AU2022266180A1 - Soluble liquid compositions comprising flonicamid and uses thereof - Google Patents
Soluble liquid compositions comprising flonicamid and uses thereof Download PDFInfo
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- AU2022266180A1 AU2022266180A1 AU2022266180A AU2022266180A AU2022266180A1 AU 2022266180 A1 AU2022266180 A1 AU 2022266180A1 AU 2022266180 A AU2022266180 A AU 2022266180A AU 2022266180 A AU2022266180 A AU 2022266180A AU 2022266180 A1 AU2022266180 A1 AU 2022266180A1
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- 239000000203 mixture Substances 0.000 title claims abstract description 132
- 239000005900 Flonicamid Substances 0.000 title claims abstract description 74
- RLQJEEJISHYWON-UHFFFAOYSA-N flonicamid Chemical compound FC(F)(F)C1=CC=NC=C1C(=O)NCC#N RLQJEEJISHYWON-UHFFFAOYSA-N 0.000 title claims abstract description 74
- 239000007788 liquid Substances 0.000 title abstract description 10
- 239000002671 adjuvant Substances 0.000 claims abstract description 57
- 239000002904 solvent Substances 0.000 claims abstract description 46
- 239000002917 insecticide Substances 0.000 claims abstract description 27
- 241000607479 Yersinia pestis Species 0.000 claims abstract description 23
- 241001124076 Aphididae Species 0.000 claims abstract description 16
- 241000238631 Hexapoda Species 0.000 claims abstract description 15
- 241001465977 Coccoidea Species 0.000 claims abstract description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 60
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims description 43
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 239000000463 material Substances 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 15
- 241000196324 Embryophyta Species 0.000 claims description 14
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical group CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 claims description 13
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 13
- 229920000151 polyglycol Polymers 0.000 claims description 13
- 239000010695 polyglycol Substances 0.000 claims description 13
- -1 sorbitan ester Chemical class 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 12
- 239000002202 Polyethylene glycol Substances 0.000 claims description 10
- 239000002518 antifoaming agent Substances 0.000 claims description 10
- 229920001223 polyethylene glycol Polymers 0.000 claims description 10
- 150000001336 alkenes Chemical class 0.000 claims description 8
- 238000009835 boiling Methods 0.000 claims description 8
- 238000007037 hydroformylation reaction Methods 0.000 claims description 8
- 150000005215 alkyl ethers Chemical class 0.000 claims description 6
- 125000003368 amide group Chemical group 0.000 claims description 6
- 150000001408 amides Chemical class 0.000 claims description 6
- 239000000839 emulsion Substances 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- 240000002791 Brassica napus Species 0.000 claims description 4
- 235000006008 Brassica napus var napus Nutrition 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000013530 defoamer Substances 0.000 claims description 4
- 239000002480 mineral oil Substances 0.000 claims description 4
- 235000010446 mineral oil Nutrition 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 229920005628 alkoxylated polyol Polymers 0.000 claims description 3
- 235000013399 edible fruits Nutrition 0.000 claims description 3
- ZQTYRTSKQFQYPQ-UHFFFAOYSA-N trisiloxane Chemical compound [SiH3]O[SiH2]O[SiH3] ZQTYRTSKQFQYPQ-UHFFFAOYSA-N 0.000 claims description 3
- JQRXTVACLHSVTF-UHFFFAOYSA-N 3-(2-methoxyethoxy)propyl-methyl-bis(trimethylsilyloxy)silane Chemical compound COCCOCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C JQRXTVACLHSVTF-UHFFFAOYSA-N 0.000 claims description 2
- 235000007319 Avena orientalis Nutrition 0.000 claims description 2
- 244000075850 Avena orientalis Species 0.000 claims description 2
- 244000045195 Cicer arietinum Species 0.000 claims description 2
- 235000010523 Cicer arietinum Nutrition 0.000 claims description 2
- 241000207199 Citrus Species 0.000 claims description 2
- 240000007154 Coffea arabica Species 0.000 claims description 2
- 229920000742 Cotton Polymers 0.000 claims description 2
- 244000068988 Glycine max Species 0.000 claims description 2
- 235000010469 Glycine max Nutrition 0.000 claims description 2
- 241000219146 Gossypium Species 0.000 claims description 2
- 244000020551 Helianthus annuus Species 0.000 claims description 2
- 235000003222 Helianthus annuus Nutrition 0.000 claims description 2
- 240000005979 Hordeum vulgare Species 0.000 claims description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 claims description 2
- 235000014647 Lens culinaris subsp culinaris Nutrition 0.000 claims description 2
- 241000220225 Malus Species 0.000 claims description 2
- 235000011430 Malus pumila Nutrition 0.000 claims description 2
- 235000015103 Malus silvestris Nutrition 0.000 claims description 2
- 235000018290 Musa x paradisiaca Nutrition 0.000 claims description 2
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- 235000010627 Phaseolus vulgaris Nutrition 0.000 claims description 2
- 240000000111 Saccharum officinarum Species 0.000 claims description 2
- 235000007201 Saccharum officinarum Nutrition 0.000 claims description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 2
- 244000061456 Solanum tuberosum Species 0.000 claims description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 claims description 2
- 235000015505 Sorghum bicolor subsp. bicolor Nutrition 0.000 claims description 2
- 235000011684 Sorghum saccharatum Nutrition 0.000 claims description 2
- 244000062793 Sorghum vulgare Species 0.000 claims description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 2
- 235000021307 Triticum Nutrition 0.000 claims description 2
- 244000098338 Triticum aestivum Species 0.000 claims description 2
- 235000020971 citrus fruits Nutrition 0.000 claims description 2
- 235000016213 coffee Nutrition 0.000 claims description 2
- 235000013353 coffee beverage Nutrition 0.000 claims description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 2
- 230000002209 hydrophobic effect Effects 0.000 claims description 2
- ZPIRTVJRHUMMOI-UHFFFAOYSA-N octoxybenzene Chemical compound CCCCCCCCOC1=CC=CC=C1 ZPIRTVJRHUMMOI-UHFFFAOYSA-N 0.000 claims description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- 235000009566 rice Nutrition 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 239000010703 silicon Substances 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims description 2
- YEBLAXBYYVCOLT-UHFFFAOYSA-N 2-hydroxy-n,n-dimethylpropanamide Chemical compound CC(O)C(=O)N(C)C YEBLAXBYYVCOLT-UHFFFAOYSA-N 0.000 claims 1
- 244000043158 Lens esculenta Species 0.000 claims 1
- 240000008790 Musa x paradisiaca Species 0.000 claims 1
- 238000009472 formulation Methods 0.000 description 51
- 239000000047 product Substances 0.000 description 46
- 238000011282 treatment Methods 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 8
- 230000001276 controlling effect Effects 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 229920000136 polysorbate Polymers 0.000 description 6
- 230000009471 action Effects 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000013065 commercial product Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 241000254127 Bemisia tabaci Species 0.000 description 3
- 241000258937 Hemiptera Species 0.000 description 3
- 239000003905 agrochemical Substances 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 2
- 241000238876 Acari Species 0.000 description 2
- 241001109971 Bactericera cockerelli Species 0.000 description 2
- 240000008067 Cucumis sativus Species 0.000 description 2
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 2
- 241001222563 Empoasca onukii Species 0.000 description 2
- 241000501345 Lygus lineolaris Species 0.000 description 2
- 206010034133 Pathogen resistance Diseases 0.000 description 2
- 241000365764 Scirtothrips dorsalis Species 0.000 description 2
- 241000018137 Trialeurodes vaporariorum Species 0.000 description 2
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000004634 feeding behavior Effects 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- LCEDQNDDFOCWGG-UHFFFAOYSA-N morpholine-4-carbaldehyde Chemical compound O=CN1CCOCC1 LCEDQNDDFOCWGG-UHFFFAOYSA-N 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- BNXZHVUCNYMNOS-UHFFFAOYSA-N 1-butylpyrrolidin-2-one Chemical compound CCCCN1CCCC1=O BNXZHVUCNYMNOS-UHFFFAOYSA-N 0.000 description 1
- 241001167029 Amrasca biguttula Species 0.000 description 1
- 241001600408 Aphis gossypii Species 0.000 description 1
- 241000238421 Arthropoda Species 0.000 description 1
- 241001302798 Bemisia argentifolii Species 0.000 description 1
- 241001498622 Cixius wagneri Species 0.000 description 1
- 206010010904 Convulsion Diseases 0.000 description 1
- 241001583841 Empoasca decipiens Species 0.000 description 1
- 108090000371 Esterases Proteins 0.000 description 1
- 241000256244 Heliothis virescens Species 0.000 description 1
- 241000446313 Lamella Species 0.000 description 1
- 240000004322 Lens culinaris Species 0.000 description 1
- 241001599018 Melanogaster Species 0.000 description 1
- 240000005561 Musa balbisiana Species 0.000 description 1
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 description 1
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 description 1
- 241001556089 Nilaparvata lugens Species 0.000 description 1
- 241000819999 Nymphes Species 0.000 description 1
- 241000238675 Periplaneta americana Species 0.000 description 1
- 208000005374 Poisoning Diseases 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 239000005925 Pymetrozine Substances 0.000 description 1
- 108010052164 Sodium Channels Proteins 0.000 description 1
- 102000018674 Sodium Channels Human genes 0.000 description 1
- 241001481304 Vespoidea Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical compound CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 description 1
- 229960004373 acetylcholine Drugs 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000000540 analysis of variance Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 235000021329 brown rice Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 230000036461 convulsion Effects 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- MHPUGCYGQWGLJL-UHFFFAOYSA-N dimethyl pentanoic acid Natural products CC(C)CCCC(O)=O MHPUGCYGQWGLJL-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 231100000673 dose–response relationship Toxicity 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- SXQFCVDSOLSHOQ-UHFFFAOYSA-N lactamide Chemical compound CC(O)C(N)=O SXQFCVDSOLSHOQ-UHFFFAOYSA-N 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000001543 one-way ANOVA Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000000447 pesticide residue Substances 0.000 description 1
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical group NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- QHMTXANCGGJZRX-WUXMJOGZSA-N pymetrozine Chemical compound C1C(C)=NNC(=O)N1\N=C\C1=CC=CN=C1 QHMTXANCGGJZRX-WUXMJOGZSA-N 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000012865 response to insecticide Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P7/00—Arthropodicides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
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- Life Sciences & Earth Sciences (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Insects & Arthropods (AREA)
- Agronomy & Crop Science (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The present invention provides an insecticide liquid stable composition comprising high concentration of flonicamid dissolved in a particular solvent system, and optionally one or more particular adjuvants, which is useful in controlling pest such as insects including an aphid, a mealybug, and a white fly.
Description
SOLUBLE LIQUID COMPOSITIONS COMPRISING FLONICAMID AND USES
THEREOF
TECHNICAL FIELD
[0001] The present invention provides an insecticide liquid stable composition comprising high concentration of flonicamid dissolved in a particular solvent system, and optionally one or more particular adjuvants, which is useful in controlling pest such as insects.
BACKGROUND ART
[0002] The extensive use of conventional insecticides (organochlorines, organophosphates, carbamates, and synthetic pyrethroids) has resulted in the development of severe pest resistance to insecticides, outbreaks of secondary pests, objectionable pesticide residues, direct hazard to the users, and adverse effect on environment and non target organisms.
[0003] New insecticides, having good controlling properties of insect pests at low rates or doses, high level of selectivity, and greater specificity to target pests along with low toxicity to non-target organisms and the environment, replaced many old/conventional compounds. Such compounds are also less likely to cause outbreaks of secondary pests, extremely helpful for delaying resistance in key pests such as whiteflies and aphids, and have no cross-resistance with the old and already established insecticides (Kodandaram el al, 2010).
[0004] For instance, flonicamid (A-(cyanomethyl)-4-(trifluoromethyl)pyridine-3- carboxamide) is a highly selective insecticide belonging to the pyridine carboxamide group. Although it does not control coleopteran, lepidopteran, or dipteran insects and mites, it is effective against both nymph and adult stages of aphids. At the recommended doses under field conditions (50-100 gram active ingredient/hectare or 2.5-10 gram/100 L), this compound is highly effective in controlling a broad range of aphid species as well as other species of sucking insects such as greenhouse whitefly ( Trialeurodes vaporariorum ), yellow tea thrips ( Scirtothrips dorsalis ), Indian cotton leafhopper ( Amrasca biguttula), tea green leafhopper ( Empoasca onukii), tarnished plant bug ( Lygus lineolaris ), potato psyllid (Bactericera cocker elli), and brown rice planthopper ( Nilaparvata lugens), while at the same time it does not negatively impact beneficial arthropods such as predatory mites,
parasitic wasps, predatory insects, and pollinators. Specifically, within 30 minutes after treatment, this compound inhibits the feeding behavior of aphids without noticeable poisoning symptoms such as convulsions or knockdown.
[0005] The precise mechanism of action of flonicamid is under investigation, yet it is clearly different from any conventional one, and its mode of action is different from other insecticides such as neonicotinoids, pymetrozine, and pyri-uquinazon. Actually, flonicamid exhibits no response against the existing insecticide targets such as acetylcholine esterase, and the sodium channel. In addition, although sharing structural similarities with neonicotinoid insecticides, flonicamid has no effect on nicotinic acetylcholine receptors from Periplaneta americana, D. melanogaster, or Heliothis virescens as well (Morita et al, 2007).
[0006] Currently, flonicamid is the only insecticide that belongs to Insecticide Resistance Action Committee (IRAC) Group 29 with an undefined target site of action. It rapidly inhibits the feeding behavior of aphids, and has better action through ingestion than by contact.
[0007] Leaf dip assays in the laboratory showed that flonicamid is highly effective against every 15 field clones of Aphis gossypii tested, while having no cross-resistance to conventional insecticides such as organophosphates, carbamates, or pyrethroids. Flonicamid showed a long-lasting efficacy, controlling aphids for three to four weeks at 50 ppm. It possesses excellent translaminar and systemic activity through xylem vessels (Morita et al., 2014).
[0008] Most of the currently available flonicamid-based products are solid formulations in the form of wettable or soluble granules (comprising 500 g/kg flonicamid); however, the main problem associated with using such solid formulations is the dust which is formed within the product-containing package prior to use.
[0009] As previously published (Ren et al, 2018), flonicamid is soluble in anhydrous dimethyl sulfoxide (DMSO). Yet, and as in fact shown by the present inventors, DMSO- based formulations containing high concentration, e.g., about 22.5% by weight, of flonicamid freeze at low temperatures (e.g., at a temperature of -10°C) due to the melting point of DMSO (19°C).
SUMMARY OF INVENTION
[0010] It has now been found, in accordance with the present invention, that flonicamid in high concentrations dissolve in a particular solvent system consisting of DMSO and an additional solvent selected from Rhodiasolv® PolarClean (Rhodia Poliamida e Especialidades Ltd.), N-butyl-2-pyrrolidonc (NBP), and Agnique® AMD 3L (BASF) to thereby form highly stable soluble liquid (SL) formulations comprising high concentrations, e.g., from about 15% to about 30% by weight, of said insecticide. Such SL formulations maintain their stability even after the addition of one or more particular agriculturally acceptable adjuvants, wherein the adjuvant-containing formulations obtained are highly effective in controlling insects such as tobacco whiteflies.
[0011] For example, a particular such formulation comprising 22.3% by weight flonicamid, dissolved in a solvent system consisting of DMSO and Rhodiasolv® PolarClean at a weight ratio of 1:1.6, respectively, was shown to be stable at room temperature as well as at a lower temperature of up to -10°C, and after the addition of an adjuvant, more specifically Lutensol® TO 8 (BASF), Atplus™ UEP-100 (Croda Crop Care), Silwet® L-77 (Momentive), or Tween 24, in an amount of 22.3% by weight, was found to be more effective, i.e., showed higher percentage in adult Bemicia tabaci mortality 72 hours after application to whole plants, as compared to the commercially available product Teppeki® (comprising wettable granules containing 500 g/kg flonicamid).
[0012] In one aspect, the present invention thus provides an insecticide composition comprising flonicamid in an amount of from about 15% to about 30%, preferably from about 20% to about 27%, by weight; and a solvent system (also referred to herein as a solvent combination) comprising DMSO and an additional solvent selected from pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo-methyl ester, N-(C1-C8)alkyl pyrrolidone, preferably N-(C1-C8)alkyl-2-pyrrolidonc, an amide of the formula R-C(0)-N(CH3)2, wherein R is (Ci-Ci2)alkyl optionally substituted, preferably at position a to the amide group, with a group selected from -OH, -0-(Ci-C6)alkyl, -CN, and -NO2, a commercially available product comprising (e.g., consisting essentially of) it, and a mixture thereof. [0013] In certain embodiments, said solvent system comprises DMSO and an additional solvent selected from pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo-methyl ester; NBP; N,N-dimcthyl lactamide; a commercially available product comprising, or consisting
essentially of, pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo-methyl ester, NBP, or N,N-di methyl lactamide; or a mixture thereof.
[0014] In a particular such aspect, said insecticide composition further comprises at least one adjuvant each independently selected from an alcohol ethoxylate, a sorbitan ester alkoxylate, an alkoxylated polyol ester, a trisiloxane ethoxylate, and a commercially available product comprising it; and optionally an anti-foaming agent, wherein preferred such compositions comprise, as said adjuvant, isotridecanol polyglycol ether 8 ethylene oxide or a commercially available product comprising it (e.g., Lutensol® TO 8), or a mixture of polyethylene glycol (Cii-C 14) alkyl ethers enriched therewith or a commercially available product comprising it (e.g., Genapol® X-080).
[0015] In other aspects, the present invention relates to methods for using insecticide compositions as defined above, i.e., SL formulations containing high concentrations of flonicamid. In one particular such aspect, disclosed herein is a method of controlling pest, such as an insect, comprising applying to a locus where control of said pest is desired, such as a field of crop, an effective amount of an insecticide composition as defined herein. In another particular such aspect, disclosed herein is a method for the protection of a plant propagation material from an attack by a pest such as an insect, comprising treating the propagation material or the site where the propagation material is to be planted with an effective amount of an insecticide composition as defined herein.
BRIEF DESCRIPTION OF DRAWINGS
[0016] Fig. 1 shows aphids’ mortality (%) 72 hours post treatment with several flonicamid-based formulations (SL250) comprising various build-in adjuvants or mixed with tank mix adjuvants as compared to the commercial product Teppeki®, at two application rates (5 and 25 ppm) performed on detached cucumber leaves.
[0017] Fig. 2 shows the biological efficacy (dose response) of various flonicamid (25 ppm)-based SL formulations having different ratios of Silwet® L-77 adjuvant (flonicamid:adjuvant 1:0.25-1) as compared to the commercial product Teppeki® on aphids’ mortality (%) 72 hours post treatment.
DETAILED DESCRIPTION
[0018] In one aspect, disclosed herein is a composition comprising: (a) flonicamid as an insecticide, in an amount of from about 15% to about 30%, preferably from about 20% to
about 27%, by weight; and (b) a solvent system comprising DMSO and an additional agriculturally acceptable solvent selected from pentanoic acid 5-(dimethylamino)-2- methyl-5-oxo-methyl ester; N-(C1-C8)alkyl pyrrolidone; an amide of the formula R-C(O)- N(C¾)2, wherein R is (Ci-Ci2)alkyl optionally substituted, preferably at position a to the amide group, with a group selected from -OH, -0-(Ci-C6)alkyl, -CN, and -NO2; a commercially available product comprising said pentanoic acid 5-(dimethylamino)-2- methyl-5-oxo-methyl ester, said N-(C1-C8)alkyl pyrrolidone, or said amide of the formula R-C(0)-N(CH3)2; and a mixture thereof.
[0019] The term "alkyl" typically means a linear or branched hydrocarbyl having, e.g., 1- 12 carbon atoms and includes, e.g., methyl, ethyl, //-propyl, isopropyl, 77-butyl, sec-butyl, isobutyl, tert-butyl, 77-pentyl, 2,2-dimethylpropyl, 77-hexyl, 77-heptyl, 77-octyl, and the like. Preferred are (C1-C8)alkyls or (Ci-C6)alkyls, more preferably methyl, ethyl, propyl, isopropyl, butyl, and tert-butyl. The alkyl may optionally be substituted by one or more groups (substituents) each independently selected from, e.g., -OH, -0-(Ci-C6)alkyl, -CN, and -NO2.
[0020] Particular solvents of the formula N-(C1-C8)alkyl pyrrolidone referred to herein are those of the formula A/-(C1-C8)alkyl-2-pyrrolidone, preferably wherein said alkyl is (Ci-C4)alkyl, e.g., NBP (wherein said alkyl is butyl).
[0021] Particular solvents of the formula R-C(0)-N(CH3)2 referred to herein are those wherein group R is (Ci-COalkyl, e.g., methyl, ethyl, propyl, or butyl, substituted at any carbon atom thereof with one or more groups each independently selected from -OH, -O- (Ci-C6)alkyl, -CN, and -NO2, but preferably with one of said groups, e.g., -OH, at position a to the amide group, such as N,N-di methyl lactamide.
[0022] In certain embodiments, the additional solvent composing, together with DMSO, the solvent system referred to herein, is a compound as defined above, i.e., pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo-methyl ester; N-(C1-C8)alkyl pyrrolidone, preferably N-(C1-C8)alkyl-2-pyrrolidonc such as NBP; or an amide of the formula (Ci-Ci2)alkyl- C(0)-N(CH3)2 optionally substituted at the alkyl group, preferably at position a to the amide group, with a group as defined above, e.g., N,N-di methyl lactamide, a commercially available product consisting essentially of said compound, or a mixture thereof. The term "consisting essentially of" as used herein with respect to said commercially available product means that said product comprises at least 90%, e.g., at least about 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99%, by weight, of said compound, such that any
other material if included within said solvent does not affect the basic physical and chemical properties of said compound.
[0023] The term “solvent system” or “solvent combination”, used herein interchangeably, thus refers to a combination of two or more solvents, wherein one of said solvents is DMSO, and the other solvent is a compound selected from pentanoic acid 5- (dimethylamino)-2-methyl-5-oxo-methyl ester, N-(C1-C8)alkyl pyrrolidone, preferably N- (C1-C8)alkyl-2-pyrrolidone, and an amide of the formula (Ci-Ci2)alkyl-C(0)-N(CH3)2 optionally substituted at the alkyl group, preferably at position a to the amide group, with a group selected from -OH, -0-(Ci-C6)alkyl, -CN, and -NO2; a commercially available product comprising, e.g., at least 90%, but preferably at least about 92%, 94%, 96%, 98%, or 99%, by weight, i.e., consisting essentially of, one of said compounds; and a mixture thereof. Examples of commercially available products consisting essentially of pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo-methyl ester include, e.g., Rhodiasolv® PolarClean; and examples of commercially available products consisting essentially of A, A-di methyl lactamide include, e.g., Agnique® AMD 3L.
[0024] As shown herein, such a solvent system, e.g., a solvent combination comprising DMSO and Rhodiasolv® PolarClean at a weight ratio of about 1:1.6, respectively, is capable of dissolving high concentrations of flonicamid and to form a soluble liquid flonicamid formulation that is stable at both room temperature and freezing conditions (- 10°C).
[0025] In certain embodiments, the ratio between the DMSO and the additional solvent(s) composing the solvent system referred to herein is from about 2:1 to about 1:4, e.g., about 1.8:1, about 1.6:1, 1.4:1, 1.2:1, about 1:1, about 1:1.2, about 1:1.4, about 1:1.5, about 1:1.6, about 1:1.75, about 1:1.8, about 1:2, about 1:2.2, about 1:2.4, about 1:2.6, about 1:2.8, about 1:3, about 1:3.2, about 1:3.4, about 1:3.6, or about 1:3.8, respectively, by weight.
[0026] In certain embodiments, the solvent system referred to herein comprises DMSO and pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo-methyl ester or a commercially available product comprising, or consisting essentially of, pentanoic acid 5- (dimethylamino)-2-methyl-5-oxo-methyl ester (e.g., Rhodiasolv® PolarClean), as an additional solvent. In particular such embodiments, the ratio between the DMSO and the additional solvent is from about 2:1 to about 1:4, e.g., about 1.8:1, about 1.6:1, 1.4:1, 1.2:1, about 1:1, about 1:1.2, about 1:1.4, about 1:1.5, about 1:1.6, about 1:1.75, about 1:1.8,
about 1:2, about 1:2.2, about 1:2.4, about 1:2.6, about 1:2.8, about 1:3, about 1:3.2, about 1:3.4, about 1:3.6, or about 1:3.8, respectively, by weight.
[0027] In certain embodiments, the composition of the invention according to any one of the embodiments defined above further comprises at least one, e.g., two, three, four, or more, adjuvant each independently selected from an alcohol ethoxylate or a commercially available product comprising it, such as a polyethylene glycol (Cii-C 14) alkyl ether, e.g., isotridecanol polyglycol ether 8 ethylene oxide (e.g., Lutensol® TO 8), or a mixture of polyethylene glycol (C11-C14)alkyl ethers enriched therewith (e.g., Genapol® X-080), and polyethylene glycol octylphenyl ether (e.g., Triton™ X-100); a sorbitan ester alkoxylate or a commercially available product comprising it, such as Tween 20, Tween 21, Tween 22, Tween 23, Tween 24, and Tween 28; an alkoxylated polyol ester or a commercially available product comprising it, such as an ester of (C18)unsaturated fatty acid with a polyethylene glycol ether with trimethylolpropane (3:1) (e.g., Atplus™ UEP-100); and a trisiloxane ethoxylate or a commercially available product comprising it, such as 3-(2- methoxyethoxy)propyl-methyl-bis(trimethylsilyloxy) silane (e.g., Silwet® L-77) (referred to herein as “SL flonicamid-adjuvant-based composition").
[0028] Adjuvants are auxiliaries, which are added to agricultural compositions so as to increase the effectiveness of one or more of the agrochemical agents comprised therein, e.g., a herbicide, insecticide, and/or fungicide. The increase in the efficacy of said agrochemical agent induced by the presence of said adjuvant may be due to several possible modes of action such as facilitated wetting, penetration, or better retention. Adjuvants added to a spray liquid in a tank before application are called "tank-mix adjuvants", and adjuvants incorporated within the formulation as provided are called "built-in” or “in-can adjuvants”.
[0029] In particular such embodiments, the at least one adjuvant comprised within the composition of the invention each independently is isotridecanol polyglycol ether 8 ethylene oxide or a commercially available product comprising it (e.g., Lutensol® TO 8), or a mixture of polyethylene glycol (C11-C14)alkyl ethers enriched therewith or a commercially available product comprising it (e.g., Genapol® X-080). More specific such compositions are those comprising isotridecanol polyglycol ether 8 ethylene oxide or a commercially available product comprising it (e.g., Lutensol® TO 8) as the adjuvant.
[0030] In certain embodiments, the insecticide composition disclosed herein comprises a solvent system as defined above, and at least one adjuvant as defined in any one of the
embodiments above, e.g., isotridecanol polyglycol ether 8 ethylene oxide or a commercially available product comprising it (e.g., Lutensol® TO 8). Particular such compositions are those wherein the ratio between the flonicamid and the adjuvant in said composition is from about 1:0.5 to about 1:2, e.g., from about 1:0.7 to about 1:1.5, from about 1:0.8 to about 1:1.4, from about 1:0.9 to about 1:1.3, from about 1:1 to about 1:1.2, or about 1:1, respectively, by weight. More particular such compositions are those wherein the solvent system comprises DMSO in an amount of from about 17% to about 27%, preferably from about 20% to about 24%, or about 21.5%, by weight, and pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo-methyl ester or a commercially available product comprising (or consisting essentially of) it (e.g., Rhodiasolv® PolarClean), in an amount of from about 25% to about 40%, preferably from about 27% to about 37%, from about 30% to about 35%, or about 32%, by weight.
[0031] In certain embodiments, the SL flonicamid-adjuvant-based composition of the invention, as defined according to any one of the embodiments above, further comprises an anti-foaming agent.
[0032] The term “anti-foaming agent” or “defoamer” as used herein interchangeably refers to a chemical agent that is added to a composition so as to prevent, attenuate, or counter foam generation in the composition. Generally, such agents have surface active properties, are insoluble in the foaming medium, easily spreadable on the foamy surface, possess affinity to the air-liquid surface, and destabilize the foam lamellas which rupture the air bubbles and break down the surface foam.
[0033] Non-limiting examples of anti-foaming agents include a mixture of alkenes, Cn- Ci2, hydroformylation products, low boiling, or a commercially available product comprising it such as Geronol AF 80; a mineral oil-based defoamer or a commercially available product comprising it such as Lucrafoam® PDT; a blend of special wax, hydrophobic silica, and mineral oil or a commercially available product comprising it such as DEE FO® 3010E/50; a silicon emulsion or a commercially available product comprising it such as Silfoam® SE 47, Silfoam® SRE, Silcolapse® RG 12, and SAG 1572; a polydimethyl siloxane emulsion or a commercially available product comprising it such as SAG 10E; and a silicone-based compound or a commercially available product comprising it such as Silcolapse™ 910 and Xiameter® ACP-1000.
[0034] In certain embodiments, the anti-foaming agent comprised within the composition of the invention constitutes from about 0.5% to about 3%, e.g., from about
0.75% to about 2.5%, from about 1% to about 2%, from about 1.25% to about 1.75%, or about 1.5%, by weight of said composition.
[0035] In certain embodiments, disclosed herein is an insecticide composition comprising flonicamid in an amount of from about 15% to about 30% by weight; a solvent system comprising DMSO in an amount of about from 17% to about 27% by weight, and pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo-methyl ester or a commercially available product comprising (or consisting essentially of) it (e.g., Rhodiasolv® PolarClean), in an amount of from about 25% to about 40% by weight; isotridecanol polyglycol ether 8 ethylene oxide or a commercially available product comprising it (e.g., Lutensol® TO 8), as an adjuvant, in an amount of from about 15% to about 30% by weight; and a mixture of alkenes, C11-C12, hydroformylation products, low boiling or a commercially available product comprising it such as Geronol AF 80, as an anti-foaming agent, in an amount of from about 0.5% to about 3% by weight. In particular such embodiments, the insecticide composition disclosed herein comprises flonicamid in an amount of from about 20% to about 27% by weight; DMSO in an amount of about from 20% to about 24% by weight; pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo-methyl ester or a commercially available product comprising (or consisting essentially of) it (e.g., Rhodiasolv® PolarClean), in an amount of from about 30% to about 35% by weight; isotridecanol polyglycol ether 8 ethylene oxide or a commercially available product comprising it (e.g., Lutensol® TO 8), in an amount of from about 20% to about 27% by weight; and a mixture of alkenes, C11-C12, hydroformylation products, low boiling or a commercially available product comprising it such as Geronol AF 80, in an amount of from about 1.25% to about 1.75% by weight. More particular such compositions are those comprising flonicamid in an amount of about 22.5% by weight; DMSO in an amount of about 21.5% by weight; pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo-methyl ester or a commercially available product comprising (or consisting essentially of) it (e.g., Rhodiasolv® PolarClean), in an amount of about 32% by weight; isotridecanol polyglycol ether 8 ethylene oxide or a commercially available product comprising it (e.g., Lutensol® TO 8), in an amount of about 22.5% by weight; and a mixture of alkenes, C11-C12, hydroformylation products, low boiling or a commercially available product comprising it such as Geronol AF 80, in an amount of about 1.5% by weight.
[0036] In other aspects, the present invention relates to methods for using an insecticide composition as defined in any one of the embodiments above, i.e., SL formulations containing high concentrations of flonicamid.
[0037] In one particular such aspect, disclosed herein is a method of controlling pest comprising applying to a locus where control of said pest is desired an effective amount of an insecticide composition as defined in any one of the embodiments above. In certain embodiments, the pest controlled by this method is an insect such as an aphid, a mealybug, and a white fly.
[0038] In another particular such aspect, disclosed herein is a method for the protection of a plant propagation material from an attack by a pest such as an insect, comprising treating the propagation material or the site where the propagation material is to be planted with an effective amount of a composition as defined herein.
[0039] The term “locus” as used herein refers not only to areas where the pest such as an insect may already be developed, but also to areas that have not yet been attacked by said pest, and to areas under cultivation. Locus includes the crop and propagation material of the crop (all the generative parts of the crop such as seeds and vegetative plant material such as cuttings and tubers, which can be used for the multiplication of the plant). Examples of propagation material of the crop include seeds, tubers, spores, corms, bulbs, rhizomes, sprouts basal shoots, stolons, buds and other parts of plants, including seedlings and young plants, which could be transplanted after germination or after emergence from soil. Locus also includes the area surrounding the crop and the growing media of the crop, such as soil and crop field.
[0040] In certain embodiments, the locus treated by the method disclosed herein above is a field of crop. The term “crop” (or “plant”) as used herein refers to whole plants, plant organs (e.g., leaves, stems, twigs, roots, trunks, limbs, shoots, fruits, etc.), plant cells, or plant seeds. Non-limiting examples of crops are oilseed rape (OSR), cotton, rice, banana, potato, coffee, sugar cane, citrus, beans, sunflower, apple, corn, soybean, wheat, barley, oats, chickpeas, fruit trees, nut trees, lentils, and grain sorghum.
[0041] Unless otherwise indicated, all numbers expressing, e.g., amounts of components or ratios between components, used in this specification, are to be understood as being modified in all instances by the term "about". Accordingly, unless indicated to the contrary, the numerical parameters set forth in this specification are approximations that
may vary by up to plus or minus 10% depending upon the desired properties to be obtained by the present invention.
[0042] The invention will now be illustrated by the following non-limiting Examples.
EXAMPLES
Materials and Methods
[0043] Materials. Dimethyl sulfoxide (DMSO; >99% purity) was purchased from Hubei Xingfa Chemicals Group Co; N-butyl-2-pyrrolidone (NBP) was purchased from Clariant AG; Agnique® AMD 3L ( N,N-di methyl lactamide) was purchased from BASF; Armid® FMPC (consisting of 80.0% by weight N- formyl morpholine and 20.0% by weight propylene carbonate) was purchased from Nouryon; flonicamid was purchased from Jingbo Agrochemicals Technology Co., Ltd.; and Rhodiasolv® PolarClean was purchased from Rhodia Poliamida e Especialidades Ltd.
[0044] Preparation of flonicamid-based soluble liquid (SL) formulations. A solid flonicamid was added to a stirred mixture of the appropriate solvent system, and the stirring continued until complete dissolution of the solid occurred. Then, if desired, an appropriate adjuvant was added with continuous stirring followed by the addition of a defoamer. The obtained clear solution was then filtered through a 5-micron filter.
Example 1. Solubility of flonicamid in various solvents
[0045] The solubility of flonicamid in various solvents was tested and shown in Table 1.
Table 1
Example 2. The stability of flonicamid-based soluble liquid (SL) formulations comprising different solvent systems
[0046] The stability of flonicamid-based SL formulations comprising flonicamid in an amount of 22.3% and various solvent systems is shown in Table 2.
Table 2
N/A - not available.
Example 3. Preparation of a particular flonicamid-based SL formulation [0047] A flonicamid-based formulation comprising DMSO and Rhodiasolv® PolarClean as a solvent system; Lutensol® TO 8 as an adjuvant; and Geronol AF 80 as an antifoaming agent (see Table 3), was prepared as described in Materials and Methods.
Table 3
Example 4. The stability of flonicamid-based SL formulation with various adjuvants [0048] The stability of flonicamid-based SL formulations comprising flonicamid (22.3%), DMSO (21.4%), Rhodiasolv® PolarClean (34%), and different adjuvants (22.3%) was evaluated, and the results are summarized in Table 4. The cold stability was evaluated at -10°C and 0°C, and the “compatibility” parameter indicates whether the tested formulation is compatible, i.e., clear at room temperature for at least one week, or is noncompatible, i.e., hazy, turbid and/or contains precipitants.
Table 4
Example 5. Bio-efficacy trials of flonicamid-based SL formulations
[0049] In the first trial, the biological efficacies of various flonicamid-based SL formulations having different adjuvants (either adjuvants comprised within the
formulation, i.e., built-in adjuvants, or tank mix adjuvants), wherein the ratio between the flonicamid and the adjuvant is about 1:1 by weight have been compared to that of the commercially available flonicamid-based product Teppeki® (water dispersible granules (WG) containing 500g/kg flonicamid), when applied on detached leaves on aphids’ mortality.
[0050] Preparation of the tested flonicamid-based SL formulations comprising build- in adjuvants. The tested formulations comprising build-in adjuvants were prepared as described above and the content of the tested formulations is shown in Table 5. After preparation, the formulations were diluted with water to obtain samples wherein the final concentration of flonicamid was 5 and 25 ppm, respectively.
[0051] Preparation of the tested flonicamid-based SL formulations with tank mix adjuvants. The SL250 formulation depicted in Table 5 was diluted with water to obtain a diluted formulation comprising flonicamid in a concentration of 5 or 25 ppm. Then, an appropriate adjuvant, i.e., methyl soyate or SK Enspray 99 (Hanyu Energy), at the same concentration (i.e., 5 or 25 ppm) was added.
Table 5
[0052] Results. Fig. 1 shows the mortality of aphids following the different treatments at two application rates (5 and 25 ppm) performed on detached cucumber leaves. The SL250+Silwet L-77, SL250+Lutensol, and SL250+SK Enspray 99 (tank mix adjuvant) formulations showed about 70-90% of aphids mortality at a rate of 25 ppm and were more potent as compared to the commercial product tested at this rate. The other tested formulations showed an improved efficacy of about 50-70% of aphids mortality at a rate of 5 ppm as compared to the commercial product at this rate.
[0053] In the second trial, the biological efficacy of various flonicamid-based SL formulations having different ratios of Silwet® L-77 adjuvant on aphids’ mortality was tested.
[0054] Preparation of flonicamid-based SL formulations having different ratios of Silwet® L-77 adjuvant. The SL250 and SL250+Silwet L-77 formulations depicted in Table 5 were diluted with water and mixed in appropriate ratios to obtain formulations with 25 ppm flonicamid and various ratios of adjuvant, i.e., from 0 to 25 ppm.
[0055] Results. Fig. 2 shows that there is a threshold for efficacy improvement, i.e., the efficacy of the tested formulations containing various amounts of adjuvant was constant and significantly increased only when the ratio between the flonicamid and adjuvant was 1:1.
[0056] In the third trial, the biological efficacies of four flonicamid-based formulations containing four different build-in adjuvants, two flonicamid-based formulations containing two different tank mix adjuvants, and a flonicamid-based formulation without an adjuvant, have been compared to that of the commercially available flonicamid-based product Teppeki®, in a contact and sucking assay with adult silverleaf whitefly Bemisia tabaci. The content of the tested flonicamid-based formulations is depicted in Table 5.
[0057] Assay method. 20 adult whiteflies were used and 4-6 replicates per treatment were performed. Foliar dip prior to the introduction of the pest by “leaf on-clip” cages.
[0058] Formulation preparation. Formulations with and without build-in adjuvants and commercial standard were prepared with tap water only by mixing all the components of the formulation with magnetic stirrer until homogeneous solutions were obtained.
[0059] Preparation of formulations containing tank mix adjuvants. An appropriate adjuvant was added to water under stirring until a stable emulsion was obtained. Then, flonicamid was added to obtain a final concentration of 2000 ppm of flonicamid.
[0060] Tank mix ratios. Ratios of flonicamid to adjuvant of 1-3.6: 1 were used.
[0061] Assessment times. Mortality was determined 72 hours after the exposure of the whiteflies to the treated plants.
[0062] Results. Table 6 shows the effect of the commercial Teppeki®, containing only flonicamid, compared to that of each one of the formulations (the adult mortality was
determined 72h after treatment). As clearly shown, the effect of the flonicamid-based formulations was faster than the that of the commercial Teppeki®. Adding an adjuvant to flonicamid-based formulations significantly increased the effectiveness of the flonicamid. It seems that treatment number 3 was the most effective one; however, the other formulations were not statistically different from each other. As further shown, the effect of each one of the adjuvants alone did not differ significantly from the water control.
Table 6
Percentage mortality was corrected for control mortality with Abbott's formula. The effect of the formulations on B. tabaci adults was compared 72h after treatment. Treatments were subjected to one-way analysis of variance (ANOVA); Percentage data were transformed (angular transformation=Arcsine) before statistical analysis. Means followed by a common letter do not differ significantly at p >().() 5.
REFERENCES
Kodandaram M.H., Rai A.B., Haider J. Novel insecticides for management of insect pests in vegetable crops: A review. Veg. Sci, 2010, 37, 109-123
Morita M., Ueda T., Yoeda T., Koyanagi T., Haga T. Flonicamid, a novel insecticide with a rapid inhibitory effect on aphid feeding. Pest Manag Sci., 2007, 63 969- 973
Morita M., Yoneda T., Akiyoshi N. Research and development of a novel insecticide, flonicamid. Journal of Pesticide Science , 2014, 39, 179-180
Ren M., Niu J., Hu B., Wei Q, Zheng C., Tian X., Gao C., He B., Dong K., Su J. Block of Kir channels by flonicamid disrupts salivary and renal excretion of insect pests. Insect Biochemistry and Molecular Biology, 2018, 99, 17-26
Claims (22)
1. An insecticide composition comprising flonicamid in an amount of from about 15% to about 30% by weight; and a solvent system comprising dimethyl sulfoxide (DMSO) and an additional solvent selected from pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo- methyl ester, N-(C1-C8)alkyl pyrrolidone, an amide of the formula R-C(0)-N(CH3)2 wherein R is (Ci-Ci2)alkyl, and a mixture thereof.
2. The composition of claim 1, wherein said N-(C1-C8)alkyl pyrrolidone is N-( Ci- C8)alkyl-2-pyrrolidone; and/or R is substituted, preferably at position a to the amide group, with a group selected from -OH, -0-(Ci-C6)alkyl, -CN, and -NO2.
3. The composition of claim 2, wherein said additional solvent is pentanoic acid 5- (dimethylamino)-2-methyl-5-oxo-methyl ester; A- b u t y 1 - 2 - p y rro 1 i do n c (NBP); N,N- dimethyl lactamide; or a mixture thereof.
4. The composition of claim 3, wherein said additional solvent is pentanoic acid 5- (dimethylamino)-2-methyl-5-oxo-methyl ester.
5. The composition of any one of claims 1-4, wherein the ratio between the DMSO and the additional solvent in said solvent system is from about 2:1 to about 1:4, from about 1:1 to about 1:2, or from about 1:1.5 to about 1:1.75, respectively, by weight.
6. The composition of any one of claims 1-5, further comprising at least one adjuvant each independently selected from an alcohol ethoxylate such as a polyethylene glycol (Cn- Ci4)alkyl ether and polyethylene glycol octylphenyl ether, a sorbitan ester alkoxylate, an alkoxylated polyol ester such as an ester of (Cis)unsaturated fatty acid with a polyethylene glycol ether with trimethylolpropane (3:1), and a trisiloxane ethoxylate such as 3-(2- methoxyethoxy)propyl-methyl-bis(trimethylsilyloxy)silane.
7. The composition of claim 6, wherein said at least one adjuvant each independently is isotridecanol polyglycol ether 8 ethylene oxide, or a mixture of polyethylene glycol (C11- Ci4)alkyl ethers enriched therewith.
8. The composition of claim 7, wherein said adjuvant is isotridecanol polyglycol ether 8 ethylene oxide.
9. The composition of any one of claims 6-8, wherein the ratio between said flonicamid and said adjuvant is from about 1:0.5 to about 1:2, respectively, by weight.
10. The composition of any one of claims 6-9, wherein the solvent system comprises DMSO in an amount of from about 17% to about 27% by weight, and pentanoic acid 5- (dimethylamino)-2-methyl-5-oxo-methyl ester in an amount of from about 25% to about 40% by weight.
11. The composition of claim 10, wherein the solvent system comprises DMSO in an amount of from about 20% to about 24% by weight, and pentanoic acid 5- (dimethylamino)-2-methyl-5-oxo-methyl ester in an amount of from about 30% to about 35% by weight.
12. The composition of any one of claims 6-11, further comprising an anti-foaming agent.
13. The composition of claim 12, wherein said anti-foaming agent is a mixture of alkenes, C11-C12, hydroformylation products, low boiling; a mineral oil-based defoamer; a blend of wax, hydrophobic silica, and mineral oil; a silicon emulsion; a polydimethyl siloxane emulsion; a silicone-based compound; or a mixture thereof.
14. The composition of claim 12 or 13, wherein said anti-foaming agent constitutes from about 0.5% to about 3% by weight of said composition.
15. The composition of claim 14, comprising flonicamid in an amount of from about 15% to about 30% by weight; DMSO in an amount of about from 17% to about 27% by weight; pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo-methyl ester in an amount of from about 25% to about 40% by weight; isotridecanol polyglycol ether 8 ethylene oxide in an amount of from about 15% to about 30% by weight; and a mixture of alkenes, C11- C12, hydroformylation products, low boiling in an amount of from about 0.5% to about 3% by weight.
16. The composition of claim 15, comprising flonicamid in an amount of from about 20% to about 27% by weight; DMSO in an amount of about from 20% to about 24% by weight; pentanoic acid 5-(dimethylamino)-2-methyl-5-oxo-methyl ester in an amount of from about 30% to about 35% by weight; isotridecanol polyglycol ether 8 ethylene oxide
in an amount of from about 20% to about 27% by weight; and a mixture of alkenes, Cii- Ci2, hydroformylation products, low boiling in an amount of from about 1.25% to about 1.75% by weight.
17. The composition of claim 16, comprising flonicamid in an amount of about 22.5% by weight; DMSO in an amount of about 21.5% by weight; pentanoic acid 5- (dimethylamino)-2-methyl-5-oxo-methyl ester in an amount of about 32% by weight; isotridecanol polyglycol ether 8 ethylene oxide in an amount of about 22.5% by weight; and a mixture of alkenes, C11-C12, hydroformylation products, low boiling in an amount of about 1.5% by weight.
18. A method of controlling pest comprising applying to a locus where control of said pest is desired an effective amount of a composition according to any one of claims 1-17.
19. The method of claim 18, wherein said pest is an insect such as an aphid, a mealybug, or a white fly.
20. The method of claim 18 or 19, wherein said locus is a field of crop.
21. The method of claim 20, wherein said crop is selected from oilseed rape (OSR), cotton, rice, banana, potato, coffee, sugar cane, citrus, beans, sunflower, apple, com, soybean, wheat, barley, oats, chickpeas, fruit trees, nut trees, lentils, and grain sorghum.
22. A method for the protection of a plant propagation material from an attack by a pest such as an insect, comprising treating the propagation material or the site where the propagation material is to be planted with an effective amount of a composition according to any one of claims 1-17.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US202163181576P | 2021-04-29 | 2021-04-29 | |
| US63/181,576 | 2021-04-29 | ||
| PCT/IL2022/050428 WO2022229956A1 (en) | 2021-04-29 | 2022-04-27 | Soluble liquid compositions comprising flonicamid and uses thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2022266180A1 true AU2022266180A1 (en) | 2023-11-16 |
Family
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Family Applications (1)
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|---|---|---|---|
| AU2022266180A Pending AU2022266180A1 (en) | 2021-04-29 | 2022-04-27 | Soluble liquid compositions comprising flonicamid and uses thereof |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP4329490A1 (en) |
| AR (1) | AR125476A1 (en) |
| AU (1) | AU2022266180A1 (en) |
| BR (1) | BR112023022731A2 (en) |
| WO (1) | WO2022229956A1 (en) |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5611535B2 (en) * | 2008-04-17 | 2014-10-22 | 石原産業株式会社 | Pest control composition and pest control method |
| CN101692817A (en) * | 2009-07-21 | 2010-04-14 | 深圳诺普信农化股份有限公司 | Pesticide composition and application thereof |
| CN101700036A (en) * | 2009-08-01 | 2010-05-05 | 深圳诺普信农化股份有限公司 | Pesticide composition and application thereof |
| CN102349504B (en) * | 2011-09-13 | 2013-09-11 | 广西田园生化股份有限公司 | Flonicamid-containing ultralow volume liquid agent |
| CN108077265A (en) * | 2017-12-29 | 2018-05-29 | 上海生农生化制品股份有限公司 | A kind of difenolan derivative pesticide composition and its application in pest control |
| CN111838160A (en) * | 2020-09-04 | 2020-10-30 | 安徽省四达农药化工有限公司 | Preparation and application of insecticidal composition containing flonicamid and dinotefuran |
-
2022
- 2022-04-27 BR BR112023022731A patent/BR112023022731A2/en unknown
- 2022-04-27 EP EP22723816.9A patent/EP4329490A1/en active Pending
- 2022-04-27 WO PCT/IL2022/050428 patent/WO2022229956A1/en active Application Filing
- 2022-04-27 AU AU2022266180A patent/AU2022266180A1/en active Pending
- 2022-04-28 AR ARP220101112A patent/AR125476A1/en unknown
Also Published As
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|---|---|
| EP4329490A1 (en) | 2024-03-06 |
| BR112023022731A2 (en) | 2024-01-02 |
| AR125476A1 (en) | 2023-07-19 |
| WO2022229956A1 (en) | 2022-11-03 |
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