JP2010104765A - 芳香性組成物 - Google Patents
芳香性組成物 Download PDFInfo
- Publication number
- JP2010104765A JP2010104765A JP2009087340A JP2009087340A JP2010104765A JP 2010104765 A JP2010104765 A JP 2010104765A JP 2009087340 A JP2009087340 A JP 2009087340A JP 2009087340 A JP2009087340 A JP 2009087340A JP 2010104765 A JP2010104765 A JP 2010104765A
- Authority
- JP
- Japan
- Prior art keywords
- lactone
- fragrance
- ketone
- methyl
- fragrances
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 83
- 125000003118 aryl group Chemical group 0.000 title abstract description 16
- 239000003205 fragrance Substances 0.000 claims abstract description 203
- 150000002596 lactones Chemical class 0.000 claims abstract description 109
- 150000002576 ketones Chemical class 0.000 claims abstract description 63
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 50
- 239000011630 iodine Substances 0.000 claims abstract description 50
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 50
- -1 aliphatic ketones Chemical class 0.000 claims description 103
- 239000003755 preservative agent Substances 0.000 claims description 52
- 230000002335 preservative effect Effects 0.000 claims description 43
- 125000000217 alkyl group Chemical group 0.000 claims description 34
- 125000004432 carbon atom Chemical group C* 0.000 claims description 26
- PHXATPHONSXBIL-UHFFFAOYSA-N xi-gamma-Undecalactone Chemical compound CCCCCCCC1CCC(=O)O1 PHXATPHONSXBIL-UHFFFAOYSA-N 0.000 claims description 16
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 claims description 15
- VMUXSMXIQBNMGZ-UHFFFAOYSA-N 3,4-dihydrocoumarin Chemical class C1=CC=C2OC(=O)CCC2=C1 VMUXSMXIQBNMGZ-UHFFFAOYSA-N 0.000 claims description 13
- DMSHWWDRAYHEBS-UHFFFAOYSA-N dihydrocoumarin Chemical class C1CC(=O)OC2=C1C=C(OC)C(OC)=C2 DMSHWWDRAYHEBS-UHFFFAOYSA-N 0.000 claims description 13
- LOKPJYNMYCVCRM-UHFFFAOYSA-N 16-Hexadecanolide Chemical compound O=C1CCCCCCCCCCCCCCCO1 LOKPJYNMYCVCRM-UHFFFAOYSA-N 0.000 claims description 12
- XPCTZQVDEJYUGT-UHFFFAOYSA-N 3-hydroxy-2-methyl-4-pyrone Chemical compound CC=1OC=CC(=O)C=1O XPCTZQVDEJYUGT-UHFFFAOYSA-N 0.000 claims description 12
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 claims description 12
- QRPLZGZHJABGRS-UHFFFAOYSA-N xi-5-Dodecanolide Chemical compound CCCCCCCC1CCCC(=O)O1 QRPLZGZHJABGRS-UHFFFAOYSA-N 0.000 claims description 12
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims description 10
- 235000001671 coumarin Nutrition 0.000 claims description 10
- 229960000956 coumarin Drugs 0.000 claims description 10
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 claims description 9
- 239000002304 perfume Substances 0.000 claims description 9
- 229940099451 3-iodo-2-propynylbutylcarbamate Drugs 0.000 claims description 8
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 claims description 8
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 8
- PHXATPHONSXBIL-JTQLQIEISA-N gamma-Undecalactone Natural products CCCCCCC[C@H]1CCC(=O)O1 PHXATPHONSXBIL-JTQLQIEISA-N 0.000 claims description 8
- 229940020436 gamma-undecalactone Drugs 0.000 claims description 8
- 235000007586 terpenes Nutrition 0.000 claims description 8
- HFOCAQPWSXBFFN-UHFFFAOYSA-N 2-methylsulfonylbenzaldehyde Chemical compound CS(=O)(=O)C1=CC=CC=C1C=O HFOCAQPWSXBFFN-UHFFFAOYSA-N 0.000 claims description 7
- PFDVPCSDZXZDMF-UHFFFAOYSA-N 4-methyl-4-phenylpentan-2-one Chemical compound CC(=O)CC(C)(C)C1=CC=CC=C1 PFDVPCSDZXZDMF-UHFFFAOYSA-N 0.000 claims description 7
- GJJSUPSPZIZYPM-UHFFFAOYSA-N 1,4-dioxacyclohexadecane-5,16-dione Chemical compound O=C1CCCCCCCCCCC(=O)OCCO1 GJJSUPSPZIZYPM-UHFFFAOYSA-N 0.000 claims description 6
- MZLRFHKWWCSGHB-UHFFFAOYSA-N 1,8-dioxacycloheptadecan-9-one Chemical compound O=C1CCCCCCCCOCCCCCCO1 MZLRFHKWWCSGHB-UHFFFAOYSA-N 0.000 claims description 6
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 claims description 6
- ZFKUTGNRVJOCIO-UHFFFAOYSA-N 3-Heptyldihydro-5-methyl-2(3H)-furanone Chemical compound CCCCCCCC1CC(C)OC1=O ZFKUTGNRVJOCIO-UHFFFAOYSA-N 0.000 claims description 6
- WGPCZPLRVAWXPW-NSHDSACASA-N 5-octyloxolan-2-one Chemical compound CCCCCCCC[C@H]1CCC(=O)O1 WGPCZPLRVAWXPW-NSHDSACASA-N 0.000 claims description 6
- YZRXRLLRSPQHDK-UHFFFAOYSA-N 6-Hexyltetrahydro-2H-pyran-2-one Chemical compound CCCCCCC1CCCC(=O)O1 YZRXRLLRSPQHDK-UHFFFAOYSA-N 0.000 claims description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005977 Ethylene Substances 0.000 claims description 6
- HYMLWHLQFGRFIY-UHFFFAOYSA-N Maltol Natural products CC1OC=CC(=O)C1=O HYMLWHLQFGRFIY-UHFFFAOYSA-N 0.000 claims description 6
- 230000002421 anti-septic effect Effects 0.000 claims description 6
- 150000003997 cyclic ketones Chemical class 0.000 claims description 6
- SKQYTJLYRIFFCO-UHFFFAOYSA-N delta-Tetradecalactone Chemical compound CCCCCCCCCC1CCCC(=O)O1 SKQYTJLYRIFFCO-UHFFFAOYSA-N 0.000 claims description 6
- WGPCZPLRVAWXPW-LLVKDONJSA-N gamma-Dodecalactone Natural products CCCCCCCC[C@@H]1CCC(=O)O1 WGPCZPLRVAWXPW-LLVKDONJSA-N 0.000 claims description 6
- SRIFJCOBFTWCTM-UHFFFAOYSA-N gamma-hexadecanolactone Natural products CCCCCCCCCCCCC1CCC(=O)O1 SRIFJCOBFTWCTM-UHFFFAOYSA-N 0.000 claims description 6
- 229940043353 maltol Drugs 0.000 claims description 6
- 229930004725 sesquiterpene Natural products 0.000 claims description 6
- PSQYTAPXSHCGMF-BQYQJAHWSA-N β-ionone Chemical compound CC(=O)\C=C\C1=C(C)CCCC1(C)C PSQYTAPXSHCGMF-BQYQJAHWSA-N 0.000 claims description 6
- NFLGAXVYCFJBMK-RKDXNWHRSA-N (+)-isomenthone Natural products CC(C)[C@H]1CC[C@@H](C)CC1=O NFLGAXVYCFJBMK-RKDXNWHRSA-N 0.000 claims description 5
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims description 5
- QQLIGMASAVJVON-UHFFFAOYSA-N 1-naphthalen-1-ylethanone Chemical compound C1=CC=C2C(C(=O)C)=CC=CC2=C1 QQLIGMASAVJVON-UHFFFAOYSA-N 0.000 claims description 5
- PJXHBTZLHITWFX-UHFFFAOYSA-N 2-heptylcyclopentan-1-one Chemical compound CCCCCCCC1CCCC1=O PJXHBTZLHITWFX-UHFFFAOYSA-N 0.000 claims description 5
- VNWOJVJCRAHBJJ-UHFFFAOYSA-N 2-pentylcyclopentan-1-one Chemical compound CCCCCC1CCCC1=O VNWOJVJCRAHBJJ-UHFFFAOYSA-N 0.000 claims description 5
- OAFJAALOFJVHMK-UHFFFAOYSA-N 4-cyclohexyl-4-methylpentan-2-one Chemical compound CC(=O)CC(C)(C)C1CCCCC1 OAFJAALOFJVHMK-UHFFFAOYSA-N 0.000 claims description 5
- 241000723346 Cinnamomum camphora Species 0.000 claims description 5
- NFLGAXVYCFJBMK-UHFFFAOYSA-N Menthone Chemical compound CC(C)C1CCC(C)CC1=O NFLGAXVYCFJBMK-UHFFFAOYSA-N 0.000 claims description 5
- 150000008365 aromatic ketones Chemical class 0.000 claims description 5
- 229960000846 camphor Drugs 0.000 claims description 5
- 229930008380 camphor Natural products 0.000 claims description 5
- 229930007503 menthone Natural products 0.000 claims description 5
- CEPZWWNWJNBTIM-UHFFFAOYSA-N (3-bromo-2,3-diiodoprop-2-enyl) ethyl carbonate Chemical compound CCOC(=O)OCC(I)=C(Br)I CEPZWWNWJNBTIM-UHFFFAOYSA-N 0.000 claims description 4
- XOILGBPDXMVFIP-UHFFFAOYSA-N 1-(diiodomethylsulfonyl)-4-methylbenzene Chemical compound CC1=CC=C(S(=O)(=O)C(I)I)C=C1 XOILGBPDXMVFIP-UHFFFAOYSA-N 0.000 claims description 4
- SQRDRPSVGROPHX-UHFFFAOYSA-N 2,3,3-triiodoprop-2-en-1-ol Chemical compound OCC(I)=C(I)I SQRDRPSVGROPHX-UHFFFAOYSA-N 0.000 claims description 4
- RZZLMGATMUAJPX-UHFFFAOYSA-N Delta-Tridecalactone Chemical compound CCCCCCCCC1CCCC(=O)O1 RZZLMGATMUAJPX-UHFFFAOYSA-N 0.000 claims description 4
- BBXKBKXJLXJZIQ-UHFFFAOYSA-N phenyl 11-iodoundec-10-enoate Chemical compound C1(=CC=CC=C1)OC(CCCCCCCCC=CI)=O BBXKBKXJLXJZIQ-UHFFFAOYSA-N 0.000 claims description 4
- SFEOKXHPFMOVRM-UHFFFAOYSA-N (+)-(S)-gamma-ionone Natural products CC(=O)C=CC1C(=C)CCCC1(C)C SFEOKXHPFMOVRM-UHFFFAOYSA-N 0.000 claims description 3
- MKEIDVFLAWJKMY-UHFFFAOYSA-N 1,7-dioxacycloheptadecan-8-one Chemical compound O=C1CCCCCCCCCOCCCCCO1 MKEIDVFLAWJKMY-UHFFFAOYSA-N 0.000 claims description 3
- ZCPRKFXONQQHRM-UHFFFAOYSA-N C(C(C#CC(Br)I)I)NC(=O)O Chemical compound C(C(C#CC(Br)I)I)NC(=O)O ZCPRKFXONQQHRM-UHFFFAOYSA-N 0.000 claims description 3
- CTETYYAZBPJBHE-UHFFFAOYSA-N Haloprogin Chemical compound ClC1=CC(Cl)=C(OCC#CI)C=C1Cl CTETYYAZBPJBHE-UHFFFAOYSA-N 0.000 claims description 3
- 125000002950 monocyclic group Chemical group 0.000 claims description 3
- 229930186686 Jasmolactone Natural products 0.000 claims description 2
- 150000004775 coumarins Chemical class 0.000 claims description 2
- 125000000332 coumarinyl group Chemical group O1C(=O)C(=CC2=CC=CC=C12)* 0.000 claims description 2
- NBCMACYORPIYNY-UHFFFAOYSA-N jasmolactone Chemical compound CC=CCCC1CCCC(=O)O1 NBCMACYORPIYNY-UHFFFAOYSA-N 0.000 claims description 2
- BEKNOGMQVKBMQN-UHFFFAOYSA-N 2-methyl-2,3-dihydroinden-1-one Chemical compound C1=CC=C2C(=O)C(C)CC2=C1 BEKNOGMQVKBMQN-UHFFFAOYSA-N 0.000 claims 1
- 241000233866 Fungi Species 0.000 abstract description 17
- 239000004599 antimicrobial Substances 0.000 abstract description 4
- 230000035755 proliferation Effects 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 12
- 239000000796 flavoring agent Substances 0.000 description 12
- 235000019634 flavors Nutrition 0.000 description 12
- 239000003921 oil Substances 0.000 description 11
- 235000019198 oils Nutrition 0.000 description 11
- 241000894006 Bacteria Species 0.000 description 10
- 229940022663 acetate Drugs 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 7
- 230000000843 anti-fungal effect Effects 0.000 description 7
- 239000002781 deodorant agent Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 6
- RHLVCLIPMVJYKS-UHFFFAOYSA-N 3-octanone Chemical compound CCCCCC(=O)CC RHLVCLIPMVJYKS-UHFFFAOYSA-N 0.000 description 6
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 description 6
- NTPLXRHDUXRPNE-UHFFFAOYSA-N 4-methoxyacetophenone Chemical compound COC1=CC=C(C(C)=O)C=C1 NTPLXRHDUXRPNE-UHFFFAOYSA-N 0.000 description 5
- 230000000844 anti-bacterial effect Effects 0.000 description 5
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 description 5
- 239000000077 insect repellent Substances 0.000 description 5
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
- 229940098465 tincture Drugs 0.000 description 5
- MRMOPGVGWFNHIN-UHFFFAOYSA-N 1,6-dioxacycloheptadecan-7-one Chemical compound O=C1CCCCCCCCCCOCCCCO1 MRMOPGVGWFNHIN-UHFFFAOYSA-N 0.000 description 4
- WFWKNGZODAOLEO-UHFFFAOYSA-N 1-(4-Methoxyphenyl)-2-propanone Chemical compound COC1=CC=C(CC(C)=O)C=C1 WFWKNGZODAOLEO-UHFFFAOYSA-N 0.000 description 4
- KEFJLCGVTHRGAH-UHFFFAOYSA-N 2-acetyl-5-methylfuran Chemical compound CC(=O)C1=CC=C(C)O1 KEFJLCGVTHRGAH-UHFFFAOYSA-N 0.000 description 4
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 4
- WGAVDEVFJDQIMZ-UHFFFAOYSA-N 3,4-dimethyl-1,2-cyclopentanedione Chemical compound CC1CC(=O)C(=O)C1C WGAVDEVFJDQIMZ-UHFFFAOYSA-N 0.000 description 4
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- 241000402754 Erythranthe moschata Species 0.000 description 4
- CRZQGDNQQAALAY-UHFFFAOYSA-N Methyl benzeneacetate Chemical compound COC(=O)CC1=CC=CC=C1 CRZQGDNQQAALAY-UHFFFAOYSA-N 0.000 description 4
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- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
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- 239000000194 fatty acid Substances 0.000 description 4
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- 239000007788 liquid Substances 0.000 description 3
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- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
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- NZGWDASTMWDZIW-MRVPVSSYSA-N (+)-pulegone Chemical compound C[C@@H]1CCC(=C(C)C)C(=O)C1 NZGWDASTMWDZIW-MRVPVSSYSA-N 0.000 description 2
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 description 2
- XHXUANMFYXWVNG-ADEWGFFLSA-N (-)-Menthyl acetate Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(C)=O XHXUANMFYXWVNG-ADEWGFFLSA-N 0.000 description 2
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- JDQVBGQWADMTAM-UHFFFAOYSA-N phenethyl isobutyrate Chemical compound CC(C)C(=O)OCCC1=CC=CC=C1 JDQVBGQWADMTAM-UHFFFAOYSA-N 0.000 description 1
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- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
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- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
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- 229920001296 polysiloxane Polymers 0.000 description 1
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- 238000002360 preparation method Methods 0.000 description 1
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- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
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- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 235000019721 spearmint oil Nutrition 0.000 description 1
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- 239000007921 spray Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010676 star anise oil Substances 0.000 description 1
- 239000008227 sterile water for injection Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- PINIEAOMWQJGBW-FYZOBXCZSA-N tenofovir hydrate Chemical compound O.N1=CN=C2N(C[C@@H](C)OCP(O)(O)=O)C=NC2=C1N PINIEAOMWQJGBW-FYZOBXCZSA-N 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- UPRLOYNUXQZAPJ-LURJTMIESA-N tert-butyl (2s)-2-hydroxybutanoate Chemical compound CC[C@H](O)C(=O)OC(C)(C)C UPRLOYNUXQZAPJ-LURJTMIESA-N 0.000 description 1
- 239000010678 thyme oil Substances 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229960000984 tocofersolan Drugs 0.000 description 1
- MBDOYVRWFFCFHM-UHFFFAOYSA-N trans-2-hexenal Natural products CCCC=CC=O MBDOYVRWFFCFHM-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
- IUSBVFZKQJGVEP-UHFFFAOYSA-N trans-isoeugenol acetate Natural products COC1=CC(C=CC)=CC=C1OC(C)=O IUSBVFZKQJGVEP-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
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
- A23F3/00—Tea; Tea substitutes; Preparations thereof
- A23F3/06—Treating tea before extraction; Preparations produced thereby
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
- A23F3/00—Tea; Tea substitutes; Preparations thereof
- A23F3/06—Treating tea before extraction; Preparations produced thereby
- A23F3/08—Oxidation; Fermentation
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Biotechnology (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Fats And Perfumes (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Seasonings (AREA)
- Cosmetics (AREA)
Abstract
【解決手段】本発明により、ラクトン系香料および/またはケトン系香料、ならびに有機ヨード系防腐剤を含む水性芳香性組成物であって、香料に含まれるラクトン系香料の重量の1/500およびケトン系香料の重量の1/50の合計の重量以上の有機ヨード系防腐剤を含む、前記組成物が提供される。さらに、本発明により、ラクトン系香料および/またはケトン系香料を含む水性芳香性組成物における菌類および/または真菌類の繁殖防止のために使用する、有機ヨード系防腐剤が提供される。
【選択図】なし
Description
A4)C1−10アルキルで置換されていてもよく、ラクトンを形成する環炭素原子数が3〜16である単環式または多環式ラクトンであるラクトン系香料;および脂肪族ケトン、テルペン系ケトン、セスキテルペン系ケトン、環状ケトン、または芳香族ケトンであるケトン系香料から選択される少なくとも一種の香料を含む、上記A1)〜A3)のいずれかに記載の組成物。
A11)マルトール、メチルアミルケトン、コアボン、カンファー、メントン、β−イオノン、セドリルメチルケトン、アミルシクロペンタノン、ヘプチルシクロペンタノン、4−シクロヘキシル−4−メチル−2−ペンタノン、ジヒドロペンタメチルインダノン、トリモフィクス、アセトフェノン、4−フェニル−4−メチル−2−ペンタノン、およびメチルナフチルケトンから選択される少なくとも一種のケトン系香料を含む、上記A1)〜A9)のいずれかに記載の組成物。
本発明の別の側面によれば、以下のB1)〜B13)に記載される有機ヨード系防腐剤が提供される。
B12)水性芳香性組成物全体に対して0.001〜8重量%の量で使用される、上記B1)〜B11)のいずれかに記載の有機ヨード系防腐剤。
例えば、カルボニル基を1つ含む脂肪族ケトンとして、アセトイン、メチルアミルケトン、エチルアミルケトン、メチルヘキシルケトン、メチルノニルケトン、メチルヘプテノン、コアボン、2−ペンタノン、3−ヘキサノン、2−ヘプタノン、3−ヘプタノン、4−ヘプタノン、2−オクタノン、3−オクタノン、2−ノナノン、3−ノナノン、2−ウンデカノン、メチルイソプロピルケトン、エチルイソアミルケトン、2−トリデカノン、メシチルオキサイド、ブチリデンアセトン、メチルヘプタジエノン、ジメチルオクテノン、5−ヒドロキシ−4−オクタノン(ブチロイン)、および3−ヒドロキシメチル−2−ノナノンが挙げられる。
炭化水素系香料:d−リモネン、カリオフィレン、α−ピネン、β−ピネン、ミルセン、ターピノレン、オシメン、γ−ターピネン、α−フェランドレン、p−サイメン、β−カリオフィレン、β−ファルネセン、1,3,5−ウンデカトリエン、ジフェニルメタンなど。
ムスク系香料:ムスクキシロール、ムスクアンブレット、ムスクチベテン、ムスクモスケン、6−アセチルヘキサメチルインダン、4−アセチルジメチル−t−ブチルインダン、5−アセチルテトラメチルイソプロプルインダン、6−アセチルヘキサテトラリン、ヘキサメチルヘキサヒドロシクロペンタンベンゾピランなど。
界面活性剤の例としては、非イオン性界面活性剤(例えば、ポリオキシアルキレンデシルエーテル、ポリオキシアルキレン硬化ヒマシ油エーテル、ポリオキシアルキレンラウリルエーテル、ポリオキシエチレントリデシルエーテル、ポリオキシアルキレントリデシルエーテル、ポリオキシアルキレンアルキルエーテル、ポリオキシエチレンラウリルエーテル、ポリオキシエチレンスチレン化フェニルエーテル、ポリオキシエチレンイソデシルエーテル、ポリオキシエチレンアルキルエーテル、ポリオキシエチレンオレイルセチルエーテル、ポリオキシエチレンポリオキシプロピレンブロックポリマー、ソルビタン脂肪酸エステル、ポリオキシエチレンソルビタン脂肪酸エステル、ポリオキシエチレンオレイン酸エステル、ポリオキシエチレンジステアリン酸エステル、ポリオキシエチレンヒマシ油、ポリオキシエチレン硬化ヒマシ油、ポリオキシエチレンラノリンアルコールエーテル、ポリオキシエチレンラノリン脂肪酸エステル、ポリオキシエチレンアルキルアミンエーテル、ヤシ油脂肪酸ジエタノールアミド;および陰イオン性界面活性剤(例えば、ジ(2−エチルヘキシル)スルホコハク酸ナトリウム、ジオクチルスルホサクシネートナトリウム、ラウリル硫酸ナトリウム、アルキル硫酸トリエタノールアミン、ポリオキシエチレンラウリルエーテル硫酸ナトリウム、ポリオキシエチレンアルキルエーテル硫酸ナトリウム、ポリオキシエチレントリデシルエーテル硫酸ナトリウム、スルホコハク酸ラウリル2ナトリウム、ポリオキシエチレンスルホコハク酸ラウリル2ナトリウム、N−ラウロイルサルコシンナトリウム、ポリオキシエチレンラウリルエーテル酢酸ナトリウム、カリウムせっけん用素地、ドデシルベンゼンスルホン酸ナトリウム、アルファオレフィンスルホン酸ナトリウム、ポリオキシエチレンラウリルエーテルリン酸、ポリオキシエチレンアルキルエーテルリン酸が挙げられる。
Claims (12)
- ラクトン系香料およびケトン系香料から選択される1以上の香料、ならびに有機ヨード系防腐剤を含む水性芳香性組成物であって、香料に含まれるラクトン系香料の重量の1/500およびケトン系香料の重量の1/50の合計の重量以上の有機ヨード系防腐剤を含む、前記組成物。
- 有機ヨード系防腐剤が、4−クロルフェニル−3−ヨードプロパルギルホルマール、1−[(ジヨードメチル)スルホニル〕−4−メチルベンゼン、2,4,5−トリクロロフェニルヨードプロパルギルエーテル、2,3,3−トリヨードアリルアルコール、1−ブロム−3−エトキシカルボニルオキシ−1,2−ジヨード−1−プロペン、3−ヨード−2−プロピニルブチルカーバメート、フェニル−11−ヨード−10−ウンデセノエート、ジヨードメチル p−トリルスルホン、および3−ブロモ−2,3−ジヨード−2−プロピニルエチルカーバメートから選択される、請求項1に記載の組成物。
- 有機ヨード系防腐剤を0.001〜8重量%の含有量で含む、請求項1または2に記載の組成物。
- C1−10アルキルで置換されていてもよく、ラクトンを形成する環炭素原子数が3〜16である単環式または多環式ラクトンであるラクトン系香料;および脂肪族ケトン、テルペン系ケトン、セスキテルペン系ケトン、環状ケトン、または芳香族ケトンであるケトン系香料から選択される少なくとも一種の香料を含む、請求項1〜3のいずれか1項に記載の組成物。
- ラクトン系香料として、C1−10アルキルで置換されていてもよいクマリンおよびジヒドロクマリン;C1−10アルキルで置換されていてもよく、ラクトンを形成する環炭素原子数が3〜5である分子量が180以上のラクトン;およびC1−10アルキルで置換されていてもよく、ラクトンを形成する環炭素原子数が14〜16の大員環構造のラクトンからなる群より選択される少なくとも一種を含有する、請求項1〜4のいずれか1項に記載の組成物。
- ラクトン系香料が、C1−10アルキルで置換されていてもよいクマリンおよびジヒドロクマリンである、請求項1〜5のいずれか1項に記載の組成物。
- ラクトン系香料が、C1−10アルキルで置換されていてもよく、ラクトンを形成する環炭素原子数が3〜5である分子量が180以上のラクトンである、請求項1〜5のいずれか1項に記載の組成物。
- ラクトン系香料が、C1−10アルキルで置換されていてもよく、ラクトンを形成する環炭素原子数が14〜16の大員環構造のラクトンである、請求項1〜5のいずれか1項に記載の組成物。
- ラクトン系香料として、クマリン、ジヒドロクマリン、γ−ウンデカラクトン、γ−ドデカラクトン、シスジャスモラクトン、メチル−γ−デカラクトン、δ−ウンデカラクトン、δ−ドデカラクトン、δ−トリデカラクトン、δ−テトラデカラクトン、α−ヘプチル−γ−バレロラクトン、γ−ヘキサデカラクトン、シクロペンタデカノリド、12−ケトシクロペンタデカノリド、シクロヘキサデカノリド、シクロヘキサデセノリド、12−オキサ−16−ヘキサデカノリド、11−オキサ−16−ヘキサデカノリド、10−オキサ−16−ヘキサデカノリド、エチレンブラシレート、エチレンドデカンジオエートからなる群より選択される少なくとも一種を含有する、請求項1〜5のいずれか1項に記載の組成物。
- 分子内にカルボニル基を1つ有するケトンから選択される少なくとも一種のケトン系香料を含む、請求項1〜9のいずれか1項に記載の組成物。
- ケトン系香料として、マルトール、メチルアミルケトン、コアボン、カンファー、メントン、β−イオノン、セドリルメチルケトン、アミルシクロペンタノン、ヘプチルシクロペンタノン、4−シクロヘキシル−4−メチル−2−ペンタノン、ジヒドロペンタメチルインダノン、トリモフィクス、アセトフェノン、4−フェニル−4−メチル−2−ペンタノン、およびメチルナフチルケトンからなる群より選択される少なくとも一種を含有する、請求項1〜9のいずれか1項に記載の組成物。
- 香料がラクトン系香料またはケトン系香料のいずれかを含まない、請求項1〜11のいずれか1項に記載の組成物。
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JP2020196683A (ja) * | 2019-06-03 | 2020-12-10 | 三井化学株式会社 | 水溶液及び抗菌剤 |
JP2020196684A (ja) * | 2019-06-03 | 2020-12-10 | 三井化学株式会社 | ジヨードメタン化合物の水溶液の製造方法 |
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