Stable agrochemical composition and process thereof

10660337 ยท 2020-05-26

Assignee

Inventors

Cpc classification

International classification

Abstract

An agrochemical composition comprising at least one low melting active ingredient; at least one moisture sensitive active ingredient; and an additive, characterised in that said additive has a softening point or melting point lower than the melting point of said low melting active ingredient; a process for the preparation thereof, a method of use thereof and a kit comprising the same is disclosed.

Claims

1. An agrochemical composition comprising: a) about 0.1% w/w to about 30% w/w of bifenthrin; b) about 0.5% w/w to about 95% w/w of at least one moisture sensitive active ingredient selected from the group consisting of acephate, azinphos-methyl, carbofuran, chlorpyrifos, coumaphos, crufomate, dimethoate, ethoprop, famphur, fenamiphos, isofenfos, methamidophos, methidathion, methyl parathion, mevinphos, monocrotophos, metam sodium, phosalone, phosmet, phosphamidon, profenofos, TEPP, terbufos, tetrachlorvinphos, trichlorfon and combinations thereof; and c) about 1% w/w to about 30% w/w of an additive selected from the group consisting of polyethylene glycol (PEG) 6000, PEG 4000 and PEG 8000.

2. The composition according to claim 1, wherein said at least one moisture sensitive active ingredient is acephate.

3. The composition according to claim 2, wherein the composition comprises: a) about 1.0% w/w to about 20% w/w of bifenthrin; b) about 5.0% w/w to about 80% w/w of acephate; and c) about 5.0% to about 20% w/w of PEG 6000.

4. The composition according to claim 1, wherein the composition is a Dry Flowable (DF) formulation.

5. A kit comprising: a) about 0.1% w/w to about 30% w/w of bifenthrin; b) about 0.5% w/w to about 95% w/w of at least one moisture sensitive active ingredient selected from the group consisting of acephate, azinphos-methyl, carbofuran, chlorpyrifos, coumaphos, crufomate, dimethoate, ethoprop, famphur, fenamiphos, isofenfos, methamidophos, methidathion, methyl parathion, mevinphos, monocrotophos, metam sodium, phosalone, phosmet, phosphamidon, profenofos, TEPP, terbufos, tetrachlorvinphos, trichlorfon and combinations thereof; and c) about 1% w/w to about 30% w/w of an additive selected from the group consisting of polyethylene glycol (PEG) 6000, PEG 4000 and PEG 8000.

6. The kit according to claim 4, wherein said at least one moisture sensitive active ingredient is acephate.

7. The kit according to claim 5, wherein the kit comprises: a) about 1.0% w/w to about 20% w/w of bifenthrin; b) about 5.0% w/w to about 80% w/w of acephate; and c) about 5.0% to about 20% w/w of PEG 6000.

Description

DETAILED DESCRIPTION OF THE INVENTION

(1) Inventors of the present invention have surprisingly found that a stable agrochemical composition in the form a granular composition of a low melting active ingredient and a moisture sensitive active ingredient can be prepared by mixing the low melting active ingredient with a moisture sensitive active ingredient in the presence of an additive and exposing the pre-mix to compact granulation.

(2) It has been found out surprisingly that the additive used by the inventors prevents the low melting active ingredient from undergoing crystal modifications or forming a crust on the granules. It is indeed surprising that the additive of the present invention allows the storage of the product under any conditions and still maintain the quality of the product without any deterioration in the dispersibility, suspensibility and availability of the active.

(3) It is an accepted method to test the formulation for long term stability and performance to allow the formulation to be kept at 54 degrees for 14 days called as accelerated heat stability (AHS) test and then test the dispersibility, suspensibility and wet sieve test. Drop in suspensibility and dispersibility indicate the poor performance of the formulation in the field after long term storage and increase in wet sieve test indicate the formation of large particles which in the field will clog the nozzle.

(4) It is observed by the inventors that the formulation of the present invention passes all the tests after AHS thereby proving its effectiveness in the field even after long term storage. It is believed that the additive used during the process enables the formulation to remain stable for longer duration on storage.

(5) As used herein the term composition is used interchangeably with the term formulation and is intended to refer to the stable solid dry flowable intended to prevent damage of agricultural crops and its produce from insects and pests.

(6) Compounds are referred to herein as low melting active ingredient, which is a term recognized in the relevant art, particularly in the field of agrochemical compositions. In particular, a low melting active compound according to the present invention is a compound that has a melting point of less than about 100 C., less than about 90 C., less than about 85 C., less than about 80 C., less than about 75 C., or less than about 70 C. or having ability to solidify on room temperature. In certain embodiments, a low melting compound according to the invention is a compound with a melting point in the range of about 20 C. to about 100 C. In specific embodiments, a low melting compound is a compound that has a melting point in the range of about 25 C. to about 100 C., about 30 C. to about 100 C., about 30 C. to about 90 C., about 30 C. to about 80 C., about 30 C. to about 70 C., about 40 C. to about 90 C., about 40 C. to about 80 C., about 50 C. to about 90 C., about 50 C. to about 80 C., or about 50 C. to about 70 C.

(7) The term moisture sensitive active ingredient refers to a compound having ability to absorb moisture and undergoes degradation or other changes in physico-chemical parameters.

(8) As used herein, the term compaction granulation denotes a process of granulation wherein compositions comprising active ingredients is separately, sequentially or simultaneously subjected to compaction by applying pressure as well as to granulation by suitable mechanism such as extrusion.

(9) As used herein, the term degradation denotes loss of the active ingredient as a result of exposure to moisture/or on storage.

(10) The term softening point denotes the temperature at which the additive reaches a specific degree of softness. The softening point is close to but lower than the melting point of the additive.

(11) The term locus as used herein refers to a place to which a combination according to the invention is applied. It includes application to an individual plant, a group of plants such as a plant and/or its surrounding, and the region in which plants may be planted as well application directly to an insect or insects and/or the vicinity in which they are located.

(12) The term agrochemical in the context of this invention refers to any agent used to destroy insects, arachnids, fungi, unwanted vegetation, rodents, and other pests.

(13) The term insects includes all organisms in the class Insecta. Insecticidal refers to the ability of a substance to increase mortality or inhibit, growth rate of insects.

(14) The term plants refers to all physical parts of a plant, including seeds, seedlings, saplings, roots, tubers, stems, stalks, foliage and fruits.

(15) The term agrochemically effective amount of active refers to an amount of an active that kills or inhibits the plant disease for which control is desired, in an amount not significantly toxic to the plant being treated.

(16) To control or controlling insects means to inhibit, through a toxic effect, the ability of insect pests to survive, grow, feed, and/or reproduce, or to limit insect-related damage or loss in crop plants. To control insects may or may not mean killing the insects, although it preferably means killing the insects.

(17) The inventors of the present invention have found that the addition of an additive to a composition of a moisture sensitive active ingredient, preferably an organophosphorus insecticide, and a low melting active ingredient resulted in highly stable compositions. The stable composition achieved by addition of an additive facilitated granule formation in the absence of water. Thus, the present invention provides for compositions that allows avoiding the use of water.

(18) Without wishing to be bound by theory, the inventors in the present invention have surprisingly found, that addition of a low softening or low melting additive to a combination of low melting active ingredient such as pyrethroids and moisture sensitive active ingredients such as organophosphorus insecticide results in stable granular compositions.

(19) Dry flowables or granules of the present invention are easy to prepare and store, have good dispersibility and suspensibility under storage conditions. The use of an additive in obtaining said stable insecticidal composition without water, circumvents moisture responsible for degradation of moisture sensitive active like acephate, and compaction below melting point of low-melting pyrethroids (i.e. 30-58 degree Celsius) avoids the cementing problem that occurs due to melting and gradual cooling during temperature variation in the process and on storage.

(20) Thus, in an aspect, the present invention may provide a stable agrochemical composition comprising: a) at least one low melting active ingredient; b) at least one moisture sensitive active ingredient; and c) an additive;
characterised in that said additive has a softening point or melting point lower than the melting point of the low melting active ingredient.

(21) In another aspect, the present invention may provide a stable insecticidal composition comprising: a) at least one low melting pyrethroid; b) at least one moisture sensitive insecticide; and c) an additive;
characterised in that said additive has a softening point or melting point lower than the melting point of the low melting pyrethroid.

(22) In an embodiment, the low melting active ingredient of the present invention may be selected from insecticides, attractants, sterilants, bactericides, acaracides, nematicides, fungicides, growth regulators, herbicides, fertilizers and mixtures.

(23) In a preferred embodiment, the low melting active ingredient of the present invention is selected from insecticides, attractants, sterilants, bactericides, acaracides, nematicides, fungicides and growth regulators.

(24) In an embodiment the low melting active ingredient of the present invention is selected from nitrothal-isopropyl, myclobutanil, piproctanyl bromide, jodfenphos, Imazalil, lambda-cyhalthrin, triflumizole, vamidothion, xylylcarb, tolclofos-methyl, prothoate, pyriproxyfen, propamocarb hydrochloride, tefluthrin, resmethrin, chlorpropham, cloethocarb, demeton-S, cyfluthrin, cypermethrin, azinphos-ethyl, azinphos-methyl, benalaxyl, benazolin-ethyl, butocarboxim, benzoximate, bioresmethrin, bromopropylate, borax, biphenyl, fluoroglycofen-ethyl, fenbucarb, fenthiocarb, fensulfothion, fosmethilan, furalaxyl, dikegulac, trinexapac-ethyl, ethiofencarb, etridiazole, fenamiphos, fenazaquin, EPN, dodemorph, mecarphon, etaconazole, fluorbenside, furmecyclox, fenfluthrin, fluenetil, acequinocyl, schradan, transfluthrin, cyprodinil, phosfolan, crufomate, chlorphoxim, chloropropylate, di-allate, chlorofenprop, camphechlor, chiorbenside, chlordimeform, phosphonic acid, trifloxystrobin, picoxystrobin, gamma-cyhalothrin, codlemone, spinetoram, cyflumetofen.

(25) In an embodiment, the low melting active ingredient of the present invention is selected from strobilurins or pyrethroids.

(26) The low melting pyrethroid may be selected from but not limited to cypermethrin, fenvalerate, permethrin, alphacypermethrin, betacypermethrin, zetacypermethrin, deltamethrin, cyfluthrin, bifenthrin, lambda-cyhalothrin, and/or bioresmethrin or mixtures thereof.

(27) In another preferred embodiment of the present invention, the low melting pyrethroid is selected from bifenthrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, and zeta-cypermethrin.

(28) Thus, in another preferred embodiment, the low melting pyrethroid may be bifenthrin.

(29) In an embodiment, the low melting strobilurin may be selected from trifloxystrobin or picoxystrobin.

(30) In an embodiment, the present invention may provide a stable agrochemical composition comprising from about 0.1% to about 30% w/w and preferably from about 0.2% to about 20% w/w low melting pyrethroid, of the total weight of the stable agrochemical composition.

(31) Another embodiment of the present invention may provide a stable insecticidal composition comprising from about 0.1% to about 30% w/w and preferably from about 0.2% to about 20% w/w low melting pyrethroid, of the total weight of the stable insecticidal composition.

(32) In a preferred embodiment of the present invention, the stable insecticidal composition comprises from about 1% to about 10% w/w low melting pyrethroid, of the total weight of the stable insecticidal composition.

(33) In an embodiment, the moisture sensitive active ingredient present within the compositions may be selected from organophosphorus insecticides.

(34) In an embodiment, the moisture sensitive organophosphorus insecticide may be selected from but not limited to acephate, azinphos-Methyl, carbofuran, chlorpyrifos, coumaphos, crufomate, dimethoate, ethoprop, famphur, fenamiphos, isofenfos, methamidophos, methidathion, methyl parathion, mevinphos, monocrotophos, metam sodium, phosalone, phosmet, phosphamidon, profenofos, TEPP, terbufos, tetrachlorvinphos, trichlorfon and combinations thereof.

(35) The preferred organophosphorus insecticide may be selected from acephate, profenophos, phosphomidon or mixtures thereof.

(36) Accordingly, an embodiment of the present invention may provide a stable insecticidal composition comprising from about 0.5% to about 95% w/w and preferably from about 10% to about 85% w/w organophosphorus insecticide of the total weight of the stable insecticidal composition.

(37) In a preferred embodiment of the present invention, the stable insecticidal composition comprises from about 40% to about 85% w/w organophosphorus insecticide of the total weight of the stable insecticidal composition

(38) In an embodiment, the present invention comprises an additive that has a softening point or melting point lower than the melting point of the low melting active ingredient.

(39) In another embodiment the present invention comprises an additive that has a melting point lower than the melting point of the low melting active ingredient.

(40) In an embodiment the softening point of the additive is lower than its melting point of the low melting active ingredient.

(41) In a preferred embodiment, the present invention comprises an additive that is water soluble.

(42) In an embodiment, the additive of the present invention may be selected from but not limited to polyethylene glycol (PEG) 6000, PEG 4000, PEG 8000, Nonyl phenol 30 EO or high molecular weight ethoxylate or propoxylate of fatty acid, fatty acid alcohol, vegetable oils, polyvinyl alcohols, polyacrylates, starch, carboxymethyl cellulose, alginic acid, agar, gum arabic and xanthan gum.

(43) In another embodiment, the additive of the present invention may be preferably selected from polyethylene glycol (PEG) 6000, PEG 4000, PEG 8000, vegetable oils, and cellulose ethers.

(44) In a preferred embodiment, the additive of the present invention may be selected from polyethylene glycols.

(45) In an embodiment, in the compositions according to the present invention, the additive is present in an amount from about 1% to about 30% by weight of the composition. Preferably the additive is present in an amount from about 3% to about 20% by weight of the formulation.

(46) The stable insecticidal compositions of the present invention may further comprise one or more dispersants, wetting agents, fillers, surfactants, anticaking agents, pH-regulating agents, preservatives, biocides, antifoaming agents, colorants and other formulation aids.

(47) The dispersants may be selected from ionic and nonionic dispersants to enable disintegration of granules in water with ease, such as salts of polystyrene sulphonic acids, salts of polyvinylsuiphonic acids, salts of naphthalenesulphonic acid/formaldehyde condensates, salts of condensates of naphthalenesulphonic acid, phenolsulphonic acid and formaldehyde, and salts of lignosulphonic acid, polyethylene oxide/polypropylene oxide block copolymers, polyethylene glycol ethers of linear alcohols, reaction products of fatty acids with ethylene oxide and/or propylene oxide, furthermore polyvinyl alcohol, polyvinylpyrrolidone, copolymers of polyvinyl alcohol and polyvinylpyrrolidone and copolymers of (meth)acrylic acid and (meth)acrylic esters, furthermore alkyl ethoxylates and alkylarylethoxylates ethoxylated alkylarylphosphated and sulphated ester. The preferred dispersing agents include derivative of ethoxylates of vegetable oil or a mixture of one or more of these; or styrene acrylic polymers or mixtures thereof.

(48) The wetting agents may be selected from soaps; salts of aliphatic monoesters of sulphuric acid including but not limited to sodium lauryl sulphate; sulfoakylamides and salts thereof including but not limited to N-methyl-N-oleoyltaurate Na salt; akylarylsulfonates including but not limited to akylbenzenesulfonates; akylnaphthalenesulfonates and salts thereof and salts of ligninsulfonic acid.

(49) In an embodiment fillers may be selected from insoluble fillers and soluble fillers.

(50) In an embodiment, fillers may be selected preferably from precipitated silica and diatomaceous earth kaolin.

(51) In an embodiment, it is preferred to prepare the insecticidal composition according to the invention as Dry Flowables (DF).

(52) In an embodiment, suitable antifoams may, preferably be, silicones, long-chain alcohols and salts of fatty acids.

(53) Suitable colorants (for example in red, blue and green) are, preferably, pigments, which are sparingly soluble in water, and dyes, which are water-soluble. Examples are inorganic coloring agents (for example iron oxide, titanium oxide, and iron hexacyanoferrate) and organic coloring agents (for example alizarin, azo and phthalocyanin coloring agents).

(54) According to a preferred embodiment, the present invention may provide stable insecticidal compositions comprising acephate, bifenthrin and an additive that has a softening point or melting point lower than the melting point of the low melting active ingredient.

(55) According to specific embodiments a stable insecticidal composition of the present invention may comprise from about 0.5% to about 95% w/w of acephate, from about 0.1% to about 30% w/w of bifenthrin, from about 1.0% to about 30% w/w of an additive that has a softening point or melting point lower than the melting point of the low melting active ingredient.

(56) According to another specific embodiment, a stable insecticidal composition of the present invention may comprise from about 5.0% to about 80% w/w of acephate, from about 1.0% to about 20% w/w of bifenthrin, from about 5.0% to about 20% w/w of PEG 6000 as the additive.

(57) According to an embodiment of the present invention, there is provided a stable agrochemical composition comprising acephate, trifloxystrobin and an additive that has a softening point or melting point lower than the melting point of the low melting active ingredient.

(58) According to specific embodiments a stable agrochemical composition of the present invention may comprise from about 0.5% to about 95% w/w of acephate, from about 0.1% to about 30% w/w of trifloxystrobin, from about 1.0% to about 30% w/w of an additive that has a softening point or melting point lower than the melting point of the low melting active ingredient.

(59) In another embodiment, the present invention provides a process for the preparing a stable agrochemical composition. The process comprises: 1) premixing at least one low melting active ingredient, at least one moisture sensitive active ingredient and an additive wherein the additive has a softening point or melting point lower than the melting point of the low melting active ingredient; and 2) subjecting the premix to compaction granulation.

(60) In an embodiment, the process of the present invention comprises additional conventional steps, which may be necessary but not crucial to achieve the advantages of the present invention.

(61) According to another embodiment of the present invention, in process for preparing the stable agrochemical composition, compaction granulation may take place in such a way that composition may be separately, sequentially or simultaneously subjected to compaction as well as to granulation.

(62) In an embodiment, the present invention provides a process for the preparing a stable agrochemical composition. The process comprises: 1) premixing at least one low melting active ingredient, at least one moisture sensitive active ingredient and an additive wherein the additive has a softening point or melting point lower than the melting point of the low melting active ingredient; and 2) subjecting separately, sequentially or simultaneously, the premix to compaction as well as to granulation.

(63) In a preferred embodiment, the process for preparation of the stable insecticidal composition comprise the following steps: 1) mixing an active ingredient selected from at least one low-melting pyrethroid with required quantity of a precipitated silica to obtain a premix; 2) milling the premix with or without other additives in the air-jet mill to obtain grounded low-melting pyrethroid of desired particle size; 3) adding to the grounded milled low-melting pyrethroid, organophosphorus active ingredient, and an additive wherein the additive has a softening point or melting point lower than the melting point of the low melting active ingredient and any other necessary additive(s) and mixing it to obtain a premix; 4) subjecting the premix to compaction granulation to obtain the granules.

(64) The granules, thus obtained, are preferably tested for required quality specifications. Once the granules pass quality specification, they are preferably filled and packed in desired packing as dry flowables.

(65) The premix of the low melting active ingredient and the moisture sensitive active ingredient and the additive can also be treated by pre-compaction followed by roller extrusion. This premixing of the moisture sensitive active ingredient and low melting active ingredient with the additive prevents the moisture sensitive active ingredient from deteriorating in the composition; and pre-compaction prevents melting of low melting active ingredients during extrusion process.

(66) The composition of the present invention enjoy all the advantages discussed above, making it beneficial from an economic aspect and a handling aspect and shows a very good performance during application. As will be demonstrated in the examples, the composition of the present invention demonstrates good suspensibility, stability, dispersibility, and free flowability and passes the wet sieve test.

(67) According to an embodiment, the present invention provides use of stable agrochemical composition comprising at least one low melting active ingredient, at least one moisture sensitive active ingredient and an additive wherein the additive has a softening point or melting point lower than the melting point of the low melting active ingredient, as an agrochemically active composition.

(68) In an embodiment, the stable compositions according to the present invention are used as insecticides.

(69) Accordingly, the stable insecticidal compositions of the present invention give a quick knockdown kill of the pests. It is especially a potent lethal weapon to kill hard-to-kill, especially Lepidoptera, Coleoptra, Diptera, Hemiptera, preferably, effective against crop insects like leps, stink bug and plant bug.

(70) In an embodiment, the crops on which the compositions of the present invention may be used may be selected from but not limited to cereals, such as wheat, oats, barley, spelt, triticale, rye, maize, millet, rice, crops such as sugarcane, soybean, sunflower, rape, canola, tobacco, sugar beet, fodder beet; tuber crops such as potatoes, sweet potatoes etc., crops such as asparagus, hops etc.; fruit plants such as apples, pears, stone-fruits such as for example peaches, nectarines, cherries, plums, apricots, citrus fruits such as oranges, grapefruit, limes, lemons, kumquats, mandarins, satsumas; nuts such as pistachios, almonds, walnuts, pecan nuts, tropical fruits such as mango, papaya, pineapple, dates, bananas etc., grapes, vegetables such as endives, lambs, lettuce, fennel, globe and loose-leaf salad, chard, spinach, chicory, cauliflower, broccoli, Chinese cabbage, kale (winter kale or curly kale), kohlrabi, Brussel sprouts, red cabbage, white cabbage and savoy, fruiting vegetables such as aubergines, cucumbers, paprika, marrow, tomatoes, courgettes, sweetcorn, root vegetables such as celeriac, turnip, carrots, swedes, radishes, horse radish, beetroot, salsify, celery, pulses such as peas, beans etc., bulb vegetables such as leeks, onions etc., oil crops such as mustard, poppy, olives, sunflowers, coconut, castor oil plants, cocoa beans, groundnuts; fibre crops such as cotton, jute, flex, hemp, crops such as tea, coffee, rubber, ornamentals including shrubs and flowering plants, vines, rangeland and pastures.

(71) In an embodiment, compositions of the present invention may be optionally mixed together with other insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth regulators, herbicides, fertilizers and mixtures thereof.

(72) In an embodiment, the present invention provides a method of controlling unwanted pests, said method comprising applying stable compositions according to the present invention to the pests or to their locus.

(73) Thus, in an embodiment, the present invention may provide methods of controlling insect pests at a locus, said method comprising application of an insecticidally effective amount of a compositions comprising: a) at least one low melting pyrethroid; b) at least one moisture sensitive organophosphorus insecticide; and c) an additive;
characterised in that said additive has a softening point or melting point lower than the melting point of the low melting pyrethroid.

(74) In an embodiment, the present invention may provide methods of controlling insect pest such as those belonging to Lepidopteran, Coleoptran, Dipteran, Hemipteran classes of insecticides.

(75) In another aspect, the present invention provides a kit. The kit comprises a plurality of components, each of which components may include at least one, or more, of the ingredients of the compositions of the present invention.

(76) In an embodiment, the components of the kit may be admixed just prior to being used in any of the methods of use thereof described in this invention.

(77) In an embodiment, the kit comprises an instruction manual that instructs a user of the kit to admix the components in the predefined quantities or in their predefined proportion prior to being used.

(78) In an embodiment, the instruction manual directs the user of the kit to use the composition against predefined insects on certain predefined crops.

(79) Accordingly, in an embodiment, the present invention provides a kit comprising: (a) at least one low melting active ingredient component; (b) at least one moisture sensitive active ingredient component; and (c) an additive component, characterised in that said additive has a softening point or melting point lower than the melting point of said low melting active ingredient.

(80) In another embodiment, the present invention provides a kit comprising: (a) at least one low melting pyrethroid component; (b) at least one moisture sensitive insecticide component; and (c) an additive component, characterised in that said additive has a softening point or melting point lower than the melting point of the low melting pyrethroid.

(81) In an embodiment, the low melting active ingredient component of the present invention comprises strobilurins or pyrethroids.

(82) The low melting pyrethroid may be selected from but not limited to cypermethrin, fenvalerate, permethrin, alphacypermethrin, betacypermethrin, zetacypermethrin, deltamethrin, cyfluthrin, bifenthrin, lambda-cyhalothrin, and/or bioresmethrin or mixtures thereof.

(83) In another preferred embodiment of the present invention, the low melting pyrethroid is selected from bifenthrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, and zeta-cypermethrin.

(84) Thus, in another preferred embodiment, the low melting pyrethroid may be bifenthrin.

(85) In an embodiment, the low melting strobilurin may be selected from trifloxystrobin or picoxystrobin.

(86) In an embodiment, the kit comprises instructions manual instructing the user to use from about 0.1% to about 30% w/w of the low melting pyrethroid component.

(87) In an embodiment, the kit comprises the moisture sensitive active ingredient component selected from organophosphorus insecticides.

(88) In an embodiment, the kit comprises an instruction manual instructing the user to use from about 0.5% to about 95% w/w of the organophosphorus insecticide component.

(89) In an embodiment, the kit comprises an additive component, wherein the additive is selected from polyethylene glycol (PEG) 6000, PEG 4000, PEG 8000, Nonyl phenol 30 EO or high molecular weight ethoxylate or propoxylate of fatty acid, fatty acid alcohol, vegetable oils, polyvinyl alcohols, polyacrylates, starch, carboxymethyl cellulose, alginic acid, agar, gum arabic and xanthan gum.

(90) In an embodiment, the kit comprises an instructions manual instructing the user to mix from about 1% to about 30% of the additive component.

(91) According to a preferred embodiment, the present invention may provide a kit comprising an acephate component, a bifenthrin component and an additive component that has a softening point or melting point lower than the melting point of bifenthrin.

(92) According to another preferred embodiment, the present invention provides a kit comprising an instructions manual instructing the user to admix from about 0.5% to about 95% w/w of the acephate component, from about 0.1% to about 30% w/w of bifenthrin component, and from about 1.0% to about 30% w/w of an additive that has a softening point or melting point lower than the melting point of bifenthrin.

(93) According to another specific embodiment, the present invention provides a kit comprising acephate component instructed to be used from about 5.0% to about 80% w/w, bifenthrin component instructed to be used from about 1.0% to about 20% w/w, and PEG 6000 component instructed to be used from about 5.0% to about 20% w/w.

(94) In an embodiment, the kit comprises acephate component, trifloxystrobin component and an additive component that has a softening point or melting point lower than that of trifloxystrobin.

(95) In an embodiment, the kit comprises instructions for admixing from about 0.5% to about 95% w/w of the acephate component, from about 0.1% to about 30% w/w of trifloxystrobin component, and from about 1.0% to about 30% w/w of the additive component, wherein the additive has a softening point or melting point lower than the melting point of trifloxystrobin.

(96) In an embodiment, the kit comprises instructions for use of the components of kit as insecticide or a fungicide.

(97) In an embodiment, the kit comprises instructions for use of the components against Lepidoptera, Coleoptra, Diptera, Hemiptera, preferably against leps, stink bug and plant bug.

(98) In an embodiment, the kit comprises instructions for use of the components in crops selected from cereals, such as wheat, oats, barley, spelt, triticale, rye, maize, millet, rice, crops such as sugarcane, soybean, sunflower, rape, canola, tobacco, sugar beet, fodder beet; tuber crops such as potatoes, sweet potatoes etc., crops such as asparagus, hops etc.; fruit plants such as apples, pears, stone-fruits such as for example peaches, nectarines, cherries, plums, apricots, citrus fruits such as oranges, grapefruit, limes, lemons, kumquats, mandarins, satsumas; nuts such as pistachios, almonds, walnuts, pecan nuts, tropical fruits such as mango, papaya, pineapple, dates, bananas etc., grapes, vegetables such as endives, lambs, lettuce, fennel, globe and loose-leaf salad, chard, spinach, chicory, cauliflower, broccoli, Chinese cabbage, kale (winter kale or curly kale), kohlrabi, Brussel sprouts, red cabbage, white cabbage and savoy, fruiting vegetables such as aubergines, cucumbers, paprika, marrow, tomatoes, courgettes, sweetcorn, root vegetables such as celeriac, turnip, carrots, swedes, radishes, horse radish, beetroot, salsify, celery, pulses such as peas, beans etc., bulb vegetables such as leeks, onions etc., oil crops such as mustard, poppy, olives, sunflowers, coconut, castor oil plants, cocoa beans, groundnuts; fibre crops such as cotton, jute, flex, hemp, crops such as tea, coffee, rubber, ornamentals including shrubs and flowering plants, vines, rangeland and pastures.

(99) Inventors of the present invention succeeded in preparing stable composition by careful combination of the at least one moisture sensitive active ingredient, at least one low-melting active ingredient and an additive wherein the additive has a softening point or melting point lower than the melting point of the low melting active ingredient and process of preparing the same. The optimum concentration of the actives as well as formulation ingredients which led to the stable DF formulation has been arrived at by the experiments as exemplified below.

(100) These examples are merely illustrations and are not to be understood as limiting the scope and underlying principles of the invention in any way. Indeed, various modifications of the invention in addition to those shown and described herein will become apparent to those skilled in the art from the following examples and foregoing description.

(101) While foregoing written description of the invention enables one of ordinary skill to make and use what is considered presently to be the best mode thereof, those of ordinary skill will understand and appreciate the existence of variations, combinations, and equivalents of the specific embodiment, method, and examples herein. The invention should therefore not be limited by the above described embodiment, method, and examples, but by all embodiments and methods within the scope and spirit of the invention.

EXPERIMENTAL EXAMPLES

(102) The following examples illustrate the basic methodology and versatility of the invention.

Example 1: 74% w/w Acephate and 6% w/w Bifenthrin DF was Prepared as Follows

(103) TABLE-US-00001 Ingredients Quantity (g) Acephate 76.02 Bifenthrin 6.63 Castor oil ethoxylate 4 PEG-6000 11.50 Precipitated silica (PPT silica) 1.85 Total 100.00

(104) Procedure: Bifenthrin technical was mixed with precipitated silica to prepare bifenthrin premix. The bifenthrin premix was milled in airjet mill to obtain desired particle size, Acephate, castor oil ethoxylate, PEG-6000 and precipitated silica were added to the bifenthrin premix to obtain bifenthrin-acephate premix. Bifenthrin-acephate premix was then subjected to compaction granulation by passing said premix through roller extruder to get the granules by multiple passing below melting point of bifenthrin.

Example 2: 74% w/w Acephate and 6% w/w Bifenthrin DF was Prepared a Follows

(105) TABLE-US-00002 Ingredients Quantity (g) Acephate 76.02 Bifenthrin 6.63 Metasperse 550S 3.00 Castor oil ethoxylate 2.5 Dialkyl naphthalene sulphonate 1.00 sodium salt PEG-6000 9.00 PPT silica 1.85 Total 100.00

(106) Procedure: Bifenthrin was mixed with silica to prepare bifenthrin premix. The premix was milled in airjet mill to obtain desired particle size. Acephate, Metasperse 550S, Castor oil ethoxylate, Dialkyl naphthalene sulphonate sodium salt PEG 6000 and precipitated silica were added to the bifenthrin premix to obtain bifenthrin-acephate premix. Bifenthrin-acephate premix was then subjected to compaction granulation by passing said premix through roller extruder to get the granules by multiple passing below melting point of bifenthrin.

Example 3: 74% w/w Acephate and 6% w/w Bifenthrin DF was Prepared as Follows

(107) TABLE-US-00003 Ingredients Quantity (g) Acephate 76.02 Bifenthrin 6.53 Metasperse 550S 3.00 Dialkyl naphthalene sulphonate 1.00 sodium salt PEG-8000 13.10 PPT silica 0.35 Total 100.00

(108) Procedure: Bifenthrin was mixed with silica to prepare bifenthrin premix. The bifenthrin premix was milled in airjet mill to obtain desired particle size. Acephate, Metasperse 550S, Dialkyl naphthalene sulphonate sodium salt, PEG 8000 and precipitated silica were added to the bifenthrin premix to obtain bifenthrin-acephate premix. Bifenthrin-acephate premix was then subjected to compaction granulation by passing said premix through roller extruder to get the granules by multiple passing below melting point of bifenthrin.

Example 4: 74% w/w Acephate and 6% w/w Beta-Cypermethrin DF was Prepared as Follows

(109) TABLE-US-00004 Ingredients Quantity (g) Acephate 76.02 Beta-cypermethrin 6.53 Metasperse 550S 3.00 Dialkyl naphthalene sulphonate 2.00 sodium salt PEG-4000 9.00 Ammonium sulphate 3.10 PPT silica 0.35 Total 100.00

(110) Procedure: Beta-cypermethrin was mixed with silica to prepare beta-cypermethrin premix. The beta-cypermethrin premix was milled in airjet mill to obtain desired particle size. Acephate, Metasperse 550S, Dialkyl naphthalene sulphonate sodium salt, PPT silica, Ammonium Sulphate and PEG 4000 were added to the beta-cypermethrin premix to obtain beta-cypermethrin-acephate premix. Beta-cypermethrin-acephate premix was then subjected to compaction granulation by passing said premix through roller extruder to get the granules by multiple passing below melting point of bifenthrin.

Example 5: 74% w/w Acephate and 6.5% w/w Trifloxystrobin DF was Prepared as Follows

(111) TABLE-US-00005 Ingredients Quantity (g) Acephate 76.02 trifloxystrobin 7.04 Metasperse 550S 3.00 Dialkyl naphthalene sulphonate 2.00 sodium salt PEG-6000 9.00 ammonium sulphate 2.59 PPT silica 0.35 Total 100.00

(112) Procedure: Trifloxystrobin was mixed with silica to prepare Trifloxystrobin premix. The trifloxystrobin premix was milled in airjet mill to obtain desired particle size. Acephate, Metasperse 550S, Dialkyl naphthalene sulphonate sodium salt, PPT silica, ammonium sulphate and PEG 6000 were added to the trifloxystrobin premix to obtain trifloxystrobin-acephate premix. Trifloxystrobin-acephate premix was then subjected to compaction granulation by passing said premix through roller extruder to get the granules.

(113) Stability Data

(114) Test for Dispersibility

(115) Compositions (Examples 6-10) according to the present invention were tested for stability. The samples were prepared using varied quantities of the active ingredients and other ingredients as listed in the below table (Table 1). The samples were prepared as per the process given in Example 1. The samples were tested for dispersibility by observing the number of inversion required to achieve complete dispersion.

(116) TABLE-US-00006 TABLE 1 Exam- Exam- Exam- Exam- Exam- Example Ingredients ple 6 ple 7 ple 8 ple 9 ple 10 11 Acephate 76.02 76.02 76.02 76.02 76.02 76.02 Bifenthrin 6.63 6.53 6.63 6.63 6.63 6.53 Additive* 11.50 13.10 7.50 10.00 3.00 9.00 PPT silica 1.85 0.35 2.85 1.85 3.85 0.35 Castor oil 4.00 2.00 4.5 ethoxylate Soprophor- 3.00 2.00 4D384 Dialkyl 1.00 1.50 1.00 2.00 naphthalene sulphonate sodium salt Metasperse 3.00 3.00 3.00 550S Ammonium 4.0 2.00 3.10 sulfate No. of 15 13 12 13 12 12 Inversions *the additive is selected from PEG 6000, PEG 4000 and PEG 8000

(117) Number of inversion required to achieve complete dispersion of the granules was determined by the following procedure: A graduated cylinder of 250 ml was taken and 2 gm sample was added to the cylinder. It was allowed to soak for 2 min. The graduated cylinder was then closed by putting stopper and tilted to 180 C. and brought back to the original position in 2 seconds.

(118) It was observed that the compositions of the present invention achieved good dispersion in approx. 12-15 inversions and is highly suitable for storage.

(119) Test for Suspensibility and Stability of the Active Ingredient

(120) The DF formulations prepared according to the present invention were investigated for suspensibility, degradation of active ingredient as well as its effect on stability of the composition. Samples (Examples 7 and 11) were prepared as per Example 1.

(121) The samples were kept at 542 C. for up to 14 days and stability parameters such as suspensibility, wet sieve analysis and degradation of active ingredients were tested. The results are summarized in Table 2.

(122) TABLE-US-00007 TABLE 2 Physico/chemical Example 7 Example 11 property 0 days 14 days 0 days 14 days % Acephate 74.35 72.77 74.42 71.55 % Bifenthrin 6.18 6.07 6.22 6.13 Wet sieve analysis 0.02 0.1 0.002 0.003 (retention on 75 test sieve) No. of Inversions 13 13 12 11 Suspensibility 97 95 94 93 Availability of Bifenthrin 5.99 5.77 5.85 5.71

(123) As clear from Table 2, degradation of active acephate and active bifenthrin in DF composition was not observed when kept at of 542 C. for 14 days. There was no significant change in the suspensibility of the formulation, maintaining that the formulations according to the present invention are stable according to the physico-chemical parameters. This signifies that the DF or the granular composition of acephate and bifenthrin so obtained has not only excellent stability of the active ingredients but also retains the dispersibility and hence the availability of the active ingredients for the intended use. It is further established by the result of wet sieve analysis that the crystal modification of bifenthrin has been prevented. The combination of actives and excipients prepared according to the process disclosed in the present invention leads to the stable DF composition which does not undergo any chemical and physical changes on storage and is also easy to handle for further use.

(124) A comparative sample (Example 12) was prepared without the additive of the present invention for comparison purpose. The sample was tested for dispersibility by observing the number of inversion required to achieve complete dispersion.

(125) TABLE-US-00008 Ingredients Example 12 Acephate 76.02 Bifenthrin 6.33 PEG-6000 0.00 PPT silica 1.00 Castor oil ethoxylate 0.00 Soprophor-4D384 Dialkyl naphthalene 2.00 sulphonate sodium salt Metasperse 550S 3.00 Ammonium sulfate 11.65 No. of Inversions >30 Wet sieve analysis (retention 3.52% w/w on 75 test sieve) Suspensibility 45.8% w/w(as bifenthrin) Availability of Bifenthrin 45.8% of total active

(126) It has been observed that the sample (Example 12) prepared without an additive which has a softening point or melting point lower than the melting point of the low melting active ingredient could not provide a good dispersion. Therefore the formulation failed in delivering the required dispersibility and resulted in an unstable formulation.

(127) Test for Availability of Bifenthrin for Insecticidal Activity

(128) The DF formulations prepared according to the present invention were further investigated for finding out the amount of bifenthrin remain available for acting as an insecticide. The suspensibility of a formulation can be directly extrapolated to the active ingredient remain available for the intended use of the active ingredient. Formulations prepared according to the present invention tested for suspensibility in comparison with formulations prepared without additives. The samples were prepared as per example 1 and kept at 542 C. for 14 days and suspensibility was measured.

(129) A review of table 3 given below reveals that, for examples 15-17 prepared according to the present invention, the suspensibility measured was unexpectedly high which obviously indicates that the formulation can be effectively used for the intended insecticidal activity. The % availability of bifenthrin achieved is same as that of the initial concentration of bifenthrin in the formulation. In the case of Examples 13-14 which were prepared without the additive, the measured suspensibility was very low which indicates that the available bifenthrin is only about 50% of what is expected from those formulations.

(130) TABLE-US-00009 TABLE 3 Availability of bifenthrin in the formulations avail- Suspensi- ability of Acephate Bifenthrin Additive* bility of Bifenthrin Examples (g) (g) (g) Bifenthrin (g) Example13 76.0 6.6 0.0 58 3.83 Example14 76.0 6.6 0.0 52 3.43 Example15 76.0 6.6 1.5 95 6.27 Example16 76.0 6.5 12.0 96 6.24 Example17 78.0 5.5 2.5 94 5.17 *the additive is selected from PEG 6000, PEG 4000 and PEG 8000

(131) Inventors of the present invention thus successfully prepared formulation of a low melting active ingredient which is prone to undergo morphological changes along with a moisture sensitive agrochemical. The compositions according to the present invention were found to be stable as well as efficacious for the intended use.