US20050020640A1 - Method of controlling soil insects with phenylpyrazoles - Google Patents

Method of controlling soil insects with phenylpyrazoles Download PDF

Info

Publication number
US20050020640A1
US20050020640A1 US10/893,902 US89390204A US2005020640A1 US 20050020640 A1 US20050020640 A1 US 20050020640A1 US 89390204 A US89390204 A US 89390204A US 2005020640 A1 US2005020640 A1 US 2005020640A1
Authority
US
United States
Prior art keywords
alkyl
compositions according
insecticidal compositions
haloalkyl
radical
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.)
Abandoned
Application number
US10/893,902
Inventor
Jean-Michael Gaulliard
Christian Segaud
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF Agro BV Arnhem NL Zweigniederlassung Freienbach
Original Assignee
BASF Agro BV Arnhem NL Zweigniederlassung Waedenswil
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 Agro BV Arnhem NL Zweigniederlassung Waedenswil filed Critical BASF Agro BV Arnhem NL Zweigniederlassung Waedenswil
Priority to US10/893,902 priority Critical patent/US20050020640A1/en
Publication of US20050020640A1 publication Critical patent/US20050020640A1/en
Assigned to BASF AGRO B.V., ARNHEM (NL), WADENSWIL-BRANCH reassignment BASF AGRO B.V., ARNHEM (NL), WADENSWIL-BRANCH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: AVENTIS CROPSCIENCE SA
Abandoned legal-status Critical Current

Links

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
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/561,2-Diazoles; Hydrogenated 1,2-diazoles
    • 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
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/002Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing a foodstuff as carrier or diluent, i.e. baits
    • A01N25/006Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing a foodstuff as carrier or diluent, i.e. baits insecticidal
    • 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
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/02Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom

Definitions

  • the subject of the present invention is novel compositions intended for controlling soil insects in their various developmental forms, and in particular compositions useful for controlling click beetles.
  • the invention also relates to a method of control using the said compositions.
  • Insecticidal compounds of the phenylpyrazole type which can be used in controlling insects are known in particular from patent applications EP 295117, WO 87/3781, 93/6089 and 94/21606.
  • Patent applications EP 295117 and 836386 also mention compositions comprising from 0.01% to 5% of such active substances.
  • Click beetles constitute a family of insects which are particularly harmful for certain crops, more particularly for maize, beet, sunflower, potato and rape crops. Their harmful character is all the more marked since the larval forms of click beetles can remain for very long periods in the soil, extending up to 5 years.
  • Baits have indeed been proposed for various sorts of insects, as well as formulas which can be consumed by ingestion, but these formulas are not necessarily active for all the types of insect and the need remains to find insecticidal forms or formulations which are particularly effective for the most diverse applications, and in particular for controlling click beetles.
  • insecticides applied over or into the soil it is desirable to find conditions and formulations which make it possible to obtain good efficacy at doses which are as low as possible.
  • One aim of the invention is to overcome these difficulties completely or in part.
  • Another aim of the invention is to provide advantageous and effective compositions for controlling non-gregarious insects.
  • Another aim of the invention is to provide advantageous and effective compositions for controlling soil insects, especially click beetles, and more particularly click beetles in the larval state.
  • Another aim of the invention is to provide compositions comprising at least one insecticidal active substance of the phenylpyrazole type and which are easily applicable over or into the soil.
  • Another aim of the invention is to provide insecticide compositions whose performance is good in spite of low applicable doses.
  • compositions comprising:
  • the alkyl radicals of the definition of formula (I) generally comprise from 1 to 6 carbon atoms.
  • the ring formed by the divalent alkylene radical representing R 5 and R 6 as well as by the nitrogen atom to which R 5 and R 6 are attached is generally a 5-, 6- or 7-membered ring.
  • the compound of formula (I) may be prepared according to one of the methods described in patent applications WO 87/3781, 93/6089, 94/21606, EP 295117 or alternatively by another method within the general knowledge of persons skilled in the art competent in chemical synthesis. This compound is generally designated in the present text by the term active substance.
  • the meals which can be used, there may be mentioned the meals derived from the grinding of cereal grains such as wheat, barley, rye, triticale, oats, or also rice, sorghum, soyabean, maize, the preferred meal being that based on maize.
  • cereal grains such as wheat, barley, rye, triticale, oats, or also rice, sorghum, soyabean, maize.
  • the preferred meal being that based on maize.
  • a mixture of these vegetable meals can also be envisaged in the context of the present invention.
  • the moisture-retaining agents of an organic nature there may be mentioned the macromolecular hydrophilic derivatives of plant origin, and in particular the cellulosic hydrophilic derivatives, and more particularly cellulose, but also one or more disintegrating agents. It may be advantageous to use these compounds in particular when meals such as hard wheat meals are used in the granules.
  • Disintegrating agents include: starch, sodium carboxymethyl starch, cellulose such as microcrystalline cellulose; modified celluloses such as sodium carboxymethylcellulose; bentonite, aluminium and magnesium silicate; sodium polynaphthalenesulphonate, sodium dodecylbenzenesulphonate, sodium dioctylsulphosuccinate, lignin sulphonate; a saccharide derivative such as lactose, fructose, sucrose, mannitol, dextrose; a cross-linked derivative of polyvinylpyrrolidone.
  • the composition according to the invention may contain from 0.5 to 30%, and preferably from 1 to 20%, by weight of the dry substance, of the said agent(s).
  • the composition also comprises from 3 to 30%, preferably from 4 to 20% of sugars.
  • the sugars are chosen in particular from mono-, oligo- or polyorganosaccharides, especially from sucrose, lactose, fructose, dextrose, glucose or alternatively molasses or honey.
  • compositions which are the subject of the invention may also comprise a preservative preventing the degradation of the meals, such as sodium benzoate, 1,2-benzisothiazolin-3-one, benzoic acid, para-hydroxybenzoic acid and its ester derivatives and its alkali or alkaline-earth metal salts, in particular the sodium salt, 2-phenylphenol and its alkali or alkaline-earth metal salts, in particular the sodium salt, para-nitrophenol.
  • a preservative preventing the degradation of the meals such as sodium benzoate, 1,2-benzisothiazolin-3-one, benzoic acid, para-hydroxybenzoic acid and its ester derivatives and its alkali or alkaline-earth metal salts, in particular the sodium salt, 2-phenylphenol and its alkali or alkaline-earth metal salts, in particular the sodium salt, para-nitrophenol.
  • additives may also be included such as colourings or attractants for pests or repellents for birds or animals which are useful or which should be protected.
  • formulation additives may be used such as binding, agglomerating, appetite-enhancing, agglutinating, gelling, swelling or antiadherent agents and the like.
  • a preferred class of compounds of formula (I) comprises compounds such that R 1 is CN, and/or R 3 is haloalkyl, and/or R 4 is NH 2 , and/or R 11 and R 12 are, independently of each other, a halogen atom, and/or R 13 is haloalkyl.
  • the compound of formula (I) used in the invention is 5-amino-3-cyano-1-[2,6-di-chloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)-sulphinyl]-1H-pyrazole, to which reference is made in the examples under the term “fipronil”.
  • the formulations according to the invention are generally in the form of granules.
  • the size of the granules is advantageously between 0.1 mm and 3 cm, preferably between 0.5 and 4 mm. These granules are advantageously insoluble in water (in the sense that they resist disintegration with water).
  • compositions according to the invention may be prepared by simply mixing the various constituents, preferably by extrusion or compression in the cold or hot state according to any granulation or pelleting technique known per se.
  • any granulation or pelleting technique known per se for the production of such granules, reference can be easily made to the European patent application published under the number EP 0575838 and/or to other techniques, for example extrusion techniques, known to persons skilled in the art.
  • the invention also relates to a method of protecting crops from insects, especially click beetles, characterized in that an effective quantity of a composition in the form of granules having a size of between 0.2 mm and 2 cm comprising an active substance chosen from the group consisting of the products of formula I, imidacloprid, acetamiprid, nitenpyram and thiamethoxam, is applied over or into the soil (preferably into the soil) of the area which has to be cultivated.
  • the invention thus relates more particularly to a method of protecting cereal, preferably maize or beet or sunflower or potato or rape, crops.
  • the application of the formulations according to the invention takes place advantageously before sowing the said crop, or simultaneously with this sowing.
  • the invention also relates to a method of controlling insects, especially click beetles, characterized in that an effective quantity of one of the compositions according to the invention is applied over or into the soil (preferably into the soil) where they are present or are likely to be present.
  • compositions corresponding to a dose of compound of formula (I) of between 1 and 50 g/ha, preferably between 3 and 40 g/ha are often used.
  • a specific characteristic of the method of controlling insects according to the invention consists in the application, over or into the soil, of a composition providing a dose which is nonlethal through contact but lethal through ingestion.
  • the method consists in killing the click beetles by application of a dose which is nonlethal through contact but lethal through ingestion.
  • a hypothesis for the good efficacy of the method of treatment according to the invention which makes it possible to greatly reduce the applicable doses of compounds of formula I in particular, is based on the fact that once the bait according to the invention has caused the death of a click beetle, the latter can itself serve as bait for other click beetles, which therefore also ingest a product (dead click beetle) containing the insecticide.
  • insecticide and insect should be taken in their broad ordinary sense and not in their strictly scientific (zoological) sense. Accordingly, the term insect is understood to mean any animal of a very small size such as arthropods (insects in the strict and zoological sense, arachnids, myriapods) and nematodes.
  • the Coleoptera (wireworms ( Agriotes spp.), false wireworms, white grubs) such as for example:
  • Diabrotica spp. cornrootworms, Crysomelidae
  • Tanymecus pallidus (beet leaf weevil, Curculionidae).
  • the Lepidoptera (Noctuidae) such as:
  • Autographa spp. Mamestra spp., Agrotis spp. (cutworms, grey grubs), Euxoa spp. (cutworms, grey grubs), Spodoptera spp. ( Spodoptera exigua, Spodoptera littorlis ).
  • the Diptera such as Tipula spp.).
  • the Myriapoda (Myriapoda):
  • the granules according to the invention are advantageously inserted into the soil at a depth of between 1 and 5 cm.
  • compositions according to the invention are particularly advantageous in that they allow the use of lower doses of active product than similar known compositions.
  • a surface of 0.1 ha is sown with maize at the rate of about 8000 untreated seeds. This surface is divided into 40-m 2 plots.
  • the soil is dug out and scraped in order to capture and identify the insects responsible for the damage; a large presence of larvae of click beetles of the genus Agriotes , in particular Agriotes sordidus , is observed for the untreated control.
  • a surface of 1 ha is sown with maize at the rate of about 98,100 untreated seeds. This surface is divided into 27-m 2 plots.
  • the soil is dug out and scraped in order to capture and identify the insects responsible for the damage; a large presence of larvae of click beetles of the genus Agriotes , in particular Agriotes lineatus.

Abstract

The invention concerns insecticide compositions comprising: a) between 0.001 and 5 %, preferable between 0.05 and 1% of a compound of the type 1-phenyl pyrazole, in particular 1-[2,6-Cl24-CF3 phenyl]3-CN4[SO—CF3]5-NH2 pyrazole ; and b) between 0.05 and 10%, preferably between 0.1 and 5% of one (or several) moisture retaining agent of the organic type; and c) between 40 and 99%, preferably between 50 and 98% (and more preferably between 70 and 97%) of vegetable flour. The invention also concerns a method for fighting insects using said composition, in particular against click beetles.

Description

  • The subject of the present invention is novel compositions intended for controlling soil insects in their various developmental forms, and in particular compositions useful for controlling click beetles. The invention also relates to a method of control using the said compositions.
  • Insecticidal compounds of the phenylpyrazole type which can be used in controlling insects are known in particular from patent applications EP 295117, WO 87/3781, 93/6089 and 94/21606. Patent applications EP 295117 and 836386 also mention compositions comprising from 0.01% to 5% of such active substances.
  • Click beetles constitute a family of insects which are particularly harmful for certain crops, more particularly for maize, beet, sunflower, potato and rape crops. Their harmful character is all the more marked since the larval forms of click beetles can remain for very long periods in the soil, extending up to 5 years.
  • Baits have indeed been proposed for various sorts of insects, as well as formulas which can be consumed by ingestion, but these formulas are not necessarily active for all the types of insect and the need remains to find insecticidal forms or formulations which are particularly effective for the most diverse applications, and in particular for controlling click beetles.
  • In addition, as regards the insecticides applied over or into the soil, it is desirable to find conditions and formulations which make it possible to obtain good efficacy at doses which are as low as possible.
  • One aim of the invention is to overcome these difficulties completely or in part.
  • Another aim of the invention is to provide advantageous and effective compositions for controlling non-gregarious insects.
  • Another aim of the invention is to provide advantageous and effective compositions for controlling soil insects, especially click beetles, and more particularly click beetles in the larval state.
  • Another aim of the invention is to provide compositions comprising at least one insecticidal active substance of the phenylpyrazole type and which are easily applicable over or into the soil.
  • Another aim of the invention is to provide insecticide compositions whose performance is good in spite of low applicable doses.
  • It has now been found that these aims could be achieved, completely or in part, by means of the compositions and the control method according to the invention which are described in detail below. It is specified that the percentages indicated in the present text are weight/weight percentages, unless otherwise indicated.
  • The subject of the present invention is therefore, firstly, insecticidal compositions comprising:
      • a) between 0.001 and 5%, preferably between 0.05 and 1% and still more advantageously between 0.05 and 0.5% of the compound of formula (I):
        Figure US20050020640A1-20050127-C00001

        in which:
        • R1 is a halogen atom or a CN group or a methyl group or a CH3CO group;
      • R2 is S(O)nR3;
      • R3 is alkyl or haloalkyl;
      • R4 represents a hydrogen or halogen atom, or an NR5R6, S(O)mR7, C(O)R7 or C(O)O—R7, alkyl, haloalkyl or OR8 radical or an —N═C(R9) (R10) radical;
      • R5 and R6 independently represent a hydrogen atom or an alkyl, haloalkyl, C(O)alkyl or S(O)rCF3 radical, or R5 and R6 can together form a divalent alkylene radical which may be interrupted by one or two divalent heteroatoms such as oxygen or sulphur;
        • R7 represents an alkyl or haloalkyl radical;
        • R8 represents an alkyl or haloalkyl radical or a hydrogen atom;
        • R9 represents an alkyl radical or a hydrogen atom;
        • R10 represents a phenyl or heteroaryl group optionally substituted with one or more halogen atoms or groups such as OH, —O-alkyl, —S-alkyl, cyano or alkyl;
        • X represents a trivalent nitrogen atom or a C—R12 radical, the other three valencies of the carbon atom forming part of the aromatic ring;
        • R11 and R12 represent, independently of each other, a hydrogen or halogen atom;
        • R13 represents a halogen atom or a haloalkyl, haloalkoxy, S(O)qCF3 or SF5 group;
        • m, n, q, r represent, independently of each other, an integer equal to 0, 1 or 2;
        • with the proviso that when R1 is methyl, then R3 is haloalkyl, R4 is NH2, R11 is Cl, R13 is CF3 and X is N;
      • b) between 0.05 and 10%, preferably between 0.1 and 5% of one (or more) moisture-retaining agents, preferably a moisture-retaining agent of an organic nature; and
      • c) between 40 and 99%, preferably between 50 and 98% (and more preferably between 70 and 97%) of vegetable meal.
  • The alkyl radicals of the definition of formula (I) generally comprise from 1 to 6 carbon atoms. The ring formed by the divalent alkylene radical representing R5 and R6 as well as by the nitrogen atom to which R5 and R6 are attached is generally a 5-, 6- or 7-membered ring.
  • The compound of formula (I) may be prepared according to one of the methods described in patent applications WO 87/3781, 93/6089, 94/21606, EP 295117 or alternatively by another method within the general knowledge of persons skilled in the art competent in chemical synthesis. This compound is generally designated in the present text by the term active substance.
  • Among the vegetable meals which can be used, there may be mentioned the meals derived from the grinding of cereal grains such as wheat, barley, rye, triticale, oats, or also rice, sorghum, soyabean, maize, the preferred meal being that based on maize. A mixture of these vegetable meals can also be envisaged in the context of the present invention.
  • Among the moisture-retaining agents of an organic nature, there may be mentioned the macromolecular hydrophilic derivatives of plant origin, and in particular the cellulosic hydrophilic derivatives, and more particularly cellulose, but also one or more disintegrating agents. It may be advantageous to use these compounds in particular when meals such as hard wheat meals are used in the granules. Disintegrating agents include: starch, sodium carboxymethyl starch, cellulose such as microcrystalline cellulose; modified celluloses such as sodium carboxymethylcellulose; bentonite, aluminium and magnesium silicate; sodium polynaphthalenesulphonate, sodium dodecylbenzenesulphonate, sodium dioctylsulphosuccinate, lignin sulphonate; a saccharide derivative such as lactose, fructose, sucrose, mannitol, dextrose; a cross-linked derivative of polyvinylpyrrolidone. When a disintegrating agent is used, the composition according to the invention, may contain from 0.5 to 30%, and preferably from 1 to 20%, by weight of the dry substance, of the said agent(s).
  • According to a variant of the composition according to the invention, the composition also comprises from 3 to 30%, preferably from 4 to 20% of sugars. The sugars are chosen in particular from mono-, oligo- or polyorganosaccharides, especially from sucrose, lactose, fructose, dextrose, glucose or alternatively molasses or honey.
  • The compositions which are the subject of the invention may also comprise a preservative preventing the degradation of the meals, such as sodium benzoate, 1,2-benzisothiazolin-3-one, benzoic acid, para-hydroxybenzoic acid and its ester derivatives and its alkali or alkaline-earth metal salts, in particular the sodium salt, 2-phenylphenol and its alkali or alkaline-earth metal salts, in particular the sodium salt, para-nitrophenol.
  • Other additives may also be included such as colourings or attractants for pests or repellents for birds or animals which are useful or which should be protected.
  • Other formulation additives may be used such as binding, agglomerating, appetite-enhancing, agglutinating, gelling, swelling or antiadherent agents and the like.
  • A preferred class of compounds of formula (I) comprises compounds such that R1 is CN, and/or R3 is haloalkyl, and/or R4 is NH2, and/or R11 and R12 are, independently of each other, a halogen atom, and/or R13 is haloalkyl.
  • According to a particularly advantageous variant of the invention, the compound of formula (I) used in the invention is 5-amino-3-cyano-1-[2,6-di-chloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)-sulphinyl]-1H-pyrazole, to which reference is made in the examples under the term “fipronil”.
  • The formulations according to the invention are generally in the form of granules. The size of the granules is advantageously between 0.1 mm and 3 cm, preferably between 0.5 and 4 mm. These granules are advantageously insoluble in water (in the sense that they resist disintegration with water).
  • The compositions according to the invention may be prepared by simply mixing the various constituents, preferably by extrusion or compression in the cold or hot state according to any granulation or pelleting technique known per se. For the production of such granules, reference can be easily made to the European patent application published under the number EP 0575838 and/or to other techniques, for example extrusion techniques, known to persons skilled in the art.
  • The invention also relates to a method of protecting crops from insects, especially click beetles, characterized in that an effective quantity of a composition in the form of granules having a size of between 0.2 mm and 2 cm comprising an active substance chosen from the group consisting of the products of formula I, imidacloprid, acetamiprid, nitenpyram and thiamethoxam, is applied over or into the soil (preferably into the soil) of the area which has to be cultivated.
  • The invention thus relates more particularly to a method of protecting cereal, preferably maize or beet or sunflower or potato or rape, crops. The application of the formulations according to the invention takes place advantageously before sowing the said crop, or simultaneously with this sowing.
  • The invention also relates to a method of controlling insects, especially click beetles, characterized in that an effective quantity of one of the compositions according to the invention is applied over or into the soil (preferably into the soil) where they are present or are likely to be present.
  • As effective quantity, quantities of composition corresponding to a dose of compound of formula (I) of between 1 and 50 g/ha, preferably between 3 and 40 g/ha are often used.
  • A specific characteristic of the method of controlling insects according to the invention consists in the application, over or into the soil, of a composition providing a dose which is nonlethal through contact but lethal through ingestion.
  • In other words, in the specific case of click beetles, the method consists in killing the click beetles by application of a dose which is nonlethal through contact but lethal through ingestion. A hypothesis for the good efficacy of the method of treatment according to the invention, which makes it possible to greatly reduce the applicable doses of compounds of formula I in particular, is based on the fact that once the bait according to the invention has caused the death of a click beetle, the latter can itself serve as bait for other click beetles, which therefore also ingest a product (dead click beetle) containing the insecticide.
  • For the purposes of the present text, the words insecticide and insect should be taken in their broad ordinary sense and not in their strictly scientific (zoological) sense. Accordingly, the term insect is understood to mean any animal of a very small size such as arthropods (insects in the strict and zoological sense, arachnids, myriapods) and nematodes.
  • As soil insects against which the invention is particularly effective, there may be mentioned for example:
  • The Coleoptera (wireworms (Agriotes spp.), false wireworms, white grubs) such as for example:
  • Agriotes lineatus (European click beetle, Elateridae),
  • Agriotes sordidus (European click beetle, Elateridae),
  • Agriotes obscurus (European click beetle, Elateridae),
  • Agriotes sputator (European click beetle, Elateridae),
  • Athous spp. (Elateridae),
  • Atomaria linearis (Cryptophagidae)
  • Melolontha spp. (white grubs, Scarabaeidae),
  • Bothynoderes
  • Limonius spp. (US click beetle),
  • Melanotus spp. (US click beetle),
  • Diabrotica spp. (cornrootworms, Crysomelidae),
  • Tanymecus pallidus (beet leaf weevil, Curculionidae).
  • The Lepidoptera (Noctuidae) such as:
  • Autographa spp., Mamestra spp., Agrotis spp. (cutworms, grey grubs), Euxoa spp. (cutworms, grey grubs), Spodoptera spp. (Spodoptera exigua, Spodoptera littorlis). A
  • The Diptera such as Tipula spp.).
  • The Myriapoda (Myriapoda):
      • Diplopoda=Millipedes,
      • Centipede.
  • Among the soil click beetles against which the invention is particularly effective, there may be mentioned Agriotes spp., Athous spp., Limonius spp.
  • The granules according to the invention are advantageously inserted into the soil at a depth of between 1 and 5 cm.
  • The compositions according to the invention are particularly advantageous in that they allow the use of lower doses of active product than similar known compositions.
  • The following examples illustrate the invention without however constituting a limitation thereto. In these examples, the compound of formula (I) used is fipronil.
  • EXAMPLE 1
  • A surface of 0.1 ha is sown with maize at the rate of about 8000 untreated seeds. This surface is divided into 40-m2 plots.
  • At the same time as the sowing, there are incorporated into the soil, in the sowing row, 2 mm granules containing a composition consisting of:
  • 0.25% of fipronil,
  • 93.5% of maize meal,
  • 2% of cellulose,
  • 4% of lactose,
  • 0.2% of para-nitrophenol,
  • 0.05% of pigment blue 15.3.
  • The quantities of granules thus spread vary from 2.5 to 10 kg per hectare. Untreated plots are kept to serve as control and to verify the extent of the damage by the insects. Likewise, the plots will be treated with a commercial insecticide which is reputed effective and called reference. Each modality is repeated four times.
  • Approximately 20 days after sowing, the maize plants which have emerged are counted.
  • In the locality of St Hilaire (30), 22 days after sowing, 19 plants are observed in the furrow of the 4 untreated plots per 10 metres of furrow. In the plots treated according to the invention with the dose of fipronil of 6 g per hectare, 49 plants are observed per 10 metres of furrow.
  • With the dose of fipronil of 12.5 g per hectare, 48 to 50.5 plants are observed per 10 metres of furrow.
  • With the dose of fipronil of 25 g per hectare, 45.5 to 51.3 plants are observed per 10 metres of furrow.
  • With the dose of fipronil of 50 g per hectare, 49 plants are observed per 10 metres of furrow.
  • To obtain the same result with a conventional granule (clay carrier), 200 g of fipronil have to be provided per hectare.
  • The soil is dug out and scraped in order to capture and identify the insects responsible for the damage; a large presence of larvae of click beetles of the genus Agriotes, in particular Agriotes sordidus, is observed for the untreated control.
  • EXAMPLE 2
  • A surface of 1 ha is sown with maize at the rate of about 98,100 untreated seeds. This surface is divided into 27-m2 plots.
  • At the same time as the sowing, there are incorporated into the soil, in the sowing row, 2 mm granules containing a composition consisting of:
  • 0.25% of fipronil,
  • 93.5% of maize meal
  • 2% of cellulose,
  • 4% of lactose,
  • 0.2% of para-nitrophenol,
  • 0.05% of pigment blue 15.3.
  • The quantities of granules thus spread vary from 2.5 to 10 kg per hectare. Untreated plots are kept to serve as control and to verify the extent of the damage by the insects. Likewise, the plots will be treated with a commercial insecticide which is reputed effective and called reference. Each modality is repeated four times.
  • Approximately 50 days after sowing, the maize plants which have emerged are counted.
  • In the locality of Beaufort (62), 50 days after sowing, 30 plants are observed in the furrow of the 4 untreated plots per 10 metres of furrow. In the plots treated according to the invention with the dose of fipronil of 6 g per hectare, 40 plants are observed per 10 metres of furrow.
  • With the dose of fipronil of 12.5 g per hectare, 43 to 46 plants are observed per 10 metres of furrow.
  • With the dose of fipronil of 25 g per hectare, 44.5 to 50 plants are observed per 10 metres of furrow.
  • With the dose of fipronil of 50 g per hectare, 49.8 plants are observed per 10 metres of furrow.
  • To obtain the same result (52 plants per 10 metres) with a conventional granule (clay carrier), 200 g of fipronil have to be provided per hectare.
  • The soil is dug out and scraped in order to capture and identify the insects responsible for the damage; a large presence of larvae of click beetles of the genus Agriotes, in particular Agriotes lineatus.
  • EXAMPLE 3
  • Test of efficacy of the bait granules according to the invention on potato crop.
  • At the same time as the sowing, there are incorporated into the soil, in the sowing row, granules according to the invention consisting of.:
  • 12.5 g/kg of fipronil (from an SC containing 500 g/l of fipronil),
  • 945.5 g/kg of a) maize meal (granules A) or b) rice meal (granules B),
  • 40 g/kg of lactose,
  • 2 g/kg of para-nitrophenol.
  • The efficacy against Agriotes (click beetles), 90 days after sowing, of the two granules A and B above, used at the doses of 5 and 2.5 g of fipronil per hectare, and of the same fipronil used by spraying at the doses of 50 and 25 g/ha (from Regent® 800WG) (compound C), was compared.
  • The following results, expressed as number of holes per 10 tubers (═N) are then observed:
    Product A A B B C C Control*
    Dose (g · ha) 2.5 5 2.5 5 25 50
    N 6 1 7 3 6 1 14

    *untreated control.
  • This result indeed shows the good control of click beetles which is obtained by the granules according to the invention which give the same result as Regent® 800WG but with a dose reduced by a factor of 10.

Claims (17)

1. Insecticidal compositions comprising:
a) between 0.001 and 5%, preferably between 0.05 and 1% and still more advantageously between 0.05 and 0.5% of a compound of formula (I):
Figure US20050020640A1-20050127-C00002
in which:
R1 is a halogen atom or a CN group or a methyl group or a CH3CO group;
R2 is S(O)nR3;
R3 is alkyl or haloalkyl;
R4 represents a hydrogen or halogen atom, or an NR5R6, S(O)mR7, C(O)R7 or C(O)O—R7, alkyl, haloalkyl or OR8 radical or an —N═C(R9) (R10) radical;
R5 and R6 independently represent a hydrogen atom or an alkyl, haloalkyl, C(O)alkyl or S(O)rCF3 radical, or R5 and R6 can together form a divalent alkylene radical which may be interrupted by one or two divalent heteroatoms such as oxygen or sulphur;
R7 represents an alkyl or haloalkyl radical;
R8 represents an alkyl or haloalkyl radical or a hydrogen atom;
R9 represents an alkyl radical or a hydrogen atom;
R10 represents a phenyl or heteroaryl group optionally substituted with one or more halogen atoms or groups such as OH, —O-alkyl, —S-alkyl, cyano or alkyl;
R11 and R12 represent, independently of each other, a hydrogen or halogen atom;
R13 represents a halogen atom or a haloalkyl, haloalkoxy, S(O)qCF3 or SF5 group;
m, n, q, r represent, independently of each other, an integer equal to 0, 1 or 2;
with the proviso that when R1 is methyl, then R3 is haloalkyl, R4 is NH2, R11 is Cl, R13 is CF3 and X is N;
b) between 0.05 and 10%, preferably between 0.1 and 5% of one (or more) moisture-retaining agents, preferably a moisture-retaining agent of an organic nature; and
c) between 40 and 99%, preferably between 50 and 98% (and more preferably between 70 and 97%) of vegetable meal.
2. Insecticidal compositions according to claim 1, characterized in that the meals are derived from the grinding of cereal grains such as wheat, barley, rye, triticale, oats, or also rice, sorghum, soyabean, maize.
3. Insecticidal compositions according to either of claims 1 and 2, characterized in that the meal is a maize meal.
4. Insecticidal compositions according to one of claims 1 to 3, characterized in that among the moisture-retaining agents of an organic nature, there may be mentioned macromolecular hydrophilic derivatives of plant origin, and in particular cellulosic hydrophilic derivatives, and more particularly cellulose.
5. Insecticidal compositions according to one of claims 1 to 4, characterized in that the composition also comprises from 3 to 30%, preferably from 4 to 20% of sugars.
6. Insecticidal compositions according to one of claims 1 to 4, characterized in that the sugars are chosen in particular from mono-, oligo- or polyorganosaccharides, especially from sucrose, lactose, fructose, dextrose, glucose or alternatively molasses or honey.
7. Insecticidal compositions according to one of claims 1 to 6, characterized in that they also comprise a preservative preventing the degradation of the meals, chosen from sodium benzoate, 1,2-benzisothiazolin-3-one, benzoic acid, para-hydroxybenzoic acid and its ester derivatives and its alkali or alkaline-earth metal salts, in particular the sodium salt, 2-phenylphenol and its alkali or alkaline-earth metal salts, in particular the sodium salt, para-nitrophenol.
8. Insecticidal compositions according to one of claims 1 to 7, characterized in that they comprise other additives such as colourings or attractants for pests or repellants for birds or animals which are useful or which should be protected, and/or other formulation additives such as binding, agglomerating, appetite-enhancing, agglutinating, gelling, swelling and antiadherent agents and the like.
9. Insecticidal compositions according to one of claims 1 to 8, characterized in that the compound of formula (I) is 5-amino-3-cyano-1-[2,6-di-chloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)-sulphinyl]-1H-pyrazole.
10. Insecticidal compositions according to one of claims 1 to 9, characterized in that the formulations according to the invention are in the form of granules, the size of these granules being advantageously between 0.1 mm and 3 cm, preferably between 0.5 and 4 mm and in that these granules are advantageously insoluble in water.
11. Method of controlling insects, characterized in that an effective quantity of a composition according to one of claims 1 to 10 in the form of granules having a size of between 0.2 mm and 2 cm is applied over or into the soil (preferably into the soil) of the area which has to be cultivated.
12. Method of protecting crops according to claim 11, characterized in that a compound of formula I is used.
13. Method according to either of claims 11 and 12, characterized in that cereal, preferably maize or beet or sunflower or potato or rape, crops are protected.
14. Method according to one of claims 11 to 13, characterized in that an effective quantity of one of the compositions according to the invention is used for controlling insects, especially click beetles.
15. Method according to one of claims 12 to 14, characterized in that the effective quantity of composition corresponds to a dose of compound of formula (I) of between 1 and 50 g/ha, preferably between 3 and 40 g/ha.
16. Method of controlling insects which consists in the application, over or into the soil, of a composition providing a dose which is nonlethal through contact but lethal through ingestion.
17. Method according to claim 16, applicable to click beetles.
US10/893,902 1999-09-07 2004-07-20 Method of controlling soil insects with phenylpyrazoles Abandoned US20050020640A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US10/893,902 US20050020640A1 (en) 1999-09-07 2004-07-20 Method of controlling soil insects with phenylpyrazoles

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
FR99/11312 1999-09-07
FR9911312A FR2798042B1 (en) 1999-09-07 1999-09-07 INSECTICIDE COMPOSITIONS HAVING PHENYL-PYRAZOLE TYPE ACTIVE MATERIAL AND METHOD FOR CONTROLLING SOIL INSECTS
US10/070,457 US6939830B1 (en) 1999-09-07 2000-09-07 Method for fighting soil insects with phenyl-pyrazoles
US10/893,902 US20050020640A1 (en) 1999-09-07 2004-07-20 Method of controlling soil insects with phenylpyrazoles

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
PCT/FR2000/002460 Division WO2001017354A1 (en) 1999-09-07 2000-09-07 Method for fighting soil insects with phenyl-pyrazoles
US10/070,457 Division US6939830B1 (en) 1999-09-07 2000-09-07 Method for fighting soil insects with phenyl-pyrazoles

Publications (1)

Publication Number Publication Date
US20050020640A1 true US20050020640A1 (en) 2005-01-27

Family

ID=9549692

Family Applications (2)

Application Number Title Priority Date Filing Date
US10/070,457 Expired - Lifetime US6939830B1 (en) 1999-09-07 2000-09-07 Method for fighting soil insects with phenyl-pyrazoles
US10/893,902 Abandoned US20050020640A1 (en) 1999-09-07 2004-07-20 Method of controlling soil insects with phenylpyrazoles

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US10/070,457 Expired - Lifetime US6939830B1 (en) 1999-09-07 2000-09-07 Method for fighting soil insects with phenyl-pyrazoles

Country Status (32)

Country Link
US (2) US6939830B1 (en)
EP (1) EP1209976B1 (en)
CN (1) CN1372439A (en)
AR (1) AR025596A1 (en)
AT (1) ATE243421T1 (en)
AU (1) AU770778B2 (en)
BG (1) BG65082B1 (en)
BR (1) BR0013800B1 (en)
CA (1) CA2383087A1 (en)
CO (1) CO5221065A1 (en)
CZ (1) CZ294602B6 (en)
DE (1) DE60003567T2 (en)
DK (1) DK1209976T3 (en)
EA (1) EA004313B1 (en)
EG (1) EG22538A (en)
ES (1) ES2195934T3 (en)
FR (1) FR2798042B1 (en)
HR (1) HRP20020277B1 (en)
HU (1) HU226075B1 (en)
IL (2) IL148162A0 (en)
MA (1) MA25500A1 (en)
MX (1) MXPA02002352A (en)
MY (1) MY122764A (en)
NZ (1) NZ517450A (en)
PE (1) PE20010477A1 (en)
PL (1) PL200934B1 (en)
PT (1) PT1209976E (en)
SK (1) SK286692B6 (en)
TW (1) TWI239234B (en)
UA (1) UA73527C2 (en)
WO (1) WO2001017354A1 (en)
ZA (1) ZA200201562B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010022917A2 (en) * 2008-08-27 2010-03-04 Bayer Cropscience Ag Method of controlling soul insects
FR2993432A1 (en) * 2012-07-20 2014-01-24 Sumitomo Chemical Co METHOD FOR REDUCING DAMAGE IN MAIZE CROPS FROM HARMFUL ORGANISMS

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0211924D0 (en) * 2002-05-23 2002-07-03 Syngenta Ltd Composition
US7281367B2 (en) * 2003-12-05 2007-10-16 Alliant Techsystems Inc. Steerable, intermittently operable rocket propulsion system
WO2005094578A1 (en) 2004-03-29 2005-10-13 Dow Agrosciences Llc Pesticide compositions
FR2932954B1 (en) * 2008-06-25 2010-11-05 Sbm Dev METHOD FOR CONTROLLING SOIL INSECTS
KR20110099257A (en) 2008-11-25 2011-09-07 바스프 에스이 Multipurpose ant bait
EP2446742A1 (en) 2010-10-28 2012-05-02 Bayer CropScience AG Insecticide or acaricide compositions containing mono- or disaccharides as activity enhancers
FR2979185B1 (en) * 2011-08-25 2015-07-31 Sbm Dev METHOD FOR CONTROLLING SOIL INSECTS
FR2979186B1 (en) * 2011-08-25 2015-01-16 Sbm Dev METHOD FOR CONTROLLING SOIL INSECTS
CN105685061A (en) * 2016-02-29 2016-06-22 陕西西大华特科技实业有限公司 Application of benziothiazolinone in preventing and treating potato seed-borne diseases and promoting rooting and germination

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4834977A (en) * 1987-03-06 1989-05-30 Sumitomo Chemical Company, Limited Poison bait for control of noxious insects
US5232940A (en) * 1985-12-20 1993-08-03 Hatton Leslie R Derivatives of N-phenylpyrazoles
US5567429A (en) * 1993-12-21 1996-10-22 Sumitomo Chemical Company, Limited Pest controlling composition
US5580843A (en) * 1993-12-22 1996-12-03 Bayer Aktiengesellschaft Substituted 1-arylpyrazoles
US5849320A (en) * 1996-06-13 1998-12-15 Novartis Corporation Insecticidal seed coating
US5939441A (en) * 1994-04-25 1999-08-17 Bayer Aktiengesellschaft Substituted pyridylpyrazoles

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5762201A (en) * 1980-09-30 1982-04-15 Sumitomo Chem Co Ltd Bait composition for controlling insect rest
GB8713768D0 (en) * 1987-06-12 1987-07-15 May & Baker Ltd Compositions of matter
GB8531485D0 (en) 1985-12-20 1986-02-05 May & Baker Ltd Compositions of matter
JP2585319B2 (en) * 1987-11-30 1997-02-26 住友化学工業株式会社 Poison bait for pest control
GB9120641D0 (en) 1991-09-27 1991-11-06 Ici Plc Heterocyclic compounds
GB9306184D0 (en) 1993-03-25 1993-05-19 Zeneca Ltd Heteroaromatic compounds
JPH08175910A (en) * 1994-12-19 1996-07-09 Sumitomo Chem Co Ltd Poison bait agent for ant
FR2735950B1 (en) 1995-06-29 1997-08-01 Rhone Poulenc Agrochimie INSECTICIDE COMPOSITIONS BASED ON A PHENYLPYRAZOLE DERIVATIVE, IN PARTICULAR FOR FIGHTING ANTS
FR2737085B1 (en) * 1995-07-26 1997-08-22 Rhone Poulenc Agrochimie INSECTICIDE ASSOCIATIONS OF A CARBAMATE OXIME WITH A PYRAZOLE OR PHENYLIMIDAZOLE GROUP INSECTICIDE

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5232940A (en) * 1985-12-20 1993-08-03 Hatton Leslie R Derivatives of N-phenylpyrazoles
US4834977A (en) * 1987-03-06 1989-05-30 Sumitomo Chemical Company, Limited Poison bait for control of noxious insects
US5567429A (en) * 1993-12-21 1996-10-22 Sumitomo Chemical Company, Limited Pest controlling composition
US5580843A (en) * 1993-12-22 1996-12-03 Bayer Aktiengesellschaft Substituted 1-arylpyrazoles
US5939441A (en) * 1994-04-25 1999-08-17 Bayer Aktiengesellschaft Substituted pyridylpyrazoles
US5849320A (en) * 1996-06-13 1998-12-15 Novartis Corporation Insecticidal seed coating

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010022917A2 (en) * 2008-08-27 2010-03-04 Bayer Cropscience Ag Method of controlling soul insects
WO2010022917A3 (en) * 2008-08-27 2011-06-23 Bayer Cropscience Ag Method of controlling soil insects
FR2993432A1 (en) * 2012-07-20 2014-01-24 Sumitomo Chemical Co METHOD FOR REDUCING DAMAGE IN MAIZE CROPS FROM HARMFUL ORGANISMS
US9265189B2 (en) 2012-07-20 2016-02-23 Sumitomo Chemical Company, Limited Method for reducing damage by harmful organisms in corn cultivation

Also Published As

Publication number Publication date
IL148162A (en) 2007-06-03
EG22538A (en) 2003-03-31
ES2195934T3 (en) 2003-12-16
EA200200340A1 (en) 2002-10-31
SK3252002A3 (en) 2002-07-02
HRP20020277B1 (en) 2007-09-30
MXPA02002352A (en) 2002-08-12
CZ2002819A3 (en) 2002-06-12
WO2001017354A1 (en) 2001-03-15
CO5221065A1 (en) 2002-11-28
TWI239234B (en) 2005-09-11
MY122764A (en) 2006-05-31
HUP0202802A3 (en) 2005-03-29
PL200934B1 (en) 2009-02-27
UA73527C2 (en) 2005-08-15
ZA200201562B (en) 2003-07-30
PE20010477A1 (en) 2001-04-17
CA2383087A1 (en) 2001-03-15
FR2798042B1 (en) 2003-04-25
HRP20020277A2 (en) 2003-06-30
MA25500A1 (en) 2002-07-01
BG65082B1 (en) 2007-02-28
CN1372439A (en) 2002-10-02
SK286692B6 (en) 2009-03-05
EA004313B1 (en) 2004-02-26
DK1209976T3 (en) 2003-08-18
HUP0202802A2 (en) 2002-12-28
CZ294602B6 (en) 2005-02-16
BG106449A (en) 2002-09-30
HU226075B1 (en) 2008-04-28
DE60003567T2 (en) 2004-04-29
US6939830B1 (en) 2005-09-06
FR2798042A1 (en) 2001-03-09
BR0013800A (en) 2002-05-21
PL355561A1 (en) 2004-05-04
NZ517450A (en) 2004-05-28
BR0013800B1 (en) 2013-06-18
AU770778B2 (en) 2004-03-04
AU7299000A (en) 2001-04-10
EP1209976B1 (en) 2003-06-25
DE60003567D1 (en) 2003-07-31
AR025596A1 (en) 2002-12-04
EP1209976A1 (en) 2002-06-05
PT1209976E (en) 2003-10-31
ATE243421T1 (en) 2003-07-15
IL148162A0 (en) 2002-09-12

Similar Documents

Publication Publication Date Title
CA2239081C (en) Novel 5-amino-3-cyano-4-ethylsulfinyl-1-phenyl-pyrazole compounds and their use as pesticides
US20090203746A1 (en) Synergistic Insecticidal Composition Containing Chloronicotynyle and Pyrethroids Compounds
US6939830B1 (en) Method for fighting soil insects with phenyl-pyrazoles
NZ586507A (en) Composition of phenylsemicarbazones for protecting a plant that grows from the treated seed against a pest
US20060177474A1 (en) Agricultural and horticultural poison bait preparation
EA002283B1 (en) Pesticidal 1-arylpyrazoles
JP4742333B2 (en) N-thiadiazolylcyclopropanecarboxylic acid amides and insecticides and acaricides containing the same as active ingredients
JP4640538B2 (en) Pyridazinones and pest control agents containing the same as active ingredients
TH27700B (en) Insecticidal mixtures containing the active ingredient of phenylpirazole. And how to control soil insects
TH48791A (en) Insecticidal mixtures containing the active ingredient of phenylpirazole. And how to control soil insects
JP2004292411A (en) Ingestion-type pesticide composition having water resistance

Legal Events

Date Code Title Description
AS Assignment

Owner name: BASF AGRO B.V., ARNHEM (NL), WADENSWIL-BRANCH, SWI

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:AVENTIS CROPSCIENCE SA;REEL/FRAME:015811/0001

Effective date: 20041216

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION