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    • 专利摘要:
    herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxy-phenyl) pyridine-2-carboxylic acid or a derivative thereof and microtubule inhibiting herbicides . Synergistic herbicidal compositions containing (a) a compound of formula (1) are provided herein: 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-acid carboxylic acid or an agriculturally acceptable salt or ester thereof and (b) microtubule inhibiting herbicide, for example dimethenamid, dithiopyr, oryzaline, pendimethalin, propyzamide and thiazopyr or a derivative thereof. The methods and compositions provided herein provide control of undesirable vegetation, for example in direct seeded, water-seeded and transplanted rice crops, cereals, wheat, barley, oats, rye, sorghum, maize, sugar cane, sunflower. , rapeseed, canola, sugar beet, soybean, cotton, pineapple, grass herbs, grasslands, pastures, fallow, grass, tree and vine orchards, aquatic, planting, vegetables, industrial vegetation treatment (ivm) and rowdy work ).
    公开号:BR102013018481B1
    申请号:R102013018481-0
    申请日:2013-07-19
    公开日:2019-06-18
    发明作者:Carla Yerkes；Richard Mann；Norbert Satchivi
    申请人:Dow Agrosciences Llc；
    IPC主号:
    专利说明:

    Invention Patent Descriptive Report for HERBICIDIC COMPOSITIONS UNDERSTANDING 4-AMINO-3-CHLORINE-5-FLUORIC ACID (6- (4-CHLORINE-2-FLUORO-3-METOXY-FENYL) PYRIDINE-2-CARBOXYLIC OR A DERIVED FROM THE SAME AND HERBICIDES OF MICROTUBLE INHIBITION, AND METHOD FOR CONTROL OF UNDESIRABLE VEGETATION.
    Priority Claim [001] The present application claims the benefit of provisional patent application number US 61 / 675,100, filed on July 24, 2012, and patent application serial number US 13 / 840,303, filed on March 15, 2013 , whose descriptive report of each is incorporated here for reference in its entirety.
    Field [002] Herbicidal compositions comprising (a) 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic or an ester or salt thereof are provided here agriculturally acceptable and (b) a microtubule inhibiting herbicide. Also provided here are methods of controlling undesirable vegetation comprising application of (a) 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3methoxyphenyl) pyridine-2-carboxylic acid or an ester or the same agriculturally acceptable salt, and (b) a microtubule inhibiting herbicide. Background [003] The protection of crops against weeds and other vegetation that inhibit crop growth is a constantly recurring problem in agriculture. To help combat this problem, researchers in the field of synthetic chemistry have produced a wide variety of chemical agents and chemical formulations effective in controlling such unwanted growth. Chemical herbicides of many types have been revealed in the literature and a large number are in commercial use. However, there remains a need to compose
    Petition 870180158325, of 12/04/2018, p. 7/109
    2/94 tions and methods that are effective in controlling undesirable vegetation.
    Summary [004] Herbicidal compositions comprising a herbicidally effective amount of (a) a compound of Formula (I),


    or an agriculturally acceptable salt or ester thereof, and (b) a microtubule inhibiting herbicide. The compositions can also contain an agriculturally acceptable adjuvant or carrier.
    [005] Unwanted vegetation control methods are also provided here comprising applying (a) a compound of Formula (I) or an ester or salt of the same agriculturally acceptable and (b) a microtubule inhibiting herbicide.
    [006] Several modalities are mentioned below. In the modalities, the ratio of compound (a) to compound (b) can be expressed in units of weight to weight (g to g), gae / ha to gae / ha or gae / ha to gai / ha.
    1. A synergistic herbicidal composition comprising a herbicidally effective amount of (a) a compound of Formula (I)
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    or an agriculturally acceptable salt or ester thereof and (b) a microtubule inhibiting herbicide.
    2. The composition of modality 1, wherein (a) is a C1-C4 alkyl or benzyl ether of compound (I).
    3. The composition of modality 2, wherein (a) is a benzyl ester of compound (I).
    4. The composition of modality 1, where (a) is the compound of Formula (I), which is carboxylic acid.
    5. The composition of any one of the modalities 14, in which (b) is dimethenamide, S-dimethenamide, dithiopir, orizaline, pentimethalin, propizamide or thiazopyr.
    6. The composition of modality 1, wherein (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is dimethenamide or S-dimethenamide.
    7. The composition of modality 1, wherein (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester or (b) is dithiopir.
    8. The composition of modality 1, wherein (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is oryzaline.
    9. The composition of modality 1, where (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is pendimethalin.
    10. The composition of modality 1, in which (a) is the compound of Formula (I) or an benzyl ester agriculturally acceptable
    Petition 870180158325, of 12/04/2018, p. 9/109
    4/94 speed and (b) is propizarida.
    11. The composition of modality 1, wherein (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is thiazopyr.
    12. The composition of any of the modalities 111 further comprising a herbicide protector.
    13. The composition of modality 5, wherein the weight ratio of the compound of Formula (I) or salt or ester of the same agriculturally acceptable to dithiopir or salt or ester of the same agriculturally acceptable is from about 1: 3360 to about 1: 1 or from about 1: 400 to about 1: 100 or from about 1: 200 to about 1:50 or from about 1: 100 to 1: 35 or from about 1: 1 or from about 1: 2 or from about 1: 4 or from about 1: 8 or from about 1: 16 or from about 1:32 to about 1: 1 or from about 1:64 to 1: 1.
    14. The composition of modality 5, in which the weight ratio of the compound of Formula (I) or salt or ester of the same agriculturally acceptable to dimethenamide or S-dimethenamide or salt or ester of the same agriculturally acceptable is from about 1: 820 to about 3: 1 or from about 1: 400 to about 2.5: 1, from about 1: 300 to about 2: 1, from about 1: 200 to about 1.5: 1 and from about 1: 100 to about 1: 1.
    15. The composition of modality 5, wherein the weight ratio of the compound of Formula (I) or salt or ester of the same agriculturally acceptable to oryzaline or salt or ester of the same agriculturally acceptable is from about 1: 1120 to about 9: 1 or from about 1: 600 to about 7: 1 or from about 1: 500 to about 6: 1 or from about 1: 400 to about 5; 1 or from about 1: 300 to about 4: 1 or from about
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    1: 200 to about 3: 1, from about 1: 9, from about 1:16, from about 1:35, from about 1:64 or from about 1: 256 to about 1: 9.
    16. The composition of modality 5, in which the weight ratio of compound of Formula (I) or salt or ester of the same agriculturally acceptable to pendimethalin or salt or ester of the same agriculturally acceptable is from about from about 1: 1120 to about 3: 1, from about 1: 1000 to 2: 1, from about 1: 750 to about 1.5: 1, from about 1: 500 to about 1: 1, from about 1: 4, from about 1: 8, from about 1:16, from about 1:32, from about 1:64, from about 1: 128 and from about 1: 448 to 1: 2.
    17. The composition of modality 5, in which the weight ratio of the compound of Formula (I) or the agriculturally acceptable salt or ester thereof to propizamide or the agriculturally acceptable salt or ester thereof is from about 1: 600 to about 4: 1, from about 1: 500 to about 3: 1, from about 1: 400 to about 2: 1, from about 1: 300 to about 1: 1, from about 1: 9, from about 1:18, from about 1:32, from about 1:64, from about 1: 128 and from about 1: 140 to about 1: 2.2.
    18. The composition of modality 5, wherein the weight ratio of the compound of Formula (I) or salt or ester of the same agriculturally acceptable to thiazopyr or salt or ester of the same agriculturally acceptable is from about 1: 1120 to about 6: 1 or from about 1: 1000 to about 5: 1, from about 1: 500 to about 4; 1, from about 1: 400 to 3: 1, from about 1: 400 to 2: 1, from about 1: 200 to about 1: 1, from 1: 9, from 1:18, from from about 1:36, from from around
    Petition 870180158325, of 12/04/2018, p. 10/119
    6/94 from 1:72 and from about 1:10 to about 1:32.
    19. The composition of any of the modalities 118 further comprising an agriculturally acceptable adjuvant or carrier.
    20. The composition of any of the modalities 118, which is synergistic as determined by the Colby equation.
    21. An undesirable vegetation control method that comprises contact of the vegetation or its location with or application to soil or water to prevent the emergence or growth of vegetation in the composition of any of the modalities 1-20.
    22. Method of controlling undesirable vegetation, which comprises contact of vegetation or its location with or application to soil or water to prevent the emergence or growth of vegetation of a herbicidally effective amount of (a) a compound of Formula (I)
    or an agriculturally acceptable salt or ester thereof and (b) a microtubule inhibiting herbicide.
    23. The 21 or 22 modality method, where the method is practiced on at least one member of the group consisting of rice, cereals, wheat, barley, oats, rye, sorghum, corn, sugar cane, sunflower, rapeseed, canola , sugar beet, soy, cotton, pineapple, grass for pasture, grassland, pasture, fallow, grass, tree and vine orchards, aquatic, plantation crops, vegetables, industrial vegetation management (IVM) or easements (ROW) (Rlghts-of-Way).
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    7/94
    24. Method 21 or 22, in which the undesirable vegetation is immature.
    25. Method 21 or 22, in which (a) and (b) are applied to water.
    26. Method 25, in which the water is part of a flooded rice field.
    27. The 21 or 22 method, where (a) and (b) are applied pre-emergently to the weed or crop.
    28. The 21 or 22 modality method, where (a) or (b) are applied post-emergently to weed or crop.
    29. The 21 or 22 modality method, in which undesirable vegetation is controlled in glyphosate-tolerant plants, 5-enolpyruvylshiquime-3-phosphate (EPSP) synthase, glufosinate, glutamine synthetase inhibitor, dicamba, auxin phenoxy, pyridyloxy auxin, synthetic auxin, auxin transport inhibitor, aryloxyphenoxypropionate, cyclohexanedione, phenylpyrazole, acetyl CoA carboxylase inhibitor (ACCase), imidazolinone, sulfonylurea, pyrimidinylthiobenzoate, triazolpyrimidine sulfonamide, dimethylamine, pyridinimide, dimethyloxy acetohydroxy acid synthase (AHAS), 4-hydroxyphenylpyruvate dioxigenase (HPPD) inhibitor, phytene desaturase inhibitor, carotenoid biosynthesis inhibitor, protoporphyrinogen oxidase (PPO) inhibitor, cellulose biosynthesis inhibitor, mitosis inhibitor, mitosis inhibitor microtubule, very long-chain fatty acid inhibitor, lipid and acid biosynthesis inhibitor fatty acid, photosystem I inhibitor, photosystem II inhibitor, triazine or bromoxynil.
    30. The method of modality 29, in which the tolerant crop has multiple or stacked characteristics conferring resistance and / or tolerance to multiple herbicides or multiple modes of action.
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    8/94
    31. Method 21 or 22, where the undesirable vegetation comprises a herbicide-resistant or tolerant weed.
    32. The method of modality 21 or 22, in which the resistant or tolerant weed is a biotype with resistance or tolerance to multiple herbicides, multiple chemical classes, multiple herbicide modes or via multiple resistance mechanisms.
    33. The method of modality 31, in which the resistant or tolerant weed is a biotype resistant or tolerant to acetolactate synthase (ALS) or acetohydroxy acid synthase (AHAS) inhibitors, photosystem II inhibitors, acetyl CoA carboxylase inhibitors (ACCase) , synthetic auxins, auxin transport inhibitors, photosystem I inhibitors, 5-enolpyruvylshiquime-3 phosphate synthase (EPSP) inhibitors, microtubule assembly inhibitors and fatty acid and lipid synthesis inhibitors, oxygen protoporphyrinogen (PPO) inhibitors, carotenoid biosynthesis inhibitors, very long chain fatty acid (VLCFA) inhibitors, phytene desaturase (PDS) inhibitors, glutamine synthetase inhibitors, 4-hydroxyphenyl-pyruvate-dioxigenase (HPPD) inhibitors, mitosis inhibitors, cellulose biosynthesis, multiple mode-of-action herbicides, quinclorak, arylaminopropionic acids, difenzoquate, endothal or organoarsenic acids.
    34. The composition of any one of embodiments 15, wherein the weight ratio of the compound of Formula (I) or salt or ester of the same agriculturally acceptable to dithiopir or salt or ester of the same agriculturally acceptable is from about 1 : 3360 at about 1: 1.
    35. The composition of any one of embodiments 15, wherein the weight ratio of the compound of Formula (I) or salt or ester
    Petition 870180158325, of 12/04/2018, p. 10/149
    9/94 of the same agriculturally acceptable for dimethenamide or Sdimetenamide or salt or ester of the same agriculturally acceptable is from about 1: 820 to about 3: 1.
    36. The composition of any one of embodiments 15, wherein the weight ratio of the compound of Formula (I) or salt or ester of the same agriculturally acceptable oryzaline or salt or ester of the same agriculturally acceptable is from about 1 : 1120 to about 9: 1.
    37. The composition of any of the modalities 15, wherein the weight ratio of the compound of Formula (I) or salt or ester of the same agriculturally acceptable to pendimethalin or salt or ester of the same agriculturally acceptable is from about 1 : 1120 to about 3: 1.
    38. The composition of any of the modalities 15, wherein the weight ratio of the compound of Formula (I) or salt or ester of the same agriculturally acceptable to propizamide or salt or ester of the same agriculturally acceptable is from about 1 : 600 to about 4: 1.
    39. The composition of any of the modalities 15, wherein the weight ratio of the compound of Formula (I) or salt or ester of the same agriculturally acceptable thiozapyr or salt or ester of the same agriculturally acceptable is from about 1 : 1120 to about 6: 1.
    Detailed Description
    DEFINITIONS [007] As used herein, the compound of Formula (I) has the following structure:
    Petition 870180158325, of 12/04/2018, p. 10/159
    10/94 nh 2
    Cl
    OH
    H3C / O (I) [008] The compound of Formula (I) can be identified by the name 4-amino-3-chloro-6- (4-chloro-2-fluoro-3-methoxyphenyl) -5-fluorpiridine- 2carboxylic and has been 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 control of undesirable vegetation, including grass, broadleaf weeds and sedge, in situations of non-culture and multiple culture.
    [009] As used herein, microtubule inhibiting herbicides are herbicides that inhibit cell division through binding with tubulin and interfering with the formation of microtubules.
    [0010] Exemplary microtubule inhibiting herbicides include, but are not limited to, dimethenamide, dithiopir, oryzaline, pendimethalin, propizamide and thiazopyr or a salt, carboxylic acid, carboxylate salt or ester of the same agriculturally acceptable.
    [0011] As used herein, dimethenamide is (RS) -2-chloro-M- (2,4-dimethyl-3-thienyl) -M- (2-methoxy-1-methylethyl) acetamide and has the following structure:
    Cl [0012] The S-isomer, that is, (S) -2-chloro-N- (2,4-dimethyl-3-thienyl) -N- (2-methoxy-1-methylethyl) acetamide has also been used as a herbicide . The herbicidal activity for dimethenamide is exemplified in Tomlina, C., ed., A World Compendlum The Pestle Manual. 15 th ed.
    Petition 870180158325, of 12/04/2018, p. 10/169
    11/94
    Alton: BCPC Publications, 2009 (hereafter The Pesticide Manual, Fifteenth Edition, 2009.). Exemplary uses of dimethenamide include its use for pre- or post-emergence control of annual ryegrass and broadleaf weeds, for example, in crops of maize, soybeans, sugar beet, potatoes, dried beans and other crops.
    [0013] As used herein, dithiopir is S, S'-dimethyl-2- (difluormethyl) 4- (2-methylpropyl) -6- (trifluormethyl) -3,5-pyridinecarbothioate and has the following structure:
    [0014] Its herbicidal activity is exemplified in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of dithiopir include its use for pre-emergence or post-emergence control of annual ryegrass or broadleaf weeds, for example, in grass.
    [0015] As used here, oryzaline is 4- (dipropylamino) -3,5dinitrobenzenesulfonamide and has the following structure:
    [0016] Its herbicidal activity is exemplified in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of oryzaline include its use for pre-emergence control of annual ryegrass and small-leaved weeds, for example, in fruit trees, walnut trees, vines, ornamentals, soybeans, berries,
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    12/94 gram of amenity and non-crop areas.
    [0017] As used here, pendimethalin is M- (1-ethylpropyl) -3,4dimethyl-2,6-dinitrobenzenamine and has the following structure:
    [0018] Its herbicidal activity is exemplified in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of pendimethalin include its use for pre-plant, pre-emergence, pre-transplant or early post-emergence control of annual ryegrass and broadleaf weeds annual, for example, in rice, soybeans and orchards of tree and videria.
    propizamide [0019] As used herein, thiazopyr is 2- (difluormethyl) -5- (4,5-hydroxy-2-thiazolyl) -4- (2-methylpropyl) -6- (trifluoromethyl) -3-pyridinecarboxylate and presents the structure that follows:
    [0020] Its herbicidal activity is exemplified in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of tiazopir include its use for pre-emergence control of annual ryegrass and some broadleaf weeds, for example, in fruit trees, vines, citruses, sugar cane, pineapples, alfalfa and forestry.
    [0021] As used herein, herbicide means a compound, for example, an active ingredient that kills, controls, or otherwise adversely modifies the growth of plants.
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    13/94 [0022] As used herein, an herbicidally effective or vegetation control amount is an amount of active ingredient that causes an adverse modification effect on the vegetation, for example, causing deviations from natural development, killing, making regulation, causing dissection, causing delay and similar.
    [0023] As used herein, control of undesirable vegetation means prevention, reduction, death or otherwise adversely modifying the development of plants and vegetation. Methods for controlling undesirable vegetation by applying certain herbicidal combinations or compositions are described here. Application methods include, but are not limited to, applications to the vegetation or its location, for example, application to the area adjacent to the vegetation, as well as pre-emergence, post-emergence, leaf (spread, directed, band, point, mechanic , over or rescue) and applications in water (emergent or submerged vegetation, scattered, dot, mechanical, injected in water, scattered granular, dot granular, agitator bottle or spray with flow), application methods by hand, backpack, machine , tractor or aerial (airplane or helicopter).
    [0024] As used herein, plants and vegetation include, but are not limited to, germinating seeds, emerging seedlings, plants emerging from vegetative propagules, immature vegetation and established vegetation.
    [0025] As used herein, agriculturally acceptable salts and esters refer to salts and esters that exhibit herbicidal activity or that are or can be converted to plants, water or soil in said herbicide. Exemplary agriculturally acceptable esters are those that are or can be hydrolyzed, oxidized, metabolized or otherwise converted, for example, into plants, water or
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    14/94 soil, in the corresponding carboxylic acid which, depending on the pH, can be in dissociated or non-dissociated form.
    [0026] 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 aluminum cations of Formula:
    R 1 R 2 R 3 R 4 N + 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 of which is 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 2 and R 4 together can represent an aliphatic difunctional portion 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 hydroxide of tetraalkylammonium, such as tetramethylammonium hydroxide or choline hydroxide.
    Exemplary esters include those derived from C1-C12 alkyl, C3-C12 alkenyl, C3-C12 alkynyl or C7-C10 alkyl alcohols substituted with alkyl, such as methyl alcohol, isopropyl alcohol, 1-butane, 2- ethylexanol, butoxyethanol, methoxypropanol, allyl alcohol, propargyl alcohol, cyclohexanol or benzyl alcohols not substituted or substituted. Benzyl alcohols can be substituted with from 1-3 substituents independently selected from halogen, C1-C4 alkyl or C1-C4 alkoxy. Esters can be prepared by coupling the acids with the alcohol using any number of suitable activating agents such as those used
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    15/94 for peptide couplings such as dicyclohexylcarbodiimide (DCC) or carbonyl diimidadzol (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 [0028] Herbicidal compositions are provided herein comprising a herbicidally effective amount of (a) a compound of Formula (I)
    or an agriculturally acceptable salt or ester thereof and (b) a microtubule inhibiting herbicide. In some embodiments, the microtubule inhibiting herbicide is dimethenamide, dithiopir, oryzaline, pendimethalin, propizamide and thiazopyr or a salt, carboxylic acid, carboxylate salt or ester of the same agriculturally acceptable.
    [0029] Unwanted vegetation control methods are also provided here by contacting the vegetation or its location, or area adjacent to the vegetation, with or applying to the soil or water to prevent the emergence or growth of vegetation a herbicidally effective amount of the Formula compound (I) or salt or ester of the same agriculturally acceptable and (b) microtubule inhibiting herbicide. In certain embodiments, the methods employ the compositions described here.
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    16/94 [0030] Still, in some embodiments, the combination of compound (I) or salt or ester of the same agriculturally acceptable and microtubule inhibiting herbicides, or a salt or ester of the same agriculturally acceptable, exhibits synergism, for example, the herbicidal active ingredients are more effective in combination than when applied individually. Synergism can be defined as an interaction of two or more factors so that the effect when combined is greater than the predicted effect based on the response of each factor applied separately. Senseman, S., ed. Herbicide Handbook. 9 th ed. Lawrence: Weed Science Society of America, 2007. In certain embodiments, compositions exhibit synergy as determined by the Colby equation, SR 1967. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 15: 20-22.
    [0031] In certain embodiments of the compounds and methods described here, the compound of Formula (I), that is, carboxylic acid, is employed. In certain embodiments, a carboxylate salt of the compound of Formula (I) is employed. In certain embodiments, an aralkyl or alkyl ester is employed. In certain embodiments, a benzyl, substituted benzyl or C1-C4 alkyl ester, for example, of n-butyl, is employed.
    [0032] In some embodiments, the compound of Formula (I) or salt or ester thereof and dimethenamide, dithiopir, oryzaline, pentimethalin, propizamide and thiazopyr, or an agriculturally acceptable salt, carboxylic acid, carboxylate salt or ester thereof are formulated in a composition, mixed in a tank, applied simultaneously or applied sequentially.
    [0033] 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 species of plant to be controlled, the growth stage of the plant, the countries
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    17/94 dilution application parameters and spray droplet size, particle size of solid components, environmental conditions at the time of use, specific compound used, specific adjuvants and carriers used, type of soil and similar , as well as the amount of chemical agent 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 water application to flooded rice fields or bodies of water (for example, ponds, lakes and streams), to relatively immature undesirable vegetation to obtain control maximum weeds.
    [0034] In some embodiments, the compositions and methods provided here are used to control weeds in crops, including, but not limited to, no-till rice, sown in water and transplanted, cereals, wheat, barley, oats, rye , sorghum, corn, sugar cane, sunflower, rapeseed, canola, sugar beet, soy, cotton, pineapple, grass for pasture, grassland, pasture, fallow, grass, tree and vine orchards, aquatic, plantation crops, plant management, industrial vegetation management (IVM) or easements of passage (ROW).
    [0035] In certain embodiments, the compositions and methods provided here are used to control weeds in rice. In certain modalities, rice is direct sown rice, water-sown or transplanted rice.
    [0036] The compositions and methods described here can be used to control undesirable vegetation in glyphosate-tolerant crops, tolerant to 5-enolpyruvylshiquimate-3-phosphate (EPSP) synthase, tolerant to glufosinate, tolerant to glutamine synthase inhibitor, tolerant to dicamba, tolerant to phenoxy auxin, tolerant to
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    18/94 pyridyloxy auxin, auxin tolerant, tolerant to auxin transport inhibitor, tolerant to aryloxyphenoxypropionate, tolerant to cyclohexanedione, tolerant to phenylpyrazoline, tolerant to acetyl CoA carboxylase inhibitor (ACCase), tolerant to imidazolinone, tolerant to sulfonylurea pyrimidinylthiobenzoate, tolerant to triazolpyrimidine, tolerant to sulfonylaminocarbonyltriazolinone, tolerant to acetolactate synthase (ALS) or tolerant to acetohydroxy acid synthase (AHAS) inhibitor, tolerant to 4-hydroxyphenyl-pyruvate inhibitor, dichloride inhibitor (HPP) , tolerant to carotenoid biosynthesis inhibitor, 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 lipid and fatty acid biosynthesis inhibitor, tolerant to photosystem inhibitor I, tolerant to photosystem inhibitor II, tolerant to triazine or bromoxynil (such as, but not limited to, soy, cotton, canola, rapeseed, rice, cereals, corn, sorghum, sunflower, sugar beet, sugar cane sugar, gram, etc.), for example, in conjunction with glyphosate, EPSP synthase inhibitors, glufosinate, glutamine synthase inhibitors, dicamba, phenoxy auxins, pyridyloxy auxins, synthetic auxins, auxin transport inhibitors, aryloxyphenoxypropionates, cyclohexanediones, phenylpyrazolines, ACCase inhibitors, imidazolinones, sulfonylureas, pyrimidinylthiobenzoates, triazolpyrimidines, sulfonylaminocarbonyltriazolinones, ALS or AHAS inhibitors, HPPD inhibitors, phytene desaturase inhibitors, inhibitors of carotene biosynthesis, carotene biosynthesis inhibitors, carotene biosynthesis inhibitors , microtubule inhibitors, very long chain fatty acid inhibitors, acid biosynthesis inhibitors fatty acid and lipid, photosystem I inhibitors, photosystem II inhibitors, triazines and bromoxynil. Compositions and methods can be used in vegetable control
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    19/94 undesirable in cultures having multiple or stacked characteristics giving tolerance to multiple chemicals and / or inhibitors of multiple modes of action. In some embodiments, the compound of Formula (I) or salt or ester of the same and herbicide or salt or ester of the same complement are used in combination with herbicides that are selective for the crop being treated and that complement the controlled weed spectrum by these compounds at the application rate employed. In some embodiments, the compositions described here and other complementary herbicides are applied at the same time, either as a combination formulation, as a tank mixture or sequentially. Compositions and methods can be used to control undesirable vegetation in crops having tolerance to agronomic stress (including, but not limited to, drought, cold, heat, salt, water, nutrient, fertility, pH), tolerance to plague (including , but not limited to, insects, fungi and pathogens) and crop improvement characteristics (including, but not limited to, yield; protein; carbohydrate or oil content; protein, carbohydrate or oil composition; plant stature and architecture of plant).
    [0037] The compositions and methods provided here are used to control undesirable vegetation. Undesirable vegetation includes, but is not limited to, undesirable vegetation that occurs in rice, cereals, wheat, barley, oats, rye, sorghum, corn, sugar cane, sunflower, rapeseed, canola, sugar beet, soy, cotton, pineapple, pasture, grassland, pasture, fallow, grass, tree and vine orchards, ornamental, aquatic species, plantation crops, vegetables or non-culture environments (eg easements (ROW), industrial vegetation management (IVM ).
    [0038] In some embodiments, the methods provided here are used to control undesirable vegetation in rice. In certain modalities, the undesirable vegetation is Brachiaria platyphylla (Gro
    Petition 870180158325, of 12/04/2018, p. 10/25
    20/94 seb) Nash or Urochloa platyphylla (Nash) R.D. Webster (broadleaf signalgrass), BRAPP), Digitaria sanguinalis (L.) Scop. (large crabgrass), DIGSA), Echinochloa species (ECHSS), Echinochloa crus-galli (L.) P. Beauv. (barnyardgrass), ECHCG), Echinochloa crus-pavonis (Kunth) Schult. (rice grass (gulf cockspur), ECHCV), Echinochloa colonum (L.) LINK (colony grass (junglerice), ECHCO), Echinochloa oryzoides (Ard.) Fritsch (early watergrass) , ECHOR), Echinochloa oryzicola (Vasinger) Vasinger (late watermilk, ECHPH), Echinochloa phyllopogon (Stapf) Koso-Pol. (rice barnyardgrass), ECHPH), Echinochloa polystachya (Kunth) Hitchc. (creeping river grass, ECHPO), Ischaemum rugosum Salisb. (male grass (saramollagrass), ISCRU), Leptochloa chinensis (L.) Nees (Chinese spring top (Chinese sprangletop), LEFCH), Leptochloa fascicularis (Lam.) Gray (bearded sprangletop, LEFFA), Leptochloa panicoides (Presl. ) Hitchc. (Amazon sprangletop, LEFPA), Oryza species (red and weedy rice), ORYSS), Panicum dichotomiflorum (L.) Michx. (bathed grass (fali panicum), PANDI), Paspalum dilatatum Poir. (honeygrass (dallisgrass), PASDI), Rottboellia cochinchinensis (Lour.) WD Clayton (camalote grass (itchgrass), ROOEX), Cyperus species (CYPSS), Cyperus difformis L. (small flower flatsedge), CYPDI), Cyperus dubius Rottb. (MAPDU), Cyperus esculentus L. (yellow nutsedge), CYPES), Cyperus would L. (rice flatsedge, CYPIR), Cyperus rotundus L. (purple nutsedge), CYPRO ), Cyperus serotinus Rottb./CBClarke (tidalmarsh flatsedge, CYPSE), Eleocharis (ELOSS), Fimbristylis miliacea (L.) Vahl (globe fringerush), FIMMI), Schoenoplectus (SCPSS), Schoenoplectus juncoides Roxb. (Japanese bulrush, SCPJU), Bolboschoenus
    Petition 870180158325, of 12/04/2018, p. 10/26
    21/94 maritimus (L.) Palla or Schoenoplectus maritimus L. Lye (sea reed (sea clubrush), SCPMA), Schoenoplectus mucronatus L. (reed-doarrozal (ricefield bulrush), SCPMU), species Aeschynomene (angiquinho (angiquinho ( jointvetch), AESSS), Alternanthera philoxeroides (Mart.) Griseb. (alligatorweed, ALRPH), Alisma plantagoaquatica L. (common water plantain), ALSPA), Amaranthus species (chenopods and amaranths (pigweeds and amaranths), AMASS), Ammannia coccinea Rottb . (red stem), AMMCO), Commelina benghalensis L. (trapoeraba (Benghal dayflower), COMBE), Eclipta alba (L.) Hassk. (American false daisy, ECLAL), Heteranthera limosa (SW.) Willd./Vahl (water hyacinth (ducksalad), HETLI), Heteranthera reniformis R. & P. (water hyacinth (roundleaf mudplantain), HETRE) , Ipomoea species (morning glory, IPOSS), Ipomoea hederacea (L.) Jacq. (jeticuçu (ivyleaf morningglory), IPOHE), Lindernia dubia (L.) Pennell (low false pimpernel), LIDDU), Ludwigia species (LUDSS), Ludwigia linifolia Poir. (southeastern primrose-willow, LUDLI), Ludwigia octovalvis (Jacq.) Raven (longfruited primrose-willow, LUDOC), Monochoria korsakowii Regel & Maack (monochoria), MOOKA), Monochoria vaginalis (Burm. F.) C. Presl ex Kuhth, (monorail (monorail), MOOVA), Murdannia nudiflora (L.) Brenan (trapoerabinha (doveweed), MUDNU), Polygonum pensylvanicum L., (Pennsylvania smartweed, POLPY), Polygonum persicaria L. (herb-of-bug) (ladysthumb), POLPE), Polygonum hydropiperoides Michx. (POLHP, mild smartweed), Rotala indica (Willd.) Koehne (Indian toothcup, ROTIN), Sagittaria species, (duckhead (arrowhead), SAGSS), Sesbania exaltata (Raf.) Cory / Rydb. Ex Hill (sesbania (hemp sesbania), SEBEX) or Sphenoclea zeylanica Gaertn. (majuba (gooseweed), SPDZE).
    [0039] In some embodiments, the methods provided here are used to control undesirable vegetation on cereals. In certain
    Petition 870180158325, of 12/04/2018, p. 10/279
    22/94 modalities, the undesirable vegetation is Alopecurus myosuroides Huds. (blackgrass), ALOMY), Apera spica-venti (L.) Beauv. (silky feathergrass (windgrass), APESV), Avena fatua L. (wild oat), AVEFA), Bromus tectorum L. (bromovassoura (downy brome), BROTE), Lolium multiflorum Lam. (Italian ryegrass ( Italian ryegrass), LOLMU), Phalaris minor Retz. (littleseed canarygrass, PHAMI), Poa annua L. (annual blue grass (annual bluegrass), POANN), Setaria pumila (Poir.) Roemer & JA Schultes (yellow foxtail), SETLU), Setaria viridis (L .) Beauv. (green foxtail), SETVI), Amaranthus retroflexus L. (red-root chenopod (redroot pigweed), AMARE), Brassica species (BRSSS), Brassica napus (winter rapeseed), BRSNW ), Chenopodium album L. (common lambsquarters), CHEAL), Cirsium arvense (L.) Scop. (Canadian thistle (Canada thistle), CIRAR), Galium aparine L. (catchweed bedstraw), GALAP), Kochia scoparia (L.) Schrad. (kochia, KCHSC), Lamium purpureum L. (dead nettle (purple deadnettle), LAMPU), Matricaria recutita L. (wild chamomile), MATCH), Matricaria matricarioides (Less.) Porter (pineapple herb (pineappleweed) , MATMT), Papaver rhoeas L. (common poppy), PAPRH), Polygonum convolvulus L. (wild buckwheat), POLCO), Salsola tragus L. (Russian thistle), SASKR), species Sinapis (SINSS), Sinapis arvensis L. (wild mustard), SINAR), Stellaria media (L.) Vill. (common chickweed, STEME), Veronica Persian Poir. (Persian speedwell), VERPE), Viola arvensis Murr. (field violet), VIOAR) or Viola tricolor L. (wild violet, VIOTR).
    [0040] In some embodiments, the methods provided here are used to control undesirable vegetation on pasture and pasture,
    Petition 870180158325, of 12/04/2018, p. 10/28
    23/94 fallow, IVM and ROW. In certain modalities, the undesirable vegetation is Ambrosia artemisiifolia L. (common ragweed), AMBEL), Cassia obtusifolia (sickle pod), CASOB), Centaurea maculosa auct. non Lam. (spotted knapweed, CENMA), Cirsium arvense (L.) Scop. (Canadian thistle (Canada thistle), CIRAR), Convolvulus arvensis L. (field bindweed), CONAR), Daucus carota L. (wild carrot), DAUCA), Euphorbia esula L. (euphorbia leafy spurge, EPHES), Lactuca serriola L./Torn. (prickly lettuce), LACSE), Plantago lanceolata L. (sheep tongue (buckhorn plantain), PLALA), Rumex obtusifolius L. (cow tongue (broadleaf dock), RUMOB), Sida spinosa L (thorn guanxuma (prickly sida), SIDSP), Sinapis arvensis L. (wild mustard), SINAR), Sonchus arvensis L. (perennial thistle (SONW), SONAR), Solidago species (varade- gold (goldenrod), SOOSS), Taraxacum officinale GH Weber ex Wiggers (dandelion), TAROF), Trifolium repens L. (white clover), TRFRE) or Urtica dioica L. (common nettle), URTDI).
    [0041] In some embodiments, the methods provided here are used to control undesirable vegetation found in row crops, tree and vine crops and perennial crops. In certain embodiments, the undesirable vegetation is Alopecurus myosuroides Huds. (foxgrass, ALOMY), Avena fatua L. (wild oat), AVEFA), Brachiaria decumbens Stapf. or Urochloa decumbens (Stapf) R.D. Webster (Suriname grass (Surinam grass), BRADC), Brachiaria brizantha (Hochst. ex A. Rich.) Stapf. or Urochloa brizantha (Hochst. ex A. Rich.) RD (beard grass), BRABR), Brachiaria platyphylla (Groseb.) Nash or Urochloa platyphylla (Nash) RD Webster (taquarinha (broadleaf signalgrass), BRAPP), Brachiaria plantaginea (Link) Hitchc. or Urochloa plantaginea
    Petition 870180158325, of 12/04/2018, p. 10/29
    24/94 (Link) R.D. Webster (marmalade grass (alexandergrass), BRAPL), Cenchrus echinatus L. (southern sandbur, CENEC), Digitaria horizontalis Willd. (Jamaica mattress grass (Jamaican crabgrass), DIGHO), Digitaria insularis (L.) Mez ex Ekman (sourgrass), TRCIN), Digitaria sanguinalis (L.) Scop. (large crabgrass), DIGSA), Echinochloa crus-galli (L.) P. Beauv. (barnyardgrass), ECHCG), Echinochloa colonum (L.) Link (colony grass (junglerice), ECHCO), Eleusine indica (L.) Gaertn. (goosegrass grass, ELEIN), Lolium multiflorum Lam. (Italian ryegrass (Italian ryegrass), LOLMU), Panicum dichotomiflorum Michx. (fall panicum), PANDI), Panicum miliaceum L. (millet (wild-prose millet), PANMI), Setaria faberi Herrm. (giant foxtail), SETFA), Setaria viridis (L.) Beauv. (green foxtail, SETVI), Sorghum halepense (L.) Pers. (Johnson grass (Johnsongrass), SORHA), Sorghum bicolor (L.) Moench ssp. Arundinaceum (sweet sorghum (shattercane), SORVU), Cyperus esculentus L. (yellow nutsedge), CYPES), Cyperus rotundus L. (purple nutsedge), CYPRO), Abutilon theophrasti Medik. (velvet leaf (velvetleaf), ABUTH), Amaranthus species (kenopodia and amaranths), AMASS), Ambrosia artemisiifolia L. (common ragweed), AMBEL), Ambrosia psilostachya DC. (western ragweed), AMBPS), Ambrosia trifida L. (giant ragweed), AMBTR), Anoda cristata (L.) Schlecht. (spurred anoda mallow, ANVCR), Asclepias syriaca L. (common milkweed), ASCSY), Bidens pilosa L. (hairy beggarticks), BIDPI), Borreria species (BOISS), Borreria alata (Aubl .) DC. or Spermacoce alata Aubl. (broadleaf buttonweed), BOILF), Spermacose latifolia (broadleaved button weed), BOILF), Chenopodium album L.
    Petition 870180158325, of 12/04/2018, p. 10/30
    25/94 common (common lambsquarters), CHEAL), Cirsium arvense (L.) Scop. (Canadian thistle (Canada thistle), CIRAR), Commelina benghalensis L. (comelina (tropical spiderwort), COMBE), Datura stramonium L. (trumpet (jimsonweed), DATST), Daucus carota L. (wild carrot), DAUCA), Euphorbia heterophylla L. (wild poinsettia), EPHHL), Euphorbia hirta L. or Chamaesyce hirta (L.) Millsp. (garden spurge, EPHHI), Euphorbia dentata Michx. (toothed spurge, EPHDE), Erigeron bonariensis L. or Conyza bonariensis (L.) Cronq. (hairy fleabane), ERIBO), Erigeron canadensis L. or Conyza canadensis (L.) Cronq. (Canadian fluff), Conyza sumatrensis (Retz.) EH Walker (tall fleabane), ERIFL), Helianthus annuus L. (common sunflower), HELAN), Jacquemontia tamnifolia (L. ) Griseb. (small leaf morningglory), IAQTA), Ipomoea hederacea (L.) Jacq. (jeticuçu (ivyleaf morningglory), IPOHE), Ipomoea lacunosa L. (white morning glory, IPOLA), Lactuca serriola L./Torn. (prickly lettuce), LACSE), Portulaca oleracea L. (common purslane), POROL), Richardia species (pusley, RCHSS), Sida species (sida, SIDSS), Sida spinosa L. (guanxuma-de , SIDSP), Sinapis arvensis L. (wild mustard, SINAR), Solanum ptychanthum Dunal (eastern black nightshade), SOLPT), Tridax procumbens L. (bull's grass (coat buttons ), TRQPR) or Xanthium strumarium L. (common cocklebur), XANST).
    [0042] In some embodiments, the methods provided here are used to control unwanted grass vegetation. In certain modalities, the undesirable vegetation is Bellis perennis L. (English daisy), BELPE), Cyperus esculentus L. (yellow nutsedge), CYPES), Cyperus species (CYPSS), Digitaria
    Petition 870180158325, of 12/04/2018, p. 10/31
    26/94 sanguinalis (L.) Scop. (large crabgrass), DIGSA), Diodia virginiana L. (Virginia buttonweed, DIQVI), species Euphorbia (euphorbia (spurge), EPHSS), Glechoma hederacea L. (ground ivy), GLEHE), Hydrocotyle umbellata L. (acariçoba (dollarweed), HYDUM), Kyllinga species (junquinho (kyllinga), KYLSS), Lamium amplexicaule L. (nettle (henbit), LAMAM), Murdannia nudiflora (L.) Brenan (trapoerabinha (doveweed) , MUDNU), Oxalis species (wood sorrel), OXASS), Plantago major L. (plantain (broadleaf plantain), PLAMA), Plantago lanceolata L. (sheep tongue (buckhorn / narrowleaf plantain), PLALA) , Phyllanthus urinaria L. (chamberbitter), PYLTE), Rumex obtusifolius L. (broadleaf dock, RUMOB), Stachys floridana Shuttlew. (Florida betony, STAFL), Stellaria media (L.) Vill. (common chickweed, STEME), Taraxacum officinale G.H. Weber ex Wiggers (dandelion (dandelion), TAROF), Trifolium repens L. (white clover), TRFRE) or Viola species (wild violet), VIOSS).
    [0043] In some embodiments, the compositions and methods provided here are used to control undesirable vegetation consisting of grass, broadleaf weeds and sedge. In certain embodiments, the compositions and methods provided are used to control undesirable vegetation including Amaranthus, Brachiaria or Urochloa, Chenopodium, Cirsium, Cyperus, Digitaria, Echinochloa, Ipomoea, Kochia, Lamium, Leptochloa, Papaver, Schoenoplectus, Sesbania, Setaria, Sinapis , Stellaria and Xanthium.
    [0044] In some embodiments, the combination of compound (I) or ester or salt of the same agriculturally acceptable and microtubule inhibiting herbicides or salt or ester of the same agriculturally acceptable is used to control Amaranthus retroflexus L. (red root kenopodium ( redroot pigweed), AMARE), Brachiaria platyphylla (Gri
    Petition 870180158325, of 12/04/2018, p. 10/32
    27/94 seb.) Nash or Urochloa platyphylla (Nash) RD Webster (taquarinha (broadleaf slgnalgrass), BRAPP), Brasslca napus (winter rapeseed (wlnter rapeseed), BRSNW), Chenopodlum album L. (common anthracite (common lambsquarters ), CHEAL), Clrslum arvense (L.) Scop. (Canadian thistle (Canada thlstle), CIRAR), Cyperus esculentus L. (yellow nutsedge), CYPES), Cyperus dlfformls L. (blackbird (smallflower umbrella sedge), CYPDI), Cyperus rotundus L. (purple nutsedge) nutsedge), CYPRO), Digitaria sangulnalls (L.) Scop. (large crabgrass), DIGSA), Echlnochloa crus-galll (L.) Beauv. (ricegrass (barnyardgrass), ECHCG), Echlnochloa colona (L.) Link (colonygrass (junglerlce), ECHCO), Echlnochloa oryzoldes (Ard.) Fritsch (early watergrass), ECHOR), Ipomoea hederacea Jacq. (jeticuçu (lvyleaf mornlngglory), IPOHE), Kochla scoparla (L.) Schrad. (kochia, KCHSC), Lamlum purpureum L. (dead nettle (purple deadnettle), LAMPU), Leptochloa chlnensls (L.) Nees (Chinese spring top (Chlnese sprangletop), LEFCH), Papaver rhoeas L. (common poppy poppy), PAPRH), choenoplectus juncoldes (Roxb.) Palla (Japanese bulrush), Sesbanla exaltata (Raf.) Cory / Rydb. Ex Hill (hemp sesbania, SEBEX), Setarla faberl Herrm. (giant foxtail (glant foxtall), SETFA), Slnapls arvensls L. (wild mustard (wlld mustard), SINAR), Stellarla medla (L.) Vill. (common morugem (common chlckweed), STEME) and Xanthlum strumarlum L. (common thistle (common cocklebur), XANST).
    [0045] The compounds of Formula I or salt or ester of the same agriculturally acceptable can be used to control herbicide resistant or tolerant weeds. The methods employing the combination of a Formula I compound or an agriculturally acceptable salt or ester thereof and the compositions described here can also be employed to control resistant weeds.
    Petition 870180158325, of 12/04/2018, p. 10/33
    28/94 herbicide tolerant or tolerant. 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 (eg, imidazolinones, sulfonylureas, pyrimidinylthiobenzoates, dimethoxy-pyrimidines, triazolpyramines , sulfonylaminocarbonyltriazo-linones), photosystem II inhibitors (for example, phenylcarbamates, pyridazoninones, triazines, triazinones, uracils, amides, ureas, benzothiazinones, nitriles, phenylpyridazine), acetyl CoA carboxyloxide (ACASE) inhibitors, (ACASE) cyclohexanediones, phenylpyrazolines), synthetic auxins (eg benzoic acids, phenoxycarboxylic acids, pyridine carboxylic acids, quinoline carboxylic acids), auxin transport inhibitors (eg phthalates, semicarbazones), photosystem I inhibitors (eg bipyridyls), 5enolpyruvylshiquime-3-phosphat inhibitors o (EPSP) (eg glyphosate), glutamine synthetase inhibitors (eg glufosinate, bialaphos), microtubule assembly inhibitors (eg benzamides, benzoic acids, dinitroanilines, phosphoramidates, pyridines), mitosis inhibitors (eg carbamates), very long chain fatty acid (VLCFA) inhibitors (eg acetamides, chloroacetamides, oxyacetamides, tetrazolinones), fatty acid and lipid synthesis inhibitors, protoporphyrinogen oxidase (PPO) inhibitors (eg diphenyl ethers) , N-phenylphthalimides, oxadiazoles, oxazolidinediones, phenylpyrazoles, pyrimidinedione, thiadiazoles, triazolinones), carotenoid biosynthesis inhibitors (for example, clomazone, amitrol, aclonifene), phytene desaturase (ammonia) inhibitors (ammonia) , phenoxybutan-amides, pyridiazinones, pyridines), 4-hydroxyphenyl-pyruvate-dioxigenase (HPPD) inhibitors (for example, calistemones, isoxazoles, pyrazoles, tricetones, inhibitors idents of cellulose biosynthesis (eg nitriles, benzamides, quinclorak, triazolcarb
    Petition 870180158325, of 12/04/2018, p. 10/34
    29/94 xamides), herbicides with multiple modes of action such as quinclorak and unclassified herbicides such as arylaminopropionic, difenzoquate, endothal and organoarsenic acids. 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 herbicide modes of action and biotypes with multiple resistance or tolerance mechanisms (for example, target site resistance or metabolic resistance).
    [0046] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or salt or ester thereof is used in combination with dimethenamide or a separate isomer, for example, its S isomer. in some embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof or dimethenamide or an isomer separate from it is within the range of from about 1: 820 to about 3: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to dimethenamide or an isomer separated therefrom is within the range of from about 1: 545 to about 1: 2. In certain embodiments, the compositions comprise the compound of Formula (I) or its benzyl or n-butyl ester and dimethenamide or a separate isomer. With respect to methods, in certain modalities, the methods comprise contact of undesirable vegetation or its location or application to soil or water to prevent the emergence or growth of vegetation by a composition described here. In some embodiments, the composition is applied at an application rate of from about 102 grams of active ingredient per hectare (g ai / ha) to about 1940 g ai / ha based on the total amount of active ingredients in the composition . In certain modalities, the composition is applied at an application rate from
    Petition 870180158325, of 12/04/2018, p. 10/35
    30/94 from about 105 grams of active ingredient per hectare (g ai / ha) to about 1250 g ai / ha based on the total amount of active ingredients in the composition. In some embodiments, the methods comprise contact of the unwanted vegetation or location of the same or application to the soil or water to prevent the emergence or growth of vegetation with a compound of Formula (I) or salt or ester thereof in dimethenamide or an isomer separated from the same, for example, sequentially or simultaneously. In some embodiments, dimethenamide or an isomer separated from it is applied at a rate of from about 100 g ai / ha to about 1640 g ai / ha and the compound of Formula (I) of salt or ester thereof is applied at a rate from about 2 g ae / ha to about 300 g ae / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl or n-butyl ester and dimethenamide or a separate isomer.
    [0047] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or salt or ester thereof is used in combination with dithiopir or salt of the same agriculturally acceptable. With respect to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to dithiopir is within the range of from 1: 1120 to about 9: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to dithiopir is within the range of from about 1:32 to about 1: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to dithiopir is within the range of from about 1: 1 to about 1:64. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to dithiopir is within the range of from about 1: 2 to about 1:32. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its ester
    Petition 870180158325, of 12/04/2018, p. 10/36
    31/94 of benzyl or dithiopir. In one embodiment, the composition comprises the compound of Formula (I) and dithiopir, wherein the weight ratio of the compound of Formula (I) to dithiopir is about 1: 4 to about 1:32. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) or dithiopir, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to dithiopir is about 1: 2 to about 1 : 32. With respect to the methods, in certain modalities, the methods comprise contact of undesirable or local vegetation or application to soil or water to prevent the emergence or growth of vegetation by a composition described here. In some embodiments, the composition is applied at an application rate of from about 37 grams of active ingredient per hectare (g ai / ha) to about 2540 g ai / ha based on the total amount of active ingredients in the composition . In certain embodiments, the composition is applied at an application rate of from about 40 grams of active ingredient per hectare (g ai / ha) to about 200 g ai / ha based on the total amount of active ingredients in the composition . In some embodiments, the methods comprise contact of undesirable or local vegetation or application to soil or water to prevent the emergence or growth of vegetation with a compound of Formula (I) or salt or ester thereof and dithiopir or salt or ester of even, for example, sequentially or simultaneously. In some embodiments, dithiopir is applied at a rate of from about 35 g ai / ha to about 2240 g ai / ha and the compound of Formula (I) or salt or ester thereof is applied at a rate of from about 2 g ae / ha to about 300 g ae / ha. In some embodiments, dithiopir is applied at a rate of from about 17 g ai / ha to about 280 g ai / ha and the compound of Formula (I) or its salt or ester is applied at a rate of from about 2 g of acid equivalent per hectare (g ae / ha) to about 70 g ae / ha. And bad
    Petition 870180158325, of 12/04/2018, p. 37/109
    In some embodiments, dithiopir is applied at a rate of from about 35 g ai / ha to about 140 g ai / ha and the compound of Formula (I) or its salt or ester is applied in a rate from about 4.38 g of acid equivalent per hectare (g ae / ha) to about 3 g ae / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl ester and dithiopir. In one embodiment, the methods use the compound of Formula (I) and dithiopir, in which the compound of Formula (I) is applied at a rate of from about
    4.38 g of acid equivalent per hectare (g ae / ha) at about 35 g ae / ha and dithiopir is applied at a rate of about 35 g ai / ha to about 280 g ai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and dithiopir, in which the benzyl ester of the compound of Formula (I) is applied at a rate of from about 4.38 g of acid equivalent per hectare (g ae / ha) to about
    17.5 g ae / ha and dithiopir is applied at a rate of about 35 g ai / ha to about 140 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or salt or ester thereof in combination with dithiopir are used to control BRAPP, ECHCG, ECHCO, ECHOR, IPOHE, rSCPMA or XANST.
    [0048] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or salt or ester thereof is used in combination with oryzaline or salt thereof. With respect to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to oryzaline or salt thereof is within the range of from about 1: 3360 to about 1: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to oryzaline or salt thereof is within the range of about 1: 256 to about 1: 2. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to oryzaline or salt thereof is within the range from
    Petition 870180158325, of 12/04/2018, p. 38/109
    33/94 ca from 1:13 to about 1: 512. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to oryzaline or salt or ester thereof is within the range of from about 1:26 to about 1: 256. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl or oryzaline ester or salt thereof. In one embodiment, the composition comprises the compound of Formula (I) and oryzaline, wherein the weight ratio of the compound of Formula (I) to oryzaline is about 1:26 to about 1: 212. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and oryzaline, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to oryzaline is about 1:32 to about 1 : 256. With respect to the methods, in certain modalities, the methods comprise contact of the unwanted vegetation or local of the same or application to the soil or water to prevent the emergence or growth of vegetation by a composition described here. In some embodiments, the composition is applied at an application rate of from about 282 grams of active ingredient per hectare (g ai / ha) to about 7020 g ai / ha based on the total amount of active ingredients in the composition . In certain embodiments, the composition is applied at an application rate of from about 285 grams of active ingredient per hectare (g ai / h) to about 1150 g ae / ha based on the total amount of active ingredients in the composition . In some modalities, the methods comprise contact of the unwanted vegetation or local of the same or application to the soil or water to prevent the emergence or growth of vegetation with a compound of Formula (I) or salt or ester thereof and oryzaline or salt thereof, for example, sequentially or simultaneously. In some embodiments, oryzaline or salt or free base thereof is applied at a rate of from about 280 g ai / ha to about 6720 g ai / ha and the compound of Formula (I) or salt or
    Petition 870180158325, of 12/04/2018, p. 10/39
    34/94 ester of the same is applied at a rate of from about 2 g ae / ha to about 300 g ae / ha. In some embodiments, the salt of oryzaline is applied at a rate of from about 140 g ai / ha to about 2240 g ai / ha and the compound of Formula (I) or its salt or ester is applied at a rate of from about 2 g of acid equivalent per hectare (g ae / ha) to about 42 g ae / ha. In some embodiments, oryzaline or salt thereof is applied at a rate of from about 280 g ai / ha to about 1120 g ai / ha and the compound of Formula (I) or salt or ester thereof is applied at a rate from about 4.38 g of acid equivalent per hectare (g ae / ha) to about 32 g ae / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl and oryzaline ester. In one embodiment, the methods use the compound of Formula (I) and oryzaline, in which the compound of Formula (I) is applied at a rate of from about 5.3 g of acid equivalent per hectare (g ae / ha) at about 21.2 g ae / ha and oryzaline is applied at a rate of about 280 g ai / ha to about 1120 g ai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and oryzaline, in which the benzyl ester of the compound of Formula (I) is applied at a rate of from about 4.38 g to acid equivalent per hectare (g ae / ha) at about 17.5 g ae / ha and oryzaline is applied at a rate of about 280 g ai / ha to about 1120 g ai / ha. In certain embodiments, the methods and compositions using the compound of Formula (I) or salt or ester thereof in combination with oryzaline are used to control CYPDI, CYPES, CYPRO, ECHCG, IPOHE and SCPJU.
    [0049] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or salt or ester thereof is used in combination with pendimethalin or a salt thereof. With respect to the compositions, in some modalities, the weight ratio of the
    Petition 870180158325, of 12/04/2018, p. 10/40
    35/94 Formula (I) station or salt or ester thereof for pendimethalin or a salt thereof is within the range of from about 1: 1120 to about 1: 2. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to pendimethalin or a salt thereof is within the range of from about 1: 128 to about 1: 4. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to pendimethalin or a salt thereof is within the range of from about 1: 448 to about 1: 2. The rate of application will depend on the particular type of weed to be controlled, the degree of control required and the timing and method of application. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to pendimethalin or a salt thereof is within the range of from about 1: 4 to about 1: 250. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to pendimethalin or a salt thereof is within the range of from about 1: 8 to about 1: 128. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl or pendimethalyl ester. In one embodiment, the composition comprises the compound of Formula (I) and pendimethalin, wherein the weight ratio of the compound of Formula (I) to pendimethalin is about 1:16 to about 1: 128. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and pendimethalin, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to pendimethalin is about 1: 8 to about 1 : 128. With respect to methods, in certain modalities, the methods comprise contact of undesirable or local vegetation or application to soil or water to prevent the emergence or growth of vegetation by a composition described here. In some embodiments, the composition is applied at an application rate of from about 40 grams of
    Petition 870180158325, of 12/04/2018, p. 41/109
    36/94 active ingredient per hectare (g ai / ha) at about 1980 g ai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of from about 150 grams of active ingredient per hectare (g ai / ha) to about 600 g ai / ha based on the total amount of active ingredients in the composition . In certain embodiments, the composition is applied at an application rate of from about 150 grams of active ingredient per hectare (g ai / ha) to about 1190 g ai / ha based on the total amount of active ingredients in the composition . In some modalities, the methods comprise contact of the unwanted vegetation or local of the same or application to the soil or water to prevent the emergence or growth of vegetation with a compound of Formula (I) or salt or ester thereof and pendimethalin or a salt or base free of it, for example, sequentially or simultaneously. In some embodiments, pendimethalin or salt or free base thereof is applied at a rate of from about 140 g ai / ha to about 1680 g ai / ha and the compound of Formula (I) or salt or ester of it is applied at a rate of from about 2 g ae / ha to about 300 g ae / ha. In some embodiments, pendimethalin or a salt or free base thereof is applied at a rate of from about 70 g ai / ha to about 1120 g ai / ha and the compound of Formula (I) or salt or ester it is applied at a rate from about 2 g of acid equivalent per hectare (g ae / ha) to about 70 g ae / ha. In some embodiments, pendimethalin or a salt or free base thereof is applied at a rate of from about 140 g ai / ha to about 560 g ai / ha and the compound of Formula (I) or salt or ester of it is applied at a rate of from about 4.38 g of acid equivalent per hectare (g ae / ha) to about 35 g ae / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl ester or pendimethalin. In a modali
    Petition 870180158325, of 12/04/2018, p. 42/109
    37/94, the methods use the compound of Formula (I) and pendimethalin, in which the compound of Formula (I) is applied at a rate of from about 4.38 g of acid equivalent per hectare (g ae / ha) at about 35 g ae / ha and pendimethalin is applied at a rate of about 140 g ai / ha to about 560 g ai / ha. In one embodiment, the methods use the compound of Formula (I) and pendimethalin, where the compound of Formula (I) is applied at a rate of from about 2.5 g of acid equivalent per hectare (g ae / ha) at about 70 g ae / ha and pendimethalin is applied at a rate of about 140 g ai / ha to about 1120 g ai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and pendimethalin, in which the benzyl ester of the compound of Formula (I) is applied at a rate of from about 4.38g of acid equivalent per hectare (g ae / ha) to about 35 g ae / ha, and pendimethalin is applied at a rate of about 140 g ai / ha to about 560 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or salt or ester thereof in combination with pendimethalin or a salt thereof are used to control AMARE, BRNSW, CHEAL, CIRAR, CYPRO, DIGSA, ECHCG, ECHCO , IPOHE, KCHSC, LAMPU, LEFCH, PAPRH, SCPMA, SINAR or STEME.
    [0050] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or salt or ester thereof is used in combination with thiazopyr, salt, carboxylic acid, carboxylate salt or ester thereof. With respect to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to thiazopyr is within the range of from about 1: 1120 to about 6: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to thiazopyr is within the range of from about 1: 509 to about 1: 1. In certain embodiments, the compositions comprise the compound of Formula
    Petition 870180158325, of 12/04/2018, p. 43/109
    38/94 (I) or its benzyl and thiazopyr ester. With respect to the methods, in certain modalities, the methods comprise contact of the unwanted vegetation or local of the same or application to the soil or water to prevent the emergence or growth of vegetation by a composition described here. In some embodiments, the composition is applied at an application rate of from about 52 grams of active ingredient per hectare (g ai / ha) to about 2540 g ai / ha based on the total amount of active ingredients in the composition . In certain embodiments, the composition is applied at an application rate of from about 55 grams of active ingredient per hectare (g ai / ha) to about 1170 g ai / ha based on the total amount of active ingredients in the composition . In some embodiments, the methods comprise contact of unwanted or local vegetation or application to soil or water to prevent the emergence or growth of vegetation with a compound of Formula (I) or salt or ester thereof and thiazopyr, for example, sequentially or simultaneously. In some embodiments, thiazopyr is applied at a rate of from about 50 g ai / ha to about 2540 g ai / ha and the compound of Formula (I) of the salt or ester thereof is applied at a rate of from about 2 g ae / ha to about 300 g ae / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl ester and thiazopyr. In certain embodiments, methods and compositions using the compound of Formula (I) or salt or ester thereof in combination with thiazopyr or a salt thereof are used to control IPOHE or XANST.
    [0051] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or salt or ester thereof is used in combination with propizamide, salt, carboxylic acid, carboxylate salt or ester thereof. With respect to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or salt or
    Petition 870180158325, of 12/04/2018, p. 44/109
    39/94 ester of the same for tiazopir is within the range of from about 1: 600 to about 4: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or salt or ester thereof to propizamide is within the range of from about 1:35 to about 1: 2. In certain embodiments, the compositions comprise the compound of Formula (I) or its benzyl ester or propizamide. With respect to the methods, in certain modalities, the methods comprise contact of the unwanted vegetation or local of the same or application to the soil or water to prevent the emergence or growth of vegetation by a composition described here. In some embodiments, the composition is applied at an application rate of from about 72 grams of active ingredient per hectare (g ai / ha) to about 2500 g ai / ha based on the total amount of active ingredients in the composition . In certain embodiments, the composition is applied at an application rate of from about 78 grams of active ingredient per hectare (g ai / ha) to about 1152 g ai / ha based on the total amount of active ingredients in the composition . In some embodiments, the methods comprise contact of undesirable or local vegetation or application to soil or water to prevent the emergence or growth of vegetation with a compound of Formula (I) or salt or ester thereof and thiazopyr, for example, sequentially or simultaneously. In some embodiments, propizamide is applied at a rate of from about 70 g ai / ha to about 1200 g ai / ha and the compound of Formula (I) or its salt or ester is applied at a rate of from about 2 g ae / ha to about 300 g ae / ha. In some embodiments, propizamide is applied at a rate of from about 70 g ai / ha to about 1120 g ai / ha and the compound of Formula (I) or salt or ester thereof is applied at a rate of from about 2.5 g ae / ha to about 70 g ae / ha. In certain embodiments, the methods use the compound of Formula (I) or its ester of
    Petition 870180158325, of 12/04/2018, p. 10/45
    40/94 benzyl and propizamide. In certain embodiments, the methods and compositions using the compound of Formula (I) or salt or ester thereof in combination with propizamide or a salt thereof are used to control BRAPP, ECHCG, ECHCO, IPOHE, SEBEX or SETFA.
    [0052] The components of the mixtures described here can be applied either separately or as part of a multiple herbicide system.
    [0053] The mixtures described here can be applied in conjunction with one or more other herbicides to control a wider variety of unwanted vegetation. When used in conjunction with other herbicides, the composition can be formulated with another 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 here 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; 2.4DEP; 3,4-DP; 2,3,6-TBA; 2,4,5-T; 2,4,5-TB; acetochlor, acifluorfem, aclonifem, acrolein, alachlor, alidochlor, aloxidim, allyl alcohol, alorak, ametridione, amethrine, amibuzim, amicarbazone, amidosulfuron, aminocyclopyrachlor, aminopyralide, amiprofos-methyl, amylol, amitrol, amitrol, amitrol atratom, atrazine, azafenidim, azimsulfurom, aziprotrin, barbam, BCPC, beflubutamide, benazolim, bencarbazone, benfluralim, benfuresate, benssulfuron-methyl, bensulide, bentiocarb, bentazom-sodium, benzoform, benzobenzam, benzobenzam, benzam, benzam benztiazuron, bialafos, bicyclopyrone, bifenox, bilanafos, bispiribaque-sodium, borax, bromacila, bromobonil, bromobutide, bromophenoxim, bromoxonil, brompirazom, butachlor, butafenacil, butamachos, butenachlor, butenachlor
    Petition 870180158325, of 12/04/2018, p. 46/109
    41/94 dazol, butiuron, butralim, butroxidim, buturom, butylate, cacodyl acid, cafenstrol, calcium chlorate, calcium cyanamide, cambendichlor, carbasulam, carbetamide, carboxazol chlorprocarb, carfentrazone-ethyl, CDEA, CEPC, chloramethoxyene , clorazifope, chlorazin, clorbromurom, chlororbam, chloreturon, chlorfenac, chlorfenprope, chlorflurazol, chlorflurenol, chloridazone, chlorimurom, chlorornitrofem, chloropom, chlorotolurom, chloroxurom, chloroxynil, chlorprofam, cinnamon, chloride, chloride, chloride , cletodim, cliodinatio, clodinafope-propargila, clofope, clomazone, clomeprope, cloprope, cloproxidim, clopyralide, chloransulam-methyl, CMA, copper sulphate, CPMF, CPPC, credazine, cresol, cumiluron, cyanatrim, cyclamide, cyclamide, cyanoathinate, cyclamide, cyclamide, cyanathyrate, cyclamide, cyclone , cycloxidim, cyclurom, cyhalofop-butyl, cyperquate, cyprazine, cyprazole, cypromide, daimuron, dalapom, dazomete, delaclor, demedifam, demetrina, dialat dicamba, diclobenil, dichloralurea, dichlormate, diclorprope, dichlorprope-P, diclofope-methyl, diclosulam, dietamquate, diethyl, diphenopentem, diphenoxuron, difenzoquate, diflufenicam, diflufenzopim, dimfurimetam, dimefurimetam, dimefuramine, dinofenate, dinoprope, dinosam, dinosebe, dinoterb, diphenamide, dipropetrim, diquate, disuldiurom, DMPA, DNOC, DSMA, EBEP, eglinazine, endotal, epronaz, EPTC, erbom, esprocarb, etalfluralim, etbenzamide, etamenzamide, etamets, etamets etobenzamide, etofumesate, ethoxyfem, ethoxysulfuron, ethinofem, etnipromide, etobenzanide, EXD, fenasulam, fenoprope, phenoxaprope, phenoxaprope-P-ethyl, phenoxaprope-P-ethyl + isoxadifem-ethylal, phenoxysulfone, fentrazone, fentrazone, fentrazone , flamprope, flamprope-M, flazassulfurom, florasulam, fluazifope, fluazifop-P-butyl, fluazolate, flucarbazone, flucetosulfuron, flucloralim, flufenacete, flufenicam, flufenpir-ethyl , flumetsulam, flumezim, flumicloraque-pentila, flumioxazim, flumipropim, fluometurom, fluorodiphem, fluo
    Petition 870180158325, of 12/04/2018, p. 47/109
    42/94 roglicofem, fluormidina, fluornitrofem, fluotiurom, flupoxam, flupropacil, flupropanate, flupirsulfurom, fluridone, flurochloridone, fluroxypir, fluroxypyridate, flurtamone, flutiacet, fomesafem, glutofluoride, glutofluoride, glutamine, flushing , glufosinate-ammonium, glufosinate-P-ammonium, glyphosate, salts and esters of glyphosate, halauxifem, halauxifem-methyl, halosafem, halosulfurommethyl, haloxidine, haloxypop-methyl, haloxifop-P-methyl, hexachloramine, hexachloroacetone, hexachloramine , imazapic, imazapyr, imazaquim, imazosulfurom, imazetapyr, indanofam, indaziflam, iodobonyl, iodomethane, iodosulfurom, iodosulfuron-ethylsodic, iofensulfurom, ioxynil, ipazine, isfamimone, isopropyl, isopropyl, iodine , isoxabem, isoxaclortol, isoxaflutol, isoxapyrifope, carbutilate, cetospiradoxi, lactofem, lenacil, linurom, MAA, MAMA, ester ses and amines of MCPA, MCPA-thioethyl, MCPB, mecoprope, mecoprope-P, medinoterb, mefenacet, mefluidide, mesoprazine, mesosulfurom, mesotrione, metam, metamiprom metamitrom, metazachlor, metazosulfurom, metflurazom, metmeturimom, metallosmethyl, , metiuron, metometom, methoprotrin, methyl bromide, methyl isothiocyanate, metildimrom, metobenzurom, metobromurom, metolachlor, metosulam, methoxyurom, metribuzim, metsulfurom, metsulfurom-methyl, molinate, monalide, monalamide, mono MSMA, naproanilide, napropamide, naptalam, neburom, nicosulfuron, nipyraclofem, nitralim, nitrofem, nitrofluorfem, norflurazom, norurom, OCH, orbencarb, ortho-dichlorobenzene, orthosulfamurom, oxadiarmoxy, oxadomorphil, oxadiaromil, oxadiaromil, oxadiarmil, oxada paraflurom, paraquate, pebulate, pelargonic acidpenoxsulam, pentachlorophenol, pentanochlor, pentoxazom, perfluidone, petoxamide, phenisof am, fenmedifam, fenmedifam-ethyl, fenobenzurom,
    Petition 870180158325, of 12/04/2018, p. 48/109
    43/94 phenylmercury acetatp, picloram, picolinafem, pinoxadem, piperophos, potassium arsenite, potassium azide, potassium cyanate, pretilachlor, primisulfuromethyl, prociazine, prodiamine, profluazole, profluralim, propoxidimine, propoxidimine, propoxazione, propoxidimine, propoxidimine, propoxidimine, propoxidimine , prometrim, pronamide, propaclor, propanil, propaquizafope, propazine, profam, propisochlor, propoxycarbazone, propirisulfurom, prosulfalim, prosulfocarb, prosulfurom, proxam, prinachlor, pidanom, piraclonil, piraflufem-ethyl, pyrazoxyrazole, pyrazoxyrazole, pyrazoxazole , pyributicarb, pyriclor, pyridafol, pyridate, pyriftalide, pyriminobaque, pirimisulfam, piritiobaque-sodium, pyroxassulfone, pyroxsulam, quincloraque, quinmeraque, quinoclamine, quinonamide, quizalofope, quizalofope-P-ethyl, sulfacyl, rhodinacil, rhodinacil, rhodinacil, rhodinol, and , secbumetom, setoxidim, sidurom, simazine, simetom, simetrim, SMA, sodium arsenite, sodium azide, sodium chlorate, sulcotrione, sulfalate, sulfentrazone, sulfometuron, sulfosate, sulfosulfuron, sulfuric acid, sulglicapim, swep, SYN-523, TCA, tebutam, tebutiurom, tefuriltrione, tembotrione, tepraloxidim, terbacillin, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacil, terbacutan. , tetraflurom, tiazaflurontidiazimim, tidiazurom, tiencarbazone-methyl, tifensulfurom, tifensulfuron-methyl, thiobencarb, tiocarbazil, tioclorim, topramezone, tralcoxidim, triafamine, tri-tril, tromon, tromethamine, tromethamine, tromethamine, tromethamine, trilma esters and salts of triclopyr, tridifan, trietazine, trifloxysulfuron, trifluralim, triflussulfurom, trifope, trifopsima, trihydroxythriazine, trimeturon, tripropindam, tritosulfuron tritach, vernolate, xylachlor and the same isomers and esters.
    [0054] The compositions and methods described here can also be used in conjunction with glyphosate, 5enolpyruvylshiquime-3-phosphate (EPSP) synthase, glufosinate, glutamine synthetase inhibitors, dicamba, phenoxy auxins, pyridyloxy auxins, au
    Petition 870180158325, of 12/04/2018, p. 10/49
    44/94 synthetic xins, auxin transport inhibitors, aryloxyphenoxypropionates, cyclohexanediones, phenylpyrazolines, acetyl CoA carboxylase (ACCase) inhibitors, imidazolinones, sulfonylureas, pyrimidinylthiobenzoates, triazolpyrimidines, acetonylsulfonylsulfonylsulfonylsulfonates (AHAS), 4-hydroxyphenyl-pyruvate dioxigenase (HPPD) inhibitors, phytoene desaturase inhibitors, carotenoid biosynthesis inhibitors, protoporphyrinogen oxidase (PPO) inhibitors, cellulose biosynthesis inhibitors, mitosis inhibitors, microtubule inhibitors, of very long chain fatty acid, inhibitors of fatty acid and lipid biosynthesis, photosystem inhibitors I, photosystem inhibitors II, triazines and bromoxynil in glyphosate tolerant cultures, tolerant to EPSP synthase inhibitor, tolerant to glufosinate, tolerant to inhibitor glutamine synthetase, dicamba tolerant, to phenoxy auxin readers, tolerant to pyridyloxy auxin, auxin tolerant, tolerant to auxin transport inhibitor, tolerant to aryloxyphenoxypropionate, tolerant to cyclohexanedione, tolerant to phenylpyrazoline, tolerant to ACCase, tolerant to imidazolinone, tolerant to sulfonylurea, tolerant to sulfonylurea pyrimidinylthiobenzoate, tolerant to triazolpyrimidine, tolerant to sulfonylaminocarbonyltriazolinone, tolerant to ALS or AHAS, tolerant to HPPD, tolerant to phytene inhibitor desaturase, tolerant to carotenoid biosynthesis inhibitor, tolerant to PPO inhibitors, tolerant to cellulose inhibitor tolerants mitosis, tolerant to microtubule inhibitor, tolerant to very long chain fatty acid inhibitor, tolerant to fatty acid and lipid biosynthesis inhibitor, tolerant to photosystem I inhibitor, tolerant to photosystem II inhibitor, tolerant to triazine, tolerant to bromoxynil and cultures having ca Multiple or stacked features giving tolerance to multiple chemicals and / or multiple modes of action via single or multiple resistance mechanisms. And bad
    Petition 870180158325, of 12/04/2018, p. 50/109
    45/94 In some modalities, the compound of Formula (I) or salt or ester of the same and herbicide or salt or ester of the same complement are used in combination with herbicides that are selective for the culture being treated and that complement the spectrum of herbs- weeds controlled by these compounds at the application rate employed. In some embodiments, the compositions described here and other complementary herbicides are applied at the same time, either as a combination formulation, as a tank mix or as a sequential application.
    [0055] In some embodiments, the compositions described here are used in combination with one or more herbicide protectors, such as AD-67 (MON 4660), benoxacor, bentiocarb, brassinolide, cloquintocete (mexila), ciometrinila, daimurom, diclormida, dicyclonone, dimepiperate, disulfoton, fenclorazol-ethyl, fenclorin, flurazole, fluxofenim, furilazol, hairpin proteins, isoxadifene-ethyl, jiecaowan, jiecaoxi, mefenpir-diethyl, mefenate, naphthenic acid, and amine oxide; of N-phenylsulfonylbenzoic acid, to increase its selectivity. In some modalities, protectors are used in rice, cereal or corn environments. In some embodiments, the protector is cloquintocet or an ester or salt thereof. In certain embodiments, cloquintocet is used to antagonize harmful effects of the compositions on rice and cereals. In some modalities, the protector is cloquintocete (mexila).
    [0056] In some embodiments, the compositions described here are used in combination with one or more plant growth regulators, such as 2,3,5-triiodiodobenzoic acid, IAA, IBA, naphthaleneacetamide, α-naphthaleneacetic acids, benzyladenine , alcohol 4-hydroxyphenethyl, quinetin, zeatin, endotal, etefom, pentachlorophenol, thiadiazuron, tribufos, aviglycine, gibberellins, gibberellic acid, abscisic acid, ancimidol, phosamine, glyphosine, isopyrimol, jas acid
    Petition 870180158325, of 12/04/2018, p. 51/109
    46/94 mononic, maleic hydrazide, mepiquate, 2,3,5-triiodiodobenzoic acid, morphactins, dichlorflurenol, flurprimidol, mefluidide, paclobutrazol, tetciclacis, uniconazole, brassinolide, brassinolide-ethyl, cyclohexamide oxide, ethylene oxide , triapentenol and trinexapaque.
    [0057] 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, cane sugar, sunflower, grassland, grassland, pasture, fallow, grass, tree and vine orchards, plantation crops, vegetables and non-culture (ornamental) environments. In some embodiments, the plant growth regulator is mixed with the compound of Formula (I) or mixed with the compound of Formula (I) and microtubule inhibiting herbicides to cause a preferentially beneficial effect on plants.
    [0058] In some embodiments, the compositions provided here further comprise at least one agriculturally acceptable adjuvant or carrier. Adequate adjuvants or carriers should not be phytotoxic to valuable crops, particularly at concentrations used in applying selective weed control compositions in the presence of crops and should not react chemically with herbicidal components or other ingredients in the composition. Such 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 carriers and adjuvants before application. They can be solid, such as, for example, fine powders, granules, water-dispersible granules or wetting powders, or liquids such as, for example, emulsifiable concentrates, solutions, emulsions or suspensions. They can also be provided as a premix or mixed in a tank.
    [0059] Suitable agricultural adjuvants and carriers include,
    Petition 870180158325, of 12/04/2018, p. 52/109
    47/94 but are not limited to, culture oil concentrate; nonylphenol ethoxylate; benzylcocoalkylimethyl quaternary ammonium salt, mixture of petroleum hydrocarbonate, alkyl esters, organic acid and anionic surfactant; C9-C11 alkyl polyglycoside, phosphate alcohol ethoxylate; primary alcohol (C12-C16) ethoxylate; block copolymer of di-sec-butylphenol EP-PO; polysiloxane-methyl cap; nonylphenol ethoxylate + urea ammonium nitrate; emulsified methylated seed oil; tridecyl alcohol ethoxylate (synthetic) (8 EO); tallow amine ethoxylate (15 EO); PEG (400) dioleate-99.
    [0060] The liquid carriers that can be used include water and organic solvents. Organic solvents include, but are not limited to, petroleum or hydrocarbon fractions such as mineral oil, aromatic solvents, paraffinic oils and the like; vegetable oils such as soybean oil, rapeseed oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cottonseed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, tung oil and the like; esters of the above vegetable oils; esters of monoalcohols or dihydric, trihydric or lower polyalcohols (containing 4-6 hydroxy), such as 2-ethyl hexyl stearate, n-butyl oleate, isopropyl myristate, propylene glycol dioleate, di-octyl succinate, adipate di-butyl, di-octyl phthalate and the like; esters of mono-, di- and polycarboxylic acids and the like. Specific organic solvents include, but are not limited to, toluene, xylene, petroleum naphtha, culture oil, acetone, methyl ethyl ketone, cyclohexanone, trichlorethylene, perchlorethylene, ethyl acetate, amyl acetate, butyl acetate, propylene glycol monomethyl ether and diethylene glycol monomethyl ether, methyl alcohol, ethyl alcohol, isopropyl alcohol, amyl alcohol, ethylene glycol, propylene glycol, glycerin, N-methyl-2-pyrrolidionone, N, Ndimethyl alkylamides, dimethyl sulfoxide, liquid fertilizers and simi
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    48/94 home. In certain modalities, water is the carrier for the dilution of concentrates.
    [0061] Suitable solid carriers include, but are not limited to, talc, pyrophyllite clay, silica, atalpulgite clay, kaolin clay, kieselguhr, chalk, diatomaceous earth, lime, calcium carbonate, bentonite clay, Fuller earth, seed husks cotton, wheat flour, soy flour, pumic, sawdust, nutshell flour, lignin, cellulose and the like.
    [0062] In some embodiments, the compositions described here further comprise one or more surfactants. In some modalities, such surfactants are used in both solid and liquid compositions and in certain modalities those designed to be diluted with carrier before application. Surfactants can be anionic, cationic or non-ionic in 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, inter alia, in [0063] 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 diethanol-ammonium lauryl sulfate; alkylarylsulfonate salts, such as calcium dodecylbenzenesulfonate; alkylphenol-alkylene oxide addition products, such as C18 nonylphenol ethoxylate; alcohol-alkylene oxide addition products, such as tridecyl C6-alcohol ethoxylate; soaps, such as sodium stearate; alkylnaphthalene sulfonate salts, such as sodium dibutylnaphthalenesulfonate; dialkyl esters of sulfosuccinate salts, such as sodium di (2-ethylhexyl) sulfosuccinate; sorbitol esters, such as oleate of
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    49/94 sorbitol; quaternary amines, such as lauryl trimethylammonium chloride; polyethylene glycol 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 oil, coconut oil, corn oil, cottonseed oil, linseed oil, palm oil , peanut oil, safflower oil, sesame oil, tung oil and the like; and esters of the above vegetable oils, and in certain embodiments, methyl esters.
    [0064] In some embodiments, these materials, such as vegetable and seed oils and their esters, can be used interchangeably as an agricultural adjuvant, as a liquid carrier or as a surfactant.
    [0065] Other exemplary additives for use in the compositions provided herein include, but are not limited to, compatibilizing agents, antifoaming agents, sequestering agents, neutralizing agents and buffers, corrosion inhibitors, dyes, odorants, spreading agents, auxiliaries penetration agents, tackifiers, dispersing agents, thickening agents, freezing point depressants, antimicrobial agents and the like. The compositions can also contain other compatible components, for example, other herbicides, plant growth regulators, fungicides, insecticides and the like and can be formulated with liquid or solid fertilizers, particulate fertilizer carriers such as ammonium nitrate, urea and the like.
    [0066] In some embodiments, the concentration of the active ingredients in the compositions described here is from about 0.0005 to 98 weight percent. In some embodiments, the concentration is from about 0.0006 to 90 weight percent. In composition
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    50/94 tions designed to be used as concentrates, the active ingredients, in certain modalities, are present in a concentration of from about 0.1 to 98 weight percent and in certain modalities about 0.5 to 90 percent by weight. Such compositions are, in certain embodiments, diluted with an inert carrier, such as water, before application. The diluted compositions generally applied to weeds or to the location of weeds contain, in certain embodiments, about 0.0006 to 10.0 weight percent of active ingredient and in certain embodiments contain about 0.001 to 6.0 percent by weight.
    [0067] The present compositions can be applied to weeds or their location through the use of ground or aerial sprinklers, sprayers and granule applicators, through addition to irrigation water or rice fields and through other conventional means known to those skilled in the art .
    [0068] The modalities described and the examples that follow 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 here will be apparent to a common person skilled in the art without departing from the spirit and scope of the claimed object matter.
    Examples [0069] Results in Examples I, II, III and IV are greenhouse test results.
    Example I. Evaluation of Herbicidal Mixtures Applied to Post-emergence Leaf for Weed Control in Direct Seeded Rice [0070] Seeds or small nuts of the desired test plant species were planted in a soil matrix prepared by mixing clayey soil or sandy loam (for example, 28.6 per
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    51/94 percent sediment and 52.6 percent sand, with a pH of about 5.8 and an organic matter content of about 1.8 weight percent) and limestone sand in an 80 to 20 ratio The soil matrix was contained in plastic pots with a volume of 1 quarter and a surface area of 83.6 cm 2 . When necessary to ensure good germination and healthy plants, a fungicide 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 hours that was maintained at about 29 ° C during the day and 26 ° C at night. The nutrients (Peters Excel® 15-5-15 5-Ca 2-Mg and iron chelate) were applied to the irrigation solution as needed and water was added on a regular basis. Supplementary lighting was provided with 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.
    [0071] The treatments consisted of the amino acid or esters of 4 amino-3- chloro-5- fluorine-6- (4-chloro-2-fluoro-3-methoxy-phenyl) pyridine-2-carboxylic acid (Compound A), each formulated as a SC (suspension concentrate) and various herbicidal components alone and in combination. Compound A forms were applied on an acid equivalent basis.
    [0072] Forms of compound A (compound of Formula I) tested include:
    Acid Compound
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    ch 3
    Compound B n-Butyl ester
    Benzyl Ester Compound [0073] Other herbicidal components were applied on an active ingredient basis and included microtubule inhibiting herbicides (MTI) pendimethalin applied as Prowl® 3.3EC, dithiopir applied as Dithiopyr WP, oryzaline applied as Surflan® SC, propizamide formulated as Kerb® 50WP, thiazopyr (technical grade material).
    [0074] Treatment needs 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.
    [0075] For treatments comprised of formulated compounds, measured amounts of compounds were individually placed in 25 ml glass bottles and diluted in a volume of 1.25% (v / v) of Agri-Dex® culture oil concentrate for get 12X stock solutions. If a test compound did not readily dissolve, the mixture was heated and / or sonicated.
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    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 a 1.25% (v / v) aqueous mixture of concentrate of culture oil so that the final spray solutions contained 1.25 + / 0.05% (v / v) of culture oil concentrate.
    [0076] For treatments comprised of technical compounds, the weighed quantities can be placed individually in 25 ml glass bottles and dissolved in a volume of 97: 3 v / v acetone / DMSO to obtain 12X stock solutions. If a test compound does not readily dissolve, the mixture can 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 a 1.5% (v / v) aqueous mixture of culture oil concentrate so that the final spray solutions contain 1.25% (v / v) culture oil concentrate. When technical materials are used, concentrated stock solutions can be added to the spray solutions so that the final concentrations of acetone and DMSO in the application solutions are 16.2% and 0.5%, respectively.
    [0077] For treatments comprised of formulated and technical compounds, heavy amounts of the technical materials were individually placed in 25 mL glass vials and dissolved in a 97: 3 v / v volume of acetone / DMSO to obtain 12X and Measured amounts of the formulated compounds were individually placed in 25 ml glass bottles and diluted in a volume of 1.5% (w / w) of culture oil or water concentrate to obtain 12x stock solutions. If a test compound is not
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    54/94 dissolved readily, the mixture was heated and / or sonicated. 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 a 1.5% (v / v) of culture oil concentrates so that the final spray solutions contained 1.25% (v / v) of culture oil concentrate. As needed, additional water and / or 97: 3 v / v acetone / DMSO was added to individual application solutions so that the final acetone and DMSO concentrations of the application solutions being compared were 8.1% and 0.25 %, respectively.
    [0078] All stock solutions and application solutions were visually inspected for compound compatibility prior to application. Spray solutions were applied to the plant material with a suspended Mandel strip sprayer equipped with 8002E nozzles calibrated to apply 187 J / ha in an application area of 0.503 m 2 at a spray height of 46 to 50 cm (18 to 20 inches) above the canopy height of the average plant. Control plants were sprayed in the same way with the solvent without activity.
    [0079] The treated plants and the control plants were placed in a greenhouse as described above and wetted by sub-irrigation to prevent run-off of the test compounds. After approximately 3 weeks, the condition of the test plants compared to that of the 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 .
    [0080] Colby's equation was used to determine the effects
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    55/94 herbicides expected from the mixtures (Colby, S.R. 1967. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 15: 20-22).
    [0081] 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 in the same concentration as used in the mixture.
    B = observed effectiveness of active ingredient B at the same concentration as used in the mixture.
    The compounds tested, rates of application employed, plant species tested and results are given in Tables 1-10.
    Table 1. Synergistic Activity of Acid Compound and
    Herbicidal Compositions of Pendimethalin Applied to Leaf on Weed Control in a Rice Culture System.
    Compound AAcid Pendimethalin Visual Weed Control (%) - 19 DAA DIGSA g ae / ha g ai / ha Note Exp 4.38 0 30 - 0 140 0 - 0 280 0 - 4.38 140 50 30 4.38 280 45 30
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    Compound AAcid Pendimethalin Visual Weed Control (%) - 19 DAA ECHCG g ae / ha g ai / ha Note Exp 4.38 0 60 - 0 140 0 - 0 280 0 - 0 560 10 - 4.38 140 80 60 4.38 280 85 60 4.38 560 95 64
    Acid Compound Pendimethalin Visual Weed Control (%)- 19 DAA IPOHE g ae / ha g ai / ha Note Exp 4.38 0 0 - 8.75 0 10 - 0 140 0 - 0 280 0 - 0 560 0 - 4.38 140 15 0 8.75 140 15 10 4.38 280 20 0 8.75 280 25 10
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    Acid Compound Pendimethalin Visual Weed Control (%)- 19 DAA 4.38 560 15 0 8.75 560 20 10
    Compound AAcid Pendimethalin Visual Weed Control (%) - 21 DAA IPOHE g ae / ha g ai / ha Note Exp 35 0 45 - 0 1120 13 - 35 1120 70 52
    Table 2. Synergistic Activity of Benzyl Ester Compound and Herbicidal Compositions of Pendimethalin Applied to Leaf on Weed Control in a Rice Culture System.
    Benzyl Ester Compound Pendimethalin Visual Weed Control(%) - 19 DAA DIGSAg ae / ha g ai / ha Note Exp 4.38 0 35 - 8.75 0 50 - 0 140 0 - 0 280 0 - 4.38 140 45 35 8.75 140 50 50
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    Benzyl Ester Compound Pendimethalin Visual Weed Control(%) - 19 DAA 4.38 280 50 35 8.75 280 70 50
    Compound AEster ofBenzila Alina pendimet Visual Weed Control (%) - 19DAA ECHCG ECHCO IPOHE g ae / ha g ai / ha Note Exp Note Exp Note Exp 4.38 0 55 - 65 - 0 - 8.75 0 85 - 90 - 0 - 0 140 0 - 0 - 0 - 0 280 0 - 0 - 0 - 0 560 10 - 0 - 0 - 4.38 140 75 55 85 65 25 0 8.75 140 90 85 95 90 10 0 4.38 280 85 55 90 65 15 0 8.75 280 95 85 95 90 25 0 4.38 560 90 60 90 65 10 0 8.75 560 95 87 95 90 15 0
    Benzyl Ester Compound Pendimethalin Visual Weed Control(%) - 19 DAA LEFCH g ae / ha g ai / ha Note Exp
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    Benzyl Ester Compound Pendimethalin Visual Weed Control(%) - 19 DAA 4.38 0 0 - 8.75 0 25 - 17.5 0 30 - 0 140 0 - 0 280 20 - 0 560 80 - 4.38 140 20 0 8.75 140 40 25 17.5 140 50 30 4.38 280 45 20 8.75 280 65 40 17.5 280 85 44 4.38 560 85 80 8.75 560 90 85 17.5 560 99 86
    Table 3. Synergistic Activity of n-Butyl Ester Compound and Herbicidal Compositions of Pendimethalin Applied to Leaf under Weed Control in a Rice Culture System.
    N-Butyl Ester Compound Pendimethalin Visual Weed Control(%) - 21 DAA ECHCG g ae / ha g ai / ha Note Exp 17.5 0 45 -
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    N-Butyl Ester Compound Pendimethalin Visual Weed Control(%) - 21 DAA ECHCG g ae / ha g ai / ha Note Exp 35 0 70 - 0 1120 18 - 17.5 1120 90 55 35 1120 99 75
    Compound AN- esterButila Pendimethalin Visual Weed Control (%) -21 DAA IPOHEg ae / ha g ai / ha Note Exp 17.5 0 40 - 0 1120 13 - 17.5 1120 63 48
    Table 4. Synergistic Activity of Acid Compound and Herbicidal Compositions of Dithiopir Applied to Leaf on Weed Control Common to Rice Culture Systems.
    Acid Compound Dithiopir Visual Weed Control(%) -21 DAA BRAPP g ae / ha g ai / ha Note Exp 8.75 0 60 - 0 35 0 -
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    Acid Compound Dithiopir Visual Weed Control(%) -21 DAA 0 70 0 - 0 140 0 - 8.75 35 90 60 8.75 70 75 60 8.75 140 90 60
    Acid Compound Dithiopir Visual Weed Control (%) -21 DAA ECHCO g ae / ha g ai / ha Note Exp 4.38 0 60 - 8.75 0 90 - 0 35 0 - 0 70 0 - 0 140 0 - 4.38 35 90 60 8.75 35 95 90 4.38 70 95 60 8.75 70 95 90 4.38 140 95 60 8.75 140 95 90
    Table 5. Synthetic Activity of Benzyl Ester Compound and Herbicidal Compositions of Dithiopir Applied to Leaf on Control of
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    Weeds Common to Rice Culture Systems.
    Ester CompoundBenzila Dithiopir Visual Weed Control (%)- 21 DAA BRAPP g ae / ha g ai / ha Note Exp 4.38 0 70 - 0 35 0 - 0 70 0 - 0 140 0 - 4.38 35 75 70 4.38 70 85 70 4.38 140 85 70
    Benzyl Ester Compound Dithiopir Visual Weed Control (%)- 21 DAA IPOHE g ae / ha g ai / ha Note Exp 4.38 0 10 - 8.75 0 10 - 17.5 0 25 - 0 35 10 - 4.38 35 20 19 8.75 35 35 19 17.5 35 45 33
    Table 6. Synergistic Activity of Acid Compound and Compositions
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    Orizaline Herbicides Applied to Leaf on Common Weed Control in Rice Culture Systems.
    Acid Compound Orizalina Visual Weed Control (%)- 20 DAA CYPES g ae / ha g ai / ha Note Exp 5.3 0 0 - 10.6 0 90 - 0 280 0 - 0 560 0 - 0 1120 0 - 5.3 280 75 0 10.6 280 95 90 5.3 560 20 0 10.6 560 100 90 5.3 1120 50 0 10.6 1120 100 90
    Acid Compound Orizalina Visual Weed Control (%) - 20 DAA CYPDI SCPJU g ae / ha g ai / ha Note Exp Note Exp 5.3 0 80 - 25 - 0 280 0 - 0 - 0 560 0 - 0 -
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    CompoundThe Acid Orizalina Visual Weed Control (%) - 20 DAA CYPDI SCPJU g ae / ha g ai / ha Note Exp Note Exp 0 1120 0 - 0 - 5.3 280 90 80 95 25 5.3 560 95 80 99 25 5.3 1120 95 80 99 25 Table 7. Al Synergistic activity of Compound A Benzyl and Ester Compound
    Herbicide positions of Orizalina Applied to Leaf on Weed Control Common to Rice Culture Systems.
    Benzyl Ester Compound Orizalina Visual Weed Control (%) -20 DAA ECHCG g ae / ha g ai / ha Note Exp 4.38 0 40 - 8.75 0 70 - 0 280 0 - 0 560 10 - 0 1120 15 - 4.38 280 55 40 8.75 280 75 70 4.38 560 65 46 8.75 560 85 73 4.38 1120 65 49 8.75 1120 80 75
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    Benzyl Ester Compound Orizalina Visual Weed Control (%)- 20 DAA IPOHE g ae / ha g ai / ha Note Exp 8.75 0 10 - 17.5 0 25 - 0 1120 15 - 8.75 1120 40 24 17.5 1120 50 36
    Table 8. Synergistic Activity of Acid Compound and Herbicidal Compositions of Propizamide Applied to Leaf on Control of Weeds Common to Rice Culture Systems.
    Acid Compound Propamide Visual Weed Control (%) -22 DAA IPOHE g ae / ha g ai / ha Note Exp 8 0 25 - 16 0 35 - 32 0 40 - 0 70 0 - 0 140 0 - 0 280 0 - 8 70 NT 25 16 70 70 35 32 70 60 40
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    Acid Compound Propamide Visual Weed Control (%) -22 DAA IPOHE g ae / ha g ai / ha Note Exp 8 140 60 25 16 140 60 35 32 140 65 40 8 280 30 25 16 280 35 35 32 280 65 40
    Table 9. Synergistic Activity of Benzyl Ester Compound and Herbicidal Compositions of Propizamide Applied to Leaf on Weed Control Common to Rice Culture Systems.
    Benzyl Ester Compound Propamide Visual Weed Control (%) - 22 DAA IPOHE g ae / ha g ai / ha Note Exp 8 0 10 - 16 0 10 - 32 0 35 - 0 70 0 - 0 140 0 - 0 280 0 - 8 70 20 10 16 70 20 10 32 70 50 35
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    Benzyl Ester Compound Propamide Visual Weed Control (%) - 22 DAA 8 140 20 10 16 140 20 10 32 140 50 35 8 280 10 10 16 280 50 10 32 280 85 35
    Table 10. Synergistic Activity of Benzyl Ester Compound Applied to Leaf and Herbicidal Compositions of Tiazopir Applied to Leaf on Weed Control Common to Rice Culture Systems.
    Benzyl Ester Compound Tiazopir Visual Weed Control (%) - 20 DAA IPOHE g ae / ha g ai / ha Note Exp 8 0 20 - 16 0 40 - 0 280 40 - 8 280 75 52 16 280 70 64
    BRAPP Brachiaria platyphylla (Griseb.) Nash brachiaria CYPES Cyperus esculentus L. broad sheet (signalgrass,broadleaf)yellow nutsedge (nutsed- CYPDI Cyperus difformis L. ge, yellow) scaup
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    68/94 smallflower umbrella)
    DIGSA Digitaria sanguinalis (L.) Scop. Grass mattress grass, large) (Crab- ECHCG Echinochloa crusgalli (L.) Beauv. Rice grass (Pub- nyardgrass)ECHCO Echinochloa colona (L.) Link colony grass (together glerice)IPOHE Ipomoea hederacea Jacq. jeticuçu (morningglory, ivyleaf)LEFCH Leptochloa chinensis (L.) Nees spring top Chinese (sprangletop,
    Chinese)
    SCPJU Schoenoplectus juncoides (Roxb.) Palla junco Japanese (bulrush, Japanese)
    NT = Not tested g ae / ha = grams of acid equivalent per hectare g ai / ha = grams of active ingredient per hectare
    Obs = observed value
    Exp = expected value as calculated using the Colby DAA equation = days after application
    Example II. Evaluation of Herbicidal Mixtures Applied in Water for Weed Control in Transplanted Rice Fields [0082] The small weed seeds or nuts of the desired test plant species were planted in drenched soil (mud) prepared by mixing a non-sterilized mineral soil , chopped (50.5 percent sediment, 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 in a 1: 1 volumetric ratio. The prepared sludge was applied in 365 mL aliquots in unperforated (16 oz - oz) plastic pots with a surface area of
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    86.59 square centimeters (cm 2 ) leaving an upper free 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 30 percent, in plastic buffer trays. The seedlings in the second or third growth stage were transplanted to 860 mL of mud contained in unperforated (32 oz) plastic pots with a surface area of 86.59 cm 2 for 4 days before applying the herbicide. The rice paddy was created by filling the top free space of the pots with 2.5 to 3 cm of water. When necessary to ensure plants with good germination and healthy, a treatment with fungicide and / or other chemical or physical or applied treatment. The plants were grown for 4-22 days in a greenhouse with an approximate 14-hour photoperiod that was maintained at around 29 ° C during the day and 26 ° C at night. The nutrients were added as Osmocote® (19: 6: 12, N: P: K = nutrients in smaller quantities) in 2 g per (480 ml (16 oz.) Pot and 4 g per 946 ml (32 oz. Pot) .)). Water was added on a regular basis to keep the rice paddy flooded and supplemental light was provided with 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.
    [0083] 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 various herbicidal components alone or in combination. Compound A forms were applied on an acid equivalent basis. The forms of compound A (compound of Formula I) tested included:
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    Acid Compound

    ch 3
    N-Butyl Ester Compound
    Benzyl Ester Compound [0084] Other herbicidal components were applied on an active ingredient basis and included microtubule inhibiting herbicides (MTI) (Microtubule Inhibiting) pendimethalin applied as Prowl® 3.3EC, dithiopir applied as Dithiopir WG and oryzaline applied as Surflan® SC.
    [0085] The treatment needs for each herbicide compound or component were calculated based on the rates being tested, the concentration of active ingredient or acid equivalent in
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    71/94 formulation, an application volume of 2 mL per component per pot and an application area of 86.59 cm 2 per pot.
    [0086] 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) of Agri-Dex® culture oil concentrate for obtain application solutions. If the test compound does not dissolve quickly, the mixture was heated and / or sonicated. [0087] For technical grade compounds, a heavy amount was placed in an individual glass bottle of 100 to 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 obtained were diluted with an equivalent volume of an aqueous mixture containing 2.5% (v / v) of culture oil concentrate so that the final application solutions contained 1.25% (v / v) of culture oil concentrate.
    [0088] The applications were made through injection, with a pipette, of appropriate amounts of the application solutions in the aqueous layer of the rice field. Control plants were treated in the same way with the solvent without activity. The applications were made in such a way that all the treated plant material received the same concentrations of acetone and culture oil concentrate.
    [0089] The treated plants and the control plants were placed in a greenhouse as described above and water was added as needed to maintain a flooded rice field. After approximately 3 weeks the condition of the test plants compared to those of the 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.
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    72/94 [0090] 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).
    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 in the same concentration as used in the mixture.
    B = observed effectiveness of active ingredient B at the same concentration as used in the mixture.
    [0091] The tested compounds, application rates employed, tested plant species and results are given in Tables 1117.
    Table 11. Synergistic activity of Water Applications of Acid Compound and Herbicidal Compositions of Pendimethalin on Weed Control in a Rice Culture System.
    Acid Compound Pendimethalin Visual Weed Control(%) - 21 DAA ECHCGg ae / ha g ai / ha Note Exp 8.75 0 0 - 17.5 0 0 - 35 0 20 - 0 280 20 - 0 560 0 - 8.75 280 10 20
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    Acid Compound Pendimethalin Visual Weed Control(%) - 21 DAA ECHCG g ae / ha g ai / ha Note Exp 17.5 280 60 20 35 280 60 36 8.75 560 55 0 17.5 560 100 0 35 560 40 20
    Compound AAcid Pendimethalin Visual Weed Control(%) - 21 DAA LEFCH g ae / ha g ai / ha Note Exp 8.75 0 0 - 17.5 0 0 - 35 0 30 - 0 280 40 - 8.75 280 50 40 17.5 280 100 40 35 280 100 58
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    Table 12. Synergistic Activity in Water Applications of Benzyl Ester Compound and Herbicidal Compositions of Pendimethalin on Weed Control in a Rice Culture System.
    Benzyl Ester Compound Pendimethalin Visual Weed Control(%) - 21 DAA ECHCG g ae / ha g ai / ha Note Exp 4.38 0 0 - 8.75 0 0 - 17.5 0 25 - 0 280 20 - 0 560 0 - 4.38 280 40 20 8.75 280 35 20 17.5 280 30 40 4.38 560 95 0 8.75 560 50 0 17.5 560 95 25
    Benzyl Ester Compound Pendimethalin Control of(%) - 21 DAA Visual Weed CYPRO g ae / ha g ai / ha NoteExp 8.75 0 0- 17.5 0 0-
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    Benzyl Ester Compound Pendimethalin Visual Weed Control(%) - 21 DAA CYPRO g ae / ha g ai / ha Note Exp 0 280 0 - 0 560 0 - 8.75 280 20 0 17.5 280 20 0 8.75 560 40 0 17.5 560 50 0
    Benzyl Ester Compound Pendimethalin Visual Weed Control (%) -21 DAA SCPMA g ae / ha g ai / ha Note Exp 4.38 0 0 - 8.75 0 0 - 17.5 0 0 - 0 560 0 - 4.38 560 95 0 8.75 560 40 0 17.5 560 50 0
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    Benzyl Ester Compound Pendimethalin Visual Weed Control(%) - 21 DAA LEFCH g ae / ha g ai / ha Note Exp 35 0 50 - 70 0 50 - 0 1120 48 - 35 1120 78 74 70 1120 92 74
    Table 13. Synergistic Activity of n-Butyl Ester Compound Water Applications and Pendimethalin Herbicidal Compositions on Weed Control in a Rice Culture System.
    Compound AN- esterButila Pendimethalin Visual Weed Control(%) - 21 DAA LEFCH g ae / ha g ai / ha Note Exp 35 0 8 - 70 0 38 - 0 1120 48 - 35 1120 65 51 70 1120 78 67
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    Table 14. Synergistic Activity of Applications in Acid Compound Water and Herbicidal Compositions of Dithiopir on Control of Weeds Common to Rice Culture Systems.
    Acid Compound Dithiopir Visual Weed Control (%) -21 DAA ECHOR SCPMA g ae / ha g ai / ha Note Exp Note Exp 8.75 0 10 - 0 - 17.5 0 40 - 0 - 35 0 40 - 0 - 0 70 30 - 0 - 8.75 70 40 37 50 0 17.5 70 100 58 100 0 35 70 100 58 100 0
    Table 15. Synergistic Activity of Water Applications of Benzyl Ester Compound and Herbicidal Compositions of Dithiopir on Weed Control Common to Rice Culture Systems.
    Ester Compound Dithiopir Control of Weed Vi- Benzila sual (%) - 21 DAA ECHOR g ae / ha g ai / ha Note Exp 4.38 0 40 - 8.75 0 60 - 17.5 0 75 - 0 70 30 -
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    Ester Compound Dithiopir Control of Weed Vi- Benzila sual (%) - 21 DAA ECHOR g ae / ha g ai / ha Note Exp 4.38 70 90 58 8.75 70 70 72 17.5 70 99 83
    Table 16. Synergistic Activity of Water Applications of Acid Compound and Herbicidal Compositions of Orizalina on Weed Control Common to Rice Culture Systems.
    Compound AAcid Orizalina Visual Weed Control (%) -20 DAA CYPRO g ae / ha g ai / ha Note Exp 10.6 0 10 - 21.2 0 20 - 0 560 0 - 0 1120 0 - 10.6 560 50 10 21.2 560 50 20 10.6 1120 50 10 21.2 1120 90 20
    Table 17. Synergistic Activity of Water Applications of Benzyl Ester Compound and Oryzaline Herbicidal Compositions on Weed Control Common to Rice Culture Systems.
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    Ester CompoundBenzila Orizalina Visual Weed Control (%) - 20 DAA CYPRO g ae / ha g ai / ha Note Exp 4.38 0 50 - 8.75 0 0 - 17.5 0 90 - 0 560 0 - 4.38 560 80 50 8.75 560 85 0 17.5 560 90 90
    CYPRO
    Cyperus rotundus L.
    ECHCG
    ECHOR
    Echinochloa crus-galli (L.) Beauv.
    Echinochloa oryzoides (Ard.) Fritsch tiririca purpura (nutsedge, purple) ricegrass (barnyardgrass)
    LEFCH
    Leptochloa chinensis (L.) Nees
    SCPMA
    Schoenoplectus Maritimes (L.) Lye premature (watergrass, early) Chinese spring top (sprangletop, Chinese) sea rush (club rush, sea) g ae / ha = grams of acid equivalent per hectare g ai / ha = grams of active ingredient per hectare Obs = observed value
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    Exp = expected value as calculated using the Colby DAA equation = days after application
    Example III. Post-emergence Herbicidal Activity Assessment of Cereal Crops in the Greenhouse [0092] Seeds of the desired test plant species 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 about 30 percent, in plastic pots with a surface area of 103.2 square centimeters (cm 2 ). When necessary to ensure good germination and healthy plants, a fungicide treatment and / or other chemical or physical treatment was applied. The plants were grown for 7-36 days in a greenhouse with an approximate photoperiod of 14 hours that was maintained at about 18 ° C during the day and about 17 ° C at night. Nutrients and water were added on a regular basis and supplemental lighting was provided with 1000 Watt metal halide lamps suspended as needed. The plants were used for testing when they reached the second or third stage of true leaf.
    The treatments consisted of the benzyl ester of 4-amino-3-chloro-5-fluor-6- (4-chloro-2-fluor-3-methoxy-phenyl) pyridine-2-carboxylic acid (Compound A), formulated as a SC , a second cereal herbicide alone and then both in combination. The forms of compound A (compound of Formula I) tested include:
    Benzyl Ester of Compound A
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    81/94 [0093] Other herbicidal compounds were applied on an active ingredient basis and included microtubule inhibiting herbicides.
    [0094] Measured aliquots of benzyl ester of 4-amino-3-chloro-5-fluor-6- (4-chloro-2-fluor-3-methoxy-phenyl) pyridine-2-carboxylic acid (Compound A) were placed in 25 milliliter (mL) glass vials and diluted in a 1.25% (v / v) volume of Agri-Dex® culture oil concentrate to obtain stock solutions. The compost requirements are based on an application volume of 12 mL at a rate of 187 liters per hectare (L / ha). Spray solutions of the second cereal herbicide and mixtures of experimental compound were prepared by adding stock solutions to the appropriate amount of dilution solution to form 12 mL of spray solution with active ingredients in double and triple combinations. The formulated compounds were applied to the plant material with a suspended Mandel strip sprayer equipped with an 8002E calibrate nozzle to apply 187 L / ha in an application area of 0.503 square meters (m 2 ) at a spray height of 46 cm ( 18 inches) above the top of the average plant. Control plants were sprayed in the same way with solvent without activity.
    [0095] The treated plants and the control plants were placed in a greenhouse as described above and wetted by sub-irrigation to prevent run-off of the test compounds. After 20-22 days, the condition of the test plants compared to that of the control plants was determined visually and rated on a scale of 0 to 100 percent where 0 corresponds to no injury and 100 corresponds to complete death.
    [0096] 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.
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    Weeds 15: 20-22).
    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 in the same concentration as used in the mixture.
    B = observed effectiveness of active ingredient B at the same concentration as that used in the mixture.
    [0097] The tested compounds, application rates employed, plant species tested and results are given in Table 18.
    Table 18. Synergistic Activity of Benzyl Ester Compound and Herbicidal Composition of Pendimethalin Applied to Leaf on Weed Control in a Cereal Culture System.
    Benzyl Ester Compound Pendimethalin Visual Weed Control (%) - 21DAA AMARE CHEAL SINAR g ai / ha g ai / ha Note Exp Note Exp Note Exp 2.5 0 20 - 50 - 70 - 5 0 38 - 58 - 73 - 0 150 3 - 0 - 3 - 0 300 5 - 0 - 5 - 2.5 150 33 22 73 50 83 71 2.5 300 33 24 78 50 93 72 5 150 48 39 80 58 92 73 5 300 43 41 80 58 89 74
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    Benzyl Ester Compound Pendimethalin Visual Weed Control (%) - 21 DAA BRSNW CIRAR KCHSC g ai / ha g ai / ha Note Exp Note Exp Note Exp 2.5 0 18 - 48 - 20 - 5 0 13 - 39 - 41 - 10 0 13 - 60 - 62 - 0 150 3 - 10 - 10 - 0 300 5 - 10 - 10 - 0 600 18 - 10 - 57 - 2.5 150 30 20 48 53 63 28 2.5 300 48 22 60 53 78 28 5 150 38 15 68 45 55 47 5 300 50 17 65 45 73 47 5 600 72 29 70 45 80 74 10 600 85 29 85 64 85 83
    Compound AEster ofBenzila Pendimethalin Visual Weed Control (%) - 21DAA LAMP PAPRH STEME g ai / ha g ai / ha Note Exp Note Exp Note Exp 2.5 0 80 - 48 - 25 - 5 0 86 - 28 - 25 -
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    Compound AEster ofBenzila Pendimethalin Visual Weed Control (%) - 21DAA LAMP PAPRH STEME g ai / ha g ai / ha Note Exp Note Exp Note Exp 10 0 94 - 35 - 27 - 0 150 0 - 18 - 3 - 0 300 25 - 38 - 5 - 0 600 53 - 75 - 17 - 2.5 150 90 80 70 57 60 27 2.5 300 88 85 75 67 63 29 5 150 90 86 70 41 68 27 5 300 93 90 75 55 65 29 5 600 95 93 92 82 57 38 10 600 93 97 96 84 53 39
    AMARE Amaranthus retroflexus L. red root chenopod (pigweed, redroot) BRSNW Brassica napus winter rapeseed (rapeseed, winter) CHEAL Chenopodium album L. Common Anquinha (lambsquarters, common) CIRAR Cirsium arvense (L.) Scop. Canadian thistle (thistle, Canada) KCHSC Kochia scoparia (L.) Schrad. kochia LAMP Lamium purpureum L. dead nettle (deadnettle, purple) PAPRH Papaver rhoeas L. poppy (common)
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    SINAR Sinapis arvensis L.
    STEME Stellaria media (L.) Vill.
    wild mustard (chick mustard, common) g ae / ha = grams of acid equivalent per hectare g ai / ha = grams of active ingredient per hectare
    Obs = observed value
    Exp = expected value as calculated using the Colby DAA equation = days after application
    Example IV. Pre-emergence Evaluation of Herbicide Mixtures Applied to Soil for Weed Control [0098] Seeds or small nuts of the desired test plant species were planted in a soil matrix prepared by mixing a soil with mud (for example, 32 per cent of sediment, 23 per cent of clay and 45 per cent of sand, with a pH of about 6.5 and an organic matter content of about 1.9 per cent) and calcareous sand in an 80 to 20 ratio The soil matrix was contained in plastic pots with a volume of 1 quarter and a surface area of 83.6 square centimeters (cm 2 ).
    [0099] The treatments consisted of benzyl ester of 4 amino-3- chloro-5- fluorine- 6- (4-chloro-2-fluoro-3-methoxy-phenyl) pyridine-2-carboxylic acid (compound A) formulated as a SC (suspension concentrate) and various herbicidal components alone and in combination. Compound A forms were applied on an acid equivalent basis.
    [00100] The forms of compound A (compound of Formula I) tested included:
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    Benzyl Ester Compound [00101] Other herbicidal components were applied on an acid equivalent or active ingredient basis and included microtubule inhibiting herbicides, dithiopir formulated as Dithiopir 40WP, oryzaline formulated as Surflan®, pendimethalin formulated as Prow® 3.3EC , propizamide formulated as Kerb®50WP and thiazopyr (technical grade materials).
    [00102] Treatment needs 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.
    [00103] For treatments comprised of formulated compounds, measured amounts of compounds were individually placed in 25 mL glass bottles and diluted in a volume of 1.25% (v / v) of Agri-Dex® culture oil concentrate ( COC) to obtain 12X stock solutions. If a test compound did not readily dissolve, the mixture was heated and / or sonicated. Application solutions were prepared by adding an appropriate amount of each stock solution (eg 1 mL) and diluted to the appropriate final concentrations with the addition of 10 mL of a 1.25% (v / v) COC so that the final spray solutions contained 1.25% (v / v) COC. [00104] For treatments comprised of technical compounds, heavy quantities can be placed individually in vials of
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    87/94 25 mL glass and dissolved in a 97: 3 (v / v) volume of acetone / DMSO to obtain 12X stock solutions. If a test compound does not readily dissolve, the mixture can 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 a 1.5% (v / v) aqueous mixture of COC so that the final spray solutions contain 1.25% (v / v) COC. When technical materials are used, concentrated stock solutions can be added to the spray solutions so that the final concentrations of acetone and DMSO in the application solutions are 16.2% and 0.5%, respectively.
    [00105] For treatments comprised of formulated and technical compounds, heavy amounts of the technical materials were individually placed in 25 mL glass vials and dissolved in a 97: 3 (v / v) volume of acetone / DMSO to obtain stock solutions 12X and measured quantities of the formulated compounds were individually placed in 25 mL of glass vials and diluted in a volume of 1.5% (v / v) of COC or water to obtain 12X stock solutions. If a test compound did not readily dissolve, the mixture was heated and / or sonicated. 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 a 1.5% (v / v) aqueous mixture ) of COC so that the spray solutions contained 1.25% (v / v) of COC. As needed, more water and / or 97: 3 (v / v) acetone / DMSO was added to individual application solutions so that the final acetone and DMSO concentrations of the application solutions being compared were
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    8.1% and 0.25%, respectively.
    [00106] All stock solutions and application solutions were visually inspected for compound compatibility prior to application. The spray solutions were applied to the soil with a suspended Mandrel strip sprayer equipped with an 8002E nozzle calibrated to apply 187 L / ha in an application area of 0.503 m 3 at a spray height of 46 cm (18 inches) above the average pot height. Control pots were sprayed in the same way with the solvent without activity. [00107] Treated and control pots were placed in a greenhouse and irrigated from above as needed. When necessary to ensure plants with good germination and healthy, a treatment with fungicide and / or other chemical or physical treatment was applied. The pots were kept in a greenhouse with an approximate 14-hour photoperiod that was kept at around 29 ° C during the day and 26 ° C at night. Nutrients (Peters® Excel 15-5-15 5-Ca 2-Mg) were applied to the irrigation solution as needed and water was added on a regular basis. Supplementary lighting was provided with 1000 Watt metal halide lamps suspended as needed. After approximately 4 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.
    [00108] 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).
    [00109] The following equation was used to calculate the expected activity of mixtures containing two active ingredients, A and B:
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    Expected = A + B - (A x B / 100)
    A = observed effectiveness of active ingredient A in the same concentration as used in the mixture.
    B = observed effectiveness of active ingredient B at the same concentration as that used in the mixture.
    [00110] Some of the compounds tested, application rates employed, plant species tested and results are given in Tables 18-22.
    Table 18. Synergistic activity of Pre-emergence Applications, Applied to Soil, Benzyl Ester Compound and Dithiopir Herbicidal Compositions on Weed Control.
    Benzyl Ester Compound Dithiopir Visual Weed Control (%) -27 DAA IPOHE XANST g ae / ha g ai / ha Note Exp Note Exp 16 0 20 - 27 - 32 0 40 - 52 - 0 140 3 - 0 - 0 280 20 - 17 - 16 140 43 23 43 27 32 140 55 42 55 52 16 280 48 36 47 39 32 280 50 52 60 60
    Table 20. Synthetic Activity of Pre-emergence Applications, Applied to Soil, of Benzyl Ester Compound and Herbicidal Compositions of Orizaline in Weed Control.
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    Benzyl Ester Compound Orizalina Visual Weed Control (%)- 33 DAA IPOHE g ae / ha g ai / ha Note Exp 16 0 0 - 32 0 5 - 0 1120 48 - 16 1120 80 48 32 1120 95 51
    Table 21. Synergistic Activity of Pre-emergence Applications, Applied to Soil, of Benzyl Ester Compound and Herbicidal Compositions of Propizaride on Weed Control.
    Benzyl Ester Compound Propamide Visual Weed Control(%) - 33 DAA IPOHE g ae / ha g ai / ha Note Exp 16 0 0 - 32 0 5 - 0 1120 35 - 16 1120 70 35 32 1120 68 38
    Benzyl Ester Compound Propamide Visual Weed Control(%) - 33 DAA SEBEX g ae / ha g ai / ha Note Exp
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    Benzyl Ester Compound Propamide Visual Weed Control(%) - 33 DAA SEBEX g ae / ha g ai / ha Note Exp 16 0 40 - 0 280 20 - 0 560 13 - 0 1120 37 - 16 280 100 52 16 560 90 48 16 1120 95 62
    Benzyl Ester Compound Propamide Visual Weed Control(%) - 33 DAA BRAPP g ae / ha g ai / ha Note Exp 16 0 23 - 32 0 50 - 0 280 20 - 0 560 37 - 16 280 28 39 32 280 73 60 16 560 80 51 32 560 60 68
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    Benzyl Ester Compound Propamide Visual Weed Control(%) - 33 DAA ECHCG g ae / ha g ai / ha Note Exp 16 0 20 - 32 0 33 - 0 560 35 - 0 1120 53 - 16 560 98 48 32 560 50 57 16 1120 100 62 32 1120 100 69
    Benzyl Ester Compound Propamide Visual Weed Control l(%) - 33 DAA ECHCO SETFA g ae / ha g ai / ha Note Exp Note Exp 16 0 12 - 13 - 32 0 3 - 13 - 0 280 0 - 0 - 0 560 23 - 68 - 0 1120 80 - 93 - 16 280 5 12 50 13 32 280 60 3 88 13 16 560 55 32 100 73
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    Benzyl Ester Compound Propamide Visual Weed Control l(%) - 33 DAA ECHCOSETFA g ae / ha g ai / ha Note Exp Note Exp 32 560 70 26 55 73 16 1120 75 82 100 94 32 1120 100 81 100 94
    Table 22. Synergistic Activity of Pre-emergence Applications, Applied to Soil, of Benzyl Ester Compound and Herbicidal Compositions of Tiazopir on Weed Control
    Benzyl Ester Compound Tiazopir Visual Weed Control(%) - 27 DAA XANST g ae / ha g ai / ha Note Exp 16 0 10 - 32 0 25 - 0 280 15 - 0 560 10 - 16 280 40 24 16 560 35 19 16 1120 35 19
    BRAPP Brachiaria platyphylla (Groseb.) Nash or Urochloa platyphylla (Nash) R.D. Webster (broadleaf brachiaria (signalgrass, broadleaf)
    ECHCG Echinochloa crus-galli (L.) P. Beauv. rice grass (barnyardgrass)
    ECHCO Echinochloa colonum (L.) Link colony grass
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    94/94 (Junglerice)
    IPOHE kyll hederacea (L.) Jacq. jeticuçu (morningglory, ivyleaf)
    SEBEX Sesbania exaltata (Raf.) Cory / Rydb. Ex Hill sesbania, hemp
    SETFA Setaria faberi Herrm. giant foxtail (foxtail, giant)
    XANST Xanthium strumarium L. common thistle (cocklebur, common) g ae / ha = grams of acid equivalent per hectare g ai / ha = grams of active ingredient per hectare
    Obs = observed value
    Exp = expected value as calculated using the Colby equation
    DAA = days after application
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    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), or a benzyl ester or n-butyl ester thereof, and (b) a microtubule inhibiting herbicide selected from pendimethalin, dithiopir, thiazopyr, oryzaline or propizamide, when (a ) is a compound of Formula (I) or benzyl ester or n-butyl ester thereof and (b) is pendimethalin, the weight ratio from (a) to (b) is from 1: 8 to 1: 128;
    where (a) it is a compound of Formula (I) or benzyl ester thereof and (b) it is dithiopir, the weight ratio of (a) to (b) is from 1: 2 to 1:32;
    where (a) it is a benzyl ester of the compound of Formula (I) and (b) it is thiazopyr, the weight ratio of (a) to (b) is 1: 17.5, 1:35 and 1:70 ;
    where (a) it is a compound of Formula (I) or benzyl ester thereof and (b) it is oryzaline, the weight ratio from (a) to (b) is from 1:26 to 1: 256;
    where (a) it is a compound of Formula (I) or benzyl ester thereof and (b) it is propizaride, the weight ratio of (a) to (b) is from 1: 2 to 1:35.
    [2]
    2. Composition, according to claim 1, characterized by the fact that it also comprises an adjuvant or
    Petition 870190016610, of 02/19/2019, p. 4/10
    2/3 agriculturally acceptable vehicle.
    [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 stage of contacting a plant, the plant being an undesirable vegetation, or the location of the plant, soil or water, with soil or water allowing growth of undesirable vegetation, with a herbicidally effective amount of a composition, as defined in any one of claims 1 to 3.
    [5]
    5. Method, according to claim 4, characterized by the fact that the unwanted vegetation is controlled in rice sown directly, sown in water and transplanted, cereals, wheat, barley, oats, rye, sorghum, corn, cane -sugar, sunflower, rapeseed, canola, sugar beet, soy, cotton, pineapple, grass for pasture, grassland, pasture, fallow, grass, tree and vine orchards, aquatic, industrial vegetation management (IVM) or easements ( ROW).
    [6]
    6. Method according to claim 4 or 5, characterized by the fact that (a) and (b) are applied preemergently to the plant or crop.
    [7]
    Method according to any one of claims 4 to 6, characterized in that the unwanted vegetation is controlled in glyphosate-tolerant cultures, 5enolpyruvylshiquimato-3-phosphate (EPSP) synthase, glufosinate, glutamine synthase inhibitor, dicamba, phenoxy auxin, pyridyloxy auxin, synthetic auxin, auxin transport inhibitor, aryloxyphenoxypropionate, cyclohexanedione, phenylpyrazoline, acetyl CoA carboxylase (ACCase) inhibitor, imidazolinone, sulfonylurea, pyrimidinylthiobenzoate,
    Petition 870190016610, of 02/19/2019, p. 5/10
    3/3 triazolpyrimidine, sulfonylaminocarbonyltriazolinone, acetolactate synthase (ALS) or acetohydroxy acid synthase (AHAS) inhibitors, 4-hydroxyphenyl-pyruvate dioxigenase (HPPD) inhibitor, phytene desaturase inhibitor, carotene oxide inhibitor (carotene oxide inhibitor) , cellulose synthesis inhibitor, mitosis inhibitor, microtubule inhibitor, very long chain fatty acid inhibitor, fatty acid and lipid biosynthesis inhibitor, photosystem I inhibitor, photosystem II inhibitor, triazine or bromoxynil.
    [8]
    8. Method, according to claim 7, characterized by the fact that the tolerant culture has multiple or stacked characteristics conferring tolerance to multiple herbicides or multiple modes of action.
    [9]
    Method according to any one of claims 4 to 8, characterized in that the vegetation comprises a herbicide resistant or tolerant plant.
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    同族专利:
    公开号 | 公开日
    US20140031219A1|2014-01-30|
    RU2017128076A|2019-02-01|
    RU2629255C2|2017-08-28|
    KR20150038247A|2015-04-08|
    HK1209586A1|2016-04-08|
    CN104661519A|2015-05-27|
    PT2877016T|2019-04-18|
    US9119397B2|2015-09-01|
    AU2013293311B2|2017-04-06|
    JP2015527329A|2015-09-17|
    CA2879951A1|2014-01-30|
    EP2877016A1|2015-06-03|
    AR091899A1|2015-03-11|
    US20150018208A1|2015-01-15|
    US8846570B2|2014-09-30|
    UY34933A|2014-02-28|
    SA113340754B1|2015-07-07|
    JP6220875B2|2017-10-25|
    AU2013293311A1|2015-03-05|
    WO2014018398A1|2014-01-30|
    SG11201500531UA|2015-02-27|
    CN104661519B|2017-06-06|
    BR102013018481A2|2015-03-03|
    IL236864A|2019-07-31|
    ES2713171T3|2019-05-20|
    EP2877016A4|2016-03-16|
    MX2015001157A|2016-07-07|
    ZA201501147B|2017-07-26|
    KR102102408B1|2020-04-20|
    IN2015DN01376A|2015-07-03|
    RU2015105741A|2016-09-10|
    TWI627905B|2018-07-01|
    TW201406296A|2014-02-16|
    IL236864D0|2015-03-31|
    SA115360505B1|2016-01-14|
    EP2877016B1|2018-12-26|
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    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]|
    2015-05-05| B03H| Publication of an application: rectification [chapter 3.8 patent gazette]|Free format text: REFERENTE A RPI 2304 DE 03/03/2015, QUANTO AO ITEM (57). |
    2016-10-11| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2018-09-11| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]|
    2019-01-08| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]|
    2019-04-09| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2019-06-18| 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. (CO) 20 (VINTE) ANOS CONTADOS A PARTIR DE 19/07/2013, OBSERVADAS AS CONDICOES LEGAIS |
    优先权:
    申请号 | 申请日 | 专利标题
    US201261675100P| true| 2012-07-24|2012-07-24|
    US61/675.100|2012-07-24|
    US13/840.303|2013-03-15|
    US13/840,303|US8846570B2|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 microtubule inhibiting herbicides|
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