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WO2016091675A1 - Procédé d'amélioration de la santé de plante - Google Patents

Procédé d'amélioration de la santé de plante Download PDF

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Publication number
WO2016091675A1
WO2016091675A1 PCT/EP2015/078334 EP2015078334W WO2016091675A1 WO 2016091675 A1 WO2016091675 A1 WO 2016091675A1 EP 2015078334 W EP2015078334 W EP 2015078334W WO 2016091675 A1 WO2016091675 A1 WO 2016091675A1
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WO
WIPO (PCT)
Prior art keywords
plant
methyl
phenyl
tetrazol
plants
Prior art date
Application number
PCT/EP2015/078334
Other languages
English (en)
Inventor
Jurith Montag
Markus Gewehr
Original Assignee
Basf Se
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Basf Se filed Critical Basf Se
Publication of WO2016091675A1 publication Critical patent/WO2016091675A1/fr

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/713Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms

Definitions

  • the present invention relates to a method for improving the health of a plant, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of an active ingredient, selected from the group of compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12:
  • Healthier plants are desirable since they result among others in better yields and/or a better quality of the plants or crops. Healthier plants also better resist to biotic and/or abiotic stress. A high resistance against biotic stresses in turn allows the person skilled in the art to reduce the quantity of pesticides applied and consequently to slow down the development of resistances against the respective pesticides.
  • locus is to be understood as any type of environment, soil, area or material where the plant is growing or intended to grow as well as the environmental conditions (such as temperature, water availability, radiation) that have an influence on the growth and development of the plant and/or its propagules.
  • health of a plant or "plant health” is defined as a condition of the plant and/or its products which is determined by several aspects alone or in combination with each other such as increased yield, plant vigor, quality and tolerance to abiotic and/or biotic stress.
  • plant health indicator listed herein, and which is selected from the groups consisting of yield, plant vigor, quality and tolerance to abiotic and/or biotic stress, is to be understood as a preferred embodiment of the present invention either each on its own or in combination with each other.
  • "increased yield" of a plant, in particular of an agricultural, silvicultural and/or horticultural plant means that the yield of a product of the respective plant is increased by a measurable amount over the yield of the same product of the plant produced under the same conditions, but without the application of the compound I or the composition used according to the invention.
  • Increased yield can be characterized, among others, by the following improved properties of the plant: increased plant weight; and/or increased plant height; and/or increased biomass such as higher overall fresh weight (FW); and/or increased number of flowers per plant; and/or higher grain and/or fruit yield; and/or more tillers or side shoots (branches); and/or larger leaves;
  • chlorophyll content has a positive correlation with the plant's photosynthesis rate and accordingly, the higher the chlorophyll content the higher the yield of a plant).
  • Gram and “fruit” are to be understood as any plant product which is further utilized after harvesting, e.g. fruits in the proper sense, vegetables, nuts, grains, seeds, wood (e.g. in the case of silviculture plants), flowers (e.g. in the case of gardening plants, ornamentals) etc., that is anything of economic value that is produced by the plant.
  • the yield is preferably increased by at least 4 %, preferably at least 8 %, more preferably at least 15 %, even more preferably at least 25 %, even more preferably at least 35 %.
  • the yield is increased preferably by 5 to 10 %, more preferable by 10 to 20 %, or even 20 to 30 %. In general, the yield increase may even be higher.
  • the plant vigor becomes manifest in several aspects such as the general visual appearance.
  • Improved plant vigor can be characterized, among others, by the following improved properties of the plant: improved vitality of the plant; and/or improved plant growth; and/or improved plant development; and/or improved visual appearance; and/or improved plant stand (less plant verse/lodging); and/or improved emergence; and/or enhanced root growth and/or more developed root system; and/or enhanced nodulation, in particular rhizobial nodulation; and/or bigger leaf blade; and/or bigger size; and/or increased plant height; and/or increased tiller number; and/or increased number of side shoots; and/or increased number of flowers per plant; and/or increased shoot growth; and/or enhanced photosynthetic activity (e.g.
  • Another indicator for the condition of the plant is the "quality" of a plant and/or its products.
  • enhanced quality means that certain plant characteristics such as the content or composition of certain ingredients are increased or improved by a measurable or noticeable amount over the same factor of the plant produced under the same conditions, but without the application of the compound I or the compositions used according to the invention.
  • Enhanced quality can be characterized, among others, by following improved properties of the plant or its product: increased nutrient content; and/or increased protein content; and/or increased content of fatty acids; and/or increased metabolite content; and/or increased carotenoid content; and/or increased sugar content; and/or increased amount of essential amino acids; and/or improved nutrient composition; and/or improved protein composition; and/or improved composition of fatty acids; and/or improved metabolite composition; and/or improved carotenoid composition; and/or improved sugar composition; and/or improved amino acids composition; and/or improved or optimal fruit color; and/or improved leaf color; and/or higher storage capacity; and/or higher processability of the harvested products.
  • Biotic stress is caused by living organisms while abiotic stress is caused for example by environmental extremes.
  • "enhanced tolerance or resistance to biotic and/or abiotic stress factors” means (1 .) that certain negative factors caused by biotic and/or abiotic stress are diminished in a measurable or noticeable amount as compared to plants exposed to the same conditions, but without being treated with a compound selected from compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12, or the composition used according to the invention and (2.) that the negative effects are not diminished by a direct action of a compound selected from compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I- 7, I-8, I-9, 1-10, 1-1 1 and 1-12 on the stress factors, e.g. by its fungicidal or insecticidal action which directly destroys the microorganisms or pests, but rather by a stimulation of the plants' own defensive reactions against said stress factors.
  • Biotic stress can be caused by living organisms, such as competing plants (for example weeds), microorganisms (such as phythopathogenic fungi and/or bacteria) and/or viruses.
  • Negative factors caused by abiotic stress are also well-known and can often be observed as reduced plant vigor (see above), for example: dotted leaves, "burned leaves", reduced growth, less flowers, less biomass, less crop yields, reduced nutritional value of the crops, later crop maturity, to give just a few examples.
  • Abiotic stress can be caused for example by: extremes in temperature such as heat or cold (heat stress / cold stress); and/or strong variations in temperature; and/or temperatures unusual for the specific season; and/or drought (drought stress); and/or extreme wetness; and/or high salinity (salt stress); and/or radiation (for example by increased UV radiation due to the decreasing ozone layer); and/or increased ozone levels (ozone stress); and/or organic pollution (for example by phythotoxic amounts of pesticides); and/or inorganic pollution (for example by heavy metal contaminants).
  • extremes in temperature such as heat or cold (heat stress / cold stress); and/or strong variations in temperature; and/or temperatures unusual for the specific season; and/or drought (drought stress); and/or extreme wetness; and/or high salinity (salt stress); and/or radiation (for example by increased UV radiation due to the decreasing ozone layer); and/or increased ozone levels (ozone stress); and/or organic pollution (for example by
  • the above identified indicators for the health condition of a plant may be interdependent and may result from each other.
  • an increased resistance to biotic and/or abiotic stress may lead to a better plant vigor, e.g. to better and bigger crops, and thus to an increased yield.
  • a more developed root system may result in an increased resistance to biotic and/or abiotic stress.
  • these interdependencies and interactions are neither all known nor fully understood and therefore the different indicators are described separately.
  • a compound 1-1 is used in a method for increasing the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a compound 1-1 .
  • a compound I-2 is used in a method for increasing the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a compound I-2.
  • a compound I-3 is used in a method for increasing the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a compound I-3.
  • a compound I-4 is used in a method for increasing the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a compound I-4.
  • a compound I-5 is used in a method for increasing the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a compound I-5.
  • a compound I-6 is used in a method for increasing the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a compound I-6.
  • a compound I-7 is used in a method for increasing the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a compound I-7.
  • a compound I-8 is used in a method for increasing the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a compound 1-8.
  • a compound 1-9 is used in a method for increasing the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a compound 1-9.
  • a compound 1-10 is used in a method for increasing the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a compound 1-10.
  • a compound 1-1 1 is used in a method for increasing the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a compound 1-1 1 .
  • a compound 1-1 1 is used in a method for increasing the health of plants, wherein the plant, the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a compound 1-12.
  • the compound 1-1 is used for increasing the yield of a plant or its product.
  • compound 1-1 is used for increasing the yield such as the plant weight and/or the plant biomass (e.g. overall fresh weight) and/or the grain yield and/or the number of tillers.
  • compound I-2 is used for increasing the yield of a plant or its product.
  • compound I-2 is used for increasing the yield such as the plant weight and/or the plant biomass (e.g. overall fresh weight) and/or the grain yield and/or the number of tillers.
  • the compound I-3 is used for increasing the yield of a plant or its product.
  • compound I-3 is used for increasing the yield such as the plant weight and/or the plant biomass (e.g. overall fresh weight) and/or the grain yield and/or the number of tillers.
  • the compound I-4 is used for increasing the yield of a plant or its product.
  • compound I-4 is used for increasing the yield such as the plant weight and/or the plant biomass (e.g. overall fresh weight) and/or the grain yield and/or the number of tillers.
  • the compound I-5 is used for increasing the yield of a plant or its product. In a preferred embodiment of the invention, compound I-5 is used for increasing the yield such as the plant weight and/or the plant biomass (e.g. overall fresh weight) and/or the grain yield and/or the number of tillers. In still another embodiment the compound 1-6 is used for increasing the yield of a plant or its product. In a preferred embodiment of the invention, compound 1-6 is used for increasing the yield such as the plant weight and/or the plant biomass (e.g. overall fresh weight) and/or the grain yield and/or the number of tillers.
  • the compound 1-7 is used for increasing the yield of a plant or its product.
  • compound 1-7 is used for increasing the yield such as the plant weight and/or the plant biomass (e.g. overall fresh weight) and/or the grain yield and/or the number of tillers.
  • the compound 1-8 is used for increasing the yield of a plant or its product.
  • compound 1-8 is used for increasing the yield such as the plant weight and/or the plant biomass (e.g. overall fresh weight) and/or the grain yield and/or the number of tillers.
  • the compound 1-9 is used for increasing the yield of a plant or its product.
  • compound 1-9 is used for increasing the yield such as the plant weight and/or the plant biomass (e.g. overall fresh weight) and/or the grain yield and/or the number of tillers.
  • the compound 1-10 is used for increasing the yield of a plant or its product.
  • compound 1-10 is used for increasing the yield such as the plant weight and/or the plant biomass (e.g. overall fresh weight) and/or the grain yield and/or the number of tillers.
  • compound 1-1 1 is used for increasing the yield of a plant or its product.
  • compound 1-1 1 is used for increasing the yield such as the plant weight and/or the plant biomass (e.g. overall fresh weight) and/or the grain yield and/or the number of tillers.
  • the compound 1-12 is used for increasing the yield of a plant or its product.
  • compound 1-12 is used for increasing the yield such as the plant weight and/or the plant biomass (e.g. overall fresh weight) and/or the grain yield and/or the number of tillers.
  • the compound 1-1 is used for increasing the vigor of a plant or its product or improvement of the plant vigor.
  • the compound I-2 is used for increasing the vigor of a plant or its product or improvement of the plant vigor.
  • the compound I-3 is used for increasing the vigor of a plant or its product or improvement of the plant vigor.
  • the compound I-4 is used for increasing the vigor of a plant or its product or improvement of the plant vigor.
  • the compound I-5 is used for increasing the vigor of a plant or its product or improvement of the plant vigor.
  • the compound 1-6 is used for increasing the vigor of a plant or its product or improvement of the plant vigor.
  • the compound 1-7 is used for increasing the vigor of a plant or its product or improvement of the plant vigor.
  • the compound 1-8 is used for increasing the vigor of a plant or its product or improvement of the plant vigor.
  • the compound 1-9 is used for increasing the vigor of a plant or its product or improvement of the plant vigor.
  • the compound 1-10 is used for increasing the vigor of a plant or its product or improvement of the plant vigor.
  • the compound 1-1 1 is used for increasing the vigor of a plant or its product or improvement of the plant vigor.
  • the compound 1-12 is used for increasing the vigor of a plant or its product or improvement of the plant vigor.
  • the compound 1 is used for increasing the quality of a plant or its product.
  • the compound 2 is used for increasing the quality of a plant or its product.
  • the compound 3 is used for increasing the quality of a plant or its product.
  • the compound 4 is used for increasing the quality of a plant or its product.
  • the compound 5 is used for increasing the quality of a plant or its product.
  • the compound 6 is used for increasing the quality of a plant or its product.
  • the compound 7 is used for increasing the quality of a plant or its product.
  • the compound 8 is used for increasing the quality of a plant or its product.
  • the compound 9 is used for increasing the quality of a plant or its product.
  • the compound 10 is used for increasing the quality of a plant or its product.
  • the compound 1 1 is used for increasing the quality of a plant or its product.
  • the compound 1-12 is used for increasing the quality of a plant or its product.
  • the compound 1-1 is used for increasing the tolerance and/or resistance of a plant or its product against biotic stress.
  • the compound I-2 is used for increasing the tolerance and/or resistance of a plant or its product against biotic stress.
  • the compound I-3 is used for increasing the tolerance and/or resistance of a plant or its product against biotic stress.
  • the compound I-4 is used for increasing the tolerance and/or resistance of a plant or its product against biotic stress.
  • the compound I-5 is used for increasing the tolerance and/or resistance of a plant or its product against biotic stress.
  • the compound I-6 is used for increasing the tolerance and/or resistance of a plant or its product against biotic stress.
  • the compound I-7 is used for increasing the tolerance and/or resistance of a plant or its product against biotic stress.
  • the compound I-8 is used for increasing the tolerance and/or resistance of a plant or its product against biotic stress.
  • the compound I-9 is used for increasing the tolerance and/or resistance of a plant or its product against biotic stress.
  • the compound 1-10 is used for increasing the tolerance and/or resistance of a plant or its product against biotic stress.
  • the compound 1-1 1 is used for increasing the tolerance and/or resistance of a plant or its product against biotic stress.
  • the compound 1-12 is used for increasing the tolerance and/or resistance of a plant or its product against biotic stress.
  • the compound 1-1 is used for increasing the tolerance and/or resistance of a plant or its product against abiotic stress.
  • the compound I-2 is used for increasing the tolerance and/or resistance of a plant or its product against abiotic stress.
  • the compound I-3 is used for increasing the tolerance and/or resistance of a plant or its product against abiotic stress.
  • the compound I-4 is used for increasing the tolerance and/or resistance of a plant or its product against abiotic stress.
  • the compound I-5 is used for increasing the tolerance and/or resistance of a plant or its product against abiotic stress.
  • the compound I-6 is used for increasing the tolerance and/or resistance of a plant or its product against abiotic stress.
  • the compound I-7 is used for increasing the tolerance and/or resistance of a plant or its product against abiotic stress.
  • the compound I-8 is used for increasing the tolerance and/or resistance of a plant or its product against abiotic stress.
  • the compound I-9 is used for increasing the tolerance and/or resistance of a plant or its product against abiotic stress.
  • the compound 1-10 is used for increasing the tolerance and/or resistance of a plant or its product against abiotic stress.
  • the compound 1-1 1 is used for increasing the tolerance and/or resistance of a plant or its product against abiotic stress.
  • the compound 1-12 is used for increasing the tolerance and/or resistance of a plant or its product against abiotic stress.
  • Any one of compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12, given in the respective method or use of the invention is employed by treating the plant, plant propagation material (preferably seed), soil, area, material or environment in which a plant is growing or may grow with an effective amount of the active compounds.
  • the application can be carried out in the absense of pest pressure and/or both before and after an infection of the materials, plants or plant propagation materials (preferably seeds) by pests.
  • the active ingredient selected from compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 is used for increasing the health, specifically for improving one or more of the above mentioned particular characteristics, wherein the active ingredient selected from compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12, is applied at a growth stage (GS) between GS 00 and GS 65 BBCH of the treated plant.
  • GS growth stage
  • the active ingredient selected from compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 is used for increasing the health, specifically for improving one or more of the above mentioned particular characteristics, wherein the active ingredient selected from compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12, is applied at a growth stage (GS) between GS 00 and GS 55 BBCH of the treated plant.
  • GS growth stage
  • the active ingredient selected from compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 is used for increasing the health, specifically for improving one or more of the above mentioned particular characteristics, wherein the active ingredient selected from compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 is applied at a growth stage (GS) between GS 00 and GS 37 BBCH of the treated plant.
  • GS growth stage
  • the active ingredient selected from
  • compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 is used for increasing the health, specifically for improving one or more of the above mentioned particular characteristics, wherein the active ingredient selected from compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12, is applied at a growth stage (GS) between GS 00 and GS 21 BBCH of the treated plant.
  • GS growth stage
  • the active ingredient selected from compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 is used for increasing the health, specifically for improving one or more of the above mentioned particular characteristics, wherein the the active ingredient selected from I compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and I- 12 is applied at a growth stage (GS) between GS 13 and GS 37 BBCH of the treated plant.
  • GS growth stage
  • the term "growth stage” as used herein extended BBCH-scale which is a system for a uniform coding of phenologically similar growth stages of all mono- and dicotyledonous plant species in which the entire developmental cycle of the plants is subdivided into clearly recognizable and distinguishable longer-lasting developmental phases.
  • the BBCH-scale uses a decimal code system, which is divided into principal and secondary growth stages.
  • the abbreviation BBCH derives from the Federal Biological Research Centre for Agriculture and Forestry (Germany), the Bundessortenamt (Germany) and the chemical industry.
  • composition refers to any preparation form of the active compounds, the use of which is time- and locus-related.
  • phytopathogenic fungi comprises treating the plant propagules, preferably the seeds of an agricultural, horticultural, ornamental or silivcultural plant selected from the group consisting of transgenic or non-transgenic plants with a composition used according to the present invention.
  • plant propagation material is to be understood to denote all the generative parts of the plant such as seeds and vegetative plant material such as cuttings and tubers (e. g.
  • potatoes which can be used for the multiplication of the plant.
  • These young plants may also be protected before transplantation by a total or partial treatment by immersion or pouring.
  • treatment of plant propagation materials with the components of the inventive compositions and the inventive compositions, respectively, is used for controlling a multitude of fungi on cereals, such as wheat, rye, barley and oats; rice, corn, cotton and soybeans.
  • plants generally comprises all plants of economic importance and/or men-grown plants. They are preferably selected from agricultural, silvicultural and ornamental plants, more preferably agricultural plants and silvicultural plants, utmost preferably agricultural plants.
  • plant (or plants) is a synonym of the term “crop” which is to be understood as a plant of economic importance and/or a men-grown plant.
  • plant as used herein includes all parts of a plant such as germinating seeds, emerging seedlings, herbaceous vegetation as well as established woody plants including all belowground portions (such as the roots) and aboveground portions.
  • the plants to be treated according to the invention are selected from the group consisting of agricultural, silvicultural, ornamental and horticultural plants, each in its natural or genetically modified form, more preferably from agricultural plants. According to one embodiment, any one of compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 as defined herein is used.
  • the plant to be treated according to the method of the invention is a horticultural plant.
  • horticultural plants are to be understood as plants which are commonly used in horticulture - e.g. the cultivation of ornamentals, vegetables and/or fruits. Examples for ornamentals are turf, geranium, pelargonia, petunia, begonia and fuchsia.
  • Examples for vegetables are potatoes, tomatoes, peppers, cucurbits, cucumbers, melons, watermelons, garlic, onions, carrots, cabbage, beans, peas and lettuce and more preferably from tomatoes, onions, peas and lettuce.
  • Examples for fruits are apples, pears, cherries, strawberry, citrus, peaches, apricots and blueberries. According to one embodiment, any one of compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 as defined herein is used.
  • the plant to be treated according to the method of the invention is an ornamental plant.
  • Ornamental plants are plants which are commonly used in gardening, e.g. in parks, gardens and on balconies. Examples are turf, geranium, pelargonia, petunia, begonia and fuchsia.
  • any one of compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 as defined herein is used.
  • any one of the compositions as defined herein is used.
  • the plant to be treated according to the method of the invention is a silvicultural plant.
  • the term "silvicultural plant” is to be understood as trees, more specifically trees used in reforestation or industrial plantations.
  • Industrial plantations generally serve for the commercial production of forest products, such as wood, pulp, paper, rubber tree, Christmas trees, or young trees for gardening purposes.
  • Examples for silvicultural plants are conifers, like pines, in particular Pinus spec, fir and spruce, eucalyptus, tropical trees like teak, rubber tree, oil palm, willow (Salix), in particular Salix spec, poplar (cottonwood), in particular Populus spec, beech, in particular Fagus spec, birch, oil palm and oak.
  • any one of compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 as defined herein is used.
  • any one of the compositions as defined herein is used.
  • the plant to be treated according to the method of the invention is an agricultural plant.
  • Agricultural plants are plants of which a part or all is harvested or cultivated on a commercial scale or which serve as an important source of feed, food, fibres (e.g. cotton, linen), combustibles (e.g. wood, bioethanol, biodiesel, biomass) or other chemical compounds.
  • Agricultural plants also include the horticultural plants fruits and vegetables.
  • the term agricultural plants include cereals, e.g. wheat, rye, barley, triticale, oats, sorghum or rice; beet, e.g. sugar beet or fodder beet; fruits, such as pomes, stone fruits or soft fruits, e.g.
  • any one of compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 as defined herein is used.
  • any one of the compositions as defined herein is used.
  • the plants to be treated in accordance with the method of the present invention are agricultural plants.
  • any one of compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 as defined herein is used.
  • Preferred agricultural plants are field crops, sugar beets, cereals such as wheat, rye, barley, triticale, oats, sorghum, rice, corn, cotton, rape, sunflowers, oilseed rape, juncea and canola, vine, legumes such as soybeans, peas and beans (fieldbeans), lentil, sugar cane, turf;
  • vegetables such as vegetables, such as cucumbers, leeks, paprika spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes, cucurbits (squashes, cucumber or melons );clover and fruits, such as pomes, stone fruits or soft fruits, e.g.
  • any one of compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 as defined herein is used.
  • More preferred agricultural plants are selected from soybean, wheat, sunflower, canola, oilseed rape, corn, cotton, sugar cane, juncea, peas, lentils, alfalfa, vine, and fruits (as defined above) and vegegables as defined above).
  • Most preferred agricultural plants are selected from wheat, barley, corn, soybean, rice, canola, sunflower and fruits (as defined above) and vegetables as defined above).
  • the utmost preferred plants are soybean, vine, and fruits (as defined above) and vegetables as defined above. According to one embodiment, any one of compounds 1-1 , 1- 2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 as defined herein is used.
  • Particularly preferred agricultural plants are selected from wheat, barley soybean, corn, sugar beets, peanuts, oil seed rape, canola, rice, speciality crops, in particular specialty crops such as turf, potato, tomato, cucurbits, grapes, apples, bananas and ornamentals.
  • any one of compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 as defined herein is used.
  • compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are selected from cereals, in particular wheat and barley, and soybeans, in a specific embodiment as foliar application such as foliar spray. According to another embodiment, any one of the compositions as defined herein is used.
  • compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are selected from cereals, in particular wheat and barley, soybeans, corn, sweet corn, sorghum, sugar beet, potato, rice, sunflower, canola, pomefruit, stonefruit, legumes, dry bean and chickpea, tree nuts, peanuts, lentils, cotton, in a specific embodiment as foliar application such as foliar spray, for any one ofthe above explained plant health effects, for example cold tolerance.
  • said crops are treated by seed treatment in order to achieve the desired plant health effects.
  • any one of the compositions as defined herein is used.
  • plants also includes plants which have been modified by breeding, mutagenesis or genetic engineering (transgenic and non-transgenic plants).
  • Genetically modified plants are plants, which genetic material has been modified by the use of recombinant DNA techniques in a way that it cannot readily be obtained by cross breeding under natural circumstances, mutations or natural recombination.
  • any one of compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 as defined herein is used.
  • any one of the compositions as defined herein is used.
  • Plants as well as the propagation material of said plants which can be treated with a compound selected from compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12, or the composition used according to the invention, include all modified non-transgenic plants or transgenic plants, e.g. crops which tolerate the action of herbicides or fungicides or insecticides owing to breeding, including genetic engineering methods, or plants which have modified characteristics in comparison with existing plants, which can be generated for example by traditional breeding methods and/or the generation of mutants, or by recombinant procedures.
  • any one of compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 as defined herein is used.
  • any one of the compositions as defined herein is used.
  • a compound selected from compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, I- 1 1 and 1-12 as defined herein, or compositions according to the present invention or used according to the present invention can be applied (as seed treatment, foliar spray treatment, in- furrow application or by any other means) also to plants which have been modified by breeding, mutagenesis or genetic engineering including but not limiting to agricultural biotech products on the market or in development (cf. http://www.bio.org/speeches/pubs/er/agri_products.asp).
  • Genetically modified plants are plants, which genetic material has been so modified by the use of recombinant DNA techniques that under natural circumstances cannot readily be obtained by cross breeding, mutations or natural recombination.
  • one or more genes have been integrated into the genetic material of a genetically modified plant in order to improve certain properties of the plant.
  • Such genetic modifications also include but are not limited to targeted post-transitional modification of protein(s), oligo- or polypeptides e.g. by glycosylation or polymer additions such as prenylated, acetylated or farnesylated moieties or PEG moieties.
  • Tolerance to herbicides can be obtained by creating insensitivity at the site of action of the herbicide by expression of a target enzyme which is resistant to herbicide; rapid metabolism (conjugation or degradation) of the herbicide by expression of enzymes which inactivate herbicide; or poor uptake and translocation of the herbicide.
  • Examples are the expression of enzymes which are tolerant to the herbicide in comparison to wild type enzymes, such as the expression of 5- enolpyruvylshikimate-3-phosphate synthase (EPSPS), which is tolerant to glyphosate (see e.g. Heck et.al, Crop Sci.
  • EPSPS 5- enolpyruvylshikimate-3-phosphate synthase
  • Zea mays with chimeric gene sequences coging for HDDP see e.g. W01996/38567, WO 2004/55191 ); Arabidopsis thaliana which is resistant to protox inhibitors (see e.g. US2002/0073443).
  • Rootworm/RR2® and "YieldGard VT Triple®” (Monsanto) with tolerance to glyphosate
  • corn varieties “Liberty Link®” Bayer
  • Herculex I® "Herculex RW®”
  • Herculex® Xtra (Dow, Pioneer)
  • Agrisure GT/CB/LL® and “Agrisure CB/LL/RW®” (Syngenta) with tolerance to glufosinate
  • cotton variety "FiberMax Liberty Link®” (Bayer) with tolerance to glufosinate
  • the cotton variety "BXN®” (Calgene) with tolerance to bromoxynil
  • toxins produced by animals such as scorpion toxins, arachnid toxins, wasp toxins, or other insect-specific neurotoxins
  • toxins produced by fungi such Streptomycetes toxins, plant lectins, such as pea or barley lectins; agglutinins
  • proteinase inhibitors such as trypsin inhibitors, serine protease inhibitors, patatin, cystatin or papain inhibitors
  • ribosome-inactivating proteins (RIP) such as ricin, maize-RIP, abrin, luffin, saporin or bryodin
  • steroid metabolism enzymes such as 3- hydroxysteroid oxidase, ecdysteroid-IDP-glycosyl-transferase, cholesterol oxidases, ecdysone inhibitors or HMG-CoA-reductase
  • ion channel blockers such as blockers of sodium or calcium
  • these insecticidal proteins or toxins are to be understood expressly also as pre-toxins, hybrid proteins, truncated or otherwise modified proteins.
  • Hybrid proteins are characterized by a new combination of protein domains, (see, e. g. WO 02/015701 ).
  • Further examples of such toxins or genetically modified plants capable of synthesizing such toxins are disclosed, e.g., in EP- A 374 753, WO 93/007278, WO 95/34656, EP-A 427 529, EP-A 451 878, WO 03/18810 und WO 03/52073.
  • the methods for producing such genetically modified plants are generally known to the person skilled in the art and are described, e. g.
  • insecticidal proteins contained in the genetically modified plants impart to the plants producing these proteins tolerance to harmful pests from all taxonomic groups of athropods, especially to beetles (Coeloptera), two-winged insects (Diptera), and moths (Lepidoptera) and to nematodes (Nematoda).
  • WO 03/018810 MON 863 from Monsanto Europe S.A., Belgium (corn cultivars producing the Cry3Bb1 toxin), IPC 531 from Monsanto Europe S.A., Belgium (cotton cultivars producing a modified version of the CrylAc toxin) and 1507 from Pioneer Overseas Corporation, Belgium (corn cultivars producing the Cry1 F toxin and PAT enzyme).
  • plants are also covered that are by the use of recombinant DNA techniques capable to synthesize one or more proteins to increase the resistance or tolerance of those plants to bacterial, viral or fungal pathogens.
  • proteins are the so-called "pathogenesis-related proteins" (PR proteins, see, e.g. EP-A 392225), plant disease resistance genes (e. g. potatoecultivars, which express resistance genes acting against Phytophthora infestans derived from the mexican wild potatoeSolanum bulbocastanum) or T4-lysozym (e.g. potatoecultivars capable of synthesizing these proteins with increased resistance against bacteria such as Erwinia amylvora).
  • PR proteins pathogenesis-related proteins
  • plant disease resistance genes e. g. potatoecultivars, which express resistance genes acting against Phytophthora infestans derived from the mexican wild potatoeSolanum bulbocastanum
  • T4-lysozym e.
  • plants are also covered that are by the use of recombinant DNA techniques capable to synthesize one or more proteins to increase the productivity (e.g. bio mass production, grain yield, starch content, oil content or protein content), tolerance to drought, salinity or other growth-limiting environmental factors or tolerance to pests and fungal, bacterial or viral pathogens of those plants.
  • productivity e.g. bio mass production, grain yield, starch content, oil content or protein content
  • plants are also covered that contain by the use of recombinant DNA techniques a modified amount of substances of content or new substances of content, specifically to improve human or animal nutrition, e.g. oil crops that produce health-promoting long-chain omega-3 fatty acids or unsaturated omega-9 fatty acids (e.g. Nexera® rape, DOW Agro Sciences, Canada).
  • a modified amount of substances of content or new substances of content specifically to improve human or animal nutrition, e.g. oil crops that produce health-promoting long-chain omega-3 fatty acids or unsaturated omega-9 fatty acids (e.g. Nexera® rape, DOW Agro Sciences, Canada).
  • plants are also covered that contain by the use of recombinant DNA techniques a modified amount of substances of content or new substances of content, specifically to improve raw material production, e.g. potatoes that produce increased amounts of amylopectin (e.g. Amflora® potato, BASF SE, Germany).
  • a modified amount of substances of content or new substances of content specifically to improve raw material production, e.g. potatoes that produce increased amounts of amylopectin (e.g. Amflora® potato, BASF SE, Germany).
  • plant propagation material is to be understood to denote all the generative parts of the plant such as seeds and vegetative plant material such as cuttings and tubers (e.g.
  • potatoes which can be used for the multiplication of the plant.
  • This includes seeds, grains, roots, fruits, tubers, bulbs, rhizomes, cuttings, spores, offshoots, shoots, sprouts and other parts of plants, including seedlings and young plants, which are to be transplanted after germination or after emergence from soil, meristem tissues, single and multiple plant cells and any other plant tissue from which a complete plant can be obtained.
  • propagules or "plant propagules” is to be understood to denote any structure with the capacity to give rise to a new plant, e.g. a seed, a spore, or a part of the vegetative body capable of independent growth if detached from the parent.
  • the term “propagules” or “plant propagules” denotes for seed.
  • the health of a plant is increased.
  • the application rates of the compounds selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 or the compositions used according to the invention are from 0,5 g/ha to 2000 g/ha, preferably 1 g/ha to 1000 g/ha, more preferably from 5 to 500g/ha, in particular from 25 to 250 g/ha.
  • the application rates of the compound selected from -1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are in particular between 5 g/ha and 500 g/ha, depending on various parameters such as the treated plant species or the composition applied.
  • the application rates of the compound selected from -1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I- 9, 1-10, 1-1 1 and 1-12 are between 5 g/ha and 500 g/ha.
  • the application rates of the compound selected from I- 1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are between 5 g/ha and 500 g/ha, in particular from 25 g/ha to 250 g/ha.
  • amounts of from 0,01 g to 3 kg in particular amounts from 0,01 g to 1 kg of the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are generally required per 100 kg of plant propagation material (preferably seed).
  • amounts of from 0,01 g to 250 g of the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are required per 100 kg of plant propagation material (preferably seed).
  • amounts of from 0,01 g to 150 g of the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are required per 100 kg of plant.
  • the application rates are in the range of from 0,1 to 6,0 kg of active ingredient (acid equivalent) per hectare, depending on various parameters such as the weather conditions and the plant species.
  • the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are used in "effective amounts". This means that they are used in a quantity which allows obtaining the desired effect which is a synergistic increase of the health of a plant but which does not give rise to any phytotoxic symptom on the treated plant. All compounds selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are typically applied as compositions comprising component I.
  • the pesticial composition comprises a liquid or solid carrier and a mixture as described above.
  • the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 can be converted into the customary formulations, for example solutions, emulsions, suspensions, dusts, powders, pastes and granules.
  • the use form depends on the particular intended purpose; in each case, it should ensure a fine and even distribution of the compositions usedaccording to the present invention.
  • the formulations are prepared in a known manner (cf. US 3,060,084, EP-A 707 445 (for liquid concentrates), Browning: "Agglomeration", Chemical Engineering, Dec.
  • the agrochemical formulations may also comprise auxiliaries which are customary in agrochemical formulations.
  • the auxiliaries used depend on the particular application form and active substance, respectively.
  • suitable auxiliaries are solvents, solid carriers, dispersants or emulsifiers (such as further solubilizers, protective colloids, surfactants and adhesion agents), organic and inorganic thickeners, bactericides, anti-freezing agents, anti- foaming agents, if appropriate colorants and tackifiers or binders (e.g. for seed treatment formulations).
  • Suitable solvents are water, organic solvents such as mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g.
  • Solid carriers are mineral earths such as silicates, silica gels, talc, kaolins, limestone, lime, chalk, bole, loess, clays, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.
  • mineral earths such as silicates, silica gels, talc, kaolins, limestone, lime, chalk, bole, loess, clays, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, e.g. ammonium sulfate, ammonium phosphate, ammoni
  • Suitable surfactants are alkali metal, alkaline earth metal and ammonium salts of aromatic sulfonic acids, such as ligninsoulfonic acid (Borresperse® types, Borregard, Norway) phenolsulfonic acid, naphthalenesulfonic acid (Morwet® types, Akzo Nobel, U.S.A.), dibutylnaphthalene-sulfonic acid (Nekal® types, BASF, Germany), and fatty acids, alkylsulfonates, alkylarylsulfonates, alkyl sulfates, laurylether sulfates, fatty alcohol sulfates, and sulfated hexa-, hepta- and octadecanolates, sulfated fatty alcohol glycol ethers, furthermore condensates of aromatic sulfonic acids, such as ligninsoulfonic acid (Borresperse® types
  • polyoxypropylene lauryl alcohol polyglycol ether acetal, sorbitol esters, lignin-sulfite waste liquid and proteins, denatured proteins, polysaccharides (e.g. methylcellulose), hydrophobically modified starches, polyvinyl alcohols (Mowiol® types, Clariant, Switzerland), polycarboxylates (Sokolan® types, BASF, Germany), polyalkoxylates, polyvinylamines (Lupasol® types, BASF, Germany), polyvinylpyrrolidone and the copolymers therof.
  • thickeners i.e.
  • polysaccharides and organic and inorganic clays such as Xanthan gum (Kelzan®, CP Kelco, U.S.A.), Rhodopol® 23 (Rhodia, France), Veegum® (R.T. Vanderbilt, U.S.A.) or Attaclay® (Engelhard Corp., NJ, USA).
  • Bactericides may be added for preservation and stabilization of the formulation.
  • suitable bactericides are those based on dichlorophene and benzylalcohol hemi formal (Proxel® from ICI or Acticide® RS from Thor Chemie and Kathon® MK from Rohm & Haas) and isothiazolinone derivatives such as alkylisothiazolinones and benzisothiazolinones (Acticide® MBS from Thor Chemie).
  • suitable anti-freezing agents are ethylene glycol, propylene glycol, urea and glycerin.
  • anti-foaming agents are silicone emulsions (such as e.g. Silikon® SRE, Wacker, Germany or Rhodorsil®, Rhodia, France), long chain alcohols, fatty acids, salts of fatty acids, fluoroorganic compounds and mixtures thereof.
  • Suitable colorants are pigments of low water solubility and water-soluble dyes. Examples to be mentioned und the designations rhodamin B, C. I. pigment red 1 12, C. I. solvent red 1 , pigment blue 15:4, pigment blue 15:3, pigment blue 15:2, pigment blue 15:1 , pigment blue 80, pigment yellow 1 , pigment yellow 13, pigment red 1 12, pigment red 48:2, pigment red 48:1 , pigment red 57:1 , pigment red 53:1 , pigment orange 43, pigment orange 34, pigment orange 5, pigment green 36, pigment green 7, pigment white 6, pigment brown 25, basic violet 10, basic violet 49, acid red 51 , acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108.
  • tackifiers or binders examples include polyvinylpyrrolidons, polyvinylacetates, polyvinyl alcohols and cellulose ethers (Tylose®, Shin-Etsu, Japan).
  • Powders, materials for spreading and dusts can be prepared by mixing or concomitantly grinding compound I, if appropriate, further active substances, with at least one solid carrier.
  • Granules e.g. coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active substances to solid carriers.
  • solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, e.g., ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.
  • formulation types are:
  • Emulsions (EW, EO, ES)
  • 25 parts by weight of compounds of the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight).
  • This mixture is introduced into 30 parts by weight of water by means of an emulsifying machine (Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion.
  • the composition has an active substance content of 25% by weight.
  • 50 parts by weight of compounds of the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are ground finely with addition of 50 parts by weight of dispersants and wetting agents and prepared as water-dispersible or water-soluble granules by means of technical appliances (e. g. extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active substance.
  • the composition has an active substance content of 50% by weight.
  • 75 parts by weight of compounds of the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are ground in a rotor-stator mill with addition of 25 parts by weight of dispersants, wetting agents and silica gel. Dilution with water gives a stable dispersion or solution of the active substance.
  • the active substance content of the composition is 75% by weight.
  • Dustable powders (DP, DS)
  • the agrochemical formulations generally comprise between 0.01 and 95%, preferably between 0.1 and 90%, most preferably between 0.5 and 90%, by weight of active substances.
  • the compound selected from 1-1 , I-2, I-3, I-4 and I-5 or the compounds of the compositions used according to the invention are employed in a purity of from 90% to 100%, preferably from 95% to 100% (according to NMR spectrum).
  • the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 can be used as such or in the form of their compositions, e.g. in the form of directly sprayable solutions, powders, suspensions, dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading, brushing, immersing or pouring.
  • the application forms depend entirely on the intended purposes; it is intended to ensure in each case the finest possible distribution of the compounds present in the compositions used according to the invention.
  • Aqueous application forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water.
  • emulsions, pastes or oil dispersions the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier.
  • concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil and such concentrates are suitable for dilution with water.
  • the active substance concentrations in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.001 to 1 % by weight of the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12.
  • the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply compositions comprising over 95% by weight of active substance, or even to apply the active substance without additives.
  • UUV ultra-low-volume process
  • oils, wetters, adjuvants, herbicides, fungicides, other pesticides, or bactericides may be added to the active compounds, if appropriate not until immediately prior to use (tank mix).
  • These agents can be admixed with the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I- 7, I-8, I-9, 1-10, 1-1 1 and 1-12 in a weight ratio of 1 :100 to 100:1 , preferably 1 :10 to 10:1 .
  • compositions of this invention may also contain fertilizers such as ammonium nitrate, urea, potash, and superphosphate, phytotoxicants and plant growth regulators and safeners. These may be used sequentially or in combination with the above-described compositions, if appropriate also added only immediately prior to use (tank mix). For example, the plant(s) may be sprayed with a composition of this invention or composition used according to the invention either before or after being treated with the fertilizers.
  • fertilizers such as ammonium nitrate, urea, potash, and superphosphate, phytotoxicants and plant growth regulators and safeners.
  • compositions as defined above can be applied simultaneously, that is jointly or separately, or in succession, the sequence, in the case of separate application, generally not having any effect on the result of the control measures.
  • a variant of the present invention also comprises seed treatment with component II followed by foliar spraying with component I.
  • Seed treatment can be made into the seedbox before planting into the field.
  • the weight ratio in the compositions generally depends on the properties of the compounds of the compositions.
  • compositions which are especially useful for seed treatment are e.g.:
  • a Soluble concentrates (SL, LS)
  • compositions can be applied to plant propagation materials, particularly seeds, diluted or undiluted.
  • the compositions in question give, after two-to-tenfold dilution, active substance concentrations of from 0.01 to 60% by weight, preferably from 0.1 to 40% by weight, in the ready-to-use preparations. Application can be carried out before or during sowing.
  • Methods for applying or treating agrochemical compounds and compositions thereof, respectively, on to plant propagation material, especially seeds are known in the art, and include dressing, coating, pelleting, dusting and soaking application methods of the propagation material (and also in furrow treatment).
  • the compounds or the compositions thereof, respectively are applied on to the plant propagation material by a method such that germination is not induced, e. g. by seed dressing, pelleting, coating and dusting.
  • the application rates of the compound selected from 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, 1-10, 1-1 1 and 1-12 are generally for the formulated product (which usually comprises from 10 to 750 g/l of the active(s)). Further suitable application rates see above.
  • the invention also relates to the use of propagation products of plants, and especially the seed comprising, that is, coated with and/or containing, a composition containing of two or more active ingredients or a mixture of two or more compositions each providing one of the active ingredients.
  • the plant propagation material (preferably seed) comprises the compositions used according to the invention in an amount of from 0.01 g to 10 kg per 100 kg of plant propagation material (preferably seed).
  • the separate or joint application of the compound I of the compositions used according to the invention is carried out by spraying or dusting the seeds, the seedlings, the plants or the soils before or after sowing of the plants or before or after emergence of the plants.
  • all agrochemical formulations as described above may comprise further active ingredients, i.e. fungicides, insecticides, microbials, herbicides and/or plant growth regulator.
  • compositions comprising any of the compounds 1-1 , I-2, I-3, I-4, I-5, I-6, I-7, I-8, I-9, I- 10, 1-1 1 and 1-12 and one further active ingredient
  • health of a plant may be increased synergistically.
  • the term "synergistically” refers to the fact that the purely additive effect (in mathematical terms) of a simultaneous, that is joint or separate application of one compound I and a further active ingredient, or the successive application of one compound I and a further active ingredient, of the application of the individual compound I.

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
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  • General Health & Medical Sciences (AREA)
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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

La présente invention concerne un procédé qui permet d'améliorer la santé d'une plante, la plante, l'endroit où la plante pousse ou s'apprête à pousser ou un matériel de propagation de plante, à partir duquel la plante pousse, étant traité avec une quantité efficace d'un principe actif, choisi parmi le groupe constitué de 1-[3-chloro-2-[[1-(4-chlorophényl)pyrazol-3-yl]oxyméthyl]phényl]-4- méthyl-tétrazol-5-one (I-1), 1-[3-bromo-2-[[1-(4-chlorophényl)pyrazol-3-yl]oxyméthyl]phényl]-4- méthyl-tétrazol-5-one (I-2), 1-[2-[[1-(4-chlorophényl)pyrazol-3-yl]oxyméthyl]-3-méthyl-phényl]-4- méthyl-tétrazol-5-one (I-3), 1-[2-[[1-(4-chlorophényl)pyrazol-3-yl]oxyméthyl]-3-fluoro-phényl]-4- méthyl-tétrazol-5-one (I-4), 1-[2-[[1-(2,4-dichlorophényl)pyrazol-3-yl]oxyméthyl]-3-fluoro-phényl]- 4-méthyl-tétrazol-5-one (I-5), 1-[2-[[4-(4-chlorophényl)thiazol-2-yl]oxyméthyl]-3-méthyl-phényl]- 4-méthyl-tétrazol-5-one (I-6), 1-[3-chloro-2-[[4-(p-tolyl)thiazol-2-yl]oxyméthyl]phényl]-4-méthyl- tétrazol-5-one (I-7), 1-[3-cyclopropyl-2-[[2-méthyl-4-(1-méthylpyrazol-3- yl)phénoxy]méthyl]phényl]-4-méthyl-tétrazol-5-one (I-8), 1-[3-(difluorométhoxy)-2-[[2-méthyl-4- (1-méthylpyrazol-3-yl)phénoxy]méthyl]phényl]-4-méthyl-tétrazol-5-one (I-9), 1-méthyl-4-[3- méthyl-2-[[2-méthyl-4-(1-méthylpyrazol-3-yl)phénoxy]méthyl]phényl]tétrazol-5-one (I-10) et 1- méthyl-4-[3-méthyl-2-[[1-[3-(trifluorométhyl)phényl]éthylideneamino]oxyméthyl]phényl]tétrazol-5- one (I-11) et 1-[3-chloro-2-[[1-(4-chlorophényl)pyrazol-3-yl]oxyméthyl]phényl]-4-méthyl- tétrazol-5-one (I-12).
PCT/EP2015/078334 2014-12-12 2015-12-02 Procédé d'amélioration de la santé de plante WO2016091675A1 (fr)

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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018050508A1 (fr) * 2016-09-13 2018-03-22 Basf Se Mélanges pesticides
EP3338552A1 (fr) * 2016-12-21 2018-06-27 Basf Se Utilisation d'un fongicide tetrazolinone sur des plantes transgéniques
WO2019052898A1 (fr) * 2017-09-13 2019-03-21 Basf Se Nouvelles formulations agrochimiques
EP3616515A1 (fr) * 2018-08-31 2020-03-04 Sumitomo Chemical Company, Limited Composition et procédé de lutte contre les maladies des plantes
EP3616517A1 (fr) * 2018-08-31 2020-03-04 Sumitomo Chemical Company, Limited Composition et procédé de lutte contre les maladies des plantes
EP3616516A1 (fr) * 2018-08-31 2020-03-04 Sumitomo Chemical Company, Limited Composition de lutte de maladies végétales et procédé de lutte de maladies végétales
US10779536B2 (en) 2014-11-07 2020-09-22 Basf Se Pesticidal mixtures
US10905122B2 (en) 2016-03-16 2021-02-02 Basf Se Use of tetrazolinones for combating resistant phytopathogenic fungi on cereals
US10959431B2 (en) 2016-10-10 2021-03-30 Basf Se Pesticidal mixtures
US11241012B2 (en) 2016-03-16 2022-02-08 Basf Se Use of tetrazolinones for combating resistant phytopathogenic fungi on soybean
US11425909B2 (en) 2016-03-16 2022-08-30 Basf Se Use of tetrazolinones for combating resistant phytopathogenic fungi on fruits
US12302901B2 (en) 2014-11-07 2025-05-20 Basf Se Pesticidal mixtures

Citations (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3060084A (en) 1961-06-09 1962-10-23 Du Pont Improved homogeneous, readily dispersed, pesticidal concentrate
US3299566A (en) 1964-06-01 1967-01-24 Olin Mathieson Water soluble film containing agricultural chemicals
US3920442A (en) 1972-09-18 1975-11-18 Du Pont Water-dispersible pesticide aggregates
US4144050A (en) 1969-02-05 1979-03-13 Hoechst Aktiengesellschaft Micro granules for pesticides and process for their manufacture
US4172714A (en) 1976-12-20 1979-10-30 E. I. Du Pont De Nemours And Company Dry compactible, swellable herbicidal compositions and pellets produced therefrom
GB2095558A (en) 1981-03-30 1982-10-06 Avon Packers Ltd Formulation of agricultural chemicals
US4761373A (en) 1984-03-06 1988-08-02 Molecular Genetics, Inc. Herbicide resistance in plants
EP0374753A2 (fr) 1988-12-19 1990-06-27 American Cyanamid Company Toxines insecticides, gènes les codant, anticorps les liant, ainsi que cellules végétales et plantes transgéniques exprimant ces toxines
US4940835A (en) 1985-10-29 1990-07-10 Monsanto Company Glyphosate-resistant plants
EP0392225A2 (fr) 1989-03-24 1990-10-17 Ciba-Geigy Ag Plantes transgéniques résistantes aux maladies
US5013659A (en) 1987-07-27 1991-05-07 E. I. Du Pont De Nemours And Company Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
EP0427529A1 (fr) 1989-11-07 1991-05-15 Pioneer Hi-Bred International, Inc. Lectines larvicides, et résistance induite des plantes aux insectes
WO1991013546A1 (fr) 1990-03-12 1991-09-19 E.I. Du Pont De Nemours And Company Granules pesticides dispersibles ou solubles dans l'eau, obtenus a partir de liants thermo-actives
EP0451878A1 (fr) 1985-01-18 1991-10-16 Plant Genetic Systems, N.V. Modification de plantes par techniques de génie génétique pour combattre ou contrôler les insectes
US5180587A (en) 1988-06-28 1993-01-19 E. I. Du Pont De Nemours And Company Tablet formulations of pesticides
US5188642A (en) 1985-08-07 1993-02-23 Monsanto Company Glyphosate-resistant plants
WO1993007278A1 (fr) 1991-10-04 1993-04-15 Ciba-Geigy Ag Sequence d'adn synthetique ayant une action insecticide accrue dans le mais
US5208030A (en) 1989-08-30 1993-05-04 Imperial Chemical Industries Plc Active ingredient dosage device
US5232701A (en) 1990-10-11 1993-08-03 Sumitomo Chemical Company, Limited Boron carbonate and solid acid pesticidal composition
US5304732A (en) 1984-03-06 1994-04-19 Mgi Pharma, Inc. Herbicide resistance in plants
WO1995034656A1 (fr) 1994-06-10 1995-12-21 Ciba-Geigy Ag Nouveaux genes du bacillus thuringiensis codant pour des toxines actives contre les lepidopteres
EP0707445A1 (fr) 1993-07-03 1996-04-24 Basf Ag Formulation aqueuse polyphasee et stable prete a l'emploi pour produits phytosanitaires et procede de preparation
US5561236A (en) 1986-03-11 1996-10-01 Plant Genetic Systems Genetically engineered plant cells and plants exhibiting resistance to glutamine synthetase inhibitors, DNA fragments and recombinants for use in the production of said cells and plants
WO1996038567A2 (fr) 1995-06-02 1996-12-05 Rhone-Poulenc Agrochimie Sequence adn d'un gene de l'hydroxy-phenyl pyruvate dioxygenase et obtention de plantes contenant un gene de l'hydroxy-phenyl pyruvate dioxygenase, tolerantes a certains herbicides
US5608147A (en) 1994-01-11 1997-03-04 Kaphammer; Bryan J. tfdA gene selectable markers in plants and the use thereof
US5627061A (en) 1990-08-31 1997-05-06 Monsanto Company Glyphosate-tolerant 5-enolpyruvylshikimate-3-phosphate synthases
US5670454A (en) 1994-12-15 1997-09-23 Basf Aktiengesellschaft Herbicides of the auxin type for treating transgenic crop plants
WO1997049816A1 (fr) 1996-06-27 1997-12-31 E.I. Du Pont De Nemours And Company Gene de plantes de la p-hydroxyphenylpyruvate dioxygenase
US6100446A (en) 1986-08-29 2000-08-08 Hoechst Schering Agrevo Gmbh Microorganisms and plasmids for 2,4-dichlorophenoxyacetic acid (2,4-D)monooxygenase formation and process for the production of these plasmids and strains
US6211439B1 (en) 1984-08-10 2001-04-03 Mgi Pharma, Inc Herbicide resistance in plants
WO2002015701A2 (fr) 2000-08-25 2002-02-28 Syngenta Participations Ag Nouvelles toxines insecticides derivees de proteines cristallines insecticides de $i(bacillus thuringiensis)
US20020073443A1 (en) 1996-02-28 2002-06-13 Heifetz Peter B. Herbicide tolerance achieved through plastid transformation
WO2003018810A2 (fr) 2001-08-31 2003-03-06 Syngenta Participations Ag Toxines cry3a modifiees et sequences d'acides nucleiques les codant
WO2003052073A2 (fr) 2001-12-17 2003-06-26 Syngenta Participations Ag Nouvel evenement du mais
WO2004055191A1 (fr) 2002-12-17 2004-07-01 Biogemma Expression de la dioxygenase du pyruvate d'hydroxyphenyle dans les plastes de plantes pour la tolerance aux herbicides
US6791014B2 (en) 2000-08-11 2004-09-14 Aventis Cropscience, S.A. Use of HPPD inhibitors as selection agents in plant transformation
WO2005107437A2 (fr) 2004-04-30 2005-11-17 Dow Agrosciences Llc Nouveaux genes de resistance aux herbicides
WO2006060634A2 (fr) 2004-12-01 2006-06-08 Basf Agrochemical Products, B.V. Nouvelle mutation impliquee dans l'accroissement de la resistance aux herbicides d'imidazolinone dans les plantes
US7105724B2 (en) 1997-04-04 2006-09-12 Board Of Regents Of University Of Nebraska Methods and materials for making and using transgenic dicamba-degrading organisms
US20080052798A1 (en) 2006-03-09 2008-02-28 E.I. Du Pont De Nemours And Company Polynucleotide Encoding a Maize Herbicide Resistance Gene and Methods for Use
WO2008051633A2 (fr) 2006-10-25 2008-05-02 Monsanto Technology Llc Systèmes de culture destinés à lutter contre les mauvaises herbes
US20090105077A1 (en) 2006-10-16 2009-04-23 Monsanto Technology Llc Methods and compositions for improving plant health
WO2013162077A1 (fr) 2012-04-27 2013-10-31 Sumitomo Chemical Company, Limited Composés de tétrazolinone et leur utilisation
WO2013162072A1 (fr) 2012-04-27 2013-10-31 Sumitomo Chemical Company, Limited Composés de tétrazolinone et leur utilisation en tant que pesticides
WO2014051165A1 (fr) 2012-09-28 2014-04-03 Sumitomo Chemical Company, Limited Composés de tétrazolinone et leur utilisation comme pesticides
WO2014051161A1 (fr) 2012-09-28 2014-04-03 Sumitomo Chemical Company, Limited Composés tétrazolinone et leur utilisation en tant que pesticide
WO2014084223A1 (fr) 2012-11-29 2014-06-05 住友化学株式会社 Composé de tétrazolinone et son utilisation

Patent Citations (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3060084A (en) 1961-06-09 1962-10-23 Du Pont Improved homogeneous, readily dispersed, pesticidal concentrate
US3299566A (en) 1964-06-01 1967-01-24 Olin Mathieson Water soluble film containing agricultural chemicals
US4144050A (en) 1969-02-05 1979-03-13 Hoechst Aktiengesellschaft Micro granules for pesticides and process for their manufacture
US3920442A (en) 1972-09-18 1975-11-18 Du Pont Water-dispersible pesticide aggregates
US4172714A (en) 1976-12-20 1979-10-30 E. I. Du Pont De Nemours And Company Dry compactible, swellable herbicidal compositions and pellets produced therefrom
GB2095558A (en) 1981-03-30 1982-10-06 Avon Packers Ltd Formulation of agricultural chemicals
US6222100B1 (en) 1984-03-06 2001-04-24 Mgi Pharma, Inc. Herbicide resistance in plants
US4761373A (en) 1984-03-06 1988-08-02 Molecular Genetics, Inc. Herbicide resistance in plants
US6211438B1 (en) 1984-03-06 2001-04-03 Mgi Pharma, Inc. Herbicide resistance in plants
US5304732A (en) 1984-03-06 1994-04-19 Mgi Pharma, Inc. Herbicide resistance in plants
US6211439B1 (en) 1984-08-10 2001-04-03 Mgi Pharma, Inc Herbicide resistance in plants
EP0451878A1 (fr) 1985-01-18 1991-10-16 Plant Genetic Systems, N.V. Modification de plantes par techniques de génie génétique pour combattre ou contrôler les insectes
US5188642A (en) 1985-08-07 1993-02-23 Monsanto Company Glyphosate-resistant plants
US4940835A (en) 1985-10-29 1990-07-10 Monsanto Company Glyphosate-resistant plants
US5646024A (en) 1986-03-11 1997-07-08 Plant Genetic Systems, N.V. Genetically engineered plant cells and plants exhibiting resistance to glutamine synthetase inhibitors, DNA fragments and recombinants for use in the production of said cells and plants
US5561236A (en) 1986-03-11 1996-10-01 Plant Genetic Systems Genetically engineered plant cells and plants exhibiting resistance to glutamine synthetase inhibitors, DNA fragments and recombinants for use in the production of said cells and plants
US6153401A (en) 1986-08-29 2000-11-28 Hoechst Schering Agrevo Gnbh Microorganisms and plasmids for 2,4-dichlorophenoxyacetic acid (2,4-D) monooxygenase formation and process for the production of these plasmids and strains
US6100446A (en) 1986-08-29 2000-08-08 Hoechst Schering Agrevo Gmbh Microorganisms and plasmids for 2,4-dichlorophenoxyacetic acid (2,4-D)monooxygenase formation and process for the production of these plasmids and strains
US5013659A (en) 1987-07-27 1991-05-07 E. I. Du Pont De Nemours And Company Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
US5180587A (en) 1988-06-28 1993-01-19 E. I. Du Pont De Nemours And Company Tablet formulations of pesticides
EP0374753A2 (fr) 1988-12-19 1990-06-27 American Cyanamid Company Toxines insecticides, gènes les codant, anticorps les liant, ainsi que cellules végétales et plantes transgéniques exprimant ces toxines
EP0392225A2 (fr) 1989-03-24 1990-10-17 Ciba-Geigy Ag Plantes transgéniques résistantes aux maladies
US5208030A (en) 1989-08-30 1993-05-04 Imperial Chemical Industries Plc Active ingredient dosage device
EP0427529A1 (fr) 1989-11-07 1991-05-15 Pioneer Hi-Bred International, Inc. Lectines larvicides, et résistance induite des plantes aux insectes
WO1991013546A1 (fr) 1990-03-12 1991-09-19 E.I. Du Pont De Nemours And Company Granules pesticides dispersibles ou solubles dans l'eau, obtenus a partir de liants thermo-actives
US5627061A (en) 1990-08-31 1997-05-06 Monsanto Company Glyphosate-tolerant 5-enolpyruvylshikimate-3-phosphate synthases
US5804425A (en) 1990-08-31 1998-09-08 Monsanto Company Glyphosate-tolerant 5-enolpyruvylshikimate-3-phosphate synthases
US5633435A (en) 1990-08-31 1997-05-27 Monsanto Company Glyphosate-tolerant 5-enolpyruvylshikimate-3-phosphate synthases
US5232701A (en) 1990-10-11 1993-08-03 Sumitomo Chemical Company, Limited Boron carbonate and solid acid pesticidal composition
WO1993007278A1 (fr) 1991-10-04 1993-04-15 Ciba-Geigy Ag Sequence d'adn synthetique ayant une action insecticide accrue dans le mais
EP0707445A1 (fr) 1993-07-03 1996-04-24 Basf Ag Formulation aqueuse polyphasee et stable prete a l'emploi pour produits phytosanitaires et procede de preparation
US5608147A (en) 1994-01-11 1997-03-04 Kaphammer; Bryan J. tfdA gene selectable markers in plants and the use thereof
WO1995034656A1 (fr) 1994-06-10 1995-12-21 Ciba-Geigy Ag Nouveaux genes du bacillus thuringiensis codant pour des toxines actives contre les lepidopteres
US5670454A (en) 1994-12-15 1997-09-23 Basf Aktiengesellschaft Herbicides of the auxin type for treating transgenic crop plants
WO1996038567A2 (fr) 1995-06-02 1996-12-05 Rhone-Poulenc Agrochimie Sequence adn d'un gene de l'hydroxy-phenyl pyruvate dioxygenase et obtention de plantes contenant un gene de l'hydroxy-phenyl pyruvate dioxygenase, tolerantes a certains herbicides
US20020073443A1 (en) 1996-02-28 2002-06-13 Heifetz Peter B. Herbicide tolerance achieved through plastid transformation
WO1997049816A1 (fr) 1996-06-27 1997-12-31 E.I. Du Pont De Nemours And Company Gene de plantes de la p-hydroxyphenylpyruvate dioxygenase
US7105724B2 (en) 1997-04-04 2006-09-12 Board Of Regents Of University Of Nebraska Methods and materials for making and using transgenic dicamba-degrading organisms
US6791014B2 (en) 2000-08-11 2004-09-14 Aventis Cropscience, S.A. Use of HPPD inhibitors as selection agents in plant transformation
WO2002015701A2 (fr) 2000-08-25 2002-02-28 Syngenta Participations Ag Nouvelles toxines insecticides derivees de proteines cristallines insecticides de $i(bacillus thuringiensis)
WO2003018810A2 (fr) 2001-08-31 2003-03-06 Syngenta Participations Ag Toxines cry3a modifiees et sequences d'acides nucleiques les codant
WO2003052073A2 (fr) 2001-12-17 2003-06-26 Syngenta Participations Ag Nouvel evenement du mais
WO2004055191A1 (fr) 2002-12-17 2004-07-01 Biogemma Expression de la dioxygenase du pyruvate d'hydroxyphenyle dans les plastes de plantes pour la tolerance aux herbicides
WO2005107437A2 (fr) 2004-04-30 2005-11-17 Dow Agrosciences Llc Nouveaux genes de resistance aux herbicides
WO2006060634A2 (fr) 2004-12-01 2006-06-08 Basf Agrochemical Products, B.V. Nouvelle mutation impliquee dans l'accroissement de la resistance aux herbicides d'imidazolinone dans les plantes
US20080052798A1 (en) 2006-03-09 2008-02-28 E.I. Du Pont De Nemours And Company Polynucleotide Encoding a Maize Herbicide Resistance Gene and Methods for Use
US20090105077A1 (en) 2006-10-16 2009-04-23 Monsanto Technology Llc Methods and compositions for improving plant health
WO2008051633A2 (fr) 2006-10-25 2008-05-02 Monsanto Technology Llc Systèmes de culture destinés à lutter contre les mauvaises herbes
WO2013162077A1 (fr) 2012-04-27 2013-10-31 Sumitomo Chemical Company, Limited Composés de tétrazolinone et leur utilisation
WO2013162072A1 (fr) 2012-04-27 2013-10-31 Sumitomo Chemical Company, Limited Composés de tétrazolinone et leur utilisation en tant que pesticides
WO2014051165A1 (fr) 2012-09-28 2014-04-03 Sumitomo Chemical Company, Limited Composés de tétrazolinone et leur utilisation comme pesticides
WO2014051161A1 (fr) 2012-09-28 2014-04-03 Sumitomo Chemical Company, Limited Composés tétrazolinone et leur utilisation en tant que pesticide
WO2014084223A1 (fr) 2012-11-29 2014-06-05 住友化学株式会社 Composé de tétrazolinone et son utilisation

Non-Patent Citations (8)

* Cited by examiner, † Cited by third party
Title
BROWNING: "Agglomeration", CHEMICAL ENGINEERING, 4 December 1967 (1967-12-04), pages 147 - 48
FUNKE ET AL., PNAS, vol. 103, 2006, pages 13010 - 13015
HANCE ET AL.: "Weed Control Handbook, 8th Ed.,", 1989, BLACKWELL SCIENTIFIC
HECK, CROP SCI., vol. 45, 2005, pages 329 - 339
KLINGMAN: "Weed Control as a Science", 1961, J. WILEY & SONS
MOLLET, H.; GRUBEMANN, A.: "Formulation Technology", 2001, WILEY VCH VERLAG
PERRY'S: "Chemical Engineer's Handbook, 4th Ed.,", 1963, MCGRAW-HILL, pages: 8 - 57
PEST MANAGEMENT SCIENCE, vol. 61, 2005, pages 277 - 285

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10779536B2 (en) 2014-11-07 2020-09-22 Basf Se Pesticidal mixtures
US12302901B2 (en) 2014-11-07 2025-05-20 Basf Se Pesticidal mixtures
US11425909B2 (en) 2016-03-16 2022-08-30 Basf Se Use of tetrazolinones for combating resistant phytopathogenic fungi on fruits
US11241012B2 (en) 2016-03-16 2022-02-08 Basf Se Use of tetrazolinones for combating resistant phytopathogenic fungi on soybean
US10905122B2 (en) 2016-03-16 2021-02-02 Basf Se Use of tetrazolinones for combating resistant phytopathogenic fungi on cereals
CN109788758A (zh) * 2016-09-13 2019-05-21 巴斯夫欧洲公司 杀虫混合物
WO2018050508A1 (fr) * 2016-09-13 2018-03-22 Basf Se Mélanges pesticides
US10959431B2 (en) 2016-10-10 2021-03-30 Basf Se Pesticidal mixtures
EP3338552A1 (fr) * 2016-12-21 2018-06-27 Basf Se Utilisation d'un fongicide tetrazolinone sur des plantes transgéniques
WO2019052898A1 (fr) * 2017-09-13 2019-03-21 Basf Se Nouvelles formulations agrochimiques
EP3616516A1 (fr) * 2018-08-31 2020-03-04 Sumitomo Chemical Company, Limited Composition de lutte de maladies végétales et procédé de lutte de maladies végétales
EP3616517A1 (fr) * 2018-08-31 2020-03-04 Sumitomo Chemical Company, Limited Composition et procédé de lutte contre les maladies des plantes
EP3616515A1 (fr) * 2018-08-31 2020-03-04 Sumitomo Chemical Company, Limited Composition et procédé de lutte contre les maladies des plantes

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