A reactive antibacterial compound is represented by formula (I) or (II): ##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 up to 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 formula (I) or (II): ##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 up to 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.

The present application relates to compositions comprising 4-chloroindole-3-acetic acid (4Cl-IAA) or an analogue thereof, or a combination of the latter, in the form of a potassium salt, a sodium salt or an amine salt. For example, such compositions can be used used in methods for selectively causing damage or mortality to weed.

The present application relates to compositions comprising 4-chloroindole-3-acetic acid (4Cl-IAA) or an analogue thereof, or a combination of the latter, in the form of a potassium salt, a sodium salt or an amine salt. For example, such compositions can be used used in methods for selectively causing damage or mortality to weed.

The present invention relates to active compound combinations, in particular within a fungicide composition, which comprises (A) a thiazolylisoxazoline of formula (I) and a further fungicidally active compound (B). Moreover, the invention relates to a method for curatively or preventively controlling the phytopathogenic fungi of plants or crops, to the use of a combination according to the invention for the treatment of seed, to a method for protecting a seed and not at least to the treated seed.

The present invention relates to active compound combinations, in particular within a fungicide composition, which comprises (A) a thiazolylisoxazoline of formula (I) and a further fungicidally active compound (B). Moreover, the invention relates to a method for curatively or preventively controlling the phytopathogenic fungi of plants or crops, to the use of a combination according to the invention for the treatment of seed, to a method for protecting a seed and not at least to the treated seed.

The invention disclosed herein is a synergistic plant growth stimulant composition comprising Melatonin and Nitrogenous compounds for improving plant growth, enhancing yield and decreasing the biotic-abiotic stresses on plants. The invention also disclosed herein is a process for preparation of said synergistic composition.

Compositions and methods for the disinfection of surfaces are provided. The compositions include at least about 40 weight percent of a C.sub.1-6 alcohol, and a primary enhancer selected from protein denaturants. The disinfectant composition is characterized by a pH of less than about 3. Broad spectrum efficacy is achieved, and synergistic activity is exhibited against C. difficile spores.

Compositions and methods for the disinfection of surfaces are provided. The compositions include at least about 40 weight percent of a C.sub.1-6 alcohol, and a primary enhancer selected from protein denaturants. The disinfectant composition is characterized by a pH of less than about 3. Broad spectrum efficacy is achieved, and synergistic activity is exhibited against C. difficile spores.

Antimicrobial compositions including at least one acid and at least one anionic surfactant are provided. In particular, food contact antimicrobial compositions including at least one acid and at least one anionic surfactant provide efficacious virucidal activity, including against Norovirus, having acceptable use solution pH that do not require use of personal protective equipment (PPE), are surface compatible and do not leave residues on treated surfaces. Methods of cleaning a surface with the compositions are also provided and may beneficially eliminate the need to rinse the antimicrobial compositions after use.