Isovaleric acid odor suppressant

A specific fragrance-based isovaleric acid odor suppressant effectively reduces the odor of isovaleric acid, using compounds like γ-undecalactone and strawberry aldehyde, surpassing the efficacy of existing inhibitors.

JP7730280B2Active Publication Date: 2025-08-27S T CORP
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Patent Information

Application Number
JP2021152239
Authority / Receiving Office
JP · JP
Patent Type
Patents
Current Assignee / Owner
Filing Date
2021-09-17
Publication Date
2025-08-27
Estimated Expiration
2041-09-17

AI Technical Summary

Technical Problem

Existing fragrance ingredients do not effectively suppress the odor of isovaleric acid, and in some cases may even enhance it, making it difficult to manage body odor caused by this short-chain fatty acid.

Method used

An isovaleric acid odor suppressant containing specific fragrance compounds such as γ-undecalactone, strawberry aldehyde, ethylene brassylate, jasmal, 3-methyl-5-phenyl-1-pentanol, α-damascone, nerol, ethyl acetate, fenchol, styrallyl acetate, 4-methyl-3-decen-5-ol, rifamol, and terpineol is used to inhibit the odor.

Benefits of technology

The selected fragrance compounds provide superior odor suppression of isovaleric acid, reducing its detectability and perception, outperforming known inhibitors.

✦ Generated by Eureka AI based on patent content.

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Patent Text Reader

Abstract

To provide a novel isovaleric acid odor inhibitor or the like.SOLUTION: The present invention provides an isovaleric acid odor inhibitor or the like, containing at least one or two kinds selected from a group consisting of γ-undecalactone, strawberry aldehyde, ethylene brassylate, jasmal, 3-methyl-5-phenyl-1-pentanol, α-damascone, nerol, ethyl acetate, fenchol, styralyl acetate, 4-methyl-3-decen-5-ol, liffarome, terpineol and florhydral as an active ingredient.SELECTED DRAWING: None
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Description

[Technical Field]

[0001] The present invention relates to an agent for suppressing the odor of isovaleric acid, which contains a specific fragrance as an active ingredient. [Background technology]

[0002] Our living environment is home to a large number of malodorous molecules with different polarities and molecular weights. To eliminate these diverse malodorous molecules, various deodorizing methods have been developed. Generally, deodorizing methods are broadly divided into biological, chemical, physical, and sensory methods. Among the malodorous molecules, short-chain fatty acids, including isovaleric acid, can be deodorized chemically, i.e., by neutralization.

[0003] However, these malodorous substances often have a low threshold, making it difficult to deodorize them to a concentration that cannot be detected by chemical deodorization methods alone, and therefore sensory deodorization is often used in combination to effectively deodorize them.Sensory deodorization mainly includes (1) a method using a fragrance in excess of the malodor, known as masking deodorization, (2) a method using a fragrance with strong characteristics different from the malodor, known as pairing deodorization, (3) a method of deodorizing by using a fragrance that responds to the olfactory receptors to which malodors respond, causing adaptation, (4) a method of deodorizing by suppressing the response of the olfactory receptors to which malodors respond, and (5) a method of deodorizing by modulating or blocking signals from olfactory cells.

[0004] Isovaleric acid (3-methylbutanoic acid) is a naturally occurring short-chain fatty acid and one of the substances that cause body odor due to sweat and sebum, and has a low threshold. Several chemical deodorizers for isovaleric acid have been disclosed. For example, Patent Document 1 discloses a fragrance composition for modulating the odor of fatty acids having 2 to 6 carbon atoms, such as isovaleric acid, which contains one or more fragrances selected from hexanol, cis-3-hexenol, linalool, tetrahydrolinalool, geraniol, and ethyl 2-tert-butylcyclohexyl carbonate.

[0005] Patent Document 2 discloses 3-(3-isopropyl-phenyl)-butyraldehyde, Patent Document 3 discloses one or more compounds selected from the group consisting of 2,4,6-trimethyl-3-cyclohexene-1-carboxaldehyde, 3,5,6-trimethyl-3-cyclohexene-1-carboxaldehyde, 3-(4-tert-butylphenyl)propanal, and 3-(3-isopropyl-phenyl)-butyraldehyde, Patent Document 4 discloses 1,4-cineole or 1,8-cineole, Patent Document 5 discloses one or more compounds selected from the group consisting of 2-methylbutyric acid, 2-ethylbutyric acid, 2-ethylvaleric acid, 2-ethylhexanoic acid, 2-phenylbutyric acid, and 2-isopropylhexanoic acid, and Patent Document 6 discloses at least one compound selected from the group consisting of acetylcedrene, γ-methylionone, and galaxolide. [Prior art documents] [Patent documents]

[0006] [Patent Document 1] Japanese Patent Application Laid-Open No. 2007-31605 [Patent Document 2] Japanese Patent Application Laid-Open No. 2016-187557 [Patent Document 3] Japanese Patent Application Publication No. 2015-091802 [Patent Document 4] Japanese Patent Application Laid-Open No. 2017-113354 [Patent Document 5] Japanese Patent Application Publication No. 2018-121865 [Patent Document 6] Japanese Patent Publication No. 2020-111555 Summary of the Invention [Problem to be solved by the invention]

[0007] Therefore, an object of the present invention is to provide a novel isovaleric acid odor suppressant and the like. [Means for solving the problem]

[0008] The olfactory receptors that recognize odor molecules such as malodors are complex, and known fragrance ingredients do not necessarily suppress malodors such as the odor of isovaleric acid, and in some cases may even increase the malodor. The present inventors discovered that specific fragrance ingredients suppress the odor of isovaleric acid, leading to the completion of the present invention.

[0009] That is, the present invention provides an isovaleric acid odor inhibitor containing, as an active ingredient, one or more compounds selected from the group consisting of γ-undecalactone, strawberry aldehyde, ethylene brassylate, jasmal, 3-methyl-5-phenyl-1-pentanol, α-damascone, nerol, ethyl acetate, fenchol, styrallyl acetate, 4-methyl-3-decen-5-ol, rifaline, terpineol, and florhydral.

[0010] The present invention also provides a method for suppressing isovaleric acid odor, which comprises the step of contacting the isovaleric acid odor suppressant with isovaleric acid. [Effects of the Invention]

[0011] The isovaleric acid odor inhibitor provided by the present invention exhibits an isovaleric acid odor suppressing effect that is equal to or far superior to that of existing inhibitors. DETAILED DESCRIPTION OF THE INVENTION

[0012] The present invention uses as an active ingredient one or more selected from the group consisting of γ-undecalactone, strawberry aldehyde, ethylene brassylate, jasmal, 3-methyl-5-phenyl-1-pentanol, α-damascone, nerol, ethyl acetate, fenchol, styrallyl acetate, 4-methyl-3-decen-5-ol, rifamol, terpineol, and furhydral.

[0013] Among the above compounds, γ-undecalactone, strawberry aldehyde, ethylene brassylate, ethyl acetate, fenchol, jasmal, styrallyl acetate, α-damascone, 3-methyl-5-phenyl-1-pentanol, nerol, and 4-methyl-3-decen-5-ol are preferred. Among these, γ-undecalactone, strawberry aldehyde, ethylene brassylate, jasmal, and nerol are more preferred because they have low fragrance strength. Of these compounds, γ-undecalactone and jasmal are more preferred.

[0014] Each compound may be used alone, or two or more may be used in combination, as long as the effect of suppressing the isovaleric acid odor is not impaired. Furthermore, other fragrance components may be added to these compounds to prepare a blended fragrance. Such other fragrance components are not particularly limited as long as they do not impair the effect of suppressing the isovaleric acid odor, but examples thereof include animal fragrances such as musk, spirit cat fragrance, and dragon's laurel fragrance, abies oil, acorn oil, almond oil, angelica root oil, peper oil, bergamot oil, perch oil, bois rose oil, kayabuchi oil, gananga oil, capsicum oil, caraway oil, cardamom oil, cassia oil, celery oil, cinnamon oil, citronella oil, cognac oil, and coriaceae oil. Examples of suitable fragrances include plant-based fragrances such as under oil, cumin oil, camphor oil, basil oil, estgolan oil, eucalyptus oil, fennel oil, garlic oil, ginger oil, grapefruit oil, hop oil, lemon oil, lemongrass oil, nutmeg oil, mandarin oil, peppermint oil, orange oil, sage oil, star anise oil, turpentine oil, rosemary oil, eucalyptus oil, anise oil, lavender oil, cumin oil, cinnamon oil, and hiba oil. In addition, artificial fragrances such as synthetic fragrances or extracted fragrances can also be used as fragrances. Examples of such fragrances include hydrocarbon fragrances such as pinene and limonene, alcohol fragrances such as linalool, geraniol, citronellol, menthol, borneol, benzyl alcohol, anise alcohol, and β-phenethyl alcohol, phenol fragrances such as anethole and eugenol, aldehyde fragrances such as n-butyraldehyde, isobutyraldehyde, hexylaldehyde, citral, citronellal, benzaldehyde, and cinnamic aldehyde, ketone fragrances such as carvone, menthone, camphor, acetophenone, and ionone, lactone fragrances such as γ-butyrolactone, coumarin, and cineole, and ester fragrances such as octyl acetate, benzyl acetate, cinnamyl acetate, butyl propionate, and methyl benzoate.

[0015] The isovaleric acid odor inhibitor can be used to eliminate or neutralize the isovaleric acid odor contained in sweat, body odor, socks, etc. The isovaleric acid odor inhibitor can be applied directly to the source of the isovaleric acid odor. When the isovaleric acid odor is caused by bacterial growth, in addition to applying the isovaleric acid odor inhibitor, an antibacterial treatment to suppress bacterial growth may be performed.

[0016] The isovaleric acid odor inhibitor is expected to be incorporated into various deodorants, various air fresheners, body or face cleansers, laundry detergents, laundry softeners, cosmetics, and fragrance products. The isovaleric acid odor inhibitor is incorporated in a volatilizable state into, but not limited to, a liquid agent, a sheet-like material supported on a carrier such as fiber, a gel agent, etc.

[0017] Examples include oil-type deodorants in which an isovaleric acid odor suppressant or a blended fragrance prepared by compounding them is used as is or mixed with a suitable volatile organic solvent and then vaporized using a volatile material; water-based deodorants in which an isovaleric acid odor suppressant or a blended fragrance prepared by compounding them is solubilized in water using a surfactant or the like to form an aqueous solution, which is then vaporized using a volatile material; gel-type deodorants prepared by gelling these with a gelling agent; and deodorants in which these are absorbed into a highly water-absorbent resin.

[0018] The volatile organic solvent is not particularly limited, but examples thereof include volatile alcohols and volatile glycol ethers. Among these, volatile alcohols include lower alcohols such as methanol, ethanol, 1-propanol, and 2-propanol. Furthermore, volatile glycol ethers include ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol dimethyl ether, propylene glycol monomethyl ether, ethylene glycol monoisopropyl ether, diethylene glycol monomethyl ether, triethylene glycol monomethyl ether, propylene glycol monoethyl ether, dipropylene glycol monomethyl ether, tripropylene glycol monomethyl ether, butylene glycol monomethyl ether, 3-methoxy-1-butanol, and 3-methoxy-3-methyl-1-butanol.

[0019] The surfactant may be a nonionic surfactant, anionic surfactant, cationic surfactant, or amphoteric surfactant, either singly or in combination. The nonionic surfactant is not particularly limited, but examples thereof include polyoxyethylene alkyl ethers, polyoxyalkylene alkyl ethers, polyoxyethylene hydrogenated castor oil ethers, polyoxyethylene fatty acid esters, polyoxyethylene alkylphenyl ethers, sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters, sucrose fatty acid esters, glycerin fatty acid esters, polyoxyethylene polyoxypropylene block polymers, polyoxyethylene alkylamine ethers, fatty acid alkanolamides, tertiary amine oxides, etc. The polyoxyethylene alkyl ethers have a polyoxyethylene chain length of 3 to 18, preferably 7 to 12, and the alkyl chain may be either linear or branched, with an alkyl chain length of 8 to 22, preferably 12 to 14. Examples of the fatty acid alkanolamide include monoethanolamide and diethanolamide of coconut oil fatty acid, stearic acid, and lauric acid, and examples of the tertiary amine oxide include lauryl dimethylamine oxide, coconut oil fatty acid dimethylamine oxide, lauroylaminopropyl dimethylamine oxide, octyl dimethylamine oxide, and myristyl dimethylamine oxide.

[0020] Examples of anionic surfactants that can be used include higher fatty acid soaps, soap bases, metal soaps, N-acyl-L-glutamic acid triethanolamine, N-acyl-L-glutamic acid sodium, sodium alkyl sulfate, sodium alkyl sulfonate, polyoxyethylene alkyl ether sodium sulfate, polyoxyethylene alkyl ether phosphate, polyoxyethylene alkyl phenyl ether phosphate, coconut oil fatty acid methyl taurate sodium (N-cocoyl-N-methyl taurate sodium), triethanolamine lauryl sulfate, sodium lauryl sulfate, sodium lauroyl sarcosine, lauroyl methyl β-alanine sodium solution, and lauroyl methyl taurate sodium, and mixtures of two or more thereof can be used.

[0021] As the cationic surfactant, lanolin ethyl sulfate fatty acid aminopropylethyldimethylammonium, alkyltrimethylammonium chloride, dialkyldimethylammonium chloride, distearyldimethylammonium chloride, stearyldimethylbenzylammonium chloride, stearyltrimethylammonium chloride, benzalkonium chloride, benzethonium chloride, and the like can be used alone or in combination of two or more.

[0022] As the amphoteric surfactant, 2-alkyl-N-carboxymethyl-N-hydroxyethylimidazolinium betaine, alkyldiaminoethylglycine hydrochloride solution, lauryldimethylaminoacetic acid betaine, and the like can be used alone or in combination of two or more thereof.

[0023] Examples of gelling agents include conventionally known ones such as carrageenan, gellan gum, agar, gelatin, guar gum, pectin, locust bean gum, xanthan gum, tamarind gum, sodium alginate, isobutylene-maleic anhydride copolymer, and cellulose derivatives such as carboxymethyl cellulose.

[0024] The water-absorbing resin is not particularly limited, but examples thereof include those containing polyacrylic acid or a salt thereof, such as a crosslinked polyacrylate, partially neutralized polyacrylate, a crosslinked acrylic acid and / or a salt thereof-acrylamide copolymer, a crosslinked isobutylene-maleic anhydride copolymer, a hydrolyzate of a starch-acrylonitrile graft copolymer, a (partially) neutralized starch-acrylate copolymer, a saponified product and a partially saponified product of a vinyl acetate-acrylate copolymer, a hydrolyzate of an acrylonitrile copolymer or an acrylamide copolymer, and a modified polyvinyl alcohol.

[0025] The isovaleric acid odor suppressant may contain other components having a deodorizing effect as long as they do not impair the effect of the active ingredient, or any component used in deodorants or deodorants, depending on the purpose. Examples of such other components having a deodorizing effect include any known deodorants, such as deodorizing active ingredients extracted from various parts of plants, such as leaves, petioles, fruits, stems, roots, and bark (e.g., green tea extract); organic acids such as lactic acid, gluconic acid, succinic acid, glutaric acid, adipic acid, malic acid, tartaric acid, maleic acid, fumaric acid, itaconic acid, citric acid, benzoic acid, and salicylic acid; various amino acids and their salts; glyoxal, oxidizing agents, flavonoids, catechins, and polyphenols; porous substances such as activated carbon and zeolites; inclusion agents such as cyclodextrins; photocatalysts; and various masking agents.

[0026] Examples of optional ingredients used in deodorants and anti-odor agents include fragrances, powdered ingredients, liquid oils and fats, solid oils and fats, waxes, hydrocarbons, plant extracts, herbal ingredients, higher alcohols, lower alcohols, esters, long-chain fatty acids, surfactants (nonionic surfactants, anionic surfactants, cationic surfactants, amphoteric surfactants, etc.), sterols, polyhydric alcohols, moisturizers, water-soluble polymer compounds, thickeners, film-forming agents, bactericides, preservatives, ultraviolet absorbers, fixatives, cooling agents, warming agents, irritants, sequestering agents, sugars, amino acids, organic amines, synthetic resin emulsions, pH adjusters, antioxidants, antioxidant aids, oils, powders, capsules, chelating agents, inorganic salts, organic salt pigments, thickeners, bactericides, preservatives, antifungal agents, colorants, antifoaming agents, extenders, modulators, organic acids, polymers, polymer dispersants, enzymes, and enzyme stabilizers.

[0027] In a second embodiment, there is provided a method for inhibiting isovaleric acid odor, comprising contacting an isovaleric acid odor inhibiting agent with isovaleric acid.

[0028] Potential sources of isovaleric acid odor include clothing such as socks where bacteria that produce isovaleric acid grow, as well as livestock farms, rendering plants, starch factories, etc. However, as used in this specification, the sources to which the isovaleric acid odor inhibitor is directly applied do not include parts of the human body.

[0029] The contact can also be carried out by applying an isovaleric acid odor inhibitor to the source of isovaleric acid or the isovaleric acid odor. Application methods include sprinkling, spraying, and coating, and can be determined appropriately by those skilled in the art depending on the dosage form of the isovaleric acid odor inhibitor. It can also be combined with known isovaleric acid odor suppression methods. For example, if the isovaleric acid odor is caused by bacterial growth, an antibacterial treatment to suppress bacterial growth may be performed in addition to the application of the isovaleric acid odor inhibitor.

[0030] The timing of application is not particularly limited, and can be any time when the isovaleric acid odor is perceived. From a preventative standpoint, the isovaleric acid odor inhibitor may be applied in advance to areas where the isovaleric acid odor is expected to occur. [Example]

[0031] The present invention will be described in more detail below using examples, but the present invention is not limited to the following examples.

[0032] <Sensory test> (Test sample) The following test samples were used to test the deodorizing effect on the odor of isovaleric acid. [Table 1]

[0033] (Preparation of Masterbatch) Isovaleric acid was dissolved in dimethyl sulfoxide (DMSO) to prepare solutions (0.001 ppm, 0.01 ppm, 0.1 ppm, 1 ppm, 10 ppm, 100 ppm). Five grams of each solution was impregnated into pleated filter paper (185 mm diameter) and placed in a 500 ml beaker. The beaker was then sealed in a 10-liter bag, filled with odorless air, and left to stand at room temperature for 24 hours to prepare six types of masterbatch bags.

[0034] (Preparation of malodorous bags) The amounts of air shown in Table 2 were taken from the six types of masterbatch bags using a syringe and injected into 3-liter odor bags filled with odorless air to prepare odor bags 1 to 8. [Table 2]

[0035] (Preparation of scented bags) One gram of each of the fragrances listed in Table 1 was soaked in a pleated filter paper (90 mm diameter) and placed in a 500 ml beaker. The beaker was then sealed in a 10-liter bag, filled with odorless air, and left to stand at 25°C for 30 minutes to prepare a fragrance bag.

[0036] (Preparation of sample bags) Another set of the above malodor bags 1 to 8 was created, and 200 ml of air was taken from the above fragrance bag and injected into each of them, creating sample bags 1 to 8 in order.

[0037] (Fragrance pleasantness / unpleasantness, palatability) 200 ml of each fragrance bag was taken and filled with odorless air into a 3-liter bag. The pleasantness or unpleasantness and intensity of each fragrance were evaluated according to the following criteria. The values ​​shown are the average scores of four panelists who passed the olfactory test (T&T olfactometer method) in the Odor Judgement Examination and were confirmed to have normal sense of smell. The results are shown in Table 3.

[0038] (pleasantness / unpleasantness) -4: Extremely uncomfortable -3: Very uncomfortable -2: Unpleasant -1: Slightly uncomfortable 0: Neither pleasant nor unpleasant +1: Somewhat comfortable +2: pleasure +3: Very comfortable +4: Extremely comfortable

[0039] (strength) -3: Very weak -2: Weak -1: Slightly weak 0: Just right +1: Somewhat strong +2: Strong +3: Very strong

[0040] (Perception test of malodor caused by fragrance) The panelists were asked to smell the malodorous bags prepared above in order of increasing concentration, and those that could be determined to have the odor of isovaleric acid were marked with an ◯, and those that could not be determined to have the odor of isovaleric acid were marked with an ×. The number of the malodorous bag that could be recognized was taken as the threshold value of the odor of isovaleric acid.

[0041] Next, the panelists were asked to smell the sample bags containing the fragrance in the same order, starting with the malodor concentration. Those who could identify the odor as isovaleric acid were given a ◯, and those who could not were given an ×. The number of the malodor-recognized bag was taken as the odor threshold of isovaleric acid in the fragrance-mixed air. The value is the average of the four panelists. The results are shown in Table 3. If the threshold when the fragrance was added to a similar bag was higher than the concentration (threshold) felt when smelling the malodor alone, it was determined that the fragrance contributed to deodorization (recognition of the malodor). Specifically, a score of 2 or more higher than the threshold for the malodor alone was given a ◎, a score of 1 or more higher was given a ◯, a score of less than 1 (0 or higher) was given a △, and a score of less than 0 was given an ×. The malodor-only bag was used as a control, and its odor suppression function was not evaluated.

[0042] [Table 3]

[0043] From the above results, it can be seen that all of the fragrances Nos. 1 to 14 make the odor of isovaleric acid less noticeable. In particular, fragrances Nos. 4 to 6, 8, and 10 to 14, which had different threshold values, made the odor of isovaleric acid significantly less noticeable compared to geraniol, a known isovaleric acid odor inhibitor. Furthermore, while strong fragrances have limited uses, jasmal, strawberry aldehyde, ethylene brassylate, γ-undecalactone, and nerol, which have low strength and high odor-inhibiting effects, are particularly preferred isovaleric acid odor inhibitors and are expected to be used in a variety of applications.

Claims

1. An isovaleric acid odor suppressant containing fenchol and / or rifarom as active ingredients.

2. The isovaleric acid odor suppressant according to claim 1, further comprising, as an active ingredient, one or more selected from the group consisting of γ-undecalactone, strawberry aldehyde, ethylene brassylate, jasmal, α-damascone, nerol, ethyl acetate, styrallyl acetate, 4-methyl-3-decen-5-ol, terpineol, and furohydral.

3. 3. The isovaleric acid odor suppressant according to claim 1, wherein the active ingredient is fenchol.

4. A method for suppressing isovaleric acid odor, comprising a step of contacting the isovaleric acid odor suppressor according to any one of claims 1 to 3 with isovaleric acid.

Citation Information

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