WO2013031932A1 - p-メンタン-3,8-ジオール異性体混合物及びこれを含む冷感組成物、並びに、この冷感組成物を含む製品 - Google Patents
p-メンタン-3,8-ジオール異性体混合物及びこれを含む冷感組成物、並びに、この冷感組成物を含む製品 Download PDFInfo
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- WO2013031932A1 WO2013031932A1 PCT/JP2012/072108 JP2012072108W WO2013031932A1 WO 2013031932 A1 WO2013031932 A1 WO 2013031932A1 JP 2012072108 W JP2012072108 W JP 2012072108W WO 2013031932 A1 WO2013031932 A1 WO 2013031932A1
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- menthane
- diol
- isomer mixture
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
- A23L2/52—Adding ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
- A61K31/047—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates having two or more hydroxy groups, e.g. sorbitol
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/32—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
- A23G4/06—Chewing gum characterised by the composition containing organic or inorganic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/20—Synthetic spices, flavouring agents or condiments
- A23L27/203—Alicyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/075—Ethers or acetals
- A61K31/085—Ethers or acetals having an ether linkage to aromatic ring nuclear carbon
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/345—Alcohols containing more than one hydroxy group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
- C11B9/0034—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing six carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/24—Thermal properties
- A61K2800/244—Endothermic; Cooling; Cooling sensation
Definitions
- the present invention relates to a p-menthane-3,8-diol isomer mixture and a cooling sensation composition containing the mixture. More specifically, the present invention relates to a p-menthane-3,8-diol isomer mixture characterized in that 50% by mass or more is composed of (1S) isomer and a cooling sensation composition containing the same. Furthermore, the present invention provides a sensory stimulant composition containing the cooling sensation composition, and a fragrance composition, a food and drink, a cosmetic product, and a daily miscellaneous goods containing the cooling sensation composition or the sensory stimulant composition. , Oral compositions or pharmaceuticals.
- a refreshing sensation (cooling sensation) or a cold sensation (cooling sensation) on human skin, oral cavity, nose and throat, that is, a cooling sensation agent that gives a cooling sensation effect is a dentifrice, confectionery (eg chewing gum, candy) Etc.), cigarettes, haps, and cosmetics.
- L-Menthol L-Menthol
- L-Menthol is currently widely used as a substance that gives a refreshing feeling or cooling feeling, but its cooling effect lacks durability and has a characteristic odor and bitterness. The use concentration and the use were limited.
- an object of the present invention is to provide a p-menthane-3,8-diol isomer mixture as a cooling sensation component which does not have an unpleasant irritation, particularly bitterness, and has excellent cooling sensation strength and cooling sensation. It is providing the cooling sensation composition containing this.
- Another object of the present invention is to provide a sensory stimulant composition containing the cooling sensation composition, and a fragrance composition, food and drink, cosmetic product containing the cooling sensation composition or sensory stimulant composition, It is to provide daily miscellaneous goods, oral compositions or pharmaceutical products.
- p-menthane-3 represented by the following formula (I) is characterized in that 50% by mass or more is composed of (1S) isomers.
- 8-diol isomer mixture has been found to be excellent in cooling intensity or persistence of cooling effect and useful as a cooling component or sensory stimulant, and the present invention has been completed based on these findings. is there.
- the present invention relates to a cooling sensation composition containing a p-menthane-3,8-diol isomer mixture, in which 50% by mass or more is composed of (1S) isomer.
- the present invention also provides the cooling composition, capsaicin, gingerol, vanillyl butyl ether, vanillyl ethyl ether, vanillyl propyl ether, 4- (l-menthoxymethyl) -2-phenyl-1,3-dioxolane, 4- (1-Mentoxymethyl) -2- (3 ′, 4′-dihydroxyphenyl) -1,3-dioxolane, 4- (1-Mentoxymethyl) -2- (2′-hydroxy-3′- Methoxyphenyl) -1,3-dioxolane, 4- (1-menthoxy-methyl) -2- (4′-methoxyphenyl) -1,3-dioxolane, 4- (1-menthoxymethyl) -2- (3 ', 4'-methylenedioxyphenyl) -1,3-dioxolane, 4- (l-methoxymethyl) -2- (3'-methoxy-4'-hydroxyphenyl) -1,3 Dio
- the present invention also relates to a fragrance composition, a food / beverage product, a cosmetic product, a daily miscellaneous product, an oral composition, or a medicine containing the cooling sensation composition or the sensory stimulant composition.
- the present invention also relates to a p-menthane-3,8-diol isomer mixture in which 50% by mass or more is composed of (1S) isomer.
- the present invention provides a fragrance composition, a food / beverage product, a cosmetic product, a daily miscellaneous product, an oral composition, or a pharmaceutical comprising 0.0001 to 90% by mass of the p-menthane-3,8-diol isomer mixture. About.
- the p-menthane-3,8-diol represented by the formula (I) has no specific odor and is incorporated into various foods, oral compositions, cosmetics, daily miscellaneous goods, pharmaceuticals, etc. As a result, it is possible to impart a refreshing feeling and a cool feeling to these products, and it is possible to impart a long lasting refreshing feeling and a cool feeling. Furthermore, it exhibits excellent properties that it hardly causes an unpleasant skin irritation to the human body, and is excellent in stability without being colored during storage.
- a p-menthane-3,8-diol isomer mixture characterized in that 50% by mass or more is composed of (1S) isomer is generally widely used (1R) -p-menthane- Compared to 3,8-diol, it exhibited 2-5 times the cold feeling strength while ensuring the feature of less bitterness, and 1.5-3 times as long as the cold feeling persistence.
- (1S) isomer
- 1R p-menthane-3,8-diol isomer mixture characterized in that 50% by mass or more is composed of (1S) isomer
- (1R) -p-menthane- Compared to 3,8-diol, it exhibited 2-5 times the cold feeling strength while ensuring the feature of less bitterness, and 1.5-3 times as long as the cold feeling persistence.
- p-menthane-3,8-diol has three asymmetric carbons, and there are eight types of stereoisomers. To date, examples of the differences in cooling sensation between these isomers have been verified. Has not been reported.
- the present inventors have found that the p-menthane-3,8-diol isomer mixture characterized in that 50% by mass or more is composed of (1S) isomer as described above, Or it discovered that it was excellent in the sustainability of the cool feeling effect.
- This p-menthane-3,8-diol isomer mixture while ensuring the characteristic of less bitterness compared to (1R) -p-menthane-3,8-diol, which is widely used in general, It exhibits a cold feeling intensity of 2 to 5 times, and has a cold feeling persistence of 1.5 to 3 times.
- the p-menthane-3,8-diol isomer mixture it is more preferable that 60% by mass or more is composed of (1S) isomer, and 70% by mass or more is composed of (1S) isomer. More preferably, 80% by mass or more is more preferably composed of (1S) isomer, and 90% by mass or more is particularly preferably composed of (1S) isomer.
- this p-menthane-3,8-diol isomer mixture has a mass ratio of (1S, 3R, 4S) :( 1R, 3S, 4R) to 50:50 to 99.5: 0.5.
- 0.5 Preferably there is.
- the mass ratio of (1S, 3R, 4S) body is less than 50 in the mass ratio of (1S, 3R, 4S) body: (1R, 3S, 4R) body, high cooling sensation strength as described above. This is because an effect that the bitterness is low cannot be obtained, and if it exceeds 99.5, a manufacturing process for increasing the optical purity is required, and the manufacturing process may be complicated.
- the p-menthane-3,8-diol isomer mixture has a mass ratio of (1S, 3R, 4S) :( 1R, 3S, 4R) to 60:40 to 99.5: 0.5. More preferably, the mass ratio is more preferably 70:30 to 99.5: 0.5, and the mass ratio is more preferably 80:20 to 99.5: 0.5, The mass ratio is particularly preferably 90:10 to 99.5: 0.5.
- the p-menthane-3,8-diol isomer mixture of the present invention comprises (1S, 3R, 4S) isomer and (1S, 3S, 4S) is preferably composed of a body.
- (1S) isomers of p-menthane-3,8-diol, (1S, 3R, 4S) and (1S, 3S, 4S) isomers p-menthane-3 , 8-diol isomer mixture is relatively easy to produce, so that the production process can be simplified, and more than 90% by mass of the total composition is composed of (1S, 3R, 4S) and ( This is because the p-menthane-3,8-diol isomer mixture composed of (1S, 3S, 4S) isomers has extremely low bitterness despite extremely high cooling sensation strength.
- the method for producing the (1S) -form p-menthane-3,8-diol is not particularly limited, but for example, a method known to those skilled in the art using d-citronellal as a raw material can be employed. .
- p-menthane-3 in which 60 to 70% by mass of the total composition is composed of (1S, 3R, 4S) and 30 to 40% by mass of the total composition is composed of (1S, 3S, 4S).
- An 8-diol isomer mixture is obtained.
- the p-menthane-3,8-diol isomer mixture having such a composition can be obtained efficiently, has a particularly high cooling sensation strength and a long cooling sensation, and has a particularly low bitterness.
- a p-menthane-3,8-diol isomer mixture characterized in that 50% by mass or more in the present invention is composed of (1S) isomers alone or a cooling sensation composition or sensation as described later.
- (1S) isomers alone or a cooling sensation composition or sensation as described later.
- the present invention also relates to a cooling sensation composition containing the above-mentioned p-menthane-3,8-diol isomer mixture.
- various materials can be mixed in this cooling sensation composition depending on the purpose of use.
- the p-menthane-3,8-diol isomer mixture characterized in that 50% by mass or more of the present invention is composed of (1S) isomer, has a cooling sensation other than p-menthane-3,8-diol.
- a cooling sensation composition with enhanced cooling sensation intensity or a sensory stimulant composition described below can also be prepared.
- Cooling components other than the p-menthane-3,8-diol isomer mixture of the present invention include, for example, menthol, isopulegol, menton, camphor, pregol, cineol, mint oil, 3-menthoxypropane-1,2- Diol, N-alkyl-p-menthane-3-carboxamide, 3-menthoxy-2-methylpropane-1,2-diol, 2- (menthoxy) ethanol, 2-methyl-3- (l-menthoxy) propane-1 , 2-diol, 3-menthoxypropan-1-ol, 4-l-menthoxybutan-1-ol, menthyl 3-hydroxybutanoate, 1- (2-hydroxy-4-methylcyclohexyl) -ethanone, lactic acid Menthyl, menthol glycerin ketal, N-methyl-2,2-isopropylmethyl-3-methyl Tan'amido, menthyl glyoxylate, menthyl succinate, gluta
- cooling sensation components menthol, isopulegol, 3-menthoxypropane-1,2-diol, 2- (menthoxy) ethanol, and menthyl 3-hydroxybutanoate are preferably used. It is preferable because the effect can be freely imparted.
- the p-menthane-3,8-diol isomer mixture and the cooling component other than p-menthane-3,8-diol in the cooling composition of the present invention are in any ratio within a range not impairing the effects of the present invention.
- the ratio of p-menthane-3,8-diol and the other cooling sensation component used is preferably in the range of 1:99 to 95: 5 by mass ratio.
- the cooling sensation composition of this invention can be mix
- the present invention also relates to a sensory stimulant composition containing the cooling sensation composition described above.
- the sensory stimulant composition of the present invention means a composition that gives an effect of stimulating a sense.
- the effects of stimulating the sensation include a cooling sensation effect and a warm sensation effect. Therefore, in the present invention, the sensory stimulant composition is the above-described cooling sensation composition, and the human skin, oral cavity, nose and throat. It can also be used as a concept including a warming composition that gives a warming effect.
- a cooling solution containing this p-menthane-3,8-diol isomer mixture is used.
- a sensory stimulant composition having a cooling effect can be prepared.
- the blending amount of the p-menthane-3,8-diol isomer mixture depends on the application range of the sensory stimulant composition, for example, the type of product, the purpose of use, etc. Although it is necessary to change the application method as appropriate, it is usually preferable to use it at a concentration of 0.0001 to 20% by mass, particularly 0.001 to 5% by mass, based on the total composition of the sensory stimulant composition.
- the cooling sensation composition containing the p-menthane-3,8-diol isomer mixture of the present invention can be used as a sensory stimulant composition by using a warm sensation component in combination.
- the stimulation effect can be adjusted.
- the warming component include vanillyl ethyl ether, vanillyl propyl ether, vanillin propylene glycol acetal, ethyl vanillin propylene glycol acetal, capsaicin, gingerol, vanillyl butyl ether, 4- (l-menthoxymethyl) -2-phenyl-1 , 3-Dioxolane, 4- (1-Mentoxymethyl) -2- (3 ′, 4′-dihydroxyphenyl) -1,3-dioxolane, 4- (1-Mentoxymethyl) -2- (2′- Hydroxy-3'-methoxyphenyl) -1,3-dioxolane, 4- (1-menthoxy-methyl) -2- (4'-methoxyphen
- the content of the warm sensation component in the sensory stimulant composition may be in a range where the warm sensation effect is not imparted by the warm sensation component, usually , P-menthane-3,8-diol isomer mixture and cooling component are set to 0.001 to 0.95 times mass, preferably 0.003 to 0.5 times mass. Is done.
- the cooling sensation effect is further improved, and the cooling sensation effect is increased.
- the contents of the p-menthane-3,8-diol isomer mixture and the cooling sensation component in the sensory stimulant composition are as follows. It may be in the range where the cooling effect is not given, and is usually set to 0.001 to 0.95 times mass, preferably 0.01 to 0.5 times mass, with respect to the total mass of the warming component. Is done.
- the present invention also relates to a product containing a cooling sensation composition or sensory stimulant composition comprising the above-mentioned p-menthane-3,8-diol isomer mixture.
- the above cooling sensation composition or sensory stimulant composition may be directly blended into various products such as a fragrance composition, food and drink, cosmetics, daily miscellaneous goods, oral composition, and pharmaceuticals.
- the cooling sensation composition or sensory stimulant composition is first blended in the fragrance or fragrance composition, and the fragrance composition containing the cooling sensation composition or sensory stimulant composition (hereinafter simply referred to as “the present invention”).
- the fragrance composition according to the present invention can also be blended into a product.
- p-menthane-3,8-diol, other cooling sensation components, and warm sensation components may be added to separate fragrance compositions, and the respective fragrance compositions may be mixed into the product.
- the cooling sensation composition or sensory stimulant composition of the present invention is a cooling sensation composition or sensory stimulant composition alone or as a fragrance composition according to the present invention. It can be used to impart feeling or sensory stimulation.
- Examples of products that can be given a cooling sensation or sensory stimulation by the cooling sensation composition or sensory stimulant composition itself or the fragrance composition according to the present invention include, for example, foods and drinks, cosmetics, and daily goods. And oral compositions and pharmaceuticals.
- fragrance composition examples of the fragrance component that can be contained together with the cooling sensation composition or the sensory stimulant composition include various synthetic fragrances, natural essential oils, synthetic essential oils, citrus oils, animal fragrances, and the like.
- perfume ingredients as described in "Known and Conventional Technology Collection (Fragrance) Part I" (January 29, 1999, issued by the Patent Office) can be used.
- representative examples include ⁇ -pinene, limonene, neral, geranial, 2,5-dimethyl-4-hydroxy-3 (2H) -furanone, vanillin, ethyl vanillin, geraniol, nerol, citronellol, cis -3-hexenol, phenylethyl alcohol, styryl acetate, eugenol, rose oxide, linalool, benzaldehyde, muskone, musk T (Takasago International Corporation), Tesalon (Takasago International Corporation), and the like.
- the content of the cooling sensation composition or sensory stimulant composition in the fragrance composition according to the present invention should be adjusted according to the kind of the fragrance and other components to be prepared together, the purpose of use of the fragrance composition according to the present invention, etc. Can do.
- the content of the cooling sensation composition or sensory stimulant composition is generally 0.0001 to 90% by mass, preferably 0.001 based on the total mass of the perfume composition.
- the content is preferably -70% by mass, particularly 0.01-50% by mass. That is, the perfume composition preferably contains 0.0001 to 90% by mass, more preferably 0.01 to 50% by mass of the p-menthane-3,8-diol isomer mixture.
- the content of the cooling sensation composition or the sensory stimulant composition is preferably 0.0001 to 90% by mass with respect to the total mass of the fragrance composition. More preferably, the content is 0.01 to 50% by mass. Furthermore, the same content is preferable even when it is a daily miscellaneous goods, a composition for oral cavity, or a fragrance composition for pharmaceuticals. That is, in the perfume composition, the p-menthane-3,8-diol isomer mixture is preferably contained in an amount of 0.0001 to 90% by mass, and 0.01 to 50% by mass. Is more preferable.
- the perfume composition according to the present invention may contain one or more perfume retention agents usually used in general perfume compositions as necessary.
- perfume retention agents usually used in general perfume compositions as necessary.
- the flavor retention agent in that case include ethylene glycol, propylene glycol, dipropylene glycol, glycerin, hexyl glycol, benzyl benzoate, triethyl citrate, diethyl phthalate, hercoline, medium chain fatty acid triglyceride, medium chain fatty acid diglyceride, and the like.
- the perfume composition according to the present invention can contain one or more of these.
- Examples of the cosmetics or daily goods that can be perfumed with the cooling sensation composition or sensory stimulant composition of the present invention and the fragrance composition containing them include, for example, fragrance products, basic cosmetics, finished cosmetics, hair Cosmetics, tanning cosmetics, medicinal cosmetics, hair care products, soaps, body cleaners, bath preparations, detergents, softeners, cleaners, kitchen detergents, bleaches, aerosols, deodorants and / or fragrances, repellents, Other miscellaneous goods can be mentioned.
- -Perfume, eau de perfume, eau de toilette, eau de cologne, etc. as fragrance products;
- ⁇ As basic cosmetics, facial cream, burnishing cream, cleansing cream, cold cream, massage cream, milky lotion, lotion, beauty liquid, pack, makeup remover, etc .;
- ⁇ For finished cosmetics, foundation, powder powder, solid powder, talcum powder, lipstick, lip balm, blusher, eyeliner, mascara, eye shadow, eyebrow, eye pack, nail enamel, enamel rim bar, etc .
- medicinal cosmetics include antiperspirants, after shaving lotions and gels, permanent wave agents, medicated soaps, medicated shampoos, medicinal skin cosmetics, etc .
- -Hair care products include shampoo, rinse, rinse-in shampoo, conditioner, treatment, hair pack, etc .
- -As bath preparations bath salts (bath salts, bath tablets, bath liquids, etc.), foam baths (bubble baths, etc.), bath oils (bath perfumes, bath capsules, etc.), milk baths, bath jelly, bath cubes, etc .; -Detergents include heavy laundry detergents, light laundry detergents, liquid detergents, laundry soaps, compact detergents, powdered soaps, and the like.
- -Softeners such as softeners and furniture cares; ⁇ Cleaners, house cleaners, toilet cleaners, bathroom cleaners, glass cleaners, mold removers, drainpipe cleaners, etc .; ⁇ As kitchen detergents, kitchen soap, kitchen soap, dishwashing detergent, etc .; ⁇ As bleaching agents, oxidized bleaches (chlorine bleaches, oxygen bleaches, etc.), reduced bleaches (sulfur bleaches, etc.), optical bleaches, etc .; ⁇ As aerosols, spray type, powder spray, etc .; -As deodorant and / or fragrance, solid type, gel type, liquid type, etc .; ⁇ Repellents include emulsions, oils, wettable powders, sprays, coatings, powders, granules, capsules, sheets, etc .; Can be mentioned.
- a repellent containing a cooling sensation composition or sensory stimulant composition comprising a mixture of p-menthane-3,8-diol isomers is further N, N-diethyl-m-toluamide, 2- (2-hydroxyethyl) 1-piperidinecarboxylic acid-1-methylpropyl, 2,3,4,5-bis ( ⁇ 2-butylene) tetrahydrofurfural, 3,4-caranediol, di-n-propylisocin coronate, 3- (Nn-butyl-N-acetyl) aminopropionic acid ethyl ester di-n-butyl succinate, 2-ethyl-1,3-hexanediol, 2-hydroxyoctyl sulfide, dimethyl phthalate, (N -Carbo-sec-butoxy) -2- (2'-hydroxyethyl) piperidine and citronella oil, lemongrass oil, hyssop oil, horseradish
- compositions for oral cavity include toothpaste (toothpaste, toothpaste gel), oral cleansing agent, mouthwash, troche, chewing gum and the like.
- examples of pharmaceuticals include topical skin preparations such as haps and ointments, and oral preparations.
- cooling sensation composition or sensory stimulant composition of the present invention When the cooling sensation composition or sensory stimulant composition of the present invention and the fragrance composition containing the same are used to impart cooling sensation or sensory stimulation to various products as described above, chilling sensation or sensory stimulation is imparted.
- the cooling sensation composition or sensory stimulant composition or the The contained cooling sensation composition or perfume composition may be directly added or applied to the product as it is; the cooling sensation composition or sensory stimulant composition or the cooling sensation composition or sensory stimulant composition containing them
- the fragrance composition may be added or added in the form of a liquid dissolved in a polyhydric alcohol such as alcohols, propylene glycol, glycerin, etc .; gum arabic, tragacanth Solubilized using natural gums such as, surfactants (eg, non-ionic surfactants such as glycerin fatty acid esters and sucrose fatty acid esters, anionic surfact
- compositions may be added or applied as microcapsules by treatment with an encapsulating agent.
- the composition may be included in a clathrate such as cyclodextrin to stabilize the cooling sensation composition or sensory stimulant composition or the fragrance composition containing them, and may be used with sustained release.
- the amount or amount of the cooling sensation composition or sensory stimulant composition added to or applied to various products when applying sensation or sensory stimulation depends on the type and form of the product, the sensation or sensory stimulation effect required for the product, It can be adjusted according to the action and the like.
- the addition amount or application amount of the cooling sensation composition or sensory stimulant composition is preferably 0.0001 to 90% by mass, particularly 0.01 to 20% by mass, based on the mass of the product. It is more preferable that That is, the product preferably contains 0.0001 to 90% by mass, more preferably 0.01 to 20% by mass of the p-menthane-3,8-diol isomer mixture.
- the organic layer is washed with water for liquid separation, and further the solvent is distilled off from the organic layer, and (1S) body is 99% by mass of the total composition by vacuum distillation.
- (1S, 3R, 4S) isomer accounts for 66 mass% of the total composition, and the (1S, 3S, 4S) isomer accounts for 30 mass% of the total composition
- (1S) ⁇ p 67.5 g of a menthol-menthane-3,8-diol isomer mixture was obtained.
- the (1R) form accounts for 99% by mass of the total composition (in particular, (1R, (3S, 4R) is 66% by mass of the total composition, and (1R, 3R, 4R) is 30% by mass of the total composition) (1R) -p-menthane-3,8-diol isomer mixture 65.9 g Got.
- the (1S) -p-menthane-3,8-diol isomer mixture has a cooling sensation effect approximately 3.6 times that of the (1R) -p-menthane-3,8-diol isomer mixture.
- the (1RS) -p-menthane-3,8-diol isomer mixture has a cooling effect that is about 2.3 times that of the (1R) -p-menthane-3,8-diol isomer mixture. Turned out to be.
- Example 3 Cooling composition
- Example 3 Cooling composition
- (Examination of synergistic effect with menthol) 1-Menthol and the (1S) -p-menthane-3,8-diol isomer mixture obtained in Example 1 were mixed at a mass ratio of 95: 5 to prepare a cooling sensation composition.
- 20 ppm aqueous solutions were prepared and subjected to sensory evaluation in the mouth.
- a 20 ppm aqueous solution of l-menthol alone was also subjected to sensory evaluation in the mouth.
- the evaluation was conducted by 10 expert panelists who had experienced for more than 5 years. After 10 ml of the above aqueous solution was put into the mouth for 10 seconds, it was discharged, this time was set to 0 seconds, and the strength of refreshment (exhilaration) was evaluated. The sustainability of the refreshing strength after a minute was evaluated.
- Example 4 Sensory stimulant composition
- (1S) -p-menthane-3,8-diol isomer mixture obtained in Example 1 a sensory stimulant composition containing 0.5% by mass of the warming component vanillyl butyl ether was prepared.
- 1,000 ml of an aqueous solution of 20 ppm each was prepared and subjected to sensory evaluation in the mouth.
- the (1S) -p-menthane-3,8-diol isomer mixture alone was prepared. The sensory evaluation in the mouth was also performed on the 20 ppm aqueous solution.
- the evaluation was conducted by 10 expert panelists who had experienced for more than 5 years. After 10 ml of the above aqueous solution was put into the mouth for 10 seconds, it was discharged, this time was set to 0 seconds, and the strength of refreshment (exhilaration) was evaluated. The sustainability of the refreshing strength after a minute was evaluated.
- Example 5 Composition for oral cavity (toothpaste)]
- a toothpaste was prepared according to the following formulation.
- the toothpaste prepared by the above formulation had a refreshing feeling that was cool in the oral cavity and had no bitterness. Compared to the toothpaste that did not use the (1S) -p-menthane-3,8-diol isomer mixture of the present invention, the toothpaste of the above formulation has a long lasting cold refreshing flavor, and The persistence of the fragrance was recognized.
- Example 6 Composition for oral cavity (toothpaste gel)]
- a toothpaste gel was prepared according to the following formulation.
- ⁇ Toothpaste gel prescription> (Ingredient) (Blending amount g) l-Menthol 0.30 (1S) -p-menthane-3,8-diol isomer mixture 0.01 Sodium bicarbonate 97.69 Magnesium oxide 0.50 Polyethylene glycol 0.50 Saccharin sodium 0.20 Sodium triphosphate 0.10 Peppermint type flavor (manufactured by Takasago International Corporation) 0.70 Total 100.00
- the toothpaste gel prepared according to the above formulation had a refreshing feeling that was cool in the oral cavity and had no bitterness. Compared to the toothpaste gel that did not use the (1S) -p-menthane-3,8-diol isomer mixture of the present invention, the toothpaste gel of the above formulation had a long lasting cold refreshing flavor and extended It was accompanied by the impression of the impact effect of the flavor.
- Chewing gum was prepared according to the following formulation.
- the chewing gum prepared by the above formulation had a cool and refreshing feeling and no bitterness. Compared to chewing gum that did not use the (1S) -p-menthane-3,8-diol isomer mixture of the present invention, the chewing gum of the above formulation has a long-lasting cold refreshing flavor, with an extended flavor of It was accompanied by the impression of a shocking effect.
- Example 8 Perfume composition
- a perfume composition containing a (1S) -p-menthane-3,8-diol isomer mixture was prepared by a conventional method according to the following formulation (blending amount is parts by mass).
- ⁇ Perfume composition prescription> (Ingredient) (Blending amount g) Apple base (Takasago International Corporation) 8.0 Bergamot 14.0 Ethyl acetoacetate 5.0 Methyl dihydrojasmonate 23.0 Laurinal 3.0 Revosandor (Takasago International Corporation) 4.0 Orange oil 8.0 10-Oxa-16-hexadecanolide 8.0 Phenoxanol (made by IFF) 6.0 Stylyl acetate 3.0 Tesalon (manufactured by Takasago International Corporation) 8.0 (1S) -p-menthane-3,8-diol isomer mixture 30.0
- Example 9 Cosmetic product (shampoo)
- 100 g of shampoo containing 1.0% of the fragrance composition of Example 8 was prepared. This thing had a cool feeling and maintained the cool feeling effect.
- Example 10 Sensory stimulant composition
- a sensory stimulant composition containing a (1S) -p-menthane-3,8-diol isomer mixture was prepared by a conventional method according to the following formulation (blending amount is parts by mass).
- Chewing gum was prepared according to the following formulation.
- the chewing gum prepared by the above formulation had a cool and refreshing feeling and no bitterness. Compared to the chewing gum that did not use the sensory stimulant composition containing the (1S) -p-menthane-3,8-diol isomer mixture of the present invention, the chewing gum of the above formula emphasized the refreshing feeling, and Persistence of cold feeling was observed.
- the (1S) -p-menthane-3,8-diol isomer mixture or (1RS) -p-menthane-3,8-diol isomer mixture used in the present invention is a (1R) -p-menthane-3, Compared to the 8-diol isomer mixture, it is a cooling sensation component having excellent refreshing sensation and cooling sensation while retaining the characteristics that it does not have undesirable irritation or bitterness.
- a fragrance composition, food and drink, cosmetics, daily miscellaneous goods, oral composition or pharmaceutical comprising a composition or sensory stimulant composition.
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Abstract
Description
さらに、本発明は、該冷感組成物を含有する感覚刺激剤組成物、及びこれら冷感組成物または感覚刺激剤組成物を含有する、香料組成物、飲食品、香粧品、日用雑貨品、口腔用組成物または医薬品に関する。
上記式(I)で表されるp-メンタン-3,8-ジオールについては、これまでもいくつかの合成法が報告されている。例えば、特開2000-44924号公報では、シトロネラールに濃度0.02~1.0質量%の硫酸水溶液を作用させてパラ-メンタン-3,8-ジオールを製造する方法が報告されている。
そして、本発明における50質量%以上が(1S)体で構成されることを特徴とするp-メンタン-3,8-ジオール異性体混合物を単独で、または後述するような冷感組成物或いは感覚刺激剤組成物として製品に含有させる場合、その製品の種類、使用目的などにより、その適用範囲や適用方法を適宜変える必要があるが、通常、製品の全組成に対して0.0001~90質量%、特に0.01~20質量%の濃度で用いるのが好ましい。
本発明は、上述のp-メンタン-3,8-ジオール異性体混合物を含有する冷感組成物にも関する。この冷感組成物には、p-メンタン-3,8-ジオール異性体混合物以外にも使用する目的に応じて様々なものを混合することができる。
そして、本発明の50質量%以上が(1S)体で構成されることを特徴とするp-メンタン-3,8-ジオール異性体混合物は、p-メンタン-3,8-ジオール以外の冷感成分から選ばれる少なくとも1種を併用することにより、冷感強度を高めた冷感組成物あるいは後述する感覚刺激剤組成物を調製することもできる。
本発明の冷感組成物は、香料組成物、飲食品、香粧品、日用雑貨品、口腔用組成物または医薬品に配合することができる。
本発明は、上述の冷感組成物を含有する感覚刺激剤組成物にも関する。
ここで、本発明の感覚刺激剤組成物とは、感覚を刺激する効果を与える組成物を意味する。前記感覚を刺激する効果としては冷感効果及び温感効果を含み、したがって本発明においては、感覚刺激剤組成物は上述した冷感組成物、及び、ヒトの皮膚や口腔、鼻、喉に対して温感効果を与える温感組成物をも含む概念として用いられうる。
本発明におけるp-メンタン-3,8-ジオール異性体混合物は、強く持続性のある冷感効果を有していることから、このp-メンタン-3,8-ジオール異性体混合物を含有する冷感組成物を含有させることにより、冷感効果を有する感覚刺激剤組成物を調製することができる。感覚刺激剤組成物を調整する場合において、p-メンタン-3,8-ジオール異性体混合物の配合量は、感覚刺激剤組成物の用途、例えば製品の種類、使用目的などにより、その適用範囲や適用方法を適宜変える必要があるが、通常、感覚刺激剤組成物の全組成に対して0.0001~20質量%、特に0.001~5質量%の濃度で用いるのが好ましい。
本発明は、上述のp-メンタン-3,8-ジオール異性体混合物を含む冷感組成物または感覚刺激剤組成物を含有する製品にも関する。本発明においては、上記冷感組成物または感覚刺激剤組成物を、香料組成物、飲食品、香粧品、日用雑貨品、口腔用組成物、医薬品などの各種製品に直接配合してもよいし、上記冷感組成物または感覚刺激剤組成物を香料または香料組成物中にまず配合して、冷感組成物含有または感覚刺激剤組成物含有香料組成物(以下、単に「本発明に係る香料組成物」または「香料組成物」とも呼ぶ)とし、この本発明に係る香料組成物を製品に配合することもできる。このとき、p-メンタン-3,8-ジオール、それ以外の冷感成分、及び温感成分を別々の香料組成物に添加し、それぞれの香料組成物を製品に混合するようにしてもよい。
本発明に係る香料組成物において、冷感組成物または感覚刺激剤組成物と共に含有し得る香料成分としては、各種の合成香料、天然精油、合成精油、柑橘油、動物性香料などを挙げることができ、例えば「周知・慣用技術集(香料)第I部」(平成11年1月29日、特許庁発行)に記載されているような広範な種類の香料成分を使用することができる。
そのうちでも代表的なものとしては、例えば、α-ピネン、リモネン、ネラール、ゲラニアール、2,5-ジメチル-4-ヒドロキシ-3(2H)-フラノン、バニリン、エチルバニリン、ゲラニオール、ネロール、シトロネロール、cis-3-ヘキセノール、フェニルエチルアルコール、スチラリルアセテート、オイゲノール、ローズオキサイド、リナロール、ベンズアルデヒド、ムスコン、ムスクT(高砂香料工業株式会社)、テサロン(高砂香料工業株式会社)などを挙げることができる。
つまり、該香料組成物においては、前記p-メンタン-3,8-ジオール異性体混合物を0.0001~90質量%含有することが好ましく、0.01~50質量%含有することが更に好ましい。
つまり、該香料組成物においては、前記p-メンタン-3,8-ジオール異性体混合物を0.0001~90質量%質量%含有することが好ましく、0.01~50質量%質量%含有することが更に好ましい。
本発明の冷感組成物または感覚刺激剤組成物及びそれらを含有する香料組成物によって、冷感または感覚刺激を付与することのできる飲食品の具体例としては、何ら限定されるものではないが、果汁飲料類、果実酒類、乳飲料類、炭酸飲料、清涼飲料、ドリンク剤類の如き飲料類;アイスクリーム類、シャーベット類、アイスキャンディー類の如き冷菓類;ゼリー、プリンなどのデザート類;ケーキ、クッキー、チョコレート、チューインガムなどの洋菓子類;饅頭、羊羹、ウイロウなどの和菓子類;ジャム類;キャンディー類;パン類;緑茶、ウーロン茶、紅茶、柿の葉茶、カミツレ茶、クマザサ茶、桑茶、ドクダミ茶、プアール茶、マテ茶、ルイボス茶、ギムネマ茶、グアバ茶、コーヒー、ココアの如き茶飲料または嗜好飲料類;和風スープ、洋風スープ、中華スープの如きスープ類;風味調味料;各種インスタント飲料などの食品類;各種スナック食品類などを挙げることができる。
本発明の冷感組成物または感覚刺激剤組成物及びそれらを含有する香料組成物によって香気付けすることのできる香粧品または日用雑貨品としては、例えば、フレグランス製品、基礎化粧品、仕上げ化粧品、頭髪化粧品、日焼け化粧品、薬用化粧品、ヘアケア製品、石鹸、身体洗浄剤、浴用剤、洗剤、柔軟仕上げ剤、洗浄剤、台所用洗剤、漂白剤、エアゾール剤、消臭及び/又は芳香剤、忌避剤、その他の雑貨類などを挙げることができる。
・フレグランス製品としては、香水、オードパルファム、オードトワレ、オーデコロンなど;
・基礎化粧品としては、洗顔クリーム、バニシングクリーム、クレンジングクリーム、コールドクリーム、マッサージクリーム、乳液、化粧水、美容液、パック、メイク落としなど;
・仕上げ化粧品としては、ファンデーション、粉おしろい、固形おしろい、タルカムパウダー、口紅、リップクリーム、頬紅、アイライナー、マスカラ、アイシャドウ、眉墨、アイパック、ネイルエナメル、エナメルリムバーなど;
・頭髪化粧品としては、ポマード、ブリランチン、セットローション、ヘアーステック、ヘアーソリッド、ヘアーオイル、ヘアートリートメント、ヘアークリーム、ヘアートニック、ヘアーリキッド、ヘアースプレー、バンドリン、養毛剤、染毛剤など;
を挙げることができる。
・薬用化粧品としては、制汗剤、アフターシェービングローション及びジェル、パーマネントウェーブ剤、薬用石鹸、薬用シャンプー、薬用皮膚化粧料などを挙げることができ;
・ヘアケア製品としては、シャンプー、リンス、リンスインシャンプー、コンディショナー、トリートメント、ヘアパックなど;
・石鹸としては、化粧石鹸、浴用石鹸、香水石鹸、透明石鹸、合成石鹸など;
・身体洗浄剤としては、ボディソープ、ボディシャンプー、ハンドソープなど;
・浴用剤としては、入浴剤(バスソルト、バスタブレット、バスリキッド等)、フォームバス(バブルバス等)、バスオイル(バスパフューム、バスカプセル等)、ミルクバス、バスジェリー、バスキューブなど;
・洗剤としては、衣料用重質洗剤、衣料用軽質洗剤、液体洗剤、洗濯石鹸、コンパクト洗剤、粉石鹸など;を挙げることができる。
・洗浄剤としては、クレンザー、ハウスクリーナー、トイレ洗浄剤、浴室用洗浄剤、ガラスクリーナー、カビ取り剤、排水管用洗浄剤など;
・台所用洗剤としては、台所用石鹸、台所用合成石鹸、食器用洗剤など;
・漂白剤としては、酸化型漂白剤(塩素系漂白剤、酸素系漂白剤等)、還元型漂白剤(硫黄系漂白剤等)、光学的漂白剤など;
・エアゾール剤としては、スプレータイプ、パウダースプレーなど;
・消臭及び/又は芳香剤としては、固形状タイプ、ゲル状タイプ、リキッドタイプなど;
・忌避剤としては、乳剤、油剤、水和剤、噴霧剤、塗布剤、粉剤、粒剤、カプセル剤、シート剤など;
を挙げることができる。
・雑貨としては、ティッシュペーパー、トイレットペーパーなど;
を挙げることができる。
・口腔用組成物としては、例えば、歯磨き(練り歯磨剤、歯磨きジェル)、口腔洗浄料、マウスウオッシュ、トローチ、チューインガム類などを挙げることができる。
・医薬品類としては、ハップ剤、軟膏剤の如き皮膚外用剤、内服剤などを挙げることができる。
本発明の冷感組成物または感覚刺激剤組成物及びそれを含有する香料組成物を上記したような各種の製品の冷感または感覚刺激の付与に用いる場合は、冷感または感覚刺激が付与される製品の種類や製品の最終形態(例えば液体状、固体状、粉末状、ゲル状、ミスト状、エアゾール状などの製品形態)に応じて、冷感組成物または感覚刺激剤組成物或いはそれらを含有する冷感組成物または香料組成物を、そのまま直接製品に添加または付与してもよいし;冷感組成物または感覚刺激剤組成物或いはそれらを含有する冷感組成物または感覚刺激剤組成物含有香料組成物を、例えば、アルコール類、プロピレングリコール、グリセリンなどの多価アルコール類に溶解して液体状にして添加または付与してもよいし;アラビアガム、トラガントガムなどの天然ガム質類、界面活性剤(例えばグリセリン脂肪酸エステル、ショ糖脂肪酸エステルなどの非イオン界面活性剤、アニオン界面活性剤、カチオン界面活性剤、両性界面活性剤など)を用いて可溶化或いは乳化分散させた可溶化状或いは分散状にして添加または付与してもよいし;アラビアガム等の天然ガム質類、ゼラチン、デキストリンなどの賦形剤を用いて被膜形成した粉末状で添加または付与してもよいし;カプセル化剤で処理してマイクロカプセルにして添加または付与してもよい。さらに、サイクロデキストリンなどの包接剤に包接して、冷感組成物または感覚刺激剤組成物或いはそれらを含有する香料組成物を安定化すると共に徐放性にして用いてもよい。
つまり、該製品においては、前記p-メンタン-3,8-ジオール異性体混合物を0.0001~90質量%含有することが好ましく、0.01~20質量%含有することが更に好ましい。
GC:ジーエルサイエンス株式会社 GC-4000
有機層を水層から分離して回収した後、有機層を水で洗浄して分液、さらには有機層から溶媒を留去し、減圧蒸留にて(1S)体が全組成の99質量%を占める(さらに具体的には、(1S,3R,4S)体が全組成の66質量%、(1S,3S,4S)体が全組成の30質量%を占める)である(1S)-p-メンタン-3,8-ジオール異性体混合物67.5gを得た。
実施例1、実施例2、比較例1で得た(1S)-p-メンタン-3,8-ジオール異性体混合物、(1RS)-p-メンタン-3,8-ジオール異性体混合物、(1R)-p-メンタン-3,8-ジオール異性体混合物についてそれぞれ180ppm水溶液を調製した。10人の5年以上経験した専門パネラーにより、180ppm水溶液について口中で官能評価を行った。
即ち、比較例1における異性体混合物の冷感強度を3とした場合のp-メンタン-3,8-ジオール異性体混合物の相対的な平均冷感強度は表1のようになった。
実施例1、実施例2、比較例1で得た(1S)-p-メンタン-3,8-ジオール異性体混合物、(1RS)-p-メンタン-3,8-ジオール異性体混合物、(1R)-p-メンタン-3,8-ジオール異性体混合物についてそれぞれ180ppm水溶液を調製した。10人の5年以上経験した専門パネラーにより、180ppm水溶液について口中で官能評価を行った。
l-メントールと、実施例1で得た(1S)-p-メンタン-3,8-ジオール異性体混合物について、95:5(質量比)で混合し、冷感組成物を調製した。得られた冷感組成物について、それぞれ20ppmの水溶液を調製し、口中で官能評価を行うとともに、比較として、l-メントール単独の20ppm水溶液についても口中での官能評価を行った。
また、吐き出し後3分を経過しても、パネラー10名中8名が、(1S)-p-メンタン-3,8-ジオール異性体混合物を含むものが、メントール単独に比べて強い清涼性の持続感を有すると回答した。
実施例1で得た(1S)-p-メンタン-3,8-ジオール異性体混合物について、0.5質量%の温感成分バニリルブチルエーテルを含有した感覚刺激剤組成物を調製した。
調製された感覚刺激剤組成物について、それぞれ20ppmの水溶液1,000mlを調製し、口中で官能評価を行うとともに、比較として、(1S)-p-メンタン-3,8-ジオール異性体混合物単独の20ppm水溶液についても口中での官能評価を行った。
下記処方に従い、練り歯磨剤を調製した。
(成分) (配合量 g)
l-メントール 0.25
(1S)-p-メンタン-3,8-ジオール異性体混合物 0.05
リン酸水素カルシウム(2水和物) 50.00
グリセリン 25.00
ラウリル硫酸ナトリウム 1.40
カルボキシメチルセルロースナトリウム 1.50
サッカリンナトリウム 0.20
安息香酸ナトリウム 0.10
ストロベリータイプフレーバー(高砂香料工業株式会社製) 0.70
精製水 残部
合計 100.00
下記処方に従い、歯磨きジェルを調製した。
(成分) (配合量 g)
l-メントール 0.30
(1S)-p-メンタン-3,8-ジオール異性体混合物 0.01
炭酸水素ナトリウム 97.69
酸化マグネシウム 0.50
ポリエチレングリコール 0.50
サッカリンナトリウム 0.20
三リン酸ナトリウム 0.10
ペパーミントタイプフレーバー(高砂香料工業株式会社製) 0.70
合計 100.00
下記処方に従い、チューインガムを調製した。
(成分) (配合量 g)
l-メントール 0.01
(1S)-p-メンタン-3,8-ジオール異性体混合物 0.01
ガムベース 24.00
コーンシロップ(42DE) 6.70
グリセリン 1.10
砂糖 67.18
ペパーミントタイプフレーバー(高砂香料工業株式会社製) 1.00
合計 100.00
下記処方(配合量は質量部)に従い、常法により(1S)-p-メンタン-3,8-ジオール異性体混合物を含有する香料組成物を調製した。
(成分) (配合量 g)
アップルベース(高砂香料工業株式会社製) 8.0
ベルガモットオイル 14.0
アセト酢酸エチル 5.0
ジヒドロジャスモン酸メチル 23.0
ラウリナール 3.0
レボサンドール(高砂香料工業株式会社製) 4.0
オレンジオイル 8.0
10-オキサ-16-ヘキサデカノライド 8.0
フェノキサノール(IFF社製) 6.0
スチラリルアセテート 3.0
テサロン(高砂香料工業株式会社製) 8.0
(1S)-p-メンタン-3,8-ジオール異性体混合物 30.0
下記処方に従い、上記実施例8の香料組成物を1.0%賦香したシャンプー100gを調製した。このものは、冷感を有しかつ冷感効果を持続した。
(成分) (配合量 g)
ポリオキシエチレンラウリルエーテル硫酸ナトリウム 14.00
ラウリン酸アミドプロピルベタイン 4.00
ヤシ油脂肪酸ジエタノールアミド 3.00
カチオン化セルロース 0.50
ジステアリン酸エチレングリコール 1.00
パラオキシ安息香酸エチル 0.25
クエン酸 適量
実施例8の香料組成物 1.00
精製水 残部
合計 100.00
下記処方(配合量は質量部)に従い、常法により(1S)-p-メンタン-3,8-ジオール異性体混合物を含有する感覚刺激剤組成物を調製した。
(成分) (配合量 g)
(1S)-p-メンタン-3,8-ジオール異性体混合物 50.00
2-(メントキシ)エタノール 20.00
3-ヒドロキシブタン酸メンチル 15.00
3-メントキシプロパン-1,2-ジオール 10.00
イソプレゴール 4.89
スピラントール 0.10
バニリルエチルエーテル 0.01
合計 100.00
下記処方に従い、チューインガムを調製した。
(成分) (配合量 g)
l-メントール 0.01
実施例10の感覚刺激剤組成物 0.01
ガムベース 24.00
コーンシロップ(42DE) 6.70
グリセリン 1.10
砂糖 67.18
ペパーミントタイプフレーバー(高砂香料工業株式会社製) 1.00
合計 100.00
Claims (10)
- 50質量%以上が(1S)体で構成されるp-メンタン-3,8-ジオール異性体混合物を含有する冷感組成物。
- p-メンタン-3,8-ジオール異性体混合物中の(1S,3R,4S)体:(1R,3S,4R)体の質量比が50:50~99.5:0.5である、請求項1に記載の冷感組成物。
- 90質量%以上が(1S,3R,4S)体及び(1S,3S,4S)体で構成されるp-メンタン-3,8-ジオール異性体混合物を含有する請求項1又は2に記載の冷感組成物。
- さらに、メントール、イソプレゴール、メントン、カンファー、プレゴール、シネオール、ハッカオイル、3-メントキシプロパン-1,2-ジオール、N-アルキル-p-メンタン-3-カルボキサミド、3-メントキシ-2-メチルプロパン-1,2-ジオール、2-(メントキシ)エタノール、2-メチル-3-(l-メントキシ)プロパン-1,2-ジオール、3-メントキシプロパン-1-オール、4-l-メントキシブタン-1-オール、3-ヒドロキシブタン酸メンチル、1-(2-ヒドロキシ-4-メチルシクロヘキシル)-エタノン、乳酸メンチル、メントールグリセリンケタール、N-メチル-2,2-イソプロピルメチル-3-メチルブタンアミド、グリオキシル酸メンチル、コハク酸メンチル、グルタル酸メンチル、ペパーミントオイル、スペアーミントオイル、ユーカリプタスオイル、ハッカ油、ペパーミント及びスペアミントからなる群から選ばれる少なくとも1種以上の冷感成分を含有する請求項1~3のいずれかに記載の冷感組成物。
- 請求項1~4のいずれかに記載の冷感組成物と、
カプサイシン、ジンゲロール、バニリルブチルエーテル、バニリルエチルエーテル、バニリルプロピルエーテル、4-(l-メントキシメチル)-2-フェニル-1,3-ジオキソラン、4-(l-メントキシメチル)-2-(3’,4’-ジヒドロキシフェニル)-1,3-ジオキソラン、4-(l-メントキシメチル)-2-(2’-ヒドロキシ-3’-メトキシフェニル)-1,3-ジオキソラン、4-(l-メントキシ-メチル)-2-(4’-メトキシフェニル)-1,3-ジオキソラン、4-(l-メントキシメチル)-2-(3’,4’-メチレンジオキシフェニル)-1,3-ジオキソラン、4-(l-メトキシメチル)-2-(3’-メトキシ-4’-ヒドロキシフェニル)-1,3-ジオキソラン、バニリンアセタール類、トウガラシ油、トウガラシオレオレジン、ジンジャーオレオレジン、ノニル酸バニリルアミド、ジャンブーオレオレジン、サンショウエキス、サンショール-I、サンショール-II、サンショウアミド、黒胡椒エキス、カビシン、ピペリン及びスピラントールからなる群から選ばれる少なくとも1種以上の温感成分と、を含有する感覚刺激剤組成物。 - 請求項1~4のいずれかに記載の冷感組成物、又は、請求項5に記載の感覚刺激剤組成物を含有する香料組成物、飲食品、香粧品、日用雑貨品、口腔用組成物または医薬品。
- 50質量%以上が(1S)体で構成されるp-メンタン-3,8-ジオール異性体混合物。
- (1S,3R,4S)体:(1R,3S,4R)体の質量比が50:50~99.5:0.5である請求項7記載のp-メンタン-3,8-ジオール異性体混合物。
- (1S,3R,4S)体及び(1S,3S,4S)体が全組成の90質量%以上である請求項7又は8記載のp-メンタン-3,8-ジオール異性体混合物。
- 請求項7~9のいずれかに記載のp-メンタン-3,8-ジオール異性体混合物を0.0001~90質量%を含有する香料組成物、飲食品、香粧品、日用雑貨品、口腔用組成物または医薬品。
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| US14/239,831 US20140219931A1 (en) | 2011-08-31 | 2012-08-31 | P-menthane-3,8-diol isomer mixture, cooling sensation composition comprising the same, and product comprising the cooling sensation composition |
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|---|---|---|---|
| JP2011-189515 | 2011-08-31 | ||
| JP2011189515 | 2011-08-31 |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2725900A4 (en) * | 2011-06-30 | 2015-08-05 | Takasago Perfumery Co Ltd | ANTIMICROBIAL COMPOSITION |
| JP2018507864A (ja) * | 2015-02-24 | 2018-03-22 | 高砂香料工業株式会社 | 増強香料組成物 |
| JP2019216614A (ja) * | 2018-06-15 | 2019-12-26 | 国立研究開発法人農業・食品産業技術総合研究機構 | メントールの刺激抑制剤および刺激抑制方法 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107028813A (zh) * | 2017-04-18 | 2017-08-11 | 新疆中草堂医药科技有限公司 | 紫苏精油在制备口腔护理品中的应用 |
| US20220110847A1 (en) * | 2019-01-17 | 2022-04-14 | Takasago International Corporation | Use of cooling materials for the reduction or inhibition of saltiness in orally administered, imbibed or ingested consumer products |
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| JP2000154395A (ja) * | 1998-11-19 | 2000-06-06 | Takasago Internatl Corp | 呈味改善剤、該改善剤を含む口腔用組成物、該改善剤を含む飲料、及び該改善剤を用いる飲料の呈味改善方法 |
| JP2007002005A (ja) * | 2005-06-21 | 2007-01-11 | Takasago Internatl Corp | 香料組成物 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4017758B2 (ja) * | 1998-08-04 | 2007-12-05 | 高砂香料工業株式会社 | 冷感剤組成物 |
| WO2009034352A1 (en) * | 2007-09-13 | 2009-03-19 | Ian Thomas Dell | Composition containing p-menthane-3, 8-diol and its use as insect repellent |
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2012
- 2012-08-31 JP JP2013531413A patent/JPWO2013031932A1/ja active Pending
- 2012-08-31 WO PCT/JP2012/072108 patent/WO2013031932A1/ja not_active Ceased
- 2012-08-31 US US14/239,831 patent/US20140219931A1/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000154395A (ja) * | 1998-11-19 | 2000-06-06 | Takasago Internatl Corp | 呈味改善剤、該改善剤を含む口腔用組成物、該改善剤を含む飲料、及び該改善剤を用いる飲料の呈味改善方法 |
| JP2007002005A (ja) * | 2005-06-21 | 2007-01-11 | Takasago Internatl Corp | 香料組成物 |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2725900A4 (en) * | 2011-06-30 | 2015-08-05 | Takasago Perfumery Co Ltd | ANTIMICROBIAL COMPOSITION |
| JP2018507864A (ja) * | 2015-02-24 | 2018-03-22 | 高砂香料工業株式会社 | 増強香料組成物 |
| US10876066B2 (en) | 2015-02-24 | 2020-12-29 | Takasago International Corporation | Enhanced perfume compositions |
| JP7048317B2 (ja) | 2015-02-24 | 2022-04-05 | 高砂香料工業株式会社 | 増強香料組成物 |
| JP2019216614A (ja) * | 2018-06-15 | 2019-12-26 | 国立研究開発法人農業・食品産業技術総合研究機構 | メントールの刺激抑制剤および刺激抑制方法 |
| JP2023024684A (ja) * | 2018-06-15 | 2023-02-16 | 国立研究開発法人農業・食品産業技術総合研究機構 | メントールの刺激抑制剤および刺激抑制方法 |
| JP7261419B2 (ja) | 2018-06-15 | 2023-04-20 | 国立研究開発法人農業・食品産業技術総合研究機構 | メントールの刺激抑制剤および刺激抑制方法 |
| JP7462238B2 (ja) | 2018-06-15 | 2024-04-05 | 国立研究開発法人農業・食品産業技術総合研究機構 | メントールの刺激抑制剤および刺激抑制方法 |
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| US20140219931A1 (en) | 2014-08-07 |
| JPWO2013031932A1 (ja) | 2015-03-23 |
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