EP2164323A1 - Mélanges comprenant du 1-méthylcyclopropène - Google Patents

Mélanges comprenant du 1-méthylcyclopropène

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Publication number
EP2164323A1
EP2164323A1 EP07857421A EP07857421A EP2164323A1 EP 2164323 A1 EP2164323 A1 EP 2164323A1 EP 07857421 A EP07857421 A EP 07857421A EP 07857421 A EP07857421 A EP 07857421A EP 2164323 A1 EP2164323 A1 EP 2164323A1
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EP
European Patent Office
Prior art keywords
methyl
plant
inhibitors
component
acid
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.)
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Application number
EP07857421A
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German (de)
English (en)
Inventor
Annette Freund
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.)
Rohm and Haas Co
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Rohm and Haas Co
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Filing date
Publication date
Application filed by Rohm and Haas Co filed Critical Rohm and Haas Co
Priority to EP10176165A priority Critical patent/EP2258177A3/fr
Priority to EP07857421A priority patent/EP2164323A1/fr
Publication of EP2164323A1 publication Critical patent/EP2164323A1/fr
Withdrawn legal-status Critical Current

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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
    • A01N27/00—Biocides, pest repellants or attractants, or plant growth regulators containing hydrocarbons

Definitions

  • the present invention relates to agrochemical mixtures, comprising 1-methylcyclopropene as component (A) and as component (B) at least one active compound selected from the active ingredients as defined below, and to a method for improving the yield, the plant health and/or the vigor of an agricultural plant by applying to the plant, the locus where the plant is growing or is expected to grow, and/or the seeds from which the plant grows a non-phytotoxic effective amount of component (A) and as component (B) at least one active compound selected from the active ingredients as defined below.
  • a problem underlying the present invention is the desire for compositions that improve plants, a process which is commonly and hereinafter referred to as "plant health”.
  • Another problem of the present invention is the need to manage plant stress, such as drought stress, cold stress, heat stress, salt stress or UV stress and all other biotic and abiotic stresses especially to reduce plant stress responses such as premature leaf senescence, undesired defoliation, reduced plant growth, reduced plant yield, abortion of flowers and fruits, and also stress responses due to plant pathogens or pest pressure.
  • plant stress such as drought stress, cold stress, heat stress, salt stress or UV stress and all other biotic and abiotic stresses especially to reduce plant stress responses such as premature leaf senescence, undesired defoliation, reduced plant growth, reduced plant yield, abortion of flowers and fruits, and also stress responses due to plant pathogens or pest pressure.
  • Another problem of the present invention is the desire for reducing unfavourable responses of plants associated with the treatment of undesired weeds with herbicides.
  • the present invention provides an agrochemical mixture, comprising as component (A) 1-methylcyclopropene and as component (B) at least one active compound selected from the group consisting of B1 ) famoxadone (5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-2,4- oxazolidinedione); B2) carboxylic amides selected from benalaxyl, benodanil, boscalid, carboxin, mepronil, fenfuram, fenhexamid, flutolanil, furametpyr, metalaxyl, ofurace, oxadixyl, oxycarboxin, penthiopyrad, thifluzamid, tiadinil, 4-difluoromethyl-2- methyl-thiazol-5-carboxylic acid
  • organophosphorous compounds selected from edifenphos, fosetyl, fosetyl- aluminium, iprobenfos, pyrazophos, tolclofos-methyl, phosphoric acid and the salts thereof;
  • B1 1 organo-chloro compounds selected from thiophanate methyl, chlorothalonil, dichlofluanid, tolylfluanid, flusulfamid, phthalide, hexachlorbenzene, pencycuron, quintozen;
  • B12 nitrophenyl derivatives selected from binapacryl, dinocap and dinobuton;
  • organo(thio)phosphates selected from acephate, azamethiphos, azinphos- methyl, chlorpyrifos, chlorpyrifos-methyl, chlorfenvinphos, diazinon, dichlorvos, dicrotophos, dimethoate, disulfoton, ethion, fenitrothion, fenthion, isoxathion, malathion, methamidophos, methidathion, methyl-parathion, mevinphos, mo- nocrotophos, oxydemeton-methyl, paraoxon, parathion, phenthoate, phosalone, phosmet, phosphamidon, phorate, phoxim, pirimiphos-methyl, profenofos, prothiofos, sulprophos, tetrachlorvinphos, terbufos, triazophos and trichlorfon; B19) carba
  • B21 growth regulators selected from a) chitin synthesis inhibitors that are selected from the benzoylureas chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, teflubenzuron, triflumuron; bu- profezin, diofenolan, hexythiazox, etoxazole and clofentazine; b) ecdysone antagonists that are selceted from halofenozide, methoxyfenozide, tebufenozide and azadirachtin; c) juvenoids that are selected from pyriproxyfen, methoprene and fenoxycarb and d) lipid biosynthesis inhibitors that are selected from spirodi- clofen, spiromesifen and spirotetramat; B22) nicot
  • GABA antagonist compounds selected from acetoprole, endosulfan, ethi- prole, 5-amino-1 -(2,6-dichloro- ⁇ , ⁇ , ⁇ -trifluoro-p-tolyl)-4- trifluoromethylsulfinylpyrazole-3-carbonitrile (fipronil), vaniliprole, pyrafluprole, pyriprole and the phenylpyrazole compound of formula F 2
  • METI I compounds selected from fenazaquin, pyridaben, tebufenpyrad, tolf- enpyrad and flufenerim;
  • METI Il and III compounds selected from acequinocyl, fluacyprim and hy- dramethylnon;
  • B28 oxidative phosphorylation inhibitor compounds selected from cyhexatin, diafenthiuron, fenbutatin oxide and propargite;
  • B32 a compound selected from benclothiaz, bifenazate, cartap, flonicamid, pyri- dalyl, pymetrozine, sulfur, thiocyclam, flubendiamide, cyenopyrafen, flupyrazofos, cyflumetofen, amidoflumet, the aminoquinazolinone compound of formula F 4
  • a 1 is CH 3 , Cl, Br, I
  • X is C-H, C-Cl, C-F or N
  • Y' is F, Cl, or Br
  • Y" is F, Cl, CF 3
  • B 1 is hydrogen, Cl, Br, I, CN
  • B 2 is Cl, Br, CF 3 , OCH 2 CF 3 , OCF 2 H
  • R B is hydrogen, CH 3 or CH(CHs) 2 ;
  • lipid biosynthesis inhibitors selected from chlorazifop, clodinafop, clofop, cyhalofop, diclofop, fenoxaprop, fenoxaprop-p, fenthiaprop, fluazifop, fluazifop-P, haloxyfop, haloxyfop-P, isoxapyrifop, metamifop, propaquizafop, quizalofop, qui- zalofop-P, trifop, alloxydim, butroxydim, clethodim, cloproxydim, cycloxydim, pro- foxydim, sethoxydim, tepraloxydim, tralkoxydim, butylate, cycloate, diallate, di- mepiperate, EPTC, esprocarb, ethiolate, isopolinate, methiobencarb,
  • protoporphyrinogen-IX oxidase inhibitors selected from acifluorfen, bifenox, chlomethoxyfen, chlornitrofen, ethoxyfen, fluorodifen, fluoroglycofen, fluoronitro- fen, fomesafen, furyloxyfen, halosafen, lactofen, nitrofen, nitrofluorfen, oxyfluor- fen, fluazolate, pyraflufen, cinidon-ethyl, flumiclorac, flumioxazin, flumipropyn, flu- thiacet, thidiazimin, oxadiazon, oxadiargyl, azafenidin, carfentrazone, sulfentra- zone, pentoxazone, benzfendizone, butafenacil, pyraclonil, profluazol, flufenpyr, flupropacil,
  • B38 glyphosate in its acid form or as a derivative thereof, such as the mono iso- propylammonium salt, the sodium salt, trimesium salt (sulfosate) or a mixture thereof;
  • mitose inhibitors selected from benfluralin, butralin, dinitramine, ethalflu- ralin, fluchloralin, isopropalin, methalpropalin, nitralin, oryzalin, pendimethalin, prodiamine, profluralin, trifluralin, amiprofos-methyl, butamifos, dithiopyr, thia- zopyr, propyzamide, tebutam, chlorthal, carbetamide, chlorbufam, chlorpropham and propham;
  • VLCFA inhibitors selected from acetochlor, alachlor, butachlor, butenachlor, delachlor, diethatyl, dimethachlor, dimethenamid, dimethenamid-P, metazachlor, metolachlor, S-metolachlor, pretilachlor, propachlor, propisochlor, prynachlor, terbuchlor, thenylchlor, xylachlor, allidochlor, CDEA, epronaz, diphenamid, napropamide, naproanilide, pethoxamid, flufenacet, mefenacet, fentrazamide, anilofos, piperophos, cafenstrole, indanofan and tridiphane; B43) cellulose biosynthesis inhibitors selected from dichlobenil, chlorthiamid, isoxaben and flupoxam;
  • B44 decoupler herbicides selected from dinofenate, dinoprop, dinosam, dinoseb, dinoterb, DNOC, etinofen and medinoterb;
  • B45 auxin herbicides selected from clomeprop, 2,4-D, 2,4,5-T, MCPA, MCPA thioethyl, dichlorprop, dichlorprop-P, mecoprop, mecoprop-P, 2,4-DB, MCPB, chloramben, dicamba, 2,3,6-TBA, tricamba, clopyralid, fluroxypyr, picloram, tri- clopyr, benazolin, aminopyralid, quinclorac, and quinmerac;
  • B46 auxin transport inhibitors selected from naptalam and diflufenzopyr;
  • B47 benzoylprop, flamprop, flamprop-M, bromobutide, chlorflurenol, cinmethylin, methyldymron, eto
  • mixtures are being applied comprising the component (A) and one component (B), however, mixtures may also comprise the component (A) as well as one or more components (B) such as one, two or three of the active compounds selected from the groups B1 to B50.
  • 1-methylcyclopropene is a well-known plant growth regulator and ethylene-binding inhibitor which prevents the signal from ethylene to initiate stress responses in plants and which inhibits the sensitivity of plants or plant parts (e.g. fruits and flowers) to ethylene by inhibiting its perception. Consequently, certain processes like the ripening in fruits are slowed down.
  • Ethylene has been shown to be involved in various kinds of plant stress. Increased levels of ethylene in plants are for example responsible for many deleterious effects such as early senescence, fruit deterioration and inhibition of root elongation.
  • 1-methylcyclopropene is used as an ethylene antagonist for re- ducing stress induction and prolonging the life of ornamental plants and cut flowers by preventing ethylene from attaching to plant tissues. It is a postharvest tool for counteracting undesirable effects of ethylene on harvested fruits and vegetables during transport and storage as ethylene also promotes ripening and aging of plants, flowers, fruits, and vegetables.
  • the active compounds of groups B1 ) to B50) that can be used as component (B), their preparation and their action against harmful fungi, pests and undesirable weeds are generally known; they are commercially available. In most of the cases, they can also be found in The Pesticide Manual, 13 th Edition, British Crop Protection Council (2003) among other publications.
  • bromuconazole 1-[[4-bromo-2-(2,4-dichlorophenyl)tetrahydro-2-furanyl]methyl]-1 H- 1 ,2,4-triazole (Proc. 1990 Br. Crop. Prot. Conf. - Pests Dis. Vol. 1 , p. 459); - cyproconazole, 2-(4-chlorophenyl)-3-cyclopropyl-1 -[1 ,2,4]triazol-1 -ylbutan-2-ol (US 4 664 696);
  • aldimorph 4-alkyl-2,5(or 2,6)-dimethylmorpholine, comprising 65-75% of 2,6- dimethylmorpholine and 25-35% of 2,5-dimethylmorpholine, comprising more than 85% of 4-dodecyl-2,5(or 2,6)-dimethylmorpholine, where "alkyl” may also include octyl, de- cyl, tetradecyl or hexadecyl and where the cis/trans ratio is 1 :1 ;
  • Thiamides of formula r 1 and their preparation have been described in WO 98/28279. Lepimection is known from Agro Project, PJB Publications Ltd, November 2004. Ben- clothiaz and its preparation have been described in EP-A1 454621. Methidathion and Paraoxon and their preparation have been described in Farm Chemicals Handbook, Volume 88, Meister Publishing Company, 2001. Acetoprole and its preparation have been described in WO 98/28277. Flupyrazofos has been described in Pesticide Science 54, 1988, p.237-243 and in US 4822779. Pyrafluprole and its preparation have been described in JP 2002193709 and in WO 01/00614.
  • component (B) is famoxadone.
  • component (B) is a carbox- ylic amide selected from the group B2).
  • component (B) is an azole selected from the group B3).
  • component (B) is a nitrogen-containing heterocyclic compound selected from the group B4).
  • component (B) is a car- bamate or thiocarbamate selected from the group B5).
  • component (B) is a gua- nidine selected from the group B6).
  • component (B) is an antibiotic selected from the group B7). According to another embodiment of the present invention, component (B) is a fentin salt.
  • component (B) is iso- prothiolan or dithianon.
  • component (B) is an organophosphorous compound selected from the group B10).
  • component (B) is an or- gano-chloro compound selected from the group B11 ).
  • component (B) is a nitro- phenyl derivative selected from the group B12).
  • component (B) is an inorganic ingredient selected from the group B13).
  • component (B) is an ALS inhibitor selected from the group B34).
  • component (B) is clothianidin.
  • component (B) is glufosinat.
  • component (B) is spiroxam- ine.
  • component (B) is cy- flufenamide.
  • component (B) is cymox- anil.
  • component (B) is metrafenone.
  • component (B) is (EZ)-3-(2-chloro-1 ,3-thiazol-5-ylmethyl)-5-methyl-1 ,3,5-oxadiazinan-4- ylidene(nitro)amine (thiamethoxam).
  • component (B) is 5-amino-1-(2,6-dichloro- ⁇ , ⁇ , ⁇ -trifluoro-p-tolyl)-4-trifluoromethylsulfinylpyrazole-3- carbonitrile (fipronil).
  • component (B) is(EZ)-1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine (imidacloprid).
  • component (B) is prohexadione-Ca.
  • component (B) is glyphosate.
  • component (B) is diflufenzopyr.
  • compositions are suitable for improving the health of plants when applied to plants, parts of plants, seeds, or at their locus of growth.
  • 1-methylcyclopropene can be used as synergist for a variety of different active ingredients.
  • a component (B) By simultaneous application of the 1-methylcyclopropene with a component (B) together or by separate application of 1-methylcyclopropene and component (B), said effects are increased more than additively.
  • 1- methylcyclopropene and component (B) are thus preferably present in synergistic amounts.
  • the present invention provides the use of a composition as defined according to the present invention for increasing the yield and/or improving the vigor of an agricultural plant.
  • the present invention further provides a method for increasing the yield and/or improving the vigor of a plant, which comprises treating the plant, the locus where the plant is growing or is expected to grow, and/or the seeds from which the plant grows with a non-phytotoxic effective amount of component (A) and component (B) as defined herein.
  • the plant, the locus where the plant is growing or is expected to grow, and/or the seeds from which the plant grows are preferably treated simultaneously (together or separately) or subsequently with the components (A) and (B).
  • "increased yield" of an agricultural 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 present invention. According to the present invention, it is preferred that the yield be increased by at least 0,5 %, more preferred at least 1 %, even more preferred at least 2 %, still more preferred at least 4 %.
  • the terms "improved plant vigor” and “improved plant health” are synonyms, meaning that certain crop characteristics 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 present invention, such as: delay of senescence, root growth, longer panicles, increased or improved plant stand, the plant weight, plant height, emergence, improved visual appearance, protein content, oil content, starch content, more developed root system (improved root growth), reduced ethylene (reduced production and/or inhibition of reception), tillering increase, increase in plant height, bigger leaf blade, less dead basal leaves, stronger tillers, greener leaf color, pigment content, photosynthetic activity, less input needed (such as fertilizers or water), less seeds needed, enhanced plant vigor, more produc- tive tillers, earlier flowering, early grain maturity, less plant verse (lodging), increased shoot growth, increased plant stand and early and better germination, improved vitality of the plant, improved quality of the plant, improved quality of
  • Advantageous properties, obtained especially from treaded seeds are e.g. improved germination and field establishment, better vigor, more homogen field establishment.
  • Advantageous properties, obtained especially from foliar and/or in-furrow application are e.g. improved plant growth and plant development, better growth, more tillers, greener leaves, larger leaves, more biomass, better roots, improved stress tolerance of the plants, more grain yield, more biomass harvested, improved quality of the harvest (content of fatty acids, metabolites, oil etc.), more marketable products (e.g. improved size), improved process (e.g. longer shelf- life, better extraction of compounds), improved quality of seeds (for being seeded in the following seasons for seed production); or any other advantages familiar to a person skilled in the art.
  • the improvement of the plant vigor according to the present invention particularly means that the improvement of any one or several or all of the above mentioned plant characteristics are improved independently of or in combination with the pesticidal action of the composition or active ingredients.
  • the inventive compositions are used for yield increase of an agricultural plant.
  • the inventive compositions are used for improved tolerance against stress factors such as fungi, bacteria, viruses and/or insects and stress factors such as heat stress, cold stress, drought stress, UV stress and/or salt stress of an agricultural plant.
  • stress factors such as fungi, bacteria, viruses and/or insects
  • stress factors such as heat stress, cold stress, drought stress, UV stress and/or salt stress of an agricultural plant.
  • the treatment is made to vegetables and field crops.
  • the treatment is made to cereals such as for example wheat, barley or rye.
  • the method of the invention can be applied to field crops, such as soybeans, corn, cotton, wheat, barley, rye, rice, sugar beets, sugar cane and/or oilseed rape, in particular soybeans, corn, cotton, tobacco, common beans, wheat, barley, rye, peas, and others.
  • the method is preferably applied by treating the seeds or the plants. In this embodiment it may be preferred that the plants are treated with two to three applications per season.
  • the treatment is made to potatoes, tomatoes, cucurbits, cucumbers, melons, watermelons, garlic, onions, bananas, peanuts, carrots, cabbage, peppers, common beans, peas, lentils and/or lettuce, in particular potatoes, tomatoes, cucurbits, cucumbers, melons, watermelons, garlic, onions, and/or lettuce.
  • the treatment is made to apples, pears, stone fruits, or citrus, in particular apples, stone fruits, and/or citrus.
  • the treatment is made to strawberries, cherries, almonds, mango, papaya, blueberries and/or grapes in particular strawberries and/or cherries.
  • the treatment is made to turf and/or ornamentals. According to another embodiment of the described methods of the invention, the treatment is made to tea, tobacco and/or coffee.
  • the treatment is made to soybean, sugarcane, corn, cotton, wheat, barley, rye, rice, sugar beets or oilseed rape.
  • inventive mixtures can also be employed in treatment of plants or plant parts (such as seed) which are resistant to herbicides from the group consisting of the sulfonylureas, imidazolinones, glufosinate-ammonium or glyphosate-isopropylammonium and analogous active substances (see for example, EP-A-0242236, EP-A-242246) (WO 92/00377) (EP-A-0257993, U.S. Pat. No. 5,013,659) or in transgenic crop plants, for example cotton, with the capability of producing Bacillus thuringiensis toxins (Bt toxins) which make the plants resistant to certain pests (EP-A-0142924, E P-A-0193259).
  • herbicides from the group consisting of the sulfonylureas, imidazolinones, glufosinate-ammonium or glyphosate-isopropylammonium and analogous active substances
  • the mixtures can be used also for the treatment of plants or plant parts (such as seed) which have modified characteristics in comparison with existing plants consist, which can be generated for example by traditional breeding methods and/or the generation of mutants, or by recombinant procedures).
  • plants or plant parts such as seed
  • modified characteristics in comparison with existing plants consist, which can be generated for example by traditional breeding methods and/or the generation of mutants, or by recombinant procedures.
  • a number of cases have been described of recombinant modifications of crop plants for the purpose of modifying the starch synthesized in the plants (e.g. WO 92/1 1376, WO 92/14827, WO 91/19806) or of transgenic crop plants having a modified fatty acid composition (WO 91/13972).
  • two to ten, three to eight or four to six treatments with component (A) and at least one component (B) are made during a season.
  • the inventive composition is applied via the leaves or to the soil.
  • the treatment(s) are carried out as foliar application.
  • the method according to the invention is carried out as foliar application or spray application, respectively.
  • one, two, three, four, five and up to ten applications during one season are carried out, specifically more than two applications, and up to 10 applications. Also preferred more than two applications, and up to 5 applications during a season are carried out.
  • the inventive compositions are also suitable for dressing applications on plant propa- gation material.
  • the latter term embraces seeds of all kinds (fruit, tubers, grains), cuttings, cut shoots and the like.
  • One particular field of application is the treatment of all kinds of seeds.
  • the method according to the invention is preferably carried out as foliar application when applied to fruit and vegetables, such as potatoes, tomatoes, cucurbits, preferably cucumbers, melons, watermelons, garlic, onions, and lettuce.
  • Preferably more than two applications and up to 5 or up to 10 applications during a season are carried out.
  • the method according to the invention is preferably carried out as foliar application when applied to soybean, sugarcane, corn, cotton, wheat, barley, rye, rice, sugar beets or oilseed rape.
  • the application rates are usually from 10 g to 2000 g, preferably up to 1000 g of active ingredient per hectare.
  • the present invention relates to seed, comprising one of the inventive compositions as defined herein in an amount of from 0,1 g to 1000 g per 100 kg of seeds.
  • the present invention relates to the use of the in- ventive compositions for reducing the stress response of a plant while in parallel combating phytopathogenic fungi which comprises treating a site, for example a plant or a plant propagation material, that is infested or liable to be infested by fungi with the inventive compositions, in any desired sequence or simultaneously, that is, jointly or separately.
  • a site for example a plant or a plant propagation material
  • inventive compositions in any desired sequence or simultaneously, that is, jointly or separately.
  • Puccinia species on cereals and corn e.g. Puccinia recondita
  • Pyrenophora species on cereals e.g. Pyrenophora (syn. Drechslera) teres
  • Rhizoctonia species on cotton, rice, potatoes, lawns, corn, rapeseed, potatoes, sugar beet, vegetables and other plants
  • the present invention relates to the use of the inventive compositions for reducing the stress response of a plant while in parallel combating pests such as insects in agriculture. They are particularly suitable for controlling the following harmful insects from the order of
  • lepidopterans for example Agrotis ypsilon, Agrotis segetum, Alabama argillacea, Anticarsia gemmatalis, Argyresthia conjugella, Autographa gamma, Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheimatobia brumata, Choristoneura fumiferana, Choristoneura occidentalis, Cirphis unipuncta, Cydia pomonella, Den- drolimus pini, Diaphania nitidalis, Diatraea grandiosella, Earias insulana, Elasmopalpus lignosellus, Eupoecilia ambiguella, Evetria bouliana, Feltia subterranea, Galleria mel- Ionella, Grapholitha funebrana, Grapholitha molesta, Heliothis armigera, Heli
  • beetles Coldeoptera
  • Agrilus sinuatus for example Agrilus sinuatus, Agriotes lineatus, Agriotes obscu- rus, Amphimallus solstitialis, Anisandrus dispar, Anthonomus grandis, Anthonomus pomorum, Atomaria linearis, Blastophagus piniperda, Blitophaga undata, Bruchus rufi- manus, Bruchus pisorum, Bruchus lentis, Byctiscus betulae, Cassida nebulosa, Cero- toma trifurcata, Ceuthorrhynchus assimilis, Ceuthorrhynchus napi, Chaetocnema tibialis, Conoderus vespertinus, Crioceris asparagi, Diabrotica Iongicornis, Diabrotica spe- ciosa, Diabrotica 12-punctata, Diabrotica virgifera, Diloboderus ab
  • dipterans dipterans
  • Aedes aegypti Aedes vexans, Anastrepha ludens, Anopheles maculipennis, Ceratitis capitata, Chrysomya bezziana, Chrysomya homi- nivorax, Chrysomya macellaria, Contarinia sorghicola, Cordylobia anthropophaga, Culex pipiens, Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Fannia canicu- laris, Gasterophilus intestinalis, Glossina morsitans, Haematobia irritans, Haplodiplosis equestris, Hylemyia platura, Hypoderma lineata, Liriomyza sativae, Liriomyza trifolii, Lucilia caprina, Lucilia cuprina, Lucilia sericata, Lycor
  • hymenopterans e.g. Acromyrmex ambuguus, Acromyrmex cras- sispinus, Acromyrmex heiery, Acromyrmex landolti, Acromyrmex subterraneus, Athalia rosae, Atta capiguara, Atta cephalotes, Atta laevigata, Atta robusta, Atta sexdens, Atta texana, Hoplocampa minuta, Hoplocampa testudinea, Monomorium pharaonis, So- lenopsis geminata and Solenopsis invicta,
  • Hymenoptera e.g. Acromyrmex ambuguus, Acromyrmex cras- sispinus, Acromyrmex heiery, Acromyrmex landolti, Acromyrmex subterraneus, Athalia rosae, Att
  • Heteroptera e.g. Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dichelops furcatus, Dysdercus cingulatus, Dysdercus intermedius, Euchistos hems, Eurygaster integriceps, Euschistus impictiventris, Leptoglossus phyllopus, Lygus lineolaris, Lygus pratensis, Nezara viridula, Piesma quadrata, Piezodorus guildini, Solubea insularis and Thyanta perditor,
  • Heteroptera e.g. Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dichelops furcatus, Dysdercus cingulatus, Dysdercus intermedius, Euchistos hems, Eurygaster integriceps, Euschistus im
  • Hemiptera and Homoptera e.g. Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Diaphorina citri, Dysdercus cingulatus, Dysdercus intermedius, Eurygaster integriceps, Euschistus impictiventris, Leptoglossus phyllopus, Lygus lineolaris, Lygus pratensis, Nezara viridula, Piesma quadrata, Solubea insularis , Thyanta perditor, Acyrthosiphon onobrychis, Adelges laricis, Aphidula nasturtii, Aphis fabae, Aphis forbesi, Aphis pomi, Aphis gossypii, Aphis grossulariae, Aphis schneideri, Aphis spi- raecola, Aphis
  • Dysaulacorthum pseudosolani Dysaphis plantaginea, Dysaphis pyri, Empoasca fabae, Hyalopterus pruni, Hyperomyzus lactucae, Macrosiphum avenae, Macrosiphum eu- phorbiae, Macrosiphon rosae, Megoura viciae, Melanaphis pyrarius, Metopolophium dirhodum, Myzodes persicae, Myzus ascalonicus, Myzus cerasi, Myzus varians, Na- sonovia ribis-nigri, Nilaparvata lugens, Pemphigus bursarius, Perkinsiella saccharicida, Phorodon humuli, Psylla mali, Psylla piri, Rhopalomyzus ascalonicus, Rhopalosiphum maidis, Rhopalosiphum padi, Rhopalos
  • Isoptera e.g. Calotermes flavicollis, Cornitermes cumulans, Heterotermes tenuis, Leucotermes flavipes, Neocapritemes opacus, Procornitermes triacifer; Reticu- litermes lucifugus, Syntermes molestus, and Termes natalensis,
  • orthopterans e.g. Acheta domestica, Blatta orientalis, Blattella germanica, Forficula auricularia, Gryllotalpa gryllotalpa, Locusta migratoria, Melanoplus bivittatus, Melanoplus femur-rubrum, Melanoplus mexicanus, Melanoplus sanguinipes, Melano- plus spretus, Nomadacris septemfasciata, Periplaneta americana, Schistocerca ameri- cana, Schistocerca pereg ⁇ na, Stauronotus maroccanus and Tachycines asynamorus,
  • Arachnoidea such as arachnids, e.g. of the families Argasidae, Ixodidae and Sarcopti- dae, such as Amblyomma americanum, Amblyomma variegatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Dermacentor silva- rum, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Ornithodorus moubata, Otobius megnini, Dermanyssus gallinae, Psoroptes ovis, Rhipicephalus appendicula- tus, Rhipicephalus evertsi, Sarcoptes scabiei, and Eriophyidae spp.
  • arachnids e.g. of the families Argasidae, Ixodidae and Sarcopti- da
  • Tetranychidae spp. such as Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius and Tetranychus urticae, Panonychus ulmi, Panonychus citri, and oligonychus pratensis;
  • Thrips e.g. Frankliniella fusca, Frankliniella occidentalis, Frankliniella schultzei, Frankliniella tritici, Scirtothrips citri, Thrips oryzae, Thrips palmi and Thrips tabaci.
  • inventive mixtures are suitable for reducing stress responses in plants while combating pests of the orders Coleoptera, Lepidoptera, Thysanoptera, Homop- tera, Isoptera, and Orthoptera.
  • the active ingredient mixtures of the invention can be used in the form of premix formulations or the active ingredients can be applied to the area, plant or seed to be treated simultaneously or in immediate succession, if desired together with further carriers, surfactants or other application-promoting adjuvants customarily employed in formulation technology.
  • the inventive composition can contain an agriculturally acceptable carrier and/or vehicle.
  • the composition may be in solid form, for example in the form of a powder or granules, or in liquid form, for example in the form of an aqueous solution.
  • the active ingredients or compositions used according to the present invention can be converted into the formulations conventionally used for pesticides, for example solutions, emulsions, suspensions, dusts, powders, pastes and granules.
  • the use form depends on the particular purpose; in any case, it should ensure fine and uniform distribution of the compound according to the invention.
  • the present invention furthermore provides a composition as described above with at least one solid or liquid carrier.
  • compositions generally comprise from 0.1 to 95%, preferably from 0.5 to 90%, by weight of active ingredient.
  • the mixture comprising component (A) and component (B) is applied in a weight ratio of from 1 :2000 to 100:1.
  • the mixture comprising component (A) and component (B) is usually applied in a weight ratio of from 1 :1000 to 4:1.
  • the mixture comprising component (A) and component (B) is usually applied in a weight ratio of from 1 :100 to 2:1.
  • the non-phytotoxic amounts of the mixture applied are, depending on the kind of effect desired, the plant or plant part treated and the environmental conditions under which the plant or plant parts are growing, from 0.01 g to 200O g per ha.
  • the application rates of component (A) are from 0.01 g to 1000 g/ha.
  • the application rates of component (A) are from 5 to 500 g/ha.
  • the application rates of component (A) are from 10 to 100 g/ha.
  • the application rates of component (B) are, depending on the specific nature of the compound used, from 1 g to 3000 g/ha.
  • the application rates of component (B) are, depending on the specific nature of the compound used, from 10 to 1500 g/ha. According to another embodiment of the present invention, the application rates of component (B) are, depending on the specific nature of the compound used, from 20 to 750 g/ha.
  • Seed can be treated by methods known to the person skilled in the art, such as, for example, seed dressing, seed coating, seed dusting, seed soaking and seed pelleting.
  • the amounts of active ingredient employed are generally from 1 to 1000 g/100 kg of seed, preferably from 1 to 200 g/100 kg, in particular from 1 to 100 g/100 kg.
  • the amount of active ingredient applied depends on the kind of application area and on the desired effect. Amounts customarily applied in the protection of materials are, for example, 0.001 g to 2000 g, preferably 0.005 g to 1000 g, of active compound per cubic meter of treated material.
  • the formulations are prepared in a known manner, for example by extending the active compound with solvents and/or carriers, if desired using emulsifiers and dispersants.
  • Solvents/auxiliaries which are suitable are essentially:
  • aromatic solvents for example Solvesso products, xylene
  • paraffins for example mineral oil fractions
  • alcohols for example methanol, butanol, pentanol, benzyl alcohol
  • ketones for example cyclohexanone, gamma- butyrolactone
  • pyrrolidones NMP, NOP
  • acetates glycols, fatty acid dimethylamides, fatty acids and fatty acid esters.
  • solvent mixtures may also be used, carriers such as ground natural minerals (for example kaolins, clays, talc, chalk) and ground synthetic minerals (for example finely divided silica, silicates); emulsifiers such as nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates) and dispersants such as lignosulfite waste liquors and methylcellulose.
  • ground natural minerals for example kaolins, clays, talc, chalk
  • ground synthetic minerals for example finely divided silica, silicates
  • emulsifiers such as nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates) and dispersants such as lignosulfite waste liquors and methylcellulose.
  • Suitable surfactants are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl polygly
  • 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, for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, strongly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone and water.
  • 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, for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, m
  • Powders, materials for spreading and dustable products can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.
  • Granules for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds 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, for example, 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 silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth
  • Formulations for seed treatment may further comprise binders and/or gelants and if appropriate dyes.
  • Binders can be added to increase the adhesion of the active compounds to the seed after the treatment.
  • Suitable binders are for example EO/PO block copolymer surfactants, but also polyvinyl alcohols, polyvinylpyrrolidones, polyacrylates, polymethacry- lates, polybutenes, polyisobutylenes, polystyrenes, polyethyleneamines, polyethyl- eneamides, polyethyleneimines (Lupasol®, Polymin®), polyethers, polyurethanes, polyvinyl acetates, Tylose and copolymers of these polymers.
  • a suitable gelant is for example carrageen (Satiagel®).
  • the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active compound.
  • the active compounds are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
  • Component (A) (1-methylcyclopropene) may be present in form of a complex.
  • Com- plexing agents comprise inorganic or organic chelating agents, preferably organic chelating agents such as sugars (for example cyclodextrins).
  • 1-methylcyclopropene (component A) may also be used in a variety of other formulations.
  • concentrations of active compound in the ready-to-use preparations can be varied within relatively wide ranges. In one embodiment of the present invention, they are from 0.0001 to 10%. In another embodiment of the present invention, they arefrom 0.001 to 1 %.
  • the active compounds can also be used with great success in the ultra-low-volume (ULV) process, it being possible to apply formulations with more than 95% by weight of active compound or even the active compound without additives.
  • UUV ultra-low-volume
  • the formulations in question give, after two-to-tenfold dilution, active compound concentrations of from 0.01 to 60% by weight, preferably from 0.1 to 40% by weight, in the ready-to-use preparations.
  • a Water-soluble concentrates (SL, LS)
  • active ingredient 10 parts by weight of active ingredient are dissolved with 90 parts by weight of water or with a water-soluble solvent.
  • wetters or other auxiliaries are added.
  • the active compound dissolves upon dilution with water. This gives a formulation having an active compound content of 10% by weight.
  • DC Dispersible concentrates
  • Water-dispersible granules and water-soluble granules 50 parts by weight of active ingredient are ground finely with addition of 50 parts by weight of dispersants and wetters and made into water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluid- ized bed). Dilution with water gives a stable dispersion or solution of the active compound.
  • the formulation has an active compound content of 50% by weight.
  • Water-dispersible powders and water-soluble powders 75 parts by weight of active ingredient are ground in a rotor-stator mill with addition of 25 parts by weight of dispersants, wetters and silica gel. Dilution with water gives a stable dispersion or solution of the active compound.
  • the active compound content of the formulation is 75% by weight.
  • H Dustable powders (DP, DS) 5 parts by weight of active ingredient are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dustable product with an active compound content of 5% by weight.
  • I Granules 0.5 part by weight of active ingredient is ground finely and associated with 99.5 parts by weight of carriers. Current methods are extrusion, spray-drying or the fluidized bed. This gives granules with an active compound content of 0.5% by weight to be applied undiluted.
  • Seed treatment typically utilizes water-soluble concentrates (LS), suspensions (FS), dusts (DS), water-dispersible and water-soluble powders (WS, SS), emulsions (ES), emulsifiable concentrates (EC) and gel formulations (GF). These formulations can be applied neat or preferably diluted to the seed. The application can take place prior to sowing.
  • LS water-soluble concentrates
  • FS suspensions
  • DS dusts
  • WS, SS water-dispersible and water-soluble powders
  • ES emulsions
  • EC emulsifiable concentrates
  • GF gel formulations
  • Such formulations typically comprise from 1 to 800 g/l of active compound, from 1 to 200 g/l of surfactants, from 0 to 200 g/l of antifreeze, from 0 to 400 g/l of binder, from 0 to 200 g/l of dyes and solvent, preferably water.
  • the active compounds can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring.
  • the use forms depend entirely on the intended purposes; the intention is to ensure in each case the finest possible distribution of the active compounds used according to the invention.
  • Aqueous use 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 wetting agent, tackifier, dispersant or emulsifier.
  • tackifier tackifier
  • dispersant or emulsifier can be homogenized in water by means of a wetting agent, 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 compound 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 0.01 to 1 %.
  • the active compounds may also be used successfully in the ultra-low-volume process (ULV), by which it is possible to apply formulations comprising over 95% by weight of active compound, or even to apply the active compound without additives.
  • UUV ultra-low-volume process
  • oils, wetters, adjuvants may be added to the active compounds, if appropriate not until immediately prior to use (tank mix).
  • These agents can be admixed with the agents according to the invention in a weight ratio of 1 :100 to 100:1 , preferably 1 :10 to 10:1.
  • Suitable adjuvants in this sense are in particular: organically modified polysiloxanes, for example Break Thru S 240 ® ; alcohol alkoxylates, for example Atplus 245 ® , Atplus MBA 1303 ® , Plurafac LF 300 ® and Lutensol ON 30 ® ; EO/PO block polymers, for example Pluronic RPE 2035 ® and Genapol B ® ; alcohol ethoxylates, for example Lutensol XP 80 ® ; and sodium dioctylsulfosuccinate, for example Leophen RA ® .
  • the mixtures contain 1-methylcyclopropene together with a metal-chelating agent as described in US 2005/0261132 or an encapsulating agent as described in US 2005/0261131.
  • the active ingredients were used as formulations.
  • the formulations were diluted to the concentrations given in the respective examples.
  • the different treatments were evaluated by estimating the infected leaf area in percent. Mean percentage of infected leaf area was calculated for each treatment and translated in efficacy of pathogen control expressed as percent of the untreated control.
  • ⁇ corresponds to the fungicidal infection of the treated plants in % and ⁇ corresponds to the fungicidal infection of the untreated (control) plants in %
  • An efficacy of 0 means the infection level of the treated plants corresponds to that of the untreated control plants; an efficacy of 100 means the treated plants were not infected.
  • the expected efficacies of the combinations of the active compounds were estimated using Colby ' s formula (Colby, S. R., Calculating synergistic and antagonistic responses of herbicide combinations, Weeds, 1J5, pp. 20-22, 1967) and compared with the observed efficacies.
  • E expected efficacy expressed in % of the untreated control, when using the mix- ture of the active compounds A and B at the concentrations a and b x efficacy, expressed in % of the untreated control, when using the active ingredient A at the concentration a y efficacy, expressed in % of the untreated control, when using the active ingredient B at the concentration b
  • the spray solutions were prepared in several steps: First, a stock solution was prepared by mixing acetone and/or DMSO and the wetting agent/emulsifier Uniperol, which is based on ethoxylated alkylphenoles, in a ratio (volume) solvent to emulsifier of 99 to 1. Subsequently, the above-described solvent/emulsifier mixture was added to 25 mg of the active compound to give a total volume of 10 ml. Consequently, water was added to give a total volume of 100 ml. Finally, the prepared stock solution was diluted with the above described solvent-emulsifier-water mixture to the concentration needed.
  • Uniperol the wetting agent/emulsifier Uniperol
  • the first fully developed leaves of pot grown barley plants were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient mentioned in the table 1 below.
  • the treated plants were inoculated with an aqueous spore suspension of Pyrenophora (syn. Drechslera) teres.
  • the trial plants were immediately transferred to a humid chamber in the greenhouse. After 6 days of cultivation at 20-24 0 C and a relative humidity close to 70%, the extent of fungal attack on the leaves was visually assessed as % leaf area.
  • the spray solutions were prepared in several steps: First a stock solution was prepared by dissolving 200 mg of the active ingredients in an aqueous solution containing 1 % (v/v) of Atplus and 0.1 % (v/v) of Silwet L77. Subsequently, these stock solutions were further diluted to the concentrations needed using the aqueous solution described. Primary leaves and first trifoliate leaves of soybean plants grown in pots under greenhouse conditions were sprayed with the respective dilutions of the given concentrations of active ingredients (table 2). Spray volume corresponded to 350 I/ha. The spray film was allowed to dry for 24 h, and then the plants were inoculated with a spore suspension of soybean rust.
  • the plants were incubated in a growth chamber in the dark over night at high humidity (90 to 95%) and 22 to 24°C to allow the spores to germinate and to penetrate the leafs. The next day the plants were transferred to the greenhouse and kept there at 22 to 24 0 C and a relative humidity of 80 to 90 %. After 14 days the brown rust infection was scored as % infection of the total leaf area of primary leaves and first trifoliate leaves.
  • Results The non-treated control plants displayed an infestation rate of 81 %.
  • Soybean plants are raised under greenhouse conditions with two plants each per 12-cm pot. Spray treatments of the leaves are carried out with a volume of liquid of 750 I/ha when the plants have developed one to two trifoliate leaves. 24 hours after treatment, the shoots of the soybean plants are dissected above the cotyledons and wilted for 10 minutes under laboratory conditions. Shoots representing a distinct treatment are incubated for 60 minutes under laboratory conditions in a 100-ml Erlenmeyer flask sealed with a rubber cap. Thereafter, gas samples are taken and analyzed for their ethylene content by gas chromatography.

Abstract

La présente invention concerne des mélanges agrochimiques comprenant du 1-méthylcyclopropène en tant que composant (A) et en tant que composant (B) au moins un composé actif choisi parmi les ingrédients actifs tels que définis dans la description. L'invention concerne également un procédé d'amélioration du rendement, de la santé des plantes et/ou de la vigueur d'une plante agricole.
EP07857421A 2006-12-15 2007-12-11 Mélanges comprenant du 1-méthylcyclopropène Withdrawn EP2164323A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP10176165A EP2258177A3 (fr) 2006-12-15 2007-12-11 Mélanges contenant du methylcyclopropène
EP07857421A EP2164323A1 (fr) 2006-12-15 2007-12-11 Mélanges comprenant du 1-méthylcyclopropène

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP06126269 2006-12-15
EP07857421A EP2164323A1 (fr) 2006-12-15 2007-12-11 Mélanges comprenant du 1-méthylcyclopropène
PCT/EP2007/063734 WO2008071714A1 (fr) 2006-12-15 2007-12-11 Mélanges comprenant du 1-méthylcyclopropène

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EP10176165A Withdrawn EP2258177A3 (fr) 2006-12-15 2007-12-11 Mélanges contenant du methylcyclopropène

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