A01N57/34

1,7-diaryl-1,6-heptadiene-3,5-dione derivatives, methods for the production and use thereof

1,7-diaryl-1,6-heptadiene-3,5-dione derivatives, methods for the production and use thereof.

1,7-diaryl-1,6-heptadiene-3,5-dione derivatives, methods for the production and use thereof

1,7-diaryl-1,6-heptadiene-3,5-dione derivatives, methods for the production and use thereof.

ANTIMICROBIAL COMPOUNDS OR PRECURSORS THEREOF COMRPISING ONE OR MORE CATIONIC CENTERS AND A COATING-INCORPORATION GROUP

The present disclosure describes monomeric compounds and polymeric compounds that comprise at least one of the monomeric compounds and compositions that can be included in a coating composition for coating a substrate. The coated substrate may have biocidal activity or the potential for increased biocidal activity. The potential for increased biocidal activity may be realized by exposing the coated substrate to one or more further agents, such as one or more halogens. The monomer compound comprises (i) one or more cationic centers, (ii) an N-halamine precursor group, and (iii) at least one coating-incorporation group (CIG). The CIG bonds with another component within the coating composition or alternatively the CIG may bond with a component of the substrate. The CIG of the composition may incorporate the monomer into the coating composition, may incorporate the coating composition onto the substrate, or the CIG may perform both functions.

ANTIMICROBIAL COMPOUNDS OR PRECURSORS THEREOF COMRPISING ONE OR MORE CATIONIC CENTERS AND A COATING-INCORPORATION GROUP

The present disclosure describes monomeric compounds and polymeric compounds that comprise at least one of the monomeric compounds and compositions that can be included in a coating composition for coating a substrate. The coated substrate may have biocidal activity or the potential for increased biocidal activity. The potential for increased biocidal activity may be realized by exposing the coated substrate to one or more further agents, such as one or more halogens. The monomer compound comprises (i) one or more cationic centers, (ii) an N-halamine precursor group, and (iii) at least one coating-incorporation group (CIG). The CIG bonds with another component within the coating composition or alternatively the CIG may bond with a component of the substrate. The CIG of the composition may incorporate the monomer into the coating composition, may incorporate the coating composition onto the substrate, or the CIG may perform both functions.

Biocidal compositions

Embodiments of the present subject matter provide a biocidal composition comprising an aqueous mixture of (a) a phosphonium compound and (b) a polymeric ammonium compound, wherein the weight ratio of compound (a) to compound (b) is from 0.2:1 to 20:1, and wherein the phosphonium compound (a) has formula: ##STR00001## wherein each R is independently a C.sub.1-C.sub.6 alkyl group which is unsubstituted or substituted by a cyano, hydroxyl, esterified hydroxyl or aryl group; R.sup.1 represents a C.sub.8-C.sub.18 alkyl group which is substituted or unsubstituted; and X represents either chlorine or bromine; and wherein the polymeric ammonium compound (b) comprises the repeat unit: ##STR00002## wherein each R.sup.2 is independently a C.sub.1-C.sub.2 alkyl group which is substituted or unsubstituted; R.sup.3 represents a C.sub.2-C.sub.18 alkyl or alkenyl group which is substituted or unsubstituted; and R.sup.4 represents a C.sub.2-C.sub.18 alkyl or alkenyl group which is substituted or unsubstituted, a diethyl ether group, an isopropanol group, a N,N-dipropylurea group, or a 2-butene group. In some embodiments, the biocidal composition has a synergy index (SI) of less than 1 in relation to the effect of the composition on the inhibition of growth of biological organisms.

Biocidal compositions

Embodiments of the present subject matter provide a biocidal composition comprising an aqueous mixture of (a) a phosphonium compound and (b) a polymeric ammonium compound, wherein the weight ratio of compound (a) to compound (b) is from 0.2:1 to 20:1, and wherein the phosphonium compound (a) has formula: ##STR00001## wherein each R is independently a C.sub.1-C.sub.6 alkyl group which is unsubstituted or substituted by a cyano, hydroxyl, esterified hydroxyl or aryl group; R.sup.1 represents a C.sub.8-C.sub.18 alkyl group which is substituted or unsubstituted; and X represents either chlorine or bromine; and wherein the polymeric ammonium compound (b) comprises the repeat unit: ##STR00002## wherein each R.sup.2 is independently a C.sub.1-C.sub.2 alkyl group which is substituted or unsubstituted; R.sup.3 represents a C.sub.2-C.sub.18 alkyl or alkenyl group which is substituted or unsubstituted; and R.sup.4 represents a C.sub.2-C.sub.18 alkyl or alkenyl group which is substituted or unsubstituted, a diethyl ether group, an isopropanol group, a N,N-dipropylurea group, or a 2-butene group. In some embodiments, the biocidal composition has a synergy index (SI) of less than 1 in relation to the effect of the composition on the inhibition of growth of biological organisms.

Biocidal compositions

Embodiments of the present subject matter provide a biocidal composition comprising an aqueous mixture of (a) a phosphonium compound and (b) a polymeric ammonium compound, wherein the weight ratio of compound (a) to compound (b) is from 0.2:1 to 20:1, and wherein the phosphonium compound (a) has formula: ##STR00001## wherein each R is independently a C.sub.1-C.sub.6 alkyl group which is unsubstituted or substituted by a cyano, hydroxyl, esterified hydroxyl or aryl group; R.sup.1 represents a C.sub.8-C.sub.18 alkyl group which is substituted or unsubstituted; and X represents either chlorine or bromine; and wherein the polymeric ammonium compound (b) comprises the repeat unit: ##STR00002## wherein each R.sup.2 is independently a C.sub.1-C.sub.2 alkyl group which is substituted or unsubstituted; R.sup.3 represents a C.sub.2-C.sub.18 alkyl or alkenyl group which is substituted or unsubstituted; and R.sup.4 represents a C.sub.2-C.sub.18 alkyl or alkenyl group which is substituted or unsubstituted, a diethyl ether group, an isopropanol group, a N,N-dipropylurea group, or a 2-butene group. In some embodiments, the biocidal composition has a synergy index (SI) of less than 1 in relation to the effect of the composition on the inhibition of growth of biological organisms.

Growth enhancement of plant

Provided is a method to increase the growth of a plant by coating a seed of said plant with a composition comprising at least one of various cationic compounds; notably permitting to develop its biomass and reach its maturity. Provided also is a seed coating composition used in such a method.

Growth enhancement of plant

Provided is a method to increase the growth of a plant by coating a seed of said plant with a composition comprising at least one of various cationic compounds; notably permitting to develop its biomass and reach its maturity. Provided also is a seed coating composition used in such a method.

Methods for controlling depolymerization of polymer compositions

A method of controlling or arresting the rate of depolymerization of a polymer composition during a biocide treatment, and use of such methods in oilfield and industrial applications. Also disclosed are methods of preparing a visco-stable application fluid containing a biocide in an amount effective to reduce bacteria count, as well as additive compositions capable of reducing bacteria count in application fluids while maintaining viscosity in such fluids. Also disclosed are methods of preparing biocide-containing application fluids with improved friction reducing properties, as well as related compositions.