AU2013203660A1 - Pesticide composition comprising propamocarb-hydrochloride and an insecticide active substance - Google Patents

Abstract

The present invention relates to a pesticide composition intended for protecting plants, crops or seeds against phyto-pathogenic fungi or damaging insects, and the corresponding methods of 5 treatment using the said composition. More precisely, the subject of the present invention is a pesticide composition based on propamocarb-HCI, an insecticide active substance and optionally a further fungicide active substance. 42127131 (GHMatters) P80785.AU.1

Description

1 PESTICIDE COMPOSITION COMPRISING PROPAMOCARB-HYDROCHLORIDE AND AN INSECTICIDE ACTIVE SUBSTANCE This application is a divisional application of Australian Patent No. 2007338050, the contents of 5 which are incorporated herein by reference. DESCRIPTION The present invention relates to a pesticide composition intended for protecting plants, crops or seeds against fungal diseases or insect damages, and the corresponding methods of protection 10 by application of the said composition. More precisely, the subject of the present invention is a pesticide composition based on propamocarb-HCI and an insecticide active substance or compound and optionally a further fungicide active substance or compound. As regards pesticide activity, in particular for the protection of crops, one of the problems at the 15 heart of the research studies carried out in this technical field is the improvement of performances, in particular in terms of biological activity and in particular in terms of maintaining such an activity over time. The present invention provides a pesticide composition which can be used, in particular by the farmer, for controlling the pest infesting crops and in particular for controlling insects or diseases 20 of corn, beet, cotton, canola, beans, peanuts vegetables, lucerne, soybean, market garden crops, turf, wood, tree and horticultural plants, for example Pythium on corn. The pesticide compounds useful for the protection of plants must be endowed with an ecotoxicity which is reduced to the minimum. As far as possible, they should not be dangerous or toxic to the operator during use. The economic factor should of course not be overlooked in 25 the search for novel pesticide agents. Propamocarb-hydrochloride or propamocarb-HCI is a known compound having as chemical name propyl [3-(dimethylamino)propyl]carbamate hydrochloride and which is represented by the following formula: Cl O N N 30 0 Propamocarb moiety is described in British patent GB-1212708: activity is reported in controlling Pythium ultimum. This document is silent with regard to any result or biological activity of such potential mixtures. In particular, this document does not report any activity to specifically control seed diseases with propamocarb-HCI mixtures nor this document discloses any mixture of 35 propamocarb-HCI with any insecticide active substance. There is no mention in this document 42252761 (GHMatters) P80785.AU.1 2 of any particular result or biological activity of any mixture of propamocarb-HCI with an insecticide active substance. In international patent application WO-2006/024333 there are generically disclosed mixtures of 5 certain neonicotinoid insecticide compounds with known fungicide substances; propamocarb is part of long list of such known fungicide substances. However, there is no specific disclosure in this document of any combination comprising propamocarb. In international patent applications WO-2004/080181 and WO-2007/101547 there are 10 generically disclosed numerous mixtures of some phtalamide insecticide compounds with known fungicide substances. The association of these insecticide compounds with propamocarb has not been specifically disclosed nor has been subject to any experimentation. Such an association does not form part of the present invention. 15 In a main aspect, the present invention provides a composition comprising: A) propamocarb-HCI and B) an insecticide compound in an A/B weight ratio ranging from 1/1,000 to 1,000/1; provided that insecticide compound B differs from compounds of formula (I) Hal 0

CH

3 C SOCH H l O N S 2 CH3 H R

CF

3 H/ N F CF 0 20

H

3 C (I) wherein - Hal represents a chlorine atom, a bromine atom or a iodine atom; - R represents hydrogen or methyl and * may represent a carbon atom in R- or S 25 configuration. According to the present invention, propamocarb-HCI and propamocarb can be used in the same manner. Both forms are part of the present invention in its various aspects or preferences. The present invention advantageously provides a pesticide composition which is completely 30 high-performing in particular as regards its efficacy against pests and the perenniallity of this 4212713_1 (GHMatters) P80785.AU.1 3 efficacy so as to be able to reduce the doses of chemical products spread in the environment for combating pest damages or attacks of plants or crops. The invention provides a pesticide composition capable to be more active and active for longer, and which therefore has a lower dose, but which is also less toxic, in particular in the treatment 5 of plants and particularly the foliar and seed treatments of fungal diseases or the control of insects, for example, of cereals, cotton, peanut, bean, beet, canola, Solanaceae, grapevine, vegetables, lucerne, soybean, market garden crops, turf, wood or horticultural plants. The composition according to the invention allows controlling a broad variety of insects or fungi. For example, the pesticide composition according to the invention exhibits an improved efficacy 10 against fungus like Plasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Basidiomycetes, Deuteromycetes and Ascomycetes. All these objectives or advantages, among others, were achieved by finding a pesticide composition comprising propamocarb-HCI; an insecticide compound and optionally a further 15 fungicide compound. Such a composition surprisingly and unexpectedly allows a very high and perennial insecticide or anti-fungal efficacy against a broad spectrum of insects or fungi and in particular against those responsible for diseases or damages of corn for example to Oomycetes. Other insect pests or diseases of corn can be controlled with the pesticide composition according to the invention, in particular the control of Ascomycetes or 20 Basidiomycetes. The pesticide composition according to the invention may also be used for the treatment of bacterial or virus diseases. Insects or nematodes that can be controlled with the pesticide composition according to the invention include a broad variety of these damaging organisms. 25 For the composition according to the invention, insecticide compound B is preferably selected in the list consisting of: B1) a compound capable to act as an acetylcholine receptor agonist or antagonist, for example a compound of the type chloronicotinyl like acetamiprid, clothianidin, dinotefuran, 30 imidacloprid, imidaclothiz also known as (2E)-1-[(2-chloro-1,3-thiazol-5-yl)methyl]-N nitroimidazolidin-2-imine, nitenpyram, nithiazine, thiacloprid; thiamethoxam; nicotine, bensultap, cartap, (2E)-1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3,5-dimethyl-N-nitro-1,3,5-triazinan-2-imine; B2) a compound capable to inhibit acetylcholinesterase (ACHE), for example a compound of the type carbamate like alanycarb, aldicarb, aldoxycarb, allyxycarb, aminocarb, 35 bendiocarb, benfuracarb, bufencarb, butacarb, butocarboxim, butoxycarboxim, carbaryl, 4212713_1 (GHMatters) P80785.AU.1 4 carbofuran, carbosulfan, cloethocarb, dimetilan, ethiofencarb, fenobucarb, fenothiocarb, formetanate, furathiocarb, isoprocarb, metam-sodium, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, promecarb, propoxur, thiodicarb, thiofanox, trimethacarb, XMC, xylylcarb; triazamate ; a compound of the type organophosphate like acephate, azamethiphos, azinphos ( 5 methyl, -ethyl), bromophos-ethyl, bromfenvinfos (-methyl), butathiofos, cadusafos, carbopheno thion, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos (-methyl/-ethyl), coumaphos, cyanofenphos, cyanophos, chlorfenvinphos, demeton-s-methyl, demeton-s-methylsulphon, dialifos, diazinon, dichlofenthion, dichlorvos/ddvp, dicrotophos, dimethoate, dimethylvinphos, dioxabenzofos, disulfoton, epn, ethion, ethoprophos, etrimfos, famphur, fenamiphos, 10 fenitrothion, fensulfothion, fenthion, flupyrazofos, fonofos, formothion, fosmethilan, fosthiazate, heptenophos, iodofenphos, iprobenfos, isazofos, isofenphos, isopropyl o-salicylate, isoxathion, malathion, mecarbam, methacrifos, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion (-methyl/-ethyl), phenthoate, phorate, phosalone, phosmet, phosphamidon, phosphocarb, phoxim, pirimiphos (-methyl/-ethyl), 15 profenofos, propaphos, propetamphos, prothiofos, prothoate, pyraclofos, pyridaphenthion, pyridathion, quinalphos, sebufos, sulfotep, sulprofos, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, triclorfon, vamidothion; B3) a compound capable to modulate the sodium channel or to block the voltage dependant sodium channel, for example a compound of the type pyrethroid like acrinathrin, 20 allethrin (d-cis-trans, d-trans), beta-cyfluthrin, bifenthrin, bioallethrin, bioallethrin-s-cyclopentyl isomer, bioethanomethrin, biopermethrin, bioresmethrin, chlovaporthrin, cis-cypermethrin, cis resmethrin, cis-permethrin, clocythrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin (alpha, beta-, theta-, zeta-), cyphenothrin, deltamethrin, empenthrin (1R-isomer), esfenvalerate, etofenprox, fenfluthrin, fenpropathrin, fenpyrithrin, fenvalerate, flubrocythrinate, flucythrinate, 25 flufenprox, flumethrin, fluvalinate, fubfenprox, gamma-cyhalothrin, imiprothrin, kadethrin, lambda-cyhalothrin, metofluthrin, permethrin (cis-, trans-), phenothrin (1r-trans isomer), prallethrin, profluthrin, protrifenbute, pyresmethrin, resmethrin, RU15525, silafluofen, tau fluvalinate, tefluthrin, terallethrin, tetramethrin (-1r- isomer), tralomethrin, transfluthrin, ZX18901, pyrethrins (pyrethrum); for example DDT; for example a compound of the type oxadiazine like 30 indoxacarb; B4) a compound capable to modulate acetylcholine receptor, for example a compound of the type spinosyn like spinosad; B5) a compound capable to act as GABA-gated chloride channel antagonist, for example a compound of the type cyclodiene organochlorine like camphechlor, chlordane, 42127131 (GHMatters) P80785.AU.1 5 endosulfan, gamma-HCH, HCH, heptachlor, lindane, methoxychlor; a compound of the type fiprole like acetoprole, ethiprole, fipronil, vaniliprole; B6) a compound capable to activate the chloride channel, for example a compound of the type mectin like avermectin, emamectin, emamectin-benzoate, ivermectin, milbemycin; 5 B7) a compound capable to mimic a juvenile hormone like diofenolan, epofenonane, fenoxycarb, hydroprene, kinoprene, methoprene, pyriproxifen, triprene; B8) a compound capable to act as an ecdysone agonist or disruptor, for example a compound of the type diacylhydrazine like chromafenozide, halofenozide, methoxyfenozide, tebufenozide; 10 B9) a compound capable to inhibit chitin biosynthesis, for example a compound of the type benzoylurea like bistrifluron, chlofluazuron, diflubenzuron, fluazuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, penfluron, teflubenzuron, triflumuron; buprofezin; cyromazine; B10) a compound capable to inhibit oxidative phosphorylation or to disrupt ATP, like 15 diafenthiuron; for example a compound of the type organotin like azocyclotin, cyhexatin, fenbutatin-oxide; B11) a compound capable to uncouple oxidative phosphorylation via disruption of H proton gradient, for example a compound of the type pyrrole like chlorfenapyr; a compound of the type dinitrophenole like binapacyrl, dinobuton, dinocap, DNOC; 20 B12) a compound capable to inhibit site I electron transport, for example a compound of the type METI like fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad, tolfenpyrad; hydramethylnon; dicofol; B13) a compound capable to inhibit site 11 electron transport like rotenone; B14) a compound capable to inhibit site III electron transport like acequinocyl, 25 fluacrypyrim; B15) a compound capable to act as a microbial disruptor of insect midgut or intestinal membrane like stains of Bacillus thuringiensis; B16) a compound capable to inhibit lipid synthesis, for example a compound of the type tetronic acid insecticide like spirodiclofen, spiromesifen or a compound of the type tetramic acid 30 insecticide like spirotetramat also kown as carbonic acid cis-3-(2,5-dimethylphenyl)-8-methoxy 2-oxo-1 -azaspiro[4.5]dec-3-en-4-yl ethyl ester (CAS-reg-n*203313-25-1) and 3-(2,5 dimethylphenyl)-8-methoxy-2-oxo-1-azaspiro[4.5]dec-3-en-4-yl ethyl carbonate also known as carbonic acid 3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-1 -azaspiro[4.5]dec-3-en-4-yl ethyl ester (CAS-reg-n*382608-10-8) ; 35 B17) a compound of the type carboxamide like flonicamid; 4212713_1 (GHMatters) P80785.AU.1 6 B18) a compound capable to act as an octopaminergic agonist like amitraz; B19) a compound capable to inhibit magnesium-stimulated ATP-ase like propargite; B20) a compound of the type BDCA or capable to act as a ryanodin receptor agonist like rynaxypyr or phthalamides, e.g. flubendiamide also known as N2-[1,1-dimethyl-2 5 (methylsulfonyl)ethyl]-3-iodo-N1-[2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl] 1,2-benzenedicarboxamide (CAS-reg-n*272451-65-7); B21) a compound of the type nereistoxin analogue insecticide like thiocyclam hydrogen oxalate, thiosultap-sodium; 822) a compound of the types biologica, hormones or pheromones like azadirachtin, 10 Bacillus spec., Beauveria spec., codlemone, Metarrhizium spec., Paecilomyces spec., thuringiensin, Verticilium spec.; B23) a compound of unknown or non-specific mode of action, for example a compound of the type fumigant like aluminium phosphide, methyl bromide, sulfuryl fluoride; a compound of the type selective feeding blocker like cryolite, flonicamid, pymetrozine; a compound of the type 15 mite growth inhibitor like clofentezine, etoxazole, hexythiazox; amidoflumet, benclothiaz, benz oximate, bifenazate, bromopropylate, buprofezin, chinomethionat, chlordimeform, chloro benzilate, chloropicrin, clothiazoben, cycloprene, cyflumetofen, dicyclanil, fenoxacrim, fentrifanil, flubendiamide, flubenzimine, flufenerim, flutenzin, gossyplure, hydramethylnone, japonilure, metoxadiazone, petroleum, piperonyl butoxide, potassium oleate, pyrafluprole, pyridalyl, 20 pyriprole, sulfluramid, tetradifon, tetrasul, triarathene, verbutin. More preferrably, the composition according to the invention comprises propamocarb-HCI and abamectin ; propamocarb-HCI and acephate; propamocarb-HCI and acetamiprid; propamocarb HCI and acrinathrin; propamocarb-HCI and aldicarb; propamocarb-HCI and alpha-cypermethrin; 25 propamocarb-HCI and beta-cyfluthrin; propamocarb-HCI and bifenthrin; propamocarb-HCI and carbaryl; propamocarb-HCI and carbofuran; propamocarb-HCI and chlorfenapyr; propamocarb HCI and chlorfluazuron; propamocarb-HCI and chlorpyrifos-E; propamocarb-HCI and clothianidin; propamocarb-HCI and cyfluthrin; propamocarb-HCI and cypermethrin; propamocarb-HCI and cyromazine; propamocarb-HCI and deltamethrin; propamocarb-HCI and 30 diflubenzuron; propamocarb-HCI and dinotefuran; propamocarb-HCI and emamectin-benzoate; propamocarb-HCI and ethiprole; propamocarb-HCI and fenpyroximate; propamocarb-HCI and fipronil; propamocarb-HCI and flonicamid; propamocarb-HCI and flubendiamide; propamocarb HCI and flufenoxuron; propamocarb-HCI and gamma-cyhalothrin; propamocarb-HCI and hexaflumuron; propamocarb-HCI and imidacloprid; propamocarb-HCI and indoxacarb; 35 propamocarb-HCI and L-cyhalothrin; propamocarb-HCI and lepimectin; propamocarb-HCI and 42127131 (GHMatters) P80785.AU.1 7 lufenuron; propamocarb-HCI and methamidophos; propamocarb-HCI and methiocarb; propamocarb-HCI and methomyl; propamocarb-HCI and methoxyfenozide; propamocarb-HCI and milbemycin; propamocarb-HCI and nitenpyram; propamocarb-HCI and novaluron; propamocarb-HCI and profenofos; propamocarb-HCI and pymetrozine; propamocarb-HCI and 5 rynaxapyr; propamocarb-HCI and spinosad; propamocarb-HCI and spirodiclofen; propamocarb HCI and spiromesifen; propamocarb-HCI and spirotetramate; propamocarb-HCI and tebufenozide; propamocarb-HCI and tebufenozide; propamocarb-HCI and tebufenpyrad; propamocarb-HCI and tebufenpyrad; propamocarb-HCI and tebupirimphos; propamocarb-HCI and teflubenzuron; propamocarb-HCI and tefluthrin; propamocarb-HCI and thiacloprid; 10 propamocarb-HCI and thiamethoxam; propamocarb-HCl and thiodicarb; propamocarb-HCI and triazophos triflumuron; propamocarb-HCI and imidaclothiz; propamocarb-HCI and (2E)-1-[(2 chloro-1,3-thiazol-5-yl)methyl]-3,5-dimethyl-N-nitro-1,3,5-triazinan-2-imine. Even more preferrably, the composition according to the invention comprises propamocarb-HCI 15 and abamectin; propamocarb-HCI and acetamiprid; propamocarb-HCI and aldicarb; propamocarb-HCI and beta-cyfluthrin; propamocarb-HCI and carbofuran; propamocarb-HCI and chlorpyrifos-E; propamocarb-HCI and clothianidin; propamocarb-HCI and cypermethrin; propamocarb-HCI and cyromazine; propamocarb-HCI and deltamethrin; propamocarb-HCI and diflubenzuron; propamocarb-HCI and emamectin-benzoate; propamocarb-HCI and ethiprole; 20 propamocarb-HCI and fipronil; propamocarb-HCI and gamma-cyhalothrin; propamocarb-HCI and imidacloprid; propamocarb-HCI and L-cyhalothrin; propamocarb-HCI and lufenuron; propamocarb-HCI and methiocarb; propamocarb-HCI and methoxyfenozide; propamocarb-HCI and pymetrozine; propamocarb-HCI and rynaxapyr; propamocarb-HCI and spinosad; propamocarb-HCI and spirodiclofen; propamocarb-HCI and spiromesifen; propamocarb-HCI and 25 spirotetramate; propamocarb-HCI and tebufenozide; propamocarb-HCI and tebufenpyrad; propamocarb-HCI and tefluthrin; propamocarb-HCI and thiacloprid; propamocarb-HCI and thiamethoxam; propamocarb-HCI and thiodicarb; propamocarb-HCI and triflumuron; propamocarb-HCI and imidaclothiz; preferred composition according to the invention comprises propamocarb-HCI and (2E)-1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3,5-dimethyl-N-nitro-1,3,5 30 triazinan-2-imine. Still even more preferrably, the composition according to the invention comprises propamocarb HCI and abamectin; propamocarb-HCI and aldicarb; propamocarb-HCI and beta-cyfluthrin; propamocarb-HCI and chlorpyrifos-E; propamocarb-HCI and clothianidin; propamocarb-HCI and 35 cyromazine; propamocarb-HCI and deltamethrin; propamocarb-HCI and diflubenzuron; 4212713_1 (GHMatters) P80785.AU.1 8 propamocarb-HCI and emamectin-benzoate; propamocarb-HCI and fipronil; propamocarb-HCI and gamma-cyhalothrin; propamocarb-HCI and imidacloprid; propamocarb-HCI and L cyhalothrin; propamocarb-HCI and methiocarb; propamocarb-HCI and pymetrozine; propamocarb-HCI and rynaxapyr; propamocarb-HCI and spinosad; propamocarb-HCI and 5 spirodiclofen; propamocarb-HCI and spiromesifen; propamocarb-HCI and spirotetramate; propamocarb-HCI and tebufenozide; propamocarb-HCI and tebufenpyrad; propamocarb-HCI and tefluthrin; propamocarb-HCI and thiamethoxam; propamocarb-HCI and thiodicarb; propamocarb-HCI and imidaclothiz; propamocarb-HCI and (2E)-1-[(2-chloro-1,3-thiazol-5 yl)methyl]-3,5-dimethyl-N-nitro-1,3,5-triazinan-2-imine. 10 For the composition according to the invention the A/B weight ratio preferably ranges from 1/125 to 125/1; more preferably from 1/25 to 25/1. According to another aspect of the present invention, in the pesticide composition according to 15 the invention, the compound ratio A/B can be advantageously selected so as to produce a synergistic effect. The term synergistic effect is understood to mean in particular that defined by Colby in an article entitled "Calculation of the synergistic and antagonistic responses of herbicide combinations" Weeds, (1967), 15, pages 20-22. The latter article mentions the formula: 20 E=X+YXY 100 wherein E represents the expected percentage of inhibition of the pest for the combination of the two compounds at defined doses (for example equal to x and y respectively), X is the percentage of inhibition observed for the pest by compound A at a defined dose (equal to x), Y is the percentage of inhibition observed for the pest by compound B at a defined dose (equal to 25 y). When the percentage of inhibition observed for the combination is greater than E, there is a synergistic effect. The term "synergistic effect" also means the effect defined by application of the Tammes method, "Isoboles, a graphic representation of synergism in pesticides", Netherlands Journal of Plant Pathology, 70(1964), pages 73-80. 30 In a further aspect, the present invention provides a composition comprising: A) propamocarb-HCI; B) an insecticide compound and C) a further fungicide compound in an A/B/C weight ratio ranging from 1/1,000/1,000 to 35 1/0.001/0.001; provided that insecticide compound B differs from compounds of formula (1) 42127131 (GHMatters) P80785.AU.1 9 Hal O0 CH 3 SO2CH H R

CF

3 H/ N 5F CF 0

H

3 C (1) wherein - Hal represents a chlorine atom, a bromine atom or a iodine atom; 5 - R represents hydrogen or methyl and * may represent a carbon atom in R- or S configuration. In addition to propamocarb-HCI and an insecticide compound B as herein-defined, the composition according to the invention can comprise a further fungicide compound C preferably 10 selected in the list consisting of: Cl) a compound capable to inhibit the nucleic acid synthesis like benalaxyl, benalaxyl-M, bupirimate, clozylacon, dimethirimol, ethirimol, furalaxyl, hymexazol, mefenoxam, metalaxyl, metalaxyl-M, ofurace, oxadixyl, oxolinic acid ; C2) a compound capable to inhibit the mitosis and cell division like benomyl, carbendazim, 15 diethofencarb, ethaboxam, fuberidazole, pencycuron, thiabendazole, thiophanate-methyl, zoxamide; C3) a compound capable to inhibit the respiration for example as Cl-respiration inhibitor like diflumetorim ; as Cil-respiration inhibitor like boscalid, carboxin, fenfuram, flutolanil, furametpyr, 20 furmecyclox, mepronil, oxycarboxin, penthiopyrad, thifluzamide ; as CIll-respiration inhibitor like amisulbrom, azoxystrobin, cyazofamid, dimoxystrobin, enestrobin, famoxadone, fenamidone, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, trifloxystrobin ; C4) a compound capable of to act as an uncoupler like dinocap, fluazinam, meptyldinocap; 25 C5) a compound capable to inhibit ATP production like fentin acetate, fentin chloride, fentin hydroxide, silthiofam; 42127131 (GHMatters) P80785.AU.1 10 C6) a compound capable to inhibit AA and protein biosynthesis like andoprim, blasticidin-S, cyprodinil, kasugamycin, kasugamycin hydrochloride hydrate, mepanipyrim, pyrimethanil ; C7) a compound capable to inhibit the signal transduction like fenpiclonil, fludioxonil, quinoxyfen ; 5 C8) a compound capable to inhibit lipid and membrane synthesis like biphenyl, chlozolinate, edifenphos, etridiazole, iodocarb, iprobenfos, iprodione, isoprothiolane, procymidone, pyrazophos, tolclofos-methyl, vinclozolin ; C9) a compound capable to inhibit ergosterol biosynthesis like aldimorph, azaconazole, bitertanol, bromuconazole, cyproconazole, diclobutrazole, difenoconazole, diniconazole, 10 diniconazole-M, dodemorph, dodemorph acetate, epoxiconazole, etaconazole, fenarimol, fenbuconazole, fenhexamid, fenpropidin, fenpropimorph, fluquinconazole, flurprimidol, flusilazole, flutriafol, furconazole, furconazole-cis, hexaconazole, imazalil, imazalil sulfate, imibenconazole, ipconazole, metconazole, myclobutanil, naftifine, nuarimol, oxpoconazole, paclobutrazol, pefurazoate, penconazole, prochloraz, propiconazole, prothioconazole, pyributicarb, pyrifenox, 15 simeconazole, spiroxamine, tebuconazole, terbinafine, tetraconazole, triadimefon, triadimenol, tridemorph, triflumizole, triforine, triticonazole, uniconazole, viniconazole, voriconazole; C10) a compound capable to inhibit cell wall synthesis like benthiavalicarb, bialaphos, dimethomorph, flumorph, iprovalicarb, mandipropamid, polyoxins, polyoxorim, validamycin A; C11) a compound capable to inhibit melanine biosynthesis like carpropamid, diclocymet, 20 fenoxanil, phthalide, pyroquilon, tricyclazole; C12) a compound capable to induce a host defence like acibenzolar-S-methyl, probenazole, tiadinil ; C13) a compound capable to have a multisite action like Bordeaux mixture, captafol, captan, chlorothalonil, copper naphthenate, copper oxide, copper oxychloride, copper preparations 25 such as copper hydroxide, copper sulphate, dichlofluanid, dithianon, dodine, dodine free base, ferbam, fluorofolpet, folpet, guazatine, guazatine acetate, iminoctadine, iminoctadine albesilate, iminoctadine triacetate, mancopper, mancozeb, maneb, metiram, metiram zinc, oxine-copper, propineb, sulphur and sulphur preparations including calcium polysulphide, thiram, tolylfluanid, zineb, ziram; 30 C14) benthiazole, bethoxazin, capsimycin, carvone, chinomethionat, cufraneb, cyflufenamid, cymoxanil, dazomet, debacarb, dichlorophen, diclomezine, dicloran, difenzoquat, difenzoquat methylsulphate, diphenylamine, ethaboxam, ferimzone, flumetover, flusulfamide, fluopicolide, fluopyram also known as N-{2-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]ethyl}-2 (trifluoromethyl)benzamide, fluoroimide, fosetyl-aluminium, fosetyl-calcium, fosetyl-sodium, 35 hexachlorobenzene, 8-hydroxyquinoline sulfate, irumamycin, isotianil, methasulphocarb, 4212713_1 (GHMatters) P80785.AU.1 11 metrafenone, methyl isothiocyanate, mildiomycin, natamycin, nickel dimethyldithiocarbamate, nitrothal-isopropyl, octhilinone, oxamocarb, oxyfenthiin, pentachlorophenol and salts, 2 phenylphenol and salts, phosphorous acid and its salts, piperalin, propamocarb-fosetylate also known as dimethyl-[3-(propoxycarbonylamino)propyl]ammonium-O-ethylphosphonate, 5 propanosine-sodium, proquinazid, pyribencarb, pyrrolnitrine, quintozene, tecloftalam, tecnazene, triazoxide, trichlamide, valiphenal, zarilamid and 2,3,5,6-tetrachloro-4 (methylsulfonyl)-pyridine, N-(4-chloro-2-nitrophenyl)-N-ethyl-4-methyl-benzenesulfonamide, 2 amino-4-methyl-N-phenyl-5-thiazolecarboxamide, 2-chloro-N-(2,3-dihydro-1,1,3-trimethyl-1 H inden-4-yl)-3-pyridincarboxamide, 3-[5-(4-chlorophenyl)-2,3-dimethylisoxazolidin-3-yl]pyridine, 10 cis-1-(4-chlorophenyl)-2-(lH-1,2,4-triazole-1-yl)-cycloheptanol, methyl 1-(2,3-dihydro-2,2 dimethyl-1 H-inden-1-yl)-1 H-imidazole-5-carboxylate, 3,4,5-trichloro-2,6-pyridinedicarbonitrile, methyl-2-[[[cyclopropyl[(4-methoxyphenyl)imino]methyl]thio]methyl]-.alpha.

(methoxymethylene)-benzeneacetate, 4-chloro-alpha-propynyloxy-N-[2-[3-methoxy-4-(2 propynyloxy)phenyl]ethyl]-benzeneacetamide, (2S)-N-[2-[4-[[3-(4-chlorophenyl)-2-propynyl]oxy] 15 3-methoxyphenyl]ethyl]- 3-methyl-2-[(methylsulfonyl)amino]-butanamide, 5-chloro-7-(4 methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,4,6 trifluorophenyl)-N-[(1R)-1,2,2-trimethylpropyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amine, 5-chloro-N [(1R)-1,2-dimethylpropyl]-6-(2,4,6-trifluorophenyl)[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, N-[1-(5 bromo-3-chloropyridin-2-yl)ethyl]-2,4-dichloronicotinamide, N-(5-bromo-3-chloropyridin-2 20 yl)methyl-2,4-dichloronicotinamide, 2-butoxy-6-iodo-3-propyl-benzopyranon-4-one, N-{(Z) [(cyclopropylmethoxy)imino][6-(difluoromethoxy)-2,3-difluorophenyl]methyl}-2-phenylacetamide, N-{2-[1,1I'-bi(cyclopropyl)-2-yl]phenyl}-3-(difluoromethyl)-1 -methyl-1H-pyrazole-4-carboxamide,, N-ethyl-N-methyl-N'-{2-methyl-5-(trifluoromethyl)-4-[3 (trimethylsilyl)propoxy]phenyl}imidoformamide, N-ethyl-N-methyl-N'-{2-methyl-5 25 (difluoromethyl)-4-[3-(trimethylsilyl)propoxy]phenyl}imidoformamide, N-(3-ethyl-3,5,5-trimethyl cyclohexyl)-3-formylamino-2-hydroxy-benzamide, N-(4-chlorobenzyl)-3-[3-methoxy-4-(prop-2 yn-1-yloxy)phenyl]propanamide, N-[(4-chlorophenyl)(cyano)methyl]-3-[3-methoxy-4-(prop-2-yn 1 -yloxy)phenyl]propanamide, 2-[[[[1-[3(1 Fluoro-2 phenylethyl)oxy]phenyl]ethylidene]amino]oxy]methyl]-alpha-(methoxyimino)-N-methyl-alphaE 30 benzeneacetamide, N-(3',4'-dichloro-5-fluorobiphenyl-2-yl)-3-(difluoromethyl)-1-methyl-1H pyrazole-4-carboxamide, 2-(2-{[6-(3-chloro-2-methylphenoxy)-5-fluoropyrimidin 4-yl]oxy}phenyl)-2-(methoxyimino)-N-methylacetamide, 1-[(4-methoxyphenoxy)methyl]-2,2 dimethylpropyl-1H-imidazole-1- carboxylic acid, 0-[1-[(4-methoxyphenoxy)methyl]-2,2 dimethylpropyl]-1H-imidazole- 1- carbothioic acid, a dipeptic mixture of methyl-[S-(R,S)]-[3-(N 35 isopropoxycarbonylvalinyl)-amino]-3-(4-chloro-phenyl)propanoate, methyl-(2-chloro-5-{(1IE)-N 4212713_1 (GHMatters) P80785.AU.1 12 [(6-methylpyridin-2-yl)methoxy]-ethanimidoyl}benzyl)carbamate, 4-chloro-alpha-methoxy-N-[2 [3-methoxy-4-(2-propynyloxy)phenyl]ethyl]-benzeneacetamide, 3,4-dichloro-N-(2 cyanophenyl)isothiazole-5-carboxamide, N-[2-(1,3-dimethyl-butyl)-phenyl]-5-fluoro-1,3-dimethyl 1H-pyrazole-4-carboxamide. 5 Most preferred compounds C in the composition according to the invention can be selected in the list consisting of benalaxyl, benalaxyl-M, benthiavalicarb, carboxin, chlorothalonil, cyazofamid, cymoxanil, dimetomorph, fluazinam, fludioxonil, fluoxastrobin, fluquinconazole, flutriafol, fosetyl-AI, hexaconazole, hymexazol, ipconazole, mancozeb, mandipropamid, maneb, 10 mefenoxam, metalaxyl, metiram, penconazole, penthiopyrad, phosphorous acid, propamocarb fosetylate, propineb, prothioconazole, tebuconazole, thiram, triadimenol, trifloxystrobin, triticonazole and N-[2-(1,3-dimethyl-butyl)-phenyl]-5-fluoro-1,3-dimethyl-1 H-pyrazole-4 carboxamide. 15 The composition according to the invention preferably comprises A) propamocarb-HCI; B) an insecticide compound selected in the list consisting of abamectin, aldicarb, beta-cyfluthrin, chlorpyrifos-E, clothianidin, cyromazine, deltamethrin, diflubenzuron, emamectin-benzoate, fipronil, gamma-cyhalothrin, imidacloprid, L-cyhalothrin, methiocarb, 20 pymetrozine, rynaxapyr, spinosad, spirodiclofen, spiromesifen, spirotetramate, tebufenozide, tebufenpyrad, tefluthrin, thiamethoxam, thiodicarb, imidaclothiz, (2E)-1-[(2-chloro-1,3-thiazol-5 yl)methyl]-3,5-dimethyl-N-nitro-1,3,5-triazinan-2-imine and C) a further fungicide compound selected in the list consisting of benalaxyl, benalaxyl M, benthiavalicarb, carboxin, chlorothalonil, cyazofamid, cymoxanil, dimetomorph, fluazinam, 25 fludioxonil, fluoxastrobin, fluquinconazole, flutriafol, fosetyl-AI, hexaconazole, hymexazol, ipconazole, mancozeb, mandipropamid, maneb, mefenoxam, metalaxyl, metiram, penconazole, penthiopyrad, phosphorous acid, propamocarb-fosetylate, propineb, prothioconazole, tebuconazole, thiram, triadimenol, trifloxystrobin, triticonazole and N-[2-(1,3-dimethyl-butyl) phenyl]-5-fluoro-1,3-dimethyl-1 H-pyrazole-4-carboxamide. 30 For the composition according to the invention the A/B/C weight ratio preferably ranges from 1/100/100 to 1/0.01/0.01 more preferably from 1/80/80 to 1/0.05/0.05 ; even more preferably from 1/50/100 to 1/1.5/2.5 still even more preferably from 1/12/25 to 1/6/12. 42127131 (GHMatters) P80785,AU.1 13 According to another aspect of the present invention, in the pesticide composition according to the invention, the compound ratio A/B/C can be advantageously selected so as to produce a synergistic effect. The term synergistic effect is understood to mean in particular that defined by Colby in an article entitled "Calculation of the synergistic and antagonistic responses of 5 herbicide combinations" Weeds, (1967), 15, pages 20-22. The latter article mentions the formula: E = X+Y +Z -XYZ 100 wherein E represents the expected percentage of inhibition of the pest for the combination of the three compounds at defined doses (for example equal to x, y and z respectively), X is the 10 percentage of inhibition observed for the pest by compound A at a defined dose (equal to x), Y is the percentage of inhibition observed for the pest by compound B at a defined dose (equal to y) and Z is the percentage of inhibition observed for the pest by compound C at a defined dose (equal to z). When the percentage of inhibition observed for the combination is greater than E, there is a synergistic effect. 15 The term "synergistic effect" also means the effect defined by application of the Tammes method, "Isoboles, a graphic representation of synergism in pesticides", Netherlands Journal of Plant Pathology, 70(1964), pages 73-80. The pesticide composition according to the invention may comprise from 0.00001 to 100%, 20 preferably from 0.001 to 80%, of active compounds, whether these compounds are combined, or whether they are in the form of two or more active ingredients used separately. More generally, the pesticide composition according to the invention may eventually also comprise one or more other active substances selected from fungicide, herbicide, insecticide or plant growth regulator active compounds. 25 In addition to these additional active agents, the pesticide composition according to the invention may also comprise any other adjuvants or auxiliary agent useful in plant protection formulations such as, for example, an agriculturally suitable inert carrier and optionally an agriculturally suitable surfactant. For its practical use, the pesticide composition according to the invention can be used alone or 30 in formulations containing one or the other of the active ingredients or alternatively both of them together, in combination or association with one or more other compatible components which are, for example, solid or liquid fillers or diluents, adjuvants, surfactants or equivalents, which are suitable for the desired use and which are acceptable for uses in agriculture. The formulations can be of any type known in the sector that is suitable for application onto all types 4212713_1 (GHMatters) P80785.AU.1 14 of cultures or crops. These formulations, which can be prepared in any manner known by the skilled person, also form part of the invention. The formulations may also contain ingredients of other types, such as protective colloids, adhesives, thickeners, thixotropic agents, penetrating agents, oils for spraying, stabilisers, 5 preserving agents (in particular mould-proofing or biocide agents), sequestering or chelating agents or the like. More generally, the compounds used in the invention can be combined with any solid or liquid additives corresponding to the usual formulation techniques. The term "filler" means an organic or inorganic, natural or synthetic component with which the active components are combined to facilitate its application, for example, onto the plants, the 10 seeds or the soil. This filler is consequently generally inert and it must be acceptable (for example acceptable for agronomic uses, in particular for treating plants). The filler can be solid, for example clays, natural or synthetic silicates, silica, resins, waxes, solid fertilizers (for example ammonium salts), natural soil minerals, such as kaolins, clays, talc, lime, quartz, attapulgite, montmorillonite, bentonite or diatomaceous earths, or synthetic 15 minerals, such as silica, alumina or silicates, in particular aluminium or magnesium silicates. The solid fillers which are suitable for granules are as follows: natural, crushed or broken rocks, such as calcite, marble, pumice, sepiolite and dolomite; synthetic granules of inorganic or organic flours; granules of organic material such as sawdust, coconut shell, corn ear or envelope, or tobacco stem; kieselguhr, tricalcium phosphate, powdered cork or adsorbent 20 carbon black; water-soluble polymers, resins, waxes; or solid fertilizers. Such composition may, if so desired, contain one or more compatible agents such as wetting agents, dispersing agents, emulsifiers or colourings which, when they are solid, may also act as diluents. The fillers may also be liquid, for example: water, alcohols, in particular butanol or glycol, as well as ethers or esters thereof, in particular methyl glycol acetate; ketones, in particular acetone, 25 cyclohexanone, methyl ethyl ketone, methyl isobutyl ketone or isophorone; petroleum fractions such as paraffinic or aromatic hydrocarbons, in particular xylenes or alkylnaphthalenes; mineral or plant oils; aliphatic chlorohydrocarbons, in particular trichloroethane or methylene chloride; aromatic chlorohydrocarbons, in particular chlorobenzenes; water-soluble or highly polar solvents such as dimethylformamide, dimethyl sulphoxide, N,N-dimethyl-acetamide or N 30 methylpyrrolidone; N-octylpyrrolidone, liquefied gases; or the like, whether they are taken separately or as a mixture. The surfactant can be an emulsifier, a dispersing agent or a wetting agent, of ionic or nonionic type or a mixture of these surfactants. Among those surfactants there are used, for example, polyacrylic acid salts, lignosulphonic acid salts, phenolsulphonic or naphthalenesulphonic acid 35 salts, polycondensates of ethylene oxide with fatty alcohols or fatty acids or fatty esters or fatty 4212713_1 (GHMatters) P80785.AU.1 15 amines, substituted phenols (in particular alkylphenols or arylphenols), ester-salts of sulphosuccinic acid, taurine derivatives (in particular alkyl taurates), phosphoric esters of alcohols or of polycondensates of ethylene oxide with phenols, fatty acid esters with polyols, or sulphate, sulphonate or phosphate functional derivatives of the compounds described above. 5 The presence of at least one surfactant is generally essential when the active ingredients and/or the inert filler are insoluble or only sparingly soluble in water and when the filler for the said composition to be applied is water. The formulations may also contain other additives such as adhesives or dyes. Adhesives such as carboxymethylcellulose or natural or synthetic polymers in the form of powders, granules or 10 matrices, such as gum arabic, latex, polyvinylpyrrolidone, polyvinyl alcohol or polyvinyl acetate, natural phospholipids, such as cephalins or lecithins, or synthetic phospholipids can be used in the formulations. It is possible to use colourings such as inorganic pigments, such as, for example: iron oxides, titanium oxides, Prussian blue; organic colouring stuffs, such as those of the alizarin, azo or metal phthalocyanin type; or of trace elements such as iron, manganese, 15 boron, copper, cobalt, molybdenum or zinc salts. The form of the pesticide composition according to the invention can be selected in a large number of formulations, such as aerosol dispenser; suspension of capsules; cold fogging concentrate; dustable powder; emulsifiable concentrate; aqueous/aqueous type emulsion; 20 oil/inverse type emulsion; encapsulated granule; fine granule; suspension concentrate for seed treatment; compressed gas; gas generating product; granule; hot fogging concentrate; macrogranule; microgranule; oil-dispersible powder; oil miscible suspension concentrate; oil miscible liquid; paste; plant rodlet; powder for dry seed treatment; seeds coated with a pesticide; smoke maydle; smoke cartridge; smoke generator; smoke pellet; smoke rodlet; 25 smoke tablet; smoke tin; soluble concentrate; soluble powder; solution for seed treatment; suspension concentrate (= flowable concentrate); ultra low volume liquid; ultra low volume suspension; vapour releasing product; water-dispersible granules or tablets; water dispersible powder for slurry treatment; water-soluble granules or tablets; water-soluble powder for seed treatment; wettable powder. 30 The pesticide composition according to the present invention covers not only the compositions which are ready to be applied to the crop by means of a suitable device, such as a spraying device, but also the commercial concentrated composition which have to be diluted before application to the crop. 42127131 (GHMatters) P80785.AU.1 16 The pesticide composition herein described is used in general for application to growing plants, or to sites where crops are grown or intended to grow, or for the treatment, coating or film coating of seeds. According to the present invention, seeds may comprise any propagation materials, like for 5 example seeds, fruit, tubers, grains, roots, rhizomes, parts of plants. The pesticide composition according to the invention may also be applied to the vegetation and in particular to the leaves infested or capable of being infested with the phytopathogenic fungi or damaged by insects. Another method of applying the pesticide composition according to the invention is to add a formulation containing the active ingredients to the irrigation water. 10 According to another object of the present invention, there is provided a method for controlling the phytopathogenic fungi or damaging insects of plants, crops or seeds, characterized in that an agronomically effective and substantially non-phytotoxic quantity of a pesticide composition according to the invention is applied as seed treatment, foliar application, stem application, 15 drench or drip application or chemigation to the seed, the plant or to the fruit of the plant or to soil or to inert substrate (e.g. inorganic substrates like sand, rockwool, glasswool; expanded minerals like perlite, vermiculite, zeolite or expanded clay), Pumice, Pyroclastic materials or stuff, synthetic organic substrates (e.g. polyurethane), organic substrates (e.g. peat, composts, tree waste products like coir, wood fibre or chips, tree bark) or to a liquid substrate (e.g. floating 20 hydroponic systems, Nutrient Film Technique, Aeroponics) wherein the plant is growing or in which it is desired to grow. The expression "are applied to the plants to be treated" is understood to mean, for the purposes of the present invention, that the pesticide composition which is the subject of the invention can be applied by means of various methods of treatment such as: 25 - spraying onto the aerial parts of the said plants a liquid comprising one of the said compositions, - dusting, the incorporation into the soil of granules or powders, spraying, around the said plants, and in the case of trees injection or daubing, - coating or film-coating the seeds of the said plants with the aid of a plant-protection 30 mixture comprising one of the said compositions. The method according to the invention may either be a curing, preventing or eradicating method. In this method, a composition used can be prepared beforehand by mixing the two or more active compounds according to the invention. 42127131 (GHMatters) P80785.AU.1 17 According to an alternative of such a method, it is also possible to apply simultaneously, successively or separately compounds (A) and (B) and optionally (C) so as to have the conjugated (A)/(B) (optionally (C)) effects, of distinct compositions each containing one of the two or three active ingredients (A) or (B), optionally (C). Such a method can be extended to the 5 further application of compound (C). The dose of active compound usually applied in the method of treatment according to the invention is generally and advantageously - for foliar treatments: from 0.1 to 10,000 g/ha, preferably from 10 to 1,000 g/ha, 10 more preferably from 50 to 300g/ha; in case of drench or drip application, the dose can even be reduced, especially while using inert substrates like rockwool or perlite; - for seed treatment: from 2 to 200 g per 100 kilogram of seed, preferably from 3 to 150 g per 100 kilogram of seed; - for soil treatment: from 0.1 to 10,000 g/ha, preferably from Ito 5,000 g/ha. 15 The doses herein indicated are given as illustrative examples of the method according to the invention. A person skilled in the art will know how to adapt the application doses, notably according to the nature of the plant or crop to be treated. Under specific conditions, for example according to the nature of the phytopathogenic fungus to be treated or insect to control, a lower dose may offer adequate protection. Certain climatic 20 conditions, resistance or other factors like the nature of the phytopathogenic fungi or damaging insect to be eliminated or the degree of infestation, for example, of the plants with these fungi, may require higher doses of combined active ingredients. The optimum dose usually depends on several factors, for example on the type of phytopathogenic fungus to be treated or insect to control, on the type or level of development of 25 the infested plant, on the density of vegetation, or alternatively on the method of application. Without it being limiting, the crop treated with the pesticide composition or combination according to the invention is, for example, grapevine, but this could be cereals, vegetables, lucerne, soybean, market garden crops, turf, wood, tree or horticultural plants. 30 The method of treatment according to the invention may also be useful to treat propagation material such as tubers or rhizomes, but also seeds, seedlings or seedlings pricking out and plants or plants pricking out. This method of treatment may also be useful to treat roots. The method of treatment according to the invention may also be useful to treat the over-ground parts of the plant such as trunks, stems or stalks, leaves, flowers and fruit of the concerned plant. 42127131 (GHMatters) P80785.AU.1 18 Among the plants that can be protected by the method according to the invention, mention can be made of cotton; flax; vine; fruit or vegetable crops such as Rosaceae sp. (for instance pip fruit such as apples and pears, but also stone fruit such as apricots, almonds and peaches), Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., 5 Moraceae sp., Oleaceae sp., Actinidaceae sp., Lauraceae sp., Musaceae sp. (for instance banana trees and plantins), Rubiaceae sp., Theaceae sp., Sterculiceae sp., Rutaceae sp. (for instance lemons, oranges and grapefruit); Solanaceae sp. (for instance tomatoes), Liliaceae sp., Asteraceae sp. (for instance lettuces), Umbelliferae sp., Cruciferae sp., Chenopodiaceae sp., Cucurbitaceae sp., Papilionaceae sp. (for instance peas), Rosaceae sp. (for instance 10 strawberries); major crops such as Graminae sp. (for instance maize, lawn or cereals such as wheat, rice, barley and triticale), Asteraceae sp. (for instance sunflower), Cruciferae sp. (for instance colza), Fabacae sp. (for instance peanuts), Papilionaceae sp. (for instance soybean), Solanaceae sp. (for instance potatoes), Chenopodiaceae sp. (for instance beetroots); horticultural and forest crops; as well as genetically modified homologues of these crops. 15 The composition according to the invention may also be used in the treatment of genetically modified organisms with the compounds according to the invention or the agrochemical compositions according to the invention. Genetically modified plants are plants into genome of which a heterologous gene encoding a protein of interest has been stably integrated. The 20 expression "heterologous gene encoding a protein of interest" essentially means genes which give the transformed plant new agronomic properties, or genes for improving the agronomic quality of the modified plant. The composition according to the invention may also be used against fungal diseases liable to 25 grow on or inside timber. The term "timber" means all types of species of wood, and all types of working of this wood intended for construction, for example solid wood, high-density wood, laminated wood, and plywood. The method for treating timber according to the invention mainly consists in contacting one or more compounds according to the invention, or a composition according to the invention; this includes for example direct application, spraying, dipping, 30 injection or any other suitable means. Among the diseases of plants or crops that can be controlled by the method according to the invention, mention can be made of: Powdery mildew diseases such as: 35 Blumeria diseases, caused for example by Blumeria graminis; 42127131 (GHMatters) P80785,AU.1 19 Podosphaera diseases, caused for example by Podosphaera leucotricha; Sphaerotheca diseases, caused for example by Sphaerotheca fuliginea; Uncinula diseases, caused for example by Uncinula necator; Rust diseases such as: 5 Gymnosporangium diseases, caused for example by Gymnosporangium sabinae; Hemileia diseases, caused for example by Hemileia vastatrix; Phakopsora diseases, caused for example by Phakopsora pachyrhizi or Phakopsora meibomiae; Puccinia diseases, caused for example by Puccinia recondita; 10 Uromyces diseases, caused for example by Uromyces appendiculatus; Oomycete diseases such as: Bremia diseases, caused for example by Bremia lactucae; Peronospora diseases, caused for example by Peronospora pisi or P. brassicae; Phytophthora diseases, caused for example by Phytophthora infestans; 15 Plasmopara diseases, caused for example by Plasmopara viticola; Pseudoperonospora diseases, caused for example by Pseudoperonospora humuli or Pseudoperonospora cubensis; Pythium diseases, caused for example by Pythium ultimum; Leafspot, leaf blotch and leaf blight diseases such as : 20 Alternaria diseases, caused for example by Alternaria solani; Cercospora diseases, caused for example by Cercospora beticola; Cladiosporum diseases, caused for example by Cladiosporium cucumerinum; Cochliobolus diseases, caused for example by Cochliobolus sativus; Colletotrichum diseases, caused for example by Colletotrichum lindemuthanium; 25 Cycloconium diseases, caused for example by Cycloconium oleaginum; Diaporthe diseases, caused for example by Diaporthe citri; Elsinoe diseases, caused for example by Elsinoe fawcettii; Gloeosporium diseases, caused for example by Gloeosporium laeticolor; Glomerella diseases, caused for example by Glomerella cingulata; 30 Guignardia diseases, caused for example by Guignardia bidwelli; Leptosphaeria diseases, caused for example by Leptosphaeria maculans Leptosphaeria nodorum; Magnaporthe diseases, caused for example by Magnaporthe grisea; Mycosphaerella diseases, caused for example by Mycosphaerella graminicola 35 Mycosphaerella arachidicola; Mycosphaerella fiiensis; 4212713_1 (GHMatters) P80785.AU.1 20 Phaeosphaeria diseases, caused for example by Phaeosphaeria nodorum; Pyrenophora diseases, caused for example by Pyrenophora teres; Ramularia diseases, caused for example by Ramularia collo-cygni; Rhynchosporium diseases, caused for example by Rhynchosporium secalis; 5 Septoria diseases, caused for example by Septoria apii or Septoria lycopercisi; Typhula diseases, caused for example by Typhula incarnata; Venturia diseases, caused for example by Venturia inaequalis; Root and stem diseases such as: Corticium diseases, caused for example by Corticium graminearum; 10 Fusarium diseases, caused for example by Fusarium oxysporum; Gaeumannomyces diseases, caused for example by Gaeumannomyces graminis; Rhizoctonia diseases, caused for example by Rhizoctonia solani; Tapesia diseases, caused for example by Tapesia acuformis; Thielaviopsis diseases, caused for example by Thielaviopsis basicola; 15 Ear and panicle diseases such as: Alternaria diseases, caused for example by Alternaria spp.; Aspergillus diseases, caused for example by Aspergillus flavus; Cladosporium diseases, caused for example by Cladosporium spp.; Claviceps diseases, caused for example by Claviceps purpurea ; 20 Fusarium diseases, caused for example by Fusarium culmorum; Gibberella diseases, caused for example by Gibberella zeae; Monographella diseases, caused for example by Monographella nivalis; Smut and bunt diseases such as: Sphacelotheca diseases, caused for example by Sphacelotheca reillana; 25 Tilletia diseases, caused for example by Tilletia caries; Urocystis diseases, caused for example by Urocystis occulta; Ustilago diseases, caused for example by Ustilago nuda; Fruit rot and mould diseases such as: Aspergillus diseases, caused for example by Aspergillus flavus; 30 Botrytis diseases, caused for example by Botrytis cinerea ; Penicillium diseases, caused for example by Penicillium expansum; Sclerotinia diseases, caused for example by Sclerotinia sclerotiorum; Verticilium diseases, caused for example by Verticilium alboatrum; Seed and soilborne decay, mould, wilt, rot and damping-off diseases: 35 Fusarium diseases, caused for example by Fusarium culmorum; 4212713_1 (GHMatters) P80785.AU.1 21 Phytophthora diseases, caused for example by Phytophthora cactorum; Pythium diseases, caused for example by Pythium ultimum; Rhizoctonia diseases, caused for example by Rhizoctonia solani; Sclerotium diseases, caused for example by Sclerotium rolfsii; 5 Microdochium diseases, caused for example by Microdochium nivale; Canker, broom and dieback diseases such as: Nectria diseases, caused for example by Nectria galligena; Blight diseases such as: Monilinia diseases, caused for example by Moni/inia laxa; 10 Leaf blister or leaf curl diseases such as : Taphrina diseases, caused for example by Taphrina deformans; Decline diseases of wooden plants such as: Esca diseases, caused for example by Phaemoniella clamydospora; Eutypa dyeback, caused for example by Eutypa lata; 15 Dutch elm disease, caused for example by Ceratocystsc u/mi; Diseases of flowers and Seeds such as: Botrytis diseases, caused for example by Botrytis cinerea; Diseases of tubers such as: Rhizoctonia diseases, caused for example by Rhizoctonia solani 20 Helminthosporium diseases, caused for example by Helminthosporium solani. The damaging insects of crops which can be controlled at any development stage by using the pesticide composition according to the invention include: 0 pests from the order of Isopoda for example Oniscus asellus, Armadi//idium vulgare, 25 Porcellio scaber; 0 pests from the order of Diplopoda for example Blaniulus guttulatus; 0 pests from the order of Chilopoda for example Geophilus carpophagus, Scutigera spp.; 0 pests from the order of Symphyla for example Scutigerella immaculata; 0 pests from the order of Thysanura for example Lepisma saccharina; 30 e pests from the order of Collembola for example Onychiurus armatus; * pests from the order of Orthoptera for example Acheta domesticus, Gryllota/pa spp., Locusta migratoria migratorioides, Melanop/us spp., Schistocerca gregaria; 0 pests from the order of Blattaria for example Blatta orientalis, Periplaneta americana, Leucophaea maderae, Blattella germanica; 35 * pests from the order of Dermaptera for example Forficula auricularia; 42127131 (GHMatters) P80785.AU.1 22 " pests from the order of Isoptera for example Reticulitermes spp.; * pests from the order of Phthiraptera for example Pediculus humanus corporis, Haematopinus spp., Linognathus spp., Trichodectes spp., Damalinia spp.; " pests from the order of Thysanoptera for example Hercinothrips femoralis, Thrips 5 tabaci, Thrips palm, Frankliniella accidentalis; * pests from the order of Heteroptera for example Eurygaster spp., Dysdercus intermedius, Piesma quadrata, Cimex lectularius, Rhodnius prolixus, Triatoma spp; " pests from the order of Homoptera for example Aleurodes brassicae, Bemisia tabaci, Trialeurodes vaporariorum, Aphis gossypii, Brevicoryne brassicae, Cryptomyzus ribis, 10 Aphis fabae, Aphis pomi, Eriosoma lanigerum, Hyalopterus arundinis, Phylloxera vastatrix, Pemphigus spp., Macrosiphum avenae, Myzus spp., Phorodon humuli, Rhopalosiphum padi, Empoasca spp., Euscelis bilobatus, Nephotettix cincticeps, Lecanium corni, Saissetia oleae, Laodelphax striatellus, Nilaparvata lugens, Aonidiella aurantii, Aspidiotus hederae, Pseudococcus spp., Psylla spp; 15 e pests from the order of Lepidoptera for example Pectinophora gossypiella, Bupalus piniarius, Cheimatobia brumata, Lithocolletis blancardella, Hyponomeuta padella, Plutella xylostella, Malacosoma neustria, Euproctis chrysorrhoea, Lymantria spp., Bucculatrix thurberiella, Phyllocnistis citrella, Agrotis spp., Euxoa spp., Feltia spp., Earias insulana, Heliothis spp., Mamestra brassicae, Panolis flammea, Spodoptera 20 spp., Trichoplusia ni, Carpocapsa pomonella, Pieris spp., Chilo spp., Pyrausta nubilalis, Ephestia kuehniella, Galleria mellonella, Tineola bisselliella, Tinea pellionella, Hofmannophila pseudospretella, Cacoecia podana, Capua reticulana, Choristoneura fumiferana, Clysia ambiguella, Homona magnanima, Tortrix viridana, Cnaphalocerus spp., Oulema oryzae; 25 e pests from the order of Coleoptera for example Anobium punctatum, Rhizopertha dominica, Bruchidius obtectus, Acanthoscelides obtectus, Hylotrupes bajulus, Agelastica alni, Leptinotarsa decemlineata, Phaedon cochleariae, Diabrotica spp., Psylliodes chrysocephala, Epilachna varivestis, Atomaria spp., Oryzaephilus surinamensis, Anthonomus spp., Sitophilus spp., Otiorrhynchus sulcatus, Cosmopolites 30 sordidus, Ceuthorrhynchus assimilis, Hypera postica, Dermestes spp., Trogoderma spp., Anthrenus spp., Attagenus spp., Lyctus spp., Meligethes aeneus, Ptinus spp., Niptus hololeucus, Gibbium psylloides, Tribolium spp., Tenebrio molitor, Agriotes spp., Conoderus spp., Melolontha melolontha, Amphimallon solstitialis, Costelytra zealandica, Lissorhoptrus oryzophilus; 4212713_1 (GHMatters) P80785.AU.1 23 0 pests from the order of Hymenoptera for example Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Vespa spp; e pests from the order of Diptera for example Aedes spp., Anopheles spp., Culex spp., Drosophila melanogaster, Musca spp., Fannia spp., Calliphora erythrocephala, Lucilia 5 spp., Chrysomyia spp., Cuterebra spp., Gastrophilus spp., Hyppobosca spp., Stomoxys spp., Oestrus spp., Hypoderma spp., Tabanus spp., Tannia spp., Bibio hortulanus, Os cinella frit, Phorbia spp., Pegomyia hyoscyami, Ceratitis capitata, Dacus oleae, Tipula paludosa, Hylemyia spp., Liriomyza spp.; 0 pests from the order of Siphonaptera for example Xenopsylla cheopis, Ceratophyllus 10 spp.; * pests from the class of Arachnida for example Scorpio maurus, Latrodectus mactans, Acarus siro, Argas spp., Ornithodoros spp., Dermanyssus gallinae, Eriophyes ribis, Phyllocoptruta oleivora, Boophilus spp., Rhipicephalus spp., Amblyomma spp., Hyalomma spp., Ixodes spp., Psoroptes spp., Chorioptes spp., Sarcoptes spp., Tarso 15 nemus spp., Bryobia praetiosa, Panonychus spp., Tetranychus spp., Hemitarsonemus spp., Brevipalpus spp; e the plant-parasitic neamnotes such as Pratylenchus spp., Radopholus similis, Ditylenchus dipsaci, Tylenchulus semipenetrans, Heterodera spp., Globodera spp., Meloidogyne spp., Aphelenchoides spp., Longidorus spp., Xiphinema spp., Trichodorus 20 spp., Bursaphelenchus spp. As a further aspect, the present invention provides a product comprising a compound (A) and a compound (B) and optionally a compound (C), as herein defined, as a combined preparation for simultaneous, separate or sequential use in controlling the phytopathogenic fungi or damaging 25 insects of plants, crops or seeds at a site. The pesticide composition according to the invention can be prepared immediately before use by using a kit-of-parts for controlling, curatively or preventively, the phytopathogenic fungi of crops, such a kit-of-parts may comprise at least one compound (A) and at least one compound (B) and optionally compound (C) intended to be combined or used simultaneously, separately or 30 sequentially in controlling the phytopathogenic fungi of crops at a site. It is therefore a pack in which the user finds all the ingredients for preparing the fungicide formulation which they wish to apply to the crops. These ingredients, which comprise in particular the active agents (A) and (B) and optionally compound (C) and which are packaged separately, are provided in the form of a powder or in the form of a liquid which is concentrated 35 to a greater or lesser degree. The user simply has to mix in the prescribed doses and to add the 4212713_1 (GHMatters) P80785.AU.1 24 quantities of liquid, for example of water, necessary to obtain a formulation which is ready to use and which can be applied to the crops. The present invention can be illustrated by the following and non-limitative examples. 5 Efficacy example A: Plutella xylostella test Solvent: 7 parts by weight of dimethylformamide Emulsifier: 2 parts by weight of alkylaryl polyglycolether To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with 10 emulsifier-containing water to the desired concentration. Cabbage leaves (Brassica oleracea) are treated by being dipped into the preparation of the active compound at the desired concentration and are infested with larvae of the diamond black moth Plute//a xylostella as long as the leaves are still moist. After a period of time of 4 days, the mortality is determined. 100% means that all the caterpillars 15 have been killed; 0 % means that none of the caterpillars have been killed. According to the present application in this test e.g. the following combination shows a synergistic effect in comparison to the single compounds. The results are presented in table 1. Rate of application of Expected value active compound (ppm) Efficacy according to (%) Colby formula (%) propamocarb 200 25 / thiacloprid 20 20 / propamocarb + thiacloprid 200 + 20 80 40 Table 1 Efficacy example B: Spodoptera exigua test 20 Solvent: 7 parts by weight of dimethylformamide Emulsifier: 2 parts by weight of alkylaryl polyglycolether To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration. 25 Cabbage leaves (Brassica oleracea) are treated by being dipped into the preparation of the active compound at the desired concentration and are infested with larvae of the beet army worm (Spodoptera exigua) as long as the leaves are still moist. After a period of time of 6 days, the mortality is determined. 100% means that all the caterpillars have been killed; 0 % means that none of the caterpillars have been killed. 4212713_1 (GHMatters) P80785.AU.1 25 According to the present application in this test e.g. the following combination shows a synergistic effect in comparison to the single compounds. The results are presented in table 2. Rate of application of Expected value active compound (ppm) Efficacy according to (%) Colby formula (%) propamocarb 100 0 / clothianidin 100 45 / propamocarb + clothianidin 100 + 100 100 45 Table 2 5 Efficacy example C : Spodoptera frugiperda test Solvent: 7 parts by weight of dimethylformamide Emulsifier: 2 parts by weight of alkylaryl polyglycolether To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with 10 emulsifier-containing water to the desired concentration. Cabbage leaves (Brassica oleracea) are treated by being dipped into the preparation of the active compound at the desired concentration and are infested with larvae of the fall army worm (Spodoptera frugiperda) as long as the leaves are still moist. After a period of time of 4 days, the mortality is determined. 100% means that all the caterpillars 15 have been killed; 0 % means that none of the caterpillars have been killed. According to the present application in this test e.g. the following combination shows a synergistic effect in comparison to the single compounds. The results are presented in table 3. Rate of application of Efficacy Expected value active compound (%) according to (ppm) Colby formula (%) propamocarb 100 0 / propamocarb 200 0 / clothianidin 20 0 / imidacloprid 20 0 / thiamethoxam 100 0 / propamocarb + clothianidin 100 + 20 20 0 propamocarb + imidacloprid 200 + 20 40 0 propamocarb + thiamethoxam 200 + 100 80 0 Table 3 4212713_1 (GHMatters) P80785.AU.1 26 Example 1: Myzus persicae - test Solvent: 78.0 parts by weight acetone 1.5 parts by weight dimethylformamide 5 Emulsifier: 0.5 parts by weight alkylarylpolyglycolether To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration. Chinese cabbage (Brassica pekinensis) leaf- disks infected with all instars of the green peach 10 aphid (Myzus persicae), are sprayed with a preparation of the active ingredient of the desired concentration. After the specified period of time, mortality in % is determined. 100 % means that all aphids have been killed; 0 % means that none of the aphids have been killed. The mortality values determined thus are recalculated using the Colby-formula. 15 According to the present application in this test e.g. the following combination shows a synergistic effect in comparison to the single compounds: Table 4: Myzus persicae - test Active ingredient Concentration Mortality in % after 6 d g ai/ha Propamocarb-HCl 200 0 Spirodiclofen 20 0 Propamocarb-HCl + Spirodiclofen obs.* cal.** (10 : 1) 200+20 70 0 *obs. = observed insecticidal efficacy, ** cal.= efficacy calculated with Colby-formula 20 42252761 (GHMatters) P80785,AU.1 27 Example 2 Tetranychus urticae - test OP-resistant Solvent: 78.0 parts by weight acetone 1.5 parts by weight dimethylformamide 5 Emulsifier: 0.5 parts by weight alkylarylpolyglycolether To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration. French beans (Phaseolus vulgaris) which are heavily infested with all stages of the two spotted 10 spidermite (Tetranychus urticae), are sprayed with a preparation of the active ingredient of the desired concentration. After the specified period of time, mortality in % is determined. 100% means that all spider mites have been killed and 0% means that none of the spider mites have been killed. The mortality values determined thus are recalculated using the Colby-formula. 15 According to the present application in this test e.g. the following combinations show a synergistic effect in comparison to the single compounds: Table 5: Tetranychus urticae - test OP-resistant Active ingredient Concentration Mortality in % after 6 d g ai/ha Propamocarb-HCl 200 0 Spirodiclofen 100 80 20 80 4 70 0.8 0 Propamocarb-HCl + Spirodiclofen obs.* cal.** (2 : 1) 200+100 100 80 (10 : 1) 200+20 100 80 (50 : 1) 200+4 100 70 (250 : 1) 200+0.8 90 0 *obs. = observed insecticidal efficacy, ** cal.= efficacy calculated with Colby-formula 42252761 (GHMatters) P80785.AU.1 28 Example 3 Phaedon cochleariae larvae - test; spray application Solvent: 7 parts by weight of dimethylformamide Emulsifier: 2 parts by weight of alkylaryl polyglycolether 5 To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration. Ammonium salt and/or penetration enhancer in a dosage of 1000ppm are added to the desired concentration if necessary. Cabbage leaves (Brassica oleracea) are treated by being sprayed with the preparation of the 10 active compound of the desired concentration and are infested with mustard beetle larvae (Phaedon cochleariae). After the specified period of time, mortality in % is determined. 100 % means that all the beetle larvae have been killed; 0 % means that none of the beetle larvae have been killed. The mortality values determined thus are recalculated using the Colby-formula. 15 According to the present application in this test e.g. the following combination shows a synergistic effect in comparison to the single compounds: Table 6: Phaedon cochleariae larvae - test Active ingredient Concentration Mortality in % after 3 d Ppm Propamocarb-HCI 200 0 Spirotetramate 100 10 Propamocarb-HCl + Spirotetramate obs.* cal.** (2 : 1) 200+100 40 10 *obs. = observed insecticidal efficacy, ** cal. = efficacy calculated with Colby-formula 20 42252761 (GHMatters) P80785.AU.1 29 Example 4 Plutella xylostella - test; spray application Solvent: 7 parts by weight of dimethylformamide Emulsifier: 2 parts by weight of alkylaryl polyglycolether 5 To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration. Ammonium salt and/or penetration enhancer in a dosage of 1000ppm are added to the desired concentration if necessary. Cabbage leaves (Brassica oleracea) are treated by being sprayed with the preparation of the 10 active compound of the desired concentration and are infested with larvae of the diamondback moth (Plutella xylostella, sensible strain). After the specified period of time, the mortality in % is determined. 100 % means that all the caterpillars have been killed; 0 % means that none of the caterpillars have been killed. The mortality values determined thus are recalculated using the Colby-formula. 15 According to the present application in this test e.g. the following combination shows a synergistic effect in comparison to the single compounds: Table 7: Plutella xylostella - test Active ingredient Concentration Mortality in % after 2 d ppm Propamocarb-HCl 200 0 Spirotetramate 100 10 Propamocarb-HCI + Spirotetramate obs.* cal.** (2 : 1) 200+ 100 45 10 *obs. = observed insecticidal efficacy, ** cal. = efficacy calculated with Colby-formula 20 42252761 (GHMatters) P80785.AU.1 30 Example 5 Spodoptera frugiperda - test; spray application Solvent: 7 parts by weight of dimethylformamide Emulsifier: 2 parts by weight of alkylaryl polyglycolether 5 To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration. Ammonium salt and/or penetration enhancer in a dosage of 1000ppm are added to the desired concentration if necessary. Cotton leaves (Gossypium hirsutum) are treated by being sprayed with the preparation of the 10 active compound of the desired concentration and are infested with caterpillars of the fall army worm (Spodopterafrugiperda). After the specified period of time, mortality in % is determined. 100 % means that all the caterpillars have been killed; 0 % means that none of the caterpillars have been killed. The mortality values determined thus are recalculated using the Colby-formula. 15 According to the present application in this test e.g. the following combination shows a synergistic effect in comparison to the single compounds: Table 8: Spodoptera frugiperda - test Active ingredient Concentration Mortality in % after 1d ppm Propamocarb-HCl 100 0 Rynaxypyr 4 50 Propamocarb-HCl + Rynaxypyr obs.* cal.** (25 : 1) 100+4 70 50 *obs. = observed insecticidal efficacy, ** cal. = efficacy calculated with Colby-formula 20 42252761 (GHMatters) P80785.AU.1 3 0a Also described herein are the following items Ito 13: 1. A composition comprising: A) propamocarb-HCI and 5 B) an insecticide compound in an A/B weight ratio ranging from 1/1,000 to 1,000/1; provided that insecticide compound B differs from compounds of formula (1) Hal OH2 * S0 2 CH 3 N H R H

/CF

3 N F CF OP413

H

3 C (1) 10 wherein - Hal represents a chlorine atom, a bromine atom or a iodine atom; - R represents hydrogen or methyl and * may represent a carbon atom in R- or S configuration. 15 2. A composition according to item 1 wherein compound B is selected in the list consisting of abamectin, acephate, acetamiprid, acrinathrin, aldicarb, alpha-cypermethrin, beta cyfluthrin, bifenthrin, carbaryl, carbofuran, chlorfenapyr, chlorfluazuron, chlorpyrifos-E, clothianidin, cyfluthrin, cypermethrin, cyromazine, deltamethrin, diflubenzuron, dinotefuran, emamectin-benzoate, ethiprole, fenpyroximate, fipronil, flonicamid, flubendiamide, flufenoxuron, 20 gamma-cyhalothrin, hexaflumuron, imidacloprid, indoxacarb, L-cyhalothrin, lepimectin, lufenuron, methamidophos, methiocarb, methomyl, methoxyfenozide, milbemycin, nitenpyram, novaluron, profenofos, pymetrozine, rynaxapyr, spinosad, spirodiclofen, spiromesifen, spirotetramate, tebufenozide, tebufenozide, tebufenpyrad, tebufenpyrad, tebupirimphos, teflubenzuron, tefluthrin, thiacloprid, thiamethoxam, thiodicarb, triazophos triflumuron, 25 imidaclothiz and (2E)-1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3,5-dimethyl-N-nitro-1,3,5-triazinan-2 imine. 3. A composition according to iterns 1 or 2 wherein compound B is selected in the list consisting of abamectin, acetamiprid, aldicarb, beta-cyfluthrin, carbofuran, chlorpyrifos-E, 30 clothianidin, cypermethrin, cyromazine, deltamethrin, diflubenzuron, emamectin-benzoate, 30b ethiprole, fipronil, gamma-cyhalothrin, imidacloprid, L-cyhalothrin, lufenuron, methiocarb, methoxyfenozide, pymetrozine, rynaxapyr, spinosad, spirodiclofen, spiromesifen, spirotetramate, tebufenozide, tebufenpyrad, tefluthrin, thiacloprid, thiamethoxam, thiodicarb, triflumuron, imidaclothiz and (2E)-1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3,5-dimethyl-N-nitro-1,3,5 5 triazinan-2-imine. 4. A composition according to items 1 to 3 wherein compound B is selected in the list consisting of abamectin, aldicarb, beta-cyfluthrin, chlorpyrifos-E, clothianidin, cyromazine, deltamethrin, diflubenzuron, emamectin-benzoate, fipronil, gamma-cyhalothrin, imidacloprid, L 10 cyhalothrin, methiocarb, pymetrozine, rynaxapyr, spinosad, spirodiclofen, spiromesifen, spirotetramate, tebufenozide, tebufenpyrad, tefluthrin, thiamethoxam, thiodicarb, imidaclothiz, (2E)-1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3,5-dimethyl-N-nitro-1,3,5-triazinan-2-imine. 5. A composition according to items 1 to 4 wherein the A/B weight ratio ranges from 15 1/125 to 125/1. 6. A composition according to items 1 to 5 wherein the A/B weight ratio ranges from 1/25 to 25/1. 20 7. A composition according to items 1 to 6 further comprising C) a further fungicide compound in an A/B/C weight ratio ranging from 1/1,000/1,000 to 1/0.001/0.001. 8. A composition according to item 7 wherein compound C is selected in the list consisting of benalaxyl, benalaxyl-M, benthiavalicarb, carboxin, chlorothalonil, cyazofamid, 25 cymoxanil, dimetomorph, fluazinam, fludioxonil, fluoxastrobin, fluquinconazole, flutriafol, fosetyl Al, hexaconazole, hymexazol, ipconazole, mancozeb, mandipropamid, maneb, mefenoxam, metalaxyl, metiram, penconazole, penthiopyrad, phosphorous acid, propamocarb-fosetylate, propineb, prothioconazole, tebuconazole, thiram, triadimenol, trifloxystrobin, triticonazole and N [2-(1,3-dimethyl-butyl)-phenyl]-5-fluoro-1,3-dimethyl-1 H-pyrazole-4-carboxamide. 30 9. A composition according to items 7 or 8 wherein the A/B/C weight ratio ranges from 1/100/100 to 1/0.01/0.01. 10. A composition according to items 7 to 9 wherein the A/B/C weight ratio ranges from 35 1/80/80 to 1/0.05/0.05 30c 11. A composition according to items 7 to 10 wherein the A/B/C weight ratio ranges from 1/50/100 to 1/1.5/2.5. 5 12. A composition according to items 7 to 11 wherein the A/B/C weight ratio ranges from 1/12/25 to 1/6/12. 13. A method for controlling the phytopathogenic fungi or damaging insects of plants, crops or seeds comprising the application of an agronomically effective and substantially non-phytotoxic 10 quantity of a pesticide composition according to items 1 to 12 as seed treatment, foliar application, stem application, drench or drip application or chemigation to the seed, the plant or to the fruit of the plant or to soil or to inert substrate, Pumice, Pyroclastic materials or stuff, synthetic organic substrates, organic substrates or to a liquid substrate wherein the plant is growing or in which it is desired to grow. 15

Claims (13)

1. A composition comprising: A) propamocarb-HCI and 5 B) an insecticide compound selected from the group consisting of spirodiclofen, spiromesifen, spirotetramat, and rynaxypyr in an A/B weight ratio ranging from 1/1,000 to 1,000/1.

2. A composition according to claim 1 wherein compound B is selected from the group 10 consisting of spiromesifen and spirotetramate.

3. A composition according to claim 1 or 2 wherein compound B is selected from the group consisting of spirotetramate. 15

4. A composition according to claim 1 wherein compound B is rynaxypyr.

5 A composition according to claims 1 to 4 wherein the A/B weight ratio ranges from 1/125 to 125/1. 20

6. A composition according to claims 1 to 5 wherein the A/B weight ratio ranges from 1/25 to 25/1.

7. A composition according to claims 1 to 6 further comprising C) a further fungicide compound in an A/B/C weight ratio ranging from 1/1,000/1,000 to 1/0.001/0.001. 25

8. A composition according to claim 7 wherein compound C is selected in the list consisting of benalaxyl, benalaxyl-M, benthiavalicarb, carboxin, chlorothalonil, cyazofamid, cymoxanil, dimetomorph, fluazinam, fludioxonil, fluoxastrobin, fluquinconazole, flutriafol, fosetyl Al, hexaconazole, hymexazol, ipconazole, mancozeb, mandipropamid, maneb, mefenoxam, 30 metalaxyl, metiram, penconazole, penthiopyrad, phosphorous acid, propamocarb-fosetylate, propineb, prothioconazole, tebuconazole, thiram, triadimenol, trifloxystrobin, triticonazole and N [2-(1,3-dimethyl-butyl)-phenyl]-5-fluoro-1,3-dimethyl-1 H-pyrazole-4-carboxamide.

9, A composition according to claims 7 or 8 wherein the A/B/C weight ratio ranges from 35 1/100/100 to 1/0.01/0.01. 42127131 (GHMatters) P80785.AU.1 32

10. A composition according to claims 7 to 9 wherein the A/B/C weight ratio ranges from 1/80/80 to 1/0.05/0.05 5

11. A composition according to claims 7 to 10 wherein the A/B/C weight ratio ranges from 1/50/100 to 1/1.5/2.5.

12. A composition according to claims 7 to 11 wherein the A/B/C weight ratio ranges from 1/12/25 to 1/6/12. 10

13. A method for controlling the phytopathogenic fungi or damaging insects of plants, crops or seeds comprising the application of an agronomically effective and substantially non phytotoxic quantity of a pesticide composition according to claims 1 to 12 as seed treatment, foliar application, stem application, drench or drip application or chemigation to the seed, the 15 plant or to the fruit of the plant or to soil or to inert substrate, Pumice, Pyroclastic materials or stuff, synthetic organic substrates, organic substrates or to a liquid substrate wherein the plant is growing or in which it is desired to grow. 4212713_1 (GHMatters) P80785.AU.1