BRPI0719027A2 - Formulação, métodos de combater insetos nocivos e/ou fungos fitopatogênicos, e de controlar vegetação indesejada, e, sementes - Google Patents
Formulação, métodos de combater insetos nocivos e/ou fungos fitopatogênicos, e de controlar vegetação indesejada, e, sementes Download PDFInfo
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- BRPI0719027A2 BRPI0719027A2 BRPI0719027-1A BRPI0719027A BRPI0719027A2 BR PI0719027 A2 BRPI0719027 A2 BR PI0719027A2 BR PI0719027 A BRPI0719027 A BR PI0719027A BR PI0719027 A2 BRPI0719027 A2 BR PI0719027A2
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- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
- LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 description 1
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 description 1
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 description 1
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical group 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
- 150000003556 thioamides Chemical class 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical group COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- 235000010215 titanium dioxide Nutrition 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
- 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
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 150000004669 very long chain fatty acids Chemical class 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 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
- 229910052726 zirconium Inorganic materials 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Toxicology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Catching Or Destruction (AREA)
Description
"FORMULAÇÃO, MÉTODOS DE COMBATER INSETOS NOCIVOS E/OU FUNGOS FITOPATOGÊNICOS, DE CONTROLAR VEGETAÇÃO INDESEJADA, E, SEMENTES"
A presente invenção diz respeito a uma formulação que compreende
(a) pelo menos um pesticida e
(b) pelo menos um tensoativo não iônico da fórmula I
R1-O-(AO)x-(H) (I)
em que
R1 representa alquila de cadeia reta ou ramificada tendo de 4 a
átomos de carbono;
AO é etilenoóxi, propilenoóxi ou uma mistura de etilenoóxi e
propilenoóxi e
χ corresponde aos valores de 2 a 30 e
(c) pelo menos um alcoilato de tristirilfenila iônico e
(d) pelo menos um óleo e
(e) água,
em que o pesticida está presente na fase aquosa na forma de uma suspensão e o óleo é essencialmente isento de pesticida.
As formulações agrícolas que compreendem tristirilfenóis alcoxilados são conhecidos. O WO 2006/114186 divulga suspoemulsões água em óleo, em que a fase oleosa compreende o pesticida, O EP 0514769 divulga suspoemulsões que compreende um herbicida, um solvente aromático e tristirilfenóis etoxilados. O termo suspoemulsões é definido neste de acordo com Mulqeen et al., Pesticida Science, 1990, 29, 451-465 como combinação de "uma fase de emulsão, contendo um ou mais ingredientes ativos, com uma fase contínua também contendo um de mais ingredientes ativos na forma de uma dispersão sólida." US 6.664.213 Bl descreve uma composição pesticida líquida compreendendo um ingrediente ativo pesticidamente e um polioxaetileno éter que tem um valor HLB de 6 13,5 e um teor de 10 a 50% baseado na composição. WO 00/78139 descreve uma composição herbicida líquida contendo um tensoativo aniônico carfentrazona-etila, um composto orgânico solúvel em água e água e tendo um pH de 2 a 7.
Um dos objetivos do químico de formulação está voltado ao desenvolvimento de formulações, em que os ativos são mantidos em suspensão estável. Um outro objetivo que é desejável para muitas aplicações na proteção de planta é fornecer uma formulação, que seja capaz de manter mais do que um ativo dispersado ou que seja capaz de manter um par de ativos em suspensão e pelo menos um óleo emulsificado no mesmo meio.
O objetivo foi resolvido por uma formulação que compreende (a) pelo menos um pesticida;
(b) pelo menos um tensoativo não iônico da fórmula I
R1-O-(AO)x-(H) (I)
em que
R1 representa alquila de cadeia reta ou ramificada tendo de 4 a
20 átomos de carbono;
AO é etilenoóxi, propilenoóxi ou uma mistura de etilenoóxi e
propilenoóxi e
χ corresponde aos valores de 2 a 20 e
(c) pelo menos um alcoilato de tristirilfenila iônico e (d) pelo menos um óleo e
(e) água,
em que o pesticida está presente na fase aquosa na forma de uma suspensão e o óleo é essencialmente isento de pesticida.
A formulação também pode, opcionalmente, ainda compreender um solvente (f). A formulação também pode, opcionalmente, ainda compreender um tensoativo não iônico (g). A formulação também pode, opcionalmente, ainda compreender formulações auxiliares adicionais (h).
Preferivelmente, as quantidades respectivas de componentes
(a) a (f) são como segue: A quantidade do pelo menos um pesticida (a) é de 1 % até 60 % em peso; preferivelmente 5 a 50, mais preferivelmente 7,5 a 30 % em peso. A quantidade de tensoativo não iônico (b) da fórmula I é de 0,5 % até 30 % em peso; preferivelmente 2 a 5 % em peso. A quantidade de etoxilado de tristirilfenila iônico (c) é de 0,5 % até 30 % em peso; preferivelmente 5 a 15 % em peso. A quantidade de óleo (d) é de 5 % até 50 % em peso; preferivelmente de 20 a 40 % em peso. Se um solvente (f) estiver presente, a quantidade de solvente será de 5 % até 50 % em peso preferivelmente 20 a 40 % em peso. Se um tensoativo não iônico (g) estiver presente na formulação, a quantidade de tensoativo não iônico selecionada do grupo consistindo de copolímeros em bloco de etilenoóxido / propileneóxido é de 0,5 % até 20 % em peso.
No geral, a quantidade de água (e) adiciona até 100 % em peso.
Se as formulações auxiliares adicionais estiverem presentes, a quantidade de formulações auxiliares adicionais será de 0,1 % até 2 % em peso preferivelmente 0,5 a 1 % em peso.
Os compostos da fórmula I são bem conhecidos na técnica e descritos, por exemplo, inter alia em WO 03/00053, WO 00/35278, WO
05/105285 e EP 1 140 741.
Que a combinação específica de compostos da fórmula I com pelo menos um alcoxilato de tristirilfenila iônico representa um sistema favorável para formulações agroquímicas com base em água líquida não divulgado em qualquer um destes documentos.
Além disso, etilenoóxi, que representa -CH2-CH2-O- é abreviado a seguir como "EO" e propilenoóxi, que representa -CH2"CH(CH3)- O- é abreviado a seguir como "PO". Na fórmula I, m e η representa valores médios.
Um grupo preferido de tensoativo não iônicos são alcoxilados
de álcool da fórmula Ia
R1-0-(-A0-)0-H (Ia)
em que R1 tem o significado indicado acima: e o representa números de 2 a 20.
Um outro grupo preferido de tensoativos não iônicos são alcoxilados de álcool da fórmula Ib
R1 -0-(-E0-)n-(-P0-)m-H (Ib)
em que
R1 tem o significado indicado acima e m representa números de 1 a 10 e η representa números de 1 a 10.
Um outro grupo preferido de tensoativos não iônicos são alcoxilados de álcool da fórmula Ic
R1-(X-PO)r-(EO)s-H (Ic)
em que
R1 tem o significado indicado acima, r representa números de 1 a 10 e s representa números de 1 a 10.
Um outro grupo preferido de tensoativo não iônicos são alcoxilados de álcool da fórmula Id
CH3(CH2)tCH2O (CH2CH2O)u-H (Id) em que
t representa números de 8 a 13 e u representa números de 6 a 17.
Nas fórmulas indicadas anteriormente R1 preferivelmente representa butila, i-butila, n-pentila, i-pentila, neopentila, n-hexila, i-hexila, n- octila, i-octila, 2-etil-hexila, nonila, i-nonila, decila, n-dodecila, i-dodecila, laurila, miristila, i-tridecila, trimetil-nonila, palnitila, estearila ou eicosila, em que 2 etil-hexila é preferido.
Preferidos são os tensoativos não iônicos são alcoxilados de álcool da fórmula Ib e Ic, em que R1 é 2-etil-hexila [CH3-CH2-CH2-CH2- CH(C2H5)-CH2-].
Mais preferidos são alcoxilados de álcool da fórmula Ib-1, em
que
CH3-CH2-CH2-CH2-CH(C2H5)-CH2-(EO)n-(PO)m (Ib-1) m é 1 a 5 e
η é 1 a 5;
em que η é preferivelmente 3 a 5, m é preferivelmente a um valor de 1 a 2 e alcoxilados de álcool da fórmula Ic-1
CH3-CH2-CH2-CH2-CH(C2H5)-CH2-(-PO-)r-(EO-)s-H (Ic-1) rélalO, preferivelmente 6 e
s é 1 a 10, preferivelmente 8 e alcoxilados de álcool da
fórmula Ic-2
CH3-CH2-CH2-CH2-CH(C2H5)-CH2-(-PO-)r-(EO-)s-H (Ic-2) r é 1 a 5, preferivelmente 1 a 3 e s é 1 a 5, preferivelmente 2 a 4
Os mais preferidos são alcoxilados de álcool da fórmula Ib, em que alcoxilados de álcool da fórmula Ib-I são mais preferidos.
Como mencionado acima, em todos os alcoxilados de álcool da fórmula I, os números dados para m, n, o, r, s e u são valores médios (valores médios).
Além disso, as fórmulas acima dão uma definição geral dos alcoxilados de álcool. Estas substâncias são misturas de substâncias do tipo indicado tendo comprimentos de cadeia diferentes. Para os índices, portanto, os valores médios são calculados também podendo ser diferentes para números inteiros.
Por meio de exemplo, um alcoxilado de álcool da fórmula (Ic- 1) pode ser mencionado, em que r representa o valor médio 6,2 e s representa o valor médio 8,3.
Os alcoxilados de tristirilfenila iônicos (c) são, preferivelmente, fosfatados ou sulfatados e, opcionalmente neutralizados por uma base. Mais preferivelmente, os alcoxilados de tristirilfenila compreendem a fórmula II
em que w é 3 e
ν é 1 a 60, mais preferivelmente 10 a 25 e mais
preferivelmente 16,[ AO é EO, PO ou uma mistura de EO e porção PO preferivelmente EO e
R2 é SO3H ou H2PO3.
As formas de ácido livre respectivas da fórmula II também podem ser neutralizadas com uma base, por exemplo, um hidróxido de metal alcalino (por exemplo, NaOH, KOH) ou amoníaco ou uma amina (por exemplo, da fórmula III
NR1R2R3 (III)
12 3
em que R', Rz e Rj são, independentemente um do outro,
• 12 3·
hidrogênio metila, etila ou propila, preferivelmente R , R e R são etila) em
___
solução aquosa resultando em Rz = SO3X ou HPO3Y (em que XeY representam, independentemente um do outro NH4+, (NR1R2R3)+ com R1, R2 e R3 como definido acima, Na+ ou K+.
Os mais preferidos são etoxilados de tristirilfenol iônicos, que são, preferivelmente fosfatados ou sulfatados e, opcionalmente neutralizados por uma base, mais preferivelmente aqueles em que R é SO3X e HPO3Y, em que XeY tem o significado como definido acima. Aqui, os etoxilados de tristirilfenil da fórmula IIa são mais preferidos: (IIa) em que ν é 1 a 60, mais preferivelmente 10 a 25 e mais preferivelmente 14 a 18 e
R2 é SO3H ou H2PO3
As formas de ácido livre respectivas também podem ser neutralizadas com uma base, por exemplo, um hidróxido de metal alcalino (por exemplo, NaOH, KOH) ou amoníaco ou uma amina (por exemplo da fórmula III
NR1R2R3 (III)
em que R1, R2 e R3 são, independentemente, um do outro,
12 3 ·
hidrogênio, metila, etila ou propila, preferivelmente R5ReR são etila) em solução aquosa resultando em R2 = SO3X ou HPO3Y (em que XeY
+ ι 2 3+ 12
representam, independentemente um do outro NH4 , (NR RR) com R1, R e R3 como definido acima ou K+.
Os mais preferidos são compostos da fórmula IIa, em que R é SO3X e HPO3Y, em que XeY tem o significado como definido acima.
A preparação de compostos da fórmula II e IIa é conhecida na técnica e pode ser realizada, por exemplo, em analogia com os métodos descritos na US 5.082.591. Os compostos da fórmula II e IIa podem ser obtidos por condensação de estireno em fenol seguido por etoxilação ou por etoxilação-propoxilação. alcoxilato de tristirilfenila aniônicos podem ser preparados por fosfatação (por exemplo com P2O5) ou Sulfatação (por exemplo com H2NSO3H) opcionalmente seguido pela neutralização com uma base (por exemplo hidróxido alcalino ou amoníaco) os compostos da fórmula I e/ou II estão disponíveis em produtos comerciais, por exemplo, Soprofor FLK, Soprohor FL, Soprofor 4D384, Soprofor 4D360 (sal de potássio, sal de trietanolamina, sal de NH4+) da Rhodia.
O termo "pelo menos um óleo" (d) significa que um óleo ou uma mistura de óleos pode ser usada.
O óleo (d) pode ser selecionado do grupo consistindo de óleos
minerais e óleos sintéticos e óleos vegetais (planta) e animais, por exemplo, misturas de ácidos graxos Cg a C22- Os exemplos são frações de óleo mineral de ponto de ebulição de médio a alto, por exemplo, querosene e combustível diesel, derivados de petróleo, além de óleos de alcatrão, hidrocarbonetos, óleos de parafina, compostos não hidrogenados, hidrogenados ou parcialmente hidrogenados aromáticos ou alquilaromáticos das séries de benzeno ou naftaleno, gorduras e óleos de origem vegetal ou animal, tais como mono-, di- e triglicerídeos puros ou como uma mistura, por exemplo, na forma de extratos oleosos de produtos naturais, por exemplo, óleo de oliva, óleo de soja, óleo de girassol, óleo de mamona, óleo de gergelim, óleo de milho, óleo de amendoim, óleo de semente de colza, óleo de semente de linhaça, óleo de amêndoa, óleo de girassol, coco, semente de palma, palma, soja, semente de colza, canola, milho, mas também óleo de sebo, óleo de esperma, óleo de arenque, óleo de mamona e seus rafinatos, por exemplo, produtos hidrogenados ou parcialmente hidrogenados destes, em particular ésteres metílicos e etílicos. Os óleos preferidos são qualquer tipo de óleo mineral (derivados de petróleo) mas também óleos vegetais como, semente de palma, palma, soja, semente de colza, canola, milho, mas também óleo de sebo, óleo de esperma, óleo de arenque, óleo de mamona, que são misturas de ácidos graxos C8 a C22 de ocorrência natural e que podem ser produtos opcionalmente hidrogenados ou parcialmente hidrogenados destes, em particular ésteres etílicos.
O termo "pelo menos um solvente" (f) significa que um solvente orgânico ou uma mistura de solventes orgânicos podem ser usados. O solvente orgânico (f) pode ser um solvente polar ou não polar. Os exemplos de solventes adequados (f) são derivados de petróleo aromáticos de C8 a Cn (hidrocarbonetos aromáticos) com uma solubilidade em água < 0,1 % (p/p) e uma faixa de diluição de 130° C a 300° C (comercialmente disponíveis sob os seguintes nomes comerciais: Solvesso 100, Solvesso 150, Solvesso 200, Solvesso 150ND, solvesso 200ND, Aromatic 150, Aromatic 200, Hydrosol A 200, Hydrosol A 230/270, Caromax 20,Caromax 28, Aromat K 150, Aromat K 200, Shellsol A 150, Shellsol A 100, Fin FAS-TX 150, Fin FAS-TX 200), os hidrocarbonetos, tais como aromático esgotado, linear parafínico, isoparafínico, cicloparafínico tendo um ponto cintilante entre 40° C e 250° C e uma faixa de diluição de 150° C a 450° C, Anisol, sulfóxido de dimetila (DMSO), N-Metilvalerolactam e Lactonas, tais como γ-Butirolactona e ésteres, tais como acetato de benzila, benzoato de benzila, benzoato de butila, 2-, acetato de etoxipropila, metil proxitol acetato; fosfato de Tributila e Amidas, tais como N,N-dimetil octanamida e/ou Ν,Ν-dimetil decanamida e cetonas, tais como 2-heptanona, cicloexanona, acetofenona e derivados de acetofenona, tais como 4-metóxi acetofenona e álcoois, tais como cicloexanol, álcool benzílico diacetona álcool, por exemplo, 4-hidróxi-4-metil-2-pentanona, n-octanol, 2 etilhexanol Diésteres, tais como misturas de glutarato de dimetila, succinato de dimetila e adipato de dimetila ou misturas de glutarato de diisobutila, succinato de diisobutila e adipato de diisobutila e glicol e derivados, tais como polietileno glicol, glicerol, propileno glicol, propileno glicol acetato de éter monometílico, éter monometílico de dipropileno glicol, éter monofenílico de propileno glicol e carbonatos de alquileno, tais como carbonato de propileno, carbonato de butileno carbonato de butileno e derivados de pirrolidona, tais como N-octilpirrolidona, N-etil pirrolidona, N-docedil pirrolidona, e Lactato ésteres, tais como n-propil lactato, metil lactato, etil lactato, isopropil lactato, butil lactato, comercialmente disponíveis sob os nomes comerciais Purasolv NPL - Purasolv ML - Purasolv EL - Purasolv IPL Purasolv BL ou misturas selecionadas de pelo menos dois dos solventes mencionados acima.
Como mencionado acima, a formulação líquida compreende pelo menos um óleo (d) e ainda opcionalmente pelo menos um solvente (f).
O pesticida pode ser dissolvido em um óleo ou uma mistura de pelo menos um óleo e pelo menos um solvente (e depois emulsificado em água) ou dissolvido em água (se o pesticida for solúvel em água).
De acordo com a invenção o pesticida está presente na fase aquosa na forma de uma suspensão e o óleo é essencialmente isento de pesticida. O termo "essencialmente" significa a que concentração de pesticida no óleo não está excedendo 5 % em peso, preferivelmente 2 % em peso e especialmente 0,5 % em peso, com respeito ao peso total do óleo.
No caso que mais do que um pesticida é usado, por exemplo dois, os pesticidas podem estar presentes na forma sólida (suspensão em água) ou solubilizado em água. Aqui, os pesticidas podem estar presentes sob a mesma forma (por exemplo ambos estão presentes na forma sólida na forma de uma suspensão) ou sob formas diferentes (por exemplo um pesticida é solubilizado em água e o outro está presente na forma de uma suspensão na fase aquosa). em uma forma de realização preferida particular, ambos os pesticidas estão presentes na forma de uma suspensão na fase aquosa e o óleo é essencialmente isento de pesticida. Aqui, é preferido que a formulação não compreenda um solvente orgânico.
As formulações como definido acima, ainda podem compreender um tensoativo não iônico (g) selecionado do grupo de copolímeros em bloco de óxido de etileno propileno, em que o peso molecular de tais polímeros pode estar em uma faixa de 850 g/mol a 3250 g/mol (por exemplo comercialmente disponíveis como tipos Pluronic® PE da BASF (por exemplo Pluronic® PE 3100, Pluronic® PE 3500, Pluronic® PE 4300, Pluronic® PE 6100, Pluronic® PE 6200, Pluronic® PE 6400, Pluronic® PE 6800, Pluronic® PE 7400, Pluronic® PE 8100, Pluronic® PE 9200, Pluronic® PE 9400, Pluronic® PE 10100, Pluronic® PE 10300, Pluronic® PE 10400, Pluronic® PE 10500).
Em uma forma de realização preferida particular, a formulação
compreende
(a) um ou dois pesticidas presentes na forma de uma
suspensão;
(b) pelo menos um tensoativo não iônico da fórmula I, preferivelmente Ib ou Ic, mais preferivelmente Ib-I ou Ic-I ou Ic2, mais preferivelmente Ib-I
(c) pelo menos um alcoilato de tristirilfenila iônico, preferivelmente da fórmula II, mais preferivelmente da fórmula II, mais preferivelmente da fórmula IIa e
(d) pelo menos um óleo, em que o óleo é essencialmente isento
de pesticida e
(e) água e
(g) tensoativo não iônico (g) selecionado do grupo de copolímeros em bloco de óxido de etileno propileno e nenhum solvente.
Opcionalmente, a formulação também pode compreender formulações auxiliares adicionais (h) adequadas para a formulação de produtos agroquímicos, tais como tensoativos adicionais, agentes antiespumantes, agentes anti-congelantes, estabilizantes, conservantes e/ou antioxidantes opcionalmente se a formulação for pretendida para os propósitos de tratamento de semente, pigmentos e/ou aglutinantes.
Os estabilizantes adequados são, por exemplo, ácidos carboxílicos (ácido cítrico, ácido acético, ácido dodecilbenzenossulfônico), ácido ortofosórico, ácido dodecilbenzenossulfônico e seus sais adequados. Os antioxidantes adequados são, por exemplo, o butilidroxitolueno.
Os conservantes adequados são, por exemplo, 1,2- benzisotiazolin-3-ona e/ou 2-Metil-2H-isotiazol-3-ona ou benzoato de sódio ou ácido benzóico.
Os agentes anticongelamento adequados são, por exemplo, glicerina, etileno glicol, hexilenoglicol e propileno glicol.
Os agentes anti-espumantes adequados são, por exemplo,
agentes anti-espumantes com base em silício, por exemplo polidimetilsiloxanos.
O aglutinantes adequados podem ser adicionados para melhorar a adesão dos materiais ativos nas sementes após o tratamento. Os aglutinantes adequados são polivinilpirrolidona, Polivinilacetato, polivinilálcool e tilose.
Os pigmentos adequados para o tratamento de formulações de semente são Rhodamin B, C.I. Pigment red 112, C.I. Solvent red 1, pigment blue 15:4, pigment blue 15:3, pigment blue 15:2, pigment blue 15:1, pigment blue 80, pigment yellow 1, pigment yellow 13, pigment red 112, pigment red 48:2, pigment red 48:1, pigment red 57:1, pigment red 53:1, pigment orange 43, pigment orange 34, pigment orange 5, pigment green 36, pigment green 7, pigment white 6, pigment brown 25, basic violet 10, basic violet 49, acid red 51, acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108. Estes devem ser solúveis em solventes.
As formulações são preparadas de uma maneira conhecida (ver, por exemplo, para revisão US 3,060,084, EP-A 707 445 (para concentrados líquidos), Chemical Engineering, Dec. 4, 1967, 147-48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York, 1963, páginas 8-57 e et seq. WO 91/13546, US 4,172,714, US 4,144,050, US 3,920,442, US 5,180,587, US 5,232,701, US 5,208,030, GB 2,095,558, US 3,299,566, Klingman, Weed Control as a Science, John Wiley and Sons, Inc., New York, 1961, Hance et al., Weed Control Handbook, 8th Ed., Blackwell Scientific Publications, Oxford, 1989 and Mollet, H., Grubemann, Α., Formulation technology, Wiley VCH Verlag GmbH, Weinheim (Germany), 2001, 2. D. A. Knowles, Chemistri and Technology of Agrochemical Formulations, Kluwer Academic Publishers, Dordrecht, 1998 (ISBN 0-7514-0443-8), por exemplo, estendendo-se o pesticida com o solvente e/ou óleo mineral como definido acima e tensoativos (b), (c) e, opcionalmente (f) de acordo com a presente invenção como definido acima e ainda, opcionalmente tensoativos e auxiliares de formulação como definido acima.
Por exemplo, as formulações podem ser preparadas, fragmentando-se os pesticida com a adição de óleo, solvente como definido acima sob agitação até o ativo estar totalmente na solução, depois pela adição (agentes emulsifícadores, anti-congelamento, anti-espumantes e ultimamente água) e, se apropriado, ainda auxiliares como conservantes de pigmento em um recipiente. Um outro exemplo para preparação é preparar uma pré-mistura com base em trituração úmida dos pesticidas / para ajustar com a distribuição de tamanho de partícula requerido. A esta base de trituração úmida, as formulações auxiliares adicionais são adicionadas, tal como, por exemplo, anti-espumas e espessante. Um óleo e opcionalmente um emulsificante são misturados e agitados para a preparação de uma solução oleosa. A base de trituração úmida com os auxiliares de formulação (anti-espumas e espessante) é misturada sob agitação com a solução oleosa para dar a formulação final.
O termo "pelo menos um pesticida" dentro do significado dos estabelecidos dentro da técnica, a invenção estabelece que um ou mais compostos podem ser selecionados do grupo que consiste de fungicidas, inseticidas, herbicidas nematicidas e/ou protetor ou reguladores de desenvolvimento podem ser usados. O técnico habilitado é familiar com tais pesticidas, que pode ser, por exemplo, observado no pesticida Manual, 13° Ed. (2003), The British Crop Protection Council, London.
A seguinte lista de pesticidas junto com os quais os compostos de acordo com a invenção pode ser usada, é pretendida para ilustrar as possibilidades, mas não impõe qualquer limitação:
O inseticida pode ser selecionado do grupo consistindo de A.l. Organo(tio)fosfatos: acefato, azametifos, azinfos-metila, clorpirifos, clorpirifos-metila, clorfenvinfos, diazinon, diclorvos, dicrotofos, dimetoato, disulfoton, etion, fenitrotion, fention, isoxation, malation, metamidofos, metidation, metil-paration, mevinfos, monocrotofos, oxidemeton-metila, paraoxon, paration, fentoato, fosalone, fosmet, fosfamidon, forato, foxim, pirimifos-metila, profenofos, protiofos, sulprofos, tetraclorvinfos, terbufos, triazofos, triclorfon;
A.2. Carbamatos: alanicarb, aldicarb, bendiocarb, benfuracarb, carbarila, carbofuran, carbosulfan, fenoxicarb, furatiocarb, metiocarb, metomila, oxamila, pirimicarb, propoxur, tiodicarb, triazamato;
A.3. Piretróides: aletrin, bifentrin, ciflutrin, cialotrin, cifenotrin, cipermetrin, alfa-cipermetrin, beta-cipermetrin, zeta-cipermetrin, deltametrin, esfenvalerato, etofenprox, fenpropatrin, fenvalerato, imiprotrin, lambda-cialotrin, gamma-cialotrin, permetrin, praletrin, piretrin I e II, resmetrin, silafluofen, tau-fluvalinato, teflutrin, tetrametrin, tralometrin, transflutrin, proflutrin, dimeflutrin; A.4. Reguladores de desenvolvimento: a) inibidores da síntese
de quitina: benzoiluréias: clorfluazuron, diflubenzuron, flucicloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, teflubenzuron, triflumuron; buprofezin, diofenolan, hexitiazox, etoxazol, clofentazina; b) antagonistas de ecdisona: halofenozida, metoxifenozida, tebufenozida, azadiractina; c) juvenóides: piriproxifen, metopreno, fenoxicarb; d) inibidores da biossíntese de lipídeo: espirodiclofen, espiromesifen, espirotetramat;
A.5. compostos agonistas/antagonistas receptores de nicotina: clotianidin, dinotefiiran, imidacloprid, tiametoxam, nitenpiram, acetamiprid, tiacloprid; O composto de tiazol da fórmula (Γ1)
-N,
10
Cl
Γ "Ί
Vn-
NO,
(Γ1)
A.6. compostos antagonistas de GABA: acetoprol, endosulfan, etiprol, fipronila, vaniliprol, pirafluprol, piriprol, o composto de fenilpirazol da fórmula Γ2
O S
Il
CF-
H2N ν
NH„
Cl
Cl
(P)
CF,
A. 7. Inseticidas de lactona macrocíclicos: abamectin, emamectin, milbemectin, lepimectin, spinosad e composto da fórmula (Γ3) (CAS No. 187166-40-1)
Me 2 N.,
(Γ3),
A.8. compostos METI I: fenazaquin, piridaben, tebufenpirad, tolfenpirad, flufenerim;
A.9. compostos METI II e III: acequinocila, fluaciprim,
hidrametilnon;
A. 10. Compostos não ligadores: clorfenapir; Α. 11. compostos inibidores de fosforilação oxidativa: ciexatin, diafentiuron, oxido de fenbutatin, propargita;
A. 12. compostos interruptores de mudança: ciromazina;
A. 13. compostos inibidores da oxidase de função mista: butóxido de piperonila;
A. 14. compostos bloqueadores do canal de sódio: indoxacarb, metaflumizona,
A. 15. Vários: benclotiaz, bifenazato, cartap, flonicamid, piridalila, pimetrozine, enxofre, tiociclam, flubendiamida, cienopirafen, flupirazofos, ciflumetofen, amidoflumet, o composto de aminoquinazolinona da fórmula Γ
di(R'' ')propionamido-2-(2,6-dicloro- a,a,a,-trifluoro-p-tolil)-hidrazona, em que R' é metila ou etila, halo é cloro ou bromo, R" é hidrogênio ou metila e R"' é metila ou etila, compostos de antranilamida da fórmula Γ5
Cl ou Br, I" é H, F, Cl, CF3, B1 é hidrogênio, Cl, Br, I, CN, B2 é Cl, Br, CF3, OCH2CF3, OCF2H, e Rb é hidrogênio, CH3 ou CH(CH3)2 e compostos de malonitrila como descrito em JP 2002 284608, WO 02/89579, WO 02/90320,
N-R'-2,2-
Y"
em que A1 é CH3, Cl, Br, I, X é C-H, C-Cl, C-F ou Ν, Γ é F, WO 02/90321, WO 04/06677, WO 04/20399, JP 2004 99597, WO 05/68423, WO 05/68432 ou WO 05/63694, especialmente os compostos de malonitrila CF3(CH2)2C(Cn)2CH2(CF2)3CF2H, CF3(CH2)2C(Cn)2CH2(CF2)5CF2H,
CF3(CH2)2C(CN)2(CH2)2C(CF3)2F, CF3(CH2)2C(Cn)2(CH2)2(CF2)3CF3, Cf2H(CF2)3CH2C(CN)2CH2(CF2)3CF2H, CF3(CH2)2C(Cn)2CH2(CF2)3CF3, Cf3(CF2)2CH2C(CN)2CH2(CF2)3CF2H, e Cf3CF2CH2C(CN)2CH2(CF2)3CF2H Os compostos comercialmente disponíveis do grupo A podem ser encontrados em The Pesticide Manual, 13° Edition, British Crop Protection Council (2003) entre outras publicações. As Tioamidas da fórmula Γ2 e sua preparação foram descritas no WO 98/28279. Lepimectina é conhecida da Agro Project, PJB Publications Ltd, November 2004. Benclotiaz e sua preparação foi descrita no EP-Al 454621. Metidation e Paraoxon e sua preparação foram descritos em Farm Chemicals Handbook, Volume 88, Meister Publishing Company, 2001. Acetoprol e sua preparação foram descritos em WO 98/28277. Metaflumizona e sua preparação foram descritos em EP-Al 462 456. Flupirazofos foram descritos em Pesticide Science 54, 1988, p.237-243 e no US 4822779. Pirafluprol e sua preparação foram descritos em JP 2002193709 e em WO 01/00614. Piriprol e sua preparação foram descritos no WO 98/45274 e em US 6335357. Amidoflumet e sua preparação foram descritos em US 6221890 e em JP 21010907. Flufenerim e sua preparação foram descritos em WO 03/007717 e em WO 03/007718. Ciflumetofen e sua preparação foram descritos em WO 04/080180. As Antranilamidas da fórmula Γ5 e sua preparação foram descritas em WO 01/70671; WO 02/48137; WO 03/24222, WO 03/15518, WO 04/67528; WO 04/33468 e WO 05/118552. Os compostos de malonitrila CF3(CH2)2C(Cn)2CH2(CF2)3CF2H, CF3(CH2)2C(Cn)2CH2(CF2)5CF2H,
CF3(CH2)2C(CN)2(CH2)2C(CF3)2F, CF3(CH2)2C(Cn)2(CH2)2(CF2)3CF3, Cf2H(CF2)3CH2C(CN)2CH2(CF2)3CF2H, CF3(CH2)2C(Cn)2CH2(CF2)3CF3, Cf3(CF2)2CH2C(CN)2CH2(CF2)3CF2H, e Cf3CF2CH2C(CN)2CH2(CF2)3CF2H foram descritos em WO 05/63694.
O fungicida pode ser selecionado do grupo consistindo de
1. Estrobilurinas, tais como azoxistrobin, dimoxistrobin, enestroburin, fluoxastrobin, cresoxim-metila, metominostrobin, picoxistrobin,
piraclostrobin, trifloxistrobin, orisastrobin, (2-cloro-5-[l-(3- metilbenziloxiimino)etil]benzil)carbamato de metila, (2-cloro-5-[l-(6-metil- piridin-2-ilmetoxiimino)etil]benzil)carbamato de metila, 2-(orto-((2,5-dimetil- feniloximetileno)fenil)-3-metoxiacrilato de metila;
2. Carboxamidas, tais como
carboxanilidas: benalaxila, benodanila, boscalid, carboxin,
mepronila, fenfuram, fenhexamid, flutolanila, furametpir, metalaxila, ofurace, oxadixila, oxicarboxin, pentiopirad, tifluzamida, tiadinila, N-(4’- bromobifenil-2-il)-4-difluorometil-2-metiltiazol-5-carboxamida, N-(4’-
trifluorometilbifenil-2-il)-4-difluorometil-2-metiltiazol-5-carboxamida, N-(4’-
cloro-3 ’-fluorobifenil-2-il)-4-difluorometil-2-metiltiazol-5-carboxamida, N- (3 ’ ,4’ -dicloro-4-fluorobifenil-2-il)-3 -difluorometil-1 -metilpirazol-4- carboxamida, N-(2-cyanofenil)-3,4-dicloroisotiazol-5-carboxamida;
morfolidas de ácido carboxílico: dimetomorph, flumorph; benzamidas: flumetover, fluopicolida (picobenzamid),
zoxamida;
outras carboxamidas: carpropamid, diclocimet, mandipropamid, N-(2-(4-[3-(4-clorofenil)prop-2-inilóxi]-3-metoxifenil)etil)- 2-metano-sulfonilamino-3-metilbutiramida, N-(2-(4-[3-(4-clorofenil)prop-2- inilóxi]-3-metoxifenil)etil)-2-etanesulfonilamino-3-metilbutiramida;
3. Azóis, tais como
triazóis: bitertanol, bromuconazol, ciproconazol, difenoconazol, diniconazol, enilconazol, epoxiconazol, fenbuconazol, flusilazol, fluquinconazol, flutriafol, hexaconazol, imibenconazol, ipconazol, metconazol, miclobutanila, penconazol, propiconazol, protioconazol, simeconazol, tebuconazol, tetraconazol, triadimenol, triadimefon, triticonazol;
imidazóis: ciazofamid, imazalila, pefurazoato, procloraz,
triflumizol;
benzimidazóis: benomila, carbendazim, fuberidazol,
tiabendazol;
outros: etaboxam, etridiazol, himexazol;
4. compostos de heterociclila nitrogenosos, tais como piridinas: fluazinam, pirifenox, 3-[5-(4-clorofenil)-2,3-
dimetilisoxazolidin-3 -il]-piridina;
pirimidinas: bupirimato, ciprodinila, ferimzona, fenarimol,
mepanipirim, nuarimol, pirimetanil;
piperazinas: triforina; pirróis: fludioxonila, fenpiclonil;
morfolinas: aldimorph, dodemorph, fenpropimorph,
tridemorph;
dicarboximidas: iprodione, procimidone, vinclozolin; outros: acibenzolar-S-metila, anilazina, captan, captafol, dazomet, diclomezina, fenoxanila, folpet, fenpropidin, famoxadona, fenamidona, octilinona, probenazol, proquinazid, piroquilon, quinoxifen, 20 triciclazol, 5-cloro-7-(4-metilpiperidin-l-il)-6-(2,4,6-trifluorofenil)-[l,2,4]tri- azolo[l,5-a]pirimidina, 2-butóxi-6-iodo-3-propilcromen-4-ona, N,N-dimetil- 3 -(3-bromo-6-fluoro-2-metilindol-1 -sulfonil)-[ 1,2,4]triazol-1 -sulfonamida;
5. Carbamatos e ditiocarbamatos, tais como ditiocarbamatos: ferbam, mancozeb, maneb, metiram, metam,
propineb, tiram, zineb, ziram;
Carbamatos: dietofencarb, flubentiavalicarb, iprovalicarb, propamocarb, 3-(4-clorofenil)-3-(2-isopropoxicarbonilamino-3-
metilbutirilamino)-propionato de metila, N-(l-(l-(4-
cianofenil)etanesulfonil)but-2-il)carbamato de 4-fluorofenila; 6. Outros fungicidas, tais como guanidinas: dodina, iminoctadina, guazatina; antibióticos: kasugamicina, polioxinas, estreptomicina, validamicina A;
compostos organometálicos: sais de fentina;
compostos de heerociclila contendo enxofre: isoprotiolano,
ditianon;
compostos de organofósforo: edifenfos, fosetila, fosetil- alumínio, iprobenfos, pirazofos, tolclofos-metila, ácido fosforoso e seus sais;
compostos de organocloro: tiofanato-metila, clorotalonila, diclofluanid, tolilfluanid, flusulfamida, ftalida, hexaclorbenzeno, pencicuron, quintozeno;
derivados de nitrofenila: binapacrila, dinocap, dinobuton; compsotos ativos inorgânicos: mistura de Bordeaux, acetato de cobre, hidróxido de cobre, oxicloreto de cobre, sulfato de cobre básico, enxofre;
outros: espiroxamina, ciflufenamid, cimoxanila, metrafenona. O herbicida é selecionado do grupo consistindo de bl) Inibidores da biossíntese de lipídeo, tais como clorazifop, clodinafop, clofop, cihalofop, diclofop, fenoxaprop, fenoxaprop-p, fentiaprop, fluazifop, fluazifop-P, haloxifop, haloxifop-P, isoxapirifop, metamifop, propaquizafop, quizalofop, quizalofop-P, trifop, alloxidim, butroxidim, cletodim, cloproxidim, cicloxidim, profoxidim, setoxidim, tepraloxidim, tralcoxidim, butilato, cicloato, dialato, dimepiperato, EPTC, esprocarb, etiolato, isopolinato, metiobencarb, molinato, orbencarb, pebulato, prosulfocarb, sulfalato, tiobencarb, tiocarbazila, trialato, vemolato, benfuresato, etofumesato e bensulida;
b2) inibidores de ALS, tais como amidosulfuron, azimsulfuron, bensulfuron, clorimuron, clorsulfuron, cinosulfuron, ciclosulfamuron, etametsulfuron, etoxisulfuron, flazasulfliron, flupirsulfuron, foramsulfiiron, halosulfuron, imazosulfiiron, iodosulfuron, mesosulfuron, metsulfuron, nicosulfüron, oxasulfuron, primisulfuron, prosulfuron, pirazosulfuron, rimsulfuron, sulfometuron, sulfosulfuron, tifensulfuron, 5 triasulfuron, tribenuron, trifloxisulfuron, triflusulfuron, tritosulfuron, imazametabenz, imazamox, imazapic, imazapir, imazaquin, imazetapir, cloransulam, diclosulam, florasulam, flumetsulam, metosulam, penoxsulam, bispiribac, piriminobac, propoxicarbazona, flucarbazona, piribenzoxim, piriftalid e piritiobac;
b3) inibidores de fotossíntese, tais como atraton, atrazina,
ametrina, aziprotrine, cianazine, cianatrin, clorazina, ciprazina, desmetrina, dimetametrina, dipropetrin, eglinazina, ipazina, mesoprazina, metometon, metoprotrina, prociazina, proglinazina, prometon, prometrina, propazina, sebutilazina, secbumeton, simazina, simeton, simetrina, terbumeton, 15 terbutilazina, terbutrina, trietazina, ametridione, amibuzin, hexazinone, isometiozin, metamitron, metribuzin, bromacila, isocila, lenacila, terbacila, brompirazon, cloridazon, dimidazon, desmedifam, fenisofam, fenmedifam, fenmedifam-etila, benztiazuron, butiuron, etidimuron, isouron, metabenztiazuron, monoisouron, tebutiuron, tiazafluron, anisuron, buturon, 20 clorbromuron, cloreturon, clorotoluron, cloroxuron, difenoxuron, dimefuron, diuron, fenuron, fluometuron, fluotiuron, isoproturon, linuron, metiuron, metobenzuron, metobromuron, metoxuron, monolinuron, monuron, neburon, parafluron, fenobenzuron, siduron, tetrafluron, tidiazuron, ciperquat, dietamquat, difenzoquat, diquat, morfamquat, paraquat, bromobonila, 25 bromoxinila, cloroxinila, iodobonila, ioxinila, amicarbazona, bromofenoxim, flumezin, metazol, bentazone, propanila, pentanoclor, piridato, and piridafol;
b4) inibidores da protoporfirinogeno-IX oxidase, tais como acifluorfen, bifenox, clometoxifen, clomitrofen, etoxifen, fluorodifen, fluoroglicofen, fluoronitrofen, fomesafen, furiloxifen, halosafen, lactofen, nitrofen, nitrofluorfen, oxifluorfen, fluazolato, piraflufen, cinidon-etila, flumiclorac, flumioxazin, flumipropin, flutiacet, tidiazimin, oxadiazon, oxadiargila, azafenidin, carfentrazona, sulfentrazona, pentoxazona, benzfendizona, butafenacila, piraclonila, profluazol, flufenpir, flupropacila, nipiraclofen e etnipromid;
b5) herbicidas alvejantes, tais como metflurazon, norflurazon, flufenican, diflufenican, picolinafen, beflubutamid, fluridona, flurocloridona, flurtamona, mesotriona, sulcotriona, isoxaclortol, isoxaflutol, benzofenap, pirazolinato, pirazoxifen, benzobiciclon, amitrol, clomazona, aclonifen, 4-(3- trifluorometilfenoxi)-2-(4-trifluorometilfenil)pirimidina e também derivados de benzoíla substituídos por 3-heterociclila da fórmula II (ver em WO 96/26202, WO 97/41116, WO 97/41117 e WO 97/41118)
O ι-j
em que as variáveis RaR são como definidas abaixo:
R8, R10 são hidrogênio, halógeno, alquila Cj-C6, haloalquila Ci-C6, alcóxi CrC6, haloalcóxi CrC6, alquiltio CrC6, alquila CrC6 sulfinila ou alquila CrC6 sulfonila;
R9 é um radical heterocíclico selecionada do grupo consistindo de, tal como tiazol-2-ila, tiazol-4-ila, tiazol-5-ila, isoxazol-3-ila, isoxazol-4- ila, isoxazol-5-ila, 4,5-dihydroisoxazol-3-ila, 4,5-dihydroisoxazol-4-ila e 4,5- diidroisoxazol-5-ila, onde os nove radicais mencionados podem ser não substituídos ou mono- ou poli-substituído, por exemplo, mono-, di-, tri- ou tetra-substituído, por halógeno, alquila CrC4, alcóxi Ci-C4, haloalquila CpC4, haloalcóxi CrC4 ou alquiltio Cj-C4;
Ru é hidrogênio, halógeno ou alquila CrC6;
R12 é alquila CrC6;
13
R é hidrogênio ou alquila CrC6. b6) inibidores da EPSP sintase, tal como glifosato;
b7) inibidores da glutamina sintase, tais como glufosinato e
bilanafos;
b8) inibifores da DHP sintase, tal como asulam;
b9) inibidores da mitose, tais como benfluralin, butralin,
dinitramina, etalfluralin, flucloralin, isopropalin, metalpropalin, nitralin, orizalin, pendimetalin, prodiamina, profluralin, trifluralin, amiprofos-metila, butamifos, ditiopir, tiazopir, propizamida, tebutam, clortal, carbetamida, clorbufam, clorprofam e profam;
blO) inibidores de VLCFA, tais como acetoclor, alaclor,
butaclor, butenaclor, delaclor, dietatila, dimetaclor, dimetenamid, dimetenamid-P, metazaclor, metolaclor, S-metolaclor, pretilaclor, propaclor, propisoclor, prynaclor, terbuclor, tenilclor, xilaclor, alidoclor, CDEA, epronaz, difenamid, napropamida, naproanilide, petoxamid, flufenacet, 15 mefenacet, fentrazamida, anilofos, piperofos, cafenstrol, indanofan and tridifane;
bll) inibidores da síntese de celulose, tais como diclobenila, clortiamid, isoxaben e flupoxam;
b 12) herbicidas desligadores, tais como dinofenato, dinoprop, dinosam, dinoseb, dinoterb, DNOC, etinofen e medinoterb;
bl3) herbicidas de auxina, tais como clomeprop, 2,4-D, 2,4,5- T, MCPA, MCPA tioetila, diclorprop, diclorprop-P, mecoprop, mecoprop-P, 2,4-DB, MCPB, cloramben, dicamba, 2,3,6-TBA, tricamba, quinclorac, quinmerac, clopiralid, fluroxipir, picloram, triclopir e benazolin;
bl4) inibidores do transporte de auxina, tais como naptalam,
diflufenzopir;
bl5) benzoilprop, flamprop, flamprop-M, bromobutida, clorflurenol, cinmetilin, metildimron, etobenzanid, fosamina, metam, piributicarb, oxaziclomefona, dazomet, triaziflam e brometo de metila. Fungicidas e Inseticidas são preferidos.
Os intesiticas preferidos são
Carbamatos, tais como Alanicarb, Benfuracarb, Carbarila, Carbosulfan, Fenoxicarb, Furatiocarb, Indoxacarb, Metiocarb, Metomila, Oxamila, Pirimicarb, Propoxur, Tiodicarb, Triazamato;
Piretróides, tais como Bifentrin, Ciflutrin, Cipermetrin, alfa- Cipermetrin, Deltametrin, Esfenvalerato, Etofenprox, Fenpropatrin, Fenvalerato, Cihalotrin, Lambda-Cialotrin, Permetrin, Silafluofen, Tau- Fluvalinato, Teflutrin, Tralometrin, Zeta-Cipermetrin;
Reguladores do desenvolvimento de artrópodes, tais como
Inibidores da síntese de quitina: benzoiluréias: Clorfluazuron, Diflubenzuron, Flucicloxuron, Flufenoxuron, Hexaflumuron, Lufenuron, Novaluron, Teflubenzuron, Triflumuron; Buprofezin, Diofenolan, Hexitiazox, Etoxazol, Clofentazina;
b) antagonistas de ecdisona antagonists: Halofenozida,
Metoxifenozida, Tebufenozida;
c) juvenóides: Piriproxifen, Metopreno, Fenoxicarb;
d) inibidores da biossíntese de lipídeo: Espirodiclofen;
Neonicotinóides, tais como Acetamiprid, Clotianidin,
Flonicamid, Imidacloprid, Nitenpiram, Tiacloprid, Tiametoxam, Dinetofuran
e Etiprol, Fipronila, Metaflumizona, N-R’-2,2-dihalo-l- R,,ciclo-propanecarboxamida-2-(2,6-dicloro-a,a,a-tri-fluoro-p- tolil)hidrazona ou N-R’-2,2-di(R’ ’ ’)propionamida-2-(2,6-dicloro-a,a,a- trifluoro-p-tolil)-hidrazona, em que R’ é metila ou etila, halo é cloro ou
bromo, R” é hidrogênio ou metila e R’” é metila ou etila, Abamectin, Acequinocila, Amitraz, Azadirachtin, Bifenazato, Bacillus thuringiensis, Bacillus subtilis, Cartap, Clorfenapir, Clordimeform, Ciromazina, Diafentiuron, Diofenolan, Emamectin, Endosulfan, Fenazaquin, Formetanato, cloridreto de Formetanato, Hidrameti lnon, Indoxacarb, 4-{ (2Ζ)-2-( {[4-(trifluoro-metoxi)anilino]carbonil} hidrazono)- 2-[3-(trifluorometil)fenil]etil}benzo-nitrila, Piridaben, Piridalila, Pimetrozina, Spinosad, enxofre, Tebufenpirad e Tiociclam.
Os inseticidas mais preferidos são Fipronila, Flufenoxuron, Teflubenzuron, metaflumizona e Alfacipermetrin.
Os inseticidas mais preferidos são Fipronila, Flufenoxuron e Alfacipermetrin.
Como mencionado acima, também, as misturas de ativos são preferidas. Por exemplo, o inseticida que segue as misturas são preferidos: a mistura de alfacipermetrin e acetamiprid; a mistura de fipronil e imidacloprid; a mistura de fipronil e acetamiprid; a mistura de fiponil e acefato; a mistura de fipronila e tiametoxan; a mistura de fipronila e pimetrozina; a mistura de fipronil e alfacipermetrin; a mistura de metaflumizona e acetamiprid; a mistura de metaflumizona e teflubenzuron; a mistura de alfacipermetrin e clorpirifos e a mistura de metaflumizona e flufenoxuron, em que a mistura de fipronil e alfacipermetrin é mais preferida.
Os fungicidas preferidos são epoxiconazol, piraclostrobin, cresoxim-metila, carbendazim, metrafenona, boscalid, triticonazol, metconazol, dimetomorf, fenpropimorf, procloraz, vinclozolin, iprodiona, ditianon, metiram, tebuconazol, azoxistrobin, mancozeb, trifloxistrobin, clorotalonila, metalaxila, fosetila, difemoconazol, ciprodinila, espiroxamina, protioconazol, picoxistrobin.
Todas as formas de realização das formulações como definido acima são referida as seguir como “formulação de acordo com a presente invenção”.
A presente invenção além disso, diz respeito a um método de combater insetos nocivos e/ou fungos fitopatogênicos, que compreendem contatar os ditos insetos nocivos e/ou os fungos fitopatogênicos, seu hábito, solo de criação, fornecimento de alimentos, planta, semente, solo, área, material ou ambiente em que os insetos nocivos e/ou fungos fitopatogênicos estão se desenvolvendo ou podem se desenvovler ou os materiais, plantas, sementes, solos, superfícies ou espaços a serem protegidos do ataque ou infestação pelos ditos insetos nocivos e/ou fungos fitopatogênicos com uma 5 quantidade eficaz de uma formulação agroquímica de acordo com a presente invenção.
Desta maneira, as formulações de acordo com a presente invenção podem ser, portanto, usadas para controlar uma multitude de fungos fitopatogênicos ou insetos em várias plantas ou ervas cultivadas, tais como 10 trigo, centeio, cevada, aveias, arroz,, milho, grama, bananas, algodão, soja, café, cana de açúcar, parreiras, frutas e plantas ornamentais e vegetais, tais como pepinos, feijões, tomates, batatas e cucúrbitas e nas sementes destas plantas.
A presente invenção, além disso, diz respeito a um método de 15 controlar vegetação indesejada e/ou um método de regulação do desenvolvimento de plantas, que compreende deixar uma quantidade herbicidamente ou reguladora de desenvolvimento eficaz de uma formulação agroquímica de acordo com a presente invenção atuar nas plantas, seu habitat ou na semente das ditas plantas.
O termo fungos fitopatogênicos inclui, mas não é limitado às
seguintes espécies:
Alternaria spp. Em arroz, vegetais, sojas, canola/óleo de semente de colza e beterraba de açúcar e frutas, Afanomyces spp. em beterraba de açúcar e vegetais, Bipolaris e Drechslera spp. em milho, cereais, 25 arroz e turfa, Blumeria graminis (míldio em pó) em cereais, Botritis cinerea (mofo cinza) em morango, vegetais, ornamentais e parreiras, Bremia lactucae em alface Cercospora spp. em milho, sojas e beterraba de açúcar Cochliobolus spp. em milho, cereais em arroz (por exemplo Cochliobolus sativus em cereais, Cochliobolus miyabeanus em cerais) Colletotrichum spp. em sojas e algodão Drechslera spp. em cereais e milho Exserohilum spp. em milho Erysiphe cichoracearum e Sfaerotheca fiiliginea em cucúrbitas, Erysiphe necator em parreiras Fusarium e Verticillium spp. em várias plantas, Gaeumannomyces graminis em cereais Gibberella spp. em cereais e arroz 5 (por exemplo Gibberella fujikuroi em cerais, Gibberella zeae em cereais) complexo de tingimento de grãos em cerais Microdochium nivale em cereais Mycosfaerella spp. em cereais, bananas e amendoins, Fakopsora pachyrhizi e Fakopsora meibomiae on sojas Fomopsis spp. em sojas e girassol Phytophtora infestans em batatas e tomates, Plasmopara viticola em parreiras, Podosfaera 10 leucotricha em maçãs, Pseudocercosporella herpotrichoides em trigo e cevada, Pseudoperonospora spp. em lúpulos e pepinos, Puccinia spp. em cereais e milho, Pirenofora spp. em cereais Piricularia oryzae em cerais, Cochliobolus miyabeanus e Corticium sasakii (Rhizoctonia solani), Fusarium semitectum (e/ou moniliforme), Cercospora oryzae, Sarocladium oryzae, S 15 attenuatum, Entiloma oryzae, Gibberella fujikuroi (bakanae), Grainstaining complex (vários patogênios), Bipolaris spp., Drechslera spp. e Pytium e Rhizoctonia spp. em cerais, milho, algodão, canola, óleo de semente de colza, girassol, beterraba de açicar, vegetais, turfa, nozess e outras várias plantas Rhizoctonia solani em batata Sclerotinia spp. em canola/óleo de semente de 20 colza e girassol Septoria tritici e Stagonospora nodorum no trigo, Uncinula necator em parreiras, Sfacelotheca reiliana em milho Tievaliopsis spp. em sojas e algodão Tilletia spp. em cereais Ustilago spp. em cereais milho e cana de açúcar e Venturia spp. (crosta) em maçãs e pêras;
O termo pragas de insetos nocivos incluem mas não limitam-se aos seguintes artrópodes e nematódeos:
milípedes (Diplopoda) tais como a espécie Blaniulus Formigas (Hymenoptera), tais como, Atta capiguara, Atta cefalotes, Atta laevigata, Atta robusta, Atta sexdens, Atta texana, Monomorium faraonis, Solenopsis geminata, Solenopsis invicta, espécies Pogonomyrmex e Pheidole megacefala,
Besouros (Coleoptera), tais como Agrilus sinuatus, Agriotes lineatus, Agriotes obscurus e outras espécies, Amphimallus solstitialis, Anisandrus dispar, Antonomus grandis, Antonomus pomorum, Aracanthus morei, Atomaria linearis, espécie Blapstinus, Blastofagus piniperda, Blitofaga undata, Bothynoderes punciventris, Bruchus rufimanus, Bruchus pisorum, Bruchus lentis, Byctiscus betulae, Cassida nebulosa, Cerotoma trifurcata, Ceutorrhynchus assimilis, Ceutorrhynchus napi, Chaetoenema tibialis, Conoderus vespertinus e outras espécies Conoderus, Conorhynchus mendicus, Crioeeris asparagi, Cilindrocopturus adspersus, Diabrotiea (Iongicomis) barberi, Diabrotiea semi-punctata, Diabrotiea speciosa, Diabrotiea undecimpunctata, Diabrotiea virgifera e outras espécies Diabrotica, espécies Eleodes, Epilachna varivestis, Epitrix hirtipennis, Eutinobothrus brasiliensis, Hilobius abietis, Hypera brunneipennis, Hypera postiça, Ips typographus, Lema bilineata, Lema melanopus, Leptinotarsa decemlineata, Limonius califomicus e outras espécies Limonius, Lissorhoptrus oryzophilus, Listronotus bonariensis, Melanotus communis e outras espécies Melanotus, Meligethes aeneus, Melolonta hippocastani, Melolonta melolonta, Oulema oryzae, Ortiorrhynchus sulcatus, Oryzofagus oryzae, Otiorrhynchus ovatus, Oulema oryzae, Faedon cochleariae, Phillotreta chrysocefala, Phillofaga cuyabana e outras espécies Phillofaga, Philloperta horticola, Phillotreta nemorum, Phillotreta striolata e outras espécies Phillotreta, Popillia japonica, Promecops carinicollis, Premnotripes voraz, espécies Psilliodes, Sitona lineatus, Sitophilus granaria, Stemechus pinguis, Stemechus subsignatus e Tanymechus palliatus e outras espécies Tanymechus,
Moscas (Diptera), tais como Agromyza oryzea, Chrysomya bezziana, Chrysomya hominivorax, Chrysomya macellaria, Contarinia sorghicola, Cordilobia anthropofaga, Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Delia antique, Delia coarctata, Delia platura, Delia radicum, Fannia canicularis, Gasterophilus intestinalis, Geomyza Tripunctata, Glossina morsitans, Haematobia irritans, Haplodiplosis equestris, Hypoderma lineata, Liriomyza sativae, Liriomyza trifolii, Lucilia caprina, Lucilia cuprina, Lucilia sericata, Lycoria pectoralis, Mayetiola destructor, Museina stabulans, 5 Oestrus ovis, Opomyza florum, Oseinella frit, Pegomya hysociami, Forbia antiqua, Forbia brassicae, Forbia coarctata, Progonya leyoscianii, Psila rosae, Rhagoletis cerasi, Rhagoletis pomonella, Tabanus bovinus, Tetanops myopaeformis, Tipula oleracea e Tipula paludosa,
Heteropteranos (Heteroptera), tais como Acrostemum hilare, 10 Blissus leucopterus, Cicadellidae tais como Empoasca fabae, Chrysomelidae, Cirtopeltis notatus, Delpahcidae, Dysdercus cingulatus, Dysdercus intermedius, Eurygaster integriceps, Euschistus impictiventris, Leptoglossus phillopus, Lygus lineolaris, Lygus pratensis, Nefotettix species, Nezara viridula, Pentatomidae, Piesma quadrata, Solubea insularis e Thyanta perditor, 15 Afídeos e outros homopteranos (Homoptera), por exemplo
Acirtosifon onobrychis, Adelges laricis, Aphidula nasturtii, Aphis fabae, Aphis forbesi, Aphis glicines, Aphis gossypii, Aphis grossulariae, Aphis pomi, Aphis schneideri, Aphis spiraecola, Aphis sambuci, Acirtosifon pisum, Aulacorthum solani, Brachycaudus cardui, Brachyeaudus helichrysi, 20 Brachyeaudus persicae, Brachyeaudus prunicola, Brevieoryne brassicae, Capitoforus homi, Cerosifa gossypii, Chaetosifon fragaefolii, Cryptomyzus ribis, Dreyfusia nordmannianae, Dreyfusia piceae, Dysaphis radicola, Dysaulacorthum pseudosolani, Dysaphis plantaginea, Dysaphis piri, Empoasca fabae, Hyalopterus pruni, Hyperomyzus lactucae, Macrosiphum 25 avenae, Maerosiphum euforbiae, Maerosifon rosae, Megoura viciae, Melanaphis pirarius, Metopolophium dirhodum, Myzodes (Myzus) persicae, Myzus ascalonicus, Myzus cerasi, Myzus varians, Nasonovia ribis-nigri, Nilaparvata lugens, Pemphigus bursarius, Pemphigus populivenae, e outras espécies Pemphigus, Perkinsiella saccharicida, Forodon humuli, Psillidae tais como Psilla mali, Psilla piri e outras espécies de Psilla, Rhopalomyzus ascalonicus, Rhopalosiphum maidis, Rhopalosiphum padi, Rhopalosiphum insertum, Sappaphis mala, Sappaphis mali, Schizaphis graminum, Schizoneura lanuginosa, Sitobion avenae, Trialeurodes vaporariorum, 5 Toxoptera aurantiiand e Viteus vitifolii;
Lepidopteranos (Lepidoptera), por exemplo, Agrotis ypsilon, Agrotis segetum e outras espécies Agrotis, Alabama argillacea, Anticarsia gemmatalis, Argyrestia conjugella, Autografa gamma, Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheimatobia brumata, Chilo 10 suppresalis e outras espécies Chilo, Choristoneura fumiferana, Choristoneura occidentalis, Cirphis unipuncta, Cnaphlocrocis medinalis, Cidia pomonella, Dendrolimus pini, Diafania nitidalis, Diatraea grandiosella, Earias insulana, Elasmopalpus lignosellus, Eupoecilia ambiguella, espécies Euxoa, Evetria bouliana, Feltia subterranea, Galleria mellonella, Grafolita funebrana, 15 Grafolita molesta, Heliotis armigera, Heliotis virescens, Heliotis zea, Hellula undalis, Hibemia defoliaria, Hyfantria cunea, Hyponomeuta malinellus, Keiferia lycopersicella, Lambdina fiscellaria, Laphygma exigua, Lerodea eufala, Leucoptera coffeella, Leucoptera scitella, Litocolletis blancardella, Lobesia botrana, Loxostege sticticalis, Lymantria dispar, Lymantria monacha, 20 Lyonetia clerkella, Malacosoma neustria, Mamestra brassicae, Momphidae, Orgyia pseudotsugata, Ostrinia nubilalis, Panolis flammea, Pectinofora gossypiella, Peridroma saucia, Falera bucefala, Phtorimaea operculella, Phillocnistis citrella, Pieris brassicae, Plathypena scabra, Plutella xilostella, Pseudoplusia includens, Rhyacionia frustrana, Scrobipalpula absoluta, 25 Sesamia nonagrioides e outras espécies Sesamia, Sitotroga cerealella, Sparganotis pilleriana, Spodoptera frugiperda, Spodoptera littoralis, Spodoptera litura, Taumatopoea pityocampa, Tortrix viridana, Trichoplusia ni e Zeiraphera canadensis,
ortopteranos (Ortoptera), tais como Acrididae, Acheta domestica, Blatta orientalis, Blattella germanica, Forficula auricularia, Grillotalpa grillotalpa, Locusta migratória, Melanoplus bivittatus, Melanoplus femur-rubrum, Melanoplus mexicanus, Melanoplus sanguinipes, Melanoplus spretus, Nomadacris septemfasciata, Periplaneta americana, Schistocerca 5 americana, Schistocerca peregrina, Stauronotus maroccanus and Tachycines asynamorus;
térmites (Isoptera), tais como Calotermes flavicollis, Coptotermes species, Dalbulus maidis, Leucotermes flavipes, Macrotermes gilvus, Reticulitermes lucifugus e Termes natalensis;
tripse (Thysanoptera), tais como Frankliniella fusca,
Frankliniella occidentalis, Frankliniella tritici e outras espécies Frankliniella, Scirtothrips citri, Thrips oryzae, Thrips palmi, Thrips simplex e Thrips tabaci,
Arachnoidea, tais como aracnídeos (Acarina), por exemplo, das famílias Argasidae, Ixodidae e Sarcoptidae, tais como Amblyomma americanum, Amblyomma variegatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Dermacentor silvarum, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Omitodorus moubata, Otobius megnini, Dermanyssus gallinae, Psoroptes ovis, Rhipicefalus appendiculatus, Rhipicefalus evertsi, Sarcoptes scabiei e Eriophyidae species, tais como Aculus schlechtendali, Phillocoptrata oleivora e Eriophyes sheldoni; Tarsonemidae species, tais como Phytonemus pallidus e Polyfagotarsonemus latus; espécies Tenuipalpidae, tais como Brevipalpus foenicis; espécies Tetranychidae, tais como Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius e Tetranychus urticae, Panonychus ulmi, Panonychus citri e Oligonychus pratensis;
Nematódeos, especialmente nematódeos parasíticos de plantas, tais como nematódeos de nó de raiz, Meloidogyne hapla, Meloidogyne incógnita, Meloidogyne javanica e outras espécies Meloidogyne; nematódeos formadores de cisto, Globodera rostochiensis e outras espécies Globodera; Heterodera avenae, Heterodera glicines, Heterodera schachtii, Heterodera trifolii e outras espécies Heterodera; nematódeos de escoriação de semente, espécies Anguina; nematódeos de tronco e foliares, espécies Aphelenchoides;
5 nematódeos de espinho, Belonolaimus longicaudatus e outras espécies Beíonolaimus; nmatódeos de pinheiro, Bursaphelenchus xilophilus e outras espécies Bursaphelenchus; nematódeos de anel, espécies Criconema, espécies Criconemella, espécies Criconemoides, espécies Mesocriconema; nematódeos de tronco e bulbo, Ditilenchus destructor, Ditilenchus dipsaci e outras 10 espécies Ditilenchus species; nematódeos furadores, espécies Dolichodorus; nematódeos em espiral, Heliocotilenchus multicinctus e outras espécies Helicotilenchus; nematódeos de bainha e sheatoid, espécies Hemicicliofora e espécies Hemicriconemoides; espécies Hirshmanniella; nematódeos de lança, espécies Hoploaimus; nematódeos de nó de raiz falsos, espécies Nacobbus; 15 nematódeos agulha, Longidorus elongatus e outras espécies Longidorus; nematódeos de lesão, Pratilenchus neglectus, Pratilenchus penetrans, Pratilenchus curvitatus, Pratilenchus goodeyi e outras espécies Pratilenchus; nematódeos cavadores, Radofolus similis e outras espécies Radofolus; nematódeos reniformes, Rotilenchus robustus e outras espécies Rotilenchus; 20 espécies Scutellonema; nematódeos de raiz dura, Trichodorus primitivus e outras espécies Trichodorus, espécies Paratrichodorus; nematódeos que atrasam o desenvolvimento, Tilenchorhynchus claytoni, Tilenchorhynchus dubius e outras espécies Tilenchorhynchus; nematódeos cítricos, espécies Tilenchulus; nematódeos punhal, espécies Xiphinema e outros nematódeos 25 parasíticos vegetais.
O controle de vegetação indesejada é entendido como a destruição de ervas. As ervas, no sentido mais amplo, são entendidas significando todas aquelas plantas que se desenvolvem em locais onde estas são indesejadas. Como mencionado acima, em uma forma de realização dos métodos de combater fungos nocivos e/ou insetos, a formulação de acordo com a invenção também podem ser usados para o tratamento de sementes de plantas.
5 A presente invenção também compreende sementes revestidas
com formulação de acordo com a presente invenção.
O termo semente abrange sementes e propagules de plantas de todos os tipos incluindo, mas não limitado a sementes verdadeiras, pedaços de semente, brotos, cormos, bulbos, frutos, tubérculos, grãos, cortes, brotos de corte e outros e significa, em uam forma de realização preferida, sementes verdadeiras.
A semente adequada é semente de cereais, lavouras de raiz, lavouras oleosas, vegetais, temperos, ornamentais, por exemplo, semente de durum e outro trico, cevada, aveias, centeio, milho (milho de forragem e 15 milho de açúcar / milho doce e de campo), sojas, lavouras de óleo, crucífera, algodão, girassóis, bananas, arroz, óleo de semente de colza, nabo, beterraba de açúcar, beterraba de forragem, beringela, batatas, grama, gramado, turfa, grama de forragem, tomates, alho poró, abóbora/aboboreira, repolho, alface, pimenta, pepinos, melões, espécies Brassica, melões, feijões, ervilhas, alho, 20 cebolas, cenouras, plantas tuberosas, tais como batatas, cana de açúcar, tabaco, uvas, petúnias, gerânio / pelargônios, pansies e impatiens.
Além disso, a formulação de acordo com a invenção também pode ser usada para o tratamento de sementes de plantas, que toleram a ação de herbicidas ou fungicidas ou inseticidas devido à procriação, incluindo 25 métodos de engenharia genética, por exemplo, sementes de lavouras transgênicas que são resistentes a herbicidas do grupo que consiste das sulfoniluréias (EP-A-0257993, Patente U. S. N0 5,013,659), imidazolinonas (ver, por exemplo, US 6222100, WOO182685, W00026390, W09741218, W09802526, W09802527, WO 04/106529, WO 05/20673, WO 03/14357, WO 03/13225, WO 03/14356, WO 04/16073), tipo glufosinato (ver, por exemplo, EP-A-0242236, EP-A-242246) ou tipo glifosato (ver, por exemplo, WO 92/00377) ou em sementes de plantas resistentes a herbicidas selecionados do grupo de herbicidas de cicloexadienona/ácido ariloxifenoxipropiônico (US 5.162.602, US 5.290.696, US 5.498.544, US 5.428.001, US 6.069.298, US 6.268.550, US 6.146.867, US 6.222.099, US 6.414.222) ou em sementes de plantas de lavoura transgênica, por exemplo, algodão, com a capacidade de produzir toxinas de Bacillus thuringiensis (toxinas de Bt) que tomam as plantas resistentes a certas pragas (EP-A- 0142924, EP-A-0193259)
A aplicação de tratamento de semente da formulação de acordo com a invenção é realizada pela pulvarização ou polvilhamento das sementes antes de semenar as plantas e antes da emergência das plantas pelos métodos conhecidos pelo técnico habilitado.
No tratamento das sementes, as formulações correspondentes são aplicadas pelo tratamento das sementes com uma quantidade eficaz da formulação de acordo com a presente invenção. Aqui, as taxas de aplicação de pesticida são, no geral, de 0,1 g a 10 kg por 100 kg de semente, preferivelmente de 1 g a 5 kg por 100 kg de semente, em particular de 1 g a 2,5 kg por 100 kgde semente. Para lavouras específicas, tal como alface ou cebola, a taxa pode ser mais alta. A presente invenção fornece diversas vantagens sobre as formulações agroquímicas conhecidas: um ou ainda mais do que um pesticida podem ser mantidos em suspensão estável. Adicionalmente, um óleo pode ser adicionado à formulação. Além disso, a toxicidade da formulação é diminuída reduzindo-se a concentração de solventes orgânicos em comparação com os concentrados emulsificáveis ou pela redução da quantidade de pesticida, que é dissolvido no solvente orgânico. Uma vantagem adicional é que não existe risco de cristalização de pesticidas na fase de emulsão em temperatura mais baixa ou durante a armazenagem, porque o óleo é essencialmente isento de pesticida.
A invenção ainda é ilustrada mas não limitada pelos seguintes
exemplos.
Exemplo 1 - Preparação de uma formulação que compreende alfa-cipermetrina e fipronila
A) Preparação da pré-mistura
Uma solução de 280 g de água, 0,75 g de ácido cítrico, 2 g de Acticide MBS (l,2-Benzisotiazol-3(2H)-ona + 2-Metil-2H-isotiazol-3-ona), 83,3 g de Pluronic PE 10500 (tensoativo não iônico, copolímero de bloco de 10 óxido de etileno propileno da BASF, 18 % em peso em água) e 100 g de Soprofor FLK (trisitrilfeniletoxilato iônico da Rhodia), foram preparados pela agitação em um recipiente (até dissolver). Posteriormente, 180 g de fipronil e depois 120 g de alfa-cipermetrina foram adicionados sob condições de agitação. Depois 2,5 g de Rodorsil 416 (agente anti-espumante de 15 dialquilpolissiloxano, da Rhodia) e 0,5 g Rhodorsil 432 (agente anti- espumante de dialquilpolissiloxano, da Rhodia) foram adicionados até a mistura resultante ser homogênea.
A suspensão resultante foi então passada através de um moinho pérolas horizontal (pérolas de vidro ou de zircônio) até uma especificação de tamanho de partícula (80 % < 2 mícrons) ser atingida. Após a trituração, 0,75 g de goma xantana (espessador) foi adicionado sob condições de agitação e agitado até dissolver.
B) Preparação da fase oleosa
Em um recipiente separado, 300 g de óleo de milho e 20 g de um alcoxilado de álcool da fórmula (Ib) (GT2624 da AKZO) foram msiturados com um agitador até um mlíquido claro ser atingido.
C) Preparação do produto final
320 g da fase oleosa foram adicionados a 770,75 g de pré- mistura triturada (a quantidade depende da pureza dos ingredientes particulares) e combinados por uma trituração colóide até este ser homogêneo.
Exemplo Comparativo
O procedimento do Exemplo 1 foi repetido, em que o 5 alcoxilato de álcool da fórmula (Ib) na etapa B) foi substituído por uma mistura comercial de ésteres de polietileno de ácido graxo (Geronol ® VO 2001, um emulsificante da Rodhia) ou por éster de polietilenoglicol 300 de ácido 9-octadecenóico (Alkamuls ® A, um emulsificador não iônico da Rodhia). Em ambos os casos a formulação não foi estável e separada.
Claims (10)
1. Formulação, caracterizada pelo fato de que compreende (a) pelo menos um pesticida e (b) pelo menos um tensoativo não iônico da fórmula I R1-O-(AO)x-(H) (I) em que R1 representa alquila de cadeia reta ou ramificada tendo de 4 a 20 átomos de carbono; AO é etilenoóxi, propilenoóxi ou uma mistura de etilenoóxi e propilenoóxi; e x corresponde aos valores de 2 a 30 e (c) pelo menos um alcoxilato de tristirilfenila iônico e (d) pelo menos um óleo e (e) água, em que o pesticida está presente na fase aquosa na forma de uma suspensão e a concentração do pesticida no óleo não está excedendo 5 % em peso em relação ao peso total do óleo.
2. Formulação de acordo com a reivindicação 1, caracterizada pelo fato de que, adicionalmente, compreende pelo menos um solvente (f).
3. Formulação de acordo com qualquer uma das reivindicações de 1 a 2, caracterizada pelo fato de que o tensoativo não iônico (b) compreende a fórmula (Ib) R1-O-(A)n-(B)m-(H) (Ib) em que R1 representa alquila de cadeia reta ou ramificada tendo de 4 a átomos de carbono; A é etilenoóxi; B é propilenoóxi; e n, m corresponde aos valores de I a 10 contanto que a soma de m, n é pelo menos 2.
4. Formulação, de acordo com a reivindicação 3, caracterizada pelo fato de que na fórmula Ib do tensoativo não iônico (b) R1 representa 2- etilexila.
5. Formulação de acordo com qualquer uma das reivindicações de 1 a 4, caracterizada pelo fato de que o componente (c) representa um etoxilado de tristirilfenol iônico fosfatado ou sulfatado iônico.
6. Formulação de acordo com qualquer uma das reivindicações de 1 a 6, caracterizada pelo fato de que adicionalmente compreende um tensoativo não iônico adicional (f) selecionado do grupo consistindo de copolímeros em bloco de etilenoóxido / propilenoóxido.
7. Formulação de acordo com qualquer uma das reivindicações de 1 a 6, caracterizada pelo fato de que o óleo é isento de pesticida.
8. Método de combater insetos nocivos e/ou fungos fitopatogênicos, caracterizado pelo fato de que compreende contatar os ditos insetos nocivos e/ou fungos fitopatogênicos, seu habitat, local de criação, fornecimento de alimento, planta, semente, solo, área, material ou ambiente em que os insetos nocivos e/ou fungos fitopatogênicos estão se 20 desenvolvendo ou podem ser desenvolver ou os materiais, plantas, sementes, solos, superfícies ou espaços a serem protegidos de ataque ou infestação pelos ditos insetos nocivos e/ou fungos fitopatogênicos com uma quantidade eficaz de uma formulação agroquímica como definida em qualquer uma das reivindicações de 1 a 7.
9. Método de controlar vegetação indesejada, caracterizado pelo fato de que compreende deixar uma quantidade herbicidamente eficaz de uma formulação agroquímica como definida em qualquer uma das reivindicações de 1 a 7 atuar em plantas, seu habitat ou semente das ditas plantas.
10. Sementes, caracterizadas pelo fato de que são tratadas com uma formulação como definida em qualquer uma das reivindicações de 1 a 7.
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| RU2238649C1 (ru) | 2003-06-19 | 2004-10-27 | Закрытое акционерное общество "Щелково Агрохим" | Фунгицидная композиция на основе тебуконазола |
| WO2005065630A1 (ja) | 2004-01-06 | 2005-07-21 | Shiseido Co., Ltd. | 一相マイクロエマルション組成物、o/w超微細エマルション外用剤、及びその製造方法 |
| DE102004021434A1 (de) | 2004-04-30 | 2005-11-24 | Basf Ag | Schnelle schaumarme Netzer für hydrophobe Oberflächen |
| RU2370955C2 (ru) | 2004-09-13 | 2009-10-27 | Сертис Юроп Бв | Препарат для протравливания семян |
| US20080153706A1 (en) * | 2005-04-26 | 2008-06-26 | Bayer Cropscience Ag | Water-In-Oil Suspoemulsions |
| ES2331628T3 (es) | 2005-08-11 | 2010-01-11 | Basf Se | Mezclas plaguicidas que comprenden una fenilsemicarbazona. |
| AR056808A1 (es) | 2005-11-18 | 2007-10-24 | Cheminova As | Formulacion de aceite en agua de avermectinas |
| WO2007110355A2 (en) | 2006-03-24 | 2007-10-04 | Basf Se | Liquid non aqueous agrochemical formulations comprising distyrylphenol ethoxylate |
| EA016612B1 (ru) * | 2006-08-04 | 2012-06-29 | Басф Се | Неводные или водные концентраты действующего вещества с гербицидным действием, их применение и способ борьбы с нежелательным ростом растений |
| ES2340549T3 (es) | 2006-10-13 | 2010-06-04 | Rhodia Operations | Composicion disolvente que comprende al menos dos disolventes, y formulacion fitosanitaria que comprende dicha composicion disolvente asi como un compuesto activo. |
| CN101848639A (zh) * | 2007-07-20 | 2010-09-29 | 巴斯夫欧洲公司 | 含有醇烷氧基化物的组合物以及醇烷氧基化物在农业化学领域作为辅助剂的用途 |
| PL2184993T3 (pl) * | 2007-08-08 | 2012-03-30 | Basf Se | Wodne mikroemulsje zawierające owadobójcze związki organiczne |
| US20110105333A1 (en) * | 2007-08-16 | 2011-05-05 | Rafel Israels | Seed Treatment Compositions and Methods |
| AR071533A1 (es) * | 2008-05-02 | 2010-06-23 | Basf Se | Microemulsion mejorada con un amplio rango de aplicacion |
| WO2010010005A2 (de) | 2008-07-24 | 2010-01-28 | Basf Se | Öl-in-wasser emulsion umfassend lösungsmittel, wasser, tensid und pestizid |
-
2007
- 2007-11-09 US US12/515,749 patent/US8178117B2/en active Active
- 2007-11-09 CN CNA2007800434846A patent/CN101541167A/zh active Pending
- 2007-11-09 JP JP2009537598A patent/JP5260540B2/ja not_active Expired - Fee Related
- 2007-11-09 UA UAA200906189A patent/UA98128C2/ru unknown
- 2007-11-09 MX MX2009004923A patent/MX297198B/es active IP Right Grant
- 2007-11-09 CA CA2668968A patent/CA2668968C/en not_active Expired - Fee Related
- 2007-11-09 KR KR1020097012781A patent/KR101526016B1/ko active Active
- 2007-11-09 BR BRPI0719027-1A patent/BRPI0719027A2/pt not_active Application Discontinuation
- 2007-11-09 PH PH12009500961A patent/PH12009500961A1/en unknown
- 2007-11-09 AU AU2007324614A patent/AU2007324614B2/en active Active
- 2007-11-09 EA EA200900653A patent/EA019134B1/ru not_active IP Right Cessation
- 2007-11-09 WO PCT/EP2007/062110 patent/WO2008061899A2/en not_active Ceased
- 2007-11-09 EP EP07822411A patent/EP2107869A2/en not_active Ceased
- 2007-11-21 PE PE2007001622A patent/PE20081218A1/es not_active Application Discontinuation
- 2007-11-22 TW TW096144347A patent/TW200829161A/zh unknown
- 2007-11-22 AR ARP070105193A patent/AR063905A1/es active IP Right Grant
- 2007-11-22 CL CL200703342A patent/CL2007003342A1/es unknown
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2009
- 2009-05-08 CR CR10783A patent/CR10783A/es not_active Application Discontinuation
- 2009-06-15 EC EC2009009429A patent/ECSP099429A/es unknown
- 2009-06-18 ZA ZA200904264A patent/ZA200904264B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AR063905A1 (es) | 2009-02-25 |
| KR20090105917A (ko) | 2009-10-07 |
| EA200900653A1 (ru) | 2009-12-30 |
| CA2668968A1 (en) | 2008-05-29 |
| PH12009500961A1 (en) | 2008-05-29 |
| EA019134B1 (ru) | 2014-01-30 |
| WO2008061899A3 (en) | 2009-03-05 |
| AU2007324614A1 (en) | 2008-05-29 |
| ECSP099429A (es) | 2009-07-31 |
| CN101541167A (zh) | 2009-09-23 |
| UA98128C2 (ru) | 2012-04-25 |
| ZA200904264B (en) | 2010-08-25 |
| EP2107869A2 (en) | 2009-10-14 |
| AU2007324614B2 (en) | 2012-12-20 |
| MX2009004923A (es) | 2009-05-19 |
| JP2010510279A (ja) | 2010-04-02 |
| WO2008061899A2 (en) | 2008-05-29 |
| JP5260540B2 (ja) | 2013-08-14 |
| CA2668968C (en) | 2014-01-21 |
| CR10783A (es) | 2009-07-23 |
| US8178117B2 (en) | 2012-05-15 |
| US20100016155A1 (en) | 2010-01-21 |
| TW200829161A (en) | 2008-07-16 |
| KR101526016B1 (ko) | 2015-06-04 |
| PE20081218A1 (es) | 2008-11-06 |
| CL2007003342A1 (es) | 2008-07-04 |
| MX297198B (es) | 2012-03-16 |
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