TW307758B - - Google Patents
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- TW307758B TW307758B TW084107225A TW84107225A TW307758B TW 307758 B TW307758 B TW 307758B TW 084107225 A TW084107225 A TW 084107225A TW 84107225 A TW84107225 A TW 84107225A TW 307758 B TW307758 B TW 307758B
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- 239000000203 mixture Substances 0.000 claims abstract description 96
- 150000001875 compounds Chemical class 0.000 claims abstract description 73
- 238000000034 method Methods 0.000 claims abstract description 24
- 229940126062 Compound A Drugs 0.000 claims abstract description 17
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims abstract description 17
- 230000000855 fungicidal effect Effects 0.000 claims abstract description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000011737 fluorine Substances 0.000 claims abstract description 3
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 3
- -1 methyl Chemical group 0.000 claims description 50
- 238000011049 filling Methods 0.000 claims description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
- 239000007788 liquid Substances 0.000 claims description 28
- 230000003449 preventive effect Effects 0.000 claims description 27
- 230000000844 anti-bacterial effect Effects 0.000 claims description 19
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical group CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 15
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 15
- 239000004094 surface-active agent Substances 0.000 claims description 14
- 239000007787 solid Substances 0.000 claims description 13
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
- 239000005761 Dimethomorph Substances 0.000 claims description 10
- QNBTYORWCCMPQP-JXAWBTAJSA-N (Z)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C/C(=O)N1CCOCC1 QNBTYORWCCMPQP-JXAWBTAJSA-N 0.000 claims description 9
- 239000007789 gas Substances 0.000 claims description 8
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 claims description 8
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 claims description 7
- VVTUYOFCBKGBIP-UHFFFAOYSA-L P([O-])([O-])=O.C(C)[Al+2] Chemical group P([O-])([O-])=O.C(C)[Al+2] VVTUYOFCBKGBIP-UHFFFAOYSA-L 0.000 claims description 7
- 239000005839 Tebuconazole Substances 0.000 claims description 7
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 7
- 239000011701 zinc Substances 0.000 claims description 7
- 229910052725 zinc Inorganic materials 0.000 claims description 7
- 239000004480 active ingredient Substances 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- 229910052708 sodium Inorganic materials 0.000 claims description 5
- 239000005780 Fluazinam Substances 0.000 claims description 4
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000004434 sulfur atom Chemical group 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
- 201000003984 candidiasis Diseases 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 230000001717 pathogenic effect Effects 0.000 claims description 3
- 239000005747 Chlorothalonil Substances 0.000 claims description 2
- 239000005781 Fludioxonil Substances 0.000 claims description 2
- XFOXDUJCOHBXRC-UHFFFAOYSA-N N-Ethyl-N-methyl-4-(trifluoromethyl)-2-(3,4-dimethoxyphenyl)benzamide Chemical compound CCN(C)C(=O)C1=CC=C(C(F)(F)F)C=C1C1=CC=C(OC)C(OC)=C1 XFOXDUJCOHBXRC-UHFFFAOYSA-N 0.000 claims description 2
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims description 2
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 claims description 2
- 230000001225 therapeutic effect Effects 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 claims description 2
- VJKNHZZAUKVOBT-UHFFFAOYSA-N CC(NC(S)=S)NC(S)=S Chemical group CC(NC(S)=S)NC(S)=S VJKNHZZAUKVOBT-UHFFFAOYSA-N 0.000 claims 3
- WEJHBEDHLLBJFW-UHFFFAOYSA-N 4-(trifluoromethyl)benzamide Chemical compound NC(=O)C1=CC=C(C(F)(F)F)C=C1 WEJHBEDHLLBJFW-UHFFFAOYSA-N 0.000 claims 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 2
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 claims 1
- GTKIGDZXPDCIKR-UHFFFAOYSA-N 2-phenylbenzamide Chemical class NC(=O)C1=CC=CC=C1C1=CC=CC=C1 GTKIGDZXPDCIKR-UHFFFAOYSA-N 0.000 claims 1
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 claims 1
- 239000005750 Copper hydroxide Substances 0.000 claims 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims 1
- 239000005751 Copper oxide Substances 0.000 claims 1
- 239000005756 Cymoxanil Substances 0.000 claims 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims 1
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- JKXUNWLKMLTMBJ-UHFFFAOYSA-N carbamodithioic acid;manganese Chemical compound [Mn].NC(S)=S.NC(S)=S JKXUNWLKMLTMBJ-UHFFFAOYSA-N 0.000 claims 1
- 229910001956 copper hydroxide Inorganic materials 0.000 claims 1
- 229910000431 copper oxide Inorganic materials 0.000 claims 1
- 125000005805 dimethoxy phenyl group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 229910052748 manganese Inorganic materials 0.000 claims 1
- 239000011572 manganese Substances 0.000 claims 1
- WJZHMLNIAZSFDO-UHFFFAOYSA-N manganese zinc Chemical group [Mn].[Zn] WJZHMLNIAZSFDO-UHFFFAOYSA-N 0.000 claims 1
- 231100000252 nontoxic Toxicity 0.000 claims 1
- 230000003000 nontoxic effect Effects 0.000 claims 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 1
- 210000004916 vomit Anatomy 0.000 claims 1
- 230000008673 vomiting Effects 0.000 claims 1
- 241000233866 Fungi Species 0.000 abstract description 6
- 229910052760 oxygen Inorganic materials 0.000 abstract description 2
- 239000001301 oxygen Substances 0.000 abstract description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 230000003032 phytopathogenic effect Effects 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 47
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- 201000010099 disease Diseases 0.000 description 39
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- 239000000725 suspension Substances 0.000 description 32
- 239000013543 active substance Substances 0.000 description 29
- 239000000843 powder Substances 0.000 description 24
- 240000003768 Solanum lycopersicum Species 0.000 description 20
- 241000233622 Phytophthora infestans Species 0.000 description 19
- 241000607479 Yersinia pestis Species 0.000 description 17
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- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 15
- 241000209140 Triticum Species 0.000 description 15
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 12
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- 235000021307 Triticum Nutrition 0.000 description 11
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- 239000000047 product Substances 0.000 description 11
- 239000002253 acid Substances 0.000 description 10
- 238000001727 in vivo Methods 0.000 description 10
- 239000002245 particle Substances 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 241000897276 Termes Species 0.000 description 9
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- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 9
- 239000007921 spray Substances 0.000 description 9
- 239000005822 Propiconazole Substances 0.000 description 8
- 239000008187 granular material Substances 0.000 description 8
- 240000006365 Vitis vinifera Species 0.000 description 7
- 235000014787 Vitis vinifera Nutrition 0.000 description 7
- 239000002270 dispersing agent Substances 0.000 description 7
- 239000000945 filler Substances 0.000 description 7
- 241000238631 Hexapoda Species 0.000 description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 6
- 230000002079 cooperative effect Effects 0.000 description 6
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- 239000000839 emulsion Substances 0.000 description 6
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 6
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 5
- 244000061456 Solanum tuberosum Species 0.000 description 5
- 230000000875 corresponding effect Effects 0.000 description 5
- 235000019441 ethanol Nutrition 0.000 description 5
- 208000015181 infectious disease Diseases 0.000 description 5
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- ZMYFCFLJBGAQRS-IAGOWNOFSA-N (2S,3R)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@]1(CN2N=CN=C2)[C@@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IAGOWNOFSA-N 0.000 description 4
- LSBDFXRDZJMBSC-UHFFFAOYSA-N 2-phenylacetamide Chemical compound NC(=O)CC1=CC=CC=C1 LSBDFXRDZJMBSC-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
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- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 4
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- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 3
- 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
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- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 229910052704 radon Inorganic materials 0.000 description 3
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- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 3
- DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 3
- AFINAILKDBCXMX-PBHICJAKSA-N (2s,3r)-2-amino-3-hydroxy-n-(4-octylphenyl)butanamide Chemical compound CCCCCCCCC1=CC=C(NC(=O)[C@@H](N)[C@@H](C)O)C=C1 AFINAILKDBCXMX-PBHICJAKSA-N 0.000 description 2
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 description 2
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- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 2
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- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
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- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 description 2
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- LMVPQMGRYSRMIW-KRWDZBQOSA-N fenamidone Chemical compound O=C([C@@](C)(N=C1SC)C=2C=CC=CC=2)N1NC1=CC=CC=C1 LMVPQMGRYSRMIW-KRWDZBQOSA-N 0.000 description 2
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
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- GTWJETSWSUWSEJ-UHFFFAOYSA-N n-benzylaniline Chemical class C=1C=CC=CC=1CNC1=CC=CC=C1 GTWJETSWSUWSEJ-UHFFFAOYSA-N 0.000 description 2
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- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Polymers OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
- CMPQUABWPXYYSH-UHFFFAOYSA-L phenyl phosphate(2-) Polymers [O-]P([O-])(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-L 0.000 description 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
- 229940067157 phenylhydrazine Drugs 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- OLBCVFGFOZPWHH-UHFFFAOYSA-N propofol Chemical compound CC(C)C1=CC=CC(C(C)C)=C1O OLBCVFGFOZPWHH-UHFFFAOYSA-N 0.000 description 1
- 229960004134 propofol Drugs 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 235000001508 sulfur Nutrition 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- QERYCTSHXKAMIS-UHFFFAOYSA-N thiophene-2-carboxylic acid Chemical compound OC(=O)C1=CC=CS1 QERYCTSHXKAMIS-UHFFFAOYSA-N 0.000 description 1
- YJVLWFXZVBOFRZ-UHFFFAOYSA-N titanium zinc Chemical compound [Ti].[Zn] YJVLWFXZVBOFRZ-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- ABDKAPXRBAPSQN-UHFFFAOYSA-N veratrole Chemical group COC1=CC=CC=C1OC ABDKAPXRBAPSQN-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9409331A FR2722652B1 (fr) | 1994-07-22 | 1994-07-22 | Composition fongicide comprenant une 2-imidazoline-5-one |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW307758B true TW307758B (cg-RX-API-DMAC7.html) | 1997-06-11 |
Family
ID=9465821
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW084107225A TW307758B (cg-RX-API-DMAC7.html) | 1994-07-22 | 1995-07-12 |
Country Status (34)
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2751845B1 (fr) * | 1996-07-30 | 1998-09-11 | Rhone Poulenc Agrochimie | Nouvelle composition fongicide comprenant une 2-imidazoline- 5-one |
| AU6040398A (en) * | 1997-01-30 | 1998-08-25 | E.I. Du Pont De Nemours And Company | Fungicidal compositions |
| CA2280809C (en) * | 1997-03-05 | 2007-04-24 | Novartis Ag | Fungicidal compositions based on metalyxyl |
| CN1049788C (zh) * | 1997-07-20 | 2000-02-23 | ็ไฟฃไบบ | ไธคๅฃฐ้ไธ็ปด็ซไฝๅฃฐๅค็ๅจ |
| GB9718366D0 (en) | 1997-08-29 | 1997-11-05 | Ciba Geigy Ag | Novel combinations |
| JP4522504B2 (ja) * | 1997-12-01 | 2010-08-11 | ็ณๅ็ฃๆฅญๆ ชๅผไผ็คพ | ๆๅฎณ็็ฉ้ฒ้ค็จ็ตๆ็ฉใใใณๆๅฎณ็็ฉใฎ้ฒ้คๆนๆณ |
| UA61064C2 (uk) * | 1997-12-02 | 2003-11-17 | ะ ะพะฝ-ะัะปะตะฝะบ ะะณัะพ | ะกะธะฝะตัะณััะฝะฐ ััะฝะณััะธะดะฝะฐ ะบะพะผะฟะพะทะธััั, ัะพ ะผัััะธัั 2-ัะฝัะดะฐะทะพะปัะฝ-5-ะพะฝ ัะฐ ัะฟะพััะฑ ะฑะพัะพััะฑะธ ะท ัััะพะฟะฐัะพะณะตะฝะฝะธะผะธ ะณัะธะฑะบะฐะผะธ ะบัะปัััั |
| FR2771898B1 (fr) * | 1997-12-04 | 2000-01-07 | Rhone Poulenc Agrochimie | Composition fongicide et/ou bactericide synergique |
| PL191333B1 (pl) * | 1997-12-18 | 2006-04-28 | Basf Ag | Mieszanina grzybobรณjcza |
| AP990A (en) | 1997-12-30 | 2001-08-02 | Rhone Poulenc Agrochimie | Novel fungicidal composition comprising A 2-imidazolin-5-one. |
| CN1126450C (zh) * | 1997-12-30 | 2003-11-05 | ็ฝ็บณ-ๆฎๆๅ ๅไธๅๅญฆๅ ฌๅธ | ๅซๆ2๏ผๅชๅๅ๏ผ5๏ผ้ ฎ็ๆฐ็ๆ็่ๅ็ปๅ็ฉ |
| WO1999053761A1 (fr) * | 1998-04-16 | 1999-10-28 | Aventis Cropscience S.A. | Nouvelle utilisation de composes antifongiques et/ou antibacteriens et/ou antiviraux |
| UA70327C2 (uk) * | 1998-06-08 | 2004-10-15 | ะะฐัั ะะบััะตะฝะณะตะทะตะปััะฐัั | ะกะฟะพััะฑ ะฑะพัะพััะฑะธ ะท ัััะพะฟะฐัะพะณะตะฝะฝะธะผะธ ั ะฒะพัะพะฑะฐะผะธ ััะปัััะบะพะณะพัะฟะพะดะฐัััะบะธั ัะพัะปะธะฝ ัะฐ ััะฝะณััะธะดะฝะฐ ะบะพะผะฟะพะทะธััั |
| GB9819317D0 (en) * | 1998-09-04 | 1998-10-28 | Novartis Ag | Organic compounds |
| FR2783401B1 (fr) * | 1998-09-21 | 2000-10-20 | Rhone Poulenc Agrochimie | Nouvelles compositions fongicides |
| DE19904081A1 (de) * | 1999-02-02 | 2000-08-03 | Bayer Ag | Fungizide Wirkstoffkombinationen |
| FR2789551B1 (fr) | 1999-02-12 | 2002-06-21 | Aventis Cropscience Sa | Compositions fongicides pour la protection des fruits |
| JP4351789B2 (ja) | 1999-07-16 | 2009-10-28 | ็ณๅ็ฃๆฅญๆ ชๅผไผ็คพ | ๆๅฎณ็็ฉ้ฒ้ค็จ็ตๆ็ฉใใใณๆๅฎณ็็ฉใฎ้ฒ้คๆนๆณ |
| FR2821718B1 (fr) * | 2001-03-08 | 2003-06-13 | Aventis Cropscience Sa | Nouvelles compositions fongicides a base de derives de pyridylmethylbenzamide et d'imidazoline ou d'oxazolidine |
| FR2831768B1 (fr) * | 2001-11-08 | 2004-10-29 | Aventis Cropscience Sa | Composition fongicide comprenant au moins un compose fongici de de la famille des anilinopyrimidines et au moins un derive de l'acide phosphoreux et utilisation de cette composition pour la lutte contre les maladies des plantes |
| ITMI20012430A1 (it) * | 2001-11-19 | 2003-05-19 | Isagro Spa | Composizioni a base di sali rameici sali rameici e loro utilizzo per il controllo di fitopatogeni |
| TW200306155A (en) * | 2002-03-19 | 2003-11-16 | Du Pont | Benzamides and advantageous compositions thereof for use as fungicides |
| JP4399622B2 (ja) * | 2003-02-20 | 2010-01-20 | ใใคใจใซใฏใญใใใตใคใจใณในๆ ชๅผไผ็คพ | ่พฒๅ่ธ็จๆฎบ่ๅค็ตๆ็ฉ |
| ES2535045T3 (es) * | 2003-04-10 | 2015-05-04 | Vanderbilt Royalty Sub L.P. | Usos y composiciones para administraciรณn de capsaicina |
| WO2007092580A2 (en) * | 2006-02-08 | 2007-08-16 | Phibro-Tech Inc. | Biocidal azole emulsion concentrates having high active ingredient content |
| WO2008069822A1 (en) * | 2006-02-21 | 2008-06-12 | Phibro-Tech Inc. | Biocidal azole emulsion concentrates having high active ingredient content |
| GB2456752B (en) * | 2007-12-19 | 2012-09-19 | Rotam Agrochem Int Co Ltd | Agrochemical composition and method for preparing the same |
| CN101524078B (zh) * | 2009-01-16 | 2012-05-23 | ้่ฅฟ้ฆๅฐๅฅไฝ็ฉไฟๆคๆ้ๅ ฌๅธ | ไธ็งๆๅ้ไธๅผ่่ฒๅค้ ็ๆ่็ปๅ็ฉ |
| JP5997931B2 (ja) | 2011-05-25 | 2016-09-28 | ็ณๅ็ฃๆฅญๆ ชๅผไผ็คพ | ่พฒๅ่ธ็จๆฎบ่ๅค็ตๆ็ฉๅใณๆค็ฉ็ ๅฎณใฎ้ฒ้คๆนๆณ |
| CN103081915A (zh) * | 2011-11-07 | 2013-05-08 | ๆทฑๅณ่ฏบๆฎไฟกๅๅ่กไปฝๆ้ๅ ฌๅธ | ไธ็งๆ่็ปๅ็ฉ |
| EP2622961A1 (en) | 2012-02-02 | 2013-08-07 | Bayer CropScience AG | Acive compound combinations |
| KR20150013595A (ko) * | 2012-05-09 | 2015-02-05 | ๋๋ฝ์๋ค ๊ฐ๋ถ์ํค๊ฐ์ด์ค | ์๊ฐ ์ฃผ์ ์ |
| CN103444744A (zh) * | 2012-06-02 | 2013-12-18 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๅซๅชๅ่้ ฎไธ็ฒๆฐงๅบไธ็ฏ้ ธ้ ฏ็ฑป็ๆ่็ปๅ็ฉ |
| CN103444738B (zh) * | 2012-06-05 | 2016-06-08 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๅซๅชๅ่้ ฎไธ็กซไปฃๆฐจๅบ็ฒ้ ธ้ ฏ็ฑป็ๆ่็ปๅ็ฉ |
| CN103461338A (zh) * | 2012-06-07 | 2013-12-25 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๅซๅชๅ่้ ฎ็ๆ่็ปๅ็ฉ |
| CN103461343A (zh) * | 2012-06-09 | 2013-12-25 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๅซๅชๅ่้ ฎไธไธๅ็ฑป็้ซๆๆ่็ปๅ็ฉ |
| CN106259347A (zh) * | 2012-06-14 | 2017-01-04 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๅซๅชๅ่้ ฎ็ๆ่็ปๅ็ฉ |
| CN106259350A (zh) * | 2012-06-16 | 2017-01-04 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๅซๅชๅ่้ ฎ็ๆ่็ปๅ็ฉ |
| CN105900991A (zh) * | 2012-06-18 | 2016-08-31 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๅซๅชๅ่้ ฎ็ๆ่็ปๅ็ฉ |
| CN105815319A (zh) * | 2012-06-21 | 2016-08-03 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๅซๅชๅ่้ ฎไธไธๅ็ฑป็้ซๆๆ่็ปๅ็ฉ |
| CN105265439A (zh) * | 2014-07-02 | 2016-01-27 | ๆฑ่้พ็ฏๅๅญฆๆ้ๅ ฌๅธ | ไธ็ง้ฒ้คๆค็ฉ่ ้่็ๆนๆณ |
| CN104186521A (zh) * | 2014-08-29 | 2014-12-10 | ๆฑ่็็ปฟ็พๆคไฟๅ่ฏๅฎ้ชๆ้ๅ ฌๅธ | ๅซๆๅชๅ่้ ฎๅๅช้ฒ่บ็ๆ่็ปๅ็ฉๅๅบ็จ |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US33989A (en) * | 1861-12-24 | Improvement it machines for punching boiler-plates | ||
| AU554648B2 (en) * | 1982-05-27 | 1986-08-28 | Sumitomo Chemical Company, Limited | Fungicidal composition comprising |
| USRE33989E (en) * | 1986-07-16 | 1992-07-07 | Basf Aktiengesellschaft | Oxime ethers and fungicides containing these compounds |
| DE3623921A1 (de) * | 1986-07-16 | 1988-01-21 | Basf Ag | Oximether und diese enthaltende fungizide |
| ATE141589T1 (de) * | 1989-05-17 | 1996-09-15 | Shionogi & Co | Alkoxyiminoacetamid-derivate und ihre verwendung als pilztรถtendes mittel |
| FR2685328B1 (fr) * | 1991-12-20 | 1995-12-01 | Rhone Poulenc Agrochimie | Derives de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
| FR2698359B1 (fr) * | 1992-11-25 | 1995-10-27 | Rhone Poulenc Agrochimie | Derives de 2-alkoxy 2-imidazoline-5-ones fongicides. |
| FR2706456B1 (fr) * | 1993-06-18 | 1996-06-28 | Rhone Poulenc Agrochimie | Dรฉrivรฉs optiquement actifs de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
| EP0642502B1 (en) * | 1992-05-22 | 2000-07-12 | E.I. Du Pont De Nemours And Company | Fungicidal imidazolinones |
| FR2694288B1 (fr) * | 1992-06-30 | 1994-09-09 | Rhone Poulenc Agrochimie | Phenylbenzamides fongicides et procรฉdรฉs pour les prรฉparer. |
-
1994
- 1994-07-22 FR FR9409331A patent/FR2722652B1/fr not_active Expired - Fee Related
-
1995
- 1995-07-12 TW TW084107225A patent/TW307758B/zh active
- 1995-07-17 ZA ZA955935A patent/ZA955935B/xx unknown
- 1995-07-18 MA MA23956A patent/MA23617A1/fr unknown
- 1995-07-18 PE PE1995274084A patent/PE8996A1/es not_active IP Right Cessation
- 1995-07-20 HU HU9700195A patent/HU214978B/hu not_active IP Right Cessation
- 1995-07-20 JP JP50551896A patent/JP3911011B2/ja not_active Expired - Fee Related
- 1995-07-20 SK SK86-97A patent/SK283014B6/sk not_active IP Right Cessation
- 1995-07-20 PT PT95926401T patent/PT773720E/pt unknown
- 1995-07-20 WO PCT/FR1995/000972 patent/WO1996003044A1/fr not_active Ceased
- 1995-07-20 DK DK95926401T patent/DK0773720T3/da active
- 1995-07-20 ES ES95926401T patent/ES2153041T3/es not_active Expired - Lifetime
- 1995-07-20 CA CA002192989A patent/CA2192989C/fr not_active Expired - Fee Related
- 1995-07-20 UA UA97020754A patent/UA51628C2/uk unknown
- 1995-07-20 PL PL95318328A patent/PL187164B1/pl unknown
- 1995-07-20 KR KR1019970700483A patent/KR100392825B1/ko not_active Expired - Fee Related
- 1995-07-20 BR BR9508792A patent/BR9508792A/pt not_active IP Right Cessation
- 1995-07-20 NZ NZ290153A patent/NZ290153A/xx not_active IP Right Cessation
- 1995-07-20 AT AT95926401T patent/ATE196977T1/de active
- 1995-07-20 DE DE69519170T patent/DE69519170T2/de not_active Expired - Lifetime
- 1995-07-20 RO RO97-00062A patent/RO114863B1/ro unknown
- 1995-07-20 EP EP95926401A patent/EP0773720B1/fr not_active Expired - Lifetime
- 1995-07-20 EG EG61395A patent/EG20395A/xx active
- 1995-07-20 RU RU97102821/04A patent/RU2153257C2/ru not_active IP Right Cessation
- 1995-07-20 CN CN95194227A patent/CN1092484C/zh not_active Expired - Lifetime
- 1995-07-20 AU AU30805/95A patent/AU700287B2/en not_active Ceased
- 1995-07-20 MX MX9700494A patent/MX9700494A/es unknown
- 1995-07-20 US US08/776,064 patent/US5906986A/en not_active Expired - Lifetime
- 1995-07-20 IL IL11468795A patent/IL114687A/xx not_active IP Right Cessation
- 1995-07-20 CZ CZ1997180A patent/CZ293660B6/cs not_active IP Right Cessation
- 1995-07-21 CO CO95032335A patent/CO4600728A1/es unknown
- 1995-07-21 TR TR95/00891A patent/TR199500891A2/xx unknown
-
1997
- 1997-02-13 BG BG101231A patent/BG63524B1/bg unknown
-
1999
- 1999-01-12 US US09/228,946 patent/US6075042A/en not_active Expired - Lifetime
-
2000
- 2000-04-18 US US09/551,580 patent/US6344472B1/en not_active Expired - Lifetime
- 2000-10-19 GR GR20000401221T patent/GR3034642T3/el unknown
-
2002
- 2002-01-15 US US10/044,911 patent/US6638961B2/en not_active Expired - Lifetime
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