ES2699775T3 - Procedimiento para la preparación de metoximelonal - Google Patents
Procedimiento para la preparación de metoximelonal Download PDFInfo
- Publication number
- ES2699775T3 ES2699775T3 ES12772313T ES12772313T ES2699775T3 ES 2699775 T3 ES2699775 T3 ES 2699775T3 ES 12772313 T ES12772313 T ES 12772313T ES 12772313 T ES12772313 T ES 12772313T ES 2699775 T3 ES2699775 T3 ES 2699775T3
- Authority
- ES
- Spain
- Prior art keywords
- products
- methyl
- ingredients
- care
- lilial
- 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.)
- Active
Links
- 238000000034 method Methods 0.000 title claims abstract description 17
- 238000002360 preparation method Methods 0.000 title description 2
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 9
- 238000005949 ozonolysis reaction Methods 0.000 claims abstract description 7
- 238000003786 synthesis reaction Methods 0.000 claims abstract description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 238000005984 hydrogenation reaction Methods 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 2
- 239000003638 chemical reducing agent Substances 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 2
- QMXBURPYNWBMJR-UHFFFAOYSA-N 6-methoxy-2,6-dimethylheptanal Chemical compound COC(C)(C)CCCC(C)C=O QMXBURPYNWBMJR-UHFFFAOYSA-N 0.000 abstract description 3
- 230000002829 reductive effect Effects 0.000 abstract description 2
- 239000000047 product Substances 0.000 description 46
- 239000000203 mixture Substances 0.000 description 33
- 239000004615 ingredient Substances 0.000 description 30
- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 description 17
- 239000002304 perfume Substances 0.000 description 17
- 241000234269 Liliales Species 0.000 description 16
- 239000003205 fragrance Substances 0.000 description 10
- -1 for example Chemical compound 0.000 description 9
- 238000004140 cleaning Methods 0.000 description 7
- 239000002537 cosmetic Substances 0.000 description 6
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 5
- LOKPJYNMYCVCRM-UHFFFAOYSA-N 16-Hexadecanolide Chemical compound O=C1CCCCCCCCCCCCCCCO1 LOKPJYNMYCVCRM-UHFFFAOYSA-N 0.000 description 4
- OSOIQJGOYGSIMF-UHFFFAOYSA-N cyclopentadecanone Chemical compound O=C1CCCCCCCCCCCCCC1 OSOIQJGOYGSIMF-UHFFFAOYSA-N 0.000 description 4
- 239000003599 detergent Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000006467 substitution reaction Methods 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- NEHPIUGJDUWSRR-UHFFFAOYSA-N 1-(4-propan-2-ylcyclohexyl)ethanol Chemical compound CC(C)C1CCC(C(C)O)CC1 NEHPIUGJDUWSRR-UHFFFAOYSA-N 0.000 description 3
- YLIXVKUWWOQREC-UHFFFAOYSA-N 2-methyl-3-[4-(2-methylpropyl)phenyl]propanal Chemical compound CC(C)CC1=CC=C(CC(C)C=O)C=C1 YLIXVKUWWOQREC-UHFFFAOYSA-N 0.000 description 3
- OHRBQTOZYGEWCJ-UHFFFAOYSA-N 3-(3-propan-2-ylphenyl)butanal Chemical compound CC(C)C1=CC=CC(C(C)CC=O)=C1 OHRBQTOZYGEWCJ-UHFFFAOYSA-N 0.000 description 3
- ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- FZJUFJKVIYFBSY-UHFFFAOYSA-N bourgeonal Chemical compound CC(C)(C)C1=CC=C(CCC=O)C=C1 FZJUFJKVIYFBSY-UHFFFAOYSA-N 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- BOPPSUHPZARXTH-UHFFFAOYSA-N ocean propanal Chemical compound O=CC(C)CC1=CC=C2OCOC2=C1 BOPPSUHPZARXTH-UHFFFAOYSA-N 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 description 3
- FQTLCLSUCSAZDY-UHFFFAOYSA-N (+) E(S) nerolidol Natural products CC(C)=CCCC(C)=CCCC(C)(O)C=C FQTLCLSUCSAZDY-UHFFFAOYSA-N 0.000 description 2
- KHWTYGFHPHRQMP-UHFFFAOYSA-N (4-propan-2-ylcyclohexyl)methanol Chemical compound CC(C)C1CCC(CO)CC1 KHWTYGFHPHRQMP-UHFFFAOYSA-N 0.000 description 2
- MMLYERLRGHVBEK-XYOKQWHBSA-N (4e)-5,9-dimethyldeca-4,8-dienal Chemical compound CC(C)=CCC\C(C)=C\CCC=O MMLYERLRGHVBEK-XYOKQWHBSA-N 0.000 description 2
- GLZPCOQZEFWAFX-YFHOEESVSA-N (Z)-Geraniol Chemical compound CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 2
- YGFGZTXGYTUXBA-UHFFFAOYSA-N (±)-2,6-dimethyl-5-heptenal Chemical compound O=CC(C)CCC=C(C)C YGFGZTXGYTUXBA-UHFFFAOYSA-N 0.000 description 2
- AFABGHUZZDYHJO-UHFFFAOYSA-N 2-Methylpentane Chemical compound CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
- JFTSYAALCNQOKO-UHFFFAOYSA-N 3-(4-ethylphenyl)-2,2-dimethylpropanal Chemical compound CCC1=CC=C(CC(C)(C)C=O)C=C1 JFTSYAALCNQOKO-UHFFFAOYSA-N 0.000 description 2
- YXVSKJDFNJFXAJ-UHFFFAOYSA-N 4-cyclohexyl-2-methylbutan-2-ol Chemical compound CC(C)(O)CCC1=CC=CC=C1 YXVSKJDFNJFXAJ-UHFFFAOYSA-N 0.000 description 2
- ROWKJAVDOGWPAT-UHFFFAOYSA-N Acetoin Chemical compound CC(O)C(C)=O ROWKJAVDOGWPAT-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VCYVDHAWDPDCKW-UHFFFAOYSA-N Citrusal Chemical compound C1=CC(=O)OC2=C(CC(C)(C)C=O)C(OC)=CC=C21 VCYVDHAWDPDCKW-UHFFFAOYSA-N 0.000 description 2
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
- DUKPKQFHJQGTGU-UHFFFAOYSA-N Hexyl salicylic acid Chemical compound CCCCCCOC(=O)C1=CC=CC=C1O DUKPKQFHJQGTGU-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- NUQDJSMHGCTKNL-UHFFFAOYSA-N cyclohexyl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1CCCCC1 NUQDJSMHGCTKNL-UHFFFAOYSA-N 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000002979 fabric softener Substances 0.000 description 2
- IFYYFLINQYPWGJ-UHFFFAOYSA-N gamma-decalactone Chemical compound CCCCCCC1CCC(=O)O1 IFYYFLINQYPWGJ-UHFFFAOYSA-N 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 description 2
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 2
- WASNIKZYIWZQIP-AWEZNQCLSA-N nerolidol Natural products CC(=CCCC(=CCC[C@@H](O)C=C)C)C WASNIKZYIWZQIP-AWEZNQCLSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 2
- CRDAMVZIKSXKFV-FBXUGWQNSA-N (2-cis,6-cis)-farnesol Chemical compound CC(C)=CCC\C(C)=C/CC\C(C)=C/CO CRDAMVZIKSXKFV-FBXUGWQNSA-N 0.000 description 1
- 239000001414 (2E)-2-(phenylmethylidene)octanal Substances 0.000 description 1
- 239000000260 (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol Substances 0.000 description 1
- VSRVCSJJKWDZSH-UHFFFAOYSA-N (3-pentyloxan-4-yl) acetate Chemical compound CCCCCC1COCCC1OC(C)=O VSRVCSJJKWDZSH-UHFFFAOYSA-N 0.000 description 1
- 239000000456 (3S,6Z)-3,7,11-trimethyldodeca-1,6,10-trien-3-ol Substances 0.000 description 1
- KHLFMZDGADSQGR-ACCUITESSA-N (3e)-1-oxacyclohexadec-3-en-2-one Chemical compound O=C/1OCCCCCCCCCCCC\C=C\1 KHLFMZDGADSQGR-ACCUITESSA-N 0.000 description 1
- QVEOSYKPYFNQAZ-XYOKQWHBSA-N (4e)-4,8-dimethyldeca-4,9-dienal Chemical compound C=CC(C)CC\C=C(/C)CCC=O QVEOSYKPYFNQAZ-XYOKQWHBSA-N 0.000 description 1
- JIYIHILAGIZIMD-CLFYSBASSA-N (4z)-cyclopentadec-4-en-1-one Chemical compound O=C1CCCCCCCCCC\C=C/CC1 JIYIHILAGIZIMD-CLFYSBASSA-N 0.000 description 1
- FQTLCLSUCSAZDY-SDNWHVSQSA-N (6E)-nerolidol Chemical compound CC(C)=CCC\C(C)=C\CCC(C)(O)C=C FQTLCLSUCSAZDY-SDNWHVSQSA-N 0.000 description 1
- KRLBLPBPZSSIGH-CSKARUKUSA-N (6e)-3,7-dimethylnona-1,6-dien-3-ol Chemical compound CC\C(C)=C\CCC(C)(O)C=C KRLBLPBPZSSIGH-CSKARUKUSA-N 0.000 description 1
- ZGEHHVDYDNXYMW-UPHRSURJSA-N (8z)-cyclohexadec-8-en-1-one Chemical compound O=C1CCCCCCC\C=C/CCCCCC1 ZGEHHVDYDNXYMW-UPHRSURJSA-N 0.000 description 1
- KHQDWCKZXLWDNM-KPKJPENVSA-N (e)-2-ethyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-en-1-ol Chemical compound CC\C(CO)=C/CC1CC=C(C)C1(C)C KHQDWCKZXLWDNM-KPKJPENVSA-N 0.000 description 1
- RNLHVODSMDJCBR-SOFGYWHQSA-N (e)-3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-ol Chemical compound CC(O)C(C)\C=C\C1CC=C(C)C1(C)C RNLHVODSMDJCBR-SOFGYWHQSA-N 0.000 description 1
- JEMMOQLKGKUHKJ-UHFFFAOYSA-N 1-(2,3,8,8-tetramethyl-1,3,4,4a,5,6,7,8a-octahydronaphthalen-2-yl)ethanone Chemical compound C1CCC(C)(C)C2CC(C(C)=O)(C)C(C)CC21 JEMMOQLKGKUHKJ-UHFFFAOYSA-N 0.000 description 1
- KDPSHFVSTJYAJQ-UHFFFAOYSA-N 1-ethoxy-4-(2-methylbutan-2-yl)cyclohexane Chemical compound CCOC1CCC(C(C)(C)CC)CC1 KDPSHFVSTJYAJQ-UHFFFAOYSA-N 0.000 description 1
- PMKDAPPYGOWKLX-UHFFFAOYSA-N 1-methyl-3-(2-methylpropyl)cyclohexan-1-ol Chemical compound CC(C)CC1CCCC(C)(O)C1 PMKDAPPYGOWKLX-UHFFFAOYSA-N 0.000 description 1
- FYMOBFDUZIDKMI-UHFFFAOYSA-N 2,2-dimethyl-3-(3-methylphenyl)propan-1-ol Chemical compound CC1=CC=CC(CC(C)(C)CO)=C1 FYMOBFDUZIDKMI-UHFFFAOYSA-N 0.000 description 1
- VNGAHMPMLRTSLF-UHFFFAOYSA-N 2,2-dimethyl-3-phenylpropan-1-ol Chemical compound OCC(C)(C)CC1=CC=CC=C1 VNGAHMPMLRTSLF-UHFFFAOYSA-N 0.000 description 1
- UEGBWDUVDAKUGA-UHFFFAOYSA-N 2,6,10-trimethylundec-9-enal Chemical compound CC(C)=CCCC(C)CCCC(C)C=O UEGBWDUVDAKUGA-UHFFFAOYSA-N 0.000 description 1
- 229940029225 2,6-dimethyl-5-heptenal Drugs 0.000 description 1
- WRFXXJKURVTLSY-UHFFFAOYSA-N 2,6-dimethyloctan-2-ol Chemical compound CCC(C)CCCC(C)(C)O WRFXXJKURVTLSY-UHFFFAOYSA-N 0.000 description 1
- ZJZOLSQPHYEYOB-UHFFFAOYSA-N 2-(4-methylpent-3-enyl)cyclohexene-1-carbaldehyde Chemical compound CC(C)=CCCC1=C(C=O)CCCC1 ZJZOLSQPHYEYOB-UHFFFAOYSA-N 0.000 description 1
- DNRJTBAOUJJKDY-UHFFFAOYSA-N 2-Acetyl-3,5,5,6,8,8-hexamethyl-5,6,7,8- tetrahydronaphthalene Chemical compound CC(=O)C1=C(C)C=C2C(C)(C)C(C)CC(C)(C)C2=C1 DNRJTBAOUJJKDY-UHFFFAOYSA-N 0.000 description 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- IXQGCWUGDFDQMF-UHFFFAOYSA-N 2-Ethylphenol Chemical compound CCC1=CC=CC=C1O IXQGCWUGDFDQMF-UHFFFAOYSA-N 0.000 description 1
- ZHOOOLQOWQVYOE-UHFFFAOYSA-N 2-cyclohexylidene-2-phenylacetonitrile Chemical compound C=1C=CC=CC=1C(C#N)=C1CCCCC1 ZHOOOLQOWQVYOE-UHFFFAOYSA-N 0.000 description 1
- LDGVIXYITWDQFB-UHFFFAOYSA-N 2-methylideneheptanal Chemical compound CCCCCC(=C)C=O LDGVIXYITWDQFB-UHFFFAOYSA-N 0.000 description 1
- MWYGSCHWFNRSET-UHFFFAOYSA-N 2-pentylcyclopentan-1-ol Chemical compound CCCCCC1CCCC1O MWYGSCHWFNRSET-UHFFFAOYSA-N 0.000 description 1
- DLHQZZUEERVIGQ-UHFFFAOYSA-N 3,7-dimethyl-3-octanol Chemical compound CCC(C)(O)CCCC(C)C DLHQZZUEERVIGQ-UHFFFAOYSA-N 0.000 description 1
- ZJPKYCLAROITRY-UHFFFAOYSA-N 3-(1-ethoxyethoxy)-3,7-dimethylocta-1,6-diene Chemical compound CCOC(C)OC(C)(C=C)CCC=C(C)C ZJPKYCLAROITRY-UHFFFAOYSA-N 0.000 description 1
- RLEFOSDUWZYGOS-UHFFFAOYSA-N 3-(4-Isopropylphenyl)propanal Chemical compound CC(C)C1=CC=C(CCC=O)C=C1 RLEFOSDUWZYGOS-UHFFFAOYSA-N 0.000 description 1
- DDFGFKGJBOILQZ-GHMZBOCLSA-N 3-[(1S,5R)-6,6-dimethyl-2-bicyclo[3.1.1]hept-2-enyl]propanal Chemical compound C1[C@H]2C(C)(C)[C@@H]1CC=C2CCC=O DDFGFKGJBOILQZ-GHMZBOCLSA-N 0.000 description 1
- VSIXJPFQJMODCS-UHFFFAOYSA-N 3-methyl-4-phenylbutan-2-ol Chemical compound CC(O)C(C)CC1=CC=CC=C1 VSIXJPFQJMODCS-UHFFFAOYSA-N 0.000 description 1
- OXYRENDGHPGWKV-UHFFFAOYSA-N 3-methyl-5-phenylpentan-1-ol Chemical compound OCCC(C)CCC1=CC=CC=C1 OXYRENDGHPGWKV-UHFFFAOYSA-N 0.000 description 1
- NKMKFQCVDZVEJR-UHFFFAOYSA-N 3-methylcyclopentadec-5-en-1-one Chemical compound CC1CC=CCCCCCCCCCC(=O)C1 NKMKFQCVDZVEJR-UHFFFAOYSA-N 0.000 description 1
- MQBIZQLCHSZBOI-UHFFFAOYSA-N 4-(4-Methyl-3-pentenyl)-3-cyclohexene-1-carboxaldehyde Chemical compound CC(C)=CCCC1=CCC(C=O)CC1 MQBIZQLCHSZBOI-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
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- YVSNOTITPICPTB-UHFFFAOYSA-N 4-methyl-2-(2-methylpropyl)oxan-4-ol Chemical compound CC(C)CC1CC(C)(O)CCO1 YVSNOTITPICPTB-UHFFFAOYSA-N 0.000 description 1
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- ABRIMXGLNHCLIP-VURMDHGXSA-N 5-Cyclohexadecenone Chemical compound O=C1CCCCCCCCCC\C=C/CCC1 ABRIMXGLNHCLIP-VURMDHGXSA-N 0.000 description 1
- LODLFUCEWWWXPR-UHFFFAOYSA-N 5-methyl-2-pentan-2-yl-5-propyl-1,3-dioxane Chemical compound CCCC(C)C1OCC(C)(CCC)CO1 LODLFUCEWWWXPR-UHFFFAOYSA-N 0.000 description 1
- OSMLMQQJZVENMX-UHFFFAOYSA-N 6-butyl-2,4-dimethyl-3,6-dihydro-2h-pyran Chemical compound CCCCC1OC(C)CC(C)=C1 OSMLMQQJZVENMX-UHFFFAOYSA-N 0.000 description 1
- AZUVBPVDRHGGEP-UHFFFAOYSA-N 6a,9a-dimethyl-4,5,7,8,9,9a-hexahydro-6aH-dipyrrolo(2,3-b;3',2',1'-hi)indole Natural products CC(=C)C1CCC(C)=CCCC(C)=CCCC(C)=CC1O AZUVBPVDRHGGEP-UHFFFAOYSA-N 0.000 description 1
- AWAHFLZWCBUHMX-UHFFFAOYSA-N 7-(3-methylbutyl)-1,5-benzodioxepin-3-one Chemical compound O1CC(=O)COC2=CC(CCC(C)C)=CC=C21 AWAHFLZWCBUHMX-UHFFFAOYSA-N 0.000 description 1
- KQPGRKHBHURUAP-UHFFFAOYSA-N 7-propyl-1,5-benzodioxepin-3-one Chemical compound O1CC(=O)COC2=CC(CCC)=CC=C21 KQPGRKHBHURUAP-UHFFFAOYSA-N 0.000 description 1
- AQJANVUPNABWRU-UHFFFAOYSA-N 8,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalene-2-carbaldehyde Chemical compound C1C(C=O)CCC2=C1C(C)(C)CCC2 AQJANVUPNABWRU-UHFFFAOYSA-N 0.000 description 1
- RANVDUNFZBMTBK-UHFFFAOYSA-N Amyl salicylate Chemical compound CCCCCOC(=O)C1=CC=CC=C1O RANVDUNFZBMTBK-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- XRHCAGNSDHCHFJ-UHFFFAOYSA-N Ethylene brassylate Chemical compound O=C1CCCCCCCCCCCC(=O)OCCO1 XRHCAGNSDHCHFJ-UHFFFAOYSA-N 0.000 description 1
- WSTYNZDAOAEEKG-UHFFFAOYSA-N Mayol Natural products CC1=C(O)C(=O)C=C2C(CCC3(C4CC(C(CC4(CCC33C)C)=O)C)C)(C)C3=CC=C21 WSTYNZDAOAEEKG-UHFFFAOYSA-N 0.000 description 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
- FQTLCLSUCSAZDY-ATGUSINASA-N Nerolidol Chemical compound CC(C)=CCC\C(C)=C\CC[C@](C)(O)C=C FQTLCLSUCSAZDY-ATGUSINASA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 239000002262 Schiff base Substances 0.000 description 1
- 150000004753 Schiff bases Chemical class 0.000 description 1
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- OAKFACUIGQLOCA-UHFFFAOYSA-N [1-methyl-2-[(1,2,2-trimethyl-3-bicyclo[3.1.0]hexanyl)methyl]cyclopropyl]methanol Chemical compound OCC1(C)CC1CC1C(C)(C)C2(C)CC2C1 OAKFACUIGQLOCA-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000002386 air freshener Substances 0.000 description 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 description 1
- GUUHFMWKWLOQMM-NTCAYCPXSA-N alpha-hexylcinnamaldehyde Chemical compound CCCCCC\C(C=O)=C/C1=CC=CC=C1 GUUHFMWKWLOQMM-NTCAYCPXSA-N 0.000 description 1
- 229940072717 alpha-hexylcinnamaldehyde Drugs 0.000 description 1
- GUUHFMWKWLOQMM-UHFFFAOYSA-N alpha-n-hexylcinnamic aldehyde Natural products CCCCCCC(C=O)=CC1=CC=CC=C1 GUUHFMWKWLOQMM-UHFFFAOYSA-N 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- 229940062909 amyl salicylate Drugs 0.000 description 1
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 1
- 230000001166 anti-perspirative effect Effects 0.000 description 1
- 239000003213 antiperspirant Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- 229940019836 cyclamen aldehyde Drugs 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 230000002951 depilatory effect Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- KRJHRNUTLDTSKY-UHFFFAOYSA-N diethyl cyclohexane-1,4-dicarboxylate Chemical compound CCOC(=O)C1CCC(C(=O)OCC)CC1 KRJHRNUTLDTSKY-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000006735 epoxidation reaction Methods 0.000 description 1
- 150000002118 epoxides 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
- 229930002886 farnesol Natural products 0.000 description 1
- 229940043259 farnesol Drugs 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000834 fixative Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- ONKNPOPIGWHAQC-UHFFFAOYSA-N galaxolide Chemical compound C1OCC(C)C2=C1C=C1C(C)(C)C(C)C(C)(C)C1=C2 ONKNPOPIGWHAQC-UHFFFAOYSA-N 0.000 description 1
- IFYYFLINQYPWGJ-VIFPVBQESA-N gamma-Decalactone Natural products CCCCCC[C@H]1CCC(=O)O1 IFYYFLINQYPWGJ-VIFPVBQESA-N 0.000 description 1
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 1
- 239000002241 glass-ceramic Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- IPWBXORAIBJDDQ-UHFFFAOYSA-N methyl 2-hexyl-3-oxocyclopentane-1-carboxylate Chemical compound CCCCCCC1C(C(=O)OC)CCC1=O IPWBXORAIBJDDQ-UHFFFAOYSA-N 0.000 description 1
- 229940102398 methyl anthranilate Drugs 0.000 description 1
- 231100000243 mutagenic effect Toxicity 0.000 description 1
- 230000003505 mutagenic effect Effects 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- 229940034610 toothpaste Drugs 0.000 description 1
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 1
- DKZBBWMURDFHNE-UHFFFAOYSA-N trans-coniferylaldehyde Natural products COC1=CC(C=CC=O)=CC=C1O DKZBBWMURDFHNE-UHFFFAOYSA-N 0.000 description 1
- 239000001069 triethyl citrate Substances 0.000 description 1
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- 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
- C07C45/40—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with ozone; by ozonolysis
-
- 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
- C11B9/0007—Aliphatic compounds
- C11B9/0015—Aliphatic compounds containing oxygen as the only heteroatom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
- C07C2523/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals of the platinum group metals
- C07C2523/44—Palladium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Fats And Perfumes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Saccharide Compounds (AREA)
- Preparation Of Fruits And Vegetables (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/CN2011/080634 WO2013053102A1 (en) | 2011-10-11 | 2011-10-11 | Improvements in or relating to organic compounds |
| PCT/EP2012/070109 WO2013053787A1 (en) | 2011-10-11 | 2012-10-11 | Process for the preparation of methoxymelonal |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2699775T3 true ES2699775T3 (es) | 2019-02-12 |
Family
ID=47018204
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES12772313T Active ES2699775T3 (es) | 2011-10-11 | 2012-10-11 | Procedimiento para la preparación de metoximelonal |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US9701606B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2766333B1 (cg-RX-API-DMAC7.html) |
| JP (2) | JP6343236B2 (cg-RX-API-DMAC7.html) |
| BR (1) | BR112014008401B1 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2699775T3 (cg-RX-API-DMAC7.html) |
| IN (1) | IN2014CN02612A (cg-RX-API-DMAC7.html) |
| MX (1) | MX343612B (cg-RX-API-DMAC7.html) |
| SG (1) | SG11201400939YA (cg-RX-API-DMAC7.html) |
| WO (2) | WO2013053102A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2015106293A1 (en) | 2014-01-13 | 2015-07-16 | P2 Science, Inc. | Terpene-derived acids and esters and methods for preparing and using same |
| WO2015110505A1 (en) * | 2014-01-23 | 2015-07-30 | Givaudan Sa | Process for the production of 2,6-dimethylhept-5-enal by baeyer-villiger oxidation |
| CN103819335B (zh) * | 2014-02-24 | 2016-01-20 | 南京运华立太能源科技有限公司 | 一种2,6-二甲基-6-烷氧基（或羟基）庚醛的制备方法 |
| GB201409348D0 (en) * | 2014-05-27 | 2014-07-09 | Givaudan Sa | Perfume compositions |
| WO2015191706A1 (en) | 2014-06-10 | 2015-12-17 | P2 Science, Inc. | Terpene-derived compounds and methods for preparing and using same |
| JP6687547B2 (ja) * | 2014-06-20 | 2020-04-22 | ピー２ サイエンス，インコーポレイティド | 管式又は多管式反応器における膜オゾン分解 |
| US10668446B2 (en) | 2016-06-21 | 2020-06-02 | P2 Science, Inc. | Flow-through reactors for the continuous quenching of peroxide mixtures and methods comprising the same |
| US10696605B2 (en) | 2016-09-16 | 2020-06-30 | P2 Science, Inc. | Uses of vanadium to oxidize aldehydes and ozonides |
| EP3332642A1 (en) * | 2016-12-08 | 2018-06-13 | drom fragrances GmbH & Co. KG | Antibacterial perfuming composition |
| US11814350B2 (en) | 2018-10-19 | 2023-11-14 | P2 Science, Inc. | Methods for disproportionation quenching of ozonides |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB859568A (en) | 1956-04-09 | 1961-01-25 | Glidden Co | 2-substituted-2,6-dimethyl octane derivatives |
| NL7412622A (nl) * | 1974-09-24 | 1976-03-26 | Stork Brabant Bv | Rasterfilm en een werkwijze voor het vervaardi- gen van een zeefsjabloon onder toepassing van deze rasterfilm, alsmede aldus vervaardigde zeefsjabloon. |
| GB1555333A (en) * | 1975-05-29 | 1979-11-07 | Bush Boake Allen Ltd | Perfumery compositions comprising hydroxy- or alkoxy-substituted c9 alkanals alkanols and esters |
| JP5226304B2 (ja) | 2004-06-03 | 2013-07-03 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | ハリコンドリンｂ類似体の調製用中間体 |
| EP1764355A1 (en) * | 2005-09-16 | 2007-03-21 | Givaudan S.A. | 6-methoxy-2,6-dimethyloctanal and its use as a fragrance ingredient |
| DE102006021438A1 (de) * | 2006-05-09 | 2007-11-15 | Cognis Ip Management Gmbh | Verfahren zur Ozonolyse von ungesättigten Verbindungen |
| US8754028B2 (en) | 2008-12-16 | 2014-06-17 | The Procter & Gamble Company | Perfume systems |
| DE102009001569A1 (de) * | 2009-03-16 | 2010-09-23 | Henkel Ag & Co. Kgaa | Lilial-Substitut |
| US7842842B1 (en) * | 2009-08-19 | 2010-11-30 | Sami Labs Ltd. | Hydro-alkoxyl citronellal compounds—synthetic routes, compositions and uses thereof |
-
2011
- 2011-10-11 WO PCT/CN2011/080634 patent/WO2013053102A1/en not_active Ceased
-
2012
- 2012-10-11 EP EP12772313.8A patent/EP2766333B1/en active Active
- 2012-10-11 US US14/350,508 patent/US9701606B2/en active Active
- 2012-10-11 ES ES12772313T patent/ES2699775T3/es active Active
- 2012-10-11 MX MX2014004055A patent/MX343612B/es active IP Right Grant
- 2012-10-11 BR BR112014008401A patent/BR112014008401B1/pt active IP Right Grant
- 2012-10-11 JP JP2014535063A patent/JP6343236B2/ja active Active
- 2012-10-11 IN IN2612CHN2014 patent/IN2014CN02612A/en unknown
- 2012-10-11 WO PCT/EP2012/070109 patent/WO2013053787A1/en not_active Ceased
- 2012-10-11 SG SG11201400939YA patent/SG11201400939YA/en unknown
-
2017
- 2017-06-30 JP JP2017128269A patent/JP2017222666A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| MX2014004055A (es) | 2014-05-30 |
| WO2013053102A1 (en) | 2013-04-18 |
| MX343612B (es) | 2016-11-14 |
| JP6343236B2 (ja) | 2018-06-13 |
| WO2013053787A1 (en) | 2013-04-18 |
| BR112014008401A2 (pt) | 2017-04-04 |
| EP2766333A1 (en) | 2014-08-20 |
| JP2017222666A (ja) | 2017-12-21 |
| US9701606B2 (en) | 2017-07-11 |
| EP2766333B1 (en) | 2018-08-29 |
| SG11201400939YA (en) | 2014-07-30 |
| US20140357547A1 (en) | 2014-12-04 |
| IN2014CN02612A (cg-RX-API-DMAC7.html) | 2015-08-07 |
| JP2014528463A (ja) | 2014-10-27 |
| BR112014008401B1 (pt) | 2019-12-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2699775T3 (es) | Procedimiento para la preparación de metoximelonal | |
| CN101990572B (zh) | 羧酸酯作为香味物质的用途 | |
| CN105228993A (zh) | 新型化合物及其作为香料的用途 | |
| EP1398366B1 (en) | Fruity musk compositions | |
| CN110099658B (zh) | 铃兰气味剂 | |
| ES2687171T3 (es) | Compuestos organolépticos | |
| ES2580629T3 (es) | 3-metil-benzofuran-5-ol y su uso en composiciones de perfume | |
| JPH0581639B2 (cg-RX-API-DMAC7.html) | ||
| ES2797925T3 (es) | Nuevos compuestos de octahidroindenil propanal | |
| CN110520513A (zh) | 包含三环[5.2.1.0]-癸烷-8-乙基醚的芳香剂混合物 | |
| ES2595528T3 (es) | 3-(ciclohex-1-en-1-il)propionatos y su uso en composiciones de perfume | |
| ES3042123T3 (en) | A novel furan compound and its use in fragrance formulations | |
| EP1496055B1 (en) | Acetonide fragrance compound | |
| CN103874675B (zh) | 甲氧基甜瓜醛的制备方法 | |
| EP3230257B1 (en) | Enamine and/or aminal fragance precursors derived from (e/z)-9-hydroxy-5,9-dimethyldec-4-enal | |
| EP2902468A2 (en) | Novel cyclopentanol compounds | |
| JP2021532230A (ja) | バラの香りを持つ新規香料 | |
| US10982172B2 (en) | Organoleptic compounds | |
| ES2781089T3 (es) | Composición de fragancia | |
| EP3124478B1 (en) | Novel organoleptic compounds | |
| CN111788172A (zh) | 作为加香成分的环己烯丙醛衍生物 | |
| JP2021504299A (ja) | アンバー調着臭剤 | |
| ES2831311T3 (es) | Compuestos organolépticos novedosos | |
| ES2751901T3 (es) | Compuestos organolépticos noveles | |
| ES2712870T3 (es) | Nuevos compuestos organolépticos |