USH1711H - Herbicidal mixtures - Google Patents
Herbicidal mixtures Download PDFInfo
- Publication number
- USH1711H USH1711H US08/794,581 US79458197A USH1711H US H1711 H USH1711 H US H1711H US 79458197 A US79458197 A US 79458197A US H1711 H USH1711 H US H1711H
- Authority
- US
- United States
- Prior art keywords
- formula
- compound
- mixtures
- pat
- amino
- 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.)
- Abandoned
Links
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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
Definitions
- the present invention relates to mixtures of herbicides that have a synergistic effect on weeds.
- Combinations of herbicides are typically used to broaden the spectrum of plant control or enhance the level of control of any given species through additive effect. Certain rare combinations surprisingly give a greater-than-additive or synergistic effect. Such a valuable combination has now been discovered.
- WO 94/09629 discloses mixtures of sulfonylureas and triazolinones, but does not disclose the mixtures of this invention.
- U.S. Pat. Nos. 4,547,215 and 4,818,275 disclose Formula I compounds and the Formula II compound, respectively, but do not disclose the mixtures of this invention.
- This invention relates to mixtures of the sulfonylurea of Formula I ##STR1## (ethyl 2- (4-chloro-6-methoxy-2-pyrimidinyl)amino!carbonyl!amino!sulfonyl!benzoate, chlorimuron ethyl) and agriculturally suitable salts thereof with the triazolinone of Formula II ##STR2## (N- 2,4-dichloro-5- 4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl!phenyl!methanesulfonamide, sulfentrazone), which have now been discovered to synergistically control weeds.
- This invention also relates to herbicidal compositions comprising effective amounts of the aforesaid mixtures and at least one of the following: surfactant, solid or liquid diluent.
- This invention also relates to a method for controlling undesired vegetation comprising applying to the locus of the vegetation herbicidally effective amounts of the aforesaid mixtures.
- the preferred crop for application of the mixtures of this invention is soybean.
- the Formula I compound is prepared as described in U.S. Pat. No. 4,547,215.
- the synthesis involves the reaction of the sulfonyl isocyanate of Formula 1 with the heterocyclic amine of Formula 2. ##STR3##
- the mixtures of the present invention can include the sulfonylurea of Formula I as one or more of its agriculturally suitable salts.
- These can be prepared in a number of ways known in the art.
- metal salts can be made by contacting the sulfonylurea of Formula I with a solution of an alkali or alkaline earth metal salt having a sufficiently basic anion (e.g., hydroxide, alkoxide, carbonate or hydride).
- Quaternary amine salts can be made by similar techniques.
- Salts of the sulfonyl urea of Formula I can also be prepared by exchange of one cation for another.
- Cationic exchange can be effected by direct contact of an aqueous solution of a salt of the sulfonylurea of Formula I (e.g., alkali or quaternary amine salt) with a solution containing the cation to be exchanged. This method is most effective when the desired salt containing the exchanged cation is insoluble in water and can be separated by filtration.
- Exchange may also be effected by passing an aqueous solution of a salt of the sulfonylurea of Formula I (e.g., an alkali metal or quaternary amine salt) through a column packed with a cation-exchange resin containing the cation to be exchanged for that of the original salt and the desired product is eluted from the column.
- a salt of the sulfonylurea of Formula I e.g., an alkali metal or quaternary amine salt
- a cation-exchange resin containing the cation to be exchanged for that of the original salt and the desired product is eluted from the column.
- the Formula II triazolinone can be prepared by methods described in U.S. Pat. No. 4,818,275 which involve the reaction of the aniline of Formula 3 with methanesulfonyl chloride (Formula 4) in the presence of a base like triethylamine in a solvent like dichloromethane. ##STR4## Formulation/Utility
- the Formula I and Formula II compounds can be formulated separately and applied separately or applied simultaneously in an appropriate weight ratio, e.g., as a tank mix; or
- Mixtures of the Formula I and Formula II compounds will generally be used as a formulation with an agriculturally suitable carrier comprising a liquid or solid diluent and/or a surfactant wherein the formulation is consistent with the physical properties of the active ingredients, mode of application and environmental factors such as soil type, moisture and temperature.
- Useful formulations include liquids such as solutions (including emulsifiable concentrates), suspensions, emulsions (including microemulsions and/or suspoemulsions) and the like which optionally can be thickened into gels.
- Useful formulations further include solids such as dusts, powders, granules, pellets, tablets, films, and the like which can be water-dispersible (“wettable”) or water-soluble.
- Active ingredients can be (micro)encapsulated and further formed into a suspension or solid formulation; alternatively the entire formulation of active ingredient can be encapsulated (or "overcoated”). Encapsulation can control or delay release of the active ingredients.
- Sprayable formulations can be extended in suitable media and used at spray volumes from about one to several hundred liters per hectare. High-strength compositions are primarily used as intermediates for further formulation.
- the formulations will typically contain effective amounts of active ingredients, diluent and surfactant within the following approximate ranges which add up to 100 percent by weight.
- Typical solid diluents are described in Watkins; et al., Handbook of Insecticide Dust Diluents and Carriers, 2nd Ed., Dorland Books, Caldwell, N.J.
- Typical liquid diluents are described in Marsden, Solvents Guide, 2nd Ed., Interscience, New York, 1950. McCutcheon's Detergents and Emulsifiers Annual, Allured Publ. Corp., Ridgewood, N.J., as well as Sisely and Wood, Encyclopedia of Surface Active Agents, Chemical Publ. Co., Inc., New York, 1964, list surfactants and recommended uses. All formulations can contain minor amounts of additives to reduce foam, caking, corrosion, microbiological growth and the like, or thickeners to increase viscosity.
- Solid diluents include, for example, clays such as bentonite, montmorillinite, attapulgite and kaolin, starch, sugar, silica, talc, diatomaceous earth, urea, calcium carbonate, sodium carbonate and bicarboixate, and sodium sulfate.
- Granules and pellets can be prepared by spraying the active material upon preformed granular carders or by agglomeration techniques. See Browning, "Agglomeration", Chemical Engineering, Dec. 4, 1967, pp 147-48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York; 1963, pages 8-57 and following, and WO 91/13546; Pellets can be prepared as described in U.S. Pat. No. 4,172,714. Water-dispersible and water-soluble granules can be prepared as taught in U.S. Pat. No. 4,144,050, U.S. Pat. No. 3,920,442 and DE 3,246,493. Tablets can be prepared as taught in U.S. Pat. No.
- Test results indicate that mixture of compounds of Formula I and Formula II are highly active herbicides, providing unexpected synergistic control of selected grass and broadleaf weeds.
- the mixtures are valued, because they retain acceptable levels of crop selectivity in certain agronomic crops such as soybean and corn.
- the mixtures are particularly valued because of acceptable level of crop selectivity they retain in soybeans.
- the Formula I and Formula II mixtures of this invention can additionally be used in combination with other commercial herbicides, insecticides or fungicides.
- a mixture of one or more additional herbicides with the Formula I and Formula II mixtures of this invention may be particularly useful for weed Control.
- herbicides as mixture partners are: acetochlor, acifluoren, alachlor, atrazine, benazolin, bentazon, butylate, methyl 2-chloro-4-fluoro-5- (5,6,7,8-tetrahydro-3-oxo-1H,3H- 1,3,4!thiadiazolo3,4-a!pyridazin-1-ylidene)amino!phenyl!thio!acetate, clethodim, clomazone, clopyralid, cloransulam-methyl, cyanazine, 2,4-D, 2,4-DB, dicamba, ⁇ ,2-dichloro-5- 4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl!4-fluorobenzenepropanoate, 2- 4,5-dihydro-4-methyl-4-(1-methylethyl)-5-ox
- a herbicidally effective amount of both compounds of Formula I and Formula II will vary depending on the specific compounds selected, environmental conditions, formulation, method of application, amount and type of vegetation present, etc.
- the use ratios of Formula I and Formula II are in general 1:20 to 1:75, with ratios of 1:25 to 1:60 preferred for most uses.
- a ratio of 1:50 is particularly preferred.
- the herbicidally effective amount of the Formula I compound is a rate from 0.0005 to 1 kg ai/ha
- the herbicidally effective amount of the Formula II compound is a rate from 0.001 to 2 kg ai/ha.
- the herbicidally effective amount of the Formula I compound is a rate from 0.001 to 0.5 kg ai/ha
- herbicidally effective amount of the Formula II compound is a rate of 0.01 to 1 kg ai/ha.
- One skilled in the art can readily determine application rates and ratios of the herbicide of Formula I to the herbicide of Formula II as well as timing necessary for the desired level of weed control and crop safety.
- Soybeans (Glycine max, GLXMA), corn (Zea mays, ZEAMX), cocklebur (Xanthium strumarium, XANTH), and velvetfleaf (Abutilon theophrasti, ABUTH) were planted in 20-cm diameter pots which contained a sandy loam soil with 1.4% organic matter or silt loam soil with 3.5% organic matter.
- Compound 1 was formulated as a single active ingredient in 26.9% dry flowable granules
- Compound 2 was formulated as a single active ingredient in 79.6% dry flowable granules.
- Compounds I and 2 were applied preemergence to the soil surface of pots alone and as a mixture in a ratio of 1:46.7.
- Formulated herbicides of Compounds 1 and 2 were diluted in an aqueous solution to the appropriate concentration to deliver the desired use rate. Treatments were applied using a stationary laboratory circulating belt sprayer which was calibrated to deliver 280 L/ha through a single nozzle. Individual treatments were replicated three times and treatments were positioned in a greenhouse in a randomized complete block design. Natural light in the greenhouse was supplemented with artificial light to achieve a photoperiod of 14 hr.
- Colby's equation was used to calculate the expected additive herbicidal effect of the mixtures of Compound 1 and Compound 2.
- Colby's equation (Colby, S. R. "Calculating Synergistic and Antagonistic Responses of Herbicide Combinations,” Weeds, 15(1), pp 20-22 (1967)) calculates the expected additive effect of herbicidal mixtures, and for two active ingredients is of the form:
- P a is the observed percentage effect of the first active ingredient at the same use rate as in the mixture
- P b is the observed percentage effect of the second active ingredient at the same use rate as in the mixture.
- Tables 1 and 2 represent final assessment of weed control and crop injury at 21 days after treatment with Compound 1 and Compound 2 applied alone as single active ingredients, applied as a mixture of the two active ingredients of Compound 1 and Compound 2, and the expected additive effect of the herbicidal mixture of Compound 1 and Compound 2 (Colby's equation). Different ratios of Compound 1 to Compound 2, and different formulation types, also provide useful weed control from the combination of the two herbicides.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
This invention relates to herbicidal mixtures of chlorimuron ethyl and sulfentrazone, herbicidal compositions of said mixtures, and a method for the use of said mixtures to control undesired vegetation.
Description
The present invention relates to mixtures of herbicides that have a synergistic effect on weeds.
The control of undesired vegetation is extremely important in achieving high crop efficiency. This can be achieved by the selective control of the growth of weeds in such useful crops as soybean, among others. Unchecked weed growth in such useful crops can cause significant reduction in productivity and thereby result in increased costs to the consumers. The need for finding products that achieve such results continues to be commercially important.
Combinations of herbicides are typically used to broaden the spectrum of plant control or enhance the level of control of any given species through additive effect. Certain rare combinations surprisingly give a greater-than-additive or synergistic effect. Such a valuable combination has now been discovered.
WO 94/09629 discloses mixtures of sulfonylureas and triazolinones, but does not disclose the mixtures of this invention. U.S. Pat. Nos. 4,547,215 and 4,818,275 disclose Formula I compounds and the Formula II compound, respectively, but do not disclose the mixtures of this invention.
This invention relates to mixtures of the sulfonylurea of Formula I ##STR1## (ethyl 2- (4-chloro-6-methoxy-2-pyrimidinyl)amino!carbonyl!amino!sulfonyl!benzoate, chlorimuron ethyl) and agriculturally suitable salts thereof with the triazolinone of Formula II ##STR2## (N- 2,4-dichloro-5- 4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl!phenyl!methanesulfonamide, sulfentrazone), which have now been discovered to synergistically control weeds. This invention also relates to herbicidal compositions comprising effective amounts of the aforesaid mixtures and at least one of the following: surfactant, solid or liquid diluent. This invention also relates to a method for controlling undesired vegetation comprising applying to the locus of the vegetation herbicidally effective amounts of the aforesaid mixtures.
For reason of weed control spectrum and/or crop selectivity, the preferred crop for application of the mixtures of this invention is soybean.
The Formula I compound is prepared as described in U.S. Pat. No. 4,547,215. The synthesis involves the reaction of the sulfonyl isocyanate of Formula 1 with the heterocyclic amine of Formula 2. ##STR3##
The mixtures of the present invention can include the sulfonylurea of Formula I as one or more of its agriculturally suitable salts. These can be prepared in a number of ways known in the art. For example, metal salts can be made by contacting the sulfonylurea of Formula I with a solution of an alkali or alkaline earth metal salt having a sufficiently basic anion (e.g., hydroxide, alkoxide, carbonate or hydride). Quaternary amine salts can be made by similar techniques.
Salts of the sulfonyl urea of Formula I can also be prepared by exchange of one cation for another. Cationic exchange can be effected by direct contact of an aqueous solution of a salt of the sulfonylurea of Formula I (e.g., alkali or quaternary amine salt) with a solution containing the cation to be exchanged. This method is most effective when the desired salt containing the exchanged cation is insoluble in water and can be separated by filtration.
Exchange may also be effected by passing an aqueous solution of a salt of the sulfonylurea of Formula I (e.g., an alkali metal or quaternary amine salt) through a column packed with a cation-exchange resin containing the cation to be exchanged for that of the original salt and the desired product is eluted from the column. This method is particularly useful when the desired salt is water soluble (e.g., a potassium, sodium or calcium salt).
The Formula II triazolinone can be prepared by methods described in U.S. Pat. No. 4,818,275 which involve the reaction of the aniline of Formula 3 with methanesulfonyl chloride (Formula 4) in the presence of a base like triethylamine in a solvent like dichloromethane. ##STR4## Formulation/Utility
The mixtures of the Formula I and Formula II compounds can be formulated in a number of ways:
(a) the Formula I and Formula II compounds can be formulated separately and applied separately or applied simultaneously in an appropriate weight ratio, e.g., as a tank mix; or
(b) the Formula I and Formula II compounds can be formulated together in the proper weight ratio.
Mixtures of the Formula I and Formula II compounds will generally be used as a formulation with an agriculturally suitable carrier comprising a liquid or solid diluent and/or a surfactant wherein the formulation is consistent with the physical properties of the active ingredients, mode of application and environmental factors such as soil type, moisture and temperature. Useful formulations include liquids such as solutions (including emulsifiable concentrates), suspensions, emulsions (including microemulsions and/or suspoemulsions) and the like which optionally can be thickened into gels. Useful formulations further include solids such as dusts, powders, granules, pellets, tablets, films, and the like which can be water-dispersible ("wettable") or water-soluble. Active ingredients can be (micro)encapsulated and further formed into a suspension or solid formulation; alternatively the entire formulation of active ingredient can be encapsulated (or "overcoated"). Encapsulation can control or delay release of the active ingredients. Sprayable formulations can be extended in suitable media and used at spray volumes from about one to several hundred liters per hectare. High-strength compositions are primarily used as intermediates for further formulation.
The formulations will typically contain effective amounts of active ingredients, diluent and surfactant within the following approximate ranges which add up to 100 percent by weight.
______________________________________
Weight Percent
Active
Ingredient
Diluent Surfactant
______________________________________
Water-Dispersible and
5-90 0-94 1-15
Water-soluble
Granules, Tablets and Powders.
Suspensions, Emulsions,
5-50 40-95 0-15
Solutions
(including Emulsifiable
Concentrates)
Dusts 1-25 70-99 0-5
Granules and Pellets
0.01-99 5-99.99
0-15
High Strength Compositions
90-99 0-10 0-2
______________________________________
Typical solid diluents are described in Watkins; et al., Handbook of Insecticide Dust Diluents and Carriers, 2nd Ed., Dorland Books, Caldwell, N.J. Typical liquid diluents are described in Marsden, Solvents Guide, 2nd Ed., Interscience, New York, 1950. McCutcheon's Detergents and Emulsifiers Annual, Allured Publ. Corp., Ridgewood, N.J., as well as Sisely and Wood, Encyclopedia of Surface Active Agents, Chemical Publ. Co., Inc., New York, 1964, list surfactants and recommended uses. All formulations can contain minor amounts of additives to reduce foam, caking, corrosion, microbiological growth and the like, or thickeners to increase viscosity.
Surfactants include, for example, polyethoxylated alcohols, polyethoxylated alkylphenols, polyethoxylated sorbitan fatty acid esters, dialkyl sulfosuccinates, alkyl sulfates, alkylbenzene sulfonates, organosilicones, N,N-dialkyltaurates, lignin sulfonates, naphthalene sulfonate formaldehyde condensates, polycarboxylates, and polyoxyethylene/polyoxypropylene block copolymers. Solid diluents include, for example, clays such as bentonite, montmorillinite, attapulgite and kaolin, starch, sugar, silica, talc, diatomaceous earth, urea, calcium carbonate, sodium carbonate and bicarboixate, and sodium sulfate. Liquid diluents include, for example, water, N,N-dimethylformamide, dimethyl sulfoxide, N-alkylpyrrolidone, ethylene glycol, polypropylene glycol, paraffins, alkylbenzenes, alkylnaphthalenes, oils of olive, castor, linseed, tung, sesame, corn, peanut, cotton-seed, soybean, rape-seed and coconut, fatty acid esters, ketones such as cyclohexanone, 2-heptanone, isophorone and 4-hydroxy-4-methyl-2-pentanone, alcohols such as methanol, cyclohexanol, decanol and tetrahydrofurfuryl alcohol.
Solutions, including emulsifiable concentrates, can be prepared by simply mixing the ingredients. Chemically stabilized aqueous sulfonylurea or agriculturally suitable sulfonylurea salt dispersions are taught in U.S. Pat. No. 4,936,900. Solution formulations of sulfonylureas with improved chemical stability are taught in U.S. Pat. No. 4,599,412. Dusts and powders can be prepared by blending and, usually, grinding as in a hammer mill or fluid-energy mill. Suspensions are usually prepared by wet-milling; see, for example, U.S. Pat. No. 3,060,084. Granules and pellets can be prepared by spraying the active material upon preformed granular carders or by agglomeration techniques. See Browning, "Agglomeration", Chemical Engineering, Dec. 4, 1967, pp 147-48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York; 1963, pages 8-57 and following, and WO 91/13546; Pellets can be prepared as described in U.S. Pat. No. 4,172,714. Water-dispersible and water-soluble granules can be prepared as taught in U.S. Pat. No. 4,144,050, U.S. Pat. No. 3,920,442 and DE 3,246,493. Tablets can be prepared as taught in U.S. Pat. No. 5,180,587, U.S. Pat. No. 5,232,701 and U.S. Pat. No. 5,208,030. Fills can be prepared as taught in GB 2,095,558 and U.S. Pat. No. 3,299,566.
For further information regarding formulation, see U.S. Pat. No. 3,235,361, Col. 6, line 16 through Col. 7, line 19 and Examples 10-41; U.S. Pat. No. 3,309,192, Col. 5, line 43 through Col. 7, line 62 and Examples 8, 12, 15, 39, 41, 52, 53, 58, 132, 138-140, 162-164, 166, 167 and 169-182; U.S. Pat. No. 2,891,855, Col. 3, line 66 through Col. 5, line 17 and Examples 1-4; Klingman, Weed Control as a Science, John Wiley and Sons, Inc., New York, 1961, pp 81-96; and Hance et al., Weed Control Handbook, 8th Ed., Blackwell Scientific Publications, Oxford, 1989.
In the following Examples, all percentages are by weight and all formulations are prepared in conventional ways. Compound numbers refer to compounds identified on Page 8.
______________________________________
High Strength Concentrate
______________________________________
Compound 1 4.7%
Compound 2 93.8%
silica aerogel 0.5%
synthetic amorphous fine silica
1.0%.
______________________________________
______________________________________
Wettable Powder
______________________________________
Compound 1 0.9%
Compound 2 64.1%
dodecylphenol polyethylene glycol ether
2.0%
sodium ligninsulfonate
4.0%
sodium silicoaluminate
6.0%
montmorillonite (calcined)
23.0%.
______________________________________
______________________________________
Granule
______________________________________
Compound 1 0.4%
Compound 2 9.6%
attapulgite granules (low volatile matter,
90.0%.
0.71/0.30 mm; U.S.S. No. 25-50 sieves)
______________________________________
______________________________________
Aqueous Suspension
______________________________________
Compound 1 0.4%
Compound 2 24.6%
hydrated attapulgite
3.0%
crude calcium ligninsulfonate
10.0%
sodium dihydrogen phosphate
0.5%
water 61.5%.
______________________________________
______________________________________
Extruded Pellet
______________________________________
Compound 1 0.5%
Compound 2 24.5%
anhydrous sodium sulfate
10.0%
crude calcium ligninsulfonate
5.0%
sodium alkylnaphthalenesulfonate
1.0%
calcium/magnesium bentonite
59.0%.
______________________________________
Test results indicate that mixture of compounds of Formula I and Formula II are highly active herbicides, providing unexpected synergistic control of selected grass and broadleaf weeds. The mixtures are valued, because they retain acceptable levels of crop selectivity in certain agronomic crops such as soybean and corn. The mixtures are particularly valued because of acceptable level of crop selectivity they retain in soybeans.
The Formula I and Formula II mixtures of this invention can additionally be used in combination with other commercial herbicides, insecticides or fungicides. A mixture of one or more additional herbicides with the Formula I and Formula II mixtures of this invention may be particularly useful for weed Control. Examples of other herbicides as mixture partners are: acetochlor, acifluoren, alachlor, atrazine, benazolin, bentazon, butylate, methyl 2-chloro-4-fluoro-5- (5,6,7,8-tetrahydro-3-oxo-1H,3H- 1,3,4!thiadiazolo3,4-a!pyridazin-1-ylidene)amino!phenyl!thio!acetate, clethodim, clomazone, clopyralid, cloransulam-methyl, cyanazine, 2,4-D, 2,4-DB, dicamba, α,2-dichloro-5- 4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl!4-fluorobenzenepropanoate, 2- 4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl!-5-(methoxylmethyl)-3-pyridinecarboxylic acid, dimethenamid, EPTC, ethalfluralin, fenoxaprop, fluazifop, fluazifop-P, flumetsulam, fluminclorac pentyl ester, flumioxazin, fomesafen, glufosinate, glyphosate, halosulfuron, haloxyfop, imazaquin, imazethapyr, isoxaflutole, lactofen, linuron, MCPA, N- (4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino!carbonyl!-2-(3,3,3-trifluoropropyl)benzenesulfonamide, metolachlor, metribuzin, mefluidide, nicosulfuron, 3-oxetanyl 2- (4,6-dimethyl-2-pyrimidinyl)amino!carbonyl!amino!sulfonyl!benzoate, paraquat, pendimethalin, primisulfuron, pyridate, quizalofop-ethyl, quizalofop-P-ethyl, sethoxydim, simazine, sulcotdone, thiafluamide, thiensulfuron, tridiphane, trifluralin, vernolate.
A herbicidally effective amount of both compounds of Formula I and Formula II will vary depending on the specific compounds selected, environmental conditions, formulation, method of application, amount and type of vegetation present, etc. The use ratios of Formula I and Formula II are in general 1:20 to 1:75, with ratios of 1:25 to 1:60 preferred for most uses. A ratio of 1:50 is particularly preferred. In general, the herbicidally effective amount of the Formula I compound is a rate from 0.0005 to 1 kg ai/ha, and the herbicidally effective amount of the Formula II compound is a rate from 0.001 to 2 kg ai/ha. Preferably, the herbicidally effective amount of the Formula I compound is a rate from 0.001 to 0.5 kg ai/ha, and herbicidally effective amount of the Formula II compound is a rate of 0.01 to 1 kg ai/ha. One skilled in the art can readily determine application rates and ratios of the herbicide of Formula I to the herbicide of Formula II as well as timing necessary for the desired level of weed control and crop safety.
The following Formula I sulfonylurea (Compound 1) was tested in combination with the Formula II triazolinone (Compound 2). ##STR5##
The following test protocol was used for the tests in Tables 1 and 2. The data demonstrate the efficacy of the Formula I and Formula II mixtures of this invention against specific weeds. The weed control afforded by the mixtures of this invention are not limited, however, to these species.
Test Protocol
Soybeans (Glycine max, GLXMA), corn (Zea mays, ZEAMX), cocklebur (Xanthium strumarium, XANTH), and velvetfleaf (Abutilon theophrasti, ABUTH) were planted in 20-cm diameter pots which contained a sandy loam soil with 1.4% organic matter or silt loam soil with 3.5% organic matter. Compound 1 was formulated as a single active ingredient in 26.9% dry flowable granules, and Compound 2 was formulated as a single active ingredient in 79.6% dry flowable granules. Compounds I and 2 were applied preemergence to the soil surface of pots alone and as a mixture in a ratio of 1:46.7. Formulated herbicides of Compounds 1 and 2 were diluted in an aqueous solution to the appropriate concentration to deliver the desired use rate. Treatments were applied using a stationary laboratory circulating belt sprayer which was calibrated to deliver 280 L/ha through a single nozzle. Individual treatments were replicated three times and treatments were positioned in a greenhouse in a randomized complete block design. Natural light in the greenhouse was supplemented with artificial light to achieve a photoperiod of 14 hr.
Assessments of weed control and crop injury were made by visually evaluating plants at 21 days after treatment. Visual rating was made using a 0 to 100% scale where 0% represents no difference relative to an untreated control and 100% represents complete kill of the given crop or weed species.
Colby's equation was used to calculate the expected additive herbicidal effect of the mixtures of Compound 1 and Compound 2. Colby's equation (Colby, S. R. "Calculating Synergistic and Antagonistic Responses of Herbicide Combinations," Weeds, 15(1), pp 20-22 (1967)) calculates the expected additive effect of herbicidal mixtures, and for two active ingredients is of the form:
P.sub.a+b =P.sub.a +P.sub.b -(P.sub.a P.sub.b /100)
wherein Pa+b is the percentage effect of the mixture expected from additive contribution of the individual components,
Pa is the observed percentage effect of the first active ingredient at the same use rate as in the mixture, and
Pb is the observed percentage effect of the second active ingredient at the same use rate as in the mixture.
Tables 1 and 2 represent final assessment of weed control and crop injury at 21 days after treatment with Compound 1 and Compound 2 applied alone as single active ingredients, applied as a mixture of the two active ingredients of Compound 1 and Compound 2, and the expected additive effect of the herbicidal mixture of Compound 1 and Compound 2 (Colby's equation). Different ratios of Compound 1 to Compound 2, and different formulation types, also provide useful weed control from the combination of the two herbicides.
TABLE 1
______________________________________
Effect of Compound 1 and Comound 2 as active ingredients alone
and in a mixture on Glycine max (GLXMA), Zea mays (ZEAMX),
Xanthium strumarium (XANTH), and Abutilon theophrasti (ABUTH)
in a sandy loam soil containing 1.4% organic matter.
Evaluation 21 days after treatment
Com- % Injury % Control
pound Rate (g ai/ha)
GLXMA ZEAMX XANTH ABUTH
______________________________________
1 0.19 0 30 15 30
0.28 0 47 0 40
0.38 0 30 7 30
0.56 0 40 20 27
0.75 0 47 20 40
1.5 3 57 67 57
2 8.8 0 0 0 0
13.1 0 0 0 3
17.5 0 3 0 10
26.2 0 0 0 7
35 0 10 5 10
70 0 13 35 37
1 + 2 0.19 ± 8.8
0 (0)* 27 (30)
3 (15)
17 (30)
0.28 + 13.1
0 (0) 27 (47)
20 (0) 37 (42)
0.38 + 17.5
0 (0) 30 (32)
10 (7) 40 (37)
0.56 + 26.2
5 (0) 47 (40)
33 (20)
73 (32)
0.75 + 35 3 (0) 50 (52)
50 (24)
73 (46)
1.5 + 70 7 (3) 53 (63)
97 (79)
87 (73)
______________________________________
*Expected effects in parentheses are calculated according to Colby, S. R.
"Calculating Synergistic and Antagonistic Responses of Herbicide
Combination, " Weeds, 15 (1), pp 20-22 (1967).
TABLE 2
______________________________________
Effect of Compound 1 and Comound 2 as active ingredients alone
and in a mixture on Glycine max (GLXMA), Zea mays (ZEAMX),
Xanthium strumarium (XANTH), and Abutilon theophrasti (ABUTH)
in a silt loam soil containing 3.5% organic matter.
Evaluation 21 days after treatment
Com- % Injury % Control
pound Rate (g ai/ha)
GLXMA ZEAMX XANTH ABUTH
______________________________________
1 0.75 0 27 0 13
1.1 3 27 20 20
1.5 3 47 25 27
2.2 10 50 87 37
3 10 67 83 47
6 7 63 73 67
2 35 0 0 25 13
42.5 0 3 20 15
70 0 7 27 97
105 13 33 77 83
140 23 43 100 100
280 63 90 100 100
1 + 2 0.75 + 35 0 (0)* 20 (27)
90 (25)
67 (24)
1.1 + 42.5
10 (3) 43 (29)
80 (36)
70 (32)
1.5 + 70 0 (3) 37 (51)
8 (45)
80 (98)
2.2 + 105 13 (22) 27 (67)
77 (97)
80 (89)
3 + 140 30 (31) 47 (81)
97 (100)
93 (100)
6 + 280 77 (66) 67 (96)
100 (100)
100 (100)
______________________________________
*Expected effects in parentheses are calculated according to Colby, S. R.
"Calculating Synergistic and Antagonistic Responses of Herbicide
Combination, " Weeds, 15 (1), pp 20-22 (1967).
Claims (5)
1. A herbicidal mixture comprising the compound of Formula I ##STR6## which is ethyl 2- (4-chloro-6-methoxy-2-pyrimidinyl)amino!carbonyl!amino!sulfonyl!benzoate (chlorimuron ethyl) and agriculturally suitable salts thereof and the compound of Formula II ##STR7## which is N- 2,4-dichloro-5- 4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl!phenyl!methanesulfonamide (sulfentrazone), wherein the ratio of the compound of Formula I to the compound of Formula II is in the range of 1:20 to 1:75.
2. An agriculturally suitable composition for controlling the growth of undesired vegetation comprising an effective amount of the herbicidal mixtures of claim 1 and at least one of the following: surfactant, solid or liquid diluent.
3. The composition of claim 2 wherein the undesired vegetation is the vegetation in a soybean crop.
4. A method for controlling the growth of undesired vegetation comprising contacting the locus to be protected with a herbicidally effective amount of the composition of claim 2.
5. The method of claim 4 wherein the locus to be protected is a soybean crop.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/794,581 USH1711H (en) | 1997-02-03 | 1997-02-03 | Herbicidal mixtures |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/794,581 USH1711H (en) | 1997-02-03 | 1997-02-03 | Herbicidal mixtures |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USH1711H true USH1711H (en) | 1998-02-03 |
Family
ID=25163058
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/794,581 Abandoned USH1711H (en) | 1997-02-03 | 1997-02-03 | Herbicidal mixtures |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USH1711H (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001022819A1 (en) * | 1999-09-30 | 2001-04-05 | Bayer Aktiengesellschaft | Selective herbicides on the basis of n-aryl-triazoline(thi)ones |
| US20100016159A1 (en) * | 2006-07-19 | 2010-01-21 | Syngenta Crop Protection, Inc. | Herbicidal composition and method of use thereof |
| US20100093539A1 (en) * | 2005-08-10 | 2010-04-15 | Ishihara Sangyo Kaisha, Ltd. | Water-based herbicidal suspension of sulfonylurea |
| US8536094B2 (en) | 1998-08-13 | 2013-09-17 | Bayer Intellectual Property Gmbh | Herbicidal compositions for tolerant or resistant rice crops |
| CN103783064A (en) * | 2014-03-04 | 2014-05-14 | 山东潍坊润丰化工股份有限公司 | Weeding composition containing sulfentrazone and chlorimuron-ethyl and application thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4547215A (en) * | 1983-03-24 | 1985-10-15 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
| US4818275A (en) * | 1985-12-20 | 1989-04-04 | Fmc Corporation | Herbicidal aryl triazolinones |
-
1997
- 1997-02-03 US US08/794,581 patent/USH1711H/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4547215A (en) * | 1983-03-24 | 1985-10-15 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
| US4818275A (en) * | 1985-12-20 | 1989-04-04 | Fmc Corporation | Herbicidal aryl triazolinones |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8536094B2 (en) | 1998-08-13 | 2013-09-17 | Bayer Intellectual Property Gmbh | Herbicidal compositions for tolerant or resistant rice crops |
| WO2001022819A1 (en) * | 1999-09-30 | 2001-04-05 | Bayer Aktiengesellschaft | Selective herbicides on the basis of n-aryl-triazoline(thi)ones |
| US20100093539A1 (en) * | 2005-08-10 | 2010-04-15 | Ishihara Sangyo Kaisha, Ltd. | Water-based herbicidal suspension of sulfonylurea |
| US8501667B2 (en) * | 2005-08-10 | 2013-08-06 | Ishihara Sangyo Kaisha, Ltd. | Water-based herbicidal suspension |
| US20100016159A1 (en) * | 2006-07-19 | 2010-01-21 | Syngenta Crop Protection, Inc. | Herbicidal composition and method of use thereof |
| US8815774B2 (en) | 2006-07-19 | 2014-08-26 | Syngenta Crop Protection Llc | Herbicidal composition and method of use thereof |
| CN103783064A (en) * | 2014-03-04 | 2014-05-14 | 山东潍坊润丰化工股份有限公司 | Weeding composition containing sulfentrazone and chlorimuron-ethyl and application thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6046134A (en) | Herbicidal mixtures | |
| KR100682203B1 (en) | Herbicides with acylated aminophenylsulfonyl urea | |
| AU2002311427B2 (en) | Synergistic herbicidal compostions comprising mesotrione | |
| CZ20021377A3 (en) | Synergistic herbicidal compositions containing herbicidal agents selected fro the group of hydroxyphenylpyruvate-dioxygenase inhibitors | |
| US5696051A (en) | Synergistic herbicide combinations | |
| CZ303507B6 (en) | Combination of herbicidal agents, method of controlling harmful plants and use of such herbicidal agent combination for controlling harmful plants | |
| US5798317A (en) | Herbicidal mixtures comprising anilofos and other herbicides | |
| EP0774904B1 (en) | Herbicidal mixtures | |
| JP2006124388A (en) | New combinational agent consisting of herbicide and chemical injury mitigating agent | |
| AU2002356585B2 (en) | Syngergististic herbicides containing herbicides from the group of benzoylpyrazoles | |
| USH1711H (en) | Herbicidal mixtures | |
| EP0823837B1 (en) | Herbicidal mixtures | |
| US6114283A (en) | Herbicidal mixtures | |
| US5990045A (en) | Herbicidal mixtures | |
| US5928995A (en) | Herbicidal mixtures | |
| KR100443388B1 (en) | Herbicidal Mixtures | |
| EP1073336A1 (en) | Herbicidal mixtures | |
| EP0890311A2 (en) | Herbicidal mixtures | |
| AU737523B2 (en) | Herbicidal mixtures | |
| WO1998058545A1 (en) | Herbicidal mixtures |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCF | Information on status: patent grant |
Free format text: PATENTED CASE |