JPWO2019194186A1 - ムスク様組成物 - Google Patents
ムスク様組成物 Download PDFInfo
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- JPWO2019194186A1 JPWO2019194186A1 JP2020512264A JP2020512264A JPWO2019194186A1 JP WO2019194186 A1 JPWO2019194186 A1 JP WO2019194186A1 JP 2020512264 A JP2020512264 A JP 2020512264A JP 2020512264 A JP2020512264 A JP 2020512264A JP WO2019194186 A1 JPWO2019194186 A1 JP WO2019194186A1
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- Prior art keywords
- fragrance
- general formula
- compound represented
- composition
- composition according
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 113
- 239000003205 fragrance Substances 0.000 claims abstract description 113
- 150000001875 compounds Chemical class 0.000 claims abstract description 99
- 239000002304 perfume Substances 0.000 claims description 27
- 241000402754 Erythranthe moschata Species 0.000 claims description 24
- 239000012459 cleaning agent Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 19
- 239000003795 chemical substances by application Substances 0.000 claims description 18
- 150000002148 esters Chemical class 0.000 claims description 15
- 150000001298 alcohols Chemical class 0.000 claims description 13
- 239000002537 cosmetic Substances 0.000 claims description 11
- 150000002170 ethers Chemical class 0.000 claims description 9
- 150000001299 aldehydes Chemical class 0.000 claims description 7
- 239000000835 fiber Substances 0.000 claims description 7
- 150000001735 carboxylic acids Chemical class 0.000 claims description 6
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 5
- 239000000284 extract Substances 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 150000002576 ketones Chemical class 0.000 claims description 5
- 150000002596 lactones Chemical class 0.000 claims description 5
- 239000000341 volatile oil Substances 0.000 claims description 5
- 150000001241 acetals Chemical class 0.000 claims description 4
- 150000002825 nitriles Chemical class 0.000 claims description 4
- 150000002989 phenols Chemical class 0.000 claims description 4
- 230000002708 enhancing effect Effects 0.000 claims description 2
- 230000000694 effects Effects 0.000 abstract description 13
- 239000000126 substance Substances 0.000 abstract description 4
- -1 aliphatic alcohols Chemical class 0.000 description 35
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- 238000004519 manufacturing process Methods 0.000 description 18
- 230000000052 comparative effect Effects 0.000 description 16
- KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 description 16
- 239000003921 oil Substances 0.000 description 15
- 235000019198 oils Nutrition 0.000 description 15
- 238000002156 mixing Methods 0.000 description 11
- ALHUZKCOMYUFRB-UHFFFAOYSA-N muskone Natural products CC1CCCCCCCCCCCCC(=O)C1 ALHUZKCOMYUFRB-UHFFFAOYSA-N 0.000 description 9
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- GPVOTKFXWGURGP-UHFFFAOYSA-N 2,5,5-trimethyl-1,3,4,4a,6,7-hexahydronaphthalen-2-ol Chemical compound C1C(C)(O)CCC2C1=CCCC2(C)C GPVOTKFXWGURGP-UHFFFAOYSA-N 0.000 description 7
- ALHUZKCOMYUFRB-OAHLLOKOSA-N Muscone Chemical compound C[C@@H]1CCCCCCCCCCCCC(=O)C1 ALHUZKCOMYUFRB-OAHLLOKOSA-N 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
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- 229940022663 acetate Drugs 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 238000005649 metathesis reaction Methods 0.000 description 6
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- 238000006243 chemical reaction Methods 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
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- YPZUZOLGGMJZJO-UHFFFAOYSA-N Ambronide Chemical compound C1CC2C(C)(C)CCCC2(C)C2C1(C)OCC2 YPZUZOLGGMJZJO-UHFFFAOYSA-N 0.000 description 4
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 4
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- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- JIYIHILAGIZIMD-CLFYSBASSA-N (4z)-cyclopentadec-4-en-1-one Chemical compound O=C1CCCCCCCCCC\C=C/CC1 JIYIHILAGIZIMD-CLFYSBASSA-N 0.000 description 3
- WUOACPNHFRMFPN-SECBINFHSA-N (S)-(-)-alpha-terpineol Chemical compound CC1=CC[C@@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-SECBINFHSA-N 0.000 description 3
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 3
- WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 3
- 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 3
- PUKWIVZFEZFVAT-UHFFFAOYSA-N 2,2,5-trimethyl-5-pentylcyclopentan-1-one Chemical compound CCCCCC1(C)CCC(C)(C)C1=O PUKWIVZFEZFVAT-UHFFFAOYSA-N 0.000 description 3
- NVIPUOMWGQAOIT-DUXPYHPUSA-N 7-hexadecen-1,16-olide Chemical compound O=C1CCCCC\C=C\CCCCCCCCO1 NVIPUOMWGQAOIT-DUXPYHPUSA-N 0.000 description 3
- 239000005711 Benzoic acid Substances 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 241000220317 Rosa Species 0.000 description 3
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 3
- OVKDFILSBMEKLT-UHFFFAOYSA-N alpha-Terpineol Natural products CC(=C)C1(O)CCC(C)=CC1 OVKDFILSBMEKLT-UHFFFAOYSA-N 0.000 description 3
- 229940088601 alpha-terpineol Drugs 0.000 description 3
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 3
- 235000010233 benzoic acid Nutrition 0.000 description 3
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 229930016911 cinnamic acid Natural products 0.000 description 3
- 235000013985 cinnamic acid Nutrition 0.000 description 3
- ABRIMXGLNHCLIP-UHFFFAOYSA-N cyclohexadec-5-en-1-one Chemical compound O=C1CCCCCCCCCCC=CCCC1 ABRIMXGLNHCLIP-UHFFFAOYSA-N 0.000 description 3
- SFHGCJOKUVVNIE-UHFFFAOYSA-N dec-9-enyl oct-7-enoate Chemical compound C=CCCCCCCCCOC(=O)CCCCCC=C SFHGCJOKUVVNIE-UHFFFAOYSA-N 0.000 description 3
- 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 3
- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 description 3
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 3
- 239000000344 soap 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
- YPZUZOLGGMJZJO-XRGAULLZSA-N (3as,5as,9as,9br)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1h-benzo[e][1]benzofuran Chemical compound CC([C@@H]1CC2)(C)CCC[C@]1(C)[C@@H]1[C@@]2(C)OCC1 YPZUZOLGGMJZJO-XRGAULLZSA-N 0.000 description 2
- ZGEHHVDYDNXYMW-OWOJBTEDSA-N (8e)-cyclohexadec-8-en-1-one Chemical compound O=C1CCCCCCC\C=C\CCCCCC1 ZGEHHVDYDNXYMW-OWOJBTEDSA-N 0.000 description 2
- JRJBVWJSTHECJK-LUAWRHEFSA-N (z)-3-methyl-4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one Chemical compound CC(=O)C(\C)=C/C1C(C)=CCCC1(C)C JRJBVWJSTHECJK-LUAWRHEFSA-N 0.000 description 2
- GQBVHGLNSHPKPG-UHFFFAOYSA-N 1-(2-tert-butylcyclohexyl)oxybutan-2-ol Chemical compound CCC(O)COC1CCCCC1C(C)(C)C GQBVHGLNSHPKPG-UHFFFAOYSA-N 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N 1-nonene Chemical compound CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- LOKPJYNMYCVCRM-UHFFFAOYSA-N 16-Hexadecanolide Chemical compound O=C1CCCCCCCCCCCCCCCO1 LOKPJYNMYCVCRM-UHFFFAOYSA-N 0.000 description 2
- GNVAISZHADZKJR-UHFFFAOYSA-N 2,2,4-trimethyl-1-(2-methylprop-2-enoxy)pentan-3-ol Chemical compound CC(C)C(O)C(C)(C)COCC(C)=C GNVAISZHADZKJR-UHFFFAOYSA-N 0.000 description 2
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 2
- UJVMVSBNTJTGOO-UHFFFAOYSA-N 3-chloro-n-(5-fluoro-2-methylphenyl)propanamide Chemical compound CC1=CC=C(F)C=C1NC(=O)CCCl UJVMVSBNTJTGOO-UHFFFAOYSA-N 0.000 description 2
- GVPGXFIINYYZAR-UHFFFAOYSA-N 3-methylcyclopentadecan-1-ol Chemical compound CC1CCCCCCCCCCCCC(O)C1 GVPGXFIINYYZAR-UHFFFAOYSA-N 0.000 description 2
- RHLVCLIPMVJYKS-UHFFFAOYSA-N 3-octanone Chemical compound CCCCCC(=O)CC RHLVCLIPMVJYKS-UHFFFAOYSA-N 0.000 description 2
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- 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 2
- OALYTRUKMRCXNH-UHFFFAOYSA-N 5-pentyloxolan-2-one Chemical compound CCCCCC1CCC(=O)O1 OALYTRUKMRCXNH-UHFFFAOYSA-N 0.000 description 2
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- SYOSSKZMWMHVSA-UHFFFAOYSA-N 8,8-bis(1h-indol-3-yl)-2,6-dimethyloctan-2-ol Chemical compound C1=CC=C2C(C(C=3C4=CC=CC=C4NC=3)CC(CCCC(C)(C)O)C)=CNC2=C1 SYOSSKZMWMHVSA-UHFFFAOYSA-N 0.000 description 2
- SCCDQYPEOIRVGX-UHFFFAOYSA-N Acetyleugenol Chemical compound COC1=CC(CC=C)=CC=C1OC(C)=O SCCDQYPEOIRVGX-UHFFFAOYSA-N 0.000 description 2
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- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- GVPGXFIINYYZAR-OEMAIJDKSA-N CC(CCCCCCCCCCCC1)C[C@@H]1O Chemical compound CC(CCCCCCCCCCCC1)C[C@@H]1O GVPGXFIINYYZAR-OEMAIJDKSA-N 0.000 description 2
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-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
- 244000004281 Eucalyptus maculata Species 0.000 description 2
- 241000208152 Geranium Species 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
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- 239000002262 Schiff base Substances 0.000 description 2
- 150000004753 Schiff bases Chemical class 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- KGEKLUUHTZCSIP-HOSYDEDBSA-N [(1s,4s,6r)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] acetate Chemical compound C1C[C@]2(C)[C@H](OC(=O)C)C[C@H]1C2(C)C KGEKLUUHTZCSIP-HOSYDEDBSA-N 0.000 description 2
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- 239000002253 acid Substances 0.000 description 2
- IGODOXYLBBXFDW-UHFFFAOYSA-N alpha-Terpinyl acetate Chemical compound CC(=O)OC(C)(C)C1CCC(C)=CC1 IGODOXYLBBXFDW-UHFFFAOYSA-N 0.000 description 2
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- 239000002585 base Substances 0.000 description 2
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- NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 description 2
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
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- 238000004817 gas chromatography Methods 0.000 description 2
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- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
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- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- GEWDNTWNSAZUDX-UHFFFAOYSA-N methyl 7-epi-jasmonate Natural products CCC=CCC1C(CC(=O)OC)CCC1=O GEWDNTWNSAZUDX-UHFFFAOYSA-N 0.000 description 2
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- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
- NJGBTKGETPDVIK-UHFFFAOYSA-N raspberry ketone Chemical compound CC(=O)CCC1=CC=C(O)C=C1 NJGBTKGETPDVIK-UHFFFAOYSA-N 0.000 description 1
- 229930007790 rose oxide Natural products 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 235000002020 sage Nutrition 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 0.000 description 1
- 230000009291 secondary effect Effects 0.000 description 1
- 230000014860 sensory perception of taste Effects 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 238000010183 spectrum analysis Methods 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 229930006978 terpinene Natural products 0.000 description 1
- 150000003507 terpinene derivatives Chemical class 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- YUVKTUCPWGPBLJ-UHFFFAOYSA-N tert-butyl 2-cyclohexylacetate Chemical compound CC(C)(C)OC(=O)CC1CCCCC1 YUVKTUCPWGPBLJ-UHFFFAOYSA-N 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- UAXOELSVPTZZQG-UHFFFAOYSA-N tiglic acid Natural products CC(C)=C(C)C(O)=O UAXOELSVPTZZQG-UHFFFAOYSA-N 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
- XJPBRODHZKDRCB-UHFFFAOYSA-N trans-alpha-ocimene Natural products CC(=C)CCC=C(C)C=C XJPBRODHZKDRCB-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
- 229940070710 valerate Drugs 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-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
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 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
- 229930007850 β-damascenone Natural products 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/005—Compositions containing perfumes; Compositions containing deodorants
-
- 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
- C11B9/0084—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing more than six atoms
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
- D06M13/228—Cyclic esters, e.g. lactones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/10—General cosmetic use
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Textile Engineering (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Dermatology (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
下記一般式(I)で表される化合物を含む組成物であって、前記一般式(I)で表される化合物のE体と前記一般式(I)で表される化合物のZ体の比率がE体/Z体=3/7以上7/3以下である。
以下の実施例及び比較例等において行った測定法の詳細を以下にまとめて示す。
以下の製造例で得られた各化合物は、1H−NMRおよびガスクロマトグラフ質量(GC−MS)分析計(島津製作所社製、型式:GC−2010)のスペクトル分析により得たデータと、公知文献等により開示された化合物データとが合致することにより化合物を同定した。
調香・香料評価業務経験者2名により、におい紙法により香調と強度を判定した。におい紙(幅6mm長さ150mmの香料試験紙)の先端約5mmを、試料に浸漬し、評価した。
E体/Z体の比率が91/9である、オキサシクロヘプタデク―8―エン−2−オン混合物の合成方法
[製造例1]
(a)9−デセニル−7−オクテノアートの製造
フラスコに、9−デセン−1−オール(東京化成工業株式会社製、2.2g、14.0ミリモル)および7−オクテン酸(アルドリッチ社製、2.0g、14.0ミリモル)を仕込み、ジクロロメタン(30mL)に溶解させた。続いて前記フラスコ中に、1−エチル−3(3−ジメチルアミノプロピル)カルボジイミド塩酸塩(3.2g、16.8ミリモル)とN,N'−ジメチルアミノピリジン(171mg、1.4ミリモル)を添加し、窒素気流下、室温で3時間反応させた。反応終了液に塩化アンモニウム水溶液を加えて攪拌後、静置分層して水層を抜き出し、油層を飽和食塩水で洗浄後、硫酸ナトリウムを加えて脱水乾燥した。濾過した後に前記油層からジクロロメタンを留去し、9−デセニル−7−オクテノアート(3.9g、14.0ミリモル)を粗収率100%で得た。
三口フラスコに、前記工程(a)において得られた9−デセニル−7−オクテノアート(3.3g、11.8ミリモル)、ジクロロメタン(3L)、および下記式に示すメタセシス触媒(商品名「Umicore M2」、ユミコアジャパン株式会社製、194mg、0.21ミリモル)を仕込み、窒素気流下24時間加熱還流(50℃)を行った後、下記式に示すメタセシス触媒を130mg(0.14ミリモル)追加添加し、更に5時間撹拌を続けた。反応終了液のガスクロマトグラフィー定量分析を行ったところ、オキサシクロヘプタデク―8―エン−2−オンが2.0g(E/Z=70/30、7.9ミリモル、収率67%)含まれていた。
E体/Z体の比率が2/98であるオキサシクロヘプタデク―8―エン−2−オンの混合物の合成方法
三口フラスコに、製造例1(a)で得られた9−デセニル−7−オクテノアート(0.9g、3.2ミリモル)、ジクロロメタン(1.1L)、および下記式に示すメタセシス触媒(アルドリッチ社製、100mg、0.16ミリモル)を仕込み、窒素気流下24時間加熱還流(50℃)を行った後、下記式に示すメタセシス触媒を100mg(0.16ミリモル)追加添加し、更に24時間撹拌を続けた。反応終了液のガスクロマトグラフィー定量分析を行ったところ、(Z)―オキサシクロヘプタデク―8―エン−2−オンが0.4g(E/Z=2/98、1.6ミリモル、収率49%)含まれていた。
製造例1で得られた化合物(I)の混合物(ただしE体/Z体=91/9)と製造例2で得られた化合物(I)の混合物(ただしE体/Z体=2/98)を用いて、表1に示す組成の組成物を調製し、香気評価を行った。香気評価の結果も表1に示す。
製造例1で得られた化合物(I)の混合物(ただしE体/Z体=91/9)と製造例2で得られた化合物(I)の混合物(ただしE体/Z体=2/98)を用いて、表2に示す組成の香水を調製した。得られた香水の香気評価を行い、その香気評価の結果は表3に示す。
2)D.P.G:ジプロピレングリコール、
3)MDJ(花王株式会社商品名、ジヒドロジャスモン酸メチル、メチル (2−ペンチル−3−オキソシクロペンチル)アセテート)、
4)イソ・イー・スーパー(IFF社商品名、1−(1,2,3,4,5,6,7,8−オクタヒドロ−2,3,8,8−テトラメチル−2−ナフタレニル)−エタン−1−オン)、
5)リファローム(IFF社商品名、cis−3−ヘキセニルメチルカーボネート)、
6)リリアール(Givaudan社商品名、p−tert−ブチル−α−メチルヒドロシンナミックアルデヒド)、
7)ベルートン(フィルメニッヒ社商品名、2,2,5−トリメチル−5−ペンチルシクロペンタノン)、
8)アンバーコア(花王株式会社商品名、1−(2−t−ブチルシクロヘキシルオキシ)−2−ブタノール)、サンダルマイソールコア(花王株式会社商品名、
9)フロローサ(ジボダン社商品名、化学名:4−メチル−2−(2−メチルプロピル)テトラヒドロ−2H−4−ピラノール)。
製造例1で得られた化合物(I)の混合物(ただしE体/Z体=91/9)と製造例2で得られた化合物(I)の混合物(ただしE体/Z体=2/98)を用いて、表4に示す組成の香水を調製した。得られた香水の香気評価を行い、その香気評価の結果は表5に示す。
2)アンブリノール(商品名、1,2,3,4,4a,5,6,7−オクタヒドロ−2,5,5−トリメチル−ナフタレン−2−オール)、
3)アンブリノール20T(高砂香料工業株式会社商品名、1,2,3,4,4a,5,6,7−オクタヒドロ−2,5,5−トリメチル−ナフタレン−2−オール)、
4)アンブロテック(花王株式会社商品名、ドデカヒドロ−3a,6,6,9a−テトラメチルナフト[2,1−b]フラン)、
5)アンブロキサン(花王株式会社商品名、[3aR−(3aα,5aβ,9aα,9bβ)]ドデカヒドロ−3a,6,6,9a−テトラメチルナフト[2,1−b]フラン)、
6)ボアザンブレンフォルテ(花王株式会社商品名、エトキシメチルシクロドデシルエーテル)、
7)D.P.G:ジプロピレングリコール、
8)フロラントンT(高砂香料工業株式会社商品名、1−(5,6,7,8−テトラヒドロ−2−ナフタレニル)エタノン、
9)フロレックス(フィルメニヒ社商品名、6−エチリデンオクタハイドロ−5,8−メタノ−2H−1−ベンゾピラン)、
10)ガラクソリド(IFF社商品名、ヘキサメチルヘキサヒドロシクロペンタベンゾピラン)、
11)グロバノン(シムライズ社商品名、8−シクロヘキサデセノン)、
12)ハバノリド(フィルメニヒ社商品名、シクロペンタデセノリド)、
13)インドレン50BB(IFF社商品名、7,7−ビス(1H−インドール−3−イル)−1,1,5−トリメチル−1−ヘプタノール、
14)l−ムスコン((R)−3−メチルシクロペンタデカノン)、
15)ムスコン(3-メチルシクロペンタデカノン)、
16)ムスクTM−II(曽田香料株式会社商品名、5−シクロヘキサデセン−1−オン)、
17)ムスクZ−4(IFF社商品名、(Z)−4−シクロペンタデセン−1−オン)、
18)ポリメフロール(高砂香料工業株式会社商品名、1−(2−メチル−2−プロペニルオキシ)−2,2,4−トリメチルペンタン−3−オール)
製造例1で得られた化合物(I)の混合物(ただしE体/Z体=91/9)と製造例2で得られた化合物(I)の混合物(ただしE体/Z体=2/98)を用いて、表6に示す組成の香水を調製した。得られた香水の香気評価を行い、その香気評価の結果は表7に示す。
2)I.P.M(ミリスチン酸イソプロピル)、
3)MDJ(花王株式会社商品名、ジヒドロジャスモン酸メチル、メチル (2−ペンチル−3−オキソシクロペンチル)アセテート)、
4)トリプラール(IFF商品名、2,4−ジメチル−3−シクロヘキセン−1−カルボキシアルデヒド)
5)べルートン(フィルメニヒ社商品名、2,5,5−トリメチル−2−ペンチルシクロペンタノン)
Claims (10)
- 前記一般式(I)で表される化合物のE体と前記一般式(I)で表される化合物のZ体の比率が、E体/Z体=5/5以上7/3以下である請求項1に記載の組成物。
- 一般式(I)で表される化合物以外の香料を含有し、前記一般式(I)で表される化合物の含有量が、0.01質量%以上25質量%以下である請求項1又は2に記載の組成物。
- 前記一般式(I)で表される化合物以外の香料が、炭化水素類、アルコール類、フェノール類、アルデヒド類、ケトン類、アセタール類、エーテル類、エステル類、カーボネート類、化合物(I)を除くラクトン類、カルボン酸類、ニトリル類、シッフ塩基類、天然精油および天然抽出物のうち1種以上である、請求項3に記載の組成物。
- 請求項1〜4いずれか一項記載の組成物を含有する洗浄剤。
- 請求項1〜4いずれか一項記載の組成物を含有する化粧料。
- 請求項1〜4いずれか一項記載の組成物を含有する繊維処理剤。
- 請求項1〜4いずれか一項記載の組成物を賦香成分として使用する方法。
- 請求項1〜4いずれか一項記載の組成物を賦香成分として香り全体を強める方法。
- 請求項1〜4いずれか一項記載の組成物を賦香成分としてムスクの柔らかさを足す方法。
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EP0908455B1 (de) * | 1997-10-09 | 2002-07-10 | Givaudan SA | Macrocyclen |
FR2775285B1 (fr) | 1998-02-20 | 2000-04-14 | Synarome H Fraysse Et Cie | Procede de fabrication de la cis-isoambrettolide et son application |
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CN111936608A (zh) | 2020-11-13 |
EP3778843A1 (en) | 2021-02-17 |
CN111936608B (zh) | 2024-01-09 |
US20210163845A1 (en) | 2021-06-03 |
EP3778843A4 (en) | 2021-12-22 |
JP7319967B2 (ja) | 2023-08-02 |
US11352588B2 (en) | 2022-06-07 |
WO2019194186A1 (ja) | 2019-10-10 |
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