ethanol, 2-phenoxy- Phenoxyethanol 75 1H-Indole Indole 76 1,3-Dioxolane, 2-(phenylmethyl)- Ethylene Glycol Acetal/Phenyl Acetaldehy 77 2H-1-Benzopyran-2-one, 3,4-dihydro- Dihydrocoumarin

In one aspect, suitable Table 1 perfume raw materials include perfume raw materials from number 1 to number 39 and mixtures thereof.

In one aspect, suitable Table 1 perfume raw materials include perfume raw materials from number 1 to number 29 and mixtures thereof.

In one aspect, suitable perfume raw materials having boiling point less than or equal to 250° C. and a ClogP greater than 2.5 are those materials listed in Table 2 below and such materials are defined as Table 2 perfume raw materials.

TABLE 2 Perfumes Number Registry Name Trade Name 1 Bicyclo[2.2.1]heptane, 2,2-dimethyl-3- Camphene methylene- 2 Bicyclo[3.1.1]heptane, 6,6-dimethyl-2- Beta Pinene methylene-, (1S)- 3 Bicyclo[3.1.1]hept-2-ene, 2,6,6- Alpha Pinene trimethyl- 4 Propanoic acid, pentyl ester Amyl Propionate 5 1,6-Octadiene, 7-methyl-3-methylene- Myrcene 6 Cyclohexene, 1-methyl-4-(1- Dipentene methylethenyl)- 7 Cyclohexene, 1-methyl-4-(1- Terpineolene methylethenyl)- 8 Acetic acid, hexyl ester Hexyl Acetate 9 Cyclohexene, 1-methyl-4-(1- Terpineolene methylethylidene)- 10 Benzene, 1-methoxy-4-methyl- Para Cresyl Methyl Ether 11 1-Octen-3-ol, acetate Amyl Vinyl Carbinyl Acetate 12 Octanal Octyl Aldehyde 13 2-Oxabicyclo[2.2.2]octane, 1,3,3- Eucalyptol trimethyl- 14 Butanoic acid, pentyl ester Amyl Butyrate 15 Heptanoic acid, ethyl ester Ethyl Oenanthate 16 5-Heptenal, 2,6-dimethyl- Melonal 17 Hexanoic acid, 2-propenyl ester Allyl Caproate 18 3-Cyclohexene-1-carboxaldehyde, Ligustral dimethyl- 19 3-Hexene, 1-(1-ethoxyethoxy)-, (Z)- Leaf Acetal 20 Octanal, 3,7-dimethyl- Dihydrocitronellal 21 2-Octynoic acid, methyl ester Methyl Heptine Carbonate 22 2-Nonenal 2 Nonen-1-al 23 1,6-Octadien-3-ol, 3,7-dimethyl- Linalool 24 Benzoic acid, ethyl ester Ethyl Benzoate 25 6-Octenal, 3,7-dimethyl- Citronellal 26 Cyclohexanol, 1-methyl-4-(1- Dihydroterpineol methylethyl)- 27 1-Hexanol, 3,5,5-trimethyl-, acetate Iso Nonyl Acetate 28 3,5-Octadien-2-ol, 2,6-dimethyl-, (?,Z)- Muguol 29 Cyclohexanone, 5-methyl-2-(1- Iso Menthone methylethyl)-, cis- 30 Heptanoic acid, 2-propenyl ester Allyl Heptoate 31 Butanoic acid, 3-hexenyl ester, (Z)- Cis 3 Hexenyl Butyrate 32 1,6-Octadien-3-ol, 3,7-dimethyl-, Linalyl Formate formate 33 3-Cyclohexen-1-ol, 4-methyl-1-(1- Terpinenol methylethyl)- 34 Bicyclo[2.2.1]heptan-2-ol, 1,3,3- Fenchyl Alcohol trimethyl- 35 Cyclohexanol, 2-(1,1-dimethylethyl)-, Verdol cis- 36 3-Octanol, 3,7-dimethyl-, acetate Tetrahydro Linayl Acetate 37 Bicyclo[2.2.1]heptan-2-ol, 1,7,7- Borneol Crystals trimethyl-, (1S-endo)- 38 Decanal Decyl Aldehyde 39 3-Cyclohexene-1-methanol, Alpha Terpineol .alpha.,.alpha.,4-trimethyl- 40 Cyclohexanol, 5-methyl-2-(1- Menthol methylethyl)- 41 3-Cyclohexene-1-carboxaldehyde, Iso Cyclo Citral 2,4,6-trimethyl- 42 7-Octen-2-ol, 2,6-dimethyl-, acetate Dihydro Terpinyl Acetate 43 2H-Pyran-2-one, 6-butyltetrahydro- Nonalactone 44 3-Hepten-2-one, 3,4,5,6,6-pentamethyl- Koavone 45 1,6-Nonadien-3-ol, 3,7-dimethyl- Ethyl Linalool 46 4-Decenal, (E)- Decenal (Trans-4) 47 Terpineol Terpineol 48 7-Octen-2-ol, 2-methyl-6-methylene-, Myrcenyl Acetate acetate 49 2-Butenoic acid, 2-methyl-, 3-hexenyl Cis-3-Hexenyl Tiglate ester, (E,Z)- 50 1,6-Octadien-3-ol, 3,7-dimethyl-, Linalyl Acetate acetate 51 Benzene, 1-methoxy-4-(1-propenyl)-, Anethol Usp (E)- 52 2-Decenal 2 Decene-1-al 53 2,6-Octadienal, 3,7-dimethyl- Citral 54 6-Octen-1-ol, 3,7-dimethyl-, formate Citronellyl Formate 55 Cyclopentanone, 3-methyl-2-pentyl- Jasmylone 56 Undecenal Iso C-11 Aldehyde 57 6-Octen-1-ol, 3,7-dimethyl- Citronellol 58 Cyclohexanemethanol, Dihydro Terpinyl Acetate .alpha.,.alpha.,4-trimethyl-, acetate 59 3-Cyclohexene-1-methanol, Terpinyl Acetate .alpha.,.alpha.,4-trimethyl-, acetate 60 2,6-Octadien-1-ol, 3,7-dimethyl-, Geranyl Formate formate, (E)- 61 Bicyclo[2.2.1]heptan-2-ol, 1,3,3- Fenchyl Acetate trimethyl-, acetate 62 Bicyclo[2.2.1]heptan-2-ol, 1,7,7- Iso Bornyl Acetate trimethyl-, acetate, exo- 63 2,6-Octadien-1-ol, 3,7-dimethyl-, (E)- Geraniol 64 2,6-Octadien-1-ol, 3,7-dimethyl-, (Z)- Nerol 65 Cyclohexanol, 2-(1,1-dimethylethyl)-, Verdox acetate 66 Undecanal, 2-methyl- Methyl Nonyl Acetaldehyde 67 Undecanal Undecyl Aldehyde 68 2H-Pyran-2-one, tetrahydro-6-pentyl- Delta Decalactone 69 6-Octen-1-ol, 3,7-dimethyl-, acetate Citronellyl Acetate 70 10-Undecenal Intreleven Aldehyde Sp 71 2(3H)-Furanone, 5-hexyldihydro- Gamma Decalactone 72 2,6-Octadien-1-ol, 3,7-dimethyl-, Geranyl Acetate acetate, (E)- 73 2H-Pyran-2-one, tetrahydro-6-(3- Jasmolactone pentenyl)- 74 Cyclohexanol, 5-methyl-2-(1- Menthyl Acetate methylethyl)-, acetate, (1.alpha.,2.beta.,5.alpha.)- 75 2-Undecenal 2-Undecene-1-Al 76 2H-Pyran-2-one, tetrahydro-6-(2- Jasmolactone pentenyl)-, (Z)- 77 2,6-Octadien-1-ol, 3,7-dimethyl-, Neryl Acetate acetate, (Z)- 78 Benzeneethanol, .alpha.,.alpha.- Dimethyl Benzyl Carbinyl Acetate dimethyl-, acetate 79 4,9-Decadienal, 4,8-dimethyl- Floral Super 80 3-Octanol Octanol-3 81 2-Heptanol, 2,6-dimethyl- Dimethyl-2,6-Heptan-2-ol 82 Propanoic acid, 2-methyl-, 1,3- Iso Pentyrate dimethyl-3-butenyl ester 83 3-Nonanone Ethyl Hexyl Ketone 84 2,4,6-Octatriene, 2,6-dimethyl- Allo-Ocimene 85 Bicyclo[2.2.1]heptane, 2-ethyl-5- Neoproxen methoxy- 86 1-Octanol Octyl Alcohol 87 3-Octanol, 3,7-dimethyl- Linacsol 88 Propanoic acid, 2-methyl-, 3-hexenyl Verdural B Extra ester, (Z)- 89 2H-Pyran, tetrahydro-4-methyl-2-(2- Methyl Iso Butenyl Tetrahydro Pyran methyl-1-propenyl)- 90 Nonanal Nonyl Aldehyde 91 Hexanoic acid, 2-methylpropyl ester Iso Butyl Caproate 92 Cyclohexane, 3-ethoxy-1,1,5-trimethyl- Herbavert 93 7-Octen-2-ol, 2-methyl-6-methylene-, Dihydro Myrcenol dihydro deriv. 94 Ethanone, 1-(3,3-dimethylcyclohexyl)- Herbac 95 Propanoic acid, 2,2-dimethyl-, hexyl Hexyl Neo Pentanoate ester 96 3-Heptanone, 5-methyl-, oxime Stemone 97 Isononanol Iso Nonyl Alcohol 98 Cyclohexanone, 2-(1-methylpropyl)- 2-Sec-Butyl Cyclo Hexanone 99 Butanoic acid, 2-methyl-, hexyl ester Hexyl-2-Methyl Butyrate 100 1-Nonanol Nonyl Alcohol 101 Cyclohexaneethanol, acetate Cyclohexyl Ethyl Acetate 102 1-Octanol, 3,7-dimethyl- Dimethyl Octanol 103 Cyclopentanone, 2-pentyl- Delphone 104 Cyclohexanemethanol, 4-(1- Mayol methylethyl)-, cis- 105 6-Octen-1-ol, 3,7-dimethyl-, (S)- Baranol 106 Benzaldehyde, 4-(1-methylethyl)- Cuminic Aldehyde 107 Propanoic acid, 2-methyl-, Benzyl Iso Butyrate phenylmethyl ester 108 Propanoic acid, 2-methyl-, 4- Para Cresyl Iso Butyrate methylphenyl ester 109 Carbonic acid, 4-cycloocten-1-yl Violiff methyl ester 110 1,6-Octadien-3-ol, 3,7-dimethyl-, Linalyl Propionate propanoate 111 Cyclohexanemethanol, .alpha.-methyl- Mugetanol 4-(1-methylethyl)- 112 Butanoic acid, phenylmethyl ester Benzyl Butyrate 113 4,7-Methano-1H-inden-5-ol, octahydro-, Dihydro Cyclacet acetate 114 2-Cyclopenten-1-one, 3-methyl-2- Dihydrojasmone pentyl- 115 Bicyclo[2.2.1]heptan-2-ol, 1,7,7- Iso Bornyl Propionate trimethyl-, propanoate, exo- 116 2,6-Octadienenitrile, 3,7-dimethyl- Geranyl Nitrile 117 Benzene, ethenyl- Styrene 118 Benzene, methyl(1-methylethyl)- Cymene Coeur 119 Cyclohexanol, 3,3,5-trimethyl-, cis- Trimethylcyclohexanol 120 1-Hexanol, 5-methyl-2-(1- Tetrahydro Lavandulol methylethyl)-, (R)- 121 Cyclohexanol, 4-(1-methylethyl)- Roselea 122 7-Octen-2-ol, 2,6-dimethyl-, formate Dimyrcetol 123 Cyclohexanone, 5-methyl-2-(1- Menthone Racemic methylethyl)-, trans- 124 1,3,5-Undecatriene Galbanolene Super 125 5,7-Octadien-2-ol, 2,6-dimethyl- Ocimenol 126 2-Cyclohexene-1-carboxylic acid, Methyl Cyclogeranate 2,6,6-trimethyl-, methyl ester 127 Benzene, (2-bromoethenyl)- Brom Styrol 128 Benzene, 1-methoxy-4-(2-propenyl)- Methyl Chavicol 129 2H-Pyran, 6-butyl-3,6-dihydro-2,4- Gyrane dimethyl- 130 Cyclohexanemethanol, .alpha.,3,3- Aphermate trimethyl-, formate 131 Cyclohexanol, 4-(1,1-dimethylethyl)- Patchon 132 Cyclohexanol, 5-methyl-2-(1- Menthol Natural methylethyl)-, [1R- (1.alpha.,2.beta.,5.alpha.)]- 133 1,3-Dioxane, 2-butyl-4,4,6-trimethyl- Herboxane 134 2-Nonynoic acid, methyl ester Methyl Octine Carbonate 135 6-Octenenitrile, 3,7-dimethyl- Baranyl Nitrile 136 Decanal, 2-methyl- Methyl Octyl Acetaldehyde 137 2-Nonanol, 6,8-dimethyl- Nonadyl 138 Phenol, 4-(1,1-dimethylethyl)- Para Tertiary Butyl Phenol 139 1-Hexanol, 5-methyl-2-(1- Tetrahydro Lavandulyl Acetate methylethyl)-, acetate 140 Cyclohexanol, 5-methyl-2-(1- Iso Pulegol methylethenyl)-, [1R- (1.alpha.,2.beta.,5.alpha.)]- 141 Cyclohexanone, 4-(1,1- Orivone dimethylpropyl)- 142 2-Undecanone Methyl Nonyl Ketone 143 Cyclohexanemethanol, .alpha.,3,3- Rosamusk trimethyl-, acetate 144 3-Cyclohexene-1-methanol, 2,4,6- Isocyclogeraniol trimethyl- 145 2,6-Octadiene, 1,1-dimethoxy-3,7- Citral Dimethyl Acetal dimethyl- 146 1-Decanol Rhodalione 147 2-Cyclohexen-1-one, 3-methyl-5- Livescone propyl- 148 Phenol, 2-methyl-5-(1-methylethyl)- Carvacrol 149 2-Naphthalenol, decahydro- Trans Deca Hydro Beta Naphthol 150 Cyclohexanol, 4-(1,1-dimethylethyl)-, Tertiary Butyl Cyclohexyl Acetate acetate 151 9-Decen-1-ol Rosalva 152 Phenol, 5-methyl-2-(1-methylethyl)- Thymol Nf 153 Cyclohexanol, 5-methyl-2-(1- Iso Pulegol Acetate methylethenyl)-, acetate, [1R- (1.alpha.,2.beta.,5.alpha.)]- 154 Benzene, [(3-methylbutoxy)methyl]- Iso Amyl Benzyl Ether 155 2(3H)-Furanone, 5-hexyldihydro-5- Lactojasmon methyl- 156 Benzoic acid, butyl ester Butyl Benzoate 157 Bicyclo[3.2.1]octan-8-one, 1,5- Buccoxime dimethyl-, oxime 158 2-Cyclopenten-1-one, 2-methyl-3-(2- Iso Jasmone pentenyl)-

In one aspect, suitable Table 2 perfume raw materials include perfume raw materials from number 1 to number 116 and mixtures thereof.

In one aspect, suitable Table 2 perfume raw materials include perfume raw materials from number 1 to number 79 and mixtures thereof.

In one aspect, suitable perfume raw materials having boiling point greater than 250° C. but less than or equal to 280° C. are those materials listed in Table 3 below and such materials are defined as Table 3 perfume raw materials.

TABLE 3 Perfumes Number Registry Name Trade Name 1 Dodecanenitrile Clonal 2 Cyclohexanepropanoic acid, 2-propenyl ester Allyl Cyclohexane Propionate 3 2-Buten-1-one, 1-(2,6,6-trimethyl-2- Alpha Damascone cyclohexen-1-yl)- 4 1,4-Cyclohexanedicarboxylic acid, diethyl Fructalate ester 5 2(3H)-Furanone, 5-heptyldihydro- Undecalactone 6 Naphthalene, 2-methoxy- Beta Naphthol Methyl Ether 7 Benzenepropanal, 4-(1,1-dimethylethyl)- Bourgeonal 8 3-Cyclopentene-1-butanol, .beta.,2,2,3- Brahmanol tetramethyl- 9 1H-3a,7-Methanoazulen-6-ol, octahydro- Cedrol 3,6,8,8-tetramethyl-,[3R- (3.alpha.,3a.beta.,6.alpha.,7.beta.,8a.alpha.)]- 10 2-Propen-1-ol, 3-phenyl-, acetate Cinnamyl Acetate 11 Benzenepropanal, .alpha.-methyl-4-(1- Cymal methylethyl)- 12 2-Buten-1-one, 1-(2,6,6-trimethyl-1- Damascone Beta cyclohexen-1-yl)-, (Z)- 13 2-Buten-1-one, 1-(2,6,6-trimethyl-1,3- Damascenone cyclohexadien-1-yl)- 14 2-Buten-1-one, 1-(2,6,6-trimethyl-3- Delta Damascone cyclohexen-1-yl)- 15 Butanoic acid, 1,1-dimethyl-2-phenylethyl Dimethyl Benzyl Carbinyl ester Butyrate 16 2-Dodecenal 2 Dodecene-1-al 17 2H-Pyran-2-one, 6-heptyltetrahydro- Dodecalactone 18 Oxiranecarboxylic acid, 3-methyl-3-phenyl-, Ethyl Methyl Phenyl Glycidate ethyl ester 19 Oxiranecarboxylic acid, 3-phenyl-, ethyl Ethyl Phenyl Glycidate ester 20 Phenol, 2-methoxy-4-(2-propenyl)- Eugenol 21 Benzenepropanal, .beta.-methyl-3-(1- Florhydral methylethyl)- 22 Benzenepropanal, 2-ethyl-.alpha.,.alpha.- Floralozone dimethyl- 23 4,7-Methano-1H-inden-6-ol, 3a,4,5,6,7,7a- Frutene hexahydro-, propanoate 24 2,6-Octadienenitrile, 3,7-dimethyl-, (E)- Geranyl Nitrile 25 1,3-Benzodioxole-5-carboxaldehyde Heliotropin 26 Ionone Ionone Ab 27 3-Buten-2-one, 4-(2,6,6-trimethyl-2- Ionone Alpha cyclohexen-1-yl)-, (E)- 28 3-Buten-2-one, 4-(2,6,6-trimethyl-1- Ionone Beta cyclohexen-1-yl)- 29 3-Buten-2-one, 4-(2,6,6-trimethyl-1- Ionone Beta cyclohexen-1-yl)-, (E)- 30 3-Buten-2-one, 3-methyl-4-(2,6,6-trimethyl- Ionone Gamma Methyl 2-cyclohexen-1-yl)- 31 2-Buten-1-one, 1-(2,4,4-trimethyl-2- Isodamascone N cyclohexen-1-yl)-, (E)- 32 Phenol, 2-methoxy-4-(1-propenyl)- Iso Eugenol 33 2H-Pyran-4-ol, tetrahydro-3-pentyl-, acetate Jasmal 34 Bicyclo[3.1.1]hept-2-ene-2-ethanol, 6,6- Nopyl Acetate dimethyl-, acetate 35 Benzenepropanol, .alpha.,.alpha.-dimethyl-, Phenyl Ethyl Dimethyl acetate Carbinyl Acetate 36 Propanoic acid, 2-methyl-, 3a,4,5,6,7,7a- Cyclabute hexahydro-4,7-methano-1H- 37 Benzaldehyde, 4-hydroxy-3-methoxy- Vanillin 38 3-Cyclohexene-1-carboxaldehyde, 1-methyl- Vernaldehyde 4-(4-methylpentyl)- 39 Benzenemethanol, ar-methoxy-, acetate Anisyl Acetate 40 Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, Herbanate Ci 3-(1-methylethyl)-,ethyl ester, (2-endo,3- exo)- 41 Butanoic acid, 3-methyl-, 2-phenylethyl ester Beta Phenyl Ethyl Isovalerate 42 Benzenepropanal, 4-methoxy-.alpha.-methyl- Canthoxal 43 Bicyclo[7.2.0]undec-4-ene, 4,11,11- Caryophyllene Extra trimethyl-8-methylene-,[1R-(1R*,4E,9S*)]- 44 Cyclohexenebutanal, .alpha.,2,2,6- Cetonal tetramethyl- 45 2-Propen-1-ol, 3-phenyl- Cinnamic Alcohol 46 6-Octen-1-ol, 3,7-dimethyl-, propanoate Citronellyl Propionate 47 Propanoic acid, decyl ester N-Decyl Propionate 48 Phenol, 2-methoxy-4-propyl- Dihydro Eugenol 49 Cyclohexanol, 1-ethenyl-2-(1-methylpropyl)-, Dihydro Ambrate acetate 50 2-Propenoic acid, 3-phenyl-, ethyl ester Ethyl Cinnamate 51 Butanoic acid, 3,7-dimethyl-2,6-octadienyl Geranyl Butyrate ester, (E)- 52 2-Octanol, 8,8-dimethoxy-2,6-dimethyl- Hydroxycitronellal Dimethyl Acetal 53 Cyclohexadieneethanol, 4-(1-methylethyl)-, Iso Bergamate formate 54 Dodecanal Lauric Aldehyde 55 Propanoic acid, 2-methyl-, 1-ethenyl-1,5- Linalyl Iso Butyrate dimethyl-4-hexenyl ester 56 Benzenepropanol, .beta.,.beta.,3-trimethyl- Majantol 57 Benzene, 1,2-dimethoxy-4-(2-propenyl)- Methyl Eugenol 58 Propanoic acid, 2-methyl-, 2-phenylethyl Phenyl Ethyl Iso Butyrate ester 59 2-Propenenitrile, 3-phenyl- Cinnamalva 60 Benzene, [2-(1-propoxyethoxy)ethyl]- Acetal R 61 9-Undecenal, 2,6,10-trimethyl- Adoxal 62 2-Naphthalenol, 1,2,3,4,4a,5,6,7-octahydro- Ambrinol 20t 2,5,5-trimethyl- 63 2-Naphthalenol, octahydro-2,5,5-trimethyl- Ambrinol 20t 64 Ethanol, 2-[(1,7,7- Arbanol trimethylbicyclo[2.2.1]hept-2-yl)oxy]-, exo- 65 1H-2-Benzopyran, 3,4,4a,5,8,8a(or Bigarade Oxide 3,4,4a,7,8,8a)-hexahydro-3,3,6,7- 66 Cyclohexene, 4-(1,5-dimethyl-4- Bisabolene hexenylidene)-1-methyl- 67 1H-3a,7-Methanoazulene, octahydro-6- Cedramber methoxy-3,6,8,8-tetramethyl-,[3R- (3.alpha.,3a.beta.,6.alpha.,7.beta.,8a.alpha.)]- 68 Phenol, 4-chloro-3,5-dimethyl- 4-Chloro 3,5 Xylenol 69 2,6-Octadiene, 1,1-diethoxy-3,7-dimethyl- Citrathal 70 Acetaldehyde, [(3,7-dimethyl-6- Citronellyl Oxyacetaldehyde octenyl)oxy]- 71 Benzenepropanenitrile, .alpha.-ethenyl- Citrowanil B .alpha.-methyl- 72 Cyclohexanol, 2-(1,1-dimethylpropyl)-, Coniferan acetate 73 2H-1-Benzopyran-2-one Coumarin 74 1,3-Nonanediol, monoacetate Diasmol 75 Benzene, 1,1′-methylenebis- Diphenyl Methane 76 Benzene, 1,1′-oxybis- Diphenyl Oxide 77 1,6-Octadiene, 3-(1-ethoxyethoxy)-3,7- Elinthal dimethyl- 78 Cyclopentanone, 2-heptyl- Fleuramone 79 5,8-Methano-2H-1-benzopyran-2-one, 6- Florex ethylideneoctahydro- 80 Octanoic acid, 2-acetyl-, ethyl ester Gelsone 81 Indeno[1,2-d]-1,3-dioxin, 4,4a,5,9b- Indoflor Crist. tetrahydro- 82 Benzeneacetic acid, 2-methylpropyl ester Iso Butyl Phenylacetate 83 2,6-Nonadienenitrile, 3,7-dimethyl- Lemonile 84 3-Decanone, 1-hydroxy- Methyl Lavender Ketone 85 Undecane, 1,1-dimethoxy-2-methyl- Methyl Nonyl Acetaldehyde Dimethyl Aceta 86 1-Propanone, 1-[2-methyl-5-(1-methylethyl)- Nerone 2-cyclohexen-1-yl]- 87 5,9-Undecadienal, 2,6,10-trimethyl- Oncidal 88 Quinoline, 6-methyl- Para Methyl Quinoline 89 Propanoic acid, 2-methyl-, 2-phenoxyethyl Phenoxy Ethyl Iso Butyrate ester 90 Ethanol, 2-phenoxy-, propanoate Phenoxy Ethyl Propionate Formerly N-225 91 4,7-Methano-1H-indene-2-carboxaldehyde, Scentenal octahydro-5-methoxy- 92 9-Undecen-2-one, 6,10-dimethyl- Tetra Hydro Psuedo Ionone 93 Benzenemethanol, .alpha.-(trichloromethyl)-, Trichloromethyl Phenyl acetate Carbinyl Acetate 94 Phenol, 2-methoxy-4-(methoxymethyl)- Vaniwhite 95 Bicyclo[2.2.2]oct-5-ene-2-carboxaldehyde, Maceal 6-methyl-8-(1-methylethyl)- 96 Benzene, [2-(3-methylbutoxy)ethyl]- Phenyl Ether Isamyl Ether (Aka Anther) 97 2-Cyclohexene-1-carboxylic acid, 2,3,6,6- Givescone tetramethyl-, ethyl ester

In one aspect, suitable Table 3 perfume raw materials include perfume raw materials from number 1 to number 58 and mixtures thereof.

In one aspect, suitable Table 3 perfume raw materials include perfume raw materials from number 1 to number 39 and mixtures thereof.

In one aspect, suitable perfume raw materials may be selected from the group consisting of 4-methoxybenzaldehyde; 4-phenylbutan-2-one; 3,7-dimethyl-2-methylene-6-octenal; 4-(2,6,6-trimethyl cyclohex-1-ene-1-yl) but-3-ene-2-one; 2,4-dimethylcyclohex-3-ene-1-carbaldehyde; 2-methyl-3-(para iso propylphenyl)propionaldehyde; 2-Buten-1-one, 1-(2,6,6-trimethyl-1,3-cyclohexadien-1-yl)-; 1-cyclohexyl-ethylene-crotonate; 1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-2-buten-1-one; 3-methyl cyclopentadecenone; 4-(2,6,6-trimethyl-1-cyclohexenyl)butan-2-one; 2,5-Dimethyl-2-octen-6-one; dihydro-nor-cyclopentadienyl acetate; 3-(o-(and p-)ethylphenyl)-2,2-dimethylpropionaldehyde; 3-(3-isopropylphenyl)butanal; 3-Buten-2-one, 3-methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-; alpha-methyl-3,4(methylenedioxy)hydrocinnamaldehyde; n-hexyl ortho hydroxy benzoate; 7-acetyl-1,2,3,4,5,6,7,8-octahydro-1,1,6,7,tetramethyl naphthalene; 4-(1-Ethoxyvinyl)-3,3,5,5-tetramethyl-cyclohexan-1-one; 2-Cyclohexen-1-one, 2-methyl-5-(1-methylethenyl)-, (R)-; 2,4-Dimethyl-3-cyclohexene-1-carboxaldehyde; 3,7-dimethyl-1,6-octadien-3-ol; 2,6-Dimethyl-5-Heptenal; Methyl Dihydro Jasmonate; Methyl Nonyl Acetaldehyde; 6,6-dimethoxy-2,5,5-trimethylhex-2-ene; 2-Cyclohexen-1-one, 2-methyl-5-(1-methylethenyl)-, (R)-; Octaldehyde; 2-Cyclohexyl-1,6-heptadien-3-one and mixtures thereof.

Suitable polymeric materials may comprise at least two moieties each of which may be independently selected from the group consisting of carboxylic acid, hydroxyl, ester, amide, amine, nitrile and thiol moieties.

In one aspect, said polymeric compound comprises, per polymeric compound, at least two moieties selected from the moieties consisting of a carboxylic acid moiety, an amine moiety, a hydroxyl moiety, and a nitrile moiety. In one aspect, the polymeric material contains two or more carboxylic acid moieties on each polymeric molecule. In one aspect, polymeric materials may contain a backbone of polybutadiene, polyisoprene, polybutadiene/styrene, polybutadiene/acrylonitrile, carboxyl-terminated polybutadiene/acrylonitrile or combinations thereof. In another aspect, suitable polymeric materials encompass amine terminated, epoxy terminated, or vinyl terminated polymers. Suitable molecular weights for these polymers range from about 1,000 to about 10,000,000. In one aspect, the suitable polymers may have molecular weights that range from about 1,000 to about 10,000,000 or from about 2,000 to about 50,000. Suitable polymeric materials are available from NOVEON (Cleveland, Ohio U.S.A) and SARTOMER (Philadelphia, Pa. U.S.A.). Such materials include HYCAR® materials CTB 2000x162, CTBNX 1300x18, CTBNX 1300x9, CTBN 1300x8, CTBN 1300x31, ATB 2000x173, ATBN 1300x21, ATBN 1300x16, ATBN 1300x45, ATBN 1300x35, ATBN 1300x42, VTB 2000x168, VTBNX1300x33, VTBNX1300x43, ETBN 1300x40, and ETBN 1300x44 from NOVEON or Emerald Performance Materials of Cuyahoga Falls, Ohio U.S.A. and Krasol® LBH 5000 from SARTOMER.

In one aspect, the benefit delivery composition may comprise a cross-linker. In any aspect, such cross-linker may provide covalent cross-linking and/or ionic cross-linking. In one aspect, the benefit agent delivery composition comprises a cross-linker at a concentration similar to the equivalence of the polymeric material. In one aspect, the equivalence ratio of cross-linker equivalence to the carboxylic acid equivalence within the composition is from about 0.5 to about 2.0. In one aspect, the equivalence ratio is from about 0.8 to about 1.2. The cross-linker can be any material that provides cross-linking when placed in the presence of the carboxylic acid containing polymer. Suitable cross-linkers include polyamines, expoxides and polycarbodiimides. In one aspect, the polycarbodiimide cross-linker compound may be ZOLDINE™ XL-29SE manufactured by Angus Chemical Company, a subsidiary of the Dow Chemical Company of Midland, Mich. U.S.A. In one aspect, polyamines may comprise diethylenetriamine, polyethyleneimines, polyvinylamines, and/or ethylene diamine moieties.

In one aspect, the crosslinker comprises a polyamine that may comprise diethylenetriamine, ethylene diamine, polyethyleneimine, polyvinylamine, bis(3-aminopropyl)piperazine, N,N-Bis-(3-aminopropyl)methylamine, tris(2-aminoethyl)amine or mixtures thereof.

Suitable polyamines include Lupasolg WF, SK, PS, PO100, P, HF, G500, G35, G20 water free, G20, G100, FG, FC, and PR8515 products supplied by BASF of Ludwigshaven, Germany.

Other materials may be added to the benefit agent delivery compositions disclosed herein. For example, colorants can be added to such benefit agent delivery compositions including dyes and pigments. The colorant may be one or more oil soluble dyes. Such dyes may be added to the benefit agent prior to the formation of the benefit agent delivery compositions disclosed herein. Antioxidants may be added to benefit agent delivery compositions disclosed herein. Such antioxidants may protect benefit agents, including fragrances from oxidation. Suitable antioxidants include BHA supplied by Eastman Chemical Company of Kingsport Tenn. U.S.A. UV inhibitors can be added to benefit agent delivery compositions disclosed herein and may prevent discoloration. Suitable UV inhibitors include TINUVIN® commercial products supplied by Ciba® of Basel, Switzerland.

Other materials maybe added to the benefit agent delivery compositions disclosed herein are materials that will help to process the benefit agent delivery compositions like solvents, diluents, surfactants, fatty acids, polymers, suitable materials are diluents like benzylbenzoate, nonionic surfactants like TAE80, fatty acids like coconut oil, polymers like PEG4000.

In one aspect, the benefit agent delivery compositions of the present invention may be clear. However, such compositions may also be opaque. Such compositions can be made opaque by the addition of opacifying agents. Suitable opacifying agents include titanium dioxide, zinc oxide, inorganic salts, waxes, water, and other organic opacifiers that are well known to those of skilled in the art.

Additional materials may be added to the benefit agent delivery compositions disclosed herein. Such materials may or may not be volatile. Such materials include solvents, oils, esters, phthalates, fatty acids, triglycerides, ethers, oils, aliphatic materials, hydrocarbons, plasticizers, and alcohols. Such materials may or may not be hydrophilic. Suitable hydrophilic materials include water, glycols, and alcohols. In one aspect, surfactants may be added to the benefit agent delivery compositions disclosed herein. Suitable surfactants include nonionic, anionic, cationic, and amphoteric surfactants--examples of which will be well known to those of skill in the art. The inclusion of surfactants may facilitate the inclusion of hydrophilic materials into the benefit agent delivery compositions disclosed herein.

Process of Making Benefit Agent Delivery Compositions

The benefit agent delivery compositions disclosed in the present application may be made via the teachings of USPA 2006/0067963 A1, and the examples disclosed herein.

The benefit agent containing compositions disclosed in the present application may be processed in accordance with the teachings of U.S. Pat. Nos. 6,451,751 B1, 6,972,276 B1, 6,764,986 B1, 6,740,713 B1 and the examples disclosed herein. Suitable forms for such benefit agent delivery compositions include, solids and fluids including agglomerates, emulsions, solutions, prills, beads and encapsulates. When employed to product a benefit agent delivery composition the particle size of the benefit agent delivery composition in said agglomerates, emulsions, solutions, prills, beads and encapsulates may be from about 0.1 microns to about 100 microns, from about 1 micron to about 60 microns or even from about 5 to about 40 microns. In addition to the foregoing, the benefit agent delivery compositions of the present invention may be further processed in accordance with the teachings of published US Patent Application No. 2007/0196502 A1 to yield a particle wherein the benefit agent delivery composition comprises at least a portion or even all of one or more layers of the resulting particle.

In one aspect, a method for making a benefit agent delivery composition comprising:

    • a.) mixing a first mixture, wherein said first mixture comprises: from about 15% to about 95% by weight of a volatile hydrophobic liquid; and from about 3% to about 40% by weight of a polymeric compound containing a carboxylic acid, until said first mixture is completely mixed; and mixing into said first mixture, from about 1.5% to about 40% by weight of a cross-linking agent; or
    • b.) mixing a first mixture, wherein said first mixture comprises: from about 15% to about 95% by weight of a volatile hydrophobic liquid; and from about 3% to about 40% by weight of a polymeric compound containing a carboxylic acid, until said first mixture is completely mixed; and mixing into said first mixture, from about 0% to about 40% by weight of a cross-linking agent; or
    • c.) mixing a first mixture, wherein said first mixture comprises: from about 15% to about 95% by weight of a volatile hydrophobic liquid; and from about 3% to about 40% by weight of a polymeric compound containing a carboxylic acid, until said first mixture is completely mixed; and mixing into said first mixture a second mixture, wherein said second mixture comprises: from 15% to about 95% by weight volatile hydrophobic liquid; and from about 1.5% to about 40% by weight of a cross-linking agent; or
    • d.) combining from about 15% to about 95% by weight of a volatile hydrophobic liquid; and from about 3% to about 40% by weight of a polymeric compound containing a carboxylic acid, until said first mixture is completely mixed; and mixing into said first mixture, from about 0% to about 40% by weight of a cross-linking agent;
    • e.) optionally combining the mixtures produced in a.), b.), c.) and/or d.) with a diluent and/or a surfactant; and/or further processing the mixtures produced in a.), b.), c.) and/or d.) to form a particle, bead and/or agglomerate is disclosed.

In one aspect, the benefit agent delivery composition is pre-made and added to a consumer.

In one aspect the components of the benefit agent delivery composition are added separately to a consumer product and the benefit agent delivery composition may form in the consumer before, during and/or after use by the consumer.

In one aspect, when additional benefit agent(s) and/or benefit agent delivery system(s), for example perfume and/or encapsulated perfume, are employed to form a particle, bead and/or agglomerate, the benefit agent delivery composition of the present invention may be added before, during or after said additional benefit agent(s) and/or benefit agent delivery system(s) are added to said a particle, bead and/or agglomerate.

In one aspect, when additional benefit agent(s) and/or benefit agent delivery system(s), for example perfume and/or encapsulated perfume, are employed, the benefit agent delivery composition of the present invention may be added before, during or after said additional benefit agent(s) and/or benefit agent delivery system(s) are added to a consumer.

Suitable equipment for use in the processes disclosed herein may include continuous stirred tank reactors, homogenizers, turbine agitators, recirculating pumps, paddle mixers, ploughshear mixers, ribbon blenders, vertical axis granulators, twin screw extruders and drum mixers, both in batch and, where available, in continuous process configurations, spray dryers, and extruders. Such equipment can be obtained from Lodige GmbH (Paderbom, Germany), Littleford Day, Inc. (Florence, Ky., U.S.A.), Forberg A S (Larvik, Norway), Glatt Ingenieurtechnik GmbH (Weimar, Germany), Niro (Soeborg, Denmark), Hosokawa Bepex Corp. (Minneapolis, Minn., USA), Arde Barinco (New Jersey, USA), Wenger (Sabetha, Kans. USA).

Compositions Comprising Benefit Agent Delivery Compositions

Applicants' compositions comprise an embodiment of the benefit agent delivery compositions disclosed in the present application. In one aspect, such compositions may be a consumer product. While the precise level of benefit agent delivery composition that is employed depends on the type and end use of the product comprising such composition, a products, including cleaning and/or fabric treatment products, may comprise, based on total product weight, from about 0.001% to about 25%, from about 0.01% to about 5%, or even from about 0.05% to about 3% benefit agent delivery composition.

In one aspect, a consumer product comprising at least one embodiment of a benefit agent delivery composition disclosed herein and a material selected from the group consisting of a surfactant, an enzyme, a polymer, a dye, a neat perfume, a perfume delivery system in addition to Applicants' benefit agent delivery system and mixtures thereof is disclosed. Suitable perfume delivery systems are described in published U.S. Patent Application No. 2007/0275866 A1

Aspects of the invention include the use of the benefit agent delivery compositions of the present invention in laundry detergent compositions (e.g., TIDE™), hard surface cleaners (e.g., MR CLEAN™), automatic dishwashing liquids (e.g., CASCADE™), dishwashing liquids (e.g., DAWN™), and floor cleaners (e.g., SWIFFER™). Non-limiting examples of cleaning compositions may include those described in U.S. Pat. Nos. 4,515,705; 4,537,706; 4,537,707; 4,550,862; 4,561,998; 4,597,898; 4,968,451; 5,565,145; 5,929,022; 6,294,514; 6,376,445, 7,169,741 B2 and U.S. Pat. No. 7,297,674 B2 as well as in U.S. Patent Application Publication No. 2005/0130864 A1. The cleaning compositions disclosed herein may be formulated such that, during use in aqueous cleaning operations, the wash water will have a pH of between about 5 and about 12, or between about 7.5 and 10.5. Liquid dishwashing product formulations typically have a pH between about 6.8 and about 9.0. Cleaning products are typically formulated to have a pH of from about 7 to about 12. Techniques for controlling pH at recommended usage levels include the use of buffers, alkalis, acids, etc., and are well known to those skilled in the art.

Fabric treatment compositions disclosed herein typically comprise a fabric softening active (“FSA”). Suitable fabric softening actives, include, but are not limited to, materials selected from the group consisting of quats, amines, fatty esters, sucrose esters, silicones, dispersible polyolefins, clays, polysaccharides, fatty oils, polymer latexes and mixtures thereof.

Adjunct Materials

While not essential for the purposes of the present invention, the non-limiting list of adjuncts illustrated hereinafter are suitable for use in the instant compositions and may be desirably incorporated in certain embodiments of the invention, for example to assist or enhance performance, for treatment of the substrate to be cleaned, or to modify the aesthetics of the composition as is the case with perfumes, colorants, dyes or the like. It is understood that such adjuncts are in addition to the components that are supplied via Applicants' delivery particles and FSAs. The precise nature of these additional components, and levels of incorporation thereof, will depend on the physical form of the composition and the nature of the operation for which it is to be used. Suitable adjunct materials include, but are not limited to, surfactants, builders, chelating agents, dye transfer inhibiting agents, dispersants, enzymes, and enzyme stabilizers, catalytic materials, bleach activators, polymeric dispersing agents, clay soil removal/anti-redeposition agents, brighteners, suds suppressors, dyes, additional perfume and perfume delivery systems, structure elasticizing agents, thickeners/structurants, fabric softeners, carriers, hydrotropes, processing aids and/or pigments. In addition to the disclosure below, suitable examples of such other adjuncts and levels of use are found in U.S. Pat. Nos. 5,576,282, 6,306,812 B1 and 6,326,348 B1 that are incorporated by reference.

As stated, the adjunct ingredients are not essential to Applicants' cleaning and fabric care compositions. Thus, certain embodiments of Applicants' compositions do not contain one or more of the following adjuncts materials: bleach activators, surfactants, builders, chelating agents, dye transfer inhibiting agents, dispersants, enzymes, and enzyme stabilizers, catalytic metal complexes, polymeric dispersing agents, clay and soil removal/anti-redeposition agents, brighteners, suds suppressors, dyes, additional perfumes and perfume delivery systems, structure elasticizing agents, thickeners/structurants, fabric softeners, carriers, hydrotropes, processing aids and/or pigments. However, when one or more adjuncts is present, such one or more adjuncts may be present as detailed below:

Surfactants—The compositions according to the present invention can comprise a surfactant or surfactant system wherein the surfactant can be selected from nonionic and/or anionic and/or cationic surfactants and/or ampholytic and/or zwitterionic and/or semi-polar nonionic surfactants. The surfactant is typically present at a level of from about 0.1%, from about 1%, or even from about 5% by weight of the cleaning compositions to about 99.9%, to about 80%, to about 35%, or even to about 30% by weight of the cleaning compositions.

Builders—The compositions of the present invention can comprise one or more detergent builders or builder systems. When present, the compositions will typically comprise at least about 1% builder, or from about 5% or 10% to about 80%, 50%, or even 30% by weight, of said builder. Builders include, but are not limited to, the alkali metal, ammonium and alkanolammonium salts of polyphosphates, alkali metal silicates, alkaline earth and alkali metal carbonates, aluminosilicate builders polycarboxylate compounds. ether hydroxypolycarboxylates, copolymers of maleic anhydride with ethylene or vinyl methyl ether, 1,3,5-trihydroxybenzene-2,4,6-trisulphonic acid, and carboxymethyl-oxysuccinic acid, the various alkali metal, ammonium and substituted ammonium salts of polyacetic acids such as ethylenediamine tetraacetic acid and nitrilotriacetic acid, as well as polycarboxylates such as mellitic acid, succinic acid, oxydisuccinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid, carboxymethyloxysuccinic acid, and soluble salts thereof.

Chelating Agents—The compositions herein may also optionally contain one or more copper, iron and/or manganese chelating agents. If utilized, chelating agents will generally comprise from about 0.1% by weight of the compositions herein to about 15%, or even from about 3.0% to about 15% by weight of the compositions herein.

Dye Transfer Inhibiting Agents—The compositions of the present invention may also include one or more dye transfer inhibiting agents. Suitable polymeric dye transfer inhibiting agents include, but are not limited to, polyvinylpyrrolidone polymers, polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinyloxazolidones and polyvinylimidazoles or mixtures thereof. When present in the compositions herein, the dye transfer inhibiting agents are present at levels from about 0.0001%, from about 0.01%, from about 0.05% by weight of the cleaning compositions to about 10%, about 2%, or even about 1% by weight of the cleaning compositions.

Dispersants—The compositions of the present invention can also contain dispersants. Suitable water-soluble organic materials are the homo- or co-polymeric acids or their salts, in which the polycarboxylic acid may comprise at least two carboxyl radicals separated from each other by not more than two carbon atoms.

Enzymes—The compositions can comprise one or more detergent enzymes which provide cleaning performance and/or fabric care benefits. Examples of suitable enzymes include, but are not limited to, hemicellulases, peroxidases, proteases, cellulases, xylanases, lipases, phospholipases, esterases, cutinases, pectinases, keratanases, reductases, oxidases, phenoloxidases, lipoxygenases, ligninases, pullulanases, tannases, pentosanases, malanases, B-glucanases, arabinosidases, hyaluronidase, chondroitinase, laccase, and amylases, or mixtures thereof. A typical combination is a cocktail of conventional applicable enzymes like protease, lipase, cutinase and/or cellulase in conjunction with amylase.

Enzyme Stabilizers—Enzymes for use in compositions, for example, detergents can be stabilized by various techniques. The enzymes employed herein can be stabilized by the presence of water-soluble sources of calcium and/or magnesium ions in the finished compositions that provide such ions to the enzymes.

Catalytic Metal Complexes—Applicants' compositions may include catalytic metal complexes. One type of metal-containing bleach catalyst is a catalyst system comprising a transition metal cation of defined bleach catalytic activity, such as copper, iron, titanium, ruthenium, tungsten, molybdenum, or manganese cations, an auxiliary metal cation having little or no bleach catalytic activity, such as zinc or aluminum cations, and a sequestrate having defined stability constants for the catalytic and auxiliary metal cations, particularly ethylenediaminetetraacetic acid, ethylenediaminetetra (methyl-enephosphonic acid) and water-soluble salts thereof. Such catalysts are disclosed in U.S. Pat. No. 4,430,243.

If desired, the compositions herein can be catalyzed by means of a manganese compound. Such compounds and levels of use are well known in the art and include, for example, the manganese-based catalysts disclosed in U.S. Pat. No. 5,576,282.

Cobalt bleach catalysts useful herein are known, and are described, for example, in U.S. Pat. Nos. 5,597,936 and 5,595,967. Such cobalt catalysts are readily prepared by known procedures, such as taught for example in U.S. Pat. Nos. 5,597,936, and 5,595,967.

Compositions herein may also suitably include a transition metal complex of a macropolycyclic rigid ligand—abreviated as “MRL”. As a practical matter, and not by way of limitation, the compositions and cleaning processes herein can be adjusted to provide on the order of at least one part per hundred million of the benefit agent MRL species in the aqueous washing medium, and may provide from about 0.005 ppm to about 25 ppm, from about 0.05 ppm to about 10 ppm, or even from about 0.1 ppm to about 5 ppm, of the MRL in the wash liquor.

Suitable transition-metals in the instant transition-metal bleach catalyst include manganese, iron and chromium. Suitable MRL's herein are a special type of ultra-rigid ligand that is cross-bridged such as 5,12-diethyl-1,5,8,12-tetraazabicyclo[6.6.2]hexa-decane.

Suitable transition metal MRLs are readily prepared by known procedures, such as taught for example in WO 00/32601, and U.S. Pat. No. 6,225,464.

Suitable thickeners/structurants and useful levels of same are described in U.S. Patent Application Publication No. 2005/0130864 A1 and U.S. Pat. Nos. 7,169,741 B2 and 7,297,674 B2.

Processes of Making and Using Compositions

The compositions of the present invention can be formulated into any suitable form and prepared by any process chosen by the formulator, non-limiting examples of which are described in U.S. Pat. No. 5,879,584; U.S. Pat. No. 5,691,297; U.S. Pat. No. 5,574,005; U.S. Pat. No. 5,569,645; U.S. Pat. No. 5,565,422; U.S. Pat. No. 5,516,448; U.S. Pat. No. 5,489,392; U.S. Pat. No. 5,486,303 all of which are incorporated herein by reference.

Method of Use

Compositions containing the benefit agent delivery composition disclosed herein can be used to clean or treat a situs inter alia a surface or fabric. Typically at least a portion of the situs is contacted with an embodiment of Applicants' composition, in neat form or diluted in a liquor, for example, a wash liquor and then the situs may be optionally washed and/or rinsed. In one aspect, a situs is optionally washed and/or rinsed, contacted with a particle according to the present invention or composition comprising said particle and then optionally washed and/or rinsed. For purposes of the present invention, washing includes but is not limited to, scrubbing, and mechanical agitation. The fabric may comprise most any fabric capable of being laundered or treated in normal consumer use conditions. Liquors that may comprise the disclosed compositions may have a pH of from about 3 to about 11.5. Such compositions are typically employed at concentrations of from about 500 ppm to about 15,000 ppm in solution. When the wash solvent is water, the water temperature typically ranges from about 5° C. to about 90° C. and, when the situs comprises a fabric, the water to fabric ratio is typically from about 1:1 to about 30:1.

Packaging Comprising Benefit Agent Delivery Compositions

In one aspect, packaging comprising the benefit agent delivery compositions is disclosed. Such packaging may be used to package a product such as a consumer product. The benefit delivery compositions of the present invention may be adhered or attached any where on such packaging. Such packing may take any form including wrapping, or a container. In one aspect, a benefit agent delivery composition disclosed herein may be adhered or attached to the exterior and/or the interior surface of such packaging. In one aspect, said packaging may comprise a container comprising a cap and said benefit agent delivery composition disclosed herein is adhered or attached to the exterior or interior surface of said cap.

Displays Comprising Benefit Agent Delivery Compositions

In one aspect, a display comprising the benefit agent delivery compositions is disclosed. Such display may be used to attract attention to, market and/or assist in whole or in part the sale of a product such as a consumer product. The benefit delivery compositions of the present invention may be adhered or attached any where on such display. Such display may take any form including posters, sales and/or marketing literature, or a container. In one aspect, a benefit agent delivery composition disclosed herein is adhered or attached to the exterior and/or the interior surface of such display.

EXAMPLES

While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.

Example 1

Equal amounts a perfume composition and amine-terminated Hycar® ATBN1300X42 from Noveon are weighted and mixed for five minutes using a Ultra-Turrax as needed. The ingredients are put at 60° C. in warm water bath for 1 hour before use/mixing. After mixing the mixture is put in a warm water bath at 60° C. for ±12 hours. A homogenous, viscous and sticky material is obtained.

In the same way as described above different ratios between the components can be used:

Weight % Perfume composition 40 50 60 70 80 Hycar ® 1300X42 60 50 40 30 20

Example 2

A mixture comprising 50% of a perfume composition, 40% of carboxyl-terminated Hycar ® 1300X18 (CAS#0068891-50-9) from Noveon, (put at 60° C. in warm water bath for 1 hour before mixing) and 10% of Lupasol® WF(CAS#09002-98-6) from BASF (put at 60° C. in warm water bath for 1 hour before mixing). Mixing is achieved by mixing for five minutes using a Ultra-Turrax T25 Basic equipment (from IKA). After mixing, the mixture is put in a warm water bath at 60° C. for ±12 hours. A homogenous, viscous and sticky material is obtained. In the same way as described above different ratios between the components can be used:

Weight % Perfume composition 40 50 60 70 80 Lupasol ® WF 12 10 8 6 4 Hycar ® 48 40 32 24 16 CTBN1300X18

Weight % Perfume composition 50 50 50 50 50 50 50 50 Lupasol ® WF 2.5 5 7.5 10 12.5 15 17.5 20 Hycar ® CTBN 47.5 45 42.5 40 37.5 35 32.5 30 1300X18

Example 3

A mixture comprising 50% of a perfume composition, 40% of carboxyl-terminated Hycar® CTBN 1300X18 from Noveon (put at 60° C. in warm water bath for 1 hour before mixing) and 10% of Lupasol® WF (CAS#09002-98-6) from BASF (put at 60° C. in warm water bath for 1 hour before use) is formed.

Mixing is achieved by mixing for five minutes using a Ultra-Turrax T25 Basic equipment (from IKA). After mixing, the mixture is put in a warm water bath at 60° C. for ±12 hours. A homogenous, viscous and sticky material is obtained.

Example 4

In a first step of the preparation the Lupasol® WF (CAS#09002-98-6) from BASF 15% is used in combination with 35% of carboxyl-terminated Hycar® CTBN1300X18 and 17% of this polymer mix is diluted with 83% of Benzyl Benzoate to make a workable solution. The materials described above are put together, in the ratio's described above, in a glass jar at 80° C. on a hot plate with stirring using a magnetic stirrer. Next the polymer premix is mixed with a perfume composition in a 1:1 ratio. This polymer—perfume mix is than added to a fabric enhancer composition.

Example 5 Agglomeration of Benefit Agent Delivery Composition—Perfume System for use in Powder Detergents

Starting from any of Examples 1 to 3 as described above:

The resulting homogenous, viscous and sticky material is held at 60° for ±2 hours before starting the agglomeration process. Next, a mixture comprising 40% of the viscous, sticky sample and 60% of melted TAE80 is formed by combining and mixing with an Ultra-Turrax T25 Basic equipment (from IKA) for 5 to 10 minutes. Then, 1 part of the TAE80/sticky sample is very slowly added to 0.6 parts of light soda ash using a Braun kitchen robot to form agglomerates. The resulting agglomerates are then used in a powder detergent.

Example 6 Liquid Application

Starting from any of Examples 1 to 3 as described above:

The resulting homogenous, viscous and sticky material is held at 60° for ±2 hours before starting the dilution process.

Weight % Sticky sample 20 30 40 50 60 Benzyl benzoate or 80 70 60 50 40 fatty acid

The viscous sticky material obtained as described in any of Examples 1-3 above are mixed at different ratios for five minutes using an Ultra-Turrax T25 Basic equipment (from IKA), at the levels listed in the table above, with benzyl benzoate before the resulting mixture is a added to a liquid detergent.

Example 7

Different process manner of obtaining the consumer benefit delivery agent system. Addition of the different ingredients without premixing of the materials: The following are mixed without premixing/premixtures being formed.

Weight % Perfume composition 40 50 60 70 Lupasol ® wf 12 10 8 6 Via premix in H2O (50%/50%) Hycar ® CTBN 1300X18 48 40 32 24 Via premix in Benzyl Benzoate (20%/80% Benzyl Benzoate)

Example 8

Non-limiting examples of product formulations containing a benefit agent delivery composition are summarized in the following table.

EXAMPLES (% wt) XI XII XIII XIV XV XVI XVII XVIII XIX XX FSAa 14 16.47 14 12 12 16.47 — — 5 5 FSAb — 3.00 — — — FSAc — — 6.5 — — Ethanol 2.18 2.57 2.18 1.95 1.95 2.57 — — 0.81 0.81 Isopropyl — — — — — — 0.33  1.22 — — Alcohol Starchd 1.25 1.47 2.00 1.25 — 2.30 0.5  0.70 0.71 0.42 Benefit agent 0.6 0.75 0.6 0.75 0.37 0.60 0.37 0.6 0.37 0.37 delivery composition Phase 0.21 0.25 0.21 0.21 0.14 — —  0.14 — — Stabilizing Polymerf Suds — — — — — — — 0.1 — — Suppressorg Calcium 0.15 0.176 0.15 0.15 0.30 0.176 — 0.1-0.15 — — Chloride DTPAh 0.017 0.017 0.017 0.017 0.007 0.007 0.20 — 0.002 0.002 Preservative 5 5 5 5 5 5 — 250j   5 5 (ppm)i, j Antifoamk 0.015 0.018 0.015 0.015 0.015 0.015 — — 0.015 0.015 Dye 40 40 40 40 40 40 11 30-300 30 30 (ppm) Ammonium 0.100 0.118 0.100 0.100 0.115 0.115 — — — — Chloride HCl 0.012 0.014 0.012 0.012 0.028 0.028 0.016  0.025 0.011 0.011 Structurantl 0.01 0.01 0.01 0.01 0.01 0.01 0.01  0.01 0.01 0.01 Neat 0.8 0.7 0.9 0.5 1.2 0.5 1.1 0.6 1.0 0.9 Perfume Deionized * * * * * * * * * * Water *Balance aN,N-di(tallowoyloxyethyl)-N,N-dimethylammonium chloride. bMethyl bis(tallow amidoethyl)2-hydroxyethyl ammonium methyl sulfate. cReaction product of Fatty acid with Methyldiethanolamine in a molar ratio 1.5:1, quaternized with Methylchloride, resulting in a 1:1 molar mixture of N,N-bis(stearoyl-oxy-ethyl) N,N-dimethyl ammonium chloride and N-(stearoyl-oxy-ethyl) N,-hydroxyethyl N,N dimethyl ammonium chloride. dCationic high amylose maize starch available from National Starch under the trade name CATO ®. fCopolymer of ethylene oxide and terephthalate having the formula described in U.S. Pat. No. 5,574,179 at col.15, lines 1-5, wherein each X is methyl, each n is 40, u is 4, each R1 is essentially 1,4-phenylene moieties, each R2 is essentially ethylene, 1,2-propylene moieties, or mixtures thereof. gSE39 from Wacker hDiethylenetriaminepentaacetic acid. iKATHON ® CG available from Rohm and Haas Co. “PPM” is “parts per million.” jGluteraldehyde kSilicone antifoam agent available from Dow Corning Corp. under the trade name DC2310. lHydrophobically-modified ethoxylated urethane available from Rohm and Haas under the tradename Aculan 44.

Example 9 Benefit Agent Delivery Composition in Dry Laundry Formulations

% w/w granular laundry detergent composition Component A B C D E F G Brightener 0.1 0.1 0.1 0.2 0.1 0.2 0.1 Soap 0.6 0.6 0.6 0.6 0.6 0.6 0.6 Ethylenediamine disuccinic acid 0.1 0.1 0.1 0.1 0.1 0.1 0.1 Acrylate/maleate copolymer 1.5 1.5 1.5 1.5 1.5 1.5 1.5 Hydroxyethane di(methylene 0.4 0.4 0.4 0.4 0.4 0.4 0.4 phosphonic acid) Mono-C12-14 alkyl, di-methyl, 0.5 0.5 0.5 0.5 0.5 0.5 0.5 mono-hydroxyethyl quaternary ammonium chloride Linear alkyl benzene 0.1 0.1 0.2 0.1 0.1 0.2 0.1 Linear alkyl benzene sulphonate 10.3 10.1 19.9 14.7 10.3 17 10.5 Magnesium sulphate 0.4 0.4 0.4 0.4 0.4 0.4 0.4 Sodium carbonate 19.5 19.2 10.1 18.5 29.9 10.1 16.8 Sodium sulphate 29.6 29.8 38.8 15.1 24.4 19.7 19.1 Sodium Chloride 0.1 0.1 0.1 0.1 0.1 0.1 0.1 Zeolite 9.6 9.4 8.1 18 10 13.2 17.3 Photobleach particle 0.1 0.1 0.2 0.1 0.2 0.1 0.2 Blue and red carbonate speckles 1.8 1.8 1.8 1.8 1.8 1.8 1.8 Ethoxylated Alcohol AE7 1 1 1 1 1 1 1 Tetraacetyl ethylene diamine 0.9 0.9 0.9 0.9 0.9 0.9 0.9 agglomerate (92 wt % active) Citric acid 1.4 1.4 1.4 1.4 1.4 1.4 1.4 PDMS/clay agglomerates (9.5% wt % 10.5 10.3 5 15 5.1 7.3 10.2 active PDMS) Polyethylene oxide 0.2 0.2 0.2 0.2 0.2 0.2 0.2 Enzymes e.g. Protease (84 mg/g active), 0.2 0.3 0.2 0.1 0.2 0.1 0.2 Amylase (22 mg/g active) Suds suppressor agglomerate 0.2 0.2 0.2 0.2 0.2 0.2 0.2 (12.4 wt % active) Sodium percarbonate (having 7.2 7.1 4.9 5.4 6.9 19.3 13.1 from 12% to 15% active AvOx) Perfume oil 0.5 0.5 0.5 0.5 0.5 0.5 0.5 Solid perfume particles 0.4 0 0.4 0.4 0.4 0.4 0.6 Benefit agent delivery composition 1.3 2.4 1 1.3 1.3 1.3 0.7 Water 1.4 1.4 1.4 1.4 1.4 1.4 1.4 Misc. 0.1 0.1 0.1 0.1 0.1 0.1 0.1 Total Parts 100 100 100 100 100 100 100

Example 10 Liquid Laundry Formulations (HDLs)

Ingredient HDL 1 HDL 2 HDL3 HDL4 HDL 5 HDL 6 Alkyl Ether Sulphate 0.00 0.50 12.0 12.0 6.0 7.0 Dodecyl Benzene 8.0 8.0 1.0 1.0 2.0 3.0 Sulphonic Acid Ethoxylated Alcohol 8.0 6.0 5.0 7.0 5.0 3.0 Citric Acid 5.0 3.0 3.0 5.0 2.0 3.0 Fatty Acid 3.0 5.0 5.0 3.0 6.0 5.0 Ethoxysulfated 1.9 1.2 1.5 2.0 1.0 1.0 hexamethylene diamine quaternized Diethylene triamine penta 0.3 0.2 0.2 0.3 0.1 0.2 methylene phosphonic acid Enzymes 1.20 0.80 0 1.2 0 0.8 Brightener (disulphonated 0.14 0.09 0 0.14 0.01 0.09 diamino stilbene based FWA) Cationic hydroxyethyl cellulose 0 0 0.10 0 0.200 0.30 Poly(acrylamide-co- 0 0 0 0.50 0.10 0 diallyldimethylammonium chloride) Hydrogenated Castor Oil 0.50 0.44 0.2 0.2 0.3 0.3 Structurant Boric acid 2.4 1.5 1.0 2.4 1.0 1.5 Ethanol 0.50 1.0 2.0 2.0 1.0 1.0 1,2 propanediol 2.0 3.0 1.0 1.0 0.01 0.01 Glutaraldehyde 0 0 19 ppm 0 13 ppm 0 Diethyleneglycol (DEG) 1.6 0 0 0 0 0 2,3-Methyl-1,3- 1.0 1.0 0 0 0 0 propanediol (M pdiol) Mono Ethanol Amine 1.0 0.5 0 0 0 0 NaOH Sufficient To pH 8 pH 8 pH 8 pH 8 pH 8 pH 8 Provide Formulation pH of: Sodium Cumene 2.00 0 0 0 0 0 Sulphonate (NaCS) Silicone (PDMS) emulsion 0.003 0.003 0.003 0.003 0.003 0.003 Perfume 0.7 0.5 0.8 0.8 0.6 0.6 Polyethyleneimine 0.01 0.10 0.00 0.10 0.20 0.05 Benefit Agent Delivery 1.00 5.00 1.00 2.00 0.10 0.80 Composition Water Balance Balance Balance Balance Balance Balance to to to to to to 100% 100% 100% 100% 100% 100%

The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and functionally equivalent range surrounding that value. For example, a dimension disclosed as “40 mm” is intended to mean “about 40 mm”.

All documents cited in the Detailed Description of the Invention are, in relevant part, incorporated herein by reference; the citation of any document is not to be construed as an admission that it is prior art with respect to the present invention. To the extent that any meaning or definition of a term in this document conflicts with any meaning or definition of the same term in a document incorporated by reference, the meaning or definition assigned to that term in this document shall govern.

While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.

Claims

1. A consumer product composition comprising:

a.) from about 0.001% to about 10% of a consumer benefit agent delivery composition comprising: (i) from about 5% to about 95% by weight of a benefit agent; (ii) from about 5% to about 70% by weight of a polymeric compound; (iii) from about 0% to about 50% by weight of a cross-linking agent; and
b.) a consumer product ingredient.

2. A consumer product composition according to claim 1 comprising:

a.) from about 0.001% to about 10% of a consumer benefit agent delivery composition comprising: (i) from about 30% to about 85% by weight of a benefit agent; (ii) from about 20% to about 60% by weight of a polymeric compound; (iii) from about 0% to about 10% by weight of a cross-linking agent; and
b.) a consumer product ingredient.

3. A consumer product composition according to claim 2 comprising:

a.) from about 0.001% to about 10% of a consumer benefit agent delivery composition comprising: (i) from about 40% to about 60% by weight of a benefit agent; (ii) from about 30% to about 55% by weight of a polymeric compound; (iii) from about 1% to about 7% by weight of a cross-linking agent; and
b.) a consumer product ingredient.

4. The composition of claim 1, wherein said benefit agent is selected from the group consisting of a perfume raw material, a fragrance, a perfume, an essential oil, an insecticide, an insect repellant, a pesticide, a herbicide, an odorant, a malodor counteractant, an odor masking agent, a cooling agent, a vitamin, softening agent, a skin care agent, a silicone, a softening agent, an encapsulated perfume and combinations thereof.

5. The composition of claim 2, wherein said benefit agent is selected from the group consisting of a fragrance, a perfume, an essential oil, an insecticide, an insect repellant, a pesticide, a herbicide, an odorant, a malodor counteractant, an odor masking agent, a cooling agent, a vitamin, softening agent, a skin care agent, a silicone, a softening agent, an encapsulated perfume and combinations thereof.

6. The composition of claim 3, wherein said benefit agent is selected from the group consisting of a fragrance, a perfume, an essential oil, an insecticide, an insect repellant, a pesticide, a herbicide, an odorant, a malodor counteractant, an odor masking agent, a cooling agent, a vitamin, softening agent, a skin care agent, a silicone, a softening agent, an encapsulated perfume and combinations thereof.

7. The composition of claim 1, wherein said polymeric compound comprises polybutadiene, polybutadiene-styrene, polyisoprene, polybutadiene-acrylonitrile or mixtures thereof.

8. The composition of claim 2, wherein said polymeric compound comprises polybutadiene, polybutadiene-styrene, polyisoprene, polybutadiene-acrylonitrile or mixtures thereof.

9. The composition of claim 3, wherein said polymeric compound comprises polybutadiene, polybutadiene-styrene, polyisoprene, polybutadiene-acrylonitrile or mixtures thereof.

10. The composition of claim 1, wherein said polymeric compound comprises, per polymeric compound, at least two moieties selected from the moieties consisting of a carboxylic acid moiety, an amine moiety, a hydroxyl moiety, and a nitrile moiety.

11. The composition of claim 2, wherein said polymeric compound comprises, per polymeric compound, at least two moieties selected from the moieties consisting of a carboxylic acid moiety, an amine moiety, a hydroxyl moiety, and a nitrile moiety.

12. The composition of claim 3, wherein said polymeric compound comprises, per polymeric compound, at least two moieties selected from the moieties consisting of a carboxylic acid moiety, an amine moiety, a hydroxyl moiety, and a nitrile moiety.

13. The composition of claim 1, wherein said cross-linking agent comprises a polyamine.

14. The composition of claim 13 wherein said polyamine comprises diethylenetriamine, ethylene diamine, polyethyleneimine, polyvinylamine, bis(3-aminopropyl)piperazine, N,N-Bis-(3-aminopropyl)methylamine, tris(2-aminoethyl)amine or mixtures thereof.

15. A method for making a benefit agent delivery composition comprising:

a.) mixing a first mixture, wherein said first mixture comprises: from about 15% to about 95% by weight of a volatile hydrophobic liquid; and from about 3% to about 40% by weight of a polymeric compound containing a carboxylic acid, until said first mixture is completely mixed; and mixing into said first mixture, from about 1.5% to about 40% by weight of a cross-linking agent; or
b.) mixing a first mixture, wherein said first mixture comprises: from about 15% to about 95% by weight of a volatile hydrophobic liquid; and from about 3% to about 40% by weight of a polymeric compound containing a carboxylic acid, until said first mixture is completely mixed; and mixing into said first mixture, from about 0% to about 40% by weight of a cross-linking agent; or
c.) mixing a first mixture, wherein said first mixture comprises: from about 15% to about 95% by weight of a volatile hydrophobic liquid; and from about 3% to about 40% by weight of a polymeric compound containing a carboxylic acid, until said first mixture is completely mixed; and mixing into said first mixture a second mixture, wherein said second mixture comprises: from 15% to about 95% by weight volatile hydrophobic liquid; and from about 1.5% to about 40% by weight of a cross-linking agent; or
d.) combining from about 15% to about 95% by weight of a volatile hydrophobic liquid; and from about 3% to about 40% by weight of a polymeric compound containing a carboxylic acid, until said first mixture is completely mixed; and mixing into said first mixture, from about 0% to about 40% by weight of a cross-linking agent;
e.) optionally combining the mixtures produced in a.), b.), c.) and/or d.) with a diluent and/or a surfactant; and/or further processing the mixtures produced in a.), b.), c.) and/or d.) to form a particle, bead and/or agglomerate.

16. The method of claim 15, wherein the hydrophobic liquid is selected from the group consisting of fragrance, perfume, perfume microcapsules, essential oil, insecticide, insect repellant, pesticide, herbicide, odorant, malodor counteractant, odor masking agent and mixtures thereof.

17. The method of claims 15, wherein the polymeric compound comprises polybutadiene, polybutadiene-styrene, polyisoprene, polybutadiene-acrylonitrile or mixtures thereof.

18. The method of claim 17, wherein said polymeric compound contains at least 2.0 carboxylic acid, amine or hydroxyl groups per groups per polymeric compound.

19. A consumer product comprising a composition according to any of claim 1 and packaging, said composition being attached or adhered to said packaging.

20. A display comprising a composition according to any of claim 1 and a display material, said composition being attached or adhered to said display material.

21. A cleaning and/or treatment composition or fabric care composition comprising a composition according to any one of claim 1 and at least one cleaning and/or treatment composition or fabric care adjunct ingredient.

22. A method of treating and/or cleaning a situs, said method comprising

a.) optionally washing and/or rinsing said situs;
b.) contacting said situs with a composition according to any one of claim 1 and/or 21; and
c.) optionally washing and/or rinsing said situs.

23. A situs treated with a composition according to any one of claim 1 and/or 21.

Patent History
Publication number: 20080200359
Type: Application
Filed: Feb 15, 2008
Publication Date: Aug 21, 2008
Inventors: Johan Smets (Lubbeek), Pascale Claire Annick Van Steenwinckel (Weerde)
Application Number: 12/070,093