Freshening Composition

A freshening composition with C5-C8 and C9-C14 alkenals and phenolic terpenes addresses the issue of unpleasant odors and bacterial growth in interior environments by adsorbing to surfaces for balanced fragrance and antimicrobial benefits.

JP7772654B2Active Publication Date: 2025-11-18PROCTER & GAMBLE CO
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Patent Information

Application Number
JP2022080792
Authority / Receiving Office
JP · JP
Patent Type
Patents
Current Assignee / Owner
Priority Date
2021-05-30
Filing Date
2022-05-17
Publication Date
2025-11-18
Estimated Expiration
2042-05-17

AI Technical Summary

Technical Problem

Existing antibacterial cleaning compositions often have unpleasant odors due to disinfecting materials and do not provide a balanced fragrance, while conventional air fresheners fail to prevent bacterial growth on secondary odor sources in interior environments.

Method used

A freshening composition comprising C5-C8 and C9-C14 unsubstituted linear alkenals and phenolic derivatives of terpenes, free of anionic surfactants, which adsorb to permeable surfaces to provide a balanced fragrance and prevent bacterial growth.

Benefits of technology

The composition effectively freshens and prevents bacterial growth on permeable materials, reducing malodor and providing antimicrobial effects without lingering odors.

✦ Generated by Eureka AI based on patent content.

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Abstract

To provide a freshening composition for freshening an air or a surface in an indoor environment.SOLUTION: A composition contains (i) a C5-C8 unsubstituted linear alkenal, (ii) a C9-C14 unsubstituted linear alkenal, and (iii) a phenol derivative of a terpene represented by formula (I) [where R1 is an alkoxyl group or a hydroxy group, R2 is an alkyl group or hydrogen, R3 is hydrogen, R4 is hydrogen, R5 is an alkyl group or hydrogen, and R6 is hydrogen or an alkyl group, where if R5 is an alkyl group, R6 is hydrogen, or if R5 is hydrogen, R6 is an alkyl group]. The total amount of (i), (ii) and (iii) is 0.05 wt.%-20 wt.% of the composition.SELECTED DRAWING: None
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Description

[Technical Field]

[0001] FIELD OF THE INVENTION The present invention relates generally to freshening compositions and methods for freshening the air or surfaces of an interior environment. [Background technology]

[0002] In the interior environment, it is known that regular cleaning and frequent disinfection of high-touch objects and high-touch surfaces prevents bacterial growth on the objects or surfaces and prevents bacterial infection. High-touch objects and / or surfaces can be anything that is frequently touched, for example, sofas, beds, frequently used items, and kitchen and bathroom surfaces such as trash cans, toilets, wallpaper, bathtubs, and floors.

[0003] Antibacterial cleaning compositions containing materials with disinfecting or cleaning functions have been used to reduce or eliminate microorganisms, such as bacteria, present on surfaces. For example, typical disinfecting materials used in antibacterial compositions may contain, for example, peracids and / or halogen-releasing compounds, such as hypochlorite. A drawback associated with such antibacterial cleaning compositions is that the odor from such disinfecting materials may be perceived as unpleasant by consumers. While fragrances are sometimes incorporated into antibacterial cleaning compositions to mask the odor of the disinfecting materials, such compositions generally do not provide a "balanced" scent that includes high, medium, and base scent "notes." Despite the addition of fragrances, the odor from the disinfecting materials may linger or become particularly strong after cleaning.

[0004] Furthermore, toilet odors continue to emanate from the use of the toilet bowl, which is used to contain fecal waste excreted by humans, even after flushing. Fecal waste contains bacteria, which are the primary source of odors in toilets (the source that actually produces the odors). When the toilet bowl is flushed, bacterial particles spread rapidly above and around the interior area of ​​the toilet and tend to settle on various surfaces within the toilet (including, but not limited to, permeable materials such as terry towels, vinyl floor mats, and wallpaper). Such surfaces containing bacterial particles become secondary sources of odors. The use of conventional air fresheners to spray fragrances in the immediate area of ​​the toilet has been quite effective in masking the odors resulting from the primary odor sources described above. Furthermore, toilet bowl cleaner dispensers have been developed to clean and freshen toilet bowls after use. One type of dispenser for spraying cleaning and / or deodorizing chemicals onto the interior surfaces of a toilet bowl is described in U.S. Patent No. 7,603,726(B2) (Assigned to SC Johnson & Son, Inc.) However, as described in U.S. Patent No. 7,603,726(B2), while the dispenser functions by incorporating active substances into the toilet water to create a cleaning environment within the toilet bowl, it does not necessarily help prevent bacterial growth in secondary sources of malodor outside the toilet bowl. [Prior art documents] [Patent documents]

[0005] [Patent Document 1] U.S. Patent No. 7,603,726(B2) Summary of the Invention [Problem to be solved by the invention]

[0006] Therefore, there is a need to provide a freshening composition that can be used to freshen the air or surfaces in an interior environment and that provides a balanced fragrance while preventing bacterial growth on surfaces in the interior environment (thereby preventing bacterial malodor). [Means for solving the problem]

[0007] The present invention provides a freshening composition for freshening the air or surfaces of an interior environment, comprising: (i) a C5-C8 unsubstituted linear alkenal; (ii) C9-C14 unsubstituted linear alkenal; (iii) Formula (I),

[0008] [ka] [In the formula, R1 is an alkoxyl group or a hydroxyl group; R2 is an alkyl group or hydrogen; R3 is hydrogen; R4 is hydrogen; R5 is an alkyl group or hydrogen; R6 is hydrogen or an alkyl group; and phenolic derivatives of terpenes according to the formula: when R5 is an alkyl group, R6 is hydrogen, and when R5 is hydrogen, R6 is an alkyl group; the total amount of (i), (ii), and (iii) is 0.05% to 20% by weight of the composition; The present invention relates to a freshening composition, wherein the composition is substantially free of anionic surfactants. DETAILED DESCRIPTION OF THE INVENTION

[0009] The present invention relates to freshening compositions for freshening the air or surfaces in an interior environment and providing a balanced fragrance while preventing bacterial growth on surfaces in the interior environment (thereby preventing bacterial malodor).

[0010] It has been found that cleaning compositions and materials constituting and / or contained within enclosed spaces play an important role in the presence of odors in the air. Specifically, malodor-containing compounds in cleaning compositions, such as bacteria, amines, thiols, and odorous antimicrobial active agents, are often absorbed by certain substances, such as permeable materials, and re-evolatilized into the air, causing lingering malodors during periods when malodors are not otherwise being produced. It has also been surprisingly found that a freshening composition substantially free of anionic surfactants and comprising a C5-C8 unsubstituted linear alkenal, a C9-C14 unsubstituted linear alkenal, and a phenolic derivative of a terpene, when formulated at a concentration of 0.05% to 20% by weight in a freshening composition according to the present invention, can be applied to surfaces, including permeable materials, where the freshening composition continuously evaporates under passive airflow conditions to deposit the malodor-containing compounds thereon. The adhesive mixture of C5-C8 unsubstituted linear alkenals, C9-C14 unsubstituted linear alkenals, and phenolic derivatives of terpenes can adsorb to surfaces bearing permeable materials to freshen the surfaces and help prevent bacterial growth on the permeable materials.

[0011] The phenolic derivatives of terpenes are represented by the formula (I):

[0012] [ka] [In the formula, R1 is an alkoxyl group or a hydroxyl group; R2 is an alkyl group or hydrogen; R3 is hydrogen; R4 is hydrogen; R5 is an alkyl group or hydrogen; R6 is hydrogen or an alkyl group; When R5 is an alkyl group, R6 is hydrogen, and when R5 is hydrogen, R6 is an alkyl group.

[0013] By providing a mixture of a phenolic derivative of terpene and two different types of alkenals in an amount of 0.05% to 20% by weight of the freshening composition, it is possible to deliver the desired fragrance notes while providing the benefit of antimicrobial effects on surfaces in the interior environment, thereby freshening the air in the interior environment.

[0014] Providing the mixture in a freshening composition to provide the benefit of secondary antibacterial effect is advantageous because the mixture is compatible with other perfume raw materials that are generally used to provide comfort effects. Specifically, the phenolic derivative of terpene according to formula (I) is compatible with two different types of alkenals, and can achieve the dual effects of providing bacterial growth prevention effect on target surfaces while reducing malodor on the target surfaces, thereby freshening the surfaces and / or air of the interior environment. The interior environment may include a surface having a permeable material selected from the group consisting of fabric, drywall, woven fabric, paper, natural polymers, synthetic polymers, and inorganic materials, and mixtures thereof; preferably, the permeable material is selected from the group consisting of terry towel, cotton, vinyl, and combinations thereof.

[0015] In the following description, the products described are consumer products, such as toilet deodorizers, that vaporize a freshening composition in an interior bathroom occupancy, including a toilet, to provide various benefits, such as preventing bacterial growth, freshening, eliminating malodors, or fragrance the air in the bathroom. However, it is contemplated that the products may be configured for use in a variety of applications to deliver the freshening composition to benefit interior environments, such as rooms or household storage furniture in homes and commercial establishments, and air freshening products may include, but are not limited to, consumer products such as air fresheners, air fresheners, and fabric freshening products.

[0016] The product may also include a delivery member configured to contain the liquid-phase composition and evaporate the liquid-phase freshening composition therefrom. Delivery members may include porous or semi-porous substrates, including wicks, membranes, gels, and felt pads. An exemplary delivery member may be a membrane, which is a semi-permeable material that allows certain components of a substance to pass through while blocking others. For components that pass through the membrane, the membrane regulates the permeability of the component (i.e., allows certain components to pass through more quickly than others). Such components may include molecules, ions, or particles.

[0017] Prior to describing the present invention in detail, the following terms are defined for clarity of description. Terms not defined should be given their ordinary meaning as understood by one of ordinary skill in the relevant art.

[0018] An "internal environment" refers to a finite volume of space in a built environment. An internal environment can be a room in a vehicle, residential, or commercial environment, such as a sanitary facility. Sanitary facilities can include bathrooms, including bathrooms, toilets, and restrooms, and locker rooms. Internal environments can also be enclosed spaces, such as furniture for storing personal items, including, but not limited to, shoe cabinets, wardrobes, and gym lockers, as well as litter boxes, cat litter boxes, pet cages, and pet carriers. A pet carrier is a small, portable box, crate, or cage used to transport small animals, such as cats, small dogs, hamsters, and guinea pigs, from one location to another.

[0019] As used herein, "membrane" refers to a semipermeable material that allows certain components of a substance to pass through while blocking others. For components that pass through the membrane, the membrane regulates the permeability of the components (i.e., allows certain components to pass through more quickly than others). Such components can include molecules, ions, or particles.

[0020] As used herein, "microporous membrane" refers to a material that has a network of small pores.

[0021] As used herein, "natural convection" refers to the flow or movement of a liquid such as water or a gas such as air, in which the fluid motion is not generated by any external source (such as a pump, fan, suction device, etc.), but rather by portions of the fluid that are heavier than other portions.

[0022] "Non-energized" means that the product is passive and does not need to be powered by an external energy source. In particular, the product does not need to be powered by a heat source, gas, or electric current. The product may be configured as an energized device. An exemplary energized device may be an electrical device. The energized device may be an air freshener operated from an electrical outlet or a battery in an automobile, having a wick and / or membrane as described in the following description for transporting the freshening composition and / or evaporating the freshening composition therefrom, or other heating devices (e.g., a device powered by a chemical reaction such as a catalytic fuel system, a device powered by sunlight, etc.).

[0023] As used herein, "permeable material" refers to any material that allows liquids or gases to pass through, including, but not limited to, drywall, wallpaper, wood, vinyl, plastic, plaster, wallboard, fabric, upholstery, paper, woven fabrics, natural polymers, synthetic polymers, and inorganic materials, and mixtures thereof. Permeable materials may also include residues formed on inanimate surfaces, including, but not limited to, dust particles or grease on inanimate surfaces.

[0024] As used herein, "inanimate surfaces" refers to surfaces including, but not limited to, surfaces found in the home such as fabrics, carpets, floors, walls, carpet pads, towels, and the like.

[0025] As used herein, a "freshening composition" refers to a material that is volatilizable at room temperature and atmospheric pressure without the need for an additional energy source. The composition can be configured for a variety of uses, including, but not limited to, air freshening, deodorization, odor removal, malodor neutralization, pest control, insecticide, insect repellent, medication / medicine, disinfectant, sanitizer, mood enhancer, aromatherapy aid, scented composition, unscented composition, or any other use requiring a freshening composition that acts to condition, modify, or otherwise alter the air or environment of a location. Furthermore, not all of the component materials of the composition need be volatile. Any suitable composition can be used in any amount or in any form, including liquid, solid, gel, or emulsion. Materials suitable for use herein may also include non-volatile compounds, such as carrier substances (e.g., water, solvents, etc.). It should also be understood that when a composition is described herein as being "delivered," "emitted," or "released," this refers to the evaporation of volatile components of the composition, and not necessarily the emanating of non-volatile components of the composition.

[0026] Freshening Composition The freshening composition according to the present invention is substantially free of anionic surfactants and contains from 0.05% to 20% by weight of the composition of the following ingredients: (i) a C5-C8 unsubstituted linear alkenal; (ii) C9-C14 unsubstituted linear alkenal; (iii) Formula (I),

[0027] [ka] [In the formula, R1 is an alkoxyl group or a hydroxyl group; R2 is an alkyl group or hydrogen; R3 is hydrogen; R4 is hydrogen; R5 is an alkyl group or hydrogen; R6 is hydrogen or an alkyl group; When R5 is an alkyl group, R6 is hydrogen, and when R5 is hydrogen, R6 is an alkyl group.

[0028] As described above, by incorporating a mixture of C5 to C8 unsubstituted linear alkenal, C9 to C14 unsubstituted linear alkenal, and phenolic derivative of terpene within the above ranges into the composition of the present invention, the mixture is released from the composition, and the C5 to C8 unsubstituted linear alkenal, C9 to C14 unsubstituted linear alkenal, and phenolic derivative of terpene are attached to a surface including a permeable material to which bacteria are attached, thereby making it possible to freshen the surface, prevent bacterial growth on the permeable material, and reduce the bad odor caused by bacteria in the internal environment.

[0029] Specifically, the data in Example I show that a composition of the present invention having a mixture of a C6 alkenal ((E)-2-hexen-1-al), a C10 alkenal ((E)-2-decen-1-al), and a phenolic derivative of a terpene according to formula (I) (e.g., thymol) in a total weight percent of the composition provides an antibacterial activity value of greater than 2 against Gram-positive bacteria (Staphylococcus aureus) and Gram-negative bacteria (Klebsiella pneumoniae), corresponding to a bacterial growth reduction of greater than Log2.

[0030] The phenolic derivative of terpene according to Formula I can be selected from the group consisting of thymol, carvacrol, eugenol, isoeugenol, cinnamyl alcohol, vanillin, benzyl alcohol, and mixtures thereof. The technical effect of selecting a phenolic derivative of terpene from the above group is that these compounds are perfume raw materials compatible with C5-C8 unsubstituted linear alkenals and C9-C14 unsubstituted linear alkenals, allowing for the formulation of freshening compositions that can provide a fresh scent while offering the secondary benefit of preventing bacterial growth.

[0031] The freshening composition may be configured with a weight ratio of the C5-C8 unsubstituted linear alkenal and the C9-C14 unsubstituted linear alkenal to the phenolic derivative of the terpene according to formula (I) of 1:50 to 50:1, preferably 1:20 to 35:1, more preferably 1:2 to 20:1, or a combination of different weight ratios within the above ranges. The technical effect of the weight ratios is that the amounts of the C5-C8 unsubstituted linear alkenal, the C9-C14 unsubstituted linear alkenal, and the phenolic derivative of the terpene according to formula (I) can be adapted according to the volume of the internal environment, in which the freshening composition is applied so that the C5-C8 unsubstituted linear alkenal, the C9-C14 unsubstituted linear alkenal, and the phenolic derivative of the terpene according to formula (I) are present in sufficient amounts to provide freshening and antibacterial effects. For example, in one embodiment of a freshening composition for use in an interior occupancy space such as a passenger compartment of a vehicle, the freshening composition may be comprised of a C9-C14 unsubstituted linear alkenal and a phenolic derivative of a terpene according to formula (I) in a weight ratio of 2:1. In another embodiment of a freshening composition for use in an interior occupancy space such as a toilet, the freshening composition may be comprised of a C9-C14 unsubstituted linear alkenal and a phenolic derivative of a terpene according to formula (I) in a weight ratio of 7:1.

[0032] The freshening composition may be comprised of a weight ratio of C9-C14 unsubstituted linear alkenal to the phenolic derivative of terpene according to formula (I) of 1:50 to 50:1, preferably 1:20 to 30:1, more preferably 1:4 to 10:1. Without wishing to be bound by theory, a technical advantage of combining an amount of C9-C14 unsubstituted linear alkenal with the phenolic derivative of terpene according to formula (I) is that it allows for a balanced scent of the freshening composition, as the characteristic odors of the individual components do not feature prominently in the overall scent profile of the freshening composition.

[0033] The freshening composition may be comprised of an (E)-2 C9-C14 unsubstituted linear alkenal to a phenolic derivative of a terpene according to formula (I) in a weight ratio of 1:50 to 50:1, 1:20 to 20:1, 1:4 to 2:1, or a different combination of the above upper and lower weight ratio limits, or any combination of weight ratios within the above ranges.

[0034] The freshening composition may be substantially free of anionic surfactants and may comprise an (E)-2 C9 to C14 unsubstituted linear alkenal and a surfactant represented by formula (I):

[0035] [ka] [In the formula, R1 is an alkoxyl group or a hydroxyl group; R2 is an alkyl group or hydrogen; R3 is hydrogen; R4 is hydrogen; R5 is an alkyl group or hydrogen; R6 is hydrogen or an alkyl group; and a phenolic derivative of terpene according to formula (I), wherein the weight ratio of the (E)-2 C9-C14 unsubstituted linear alkenal to the phenolic derivative of terpene according to formula (I) is 1:50 to 50:1, preferably 1:20 to 20:1, and more preferably 1:4 to 2:1.

[0036] The phenolic derivative of terpene according to formula (I) may comprise a weight amount of the composition that corresponds to the amount of the (E)-2 C9-C14 unsubstituted linear alkenal, such as up to 15% by weight of the composition, 0.006% to 10% by weight, 0.01% to 7% by weight, or any combination of the above upper and lower percentage limits, or any combination of percentages within the above ranges.

[0037] The freshening composition may be composed of a weight ratio of the C5-C8 unsubstituted linear alkenal to the C9-C14 unsubstituted linear alkenal of 10:1 to 1:10, 5:1 to 1:5, 3:1 to 1:3, or a combination of different weight ratios within the above upper and lower limits, or any combination of weight ratios within the above ranges.

[0038] The C9-C14 unsubstituted straight chain alkenal may include a trans configuration, preferably an (E)-2 C9-C14 unsubstituted straight chain alkenal.

[0039] The C5-C8 unsubstituted straight chain alkenal may include a trans configuration, preferably an (E)-2 C5-C8 unsubstituted straight chain alkenal.

[0040] The C9-C14 unsubstituted linear alkenal may contain only one double bond, preferably the only double bond is at the C3, C4, or C5 position, more preferably the C2 or C3 position, even more preferably the C2 position.

[0041] The C5-C8 unsubstituted linear alkenal may contain only one double bond, preferably the only double bond is at the C2, C3, or C4 position, more preferably the C2 or C3 position, even more preferably the C2 position.

[0042] The C9-C14 unsubstituted linear alkenal may comprise 0.005% to 10% by weight, 0.01% to 8% by weight, 0.02% to 5% by weight of the composition, or a different combination of the above upper and lower percentage limits, or any combination of percentages within the above ranges. When the freshening composition is configured for use with a delivery member such as a membrane, the C9-C14 unsubstituted linear alkenal may be at a concentration of 1% to 10%, 2% to 8%, 3% to 5% by weight of the composition, or a different combination of the above upper and lower percentage limits, or any combination of percentages within the above ranges.

[0043] The C5-C8 unsubstituted linear alkenal may comprise 0.01% to 10% by weight, 0.02% to 8% by weight, 0.03% to 5% by weight of the composition, or a different combination of the above upper and lower percentage limits, or any combination of percentages within the above ranges. When the freshening composition is configured for use with a delivery member such as a membrane, the C5-C8 unsubstituted linear alkenal may be at a concentration of 1% to 10%, 2% to 8%, 3% to 5% by weight of the composition, or a different combination of the above upper and lower percentage limits, or any combination of percentages within the above ranges.

[0044] The C9 to C14 unsubstituted straight chain alkenal can be a C9 to C12, preferably a C9 to C11, more preferably a C10 unsubstituted straight chain alkenal.

[0045] The C5 to C8 unsubstituted linear alkenal may be a C5 to C7, preferably a C6 unsubstituted linear alkenal.

[0046] C9 to C14 unsubstituted linear alkenals include 2-nonen-1-al, 3-nonen-1-al, 4-nonen-1-al, 5-nonen-1-al, 2-decen-1-al, 3-decen-1-al, 4-decen-1-al, 5-decen-1-al, 2-undecen-1-al, 3-undecen-1-al, 4-undecen-1-al, 5-undecen-1-al, 2-dodecen-1-al, 3-dodecen-1-al, 4-dodecen-1-al, and 5-dodecen-1-al. and mixtures thereof, preferably selected from the group consisting of 2-nonen-1-al, 3-nonen-1-al, 4-nonen-1-al, 5-nonen-1-al, 2-decen-1-al, 3-decen-1-al, 4-decen-1-al, 5-decen-1-al, 2-tridecen-1-al, 2-tetradecen-1-al, 3-tetradecen-1-al, 4-tetradecen-1-al, 5-tetradecen-1-al, and mixtures thereof. and mixtures thereof, more preferably selected from the group consisting of 2-nonen-1-al, 3-nonen-1-al, 4-nonen-1-al, 5-nonen-1-al, 2-decen-1-al, 3-decen-1-al, 5-decen-1-al, 2-undecen-1-al, 3-undecen-1-al, 4-undecen-1-al, 5-undecen-1-al, 2-dodecen-1-al, 3-dodecen-1-al, 4-dodecen-1-al, 5-dodecen-1-al, and mixtures thereof. The aryl group may be selected from the group consisting of 2-decen-1-al, 3-decen-1-al, 4-decen-1-al, 5-decen-1-al, 2-undecen-1-al, 3-undecen-1-al, 4-undecen-1-al, 5-undecen-1-al, and mixtures thereof, and even more preferably selected from the group consisting of 2-decen-1-al, 3-decen-1-al, 4-decen-1-al, 5-decen-1-al, and mixtures thereof, and even more preferably 2-decen-1-al.

[0047] The C5 to C8 unsubstituted linear alkenal includes 2-penten-1-al, 3-penten-1-al, 4-penten-1-al, (E)-2-hexen-1-al, (Z)-2-hexen-1-al, 3-hexen-1-al, 4-hexen-1-al, 2-hepten-1-al, 3-hepten-1-al, 4-hepten-1-al, 2-octen-1-al, 3-octen-1-al, 4-octen-1-al, and mixtures thereof, preferably 2-penten-1-al, 3-penten-1-al, 4-penten-1-al, 2-hepten-1-al, 3-hepten-1-al, 4-hepten-1-al, 2-octen-1-al, 3-octen-1-al, 4-octen-1-al, and mixtures thereof. The hexen-1-al may be selected from the group consisting of (E)-2-hexen-1-al, (Z)-2-hexen-1-al, 3-hexen-1-al, 4-hexen-1-al, 2-hepten-1-al, 3-hepten-1-al, 4-hepten-1-al, and mixtures thereof, more preferably (E)-2-hexen-1-al, (Z)-2-hexen-1-al, 3-hexen-1-al, 4-hexen-1-al, and mixtures thereof, and even more preferably (E)-2-hexen-1-al.

[0048] The C5-C8 unsubstituted linear alkenal can be trans-2-hexenal, the C9-C14 unsubstituted linear alkenal can be trans-2-decenal, and the phenolic derivative of a terpene according to formula (I) can be thymol.

[0049] In the case of evaporative membrane air freshening devices, the composition can be formulated to be substantially free of water so as to sustain a continuous method for depositing the composition onto surfaces in an interior environment to provide a fresh scent, while providing antimicrobial benefits to prevent bacterial growth on the surfaces during a user's cleaning activity in the interior environment.The present invention relates to an air freshening product comprising a device having a housing with one or more openings disposed on the housing, and a container containing a freshening composition according to the present invention.

[0050] In an evaporative membrane air freshening device, the composition can be formulated to be substantially free of water to sustain a continuous method for depositing the composition onto surfaces in an interior environment to provide a fresh scent, while providing antimicrobial benefits to prevent bacterial growth on the surfaces during a user's cleaning activity in the interior environment.The present invention relates to an air freshening product comprising a device having a housing with one or more openings disposed on the housing, and a container containing a freshening composition according to the present invention.

[0051] The present invention also relates to an air freshening product operably connectable to a mounting portion for releasably attaching the device to an air vent in an interior environment, the air freshening product comprising a reservoir containing a freshening composition according to the present invention. The above-mentioned product may comprise a delivery member configured to contain the freshening composition in a liquid phase and to evaporate the liquid phase composition therefrom. The delivery member may be selected from the group consisting of a wick, a membrane, a gel, a porous or semi-porous substrate, and combinations thereof.

[0052] For instant freshening applications, such as fabric or household surface sprays, the compositions can contain at least 85% water by weight of the composition, 86% to 99.5% by weight, or any combination of the above upper and lower percentages, or any combination of percentages within the above ranges. This amount of water allows the water to evaporate quickly, minimizing residue on surfaces onto which the user sprays the composition. Freshening compositions containing at least 85% water by weight of the composition can be contained in a device, preferably selected from the group consisting of a trigger sprayer, a manual aerosol sprayer, an automatic aerosol sprayer, a fan device, and a thermal drop-on-demand device.

[0053] The following examples are intended to more fully illustrate the present invention and should not be construed as limiting thereof, as many variations thereof are possible without departing from the scope of the invention. All parts, percentages, and ratios herein are expressed as weight percent unless otherwise specified. [Example]

[0054] Sample preparation and materials 1) Inventive Compositions - Inventive compositions according to the present invention can be obtained by mixing appropriate amounts of thymol and alkenal with perfume oils to achieve the desired composition. Table 1 below lists the inventive mixtures, and Table 2 lists the inventive freshening compositions according to the present invention for different interior environments with different volumes / spaces. 2) Device - The resulting mixture can be injected into any device configuration capable of releasing the mixture. In this case, 2.6 mL of the mixture was injected into a fragrance delivery device designed for use in a car, and 6.5 mL of the mixture was injected into a fragrance delivery device designed for use in a toilet or bathroom. These devices are membrane-based and deliver fragrance continuously without electrical current. 3) Surfaces—Surfaces to which the present freshening compositions may be applied include, but are not limited to, polyurethane synthetic leather and nylon fabric, both commonly found in automobile interiors, as well as metal towels, vinyl cushions, and floor mats commonly found in toilets and bathrooms. Each surface is cut to the desired size and autoclaved. In Example II below, the synthetic leather was cut into one 5 cm x 5 cm piece, the nylon fabric into four 2 cm x 2 cm pieces, the metal towels into nine 2 cm x 2 cm pieces, the vinyl cushion into three 2 cm x 2 cm pieces, and the floor mat into one 2 cm x 2 cm piece, and the surfaces were autoclaved at 121° C. for 15 minutes at 15 psi.

[0055] [Table 1]

[0056] [Table 2] * Other ingredients include fragrance ingredients for comfort purposes only and do not contain trans-2-hexenal, trans-2-decenal, trans-4-decenal or thymol. ** Other ingredients include wetting surfactants, solvents, and odor counteractants.

[0057] Test Method I. Test Method for Deposition of Freshening Compositions on Surfaces in an Interior Environment The procedure for applying the formulation to the surface is as follows. 1) Activating the device and allowing the formulation to be released. 2) Place the device and test surface in a sealed environment. Car, toilet, and bathroom simulation: 0.35m 3 A box made of acrylic material having a volume of 3) Leave the device alone. Car simulation: The box cover is opened for 2 hours and then closed, and the fan inside the box is turned on for 1 hour each day. Total elapsed days are 6 days. Toilet and bathroom simulation: The box is always covered. Total elapsed time is 3 days. 4) A control sample (without any formulation) of each test surface is also prepared.

[0058] II. Test method for bacterial growth prevention effect Treated surfaces are tested using test methods for evaluating the antibacterial effectiveness of air freshening products developed from JIS L1902 for nylon cloth, metal cloth and floor mats, and JIS Z2801 for synthetic leather and vinyl cushions.

[0059] The Japanese Industrial Standards (JIS) L 1902 method, entitled "Test Methods for Antibacterial Properties and Antibacterial Effect of Textile Products," is a known JIS method used to test the antibacterial activity of fabrics and fibers that have been treated with antibacterial agents to prevent bacterial growth for a specified period of time. Under the JIS L 1902 method, there are three main types of tests: JIS L 1902 Bacterial liquid absorption method - Quantitative test JIS L 1902 Bacteria Transfer Method - Quantitative Test JIS L 1902 Halo Method - Qualitative Test

[0060] The JIS L 1902 bacterial liquid absorption method is used, which is detailed in one of the steps of the test method for evaluating the antibacterial effectiveness of air freshening products on nylon cloth, metal cloth, and floor mats described below.

[0061] Japanese Industrial Standards (JIS) Method Z2801, entitled "Antimicrobial Products - Testing of Antimicrobial Activity and Efficacy," is a well-known JIS method used to test the antimicrobial activity of hard surfaces, such as plastics, metals, ceramics, etc., that have been treated with an antimicrobial agent to prevent the growth of microorganisms, with the aim of preventing bacterial growth for a specified period of time.

[0062] JIS Z2801 is used in one step of the test method for evaluating the antibacterial effect of air freshening products for synthetic leather and vinyl cushions, which will be described later, and details are provided in the standard.

[0063] III. Test Methods for Evaluating the Antibacterial Efficacy of Nylon Fabric / Wiping / Floor Mat Air Freshening Products 1. Transfer 0.4 g of untreated and treated material into each 30 ml glass vial, ensuring that each glass vial contains only one permeable material. 2. The untreated and treated materials were each evaluated using the bacteria listed below according to the JIS L1902 bacterial solution absorption test method described below. Staphylococcus aureus Staphylococcus epidermidis ·Klebsiella pneumoniae Proteus mirabilis ·M Micrococcus luteus (M Micrococcus luteus) ·Escherichia coli Enterococcus hirae 3. The following steps are carried out according to JIS L 1902 bacterial liquid absorption test method. 4. Subculture each of the bacteria onto individual TSA plates overnight at 35°C for 18-24 hours to form 24-hour culture plates. 5. Take a single colony from each of the 24-hour culture plates from (4) above and suspend in 20 ml of nutrient broth in a Falcon® 50 ml tube and incubate overnight at 37°C with shaking at 120 rpm to form an overnight culture. 6. Transfer 0.2 ml of the overnight culture from (5) above into another 20 ml of nutrient broth (room temperature) in a Falcon® 50 ml tube and incubate at 37°C with shaking at 120 rpm for 3 hours to form a 3-hour culture. 7. Prepare a 5% nutrient broth solution by adding 0.5 ml of sterile nutrient broth to 9.5 ml of sterile water. 8. Using the 5% nutrient broth solution from (7) above, dilute the 3-hour culture from (6) above to approximately 1 x 10 5 An inoculum with cfu / ml is prepared. 9. Serially dilute the bacterial population in saline and plate on TSA. 10. Incubate the plate at 37°C for 24-48 hours. 11. Count the colonies on the plates to obtain the bacterial activity value at the starting time point ("Start Time"). 12. Add 0.2 ml of inoculum to each of the vials of untreated and treated material. 13. After inoculation, close the caps on each vial. 14. Incubate the vial at 37°C for 18-24 hours. For M. luteus, incubate the vial at 37°C for 48 hours. 15. To each of the above vials, add 20 ml of MLBT to neutralize the perfume actives on the material and shake on a vortex mixer for 30 seconds. 16. Serially dilute the bacterial population in saline and plate on TSA. 17. Incubate the plate at 37°C for 24-48 hours. 18. Count the colonies that appear on each TSA plate. 19. The antibacterial activity value can be calculated using the following formula. 20. Antibacterial activity value = common logarithm of the arithmetic mean of the number of bacteria obtained from untreated material after 18-24 hours of incubation - common logarithm of the number of bacteria obtained from treated material after 18-24 hours of incubation.

[0064] IV. Test Methods for Evaluating the Antibacterial Efficacy of Air Freshening Products for Synthetic Leather / Vinyl Cushions 1. Transfer 5 cm x 5 cm of untreated and treated material into separate petri dishes containing only one permeable material. 2. The untreated and treated materials were evaluated using the bacteria listed below in accordance with JIS Z2801, which will be described later. 3. Follow the steps below according to JIS Z2801. 4. Subculture each of the bacteria onto individual TSA plates overnight at 35°C for 18-24 hours to form 24-hour culture plates. 5. Pick a single colony from each of the 24-hour culture plates from (4) above, and subculture each bacterium on an individual TSA plate at 35°C overnight for 18 to 24 hours to form a 24-hour culture plate. 6. Prepare a 5% nutrient broth solution by adding 0.5 ml of sterile nutrient broth to 9.5 ml of sterile water. 7. Suspend several colonies from the second subculture plate in 5% nutrient broth solution to obtain approximately 1 x 10 5 cfu / ml. For Staphylococcus epidermidis and M luteus, dilute in tryptic soy broth. 8. Serially dilute the bacterial population in saline and plate on TSA. 9. Incubate the plate at 37°C for 24-48 hours. 10. Count the colonies on the plates to obtain the bacterial activity value at the starting time point ("Start Time"). 11. Inoculate each of the untreated and treated materials with 0.4 ml of inoculum. 12. Immediately place a 4 cm x 4 cm piece of plastic film over the inoculum and gently press it to distribute the inoculum solution underneath the film. 13. Close the cover and incubate the surface at 37°C and >90% RH for 18-24 hours. For M. luteus, incubate the surface at 37°C and >90% RH for 28 hours. 14. Add 10 ml of MLBT to each of the above Petri dishes to neutralize the fragrance actives on the materials. 15. Serially dilute the bacterial population in saline and plate on TSA. 16. Incubate the plate at 37°C for 24-48 hours. 17. Count the colonies that appear on each TSA plate. 18. The antibacterial activity value can be calculated using the following formula: 19. Antibacterial activity value = Common logarithm of the arithmetic mean of the number of bacteria obtained from untreated material after 18-24 hours of incubation - Common logarithm of the number of bacteria obtained from treated material after 18-24 hours of incubation.

[0065] V. Test Methods for Evaluating the Antimicrobial Effectiveness of Fabric Freshening Compositions 1. Subculture the following test bacteria from glycerol stock onto TSA plates (Transfer #1) and incubate at 35±2°C for 24±4 hours. Proteus mirabilis Staphylococcus epidermidis E. coli 2. Subculture the TSA plate from day 1 onto another TSA plate (Transfer #2) and incubate at 35±2°C for 24±4 hours. 3. Prepare the test inoculum by using a loop to remove colonies from the plate and make a bacterial suspension in saline. 4. Mix 9 parts of the above bacterial suspension with 1 part sterile 0.3% BSA solution. 5. Prepare three autoclaved and dried 35x35mm fabric carriers for the sample and control, and place them in sterile Petri dishes. 6. Inoculate each fabric carrier, including the control, with 50 μL of the respective inoculum. Use forceps to hold one end of the fabric carrier while the inoculum is being inoculated. Ensure the inoculum covers the entire fabric carrier before returning it to the Petri dish. 7. Dry the inoculated fabric at 35±2°C for 30 minutes. 8. Test by pipetting 1.0 ml of product onto the inoculated fabric. As a control, inoculate 1.0 ml of 0.05% (v / v) Tween 80 in 0.85% (w / v) saline per fabric carrier. 9. Allow the treated fabric carrier to dry at ambient conditions for 30 minutes. Leave the Petri dish uncovered. 10. After incubation, aseptically transfer each fabric carrier to a 50 mL tube containing 20 mL of MLBT and vortex for 30 seconds. Neutralize the fabric carriers for at least 5 minutes to prepare serial dilutions for plating. 11. Maximum of 10 for inoculum -8 , up to 10 for controls -5 , up to 10 for samples -4 Perform 10-fold serial dilutions of 10 of the inoculum -6 , 10 -7 , and 10 -8 , control 10 -3 , 10 -4 , and 10 -5 For the sample, molten TSA (approximately 48°C) was used, and the sample was diluted to 10 -4 Injection plating was performed using 1 mL twice. 12. Incubate the plates at 35±2°C for 48±2 hours. 13. The target dilution has plates containing 30-300 CFU.

[0066] result Example I - Evaporative Air Freshener - Automotive Air Freshener in a Vehicle Environment The results, set forth in Table 3 below, show that comparative composition 5, having 0.3% of a mixture of trans-2-decenal, trans-2-hexenal and thymol, has a log reduction of less than log2, i.e., significantly lower than composition 1 of the present invention.

[0067] [Table 3]

[0068] Example II - Automotive Air Freshener The results of the bacterial growth inhibitory effect of fabrics and synthetic leather treated with Composition 1 of the present invention, which has 97% perfume, 1.5% trans-2-hexenal, 0.5% trans-2-decenal, and 1% thymol by weight of the composition, are shown in Table 4 below.

[0069] [Table 4]

[0070] Example III - Toilet and Bathroom Air Freshening Composition Table 5 shows the results of the bacterial growth prevention effect measured on surfaces such as metal towels, vinyl cushions, and floor mats treated with compositions 2 and 3 of the present invention, which have 97% by weight of the composition of fragrance, 1.5% by weight of trans-2-hexenal, 0.25% by weight of trans-2-decenal, 1% by weight of trans-4-decenal, and 0.25% by weight of thymol.

[0071] [Table 5]

[0072] Example IV - Mixture for Fabric Freshening Composition Below is an example of a fabric freshening composition according to the present invention (Inventive Composition 4) that was evaluated according to Test Method V described herein. Specifically, the freshening composition comprises a perfume mixture having the ingredients shown below in Table 6. Other ingredients in the fabric freshening composition include more than 85% water and other ingredients that are well known and therefore will not be further described.

[0073] [Table 6]

[0074] In particular, the freshening composition comprises the inventive mixture of trans-2-decenal, trans-2-hexenal, and thymol in an amount of 0.13875% by weight of the composition. Inventive composition 4 has a weight ratio of trans-2-hexenal and trans-2-decenal to thymol of 12.75:15 (0.85:1), and a weight ratio of trans-2-decenal to thymol of 4.25:15 (0.28:1).

[0075] The results, shown in Table 7 below, demonstrate that a fabric freshening composition containing 0.13875% of a blend of the present invention by weight of the composition provides an antimicrobial efficacy of at least 4.

[0076] [Table 7]

[0077] An example is shown below: A. A freshening composition for freshening surfaces or air in an interior environment, comprising: (i) a C5-C8 unsubstituted linear alkenal; (ii) C9-C14 unsubstituted linear alkenal; (iii) Formula (I),

[0078] [ka] [In the formula, R1 is an alkoxyl group or a hydroxyl group; R2 is an alkyl group or hydrogen; R3 is hydrogen; R4 is hydrogen; R5 is an alkyl group or hydrogen; R6 is hydrogen or an alkyl group; and phenolic derivatives of terpenes according to the formula: when R5 is an alkyl group, R6 is hydrogen, and when R5 is hydrogen, R6 is an alkyl group; the total amount of (i), (ii), and (iii) is 0.05% to 20% by weight of the composition; A freshening composition, wherein the composition is substantially free of anionic surfactants. B. The composition according to item A, wherein the weight ratio of the C5-C8 unsubstituted linear alkenal and the C9-C14 unsubstituted linear alkenal to the phenol derivative of the terpene according to formula (I) is 1:50 to 50:1, preferably 1:20 to 35:1, more preferably 1:2 to 20:1. The composition according to item A or B, wherein the weight ratio of the C.C9-C14 unsubstituted linear alkenal to the phenol derivative of the terpene of formula (I) is 1:50-50:1, preferably 1:20-30:1, more preferably 1:4-10:1. D. (E)-2 The composition according to any one of items A to C, wherein the weight ratio of the C9 to C14 unsubstituted linear alkenal to the phenolic derivative of the terpene according to formula (I) is 1:50 to 50:1, preferably 1:20 to 20:1, more preferably 1:4 to 2:1. E. The composition according to any one of paragraphs A to D, wherein the phenolic derivative of the terpene according to formula (I) is 15% by weight or less of the composition, preferably 0.006% by weight to 10% by weight, more preferably 0.01% by weight to 7% by weight. F. The composition of any one of paragraphs A to E, wherein the phenolic derivative of a terpene according to formula (I) is selected from the group consisting of thymol, carvacrol, eugenol, isoeugenol, cinnamyl alcohol, vanillin, benzyl alcohol, and mixtures thereof. G. The composition according to any one of items A to F, wherein the weight ratio of the C5 to C8 unsubstituted linear alkenal to the C9 to C14 unsubstituted linear alkenal is 10:1 to 1:10, preferably 5:1 to 1:5, and more preferably 3:1 to 1:3. H. The composition of any one of paragraphs A to G, wherein the C9 to C14 unsubstituted linear alkenal has a trans configuration, preferably an (E)-2 C9 to C14 unsubstituted linear alkenal. I. The composition according to any one of paragraphs A to H, wherein the C5 to C8 unsubstituted linear alkenal has a trans configuration, preferably an (E)-2 C5 to C8 unsubstituted linear alkenal. J. The composition according to any one of paragraphs A to I, wherein the C9 to C14 unsubstituted linear alkenal contains only one double bond, preferably, the only double bond is at the C3, C4, or C5 position, more preferably, the C2 or C3 position, and even more preferably, the C2 position. K. The composition according to any one of paragraphs A to J, wherein the C5 to C8 unsubstituted linear alkenal contains only one double bond, preferably, the only double bond is at the C2, C3, or C4 position, more preferably at the C2 or C3 position, and even more preferably at the C2 position. L. The composition according to any one of paragraphs A to K, wherein the C9 to C14 unsubstituted linear alkenal constitutes 0.005% to 10% by weight, preferably 0.01% to 8% by weight, and even more preferably 0.02% to 5% by weight of the composition. M. The composition according to any one of paragraphs A to L, wherein the C5 to C8 unsubstituted linear alkenal constitutes 0.01% to 10% by weight, preferably 0.02% to 8% by weight, and even more preferably 0.03% to 5% by weight of the composition. N. The composition according to any one of items A to M, wherein the C9 to C14 unsubstituted linear alkenal is a C9 to C12, preferably a C9 to C11, more preferably a C10 unsubstituted linear alkenal. O. The composition according to any one of items A to N, wherein the C5 to C8 unsubstituted linear alkenal is a C5 to C7, preferably C6 unsubstituted linear alkenal. P. C9 to C14 unsubstituted linear alkenals include 2-nonen-1-al, 3-nonen-1-al, 4-nonen-1-al, 5-nonen-1-al, 2-decen-1-al, 3-decen-1-al, 4-decen-1-al, 5-decen-1-al, 2-undecen-1-al, 3-undecen-1-al, 4-undecen-1-al, 5-undecen-1-al, 2-dodecen-1-al, 3-dodecen-1-al, 4-dodecen-1-al, and 5-dodecen-1-al. and mixtures thereof, and preferably selected from the group consisting of 2-nonen-1-al, 3-nonen-1-al, 4-nonen-1-al, 5-nonen-1-al, 2-decen-1-al, 3-decen-1-al, 4-decen-1-al, 5-decen-1-al, 2-non ...5-decen-1-al, 5-decen-1-al, 5-decen-1-al, 5-decen-1-al, 5-decen-1-al, 5-decen-1-al, 5-decen-1-al, 5-decen-1-al, 5-decen-1-al, 5-decen-1-al, 5-decen-1-al, 5-decen-1-al, 5-decen-1-al, 5-decen-1- and mixtures thereof, more preferably selected from the group consisting of 2-nonen-1-al, 3-nonen-1-al, 4-nonen-1-al, 5-nonen-1-al, 2-decen-1-al, 3-decen-1-al, 4-decen-1-al, 5-undecen-1-al, 2-dodecen-1-al, 3-dodecen-1-al, 4-dodecen-1-al, 5-dodecen-1-al, and mixtures thereof, more preferably selected from the group consisting of 2-nonen-1-al, 3-nonen-1-al, 4-nonen-1-al, 5-nonen-1-al, 2-decen-1-al, 3-decen-1-al, 4-dec ... The composition according to any one of items A to O, wherein the undecen-1-al is selected from the group consisting of 2-decen-1-al, 3-decen-1-al, 4-decen-1-al, 5-decen-1-al, 2-undecen-1-al, 3-undecen-1-al, 4-undecen-1-al, 5-undecen-1-al, and mixtures thereof, and even more preferably selected from the group consisting of 2-decen-1-al, 3-decen-1-al, 4-decen-1-al, 5-decen-1-al, and mixtures thereof, and even more preferably 2-decen-1-al. Q. The C5 to C8 unsubstituted linear alkenal is 2-penten-1-al, 3-penten-1-al, 4-penten-1-al, (E)-2-hexen-1-al, (Z)-2-hexen-1-al, 3-hexen-1-al, 4-hexen-1-al, 2-hepten-1-al, 3-hepten-1-al, 4-hepten-1-al, 2-octen-1-al, 3-octen-1-al, 4-octen-1-al, and mixtures thereof, preferably 2-penten-1-al, 3-penten-1-al, 4-penten-1-al The composition according to any one of items A to P, wherein the hydroxyl group is selected from the group consisting of (E)-2-hexen-1-al, (Z)-2-hexen-1-al, 3-hexen-1-al, 4-hexen-1-al, 2-hepten-1-al, 3-hepten-1-al, 4-hepten-1-al, and mixtures thereof, more preferably (E)-2-hexen-1-al, (Z)-2-hexen-1-al, 3-hexen-1-al, 4-hexen-1-al, and mixtures thereof, and even more preferably (E)-2-hexen-1-al. R. The composition according to any one of items A to Q, wherein the C5 to C8 unsubstituted linear alkenal is trans-2-hexenal, the C9 to C14 unsubstituted linear alkenal is trans-2-decenal, and the phenol derivative of the terpene according to formula (I) is thymol. S. The composition according to any one of paragraphs A to R, wherein the composition is substantially free of water. T. The composition of any one of paragraphs A-R, wherein the composition comprises at least 85% water by weight of the composition. U. A freshening composition for freshening the air or surfaces of an interior environment, comprising: a freshening agent substantially free of anionic surfactants, and an (E)-2 C9-C14 unsubstituted linear alkenal having the formula (I):

[0079] [ka] [In the formula, R1 is an alkoxyl group or a hydroxyl group; R2 is an alkyl group or hydrogen; R3 is hydrogen; R4 is hydrogen; R5 is an alkyl group or hydrogen; R6 is hydrogen or an alkyl group; and a phenolic derivative of terpene according to formula (I), wherein the weight ratio of the (E)-2 C9-C14 unsubstituted linear alkenal to the phenolic derivative of terpene according to formula (I) is 1:50 to 50:1, preferably 1:20 to 20:1, and more preferably 1:4 to 2:1. V. The composition of any one of paragraphs A-U, wherein the interior environment comprises a surface having a permeable material selected from the group consisting of fabric, drywall, woven fabric, paper, natural polymers, synthetic polymers, and inorganic materials, and mixtures thereof, preferably the permeable material is selected from the group consisting of terry towel, cotton, vinyl, and combinations thereof. W. An air freshening product comprising a device having a housing with one or more openings disposed on the housing and a container containing the composition of any one of paragraphs A-S, U, or V, wherein the product comprises a delivery member, the delivery member configured to contain the freshening composition in a liquid phase and to allow the liquid phase composition to evaporate therefrom. X. An air freshening product operably connectable to a mounting portion for releasably attaching the device to an air vent in an interior environment, the product comprising a reservoir containing a freshening composition of any one of paragraphs A-S, U, or V, the product comprising a delivery member, the delivery member configured to contain the freshening composition in a liquid phase and to evaporate the liquid phase composition therefrom. Y. The product of paragraphs W or X, wherein the delivery member is selected from the group consisting of a wick, a membrane, a gel, a porous or semi-porous substrate, and combinations thereof.

[0080] Dimensions and values ​​disclosed herein should not be understood as being strictly limited to the exact numerical values ​​recited. Instead, unless otherwise indicated, 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."

[0081] All documents cited herein, including any cross-referenced or related patents or patent applications, and any patent applications or patents to which this application claims priority or benefit, are incorporated herein by reference in their entirety, unless expressly stated to the contrary. The citation of any document shall not be deemed to be prior art to any invention disclosed or claimed herein, or to teach, suggest, or disclose such invention, either alone or in combination with any other reference(s). Furthermore, 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.

[0082] While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.

Claims

1. 1. A freshening composition for freshening surfaces or air in an interior environment, comprising: (i) a C5-C8 unsubstituted linear alkenal; (ii) a C9-C14 unsubstituted linear alkenal; and (iii) Formula (I), 【Chemistry 1】 [In the formula, R1 is an alkoxyl group or a hydroxyl group; R2 is an alkyl group or hydrogen; R3 is hydrogen; R4 is hydrogen; R5 is an alkyl group or hydrogen; R6 is hydrogen or an alkyl group; and phenolic derivatives of terpenes according to the formula: when R5 is an alkyl group, R6 is hydrogen, and when R5 is hydrogen, R6 is an alkyl group; the total amount of (i), (ii), and (iii) is from 0.05% to 20% by weight of the composition; the composition is substantially free of anionic surfactants, the weight ratio of the C5-C8 unsubstituted linear alkenal and the C9-C14 unsubstituted linear alkenal to the phenol derivative of the terpene according to formula (I) is 1:2 to 20:1; (E)-2 The weight ratio of the C9-C14 unsubstituted linear alkenal to the phenol derivative of the terpene according to formula (I) is 1:4 to 2:1; the C5 to C8 unsubstituted linear alkenal is trans-2-hexenal, the C9 to C14 unsubstituted linear alkenal comprises trans-2-decenal, and the phenol derivative of the terpene according to formula (I) is thymol; A freshening composition, wherein the C5-C8 unsubstituted linear alkenal is 1% to 10% by weight of the composition when the freshening composition is adapted for use with a delivery member.

2. 2. The composition of claim 1, wherein the phenolic derivative of a terpene according to formula (I) is no more than 15% by weight of the composition.

3. 2. The composition of claim 1, wherein the C9-C14 unsubstituted linear alkenal comprises 0.005% to 10% by weight of the composition.

4. 2. The composition of claim 1, wherein the C5-C8 unsubstituted linear alkenal comprises 0.01% to 10% by weight of the composition.

5. The composition of claim 1 , wherein the composition is substantially free of water.

6. The composition of claim 1 , wherein the composition comprises at least 85% water by weight of the composition.

7. 1. A freshening composition for freshening the air or surfaces of an interior environment, the freshening composition being substantially free of anionic surfactants and comprising an (E)-2 C9-C14 unsubstituted linear alkenal and a compound of formula (I): 【Chemistry 2】 [In the formula, R1 is an alkoxyl group or a hydroxyl group; R2 is an alkyl group or hydrogen; R3 is hydrogen; R4 is hydrogen; R5 is an alkyl group or hydrogen; R6 is hydrogen or an alkyl group; when R5 is an alkyl group, R6 is hydrogen, and when R5 is hydrogen, R6 is an alkyl group; and a phenolic derivative of a terpene according to formula (I), wherein the weight ratio of the (E)-2 C9-C14 unsubstituted linear alkenal to the phenolic derivative of a terpene according to formula (I) is 1:4 to 2:1; the (E)-2 C9-C14 unsubstituted linear alkenal comprises trans-2-decenal, and the phenolic derivative of the terpene according to formula (I) is thymol; A freshening composition, wherein when said freshening composition is adapted for use with a delivery member, the (E)-2 C9-C14 unsubstituted linear alkenal is 0.5% to 10% by weight of said composition.

8. 10. The composition of claim 1 or 7, wherein the interior environment comprises a surface having a permeable material selected from the group consisting of fabric, drywall, woven fabric, paper, natural polymers, synthetic polymers, and inorganic materials, and mixtures thereof.

9. 10. An air freshening product comprising a device having a housing with one or more openings disposed on the housing and a container containing the composition of claim 1 or 7, wherein the product comprises a delivery member configured to contain the freshening composition in a liquid phase and to allow the composition in the liquid phase to evaporate therefrom.

10. 10. An air freshening product operably connectable to a mounting part for releasably attaching the device to an air vent in an interior environment, the product comprising a reservoir containing the freshening composition of claim 1 or 7, the product comprising a delivery member configured to contain the freshening composition in a liquid phase and to allow the composition in the liquid phase to evaporate therefrom.

11. 10. The article of manufacture of claim 9, wherein the delivery member is selected from the group consisting of a wick, a membrane, a gel, a porous or semi-porous substrate, and combinations thereof.

12. 11. The article of manufacture of claim 10, wherein the delivery member is selected from the group consisting of a wick, a membrane, a gel, a porous or semi-porous substrate, and combinations thereof.

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