JP2004513153A5 - - Google Patents
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- JP2004513153A5 JP2004513153A5 JP2002540763A JP2002540763A JP2004513153A5 JP 2004513153 A5 JP2004513153 A5 JP 2004513153A5 JP 2002540763 A JP2002540763 A JP 2002540763A JP 2002540763 A JP2002540763 A JP 2002540763A JP 2004513153 A5 JP2004513153 A5 JP 2004513153A5
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- Prior art keywords
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- weight
- alcohol
- acid
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- Prior art date
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- 239000000203 mixture Substances 0.000 claims 43
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims 42
- 239000003814 drug Substances 0.000 claims 41
- 229940079593 drug Drugs 0.000 claims 40
- 230000000844 anti-bacterial effect Effects 0.000 claims 35
- 239000000796 flavoring agent Substances 0.000 claims 34
- 235000019634 flavors Nutrition 0.000 claims 34
- -1 β-γ-hexanol Chemical compound 0.000 claims 26
- 235000019441 ethanol Nutrition 0.000 claims 25
- 239000003205 fragrance Substances 0.000 claims 22
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 21
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 16
- 235000013824 polyphenols Nutrition 0.000 claims 15
- 239000002253 acid Substances 0.000 claims 14
- 235000019445 benzyl alcohol Nutrition 0.000 claims 14
- 239000000341 volatile oil Substances 0.000 claims 12
- 239000000284 extract Substances 0.000 claims 11
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 10
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 claims 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 9
- 150000001298 alcohols Chemical class 0.000 claims 9
- 230000001476 alcoholic effect Effects 0.000 claims 8
- 150000001299 aldehydes Chemical class 0.000 claims 8
- 150000002148 esters Chemical class 0.000 claims 8
- 229960003742 phenol Drugs 0.000 claims 8
- 239000003795 chemical substances by application Substances 0.000 claims 7
- 239000003921 oil Substances 0.000 claims 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 6
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 6
- 241001465754 Metazoa Species 0.000 claims 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 6
- 150000001241 acetals Chemical class 0.000 claims 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims 6
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 claims 6
- 239000002304 perfume Substances 0.000 claims 6
- 150000003505 terpenes Chemical class 0.000 claims 6
- 235000007586 terpenes Nutrition 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 5
- 238000004519 manufacturing process Methods 0.000 claims 5
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 claims 5
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 claims 4
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 claims 4
- OIGWAXDAPKFNCQ-UHFFFAOYSA-N 4-isopropylbenzyl alcohol Chemical compound CC(C)C1=CC=C(CO)C=C1 OIGWAXDAPKFNCQ-UHFFFAOYSA-N 0.000 claims 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 4
- ROWKJAVDOGWPAT-UHFFFAOYSA-N Acetoin Chemical compound CC(O)C(C)=O ROWKJAVDOGWPAT-UHFFFAOYSA-N 0.000 claims 4
- SCCDQYPEOIRVGX-UHFFFAOYSA-N Acetyleugenol Chemical compound COC1=CC(CC=C)=CC=C1OC(C)=O SCCDQYPEOIRVGX-UHFFFAOYSA-N 0.000 claims 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 claims 4
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 claims 4
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 claims 4
- REFJWTPEDVJJIY-UHFFFAOYSA-N Quercetin Chemical compound C=1C(O)=CC(O)=C(C(C=2O)=O)C=1OC=2C1=CC=C(O)C(O)=C1 REFJWTPEDVJJIY-UHFFFAOYSA-N 0.000 claims 4
- 229940022663 acetate Drugs 0.000 claims 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 claims 4
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 claims 4
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims 4
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 claims 4
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims 4
- 229960004592 isopropanol Drugs 0.000 claims 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims 4
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 claims 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims 4
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 claims 4
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 claims 4
- LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical compound OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 claims 4
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 claims 4
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 claims 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 4
- 229920001864 tannin Polymers 0.000 claims 4
- 235000018553 tannin Nutrition 0.000 claims 4
- 239000001648 tannin Substances 0.000 claims 4
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 claims 4
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims 4
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 claims 3
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 claims 3
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims 3
- MSHFRERJPWKJFX-UHFFFAOYSA-N 4-Methoxybenzyl alcohol Chemical compound COC1=CC=C(CO)C=C1 MSHFRERJPWKJFX-UHFFFAOYSA-N 0.000 claims 3
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 claims 3
- 244000223760 Cinnamomum zeylanicum Species 0.000 claims 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 3
- IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 claims 3
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims 3
- 150000007513 acids Chemical class 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 claims 3
- 229930016911 cinnamic acid Natural products 0.000 claims 3
- 235000013985 cinnamic acid Nutrition 0.000 claims 3
- 235000017803 cinnamon Nutrition 0.000 claims 3
- 235000000484 citronellol Nutrition 0.000 claims 3
- 201000010099 disease Diseases 0.000 claims 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 3
- 239000001530 fumaric acid Substances 0.000 claims 3
- 229960002598 fumaric acid Drugs 0.000 claims 3
- 235000011087 fumaric acid Nutrition 0.000 claims 3
- 230000000855 fungicidal effect Effects 0.000 claims 3
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims 3
- XJNUECKWDBNFJV-UHFFFAOYSA-N hexadecyl 2-ethylhexanoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C(CC)CCCC XJNUECKWDBNFJV-UHFFFAOYSA-N 0.000 claims 3
- 229960002510 mandelic acid Drugs 0.000 claims 3
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims 3
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 claims 3
- 235000013772 propylene glycol Nutrition 0.000 claims 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 3
- FQTLCLSUCSAZDY-UHFFFAOYSA-N (+) E(S) nerolidol Natural products CC(C)=CCCC(C)=CCCC(C)(O)C=C FQTLCLSUCSAZDY-UHFFFAOYSA-N 0.000 claims 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 claims 2
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 claims 2
- RGZSQWQPBWRIAQ-CABCVRRESA-N (-)-alpha-Bisabolol Chemical compound CC(C)=CCC[C@](C)(O)[C@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-CABCVRRESA-N 0.000 claims 2
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 claims 2
- 239000001500 (2R)-6-methyl-2-[(1R)-4-methyl-1-cyclohex-3-enyl]hept-5-en-2-ol Substances 0.000 claims 2
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 claims 2
- 239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 claims 2
- 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 2
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 claims 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims 2
- SWTCCCJQNPGXLQ-UHFFFAOYSA-N 1-(1-butoxyethoxy)butane Chemical compound CCCCOC(C)OCCCC SWTCCCJQNPGXLQ-UHFFFAOYSA-N 0.000 claims 2
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 claims 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims 2
- WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 claims 2
- GIEMHYCMBGELGY-UHFFFAOYSA-N 10-undecen-1-ol Chemical compound OCCCCCCCCCC=C GIEMHYCMBGELGY-UHFFFAOYSA-N 0.000 claims 2
- XYHKNCXZYYTLRG-UHFFFAOYSA-N 1h-imidazole-2-carbaldehyde Chemical compound O=CC1=NC=CN1 XYHKNCXZYYTLRG-UHFFFAOYSA-N 0.000 claims 2
- MBDOYVRWFFCFHM-UHFFFAOYSA-N 2-hexenal Chemical compound CCCC=CC=O MBDOYVRWFFCFHM-UHFFFAOYSA-N 0.000 claims 2
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 claims 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 claims 2
- GWYFCOCPABKNJV-UHFFFAOYSA-M 3-Methylbutanoic acid Natural products CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 claims 2
- VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-Phenyl-1-propanol Chemical compound OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 claims 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims 2
- 241000723346 Cinnamomum camphora Species 0.000 claims 2
- 235000005979 Citrus limon Nutrition 0.000 claims 2
- 244000131522 Citrus pyriformis Species 0.000 claims 2
- 208000035473 Communicable disease Diseases 0.000 claims 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 2
- 239000001263 FEMA 3042 Substances 0.000 claims 2
- 239000005792 Geraniol Substances 0.000 claims 2
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 claims 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims 2
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 claims 2
- 244000062730 Melissa officinalis Species 0.000 claims 2
- FQTLCLSUCSAZDY-ATGUSINASA-N Nerolidol Chemical compound CC(C)=CCC\C(C)=C\CC[C@](C)(O)C=C FQTLCLSUCSAZDY-ATGUSINASA-N 0.000 claims 2
- ZYEMGPIYFIJGTP-UHFFFAOYSA-N O-methyleugenol Chemical compound COC1=CC=C(CC=C)C=C1OC ZYEMGPIYFIJGTP-UHFFFAOYSA-N 0.000 claims 2
- 239000005643 Pelargonic acid Substances 0.000 claims 2
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 claims 2
- ZVOLCUVKHLEPEV-UHFFFAOYSA-N Quercetagetin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=C(O)C(O)=C(O)C=C2O1 ZVOLCUVKHLEPEV-UHFFFAOYSA-N 0.000 claims 2
- HWTZYBCRDDUBJY-UHFFFAOYSA-N Rhynchosin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=CC(O)=C(O)C=C2O1 HWTZYBCRDDUBJY-UHFFFAOYSA-N 0.000 claims 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims 2
- 229960000583 acetic acid Drugs 0.000 claims 2
- 229940091181 aconitic acid Drugs 0.000 claims 2
- 239000001361 adipic acid Substances 0.000 claims 2
- 235000011037 adipic acid Nutrition 0.000 claims 2
- 229960000250 adipic acid Drugs 0.000 claims 2
- 235000010443 alginic acid Nutrition 0.000 claims 2
- 229920000615 alginic acid Polymers 0.000 claims 2
- RGZSQWQPBWRIAQ-LSDHHAIUSA-N alpha-Bisabolol Natural products CC(C)=CCC[C@@](C)(O)[C@@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-LSDHHAIUSA-N 0.000 claims 2
- IGODOXYLBBXFDW-UHFFFAOYSA-N alpha-Terpinyl acetate Chemical compound CC(=O)OC(C)(C)C1CCC(C)=CC1 IGODOXYLBBXFDW-UHFFFAOYSA-N 0.000 claims 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims 2
- XPNGNIFUDRPBFJ-UHFFFAOYSA-N alpha-methylbenzylalcohol Natural products CC1=CC=CC=C1CO XPNGNIFUDRPBFJ-UHFFFAOYSA-N 0.000 claims 2
- 239000003443 antiviral agent Substances 0.000 claims 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims 2
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 claims 2
- GWYFCOCPABKNJV-UHFFFAOYSA-N beta-methyl-butyric acid Natural products CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 claims 2
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 claims 2
- 229940116229 borneol Drugs 0.000 claims 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 claims 2
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 claims 2
- 239000001639 calcium acetate Substances 0.000 claims 2
- 229960005147 calcium acetate Drugs 0.000 claims 2
- 235000011092 calcium acetate Nutrition 0.000 claims 2
- 229930008380 camphor Natural products 0.000 claims 2
- 229960000846 camphor Drugs 0.000 claims 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims 2
- 229960000541 cetyl alcohol Drugs 0.000 claims 2
- 239000003638 chemical reducing agent Substances 0.000 claims 2
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- 239000007789 gas Substances 0.000 claims 1
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- 235000021472 generally recognized as safe Nutrition 0.000 claims 1
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 claims 1
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 claims 1
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 claims 1
- 235000011187 glycerol Nutrition 0.000 claims 1
- 230000003054 hormonal effect Effects 0.000 claims 1
- 235000001050 hortel pimenta Nutrition 0.000 claims 1
- 229960004337 hydroquinone Drugs 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- 230000007813 immunodeficiency Effects 0.000 claims 1
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- 238000001802 infusion Methods 0.000 claims 1
- 239000007924 injection Substances 0.000 claims 1
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- 238000007918 intramuscular administration Methods 0.000 claims 1
- 238000007912 intraperitoneal administration Methods 0.000 claims 1
- 238000001990 intravenous administration Methods 0.000 claims 1
- 229940117955 isoamyl acetate Drugs 0.000 claims 1
- WYXXLXHHWYNKJF-UHFFFAOYSA-N isocarvacrol Natural products CC(C)C1=CC=C(O)C(C)=C1 WYXXLXHHWYNKJF-UHFFFAOYSA-N 0.000 claims 1
- 150000003893 lactate salts Chemical class 0.000 claims 1
- 229940089454 lauryl aldehyde Drugs 0.000 claims 1
- 239000001102 lavandula vera Substances 0.000 claims 1
- 235000018219 lavender Nutrition 0.000 claims 1
- 229920005610 lignin Polymers 0.000 claims 1
- 239000004571 lime Substances 0.000 claims 1
- 235000001510 limonene Nutrition 0.000 claims 1
- 229940087305 limonene Drugs 0.000 claims 1
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 229940116837 methyleugenol Drugs 0.000 claims 1
- PRHTXAOWJQTLBO-UHFFFAOYSA-N methyleugenol Natural products COC1=CC=C(C(C)=C)C=C1OC PRHTXAOWJQTLBO-UHFFFAOYSA-N 0.000 claims 1
- 206010027599 migraine Diseases 0.000 claims 1
- 235000010460 mustard Nutrition 0.000 claims 1
- 239000001702 nutmeg Substances 0.000 claims 1
- YLYBTZIQSIBWLI-UHFFFAOYSA-N octyl acetate Chemical group CCCCCCCCOC(C)=O YLYBTZIQSIBWLI-UHFFFAOYSA-N 0.000 claims 1
- 239000002674 ointment Substances 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims 1
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 claims 1
- 150000002989 phenols Chemical class 0.000 claims 1
- 229940100595 phenylacetaldehyde Drugs 0.000 claims 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 claims 1
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- SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 claims 1
- 150000008442 polyphenolic compounds Chemical class 0.000 claims 1
- 229960004109 potassium acetate Drugs 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 208000020016 psychiatric disease Diseases 0.000 claims 1
- 229940079877 pyrogallol Drugs 0.000 claims 1
- 239000012492 regenerant Substances 0.000 claims 1
- 229960001755 resorcinol Drugs 0.000 claims 1
- 239000000377 silicon dioxide Substances 0.000 claims 1
- 208000019116 sleep disease Diseases 0.000 claims 1
- 229960004249 sodium acetate Drugs 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 239000007921 spray Substances 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- 230000001954 sterilising effect Effects 0.000 claims 1
- 238000007920 subcutaneous administration Methods 0.000 claims 1
- 239000000829 suppository Substances 0.000 claims 1
- 239000003826 tablet Substances 0.000 claims 1
- 229960000790 thymol Drugs 0.000 claims 1
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- 229940004858 usnic acid Drugs 0.000 claims 1
- ICTZCAHDGHPRQR-UHFFFAOYSA-N usnic acid Natural products OC1=C(C)C(O)=C(C(C)=O)C2=C1C1(C)C(O)=C(C(=O)C)C(=O)C=C1O2 ICTZCAHDGHPRQR-UHFFFAOYSA-N 0.000 claims 1
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP00124497 | 2000-11-09 | ||
| PCT/EP2001/012974 WO2002038181A2 (de) | 2000-11-09 | 2001-11-09 | Synergistisches, aromastoffhaltiges arzneimittel mit antagonistischer, regenerativer und/oder protagonistischer dekontaminativer wirkung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004513153A JP2004513153A (ja) | 2004-04-30 |
| JP2004513153A5 true JP2004513153A5 (enExample) | 2005-05-19 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2002540763A Pending JP2004513153A (ja) | 2000-11-09 | 2001-11-09 | Ｇｒａｓ香料またはその誘導体を含む殺菌性組成物を含有する薬物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20050014827A1 (enExample) |
| EP (1) | EP1331946A2 (enExample) |
| JP (1) | JP2004513153A (enExample) |
| AU (2) | AU2002227913B2 (enExample) |
| CA (1) | CA2428318A1 (enExample) |
| WO (1) | WO2002038181A2 (enExample) |
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|---|---|---|---|---|
| US20040241258A1 (en) * | 2003-05-28 | 2004-12-02 | Mentkow Jack W. | Insect repellent for humans and animals |
| WO2006092151A1 (en) * | 2005-03-01 | 2006-09-08 | Mohamed Zakaria Ahmed El Masri | Topical corticosteroid containing formulation for treatment of psoriasis, eczema, ulcer and burns |
| WO2006120495A1 (fr) * | 2005-05-13 | 2006-11-16 | Advanced Scientific Developements | Composition pharmaceutique comprenant un antiviral, an antitumoral ou un antiparasitaire, et un actif choisi parmi le carveol, le thymol, l’eugenol, le borneol et le carvacrol |
| JP2012072179A (ja) * | 2005-08-30 | 2012-04-12 | Kao Corp | バイオフィルム抑制剤 |
| US20090312279A1 (en) * | 2005-12-23 | 2009-12-17 | Sterilex Technologies, Llc | Antimicrobial compositions |
| US20080194518A1 (en) * | 2005-12-23 | 2008-08-14 | MOOKERJEE Pradip | Antimicrobial Compositions |
| US20070258996A1 (en) * | 2005-12-23 | 2007-11-08 | The Sterilex Corporation | Antimicrobial compositions |
| KR101384328B1 (ko) | 2006-03-23 | 2014-04-10 | 가오 가부시키가이샤 | 세균막 형성 억제제 조성물 |
| CN101448399B (zh) * | 2006-04-21 | 2013-06-05 | 花王株式会社 | 生物膜控制剂组合物 |
| FR2908660B1 (fr) * | 2006-11-17 | 2013-02-08 | Gombert Bernard Lucien | Composition terpenique anti-microorganisme |
| US20080213440A1 (en) * | 2007-03-01 | 2008-09-04 | Cadbury Adams Usa Llc | Non-Aldehyde Cinnamon Flavor and Delivery Systems Therefor |
| US20080253976A1 (en) * | 2007-04-16 | 2008-10-16 | Douglas Craig Scott | Personal Care Compositions Comprising An Antimicrobial Blend of Essential Oils or Constituents Thereof |
| ITMI20071623A1 (it) * | 2007-08-03 | 2009-02-04 | Vetagro S R L | Composizione sinergica comprendente sostanze aromatizzanti ed acidi organici, e relativo uso |
| ES2535119T3 (es) * | 2007-09-11 | 2015-05-05 | Dsm Ip Assets B.V. | Uso de sesquiterpenos como aditivos de piensos en alimentación animal |
| EP2237684A2 (en) | 2008-01-08 | 2010-10-13 | Akthelia Pharmaceuticals | Agonists for antimicrobial peptide systems |
| EP2135512B1 (de) | 2008-06-19 | 2010-06-16 | Ali Dr. Muin | Zusammensetzung auf der Basis von Äpfelsäure, Kaffeesäure, einem Flavan-3-ol und einem Anthocyan und ihre Verwendung in Lebensmitteln und Medizin |
| JO3416B1 (ar) | 2009-04-27 | 2019-10-20 | Jeneil Biosurfactant Co Llc | تركيبات مضادة للبكتيريا وطرق استخدامها |
| FR2946255B1 (fr) * | 2009-06-05 | 2013-05-24 | Natepharm | Composition comprenant du trans-cinnamaldehyde |
| US9968564B2 (en) * | 2009-06-05 | 2018-05-15 | Intercontinental Great Brands Llc | Delivery of functional compounds |
| US8859003B2 (en) * | 2009-06-05 | 2014-10-14 | Intercontinental Great Brands Llc | Preparation of an enteric release system |
| US20100310726A1 (en) * | 2009-06-05 | 2010-12-09 | Kraft Foods Global Brands Llc | Novel Preparation of an Enteric Release System |
| US20100307542A1 (en) * | 2009-06-05 | 2010-12-09 | Kraft Foods Global Brands Llc | Method of Reducing Surface Oil on Encapsulated Material |
| GB2473460B (en) * | 2009-09-10 | 2016-02-10 | Univ Surrey | Antimicrobial Composition |
| JP2013506650A (ja) * | 2009-10-02 | 2013-02-28 | イッスム リサーチ デベロプメント カンパニー オブ ザ ヘブライ ユニバーシティ オブ エルサレム リミテッド | サニタイジング組成物 |
| US20120003162A1 (en) | 2010-06-30 | 2012-01-05 | Mcneil-Ppc, Inc. | Methods of Preparing Non-Alcohol Bioactive Esential Oil Mouth Rinses |
| US9084902B2 (en) | 2010-06-30 | 2015-07-21 | Mcneil-Ppc, Inc. | Non-alchohol bioactive essential oil mouth rinses |
| CA2771980C (en) | 2010-08-27 | 2014-05-13 | Anitox Corporation | Antimicrobial formulation |
| DE102011077055A1 (de) * | 2011-06-07 | 2012-12-13 | Beiersdorf Ag | Wirkstoffkombinationen aus å-Polylysin (Epsilon-Polylysin) und einem oder mehreren aromatischen Estern |
| RU2014115606A (ru) | 2011-10-20 | 2015-11-27 | Анитокс Корпорейшн | Антимикробные композиции, содержащие пеларгоновую кислоту |
| US9693941B2 (en) | 2011-11-03 | 2017-07-04 | Conopco, Inc. | Liquid personal wash composition |
| EP2787823B2 (en) | 2011-12-06 | 2019-10-30 | Unilever N.V. | Antimicrobial composition |
| MX345634B (es) * | 2011-12-06 | 2017-02-08 | Unilever Nv | Composicion microbicida. |
| CN104080340B (zh) | 2011-12-06 | 2018-05-29 | 荷兰联合利华有限公司 | 抗微生物组合物 |
| EP2787822B1 (en) | 2011-12-06 | 2017-02-08 | Unilever N.V. | Microbicidal composition |
| MX355433B (es) | 2011-12-06 | 2018-04-18 | Unilever Nv | Composicion microbicida. |
| CN104010513B (zh) | 2011-12-06 | 2018-04-24 | 荷兰联合利华有限公司 | 杀微生物组合物 |
| CN110637816B (zh) | 2011-12-06 | 2021-04-27 | 荷兰联合利华有限公司 | 杀微生物组合物 |
| EP2787828B1 (en) | 2011-12-06 | 2016-09-07 | Unilever N.V. | Antimicrobial composition |
| WO2013083590A1 (en) | 2011-12-06 | 2013-06-13 | Unilever N.V. | Method for disinfecting a surface |
| US8859005B2 (en) | 2012-12-03 | 2014-10-14 | Intercontinental Great Brands Llc | Enteric delivery of functional ingredients suitable for hot comestible applications |
| MY190687A (en) * | 2013-03-15 | 2022-05-11 | Jeneil Biosurfactant Co Llc | Antimicrobial compositions and related methods of use |
| CA2955981C (en) * | 2014-07-22 | 2022-10-25 | Ralco Nutrition, Inc. | Antiviral compositions comprising one or more essential oils |
| KR101676356B1 (ko) | 2014-07-23 | 2016-11-29 | 주식회사 대호 | 사료용 곰팡이 성장 억제제 및 그 제조 방법 |
| CN104225534A (zh) * | 2014-09-10 | 2014-12-24 | 吕赛林 | 一种治疗腰肩脚风湿病膏药及其制备方法 |
| CN104873625A (zh) * | 2015-05-28 | 2015-09-02 | 李�杰 | 治疗夜啼症的膏药 |
| CN107183070B (zh) * | 2017-07-13 | 2020-07-28 | 临沂市农业科学院 | 一种防治植物炭疽病的植物源农药及其应用 |
| JPWO2019087883A1 (ja) * | 2017-10-31 | 2020-11-26 | 富士フイルム株式会社 | 抗ウイルス用組成物、抗ノロウイルス用組成物、スプレー、ワイパー |
| JP7520715B2 (ja) * | 2018-03-20 | 2024-07-23 | フイルメニツヒ ソシエテ アノニム | 抗菌組成物 |
| WO2021155143A1 (en) | 2020-01-31 | 2021-08-05 | Jeneil Biosurfactant Company, Llc | Antimicrobial compositions for modulation of fruit and vegetable tissue necrosis |
| JP2021195348A (ja) * | 2020-06-17 | 2021-12-27 | 大日本除蟲菊株式会社 | 防カビ剤、カビ臭発生抑制組成物、及びカビ臭消臭組成物。 |
| CN112472693B (zh) * | 2020-11-30 | 2022-04-01 | 汕头大学 | 一种体型结构的植物单宁抗菌剂及其制备方法和应用 |
| CN112868928B (zh) * | 2021-02-09 | 2022-04-22 | 中国农业大学 | 香味剂在调节母猪肠道微生物和提高繁殖性能中的应用 |
| CN117119884A (zh) * | 2021-04-15 | 2023-11-24 | 花王株式会社 | 液体喷雾用病毒灭活组合物 |
| WO2022220290A1 (ja) * | 2021-04-15 | 2022-10-20 | 花王株式会社 | 液噴霧用ウイルス不活化組成物 |
| JP2023063147A (ja) * | 2021-10-22 | 2023-05-09 | 花王株式会社 | ウイルス不活化剤 |
| JP2023063142A (ja) * | 2021-10-22 | 2023-05-09 | 花王株式会社 | ウイルス不活化剤 |
| JP2023063143A (ja) * | 2021-10-22 | 2023-05-09 | 花王株式会社 | ウイルス不活化剤 |
| JP7765245B2 (ja) * | 2021-10-22 | 2025-11-06 | 花王株式会社 | ウイルス不活化剤 |
| JP2023063141A (ja) * | 2021-10-22 | 2023-05-09 | 花王株式会社 | ウイルス不活化剤 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1772975A (en) * | 1925-06-20 | 1930-08-12 | Firm C H Boehringer Sohn Chem | Process for the production of antiseptic agents |
| US4200655A (en) * | 1978-08-15 | 1980-04-29 | Sterling Drug Inc. | Benzyl alcohol virucidal process |
| DE3382087D1 (de) * | 1982-09-17 | 1991-02-07 | Human Oltoanyagtermelo | Praeparate zur behandlung von wunden der hautoberflaeche und verfahren zur herstellung derartiger praeparate. |
| ES2173274T3 (es) * | 1995-03-31 | 2002-10-16 | Jorg-Peter Prof Schur | Procedimiento para mejorar la conservabilidad y/o para la estabilizacion de productos perecederos por microbios. |
| DE19726429A1 (de) * | 1997-06-23 | 1998-12-24 | Schuer Joerg Peter Prof | Verfahren und Additiv zur Haltbarkeitsverbesserung und/oder Stabilisierung von mikrobiell verderblichen Produkten |
| US20020176882A1 (en) * | 1997-06-23 | 2002-11-28 | Schur Jorg Peter | Additive the improvement and/or stabilization of the keeping quality of microbially perishable products |
| ES2252956T3 (es) * | 1998-07-13 | 2006-05-16 | Joerg Peter Schuer | Composicion antimicrobiana. |
| EP1138772A4 (en) * | 1998-12-11 | 2005-04-06 | Takeda Chemical Industries Ltd | PROCESS FOR THE PRODUCTION OF APELINE |
| EP1038782A1 (en) * | 1999-03-22 | 2000-09-27 | The Procter & Gamble Company | In line production of solid objects |
-
2001
- 2001-11-09 JP JP2002540763A patent/JP2004513153A/ja active Pending
- 2001-11-09 EP EP01989449A patent/EP1331946A2/de not_active Withdrawn
- 2001-11-09 AU AU2002227913A patent/AU2002227913B2/en not_active Ceased
- 2001-11-09 AU AU2791302A patent/AU2791302A/xx active Pending
- 2001-11-09 CA CA002428318A patent/CA2428318A1/en not_active Abandoned
- 2001-11-09 WO PCT/EP2001/012974 patent/WO2002038181A2/de not_active Ceased
- 2001-11-09 US US10/416,479 patent/US20050014827A1/en not_active Abandoned
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