BR112021009734B1 - Composição herbicida, seu uso, agente herbicida, e método para controlar plantas daninhas ou para regular o desenvolvimento de plantas - Google Patents
Composição herbicida, seu uso, agente herbicida, e método para controlar plantas daninhas ou para regular o desenvolvimento de plantas Download PDFInfo
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- BR112021009734B1 BR112021009734B1 BR112021009734-1A BR112021009734A BR112021009734B1 BR 112021009734 B1 BR112021009734 B1 BR 112021009734B1 BR 112021009734 A BR112021009734 A BR 112021009734A BR 112021009734 B1 BR112021009734 B1 BR 112021009734B1
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- 241000196324 Embryophyta Species 0.000 title claims abstract description 115
- 239000000203 mixture Substances 0.000 title claims abstract description 114
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 92
- 239000004009 herbicide Substances 0.000 title claims abstract description 80
- 238000000034 method Methods 0.000 title claims abstract description 37
- 230000001105 regulatory effect Effects 0.000 title claims abstract description 4
- 238000011161 development Methods 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 235
- 150000003839 salts Chemical class 0.000 claims abstract description 27
- 244000038559 crop plants Species 0.000 claims description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 239000005562 Glyphosate Substances 0.000 claims description 13
- WYEHFWKAOXOVJD-UHFFFAOYSA-N diflufenican Chemical compound FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 WYEHFWKAOXOVJD-UHFFFAOYSA-N 0.000 claims description 8
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 8
- 238000009331 sowing Methods 0.000 claims description 8
- 238000011282 treatment Methods 0.000 claims description 8
- 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 claims description 7
- 239000005507 Diflufenican Substances 0.000 claims description 7
- 239000000654 additive Substances 0.000 claims description 7
- 229940097068 glyphosate Drugs 0.000 claims description 7
- 239000005561 Glufosinate Substances 0.000 claims description 5
- 230000001276 controlling effect Effects 0.000 claims description 5
- 230000001681 protective effect Effects 0.000 claims description 2
- 230000008121 plant development Effects 0.000 claims 1
- 230000008635 plant growth Effects 0.000 claims 1
- 230000012010 growth Effects 0.000 abstract description 11
- -1 saturated hydrocarbyl radicals Chemical class 0.000 description 147
- 239000001257 hydrogen Substances 0.000 description 38
- 229910052739 hydrogen Inorganic materials 0.000 description 38
- 150000003254 radicals Chemical class 0.000 description 38
- 238000009472 formulation Methods 0.000 description 29
- 229910052736 halogen Inorganic materials 0.000 description 27
- 150000002367 halogens Chemical class 0.000 description 27
- 125000004093 cyano group Chemical group *C#N 0.000 description 26
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 24
- 230000000694 effects Effects 0.000 description 23
- 150000002431 hydrogen Chemical class 0.000 description 21
- 239000000126 substance Substances 0.000 description 20
- 239000003112 inhibitor Substances 0.000 description 19
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 18
- 125000001424 substituent group Chemical group 0.000 description 17
- 239000008187 granular material Substances 0.000 description 14
- 230000009261 transgenic effect Effects 0.000 description 14
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 13
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 13
- 125000004432 carbon atom Chemical group C* 0.000 description 13
- 229910052731 fluorine Inorganic materials 0.000 description 13
- 239000011737 fluorine Substances 0.000 description 13
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- 239000000460 chlorine Substances 0.000 description 12
- 229910052801 chlorine Inorganic materials 0.000 description 12
- 239000011734 sodium Substances 0.000 description 12
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- 125000006536 (C1-C2)alkoxy group Chemical group 0.000 description 11
- 230000009471 action Effects 0.000 description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 11
- 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 10
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- 125000003118 aryl group Chemical group 0.000 description 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 8
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- RUCAXVJJQQJZGU-UHFFFAOYSA-M hydron;2-(phosphonatomethylamino)acetate;trimethylsulfanium Chemical compound C[S+](C)C.OP(O)(=O)CNCC([O-])=O RUCAXVJJQQJZGU-UHFFFAOYSA-M 0.000 description 7
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- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical compound CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 1
- 229960003231 thioacetazone Drugs 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- OPASCBHCTNRLRM-UHFFFAOYSA-N thiometon Chemical compound CCSCCSP(=S)(OC)OC OPASCBHCTNRLRM-UHFFFAOYSA-N 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229950007146 tigolaner Drugs 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- WPALTCMYPARVNV-UHFFFAOYSA-N tolfenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(OC=3C=CC(C)=CC=3)=CC=2)=C1Cl WPALTCMYPARVNV-UHFFFAOYSA-N 0.000 description 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- DDVNRFNDOPPVQJ-HQJQHLMTSA-N transfluthrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=CC(F)=C1F DDVNRFNDOPPVQJ-HQJQHLMTSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- VLCQZHSMCYCDJL-UHFFFAOYSA-N tribenuron methyl Chemical compound COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 VLCQZHSMCYCDJL-UHFFFAOYSA-N 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- 125000004360 trifluorophenyl group Chemical group 0.000 description 1
- ICESBGJHRQHALQ-UHFFFAOYSA-K trisodium;(carboxymethylamino)methyl-hydroxyphosphinate;2-[[hydroxy(oxido)phosphoryl]methylamino]acetate Chemical compound [Na+].[Na+].[Na+].OC(=O)CNCP(O)([O-])=O.OC(=O)CNCP([O-])([O-])=O ICESBGJHRQHALQ-UHFFFAOYSA-K 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 239000012873 virucide Substances 0.000 description 1
- 238000009369 viticulture Methods 0.000 description 1
- 239000000664 voltage gated sodium channel blocking agent Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 229940048462 zinc phosphide Drugs 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
- A01N43/80—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 1,2
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
Abstract
a presente invenção refere-se a composições compreendendo os compostos herbicidamente eficazes (a) e (b), onde (a) representa um ou mais compostos de fórmula geral (i) ou sais agroquimicamente compatíveis dos mesmos [componente (a)], (i) e (b) representa um ou mais herbicidas [componente (b)]. o pedido refere-se ainda a um método e ao uso da composição herbicida de acordo com a invenção para o combate de ervas daninhas ou para regular o crescimento.
Description
[0001] A presente invenção se refere ao campo técnico de produtos para proteção de culturas que podem ser usados para conter o crescimento de plantas indesejadas em terras não cultivadas, para preparação para semeadura ou no cultivo de plantas, e compreendem uma combinação de pelo menos dois herbicidas como compostos herbicidas, onde as composições compreendem os compostos herbicidamente ativos (A) e (B), em que (A) representa um ou mais compostos de Fórmula Geral (I) ou sais agroquimicamente compatíveis dos mesmos [herbicidas (A) ou componentes (A)] e (B) representa um ou mais herbicidas (componente B).
[0002] Compostos da classe estrutural das 3-fenilisoxazolina-5- carboxamidas são conhecidos como herbicidas (vide, por exemplo, o documento WO2012/130798 A). Os compostos são eficazes contra um amplo espectro de plantas daninhas quando aplicados pelo método da pré-emergência ou ainda pelo método da pós-emergência, com a possibilidade de uso não seletivo para controle do crescimento de plantas indesejadas ou uso seletivo em lavouras.
[0003] A eficácia desses herbicidas contra plantas daninhas tem um nível elevado, mas geralmente depende da taxa de aplicação, da forma da respectiva preparação, do espectro de plantas daninhas, das plantas daninhas a serem controladas em cada caso, das condições climáticas e do solo, etc. Um outro critério é a duração da ação ou a taxa de degradação do herbicida. Também a serem levadas em consideração são, onde apropriado, as mudanças na suscetibilidade das plantas daninhas que podem ocorrer com o uso prolongado dos herbicidas ou de forma restrita em termos geográficos. A compensação de perdas da ação no caso de plantas individuais devido ao aumento das taxas de aplicação dos herbicidas só é possível até certo grau, por exemplo, porque tal procedimento frequentemente piora a seletividade dos herbicidas ou porque a ação não é aproveitada, mesmo quando são aplicadas taxas mais altas. Geralmente são necessários métodos para obter uma ação herbicida com uma taxa de aplicação mais baixa dos compostos ativos, uma taxa de aplicação mais baixa não só reduz a quantidade necessária de um composto ativo para aplicação como também geralmente reduz a quantidade necessária de auxiliares de formulação. Ambos reduzem os gastos financeiros e melhora a compatibilidade ambiental do tratamento com herbicidas.
[0004] Uma maneira de aprimorar o perfil de aplicação de um herbicida pode ser combinar o composto ativo com um ou mais outros compostos ativos que contribuem para as propriedades adicionais desejadas. No entanto, na aplicação combinada de uma pluralidade de compostos ativos, com frequência ocorrem fenômenos de incompatibilidade física e biológica, por exemplo, falta de estabilidade em uma coformulação, decomposição de um composto ativo e/ou antagonismo dos compostos ativos. O que se deseja, no entanto, são combinações de compostos ativos tendo um perfil de atividade favorável, alta estabilidade e de forma ideal uma atividade sinergisticamente potencializada inesperada que permite que a taxa de aplicação seja reduzida em relação à aplicação individual dos compostos ativos a serem combinados.
[0005] Um objeto da presente invenção é apresentar composições herbicidas alternativas ou vantajosas que tenham um bom perfil de uso biológico e apresentem tantas das propriedades favoráveis desejáveis mencionadas acima quanto possível.
[0006] Foi agora constatado que, surpreendentemente, este objeto pode ser atingido pelo uso de uma composição compreendendo os compostos herbicidamente ativos (A) e (B), em que (A) representa um ou mais compostos de Fórmula Geral (I) ou sais agroquimicamente compatíveis dos mesmos [componente (A)] e (B) representa um ou mais herbicidas [componente (B)] selecionados do grupo dos compostos herbicidas ativos (B1) to (B11). As composições de acordo com a invenção interagem de maneira particularmente favorável, por exemplo, quando elas são usadas para controlar o crescimento de plantas indesejadas em plantas de lavoura tais como trigo (trigo duro e trigo macio), milho, soja, beterraba, cana-de-açúcar, algodão, arroz, feijões (por exemplo, vagem e feijão-fava), linho, cevada, aveia, centeio, triticale, batata e milhete/sorgo, terras não cultivadas, pastos e gramados/relvados e culturas de plantação.
[0007] A presente invenção apresenta assim composições compreendendo os compostos herbicidamente ativos (A) e (B), onde (A) representa um ou mais compostos de Fórmula Geral (I) ou sais agroquimicamente compatíveis dos mesmos [componente (A)], na qual R1 e R 2 representam, cada um, hidrogênio; R3 representa (C1-C3)-alquila, (C3-C4)-cicloalquila, (C2-C3)- alquenila, (C2-C3)-alquinila ou (C1-C3)-alcóxi, cada um deles substituído com m radicais do grupo que consiste em flúor, cloro, ciano e (C1-C2)-alcóxi; Z representa um grupo Z-1, Z-2, Z-8, Z-9, Z-11 ou Z13, onde Z-1, Z-2, Z-8, Z-9, Z-11 e Z13 têm o seguinte significado: onde a seta em cada caso denota uma ligação ao grupo C=O de Fórmula (I); R11, R12 independentemente um do outro representam hidrogênio, ciano, OR7, S(O)n R5, SO2NR6R7, CO2R8, CONR6R8, COR6, NR6R8, NR6COR8, NR6SO2R8, ou representam (C1-C6)-alquila, (C3-C6)-cicloalquila, (C3-C6)- cicloalquil -(C1-C3)-alquila, (C2-C6)-alquenila, (C5-C6)-cicloalquenila ou (C2-C6)-alquinila, cada um deles opcionalmente substituído com m radicais selecionados do grupo que consiste em halogênio, ciano, OR7, S(O)nR5, CO2R8, NR6SO2R8, ou R11 e R 12 junto com o átomo de nitrogênio ao qual eles estão presos formam um anel saturado, parcialmente ou totalmente insaturado de cinco, seis ou sete membros que é opcionalmente mono- a hexassubstituído com radicais do grupo que consiste em halogênio, ciano, (C1-C6)-alquila, halo-(C1-C6)-alquila, oxo, OR7, S(O)n R5, SO2NR6R7, CO2R8, CONR6R8, e que, além deste átomo de nitrogênio, contém r átomos de carbono, n átomos de oxigênio, p átomos de enxofre e p elementos do grupo que consiste em NR7 e NCOR7 como átomos do anel; X2, X4 e X6 independentemente um do outro representam hidrogênio or flúor; X3 e X5 independentemente um do outro representam hidrogênio, flúor, cloro ou ciano, ou representam (C1-C3)-alquila ou (C1-C3)-alcóxi, cada um deles substituído com m radicais do grupo que consiste em flúor e cloro; R5 representa (C1-C6)-alquila, (C3-C6)-cicloalquila ou arila, cada um deles substituído com m radicais do grupo que consiste em halogênio e ciano; R6 representa hidrogênio or R5; R7 representa hidrogênio, ou representa (C1-C6)-alquila, (C3-C6)-cicloalquila, (C3-C4)- alquenila ou (C3-C4)-alquinila, cada um deles substituído com m radicais do grupo que consiste em halogênio, ciano e (C1-C2)-alcóxi; R8 representa hidrogênio, ou representa (C1-C6)-alquila, (C3-C6)-cicloalquila, (C3-C6)- alquenila ou (C3-C6)-alquinila, cada um deles substituído com m radicais do grupo que consiste em halogênio, ciano e (C1-C2)-alcóxi; m o índice é 0, 1, 2 ou 3; n o índice é 0, 1 ou 2; p o índice é 0 ou 1; e r o índice é 3, 4, 5 ou 6; e (8) representa um ou mais herbicidas [componente (B)] do grupo dos compostos herbicidas ativos (B1) a (B11), onde (81) representa compostos herbicidas ativos do grupo dos compostos do tipo diceto selecionados dentre (B1.1) aloxidim, (CAS 55634-91-8), (CAS 55635-13-7) (B1.2) biciclopirona, (CAS 352010-68-5) (B1.3) butroxidim, (CAS 138164-12-2) (B1.4) cletodim, (CAS 99129-21-2) (B1.5) cicloxidim, (CAS 101205-02-1) (B1.6) fenquinotriona, (CAS 1342891-70-6) (B1.7) mesotriona, (CAS 104206-82-8) (B1.8) pinoxaden, (CAS 243973-20-8) (B1.9) profoxidim, (CAS 139001-49-3) (B1.10) setoxidim, (CAS 74051-80-2) (B1.11) sulcotriona, (CAS 99105-77-8) (B1.12) SYP-9121 (CAS 1976053-87-8) (B1.13) tefuriltriona, (CAS 473278-76-1) (B1.14) tembotriona, (CAS 335104-84-2) (B1.15) tepraloxidim, (CAS 149979-41-9) (B1.16) tralcoxidim, (CAS 87820-88-0) (B1.17) Y13161, (CAS 1639426-14-4) (B1.18) Y13287; (CAS 1639426-42-8) (B2) representa compostos herbicidas ativos do grupo das (sulfon)amidas selecionadas dentre (B2.1) acetoclor, (CAS 34256-82-1) (B2.2) alaclor, (CAS 15972-60-8), (B2.3) amidosulfuron, (CAS 120923-37-7) (B2.4) asulam, (CAS 3337-71-1) (CAS 14089-43-1), (CAS 2302-17-2) (B2.5) azimsulfuron, (CAS 120162-55-2) (B2.6) beflubutamid, (CAS 113614-08-7), (CAS 113614-09-8) (B2.7) bensulfuron, (CAS 83055-99-6), (CAS 83055-99-6) (B2.8) butaclor, (CAS 23184-66-99) (B2.9) carbetamida, (CAS 16118-49-3) (B2.10) clorimuron, (CAS 99283-00-8), (CAS 90982-32-4), (B2.11) clorprofam, (CAS 101-21-3) (B2.12) clorsulfuron, (CAS 64902-72-3) (B2.13) cinosulfuron, (CAS 94593-91-6) (B2.14) cloransulam, (CAS159518-97-5), (CAS 147150-35-4) (B2.15) ciclosulfamuron, (CAS 136849-15-5) (B2.16) desmedifam, (CAS 13684-56-5) (B2.17) diclosulam, (CAS 145701-21-9) (B2.18) diflufenican, (CAS 83164-33-4) (B2.19) dimetaclor, (CAS 50563-36-5) (B2.20) dimetenamida, (CAS 87674-68-8), (CAS 163515-14-8) (B2.21) esprocarb (CAS 85785-20-2) (B2.22) etametsulfuron, (CAS 111353-84-5), (CAS 97780-06-8) (B2.23) etoxisulfuron, (CAS 126801-58-9) (B2.24) flazasulfuron, (CAS 104040-78-0) (B2.25) florasulam, (CAS 145701-23-1) (B2.26) flucarbazona, (CAS 145026-88-6 ), (CAS 181274-17-9) (B2.27) flucetosulfuron, (CAS 412928-75-7) (B2.28) flufenacet, (CAS 142459-58-3) (B2.29) flumetsulam, (CAS 98967-40-9) (B2.30) flupirsulfuron, (CAS 150315-10-9), (CAS 144740-53-4), (CAS 144740-54-5) (B2.31) foramsulfuron, (CAS 173159-57-4) (B2.32) halosulfuron, (CAS 135397-30-7), (CAS 100784-20-1) (B2.33) imazosulfuron, (CAS 122548-33-8) (B2.34) iodosulfuron, (CAS 185119-76-0), (CAS 144550-06-1), (CAS 144550-36-7) (B2.35) ipfencarbazona, (CAS 212201-70-2) (B2.36) mefenacet, (CAS 73250-68-7) (B2.37) mesosulfuron, (CAS 400852-66-6), (CAS 208465-21-8) (B2.38) metazaclor, (CAS 67129-08-2) (B2.39) metazosulfuron, (CAS 868680-84-6) (B2.40) metolaclor, (CAS 51218-45-2) (B2.41) metosulam, (CAS 139528-85-1) (B2.42) metsulfuron, (CAS 79510-48-8), (CAS 74223-64-6) (B2.43) nicosulfuron, (CAS 111991-09-4) (B2.44) ortosulfamuron, (CAS 213464-77-8) (B2.45) oxasulfuron, (CAS 144651-06-9) (B2.46) penoxsulam, (CAS 219714-96-2) (B2.47) petoxamida, (CAS 106700-29-2) (B2.48) fenmedifam, (CAS 13684-63-4) (B2.49) picolinafen, (CAS 137641-05-5) (B2.50) pretilaclor, (CAS 51218-49-6) (B2.51) primisulfuron, (CAS 113036-87-6), (CAS 86209-51-0) (B2.52) propaclor, (CAS 1918-16-7) (B2.53) propanil, (CAS 709-98-8) (B2.54) profam, (CAS 122-42-9) (B2.55) propisoclor, (CAS 86763-47-5) (B2.56) propoxicarbazona, (CAS 145026-81-9), (CAS 181274-15-7) (B2.57) propirisulfuron, (CAS 570415-88-2) (B2.58) propizamida, (CAS 23950-58-5) (B2.59) prosulfocarb, (CAS 52888-80-9) (B2.60) prosulfuron, (CAS 94125-34-5) (B2.61) pirazosulfuron, (CAS 98389-04-9), (CAS 93697-74-6) (B2.62) piroxsulam, (CAS 422556-08-9) (B2.63) rimsulfuron, (CAS 122931-48-0) (B2.64) S-metolaclor, (CAS 87392-12-9) (B2.65) sulfometuron, (CAS 74223-56-6), (CAS 74222-97-2), (CAS 144651- 06-9) (B2.66) sulfosulfuron, (CAS 141776-32-1) (B2.67) tenilclor, (CAS 96491-05-3) (B2.68) tiencarbazona, (CAS 936331-72-5), (CAS 317815-83-1) (B2.69) tifensulfuron, (CAS 79277-67-1), (CAS 79277-27-3) (B2.70) triallate, (CAS 2303-17-5) (B2.71) triasulfuron, (CAS 82097-50-5) (B2.72) tribenuron, (CAS 106040-48-6), (CAS 101200-48-0) (B2.73) trifloxisulfuron, (CAS 145099-21-4, (CAS 199119-58-9) (B2.74) triflusulfuron, (CAS 135990-29-3), (CAS 126535-15-7) (B2.75) tritosulfuron, (CAS 142469-14-5) (B2.76) esprocarb, (CAS 85785-20-2) (B2.77) profluazol, (CAS 190314-43-3) (B2.78) triallate; (CAS 2303-17-5) (B3) representa compostos herbicidas ativos do grupo das arilonitrilas selecionadas dentre (B3.1) bromoxinil, (CAS 1689-84-5) (CAS 3861-41-4), (CAS 56634-95-8), (CAS 1689-99-2), (CAS 2961-68-4) (B3.2) clortiamid, (CAS 1918-13-4) (B3.3) diclobenil, (CAS 1194-65-6) (B3.4) ioxinil, (CAS 1689-83-4), (CAS 2961-61-7), (CAS 3861-47-0), (CAS 2961-62-8) (B3.5) piraclonil; (CAS 158353-15-2) (84) representa compostos herbicidas ativos do grupo dos azóis selecionados dentre (B4.1) amicarbazona, (CAS 129909-90-6) (B4.2) amitrole, (CAS 61-82-5) (B4.3) azafenidin, (CAS 68049-83-2) (B4.4) benzofenap, (CAS 82692-44-2) (B4.5) benzuofucaotong, (CAS 1992017-55-6) (B4.6) biscarfentrazona, (CAS 1622908-18-2) (B4.7) cafenstrole, (CAS 125306-83-4) (B4.8) carfentrazona, (CAS 128621-72-7), (CAS128639-02-1) (B4.9) fentrazamida, (CAS 158237-07-1) (B4.10) imazametabenz, (CAS 100728-84-5), (CAS 81405-85-8) (B4.11) imazamox, (CAS 114311-32-9), (CAS 247057-22-3) (B4.12) imazapic, (CAS 104098-48-8), (CAS 115136-53-3) (B4.13) imazapir, (CAS 81334-34-1), (CAS 81510-83-0) (B4.14) imazaquin, (CAS 81335-37-7), (CAS 81335-47-9), (CAS 81335-43-5), (CAS 81335-46-8) (B4.15) imazetapir, (CAS 81335-77-5), (CAS 101917-66-2) (B4.16) isouron, (CAS 55861-78-4) (B4.17) isoxaben, (CAS 82558-50-7) (B4.18) isoxaflutole, (CAS 141112-29-0) (B4.19) oxadiargil, (CAS 39807-15-3) (B4.20) oxadiazon, (CAS 19666-30-9) (B4.21) piraflufen, (CAS 129630-17-7), (CAS 129630-19-9) (B4.22) pirasulfotole, (CAS 365400-11-9) (B4.23) pirazolinato, (CAS 58011-68-0) (B4.24) pirazoxifen, (CAS 71561-11-0) (B4.25) piroxasulfona, (CAS 447399-55-5) (B4.26) sulfentrazona, (CAS 122836-35-5) (B4.27) tolpiralato, (CAS 1101132-67-5) (B4.28) topramezona, (CAS 210631-68-8) (B4.29) triazolesulcotriona (CAS 1911613-97-2) (QYR-301), (B4.30) QYM-201, (CAS 1855925-45-1) (B4.31) bencarbazona, (CAS 173980-17-1) (B4.32) fluazolato, (CAS 174514-07-9) (B4.33) flupoxam, (CAS 119126-15-7) (B4.34) isoxaclortole; (CAS 141112-06-3) (B5) representa outros compostos herbicidas ativos selecionados dentre (B5.1) aminociclopiraclor, (CAS 858956-08-8), (CAS 858954-83-3), (CAS 858956-35-1) (B5.2) aminopiralid, (CAS 150114-71-9), (CAS 566191-87-5), (CAS 566191-89-7) (B5.3) benazolin-etil, (CAS 3813-05-6), (CAS 38561-76-1), (CAS 25059-80-7), (CAS 67338-65-2) (B5.4) benfluralin, (CAS 1861-40-1) (B5.5) bentazona, (CAS 25057-89-0), (CAS 50723-80-3) (B5.6) benzobiciclon, (CAS 156963-66-5) (B5.7) bixlozona, (CAS 81777-95-9) (B5.8) bromofenoxim, (CAS 13181-17-4) (B5.9) butralin, (CAS 33629-47-9) (B5.10) cloridazon/pirazon, (CAS 1698-60-8) (B5.11) clortal, (CAS 2136-79-0), (CAS 1861-32-1), (CAS 887-54-7) (B5.12) cinidon-etil, (CAS 142891-20-1) (B5.13) cinmetilin, (CAS 87818-31-3) (B5.14) clomazona, (CAS 81777-89-1) (B5.15) ciclopirimorate, (CAS 499231-24-2) (B5.16) dinitramine, (CAS 29091-05-2) (B5.17) diquat, (CAS 2764-72-9), (CAS 85-00-7), (CAS 4032-26-2) (B5.18) ditiopir, (CAS 97886-45-8) (B5.19) ácido acetico, (CAS 64-19-7) (B5.20) etalfluralin, (CAS 55283-68-6) (B5.21) etofumesato, (CAS 26225-79-6) (B5.22) flamprop, (CAS 58667-63-3, (CAS 90134-59-1), (CAS 63782-90-1), (CAS 63729-98-6) (B5.23) florpirauxifen, (CAS 943832-81-3), (CAS 1390661-72-9) (B5.24) flufenpir, (CAS 188490-07-5), (CAS 188489-07-8) (B5.25) flumiclorac, (CAS 87547-04-4), (CAS 87546-18-7) (B5.26) flumioxazin, (CAS 103361-09-7) (B5.27) fluridona, (CAS 59756-60-4) (B5.28) flurocloridona, (CAS 61213-25-0) (B5.29) flurtamona, (CAS 96525-23-4) (B5.30) flutiacet-metil, (CAS 149253-65-6) (B5.31) halauxifen, (CAS 943832-60-8), (CAS 943831-98-9) (B5.32) indanofan, (CAS 13320-30-1) (B5.33) norflurazon, (CAS 27314-13-2) (B5.34) ácido oleico, (CAS 112-80-1) (B5.35) oryzalin, (CAS 19044-88-3) (B5.36) oxaziclomefona, (CAS 153197-14-9) (B5.37) paraquat, (CAS 4685-14-7), (CAS 1910-42-5), (CAS 2074-50-2) (B5.38) ácido pelargonico, (CAS 112-05-0) (B5.39) pendimetalin, (CAS 40487-42-1) (B5.40) pentoxazona, (CAS 110956-75-7) (B5.41) piridafol, (CAS 40020-01-7) (B5.42) piridate, (CAS 55512-33-9) (B5.43) tetflupirolimet, (CAS 2053901-33-8) (B5.44) tiazopir, (CAS 117718-60-2) (B5.45) triafamona, (CAS 874195-61-6) (B5.46) (B5.47) trifluralin, 4-amino-3-cloro-5-fluoro-6- (7-fluoro-1H-indol-6-il) piridine-2-ácido carboxilico, (CAS 1582-09-8) (B5.48) ciclopirimorate, (CAS 499231-24-2) (B5.49) diquat, (CAS 2764-72-9, CAS 85-00-7, CAS4032-26- 2) (B5.50) oxaziclomefona, (CAS 153197-14-9) (B5.51) pentanoclor, (CAS 2307-68-8) (B5.52) tebutam, (CAS 35256-85-0) (B5.53) tidiazimin; (CAS 123249-43-4) (86) representa compostos herbicidas ativos do grupo dos ácidos (het)arilcarboxílicos selecionados dentre (B6.1) cloramben, (CAS 133-90-4), (CAS 1076-46-6), (CAS 53404-16-3), (CAS 7286-84-2), (CAS 25182-03-0), (1954-81-0) (B6.2) clopiralid, (CAS 1702-17-6), (CAS 1532-24-7), (CAS 57754-85-5), (CAS 58509-83-4), (CAS 73455-09-1) (B6.3) dicamba, (CAS 1918-00-9), (CAS 1286239-22-2), (CAS 104040-791), (CAS 2300-66-5), (CAS 25059-78-3), (CAS 55871-028), (CAS 6597-78-0), (CAS 53404-28-7), (CAS 10007-859), (CAS 1982-69-0), (53404-29-8), (CAS 56141-00-5) (B6.4) fluroxipir, (CAS 69377-81-7), (CAS -27-8), (CAS 81406-37-3) (B6.5) picloram, (CAS 1918-02-1), (CAS 55870-98-9), (CAS 36374-99-9), (CAS 26952-20-5), (CAS 14143-55-6), (CAS 55871-00-6), (CAS 2545-60-0), (CAS 35832-11-2), (CAS 6753-47-5), (CAS 82683-78-1) (B6.6) quinclorac, (CAS 84087-01-4), (CAS 84087-48-9), (CAS 84087-33-2) (B6.7) quinmerac, (CAS 90717-03-6) (B6.8) TBA, (CAS 50-31-7), (CAS 3426-62-8), (CAS 71750-37-3), (CAS 4559-30-2), (CAS 2078-42-4) (B6.9) Triclopir; (CAS 55335-06-3), (CAS [64700-56-7), (CAS 1048373 85-8), (CAS 60825-27-6), (CAS 57213-69-1) (87) representa compostos herbicidas ativos do grupo dos compostos de organofósforo selecionados dentre (B7.1) anilofos, (CAS 64249-01-0) (B7.2) bialafos, (CAS 35597-43-4), (CAS 71048-99-2) (B7.3) butamifos, (CAS 36335-67-8) (B7.4) glufosinato, (CAS 51276-47-2), (CAS 35597-44-5), (CAS 77182-82 2), (CAS 70033-13-5) (B7.5) glifosato, (CAS 1071-83-6), (CAS 69254-40-6), (CAS 34494-047), (CAS 38641-94-0), (CAS 40465-66-5), (CAS 3960042-5), (CAS 70393-85-0), (CAS 81591-81-3) (B7.6) piperofos, (CAS 24151-93-7) (B7.7) sulfosato, (CAS 1591-81-3) (B7.8) amiprofos; (CAS 33857-23-7, CAS 36001-88-4) (88) representa compostos herbicidas ativos do grupo dos éteres fenílicos selecionados dentre (B8.1) 2,4-D, (CAS 94-75-7), (CAS 2307-55-3), (CAS 1929-73-3), (CAS 1320-18-9), (CAS 1928-45-6), (CAS 94-80-4), (CAS 1048373-72-3), (CAS 20940-37-8), (CAS 2008-39-1), (CAS 5742-19-8), (CAS 2212-54-6), (CAS 533-23-3), (CAS 1928-43-4), (CAS 37102-63-9), (CAS 713-15-1), (CAS 25168-26-7), (CAS 94-11-1), (CAS 5742-17-6), (CAS 3766-27-6), (CAS 1917-97-1), (CAS 1928-38-7), (CAS 1928-44-5), (CAS 1917-92-6), (CAS 1928-61-6), (CAS 2702-72-9), (CAS 15146-99-3), (CAS 28685-18-9), (CAS 2646-78-8), (CAS 18584-79-7), (CAS 2569-01-9), (CAS 215655-76-8) (B8.2) 2,4-DB, (CAS 94-82-6), (CAS 2758-42-1), (CAS 1320-15-6), (CAS 19480-40-1), (CAS 10433-59-7) (B8.3) 2,4-DP, (CAS 120-36-5), (CAS 53404-31-2), (CAS 53404-32-3), (CAS 79270-78-3), (CAS 28631-35-8), (CAS 57153-17-0), (CAS 5746-17-8), (CAS 39104-30-8) (B8.4) acifluorfen, (CAS 50594-66-6), (CAS 50594-67-7), (CAS 62476-59-9) (B8.5) aclonifen, (CAS 74070-46-5) (B8.6) bifenox, (CAS 42576-02-3) (B8.7) clometoxifen, (CAS 32861-85-1) (B8.8) clodinafop- propargil, (CAS 114420-56-3 ), (CAS 105512-06-9) (B8.9) clomeprop, (CAS 84496-56-0) (B8.10) cihalofop, (CAS 122008-78-0), (CAS 122008-85-9) (B8.11) diclofop, (CAS 40843-25-2 ), (CAS 51338-27-3) (B8.12) etoxifen, (CAS 188634-90-4), (CAS 131086-42-5) (B8.13) fenoxaprop, (CAS 95617-09-7 ), (CAS 113158-40-0), (CAS 71283-80 2) (B8.14) fluazifop, (CAS 69335-91-7), (CAS 83066-88-0), (CAS 79241-46-6) (B8.15) fluoroglicofen, (CAS 77501-60-1), (CAS 77501-90-7) (B8.16) fomesafen, (CAS 72178-02-0), (CAS 108731-70-0) (B8.17) halosafen, (CAS 77227-69-1) (B8.18) haloxifop, (CAS 69806-34-4), (CAS 95977-29-0 ), (CAS 72619-32-0) (B8.19) lactofen, (CAS 77501-63-4) (B8.20) MCPA, (CAS 94-74-6), (CAS 19480-43-4), (CAS 1713-12-8), (CAS 2039-46-5), (CAS 20405-19-0), (CAS 2698-38-6), (CAS 29450-45-1), (CAS 1713-11-7), (CAS 26544-20-7), (CAS 2698-40-0), (CAS 2436-73-9), (CAS 6365-62-4), (CAS 5221-16-9), (CAS 3653-48-3), (CAS 42459-68-7) (B8.21) MCPB, (CAS 94-81-5), (CAS 10443-70-6), (CAS 57153-18-1), (CAS 6062-26-6) (B8.22) mecoprop, (CAS 93-65-2), (CAS 32351-70-5), (CAS 1432-14-0), (CAS 71526-69-7), (CAS 28473-03-2), (CAS 2786-19-8), (CAS 1929-86-8), (CAS 19095-88-6), (CAS 53404-61-8), (CAS 16484-77-8) (B8.23) metamifop, (CAS 256412-89-2) (B8.24) oxifluorfen, (CAS 42874-03-3) (B8.25) propaquizafop, (CAS 111479-05-1) (B8.26) quizalofop, (CAS 76578-12-6), (CAS 76578-14-8), (B8.27) quizalofop-p, (CAS 94051-08-8), (CAS 100646-51-3), (CAS 200509-41-7) (B8.28) benzfendizona; (CAS 158755-95-4) (B9) representa compostos herbicidas ativos do grupo das pirimidinas selecionadas dentre (B9.1) bispirac-sódico, (CAS 125401-92-5) (B9.2) bromacil, (CAS 314-40-9), (CAS 53404-19-6), (CAS 69484-12-4) (B9.3) butafenacil, (CAS 134605-64-4) (B9.4) lenacil, (CAS 2164-08-1) (B9.5) piribenzoxim, (CAS 168088-61-7) (B9.6) piriftalid, (CAS 135186-78-6) (B9.7) piriminobac, (CAS 136191-56-5), (CAS 136191-64-5) (B9.8) pirimisulfan, (CAS 221205-90-9) (B9.9) piritiobac-sódico, (CAS 123342-93-8), (CAS 123343-16-8) (B9.10) saflufenacil, (CAS 372137-35-4) (B9.11) terbacil, (CAS 5902-51-2) (B9.12) tiafenacil, (CAS 1220411-29-9) (B9.13) trifludimoxazin, (CAS 1258836-72-4) (B9.14) etil [3-[2-cloro-4-fluoro-5-(1-metil-6- trifluorometil-2,4-dioxo-1,2,3,4- tetrahidropirimidin-3-il)fenoxi]-2- piridiloxi]acetate; (B10) representa compostos herbicidas ativos do grupo das (tio) ureias selecionadas dentre (B10.1) clorobromuron, (CAS 13360-45-7) (B10.2) clorotoluron, (CAS 15545-48-9) (B10.3) daimuron, (CAS 42609-52-9) (B10.4) dimefuron, (CAS 34205-21-5) (B10.5) diuron, (CAS 330-54-1) (B10.6) diflufenzopir, (CAS 1957168-02-3) (B10.7) fluometuron, (CAS 2164-17-2) (B10.8) isoproturon, (CAS 34123-59-6) (B10.9) linuron, (CAS 330-55-2) (B10.10) metabenztiazuron, (CAS 18691-97-9) (B10.11) metobromuron, (CAS 3060-89-7) (B10.12) metoxuron, (CAS 19937-59-8) (B10.13) monolinuron, (CAS 1746-81-2) (B10.14) neburon, (CAS 555-37-3) (B10.15) siduron, (CAS 1982-49-6) (B10.16) tebutiuron, (CAS 34014-18-1) (B10.17) fenuron, (CAS 101-42-8) (B10.18) cloroxuron, (CAS 1982-47-4) (B10.19) diflufenzopir, (CAS 1957168-02-3, CAS 109293-98-3) (B10.20) etidimuron; (CAS 30043-49-3) (B11) representa compostos herbicidas ativos do grupo das triazinas selecionadas dentre (B11.1) ametrine, (CAS 834-12-8) (B11.2) atrazina, (CAS 1912-24-9) (B11.3) cinazina, (CAS 21725-46-2) (B11.4) dimetametrine, (CAS 22936-75-0) (B11.5) hexazinona, (CAS 51235-04-2) (B11.6) indaziflam, (CAS 950782-86-2) (B11.7) metamitron, (CAS 41394-05-2) (B11.8) metribuzin, (CAS 21087-64-9) (B11.9) prometon, (CAS 1610-18-0) (B11.10) prometrine, (CAS 7287-19-6) (B11.11) propazine, (CAS 139-40-2) (B11.12) simazine, (CAS 122-34-9) (B11.13) simetrine, (CAS 1014-70-6) (B11.14) terbumeton, (CAS 33693-04-8) (B11.15) terbutilazina, (CAS 5915-41-3) (B11.16) terbutrine, (CAS 886-50-0) (B11.17) triaziflam, (CAS 131475-57-5) (B11.18) trietazina, (CAS 1912-26-1) (B11.19) desmetrine (CAS 1014-69-3).
[0008] O nome comum dos herbicidas listados está complementado com o "CAS RN" (número de registro no banco de dados do Chemical Abstracts Service) ("CAS", abreviado) entre parênteses. O CAS RN é um número de referência amplamente utilizado que permite a designação inequívoca das substâncias em questão uma vez que o "CAS RN" faz a distinção, inter alia, entre isômeros, incluindo estereoisômeros, e sais e ésteres. Para compostos ativos que existem em várias formas, o nome do composto neutro está apresentado, em cada caso, na lista acima. Os CAS dados entre parênteses se referem a essas e a todas as outras formas do composto ativo. Apenas o composto neutro é mencionado a seguir, e por isso abrange todas as formas existentes listadas, a menos que uma forma específica do composto ativo seja relevante em um contexto particular, por exemplo, nos quadros de exemplos abaixo indicando a eficácia biológica.
[0009] As composições de acordo com a invenção podem conter ainda componentes, por exemplo, outros compostos ativos para conter organismos nocivos tais como plantas daninhas, animais que danificam as plantas ou fungos que danificam as plantas, especialmente compostos ativos do grupo dos herbicidas, fungicidas, inseticidas, acaricidas, nematicidas e miticidas, e substâncias relacionadas, ou ainda outros tipos de compostos ativos para proteção de lavouras (por exemplo, indutores de resistência), reguladores do crescimento de plantas, e/ou adições e/ou auxiliares de formulação de que são usuais na proteção de lavouras. Os componentes podem ser formulados juntos (formulação pronta para uso) e descritos como tais, ou eles podem ser formulados separadamente e descritos juntos, por exemplo, em uma mistura de tanque ou em aplicação sequencial.
[0010] Os compostos herbicidas ativos individuais de Fórmula Geral (I) presentes como componente (A) também são doravante denominados compostos (A), compostos ativos (A), componente (A) ou herbicidas (A). De forma correspondente, os compostos herbicidas ativos individuais presentes como componente (B) também são doravante denominados compostos (B), compostos ativos (B), componentes (B) ou herbicidas (B).
[0011] Foi constatado que uma propriedade vantajosa da combinação inventiva de herbicidas (A) e (B) é que os compostos ativos (A) e (B) são compatíveis entre si, o que significa que eles podem ser descritos juntos sem a ocorrência de incompatibilidade química significativa entre os compostos ativos (A) e/ou (B) que leve à destruição de um ou mais compostos ativos. Isto evita qualquer redução do teor dos compostos ativos nas formulações líquidos de pulverização. A compatibilidade favorável também se estende às propriedades biológicas dos compostos ativos no uso combinado. Por exemplo, geralmente não são observados efeitos antagonísticos no caso do controle de plantas daninhas com as combinações de compostos ativos de acordo com a invenção. Os compostos ativos (A) e (B) são, assim, particularmente adequados para serem descritos juntos com ou além de outros compostos ativos para proteção de lavouras ou agroquímicos. A aplicação combinada possível permite a utilização de efeitos vantajosos, por exemplo, a ampliação do espectro de plantas daninhas a serem controladas na aplicação, ou a redução da taxa de aplicação dos herbicidas (A) ou (B) individuais em relação à respectiva taxa de aplicação do herbicida em questão no caso de aplicação individual. É assim possível influenciar as características de degradação dos compostos ativos e obter condições mais favoráveis para o subsequente crescimento de plantas de lavoura. Considerada como uma outra vantagem é que o desenvolvimento de resistência das plantas daninhas aos compostos ativos frequentemente pode ser significativamente reduzido ou evitado através da combinação de compostos ativos com diferentes mecanismos de ação.
[0012] Mais particularmente, surpreendentemente ocorrem efeitos superaditivos (= sinergísticos) no caso do uso combinado dos compostos ativos (A) e (B) em um maior número de plantas daninhas economicamente importantes. Aqui, a atividade na combinação é mais alta que a soma esperada das atividades dos herbicidas individuais descritos. Os efeitos sinerfísticos permitem que a taxa de aplicação seja ainda mais reduzida, que um espectro mais amplo de ervas daninhas de folhas largas e gramíneas daninhas seja controlado, um início mais rápido da ação herbicida, persistência mais longa, melhor controle das plantas daninhas com apenas uma ou algumas poucas aplicações e extensão do período de apliacação possível. Até certo ponto, com o uso das composições, a quantidade de ingredientes prejudiciais, tal como nitrogênio ou ácido oleico, e a introdução dos mesmos no solo são igualmente reduzidas.
[0013] As referidas propriedades e vantagens são desejadas no controle prático de ervas daninhas a fim de manter as culturas agrícolas livres de plantas concorrentes indesejadas e assim garantir e/ou aumentar os rendimentos em tgermos de qualidade e quantidade. As novas combinações superam acentuadamente o estado da técnica tendo em vistas as propriedades descritas.
[0014] Os efeitos sinergísticos são observados no caso de distribuição conjunta dos compostos ativos (A) e (B), mas também podem ocorrer com frequência no caso de aplicação separada. Também é possível aplicar os herbicidas (A) ou (B) ou a composição herbicida (A) e (B) em múltiplas porções (aplicação sequencial). Por exemplo, uma ou mais aplicações na pré-emergência podem ser acompanhadas por uma aplicação na pós-emergência, ou uma primeira aplicação na pós-emergência pode ser acompanhada por uma aplicação na pós-emergência razoavelmente posterior ou posterior. Dá-se preferência à aplicacação simultânea ou imediatamente sucessiva dos compostos ativos da respectiva combinação, se apropriado em diversas porções. Porém, a aplicação separada dos compostos ativos individuais de uma combinação também é possível, e pode ser vantajosa no caso individual. Também é possível integrar outros agentes protetores de lavouras no sistema de aplicação, por exemplo, outros compostos ativos mencionados (outros herbicidas, fungicidas, inseticidas, acaricidas etc.) e/ou vários auxiliares, adjuvantes e/ou applicações de fertilizante.
[0015] Por aplicação pelo método da pré-emergência e pelo método da pós-emergência, de acordo com o contexto em que os termos são usados, entende-se respectivamente a aplicação dos compostos ativos antes e depois do aparecimento visível das plantas daninhas acima do solo, ou o uo dos compostos ativos contras as plantas daninhas antes da emergência das plantas de lavoura e depois da emergência das plantas de lavoura.
[0016] Na Fórmula (I) para compostos dos compostos herbicidas ativos (A) e todas as fórmulas que se seguem, aplicam-se as seguintes definições:
[0017] Alquil significa radicais hidrocarbil saturado de cadeia linear ou ramificada tendo o número de átomos de carbono especificado em cada caso, por exemplo, C1-C6-alquil tal como metila, etila, propila, 1- metiletila, butila, 1-metilpropila, 2-metilpropila, 1,1-dimetiletila, pentila, 1-metilbutila, 2-metilbutila, 3-metilbutila, 2,2-dimetilpropila, 1-etilpropila, hexila, 1,1-dimetilpropila, 1,2-dimetilpropila, 1-metilpentila, 2- metilpentila, 3-metilpentila, 4-metilpentila, 1,1-dimetilbutila, 1,2- dimetilbutila, 1,3-dimetilbutila, 2,2-dimetilbutila, 2,3-dimetilbutila, 3,3- dimetilbutila, 1-etilbutila, 2-etilbutila, 1,1,2-trimetilpropila, 1,2,2- trimetilpropila, 1-etil-1-metilpropila e 1-etil-2-metilpropila.
[0018] Alquil halogênio-substituído significa grupos alquil de cadeia linear ou ramificada onde alguns ou todos os átomos de hidrogênio nesses grupos podem ser substituídos por átomos de halogênio, por exemplo, C1-C2-haloalquil tal como clorometila, bromometila, diclorometila, triclorometila, fluorometila, difluorometila, trifluorometila, clorofluorometila, diclorofluorometila, clorodifluorometila, 1-cloroetila, 1- bromoetila, 1-fluoroetila, 2-fluoroetila, 2,2-difluoroetila, 2,2,2- trifluoroetila, 2-cloro-2-fluoroetila, 2-cloro-2-difluoroetila, 2,2-dicloro-2- fluoroetila, 2,2,2-tricloroetila, pentafluoroetila e 1,1,1-trifluoroprop-2-ila.
[0019] Alquenil significa radicais hidrocarbil insaturado de cadeia linear ou ramificada tendo o número de átomos de carbono especificado em cada caso e uma ligação dupla em qualquer posição, por exemplo, C2-C6-alquenil tal como etenila, 1-propenila, 2-propenila, 1-metiletenila, 1-butenila, 2-butenila, 3-butenila, 1-metil-1-propenila, 2- metil-1-propenila, 1-metil-2-propenila, 2-metil-2-propenila, 1-pentenila, 2-pentenila, 3-pentenila, 4-pentenila, 1-metil-1-butenila, 2-metil-1- butenila, 3-metil-1-butenila, 1-metil-2-butenila, 2-metil-2-butenila, 3- metil-2-butenila, 1-metil-3-butenila, 2-metil-3-butenila, 3-metil-3- butenila, 1,1-dimetil-2-propenila, 1,2-dimetil-1-propenila, 1,2-dimetil-2- propenila, 1-etil-1-propenila, 1-etil-2-propenila, 1-hexenila, 2-hexenila, 3-hexenila, 4-hexenila, 5-hexenila, 1-metil-1-pentenila, 2-metil-1- pentenila, 3-metil-1-pentenila, 4-metil-1-pentenila, 1-metil-2-pentenila, 2-metil-2-pentenila, 3-metil-2-pentenila, 4-metil-2-pentenila, 1-metil-3- pentenila, 2-metil-3-pentenila, 3-metil-3-pentenila, 4-metil-3-pentenila, 1-metil-4-pentenila, 2-metil-4-pentenila, 3-metil-4-pentenila, 4-metil-4- pentenila, 1,1-dimetil-2-butenila, 1,1-dimetil-3-butenila, 1,2-dimetil-1- butenila, 1,2-dimetil-2-butenila, 1,2-dimetil-3-butenila, 1,3-dimetil-1- butenila, 1,3-dimetil-2-butenila, 1,3-dimetil-3-butenila, 2,2-dimetil-3- butenila, 2,3-dimetil-1-butenila, 2,3-dimetil-2-butenila, 2,3-dimetil-3- butenila, 3,3-dimetil-1-butenila, 3,3-dimetil-2-butenila, 1-etil-1-butenila, 1-etil-2-butenila, 1-etil-3-butenila, 2-etil-1-butenila, 2-etil-2-butenila, 2- etil-3-butenila, 1,1,2-trimetil-2-propenila, 1-etil-1-metil-2-propenila, 1- etil-2-metil-1-propenila e 1-etil-2-metil-2-propenila.
[0020] Alquinil significa radicais hidrocarbil de cadeia linear ou ramificada tendo o número de átomos de carbono especificado em cada caso e uma ligação tripla em qualquer posição, por exemplo, C2- C6-alquinil tal como etinila, 1-propinila, 2-propinil (or propargil), 1- butinila, 2-butinila, 3-butinila, 1-metil-2-propinila, 1-pentinila, 2-pentinila, 3-pentinila, 4-pentinila, 3-metil-1-butinila, 1-metil-2-butinila, 1-metil-3- butinila, 2-metil-3-butinila, 1,1-dimetil-2-propinila, 1-etil-2-propinila, 1- hexinila, 2-hexinila, 3-hexinila, 4-hexinila, 5-hexinila, 3-metil-1-pentinila, 4-metil-1-pentinila, 1-metil-2-pentinila, 4-metil-2-pentinila, 1-metil-3- pentinila, 2-metil-3-pentinila, 1-metil-4-pentinila, 2-metil-4-pentinila, 3- metil-4-pentinila, 1,1-dimetil-2-butinila, 1,1-dimetil-3-butinila, 1,2- dimetil-3-butinila, 2,2-dimetil-3-butinila, 3,3-dimetil-1-butinila, 1-etil-2- butinila, 1-etil-3-butinila, 2-etil-3-butinila e 1-etil-1-metil-2-propinila.
[0021] Cicloalquil significa um sistema anelar carbocíclico saturado tendo de preferência 3-8 átomos de carbono no anel, por exemplo, ciclopropila, ciclobutila, ciclopentila ou ciclo-hexila. No caso de cicloalquil opcionalmente substituído, sistemas cíclicos com substituintes estão incluídos, incluindo também substituintes com uma ligação dupla no radical cicloalquila, por exemplo, um grupo alquilideno tal como metilideno.
[0022] No caso de cicloalquil opcionalmente substituído, sistemas policíclicos alifáticos também estão incluídos, por exemplo, biciclo[1.1.0]butan-1-ila, biciclo[1.1.0]butan-2-ila, biciclo[2.1.0]pentan-1- ila, biciclo[2.1.0]pentan-2-ila, biciclo[2.1.0]pentan-5-ila, biciclo[2.2.1]hept-2-il (norbornil), adamantan-1-ila e adamantan-2-ila.
[0023] No caso de cicloalquil substituído, sistemas espirocíclicos alifáticos também estão incluídos, por exemplo, espiro[2.2]pent-1-ila, espiro[2.3]hex-1-ila, espiro[2.3]hex-4-ila, 3-espiro[2.3]hex-5-ila.
[0024] Cicloalquenil significa um sistema anel carbocíclico, não aromático, parcialmente insaturado tendo de preferência 4-8 átomos de carbono, por exemplo, 1-ciclobutenila, 2-ciclobutenila, 1- ciclopentenila, 2-ciclopentenila, 3-ciclopentenila, ou 1-ciclo-hexenila, 2- ciclo-hexenila, 3-ciclo-hexenila, 1,3-ciclo-hexadienila ou 1,4-ciclo- hexadienila, incluindo também substituintes com uma ligação dupla no radical cicloalquenila, por exemplo, um grupo alquilideno tal como metilideno. No caso de cicloalquenil opcionalmente substituído, as explicações para cicloalquil substituído aplicam-se de forma correspondente.
[0025] Alcóxi significa radicais alcóxi saturado de cadeia linear ou ramificada tendo o número de átomos de carbono especificado em cada caso, por exemplo, C1-C6-alcóxi tal como metóxi, etóxi, propóxi, 1-metiletóxi, butóxi, 1-metilpropóxi, 2-metilpropóxi, 1,1-dimetiletóxi, pentóxi, 1-metilbutóxi, 2-metilbutóxi, 3-metilbutóxi, 2,2-dimetilpropóxi, 1-etilpropóxi, hexóxi, 1,1-dimetilpropóxi, 1,2-dimetilpropóxi, 1- metilpentóxi, 2-metilpentóxi, 3-metilpentóxi, 4-metilpentóxi, 1,1- dimetilbutóxi, 1,2-dimetilbutóxi, 1,3-dimetilbutóxi, 2,2-dimetilbutóxi, 2,3- dimetilbutóxi, 3,3-dimetilbutóxi, 1-etilbutóxi, 2-etilbutóxi, 1,1,2- trimetilpropóxi, 1,2,2-trimetilpropóxi, 1-etil-1-metilpropóxi e 1-etil-2- metilpropóxi. Alcóxi halogênio-substituído significa radicais alcóxi de cadeia linear ou ramificada tendo o número de átomos de carbono especificado em cada caso, onde alguns ou todos os átomos de hidrogênio nesses grupos podem ser substituídos por átomos de halogênio como especificado acima, por exemplo, C1-C2-haloalcóxi tal como clorometóxi, bromometóxi, diclorometóxi, triclorometóxi, fluorometóxi, difluorometóxi, trifluorometóxi, clorofluorometóxi, diclorofluorometóxi, clorodifluorometóxi, 1-cloroetóxi, 1-bromoetóxi, 1- fluoroetóxi, 2-fluoroetóxi, 2,2-difluoroetóxi, 2,2,2-trifluoroetóxi, 2-cloro- 2-fluoroetóxi, 2-cloro-1,2-difluoroetóxi, 2,2-dicloro-2-fluoroetóxi, 2,2,2- tricloroetóxi, pentafluoroetóxi e 1,1,1-trifluoroprop-2-óxi.
[0026] O termo "aril" denota um sistema aromático mono-, bi- ou policíclico opcionalmente substituído tendo de preferência 6 a 14, especialmente 6 a 10, átomos de carbono no anel, por exemplo, fenila, naftila, antrila, fenantrenila, entre outros, de preferência fenila.
[0027] O termo " aril opcionalmente substituído" também inclui sistemas policíclicos, tal como tetra-hidronaftila, indenila, indanila, fluorenila, bifenilila, onde o ponto de ligação fica no sistema aromático. Em termos sistemáticos, "aril" geralmente também está abrangido pelo termo "fenil opcionalmente substituído ".
[0028] As arilas elacionadas acima são de preferência substituídas, por exemplo, com hidrogênio, halogênio, alquila, haloalquila, hidroxila, alcóxi, cicloalcóxi, arilóxi, alcoxialquila, alcoxialcóxi, cicloalquila, halocicloalquila, arila, arilalquila, heteroarila, heterociclila, alquenila, alquil carbonila, cicloalquil carbonila, arilcarbonila, heteroarilcarbonila, alcoxicarbonila, hidroxicarbonila, cicloalcoxicarbonila, cicloalquil alcoxicarbonila, alcoxicarbonilalquila, arilalcoxicarbonila, arilalcoxicarbonilalquila, alquinila, alquinil alquila, alquil alquinila, trisalquil sililalquinila, nitro, amino, ciano, haloalcóxi, haloalquiltio, alquiltio, hidrotio, hidroxialquila, heteroarilalcóxi, arilalcóxi, heterociclilalcóxi, heterociclilalquiltio, heterociclilóxi, heterocicliltio, heteroarilóxi, bisalquilamino, alquilamino, cicloalquilamino, hidroxicarbonilalquilamino, alcoxicarbonilalquilamino, arilalcoxicarbonilalquilamino, alcoxicarbonilalquil (alquil)amino, aminocarbonila, alquilaminocarbonila, bisalquilaminocarbonila, cicloalquilaminocarbonila, hidroxicarbonilalquilaminocarbonila, alcoxicarbonilalquilaminocarbonila, arilalcoxicarbonilalquilaminocarbonila.
[0029] O termo "halogênio" significa flúor, cloro, bromo ou iodo. Se o termo for usado para um radical, "halogênio" significa um átomo de flúor, cloro, bromo ou iodo.
[0030] De acordo com a natureza dos substituintes e a forma como eles são unidos, os compostos de Fórmula (I) podem estar presentes como estereoisômeros. Se, por exemplo, um ou mais átomos de carbono assimetricamente substituídos e/ou sulfóxidos estiverem presentes, podem ocorrer enantiômeros e diastereômeros. Estereoisômeros podem ser obtidos a partir das misturas obtidas na preparação por métodos de separação usuais, por exemplo, por processos de separação cromatográfica. É igualmente possível preparar estereoisômeros de forma seletiva por meio de reações estereosseletivas usando materiais de partida e/ou auxiliares oticamente ativos.
[0031] A invenção também se refere a todos os estereoisômeros e misturas dos mesmos que são abrangidos pela Fórmula (I), mas que não estão definidos de forma específica. No entanto, o texto a seguir, por simplicidade, mencionará sempre compostos de Fórmula (I), embora fique entendido que isto significa não apenas os compostos puros, mas também, onde apropriado, misturas com várias quantidades de compostos isoméricos.
[0032] De acordo com a natureza dos substituintes definidos acima, os compostos de Fórmula (I) possuem propriedades ácidas e podem formar sais, se apropriado também sais internos ou adutos, com bases inorgânicas ou orgânicas ou com íons metálicos. Se os commposto de Fórmula (I) carregarem grupos hidroxila, carboxila ou outros grupos que induzem propriedades ácidas, esses compostos ser reagidos com bases para dar sais. Bases adequadas são, por exemplo, hidróxidos, carbonatos, bicarbonatos de metais alcalinos e metais alcalino-terrosos, em particular aqueles de sódio, potássio, magnésio e cálcio, e ainda amônia, aminas primárias, secundárias e terciárias tendo grupos (C1-C4)-alquila, mono-, di- e trialcanolaminas de (C1-C4)-alcanóis, colina e clorocolina, e também aminas orgânicas tal como trialquilaminas, morfolina, piperidina ou piridina. Estes sais são compostos nos quais o hidrogênio ácido é substituído por um cátion agricolamente adequado, por exemplo, sais metálicos, especialmente sais de metais alcalinos ou sais de metais alcalino- terrosos, em particular sais de sódio e de potássio, ou ainda sais de amônio, sais com aminas orgânicas ou sais de amônio quaternário, por exemplo, com cátions de fórmula [NRR'R"R"']+ na qual R a R'" cada um independentemente do outro representam um radical orgânico, em particular alquila, arila, aralquila ou alquilarila. Também adequados são sais de alquilsulfônio e alquilsulfoxônio, tal como sais de (C1-C4)-trialquilsulfônio e de (C1-C4)-trialquilsulfoxônio. Os compostos de Fórmula (I) podem formar adição por adição de um ácido inorgânico ou orgânico adequado, por exemplo, ácidos minerais, por exemplo, HCl, HBr, H2SO4, H3PO4 ou HNO3, ou ácidos orgânicos, por exemplo, ácidos carboxílicos tal como ácido fórmico, ácido acético, ácido propiônico, ácido oxálico, ácido láctico ou ácido salicílico ou ácidos sulfônicos, por exemplo, ácido p-toluenossulfônico, a um grupo básico, por exemplo, amino, alquilamino, dialquilamino, piperidino, morfolino ou piridino. Neste caso, estes sais compreendem a base conjugada do ácido como o ânion.
[0033] Substituintes adequados presentes na forma desprotonada, tal como, por exemplo, ácidos sulfônicos ou ácidos carboxílicos, podem formar sais internos com grupos que, por sua vez, podem ser protonados, tal como grupos amino.
[0034] Se um grupo for polissubstituído com radicais, isto significa que este grupo é substituído com um ou mais radicais idênticos ou diferentes daqueles mencionados.
[0035] Em todas as fórmulas especificadas a seguit, os substituintes e os símbolos têm o mesmo significado que aquele descrito na Fórmula Geral (I) dos herbicidas (A), a menos que indicado em contrário. As setas em uma fórmula química representam os pontos nos quais ela é unida ao resto da molécula.
[0036] A seguir, significados preferidos, particularmente preferidos e muito particularmente preferidos estão descritos para cada um dos substituintes individuais dos herbicidas (A) de acordo com a Fórmula Geral (I), mostrada acima. Os outros substituintes dos herbicidas (A) de Fórmula Geral (I) que não estiverem especificados abaixo têm a definição dada acima.
[0037] Em uma primeira modalidade da presente invenção, R3 de preferência representa (C1-C3)-alquila, (C2-C3)- alquenila ou (C1-C3)-alcóxi, cada um deles substituído com m radicais do grupo que consiste em flúor e cloro.
[0038] Particularmente de preferência, R3 representa metila, vinila, trifluorometila ou metóxi.
[0039] Em uma segunda modalidade da presente invenção, R11, R12 independentemente um do outro representam hidrogênio, ciano, OR7, S(O)n R5, CO2R8, COR6, NR6R8, NR6COR8, ou representam (C1-C6)-alquila, (C3-C6)-cicloalquila, (C3-C6)- cicloalquil -(C1-C3)-alquila, (C2-C6)-alquenila ou (C2-C6)-alquinila, cada um deles opcionalmente substituído com m radicais do grupo que consiste em halogênio, ciano, OR7, S(O)nR5, CO2R8, ou R11 e R 12 junto com o átomo de nitrogênio ao qual eles estão presos formam um anel saturado, parcialmente ou totalmente insaturado de cinco, seis ou sete membros que é opcionalmente mono- a hexassubstituído com radicais do grupo que consiste em halogênio, ciano, (C1-C6)-alquila, halo-(C1-C6)-alquila, oxo, OR7, S(O)n R5, CO2R8, e que, além deste átomo de nitrogênio, contém r átomos de carbono, n átomos de oxigênio, p átomos de enxofre e p elementos do grupo que consiste em NR7 e NCOR7 como átomos do anel.
[0040] Mais preferivelmente, R11, R12 independentemente um do outro representam hidrogênio, ciano, OR7, S(O)n R5, ou representam (C1-C3)-alquil opcionalmente substituído em cada caso com m radicais do grupo que consiste em halogênio, OR7, S(O)nR5.
[0041] Em uma terceira modalidade da presente invenção, R5 representa (C1-C6)-alquil substituído em cada caso com m radicais do grupo que consiste em halogênio e ciano.
[0042] Mais preferivelmente, R5 representa (C1-C3)-alquil substituído em cada caso com m radicais do grupo que consiste em halogênio e ciano.
[0043] Ainda mais preferivelmente, R5 representa (C1-C3)-alquil substituído em cada caso com m radicais do grupo que consiste em flúor, cloro e bromo.
[0044] Em uma quarta modalidade da presente invenção, R7 representa hidrogênio, ou representa (C1-C6)-alquila, (C3-C4)-alquenila ou (C3-C4)- alquinila, cada um deles substituído com m radicais do grupo que consiste em halogênio, ciano e (C1-C2)-alcóxi.
[0045] Mais preferivelmente, R7 representa hidrogênio, ou representa (C1-C3)-alquila ou (C3-C4)-alquenila, cada um deles substituído com m radicais do grupo que consiste em halogênio, ciano e (C1-C2)-alcóxi.
[0046] Ainda mais preferivelmente, R7 representa hidrogênio, ou representa (C1-C3)-alquil substituído em cada caso com m radicais do grupo que consiste em flúor, cloro e bromo.
[0047] Em uma quinta modalidade da presente invenção, R8 representa hidrogênio, ou representa (C1-C6)-alquila, (C3-C6)-alquenila ou (C3-C6)- alquinila, cada um deles substituído com m radicais do grupo que consiste em halogênio e (C1-C2)-alcóxi.
[0048] Mais preferivelmente, R8 representa hidrogênio, ou representa (C1-C3)-alquila ou (C3-C4)-alquenila, cada um deles substituído com m radicais do grupo que consiste em halogênio e (C1-C2)-alcóxi.
[0049] Em uma sexta modalidade da presente invenção, Z de preferência representa o grupo Z-1 ou Z13, onde Z- 1 e Z13 têm o seguinte significado: onde a seta em cada caso denota uma ligação ao grupo C=O de Fórmula (I).
[0050] Em uma sétima modalidade da presente invenção, X2, X4 e X6 representam, cada um, hidrogênio.
[0051] No contexto da presente invenção, os significados preferidos, mais preferidos e ainda mais preferidos individuais para os substituintes R3, R5 a R8, R11, R12, X2 a X6 e Z podem ser combinados entre si conforme desejado.
[0052] Isto significa que a presente invenção abrange herbicidas (A) de Fórmula Geral (I) na qual, por exemplo, o substituinte R3 tem um significado preferidos e os substituintes R5 a R8 têm um significa genérico ou ainda o substituinte R5 tem um significado preferido, o substituinte R11 tem um significado particularmente preferido ou muito particularmente preferido e os demais substituintes têm um significado genético.
[0053] Duas dessas combinações das definições dadas acima para os substituintes R3, R5 a R8, R11, R12, X2 a X6 e Z estão ilustradas abaixo a título de exemplo, e cada uma delas é revelada como uma modalidade adicional:
[0054] Em uma oitava modalidade da presente invenção, R1 e R 2 representam, cada um, hidrogênio; R3 representa (C1-C3)-alquila, (C2-C3)-alquenila ou (C1- C3)-alcóxi, cada um deles substituído com m radicais do grupo que consiste em flúor e cloro; R11, R12 independentemente um do outro representam hidrogênio, ciano, OR7, S(O)n R5, CO2R8, ou representam (C1-C3)-alquila ou (C2-C6)-alquenila, cada um deles opcionalmente substituído com m radicais do grupo que consiste em halogênio, ciano, OR7, S(O)nR5; R5 representa (C1-C3)-alquil substituído em cada caso com m radicais do grupo que consiste em halogênio e ciano; R6 representa hidrogênio ou R5; R7 representa hidrogênio, ou representa (C1-C3)-alquila ou (C3-C4)-alquenila, cada um deles substituído com m radicais do grupo que consiste em halogênio, ciano e (C1-C2)-alcóxi; R8 representa hidrogênio, ou representa (C1-C3)-alquila ou (C3-C4)-alquenila, cada um deles substituído com m radicais do grupo que consiste em halogênio e (C1-C2)-alcóxi; Z representa o grupo Z-1 or Z-13, onde Z-1 e Z-13 têm o seguinte significado: onde a seta em cada caso denota uma ligação ao grupo C=O de Fórmula (I); X2, X4 e X6 representam, cada um, hidrogênio; X3 e X5 independentemente um do outro representam hidrogênio, flúor, cloro ou ciano, ou representam (C1-C3)-alquila ou (C1-C3)-alcóxi, cada um deles substituído com m radicais do grupo que consiste em flúor e cloro; m o índice é 0, 1, 2 ou 3; e n o índice é 0, 1 ou 2.
[0055] Em uma nona modalidade da presente invenção, R1 e R 2 representam, cada um, hidrogênio; R3 representa metila, vinila, trifluorometila ou metóxi; R11, R12 independentemente um do outro representam hidrogênio, ciano, OR7, S(O)n R5, ou representam (C1-C3)-alquil opcionalmente substituído em cada caso com m radicais do grupo que consiste em halogênio, OR7, S(O)nR5; R5 representa (C1-C3)-alquil substituído em cada caso com m radicais do grupo que consiste em flúor, cloro e bromo; R6 representa hidrogênio ou R5; R7 representa hidrogênio, ou representa (C1-C3)-alquil substituído em cada caso com m radicais do grupo que consiste em flúor, cloro e bromo; Z representa o grupo Z-1 ou Z-13, onde Z-1 e Z-13 têm o seguinte significado: onde a seta em cada caso denota uma ligação ao grupo C=O de Fórmula (I); X2, X4 e X6 representam, cada um, hidrogênio; X3 e X5 independentemente um do outro representam hidrogênio, flúor, cloro ou ciano, ou representam (C1-C3)-alquila ou (C1-C3)-alcóxi, cada um deles substituído com m radicais do grupo que consiste em flúor e cloro; m o índice é 0, 1, 2 ou 3; e n o índice é 0, 1 ou 2.
[0056] Em uma décima modalidade da presente invenção, a composição herbicida, assim como pelo menos um componente (B) definido acima, de preferência compreende (A) um ou mais compostos [componente (A)] de Fórmula Geral (I) ou sais agroquimicamente compatíveis dos mesmos [herbicidas (A)] de acordo com as Tabelas 1a e 1b. Tabela 1a: Compostos de Fórmula (I) preferidos (herbicida (A)):
Tabela 1b: Nomes IUPAC e fórmulas estruturais dos compostos de Fórmula (I) preferidos (herbicida (A)):
[0057] A expressão rel-(2R,4R) está de acordo com a nomenclatura IUPAC, e significa que ambas as configurações cis dos substituintes nas posições 2 e 4 existem.
[0058] Nas Tabelas 1a e 1b, os compostos estão identificados pela fórmula química do componente principal, este componente estando presente em uma pureza química de preferência de pelo menos 95 por cento em peso do composto. Os compostos naturalmente também podem ser usados com purezas mais baixas. Especialmente quando os componentes secundários dos compostos consistem totalmente ou predominantemente em estereoisômeros dos respectivos compostos (A), as eficácias são atingidas na aplicação. Herbicidas (A) preferidos também são, portanto, misturas de dois ou mais compostos (A) de acordo com a invenção.
[0059] Quando a orientação estereoquímica em um átomo de carbono está definida nas Tabelas 1a e 1b, o componente principal do composto é um estereoisômero ou mistura de estereoisômeros tendo a configuração R ou S no átomo de carbono em questão.
[0060] Se nenhuma estereoquímica estiver definida, o composto é um racemato. Se houver múltiplos estereocentros e a configuração de cada um deles estiver identificada como R ou S, os compostos apresentam a estereoquímica indicada nos centros em questão.
[0061] Se não houver nenhuma configuração R ou S especificada para múltiplos centros, os compostos são misturas racêmicas, i.e., estereoisômeros de imagens especulares (enantiômeros de um par de enantiômeros) ali presentes estão presentes em proporções iguais na mistura. A menos que especificamente indicado, nas Tabelas 1a e 1b, os componentes diastereoméricos estão presentes em proporções aproximadamente iguais no caso de compostos racêmicos (A) com múltiplo estereocentros. Para uso prático, no entanto, existem misturas de diastereômeros com diferentes proporções dos componentes diastereoméricos no caso de compostos racêmicos com múltiplso estereocentros.
[0062] É preferível aqui que os respectivos compostos listados também estejam presentes em uma estereoquímica de 60% a 100%, de preferência 70-100%, especialmente 80% a 100%.
[0063] Dá-se preferência às misturas detalhadas de compostos estereoisoméricos (A).
[0064] Os compostos de Fórmula (I) são conhecidos através da referência PCT/EP2018/065334, que ainda estava para ser publicada na data de prioridade do presente pedido, e podem ser preparados pelos processos descritos naquela referência.
[0065] As taxas de aplicação dos herbicidas (A) variam na faixa de 0,01 a 2000 g de substância ativa por hectare (doravante, g i.a./ha), de preferência 0,02 a 1000 g i.a./ha, especialmente 0,5 a 750 g i.a./ha. Nas combinações de acordo com a invenção, no escopo das taxas de aplicação mencionadas em comparação a uma apliação individual, normalmente são necessárias taxas de aplicação mais baixas do respectivo composto ativo, de preferência 0,01 a 1000 g i.a./ha, especialmente 0,02 a 500 g i.a./ha, e ainda mais preferivelmente 5 a 250 g i.a./ha.
[0066] Parceiros (B) de combinação adequados [= componente (B) ou herbicidas (B)] são em princípio todos os compostos ativos dos subgrupos (B1) a (B11), onde os compostos herbicidas ativos estão largamente apresentados por seu nome comum (na terminologia em inglês) de acordo com a referência "The Pesticide Manual" 14th Ed., British Crop Protection Council 2006, abreviado "PM", ou pelo nome químico de acordo com as nomenclaturas padrão (IUPAC ou Chemical Abstracts).
[0067] No entanto, foi constatado que alguns herbicidas (B) são parceiros de combinação particularmente bons. Os herbicidas (B) preferidos, particularmente preferidos e mais preferidos estão listados a seguir como modalidades adicionais da presente invenção.
[0068] Em uma décima primeira modalidade da presente invenção, dá-se preferência aos compostos herbicidas ativos (B1): (B1.2) biciclopiirona, (B1.7) mesotriona, (B1.8) pinoxaden, (B1.10) setoxidim, (B1.11) sulcotriona, (B1.14) tembotriona e (B1.16) tralcoxidim.
[0069] Dá-se preferência particular aos compostos herbicidas ativos (B1.7) mesotriona e (B1.8) pinoxaden.
[0070] Em uma décima segunda modalidade da presente invenção, dá-se preferência aos compostos herbicidas ativos (B2): (B2.3) amidosulfuron, (B2.4) asulam, (B2.6) beflubutamid, (B2.10) clorimuron, (B2.12) clorsulfuron, (B2.14) cloransulam, (B2.17) diclosulam, (B2.18) diflufenican, (B2.23) etoxisulfuron, (B2.24) flazasulfuron, (B2.25) florasulam, (B2.26) flucarbazona, (B2.28) flufenacet, (B2.29) flumetsulam, (B2.30) flupirsulfuron, (B2.34) iodosulfuron, (B2.37) mesosulfuron, (B2.40) metolaclor, (B2.41) metosulam, (B2.42) metsulfuron, (B2.46) penoxsulam, (B2.49) picolinafen, (B2.56) propoxicarbazona, (B2.59) prosulfocarb, (B2.60) prosulfuron, (B2.62) piroxsulam, (B2.63) rimsulfuron, (B2.64) S-metolaclor, (B2.65) sulfometuron, (B2.66) sulfosulfuron, (B2.68) tiencarbazona, (B2.69) tifensulfuron, (B2.72) tribenuron, (B2.76) esprocarb, (B2.78) triallate.
[0071] Dá-se preferência particular a (B2.18) diflufenican, (B2.25) florasulam, (B2.28) flufenacet, (B2.37) mesosulfuron, (B2.40) metolaclor, (B2.63) rimsulfuron e (B2.68) tiencarbazona.
[0072] Em uma décima terceira modalidade da presente invenção, dá-se preferência aos compostos herbicidas ativos (B3) (B3.1) bromoxinil e (B3.4) ioxinila.
[0073] Em uma décima quarta modalidade da presente invenção, dá-se preferência aos compostos herbicidas ativos (B4): (B4.2) amitrole, (B4.8) carfentrazona, (B4.10) imazametabenz, (B4.11) imazamox, (B4.12) imazapic, (B4.13) imazapir, (B4.15) imazetapir, (B4.17) isoxaben, (B4.18) isoxaflutole, (B4.21) piraflufen, (B4.22) pirasulfotole, (B4.25) piroxasulfona, (B4.28) topramezona, e (B4.33) flupoxam.
[0074] Dá-se preferência particular a (B4.18) isoxaflutole, (B4.22) pirasulfotole e (B4.25) piroxasulfona.
[0075] Em uma décima quinta modalidade da presente invenção, dá-se preferência aos compostos herbicidas ativos (B5): (B5.1) aminociclopiraclor, (B5.2) aminopiralid, (B5.3) benazolin, (B5.5) bentazona, (B5.7) bixlozona, (B5.12) cinidon, (B5.13) cinmetilin, (B5.14) clomazona, (B5.21) etofumesato, (B5.22) flamprop, (B5.23) florpirauxifen, (B5.26) flumioxazin, (B5.27) fluridona, (B5.28) flurocloridona, (B5.29) flurtamona, (B5.31) halauxifen, (B5.32) indanofan, (B5.37) paraquat, (B5.38) ácido pelargonico, (B5.39) pendimetalin, (B5.45) triafamona e (B5.46) trifluralin, (B5.47) 4-amino-3-cloro-5-fluoro-6-(7- fluoro-1H-indol-6-il)piridine-2- ácido carboxilico, (B5.48) ciclopirimorate, (B5.49) diquat, (B5.50) oxaziclomefona.
[0076] Dá-se preferência particular a (B5.7) bixlozona, (B5.23) florpirauxifen, (B5.31) halauxifen e (B5.38) ácido pelargonico.
[0077] Em uma décima sexta modalidade da presente invenção, dá-se preferência aos compostos herbicidas ativos (B6): (B6.2) clopiralid, (B6.3) dicamba, (B6.4) fluroxipir e (B6.5) picloram.
[0078] Dá-se preferência particular a (B6.2) clopiralid, (B6.3) dicamba e (B6.4) fluroxipir.
[0079] Em uma décima sétima modalidade da presente invenção, dá-se preferência aos compostos herbicidas ativos (B7): (B7.2) bialafos, (B7.4) glufosinato, (B7.5) glifosato e (B7.7) sulfosato.
[0080] Dá-se preferência particular a (B7.5) glifosato e (B7.7) sulfosato.
[0081] Em uma décima oitava modalidade da presente invenção, dá-se preferência aos compostos herbicidas ativos (B8): (B8.1) 2,4-D, (B8.3) 2,4-DP, (B8.5) aclonifen, (B8.8) clodinafop, (B8.11) diclofop, (B8.13) fenoxaprop, (B8.20) MCPA, (B8.22) mecoprop, (B8.26) quizalofop e (B8.27) quizalofop.
[0082] Dá-se preferência particular a (B8.1) 2,4-D e (B8.5) aclonifen.
[0083] Em uma décima nona modalidade da presente invenção, dá-se preferência aos compostos herbicidas ativos (B9): (B9.10) saflufenacila, (B9.11) terbacil, (B9.13) trifludimoxazin e (B9.14) etil [3-[2-cloro-4-fluoro-5-(1-metil-6-trifluorometil- 2,4-dioxo-1,2,3,4-tetrahidropirimidin-3-il)fenoxi]- 2-piridiloxi]acetate.
[0084] Dá-se mais preferência a (B9.10) saflufenacila.
[0085] Em uma vigésima modalidade da presente invenção, dá-se preferência aos compostos herbicidas ativos (B10): (B10.1) clorobromuron, (B10.2) clorotoluron, (B10.5) diuron, (B10.8) isoproturon, (B10.9) linuron, (B10.10) metabenztiazuron, (B10.11) metobromuron, (B10.12) metoxuron e (B10.13) monolinuron.
[0086] Dá-se preferência particular a (B10.5) diuron e (B10.8) isoproturon.
[0087] Em uma vigésima primeira modalidade da presente invenção, dá-se preferência aos compostos herbicidas ativos (B11): (B11.1) ametrine, (B11.2) atrazine, (B11.5) hexazinona, (B11.6) indaziflam, (B11.8) metribuzin, (B11.12) simazine, (B11.15) terbutilazine e (B11.16) terbutrine.
[0088] Dá-se preferência particular a (B11.5) hexazinona, (B11.6) indaziflam e (B11.8) metribuzin.
[0089] No contexto da presente invenção, é possível combinar as modalidades preferidas, particularmente preferidas e mais preferidas individuais umas com as outras, conforme desejado. Isto significa que composições herbicidas compreendendo (A) um ou mais compostos de Fórmula Geral (I) ou sais agroquimicamente compatíveis dos mesmos [componente (A)] e (B) um ou mais herbicidas [componente (B)] selecionados do grupo dos compostos herbicidas ativos (B1) a (B11) estão abrangidas pela presente invenção, onde quaisquer modalidades reveladas preferidas, particularmente preferidas e mais preferidas desejadas podem ser combinadas umas com as outras, como detalhado acima.
[0090] Foi surpreendentemente constatado que algumas composições binárias compreendendo (A) um ou mais compostos herbicidamente ativos (A) de Fórmula Geral (I) ou sais agroquimicamente compatíveis dos mesmos [herbicidas (A)] e um herbicida (B) são particularmente vantajosas. Os sistemas binários preferidos, particularmente preferidos e mais preferidos estão listados a seguir como molidades adicionais da presente invenção.
[0091] Em uma vigésima segunda modalidade da presente invenção, a composição de preferência compreende (A) um composto de Fórmula Geral (I) ou sais agroquimicamente compatíveis dos mesmos [herbicidas (A)] na qual R1 e R 2 representam, cada um, hidrogênio; R3 representa (C1-C3)-alquila, (C2-C3)-alquenila ou (C1- C3)-alcóxi, cada um deles substituído com m radicais do grupo que consiste em flúor e cloro; R11, R12 independentemente um do outro representam hidrogênio, ciano, OR7, S(O)n R5, CO2R8, ou representam (C1-C3)-alquila ou (C2-C6)-alquenila, cada um deles opcionalmente substituído com m radicais do grupo que consiste em halogênio, ciano, OR7, S(O)nR5; R5 representa (C1-C3)-alquil substituído em cada caso com m radicais do grupo que consiste em halogênio e ciano; R6 representa hidrogênio ou R5; R7 representa hidrogênio, ou representa (C1-C3)-alquila ou (C3-C4)-alquenila, cada um deles substituído com m radicais do grupo que consiste em halogênio, ciano e (C1-C2)-alcóxi; R8 representa hidrogênio, ou representa (C1-C3)-alquila ou (C3-C4)-alquenila, cada um deles substituído com m radicais do grupo que consiste em halogênio e (C1- C2)-alcóxi; Z representa o grupo Z-1 ou Z-13, onde Z-1 e Z-13 têm o seguinte significado: onde a seta em cada caso denota uma ligação ao grupo C=O de Fórmula (I); X2, X4 e X6 representam, cada um, hidrogênio; X3 e X5 independentemente um do outro representam hidrogênio, flúor, cloro ou ciano, ou representam (C1-C3)-alquila ou (C1-C3)-alcóxi, cada um deles substituído com m radicais do grupo que consiste em flúor e cloro; m o índice é 0, 1, 2 ou 3; e n o índice é 0, 1 ou 2; e (B) um herbicida [componente (B)] do grupo que consiste em (B1.(2) biciclopiirona, (B1.(7) mesotriona, (B1.(8) pinoxaden, (B1.(10) setoxidim, (B1.(11) sulcotriona, (B1.(14) tembotriona, (B1.(16) tralcoxidim; (B1.(17) amidosulfuron, (B1.(18) asulam, (B2.(6) beflubutamid, (B2.10) clorimuron, (B2.12) clorsulfuron, (B2.14) cloransulam, (B2.17) diclosulam, (B2.18) diflufenican, (B2.23) etoxisulfuron, (B2.24) flazasulfuron, (B2.25) florasulam, (B2.26) flucarbazona, (B2.28) flufenacet, (B2.29) flumetsulam, (B2.30) flupirsulfuron, (B2.34) iodosulfuron, (B2.37) mesosulfuron, (B2.40) metolaclor, (B2.41) metosulam, (B2.42) metsulfuron, (B2.46) penoxsulam, (B2.49) picolinafen, (B2.56) propoxicarbazona, (B2.59) prosulfocarb, (B2.60) prosulfuron, (B2.62) piroxsulam, (B2.63) rimsulfuron, (B2.64) S-metolaclor, (B2.65) sulfometuron, (B2.66) sulfosulfuron, (B2.68) tiencarbazona, (B2.69) tifensulfuron, (B2.72) tribenuron, (B2.76) esprocarb, (B2.78) triallate; (B3.1) bromoxinil, (B3.4) ioxinil; (B4.2) amitrole, (B4.8) carfentrazona, (B4.10) imazametabenz, (B4.11) imazamox, (B4.12) imazapic, (B4.13) imazapir, (B4.15) imazetapir, (B4.17) isoxaben, (B4.18) isoxaflutole, (B4.21) piraflufen, (B4.22) pirasulfotole, (B4.25) piroxasulfona, (B4.28) topramezona, (B4.33) flupoxam; (B5.1) aminociclopiraclor, (B5.2) aminopiralid, (B5.3) benazolin, (B5.5) bentazona, (B5.7) bixlozona, (B5.12) cinidon, (B5.13) cinmetilin, (B5.14) clomazona, (B5.21) etofumesato, (B5.22) flamprop, (B5.23) florpirauxifen, (B5.26) flumioxazin, (B5.27) fluridona, (B5.28) flurocloridona, (B5.29) flurtamona, (B5.31) halauxifen, (B5.32) indanofan, (B5.37) paraquat, (B5.38) ácido pelargonico, (B5.39) pendimetalin, (B5.45) triafamona, (B5.46) trifluralin, (B5.47) 4-amino-3-cloro-5-fluoro-6-(7- fluoro-1H-indol-6-il)piridine-2- ácido carboxilico, (B5.48) ciclopirimorate, (B5.49) diquat, (B5.50) oxaziclomefona; (B6.2) clopiralid, (B6.3) dicamba, (B6.4) fluroxipir, (B6.5) picloram; (B7.2) bialafos, (B7.4) glufosinato, (B7.5) glifosato, (B7.7) sulfosato; (B8.1) 2,4-D, (B8.3) 2,4-DP, (B8.5) aclonifen, (B8.8) clodinafop, (B8.11) diclofop, (B8.13) fenoxaprop, (B8.20) MCPA, (B8.22) mecoprop, (B8.26) quizalofop, (B8.27) quizalofop; (B9.10) saflufenacila, (B9.11) terbacil, (B9.13) trifludimoxazin; (B10.1) clorobromuron, (B10.2) clorotoluron, (B10.5) diuron, (B10.8) isoproturon, (B10.9) linuron, (B10.10) metabenztiazuron, (B10.11) metobromuron, (B10.12) metoxuron, (B10.13) monolinuron; (B11.1) ametrine, (B11.2) atrazine, (B11.5) hexazinona, (B11.6) indaziflam, (B11.8) metribuzin, (B11.12) simazine, (B11.15) terbutilazine e (B11.16) terbutrine.
[0092] Em uma vigésima terceira modalidade da presente invenção, a composição de preferência compreende (A) um composto de Fórmula Geral (I) ou sais agroquimicamente compatíveis dos mesmos [herbicidas (A)] na qual R1 e R 2 representam, cada um, hidrogênio; R3 representa metila, vinila, trifluorometil or metóxi; R11, R12 independentemente um do outro representam hidrogênio, ciano, OR7, S(O)n R5, ou representam (C1-C3)-alquil opcionalmente substituído em cada caso com m radicais do grupo que consiste em halogênio, OR7, S(O)nR5; R5 representa (C1-C3)-alquil substituído em cada caso com m radicais do grupo que consiste em flúor, cloro e bromo; R6 representa hidrogênio ou R5; R7 representa hidrogênio, ou representa (C1-C3)-alquil substituído em cada caso com m radicais do grupo que consiste em flúor, cloro e bromo; Z representa o grupo Z-1 ou Z-13, onde Z-1 e Z-13 têm o seguinte significado: onde a seta em cada caso denota uma ligação ao grupo C=O de Fórmula (I); X2, X4 e X6 representam, cada um, hidrogênio; X3 e X5 independentemente um do outro representam hidrogênio, flúor, cloro ou ciano, ou representam (C1-C3)-alquila ou (C1-C3)-alcóxi, cada um deles substituído com m radicais do grupo que consiste em flúor e cloro; m o índice é 0, 1, 2 ou 3; e n o índice é 0, 1 ou 2; e (B) um herbicida [componente (B)] do grupo que consiste em (B1.7) (B1.8) mesotriona, pinoxaden, (B2.18) diflufenican, (B2.25) florasulam, (B2.28) flufenacet, (B2.37) mesosulfuron, (B2.40) metolaclor, (B2.63) rimsulfuron e (B2.68) tiencarbazona, (B4.18) isoxaflutole, (B4.22) pirasulfotole, (B4.25) piroxasulfona, (B5.7) bixlozona, (B5.23) florpirauxifen, (B5.38) ácido pelargonico, (B6.2) clopiralid, (B6.3) dicamba, (B6.4) fluroxipir, (B7.5) glifosato, (B7.7) sulfosato; (B8.1) 2,4-D, (B8.5) aclonifen, (B9.10) saflufenacila, (B10.5) diuron, (B10.8) isoproturon, (B11.5) hexazinona, (B11.6) indaziflam, (B11.8) metribuzin.
[0093] Composições particularmente preferidas no contexto da presente invenção são as composições relacionadas nas Tabelas 2.1 - 2.5 abaixo: Tabela 2.1: Composições binárias particularmente preferidas compreendendo (A1)
Tabela 2.2: Composições binárias particularmente preferidas compreendendo (A2)
Tabela 2.3: Composições binárias particularmente preferidas compreendendo (A3) Tabela 2.4: Composições binárias particularmente preferidas compreendendo (A4) Tabela 2.5: Composições binárias particularmente preferidas compreendendo (A5)
[0094] Além disso, as combinações de acordo com a invenção podem ser descritas junto com outros compostos ativos tal como os compostos ativos mencionados (herbicidas, fungicidas, inseticidas, acaricidas etc.) e/ou reguladores ou auxiliares do crescimento de plantas do grupo de aditivos usuais na proteção de lavouras, tal como adjuvantes e auxiliares de formulação. Aqui, a combinação de compostos protetores de lavouras ativos compreendendo os compostos ativos (A) e (B) e opcionalmente outros compostos ativos é denominada simplesmente “combinação herbicida”. Suas formas de uso tal como formulações ou misturas de tanque representam composições herbicidas.
[0095] Assim sendo, a invenção também apresenta composições herbicidas compreendendo as combinações de compostos ativos de acordo com a invenção com aditivos usuais na proteção de lavouras, tal como adjuvantrs e auxiliares de formulação, e opcionalmente outros compostos protetores de lavouras ativos.
[0096] A invenção também apresenta o uso das combinações de compostos ativos de acordo com a invenção ou o método de aplicação das mesmas como herbicidas e reguladores do crescimento de plantas, de preferência como herbicidas e reguladores do crescimento de plantas tendo um teor sinergisticamente ativo da combinação dos respectivos compostos ativos presentes.
[0097] As taxas de aplicação dos herbicidas (B) são em princípio conhecidos e geralmente variam na faixa de 0,01 a 4000 g i.a./ha, de preferência na faixa de 0.02 a 2000 g i.a./ha, em particular 0,1 a 2000 g i.a./ha. Para o composto ativo ácido pelargônico (B5.38) do grupo (B5), a taxa de aplicação varia na faixa de 1 a 100.000 g i.a./ha.
[0098] Nas misturas de acordo com a invenção, no contexto das taxas de aplicação mencionadas, geralmente são necessárias taxas de aplicação mais baixas dos respectivos compostos ativos em comparação com a aplicação individual.
[0099] Para os compostos ativos do grupo (B1), a taxa de aplicação varia de preferência na faixa de 5 a 250 g i.a./ha, em particular na faixa de 5 a 150 g i.a./ha e ainda mais preferivelmente na faixa de 5 a 60 g i.a./ha.
[00100] Para os compostos ativos do grupo (B2), a taxa de aplicação varia de preferência na faixa de 1 a 4000 g i.a./ha, em particular na faixa de 1 a 2000 g i.a./ha e ainda mais preferivelmente na faixa de 1 a 400 g i.a./ha.
[00101] Para o composto ativo do grupo (B3), a taxa de aplicação varia de preferência na faixa de 10 a 1000 g i.a./ha, em particular na faixa de 10 a 500 g i.a./ha e ainda mais preferivelmente na faixa de 10 a 300 g i.a./ha.
[00102] Para o composto ativo do grupo (B4), a taxa de aplicação varia de preferência na faixa de 1 a 700 g i.a./ha, em particular na faixa de 1 a 400 g i.a./ha e ainda mais preferivelmente na faixa de 1 a 200 g i.a./ha.
[00103] Para o composto ativo do grupo (B5), exceto para o ácido pelargônico (B5.38), a taxa de aplicação varia de preferência na faixa de 1 a 2400 g i.a./ha, em particular na faixa de 1 a 1200 g i.a./ha e ainda mais preferivelmente na faixa de 1 a 400 g i.a./ha. Para o ácido pelargônico (B.5.38), a taxa de aplicação varia de preferência de 1 a 100.000 g i.a./ha, mais preferivelmente 1 a 40,000 g i.a./ha e em particular na faixa de 1 a 30,000 g i.a./ha.
[00104] Para o composto ativo do grupo (B6), a taxa de aplicação varia de preferência na faixa de 10 a 1000 g i.a./ha, em particular na faixa de 10 a 600 g i.a./ha.
[00105] Para o composto ativo do grupo (B7), a taxa de aplicação varia de preferência na faixa de 20 a 3500 g i.a./ha, em particular na faixa de 20 a 2500 g i.a./ha e ainda mais preferivelmente na faixa de 20 a 2000 g i.a./ha.
[00106] Para o composto ativo do grupo (B8), a taxa de aplicação varia de preferência na faixa de 5 a 1500 g i.a./ha, em particular na faixa de 5 a 1000 g i.a./ha e ainda mais preferivelmente na faixa de 5 a 900 g i.a./ha.
[00107] Para o composto ativo do grupo (B9), a taxa de aplicação varia de preferência na faixa de 2 a 2000 g i.a./ha, em particular na faixa de 2 a 1000 g i.a./ha, mais preferivelmente na faixa de 2 a 200 g i.a./ha e ainda mais preferivelmente na faixa de 2 a 50 g i.a./ha.
[00108] Para o composto ativo do grupo (B10), a taxa de aplicação varia de preferência na faixa de 20 a 3500 g i.a./ha, em particular na faixa de 20 a 2000 g i.a./ha.
[00109] Para o composto ativo do grupo (B11), a taxa de aplicação varia de preferência na faixa de 25 a 3000 g i.a./ha, em particular na faixa de 25 a 2500 g i.a./ha e ainda mais preferivelmente na faixa de 25 a 2000 g i.a./ha.
[00110] As razões de (A):(B) com base no peso, dependendo das taxas de aplicação eficazes, geralmente variam na faixa de 1:100000 a 2000:1, de preferência 1:40000 a 750:1, especialmente na faixa de 1:15000 a 500:1 e ainda mais preferivelmente na faixa de 1:300 a 400:1.
[00111] Para os compostos ativos dos grupos (B1) a (B11), as razões em peso de (A):(B) preferidas são as seguintes: (A):(B1) de preferência na faixa de 30:1 a 1:30, em particular de 15:1 a 1:15; (A):(B2) de preferência na faixa de 400:1 a 1:400, em particular de 200:1 a 1:200; (A):(B3) de preferência na faixa de 30:1 a 1:30, em particular de 15:1 a 1:15; (A):(B4) de preferência na faixa de 300:1 a 1:300, em particular de 150:1 a 1:150; (A):(B5) de preferência na faixa de 400:1 a 1:300, em particular de 300:1 a 1:150; (A):(B6) de preferência na faixa de 60:1 a 1:60, em particular de 30:1 a 1:30; (A):(B7) de preferência na faixa de 10:1 a 1:200, em particular de 1:1 a 1:100; (A):(B8) de preferência na faixa de 30:1 a 1:300, em particular de 10:1 a 1:80; (A):(B9) de preferência na faixa de 80:1 a 1:200, em particular de 40:1 a 1:100; (A):(B10) de preferência na faixa de 10:1 a 1:300, em particular de 3:1 a 1:150; (A):(B11) de preferência na faixa de 30:1 a 1:300, em particular de 15:1 a 1:150.
[00112] As composições herbicidas de acordo com a invenção também podem ser combinadas com outros herbicidas e reguladores do crescimento de plantas, por exemplo, para complementar o espectro de atividade. Compostos ativos que podem ser descritos como parceiros de combinação para os compostos de acordo com a invenção em formulações mistas ou na mistura de tanque são, por exemplo, compostos ativos conhecidos que se baseiam na inibição da, por exemplo, acetolactato sintase, acetil-CoA carboxilase, celulose sintase, enolpiruvilshiquimato-3-fosfato sintase, glutamina sintetase, p- hidroxifenilpiruvate dioxigenase, fitoeno desaturase, fotossistema I, fotossistema II, protoporfirinogênio oxidase, conhecidos, por exemplo, através do documento Weed Research 26 (1986) 441-445 ou “The Pesticide Manual”, 14th edition, The British Crop Protection Council and the Royal Soc. of Chemistry, 2006, o “e-Pesticide Manual Version 4 (2006) correspondente” e a literatura ali citada. Outros nomes comerciais e “nomes comuns” estão listados no “Compendium of Pesticide Common Names” (disponível na Internet no endereço http://www.alanwood.net/pesticides).
[00113] Herbicidas conhecidos que podem ser mencionados como sendo adequados para serem combinados com os compostos de acordo com a invenção são, por exemplo, os seguintes compostos ativos (nota: os compostos estão apresentados seja pelo “nome comum” de acordo com a Organização Internacional para Padronização (ISO) ou pelo nome químico, se apropriado junto com número de código usual), e em todos os casos incluem todas as formas de uso, tal como ácidos, sais, ésteres e isômeros, tal como estereoisômeros e isômeros óticos. Neste caso, um ou ainda, em alguns casos, mais de uma forma de aplicação é mencionada:
[00114] 2,4-D, acetoclor, acifluorfen, acifluorfen sódico, aclonifen, alaclor, aloxidim, aloxidim sódico, ametryn, amicarbazona, amidosulfuron, amitrole, anilofos, asulam, atrazina, azafenidin, azimsulfuron, beflubutamid, benazolin, benazolin-etil, benfuresato, bensulfuron-metila, bentazona, benzfendizona, benzobiciclon, benzofenap, bifenox, bilanafos, bispiribac sódico, bromacila, bromobutida, bromofenoxim, bromoxinila, butaclor, butafenacila, butenaclor, butralin, butroxidim, butilato, cafenstrole, carbetamida, carfentrazona-etila, clometoxifeno, cloridazon, clorimuron-etila, clornitrofeno, clorotoluron, clorsulfuron, cinidon-etil, cinmetilina, cinosulfuron, clefoxidim, cletodim, clodinafop-propargila, clomazona, clomeprop, clopiralid, cloransulam-metila, cumiluron, cianazina, ciclosulfamuron, cicloxidim, cihalofop-butila, desmedifam, dicamba, diclobenila, diclorprop, diclorprop-P, diclofop-metila, diclosulam, difenzoquat, diflufenican, diflufenzopir, dikegulac sódico, dimefuron, dimepiperato, dimetaclor, dimetametrina, dimetenamida, triaziflam, diquat-dibrometo, ditiopir, diuron, dymron, EPTC, esprocarb, etalfluralin, etametsulfuron-metila, etoxifeno, etoxisulfuron, etobenzanid, fenoxaprop-etila, fenoxaprop-P-etila, fentrazamida, flamprop-M-isopropila, flamprop-M-metila, flazasulfuron, florasulam, fluazifop, fluazifop-butila, fluazolato, flucarbazona sódica, flucetosulfuron, flucloralin, flufenacet, flufenpir, flumetsulam, flumiclorac-pentila, flumioxazin, fluometuron, fluorocloridona, fluoroglicofen-etila, flupoxam, flupirsulfuron-metil sódico, fluridona, fluroxipir, fluroxipir-butoxipropila, fluroxipir-meptila, flurprimidol, flurtamona, flutiacet-metil, fomesafen, foramsulfuron, glufosinato, glufosinato-amônio, glifosato, halosulfuron-metila, haloxifop, haloxifop- etoxietila, haloxifop-metila, haloxifop-P-metila, hexazinona, imazametabenz-metila, imazamox, imazapic, imazapir, imazaquin, imazetapir, imazosulfuron, indanofan, iodosulfuron-metil sódico, ioxinila, isoproturon, isouron, isoxaben, isoxaclortole, isoxaflutole, ketospiradox, lactofeno, lenacila, linuron, MCPA, mecoprop, mecoprop- P, mefenacet, mesosulfuron-metila, mesotriona, metamifop, metamitron, metazaclor, metabenztiazuron, metildymron, metobromuron, metolaclor, metosulam, metoxuron, metribuzin, metsulfuron-metila, molinato, monolinuron, naproanilida, napropamida, neburon, nicosulfuron, norflurazon, orbencarb, oryzalin, oxadiargila, oxadiazon, oxasulfuron, oxaziclomefona, oxifluorfeno, paraquat, ácido pelargônico, pendimetalina, pendralina, pentoxazona, petoxamid, fenmedifam, picloram, picolinafen, pinoxaden, piperofos, pretilaclor, primisulfuron-metila, profluazol, profoxidim, prometrina, propaclor, propanila, propaquizafop, propisoclor, propoxicarbazona sódica, propizamida, prosulfocarb, prosulfuron, piraclonila, piraflufeno-etila, pirazolato, pirazosulfuron-etila, pirazoxifeno, piribenzoxim, piributicarb, piridafol, piridato, piriftalid, piriminobac-metila, piritiobac sódico, quinclorac, quinmerac, quinoclamina, quizalofop-etila, quizalofop-P- etila, quizalofop-P-tefurila, rimsulfuron, setoxidim, simazina, simetrina, S-metolaclor, sulcotriona, sulfentrazona, sulfometuron-metila, sulfosato, sulfosulfuron, tebutiuron, tepraloxidim, terbutilazina, terbutrina, tenilclor, tiazopir, tifensulfuron-metila, tiobencarb, tiocarbazila, tralcoxidim, triallate, triasulfuron, tribenuron-metila, triclopir, tridifano, trifloxisulfuron, trifluralin, triflusulfuron-metila, tritosulfuron, WL 110547, i.e., 5-fenóxi-1-[3-(trifluorometil)fenil]-1H- tetrazol; HOK-201, HOK-202, UBH-509; D-489; LS 82-556; KPP-300; NC-324; NC-330; KH-218; DPX-N8189; SC-0774; TH-547, DOWCO- 535; DK-8910; V-53482; PP-600; MBH-001; KIH-9201; ET-751; KIH- 6127; KIH-2023 e KIH5996.
[00115] Se o respectivo nome comum compreender uma pluralidade de formas do composto ativo, o nome de preferência define a forma comercialmente disponível.
[00116] Cada um dos demais compostos ativos mencionados (= compostos ativos (C*), (C1*), (C2*) etc.) podem ser então de preferência combinados com uma combinação binária de acordo com a presente invenção, segundo o esquema (A)+(B)+(C*) ou ainda segundo o esquema (A)+(B)+(C1*)+(C2*) etc.
[00117] As quantidades indicadas são taxas de aplicação (g i.a./ha = gramas de substância ativa por hectare) e, portanto, também definem as razões em uma co-formulação, uma pré-mistura, uma mistura de tanque ou uma aplicação sequencial dos compostos ativos combinados.
[00118] As combinações podem ser aplicadas tanto pelo método da pré-emergência como pelo método da pós-emergência. Isto se aplica tanto à pré-emergência como à pós-emergência de plantas daninhas e no controle seletivo de plantas daninhas na pré-emergência e na pós- emergência de plantas de lavoura. Formas mistas também são possíveis, por exemplo, depois da emergência das plantas de lavoura para controle das plantas daninhas em estágio pré- ou pós-emergente.
[00119] As combinações herbicidas de acordo com a invenção podem compreender componentes adicionais, por exemplo, outros compostos ativos contra organismos prejudiciais tal como plantas daninhas, animais que danificam as plantas ou fungosque danificam as plantas, aqui em particular compostos ativos do grupo dos herbicidas, fungicidas, inseticidas, acaricidas, nematicidas, miticidas e substâncias relacionadas.
[00120] Compostos fungicidamente ativos que podem ser usasdos em combinação com as composições herbicidas de acordo com a invenção são de preferência compostos ativos comerciais tradicionais, por exemplo, (de forma análoga aos herbicidas, os compostos geralmente estão indicados por seu nome comum, aqui na terminologia usual em inglês): 1) Inibidores (1.001) ciproconazole, (1.002) difenoconazole, (1.003) epoxiconazole, (1.004) fenhexamid, (1.005) fenpropidin, (1.006) fenpropimorf, (1.007) fenpirazamine, (1.008) fluquinconazole, (1.009) flutriafol, (1.010) imazalila, (1.011) imazalil sulfate, (1.012) ipconazole, (1.013) metconazole, (1.014) myclobutanila, (1.015) paclobutrazol, (1.016) procloraz, (1.017) propiconazole, (1.018) protioconazole, (1.019) pirisoxazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.022) tetraconazole, (1.023) triadimenol, (1.024) tridemorf, (1.025) triticonazole, (1.026) (1R,2S,5S)-5-(4-clorobenzil)-2- (clorometil)-2-metil -1-(1H-1,2,4-triazol-1-ilmetil)ciclopentanol, (1.027) (1S,2R,5R)-5-(4-clorobenzil)-2-(clorometil)-2-metil-1-(1H-1,2,4-triazol- 1-ilmetil)ciclopentanol, (1.028) (2R)-2-(1-clorociclopropil)-4-[(1R)-2,2- diclorociclopropil]-1-(1H-1,2,4-triazol-1-il)butan-2-ol, (1.029) (2R)-2-(1- clorociclopropil)-4-[(1S)-2,2-diclorociclopropil]-1-(1H-1,2,4-triazol-1- il)butan-2-ol, (1.030) (2R)-2-[4-(4-clorofenoxi)-2-(trifluorometil)fenil]-1- (1H-1,2,4-triazol-1-il) propan-2-ol, (1.031) (2S)-2-(1-clorociclopropil)-4- [(1R)-2,2-diclorociclopropil]-1-(1H-1,2,4-triazol-1-il)butan-2-ol, (1.032) (2S)-2-(1-clorociclopropil)-4-[(1S)-2,2-diclorociclopropil]-1-(1H-1,2,4- triazol-1-il)butan-2-ol, (1.033) (2S)-2-[4-(4-clorofenoxi)-2- (trifluorometil)fenil]-1-(1H-1,2,4-triazol-1-il)propan-2-ol, (1.034) (R)-[3- (4-cloro-2-fluorofenil)-5-(2,4-difluorofenil)-1,2-oxazol-4-il](piridin-3- il)metanol, (1.035) (S)-[3-(4-cloro-2-fluorofenil)-5-(2,4-difluorofenil)-1,2- oxazol-4-il](piridin-3-il)metanol, (1.036) [3-(4-cloro-2-fluorofenil)-5-(2,4- difluorofenil)-1,2-oxazol-4-il] (piridin-3-il)metanol, (1.037) 1-({(2R,4S)-2- [2-cloro-4-(4-clorofenoxi)fenil]-4-metil-1,3-dioxolan-2-il}metil)-1H-1,2,4- triazole, (1.038) 1-({(2S,4S)-2-[2-cloro-4-(4-clorofenoxi)fenil]-4-metil- 1,3-dioxolan-2-il}metil)-1H-1,2,4-triazole, (1.039) 1-{[3-(2-clorofenil)-2- (2,4-difluorofenil)oxiran-2-il]metil}-1H-1,2,4-triazol-5-il tiocianato, (1.040) 1-{[rel(2R,3R)-3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran-2- il]metil}-1H-1,2,4-triazol-5-il tiocianato, (1.041) 1-{[rel(2R,3S)-3-(2- clorofenil)-2-(2,4-difluorofenil)oxiran-2-il]metil}-1H-1,2,4-triazol-5-il tiocianato, (1.042) 2-[(2R,4R,5R)-1-(2,4-diclorofenil)-5-hidroxi-2,6,6- trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazole-3-tiona, (1.043) 2- [(2R,4R,5S)-1-(2,4-diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4- dihidro-3H-1,2,4-triazole-3-tiona, (1.044) 2-[(2R,4S,5R)-1-(2,4- diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4- triazole-3-tiona, (1.045) 2-[(2R,4S,5S)-1-(2,4-diclorofenil)-5-hidroxi- 2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazole-3-tiona, (1.046) 2- [(2S,4R,5R)-1-(2,4-diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4- dihidro-3H-1,2,4-triazole-3-tiona, (1.047) 2-[(2S,4R,5S)-1-(2,4- diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4- triazole-3-tiona, (1.048) 2-[(2S,4S,5R)-1-(2,4-diclorofenil)-5-hidroxi- 2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazole-3-tiona, (1.049) 2- [(2S,4S,5S)-1-(2,4-diclorofenil)-5-hidroxi-2,6,6-trimetilheptan-4-il]-2,4- dihidro-3H-1,2,4-triazole-3-tiona, (1.050) 2-[1-(2,4-diclorofenil)-5- hidroxi-2,6,6-trimetilheptan-4-il]-2,4-dihidro-3H-1,2,4-triazole-3-tiona, (1.051) 2-[2-cloro-4-(2,4-dichlorofenoxi)fenil]-1-(1H-1,2,4-triazol-1- il)propan-2-ol, (1.052) 2-[2-cloro-4-(4-clorofenoxi)fenil]-1-(1H-1,2,4- triazol-1-il)butan-2-ol, (1.053) 2-[4-(4-clorofenoxi)-2-(trifluorometil)fenil]- 1-(1H-1,2,4-triazol-1-il)butan-2-ol, (1.054) 2-[4-(4-clorofenoxi)-2- (trifluorometil)fenil]-1-(1H-1,2,4-triazol-1-il)pentan-2-ol, (1.055) 2-[4-(4- clorofenoxi)-2-(trifluorometil)fenil]-1-(1H-1,2,4-triazol-1-il)propan-2-ol, (1.056) 2-{[3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran-2-il]metil}-2,4- dihidro-3H-1,2,4-triazole-3-tiona, (1.057) 2-{[rel(2R,3R)-3-(2-clorofenil)- 2-(2,4-difluorofenil)oxiran-2-il]metil}-2,4-dihidro-3H-1,2,4-triazole-3- tiona, (1.058) 2-{[rel(2R,3S)-3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran- 2-il]metil}-2,4-dihidro-3H-1,2,4-triazole-3-tiona, (1.059) 5-(4- clorobenzil)-2-(clorometil)-2-metil-1-(1H-1,2,4-triazol-1- ilmetil)ciclopentanol, (1.060) 5-(allilsulfanil)-1-{[3-(2-clorofenil)-2-(2,4- difluorofenil)oxiran-2-il]metil}-1H-1,2,4-triazole, (1.061) 5-(allilsulfanil)- 1-{[rel(2R,3R)-3-(2-clorofenil)-2-(2,4-difluorofenil)oxiran-2-il]metil}-1H- 1,2,4-triazole, (1.062) 5-(allilsulfanil)-1-{[rel(2R,3S)-3-(2-clorofenil)-2- (2,4-difluorofenil)oxiran-2-il]metil}-1H-1,2,4-triazole, (1.063) N'-(2,5- dimetil-4-{[3-(1,1,2,2-tetrafluoroetoxi)fenil]sulfanil}fenil)-N-etil-N- metilimidoformamida, (1.064) N'-(2,5-dimetil-4-{[3-(2,2,2- trifluoroetoxi)fenil]sulfanil}fenil)-N-etil-N-metilimidoformamida, (1.065) N'-(2,5-dimetil-4-{[3-(2,2,3,3-tetrafluoropropoxi)fenil]sulfanil}fenil)-N-etil- N-metilimidoformamida, (1.066) N'-(2,5-dimetil-4-{[3- (pentafluoroetoxi)fenil]sulfanil}fenil)-N-etil-N-metilimidoformamida, (1.067) N'-(2,5-dimetil-4-{3-[(1,1,2,2-tetrafluoroetil)sulfanil]fenoxi}fenil)- N-etil-N-metilimidoformamida, (1.068) N'-(2,5-dimetil-4-{3-[(2,2,2- trifluoroetil)sulfanil]fenoxi}fenil)-N-etil-N-metilimidoformamida, (1.069) N'-(2,5-dimetil-4-{3-[(2,2,3,3-tetrafluoropropil)sulfanil]fenoxi}fenil)-N-etil- N-metilimidoformamida, (1.070) N'-(2,5-dimetil-4-{3- [(pentafluoroetil)sulfanil]fenoxi}fenil)-N-etil-N-metilimidoformamida, (1.071) N'-(2,5-dimetil-4-fenoxifenil)-N-etil-N-metilimidoformamida, (1.072) N'-(4-{[3-(difluorometoxi)fenil]sulfanil}-2,5-dimetilfenil)-N-etil-N- metilimidoformamida, (1.073) N'-(4-{3-[(difluorometil)sulfanil]fenoxi}- 2,5-dimetilfenil)-N-etil-N-metilimidoformamida, (1.074) N'-[5-bromo-6- (2,3-dihidro-1H-inden-2-iloxi)-2-metilpiridin-3-il]-N-etil-N- metilimidoformamida, (1.075) N'-{4-[(4,5-dicloro-1,3-tiazol-2-il)oxi]-2,5- dimetilfenil}-N-etil-N-metilimidoformamida, (1.076) N'-{5-bromo-6-[(1R)- 1-(3,5-difluorofenil)etoxi]-2-metilpiridin-3-il}-N-etil-N- metilimidoformamida, (1.077) N'-{5-bromo-6-[(1S)-1-(3,5- difluorofenil)etoxi]-2-metilpiridin-3-il}-N-etil-N-metilimidoformamida, (1.078) N'-{5-bromo-6-[(cis-4-isopropilciclohexil)oxi]-2-metilpiridin-3-il}- N-etil-N-metilimidoformamida, (1.079) N'-{5-bromo-6-[(trans-4- isopropilciclohexil)oxi]-2-metilpiridin-3-il}-N-etil-N-metilimidoformamida, (1.080) N'-{5-bromo-6-[1-(3,5-difluorofenil)etoxi]-2-metilpiridin-3-il}-N- etil-N-metilimidoformamida, (1.081) mefentrifluconazole, (1.082) ipfentrifluconazole. 2) Inibidores da cadeia respiratória no complexo I ou II, por exemplo, (2.001) benzovindiflupir, (2.002) bixafen, (2.003) boscalid, (2.004) carboxin, (2.005) fluopiram, (2.006) flutolanila, (2.007) fluxapiroxad, (2.008) furametpir, (2.009) isofetamid, (2.010) isopirazam (enantiômero anti-epimérico 1R,4S,9S), (2.011) isopirazam (enantiômero anti-epimérico 1S,4R,9R), (2.012) isopirazam (racemato anti-epimérico 1RS,4SR,9SR), (2.013) isopirazam (mistura do racemato syn-epimérico 1RS,4SR,9RS e do racemato anti-epimérico 1RS,4SR,9SR), (2.014) isopirazam (enantiômero syn-epimérico 1R,4S,9R), (2.015) isopirazam (enantiômero syn-epimérico 1S,4R,9S), (2.016) isopirazam (racemato syn-epimérico 1RS,4SR,9RS), (2.017) penflufen, (2.018) pentiopirad, (2.019) pidiflumetofen, (2.020) piraziflumid, (2.021) sedaxane, (2.022) 1,3-dimetil-N-(1,1,3-trimetil-2,3- dihidro-1H-inden-4-il)-1H-pirazole-4-carboxamida, (2.023) 1,3-dimetil- N-[(3R)-1,1,3-trimetil-2,3-dihidro-1H-inden-4-il]-1H-pirazole-4- carboxamida, (2.024) 1,3-dimetil-N-[(3S)-1,1,3-trimetil-2,3-dihidro-1H- inden-4-il]-1H-pirazole-4-carboxamida, (2.025) 1-metil-3-(trifluorometil)- N-[2'-(trifluorometil)bifenil-2-il]-1H-pirazole-4-carboxamida, (2.026) 2- fluoro-6-(trifluorometil)-N-(1,1,3-trimetil-2,3-dihidro-1H-inden-4- il)benzamida, (2.027) 3-(difluorometil)-1-metil-N-(1,1,3-trimetil-2,3- dihidro-1H-inden-4-il)-1H-pirazole-4-carboxamida, (2.028) 3- (difluorometil)-1-metil-N-[(3R)-1,1,3-trimetil-2,3-dihidro-1H-inden-4-il]- 1H-pirazole-4-carboxamida, (2.029) 3-(difluorometil)-1-metil-N-[(3S)- 1,1,3-trimetil-2,3-dihidro-1H-inden-4-il]-1H-pirazole-4-carboxamida, (2.030) 3-(difluorometil)-N-(7-fluoro-1,1,3-trimetil-2,3-dihidro-1H-inden- 4-il)-1-metil-1H-pirazole-4-carboxamida, (2.031) 3-(difluorometil)-N- [(3R)-7-fluoro-1,1,3-trimetil-2,3-dihidro-1H-inden-4-il]-1-metil-1H- pirazole-4-carboxamida, (2.032) 3-(difluorometil)-N-[(3S)-7-fluoro-1,1,3- trimetil-2,3-dihidro-1H-inden-4-il]-1-metil-1H-pirazole-4-carboxamida, (2.033) 5,8-difluoro-N-[2-(2-fluoro-4-{[4-(trifluorometil)piridin-2- il]oxi}fenil)etil]quinazolin-4-amine, (2.034) N-(2-ciclopentil-5-fluoroben- zil)-N-ciclopropil-3-(difluorometil)-5-fluoro-1-metil-1H-pirazole-4- carboxamida, (2.035) N-(2-tert-butil-5-metilbenzil)-N-ciclopropil-3- (difluorometil)-5-fluoro-1-metil-1H-pirazole-4-carboxamida, (2.036) N- (2-tert-butilbenzil)-N-ciclopropil-3-(difluorometil)-5-fluoro-1-metil-1H- pirazole-4-carboxamida, (2.037) N-(5-cloro-2-etilbenzil)-N-ciclopropil-3- (difluorometil)-5-fluoro-1-metil-1H-pirazole-4-carboxamida, (2.038) N- (5-cloro-2-isopropilbenzil)-N-ciclopropil-3-(difluorometil)-5-fluoro-1- metil-1H-pirazole-4-carboxamida, (2.039) N-[(1R,4S)-9- (diclorometilene)-1,2,3,4-tetrahidro-1,4-metanonaftalen-5-il]-3- (difluorometil)-1-metil-1H-pirazole-4-carboxamida, (2.040) N-[(1S,4R)- 9-(diclorometilene)-1,2,3,4-tetrahidro-1,4-metanonaftalen-5-il]-3- (difluorometil)-1-metil-1H-pirazole-4-carboxamida, (2.041) N-[1-(2,4- diclorofenil)-1-metoxipropan-2-il]-3-(difluorometil)-1-metil-1H-pirazole- 4-carboxamida, (2.042) N-[2-cloro-6-(trifluorometil)benzil]-N-ciclopropil- 3-(difluorometil)-5-fluoro-1-metil-1H-pirazole-4-carboxamida, (2.043) N- [3-cloro-2-fluoro-6-(trifluorometil)benzil]-N-ciclopropil-3-(difluorometil)-5- fluoro-1-metil-1H-pirazole-4-carboxamida, (2.044) N-[5-cloro-2- (trifluorometil)benzil]-N-ciclopropil-3-(difluorometil)-5-fluoro-1-metil-1H- pirazole-4-carboxamida, (2.045) N-ciclopropil-3-(difluorometil)-5-fluoro- 1-metil-N-[5-metil-2-(trifluorometil)benzil]-1H-pirazole-4-carboxamida, (2.046) N-ciclopropil-3-(difluorometil)-5-fluoro-N-(2-fluoro-6- isopropilbenzil)-1-metil-1H-pirazole-4-carboxamida, (2.047) N- ciclopropil-3-(difluorometil)-5-fluoro-N-(2-isopropil-5-metilbenzil)-1- metil-1H-pirazole-4-carboxamida, (2.048) N-ciclopropil-3- (difluorometil)-5-fluoro-N-(2-isopropilbenzil)-1-metil-1H-pirazole-4- carbotioamida, (2.049) N-ciclopropil-3-(difluorometil)-5-fluoro-N-(2- isopropilbenzil)-1-metil-1H-pirazole-4-carboxamida, (2.050) N- ciclopropil-3-(difluorometil)-5-fluoro-N-(5-fluoro-2-isopropilbenzil)-1- metil-1H-pirazole-4-carboxamida, (2.051) N-ciclopropil-3- (difluorometil)-N-(2-etil-4,5-dimetilbenzil)-5-fluoro-1-metil-1H-pirazole-4- carboxamida, (2.052) N-ciclopropil-3-(difluorometil)-N-(2-etil-5- fluorobenzil)-5-fluoro-1-metil-1H-pirazole-4-carboxamida, (2.053) N- ciclopropil-3-(difluorometil)-N-(2-etil-5-metilbenzil)-5-fluoro-1-metil-1H- pirazole-4-carboxamida, (2.054) N-ciclopropil-N-(2-ciclopropil-5- fluorobenzil)-3-(difluorometil)-5-fluoro-1-metil-1H-pirazole-4- carboxamida, (2.055) N-ciclopropil-N-(2-ciclopropil-5-metilbenzil)-3- (difluorometil)-5-fluoro-1-metil-1H-pirazole-4-carboxamida, (2.056) N- ciclopropil-N-(2-ciclopropilbenzil)-3-(difluorometil)-5-fluoro-1-metil-1H- pirazole-4-carboxamida.. 3) Inibidores da cadeia respiratória que agem no complexo III, por exemplo, (3.001) ametoctradin, (3.002) amisulbrom, (3.003) azoxistrobin, (3.004) coumetoxistrobin, (3.005) coumoxistrobin, (3.006) ciazofamid, (3.007) dimoxistrobin, (3.008) enoxastrobin, (3.009) famoxadon, (3.010) fenamidon, (3.011) flufenoxistrobin, (3.012) fluoxastrobin, (3.013) kresoxim-metil, (3.014) metominostrobin, (3.015) orysastrobin, (3.016) picoxistrobin, (3.017) piraclostrobin, (3.018) pirametostrobin, (3.019) piraoxistrobin, (3.020) trifloxistrobin, (3.021) (2E)-2-{2-[({[(1E)-1-(3-{[(E)-1-fluoro-2- fenilvinil]oxi}fenil)etilidene]amino}oxi)metil]fenil}-2-(metoxiimino)-N- metilacetamida, (3.022) (2E,3Z)-5-{[1-(4-clorofenil)-1H-pirazol-3-il]oxi}- 2-(metoxiimino)-N,3-dimetilpent-3-enamida, (3.023) (2R)-2-{2-[(2,5- dimetilfenoxi)metil]fenil}-2-metoxi-N-metilacetamida, (3.024) (2S)-2-{2- [(2,5-dimetilfenoxi)metil]fenil}-2-metoxi-N-metilacetamida, (3.025) (3S,6S,7R,8R)-8-benzil-3-[({3-[(isobutyriloxi)metoxi]-4-metoxipiridin-2- il}carbonil)amino]-6-metil-4,9-dioxo-1,5-dioxonan-7-il 2- metilpropanoate, (3.026) 2-{2-[(2,5-dimetilfenoxi)metil]fenil}-2-metoxi- N-metilacetamida, (3.027) formamido-2-hidroxibenzamida, fluorofenil)-1H-pirazol-3-il]oxi}-2-(metoxiimino)-N,3-dimetilpent-3- enamida, (3.029) metil {5-[3-(2,4-dimetilfenil)-1H-pirazol-1-il]-2- metilbenzil}carbamate. 4) Inibidores da mitose e da divisão celular, por exemplo, (4.001) carbendazim, (4.002) dietofencarb, (4.003) etaboxam, (4.004) fluopicolid, (4.005) pencicuron, (4.006) tiabendazole, (4.007) tiofanato- metil, (4.008) zoxamida, fenilpiridazine, (4.010) metilpiridazine, (4.011) trifluorofenil)piridazine, difluorofenil)-1,3-dimetil-1H-pirazol-5-amine, fluorofenil)-N-(2-bromo-6-fluorofenil)-1,3-dimetil-1H-pirazol-5-amine, (4.014) 4-(2-bromo-4-fluorofenil)-N-(2-bromofenil)-1,3-dimetil-1H- pirazol-5-amine, (4.015) 4-(2-bromo-4-fluorofenil)-N-(2-cloro-6- fluorofenil)-1,3-dimetil-1H-pirazol-5-amine, (4.016) 4-(2-bromo-4- fluorofenil)-N-(2-clorofenil)-1,3-dimetil-1H-pirazol-5-amine, (4.017) 4-(2- bromo-4-fluorofenil)-N-(2-fluorofenil)-1,3-dimetil-1H-pirazol-5-amine, (4.018) 4-(2-cloro-4-fluorofenil)-N-(2,6-difluorofenil)-1,3-dimetil-1H- pirazol-5-amine, (4.019) 4-(2-cloro-4-fluorofenil)-N-(2-cloro-6- fluorofenil)-1,3-dimetil-1H-pirazol-5-amine, (4.020) 4-(2-cloro-4- fluorofenil)-N-(2-clorofenil)-1,3-dimetil-1H-pirazol-5-amine, (4.021) 4-(2- cloro-4-fluorofenil)-N-(2-fluorofenil)-1,3-dimetil-1H-pirazol-5-amine, (4.022) 4-(4-clorofenil)-5-(2,6-difluorofenil)-3,6-dimetilpiridazine, (4.023) N-(2-bromo-6-fluorofenil)-4-(2-cloro-4-fluorofenil)-1,3-dimetil-1H- pirazol-5-amine, (4.024) N-(2-bromofenil)-4-(2-cloro-4-fluorofenil)-1,3- dimetil-1H-pirazol-5-amine, (4.025) N-(4-cloro-2,6-difluorofenil)-4-(2- cloro-4-fluorofenil)-1,3-dimetil-1H-pirazol-5-amine. 5) Compostos com atividade em múltiplos sítios, por exemplo, (5.001) Bordeaux mixture, (5.002) captafol, (5.003) captan, (5.004) clortalonila, (5.005) copper hidroxide, (5.006) copper naftenato, (5.007) copper oxide, (5.008) copper oxicloride, (5.009) copper(2+) sulfate, (5.010) ditianon, (5.011) dodine, (5.012) folpet, (5.013) mancozeb, (5.014) maneb, (5.015) metiram, (5.016) zinc metiram, (5.017) copper oxine, (5.018) propineb, (5.019) sulfur and sulfur preparations including calcium polysulfide, (5.020) tiram, (5.021) zineb, (5.022) ziram, (5.023) 6-etil-5,7-dioxo-6,7-dihidro-5H- pirrolo[3',4':5,6][1,4]ditiino[2,3-c][1,2]tiazole-3-carbonitrile. 6) Compostos capazes de desencadear a defesa do hospedeiro, por exemplo, (6.001) acibenzolar-S-metil, (6.002) isotianila, (6.003) probenazole, (6.004) tiadinila. 7) Inibidores da biossíntese de aminoácidos e/ou proteínas, por exemplo, (7.001) ciprodinila, (7.002) kasugamicina, (7.003) kasugamicina hidrocloride hidrate, (7.004) oxitetracicline, (7.005) pirimetanila, (7.006) 3-(5-fluoro-3,3,4,4-tetrametil-3,4- dihidroisoquinolin-1-il)quinoline. 8) Inibidores da produção de ATP, por exemplo, (8.001) siltiofam. 9) Inibidores da síntese da parede celular, por exemplo, (9.001) bentiavalicarb, (9.002) dimetomorf, (9.003) flumorf, (9.004) iprovalicarb, (9.005) mandipropamid, (9.006) pirimorf, (9.007) valifenalate, (9.008) (2E)-3-(4-tert-butilfenil)-3-(2-cloropiridin-4-il)-1- (morfolin-4-il)prop-2-en-1-ona, (9.009) (2Z)-3-(4-tert-butilfenil)-3-(2- cloropiridin-4-il)-1-(morfolin-4-il)prop-2-en-1-ona. 10) Inibidores da síntese de lipídios e membranas, por exemplo, (10.001) propamocarb, (10.002) propamocarb hidrocloride, (10.003) tolclofos-metil. 11) Inibidores da biossíntese de melanina, por exemplo, (11.001) triciclazole, (11.002) 2,2,2-trifluoroetil-{3-metil-1-[(4- metilbenzoil)amino]butan-2-il}carbamate. 12) Inibidores da síntese de ácidos nucleicos, por exemplo, (12.001) benalaxil, (12.002) benalaxil-M (kiralaxil), (12.003) metalaxil, (12.004) metalaxil-M (mefenoxam). 13) Inibidores da transdução de sinais, por exemplo, (13.001) fludioxonila, (13.002) iprodiona, (13.003) procimidona, (13.004) proquinazid, (13.005) quinoxifen, (13.006) vinclozolin. 14) Compostos que atuam como desacopladores, por exemplo, (14.001) fluazinem, (14.002) meptildinocap. 15) Outros compostos, por exemplo, (15.001) ácido abscísico, (15.002) bentiazole, (15.003) betoxazin, (15.004) capsimicina, (15.005) carvona, (15.006) cinometionat, (15.007) cufraneb, (15.008) ciflufenamid, (15.009) cimoxanila, (15.010) ciprosulfamida, (15.011) flutianila, (15.012) fosetil-alumínio, (15.013) fosetil-cácio, (15.014) fosetil-sódico, (15.015) metil isotiocianato, (15.016) metrafenon, (15.017) mildiomicina, (15.018) natamicina, (15.019) nickel dimetilditiocarbamate, (15.020) nitrotal-isopropil, (15.021) oxamocarb, (15.022) oxatiapiprolin, (15.023) oxifentiin, (15.024) pentaclorofenol and salts, (15.025) ácido fosfônico e seus sais, (15.026) propamocarb-fosetilato, (15.027) piriofenona (clazafenona), (15.028) tebufloquin, (15.029) tecloftalam, (15.030) tolnifanide, (15.031) 1-(4-{4-[(5R)-5-(2,6-difluorofenil)-4,5-dihidro-1,2- oxazol-3-il]-1,3-tiazol-2-il}piperidin-1-il)-2-[5-metil-3-(trifluorometil)-1H- pirazol-1-il]etanona, (15.032) 1-(4-{4-[(5S)-5-(2,6-difluorofenil)-4,5- dihidro-1,2-oxazol-3-il]-1,3-tiazol-2-il}piperidin-1-il)-2-[5-metil-3- (trifluorometil)-1H-pirazol-1-il]etanona, (15.033) 2-(6-benzilpiridin-2- il)quinazoline, (15.034) 2,6-dimetil-1H,5H-[1,4]ditiino[2,3-c:5,6- c']dipirrole-1,3,5,7(2H,6H)-tetrona, (15.035) 2-[3,5-bis(difluorometil)-1H- pirazol-1-il]-1-[4-(4-{5-[2-(prop-2-yn-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol- 3-il}-1,3-tiazol-2-il)piperidin-1-il]etanona, (15.036) 2-[3,5- bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{5-[2-cloro-6-(prop-2-yn-1- iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3-tiazol-2-il)piperidin-1- il]etanona, (15.037) 2-[3,5-bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{5- [2-fluoro-6-(prop-2-yn-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3- tiazol-2-il)piperidin-1-il]etanona, (15.038) 2-[6-(3-fluoro-4-metoxifenil)-5- metilpiridin-2-il]quinazoline, (15.039) 2-{(5R)-3-[2-(1-{[3,5- bis(difluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-1,3-tiazol-4-il]-4,5- dihidro-1,2-oxazol-5-il}-3-clorofenil metanesulfonato, (15.040) 2-{(5S)- 3-[2-(1-{[3,5-bis(difluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-1,3- tiazol-4-il]-4,5-dihidro-1,2-oxazol-5-il}-3-clorofenil metanesulfonato, (15.041) 2-{2-[(7,8-difluoro-2-metilquinolin-3-il)oxi]-6-fluorofenil}propan- 2-ol, (15.042) 2-{2-fluoro-6-[(8-fluoro-2-metilquinolin-3- il)oxi]fenil}propan-2-ol, (15.043) 2-{3-[2-(1-{[3,5-bis(difluorometil)-1H- pirazol-1-il]acetil}piperidin-4-il)-1,3-tiazol-4-il]-4,5-dihidro-1,2-oxazol-5- il}-3-clorofenil metanesulfonato, (15.044) 2-{3-[2-(1-{[3,5- bis(difluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-1,3-tiazol-4-il]-4,5- dihidro-1,2-oxazol-5-il}fenil metanesulfonato, (15.045) 2-fenilfenol and salts tereof, (15.046) 3-(4,4,5-trifluoro-3,3-dimetil-3,4- dihidroisoquinolin-1-il)quinoline, (15.047) 3-(4,4-difluoro-3,3-dimetil-3,4- dihidroisoquinolin-1-il)quinoline, (15.048) 4-amino-5-fluoropirimidin-2-ol (tautomeric form: 4-amino-5-fluoropirimidin-2(1H)-ona), (15.049) ácido 4-oxo-4-[(2-feniletil)amino]butirico, (15.050) 5-amino-1,3,4-tiadiazole-2- tiol, (15.051) 5-cloro-N'-fenil-N'-(prop-2-yn-1-il)tiofene-2- sulfonohidrazide, (15.052) 5-fluoro-2-[(4-fluorobenzil)oxi]pirimidin-4- amina, (15.053) 5-fluoro-2-[(4-metilbenzil)oxi]pirimidin-4-amine, (15.054) 9-fluoro-2,2-dimetil-5-(quinolin-3-il)-2,3-dihidro-1,4- benzoxazepine, (15.055) but-3-yn-1-il {6-[({[(Z)-(1-metil-1H-tetrazol-5- il)(fenil)metilene]amino}oxi)metil]piridin-2-il}carbamato, (15.056) etil (2Z)-3-amino-2-ciano-3-fenilacrilate, (15.057) ácido fenazine-1- carboxilico, (15.058) propil 3,4,5-trihidroxibenzoato, (15.059) quinolin- 8-ol, (15.060) quinolin-8-ol sulfato (2:1), (15.061) tert-butil {6-[({[(1- metil-1H-tetrazol-5-il)(fenil)metilene]amino}oxi)metil]piridin-2- il}carbamate, (15.062) 5-fluoro-4-imino-3-metil-1-[(4-metilfenil)sulfonil]- 3,4-dihidropirimidin-2(1H)-ona. Fungicidas preferidos são selecionados do grupo que consiste em benalaxil, bitertanol, bromuconazole, captafol, carbendazim, carpropamid, ciazofamid, ciproconazole, dietofencarb, edifenfos, fenpropimorf, fentine, fluquinconazol, fosetil, fluoroimida, folpet, iminoctadine, iprodionem, iprovalicarb, kasugamicina, maneb, nabam, pencicuron, procloraz, propamocarb, propineb, pirimetanila, sprioxamina, quintozene, tebuconazole, tolilfluanid, triadimefon, triadimenol, trifloxistrobin, zineb. Compostos ativos inseticidas, acaricidas, nematicidas, miticidas e compostos ativos relacionados são, por exemplo, (de forma análoga aos herbicidas e fungicidas, os compostos estão indicados por seu nome comum, se possível, aqui na terminologia usual em inglês): (1) Inibidores da acetilcolinesterase (AChE), de preferência carbamatos selecionados dentre alanycarb, aldicarb, bendiocarb, benfuracarb, butocarboxim, butoxicarboxim, carbarila, carbofuran, carbosulfan, etiofencarb, fenobucarb, formetanato, furatiocarb, isoprocarb, metiocarb, metomil, metolcarb, oxamil, pirimicarb, propoxur, tiodicarb, tiofanox, triazamate, trimetacarb, XMC e xililcarb; ou organofosfatos selecionados dentre acefate, azametifos, azinfos- etil, azinfos-metil, cadusafos, cloretoxifos, clorfenvinfos, clormefos, clorpirifos-metil, coumafos, cianofos, demeton-S-metil, diazinon, diclorvos/DDVP, dicrotofos, dimetoate, dimetilvinfos, disulfoton, EPN, etion, etoprofos, famfur, fenamifos, fenitrotion, fention, fostiazate, heptenofos, imiciafos, isofenfos, isopropil-O-(metoxiaminotiofosforil) salicilate, isoxation, malation, mecarbam, metamidofos, metidation, mevinfos, monocrotofos, naled, ometoate, oxidemeton-metil, paration- metil, fentoate, forate, fosalona, fosmet, fosfamidon, foxim, pirimifos- metil, profenofos, propetamfos, protiofos, piraclofos, piridafention, quinalfos, sulfotep, tebupirimfos, temefos, terbufos, tetraclorvinfos, tiometon, triazofos, triclorfon e vamidotion.. (2) Bloqueadores do canal de cloreto com acesso para GABA, de preferência ciclodiene-organoclorines selecionado dentre clordane e endosulfan, ou fenilpirazoles (fiproles) selecionado dentre etiprole e fipronila. (3) Moduladores do canal de sódio, de preferência piretroides selecionados dentre acrinatrin, alletrin, d-cis-trans alletrin, d-trans alletrin, bifentrin, bioalletrin, bioalletrin S-ciclopentenil isomer, bioresmetrin, cicloprotrin, ciflutrin, beta-ciflutrin, cihalotrin, lambda- cihalotrin, gamma-cihalotrin, cipermetrin, alfa-cipermetrin, beta- cipermetrin, teta-cipermetrin, zeta-cipermetrin, cifenotrin [(1R)-trans isomer], deltametrin, empentrin [isômero (EZ)-(1R)], esfenvalerate, etofenprox, fenpropatrin, fenvalerate, flucitrinato, flumetrin, tau- fluvalinato, halfenprox, imiprotrin, kadetrin, momfluorotrin, permetrin, fenotrin [isômero (1R)-trans], pralletrin, piretrinas (piretrum), resmetrin, silafluofen, teflutrin, tetrametrin, tetrametrin [isômero (1R)], tralometrin e transflutrin ou DDT ou metoxiclor. (4) Moduladores competitivos do receptor da acetilcolina nicotínica (nAChR), de preferência neonicotinoides selecionados dentre acetamiprid, clotianidin, dinotefuran, imidacloprid, nitenpiram, tiacloprid e tiametoxam, ou nicotine, ou sulfoximinas selecionadas dentre sulfoxaflor, ou butenolidas selecionadas dentre flupiradifurona. (5) Moduladores alostéricos do receptor da acetilcolina nicotínica (nAChR), de preferência espinosinas selecionadas dentre spinetoram e spinosad. (6) Moduladores alostéricos do canal de cloreto com acesso para glutamato (GluCl), de preferência avermectins/milbemicinas selecionadas dentre abamectin, emamectin benzoate, lepimectin e milbemectin. (7) Miméticos do hormônio juvenila, de preferência análogos do hormônio juvenil selecionados dentre hidroprene, kinoprene e metoprene, ou fenoxicarb ou piriproxifen. (8) Inibidores inespecíficos (múltiplos sítios) diversos, de preferência halogenetos de alquila selecionados dentre metil bromida e outros halogenetos de alquila; ou cloropicrin ou sulfuril fluoride ou borax ou geradores de tártaro emético ou isocianato de metila selecionados dentre diazomet e metam. (9) Moduladores do canal de TRPV dos órgãos cordotonais selecionados dentre pimetrozine e pirifluquinazon. (10) Inibidores do crescimento de ácaros selecionados dentre clofentezine, hexytiazox, diflovidazin e etoxazole. (11) disruptores microbianos de membranas do intestino médio dos insetos selecionados dentre Bacillus thuringiensis subespécie israelensis, Bacillus sphaericus, Bacillus thuringiensis subespécie aizawai, Bacillus thuringiensis sub-espécie kurstaki, Bacillus thuringiensis sub-espécie tenebrionis, e proteínas vegetais de B.t. selecionadas dentre Cry1Ab, Cry1Ac, Cry1Fa, Cry1A.105, Cry2Ab, VIP3A, mCry3A, Cry3Ab, Cry3Bb e Cry34Ab1/35Ab1. (12) Inibidores da ATP sintase mitocondrial, de preferência disruptores de ATP selecionados dentre diafentiuron, ou compostos de organoestanho selecionados dentre azociclotin, cihexatin e fenbutatin oxide, ou propargite ou tetradifon. (13) Desacopladores da fosforilação oxidativa via rompimento do gradiente protônico selecionados dentre clorfenapir, DNOC e sulfluramid. (14) Bloqueadores do canal do receptor da acetilcolina nicotínica selecionados dentre bensultap, cartap hidrocloride, tiociclam, e tiosultap-sódico. (15) Inibidores da biossíntese da quitina, tipo 0, selecionados dentre bistrifluron, clorfluazuron, diflubenzuron, flucicloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron e triflumuron. (16) Inibidores da biossíntese da quitina, tipo 1, selecionados dentre buprofezin. (17) Disruptores de mudas (especialmente no caso de dípteros) selecionados dentre ciromazine. (18) Agonistas do receptor da ecdisona selecionados dentre cromafenozide, halofenozide, metoxifenozide e tebufenozide. (19) Agonistas do receptor da octopamina selecionados dentre amitraz. (20) Inibidores do transporte de elétrons do complexo mitocondrial III selecionados dentre hidrametilnon, acequinocil e fluacrypirim. (21) Inibidores do transporte de elétrons do complexo mitocondrial I, de preferência acaricidas METI selecionados dentre fenazaquin, fenpiroximate, pirimidifen, piridaben, tebufenpirad e tolfenpirad, ou rotenona (Derris). (22) Bloqueadores do canal de sódio dependente da voltagem selecionados dentre indoxacarb e metaflumizona. (23) Inibidores da acetil-CoA carboxilase, de preferência derivados de ácido tetrônico e tetrâmico selecionados dentre spirodiclofen, spiromesifen e spirotetramat. (24) Inibidores do transporte de elétrons do complexo mitocondrial IV, de preferência fosfinas selecionadas dentre fosfeto de alumínio, fosfeto de cálcio, fosfina e fosfeto de zinco, ou cianetos selecionados dentre cianeto de cálcio, cianeto de potássio e cianeto de sódio. (25) Inibidores do transporte de elétrons do complexo mitocondrial II, de preferência derivados de beta-ceto nitrila selecionados dentre cienopirafen e ciflumetofen, ou carboxanilidas selecionadas dentre piflubumida. (28) Moduladores do receptor de rianodina, de preferência diamidas selecionadas dentre clorantraniliprole, ciantraniliprole e flubendiamida. (29) Moduladores dos órgãos cordotonais (com estrutura alvo indefinida) selecionados dentre flonicamid. (30) Outros compostos ativos selecionados dentre acinonapir, afidopiropen, afoxolaner, azadiractin, benclotiaz, benzoximate, benzpirimoxan, bifenazate, broflanilide, bromopropilate, cinometionat, cloropralletrin, cryolite, ciclaniliprole, cicloxaprid, cihalodiamida, dicloromezotiaz, dicofol, epsilon metoflutrin, epsilon momflutrin, flometoquin, fluazaindolizine, fluensulfona, flufenerim, flufenoxistrobin, flufiprole, fluhexafon, fluopiram, flupirimin, fluralaner, fluxametamida, fufenozide, guadipir, heptaflutrin, imidaclotiz, iprodiona, kappa bifentrin, kappa teflutrin, lotilaner, meperflutrin, oxazosulfil, paicongding, piridalil, pirifluquinazon, piriminostrobin, spirobudiclofen, spiropidion, tetrametilflutrin, tetraniliprole, tetraclorantraniliprole, tigolaner, tioxazafen, tiofluoximate, triflumezopirim e iodometane; adicionalmente preparações à base de Bacillus firmus (I-1582, BioNeem, Votivo), e os seguintes compostos: 1-{2-fluoro-4-metil-5- [(2,2,2-trifluoroetil)sulfinil]fenil}-3-(trifluorometil)-1H-1,2,4-triazole-5- amine (conhecido através do documento WO2006/043635) (CAS 885026-50-6), {1'-[(2E)-3-(4-clorofenil)prop-2-en-1-il]-5- fluorospiro[indole-3,4'-piperidine]-1(2H)-il}(2-cloropiridin-4-il)metanona (conhecido através do documento WO2003/106457) (CAS 637360-237), 2-cloro-N-[2-{1-[(2E)-3-(4-clorofenil)prop-2-en-1-il]piperidin-4-il}-4- (trifluorometil)fenil]isonicotinamida (conhecido através do documento WO2006/003494) (CAS 872999-66-1), 3-(4-cloro-2,6-dimetilfenil)-4- hidroxi-8-metoxi-1,8-diazaspiro[4.5]dec-3-en-2-ona (conhecido através do documento WO 2010052161) (CAS 1225292-17-0), 3-(4-cloro-2,6- dimetilfenil)-8-metoxi-2-oxo-1,8-diazaspiro[4.5] dec-3-en-4-il etilcarbonato (conhecido através do documento EP 2647626) (CAS- 1440516-42-6), 4-(but-2-yn-1-iloxi)-6-(3,5-dimetilpiperidin-1-il)-5- fluoropirimidine (conhecido através do documento WO2004/099160) (CAS 792914-58-0), PF1364 (conhecido através do documento JP2010/018586) (CAS Reg.No. 1204776-60-2), (3E)-3-[1-[(6-cloro-3- piridil)metil]-2-piridilidene]-1,1,1-trifluoropropan-2-ona (conhecido através do documento WO2013/144213) (CAS 1461743-15-6), N-[3- (benzilcarbamoil)-4-clorofenil]-1-metil-3-(pentafluoroetil)-4- (trifluorometil)-1H-pirazole-5-carboxamida (conhecido através do documento WO2010/051926) (CAS 1226889-14-0), 5-bromo-4-cloro- N-[4-cloro-2-metil-6-(metilcarbamoil)fenil]-2-(3-cloro-2-piridil)pirazole-3- carboxamida (conhecido através do documento CN103232431) (CAS 1449220-44-3), 4-[5-(3,5-diclorofenil)-4,5-dihidro-5-(trifluorometil)-3- isoxazolil]-2-metil-N-(cis-1-oxido-3-tietanil)benzamida, 4-[5-(3,5- diclorofenil)-4,5-dihidro-5-(trifluorometil)-3-isoxazolil]-2-metil-N-(trans-1- oxido-3-tietanil)benzamida e 4-[(5S)-5-(3,5-diclorofenil)-4,5-dihidro-5- (trifluorometil)-3-isoxazolil]-2-metil-N-(cis-1-oxido-3-tietanil)benzamida (conhecido através do documento WO 2013/050317 A1) (CAS 1332628-83-7), N-[3-cloro-1-(3-piridinil)-1H-pirazol-4-il]-N-etil-3-[(3,3,3- trifluoropropil)sulfinil]propanamida, (+)-N-[3-cloro-1-(3-piridinil)-1H- pirazol-4-il]-N-etil-3-[(3,3,3-trifluoropropil)sulfinil]propanamida and (-)-N- [3-cloro-1-(3-piridinil)-1H-pirazol-4-il]-N-etil-3-[(3,3,3-trifluoropropil) sulfinil]propanamida (conhecido através do documento WO 2013/162715 A2, WO 2013/162716 A2, US 2014/0213448 A1) (CAS 1477923-37-7), 5-[[(2E)-3-cloro-2-propen-1-il]amino]-1-[2,6-dicloro-4- (trifluorometil) fenil]-4-[(trifluorometil)sulfinil]-1H-pirazole-3-carbonitrile (conhecido através do documento CN 101337937 A) (CAS 110567277-2), 3-bromo-N-[4-cloro-2-metil-6-[(metilamino)tioxometil]fenil]-1-(3- cloro-2-piridinil)-1H-pirazole-5-carboxamida (Liudaibenjiaxuanan, conhecido através do documento CN 103109816 A) (CAS 123254385-9); N-[4-cloro-2-[[(1,1-dimetiletil)amino]carbonil]-6-metilfenil]-1-(3- cloro-2-piridinil)-3-(fluorometoxi)-1H-pirazole-5-carboxamida (conhecido através do documento WO 2012/034403 A1) (CAS 1268277-22-0), N-[2-(5-amino-1,3,4-tiadiazol-2-il)-4-cloro-6-metilfenil]- 3-bromo-1-(3-cloro-2-piridinil)-1H-pirazole-5-carboxamida (conhecido através do documento WO 2011/085575 A1) (CAS 1233882-22-8), 4- [3-[2,6-dicloro-4-[(3,3-dicloro-2-propen-1-il)oxi]fenoxi]propoxi]-2-metoxi- 6-(trifluorometil)pirimidine (conhecido através do documento CN 101337940 A) (CAS 1108184-52-6); (2E)- e 2(Z)-2-[2-(4-cianofenil)-1- [3-(trifluorometil)fenil] etilidene]-N-[4- (difluorometoxi)fenil]hidrazinecarboxamida (conhecido através do documento CN 101715774 A) (CAS 1232543-85-9); ciclopropanecarboxilic acid 3-(2,2-dicloroetenil)-2,2-dimetil-4-(1H- benzimidazol-2-il) fenil ester (conhecido através do documento CN 103524422 A) (CAS 1542271-46-4); (4aS)-7-cloro-2,5-dihidro-2- [[(metoxicarbonil)[4-[(trifluorometil)tio]fenil]amino]carbonil]indeno[1,2- e][1,3,4]oxadiazine-4a(3H)-carboxilic acid metil ester (conhecido através do documento CN 102391261 A) (CAS 1370358-69-2); 6- deoxi-3-O-etil-2,4-di-O-metil-1-[N-[4-[1-[4-(1,1,2,2,2- pentafluoroetoxi)fenil]-1H-1,2,4-triazol-3-il]fenil]carbamate]-α-L- mannopiranose (conhecido através do documento US 2014/0275503 A1) (CAS 1181213-14-8); 8-(2-ciclopropilmetoxi-4-trifluorometilfenoxi)- 3-(6-trifluorometilpiridazin-3-il)-3-azabiciclo[3.2.1] octane (CAS 1253850-56-4), (8-anti)-8-(2-ciclopropilmetoxi-4-trifluorometilfenoxi)-3- (6-trifluorometilpiridazin-3-il)-3-azabiciclo[3.2.1]octane (CAS 93379827-7), (8-syn)-8-(2-ciclopropilmetoxi-4-trifluorometilfenoxi)-3-(6- trifluorometilpiridazin-3-il)-3-azabiciclo[3.2.1]octane (conhecido através do documento WO 2007040280 A1, WO 2007040282 A1) (CAS 934001-66-8), N-[3-cloro-1-(3-piridinil)-1H-pirazol-4-il]-N-etil-3-[(3,3,3- trifluoropropil)tio]propanamida (conhecido através do documento WO 2015/058021 A1, WO 2015/058028 A1) (CAS 1477919-27-9) and N-[4- (aminotioxometil)-2-metil-6-[(metilamino)carbonil]fenil]-3-bromo-1-(3- cloro-2-piridinil)-1H-pirazole-5-carboxamida (conhecido através do documento CN 103265527 A) (CAS 1452877-50-7), 5-(1,3-dioxan-2- il)-4-[[4-(trifluorometil)fenil]metoxi]pirimidine (conhecido através do documento WO 2013/115391 A1) (CAS 1449021-97-9), 3-(4-cloro-2,6- dimetilfenil)-8-metoxi-1-metil-1,8-diazaspiro[4.5]decane-2,4-diona (conhecido através do documento WO 2014/187846 A1) (CAS 1638765-58-8), etil 3-(4-cloro-2,6-dimetilfenil)-8-metoxi-1-metil-2-oxo- 1,8-diazaspiro[4.5]dec-3-en-4-il-carboxilate (conhecido através do documento WO 2010/066780 A1, WO 2011151146 A1) (CAS 1229023-00-0), 4-[(5S)-5-(3,5-dicloro-4-fluorofenil)-4,5-dihidro-5- (trifluorometil)-3-isoxazolil]-N-[(4R)-2-etil-3-oxo-4-isoxazolidinil]-2- metilbenzamida (conhecido através do documento WO 2011/067272, WO2013/ 050302) (CAS 1309959-62-3).
[00121] Insecticidas que podem de preferência ser usados juntos com os herbicidas são, por exemplo, os seguintes: acetamiprid, acrinatrin, aldicarb, amitraz, acinfos-metila, ciflutrin, carbaril, cipermetrin, deltametrin, endosulfan, etoprofos, fenamifos, fention, fipronila, imidacloprid, metamidofos, metiocarb, niclosamida, oxidemeton-metila, protiofos, silafluofen, tiacloprid, tiodicarb, tralometrin, triazofos, triclorfon, triflumuron, terbufos, fonofos, forato, clorpirifos, carbofuran, teflutrin.
[00122] As combinações de compostos ativos de acordo com a invenção são adequados para o controle de um amplo espectro de ervas daninhas em terras não cultivadas, em caminhos, em vias férreas, em áreas industriais (“controle de ervas daninhas industriais) ou nas lavouras, tal como climas ou áreas geográficas temperados, subtropicais e tropicais. Exemplos de lavouras são dendezeiros, frutos secos (por exemplo, amêndoas, avelãs, nozes, macadâmia), coco, bagas, cítricos (por exemplo, laranja, limão, tangerina), banana, abacaxi, algodão, cana-de-açúcar, chá, afé, cacau, entre outras. Elas são igualmente adequadas para uso em pomicultura (por exemplo, frutas pomáceas tal como maçã, per, cereja, manga e kiwi) e viticultura. As preparações também podem ser usadas para semeadura (método de "burn-down", método de "no-till" ou método de "zero-till") ou para tratamento após a colheita (“alqueive” químico). Os possíveis usos das combinações de compostos ativos também se estendem ao controle de ervas daninhas no cultivo de árvores, cultivo de pinheiros jovens ou cultivo de eucalipto, em cada um dos casos antes do plantio ou depois do plantio (incluindo tratamento "over-top").
[00123] Também é possível usar as composições para o controle do crescimento de plantas indesejadas em culturas economicamente importantes tal como trigo (trigo duro e trigo mole), milho, soja, beterraba, cana-de-açúcar, algodão, arroz, feijões (por exemplo, vagem e feijão-fava), linho, cevada, aveia, centeio, triticale, batata e milhete/sorgo, terras não cultivadas, pastos e gramados/relvados e culturas de plantação. As culturas de plantação incluem frutos de pomo (maçã, pera, marmelo), bagas (amoras framboesa), cítricos, Prunus (cereja, nectarina, amêndoa), frutos secos (nozes, pecãs, avelã, castanha-de-caju, macadâmia), manga, cacau, café, uva (uva comestível, uva para vinhos), palmeiras (tal como dendezeiros, tamareiras, coqueiros), eucalipto, caqui, caqui, borracha, abacaxi, banana, abacat3e, lichia, culturas florestais (Eucalypteae, Piniaceae, Piceae, Meliaceae, etc.).
[00124] As combinações de compostos herbicidas ativos de acordo com a invenção, nas respectivas formas de uso (= composições herbicidas), apresentam sinergiais em relação à ação herbicida e seletividade, e ação favorável no que diz respeito ao espectro de ervas daninhas. Elas possuem excelente eficácia herbicida contra um amplo espectro de plantas daninhas anuais monocotiledôneas e dicotiledôneas economicamente importantes. Os compostos ativos também têm um bom controle sobre plantas daninhas perenes que são difíceis de controlar e produzem brotos a partir dos rizomas, raízes ou outros órgãos perenes.
[00125] Para aplicação, as combinações de compostos ativos podem ser aplicadas sobre as plantas (por exemplo, plantas daninhas tal como ervas daninhas monocotiledôneas ou dicotiledôneas ou plantas de lavoura indesejadas), sobre as sementes (por exemplo, grãos, sementes ou órgãos de propagação vegetativa tal como tubérculos ou partes de brotos com botões), ou sobre a área na qual as plantas crescem (por exemplo, a área de crescimento).
[00126] As substâncias podem ser aplicadas antes da semeadura (se apropriado, também por incorporação no solo), antes da emergência ou depois da emergência. Dá-se preferência ao uso pelo método logo após a semeadura e antes da emergência ou pelo método da pós-emergência nas plantas de lavoura contra plantas daninhas que ainda não emergiram ou que já emergiram. A aplicação também pode ser integrada em sistemas de controle de ervas daninhas com várias aplicações divididas (sequenciais).
[00127] Exemplos específicos de alguns representantes da flora monocotiledônea e dicotiledônea que podem ser controlados pelas combinações de compostos ativos de acordo com a invenção são as seguintes, embora a relação abaixo não se destine a impor qualquer restrição às espécies particulares.
[00128] No grupo das espécies de ervas daninhas monocotiledôneas, por exemplo, as espécies Aegilops, Agropyron, Agrostis, Alopecurus, Apera, Avena, Brachicaria, Bromus, Cynodon, Dactyloctenium, Digitaria, Echinochloa, Eleocharis, Eleusine, Eragrostis, Eriochloa, Festuca, Fimbristylis, Imperata, Ischaemum, Heteranthera, Imperata, Leptochloa, Lolium, Monochoria, Panicum, Paspalum, Phalaris, Phleum, Poa, Rottboellia, Sagittaria, Scirpus, Setaria, Sorghum, Sphenoclea e Cyperus estão cobertas pelo grupo anual.
[00129] No caso de espécies de ervas daninhas dicotiledôneas, o espectro de ação se estende a espécies tal como, por exemplo, Abutilon, Amaranthus, Ambrosia, Anoda, Anthemis, Aphanes, Artemisia, Atriplex, Bellis, Bidens, Capsella, Carduus, Cassia, Centaurea, Chenopodium, Cirsium, Convolvulus, Datura, Desmodium, Emex, Erodium, Erysimum, Euphorbia, Galeopsis, Galinsoga, Galium, Geranium, Hibiscus, Ipomoea, Kochia, Lamium, Lepidium, Lindernia, Matricaria, Mentha, Mercurialis, Mullugo, Myosotis, Papaver, Pharbitis, Plantago, Polygonum, Portulaca, Ranunculus, Raphanus, Rorippa, Rotala, Rumex, Salsola, Senecio, Sesbania, Sida, Sinapis, Solanum, Sonchus, Sphenoclea, Stellaria, Taraxacum, Thlaspi, Trifolium, Urtica, Veronica, Viola, Xanthium.
[00130] Se as combinações de compostos ativos de acordo com a invenção forem aplicadas à superfície do solo antes da germinação, ou a emergência de plântulas de ervas daninhas é completamente prevenida ou as ervas daninhas crescem até atingirem o estágio cotilédone, mas então param de crescer e finalmente morrem completamente depois de passadas três ou quatro semanas.
[00131] Se os compostos ativos forem aplicados em pós- emergência às partes verdes das plantas, o crescimento é interrompido depois do tratamento, e as plantas daninhas permanecem no estágio de crescimento no momento da aplicação, ou morrem completamente depois de um certo tempo, de modo que desta maneira a competição pelas ervas daninhas, que são prejudiciais às plantas de lavoura, é eliminada muito cedo e de forma ininterrupta.
[00132] As composições herbicidas de acordo com a invenção são notáveis pelo início rápido e longa duração da ação herbicida. Em geral, a resistência à chuva dos compostos ativos nas combinações de acordo com a invenção é favorável. Uma vantagem particular é que as dosagens eficazes dos compostos (A) e (B) que são usados nas combinações podem ser ajustadas em um nível tão baixo que sua ação no solo é idealmente baixa. Portanto, o uso das mesmas em culturas sensíveis não só é permitido, como também a contaminação do fluxo de águas subterrâneas é virtualmente prevenida. A combinação de compostos ativos de acordo com a invenção permite que a taxa de aplicação requerida dos compostos ativos seja considervalmente reduzida.
[00133] O uso combinado dos herbicidas (A) e (B) alcança propriedades de desempenho que vão além daquilo que seria esperado das propriedades conhecidas dos herbicidas individuais para a combinação dos mesmos. Por exemplo, os efeitos herbicidas para uma espécie de planta daninha particular ultrapassa o valor esperado que pode ser estimado por métodos tradicionais, por exemplo, de acordo com o método de Colby ou outros métodos de extrapolação.
[00134] Haverá um efeito sinergístico sempre que o efeito, aqui o efeito herbicida, das combinações de compostos ativos for maior que a soma total dos efeitos dos compostos ativos aplicados individualmente. A atividade esperada para uma dada combinação de dois compostos ativos pode ser calculada de acordo com S.R. Colby (“Calculating Synergistic and Antagonistic Responses of Herbicide Combinations”, Weeds 15 (1967), 20-22) (vide abaixo).
[00135] Portanto, os efeitos sinergísticos permitem, por exemplo, uma redução nas taxas de aplicação dos compostos ativos individuais, uma maior eficácia à mesma taxa de aplicação, o controle de espécies de plantas daninhas que ainda não estão cobertas (lacunas), ação residual elevada, um período de eficácia prolongado, uma alta velocidade de ação, uma extensão do período de aplicação e/ou uma redução no número de aplicações individuais e - como resultado para o usuário - sistemas de controle de ervas daninhas que são econômica e ecologicamente vantajosos.
[00136] Embora as combinações de acordo com a invenção tenham excelente atividade herbicida para ervas daninhas monocotiledôneas e dicotiledôneas, muitas plantas de lavoura economicamente importantes, dependendo da estrutura das respectivas combinações de compostos ativos de acordo com a invenção e da taxa de aplicação das mesmas, serão danificadas ainda que de forma insignificante, se forem. Culturas economicamente importantes aqui são, por exemplo, culturas dicotiledôneas dos gêneros Arachis, Beta, Brassica, Cucumis, Cucurbita, Helianthus, Daucus, Glycine, Gossypium, Ipomoea, Lactuca, Linum, Lycopersicon, Nicotiana, Phaseolus, Pisum, Solanum, Vicia, ou culturas monocotiledôneas dos gêneros Allium, Ananas, Asparagus, Avena, Hordeum, Oryza, Panicum, Saccharum, Secale, Sorghum, Triticale, Triticum e Zea.
[00137] Além disso, as composições de acordo com a invenção apresentam em alguns casos propriedades reguladoras do crescimento extraordinárias nas plantas de lavoura. Eles interferem no metabolismo próprio das plantas com efeito regulador, e podem, portanto, ser usadas para influenciar de forma controlada os constituintes das plantas e facilitar a colheita, por exemplo, desencadeando o dessecamento e o crescimento atrofiado. Além disso, elas também são adequadas para o controle geral e a inibição do crescimento vegetativo indesejado sem destruir as plantas no processo. A inibição do crescimento vegetativo tem um papel importanto para muitas culturas monocotiledôneas e dicotiledôneas já que isto pode reduzir ou impedir completamente o alojamento.
[00138] Devido as suas propriedades herbicidas e reguladores do crescimento de plantas, as composições podem descritas para o controle de plantas daninhas em plantas de lavoura conhecidas ou em plantas de lavoura tolerantes ainda a serem desenvolvidas que tenham sido modificadas por mutagênese convencional ou geneticamente modificadas. Em geral, as plantas transgênicas distinguem-se por propriedades específicas vantajosas, além de resistência às composições de acordo com a invenção, por exemplo, por resistência a doenças de plantas ou aos organismos causadores de doenças de plantas tal como determinados insetos ou microorganismos, tal como fungos, bactérias ou vírus. Outras propriedades particulares se referem, por exemplo, ao material colhido em termos de quantidade, qualidade, armazenabilidade, composição e constituintes específicos. Por exemplo, existem plantas transgênicas conhecidas com um teor de amido elevado ou com a qualidade do amido alterado, ou aquelas com uma composição de ácidos graxos diferente no material colhido. Outras propriedades particulares podem ser tolerância ou resistência a estressores abióticos, por exemplo, calor, temperaturas baixas, seca, salinidade e radiação ultravioleta.
[00139] De preferência, as combinações de compostos ativos de acordo com a invenção podem ser usadas como herbicidas em culturas de plantas de lavoura que são resistentes, ou que foram tornadas resistentes por engenharia genética, aos efeitos fitotóxicos dos herbicidas.
[00140] Maneiras convencionais de produção de novas plantas que têm propriedades modificadas em relação às plantas existentes consistem, por exemplo, em métodos de cultivo tradicionais e na geração de mutantes. Alternativamente, novas plantas com propriedades modificadas podem ser geradas com o auxílio de métodos recombinantes (vide, por exemplo, os documentos EP-A- 0221044, EP-A-0131624). Por exemplo, há descrições em diversos casos de: - modificações genéticas de plantas de lavoura com a finalidade de modificar o amido sintetizado nas plantas (por exemplo, documentos WO 92/11376, WO 92/14827, WO 91/19806), - plantas de lavoura transgênicas que apresentam resistência a outros herbicidas, por exemplo, a sulfonilureias (documentos EP-A-0257993, US-A-5013659), - plantas de lavoura transgênicas com capacidade de produzir toxinas de Bacillus thuringiensis (Bt toxins), que tornam as plantas resistentes a pragas específicas (documentos EP-A-0142924, EP-A-0193259), - plantas de lavoura transgênicas com uma composição de ácidos graxos modifiada (documento WO 91/13972), - plantas de lavoura geneticamente modificadas com novos constituintes ou metabólitos secundários, por exemplo, novas fitoalexinas, que criam maior resistência a doenças (documentos EPA 309862, EPA0464461), - plantas geneticamente modificadas com fotorrespiração reduzida, que têm rendimentos mais altos e maior tolerância ao estresse (documento EPA 0305398), - plantas de lavoura transgênicas que produzem proteínas farmaceuticamente ou diagnosticamente importantes ("agrofarmacêutica molecular"), - plantas de lavoura transgênicas que apresentam rendimentos mais altos ou melhor qualidade, - plantas de lavoura transgênicas que apresentam uma combinação, por exemplo, das novas propriedades mencionadas acima ("estaqueamento de genes").
[00141] Numerosas técnicas de biologia molecular que podem ser usadas para produzir novas plantas transgênicas com propriedades modificadas são, a princípio, conhecidas; vide, por exemplo, I. Potrykus and G. Spangenberg (eds.) Gene Transfer to Plants, Springer Lab Manual (1995), Springer Verlag Berlin, Heidelberg, ou Christou, "Trends in Plant Science" 1 (1996) 423-431.
[00142] Para tais manipulações recombinantes, moléculas de ácido nucleico que possibilitam a mutagênese ou a alteração de sequências por recombinação de sequênciaas de DNA podem ser introduzidas em plasmídeos. Com o auxílio de métodos tradicionais, é possível, por exemplo, fazer substituições de bases, remover partes de sequências ou adicionar sequências naturais ou sintéticas. Para unir os fragmentos de DNA uns com outros, adaptadores ou ligantes podem ser colocados sobre os fragmentos, vide, por exemplo, Sambrook et al., 1989, Molecular Cloning, A Laboratory Manual, 2nd edition Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY; ou Winnacker "Gene und Klone" ["Genes and clones"], VCH Weinheim 2nd edition 1996.
[00143] Por exemplo, a geração de células vegetais com uma atividade reduzida de um produto genético pode ser obtida por expressão de pelo menos um RNA antisense correspondente, um RNA sense para obter um efeito de cossupressão, ou por expressão de pelo menos uma ribozima construída de forma adequada que cliva especificamente transcritos do produto genético mencionado acima.
[00144] Para tanto, em primeiro lugar, é possível usar moléculas de DNA que abrangem a sequência codificadora inteira de um produto genética, inclusive de quaisquer sequências flanqueadoras que possam estar presentes, e também moléculas de DNA que abrangem apenas partes da sequência codificadora, em cujo caso é necessário que essas partes sejam suficientemente longas para terem um efeito antisense nas células. Também é possível usar sequências de DNA que possuem um alto grau de homologia com as sequências codificadoras de um produto genético, mas que não são totalmente idênticas às mesmas.
[00145] Ao se expressar moléculas de ácido nucleico em plantas, a proteína sintetizada pode ficar localizada em qualquer compartimento desejado da célula vegetal. No entanto, para obter uma localização em um compartimento específico, é possível, por exemplo, unir a região codificadora a sequências de DNA que garantam a localização em um compartimento específico. Tais sequências são conhecidas pelos especialistas na técnica (vide, por exemplo, Braun et al., EMBO J. 11 (1992), 3219-3227; Wolter et al., Proc. Natl. Acad. Sci. USA 85 (1988), 846-850; Sonnewald et al., Plant J. 1 (1991), 95-106). As moléculas de ácido nucleico também podem ser expressas nas organelas das células vegetais.
[00146] As células de plantas transgênicas podem ser regeneradas por técnicas conhecidas para dar origem a plantas inteiras. A princípio, as plantas transgênicas podem ser plantas de qualquer espécie vegetal desejada, i.e., não só plantas monocotiledôneas como também plantas dicotiledôneas. Assim sendo, pode-se obter plantas transgênicas cujas propriedades são alteradas por superexpressão, supressão ou inibição de genes ou sequências genéticas homólogas (= naturais) ou expressão de genes ou sequências genéticas heterólogas (= estranhas).
[00147] As combinações de compostos ativos de acordo com a invenção podem ser de preferência usadas em culturas transgênicas que são tolerantes ou foram tornadas tolerantes aos compostos ativos usados.
[00148] As combinações de compostos ativos de acordo com a invenção também podem ser de preferência usadas em culturas transgênicas que são resistentes a reguladores do crescimento tal como, por exemplo, dicamba, ou a herbicidas que inibem enzimas vegetais essenciais, por exemplo, acetolactato sintases (ALS), EPSP sintases, glutamina sintases (GS) ou hidroxifenilpiruvato dioxigenases (HPPD), ou a herbicidas do grupo das sulfonilureias, dos glifosatos, glufosinatos ou benzoilisoxazóis e compostos ativos análogos.
[00149] A invenção, portanto, também apresenta um método para o controle do crescimento de plantas indesejadas, opcionalmente em culturas de plantas de lavoura, de preferência em terras não cultivadas ou em plantações, caracterizado pelo fato de que um ou mais herbicidas do tipo (A) é/são aplicados com um ou mais herbicidas do tipo (B) às plantas de lavoura, partes das plantas ou sementes das plantas (sementes) das mesmas ou à área de crescimento.
[00150] A invenção também apresenta o uso das novas combinações de compostos (A)+(B) para o controle de plantas daninhas, opcionalmente em culturas de plantas de lavoura, de preferência em áreas não cultivadas e plantações, mas também para o controle de plantas daninhas antes da semeadura da planta de lavoura subsequente, tal como, em particular, para preparação para semeadura ("aplicação burn-down").
[00151] As combinações de compostos ativos de acordo com a invenção podem ser produzidas seja como formulações mistas dos dois componentes, se apropriado com outros compostos ativos, aditivos e/ou auxiliares de formulação usuais presentes, que são então aplicadas de maneira usual diluídas com água, ou podem ser produzidas como as chamadas misturas de tanque por diluição conjunta dos componentes formulados separadamente ou parcialmente formulados separadamente com água.
[00152] Os compostos (A) e (B) ou suas combinações podem ser formulados de várias maneiras sgundo as quais parâmetros biológicos e/ou físico-químicos são necessários. Exemplos de opções gerais são: pós umectáveis (WP), pós hidrossolúveis (SP), concentrados emulsificáveis (EC), concentrações hidrossolúveis, soluções aquosas (SL), emulsões (EW) tal como emulsões de óleo em água e de água em óleo, soluções ou emulsões espalháveis, dispersões à base de óleo ou de água, dispersões oleosas (OD), suspoemulsões, suspensões concentradas (SC), soluções miscíveis em óleo, suspensões de cápsulas (CS), produtos para polvilhamento (DP), agentes de revestimento de sementes, grânulos para aplicação ao solo ou espalhamento, grânulos (GR) na forma de microgrânulos, grânulos para pulverização, grânulos de absorção e grânulos de adsorção, grânulos dispersíveis em água (WG), grânulos hidrossolúveis (SÍLICA GEL), formulações ULV, microcápsulas ou ceras.
[00153] A invenção também apresenta, portanto, composições herbicidas e reguladores do crescimento de plantas que compreendem as combinações de compostos ativos de acordo com a invenção.
[00154] Os tipos de formulação individuais são a princípio conhecidos e estão descritos, por exemplo, em: Winnacker-Küchler, "Chemische Technologie" ["Chemical technology"], Volume 7, C. Hanser Verlag Munich, 4th Ed. 1986, van Valkenburg, "Pesticide Formulations", Marcel Dekker, N.Y., 1973; K. Martens, "Spray Drying Handbook", 3rd Ed. 1979, G. Goodwin Ltd. London.
[00155] Os auxiliares de formulação necessários, tal como materiais inertes, tensoativos, solventes e outros aditivos, são igualmente conhecidos e estão descritos, por exemplo, em: Watkins, "Handbook of Insecticide Dust Diluents and Carriers", 2nd Ed., Darland Books, Caldwell N.J., H.v. Olphen, "Introduction to Clay Colloid Chemistry"; 2nd Ed., J. Wiley & Sons, N.Y., C. Marsden, "Solvents Guide", 2nd Ed., Interscience, N.Y. 1963; McCutcheon's "Detergents and Emulsifiers Annual", MC Publ. Corp., Ridgewood N.J.; Sisley and Wood, "Encyclopedia of Surface Active Agents", Chem. Publ. Co. Inc., N.Y. 1964, Schonfeldt, "Grenzflachenaktive Ãthylenoxidaddukte" ["Interfaceactive Ethylene Oxide Adducts"], Wiss. Verlagsgesellschaft, Stuttgart 1976, Winnacker-Küchler, "Chemische Technologie" ["Chemical Technology"], Volume 7, C. Hanser Verlag Munich, 4th Ed. 1986.
[00156] Com base nessas formulações, também é possível produzir combinações com outras substâncias pesticidamente ativas, tal como outros herbicidas, fungicidas, inseticidas ou outros pesticidas (por exemplo, acaricidas, nematicidas, moluscicidas, rodenticidas, aficidas, avicidas, larvicidas, ovicidas, bactericidas, virucidas, etc.), e protetores, fertilizantes e/ou reguladores do crescimento, por exemplo, na forma de uma formulação pronta para uso ou como uma mistura de tanque.
[00157] Pós umectáveis são preparações que podem ser uniformemente dispersadas em água e, além do composto ativo, fora um diluente ou uma substância inerte, também compreendem tensoativos do tipo iônico e/ou não iônico (agentes umectantes, dispersantes), por exemplo, alquil fenóis polioxietilados, álcoois graxos polioxietilados, aminas graxas polioxietiladas, sulfatos de éter poliglicólico de álcoois graxos, alcanossulfonatos, alquil benzenossulfonatos, lignossulfonato de sódio, 2,2'-dinaftilmetano-6,6'- dissulfonato de sódio, dibutilnaftalenossulfonato de sódio ou ainda oleoilmetiltaurato de sódio. Para produzir os pós umectáveis, os compostos herbicidas ativos são finamente moídos, por exemplo, em aparelhos usuais tal como moinhos de martelo, moinhos de sopro e moinhos de jato de ar, e simultaneamente ou subsequentemente misturados com os auxiliares de formulação.
[00158] Concentrados emulsificáveis são produzidos por dissolução do composto ativo em um solvente orgânico, por exemplo, butanol, ciclo-hexanona, dimetilformamida, xileno, ou ainda aromáticos ou hidrocarbonetos de ponto de ebulição relativamente alto ou misturas de solventes orgânicos, com adição de um ou mais tensoativos iônicos e/ou não iônicos (emulsificantes). Exemplos de emulsificantes que podem ser usados são sais de alquilarilsulfonato de cálcio, tal como dodecilbenzenossulfonato de cálcio, ou emulsificantes não iônicos tal como ésteres poliglicólicos de ácidos graxos, éteres alquilaril poliglicólicos, éteres poliglicólicos de álcoois graxos, produtos da condensação de óxido de propileno-óxido de etileno, alquil poliéteres, ésteres de sorbitan, por exemplo ésteres de ácidos graxos de sorbitan, ou, por exemplo, ésteres de ácidos graxos de polioxietileno sorbitan.
[00159] Os produtos para polvilhamento são obtidos por moagem do composto ativo com sólidos finamente distribuídos, por exemplo, talco, argilas naturais, tal como caulim, bentonita e pirofilita, ou terra diatomácea.
[00160] As suspensões concentradas podem ser à base de água ou de óleo. Elas podem ser preparadas, por exemplo, por moagem por via úmica por meio de moinhos de bola comerciais e adição opcional de tensoativos tal como, por exemplo, aqueles já listados acima para outros tipos de formulação.
[00161] As emulsões, por exemplo, emulsões de óleo em água (EW), podem ser produzidas, por exemplo, por meio de agitadores, moinhos coloidas e/ou misturadores estáticos usando solventes orgânicos aquosos e opcionalmente tensoativos tal como, por exemplo, aqueles já listados acima para outros tipos de formulação.
[00162] Os grânulos podem ser preparados seja por aspersão do composto ativo sobre material inerte granular capaz de adsorção ou por aplicação de concentrados do composto ativo à superfície de substâncias carreadoras, tal como areia, caulinitas, ou de material inerte granular por meio de adesivos, por exemplo, álcool polivinílico, poliacrilato de sódio ou óleos minerais. Os compostos ativos adequados também podem ser granulados da maneira usual para a produção de grânulos de fertilizante - se desejado como uma mistura com fertilizantes.
[00163] Os grânulos dispersíveis em água geralmente são produzidos por processos tal como secagem por aspersão, granulação em leito fluidificado, granulação em tacho, misturação com misturadores de alta velocidade e extrusão sem material inerte sólido.
[00164] As preparações agroquímicas geralmente compreendem de 0,1 a 99% em peso, em particular de 0,2 a 95% em peso, de compostos ativos dos tipos (A) e/ou (B), as seguintes concentrações sendo usuais, dependendo do tipo de formulação:
[00165] Nos pós umectáveis, a concentração de composto ativo varia, por exemplo, de cerca de 10% a 95% em peso, o restante para 100% em peso consistindo em constituintes de formulação usuais. No caso de concentrados emulsificáveis, a concentração de composto ativo pode variar de cerca de 1% a 90% em peso, de preferência 5 a 80 por cento em peso.
[00166] Formulações na forma de polvilhos usualmente contêm 5% a 20% em peso de composto ativo; soluções borrifáveis contêm cerca de 0,05 a 80, de preferência 2 a 50, por cento em peso (% em peso) de composto ativo.
[00167] No caso de grânulos tal como grânulos dispersíveis, o teor de composto ativo depende em parte do fato de o composto ativo estar presente na forma líquida ou sólido e de quais auxiliares de granulação e cargas são usados. Em geral, o teor nos grânulos dispersíveis em água varia entre 1% e 95% em peso, de preferência entre 10% e 80% em peso.
[00168] Além disso, as formulações de composto ativo mencionadas opcionalmente compreendem os respectivos adesivos, agentes umectantes, dispersantes, emulsificantes, penetrantes, consrevantes, agentes anticongelamento e solventes, cargas, colorantes e carreadores, antiespumantes, inibidores de evaporação e composições modificadoras do pH ou da viscosidade usuais.
[00169] Para aplicação, as formulações na forma comercial são, se apropriado, diluídas da maneira usual, por exemplo, no caso de pós umectáveis, concentrados emulsificáveis, dispersões e grânulos dispersíveis em água com água. Preparaçõees do tipo polvilho, grânulos para aplicação ao solo ou espalhamento e soluções borrifáveis normalmente não são diluídas com outras substâncias inertes antes da aplicação.
[00170] Os compostos ativos podem ser aplicados às plantas, partes das plantas, sementes das plantas ou à área sendo cultivada (solo), de preferência às plantas verdes e partes das plantas, e opcionalmente adicionalmente ao solo.
[00171] Um uso possível é a aplicação conjunta dos compostos ativos na forma de misturas de tanque, onde formulações concentradas formuladas de forma ideal dos compostos ativos individuais são, juntas, misturadas em um tanque com água, e o licor de borrifação obtido é aplicado.
[00172] Uma formulação herbicida conjunta da combinação inventiva de compostos ativos (A) e (B) apresenta a vantagem de poder ser aplicada de forma mais fácil uma vez que as quantidades dos componentes já estão ajustadas na proporção correta. Ademais, os auxiliares na formulação podem ser ajustados um ao outro de forma ideal, ao passo que uma mistura de tanque de diferentes formulações pode resultar em combinações indesejadas dos auxiliares. A. Exemplos de formulações genéricas a) Um produto para polvilhamento é obtido por misturação de 10 partes em peso de um composto ativo (A) ou (B) ou de uma mistura de compostos ativos (A) + (B) (e opcionalmente outros compostos ativos componentes) e/ou sais dos mesmos e 90 partes em peso de talco como substância inerte, e cominuição em um moinho de batedeira. b) Um pó umectável que é facilmente dispersível em água é obtido por misturação de 25 partes em peso de um composto ativo/mistura de compostos ativos, 64 partes em peso de quartzo contendo caulim como substância inerte, 10 partes em peso de lignossulfonato de potássio e 1 parte em peso de oleoilmetiltaurato de sódio como agente umectante e dispersante, e moagem da mistura em um moinho de discos fixos. c) Uma dispersão concentrada que é facilmente dispersível em água é obtida por misturação de 20 partes em peso de um composto ativo/mistura de compostos ativos com 6 partes em peso de éter alquil fenol poliglicólico (Triton® X 207), 3 partes em peso de éter isotridecanol poliglicólico (8 EO) e 71 partes em peso de óleo mineral parafínico (faixa de ebulição, por exemplo, aproximadamente 255 a 277°C) e moagem da mistura em um moinho de bolas de atrito até uma finura abaixo de 5 microns. d) Um concentrado emulsificável é obtido a partir de 15 partes em peso de um composto ativo/mistura de compostos ativos, 75 partes em peso de ciclo-hexanona como solvente e 10 partes em peso de nonilfenol etoxilado como emulsificante. e) Grânulos dispersíveis em água são obtidos por misturação de 75 partes em peso de um composto ativo/mistura de compostos ativos, 10 partes em peso de lignossulfonato de cálcio, 5 partes em peso de lauril sulfato de sódio, 3 partes em peso de álcool polivinílico e 7 partes em peso de caulim, moagem da mistura em um moinho de discos fixos, e granulação do pó em leito fluidificado pela aplicação de água borrifada como líquido de granulação. f) Grânulos dispersíveis em água também são obtidos por homogeneização e pré-cominuição, em um moinho coloidal, de 25 partes em peso de um composto ativo/mistura de compostos ativos, 5 partes em peso de 2,2'-dinaftilmetano-6,6'-disulfonato de sódio, 2 partes em peso de oleoilmetiltaurato de sódio, 1 part em peso de álcool polivinílico, 17 partes em peso de carbonato de cálcio e 50 partes em peso de água, e então moagem da mistura em um moinho de contas e atomização e secagem da suspensão resultante em uma torre de borrifação por meio de um bico de fase única.
[00173] Com a aplicação das combinações de acordo com a invenção, os efeitos herbicidas em uma espécie de planta daninha que excede a soma total formal dos efeitos dos herbicidas presentes onde aplicados isoladamente foram observados com frequência. Alternativamente, em alguns casos, é possível observar que é necessária uma taxa de aplicação mais baixa para a combinação herbicida para obtenção do mesmo efeito para uma espécie de planta daninha comparada às preparações individuais. Tais aumentos na ação ou aumentos na eficácia ou reduções na taxa de aplicação são uma forte indicação de um efeito sinergístico.
[00174] Quando as eficácias observadas já excedem a soma total formal dos valores dos testes com aplicações individuais, elas também excedem o valor esperado segundo Colby, que é calculado por meio da fórmula abaixo e é igualmente considerado uma indicação de sinergismo (cf. S. R. Colby; in Weeds 15 (1967) págs. 20 a 22): EC = A+B - (A-B/100) onde: A = eficácia do composto ativo (A) em % a uma taxa de aplicação de a g i.a./ha; B = eficácia do composto ativo (B) em % a uma taxa de aplicação de b g i.a./ha; EC = valor esperado do efeito da combinação (A)+(B) em % à taxa de aplicação combinada a+b g i.a./ha.
[00175] Os valores observados (EA) a partir das baixas dosagens adequadas dadas nos experimentos demonstram um efeito das combinações que excede os valores esperados segundo Colby (Δ).
[00176] Sementes ou pedaços de rizoma de ervas daninhas monocolitedôneas e dicotiledôneas são colocados em argila arenosa em vasos, cobertos com terra e cultivados em uma estufa em boas condições de crescimento (temperatura, umidade do ar, abastecimento de água). Três semanas após a semeadura, as plantas de teste são tratadas no estágio de três folhas com as composições de acordo com a invenção. As composições de acordo com a invenção formuladas composição pós borrifáveis ou como concentrados de emulsão são borrifadas sobre as partes verdes das plantas em várias dosagens com uma taxa de aplicação de 300 a 800 L/ha de água (equivalente). Depois que as plantas de testes foram deixadas descansando na estufa em condições de crescimento ideais por cerca de 3 a 4 semanas, a ação das preparações foi avaliada visualmente em comparação com os controles não tratados. As composições de acordo com a invenção também possuem boa atividade herbicida em pós-emergência contra um amplo espectro de gramíneas daninhas e ervas daninhas de folhas largas economicamente importantes.
[00177] Os efeitos das combinações de acordo com a invenção que excedem a soma total formal dos efeitos no caso de aplicação individual dos herbicidas são frequentemente observados aqui. Os valores observados a partir das baixas dosagens adequadas dadas nos experimentos demonstram um efeito das combinações que excede os valores esperados segundo Colby.
[00178] Os experimentos foram conduzidos em lotes de terra externos de acordo com a invenção as condições em estufa da seção 1. A avaliação foi análoga àquela dos experimentos da seção 1.
[00179] Plantas de lavoura foram cultivadas em lotes de terra externos em condições externas naturais, com a colocação de sementes ou pedaços de rizoma de plantas daninhas típicas ou com a utilizada da flora natural de ervas daninhas. O tratamento com as composições de acordo com a invenção foi efetuado depois as plantas daninhas e as plantas de lavoura terem emergido, geralmente no estágio de 2 a 4 folhas; em alguns casos (conforme especificado), compostos ativos individuais ou combinações de compostos ativos foram aplicados em pré-emergência ou como um tratamento sequencial parte em pré- emergência e/ou em pós-emergência.
[00180] No caso de culturas de plantação, em geral, somente o solo entre as plantas de lavoura individuais foi tratado com os compostos ativos.
[00181] Depois da aplicação, por exemplo, 2, 4, 6 e 8 semanas depois da aplicação, o efeito das preparações foi avaliado visualmente por comparação com os controles não tratados. As composições de acordo com a invenção também têm atividade herbicida sinergística em experiências de campo contra um amplo espectro de gramíneas daninhas e ervas daninhas de folhas largas economicamente importantes. A comparação mostrou que as combinações de acordo com a invenção normalmente possuem ação herbicida maior, e em alguns casos consideravelmente maior, que a soma total dos efeitos dos herbicidas individuais e, por conseguinte, sugere sinergismo. Os efeitos em partes significativas do período de avaliação também estavam acima dos valores esperados segundo Colby, e, por conseguinte, também sugerem sinergismo. As plantas de lavoura, ao contrário, sofreram apenas danos insignificantes, se é que sofreram algum, como resultado dos tratamentos com as composições herbicidas.
[00182] As seguintes abreviações são usadas na descrição e nas tabelas que se seguem: g i.a./ha = gramas de substância ativa (ingrediente ativo) (= 100% de composto ativo) por hectare;
[00183] A soma total dos efeitos das aplicações individuais está apresentada no item EA;
[00184] Cada um dos valores esperados segundo Colby está apresentado no item EC.
[00185] Os resultados biológicos das composições de acordo com a invenção estão resumidos nas Tabelas 3.1-3.2. O período de avaliação está apresentado em dias após a aplicação (DAT). Tabela 3.1: Efeito sinergístico (Δ) de composições herbicidas binárias compreendendo herbicidas do grupo B2, aplicados pelo método da pós-emergência
Tabela 3.2: Efeito sinergístico de composições herbicidas binárias compreendendo herbicidas do grupo B7, aplicados applied pelo método da pós-emergência
Claims (11)
1. Composição herbicida, caracterizada pelo fato de que compreende os compostos herbicidamente ativos (A) e (B), sendo queo Componente (A) é selecionado dentre: A1, A2, A3, A4 e A5, ou um sal agroquimicamente compatível desses compostos, sendo que A1-A5 apresentam as seguintes definições:
e sendo que o Componente (B) selecionado dentre: (B7.(4) Glufosinato (B2.18) Diflufenican, (B7.(5) Glifosato.
2. Composição herbicida, de acordo a reivindicação 1, caracterizada pelo fato de que compreende os compostos ativos Componentes (A) e (B) em uma razão em peso de 1:15000 a 500:1.
3. Composição herbicida, de acordo com a reivindicação 1 ou 2, caracterizada pelo fato de que compreende um ou mais outros componentes do grupo que compreende outros tipos de compostos protetores de lavoura ativos.
4. Agente herbicida, caracterizado pelo fato de que compreende a composição herbicida, como definida em qualquer uma das reivindicações 1 a 3, compreendendo um ou mais aditivos usuais na proteção de lavouras.
5. Método para controlar plantas daninhas ou para regular o desenvolvimento de plantas, caracterizado pelo fato de que componentes de compostos ativos da composição herbicida, como definida em qualquer uma das reivindicações 1 a 3, são aplicados às plantas, partes das plantas, sementes das plantas ou à área sendo cultivada.
6. Método, de acordo com a reivindicação 5, caracterizado pelo fato de que os componentes de compostos ativos da composição herbicida são aplicados pelo método da pré-emergência, pelo método da pós-emergência ou pelo método da pré- e pós-emergência às plantas, partes das plantas, sementes das plantas ou à área sendo cultivada.
7. Método, de acordo com a reivindicação 6, caracterizado pelo fato de que o componente herbicida (A) é aplicado a uma taxa de aplicação de 0,01 a 1000 g i.a./ha.
8. Método, de acordo com a reivindicação 6, caracterizado pelo fato de que o componente herbicida (B) é aplicado a uma taxa de aplicação de 0,01 a 4000 g i.a./ha.
9. Método, de acordo com qualquer uma das reivindicações 6 a 8, caracterizado que é para controle de plantas daninhas por tratamento antes da semeadura das plantas de lavoura e em áreas de cultivo, e também em terras não cultivadas.
10. Método, de acordo com qualquer uma das reivindicações 6 a 9, caracterizado pelo fato de que os compostos ativos da composição herbicida são aplicados na forma de uma composição herbicida compreendendo um ou mais aditivos usuais na proteção de lavouras, opcionalmente depois de diluídos em água.
11. Uso da composição herbicida, como definida em qualquer uma das reivindicações 1 a 3, caracterizado pelo fato de que é para controlar plantas daninhas ou para regular o crescimento de plantas.
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