A01P3/00

MULTIPURPOSE PRODUCT WITH PROLONGED ANTIMICROBIAL ACTION AND METHOD OF PRODUCING

Multipurpose product with prolonged antimicrobial action comprising at least one quaternary ammonium and copper nanoparticles in non-oxidized metallic state (Cu.sup.0), where copper nanoparticles in non-oxidized metallic state (Cu.sup.0) are found nucleated in at least one quaternary ammonium. A method for producing a multipurpose product with prolonged antimicrobial action.

PROTECTIVE HEMP OIL FOR WOOD TREATMENT METHOD
20230044862 · 2023-02-09 ·

A protectant and sealant solution and method of use thereof, configured to protect wood from premature decay when disposed in contact with the earth. The solution is composed of processed hemp oil which is mixed with bio-diesel and other oils to form the protectant solution. The wood is then impregnated with the solution via pressure treatment within a retort cylinder. The solution is configured to protect utility poles and other wooden construction members which are known for prolonged contact with soil. The solution is designed as a safe replacement for pentachlorophenol solutions which have been found to be harmful to the soil and water table.

LIQUID PESTICIDAL COMPOSITION
20230011898 · 2023-01-12 · ·

Provided herein is a liquid pesticidal composition, comprising: (a) 3 to 10 mass% of a pesticidal active ingredient having a water solubility at 25° C. of 15 mass ppm or less and a melting point of 10° C. or more; (b) 3.6 to 60 mass% of a first solvent that is ε-caprolactone; (c) 19.5 to 85 mass% of a second solvent having a water solubility at 25° C. of 1 mass% or less; and (d) 1 to 30 mass% of a surfactant, wherein a total content of the pesticidal active ingredient, the first solvent, the second solvent, and the surfactant is 60 mass% or more, a content of the first solvent relative to a content of the pesticidal active ingredient is from 1.2 to 15.0 times by mass, and a content of the second solvent relative to the content of the pesticidal active ingredient is from 6.5 to 25.0 times by mass.

AZABICYCLYL-SUBSTITUTED HETEROCYCLES AS FUNGICIDES

The present disclosure relates to azabicyclyl-substituted heterocyclic compounds of formula (I), wherein A.sup.1, A.sup.2, m, R.sup.3, R.sup.4, R.sup.5, L, R.sup.6, T, the ring Y, p, R.sup.7 and Q have the meanings as defined in the specification, to compositions comprising such compounds, to processes and intermediates for their preparation as well as the uses thereof for controlling phytopathogenic microorganisms, such as phytopathogenic fungi.

##STR00001##

AZABICYCLYL-SUBSTITUTED HETEROCYCLES AS FUNGICIDES

The present disclosure relates to azabicyclyl-substituted heterocyclic compounds of formula (I), wherein A.sup.1, A.sup.2, m, R.sup.3, R.sup.4, R.sup.5, L, R.sup.6, T, the ring Y, p, R.sup.7 and Q have the meanings as defined in the specification, to compositions comprising such compounds, to processes and intermediates for their preparation as well as the uses thereof for controlling phytopathogenic microorganisms, such as phytopathogenic fungi.

##STR00001##

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.

MICROBIOCIDAL DERIVATIVES

Compounds of the formula (I) wherein the substituents are as defined in claim 1, useful as pesticides, and especially fungicides.

##STR00001##

MICROBIOCIDAL DERIVATIVES

Compounds of the formula (I) wherein the substituents are as defined in claim 1, useful as pesticides, and especially fungicides.

##STR00001##

PHYTOSANITARY AGENT AND ITS PARTICULAR USE IN THE TREATMENT OF PLANTS INFECTED BY XYLELLA FASTIDIOSA
20230000077 · 2023-01-05 ·

The invention relates to the use of an organometallic coordination complex or its phytopharmaceutically acceptable salt of a M.sup.m+ metal and of at least one L ligand, where M.sup.m+ is a transition metal having an oxidation number m, L is a ligand of general formula (VII) or its anion, wherein R.sup.1 is selected from the group consisting of oxygen, mono or polycyclic alkyl, naphthalene residue, anthracene residue and their hydroxylated or ketone derivatives; R.sup.2 and R.sup.3 are identical or different and are selected independently of each other from hydrogen, halogen, a hydroxyl group, an alkoxy group, a linear or branched alkyl group, a cycloalkyl group or R.sup.2 and R.sup.3 together forming a benzene derivative; R.sup.6, R.sup.7 and R.sup.8 are identical or different and independently of each other are selected from hydrogen, a hydroxyl group, an alkoxy group, a linear or branched alkyl group, a cycloalkyl group, a phenyl group, an aryl group in the treatment of Xylella fastidiosa in a plant. The invention also concerns the use of the compound of formula (VII) in the treatment of Xylella fastidiosa in a plant, also in combination with the organometallic coordination complex. Advantageously, the invention concerns the treatment of olive trees.