A01P7/04

A STABLE, SOLVENT-FREE, SELF-EMULSIFIABLE CONCENTRATE
20230232821 · 2023-07-27 ·

Disclosed herein is a stable, solvent free, self emulsifiable concentrate including a biocide and an ethoxylated fatty acid alkyl ester of formula (I). Additionally disclosed herein is a method of forming the stable, solvent free, self emulsifiable concentrate. Additionally disclosed herein is a kit for preparing the concentrate, including as separate components a biocide and an ethoxylated fatty acid alkyl ester of formula (I). Further disclosed herein is a method of using the concentrate for the treatment of plants and soil, lawns and gardens, and buildings and other surfaces and structures where pests reside.

A STABLE, SOLVENT-FREE, SELF-EMULSIFIABLE CONCENTRATE
20230232821 · 2023-07-27 ·

Disclosed herein is a stable, solvent free, self emulsifiable concentrate including a biocide and an ethoxylated fatty acid alkyl ester of formula (I). Additionally disclosed herein is a method of forming the stable, solvent free, self emulsifiable concentrate. Additionally disclosed herein is a kit for preparing the concentrate, including as separate components a biocide and an ethoxylated fatty acid alkyl ester of formula (I). Further disclosed herein is a method of using the concentrate for the treatment of plants and soil, lawns and gardens, and buildings and other surfaces and structures where pests reside.

INSECTICIDAL PROTEINS AND METHODS FOR THEIR USE

Compositions and methods for controlling pests are provided. The methods involve transforming organisms with a nucleic acid sequence encoding an insecticidal protein. In particular, the nucleic acid sequences are useful for preparing plants and microorganisms that possess insecticidal activity. Thus, transformed bacteria, plants, plant cells, plant tissues and seeds are provided. Compositions are insecticidal nucleic acids and proteins of bacterial species. The sequences find use in the construction of expression vectors for subsequent transformation into organisms of interest including plants, as probes for the isolation of other homologous (or partially homologous) genes. The pesticidal proteins find use in controlling, inhibiting growth or killing Hemipteran, Lepidopteran, Coleopteran, Dipteran, fungal, and nematode pest populations and for producing compositions with insecticidal activity.

EMBEDDED HIGH-MOLECULAR-WEIGHT COMPOSITIONS

A method for embedding a first component in a high molecular weight second component is disclosed. Embedded high-molecular-weight compositions are also disclosed.

DIAMIDE SUSPENSION CONCENTRATE COMPOSITIONS

Described herein are suspension concentration (SC) formulations comprising a diamide pesticide in high strength. The present formulations show excellent stability and dispersibility in water, as well as low air entrapment.

DIAMIDE SUSPENSION CONCENTRATE COMPOSITIONS

Described herein are suspension concentration (SC) formulations comprising a diamide pesticide in high strength. The present formulations show excellent stability and dispersibility in water, as well as low air entrapment.

FLEA AND TICK COLLAR
20230028884 · 2023-01-26 · ·

The disclosure provides an insecticide formulation, comprising: i) a neonicotinoid optionally together with a pyrethroid; ii) an insect growth regulator; and iii) a filling agent together with a plasticizer.

Methods and Compositions for Use in Glued-Wood Products

The present invention relates to biocide-composites providing high retention of biocides in glueline-treated glued-wood products that are hot-pressed or hot-pressed and block-stacked during manufacture.

Methods and Compositions for Use in Glued-Wood Products

The present invention relates to biocide-composites providing high retention of biocides in glueline-treated glued-wood products that are hot-pressed or hot-pressed and block-stacked during manufacture.

3-N-CYCLOPROPYLMETHYL-2-FLUOROBENZAMIDE COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF
20230020373 · 2023-01-19 ·

Disclosed are a 3-N-cyclopropylmethyl-2-fluorobenzamide compound, a preparation method therefor and the use thereof. The compound has a structure as represented by the following formula I. This compound can be used for the preparation of an m-diamide compound substituted with a 3-N-cyclopropylmethyl derivative. The m-diamide compound substituted with the 3-N-cyclopropylmethyl derivative, when serving as an insecticide, has the characteristics of a good fast-acting property, needing to use a low amount thereof, and being more beneficial for environmental protection. The 3-N-cyclopropylmethyl-2-fluorobenzamide compound is easy to synthesize and has mild conditions, and when used for preparing a m-diamide compound insecticide substituted with a 3-N-cyclopropylmethyl derivative, same is easy to synthesize and has a low synthesis cost and a high yield.