Basf Aktiengesellschaft

Basf Se Corporation

Basf Agrochemical Products B.v.

Reinhard, Robert

Hamprecht, Gerhard

Puhl, Michael

Seitz, Werner

Robert Reinhard

Gerhard Hamprecht

Cyrill Zagar

Olaf Menke

Helmut Walter

Karl-Otto Westphalen

Michael Puhl

Matthias Witschel

Markus Menges

Martina Otten

Peter Sch&auml;fer

Werner Seitz

Bernd Wolf

Bernd Sievernich

Liliana Parra Rapado

Michael Keil

Norbert Götz

William Karl Moberg

Thomas Ehrhardt

Michael Rack

Ulf Misslitz

Trevor William Newton

Thomas Seitz

Guido Mayer

Andreas Landes

Thomas Schmidt

Joachim Gebhardt

Matthias Bratz

Karsten Koerber

Peter Erk

Gerhard Cox

Juergen Langewald

Markus Gewehr

Peter Plath

Thomas Zierke

Norbert Gotz

Klaus Kreuz

Klaus Grossmann

Sebastian Soergel

Anja Simon

Richard R Evans

Julia Major

Timo Frassetto

Ingo Sagasser

Frank Stelzer

Klaus Groβmann

Eike Hupe

Andrea Vescovi

Tatjana Sikuljak

Toralf Kühn

Heidi Emilia Saxell

Tiziana Chiodo

Pascal Bindschaedler

Dschun Song

Jan Hendrik Wevers

Sandra Löhr

Alfred Michel

Stefan Scherer

Rex A Liebl

Tao Qu

Clark Klein

Thorsten Volk

Ricarda Niggeweg

Christian Pilger

Robert Brian Jones

Helmut Schiffer

Alejandro Arevalo

Peter M&uuml;nster

Annegret Scannell-Lansky

Christy Jones

Rex Liebl

Kenneth Scott Brown

Klaus Daeschner

Ulf Mißlitz

Klaus GROßMANN

Pesticidal mixtures comprising as active compounds 1) 1-[(1RS)-1,2-dimethylpropyl]-N-ethyl-5-methyl-N-pyridazin-4-yl-1H-pyrazole-4-carboxamide and 2) at least one further compound B selected from B.1) Succinate dehydrogenase inhibitors as defined in the specification; B.2) Inhibitors of oxysterol binding protein as defined in the specification; B.3) Inhibitors of complex III at Qi site selected from: a) florylpicoxamid, and b) fenpicox-amid; B.4) Strobilurins as defined in the specification; B.5) Inhibitors of C14-demethylase in sterol biosynthesis as defined in the specification; B.6) Inhibitors of cell division and cytoskeleton as defined in the specification, B.7) Other compounds of unknown mode of action as defined in the specification; and B.8) N-[[2-fluoro-4-[(2S,3S)-2-hydroxy-3-(3,4,5-trichlorophenyl)-3-(trifluoromethyl)pyrrolidin-1-yl]phenyl]methyl]cyclopropanecarboxamide; wherein component 1) and component 2) are present in a weight ratio of from 1000:1 to 1:1000; methods and use of these mixtures for combating invertebrate pests such as insects, arachnids, nematodes and/or harmful fungi in and on plants, and for protecting such plants being infested with pests and/or harmful fungi.

Pesticidal mixtures comprising a pyrazole compound

Pesticidal mixtures including a pesticidally active compound I selected from:  

Pesticidally active mixtures

Pesticidal mixtures including a pesticidally active anthranilamide compound of formula (I) and at least one further pesticidal active ingredient. The pesticidal mixtures are useful for combating and controlling insects, acarids or nematodes in and on plants, and for protecting such plants being infested with pests.

Pesticidally activi mixtures comprising anthranilamide compounds

Methods and uses for controlling non-crop pests (especially of the orders Blattodea, Diptera, Hemiptera, Hymenoptera, Isoptera, Orthoptera) and/or populations of social insects and non-social solitary or gregarious insects, especially ants, wasps, termites and cockroaches, with a carboxamide compound and its mixtures, and compositions comprising it, are disclosed.

Method for controlling non-crop pests

Described herein are agricultural methods for controlling pests on and/or increasing the plant health of a cultivated plant, with at least one modification, using a pesticidal carboxamide compound or a mixtures thereof. In particular, methods of controlling harmful insects, which are resistant to an insecticidal trait of the plant, are provided. In addition, the use of a pesticidal carboxamide compound or mixtures thereof for protecting a plant, plant propagation material, seeds or the locus of growth, against the attack or infestation by pests, wherein the plant has been modified by mutagenesis or genetic engineering, and for controlling pests that are resistant to an insecticidal trait of the plant are described.

Use of an insecticidal carboxamide compound against pests on cultivated plants

The present invention relates to a novel crystalline form A of 1,5-dimethyl-6-thioxo-3-(2,2,7-trifluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-1,3,5-triazinane-2,4-dione. The invention also relates to a process for the production of this crystalline form and formulations for plant protection which contains the novel crystalline form of 1,5-dimethyl-6-thioxo-3-(2,2,7-trifluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-1,3,5-triazinane-2,4-dione.

Crystalline form A of 1,5-dimethyl-6-thioxo-3-(2,2,7-trifluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[B][1,4]oxazin-6-yl)-1,3,5-triazinane-2,4-dione

The present invention relates to a novel crystalline form B of 1,5-dimethyl-6-thioxo-3-(2,2,7-trifluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-1,3,5-triazinane-2,4-dione The invention also relates to a process for the production of this crystalline form and formulations for plant protection which contains the novel crystalline form of 1,5-dimethyl-6-thioxo-3-(2,2,7-trifluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-1,3,5-triazinane-2,4-dione.

Crystalline form B of 1,5-dimethyl-6-thioxo-3-(2,2,7-trifluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[B][1,4]oxazin-6-yl)-1,3,5-triazinane-2,4-dione

Herbicidal compositions based on 3-phenyluracils and 3-sulfonylisoxazolines

A process for preparing phenyl iso(thio)cyanates of the formula I in which a compound of the formula II or its HCl adduct is reacted with a phosgenating agent where W is oxygen or sulfur and Ar and A are as defined in claimis described. Moreover, the invention relates to the use of the phenyl iso(thio)cyanates for preparing crop protection agents.

Bifunctional phenyl iso(thio)cyanates, processes and intermediates products for their preparation

The invention relates to the use of piperazine compounds of formula (I) or the agriculturally useful salts of piperazine compounds of formula (I) as herbicides, the variables in formula (I) being defined as cited in the claims and the description. 

Piperazine compounds with a herbicidal action

The present invention relates to a crystalline form of 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)pyrimidinyl]-4-fluoro-N-[[methyl(1-methylethyl)-amino]sulfonyl]benzamide. The invention also relates to a process for the preparation of this crystalline form and to plant protection formulations which comprise this crystalline form of the phenyluracil.

Crystalline form of 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)-pyrimidinyl]-4-fluoro-N-[[methyl(1-methyl-ethyl)amino]sulfonyl]benzamide

The present invention relates to hydrates of 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)pyrimidinyl]-4-fluoro-N-[[methyl(1-methylethyl)amino]-sulfonyl]benzamide. The invention also relates to a process for the preparation of these hydrates and to plant protection formulations which comprise hydrates of the phenyluracil I.

Hydrates of 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)-pyrimidinyl]-4-fluoro-N-[[methyl(1-methylethyl)amino]sulfonyl]benzamide

Substituted pyridines of the formula I in which the variables are defined according to the description, their agriculturally suitable salts, processes and intermediates for preparing the pyridines of the formula I, compositions comprising them and their use as herbicides, i.e. for controlling harmful plants, and also a method for controlling unwanted vegetation which comprises allowing a herbicidally effective amount of at least one pyridine compound of the formula I to act on plants, their seed and/or their habitat.

Substituted pyridines having a herbicidal effect

Bifunctional phenyl ISO (THIO) cyanates, processes and intermediates for their preparation

The present invention relates to heteroaroyl-substituted serinamides of the formula (I) in which the variables A and Rto Rare as defined in the description,

Heteroaroyl-substituted serine amides

Growing community of inventors

Ludwigshafen, Germany

Robert Reinhard