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.

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.

A fungicidal or bactericidal composition containing an active ingredient A of an oxime-substituted amide compound represented by the formula (I), or its N-oxide or its salt, and an active ingredient (B) as a fungicidal or bactericidal compound:

##STR00001##

where in the formula (I), G.sup.1 is a structure of the following G.sup.1-1, G.sup.1-2, G.sup.1-3, G.sup.1-4, G.sup.1-5, G.sup.1-6, G.sup.1-7, G.sup.1-8 or G.sup.1-9, G.sup.2 is a structure of the following G.sup.2-1 or G.sup.2-2, W is an oxygen atom or a sulfur atom, R.sup.1 is C.sub.1-C.sub.6 alkyl, halo (C.sub.1-C.sub.4) alkyl, (C.sub.1-C.sub.4) alkyl substituted by R.sup.10, C.sub.3-C.sub.6 cycloalkyl, C.sub.3-C.sub.6 alkenyl, halo (C.sub.3-C.sub.4) alkenyl, C.sub.3-C.sub.6 alkynyl or phenyl, R.sup.2 is a hydrogen atom, methyl or ethyl, provided that R.sup.2 is methyl or ethyl when G.sup.1 is a structure of G.sup.1-1, X.sup.1 is a chlorine atom, X.sup.2, X.sup.3 and X.sup.5 each is a hydrogen atom, X.sup.4 is a hydrogen atom or a chlorine atom, and G.sup.2 is a structure of G.sup.2-1, Y.sup.3 is a chlorine atom, Y.sup.1, Y.sup.2, Y.sup.4 and Y.sup.5 each is a hydrogen atom, R.sup.3 is a hydrogen atom or methyl, or R.sup.2 and R.sup.3 may together form a cyclopropyl ring, R.sup.4 is a hydrogen atom, halo (C.sub.1-C.sub.4) alkylthio, C.sub.1-C.sub.4 alkylcarbonyl or C.sub.1-C.sub.4 alkoxycarbonyl.

A fungicidal or bactericidal composition containing an active ingredient A of an oxime-substituted amide compound represented by the formula (I), or its N-oxide or its salt, and an active ingredient (B) as a fungicidal or bactericidal compound:

##STR00001##

where in the formula (I), G.sup.1 is a structure of the following G.sup.1-1, G.sup.1-2, G.sup.1-3, G.sup.1-4, G.sup.1-5, G.sup.1-6, G.sup.1-7, G.sup.1-8 or G.sup.1-9, G.sup.2 is a structure of the following G.sup.2-1 or G.sup.2-2, W is an oxygen atom or a sulfur atom, R.sup.1 is C.sub.1-C.sub.6 alkyl, halo (C.sub.1-C.sub.4) alkyl, (C.sub.1-C.sub.4) alkyl substituted by R.sup.10, C.sub.3-C.sub.6 cycloalkyl, C.sub.3-C.sub.6 alkenyl, halo (C.sub.3-C.sub.4) alkenyl, C.sub.3-C.sub.6 alkynyl or phenyl, R.sup.2 is a hydrogen atom, methyl or ethyl, provided that R.sup.2 is methyl or ethyl when G.sup.1 is a structure of G.sup.1-1, X.sup.1 is a chlorine atom, X.sup.2, X.sup.3 and X.sup.5 each is a hydrogen atom, X.sup.4 is a hydrogen atom or a chlorine atom, and G.sup.2 is a structure of G.sup.2-1, Y.sup.3 is a chlorine atom, Y.sup.1, Y.sup.2, Y.sup.4 and Y.sup.5 each is a hydrogen atom, R.sup.3 is a hydrogen atom or methyl, or R.sup.2 and R.sup.3 may together form a cyclopropyl ring, R.sup.4 is a hydrogen atom, halo (C.sub.1-C.sub.4) alkylthio, C.sub.1-C.sub.4 alkylcarbonyl or C.sub.1-C.sub.4 alkoxycarbonyl.

The invention relates to quaternary ammonium multi-dentate mono-, bis-, tris- and tetrakis-phosphonate compounds, processes for preparing quaternary ammonium multi-dentate mono-, bis-, tris- and tetrakis-phosphonate compounds, antimicrobial coating compositions comprising quaternary ammonium multi-dentate mono-, bis-, tris- and tetrakis-phosphonate compounds and method of treating a surface with said compositions to provide a durable, antimicrobial-treated surface.

The invention relates to quaternary ammonium multi-dentate mono-, bis-, tris- and tetrakis-phosphonate compounds, processes for preparing quaternary ammonium multi-dentate mono-, bis-, tris- and tetrakis-phosphonate compounds, antimicrobial coating compositions comprising quaternary ammonium multi-dentate mono-, bis-, tris- and tetrakis-phosphonate compounds and method of treating a surface with said compositions to provide a durable, antimicrobial-treated surface.

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.

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.

The present invention relates to a pesticide composition intended for protecting plants, crops or seeds against fungal diseases or insect damages, and the corresponding methods of protection by application of the said composition. More precisely, the subject of the present invention is a pesticide composition based on a tetrazolyloxime derivative and a fungicide or an insecticide active substance or compound.

The present invention relates to a pesticide composition intended for protecting plants, crops or seeds against fungal diseases or insect damages, and the corresponding methods of protection by application of the said composition. More precisely, the subject of the present invention is a pesticide composition based on a tetrazolyloxime derivative and a fungicide or an insecticide active substance or compound.