Abstract: TITLE: A NON-AQUEOUS COMPOSITION CONTAINING FLUTHIACET METHYL. ABSTRACT: Synergistic non-aqueous (oil dispersion) agrochemical composition containing Fluthiacet methyl. More particularly the present invention relates to a synergistic Oil Dispersion agrochemical composition comprising bioactive amount of (A) Fluthiacet methyl; (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazoneor their salt; (C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt. The present invention further relates to selection of suitable formulation excipients, process of preparation of the said non-aqueous formulation and its application in the field of agriculture.
DESC:FIELD OF INVENTION:
The present invention relates to a synergistic agrochemical composition. More particularly the present invention relates to a synergistic non-aqueous composition comprising bioactive amount of (A) Fluthiacet methyl (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazone or their salt (C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt.The present invention further relates to selection of suitable formulation excipients, process of preparation of the said non-aqueous formulations and its application in the field of agriculture.
BACKGROUND OF THE INVENTION:
These days cultivation of crops and agriculture in general is cost intensive. Receiving a high yield from the cultivated crops is a key. Hence, to achieve higher yield, protecting crops from pests and diseases and weeds is vital.
Weeds are undesired or unwanted crop or plant which grows sometimes with the essential or desired crop plant and competes with the desired crop plant from an early stage in growth and development. This results in adverse effect on the growth of crop plant and yield.
In earlier days manpower was utilized to remove weeds. Due to research and development in the field of an agriculture now a days chemicals are being used to kill or control the weeds.
It is desirable for the crop protection product to control the harmful plants effectively and, at the same time, to be tolerated by the useful plants in question. Thus, selectivity of the crop protection product is essential to selectively kill the unwanted crops and saves the desired crop in the field.
The control of undesired vegetation is extremely important in order to achieve high crop efficiency. In many cases, herbicides have an effect against a spectrum of weeds; however, these herbicides may not be effective on certain type of other weeds, which may also be present in the crop to be protected. Therefore, there is a strong need for mixing two or more herbicides.
Hence, the most effective way to control weeds is the application of herbicide in accordance with the appropriate management practices with proper formulation thereof.
Treating plants with such a weedicide/herbicide(s) in appropriate formulation helps to control the weeds.
The non-aqueous formulation here in called as oil-based formulation i.e., OD (Oil Dispersion).
In recent years, OD (Oil Dispersion) formulations have been the subject of studies by companies and formulators because of their advantages with respect to the agronomic performance in the field as compared with conventional formulations. Active ingredients (AIs) formulated in different types of formulations usually exhibit different physicochemical characteristics based on type of formulation they are incorporated in. The different performance between them is due to the fact that ODs already contain in their composition oil, such as a mineral or vegetable oil, and emulsifiers, which can act as penetration adjuvants when applied in the field. Penetration adjuvants aid in the absorption of AIs by the plant and, in the case of some conventional formulations, they are used in association with the formulation in the spray mixture, ensuring agronomical effectiveness of the AI. Thus, OD formulations can be deemed “adjuvanted” formulations and do not require additional associated adjuvants to be applied in the field.
Though OD formulation is called as adjuvated formulation it still requires various adjuvants along with formulation excipients. OD formulation presents several challenges in the process of manufacturing and developing stable and effective formulation with choice of proper formulation excipient or adjuvants. To obtain a good and stable formulation over time, optimal formulation additives are required in addition to optimum processes. There were several development and research done in the filed field of formulation development of Oil Dispersion (OD) formulation. Dispersion and activation of active ingredients is the key to the stability of the formulation over time. Solvents or carrier used as a petroleum based or the aromatic solvent, we replaced by the solvents in the form of vegetable oils. Vegetable oils application as a formulation excipient in OD formulation further have their own challenges for stable formulation due to stability issue associated with vegetable oil used and corresponding active ingredient. Although various research has been done in formulation development it has got many draw backs as having high dose of active ingredients and thereby maximizing the pesticidal load into the environment. Many OD formulations has less thermal and chemical stability over a broad range of conditions; increases the toxicity hazards to the applicators and thereby decreasing the safety of applicators at the time of handling and spraying the pesticides. Further some OD formulation with less suitable formulation excipients may lead to have less leaf penetration of spray droplets and increases evaporation loss and minimize the absorption of active ingredients.
Therefore, there is further need and scope in the formulation development of the OD formulation comprising one or more active ingredients with better stability profile and increases the synergistic effect of the active ingredients, reduces the toxicity with less introduction of toxic material in environment, which may reduce the dose of the pesticides and eventually produce less chemicals in environment, with better safety profile for contact and systemic herbicides.
US9439435B2 relates to an herbicidal composition. The present invention relates to an herbicidal controlling weed in a crop by applying to weeds having an average height ranging from about 4 inches to about 8 inches a herbicidally effective amount of a composition that includes (a) fluthiacet-methyl and (b) a p-hydroxyphenylpyruvate dioxygenase (HPPD) inhibitor. The present invention relates to a formulation of herbicidal composition and a method for controlling undesired vegetation.
WO2021240489A2 relates to a synergistic herbicidal composition comprising imidazolinone herbicide, a sulfonylurea herbicide and an aryloxyphenoxy propionate herbicide. Particularly, the present invention relates to the herbicidal composition of (A) Imazethapyr or a salt or adduct thereof and (B) Chlorimuron ethyl or a salt or adduct thereof and (C) Clodinafop propargyl or a salt or adduct thereof. More particularly, the present invention relates to a formulation of herbicidal composition and a method for controlling undesired vegetation.
US20180084778A1 relates to a Synergistic herbicidal composition comprising (A) a compound of formula (I) wherein R1 is methyl, methoxy or chloro, R2 is methyl or chloro and A is a substituted heteroaryl group, or an N-oxide or salt form thereof, and (B) one or more further herbicides; as well as the use of such compositions in controlling plants or inhibiting plant growth.
Therefore there is further need to formulate the novel OD formulation which increases the synergistic activities between active ingredients by using the appropriate formulation excipients; enhance the weed control efficiency; reduce the doses of active ingredients and thereby minimizing the pesticidal load into the environment; has thermal and chemical stability over a broad range of conditions; reduces the toxicity hazards to the applicators, i.e. improves the safety of applicators at the time of handling and spraying the pesticides; and improves leaf penetration of spray droplets, retard evaporation loss and enhance the absorption of active ingredients.
There is however a need for improvement of OD formulations. Many times, it has been found that single or combination of active ingredients requires a high loading dose for the better results. Further this will create a higher loading of the pesticides in the environment. Further many of the OD formulation recipe is prone to lose stability when exposed to the higher temperature. In addition, there are higher chances of formulation applied gets evaporated resulting in the loss of the active ingredients before penetration.
Therefore, one object of the present invention is to provide improved combinations (A) Fluthiacet methyl (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazone or their salt (C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt. Another object of the present invention is to provide a method and a composition for controlling harmful weeds.
Further object of the present invention is to provide suitable formulation excipients for the present Oil Dispersion formulation in order to produce stable and synergistic formulation.
Another object of the present invention is to provide a method and a composition for the OD formulation.
Embodiment of the present invention can ameliorate one or more of the above-mentioned problems.
Inventors of the present invention have surprisingly found that the novel synergistic mixture of OD formulation for plant treatment comprising of (A) Fluthiacet methyl (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazone or their salt(C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt can provide solution to the above mentioned problems.
SUMMARY OF INVENTION:
Therefore an aspect of the present invention provides a synergistic agrochemical Oil Dispersion (OD) composition comprising bioactive amount (A) Fluthiacet methyl (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazone or their salt(C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt thereof; along with formulation excipients.
Further aspect of the present invention is to provide novel agrochemical Oil Dispersion (OD) formulation comprising at least one active ingredient suspended in oil phase shows synergistic activity and stability over wide range of the conditions.
Yet another object of the present synergistic agrochemical Oil Dispersion (OD) composition comprising bioactive amount of (A) Fluthiacet methyl is in the range of 0.5% to 5% w/w (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazone or their salt in the range of 0.5% to 40% w/w (C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt in the range of1% to 40% w/w thereof that controls harmful weeds.
Further aspect of the present synergistic Oil Dispersion (OD) composition is to provide selection of suitable formulation excipients selected from category of super wetting-spreading-penetrating agent, carrier or solvent, emulsifying agent, dispersing agent, stabilizers, antifoaming agent, preservative, anti-freezing agent and buffering agents.
Another aspect of the present invention is to provide synergistic agrochemical Oil Dispersion (OD) formulation comprising Super Wetting-spreading-penetrating agent- Polyalkyleneoxide modified Heptamethyl trisiloxane (Modified trisiloxane).
In a further embodiment of the present invention, an herbicide safeners can be used in the present composition and is selected from benoxacor, cloquintocet, cloquintocet mexyl, cyprosulfamide, cyometrinil, dicyclonon, dichlormid, dietholate, fenclorim, fenchlorazole, fenchlorazole ethyl, furilazole, fluxofenim, flurazole, isoxadifen, isoxadifen ethyl, mefenpyr, mefenpyr diethyl, mephenate, naphthalic anhydride, oxabetrinil.
Further aspect of the present invention is to provide synergistic agrochemical Oil Dispersion (OD) formulation comprising carrier or solvent selected from pongamia/karanja/karanj (Millettia pinnata/Pongamia pinnata/Pongamia glabra) oil alone or palm (Elaeis spp.) oil (Palm oil and palm kernel oil) alone or mahua (Madhuca longifolia) oil or blend of pongamia oil and palm oil or blend of pongamia oil and mahua oil or blend of pongamia oil and jojoba (Simmondsia chinensis) or blend of palm oil and jojoba oil or blend of pongamia oil and vegetable oil or blend of palm oil and mahua oil or blend of palm oil and jojoba oil or blend of palm oil and vegetable oil or blend of pongamia oil, palm oil and mahua oil or blend of pongamia oil, palm oil and jojoba oil, blend of pongamia oil, palm oil and vegetable oil.
In a further embodiment of the present invention, herbicide selected from different group of herbicides. The present synergistic agrochemical Oil Dispersion (OD) composition comprising bioactive amount (A) Fluthiacet methyl (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazone or their salt (C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt thereof described herein is obtained by a process comprising a step of
a) Preparing the liquid premix by charging the oil or solvent or both followed by adding super wetting-spreading-penetrating agent.
b) The further step is adding the active ingredients into the premixed through milling for the proper size distribution.
c) Further adding the thickening agent followed by stirring the slurry get prepared by milling process to prepare the final formulation.
These agrochemical oil dispersion formulations prepared above can be used in spray mixtures in agriculture.
DETAILED DESCRIPTION OF THE INVENTION:
Formulation technology in the field of agriculture is now seen as an “enabling technology” which can provide safe and effective products which are convenient to use. It can also modify the toxicity of active ingredients and improve their ability to target a specific pest. At a time when the discovery of new agrochemical compounds is more difficult and certainly a high risk and expensive operation, formulation technology can extend the useful patent life of an active ingredient. It can also provide a competitive edge by improving the product quality of existing formulations, or by introducing a new formulation of an active ingredient.
OD formulations are non-aqueous dispersion intended for dilution into water before use and represent the most complex of the non-aqueous suspension formulations. Oil dispersion (OD) formulations consist of a suspension of a solid technical in oil. The oil also serves as a carrier or solvent for additives. The oil dispersion is usually dispersed in water prior to spraying.
An Oil Dispersion is a non-aqueous suspension concentrate. It combines a very good biological efficacy with an environmentally friendly formulation. The active ingredient is dispersed in oils or methylated crop oils.
Oil Dispersion formulation comprises with some features as it comprises no aromatic solvent or reduced amount of aromatic solvent; is non-aqueous formulation; non-flammable and low volatility; higher efficiency.
Oil Dispersion (OD) has several advantages over standard formulations. Emulsifiable Concentrate (ECs) formulations are under a strong regulatory pressure to replace toxic and flammable solvents with a less toxic and non-flammable solutions. The novel ODs meet these needs: the oil content gives a favourable eco-toxicological profile guarantying a very high biological efficacy. Further the novel OD formulations are non-toxic and non-flammable formulations. Over the EC formulation the novel OD formulation is having very high biological efficacy.
Suspension concentrate (SC) formulations are very safe formulations, but the aqueous media is normally not ideal to boost the pesticide’s biological efficacy. As an agriculture growers’ standard practice, tank mix adjuvants are added to guarantee a higher performance. The novel OD, with its oil content, guarantees the best biological results. For water sensitive active ingredients, the novel OD represents the sole technical solution to liquid formulation. The novel OD formulation over SC formulation is very safe formulation along with high biological performance. Further the novel OD formulation is ideal for all the active ingredients not stable in water.
Water dispersible granules (WDG) formulations are very safe but quite expensive. Optimal biological efficacy requires adjuvants. The novel OD, with its oil content and better particle size distribution, combines high efficacy with better cost. The novel OD formulation over WDG has economic significance as having better efficacy at a lower cost.
OD formulation presents several challenges in preparation and manufacturing phase. To obtain a good and stable formulation over time, optimal formulation additives are required in addition to optimum processes. Particular attention must be given to the choice of all the formulation excipients. Its dispersion and activation are key to the stability of the formulation over time.
Some important requirements of the formulation excipients are perfectly dispersible in oil, no phase separation, easy milling, with no agglomeration, excellent oil emulsification, stable dilution, good coverage and penetration, even distribution through the whole formulation, provide the right yield value of active ingredients.
Therefore an aspect of the present invention provides a synergistic agrochemical Oil Dispersion (OD) composition comprising bioactive amount (A) Fluthiacet methyl (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazone or their salt (C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt thereof.
Further aspect of the present invention is to provide novel agrochemical Oil Dispersion (OD) formulation comprising at least one active ingredient suspended in oil phase shows synergistic activity and stability over wide range of the conditions.
In another preferred embodiment of the invention, synergistic Weed controlled according to the method of the invention.
The term "synergistic", as used herein, refers the combined action of two or more active
agents blended together and administered conjointly that is greater than the sum of their individual effects.
In an embodiment present inventors combination of the present invention synergistic agrochemical Oil Dispersion (OD) composition comprising bioactive amount of (A) Fluthiacet methyl (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazone or their salt(C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt.
In an embodiment present invention, an herbicide safeners are selected from Benoxacor, cloquintocet, cloquintocet mexyl, cyprosulfamide, cyometrinil, dicyclonon, dichlormid, dietholate, fenclorim, fenchlorazole, fenchlorazole ethyl, furilazole, fluxofenim, flurazole, isoxadifen, isoxadifen ethyl, mefenpyr, mefenpyr diethyl, mephenate, naphthalic anhydride, oxabetrinil.
In an embodiment of the present invention is to provide synergistic agrochemical Oil Dispersion (OD) formulation comprising formulation excipients from the category of Super Wetting-spreading-penetrating agent, Solvent, emulsifying agent, dispersing agent, stabilizers, antifoaming agent, preservative, anti-freezing agent and buffering agents.
In an embodiment Super Wetting-spreading-penetrating agent for the present Oil Dispersion formulation is Polyalkyleneoxide modified Heptamethyl trisiloxane (Modified trisiloxane).
In an embodiment solvent is selected form pongamia/karanja/karanj (Millettia pinnata/Pongamia pinnata/Pongamia glabra) oil alone or Palm (Elaeis spp.) oil (Palm oil and palm kernel oil) alone or Mahua (Madhuca longifolia) oil or blend of pongamia oil and palm oil or blend of pongamia oil and mahua oil or blend of pongamia oil and jojoba (Simmondsia chinensis) or blend of palm oil and jojoba oil or blend of pongamia oil and vegetable oil or blend of palm oil and mahua oil or blend of palm oil and jojoba oil or blend of palm oil and vegetable oil or blend of pongamia oil, palm oil and mahua oil or blend of pongamia oil, palm oil and jojoba oil, blend of pongamia oil, palm oil and vegetable oil. The vegetable oil may be any one or mixture of two or more selected from soybean (Glycine max) oil, groundnut (Arachis hypogaea) oil, rapeseed (Brassica napus subspecies) oil, mustard (Brassica juncea) oil, sesame (Sesamum indicum) oil, corn (Zea mays) oil, rice (Oryza sativa) bran oil, castor (Ricinum communis) seed oil, cotton (Gossypium hirsutum) seed oil, linseed (Linum usitatissimum), coconut (Cocos nucifera) oil, sunflower (Helianthus annuus) oil, safflower (Carthamus tinctorius) seed oil.
Preferably solvent for the present formulation is selected from pongamia oil, palm oil, mahua oil, jojoba oil, vegetable oil and their mixtures may be alkylated or ethoxylated or epoxylated or esterified. Examples methyl ester of pongamia oil, methyl ester of palm oil, methyl ester of pongamia oil and palm oil, methyl ester of pongamia oil and mahua oil, methyl ester of pongamia oil and jojoba oil, methyl ester of pongamia oil and vegetable oil, methyl ester of palm oil and mahua oil, methyl ester of palm oil and jojoba oil, methyl ester of palm oil and vegetable oil, methyl ester of pongamia oil+palm oil+vegetable oil etc.
In an embodiment Emulsifier used herein for present Oil Dispersion (OD) formulation is selected from castor oil ethoxylates, alcohol ethoxylates, fatty acid ethoxylates, sorbitan ester ethoxylates, sulphosuccinate, calcium salts of dodecylbenzene sulphonate, alkylammonium salts of alkylbenzene sulphonate, alkylsulphosuccinate salts, ethylene oxide-propylene oxide block copolymers, ethoxylated alkylamines, octylphenol ethoxylate, ethoxylated alkyl phenols, ethoxylated sorbitol oleates, polyoxyethylene sorbitan monolaurate etc.
In an embodiment Dispersing agent used herein for present Oil Dispersion (OD) formulation is selected from Preparation of condensed naphthalene sulfonate, Propoxylated Ethoxylated copolymer monoalkylether (ethylhexanol), alkyl sulfonates, alkyl benzene sulfonates, alkyl aryl sulfonates, alkylphenolalkoxylates, tristyrylphenol ethoxylates, natural or synthetic fatty ethoxylate alcohols, natural or synthetic fatty acid alkoxylates, natural or synthetic fatty alcohols alkoxylates, alkoxylated alcohols (such as n-butyl alcohol poly glycol ether), block copolymers (such as ethylene oxide-propylene oxide block copolymers and ethylene oxide-butylene oxide block copolymers), fatty acid-polyalkylene glycol condensates, polyamine-fatty acid condensates, polyester condensates, salts of polyolefin condensates, sodium ligno sulfonate, sodium polycarboxylate, EO/PO based copolymer, phenol sulfonate, sodium methyl oleoyl taurate, styrene acrylic acid copolymer, propyleneoxide-ethyleneoxide-copolymer, polyethylene glycol 2,4,6-tristyrylphenyl ether, tristyrylphenol-polyglycolether-phosphate, tristyrylphenole with 16 moles EO, tristyrylphenol-polyglycolether-phosphate, oleyl-polyglycolether with ethylene oxide, tallow fattyamine polyethylene oxide, nonylphenol polyglycolether with 9-10 moles ethylene oxide.
In an embodiment Stabilizers used herein for present Oil Dispersion (OD) formulation is selected from hectorite clay, aluminium magnesium silicate, bentonite clay, silica, attapulgite clay.
In an embodiment Antifoaming agent used herein for present Oil Dispersion (OD) formulation is selected from silicone oil, silicone compound, C10~C20 saturated fat acid compounds or C8~C10 aliphatic alcohols compound, silicone antifoam emulsion, dimethylsiloxane, polydimethyl siloxane etc.
In an embodiment Anti-freezing agent used herein for present Oil Dispersion (OD) formulation is selected from ethylene glycol, propane diols, glycerine or the urea, glycol (Monoethylene glycol, Diethylene glycol, Polypropylene glycol, Polyethylene glycol), glycerine, urea, magnesium sulfate heptahydrate, sodium chloride etc.
In an embodiment Preservativeused herein for present Oil Dispersion (OD) formulation is selected from1, 2-benzisothiazolin-3(2H)-one, sodium salt, sodium benzoate, 2-bromo-2-nitropropane-1, 3-diol, formaldehyde, sodium o-phenylphenate, 5-chloro-2-methyl-4-isothiazolin-3-one & 2-methyl-4-isothiazolin-3-one, Butyl hydroxyl toluene.
In an embodiment Buffering agentused herein for present Oil Dispersion (OD) formulation is selected from Citric acid, sodium carbonate, sodium bicarbonate, sulphuric acid, hydrochloric acid, sodium hydroxide, potassium hydroxide, acetic acid, sorbic acid.
In an embodiment Polar Cosolvent (optionally) used herein for present Oil Dispersion (OD) formulation is selected from cyclohexanone, acetophenone, butanol, n-octanol, n-propanol, 1-hexanol, propylene carbonate, n-methyl-2-pyrrolidone.
The synergistic agrochemical Oil Dispersion (OD) composition comprising bioactive amount of (A) Fluthiacet methyl (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazone or their salt(C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt thereof. The present invention used to control all kind of monocots, dicots and sedges weeds. The present invention also controls annual and perennial weeds. The most common weeds controlled by present inventions are Abutilon indicum, Acalypha indica, Acanthocereus hispidum, Achyranthes aspera, Aerva tomentosa, Ageratum conyzoides, Alhagi camelorum, Amaranthus hybridus, Amaranthus spinosus, Amaranthus viridis, Ammannia baccifera, Anagallis arvensis, Argemone mexicana, Artemisia nilagiricia, Asphodelus tenuifolius, Avena fatua, Avena ludoviciana, Bidens pilosa, Boerhaavia diffusa, Boerhavia repanda, Brachiaria mutica, Brassica kaber, Bromus tectorum, Calotropis gigantea, Cannabis sativa, Carthamus axyacantha, Cassia tora, Celosia argentea, Centella asiatica, Chenopodium album, Chenopodium murale, Chloris barbata, Chrozophora rottlerii, Cichorium intybus, Cirsium arvense, Clitoria ternatea, Cnicus arvensis, Commelina benghalensis, Commelina communis, Convolvulus arvensis, Conyza canadensis, Corchorus acutangulus, Coronopus didymus, Crotalaria serice, Cucumis callosus, Cuscuta campestris, Cuscuta chinensis, Cynodon dactylon, Cyanotis axillaris, Cyperus esculenthus, Cyperus iria, Cyperus rotundus, Dactyloctenium aegyptium, Datura stramonium, Daucus carota, Digera arvensis, Digitaria sanguinalis, Dinebra retroflexa, Echinochola colonum, Echinochola crusgalli, Eclipta alba, Eichhornia crassipes, Elephantopus scaber, Eleusine indica, Eragrostis major, Euphorbia geniculata, Euphorbia hirta, Fimbristylis miliacea, Fumaria indica, Gynandropsis gynandra, Heliotropium indicum, Indigofera glandulosa, Ipomea aquatica, Lantana camara, Lathyrus aphaca, Launaea asplenifolia, Launaea nudicaulis, Leucas aspera, Ludwigia parviflora, Marsilea quadrifoliata, Medicago denticulate, Mimosa pudica, Melilotus alba, Melilotus indica, Ocimum canum, Oenothera biennis, Opuntia dillenil, Orobanche ramosa, Oryza longistaminata, Oryza sativa, Oxalis corniculata, Oxalis latifolia, Parthenium hysterophorus, Paspalum sanguinale, Phalaris minor, Phyllanthus niruri, Physalis minima, Polypogon monspeliensis, Portulaca oleracea, Prosopis juliflora, Rumex dentatus, Saccharum spontaneum, Scirpus spp., Stearia glauca, Seteria viridis, Sida spinosa, Silene antirrhina, Sisymbrium irio, Solanum nigrum, Solanum surattense, Sonchus oleraceous, Sorghum halepense, Spergula arvensis, Sphenocleazeylanica Gaertn, Striga asiatica, Tagetes minuta, Trianthema monogyna, Trianthema portulacastrum, Tribulus terrestris, Trigonelia polycerata, Vernonia cinerea, Vicia sativa and Xanthium strumarium.
The present inventors believe that the combination of the present invention synergistic agrochemical Oil Dispersion (OD) composition comprising bioactive amount of (A) Fluthiacet methyl (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazoneor their salt(C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt.
Non aqueous formulation of Fluthiacet methyl and herbicide(s) may be used to control unwanted vegetation on crop and non-crop lands Examples of the crops on which the present compositions may be applied include GMO (Genetically Modified Organism) and Non GMO traits, hybrids and conventional varieties of Soybean (Glycine max), Groundnut/Peanut (Arachis hypogaea), Green gram (Vigna radiata), Black gram (Vigna mungo), Chickpea (Cicer aritinum), Cowpea (Vigna unguiculata), Red gram (Cajanus cajan), French bean (Phaseolus vulgaris), Indian bean (Lablab purpureus), Horse gram (Macrotyloma uniflorum), Field pea (Pisum sativum), Cluster bean (Cyamopsis tetragonoloba), Lentils (Lens culinaris).
Crops are to be understood as also including those crops which have been rendered tolerant to herbicides or classes of herbicides (e.g. ALS-, GS-, EPSPS-, PPO-, ACCase- and HPPD-inhibitors) by conventional methods of breeding or by genetic engineering. An example of a crop that has been rendered tolerant to imidazolinones, e.g. imazamox, by conventional methods of breeding is Clearfield® summer rape (canola). Examples of crops that have been rendered tolerant to herbicides by genetic engineering methods include e.g. glyphosate- and glufosinate-resistant maize varieties commercially available under the trade names RoundupReady® and LibertyLink®.
Crops are also to be understood as being those which have been rendered resistant to harmful insects by genetic engineering methods, for example Bt maize (resistant to European corn borer), Bt cotton (resistant to cotton boll weevil) and also Bt potatoes (resistant to Colorado beetle). Examples of Bt maize are the Bt 176 maize hybrids of NK® (Syngenta Seeds). The Bt toxin is a protein that is formed naturally by Bacillus thuringiensis soil bacteria. Examples of toxins, or transgenic plants able to synthesise such toxins, are described in EP-A-451 878, EP-A-374 753, WO 93/07278, WO 95/34656, WO 03/052073 and EP-A-427 529. Examples of transgenic plants comprising one or more genes that code for an insecticidal resistance and express one or more toxins are KnockOut® (maize), Yield Gard® (maize), NuCOTIN33B® (cotton), Bollgard® (cotton), NewLeaf® (potatoes), NatureGard® and Protexcta®. Plant crops or seed material thereof can be both resistant to herbicides and, at the same time, resistant to insect feeding (“stacked” transgenic events). For example, seed can have the ability to express an insecticidal Cry3 protein while at the same time being tolerant to glyphosate.
Crops are also to be understood to include those which are obtained by conventional methods of breeding or genetic engineering and contain so-called output traits (e.g. improved storage stability, higher nutritional value and improved flavour).
Other useful plants include turf grass for example in golf-courses, lawns, parks and roadsides, or grown commercially for sod, and ornamental plants such as flowers or bushes.
The present OD (Oil Dispersion) formulation comprising bioactive amount of (A) Fluthiacet methyl (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazone or their salt(C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt. Benefits of OD formulation containing fluthiacet methyl and herbicide(s):
• Non aqueous formulation improves penetration of spray droplets, retard evaporation loss and enhance the absorption of active ingredients into weed leaves.
• Increases spreading properties on leaf surfaces, better wetting of waxy leaf surfaces of some weeds so it accelerates the speed of kill and enhances the efficacy against tough to kill weeds.
• Improves rain fast properties which is very much essential during rainy season to ensure the efficacy of applied herbicide.
• Increases the synergistic activities between active ingredients.
• With the non-aqueous formulation, we can reduce the doses of active ingredients and thereby minimize the pesticidal load into the environment.
• Non aqueous formulations are without aromatic solvent, so it’s safe for the applicator and reduces the loading of aromatic solvent into the environment.
• Non aqueous formulation ensures better crop safety as it is without aromatic solvent.
• Due to High flash point (smoke points) of Pongamia (>220 °C), Palm oil (>240 °C), Jojoba oil (>290 °C), mahua oil (> 230 °C), vegetable oil (> 200 °C), the novel recipe of OD formulations is more stable and safer for storage at elevated temperature.
• Non aqueous formulations have thermal and chemical stability over a broad range of conditions.
• Non aqueous formulations have better pourability, so it will minimize the wastage.
• Non aqueous formulations are stable with a wider pH range.
• Non aqueous formulation reduces the toxicity hazards to the applicators, i.e., improves the safety of applicators at the time of handling and spraying the herbicides.
The process for preparing the present synergistic oil dispersion formulation can be modified accordingly by any person skilled in the art based on the knowledge of manufacturing the formulation. However, all such variations and modifications are covered by the scope of the present invention.
The composition of the present invention in addition to bioactive amounts of active ingredients further comprises inactive excipients including but not limited to Super Wetting-spreading-penetrating agent, carrier or solvent, dispersant or dispersing agent, emulsifying agent, anti-freezing agent, anti-foam agent, preservatives and buffering agent.
Examples of super wetting-spreading-penetrating agent used herein for present OD (Oil Dispersion) formulation include but not limited to Polyalkyleneoxide modified Heptamethyl trisiloxane (Modified trisiloxane).
Polyalkyleneoxide modified heptamethyltrisiloxane: Polyalkyleneoxide modified heptamethyltrisiloxane can improve the penetration effect of pesticides and reduce the spray volume. It is used in the fields of pesticides, herbicides, insecticides, acaricides, fungicides, plant growth regulating agents, and other aspects. (Polyalkyleneoxide modified heptamethyltrisiloxane, a registered product of GE Silicones)
Molecular formula: (C2H4O)n•C11H30O3Si3
Examples of carrier or solvents used herein for present Oil dispersion (OD) formulation include but not limited to pongamia/karanja/karanj (Millettia pinnata/Pongamia pinnata/Pongamia glabra) oil alone or palm (Elaeis spp.) oil (Palm oil and palm kernel oil) alone or mahua (Madhuca longifolia) oil alone or blend of pongamia oil and palm oil or blend of pongamia oil and mahua oil or blend of pongamia oil and jojoba (Simmondsia chinensis) or blend of palm oil and jojoba oil or blend of pongamia oil and vegetable oil or blend of palm oil and mahua oil or blend of palm oil and jojoba oil or blend of palm oil and vegetable oil or blend of pongamia oil, palm oil and mahua oil or blend of pongamia oil, palm oil and jojoba oil, blend of pongamia oil, palm oil and vegetable oil.The vegetable oil may be any one or mixture of two or more selected from soybean (Glycine max) oil, groundnut (Arachis hypogaea) oil, rapeseed (Brassica napus subspecies) oil, mustard (Brassica juncea) oil, sesame (Sesamum indicum) oil, corn (Zea mays) oil, rice (Oryza sativa) bran oil, castor (Ricinum communis) seed oil, cotton (Gossypium hirsutum) seed oil, linseed (Linum usitatissimum), coconut (Cocos nucifera) oil, sunflower (Helianthus annuus) oil, safflower (Carthamus tinctorius) seed oil.
All the solvents or combination or blend thereof, used hereby for the present OD formulation may be present in their alkylated or ethoxylated or epoxylated or esterified form. Examples include methyl ester of pongamia oil, methyl ester of palm oil, methyl ester of mahua oil, methyl ester of pongamia oil and palm oil, methyl ester of pongamia oil and mahua oil, methyl ester of pongamia oil and soybean oil etc.
All the said oils used as a carrier or diluent are procured from the vendor.
Pongamia oil is derived from the seeds of the Millettia pinnata tree, which is native to tropical and temperate Asia. Millettia pinnata, also known as Pongamia pinnata or Pongamia glabra, is common throughout Asia and thus has many different names in different languages, many of which have come to be used in English to describe the seed oil derived from M. pinnata; Pongamia is often used as the generic name for the tree and is derived from the genus the tree was originally placed in. Other names for this oil include honge oil, kanuga oil, karanja oil, and pungai oil.
Pongamia oil is extracted from the seeds by expeller pressing, cold pressing, or solvent extraction. The oil is yellowish orange to brown in colour. It has a high content of triglycerides, and its disagreeable taste and odour are due to bitter flavonoid constituents including karanjin, pongamol, tannin and karanjachromene. The physical properties of crude pongamia oil are as flash point of the pongamia oil is 225°C.
Its fruits are used in abdominal remedies. Its seeds are used in tumor treatment. Oil is used for curing rheumatism. Leaves are used against Micrococcus. Their leaves juices are used for the treatment of diarrhea cold and cough. It has curative effect for leucoderma and itches. Its oil is used as a lubricant, water paint binder. Utilization of Seed Cake as a Manure for having the proper N, P & K content and ratio. As a material for biogas (Methane) production. As a Material for Producing Proteins for Food, Pharmaceutical and Industrial Applications by Chemical and Biochemical Technologies. Production of Soluble Fibers for Food Uses.
It is medium sized tree. The oil content varies from 27- 39%. Its cake is used as pesticide and fertilizer. The deoiled cake when applied to soil, has pesticidal value, especially against nematodes and also helps in improving soil fertility. Karanja is often planted in home steads as a shade or ornamental tree and in avenue planting along roadside and canals. It is preferred species help in controlling soil erosion and binding sand dunes due to its dense network of lateral roots.
The persistence of karanj is greater than other tested botanical insecticides. The dosages at 1 and 2% of karanj oil give better control of insect pests compared with lower concentrations. Karanj oil and karanjin shows greater biological activity than other karanj extracts. The karanj oil shows good synergistic effect with a number of chemical insecticides. Therefore, karanj has great potential to be used as biopesticide because of its antifeedant; oviposition deterrent, ovicidal, roachicidal, juvenile hormone activity and insecticidal properties against a wide range of insect pests [Mukesh Kumar a & Ram Singh, Department of Entomology, Potential of Pongamia glabra Vent as an Insecticide of Plant Origin, CCS Haryana, Agricultural University, Hisar, 125 004, India, Published online: 24 Apr 2012].
Botanical pesticides are also very potent insecticides and due to their composition, they can help to fight the global problem of insects developing resistance to insecticides. Insecticides based on karanja oil shows efficiency against L. decemlineata larvae at different concentrations [ Katerina Kovarikova and Roman Pavela; United Forces of Botanical Oils: Efficacy of Neem and Karanja Oil against Colorado Potato Beetle under Laboratory Conditions; Plants 2019, 8, 608; doi:10.3390/plants8120608].
The karanja (Pongamia pinnata) seeds can be used as a potential source of oil and protein which can be used for the development of bioactive chemicals by some chemical modifications. These chemicals are biodegradable, environment friendly, and available in sufficient quantities as cheap raw material and can be effectively used for the development of eco-friendly lead molecules in pesticidal formulations for the management of fungal pathogens of agriculture as well as forests. [Neelu Singh and R. K. Verma Tropical Forest Research Institute, Jabalpur-482021, Madhya Pradesh, India]
Pongamia pinnata extract of leaves, barks, root and seeds possessed antifeedant activity and insecticides, anti-inflammatory activity, antiplasmodial properties. Simin et al., (2001)reported methanolic extracts of the seeds of Pongamia pinnata possessed antibacterial and phytotoxicity properties. Muruganandan et al., (2000) reported the extracts of Pongamia pinnata seeds were used for anti-inflammatory activity. Kurkure et al., (2001) studied Pongamia pinnata stem bark therapeutically as an antiseptic in skin diseases and for its wound healing properties. [Digamber R. More, Department of Botany, L.B.S. College, Dharmabad. Nanded. 431809 Maharashtra, India, Mirza M. Vaseem Baig; Department of Botany, Yeshwant Mahavidyalaya, Nanded. 431602 Maharashtra, India]
Palm oil is an edible vegetable oil derived from the mesocarp (reddish pulp) of the fruit of the oil palms, primarily the African oil palm Elaeis guineensis, and to a lesser extent from the American oil palm Elaeis oleifera and the maripa palm Attalea maripa.
The use of palm oil in food and beauty products has attracted the concern of environmental groups; the high oil yield of the trees has encouraged wider cultivation, leading to the clearing of forests in parts of Indonesia and Malaysia to make space for oil-palm monoculture. This has resulted in significant acreage losses of the natural habitat of the three surviving species of orangutan. One species in particular, the Sumatran orangutan, has been listed as critically endangered.
PME (Palm-based Methyl Esters) as carrier solvents appear to enhance pesticide efficacy, which may allow for a reduction in dosage or frequency of application, help to control adverse effects and reduce the cost spent on pesticides. Therefore, PME as a carrier solvent in pesticide formulations is a promising prospect for the agrochemical industry [ Sumaiyah Megat Nabil Mohsin; Ismail Ab Raman; Zafarizal Aldrin Azizul Hasan and Zainab Idris; Palm-based Methyl Esters as Carrier Solvents in Pesticide Formulations, Technical Report, January 2018, Page no. 32-38].
Jojoba oil is the liquid produced in the seed of the Simmondsia chinensis (jojoba) plant, a shrub, which is native to southern Arizona, southern California, and north-western Mexico. The oil makes up approximately 50% of the jojoba seed by weight. The terms "jojoba oil" and "jojoba wax" are often used interchangeably because the wax visually appears to be a mobile oil, but as a wax it is composed almost entirely (~97%) of monoesters of long-chain fatty acids and alcohols (wax ester), accompanied by only a tiny fraction of triglyceride esters. This composition accounts for its extreme shelf-life stability and extraordinary resistance to high temperatures, compared with true vegetable oils.
The vegetable Oil for preparing blend with karanj oil or palm oil or jojoba oil used herein as solvent or carrier for present Oil dispersion (OD) formulation include but not limited to any one or mixture of two or more selected from soybean (Glycine max) oil, groundnut (Arachis hypogaea) oil, rapeseed (Brassica napus subspecies) oil, mustard (Brassica juncea) oil, sesame (Sesamum indicum) oil, corn (Zea mays) oil, rice (Oryza sativa) bran oil, castor (Ricinum communis) seed oil, cotton (Gossypium hirsutum) seed oil, linseed (Linum usitatissimum), coconut (Cocos nucifera) oil, sunflower (Helianthus annuus) oil, safflower (Carthamus tinctorius) seed oil.
Examples of buffering agent used herein for present Oil dispersion (OD) formulation is selected Citric acid, sodium carbonate, sodium bicarbonate, sulphuric acid, hydrochloric acid, sodium hydroxide, potassium hydroxide, acetic acid, sorbic acid.
A dispersant or a dispersing agent is a substance which adsorbs onto the surface of particles and helps to preserve the state of dispersion of the particles and prevents them from re-aggregating. Examples of dispersing agent used herein for used herein for present OD (Oil Dispersion) formulation include but not limited to preparation of condensed naphthalene sulfonate, propoxylated Ethoxylated copolymer monoalkylether (ethylhexanol), alkyl sulfonates, alkyl benzene sulfonates, alkyl aryl sulfonates, alkylphenolalkoxylates, tristyrylphenol ethoxylates, natural or synthetic fatty ethoxylate alcohols, natural or synthetic fatty acid alkoxylates, natural or synthetic fatty alcohols alkoxylates, alkoxylated alcohols (such as n-butyl alcohol poly glycol ether), block copolymers (such as ethylene oxide-propylene oxide block copolymers and ethylene oxide-butylene oxide block copolymers), fatty acid-polyalkylene glycol condensates, polyamine-fatty acid condensates, polyester condensates, salts of polyolefin condensates, sodium ligno sulfonate, sodium ploycarboxylate, EO/PO based copolymer, phenol sulfonate, sodium methyl oleoyl taurate, styrene acrylic acid copolymer, propyleneoxide-ethyleneoxide-copolymer, polyethylene glycol 2,4,6-tristyrylphenyl ether, tristyrylphenol-polyglycolether-phosphate, tristyrylphenole with 16 moles EO, tristyrylphenol-polyglycolether-phosphate, oleyl-polyglycolether with ethylene oxide, tallow fattyamine polyethylene oxide, nonylphenol polyglycolether with 9-10 moles ethylene oxide.
Antifoaming agent for the present formulation is selected from various compounds and selectively used according to the formulation. Generally, there are two types of antifoam agents, namely silicones and non-silicones. Silicones are usually aqueous emulsions of dimethyl poly siloxane while the non-silicone anti-foam agents are water- insoluble oils, such as octanol and nonanol, or silica. In both cases, the function of the anti-foam agent is to displace the surfactant from the air-water interface.
Examples of Antifoaming agent used herein for present Oil dispersion (OD) formulation include but not limited to silicone oil, silicone compound, C10~C20 saturated fat acid compounds or C8~C10 aliphatic alcohols compound, silicone antifoam emulsion, dimethyl siloxane, poly dimethyl siloxane etc.
Examples of Anti-freezing agent used herein for present Oil dispersion (OD) formulation include but not limited ethylene glycol, propane diols, glycerine or the urea, glycol (Monoethylene glycol, Diethylene glycol, Polypropylene glycol, Polyethylene glycol), glycerine, urea, magnesium sulfate heptahydrate, sodium chloride etc.
Preservative used herein for the present Oil dispersion (OD) formulation include but not limited to 1,2-benzisothiazolin-3(2H)-one, sodium salt, sodium benzoate, 2-bromo-2-nitropropane-1,3-diol, formaldehyde, sodium o-phenylphenate, 5-chloro-2-methyl-4-isothiazolin-3-one & 2-methyl-4-isothiazolin-3-one, Butyl hydroxyl toluene.
Emulsifying agent used herein for the present Oil dispersion (OD) formulation includes but not limited to castor oil ethoxylates, alcohol ethoxylates, fatty acid ethoxylates, sorbitan ester ethoxylates, sulphosuccinate, calcium salts of dodecylbenzene sulphonate,
alkylammonium salts of alkylbenzene sulphonate, alkylsulphosuccinate salts, ethylene oxide-propylene oxide block copolymers, ethoxylated alkylamines, octylphenol ethoxylate, ethoxylated alkyl phenols, ethoxylated sorbitol oleates, polyoxyethylene sorbitan monolaurate etc.
Stabilizers or stabilizing agent used herein for the present Oil dispersion (OD) formulation includes but not limited to hectorite clay, aluminium magnesium silicate, bentonite clay, silica, attapulgite clay.
Examples of Buffering agent used herein for the present Oil dispersion (OD) formulation include but not limited to Citric acid, sodium carbonate, sodium bicarbonate, sulphuric acid, hydrochloric acid, sodium hydroxide, potassium hydroxide, acetic acid, sorbic acid.
Polar Cosolvent used herein as optionally for the present Oil dispersion (OD) formulation include but not limited to cyclohexanone, acetophenone, butanol, n-octanol, n-propanol, 1-hexanol, propylene carbonate, n-methyl-2-pyrrolidone.
The present invention relates to synergistic agrochemical composition comprising of bioactive amounts of (A) Fluthiacet methyl is in the range of 0.5% to 5%w/w (B) One herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazoneor their salt in the range of 0.5% to 40%w/w (C) at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxadenor their salt in the range of 1% to 40%w/w composition.
EXAMPLE 1:
Novel OD formulation
Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% OD (Recipe: FCH-A, Novel OD)
Ingredients Percent (w/w)
Active ingredient 1 Fluthiacet methyl a.i. 1.20
Active ingredient 2 Chlorimuron ethyl a.i. 0.75
Active ingredient 3 Haloxyfop-r-methyl a.i. 12.00
Dispersing agent Tristyrylphenol-polyglycolether-phosphate 6.00
Emulsifying agent Octylphenol ethoxylate 10.00
Stabilizer Bentonite clay 1.00
Antifoaming agent Polydimethyl siloxane 0.30
Preservative 1,2-benzisothiazolin-3(2H)-one 0.30
Antifreezing agent Glycerine 6.00
Super wetting-spreading-penetrating agent Polyalkyleneoxide modified Heptamethyltrisiloxane 6.00
Carrier as solvent Methyl ester of Palm oil 56.45
Total 100.00
Active ingredients (a.i.) on the basis of 100% purity.
Storage stability- Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% OD (Recipe: FCH-A, Novel OD)
Parameters Specification (in house) Initial At 54±2 0C At 0±2 0C
Fluthiacet methyl a.i. (%) 1.14 to 1.32 1.35 1.26 1.35
Chlorimuron ethyl a.i. (%) 0.7125 to 0.825 0.80 0.76 0.80
Haloxyfop-r-methyl (%) 11.40 to 12.60 12.50 12.25 12.49
Fluthiacet methyl suspensibility (%) 80 98.50 97.90 98.60
Chlorimuron ethyl suspensibility (%) 80 98.70 98.10 98.50
Haloxyfop-r-methyl suspensibility (%) 80 97.90 97.10 98.00
pH range (1% aq. Suspension) 5.0 to 7.5 5.90 6.20 6.00
Pourability 95% min. 98.00 97.50 97.00
Specific gravity 1.00-1.10 1.05 1.05 1.05
Viscosity at spindle no. 62, 20 rpm 350-900 cps 700 710 725
Particle size (micron) D50<3, D90<10 2.5,8 2.7,8.7 2.6,8.6
Persistent foam ml (after 1 minute) max. 60 nil 2 nil
Room temperature storage
Parameters Specification (in house) 1 month 6 months 12 months
Fluthiacet methyl a.i. (%) 1.14 to 1.32 1.35 1.35 1.33
Chlorimuron ethyl a.i. (%) 0.7125 to 0.825 0.80 0.80 0.78
Haloxyfop-r-methyl (%) 11.40 to 12.60 12.50 12.50 12.49
Fluthiacet methyl suspensibility (%) 80 98.50 98.60 98.00
Chlorimuron ethyl suspensibility (%) 80 98.70 98.50 98.10
Haloxyfop-r-methyl suspensibility (%) 80 97.90 97.50 97.00
pH range (1% aq. Suspension) 5.0 to 7.5 5.90 6.20 6.00
Pourability 95% min. 98.00 97.50 97.00
Specific gravity 1.00-1.10 1.05 1.05 1.05
Viscosity at spindle no. 62, 20 rpm 350-900 cps 700 700 710
Particle size (micron) D50<3, D90<10 2.5,8 2.7,8.7 2.6,8.6
Persistent foam ml (after 1 minute) max. 60 nil 2 nil
The novel OD formulation recipe of Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% OD (Recipe: FCH-A, Novel OD) meets all in-house specifications for storage stability studies in laboratory (at 54±2 C & At 0±2 C for 14 days) and room temperature (for 12 months).
Manufacturing process for 100 kg batch of Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% OD (Recipe: FCH-A, Novel OD).
Step 1: 15% Bentonite clay Solution Preparation:
Add 10 kg of Bentonite clay in to 90 kg of Methyl ester of Palm oil and also and homogenized till it gets completely dissolved. It must be kept for 12-18 hour prior to use.
Step 2: OD Premix:
Charge 46.45 kg of Methyl ester of Palm oil into a designated vessel for OD production.
Now add 6.0 kg of Tristyrylphenol-polyglycolether-phosphate, 10.0 kg of Octylphenol ethoxylate, 6.0 kg of Glycerine, 0.3 kg of 1,2-benzisothiazolin-3(2H)-one and 0.15 kg of Polydimethyl siloxane homogenise the contents for 45 – 60 minutes using high shear homogeniser.
Add 1.20 kg of Fluthiacet methyl technical, 0.75 kg of Chlorimuron ethyl technical and 12.0 kg of Haloxyfop-r-methyl technical, into this premix and homogenized for 30-45 minutes.
Add remaining 0.15 kg of Silicon antifoam, 6.0 kg of Polyalkyleneoxide modified Heptamethyltrisiloxane and 10 kg of 10 % Bentonite solution after milling to avoid foaming.
Step 3: Send this final formulation to QC for quality check.
OD formulation without wetting agent.
Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% OD (Recipe: FCH-B, conventional OD):
Ingredients Percent (w/w)
Fluthiacet methyl a.i. 1.20
Chlorimuron ethyl a.i. 0.75
Haloxyfop-r-methyl a.i. 12.00
Tristyrylphenol-polyglycolether-phosphate 6.00
Octylphenol ethoxylate 10.00
Silica 1.50
Polydimethyl siloxane 0.30
1,2-benzisothiazolin-3(2H)-one 0.30
Polypropylene glycol 6.00
Methyl ester of Palm oil 61.95
Total 100.00
Active ingredients on the basis of 100% purity.
Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% SE (conventional)
Ingredients Percent (w/w)
Fluthiacet methyl a.i. 1.20
Chlorimuron ethyl a.i. 0.75
Haloxyfop-r-methyl a.i. 12.00
Tristyrylphenol phosphate potassium salt 3.00
Sodium salt of naphthalene sulfonate condensate 2.00
Aromatic solvent C-9 15.00
Styrene acrylic acid copolymer 3.00
Suspending agent (Aluminum Magnesium Silicate) 1.50
Antifoaming agent (Dimethyl poly siloxane) 0.20
Preservative (1,2- benzisothiazoline-3-one) 0.20
Antifreezing agent (Polypropylene glycols) 5.00
Thickner (Xanthan gum) 0.15
Water 56.00
Total 100.00
Active ingredients on the basis of 100% purity.
Fluthiacet methyl 2.4%+Chlorimuron ethyl 1.5%+Haloxyfop-r-methyl 24% WG (conventional)
Ingredients Percent (w/w)
Fluthiacet methyl a.i. 2.40
Chlorimuron ethyl a.i. 1.50
Haloxyfop-r-methyl a.i. 24.00
Sodium salt of naphthalene sulfonate condensate 5.00
Sodium Lauryl sulfate 3.00
Sodium ligno sulfonate 6.00
Silica 25.00
Polydimethyl siloxane 1.00
China Clay 32.10
Total 100.00
Active ingredients on the basis of 100% purity.
EXAMPLE 2:
Novel OD Recipe:
Fluthiacet methyl 0.75%+Fomesafen 15%+Propaquizafop 5% Novel OD
Ingredients Percent (w/w)
Recipe-A Recipe-B Recipe-C Recipe-D
Active ingredient 1 Fluthiacet methyl a.i. 0.75 0.75 0.75 0.75
Active ingredient 2 Fomesafen a.i. 15.00 15.00 15.00 15.00
Active ingredient 3 Propaquizafop a.i. 5.00 5.00 5.00 5.00
Dispersing agent Synthetic fatty ethoxylate alcohols 5.00 6.00 4.50 3.50
Emulsifying agent Sorbitan ester 10 ethoxylates 10.00 9.00 8.00 7.00
Stabilizer Bentonite clay 1.00 1.00 1.00 1.00
Antifoaming agent Polydimethyl siloxane 0.50 0.50 0.50 0.50
Preservative 1,2-benzisothiazolin-3(2H)-one 0.30 0.30 0.30 0.30
Antifreezing agent Glycerine 5.00 5.00 5.00 5.00
Super wetting-spreading-penetrating agent Polyalkyleneoxide modified Heptamethyltrisiloxane 5.00 7.50 10.00 12.50
Carrier as solvent Methyl ester of Palm oil and castor oil 52.45 49.95 49.95 49.45
Total 100.00 100.00 100.00 100.00
Active ingredients on the basis of 100% purity.
All the novel OD formulation recipe of Fluthiacet methyl 0.75%+Fomesafen 15%+Propaquizafop 5% OD meets all in-house specifications for storage stability studies in laboratory (at 54±2 C & At 0±2 C for 14 days) and room temperature (for 12 months).
Manufacturing process for 100 kg batch of Fluthiacet methyl 0.75%+Fomesafen 15%+Propaquizafop 5% OD (Recipe: B)
Step 1: 10 % Bentonite clay Solution Preparation:
Add 10 kg of Bentonite clay in to 90 kg of Methyl ester of Palm oil and castor oil and homogenized till it gets completely dissolved. It must be kept for 12-18 hour prior to use.
Step 2: OD Premix:
Charge 42.45 kg of Methyl ester of Palm oil and castor oil into a designated vessel for OD production.
Now add 6.0 kg of Synthetic fatty ethoxylate alcohols, 9.0 kg of Sorbitan ester 10 ethoxylates, 5.0 kg of Glycerine, 0.3 kg of 1,2-benzisothiazolin-3(2H)-one and 0.25 kg of Polydimethyl siloxane homogenise the contents for 45 – 60 minutes using high shear homogeniser.
Add 0.75 kg of Fluthiacet methyl technical, 15.0 kg of Fomesafen technical and 5.0 kg of Propaquizafop technical, into this premix and homogenized for 30-45 minutes
Add remaining 0.25 kg of Silicon antifoam, 7.5 kg of Polyalkyleneoxide modified Heptamethyltrisiloxane and 10 kg of 10 % Bentonite solution after milling to avoid foaming
Step 3: Send this final formulation to QC for quality check
EXAMPLE 3:
Novel OD Recipe
Fluthiacet methyl 0.9%+Acifluorfen sodium 14%+Quizalofop ethyl 4.5% OD
Ingredients Percent (w/w)
Active ingredient 1 Fluthiacet methyl a.i. 0.90
Active ingredient 2 Acifluorfen sodium a.i. 14.00
Active ingredient 3 Quizalofop ethyl a.i. 4.50
Dispersing agent Propoxylated Ethoxylated copolymer monoalkylether 3.00
Emulsifying agent Fatty acid ethoxylates 6.00
Stabilizer Bentonite clay 1.00
Antifoaming agent Polydimethyl siloxane 0.50
Preservative 1,2-benzisothiazolin-3(2H)-one 0.30
Antifreezing agent Propane diols 6.00
Super wetting-spreading-penetrating agent Polyalkyleneoxide modified Heptamethyltrisiloxane 6.00
Carrier as solvent Methyl ester of karanj oil 57.80
Total 100.00
Active ingredients on the basis of 100% purity.
Novel OD Recipe
Fluthiacet methyl 1%+Fomesafen 12%+Fluazifop-p-butyl 12% OD
Ingredients Percent (w/w)
Fluthiacet methyl a.i. 1.00
Fomesafen a.i. 12.00
Fluazifop-p-butyl a.i. 12.00
Tristyrylphenol ethoxylates, 6.00
Alkyl sulphosuccinate salts, 3.00
Hectorite clay 1.50
Polydimethyl siloxane 0.30
1,2-benzisothiazolin-3(2H)-one 0.20
Polypropylene glycol 6.00
Polyalkyleneoxide modified Heptamethyltrisiloxane 7.50
Methyl ester of Karanj oil and soybean oil 50.50
Total 100.00
Active ingredients on the basis of 100% purity.
Novel OD Recipe
Fluthiacet methyl 2%+Imazethapyr 12%+Quizalofop ethyl 10% OD
Ingredients Percent (w/w)
Fluthiacet methyl a.i. 2.00
Imazethapyr a.i. 12.00
Quizalofop ethyl a.i. 10.00
Propyleneoxide-ethyleneoxide-copolymer 3.50
Polyoxyethylene sorbitan monolaurate 6.00
Aluminium magnesium silicate 1.00
Polydimethyl siloxane 0.50
1,2-benzisothiazolin-3(2H)-one 0.30
Glycerine 6.00
Polyalkyleneoxide modified Heptamethyltrisiloxane 7.50
Methyl ester of palm oil and rapeseed oil 51.20
Total 100.00
Active ingredients on the basis of 100% purity.
EXAMPLE 4:
Preferred non aqueous compositions (Novel Oil Dispersion) containing Fluthiacet methyl
Compound A Compound B Compound C Active ingredients (%) Formulation Strength (%)
A B C
Fluthiacet methyl Acifluorfen sodium Clodinafop propargyl 0.9 14 8 22.90
Fluthiacet methyl Acifluorfen sodium Haloxyfop-r-methyl 0.72 11.2 9.6 21.52
Fluthiacet methyl Acifluorfen sodium Propaquizafop 0.9 14 5 19.90
Fluthiacet methyl Acifluorfen sodium Quizalofop ethyl 0.9 14 4.5 19.40
Fluthiacet methyl Acifluorfen sodium Fenoxaprop-p-ethyl 0.9 14 10 24.90
Fluthiacet methyl Fomesafen sodium Clodinafop propargyl 0.75 15 8 23.75
Fluthiacet methyl Fomesafen sodium Haloxyfop-r-methyl 0.75 15 12 27.75
Fluthiacet methyl Fomesafen sodium Propaquizafop 0.75 15 5 20.75
Fluthiacet methyl Fomesafen sodium Quizalofop ethyl 0.5 10 3 13.50
Fluthiacet methyl Fomesafen sodium Fenoxaprop-p-ethyl 0.75 15 10 25.75
Fluthiacet methyl Imazethapyr Clodinafop propargyl 1 6 8 15.00
Fluthiacet methyl Imazethapyr Haloxyfop-r-methyl 1 6 12 19.00
Fluthiacet methyl Imazethapyr Propaquizafop 2 12 10 24.00
Fluthiacet methyl Imazethapyr Quizalofop ethyl 2 12 10 24.00
Fluthiacet methyl Imazethapyr Fenoxaprop-p-ethyl 1 6 10 17.00
Fluthiacet methyl Imazamox Clodinafop propargyl 1 6 8 15.00
Fluthiacet methyl Imazamox Haloxyfop-r-methyl 1 6 12 19.00
Fluthiacet methyl Imazamox Propaquizafop 2 12 10 24.00
Fluthiacet methyl Imazamox Quizalofop ethyl 2 12 9 23.00
Fluthiacet methyl Imazamox Fenoxaprop-p-ethyl 1 6 10 17.00
Fluthiacet methyl Chlorimuron ethyl Fluazifop-p-butyl 1.2 0.75 12.5 14.45
Fluthiacet methyl Chlorimuron ethyl Haloxyfop-r-methyl 1.2 0.75 12 13.95
Fluthiacet methyl Chlorimuron ethyl Propaquizafop 2.4 1.5 10 13.90
Fluthiacet methyl Chlorimuron ethyl Quizalofop ethyl 4.8 3 18 25.80
Fluthiacet methyl Chlorimuron ethyl Fenoxaprop-p-ethyl 1.2 0.75 10 11.95
Fluthiacet methyl Fomesafen sodium Fluazifop-p-butyl 1 12 12 25.00
Fluthiacet methyl Fomesafen sodium Clethodim 1 12 12 25.00
Fluthiacet methyl Fomesafen sodium Propaquizafop 1 12 5 18.00
Fluthiacet methyl Fomesafen sodium Haloxyfop-r-methyl 1 12 12 25.00
Fluthiacet methyl Fomesafen sodium Pinoxaden 1.2 12 6 19.20
Fluthiacet methyl Acifluorfen sodium Pinoxaden 1.2 12 6 19.20
Fluthiacet methyl Chlorimuron ethyl Pinoxaden 2.4 1.5 12 15.90
Fluthiacet methyl Imazethapyr Pinoxaden 1.2 5 6 12.20
BIOLOGICAL EXAMPLES:
The synergistic pesticide action of the inventive mixtures can be demonstrated by the experiments below. A synergistic effect exists wherever the action of a combination (ready-mix) or tank mix of active ingredient is greater than the sum of the action of each of the components alone. Therefore, a synergistically effective amount or an effective amount of a synergistic composition or combination is an amount that exhibits greater pesticide activity than the sum of the pesticide activities of the individual components.
In the field of agriculture, it is often understood that the term “synergy” is as defined by Colby S.R. in an article entitled “Calculation of the synergistic and antagonistic responses of herbicide combinations” published in the journal Weeds, 1967, 15, p.20-22, incorporated herein by reference in its entirety. The action expected for a given combination of two or three active components can be calculated as follows:
The objective of the present studies was to study the benefits of non-aqueous (novel Oil Dispersion) composition of Fluthiacet methyl, one selected herbicide and at least one more herbicide.
EXPERIMENT-1
Example 1: Bio efficacy comparison of Novel OD (Oil dispersion) composition vs conventional formulations against mixed weed flora in Soybean crop.
Crop : Soybean (Glycine max)
Target weeds : mixed weed flora (Grasses, broad leaf, sedges)
Location : Indore, Madhya Pradesh
Number of Treatments: 9
Plot size : 6 m x 5 m=30 sq.m.
Application time :16 DAS (days after sowing), 2 to 4 leaf stage of weeds.
Application method : foliar spray with backpack sprayer attached flat fan nozzle.
Water volume : 400 litre per hectare
Observation Methods: Weed control (%): Species wise weed count recorded at 15and 30 DAA (Days after Application) by using 0.25 m2 (50 cm x 50 cm) quadrant, treatment wise in minimum 5 places randomly selected in the plot. The species wise weed count further grouped into Grasses and Broad Leaf weeds (BLW) and sedges. The data presented here as total weed control (grasses+broadleaf+sedges). The average of each variable was used together with the sum of all the variables per plot to calculate the percentage of control.
Phytotoxicity: The observations on crop safety i.e., phytotoxicity or adverse effect of treatments were recorded at regular intervals. All the visual phytotoxicity symptoms like plant yellowing, leaf scorching, tip burning, bleaching, necrosis, stunting, crinkling, epinasty, hyponasty. Three leaves from each selected plant were scored using 0-10 rating scale, whereas 0=No injury/phytotoxicity, 1=1 to 10%phytotoxicity, 2=11 to 20%, 3=21 to 30%.......10=91 to 100% phytotoxicity. Percent phytotoxicity was determined using the following formula.
Table 1: Bio efficacy comparison Novel OD composition vs conventional formulations.
Treatment compositions Application Rate (gai/h) Weed control (%)
15 DAA 30 DAA
T1-Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% OD (Recipe: FCH-A, Novel OD) 12+7.5+120 100.0 99.2
T2-Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% OD (Recipe: FCH-B, conventional OD) 12+7.5+120 92.6 80.4
T3-Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% SE (conventional) 12+7.5+120 91.2 78.8
T4-Fluthiacet methyl 2.4%+Chlorimuron ethyl 1.5%+Haloxyfop-r-methyl 24% WG (conventional) 12+7.5+120 89.6 77.4
T5-Fluthiacet methyl 10.3% EC+Chlorimuron ethyl 25% WP+Haloxyfop-r-methyl 10.5% EC (tank mix) 12+7.5+120 85.4 73.8
T6-Fluthiacet methyl 10.3% EC (Market product) 12 43.6 40.2
T7-Chlorimuron ethyl 25% WP+0.2% Non ionic surfactant 7.5 44.2 42.4
T8-Haloxyfop-r-methyl 10.5% EC (Market product) 120 48.8 45.6
T9-Untreated Check (UTC)- only water spray 0 0.0 0.0
Weed flora composition of trial plot: grassy weeds 50% (Echinochloa colona, Eragrostis major, Brachiaria mutica), Broad leaf weeds 50% (Commelina benghalensis, Phyllanthus niruri, Datura stramonium).
The result of field trial presented in Table 1. The results shows Novel OD composition of Fluthiacet methyl+ chlorimuron ethyl+ haloxyfop-r-methyl (T1: Recipe FCH-A) provides superior control of mixed weed flora in comparison to their conventional OD formulation (T2), conventional SE formulation (T3), conventional WG formulation (T3) and their tank mix (T4). The speed of kill of weeds was observed faster in novel OD composition (T1: Recipe FCH-A) as compared to conventional OD, SE, WG formulations and their tank mix (T4).
Table 2: Phytotoxicity symptoms.
Sr.no. Leaf scorching (%) Yellowing (%)
15 DAA 30 DAA 15 DAA 30 DAA
T1 5.73 0 4.28 0
T2 6.23 0 5.92 0
T3 8.13 0 6.28 0
T4 8.93 0 8.39 0
T5 13.58 5.82 11.28 4.28
T6 6.28 0 6.23 0
T7 2.16 0 5.75 0
T8 0 0 0 0
T9 0 0 0 0
Little scorching and yellowing were observed in T1, which was completely recovered without affecting normal plant growth at 30 DAA, whereas both leaf scorching and yellowing were severe in tank mix (T5).
EXPERIMENT-2
Example 2: Bio efficacy evaluation of Novel OD (Oil dispersion) compositions comprising of Fluthiacet methyl+Acifluorfen sodium+one more herbicide.
Crop : Soybean (Glycine max)
Target weeds : mixed weed flora (Grasses+broadleaf+sedges)
Location : Amravati, Maharashtra
Number of Treatments: 15
Plot size : 8 m x 4 m=32 sq.m.
Application time : 22 DAS (days after sowing), 2 to 6 leaf stage of weeds.
Application method : foliar spray with backpack sprayer attached flat fan nozzle.
Water volume : 440 litre per hectare
Observation Methods : Weed control (%) and phytotoxicity, same as per example 1.
Pod counts: Count the number of pods per plant, record the observations from 20 plants per plot at the time of harvest.
Table 3: Treatment details.
Sr.no. Treatment compositions Application Rate (gai/h)
T1 Fluthiacet methyl 0.9%+Acifluorfen sodium 14%+Clodinafop propargyl 8% OD 9+140+80
T2 Fluthiacet methyl 0.72%+Acifluorfen sodium 11.2%+Haloxyfop-r-methyl 9.6% OD 9+140+120
T3 Fluthiacet methyl 0.9%+Acifluorfen sodium 14%+Propaquizafop 5% OD 9+140+50
T4 Fluthiacet methyl 0.9%+Acifluorfen sodium 14%+Quizalofop ethyl 4.5% OD (Recipe: FAQ) 9+140+45
T5 Fluthiacet methyl 0.9%+Acifluorfen sodium 14%+Fenoxaprop-p-ethyl 10% OD 9+140+100
T6 Fluthiacet methyl 10.3% EC 9
T7 Sodium salt of Acifluorfen 20.1% SL 140
T8 Clodinafop propargyl 15% WP 80
T9 Haloxyfop-r-methyl 10.5% EC 120
T10 Propaquizafop 10% EC 50
T11 Quizalofop ethyl 10% EC 45
T12 Fenoxaprop-p-ethyl 9.3% EC 100
T13 Acifluorfen sodium 16.5%+Clodinafop propargyl 8% EC 165+80
T14 Fluthiacet-methyl 2.5 %+Quizalofop ethyl 10 % EC 12.5+50
T15 Untreated Check (UTC) 0
T1 to T5 are novel OD compositions, T6 to T13 are market products.
Weed flora composition of trial plot: grassy weeds 50% (Echinochloa colona, Digitaria spp., Paspalum spp.), Broad leaf weeds 45% (Commelina benghalensis, Amaranthus viridis, Digera arvensis), Sedges 5% (Cyperus rotundus).
Table 4: Bio efficacy performance of novel OD compositions in soybean crop.
Sr.no. Weed control (%) at 15 DAA Number of pods per plant Increase (%) in pods per plant over T15
observed Expected Colby ratio Synergism (Y/N)
T1 96.6 86.3 1.12 Y 65.7 54.59
T2 100.0 86.4 1.16 Y 67.3 58.35
T3 100.0 86.3 1.16 Y 67.1 57.88
T4 99.2 86.3 1.15 Y 66.4 56.24
T5 97.8 85.9 1.14 Y 65.9 55.06
T6 44.8 54.7 28.71
T7 51.4 55.8 31.29
T8 48.8 56.2 32.24
T9 49.2 55.8 31.29
T10 48.8 56.1 32.00
T11 49.0 55.4 30.35
T12 47.6 54.7 28.71
T13 90.6 63.3 48.94
T14 91.2 62.1 46.12
T15 0.0 42.5 0.00
All the novel OD compositions (T1 to T5) provides excellent weed control (>96.6%) as compared to conventional treatments (T6 to T14) and bears higher number of pods per plant, which are directly contributing to the yield.
Table 5: Phytotoxicity study.
Sr.no. Leaf scorching (%)
3 DAA 15 DAA 30 DAA
T1 10.83 2.84 0.00
T2 9.75 2.18 0.00
T3 10.27 2.58 0.00
T4 10.15 2.16 0.00
T5 10.87 2.95 0.00
T6 3.29 0.00 0.00
T7 18.84 15.38 5.23
T8 0.00 0.00 0.00
T9 0.00 0.00 0.00
T10 0.00 0.00 0.00
T11 0.00 0.00 0.00
T12 0.00 0.00 0.00
T13 22.74 16.38 5.82
T14 5.38 0.00 0.00
T15 0.00 0.00 0.00
Leaf scorching were observed in all the novel OD compositions which were recovered completely without affecting normal plant growth and does not have any negative impact on pod bearing capacity of plants.
EXPERIMENT-3
Example 3: Bio efficacy comparison of Novel OD compositions comprising of Fluthiacet methyl+Chlorimuron ethyl +one more herbicide.
Crop : Soybean (Glycine max)
Target weeds : mixed weed flora (Grasses+broadleaf+sedges)
Location : Kota, Rajasthan
Number of Treatments: 14
Plot size : 10 m x 5 m=50 sq.m.
Application time : 26 DAS (days after sowing), 4 to 8 leaf stage.
Application method : foliar spray with backpack sprayer attached flat fan nozzle.
Water volume : 500 litre per hectare
Observation Methods : Weed control (%) and phytotoxicity, same as per example 1.
Pod counts: Count the number of pods per plant, record the observations from 20 plants per plot at the time of harvest.
Table 6: Treatment details.
Sr.no. Treatment compositions Application Rate (gai/h)
T1 Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Fluazifop-p-butyl 12.5% OD 12+7.5+125
T2 Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% OD (Recipe: FCH-A, Novel OD) 12+7.5+120
T3 Fluthiacet methyl 2.4%+Chlorimuron ethyl 1.5%+Propaquizafop 10% OD 12+7.5+50
T4 Fluthiacet methyl 4.8%+Chlorimuron ethyl 3%+Quizalofop ethyl 18% OD 12+7.5+45
T5 Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Fenoxaprop-p-ethyl 10% OD 12+7.5+100
T6 Fluthiacet methyl 10.3% EC 12
T7 Chlorimuron ethyl 25% WP+ Non-Ionic surfactant 0.2% 7.5
T8 Fluazifop-p-butyl 13.4% EC 125
T9 Haloxyfop-r-methyl 10.5% EC 120
T10 Propaquizafop 10% EC 50
T11 Quizalofop ethyl 10% EC 45
T12 Fenoxaprop-p-ethyl 9.3% EC 100
T13 Quizalofop ethyl 10% EC+Chlorimuron ethyl 25% WP+Non ionicSurfactant 0.2% (tank mix) 37.5+9
T14 Untreated Check (UTC) 0
T1 toT5 are novel OD compositions, T6 to T13 are market products. Weed flora composition of trial plot: grassy weeds 60% (Echinochloa colona, Eleusine indica), Broad leaf weeds 40% (Commelina communis, Physalis minima, Digera arvensis).
Table 7: Bio efficacy evaluation of novel OD compositions in soybean.
Sr.no. Weed control (%) at 15 DAA Number of pods per plant Increase (%) in pods per plant over T14
observed expected Colby ratio Synergism (Y/N)
T1 100.0 83.7 1.19 Y 60.8 85.93
T2 100.0 83.3 1.20 Y 61.7 88.69
T3 100.0 83.6 1.20 Y 61.3 87.46
T4 98.8 83.0 1.19 Y 59.2 81.04
T5 97.4 82.6 1.18 Y 58.9 80.12
T6 39.2 46.8 43.12
T7 35.4 45.5 39.14
T8 58.6 51.2 56.57
T9 57.4 52.5 60.55
T10 58.2 51.7 58.10
T11 56.6 50.8 55.35
T12 55.8 49.3 50.76
T13 86.4 50.8 55.35
T14 0.0 32.7 0.00
All the novel OD compositions (T1 to T5) provides excellent weed control (>97.4%) as compared to conventional treatments (T6 to T13) and bears higher number of pods (> 58.9 per plant), which are directly contributing to the yield. Novel OD composition (T4) provides better efficiency and bear higher pods per plant as compared to conventional SC composition (T13).
Phytotoxicity symptoms appear in terms of yellowing and discoloration of upper foliage, which were completely recovered within 15 DAA.
EXPERIMENT-4
Example 4: Bio efficacy comparison of Novel OD compositions comprising of Fluthiacet methyl+Fomesafen+one more herbicide.
Crop : Groundnut
Target weeds : mixed weed flora (Grasses+broadleaf+sedges)
Location : Junagadh, Gujarat
Number of Treatments: 14
Plot size : 8 m x 6 m=48 sq.m.
Application time : 21 DAS (days after sowing), 2 to 4 leaf stage of weeds.
Application method : foliar spray with backpack sprayer attached flat fan nozzle.
Water volume : 450 litre per hectare
Observation Methods : Weed control (%) and phytotoxicity, same as per example 1.
Pod counts: Count the number of pods per plant, record the observations from 20 plants per plot at the time of harvest.
Table 8: Treatment details
Sr.no. Treatment compositions Application Rate (gai/h)
T1 Fluthiacet methyl 0.75%+Fomesafen 15%+Clodinafop propargyl 8% OD 7.5+150+80
T2 Fluthiacet methyl 0.75%+Fomesafen 15%+Haloxyfop-r-methyl 12% OD 7.5+150+120
T3 Fluthiacet methyl 0.75%+Fomesafen 15%+Propaquizafop 5% OD (Recipe: B) 7.5+150+50
T4 Fluthiacet methyl 0.5%+Fomesafen 10%+Quizalofop ethyl 3% OD 7.5+150+45
T5 Fluthiacet methyl 0.75%+Fomesafen 15%+Fenoxaprop-p-ethyl 10% OD 7.5+150+100
T6 Fluthiacet methyl 10.3% EC 7.5
T7 Sodium salt of Fomesafen 22.1% SL 150
T8 Clodinafop propargyl 15% WP 80
T9 Haloxyfop-r-methyl 10.5% EC 120
T10 Propaquizafop 10% EC 50
T11 Quizalofop ethyl 10% EC 45
T12 Fenoxaprop-p-ethyl 9.3% EC 100
T13 Fomesafen 12%+Quizalofop ethyl 3% SC 180+45
T14 Untreated Check (UTC) 0
T1 to T5 are novel OD compositions, T6 to T13 are market available products.
Weed flora composition of trial plot: grassy weeds 60% (Echinochloa colona, Eragrostis major, Digitaria spp.), Broad leaf weeds 40% (Commelina communis, Physalis minima, Digera arvensis).
Table 9: Bio efficacy of Novel OD compositions against mixed weed flora infesting Groundnut crop.
Sr.no. Weed control (%) at 15 DAA
observed expected Colby ratio Synergism (Y/N)
T1 96.2 84.7 1.14 Y
T2 100.0 85.6 1.17 Y
T3 100.0 85.5 1.17 Y
T4 98.2 85.0 1.16 Y
T5 98.2 84.9 1.16 Y
T6 46.6
T7 51.4
T8 41.2
T9 44.4
T10 44.2
T11 42.2
T12 41.8
T13 90.4
T14 0.0
All the novel OD compositions (T1 to T5) provides excellent weed control (>98.2%) as compared to conventional treatments (T6 to T13). Weed control (%) was observed higher T4 (98.2%) as compared to T13 (90.4%) at 15 DAA.
Table 10: Phytotoxicity in Groundnut crop.
Sr.no. Yellowing & discoloration (%)
3 DAA 15 DAA 30 DAA
T1 6.33 0.00 0.00
T2 5.67 0.00 0.00
T3 6.00 0.00 0.00
T4 6.33 0.00 0.00
T5 6.67 0.00 0.00
T6 5.67 0.00 0.00
T7 7.33 0.00 0.00
T8 0.00 0.00 0.00
T9 0.00 0.00 0.00
T10 0.00 0.00 0.00
T11 0.00 0.00 0.00
T12 0.00 0.00 0.00
T13 7.33 0.00 0.00
T14 0.00 0.00 0.00
Phytotoxicity was observed in terms of yellowing and discoloration of foliage, which was completely recovered within 15 DAA in treatments T1, T2, T3, T4, T5, T6, T7 and T13. All novel OD compositions (T1 to T5) were found safe to the groundnut crop.
EXPERIMENT-5
Example 5: Bio efficacy comparison of Novel OD compositions comprising of Fluthiacet methyl+Imazethapyr+one more herbicide.
Crop : Soybean
Target weeds : mixed weed flora (Grasses+broadleaf+sedges)
Location : Devas, Madhya Pradesh
Number of Treatments: 15
Plot size : 10 m x 5 m=50 sq.m.
Application time : 15 DAS (days after sowing), 2 to 4 leaf stage of weeds.
Application method : foliar spray with backpack sprayer attached flat fan nozzle.
Water volume : 400 liter per hectare
Observation Methods : Weed control (%) and phytotoxicity, same as per example 1.
Table 11: Treatment details.
Sr.no. Treatment compositions Application Rate (gai/h)
T1 Fluthiacet methyl 1%+Imazethapyr 6%+Clodinafop propargyl 8% OD 10+60+80
T2 Fluthiacet methyl 1%+Imazethapyr 6%+Haloxyfop-r-methyl 12% OD 10+60+120
T3 Fluthiacet methyl 2%+Imazethapyr 12%+Propaquizafop 10% OD 10+60+50
T4 Fluthiacet methyl 2%+Imazethapyr 12%+Quizalofop ethyl 10% OD (Recipe: FIQ) 10+60+50
T5 Fluthiacet methyl 1%+Imazethapyr 6%+Fenoxaprop-p-ethyl 10% OD 10+60+100
T6 Fluthiacet methyl 10.3% EC 10
T7 Imazethapyr 10% SL+ MSO adjuvant @ 2 ml/l water 60
T8 Clodinafop propargyl 15% WP 80
T9 Haloxyfop-r-methyl 10.5% EC 120
T10 Propaquizafop 10% EC 50
T11 Quizalofop ethyl 10% EC 50
T12 Fenoxaprop-p-ethyl 9.3% EC 100
T13 Propaquizafop 2.5%+Imazethapyr 3.75% ME 50+75
T14 Quizalofop ethyl 7.5%+Imazethapyr 15% EC 32.81+65.625
T15 Untreated Check (UTC) 0
T1 to T5 are novel OD compositions, T6 to T14 are market available products.
Weed flora compositions of trial plot: Grassy weeds 45% (Echinochloa crusgallis, Dactyloctenium spp., Digitaria spp.), Broad leaf weeds 45% (Commelina benghalensis, Commelina communis, Digera arvensis, Amaranthus spinoceous, Phyllanthus niruri), Sedges 10% (Cyperus rotundus).
Table 12: Bio efficacy against mixed weed flora in soybean.
Sr.No. Weed control (%) Number of pods per plant Increase (%) in pods per plant over T15
15 DAA 30 DAA
observed Expected Colby ratio Synergism (Y/N)
T1 100.0 88.6 1.13 Y 94.8 55.3 76.11
T2 100.0 88.8 1.13 Y 98.8 57.7 83.76
T3 100.0 88.7 1.13 Y 98.2 57.1 81.85
T4 100.0 88.6 1.13 Y 96.4 56.8 80.89
T5 100.0 88.4 1.13 Y 95.8 56.2 78.98
T6 42.8 40.2 37.9 20.70
T7 64.8 61.6 42.7 35.99
T8 43.2 40.8 38.5 22.61
T9 44.4 41.4 39.8 26.75
T10 43.8 40.2 38.1 21.34
T11 43.6 41.4 39.4 25.48
T12 42.4 39.6 36.8 17.20
T13 89.4 84.6 48.6 54.78
T14 84.2 78.8 46.5 48.09
T15 0.0 0.0 31.4 0.00
All the novel OD compositions comprising Fluthiacet methyl+Imazethapyr+one more herbicide (T1 to T5) provides excellent cent percent weed control at 15 DAA, whereas both the conventional ready mix market available product, T13 provides 89.4% and T14 provides 84.2% weed control. At 30 DAA, all the novel OD compositions provides >94.8% weed control, superior to conventional ready mix market available products (T13 and T14). Pod yield was observed higher (>76.11%) with all the novel OD compositions, whereas it was lower (<54.78%) with conventional ready mix market available products (T13 &T14).
EXPERIMENT-6
Example 6: Bio efficacy comparison of Novel OD compositions comprising of Fluthiacet methyl+Imazamox+one more herbicide.
Crop : Green gram
Target weeds : mixed weed flora (Grasses+broadleaf+sedges)
Location : Karjan, Gujarat
Number of Treatments: 14
Plot size : 8 m x 5 m=40 sq.m.
Application time : 24 DAS (days after sowing), 2 to 4 leaf stage of weeds.
Application method : foliar spray with backpack sprayer attached flat fan nozzle.
Water volume : 400 liter per hectare
Observation Methods : Weed control (%) and phytotoxicity, same as per example 1.
Table 13: Bio efficacy against mixed weed flora in green gram crop.
Treatment compositions Application Rate (gai/h) Weed control (%) at 15 DAA
observed expected Colby ratio Synergism (Y/N)
T1-Fluthiacet methyl 1%+Imazamox 6%+Clodinafop propargyl 8% OD 10+60+80 97.8 87.1 1.12 Y
T2-Fluthiacet methyl 1%+Imazamox 6%+Haloxyfop-r-methyl 12% OD 10+60+120 99.8 87.4 1.14 Y
T3-Fluthiacet methyl 2%+Imazamox 12%+Propaquizafop 10% OD 10+60+50 99.4 87.3 1.14 Y
T4-Fluthiacet methyl 2%+Imazamox 12%+Quizalofop ethyl 9% OD 10+60+45 98.6 87.1 1.13 Y
T5-Fluthiacet methyl 1%+Imazamox 6%+Fenoxaprop-p-ethyl 10% OD 10+60+100 98.2 86.8 1.13 Y
T6-Fluthiacet methyl 10.3% EC 10 53.8
T7-Imazethapyr 10% SL+MSO adjuvant @ 2ml/l water 60 55.2
T8-Clodinafop propargyl 15% WP 80 37.8
T9-Haloxyfop-r-methyl 10.5% EC 120 39.2
T10-Propaquizafop 10% EC 50 38.4
T11-Quizalofop ethyl 10% EC 45 37.6
T12-Fenoxaprop-p-ethyl 9.3% EC 100 36.4
T13-Imazethapyr 35%+Imazamox 35% WG, MSO adjuvant @ 2 ml/l water 70 68.4
T14-Untreated Check (UTC) 0 0.0
T1 to T5 are novel OD compositions, T6 to T13 are market available products.
Weed flora compositions of trial plot: Grassy weeds 40% (Echinochloa colona, Dinebra spp.), Broad leaf weeds 60% (Physalis minima, Trianthema monogyna, Amaranthus viridis, Parthenium hysterophorus).
All the novel OD compositions comprising Fluthiacet methyl+Imazamox+one more herbicide (T1 to T5) provides synergistic weed control and higher efficacy against all weed species.
EXPERIMENT-7
Example 7: Bio efficacy comparison of Novel OD compositions comprising of Fluthiacet methyl+Fomesafen+one more herbicide.
Crop : Black gram
Target weeds : mixed weed flora (Grasses+broadleaf+sedges)
Location : Vijaywada, Andhra Pradesh
Number of Treatments: 20
Plot size : 7 m x 5 m=35 sq.m.
Application time : 21 DAS (days after sowing), 2 to 4 leaf stage of weeds.
Application method : foliar spray with backpack sprayer attached flat fan nozzle.
Water volume : 430 liter per hectare
Observation Methods: Weed control (%) and phytotoxicity, same as per example 1.
Table 14: Treatment details.
Sr.no. Treatment compositions Application Rate (gai/h)
T1 Fluthiacet methyl 1%+Fomesafen 12%+Fluazifop-p-butyl 12% OD 10+120+120
T2 Fluthiacet methyl 1%+Fomesafen 12%+Clethodim 12% OD 10+120+120
T3 Fluthiacet methyl 1%+Fomesafen 12%+Propaquizafop 5% OD 10+120+50
T4 Fluthiacet methyl 1%+Fomesafen 12%+Haloxyfop-r-methyl 12% OD 10+120+120
T5 Fluthiacet methyl 1%+Fomesafen 12% EC 10+120
T6 Fluthiacet methyl 1%+Fluazifop-p-butyl 12% EC 10+120
T7 Fluthiacet methyl 2%+Clethodim 24% EC 10+120
T8 Fluthiacet methyl 2%+Propaquizafop 10% EC 10+50
T9 Fluthiacet methyl 1%+Haloxyfop-r-methyl 12% EC 10+120
T10 Fomesafen 12%+Fluazifop-p-butyl 12% SL 120+120
T11 Fomesafen 12%+Clethodim 12% EC 120+120
T12 Fomesafen 12%+Propaquizafop 5% ME 120+50
T13 Fomesafen 12%+Haloxyfop-r-methyl 12% EC 120+120
T14 Fluthiacet methyl 10.3% EC 10
T15 Sodium salt of Fomesafen 22.1% SL 120
T16 Fluazifop-p-butyl 10% EC 120
T17 Clethodim 25% EC 120
T18 Propaquizafop 10% EC 50
T19 Haloxyfop-r-methyl 10.5% EC 120
T20 Untreated Check (UTC) 0
T1 to T4 are novel OD compositions, T5 to T13 are ready mix conventional treatments, T14 to T19 are market available products.
Weed flora compositions of trial plot: Grassy weeds 50% (Echinochloacrusgalli, Digitaria spp., Dinebra spp.), Broad leaf weeds 50% (Digeraarvensis, Trianthemamonogyna, Amaranthusviridis).
Table 15: Bio efficacy of novel OD compositions against mixed weed flora infesting black gram crop.
Sr.no. Weed control (%)
15 DAA 30 DAA
observed expected Colby ratio Synergism (Y/N)
T1 97.8 83.7 1.17 Y 97.8
T2 98.4 84.1 1.17 Y 98.4
T3 98.8 84.1 1.17 Y 98.8
T4 99.2 84.4 1.18 Y 99.2
T5 83.2 70.1 1.19 Y 83.2
T6 82.6 69.8 1.18 Y 82.6
T7 83.0 70.4 1.18 Y 83.0
T8 83.6 70.5 1.19 Y 83.6
T9 84.8 71.0 1.19 Y 84.8
T10 83.4 70.7 1.18 Y 83.4
T11 85.0 71.4 1.19 Y 85.0
T12 85.6 71.5 1.20 Y 85.6
T13 85.2 71.9 1.18 Y 85.2
T14 44.4 44.4
T15 46.2 46.2
T16 45.6 45.6
T17 46.8 46.8
T18 47.0 47.0
T19 47.8 47.8
T20 0.0 0.0
All the novel OD compositions (T1 to T4) provides synergistic control of mixed flora in black gram crop and provides higher efficacy (in terms of weed control) as compared to all ready-mix conventional treatments (T5 to T13) and market available products (T14 to T19).
EXPERIMENT-8
Example 8: Bio efficacy evaluation of Novel OD (Oil dispersion) compositions comprising of Fluthiacet methyl+Herbicide+Pinoxaden.
Crop : Soybean (Glycine max)
Target weeds : mixed weed flora (Grasses+broadleaf+sedges)
Location : Modasa, Gujarat
Number of Treatments: 11
Plot size : 10 m x 5 m=50 sq.m.
Application time : 19 DAS (days after sowing), 2 to 6 leaf stage of weeds.
Application method : foliar spray with backpack sprayer attached flat fan nozzle.
Water volume : 470 litre per hectare
Observation Methods : Weed control (%) and phytotoxicity, same as per example 1.
Pod counts: Count the number of pods per plant, record the observations from 20 plants per plot at the time of harvest.
Table 16: Treatment details.
Treatment compositions Application Rate (gai/h) Weed control (%) at 15 DAA
observed expected Colby ratio Synergism (Y/N)
T1-Fluthiacet methyl 1.2%+Acifluorfen 12%+Pinoxaden 6% OD 12+120+60 99.4 85.6 1.16 Y
T2-Fluthiacet methyl 1.2%+Fomesafen 12%+Pinoxaden 6% OD 12+120+60 99.2 85.7 1.16 Y
T3-Fluthiacet methyl 2.4%+Chlorimuron ethyl 1.5%+Pinoxaden 12% OD 12+7.5+60 98.6 84.9 1.16 Y
T4-Fluthiacet methyl 1.2%+Imazethapyr 5%+Pinoxaden 6% OD 12+50+60 100.0 86.2 1.16 Y
T5-Fluthiacet methyl 10.3% EC 12 46.2
T6-Pinoxaden 5.1% EC 60 48.4
T7-Sodium salt of Acifluorfen 20.1% SL 120 48.2
T8-Sodium salt of Fomesafen 22.1% SL 120 48.6
T9-Chlorimuron ethyl 25% WP+0.2% Nonionic surfactant 7.5 45.6
T10-Imazethapyr 10% SL+MSO adjuvant @ 2 ml/l water 50 50.2
T11-Untreated Check (UTC) 0 0.0
T1 to T4 are novel OD compositions, T5 to T10 are market products.
All the novel OD compositions (T1 to T4) provides excellent weed control (>98.6%) as compared to conventional treatments (T5 to T10).
EXPERIMENT-9
Experiment 9: Spreading properties study.
Method: Spreading properties test conducted by preparing 1% solution (1 ml formulation in 100 ml water). Drop the solution on leaf surface (Soybean leaf) and measure the spreading diameter (cm) after 30 seconds. Spreading diameter measured by graph paper.
Compositions Room temperature storage
1 month 6 months 12 months
(Spreading diameter in centimetres)
Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% OD (Recipe: FCH-A, Novel OD) 23 22 21
Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% OD (Recipe: FCH-B, conventional OD) 10 9 8
Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% SE (conventional) 10 9 8
Fluthiacet methyl 2.4%+Chlorimuron ethyl 1.5%+Haloxyfop-r-methyl 24% WG (conventional) 6 5 5
The novel OD composition of Fluthiacet methyl 1.2%+Chlorimuron ethyl 0.75%+Haloxyfop-r-methyl 12% OD (Recipe: FCH-A, Novel OD) shows excellent spreading properties. This will improve the bio efficacy under field condition, ensures quick control of target weeds and also improves the rain fast properties during rainy days.
Summary of the biological experiments:
• Novel OD compositions provides quick control and higher efficacy as compared conventional formulations likes OD, EC, SL, SC and tank mixes.
• Excellent synergistic weed control of grassy, broad leaf weeds and sedges.
• Improved bio efficacy against tough to kill weeds.
• Residual weed control.
• Excellent crop safety to soybean, groundnut, green gram and black gram.
• Increases in yield attributing parameters.
,CLAIMS:CLAIMS:
We claim.
[CLAIM 1]. An Oil Dispersion agrochemical composition comprising:
a. Fluthiacet methyl is in the range of 0.5% to 5% w/w.
b. herbicide selected from Chlorimuron ethyl, Imazethapyr, Imazamox, Fomesafen, Lactofen, Aciflurofen, Bentazone or their salt in the range of 0.5% to 40% w/w.
c. at least one more herbicide selected from Clodinafop propargyl, Cyhalofop-butyl, Diclofop, Fenoxaprop-p-ethyl, Fluazifop-p-butyl, Haloxyfop-methyl, Metamifop, Propaquizafop, Quizalofop-p-ethyl, Alloxydim, Butroxydim, Clethodim, Cloproxydim, Cycloxydim, Profoxydim, Sethoxydim, Tepraloxydim, Tralkoxydim, Penoxaden or their salt in the range of 1.0% to 40% w/w composition.
d. a super wetting-spreading-penetrating agent is polyalkylene oxide modified heptamethyl trisiloxane present in an amount of 1% to 20% w/w.
e. carrier solvent selected from pongamia oil, palm oil, jojoba oil or combination thereof or blend thereof with vegetable oil present in an amount of 10% to 80% w/w; and
f. one or more formulation excipients.
[CLAIM 2]. The synergistic Oil Dispersion agrochemical composition as claimed in claim 1, wherein solvent is a carrier oil phase selected from pongamia oil; or palm oil; or pongamia oil and palm oil; or pongamia oil and jojoba oil; or palm oil and jojoba oil; or pongamia oil and vegetable oil; or palm oil and vegetable oil; or pongamia oil and palm oil and vegetable oil; and alkylated or ethoxylated or epoxylated or esterified forms thereof selected from methyl ester of karanj oil, methyl ester of palm oil, methyl ester of karanj oil and soybean oil, methyl ester of palm oil and castor oil, methyl ester of palm oil and rapeseed oil.
[CLAIM 3]. The synergistic Oil Dispersion agrochemical composition as claimed in claim 1, wherein vegetable oil is selected from one or mixture of two or more selected from soybean (Glycine max) oil, groundnut (Arachis hypogaea) oil, rapeseed (Brassica napus subspecies) oil, mustard (Brassica juncea) oil, sesame (Sesamumindicum) oil, Corn (Zea mays) oil, rice (Oryzasativa) bran oil, castor (Ricinumcommunis) seed oil, cotton (Gossypiumhirsutum) seed oil, linseed (Linumusitatissimum), coconut (Cocos nucifera) oil, Kapok (Ceibapentandra) oil, Papaya (Carica papaya) seed oil, Tea seed (Camellia oleifera) oil, sunflower (Helianthus annuus) oil, safflower (Carthamustinctorius) seed oil, Eucalyptus (Eucalyptus globulus) oil, Olive (Oleaeuropaea) oil, Jatropha (Jatropha curcas) oil, Garlic acid (Allium sativum), Ginger oil (Zingiberofficinale), D-limonene, Citronella oil or Ceylon ironwood (Mesuaferrea) oil, Mahua (Madhucalongifolia) oil.
[CLAIM 4]. The synergistic Oil Dispersion agrochemical composition as claimed in claim 1, wherein formulation excipients are selected from category of emulsifying agent present in amount of 2% - 12% w/w; dispersing agent present in amount of 1 % - 10% w/w; stabilizer present in amount of 0.1% - 4 % w/w; antifoaming agent present in amount of 0.01% - 2 % w/w; preservative present in amount of 0.1% - 4 % w/w; anti-freezing agent present in amount of 0.5% - 10 % w/w; optionally buffering agents present in amount of 0.1% - 4 % w/w.
[CLAIM 5]. The synergistic Oil Dispersion agrochemical composition as claimed in claim 4, wherein an emulsifying agent is selected from castor oil ethoxylates, alcohol ethoxylates, fatty acid ethoxylates, sorbitan ester ethoxylates, sulphosuccinate, calcium salts of dodecylbenzene sulphonate, alkylammonium salts of alkylbenzene sulphonate, alkylsulphosuccinate salts, ethylene oxide-propylene oxide block copolymers, ethoxylatedalkylamines, ethoxylated alkyl phenols, polyoxyethylenesorbitanmonolaurate.
[CLAIM 6]. The synergistic Oil Dispersion agrochemical composition as claimed in claim 4, wherein dispersing agent is selected from preparation of condensed naphthalene sulfonate, PropoxylatedEthoxylated copolymer monoalkylether (ethylhexanol), alkyl sulfonates, alkyl benzene sulfonates, alkyl aryl sulfonates, alkylphenolalkoxylates, tristyrylphenolethoxylates, natural or synthetic fatty ethoxylate alcohols, natural or synthetic fatty acid alkoxylates, natural or synthetic fatty alcohols alkoxylates, alkoxylated alcohols (such as n-butyl alcohol poly glycol ether), block copolymers (such as ethylene oxide-propylene oxide block copolymers and ethylene oxide-butylene oxide block copolymers), fatty acid-polyalkylene glycol condensates, polyamine-fatty acid condensates, polyester condensates, salts of polyolefin condensates, sodium ligno sulfonate, sodium ploycarboxylate, EO/PO based copolymer, phenol sulfonate, sodium methyl oleoyltaurate, acrylic copolymer blend, styrene acrylic acid copolymer, propyleneoxide-ethyleneoxide-copolymer, polyethylene glycol 2,4,6-tristyrylphenyl ether, tristyrylphenol-polyglycolether-phosphate, tristyrylphenole with 16 moles EO, tristyrylphenol-polyglycolether-phosphate, oleyl-polyglycolether with ethylene oxide, tallow fattyamine polyethylene oxide, nonylphenolpolyglycolether with 9-10 moles ethylene oxide.
[CLAIM 7]. The synergistic Oil Dispersion agrochemical composition as claimed in claim 4, wherein stabilizer is selected from hectorite clay, aluminium magnesium silicate, bentonite clay, silica, silicon dioxide, attapulgite clay.
[CLAIM 8]. The synergistic Oil Dispersion agrochemical composition as claimed in claim 4, wherein antifoaming agent is selected from silicone oil, silicone compound, C10~C20 saturated fat acid compounds or C8~C10 aliphatic alcohols compound, silicone antifoam emulsion, dimethylsiloxane, polydimethyl siloxane.
[CLAIM 9]. The synergistic Oil Dispersion agrochemical composition as claimed in claim 4, wherein anti-freezing agent is selected from ethylene glycol, propane diols, glycerine or the urea, glycol (Monoethylene glycol, Diethylene glycol, Propylene glycol, Polypropylene glycol, Polyethylene glycol), glycerine, urea, magnesium sulfate heptahydrate, sodium chloride.
[CLAIM 10]. The synergistic Oil Dispersion agrochemical composition as claimed in claim 4, wherein preservative is selected from 1,2-benzisothiazolin-3(2H)-one, sodium salt, sodium benzoate, 2-bromo-2-nitropropane-1,3-diol, formaldehyde, sodium o-phenylphenate, 5-chloro-2-methyl-4-isothiazolin-3-one & 2-methyl-4-isothiazolin-3-one, Butyl hydroxyl toluene.
[CLAIM 11]. The synergistic Oil Dispersion agrochemical composition as claimed in claim 4, wherein optionally buffering agent is selected Citric acid, sodium carbonate, sodium bicarbonate, sulphuric acid, hydrochloric acid, sodium hydroxide, potassium hydroxide, acetic acid, sorbic acid.
Dated this 30th day of May 2023
| # | Name | Date |
|---|---|---|
| 1 | 202221030928-STATEMENT OF UNDERTAKING (FORM 3) [30-05-2022(online)].pdf | 2022-05-30 |
| 2 | 202221030928-PROVISIONAL SPECIFICATION [30-05-2022(online)].pdf | 2022-05-30 |
| 3 | 202221030928-POWER OF AUTHORITY [30-05-2022(online)].pdf | 2022-05-30 |
| 4 | 202221030928-FORM FOR SMALL ENTITY(FORM-28) [30-05-2022(online)].pdf | 2022-05-30 |
| 5 | 202221030928-FORM FOR SMALL ENTITY [30-05-2022(online)].pdf | 2022-05-30 |
| 6 | 202221030928-FORM 1 [30-05-2022(online)].pdf | 2022-05-30 |
| 7 | 202221030928-EVIDENCE FOR REGISTRATION UNDER SSI(FORM-28) [30-05-2022(online)].pdf | 2022-05-30 |
| 8 | 202221030928-EVIDENCE FOR REGISTRATION UNDER SSI [30-05-2022(online)].pdf | 2022-05-30 |
| 9 | 202221030928-DECLARATION OF INVENTORSHIP (FORM 5) [30-05-2022(online)].pdf | 2022-05-30 |
| 10 | 202221030928-FORM-9 [30-05-2023(online)].pdf | 2023-05-30 |
| 11 | 202221030928-ENDORSEMENT BY INVENTORS [30-05-2023(online)].pdf | 2023-05-30 |
| 12 | 202221030928-CORRESPONDENCE-OTHERS [30-05-2023(online)].pdf | 2023-05-30 |
| 13 | 202221030928-COMPLETE SPECIFICATION [30-05-2023(online)].pdf | 2023-05-30 |
| 14 | 202221030928-MSME CERTIFICATE [07-06-2023(online)].pdf | 2023-06-07 |
| 15 | 202221030928-FORM28 [07-06-2023(online)].pdf | 2023-06-07 |
| 16 | 202221030928-FORM 18A [07-06-2023(online)].pdf | 2023-06-07 |
| 17 | 202221030928-FER.pdf | 2023-08-22 |
| 18 | 202221030928-OTHERS [22-02-2024(online)].pdf | 2024-02-22 |
| 19 | 202221030928-FER_SER_REPLY [22-02-2024(online)].pdf | 2024-02-22 |
| 20 | 202221030928-US(14)-HearingNotice-(HearingDate-04-04-2024).pdf | 2024-03-18 |
| 21 | 202221030928-Correspondence to notify the Controller [31-03-2024(online)].pdf | 2024-03-31 |
| 22 | 202221030928-NBA Approval Submission [08-04-2024(online)].pdf | 2024-04-08 |
| 23 | 202221030928-Written submissions and relevant documents [19-04-2024(online)].pdf | 2024-04-19 |
| 24 | 202221030928-PETITION UNDER RULE 137 [19-04-2024(online)].pdf | 2024-04-19 |
| 25 | 202221030928-FORM-26 [19-04-2024(online)].pdf | 2024-04-19 |
| 26 | 202221030928-Annexure [19-04-2024(online)].pdf | 2024-04-19 |
| 27 | 202221030928-PatentCertificate28-05-2024.pdf | 2024-05-28 |
| 28 | 202221030928-IntimationOfGrant28-05-2024.pdf | 2024-05-28 |
| 1 | SearchStrategyE_21-08-2023.pdf |