CN103269591A - Herbicide combination with a dimethoxytriazinyl-ubstituted difluoromethanesulphonylanilide - Google Patents

Herbicide combination with a dimethoxytriazinyl-ubstituted difluoromethanesulphonylanilide Download PDF

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CN103269591A
CN103269591A CN2011800625318A CN201180062531A CN103269591A CN 103269591 A CN103269591 A CN 103269591A CN 2011800625318 A CN2011800625318 A CN 2011800625318A CN 201180062531 A CN201180062531 A CN 201180062531A CN 103269591 A CN103269591 A CN 103269591A
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plant
spp
acid
herbicidal combination
weed killer
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CN103269591B (en
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C·H·罗辛格
C·沃尔德拉夫
上野知惠子
E·哈克
白仓伸一
荒木恒一
中村新
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Bayer Intellectual Property GmbH
Bayer CropScience AG
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Bayer Pharma AG
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/661,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, 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
    • A01N43/80Biocides, 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

Abstract

The present invention relates to a herbicide combination, comprising components (A) and (B), where (A) denotes the compound described by the formula (A), and (B) denotes the compound described by the formula (B).

Description

Bag fluorinated ketones contained sulphur grass amine and Fen Nuo kill the grand Herbicidal combination of sulphur
The invention belongs to the technical field of crop production compositions, described crop combination thing can be by the preceding method (incorporate into or do not incorporate into) of for example sowing; before the bud behind method or the bud method be used for the undesired plant of crop plants opposing following sowing and plantation: wheat (durum wheat and common wheat) for example; corn; soybean; sugar beet; sugarcane; cotton; rice (under dry land or paddy field condition with the rice plantation of indica type or round-grained rice type kind and crossbreed/mutant/GMO or sowing); beans (for example bush bean and broad bean); flax; barley; oat; rye; triticale; rape; potato; broomcorn millet (Chinese sorghum); herbage; greenery patches/lawn; fruit plantation (plantation crops) or the non-crop zone (square of residential area or industrial area for example; railroad track).Except single administration, also can carry out sequential application.
The purposes that the present invention relates to comprise the Herbicidal combination of at least two kinds of weed killer herbicides and be used for the undesired plant of control; particularly comprise and be selected from N-{2-[4; 6-dimethoxy-(1; 3,5) triazine-2-(carbonyl-or-methylol)]-the 6-halogenophenyl } compound of difluoro methylsulfonyl amine or its N-methyl-derivatives and/or its salt (hereinafter being also referred to as " the difluoro mesyl aniline that is replaced by the dimethoxy-triazine base ") and the Herbicidal combination of other weeding active compounds.
Substituted sulfonamide has weeding (for example WO93/09099A2, WO96/41799A1) on the known ring.It also comprises phenyl difluoro Methanesulfomide (it is also referred to as difluoro mesyl aniline).Described phenyl difluoro Methanesulfomide compound is, for example, especially by dimethoxypyridin base (for example WO00/006553A1, JP2000-6336, JP11-060562) or dimethoxy-triazine base and the single replacement of other halogenic substituents (for example WO2005/096818A1, WO2007/031208A2) or polysubstituted phenyl derivatives.
Yet, from N-{2-[4,6-dimethoxy-(1,3,5) triazine-2 (carbonyl-or-methylol)]-the 6-halogenophenyl } particular compound (as being described in WO2005/096818A1) of difluoro methylsulfonyl amine and N-methyl-derivatives thereof be (as being described in WO2006/008159A1 about bactericide first, and be described in WO2007/031208A2 and WO2009/024251A2 as weed killer herbicide) with regard to its weeding, be not entirely satisfactory in all respects.
The difluoro mesyl aniline that is replaced by the dimethoxy-triazine base is to noxious plant (broad leaved weed, grassy weed, sedge (Cyperaceae); Hereinafter also be referred to as " weeds ") activity of weeding be in higher level, but depend on rate of application, used preparation, noxious plant or noxious plant spectrum, weather and soil condition etc. to be prevented and treated in each case usually.Other standards herein are the acting duration of weed killer herbicide or resolution ratio, general crop plants compatibility and the speed of action (the more quick acting of effect), activity profile and to the performance (multiple cropping problem) of succeeding crop or the overall flexibility of using (preventing and treating the weeds under its each vegetative stage).If suitable, can also need consider the variation of noxious plant susceptibility, it is in the long-term use of weed killer herbicide or may have (control of tolerance or resistant weed kind) in limited geographic area.Compensate for the loss of the activity of single plant only feasiblely to a certain extent by the rate of application that improves weed killer herbicide, this is because for example this operation can reduce the selectivity of weed killer herbicide, even or because improvement is not seen in effect yet when rate of application is higher.
Therefore, often need the specific weeds kind of opposing the target synergistic activity, have the control of weeds of better global selectivity, still less the reactive compound of consumption reaches equal and good prevent and treat result and minimizing and enter reactive compound in the environment usually, to avoid for example leaching and residual effect.Also need to develop disposable employed with repeatedly the using of the intensive that shuns labor, wherein, except the initial control fast of weeds, also there is slower aftereffect control (residual control) in and the system of exploitation control action speed.
The possible solution of the problems referred to above be can be provides Herbicidal combination; be the mixture of multiple weed killer herbicide and/or other components, described other components are selected from dissimilar agrochemically active compounds and are usually used in crop protection and formulation auxiliary agents and the additive of required additional features are provided.Yet, in being used in combination of various active compound, chemistry, physics or the inconsistent phenomenon of biology, for example antagonism of the biologic activity of the decomposition of coupling preparation deficient in stability, reactive compound or reactive compound often appear.For those reasons, must select potential suitable bond in the mode of target, and with its adaptability of experimental test, can not ignore passive result or the positive result of priori safely.
The mixture of the non-N-methyl-derivatives of above-claimed cpd is known (for example WO2007/079965A2) in principle; Yet, its with the mixture of other weed killer herbicides in effect only from the individual cases of the phenyl derivatives that replaced by the dimethoxypyridin base, confirm.In addition, the N-methyl-derivatives and some mixture in conjunction with component (for example WO2008/101595A2, WO2010/017930A2, WO2010/017931A2, WO2010/017929A1, WO2010/017922A2, WO2010/017921A2, WO2010/017924A2, WO2010/017923A2, WO2010/017928A1, DE102008037630, WO2010/017927A2, WO2010/017926A2, WO2010/017925A2) that also have the above-claimed cpd through selecting.
An object of the present invention is to provide crop production compositions as the substitute of prior art or as its improvement product.
Unexpectedly, have now found that purpose of the present invention can be by fluorine ketone sulphur grass amine (triafamone; The ISO common name of proposing)---a kind of weed killer herbicide that is selected from the N-methyl-derivatives of the difluoro mesyl phenyl amines that is replaced by the dimethoxy-triazine base---kills the grand (fenoxasulfone of sulphur with the fragrant promise of compound; The ISO common name of proposing) combination realizes, they are with a kind of particularly advantageous mode acting in conjunction, for example be used at crop plants sowing and/or plantation when it---wheat (durum wheat and common wheat) for example, corn, soybean, sugar beet, sugarcane, cotton, rice (under dry land or paddy field condition with the rice plantation of indica type and/or round-grained rice type kind and crossbreed/mutant/GMO or sowing), beans (for example, bush bean and broad bean), flax, barley, oat, rye, triticale, rape, potato, broomcorn millet (Chinese sorghum), herbage, greenery patches/lawn---in, (the square of residential area or industrial area for example in the fruit plantation on (plantation crops) or the non-crop zone, railroad track), particularly when preventing and treating undesired plant in the rice crops (under the condition in dry land or paddy field with the rice plantation of indica type and/or round-grained rice type kind and crossbreed/mutant/GMO or sowing).
Therefore, the invention provides a kind of Herbicidal combination, comprise component (A) and (B), wherein
(A) compound described by formula (A) of expression:
Figure BDA00003397318800031
And
(B) compound described by formula (B) of expression:
Compound (A) is weeding active compound and its reactive compound that is described to independent reactive compound and is combined with other weed killer herbicides in above at such document of quoting that is selected from the N-methyl-derivatives of the difluoro mesyl phenyl amines that is replaced by the dimethoxy-triazine base.Except characterizing with formula (A); described compound also is characterized by ISO common name fluorine ketone sulphur grass amine and the cycle chemistry title of proposal: 2 '-[(4,6-dimethoxy-1,3; 5-triazine-2-yl) carbonyl]-1; 1,6 '-three fluoro-N-methyl mesyl aniline (IUPAC) and N-[2-[(4,6-dimethoxy-1; 3; 5-triazine-2-yl) carbonyl]-the 6-fluorophenyl]-1,1-two fluoro-N-methyl Methanesulfomides (CA index name), and also be characterized by CAS registration number: 874195-61-6.
Component (B) is the compound that known conduct is used for the reactive compound of the undesired plant of control; Referring to, the document of quoting in JP2004-002324A and this specification for example.Except characterizing with formula (B); described compound also is characterized by the fragrant promise of ISO common name of proposal and kills the grand and cycle chemistry title of sulphur: 2; 5-two chloro-4-ethoxy benzyls 4; 5-dihydro-5; 5-dimethyl-1; 2-oxazole-3-base sulfone (IUPAC) or 3-[(2; 5-two chloro-4-ethoxy benzyls) sulfonyl]-4; 5-dihydro-5,5-dimethyl-1,2-oxazole (IUPAC) and 3-[[(2; 5-two chloro-4-ethoxyl phenenyls) methyl] sulfonyl]-4; 5-dihydro-5,5-dimethyl isoxazole (CA index name) also is characterized by CAS registration number: 639826-16-7 and is characterized by code name KUH-071 and KIH-1419.Under title KUH-071; this compound is mentioned (WO2010/017930A2 about the Herbicidal combination of the difluoro mesyl aniline that replaced by the dimethoxy-triazine base; WO2010/017931A2; WO2010/017929A1; WO2010/017922A2; WO2010/017921A2; WO2010/017924A2; WO2010/017923A2; WO2010/017928A1; DE102008037630; WO2010/017927A2; WO2010/017926A2; WO2010/017925A2); but it only summarily appears in the context of tabulation of other agrochemically active compounds, described other agrochemically active compounds may with each Herbicidal combination additional mixing of the present invention.Example about KUH-071 is not included in the above-mentioned document, and wherein also without any the hint that KUH-071 directly is used in combination with the compound that is selected from the difluoro mesyl phenyl amines that is replaced by the dimethoxy-triazine base.
Mentioned formula (A) and (B) contain all possible type of service, for example acid, salt, ester and isomer such as stereoisomer and optical isomer.Also specifically contain all stereoisomers and composition thereof, also have racemic mixture especially, and if---enantiomter is arranged---biologic activity enantiomter separately.It also is applicable to possible rotational isomer.The formation of possible salt can be undertaken by the compound that alkali is acted on have acid hydrogen atom.Suitable alkali is, organic amine for example is as trialkylamine, morpholine, piperidines or pyridine; And the hydroxide of ammonium, alkali metal or alkaline earth metal, carbonate and bicarbonate, particularly sodium hydroxide and potassium hydroxide, sodium carbonate and potash and sodium bicarbonate and saleratus; The alkoxide of alkali metal or alkaline earth metal, particularly sodium methoxide, caustic alcohol, normal propyl alcohol sodium, sodium isopropylate, n-butanol sodium or sodium tert-butoxide, or potassium methoxide, potassium ethoxide, normal propyl alcohol potassium, potassium isopropoxide, n-butanol potassium or potassium tert-butoxide.These salt are the compound that substituted by cation suitable on the agricultural of acidic hydrogen wherein, for example slaine, particularly alkali metal salt or alkali salt, especially sodium salt or sylvite, and perhaps ammonium salt, organic amine salt or quaternary ammonium salt for example have formula [NRR ' R " R " '] +Cationic compound, R to R wherein " ' be organic group, particularly alkyl, aryl, aralkyl or alkaryl separately independently of each other.Also that suitable is alkyl sulfonium salt and alkyl oxidation sulfonium salt, for example (C 1-C 4) triakylsulfonium salts and (C 1-C 4) trialkyl oxidation sulfonium salt.By suitable inorganic acid or organic acid---for example, inorganic acid such as HCl, HBr, H 2SO 4, H 3PO 4Or HNO 3Or organic acid such as carboxylic acid such as formic acid, acetic acid, propionic acid, ethanedioic acid, lactic acid or salicylic acid or sulfonic acid such as p-methyl benzenesulfonic acid---form adduct with basic group such as amino, alkyl amino, dialkyl amido, piperidyl, morpholinyl or pyridine radicals, the compound of formula (I) also can form salt.Then these salt comprise the conjugate base as the acid of anion.
Hereinafter, term " weed killer herbicide ", " independent weed killer herbicide ", " compound " or " reactive compound " also with context in term " component " use with the free burial ground for the destitute.
Component of the present invention (A) and Herbicidal combination (B) can comprise other other components: dissimilar agrochemically active compound and/or be usually used in formulation auxiliary agents and/or the additive of crop protection for example, or use with these components.Hereinafter, use term " Herbicidal combination " or " bond " also to comprise " herbicidal composition " that forms by this way.
In a preferred embodiment, Herbicidal combination of the present invention comprises the weed killer herbicide (A) of effective dose and (B) also/or have synergy.For example, when using weed killer herbicide (A) together and (B) can be observed synergy when (for example as common preparation or as the mixed thing of bucket); Yet, when using reactive compound (using respectively) in the different time, also can be observed synergy.Also can many parts use described weed killer herbicide or Herbicidal combination (sequential application), for example use then before the first bud and use behind the bud, perhaps use behind the earlier early stage bud, use behind mid-term or the later stage bud then.Preferred jointly or almost use the weed killer herbicide (A) of described bond and (B) simultaneously at this, and preferably use jointly especially.
Synergy can make rate of application reduction, the effectiveness under identical rate of application of single weed killer herbicide higher, the kind (clear band) that control is not is not also prevented and treated, control is to single weed killer herbicide or multiple herbicide tolerant or have the kind of resistance, the phase of using prolongs and/or required independent application times reduces, and---for the user---obtains control of weeds system more favourable on economy and ecology.
For example, the bond of weed killer herbicide of the present invention (A)+(B) makes and actively to strengthen so that unexpected mode is collaborative so far, exceeded to use single weed killer herbicide (A) and (B) accessible activity.
Weed killer herbicide (A) mainly suppresses acetolactate synthestase (ALS) thereby the biosynthesis of protein in the inhibition plant.The rate of application of weed killer herbicide (A) can change in wide region, for example at 0.1g to 1000g AS/ha (hereinafter, AS/ha represents " active substance/hectare "=based on the reactive compound meter of 100% purity).When using with the rate of application of 0.1 to 1000g AS/ha, when prior to seeding, before the plantation or before the bud and when using weed killer herbicide (A) in the method behind the bud, it can prevent and treat the noxious plant of wide relatively spectrum, for example annual and perennial unifacial leaf or dicotyledonous broad leaved weed, grassy weed and sedge, and undesired crop plants.For bond of the present invention, rate of application is lower usually, for example in the scope of 0.1 to 500g AS/ha, preferred 0.5g to 200g AS/ha, preferred especially 1g to 150g AS/ha.
The rate of application of weed killer herbicide (B) can change in wide region, 1g to 5000g AS/ha (hereinafter, AS/ha represents " active substance/hectare "=based on the reactive compound meter of 100% purity) for example, and it has wideer relatively noxious plant spectrum to be prevented and treated.For bond of the present invention, rate of application is lower usually, for example 1 to 1500g AS/ha, preferably 2 to 1000g AS/ha, particularly preferably in 3 to the 800g AS/ha scopes.
Compound (A) for example can be by deciding with reference to the rate of application of mentioned individualized compound with (B) suitable proportion.In bond of the present invention, can reduce rate of application usually.In bond of the present invention, in conjunction with weed killer herbicide (A) and (B) preferred mixing ratio (A): (B) standard is following weight ratio:
Component (A) and (B) weight ratio (A): (B) usually in 1: 1500 to 500: 1, preferred 1: 1000 to 100: 1, special 1: 200 to 20: 1 scope.
Preferred Herbicidal combination is following bond: it also comprises one or more and weed killer herbicide (A) and (B) different and also be used as other agrochemically active compounds of selective herbicide except bond of the present invention.
Herbicidal combination of the present invention also can comprise the various agrochemically active compounds as other extra components; for example be selected from safener, fungicide, insecticide, miticide, nematocide, bird repellent, soil structure conditioner, nutrient for plants (fertilizer) and structure and be different from weed killer herbicide (A) and weed killer herbicide (B) and plant growth regulator, or be selected from formulation auxiliary agents and the additive that is usually used in crop protection.
Therefore, other suitable weed killer herbicide is, for example structure is different from weed killer herbicide (A) and following weed killer herbicide (B), preferred its effect is based on the weeding active compound that suppresses following material, described material is acetolactate synthase for example, acetyl-CoA carboxylase, cellulose synthase, enol acetone shikimic acid-3-phosphate synthase, glutamine synthelase, to hydroxyphenyl pyruvic acid dioxygenase, phytoene dehydrogenase, light system I, light system II, proporphyrinogen oxidase, as be described in for example Weed Research26 (1986) 441-445 or " The Pesticide Manual ", 15th edition, The British Crop Protection Council and the Royal Soc.of Chemistry, 2006, and the document of wherein quoting.Can mention as being applicable to that known weed killer herbicide or the plant growth regulator of being combined with compound of the present invention are for example following reactive compound (described compound is according to the common name name of International Organization for Standardization or the compound of being named by chemical name or code name), and comprise all types of service separately, for example acid, salt, ester and isomer, for example stereoisomer and optical isomer.
Particularly advantageous is selectivity control noxious plant in the crop of useful plant and ornamental plants.Although described weed killer herbicide (A) and (B) in a large amount of crops, demonstrating good and even enough selectivity, in principle, in some crops, particularly also when mixing with the less weed killer herbicide of other selectivity, the phytotoxicity to crop plants may appear.Thus, comprising the weeding active compound of the combination according to the present invention and the weed killer herbicide of one or more safeners (A) is particularly advantageous with (B) bond.Described safener uses with the detoxifcation effective dose, important crop or in fruit plantation (plantation crops), reduce the plant toxicity side effect of used weed killer herbicide/agricultural chemicals economically for example, described important crop economically is cereal (wheat, barley, rye, oat, corn, rice, broomcorn millet), sugar beet, sugarcane, rape, cotton, soybean for example, preferred cereal is in particular rice.
Below for example be suitable for the compound group (comprising that possible stereoisomer and agricultural go up ester or salt commonly used) of making safener: benoxacor (benoxacor), cloquitocet_mexyl (cloquintocet (mexyl)) cyometrinil (cyometrinil), cyprosulfamide, dichlormide (dichlormid), dicyclonon, O-phenyl D2EHDTPA O, O-diethyl ester (dietholate), disulfoton (disulfoton) (=S-2-ethylmercapto group diethyldithioposphoric acid O, the O-diethyl ester), fenchlorazole (fenchlorazole (ethyl)), fenclorim (fenclorim), separate careless amine (flurazole), fluxofenim (fluxofenim) Xie Cao oxazole (furilazole) Shuan Ben oxazole acid (isoxadifen (ethyl)), mefenpyrdiethyl (mefenpyr (diethyl)), methyl carbamic acid 4-chlorphenyl ester (mephenate), naphthalic anhydride, oxabetrinil (oxabetrinil), " R-29148 " (=3-dichloro-acetyl-2,2,5-trimethyl-1, the 3-oxazolidine), " R-28725 " (=3-dichloro-acetyl-2,2-dimethyl-1, the 3-oxazolidine), " PPG-1292 " (=N-pi-allyl-N-[(1,3-dioxolanes-2-yl) methyl] dichloro acetamide), " DKA-24 " (=N-pi-allyl-N-[(allyl amino carbonyl) methyl] dichloro acetamide), " AD-67 " or " MON4660 " (=3-dichloro-acetyl-1-oxa--3-azaspiro [4,5] decane), " TI-35 " (=1-dichloro-acetyl azepan), " dimepiperate (dimepiperate) " or " MY-93 " (=piperidinyl-1-thiocarboxylic acid S-1-methyl isophthalic acid-phenyl chlorocarbonate), " daimuron (daimuron) " or " SK23 " (=1-(1-methyl isophthalic acid-phenylethyl)-3-p-methylphenyl urea), " cumyluron (cumyluron) " or " JC-940 " (=3-(2-Chlorophenylmethyl)-1-(1-methyl isophthalic acid-phenylethyl) urea, " methoxyphenone (methoxyphenone) " or " NK049 " (=3,3 '-dimethyl-4-methoxy benzophenone), " CSB " (=1-bromo-4-(chloromethyl sulfonyl) benzene), " CL-304415 " (=4-carboxyl-3,4-dihydro-2H-1-chromene-4-acetic acid; CAS registration number: 31541-57-8), " MG-191 " (=2-dichloromethyl-2-methyl isophthalic acid, 3-dioxolanes), " MG-838 " (=1-oxa--4-azaspiro [4.5] decane-4-carbodithioic acid 2-propylene ester; CAS registration number: 133993-74-5), (diphenyl methoxy base) methyl acetate (CAS registration number: 41858-19-9, from WO-A-1998/38856), [(3-oxo-1H-2-benzothiopyran derivative-4 (3H)-subunit) methoxyl group] methyl acetate (CAS registration number: 205121-04-6, from WO-A-1998/13361), 1,2-dihydro-4-hydroxyl-1-methyl-3-(5-tetrazole radical carbonyl)-2-quinolone (CAS registration number: 95855-00-8 is from WO-A-1999/000020).
More known safeners are used as weed killer herbicide, and correspondingly, except noxious plant is had the herbicide effect, also play the effect of cover crop plant.
The weight ratio of Herbicidal combination and safener depends on the effect of rate of application and the described safener of weed killer herbicide usually, and can in wide region, change, for example 90000: 1 to 1: 5000, preferably 7000: 1 to 1: 1600, especially in 3000: 1 to 1: 500 scopes.Can with weed killer herbicide (A) and (B) or the mixture of they and other weed killer herbicide/agricultural chemicals prepare described safener similarly, and with finished product preparation or to supply with and to use with the form of the mixed thing of bucket of described weed killer herbicide, perhaps use respectively with the form of seed, soil or foliage applying.
Herbicidal combination of the present invention (=Herbicidal combinations) is to the important unifacial leaf economically of wide range and dicotyledonous harmful plants for example broad leaved weed, grassy weed or sedge, comprise that the kind that weeding active compound is had a resistance has excellent herbicidal, described weeding active compound for glyphosate for example, Glufosinate, atrazine, imidazolinone herbicide, sulfonylurea, (mixing) aryloxy aromatic yloxy yl alkyl carboxylic acid or-Phenoxyalkylcarboxylacid acid (" fops "), cyclohexanedione oxime (" dims ") or auximone inhibitor.Described reactive compound also acts on the perennial weed that germinates and be difficult to prevent and treat from rhizome, root-like stock and other perennating organs effectively.At this, can for example jointly or respectively use described material by method behind method or the bud before the preceding method of for example sowing, the bud.Preference is as being applied to the noxious plant that has particularly germinateed by method behind the bud.
Can mention and to be not limited to some kind by monocotyledon weed and floral some representational instantiation of broadleaf weed of compound control of the present invention but enumerate.
The example of the weeds kind of described herbicidal composition useful effect is, for example the Avena of monocotyledon weed kind (Avena spp.), amur foxtail belongs to (Alopecurus spp.), false Agrostis (Apera spp.), Brachiaria (Brachiaria spp.), Brome (Bromus spp.), knotgrass (Digitaria spp.), Lolium (Lolium spp.), Echinochloa (Echinochloa spp.), Sprangletop (Leptochloa spp.), genus fimbristylis (Fimbristylis spp.), Panicum (Panicum spp.), phalaris arundinacea (Phalaris spp.), annual bluegrass belongs to (Poa spp.), setaria (Setaria spp.) and Cyperus annual weed such as (Cyperus); And the Agropyron in the perennial kind (Agropyron), Cynodon (Cynodon), cogon (Imperata) and sorghum and perennial Cyperus kind
For the broadleaf weed kind, action spectrum extends to the subordinate, abutilon (Abutilon spp.) for example, Amaranthus (Amaranthus spp.), Chenopodium (Chenopodium spp.), crowndaisy chrysanthemum belongs to (Chrysanthemum spp.), galium (Galium spp.), Ipomoea (Ipomoea spp.), Kochia (Kochia spp.), lamium (Lamium spp.), Matricaria (Matricaria spp.), ipomoea (Pharbitis spp.), Polygonum (Polygonum spp.), chrysanthemum harvest spp (Sida spp.), sinapsis alba belongs to (Sinapis spp.), Solanum (Solanum spp.), Stellaria (Stellaria spp.), Veronica (Veronica spp.), Eclipta prostrata belongs to (Eclipta spp.), Daubentonia (Sesbania spp.), Aeschynomene spp. and Viola (Viola spp.), Xanthium annual weed such as (Xanthium spp.) and japanese bearbind belong to (Convolvulus), Cirsium (Cirsium), Rumex (Rumex) and artemisia perennial weeds such as (Artemisia).
If the reactive compound with Herbicidal combination of the present invention before germinateing is applied to soil surface, prevent fully that then the weeds seedling from germinateing, perhaps weed growth is to cotyledon period, but it just stops growing then, and finally two thoughtful around after death fully.
If after germination, described reactive compound is applied to the green parts of plant, growth can just sharply stop in the suitable short time after processing equally, and the vegetative period when this ruderal plant remains on time of application point, perhaps it is fully dead after certain hour, thereby with the utmost point in this way early and eliminate the competition that is produced by the weeds that are harmful to crop plants constantly.For rice, also described reactive compound can be applied in the water, it is ingested by soil, bud and root then.
The characteristics of Herbicidal combinations of the present invention are rapid-action and long-acting herbicide effect.Usually, the resistance of rainwater washing against power of reactive compound is favourable in the bond of the present invention.A special advantage is that the dosage that uses in the described bond and compound (A) and effective dose (B) all are adjustable to lower level, so that its effect to soil is low to moderate optimum degree.This makes it at first not only can be applied to sensitive crop, has also almost avoided groundwater contamination.The bond of reactive compound of the present invention makes the required rate of application of reactive compound reduce significantly.
In a preferred embodiment, weed killer herbicide (A) and Herbicidal combination height of the present invention (B) are applicable to the noxious plant of optionally preventing and treating in the rice crops.Described rice crops is included in the institute of rice cultivation under the most diverse condition might form, and for example dry land is cultivated, cultivate in the nonirrigated farmland or cultivate in the paddy field, and wherein irrigating can be natural (rainfall) and/or artificial (pouring, flood irrigation).The seed (being obtained by sudden change or transgenosis) that the rice that is used for this purpose can be conventional seed, the hybrid seed of cultivating or has resistance---tolerance---at least, it can be derived by indica type or round-grained rice type kind or its crossbreed.
Can use Herbicidal combination of the present invention by the various application processes that are usually used in rice herbicides.Particularly preferably, it is used by spray application and/or by dipping.In dipping was used, when using, the water in paddy field had covered ground and had been up to 3-20cm.Then Herbicidal combination of the present invention is for example directly placed the water in paddy field with the form of granule.Worldwide, spray application is mainly used in the directly rice of sowing, and dipping is used the rice that is mainly used in transplanting.
Herbicidal combination of the present invention has covered wideer weeds spectrum, and described weeds spectrum especially has specificity to rice crops.For example following weeds are all had good control: in the monocotyledon weed with the subordinate, Echinochloa for example, Panicum, annual bluegrass belongs to, Sprangletop, Brachiaria, knotgrass, setaria, Cyperus, Monochoria (Monochoria spp.), genus fimbristylis, arrowhead belongs to (Sagittaria spp.), Eleocharis (Eleocharis spp.), Scirpus (Scirpus spp.), Waterplantain (Alisma spp.), leaf of bamboo Lepidium (Aneilema spp.), water screening spp (Blyxa spp.), eriocaulon buergerianum (Eriocaulon spp.), Potamogeton (Potamogeton spp.) etc. all prevents and treats finely, particularly following kind: water barnyard grass (Echinochloa oryzicola), Monochoria vaginalis (Monochoria vaginalis), yak grass (Eleocharis acicularis), scouring rush's shape water chestnut (Eleocharis kuroguwai), difformed galingale herb (Cyperus difformis), Herba Cyperi Glomerati (Cyperus serotinus), short arrowhead (Sagittaria pygmaea), alisma canaliculatum (Alisma canaliculatum), firefly Lin (Scirpus juncoides).Under the situation of broadleaf weed, activity profile extends to the subordinate, for example Polygonum; Han Lepidium (Rorippa spp.), joint joint Lepidium (Rotala spp.), Vandellia (Lindernia spp.), Bidens (Bidens spp.), cusp Pittosporum (Sphenoclea spp.), the horsefly eye belongs to (Dopatrium spp.), Eclipta prostrata belongs to (Eclipta spp.), Elatine ambigua (Elatine spp.), Gratiola (Gratiola spp.), Vandellia (Lindernia spp.), ludwigia (Ludwigia spp.), Oenanthe (Oenanthe spp.), Ranunculus (Ranunculus spp.), pool chilly genus (Deinostema spp.) etc.Particularly such as following kind: mexicana (Rotala indica), cusp flower (Sphenoclea zeylanica), Procumbent Falsepimpernel (Lindernia procumbens), false loosestrife (Ludwigia prostrate), pondweed (Potamogeton distinctus), waterwort (Elatine triandra), Chinese celery (Oenanthe javanica).
When weed killer herbicide (A) and weed killer herbicide (B) when using jointly, there be preferred super adding and (=collaborative) effect.At this, the activity of described bond is higher than the expection summation of each herbicidal activity of using.Synergy can reduce rate of application, prevent and treat more broad leaved weed, grassy weed and the sedge of wide range, the herbicide effect onset is faster, the duration is longer, just noxious plant is had better control and can widen the phase of using by only once or several times using.To a certain extent, by using said composition, also reduced harmful constituent for example nitrogen or oleic acid amount and be incorporated into amount in the soil.
Above-mentioned characteristic and advantage are avoided undesired competitive plant for putting into practice control of weeds to keep agricultural/forestry/horticultural crop or greenery patches/meadow, thereby guarantee and/or increase yield level to be necessary from the angle of quality and quantity.With regard to described characteristic, this new Herbicidal combination has surmounted the state of the art of this area significantly.
Because weeding characteristic and the plant growth regulating characteristic of Herbicidal combination of the present invention, Herbicidal combination of the present invention are used in the known plant crop or still tolerance leaved for development or genetic modification crop and contain and can prevent and treat noxious plant in the plant.Generally speaking, genetically modified plants (GMO) are characterised in that to have particularly advantageous character, except the resistance to Herbicidal combination of the present invention, for example also to plant disease or the pathogenic biology of plant disease, for example some insect or microorganism such as fungi, bacterium or virus have resistance.Other concrete feature relates to for example quantity, quality, the storage characteristics of harvested material, and the composition of specific components.Therefore, genetically modified plants known content of starch raising or that starch quality changes, or wherein harvested material has different fatty acid composition or the vitamin content that increases or the genetically modified plants of energy properties.In the same way, because its weeding and plant growth regulating character, described reactive compound also can be used for preventing and treating the crop of known plants or treats selecting noxious plant in the plant of developing and sudden change and crossbreed genetically modified plants by sudden change.
Generation is compared the conventional method with the new plant that improves characteristic and is comprised for example traditional breeding method and generation mutant with existing plant.Perhaps, have the new plant that improves character can produce by means of recombination method (referring to, for example EP-A-0221044, EP-A-0131624).Following method has for example been described in some versions:
● for starch synthetic in the plant is carried out modification, modify crop plants (for example WO92/11376, WO92/14827, WO91/19806) by means of recombinant technique
● the genetically modified crops plant, its to weed killer herbicide for example sulfonylureas present resistance (EP-A-0257993, US-A-5013659)
● have the genetically modified crops plant of the ability of generation bacillus thuringiensis (Bacillus thuringiensis) toxin (Bt. toxin), it makes plant have resistance (EP-A-0142924, EP-A-0193259) to some insect
● have the genetically modified crops plant (WO91/13972) of the fatty acid composition of change
A large amount of molecular biotechnologies is known in principle, can produce by means of these methods to have the new genetically modified plants of improving characteristic; Referring to, Sambrook et al. for example, 1989, Molecular Cloning, A Laboratory Manual, 2 NdEdition, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY; Or Winnacker " Gene und Klone ", VCH Weinheim2 NdEdition1996 or Christou, " Trends in PlantScience " 1 (1996) 423-431).In order to implement this reorganization operation, can will allow the nucleic acid molecules of sudden change or sequence variation to introduce plasmid by the dna sequence dna reorganization.For example, above-mentioned standard method allows to take place the base exchange, sequence removes, and perhaps adds natural or synthetic sequence.For dna fragmentation is interconnected, joint or conjugant can be added to these fragments.
For example, generation with the plant cell that reduces active gene prod can perhaps realize by expressing at least a ribozyme that cuts off the appropriate structuring of transcribing of said gene product specifically by expressing at least a corresponding antisense RNA, a kind of realization inhibiting just RNA altogether.
For this reason, can use the whole coded sequences that comprise gene prod, the dna molecular that comprises any side group sequence that may exist, and the dna molecular that only comprises the part coded sequence, these parts must long enough in cell, to have the antisense effect.Also can use with the coded sequence height homology of gene prod but and the DNA that not exclusively is equal to it.
When at the plant interior expression nucleic acid molecules, synthetic protein can be arranged in any required chamber of plant cell.Yet, in order to be implemented in the location in the particular chamber, coding region is connected with the dna sequence dna of guaranteeing to locate in particular chamber.This sequence is that well known by persons skilled in the art (referring to, Braun et al. for example, EMBO is (1992) J.11,3219-3227; Wolter et al., Proc.Natl.Acad.Sci.USA85 (1988), 846-850; Sonnewald et al., Plant is (1991) J.1,95-106).
Put in order the strain plant by the renewable transgenic plant cells of known technology to grow up to.In principle, genetically modified plants can be the plants of arbitrarily required plant variety,, monocotyledon are arranged not only that is, also have dicotyledon.Therefore, can express, check or the expression of inhibition or allos (=external) gene or gene order obtains the genetically modified plants that character changes by the mistake of homology (=natural) gene or gene order.
The present invention also provides selectivity to prevent and treat the method for undesired plant, preferably in crop plants, the undesired plant of control in the rice crops (under dry land or paddy field condition with indica type or round-grained rice type kind and/or rice that crossbreed/mutant/the GMO kind is planted or sowed) particularly, this method comprises component (A) and weed killer herbicide (B) as Herbicidal combination of the present invention, for example be applied to plant (noxious plant for example together or respectively, as unifacial leaf or dicotyledonous broad leaved weed, grassy weed, sedge or undesired crop plants), seed (caryopsis for example, seed or vegetative propagation organ, for example stem tuber and the band bud branch portion), perhaps be applied to the zone (for example Zai Pei zone, its also available water covering) of plant growth.A kind of weed killer herbicide can be before another kind of weed killer herbicide, be applied to plant afterwards or with it simultaneously, the zone (for example Zai Pei zone) of seed or plant growth.
Undesired plant is interpreted as meaning all plants that are grown in the place of not wanting its growth.These can be, for example, noxious plant (for example unifacial leaf or broadleaf weed, grassy weed, sedge or undesired crop plants) for example comprises those plants that some weeding active compound (for example glyphosate, Glufosinate, atrazine, imidazolinone herbicide, sulfonylurea, (mixing) aryloxy aromatic yloxy yl alkyl carboxylic acid or-Phenoxyalkylcarboxylacid acid (" fops "), cyclohexanedione oxime (" dims ") or auximone inhibitor) is had resistance.
Herbicidal combination of the present invention optionally is used for the undesired plant of following plant control, for example crop plants is such as crops, unifacial leaf crops for example, as cereal (wheat for example, barley, rye, oat, rice, corn, broomcorn millet), or dicotyledonous crops, sugar beet for example, sugarcane, rape, cotton, sunflower and leguminous plant, for example Glycine is (as soybean (Glycine max.), non-transgenic soybean (conventional cultivation kind for example for example, as the STS cultivated species) or genetically engineered soybean (for example RR soybean or LL soybean) and crossbreed thereof), Phaseolus (Phaseolus), Pisum (Pisum), Vetch (Vicia) and Arachis (Arachis), or the vegetable crop of various botany classifications, for example potato, leek, cabbage, carrot, tomato, onion; In the fruit plantation in (plantation crops), greenery patches, lawn and the pastoral area; Perhaps on non-crop zone (for example square of residential area or industrial area, railroad track), particularly in the rice crops (under dry land or paddy field condition with the indica type or plantation of round-grained rice type kind and crossbreed/mutant/GMO or the rice of sowing).Preferably both before germinateing, also the noxious plant (for example broad leaved weed, grassy weed, sedge or undesired crop plants) that has germinateed was used noxious plant, and irrelevant with the vegetative period of the crop of sowing/planting.
The present invention also provides Herbicidal combination of the present invention to be used for the purposes that selectivity is prevented and treated undesired plant, preferably in crop plants, particularly prevent and treat undesired plant in the rice crops (under dry land or paddy field condition with the indica type or plantation of round-grained rice type kind and crossbreed/mutant/GMO or the rice of sowing).
If Herbicidal combination of the present invention can be formulated as for example single component by known method---suitable, with other reactive compound, additive and/or common dosage forms auxiliary agent---mix preparation, then this bond is used behind the dilute with water in a usual manner; Perhaps be formulated as a barrel mix formulation by the common dilution of each the component water that will prepare separately or part is prepared separately.All right separate administration is preparation or independent each component prepared of part separately.Also can divide many parts to use described weed killer herbicide or Herbicidal combination (sequential application), before for example at first seed dressing is used or is sowed/then carry out after using before plantation pre-treatment or the bud using behind the bud or early stage bud after use, carry out then using behind mid-term or the later stage bud.This preferred common reactive compound that uses or almost use described bond simultaneously, preferred especially common the use.
Described weed killer herbicide (A) and (B) can be jointly or be converted into conventional formulation respectively, for example solution, emulsion, suspending agent, pulvis, foaming agent, paste, granule, aerosol, with the microcapsules in natural and synthetic material and the polymeric material of reactive compound dipping.Also can mention being specifically designed to the preparation of cultivating rice, for example use disseminating with granule, especially big granule, floating particle agent, floating suspension emulsion by paddy field water either dissolving and distribution again by shaking bottle.Described preparation can comprise conventional auxiliary agent and additive.
Prepare these preparations in known manner, for example by mixing, randomly use surfactant (being emulsifier and/or dispersant) and/or blowing agent to prepare described reactive compound and filler (being liquid flux, pressurized liquefied gas and/or solid carrier).
If used filler is water, for example also can use organic solvent as secondary solvent.Main suitable liquid flux is: aromatic compounds, for example dimethylbenzene, toluene or Fluhyzon; Chlorinated aromatic hydrocarbons and chloro aliphatic hydrocarbon, for example chlorobenzene, vinyl chloride or carrene; Aliphatic hydrocarbon, for example cyclohexane or paraffin are as mineral oil fractions, mineral oil and vegetable oil; Alcohols, for example butanols or ethylene glycol and ether thereof and ester; Ketone, for example acetone, methyl ethyl ketone, methyl iso-butyl ketone (MIBK) or cyclohexanone; Intensive polar solvent, for example dimethyl formamide and dimethyl sulfoxide (DMSO), and water.
Suitable solid carrier is: for example natural minerals of ammonium salt and pulverizing, for example kaolin, clay, talcum, chalk, quartz, attapulgite, montmorillonite or diatomite; With the synthetic mineral of pulverizing, for example high dispersive silica, aluminium oxide and silicate; The solid carrier that is applicable to granule is: for example pulverize the also natural crystal of classification, for example calcite, marble, float stone, sepiolite and dolomite, and the synthetic particle of inorganic and organic powder, and the particle of organic material (for example sawdust, coconut husk, corncob and tobacco rods); Suitable emulsifier and/or blowing agent are: for example nonionic and anion emulsifier, for example polyoxyethylene fatty acid ester, polyoxyethylene fatty alcohol ether, for example alkylaryl polyglycol ether, alkylsulfonate, alkyl sulfate, arylsulphonate, and protein hydrolysate; Suitable dispersant is: for example lignin sulfite waste liquor and methylcellulose.
Can use tackifier, for example carboxymethyl cellulose in the described preparation; Natural and the synthetic polymer of powder, particle or latex form, for example gum Arabic, polyvinyl alcohol and polyvinyl acetate; And natural phospholipid, for example cephalin and lecithin and synthetic phospholipid.Other possible additives are mineral oil and vegetable oil.
The herbicide effect of Herbicidal combination of the present invention can improve by following material, for example by surfactant, preferably by being selected from the wetting agent of fatty alcohol polyglycol ether.Described fatty alcohol polyglycol ether preferably comprises 10-18 carbon atom, comprises 2-20 ethylene oxide,1,2-epoxyethane base unit in the polyethylene glycol ether moiety in the fatty alcohol group.Fatty alcohol polyglycol ether can non-ionic form or ionic species the form of fatty alcohol polyglycol ether sulphate---for example with---and exist, it for example can be used as alkali metal salt (for example sodium salt and sylvite) or ammonium salt or even uses C for example as alkali salt (for example magnesium salts) 12/ C 14Fatty alcohol diethylene glycol (DEG) ether sodium sulfate (
Figure BDA00003397318800231
Clariant GmbH); Referring to, for example EP-A-0476555, EP-A-0048436, EP-A-0336151 or US-A-4,400,196 and Proc.EWRS Symp. " Factors Affecting Herbicidal Activity and Selectivity ", 227-232 (1988).The nonionic fatty alcohols polyglycol ether is, for example, and (C 10-C 18), preferred (C 10-C 14) fatty alcohol polyglycol ether (for example different tridecanol polyglycol ether), it for example comprises 2-20,3-15 ethylene oxide,1,2-epoxyethane base unit preferably, for example is selected from
Figure BDA00003397318800232
Those of series, for example
Figure BDA00003397318800233
Or
Figure BDA00003397318800235
(all available from Clariant GmbH).
The present invention comprises component (A) and component (B) and the above-mentioned bond that is selected from the wetting agent of fatty alcohol polyglycol ether again, described fatty alcohol polyglycol ether preferably comprises 10-18 carbon atom and comprises 2-20 ethylene oxide,1,2-epoxyethane base unit at the polyethylene glycol ether moiety in the fatty alcohol group, and it can be with nonionic or ionic species (for example fatty alcohol polyglycol ether sulphate) and exist.Preferred C 12/ C 14Fatty alcohol diethylene glycol (DEG) ether sodium sulfate (
Figure BDA00003397318800236
Clariant GmbH) and contain the different tridecanol polyglycol ether of 3-15 ethylene oxide,1,2-epoxyethane base unit, for example be selected from
Figure BDA00003397318800237
Series, for example
Figure BDA00003397318800238
With
Figure BDA00003397318800239
(all available from Clariant GmbH).
In addition, known fatty alcohol polyglycol ether, for example nonionic or ionic fatty alcohol polyglycol ether (for example fatty alcohol polyglycol ether sulphate), also be suitable for use as the bleeding agent of multiple other weed killer herbicides and active reinforcing agent (referring to, for example, EP-A-0502014).Therefore, the present invention also comprises the bond with suitable bleeding agent and active reinforcing agent (preferably with its commercial form).
Herbicidal combination of the present invention also can use with vegetable oil.The term vegetable oil is interpreted as meaning the oil of oil-produced vegetable kind, for example soybean oil, rapeseed oil, corn oil, sunflower oil, cotton seed oil, linseed oil, cocoa butter, palm oil, Ji oil or castor oil, rapeseed oil particularly, and ester exchange offspring, Arrcostab for example is as rapeseed oil methyl ester or rapeseed oil ethyl ester.
Vegetable oil is preferably C 10-C 22, preferred C 12-C 20The ester of fatty acid.Described C 10-C 22Fatty acid ester is, for example unsaturated or saturated C 10-C 22Fatty acid particularly contains those of even number of carbon atoms, for example erucic acid, dodecylic acid, hexadecanoic acid, particularly C 18Fatty acid, for example stearic acid, oleic acid, linoleic acid or linolenic acid.
C 10-C 22The example of fatty acid ester is contained C in the oil that passes through glycerine or ethylene glycol and for example oil-produced vegetable kind 10-C 22The ester of fatty acid response gained perhaps is can be by for example above-mentioned glycerine or ethylene glycol C 10-C 22Fatty acid ester and C 1-C 20Alcohol (for example methyl alcohol, ethanol, propyl alcohol or butanols) ester exchange and the C that obtains 1-C 20Alkyl-C 10-C 22Fatty acid ester.Ester exchange can for example be passed through
Figure BDA000033973188002411
Chemie Lexikon, 9th edition, Volume2, page1343, the known method of describing among the Thieme Verlag Stuttgartz carries out.
Preferred C 1-C 20Alkyl-C 10-C 22Fatty acid ester is methyl esters, ethyl ester, propyl ester, butyl ester, 2-ethylhexyl and dodecane ester.Preferred ethylene glycol-C 10-C 22Fatty acid ester and glycerine-C 10-C 22Fatty acid ester is C single or that mix 10-C 22The glycol ester of fatty acid and glycerine ester, described fatty acid particularly contains the fatty acid of even number of carbon atoms, for example erucic acid, dodecylic acid, hexadecanoic acid, particularly C 18Fatty acid, for example stearic acid, oleic acid, linoleic acid or linolenic acid.
In Herbicidal combinations of the present invention, the vegetable oil for example form of commercially available oil-including formulation additive exists, particularly based on those of rapeseed oil, for example
Figure BDA00003397318800241
(Victorian Chemical Company, Australia hereinafter is called Hasten, main component: the rapeseed oil ethyl ester),
Figure BDA00003397318800242
(Novance, France hereinafter are called ActirobB, main component: rapeseed oil methyl ester),
Figure BDA00003397318800243
(Bayer AG, Germany hereinafter are called Rako-Binol, main component: rapeseed oil),
Figure BDA00003397318800244
(Stefes, Germany hereinafter are called Renol, the vegetable oil composition: rapeseed oil methyl ester) or
Figure BDA00003397318800245
(Stefes, Germany hereinafter are called Mero, main component: rapeseed oil methyl ester).
In another embodiment, the present invention also comprises the bond that contains above-mentioned vegetable oil, described vegetable oil for example rapeseed oil, preferably with the form of commercially available oil-including formulation additive, particularly based on those of rapeseed oil, for example
Figure BDA00003397318800246
(Victorian Chemical Company, Australia hereinafter is called Hasten, main component: the rapeseed oil ethyl ester),
Figure BDA00003397318800247
(Novance, France hereinafter are called ActirobB, main component: rapeseed oil methyl ester), (Bayer AG, Germany hereinafter are called Rako-Binol, main component: rapeseed oil), (Stefes, Germany hereinafter are called Renol, the vegetable oil composition: rapeseed oil methyl ester) or
Figure BDA000033973188002410
(Stefes, Germany hereinafter are called Mero, main component: rapeseed oil methyl ester).
Can use colouring agent, inorganic pigment for example is as iron oxide, titanium oxide and Prussian blue; And toner, for example alizarin colouring agent, azo colouring agent and metal phthalocyanine colouring agent; And micronutrient, for example molysite, manganese salt, boron salt, mantoquita, cobalt salt, molybdenum salt and zinc salt.
Usually, described preparation comprises the reactive compound of 0.1 to 95 weight %, preferred 0.5 to 90 weight %.
Weed killer herbicide (A) and (B) also can be used for the undesired plant of control with itself or as the dosage form that mixes with other agricultural chemical activity compounds (for example known weed killer herbicide), for example be used for controlling weeds or be used for the undesired crop plants of control, also can be for example finished product preparation or the mixed thing of bucket.
Also can mix with other known reactive compound, described other known reactive compound is the reagent of fungicide, insecticide, miticide, nematocide, safener, bird repellent, nutrient for plants and the structure of improving the soil for example.
Weed killer herbicide (A) and (B) can itself, its dosage form or by further dilution and type of service prepared therefrom uses, for example ready to use solution, suspending agent, emulsion, pulvis, paste and granule.Available usual manner---for example by watering, spray, atomize or broadcasting sowing---uses them.
Described reactive compound can be applied to plant (noxious plant for example, for example unifacial leaf or dicotyledonous broad leaved weed, grassy weed, sedge or undesired crop plants), seed (for example caryopsis, seed or vegetative propagation organ, the branch portion of stem tuber or band bud for example) or cultural area (for example soil), preferably be applied to green plants and plant parts and, if suitable, additionally be applied to soil.A kind of possible use is to use described reactive compound jointly with the form of the mixed thing of bucket, and wherein the concentrate formulation that the best of each reactive compound is prepared mixes in groove with water, uses the gained flushing liquor then.
Weed killer herbicide (A) and the associating herbicidal formulations according to bond of the present invention (B) have more wield advantage, because the amount of described component has been optimal proportion.In addition, the auxiliary agent in the preparation can be regulated each other and optimize.
Biology embodiment
Act on behind the bud of weeding
Method
Seed or the rhizome of unifacial leaf and dicotyledonous harmful plants and useful plant are placed the peat basin (diameter 4cm) that sandy loam is housed, cover with soil then.The peat basin remains in the greenhouse under optimum condition.In addition, the noxious plant that runs in the rice cultivating is cultivated in the peat basin, and made the water surface than the high 2cm of soil surface.
Cultivate beginning about 3 weeks of back, handle test plants in 1 leaf phase leaf phase to 3.Weed killer herbicide---is formulated into the component (A) of suspension emulsion (SC) and is formulated into the component (B) of wetting powder (WP)---separately or with the form of bond of the present invention, be sprayed at the green parts of plant with various dose with the rate of application of 600l water/hectare (scaled value).In order further to cultivate plants, subsequently the peat basin is remained in the greenhouse under optimum condition.
The visual score of herbicidal effect was up to after handling under time interval of 21 days to be carried out.Scoring is to carry out with the percentage of comparing with untreated check plant.0%=does not have activity of weeding, and 100%=is activity of weeding=kill fully completely.
Use weed killer herbicide (=single using) processing and calculate interaction with the percentage that bond of the present invention (=mixture) is handled with independent with the Colby method.When the effectiveness of observed mixture exceed that the single form of using test value adds and the time, it has also surpassed the desired value according to Colby, the desired value of Colby is calculated (referring to S.R.Colby with following formula; Weeds15 (1967) 20-22):
E=A+B-(A?x?B/100)
This:
A, B=component A and B respectively when dosage is a g ai/ha (=g active substance/hectare) and b g ai/ha in the activity of percentage.
E=when dosage is a+b g ai/ha in the desired value of percentage.
The result
According to weed killer herbicide of the present invention (A) and bond (B) important noxious plant (grassy weed at following wide spectrum, broad leaved weed/sedge) and useful plant test: common wheat (Triticum aestivum (TRZAS)), chickweed (Stellaria media (STEME)), Annual Ryegrass (Lolium multiflorum (LOLMU)), Arabic Veronica (Veronica Persica (VERPE)), big fringe amur foxtail (Alopecurus myosuroides (ALOMY)), scentless mayweed (Matricaria inodora (MATIN)), colea (Brassica napus (BRSNW)), pansy (Viola tricolor (VIOTR)), wild oat (Avena fatua (AVEFA)), Amaranthus retroflexus (Amaranthus retroflexus (AMARE)), corn (Zea mays) (ZEAMX), Pharbitis purpurea (Pharbitis purpurea (PHBPU)), green foxtail (Setaria viridis (SETVI)), volume stem knotweed (Fallopia (ex Polygonum) Convolvulus (POLCO)), barnyard grass grass (Echinochloa crusgalli (ECHCG)), piemarker (Abuthilon theophrasti (ABUTH)), oil Sha's beans (Cyperus esculentus (CYPES)), rice (Oryza sativa (ORYSA)).
Particularly advantageous is the result shown in the following table, has wherein used following keyword:
(1) EPPO of treated plant coding (aforementioned Bayer coding) (seeing above)
(2) scoring time: DAT (fate after the processing)
(3) fractions tested A (identification code)
(4) fractions tested B (identification code)
(5) dosage of component A [g ai/ha]
(6) dosage of B component [g ai/ha]
(7) Shi Ce active %
(8) E value (calculating according to Colby: see above)
(9) note: " SYNERGY "=cooperative interaction (the active % of E value<actual measurement); " SAFENING "=to the safener effect (the active % of E value>actual measurement) of useful plant
Figure BDA00003397318800271
Figure BDA00003397318800281
Figure BDA00003397318800291

Claims (6)

1. comprise component (A) and Herbicidal combination (B), wherein
(A) compound described by formula (A) of expression:
Figure FDA00003397318700011
And
(B) compound described by formula (B) of expression:
Figure FDA00003397318700012
2. the Herbicidal combination of claim 1, wherein component (A) and (B) weight ratio (A): (B) usually 1: 1500 to 500: 1, preferred 1: 1000 to 100: 1, particularly in 1: 200 to 20: 1 the scope.
3. claim 1 or 2 Herbicidal combination, its comprise the component (A) of effective dose and (B) and/or extra one or more be selected from other following component: dissimilar agrochemically active compounds, the formulation auxiliary agents that is usually used in crop protection and additive.
4. prevent and treat the method for undesired plant, wherein will be according to the component (A) of the Herbicidal combination of in the claim 1 to 3 or multinomial definition and (B) be applied to noxious plant, its seed or vegetative propagation organ or the zone of these plants growths jointly or individually.
5. the method for claim 4 is used at crop plants---for example wheat, corn, soybean, sugar beet, sugarcane, cotton, rice, beans, flax, barley, oat, rye, triticale, rape, potato, broomcorn millet, herbage, greenery patches/lawn---, the undesired plant of control in the fruit plantation or in non-crop zone, the particularly rice crops.
6. the Herbicidal combination of each definition is used for the purposes of the undesired plant of control in the claim 1 to 3.
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