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Dowelanco Patents
Assignee:
Dowelanco
Address:
Indianapolis, IN
No. of patents:
139
Patents:


1 2 3


Patent Number Title Of Patent Date Issued
6370812 Methods, systems and baits for detecting and controlling termites April 16, 2002
The subject invention pertains to materials and methods useful for management of certain pests. The invention is particularly well suited for the control of social insect pests and, particularly, termites. The invention concerns unique toxicant-containing matrices as well as apparatu
6350934 Nucleic acid encoding delta-9 desaturase February 26, 2002
The present invention relates to nucleic acid molecules encoding delta 9 desaturase gene, and expression vectors, plant cells, and transgenic plants expressing delta 9 desaturase nucleic acid. The nucleic acid molecules of the present invention can be used, for example, to decrease d
5840861 A83543 compounds and process for production thereof November 24, 1998
New A83543 components, including fermentation products A83543K, A835430, A83543P, A83543U, A83543V, A83543W and A83543Y and N-demethyl derivatives, and salts thereof, are useful for the control of insects and mites. The pseudoaglycones of the new A83543 components are useful for the
5743477 Insecticidal proteins and method for plant protection April 28, 1998
The present invention provides a composition and method of using plant non-specific lipid acyl hydrolases to protect plants otherwise susceptible to insect infestation by one or more of corn rootworms, potato beetles, armyworms, borers, cutworms, wireworms, earworms and aphids.
5700940 N-aryl[1,2,4]triazolo[1,5-a]pyridine-2-sulfonamide herbicides December 23, 1997
Substituted N-aryl[1,2,4]triazolo[1,5-a]pyridine-2-sulfonamide compounds, such as N-(2,6-difluorophenyl)-5-methoxy-7-methyl[1,2,4]triazolo[1,5-a]pyridine-2- sulfonamide, N-(4-bromo-1-methyl-3-pyrazolyl)-8-chloro-5-methoxy[1,2,4]triazolo[1,5-a]p yridine-2-sulfonamide, and N-(2-f
5691383 Use of hexaflumuron as a termiticide November 25, 1997
Method of using specific acyl urea compounds as termiticides. The compounds are unusually non-repellant to termites and active at low dosages.
5688953 Process for the preparation of 3,3,5-trichloroglutarimide November 18, 1997
3,3,5-Trichloroglutarimide is prepared by combining 4-cyano-2,2,4-trichlorobutanoyl chloride with water in an inert organic solvent at a temperature between about 20.degree. C. and about 50.degree. C. to obtain a mixture of 3,3,5-trichloroglutarimide and 3,3,5,6-tetrachloro-5,6-dihyd
5670486 A83543 compounds and process for production thereof September 23, 1997
New A83543 components, including fermentation products A83543K, A83543O, A83543P, A83543U, A83543V, A83543W and A83543Y and N-demethyl derivatives, and salts thereof, are useful for the control of insects and mites. The pseudoaglycones of the new A83543 components are useful for the
5670364 A83543 compounds and process for production thereof September 23, 1997
New A83543 components, including fermentation products A83543K, A835430, A83543P, A83543U, A83543V, A83543W and A83543Y and N-demethyl derivatives, and salts thereof, are useful for the control of insects and mites. The pseudoaglycones of the new A83543 components are useful for the
5665595 Immunoglobulins against insect tissue September 9, 1997
The present invention provides a composition and method of protecting plants otherwise susceptible to infestation by insects of the orders Lepidoptera and Coleoptera.
5646026 Ribosome-inactivating proteins, inactive precursor forms thereof, a process for making and a met July 8, 1997
The present invention is directed to a ribosome inactivating proteins. The proteins are characterized by being in a single chain proRIP inactive form that can be converted into an active form by cleavage with proteases.
5635384 Ribosome-inactivating proteins, inactive precursor forms thereof, a process for making and a met June 3, 1997
The present invention is directed to a ribosome inactivating proteins. The proteins are characterized by being in a single chain proRIP inactive form that can be converted into an active form by cleavage with proteases.
5631155 Saccharopolyspora spinosa strain May 20, 1997
New A83543 components, including fermentation products A83543Q, A83543R, A83543S and A83543T and N-demethyl derivatives, and salts thereof, are useful for the control of insects and mites. The pseudoaglycones are useful for the preparation of A83543 components. Methods for making the
5622915 Method of using triclopyr to increase fruit size or quality or maturation rate April 22, 1997
A method for regulating plant growth which comprises applying to a fruit bearing plant an amount of 3,5,6-trichloro-2-pyridyloxyacetic acid (i.e., triclopyr) or a lower (C.sub.1-10) alkyl ester or salt thereof that is nonphytotoxic and effective to provide increased fruit size or quality
5614469 N-pyridinyl[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonamide herbicides March 25, 1997
Substituted N-pyridinyl[1,2,4]triazolo[1,5-c]-pyrimidine-2-sulfonamide compounds, such as N-(2-fluoro-4-methyl)-7-fluoro-5-methoxy[1,2,4]triazolo[1,5-c]pyrimidine-2 -sulfonamide, were prepared bycondensation of a 2-chlorosulfonyl[1,2,4]triazolo[1,5-c]pyrimidine compound, such as 2
5602075 N-aryl[1,2,4]triazolo[1,5-a]pyrazine-2-sulfonamide herbicides February 11, 1997
Substituted N-aryl[1,2,4]triazolo[1,5-a]-pyrazine-2-sulfonamide compounds, such as 5-bromo-N-(2,6-dichlorophenyl)-8-methoxy[1,2,4]triazolo[1,5-a]-pyrazine-2- sulfonamide, were prepared by condensation of a substituted 2-chlorosulfonyl[1,2,4]triazolo[1,5-a]pyrazine compound, such as
5597836 N-(4-pyridyl) (substituted phenyl) acetamide pesticides January 28, 1997
N-(4-Pyridyl) arylacetamides, for example N-((3-chloro-2-ethyl)-4-pyridyl)(4-(4-chlorophenoxy)phenyl)-acetamide, and 4-(aralkyoxy or aralkylamino)pyridines, for example 4-[2-[4-(2,2,2-trifluoroethoxy)phenyl]ethoxy]pyridine, are active against nematodes, insects, mites, and plant path
5591606 Process for the production of A83543 compounds with Saccharopolyspora spinosa January 7, 1997
New A83543 components, including fermentation products A83543Q, A83543R, A83543S and A83543T and N-demethyl derivatives, and salts thereof, are useful for the control of insects and mites. The pseudoaglycones are useful for the preparation of A83543 components. Methods for making the
5576187 Standards for phosphorothioate insecticide immunoassays November 19, 1996
Improvements in immunoassays for chlorpyrifos and compounds structurally related to chlorpyrifos are achieved by using standards of increased stability.
5571901 Insecticide and miticide compositions containing A83543 compounds November 5, 1996
Fermentation product A83543, comprising major components A83543A and A83543D and minor components A83543B, A83543C, A83543E, A83543F, A83543G, A83543H and A83543J, is produced by a newly described species, Saccharopolyspora spinosa. The A83543 components and their acid-addition salts
5571775 N-aryl[1,2,4]triazolo[1,5-a]pyridine-2-sulfonamide herbicides November 5, 1996
Substituted N-aryl[1,2,4]triazolo[1,5-a]pyridine-2-sulfonamide compounds, such as N-(2,6-difluorophenyl)-5-methoxy-7-methyl[1,2,4]triazolo[1,5-a]pyridine-2- sulfonamide, N-(4-bromo-1-methyl-3-pyrazoly)-8-chloro-5-methoxy[1,2,4]triazolo[1,5-a]py ridine-2-sulfonamide, and N-(2-fl
5563269 2-alkoxy-4-hydrazinopyrimidine compounds and their use in the preparation of 5-alkoxy-1,2,4-tria October 8, 1996
5-Alkoxy-1,2,4-triazolo[4,3-c]pyrimidine-3(2H)-thione compounds, such as 5-ethoxy-8-fluoro-1,2,4-triazolo[4,3-c]pyrimidine-3(2H)-thione, were prepared by cyclization of 2-alkoxy-4-hydrazinopyrimidine compounds, such as 2-ethoxy-5-fluoro-4-hydrazinopyrimidine, with carbon disulfide and
5560909 Insecticidal compositions and process for preparation thereof October 1, 1996
The invention concerns certain insecticidal compositions of ingestible insecticides selected from the group consisting of DNA viruses, RNA viruses and bacteria of the order Bacillus such as, for example, Bacillus thuringiensis var. israelensis entrapped by a suitable charged polymer.
5556883 Use of hexaflumuron as a termiticide September 17, 1996
Method of using specific acyl urea compounds as termiticides. The compounds are unusually non-repellant to termites and active at low dosages.
5556859 N-(4-pyrimidinyl)amide pesticides September 17, 1996
N-(4-Pyrimidinyl)amide pesticides of the formulas ##STR1## and N-oxides and salts thereof, wherein the variable groups are as defined in the specification, are active against nematodes, insects, mites, and plant pathogens.
5552546 Process for the preparation of 2-ethoxy-4,6-dihydroxypyrimidine September 3, 1996
A salt of 2-ethoxy-4,6-dihydroxypyrimidine (DHEP) is prepared by contacting a salt of O-ethylisourea with dimethyl malonate in the presence of a methoxide base to form the salt of DHEP. The salt of DHEP can optionally be protonated with an acid to form neutral DHEP. The reaction is typic
5539089 A83543 aglycones and pseudoglycones July 23, 1996
A83543 Aglycones A83543AgA, A83543AgD, A83543AgE, and A83543AgF, and A83543 pseudoaglycones A83543PsaA2, A83543PsaB2, A83543PsaD2, and A83543PsaN2 are intermediates useful in preparation of known insecticides.
5508035 Stable concentrates and emulsions of water-insoluble organic pesticides April 16, 1996
Stable emulsions of water-insoluble organic pesticides are formed by mixing the pesticide with an aqueous dispersion of a graft copolymer comprising a reactive polymeric surfactant base polymer and a nonionic hydrophobic grafted composition. The graft copolymer spontaneously absorbs orga
5502235 Solventless process for making 2,6 difluorobenzonitrile March 26, 1996
A process for making 2,6-difluorobenzonitrile, comprising reacting 2,6-dichlorobenzonitrile with a substantially anhydrous metal fluoride at a temperature between about 160.degree. C. and about 300.degree. C. and in the presence of a phase transfer catalyst, which is typically a polyethe
5498773 Herbicidal compositions with increased crop safety March 12, 1996
Disclosed are herbicidal concentrate formulation compositions having reduced grass crop plant phytotoxicity comprising certain sulfonamide or sulfonylurea herbicides in admixture with a non-herbicidal organic or inorganic acid or mixture thereof in an amount sufficient to insure that
5496931 Insecticide and miticide A83543 compounds and their method of production by fermentation March 5, 1996
Fermentation product A83543, comprising major components A83543A and A83543D and minor components A83543B, A83543C, A83543E, A983543F, A83543G, A83543H and A83543J, is produced by a newly described species, Saccharopolyspora spinosa. The A83543 components and their acid-addition salt
5494887 Ring annulated 5-alkoxy-n-aryl[1,2,4]triazolo[1,5-C]-pyrimidine-2-sulfonamide herbicides February 27, 1996
Substituted ring annulated 5-alkoxy-N-aryl-[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonamide compounds, such as N-(2,6-dichlorophenyl)-5-methoxycyclopenteno[d]-[1,2,4]triazolo[1,5-c]pyri midine-2-sulfonamide, were prepared by condensation of an appropriate 2-chloro-sulfonyl-5-alkoxy[
5493024 3,4,N-trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamides and their use as insectioides February 20, 1996
3,4,N-triaryl-4,5-dihydro-1H-pyrazole-1-carboxamide compounds having an aryl moiety in the 4-position that is an optionally substituted pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or quinolinyl moiety and aryl moieties in the 3-position and the N-position that are optionally subs
5488109 5-alkoxy[1,2,4]triazolo[1,5-c]pyrimidine-2(3H)--thione compounds and their use in the preparatio January 30, 1996
2-Chlorosulfonyl-5-alkoxy[1,2,4]triazolo-[1,5-c]pyrimidine compounds, such as 2-chlorosulfonyl-5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidine, that are useful for the preparation of 5-alkoxy[1,2,4]triazolo [1,5-c]pyrimidine-2-sulfonamide herbicides, were prepared in an improved ma
5488052 Aqueous flowable fenazaquin composition comprising sodium naphthalene formaldehyde condensates January 30, 1996
The present invention relates to a novel aqueous flowable composition of fenazaquin. It was found that conventional aqueous flowable formulations resulted in a product that lost miticidal activity during storage. The low miticidal activity was found to be due to an unacceptable level of
5486516 Furopyrimidine derivatives January 23, 1996
Pesticidal compounds of the formula (1) ##STR1## R.sup.1 is H, C.sub.1 -C.sub.4 alkyl, or phenyl optionally substituted with halo, (C.sub.1 -C.sub.4) alkyl, (C.sub.1 -C.sub.4) alkoxy, halo (C.sub.1 -C.sub.4) alkyl, or halo (C.sub.1 -C.sub.4) alkoxy;R.sup.2 is H, (C.sub.1 -C.sub.4) al
5480991 2-Alkoxy-4-hydroazinopyrimidine compounds and their use in the preparation of 5-alkoxy-1,2,4-tri January 2, 1996
5-Alkoxy[1,2,4]triazolo[1,5-c]pyrimidine-2 (3H)-thione compounds, such as 5-ethoxy-8-fluoro[1,2,4]triazolo[1,5-c]pyrimidine-2(3H)-thione, were prepared by treatment of a 5-alkoxy-1,2,4-triazolo-[4,3-c]pyrimidine-3(2H)-thione compound, such as 5-ethoxy-8-fluoro-1,2,4-triazolo[4,3-c]py
5466659 Triclopyr butoxyethyl ester compositions comprising vegetable oil esters as carriers November 14, 1995
This invention relates to novel triclopyr butoxyethyl ester (triclopyr BEE) compositions comprising the use of esters of vegetable oils as carriers in triclopyr BEE compositions for use in the control of undesirable vegetation. The present invention further relates to a method for co
5466659 Triclopyr butoxyethyl ester compositions comprising vegetable oil esters as carriers November 14, 1995
This invention relates to novel triclopyr butoxyethyl ester (triclopyr BEE) compositions comprising the use of esters of vegetable oils as carriers in triclopyr BEE compositions for use in the control of undesirable vegetation. The present invention further relates to a method for co
5461824 Method for controlling tree growth October 31, 1995
Tree growth is suppressed by placing an implant below the bark layer of the tree at each of a plurality of sites spaced around the circumference of the trunk of the tree, each implant containing a unit dose of active ingredient selected from flurprimidol, paclobutrazol, and uniconazole.
5461161 N-pyridinyl[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonamide herbicides October 24, 1995
Substituted N-pyridinyl[1,2,4]triazolo[1,5-c]-pyrimidine-2-sulfonamide compounds, such as N-(2-fluoro-4-methyl)-7-fluoro-5-methoxy[1,2,4]triazolo[1,5-c]pyrimidine-2 -sulfonamide, were prepared by condensation of a 2-chlorosulfonyl[1,2,4]triazolo[1,5-c]pyrimidine compound, such as
5461153 2-alkoxy-4-hydrazinopyrimidine compounds October 24, 1995
5-Alkoxy-1,2,4-triazolo[4,3-c]pyrimidine-3(2H)-thione compounds, such as 5-ethoxy-8-fluoro-1,2,4-triazolo[4,3-c]pyrimidine-3(2H)-thione, were prepared by cyclization of 2-alkoxy-4-hydrazinopyrimidine compounds, such as 2-ethoxy-5-fluoro-4-hydrazinopyrimidine, with carbon disulfide and
5447960 Fungicidal use of phenolic aromatic compounds September 5, 1995
A plant fungicide method comprises applying to the locus of a plant pathogen a fungicidally effective amount of a compound of formula (I) ##STR1## or a salt or a complex thereof, wherein: R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, and R.sup.8 are independently H,
5447905 N-indazolyl[1,2,4]triazolo[1,5-C]pyrimidine-2-sulfonamide herbicides September 5, 1995
Substituted N-indazolyl[1,2,4]triazolo[1,5]-c-pyrimidine-2-sulfonamide compounds, such as N-(4-fluoro-1-methyl-3-indazolyl)-5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]p yrimidine-2-sulfonamide, were prepared by condensation of a 2-chlorosulfonyl[1,2,4]triazolo[1,5-c]pyrimidine compound, s
5436223 Argricultural formulations comprising fluroxypyr esters which are liquid at 25.degree. C. July 25, 1995
Agricultural formulations of fluroxypyr that contain an ester of fluroxypyr that is liquid at ambient temperatures, such as the 1-butoxy-2-propyl ester or the 2-ethylhexyl ester, and that contain a reduced amount of organic solvent or no organic solvent are disclosed. The formulations ha
5424278 Hydroxycornexistin June 13, 1995
Hydroxycornexistin (1), the free dibasic acid thereof (2) ##STR1## agronomically acceptable bis-ester, monoester, monoamide, and monothioesters thereof, and agronomically acceptable salts thereof are selective herbicides for broad spectrum broadleaf and grass weed control in corn
5418247 3,4,N-trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamides and their use as insecticides May 23, 1995
3,4,N-Trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamide compounds wherein the substituent in the 4-position is a 5-membered heterocyclic ring moiety containing one ring oxygen or sulfur atom and one or two ring nitrogen atoms and the substituents in the 3-posit ion and the N-position
5411963 Quinazoline derivatives May 2, 1995
Substituted quinazolines of the formula (1): ##STR1## wherein: R.sup.1 to R.sup.4 are independently H, halo, (C.sub.1 -C.sub.4) alkyl, branched (C.sub.3 -C.sub.4) alkyl, halo (C.sub.1 -C.sub.4) alkyl, (C.sub.1 -C.sub.4) alkoxy, NO.sub.2, or NH.sub.2,provided thatat least two of R.sup
5410065 Preparation of 5-cylamino-1,2,4-triazole-3-sulfonamides April 25, 1995
5-Acylamino-1,2,4-triazole-3-sulfonamides, which are useful intermediates for the preparation of 1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide herbicides are prepared from 5-amino-3-mercapto-1,2,4-triazole by sequential acylation to 5-acylamino-3-mercapto-1,2,4-triazoles, chlorinatio
5406744 Bait station April 18, 1995
A bait station comprises a base having first and second side walls connected together along a corner and extending preferably at about a 90.degree. angle to one another, and a cover secured to the side walls to form a triangular unit. A pair of mutually-facing, C-shaped projections e
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