Title of Invention

INSECTICIDAL MIXTURE CONTAINING GAMMA - CYHALOTHRIN

Abstract

An insecticidal composition comprising gamma-cyhalothrin and one or more further active ingredients having insecticidal, nematicidal or acaricidal activity wherein the further active ingredient is one or more of thiamethoxam, abamectin, emamectin benzoate, spinosad, chlorpyrifos, chlorpyrifos-methyl, profenofos, lufenuron, indoxacarb, lambda-cyhalothrin, pymetrozine, methidathion, imidacloprid, acetamiprid, thiacloprid, fipronil, methoxyfenozide, chlorfenapyr, pyridaben, novaluron, pyridalyl and piperonyl butoxide, an insecticidally inert carrier or diluent and, optionally, one or more surface active agents, wherein the ingredients gamma-cyhalothrin and second insecticide are present in the ratio 1:100 to 100:1 weight/weight.

Full Text

FORM 2 THE PATENTS ACT, 1970 [39 OF 1970] COMPLETE SPECIFICATION [See Section 10; Rule 13] "INSECTICIDAL COMPOSITION COMPRISING GAMMA-CYHALOTHRIN" SYNGENTA LIMITED, a British company of European Regional Centre, Priestley Road, Surry Research Park, Guildford, Surrey GU27YH, England, The following specification particularly describes the nature of the invention and the manner in which it is to be performed:- GRANTED 12-5-2006 3 0 MAR 2006 This invention relates to mixtures with insecticidal properties comprising two or more active ingredients, to compositions containing them and to methods of controlling unwanted pests using such mixtures or compositions. More particularly, the invention relates to mixtures containing garnma-cyhalothrin [(S)-a-cyano-3-phenoxybenzyl (Z)-(lR,3R)-3-(2-chloro-3,3,3-trifluoro-l-propenyl)-2,2-dimethylcyclopropanecarboxylate] and another compound having insecticidal, nematicidal, acaricidal, molluscicidal, fungicidal, plant growth regulating or herbicidal activity, to compositions containing the mixture and to insecticidal methods using such mixtures or compositions. Compounds having insecticidal, nematicidal, acaricidal, molluscicidal, fungicidal, plant growth regulating or herbicidal activity are hereinafter referred to as active ingredients. (S)-a-Cyano-3-phenoxybenzyl(Z)-(lR,3R)-3-(2-chloro-3,3,3-trifluoro-l-propenyl)-2,2-dimethylcyclopropanecarboxylate and its insecticidal activity was disclosed by Bentley et al, Pestic. Sci. (1980), 11(2), 156-64. Combining garnma-cyhalothrin and one or more further active ingredients can provide useful biological effects such as synergy against important pests such as Heliothis virescens, Spodoptera littoralis and Myzus persicae. There is therefore provided a mixture of garnma-cyhalothrin and one or more further active ingredients. It is preferred that the further active ingredient, other than garnma-cyhalothrin is an active ingredient having insecticidal, nematicidal or acaricidal activity. Examples of suitable insecticides that may be used as a further active ingredient in the mixture of the invention may be any compound selected from: a) Pyrethroids, such as permethrin, cypermethrin, fenvalerate, esfenvalerate, deltamethrin, cyhalothrin (in particular lambda-cyhalothrin), bifenthrin, fenpropathrin, cyfluthrin, tefluthrin, fish safe pyrethroids (for example ethofenprox), natural pyrethrin, tetramethrin, s bioallethrin, fenfluthrin, prallethrin or 5 benzyl-3-furylmethyl-(E)-(1R,3S)-2,2-dimethyl- 3-(2-oxothiolan-3-ylidenemethyl)cyclopropane carboxylate or any of their insecticidally active isomers; b) Organophosphates, such as, methidathion, chlorpyrifos-methyl, profenofos, sulprofos, acephate, methyl parathion, azinphos-methyl, demeton-s-methyl, heptenophos, thiometon, fenamiphos, monocrotophos, profenofos, triazophos, methamidophos, dimethoate, buprofezin) for use in rice may be employed. Alternatively insecticides or acaricides specific for particular insect species/stages may also be included in the mixtures (for example acaricidal ovo-larvicides, such as clofentezine, flubenzimine, hexythiazox or tetradifon; acaricidal motilicides, such as dicofol or propargite; acaricides, such as acequinocyl, fenazaquin, spirodiclofen, etoxazole, bromopropylate or chlorobenzilate; or growth regulators, such as hydramethylnon, cyromazine, methoprene, chlorfluazuron or diflubenzuron). Examples of suitable insecticide synergists insecticides that may be used as a further active ingredient in the mixture of the invention include piperonyl butoxide, sesamex, safroxan and dodecyl imidazole. The further active ingredient is preferably one or more of thiamethoxam, abamectin, emamectin benzoate, spinosad, chlorpyrifos, chlorpyrifos-methyl, profenofos, lufenuron, indoxacarb, lambda-cyhalothrin, pymetrozine, pirimicarb, methidathion, imidacloprid, acetamiprid, thiacloprid, fipronil, methoxyfenozide, chlorfenapyr, pyridaben, novaluron, pyridalyl, propargite and piperonyl butoxide. The further active ingredient is more preferably one or more of thiacloprid, fipronil, methoxyfenozide, spinosad, profenofos, chlorfenapyr, pyridaben, emamectin benzoate and indoxacarb; or it is one or more of thiamethoxam, abamectin, emamectin benzoate, spinosad, chlorpyrifos, profenofos, lufenuron, indoxacarb and lambda-cyhalothrin. Examples of suitable fungicides that may be used as a further active ingredient in the mixture of the invention may be any compound selected from: (E)-N-methyl-2-[2-(2,5-dimethylphenoxymethyl)phenyl]-2-methoxy-irninoacetamide (SSF-129), 4-bromo-2-cyano-N,N-dimethyl-6-trifluoromemylbenzimidazole-l-sulphonamide, a-[N-(3-chloro-2,6-xylyl)-2-methoxyacetamido]-Y-butyrolactone, 4-chloro-2-cyano-iV,iV-dimethyl-5-p-tolylimidazole-l-sulfonamide (IKF-916, cyamidazosulfamid), 3-5-dichloro-N-(3-chloro-l-ethyl-l-methyl-2-oxopropyl)-4-methylbenzamide (RH-7281, zoxamide),N-allyl-4,5,-dimethyl-2-rrimethylsilylthiophene-3-carboxamide (MON65500),N-(1-cyano-1,2-dimethylpropy)-2-(2,4-dichlorophenoxy)propionamide (AC382042), N-(2-methoxy-5-pyridyl)-cyclopropane carboxamide, acibenzolar (CGA245704), alanycarb, aldimorph, anilazine, azaconazole, azoxystrobin, benalaxyl, benomyl, biloxazol, bitertanol, blasticidin S, bromuconazole, bupirimate, captafol, captan, carbendazim, carbendazim chlorhydrate, carboxin, carpropamid, carvone, CGA41396, CGA41397, chinomethionate, chlorothalonil, chlorozolinate, clozylacon, copper containing D. amide herbicides such as benfluamid, bromobutide, carbetamide, flufenacet, isoxaben, naproanilide, napropamide, naptalam, propyzamide and tebutam E. amino acids and salts and esters thereof, such as bialaphos and salts and esters thereof, glufosinate salts and esters thereof, glyphosate and salts and esters thereof, and sulfosate. F. aryloxypropionates, including the optically active isomers thereof, such as clodinafop-propargyl, cyhalofop-butyl, diclofop & esters thereof eg methyl ester, fenoxaprop & esters thereof eg ethyl ester, fluazifop-butyl, haloxyfop and esters thereof, propaquizafop, quizalofop and esters thereof and quizalofop-p-tefuryl G. arylanilides such as diflufenican, flamprop, flamprop-M and esters thereof H. arylureas such as chlorbromuron, chlorotoluron, daimuron (dymron), dimefuron, diuron, fenuron, fluometuron, isoproturon, isouron, linuron, methabenzthiazuron, methyldymron, metobromuron, metoxuron, monolinuron, neburon and tebuthiuron I. benzo-2,l,3-thiadiazin-4-one-dioxides such as bentazone J. benzoic acids such as 2,3,6-trichlorobenzoic acid, chloramben and dicamba K. bipyridyliums such as diquat and salts thereof, and paraquat and salts thereof. L. carbamates such as chlorpropham and propham, and phenylcarbamoyloxyphenyl carbamates such as desmedipham and phenmedipham. M. acetamides such as acetochlor, alachlor, butachlor, dimethachlor, dimethenamid and isomers thereof, metazachlor, metolachlor and isomers thereof, pretilachlor, propachlor, propisochlor and thenylchlor. N. cyclohexanediones such as alloxydim and salts thereof, butroxydim, clethodim, cycloxydim, sethoxydim, tepraloxydim and tralkoxydim. O. dihalobenzonitriles such as dichlobenil P. dinitrophenols such as dinoterb and dintro ortho-cresol (DNOC) Q. diphenyl ethers such as aciflurofen and salts and esters thereof, aclonifen, bifenox, chlomethoxyfen, chlornitrofen, fluroglycofen or salts or ester thereof, fomesafen, lactofen and oxyflnorfen. R. dinitraanilines such as dinitramine, ethalfluralin, fluchloralin, oryzalin, pendimethalin, prodiamine and trifluralin. S. haloalkanoic herbicides such as dalapon and trichloroacetic acid and salts thereof . T. hydroxybenzonitrile (HBN) herbicides such as bromoxynil and ioxynil, and HBN precursors such as bromofenoxim n. sulfonylureas such as amidosulfuron, azimsulfuron, bensulfuron and esters thereof, chlorimuron & esters eg ethyl ester thereof, chlorsulfuron, cinosulfuron, ethametsulfuron-methyl, flazasulfuron, flupyrsulfuron and salts thereof, halosulfuron-methyl, ethoxysulfuron, imazosulfuron, iodosulfuron, metsulfuron and esters thereof, nicosulfuron, oxasulfuron, primisulfuron & esters eg methyl ester thereof, prosulfuron, pyrazosulfuron-ethyl, rimsulfuron, sulfometuron-methyl, sulfosulfuron, thifensulfuron-methyl, triasulfuron, tribenuron, tribenuron-methyl and triflusulfuron-methyl JJ. thiocarbamates such as butylate, cycloate, dimepiperate, S-ethyl dipropylthiocarbamate (EPTC), esprocarb, molinate, orbencarb, pebulate, prosulfocarb, thiobencarb, tiocarbazil, tri-allate and vernolate. KK. triazine herbicides such as ametryn, atrazine, cyanazine, dimethametryn, prometon, prometryn, propazine, simazine, simetryn, terbuthylazine, terbutryn and trietazine. LL. triazole herbicides such as amitrole. MM. triazolinones such as carfentrazone-ethyl and sulfentrazone. NN. triketones such as sulcotrione and mesotrione. OO. uracils such as bromacil, lenacil and terbacil. Examples of suitable plant growth regulators that may be used as a further active ingredient in the mixture of the invention may be any compound selected from ancymidol, chlormequat chloride, ethephon, flumetralin, flurprimidol, gibberellic acid, gibberellin A4/gibberellin A7, maleic hydrazide, mepiquat chloride, paclobutrazol, prohexadione calcium, thiadiazuron, trinexapac ethyl and uniconazole. In order to apply the active ingredients to a pest, a locus of pest, or to a plant susceptible to attack by a pest, or, as a fungicide to a plant, to a seed of a plant, to the locus of the plant or seed, to soil or to any other growth medium, the active ingredients are usually formulated into a composition which includes, in addition to the active ingredients, a suitable inert diluent or carrier and, optionally, a surface active agent (SFA). SFAs are chemicals which are able to.modify the.properties of an. interface (for example, liquid/solid, liquid/air or liquid/liquid interfaces) by lowering the interfacial tension and thereby leading to changes in other properties (for example dispersion, emulsification and wetting). In one particular aspect the present invention merefore also provides novel insecticidal compositions comprising gamma cyhalothrin and one or more compounds possessing insecticidal, nematicidal, acaricidal, molluscicidal, fungicidal, plant growth said agents to improve water dispersibility/solubility. The mixture is then ground to a fine powder. Similar compositions may also be granulated to form water soluble granules (SG). Wettable powders (WP) may be prepared by mixing the active ingredients with one or more solid diluents or carriers, one or more wetting agents and, preferably, one or more dispersing agents and, optionally, one or more suspending agents to facilitate the dispersion in liquids. The mixture is then ground to a fine powder. Similar compositions may also be granulated to form water dispersible granules (WG). Granules (GR) may be formed either by granulating a mixture of the active ingredients and one or more powdered solid diluents or carriers, or from pre-formed blank granules by absorbing the active ingredients (or a solution thereof, in a suitable agent) in a porous granular material (such as pumice, attapulgite clays, fuller's earth, kieselguhr, diatomaceous earths or ground corn cobs) or by adsorbing the active ingredients (or a solution thereof, in a suitable agent) on to a hard core material (such as sands, silicates, mineral carbonates, sulphates or phosphates) and drying if necessary. Agents which are commonly used to aid absorption or adsorption include solvents (such as aliphatic and aromatic petroleum solvents, alcohols, ethers, ketones and esters) and sticking agents (such as polyvinyl acetates, polyvinyl alcohols, dextrins, sugars and vegetable oils). One or more other additives may also be included in granules (for example an emulsifying agent, wetting agent or dispersing agent). Dispersible Concentrates (DC) may be prepared by dissolving the active ingredients in water or an organic solvent, such as a ketone, alcohol or glycol ether. These solutions may contain a surface active agent (for example to improve water dilution or prevent crystallisation in a spray tank). Emulsifiable concentrates (EC) or oil-in-water emulsions (EW) may be prepared by dissolving the active ingredients in an organic solvent (optionally containing one or more wetting agents, one or more emulsifying agents or a mixture of said agents). Suitable organic solvents for use in ECs include aromatic hydrocarbons (such as alkylbenzenes or alkylnaphthalenes; exemplified byS0LVESSO-1O0; SOLVESSG 150 and SOLVES SO 200; SOLVESSO is a Registered Trade Mark), ketones (such as cyclohexanone or methylcyclohexanone) and alcohols (such as benzyl alcohol, furfuryl alcohol or butanol), N-alkylpyrrolidones (such as N-methylpyrrolidone or N-octylpyrrolidone), dimethyl amides of fatty acids (such as C8-C10 fatty acid dimethyl amide) and chlorinated hydrocarbons. An EC product may spontaneously emulsify on addition to water, to produce an emulsion with Capsule suspensions (CS) may be prepared in a manner similar to the preparation of EW formulations but with an additional polymerisation stage such that an aqueous dispersion of oil droplets is obtained, in which each oil droplet is encapsulated by a polymeric shell and contains the active ingredients and, optionally, a carrier or diluent therefor. The polymeric shell may be produced by either an interfacial polycondensation reaction or by a coacervation procedure. The compositions may provide for controlled release of the active ingredients and they may be used for seed treatment, the active ingredients may also be formulated in a biodegradable polymeric matrix to provide a slow, controlled release of the compound. A composition may include one or more additives to improve the biological performance of the composition (for example by improving wetting, retention or distribution on surfaces; resistance to rain on treated surfaces; or uptake or mobility of the active ingredients). Such additives include surface active agents, spray additives based on oils, for example certain mineral oils or natural plant oils (such as soy bean and rape seed oil), and blends of these with other bio-enhancing adjuvants (ingredients which may aid or modify the action of the active ingredients. The active ingredients may also be formulated for use as a seed treatment, for example as a powder composition, including a powder for dry seed treatment (DS), a water soluble powder (SS) or a water dispersible powder for slurry treatment (WS), or as a liquid composition, including a flowable concentrate (FS), a solution (LS) or a capsule suspension (CS). The preparations of DS, SS, WS, FS and LS compositions are very similar to those of, respectively, DP, SP, WP, SC and DC compositions described above. Compositions for treating seed may include an agent for assisting the adhesion of the composition to the seed (for example a mineral oil or a film-forming barrier). Wetting agents, dispersing agents and emulsifying agents may be surface SFAs of the cationic, anionic, amphoteric or non-ionic type. Suitable SFAs of the cationic type include quaternary ammonium compounds (for example cetyltrimethyl ammonium bromide), imidazolines and amine salts. Suitable anionic SFAs include alkali metals salts of fatty acids, salts of aliphatic monoesters of sulphuric acid (for example sodium lauryl sulphate), salts of sulphonated aromatic compounds (for example sodium dodecylbenzenesulphonate, calcium dodecylbenzenesulphonate, butylnaphthalene sulphonate and mixtures of sodium di-isopropyl- and tri-wopropyl-naphthalene sulphonates), ether sulphates, alcohol ether sulphates (for example sodium laureth-3-sulphate), ether carboxylates (for example sodium The active ingredients may also be injected into plants or sprayed onto vegetation using electrodynamic spraying techniques or other low volume methods, or applied by land or aerial irrigation systems. Compositions for use as aqueous preparations (aqueous solutions or dispersions) are generally supplied in the form of a concentrate containing a high proportion of the active ingredient, the concentrate being added to water before use. These concentrates, which may include DCs, SCs, ECs, EWs, MEs SGs, SPs, WPs, WGs and CSs, are often required to withstand storage for prolonged periods and, after such storage, to be capable of addition to water to form aqueous preparations which remain homogeneous for a sufficient time to enable them to be applied by conventional spray equipment. Such aqueous preparations may contain varying amounts of the active ingredients (for example 0.0001 to 10%, by weight) depending upon the purpose for which they are to be used. The active ingredients may be used in mixtures with fertilisers (for example nitrogen-, potassium- or phosphorus-containing fertilisers). Suitable formulation types include granules of fertiliser. The mixtures suitably contain up to 25% by weight of the active ingredients. The invention therefore also provides a fertiliser composition comprising a fertiliser and the active ingredients. The amount of composition of the present invention generally applied for the control of insect pests gives a rate of active ingredient from 0.01 to 10 kg per hectare, preferably from 0.1 to 6 kg per hectare. The mixture of the invention is preferably presented in a single composition. However the components may be presented in separate containers, one containing gamma-cyhalothrin optionally in combination with a solid or liquid diluent, and the second containing a further active ingredient optionally in combination with a solid or liquid diluent. Alternatively the components may be presented in a two pack-container, one compartment of which contains gamma-cyhalothrin optionally in combination with a solid or liquid diluent and a second compartment which contains a further active ingredient optionally in combination with a solid or liquid diluent The contents of the two containers or the two compartments can then be admixed, for example by mixing both in water prior to administration. In another aspect the present invention provides a method of combating insect, acarine or nematode include insect pests such as Lepidoptera, Diptera, Homoptera and Coleoptera (including Diabrotica, that is, com rootworm), pests associated with agriculture (American dog tick), Ctenocephalides felis (cat flea), Liriomyza spp. (leafminer), Musca domestica (housefly), Aedes aegypti (mosquito), Anopheles spp. (mosquitoes), Culex spp. (mosquitoes), Lucillia spp. (blowflies), Blattella germanica (cockroach), Periplaneta americana (cockroach), Blatta orientalis (cockroach), termites of the Mastotermitidae (for i example Mastotermes spp.), the Kalotermitidae (for example Neotennes spp.), the Rhinotermitidae (for example Coptotermes formosanus, Reticulitermes flavipes, R. speratu, R. virginicus, R. hespents, and R. santonensis) and the Termitidae (for example Globitermes sulphureus), Solenopsis geminata (fire ant), Monomorium pharaonis (pharaoh's ant), Damalinia spp. and Linognathus spp. (biting and sucking lice), Meloidogyne spp. (root knot nematodes), Globodera spp. and Heterodera spp. (cyst nematodes), Pratylenchus spp. (lesion nematodes), Rhodopholus spp. (banana burrowing nematodes), Tylenchulus spp.(citrus nematodes), Haemonchus contortus (barber pole wonn), Caenorhabditis elegans (vinegar eelworm), Trichostrongylus spp. (gastro intestinal nematodes) and Deroceras reticulatum (slug). The invention therefore provides a method of combating and controlling insects, acarines, nematodes or molluscs which comprises applying an insecticidally, acaricidally, nematicidally or molluscicidally effective amount of a mixture containing gamma-cyhalothrin and one or more compounds possessing insecticidal, nematicidal, acaricidal, molluscicidal, fungicidal, plant growth regulating or herbicidal activity to a pest, a locus of pest, or to a plant susceptible to attack by a pest, to a seed of a plant, to the locus of the plant or seed, to soil or to any other growth medium (for example a nutrient solution). The term "plant" as used herein includes seedlings, bushes and trees. Furthermore, the fungicidal method of the invention includes protectant, curative, systemic, eradicant and antisporulant treatments. The invention is illustrated by the following Examples. EXAMPLE 1 Test compositions were made up from technical active ingredient in 0.05% Synperonic NP8 with the exception of spinosad, for which Tracer 480SC diluted in water was used. For Heliothis and Spodoptera testing cotton leaves were sprayed in a Berkhard Potter Tower, left to dry for 1 hour and then placed on the top of pots containing twenty 1st instar Heliothis virescens/Spodoptera littoralis larvae. These were stored in a test holding room at 25°C for 3 days and the test species assessed for mortality. For aphid testing Leaf TABLE I Results for test using Heliothis virescens TABLE II Results for test using Spodoptera littoralis WE CLAIM: 1. An insecticidal composition comprising gamma-cyhalothrin and one or more further active ingredients having insecticidal, nematicidal or acaricidal activity wherein the further active ingredient is one or more of thiamethoxam, abamectin, emamectin benzoate, spinosad, chlorpyrifos, chlorpyrifos-methyl, profenofos, lufenuron, indoxacarb, lambda-cyhalothrin, pymetrozine, methidathion, imidacloprid, acetamiprid, thiacloprid, fipronil, methoxyfenozide, chlorfenapyr, pyridaben, novaluron, pyridalyl and piperonyl butoxide, an insecticidally inert carrier or diluent and, optionally, one or more surface active agents, wherein the ingredients gamma-cyhalothrin and second insecticide are present in the ratio 1:100 to 100:1 weight/weight. 2. A method of combating and controlling insect, acarine or nematode pests at a locus which comprises treating the pests or the locus of the pests with an insecticidal compostion as claimed in claim 1 comprising gamma-cyhalothrin and one or more further active ingredients having insecticidal, nematicidal or acaricidal activity wherein the further active ingredient is one or more of thiamethoxam, abamectin, emamectin benzoate, spinosad, chlorpyrifos, chlorpyrifos-methyl, profenofos, lufenuron, indoxacarb, lambda-cyhalothrin, pymetrozine, methidathion, imidacloprid, acetamiprid, thiacloprid, fipronil, methoxyfenozide, chlorfenapyr, pyridaben, novaluron, pyridalyl and piperonyl butoxide, 3. A method as claimed in claim 2 wherein the pests are insect pests of growing plants. Dated this 7th day of January, 2004. [RITUSHKA NEGI] OF REMFRY & SAGAR ATTORNEY FOR THE APPLICANT[S]

Documents:

14-mumnp-2004-abstract(6-9-2007).pdf

14-mumnp-2004-cancelled pages(12-5-2006).pdf

14-mumnp-2004-claims(6-9-2007).pdf

14-MUMNP-2004-CLAIMS(8-1-2004).pdf

14-MUMNP-2004-CLAIMS(AMENDED)-(12-5-2006).pdf

14-mumnp-2004-correspondence(12-5-2006).pdf

14-MUMNP-2004-CORRESPONDENCE(IPO)-(15-10-2007).pdf

14-mumnp-2004-correspondence(ipo)-(18-9-2006).pdf

14-MUMNP-2004-DESCRIPTION(COMPLETE)-(8-1-2004).pdf

14-mumnp-2004-description(granted)-(6-9-2007).pdf

14-MUMNP-2004-FORM 1(8-1-2004).pdf

14-mumnp-2004-form 18(10-6-2005).pdf

14-mumnp-2004-form 1a(8-1-2004).pdf

14-MUMNP-2004-FORM 2(COMPLETE)-(8-1-2004).pdf

14-mumnp-2004-form 2(granted)-(6-9-2007).pdf

14-mumnp-2004-form 2(title page)-(6-9-2007).pdf

14-MUMNP-2004-FORM 2(TITLE PAGE)-(COMPLETE)-(8-1-2004).pdf

14-MUMNP-2004-FORM 2(TITLE PAGE)-(GRANTED)-(6-9-2007).pdf

14-mumnp-2004-form 3(30-12-2004).pdf

14-mumnp-2004-form 3(30-3-2004).pdf

14-mumnp-2004-form 3(30-3-2006).pdf

14-MUMNP-2004-FORM 3(8-1-2004).pdf

14-mumnp-2004-form 4(10-5-2006).pdf

14-MUMNP-2004-FORM 4(12-5-2006).pdf

14-mumnp-2004-form 5(30-3-2006).pdf

14-MUMNP-2004-FORM 5(8-1-2004).pdf

14-mumnp-2004-form-pct-ipea-409(8-1-2004).pdf

14-mumnp-2004-form-pct-isa-210(8-1-2004).pdf

14-mumnp-2004-petition under rule 137(31-3-2006).pdf

14-mumnp-2004-petition under rule 138(31-3-2004).pdf

14-MUMNP-2004-PETITION UNDER RULE 138(31-3-2006).pdf

14-mumnp-2004-power of authority(12-5-2006).pdf

14-MUMNP-2004-POWER OF AUTHORITY(8-1-2004).pdf

14-MUMNP-2004-SPECIFICATION(AMENDED)-(30-3-2006).pdf

14-MUMNP-2004-WO INTERNATIONAL PUBLICATION REPORT(8-1-2004).pdf