synergistic herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-met

专利摘要:
summary of the invention patent: "herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof -toxy-pyrimidine and its derivatives ". the present invention relates to a synergistic herbicidal composition containing (a) a compound of formula (i): or its agriculturally acceptable salt or ester and (b) dimethoxy-pyrimidine acids, including, but not limited to, bispiribac -sodium, piriben-zoxim, pyriftalid, piriminobac-methyl and pyrimisulfan provides synergistic control of undesirable vegetation, for example, in rice directly sown, sown in water and transplanted, cereals, wheat, barley, oats, rye, sorghum, corn , sugar cane, sunflower, rapeseed, canola, beet, soybeans, pineapple, vegetables, pastures, lawns, pastures, fallow, grass, tree and vineyard orchards, aquatic, plantation crops, vegetation control industrial (ivm) or rights of way (row).
公开号:BR102013018526B1
申请号:R102013018526
申请日:2013-07-19
公开日:2020-02-04
发明作者:Yerkes Carla；Mann Richard
申请人:Dow Agrosciences Llc；
IPC主号:

专利说明:

Invention Patent Descriptive Report for SYNERGIC HERBICIDIC COMPOSITIONS UNDERSTANDING ACID 4 AMINO-3-CHLORO-5-FLUORO-6- (4-CHLORINE-2-FLUORO-3-METOXYphenyl) PYRIDINE-2-CARBOXYLIC OR BUTY OR BENZIL IS STERILE SAME AND A DIMETHOXY-PYRIMIDINE AND ITS DERIVATIVES, AND METHOD FOR UNDESIRABLE VEGETATION CONTROL.
Priority Claim [001] This application claims the benefit of U.S. provisional patent applications number 61 / 675,109, filed on July 24, 2012, and 61 / 675,117, filed on July 24, 2012, and patent application US utility model number 13 / 833,362, filed on March 15, 2013, all of these requests being incorporated by reference in their entirety.
Field [002] Herbicidal compositions are presented here comprising (a) 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3methoxyphenyl) pyridine-2-carboxylic acid or its ester or salt agriculturally acceptable and (b) a dimethoxy-pyrimidine, such as a pyrimidinyloxybenzoic acid or a pyrimidinylthiobenzoic acid or its agriculturally acceptable salt or ester.
[003] Undesirable vegetation control methods including the application of (a) 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2- are also presented here carboxylic acid or its agriculturally acceptable ester or salt and (b) a dimethoxypyrimidine, such as pyrimidinyloxybenzoic acids or pyrimidinylthiobenzoic acids or their agriculturally acceptable salts or esters.
Background [004] The protection of crops against weeds and other vegetation that inhibits crop growth is a constantly recurring problem in agriculture. To help combat this problem, researchers in the field of synthetic chemistry have produced
Follows on sheet 1a / 69
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1a / 69
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2/69 chemicals of many types have been reported in the literature, and a large number are in commercial use. However, there is still a need for compositions and methods that are effective in controlling undesirable vegetation.
Summary [005] A first embodiment of the invention presented herein includes herbicidal compositions comprising a herbicidally effective amount of (a) a compound of Formula (I)
or its agriculturally acceptable salt or ester, and (b) at least one dimethoxy-pyrimidine selected from the group consisting of: pyrimidinyloxybenzoic acids, pyrimidinylthiobenzoic acids, and their agriculturally acceptable salts and esters.
[006] A second modality includes mixing the first modality, in which Formula (I) is present in the form of at least one of the following forms: a carboxylic acid, a carboxylate salt, an aralkyl, an alkyl ester, a non-benzyl substituted, a substituted benzyl, a C1-C4 alkyl and / or an n-butyl ester.
[007] A third modality includes the mixture according to the first or the second modality, in which (b) at least one dimethoxy-pyrimidine selected from the group consisting of: bispyribacsodium, pyribenzoxim, pyriftalid, pyriminobac-methyl or pyrimisulfan, or its salt, carboxylic acid, carboxylate salt or agriculturally acceptable ester of at least one of the aforementioned dimethoxy-pyrimidines.
[008] A fourth modality includes mixtures according to any one of the first, second or third modalities, in which the
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3/69 dimethoxy-pyrimidine in the mixture is bispyribac-sodium, where the weight ratio of the compound of Formula (I) to bispyribac-sodium, given in units of gae / ha to gai / ha or gae / ha to gae / ha , is selected from the group of ratios and ratios that consists of about: 1:75 to 43: 1, 1: 0.8, 1: 0.4, 1: 1.6, 1: 1.4, 1 : 0.6, 1: 0.3, 1: 2.3, 1: 3, 1: 1.1, 1: 4.6, 1.75: 1, 2.5: 1, 5; 1, 1 : 70 to 40: 1, 1:60 to 30: 1, 1:50 to 20: 1, 1:40 to 15: 1, 1:30 to 10; 1, 1:20 to 5: 1, 1:10 to 4: 1, 1: 5 to 1: 1 and 10: 1 to 1: 9, or within any defined range between any pair of previous values. [009] A fifth embodiment includes mixtures according to any of the first, second or third embodiments, wherein the dimethoxy-pyrimidine in the mixture is pyribenzoxim, wherein the weight ratio of the compound of Formula (I) to pyribenzoxim, given in units from gae / ha to gai / ha or gae / ha to gae / ha, it is selected from the group of ratios of ratios and ratios consisting of about: 1:45 to 10: 1, 1: 8,8, 1 : 4.4, 1: 2.2, 1:40 to 9: 1, 1:30 to 7: 1, 1:20 to 5: 1, 1:10 to 4: 1 and 1: 9 and 1:45 , or within any defined range between any pair of preceding values.
[0010] A sixth modality includes mixtures according to any one of the first, second or third modalities, in which the dimethoxy-pyrimidine in the mixture is pyriftalid, in which the weight ratio of the compound of Formula (I) to pyriftalid, given in units of gae / ha to gai / ha or gae / ha to gae / ha, it is selected from the group of ratios of ratios and ratios consisting of about: 1: 150 to 3: 1, 1:10, 1:21 , 1: 2,6, 1: 5,2, 1: 2,5, 1:10, 1: 20,1: 26, 1: 10,3, 1: 6, 1: 100 to 2.5: 1 , 1:75 to 2: 1, 1:50 to 1.5: 1, 1:30 to 1: 1 and 1:21 to 0.75: 1, or within any defined range between any pair of previous values.
[0011] A seventh embodiment includes mixtures according to any of the first, second or third embodiments, wherein the dimethoxy-pyrimidine in the mixture is pyriminobac-methyl, wherein the weight ratio of the compound of Formula (I) to pyriminobac -methyl, given in uni
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4/69 from gae / ha to gai / ha or gae / ha to gae / ha, is selected from the group of ratios of ratios and ratios consisting of about: 1:45 to 27: 1, 1: 9, 1 : 4.4, 1:40 to 25: 1, 1:30 to 20: 1, 1:20 to 10: 1, 1:10 to 5: 1 and 1:21 to 6: 1, or within any range defined between any pair of preceding values.
[0012] An eighth embodiment includes mixtures according to any of the first, second or third embodiments, wherein the dimethoxy-pyrimidine in the mixture is pyrimisulfan, wherein the weight ratio of the compound of Formula (I) to pyrimisulfan, given in units from gae / ha to gai / ha or gae / ha to gae / ha, it is selected from the group of ratios of ratios and ratios consisting of about: 1: 100 to 30: 1, 1:70 to 25: 1 , 1:50 to 22: 1, 1:20 to 20: 1, 1:10 to 10: 1, 1: 7 to 7: 1 and 1: 5 to 5: 1, or within any defined range between any pair previous values.
[0013] A ninth modality includes any composition according to any one of the first to eighth modalities, wherein the mixture also comprises at least one agriculturally acceptable agent selected from the group consisting of an adjuvant, a vehicle or a protector.
[0014] A tenth modality includes methods of controlling undesirable vegetation comprising the stages of application or other contact of vegetation and / or soil and / or water with a herbicidally effective amount of at least one mixture according to any of the first to the ninth modalities.
[0015] An eleventh modality includes methods according to the eleventh modality, in which undesirable vegetation is controlled by the practice of at least one of the methods in at least one member of the group consisting of: rice directly sown, sown in water and / or transplanted, cereals, wheat, barley, oats, rye, sorghum, corn, sugar cane, sunflower, rapeseed, canola, beet,
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5/69 soybeans, cotton, pineapple, pastures, lawns, pasture, fallow, grass, tree and vineyard orchards, aquatic, plantation crops, vegetables, industrial vegetation control (IVM) or rights of way (ROW).
[0016] A twelfth modality includes methods according to the tenth and eleventh modalities, in which a herbicidally effective amount of the mixture is applied in pre- or post-emergence to at least one of the following: a crop, a field, a ROW or a rice field.
[0017] A thirteenth modality includes methods according to any one of the tenth to twelfth modalities, in which undesirable vegetation can be controlled by practicing at least one of the methods on at least one plant that is resistant or tolerant to the members of the system. group consisting of: glyphosate, 5-enolpyruvylshikimato-3-phosphate (EPSP) synthetase inhibitor, glufosinate, glutamine synthetase inhibitor, dicamba, phenoxy auxin, auxin pyridyloxy, synthetic auxin, auxin transport inhibitor, aryloxyphenoxypropionate, phenyloxypropionate, aryloxyphenoxypropionate, , acetyl CoA carboxylase (ACCase) inhibitor, imidazolinone, sulfonylurea, pyrimidinylthiobenzoate, triazolopyrimidine, sulfonylaminocarbonyltriazolinone, acetolactate synthase (ALS) inhibitor or acetohydroxy acid synthetase (AHAS), pyridine-hydroxide inhibitor desaturase, carotenoid biosynthesis inhibitor, protoporphyrinogen ox inhibitor idase (PPO), cellulose biosynthesis inhibitor, mitosis inhibitor, microtubule inhibitor, very long chain fatty acid inhibitor, fatty acid and lipid biosynthesis inhibitor, photosystem I inhibitor, photosystem II inhibitor, protoporphyrinogen inhibitor oxidase (PPO), triazine and bromoxynil.
[0018] A fourteenth modality includes at least one method according to any one of the fourteenth to the thirteenth mo
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6/69 dalities, where a plant is resistant or tolerant to at least one herbicide, and where the resistant or tolerant crop has multiple or stacked traits that confer tolerance to multiple herbicides or inhibitors of multiple modes of herbicidal action, in some modalities, the treated plant that expresses resistance to a herbicide is itself an undesirable vegetation.
[0019] A fifteenth modality includes methods according to the fourteenth modality, in which the resistant or tolerant weed is a biotype with resistance or tolerance to multiple herbicides, multiple chemical classes, inhibitors of multiple modes of herbicidal action or by multiple resistance mechanisms.
[0020] A sixteenth modality includes at least one of the methods according to the fourteenth or fifteenth modality, in which the resistant or tolerant undesirable plant is a resistant biotype or tolerant to at least one or more compounds that act according to at least one mode of action selected from the group consisting of: acetolactate synthase (ALS) inhibitors or acetohydroxy acid synthase (AHAS), photosystem II inhibitors, acetyl CoA carboxylase (ACCase) inhibitors, synthetic auxins, auxin transport inhibitors , photosystem I inhibitors, 5enolpyruvilshikimato-3-phosphate (EPSP) synthetase inhibitors, microtubule assembly inhibitors, fatty acid and lipid synthesis inhibitors, protoporphyrinogen oxidase (PPO) inhibitors, carotenoid biosynthesis inhibitors, acid inhibitors very long-chain fatty acids (VLCFA), phytoene desaturase (PDS) inhibitors, glutamine synthetase inhibitors, 4 -hydroxyphenylpyruvate dioxigenase (HPPD), mitosis inhibitors, cellulose biosynthesis inhibitors, herbicides with multiple modes of action, quinclorac, arylaminopropionic acids, difenzoquat, endothal or organoarsenic.
[0021] A seventeenth modality includes methods of control
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7/69 of undesirable vegetation comprising the step of applying a herbicidally effective amount of at least one mixture according to the fourth modality, in which the amount of the mixture is applied at a rate, expressed in gai / ha or gae / ha of bispiribac-sodium selected from the group of rates and rate ranges consisting of about: 1, 5, 7, 10, 14, 20, 40, 70, 80 and 100, or within any defined range between any pair of the preceding values .
[0022] An eighteenth modality includes methods according to the fourth and sixteenth modalities, in which the controlled plant is at least one plant selected from the group consisting of: LEFCH, ECHCG, ECHOR, SCPMA and CYPRO, yet other modalities include the control of plants of the genera that consist of: Leptochloa, Echinochloa, Bolboschoenus and Cyperus.
[0023] A nineteenth modality includes methods of controlling undesirable vegetation comprising the step of applying a herbicidally effective amount of at least one mixture according to the fifth modality, in which the amount of the mixture is applied at a rate, expressed in pyribenzoxim gai / ha or gae / ha, selected from the group of rates and rate ranges consisting of about: 70, 15 to 60 and 2 to 300, or within any range defined between any pair of the preceding values.
[0024] A twentieth modality includes methods according to the fifth and nineteenth modalities, in which the controlled plant is at least one plant selected from the group consisting of: ECHCG, yet other modalities include the control of plants of the genera consisting of : Echinochloa.
[0025] A twenty-first modality includes methods of controlling undesirable vegetation comprising the step of applying a herbicidally effective amount of at least one mixture according to the sixth modality, wherein the amount of the mixture is
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8/69 applied to a rate, expressed in gai / ha or gae / ha of pyriftalid, selected from the group of rates and rate ranges consisting of about: 1: 150 to 3: 1, 1: 10,3, 1 : 21, 1: 2,6, 1: 5,2, 1: 2.5 and 1:21 to 0,75: 1, or within any defined range between any pair of previous values. [0026] A twenty-second modality includes methods according to the sixth and twenty-second modalities, in which the controlled plant is at least one plant selected from the group consisting of: BRAPP, LEFCH, CYPRO and FIMMI, yet other modalities include control of plants of the genera consisting of: Leptochloa, Cyperus, Fimbristylis and Brachiaria.
[0027] A twenty-third modality includes methods of controlling undesirable vegetation comprising the step of applying a herbicidally effective amount of at least one mixture according to the seventh modality, in which the amount of the mixture is applied at a rate, expressed in gai / ha or gae / ha, of piriminobacmetil selected from the group of rates and rate ranges consisting of about: 1:45 to 27: 1, 5.5, 11.25, 22.5, 45, 90, 180 and 1:21 to 6: 1 or within any defined range between any pair of preceding values.
[0028] A twenty-fourth modality includes methods according to the seventh and twenty-third modalities, in which the controlled plant is at least one plant selected from the group consisting of: DIGSA, IPOHE, LEFCH, ECHCO, FIMMI, SCPMA and CYPRO, still other modalities include the control of plants of the genera that consist of: Digitaria, Ipomoea, Leptochloa, Echinochloa, Fimbristylis, Bolboschoenus and Cyperus.
[0029] A twenty-fifth modality includes methods of controlling undesirable vegetation comprising the step of applying a herbicidally effective amount of at least one mixture according to the seventh modality, wherein the amount of the mixture is
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9/69 applied to a rate, expressed in gai / ha or gae / ha, of pirimisulfan selected from the group of rates and rate ranges consisting of about: 5, 20, 50, 100, 150, 200 and 300, or within any defined range between any pair of preceding values.
[0030] A twenty-sixth modality includes methods according to the seventh and twenty-fifth modalities, in which the controlled plant is at least one plant selected from the group consisting of: CYPRO, ECHCG, ECHCO, LEFCH, SCPMA, DIGSA, IPOHE and FIMMI, still other modalities include the control of plants of the genera that consist of: Cyperus, Digitaria, Echinochloa, Fimbristylis, Ipomoea, Leptochloa, Schoenoplectus and Bolboschoenus.
[0031] Herbicidal compositions are presented here comprising a herbicidally effective amount of (a) a compound of Formula (I)
π, - ⁰ ω or its agriculturally acceptable salt or ester, and (b) a dimethoxy-pyrimidine. The compositions can also include an agriculturally acceptable adjuvant or vehicle.
[0032] Also presented here are methods of controlling undesirable vegetation comprising the application of (a) a compound of Formula (I) or its agriculturally acceptable ester or salt and (b) an herbicide dimethoxy-pyrimidine or its agriculturally acceptable salt or ester .
Detailed Description
DEFINITIONS [0033] As used herein, the compound of Formula (I) has the sePetition 870180150139, of 11/09/2018, p. 15/86
10/69 following structure:
nh ₂
Cl
.OH (I) h ₃ c [0034] The compound of Formula (I) can be identified by the name 4-amino-3-chloro-6- (4-chloro-2-fluoro-3-methoxyphenyl) -5- fluoropyridine2-carboxylic and was described in US patent 7,314,849 (B2), which is incorporated herein by reference in its entirety. Exemplary uses of the compound of Formula (I) include the control of undesirable vegetation, including grassy, broad-leaved weeds, in multiple non-harvest and harvest situations.
[0035] Pyrimidineoxycarboxylic acids contain, in certain embodiments, the following core structure:
OH which can be substituted with one or more substituents, and their salts and esters. Phenyl and pyrimidine can independently be part of a multicyclic ring system. The oxygen connected to both pyrimidine and phenyl can be replaced by another heteroatom, for example, S. Without limitation to any theory, the compounds inhibit acetolactate synthase (ALS) or (AHAS) acetohydroxy acid synthetase (AHAS), the first common enzyme in the biosynthesis of branched chain amino acids.
Exemplary pyrimidinylthiobenzoate acids or their salts or esters include, but are not limited to, bispyribac-sodium, pyribenzoxy, pyriftalid, pyriminobac-methyl and pyrimisulfan, agriculturally acceptable derivatives, for example, carboxylic acid, carbo-salt
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11/69 xylate or its ester.
[0037] As used herein, bispiribac-sodium is 2,6-bis [(4,6-dimethoxy-2-pyrimidinyl) oxy] sodium benzoate and has the following structure:
[0038] The compound has been described in Tomlin, C., ed. A World Compendium The Pesticide Manual. 15th ed. Alton: BCPC Publications, 2009 (hereafter, “The Pesticide Manual, Fifteenth Edition, 2009.”). Exemplary uses of bispiribac-sodium include its use to control grasses, weeds and broadleaf weeds, for example, in rice sown directly and sown in water and grass.
[0039] As used herein, pyribenzoxim is diphenylmethanone O [2,6-bis [(4,6-dimethoxy-2-pyrimidinyl) oxy] benzoyl] oxime and has the following structure:
[0040] The compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of pyribenzoxim include its use for post-emergence control of colony grass, grass
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12/69 foxtail and Polygonums, for example, in rice, wheat and zoysia grass.
[0041] As used herein, pyriftalid is 7 - [(4,6-dimethoxy-2pyrimidinyl) thio] -3-methyl-1 (3H) -isobenzofuranone and has the following structure:
CH [0042] The compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of pyriftalid include its use for post-emergence control of a broad spectrum of weeds, for example, in rice.
[0043] As used herein, pyriminobac-methyl is 2 - [(4,6-dimethoxy2-pyrimidinyl) oxy] -6- [1- (methoxyimino) ethyl] benzoate and has the following structure:
/ CH
The [0044] The compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of piriminobac-methyl include its use for early post-emergence control of colony grass, for example, in rice paddies.
[0045] As used herein, pyrimisulfan is N- [2 - [(4,6-dimethoxy-2 pyrimidinyl) hydroxymethyl] -6- (methoxymethyl) phenyl] -1, 1 difluoromethanesulfonamide and has the following structure:
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13/69
[0046] Its herbicidal activity is exemplified in the Journal of Pesticide Science (Tokyo, Japan) (2012), 37 (1), 62-68. Pirimisulfan can be used, for example, as a herbicide to control rice weeds in rice fields. As used herein, herbicide means a compound, for example, an active ingredient, which kills, controls, or otherwise adversely modifies the growth of plants.
[0047] As used herein, a herbicidally effective or vegetation control amount is an amount of active ingredient that causes an adverse change in vegetation, for example, causes deviations from natural development, death, effect regulation, cause desiccation, cause delay and others.
[0048] As used herein, control of undesirable vegetation means prevention, reduction, death or other form of adverse change in the development of plants and vegetation. Methods of controlling undesirable vegetation by applying certain herbicidal combinations or compositions are described here. Application methods include, but are not limited to, applications to vegetation or its location, for example, application to the area adjacent to vegetation, as well as applications in pre-emergence, post-emergence, leaf (spreading, directed, banded, punctual , mechanical, overhead or rescue) and in water (immersed or submerged vegetation, scattering, punctual, mechanical, water injection, granular scattering, granular punctuation, agitator bottle or spraying in the water stream) using manual application methods, backpack, machine, tractor or
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Aerial 14/69 (plane and helicopter).
[0049] As used herein, plants and vegetation include, but are not limited to, germinative seeds, emerging seedlings, plants emerging from vegetative propagules, immature vegetation and established vegetation.
[0050] As used herein, agriculturally acceptable salts and esters refer to salts and esters which exhibit herbicidal activity or which are or can be converted to plants, water or soil in the herbicide in question. Exemplary agriculturally acceptable esters are those that are or can be hydrolyzed, oxidized, metabolized or otherwise converted, for example, into plants, water or soil in the corresponding carboxylic acid which, depending on the pH, can be in dissociated or non-dissociated form.
[0051] Exemplary salts include those derived from alkali or alkaline earth metals and those derived from ammonia and amines. Exemplary cations include sodium, potassium, magnesium and amine cations of Formula:
R1R ² R ³ R ⁴ N ⁺ [0052] where R ¹ , R ² , R ³ and R ⁴ , each independently, represent hydrogen or C1-C12 alkyl, C3-C12 alkenyl or C3-C12 alkynyl, each optionally substituted by one or more hydroxy groups, C1-C4 alkoxy, C1-C4 alkylthio or phenyl, provided that R ¹ , R ² , R ³ and R ⁴ are sterically compatible. In addition, any two of R ¹ , R ² , R ³ and R ⁴ together can represent an aliphatic difunctional fraction containing one to twelve carbon atoms and up to two oxygen or sulfur atoms. Salts can be prepared by treatment with a metal hydroxide, such as sodium hydroxide, with an amine, such as ammonia, trimethylamine, diethanolamine, 2-methylthiopropylamine, bisalylamine, 2-butoxyethylamine, morpholine, cyclododecylamine, or benzylamine or with a benzylamine hydroxide tetraalkylammonium, such as tetramethyl hydroxide
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15/69 lamonium or choline hydroxide.
Exemplary esters include those derived from C1-C12 alkyl, C3-C12 alkenyl, C3-C12 alkynyl or alkyl alcohols substituted with C7-C10 aryl, such as methyl alcohol, isopropyl alcohol, 1-butanol, 2-ethylexanol, butoxyethanol, methoxypropanol, allyl alcohol, propargyl alcohol, cyclohexanol or benzyl alcohols not substituted or substituted. Benzyl alcohols can be substituted with 1 - 3 substituents independently selected from halogen, C1-C4 alkyl or C1-C4 alkoxy. Esters can be prepared by coupling acids with alcohol using any number of suitable activating agents, such as those used for peptide couplings, such as dicyclohexylcarbodiimide (DCC) or carbonyl diimidazole (CDI); by reacting the acids with alkylating agents, such as alkyl halides or alkyl sulfonates in the presence of a base, such as triethylamine or lithium carbonate; by reacting the corresponding acid chloride of an acid with an appropriate alcohol; by reacting the corresponding acid with an appropriate alcohol in the presence of an acid catalyst or by transesterification.
COMPOSITIONS AND METHODS [0054] Herbicidal compositions are presented here comprising a herbicidally effective amount of (a) a compound of Formula (I)
h ₃ c '° <0 or its agriculturally acceptable salt or ester, and (b) dimethoxy-pyrimidine or its agriculturally acceptable salt or ester.
Vege control methods are also presented here
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16/69 undesirable tact comprising contact with vegetation or its location, that is, the area adjacent to vegetation, or application to soil or water to prevent the emergence or growth of vegetation, with a herbicidally effective amount of the compound of Formula (I) or its agriculturally acceptable salt or ester and (b) a dimethoxy-pyrimidine. In certain embodiments, the methods employ the compositions described herein.
[0055] Furthermore, in some embodiments, the combination of compound (I) or its agriculturally acceptable salt or ester and dimethoxypyrimidine, or its agriculturally acceptable salt or ester exhibits synergy, for example, the herbicidal active ingredients are more effective in combination with than when applied individually. Synergy was defined as "an interaction of two or more factors, so that the effect, when combined, is greater than the expected effect based on the response to each factor applied separately". Senseman, S., ed. Herbicide Handbook. 9th ed. Lawrence: Weed Science Society of America, 2007. In certain embodiments, the compositions exhibit synergy as determined by Colby's equation. Colby, SR 1967. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 15: 20-22.
[0056] In certain embodiments of the compositions and methods described herein, the compound of Formula (I), that is, carboxylic acid is used. In certain embodiments, a carboxylate salt of the compound of Formula (I) is used. In certain embodiments, an aralkyl or alkyl ester is used. In certain embodiments, a benzyl ester, substituted benzyl or C1-4 alkyl, for example, butyl ester, is used. In certain embodiments, the benzyl ester is used.
[0057] In certain embodiments, dimethoxy-pyrimidine is bispiribacsodium, pyribenzoxim, pyriftalid, piriminobac-methyl or pyrimisulfan or its agriculturally acceptable derivative.
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17/69 [0058] In some embodiments, the compound of Formula (I) or its salt or ester and bispiribac sodium, pyribenzoxim, pyriftalid, pyriminobacmethyl and pyrimisulfan or its agriculturally acceptable salt or ester are formulated into a composition, mixed in a tank, applied simultaneously or applied sequentially.
[0059] Herbicidal activity is exhibited by the compounds when they are applied directly to the plant or to the location of the plant at any stage of growth. The observed effect depends on the plant species to be controlled, the growth stage of the plant, the parameters of application of dilution and size of the sprayed drop, the particle size of the solid components, the environmental conditions at the time of use, the specific compound employed, the specific adjuvants and vehicles used, the type of soil and others, as well as the amount of chemical substance applied. These and other factors can be adjusted to promote non-selective or selective herbicidal action. In some embodiments, the compositions described here are applied as a post-emergence application, pre-emergence application or application in water to flooded rice fields or bodies of water (for example, ponds, lakes and streams), vegetation relatively immature undesirable to achieve maximum weed control.
[0060] In some embodiments, the compositions and methods presented here are used to control weeds in crops, including, but not limited to, rice sown directly, sown in water and transplanted, cereals, wheat, barley, oats, rye, sorghum , corn, sugar cane, sunflower, rapeseed, canola, beet, soy, cotton, pineapple, pastures, lawns, pasture, fallow, grass, tree and vineyard orchards, aquatic, plantation crops, vegetables, vegetation control (IVM) and rights of way (ROW).
[0061] In certain modalities, the compositions and methods here
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18/69 presented are used to control weeds in rice. In certain modalities, rice is rice that is sown directly, sown in water or transplanted.
[0062] The compositions and methods described herein can be used to control undesirable vegetation crops tolerant to glyphosate, tolerant to 5-enolpyruvylshikimato-3-phosphate (EPSP) synthase, tolerant to glufosinate, tolerant to glutamine synthase inhibitor, tolerant to dicamba, tolerant to phenoxy auxin, tolerant to pyridyloxy auxin, tolerant to auxin, tolerant to auxin transport inhibitor, tolerant to aryloxyphenoxypropionate, tolerant to cyclohexanedione, tolerant to phenylpyrazoline, tolerant to acetyl CoA carboxylase inhibitor (ACCase), tolerant to imidazone , sulfonylurea tolerant, tolerant to pyrimidinylthiobenzoate, tolerant to triazolopyrimidine, tolerant to sulfonylaminocarbonyltriazolinone, tolerant to acetolactate synthase (ALS) inhibitor or acetohydroxy acid synthase (AHAS), tolerant to 4-hydroxide inhibitor (4-hydroxyphenyl) phytoene desaturase inhibitor, tolerant to inhibition or carotenoid biosynthesis, tolerant to protoporphyrinogen oxidase (PPO) inhibitor, tolerant to cellulose biosynthesis inhibitor, tolerant to mitosis inhibitor, tolerant to microtubule inhibitor, tolerant to very long chain fatty acid inhibitor, tolerant to inhibitor fatty acid and lipid biosynthesis, tolerant to photosystem I inhibitor, tolerant to photosystem II inhibitor, tolerant to triazine and tolerant to bromoxynil (such as, but not limited to, soy, cotton, canola / rapeseed, rice, cereals, corn , sorghum, sunflower, beet, sugar cane, grass, and others), for example, together with glyphosate, EPSP synthase inhibitors, glufosinate, glutamine synthase inhibitors, dicamba, phenoxy auxins, pyridyloxy auxins, synthetic auxins, auxin transport inhibitors, aryloxyphenoxypropionates, cyclohexanediones, phenylpyrazolines, ACCase inhibitors, imidazoline
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19/69 nas, sulfonylureas, pyrimidinylthiobenzoates, triazolopyrimidines, sulfonylaminocarbonyltriazolinones, ALS or AHAS inhibitors, HPPD inhibitors, phytene desaturase inhibitors, carotenoid biosynthesis inhibitors, PPO inhibitors, cellulose inhibitors, cellulose inhibitors, biosynthesis inhibitors microtubules, very long chain fatty acid inhibitors, fatty acid and lipid biosynthesis inhibitors, photosystem I inhibitors, photosystem II inhibitors, triazines, and bromoxynil. The compositions and methods can be used to control undesirable vegetation in crops that have multiple or stacked traits that provide tolerance to multiple chemicals and / or inhibitors of multiple modes of action. In some embodiments, the compound of Formula (I) or its salt or ester and complementary herbicide or its salt or ester are used in combination with herbicides that are selective for the crop being treated and that complement the spectrum of weeds controlled by these compounds at the application rate employed. In some embodiments, the compositions described herein and other complementary herbicides are applied at the same time, as a combination formulation, as a tank mixture, or sequentially.
[0063] Compositions and methods can be used to control undesirable vegetation in crops that have tolerance to agronomic stress (including, but not limited to, drought, cold, heat, salt, water, nutrients, fertility, pH), tolerance to pests (including, but not limited to, insects, fungi and pathogens) and traits of crop improvement (including, but not limited to, yield; protein, carbohydrate or oil content; protein, carbohydrate or oil composition; plant stature and plant architecture).
[0064] The compositions and methods presented here are used to control undesirable vegetation. Undesirable vegetation in
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20/69 includes, but is not limited to, undesirable vegetation that occurs in rice, cereals, wheat, barley, oats, rye, fields and pastures, fallow, row crops (for example, maize, sugar cane, sunflower , rapeseed, canola, beet, soy, cotton), grass, tree orchards and vineyards, plantation crops, vegetables, ornamental, aquatic species or non-harvest environments (eg rights of way, industrial vegetation control).
[0065] In some modalities, the methods presented here are used to control undesirable vegetation in rice. In certain modalities, the undesirable vegetation is Brachiaria platyphylla (Groseb.) Nash or Urochloa platyphylla (Nash) R.D. Webster (taquarinha, BRAPP), Digitaria sanguinalis (L.) Scop. (mattress grass, DIGSA), Echinochloa species (ECHSS), Echinochloa crus-galli (L.) P. Beauv. (capybara grass, ECHCG), Echinochloa crus-pavonis (Kunth) Schult. (rice grass, ECHCV), Echinochloa colonum (L.) LINK (capimarroz, ECHCO), Echinochloa oryzoides (Ard.) Fritsch (rice-corn, ECHOR), Echinochloa oryzicola (Vasinger) Vasinger (rice-corn , ECHPH), Echinochloa phyllopogon (Stapf) Koso-Pol. (rice grass, ECHPH), Echinochloa polystachya (Kunth) Hitchc. (jaime grass, ECHPO), Ischaemum rugosum Salisb. (male grass, ISCRU), Leptochloa chinensis (L.) Nees (Chinese grass, LEFCH), Leptochloa fascicularis (Lam.) Gray (mimoso grass, LEFFA), Leptochloa panicoides (Presl.) Hitchc. (Amazon grass, LEFPA), Oryza species (red and harmful rice, ORYSS), Panicum dichotomiflorum (L.) Michx. (swamp grass, PANDI), Paspalum dilatatum Poir. (sweet grass, PASDI), Rottboellia cochinchinensis (Lour.) W.D. Clayton (hairy grass, ROOEX), Cyperus species (CYPSS), Cyperus difformis L. (juniper, CYPDI), Cyperus dubius Rottb. (MAPDU), Cyperus esculentus L. (yellow sedge, CYPES), Cyperus would L. (sedge, CYPIR), Cyperus rotundus L. (sedge, CYPRO), Cyperus serotinus
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21/69
Rottb./C.B.Clarke (three corners, CYPSE), Eleocharis species (ELOSS), Fimbristylis miliacea (L.) Vahl (cuminho, FIMMI), Schoenoplectus species (SCPSS), Schoenoplectus juncoides Roxb. (rice junk, SCPJU), Bolboschoenus maritimus (L.) Palla or, Schoenoplectus maritimus L. Lye (sea jonquil, SCPMA), Schoenoplectus mucronatus L. (rice jonquil, SCPMU), species of Aeschynomene, (angiquinho, AESSS), Alternanthera philoxeroides (Mart.) Griseb. (alligator grass, ALRPH), Alisma plantago-aquatica L. (water hyacinth, ALSPA), Amaranthus species (bredos and amarantos, AMASS), Ammannia coccinea Rottb. (red stem, AMMCO), Commelina benghalensis L. (comelina, COMBE), Eclipta alba (L.) Hassk. (false daisy from America, ECLAL), Heteranthera limosa (SW.) Willd./Vahl (duck salad, HETLI), Heteranthera reniformis R. & P. (dogress, HETRE), Ipomoea species (morning glory, IPOSS), Ipomoea hederacea (L.) Jacq. (liana, IPOHE), Lindernia dubia (L.) Pennell (dubious lindernia, LIDDU), Ludwigia species (LUDSS), Ludwigia linifolia Poir. (Maltese cross, LUDLI), Ludwigia octovalvis (Jacq.) Raven (Maltese cross, LUDOC), Monochoria korsakowii Regel & Maack (monocory, MOOKA), Monochoria vaginalis (Burm. F.) C. Presl ex Kuhth, (monocory, MOOVA), Murdannia nudiflora (L.) Brenan (pigeon pea, MUDNU), Polygonum pensylvanicum L., (silkworm, POLPY), Polygonum persicaria L. (persicaria, POLPE), Polygonum hydropiperoides Michx. (POLHP, silkworm), Rotala indica (Willd.) Koehne (rotala, ROTIN), Sagittaria species, (sagittarius, SAGSS), Sesbania exaltata (Raf.) Cory / Rydb. Ex Hill (Sesbania, SEBEX), or Sphenoclea zeylanica Gaertn. (goose-grass, SPDZE).
[0066] In some modalities, the methods presented here are used to control undesirable vegetation in cereals. In certain embodiments, the undesirable vegetation is Alopecurus myosuroides Huds. (foxtail-grass, ALOMY), Apera spica-venti (L.) Be
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22/69 auv. (apera, APESV), Avena fatua L. (wild oats, AVEFA), Bromus tectorum L. (bromine, BROTE), Lolium multiflorum Lam. (ryegrass, LOLMU), Phalaris minor Retz. (talaceiro, PHAMI), Poa annua L. (hen-foot, POANN), Setaria pumila (Poir.) Roemer & J.A. Schultes (yellow corn, SETLU), Setaria viridis (L.) Beauv. (green corn, SETVI), Amaranthus retroflexus L. (giant caruru, AMARE), Brassica species (BRSSS), Chenopodium album L. (white ansarina, CHEAL), Cirsium arvense (L.) Scop. (thistle, CIRAR), Galium aparine L. (catch, GALAP), Kochia scoparia (L.) Schrad. (kochia, KCHSC), Lamium purpureum L. (purple lamina, LAMPU), Matricaria recutita L. (wild chamomile, MATCH), Matricaria matricarioides (Less.) Porter (matricaria, MATMT), Papaver rhoeas L. (common poppy, PAPRH ), Polygonum convolvulus L. (deer vine, POLCO), Salsola tragus L. (Russian thistle, SASKR), Sinapis species (SINSS), Sinapis arvensis L. (wild mustard, SINAR), Stellaria media (L. ) Vill. (morugem, STEME), Veronica persica Poir. (veronica-of-persia, VERPE), Viola arvensis Murr. (field violet, VIOAR), or Viola tricolor L. (wild violet, VIOTR).
[0067] In some modalities, the methods presented here are used to control undesirable vegetation in fields and pastures, fallows, IVM and ROW. In certain embodiments, the undesirable vegetation is Ambrosia artemisiifolia L. (carpenter, AMBEL), Cassia obtusifolia (senna, CASOB), Centaurea maculosa auct. non Lam. (centaurea maculosa, CENMA), Cirsium arvense (L.) Scop. (thistle, CIRAR), Convolvulus arvensis L. (morning glory, CONAR), Daucus carota L. (wild carrot, DAUCA), Euphorbia esula L. (euphorbia, EPHES), Lactuca serriola L./Torn. (prickly lettuce, LACSE), Plantago lanceolata L. (sheep tongue, PLALA), Rumex obtusifolius L. (cow tongue, RUMOB), Sida spinosa L. (malvinha, SIDSP), Sinapis arvensis L. (wild mustard , SINAR), Sonchus arvensis L. (perennial thistle, SONAR), species
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23/69 species of Solidago (golden rod, SOOSS), Taraxacum officinale G.H. Weber ex Wiggers (dandelion, TAROF), Trifolium repens L. (common clover, TRFRE), or Urtica dioica L. (dioic nettle, URTDI).
[0068] In some modalities, the methods presented here are used to control undesirable vegetation found in row crops, tree and vineyard crops and perennial crops. In certain embodiments, the undesirable vegetation is Alopecurus myosuroides Huds. (foxtail grass, ALOMY), Avena fatua L. (wild oats, AVEFA), Brachiaria decumbens Stapf. or Urochloa decumbens (Stapf) R.D. Webster (Surinam grass, BRADC), Brachiaria brizantha (Hochst. ex A. Rich.) Stapf. or Urochloa brizantha (Hochst. ex A. Rich.) RD (bearded grass, BRABR), Brachiaria platyphylla (Groseb.) Nash or Urochloa platyphylla (Nash) RD Webster (taquarinha, BRAPP), Brachiaria plantaginea (Link) Hitchc . or Urochloa plantaginea (Link) R.D. Webster (papuã, BRAPL), Cenchrus echinatus L. (grass-carrapixo, CENEC), Digitaria horizontalis Willd. (mattress grass, DIGHO), Digitaria insularis (L.) Mez ex Ekman (bitter grass, TRCIN), Digitaria sanguinalis (L.) Scop. (mattress grass, DIGSA), Echinochloa crus-galli (L.) P. Beauv. (capybara grass, ECHCG), Echinochloa colonum (L.) Link (rice grass, ECHCO), Eleusine indica (L.) Gaertn. (goose grass, ELEIN), Lolium multiflorum Lam. (ryegrass, LOLMU), Panicum dichotomiflorum Michx. (dobanhado grass, PANDI), Panicum miliaceum L. (millet, PANMI), Setaria faberi Herrm. (fox-tailed grass, SETFA), Setaria viridis (L.) Beauv. (green corn, SETVI), Sorghum halepense (L.) Pers. (massambará grass, SORHA), Sorghum bicolor (L.) Moench ssp. Arundinaceum (sergoforrageiro, SORVU), Cyperus esculentus L. (yellow sedge, CYPES), Cyperus rotundus L. (sedge, CYPRO), Abutilon theophrasti Medik. (jute-da-china, ABUTH), Amaranthus species (bredos and amarantos, AMASS), Ambrosia artemisiifolia L. (carpenter, AMBEL), Ambrosia
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24/69 psilostachya DC. (tap, AMBPS), Ambrosia trifida L. (giant tap, AMBTR), Anoda cristata (L.) Schlecht. (mallow, ANVCR), Asclepias syriaca L. (asclepias, ASCSY), Bidens pilosa L. (black pick, BIDPI), Borreria species (BOISS), Borreria alata (Aubl.) DC. or Spermacoce alata Aubl. (borreria, BOILF), Spermacose latifolia (herbaceous, BOILF), Chenopodium album L. (white ansarina, CHEAL), Cirsium arvense (L.) Scop. (thistle, CIRAR), Commelina benghalensis L. (comelina, COMBE), Datura stramonium L. (datura, DATST), Daucus carota L. (wild carrot, DAUCA), Euphorbia heterophylla L. (peanuts, EPHHL), Euphorbia hirta L. or Chamaesyce hirta (L.) Millsp. (swallowtail, EPHHI), Euphorbia dentata Michx. (milk-toothed, EPHDE), Erigeron bonariensis L. or Conyza bonariensis (L.) Cronq. (buva, ERIBO), Erigeron canadensis L. (voadeira, ERICA), Conyza sumatrensis (Retz.) EH Walker (avavinha-ivory, ERIFL), Helianthus annuus L. (common sunflower, HELAN), Jacquemontia tamnifolia (L.) Griseb . (small flower ipomea, IAQTA), Ipomoea hederacea (L.) Jacq. (cipozinho, IPOHE), Ipomoea lacunosa L. (white morning glory, IPOLA), Lactuca serriola L./Torn. (prickly lettuce, LACSE), Portulaca oleracea L. (purslane, POROL), Richardia species (poaiado-cerrado, RCHSS), Sida species (sida, SIDSS), Sida spinosa L. (malvinha, SIDSP), Sinapis arvensis L (wild mustard, SINAR), Solanum ptychanthum Dunal (belladonna, SOLPT), Tridax procumbens L. (bullgrass, TRQPR), or Xanthium strumarium L. (bardanamenor, XANST). In some modalities, the methods presented here are used to control unwanted grass vegetation. In certain embodiments, the undesirable vegetation is Bellis perennis L. (daisy, BELPE), Cyperus esculentus L. (yellow tiririca, CYPES), Cyperus species (CYPSS), Digitaria sanguinalis (L.) Scop. (capimcolchão, DIGSA), Diodia virginiana L. (hot grass, DIQVI), Euphorbia species (euphorbia, EPHSS), Glechoma hederacea L. (ivy,
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25/69
GLEHE), Hydrocotyle umbellata L. (acariçoba, HYDUM), Kyllinga species (kyllinga, KYLSS), Lamium amplexicaule L. (white nettle, LAMAM), Murdannia nudiflora (L.) Brenan (pigeon weed, MUDNU), species of Oxalis (sorrel, OXASS), Plantago major L. (plantain, PLAMA), Plantago lanceolata L. (carrijó, PLALA), Phyllanthus urinaria L. (stone breaker, PYLTE), Rumex obtusifolius L. (tongue- devaca, RUMOB), Stachys floridana Shuttlew. (Japan-cut, STAFL), Stellaria media (L.) Vill. (morugem, STEME), Taraxacum officinale G.H. Weber ex Wiggers (dandelion, TAROF), Trifolium repens L. (common clover, TRFRE), or Viola species (wild violet, VIOSS).
[0069] In some embodiments, the compositions and methods presented here are used to control undesirable vegetation consisting of grassy, broad-leaved weeds and weeds. In certain embodiments, the compositions and methods presented here are used to control undesirable vegetation including Cyperus, Digitaria, Echinochloa, Fimbristylis, Ipomoea, Leptochloa and Schoenoplectus.
[0070] In some embodiments, the combination of compound (I) or its agriculturally acceptable ester or salt and bispiribac-sodium, pyribenzoxim, pyriftalid, pyriminobac-methyl and pyrimisulfan or its agriculturally acceptable salt or ester is used to control Cyperus rotundus, Digitaria sanguinalis, Echinochloa crus-galli, Echinochloa colona, Fimbristylis miliacea, Ipomoea hederacea, Leptochloa chinensis and Schoenoplectus maritimus or Bolboschoenus maritimus.
[0071] Formula I compounds or their agriculturally acceptable salt or ester can be used to control herbicide-resistant or tolerant weeds. Methods that employ the combination of a Formula I compound or its agriculturally acceptable salt or ester and the compositions described herein may also
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26/69 be used to control herbicide resistant or tolerant weeds. Exemplary resistant or tolerant weeds include, but are not limited to, biotypes resistant or tolerant to acetolactate synthase (ALS) or acetohydroxy acid synthase (AHAS) inhibitors (for example, imidazolinones, sulfonylureas, dimethoxypyrimidines, triazolopyrimidines, and sulfonylsilaminylsilaminylsilaminylsilaminylsilaminylsilaminylsilaminylsilaminylamine). of photosystem II (for example, phenylcarbamates, pyridazinones, triazines, triazinones, uracils, amides, ureas, benzothiadiazinones, nitriles, phenylpyridazines), acetyl CoA carboxylase (ACCase) inhibitors (for example, aryloxyphenoxypropionates, phenoxyphenyls, cyclohexanines, cyclohexanines, cyclohexanines, cyclohexanines, cyclohexanines, cyclohexanines, cyclamines, (eg benzoic acids, phenoxycarboxylic acids, pyridinecarboxylic acids, quinolinecarboxylic acids), auxin transport inhibitors (eg phthalates, semicarbazones), photosystem I inhibitors (eg bipyridyls), 5-enolpyruvilshikimato-3- phosphate (EPSP) synthase (for example, g lifosate), glutamine synthetase inhibitors (eg, glufosinate, bialafos), microtubule assembly inhibitors (eg, benzamides, benzoic acids, dinitroanilines, phosphoramidates, pyridines), mitosis inhibitors (eg carbamates), acid inhibitors very long chain fatty acids (VLCFA) (eg acetamides, chloroacetamides, oxyacetamides, tetrazolinones), fatty acid and lipid synthesis inhibitors (eg phosphorodithioates, thiocarbamates, benzofurans, chlorocarbon acids), protoporphyrogen oxidase (PPO) inhibitors (for example, diphenyl ethers, N-phenylphthalimides, oxadiazoles, oxazolidinediones, phenylpyrazoles, pyrimidindiones, thiadiazoles, triazolinones), carotenoid biosynthesis inhibitors (eg clomazone, amitrol, aclonifen), inhibitors (eg phytase) , amides, anilidex, furanones, phenoxybutan-amides, pyridiazinones, pyridines), 4-hydroxyphenylpyruvate dioxigen inhibitors ase (HPPD) (for example, calistemones,
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27/69 isoxazoles, pyrazoles, tricetones), cellulose biosynthesis inhibitors (eg nitriles, benzamides, quinclorac, triazolocarboxamides), herbicides with multiple modes of action, such as quinclorac, and unclassified herbicides, such as arylaminopropionic acids, difenzoquat, endotal and organoarsenic. Exemplary resistant or tolerant weeds include, but are not limited to, biotypes with resistance or tolerance to multiple herbicides, biotypes with resistance or tolerance to multiple chemical classes, biotypes with resistance or tolerance to multiple modes of herbicidal action and biotypes with multiple mechanisms of resistance or tolerance (eg target site resistance or metabolic resistance).
[0072] In some embodiments, an agriculturally acceptable ester or salt of compound (I) is used. In certain embodiments, an agriculturally acceptable ester is used. In certain embodiments, the ester is a C1-4 alkyl ester. In certain embodiments, the ester is an n-butyl ester. In certain embodiments, the ester is a benzyl ester. In certain embodiments, a compound (I) is used which is a carboxylic acid.
[0073] In some embodiments, an agriculturally acceptable ester or salt of bispyribac-sodium, pyribenzoxim, pyriftalid, pyriminobacmethyl and pyrimisulfan is used in the methods or compositions described herein. In certain embodiments, bispiribac sodium salt is used.
[0074] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with bispiribac-sodium or carboxylic acid or its ester or other salt of bispiribac. With respect to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to bispiribac-sodium or carboxylic acid or its ester or other salt of bispiribac is within the range of about 1:75 at about 43: 1. In certain embodiments, the weight ratio of the compound of Formula (I)
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28/69 or its salt or ester for bispiribac-sodium or its salt or ester is within the range of about 1: 9 to about 10: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to bispiribac-sodium or carboxylic acid or its ester or other salt of bispiribac is within the range of about 1:10 to about 7: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to bispiribac-sodium or carboxylic acid or its ester or other salt of bispiribac is within the range of about 1: 5 to about 3, 5: 1. In certain embodiments, the compositions presented herein comprise the compound of Formula (I) or its benzyl or butyl ester and bispyribac-sodium. In one embodiment, the composition comprises the compound of Formula (I) and bispiribac-sodium, wherein the weight ratio of the compound of Formula (I) to bispiribac-sodium is from about 1: 3 to about 3.5: 1 . In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and bispyribacsodium, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to bispyribac-sodium is from about 1: 5 to about 2.5: 1. In one embodiment, the composition comprises the n-butyl ester of the compound of Formula (I) and bispiribac-sodium, wherein the weight ratio of the n-butyl ester of the compound of Formula (I) to bispiribac-sodium is about 1: 1.1 to about 1.75: 1. With respect to methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the emergence or growth of vegetation with a composition described herein. In some embodiments, the composition is applied at an application rate of about 9 grams of active ingredient per hectare (gai / ha) to about 450 gai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 12 grams of active ingredient per hectare (gai / ha) to about 110 gai / ha based
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29/69 in the total amount of active ingredients in the composition. In some embodiments, the methods comprise contacting undesirable vegetation or its location or application to soil or water to prevent the emergence or growth of vegetation with a compound of Formula (I) or its salt or ester and bispiribac-sodium or carboxylic acid or its ester or other bispiribac salt, for example, sequentially or simultaneously. In some embodiments, bispiribac-sodium or carboxylic acid or its ester or other salt of bispiribac is applied at a rate of about 7 gai / ha to about 150 gai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 2 g of acid equivalent (ae) / ha to about 300 gae / ha. In some embodiments, bispiribac-sodium or carboxylic acid or its ester or other bispiribac salt is applied at a rate of about 3 gai / ha to about 80 gai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 4 g of acid equivalent per hectare (gae / ha) to about 150 gae / ha. In some embodiments, bispiribac-sodium or carboxylic acid or its ester or other salt of bispiribac is applied at a rate of about 7 gai / ha to about 40 gai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 8.75 g of acid equivalent per hectare (gae / ha) to about 70 gae / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl or n-butyl ester and bispyribacsodium. In one embodiment, the methods use the compound of Formula (I) and bispiribac-sodium, in which the compound of Formula (I) is applied at a rate of about 8.75 g of acid equivalent per hectare (gae / ha ) at about 42.4 gae / ha, and bispiribac-sodium is applied at a rate of about 10 gai / ha to about 40 gai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and bispiribac-sodium, in which the benzyl ester of the compound of Formula (I) is applied at a rate of about 4.38 g of acid equivalent per
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30/69 hectare (gae / ha) at about 70 gae / ha, and bispiribac-sodium is applied at a rate of about 7 gai / ha to about 40 gai / ha. In one embodiment, the methods use the n-butyl ester of the compound of Formula (I) and bispiribac-sodium, in which the n-butyl ester of the compound of Formula (I) is applied at a rate of about 35 g of equivalent of acid per hectare (gae / ha) to about 70 gae / ha, and bispiribac-sodium is applied at a rate of about 40 gai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with bispiribac-sodium or carboxylic acid or its ester or other bispiribac salt are used to control LEFCH, ECHCG, ECHOR, CYPRO or SCPMA.
[0075] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with pyribenzoxim or its salt or ester. With respect to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyribenzoxim or its salt or ester is within the range of about 1:45 to about 10: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyribenzoxim or its salt or ester is within the range of 1:12 to about 2: 1. In certain embodiments, the compositions comprise the compound of Formula (I) or its benzyl or n-butyl ester and pyribenzoxy. With respect to methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the emergence or growth of vegetation with a composition described herein. In some embodiments, the composition is applied at an application rate of about 17 grams of active ingredient per hectare (gai / ha) to about 360 gai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 20 grams of active ingredient per
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31/69 hectare (gai / ha) to about 200 gai / ha based on the total amount of active ingredients in the composition. In some embodiments, the methods comprise contact of undesirable vegetation or its location or application to soil or water to prevent the emergence or growth of vegetation with a compound of Formula (I) or its salt or ester and pyribenzoxim, for example, sequential or simultaneously. In some embodiments, pyribenzoxim or its salt or ester is applied at a rate of about 15 gai / ha to about 60 gai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 2 g of acid equivalent (ae) / ha to about 300 gae / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl or n-butyl ester and pyribenzoxy.
[0076] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with pyribenzoxim or its salt or ester. With respect to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyribenzoxy or its salt or ester is within the range of about 1:45 to about 10: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyribenzoxy or its salt or ester is within the range of 1: 9 to about 1: 4. In certain embodiments, the compositions comprise the compound of Formula (I) or its benzyl or n-butyl ester and pyribenzoxy. With respect to methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the emergence or growth of vegetation with a composition described herein. In some embodiments, the composition is applied at an application rate of about 17 grams of active ingredient per hectare (gai / ha) to about 360 gai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied to
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32/69 an application rate of about 20 grams of active ingredient per hectare (gai / ha) to about 200 gai / ha based on the total amount of active ingredients in the composition. In additional special modalities, the composition is applied at an application rate of about 78 grams of active ingredient per hectare (gai / ha) to about 90 gai / ha based on the total amount of active ingredients in the composition. In some embodiments, the methods comprise contact of undesirable vegetation or its location or application to soil or water to prevent the emergence or growth of vegetation with a compound of Formula (I) or its salt or ester and pyribenzoxim, for example, sequential or simultaneously. In some embodiments, pyribenzoxim or its salt or ester is applied at a rate of about 15 gai / ha to about 60 gai / ha and the compound of Formula (I) or its salt or ester is applied at a rate of about from 2 g of acid equivalent (ae) / ha to about 300 gae / ha. In certain embodiments, methods using the compound of Formula (I) or its benzyl or butyl ester and pyribenzoxim and are used to control ECHCG.
[0077] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with pyriftalid or carboxylic acid or its carboxylate salt or other ester. With respect to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyriftalid or carboxylic acid or its carboxylate salt or other ester is within the range of about 1: 150 to about 3: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyriftalid or carboxylic acid or its carboxylate salt or other ester is within the range of about 1:20 to about 1: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyriftalid or carboxylic acid or its carboxylate salt or other ester is within the range of about 1:36 to about 2: 1. In
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In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyriftalid or carboxylic acid or its carboxylate salt or other ester is within the range of about 1:18 to about 1: 1 , 4. In certain embodiments, the compositions presented herein comprise the compound of Formula (I) or its benzyl or butyl ester and pyriftalid. In one embodiment, the composition comprises the compound of Formula (I) and pyriftalid, wherein the weight ratio of the compound of Formula (I) to pyriftalid is about 1:18 to about 1: 1.4. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and pyriftalid, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to pyriftalid is from about 1:18 to about 1: 2.6. With respect to methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the emergence or growth of vegetation with a composition described herein. In some embodiments, the composition is applied at an application rate of about 102 grams of active ingredient per hectare (gai / ha) to about 600 gai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 49 grams of active ingredient per hectare (gai / ha) to about 125 gai / ha based on the total amount of active ingredients in the composition. In some embodiments, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the emergence or growth of vegetation with a compound of Formula (I) or its salt or ester and pyriftalid or carboxylic acid or its carboxylate salt or other ester, for example, sequentially or simultaneously. In some embodiments, pyriftalid or carboxylic acid or its carboxylate salt or other ester is applied at a rate of about 45 gai / ha to about 300 gai / ha, and the compound of Formula (I) or its salt or ester is applied to
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34/69 a rate of about 2 g of acid equivalent (ae) / ha to about 300 gae / ha. In some embodiments, pyriftalid or carboxylic acid or its carboxylate salt or other ester is applied at a rate of about 20 gai / ha to about 180 gai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 2 g of acid equivalent per hectare (gae / ha) to about 70 gae / ha. In some embodiments, pyriftalid or carboxylic acid or its carboxylate salt or other ester is applied at a rate of about 45 gai / ha to about 90 gai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 4.38 g of acid equivalent per hectare (gae / ha) to about 35 gae / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl or n-butyl ester and pyriftalid. In one embodiment, the methods use the compound of Formula (I) and pyriftalid, in which the compound of Formula (I) is applied at a rate of about 4.38 g of acid equivalent per hectare (gae / ha) at about 35 gae / ha, and pyriftalid is applied at a rate of about 45 gai / ha to about 90 gai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and pyriftalid, in which the benzyl ester of the compound of Formula (I) is applied at a rate of about 4.38 g of acid equivalent per hectare (gae / ha) at about 17.5 gae / ha, and pyriftalid is applied at a rate of about 45 gai / ha to about 90 gai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with pyriftalid or carboxylic acid or its carboxylate salt or other ester are used to control BRAPP, LEFCH, CYPRO, or FIMMI.
[0078] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with pyriminobac-methyl or carboxylic acid or its carboxylate salt or other ester. Regarding the compositions, in some
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35/69 embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyriminobac-methyl or carboxylic acid or its carboxylate salt or other ester is within the range of about 1:45 to about 27: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyriminobac-methyl or carboxylic acid or its carboxylate salt or other ester is within the range of about 1:20 to about 3: 1 . In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyriminobac-methyl or carboxylic acid or its carboxylate salt or other ester is within the range of about 1:20 to about 4: 1 . In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyriminobac-methyl or carboxylic acid or its carboxylate salt or other ester is within the range of about 1: 9 to about 1.6 :1. In certain embodiments, the compositions presented herein comprise the compound of Formula (I) or its benzyl or n-butyl ester and pyriminobac-methyl. In one embodiment, the composition comprises the compound of Formula (I) and pyriminobac-methyl, wherein the weight ratio of the compound of Formula (I) to pyriminobac-methyl is from about 1: 5 to about 1.6: 1. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and pyriminobac-methyl, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to pyriminobac-methyl is about 1: 9 to about 1.6: 1. With respect to methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the emergence or growth of vegetation with a composition described herein. In some embodiments, the composition is applied at an application rate of about 13 grams of active ingredient per hectare (gai / ha) to about 390 gai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 15 grams of
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36/69 active ingredient per hectare (gai / ha) to about 125 gai / ha based on the total amount of active ingredients in the composition. In some embodiments, the methods comprise contacting undesirable vegetation or its location or application to soil or water to prevent the emergence or growth of vegetation with a compound of Formula (I) or its salt or ester and pyriminobac-methyl or carboxylic acid or its carboxylate salt or other ester, for example, sequentially or simultaneously. In some embodiments, pyriminobac-methyl or carboxylic acid or its carboxylate salt or other ester is applied at a rate of about 11 gai / ha to about 90 gai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 2 gai / ha to about 300 g of acid equivalent (ae) / ha. In some embodiments, pyriminobac-methyl or carboxylic acid or its carboxylate salt or other ester is applied at a rate of about 5 gai / ha to about 180 gai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 2 g of acid equivalent per hectare (gae / ha) to about 140 gae / ha. In some embodiments, pyriminobac-methyl or carboxylic acid or its carboxylate salt or other ester is applied at a rate of about 11.25 gai / ha to about 90 gai / ha and the compound of Formula (I) or its salt or ester is applied at a rate of about 4.38 g of acid equivalent per hectare (gae / ha) to about 70 gae / ha. In certain embodiments, the methods use the compound of Formula (I), or its benzyl or n-butyl ester and pyriminobac-methyl. In one embodiment, the methods use the compound of Formula (I) and pyriminobac-methyl, where the compound of Formula (I) is applied at a rate of about 4.38 g of acid equivalent per hectare (gae / ha ) at about 70 gae / ha, and pyriminobac-methyl is applied at a rate of about 11.25 gai / ha to about 90 gai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and pyriminobac-methyl, in which the benzyl ester of the
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37/69 post of Formula (I) is applied at a rate of about 4.38 g of acid equivalent per hectare (gae / ha) to about 35 gae / ha, and pyriminobac-methyl is applied at a rate of about 11.25 gai / ha to about 90 gai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with pyriminobac-methyl or carboxylic acid or its carboxylate salt or other ester are used to control DIGSA, IPOHE, LEFCH, ECHCO, FIMMI, SCPMA or CYPRO.
[0079] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with pyrimisulfan or its salt or ester. With respect to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyrimisulfan or its salt or ester is within the range of about 1: 100 to about 30: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pyrimisulfan or its salt or ester is within the range of 1:45 to about 10: 1. In certain embodiments, the compositions presented herein comprise the compound of Formula (I) or its benzyl or n-butyl ester and pyrimisulfan. With respect to methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the emergence or growth of vegetation with a composition described herein. In some embodiments, the composition is applied at an application rate of about 12 grams of active ingredient per hectare (gai / ha) to about 500 gai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 15 grams of active ingredient per hectare (gai / ha) to about 300 gai / ha based on the total amount of active ingredients in the composition. In some modalities, the methods comprise the contact of the ve
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38/69 undesirable growth or its location or application to soil or water to prevent the emergence or growth of vegetation with a compound of Formula (I) or its salt or ester and pyrimisulfan or its salt or ester, for example, sequentially or simultaneously . In some embodiments, pyrimisulfan or its salt or ester is applied at a rate of about 10 gai / ha to about 200 gai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 2 gae / ha to about 300 gae / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl or n-butyl ester and pyrimisulfan.
[0080] The components of the mixtures described here can be applied separately or as part of a multi-part herbicide system.
[0081] The mixtures described here can be applied in conjunction with one or more other herbicides to control a wider variety of undesirable vegetation. When used in conjunction with other herbicides, the composition can be formulated with the other herbicide or herbicides, mixed in tank with the other herbicide or herbicides or applied sequentially with the other herbicide or herbicides. Some of the herbicides that can be used in conjunction with the compositions and methods described herein include, but are not limited to: 4-CPA; 4-CPB; 4-CPP; 2,4-D; 2,4-D choline salt, 2,4-D, 2,4-DB esters and amines; 3,4-DA; 3,4-DB; 2,4-DEB; 2,4-DEP; 3.4DP; 2,3,6-TBA; 2,4,5-T; 2,4,5-TB; acetochlor, acifluorfen, aclonifen, acrolein, alachlor, alidochlor, aloxidim, allyl alcohol, alorac, ametridione, amethrine, amibuzine, amicarbazone, amidosulfuron, aminocyclopyrachlor, aminopiralid, amiprofos-methyl, amitron, amitron, amitrol, amitrol, sulphate , atrazine, azafenidin, azimsulfuron, aziprotrin, barban, BCPC, beflubutamid, benazoline, bencarbazone, benfluralin, benfuresate, bensulfuron-methyl, bensulide, bentiocarb,
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39/69 bentazon-sodium, benzadox, benzfendizone, benzipram, benzobicyclon, benzofenap, benzofluor, benzoilprop, benztiazuron, bialafos, bicyclopyrone, bifenox, bilanafos, borax, bromacil, bromobonyl, bromoboxy, butromobromide, bromophenyl, bromophenyl , butenachlor, butidazole, butiuron, butralin, butroxidim, buturon, butylate, cacodylic acid, cafenstrol, calcium chlorate, calcium cyanamide, cambendichlor, carbasulam, carbetamide, carboxazole chlorprocarb, carfentrazone-ethyl, CDEA, chloren, clen, CEPC, clom, CEPC, clom, , clorazifop, chlorazin, clorbromuron, chlororbam, chloreturon, chlorfenac, chlorfenprop, chlorflurazol, chlorflurenol, chloridazon, chlorimuron, chlornitrofen, chloropon, chlorotoluron, chloroxuron, chloroxynil, chlorprofam, cinchloridon, chlorinyl, chloride, chloride , cletodim, cliodinato, clodinafop-propargil, clofop, clomazone, clomeprop, cloprop, cloproxidim, clopyralid, chloransulam-methyl, CMA, south copper suit, CPMF, CPPC, credazine, cresol, cumiluron, cyanatrine, cyanazine, cyclate, cyclopyrimorate, cyclosulfamuron, cycloxidim, cycluron, cyhalofop-butyl, cyperquat, cyprazine, cyprazole, cypromid, daimuron, delimom, dalapon, dalapon, dalapon, dalapon, dalapon desmetrine, di-alate, dicamba, dichlobenyl, dichloralurea, dichlormate, dichlorprop, dichlorprop-P, diclofopmethyl, diclosulam, dietamquat, diethyl, diphenopenten, difenoxuron, difenzoquat, diflufenican, diflufen, dimlufen, dimetifamide, dimlufen, dimen P, dimexane, dimidazon, dinitramine, dinofenate, dinoprop, dinosam, dinoseb, dinoterb, diphenamid, dipropetrin, diquat, disul, dithiopir, diuron, DMPA, DNOC, DSMA, EBEP, eglinazine, endotal, epronaz, EPTC, erbon, espronaz, ercar, espr etalfluralin, etbenzamide, etametsulfuron, etidimuron, etiolate, etobenzamid, etobenzamid, etofumesate, ethoxyfen, ethoxysulfuron, ethinophen, etnipromid, etobenzanid, EXD, fenasulam, fenpropa, fenoxaprop, fenoxaprop, fenoxaprop, fenoxaprop -P-ethyl + isoxadifen-ethyl, phenoxasulfone, fenteracol, fentiaprop, fentrazamide, fenuron, ferrous sulfate, flamprop,
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40/69 flamprop-M, flazasulfuron, florasulam, fluazifop, fluazifop-P-butyl, fluazolate, flucarbazone, flucetosulfuron, flucloraline, flufenacet, flufenican, flufenpir-ethyl, flumetsulam, flumezine, flumicloroxil, flumicloroxil-pentomethane , fluoroglycofen, fluoromidine, fluoronitrophen, fluotiuron, flupoxam, flupropacil, flupropanate, flupirsulfuron, fluridone, flurochloridone, fluroxypyr, fluroxypyridine, flurtamone, flutiacet, fomesafen, glufurin, gluten, phospho-fluoride, gluten -ammonium, glyphosate, halosafen, halauxifen, halauxifen-methyl, halosulfuron-methyl, haloxidine, haloxifop-methyl, haloxifop-P-methyl, hexachloroacetone, hexaflurate, hexazinone, imazametabenz, imazamma, imazamoxan, imazamox, imazapox, imazapiz, imazapox, imazapox, imazamox, imazam, , indaziflam, iodobonil, iodomethane, iodosulfuron, iodosulfuron-ethyl-sodium, iofensulfuron, ioxynil, ipazine, ipfencarbazone, iprimidam, isocarbamid, isocyl, isometil iozine, isonoruron, isopolinate, isopropalin, isoproturon, isouron, isoxaben, isoxaclortol, isoxaflutol, isoxapirifop, carbutilate, cetospiradox, lactofen, lenacil, linuron, esters and amines of MAA, MOP, MCAP, MCMA, MCPA, MCAP, MCPA, MCPA, MCAP, MCPA, MCAP, MCPA, MCAP, MCPA, P, medinoterb, mefenacet, mefluidide, mesoprazine, mesosulfuron, mesotrione, metam, metamifop, metamitron, metazachlor, metazosulfuron, metflurazon, metabenztiazuron, metallopralin, metazol, metiobencarb, methiozetho, methiozetho, methiozetho, methiozetho, methiozetone, methiozetho, methiozetho, methiozone methyldimron, metobenzuron, metobromuron, metolachlor, metosulam, methoxyuron, metribuzin, metsulfuron, metsulfuron-methyl, molinate, monalide, monisouron, monochloroacetic acid, monolinuron, monuron, morfamquat, MSMA, naproanilamide, nanopropyl, nanopropyl , nitrofen, nitrofluorfen, norflurazon, noruron, OCH, orbencarb, ortho-dichlorobenzene, ortosulfamuron, orizaline, oxadiargyl, oxadiazon, oxapirazon, ox asulfuron, oxaziclomefone, oxyfluorfen, paraflufen-ethyl, parafluron, paraquat, pebulate, pelargonic acid, pendime
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41/69 talina, penoxsulam, pentachlorophenol, pentanochlor, pentoxazone, perfluidone, petoxamid, fenisofam, fenmedifam, fenmedifam-ethyl, fenobenzuron, phenylmercury acetate, picloram, picolinafen, pinoxaden, potassium, arsenite, potassium, arsenite , pretilachlor, primisulfuron-methyl, prociazine, prodiamine, profluazole, profluralin, profoxidim, proglinazine, proexadione-calcium, prometon, promethine, pronamide, propachlor, propanyl, propaquizafop, propazine, propam, propisochlor, propoxycarbonate, propoxycarbonate, propoxycarbonate , prosulfuron, proxan, prinaclor, pidanon, piraclonil, piraflufen-ethyl, pirasulfotol, pyrazogyl, pyrazolinate, pirazosulfuron-ethyl, pyrazoxifen, pyributicarb, piriclor, pyridafol, pyridate, pyrimisulfan, pyroxoxacyramine, pyroxoxacloramine, pyroxoxacloramine, pyroxoxacloramine, pyroxoxacloramine, pyroxoxacloramine, pyroxoxamine , quinonamid, quizalofop, quizalofop-P-ethyl, rhodetanil, rimsulfuron, saflufenacil, S-metolachlor, sebutilazine, secbumeton, setoxidim, siduron, simazine, simeton, symmetrine, SMA, sodium arsenite, sodium azide, sodium chlorate, sulcotrione, sulfalate, sulfentrazone, sulfometuron, sulfosate, sulfosulfuron, sulfuric acid, sulglicapine, swep, SIN-523, TCA, tebut , tebutiuron, tefuriltrione, tembotrione, tepraloxidim, terbacil, terbucarb, terbuclor, terbumeton, terbutilazine, terbutrin, tetrafluron, tenilchlor, thiazafluron, tiazopir, tidiazimine, tidiazuron, tidiazuron, tenciazuron, tencbazone, tencbazone , tralcoxidim, triafamone, tri-alate, triasulfuron, triaziflam, tribenuron, tribenuron-methyl, tricamba, triclopyr choline salt, triclopyr esters and salts, tridiphane, trietazine, trifloxysulfuron, trifluralin, trifluralin, trifluralin, trifluralin, trifluralin, trifluralin, trifluralin, trifluralin , tripropindan, tritac tritosulfuron, vernolate, xylachlor and its salts, esters, optically active isomers and mixtures.
[0082] The compositions and methods described herein can also be used in conjunction with glyphosate, 5enolpyruvylshikimato-3-phosphate (EPSP) synthetase inhibitors, glufosinate, inhibitors
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42/69 of glutamine synthetase, dicamba, phenoxy auxins, pyridyloxy auxins, synthetic auxins, auxin transport inhibitors, aryloxyphenoxypropionates, cyclohexanediones, phenylpyrazolines, acetyl CoA carboxylase inhibitors (ACCase), imidazolinines, sulfonylsilinylsulphonylsilines, sulfonylsilinylsulphines acetolactate synthase (ALS) or acetohydroxy acid synthase (AHAS), 4-hydroxyphenylpyruvate dioxigenase (HPPD) inhibitors, phytene desaturase inhibitors, carotenoid biosynthesis inhibitors, protoporphyrinogen oxidase inhibitors (PPO), cellulose inhibitors , mitosis inhibitors, microtubule inhibitors, very long chain fatty acid inhibitors, fatty acid and lipid biosynthesis inhibitors, photosystem I inhibitors, photosystem II inhibitors, triazines, and crops tolerant to bromoxynil or glyphosate, tolerant to inhibitor of EPSP synthetase, toleran glufosinate, tolerant to glutamine synthase inhibitor, tolerant to dicamba, tolerant to phenoxy auxin, tolerant to pyridyloxy auxin, tolerant to auxin, tolerant to auxin transport inhibitor, tolerant to aryloxyphenoxypropionate, tolerant to cyclohexanodione, tolerant to phenylpirazoline ACCase, tolerant to imidazolinone, tolerant to sulfonylurea, tolerant to pyrimidinylthiobenzoate, tolerant to triazolopyrimidine, tolerant to sulfonylaminocarbonyltriazolinone, tolerant to ALS- or AHAS, tolerant to HPPD, tolerant to inhibitors of phytenoid inhibitors, desaturase, to PPO, tolerant to cellulose biosynthesis inhibitor, tolerant to mitosis inhibitor, tolerant to microtubule inhibitor, tolerant to very long chain fatty acid inhibitor, tolerant to fatty acid and lipid biosynthesis inhibitor, tolerant to photosystem inhibitor I, tolerant to phot inhibitor ossystem II, triazine-tolerant, bromoxynil-tolerant, and having multiple or stacked traits that confirm tolerance to multiple chemicals and / or multiple modes
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43/69 of action through single and / or multiple resistance mechanisms. In some embodiments, the compound of Formula (I) or its salt or ester and the complementary herbicide or its salt or ester are used in combination with herbicides that are selective for the crop being treated and that complement the spectrum of controlled weeds these compounds at the application rate used. In some embodiments, the compositions described herein and other complementary herbicides are applied at the same time, as a combination formulation, as a tank mix or as a sequential application.
[0083] In some embodiments, the compositions described here are used in combination with one or more protectors against herbicides, such as AD-67 (MON 4660), benoxacor, bentiocarb, brassinolide, cloquintocet (mexil), ciometrinil, daimuron, diclormid, diciclonon , dimepiperate, disulfoton, fenclorazol-ethyl, fenclorim, flurazol, fluxofenim, furilazol, hairpin proteins, isoxadifen-ethyl, jiecaowan, jiecaoxi, mefenpir-diethyl, mefenate, naphthalic anhydride (NA), amine oxide and amine; N-phenyl-sulfonylbenzoic acid, to increase its selectivity. In some modalities, the protectors are used in rice, cereal or corn environments. In some embodiments, the protector is cloquintocet or its ester or salt. In certain embodiments, cloquintocet is used to antagonize harmful effects of the compositions on rice and cereals. In some embodiments, the protector is cloquintocet (mexil).
[0084] In some embodiments, the compositions described herein are used in combination with one or more plant growth regulators, such as 2,3,5-triiodiodobenzoic acid, IAA, IBA, naphthaleneacetamide, α-naphthalenoacetic acids, benzyladenine, 4hydroxyphenethyl alcohol, kinetin, zeatin, endotal, etefon, pentachlorophenol, thidiazuron, tribufos, maleic aviglycine hydrazide, gibberellins, acid
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44/69 gibberellic acid, abscisic acid, ancimidol, phosamine, glyphosine, isopyrimole, jasmonic acid, maleic hydrazide, mepiquat, 2,3,5-triiodobenzoic acid, morphactins, dichlorflurenol, flurprimidol, mefluidide, paclobiclacisol, brassyl, hexanazole, tinclobutrazol, brassyl -ethyl, cycloheximide, ethylene, metasulfocarb, proexadione, triapentenol and trinexapac.
[0085] In some modalities, plant growth regulators are used in one or more crops or environments, such as rice, cereal crops, corn, broadleaf crops, rapeseed / canola, grass, pineapple, sugar cane , sunflower, pastures, lawns, pastures, fallow, orchards of trees and vineyards, crops of plantation, vegetables and non-harvest environments (ornamental). In some embodiments, the plant growth regulator is mixed with the compound of Formula (I), or mixed with the compound of Formula (I) and a dimethoxy-pyrimidine to preferably cause an advantageous effect on plants.
[0086] In some embodiments, the compositions presented here also comprise at least one agriculturally acceptable adjuvant or vehicle. Suitable adjuvants or vehicles should not be phytotoxic for valuable crops, particularly at the concentrations used in the application of compositions for selective weed control in the presence of crops and should not react chemically with herbicidal components or other ingredients in the composition. These mixtures can be designed for application directly to weeds or their location or they can be concentrated or formulations that are normally diluted with additional vehicles and adjuvants before application. They can be solid, such as powders, granules, water-dispersible granules or wetting powders, or liquids, such as emulsifiable concentrates, solutions, emulsions or suspensions. They can also be
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45/69 as a premix or mixed in a tank.
[0087] Suitable agricultural adjuvants and vehicles include, but are not limited to, harvest oil concentrate; nonylphenol ethoxylate; benzylcocoalkylimethyl quaternary ammonium salt; mixture of petroleum hydrocarbons, alkyl esters, organic acids and anionic surfactants; C9-C11 alkyl polyglycoside; phosphate alcohol ethoxylate; natural primary alcohol ethoxylate (C12-C16); di-sec-butylphenol, EO-PO block copolymer; polysiloxane-methyl cap; nonylphenol ethoxylate + urea ammonium nitrate; emulsified methylated seed oil; tridecyl alcohol (synthetic) ethoxylate (8EO); tallow amine ethoxylate (15 EO); PEG (400) dioleate-99.
[0088] Liquid vehicles that can be used include water and organic solvents. Organic solvents include, but are not limited to, petroleum fractions or hydrocarbons, such as mineral oil, aromatic solvents, paraffinic oils and others; vegetable oils such as soybean oil, rapeseed oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cottonseed oil, flaxseed oil, palm oil, palm oil, peanuts, safflower oil, sesame oil, tung oil and others; esters of the above vegetable oils; esters of monoalcohols or dihydric, trihydric or lower polyalcohols (containing 4 - 6 hydroxides), such as 2-ethyl hexyl stearate, n-butyl oleate, isopropyl myristate, propylene glycol dioleate, di-octyl succinate, di-octyl adipate butyl, dioctyl phthalate and others; esters of mono-, di- and polycarboxylic acids and others. Specific organic solvents include, but are not limited to, toluene, xylene, petroleum naphtha, harvest oil, acetone, methyl ethyl ketone, cyclohexanone, trichlorethylene, perchlorethylene, ethyl acetate, amyl acetate, butyl acetate, propylene glycol ether monomethyl and diethylene glycol monomethyl ether, methyl alcohol, ethyl alcohol, isopropyl alcohol, amyl alcohol, ethylene glycol, propylene glycol, glycerin, N
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46/69 methyl-2-pyrrolidinone, N, N-dimethyl alkylamides, dimethyl sulfoxide, liquid fertilizers and others. In certain embodiments, water is the vehicle for diluting concentrates.
[0089] Suitable solid vehicles include, but are not limited to, talc, pyrophyllite clay, silica, atapulgite clay, kaolin clay, kieselguhr, chalk, diatomaceous earth, lime, calcium carbonate, bentonite clay, Fuller earth, seed husks cotton, wheat flour, soy flour, pumice, wood flour, nutshell flour, lignin, cellulose and others.
[0090] In some embodiments, the compositions described herein also comprise one or more surfactants. In some embodiments, these surfactants are used in both solid and liquid compositions and, in certain embodiments, those designed to be diluted with a vehicle before application. Surfactants can be of anionic, cationic or non-ionic character and can be used as emulsifying agents, wetting agents, suspending agents or for other purposes. Surfactants that can also be used in the present formulations are described, among others, in “McCutcheon's Detergents and Emulsifiers Annual,” MC Publishing Corp., Ridgewood, New Jersey, 1998 and in “Encyclopedia of Surfactants,” Vol. I-III, Chemical Publishing Co., New York, 1980-81. Surfactants include, but are not limited to, alkyl sulfate salts, such as diethanolammonium lauryl sulfate; alkylarylsulfonate salts, such as calcium dodecylbenzenesulfonate; alkylphenol-alkylene oxide addition products, such as nonylphenol-Cw ethoxylate; alcohol-alkylene oxide addition products, such as C16 ethoxylate tridecyl alcohol; soaps, such as sodium stearate; alkylnaphthalene sulfonate salts, such as sodium dibutylnaphthalenesulfonate; dialkyl esters of sulfosuccinate salts, such as sodium di (2-ethylexyl) sulfosuccinate; sorbitol esters, such as sorbitol oleate; amines
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Quaternary 47/69, such as lauryl trimethylammonium chloride; polyethylene glycolic esters of fatty acids, such as polyethylene glycol stearate; block copolymers of ethylene oxide and propylene oxide; salts of mono- and dialkyl phosphate esters; vegetable or seed oils, such as soybean oil, rapeseed / canola oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cottonseed oil, linseed oil, oil palm oil, peanut oil, safflower oil, sesame oil, tung oil and others; and esters of the above vegetable oils and, in certain embodiments, methyl esters.
[0091] In some embodiments, these materials, such as vegetable or seed oils and their esters, can be used interchangeably as an agricultural adjuvant, as a liquid vehicle or as a surfactant.
[0092] Other exemplary additives for use in the composition presented herein include, but are not limited to, compatibilizing agents, antifoaming agents, sequestering agents, neutralizing agents and buffers, corrosion inhibitors, dyes, odorants, spreading agents, penetration aids , tackifiers, dispersing agents, thickening agents, freezing point depressants, antimicrobial agents and others. The compositions can also contain other compatible components, for example, other herbicides, plant growth regulators, fungicides, insecticides and others and can be formulated with liquid fertilizers or solid particulate fertilizer vehicles, such as ammonium nitrate, urea and others.
[0093] In some embodiments, the concentration of active ingredients in the compositions described here is about 0.0005 to 98 weight percent. In some embodiments, the concentration is about 0.0006 to 90 weight percent. In compositions designed to be used as concentrates, the active ingredients, in certain
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48/69 modalities are present in a concentration of about 0.1 to 98 weight percent and, in certain modalities, from about 0.5 to 90 weight percent. These compositions are, in certain embodiments, diluted with an inert carrier, such as water, before application. The diluted compositions normally applied to weeds or the weed site contain, in certain embodiments, from about 0.0006 to 3.0 percent by weight of active ingredient and, in certain embodiments, contain from about 0.01 to 1.0 weight percent.
[0094] The present compositions can be applied to weeds or their location with the use of conventional terrestrial or aerial powderers, sprays and granule applicators, by addition to irrigation water or rice paddies and by other conventional means known to those skilled in the art. in the technique.
[0095] The modalities described and the following examples are for illustrative purposes and are not intended to limit the scope of the claims. Other modifications, uses or combinations with respect to the compositions described herein will be clear to those skilled in the art, without departing from the spirit and scope of the claimed matter.
Examples [0096] The results in Examples I and II are greenhouse test results.
Example I. Evaluation of Herbicidal Mixtures of Foliar Application in Post-emergence For Weed Control in Direct Sowing Rice [0097] Seeds or nuts of the desired test plant species were planted in a soil matrix prepared by mixing a soil of marna or sandy marna (eg 28.6 percent sludge, 18.8 percent clay and 52.6 percent sand, with a pH of about 5.8 and an organic matter content of about 1.8 percent) and limestone in a ratio of 80 to 20. The soil matrix is
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49/69 was contained in plastic vases with a volume of 0.95 liters (1 quarter) and a surface area of 83.6 square centimeters (cm ² ). When required to ensure good germination and healthy plants, a fungicidal treatment and / or other chemical or physical treatment was applied. The plants were grown for 8 - 22 days in a greenhouse with a photoperiod of approximately 14 h which was maintained at about 29 ° C during the day and 26 ° C at night. Nutrients (Peters Excel® 15-5-15 5-Ca 2-Mg and iron chelate) were applied to the irrigation solution when necessary, and water was added on a regular basis. Supplementary lighting was provided with suspended 1000 Watt metal halide lamps when needed. The plants were used for testing when they reached the first to the fourth stage of true leaf.
[0098] The treatments consisted of the amino acid or esters of 4 amino-3- chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxy-phenyl) pyridine-2-carboxylic acid (Compound A), each formulated as a SC (concentrated in suspension), and in various herbicidal components alone or in combination. Compound A forms were applied based on the acid equivalent.
[0099] The forms of compound A (compound of Formula I) tested include:
Acid Compound
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Compound A Benzyl ester [00100] Other herbicidal components were applied based on an active ingredient and included the dimethoxy-pyrimidine acetolactate synthase (ALS) bispyribac-sodium inhibitor herbicides formulated as Regiment® 80WP, pyribenzoxim (technical quality material), piriminobac-methyl formulated as Hie-Clean® 1.2% GR dissolved in water, and pyriftalid (technical quality material).
[00101] Treatment requirements were calculated based on the rates being tested, the concentration of active ingredient or acid equivalent in the formulation, and an application volume of 12 mL at a rate of 187 L / ha.
[00102] For treatments that comprised formulated compounds, the measured amounts of compounds were placed individually in 25 ml glass bottles and diluted in a volume of 1.25% (v / v) crop oil concentrate Agri-Dex® to obtain 12X stock solutions. If a test compound did not readily dissolve, the mixture was heated and / or sonicated. The application solutions were prepared by adding an appropriate amount of each stock solution (for example, 1 ml) and diluted to the appropriate final concentrations with the addition of 10 ml of an aqueous mixture of harvest oil concentrate at 1.25 % (v / v), so that the final spray solutions contained 1.25 +/- 0.005% (v / v) harvest oil concentrate.
[00103] For treatments that comprised technical compounds,
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51/69 the weighed quantities can be placed individually in 25 ml glass vials and dissolved in a 97: 3 v / v volume of acetone / DMSO to obtain 12X stock solutions. If a test compound did not readily dissolve, the mixture could be heated and / or sonicated. Application solutions can be prepared by adding an appropriate amount of each stock solution (for example, 1 mL) and diluted to the appropriate final concentrations with the addition of 10 mL of an aqueous mixture of harvest oil concentrate to 1, 5% (v / v), so that the final spray solutions contained 1.25% (v / v) harvest oil concentrate. When technical materials were used, the concentrated stock solutions could be added to the spray solutions so that the final concentrations of acetone and DMSO in the application solutions were 16.2% and 0.5%, respectively.
[00104] For treatments that comprised formulated and technical compounds, the heavy quantities of the technical materials were placed individually in 25 mL glass vials and dissolved in a 97: 3 v / v volume of acetone / DMSO to obtain stock solutions at 12X, and the measured quantities of the formulated compounds were placed individually in 25 ml glass bottles and diluted in a volume of 1.5% (v / v) harvest oil concentrate or water to obtain stock solutions at 12X. If a test compound did not readily dissolve, the mixture was heated and / or sonicated. The application solutions were prepared by adding an appropriate amount of each stock solution (for example, 1 mL) and diluted to the appropriate final concentrations with the addition of an appropriate amount of an aqueous mixture of harvest oil concentrate to 1, 5% (v / v), so that the final spray solutions contained 1.25% (v / v) harvest oil concentrate. When required, additional 97: 3 v / v water and / or acetone / DMSO was
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52/69 added to individual application solutions, so that the final concentrations of acetone and DMSO of the application solutions being compared were 8.1% and 0.25%, respectively.
[00105] All stock solutions and application solutions were visually inspected for compatibility of the compound prior to application. The spray solutions were applied to the plant material with a suspended Mandel sprayer equipped with 8002E nozzles calibrated to distribute 187 L / ha over an application area of 0.503 m ² at a spray height of 46 to 50 cm (18 to 20 inches) ) above the average plant crown height. Control plants were sprayed in the same way with solvent only.
[00106] The treated plants and the control plants were placed in a greenhouse as described above and watered by sub-irrigation to prevent loss of test compounds. After approximately 3 weeks, the condition of the test plants compared to that of untreated plants was determined visually and rated on a scale of 0 to 100 percent, where 0 corresponds to no injury or growth inhibition, and 100 corresponds to complete death.
[00107] Colby's equation was used to determine the expected herbicidal effects of the mixtures (Colby, S.R. 1967. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 15: 20-22.).
[00108] The following equation was used to calculate the expected activity of mixtures containing two active ingredients, A and B:
Expected = A + B - (A x B / 100)
A = observed effectiveness of active ingredient A at the same concentration as that used in the mixture.
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B = observed effectiveness of active ingredient B at the same concentration as that used in the mixture.
The compounds tested, the application rates used, the plant species tested and the results are given in Tables 1 - 6.
Table 1. Synergistic Activity of Herbicidal Compositions of Compound Benzyl Ester and Bispiribac-Sodium of Foliar Application on Weed Control in a Rice Harvest System.
Benzyl ester compound Bispiribac-Sodium Visual Weed Control (%) - 20 DAA LEFCH gae / ha gai / ha Note Esp 8.75 0 10 - 17.5 0 20 - 0 7 0 - 0 14 0 - 8.75 7 25 10 17.5 7 40 20 8.75 14 25 10 17.5 14 60 20
Table 2. Synergistic Activity of Herbicidal Compositions of Compound Benzyl Ester and Pyribenzoxim of Foliar Application on the Control of Weeds in a Rice Harvest System.
Benzyl ester compound Piribenzoxim Visual Weed Control(%) - 20 DAA ECHCG gae / ha gai / ha Note Esp 8 0 75 -
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Benzyl ester compound Piribenzoxim Visual Weed Control(%) - 20 DAA ECHCG 16 0 85 - 0 70 85 - 8 70 99 96 16 70 99 98
Table 3. Synergistic Activity of Herbicidal Compositions of Acid Compound and Pyriminobac-Methyl Foliar Application on Weed Control in a Rice Harvest System.
Acid Compound Piriminobacmetil Visual Weed Control (%) -24 DAA DIGSA IPOHE gae / ha gai / ha Note Esp Note Esp 4.38 0 20 - 10 - 8.75 0 25 - 10 - 17.5 0 25 - 30 - 0 11.25 0 - 10 - 0 22.5 0 - 10 - 4.38 11.25 30 20 15 19 8.75 11.25 45 25 30 19 17.5 11.25 60 25 60 37 4.38 22.5 15 20 20 19 8.75 22.5 40 25 20 19 17.5 22.5 40 25 45 37
Compound AAcid Piriminobacmetil Visual Weed Control(%) - 24 DAA IPOHE
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Compound AAcid Piriminobacmetil Visual Weed Control(%) - 24 DAA gae / ha gai / ha Note Esp 17.5 0 25 - 35 0 48 - 0 90 20 - 17.5 90 43 40 35 90 70 58
Table 4. Synergistic Activity of Herbicidal Compositions of Compound Benzyl Ester and Pyriminobac-methyl of Foliar Application on the Control of Weeds in a Harvest System
Rice.
Compound ABenzyl ester Piriminobacmetil Visual Weed Control(%) - 24 DAA LEFCH IPOHE gae / ha gai / ha Note Esp Note Esp 4.38 0 0 - 10 - 8.75 0 0 - 15 - 17.5 0 10 - 30 - 0 11.25 0 - 10 - 0 22.5 0 - 10 - 4.38 11.25 20 0 25 19 8.75 11.25 15 0 40 24 17.5 11.25 40 10 30 37 4.38 22.5 15 0 40 19 8.75 22.5 15 0 20 24 17.5 22.5 40 10 40 37
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Compound ABenzyl ester Piriminobacmetil Visual Control of Damaged Herbs lines (%) - 21 DAA IPOHEgae / ha gai / ha Note Esp 17.5 0 43 - 0 90 20 - 17.5 90 65 54 Table 5. Synergistic Activity of Her Compositions composites
to Acid and Piriftalid of Foliar Application on Weed Control in a Rice Harvest System.
Acid Compound Piriftalid Visual Weed Control (%) - 22DAA BRAPP gae / ha gai / ha Note Esp 4.38 0 45 - 0 45 0 - 0 90 0 - 4.38 45 65 45 4.38 90 65 45
Table 6. Synergistic Activity of Herbicidal Compositions of Compound Benzyl Ester and Pyriftalid Foliar Application on the Control of Weeds in a Rice Harvest System.
Benzyl ester compound Piriftalid Visual Weed Control(%) - 22 DAA LEFCH gae / ha gai / ha Note Esp 17.5 0 25 - 0 45 0 - 0 90 0 - 17.5 45 40 25
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Benzyl ester compound Piriftalid Visual Weed Control(%) - 22 DAA LEFCH gae / ha gai / ha Note Esp 17.5 90 35 25
BRAPP Brachiaria platyphylla (Griseb.) Nash taquarinha, broad leaf
DIGSA Digitaria sanguinalis (L.) Scop.
ECHCG Echinochloa crusgalli (L.) Beauv.
IPOHE Ipomoea hederacea Jacq.
mattress grass, large
Cipozinho capybara grass
LEFCH Leptochloa chinensis (L.) Nees Chinese grass gae / ha = grams of acid equivalent per hectare gai / ha = grams of active ingredient per hectare
Obs = observed value
Esp = Expected value as calculated by the Colby equation
DAA = days after application
Example II. Evaluation of Herbicidal Mixtures Applied in Water Regarding Weed Control in Transplanted Rice Rice [00109] Seeds of weeds or nuts of the desired test plant species were planted in wet soil (mud) prepared by mixing a non-mineral soil sterilized and in pieces (50.5 percent sludge, 25.5 percent clay and 24 percent sand, with a pH of about 7.6 and an organic matter content of about 2.9 percent) and water at a volumetric ratio of 1: 1. The prepared sludge was distributed in 365 ml aliquots in 0.47 liter (16 oz (oz) unperforated plastic pots with a surface area of 86.59 square centimeters (cm ² ) leaving an upper space of 3 centimeters (cm) in each pot. The sludge was allowed to dry overnight before planting or transplanting. The rice seeds were planted in a Sun Gro MetroMix 306 planting mixture, which typically has a pH of 6.0 to 6.8 and an organic matter content of
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58/69 about 30 percent, in plastic seedling trays. Seedlings in the second or third stage of leaf growth were transplanted into 860 mL of mud contained in 0.94 L (32-oz) unperforated plastic pots with a surface area of 86.59 cm ² 4 days before application of the herbicide. The rice field was created by filling the upper space of the pots with 2.5 to 3 cm of water. When required to ensure good germination and healthy plants, a fungicide treatment and / or other chemical or physical treatment was applied. The plants were grown for 4 - 22 days in a greenhouse with an approximate photoperiod of 14 h which was maintained at about 29 ° C during the day and 26 ° C at night. Nutrients were added as Osmocote® (19: 6: 12, N: P: K + minor nutrients) to 2 g per 0.47 L (16-oz) pot and 4 g per 0.94 L pot (32- oz). Water was added on a regular basis to maintain the rice paddies, and supplementary lighting was provided with suspended 1000 Watt metal halide lamps as needed. The plants were used for testing when they reached the first to the fourth stage of true leaf.
[00110] The treatments consisted of 4 amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxy-phenyl) pyridine-2-carboxylic acid (esters A) each formulated as a SC and several herbicide components alone or in combination. Compound A forms were applied based on the acid equivalent.
[00111] The forms of compound A (compound of Formula I) tested include:
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Acid Compound
N-Butyl Ester Compound
Compound A Benzyl ester [00112] Other herbicidal components were applied based on an active ingredient and included the dimethoxy-pyrimidine acetolactate synthase (ALS) bispiribac-sodium inhibitor herbicides formulated as Regiment® 80 WP, pyriminobac-methyl formulated as HieClean® , and pyriftalid (technical quality material).
[00113] The treatment requirements for each herbicide compound or component were calculated based on the rates being tested, the concentration of active ingredient or equivalent
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60/69 acid in the formulation, an application volume of 2 ml per component per pot and an application area of 86.59 cm ² per pot.
[00114] For formulated compounds, a measured quantity was placed in an individual glass bottle of 100 or 200 mL and was dissolved in a volume of 1.25% (v / v) Agri-Dex® harvest oil concentrate for if application solutions are obtained. If the test compound did not readily dissolve, the mixture was heated and / or sonicated.
[00115] For compounds of technical quality, a measured quantity was placed in an individual glass bottle of 100 or 200 mL and was dissolved in a volume of acetone to obtain concentrated stock solutions. If the test compound did not readily dissolve, the mixture was heated and / or sonicated. The concentrated stock solutions were diluted with an equivalent volume of an aqueous mixture containing 2.5% (v / v) harvest oil concentrate, so that the final application solutions contained 1.25 harvest oil concentrate % (v / v).
[00116] The applications were made by injection with a pipette of appropriate quantities of the solutions for application, individually and sequentially, in the aqueous layer of the rice field. The control plants were treated in the same way only with the solvent. Applications were made so that all treated plant material received the same concentrations of acetone and harvest oil concentrate.
[00117] The treated plants and the control plants were placed in a greenhouse as described above, and water was added as needed to keep the paddy field flooded. After approximately 3 weeks, the condition of the test plants compared to that of untreated plants was determined visually and rated on a scale of 0 to 100 percent, where 0 corresponds to
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61/69 no injury or growth inhibition, and 100 corresponds to complete death.
[00118] Colby's equation was used to determine the expected herbicidal effects of the mixtures (Colby, S.R. 1967. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 15: 20-22.).
[00119] The following equation was used to calculate the expected mixing activity containing two active ingredients, A and B:
Expected = A + B - (A x B / 100)
A = observed effectiveness of active ingredient A at the same concentration as that used in the mixture.
B = observed effectiveness of active ingredient B at the same concentration as that used in the mixture.
[00120] Some of the tested compounds, the application rates used, the plant species tested and the results are given in Tables 7 - 13.
Table 7. Synergistic Activity of Water Applications of Herbicidal Compositions of Acid Compound and Bispiribac-Sodium on Weed Control in a Rice Harvest System.
Acid Compound Bispiribac sodium Visual Herb ControlWeeds (%) - 20 DAA ECHCG gae / ha gai / ha Note Esp 8.75 0 0 - 17.5 0 35 - 35 0 55 - 0 10 20 - 0 20 35 - 8.75 10 45 20
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Acid Compound Bispiribac sodium Visual Herb ControlWeeds (%) - 20 DAA ECHCG gae / ha gai / ha Note Esp 17.5 10 30 48 35 10 80 64 8.75 20 60 35 17.5 20 100 58 35 20 99 71
Acid Compound Bispiribac sodium Visual Weed Control (%) - 20DAA ECHOR LEFCH SCPMA gae / ha gai / ha Note Esp Note Esp Note Esp 42.4 0 18 - 15 - 0 - 0 40 30 - 28 - 38 - 42.4 40 62 42 58 38 90 38
Table 8. Synergistic Activity of Water Applications
Herbicidal Compositions of Benzyl Ester Compound and Bispiribacsodium on Weed Control in a Rice Harvest System.
Benzyl ester compound Bispiribac sodium Visual Weed Control (%) - 20 DAA CYPRO gae / ha gai / ha Note Esp 4.38 0 50 - 0 10 0 - 0 20 0 - 4.38 10 70 50 4.38 20 95 50
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Benzyl ester compound Bispiribac sodium Visual Weed Control (%) - 20 DAA SCPMA gae / ha gai / ha Note Esp 35 0 0 - 70 0 0 - 0 40 38 - 35 40 100 38 70 40 95 38
Table 9. Synergistic Activity of Water Applications of Herbicidal Compositions of Compound of N-Butyl Ester and Bispiribac-Sodium on Weed Control in a Rice Harvest System.
N-Butyl Ester Compound Bispiribac sodium Visual Weed Control (%) - 20 DAA ECHOR gae / ha gai / ha Note Esp 35 0 35 - 70 0 40 - 0 40 30 - 35 40 68 55 70 40 100 58
Ester Compound n-Butyl Bispiribac sodium Visual Herb ControlWeeds (%) - 20 DAA SCPMA gae / ha gai / ha Note Esp 70 0 0 - 0 40 38 -
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CompoundButyl Ester n- Bispiribac sodium Visual Herb ControlWeeds (%) - 20 DAA SCPMAgae / hagai / ha Note Esp 7040 75 38 Table 10. Assets Synergistic Effect of Water Applications
Herbicidal Compositions of Acid Compound and Pyriminobac-methyl on Weed Control in a Rice Harvest System.
Compound AAcid Piriminobacmetil Visual Weed Control (%) - 21 DAA ECHCO gae / ha gai / ha Note Esp 8.75 0 0 - 17.5 0 20 - 0 22.5 40 - 8.75 22.5 100 40 17.5 22.5 95 52
Compound AAcid Piriminobacmetil Visual Weed Control (%) - 21 DAA LEFCH gae / ha gai / ha Note Esp 8.75 0 0 - 17.5 0 0 - 0 45 80 - 8.75 45 100 80 17.5 45 100 80
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Acid Compound Piriminobacmetil Visual Weed Control (%) -21 DAA FIMMI SCPMA gae / ha gai / ha Note Esp Note Esp 8.75 0 50 - 0 - 17.5 0 85 - 0 - 35 0 85 - 0 - 0 22.5 0 - 0 - 0 45 0 - 0 - 8.75 22.5 80 50 0 0 17.5 22.5 100 85 30 0 35 22.5 100 85 100 0 8.75 45 85 50 95 0 17.5 45 100 85 30 0 35 45 100 85 95 0
Compound AAcid Piriminobac-methyl Visual Weed Control (%) - 20 DAA SCPMA gae / ha gai / ha Note Esp 35 0 0 - 70 0 0 - 0 90 43 - 35 90 53 43 70 90 85 43
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Table 11. Synergistic Activity of Water Applications of Herbicidal Compositions of Compound Benzyl Ester and Pyriminobac-methyl on Weed Control in a Rice Harvest System.
Compound ABenzyl ester Piriminobac-methyl Visual Weed Control (%) - 21 DAA CYPRO gae / ha gai / ha Note Esp 4.38 0 0 - 8.75 0 20 - 17.5 0 10 - 0 22.5 0 - 4.38 22.5 30 0 8.75 22.5 40 20 17.5 22.5 90 10
Benzyl ester compound Piriminobacmetil Visual Weed Control (%) - 21 DAA SCPMA gae / ha gai / ha Note Esp 4.38 0 0 - 8.75 0 0 - 0 22.5 0 - 0 45 0 - 4.38 22.5 60 0 8.75 22.5 20 0 4.38 45 20 0 8.75 45 20 0
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Benzyl ester compound Piriminobacmetil Visual Weed Control (%) - 20 DAA SCPMA gae / ha gai / ha Note Esp 35 0 0 - 0 90 43 - 35 90 65 43
Table 12. Synergistic Activity of Water Applications of Herbicidal Compositions of Acid Compound and Pyriftalid on Weed Control in a Rice Harvest System.
Acid Compound Piriftalid Visual Weed Control (%) - 21DAA CYPRO gae / ha gai / ha Note Esp 8.75 0 30 - 17.5 0 40 - 35 0 70 - 0 45 0 - 0 90 0 - 8.75 45 85 30 17.5 45 20 40 35 45 80 70 8.75 90 50 30 17.5 90 50 40 35 90 85 70
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Table 13. Synergistic Activity of Water Applications of Herbicidal Compositions of Compound Benzyl Ester and Pyriftalid on Weed Control in a Rice Harvest System.
Compound ABenzyl ester Piriftalid Visual Weed Control (%) - 21DAA CYPRO gae / ha gai / ha Note Esp 4.38 0 30 - 8.75 0 60 - 0 45 0 - 0 90 0 - 4.38 45 40 30 8.75 45 85 60 4.38 90 50 30 8.75 90 100 60
Compound AEsterbenzyl Piriftalid Visual Weed Control(%) - 21 DAA FIMMI gae / ha gai / ha Note Esp 4.38 0 20 - 0 45 50 - 0 90 30 - 4.38 45 100 60 4.38 90 90 44 CYPRO Cyperus rotundus L. iriricão
ECHCG Echinochloa crusgalli (L.) Beauv. capybara grass
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ECHCO Echinochloa colona (L.) Link grass-rice FIMMI Fimbristylis miliacea (L.) Vahl cuminho LEFCH Leptochloa chinensis (L.) Nees Chinese grass SCPMA Bolboschoenus maritimus (L.) Palla. sea jonquil
gae / ha = grams of acid equivalent per hectare gai / ha = grams of active ingredient per hectare Obs = observed value
Esp = Expected value as calculated by the Colby equation
DAA = days after application

权利要求:
Claims (9)
[1]
1. Synergistic herbicidal composition, characterized by the fact that it comprises a herbicidally effective amount of:
(a) a compound of Formula (I):

h ₃ c '° ⁽ⁱ⁾ or butyl or benzyl ester of the compound of Formula (I), and (b) a dimethoxy-pyrimidine, a salt, carboxylic acid, or an agriculturally acceptable carboxylate salt thereof, selected from the group consisting of bispiribac-sodium, pyribenzoxim, pyriminobac-methyl or pyriftalid;
where (a) is a compound of Formula (I), or butyl or benzyl ester thereof, and (b) is bispiribac-sodium, the weight ratio of (a) to (b) is 1: 0, 3 to 1: 4.6;
when (a) is a compound of Formula (I), or benzyl ester thereof, and (b) is pyribenzoxim, the weight ratio from (a) to (b) is from 1: 9 to 1: 4;
when (a) is a compound of Formula (I), or benzyl ester thereof, and (b) is pyriminobac-methyl, the weight ratio of (a) to (b) is 1.6: 1 to 1: 9;
when (a) is a compound of Formula (I), or benzyl ester thereof, and (b) pyriftalid, the weight ratio of (a) to (b) is 0.75: 1 to 1:21.
[2]
2. Composition, according to claim 1, characterized by the fact that it also comprises an adjuvant or vehicle
Petition 870190063052, of 07/05/2019, p. 6/13
2/3 agriculturally acceptable.
[3]
3. Composition, according to claim 1 or 2, characterized by the fact that it also comprises a herbicide protector.
[4]
4. Method for controlling undesirable vegetation, characterized by the fact that it comprises the step of:
contacting a plant, vegetation or its location with soil or water, the soil or water allowing vegetation to grow, with a herbicidally effective amount of a composition, as defined in any of claims 1 to 3.
[5]
5. Method, according to claim 4, characterized by the fact that the vegetation is controlled in rice directly sown, sown in the water and transplanted, cereals, wheat, barley, oats, rye, sorghum, corn, sugar cane , sunflower, rapeseed, canola, beet, soy, cotton, pineapple, pastures, lawns, pastures, fallow, grass, orchards of trees and vineyards, aquatic, industrial vegetation control (IVM) or rights of way (ROW).
[6]
6. Method according to claim 4 or 5, characterized by the fact that (a) and (b) are applied pre-emergence to the weed or harvest.
[7]
7. Method according to any of claims 4 to 6, characterized by the fact that the vegetation is controlled in crops tolerant to glyphosate, 5-enolpyruvylshikimato-3 phosphate (EPSP) synthase, glufosinate, glutamine synthase inhibitor, dicamba, phenoxy auxin, pyridyloxy auxin, synthetic auxin, auxin transport inhibitor, aryloxyphenoxypropionate, cyclohexanedione, phenylpyrazoline, acetyl CoA carboxylase inhibitor (ACCase), imidazolinone, sulfonylurea, pyrimidinyl thiobenzylate, sulfonylamine, triazolone, triazolone acetohydroxy acid synthase (AHAS), 4-hydroxyphenyl-pyruvate dio-
Petition 870190063052, of 07/05/2019, p. 7/13
3/3 xigenase (HPPD), phytene desaturase inhibitor, carotenoid biosynthesis inhibitor, protoporphyrinogen oxidase (PPO) inhibitor, cellulose biosynthesis inhibitor, mitosis inhibitor, microtubule inhibitor, very long chain fatty acid inhibitor, inhibitor of fatty acid and lipid biosynthesis, inhibitor of photosystem I, inhibitor of photosystem II, triazine or bromoxynil.
[8]
8. Method according to claim 7, characterized by the fact that the tolerant harvest has multiple or stacked features that confer tolerance to multiple herbicides or multiple modes of action.
[9]
Method according to any one of claims 4 to 8, characterized in that the undesirable vegetation comprises a herbicide resistant or tolerant plant.

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CN104145982A|2014-08-28|2014-11-19|联保作物科技有限公司|Wheat field weeding composition and medicine preparation thereof|

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CN106172410A|2016-07-13|2016-12-07|北京燕化永乐生物科技股份有限公司|There is the Herbicidal combinations of potentiation|

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CN107751207A|2016-08-17|2018-03-06|燕化永乐（乐亭）生物科技有限公司|A kind of Herbicidal combinations|

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CN107751208A|2016-08-19|2018-03-06|燕化永乐（乐亭）生物科技有限公司|A kind of complex weedicide|

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CN107771813A|2016-08-25|2018-03-09|燕化永乐（乐亭）生物科技有限公司|A kind of Herbicidal combinations|

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WO2019040113A1|2017-08-25|2019-02-28|Dow Agrosciences Llc|Safened herbicidal compositions containing halauxifen or 4-amino-3-chloro-6--5-fluoropyridine-2-carboxylic acid and methods of use thereof in centipedegrass|

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CN109362737A|2018-11-13|2019-02-22|佛山市盈辉作物科学有限公司|A kind of Herbicidal combinations of containing chlorine fluorine pyridine ester and KIH 6127|

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CN110800749A|2019-11-05|2020-02-18|安徽众邦生物工程有限公司|Weeding composition containing halauxifen-methyl and pyriftalid|

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CN111202074A|2019-12-27|2020-05-29|安徽众邦生物工程有限公司|Weeding composition containing halauxifen-methyl and bispyribac-sodium|

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CN111919849A|2020-08-29|2020-11-13|青岛恒宁生物科技有限公司|Weeding composition containing halauxifen-methyl and pyribenzoxim and application thereof|

法律状态:
2015-03-03| B03A| Publication of a patent application or of a certificate of addition of invention [chapter 3.1 patent gazette]|

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2016-10-11| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|

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2018-08-14| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]|

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2018-12-11| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]|

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2019-04-09| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]|

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2019-12-10| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|

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2020-02-04| B16A| Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 19/07/2013, OBSERVADAS AS CONDICOES LEGAIS. |

优先权:

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申请号 | 申请日 | 专利标题

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US201261675109P| true| 2012-07-24|2012-07-24|

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US201261675117P| true| 2012-07-24|2012-07-24|

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US13/833,362|US8871680B2|2012-07-24|2013-03-15|Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6- pyridine-2-carboxylic acid or a derivative thereof and a di-methoxy-pyrimidine and derivatives thereof|

---