KR20220075235A - 농약 혼합물 - Google Patents
농약 혼합물 Download PDFInfo
- Publication number
- KR20220075235A KR20220075235A KR1020227014631A KR20227014631A KR20220075235A KR 20220075235 A KR20220075235 A KR 20220075235A KR 1020227014631 A KR1020227014631 A KR 1020227014631A KR 20227014631 A KR20227014631 A KR 20227014631A KR 20220075235 A KR20220075235 A KR 20220075235A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- independently
- substituents
- halogen
- occurrence
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
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- 239000000203 mixture Substances 0.000 title claims description 293
- 239000000575 pesticide Substances 0.000 title claims description 68
- PXBFMLJZNCDSMP-UHFFFAOYSA-N 2-Aminobenzamide Chemical class NC(=O)C1=CC=CC=C1N PXBFMLJZNCDSMP-UHFFFAOYSA-N 0.000 claims abstract description 122
- 239000000417 fungicide Substances 0.000 claims abstract description 105
- 229930182692 Strobilurin Natural products 0.000 claims abstract description 94
- 239000002917 insecticide Substances 0.000 claims abstract description 88
- 230000000855 fungicidal effect Effects 0.000 claims abstract description 85
- -1 nitro, hydroxyl Chemical group 0.000 claims description 236
- 125000001424 substituent group Chemical group 0.000 claims description 128
- 241000196324 Embryophyta Species 0.000 claims description 98
- 229910052736 halogen Inorganic materials 0.000 claims description 96
- 150000002367 halogens Chemical class 0.000 claims description 96
- 229910052739 hydrogen Inorganic materials 0.000 claims description 96
- 239000001257 hydrogen Substances 0.000 claims description 84
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 82
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 72
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 66
- 150000002431 hydrogen Chemical class 0.000 claims description 66
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 62
- 238000000034 method Methods 0.000 claims description 61
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 60
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 60
- PSOVNZZNOMJUBI-UHFFFAOYSA-N chlorantraniliprole Chemical compound CNC(=O)C1=CC(Cl)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl PSOVNZZNOMJUBI-UHFFFAOYSA-N 0.000 claims description 59
- 239000005886 Chlorantraniliprole Substances 0.000 claims description 58
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 50
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 50
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 48
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 42
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 40
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 39
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 36
- 239000005730 Azoxystrobin Substances 0.000 claims description 35
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical group CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 claims description 35
- 150000001875 compounds Chemical class 0.000 claims description 34
- 239000005941 Thiamethoxam Substances 0.000 claims description 33
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 claims description 33
- 230000002195 synergetic effect Effects 0.000 claims description 32
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims description 30
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 30
- 241000238631 Hexapoda Species 0.000 claims description 27
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 26
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- 229910052799 carbon Inorganic materials 0.000 claims description 24
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 24
- 229910052717 sulfur Inorganic materials 0.000 claims description 24
- 241000244206 Nematoda Species 0.000 claims description 22
- 239000000463 material Substances 0.000 claims description 20
- 230000001276 controlling effect Effects 0.000 claims description 19
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 18
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 18
- 125000001072 heteroaryl group Chemical group 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 18
- 229910052760 oxygen Inorganic materials 0.000 claims description 18
- 208000031888 Mycoses Diseases 0.000 claims description 14
- 239000003905 agrochemical Substances 0.000 claims description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- 238000005507 spraying Methods 0.000 claims description 13
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 12
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
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- 240000000111 Saccharum officinarum Species 0.000 claims description 11
- 239000004094 surface-active agent Substances 0.000 claims description 11
- 235000007201 Saccharum officinarum Nutrition 0.000 claims description 10
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 10
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- 239000012872 agrochemical composition Substances 0.000 claims description 7
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- 125000004641 (C1-C12) haloalkyl group Chemical group 0.000 claims description 6
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 6
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims description 6
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
- 150000001204 N-oxides Chemical class 0.000 claims description 6
- VQEKJSSQZKIVQF-UHFFFAOYSA-N NS=O Chemical compound NS=O VQEKJSSQZKIVQF-UHFFFAOYSA-N 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims description 6
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
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- 239000005857 Trifloxystrobin Substances 0.000 claims description 5
- WXUZAHCNPWONDH-DYTRJAOYSA-N dimoxystrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1COC1=CC(C)=CC=C1C WXUZAHCNPWONDH-DYTRJAOYSA-N 0.000 claims description 5
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- 230000001105 regulatory effect Effects 0.000 claims description 5
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 claims description 5
- WCXDHFDTOYPNIE-RIYZIHGNSA-N (E)-acetamiprid Chemical group N#C/N=C(\C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-RIYZIHGNSA-N 0.000 claims description 4
- RAMUASXTSSXCMB-UHFFFAOYSA-N 3-bromo-N-{2-bromo-4-chloro-6-[(1-cyclopropylethyl)carbamoyl]phenyl}-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide Chemical compound C1CC1C(C)NC(=O)C1=CC(Cl)=CC(Br)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl RAMUASXTSSXCMB-UHFFFAOYSA-N 0.000 claims description 4
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- DVBUIBGJRQBEDP-UHFFFAOYSA-N cyantraniliprole Chemical compound CNC(=O)C1=CC(C#N)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl DVBUIBGJRQBEDP-UHFFFAOYSA-N 0.000 claims description 4
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- JHIPUJPTQJYEQK-ZLHHXESBSA-N orysastrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1CO\N=C(/C)\C(=N\OC)\C(\C)=N\OC JHIPUJPTQJYEQK-ZLHHXESBSA-N 0.000 claims description 4
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- PDPWCKVFIFAQIQ-UHFFFAOYSA-N 2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide Chemical compound CNC(=O)C(OC)C1=CC=CC=C1COC1=CC(C)=CC=C1C PDPWCKVFIFAQIQ-UHFFFAOYSA-N 0.000 claims description 3
- ONILAONOGQYBHW-UHFFFAOYSA-N 5-bromo-n-[2,4-dichloro-6-(methylcarbamoyl)phenyl]-2-(3,5-dichloropyridin-2-yl)pyrazole-3-carboxamide Chemical compound CNC(=O)C1=CC(Cl)=CC(Cl)=C1NC(=O)C1=CC(Br)=NN1C1=NC=C(Cl)C=C1Cl ONILAONOGQYBHW-UHFFFAOYSA-N 0.000 claims description 3
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- ZMRUPTIKESYGQW-UHFFFAOYSA-N propranolol hydrochloride Chemical compound [H+].[Cl-].C1=CC=C2C(OCC(O)CNC(C)C)=CC=CC2=C1 ZMRUPTIKESYGQW-UHFFFAOYSA-N 0.000 description 1
- 235000015136 pumpkin Nutrition 0.000 description 1
- 235000021013 raspberries Nutrition 0.000 description 1
- 235000012950 rattan cane Nutrition 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 230000026267 regulation of growth Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000035806 respiratory chain Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 102000042094 ryanodine receptor (TC 1.A.3.1) family Human genes 0.000 description 1
- 108091052345 ryanodine receptor (TC 1.A.3.1) family Proteins 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 230000005582 sexual transmission Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000005082 stem growth Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- 239000004548 suspo-emulsion Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 241000228158 x Triticosecale Species 0.000 description 1
- 239000010457 zeolite 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
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- 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
- A01N43/713—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- 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
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P21/00—Plant growth regulators
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P3/00—Fungicides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P5/00—Nematocides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P7/00—Arthropodicides
- A01P7/04—Insecticides
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Insects & Arthropods (AREA)
- Botany (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compounds Of Unknown Constitution (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201962909826P | 2019-10-03 | 2019-10-03 | |
| US62/909,826 | 2019-10-03 | ||
| PCT/IL2020/051070 WO2021064731A1 (en) | 2019-10-03 | 2020-10-01 | Pesticidal mixtures |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20220075235A true KR20220075235A (ko) | 2022-06-07 |
Family
ID=72944223
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020227014631A Withdrawn KR20220075235A (ko) | 2019-10-03 | 2020-10-01 | 농약 혼합물 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US20220400677A1 (https=) |
| JP (1) | JP2022550849A (https=) |
| KR (1) | KR20220075235A (https=) |
| CN (1) | CN114745957A (https=) |
| AR (1) | AR120135A1 (https=) |
| AU (1) | AU2020359089A1 (https=) |
| BR (1) | BR112022006460A2 (https=) |
| CO (1) | CO2022003695A2 (https=) |
| IL (1) | IL291865A (https=) |
| MX (1) | MX2022003931A (https=) |
| PE (1) | PE20221763A1 (https=) |
| PH (1) | PH12022550789A1 (https=) |
| WO (1) | WO2021064731A1 (https=) |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10319591A1 (de) * | 2003-05-02 | 2004-11-18 | Bayer Cropscience Ag | Wirkstoffkombinationen mit nematiziden, insektiziden und fungiziden Eigenschaften basierend auf Trifluorbutenyl-Verbindungen |
| CA2556300C (en) * | 2004-02-24 | 2013-03-19 | Sumitomo Chemical Takeda Agro Company, Limited | Insecticide compositions |
| JP5449669B2 (ja) * | 2006-12-14 | 2014-03-19 | 石原産業株式会社 | 有害生物防除組成物 |
| JP6069193B2 (ja) * | 2010-06-18 | 2017-02-01 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | 殺虫特性及び殺ダニ特性を有する活性物質組合せ |
| UA111593C2 (uk) * | 2010-07-07 | 2016-05-25 | Баєр Інтеллекчуел Проперті Гмбх | Аміди антранілової кислоти у комбінації з фунгіцидами |
| CN102318610B (zh) * | 2011-07-25 | 2013-08-28 | 吴元林 | 一种含有氯虫苯甲酰胺的种子处理剂组合物及其应用 |
| JP6712819B2 (ja) * | 2013-11-14 | 2020-06-24 | 大谷 勝 | バナナ由来組成物を含有する生理活性物質 |
| CN104222156B (zh) * | 2014-09-05 | 2017-11-21 | 杨新兰 | 一种含康宽和腐殖酸的甘蔗杀虫颗粒剂 |
| CN104430477A (zh) * | 2014-11-25 | 2015-03-25 | 广东中迅农科股份有限公司 | 一种含有氟噻虫砜和烟碱类杀虫剂的农药组合物 |
| CN104430478A (zh) * | 2014-11-25 | 2015-03-25 | 广东中迅农科股份有限公司 | 一种水稻杀虫杀菌组合物 |
| CN104542683A (zh) * | 2014-12-31 | 2015-04-29 | 海利尔药业集团股份有限公司 | 一种含有氟噻虫砜与噻虫嗪的杀线虫组合物 |
| CN104798805A (zh) * | 2015-03-26 | 2015-07-29 | 河北博嘉农业有限公司 | 一种用于玉米的杀虫组合物 |
| CN105941460A (zh) * | 2016-06-21 | 2016-09-21 | 南京华洲药业有限公司 | 一种含溴氰虫酰胺和噻虫嗪的增效杀虫组合物及其应用 |
| AU2018279252B2 (en) * | 2017-06-09 | 2024-05-02 | Upl Ltd | Novel pesticidal combinations |
| CN108294007A (zh) * | 2017-12-27 | 2018-07-20 | 青岛奥迪斯生物科技有限公司 | 一种含有氟唑菌苯胺、嘧菌酯的杀菌组合物 |
| CN108402050A (zh) * | 2018-03-23 | 2018-08-17 | 北京科发伟业农药技术中心 | 含氯虫苯甲酰胺的组合物 |
| MX2020013170A (es) * | 2018-06-13 | 2021-02-18 | Adama Makhteshim Ltd | Composicion agricola. |
-
2020
- 2020-10-01 CN CN202080082045.1A patent/CN114745957A/zh active Pending
- 2020-10-01 MX MX2022003931A patent/MX2022003931A/es unknown
- 2020-10-01 BR BR112022006460A patent/BR112022006460A2/pt unknown
- 2020-10-01 KR KR1020227014631A patent/KR20220075235A/ko not_active Withdrawn
- 2020-10-01 WO PCT/IL2020/051070 patent/WO2021064731A1/en not_active Ceased
- 2020-10-01 AR ARP200102730A patent/AR120135A1/es unknown
- 2020-10-01 PH PH1/2022/550789A patent/PH12022550789A1/en unknown
- 2020-10-01 JP JP2022520417A patent/JP2022550849A/ja active Pending
- 2020-10-01 US US17/765,651 patent/US20220400677A1/en not_active Abandoned
- 2020-10-01 AU AU2020359089A patent/AU2020359089A1/en not_active Abandoned
- 2020-10-01 IL IL291865A patent/IL291865A/en unknown
- 2020-10-01 PE PE2022000477A patent/PE20221763A1/es unknown
-
2022
- 2022-03-28 CO CONC2022/0003695A patent/CO2022003695A2/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PH12022550789A1 (en) | 2023-07-31 |
| CO2022003695A2 (es) | 2022-04-19 |
| WO2021064731A1 (en) | 2021-04-08 |
| JP2022550849A (ja) | 2022-12-05 |
| CN114745957A (zh) | 2022-07-12 |
| IL291865A (en) | 2022-06-01 |
| MX2022003931A (es) | 2022-04-25 |
| AR120135A1 (es) | 2022-02-02 |
| PE20221763A1 (es) | 2022-11-11 |
| AU2020359089A1 (en) | 2022-05-19 |
| US20220400677A1 (en) | 2022-12-22 |
| BR112022006460A2 (pt) | 2022-07-19 |
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Legal Events
| Date | Code | Title | Description |
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| PA0105 | International application |
Patent event date: 20220429 Patent event code: PA01051R01D Comment text: International Patent Application |
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Comment text: [Withdrawal of Procedure relating to Patent, etc.] Withdrawal (Abandonment) Patent event code: PC12021R01D Patent event date: 20250407 |
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