EA013316B1 - Масляный суспензионный концентрат с микрокапсулированными агрохимическими биологически активными веществами - Google Patents

Info

Publication number

EA013316B1

EA013316B1 EA200900855A EA200900855A EA013316B1 EA 013316 B1 EA013316 B1 EA 013316B1 EA 200900855 A EA200900855 A EA 200900855A EA 200900855 A EA200900855 A EA 200900855A EA 013316 B1 EA013316 B1 EA 013316B1

Authority

EA

Eurasian Patent Office

Prior art keywords

biologically active

active substances

alkyl

methyl

suspension concentrate

Prior art date

2007-01-23

Links

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• Global Dossier
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• 239000012141 concentrate Substances 0.000 title claims abstract description 44
• 239000012053 oil suspension Substances 0.000 title claims abstract description 43
• 239000003905 agrochemical Substances 0.000 title claims abstract description 37
• 239000004480 active ingredient Substances 0.000 title abstract 3
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 36
• 239000000654 additive Substances 0.000 claims abstract description 9
• -1 dioxazine pyridyl sulfonylurea Chemical class 0.000 claims description 288
• 239000013543 active substance Substances 0.000 claims description 80
• 150000003839 salts Chemical class 0.000 claims description 53
• 239000000126 substance Substances 0.000 claims description 46
• 241000196324 Embryophyta Species 0.000 claims description 45
• 238000002360 preparation method Methods 0.000 claims description 42
• 238000000034 method Methods 0.000 claims description 31
• 239000012071 phase Substances 0.000 claims description 26
• 239000003094 microcapsule Substances 0.000 claims description 23
• 229940100389 Sulfonylurea Drugs 0.000 claims description 18
• 230000007062 hydrolysis Effects 0.000 claims description 16
• 238000006460 hydrolysis reaction Methods 0.000 claims description 16
• 125000003118 aryl group Chemical group 0.000 claims description 15
• 239000008346 aqueous phase Substances 0.000 claims description 8
• 239000000546 pharmaceutical excipient Substances 0.000 claims description 7
• 239000002775 capsule Substances 0.000 claims description 6
• YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims description 5
• 238000002844 melting Methods 0.000 claims description 4
• 230000008018 melting Effects 0.000 claims description 4
• 239000005601 Propoxycarbazone Substances 0.000 claims description 3
• JTHMVYBOQLDDIY-UHFFFAOYSA-N methyl 2-[(4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carbonyl)sulfamoyl]benzoate Chemical compound O=C1N(C)C(OCCC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1C(=O)OC JTHMVYBOQLDDIY-UHFFFAOYSA-N 0.000 claims description 3
• FIBLLDXAIFHZIW-UHFFFAOYSA-N n-(benzenesulfonyl)-5-oxo-4h-triazole-1-carboxamide Chemical compound N1=NCC(=O)N1C(=O)NS(=O)(=O)C1=CC=CC=C1 FIBLLDXAIFHZIW-UHFFFAOYSA-N 0.000 claims description 3
• 230000035945 sensitivity Effects 0.000 claims description 3
• 239000002689 soil Substances 0.000 claims description 3
• GHDLZGOOOLEJKI-UHFFFAOYSA-N benzenesulfonylurea Chemical compound NC(=O)NS(=O)(=O)C1=CC=CC=C1 GHDLZGOOOLEJKI-UHFFFAOYSA-N 0.000 claims 2
• PRZRAMLXTKZUHF-UHFFFAOYSA-N 5-oxo-n-sulfonyl-4h-triazole-1-carboxamide Chemical compound O=S(=O)=NC(=O)N1N=NCC1=O PRZRAMLXTKZUHF-UHFFFAOYSA-N 0.000 claims 1
• 238000002144 chemical decomposition reaction Methods 0.000 claims 1
• 239000002671 adjuvant Substances 0.000 abstract description 2
• 150000003254 radicals Chemical class 0.000 description 69
• 229910052739 hydrogen Inorganic materials 0.000 description 68
• 125000004432 carbon atom Chemical group C* 0.000 description 67
• 150000001875 compounds Chemical class 0.000 description 65
• 239000001257 hydrogen Substances 0.000 description 64
• 229910052736 halogen Inorganic materials 0.000 description 59
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 58
• 150000002367 halogens Chemical class 0.000 description 53
• OAWUUPVZMNKZRY-UHFFFAOYSA-N cyprosulfamide Chemical compound COC1=CC=CC=C1C(=O)NS(=O)(=O)C1=CC=C(C(=O)NC2CC2)C=C1 OAWUUPVZMNKZRY-UHFFFAOYSA-N 0.000 description 48
• 239000003921 oil Substances 0.000 description 46
• 235000019198 oils Nutrition 0.000 description 46
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 44
• 125000000217 alkyl group Chemical group 0.000 description 36
• 239000004009 herbicide Substances 0.000 description 36
• 239000002253 acid Substances 0.000 description 35
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 34
• 239000003112 inhibitor Substances 0.000 description 33
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 32
• 150000002431 hydrogen Chemical class 0.000 description 30
• 125000004093 cyano group Chemical group *C#N 0.000 description 29
• 239000000460 chlorine Substances 0.000 description 28
• 229910052801 chlorine Inorganic materials 0.000 description 27
• 125000003342 alkenyl group Chemical group 0.000 description 26
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 25
• 229940088623 biologically active substance Drugs 0.000 description 25
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 24
• 125000003545 alkoxy group Chemical group 0.000 description 24
• 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 22
• 239000004215 Carbon black (E152) Substances 0.000 description 22
• 125000000304 alkynyl group Chemical group 0.000 description 22
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 22
• 229930195733 hydrocarbon Natural products 0.000 description 22
• 230000001681 protective effect Effects 0.000 description 22
• 239000011737 fluorine Substances 0.000 description 21
• 229910052731 fluorine Inorganic materials 0.000 description 21
• 125000000623 heterocyclic group Chemical group 0.000 description 19
• 125000004414 alkyl thio group Chemical group 0.000 description 18
• 150000007513 acids Chemical class 0.000 description 17
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 17
• 125000003282 alkyl amino group Chemical group 0.000 description 15
• 230000002363 herbicidal effect Effects 0.000 description 15
• 125000005842 heteroatom Chemical group 0.000 description 15
• 239000000203 mixture Substances 0.000 description 15
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 15
• 125000001424 substituent group Chemical group 0.000 description 14
• XFNJVKMNNVCYEK-UHFFFAOYSA-N 1-naphthaleneacetamide Chemical compound C1=CC=C2C(CC(=O)N)=CC=CC2=C1 XFNJVKMNNVCYEK-UHFFFAOYSA-N 0.000 description 13
• 125000002947 alkylene group Chemical group 0.000 description 13
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 13
• 229910052794 bromium Inorganic materials 0.000 description 13
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
• OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical group CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 description 12
• XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 12
• 125000001188 haloalkyl group Chemical group 0.000 description 12
• 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 11
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 11
• YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 11
• 239000005562 Glyphosate Substances 0.000 description 11
• 125000004448 alkyl carbonyl group Chemical group 0.000 description 11
• 125000000753 cycloalkyl group Chemical group 0.000 description 11
• 150000002148 esters Chemical class 0.000 description 11
• 229940097068 glyphosate Drugs 0.000 description 11
• XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 11
• 229910052760 oxygen Inorganic materials 0.000 description 11
• 229920006395 saturated elastomer Polymers 0.000 description 11
• 125000004453 alkoxycarbonyl group Chemical group 0.000 description 10
• 125000004390 alkyl sulfonyl group Chemical group 0.000 description 10
• BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical compound C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 description 10
• IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 9
• 125000004429 atom Chemical group 0.000 description 9
• 230000015572 biosynthetic process Effects 0.000 description 9
• 125000004663 dialkyl amino group Chemical group 0.000 description 9
• 125000001153 fluoro group Chemical group F* 0.000 description 9
• 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 9
• 125000005843 halogen group Chemical group 0.000 description 9
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 9
• BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 description 9
• 239000005561 Glufosinate Substances 0.000 description 8
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 8
• 125000004644 alkyl sulfinyl group Chemical group 0.000 description 8
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 8
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 8
• 239000007788 liquid Substances 0.000 description 8
• 239000003960 organic solvent Substances 0.000 description 8
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 8
• 239000000047 product Substances 0.000 description 8
• 229910052708 sodium Inorganic materials 0.000 description 8
• 239000011734 sodium Substances 0.000 description 8
• 241000894007 species Species 0.000 description 8
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 7
• 125000003277 amino group Chemical group 0.000 description 7
• 150000001768 cations Chemical class 0.000 description 7
• 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 7
• 239000000839 emulsion Substances 0.000 description 7
• 125000004438 haloalkoxy group Chemical group 0.000 description 7
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
• 229910052757 nitrogen Inorganic materials 0.000 description 7
• 229910052700 potassium Inorganic materials 0.000 description 7
• 239000004094 surface-active agent Substances 0.000 description 7
• 230000009261 transgenic effect Effects 0.000 description 7
• 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 description 6
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 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 description 6
• JUJFQMPKBJPSFZ-UHFFFAOYSA-M Iodosulfuron-methyl-sodium Chemical compound [Na+].COC(=O)C1=CC=C(I)C=C1S(=O)(=O)[N-]C(=O)NC1=NC(C)=NC(OC)=N1 JUJFQMPKBJPSFZ-UHFFFAOYSA-M 0.000 description 6
• YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 6
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
• 125000002252 acyl group Chemical group 0.000 description 6
• 229910052784 alkaline earth metal Inorganic materials 0.000 description 6
• 125000005907 alkyl ester group Chemical group 0.000 description 6
• 150000001412 amines Chemical class 0.000 description 6
• 125000003710 aryl alkyl group Chemical group 0.000 description 6
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
• 125000001309 chloro group Chemical group Cl* 0.000 description 6
• 244000038559 crop plants Species 0.000 description 6
• 235000014113 dietary fatty acids Nutrition 0.000 description 6
• 229930195729 fatty acid Natural products 0.000 description 6
• 239000000194 fatty acid Substances 0.000 description 6
• 239000001301 oxygen Substances 0.000 description 6
• 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 6
• 229920000642 polymer Polymers 0.000 description 6
• 235000019260 propionic acid Nutrition 0.000 description 6
• IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 6
• 125000006413 ring segment Chemical group 0.000 description 6
• 159000000000 sodium salts Chemical class 0.000 description 6
• 239000002904 solvent Substances 0.000 description 6
• 229910052717 sulfur Inorganic materials 0.000 description 6
• 239000011593 sulfur Substances 0.000 description 6
• DQKWXTIYGWPGOO-UHFFFAOYSA-N (2,6-dibromo-4-cyanophenyl) octanoate Chemical compound CCCCCCCC(=O)OC1=C(Br)C=C(C#N)C=C1Br DQKWXTIYGWPGOO-UHFFFAOYSA-N 0.000 description 5
• 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 5
• PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 description 5
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
• LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 5
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
• 239000005560 Foramsulfuron Substances 0.000 description 5
• 239000005574 MCPA Substances 0.000 description 5
• DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 5
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 5
• WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 5
• 125000003302 alkenyloxy group Chemical group 0.000 description 5
• 150000001408 amides Chemical class 0.000 description 5
• 150000003863 ammonium salts Chemical class 0.000 description 5
• MKQSWTQPLLCSOB-UHFFFAOYSA-N benzyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate Chemical compound N1=C(Cl)SC(C(=O)OCC=2C=CC=CC=2)=C1C(F)(F)F MKQSWTQPLLCSOB-UHFFFAOYSA-N 0.000 description 5
• 150000004657 carbamic acid derivatives Chemical class 0.000 description 5
• 235000013877 carbamide Nutrition 0.000 description 5
• 229910052799 carbon Inorganic materials 0.000 description 5
• ICJSJAJWTWPSBD-UHFFFAOYSA-N cloquintocet Chemical compound C1=CN=C2C(OCC(=O)O)=CC=C(Cl)C2=C1 ICJSJAJWTWPSBD-UHFFFAOYSA-N 0.000 description 5
• 239000013256 coordination polymer Substances 0.000 description 5
• IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 5
• 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 5
• 150000004665 fatty acids Chemical class 0.000 description 5
• PXDNXJSDGQBLKS-UHFFFAOYSA-N foramsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(NC=O)C=2)C(=O)N(C)C)=N1 PXDNXJSDGQBLKS-UHFFFAOYSA-N 0.000 description 5
• 239000000417 fungicide Substances 0.000 description 5
• 230000001939 inductive effect Effects 0.000 description 5
• 239000002917 insecticide Substances 0.000 description 5
• MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical compound C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 description 5
• 150000007524 organic acids Chemical class 0.000 description 5
• 239000012074 organic phase Substances 0.000 description 5
• XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 5
• 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 description 4
• 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 4
• RBSXHDIPCIWOMG-UHFFFAOYSA-N 1-(4,6-dimethoxypyrimidin-2-yl)-3-(2-ethylsulfonylimidazo[1,2-a]pyridin-3-yl)sulfonylurea Chemical compound CCS(=O)(=O)C=1N=C2C=CC=CN2C=1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 RBSXHDIPCIWOMG-UHFFFAOYSA-N 0.000 description 4
• CLQMBPJKHLGMQK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)nicotinic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C(O)=O CLQMBPJKHLGMQK-UHFFFAOYSA-N 0.000 description 4
• UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 4
• CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 4
• 108010000700 Acetolactate synthase Proteins 0.000 description 4
• 244000291564 Allium cepa Species 0.000 description 4
• 235000002732 Allium cepa var. cepa Nutrition 0.000 description 4
• CTTHWASMBLQOFR-UHFFFAOYSA-N Amidosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)=N1 CTTHWASMBLQOFR-UHFFFAOYSA-N 0.000 description 4
• 239000003666 Amidosulfuron Substances 0.000 description 4
• QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
• 239000005469 Azimsulfuron Substances 0.000 description 4
• 239000005489 Bromoxynil Substances 0.000 description 4
• 239000005504 Dicamba Substances 0.000 description 4
• UWVKRNOCDUPIDM-UHFFFAOYSA-N Ethoxysulfuron Chemical compound CCOC1=CC=CC=C1OS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 UWVKRNOCDUPIDM-UHFFFAOYSA-N 0.000 description 4
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
• 240000004713 Pisum sativum Species 0.000 description 4
• 235000010582 Pisum sativum Nutrition 0.000 description 4
• OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
• 239000005619 Sulfosulfuron Substances 0.000 description 4
• 150000001298 alcohols Chemical class 0.000 description 4
• 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 4
• 229910052783 alkali metal Inorganic materials 0.000 description 4
• 125000004457 alkyl amino carbonyl group Chemical group 0.000 description 4
• 125000005133 alkynyloxy group Chemical group 0.000 description 4
• 150000004945 aromatic hydrocarbons Chemical class 0.000 description 4
• MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 4
• MAHPNPYYQAIOJN-UHFFFAOYSA-N azimsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=CC=2C2=NN(C)N=N2)C)=N1 MAHPNPYYQAIOJN-UHFFFAOYSA-N 0.000 description 4
• 239000004202 carbamide Substances 0.000 description 4
• 150000001735 carboxylic acids Chemical class 0.000 description 4
• VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 description 4
• 125000000392 cycloalkenyl group Chemical group 0.000 description 4
• 125000001316 cycloalkyl alkyl group Chemical group 0.000 description 4
• ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
• 239000003337 fertilizer Substances 0.000 description 4
• 125000000262 haloalkenyl group Chemical group 0.000 description 4
• 125000001072 heteroaryl group Chemical group 0.000 description 4
• SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 description 4
• 229910052740 iodine Inorganic materials 0.000 description 4
• 229910052751 metal Inorganic materials 0.000 description 4
• 239000002184 metal Substances 0.000 description 4
• 238000002156 mixing Methods 0.000 description 4
• 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
• 125000004430 oxygen atom Chemical group O* 0.000 description 4
• 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 4
• 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 4
• 229910052698 phosphorus Inorganic materials 0.000 description 4
• 239000005648 plant growth regulator Substances 0.000 description 4
• 230000027756 respiratory electron transport chain Effects 0.000 description 4
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