Provided is a pest control composition containing a novel iminopyridine derivative and other pest control agents.

Provided is a pest control composition containing an iminopyridine derivative represented by the following Formula (I) and at least one of other pest control agents:

##STR00001## [in the formula (I), Ar represents a 5- to 6-membered heterocycle which may be substituted, A represents a heterocycle having a 5- to 10-membered unsaturated bond including one or more nitrogen atoms, and has an imino group substituted with an R group at a position adjacent to the nitrogen atom present on the cycle, Y represents hydrogen, halogen and the like, and R represents any one of groups represented by the following Formulae (a) to (e), (y) or (z)].

##STR00002##

Compositions comprising miscible blends of antimicrobial bisguanide compounds with certain thermoplastic polymers are provided. These antimicrobial polymeric materials may be further processed into particulate or fiber form for use in fluid treatment devices and processes. The antimicrobial bisguanide compound, such as chlorhexidine, is distributed at the molecular level within at least one thermoplastic polymer, such as a polyolefin, in which the antimicrobial bisguanide compound is soluble to form a miscible blend, which may be from about 1% to about 25% by weight antimicrobial bisguanide compound. The antimicrobial polymeric materials may be secured in a device for antimicrobial treatment of a fluid. The devices may comprise a housing having at least one inlet orifice and at least one outlet orifice, the antimicrobial polymeric material being secured within the house and configured to contact a fluid flowing through the housing between the inlet orifice and the outlet orifice.

An ophthalmically compatible solution includes (a) about 0.005 to about 2 wt. %, based on the total weight of the ophthalmically compatible solution, of hyaluronic acid or a salt thereof; (b) about 0.01 to about 1 wt. %, based on the total weight of the ophthalmically compatible solution, of erythritol; (c) sodium chloride, potassium chloride or any combination thereof; and (d) one or more buffers.

An ophthalmically compatible solution includes (a) about 0.005 to about 2 wt. %, based on the total weight of the ophthalmically compatible solution, of hyaluronic acid or a salt thereof; (b) about 0.01 to about 1 wt. %, based on the total weight of the ophthalmically compatible solution, of erythritol; (c) sodium chloride, potassium chloride or any combination thereof; and (d) one or more buffers.

The disclosure relates to systems, compositions and methods for providing nutrients, root proliferants, crop protection agents and other crop inputs for a plant. The disclosure also relates to methods for increasing the uptake of a crop active compound into a growing plant.

The disclosure relates to systems, compositions and methods for providing nutrients, root proliferants, crop protection agents and other crop inputs for a plant. The disclosure also relates to methods for increasing the uptake of a crop active compound into a growing plant.

The present invention relates to halogen-substituted phenoxyphenylamidines of the general formula (I), to a process for their preparation, to the use of the amidines according to the invention for controlling unwanted microorganisms and also to an agrochemical formulation for this purpose, comprising the halogen-substituted phenoxyphenylamidines according to the invention. Furthermore, the invention relates to a method for controlling unwanted microorganisms by applying the compounds according to the invention to the microorganisms and/or their habitat.

The present invention relates to halogen-substituted phenoxyphenylamidines of the general formula (I), to a process for their preparation, to the use of the amidines according to the invention for controlling unwanted microorganisms and also to an agrochemical formulation for this purpose, comprising the halogen-substituted phenoxyphenylamidines according to the invention. Furthermore, the invention relates to a method for controlling unwanted microorganisms by applying the compounds according to the invention to the microorganisms and/or their habitat.

To provide a novel pesticidal composition, particularly a composition for a fungicide. A fungicidal or bactericidal composition comprising one or more compounds selected from oxime-substituted amide compounds represented by the formula (I), or their N-oxides or salts, and one or more compounds selected from known fungicidal or bactericidal compounds: ##STR00001##
wherein G.sup.1 represents a structure of G.sup.1-1, G.sup.1-27, etc., G.sup.2 represents a structure of G.sup.2-2, etc., W represents an oxygen atom, etc., X.sup.1 represents difluoromethyl, trifluoromethyl, etc., X.sup.2, X.sup.3, X.sup.4 and X.sup.5 each independently represents a hydrogen atom, etc., Y.sup.1 represents a halogen atom, etc., Y.sup.2 represents a hydrogen atom, a halogen atom, etc., Y.sup.3 represents a halogen atom, trifluoromethyl, C.sub.2-C.sub.6 alkynyl, etc., Y.sup.4 represents a hydrogen atom, etc., R.sup.1 represents C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.4 haloalkyl, etc., R.sup.2 and R.sup.3 each independently represents a hydrogen atom, methyl, etc., R.sup.4 represents a hydrogen atom, etc., and R.sup.5 represents methyl, etc.

To provide a novel pesticidal composition, particularly a composition for a fungicide. A fungicidal or bactericidal composition comprising one or more compounds selected from oxime-substituted amide compounds represented by the formula (I), or their N-oxides or salts, and one or more compounds selected from known fungicidal or bactericidal compounds: ##STR00001##
wherein G.sup.1 represents a structure of G.sup.1-1, G.sup.1-27, etc., G.sup.2 represents a structure of G.sup.2-2, etc., W represents an oxygen atom, etc., X.sup.1 represents difluoromethyl, trifluoromethyl, etc., X.sup.2, X.sup.3, X.sup.4 and X.sup.5 each independently represents a hydrogen atom, etc., Y.sup.1 represents a halogen atom, etc., Y.sup.2 represents a hydrogen atom, a halogen atom, etc., Y.sup.3 represents a halogen atom, trifluoromethyl, C.sub.2-C.sub.6 alkynyl, etc., Y.sup.4 represents a hydrogen atom, etc., R.sup.1 represents C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.4 haloalkyl, etc., R.sup.2 and R.sup.3 each independently represents a hydrogen atom, methyl, etc., R.sup.4 represents a hydrogen atom, etc., and R.sup.5 represents methyl, etc.