AU2015203090A1 - Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops - Google Patents

Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops Download PDF

Info

Publication number
AU2015203090A1
AU2015203090A1 AU2015203090A AU2015203090A AU2015203090A1 AU 2015203090 A1 AU2015203090 A1 AU 2015203090A1 AU 2015203090 A AU2015203090 A AU 2015203090A AU 2015203090 A AU2015203090 A AU 2015203090A AU 2015203090 A1 AU2015203090 A1 AU 2015203090A1
Authority
AU
Australia
Prior art keywords
herbicide
amino
formula
pyridinecarboxylate
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
AU2015203090A
Other versions
AU2015203090B2 (en
Inventor
Norbert Satchivi
Paul Schmitzer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Corteva Agriscience LLC
Original Assignee
Dow AgroSciences LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from AU2009316667A external-priority patent/AU2009316667B2/en
Application filed by Dow AgroSciences LLC filed Critical Dow AgroSciences LLC
Priority to AU2015203090A priority Critical patent/AU2015203090B2/en
Publication of AU2015203090A1 publication Critical patent/AU2015203090A1/en
Application granted granted Critical
Publication of AU2015203090B2 publication Critical patent/AU2015203090B2/en
Assigned to CORTEVA AGRISCIENCE LLC reassignment CORTEVA AGRISCIENCE LLC Request to Amend Deed and Register Assignors: DOW AGROSCIENCES, LLC
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

P/0/01l Regulation 3.2 AUSTRALIA Patents Act 1990 COMPLETE SPECIFICATION STANDARD PATENT Invention Title: Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops The following statement is a full description of this invention, including the best method of performing it known to us: SAFENING 6-(TRISUBSTITUTED PHENYL)-4-AMINO-2-PYRIDINECARBOXYLATE HERBICIDE INJURY ON CEREAL CROPS This application claims the benefit of United States Provisional Application Serial Number 61/117,332 filed on November 24, 2008. This invention concerns the safening of the 5 herbicidal injury caused by 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylates in cereal crops. When agrochemicals, such as plant protection agents and especially herbicides, are used, the cultivated plants may be damaged to a certain degree, depending on factors such as the dose of agrochemicals and their method of application, the species of cultivated plant, the 10 nature of the soil and climatic conditions, for example, length of time of exposure to light, temperature and amounts of precipitation. Thus, it is known that cultivated plants which are to be protected from the adverse effect of undesirable plant growth may be damaged to a certain degree when an effective dose of herbicide is used. Various substances which are capable of specifically preventing the adverse effect of an herbicide on the cultivated plants, 15 i.e. of protecting the cultivated plants without at the same time noticeably influencing the herbicidal action on weeds to be combated, have been proposed to solve this problem. However, it has been found that the antidotes proposed frequently have only a narrow field of use, i.e., a particular antidote is frequently suitable only for use with individual species of cultivated plants and/or for protecting the cultivated plants from individual herbicidal 20 substances or classes of substances. U.S. Patent 7,314,849 B2 describes certain 6-(polysubstituted aryl)-4-amino-2 pyridinecarboxylate compounds and their use as herbicides. While certain of these compounds have been shown to be particularly effective herbicides for controlling undesirable vegetation in cereal crops, they have also been shown to produce slight amounts 25 of damage to both wheat and barley at concentrations required to adequately control the undesirable vegetation. It has now been found that, surprisingly, the phytotoxic effect of certain 6-(poly substituted aryl)-4-amino-2-pyridinecarboxylate compounds, which have an auxinic mode of action, on wheat and barley can be ameliorated by the use of certain safeners. The present 30 invention concerns a method of protecting cereal crops from the harmful effects of a 6 (trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide of the formula (I) 1 /\ NH(2 hal OH N 0 hal hal OR g wherein hal represents F, Cl or Br, and R represents methyl or ethyl, and its agriculturally acceptable salt, ester and amide derivatives which comprises contacting wheat and barley with, or applying to the area under cultivation, a safener, or a compatible 5 herbicide capable of safening, selected from the group consisting of AD67 (MON 4660), benoxacor, 2-CBSU, daimuron, dichlormid, dicyclonon (BAS 145 138H), fenchlorazole ethyl, fenclorim, fluxofenim, furilazole (MON 13900), glyphosate, isoxadifen-ethyl, mefenpyr-diethyl, naphthalic anhydride, oxabetrinil and mixtures thereof. The present invention also concerns a composition for protecting wheat and barley 10 from the harmful effects of a 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide of the formula (I) NH2 hal OH N 0 hal hal OR (1) wherein hal represents F, Cl or Br, and R represents methyl or ethyl, and its agriculturally acceptable salt, ester and amide derivatives which comprises, in addition 15 to the 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide, a safener or compatible herbicide capable of safening selected from the group consisting of AD67 (MON4660), benoxacor, 2-CBSU, daimuron, dichlormid, dicyclonon (BAS 145 138H), fenchlorazole-ethyl, fenclorim, fluxofenim, furilazole (MON 13900), glyphosate, isoxadifen ethyl, mefenpyr-diethyl, naphthalic anhydride, oxabetrinil, and mixtures thereof. In preferred 2 compositions, the 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide is a 4 amino-3 -chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-2-pyridinecarboxylic acid derivative or a 4-amino-3-chloro-6-(2,4-dichloro-3-methoxyphenyl)-2-pyridinecarboxylic acid derivative. 5 It has been surprisingly found that the use of a spirooxazolidine safener such as AD 67 (MON 4660) in composition with a pyridinecarboxylate herbicide of the formula (I) exhibits a protecting effect against the phytotoxicity of the pyridinecarboxylate herbicide of formula (I) on wheat (Triticum aestivum L; TRZAS) and barley (Hordeun vulgare L; HORVS) without losing the herbicidal effects on weeds such as cleavers (Galium aparine L; 10 GALAP), purple deadnettle (Lamium purpureum L; LAMPU), corn poppy (Papaver rhoeas L; PAPRH). The combinations of dichloroacetamide safeners such as benoxacor, dichlormid, dicyclonon (BAS 145 138H), furilazole (MON 13900) and a pyridinecarboxylate herbicide of formula (I) resulted in an unexpected safening effect against the phytotoxicity of the 15 pyridinecarboxylate herbicide of formula (I) on wheat (Triticum aestivum L; TRZAS) and barley (Hordeum vulgare L; HORVS) without reduction of the herbicidal effects on weeds such as cleavers (Galium aparine L; GALAP), purple deadnettle (Lamium purpureum L; LAMPU), corn poppy (Papaver rhoeas L; PAPRH), chickweed (Stellaria media L; STEME), bird's-eye speedwell (Veronica persica L; VERPE). 20 It has also been surprisingly found that a mixture of a benzenesulfonamide safener such as 2-CBSU and a pyridinecarboxylate herbicide of formula (I) exhibits a safening effect against the phytotoxicity of the pyridinecarboxylate herbicide of formula (I) on wheat (Triticun aestivum L; TRZAS) and barley (Hordeum vulgare L; HORVS) without losing the herbicidal effects on weeds such as cleavers (Galium aparine L; GALAP), purple deadnettle 25 (Lamium purpureum L; LAMPU), corn poppy (Papaver rhoeas L; PAPRH). It has also been unexpectedly found that the mixture of phenyl pyrazole safeners such as fenchlorazole-ethyl, mefenpyr-diethyl and a pyridinecarboxylate herbicide of formula (I) shows a safening effect against the phytotoxicity of the pyridinecarboxylate herbicide of formula (I) on wheat (Triticum aestivum L; TRZAS) and barley (Hordeun vulgare L; 30 HORVS) without reducing the herbicidal effects on weeds such as cleavers (Galium aparine L; GALAP), purple deadnettle (Lamium purpureum L; LAMPU), corn poppy (Papaver 3 rhoeas L; PAPRH), bird's-eye speedwell (Veronica persica L; VERPE), Russian thistle (Salsola iberica L; SASKR), wild pansy (Viola tricolor L; VIOTR). The combination of a phenylpyrimidine safener such as fenclorim and a pyridinecarboxylate herbicide of formula (I) exhibits a safening effect against the 5 phytotoxicity of the pyridinecarboxylate herbicide of formula (I) on wheat (Triticum aestivun L; TRZAS) and barley (Hordeum vulgare L; HORVS) without losing the herbicidal effects on weeds such as cleavers (Galium aparine L; GALAP), purple deadnettle (Laniuni purpureun L; LAMPU), corn poppy (Papaver rhoeas L; PAPRH), wild buckwheat (Polygonun convolvulus L; POLCO). 10 The combinations of safeners of the oxime class such as fluxofenim, oxabetrinil and a pyridinecarboxylate herbicide of formula (I) have resulted in an unexpected safening effect against the phytotoxicity of the pyridinecarboxylate herbicide of formula (I) on wheat (Triticum aestivum L; TRZAS) and barley (Hordeum vulgare L; HORVS) without reduction of the herbicidal effects on weeds such as cleavers (Galiun aparine L; GALAP), purple 15 deadnettle (Lanium purpureum L; LAMPU), corn poppy (Papaver rhoeas L; PAPRH), scented mayweed (Matricaria chamomila L; MATCH), Russian thistle (Salsola iberica L; SASKR). It has also been surprisingly found that the mixture of oxime ether safeners, such as isoxadifen-ethyl, and a pyridinecarboxylate herbicide of formula (I) shows a safening effect 20 against the phytotoxicity of the pyridinecarboxylate herbicide of formula (I) on wheat (Triticum aestivun L; TRZAS), durum wheat (Triticun durum L; TRZDU), and barley (Hordeun vulgare L; HORVS) without reducing the herbicidal effects on weeds such as purple deadnettle (Lamium purpureun L; LAMPU), corn poppy (Papaver rhoeas L; PAPRH). 25 The mixture of a naphthopyranone safener such as naphthalic anhydride and a pyridinecarboxylate herbicide of formula (I) shows an unexpected safening effect against the phytotoxicity of the pyridinecarboxylate herbicide of formula (I) on wheat (Trilicum aestivun L; TRZAS) and barley (Hordeurn vulgare L; HORVS) without reduction of the herbicidal effects on weeds such as cleavers (Galiun aparine L; GALAP), purple deadnettle (Lamium 30 purpureun L; LAMPU), corn poppy (Papaver rhoeas L; PAPRH), kochia (Kochia scoparia L; KCHSC), wild pansy (Viola tricolor L; VIOTR). 4 It has also been unexpectedly found that the mixture of a pyridinecarboxylate herbicide of formula (I) and a phenylurea herbicide such as daimuron exhibits a surprising safening effect against the phytotoxicity of the pyridinecarboxylate herbicide of formula (I) on wheat (Triticum aestivum L; TRZAW), durum wheat (Triticum durum L; TRZDU), and 5 barley (Hordeum vulgare L; HORVS) without reducing the herbicidal effects on weeds such as purple deadnettle (Lamium purpureuin L; LAMPU), corn poppy (Papaver rhoeas L; PAPR H). It has been also surprisingly found that the mixture of a pyridinecarboxylate herbicide of the formula (I) and an EPSP (5-enolpyruvylshikimate-3-phosphate) synthase inhibitor 10 herbicide such as glyphosate exhibits an unexpected safening effect against the phytotoxicity on wheat (Triticum aestivun L; TRZAS) and barley (Hordeum vulgare L; HORVS). The pyridinecarboxylates of formula I are a new class of compounds having herbicidal activity. A number of pyridinecarboxylate compounds are described in U.S. Patent 7,314,849, including 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2 15 carboxylic acid (compound 1) and 4-amino-3-chloro-6-(2,4-dichloro-3-methoxyphenyl) pyridine-2-carboxylic acid (compound 2). The pyridinecarboxylates of formula (I) control annual grass weeds and broadleaf weeds in wheat and barley but are also phytotoxic to wheat and barley at commercially herbicidal doses. AD67 (MON 4660) is the common name for 4-(dichloroacetyl)- 1 -oxa-4 20 azaspiro[4,5]decane. Its safening activity is described in The Pesticide Manual, Thirteenth Edition, 2003. AD67 (MON 4660) is used as a safener in maize. Benoxacor is the common name for (±)-4-(dichloroacetyl)-3,4-dihydro-3-methyl-2H 1,4-benzoxazine. Its safening activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Benoxacor is used as a safener in maize. 25 2-CBSU is the common name for N-(aminocarbonyl)-2-chlorobenzenesulfonamide. Its safening activity is described in Modern Crop Protection Compounds, 2007. 2-CBSU has been shown to safen herbicidal injury in maize. Daimuron is the common name for N-(4-methylphenyl)-N'-(1-methyl-1 phenylethyl)urea. Its herbicidal activity is described in The Pesticide Manual, Fourteenth 5 Edistion, 2006. Daimuron is used as a selective herbicide of cyperaceous weeds and annual grass weeds in paddy rice. Dichlormid is the common name for NN-diallyl-2,2-dichloroacetamide. Its safening activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Dichlormid is used 5 as a safener for maize and sorghum. Dicyclonon (BAS 145 138H) is the common name for (RS)-1-dichloroacetyl-3,3,8a trimethylperhydropyrrolo[1,2]pyrimidin-6-one. Its safening activity is described in Pesticide Biochemistry and Physiology 1992, 42, 128-139. Dicyclonon (BAS 145 138H) is used as a safener for maize. 10 Fenchlorazole is the common name for 1-(2,4-dichlorophenyl)-5-(trichloromethyl) 1H-1,2,4-triazole-3-carboxylic acid. Its safening activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Fenchlorazole is used as a safener in wheat, rye and triticale. Fenclorim is the common name for 4,6-dichloro-2-phenylpyrimidine. Its safening 15 activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Fenclorim is used as a safener in direct-seeded rice. Fluxofenim is the common name for 1-(4-chlorophenyl)-2,2,2-trifluoroethanone 0 (1,3-dioxolan-2-ylmethyl)oxime. Its safening activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Fluxofenim is used as a safener in sorghum. 20 Furilazole (MON 13900) is the common name for 3-(dichloroacetyl)-5-(2-furanyl) 2,2-dimethyloxazolidine. Its safening activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Furilazole (MON 13900) is used as a safener in maize. Isoxadifen-ethyl is the common name for ethyl 4,5-dihydro-5,5-diphenyl-3 isoxazolecarboxylate. Its safening activity is described in The Pesticide Manual, Fourteenth 25 Edition, 2006. Isoxadifen is used as a safener in maize. Glyphosate is the common name for N-(phosphonomethyl)glycine. Its herbicidal activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Glyphosate controls a wide range of annual and perennial, broadleaf and grass weeds. 6 Mefenpyr is the common name for 1-(2,4-dichlorophenyl)-4,5-dihydro-5-methyl-1H pyrazole-3,5-dicarboxylic acid. Its safening activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Mefenpyr is used as a safener in wheat, rye, triticale and barley. Naphthalic anhydride is the common name for 1H,3H-naphtho[l,8-cdlpyran-l,3 5 dione. Its safening activity is described in The Pesticide Manual, Eighth Edition, 1987. Naphthalic anhydride is used as a safener in maize and sorghum. Oxabetrinil is the common name for o.-[(1,3-dioxolan-2-yl)methoxyimino]benzene acetonitrile. Its safening activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Oxabetrinil is used as a safener in sorghum. 10 The term herbicide is used herein to mean an active ingredient that kills, controls or otherwise adversely modifies the growth of plants. An herbicidally effective or vegetation controlling amount is an amount of active ingredient which causes an adversely modifying effect and includes deviations from natural development, killing, regulation, desiccation, retardation, and the like. The terms plants and vegetation include germinant seeds, emerging 15 seedlings and established vegetation. The term safener, as used herein, refers to a compound that selectively protects crop plants from herbicide damage without significantly reducing activity in target weed species. Herbicidal activity is exhibited by the compounds when they are applied directly to the plant or to the locus of the plant via foliar, soil, or water application at any stage of 20 growth or before planting or emergence. The effect observed depends upon the plant species to be controlled, the stage of growth of the plant, the application parameters of dilution and spray drop size, the particle size of solid components, the environmental conditions at the time of use, the specific compound employed, the specific adjuvants and carriers employed, the soil type, and the like, as well as the amount of chemical applied. These and other factors 25 can be adjusted as is known in the art to promote non-selective or selective herbicidal action. Generally, it is preferred to apply the composition of the present invention postemergence to relatively immature undesirable vegetation to achieve the maximum control of weeds. Cultivated plants which are to be protected from the adverse effect of undesirable plant growth may be damaged to a certain degree when an effective dose of herbicides is 30 used. Safening means preventing the adverse effect of an herbicide on the cultivated plants, 7 i.e., protecting the cultivated plants without, at the same time, noticeably influencing the herbicidal action on weeds to be combated. In the composition of this invention, the weight ratio of the safener to the pyridinecarboxylate of formula (I) at which the herbicidal effect on the cultivated plant is 5 safened lies within the range of between 16:1 and 1:32. Preferably, the weight ratio of the safener to the pyridinecarboxylate of formula (I) at which the herbicidal effect on the cultivated plant is safened lies within the range of between 4:1 and 1:8. The rate at which the safened composition is applied will depend upon the particular type of weed to be controlled, the degree of control required, and the timing and method of 10 application. In general, the composition of the invention can be applied at an application rate of between 4 grams per hectare (g/ha) and 1200 g/ha based on the total amount of pyridinecarboxylate of formula (I) and safener in the composition. The pyridinecarboxylate of formula (I) and the safener of the present invention can be applied either separately or together as part of a multipart herbicidal system. 15 The herbicide-safener mixture of the present invention can be applied in conjunction with one or more other herbicides to control a wider variety of undesirable vegetation. When used in conjunction with other herbicides, the composition can be formulated with the other herbicide or herbicides, tank mixed with the other herbicide or herbicides or applied sequentially with the other herbicide or herbicides. Some of the herbicides that can be 20 employed in conjunction with the safened composition of the present invention include: 2,4 D esters and amines, acetochlor, acifluorfen, aclonifen, AE0172747, alachlor, aminocyclopyrachlor, amidosulfuron, aminotriazole, ammonium thiocyanate, anilifos, atrazine, AVH 301, azimsulfuron, benfuresate, bensulfuron-methyl, bentazone, benthiocarb, benzobicyclon, bifenox, bispyribac-sodium, bromacil, bromoxynil, butachlor, butafenacil, 25 butralin, cafenstrole, carbetamide, carfentrazone-ethyl, chlorflurenol, chlorimuron, chlorpropham, cinosulfuron, clethodim, clomazone, clopyralid, cloransulam-methyl, cyclosulfamuron, cycloxydim, cyhalofop-butyl, dicamba, dichlobenil, dichlorprop-P, diclosulam, diflufenican, diflufenzopyr, dimethenamid, dimethenamid-p, diquat, dithiopyr, diuron, EK2612, EPTC, esprocarb, ET-751, ethoxysulfuron, ethbenzanid, F7967, fenoxaprop, 30 fenoxaprop-ethyl, fentrazamide, flazasulfuron, florasulam, fluazifop, fluazifop-P-butyl, flucetosulfuron, flufenacet, flufenpyr-ethyl, flumetsulam, flumiclorac-pentyl, flumioxazin, 8 fluometuron, flupyrsulfuron, fluroxypyr, fomesafen, foramsulfuron, fumiclorac, glufosinate, glufosinate-ammonium, glyphosate, halosulfuron, haloxyfop-methyl, haloxyfop-R, imazamethabenz, imazamox, imazapic, imazapyr, imazaquin, imazethapyr, imazosulfuron, indanofan, iodosulfuron, ioxynil, IR 5790, isoproturon, isoxaben, isoxaflutole, KUH-021, 5 lactofen, linuron, MCPA, MCPA ester & amine, mecoprop-P, mefenacet, mesosulfuron, mesotrione, metamifop, metolachlor, metosulan, metribuzin, metsulfuron, molinate, MSMA, napropamide, nicosulfuron, norflurazon, OK-9701, orthosulfamuron, oryzalin, oxadiargyl, oxadiazon, oxazichlomefone, oxyfluorfen, paraquat, pendimethalin, penoxsulam, pentoxazone, pethoxamid, picloram, picolinafen, piperophos, pretilachlor, profoxydim, 10 propachlor, propanil, propyzamide, prosulfocarb, prosulfuron, pyraclonil, pyrasulfotole, pyrazogyl, pyrazosulfuron, pyribenzoxim, pyriftalid, pyriminobac-methyl, primisulfuron, pyroxsulam, quinclorac, quizalofop-ethyl-D, S-3252, saflufenacil, sethoxydim, simazine, SL 0401, SL-0402, s-metolachlor, sulcotrione, sulfentrazone, sulfosate, tebuthiuron, terbacil, TH-547, thiazopyr, thiobencarb, triclopyr, triclopyr esters and amine, trifluralin and 15 tritosulfuron. The safened composition of the present invention can, further, be used in conjunction with glyphosate, glufosinate, dicamba, imidazolinones or 2,4-D on glyphosate-tolerant, glufosinate-tolerant, dicamba-tolerant, imidazolinone-tolerant or 2,4-D-tolerant crops. It is generally preferred to use the herbicide-safener mixture of the present invention in 20 combination with herbicides that are selective for the crop being treated and which complement the spectrum of weeds controlled by these compounds at the application rate employed. It is further generally preferred to apply the safened composition of the present invention and other complementary herbicides at the same time, either as a combination formulation or as a tank mix. 25 In practice, it is preferable to use the safened composition of the present invention in mixtures containing an herbicidally effective amount of the herbicidal components along with at least one agriculturally acceptable adjuvant or carrier. Suitable adjuvants or carriers should not be phytotoxic to valuable crops, particularly at the concentrations employed in applying the compositions for selective weed control in the presence of crops, and should not react 30 chemically with herbicidal components or other composition ingredients. Such mixtures can be designed for application directly to weeds or their locus or can be concentrates or formulations that are normally diluted with additional carriers and adjuvants before 9 application. They can be solids, such as, for example, dusts, granules, water dispersible granules, or wettable powders, or liquids, such as, for example, emulsifiable concentrates, solutions, emulsions or suspensions. Suitable agricultural adjuvants and carriers that are useful in preparing the herbicidal 5 mixtures of the invention are well known to those skilled in the art. Some of these adjuvants include, but are not limited to, crop oil concentrate (mineral oil (85%) + emulsifiers (15%)); nonylphenol ethoxylate; benzylcocoalkyldimethyl quaternary ammonium salt; blend of petroleum hydrocarbon, alkyl esters, organic acid, and anionic surfactant; C 9 -Cnl alkylpolyglycoside; phosphated alcohol ethoxylate; natural primary alcohol (C12-Ci6) 10 ethoxylate; di-sec-butylphenol EO-PO block copolymer; polysiloxane-methyl cap; nonylphenol ethoxylate + urea ammonium nitrate; emulsified methylated seed oil; tridecyl alcohol (synthetic) ethoxylate (8EO); tallow amine ethoxylate (15 EO); PEG(400) dioleate 99. Liquid carriers that can be employed include water, toluene, xylene, petroleum 15 naphtha, crop oil, acetone, methyl ethyl ketone, cyclohexanone, trichloroethylene, perchloroethylene, 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, glycerine, N-methyl-2 pyrrolidinone, NN-dimethyl alkylamides, dimethyl sulfoxide, liquid fertilizers and the like. 20 Water is generally the carrier of choice for the dilution of concentrates. Suitable solid carriers include talc, pyrophyllite clay, silica, attapulgus clay, kaolin clay, kieselguhr, chalk, diatomaceous earth, lime, calcium carbonate, bentonite clay, Fuller's earth, cotton seed hulls, wheat flour, soybean flour, pumice, wood flour, walnut shell flour, lignin, and the like. 25 It is usually desirable to incorporate one or more surface-active agents into the compositions of the present invention. Such surface-active agents are advantageously employed in both solid and liquid compositions, especially those designed to be diluted with carrier before application. The surface-active agents can be anionic, cationic or nonionic in character and can be employed as emulsifying agents, wetting agents, suspending agents, or 30 for other purposes. Surfactants conventionally used in the art of formulation and which may also be used in the present formulations are described, inter alia, in "McCutcheon's 10 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. Typical surface-active agents include salts of alkyl sulfates, such as diethanolammonium lauryl sulfate; alkylarylsulfonate salts, such as calcium dodecylbenzenesulfonate; 5 alkylphenol-alkylene oxide addition products, such as nonylphenol-Cis ethoxylate; alcohol-alkylene oxide addition products, such as tridecyl alcohol-C 16 etboxylate; soaps, such as sodium stearate; alkylnaphthalene-sulfonate salts, such as sodium dibutyl naphthalenesulfonate; dialkyl esters of sulfosuccinate salts, such as sodium di(2-ethylhexyl) sulfosuccinate; sorbitol esters, such as sorbitol oleate; quaternary amines, such as lauryl 10 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 oils such as soybean oil, rapeseed oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cotton seed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, tung oil and the like; and esters of the above vegetable oils. 15 Other additives commonly used in agricultural compositions include compatibilizing agents, antifoam agents, sequestering agents, neutralizing agents and buffers, corrosion inhibitors, dyes, odorants, spreading agents, penetration aids, sticking agents, dispersing agents, thickening agents, freezing point depressants, antimicrobial agents, and the like. The compositions may also contain other compatible components, for example, other herbicides, 20 plant growth regulants, fungicides, insecticides, and the like and can be formulated with liquid fertilizers or solid, particulate fertilizer carriers such as ammonium nitrate, urea and the like. The concentration of the active ingredients in the herbicide-safener mixture of the present invention is generally from 0.001 to 98 percent by weight. Concentrations from 0.01 25 to 90 percent by weight are often employed. In compositions designed to be employed as concentrates, the active ingredients are generally present in a concentration from 5 to 98 weight percent, preferably 10 to 90 weight percent. Such compositions are typically diluted with an inert carrier, such as water, before application. The diluted compositions usually applied to weeds or the locus of weeds generally contain 0.0001 to I weight percent active 30 ingredient and preferably contain 0.001 to 0.05 weight percent. 11 The present compositions can be applied to weeds or their locus by the use of conventional ground or aerial dusters, sprayers, and granule applicators, or irrigation water, and by other conventional means known to those skilled in the art. The following examples illustrate the present invention. 5 Evaluation of Postemergence Herbicidal Safening in Cereal Crops Seeds of the desired test plant species were planted in 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 pots with a surface area of 103.2 square centimeters (cm 2 ). When required to ensure good germination and healthy plants, a fungicide treatment and/or other chemical or 10 physical treatment was applied. The plants were grown for 7-36 days (d) in a greenhouse with an approximate 14-hour (h) photoperiod which was maintained at 18 'C during the day and 17 'C during the night. Nutrients and water were added on a regular basis and supplemental lighting was provided with overhead metal halide 1000-Watt lamps as necessary. The plants were employed for testing when they reached the second or third true 15 leaf stage. Weighed amounts of esters (methyl) or salts (TEA [triethylammonium], K [potassium]) of 4-amino-3-chloro-6-(4-chloro-2-fluoro- 3 -methoxyphenyl)pyridine-2 carboxylic acid (Compound 1) were dissolved in a volume of 97:3 volume/volume (v/v) acetone/dimethylsulfoxide (DMSO) to obtain stock solutions. If the experimental compound 20 did not dissolve readily, the mixture was warmed and/or sonicated. The concentrated stock solutions were diluted with an aqueous mixture of 1.5% v/v of Agri-dex crop oil concentrate to provide the appropriate application rates. Compound requirements are based upon a 12 mL application volume at a rate of 187 liters per hectare (L/ha). Stocks solutions of the safeners were prepared following the same procedure. Spray solutions of the safeners and 25 experimental compound mixtures were prepared by adding the stock solutions to the appropriate amount of dilution solution to form a 12 mL spray solution with active ingredients in two-way combinations. Formulated compounds were applied to the plant material with an overhead Mandel track sprayer equipped with 8002E nozzles calibrated to deliver 187 L/ha over an application area of 0.503 square meters (M) at a spray height of 18 30 inches (43 centimeters (cm)) above average plant canopy. Control plants were sprayed in the same manner with the solvent blank. 12 The treated plants and control plants were placed in a greenhouse as described above and watered by sub-irrigation to prevent wash-off of the test compounds. After 20-22 d, the condition of the test plants as compared with that of the control plants was determined visually and scored on a scale of 0 to 100 percent where 0 corresponds to no injury and 100 5 corresponds to complete kill. Colby's equation was used to determine the herbicidal effects expected from the mixtures (Colby, S.R. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 1967, 15, 20-22.). The following equation was used to calculate the expected activity of mixtures 10 containing two active ingredients, A and B: Expected = A + B - (A x B/100) A = observed efficacy of active ingredient A at the same concentration as used in the mixture. B = observed efficacy of active ingredient B at the same concentration as used in the 15 mixture. Some of the compounds tested, application rates employed, plant species tested, and results are given in Table I through Table 22. 13 Table 1. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g/ha) TRZAS HORVS GALAP KCHSC LAMPU MATCH Herbicide: Compound AD67 Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex 1 TEA salt Ratio 140 0 26 - 16 - 100 - 94 - 99 - 80 0 140 0 - 0 - 0 - 0 70 0 - 0 - 0 - - 0 35 0 - 0 - 0 - 0 17.5 0 - 0 - 0 - 140 140 1:1 10 26 6 16 100 100 83 94 100 99 80 80 140 70 2:1 11 26 9 16 100 100 75 94 99 99 63 80 140 35 4:1 10 26 0 16 100 100 95 94 99 99 73 80 Application Rate (g/ha) PAPRH POLCO SASKR STEME VERPE VIOTR Herbicide: Compound AD67 Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex 1 TEA salt Ratio 140 0 100 - 100 - 88 - 94 - 85 - 69 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 100 100 100 100 85 88 88 94 89 85 58 69 140 70 2:1 100 100 93 100 83 88 100 94 89 85 68 69 140 35 4:1 100 100 88 100 85 88 100 94 88 85 65 69 14 Table 2. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g/ha) TRZAS HORVS GALAP KCHSC LAMPU MATCH Herbicide: Compound Benoxacor Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex 1 TEA salt Ratio 140 0 26 - 16 - 100 - 94 - 99 - 80 0 140 0 - 0 - 0 - 0 70 0 - 0 - 0 - 0 35 0 - 0 - 0 - 0 17.5 0 - 0 - 0 - 140 140 1:1 7 26 5 16 100 100 91 94 100 99 78 80 140 70 2:1 14 26 7 16 100 100 96 94 100 99 90 80 140 35 4:1 20 26 0 16 100 100 96 94 100 99 80 80 Application Rate (g/ha) PAPRH POLCO SASKR STEME VERPE VIOTR Compound Herbicide: CompoundtBenoxacor Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex 1 TEA salt Ratio 140 0 100 - 100 - 88 - 94 - 85 - 69 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 100 100 98 100 85 88 99 94 85 85 78 69 140 70 2:1 100 100 98 100 85 88 95 94 80 85 65 69 140 35 4:1 100 100 98 100 85 88 99 94 83 85 65 69 15 Table 3. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g/ha) TRZAS HORVS GALAP KCHSC LAMPU MATCH Compound 2Herbicide: 2-CBSU Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ratio 140 0 26 - 16 - 100 - 94 - 99 - 80 0 140 0 - 0 - 0 - 0 70 0 - 0 - 0 0 35 0 - 0 - 0 - 0 17.5 0 - 0 - 0 - 140 140 1:1 5 26 4 16 100 100 85 94 100 99 78 80 140 70 2:1 11 26 10 16 100 100 95 94 100 99 85 80 140 35 4:1 10 26 0 16 100 100 90 94 100 99 83 80 Application Rate (g/ha) PAPRH POLCO SASKR STEME VERPE VIOTR Herbicide: Compound 2-CBSU Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex 1 TEA salt Ratio 140 0 100 - 100 - 88 - 94 - 85 - 69 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 100 100 97 100 89 88 98 94 85 85 50 69 140 70 2:1 100 100 93 100 88 88 98 94 88 85 70 69 140 35 4:1 100 100 96 100 85 88 85 94 92 85 65 69 16 Table 4. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g/ha) TRZAS HORVS GALAP KCHSC LAMPU MATCH Herbicide: Compound Dichlormid Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex 1 TEA salt Ratio 140 0 26 - 16 - 100 - 94 - 99 - 80 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 15 26 20 16 100 100 100 94 100 99 73 80 140 70 2:1 6 26 15 16 100 100 85 94 100 99 84 80 140 35 4:1 7 26 0 16 100 100 83 94 100 99 73 80 Application Rate (g/ha) PAPRH POLCO SASKR STEME VERPE VIOTR Compound Herbicide: Compoundt Dichlormid Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex 1 TEA salt Ratio 140 0 100 - 100 - 88 - 94 - 85 - 69 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 100 100 98 100 90 88 98 94 90 85 68 69 140 70 2:1 100 100 99 100 80 84 90 94 93 85 65 69 140 35 4:1 100 100 98 100 95 85 95 94 90 85 48 69 17 Table 5. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g/ha) TRZAS HORVS GALAP KCHSC LAMPU MATCH Herbicide: Compound 1 Dicyclonon Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex TEA salt Ratio 140 0 26 - 16 - 100 - 94 - 99 80 0 140 0 - 0 - 0 - - 0 70 0 - 0 - 0 0 35 0 - 0 - 0 - 0 17.5 0 - 0 - 0 - 140 140 1:1 9 26 4 16 100 100 99 94 100 99 85 80 140 70 2:1 4 26 8 16 100 100 80 94 100 99 83 80 140 35 4:1 0 26 0 16 100 100 80 94 100 99 75 80 Application Rate (gfha) PAPRH POLCO SASKR STEME VERPE VIOTR Compound 1 Herbicide: Cmu 1alt Dicyclonon Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex TEA salt Ratio 140 0 100 - 100 - 88 - 94 - 85 - 69 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 0 - 0 - 0 - 0 - 0 0 35 0 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 100 100 99 100 85 88 79 94 87 85 70 69 140 70 2:1 100 100 100 100 88 88 99 94 88 85 70 69 140 35 4:1 100 100 99 100 86 88 100 94 85 85 50 69 18 Table 6. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g/ha) TRZAS HORVS GALAP KCHSC LAMPU MATCH Compound Fenchiorazole Herbicide: Compoundt Fehl o Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ratio 140 0 26 - 16 - 100 - 94 - 99 - 80 0 140 0 - 0 - 0 - - - 0 70 0 - 0 - 0 - 0 35 0 - 0 - 0 - 0 17.5 0 - 0 - 0 - - 140 140 1:1 0 26 0 16 100 100 98 94 100 99 65 80 140 70 2:1 0 26 0 16 100 100 99 94 100 99 68 80 140 35 4:1 0 26 0 16 100 100 94 94 100 99 78 80 Application Rate (g/ha) PAPRH POLCO SASKR STEME VERPE VIOTR Compound Fenchlorazole Herbicide: TEA sald Feh le Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ratio 140 0 100 - 100 - 88 - 94 - 85 - 69 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 100 100 99 100 88 88 99 94 88 85 73 69 140 70 2:1 100 100 94 100 89 88 98 94 88 85 75 69 140 35 4:1 100 100 83 100 88 88 80 94 89 85 75 69 19 Table 7. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g/ha) TRZAS HORVS GALAP KCHSC LAMPU MATCH Herbicide: Compound 1 Fenclorim Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex TEA salt Ratio 140 0 26 - 16 - 100 - 94 - 99 - 80 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 6 26 4 16 100 100 95 94 100 99 78 80 140 70 2:1 7 26 8 16 100 100 93 94 100 99 77 80 140 35 4:1 8 26 5 16 100 100 89 94 100 99 60 80 Application Rate (g/ha) PAPRH POLCO SASKR STEME VERPE VIOTR Herbicide: Compound 1 Fenclorim Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex TEA salt Ratio 140 0 100 - 100 - 88 - 94 - 85 - 69 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 100 100 99 100 85 88 94 94 93 85 65 69 140 70 2:1 100 100 99 100 89 88 88 94 90 85 68 69 140 35 4:1 100 100 96 100 88 88 93 94 90 85 65 69 20 Table 8. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g/ha) TRZAS HORVS GALAP KCHSC LAMPU MATCH Herbicide: Compound 1 Fluxofenim Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex TEA salt Ratio 140 0 26 - 16 - 100 - 94 - 99 - 80 0 140 0 - 0 - 0 - - 0 70 0 - 0 - 0 - - 0 35 0 - 0 - 0 - - 0 17.5 0 - 0 - 0 - 140 140 1:1 0 26 11 16 100 100 89 94 98 99 80 80 140 70 2:1 1 26 13 16 100 100 89 94 100 99 78 80 140 35 4:1 0 26 0 16 100 100 90 94 100 99 84 80 Application Rate (g/ha) PAPRH POLCO SASKR STEME VERPE VIOTR Herbicide: Compound 1 Fluxofenim Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex TEA salt Ratio 140 0 100 - 100 - 88 - 94 - 85 - 69 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 100 100 100 100 89 88 99 94 89 85 68 69 140 70 2:1 100 100 93 100 89 88 100 94 92 85 68 69 140 35 4:1 100 100 100 100 89 88 100 94 89 85 68 69 21 Table 9. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g/ha) TRZAS HORVS GALAP KCHSC LAMPU MATCH Compound Furilazole Herbicide: Compount (MON Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex 1 TEA salt 13900) Ratio 140 0 26 16 100 94 99 80 0 140 0 0 0 0 0 0 0 70 0 0 0 0 0 0 0 35 0 0 0 0 0 0 0 17.5 0 0 0 0 0 0 140 140 1:1 6 26 4 16 100 100 86 94 100 99 70 80 140 70 2:1 8 26 9 16 100 100 89 94 100 99 93 80 140 35 4:1 5 26 7 16 100 100 87 94 100 99 85 80 140 17.5 8:1 2 26 13 16 100 100 85 94 100 99 80 Application Rate (g/ha) PAPRH POLCO SASKR STEME VERPE VIOTR Compound Furilazole Herbicide: Compoundt (MON Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex 1 TEA salt 13900) Ratio 140 0 100 100 88 94 85 69 0 140 0 0 0 0 0 0 0 70 0 0 0 0 0 0 0 35 0 0 0 0 0 0 0 17.5 0 0 0 0 0 0 140 140 1:1 100 100 94 100 92 88 85 94 78 85 73 69 140 70 2:1 100 100 97 100 90 88 90 94 82 85 73 69 140 35 4:1 100 100 93 100 91 88 83 94 83 85 73 69 140 17.5 8:1 100 100 95 100 90 88 83 94 80 85 75 69 22 Table 10. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g/ha) TRZAS HORVS GALAP KCHSC LAMPU MATCH Herbicide: Compound 1 Mefenpyr- Safencr Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex TEA salt diethyl Ratio 140 0 26 - 16 - 100 - 94 99 - 80 0 140 0 - 0 - 0 - - 0 70 0 - 0 - 0 - 0 35 0 - 0 - 0 - 0 17.5 0 - 0 - 0 - 140 140 1:1 1 26 3 16 100 100 75 94 100 99 70 80 140 70 2:1 0 26 3 16 100 100 75 94 100 99 85 80 140 35 4:1 2 26 4 16 100 100 70 94 100 99 80 80 Application Rate (g/ha) PAPRH POLCO SASKR STEME VERPE VIOTR Herbicide: Compound 1 Mefenpyr- Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex TEA salt diethyl Ratio 140 0 100 - 100 - 88 - 94 - 85 - 69 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 100 100 98 100 94 88 87 94 88 85 75 69 140 70 2:1 100 100 95 100 90 88 88 94 88 85 75 69 140 35 4:1 100 100 90 100 88 88 88 94 83 85 70 69 23 Table 11. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g/ha) TRZAS HORVS GALAP KCHSC LAMPU MATCH d Naphthalic Herbicide: Compound aphaic Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex 1 TEA salt anhydride Ratio 140 0 26 - 16 - 100 - 94 - 99 - 80 0 140 0 - 0 - 0 - 0 70 0 - 0 - 0 - 0 35 0 - 0 - 0 - 0 17.5 0 - 0 - 0 - 140 140 1:1 13 26 8 16 100 100 91 94 100 99 93 80 140 70 2:1 16 26 11 16 100 100 93 94 100 99 87 80 140 35 4:1 10 26 4 16 100 100 94 94 100 99 75 80 Application Rate (g/ha) PAPRH POLCO SASKR STEME VERPE VIOTR Naphthalic Herbicide: Compound ahthahe Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex 1 TEA salt anhydride Ratio 140 0 100 - 100 - 88 - 94 - 85 - 69 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 100 100 99 100 88 88 94 94 87 85 78 69 140 70 2:1 100 100 100 100 89 88 95 94 85 85 75 69 140 35 4:1 100 100 98 100 87 88 98 94 88 85 70 69 24 Table 12. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g/ha) TRZAS HORVS GALAP KCHSC LAMPU MATCH Compound 1 Herbicide: Cmu 1alt Oxahetrinil Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex TEA salt Ratio 140 0 26 - 16 - 100 - 94 - 99 - 80 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 20 26 16 16 100 100 92 94 100 99 93 80 140 70 2:1 21 26 18 16 100 100 90 94 100 99 87 80 140 35 4:1 13 26 10 16 100 100 99 94 100 99 97 80 Application Rate (g/ha) PAPRI POLCO SASKR STEME VERPE VIOTR Herbicide: Compound 1 Oxabetrinil Safener Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex Ob Ex TEA salt Ratio 140 0 100 - 100 - 88 - 94 - 85 - 69 0 140 0 - 0 - 0 - 0 - 0 - 0 0 70 0 - 0 - 0 - 0 - 0 - 0 0 35 0 - 0 - 0 - 0 - 0 - 0 0 17.5 0 - 0 - 0 - 0 - 0 - 0 140 140 1:1 100 100 98 100 94 88 100 94 92 85 73 69 140 70 2:1 100 100 97 100 90 88 100 94 89 85 80 69 140 35 4:1 100 100 97 100 89 88 89 94 88 85 73 69 Table 13. Safening Activity of Herbicidal Compositions on Wheat and Barley Application Rate (g Iha) TRZAS HORVS MATCH VIOTR Herbicide: Compound Safener 1 K salt Glyphosate Ratio Ob Ex Ob Ex Ob Ex Ob Ex 8.75 0 5 - 1.7 - 50 - 20 17.5 0 8 - 3.3 - 62 - 48 35 0 27 - 6.7 - 57 - 42 0 52.5 48 - 13 - 28 - 52 8.75 52.5 1:6 37 51 12 15 55 64 75 61 7.5 52.5 1:7 37 53 10 16 58 73 77 75 35 52.5 1:1.5 45 62 12 19 75 69 83 72 5 25 Lr) if r- W cn () l 0 00I)L1)1) nt m M cz0 c-- 00004 c~ l 0- Go) mc 0 C )C 0 V) 0 0n tne Lr) tf krI V 00 0 n 0 CiCIO 0) 0 ) -r) Ir In Lr Ir~ 1 m0 < ci -~ < U CNO ON C\ CN < C\C,0 0c r40 In - 0 In M000 03 k .N N 00 !t N N'N >N cO 0 CD cn rq In =~ fN O' F- C 0000~~ -0 CO0 C If) If) If ,.CO ~ C .
Q\ C\' C\' CN C.'C\ C\ CN \C\N X en 0-C mi 0i0 c-i - x cir cc -qC xC1Cl l 1 z~ -q rn fn 0000~ -tn CD C) 0>C in 00 in 0n Ql 000 0 C~C\ C\ C C C C\ en m00m'Am C11 C11 cl Z3 Cd ~~0000C 000 c'~--N C , If it) 0f) If 0 0 06t-00 ri) 0 C '1 0z
C
c c 0 u C s kt)- W) V 00c Nq C) N q _ %) CE 6 CC4 -n cjl Ln > > o~1 4 0 tf C)z (0) In-)Lr 0' zz Z -~ CD Cf)) C0

Claims (18)

1. A composition for protecting wheat and barley from the harmful effects of a 6 (trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide of the formula (I) NH2 hal OH N 0 hal hal OR wherein hal represents F, Cl or Br, and R represents methyl or ethyl, and its agriculturally acceptable salt, ester and amide derivatives, the composition comprising the
6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide and glyphosate. 2. The composition according to claim 1, in which the 6-(trisubstituted phenyl)-4-amino-2 pyridinecarboxylate herbicide is a 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-2 pyridinecarboxylic acid derivative or a 4-amino-3-chloro-6-(2,4-dichloro-3-methoxy-phenyl)-2 pyridinecarboxylic acid derivative, or a methyl ester thereof. 3. The composition according to claim 1 or claim 2, wherein the weight ratio of the 6 (trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide to the glyphosate is from about 1:1.5 to about 1:7. 4. The composition according to claim 3, wherein the weight ratio of the 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide to the glyphosate is from about 1:1.5 to about 1:6. 5. The composition according to claim 3, wherein the weight ratio of the 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide to the glyphosate is from about 1:6 to about 1:7. 6. The composition of claim 1, wherein the herbicide of formula (1) is 31 1001125959 NH 2 Cl N OH CI F H 3 C 0 or its methyl ester or triethylammonium salt.
7. The composition of claim 1, wherein the herbicide of formula (I) is NH 2 Cl N OCH 3 CI F H 3 C 0
8. The composition of claim 2, wherein the herbicide of formula (I) is NH 2 CI N OH CI F O H 3 C' 0 or its methyl ester or triethylammonium salt.
9. The composition of claim 2, wherein the herbicide of formula (I) is NH 2 CI SFIN OCH 3 H 3 C ' O0
10. The composition of any one of the preceding claims, wherein the glyphosate protects the wheat and barley from herbicidal damage from the 6-(trisubstituted phenyl)-4-amino-2 pyridinecarboxylate herbicide without significantly reducing herbicidal activity in one or more target weed species. 32 1001125959
11. A method of protecting wheat and barley from the harmful effects of a 6-(tri substituted phenyl)-4-amino-2-pyridinecarboxylate herbicide of the formula (I) NH2I hal OH N 0 hal hal OR 1 wherein hal represents F, Cl or Br, and R represents methyl or ethyl, and its agriculturally acceptable salt, ester and amide derivatives, the method comprising contacting the wheat and barley with, or applying to an area under cultivation, a composition comprising the 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide and glyphosate.
12. The method according to claim 11, in which the 6-(trisubstituted phenyl)-4-amino-2 pyridinecarboxylate herbicide is a 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)- 2 pyridinecarboxylic acid derivative or a 4-amino-3-chloro-6-(2,4-dichloro-3-methoxy-phenyl)- 2 pyridinecarboxylic acid derivative, or a methyl ester thereof.
13. The method according to claim 11 or 12, wherein the weight ratio of the 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide to the glyphosate from about 1:1.5 to about 1:7.
14. The method according to claim 13, wherein the weight ratio of the 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide to the glyphosate is from about 1:1.5 to about 1:6.
15. The method according to claim 13, wherein the weight ratio of the 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide to the glyphosate is from about 1:6 to about 1:7.
16. The method according to claim 11, wherein the herbicide of formula (I) is: 33 1001125959 NH 2 CI N OH CI F H 3 C' 0 or its methyl ester or triethylammonium salt.
17. The method according to claim 11, wherein the herbicide of formula (I) is NH 2 CI N OCH 3 CI F O H3C'O0
18. The method according to claim 12, wherein the herbicide of formula (I) is NH 2 CI N OH CI F O H 3 C' or its methyl ester or triethylammonium salt.
19. The method according to claim 12, wherein the herbicide of formula (I) is NH 2 CI N OCH 3 Cl F O H 3 C'0
20. The method according to any one of claims 11 to 19, wherein the wheat and barley is Triticum aestivum or Hordeum vulgare.
21. The composition according to claim 1, substantially as herein described. 34 1001125959
22. The method according to claim 11, substantially as herein described. 35
AU2015203090A 2008-11-24 2015-06-10 Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops Active AU2015203090B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2015203090A AU2015203090B2 (en) 2008-11-24 2015-06-10 Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US61/117,332 2008-11-24
AU2009316667A AU2009316667B2 (en) 2008-11-24 2009-11-18 Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops
AU2015203090A AU2015203090B2 (en) 2008-11-24 2015-06-10 Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
AU2009316667A Division AU2009316667B2 (en) 2008-11-24 2009-11-18 Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops

Publications (2)

Publication Number Publication Date
AU2015203090A1 true AU2015203090A1 (en) 2015-07-02
AU2015203090B2 AU2015203090B2 (en) 2016-06-16

Family

ID=53570245

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2015203090A Active AU2015203090B2 (en) 2008-11-24 2015-06-10 Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops

Country Status (1)

Country Link
AU (1) AU2015203090B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113582915A (en) * 2021-07-25 2021-11-02 河南师范大学 Synthesis method of 4-substituted pyridine compound

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994018836A1 (en) * 1993-02-17 1994-09-01 Schering Aktiengesellschaft Synergistic herbicidal composition on the basis of thidiazimin
PL1973881T3 (en) * 2006-01-13 2010-04-30 Dow Agrosciences Llc 6-(poly-substituted aryl)-4-aminopicolinates and their use as herbicides

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113582915A (en) * 2021-07-25 2021-11-02 河南师范大学 Synthesis method of 4-substituted pyridine compound
CN113582915B (en) * 2021-07-25 2024-03-08 河南师范大学 Synthesis method of 4-substituted pyridine compound

Also Published As

Publication number Publication date
AU2015203090B2 (en) 2016-06-16

Similar Documents

Publication Publication Date Title
AU2009316667B2 (en) Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops
AU2009316671B2 (en) Safening composition of 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicides and cloquintocet-mexyl for cereal crops
US8916498B2 (en) Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on direct seeded and transplanted paddy rice
AU2016235037B2 (en) Safening of 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylic acid and derivatives thereof on cereal crops
AU2015203090B2 (en) Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops

Legal Events

Date Code Title Description
FGA Letters patent sealed or granted (standard patent)
HB Alteration of name in register

Owner name: CORTEVA AGRISCIENCE LLC

Free format text: FORMER NAME(S): DOW AGROSCIENCES, LLC