Abstract: The invention relates to a solid crop protection formulation comprising

Abstract: The present invention relates to crystalline hydrates substituted nicotinanilinde derivatives, to their preparation, and to their use for controlling phytopathogenic fungi or undesired attack by insects or mites and/or for regulating the growth of plants.

Abstract: The invention relates to a solid crop protection formulation comprising

Abstract: The present invention relates to an agrotechnical formulation which comprises, in each case based on the total weight of the formulation: a) 20 to 99.9% by weight of at least one cyclohexanepolycarboxylic ester of the formula I  in which R1 is C1-C10-alkyl or C3-C8-cycloalkyl; m is 0, 1, 2 or 3; and n is 2, 3 or 4; and R is H or C1-C30-alkyl, where at least one radical R is C1-C30-alkyl; b) 0 to 70% by weight of water; c) 0.1 to 60% by weight of at least one adjuvant and/or additive; and d) 0 to 70% by weight of at least one active ingredient for plant treatment.

Abstract: A process for the preparation of a solvent-free suspension of a low-melting point water-insoluble solid agrochemical active ingredient, which comprises suspending 1-40% by weight of a silica-based carrier in 40 to 97% by weight of water in the presence of 1-40% by weight of anionic dispersant, heating the suspension thus obtained to a temperature above that of the active ingredient, and adding, with stirring, 1-25% by weight of a molten active ingredient with a melting point of <80° C. or a mixture of at least two active ingredients each having a melting point of <80° C. The present invention furthermore relates to the preparation of suspension concentrates, water-dispersible powders and water-dispersible granules based on the suspensions prepared via the abovementioned process.

Abstract: Solid mixtures comprising a) an active ingredient from the group of the sulfonylureas and b) a sulfate- or sulfonate-containing surfactant.

Abstract: The present invention relates to an agrotechnical formulation which comprises, in each case based on the total weight of the formulation:

Abstract: Solid formulation of a crop protection product can be obtained by melt extrusion and shaping of a mixture consisting of: 0.1-80% by wt. of an active ingredient which can be used in crop protection, or of a combination of such active ingredients, 10-80% by wt. of at least one mineral filler, 0-20% by wt. of inorganic or organic additives, and to 100% by wt.

Abstract: A herbicidal mixture, comprising a) a herbicidally effective amount of a benzoyl compound of formula I  where: R1, R2 are halogen, C1-C6-alkyl, C1-C6-alkylthio, C1-C6-alkyl-sulfinyl or C1-C6-alkylsulfonyl; R3 is hydrogen, halogen, C1-C6-alkyl; X is 4,5-dihydroisoxazolyl which is unsubstituted or mono- or polysubstituted by halogen, C1-C6-alkyl, C1-C4-alkoxy, C1-C4-haloalkyl, C1-C4-haloalkoxy, C1-C4-alkylthio; R4 is a pyrazole of the formula II  which is attached in the 4-position and where R5 is hydrogen, R6 is methyl, or an environmentally compatible salt thereof; b) an adjuvant comprising i) a C1-C5-alkyl C5-C22-alkanoate, ii) a C10-C20-carboxylic acid, iii) a partial phosphoric ester or a partial sulfuric ester of a monohydroxy-functional polyalkyl ether and iv) optionally an alkyl polyoxyalkylene polyether, wherein the compound of formula I and the adjuvat are present in synergistically effective amounts.

Abstract: Solid mixtures comprising a) an active compound from the group consisting of the sulfonylureas, and b) an alkylpolyglucoside.

Abstract: A herbicidal mixture comprising a) a herbicidally active amount of a 3-heterocyclyl-substituted benzoyl derivative of the formula I  in which the variables have the following meanings: R1,R2 are hydrogen, halogen, C1-C6-alkyl, C1-C6-alkylthio, C1-C6-alkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy; R3 is hydrogen, halogen, C1-C6-alkyl; X is a heterocycle from amongst the group consisting of isoxazolyl, 4,5-dihydroisoxazolyl and thiazolyl, it being possible for the heterocycle to be optionally monosubstituted or polysubstituted by halogen, C1-C6-alkyl, C1-C4-alkoxy, C1-C4-haloalkyl, C1-C4-haloalkoxy, C1-C4-alkylthio; R5 is hydrogen or C1-C6-alkyl, R6 is C1-C6-alkyl, or their environmentally compatible salts; b) a nitrogenous fertilizer in a synergistically effective amount and c) an adjuvant in a synergistically effective amount.

Abstract: Solid mixtures comprising

Abstract: A substantially water-free formulation of crop protection agents, comprising essentially a) a cyclohexenone oxime ether of the formula I  where R1=ethyl, propyl; R2=hydrogen or an equivalent of an agriculturally useful cation; R3=2-(thioethyl)propyl, tetrahydrothiopyran-3-yl, tetrahydrothiopyran-4-yl, tetrahydropyran-3-yl, tetrahydropyran-4-yl, 1-(methylthio)cyclopropyl, 5-(isopropyl)isoxazol-3-yl, 2,5-dimethylpyrazol-3-yl, 2,4,6-trimethylphenyl or 2,4,6-trimethyl-3-butyrylphenyl; R4, R5=H, CH3, CO—OCH3; Alk=CH2CH2, CH2CH(CH3), CH2CH═CH, CH2CH═C(Cl), CH2CH2CH═CH; R6=H, phenyl, halophenyl, dihalophenyl, phenoxy, halophenoxy, dihalophenoxy; b) N-phosphonamethylglycine, or an ester or salt thereof, DL-homoalanin-4-yl(methyl)phosphinic acid or its ammonium salt; c) from 20 to 80% by weight of an aprotic or weakly protic solvent in which the components a) and b) are suspended; d) if desired emulsifiers, surfactants, sur

Abstract: A process for improvement of the soil by reducing microbially formed ethylene in the soil by bringing compounds which bind ethylene or of which it is known that they inhibit ethylene biosynthesis between S-adenosyl-L-methionine and 1-aminocyclopropane-carboxylic acid or 1-aminocyclopropane-1-carboxylic acid and ethylene respectively, into the soil zone relevant for the root growth of higher plants and allowing them to act there on the soil microorganisms.

Abstract: Storage-stable aqueous formulations comprising a) 0.1-60% by weight of a tetrahydrophthalimide of the formula I  where R1=H, F, Cl; R2=CH═C(Cl)—CO—B or CH═C(Br)—CO—B (B=C1-C6-alkyl, unsubstituted or substituted OH or SH); a group OR5, SR5, COOR5, OCH2COOR5, CH2—CO—OR6 or (C1-C6-alkyl)sulfonylamino; R5=H, C1-C6-alkyl, C3-C7-cycloalkyl, C2-C8-alkenyl, C2-C6-alkynyl, (C1-C6-alkoxy)carbonyl-C1-C6-alkyl or C1-C6-alkyloximino-C1-C6-alkyl R3=Cl, CN; R6=is H, C1-C6-alkyl, C2-C8-alkenyl, C2-C6-alkynyl, C3-C7-cycloalkyl, C1-C6-alkoxy-C1-C6-alkyl or C1-C6-alkyloximino-C1-C6-alkyl; b) 0.1-30% by weight of an anionic surfactant; c) 0.1-30% by weight of a non-ionic surfactant; d) 0.01-5% by weight of a thixotroping additive; e) 0-50% by weight of other herbicidal active ingredients; f) 0-20% by weight of other formulation auxiliaries, and g) 1-90% of water.

Abstract: A solid ixture comprising a) an active ingredient from the group of the sulfonylureas and b) an alkyl ether of a copolymer of C2-C4-alkylene oxides.

Abstract: A liquid formulation of cinidon-ethyl, i.e., ethyl (Z)-2-chloro-3-[2-chloro-5 -(4,5,6,7-tetrahydro-1,3-dioxoisoindoledion-2-yl)phenyl] acrylate comprising, essentially, in addition to the above crop protection agent, a) an ionic emulsifier, b) a non-ionic emulsifier, c) a non-nucleophilic and non-basic aromatic solvent and, d) if desired, a further herbicidal crop protection agent, and a method of controlling undesirable vegetation using this formulation.

Abstract: A solid mixture comprising A) 3-isopropyl-2,1,3-benzothiadiazine-4-one 2,2-dioxide or a salt thereof and B) at least one nonionic surfactant, a process for its preparation, and its use for controlling undesirable vegetation.

Abstract: Herbicidally active cyclohexenone oxime ether metal salts of formula I ##STR1## where R.sup.a, R.sup.b, R.sup.c, R.sup.d, R.sup.e, Alk and R.sup.f are as defined in the specification disclosure, having an improved shelf life and thermal stability and reduced water vapor uptake.

Abstract: Crop protection active compound formulations, comprising a cyclohexenone oxime ether of the general formula I ##STR1## where the radicals R.sup.1 -R.sup.6 have the following meanings: R.sup.1 is ethyl or propyl;R.sup.2 is hydrogen or an equivalent of an agriculturally utilizable cation;R.sup.3 is 2-thioethylpropyl, tetrahydrothiopyran-3-yl, tetrahydrothiopyran-4-yl, tetrahydropyran-3-yl, tetrahydropyran-4-yl, 1-methylthiocyclopropyl, 5-isopropylisoxazol-3-yl, 2,5-dimethylpyrazol-3-yl, 2,4,6-trimethylphenyl or 2,4,6-trimethyl-3-butyrylphenyl;R.sup.4 and R.sup.5 independently of one another are hydrogen, methyl or methoxycarbonyl;Alk is CH.sub.2 CH.sub.2, CH.sub.2 CH(CH.sub.3), CH.sub.2 CH.dbd.CH, CH.sub.2 CH.dbd.C(Cl) or CH.sub.2 CH.sub.2 CH.dbd.CH;R.sup.6 is hydrogen, phenyl, halophenyl, dihalophenyl, phenoxy, halophenoxy or dihalophenoxy;and a water-soluble basic salt of an acid having a pK.sub.