ES2274985T3 - Aromas quimicos mejorados. - Google Patents
Aromas quimicos mejorados. Download PDFInfo
- Publication number
- ES2274985T3 ES2274985T3 ES02752283T ES02752283T ES2274985T3 ES 2274985 T3 ES2274985 T3 ES 2274985T3 ES 02752283 T ES02752283 T ES 02752283T ES 02752283 T ES02752283 T ES 02752283T ES 2274985 T3 ES2274985 T3 ES 2274985T3
- Authority
- ES
- Spain
- Prior art keywords
- group
- methyl
- compound
- alkyl
- ring
- 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 - Lifetime
Links
- 239000000126 substance Substances 0.000 title description 32
- 150000001875 compounds Chemical class 0.000 claims abstract description 74
- 239000000203 mixture Substances 0.000 claims abstract description 63
- 239000003205 fragrance Substances 0.000 claims abstract description 33
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 28
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 22
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims abstract description 18
- 239000002304 perfume Substances 0.000 claims abstract description 18
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 17
- 235000013361 beverage Nutrition 0.000 claims abstract description 11
- 235000013405 beer Nutrition 0.000 claims abstract description 6
- 239000002386 air freshener Substances 0.000 claims abstract description 5
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 claims description 46
- 239000003599 detergent Substances 0.000 claims description 36
- -1 dimethyl cyclopropyl Chemical group 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 24
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 claims description 23
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 claims description 23
- 229930007744 linalool Natural products 0.000 claims description 23
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 claims description 22
- 239000004615 ingredient Substances 0.000 claims description 20
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 claims description 13
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 claims description 13
- 235000000484 citronellol Nutrition 0.000 claims description 13
- 150000002148 esters Chemical class 0.000 claims description 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 10
- 230000008569 process Effects 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 9
- 150000001412 amines Chemical class 0.000 claims description 8
- 239000000344 soap Substances 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 239000002671 adjuvant Substances 0.000 claims description 5
- 239000002781 deodorant agent Substances 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- 230000001166 anti-perspirative effect Effects 0.000 claims description 4
- 239000003213 antiperspirant Substances 0.000 claims description 4
- 235000020166 milkshake Nutrition 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 239000002537 cosmetic Substances 0.000 claims description 2
- 239000002453 shampoo Substances 0.000 claims description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 21
- 125000004434 sulfur atom Chemical group 0.000 claims 14
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims 14
- 239000004202 carbamide Substances 0.000 claims 7
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims 7
- 125000001475 halogen functional group Chemical group 0.000 claims 7
- 125000001424 substituent group Chemical group 0.000 claims 7
- 150000003568 thioethers Chemical class 0.000 claims 7
- 150000003573 thiols Chemical class 0.000 claims 7
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 5
- 239000007858 starting material Substances 0.000 claims 5
- 238000004061 bleaching Methods 0.000 claims 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
- LBQAJLBSGOBDQF-UHFFFAOYSA-N nitro azanylidynemethanesulfonate Chemical compound [O-][N+](=O)OS(=O)(=O)C#N LBQAJLBSGOBDQF-UHFFFAOYSA-N 0.000 claims 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 claims 1
- 235000015122 lemonade Nutrition 0.000 claims 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-N sodium;hydron;carbonate Chemical compound [Na+].OC(O)=O UIIMBOGNXHQVGW-UHFFFAOYSA-N 0.000 claims 1
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical class CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 abstract description 15
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 abstract description 12
- 229940043350 citral Drugs 0.000 abstract description 12
- 239000000796 flavoring agent Substances 0.000 abstract description 12
- 235000019634 flavors Nutrition 0.000 abstract description 11
- 150000001241 acetals Chemical class 0.000 abstract description 9
- 239000007844 bleaching agent Substances 0.000 abstract description 7
- 238000004519 manufacturing process Methods 0.000 abstract description 7
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract description 6
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 abstract description 6
- 125000004036 acetal group Chemical group 0.000 abstract description 4
- 125000003172 aldehyde group Chemical group 0.000 abstract description 3
- 235000009508 confectionery Nutrition 0.000 abstract description 2
- 239000000645 desinfectant Substances 0.000 abstract description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical group COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 abstract 2
- 150000002825 nitriles Chemical group 0.000 abstract 2
- 239000000253 Denture Cleanser Substances 0.000 abstract 1
- 125000006575 electron-withdrawing group Chemical group 0.000 abstract 1
- 230000005923 long-lasting effect Effects 0.000 abstract 1
- 239000007937 lozenge Substances 0.000 abstract 1
- 239000003826 tablet Substances 0.000 abstract 1
- 235000019568 aromas Nutrition 0.000 description 23
- 239000000654 additive Substances 0.000 description 17
- 150000001299 aldehydes Chemical class 0.000 description 8
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 8
- 238000009472 formulation Methods 0.000 description 8
- 239000004094 surface-active agent Substances 0.000 description 8
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 229920001223 polyethylene glycol Polymers 0.000 description 7
- 238000001228 spectrum Methods 0.000 description 7
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 4
- 239000013256 coordination polymer Substances 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 235000000346 sugar Nutrition 0.000 description 4
- 239000006188 syrup Substances 0.000 description 4
- 235000020357 syrup Nutrition 0.000 description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- 235000005979 Citrus limon Nutrition 0.000 description 3
- 244000131522 Citrus pyriformis Species 0.000 description 3
- 241000402754 Erythranthe moschata Species 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 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 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
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- 239000000271 synthetic detergent Substances 0.000 description 3
- CZCBTSFUTPZVKJ-UHFFFAOYSA-N trans-Rosenoxid Natural products CC1CCOC(C=C(C)C)C1 CZCBTSFUTPZVKJ-UHFFFAOYSA-N 0.000 description 3
- 239000000341 volatile oil Substances 0.000 description 3
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- NUPSHWCALHZGOV-UHFFFAOYSA-N Decyl acetate Chemical compound CCCCCCCCCCOC(C)=O NUPSHWCALHZGOV-UHFFFAOYSA-N 0.000 description 2
- 239000005792 Geraniol Substances 0.000 description 2
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 206010020751 Hypersensitivity Diseases 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 description 2
- 241000234269 Liliales Species 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- ZYEMGPIYFIJGTP-UHFFFAOYSA-N O-methyleugenol Chemical compound COC1=CC=C(CC=C)C=C1OC ZYEMGPIYFIJGTP-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- BGRWYDHXPHLNKA-UHFFFAOYSA-N Tetraacetylethylenediamine Chemical compound CC(=O)N(C(C)=O)CCN(C(C)=O)C(C)=O BGRWYDHXPHLNKA-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
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- 230000000172 allergic effect Effects 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
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- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
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Classifications
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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
- C11B9/003—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing less than six carbon atoms
-
- 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
-
- 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
- A23L27/205—Heterocyclic compounds
- A23L27/2052—Heterocyclic compounds having oxygen or sulfur as the only hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/69—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to carbon-to-carbon double or triple bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/02—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen
- C07C47/105—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen containing rings
- C07C47/11—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen containing rings monocyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/21—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/225—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/28—Saturated compounds having —CHO groups bound to carbon atoms of rings other than six—membered aromatic rings
- C07C47/293—Saturated compounds having —CHO groups bound to carbon atoms of rings other than six—membered aromatic rings with three- or four-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/28—Saturated compounds having —CHO groups bound to carbon atoms of rings other than six—membered aromatic rings
- C07C47/34—Saturated compounds having —CHO groups bound to carbon atoms of rings other than six—membered aromatic rings polycyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/38—Unsaturated compounds having —CHO groups bound to carbon atoms of rings other than six—membered aromatic rings
- C07C47/45—Unsaturated compounds having —CHO groups bound to carbon atoms of rings other than six—membered aromatic rings having unsaturation outside the rings
-
- 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
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
- C11B9/0076—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing less than six atoms
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nutrition Science (AREA)
- Health & Medical Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Wood Science & Technology (AREA)
- Fats And Perfumes (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Cosmetics (AREA)
- Confectionery (AREA)
- Compositions Of Macromolecular Compounds (AREA)
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Applications Claiming Priority (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US34215001P | 2001-12-19 | 2001-12-19 | |
| US342150P | 2001-12-19 | ||
| US34858002P | 2002-01-15 | 2002-01-15 | |
| US348580P | 2002-01-15 | ||
| US35505202P | 2002-02-07 | 2002-02-07 | |
| US37791402P | 2002-05-03 | 2002-05-03 | |
| US377914P | 2002-05-03 | ||
| US38929802P | 2002-06-17 | 2002-06-17 | |
| US389298P | 2002-06-17 | ||
| US355052P | 2002-07-02 | ||
| PCT/US2002/022120 WO2003053902A1 (en) | 2001-12-19 | 2002-07-12 | Improved aromachemicals |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2274985T3 true ES2274985T3 (es) | 2007-06-01 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES02752283T Expired - Lifetime ES2274985T3 (es) | 2001-12-19 | 2002-07-12 | Aromas quimicos mejorados. |
Country Status (10)
| Country | Link |
|---|---|
| EP (2) | EP1458666B1 (enExample) |
| JP (2) | JP2006506316A (enExample) |
| AT (1) | ATE338017T1 (enExample) |
| AU (5) | AU2002318237A1 (enExample) |
| CA (2) | CA2469602A1 (enExample) |
| DE (1) | DE60214427T2 (enExample) |
| DK (1) | DK1458666T3 (enExample) |
| ES (1) | ES2274985T3 (enExample) |
| GB (1) | GB2383327B (enExample) |
| WO (4) | WO2003053902A1 (enExample) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7309795B2 (en) | 2001-12-19 | 2007-12-18 | Luca Turin | Citral derivatives |
| US7342042B2 (en) | 2001-12-19 | 2008-03-11 | Flexitral, Inc. | Lily of the valley aromachemicals |
| WO2003053902A1 (en) * | 2001-12-19 | 2003-07-03 | Flexitral, Inc. | Improved aromachemicals |
| MX2007007467A (es) * | 2004-12-22 | 2007-10-15 | Flexitral Inc | Derivados mejorados de citral y citronelal. |
| GB0428306D0 (en) * | 2004-12-24 | 2005-01-26 | Givaudan Sa | Compound |
| WO2006087571A2 (en) * | 2005-02-17 | 2006-08-24 | Flexitral Inc. | Aromachemicals |
| JP2008532947A (ja) * | 2005-03-02 | 2008-08-21 | フレクシトラル・インコーポレーテッド | 大環状チイラン |
| US7485668B2 (en) | 2005-04-14 | 2009-02-03 | International Flavors & Fragrances Inc. | Cyclopropanated macrocyclic ketones and lactones |
| CN101258140A (zh) * | 2005-04-19 | 2008-09-03 | 佛莱克特瑞尔公司 | 苯并（b）环丙（d）吡喃-2-（1h）-酮衍生物 |
| JP4745914B2 (ja) * | 2005-12-01 | 2011-08-10 | 花王株式会社 | 毛髪洗浄剤 |
| WO2007117462A1 (en) * | 2006-04-03 | 2007-10-18 | Flexitral, Inc. | Cyclopropanated aromachemicals |
| EP2041062A1 (en) * | 2006-04-03 | 2009-04-01 | Flexitral, Inc. | Aromachemicals |
| ES2396126T3 (es) | 2008-04-15 | 2013-02-19 | Eisai R&D Management Co., Ltd. | Compuesto de 3-fenilpirazol[5,1-b]tiazol |
| CN105073698B (zh) * | 2013-03-12 | 2017-03-15 | 高砂香料工业株式会社 | 具有环丙烷环的化合物及包含其的香料组合物和/或芳香组合物 |
| JP6356431B2 (ja) * | 2014-02-20 | 2018-07-11 | アサヒビール株式会社 | 発酵麦芽飲料 |
| JP6356432B2 (ja) * | 2014-02-20 | 2018-07-11 | アサヒビール株式会社 | 発酵麦芽飲料 |
| US20170275262A1 (en) * | 2014-09-19 | 2017-09-28 | Tingwei Cai | Cyclopropane derivatives in flavor and fragrance compositions |
| JP6487685B2 (ja) * | 2014-12-03 | 2019-03-20 | アサヒビール株式会社 | 容器詰めアルコール飲料 |
| JP6091028B1 (ja) * | 2015-11-11 | 2017-03-08 | 花王株式会社 | シクロプロパン化合物 |
| WO2019037862A1 (de) * | 2017-08-24 | 2019-02-28 | Symrise Ag | Organoschwefelverbindungen als riech- und geschmackstoffe |
| CN109453091B (zh) * | 2019-01-02 | 2021-08-24 | 广东美宝化妆品有限公司 | 一种基于复合鲜花提取液的香水及其制备方法 |
| JP6744937B2 (ja) * | 2019-02-22 | 2020-08-19 | アサヒビール株式会社 | 容器詰めアルコール飲料 |
| CN114989057B (zh) * | 2022-07-25 | 2023-06-02 | 江西农业大学 | 一种柠檬醛基酰基硫脲衍生物及其制备方法和应用 |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1061732A (en) * | 1912-08-07 | 1913-05-13 | Julius Hirsh | Union suit. |
| US2938040A (en) * | 1957-09-09 | 1960-05-24 | Shell Oil Co | Epoxidation of unsaturated aldehydes |
| CH424765A (de) * | 1963-02-11 | 1966-11-30 | Firmenich & Cie | Verfahren zur Herstellung von ungesättigten Ketonen |
| GB1082364A (en) * | 1964-03-18 | 1967-09-06 | Unilever Ltd | Method for the preparation of linalool |
| GB1108268A (en) * | 1964-12-17 | 1968-04-03 | Unilever Ltd | Preparation of linalool oxide |
| US3470241A (en) * | 1968-02-05 | 1969-09-30 | Firmenich & Cie | Cyclopropane intermediates for irones |
| US3590053A (en) * | 1968-03-11 | 1971-06-29 | Givaudan Corp | Method of producing 3,7-dimethyl-6,7-epoxy-octan-1-al |
| BE754374A (fr) * | 1969-08-05 | 1971-02-04 | Hoffmann La Roche | Derives de propargyle |
| US3950429A (en) * | 1969-09-10 | 1976-04-13 | Givaudan Corporation | 2-Methylthio-myrtanal |
| US3770836A (en) * | 1970-06-15 | 1973-11-06 | Philip Morris Inc | Cyclopropyl cyclohexanes |
| US3926860A (en) * | 1974-01-28 | 1975-12-16 | Int Flavors & Fragrances Inc | Fragrance materials containing cis-2-n-pentyl cyclopropane-1-carboxylic acid |
| DE2617816A1 (de) * | 1976-04-23 | 1977-11-10 | Henkel & Cie Gmbh | Verwendung von epoxynitrilen als riechstoffe sowie diese enthaltende riechstoffkompositionen |
| US4097531A (en) * | 1976-06-04 | 1978-06-27 | Scm Corporation | Substituted cyclopropane process and product |
| US4151103A (en) * | 1977-07-28 | 1979-04-24 | Int Flavors & Fragrances Inc | {60 -Oxy(oxo) sulfides and uses thereof in perfumery and in perfumed articles |
| FR2543134B2 (fr) * | 1981-11-10 | 1986-08-08 | Roussel Uclaf | Nouveaux derives du cyclopropane, leur procede de preparation et leur application a la preparation de compositions parfumantes |
| FR2516076B1 (fr) * | 1981-11-10 | 1986-05-16 | Roussel Uclaf | Nouveaux derives du cyclopropane, leur procede de preparation et leur application a la preparation de compositions parfumantes |
| US4435428A (en) * | 1982-09-23 | 1984-03-06 | International Flavors & Fragrances Inc. | Use in augmenting or enhancing the aroma or taste of foodstuff or chewing gum with the methyl carbonate of 1-hydroxymethyl-2-heptanoyl cyclopropane |
| US4536583A (en) * | 1983-08-01 | 1985-08-20 | International Flavors & Fragrances Inc. | Process for preparing mixtures containing 8,9-epithio-1-p-menthene |
| US4658067A (en) * | 1985-05-08 | 1987-04-14 | International Flavors & Fragrances Inc. | Dialkylthioalkenes, dialkylthioalkylcycloalkenes and monoalkylthioalkenylcycloalkenes and organoleptic uses thereof |
| NL8502530A (nl) * | 1985-09-16 | 1987-04-16 | Naarden International Nv | Aroma- en parfumcomposities, gearomatiseerde voedings- en genotmiddelen, resp. geparfumeerde produkten die een of meer gesubstitueerde thiofenen als grondstof bevatten, alsmede gesubstitueerde thiofenen. |
| US5024847A (en) * | 1989-09-18 | 1991-06-18 | Basf K&F Corporation | Sulfur containing acyclic terpenes |
| DE69708368T2 (de) * | 1996-04-09 | 2002-09-26 | Givaudan S.A., Vernier-Geneve | Cyclopentanbutanolderivate als Duftstoffe |
| EP0801049B1 (en) * | 1996-04-09 | 2001-11-21 | Givaudan SA | Cyclopentanebutanol derivatives as odorants |
| US6051548A (en) * | 1998-11-05 | 2000-04-18 | International Flavors & Fragrances Inc. | Trimethylcyclohexenylcyclopropyl ketones perfume composition |
| EP1204320A2 (en) * | 1999-07-23 | 2002-05-15 | Bioparken AS | Novel juvenile hormone analogues and their use as antifouling agents |
| WO2003053902A1 (en) * | 2001-12-19 | 2003-07-03 | Flexitral, Inc. | Improved aromachemicals |
| JP2003252812A (ja) * | 2002-02-28 | 2003-09-10 | Nippon Zeon Co Ltd | シクロプロパン化合物および香料組成物 |
-
2002
- 2002-07-12 WO PCT/US2002/022120 patent/WO2003053902A1/en not_active Ceased
- 2002-07-12 AU AU2002318237A patent/AU2002318237A1/en not_active Abandoned
- 2002-07-12 CA CA002469602A patent/CA2469602A1/en not_active Abandoned
- 2002-07-12 EP EP02752283A patent/EP1458666B1/en not_active Expired - Lifetime
- 2002-07-12 DE DE60214427T patent/DE60214427T2/de not_active Expired - Fee Related
- 2002-07-12 JP JP2003554619A patent/JP2006506316A/ja active Pending
- 2002-07-12 AU AU2002366778A patent/AU2002366778A1/en not_active Abandoned
- 2002-07-12 AT AT02752283T patent/ATE338017T1/de not_active IP Right Cessation
- 2002-07-12 ES ES02752283T patent/ES2274985T3/es not_active Expired - Lifetime
- 2002-07-12 DK DK02752283T patent/DK1458666T3/da active
- 2002-07-12 WO PCT/US2002/022441 patent/WO2003053903A1/en not_active Ceased
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- 2002-08-20 EP EP02805502A patent/EP1458665A1/en not_active Withdrawn
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2009
- 2009-01-20 AU AU2009200217A patent/AU2009200217A1/en not_active Abandoned
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| AU2002323273A1 (en) | 2003-07-09 |
| WO2003053901A1 (en) | 2003-07-03 |
| DE60214427T2 (de) | 2007-04-26 |
| CA2469602A1 (en) | 2003-07-03 |
| AU2002332586A2 (en) | 2003-07-09 |
| WO2003053902A1 (en) | 2003-07-03 |
| DK1458666T3 (da) | 2006-11-27 |
| GB0219381D0 (en) | 2002-09-25 |
| CA2469604A1 (en) | 2003-07-03 |
| AU2002366778A2 (en) | 2003-07-09 |
| WO2003053903A1 (en) | 2003-07-03 |
| GB2383327A (en) | 2003-06-25 |
| DE60214427D1 (de) | 2006-10-12 |
| JP2006506316A (ja) | 2006-02-23 |
| GB2383327B (en) | 2004-12-08 |
| EP1458665A1 (en) | 2004-09-22 |
| JP2005513119A (ja) | 2005-05-12 |
| EP1458666B1 (en) | 2006-08-30 |
| AU2009200217A1 (en) | 2009-02-12 |
| EP1458666A1 (en) | 2004-09-22 |
| WO2003053887A1 (en) | 2003-07-03 |
| AU2002366778A1 (en) | 2003-07-09 |
| AU2002318237A1 (en) | 2003-07-09 |
| ATE338017T1 (de) | 2006-09-15 |
| AU2002332586B2 (en) | 2006-07-13 |
| AU2002332586A1 (en) | 2003-07-09 |
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