The present invention provides a spreading agent for agrochemicals having superior adhesion particularly for plant surface. The present invention also provides an agrochemical spray solution having a reduced risk of leaving the spreading agent for agrochemicals on a plant surface. The present invention relates to a spreading agent for agrochemicals comprising a carboxy-modified vinyl alcohol polymer (A) having a carboxy-containing monomer unit content of 0.1 mol % to 10 mol %, a viscosity-average degree of polymerization of 200 to 5,000, and a degree of saponification of 65 mol % to 99.9 mol %.

Compositions and methods for controlling nematodes are described herein, e.g., nematodes that infest plants or animals. The compounds include oxazoles, oxadiazoles and thiadiazoles.

Compositions and methods for controlling nematodes are described herein, e.g., nematodes that infest plants or animals. The compounds include oxazoles, oxadiazoles and thiadiazoles.

Disclosed are compounds of Formula 1, including all geometric and stereoisomers, N-oxides, and salts thereof, ##STR00001##
wherein Q is ##STR00002##
and A, R.sup.1, m, X.sup.1, X.sup.2, Y.sup.1, Y.sup.2, Y.sup.3 and R.sup.5a are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound or a composition of the invention.

Solvent formulations under EC form comprising (% by weight): 10-40% of one or more compounds having an insecticidal activity selected from the organophosphate class; 1-20% of an additive (A) methyl or ethyl esters of carboxylic acids having a C.sub.10-C.sub.20 chain, saturated or unsaturated, or mixtures thereof, the fatty acids deriving from vegetal oils; 0.5-10% of an additive B) of a cellulose derivative soluble in the organic solvent of EC formulation; 3-15% of one or more surfactants selected from non ionic and anionic surfactants, or thereof mixtures; the complement to 100% being of one or more organic solvents having the following characteristics: capable to solubilize the active principle, expressed as % by weight, at room temperature (20-25 C.) for at least 5%; preferably 10%, more preferably at least 20%, immiscible with water.

Solvent formulations under EC form comprising (% by weight): 10-40% of one or more compounds having an insecticidal activity selected from the organophosphate class; 1-20% of an additive (A) methyl or ethyl esters of carboxylic acids having a C.sub.10-C.sub.20 chain, saturated or unsaturated, or mixtures thereof, the fatty acids deriving from vegetal oils; 0.5-10% of an additive B) of a cellulose derivative soluble in the organic solvent of EC formulation; 3-15% of one or more surfactants selected from non ionic and anionic surfactants, or thereof mixtures; the complement to 100% being of one or more organic solvents having the following characteristics: capable to solubilize the active principle, expressed as % by weight, at room temperature (20-25 C.) for at least 5%; preferably 10%, more preferably at least 20%, immiscible with water.

Described herein are mixtures including as active components at least one specific nitrification inhibitor (compound I) and at least one urease inhibitor (compound II). Also described herein are a method for improving the nitrification-inhibiting effect, or for increasing the health of a plant using mixtures of at least one compound I and at least one compound II and a method of using the mixtures comprising compounds I and compounds II for increasing the health of a plant. Also described herein are agrochemical compositions including these mixtures. Also described herein is plant propagation material including these mixtures or these agrochemical compositions.

Described herein are mixtures including as active components at least one specific nitrification inhibitor (compound I) and at least one urease inhibitor (compound II). Also described herein are a method for improving the nitrification-inhibiting effect, or for increasing the health of a plant using mixtures of at least one compound I and at least one compound II and a method of using the mixtures comprising compounds I and compounds II for increasing the health of a plant. Also described herein are agrochemical compositions including these mixtures. Also described herein is plant propagation material including these mixtures or these agrochemical compositions.

Described herein are mixtures including as active components at least one specific nitrification inhibitor (compound I) and at least one urease inhibitor (compound II). Also described herein are a method for improving the nitrification-inhibiting effect, or for increasing the health of a plant using mixtures of at least one compound I and at least one compound II and a method of using the mixtures comprising compounds I and compounds II for increasing the health of a plant. Also described herein are agrochemical compositions including these mixtures. Also described herein is plant propagation material including these mixtures or these agrochemical compositions.

Preparation of O,O-dimethyl phosphoramidothioate and O,O-dimethyl phosphoroamidothioate. A process of making O,O-dimethyl phosphoroamidothioate is described including reacting sulfur with PCl.sub.3 to form PSCl.sub.3, reacting the PSCl.sub.3 formed with methanol to form O-methyl phosphorodichloridothioate, and reacting the O-methyl phosphorodichloridothioate formed with methyl lye to form O,O-dimethyl phosphorochloridothioate in solution in CH.sub.2Cl.sub.2, and reacting the O,O-dimethyl phosphorochloridothioate formed with sodium hydroxide and ammonium hydroxide to form O,O-dimethyl phosphoroamidothioate in solution in CH.sub.2Cl.sub.2. Reacting the O,O-dimethyl phosphoroamidothioate formed with catalytic dimethyl sulfate to form methamidophos and reacting the methamidophos formed with acetic anhydride to form N-(methoxy-methylsulfanylphosphoryl) acetamide is also described. Throughout the process, the O,O-dimethyl phosphorochloridothioate and the O,O-dimethyl phosphoroamidothioate formed are maintained in solution in CH.sub.2Cl.sub.2 at all times.