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06/18/09 - USPTO Class 504 |  25 views | #20090156400 | Prev - Next | About this Page  504 rss/xml feed  monitor keywords

Herbicide combinations comprising specific sulfonylureas

USPTO Application #: 20090156400
Title: Herbicide combinations comprising specific sulfonylureas
Abstract: in which R1 is (C1-C8)-alkyl, (C3-C4)-alkenyl, (C3-C4)-alkynyl, or (C1-C4)-alkyl which is mono- to tetrasubstituted by radicals selected from the group consisting of halogen and/or (C1-C2)-alkoxy, R2 is I or CH2NHSO2CH3, R3 is methyl or methoxy and Z is N or CH and (B) denotes one or more herbicides which act selectively in some monocotyledonous crops against monocotyledonous and/or dicotyledonous harmful plants, which herbicides are selected from the group of compounds consisting of flucarbazone, BAY MKH 6561 (procarbazone), florasulam, halosulfuron, tritosulfuron, picolinafen, cinidon-ethyl, mesotrione, metosulam, clopyralid, flufenacet, flumetsulam, flupoxam, prosulfocarb, flurtamone, aclonifen, hexazinone, asulam, diuron, ametryn, isoxaflutole, amicarbazone and trifloxysulfuron. Herbicide combinations comprising an effective amount of components (A) and (B) have improved herbicidal action wherein (A) is one or more herbicides of the formula (I) or salts thereof (end of abstract)



Agent: Frommer Lawrence & Haug - New York, NY, US
Inventors: Bieringer, Hans Philipp Huff, Erwin Hacker
USPTO Applicaton #: 20090156400 - Class: 504134 (USPTO)

Herbicide combinations comprising specific sulfonylureas description/claims


The Patent Description & Claims data below is from USPTO Patent Application 20090156400, Herbicide combinations comprising specific sulfonylureas.

Brief Patent Description - Full Patent Description - Patent Application Claims
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The invention is in the technical field of crop protection products which can be employed against harmful plants, for example in crop plants, and which comprise, as active compounds, a combination of at least two herbicides.

The documents WO 92/13845 and WO 95/10507 disclose sulfonylureas and their salts and also their use as herbicides and/or plant growth regulators.

The efficacy of these herbicides against harmful plants in the crop plants is at a high level, but depends in general on the application rate, the formulation in question, the harmful plants or spectrum of harmful plants to be controlled in each case, the climatic conditions, the soil conditions and the like. Another criterion is the duration of action, or the breakdown rate of the herbicide. If appropriate, changes in the sensitivity of harmful plants, which may occur upon prolonged use of the herbicides or within geographic limitations must also be taken into consideration. The compensation of losses in action in the case of individual harmful plants by increasing the application rates of the herbicides is only possible to a certain degree, for example because such a procedure frequently reduces the selectivity of the herbicides or because the action is not improved, even when applying higher rates. In some cases, the selectivity in crops can be improved by adding safeners. In general, however, there remains a need for methods to achieve the herbicidal action with a lower application rate of active compounds. Not only does a lower application rate reduce the amount of an active compound required for application, but, as a rule, it also reduces the amount of formulation auxiliaries required. It both reduces the economic input and improves the ecological compatibility of the herbicide treatment.

One possibility of improving the application profile of a herbicide can consist in combining the active compound with one or more other active compounds. However, the combined use of a plurality of active compounds frequently causes phenomena of physical and biological incompatibility, for example a lack of stability in a coformulation, decomposition of an active compound, or antagonism of the active compounds. What is desired are, in contrast, combinations of active compounds having an advantageous activity profile, high stability and, if possible, a synergistically improved action, which allows the application rate to be reduced in comparison with the individual application of the active compounds to be combined.

Surprisingly, it has now been found that certain active compounds from the group of the sulfonylureas or their salts in combination with certain structurally different herbicides act together in a particularly advantageous manner, for example when they are employed in crop plants which are suitable for the selective use of the herbicides, if appropriate with addition of safeners.

The invention therefore provides herbicide combinations comprising an effective amount of components (A) and (B), where (A) denotes one or more herbicides selected from the group of the compounds of the formula (I) and their salts

in which

  • R1 is (C1-C8)-alkyl, (C3-C4)-alkenyl, (C3-C4)-alkynyl or (C1-C4)-alkyl which is mono- to tetrasubstituted by radicals selected from the group consisting of halogen and/or (C1-C2)-alkoxy, preferably (C1-C4)-alkyl,
  • R2 is I or CH2NHSO2CH3,
  • R3 is methyl or methoxy and
  • z is N or CH;
    and
  • (B) denotes one or more herbicides which act selectively in some monocotyledonous crops against monocotyledonous and/or dicotyledonous harmful plants, which herbicides are selected from the group of compounds consisting of (refer to by the common name, and with a literature reference, for example from “The Pesticide Manual”, 12th Ed., British Crop Protection Council 2000, abbreviated as “PM”)
    • (B1) flucarbazone, in particular also comprising its salts, such as the sodium salt (PM, pp. 427-428), for example 4,5-dihydro-3-methoxy-4-methyl-5-oxo-N-(2-trifluoromethoxyphenylsulfonyl)-1H-1,2,4-triazole-1-carboxamide sodium salt (application rate generally: 1-500 g of AS/ha, preferably 5-200 g of AS/ha; ratio of application rates A:B generally 1:200-5:1, preferably 1:100-2:1);
    • (B2) BAY MKH 6561 (procarbazone), in particular also comprising its esters and salts, such as the sodium salt (Z. PflKrankh. PflSchutz, special edition XVII, 545-553 (2000)), for example methyl 2-({[(4-methyl-5-oxo-3-propoxy-4,5-dihydro-1H-1,2,4-triazol-1-yl)carbonyl]amino}sulfonyl)benzoate sodium salt (application rate generally: 1-500 g of AS/ha, preferably 5-200 g of AS/ha; ratio of application rates A:B generally =1:200-5:1, preferably 1:100-2:1);


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