FUNGICIDAL COMPOSITIONS

Described herein are fungicidal compositions in the form of an emulsifiable concentrates that include a first fungicidal compound, optionally, at least one additional fungicidal compound, two or more surfactants and a water immiscible organic solvent comprised of a mixture of organic compounds including at least one acetate ester, at least one N,N-dialkylcarboxamide and at least one of a ketone and an alcohol, and methods of use of such compositions to control important fungal diseases of plants.

Skip to: Description  ·  Claims  · Patent History  ·  Patent History
Description
PRIORITY CLAIM

This application claims the benefit of U.S. Provisional Application No. 62/098,199, filed Dec. 30, 2014, U.S. Provisional Application No. 62/098,202, filed Dec. 30, 2014, and U.S. Provisional Application No. 62/098,224, filed Dec. 30, 2014, the complete disclosures of all of which are hereby expressly incorporated by reference.

FIELD OF THE INVENTION

Some aspects of the invention relate to methods of use of fungicides which are suitable for use in agriculture.

BACKGROUND AND SUMMARY

Liquid pre-mix concentrates comprising two or more active ingredients are useful in a wide variety of agricultural applications. For example, two or more pesticidal active ingredients may be combined in order to control a wider spectrum of pests, or to utilize multiple modes of action, compared to the individual active ingredients alone.

Water insoluble pesticide active ingredients may be formulated in water as aqueous suspension concentrates (SC) or by dissolving the water insoluble pesticide in an organic solvent and forming an emulsifiable concentrate (EC). The preparation of these liquid, pre-mix concentrates can be challenging owing to chemical and/or physical instability issues.

Emulsifiable concentrate formulations, also known as emulsion concentrates or ECs, are widely used in crop protection. The disadvantages of some emulsifiable concentrates include their poor cold temperature stability and the pronounced tendency of the active ingredient to crystallize, owing to the low solubility of some active ingredients in the concentrate. It was an object of the present disclosure to provide an emulsifiable concentrate which overcomes these disadvantages.

Provided herein is a fungicidal composition comprising: a) a fungicidal compound of the Formula

b) at least one ionic surfactant; c) at least one nonionic surfactant; d) an acetate ester; e) an N,N-dialkylcarboxamide; and f) at least one of a ketone and an alcohol.

In certain embodiments, the described fungicidal composition may include at least one additional fungicidal compound.

In certain embodiments, the at least one acetate ester, the at least one N,N-dialkylcarboxamide and the at least one of a ketone and an alcohol together form a water immiscible organic solvent for the described fungicidal composition.

In certain embodiments, the described fungicidal composition forms a stable, homogenous emulsifiable concentrate that readily emulsifies and forms a stable emulsion without crystallization of the fungicidal compound when added to water.

In certain embodiments, the described composition may include an adjuvant that improves the fungicidal performance of the composition.

In certain embodiments, the described composition may include additional active ingredients and/or inert formulation ingredients.

Also provided herein is a method of controlling plant derived fungal pathogens or diseases comprising contacting the vegetation or an area adjacent thereto to prevent the growth of the fungal pathogens or diseases with a fungicidally effective amount of a fungicidal composition comprising: a) a fungicidal compound of the Formula

b) at least one ionic surfactant; c) at least one nonionic surfactant; d) an acetate ester; e) an N,N-dialkylcarboxamide; and f) at least one of a ketone and an alcohol.

A first embodiment including methods of controlling fungal plant pathogens or diseases of plants comprising the steps of contacting the vegetation or an area adjacent thereto to prevent the growth of the fungal pathogens or diseases with a fungicidally effective amount of a fungicidal composition comprising: a) a fungicidal compound of the Formula

b) at least one ionic surfactant; c) at least one nonionic surfactant; d) at least one acetate ester; e) at least one N,N-dialkylcarboxamide; and f) at least one of a ketone and an alcohol.

A second embodiment including the method of the first embodiment, wherein the fungicidal composition includes from about 1 gram per liter (g/L) to about 200 g/L of the fungicidal compound of the Formula

A third embodiment including any of the methods of any of the first or the second embodiments, wherein the fungicidal composition includes from about 1 g/L to about 100 g/L of at least one ionic surfactant, wherein the at least one ionic surfactant includes at least one anionic surfactant.

A fourth embodiment including any of the methods of any of the first through the third embodiments, wherein the fungicidal composition includes from about 1 g/L to about 200 g/L of the at least one nonionic surfactant.

A fifth embodiment including any of the methods of first through the fourth embodiments, wherein the fungicidal composition includes from about 50 g/L to about 700 g/L of the at least one acetate ester.

A sixth embodiment including any of the methods of the first through the fifth embodiments, wherein the fungicidal composition includes from about 25 g/L to about 300 g/L of the at least one N,N-dialkylcarboxamide, wherein the at least one N,N-dialkylcarboxamide includes an N,N-dimethyl fatty acid amide.

A seventh embodiment including any of the methods of the first through the sixth embodiments, wherein the fungicidal composition includes from about 25 g/L to about 150 g/L of the at least one of a ketone and an alcohol.

An eighth embodiment including any of the methods of the first through the seventh embodiments, wherein the fungicidal composition includes the at least one acetate ester, the at least one N,N-dialkylcarboxamide and the at least one of the ketone and the alcohol together form a water immiscible organic solvent.

A ninth embodiment including any of the methods of the first through the eighth embodiments, wherein the weight ratios of the at least one acetate ester:the at least one N,N-dialkylcarboxamide:the at least one of the ketone and the alcohol range from about 1-10:1-10:1-10.

A tenth embodiment including any of the methods of the first through the ninth embodiments, wherein the weight ratios of the at least one acetate ester:the N,N-dialkylcarboxamide:the at least one of the ketone and the alcohol range from about 4-6:1-3:1-2.

An eleventh embodiment including any of the methods of the first through the tenth embodiments wherein the at least one acetate ester is selected from a group consisting of benzyl acetate, cyclohexylmethyl acetate and phenyl acetate.

A twelfth embodiment including any of the methods of the first through the tenth embodiments wherein the at least one N,N-dialkylcarboxamide is selected from a group consisting of N,N-dimethylhexanamide, N,N-dimethyloctanamide, N,N-dimethyldecanamide and N,N-dimethyldodecanamide.

A thirteenth embodiment including any of the methods of the first through the twelfth embodiments, wherein the at least one of the ketone and the alcohol is selected from a group consisting of acetophenone, cyclohexanone, 2-ethylhexanol and 2-heptanol.

A fourteenth embodiment including any of the methods of the first through the thirteenth embodiments, wherein the water immiscible organic solvent includes benzyl acetate, one or more than one of a fatty acid N,N-dialkylcarboxamide and cyclohexanone.

A fifteenth embodiment including any of the methods of the first through the fourteenth embodiments, wherein fungicidal composition further comprising at least one additional fungicidal compound.

A sixteenth embodiment including any of the methods of the fifteenth embodiment, wherein the at least one additional fungicidal compound is selected from a group consisting of azoxystrobin, bifujunzhi, coumethoxystrobin, coumoxystrobin, dimoxystrobin, enestroburin, enoxastrobin, fenaminstrobin, fenoxystrobin, flufenoxystrobin, fluoxastrobin, jiaxiangjunzhi, kresoxim-methyl, mandestrobin, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyrametostrobin, pyraoxystrobin, triclopyricarb, trifloxystrobin, methyl 2-[2-(2,5-dimethylphenyloxymethyl)phenyl]-3-methoxyacrylate, azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, oxpoconazole, paclobutrazole, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, uniconazole, imazalil, pefurazoate, prochloraz, triflumizole, pyrimidines, fenarimol, nuarimol, pyrifenox, and triforine.

A seventh embodiment including any of the methods of the fifteenth or the sixteenth embodiments, wherein the at least one additional fungicidal compound is selected from a group consisting of azoxystrobin, kresoxim-methyl, picoxystrobin, pyraclostrobin, trifloxystrobin, epoxiconazole, fenbuconazole, myclobutanil, propiconazole, prothioconazole, and tebuconazole.

An eighteenth embodiment including any of the methods of the fifteenth through the seventeenths embodiments, wherein the at least one additional fungicidal compound is selected from a group consisting of pyraclostrobin, prothioconazole and propiconazole.

A nineteenth embodiment including any of the methods of the first through the eighteenth embodiments, wherein fungicidal composition further comprising an adjuvant that improves the fungicidal performance of the fungicidal composition selected from a group consisting of a non-ionic surfactant, a polyether modified organopolysiloxane and an alkyl phosphonate.

A twentieth embodiment including any of the methods of the first through the nineteenth embodiments, wherein the fungal plant pathogens include Septoria tritici, Puccinia triticina, Mycosphaerella graminicola, Puccinia triticina, Puccinia striiformis, Venturia inaequalis, Ustilago maydis, Uncinula necator, Rhynchosporium secalis, Leptosphaeria nodorum, Magnaporthe grisea, Monilinia fructicola, Pseudoperonospora cubensis, Pseudocercosporella herpotrichoides, Phakopsora pachyrhizi, Phaeosphaeria nodorum, Blumeria graminis tritici, Blumeria graminis hordei, Erysiphe cichoracearum, Ezysiphe graaminis, Glomerella lagenarium, Cercospora beticola, Alternaria solani, Rhizoctonia solani, Plasmopara viticola, Phytophthora infestans, Pyricularia oryzae, and Pyrenophora teres.

A twenty-first embodiment including any of the methods of the first through the twentieth embodiments, wherein the fungal plant diseases include anthracnose, blasts, botrytis, brown rust, blister smut, brown rot, downy mildew, fusarium, powdery mildew, rusts, glume blotch, leaf blotch, net blotch, sheath blight, stripe rust, scab, eye spot, leaf spot, early blight, and late blight.

A twenty-second embodiment including any of the methods of the first through the twenty-first embodiments, wherein the at least one ionic surfactant is an anionic surfactant selected from a group consisting of an alkali, alkaline earth and ammonium salt of an alkylarylsulfonic acid.

A twenty-third embodiment including any of the methods of the first through the twenty-second embodiments wherein the at least one nonionic surfactant is selected from a group consisting of an alcohol initiated EO/PO block copolymer and an alcohol ethoxylate.

DETAILED DESCRIPTION

Described herein is a fungicidal composition in the form of an emulsifiable concentrate (i.e., an emulsion concentrate or EC) that includes at least one a fungicidal compound, two or more surfactants and a water immiscible organic solvent comprised of a mixture of organic compounds including an acetate ester, an N,N-dialkylcarboxamide and at least one of a ketone and an alcohol. The described fungicidal composition exhibits good storage stability and readily forms a stable, homogenous emulsion upon dilution into a spray solution of water. The described fungicidal composition exhibits protectant and curative control of the important fungal diseases Septoria tritici (wheat leaf blotch) and Puccinia triticina (wheat brown rust) when utilized in spray applications.

Unless specifically or implicitly stated otherwise the term ‘about’ as used herein means plus or minus 10 percent. For example, ‘about 1.0’ encompasses the range of 0.9 to 1.1.

Provided herein is a fungicidal composition comprising:

    • a. a fungicidal compound of the Formula

    • b) at least one ionic surfactant; c) at least one nonionic surfactant; d) at least one acetate ester; e) at least one N,N-dialkylcarboxamide; and f) at least one of a ketone and an alcohol.

A. FIRST FUNGICIDAL COMPOUND

The fungicidal composition described herein is comprised of a first fungicidal compound of the Formula

which is a chemical derivative of the natural product UK-2A as described in U.S. Pat. No. 6,861,390 (the disclosure of which is hereby incorporated by reference in its entirety), and has the Chemical Abstracts (CAS) Number 517875-34-2 and the CAS name: propanoic acid, 2-methyl-, [[4-methoxy-2-[[[(3S,7R,8R,9S)-9-methyl-8-(2-methyl-1-oxopropoxy)-2,6-dioxo-7-(phenylmethyl)-1,5-dioxonan-3-yl]amino]carbonyl]-3-pyridinyl]oxy]methyl ester. The first fungicidal compound exhibits biological control of certain fungal diseases such as, for example, Septoria tritici (SEPTTR; wheat leaf blotch) and Puccinia triticina (PUCCRT; wheat brown rust). The first fungicidal compound will be referred to herein as Compound A.

In some embodiments the fungicidal compositions described herein may comprise, with respect to the composition, from about 1 gram of active ingredient per liter (g ai/L) to about 200 g ai/L, from about 5 g ai/L to about 175 g ai/L, from about 10 g ai/L to about 150 g ai/L, from about 20 g ai/L to about 125 g ai/L, from about 20 g ai/L to about 100 g ai/L, from about 20 g ai/L to about 90 g ai/L, from about 30 g ai/L to about 90 g ai/L, from about 40 g ai/L to about 90 g ai/L, from about 40 g ai/L to about 80 g ai/L, from about 45 g ai/L to about 75 g ai/L, or from about 50 g ai/L to about 70 g ai/L of Compound A. The fungicidal compositions described herein may also comprise, with respect to the composition, from about 30 g ai/L to about 150 g ai/L, from about 40 g ai/L to about 150 g ai/L, from about 50 g ai/L to about 150 g ai/L, from about 60 g ai/L to about 150 g ai/L, from about 70 g ai/L to about 150 g ai/L, from about 80 g ai/L to about 150 g ai/L, from about 90 g ai/L to about 150 g ai/L, from about 100 g ai/L to about 150 g ai/L, from about 125 g ai/L to about 150 g ai/L, from about 50 g ai/L to about 140 g ai/L, from about 50 g ai/L to about 130 g ai/L, from about 50 g ai/L to about 120 g ai/L, from about 50 g ai/L to about 110 g ai/L, from about 50 g ai/L to about 100 g ai/L, from about 50 g ai/L to about 90 g ai/L, or from about 50 g ai/L to about 80 g ai/L of Compound A.

B. SURFACTANTS

The fungicidal composition described herein may include more than one surfactant which may include one or more than one each of an ionic and a non-ionic surfactant. Such surfactants may be used as an emusifier, dispersant, solubilizer, wetter, penetrant, protective colloid, or for other purposes. Examples of surfactants are listed in McCutcheon's, Vol. 1: Emulsifiers & Detergents, McCutcheon's Directories, Glen Rock, USA, 2008 (International Ed. or North American Ed.). Since the described fungicidal composition is an emulsifiable concentrate (EC), surfactants are used to emulsify the EC when it is added to spray water so it forms a stable and homogeneous emulsion that can be readily applied by spray application to control target pests.

Suitable ionic surfactants for use with the fungicidal composition described herein may include anionic surfactants such as alkali, alkaline earth or ammonium salts of sulfonates, sulfates, phosphates, carboxylates, and mixtures thereof. Examples of sulfonates are alkylarylsulfonates, diphenylsulfonates, alpha-olefin sulfonates, lignin sulfonates, sulfonates of fatty acids and oils, sulfonates of ethoxylated alkylphenols, sulfonates of alkoxylated arylphenols, sulfonates of condensed naphthalenes, sulfonates of dodecyl- and tridecylbenzenes, sulfonates of naphthalenes and alkylnaphthalenes, sulfosuccinates or sulfosuccinamates. Examples of sulfates are sulfates of fatty acids and oils, of ethoxylated alkylphenols, of alcohols, of ethoxylated alcohols, or of fatty acid esters. Examples of phosphates are phosphate esters. Examples of carboxylates are alkyl carboxylates, and carboxylated alcohol or alkylphenol ethoxylates. Preferred anionic surfactants are sulfates and sulfonates.

In some embodiments the ionic surfactant for use with the fungicidal composition described herein may include an anionic surfactant such as an alkali, alkaline earth or ammonium salt of an alkylarylsulfonic acid such as sulfonate salts of dodecyl- and/or tridecylbenzenes, sulfonate salts of naphthalenes and/or alkylnaphthalenes, and salts of sulfosuccinates and/or sulfosuccinamates. In some embodiments the ionic surfactant is an alkaline earth salt of an alkylaryl sulfonate. In some embodiments the ionic surfactant is calcium dodecylbenzene sulfonate which is available as Nansa® EVM 70/2E from Huntsman International LLC (The Woodlands, Tex.).

In some embodiments the fungicidal composition described herein may comprise, with respect to the composition, from about 1 gram per liter (g/L) to about 100 g/L, from about 5 g/L to about 100 g/L, from about 10 g/L to about 100 g/L, from about 20 g/L to about 100 g/L, from about 30 g/L to about 100 g/L, from about 30 g/L to about 90 g/L, from about 30 g/L to about 80 g/L, from about 40 g/L to about 70 g/L, from about 50 g/L to about 70 g/L, or from about 55 g/L to about 65 g/L of at least one of an ionic surfactant.

In some embodiments, the fungicidal composition described herein may include a surfactant that is a nonionic surfactant. Suitable nonionic surfactants for use with the fungicidal compositions described herein may include alkoxylates, N-substituted fatty acid amides, amine oxides, esters, sugar-based surfactants, polymeric surfactants, and mixtures thereof. Examples of alkoxylates are compounds such as alcohols, alkylphenols, amines, amides, arylphenols, fatty acids or fatty acid esters which have been alkoxylated with from 1 to 50 molar equivalents of an alkoxylating agent such as ethylene oxide (EO) and/or propylene oxide (PO).

In some embodiments the fungicidal composition described herein may include a nonionic surfactant that is an alkoxylate such as, for example, an alcohol initiated EXPO block copolymer such as a butanol initiated EXPO block copolymer, which may also be known as a polyalkylene glycol monobutyl ether, a poly(ethylene glycol-co-propylene glycol) monobutyl ether, or a propylene oxide ethylene oxide polymer monobutyl ether. In some embodiments the butanol initiated EXPO block copolymer may have a degree of ethoxylation of from about 20 to about 30 and a degree of propoxylation of from about 20 to about 30. Suitable examples of these EXPO block copolymers may include Toximul® 8320 available from Stepan (Northfield, Ill.), Termul® 5429 available from Huntsman International LLC (The Woodlands, Tex.), Tergitol™ XD available from Dow Chemical (Midland, Mich.), and Ethylan™ NS 500 LQ available from AkzoNobel (Chicago, Ill.).

In some embodiments the fungicidal composition described herein may include a nonionic surfactant that is an alkoxylate such as, for example, an alcohol initiated EO/PO block copolymer like a 4-butoxy-1-butanol initiated EO/PO block copolymer (CAS number 99821-01-9) of which Atlas™ G5000 and Atlas™ G5002L are examples, and which are available from Croda (Edison, N.J.). In some embodiments the 4-butoxy-1-butanol initiated EO/PO block copolymer may have a degree of ethoxylation of from about 20 to about 30 and a degree of propoxylation of from about 20 to about 30.

In some embodiments the nonionic surfactant for use with the fungicidal composition described herein that is an alcohol initiated EO/PO block copolymer may provide improved active ingredient stability to the composition.

In some embodiments the fungicidal composition described herein may include a nonionic surfactant that is an alcohol ethoxylate such as a tridecyl alcohol ethoxylate, of which Synperonic™ 13/10, available from Croda (Edison, N.J.), is a suitable example which includes 10 EO units (degree of ethoxylation of 10).

In some embodiments the fungicidal composition described herein may include surfactants selected from the group consisting of at least one ionic surfactant that is an anionic surfactant and at least two non-ionic surfactants.

In some embodiments the fungicidal composition described herein may comprise, with respect to the composition, from about 1 gram per liter (g/L) to about 200 g/L, from about 10 g/L to about 190 g/L, from about 10 g/L to about 180 g/L, from about 20 g/L to about 160 g/L, from about 30 g/L to about 150 g/L, from about 40 g/L to about 140 g/L, from about 50 g/L to about 130 g/L, from about 60 g/L to about 120 g/L, from about 70 g/L to about 110 g/L, from about 80 g/L to about 100 g/L, or from about 85 g/L to about 95 g/L of at least one of a non-ionic surfactant.

C. WATER IMMISCIBLE ORGANIC SOLVENT

In certain embodiments, the described fungicidal composition includes a water immiscible organic solvent. “Water immiscible organic solvent” as defined herein means an organic solvent that has low water solubility and when mixed with an equivalent volume of water forms two discrete liquid layers. In some embodiments, the described fungicidal composition includes a water immiscible organic solvent that has a solubility in water of not greater than about 500 mg/L, about 600 mg/L, about 700 mg/L, about 800 mg/L, about 900 mg/L, or about 1000 mg/L. In some embodiments, the described composition includes a water immiscible organic solvent that has solubility in water of not greater than about 1250 mg/L, about 1500 mg/L, about 1750 mg/L, about 2000 mg/L, about 3000 mg/L, about 5000 mg/L, about 10,000 mg/L, about 20,000 mg/L, about 30,000 mg/L, about 40,000 mg/L, or about 50,000 mg/L.

In some embodiments, the water immiscible organic solvent serves as a liquid medium that dissolves the active and inert ingredients of the described fungicidal composition to form a stable solution (i.e., an emulsifiable concentrate) that forms a stable emulsion when added to water.

In some embodiments, the water immiscible organic solvent is comprised of a mixture of at least three organic compounds or classes of organic compounds. These organic compounds may be selected from the chemical classes of ester compounds, amide compounds, ketone compounds, and alcohol compounds. The organic compounds that make up the water immiscible organic solvent may be derived from natural sources such as vegetable, seed or animal oils, and/or from petrochemical sources.

In some embodiments, the fungicidal composition described herein includes a water immiscible organic solvent comprising of a mixture of organic compounds including at least one each of: an acetate ester, an N,N-dialkylcarboxamide, and at least one of a ketone and an alcohol.

In some embodiments, the fungicidal composition described herein includes a water immiscible organic solvent comprising of a mixture of organic compounds including at least one each of: an acetate ester and an N,N-dialkylcarboxamide.

Suitable organic compounds that may comprise the water immiscible organic solvent of the fungicidal composition described herein that are acetate esters may include compounds such as, for example, n-butyl acetate, iso-butyl acetate, n-pentyl acetate, iso-pentyl acetate, n-hexyl acetate, iso-hexyl acetate, cyclohexyl acetate, phenyl acetate, n-heptyl acetate, iso-heptyl acetate, cyclohexylmethyl acetate, benzyl acetate, or mixtures thereof. Benzyl acetate is available as Jeffsol AG-1705 from Huntsman (The Woodlands, Tex.).

In some embodiments, the described fungicidal composition may include, with respect to the composition, from about 50 g/L to about 700 g/L, from about 100 g/L to about 700 g/L, from about 150 g/L to about 700 g/L, from about 200 g/L to about 700 g/L, from about 250 g/L to about 700 g/L, from about 275 g/L to about 650 g/L, from about 300 g/L to about 600 g/L, from about 350 g/L to about 550 g/L, from about 375 g/L to about 550 g/L, from about 375 g/L to about 500 g/L, or from about 400 g/L to about 475 g/L of an acetate ester.

In some embodiments, suitable organic compounds that may comprise the water immiscible organic solvent of the described fungicidal composition may include benzyl acetate, cyclohexylmethyl acetate, phenyl acetate, or mixtures thereof.

In some embodiments, suitable organic compounds that may comprise the water immiscible organic solvent of the described fungicidal composition may include benzyl acetate.

Suitable organic compounds that may comprise the water immiscible organic solvent of the fungicidal composition described herein that are N,N-dialkylcarboxamides include the naturally derived fatty acid dimethylamides such as, e.g., N,N-dimethylcaprylamide (N,N-dimethyloctanamide), N,N-dimethylcapramide (N,N-dimethyldecanamide), and mixtures thereof, which may also be known as the N,N-dimethyl fatty acid amides and are available commercially as Agnique® AMD 810 and Agnique® AMD 10, from BASF Corp. (Florham Park, N.J.), Genegen® 4166, Genegen® 4231 and Genegen® 4296, from Clariant (Charlotte, N.C.), Hallcomid M-8-10 and Hallcomid M-10, from Stepan (Northfield, Ill.), and Armid DM10 and Armid DM810 from AkzoNobel (Chicago, Ill.). These products may also include small amounts of N,N-dimethylhexanamide and/or N,N-dimethyldodecanamide. Additional examples of naturally derived organic compounds that are N,N-dialkylcarboxamides include the morpholine amides of caprylic/capric fatty acids (C8/C10) which are commercially available as JEFFSOL® AG-1730 Solvent from Huntsman International LLC (The Woodlands, Tex.).

In some embodiments, the described fungicidal composition may include, with respect to the composition, from about 25 g/L to about 300 g/L, from about 25 g/L to about 300 g/L, from about 50 g/L to about 300 g/L, from about 75 g/L to about 300 g/L, from about 100 g/L to about 300 g/L, from about 125 g/L to about 300 g/L, from about 150 g/L to about 300 g/L, from about 175 g/L to about 300 g/L, from about 175 g/L to about 250 g/L, from about 175 g/L to about 200 g/L, from about 200 g/L to about 250 g/L, from about 225 g/L to about 300 g/L, from about 250 g/L to about 300 g/L, or from about 270 g/L to about 300 g/L of at least one N,N-dialkylcarboxamide.

In some embodiments, the described fungicidal composition may include one or more than one a N,N-dialkylcarboxamide selected from the group consisting of N,N-dimethylcaprylamide, N,N-dimethylcapramide, or mixtures thereof.

Suitable organic compounds that may comprise the water immiscible organic solvent of the fungicidal composition described herein that are at least one of a ketone and an alcohol may include compounds such as, acetophenone, cyclohexanone, ethyl isopropyl ketone, 2-heptanone, 2-hexanone, isophorone, methyl isobutyl ketone, 3-methyl-2-pentanone, 2-pentanone, 3-pentanone, trimethylcyclohexanone (dihydroisophorone), cyclohexanol, 2-heptanol, 2-ethylhexanol, and straight chain alcohols such as, for example, 1-hexanol, 1-heptanol, 1-octanol, 1-nonanol, 1-decanol, and the like, fatty alcohols such as oleyl alcohol and the like, and mixtures thereof.

In some embodiments, the described fungicidal composition may include, with respect to the composition, from about 25 g/L to about 150 g/L, from about 50 g/L to about 150 g/L, from about 50 g/L to about 125 g/L, from about 60 g/L to about 120 g/L, from about 70 g/L to about 120 g/L, from about 70 g/L to about 110 g/L, from about 70 g/L to about 100 g/L, or from about 70 g/L to about 90 g/L, of at least one of a ketone and an alcohol.

In some embodiments, the at least one of a ketone and an alcohol included in the described fungicidal composition may be selected from the group consisting of acetophenone, cyclohexanone, 2-ethylhexanol, 2-heptanol, and mixtures thereof.

In some embodiments, the at least one of a ketone and an alcohol included in the described fungicidal composition may be selected from the group consisting of acetophenone, cyclohexanone, and mixtures thereof.

In some embodiments, the at least one of a ketone and an alcohol included in the described fungicidal composition may be cyclohexanone.

In some embodiments, the at least one of a ketone and an alcohol included in the described fungicidal composition may provide improved solubility of Compound A in the described fungicidal composition.

In some embodiments, the at least one of a ketone and an alcohol included in the described fungicidal composition that is cyclohexanone, may provide improved solubility of Compound A in the described fungicidal composition.

In some embodiments, the water immiscible organic solvent may provide unexpected beneficial or synergistic effects to the described fungicidal composition such as, for example: (1) improved fungicidal performance of the composition when applied in spray applications to plants, (2) improved active ingredient solubility in the described compositions, and/or (3) improved Compound A chemical stability in the described composition during storage.

In some embodiments, the water immiscible organic solvent of the described fungicidal composition may provide unexpected beneficial or synergistic effects such as the formation of a stable, homogenous emulsifiable concentrate that readily emulsifies and forms a stable, oil-in-water emulsion without appreciable crystallization or precipitation of any of the ingredients when the composition is added to water.

In some embodiments, the water immiscible organic solvent of the fungicidal compositions described herein may include benzyl acetate, one or more than one of a fatty acid N,N-dimethylcarboxamide and cyclohexanone.

In some embodiments, the water immiscible organic solvent of the fungicidal compositions described herein may include benzyl acetate and one or more than one of a fatty acid N,N-dimethylcarboxamide.

The water immiscible organic solvent that may provide the unexpected beneficial or synergistic effects to the fungicidal composition described herein may depend on the selection of and/or the relative ratios of the organic compounds that comprise the water immiscible organic solvent.

In some embodiments, the ratio of the organic compounds included in the water immiscible organic solvent of the fungicidal composition described herein may range, on a weight basis, from about 1-10: 1-10:1-10 of the acetate ester:the one or more than one of the fatty acid N,N-dimethylcarboxamide:the at least one of a ketone and an alcohol. In some embodiments, the ratio of the organic compounds may range from about 1-8: 1-5:1-5, from about 1-6: 1-3:1-2, from about 2-6: 1-3:1-2, from about 3-6: 1-3:1-2, from about 4-6: 1-3:1-2, from about 4-5:1.5-2.5:0.5-1.5, or from about 4.5-5:1.8-2.2:0.8-1.2 of the acetate ester:the one or more than one of the fatty acid N,N-dimethylcarboxamide:the at least one of a ketone and an alcohol, on a weight basis.

In some embodiments, the ratio of the organic compounds included in the water immiscible organic solvent of the fungicidal composition described herein may range, on a weight basis, from about 4-6: 1-3:1-2, from about 4-5:1.5-2.5:0.7-1.2, or from about 4.5-5:1.9-2.3:0.8-1.1, of benzyl acetate:the one or more than one of a fatty acid N,N-dimethylcarboxamide:cyclohexanone.

In some embodiments, the ratio of the organic compounds included in the water immiscible organic solvent of the fungicidal composition described herein may range, on a weight basis, from about 1-10: 1-10 of the acetate ester:the one or more than one of the fatty acid N,N-dimethylcarboxamide. In some embodiments, the ratio of the organic compounds in the water immiscible organic solvent may range from about 1-5: 1-5, from about 1-5: 1-2, from about 1-4: 1-2, from about 1-3: 1-2, from about 1-3:1, from about 4:1, from about 3:1, from about 2:1, or from about 1:1 of benzyl acetate:the one or more than one of a fatty acid N,N-dimethylcarboxamide.

In some embodiments, the described fungicidal composition exhibits beneficial or synergistic properties related to the composition of the water immiscible organic solvent such as improved fungicidal efficacy after spray application of the composition to vegetation or an area adjacent thereto to prevent the growth of fungal pathogens or diseases.

In some embodiments, the described fungicidal composition exhibits beneficial or synergistic properties related to the composition of the water immiscible organic solvent such as improved fungicidal control of Septoria tritici (SEPTTR; wheat leaf blotch) and Puccinia triticina (PUCCRT; wheat brown rust) after spray application of the composition to vegetation or an area adjacent thereto to prevent the growth of the fungal pathogens or diseases.

In some embodiments, the described fungicidal composition exhibits beneficial or synergistic properties related to the composition of the water immiscible organic solvent such as improved active ingredient chemical stability during storage.

In some embodiments, the described fungicidal composition exhibits beneficial or synergistic properties related to the composition of the water immiscible organic solvent such as improved active ingredient solubility in the composition.

D. ADDITIONAL FUNGICIDAL COMPOUND

In certain embodiments, the described fungicidal composition may include at least one additional fungicidal compound. Suitable at least one additional fungicidal compounds may include, for example, azoxystrobin, bifujunzhi, coumethoxystrobin, coumoxystrobin, dimoxystrobin, enestroburin, enoxastrobin, fenaminstrobin, fenoxystrobin, flufenoxystrobin, fluoxastrobin, jiaxiangjunzhi, kresoxim-methyl, mandestrobin, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyrametostrobin, pyraoxystrobin, triclopyricarb, trifloxystrobin, methyl 2-[2-(2,5-dimethylphenyloxymethyl)phenyl]-3-methoxyacrylate, pyribencarb, triclopyricarb/chlorodincarb, famoxadon, fenamidon, cyazofamid, amisulbrom, benodanil, bixafen, boscalid, carboxin, fenfuram, fluopyram, flutolanil, fluxapyroxad, furametpyr, isopyrazam, mepronil, oxycarboxin, penflufen, penthiopyrad, sedaxane, tecloftalam, thifluzamide, N-(4′-trifluoromethylthio-biphenyl-2-yl)-3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxamide, N-(2-(1,3,3-trimethylbutyl)phenyl)-1,3-dimethyl-5-fluoro-1H-pyrazole-4-carboxamide, N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, diflumetorim, binapacryl, dinobuton, dinocap, meptyl-dinocap, fluazinam, ferimzone, ametoctradin, silthiofam, azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, oxpoconazole, paclobutrazole, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, uniconazole, imazalil, pefurazoate, prochloraz, triflumizole, pyrimidines, fenarimol, nuarimol, pyrifenox, triforine, aldimorph, dodemorph, dodemorph acetate, fenpropimorph, tridemorph, fenpropidin, piperalin, spiroxamine, fenhexamid, benalaxyl, benalaxyl-M, kiralaxyl, metalaxyl, metalaxyl-M (mefenoxam), ofurace, oxadixyl, hymexazole, octhilinone, oxolinic acid, bupirimate, benomyl, carbendazim, fuberidazole, thiabendazole, thiophanate-methyl, 5-chloro-7-(4-methyl-piperidin-1-yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine, diethofencarb, ethaboxam, pencycuron, fluopicolid, zoxamid, metrafenon, pyriofenon, cyprodinil, mepanipyrim, pyrimethanil, fluoroimide, iprodione, procymidone, vinclozolin, fenpiclonil, fludioxonil, quinoxyfen, edifenphos, iprobenfos, pyrazophos, isoprothiolane, dicloran, quintozene, tecnazene, tolclofos-methyl, biphenyl, chloroneb, etridiazole, dimethomorph, flumorph, mandipropamid, pyrimorph, benthiavalicarb, iprovalicarb, valifenalate and 4-fluorophenyl N-(1-(1-(4-cyanophenyl)ethanesulfonyl)but-2-yl)carbamate, propamocarb, propamocarb hydrochloride, ferbam, mancozeb, maneb, metiram, propineb, thiram, zineb, ziram, anilazine, chlorothalonil, captafol, captan, folpet, dichlofluanid, dichlorophen, flusulfamide, hexachlorobenzene, pentachlorophenol, phthalid, tolylfluanid, N-(4-chloro-2-nitrophenyl)-N-ethyl-4-methylbenzenesulfonamide, guanidine, dithianon, validamycin, polyoxin B, pyroquilon, tricyclazole, carpropamid, dicyclomet, fenoxanil, and mixtures thereof.

In some embodiments, the described composition may include at least one additional fungicidal compound selected from azoxystrobin, bifujunzhi, coumethoxystrobin, coumoxystrobin, dimoxystrobin, enestroburin, enoxastrobin, fenaminstrobin, fenoxystrobin, flufenoxystrobin, fluoxastrobin, jiaxiangjunzhi, kresoxim-methyl, mandestrobin, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyrametostrobin, pyraoxystrobin, triclopyricarb, trifloxystrobin, methyl 2-[2-(2,5-dimethylphenyloxymethyl)phenyl]-3-methoxyacrylate, azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, oxpoconazole, paclobutrazole, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, uniconazole, imazalil, pefurazoate, prochloraz, triflumizole, pyrimidines, fenarimol, nuarimol, pyrifenox, triforine, and mixtures thereof.

In some embodiments, the described composition may include at least one additional fungicidal compound selected from benodanil, bixafen, boscalid, carboxin, fenfuram, fluopyram, flutolanil, fluxapyroxad, furametpyr, isopyrazam, mepronil, oxycarboxin, penflufen, penthiopyrad, sedaxane, thifluzamide, and mixtures thereof.

In some embodiments, the described composition may include at least one additional fungicidal compound selected from azoxystrobin, kresoxim-methyl, picoxystrobin, pyraclostrobin, trifloxystrobin, epoxiconazole, fenbuconazole, myclobutanil, propiconazole, prothioconazole, tebuconazole, and mixtures thereof.

In some embodiments, the described fungicidal composition may include the fungicidal compound pyraclostrobin.

In some embodiments, the described fungicidal composition may include the fungicidal compound prothioconazole.

In some embodiments, the described fungicidal composition may include the fungicidal compound propiconazole.

In some embodiments, the described fungicidal composition that includes at least one additional fungicidal compound may show synergistic fungicidal activity.

In some embodiments the fungicidal composition described herein may comprise, with respect to the composition, from about 1 gram active ingredient per liter (g ai/L) to about 200 g ai/L, from about 5 g ai/L to about 175 g ai/L, from about 10 g ai/L to about 150 g ai/L, from about 20 g ai/L to about 150 g ai/L, from about 20 g ai/L to about 125 g ai/L, from about 20 g ai/L to about 100 g ai/L, from about 20 g ai/L to about 90 g ai/L, from about 30 g ai/L to about 90 g ai/L, from about 40 g ai/L to about 90 g ai/L, from about 40 g ai/L to about 80 g ai/L, from about 45 g ai/L to about 75 g ai/L, or from about 45 g ai/L to about 70 g ai/L of the at least one additional fungicidal compound. The fungicidal composition described herein may also comprise from about from about 30 g ai/L to about 150 g ai/L, from about 40 g ai/L to about 150 g ai/L, from about 50 g ai/L to about 150 g ai/L, from about 60 g ai/L to about 150 g ai/L, from about 70 g ai/L to about 150 g ai/L, from about 80 g ai/L to about 150 g ai/L, from about 90 g ai/L to about 150 g ai/L, from about 100 g ai/L to about 150 g ai/L, from about 110 g ai/L to about 150 g ai/L, from about 120 g ai/L to about 150 g ai/L, from about 125 g ai/L to about 140 g ai/L, or from about 125 g ai/L to about 135 g ai/L of the at least one additional fungicidal compound.

E. ADJUVANTS

Adjuvants are compounds which have negligible or even no pesticidal activity themselves, and which improve the biological performance of a pesticidal composition on one or more target pests. Examples of such adjuvants may include surfactants such as alcohol ethoxylates, alkyl naphthalene sulphonates, alkyl phosphonates, alkylbenzene sulphonates, benzyldimethylcocalkyl ammonium salts, sorbitan ester ethoxylates, and modified organosilicones; also, mineral or vegetable oils, and other auxilaries. Further examples of adjuvants are listed by Knowles in, “Adjuvants and Additives,” Agrow Reports DS256, T&F Informa UK, 2006, Chapter 5.

In some embodiments, the fungicidal composition described herein may include an adjuvant to improve fungicidal performance.

In some embodiments, the fungicidal composition described herein may include an adjuvant to improve fungicidal performance selected from the class of modified organosilicone surfactants such as, for example, the polyether modified organopolysiloxanes such as Break-thru® S233, which is available from Evonik Industries (Parsippany, N.J.).

In some embodiments, the fungicidal composition described herein may include an adjuvant to improve fungicidal performance selected from the class of alkyl phosphonate adjuvants such as, for example, bis(2-ethylhexyl) 2-ethylhexylphosphonate (also known as BEEP), which is available from Rhodia (Cranberry, N.J.).

In some embodiments, non-ionic surfactants such as, for example, a tridecyl alcohol ethoxylate (i.e., Synperonic 13/10) may serve as an adjuvant that improves the fungicidal performance of the fungicidal composition described herein.

In some embodiments, the fungicidal composition described herein may include, with respect to the composition, from about 1 g/L to about 200 g/L of one or more adjuvants used to improve fungicidal performance. In some embodiments, the fungicidal composition may include from about 1 g/L to about 150 g/L, from about 5 g/L to about 150 g/L, from about 10 g/L to about 150 g/L, from about 20 g/L to about 150 g/L, from about 25 g/L to about 140 g/L, from about 30 g/L to about 130 g/L, from about 35 g/L to about 125 g/L, from about 40 g/L to about 120 g/L, from about 40 g/L to about 110 g/L, from about 40 g/L to about 100 g/L, from about 40 g/L to about 90 g/L, from about 40 g/L to about 80 g/L, from about 40 g/L to about 70 g/L, from about 50 g/L to about 70 g/L, from about 40 g/L to about 130 g/L, from about 50 g/L to about 120 g/L, from about 60 g/L to about 120 g/L, from about 70 g/L to about 120 g/L, from about 80 g/L to about 120 g/L, from about 90 g/L to about 120 g/L, or from about 100 g/L to about 120 g/L, of one or more adjuvants used to improve fungicidal performance.

F. STORAGE STABILITY

As used herein, stable compositions are compositions that are stable physically and/or chemically for defined periods of time to the environments in which they are produced, transported and/or stored. Aspects of stable compositions include, but are not limited to: physical stability at temperatures that range from about 0° C. to about 54° C., homogeneity, pourability, liquids that form little or no precipitated solids or crystals or exhibit little or no phase separation, compositions that readily emulsify when poured into a spray tank of water and retain their biological efficacy when applied, for example, by spray application to target pests.

In some embodiments, the described composition forms a stable, homogeneous emulsifiable concentrate that does not exhibit appreciable phase separation under the storage conditions. In some embodiments, the described composition exhibits very little change in viscosity under the storage conditions. In some embodiments, the described composition exhibits very little chemical decomposition of the active ingredient or active ingredients under the storage conditions.

In some embodiments, the described fungicidal composition is stable at temperatures of greater than or equal to about 25° C. for a period of at least 2, 4, 6 or 8 weeks. In some embodiments, the described composition is stable at temperatures of greater than or equal to about 40° C. for a period of at least 2, 4, 6 or 8 weeks. In some embodiments, the described composition is stable at temperatures of greater than or equal to about 54° C. for a period of at least about 2 weeks.

In some embodiments, the described fungicidal composition does not exhibit or does not significantly exhibit separation, precipitation or crystallization of any of the components at low temperatures. In some embodiments, the described fungicidal composition remains as a homogeneous emulsifiable concentrate after storage for at least about 2 weeks at temperatures below about 20° C., below about 10° C., or equal to or less than about 5° C., or equal to or less than about 0° C., or equal to or less than about −5° C., or equal to or less than about −10° C. In certain embodiments, the compositions are stable at these temperatures for at least about 2, 4, 6, or 8 weeks.

In some embodiments, the described fungicidal composition remains as a homogeneous concentrate after subjecting it to freeze/thaw (F/T) conditions for at least about 2 or 4 weeks where the temperature is cycled from about −10° C. to about 40° C. every 24 hours.

In some embodiments, the storage stability of the described fungicidal composition may be dependent on one or more ingredients and their concentration in the composition. Such ingredients may include, but are not limited to, the organic compounds that comprise the water immiscible organic solvent, the nonionic surfactant, the at least one additional fungicidal compound, dialkylamines such as dimethylamine that are present in or formed from the N,N-dialkylcarboxamides, and water.

In some embodiments, the chemical stability of the active ingredient or active ingredients in the described fungicidal composition may be improved by including a ketone or an alcohol in the composition.

In some embodiments, the chemical stability of the active ingredient or active ingredients in the described fungicidal composition may be improved by including a nonionic surfactant in the composition.

In some embodiments, the chemical stability of the active ingredient or active ingredients in the described fungicidal composition may be improved by eliminating or reducing the amount of a dialkylamine in the composition.

In some embodiments, the chemical stability of the active ingredient or active ingredients in the described fungicidal composition may be improved by eliminating or reducing the amount of water in the composition.

In some embodiments, the chemical stability of the first active ingredient in the described fungicidal composition may be reduced by adding at least one additional fungicidal compound to the composition.

G. METHODS OF PREPARATION AND USE

Also described herein is a process or method for the preparation of the described fungicidal composition which includes mixing together the one or more fungicide active ingredients, the inert ingredients and the water immiscible organic solvent to form a stable, homogenous, emulsifiable concentrate that readily emulsifies to form a stable, homogeneous, emulsion when added to water.

In some embodiments, the fungicidal composition (emulsifiable concentrate) described herein may be prepared by the steps of:

(1) preparing a solution of the first fungicidal compound in the water immiscible organic solvent;

(2) adding one or more surfactants to the solution prepared in step (1) to form a solution;

(3) optionally, adding at least one additional fungicidal compound to the solution prepared in step (2); and

(4) optionally, adding any additional compatible active or inert ingredients to the solution prepared in step (3) to from a solution.

The described fungicidal composition may also be prepared by changing the relative order of the steps, or adding or eliminating steps to the preparation described herein as may be readily determined by one of ordinary skill in the art.

The disclosure furthermore relates to an emulsion obtainable (preferably obtained) by mixing water with the emulsifiable concentrate described herein. The emulsion normally arises spontaneously upon mixing. In most cases, the emulsion is an oil-in-water emulsion. The mixing ratio of water to concentrate may be in the range of from 1000 to 1 up to 1 to 1, preferably 200 to 1 up to 3 to 1.

Also provided herein is a method of controlling plant derived fungal pathogens or diseases comprising contacting the vegetation or an area adjacent thereto to prevent the growth of the fungal pathogens or diseases a fungicidally effective amount of a fungicidal composition comprising:

    • a) a fungicidal compound of the Formula

    • b) at least one ionic surfactant;
    • c) at least one nonionic surfactant;
    • d) an acetate ester;
    • e) an N,N-dialkylcarboxamide; and
    • f) at least one of a ketone and an alcohol.

Plant fungal pathogens that may be controlled by the described fungicidal compositions include Septoria tritici, Puccinia triticina, Mycosphaerella graminicola, Puccinia triticina, Puccinia striiformis, Venturia inaequalis, Ustilago maydis, Uncinula necator, Rhynchosporium secalis, Leptosphaeria nodorum, Magnaporthe grisea, Monilinia fructicola, Pseudoperonospora cubensis, Pseudocercosporella herpotrichoides, Phakopsora pachyrhizi, Phaeosphaeria nodorum, Blumeria graminis tritici, Blumeria graminis hordei, Erysiphe cichoracearum, Ezysiphe graaminis, Glomerella lagenarium, Cercospora beticola, Alternaria solani, Rhizoctonia solani, Plasmopara viticola, Phytophthora infestans, Pyricularia oryzae, and Pyrenophora teres.

Plant fungal diseases that may be controlled by the described fungicidal compositions include anthracnose, blasts, botrytis, brown rust, blister smut, brown rot, downy mildew, fusarium, powdery mildew, rusts, glume blotch, leaf blotch, net blotch, sheath blight, stripe rust, scab, eye spot, leaf spot, early blight, and late blight.

In some embodiments, the described fungicidal composition, after spray application to plant surfaces, exhibits rainfast properties by offering good fungicidal efficacy after exposure to rain or other moisture causing events.

This described method includes use of the described fungicidal composition for protecting a plant against attack by a phytopathogenic organism or the treatment of a plant already infested by a phytopathogenic organism, comprising the step of applying the described fungicidal composition, to soil, a plant, a part of a plant, foliage, flowers, fruit, and/or seeds, or any surface adjacent to a plant in a disease inhibiting and phytologically acceptable amount. The term “disease inhibiting and phytologically acceptable amount” refers to an amount of a compound that kills or inhibits the plant disease for which control is desired, in an amount not significantly toxic to the plant being treated. The exact concentration of active compound required varies with the fungal disease to be controlled, the type of formulations employed, the method of application, the particular plant species, climate conditions, and the like, as is well known in the art.

The fungicidal compositions described herein may optionally be diluted in an aqueous spray mixture for agricultural application such as for the control of phytopathogenic fungi in crop fields. Such compositions are typically diluted with an inert carrier, such as water, before application. The diluted compositions, which are usually applied, for example, to crops, the locus of crops or the locus of where phytopathogenic fungi may eventually emerge, in some embodiments include about 0.0001 to about 1 weight percent of the active ingredient or from 0.001 to about 1 weight percent of the active ingredient. The present compositions can be applied, for example, to crop plants or their locus by the use of conventional ground or aerial sprayers, and by other conventional means known to those skilled in the art.

H. OPTIONAL INGREDIENTS

The compositions disclosed herein may optionally include inert formulation ingredients such as, but not limited to, dispersants, surfactants and wetting agents. These optional inert ingredients may include surfactants conventionally used in the art of formulation that are described, inter alia, in “McCutcheon's Detergents and Emulsifiers Annual,” MC Publishing Corp., Ridgewood, N.J., 1998 and in the “Encyclopedia of Surfactants,” Vol. I-III, Chemical Publishing Co., New York, 1980-81. These surface-active agents can be anionic, cationic or nonionic in character and can be employed as emulsifying agents, wetting agents, suspending agents, or for other purposes.

In addition to the specific methods and compositions set forth above, the methods and compositions described herein also may include compositions comprising one or more additional compatible ingredients. These additional ingredients may include, for example, one or more pesticides or other ingredients, which may be dissolved or dispersed in the composition and may be selected from acaricides, algicides, antifeedants, avicides, bactericides, bird repellents, chemosterilants, defoliants, desiccants, disinfectants, fungicides, herbicide safeners, herbicides, insect attractants, insecticides, insect repellents, mammal repellents, mating disrupters, molluscicides, nematicides, plant activators, plant growth regulators, rodenticides, semiochemicals, synergists, and virucides. Also, any other additional ingredients providing functional utility such as, for example, antifoam agents, antimicrobial agents, buffers, corrosion inhibitors, dispersing agents, dyes, fragrants, freezing point depressants, neutralizing agents, odorants, penetration aids, sequestering agents, spray drift control agents, spreading agents, stabilizers, sticking agents, viscosity-modifying additives, water soluble solvents and the like, may be included in these compositions.

When the described compositions are used in combination with the additional active ingredients such as, for example, insecticide active ingredients, the compositions described herein can be formulated with the other active ingredient or active ingredients as premix concentrates, tank-mixed in water with the other active ingredient or active ingredients for spray application, or applied sequentially with the other active ingredient or active ingredients in separate spray applications.

The compositions and methods described herein may be used in controlling fungal diseases in crops possessing single, multiple or stacked genomic traits conferring tolerance to one or more herbicide chemistries and/or inhibitors with single or multiple modes of action.

I. EXAMPLES

The following Examples are presented to illustrate various aspects of the compositions described herein and should not be construed as limitations to the claims.

Example 1 Preparation of Representative Samples of the Described Fungicidal Composition

TABLE 1 Fungicidal Compositions Described Herein Ingredient Role Amount (g/L) 1st fungicide cmpd. active ingredient 1-250 2nd fungicide cmpd. active ingredient 0-200 surfactant emulsifier 1-100 surfactant emulsifier 1-100 surfactant emulsifier 1-100 organosilicone adjuvant 10-100  ketone solvent 0-500 acetate ester solvent 10-750  N,N-dialkylcarboxamide1 solvent 10-500  polydimethylsiloxane antifoam 0.01-1    1Also known as an N,N-dimethyl fatty acid amide.

Sample 1:

An emulsion concentrate comprising Compound A as the active ingredient was prepared using the ingredients in Table 2 and as described in the steps below (indicated values are g per 100 mL formulation):

TABLE 2 Sample 1 Fungicidal Composition 1st fungicide cmpd Compound A, 85% tech. 5.88 surfactant Nansa EVM 70/2E 6.00 surfactant Toximul 8320 4.50 surfactant Synperonic 13/10 4.50 organosilicone Breakthru S233 5.00 ketone cyclohexanone 9.89 acetate ester benzyl acetate 46.81 N,N-dialkylcarboxamide Hallcomid M-8-10 19.03 polydimethylsiloxane SAG 1572 0.01

(1) An active ingredient premix of cyclohexanone, benzyl acetate, Hallcomid M-8-10 and Compound A was prepared. (2) The premix from (1) was warmed to 35-40° C. and stirred until a clear solution was obtained. (3) The remaining ingredients were added to the premix followed by mixing until a uniform composition was obtained.

Sample 2:

An emulsion concentrate comprising Compound A and prothioconazole active ingredients was prepared using the ingredients in Table 3 and as described in the steps below (indicated values are g per 100 mL formulation):

TABLE 3 Sample 2 Fungicidal Composition 1st fungicide cmpd Compound A, 85% technical 5.88 2nd fungicide cmpd prothioconazole 96% tech. 10.42 surfactant Nansa EVM 70/2E 6.00 surfactant Toximul 8320 4.50 surfactant Synperonic 13/10 4.50 organosilicone Breakthru S233 5.00 ketone Cyclohexanone 8.90 acetate ester Benzyl acetate 42.11 N,N-dialkylcarboxamide Hallcomid M-8-10 17.11 polydimethylsiloxane SAG 1572 0.01

(1) An active ingredient premix of cyclohexanone, benzyl acetate, Hallcomid M-8-10, prothioconazole and Compound A was prepared. (2) The premix from (1) was stirred until a clear solution was obtained. (3) The remaining ingredients were added to the premix followed by mixing until a uniform composition was obtained.

Sample 3:

An emulsion concentrate comprising Compound A and pyraclostrobin active ingredients was prepared using the ingredients in Table 4 and as described in the steps below (indicated values are g per 100 mL formulation):

TABLE 4 Sample 3 Fungicidal Composition 1st fungicide cmpd Compound A, 85% technical 5.88 2nd fungicide cmpd pyraclostrobin 98% tech. 6.38 surfactant Nansa EVM 70/2E 6.00 surfactant Toximul 8320 4.50 surfactant Synperonic 13/10 4.50 organosilicone Breakthru S233 5.00 ketone Cyclohexanone 9.29 acetate ester Benzyl acetate 43.82 N,N-dialkylcarboxamide Hallcomid M-8-10 17.86 polydimethylsiloxane SAG 1572 0.01

(1) A solvent premix of cyclohexanone, benzyl acetate and Hallcomid M-8-10 was prepared. (2) The premix from (1) was stirred until a clear solution was obtained. (3) The surfactants, adjuvant and antifoaming agent are added to the premix followed by mixing until a uniform composition was obtained. (4) The pyraclostrobin technical active ingredient was heated until molten (70° C.) and then added to the premix prepared in step (3) whilst mixing. (5) The Compound A technical active ingredient was added to the premix followed by mixing until a uniform composition was obtained.

Sample 4:

An emulsion concentrate comprising Compound A and prothioconazole active ingredients was prepared using the ingredients in Table 5 and as described in the steps below (indicated values are g per 100 mL formulation):

TABLE 5 Sample 4 Fungicidal Composition 1st fungicide cmpd Compound A, 85% tech. 7.85 2nd fungicide cmpd prothioconazole, 98% tech. 13.89 surfactant Nansa EVM 70/2E 6.00 surfactant Toximul 8320 4.50 surfactant Synperonic 13/10 4.50 organosilicone Breakthru S233 5.00 ketone Cyclohexanone 6.67 acetate ester Benzyl acetate 38.71 N,N-dialkylcarboxamide Hallcomid M-8-10 15.72 polydimethylsiloxane SAG 1572 0.01

(1) A solvent premix of cyclohexanone, benzyl acetate and Hallcomid M-8-10 was prepared. (2) The premix from (1) was stirred until a clear solution was obtained. (3) The surfactants, adjuvant and antifoaming agent were added to the premix followed by mixing until a uniform composition was obtained. (4) The prothioconazole and Compound A technical active ingredients were added to the premix followed by mixing until a uniform composition was obtained.

Sample 5:

An emulsion concentrate comprising Compound A and pyraclostrobin active ingredients was prepared using the ingredients and amounts listed in Table 6 in a manner similar to that described for Sample 3 (indicated values are g per 1 L formulation):

TABLE 6 Sample 5 Fungicidal Composition 1st fungicide cmpd Compound A, 85% tech. 66.7 g/L 2nd fungicide cmpd pyraclostrobin 98% tech. 83.3 surfactant Nansa EVM 70/2E 60 surfactant Toximul 8320 45 surfactant Synperonic 13/10 45 organosilicone Breakthru S233 66.7 ketone Cyclohexanone 86.9 acetate ester Benzyl acetate 410.2 N,N-dialkylcarboxamide Hallcomid M-8-10 181.2 polydimethylsiloxane SAG 1572 0.1

Sample 6:

An emulsion concentrate comprising Compound A and prothioconazole active ingredients was prepared using the ingredients and amounts listed in Table 7 in a manner similar to that described for Sample 3 (indicated values are in grams per 100 mL formulation):

TABLE 7 Sample 6 Fungicidal Composition 1st fungicide cmpd Compound A, 84% technical 5.95 2nd fungicide cmpd prothioconazole 96% tech. 7.81 surfactant Nansa EVM 70/2E 7.50 surfactant Toximul 8320 3.00 surfactant Synperonic 13/10 4.50 acetate ester Benzyl acetate 48.1 N,N-dialkylcarboxamide Hallcomid M-8-10 25.9

Sample 7:

An emulsion concentrate comprising Compound A and prothioconazole active ingredients was prepared using the ingredients and amounts listed in Table 8 in a manner similar to that described for Sample 3 (indicated values are in grams):

TABLE 8 Sample 7 Fungicidal Composition 1st fungicide cmpd Compound A, 84% technical 1.15 2nd fungicide cmpd prothioconazole 96% tech. 1.51 surfactant Nansa EVM 70/2E 1.49 surfactant Toximul 8320 0.60 surfactant Synperonic 13/10 0.89 organosilicone Breakthru S233 2.42 acetate ester Benzyl acetate 8.95 N,N-dialkylcarboxamide Hallcomid M-8-10 2.98

Sample 8:

An active ingredient premix of cyclohexanone, benzyl acetate, Hallcomid M-8-10, propiconazole and Compound A was prepared using the amounts shown in Table 9. The premix was stirred until a clear solution was obtained. The remaining ingredients were added to the premix followed by mixing until a uniform composition was obtained (indicated values are in g per 100 mL formulation):

TABLE 9 Sample 8 Fungicidal Composition Fungicide compound 1 Compound A, 85% technical 5.88 Fungicide compound 2 Propiconazole 92% technical 9.05 Surfactant Nansa EVM 70/2E 6.00 Surfactant Atlas G5002L 4.50 Surfactant Synperonic 13/10 4.50 Organosilicone Breakthru S233 5.00 Ketone Cyclohexanone 9.2 Acetate ester Benzyl acetate 43.10 N,N-dialkylcarboxamide Hallcomid M-8-10 16.76 polydimethylsiloxane SAG 1572 0.01

Example 2 Solubility of Fungicidal Active Ingredients in Organic Solvents

    • a) Relative solubility of Compound A and prothioconazole in organic solvents with low solubility in water.

To prepare an effective EC composition comprising Compound A and prothioconazole the following solvent attributes must be achieved:

    • Compound A solubility needs to be above 10 wt %
    • prothioconazole solubility needs to be above 20 wt %
    • water solubility of solvent candidates should be below about 5 g/L or 0.5% so that good emulsion stability will be achieved when the EC is added to water.

Test Method:

The approximate solubility of Compound A was determined by mixing a known mass of the active ingredient with an increasing mass of each solvent at ambient temperature. For example, 0.2 g of Compound A was mixed with 1.38 g of cyclohexanone giving a clear solution comprising 12.6% w/w Compound A. Cyclohexanone was therefore classified as a very good solvent for Compound A as it offered “High” solubility (see following table) and was included for further evaluation. The solubility of Compound A in the solvents used in this screening procedure was generally classified within the following concentration ranges:

Compound A Solubility (wt %) Relative Solubility >8.4 High 8.4 to 5.6 Medium 5.6 to 3.0 Low <3.0 Very Low

Prothioconazole Solubility (wt %) Relative Solubility >30 High >20 to 30 Medium  10 to 20 Low <10 Very Low

Table 9.1 shows the relative solubility of Compound A and prothioconazole in a variety of organic solvents.

TABLE 9.1 Relative Solubility of Compound A and Prothioconazole in Organic Solvents at Ambient Temperature Relative Relative Solubility Solubility Solubility of of Com- of Prothio- Solvent in Solvent pound A conazole Water (g/L)1 Cyclohexanone High High 8.6-25  Methyl-5-(Dimethylamino)-2- High High 79 Methyl-5-Oxopentanoate Benzyl alcohol High Medium 43 N-formyl morpholine and High Medium Miscible2 propylene carbonate Benzyl acetate High Low 1.0-3.1 Sulfolane High Low 379 Methyl salicylate High Very Low <5 Butyl benzoate Medium Low 1.7e−4 2-heptanone Medium Low 4.28 Pentanedioic acid, 2-methyl-1, Medium Low 25 5-dimethyl ester Butyl lactate Medium Low 42 Isopropyl benzoate Medium Very Low 0.64 N,N dimethyl fatty acid amides Low High 1.9-5.3 Tributoxyethyl phosphate Low High Miscible Diethylene glycol monoethyl Low High Miscible ether dimethyl esters of adipic, Low Low 53 glutaric and succinic acids Ethyl Diglycol Acetate Low Very Low Miscible 2-ethylhexyl lactate3 Very Low Medium 1.9 Polyethylene glycol Very Low Medium Miscible Polypropylene glycol Very Low Low Miscible 2-ethylhexanol Very Low Very Low 0.88 Methyl oleate Very Low Very Low 0.0011 Isoparaffin Very Low Very Low <5 Alkyl naphthalene mixture Very Low Very Low <5 Butylene carbonate Very Low Very Low 7 Soybean oil Very Low Very Low <5 Propylene carbonate Very Low Very Low 17.5 2-ethylhexyl benzoate Very Low Very Low 0.0004 Di-n-butyl carbonate Very Low Very Low 0.82 1Estimated from a survey of the literature; 2miscible means totally soluble in water in all amounts; 32-ethylhexyl lactate/Compound A mixture freezes at 0° C.
    • b) Solubility of Compound A and prothioconazole in benzyl acetate/AMD810 blends at 10° C.

A study of the Compound A and prothioconazole solubility in blends of benzyl acetate/AMD810 was conducted. To each solvent blend both actives were added until each was saturated and the resulting mixtures were then stored at 10° C. until equilibrium was obtained. Aliquots of the supernatant layer were taken from each sample, filtered (0.45 μm mesh) and analyzed by HPLC to determine the solution concentration of each active in the blends. Table 10 shows the results.

TABLE 10 Solubility of a Mixture of Compound A and Prothioconazole in Benzyl Acetate-AMD810 Blends at 10° C. Proportion of Benzyl Prothioconazole Compound A acetate to AMD810 in Solubility Solubility Blend (wt %) at 10° C. (% w/w) at 10° C. (% w/w) 0 31.3 3.3 20 32.3 4.3 40 33.1 6.5 60 32.1 11.0 80 26.6 12.0 100 16.2 14.3
    • c) Solubility of Compound A and prothioconazole in benzyl acetate/AMD810/cyclohexanone blends at 10° C.

The weight fraction of each solvent was tested at a variety of levels (from 0 to 1) in the various blends shown in Table 11. A total of 20 g of each solvent blend was prepared per sample. For example, one of the blends (Blend 4) was prepared by combining cyclohexanone 0.2 (4 g), benzyl acetate 0.2 (4 g) and AMD810 0.6 (12 g). To Blend 4 were added amounts of Compound A and prothioconazole technical active ingredients to achieve saturation concentrations of each. The samples were then stored at 10° C. for one week and then were analysed for soluble active ingredient content. The results are shown in Table 11.

TABLE 11 Solubility of Compound A and Prothioconazole in Benzyl Acetate/AMD810/Cyclohexanone Blends at 10° C. Com- Prothio- Solvent Ratio (weight fraction) pound A conazole Blend Cyclo- Benzyl Solubility Number hexanone2 acetate AMD810 (% w/w) @ 10° C. 1 0 0 1 3.3 34.3 2 0 0.2 0.8 4.3 32.3 3 0.2 0 0.8 4.5 33.9 4 0.2 0.2 0.6 6.2 32.9 5 0 0.4 0.6 6.5 33.1 6 0.2 0.4 0.4 10.5 32.1 7 0 0.6 0.4 11 32.1 8 0 0.8 0.2 12 26.6 9 0.13 0.62 0.25 not tested not tested 10 0.2 0.6 0.2 13.6 29.9 11 0 1 0 14.3 16.2 12 0.2 0.8 0 15.2 18.4

Example 3 Storage Stability of Representative Samples of the Described Fungicidal Composition

    • a) Accelerated storage stability study of Compound A in liquid compositions comprising benzyl acetate, AMD 810 and a third solvent.

The stability of Compound A in a variety of liquid compositions stored at 54° C. for 2 weeks is shown in Table 12. The test compositions were prepared in a manner similar to that described in Example 1 using one or more of Compound A, prothioconazole, pyraclostrobin, benzyl acetate, and AMD 810, and a third solvent chosen from cyclohexanone, acetophenone, 2-heptanone, 2-heptanol, oleyl alcohol or 2-ethylhexanol.

TABLE 12 Stability of Compound A in Liquid Compositions Comprising Benzyl Acetate, AMD 810 and a Third Solvent after Storage for 2 Weeks at 54° C. Compound Composition (wt %) A after Compound Prothio- Pyraclo- Benzyl AMD Third Storage (% A conazole strobin acetate 810 Solvent Third Solvent retention)1 4.9 — — 94.1 — — none 85  3.4 — — — 96.0 — none 49  12.0 — — — — 85.7 cyclohexanone 96  4.9 7.4 — 46.8 25.2 — none 912 4.9 — 5.0 48.4 26.0 — none 922 4.1 — 5.2 37.0 20.0 8.2 cyclohexanone 932 4.9 — 6.3 44.4 23.9 4.9 acetophenone 942 4.9 — 6.3 44.4 23.9 4.9 2-heptanone 932 4.9 — 6.3 44.4 23.9 4.9 oleyl alcohol 922 4.9 — 6.3 44.4 23.9 4.9 2-ethyl hexanol 962 4.9 — 6.3 44.4 23.9 4.9 2-heptanol 942 7.7 — 9.8 37.1 20.0 9.6 cyclohexanone 97  4.9 — 6.3 41.2 22.2 9.8 cyclohexanone 98  5.0 — 6.4 40.9 22.0 10.0 2-ethyl hexanol 95  7.8 — 9.9 36.7 19.8 9.7 2-ethyl hexanol 97  1Determined by HPLC analysis; 2Composition includes an emulsifier blend (14.7 wt %) comprising calcium dodecylbenzene sulfonate, butanol ethylene oxide/propylene oxide block polymer, and tridecyl alcohol ethoxylate.

Example 4 Storage Stability and Dilution of Sample 1 in Water

a) Storage Stability of Sample 1:

Sample 1 was stored at 54° C. for 2 weeks in a closed container. The sample remained as a clear, homogeneous yellow liquid with no solids formation or phase separation during the storage period. HPLC analysis showed 97.6% retention of Compound A after the storage period.

Sample 1 was stored at −10° C. for 1 week in a closed container following CIPAC Method 39.3. The sample remained as a clear homogeneous yellow liquid with no crystallization occurring.

Sample 1 was stored in a closed container at freeze-thaw conditions where the temperature was cycled between −10° C. and 40° C. every 24 hours for 4 weeks. The sample remained as a homogeneous liquid after storage.

b) Dilution of Sample 1 in Rt Water:

Following CIPAC Method 36.3, a 1 mL aliquot of Sample 1 was diluted in 100 mL of 342 ppm hardness water at room temperature to readily form a uniform, oil-in-water emulsion that maintained its stability at rt for at least 24 hours. No crystallization of Compound A was evident in the emulsion.

c) Dilution of Sample 1 in 5° C. Water:

Following CIPAC Method 36.3, a 1 mL aliquot of Sample 1 was diluted in 100 mL of 342 ppm hardness water at 5° C. to readily form a uniform, oil-in-water emulsion that maintained its stability at rt for at least 24 hours. No crystallization of Compound A was evident in the emulsion.

d) Storage Stability of Sample 6:

Sample 6 was stored at 54° C. for 2 weeks in a closed container. The sample remained as a clear, homogeneous yellow liquid with no solids formation or phase separation during the storage period. HPLC analysis showed 91% retention of Compound A after the storage period.

e) Storage Stability of Sample 7:

Sample 7 was stored at 54° C. for 2 weeks in a closed container. The sample remained as a clear, homogeneous yellow liquid with no solids formation or phase separation during the storage period. HPLC analysis showed 91% retention of Compound A after the storage period.

Example 5 Evaluation of the Described Fungicidal Compositions for Disease Control

a) Comparison of disease control using 3 EC formulations comprising active ingredient Compound A that differ in their water immiscible organic solvent composition.

Methods:

The fungicide formulations comprising Compound A were applied to wheat seedlings (2 leaf stage) with the use of a track sprayer (Devris) in a spray volume equal to 200 l/ha. Five concentrations of active ingredient were used. The concentrations used were 40.3, 13.4, 4.48 and 1.49 g ai/ha. Plants were inoculated in 3 day curative (3DC) and one day protectant (1DP) tests. Plants were challenged with both PUCCRT (Puccinia triticina; wheat brown rust) and SEPTTR (Septoria tritici; wheat leaf blotch) fungal pathogens. A total of 3 replications were used for each timing and pathogen combination. Disease caused by PUCCRT was evaluated 7 days after inoculation and disease caused by SEPTTR was evaluated 18-21 days after inoculation. The % tissue infected was determined and then the % disease control was calculated using the following equation: % disease control=(1-observed disease/disease from the untreated)*100.

Materials:

The emulsifiable concentrate (EC) formulations shown in Table 13 were used in fungicide spray applications for the control of Septoria tritici (wheat leaf blotch) and Puccinia triticina (wheat brown rust) on wheat plants. The Sample A and Sample B comparative formulations comprised of cyclohexanone/Aromatic 100 and N-methylpyrrolidone/Aromatic 200ND, respectively, as the water immiscible organic solvents, whereas the Sample C formulation comprised of benzyl acetate/N,N-dimethyl fatty acid amide as the water immiscible organic solvent.

TABLE 13 Composition of EC Formulations Used in Fungicide Spray Applications Formu- Conc. lation Type Component Role g/L Sam- EC Compound A Active Ingredient 70.0 ple A Tensiofix N9811HF Emulsifier 14 Tensiofix N9839HF Emulsifier 98 cyclohexanone Solvent 223.9 Aromatic 100 Solvent 527.1 Sam- EC Compound A Active Ingredient 100.0 ple B Sponto 300T Emulsifier 11 Sponto 500T Emulsifier 43 N-methyl pyrrolidone Solvent 423 Aromatic 200ND Solvent 423 Sam- EC Compound A Active Ingredient 50 ple C eo/po block copolymer Emulsifier 30 calcium dodecylbenzene Emulsifier 75 sulfonate tridecyl alcohol, ethoxylated Emulsifier 45 benzyl acetate Solvent 517.3 N,N-dimethyl fatty acid amide Solvent 287.7

Disease Control Data:

Table 14 shows the average disease control of fungicide spray applications for the control of Septoria tritici (SEPTTR; wheat leaf blotch) and Puccinia triticina (PUCCRT; wheat brown rust) on wheat plants.

TABLE 14 Disease Control on Wheat Plants with Various Spray Applied Formulations Comprising Compound A Pathogen and Compound A Application Rate (g ai/ha) Application 1.47 4.48 13.4 40.3 Formulation Applied Timing Average % Disease Control none - inoculated PUCCRT 1DP 0 0 0 0 none - clean PUCCRT 1DP 100 100 100 100 Sample A - comparative PUCCRT 1DP 17 27 97 99 Sample B - comparative PUCCRT 1DP 19 44 90 98 Sample C PUCCRT 1DP 50 90 99 100 Sample C + Trycol 5941 PUCCRT 1DP 80 99 100 100 none - inoculated PUCCRT 3DC 0 0 0 0 none - clean PUCCRT 3DC 100 100 100 100 Sample A - comparative PUCCRT 3DC 0 0 0 22 Sample B - comparative PUCCRT 3DC 0 0 0 18 Sample C PUCCRT 3DC 0 0 16 73 Sample C + Trycol 5941 PUCCRT 3DC 0 0 22 87 none - inoculated SEPTTR 1DP 0 0 0 0 none - clean SEPTTR 1DP 100 100 100 100 Sample A - comparative SEPTTR 1DP 21 19 59 67 Sample B - comparative SEPTTR 1DP 4 13 29 90 Sample C SEPTTR 1DP 17 45 97 100 Sample C + Trycol 5941 SEPTTR 1DP 47 83 91 96 none - inoculated SEPTTR 3DC 0 0 0 0 none - clean SEPTTR 3DC 100 100 100 100 Sample A - comparative SEPTTR 3DC 86 93 95 97 Sample B - comparative SEPTTR 3DC 75 87 88 97 Sample C SEPTTR 3DC 71 93 100 100 Sample C + Trycol 5941 SEPTTR 3DC 90 100 100 100 1Trycol 5941 (BASF; tridecyl alcohol-(EO)9) is an adjuvant added to the respective spray solutions at a concentration of 0.05 wt % to boost fungicide efficacy.

b) Disease control using described compositions comprising Compound A and, optionally, either prothiconazole or pyraclostrobin, before and after a simulated rain event to evaluate rainfastness of the applied compositions.

Methods:

‘Yuma’ wheat was used as the host plant in these fungicide efficacy trials. Seedlings were sprayed when the second leaf was fully expanded (8 days after seeding). The fungus Puccinia triticina (PUCCRT; wheat brown rust) was used as the test organism in the efficacy bioassay. The amount of rain applied after fungicide applications was 10 mm. Four separate rain treatments were used with each fungicide treatment. The rain treatments were no rain, and rain at 1, 30, or 60 minutes after fungicide application. There were three replicate for each combination of fungicide, rate, and rainfall interval. All fungicide formulations were diluted in water to achieve the desired spray concentrations. Fungicides were applied with a track sprayer set at 150 liters per hectare delivery volume at 2.1 atm and a speed of 1.9 km/h. A flat fan TeeJet 8003 nozzle tip was used. The nozzle tip was 50 cm above the top of the seedlings. All fungicide formulations were applied at ¼, ⅛ and 1/16 of the recommended field rate (1X). Table 15 shows the results from these trials.

TABLE 15 Disease Control on Wheat Plants with Various Spray Applied Formulations Comprising Compound A after Simulated Rain Events % Disease Control of Active For- PUCCRT 1DP at Indi- Ingredient mula- cated Rate of Application1 (1X Rate) tion Weather event ¼X ⅛X 1/16X Compound A Sam- no rain 100 100 98 (130 g ai/ha) ple 1 rain at 1 minute 100 99 95 rain at 30 minutes 100 98 92 rain at 60 minutes 100 98 92 Compound A + Sam- no rain 100 100 99 prothioconazole ple 2 rain at 1 minute 100 99 91 (100 + 200 rain at 30 minutes 100 96 81 g ai/ha) rain at 60 minutes 100 97 91 Compound A + Sam- no rain 100 100 89 prothioconazole ple 4 rain at 1 minute 100 99 61 (100 + 200 rain at 30 minutes 100 98 56 g ai/ha) rain at 60 minutes 100 99 50 Compound A + Sam- no rain 100 100 99 pyraclostrobin ple 5 rain at 1 minute 100 100 83 (100 + 125 rain at 30 minutes 100 100 90 g ai/ha) rain at 60 minutes 100 99 89 1The application rate for each active ingredients are ¼, ⅛, and 1/16, respectively, of the X rate shown in column 1 for the respective active ingredient.

The entire disclosures of (1) PCT Patent Application No. PCT/US15/68011, filed Dec. 30, 2015, titled FUNGICIDAL COMPOSITIONS; (2) PCT Patent Application No. PCT/US15/68018, filed Dec. 30, 2015, titled FUNGICIDAL COMPOSITIONS; and (3) PCT Patent Application No. PCT/US15/68019, filed Dec. 30, 2015, titled FUNGICIDAL COMPOSITIONS are expressly incorporated herein by reference.

The present invention is not limited in scope by the embodiments disclosed herein which are intended as illustrations of a few aspects of the invention and any embodiments which are functionally equivalent are within the scope of this invention. Various modifications of the processes, methods, and compositions in addition to those shown and described herein will become apparent to those skilled in the art and are intended to fall within the scope of the appended claims. Further, while only certain representative combinations of the process and method steps and composition components disclosed herein are specifically discussed in the embodiments above, other combinations of the composition components and process and method steps will become apparent to those skilled in the art and also are intended to fall within the scope of the appended claims. Thus a combination of components or steps may be explicitly mentioned herein; however, other combinations of components and steps are included, even though not explicitly stated. The term comprising and variations thereof as used herein is used synonymously with the term including and variations thereof and are open, non-limiting terms.

Claims

1. A method of controlling fungal plant pathogens or diseases comprising the steps of contacting the vegetation or an area adjacent thereto to prevent the growth of the fungal pathogens or diseases with a fungicidally effective amount of a fungicidal composition comprising:

a) a fungicidal compound of Formula
b) at least one ionic surfactant;
c) at least one nonionic surfactant;
d) at least one acetate ester;
e) at least one N,N-dialkylcarboxamide; and
f) at least one of a ketone and an alcohol.

2. The method of claim 1, wherein the fungicidal composition includes from about 1 gram per liter (g/L) to about 200 g/L of the fungicidal compound of the Formula

3. The method of claim 1, wherein the fungicidal composition includes from about 1 g/L to about 100 g/L of at least one ionic surfactant, wherein the at least one ionic surfactant includes at least one anionic surfactant.

4. The method of claim 1, wherein the fungicidal composition includes from about 1 g/L to about 200 g/L of the at least one nonionic surfactant.

5. The method of claim 1, wherein the fungicidal composition includes from about 50 g/L to about 700 g/L of the at least one acetate ester.

6. The method of claim 1, wherein the fungicidal composition includes from about 25 g/L to about 300 g/L of the at least one N,N-dialkylcarboxamide, wherein the at least one N,N-dialkylcarboxamide includes an N,N-dimethyl fatty acid amide.

7. The method of claim 1, wherein the fungicidal composition includes from about 25 g/L to about 150 g/L of the at least one of a ketone and an alcohol.

8. The method of claim 1, wherein the fungicidal composition includes the at least one acetate ester, the at least one N,N-dialkylcarboxamide and the at least one of the ketone and the alcohol together form a water immiscible organic solvent.

9. The method of claim 1, wherein the weight ratios of the at least one acetate ester:the at least one N,N-dialkylcarboxamide:the at least one of the ketone and the alcohol range from about 1-10:1-10:1-10.

10. The method of claim 1, wherein the weight ratios of the at least one acetate ester:the N,N-dialkylcarboxamide:the at least one of the ketone and the alcohol range from about 4-6:1-3:1-2.

11. The method of claim 1, wherein the at least one acetate ester is selected from a group consisting of benzyl acetate, cyclohexylmethyl acetate and phenyl acetate.

12. The method of claim 1, wherein the at least one N,N-dialkylcarboxamide is selected from a group consisting of N,N-dimethylhexanamide, N,N-dimethyloctanamide, N,N-dimethyldecanamide and N,N-dimethyldodecanamide.

13. The method of claim 1, wherein the at least one of the ketone and the alcohol is selected from a group consisting of acetophenone, cyclohexanone, 2-ethylhexanol and 2-heptanol.

14. The method of claim 1, wherein the water immiscible organic solvent includes benzyl acetate, one or more than one of a fatty acid N,N-dialkylcarboxamide and cyclohexanone.

15. The method of claim 1, wherein fungicidal composition further comprising at least one additional fungicidal compound.

16. The method of claim 15, wherein the at least one additional fungicidal compound is selected from a group consisting of azoxystrobin, bifujunzhi, coumethoxystrobin, coumoxystrobin, dimoxystrobin, enestroburin, enoxastrobin, fenaminstrobin, fenoxystrobin, flufenoxystrobin, fluoxastrobin, jiaxiangjunzhi, kresoxim-methyl, mandestrobin, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyrametostrobin, pyraoxystrobin, triclopyricarb, trifloxystrobin, methyl 2-[2-(2,5-dimethylphenyloxymethyl)phenyl]-3-methoxyacrylate, azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, oxpoconazole, paclobutrazole, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, uniconazole, imazalil, pefurazoate, prochloraz, triflumizole, pyrimidines, fenarimol, nuarimol, pyrifenox, and triforine.

17. The method of claim 1, wherein the fungal plant pathogens include Septoria tritici, Puccinia triticina, Mycosphaerella graminicola, Puccinia triticina, Puccinia striiformis, Venturia inaequalis, Ustilago maydis, Uncinula necator, Rhynchosporium secalis, Leptosphaeria nodorum, Magnaporthe grisea, Monilinia fructicola, Pseudoperonospora cubensis, Pseudocercosporella herpotrichoides, Phakopsora pachyrhizi, Phaeosphaeria nodorum, Blumeria graminis tritici, Blumeria graminis hordei, Erysiphe cichoracearum, Ezysiphe graaminis, Glomerella lagenarium, Cercospora beticola, Alternaria solani, Rhizoctonia solani, Plasmopara viticola, Phytophthora infestans, Pyricularia oryzae, and Pyrenophora teres.

18. The method of claim 1, wherein the fungal plant diseases include anthracnose, blasts, botrytis, brown rust, blister smut, brown rot, downy mildew, fusarium, powdery mildew, rusts, glume blotch, leaf blotch, net blotch, sheath blight, stripe rust, scab, eye spot, leaf spot, early blight, and late blight.

19. The method of claim 1, wherein the at least one ionic surfactant is an anionic surfactant selected from a group consisting of an alkali, alkaline earth and ammonium salt of an alkylarylsulfonic acid.

20. The method of claim 1, wherein the at least one nonionic surfactant is selected from a group consisting of an alcohol initiated EO/PO block copolymer and an alcohol ethoxylate.

Patent History
Publication number: 20160183527
Type: Application
Filed: Dec 30, 2015
Publication Date: Jun 30, 2016
Inventors: Derek J. Hopkins (New Plymouth), Cheryl Ann Cathie (New Plymouth), Todd Mathieson (Indianapolis, IN), Neil Foster (Drusenheim)
Application Number: 14/984,152
Classifications
International Classification: A01N 43/40 (20060101); A01N 43/56 (20060101); A01N 43/653 (20060101);