GB1502680A - Compositions for application to or consumption by the human body and containing compounds having a physiological cooling effect - Google Patents
Compositions for application to or consumption by the human body and containing compounds having a physiological cooling effectInfo
- Publication number
- GB1502680A GB1502680A GB23947/75A GB2394775A GB1502680A GB 1502680 A GB1502680 A GB 1502680A GB 23947/75 A GB23947/75 A GB 23947/75A GB 2394775 A GB2394775 A GB 2394775A GB 1502680 A GB1502680 A GB 1502680A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compositions
- products
- water
- impregnated
- tobacco
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title abstract 9
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 238000001816 cooling Methods 0.000 title 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 6
- 241000208125 Nicotiana Species 0.000 abstract 4
- 235000002637 Nicotiana tabacum Nutrition 0.000 abstract 4
- 235000019504 cigarettes Nutrition 0.000 abstract 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 3
- 239000006210 lotion Substances 0.000 abstract 3
- 238000002360 preparation method Methods 0.000 abstract 3
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 abstract 2
- 235000010585 Ammi visnaga Nutrition 0.000 abstract 2
- 244000153158 Ammi visnaga Species 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 235000015218 chewing gum Nutrition 0.000 abstract 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 abstract 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 2
- 239000002304 perfume Substances 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 239000000344 soap Substances 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- 235000000346 sugar Nutrition 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- QTDIEDOANJISNP-UHFFFAOYSA-N 2-dodecoxyethyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOCCOS(O)(=O)=O QTDIEDOANJISNP-UHFFFAOYSA-N 0.000 abstract 1
- YCTDZYMMFQCTEO-UHFFFAOYSA-N 3-octene Chemical class CCCCC=CCC YCTDZYMMFQCTEO-UHFFFAOYSA-N 0.000 abstract 1
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 abstract 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical class [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 206010042496 Sunburn Diseases 0.000 abstract 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 abstract 1
- 229960001138 acetylsalicylic acid Drugs 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 239000000443 aerosol Substances 0.000 abstract 1
- 235000013334 alcoholic beverage Nutrition 0.000 abstract 1
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- 235000010210 aluminium Nutrition 0.000 abstract 1
- 229940069428 antacid Drugs 0.000 abstract 1
- 239000003159 antacid agent Substances 0.000 abstract 1
- 230000001458 anti-acid effect Effects 0.000 abstract 1
- 239000001273 butane Substances 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 230000001055 chewing effect Effects 0.000 abstract 1
- 229940112822 chewing gum Drugs 0.000 abstract 1
- 239000012141 concentrate Substances 0.000 abstract 1
- 235000009508 confectionery Nutrition 0.000 abstract 1
- 239000002537 cosmetic Substances 0.000 abstract 1
- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 abstract 1
- 239000000551 dentifrice Substances 0.000 abstract 1
- 239000002781 deodorant agent Substances 0.000 abstract 1
- 239000003599 detergent Substances 0.000 abstract 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid ester group Chemical class C(CCCCCCCCCCC)(=O)O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 abstract 1
- JZKFHQMONDVVNF-UHFFFAOYSA-N dodecyl sulfate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCOS(O)(=O)=O JZKFHQMONDVVNF-UHFFFAOYSA-N 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229960002179 ephedrine Drugs 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- 239000003889 eye drop Substances 0.000 abstract 1
- 229940012356 eye drops Drugs 0.000 abstract 1
- 238000005187 foaming Methods 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- OTTZHAVKAVGASB-UHFFFAOYSA-N hept-2-ene Chemical class CCCCC=CC OTTZHAVKAVGASB-UHFFFAOYSA-N 0.000 abstract 1
- ACGUYXCXAPNIKK-UHFFFAOYSA-N hexachlorophene Chemical group OC1=C(Cl)C=C(Cl)C(Cl)=C1CC1=C(O)C(Cl)=CC(Cl)=C1Cl ACGUYXCXAPNIKK-UHFFFAOYSA-N 0.000 abstract 1
- 229960004068 hexachlorophene Drugs 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 239000008311 hydrophilic ointment Substances 0.000 abstract 1
- -1 hydroxy, methyl Chemical group 0.000 abstract 1
- 235000015243 ice cream Nutrition 0.000 abstract 1
- 235000015110 jellies Nutrition 0.000 abstract 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical class [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 abstract 1
- 239000001095 magnesium carbonate Substances 0.000 abstract 1
- 235000011160 magnesium carbonates Nutrition 0.000 abstract 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical class [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 abstract 1
- 235000012254 magnesium hydroxide Nutrition 0.000 abstract 1
- 235000019793 magnesium trisilicate Nutrition 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 abstract 1
- 239000002324 mouth wash Substances 0.000 abstract 1
- 229940051866 mouthwash Drugs 0.000 abstract 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 abstract 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 abstract 1
- 210000000653 nervous system Anatomy 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 239000007968 orange flavor Substances 0.000 abstract 1
- 235000015205 orange juice Nutrition 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- MRDVEANIAFFFKJ-UHFFFAOYSA-N piperidine pyrrolidine Chemical compound N1CCCCC1.N1CCCC1.N1CCCC1 MRDVEANIAFFFKJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003755 preservative agent Substances 0.000 abstract 1
- 230000002335 preservative effect Effects 0.000 abstract 1
- 239000003380 propellant Substances 0.000 abstract 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 abstract 1
- 229940081974 saccharin Drugs 0.000 abstract 1
- 235000019204 saccharin Nutrition 0.000 abstract 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 239000002453 shampoo Substances 0.000 abstract 1
- 230000000391 smoking effect Effects 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 1
- 235000011182 sodium carbonates Nutrition 0.000 abstract 1
- 235000014214 soft drink Nutrition 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 230000004936 stimulating effect Effects 0.000 abstract 1
- 235000019505 tobacco product Nutrition 0.000 abstract 1
- 230000001256 tonic effect Effects 0.000 abstract 1
- 239000000606 toothpaste Substances 0.000 abstract 1
- 229940034610 toothpaste Drugs 0.000 abstract 1
- 230000000699 topical effect Effects 0.000 abstract 1
Classifications
-
- 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
- A23G3/00—Sweetmeats; Confectionery; Marzipan; Coated or filled products
- A23G3/34—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
- A23G3/36—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof 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
- 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
- A23L27/204—Aromatic 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
- A23L27/205—Heterocyclic compounds
- A23L27/2054—Heterocyclic compounds having nitrogen as the only hetero atom
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
- A24B15/34—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances containing a carbocyclic ring other than a six-membered aromatic ring
- A24B15/345—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances containing a carbocyclic ring other than a six-membered aromatic ring containing condensed rings
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
- A24B15/36—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances containing a heterocyclic ring
- A24B15/38—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances containing a heterocyclic ring having only nitrogen as hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/13—Monohydroxylic alcohols containing saturated rings
- C07C31/137—Monohydroxylic alcohols containing saturated rings polycyclic with condensed ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
-
- 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
- C11B9/0042—Essential oils; Perfumes compounds containing condensed hydrocarbon rings
- C11B9/0046—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Polymers & Plastics (AREA)
- Food Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nutrition Science (AREA)
- Inorganic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Cosmetics (AREA)
- Seasonings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Manufacture Of Tobacco Products (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cigarettes, Filters, And Manufacturing Of Filters (AREA)
- Non-Alcoholic Beverages (AREA)
- Medicinal Preparation (AREA)
- Confectionery (AREA)
- General Preparation And Processing Of Foods (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
1502680 Compositions for stimulating physiological cold-receptors WILKINSON SWORD Ltd 2 June 1976 [3 June 1975] 23947/75 Heading A5B [Also in Divisions A2, C2, C5 and C6] Products for application or consumption by the human body contain in an amount effective to stimulate the cold receptors of the nervous system of the body when brought into contact therewith upon use of the product, a compound of the formula RX wherein R is a saturated or monoethylenically unsaturated bicyclic hydrocarbon radical containing a total of 8 to 12 carbon atoms and selected from [3.3.1] bicycloheptanes, [2.2.1] bicycloheptanes and hept-5-enes and [2.2.2] bicyclooctanes and oct-5-enes containing 1 to 3 C 1-5 alkyl substituents; and X is a CH 2 OH, COOH, COOR 1 or CONR 2 R 3 group attached to said bicyclic radical at a 2-position, wherein R 1 is a hydroxyalkyl or hydroxyalkoxyalkyl radical of 2-4 carbon atoms. R 2 taken separately is H or C 1-5 alkyl: R 3 taken separately is H, C 1-5 alkyl, C 1-5 hydroxyalkyl or C 3-6 alkoxycarbonylalkyl with the proviso that when R 1 is H, then R 2 may also be C 3-6 cycloalkyl, phenyl or phenyl containing up to 2 hydroxy, methyl or methoxy substituents; and R 2 and R 3 when taken together, represent a C 4-5 alkylene group, the carbon chain of which may optionally contain an ether oxygen atom, and forming with the nitrogen to which they are attached, a piperidine pyrrolidine or morpholino group. The products may be personal care products e.g. a cosmetic, toilet lotion or dentifrice, or cleansing preparations such as soap or detergent compositions, or impregnated cleansing tissues, or toothpicks; or may be edible or potable products such as chewing gums and flavoured drinks; or smoking compositions or products e.g. tobacco compositions, cigarettes and filter - tipped cigarettes; or pharmaceutical compositions containing a pharmaceutically active ingredient. Examples are given for the following products containing compounds of formula RX as defined above: Example 14:- After shave lotion comprising ethanol, diethyl phthalate, perfume, propylene glycol and water; Example 15:- Cleansing tissue impregnated with glycerine perfume, water and triethanolamine lauryl sulphate; Example 16:- Toothpaste; Example 17:- Aerosol foaming shaving soap comprising stearic and lauric acids, triethanolamine and water in a butane propellant; Example 18:- Hair shampoo containing sodium lauryl ether sulphate; Example 19:- An impregnated toothpick; Example 20:- Soft drink concentrate of orange flavour. orange juice, saccharin, sugar, preservative and water; Example 21:-ethanolic toilet water; Example 22:- A soft sweet of icing sugar: Example 23:- Hydrophilic ointment; Example 24:- Deodorant composition of hexachlorophene in a perfumed base: Example 25:- Lipstick: Example 26:- Solid cologne; Example 27:- Hair tonic; Example 28:- Mouthwash composition; Example 29:- Talcum powder; Example 30:- Chewing gum; Example 31:- Impregnated tobacco: Example 32:- an impregnated tip for a filter-tipped cigarette. Other compositions or products described include alcoholic beverages, ice cream, jellies, bath oils and salts, sunburn lotions, eyedrops, medicaments which may be topical or internal (e.g. antacid preparation of sodium or magnesium carbonates, aluminium or magnesium hydroxides or trisilicates; and aspirin or ephedrine compositions), tobacco products such as cigarettes and pipe tobacco, chewing tobacco and snuff; and miscellaneous preparations such as water soluble adhesives for envelopes, labels and postage stamps.
Priority Applications (24)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB23947/75A GB1502680A (en) | 1975-06-03 | 1975-06-03 | Compositions for application to or consumption by the human body and containing compounds having a physiological cooling effect |
ZA763156A ZA763156B (en) | 1975-06-03 | 1976-05-26 | Flavour modification |
ZA763155A ZA763155B (en) | 1975-06-03 | 1976-05-26 | Improvements in or relating to compounds having a physiological action on the nervous system of the human body and compositions containing them |
CA253,491A CA1054441A (en) | 1975-06-03 | 1976-05-27 | Flavour modification |
DE19762623868 DE2623868A1 (en) | 1975-06-03 | 1976-05-28 | METHOD FOR TASTE MODIFICATION OF INGESTABLE SUBSTANCES AND TOBACCO |
AU14469/76A AU503510B2 (en) | 1975-06-03 | 1976-05-31 | Compounds having a physiological action onthe nervous system |
AU14468/76A AU1446876A (en) | 1975-06-03 | 1976-05-31 | Flavour modification |
IT23816/76A IT1060882B (en) | 1975-06-03 | 1976-05-31 | IMPROVEMENTS OF COMPOUNDS HAVING A REFRESHING PHYSIOLOGICAL ACTION AND COMPOSITIONS CONTAINING THEM |
IT23815/76A IT1060764B (en) | 1975-06-03 | 1976-05-31 | AROMAS MODIFIERS |
JP51064033A JPS51148040A (en) | 1975-06-03 | 1976-06-01 | Compound physiologically acting to nervous system and article containing same |
DE19762624504 DE2624504A1 (en) | 1975-06-03 | 1976-06-01 | COMPOUND OR OBJECTIVE WITH A STIMULATING EFFECT TO THE COLD RECEPTORS OF THE HUMAN NERVOUS SYSTEM |
LU75061A LU75061A1 (en) | 1975-06-03 | 1976-06-01 | |
NL7605914A NL7605914A (en) | 1975-06-03 | 1976-06-01 | PROCESS FOR PREPARING MATERIALS WITH A PHYSIOLOGICAL COOLING EFFECT. |
NL7605913A NL7605913A (en) | 1975-06-03 | 1976-06-01 | METHOD OF MODIFYING THE TASTE AND / OR SMELL OF ORAL USE MATERIALS. |
JP51064032A JPS51148074A (en) | 1975-06-03 | 1976-06-01 | Flavor improvement |
LU75062A LU75062A1 (en) | 1975-06-03 | 1976-06-01 | |
BR3484/76A BR7603484A (en) | 1975-06-03 | 1976-06-01 | PRODUCT MANUFACTURED FOR THE CONSUMER PRODUCT FOR PERSONAL CARE DENTIFRICIO LOCÃO FOR TOUCHER COSMETIC PREPARATION TOUCHER TOUCH TOUCH TOOTH CLEANER TOOTH TOBACCO MANUFACTURE OF TOBACCO OR CONTAINING TOBACCO TOBACCO IMPREGNATED CIGARETTE CIGARETTE CIGAR CIGARETTE CIGARIGANE |
FR7616607A FR2391722A1 (en) | 1975-06-03 | 1976-06-02 | IMPROVEMENTS TO COMPOUNDS EXERCISING A PHYSIOLOGICAL COLD ACTION ON THE NERVOUS SYSTEM OF THE HUMAN BODY AND COMPOSITIONS CONTAINING THIS |
FR7616608A FR2312971A1 (en) | 1975-06-03 | 1976-06-02 | FLAVOR MODIFICATION PROCESS AND MODIFIER COMPOUNDS |
IE1182/76A IE43232B1 (en) | 1975-06-03 | 1976-06-02 | Compositions for application to or consumption by the human body and containing compounds having a physiological cooling effect |
DK242876A DK242876A (en) | 1975-06-03 | 1976-06-02 | MEDIUM TO PROVIDE A PHYSIOLOGICAL COLD EFFECT ON THE SKIN OR MUCKS OF THE HUMAN BODY |
DK242776A DK242776A (en) | 1975-06-03 | 1976-06-02 | Flavor substance |
BE2055080A BE842516A (en) | 1975-06-03 | 1976-06-03 | CHANGING THE FLAVOR |
BE2055081A BE842517A (en) | 1975-06-03 | 1976-06-03 | IMPROVEMENTS IN COMPOUNDS EXERCISING A PHYSIOLOGICAL ACTION ON THE NERVOUS SYSTEM OF THE HUMAN BODY AND COMPOSITIONS CONTAINING THESE COMPOUNDS |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB23947/75A GB1502680A (en) | 1975-06-03 | 1975-06-03 | Compositions for application to or consumption by the human body and containing compounds having a physiological cooling effect |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1502680A true GB1502680A (en) | 1978-03-01 |
Family
ID=10203902
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23947/75A Expired GB1502680A (en) | 1975-06-03 | 1975-06-03 | Compositions for application to or consumption by the human body and containing compounds having a physiological cooling effect |
Country Status (14)
Country | Link |
---|---|
JP (2) | JPS51148074A (en) |
AU (2) | AU503510B2 (en) |
BE (2) | BE842516A (en) |
BR (1) | BR7603484A (en) |
CA (1) | CA1054441A (en) |
DE (2) | DE2623868A1 (en) |
DK (2) | DK242876A (en) |
FR (2) | FR2391722A1 (en) |
GB (1) | GB1502680A (en) |
IE (1) | IE43232B1 (en) |
IT (2) | IT1060882B (en) |
LU (2) | LU75062A1 (en) |
NL (2) | NL7605914A (en) |
ZA (2) | ZA763156B (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4288349A (en) | 1978-11-03 | 1981-09-08 | Naarden International N.V. | Perfume compositions containing 3,3-dimethylbicyclo-[2,2,1]-heptane-2-carboxylic acid as a perfume |
WO1988007364A1 (en) * | 1987-04-01 | 1988-10-06 | BIOGAL Gyógyszergyár | New medicated ointment, process for its production, means of application using said ointment and production of said ointment |
US6455080B1 (en) | 1997-12-29 | 2002-09-24 | Wm. Wrigley Jr., Company | Chewing gum containing controlled release acyclic carboxamide and method of making |
US6627233B1 (en) | 1997-09-18 | 2003-09-30 | Wm. Wrigley Jr. Company | Chewing gum containing physiological cooling agents |
EP1541044A1 (en) * | 2002-09-19 | 2005-06-15 | Japan Tobacco Inc. | Filter for cigarette |
WO2006084246A2 (en) * | 2005-02-04 | 2006-08-10 | Senomyx, Inc. | Aromatic amides and ureas and their uses as sweet and/or umami flavor modifiers, tastants and taste enhancers |
WO2007022651A1 (en) * | 2005-08-22 | 2007-03-01 | Givaudan Sa | Substituted bicyclo [2.2.2] oct/5-ene compounds and their use as cooling agents |
JP2007517493A (en) * | 2003-08-06 | 2007-07-05 | セノミックス、インコーポレイテッド | Novel flavors, flavor modifiers, taste agents, taste enhancers, umami and sweet taste agents, and / or their enhancers and uses |
EP1935252A1 (en) | 1997-09-18 | 2008-06-25 | WM. Wrigley Jr., Company | Chewing gum composition |
WO2008151460A3 (en) * | 2007-06-13 | 2010-04-01 | Givaudan Sa | Cooling compounds |
US7842324B2 (en) | 2005-06-15 | 2010-11-30 | Senomyx, Inc. | Bis-aromatic amides and their uses as sweet flavor modifiers, tastants, and taste enhancers |
EP2478777A1 (en) | 2005-12-23 | 2012-07-25 | Kraft Foods Global Brands LLC | Composition providing a cooling sensation substantially similar to that provided by menthol |
EP2559424A1 (en) | 2005-10-05 | 2013-02-20 | Kraft Foods Global Brands LLC | Cooling composition comprising trimethyl isopropyl butanamide |
US8784782B2 (en) | 2005-02-04 | 2014-07-22 | Senomyx, Inc. | Compounds comprising linked heteroaryl moieties and their use as novel umami flavor modifiers, tastants and taste enhancers for comestible compositions |
US9072313B2 (en) | 2006-04-21 | 2015-07-07 | Senomyx, Inc. | Comestible compositions comprising high potency savory flavorants, and processes for producing them |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL8003068A (en) * | 1980-05-28 | 1982-01-04 | Naarden & Shell Aroma Chem | PERFUME COMPOSITIONS AND PERFUMED MATERIALS AND ARTICLES CONTAINING ESTERS OF BICYCLIC MONOTERPEENIC ACIDS AS RAW MATERIAL. |
NL8601541A (en) * | 1986-06-13 | 1988-01-04 | Naarden International Nv | CYCLOHEXANE, CYCLOHEXENE AND CYCLOHEXADIENE, BICYCLO 2.2.1 HEPHANE AND BICYCLO 2.2.1 HEPTHENCARBONIC ACID ALKYL ESTERS, AND PERFUMED COMPOSITIONS AND PERFUMED PRODUCTS THAT COMBINED PERFUMED. |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3250815A (en) * | 1962-02-05 | 1966-05-10 | Universal Oil Prod Co | Bicyclo (2.2.1) heptyl carbinols |
FR1472947A (en) * | 1964-06-22 | 1967-03-17 | Du Pont | Bicyclo [2, 2, 2] -octenes and their preparation |
-
1975
- 1975-06-03 GB GB23947/75A patent/GB1502680A/en not_active Expired
-
1976
- 1976-05-26 ZA ZA763156A patent/ZA763156B/en unknown
- 1976-05-26 ZA ZA763155A patent/ZA763155B/en unknown
- 1976-05-27 CA CA253,491A patent/CA1054441A/en not_active Expired
- 1976-05-28 DE DE19762623868 patent/DE2623868A1/en active Pending
- 1976-05-31 IT IT23816/76A patent/IT1060882B/en active
- 1976-05-31 IT IT23815/76A patent/IT1060764B/en active
- 1976-05-31 AU AU14469/76A patent/AU503510B2/en not_active Expired
- 1976-05-31 AU AU14468/76A patent/AU1446876A/en not_active Expired
- 1976-06-01 BR BR3484/76A patent/BR7603484A/en unknown
- 1976-06-01 DE DE19762624504 patent/DE2624504A1/en not_active Withdrawn
- 1976-06-01 JP JP51064032A patent/JPS51148074A/en active Pending
- 1976-06-01 LU LU75062A patent/LU75062A1/xx unknown
- 1976-06-01 NL NL7605914A patent/NL7605914A/en not_active Application Discontinuation
- 1976-06-01 JP JP51064033A patent/JPS51148040A/en active Pending
- 1976-06-01 LU LU75061A patent/LU75061A1/xx unknown
- 1976-06-01 NL NL7605913A patent/NL7605913A/en unknown
- 1976-06-02 FR FR7616607A patent/FR2391722A1/en active Granted
- 1976-06-02 DK DK242876A patent/DK242876A/en unknown
- 1976-06-02 IE IE1182/76A patent/IE43232B1/en unknown
- 1976-06-02 DK DK242776A patent/DK242776A/en unknown
- 1976-06-02 FR FR7616608A patent/FR2312971A1/en active Granted
- 1976-06-03 BE BE2055080A patent/BE842516A/en unknown
- 1976-06-03 BE BE2055081A patent/BE842517A/en not_active IP Right Cessation
Cited By (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4288349A (en) | 1978-11-03 | 1981-09-08 | Naarden International N.V. | Perfume compositions containing 3,3-dimethylbicyclo-[2,2,1]-heptane-2-carboxylic acid as a perfume |
WO1988007364A1 (en) * | 1987-04-01 | 1988-10-06 | BIOGAL Gyógyszergyár | New medicated ointment, process for its production, means of application using said ointment and production of said ointment |
US7364761B2 (en) | 1997-09-18 | 2008-04-29 | Wm. Wrigley Jr. Company | Chewing gum containing physiological cooling agents and method of preparing |
US6627233B1 (en) | 1997-09-18 | 2003-09-30 | Wm. Wrigley Jr. Company | Chewing gum containing physiological cooling agents |
EP1935252A1 (en) | 1997-09-18 | 2008-06-25 | WM. Wrigley Jr., Company | Chewing gum composition |
US7078066B2 (en) | 1997-09-18 | 2006-07-18 | Wm. Wrigley Jr. Company | Chewing gum containing physiological cooling agents and method of making |
US6455080B1 (en) | 1997-12-29 | 2002-09-24 | Wm. Wrigley Jr., Company | Chewing gum containing controlled release acyclic carboxamide and method of making |
US7487782B2 (en) | 2002-09-19 | 2009-02-10 | Japan Tobacco Inc. | Cigarette filter |
EP1541044A4 (en) * | 2002-09-19 | 2005-11-16 | Japan Tobacco Inc | Filter for cigarette |
EP1541044A1 (en) * | 2002-09-19 | 2005-06-15 | Japan Tobacco Inc. | Filter for cigarette |
US7476399B2 (en) | 2003-08-06 | 2009-01-13 | Senomyx Inc. | Flavors, flavor modifiers, tastants, taste enhancers, umami or sweet tastants, and/or enhancers and use thereof |
JP2007330268A (en) * | 2003-08-06 | 2007-12-27 | Senomyx Inc | New flavor, flavor modifier, tastant, taste enhancer, delicious and sweet testant and/or enhancer and use thereof |
US11268952B2 (en) | 2003-08-06 | 2022-03-08 | Firmenich Incorporated | Flavors, flavor modifiers, tastants, taste enhancers, umami or sweet tastants, and/or enhancers and use thereof |
JP2007517493A (en) * | 2003-08-06 | 2007-07-05 | セノミックス、インコーポレイテッド | Novel flavors, flavor modifiers, taste agents, taste enhancers, umami and sweet taste agents, and / or their enhancers and uses |
US10557845B2 (en) | 2003-08-06 | 2020-02-11 | Firmenich Incorporated | Flavors, flavor modifiers, tastants, taste enhancers, umami or sweet tastants, and/or enhancers and use thereof |
US8735081B2 (en) | 2003-08-06 | 2014-05-27 | Senomyx, Inc. | T1R hetero-oligomeric taste receptors, cell lines that express said receptors, and taste compounds |
US10060909B2 (en) | 2003-08-06 | 2018-08-28 | Senomyx, Inc. | Flavors, flavor modifiers, tastants, taste enhancers, umami or sweet tastants, and/or enhancers and use thereof |
US9459250B2 (en) | 2003-08-06 | 2016-10-04 | Senomyx, Inc. | Use of T1R3 venus flytrap region polypeptide to screen for taste modulators |
US7888470B2 (en) | 2003-08-06 | 2011-02-15 | Senomyx, Inc. | Chimeric T1R taste receptor polypeptides and nucleic acid sequences encoding and cell lines that express said chimeric T1R polypeptides |
US8895050B2 (en) | 2003-08-06 | 2014-11-25 | Senomyx, Inc. | Flavors, flavor modifiers, tastants, taste enhancers, umami or sweet tastants, and/or enhancers and use thereof |
US8124121B2 (en) | 2003-08-06 | 2012-02-28 | Senomyx, Inc. | Flavors, flavor modifiers, tastants, taste enhancers, umami or sweet tastants, and/or enhancers and use thereof |
US10352929B2 (en) | 2003-08-06 | 2019-07-16 | Senomyx, Inc. | T1R hetero-oligomeric taste receptors, cell lines that express said receptors, and taste compounds |
US8784782B2 (en) | 2005-02-04 | 2014-07-22 | Senomyx, Inc. | Compounds comprising linked heteroaryl moieties and their use as novel umami flavor modifiers, tastants and taste enhancers for comestible compositions |
US8968708B2 (en) | 2005-02-04 | 2015-03-03 | Senomyx, Inc. | Compounds comprising linked heteroaryl moieties and their use as novel umami flavor modifiers, tastants and taste enhancers for comestible compositions |
WO2006084246A3 (en) * | 2005-02-04 | 2007-01-25 | Senomyx Inc | Aromatic amides and ureas and their uses as sweet and/or umami flavor modifiers, tastants and taste enhancers |
WO2006084246A2 (en) * | 2005-02-04 | 2006-08-10 | Senomyx, Inc. | Aromatic amides and ureas and their uses as sweet and/or umami flavor modifiers, tastants and taste enhancers |
US7842324B2 (en) | 2005-06-15 | 2010-11-30 | Senomyx, Inc. | Bis-aromatic amides and their uses as sweet flavor modifiers, tastants, and taste enhancers |
WO2007022651A1 (en) * | 2005-08-22 | 2007-03-01 | Givaudan Sa | Substituted bicyclo [2.2.2] oct/5-ene compounds and their use as cooling agents |
EP2559424A1 (en) | 2005-10-05 | 2013-02-20 | Kraft Foods Global Brands LLC | Cooling composition comprising trimethyl isopropyl butanamide |
EP2478777A1 (en) | 2005-12-23 | 2012-07-25 | Kraft Foods Global Brands LLC | Composition providing a cooling sensation substantially similar to that provided by menthol |
US9072313B2 (en) | 2006-04-21 | 2015-07-07 | Senomyx, Inc. | Comestible compositions comprising high potency savory flavorants, and processes for producing them |
US7959958B2 (en) | 2007-06-13 | 2011-06-14 | Givaudan, S.A. | Cooling compounds |
WO2008151460A3 (en) * | 2007-06-13 | 2010-04-01 | Givaudan Sa | Cooling compounds |
Also Published As
Publication number | Publication date |
---|---|
IT1060882B (en) | 1982-09-30 |
CA1054441A (en) | 1979-05-15 |
BE842517A (en) | 1976-12-03 |
LU75061A1 (en) | 1977-01-21 |
FR2312971B3 (en) | 1979-02-23 |
JPS51148074A (en) | 1976-12-18 |
AU1446976A (en) | 1977-12-08 |
JPS51148040A (en) | 1976-12-18 |
DE2623868A1 (en) | 1976-12-16 |
DE2624504A1 (en) | 1976-12-23 |
NL7605914A (en) | 1976-12-07 |
BE842516A (en) | 1976-12-03 |
NL7605913A (en) | 1976-12-07 |
LU75062A1 (en) | 1977-01-21 |
FR2391722A1 (en) | 1978-12-22 |
ZA763155B (en) | 1977-04-27 |
BR7603484A (en) | 1977-01-04 |
DK242776A (en) | 1976-12-04 |
AU1446876A (en) | 1977-12-08 |
IT1060764B (en) | 1982-09-30 |
AU503510B2 (en) | 1979-09-06 |
FR2312971A1 (en) | 1976-12-31 |
FR2391722B1 (en) | 1979-08-17 |
ZA763156B (en) | 1977-04-27 |
IE43232L (en) | 1976-12-03 |
IE43232B1 (en) | 1981-01-14 |
DK242876A (en) | 1976-12-04 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |