A01N37/08

USE OF N-SUBSTITUTED PYRROLIDONES TO PROMOTE THE PENETRATION OF AGROCHEMICAL ACTIVE AGENTS

Disclosed herein is a method for promoting the penetration of at least one active agrochemical ingredient into a plant. The method includes the step of contacting the plant with a crop protection composition containing N-(n-butyl)-2-pyrrolidone and the at least one active agrochemical ingredient.

Foam formulations and apparatus for delivery

Foamable formulations of agriculturally active ingredients are provided, as well as methods for using them. The formulations allow improved delivery active ingredients by the ability to deliver high amounts of active ingredient with a low volume of formulation used.

Foam formulations and apparatus for delivery

Foamable formulations of agriculturally active ingredients are provided, as well as methods for using them. The formulations allow improved delivery active ingredients by the ability to deliver high amounts of active ingredient with a low volume of formulation used.

Fungicidal compositions comprising a carboxamide

A method of controlling phytopathogenic diseases on useful plants or on propagation material thereof, which comprises applying to the useful plants, the locus thereof or propagation material thereof a combination of components (A) and (B) in a synergistically effective amount, wherein component (A) is a compound of formula I compound of formula I ##STR00001## wherein R is hydrogen or methoxy; Q is ##STR00002## R.sub.1 is hydrogen, halogen or C.sub.1-C.sub.6alkyl; R.sub.2 is hydrogen, halogen, C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6alkenyl, C.sub.3-C.sub.6alkinyl, C.sub.3-C.sub.6cycloalkyl-C.sub.3-C.sub.6alkinyl, halophenoxy, halophenyl-C.sub.3-C.sub.6alkinyl, C(C.sub.1-C.sub.4alkyl)=NOC.sub.1-C.sub.4alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6haloalkoxy, C.sub.2-C.sub.6haloalkenyl, or C.sub.2-C.sub.6haloalkenyloxy; R.sub.3 is hydrogen, halogen, C.sub.1-C.sub.6alkyl; R.sub.4, R.sub.5 and R.sub.6, independently from each other, are hydrogen, halogen or --R.sub.7; with the proviso that at least one of R.sub.4, R.sub.5 and R.sub.6 is different from hydrogen; R.sub.7 is hydrogen, C.sub.1-C.sub.6alkyl, C.sub.1-C.sub.6haloalkyl or C.sub.1-C.sub.4alkoxyalkyl; and R.sub.8 is hydrogen or methoxy; and agrochemically acceptable salts/isomers/structural isomers/stereoisomers/diastereoisomers/enantiomers/tautomers and N-oxides of those compounds; and component (B) is a compound selected from compounds known for their fungicidal and/or insecticidal activity, is particularly effective in controlling or preventing fungal diseases of useful plants.

Fungicidal compositions comprising a carboxamide

A method of controlling phytopathogenic diseases on useful plants or on propagation material thereof, which comprises applying to the useful plants, the locus thereof or propagation material thereof a combination of components (A) and (B) in a synergistically effective amount, wherein component (A) is a compound of formula I compound of formula I ##STR00001## wherein R is hydrogen or methoxy; Q is ##STR00002## R.sub.1 is hydrogen, halogen or C.sub.1-C.sub.6alkyl; R.sub.2 is hydrogen, halogen, C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6alkenyl, C.sub.3-C.sub.6alkinyl, C.sub.3-C.sub.6cycloalkyl-C.sub.3-C.sub.6alkinyl, halophenoxy, halophenyl-C.sub.3-C.sub.6alkinyl, C(C.sub.1-C.sub.4alkyl)=NOC.sub.1-C.sub.4alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6haloalkoxy, C.sub.2-C.sub.6haloalkenyl, or C.sub.2-C.sub.6haloalkenyloxy; R.sub.3 is hydrogen, halogen, C.sub.1-C.sub.6alkyl; R.sub.4, R.sub.5 and R.sub.6, independently from each other, are hydrogen, halogen or --R.sub.7; with the proviso that at least one of R.sub.4, R.sub.5 and R.sub.6 is different from hydrogen; R.sub.7 is hydrogen, C.sub.1-C.sub.6alkyl, C.sub.1-C.sub.6haloalkyl or C.sub.1-C.sub.4alkoxyalkyl; and R.sub.8 is hydrogen or methoxy; and agrochemically acceptable salts/isomers/structural isomers/stereoisomers/diastereoisomers/enantiomers/tautomers and N-oxides of those compounds; and component (B) is a compound selected from compounds known for their fungicidal and/or insecticidal activity, is particularly effective in controlling or preventing fungal diseases of useful plants.

PESTICIDE SYNERGIST SX-PYR
20250324969 · 2025-10-23 ·

The present invention relates to a composition and to the production and use of said composition.

Pesticide synergist composition containing, among others, (1) a cysteine proteolytic enzyme (or a mixture of cysteine proteolytic enzymes), (2) a polyphenolic compound (or a mixture of polyphenolic compounds chosen from among hydrolysable tannins), (3) a compound chosen from among the triglycerides (or a mixture thereof), (4) a phase change inhibitor chosen from among (ethanol, isopropyl alcohol, benzylic alcohol and the mixtures thereof), (5) an enzyme stabilizer chosen from among the organic peroxides, (6) a non-ionic surfactant, (7) an essential oil chosen from among the essential oils of Melaleuca alternifolia and quinquenervia, (9) a simple reagent such as acetic acid and citric acid to modify/stabilize the pH the present invention may be in the form of a concentrate or an emulsion containing pyrethrins (pyrethrum flower extract), pyrethroids (i) and (ii), and a mixture thereof. said composition is intended for use in managing the resistance associated with the mechanisms of insects for detoxifying insecticides and to improve the efficiency of certain insecticides, in particular certain insecticides such as pyrethrins and pyrethroids (i) and (ii).

PESTICIDE SYNERGIST SX-PYR
20250324969 · 2025-10-23 ·

The present invention relates to a composition and to the production and use of said composition.

Pesticide synergist composition containing, among others, (1) a cysteine proteolytic enzyme (or a mixture of cysteine proteolytic enzymes), (2) a polyphenolic compound (or a mixture of polyphenolic compounds chosen from among hydrolysable tannins), (3) a compound chosen from among the triglycerides (or a mixture thereof), (4) a phase change inhibitor chosen from among (ethanol, isopropyl alcohol, benzylic alcohol and the mixtures thereof), (5) an enzyme stabilizer chosen from among the organic peroxides, (6) a non-ionic surfactant, (7) an essential oil chosen from among the essential oils of Melaleuca alternifolia and quinquenervia, (9) a simple reagent such as acetic acid and citric acid to modify/stabilize the pH the present invention may be in the form of a concentrate or an emulsion containing pyrethrins (pyrethrum flower extract), pyrethroids (i) and (ii), and a mixture thereof. said composition is intended for use in managing the resistance associated with the mechanisms of insects for detoxifying insecticides and to improve the efficiency of certain insecticides, in particular certain insecticides such as pyrethrins and pyrethroids (i) and (ii).

FUNGICIDAL COMPOSITIONS COMPRISING A CARBOXAMIDE
20260000083 · 2026-01-01 · ·

A method of controlling phytopathogenic diseases on useful plants or on propagation material thereof, which comprises applying to the useful plants, the locus thereof or propagation material thereof a combination of components (A) and (B) in a synergistically effective amount, wherein component (A) is a compound of formula I compound of formula I

##STR00001## wherein R is hydrogen or methoxy; Q is

##STR00002## R.sub.1 is hydrogen, halogen or C.sub.1-C.sub.6alkyl; R.sub.2 is hydrogen, halogen, C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6alkenyl, C.sub.3-C.sub.6alkinyl, C.sub.3-C.sub.6cycloalkyl-C.sub.3-C.sub.6alkinyl, halophenoxy, halophenyl-C.sub.3-C.sub.6alkinyl, C(C.sub.1-C.sub.4alkyl)=NO-C.sub.1-C.sub.4alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6haloalkoxy, C.sub.2-C.sub.6haloalkenyl, or C.sub.2-C.sub.6haloalkenyloxy; R.sub.3 is hydrogen, halogen, C.sub.1-C.sub.6alkyl; R.sub.4, R.sub.5 and R.sub.6, independently from each other, are hydrogen, halogen or --R.sub.7; with the proviso that at least one of R.sub.4, R.sub.5 and R.sub.6 is different from hydrogen; R.sub.7 is hydrogen, C.sub.1-C.sub.6alkyl, C.sub.1-C.sub.6haloalkyl or C.sub.1-C.sub.4alkoxyalkyl; and R.sub.8 is hydrogen or methoxy; and agrochemically acceptable salts/isomers/structural isomers/stereoisomers/diastereoisomers/enantiomers/tautomers and N-oxides of those compounds; and component (B) is a compound selected from compounds known for their fungicidal and/or insecticidal activity, is particularly effective in controlling or preventing fungal diseases of useful plants.

FUNGICIDAL COMPOSITIONS COMPRISING A CARBOXAMIDE
20260000083 · 2026-01-01 · ·

A method of controlling phytopathogenic diseases on useful plants or on propagation material thereof, which comprises applying to the useful plants, the locus thereof or propagation material thereof a combination of components (A) and (B) in a synergistically effective amount, wherein component (A) is a compound of formula I compound of formula I

##STR00001## wherein R is hydrogen or methoxy; Q is

##STR00002## R.sub.1 is hydrogen, halogen or C.sub.1-C.sub.6alkyl; R.sub.2 is hydrogen, halogen, C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6alkenyl, C.sub.3-C.sub.6alkinyl, C.sub.3-C.sub.6cycloalkyl-C.sub.3-C.sub.6alkinyl, halophenoxy, halophenyl-C.sub.3-C.sub.6alkinyl, C(C.sub.1-C.sub.4alkyl)=NO-C.sub.1-C.sub.4alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6haloalkoxy, C.sub.2-C.sub.6haloalkenyl, or C.sub.2-C.sub.6haloalkenyloxy; R.sub.3 is hydrogen, halogen, C.sub.1-C.sub.6alkyl; R.sub.4, R.sub.5 and R.sub.6, independently from each other, are hydrogen, halogen or --R.sub.7; with the proviso that at least one of R.sub.4, R.sub.5 and R.sub.6 is different from hydrogen; R.sub.7 is hydrogen, C.sub.1-C.sub.6alkyl, C.sub.1-C.sub.6haloalkyl or C.sub.1-C.sub.4alkoxyalkyl; and R.sub.8 is hydrogen or methoxy; and agrochemically acceptable salts/isomers/structural isomers/stereoisomers/diastereoisomers/enantiomers/tautomers and N-oxides of those compounds; and component (B) is a compound selected from compounds known for their fungicidal and/or insecticidal activity, is particularly effective in controlling or preventing fungal diseases of useful plants.

DUAL INSECT REPELLENT POLYMER GELS

A composition comprising a first insect repellent compound, a second insect repellent compound, and a polymer that is miscible in the first insect repellent compound at 23 C. The polymer is dissolved in the first insect repellent compound. An example first insect repellent compound is N,N-diethyl-meta-toluamide, and example second insect repellent compounds are nootkatone, permethrin, or transfluthrin.