JP7034441B2 - 香料組成物 - Google Patents
香料組成物 Download PDFInfo
- Publication number
- JP7034441B2 JP7034441B2 JP2018539611A JP2018539611A JP7034441B2 JP 7034441 B2 JP7034441 B2 JP 7034441B2 JP 2018539611 A JP2018539611 A JP 2018539611A JP 2018539611 A JP2018539611 A JP 2018539611A JP 7034441 B2 JP7034441 B2 JP 7034441B2
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- Prior art keywords
- reaction
- carboxylic acid
- mol
- methyl
- formula
- Prior art date
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- 239000003205 fragrance Substances 0.000 title claims description 65
- 239000000203 mixture Substances 0.000 title claims description 52
- 229910052739 hydrogen Inorganic materials 0.000 claims description 34
- 239000001257 hydrogen Substances 0.000 claims description 27
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 24
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
- 239000003814 drug Substances 0.000 claims description 9
- 239000002537 cosmetic Substances 0.000 claims description 6
- 235000013305 food Nutrition 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- 235000013361 beverage Nutrition 0.000 claims description 4
- 229940079593 drug Drugs 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 description 55
- 150000001875 compounds Chemical class 0.000 description 47
- -1 conditioner Substances 0.000 description 37
- 239000003054 catalyst Substances 0.000 description 31
- 239000000047 product Substances 0.000 description 27
- 239000010948 rhodium Substances 0.000 description 19
- 238000007037 hydroformylation reaction Methods 0.000 description 18
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 17
- 150000001336 alkenes Chemical class 0.000 description 17
- 229910002091 carbon monoxide Inorganic materials 0.000 description 17
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 16
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 14
- JESWDXIHOJGWBP-UHFFFAOYSA-N bicyclo[2.2.1]heptane-3-carboxylic acid Chemical compound C1CC2C(C(=O)O)CC1C2 JESWDXIHOJGWBP-UHFFFAOYSA-N 0.000 description 14
- 238000004821 distillation Methods 0.000 description 14
- 238000005984 hydrogenation reaction Methods 0.000 description 14
- 229910052703 rhodium Inorganic materials 0.000 description 14
- 239000007789 gas Substances 0.000 description 13
- 150000002903 organophosphorus compounds Chemical class 0.000 description 13
- 239000002904 solvent Substances 0.000 description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 12
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 12
- OMCJAQLEGLBYJY-UHFFFAOYSA-N bicyclo[2.2.1]hept-2-ene-3-carboxylic acid Chemical compound C1CC2C(C(=O)O)=CC1C2 OMCJAQLEGLBYJY-UHFFFAOYSA-N 0.000 description 11
- 239000002994 raw material Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 10
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 10
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 10
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 10
- 150000002148 esters Chemical class 0.000 description 9
- 238000004817 gas chromatography Methods 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 150000003284 rhodium compounds Chemical class 0.000 description 9
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 8
- 239000003599 detergent Substances 0.000 description 8
- 238000004458 analytical method Methods 0.000 description 7
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 230000002688 persistence Effects 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 238000005698 Diels-Alder reaction Methods 0.000 description 5
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 150000001299 aldehydes Chemical class 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- BWGIKEUGPCOETD-UHFFFAOYSA-N methyl bicyclo[2.2.1]heptane-3-carboxylate Chemical compound C1CC2C(C(=O)OC)CC1C2 BWGIKEUGPCOETD-UHFFFAOYSA-N 0.000 description 5
- 229910052763 palladium Inorganic materials 0.000 description 5
- 229910052697 platinum Inorganic materials 0.000 description 5
- 229910052707 ruthenium Inorganic materials 0.000 description 5
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 4
- 239000002304 perfume Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 238000001308 synthesis method Methods 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- GGRQQHADVSXBQN-FGSKAQBVSA-N carbon monoxide;(z)-4-hydroxypent-3-en-2-one;rhodium Chemical compound [Rh].[O+]#[C-].[O+]#[C-].C\C(O)=C\C(C)=O GGRQQHADVSXBQN-FGSKAQBVSA-N 0.000 description 3
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 3
- 230000006698 induction Effects 0.000 description 3
- 238000010813 internal standard method Methods 0.000 description 3
- 229910052987 metal hydride Inorganic materials 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 239000011949 solid catalyst Substances 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- GEWDNTWNSAZUDX-WQMVXFAESA-N (-)-methyl jasmonate Chemical compound CC\C=C/C[C@@H]1[C@@H](CC(=O)OC)CCC1=O GEWDNTWNSAZUDX-WQMVXFAESA-N 0.000 description 2
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
- CRDAMVZIKSXKFV-YFVJMOTDSA-N (2-trans,6-trans)-farnesol Chemical compound CC(C)=CCC\C(C)=C\CC\C(C)=C\CO CRDAMVZIKSXKFV-YFVJMOTDSA-N 0.000 description 2
- 0 **C(*)(C1C=CC2C1)C2(*)O Chemical compound **C(*)(C1C=CC2C1)C2(*)O 0.000 description 2
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- LOKPJYNMYCVCRM-UHFFFAOYSA-N 16-Hexadecanolide Chemical compound O=C1CCCCCCCCCCCCCCCO1 LOKPJYNMYCVCRM-UHFFFAOYSA-N 0.000 description 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- OALYTRUKMRCXNH-UHFFFAOYSA-N 5-pentyloxolan-2-one Chemical compound CCCCCC1CCC(=O)O1 OALYTRUKMRCXNH-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 2
- DZNVIZQPWLDQHI-UHFFFAOYSA-N Citronellyl formate Chemical compound O=COCCC(C)CCC=C(C)C DZNVIZQPWLDQHI-UHFFFAOYSA-N 0.000 description 2
- 244000241257 Cucumis melo Species 0.000 description 2
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- 240000001972 Gardenia jasminoides Species 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 235000010254 Jasminum officinale Nutrition 0.000 description 2
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- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
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- 241000581835 Monodora junodii Species 0.000 description 2
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- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
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- 235000009508 confectionery Nutrition 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- OSOIQJGOYGSIMF-UHFFFAOYSA-N cyclopentadecanone Chemical compound O=C1CCCCCCCCCCCCCC1 OSOIQJGOYGSIMF-UHFFFAOYSA-N 0.000 description 2
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 2
- 239000000645 desinfectant Substances 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 229910052741 iridium Inorganic materials 0.000 description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
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- 239000006210 lotion Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
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- GEWDNTWNSAZUDX-UHFFFAOYSA-N methyl 7-epi-jasmonate Natural products CCC=CCC1C(CC(=O)OC)CCC1=O GEWDNTWNSAZUDX-UHFFFAOYSA-N 0.000 description 2
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 2
- 229940095102 methyl benzoate Drugs 0.000 description 2
- KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 description 2
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 description 2
- 229910052762 osmium Inorganic materials 0.000 description 2
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- SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
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- 239000000377 silicon dioxide Substances 0.000 description 2
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- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 2
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- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- IFDFMWBBLAUYIW-UHFFFAOYSA-N ethane-1,2-diol;ethyl acetate Chemical compound OCCO.CCOC(C)=O IFDFMWBBLAUYIW-UHFFFAOYSA-N 0.000 description 1
- PZUDDXJZNSJESK-UHFFFAOYSA-N ethyl 2-cyclohexylpropanoate Chemical compound CCOC(=O)C(C)C1CCCCC1 PZUDDXJZNSJESK-UHFFFAOYSA-N 0.000 description 1
- UTXVCHVLDOLVPC-UHFFFAOYSA-N ethyl 3-methylbut-2-enoate Chemical compound CCOC(=O)C=C(C)C UTXVCHVLDOLVPC-UHFFFAOYSA-N 0.000 description 1
- 229940093499 ethyl acetate Drugs 0.000 description 1
- 235000019439 ethyl acetate Nutrition 0.000 description 1
- CIHQTYMOCREEQU-UHFFFAOYSA-N ethyl bicyclo[2.2.1]heptane-3-carboxylate Chemical compound C1CC2C(C(=O)OCC)CC1C2 CIHQTYMOCREEQU-UHFFFAOYSA-N 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229930002886 farnesol Natural products 0.000 description 1
- 229940043259 farnesol Drugs 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000019253 formic acid Nutrition 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
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
- 229940020436 gamma-undecalactone Drugs 0.000 description 1
- 239000000499 gel Substances 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
- 229940113087 geraniol Drugs 0.000 description 1
- FQMZVFJYMPNUCT-UHFFFAOYSA-N geraniol formate Natural products CC(C)=CCCC(C)=CCOC=O FQMZVFJYMPNUCT-UHFFFAOYSA-N 0.000 description 1
- 235000008397 ginger Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- UFLHIIWVXFIJGU-UHFFFAOYSA-N hex-3-en-1-ol Natural products CCC=CCCO UFLHIIWVXFIJGU-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 230000003100 immobilizing effect Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000001102 lavandula vera Substances 0.000 description 1
- 235000018219 lavender Nutrition 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 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
- 239000000395 magnesium oxide Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229940126601 medicinal product Drugs 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 1
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- MCVVUJPXSBQTRZ-ONEGZZNKSA-N methyl (e)-but-2-enoate Chemical compound COC(=O)\C=C\C MCVVUJPXSBQTRZ-ONEGZZNKSA-N 0.000 description 1
- NRDTWOHSERCKMQ-UHFFFAOYSA-N methyl 1-formylbicyclo[2.2.1]heptane-2-carboxylate Chemical compound COC(=O)C1C2(CCC(C1)C2)C=O NRDTWOHSERCKMQ-UHFFFAOYSA-N 0.000 description 1
- ZWNPUELCBZVMDA-HJWRWDBZSA-N methyl 2-nonenoate Chemical compound CCCCCC\C=C/C(=O)OC ZWNPUELCBZVMDA-HJWRWDBZSA-N 0.000 description 1
- FZIBCCGGICGWBP-UHFFFAOYSA-N methyl 3-methylbut-2-enoate Chemical compound COC(=O)C=C(C)C FZIBCCGGICGWBP-UHFFFAOYSA-N 0.000 description 1
- ZEZRPJIPNVBIEE-UHFFFAOYSA-N methyl 5-formylbicyclo[2.2.1]heptane-3-carboxylate Chemical compound C1C(C=O)C2C(C(=O)OC)CC1C2 ZEZRPJIPNVBIEE-UHFFFAOYSA-N 0.000 description 1
- 229940102398 methyl anthranilate Drugs 0.000 description 1
- 229960001047 methyl salicylate Drugs 0.000 description 1
- JPTOCTSNXXKSSN-UHFFFAOYSA-N methylheptenone Chemical compound CCCC=CC(=O)CC JPTOCTSNXXKSSN-UHFFFAOYSA-N 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 235000011929 mousse Nutrition 0.000 description 1
- 239000002324 mouth wash Substances 0.000 description 1
- 229940051866 mouthwash Drugs 0.000 description 1
- FALTVGCCGMDSNZ-UHFFFAOYSA-N n-(1-phenylethyl)benzamide Chemical compound C=1C=CC=CC=1C(C)NC(=O)C1=CC=CC=C1 FALTVGCCGMDSNZ-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229940094933 n-dodecane Drugs 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- WASNIKZYIWZQIP-AWEZNQCLSA-N nerolidol Natural products CC(=CCCC(=CCC[C@@H](O)C=C)C)C WASNIKZYIWZQIP-AWEZNQCLSA-N 0.000 description 1
- HIGQPQRQIQDZMP-FLIBITNWSA-N neryl acetate Chemical compound CC(C)=CCC\C(C)=C/COC(C)=O HIGQPQRQIQDZMP-FLIBITNWSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 1
- UMRZSTCPUPJPOJ-KNVOCYPGSA-N norbornane Chemical group C1C[C@H]2CC[C@@H]1C2 UMRZSTCPUPJPOJ-KNVOCYPGSA-N 0.000 description 1
- 239000001702 nutmeg Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 150000002989 phenols Chemical class 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
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 229940081310 piperonal Drugs 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 229930007790 rose oxide Natural products 0.000 description 1
- 235000002020 sage Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 235000015961 tonic Nutrition 0.000 description 1
- 230000001256 tonic effect Effects 0.000 description 1
- 229960000716 tonics Drugs 0.000 description 1
- 229940034610 toothpaste Drugs 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- NPFVOOAXDOBMCE-UHFFFAOYSA-N trans-3-hexenyl acetate Natural products CCC=CCCOC(C)=O NPFVOOAXDOBMCE-UHFFFAOYSA-N 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
- XMLSXPIVAXONDL-UHFFFAOYSA-N trans-jasmone Natural products CCC=CCC1=C(C)CCC1=O XMLSXPIVAXONDL-UHFFFAOYSA-N 0.000 description 1
- ZFDIRQKJPRINOQ-UHFFFAOYSA-N transbutenic acid ethyl ester Natural products CCOC(=O)C=CC ZFDIRQKJPRINOQ-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
- UAXOELSVPTZZQG-UHFFFAOYSA-N trimethyl acrylic acid Chemical compound CC(C)=C(C)C(O)=O UAXOELSVPTZZQG-UHFFFAOYSA-N 0.000 description 1
- KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- 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
-
- 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
- C11B9/0038—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing more 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 COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
- A23L2/56—Flavouring or bittering agents
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- 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 COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/20—Synthetic spices, flavouring agents or condiments
- A23L27/203—Alicyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/14—Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
-
- 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
- C07C69/753—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring of polycyclic acids
-
- 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
- C07C69/757—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/96—Esters of carbonic or haloformic 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
-
- 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
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/36—Systems containing two condensed rings the rings having more than two atoms in common
- C07C2602/42—Systems containing two condensed rings the rings having more than two atoms in common the bicyclo ring system containing seven carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Nutrition Science (AREA)
- Wood Science & Technology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Fats And Perfumes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cosmetics (AREA)
- Seasonings (AREA)
- Non-Alcoholic Beverages (AREA)
- Detergent Compositions (AREA)
Description
[1]
式(1)で表される化合物;
Xは、炭素数1~4のアルキル基であり、
R4及びR5は、独立して、水素、又は-CHO基であり、
を含有する、香料組成物。
[2]
式(1)で表される化合物が、以下の式(1-1)~式(1-3);
Xは、炭素数1~4のアルキル基である。)
Xは、炭素数1~4のアルキル基である。)
Xは、炭素数1~4のアルキル基であり、
R4及びR5のいずれか一方は、水素であり、もう一方は、-CHO基である。)
からなる群より選択される1種以上である、[1]に記載の香料組成物。
[3]
[1]又は[2]に記載の香料組成物を含有する、香粧品、健康衛生材料、雑貨、飲料、食品、医薬部外品又は医薬品。
本実施形態の香料組成物は、ノルボルナン-2-カルボン酸エステル化合物類、すなわち、式(1)で表される化合物を含有する。
本実施形態の香料組成物とは、式(1)で表される化合物単独又は2種以上を主成分とする香料組成物であってもよく、通常用いられる他の香料成分や、所望組成の調合香料に、式(1)で表される化合物を単独で又は2種以上を混合した香料組成物であってもよい。
式(1)で表される化合物単独又は2種以上を主成分とするとは、式(1)で表される化合物を、該香料組成物全量に対し通常85質量%以上、好ましくは90質量%以上、より好ましくは96質量%以上、さらに好ましくは98質量%以上含むことを指す。
すなわち、R1 、R2 、R3は、独立して、水素又はメチル基であり、
Xは、炭素数1~4のアルキル基である。
すなわち、R1 、R2 、R3は、独立して、水素又はメチル基であり、
Xは、炭素数1~4のアルキル基である。
すなわち、式(1-3)中、R1 、R2 、R3は、独立して、水素又はメチル基であり、
Xは、炭素数1~4のアルキル基である。
R4及びR5のいずれか一方は、水素であり、もう一方は、-CHO基である。
R2及びR3は、好ましくは水素である。
また、式(1)、式(1-1)~式(1-3)におけるXは、炭素数1~4のアルキル基である。炭素数1~4のアルキル基としては、メチル基、エチル基、n-プロピル基、iso-プロピル基、n-ブチル基、iso-ブチル基、tert-ブチル基が挙げられる。Xは、好ましくはメチル基及びエチル基である。
本実施形態における式(1-1)で表される化合物は、強い完熟バナナとメロン様のフルーティさと、オゾン様のマリンノートを合わせ持つ香気、ないしはフレッシュなフローラルグリーン調の香りとフルーティさを合わせ持った香気を有し、かつ持続性にも優れる。
本実施形態における式(1-2)で表される化合物は、フルーティ感のあるハーバルグリーン様の香気を有し、かつ持続性にも優れる。
本実施形態における式(1-3)で表される化合物は、強いメロンやキウイ様フルーティさとフレッシュなマリンノート、及びローズ様フローラルを合わせ持つ新規な香気であり、かつ持続性にも優れる。
本実施形態における式(1)で表される化合物は、例えば、オレフィンとジシクロペンタジエンとを加熱反応するディールス-アルダー反応を鍵工程とする合成法により製造することができる。
具体的には、式(1-1)で表される化合物は、以下のとおりオレフィンとジシクロペンタジエンとを加熱反応するディールス-アルダー反応により製造することができる。
一方、高沸物質の副生を抑えるために、反応温度は、好ましくは250℃以下の温度である。
また、反応溶媒として炭化水素類やアルコール類、エステル類等を使用することも可能であり、炭素数6以上の脂肪族炭化水素類、具体的には、シクロヘキサン、トルエン、キシレン、エチルベンゼン、メシチレン、プロパノール、ブタノール等が好適である。
得られた生成物、すなわち、式(1-1)で表される化合物は、次の反応の原料とすることができ、式(1-2)で表される化合物及び式(1-3)で表される化合物を合成するための原料とすることができる。
担持金属触媒としては、具体的には、銅-クロム触媒(Adkins触媒)、銅-亜鉛触媒、銅-鉄等の銅触媒を担体に担持した担持銅触媒、Pt/CやPt/アルミナ等の担持白金触媒、Pd/CやPd/アルミナ等の担持パラジウム触媒、Ru/CやRu/アルミナ等の担持ルテニウム触媒、Rh/CやRh/アルミナ等の担持ロジウム触媒等が好適に挙げられる。
これらの触媒の中でも、反応活性及び選択性の点で、より好ましくは銅を含有する触媒である。
溶媒としては、水、ギ酸、及び酢酸等の有機酸類;酢酸エチル、及び酢酸ブチル等のエステル類;ベンゼン、o-ジクロロベンゼン、トルエン、及びキシレン等の芳香族化合物類;ヘキサン、ヘプタン、及びシクロヘキサン等の炭化水素類;メタノール、エタノール、イソプロピルアルコール、t-ブチルアルコール、エチレングリコール、及びジエチレングリコール等のアルコール類;ジオキサン、テトラヒドロフラン、ジメトキシエタン、及びジグライム等のエーテル類;等、あるいはこれらの混合物が挙げられる。
水素化反応で溶媒を使用する際の溶媒の量は、原料であるノルボルネン-2-カルボン酸エステル化合物に対し、通常0.1~30質量倍であり、好ましくは0.2~20質量倍である。
R6、R7、R8の具体例としては、炭素数1~4のアルキル基又は炭素数1~4のアルコキシ基で置換されていてもよいアリール基、及び炭素数1~4のアルキル基又は炭素数1~4のアルコキシ基で置換されていてもよい脂環式アルキル基等が挙げられる。
有機リン化合物としては、具体的には、トリフェニルホスフィン、トリフェニルホスファイトが好適に用いられる。
有機リン化合物の使用量は、好ましくはロジウム金属の500倍モル~10000倍モルであり、より好ましくは700倍モル~5000倍モルであり、さらに好ましくは900倍モル~2000倍モルである。有機リン化合物の使用量がロジウム金属の500倍モルよりも少ない場合、触媒活物質のロジウム金属ヒドリドカルボニルリン錯体の安定性が損なわれ、反応の進行が遅くなる傾向にある。また、有機リン化合物の使用量がロジウム金属の10000倍モルよりも多い場合、有機リン化合物に掛かるコストが増える傾向にある。
溶媒としては、具体的には、脂肪族炭化水素、脂環式炭化水素、及び芳香族炭化水素等の炭化水素類;脂肪族エステル、脂環式エステル、及び芳香族エステル等のエステル類;脂肪族アルコール、及び脂環式アルコール等のアルコール類;芳香族ハロゲン化物;等が挙げられる。これらの溶媒の中でも、好ましくは炭化水素類であり、より好ましくは脂環式炭化水素、芳香族炭化水素である。
式(1)で表わされる化合物を含有する香料組成物は、例えば、香水、コロン類等のフレグランス製品;シャンプー、リンス類、ヘアートニック、ヘアークリーム類、ムース、ジェル、ポマード、スプレーその他毛髪用化粧料;化粧水、美容液、クリーム、乳液、パック、ファンデーション、おしろい、口紅、各種メークアップ類等の肌用化粧料;皿洗い洗剤、洗濯用洗剤、ソフトナー類、消毒用洗剤類、消臭洗剤類、室内芳香剤、ファーニチアケアー、ガラスクリーナー、家具クリーナー、床クリーナー、消毒剤、殺虫剤、漂白剤、その他の各種健康衛生用洗剤類;歯磨、マウスウォッシュ、入浴剤、制汗製品、パーマ液等の医薬部外品;トイレットペーパー、ティッシュペーパー等の雑貨;医薬品等;食品等の香気成分として使用することができる。
<ガスクロマトグラフィー分析条件>
・分析装置 :株式会社島津製作所製 キャピラリガスクロマトグラフGC-2010 Plus
・分析カラム :ジーエルサイエンス株式会社製、InertCap1(30m、0.32mmI.D.、膜厚0.25μm
・オーブン温度:60℃(0.5分間)-昇温速度15℃/分-280℃(4分間)
・検出器 :FID、温度280℃
ガスクロマトグラフィー分析により、生成物であるカルボン酸エステル化合物の面積割合(GC%)を求め、内部標準法によりノルボルネン-2-カルボン酸エステル、及びノルボルナン-2-カルボン酸エステル化合物の収率、選択率を下記式により算出した。
・オレフィン基準の収率(モル%)=ノルボルネン-2-カルボン酸エステルの取得量(モル)/オレフィンの仕込み量(モル)×100
・ジシクロペンタジエン基準の収率(モル%)=ノルボルネン-2-カルボン酸エステルの取得量(モル)/ジシクロペンタジエンの仕込み量(モル)×100/2
・オレフィン基準の選択率(モル%)=ノルボルネン-2-カルボン酸エステルの取得量(モル)/オレフィンの反応量(モル)×100
・ジシクロペンタジエン基準の選択率(モル%)=ノルボルネン-2-カルボン酸エステルの取得量(モル)/ジシクロペンタジエンの反応量(モル)×100/2
・水素化反応の収率(モル%)=ノルボルナン-2-カルボン酸エステルの取得量(モル)/(ノルボルネン-2-カルボン酸エステルの仕込み量(モル)×100
・水素化反応の選択率(モル%)=ノルボルナン-2-カルボン酸エステルの取得量(モル)/ノルボルネン-2-カルボン酸エステルの反応量(モル)×100
・ヒドロホルミル化反応の収率(モル%)=ホルミルノルボルナン-2-カルボン酸エステルの取得量(モル)/ノルボルネン-2-カルボン酸エステルの仕込み量(モル)×100
・ヒドロホルミル化反応の選択率(モル%)=ホルミルノルボルナン-2-カルボン酸エステルの取得量(モル)/ノルボルネン-2-カルボン酸エステルの反応量(モル)×100
・分析装置 :株式会社島津製作所製、GCMS-QP2010 Plus
・イオン化電圧:70eV
・分析カラム :Agilent Technologies製、DB-1(30m、0.32mmI.D.、膜厚1.00μm)
・オーブン温度:60℃(0.5分間)-昇温速度15℃/分-280℃(4分間)
(ノルボルネン-2-カルボン酸メチルエステルの合成法)
まず、オートクレーブにn-ドデカン(東京化成製試薬特級)101.2g仕込み、窒素ガス置換後、液温195℃とした。
反応温度を195℃に保持しながら、アクリル酸メチル96.4g(1.12モル)とジシクロペンタジエン105.7g(0.80モル)の混合液をオートクレーブ上部より1時間かけて供給した後、更に、2時間攪拌を継続した。
得られた液を理論段数20段の精留塔を用いて精留を行ったところ(留出温度88℃、真空度2.7kPa)、主留部分としてガスクロマトグラフィー分析で98.5GC%のものが120.5g(蒸留収率90.5モル%)で得られた。
得られた留分をGC-MSで分析した結果、目的物の分子量152を示した。
まず、表1に示す組成の香料組成物(コントロール品)を作製した。次に、このコントロール品90質量部に上記で調製したノルボルネン-2-カルボン酸メチルエステル10質量部を加えて香料組成物を作製した。
得られた香料組成物は、調香師による香り評価において、華やかなガーデニア様フローラル感を有するアプリコット様フルーティの香りであることが確認された。
(ノルボルネン-2-メチル-2-カルボン酸メチルエステルの合成法)
前記反応液を冷却後、得られた液316.9gを内部標準法によりガスクロマトグラフィーで分析した結果、目的のノルボルネン-2-メチル-2-カルボン酸メチルエステル化合物140.0gが含有されていた。メタクリル酸メチル基準の成績は収率75.2モル%、選択率75.9モル%であり、ジシクロペンタジエン基準の成績は収率52.7モル%、選択率57.4モル%であった。
得られた液を理論段数40段の回転バンド蒸留塔を用いて精留を行ったところ(留出温度90℃、真空度2.7kPa)、主留部分としてガスクロマトグラフィー分析で98.5GC%のものが127.5g(蒸留収率91.1モル%)で得られた。
得られた留分をGC-MSで分析した結果、目的物の分子量166を示した。
まず、表2に示す組成の香料組成物(コントロール品)を作製した。次に、このコントロール品90質量部に上記で調製したノルボルネン-2-メチル-2-カルボン酸メチルエステル10質量部を加えて香料組成物を作製した。
得られた香料組成物は、調香師による香り評価において、瑞々しい洋ナシを思わせる様なフルーツタイプの香りであることが確認された。
(ノルボルナン-2-カルボン酸メチルエステルの合成法)
前記オートクレーブに、Cu-Cr触媒(日揮製N-203S)を6.0g、イソプロピルアルコール(和光純薬工業製特級)を120.0g仕込み、170℃、水素圧2MPa下で1時間の活性化を行った。冷却後、上記で調製したノルボルネン-2-カルボン酸メチルエステルを60.0g仕込み、120℃、水素圧2MPa、3時間攪拌して還元反応を行った。反応液を濾過して触媒を除き、ノルボルナン-2-カルボン酸メチルエステル57.6gを含有する反応液173.9g得た(転化率100%、収率96.2%)。ノルボルネン-2-カルボン酸メチルエステル基準の成績は収率96.2モル%、選択率100モル%であった。
得られた留分をGC-MSで分析した結果、目的物の分子量154を示した。
まず、表3に示す組成の香料組成物(コントロール品)を作製した。次に、このコントロール品90質量部に上記で調製したノルボルナン-2-カルボン酸メチルエステル10質量部を加えて香料組成物を作製した。
得られた香料組成物は、調香師による香り評価において、青リンゴのフレッシュ感を持つフルーツタイプの香りであることが確認された。
(ホルミルノルボルナン-2-カルボン酸メチルエステルの合成法)
前記オートクレーブに、上記で調製したノルボルネン-2-カルボン酸メチルエステルを60.0g、トルエン116.9g、亜リン酸トリフェニル0.37g、別途調製したRh(acac)(CO)2のトルエン溶液3.10g(濃度0.01wt%)を加えた。窒素及びCO/H2混合ガスによる置換を各々3回行った後、CO/H2混合ガスで系内を加圧し、100℃、2MPaにて5時間反応を行った。反応終了後、反応液のガスクロマトグラフィー分析を行い、ホルミルノルボルナン-2-カルボン酸メチルエステル(5-ホルミルノルボルナン-2-カルボン酸メチルエステル及び6-ホルミルノルボルナン-2-カルボン酸メチルエステルの混合物)69.0gを含有する反応液186.9g得た。ノルボルネン-2-カルボン酸メチルエステル基準の成績は収率96.2モル%、選択率100モル%であった。
得られた留分をGC-MSで分析した結果、目的物の分子量182を示した。
まず、表4に示す組成の香料組成物(コントロール品)を作製した。次に、このコントロール品90質量部に上記で調製したホルミルノルボルナン-2-カルボン酸メチルエステル10質量部を加えて香料組成物を作製した。
得られた香料組成物は、調香師による香り評価において、甘く華やかなガーデニアを思わせるフローラル感を持つフルーツタイプの香りであることが確認された。
Claims (3)
- (削除)
- 請求項2に記載の香料組成物を含有する、香粧品、健康衛生材料、雑貨、飲料、食品、医薬部外品又は医薬品。
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- 2017-08-28 CN CN201780057025.7A patent/CN109715771A/zh active Pending
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WO2015146876A1 (ja) | 2014-03-27 | 2015-10-01 | Kjケミカルズ株式会社 | グリシジル基含有(メタ)アクリルアミド |
Non-Patent Citations (1)
Title |
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PODLEJSKI, J. et al.,Synthesis of odoriferous compounds by Diels-Alder reaction,Pollena: Tluszcze, Srodki Piorace, Kosmetyki,(1986), vol.30, No.5-8,pp.166-169,CAplus [online], US: American Chemical Society,[retrieved on 2021.08.12], Retrieved from: STN, Accession No.1987:195935 |
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EP3514221A4 (en) | 2019-08-07 |
US20200283696A1 (en) | 2020-09-10 |
US11098267B2 (en) | 2021-08-24 |
US20190241833A1 (en) | 2019-08-08 |
KR102522953B1 (ko) | 2023-04-18 |
WO2018051776A1 (ja) | 2018-03-22 |
EP3514221B1 (en) | 2022-01-19 |
EP3514221A1 (en) | 2019-07-24 |
JPWO2018051776A1 (ja) | 2019-06-27 |
CN109715771A (zh) | 2019-05-03 |
KR20190054070A (ko) | 2019-05-21 |
ES2907783T3 (es) | 2022-04-26 |
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