The invention relates to herbicidal active compound combinations comprising, carbamoyltriazolinones, and herbicidally active compounds, which combinations are suitable for controlling weeds.

The invention relates to herbicidal active compound combinations comprising, carbamoyltriazolinones, and herbicidally active compounds, which combinations are suitable for controlling weeds.

The present invention is directed to new uses of the herbicidal active compound 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (compound I) as foliar herbicide. Furthermore, the present invention is directed to combinations comprising active compound 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (compound I) and to a method for controlling undesired weeds by applying the herbicidal active compound 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (compound I) or combinations comprising compound I to weeds or to the area in which the weeds grow after emergence of the crop.

The present invention is directed to new uses of the herbicidal active compound 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (compound I) as foliar herbicide. Furthermore, the present invention is directed to combinations comprising active compound 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (compound I) and to a method for controlling undesired weeds by applying the herbicidal active compound 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (compound I) or combinations comprising compound I to weeds or to the area in which the weeds grow after emergence of the crop.

The present application discloses herbicidal compositions containing a first herbicide beflubutamid, or an optically enriched form thereof, and a second herbicide selected from WSSA Group 15 herbicides, WSSA Group 13 herbicides, WSSA Group 27 herbicides, WSSA Group 9 herbicides, WSSA Group 10 herbicides, WSSA Group 22 herbicides, WSSA Group 7 herbicides, WSSA Group 3 herbicides, WSSA Group 14 triazolinone herbicides, WSSA Group 1 cyclohexanedione herbicides, WSSA Group 2 imidazolinone herbicides, WSSA Group 14 N-phenylphthalimide herbicides, WSSA Group 14 diphenylether herbicides, WSSA Group 14 pyrimidinedione herbicides, WSSA Group 5 1,2,4-triazine herbicides and herbicides selected from metamifop, atrazine, fenoxaprop-P-ethyl, 2,4-D (2,4-dichlorophenoxyacetic acid), florasulam, halosulfuron-methyl and prosulfocarb. The application also discloses a method of controlling undesired vegetation in a crop by applying to the locus of such vegetation a herbicidally effective amount of a herbicidal composition.

The present application discloses herbicidal compositions containing a first herbicide beflubutamid, or an optically enriched form thereof, and a second herbicide selected from WSSA Group 15 herbicides, WSSA Group 13 herbicides, WSSA Group 27 herbicides, WSSA Group 9 herbicides, WSSA Group 10 herbicides, WSSA Group 22 herbicides, WSSA Group 7 herbicides, WSSA Group 3 herbicides, WSSA Group 14 triazolinone herbicides, WSSA Group 1 cyclohexanedione herbicides, WSSA Group 2 imidazolinone herbicides, WSSA Group 14 N-phenylphthalimide herbicides, WSSA Group 14 diphenylether herbicides, WSSA Group 14 pyrimidinedione herbicides, WSSA Group 5 1,2,4-triazine herbicides and herbicides selected from metamifop, atrazine, fenoxaprop-P-ethyl, 2,4-D (2,4-dichlorophenoxyacetic acid), florasulam, halosulfuron-methyl and prosulfocarb. The application also discloses a method of controlling undesired vegetation in a crop by applying to the locus of such vegetation a herbicidally effective amount of a herbicidal composition.

Techniques regarding chemical compounds with antimicrobial functionality are provided. For example, one or more embodiments describe herein can comprise a monomer that can comprise a molecular backbone. The molecular backbone can comprise a bis(urea)guanidinium structure covalently bonded to a functional group, which can comprise a radical. Also, the monomer can have supramolecular assembly functionality.

Techniques regarding chemical compounds with antimicrobial functionality are provided. For example, one or more embodiments describe herein can comprise a monomer that can comprise a molecular backbone. The molecular backbone can comprise a bis(urea)guanidinium structure covalently bonded to a functional group, which can comprise a radical. Also, the monomer can have supramolecular assembly functionality.

The present invention is directed to new uses of the herbicidal active compound 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (compound I) as foliar herbicide. Furthermore, the present invention is directed to combinations comprising active compound 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (compound I) and to a method for controlling undesired weeds by applying the herbicidal active compound 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (compound I) or combinations comprising compound I to weeds or to the area in which the weeds grow after emergence of the crop.

The present invention is directed to new uses of the herbicidal active compound 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (compound I) as foliar herbicide. Furthermore, the present invention is directed to combinations comprising active compound 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (compound I) and to a method for controlling undesired weeds by applying the herbicidal active compound 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (compound I) or combinations comprising compound I to weeds or to the area in which the weeds grow after emergence of the crop.