DE3444860A1 - Selective herbicide - Google Patents
Selective herbicideInfo
- Publication number
- DE3444860A1 DE3444860A1 DE19843444860 DE3444860A DE3444860A1 DE 3444860 A1 DE3444860 A1 DE 3444860A1 DE 19843444860 DE19843444860 DE 19843444860 DE 3444860 A DE3444860 A DE 3444860A DE 3444860 A1 DE3444860 A1 DE 3444860A1
- Authority
- DE
- Germany
- Prior art keywords
- active ingredient
- formula
- active ingredients
- active
- combination
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
- 239000004009 herbicide Substances 0.000 title claims description 10
- 230000002363 herbicidal effect Effects 0.000 title abstract description 10
- ADZSGNDOZREKJK-UHFFFAOYSA-N 4-amino-6-tert-butyl-3-ethylsulfanyl-1,2,4-triazin-5-one Chemical compound CCSC1=NN=C(C(C)(C)C)C(=O)N1N ADZSGNDOZREKJK-UHFFFAOYSA-N 0.000 claims abstract description 4
- BTWJOUJEKBEAIW-UHFFFAOYSA-N trimethylsilylmethyl 2-[4-(3,5-dichloropyridin-2-yl)oxyphenoxy]propanoate Chemical compound C1=CC(OC(C)C(=O)OC[Si](C)(C)C)=CC=C1OC1=NC=C(Cl)C=C1Cl BTWJOUJEKBEAIW-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000004480 active ingredient Substances 0.000 claims description 51
- 241000196324 Embryophyta Species 0.000 claims description 27
- 239000003795 chemical substances by application Substances 0.000 claims description 4
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- 238000002360 preparation method Methods 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- 244000045561 useful plants Species 0.000 claims 3
- 238000000034 method Methods 0.000 claims 2
- 239000013543 active substance Substances 0.000 abstract description 2
- 230000006378 damage Effects 0.000 description 9
- -1 3,5-dichloropyridin-2-oxy Chemical group 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
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- 150000001875 compounds Chemical class 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
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- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical group O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
Mittel zur selektiven UnkrautbekämpfungSelective weed control agents
Die vorliegende Erfindung betrifft eine neue Wirkstoffkombination, die aus einem bekannten Pyridoxy-phenoxypropionsäure-Derivat einerseits und aus einem bekannten Triazinon andererseits besteht und besonders gut zur selektiven Unkrautbekämpfung in Nutzpflanzenkulturen geeignet ist.The present invention relates to a new combination of active ingredients from a known pyridoxyphenoxypropionic acid derivative on the one hand and from a well-known triazinon on the other hand and particularly good for selective Weed control in crops of useful plants is suitable.
Es ist bereits bekannt geworden, daß 2-/4-(3,5-Dichlorpyridin-2-oxy) -phenoxy7-propionsäure- (trimethylsilyl)-methylester herbizide Wirksamkeit besitzt (vgl. EP-OS 0 096 354). Weiterhin ist bekannt, daß sich Unkräuter mit Hilfe von 4-Amino-6-tert.-butyl-3-ethylthio-1,2,4-triazin-5(4H)-on selektiv bekämpfen lassen (vgl. US-PS 3 671 523). Die genannten Stoffe zeichnen sich durch eine gute selektive herbizide Wirksamkeit aus, jedoch läßt die Verträglichkeit gegenüber Kulturpflanzen in manchen Fällen zu wünschen übrig.It is already known that 2- / 4- (3,5-dichloropyridin-2-oxy) -phenoxy7-propionic acid (trimethylsilyl) methyl ester has herbicidal activity (see EP-OS 0 096 354). It is also known that weeds with the help of Let 4-amino-6-tert-butyl-3-ethylthio-1,2,4-triazin-5 (4H) -one be combated selectively (See U.S. Patent 3,671,523). The substances mentioned are characterized by a good selective herbicidal activity, but leaves the tolerance to crop plants in some cases much to be desired.
Es wurde nun gefunden, daß die neue Wirkstoffkombination aus (a) 2-[4-(3,5-Dichlor-pyridin-2-oxy)-phenoxy]-propionsäure- (trimethylsilyl? -methylester der Formel und (b) 4-Amino-6-tert.-butyl-3-ethylthio-1,2,4-triazin-5(4H)-on der Formel eine besonders gute selektive herbizide Wirksamkeit aufweist.It has now been found that the new active ingredient combination of (a) 2- [4- (3,5-dichloro-pyridin-2-oxy) -phenoxy] -propionic acid (trimethylsilyl? -Methyl ester of the formula and (b) 4-amino-6-tert-butyl-3-ethylthio-1,2,4-triazin-5 (4H) -one of the formula has a particularly good selective herbicidal effectiveness.
Uberraschenderweise ist die Verträglichkeit der erfindungsgemäßen Wirkstoffkombination gegenüber Kulturpflanzen deutlich höher als die Summe der Verträglichkeiten der einzelnen Wirkstoffe. Es liegt also ein nicht vorhersehbarer antagonistischer Effekt und nicht nur eine Wirkungsergänzung vor.Surprisingly, the compatibility of the invention The combination of active ingredients compared to crop plants is significantly higher than the sum of the tolerances of the individual active ingredients. So there is an unpredictable antagonistic Effect and not just a supplement.
Die Verbindung der Formel (I) enthält ein asymmetrisch substituiertes Kohlenstoffatom in der PropionsAure-Einheit und kann deshalb in zwei enantiomeren Formen vorliegen. Die Erfindung betrifft sowohl eine Wirkstoffkombination, welche das Racemat der Verbindung der Formel (I) enthält, als auch eine Wirkstoffkombination, welche das R-Enantiomere*) der Verbindung der Formel (I) enthält.The compound of the formula (I) contains an asymmetrically substituted one Carbon atom in the propionic acid unit and can therefore be in two enantiomers to shape are present. The invention relates to both an active ingredient combination, which contains the racemate of the compound of formula (I), as well as a combination of active ingredients, which contains the R enantiomer *) of the compound of the formula (I).
Die in der erfindungsgemäßen Wirkstoffkombination enthaltenen Wirkstoffe sind bereits bekannt (vgl. EP-OS 0 096 354 und US-PS 3 671 523).The active ingredients contained in the active ingredient combination according to the invention are already known (cf. EP-OS 0 096 354 and US-PS 3,671,523).
Der antagonistische Effekt der erfindungsgemäßen Wirkstoffkombination zeigt sich vor allem dann, wenn die Wirkstoffe der Formeln (I) und (II) in bestimmten Gewichtsverhältnissen vorhanden sind. Jedoch können die Gewichtsverhältnisse in der Wirkstoffkombination in relativ großen Bereichen variiert werden. Im allgemeinen entfallen auf 1 Gewichtsteil an Wirkstoff der Formel (II) 0,01 bis 0,6 Gewichtsteile, vorzugsweise 0,05 bis 0,5 Gewichtsteile an Wirkstoff der Formel (I).The antagonistic effect of the active ingredient combination according to the invention shows up especially when the active ingredients of formulas (I) and (II) in certain Weight ratios are available. However, the weight ratios in the combination of active ingredients can be varied over a relatively wide range. In general allotted to 1 part by weight of active ingredient of the formula (II) 0.01 to 0.6 parts by weight, preferably 0.05 to 0.5 parts by weight of active ingredient of the formula (I).
Die erfindungsgemäße Wirkstoffkombination zeigt eine sehr gute Wirkung gegen Unkräuter und Ungräser in Nutzpflanzenkulturen, insbesondere in Getreide. Unter Unkräutern und Ungräsern im weitesten Sinne sind alle Pflanzen zu verstehen, die an Orten wachsen, wo sie unerwünscht sind.The active ingredient combination according to the invention shows a very good effect against weeds and grass weeds in crops of useful plants, in particular in cereals. Weeds and grass weeds in the broadest sense are all plants that grow in places where they are undesirable.
*) Unter dem R-Enantiomeren ist im vorliegenden Fall diejenige optisch aktive Verbindung der Formel (I) zu verstehen, die am asymmetrisch substituierten Kohlenstoffatom der Propionsäure-Einheit die R-Konfiguration aufweist.*) In the present case, the R enantiomer is optical active compound of formula (I) to understand the most asymmetrically substituted Carbon atom of the propionic acid unit has the R configuration.
Die erfindungsgemäße Wirkstoffkombination kann z.B.The active ingredient combination according to the invention can e.g.
bei den folgenden Pflanzen verwendet werden: Dikotyle Unkräuter der Gattungen: Sinapis, Lepidium, Galium, Stellaria, Matricaria, Anthemis, Galinsoga, Chenopodium, Urtica, Senecio, Amaranthus, Portulaca, Xanthium, Convolvulus, Ipomoea, Polygonum, Sesbania, Ambrosia, Cirsium, Carduus, Sonchus, Solanum, Rorippa, Rotala, Lindernia, Lamium, Veronica, Abutilon, Emex, Datura, Viola, Galeopsis, Papaver, Centaurea.be used in the following plants: dicot weeds the Genera: Sinapis, Lepidium, Galium, Stellaria, Matricaria, Anthemis, Galinsoga, Chenopodium, Urtica, Senecio, Amaranthus, Portulaca, Xanthium, Convolvulus, Ipomoea, Polygonum, Sesbania, Ambrosia, Cirsium, Carduus, Sonchus, Solanum, Rorippa, Rotala, Lindernia, Lamium, Veronica, Abutilon, Emex, Datura, Viola, Galeopsis, Papaver, Centaurea.
Dikotyle Kulturen der Gattungen: Gossypium, Glycine, Beta, Daucus, Phaseolus, Pisum, Solanum, Linum, Ipomoea, Vicia, Nicotiana, Lycopersicon, Arachis, Brassica, Lactuca, Cucumis, Cucurbita.Dicot cultures of the genera: Gossypium, Glycine, Beta, Daucus, Phaseolus, Pisum, Solanum, Linum, Ipomoea, Vicia, Nicotiana, Lycopersicon, Arachis, Brassica, Lactuca, Cucumis, Cucurbita.
Monokotyle Unkräuter der Gattungen. Echinochloa, Setaria, Panicum, Digitaria, Phleum, Poa, Festuca, Eleusine, Brachiaria, Lolium, Bromus, Avena, Cyperus, Sorghum, Agropyron, Cynodon, Monochoria, Fimbristylis, Sagittaria, Eleocharis, Scirpus, Paspalum, Ischaemum, Sphenoclea, Dactyloctenium, Agrostis e Alopecurus, Apera.Monocot weeds of the genera. Echinochloa, Setaria, Panicum, Digitaria, Phleum, Poa, Festuca, Eleusine, Brachiaria, Lolium, Bromus, Avena, Cyperus, Sorghum, Agropyron, Cynodon, Monochoria, Fimbristylis, Sagittaria, Eleocharis, Scirpus, Paspalum, Ischaemum, Sphenoclea, Dactyloctenium, Agrostis e Alopecurus, Apera.
Monokotyle Kulturen der Gattungen: Oryza, Zea, Triticum, Hordeum, Avena, Secale, Sorghum, Panicum, Saccharum, Ananas, Asparagus, Allium.Monocot cultures of the genera: Oryza, Zea, Triticum, Hordeum, Avena, Secale, Sorghum, Panicum, Saccharum, Ananas, Asparagus, Allium.
Die Verwendung der erfindungsgemäßen Wirkstoffe ist jedoch keineswegs auf diese Gattungen beschränkt, sondern erstreckt sich in gleicher Weise auch auf andere Pflanzen.However, the use of the active ingredients according to the invention is by no means limited to these genera, but extends in the same way to other plants.
Der Einsatz der erfindungsgemäßen Wirkstoffkombination zur selektiven Unkrautbekämpfung ist vorzugsweise möglich in Getreidekulturen, wie zum Beispiel Weizen und Gerste.The use of the active ingredient combination according to the invention for selective Weed control is preferably possible in cereal crops, such as Wheat and barley.
Die Wirkstoffkombination kann in die üblichen Formulierungen übergeführt werden, wie Lösungen, Emulsionen, Spritzpulver, Suspensionen, Pulver, Stäubemittel, Pasten, lösliche Pulver, Granulate, Suspensions-Emulsions-Konzentrate, Wirkstoff-imprägnierte Natur- und synthetische Stoffe, Feinstverkapselungen in polymeren Stoffen.The combination of active ingredients can be converted into the usual formulations such as solutions, emulsions, wettable powders, suspensions, powders, dusts, Pastes, soluble powders, granules, suspension-emulsion concentrates, active ingredient-impregnated Natural and synthetic materials, finest encapsulation in polymer materials.
Diese Formulierungen werden in bekannter Weise hergestellt, z.B. durch Vermischen der Wirkstoffe mit Streckmitteln, also flüssigen Lösungsmitteln, unter Druck stehenden verflüssigten Gasen und/oder festen Trägerstoffen, gegebenenfalls unter Verwendung von oberflächenaktiven Mitteln, also Emulgiermitteln und/oder Dispergiermitteln und/oder schaumerzeugenden Mitteln.These formulations are prepared in a known manner, e.g. Mixing the active ingredients with extenders, i.e. liquid solvents, under Liquefied gases under pressure and / or solid carriers, if appropriate using surface-active agents, i.e. emulsifiers and / or dispersants and / or foam-generating agents.
Im Falle der Benutzung von Wasser als Streckmittel können z.B. auch organische Lösungsmittel als Hilfslösungsmittel verwendet werden. Als flüssige Lösungsmittel kommen im wesentlichen in Frage: Aromaten, wie Xylol, Toluol oder Alkylnaphthaline, chlorierte Aromaten oder chlorierte aliphatische Kohlenwasserstoffe, wie Chlorbenzole, Chlorethylene oder Methylenchlorid, aliphatische Kohlenwasserstoffe, wie Cyclohexan oder Paraffine, z.B. Erdölfraktionen, Alkohole, wie Butanol oder Glycol sowie deren Ether und Ester, Ketone, wie Aceton, Methylethylketon, Methylisobutylketon oder Cyclohexanon, stark polare Lösungsmittel, wie Dimethylformamid und Dimethylsulfoxid, sowie Wasser.In the case of using water as an extender, e.g. organic solvents can be used as auxiliary solvents. As a liquid solvent are essentially: aromatics, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons, such as chlorobenzenes, Chlorethylene or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, e.g. petroleum fractions, alcohols such as butanol or glycol and their Ethers and esters, ketones, such as Acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, as well as water.
Als feste Trägerstoffe kommen in Frage: z.B. natürliche Gesteinsmehle, wie Kaoline, Tonerden, Talkum, Kreide, Quarz, Attapulgit, Montmorillonit oder Diatomeenerde und synthetische Gesteinsmehle, wie hochdisperse Kieselsäure, Aluminiumoxid und Silikate; als feste Trägerstoffe für Granulate kommen in Frage: z.B. gebrochene und fraktionierte natürliche Gesteine wie Calcit, Marmor, Bims, Sepiolith, Dolomit sowie synthetische Granulate aus anorganischen und organischen Mehlen sowie Granulate aus organischem Material wie Sägemehl, Kokosnußschalen, Maiskolben und Tabakstengel; als Emulgier- und/oder schaumerzeugende Mittel kommen in Frage: z.B. nichtionogene und anionische Emulgatoren, wie Polyoxyethylen-Fettsäure-Ester, Polyoxyethylen-Fettalkohol-Ether, z.B. Alkylarylpolyglykolether, Alkylsulfonate, Alkylsulfate, Arylsulfonate sowie Eiweißhydrolysate; als Dispergiermittel kommen in Frage: z.B. Lignin-Sulfitablaugen und Methylcellulose.The following can be used as solid carriers: e.g. natural rock flour, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic minerals such as fumed silica, alumina and Silicates; Solid carriers for granulates are: e.g. broken ones and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite as well as synthetic granules made from inorganic and organic flours and granules made of organic material such as sawdust, coconut shells, corn on the cob, and tobacco stalks; as emulsifying and / or foam-generating agents come into question: e.g. non-ionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, e.g. alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, aryl sulfonates and Protein hydrolysates; Possible dispersants are: e.g. lignin sulphite waste liquors and methyl cellulose.
Als weitere Zusätze kommen oberflächenaktive Stoffe in Betracht. Vorzugsweise verwendbar sind Lecithine, Phospholipide, Isopropylmyristat und die unter den Bezeichnungen Agridex, Azone, Surfactant WK und Emulgator OX bekannten Substanzen.Surface-active substances come into consideration as further additives. Preferably lecithins, phospholipids, isopropyl myristate and those under the names can be used Agridex, Azone, Surfactant WK and Emulsifier OX are known substances.
Es können in den Formulierungen Haftmittel wie Carboxymethylcellulose, natürliche und synthetische pulverige körnige oder latexförmige Polymere verwendet werden, wie Gummiarabicum, Polyvinylalkohol, Polyvinylacetat.Adhesives such as carboxymethyl cellulose, natural and synthetic powdery granular or latex-shaped Polymers are used, such as gum arabic, polyvinyl alcohol, polyvinyl acetate.
Es können Farbstoffe wie anorganische Pigmente, z.B Eisenoxid, Titanoxid, Ferrocyanblau und organische Farbstoffe, wie Alizarin-, Azo- und Metallphthalocyaninfarbstoffe und Spurennährstoffe wie Salze von Eisen, Mangan, Bor, Kupfer, Kobalt, Molybdän und Zink verwendet werden.Dyes such as inorganic pigments, e.g. iron oxide, titanium oxide, Ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc can be used.
Die Formulierungen enthalten im allgemeinen zwischen 0,1 und 95 Gew.-% Wirkstoff, vorzugsweise zwischen 0,5 und 90 %.The formulations generally contain between 0.1 and 95% by weight Active ingredient, preferably between 0.5 and 90%.
Die erfindungsgemäße Wirkstoffkombination kann als solche oder in ihren Formulierungen auch in Mischung mit bekannten Herbiziden zur Unkrautbekämpfung Verwendung finden, wobei Fertigformulierung oder Tankmischung möglich ist. Auch eine Mischung mit anderen bekannten Wirkstoffen, wie Fungiziden, Insektiziden, Akariziden, Nematiziden, Schutzstoffen gegen Vogelfraß, Wuchsstoffen, Pflanzennährstoffen und Bodenstrukturverbesserungsmitteln ist möglich.The active ingredient combination according to the invention can be used as such or in their formulations also mixed with known herbicides for weed control Find use, finished formulation or tank mixing is possible. Even a mixture with other known active ingredients, such as fungicides, insecticides, acaricides, Nematicides, bird repellants, growth substances, plant nutrients and Soil structure improvers is possible.
Die Wirkstoffkombination kann als solche, in Form ihrer Formulierungen oder den daraus durch weiteres Verdünnen bereiteten Anwendungsformen, wie gebrauchsfertige Lösungen, Suspensionen, Emulsionen, Pulver, Pasten und Granulate angewandt werden. Die Anwendung geschieht in üblicher Weise, z.B. durch Gießen, Spritzen, Sprühen, Streuen.The active ingredient combination can be used as such, in the form of their formulations or the use forms prepared therefrom by further dilution, such as ready-to-use Solutions, suspensions, emulsions, powders, pastes and granulates can be used. It is used in the usual way, e.g. by watering, squirting, atomizing, Sprinkle.
Die erfindungsgemäße Wirkstoffkombination kann sowohl vor als auch nach dem Auflaufen der Pflanzen appliziert werden. Sie kann auch vor der Saat in den Boden eingearbeitet werden.The active ingredient combination according to the invention can both before and be applied after the plants emerge. It can also be pre-sown in be incorporated into the floor.
Die aufgewandte Wirkstoffmenge kann in größeren Bereichen schwanken. Sie hängt im wesentlichen von der Art des gewünschten Effekts ab. Im allgemeinen liegen die Aufwandmengen zwischen 0,1 und 5 kg Wirkstoff pro ha, vorzugsweise zwischen 0,5 und 2,5 kg/ha.The amount of active ingredient used can fluctuate over a wide range. It essentially depends on the type of effect you want. In general the application rates are between 0.1 and 5 kg of active ingredient per hectare, preferably between 0.5 and 2.5 kg / ha.
Die gute herbizide Wirkung und die ausgezeichnete Pflanzenverträgl ichkeit der erfindungsgemäßen Wirkstoffkombination geht aus dem nachfolgenden Beispiel hervor.The good herbicidal effect and the excellent plant tolerance The following example shows the effectiveness of the active ingredient combination according to the invention emerged.
Während die einzelnen Wirkstoffe Schwächen in der Pflanzenverträglichkeit aufweisen, zeigt die Kombination eine Pflanzenverträglichkeit, die über eine einfache Wirkungssummierung hinausgeht.While the individual active ingredients have weaknesses in plant tolerance have, the combination shows a plant tolerance that is higher than a simple Effect summation goes beyond.
Ein antagonistischer Effekt liegt bei Herbiziden immer dann vor, wenn die Pflanzenverträglichkeit der Wirkstoffkombination besser ist als die der einzeln applizierten Wirkstoffe und gleichzeitig die herbizide Potenz nicht beeinträchtigt wird.With herbicides, there is always an antagonistic effect when the plant tolerance of the active ingredient combination is better than that of the individual applied active ingredients and at the same time the herbicidal potency is not impaired will.
Die zu erwartende Wirkung für eine gegebene Kombination zweier Herbizide kann (vgl. Colby, S. R., 'tCalculating synergistic and antagonistic responses of herbicide combinations", Weeds 15, Seiten 20-22, 1967) wie folgt berechnet werden: Wenn X = % Schädigung durch Herbizid A bei p kg/ha Aufwandmenge und Y = % Schädigung durch Herbizid B bei q kg/ha Aufwandmenge und E = die erwartete Schädigung der Herbizide A und B bei p und q kg/ha Aufwandmenge bedeutet, dann ist E = X + Y - X . Y 100 Ist die tatsächliche Schädigung der Kulturpflanzen kleiner als berechnet, so ist die Kombination in ihrer Wirkung nicht additiv; d.h. es liegt ein antagonistischer Effekt vor.The expected effect for a given combination of two herbicides can (cf. Colby, S. R., 'tCalculating synergistic and antagonistic responses of herbicide combinations ", Weeds 15, pages 20-22, 1967) can be calculated as follows: if X =% damage by herbicide A at p kg / ha application rate and Y =% damage by herbicide B at q kg / ha application rate and E = the expected damage to the herbicides A and B at p and q mean the application rate, then E = X + Y - X. Y 100 If the actual damage to the cultivated plants is less than calculated, then the effect of the combination is not additive; i.e. there is an antagonistic one Effect before.
Wie aus dem nachfolgenden Beispiel hervorgeht, ist die schädigende Wirkung der erfindungsgemäßen Wirkstoffkombination bei den Kulturpflanzen kleiner als die berechnete. Es ist also ein echter antagonistischer Effekt vorhanden.As can be seen from the example below, the is damaging The effect of the active compound combination according to the invention on the crop plants is smaller than the calculated. So there is a real antagonistic effect.
Beispiel A Post-emergence-Test / Freiland Lösungsmittel: 5 Gew.-Teile Aceton Emulgator: 1 Gew.-Teil Alkylarylpolyglykolether Zur Herstellung einer zweckmäßigen Wirkstoffzubereitung vermischt man 1 Gew.-Teil Wirkstoff bzw. Wirkstoffgemisch mit der angegebenen Menge Lösungsmittel, gibt die angegebene Menge Emulgator zu und verdünnt das Konzentrat mit Wasser auf die gewünschte Konzentration.Example A Post-emergence test / field solvent: 5 parts by weight Acetone emulsifier: 1 part by weight of alkylaryl polyglycol ether Active ingredient preparation is mixed with 1 part by weight of active ingredient or active ingredient mixture the specified amount of solvent, adds the specified amount of emulsifier and dilutes the concentrate with water to the desired concentration.
Im Freiland werden Testpflanzen, welche eine Höhe von 3 bis 10 cm haben, mit der jeweiligen Wirkstoffzubereitung so bespritzt, daß die jeweils gewünschte Wirkstoffmenge pro Flächeneinheit ausgebracht wird. Die Konzentration der Spritzbrühe wird so gewählt, daß in 2000 1 Wasser/ha die jeweils gewünschte Wirkstoffmenge ausgebracht wird.In the field, test plants that are 3 to 10 cm in height are used have, sprayed with the respective active ingredient preparation so that the particular desired Amount of active ingredient per unit area is applied. The concentration of the spray liquid is chosen so that the particular amount of active compound desired is applied in 2,000 l of water / ha will.
Nach drei Wochen wird der Schädigungsgrad der Pflanzen bonitiert in % Schädigung im Vergleich zur Entwicklung der unbehandelten Kontrolle. Es bedeuten: 0 % keine Wirkung (wie unbehandelte Kontrolle) 100 % totale Vernichtung.After three weeks, the degree of damage to the plants is rated in % Damage compared to the development of the untreated control. It means: 0% no effect (like untreated control) 100% total destruction.
In diesem Test zeigt die erfindungsgemäße Wirkstoffkombination eine Pflanzenverträglichkeit, die besser ist als Pflanzenverträglichkeit der einzelnen Wirkstoffe.In this test, the active ingredient combination according to the invention shows a Plant tolerance that is better than the plant tolerance of the individual Active ingredients.
Wirkstoffe, Wirkstoffkonzentrationen und Versuchsergebnisse gehen aus der folgenden Tabelle hervor.Active ingredients, active ingredient concentrations and test results go from the following table.
Tabelle A Post-emergence-Test /Freiland
Claims (5)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19843444860 DE3444860A1 (en) | 1984-12-08 | 1984-12-08 | Selective herbicide |
| GB08529619A GB2167959B (en) | 1984-12-08 | 1985-12-02 | Combination of pyridoxyphenoxypropionate and triazinone as selective weed killer |
| FR8518159A FR2574249A1 (en) | 1984-12-08 | 1985-12-06 | HERBICIDE COMPOSITION CONTAINING A PYRIDOXY-PHENOXY-PROPIONIC ACID DERIVATIVE AND A TRIAZINONE AND ITS APPLICATION TO SELECTIVE WEED CONTROL |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19843444860 DE3444860A1 (en) | 1984-12-08 | 1984-12-08 | Selective herbicide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE3444860A1 true DE3444860A1 (en) | 1986-06-12 |
Family
ID=6252274
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19843444860 Withdrawn DE3444860A1 (en) | 1984-12-08 | 1984-12-08 | Selective herbicide |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE3444860A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0823995A1 (en) * | 1996-08-12 | 1998-02-18 | Hoechst Schering AgrEvo GmbH | Synergistic combinations of active substances for the control of weeds in cultures of useful plant |
-
1984
- 1984-12-08 DE DE19843444860 patent/DE3444860A1/en not_active Withdrawn
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0823995A1 (en) * | 1996-08-12 | 1998-02-18 | Hoechst Schering AgrEvo GmbH | Synergistic combinations of active substances for the control of weeds in cultures of useful plant |
| US6316387B1 (en) | 1996-08-12 | 2001-11-13 | Hoechst Schering Agrevo Gmbh | Synergistic active compound combinations for controlling harmful plants in crops of useful plants |
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| Date | Code | Title | Description |
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