US20080200359A1 - Benefit agent delivery compositions - Google Patents

Benefit agent delivery compositions Download PDF

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Publication number
US20080200359A1
US20080200359A1 US12/070,093 US7009308A US2008200359A1 US 20080200359 A1 US20080200359 A1 US 20080200359A1 US 7009308 A US7009308 A US 7009308A US 2008200359 A1 US2008200359 A1 US 2008200359A1
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composition
weight
agent
polymeric compound
mixture
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US12/070,093
Inventor
Johan Smets
Pascale Claire Annick Van Steenwinckel
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Procter and Gamble Co
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Procter and Gamble Co
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Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to US12/070,093 priority patent/US20080200359A1/en
Assigned to PROCTER & GAMBLE COMPANY, THE reassignment PROCTER & GAMBLE COMPANY, THE ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SMETS, JOHAN, VAN STEENWINCKEL, PASCALE CLAIRE ANNICK
Publication of US20080200359A1 publication Critical patent/US20080200359A1/en
Application status is Abandoned legal-status Critical

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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/50Perfumes
    • C11D3/502Protected perfumes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION, OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS, OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS, OR SURGICAL ARTICLES
    • A61L9/00Disinfection, sterilisation or deodorisation of air
    • A61L9/01Deodorant compositions

Abstract

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.

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 (23)

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.
US12/070,093 2007-02-15 2008-02-15 Benefit agent delivery compositions Abandoned US20080200359A1 (en)

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CA2675426A1 (en) 2008-08-21
WO2008100625A1 (en) 2008-08-21

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