WO2011084463A1 - Freshening compositions comprising malodor binding polymers and malodor control components - Google Patents

Freshening compositions comprising malodor binding polymers and malodor control components Download PDF

Info

Publication number
WO2011084463A1
WO2011084463A1 PCT/US2010/060466 US2010060466W WO2011084463A1 WO 2011084463 A1 WO2011084463 A1 WO 2011084463A1 US 2010060466 W US2010060466 W US 2010060466W WO 2011084463 A1 WO2011084463 A1 WO 2011084463A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition
malodor
aldehyde
methyl
perfume
Prior art date
Application number
PCT/US2010/060466
Other languages
French (fr)
Inventor
Ricky Ah-Man Woo
Christine Marie Readnour
Jason John Olchovy
Michael-Vincent Nario Malanyaon
Zaiyou Liu
Rhonda Jean Jackson
Kristin Rhedrick Williams
Carla Jean Colina
Cahit Eylem
Lon Montgomery Gray
Shih-Chuan Liou
Steven Anthony Horenziak
Original Assignee
The Procter & Gamble Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to US61/287,348 priority Critical
Priority to US28734809P priority
Priority to US28736909P priority
Priority to US28738309P priority
Priority to US61/287,383 priority
Priority to US61/287,369 priority
Priority to US12/885,884 priority
Priority to US12/885,884 priority patent/US20110150817A1/en
Priority to US12/904,261 priority
Priority to US12/904,261 priority patent/US20110305659A1/en
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Publication of WO2011084463A1 publication Critical patent/WO2011084463A1/en

Links

Classifications

    • 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
    • A61L9/014Deodorant compositions containing sorbent material, e.g. activated carbon
    • 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
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0068Deodorant compositions
    • 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
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2072Aldehydes-ketones
    • 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
    • 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
    • A61L2209/00Aspects relating to disinfection, sterilisation or deodorisation of air
    • A61L2209/20Method-related aspects
    • A61L2209/21Use of chemical compounds for treating air or the like

Abstract

Freshening compositions comprising a malodor binding polymer, malodor control components, and an aqueous carrier; and methods thereof are provided. In some embodiments, the freshening composition comprises a homopolymeric polyethylenimine having a molecular weight of about 1,000 to about 2,000,000 and a mixture of volatile aldehydes. Such freshening compositions may be used to reduce malodor and/or microbes on inanimate surfaces or in the air.

Description

FRESHENING COMPOSITIONS COMPRISING MALODOR BINDING POLYMERS AND

MALODOR CONTROL COMPONENTS

FIELD OF THE INVENTION

The present invention relates to freshening compositions comprising a malodor binding polymer, malodor control components, and an aqueous carrier; and methods thereof.

BACKGROUND OF THE INVENTION

Freshening products for reducing or masking malodors on fabrics and in air are currently available and are described in the patent literature. The Procter & Gamble Company sells fabric and air freshening products under the FEBREZE® brand name. These products typically contain perfume, solubilizer, cyclodextrin, and an aqueous carrier. S. C. Johnson sells products such as Glade® Fabric and Air Odor Eliminator and Oust® Surface Disinfectant and Air Sanitizer. Reckitt-Benckiser sells products such as Lysol® Disinfectant Spray.

Certain freshening compositions do not effectively neutralize a broad range of malodors on fabrics and in the air. Further, the time required for a composition to noticeably combat malodors may create consumer doubt as to a product's efficacy on malodors. For example, the consumer may leave the treated space before the product begins to noticeably reduce the malodor.

There remains a need for improved freshening compositions that neutralize a broad range of malodors, including amine-base and sulfur-based malodors and malodors caused by microbes, while not overpowering malodors with overwhelming perfume.

SUMMARY OF THE INVENTION

The present invention relates to a freshening composition for reducing malodor. According to one embodiment, there is provided a freshening composition for reducing malodor comprising: an effective amount of a malodor binding polymer; a malodor control component comprising an effective amount of a mixture of two or more volatile aldehydes for neutralizing a malodor, wherein said two or more volatile aldehydes are selected from the group consisting of 2-ethoxy benzylaldehyde, 2-isopropyl-5-methyl-2-hexenal, 5-methyl furfural, 5-methyl- thiophene-carboxaldehyde, adoxal, p-anisaldehyde, benzylaldehyde, bourgenal, cinnamic aldehyde, cymal, decyl aldehyde, floral super, florhydral, helional, lauric aldehyde, ligustral, lyral, melonal, o-anisaldehyde, pino acetaldehyde, P.T. bucinal, thiophene carboxaldehyde, trans- 4-decenal, trans trans 2,4-nonadienal, undecyl aldehyde, and mixtures thereof; and an aqueous carrier.

In another embodiment, there is provided a freshening composition for reducing malodor comprising: an effective amount of a malodor binding polymer; and a malodor control component comprising at least one volatile aldehyde and an acid catalyst having a vapor pressure of about 0.01 to about 13 at 25°C.

The present invention also relates to methods of reducing malodor comprising the steps of: providing a freshening composition comprising an effective amount of a malodor binding polymer and a malodor control component; and dispersing an effective amount of said freshening composition on an inanimate surface or in the air.

BRIEF DESCRIPTION OF THE DRAWINGS

Fig. 1 is a bar graph showing the reduction of aldehydic malodors evaporating off fabrics treated with freshening compositions according to the present invention containing a malodor binding polymer in comparison to a freshening composition lacking such malodor binding polymer.

Fig. 2 is a bar graph showing microbe reduction with a freshening composition according to the present invention containing a malodor binding polymer in comparison to a freshening composition lacking such malodor binding polymer.

Fig. 3 is a graph showing the performance of one embodiment of a malodor control component, in accordance with the present invention, on a sulfur-based malodor.

Fig. 4 is a graph showing the performance of one embodiment of a malodor control component, in accordance with the present invention, on an amine-based malodor.

Fig. 5 is a graph showing butanethiol reduction by thiophene carboxaldehyde in combination with various acid catalysts.

DETAILED DESCRIPTION OF THE INVENTION

The freshening composition of the present invention is designed to deliver genuine malodor reduction and not function merely by using perfume to cover up or mask odors. The freshening composition reduces malodor in the air or on inanimate surfaces, for example, fabrics that are contaminated with environmental odors such as food and tobacco odors, or wetted with perspiration. The freshening composition may also reduce microbes on inanimate surfaces or in air. The freshening composition may also act as a barrier to prevent malodors from adhering to or penetrating an inanimate surface.

A genuine malodor reduction provides a sensory and analytically measurable (e.g. gas chromatograph) malodor reduction. Thus, if the freshening composition delivers a genuine malodor reduction, the freshening composition will neutralize malodors in the air and/or on fabrics. "Neutralize" or "neutralization" as used herein means chemically reacting with malodor components (e.g. the reaction of primary amines with aldehydes to form imines, reductive alkylation of amines, protonation and deprotonation of amines, polymerization or de- polymerization); or suppressing the volatility of malodorous components such that other parts of the composition may react (e.g. acid - base neutralization); or physically entrapping odorous molecules such that they are not re-released into the air (e.g. cyclodextrin inclusion complexes as described herein). Odor neutralization may be distinguished from odor masking or odor blocking by a change in the malodorous compound, as opposed to a change in the ability to perceive the malodor without any corresponding change in the condition of the malodorous compound.

I. Freshening Composition

The freshening composition for reducing malodor comprises a malodor binding polymer, a malodor counteractant comprising at least one aliphatic aldehyde, and an aqueous carrier, wherein said composition is essentially free of materials that soil or stain fabric. The total amount of surfactants (e.g. solubilizer, wetting agent) in the freshening composition is from 0% to 3% or no more than 3%, alternatively from 0% to 1% or no more than 1%, alternatively from 0% to 0.9% or no more than 0.9%, alternatively from 0% to 0.7 or no more than 0.7%, alternatively from 0% to 0.5% or no more than 0.5%, alternatively from 0% to 0.3% or no more than 0.3%, by weight of the composition. Compositions with higher concentrations can make fabrics susceptible to soiling and/or leave unacceptable visible stains on fabrics as the solution evaporates. A. Malodor Binding Polymer

The freshening composition of the present invention includes a malodor binding polymer. A malodor binding polymer is polymer having an available functional group (e.g. at least one primary amine) that has the affinity to neutralize malodor components. Monomers having an available function group with an affinity to neutralize malodor components are also contemplated.

A malodor binding polymer may include amine based compounds, such as monoamines, amino acids, polyethyleneimine polymers (PEIs), modified PEIs, substituted PEIs; acrylic acid polymers, such as polyacrylate co-polymer (e.g. Acumer™ 9000 from Rohm & Haas), polyacrylic acid polymers (e.g. Acusol™ from Rohm & Haas), and modified acrylate copolymers (e.g. Aculyn™ from Rohm & Haas); and modified methacrylate copolymers (e.g. HydroSal™ from Salvona Technologies); or mixtures thereof.

1. Amine based compounds

In some embodiments, the malodor binding polymer is an amine based compound with a molecular weight greater than 100 Daltons and at least 10% of its amine groups are primary amines. In one embodiment, the amine-based compound will be a polyamine with a molecular weight greater than 150 Daltons and 15% to 80% of its amine groups are primary amines. In another embodiment, the malodor binding polymer is an amine-based compound with a molecular weight greater than 1000 Daltons and from 0% to about 10% or less than 10% of its amine groups are primary amines.

A general structure for a primary amine compound useful in this invention is as follows:

B-(NH2)n;

wherein B is a carrier material, and n is an index of value of at least 1. Suitable B carriers include both inorganic and organic carrier moieties. By "inorganic carrier", it is meant a carrier which is comprised of non- or substantially non-carbon based backbones.

Compounds containing a secondary amine group have a structure similar to the above with the exception that the compound comprises one or more -NH- groups as well as -N¾ groups. The amine compounds of this general type may be relatively viscous materials.

Exemplary amine based compounds are those selected from monoamines, aminoaryl derivatives, poly amines and derivatives thereof, poly amino acids and copolymers thereof, glucamines, dendrimers, PEIs, substituted amines and amides monoamines, or mixtures thereof, a. Monoamines

Monoamines may be utilized in the present invention. Nonlimiting examples of suitable monoamines for use in the present invention include, but are not limited to, primary amines that also contain hydroxy and/or alkoxy functional groups, such as the 2-hydroxyamines and/or 3- hydroxy amines; primary or secondary amines that also contain a functional group that enhances deposition of the monoamine compared to monoamines that lack that functional group, especially when the monoamine is interacting with the benefit agent. Primary monoamines may also be used herein in combination with secondary monoamines. However, sufficient levels of the primary monoamine must be used to provide at least 10% of the total amine groups within such combinations as primary amine groups.

b. Aminoaryl derivatives

Exemplary aminoaryl derivatives are the amino-benzene derivatives including the alkyl esters of 4-amino benzoate compounds, ethyl-4-amino benzoate, phenylethyl-4-aminobenzoate, phenyl-4-aminobenzoate, 4-amino-N'-(3-aminopropyl)-benzarnide, or mixtures thereof.

c. Polyamines

Examples of suitable amino functional polymers containing at least one primary amine group for the purposes of the present invention are:

- Polyvinylamine with a MW of 300-2.10E6 Daltons (e.g Lupamine series 1500, 4500, 5000, 9000 available from BASF);

- Polyvinylamine alkoxylated with a MW of > 600 Daltons and a degree of ethoxylation of at least 0.5;

- Polyvinylamine vinylalcohol - molar ratio 2:1, polyvinylaminevinylformamide - molar ratio 1:2 and polyvinylamine vinylformamide-molar ratio 2:1;

- Triethylenetetramine, diethylenetriamine, tetraethylenepentamine;

- Bis-aminopropylpiperazine;

- amino substituted polyvinylalcohol with a MW ranging from 400-300,000 Daltons;

- polyoxyethylene bis [amine] available from e.g. Sigma;

- polyoxyethylene bis [6-aminohexyl] available from e.g. Sigma;

- N,N'-bis-(3-aminopropyl)-l,3-propanediamine linear or branched (TPTA);

- N,N'-bis-(3-arninopropyl)ethylenediarnine;

- bis (amino alkyl) alkyl diamine, linear or branched; and

- l,4-bis-(3-aminopropyl) piperazine (BNPP).

d. Polyamino Acids

Suitable amine based compounds include polyamino acids. Polyamino acids are made up of amino acids or chemically modified amino acids. The amino acids may be selected from cysteine, histidine, isoleucine, tyrosine, tryptophane, leucine, lysine, glutamic acid, glutamine, glycine, alanine, aspartic acid, arginine, asparagine, phenylalanine, proline, serine, histidine, threonine, methionine, valine, and mixtures thereof. Amino acid derivatives may be tyrosine ethylate, glycine methylate, tryptophane ethylate, or mixtures thereof; homopolymers of amino acids; hydroxy amines; polyamino acids; or mixtures thereof.

In chemically modified amino acids, the amine or acidic function of the amino acid has reacted with a chemical reagent. This is often done to protect these chemical amine and acid functions of the amino acid in a subsequent reaction or to give special properties to the amino acids, like improved solubility. Examples of such chemical modifications are benzyloxycarbonyl, aminobutyric acid, butyl ester, and pyroglutamic acid. More examples of common modifications of amino acids and small amino acid fragments can be found in the Bachem, 1996, Peptides and Biochemicals Catalog.

One polyamino acid is polylysine, alternatively poly lysines or polyamino acids where more than 50% of the amino acids are lysine, since the primary amine function in the side chain of the lysine is the most reactive amine of all amino acids. One polyamino acid has a molecular weight of 500 to 10,000,000, alternatively between 2000 and 25,000.

The polyamino acid can be cross linked. The cross linking can be obtained for example by condensation of the amine group in the side chain of the amino acid like lysine with the carboxyl function on the amino acid or with protein cross linkers like PEG derivatives. The cross linked polyamino acids still need to have free primary and/or secondary amino groups left for neutralization. Cross linked polyamino acid has a molecular weight of 20,000 to 10,000,000; alternatively between 200,000 and 2,000,000.

The polyamino acid or the amino acid can be co-polymerized with other reagents like for instance with acids, amides, acyl chlorides, aminocaproic acid, adipic acid, ethylhexanoic acid, caprolactam, or mixtures thereof. The molar ratio used in these copolymers ranges from 1:1 (reagent/ amino acid (lysine)) to 1:20, alternatively from 1:1 to 1:10. The polyamino acid like polylysine can be unethoxylated or partially ethoxylated so long as the requisite amount of primary amine remains in the polymer.

e. Dendrimers

Also useful amine based compounds are polypropylenimine dendrimers and the commercially available Starburst® polyamidoamines (PAMAM) dendrimers, generation G0-G10 from Dendritech and the dendrimers Astromols®, generation 1-5 from DSM being DiAminoButane Poly Amine DAB (PA)x dendrimers with x = 2nx4 and n being generally comprised between 0 and 4.

f. PEIs In one embodiment, the malodor binding polymer is a PEL It has been surprisingly discovered that amine based polymers at a pH of about 4 to about 8, alternatively above 5 to about 8, alternatively 7 can neutralize amine based odors. PEIs have the following general formula:

- ( CH2 - CH2 - NH )n - ; n = 10 - 105

Homopolymeric PEIs are branched, spherical polyamines with a well defined ratio of primary, secondary and tertiary amine functions. They are best described in the following partial structural formula:

Figure imgf000009_0001

The chemical structure of homopolymeric PEIs follows a simple principle: one amine function - two carbons.

The freshening composition may comprise a homopolymeric polyethylenimine having a molecular weight of about 800 to about 2,000,000, alternatively about 1,000 to about 2,000,000, alternatively about 1,200 to about 25,000, alternatively about 1,300 to about 25,000, alternatively about 2,000 to about 25,000, alternatively about 10,000 to about 2,000,000, alternatively about 25,000 to about 2,000,000, alternatively about 25,000. Exemplary homopolymeric PEIs include those that are commercially available under the tradename Lupasol® from BASF. Lupasol products are usually obtained through polymerization of the ethylenimine monomer. The ethylenimine monomer has totally reacted in the polymer matrix. Suitable Lupasol products include Lupasol FG (MW 800), G20wfv (MW 1300), PR8515 (MW 2000), WF (MW 25,000), FC (MW 800), G20 (MW 1300), G35 (MW 1200), GlOO (MW 2000), HF (MW 25,000), P (MW 750,000), PS (MW 750,000), SK (MW 2,000,000), SNA (MW 1,000,000).

In some embodiments, the freshening composition comprises Lupasol HF or WF (MW

25,000), P (MW 750,000), PS (MW 750,000), SK (MW 2,000,000), 620wfv (MW 1300) or PR 1815 (MW 2000), or Epomin SP-103, Epomin SP-110, Epomin SP-003, Epomin SP-006, Epomin SP-012, Epomin SP-018, Epomin SP-200, or partially alkoxylated polyethyleneimine, like polyethyleneirnine 80% ethoxylated from Aldrich. In one embodiment, the freshening composition contains Lupasol WF (MW 25,000).

Also suitable amine based compounds for use in the freshening composition are modified PEIs, partially alkylated polyethylene polymers, PEIs with hydroxyl groups, 1,5-pentanediamine, 1,6-hexanediamine, 1,3 pentanediamine, 3-dimethylpropanediamine, 1,2-cyclohexanediamine, l,3-bis(aminomethyl)cyclohexane, tripropylenetetraamine, bis (3-aminopropyl)piperazine, dipropylenetriamine, tris(2-arninoethylamine), tetraethylenepentamine, bishexamethylenetriamine, bis(3-aminopropyl) 1,6 - hexamethylenediamine, 3,3'-diamino-N- methyldipropylamine, 2-methyl- 1 ,5 -pentanediamine, Ν,Ν,Ν' ,Ν' -tetra(2- aminoethyl)ethylenediamine, N,N,N',N'-tetra(3-aminopropyl)-l,4-butanediamine, pentaethylhexamine, l,3-diamino-2-propyl-tert-butylether, isophorondiamine, 4,4',- diaminodicyclohylmethane, N-methyl-N-(3-aminopropyl)ethanolamine, spermine, spermidine, 1- piperazineethaneamine, 2-(bis(2-aminoethyl)amino)ethanol, ethoxylated N-

(tallowalkyl)trimethylene diamines,poly[oxy(methyl-l,2-ethanediyl)], a-(2-aminomethyl- ethoxy)- (= C.A.S No. 9046-10-0); poly[oxy(methyl-l,2-ethanediyl)], a-hydro-)-co-(2- aminomethylethoxy)-, ether with 2-ethyl-2-(hydroxymethyl)-l,3-propanediol (= C.A.S. No. 39423-51-3); commercially available under the tradename Jeffamines T-403, D-230, D-400, D- 2000; 2,2\2"-triarninotriethylarnine; 2,2'-diamino-diethylamine; 3,3'-diamino-dipropylamine, 1,3 bis aminoethyl-cyclohexane commercially available from Mitsubishi, and the C12 Sternamines commercially available from Clariant like the C12 Sternamin(propylenamine)n with n=3/4.

In one embodiment, the malodor binding polymer may be used in an effective amount to provide a reduction of microbes on fabric and/or in the air. When using a malodor binding polymer, an effective amount reduces microbes by at least 1 log difference as compared to a composition lacking the malodor binding polymer. This difference is then attributed to the use of the malodor binding polymer and not the inherent variability in the microbial species.

Suitable levels of malodor binding polymer are from about 0.01% to about 2%, alternatively from about 0.01% to about 1%, alternatively about 0.01% to about 0.8%, alternatively about 0.01% to about 0.6%, alternatively about 0.01% to about 0.1%, alternatively about 0.01% to about 0.07%, alternatively about 0.07%, by weight of the freshening composition. Compositions with higher amount of malodor binding polymer may make fabrics susceptible to soiling and/or leave unacceptable visible stains on fabrics as the solution evaporates off of the fabric. B. Malodor Control Components

The freshening composition may include malodor control components. The malodor control components are designed to deliver genuine malodor neutralization and not function merely by covering up or masking odors. A genuine malodor neutralization provides a sensory and analytically measurable (e.g. gas chromatograph) malodor reduction. Thus, if the malodor control component delivers a genuine malodor neutralization, the composition will reduce malodors in the vapor and/or liquid phase. When used in combination with the malodor binding polymer, the composition may neutralize a broader range of malodor causing materials which, in turn, further reduces malodors in the air or on inanimate surfaces.

1. Perfume Materials

The malodor control component includes perfume materials which may include a mixture of volatile aldehydes. Volatile aldehyes neutralize malodors in vapor and/or liquid phase via chemical reactions. Aldehydes that are partially volatile may be considered a volatile aldehyde as used herein. Volatile aldehydes may react with amine-based odors, following the path of Schiff-base formation. Volatiles aldehydes may also react with sulfur-based odors, forming thiol acetals, hemi thiolacetals, and thiol esters in vapor and/or liquid phase. It may be desirable for these vapor and/or liquid phase volatile aldehydes to have virtually no negative impact on the desired perfume character of a product.

Suitable volatile aldehydes may have a vapor pressure (VP) in the range of about 0.0001 torr to 100 torr, alternatively about 0.0001 torr to about 10 torr, alternatively about 0.001 torr to about 50 torr, alternatively about 0.001 torr to about 20 torr, alternatively about 0.001 torr to about 0.100 torr, alternatively about 0.001 torr to 0.06 torr, alternatively about 0.001 torr to 0.03 torr, alternatively about 0.005 torr to about 20 torr, alternatively about 0.01 torr to about 20 torr, alternatively about 0.01 torr to about 15 torr, alternatively about 0.01 torr to about 10 torr, alternatively about 0.05 torr to about 10 torr, measured at 25 °C.

The volatile aldehydes may also have a certain boiling point (B.P.) and octanol/water partition coefficient (P). The boiling point referred to herein is measured under normal standard pressure of 760 mmHg. The boiling points of many volatile aldehydes, at standard 760 mm Hg are given in, for example, "Perfume and Flavor Chemicals (Aroma Chemicals)," written and published by Steffen Arctander, 1969.

The octanol/water partition coefficient of a volatile aldehyde is the ratio between its equilibrium concentrations in octanol and in water. The partition coefficients of the volatile aldehydes used in the malodor control component may be more conveniently given in the form of their logarithm to the base 10, logP. The logP values of many volatile aldehydes have been reported. See, e.g., the Pomona92 database, available from Daylight Chemical Information Systems, Inc. (Daylight CIS), Irvine, California. However, the logP values are most conveniently calculated by the "CLOGP" program, also available from Daylight CIS. This program also lists experimental logP values when they are available in the Pomona92 database. The "calculated logP" (ClogP) is determined by the fragment approach of Hansch and Leo (cf., A. Leo, in Comprehensive Medicinal Chemistry, Vol. 4, C. Hansch, P. G. Sammens, J. B. Taylor and C. A. Ramsden, Eds., p. 295, Pergamon Press, 1990). The fragment approach is based on the chemical structure of each volatile aldehyde, and takes into account the numbers and types of atoms, the atom connectivity, and chemical bonding. The ClogP values, which are the most reliable and widely used estimates for this physicochemical property, are preferably used instead of the experimental logP values in the selection of volatile aldehydes for the malodor control component.

The ClogP values may be defined by four groups and the volatile aldehydes may be selected from one or more of these groups. The first group comprises volatile aldehydes that have a B.P. of about 250 °C or less and ClogP of about 3 or less. The second group comprises volatile aldehydes that have a B.P. of 250°C or less and ClogP of 3.0 or more. The third group comprises volatile aldehydes that have a B.P. of 250°C or more and ClogP of 3.0 or less. The fourth group comprises volatile aldehydes that have a B.P. of 250°C or more and ClogP of 3.0 or more. The malodor control component may comprise any combination of volatile aldehydes from one or more of the ClogP groups.

In some embodiments, the malodor control component of the present invention may comprise, by total weight of the malodor control component, from about 0% to about 30% of volatile aldehydes from group 1, alternatively about 25%; and/or about 0% to about 10% of volatile aldehydes from group 2, alternatively about 10%; and/or from about 10% to about 30% of volatile aldehydes from group 3, alternatively about 30%; and/or from about 35% to about 60% of volatile aldehydes from group 4, alternatively about 35%.

Exemplary volatile aldehydes which may be used in a malodor control component include, but are not limited to, Adoxal (2,6,10-Trimethyl-9-undecenal), Bourgeonal (4-t- butylbenzenepropionaldehyde), Lilestralis 33 (2-methyl-4-t-butylphenyl)propanal), Cinnamic aldehyde, cinnamaldehyde (phenyl propenal, 3-phenyl-2-propenal), Citral, Geranial, Neral (dimethyloctadienal, 3,7-dimethyl-2,6-octadien-l-al), Cyclal C (2,4-dimethyl-3-cyclohexen-l- carbaldehyde), Florhydral (3-(3-Isopropyl-phenyl)-butyraldehyde), Citronellal (3,7-dimethyl 6- octenal), Cymal, cyclamen aldehyde, Cyclosal, Lime aldehyde (Alpha- methyl-p-isopropyl phenyl propyl aldehyde), Methyl Nonyl Acetaldehyde, aldehyde C12 MNA (2-methyl-l-undecanal), Hydroxycitronellal, citronellal hydrate (7-hydroxy-3,7-dimethyl octan-l-al), Helional (alpha- methyl-3,4-(methylenedioxy)-hydrocinnamaldehyde, hydrocinnamaldehyde (3-phenylpropanal, 3-phenylpropionaldehyde), Intreleven aldehyde (undec-10-en-l-al), Ligustral, Trivertal (2,4- dimethyl-3-cyclohexene-l-carboxaldehyde), Jasmorange, satinaldehyde (2-methyl-3- tolylproionaldehyde, 4-dimethylbenzenepropanal), Lyral (4-(4-hydroxy-4-methyl pentyl)-3- cyclohexene-l-carboxaldehyde), Melonal (2,6-Dimethyl-5-Heptenal), Methoxy Melonal (6- methoxy-2,6-dimethylheptanal), methoxycinnamaldehyde (trans-4-methoxycinnamaldehyde), Myrac aldehyde isohexenyl cyclohexenyl-carboxaldehyde, trifernal ((3-methyl-4-phenyl propanal, 3-phenyl butanal), lilial, P.T. Bucinal, lysmeral, benzenepropanal (4-tert-butyl-alpha- methyl-hydrocinnamaldehyde), Dupical, tricyclodecylidenebutanal (4-Tricyclo5210- 2,6decylidene-8butanal), Melafleur (1,2,3,4,5, 6,7, 8-octahydro-8,8-dimethyl-2-naphthaldehyde), Methyl Octyl Acetaldehyde, aldehyde C-l l MOA (2-mehtyl deca-l-al), Onicidal (2,6,10- trimethyl-5,9-undecadien-l-al), Citronellyl oxyacetaldehyde, Muguet aldehyde 50 (3,7-dimethyl- 6-octenyl) oxyacetaldehyde), phenylacetaldehyde, Mefranal (3 -methyl-5 -phenyl pentanal), Triplal, Vertocitral dimethyl tetrahydrobenzene aldehyde (2,4-dimethyl-3-cyclohexene-l- carboxaldehyde), 2-phenylproprionaldehyde, Hydrotropaldehyde, Canthoxal, anisylpropanal 4- methoxy-alpha-methyl benzenepropanal (2-anisylidene propanal), Cylcemone A (1,2,3,4,5,6,7,8- octahydro-8,8-dimethyl-2-naphthaldehyde), and Precylcemone B (1-cyclohexene-l- carboxaldehyde) .

Still other exemplary aldehydes include, but are not limited to, acetaldehyde (ethanal), pentanal, valeraldehyde, amylaldehyde, Scentenal (octahydro-5-methoxy-4,7-Methano-lH- indene-2-carboxaldehyde), propionaldehyde (propanal), Cyclocitral, beta-cyclocitral, (2,6,6- trimethyl-l-cyclohexene-1 -acetaldehyde), Iso Cyclocitral (2,4,6-trimethyl-3-cyclohexene-l- carboxaldehyde), isobutyraldehyde, butyraldehyde, isovaleraldehyde (3-methyl butyraldehyde), methylbutyraldehyde (2-methyl butyraldehyde, 2-methyl butanal), Dihydrocitronellal (3,7- dimethyl octan-l-al), 2-Ethylbutyraldehyde, 3-Methyl-2-butenal, 2-Methylpentanal, 2-Methyl Valeraldehyde, Hexenal (2-hexenal, trans-2-hexenal), Heptanal, Octanal, Nonanal, Decanal, Laurie aldehyde, Tridecanal, 2-Dodecanal, Methylthiobutanal, Glutaraldehyde, Pentanedial, Glutaric aldehyde, Heptenal, cis or trans-Heptenal, Undecenal (2-, 10-), 2,4-octadienal, Nonenal (2-, 6-), Decenal (2-, 4-), 2,4-hexadienal, 2,4-Decadienal, 2,6-Nonadienal, Octenal, 2,6-dimethyl 5-heptenal, 2-isopropyl-5-methyl-2-hexenal, Trifernal, beta methyl Benzenepropanal, 2,6,6- Trimethyl-l-cyclohexene-l-acetaldehyde, phenyl Butenal (2 -phenyl 2-butenal), 2.Methyl-3(p- isopropylphenyl)-propionaldehyde, 3-(p-isopropylphenyl)-propionaldehyde, p-Tolylacetaldehyde (4-methylphenylacetaldehyde), Anisaldehyde (p-methoxybenzene aldehyde), Benzaldehyde, Vernaldehyde (l-Methyl-4-(4-methylpentyl)-3-cyclohexenecarbaldehyde), Heliotropin (piperonal) 3,4-Methylene dioxy benzaldehyde, alpha- Amylcinnamic aldehyde, 2-pentyl-3- phenylpropenoic aldehyde, Vanillin (4-methoxy 3 -hydroxy benzaldehyde), Ethyl vanillin (3- ethoxy 4-hydroxybenzaldehyde), Hexyl Cinnamic aldehyde, Jasmonal H (alpha-n-hexyl- cinnamaldehyde), Floralozone, (para-ethyl-alpha,alpha-dimethyl Hydrocinnamaldehyde), Acalea (p-methyl-alpha-pentylcinnamaldehyde), methylcinnamaldehyde, alpha-Methylcinnamaldehyde (2-methyl 3-pheny propenal), alpha-hexylcinnamaldehyde (2-hexyl 3-phenyl propenal), Salicylaldehyde (2 -hydroxy benzaldehyde), 4-ethyl benzaldehyde, Cuminaldehyde (4-isopropyl benzaldehyde), Ethoxybenzaldehyde, 2,4-dimethylbenzaldehyde, Veratraldehyde (3,4- dimethoxybenzaldehyde), Syringaldehyde (3,5-dimethoxy 4-hydroxybenzaldehyde), Catechaldehyde (3,4-dihydroxybenzaldehyde), Safranal (2,6,6-trimethyl-l,3-diene methanal), Myrtenal (pin-2-ene-l-carbaldehyde), Perillaldehyde L-4(l-methylethenyl)-l-cyclohexene-l- carboxaldehyde), 2,4-Dimethyl-3-cyclohexene carboxaldehyde, 2-Methyl-2-pentenal, 2- methylpentenal, pyruvaldehyde, formyl Tricyclodecan, Mandarin aldehyde, Cyclemax, Pino acetaldehyde, Corps Iris, Maceal, and Corps 4322.

In one embodiment, the malodor control component includes a mixture of two or more volatile aldehydes selected from the group consisting of 2-ethoxy Benzylaldehyde, 2-isopropyl- 5-methyl-2-hexenal, 5-methyl Furfural, 5-methyl-thiophene-carboxaldehyde, Adoxal, p- anisaldehyde, Benzylaldehyde, Bourgenal, Cinnamic aldehyde, Cymal, Decyl aldehyde, Floral super, Florhydral, Helional, Laurie aldehyde, Ligustral, Lyral, Melonal, o-anisaldehyde, Pino acetaldehyde, P.T. Bucinal, Thiophene carboxaldehyde, trans-4-Decenal, trans trans 2,4- Nonadienal, Undecyl aldehyde, and mixtures thereof.

In some embodiments, the malodor control component includes fast reacting volatile aldehydes. "Fast reacting volatile aldehydes" refers to volatile aldehydes that either (1) reduce amine odors by 20% or more in less than 40 seconds; or (2) reduce thiol odors by 20% or more in less than 30 minutes.

In one embodiment, the malodor control component includes a mixture of the volatile aldehydes listed in Table 1 and referred to herein as Accord A. Table 1

Figure imgf000015_0001

In another embodiment, the malodor control component includes a mixture of the volatile aldehydes listed in Table 2 and referred to herein as Accord B.

Table 2

Figure imgf000015_0002

In another embodiment, the malodor control component includes a mixture of about 71.2% volatile aldehydes, the remainder being other an ester and an alcohol perfume raw material. This mixture is listed in Table 3 and referred to herein as Accord C.

Table 3

Material Wt. % CAS Number ClogP VP (torr)

Group @25°C

Intreleven Aldehyde 2.000 112-45-8 3 0.060

Florhydral 10.000 125109-85-5 4 0.008

Floral Super 5.000 71077-31-1 3 0.030

Scentenal 2.000 86803-90-9 2 0.010

Cymal 15.000 103-95-7 4 0.007 Floralozone 12.000 67634-14-4 4 0.005

Adoxal 1.000 141-13-9 4 0.007

Methyl Nonyl

Acetaldehyde 1.000 110-41-8 3 0.030

Melonal 1.000 106-72-9 3 0.670

Flor Acetate 11.800 5413-60-5 1 0.060

Frutene 7.000 17511-60-3 4 0.020

Helional 5.000 1205-17-0 2 0.0005

Bourgeonal 2.000 18127-01-0 4 0.004

Linalool 10.000 78-70-6 3 0.050

Benzaldehyde 0.200 100-52-7 1 1.110

o-anisaldehyde 15.000 135-02-4 1 0.320

Accords A, B, or C can be formulated in with other perfume raw materials in an amount, for example, of about 10% by weight of the malodor control component. Additionally, the individual volatile aldehydes or a various combination of the volatile aldehydes can be formulated into a malodor control component. In certain embodiments, the volatile aldehydes may be present in an amount up to 100%, by weight of the malodor control component, alternatively from 1% to about 100%, alternatively from about 2% to about 100%, alternatively from about 3% to about 100%, alternatively about 50% to about 100%, alternatively about 70% to about 100%, alternatively about 80% to about 100%, alternatively from about 1% to about 20%, alternatively from about 1% to about 10%, alternatively from about 2% to about 20%, alternatively from about 3% to about 20%, alternatively from about 4% to about 20%, alternatively from about 5% to about 20%.

In some embodiments where volatility is not important for neutralizing a malodor, the present invention may include poly- aldehydes, for example, di-, tri-, tetra-aldehydes. Such embodiments may include laundry detergents, additive, and the like for leave-on, through the wash, and rinse-off type of applications.

In one embodiment, the freshening composition comprises a perfume mixture having one or more fabric-safe, non-yellowing aliphatic aldehydes. Certain types of aldehydes that predominately comprise a straight chain aliphatic backbone will not discolor fabrics, unlike products that utilize types of aldehydes that contain multiple double bonds and benzene rings. The following table illustrates the selection of aldehydes to avoid fabric yellowing.

Aldehyde Solution Tested Fadometer Test on treated Fabric

(0.75 grams of product are pipetted onto a 4 inch X 4 inch (10 cm X 10 cm)

swatch which is then subjected to 5 hours of exposure to simulated sunlight using a

SUNTEST CPS+ model Fadometer

supplied by Atlas, Chicago, Illinois,

USA.

Control- untreated fabric swatch No yellowing

1000 ppm amy lie cinnamic aldehyde Yellowish brown

(aromatic)

1000 ppm citronellal (aromatic) Yellowish brown

lOOOppm citral aldehyde (aliphatic) No yellowing

1000 ppm lauric aldehyde (aliphatic) No yellowing

Examples of suitable aliphatic aldehydes are R-COH where R is saturated C7 to C22 linear and/or branched with no more than two double bonds. Examples of suitable aliphatic aldehydes are bourgeonal, citral, citronellyl oxyacetaldehyde, cymal, decyl aldehyde, helional, hexyl cinnamic aldehyde, lauric aldehyde, ligustral, lyral, melonal, methyl dihydro jasmonate, methyl nonyl acetaldehyde, methyl phenyl carbinyl acetate, nonyl aldehyde, octyl aldehyde, oxane, P. T. bucinal, polysantol, rhubafuran, tripal, or mixtures thereof.

In one embodiment, the composition includes at least one aliphatic aldehyde selected from the group consisting of: bourgeonal, citral, citronellyl oxyacetaldehyde, cymal, decyl aldehyde, helional, hexyl cinnamic aldehyde, lauric aldehyde, ligustral, lyral, melonal, methyl dihydro jasmonate, methyl nonyl acetaldehyde, methyl phenyl carbinyl acetate, nonyl aldehyde, 2, 6 - nonadien-l-al, octyl aldehyde, oxane, P.T. bucinal, polysantol, rhubafuran, tripal, and mixtures thereof.

In another embodiment, the composition includes at least one aliphatic aldehyde selected from the group consisting of: burgeonal, cymal, hexyl cinnamic aldehyde, mmethyl dihydro jasmonate, methyl nonyl acetaldehyde, P.T. bucinal, and mixtures therof.

The aliphatic aldehydes may be present in an amount from about 0.001% to about 10%, alternatively from about 0.001% to about 5%, alternatively from about 0.01% to about 1%, alternatively from about 0.02% to about 1%, alternatively from about 0.02% to about 0.5%, alternatively from about 0.02% to about 0.06%, alternatively about 0.06%, by weight of the composition.

In addition to aliphatic aldehydes, the composition may also include perfume materials for their scent experience including enones, ketones, ionones including ionone alpha, ionone beta, ionone gamma methyl, or mixtures thereof. Suitable perfume materials are discussed in US 5,714,137. The composition may contain an effective amount of perfume to provide the freshening fragrance when first sprayed, some lingering fragrance, and some extra fragrance to be released upon fabric rewetting. It may be desirable for the aliphatic aldehydes to have virtually no negative impact on the desired perfume character.

Certain malodor counteractants may be odoriferous and negatively impact the overall character of the fragrance. In this case, a perfume/malodor counteractant premix is formed such that the perfume raw materials used are selected to neutralize any odor of the malodor counteractants. This odor neutralized premix can then be added to a parent perfume mixture without affecting the character of the parent fragrance. This permits the malodor counteractants to be used broadly with a large variety of fragrance types.

The following are non-limiting examples of perfume formulations that include fabric-safe malodor counteractants.

(1) Pine

Material Name Amount

Rosemary 10.00

Spike Lavender 10.00

Lavandin Grosso 5.00

Spruce (conf.-manh) 5.00

Camphor Gum 5.00

Melonal 0.30

Eucalyptol 15.00

Iso Menthone 15.00

Iso Bornyl Acetate 21.70

Ionone Beta 8.00

Iso E Super 5.00

100.00

(2) Ozonic

Material Name Amount

Xi Aldehyde 8.00

T 6 Nonadienol 10% In Dpg 5.00

Helional 13.00

Hydroxycitronellal 11.50

Calone 1951 0.50

T 6 - Nonadien-l-al/10% In Dpg 5.00

Lyral 20.00

Melonal 1.00 Iso Menthone 10.00

Floralozone 10.00

Bourgeonal 10.00

Delta Muscenone 962191 1.00

Habanolide 100% 5.00

100.00

(3) Fruity

Material Name Amount

Fruitate 5.00

Orange Terpenes 13.00

Ethyl Acetoacetate 3.00

T 6 Nonadienol 10% In Dpg 1.00

Ethyl Acetate 3.00

Benzaldehyde 2.00

Prenyl Acetate 8.00

Benzyl Acetate 15.00

T 6 - Nonadien-l-al/10% In Dpg 1.00

Ethyl-2-methyl Butyrate 8.00

Amyl Acetate 3.00

Cis 3 Hexenyl Acetate 3.00

Methyl Dihydro Jasmonate 10.00

Ligustral 5.00

Melonal 1.00

Ethyl 2 Methyl Pentanoate 8.00

Hexyl Acetate 8.00

Habanolide 100% 3.00

100.00

(4) Citrus

Material Name Amount

Orange Terpenes 20.00

Lemon Terpenes X5 Fold 20.00

Lime Oil Cf-8-1285-1 (conf.- berje) 10.00

Grapefruit Phase C- Ref. N* 12245 20.00

Italian Orange Phase Oil 22.90

Delta Muscenone 962191 0.50

Oxane 0.30 Iso Menthone 1.00

Rhubafuran 0.30

Habanolide 100% 5.00

100.00

(5) Floral

Material Name Amount

Spike Lavender 5.00

Rosemary 5.00

Helional 10.00

Hydroxycitronellal 10.00

Benzyl Acetate 9.30

Lyral 20.00

Ligustral 2.00

Melonal 0.20

Eucalyptol 2.00

Iso Menthone 8.00

Bourgeonal 20.00

Undecavertol 3.00

Delta Muscenone 962191 0.50

Habanolide 100% 5.00

100.00

In certain cases, fabrics that are laundered will have residual brighteners deposited from detergents with which they are washed. Therefore, it may be desirable for the aliphatic aldehydes to be compatible with brighteners so that the freshening composition will not discolor any fabrics with which it comes into contact. A number of the examples above are compatible with brighteners.

2. Perfume Delivery Systems

The malodor control component may include a perfume delivery system. The consumer who selects and uses such a perfumed product makes critical decisions as to how satisfied he or she is with the product at multiple touch points in the product usage profile. Although numerous touch points are known, Applicants have found that they can be advantageously grouped and expressed as three product moments of truth that are experienced by the typically consumer.

The FMOT is typically at the point of purchase, the SMOT typically begins with the product's application and use, and the TMOT typically begins immediately after the product's application and use. Applicants have recognized that a consumer's FMOT is negatively impacted because the product packaging inhibits the sensory experience; for example, product packaging may make the product difficult to open or, when open, exposes a product that can spill. In addition, formulation ingredients can suppress and/or distort neat product odor. Furthermore, Applicants have recognized that the consumer's SMOT is negatively impacted as volatile perfume raw materials are lost during product storage, resulting in reduced bloom during use. Compensating for these aforementioned deficiencies by adding high perfume levels for the TMOT can distort in-use scent experience, such that the perfume bloom can be too harsh or strong, and/or the perfume character can become less preferred. Also, Applicants have recognized that a consumer's FMOT is negatively impacted as perfume releases from the treated situs, inter alia a dry fabric over long period of time requires perfume levels in product that would distort the scent experience during the first and second moments of truth. Furthermore, addition of high perfume levels for SMOT & TMOT can distort neat product odor, and still not result in sufficient perfume deposition through the wash. In addition, perfume evaporation that occurs during drying can result in lower perfume levels on fabric; and/or the perfume remaining on dry fabric may provide initial dry fabric odor benefit but such perfume can dissipate too quickly to provide sufficient scent longevity benefits. Furthermore, perfume that is present on fabric may release too slowly from the fabric. As mentioned, the same can be the case with perfume delivery to and release from other situs such as hair and skin. The ability to notice the release of perfume can be impacted by a variety of factors such as hair length, clothing worn over skin, situs wash frequency, and the like. Furthermore, perfume intensity and/or character may be perceived differently on wet situs compared to dry situs that is treated with perfume-containing products. Without wishing to be bound by theory, in addition to loss of perfume by evaporation during drying, perfume can be made less available at certain touch points by being carried into or partitioning into the situs, such as cotton fibers, hair, skin, and the like. Situs moisture level can also serve to alter the release profile or release rate of perfume.

Finally, Applicants recognized that solutions to the problems that are associated with one or two moments of truth can be insufficient to resolve the problems associated with the remaining moment(s) of truth or negatively impact the other moment(s) of truth

The following perfume delivery technologies (PDTs) also known as perfume delivery systems may be used in any combination in any type of consumer product:

a. Polymer Assisted Delivery (PAD) This PDT uses polymeric materials to deliver perfume materials. Classical coacervation, water soluble or partly soluble to insoluble charged or neutral polymers, liquid crystals, hot melts, hydrogels, perfumed plastics, microcapsules, nano- and micro-latexes, polymeric film formers, and polymeric absorbents, polymeric adsorbents, etc. are some examples. PAD includes but is not limited to the following.

Matrix Systems: The fragrance is dissolved or dispersed in a polymer matrix or particle. Perfumes, for example, may be 1) dispersed into the polymer prior to formulating into the product or 2) added separately from the polymer during or after formulation of the product. Diffusion of perfume from the polymer is a common trigger that allows or increases the rate of perfume release from a polymeric matrix system that is deposited or applied to the desired surface (situs), although many other triggers are know that may control perfume release. Absorption and/or adsorption into or onto polymeric particles, films, solutions, and the like are aspects of this technology. Nano- or micro-particles composed of organic materials (e.g., latexes) are examples. Suitable particles include a wide range of materials including, but not limited to polyacetal, polyacrylate, polyacrylic, polyacrylonitrile, polyamide, polyaryletherketone, polybutadiene, polybutylene, polybutylene terephthalate, polychloroprene, poly ethylene, polyethylene terephthalate, polycyclohexylene dimethylene terephthalate, polycarbonate, polychloroprene, polyhydroxyalkanoate, polyketone, polyester, polyethylene, polyetherimide, polyethersulfone, polyethylenechlorinates, polyimide, polyisoprene, polylactic acid, polymethylpentene, polyphenylene oxide, polyphenylene sulfide, polyphthalamide, polypropylene, polystyrene, polysulfone, polyvinyl acetate, polyvinyl chloride, as well as polymers or copolymers based on acrylonitrile-butadiene, cellulose acetate, ethylene-vinyl acetate, ethylene vinyl alcohol, styrene -butadiene, vinyl acetate-ethylene, and mixtures thereof.

"Standard" systems refer to those that are "pre-loaded" with the intent of keeping the pre- loaded perfume associated with the polymer until the moment or moments of perfume release. Such polymers may also suppress the neat product odor and provide a bloom and/or longevity benefit depending on the rate of perfume release. One challenge with such systems is to achieve the ideal balance between 1) in-product stability (keeping perfume inside carrier until you need it) and 2) timely release (during use or from dry situs). Achieving such stability is particularly important during in-product storage and product aging. This challenge is particularly apparent for aqueous-based, surfactant-containing products, such as heavy duty liquid laundry detergents. Many "Standard" matrix systems available effectively become "Equilibrium" systems when formulated into aqueous-based products. One may select an "Equilibrium" system or a Reservoir system, which has acceptable in-product diffusion stability and available triggers for release (e.g., friction).

"Equilibrium" systems are those in which the perfume and polymer may be added separately to the product, and the equilibrium interaction between perfume and polymer leads to a benefit at one or more consumer touch points (versus a free perfume control that has no polymer-assisted delivery technology). The polymer may also be pre-loaded with perfume; however, part or all of the perfume may diffuse during in-product storage reaching an equilibrium that includes having desired perfume raw materials (PRMs) associated with the polymer. The polymer then carries the perfume to the surface, and release is typically via perfume diffusion. The use of such equilibrium system polymers has the potential to decrease the neat product odor intensity of the neat product (usually more so in the case of pre-loaded standard system). Deposition of such polymers may serve to "flatten" the release profile and provide increased longevity. As indicated above, such longevity would be achieved by suppressing the initial intensity and may enable the formulator to use more high impact or low odor detection threshold (ODT) or low Kovats Index (KI) PRMs to achieve FMOT benefits without initial intensity that is too strong or distorted. It is important that perfume release occurs within the time frame of the application to impact the desired consumer touch point or touch points. Suitable micro-particles and micro-latexes as well as methods of making same may be found in US 2005/0003980 Al. Matrix systems also include hot melt adhesives and perfume plastics. In addition, hydrophobically modified polysaccharides may be formulated into the perfumed product to increase perfume deposition and/or modify perfume release. All such matrix systems, including for example polysaccarides and nanolatexes may be combined with other PDTs, including other PAD systems such as PAD reservoir systems in the form of a perfume microcapsule (PMC). PAD matrix systems may include those described in the following references: U.S. Patent Publications: 2004/0110648 Al; 2004/0092414 Al; 2004/0091445 Al and 2004/0087476 Al; and US Patents: 6,531,444; 6,024,943; 6,042,792; 6,051,540; 4,540,721 and 4,973,422.

Silicones are also examples of polymers that may be used as PDT, and can provide perfume benefits in a manner similar to the polymer-assisted delivery "matrix system". Such a PDT is referred to as silicone-assisted delivery (SAD). One may pre-load silicones with perfume, or use them as an equilibrium system as described for PAD. Suitable silicones as well as making same may be found in WO 2005/102261; US 20050124530A1; US 20050143282A1; and WO 2003/015736. Functionalized silicones may also be used as described in US 2006/003913 Al. Examples of silicones include polydimethylsiloxane and poly alky ldimethylsiloxanes. Other examples include those with amine functionality, which may be used to provide benefits associated with amine-assisted delivery (AAD) and/or polymer- assisted delivery (PAD) and/or amine-reaction products (ARP). Other such examples may be found in US 4,911,852; US 2004/0058845 Al; US 2004/0092425 Al and US 2005/0003980 Al.

Reservoir Systems: Reservoir systems are also known as a core-shell type technology, or one in which the fragrance is surrounded by a perfume release controlling membrane, which may serve as a protective shell. The material inside the microcapsule is referred to as the core, internal phase, or fill, whereas the wall is sometimes called a shell, coating, or membrane. Microparticles or pressure sensitive capsules or microcapsules are examples of this technology. Microcapsules of the current invention are formed by a variety of procedures that include, but are not limited to, coating, extrusion, spray-drying, interfacial, in-situ and matrix polymerization. The possible shell materials vary widely in their stability toward water. Among the most stable are polyoxymethyleneurea (PMU)-based materials, which may hold certain PRMs for even long periods of time in aqueous solution (or product). Such systems include but are not limited to urea-formaldehyde and/or melamine-formaldehyde. Gelatin-based microcapsules may be prepared so that they dissolve quickly or slowly in water, depending for example on the degree of cross-linking. Many other capsule wall materials are available and vary in the degree of perfume diffusion stability observed. Without wishing to be bound by theory, the rate of release of perfume from a capsule, for example, once deposited on a surface is typically in reverse order of in-product perfume diffusion stability. As such, urea-formaldehyde and melamine-formaldehyde microcapsules for example, typically require a release mechanism other than, or in addition to, diffusion for release, such as mechanical force (e.g., friction, pressure, shear stress) that serves to break the capsule and increase the rate of perfume (fragrance) release. Other triggers include melting, dissolution, hydrolysis or other chemical reaction, electromagnetic radiation, and the like. The use of pre-loaded microcapsules requires the proper ratio of in-product stability and in- use and/or on-surface (on-situs) release, as well as proper selection of PRMs. Microcapsules that are based on urea-formaldehyde and/or melamine-formaldehyde are relatively stable, especially in near neutral aqueous-based solutions. These materials may require a friction trigger which may not be applicable to all product applications. Other microcapsule materials (e.g., gelatin) may be unstable in aqueous-based products and may even provide reduced benefit (versus free perfume control) when in-product aged. Scratch and sniff technologies are yet another example of PAD. Perfume microcapsules (PMC) may include those described in the following references: US Patent Publications: 2003/0125222 Al; 2003/215417 Al; 2003/216488 Al; 2003/158344 Al; 2003/165692 Al; 2004/071742 Al; 2004/071746 Al; 2004/072719 Al; 2004/072720 Al; 2006/0039934 Al; 2003/203829 Al; 2003/195133 Al; 2004/087477 Al; 2004/0106536 Al; and US Patents: 6,645,479 Bl; 6,200,949 Bl; 4,882,220; 4,917,920; 4,514,461; 6,106,875 and 4,234,627, 3,594,328 and US RE 32713.

b. Molecule- Assisted Delivery (MAD)

Non-polymer materials or molecules may also serve to improve the delivery of perfume. Without wishing to be bound by theory, perfume may non-covalently interact with organic materials, resulting in altered deposition and/or release. Non-limiting examples of such organic materials include but are not limited to hydrophobic materials such as organic oils, waxes, mineral oils, petrolatum, fatty acids or esters, sugars, surfactants, liposomes and even other perfume raw material (perfume oils), as well as natural oils, including body and/or other soils. Perfume fixatives are yet another example. In one aspect, non-polymeric materials or molecules have a CLogP greater than about 2. MAD may also include those described in US 7,119,060 and US 5,506,201.

c. Fiber- Assisted Delivery (FAD)

The choice or use of a situs itself may serve to improve the delivery of perfume. In fact, the situs itself may be a perfume delivery technology. For example, different fabric types such as cotton or polyester will have different properties with respect to ability to attract and/or retain and/or release perfume. The amount of perfume deposited on or in fibers may be altered by the choice of fiber, and also by the history or treatment of the fiber, as well as by any fiber coatings or treatments. Fibers may be woven and non- woven as well as natural or synthetic. Natural fibers include those produced by plants, animals, and geological processes, and include but are not limited to cellulose materials such as cotton, linen, hemp jute, flax, ramie, and sisal, and fibers used to manufacture paper and cloth. FAD may consist of the use of wood fiber, such as thermomechanical pulp and bleached or unbleached kraft or sulfite pulps. Animal fibers consist largely of particular proteins, such as silk, sinew, catgut and hair (including wool). Polymer fibers based on synthetic chemicals include but are not limited to polyamide nylon, PET or PBT polyester, phenol-formaldehyde (PF), polyvinyl alcohol fiber (PVOH), polyvinyl chloride fiber (PVC), polyolefins (PP and PE), and acrylic polymers. All such fibers may be pre-loaded with a perfume, and then added to a product that may or may not contain free perfume and/or one or more perfume delivery technologies. In one aspect, the fibers may be added to a product prior to being loaded with a perfume, and then loaded with a perfume by adding a perfume that may diffuse into the fiber, to the product. Without wishing to be bound by theory, the perfume may absorb onto or be adsorbed into the fiber, for example, during product storage, and then be released at one or more moments of truth or consumer touch points.

d. Amine Assisted Delivery (AAD)

The amine-assisted delivery technology approach utilizes materials that contain an amine group to increase perfume deposition or modify perfume release during product use. There is no requirement in this approach to pre-complex or pre-react the perfume raw material(s) and amine prior to addition to the product. In one aspect, amine-containing AAD materials suitable for use herein may be non-aromatic; for example, polyalkylimine, such as PEI, or PVam, or aromatic, for example, anthranilates. Such materials may also be polymeric or non-polymeric. In one aspect, such materials contain at least one primary amine. This technology will allow increased longevity and controlled release also of low ODT perfume notes (e.g., aldehydes, ketones, enones) via amine functionality, and delivery of other PRMs, without being bound by theory, via polymer-assisted delivery for polymeric amines. Without technology, volatile top notes can be lost too quickly, leaving a higher ratio of middle and base notes to top notes. The use of a polymeric amine allows higher levels of top notes and other PRMS to be used to obtain freshness longevity without causing neat product odor to be more intense than desired, or allows top notes and other PRMs to be used more efficiently. In one aspect, AAD systems are effective at delivering PRMs at pH greater than about neutral. Without wishing to be bound by theory, conditions in which more of the amines of the AAD system are deprotonated may result in an increased affinity of the deprotonated amines for PRMs such as aldehydes and ketones, including unsaturated ketones and enones such as damascone. In another aspect, polymeric amines are effective at delivering PRMs at pH less than about neutral. Without wishing to be bound by theory, conditions in which more of the amines of the AAD system are protonated may result in a decreased affinity of the protonated amines for PRMs such as aldehydes and ketones, and a strong affinity of the polymer framework for a broad range of PRMs. In such an aspect, polymer-assisted delivery may be delivering more of the perfume benefit; such systems are a subspecies of AAD and may be referred to as Amine- Polymer-Assisted Delivery or APAD. In some cases when the APAD is employed in a composition that has a pH of less than seven, such APAD systems may also be considered Polymer-Assisted Delivery (PAD). In yet another aspect, AAD and PAD systems may interact with other materials, such as anionic surfactants or polymers to form coacervate and/or coacervates-like systems. In another aspect, a material that contains a heteroatom other than nitrogen, for example sulfur, phosphorus or selenium, may be used as an alternative to amine compounds. In yet another aspect, the aforementioned alternative compounds can be used in combination with amine compounds. In yet another aspect, a single molecule may comprise an amine moiety and one or more of the alternative heteroatom moieties, for example, thiols, phosphines and selenols. Suitable AAD systems as well as methods of making same may be found in US Patent Applications 2005/0003980 Al; 2003/0199422 Al; 2003/0036489 Al; 2004/0220074 Al and USP 6,103,678.

e. Starch Encapsulated Accord (SEA)

The use of a starch encapsulated accord (SEA) technology allows one to modify the properties of the perfume, for example, by converting a liquid perfume into a solid by adding ingredients such as starch. The benefit includes increased perfume retention during product storage, especially under non-aqueous conditions. Upon exposure to moisture, a perfume bloom may be triggered. Benefits at other moments of truth may also be achieved because the starch allows the product formulator to select PRMs or PRM concentrations that normally cannot be used without the presence of SEA. Another technology example includes the use of other organic and inorganic materials, such as silica to convert perfume from liquid to solid. Suitable SEAs as well as methods of making same may be found in USPA 2005/0003980 Al and USP 6,458,754 Bl.

f. Zeolite & Inorganic Carrier (ZIC)

This technology relates to the use of porous zeolites or other inorganic materials to deliver perfumes. Perfume-loaded zeolite may be used with or without adjunct ingredients used for example to coat the perfume-loaded zeolite (PLZ) to change its perfume release properties during product storage or during use or from the dry situs. Suitable zeolite and inorganic carriers as well as methods of making same may be found in US Patent Publications: 2005/0003980 Al and US Patents: 5,858,959; 6,245,732 Bl; 6,048,830 and 4,539,135. Silica is another form of ZIC. Another example of a suitable inorganic carrier includes inorganic tubules, where the perfume or other active material is contained within the lumen of the nano- or micro-tubules. Preferably, the perfume-loaded inorganic tubule (or Perfume-Loaded Tubule or PLT) is a mineral nano- or micro-tubule, such as halloysite or mixtures of halloysite with other inorganic materials, including other clays. The PLT technology may also comprise additional ingredients on the inside and/or outside of the tubule for the purpose of improving in-product diffusion stability, deposition on the desired situs or for controlling the release rate of the loaded perfume. Monomeric and/or polymeric materials, including starch encapsulation, may be used to coat, plug, cap, or otherwise encapsulate the PLT. Suitable PLT systems as well as methods of making same may be found in US 5,651,976.

g. Pro-Perfume (PP)

This technology refers to perfume technologies that result from the reaction of perfume materials with other substrates or chemicals to form materials that have a covalent bond between one or more PRMs and one or more carriers. The PRM is converted into a new material called a pro-PRM (i.e., pro-perfume), which then may release the original PRM upon exposure to a trigger such as water or light. PP may provide enhanced perfume delivery properties such as increased perfume deposition, longevity, stability, retention, and the like. PP include those that are monomeric (non-polymeric) or polymeric, and may be pre-formed or may be formed in-situ under equilibrium conditions, such as those that may be present during in-product storage or on the wet or dry situs. Non-limiting examples of PP include Michael adducts (e.g., beta- amino ketones), aromatic or non-aromatic imines (Schiff bases), oxazolidines, beta-keto esters, and orthoesters. Another aspect includes compounds comprising one or more beta-oxy or beta-thio carbonyl moieties capable of releasing a PRM, for example, an alpha, beta-unsaturated ketone, aldehyde or carboxylic ester. The typical trigger for perfume release is exposure to water; although other triggers may include enzymes, heat, light, pH change, autoxidation, a shift of equilibrium, change in concentration or ionic strength and others. For aqueous-based products, light-triggered pro-perfumes are particularly suited. Such photo-pro-perfumes (PPPs) include but are not limited to those that release coumarin derivatives and perfumes and/or pro-perfumes upon being triggered. The released PP may release one or more PRMs by means of any of the above mentioned triggers. In one aspect, the PPP releases a nitrogen-based PP when exposed to a light and/or moisture trigger. In another aspect, the nitrogen-based PP, released from the PPP, releases one or more PRMs selected, for example, from aldehydes, ketones (including enones) and alcohols. In still another aspect, the PPP releases a dihydroxy coumarin derivative. The light- triggered pro-perfume may also be an ester that releases a coumarin derivative and a perfume alcohol. In one aspect the pro-perfume is a dimethoxybenzoin derivative as described in US 2006/0020459 Al. In another aspect, the PP is a 3', 5 '-dimethoxybenzoin (DMB) derivative that releases an alcohol upon exposure to electromagnetic radiation. In yet another aspect, the pro- perfume releases one or more low ODT PRMs, including tertiary alcohols such as linalool, tetrahydrolinalool, or dihydromyrcenol. Suitable pro-perfumes and methods of making same can be found in US Patents: 7,018,978 B2; 6,987,084 B2; 6,956,013 B2; 6,861,402 Bl; 6,544,945 Bl; 6,093,691; 6,277,796 Bl; 6,165,953; 6,316,397 Bl; 6,437,150 Bl; 6,479,682 Bl; 6,096,918; 6,218,355 Bl; 6,133,228; 6,147,037; 7,109,153 B2; 7,071,151 B2; 6,987,084 B2; 6,610,646 B2 and 5,958,870, as well as can be found in US Patent Publications: 2005/0003980 Al and 2006/0223726 Al.

Amine Reaction Product (ARP): For purposes of the present application, ARP is a subclass or species of PP. One may also use "reactive" polymeric amines in which the amine functionality is pre-reacted with one or more PRMs to form an amine reaction product (ARP). Typically the reactive amines are primary and/or secondary amines, and may be part of a polymer or a monomer (non-polymer). Such ARPs may also be mixed with additional PRMs to provide benefits of polymer-assisted delivery and/or amine-assisted delivery. Nonlimiting examples of polymeric amines include polymers based on polyalkylimines, such as PEI, or PVam. Nonlimiting examples of monomeric (non-polymeric) amines include hydroxyl amines, such as 2-aminoethanol and its alkyl substituted derivatives, and aromatic amines such as anthranilates. The ARPs may be premixed with perfume or added separately in leave-on or rinse-off applications. In another aspect, a material that contains a heteroatom other than nitrogen, for example oxygen, sulfur, phosphorus or selenium, may be used as an alternative to amine compounds. In yet another aspect, the aforementioned alternative compounds can be used in combination with amine compounds. In yet another aspect, a single molecule may comprise an amine moiety and one or more of the alternative heteroatom moieties, for example, thiols, phosphines and selenols. The benefit may include improved delivery of perfume as well as controlled perfume release. Suitable ARPs as well as methods of making same can be found in US 2005/0003980 Al and US 6,413,920 Bl.

3. Low molecular weight polyols

In addition to perfume materials, the malodor control component may include low molecular weight polyols with relatively high boiling points (compared to water) such as ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, and/or glycerine. Such polyols may improve odor neutralization of the composition of the present invention. Some polyols, e.g., dipropylene glycol, are also useful to facilitate the solubilization of some perfume ingredients in the composition of the present invention.

The glycol used in the composition of the present invention may be glycerine, ethylene glycol, propylene glycol, dipropylene glycol, polyethylene glycol, propylene glycol methyl ether, propylene glycol phenyl ether, propylene glycol methyl ether acetate, propylene glycol n-butyl ether, dipropylene glycol n-butyl ether, dipropylene glycol n-propyl ether, ethylene glycole phenyl ether, diethylene glycol n-butyl ether, dipropylene glycol n-butyl ether, diethylene glycol mono butyl ether, dipropylene glycol methyl ether, tripropylene glycol methyl ether, tripropylene glycol n-butyl ether, other glycol ethers, or mixtures thereof. In one embodiment, the glycol used is ethylene glycol, propylene glycol, or mixtures thereof. In another embodiment, the glycol used is diethylene glycol.

Typically, the low molecular weight polyol is added to the composition of the present invention at a level of from about 0.01% to about 5%, by weight of the composition, alternatively from about 0.05% to about 1%, alternatively from about 0.1% to about 0.5%, by weight of the composition. Compositions with higher concentrations may make fabrics susceptible to soiling and/or leave unacceptable visible stains on fabrics as the solution evaporates off of the fabric. The weight ratio of low molecular weight polyol to the malodor binding polymer is from about 500:1 to about 4:1, alternatively from about 1:100 to about 25:1, alternatively from about 1:50 to about 4:1, alternatively about 4:1.

4. Cyclodextrin

In some embodiments, the freshening composition may include solubilized, water- soluble, uncomplexed cyclodextrin. As used herein, the term "cyclodextrin" includes any of the known cyclodextrins such as unsubstituted cyclodextrins containing from six to twelve glucose units, especially, alpha-cyclodextrin, beta-cyclodextrin, gamma-cyclodextrin and/or their derivatives and/or mixtures thereof. The alpha-cyclodextrin consists of six glucose units, the beta-cyclodextrin consists of seven glucose units, and the gamma-cyclodextrin consists of eight glucose units arranged in a donut-shaped ring. The specific coupling and conformation of the glucose units give the cyclodextrins a rigid, conical molecular structure with a hollow interior of a specific volume. The "lining" of the internal cavity is formed by hydrogen atoms and glycosidic bridging oxygen atoms, therefore this surface is fairly hydrophobic. The unique shape and physical-chemical property of the cavity enable the cyclodextrin molecules to absorb (form inclusion complexes with) organic molecules or parts of organic molecules which can fit into the cavity. Many perfume molecules can fit into the cavity.

Cyclodextrin molecules are described in US 5,714,137, and US 5,942,217. Suitable levels of cyclodextrin are from about 0.1% to about 5%, alternatively from about 0.2% to about 4%, alternatively from about 0.3% to about 3%, alternatively from about 0.4% to about 2%, by weight of the freshening composition. Freshening compositions with higher concentrations can make fabrics susceptible to soiling and/or leave unacceptable visible stains on fabrics as the solution evaporates off of the fabric. The latter is especially a problem on thin, colored, synthetic fabrics. In order to avoid or minimize the occurrence of fabric staining, the fabric may be treated at a level of less than about 5 mg of cyclodextrin per mg of fabric, alternatively less than about 2 mg of cyclodextrin per mg of fabric.

5. Acid Catalyst

The malodor control component of the present invention may include an effective amount of an acid catalyst to neutralize sulfur-based malodors. It has been found that certain mild acids have an impact on aldehyde reactivity with thiols in the liquid and vapor phase. It has been found that the reaction between thiol and aldehyde is a catalytic reaction that follows the mechanism of hemiacetal and acetal formation path. When the present malodor control component contains an acid catalyst and contacts a sulfur-based malodor, the volatile aldehyde reacts with thiol. This reaction may form a thiol acetal compound, thus, neutralizing the sulfur- based odor. Without an acid catalyst, only hemi-thiol acetal is formed.

Suitable acid catalysts have a VP, as reported by Scifinder, in the range of about 0.001 torr to about 38 torr, measured at 25 °C, alternatively about 0.001 torr to about 14 torr, alternatively from about 0.001 to about 1, alternatively from about 0.001 to about 0.020, alternatively about 0.005 to about 0.020, alternatively about 0.010 to about 0.020.

The acid catalyst may be a weak acid. A weak acid is characterized by an acid dissociation constant, Ka> which is an equilibrium constant for the dissociation of a weak acid; the pKa being equal to minus the decimal logarithm of Ka. The acid catalyst may have a pKa from about 4.0 to about 6.0, alternatively from about 4.3 and 5.7, alternatively from about 4.5 to about 5, alternatively from about 4.7 to about 4.9. Suitable acid catalyst include those listed in Table 4.

Table 4

Figure imgf000031_0001

Depending on the desired use of the malodor control component, one may consider the scent character or the affect on the scent of the malodor control component when selecting an acid catalyst. In some embodiments of the malodor control component, it may be desirable to select an acid catalyst that provides a neutral to pleasant scent. Such acid catalysts may have a VP of about 0.001 torr to about 0.020 torr, measured at 25 °C, alternatively about 0.005 torr to about 0.020 torr, alternatively about 0.010 torr to about 0.020 torr. Non-limiting examples of such acid catalyst include 5-methyl thiophene carboxaldehyde with carboxylic acid impurity, succinic acid, or benzoic acid.

The malodor control component may include about 0.05% to about 5%, alternatively about 0.1% to about 1.0%, alternatively about 0.1% to about 0.5%, alternatively about 0.1% to about 0.4%, alternatively about 0.4% of an acid catalyst by weight of the malodor control component.

In an acetic acid system, the present malodor control component may include about 0.4% of acetic acid (50:50 TC:DPM, 0.4% acetic acid).

Table 5

Figure imgf000032_0001

The malodor control component may have a pH from about 3 to about 8, alternatively from about 4 to about 7, alternatively from about, alternatively from about 4 to about 6.

6. Optional Ingredients

The malodor control component may, optionally, include odor masking agents, and/or odor blocking agents. "Odor blocking" refers to the ability of a compound to dull the human sense of smell. "Odor-masking" refers to the ability of a compound to mask or hide a malodorous compound. Odor-masking may include a compound with a non-offensive or pleasant smell that is dosed such that it limits the ability to sense a malodorous compound. Odor- masking may involve the selection of compounds which coordinate with an anticipated malodor to change the perception of the overall scent provided by the combination of odorous compounds.

The malodor control component may also, optionally, include perfume raw materials that solely provide a hedonic benefit (i.e. that do not neutralize malodors yet provide a pleasant fragrance). Suitable perfumes are disclosed in US 6,248,135, which is incorporated in its entirety by reference.

For example, the malodor control component may include a mixture of volatile aldehydes for neutralizing a malodor, perfume ionones, and a diluent. Alternatively, the malodor control component may include 100% volatile aldehydes.

C. Buffering agent

The freshening composition of the present invention includes a buffering agent which may be a dibasic acid, carboxylic acid, or a dicarboxylic acid like maleic acid. The acid may be sterically stable, and used in this composition solely for maintaining the desired pH. The freshening composition may have a pH from about 3 to about 8, alternatively from about 4 to about 7, alternatively from about 5 to about 8, alternatively from about 6 to about 8, alternatively about 6 to about 7, alternatively about 7, alternatively about 6.5.

Carboxylic acids such as citric acid may act as metal ion chelants and can form metallic salts with low water solubility. As such, in some embodiments, the freshening composition is essentially free of citric acids. The buffer can be alkaline, acidic or neutral.

Other suitable buffering agents for freshening compositions of this invention include biological buffering agents. Some examples are nitrogen-containing materials, sulfonic acid buffers like 3-(N-morpholino)propanesulfonic acid (MOPS) or N-(2-Acetamido)-2- aminoethanesulfonic acid (ACES), which have a near neutral 6.2 to 7.5 pKa and provide adequate buffering capacity at a neutral pH. Other examples are amino acids such as lysine or lower alcohol amines like mono-, di-, and tri-ethanolamine. Other nitrogen-containing buffering agents are tri(hydroxymethyl)amino methane (HOCH2)3CNH3 (TRIS), 2-amino-2-ethyl-l,3- propanediol, 2-amino-2-methyl-propanol, 2-amino-2-methyl-l,3-propanol, disodium glutamate, N-methyl diethanolamide, 2-dimethylamino-2-methylpropanol (DMAMP), 1,3- bis(methylamine)-cyclohexane, 1,3-diamino-propanol Ν,Ν'-tetra- methyl- l,3-diamino-2- propanol, N,N-bis(2-hydroxyethyl)glycine (bicine) and N-tris (hydroxymethyl)methyl glycine (tricine). Mixtures of any of the above are also acceptable.

The compositions may contain at least about 0%, alternatively at least about 0.001%, alternatively at least about 0.01%, by weight of the composition, of a buffering agent. The composition may also contain no more than about 1%, alternatively no more than about 0.75%, alternatively no more than about 0.5%, by weight of the composition, of a buffering agent.

D. Solubilizer The freshening composition of the present invention may contain a diluent or solubilizing aid to solubilize any excess hydrophobic organic materials, particularly any perfume materials, and also optional ingredients (e.g., insect repelling agent, antioxidant, etc.) which can be added to the composition, that are not readily soluble in the composition, to form a clear solution. Exemplary solubilizing aids include such as a no-foaming or low-foaming surfactants, nonionic surfactants, cationic surfactants, amphoteric surfactants, zwitterionic surfactants, and mixtures thereof. Exemplary solubilizing aids also include dipropylene glycol methyl ether, 3-methoxy-3- methyl-l-butanol, and mixtures thereof

In some embodiments, the composition contains nonionic surfactants, cationic surfactants, and mixtures thereof. In one embodiment, the freshening composition contains hydrogenated castor oil. One suitable hydrogenated castor oil that may be used in the present composition is Basophor™, available from BASF.

Compositions containing anionic surfactants and/or detergent surfactants may make fabrics susceptible to soiling and/or leave unacceptable visible stains on fabrics as the solution evaporates off of the fabric. In some embodiments, the freshening composition is free of anionic surfactants and/or detergent surfactants.

When the solubilizing agent is present, it is typically present at a level of from about 0.01% to about 3%, alternatively from about 0.05% to about 1%, alternatively from about 0.01% to about 0.05%, by weight of the freshening composition. Freshening compositions with higher concentrations may make fabrics susceptible to soiling and/or leave unacceptable visible stains on fabrics as the solution evaporates off of the fabric.

E. Antimicrobial Compounds

The freshening composition of the present invention may include an effective amount of a compound for reducing microbes in the air or on inanimate surfaces. Antimicrobial compounds are effective on gram negative and gram positive bacteria and fungi typically found on indoor surfaces that have contacted human skin or pets such as couches, pillows, pet bedding, and carpets. Such microbial species include Klebsiella pneumoniae, Staphylococcus aureus, Aspergillus niger, Klebsiella pneumoniae, Steptococcus pyogenes, Salmonella choleraesuis, Escherichia coil, Trichophyton mentagrophytes, and Pseudomonoas aeruginosa. In some embodiments, the antimicrobial compounds are also effective on viruses such Hl-Nl, Rhinovirus, Respiratory Syncytial, Poliovirus Type 1, Rotavirus, Influenza A, Herpes simplex types 1 & 2, Hepatitis A, and Human Coronavirus. Antimicrobial compounds suitable in the composition of the present invention can be any organic material which will not cause damage to fabric appearance (e.g., discoloration, coloration such as yellowing, bleaching). Water-soluble antimicrobial compounds include organic sulfur compounds, halogenated compounds, cyclic organic nitrogen compounds, low molecular weight aldehydes, quaternary compounds, dehydroacetic acid, phenyl and phenoxy compounds, or mixtures thereof.

In one embodiment, a quaternary compound is used. Examples of commercially available quaternary compounds suitable for use in the freshening composition is Barquat available from Lonza Corporation; and didecyl dimethyl ammonium chloride quat under the trade name Bardac® 2250 from Lonza Corporation.

The antimicrobial compound may be present in an amount from about 500 ppm to about 7000 ppm, alternatively about 1000 ppm to about 5000 ppm, alternatively about 1000 ppm to about 3000 ppm, alternatively about 1400 ppm to about 2500 ppm, by weight of the freshening composition.

F. Preservatives

The composition of the present invention may include a preservative. The preservative is included in the present invention in an amount sufficient to prevent spoilage or prevent growth of inadvertently added microorganisms for a specific period of time, but not sufficient enough to contribute to the odor neutralizing performance of the freshening composition. In other words, the preservative is not being used as the antimicrobial compound to kill microorganisms on the surface onto which the composition is deposited in order to eliminate odors produced by microorganisms. Instead, it is being used to prevent spoilage of the composition in order to increase the shelf-life of the composition.

The preservative can be any organic preservative material which will not cause damage to fabric appearance, e.g., discoloration, coloration, bleaching. Suitable water-soluble preservatives include organic sulfur compounds, halogenated compounds, cyclic organic nitrogen compounds, low molecular weight aldehydes, parabens, propane diaol materials, isothiazolinones, quaternary compounds, benzoates, low molecular weight alcohols, dehydroacetic acid, phenyl and phenoxy compounds, or mixtures thereof.

Non-limiting examples of commercially available water-soluble preservatives for use in the present invention include a mixture of about 77% 5-chloro-2-methyl-4-isothiazolin-3-one and about 23% 2-methyl-4-isothiazolin-3-one, a broad spectrum preservative available as a 1.5% aqueous solution under the trade name Kathon® CG by Rohm and Haas Co.; 5-bromo-5-nitro- 1,3-dioxane, available under the tradename Bronidox L® from Henkel; 2-bromo-2-nitropropane- 1,3-diol, available under the trade name Bronopol® from Inolex; Ι,Γ-hexamethylene bis(5-(p- chlorophenyl)biguanide), commonly known as chlorhexidine, and its salts, e.g., with acetic and digluconic acids; a 95:5 mixture of l,3-bis(hydroxymethyl)-5,5-dimethyl-2,4-imidazolidinedione and 3-butyl-2-iodopropynyl carbamate, available under the trade name Glydant Plus® from Lonza; N-[l,3-bis(hydroxymethyl)2,5-dioxo-4-imidazolidinyl]-N,N'-bis(hydroxy-methyl) urea, commonly known as diazolidinyl urea, available under the trade name Germall® II from Sutton Laboratories, Inc.; N,N"-methylenebis{N'-[l-(hydroxymethyl)-2,5-dioxo-4-imidazolidinyl]urea}, commonly known as imidazolidinyl urea, available, e.g., under the trade name Abiol® from 3V- Sigma, Unicide U-13® from Induchem, Germall 115® from Sutton Laboratories, Inc.; polymethoxy bicyclic oxazolidine, available under the trade name Nuosept® C from Huls America; formaldehyde; glutar aldehyde; polyaminopropyl biguanide, available under the trade name Cosmocil CQ® from ICI Americas, Inc., or under the trade name Mikrokill® from Brooks, Inc; dehydroacetic acid; and benzsiothiazolinone available under the trade name Koralone™ B - 119 from Rohm and Hass Corporation.

Suitable levels of preservative are from about 0.0001% to about 0.5%, alternatively from about 0.0002% to about 0.2%, alternatively from about 0.0003% to about 0.1%, by weight of the freshening composition.

G. Wetting Agent

The composition may include a wetting agent that provides a low surface tension that permits the composition to spread readily and more uniformly on hydrophobic surfaces like polyester and nylon. It has been found that the aqueous solution, without such a wetting agent will not spread satisfactorily. The spreading of the composition also allows it to dry faster, so that the treated material is ready to use sooner. Furthermore, a composition containing a wetting agent may penetrate hydrophobic, oily soil better for improved malodor neutralization. A composition containing a wetting agent may also provide improved "in-wear" electrostatic control. For concentrated compositions, the wetting agent facilitates the dispersion of many actives such as antimicrobial actives and perfumes in the concentrated aqueous compositions.

Nonlimiting examples of wetting agents include block copolymers of ethylene oxide and propylene oxide. Suitable block polyoxyethylene-polyoxypropylene polymeric surfactants include those based on ethylene glycol, propylene glycol, glycerol, trimethylolpropane and ethylenediamine as the initial reactive hydrogen compound. Polymeric compounds made from a sequential ethoxylation and propoxylation of initial compounds with a single reactive hydrogen atom, such as C12-I8 aliphatic alcohols, are not generally compatible with the cyclodextrin.

Certain of the block polymer surfactant compounds designated Pluronic® and Tetronic® by the BASF- Wyandotte Corp., Wyandotte, Michigan, are readily available.

Nonlimiting examples of cyclodextrin-compatible wetting agents of this type are described in US 5,714,137 and include the Silwet® surfactants available from Momentive

Performance Chemical, Albany, New York. Exemplary Silwet surfactants are as follows

Name Average MW

L-7608 600

L-7607 1,000

L-77 600

L-7605 6,000

L-7604 4,000

L-7600 4,000

L-7657 5,000

L-7602 3,000;

and mixtures thereof.

H. Aqueous carrier

The composition of the present invention may include an aqueous carrier. The aqueous carrier which is used may be distilled, deionized, or tap water. Water may be present in any amount for the composition to be an aqueous solution. In some embodiments, water may be present in an amount of about 85% to 99.5%, alternatively about 90% to about 99.5%, alternatively about 92% to about 99.5%, alternatively about 95%, by weight of said freshening composition. Water containing a small amount of low molecular weight monohydric alcohols, e.g., ethanol, methanol, and isopropanol, or polyols, such as ethylene glycol and propylene glycol, can also be useful. However, the volatile low molecular weight monohydric alcohols such as ethanol and/or isopropanol should be limited since these volatile organic compounds will contribute both to flammability problems and environmental pollution problems. If small amounts of low molecular weight monohydric alcohols are present in the composition of the present invention due to the addition of these alcohols to such things as perfumes and as stabilizers for some preservatives, the level of monohydric alcohol may be less than about 6%, alternatively less than about 3%, alternatively less than about 1%, by weight of the freshening composition.

I. Other Optional ingredients Adjuvants can be optionally added to the freshening composition herein for their known purposes. Such adjuvants include, but are not limited to, water soluble metallic salts, antistatic agents, insect and moth repelling agents, colorants, antioxidants, and mixtures thereof. II. Method of Making

The composition can be made in any suitable manner known in the art. All of the ingredients can simply be mixed together. In certain embodiments, it may be desirable to make a concentrated mixture of ingredients and dilute by adding the same to an aqueous carrier before dispersing the composition into the air or on an inanimate surface. In another embodiment, the malodor binding polymer may be dispersed in one vessel containing deionized water and ethanol, and low molecular polyols. To this vessel, then, the buffer is added until fully dispersed and visually dissolved. In a separate vessel, the solubilizer and perfume are mixed until homogenous. The solution of solubilizer and perfume are then added to the first mixing vessel, and mixed until homogenous.

III. Methods of Use

The freshening composition of the present invention can be used by dispersing, e.g., by placing the aqueous solution into a dispensing means, such as a spray dispenser and spraying an effective amount into the air or onto the desired surface or article. An effective amount as defined herein means an amount sufficient to neutralize malodor to the point that it is not discernible by the human sense of smell yet not so much as to saturate or create a pool of liquid on an article or surface and so that, when dry, there is no visual deposit readily discernible.

Dispersing can be achieved by using a spray device, a roller, a pad, etc.

The present invention encompasses the method of dispersing an effective amount of the composition for reducing malodor onto household surfaces. The household surfaces are selected from the group consisting of countertops, cabinets, walls, floors, bathroom surfaces, and kitchen surfaces.

The present invention encompasses the method of dispersing a mist of an effective amount of the composition for reducing malodor onto fabric and/or fabric articles. The fabric and/or fabric articles include, but are not limited to, clothes, curtains, drapes, upholstered furniture, carpeting, bed linens, bath linens, tablecloths, sleeping bags, tents, car interior, e.g., car carpet, fabric car seats, etc. The present invention encompasses the method of dispersing a mist of an effective amount of the composition for reducing malodor impression onto and into shoes wherein the shoes are not sprayed to saturation.

The present invention encompasses the method of dispersing a mist of an effective amount of the composition for reducing malodor impression onto shower curtains.

The present invention relates to the method of dispersing a mist of an effective amount of the composition for reducing malodor impression onto and/or into garbage cans and/or recycling bins.

The present invention relates to the method of dispersing a mist of an effective amount of the composition for reducing malodor impression into the air to neutralize malodor.

The present invention relates to the method of dispersing a mist of an effective amount of the composition for reducing malodor impression into and/or onto major household appliances including, but not limited to, refrigerators, freezers, washing machines, automatic dryers, ovens, microwave ovens, dishwashers, etc., to neutralize malodor.

The present invention relates to the method of dispersing a mist of an effective amount of the composition for reducing malodor impression onto cat litter, pet bedding and pet houses to neutralize malodor.

The present invention relates to the method of dispersing a mist of an effective amount of the composition for reducing malodor impression onto household pets to neutralize malodor.

EXAMPLES

Malodor Reduction

Table 6 show non-limiting examples of freshening compositions according to the present invention.

Table 6

I II III IV V VI VII VIII

(Control

)

Lupasol WF 0.070 0.070 0.015 0.035 0 0.035 0.0525 0.07 CAS 9002-98-6

Diethylene 0.175 0.175 0.070 0.175 0.175 0.175 0.170 0.175 Glycol

Perfume mixture 0.2102 0.4880 0.020 0.236 0.655 0.655 0.655 0.655 comprising (0% (0.012 (0.012 (0.012 (0.012 aliphatic aldealdealdealdealdealdehydes hydes) hydes) hydes) hydes) hydes)

Hydroxypropyl 0.630 0.630 0.630 0 0.630 0.630 0.630 0.630 Beta CD

Basophor ELH 0 0.050 0.050 0.050 0.050 0.050 0.050 0.050 60

Uniquat 2250 0 0.060 0 0.060 0.060 0.060 0.060 0.060

Bardac 2250J 0.139 0.100 0 0 0 0 0

Silwet L-7600 0.100 0.100 0.175 0.100 0.100 0.100 0.100 0.100

Citric Acid 0.045 0.015 0.015 0.015 0.015 0.015 0.15 0.015

Maleic Acid 0 0.050 0.060 0.050 0.050 0.050 0.050 0.050 CAS 110-16-7

ACES 0.100 0 0 0 0 0 0 0

Sodium 0 0 0 0.020 0.020 0.020 0.020 0.020 Hydroxide

Koralone B-119 0 0.0150 0 0.015 0.015 0.015 0.015 0.015

Ethanol 3.000 3.000 3.000 3.000 3.000 3.000 3.000 3.000

Deionized 95.571 95.347 95.865 96.264 95.318 95.180 95.095 95.148 Water

Total 100 100 100 100 100

Formulations VI, VII, and VIII in Table 6 are prepared and compared to Control Formulation V, a composition containing no malodor binding polymer, for their effect on malodor. Fig. 1 shows that when including a malodor binding polymer in a freshening composition in accordance with the present invention, aldehydic malodor evaporating off the treated fabric decreases.

Fabric samples are infused with the malodor of interest. For grease infusion, place 8 ounces of grease in a Presto™ electric skillet and cover with the skillet lid. Place the skillet in a 30 gallon metal garbage can. Run the electric cord from the skillet through a 1.5 inch hole in the garbage can. Heat the skillet to 121°C and allow it to equilibrate for 15 minutes. Remove the lid. Suspend 8 inch by 8 inch fabric swatches from the metal clips on a carousel in the garbage can lid. Measured from the bottom of the swatches, the distance to the top of the skillet is 8 inches. Place lid on garbage can and manually turn the carousel 15 rotations per minute for a period of 40 minutes. After infusion, spray the swatches with the respective freshening compositions that are to be tested. The spray for each swatch consists of two full strokes of the trigger sprayer bottle. The bottle is held 6 inches away from the fabric and the spray is centered on the fabric. Immediately after treatment, cut each swatch in half, roll, and place each into a 125 mL headspace vial. Seal the vials. Allow the vials to equilibrate for at least 2 hours at 100 °C and then analyze by sampling each vial using a PDMS SPME fiber and analyze by GC/MS. Malodor components, previously identified, are then tracked through all the samples. Data is compiled of total area count of the cumulative area counts of the individual peaks.

Microbe Reduction

Table 7 show non-limiting examples of freshening compositions according to the present invention.

Table 7

Figure imgf000041_0001

Formulation IX, the control formulation containing no malodor binding polymer, and Formulation X are compared for their effect on microbe reduction. Fig. 2 shows the results of formulations with and without PEIs when tested for non-residual fabric sanitizer efficacy against Staphylococcus aureus (ATCC 6538), Aspergillus niger (ATCC 6275), Proteus mirabilis (ATCC 7002) and Pseudomonas aeruginosa (ATCC 15442).

Formulation efficacy was assessed by employing a North American Bactericidal Fabric Spray Test Method that is a quantitative modification of the AO AC Germicidal Spray Products Test method (961.02). This method is a recognized test standard in accordance to U.S. EPA Pesticide Assessment Guidelines Subdivision G, Series 91-52(b)(l). The referenced AOAC method was applied to fabric surfaces. Fabric swatches (1.5 inch, 100% blue oxford cotton) as can be obtained from Testfabrics Inc. were treated with 2 fully depressed sprays of trigger sprayer bottle containing the respective formulation. A contact time between 10 to 30 minutes at ambient temperature was chosen as a conservative time estimate for sprayed fabric surfaces, as provided in Subdivision G, Series 91-1 (b) (4) (i). Any excess liquid is drained off and then transferred to a jar containing 20 ml neutralizer and/or growth promoting broth. The jar is mixed by vortexing, followed by sonication in a Branson Bransonic Ultrasonic Sonicator for 5 minutes. Within 30 minutes of neutralization, the jar is mixed for 2-3 seconds on a vortex type mixer and serially diluted. All the samples were incubated (48 + 4 hours) under the appropriate conditions and monitored for growth or no growth. Samples are plated and counted to determine mean loglO reduction.

Effect of volatile aldehydes on amine-based and sulfur-based malodors

Malodor standards are prepared by pipeting 1 mL of butylamine (amine-based malodor) and butanethiol (sulfur-based malodor) into a 1.2 liter gas sampling bag. The bag is then filled to volume with nitrogen and allowed to sit for at least 12 hours to equilibrate.

A 1 μΕ sample of each volatile aldehyde listed in Table 6 and each Accord (A, B, and C) listed in Tables 1 to 3 is pipeted into individual 10 mL silanized headspace vials. The vials are sealed and allowed to equilibrate for at least 12 hours. Repeat 4 times for each sample (2 for butylamine analysis and 2 for butanethiol analysis).

After the equilibration period, 1.5 mL of the target malodor standard is injected into each vial containing a volatile aldehyde or Accord sample. For thiol analysis, the samples are held at room temperature for 30 minutes prior to injection into the system. A 1 mL headspace syringe is used to inject 250 μΐ^ of each sample into the system for the thiol samples. For amine analysis, the samples are injected immediately into the system after the malodor is introduced. A 1 mL headspace syringe is used to inject 500 μΐ^ of each sample into the system for the amine samples.

A GC pillow is used for the amine analysis to shorten the run times. Samples are then analyzed using a GC/MS with a DB-5, 20 m, 1 μηι film thickness column with an MPS-2 autosampler equipment with static headspace function. Data is analyzed by ion extraction on each total ion current current (56 for thiol - 30 for amine) and the area is used to calculate the percent reduction from the malodor standard for each sample. Table 8 shows the effect of certain volatile aldehydes on neutralizing amine-based and sulfur based malodors at 40 seconds and 30 minutes, respectively.

Table 8

Perfume Raw Material (R-CHO) At least 20% At least 20%

butylamine butanethiol reduction at 40 reduction at 30 seconds? minutes?

2,4,5 Trimethoxy Benzaldehyde No No

2,4, 6-Trimethoxy-benzylaldehyde No No

2-ethoxy benzylaldehyde Yes Yes

2-isopropyl-5-methyl-2-hexenal Yes Yes

2-methyl-3-(2-furyl)-propenal No No

3,4,5 Trimethoxy Benzaldehyde No No

3 ,4-Trimethoxy-benzylaldehyde No No

4-tertbutyl benzylaldehyde Yes No

5 -methyl furfural Yes Yes

5-methyl-thiophene-carboxaldehyde No Yes

Adoxal Yes No

Amyl cinnamic aldehyde No No

Benzylaldehyde Yes No

Bourgenal No Yes

Cinnamic aldehyde Yes Yes

Citronelyl Oxyacetaldehyde No No

Cymal Yes No

Decyl aldehyde Yes No

Floral Super Yes Yes

Florhydral Yes Yes

Floralozone No No

Helional Yes No

Hydroxycitronellal No No

Laurie aldehyde Yes No

Ligustral Yes No

Lyral Yes No

Melonal Yes No

Methyl nonyl acetaldehyde No No o-anisaldehyde Yes Yes p-anisaldehyde Yes No

Pino acetaldehyde Yes Yes

P.T. Bucinal Yes No

Thiophene Carboxaldehyde Yes No

Trans-4-decenal Yes Yes

Trans Trans 2,4-Nonadienal Yes No

Undecyl aldehyde Yes No Table 9 shows the percent reduction of butylamine and butaniethiol at 40 seconds and 30 minutes, respectively, for Accords A, B, and C.

Table 9

Figure imgf000044_0001
Sensory Test - effect of volatile aldehydes on a sulfur-based malodor

Place Presto™ skillet into fume hood and turn on to 250°F. Place 80 grams of Crisco® oil into skillet and cover with skillet lid. Allow 10 minutes for equilibration. Remove skillet lid and check oil temperature with thermometer. Place 50 grams of chopped, commercially prepared garlic in water into skillet. Cover skillet with lid. Cook for 2.5 minutes or until garlic is translucent, with a portion staring to turn brown but not burn. Remove garlic from the skillet. Place 5 grams of garlic in each of 4 Petri dishes. Place covers on each Petri dish.

Place each covered Petri dish into individual test chambers. Each test chamber is 39.25 inches wide, by 25 inches deep, by 21.5 inches high with a volume of 12.2 cubic feet (0.34 cubic meters). The test chamber can be purchased from Electro-Tech Systems, Glenside, PA. Each test chamber is equipped with a fan (Newark catalog #70K9932, 115 VAC, 90CFM) purchased from Newark Electronics, Chicago, IL.

Remove the lids of the Petri dishes to expose the malodor for a dwell time sufficient to provide an initial odor intensity grade of 70-80 (about 1 minute). Once the initial odor intensity grade has been reached in a test chamber, remove the Petri dish from the test chamber.

Next, 3 Noticeables® air freshening devices, marketed by P&G, are each filled with the

Control composition shown in Table 10.

Table 10

Material Name Wt%

Benzaldehyde 0.150

Floralozone 0.097

Helional 1.455

Hydroxycitronellal 3.880

Ligustral Or Triplal 1.028

Esters 12.950

Ethers 50.190

Ketones 3.010

Lactones 0.490

Alcohols 21.610 Terpenes

The devices are set to the low intensity position and plugged into 3 of the 4 test chambers. All doors on chamber are closed.

At 5, 15, 20, 30, 45, and 60 minutes, trained evaluators open each chamber, smell the chamber for malodor intensity, and assign a malodor score, based on the scale in Table 11. The chamber door is closed but not locked between sequential evaluators. The scores are tabulated and the average score for each time interval is recorded.

Table 11

Figure imgf000045_0001

The above protocol is repeated using Prototype I shown in Table 12 (instead of Control composition) in the 3 Noticeables air freshening devices.

Table 12

Material Name Wt. %

Benzaldehyde 0.135

Floralozone 0.087

Helional 1.310

Hydroxycitronellal 3.492

Ligustral Or Triplal 0.925

o-anisaldehyde 2.500

Intreleven Aldehyde 0.500

Florhydral 1.000

Floral Super 2.500

Scentenal 1.000

Cymal 2.500

Esters 11.662

Ethers 45.171

ketones 2.705

lactones 0.437

Alcohols 19.446

Terpenes 4.632 The above protocol is repeated using Prototype 2 shown in Table 13 in the 3 Noticeables® air freshening devices.

Table 13

Figure imgf000046_0001

Fig. 3 shows that the formulation having 10% of the malodor control composition of the present invention reduces the garlic malodor more than the Control composition that lacks such malodor control composition. Sensory test - effect of volatile aldehydes on an amine -based malodor

Separate fresh ocean perch fillets from skin and add to a Magic Bullet™ food chopper. Fish meat is chopped for 35-40 seconds. 25 grams of chopped fish is weighed and fashioned into a patty suitable to fit into a 60 x 15 mm Petri dish. Repeat 3 more times so there is one fish patty in each of 4 Petri dishes. Add 40g of Crisco® oil to Presto™ skillet. Place lid on skillet and turn on to 350°F. Allow 10 minutes for equilibration. Remove lid. Cut a slit in the middle of each patty, place 1 patty into skillet, and begin frying. Replace lid. After 2.5 minutes, flip fish patty and fry an additional 2.5 minutes. Remove fish patty from skillet and blot briefly onto a paper towel for 10 seconds. Fry the remaining 3 patties in the same manner. Place each fish patty into a 60 x 15mm Petri dish and cover with a lid. Introduce each Petri dish containing a fish patty into individual test chambers. The specifications of the test chamber are the same as those in the above sulfur-based (i.e. garlic) malodor test. Remove the lids to expose the malodor for a dwell time sufficient for providing an initial odor intensity grade of 70-80 (about 1 minute). Once the initial odor intensity grade has been reached in a test chamber, remove the Petri dish from the test chamber.

Next, 3 Noticeables® air freshening devices, marketed by P&G, are each filled with the Control composition outlined in Table 10. The devices are set to the low intensity position and plugged into 3 of the 4 test chambers. All doors on chamber are closed.

At 5, 15, 20, 30, 45, and 60 minutes, trained evaluators open each chamber, smell the chamber for malodor intensity, and assign a malodor score, based on the scale in Table 9. The chamber door is closed but not locked between sequential evaluators. The scores are tabulated and the average score for each time interval is recorded.

The above protocol is repeated using Prototype I shown in Table 10 (instead of Control composition) in the 3 Noticeables® air freshening devices. The above protocol is also repeated using Prototype 2 shown in Table 11 in the 3 Noticeables® air freshening devices.

Fig. 4 shows that the formulation having 10% of the malodor control composition of the present invention reduces the fish malodor more than the Control that lacks such malodor control composition. Effect of acid catalysts on sulfur-based malodors

Malodor standards are prepared by pipeting 1 mL of butanethiol (sulfur-based malodor) into a 1.2 liter gas sampling bag. The bag is then filled to volume with nitrogen and allowed to sit for at least 12 hours to equilibrate.

A 1 μΐ aliquot of each of the following samples are pipeted into individual 10 mL silanized headspace vials in duplicate. The following samples were analyzed: Thiophene carboxyaldehyde as a control, and a 50/50 mixture of Thiophene Carboxaldehyde and each of the following acid catalysts, at 0.04%, at 0.10%, at 0.43% in DPM, at 1.02% in DPM, and at 2.04% in DPM, is pipeted into individual 10 mL silanized headspace vials: phenol, mesitylenic acid, caprylic acid, succinic acid, pivalic acid, tiglic acid, and benzoic acid. The vials are sealed and allowed to equilibrate for at least 12 hours.

After the equilibration period, 1.5 mL of the target malodor standard is injected into each vial containing a sample. The samples are held at room temperature for 30 minutes prior to injection. Samples are then analyzed using a GC/MS with a DB-5, 20 m, 1 μηι film thickness column with an MPS-2 autosampler utilizing static headspace function. A 1 mL headspace syringe is used to inject 250 μΕ of each sample into the system. As with the samples, a repetition of at least 2 of the malodor standard is run according to the respective method. Data is analyzed by ion extraction on each total ion current current (56 for thiol), and the area is used to calculate the % reduction from the malodor standard for each acid catalyst sample.

Fig. 5 demonstrates that low vapor pressure acid catalysts provide up to 3 times better reduction of sulfur-based malodors in comparison to the control.

All percentages stated herein are by weight unless otherwise specified. It should be understood that every maximum numerical limitation given throughout this specification will include 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.

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 a functionally equivalent range surrounding that value. For example, a dimension disclosed as "40 mm" is intended to mean "about 40 mm."

Every document cited herein, including any cross referenced or related patent or application, is hereby incorporated herein by reference in its entirety unless expressly excluded or otherwise limited. The citation of any document is not an admission that it is prior art with respect to any invention disclosed or claimed herein or that it alone, or in any combination with any other reference or references, teaches, suggests or discloses any such invention. Further, 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

CLAIMS What is claimed is:
1. A freshening composition for reducing malodor comprising:
an effective amount of a malodor binding polymer;
a malodor control component comprising an effective amount of a mixture of two or more volatile aldehydes for neutralizing a malodor, wherein said two or more volatile aldehydes are selected from the group consisting of 2-ethoxy benzylaldehyde, 2- isopropyl-5-methyl-2-hexenal, 5-methyl furfural, 5-methyl-thiophene-carboxaldehyde, adoxal, p-anisaldehyde, benzylaldehyde, bourgenal, cinnamic aldehyde, cymal, decyl aldehyde, floral super, florhydral, helional, lauric aldehyde, ligustral, lyral, melonal, o- anisaldehyde, pino acetaldehyde, P.T. bucinal, thiophene carboxaldehyde, trans-4- decenal, trans trans 2,4-nonadienal, undecyl aldehyde, and mixtures thereof; and
an aqueous carrier.
2. The composition of Claim 1 wherein said two or more volatile aldehydes are selected from the group consisting of 2-ethoxy benzylaldehyde, 2-isopropyl-5-methyl-2-hexenal, 5- methyl furfural, cinnamic aldehyde, floral super, florhydral, o-anisaldehyde, pino acetaldehyde, trans-4-decenal, and mixtures thereof; preferably comprise flor super and o-anisaldehyde.
3. The composition of Claim 1 wherein said two or more volatile aldehydes have a VP from 0.001 torr to 0.100 torr.
4. The composition of Claim 1 wherein said two or more volatile aldehydes comprise a mixture of volatile aldehydes selected from the group consisting of: Accord A, Accord B, Accord C, and mixtures thereof.
5. The composition of Claim 1 wherein said two or more volatile aldehydes comprise a mixture of volatile aldehydes comprising 1% to 10% of Accord A, by weight of said malodor control component.
6. The composition of Claim 1 wherein said malodor control component further comprises 0.001% to 1% of an aliphatic aldehyde by total weight of said composition.
7. The composition of Claim 1 further comprising a buffering agent selected from the group consisting of carboxylic acid, dicarboxcylic acid, N-(2-Acetamido)-2-aminoethanesulfonic acid, and mixtures thereof.
8. The composition of Claim 1 wherein further comprising maleic acid.
9. The composition of Claim 1 wherein said composition comprises a pH of 5 to 8.
10. The composition of Claim 1 wherein said composition is free of anionic surfactants.
11. The composition of Claim 1 wherein said composition comprises no more than 3% surfactant by weight of said composition.
12. The composition of Claim 1 wherein said aqueous carrier is present in an amount of 90% to 99.5%.
13. A freshening composition for reducing malodor comprising:
an effective amount of a malodor binding polymer; and
a malodor control component comprising:
at least one volatile aldehyde; and
an acid catalyst having a vapor pressur of 0.01 to 13 at 25°C.
14. The composition of Claim 13 wherein said acid catalyst has a vapor pressure of 0.01 to 2 torr at 25°C.
15. The composition of Claim 13 wherein said acid catalyst is a carboxylic acid, preferably is 5-methyl thiophene carboxylic acid.
16. The composition of Claim 13 wherein said acid catalyst is present in an amount from 0.1% to 0.4%, by weight of said malodor control component, preferably 0.4%, by weight of said malodor control component.
17. The composition of Claim 13 wherein said at least one volatile aldehyde is a mixture of two or more volatile aldehydes selected from the group consisting of 2-ethoxy benzylaldehyde, 2-isopropyl-5-methyl-2-hexenal, 5-methyl furfural, 5-methyl-thiophene-carboxaldehyde, adoxal, p-anisaldehyde, benzylaldehyde, bourgenal, cinnamic aldehyde, cymal, decyl aldehyde, floral super, florhydral, helional, lauric aldehyde, ligustral, lyral, melonal, o-anisaldehyde, pino acetaldehyde, P.T. bucinal, thiophene carboxaldehyde, trans-4-decenal, trans trans 2,4- nonadienal, undecyl aldehyde, and mixtures thereof.
18. The composition of any one of the preceding claims wherein said malodor binding polymer is a polyamine having a molecular weight of at least 150 Daltons and 15% to 80% primary amino groups
19. The composition of any one of the preceding claims wherein said malodor binding polymer is a homopolymeric polyethyleneimine having a molecular weight of 1,000 to 2,000,000 Daltons, preferably 25,000 Daltons.
20. The composition of any one of the preceding claims wherein said malodor binding polymer is present in an amount of 0.01% to 1%, preferably 0.01% to 0.07% by weight of said composition.
21. A method of reducing malodor comprising the steps of:
a. providing the freshening composition of any one of Claims 1 or 13;
b. dispersing an effective amount of said freshening composition on an inanimate surface or in the air.
PCT/US2010/060466 2009-09-18 2010-12-15 Freshening compositions comprising malodor binding polymers and malodor control components WO2011084463A1 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
US28734809P true 2009-12-17 2009-12-17
US28736909P true 2009-12-17 2009-12-17
US28738309P true 2009-12-17 2009-12-17
US61/287,383 2009-12-17
US61/287,369 2009-12-17
US61/287,348 2009-12-17
US12/885,884 2010-09-20
US12/885,884 US20110150817A1 (en) 2009-12-17 2010-09-20 Freshening compositions comprising malodor binding polymers and malodor control components
US12/904,261 2010-10-14
US12/904,261 US20110305659A1 (en) 2009-09-18 2010-10-14 Freshening compositions comprising malodor binding polymers and malodor control components

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2012544749A JP5782046B2 (en) 2009-12-17 2010-12-15 Freshening composition comprising a malodor binding polymer and malodor control component
EP10795578A EP2512527A1 (en) 2009-12-17 2010-12-15 Freshening compositions comprising malodor binding polymers and malodor control components
KR1020127015607A KR101463727B1 (en) 2009-12-17 2010-12-15 Freshening compositions comprising malodor binding polymers and malodor control components

Publications (1)

Publication Number Publication Date
WO2011084463A1 true WO2011084463A1 (en) 2011-07-14

Family

ID=44305698

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2010/060466 WO2011084463A1 (en) 2009-09-18 2010-12-15 Freshening compositions comprising malodor binding polymers and malodor control components

Country Status (4)

Country Link
EP (1) EP2512527A1 (en)
JP (1) JP5782046B2 (en)
KR (1) KR101463727B1 (en)
WO (1) WO2011084463A1 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012097034A1 (en) * 2011-01-14 2012-07-19 The Procter & Gamble Company Compositions comprising hydrophobically modified malodor control polymers
WO2013084175A1 (en) 2011-12-09 2013-06-13 Esseoquattro Spa Material for packaging fresh food of animal origin inhibiting the development of biogenic amines
JP2015520619A (en) * 2012-04-10 2015-07-23 ザ プロクター アンド ギャンブルカンパニー Malodor reducing composition
WO2015119813A1 (en) * 2014-02-04 2015-08-13 The Procter & Gamble Company Long lasting freshening compositions
JP2015526121A (en) * 2012-06-15 2015-09-10 ザ プロクター アンド ギャンブルカンパニー Malodor control composition having activated alkenes and method
WO2019089739A1 (en) * 2017-11-03 2019-05-09 The Procter & Gamble Company Apparatus and method for reducing malodor on surfaces

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150098922A1 (en) * 2013-10-04 2015-04-09 The Procter & Gamble Company Compositions comprising polyamine polymer compatible perfume materials
US20150099689A1 (en) * 2013-10-04 2015-04-09 The Procter & Gamble Company Compositions comprising hydrophobically modified polyamine polymer compatible perfume materials
KR20150070937A (en) * 2013-12-17 2015-06-25 주식회사 엘지생활건강 Fragrance composition for deodorizing in formulation comprising an amine
WO2017171110A1 (en) * 2016-03-29 2017-10-05 주식회사 엘지생활건강 Perfume composition capable of masking odor of formulation containing amine

Citations (74)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3594328A (en) 1965-08-02 1971-07-20 Ciba Ltd Process for the encapsulation of dispersible materials
US4234627A (en) 1977-02-04 1980-11-18 The Procter & Gamble Company Fabric conditioning compositions
US4514461A (en) 1981-08-10 1985-04-30 Woo Yen Kong Fragrance impregnated fabric
US4539135A (en) 1983-06-01 1985-09-03 Colgate Palmolive Co. Perfume-containing carrier for laundry compositions
US4540721A (en) 1983-03-10 1985-09-10 The Procter & Gamble Company Method of providing odor to product container
USRE32713E (en) 1980-03-17 1988-07-12 Capsule impregnated fabric
US4882220A (en) 1988-02-02 1989-11-21 Kanebo, Ltd. Fibrous structures having a durable fragrance
US4911852A (en) 1988-10-07 1990-03-27 The Procter & Gamble Company Liquid laundry detergent with curable amine functional silicone for fabric wrinkle reduction
US4941991A (en) * 1987-10-22 1990-07-17 Rajamannan A H J Composition and process for use in neutralizing malodorous gases
US4973422A (en) 1989-01-17 1990-11-27 The Procter & Gamble Company Perfume particles for use in cleaning and conditioning compositions
US5506201A (en) 1994-04-29 1996-04-09 International Flavors & Fragrances Inc. Formulation of a fat surfactant vehicle containing a fragrance
US5651976A (en) 1993-06-17 1997-07-29 The United States Of America As Represented By The Secretary Of The Navy Controlled release of active agents using inorganic tubules
US5714137A (en) 1994-08-12 1998-02-03 The Procter & Gamble Company Uncomplexed cyclodextrin solutions for odor control on inanimate surfaces
US5858959A (en) 1997-02-28 1999-01-12 Procter & Gamble Company Delivery systems comprising zeolites and a starch hydrolysate glass
US5942217A (en) 1997-06-09 1999-08-24 The Procter & Gamble Company Uncomplexed cyclodextrin compositions for odor control
US5958870A (en) 1996-04-01 1999-09-28 The Procter & Gamble Company Betaine ester compounds of active alcohols
US6024943A (en) 1996-12-23 2000-02-15 Ness; Jeremy Nicholas Particles containing absorbed liquids and methods of making them
US6042792A (en) 1997-09-18 2000-03-28 International Flavors & Fragrances Inc. Apparatus for preparing a solid phase microparticulate composition
US6048830A (en) 1996-03-22 2000-04-11 The Procter & Gamble Company Delivery system having release barrier loaded zeolite
US6051540A (en) 1998-11-05 2000-04-18 International Flavors & Fragrances Inc. Method employing drum chilling and apparatus therefor for producing fragrance-containing long lasting solid particle
US6093691A (en) 1996-08-19 2000-07-25 The Procter & Gamble Company Rinse added fabric softening compositions and method of use for the delivery of fragrance derivatives
US6096918A (en) 1998-02-13 2000-08-01 Givaudan Roure (International) Sa Aryl-acrylic acid esters
US6103678A (en) 1996-11-07 2000-08-15 The Procter & Gamble Company Compositions comprising a perfume and an amino-functional polymer
US6106875A (en) 1997-10-08 2000-08-22 Givaudan Roure (International) Sa Method of encapsulating flavors and fragrances by controlled water transport into microcapsules
US6133228A (en) 1998-05-28 2000-10-17 Firmenich Sa Slow release of fragrant compounds in perfumery using 2-benzoyl benzoates, 2-alkanoyl benzoates or α-keto esters
US6147037A (en) 1996-08-19 2000-11-14 The Procter & Gamble Company Fragrance delivery systems
US6165953A (en) 1996-12-19 2000-12-26 The Procter & Gamble Company Dryer added fabric softening compositions and method of use for the delivery of fragrance derivatives
US6200949B1 (en) 1999-12-21 2001-03-13 International Flavors And Fragrances Inc. Process for forming solid phase controllably releasable fragrance-containing consumable articles
US6245732B1 (en) 1996-03-22 2001-06-12 The Procter Gamble Co. Delivery system having release inhibitor loaded zeolite and method for making same
US6248135B1 (en) 1994-08-12 2001-06-19 The Procter & Gamble Company Composition for reducing malodor impression on inanimate surfaces
US6277796B1 (en) 1996-12-19 2001-08-21 The Procter & Gamble Company Dryer-activated fabric conditioning and antistatic compositions with improved perfume longevity
US6316397B1 (en) 1997-06-27 2001-11-13 The Procter & Gamble Co. Pro-fragrance linear acetals and ketals
US6413920B1 (en) 1998-07-10 2002-07-02 Procter & Gamble Company Amine reaction compounds comprising one or more active ingredient
US6437150B1 (en) 1998-04-20 2002-08-20 Givaudan Sa Compounds having protected hydroxy groups
US6458754B1 (en) 1998-04-23 2002-10-01 The Procter & Gamble Company Encapsulated perfume particles and detergent compositions containing said particles
US6479682B1 (en) 1998-04-20 2002-11-12 Givaudan Sa Compounds having protected hydroxy groups
US20030036489A1 (en) 2001-05-04 2003-02-20 The Procter & Gamble Company Consumable composition comprising perfumed particles and article containing the same
WO2003015736A2 (en) 2001-08-16 2003-02-27 Quest International B.V. Perfume-containing composition
US6531444B1 (en) 2000-11-09 2003-03-11 Salvona, Llc Controlled delivery system for fabric care products
US6544945B1 (en) 1998-02-24 2003-04-08 The Procter & Gamble Company Cyclic pro-perfumes having modifiable fragrance raw material alcohol release rates
WO2003033635A1 (en) * 2001-10-19 2003-04-24 The Procter & Gamble Company Controlled benefit agent delivery system
US20030125222A1 (en) 2000-01-05 2003-07-03 Ekkehard Jahns Microcapsule preparations and detergents and cleaning agents containing microcapsules
US20030158344A1 (en) 2002-02-08 2003-08-21 Rodriques Klein A. Hydrophobe-amine graft copolymer
US6610646B2 (en) 2000-06-01 2003-08-26 The Procter & Gamble Company Enhanced duration fragrance delivery system having a non-distorted initial fragrance impression
US20030165692A1 (en) 2002-01-24 2003-09-04 Friedrich Koch Coagulates containing microcapsules
US20030195133A1 (en) 2002-04-10 2003-10-16 Adi Shefer Targeted controlled delivery compositions activated by changes in pH or salt concentration
US20030199422A1 (en) 2000-06-02 2003-10-23 Birkbeck Anthony Alexander Perfumes
US20030203829A1 (en) 2002-04-26 2003-10-30 Adi Shefer Multi component controlled delivery system for fabric care products
US6645479B1 (en) 1997-09-18 2003-11-11 International Flavors & Fragrances Inc. Targeted delivery of active/bioactive and perfuming compositions
US20030216488A1 (en) 2002-04-18 2003-11-20 The Procter & Gamble Company Compositions comprising a dispersant and microcapsules containing an active material
US20030215417A1 (en) 2002-04-18 2003-11-20 The Procter & Gamble Company Malodor-controlling compositions comprising odor control agents and microcapsules containing an active material
US20040058845A1 (en) 2002-09-05 2004-03-25 Metrot Veronique Sylvie Structured liquid fabric treatment compositions
US20040072719A1 (en) 2002-10-10 2004-04-15 Bennett Sydney William Encapsulated fragrance chemicals
US20040071742A1 (en) 2002-10-10 2004-04-15 Popplewell Lewis Michael Encapsulated fragrance chemicals
US20040071746A1 (en) 2002-10-10 2004-04-15 Popplewell Lewis Michael Encapsulated fragrance chemicals
US20040087477A1 (en) 2001-03-16 2004-05-06 Ness Jeremy Nicholas Perfume encapsulates
US20040087476A1 (en) 2002-11-01 2004-05-06 Dykstra Robert Richard Polymeric assisted delivery using separate addition
US20040091445A1 (en) 2002-11-01 2004-05-13 The Procter & Gamble Company Rinse-off personal care compositions comprising cationic perfume polymeric particles
US20040092425A1 (en) 2002-11-04 2004-05-13 The Procter & Gamble Company Liquid laundry detergent
US20040092414A1 (en) 2002-11-01 2004-05-13 Clapp Mannie Lee Rinse-off personal care compositions comprising anionic and/or nonionic perfume polymeric particles
US20040106536A1 (en) 2000-03-20 2004-06-03 Jean Mane Solid perfumed preparation in the form of microbeads and the use thereof
US20040110648A1 (en) 2002-11-01 2004-06-10 Jordan Glenn Thomas Perfume polymeric particles
US20040220074A1 (en) 2001-12-13 2004-11-04 Charles Fehr Compounds for a controlled release of active molecules
US20050003980A1 (en) 2003-06-27 2005-01-06 The Procter & Gamble Company Lipophilic fluid cleaning compositions capable of delivering scent
US6861402B1 (en) 1999-06-01 2005-03-01 The Procter & Gamble Company Pro-fragrances
US20050124530A1 (en) 2002-04-03 2005-06-09 Serge Creutz Fragrance compositions
US6956013B2 (en) 2001-04-10 2005-10-18 The Procter & Gamble Company Photo-activated pro-fragrances
WO2005102261A1 (en) 2004-03-26 2005-11-03 Dow Corning Corporation Controlled release compositions
US20060003913A1 (en) 2004-06-30 2006-01-05 The Procter & Gamble Company Perfumed liquid laundry detergent compositions with functionalized silicone fabric care agents
US6987084B2 (en) 2000-11-08 2006-01-17 The Procter & Gamble Co. Photo-labile pro-fragrance conjugates
US20060020459A1 (en) 2004-07-21 2006-01-26 Carter John A System and method for immigration tracking and intelligence
US20060039934A1 (en) 2002-08-14 2006-02-23 Ness Jeremy N Compositions comprising encapsulated material
US7018978B2 (en) 1998-10-23 2006-03-28 Procter & Gamble Company Fragrance pro-accords and aldehyde and ketone fragrance libraries
US7071151B2 (en) 2001-09-11 2006-07-04 Procter & Gamble Company Compositions comprising photo-labile perfume delivery

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3771088B2 (en) * 1999-07-28 2006-04-26 花王株式会社 Deodorant goods
JP2003321697A (en) * 2002-05-02 2003-11-14 Haarmann & Reimer Kk Deodorizing perfume composition
US7998403B2 (en) * 2003-05-05 2011-08-16 The Proctor & Gamble Company Method of freshening air
JP2006149892A (en) * 2004-11-30 2006-06-15 Lion Corp Composition for suppressing urine odor
DE102006011087A1 (en) * 2006-03-08 2007-09-13 Henkel Kgaa containing aminoalkyl groups excipient based on silicon
GB0611770D0 (en) * 2006-06-15 2006-07-26 Givaudan Sa Compounds

Patent Citations (82)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3594328A (en) 1965-08-02 1971-07-20 Ciba Ltd Process for the encapsulation of dispersible materials
US4234627A (en) 1977-02-04 1980-11-18 The Procter & Gamble Company Fabric conditioning compositions
USRE32713E (en) 1980-03-17 1988-07-12 Capsule impregnated fabric
US4514461A (en) 1981-08-10 1985-04-30 Woo Yen Kong Fragrance impregnated fabric
US4540721A (en) 1983-03-10 1985-09-10 The Procter & Gamble Company Method of providing odor to product container
US4539135A (en) 1983-06-01 1985-09-03 Colgate Palmolive Co. Perfume-containing carrier for laundry compositions
US4941991A (en) * 1987-10-22 1990-07-17 Rajamannan A H J Composition and process for use in neutralizing malodorous gases
US4882220A (en) 1988-02-02 1989-11-21 Kanebo, Ltd. Fibrous structures having a durable fragrance
US4917920A (en) 1988-02-02 1990-04-17 Kanebo, Ltd. Fibrous structures having a durable fragrance and a process for preparing the same
US4911852A (en) 1988-10-07 1990-03-27 The Procter & Gamble Company Liquid laundry detergent with curable amine functional silicone for fabric wrinkle reduction
US4973422A (en) 1989-01-17 1990-11-27 The Procter & Gamble Company Perfume particles for use in cleaning and conditioning compositions
US5651976A (en) 1993-06-17 1997-07-29 The United States Of America As Represented By The Secretary Of The Navy Controlled release of active agents using inorganic tubules
US5506201A (en) 1994-04-29 1996-04-09 International Flavors & Fragrances Inc. Formulation of a fat surfactant vehicle containing a fragrance
US5714137A (en) 1994-08-12 1998-02-03 The Procter & Gamble Company Uncomplexed cyclodextrin solutions for odor control on inanimate surfaces
US6248135B1 (en) 1994-08-12 2001-06-19 The Procter & Gamble Company Composition for reducing malodor impression on inanimate surfaces
US6245732B1 (en) 1996-03-22 2001-06-12 The Procter Gamble Co. Delivery system having release inhibitor loaded zeolite and method for making same
US6048830A (en) 1996-03-22 2000-04-11 The Procter & Gamble Company Delivery system having release barrier loaded zeolite
US5958870A (en) 1996-04-01 1999-09-28 The Procter & Gamble Company Betaine ester compounds of active alcohols
US6093691A (en) 1996-08-19 2000-07-25 The Procter & Gamble Company Rinse added fabric softening compositions and method of use for the delivery of fragrance derivatives
US6147037A (en) 1996-08-19 2000-11-14 The Procter & Gamble Company Fragrance delivery systems
US6103678A (en) 1996-11-07 2000-08-15 The Procter & Gamble Company Compositions comprising a perfume and an amino-functional polymer
US6277796B1 (en) 1996-12-19 2001-08-21 The Procter & Gamble Company Dryer-activated fabric conditioning and antistatic compositions with improved perfume longevity
US6165953A (en) 1996-12-19 2000-12-26 The Procter & Gamble Company Dryer added fabric softening compositions and method of use for the delivery of fragrance derivatives
US6024943A (en) 1996-12-23 2000-02-15 Ness; Jeremy Nicholas Particles containing absorbed liquids and methods of making them
US5858959A (en) 1997-02-28 1999-01-12 Procter & Gamble Company Delivery systems comprising zeolites and a starch hydrolysate glass
US5942217A (en) 1997-06-09 1999-08-24 The Procter & Gamble Company Uncomplexed cyclodextrin compositions for odor control
US6316397B1 (en) 1997-06-27 2001-11-13 The Procter & Gamble Co. Pro-fragrance linear acetals and ketals
US6042792A (en) 1997-09-18 2000-03-28 International Flavors & Fragrances Inc. Apparatus for preparing a solid phase microparticulate composition
US6645479B1 (en) 1997-09-18 2003-11-11 International Flavors & Fragrances Inc. Targeted delivery of active/bioactive and perfuming compositions
US6106875A (en) 1997-10-08 2000-08-22 Givaudan Roure (International) Sa Method of encapsulating flavors and fragrances by controlled water transport into microcapsules
US6096918A (en) 1998-02-13 2000-08-01 Givaudan Roure (International) Sa Aryl-acrylic acid esters
US6544945B1 (en) 1998-02-24 2003-04-08 The Procter & Gamble Company Cyclic pro-perfumes having modifiable fragrance raw material alcohol release rates
US6437150B1 (en) 1998-04-20 2002-08-20 Givaudan Sa Compounds having protected hydroxy groups
US6479682B1 (en) 1998-04-20 2002-11-12 Givaudan Sa Compounds having protected hydroxy groups
US6458754B1 (en) 1998-04-23 2002-10-01 The Procter & Gamble Company Encapsulated perfume particles and detergent compositions containing said particles
US6218355B1 (en) 1998-05-28 2001-04-17 Firmenich Sa Slow release of fragrant compounds in perfumery using a keto esters
US6133228A (en) 1998-05-28 2000-10-17 Firmenich Sa Slow release of fragrant compounds in perfumery using 2-benzoyl benzoates, 2-alkanoyl benzoates or α-keto esters
US6413920B1 (en) 1998-07-10 2002-07-02 Procter & Gamble Company Amine reaction compounds comprising one or more active ingredient
US7018978B2 (en) 1998-10-23 2006-03-28 Procter & Gamble Company Fragrance pro-accords and aldehyde and ketone fragrance libraries
US6051540A (en) 1998-11-05 2000-04-18 International Flavors & Fragrances Inc. Method employing drum chilling and apparatus therefor for producing fragrance-containing long lasting solid particle
US6861402B1 (en) 1999-06-01 2005-03-01 The Procter & Gamble Company Pro-fragrances
US6200949B1 (en) 1999-12-21 2001-03-13 International Flavors And Fragrances Inc. Process for forming solid phase controllably releasable fragrance-containing consumable articles
US20030125222A1 (en) 2000-01-05 2003-07-03 Ekkehard Jahns Microcapsule preparations and detergents and cleaning agents containing microcapsules
US20040106536A1 (en) 2000-03-20 2004-06-03 Jean Mane Solid perfumed preparation in the form of microbeads and the use thereof
US6610646B2 (en) 2000-06-01 2003-08-26 The Procter & Gamble Company Enhanced duration fragrance delivery system having a non-distorted initial fragrance impression
US20030199422A1 (en) 2000-06-02 2003-10-23 Birkbeck Anthony Alexander Perfumes
US7109153B2 (en) 2000-11-08 2006-09-19 Procter & Gamble Company Photo-labile pro-fragrance conjugates
US20060223726A1 (en) 2000-11-08 2006-10-05 Dykstra Robert R Photo-labile pro-fragrance conjugates
US6987084B2 (en) 2000-11-08 2006-01-17 The Procter & Gamble Co. Photo-labile pro-fragrance conjugates
US7119060B2 (en) 2000-11-09 2006-10-10 Salvona Ip, Llc Controlled delivery system for fabric care products
US6531444B1 (en) 2000-11-09 2003-03-11 Salvona, Llc Controlled delivery system for fabric care products
US20040087477A1 (en) 2001-03-16 2004-05-06 Ness Jeremy Nicholas Perfume encapsulates
US6956013B2 (en) 2001-04-10 2005-10-18 The Procter & Gamble Company Photo-activated pro-fragrances
US20030036489A1 (en) 2001-05-04 2003-02-20 The Procter & Gamble Company Consumable composition comprising perfumed particles and article containing the same
WO2003015736A2 (en) 2001-08-16 2003-02-27 Quest International B.V. Perfume-containing composition
US7071151B2 (en) 2001-09-11 2006-07-04 Procter & Gamble Company Compositions comprising photo-labile perfume delivery
US20030158079A1 (en) * 2001-10-19 2003-08-21 The Procter & Gamble Company Controlled benefit agent delivery system
WO2003033635A1 (en) * 2001-10-19 2003-04-24 The Procter & Gamble Company Controlled benefit agent delivery system
US20040220074A1 (en) 2001-12-13 2004-11-04 Charles Fehr Compounds for a controlled release of active molecules
US20030165692A1 (en) 2002-01-24 2003-09-04 Friedrich Koch Coagulates containing microcapsules
US20030158344A1 (en) 2002-02-08 2003-08-21 Rodriques Klein A. Hydrophobe-amine graft copolymer
US20050143282A1 (en) 2002-04-03 2005-06-30 Serge Creutz Emulsions
US20050124530A1 (en) 2002-04-03 2005-06-09 Serge Creutz Fragrance compositions
US20030195133A1 (en) 2002-04-10 2003-10-16 Adi Shefer Targeted controlled delivery compositions activated by changes in pH or salt concentration
US20030215417A1 (en) 2002-04-18 2003-11-20 The Procter & Gamble Company Malodor-controlling compositions comprising odor control agents and microcapsules containing an active material
US20030216488A1 (en) 2002-04-18 2003-11-20 The Procter & Gamble Company Compositions comprising a dispersant and microcapsules containing an active material
US20030203829A1 (en) 2002-04-26 2003-10-30 Adi Shefer Multi component controlled delivery system for fabric care products
US20060039934A1 (en) 2002-08-14 2006-02-23 Ness Jeremy N Compositions comprising encapsulated material
US20040058845A1 (en) 2002-09-05 2004-03-25 Metrot Veronique Sylvie Structured liquid fabric treatment compositions
US20040071742A1 (en) 2002-10-10 2004-04-15 Popplewell Lewis Michael Encapsulated fragrance chemicals
US20040072720A1 (en) 2002-10-10 2004-04-15 Joseph Brain Encapsulated fragrance chemicals
US20040071746A1 (en) 2002-10-10 2004-04-15 Popplewell Lewis Michael Encapsulated fragrance chemicals
US20040072719A1 (en) 2002-10-10 2004-04-15 Bennett Sydney William Encapsulated fragrance chemicals
US20040110648A1 (en) 2002-11-01 2004-06-10 Jordan Glenn Thomas Perfume polymeric particles
US20040087476A1 (en) 2002-11-01 2004-05-06 Dykstra Robert Richard Polymeric assisted delivery using separate addition
US20040091445A1 (en) 2002-11-01 2004-05-13 The Procter & Gamble Company Rinse-off personal care compositions comprising cationic perfume polymeric particles
US20040092414A1 (en) 2002-11-01 2004-05-13 Clapp Mannie Lee Rinse-off personal care compositions comprising anionic and/or nonionic perfume polymeric particles
US20040092425A1 (en) 2002-11-04 2004-05-13 The Procter & Gamble Company Liquid laundry detergent
US20050003980A1 (en) 2003-06-27 2005-01-06 The Procter & Gamble Company Lipophilic fluid cleaning compositions capable of delivering scent
WO2005102261A1 (en) 2004-03-26 2005-11-03 Dow Corning Corporation Controlled release compositions
US20060003913A1 (en) 2004-06-30 2006-01-05 The Procter & Gamble Company Perfumed liquid laundry detergent compositions with functionalized silicone fabric care agents
US20060020459A1 (en) 2004-07-21 2006-01-26 Carter John A System and method for immigration tracking and intelligence

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
"Perfume and Flavor Chemicals", 1969, STEFFEN ARCTANDER
A. LEO: "Comprehensive Medicinal Chemistry", vol. 4, 1990, PERGAMON PRESS, pages: 295

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012097034A1 (en) * 2011-01-14 2012-07-19 The Procter & Gamble Company Compositions comprising hydrophobically modified malodor control polymers
US9248209B2 (en) 2011-01-14 2016-02-02 The Procter & Gamble Company Compositions comprising hydrophobically modified malodor control polymers
WO2013084175A1 (en) 2011-12-09 2013-06-13 Esseoquattro Spa Material for packaging fresh food of animal origin inhibiting the development of biogenic amines
JP2015520619A (en) * 2012-04-10 2015-07-23 ザ プロクター アンド ギャンブルカンパニー Malodor reducing composition
JP2015526121A (en) * 2012-06-15 2015-09-10 ザ プロクター アンド ギャンブルカンパニー Malodor control composition having activated alkenes and method
WO2015119813A1 (en) * 2014-02-04 2015-08-13 The Procter & Gamble Company Long lasting freshening compositions
CN105980537A (en) * 2014-02-04 2016-09-28 宝洁公司 Long lasting freshening compositions
WO2019089739A1 (en) * 2017-11-03 2019-05-09 The Procter & Gamble Company Apparatus and method for reducing malodor on surfaces

Also Published As

Publication number Publication date
KR20120082952A (en) 2012-07-24
KR101463727B1 (en) 2014-11-21
EP2512527A1 (en) 2012-10-24
JP5782046B2 (en) 2015-09-24
JP2013514151A (en) 2013-04-25

Similar Documents

Publication Publication Date Title
US7135449B2 (en) Composition for removal of odors and contaminants from textiles and method
US6146621A (en) Composition for reducing malodor impression on inanimate surfaces
EP0776220B1 (en) Fabric treating composition containing beta-cyclodextrin
DE69535296T2 (en) A method for the treatment of inanimate surfaces with uncomplexed cyclodextrin solutions to odor control
JP3090951B2 (en) Composition for reducing malodor impression abiotic surface
JP3964444B2 (en) Composition for reducing malodor impression abiotic surface
US6803034B2 (en) Compositions and methods for odor and fungal control in ballistic fabric and other protective garments
US20100305021A1 (en) Perfume delivery systems for consumer goods
US6916774B2 (en) Fabric color care method
US6610648B2 (en) Malodor counteractant compositions
US5783544A (en) Composition for reducing malodor impression on inanimate surfaces
US6077318A (en) Method of using a composition for reducing malodor impression
JP3121839B2 (en) Uncomplexed cyclodextrin solutions for odor control in abiotic surface
CA2479192C (en) Malodor-controlling compositions comprising odor control agents and microcapsules containing an active material
JP4738744B2 (en) Release control method of a non-aerosol spray composition and the active substance containing microcapsule and the dispersing agent containing the active substance is a perfume
US5968404A (en) Uncomplexed cyclodextrin compositions for odor and wrinkle control
CA2330307C (en) Fabric wrinkle control composition and method
US6001343A (en) Uncomplexed cyclodextrin compositions for odor and wrinkle control
US8461089B2 (en) Dishwashing detergent composition having a malodor control component and methods of cleaning dishware
US5668097A (en) Uncomplexed cyclodextrin solutions for odor control on inanimate surfaces
US5997759A (en) Uncomplexed cyclodextrin compositions for odor control
EP0921824A1 (en) ODOR CONTROL COMPOSITIONS COMPRISING $g(b)-KETOESTER PRO-FRAGRANCES
EP1663323B1 (en) A method of spraying compositions comprising a dispersant and microcapsules containing an active material and a stabilizer
CN100376292C (en) Deodorant composition
US20030035748A1 (en) Uncomplexed cyclodextrin compositions for odor and wrinkle control

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 10795578

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase in:

Ref document number: 20127015607

Country of ref document: KR

Kind code of ref document: A

NENP Non-entry into the national phase in:

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 2012544749

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 2010795578

Country of ref document: EP