A01N57/12

Antimicrobial composition comprising thymol, terpineol and a cationic phospholipid

The present invention relates to an antimicrobial composition and more particularly an antimicrobial composition for leave-on applications. The present invention discloses an antimicrobial composition comprising; a) 0.01 to 2% by weight of thymol; b) 0.01 to 2% by weight of terpineol; and c) 0.1 to 2% by weight of a cationic phospholipid complex.

Antimicrobial composition comprising thymol, terpineol and a cationic phospholipid

The present invention relates to an antimicrobial composition and more particularly an antimicrobial composition for leave-on applications. The present invention discloses an antimicrobial composition comprising; a) 0.01 to 2% by weight of thymol; b) 0.01 to 2% by weight of terpineol; and c) 0.1 to 2% by weight of a cationic phospholipid complex.

Antimicrobial composition comprising thymol, terpineol and a cationic phospholipid

The present invention relates to an antimicrobial composition and more particularly an antimicrobial composition for leave-on applications. The present invention discloses an antimicrobial composition comprising; a) 0.01 to 2% by weight of thymol; b) 0.01 to 2% by weight of terpineol; and c) 0.1 to 2% by weight of a cationic phospholipid complex.

AGROCHEMICAL ELECTROLYTE COMPOSITIONS
20200128819 · 2020-04-30 · ·

An agrochemical concentrate comprises lecithin and at least one agrochemical active. The agrochemical concentrate may also comprise a dispersant selected from sucrose ester, alkylpolyglucoside, alkylnaphthalene sulphonates, phosphate ester, sorbitol ester, polyglycerol ester, alkyl sulphates, sodium lauryl sulphate, alkylglucamides, and dialkyl sulphosuccinates. An aqueous formulation comprises a dilution of the agrochemical concentrate in an electrolyte. A pre-blend comprises lecithin and a dispersant. A method of preparing the agrochemical concentrate and a method for treating vegetation are also disclosed.

INSECT CONTROL DEVICE AND METHOD FOR HOUSEHOLD OUTDOOR GARBAGE RECEPTACLES
20200128809 · 2020-04-30 · ·

An insect control device is provided for controlling insects in a household garbage receptacle used in an outdoor or semi-outdoor environment. The insect control device includes an outer housing with gas-flow apertures therein, a quantity of a gas-releasing insect poison contained within the housing, and an adhesive attaching element for securing the housing to an inner surface of a closed or lidded household garbage receptacle. Gas released by the insect poison flows out of the housing through the gas-flow apertures to permeate the air inside the enclosed garbage containment area and kill insects therein while the adhesive element keeps the device securely in place within the garbage receptacle and out of the reach of children and pets during both use and emptying of the receptacle.

Formulations for killing biting arthropods
10631536 · 2020-04-28 · ·

Killing one or more biting arthropods selected from the group consisting of mosquitoes, bed bugs and ticks is accomplished by bringing the biting arthropods into contact with a toxic amount of a formulation comprising: (1) one or more compounds of structure (I), wherein the compounds of structure (I) comprise: ##STR00001##
wherein R is selected from the group consisting of OH, O, OC(O)R.sub.4, OR.sub.6, (OR.sub.6).sub.2, wherein each R.sub.6 is independently selected from an alkyl group containing from 1 to 4 carbon atoms and R.sub.4 is a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to two double bonds and from 1 to 15 carbon atoms: X is O or CH.sub.2, with the proviso that when X is O, then R can only be O; each Z is independently selected from the group consisting of (CH) and (CH.sub.2); y is a numeral selected from 1 and 2; R.sub.1 is selected from the group consisting of H or a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to two double bonds and from 1 to 15 carbon atoms; R.sub.2 is selected from the group consisting of H and a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to three double bonds and from 1 to 15 carbon atoms; R.sub.3 is selected from the group consisting of H and a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to three double bonds and from 1 to 15 carbon atoms, (CH.sub.2).sub.nOH, C(O)OR.sub.5, CH.sub.2C(O)OR.sub.7, CH.sub.2C(O)R.sub.8, C(O)NR.sub.9R.sub.10, CH.sub.2C(O)NR.sub.11R.sub.12 where each of R.sub.5, R.sub.7, R.sub.8, R.sub.9, R.sub.10, R.sub.11 and R.sub.12 is independently selected from H and a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to three double bonds and from 1 to 15 carbon atoms and n is an integer of from 1 to 12; the bond between the 2 and 3 positions in the ring structure may be a single or a double bond; and wherein the compounds of structure (I) contain from 11 to 20 total carbon atoms; and (2) one or more toxicant compounds selected from the group consisting of pyrethroids, carbamates, and organophosphates. The formulation can be a synergistic formulation.

Formulations for killing biting arthropods
10631536 · 2020-04-28 · ·

Killing one or more biting arthropods selected from the group consisting of mosquitoes, bed bugs and ticks is accomplished by bringing the biting arthropods into contact with a toxic amount of a formulation comprising: (1) one or more compounds of structure (I), wherein the compounds of structure (I) comprise: ##STR00001##
wherein R is selected from the group consisting of OH, O, OC(O)R.sub.4, OR.sub.6, (OR.sub.6).sub.2, wherein each R.sub.6 is independently selected from an alkyl group containing from 1 to 4 carbon atoms and R.sub.4 is a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to two double bonds and from 1 to 15 carbon atoms: X is O or CH.sub.2, with the proviso that when X is O, then R can only be O; each Z is independently selected from the group consisting of (CH) and (CH.sub.2); y is a numeral selected from 1 and 2; R.sub.1 is selected from the group consisting of H or a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to two double bonds and from 1 to 15 carbon atoms; R.sub.2 is selected from the group consisting of H and a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to three double bonds and from 1 to 15 carbon atoms; R.sub.3 is selected from the group consisting of H and a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to three double bonds and from 1 to 15 carbon atoms, (CH.sub.2).sub.nOH, C(O)OR.sub.5, CH.sub.2C(O)OR.sub.7, CH.sub.2C(O)R.sub.8, C(O)NR.sub.9R.sub.10, CH.sub.2C(O)NR.sub.11R.sub.12 where each of R.sub.5, R.sub.7, R.sub.8, R.sub.9, R.sub.10, R.sub.11 and R.sub.12 is independently selected from H and a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to three double bonds and from 1 to 15 carbon atoms and n is an integer of from 1 to 12; the bond between the 2 and 3 positions in the ring structure may be a single or a double bond; and wherein the compounds of structure (I) contain from 11 to 20 total carbon atoms; and (2) one or more toxicant compounds selected from the group consisting of pyrethroids, carbamates, and organophosphates. The formulation can be a synergistic formulation.

Formulations for killing biting arthropods
10631536 · 2020-04-28 · ·

Killing one or more biting arthropods selected from the group consisting of mosquitoes, bed bugs and ticks is accomplished by bringing the biting arthropods into contact with a toxic amount of a formulation comprising: (1) one or more compounds of structure (I), wherein the compounds of structure (I) comprise: ##STR00001##
wherein R is selected from the group consisting of OH, O, OC(O)R.sub.4, OR.sub.6, (OR.sub.6).sub.2, wherein each R.sub.6 is independently selected from an alkyl group containing from 1 to 4 carbon atoms and R.sub.4 is a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to two double bonds and from 1 to 15 carbon atoms: X is O or CH.sub.2, with the proviso that when X is O, then R can only be O; each Z is independently selected from the group consisting of (CH) and (CH.sub.2); y is a numeral selected from 1 and 2; R.sub.1 is selected from the group consisting of H or a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to two double bonds and from 1 to 15 carbon atoms; R.sub.2 is selected from the group consisting of H and a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to three double bonds and from 1 to 15 carbon atoms; R.sub.3 is selected from the group consisting of H and a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to three double bonds and from 1 to 15 carbon atoms, (CH.sub.2).sub.nOH, C(O)OR.sub.5, CH.sub.2C(O)OR.sub.7, CH.sub.2C(O)R.sub.8, C(O)NR.sub.9R.sub.10, CH.sub.2C(O)NR.sub.11R.sub.12 where each of R.sub.5, R.sub.7, R.sub.8, R.sub.9, R.sub.10, R.sub.11 and R.sub.12 is independently selected from H and a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to three double bonds and from 1 to 15 carbon atoms and n is an integer of from 1 to 12; the bond between the 2 and 3 positions in the ring structure may be a single or a double bond; and wherein the compounds of structure (I) contain from 11 to 20 total carbon atoms; and (2) one or more toxicant compounds selected from the group consisting of pyrethroids, carbamates, and organophosphates. The formulation can be a synergistic formulation.

Reactive antibacterial compound and preparation method thereof
10609927 · 2020-04-07 · ·

A reactive antibacterial compound is represented by the general formula (I): ##STR00001##
wherein R.sub.1 represents OCN-L-NHCOOR, OCN-L-NHCONHR, OCN-L-NHCOSR, OCN-L-COOR, or OCN-L-COONHR. G1 represents OCN-M-NHCOOG, OCN-M-NHCONHG, OCN-M-NHCOSG, OCN-M-COOG, or OCN-M-COONHG. L, M, R and G independently for each occurrence represent divalent alkyl and cycloalkyl having from 1 to 18 carbon atoms, optionally substituted by up to 18 heteroatoms. R.sub.4 and G.sub.4 independently for each occurrence represent a divalent alkyl and cycloalkyl having from 1 to 18 carbon atoms, optionally substituted by at most 18 heteroatoms. G.sub.2 and G.sub.3 independently for each occurrence represent H, F, Cl, Br, I, OCH3, OCH2CH3, OPr, CN, SCN, NO, NO2, a monovalent unsubstituted or substituted alkyl, cycloalkyl, or aryl having from 1 to 7 carbon atoms. Z and X independently for each occurrence represent COO, SO3, or OPO2OR.sub.5. R.sub.5 represents a monovalent unsubstituted or substituted alkyl, cycloalkyl, or aryl having from 1 to 6 carbon atoms.

Reactive antibacterial compound and preparation method thereof
10609927 · 2020-04-07 · ·

A reactive antibacterial compound is represented by the general formula (I): ##STR00001##
wherein R.sub.1 represents OCN-L-NHCOOR, OCN-L-NHCONHR, OCN-L-NHCOSR, OCN-L-COOR, or OCN-L-COONHR. G1 represents OCN-M-NHCOOG, OCN-M-NHCONHG, OCN-M-NHCOSG, OCN-M-COOG, or OCN-M-COONHG. L, M, R and G independently for each occurrence represent divalent alkyl and cycloalkyl having from 1 to 18 carbon atoms, optionally substituted by up to 18 heteroatoms. R.sub.4 and G.sub.4 independently for each occurrence represent a divalent alkyl and cycloalkyl having from 1 to 18 carbon atoms, optionally substituted by at most 18 heteroatoms. G.sub.2 and G.sub.3 independently for each occurrence represent H, F, Cl, Br, I, OCH3, OCH2CH3, OPr, CN, SCN, NO, NO2, a monovalent unsubstituted or substituted alkyl, cycloalkyl, or aryl having from 1 to 7 carbon atoms. Z and X independently for each occurrence represent COO, SO3, or OPO2OR.sub.5. R.sub.5 represents a monovalent unsubstituted or substituted alkyl, cycloalkyl, or aryl having from 1 to 6 carbon atoms.