Classifications

• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
  • A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
  • A01N35/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing keto or thioketo groups as part of a ring, e.g. cyclohexanone, quinone; Derivatives thereof, e.g. ketals
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
  • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
  • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
  • A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings

Definitions

• This application claims the benefit of United States Provisional Application Serial Number 61/117,330 filed on November 24, 2008.
• This invention concerns the safening of the herbicidal injury caused by 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylates in cereal crops.
• the cultivated plants 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 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 i.e.
• 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 substances or classes of substances. It has also been found that the antidotes proposed frequently are used at rates higher than the rates of the individual herbicidal substance.
• 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 of damage to both wheat and barley at concentrations required to adequately control the undesirable vegetation. U.S. Patent 7,314,849 B2 also describes the safening of the herbicidal injury with cloquintocet-mexyl at herbicide-to-safener ratio that lies within the range of between 1: 1 and 1:4, i.e., at a ratio where the rate of safener is equal to or exceeds the rate of the herbicide. O
• the present 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)
• hal represents F, Cl or Br
• R represents methyl or ethyl
• a safener selected from the quinolinyloxyacetate family of chemicals in which the weight ratio of 6-(trisubstituted aryl)- 4-amino-2-pyridinecarboxylate herbicide to quinolinyloxyacetate safener is between 2:1 to 64:1.
• the unexpectedly low rates of quinolinyloxyacetate prevent the herbicidal effects of a 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide of the formula (I) on cereal crops such as wheat and barley.
• the present invention also concerns 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)
• hal represents F, Cl or Br
• R represents methyl or ethyl
• 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.
• the quinolinyloxyacetate safener is cloquintocet, most preferably cloquintocet-mexyl.
• the pyridinecarboxylic acids of formula I are a new class of compounds having herbicidal activity.
• a number of pyridinecarboxylic acid compounds are described in U.S. Patent 7,314,849 B2, including 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)- pyridine-2-carboxylic acid.
• the pyridinecarboxylic acids of formula (I) control annual grass weeds and broadleaf weeds in wheat and barley but can be phytotoxic to wheat and barley at commercially herbicidal doses.
• Safeners from the quinolinyloxyacetate family of chemicals are described in U.S. Patent 4,902,340.
• the preferred safeners from the quinolinyloxyacetate family of chemicals are derivatives of cloquintocet, most preferably the mexyl ester.
• Cloquintocet is the common O
• 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.
• plants and vegetation include germinant seeds, emerging seedlings and established vegetation.
• safener 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 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 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.
• Safening means preventing the adverse effect of an herbicide on the cultivated plants, i.e., protecting the cultivated plants without, at the same time, noticeably influencing the herbicidal action on weeds to be combated.
• the weight ratio of the pyridinecarboxylic acid of formula (I) to the safener at which the herbicidal effect on the cultivated plant is prevented lies within the range of between 2: 1 and 64: 1.
• the weight ratio of the pyridinecarboxylic acid of formula (I) to the safener at which the herbicidal effect on the cultivated plant is prevented lies within the range of between 4:1 and 32:1.
• 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 application.
• the composition of the invention can be applied at an application rate of between 0.8 grams per hectare (g/ha) and 350 g/ha based on the total amount of pyridinecarboxylic acid of formula (I) and safener in the composition.
• cloquintocet is applied at a rate between 0.273 g/ha and 70 g/ha and the pyridinecarboxylic acid of formula (I) component is applied at a rate between 0.55 g/ha and 280 g/ha.
• the pyridinecarboxylic acid of formula (I) and the safener of the present invention can be applied either separately or together as part of a multipart herbicidal system.
• 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.
• 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.
• 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 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.
• 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 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 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 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 -C 11 alkylpolyglycoside; phosphated alcohol ethoxylate; natural primary alcohol (Ci 2 -Ci6) 5 ethoxylate; di-seobutylphenol EO-PO block copolymer; polysiloxane-methyl cap; nonylphenol ethoxylate + urea ammonium nitrate; emulsified methylated seed oil; tridecyl alcohol (synthetic) ethoxylate (8EO); t
• Liquid carriers that can be employed include water, toluene, xylene, petroleum 10 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, N,N-dimethyl alkylamides, dimethyl sulfoxide, liquid fertilizers and the like. 15 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.
• compositions of the present invention 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
• Typical surface-active agents include salts of alkyl sulfates, such as diethanolammonium
• alkylarylsulfonate salts such as calcium dodecylbenzenesulfonate
• alky lphenol- alky lene oxide addition products such as nonylphenol-Cig ethoxylate
• alcohol- alky lene oxide addition products such as tridecyl alcohol-Ci6 ethoxylate
• soaps such O
• 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 trimethylammonium chloride
• polyethylene glycol esters of fatty acids such as polyethylene glycol stearate
• 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.
• compositions may also contain other compatible components, for example, other herbicides, 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 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 1 weight percent active ingredient and preferably contain 0.001 to 0.05 weight percent.
• 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.
• 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 ).
• a fungicide treatment and/or other chemical or 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 0 C during the day and 17 0 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 leaf stage.
• 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 experimental compound mixtures were prepared by adding the appropriate volume of both 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 2 ) at a spray height of 18 inches (43 centimeters (cm)) above average plant canopy. Control plants were sprayed in the same manner with the solvent blank.
• 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 O
• 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.).
• TRZAS Triticum aestivum (spring wheat)
• MATCH Matricaria chamomila (scented mayweed)
• TRZAW Triticum aestivum (winter wheat)
• PAPRH Papaver rhoeas (corn poppy)
• TRZDU Triticum durum (durum wheat)
• POLCO Polygonum convolvulus (wild buckwheat)
• HORVS Hordeum vulgare (spring barley)
• SASKR Salsola iberica (Russian thistle)
• HORVW Hordeum vulgare (winter barley)
• STEME Stellaria media (common chickweed)
• GALAP Galium aparine (cleavers)
• VERPE Veronica persica (bird's-eye speedwell)
• KCHSC Kochia scoparia (kochia)
• VIOTR Viola tricolor (wild pansy)
• LAMPU Lamium purpureum (purple deadnettle)
• Ob Observ

Landscapes

• Life Sciences & Earth Sciences (AREA)
• Health & Medical Sciences (AREA)
• General Health & Medical Sciences (AREA)
• Dentistry (AREA)
• Plant Pathology (AREA)
• Engineering & Computer Science (AREA)
• Agronomy & Crop Science (AREA)
• Wood Science & Technology (AREA)
• Zoology (AREA)
• Environmental Sciences (AREA)
• Pest Control & Pesticides (AREA)
• Toxicology (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Pyridine Compounds (AREA)

Priority Applications (15)

Applications Claiming Priority (2)

Publications (2)

Family

ID=42196874

Family Applications (1)

Country Status (18)

Cited By (15)

Families Citing this family (10)

Citations (3)

Family Cites Families (8)

• 2009
  • 2009-11-18 DK DK09761099.2T patent/DK2361013T3/da active
  • 2009-11-18 JP JP2011537568A patent/JP5658164B2/ja active Active
  • 2009-11-18 EA EA201100835A patent/EA019904B1/ru not_active IP Right Cessation
  • 2009-11-18 WO PCT/US2009/064926 patent/WO2010059680A2/en active Application Filing
  • 2009-11-18 EP EP09761099.2A patent/EP2361013B1/de active Active
  • 2009-11-18 CN CN200980146711.7A patent/CN102245020B/zh active Active
  • 2009-11-18 UA UAA201106496A patent/UA105907C2/uk unknown
  • 2009-11-18 BR BRPI0921191-8A patent/BRPI0921191B1/pt active IP Right Grant
  • 2009-11-18 AU AU2009316671A patent/AU2009316671B2/en active Active
  • 2009-11-18 US US12/620,905 patent/US8609586B2/en active Active
  • 2009-11-18 ES ES09761099T patent/ES2430052T3/es active Active
  • 2009-11-18 CA CA2743171A patent/CA2743171C/en active Active
  • 2009-11-18 MX MX2011005486A patent/MX2011005486A/es active IP Right Grant
  • 2009-11-18 KR KR1020117011661A patent/KR101724163B1/ko active IP Right Grant
  • 2009-11-18 PL PL09761099T patent/PL2361013T3/pl unknown
  • 2009-11-23 AR ARP090104509A patent/AR075305A1/es active IP Right Grant
• 2011
  • 2011-04-28 ZA ZA2011/03111A patent/ZA201103111B/en unknown
  • 2011-05-24 IL IL213124A patent/IL213124A/en active IP Right Grant
• 2013
  • 2013-12-12 US US14/104,651 patent/US9040458B2/en active Active
• 2014
  • 2014-11-27 JP JP2014240228A patent/JP5976081B2/ja active Active

Patent Citations (4)

Also Published As

Similar Documents

Legal Events