DE60224180T2 - Cycloalkancarbonsäurederivate als duftstoffe mit moschuscharakter - Google Patents
Cycloalkancarbonsäurederivate als duftstoffe mit moschuscharakter Download PDFInfo
- Publication number
- DE60224180T2 DE60224180T2 DE60224180T DE60224180T DE60224180T2 DE 60224180 T2 DE60224180 T2 DE 60224180T2 DE 60224180 T DE60224180 T DE 60224180T DE 60224180 T DE60224180 T DE 60224180T DE 60224180 T2 DE60224180 T2 DE 60224180T2
- Authority
- DE
- Germany
- Prior art keywords
- compound
- compounds
- dimethylcyclohexyl
- musk
- ethoxy
- 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
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- 150000002148 esters Chemical class 0.000 claims abstract description 41
- 239000003205 fragrance Substances 0.000 claims abstract description 25
- 239000000203 mixture Substances 0.000 claims abstract description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
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- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 17
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical class OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 claims description 9
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- MMEAVAVRZYNYFB-UHFFFAOYSA-N 1,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1CC1(C)C(O)=O MMEAVAVRZYNYFB-UHFFFAOYSA-N 0.000 claims description 2
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- JBDSSBMEKXHSJF-UHFFFAOYSA-N cyclopentanecarboxylic acid Chemical class OC(=O)C1CCCC1 JBDSSBMEKXHSJF-UHFFFAOYSA-N 0.000 claims 3
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- FVUGZKDGWGKCFE-UHFFFAOYSA-N 1-(2,3,8,8-tetramethyl-1,3,4,5,6,7-hexahydronaphthalen-2-yl)ethanone Chemical compound CC1(C)CCCC2=C1CC(C(C)=O)(C)C(C)C2 FVUGZKDGWGKCFE-UHFFFAOYSA-N 0.000 description 1
- VPKMGDRERYMTJX-CMDGGOBGSA-N 1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-1-penten-3-one Chemical compound CCC(=O)\C=C\C1C(C)=CCCC1(C)C VPKMGDRERYMTJX-CMDGGOBGSA-N 0.000 description 1
- 125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 description 1
- GELKGHVAFRCJNA-UHFFFAOYSA-N 2,2-Dimethyloxirane Chemical compound CC1(C)CO1 GELKGHVAFRCJNA-UHFFFAOYSA-N 0.000 description 1
- MZZRKEIUNOYYDF-UHFFFAOYSA-N 2,4-dimethylcyclohex-3-ene-1-carbaldehyde Chemical compound CC1C=C(C)CCC1C=O MZZRKEIUNOYYDF-UHFFFAOYSA-N 0.000 description 1
- FAQVGPWFQGGIPP-UHFFFAOYSA-N 2-(2-methylpropyl)quinoline Chemical compound C1=CC=CC2=NC(CC(C)C)=CC=C21 FAQVGPWFQGGIPP-UHFFFAOYSA-N 0.000 description 1
- LUZDYPLAQQGJEA-UHFFFAOYSA-N 2-Methoxynaphthalene Chemical compound C1=CC=CC2=CC(OC)=CC=C21 LUZDYPLAQQGJEA-UHFFFAOYSA-N 0.000 description 1
- HMKKIXGYKWDQSV-SDNWHVSQSA-N 2-Pentyl-3-phenyl-2-propenal Chemical compound CCCCC\C(C=O)=C/C1=CC=CC=C1 HMKKIXGYKWDQSV-SDNWHVSQSA-N 0.000 description 1
- CJBXHTMAMPXERG-UHFFFAOYSA-N 2-[1-(3,3-dimethylcyclohexyl)ethoxy]-2-methylpropan-1-ol Chemical compound OCC(C)(C)OC(C)C1CCCC(C)(C)C1 CJBXHTMAMPXERG-UHFFFAOYSA-N 0.000 description 1
- HMKKIXGYKWDQSV-UHFFFAOYSA-N 2-benzylideneheptanal Chemical compound CCCCCC(C=O)=CC1=CC=CC=C1 HMKKIXGYKWDQSV-UHFFFAOYSA-N 0.000 description 1
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 1
- ORMHZBNNECIKOH-UHFFFAOYSA-N 4-(4-hydroxy-4-methylpentyl)cyclohex-3-ene-1-carbaldehyde Chemical compound CC(C)(O)CCCC1=CCC(C=O)CC1 ORMHZBNNECIKOH-UHFFFAOYSA-N 0.000 description 1
- AUBLFWWZTFFBNU-UHFFFAOYSA-N 6-butan-2-ylquinoline Chemical compound N1=CC=CC2=CC(C(C)CC)=CC=C21 AUBLFWWZTFFBNU-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- GITDWIBIPJFPDK-UHFFFAOYSA-N 8-ethyl-1-oxaspiro[4.5]decan-2-one Chemical compound C1CC(CC)CCC11OC(=O)CC1 GITDWIBIPJFPDK-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 240000007436 Cananga odorata Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 240000002943 Elettaria cardamomum Species 0.000 description 1
- 208000027534 Emotional disease Diseases 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- YIKYNHJUKRTCJL-UHFFFAOYSA-N Ethyl maltol Chemical compound CCC=1OC=CC(=O)C=1O YIKYNHJUKRTCJL-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 235000018958 Gardenia augusta Nutrition 0.000 description 1
- 241000147041 Guaiacum officinale Species 0.000 description 1
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 1
- 235000010254 Jasminum officinale Nutrition 0.000 description 1
- 240000005385 Jasminum sambac Species 0.000 description 1
- HFJRKMMYBMWEAD-UHFFFAOYSA-N Lauraldehyde Natural products CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 1
- KVWWIYGFBYDJQC-GHMZBOCLSA-N Methyl dihydrojasmonate Chemical compound CCCCC[C@@H]1[C@@H](CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-GHMZBOCLSA-N 0.000 description 1
- 239000004783 Serene Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- AXMVYSVVTMKQSL-UHFFFAOYSA-N UNPD142122 Natural products OC1=CC=C(C=CC=O)C=C1O AXMVYSVVTMKQSL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- BJLXIEORMMUPSC-UHFFFAOYSA-N [2,2-dimethyl-3-(2-methyl-5-prop-1-en-2-ylcyclopenten-1-yl)propyl] cyclopropanecarboxylate Chemical compound CC(=C)C1CCC(C)=C1CC(C)(C)COC(=O)C1CC1 BJLXIEORMMUPSC-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 229940072717 alpha-hexylcinnamaldehyde Drugs 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 229940062909 amyl salicylate Drugs 0.000 description 1
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzenecarboxaldehyde Natural products O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- BTMVHUNTONAYDX-UHFFFAOYSA-N butyl propionate Chemical class CCCCOC(=O)CC BTMVHUNTONAYDX-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 235000005300 cardamomo Nutrition 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 description 1
- 229940117916 cinnamic aldehyde Drugs 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- NYNCZOLNVTXTTP-UHFFFAOYSA-N ethyl 2-(1,3-dioxoisoindol-2-yl)acetate Chemical compound C1=CC=C2C(=O)N(CC(=O)OCC)C(=O)C2=C1 NYNCZOLNVTXTTP-UHFFFAOYSA-N 0.000 description 1
- 229940073505 ethyl vanillin Drugs 0.000 description 1
- UAIZDWNSWGTKFZ-UHFFFAOYSA-L ethylaluminum(2+);dichloride Chemical compound CC[Al](Cl)Cl UAIZDWNSWGTKFZ-UHFFFAOYSA-L 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- IFYYFLINQYPWGJ-VIFPVBQESA-N gamma-Decalactone Natural products CCCCCC[C@H]1CCC(=O)O1 IFYYFLINQYPWGJ-VIFPVBQESA-N 0.000 description 1
- OALYTRUKMRCXNH-QMMMGPOBSA-N gamma-Nonalactone Natural products CCCCC[C@H]1CCC(=O)O1 OALYTRUKMRCXNH-QMMMGPOBSA-N 0.000 description 1
- PHXATPHONSXBIL-JTQLQIEISA-N gamma-Undecalactone Natural products CCCCCCC[C@H]1CCC(=O)O1 PHXATPHONSXBIL-JTQLQIEISA-N 0.000 description 1
- 229940020436 gamma-undecalactone Drugs 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 1
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 1
- 125000002350 geranyl group Chemical group [H]C([*])([H])/C([H])=C(C([H])([H])[H])/C([H])([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229940091561 guaiac Drugs 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000000171 lavandula angustifolia l. flower oil Substances 0.000 description 1
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000001627 myristica fragrans houtt. fruit oil Substances 0.000 description 1
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 239000001738 pogostemon cablin oil Substances 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 229930007790 rose oxide Natural products 0.000 description 1
- 239000010671 sandalwood oil Substances 0.000 description 1
- 239000001290 saussurea lappa clarke root oil Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N serine Chemical compound OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 description 1
- 229940071536 silver acetate Drugs 0.000 description 1
- BSWGGJHLVUUXTL-UHFFFAOYSA-N silver zinc Chemical compound [Zn].[Ag] BSWGGJHLVUUXTL-UHFFFAOYSA-N 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- LFSYLMRHJKGLDV-UHFFFAOYSA-N tetradecanolide Natural products O=C1CCCCCCCCCCCCCO1 LFSYLMRHJKGLDV-UHFFFAOYSA-N 0.000 description 1
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 1
- 229940117960 vanillin Drugs 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
- Medicines Containing Plant Substances (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP01113377 | 2001-06-01 | ||
| EP01113377A EP1262474A1 (en) | 2001-06-01 | 2001-06-01 | Cycloalkanecarboxylic acid derivatives as fragrants with musk characteristics |
| PCT/CH2002/000282 WO2002096852A1 (en) | 2001-06-01 | 2002-05-30 | Cycloalkanecarboxylic acid derivatives as fragrants with musk characteristics |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60224180D1 DE60224180D1 (de) | 2008-01-31 |
| DE60224180T2 true DE60224180T2 (de) | 2008-12-11 |
Family
ID=8177615
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60224180T Expired - Lifetime DE60224180T2 (de) | 2001-06-01 | 2002-05-30 | Cycloalkancarbonsäurederivate als duftstoffe mit moschuscharakter |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7390779B2 (https=) |
| EP (2) | EP1262474A1 (https=) |
| JP (1) | JP4200094B2 (https=) |
| CN (1) | CN1249014C (https=) |
| AT (1) | ATE381530T1 (https=) |
| BR (1) | BR0210098B1 (https=) |
| DE (1) | DE60224180T2 (https=) |
| ES (1) | ES2298366T3 (https=) |
| MX (1) | MXPA03010828A (https=) |
| WO (1) | WO2002096852A1 (https=) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0204919D0 (en) * | 2002-03-01 | 2002-04-17 | Cst Medical Ltd | Treatment of female sexual dysfunction |
| GB0227807D0 (en) * | 2002-11-29 | 2003-01-08 | Givaudan Sa | Improvements in or relating ot organic compounds |
| WO2004050595A1 (en) | 2002-11-29 | 2004-06-17 | Givaudan Sa | Aliphatic compounds as fragrants with musk characteristics |
| ES2265618T3 (es) * | 2003-03-19 | 2007-02-16 | Firmenich Sa | Compuestos odorantes. |
| DE10335053A1 (de) * | 2003-07-31 | 2005-02-24 | Symrise Gmbh & Co. Kg | Alicyclische Ester mit Moschusgeruch |
| GB0410134D0 (en) * | 2004-05-07 | 2004-06-09 | Givaudan Sa | Organic compounds |
| US20060133415A1 (en) * | 2004-12-21 | 2006-06-22 | Mueller Peter D | Wireless internetwork transfer apparatus, systems, and methods |
| MX2009004132A (es) * | 2006-10-24 | 2009-04-28 | Givaudan Sa | Composiciones para contrarrestar el mal olor. |
| MX2010002470A (es) * | 2007-09-07 | 2010-03-26 | Givaudan Sa | Derivados de dimetilciclohexilo como neutralizadores de malos olores. |
| JP5442356B2 (ja) * | 2009-08-11 | 2014-03-12 | 長谷川香料株式会社 | 脂肪族エステル類、該化合物を含有する香料組成物および該化合物の製造法 |
| EP2632554B1 (en) * | 2010-10-25 | 2017-01-04 | Symrise AG | Perfume |
| US10407378B2 (en) | 2014-04-21 | 2019-09-10 | Takasago International Corporation | Compound, and flavor and/or fragrance composition containing said compound |
| CN109069386B (zh) * | 2016-04-20 | 2022-02-25 | 株式会社 Lg 生活健康 | 香料组合物 |
| EP3691468A4 (en) | 2017-10-06 | 2021-10-20 | Cargill, Incorporated | EASILY SOLUBLE STEVIOL GLYCOSIDE COMPOSITIONS |
| CN107759445A (zh) * | 2017-11-23 | 2018-03-06 | 帕潘纳(北京)科技有限公司 | 一种制备1‑（3,3,‑二甲基环己基）乙醇的方法 |
| US20220049183A1 (en) | 2018-12-20 | 2022-02-17 | Symrise Ag | Alicyclic musk fragrance compounds |
| WO2020210118A1 (en) | 2019-04-06 | 2020-10-15 | Cargill, Incorporated | Sensory modifiers |
| CN115427388A (zh) | 2020-04-08 | 2022-12-02 | 西姆莱斯有限公司 | 用作香味化合物的新型酯 |
| CN111333509B (zh) * | 2020-04-14 | 2022-06-10 | 东莞波顿香料有限公司 | 苹果风味化合物及其制备方法和食品添加剂 |
| US20240392208A1 (en) | 2021-09-13 | 2024-11-28 | Symrise Ag | Cyclopropanated fragrance compounds |
| EP4514769B1 (en) * | 2022-04-29 | 2026-04-15 | Firmenich SA | Musky odorant |
| CN120858081A (zh) | 2023-03-30 | 2025-10-28 | 国际香料和香精公司 | 使用铜催化剂生产麝香香料中间体的方法 |
| CN118834120A (zh) | 2023-04-11 | 2024-10-25 | 国际香料和香精公司 | 使用AlCl3作为催化剂的用于制备麝香香精中间体的方法 |
| CN116589354B (zh) * | 2023-04-27 | 2025-02-18 | 江苏馨瑞香料有限公司 | 罗曼麝香的制备方法 |
| WO2025238055A1 (en) | 2024-05-15 | 2025-11-20 | International Flavors & Fragrances Inc. | Method for producing a musk fragrance intermediate using heterogeneous catalysts |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5166412A (en) * | 1990-08-28 | 1992-11-24 | Firmenich S.A. | Esters and their use in perfumery |
| US5767305A (en) * | 1997-04-03 | 1998-06-16 | International Flavors & Fragrances Inc. | Cyclopropyl carboxylic acid esters and uses thereof in imparting, augmenting and enhancing aromas |
| IL136019A0 (en) * | 1998-09-09 | 2001-05-20 | Firmenich & Cie | Esters with musky odor and their use in perfumery |
-
2001
- 2001-06-01 EP EP01113377A patent/EP1262474A1/en not_active Withdrawn
-
2002
- 2002-05-30 US US10/478,626 patent/US7390779B2/en not_active Expired - Lifetime
- 2002-05-30 ES ES02727147T patent/ES2298366T3/es not_active Expired - Lifetime
- 2002-05-30 MX MXPA03010828A patent/MXPA03010828A/es active IP Right Grant
- 2002-05-30 WO PCT/CH2002/000282 patent/WO2002096852A1/en not_active Ceased
- 2002-05-30 DE DE60224180T patent/DE60224180T2/de not_active Expired - Lifetime
- 2002-05-30 CN CNB028110048A patent/CN1249014C/zh not_active Expired - Lifetime
- 2002-05-30 JP JP2003500032A patent/JP4200094B2/ja not_active Expired - Lifetime
- 2002-05-30 BR BRPI0210098-3B1A patent/BR0210098B1/pt active IP Right Grant
- 2002-05-30 EP EP02727147A patent/EP1392640B1/en not_active Expired - Lifetime
- 2002-05-30 AT AT02727147T patent/ATE381530T1/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1392640B1 (en) | 2007-12-19 |
| US7390779B2 (en) | 2008-06-24 |
| JP4200094B2 (ja) | 2008-12-24 |
| BR0210098B1 (pt) | 2013-07-16 |
| JP2004535412A (ja) | 2004-11-25 |
| CN1249014C (zh) | 2006-04-05 |
| EP1262474A1 (en) | 2002-12-04 |
| ATE381530T1 (de) | 2008-01-15 |
| MXPA03010828A (es) | 2004-02-17 |
| ES2298366T3 (es) | 2008-05-16 |
| CN1512980A (zh) | 2004-07-14 |
| WO2002096852A1 (en) | 2002-12-05 |
| EP1392640A1 (en) | 2004-03-03 |
| BR0210098A (pt) | 2004-04-13 |
| DE60224180D1 (de) | 2008-01-31 |
| US20040234568A1 (en) | 2004-11-25 |
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