TW307758B - - Google Patents
Download PDFInfo
- Publication number
- 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
- Authority
- TW
- Taiwan
- Prior art keywords
- patent application
- methyl
- compound
- item
- ministry
- Prior art date
Links
- 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
- 241000196324 Embryophyta Species 0.000 description 44
- 238000011282 treatment Methods 0.000 description 44
- 201000010099 disease Diseases 0.000 description 39
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 39
- 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
- 241000221785 Erysiphales Species 0.000 description 15
- 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
- 241000233679 Peronosporaceae Species 0.000 description 11
- 235000021307 Triticum Nutrition 0.000 description 11
- 230000006378 damage Effects 0.000 description 11
- 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
- 239000003795 chemical substances by application Substances 0.000 description 9
- 238000011109 contamination Methods 0.000 description 9
- 238000002474 experimental method Methods 0.000 description 9
- 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
- 230000000694 effects Effects 0.000 description 6
- 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
- 239000004615 ingredient Substances 0.000 description 5
- 239000003595 mist Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- 239000000080 wetting agent Substances 0.000 description 5
- 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
- 241000208292 Solanaceae Species 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 239000007900 aqueous suspension Substances 0.000 description 4
- 239000004495 emulsifiable concentrate Substances 0.000 description 4
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 4
- 238000007667 floating Methods 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 230000002195 synergetic effect Effects 0.000 description 4
- 239000004563 wettable powder Substances 0.000 description 4
- 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
- 244000189548 Chrysanthemum x morifolium Species 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 229920001732 Lignosulfonate Polymers 0.000 description 3
- 241000415582 Puccinia striiformis f. sp. tritici Species 0.000 description 3
- 235000002595 Solanum tuberosum Nutrition 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 235000002532 grape seed extract Nutrition 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 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
- SYUHGPGVQRZVTB-UHFFFAOYSA-N radon atom Chemical compound [Rn] SYUHGPGVQRZVTB-UHFFFAOYSA-N 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 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
- 125000004211 3,5-difluorophenyl group Chemical group [H]C1=C(F)C([H])=C(*)C([H])=C1F 0.000 description 2
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 2
- 241000223600 Alternaria Species 0.000 description 2
- 239000005741 Bromuconazole Substances 0.000 description 2
- 241000222122 Candida albicans Species 0.000 description 2
- 206010007134 Candida infections Diseases 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- 206010061217 Infestation Diseases 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- 241000233614 Phytophthora Species 0.000 description 2
- 241000221300 Puccinia Species 0.000 description 2
- 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
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 241000219094 Vitaceae Species 0.000 description 2
- 239000011149 active material Substances 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000002996 emotional effect Effects 0.000 description 2
- 238000009313 farming Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 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
- 239000012530 fluid Substances 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 235000021021 grapes Nutrition 0.000 description 2
- 150000003949 imides Chemical class 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 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
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- GTWJETSWSUWSEJ-UHFFFAOYSA-N n-benzylaniline Chemical class C=1C=CC=CC=1CNC1=CC=CC=C1 GTWJETSWSUWSEJ-UHFFFAOYSA-N 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 239000002674 ointment Substances 0.000 description 2
- 229940049964 oleate Drugs 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 244000045947 parasite Species 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 210000003625 skull Anatomy 0.000 description 2
- 239000004550 soluble concentrate Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229960005349 sulfur Drugs 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 2
- 239000013008 thixotropic agent Substances 0.000 description 2
- NCPXQVVMIXIKTN-UHFFFAOYSA-N trisodium;phosphite Chemical group [Na+].[Na+].[Na+].[O-]P([O-])[O-] NCPXQVVMIXIKTN-UHFFFAOYSA-N 0.000 description 2
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 description 1
- AVAMIJZYYSHRMH-QBDCYTJBSA-N (2e,4e)-hexa-2,4-dienoic acid;(z)-octadec-9-enoic acid Chemical class C\C=C\C=C\C(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O AVAMIJZYYSHRMH-QBDCYTJBSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 1
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 description 1
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 description 1
- LNUBBKFSESILNF-UHFFFAOYSA-N 1-anilino-2-methylsulfanyl-4-phenyl-4h-imidazol-5-one Chemical compound CSC1=NC(C=2C=CC=CC=2)C(=O)N1NC1=CC=CC=C1 LNUBBKFSESILNF-UHFFFAOYSA-N 0.000 description 1
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 description 1
- TVFWYUWNQVRQRG-UHFFFAOYSA-N 2,3,4-tris(2-phenylethenyl)phenol Polymers C=1C=CC=CC=1C=CC1=C(C=CC=2C=CC=CC=2)C(O)=CC=C1C=CC1=CC=CC=C1 TVFWYUWNQVRQRG-UHFFFAOYSA-N 0.000 description 1
- HFZWRUODUSTPEG-UHFFFAOYSA-N 2,4-dichlorophenol Chemical compound OC1=CC=C(Cl)C=C1Cl HFZWRUODUSTPEG-UHFFFAOYSA-N 0.000 description 1
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
- STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 description 1
- DMAXMXPDVWTIRV-UHFFFAOYSA-N 2-(2-phenylethyl)phenol Chemical class OC1=CC=CC=C1CCC1=CC=CC=C1 DMAXMXPDVWTIRV-UHFFFAOYSA-N 0.000 description 1
- JUAUCEVIIOKNLL-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-N-ethyl-3-methyl-4-(trifluoromethyl)benzamide Chemical group CC=1C(=C(C(=O)NCC)C=CC1C(F)(F)F)C1=CC(=C(C=C1)OC)OC JUAUCEVIIOKNLL-UHFFFAOYSA-N 0.000 description 1
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 description 1
- YKDWNEMXGUPAKP-UHFFFAOYSA-N 2-ethyl-3-phenylphenol Chemical class CCC1=C(O)C=CC=C1C1=CC=CC=C1 YKDWNEMXGUPAKP-UHFFFAOYSA-N 0.000 description 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 1
- SGCSGQGGDRALGC-UHFFFAOYSA-N 2-methoxypropanehydrazide Chemical class COC(C)C(=O)NN SGCSGQGGDRALGC-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- MVVWQJUBOXSUKD-UHFFFAOYSA-N 3,4-diaminothiophene-2-carboxylic acid Chemical compound NC1=CSC(C(O)=O)=C1N MVVWQJUBOXSUKD-UHFFFAOYSA-N 0.000 description 1
- JFUNRFXFBHNUSB-UHFFFAOYSA-N 3-methoxy-2-phenylprop-2-enoic acid Chemical compound COC=C(C(O)=O)C1=CC=CC=C1 JFUNRFXFBHNUSB-UHFFFAOYSA-N 0.000 description 1
- RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 description 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 241001556567 Acanthamoeba polyphaga mimivirus Species 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- 241000208173 Apiaceae Species 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 241000208838 Asteraceae Species 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- 240000007124 Brassica oleracea Species 0.000 description 1
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
- 241000233685 Bremia lactucae Species 0.000 description 1
- XJTQKGUUELYZIG-UHFFFAOYSA-N C(C)P(O)(O)=O.P(O)(O)=O Chemical group C(C)P(O)(O)=O.P(O)(O)=O XJTQKGUUELYZIG-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000238366 Cephalopoda Species 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- 241001417978 Channidae Species 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- 235000007516 Chrysanthemum Nutrition 0.000 description 1
- 235000009604 Chrysanthemum X morifolium Nutrition 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 235000004237 Crocus Nutrition 0.000 description 1
- 241000596148 Crocus Species 0.000 description 1
- 240000001980 Cucurbita pepo Species 0.000 description 1
- 235000009852 Cucurbita pepo Nutrition 0.000 description 1
- 241000219104 Cucurbitaceae Species 0.000 description 1
- 239000005757 Cyproconazole Substances 0.000 description 1
- 239000005947 Dimethoate Substances 0.000 description 1
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005775 Fenbuconazole Substances 0.000 description 1
- 239000005777 Fenpropidin Substances 0.000 description 1
- 239000005778 Fenpropimorph Substances 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 241000218228 Humulus Species 0.000 description 1
- 235000008694 Humulus lupulus Nutrition 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- 235000003228 Lactuca sativa Nutrition 0.000 description 1
- 239000004367 Lipase Substances 0.000 description 1
- 102000004882 Lipase Human genes 0.000 description 1
- 108090001060 Lipase Proteins 0.000 description 1
- 240000004658 Medicago sativa Species 0.000 description 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
- 239000005868 Metconazole Substances 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical class C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
- 241000221960 Neurospora Species 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- VTGNXADCFUDPLG-UHFFFAOYSA-N O(O)O.[Cu] Chemical compound O(O)O.[Cu] VTGNXADCFUDPLG-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- ZCYDTLKUSYRURG-UHFFFAOYSA-K P([O-])([O-])=O.P(=O)([O-])(O)O.[Al+3] Chemical compound P([O-])([O-])=O.P(=O)([O-])(O)O.[Al+3] ZCYDTLKUSYRURG-UHFFFAOYSA-K 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 208000002193 Pain Diseases 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 241000233616 Phytophthora capsici Species 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 241000219050 Polygonaceae Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241001123583 Puccinia striiformis Species 0.000 description 1
- 241001533598 Septoria Species 0.000 description 1
- 241000270295 Serpentes Species 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000005840 Tetraconazole Substances 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 239000005846 Triadimenol Substances 0.000 description 1
- 241000223261 Trichoderma viride Species 0.000 description 1
- ZJMLMBICUVVJDX-UHFFFAOYSA-N Trifenmorph Chemical compound C1COCCN1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 ZJMLMBICUVVJDX-UHFFFAOYSA-N 0.000 description 1
- 239000005859 Triticonazole Substances 0.000 description 1
- 240000000260 Typha latifolia Species 0.000 description 1
- 235000005324 Typha latifolia Nutrition 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- SNBMCKOYSLZGNK-UHFFFAOYSA-N [Li].[Zn].[Zn] Chemical compound [Li].[Zn].[Zn] SNBMCKOYSLZGNK-UHFFFAOYSA-N 0.000 description 1
- PGTXKIZLOWULDJ-UHFFFAOYSA-N [Mg].[Zn] Chemical compound [Mg].[Zn] PGTXKIZLOWULDJ-UHFFFAOYSA-N 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Polymers 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 230000007815 allergy Effects 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 230000002146 bilateral effect Effects 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 238000010170 biological method Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 1
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical class [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000012050 conventional carrier Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 1
- UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- JMXKCYUTURMERF-UHFFFAOYSA-N dodemorph Chemical compound C1C(C)OC(C)CN1C1CCCCCCCCCCC1 JMXKCYUTURMERF-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- ZUKSLMGYYPZZJD-UHFFFAOYSA-N ethenimine Chemical class C=C=N ZUKSLMGYYPZZJD-UHFFFAOYSA-N 0.000 description 1
- ZUNGGJHBMLMRFJ-UHFFFAOYSA-O ethoxy-hydroxy-oxophosphanium Chemical compound CCO[P+](O)=O ZUNGGJHBMLMRFJ-UHFFFAOYSA-O 0.000 description 1
- BBIDBFWZMCTRNP-UHFFFAOYSA-N ethylalumane Chemical group CC[AlH2] BBIDBFWZMCTRNP-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 150000002194 fatty esters Chemical class 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 description 1
- VUERQRKTYBIULR-UHFFFAOYSA-N fosetyl Chemical class CCOP(O)=O VUERQRKTYBIULR-UHFFFAOYSA-N 0.000 description 1
- 244000000004 fungal plant pathogen Species 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- SAOPTAQUONRHEV-UHFFFAOYSA-N gold zinc Chemical compound [Zn].[Au] SAOPTAQUONRHEV-UHFFFAOYSA-N 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 239000002054 inoculum Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000007937 lozenge Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- ADHKQMAZPNPPJA-NSHDSACASA-N methyl (2s)-2-isothiocyanato-2-phenylpropanoate Chemical compound COC(=O)[C@@](C)(N=C=S)C1=CC=CC=C1 ADHKQMAZPNPPJA-NSHDSACASA-N 0.000 description 1
- DWKPPFQULDPWHX-UHFFFAOYSA-N methyl 2-aminopropanoate Chemical compound COC(=O)C(C)N DWKPPFQULDPWHX-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000000250 methylamino group Chemical class [H]N(*)C([H])([H])[H] 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- 229940044652 phenolsulfonate Drugs 0.000 description 1
- 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 (enExample) | 1997-06-11 |
Family
ID=9465821
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW084107225A TW307758B (enExample) | 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 |
| WO1998033382A1 (en) * | 1997-01-30 | 1998-08-06 | E.I. Du Pont De Nemours And Company | Fungicidal compositions |
| KR100487188B1 (ko) * | 1997-03-05 | 2005-05-03 | ์ ์ ํ ํํฐ์ํ์ด์ ์ฆ ์๊ฒ | ๋ฉํ๋ฝ์ค์ ๊ธฐ์ฌ๋ก ํ๋ ์ด์ง๊ท ์ ์กฐ์ฑ๋ฌผ |
| 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 |
| DE59805925D1 (de) * | 1997-12-18 | 2002-11-14 | Basf Ag | Fungizide mischungen auf der basis von pyridincarboxamiden |
| CN1126450C (zh) * | 1997-12-30 | 2003-11-05 | ็ฝ็บณ-ๆฎๆๅ ๅไธๅๅญฆๅ ฌๅธ | ๅซๆ2๏ผๅชๅๅ๏ผ5๏ผ้ ฎ็ๆฐ็ๆ็่ๅ็ปๅ็ฉ |
| PT1003375E (pt) * | 1997-12-30 | 2003-03-31 | Aventis Cropscience Sa | Nova composicao fungicida que compreende uma 2-imidazolina-5-ona |
| HRP20000693B8 (en) * | 1998-04-16 | 2007-06-30 | Aventis Cropscience S.A. | Novel use of antifungal and/or antibacterial and/or antiviral compounds |
| 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 |
| EP1610742B1 (en) * | 2003-04-10 | 2015-01-21 | Neurogesx, Inc. | Uses and compositions for administration of capsaicin |
| 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 |
| EP2850944A4 (en) * | 2012-05-09 | 2016-04-27 | Nippon Soda Co | TRUNK INJECTION |
| 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 |
| CN103503873A (zh) * | 2012-06-16 | 2014-01-15 | ้่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 |
| CN108184855A (zh) * | 2014-07-02 | 2018-06-22 | 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 |
| DE3623921A1 (de) * | 1986-07-16 | 1988-01-21 | Basf Ag | Oximether und diese enthaltende fungizide |
| USRE33989E (en) * | 1986-07-16 | 1992-07-07 | Basf Aktiengesellschaft | Oxime ethers and fungicides containing these compounds |
| DE69029334T2 (de) * | 1989-05-17 | 1997-04-30 | Shionogi Seiyaku Kk | Verfahren zur Herstellung von Alkoxyiminoacetamid-Derivaten und ein Zwischenproduckt dafรผr |
| 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. |
| FR2685328B1 (fr) * | 1991-12-20 | 1995-12-01 | Rhone Poulenc Agrochimie | Derives de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
| ES2149815T3 (es) * | 1992-05-22 | 2000-11-16 | Du Pont | Imidazolinonas fungicidas. |
| 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 KR KR1019970700483A patent/KR100392825B1/ko not_active Expired - Fee Related
- 1995-07-20 JP JP50551896A patent/JP3911011B2/ja not_active Expired - Fee Related
- 1995-07-20 EP EP95926401A patent/EP0773720B1/fr not_active Expired - Lifetime
- 1995-07-20 BR BR9508792A patent/BR9508792A/pt not_active IP Right Cessation
- 1995-07-20 CZ CZ1997180A patent/CZ293660B6/cs not_active IP Right Cessation
- 1995-07-20 RO RO97-00062A patent/RO114863B1/ro unknown
- 1995-07-20 AT AT95926401T patent/ATE196977T1/de active
- 1995-07-20 SK SK86-97A patent/SK283014B6/sk not_active IP Right Cessation
- 1995-07-20 EG EG61395A patent/EG20395A/xx active
- 1995-07-20 UA UA97020754A patent/UA51628C2/uk unknown
- 1995-07-20 RU RU97102821/04A patent/RU2153257C2/ru not_active IP Right Cessation
- 1995-07-20 ES ES95926401T patent/ES2153041T3/es not_active Expired - Lifetime
- 1995-07-20 IL IL11468795A patent/IL114687A/xx not_active IP Right Cessation
- 1995-07-20 HU HU9700195A patent/HU214978B/hu not_active IP Right Cessation
- 1995-07-20 AU AU30805/95A patent/AU700287B2/en not_active Ceased
- 1995-07-20 PL PL95318328A patent/PL187164B1/pl unknown
- 1995-07-20 MX MX9700494A patent/MX9700494A/es 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 CA CA002192989A patent/CA2192989C/fr not_active Expired - Fee Related
- 1995-07-20 PT PT95926401T patent/PT773720E/pt unknown
- 1995-07-20 NZ NZ290153A patent/NZ290153A/xx not_active IP Right Cessation
- 1995-07-20 US US08/776,064 patent/US5906986A/en not_active Expired - Lifetime
- 1995-07-20 CN CN95194227A patent/CN1092484C/zh not_active Expired - Lifetime
- 1995-07-20 DE DE69519170T patent/DE69519170T2/de not_active Expired - Lifetime
- 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
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR100392825B1 (ko) | 2-์ด๋ฏธ๋ค์กธ๋ฆฐ-5-์จ์ ํจ์ ํ๋ ์ด์ง๊ท ์ฑ ์กฐ์ฑ๋ฌผ ๋ฐ ์ด๋ฅผ ์ด์ฉํ ๋์๋ฌผ ๋ณ์์ฑ ์ง๊ท ๋ฅ์ ํด์น๋ฐฉ๋ฒ | |
| TW590741B (en) | Fungicidal active compound combinations | |
| JP3911020B2 (ja) | ในใใญใใซใชใณ้กไผผๅๅ็ฉใๅซใ็ธไนไฝ็จๆงๆฎบ่ๅค็ตๆ็ฉ | |
| JP2015500870A (ja) | ในใใญใใซใชใณ้ ๅ็ฉ | |
| JP4104165B2 (ja) | ในใใญใใซใชใณใซ้กไผผใใๅๅ็ฉใๅซๆใใ็ธไนไฝ็จๆงๆฎบ่ๅค็ตๆ็ฉ | |
| TW529907B (en) | Fungicidal compositions containing N-acetonylbenzamides | |
| JP3848530B2 (ja) | ่พฒๅ่ธ็จๆฎบ่็ตๆ็ฉ | |
| TW314451B (enExample) | ||
| JP3869063B2 (ja) | ่พฒๅ่ธ็จๆฎบ่็ตๆ็ฉ | |
| CN108419798A (zh) | ไธ็งๅซ็ฏ่่่บ็ๆ่็ปๅ็ฉๅๅ ถๅบ็จ | |
| CN106922721A (zh) | ไธ็งๆ่็ปๅ็ฉ | |
| CN106922693A (zh) | ไธ็งๆ่็ปๅ็ฉ | |
| CN106922720A (zh) | ไธ็งๆ่็ปๅ็ฉ | |
| CN103392739A (zh) | ไธ็งๅซๆๅ็้ ฐ่่บๅ็กซ้ ธ้้็ๆ่็ปๅ็ฉ | |
| JP2008308432A (ja) | ๆค็ฉ็้ท่ชฟ็ฏๅค | |
| JPS61118303A (ja) | ๅทฅๆฅญ็จๆฎบ่ๅค | |
| JP4385692B2 (ja) | ่พฒๅ่ธ็จๆฎบ่ๅค็ตๆ็ฉ | |
| JPS625904A (ja) | ๆฎบ่็ตๆ็ฉ | |
| CN106508912B (zh) | ๅซๅ็้ ฐ่่บๅ่ ่ๅ็็ปๅ็ฉๅๅ ถๅถๅๅๅบ็จ | |
| WO2025068980A1 (en) | A synergistic composition comprising a triazolinthione fungicide and process of preparation thereof | |
| CN100352348C (zh) | ็ฏ่่้ ฏไธ้่ฒๆฐฐ็ๆ่็ปๅ็ฉ | |
| JP2820680B2 (ja) | ่พฒๅ่ธ็จๆฎบ่็ตๆ็ฉ | |
| CN116076510A (zh) | ๅคๅไปฃ3-่ฏๅนถๅๅ้ ฎ่บ็ฏๅทฑ็ฏ่ก็็ฉไฝไธบๆ่ๅๅจ้ฒๆฒปๆค็ฉ็ ่ไธญ็ๅบ็จ | |
| JPH06227915A (ja) | ใขใพใผใซๅๅ็ฉใๅซๆใใ่พฒๅ่ธ็จๆฎบ่็ตๆ็ฉ | |
| JPH04154704A (ja) | ่พฒๅ่ธ็จๆฎบ่ๅค็ตๆ็ฉ |