Pesticide composition containing biphenyl sulfide compound and application thereof
By combining diphenyl sulfide compounds with other acaricides in a specific ratio, a pesticide composition is formed, which solves the problems of pest mite resistance and poor acaricidal effect, and achieves the effects of synergistic effect, cost reduction and extended duration.
Patent Information
- Application Number
- CN202411020442.2
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2024-07-29
- Publication Date
- 2025-09-05
- Estimated Expiration
- 2044-07-29
AI Technical Summary
In the prior art, chemical methods for controlling spider mites lead to drug resistance in the pest mites, and there is a lack of effective acaricide compositions to expand the acaricide spectrum, reduce the dosage and prolong the duration of the effect.
A pesticide composition is formed by combining biphenyl sulfide compounds with other acaricides in a specific ratio, including active ingredient A and active ingredient B. Through reasonable mixing, the acaricide spectrum is expanded, the cost of use is reduced, and the development of drug resistance is delayed.
Within a certain proportion range, the pesticide composition exhibits a synergistic effect, improves the acaricidal effect, reduces the cost of use, prolongs the effective period, reduces the amount of medicine used, and avoids the problem of cross-resistance.
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Abstract
Description
Technical Field
[0001] The present invention belongs to the field of pesticides, and in particular relates to a pesticide composition containing a diphenyl sulfide compound and application thereof. Background Art
[0002] Phytophagous mites are significant pests of many agricultural crops worldwide. If not controlled below economic thresholds, they threaten food, feed, and fiber production. In particular, species of mites from the Tetranychidae, Tenebrionidae, Tarsonematidae, and Mycobacteridae families are significant pests, directly feeding on plants or transmitting plant pathogens and viruses, harming crops.
[0003] Spider mites are a major agricultural pest, encompassing over 100 species. Their small size makes them difficult to identify. Coupled with global change, pesticide resistance, and cropping systems, spider mite damage is becoming increasingly severe. Common hosts for these pests include a variety of economic crops, including the Gramineae (corn), Malvaceae (cotton, hollyhock), Leguminosae (soybean, mung bean, red bean, common bean), Solanaceae (potato, eggplant, tomato, pepper), and Cucurbitaceae (cucumber, pumpkin, tomato, watermelon, winter melon). We found that the most common species of spider mites are Tetranychus truncatus, followed by Tetranychus pueraricola, Tetranychus kanzawai, and the red and green forms of Tetranychus urticae. These important agricultural pests are particularly susceptible to developing pesticide resistance due to their short reproductive cycles, high reproductive output, low mobility, and high self-fertilization.
[0004] For a long time, chemical control has been the primary method for controlling spider mites in production. The widespread use of chemical insecticides has made spider mites one of the most resistant pests. Reasonable chemical compounding or mixing has the positive advantages of expanding the insecticide spectrum, improving control effectiveness, extending the optimal application period, reducing dosage, minimizing pesticide damage, reducing residues, and delaying the development of pesticide resistance in pests. Summary of the Invention
[0005] To address the aforementioned problems in the prior art, the present invention provides a pesticide composition containing a diphenyl sulfide compound and its use. This pesticide composition effectively controls a variety of plant-feeding mites, exhibiting synergistic effects within a certain ratio range. It can broaden the spectrum of mites, reduce costs, minimize dosage, extend the duration of efficacy, and slow the development of resistance.
[0006] A pesticide composition containing a diphenyl sulfide compound, comprising an active ingredient A and an active ingredient B, wherein the active ingredient A is a diphenyl sulfide compound as shown in formula (I):
[0007] Active ingredient B is selected from one or more of the following acaricides
[0008] Insecticides and acaricides: B1 heterocyclics, B2 tetronic acids, B3 benzoyl acetonitrile, B4 oxazoles, B5 pyrazole amides, B6 biphenylhydrazines, B7 antibiotics, B8 organotin, B9 tetrazines, B 10 Thiazolidinones, B 11 Sulfites, B 12 Thiourea, B 13 Sulfoxides, B 14 Bridged cyclic amines, B 15 Quinolines, B 16 Quinazolines, B 17 Pyridazinones, B 18 Benzoylureas, B 19 Strobilurins, B 20 Parabens, B 21 Pyrazoles, B 22 Pyrroles, B 23 Pyrimidines, B 24 Naphthoquinones, B 25 Pyridazines, B 26 Pyrethroids, B 27 Biogenic, B 28 Non-systemic organic nitrogen, B 29 Other categories;
[0009] Furthermore, the active ingredient B is selected from:
[0010] B1 heterocyclics: pyridabenz, fenpyroximate;
[0011] B2 Tetraketamate: spirotetramat, spirodiclofen, spiromesifen, spirodiclofen, tetramesifen, tetramesifen;
[0012] B3 benzoylacetonitrile: cyfluthrin;
[0013] B4 oxazoles: etoxazole, fluxametamide, isocycloseram;
[0014] B5 Pyrazole amides: tebufenpyrad, tolfenpyrad, pyflubumide, ethoxifen, cypermethrin;
[0015] B6 Bifenazine: Bifenazate;
[0016] B7 antibiotics: avermectin, avermectin benzoate, liuyangmycin, huaguangmycin, and mibemycin;
[0017] B8 Organotin: triazotin, phenylbutatin;
[0018] B9 Tetrazines: clofentezine, fluazifop;
[0019] B 10 Thiazolidinones: hexathiazolin;
[0020] B 11 Sulfites: propargyl;
[0021] B 12 Thioureas: diafenthiuron, fenthiocarb;
[0022] B 13 Sulfoxides: flupentiofenox;
[0023] B 14 Bridged cyclic amines: acynonapyr;
[0024] B 15 Quinolines: flometoquin;
[0025] B 16 Quinazolines: quinazaquin;
[0026] B 17 Pyridazinones: pyridabenzin;
[0027] B 18 Benzoylureas: lufenuron, flufenoxuron, flufenoxuron, bistrifluan;
[0028] B 19 Strobilurins: pyrimidifen, fluazifop-butyl, pyrimidifen;
[0029] B 20 Benzoate esters: amidoflumet;
[0030] B 21 Pyrazoles: acetoprole, vaniliprole, fipronil;
[0031] B 22 Pyrroles: chlorfenapyr, chlorfenapyr;
[0032] B 23 Pyrimidines: pyrimidine ether;
[0033] B 24 Naphthoquinones: acarbaquinone;
[0034] B 25 Pyridazines: pyridabenzone;
[0035] B 26 Pyrethroids: highly effective flucythrin, deltamethrin, cypermethrin, bifenthrin, flumethrin, bromofluthrin;
[0036] B 27Biosources: matrine, veratridine, azadirachtin, pyrethrin, rotenone, pine mite shark, olive shark;
[0037] B 28 Non-systemic organic nitrogen: amitraz, monomitraz;
[0038] B 29 Other categories: at least one of mivorilaner, modoflaner, tigolaner, umifoxolaner, trifluoxetine, fluazinam, spinetoram, and mineral oil-based insecticides and acaricides.
[0039] Furthermore, the active ingredient B is selected from:
[0040] B1 heterocyclic: fenpyraclostrobin;
[0041] B2 quaternary acids: spirotetramat, spiromesifen;
[0042] B3 benzoylacetonitrile: cyfluthrin;
[0043] B4 oxazoles: etoxazole;
[0044] B5 Pyrazole amides: tolfenpyrad, ethoxyfenapyr, and pyraclostrobin;
[0045] B6 Bifenazine: Bifenazate;
[0046] B7 antibiotics: avermectin, avermectin benzoate;
[0047] B8 Organotin: triazotin;
[0048] B9 Tetrazines: clofentazine;
[0049] B 10 Thiazolidinones: hexathiazolin;
[0050] B 11 Sulfites: propargyl;
[0051] B 12 Thioureas: diafenthiuron;
[0052] B 18 Benzoylureas: lufenuron, bistrifluan;
[0053] B 19 Strobilurins: flutolane;
[0054] B 21 Pyrazoles: acetoprolin;
[0055] B 26 Pyrethroids: highly effective cyfluthrin, bifenthrin;
[0056] B 29 Others: at least one of trifluoxetine, spinetoram, and fluazinam insecticides and acaricides.
[0057] In the pesticide composition of the present invention, the mass ratio of the active ingredient A to the active ingredient B is not particularly limited, but is preferably 1:100 to 100:1 or any value between the above values;
[0058] Preferably, the mass ratio of the active ingredient A to the active ingredient B is 1:80 to 80:1;
[0059] More preferably, the mass ratio of the active ingredient A to the active ingredient B is 1:50 to 50:1;
[0060] More preferably, the mass ratio of the active ingredient A to the active ingredient B is 1:45 to 45:1.
[0061] In a specific embodiment, the present invention also lists the following specific combinations of active ingredient A and active ingredient B:
[0062]
[0063]
[0064] Furthermore, a specific combination of active ingredient A and active ingredient B:
[0065] Component A Component B Typical mass ratio Formula (I) Fenpyraclostrobin 25:1~1:24 Formula (I) Etoxazole 15:1~1:32 Formula (I) Abamectin 15:1~1:15 Formula (I) Methyl avermectin benzoate 50:1~5:1 Formula (I) clofentezine 15:1~1:27 Formula (I) Promethazine 20:1~1:20 Formula (I) diafenthiuron 18:1~1:18 Formula (I) Bistriflumuron 20:1~1:20 Formula (I) Trifluoxetine 15:1~1:20 Formula (I) Fluazinam 15:1~1:15
[0066] Furthermore, a specific combination of active ingredient A and active ingredient B:
[0067] Component A Component B Typical mass ratio Formula (I) Fenpyraclostrobin 25:1~1:14 Formula (I) Etoxazole 15:1~1:7 Formula (I) clofentezine 15:1~1:20 Formula (I) Abamectin 15:1~1:10 Formula (I) Methyl avermectin benzoate 50:1~5:1 Formula (I) Promethazine 14:1~1:20 Formula (I) diafenthiuron 18:1~1:18 Formula (I) Bistriflumuron 20:1~1:20 Formula (I) Trifluoxetine 15:1~1:20 Formula (I) Fluazinam 6:1~1:15
[0068] Furthermore, based on the total weight of the pesticide composition being 100 wt%, the sum of the content of the active ingredient A and the active ingredient B in the pesticide composition is 1 to 95 wt%;
[0069] Furthermore, the sum of the content of the active ingredient A and the active ingredient B in the pesticide composition is 1 to 90 wt%;
[0070] In a preferred embodiment, the sum of the content of the compound of formula (I) and pyrimethamine in the pesticide composition is
[0071]
[0072]
[0073] Furthermore, the sum of the contents of the compound of formula (I) and pyrimidifen in the pesticide composition is:
[0074]
[0075]
[0076] Furthermore, the pesticide composition further comprises, in addition to the active ingredient, auxiliary ingredients acceptable to agricultural production, wherein the auxiliary ingredients are selected from one or more of wetting agents, dispersants, emulsifiers, thickeners, disintegrants, antifreeze agents, defoaming agents, solvents, preservatives, stabilizers, synergists or carriers;
[0077] The wetting agent is selected from one or more of alkylbenzene sulfonate, alkylnaphthalene sulfonate, lignin sulfonate, sodium lauryl sulfate, sodium dioctyl sulfosuccinate, alpha olefin sulfonate, alkylphenol polyoxyethylene ether, castor oil polyoxyethylene ether, alkylphenol ethoxylate, fatty alcohol ethoxylate, fatty alcohol polyoxyethylene ether sodium sulfate, silkworm feces, soapberry powder, soapberry powder, SOPA, detergent, emulsifier 2000 series and wetting penetrant F; and / or
[0078] The dispersant is selected from one or more of lignin sulfonate, alkylnaphthalene sulfonate formaldehyde condensate, naphthalene sulfonate, tristyrylphenol ethoxylate phosphate, fatty alcohol ethoxylate, alkylphenol polyoxyethylene ether, alkylphenol polyoxyethylene ether methyl ether condensate sulfate, fatty amine polyoxyethylene ether, glycerol fatty acid ester polyoxyethylene ether, polycarboxylates, polyacrylic acids, phosphates, EO-PO block copolymers and EO-PO graft copolymers; and / or
[0079] The emulsifier is selected from one or more of calcium dodecylbenzenesulfonate, alkylphenol formaldehyde resin polyoxyethylene ether, phenylethylphenol polyoxyethylene polyoxypropylene ether, fatty alcohol ethylene oxide-propylene oxide copolymer, styrylphenol polyoxyethylene ether, castor oil polyoxyethylene ether and alkylphenol ether phosphate; and / or
[0080] The thickener is selected from one or more of xanthan gum, organobentonite, gum arabic, sodium alginate, magnesium aluminum silicate, carboxymethyl cellulose and white carbon black; and / or
[0081] Disintegrants: The disintegrants are selected from one or more of sodium sulfate, ammonium sulfate, aluminum chloride, sodium chloride, ammonium chloride, bentonite, glucose, sucrose, starch, cellulose, urea, sodium carbonate, sodium bicarbonate, citric acid and tartaric acid; and / or
[0082] The antifreeze agent is selected from one or more of alcohols, alcohol ethers, chlorinated hydrocarbons and inorganic salts; and / or
[0083] Defoaming agent selected from C 10 -C 20 Saturated fatty acid compounds, silicone oil, silicone compounds, C8-C 10One or more of fatty alcohols; and / or
[0084] The solvent is selected from one or more of benzene, toluene, xylene, durene, methanol, ethanol, isopropanol, n-butanol, dimethyl sulfoxide, dimethylformamide, cyclohexanone, alkylene carbonate, diesel, solvent oil, vegetable oil, vegetable oil derivatives and water; and / or
[0085] The preservative is selected from one or more of propionic acid, sodium propionic acid, sorbic acid, sodium sorbic acid, potassium sorbic acid, benzoic acid, sodium benzoic acid, sodium p-hydroxybenzoic acid, methyl p-hydroxybenzoate, kasone and 1,2-benzisothiazolin-3-one; and / or
[0086] The stabilizer is selected from one or more of disodium hydrogen phosphate, oxalic acid, succinic acid, adipic acid, borax, 2,6-di-tert-butyl-p-cresol, triethanolamine oleate, epoxidized vegetable oil, kaolin, bentonite, attapulgite, white carbon black, talc, montmorillonite and starch; and / or
[0087] Synergists are selected from synergist, piperonyl butoxide; and / or
[0088] The carrier is selected from one or more of ammonium salts, ground natural minerals, ground artificial minerals, silicates, resins, waxes, solid fertilizers, water, organic solvents, mineral oils, vegetable oils and vegetable oil derivatives;
[0089] The carrier is a solid carrier or a liquid carrier;
[0090] The solid carriers include: minerals, plants, synthetic fillers and inorganic salts;
[0091] The minerals include silicates, carbonates, sulfates and oxides.
[0092] The silicates are selected from at least one of kaolin, sepiolite, nacrite, montmorillonite, mica, vermiculite, pyrophyllite, and talc; the carbonates are selected from calcium carbonate or dolomite; the sulfates are selected from at least one of ammonium sulfate, sodium sulfate, and calcium sulfate; the oxides are selected from at least one of quicklime, magnesium lime, and diatomaceous earth; the plants are selected from at least one of citrus residue, corn cob cobs, husk powder, rice husk, soybean straw powder, tobacco powder, walnut shells, and sawdust powder; the synthetic fillers are selected from at least one of precipitated calcium carbonate hydrate, precipitated calcium carbonate, and white carbon black; and the inorganic salts are selected from potassium chloride or sodium chloride.
[0093] The liquid carrier includes water and an organic solvent;
[0094] The water is preferably deionized water;
[0095] The organic solvent is selected from at least one of aromatic hydrocarbons, chlorinated aliphatic hydrocarbons, aliphatic hydrocarbons, alcohols, ethers, ketones, special solvents, vegetable oils and methylated vegetable oils;
[0096] The aromatic hydrocarbon is selected from at least one of benzene, xylene, trimethylbenzene, and toluene; the chlorinated aliphatic hydrocarbon is selected from at least one of chloroform, dichloromethane, chloroform, carbon tetrachloride, and polychlorinated ethane; the aliphatic hydrocarbon is selected from at least one of petroleum fractions, cyclohexane, light mineral oil, and paraffin; the alcohol is selected from at least one of methanol, ethanol, isopropanol, butanol, isobutanol, ethylene glycol, propylene glycol, glycerol, and fatty alcohol; the ether is selected from at least one of propylene glycol ethyl ether, propylene glycol methyl ether, and petroleum ether; the ketone is selected from acetone, At least one of cyclohexanone, isophorone, N-methyl-pyrrolidone, and N-octylpyrrolidone; the special solvent is selected from at least one of dimethylformamide, dimethyl sulfoxide, polyethylene glycol, and capronitrile; the vegetable oil is selected from at least one of peanut oil, soybean oil, linseed oil, castor oil, and rapeseed oil; the methylated vegetable oil is selected from at least one of vegetable oleic acid methyl ester, animal oleic acid methyl ester, methyl laurate, methyl stearate, methyl myristate, methyl hexadecanoate, methyl caprylate, methyl caprylate, methyl coconut oleate, and mixed fatty acid methyl esters;
[0097] Furthermore, the pesticide composition can be prepared into an agriculturally acceptable formulation, wherein the formulation is selected from a solid formulation and / or a liquid formulation;
[0098] The solid preparations include powders, granules, pellets, tablets, strips, wettable powders, oil-dispersible powders, emulsion powders, water-dispersible granules, emulsion granules, water-dispersible tablets, soluble powders, soluble tablets or soluble granules;
[0099] The liquid preparations include soluble solutions, soluble gels, oils, film-spreading oils, emulsifiable concentrates, latexes, dispersible solutions, ointments, aqueous emulsions, oil emulsions, microemulsions, lipid suspensions, microcapsule suspensions, oil suspensions, dispersible oil suspensions, suspoemulsions, microcapsule suspension-suspension concentrates, microcapsule suspension-water emulsions, or microcapsule suspension-suspoemulsions;
[0100] Furthermore, the solid preparation is selected from wettable powder, water dispersible granules, soluble granules; the liquid preparation is selected from emulsifiable concentrate, water emulsion, suspension concentrate;
[0101] Use of a pesticide composition containing a diphenyl sulfide compound for controlling herbivorous mites;
[0102] The pest control method of the present invention allows for safer control of pests such as insects and mites with reduced dosages. The pest control composition of the present invention is suitable for use in pest control methods, particularly the pest control method of the present invention. The pest control composition of the present invention is particularly suitable for killing insects and mites in agricultural and horticultural applications.
[0103] Furthermore, the phytophagous pest mites are Tetranychus, Acaridae and / or Eupodidae pest mites;
[0104] Furthermore, the herbivorous pest mite is spider mite;
[0105] Furthermore, the spider mites are: Tetranychus truncatus, Tetranychus cinnabarinus, Panonychus citri, and Tetranychus urticae;
[0106] Furthermore, the acaricidal composition and / or its preparation is applied at an effective dose to the harmful mites to be controlled or the medium where they grow.
[0107] Beneficial effects of the present invention:
[0108] (1) The composition of the present invention exhibits a synergistic effect within the ratio range, and the acaricidal effect is significantly improved compared with a single agent, with good rapid effect and long-lasting effect;
[0109] (2) The active ingredients of the composition of the present invention do not have the problem of cross-resistance. By rationally mixing the different modes of action and different mechanisms of action of the pest mites, it can not only delay the development of pesticide resistance in the pest mites, but also reduce the amount of pesticide used;
[0110] (3) It is environmentally friendly, safe and efficient, and its promotion and application will have huge economic and social benefits. DETAILED DESCRIPTION
[0111] In order to make the technical solutions, objectives and advantages of the present invention more clearly understood, the present invention is described with reference to the following specific embodiments. However, the present invention can be implemented in various forms and should not be limited to the embodiments described herein.
[0112] Preparation example:
[0113] Preparation Example 1:
[0114] 26% formula (Ⅰ) compound·fenpyroximate suspension (22:4)
[0115] Preparation formula: 22% compound of formula (I), 4% fenpyroximate, 1% fatty alcohol polyoxyethylene ether, 3% phenethylphenol polyether phosphate, 1% sodium salt of polycarboxylate, 3% alkylaryl polyoxyethylene polyoxypropylene ether, 1% magnesium aluminum silicate, 0.25% xanthan gum, 0.1% kason, 5% ethylene glycol, 0.4% organosilicon defoamer, and deionized water to make up the balance;
[0116] Preparation method: According to the formula ratio of the embodiment, the active ingredients, surfactants and other functional additives are placed in a reactor in sequence, water is added and mixed evenly, and the suspension product is obtained by high-speed shearing, wet sand grinding, and finally homogenization filtration.
[0117] Preparation Example 2:
[0118] 20% formula (Ⅰ) compound·etoxazole suspension (10:10)
[0119] Preparation formula: 10% compound of formula (I), 10% etoxazole, 1% sodium dioctyl sulfonate succinate, 3% fatty alcohol polyoxyethylene ether phosphate, 1% naphthalenesulfonate formaldehyde condensate, 3% alkyl aryl polyoxyethylene polyoxypropylene ether, 1% magnesium aluminum silicate, 0.25% xanthan gum, 0.1% methylisothiazolinone, 5% glycerol, 0.4% organosilicon defoamer, and deionized water to make up the balance;
[0120] Preparation method: Same as Preparation Example 1.
[0121] Preparation Example 3:
[0122] 22% formula (I) compound·clofentezine suspension (4:18)
[0123] Preparation formula: 4% compound of formula (I), 18% clofentazine, 1.5% fatty amine polyoxyethylene ether, 3% phenylethylphenol polyether phosphate, 4% alkylaryl polyoxyethylene polyoxypropylene ether, 1% magnesium aluminum silicate, 0.25% xanthan gum, 0.1% kason, 5% propylene glycol, 0.4% silicone defoamer, and deionized water to make up the balance;
[0124] Preparation method: Same as Preparation Example 1.
[0125] Preparation Example 4:
[0126] 42% compound of formula (I)·difenthion suspension (22:20)
[0127] Preparation formula: 22% compound of formula (I), 20% diafenthiuron, 2% phenethylphenol polyether phosphate, 1% fatty amine polyoxyethylene ether, 1% polycarboxylic acid sodium salt, 1% alkylnaphthalene sulfonate formaldehyde condensate, 0.1% xanthan gum, 0.01% carboxyethyl cellulose, 1% sodium sorbate, 5% glycerol, 0.4% silicone defoamer, and deionized water to make up the balance;
[0128] Preparation method: Same as Preparation Example 1.
[0129] Preparation Example 5:
[0130] 34% Formula (I) compound·Fluazinam suspension (17:17)
[0131] Preparation formula: 17% compound of formula (I), 17% fluazinam, 2% alkyl naphthalene sulfonate formaldehyde condensate, 1% naphthalene sulfonate formaldehyde condensate, 3% styrenated phenol polyoxyethylene ether phosphate, 1% magnesium aluminum silicate, 0.16% xanthan gum, 5% propylene glycol, 0.02% potassium benzoate, 0.4% organosilicon defoamer, and deionized water to make up the balance;
[0132] Preparation method: Same as Preparation Example 1.
[0133] Preparation Example 6:
[0134] 5.5% formula (Ⅰ) compound·avermectin emulsifiable concentrate (5:0.5)
[0135] Preparation formula: 5% compound of formula (I), 0.5% avermectin, 12% styrylphenol polyoxyethylene ether, 3% calcium dodecylbenzenesulfonate, 10% N-methylpyrrolidone, 20% cyclohexanone, and xylene makes up the balance;
[0136] Preparation method: Add the active ingredients into a carrier according to the formula ratio of the embodiment, add a surfactant and other functional additives thereto, stir and mix them evenly in a stirring mixing kettle to obtain an emulsifiable concentrate product.
[0137] Preparation Example 7:
[0138] 15% compound of formula (I)·Promethazine microemulsion (1:14)
[0139] Preparation formula: 1% compound of formula (I), 14% propargyl methacrylate, 20% cyclohexanone, 15% styrylphenol polyoxyethylene ether, 3% alkylaryl polyoxyethylene polyoxypropylene ether, 1% fatty alcohol polyoxyethylene ether sulfate, 0.05% organosilicon defoamer, and deionized water to make up the balance;
[0140] Preparation method: According to the formula ratio of the embodiment, the active ingredients, solvent, emulsifier, etc. are mixed to prepare the oil phase, and the antifreeze agent and water are mixed to prepare the aqueous phase. The oil phase is added to the aqueous phase under stirring and stirred evenly. The shearing is continued for 10 minutes, and the defoaming agent is added and stirred evenly to obtain small droplets of oil phase particles with a size of 0.01 to 0.1 μm, thereby preparing the microemulsion product.
[0141] Preparation Example 8:
[0142] 12% compound of formula (I)·difenthuron microemulsion (10:2)
[0143] Preparation formula: 10% compound of formula (I), 2% diafenthiuron, 20% cyclohexanone, 15% styrylphenol polyoxyethylene ether, 3% sorbitan oleate polyoxyethylene ether, 1% fatty alcohol polyoxyethylene ether sulfate, 0.05% organosilicon defoamer, and deionized water to make up the balance;
[0144] Preparation method: Same as Preparation Example 7.
[0145] Preparation Example 9:
[0146] 13% formula (Ⅰ) compound·fenpyroximate aqueous emulsion (11:2)
[0147] Preparation formula: 11% compound of formula (I), 2% fenpyroximate, 20% cyclohexanone, 6% alkylaryl polyoxyethylene polyoxypropylene ether, and deionized water to make up the balance;
[0148] Preparation method: According to the formula ratio of the embodiment, the active ingredients are dissolved in the solvent and an emulsifier is added to dissolve it into a uniform oil phase. Deionized water and antifreeze are mixed together to form a uniform water phase; under high-speed shear, the water phase is added to the oil phase to form a water emulsion product.
[0149] Preparation Example 10:
[0150] 10% formula (Ⅰ) compound·clofentezine wettable powder (2:8)
[0151] Preparation formula: 2% compound of formula (I), 8% clofentazine, 2% fatty alcohol polyoxyethylene ether, 5% white carbon black, 8% formaldehyde condensate of sodium methylnaphthalene sulfonate, 10% tea saponin, 2% sodium lauryl sulfate, and kaolin to make up the balance;
[0152] Preparation method: According to the formula ratio of the embodiment, the active ingredients are added to the carrier, and the surfactant and other functional additives are added thereto, mixed, and then air flow pulverized and mixed again to obtain the wettable powder product.
[0153] Indoor toxicity
[0154] Examples Reference Pesticide Indoor Bioassay Test Guidelines Part 13: Leaf Disk Spray Method NY / T 1154.13-2008; Part 7: Determination of Combined Effects of Mixtures NY / T 1154.7-2006
[0155] Test agents: The technical of the compound of formula (I), fenpyraclostrobin technical, etoxazole technical, avermectin technical, avermectin benzoate technical, clofentezine technical, propargyl technical, diafenthiuron technical, bistrifluanyl technical, trifluanid technical, fluazinam technical, spirotetramat technical, etoxapyr technical, cypermethrin technical, bifenazate technical, hexathiazox technical, and lufenuron technical are all provided by the R&D center of the group;
[0156]
[0157]
[0158] Test target: citrus mite (panonychus citri McGregor);
[0159] Select female adult mites raised indoors with consistent physiological status. The temperature is (25±1)°C, the relative humidity is 65%±5%, and the photoperiod is 16 / 8h (L / D).
[0160] Select citrus leaves with uniform growth, use a hole puncher to make leaf discs with a diameter of 2 cm, place agar in a culture dish to keep it moist, place filter paper on it, and place leaf discs on the filter paper, with 3 leaf discs per dish, and inoculate adult mites raised indoors onto the leaf discs, with 10 to 15 mites on each leaf disc.
[0161] Preparation: Dissolve the original drug in acetone and dilute with a 0.1% Tween-80 solution. Prepare separate single-dose stock solutions. Design five groups of mixes based on the mixing objectives and drug activity. Prepare five series of mass concentrations for each single dose and each mix using the same ratio.
[0162] Chemical treatment: Place the petri dish on the bottom plate of a Potter spray tower and spray with a volume of 1 ml. Allow the solution to settle for 1 minute before removing it from the dish and transferring it to rearing conditions. Each treatment should be replicated at least four times, with at least 120 insects tested at each dose. A blank control containing no chemical (including all organic solvents and emulsifiers) should be used.
[0163] Data Statistics and Analysis: 48 hours after treatment, examine the insects for mortality and record the total insect count and the number of dead insects. Calculate the adjusted mortality rate for each treatment based on the survey data.
[0164] Calculate using the following formula, with the results rounded to two decimal places:
[0165]
[0166] Where:
[0167] P——mortality rate, in percentage (%);
[0168] K——indicates the number of dead insects, the unit is head;
[0169] N——represents the total number of insects processed, in heads.
[0170]
[0171] Where:
[0172] P1——adjusted mortality rate, in percentage (%);
[0173] P t ——Treatment mortality rate, expressed in percentage (%);
[0174] P0 - blank control mortality rate, in percentage (%).
[0175] If the control mortality rate is less than 5%, no correction is required; if the control mortality rate is between 5% and 20%, correction should be made; if the control mortality rate is greater than 20%, the test needs to be repeated.
[0176] The data were processed using the probability value analysis method. The LC of the toxicity regression line can be obtained by using the IBM SPSS Statistics 20 statistical analysis system. 50 The activity of the test agent on the biological test material was evaluated by using the b value and its 95% confidence limit.
[0177] The co-toxicity coefficient (CTC value) of the mixture is calculated as follows:
[0178]
[0179] Where:
[0180] ATI - measured toxicity index of mixture;
[0181] S——LC of standard acaricide 50 , the unit is milligrams per liter (mg / L);
[0182] M——LC of the mixture 50 , the unit is milligrams per liter (mg / L).
[0183] TTI=TI A *P A +TI B *P B
[0184] Where:
[0185] TTI – Theoretical Toxicity Index of Mixtures;
[0186] TI A ——Agent toxicity index;
[0187] P A ——The percentage of agent A in the mixture, in percentage (%);
[0188] TI B ——Toxicity index of agent B;
[0189] P B ——The percentage of agent B in the mixture, in percentage (%).
[0190]
[0191] Where:
[0192] CTC – Co-toxicity coefficient;
[0193] ATI - measured toxicity index of mixture;
[0194] TTI - Theoretical Toxicity Index of Mixture.
[0195] A co-toxicity coefficient (CTC) of 120 or higher indicates a synergistic effect; a co-toxicity coefficient (CTC) of 80 or lower indicates an antagonistic effect; and a co-toxicity coefficient (CTC) of 80 or lower indicates an additive effect.
[0196] Test results:
[0197] As can be seen from Table 1: The single dose of the compound of formula (I) showed a high toxicity to Panonychus citri, LC 50 The value was 11.279 mg / L. The indoor toxicity results of each single dose showed that the toxic effects of various acaricides on female adult mites of citrus mites were: fenpyroximate > avermectin > propargyl > diafenthiuron > fluazinam > etoxazole > clofentezine.
[0198] The compound of formula (I) exhibits a synergistic effect with fenpyroximate in the range of 25:1 to 1:24; the compound of formula (I) exhibits a synergistic effect with etoxazole in the range of 15:1 to 1:32; the compound of formula (I) exhibits a synergistic effect with clofentezine in the range of 15:1 to 1:20; the compound of formula (I) exhibits a synergistic effect with abamectin in the range of 15:1 to 1:15; the compound of formula (I) exhibits a synergistic effect with propargyl in the range of 20:1 to 1:20; the compound of formula (I) exhibits a synergistic effect with diafenthiuron in the range of 18:1 to 1:18; the compound of formula (I) exhibits a synergistic effect with fluazinam in the range of 15:1 to 1:15.
[0199] Table 1 Combined toxicity test of compound of formula (I) and various acaricides in different ratios against Panonychus citri (female adult mite)
[0200]
[0201]
[0202] The above test also tested the indoor toxicity of the compound of formula (I) mixed with emamectin benzoate, bistrifluan and triflumuron to Panonychus citri, and the results showed that:
[0203] When the active ingredient B is emamectin benzoate, its LC 50 It is 7.532 mg / L; when the mass ratio of the compound of formula (Ⅰ) to emamectin benzoate is 100:1~5:1, the co-toxicity coefficient is greater than 120, showing a synergistic effect. Among them, when the mass ratio of the compound of formula (Ⅰ) to emamectin benzoate is 16:1, the co-toxicity coefficient is the largest, which is 175.241, and the synergistic effect is most obvious.
[0204] When the active ingredient B is bistrifluan, its LC 50 It is 11.273 mg / L; when the mass ratio of the compound of formula (Ⅰ) to triflumuron is 20:1 to 1:20, the co-toxicity coefficient is greater than 120, showing a synergistic effect. Among them, when the mass ratio of the compound of formula (Ⅰ) to triflumuron is 3:4, the co-toxicity coefficient is the largest, which is 183.055, and the synergistic effect is most obvious.
[0205] When the active ingredient B is trifluoxetine, its LC 50 It is 15.251 mg / L; when the mass ratio of the compound of formula (Ⅰ) to trifluoxetine is 15:1 to 1:20, the co-toxicity coefficient is greater than 120, showing a synergistic effect. Among them, when the mass ratio of the compound of formula (Ⅰ) to trifluoxetine is 2:1, the co-toxicity coefficient is the largest, which is 217.108, and the synergistic effect is most obvious.
[0206] When the active ingredient B is spirotetramat, its LC 50 The total toxicity of the compound of formula (I) to spirotetramat was 272.433 mg / L; when the mass ratio of the compound of formula (I) to spirotetramat was 18:1 to 1:24, the co-toxicity coefficient was greater than 120, showing a synergistic effect. Among them, when the mass ratio of the compound of formula (I) to spirotetramat was 5:1, the co-toxicity coefficient was the largest, which was 207.529, and the synergistic effect was most obvious.
[0207] When the active ingredient B is ethoxyfenocitrile, its LC 50 It is 1.192 mg / L; when the mass ratio of the compound of formula (Ⅰ) to ethoxyfenocetyl is 35:1 to 1:25, the co-toxicity coefficient is greater than 120, showing a synergistic effect. Among them, when the mass ratio of the compound of formula (Ⅰ) to ethoxyfenocetyl is 5:1, the co-toxicity coefficient is the largest, which is 207.529, and the synergistic effect is most obvious.
[0208] When the active ingredient B is cypermethrin, its LC 50 It is 2.062 mg / L; when the mass ratio of the compound of formula (Ⅰ) to cypermethrin is 35:1 to 1:25, the co-toxicity coefficient is greater than 120, showing a synergistic effect. Among them, when the mass ratio of the compound of formula (Ⅰ) to cypermethrin is 2:3, the co-toxicity coefficient is the largest, which is 185.283, and the synergistic effect is most obvious.
[0209] When the active ingredient B is bifenazate, its LC 50 It is 3.1148 mg / L; when the mass ratio of the compound of formula (Ⅰ) to bifenazate is 35:1~1:30, the co-toxicity coefficient is greater than 120, showing a synergistic effect. Among them, when the mass ratio of the compound of formula (Ⅰ) to bifenazate is 2:7, the co-toxicity coefficient is the largest, which is 221.427, and the synergistic effect is most obvious.
[0210] When active ingredient B is hexythiazox, its LC 50 It is 12.072 mg / L; when the mass ratio of the compound of formula (Ⅰ) to hexythiazox is 30:1 to 1:25, the co-toxicity coefficient is greater than 120, showing a synergistic effect. Among them, when the mass ratio of the compound of formula (Ⅰ) to hexythiazox is 1:3, the co-toxicity coefficient is the largest, which is 193.057, and the synergistic effect is most obvious.
[0211] When the active ingredient B is lufenuron, its LC 50 It is 16.225 mg / L; when the mass ratio of the compound of formula (Ⅰ) to lufenuron is 35:1 to 1:25, the co-toxicity coefficient is greater than 120, showing a synergistic effect. Among them, when the mass ratio of the compound of formula (Ⅰ) to lufenuron is 5:2, the co-toxicity coefficient is the largest, which is 184.664, and the synergistic effect is most obvious.
[0212] Example 2
[0213] Field trials on Panonychus citri
[0214] Test crops: citrus trees (variety: Wenzhou mandarin orange);
[0215] Test subjects: Citrus spider mite (panonychus citri McGregor);
[0216] The test was conducted in Chuangxin Village, Huanxi Town, Jin'an District, Fuzhou City. The orchard was located on flat loamy soil with a pH of 6.0 and medium soil fertility (1g / kg organic matter content). The trees were uniformly grown and maintained with consistent fertilization and water management. The trees were eight years old, rootstocked with trifoliate oranges. The rows were spaced 5 x 4 meters apart, with 33 trees planted per mu. The average plant height was 2.0 meters, and the average canopy width was 2.0 x 2.5 meters. No fertilizer or irrigation was applied during the test.
[0217] Treatment: Each plot was randomly arranged in blocks, with 2 trees per plot and 4 replicates. The spraying equipment was a Singapore Linong 16-liter HD-400 backpack sprayer. The average spray volume per tree was 5.0 liters (4500 L / hm2). 2 ) Try to spray the medicine evenly and carefully, and wet the fruits, front and back of leaves and branches.
[0218] Test time: The pesticide was applied on April 28, 2021. Only one application was performed during the entire test process.
[0219] The weather was good on the day and during the test. On the day of the test, the average daily temperature was 18°C, the highest temperature was 23°C, the lowest temperature was 13°C, and the relative humidity was 70%.
[0220] Survey method: Two trees were surveyed in each plot, and 25 leaves of the spring shoots of the current year in different positions around the tree crown were randomly surveyed each time. A 10x insect magnifying glass was used to directly observe and record the number of live mites on the front and back of each leaf without removing the leaves in the field; the base number of mites was surveyed before spraying, and the number of live mites was surveyed 3 days and 14 days after spraying.
[0221] Calculation method of drug efficacy: The drug efficacy is calculated according to the following formula:
[0222]
[0223] During the experiment, the citrus trees in each treatment plot grew well and no phytotoxicity was observed in any treatment.
[0224] Test results:
[0225] Table 2 Test results of different test agents on citrus red spider mites
[0226]
[0227]
[0228] Note: The protective effect (%) in the above table is the average value of each replicate.
[0229] According to the field investigation, no adverse reactions to the pesticides were observed in leaves or twigs under any treatment, indicating that all treatments were safe for citrus growth at the concentrations used in the experiment.
[0230] Table 2 shows the field test results of different test agents against citrus spider mites. The compound of formula (I) mixed with fenpyroximate, abamectin, propargite, diafenthiuron, fluazinam, etoxazole, and clofentezine demonstrated excellent control efficacy against citrus spider mites, with efficacy significantly higher than that of the control agent alone. Three days after application, the control efficacy of each combination exceeded 90%, demonstrating good rapidity. Fourteen days after application, the control efficacy of each combination group increased, exceeding 90%, demonstrating good long-term efficacy.
[0231] Example 3
[0232] Field trials on orange spider
[0233] Test crops: Citrus (Lugan);
[0234] Test subjects: Citrus spider mite (panonychus citri McGregor);
[0235] The test was conducted in Shuangqiao Town, Wuming District, Nanning City, Guangxi Zhuang Autonomous Region. The orchard was located on flat loamy soil with a pH of 6.0. The soil fertility was moderate, the trees were uniform, and the fertilization and water management was consistent. The trees were six years old, with uniform age and canopy size across the field.
[0236] Treatment: Each plot was randomly arranged in blocks, with four trees per plot and four replicates. Pesticides were applied using a Singapore Linong 16-liter HD-400 backpack sprayer. Based on field conditions and farmer water usage habits, a water dosage of 1.5 liters per citrus tree was determined. Spraying was carried out evenly and thoroughly, wetting the fruit, front and back of leaves, and branches.
[0237] Test time: The pesticide was applied on October 18, 2022. Only one application was performed during the entire test process. The weather was good on the day and during the test.
[0238] Survey Method: Randomly select a point on each citrus plant in the east, west, south, north, and center directions. Mark a branch at each point and record the total number of live citrus red spider mites on the leaves of the marked branches (starting with the top leaf, with at least five leaves). Observe primarily adult and nymph mites (which can be observed with a magnifying glass). Count the base mite population before spraying, and the number of live mites 3 and 14 days after spraying.
[0239] Calculation method of drug efficacy: The drug efficacy is calculated according to the following formula:
[0240]
[0241] During the experiment, the citrus trees in each treatment plot grew well and no phytotoxicity was observed in any treatment.
[0242] Test results:
[0243] Table 3 Test results of different test agents on citrus red spider mites
[0244]
[0245] Note: The protective effect (%) in the above table is the average value of each replicate.
[0246] As shown in Table 3, field test results for different test agents against citrus spider mites indicate that the compound of formula (I) mixed with fenpyroximate, etoxazole, clofentezine, abamectin, propargyl, diafenthiuron, and fluazinam demonstrated excellent control efficacy against citrus spider mites, with efficacy significantly higher than that of the control single agent. Three days after application, the control efficacy of each combination exceeded 90%, demonstrating good rapidity. Fourteen days after application, the control efficacy of each combination group increased, exceeding 90%, demonstrating good long-term efficacy.
[0247] Indoor toxicity assays and field tests on citrus fruits have shown that acaricidal compositions formulated with the compound of formula (I) described herein and any of fenpyroximate, etoxazole, clofentezine, abamectin, propargyl, diafenthiuron, or fluazinam exhibit significant control efficacy against phytophagous mites. The resulting acaricidal compositions or formulations exhibit significant control efficacy, outperforming single agents in delaying the development of resistance and prolonging drug retention. Furthermore, no crop damage was observed with the combined formulations, demonstrating that the enhanced synergistic acaricidal efficacy of the resulting acaricidal compositions or formulations can reduce production and use costs, while maintaining crop safety.
[0248] Although the present invention has been described in detail above using general descriptions and specific implementation plans, it is obvious to those skilled in the art that some modifications or improvements can be made thereto based on the present invention. Therefore, these modifications or improvements made without departing from the spirit of the present invention shall fall within the scope of protection claimed by the present invention.
Claims
1. A pesticide composition containing a diphenyl sulfide compound, characterized in that: The pesticide composition comprises active ingredient A and active ingredient B, wherein active ingredient A is a diphenyl sulfide compound as shown in formula (I): Active ingredient B is selected from one or more insecticides and acaricides of the following acaricides: B1 heterocyclics, B2 tetronic acids, B3 benzoylacetonitrile, B4 oxazoles, B5 pyrazoleamides, B6 biphenylhydrazines, B7 antibiotics, B8 organotin, B9 tetrazines, B1 heterocyclics, B2 tetronic acids, B3 benzoylacetonitrile, B4 oxazoles, B5 pyrazoleamides, B6 biphenylhydrazines, B7 antibiotics, B8 organotin, B9 tetrazines, B1 heterocyclics, B1 ... heterocyclics, B1 heterocyclics, B1 10 Thiazolidinones, B 11 Sulfites, B 12 Thiourea, B 13 Sulfoxides, B 14 Bridged cyclic amines, B 15 Quinolines, B 16 Quinazolines, B 17 Pyridazinones, B 18 Benzoylureas, B 19 Strobilurins, B 20 Parabens, B 21 Pyrazoles, B 22 Pyrroles, B 23 Pyrimidines, B 24 Naphthoquinones, B 25 Pyridazines, B 26 Pyrethroids, B 27 Biogenic, B 28 Non-systemic organic nitrogen, B 29 Other categories.
2. The pesticide composition containing biphenyl sulfide compounds according to claim 1, characterized in that: The active ingredient B is selected from: B1 heterocyclics: pyridabenz, fenpyroximate; B2 Tetraketamate: spirotetramat, spirodiclofen, spiromesifen, spirodiclofen, tetramesifen, tetramesifen; B3 benzoylacetonitrile: cyfluthrin; B4 oxazoles: etoxazole, fluxametamide, isocycloseram; B5 Pyrazole amides: tebufenpyrad, tolfenpyrad, pyflubumide, ethoxifen, cypermethrin; B6 Bifenazine: Bifenazate; B7 antibiotics: avermectin, avermectin benzoate, liuyangmycin, huaguangmycin, and mibemycin; B8 Organotin: triazotin, phenylbutatin; B9 Tetrazines: clofentezine, fluazifop; B 10 Thiazolidinones: hexathiazolin; B 11 Sulfites: propargyl; B 12 Thioureas: diafenthiuron, fenthiocarb; B 13 Sulfoxides: flupentiofenox; B 14 Bridged cyclic amines: acynonapyr; B 15 Quinolines: flometoquin; B 16 Quinazolines: quinazaquin; B 17 Pyridazinones: pyridabenzin; B 18 Benzoylureas: lufenuron, flufenoxuron, flufenoxuron, bistrifluan; B 19 Strobilurins: pyrimidifen, fluazifop-butyl, pyrimidifen; B 20 Benzoate esters: amidoflumet; B 21 Pyrazoles: acetoprole, vaniliprole, fipronil; B 22 Pyrroles: chlorfenapyr, chlorfenapyr; B 23 Pyrimidines: pyrimidine ether; B 24 Naphthoquinones: acarbaquinone; B 25 Pyridazines: pyridabenzone; B 26 Pyrethroids: highly effective flucythrin, deltamethrin, cypermethrin, bifenthrin, flumethrin, bromofluthrin; B 27 Biosources: matrine, veratridine, azadirachtin, pyrethrin, rotenone, pine mite shark, olive shark; B 28 Non-systemic organic nitrogen: amitraz, monomitraz; B 29 Other categories: at least one of mivorilaner, modoflaner, tigolaner, umifoxolaner, trifluoxetine, fluazinam, spinetoram, and mineral oil-based insecticides and acaricides.
3. The pesticide composition containing biphenyl sulfide compounds according to claim 2, characterized in that: The active ingredient B is selected from: B1 heterocyclic: fenpyraclostrobin; B2 quaternary acids: spirotetramat, spiromesifen; B3 benzoylacetonitrile: cyfluthrin; B4 oxazoles: etoxazole; B5 Pyrazole amides: tolfenpyrad, ethoxyfenapyr, and pyraclostrobin; B6 Bifenazine: Bifenazate; B7 antibiotics: avermectin, avermectin benzoate; B8 Organotin: triazotin; B9 Tetrazines: clofentezine; B 10 Thiazolidinones: hexathiazolin; B 11 Sulfites: propargyl; B 12 Thioureas: diafenthiuron; B 18 Benzoylureas: lufenuron, bistrifluan; B 19 Strobilurins: flutolane; B 21 Pyrazoles: acetoprolin; B 26 Pyrethroids: highly effective cyfluthrin, bifenthrin; B 29 Others: at least one of trifluoxetine, spinetoram, and fluazinam insecticides and acaricides.
4. The pesticide composition containing a biphenyl sulfide compound according to claim 1, characterized in that: The mass ratio of the active ingredient A to the active ingredient B is 1:100 to 100:1; preferably 1:80 to 80:1; more preferably 1:50 to 50:1; further preferably 1:45 to 45:
1.
5. The pesticide composition containing biphenyl sulfide compounds according to claim 1, characterized in that: The mass ratio of the compound of formula (I) to fenpyroximate is 25:1 to 1:24; the mass ratio of the compound of formula (I) to etoxazole is 15:1 to 1:32; the mass ratio of the compound of formula (I) to clofentezine is 15:1 to 1:20; the mass ratio of the compound of formula (I) to abamectin is 15:1 to 1:15; the mass ratio of the compound of formula (I) to propargyl is 20:1 to 1:20; the mass ratio of the compound of formula (I) to diafenthiuron is 18:1 to 1:18; the mass ratio of the compound of formula (I) to fluazinam is 15:1 to 1:15; the mass ratio of the compound of formula (I) to emamectin benzoate is 100:1 to 5:1; the The mass ratio of the compound of formula (I) to bistrifluan is 20:1 to 1:20; the mass ratio of the compound of formula (I) to trifluanid is 15:1 to 1:20; the mass ratio of the compound of formula (I) to spirotetramat is 18:1 to 1:24; the mass ratio of the compound of formula (I) to ethidium bromide is 35:1 to 1:25; the mass ratio of the compound of formula (I) to cypermethrin is 35:1 to 1:25; the mass ratio of the compound of formula (I) to bifenazate is 35:1 to 1:30; the mass ratio of the compound of formula (I) to hexythiazox is 30:1 to 1:25; the mass ratio of the compound of formula (I) to lufenuron is 35:1 to 1:
25.
6. The pesticide composition containing biphenyl sulfide compounds according to claim 1, characterized in that: Based on the total weight of the pesticide composition being 100 wt%, the sum of the content of the active ingredient A and the active ingredient B in the pesticide composition is 1 to 95 wt%; Preferably, the total content of the active ingredient A and the active ingredient B in the pesticide composition is 5 to 80 wt%.
7. The pesticide composition containing a biphenyl sulfide compound according to claim 1, characterized in that: In addition to the active ingredients, the pesticide composition also includes auxiliary ingredients acceptable to agricultural biology, and the auxiliary ingredients are selected from one or more of wetting agents, dispersants, emulsifiers, thickeners, disintegrants, antifreeze agents, defoaming agents, solvents, preservatives, stabilizers, synergists or carriers.
8. The pesticide composition containing a biphenyl sulfide compound according to claim 5, characterized in that: The pesticide composition can be prepared into an agriculturally acceptable formulation, wherein the formulation is selected from a solid formulation and / or a liquid formulation; The solid preparations include powders, granules, pellets, tablets, strips, wettable powders, oil-dispersible powders, emulsion powders, water-dispersible granules, emulsion granules, water-dispersible tablets, soluble powders, soluble tablets or soluble granules; The liquid preparations include soluble solutions, soluble gels, oils, film-spreading oils, emulsifiable concentrates, latexes, dispersible solutions, ointments, aqueous emulsions, oil emulsions, microemulsions, lipid suspensions, microcapsule suspensions, oil suspensions, dispersible oil suspensions, suspoemulsions, microcapsule suspension-suspension concentrates, microcapsule suspension-water emulsions, or microcapsule suspension-suspoemulsions; Preferably, the solid preparation is selected from wettable powders, water-dispersible granules, and soluble granules; and the liquid preparation is selected from emulsifiable concentrates, aqueous emulsions, and suspensions.
9. Use of the pesticide composition containing a diphenyl sulfide compound according to any one of claims 1 to 8 for controlling phytophagous pest mites; Preferably, the phytophagous pest mites are Tetranychus, Acaridae and / or Eupodidae pest mites; More preferably, the phytophagous pest mite is spider mite.
10. The use according to claim 8, characterized in that The acaricidal composition and / or its preparation is applied at an effective dose to the harmful mites to be controlled or the medium where they grow.
Citation Information
Patent Citations
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Insecticidal and acaricidal composition
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CN114957062A
Synergistic acaricidal composition
CN117158429A
Application of diphenyl sulfide-containing compound for promoting yield increase and quality improvement of plants
CN117882716A
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