Abstract: A fungicidal composition containing a fungicidally effective amount of the compound of Formula I: 5-fluoro-4-imino-3-methyl-1-tosyl-3,4-dihydropyrimidin-2(1H)-one, and at least one fungicide to provide synergistic control of selected fungi wherein the at least one fungicide is a fungicidal sterol biosynthesis-inhibitor.

Abstract: A fungicidal composition containing a fungicidally effective amount of the compound of Formula I: 5-fluoro-4-imino-3-methyl-1-tosyl-3,4-dihydropyrimidin-2(1H)-one, and at least one fungicide to provide synergistic control of selected fungi wherein the at least one fungicide is a multi-site inhibitor or a strobilurin inhibitor.

Abstract: The invention relates to a method for the preparation of 2-aminobiphenyls, key intermediates in the preparation of compounds of interest in the agrochemical industry. The process comprises reacting an ortho-substituted aniline and a phenylboro derivative in the presence of a base and a palladium catalyst, said palladium catalyst comprising a palladium source and a biphenyl phosphine ligand of formula (III) or a salt thereof.

Abstract: The present invention relates to a stable concentrated agrochemical suspension comprising SDHI fungicide and/or strobilurin fungicide and stabilizing component comprising a) at least one naphthalenesulfonate condensate; b) at least one fatty alcohol alkoxylate; c) at least one block copolymer; d) optionally at least one organomodified polysiloxane; 3) water; and use of said concentrated suspension as a fungicide in agrochemical field.

Abstract: A fungicidal composition containing a fungicidally effective amount of the compound of Formula I: 5-fluoro-4-imino-3-methyl-1-tosyl-3,4-dihydropyrimidin-2(1H)-one, and at least one fungicide to provide synergistic control of selected fungi wherein the at least one fungicide is a fungicidal sterol biosynthesis-inhibitor.

Abstract: The present invention provides fungicidal combination comprising: (i) an amount of a compound of Formula I and (ii) an amount of at least one fungicide (A) selected from the group consisting of pyrimidines, antibiotics, anilinopyrimidines (AP), aromatic hydrocarbons, aryl-phenylketones, azanaphthalenes, benzamides, benzenesulfonamides, benzo-thiadiazoles (BTH), carboxylic acid amides (CAA), carbamates, cyanoacetamideoxime, dicarboximides, dithiolanes, growth regulators, guanidines, heteroaromatics, inorganics, methyl benzimidazole carbamates (MBC), melanin biosynthesis inhibitors (MBI), membrane disruptors, organo tin compounds, oxysterol binding protein homologue inhibition (OSBPI), phenylamides (PA), phenylacetamides, phenylureas, phosphonates, polyoxins, phenylpyrroles, uncouplers of oxidative phosphorylation, dithianon, sulphur, bordeaux-mixture, thiram, zineb, ziram, famoxadone, fenamidone, pyribencarb, ametoctradin, diniconazole, penconazole, triadimefon, triadimenol, triflumizole, bromuconazole, im

Abstract: The present invention relates to novel di-imine, oxadiazepine and oxadiazine intermediates as key intermediates for preparation of oxadiazine insecticides, the processes of their preparation, purification and use in the preparation of final oxadiazine pesticides, in particular of indoxacarb. Telescopic process of preparation of arthropocidal oxadiazines, in particular indoxacarb is disclosed.

Abstract: The present disclosure relates to solid state forms of Indoxacarb or its solvate, processes for preparation thereof and agrochemical compositions thereof.

Abstract: The present invention provides improved combinations, mixtures and compositions comprising a phthalimide fungicide and at least one primary fungicide selected from pyrimidinone fungicide, QiI (quinone inside inhibitors), QoI (quinone outside inhibitors), SDHI (succinate dehydrogenase inhibitors), DMI fungicide (demethylation inhibitor fungicide), OSBPI (oxysterol binding protein inhibitor), amine fungicide, tetrazolyloxime fungicide, phenylpyridinamine fungicide, or inorganic fungicide and any combination thereof, as well as methods of use and processes of preparation thereof.

Abstract: The present invention relates to an improved process for the industrial-scale production process of Tau-fluvalinate in a purified form comprising optimization of the reaction conditions by timely acid neutralization, resulting in preventing corrosions of the expensive plant equipment.

Abstract: The present invention relates to insecticidal combinations comprising a) an anthranilamide compound of formula (I) and b) tau-fluvalinate.

Abstract: The present invention provides combinations and compositions comprising (1) copper-based fungicide, (2) azole fungicide and (3) compatibility agent, preferably wherein the compatibility agent is a compound (I) selected from the group consisting of thiourea-based compound, sodium thiosulfate, alkyl amine, thioamide-based compound and any combination thereof. The present invention also provides process of preparing and methods of using said combinations and compositions.

Abstract: The present invention provides a method for neutralizing the odor (purifying), of a technical phthalimide-based fungicide comprising (1) mixing (i) slurry of phthalimide-based fungicide in water with (ii) ammonium hydroxide solution, preferably followed by, (2) filtration of the phthalimide-based fungicide and (3) drying.

Abstract: The present invention relates pesticidal complexes, pesticidal delivery systems and compositions, as well as processes of preparation and uses thereof. The present invention also relates to the use of cyclodextrins for increasing biological activity and improving uptake, penetration, retention and/or bioavailability of agrochemicals such as pesticides.

Abstract: An aqueous pesticidal suspension composition comprising a macrolide insecticidal compound or salt thereof; at least one polycationic rheology modifier; optionally additives and optionally additional active ingredient.

Abstract: The present disclosure provides a process for preparing 5-chloro-2,3-dihydro-1H-inden-1-one and the 5-chloro-2,3-dihydro-1H-inden-1-one prepared by the process. The present disclosure also provides a process for preparing Indoxacarb and the Indoxacarb prepared by the process.

Abstract: The present invention provides a method of preventing leakage of an aromatic compound from an article containing a formulation comprising the aromatic compound and a polar liquid, wherein the method comprises plasma-coating the article.

Abstract: The present invention relates to stable combined dispersions of at least one dithiocarbamate fungicide and at least one acid-based pesticide, and/or derivative thereof in a liquid carrier, wherein said dispersion is stabilized by inclusion of at least one organic phosphoric acid ester-based compatibility agent and wherein said dispersion is characterized by an improvement in the stability, compatibility, and suspensibility of the dispersion defined by a reduction in the rate and/or extent of phase separation and/or sedimentation. The invention further relates to methods for preparing and using said combined dispersions and methods for identifying useful organic phosphoric acid ester-based compatibility agents.

Abstract: A fungicidal composition containing a fungicidally effective amount of the compound of Formula I: 5-fluoro-4-imino-3-methyl-1-tosyl-3,4-dihydropyrimidin-2(1H)-one, and at least one fungicide to provide synergistic control of selected fungi, wherein the at least one fungicide is a succinate dehydrogenase-inhibitor.

Abstract: The present invention provides a method for controlling the degradation of emamectin and cartap, the method comprising formulating a composition which comprises an amount of water less than 0.5% by weight based on the total weight of the stable composition and at least one pH adjuster for maintaining the pH at 25° C. after dilution in water at less than 5.5. The present invention further provides a stable solid insecticidal composition comprising: (1) an effective amount of emamectin; (2) an effective amount of cartap; and (3) at least one pH adjuster; wherein the composition is substantially free of water and the pH at 25° C. after dilution with water is less than 5.5.