Patent classifications
A01N31/04
Formulation for promoting targeted pollination of pear tree crops in honey bees
A formulation and a composition that comprises it for promoting the pollination of pear crops (Pyrus) by biasing the foraging preferences of the honey bee (Apis mellifera). The formulation comprises the compounds limonene, linalool and α-pinene. Additionally, a method for targeting the bees' pollination activity towards the pear crops by using the formulation comprising the compounds limonene, linalool and α-pinene.
COMPOSITION BIOLOGICALLY ACTIVE TO STENOMA CATENIFER AND SUSTAINED RELEASE PREPARATION COMPRISING THE SAME FOR CONTROLLING INSECT PEST
There are provided a composition which has a larger attracted number than (9Z)-9,13-tetradecadien-11-ynal alone; and others. More specifically, there are provided a composition bioactive to Stenoma catenifer (STENCA), the composition including (9Z)-9,13-tetradecadien-11-ynal and (9E)-9,13-tetradecadien-11-ynal; a sustained release preparation for controlling STENCA, the preparation including the composition and a carrier or container for sustainedly releasing the (9Z)-9,13-tetradecadien-11-ynal and the (9E)-9,13-tetradecadien-11-ynal; and a method for controlling STENCA, the method including a step of installing the sustained release preparation in a field to release the (9Z)-9,13-tetradecadien-11-ynal and the (9E)-9,13-tetradecadien-11-ynal into the field.
COMPOSITION BIOLOGICALLY ACTIVE TO STENOMA CATENIFER AND SUSTAINED RELEASE PREPARATION COMPRISING THE SAME FOR CONTROLLING INSECT PEST
There are provided a composition which has a larger attracted number than (9Z)-9,13-tetradecadien-11-ynal alone; and others. More specifically, there are provided a composition bioactive to Stenoma catenifer (STENCA), the composition including (9Z)-9,13-tetradecadien-11-ynal and (9E)-9,13-tetradecadien-11-ynal; a sustained release preparation for controlling STENCA, the preparation including the composition and a carrier or container for sustainedly releasing the (9Z)-9,13-tetradecadien-11-ynal and the (9E)-9,13-tetradecadien-11-ynal; and a method for controlling STENCA, the method including a step of installing the sustained release preparation in a field to release the (9Z)-9,13-tetradecadien-11-ynal and the (9E)-9,13-tetradecadien-11-ynal into the field.
COMPOUNDS AND METHODS FOR PROMOTING PLANT GROWTH
Disclosed herein are compounds and methods for promoting plant growth. Formulations containing one or more disclosed compounds or salts thereof, and one or more excipients are disclosed. The formulation adjuvant can be a solid carrier, a liquid carrier, or a surface-active agent. Methods for promoting plant growth typically includes applying one or more formulations to a plant, a plant part, or a growing site of plant. The plant can be a cereal, grain, or vegetable plant. The plant part can be seed or seedling of a plant. The growing site of plant can be soil before, during, or after the plant is planted or a growing medium. In some embodiments, the one or more compounds or salts thereof in the one or more formulations are in an effective amount to decrease biosynthesis and release of strigolactone plant hormones from the plant.
COMPOUNDS AND METHODS FOR PROMOTING PLANT GROWTH
Disclosed herein are compounds and methods for promoting plant growth. Formulations containing one or more disclosed compounds or salts thereof, and one or more excipients are disclosed. The formulation adjuvant can be a solid carrier, a liquid carrier, or a surface-active agent. Methods for promoting plant growth typically includes applying one or more formulations to a plant, a plant part, or a growing site of plant. The plant can be a cereal, grain, or vegetable plant. The plant part can be seed or seedling of a plant. The growing site of plant can be soil before, during, or after the plant is planted or a growing medium. In some embodiments, the one or more compounds or salts thereof in the one or more formulations are in an effective amount to decrease biosynthesis and release of strigolactone plant hormones from the plant.
PEROXYGEN-BASED SKIN DISINFECTANTS EFFECTIVE AGAINST MYCOBACTERIA AND YEASTS
An aqueous skin-compatible antimicrobial solution effective against yeasts and mycobacteria, comprises 2-3.8 wt % of at least one peroxygen; from 1.5 up to 7 wt % of at least one aromatic monohydroxy alcohol selected from phenoxyethanol, phenethyl alcohol, cyclopentylmethanol, cyclohexylmethanol, benzyl alcohol, or any mixture thereof; from 0.5 up to 5 wt % of at least one high foaming amine oxide amphoteric surfactant; from 2 up to 10 wt % of at least one polyol-based skin conditioning agent; an effective amount of at least one pH adjusting agent for adjusting the solution pH to 2-3. The solution has a redox potential value from 220 to 280 mV, is readily biodegradable, and is free of aromatic carboxylic acids, inorganic salts, quaternary ammonium compounds, volatile aliphatic monohydroxy alcohols, other volatile organic compounds, halogen containing compounds, and other antimicrobial agents.
PEROXYGEN-BASED SKIN DISINFECTANTS EFFECTIVE AGAINST MYCOBACTERIA AND YEASTS
An aqueous skin-compatible antimicrobial solution effective against yeasts and mycobacteria, comprises 2-3.8 wt % of at least one peroxygen; from 1.5 up to 7 wt % of at least one aromatic monohydroxy alcohol selected from phenoxyethanol, phenethyl alcohol, cyclopentylmethanol, cyclohexylmethanol, benzyl alcohol, or any mixture thereof; from 0.5 up to 5 wt % of at least one high foaming amine oxide amphoteric surfactant; from 2 up to 10 wt % of at least one polyol-based skin conditioning agent; an effective amount of at least one pH adjusting agent for adjusting the solution pH to 2-3. The solution has a redox potential value from 220 to 280 mV, is readily biodegradable, and is free of aromatic carboxylic acids, inorganic salts, quaternary ammonium compounds, volatile aliphatic monohydroxy alcohols, other volatile organic compounds, halogen containing compounds, and other antimicrobial agents.
ANTIMICROBIAL COMPOSITIONS CONTAINING PEROXYPHTHALIC ACID AND/OR SALT THEREOF
Environmentally-friendly, surface-compatible, non-malodorous, sporicidal compositions, in solid or liquid form, containing a peroxyphthalic acid and/or salt thereof in combination with a synergistic additive selected from one or more of the groups consisting of (i) formic acid, acetic acid, benzoic acid, diglycolic acid, furoic acid, glycolic acid, lactic acid, mandelic acid, phenylacetic acid, sulfamic acid, sulfosuccinic acid, and salts thereof; (ii) C6-C24 alkyl or aryl ether carboxylic acids and their salts, C8-C24 alkyl taurines and their salts, aryl taurines and their salts, alkoxylated C8-C24 alkyl phosphoric acid esters and their salts, and glycerol ethers; (iii) aromatic alcohols, C2-C8 linear or branched alcohols, dibasic esters, 2-pyrrolidone, butyl carbitol, butyl cellosolve, lactate esters, butyl-3-hydroxybutyrate, and triacetin; and (iv) antimicrobial metals. Aqueous embodiments have a pH of less than 6. Kits and methods of antimicrobial reduction relating to same are also disclosed.
ANTIMICROBIAL COMPOSITIONS CONTAINING PEROXYPHTHALIC ACID AND/OR SALT THEREOF
Environmentally-friendly, surface-compatible, non-malodorous, sporicidal compositions, in solid or liquid form, containing a peroxyphthalic acid and/or salt thereof in combination with a synergistic additive selected from one or more of the groups consisting of (i) formic acid, acetic acid, benzoic acid, diglycolic acid, furoic acid, glycolic acid, lactic acid, mandelic acid, phenylacetic acid, sulfamic acid, sulfosuccinic acid, and salts thereof; (ii) C6-C24 alkyl or aryl ether carboxylic acids and their salts, C8-C24 alkyl taurines and their salts, aryl taurines and their salts, alkoxylated C8-C24 alkyl phosphoric acid esters and their salts, and glycerol ethers; (iii) aromatic alcohols, C2-C8 linear or branched alcohols, dibasic esters, 2-pyrrolidone, butyl carbitol, butyl cellosolve, lactate esters, butyl-3-hydroxybutyrate, and triacetin; and (iv) antimicrobial metals. Aqueous embodiments have a pH of less than 6. Kits and methods of antimicrobial reduction relating to same are also disclosed.
BIOFILM TREATMENT AGENT AND BIOFILM TREATMENT METHOD
[Problem] A treatment agent having an excellent ability to remove biofilms and a biofilm treatment method in which the treatment agent is used are provided.
[Solution] A biofilm treatment agent characterized by containing at least A1 and/or A2 below. A1: An aromatic monohydric alcohol. A2: An anthranilic acid analog and a biosurfactant. Preferably, the biofilm treatment agent is characterized by containing at least an aromatic monohydric alcohol, an anthranilic acid analog, a biosurfactant, and a synthetic surfactant.