A synergistic compound composition containing amide insecticides and its application
By combining compound I-72 with amide insecticides within a specific proportion range, forming a synergistic compound composition, the report problem of no compound compositions seen in the prior art was solved, and a variety of insect pests were achieved Effective prevention and control of mites has significantly improved the prevention and insecticide spectrum.
Patent Information
- Application Number
- CN202211520771.4
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Filing Date
- 2022-11-29
- Publication Date
- 2025-02-11
- Estimated Expiration
- 2042-11-29
AI Technical Summary
There is no report on compound compositions of compound I-72 and amide insecticides in the prior art, and it is difficult to effectively prevent and control a variety of pests and mites.
Using a synergistic compound composition, the compound I-72 is used to be used to form an amide insecticide (such as chlorobenzamide, flubenzamide, etc.) within a specific ratio range (1:50 to 50:1) Combination is carried out to form a composition with synergistic effects.
The compound composition significantly improves the prevention effect, reduces the dose of medicine, expands the insecticide spectrum, and can effectively prevent and control pests and mites on a variety of crops, delaying the generation of pest resistance.
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Figure CN118104671B_ABST
Abstract
Description
Technical Field
[0001] The invention belongs to the field of pesticides and relates to a synergistic compound composition containing amide insecticides and application thereof. Background Art
[0002] The price of developing new pesticides is rising. In contrast, the development and research of high-efficiency, low-toxic, and low-residue compounding and mixing has low investment and short development cycle, which has attracted attention at home and abroad, and efforts have been increased in development and research. Reasonable compounding or mixing of chemical agents has the positive characteristics of expanding the control spectrum, improving the control effect, extending the application period, reducing the amount of medicine, reducing the damage caused by the medicine, reducing the residue, and delaying the occurrence and development of drug resistance.
[0003] Amide insecticides are mainly divided into three categories: phthalamide, o-formamidobenzamide and m-formamidobenzamide. The amide insecticides currently on the market mainly include flubendiamide, chlorantraniliprole, cyantraniliprole, tetrachlorantraniliprole, and cyclofenac. Amide insecticides mainly act on nicotinic acid receptors, such as chlorantraniliprole, flubendiamide, cyantraniliprole, and tetrachlorantraniliprole; but there are also compounds with other mechanisms of action, such as bromofenac. In recent years, the amide insecticide market has grown rapidly, with annual sales approaching US$2 billion.
[0004] Chinese invention patent CN112457288 discloses a piperic acid derivative and its application, wherein compound I-72 has contact and stomach poison activity and good conduction activity, and can be used to control a variety of Lepidoptera, Hemiptera, Thysanoptera, Coleoptera and other pests. The compound has the following structural formula:
[0005]
[0006] The combination of different insecticide components may produce some unexpected technical effects and is also an effective method for preventing and controlling resistant pests and mites. However, there is no report on the combination of compound I-72 and amide insecticides. Summary of the invention
[0007] The purpose of the present invention is to provide a synergistic compound composition containing amide insecticides and application thereof.
[0008] To achieve the above purpose, the technical solution adopted by the present invention is:
[0009] A synergistic compound composition containing an amide insecticide, the composition comprising two active components A and B, component A being selected from a compound of the following structure (i.e., compound I-72), and component B being selected from an amide insecticide; the weight ratio of the two active components of components A and B being 1:50 to 50:1; wherein the compound structure of component A is as follows:
[0010]
[0011] The component B is selected from B1 chlorantraniliprole, B2 flubendiamide, B3 cyantraniliprole, B4 cyantraniliprole, B5 tetraniliprole, B6 tetrachlorantraniliprole, B7 cyhalodiamide, B8 thiotraniliprole, B9 flursulamid, B10 oxazolidinone (fenoxacrim), B11 tolfenpyrad, B12 cyclaniliprole, B13 cyclaniliprole, B14 ryania, B15 broflanilide, B16 cyproflanilide, B17 triflumilide, B18 fluchlordiniliprole, B19 tetrachlorfenapyr, B20 flubendiamide, B21 cyananthramide, B22 dimpropyridaz.
[0012] Preferably, in the composition, component A is selected from the above-mentioned structural compounds; component B is selected from B1 chlorantraniliprole, B2 flubendiamide, B3 cyantraniliprole, B4 cyantraniliprole, B5 tetraniline, B6 tetrachlorantraniliprole, B7 cyhalodiamide, B8 thiotraniliprole, B9 flursulamide, d), B10 fenoxacrim, B11 tolfenpyrad, B12 cyclaniliprole, B13 cyclanilide, B14 ryania, B15 broflanilide, B16 cyproflanilide, B17 triflumizone, B18 fluchlordiniliprole, B19 tetrachlorfenapyr, B20 flubendiamide, B21 cyananthramide, B22 dimpropyridaz;
[0013] The weight ratio of the two active components, component A and component B, is 1:20 to 20:1.
[0014] Further preferably, in the composition, component A is selected from the above-mentioned structural compounds; component B is selected from B1 chlorantraniliprole, B2 flubendiamide, B3 cyantraniliprole, B5 tetraniliprole, B6 tetrachlorantraniliprole, and B11 tolfenpyrad;
[0015] The weight ratio of the two active components A and B is 1:10 to 10:1.
[0016] The application of the composition is used for preparing insecticide drugs for preventing and controlling pests on fruit trees, vegetables, ornamental plants, tea, cotton, cereal crops, shrubs, broad-leaved trees, evergreen trees or urban health pests.
[0017] The composition is used for preventing or controlling pests of Lepidoptera, Hemiptera, Homoptera, Coleoptera, Diptera, Thysanoptera, Acarina, and their larvae and eggs.
[0018] The synergistic compound composition of the present invention has a significant synergistic effect in preventing and controlling pests on fruit trees, vegetables, ornamental plants, tea, cotton, cereal crops, shrubs, broad-leaved trees, evergreen trees or urban health pests. Indoor biological activity test results show that mixing compound I-72 with amide insecticides can improve the prevention effect, reduce the dosage, and expand the insecticide spectrum. For example, when compound I-72 is mixed with chlorantraniliprole, flubendiamide, cyantraniliprole, tetranilineprole, tetrachlorantraniliprole, and tolfenpyrad in a ratio of 1:10 to 10:1, the activity against striped stem borer, diamondback moth, peach aphid, beet armyworm, corn borer, thrips, and yellow flea beetle can be greatly improved; through a large number of experiments, it is found that after compound I-72 is mixed with amide insecticides, there is a significant synergistic trend with the increase of the amount of the compound, which is conducive to the application of the compound in the field. Therefore, the two active component compositions of the present invention can be used for the preparation of insecticide drugs.
[0019] The synergistic compound composition of the present invention can be used to control pests, mites, underground pests or urban health pests on fruit trees, vegetables, ornamental plants, tea, cotton, cereal crops, shrubs, broad-leaved trees, evergreen trees, etc.; it can be particularly used to control piercing-sucking mouthpart pests and lepidopteran pests, such as planthoppers, whiteflies, aphids, thrips, leafhoppers, stink bugs, as well as striped stem borers, corn borers, diamondback moths, armyworms, leaf miners, cotton bollworms, beet armyworms, termites and other pests and urban health pests on a variety of crops.
[0020] In particular, the synergistic composite composition of the present invention is particularly useful for controlling Hemiptera pests, a non-exhaustive list of which includes, but is not limited to, Acrosternum hilare, green stink bug, Blissus leucopterus, chinch bug, Calocoris norvegicus, Cimex hemipterus, tropical bed bug, Cimex lectularius, bed bug, Dagbertus fasciatus, Dichelops furcatus, Dysdercus suturellus, cotton bug, Edessa meditabunda, Eurygaster maura, cereal bug, Euschistus neotropicalis heros), Euschistus servus, Brown stink bug, Helopeltis antonii, Helopeltis theivora, Tea horn stink bug, Lagynotomus spp., stink bugs, Leptocorisa oratorius, Leptocorisa varicornis, Lygus spp., Lygus, Lygus hesperus, Western grass stink bug, Maconellicoccus hirsutus, Neurocolpus longirostris, Nezara viridula, Southern green stink bug, Phytocoris spp., Lygus, California plant stink bug californicus), Phytocoris relativus, Piezodorus guildingi, Poecilocapsus lineatus, Four-lined stink bug, Psallus vaccinicola, Pseudacysta perseae, Scaptocoris castanea, and Triatoma spp., bloodsucking conenose bugs / kissing bugs.
[0021] In particular, the synergistic composite composition of the present invention is particularly useful for controlling homopteran pests (aphids, scale insects, whiteflies, planthoppers, leafhoppers), a non-exhaustive list of which includes, but is not limited to, pea aphids (Acrythosiphon pisum), pea aphids, Adelges spp., aphids, cabbage whitefly (Aleurodes proletella), cabbage whitefly, spiral whitefly (Aleurodicus disperses), soft hair whitefly (Aleurothrixus floccosus), cotton whitefly, Aluacaspis spp., Amrasca bigutella bigutella, Aphrophora spp., leafhoppers, Aonidiella aurantii, Aphis spp., aphids of Aphis spp., cotton aphids (Aphis gossypii), cotton aphids, apple aphids (Aphis pomi), apple aphid, Aulacorthum solani, foxglove aphid, Bemisia spp., whitefly, Bemisia argentifolii, Bemisia tabaci, sweet potato whitefly, Brachycolus noxius, Russian aphid, Brachycorynella asparagi, asparagus aphid, Brevennia rehi, Brevicoryne brassicae, cabbage aphid, Ceroplastes spp. scale insects, Ceroplastes rubens, red wax scale insects, Chionaspis spp. scale insects, Chrysomphalus spp.), scale insects of the genus Coccus, Dysaphis plantaginea, pink apple aphid, leafhoppers of the genus Empoasca, woolly apple aphids Eriosoma lanigerum, woolly apple aphids, Icerya purchasi, woolly scale insects, Idioscopus nitidulus, mango leafhoppers, Laodelphax striatellus, brown planthoppers, Lepidosaphes, Macrosiphum.), potato aphid (Macrosiphum euphorbiae), potato aphid, wheat aphid (Macrosiphum granarium), English wheat aphid, rose aphid (Macrosiphum rosae), rose aphid, aster leafhopper (Macrosteles quadrilineatus), aster leafhopper, raspberry foamhopper (Mahanarva frimbiolata), wheat aphid (Metopolophium dirhodum), rose wheat aphid, long-horned bug (Mictis longicornis), peach aphid (Myzus persicae), green peach aphid, leafhoppers of the genus Nephotettix (Nephotettix spp.), black-tailed leafhopper (Nephotettix cinctipes), green leafhopper, green leafhopper, rice brown planthopper (Nilaparvata lugens), brown planthopper, bran shield scale (Parlatoria pergandii), bran scale, black scale scale (Parlatoria ziziphi), ebony scale, corn planthopper (Peregrinus maidis), corn flower-winged planthopper, Philaenus spp.'s scale, grape phylloxera (Phylloxera vitifoliae), grape phylloxera, spruce scale (Physokermes piceae), spruce round scale, planococcus spp., mealybugs, mealybugs of Pseudococcus spp., pineapple mealybug (Pseudococcus brevipes), pineapple mealybug, pear round scale (Quadraspidiotus perniciosus), St. Joseph's scale, Rhapalosiphum spp.), corn leaf aphids (Rhapalosiphummaida), corn aphids, grain aphids (Rhapalosiphum padi), grain aphids, scale insects of the genus Saissetia spp., olive black helmet scale insects (Saissetia oleae), black scale insects, Schizaphis graminum, green aphids, wheat long-tube aphids (Sitobion avenae), English wheat aphids, white-backed rice hoppers (Sogatella furcifera), white-backed planthoppers, aphids of the genus Therioaphis spp., scale insects of the genus Toumeyella spp., aphids of the genus Toxoptera spp., whiteflies (Trialeurodes spp.), greenhouse whitefly (Trialeurodes vaporariorum), greenhouse whitefly, green hemp whitefly (Trialeurodes abutiloneus), winged whitefly, scale insects of the genus Unaspis spp., Unaspis yanonensis, arrowhead scale insects, and Zulia entreriana.
[0022] In particular, the synergistic combination composition of the present invention is particularly useful for controlling Thysanoptera pests (thrips), a non-exhaustive list of which includes, but is not limited to, Frankliniella fusca, Tobacco thrips, Frankliniella occidentalis, Western flower thrips, Frankliniella shultzei, Frankliniella williamsi, Corn thrips, Heliothrips haemorrhaidalis, Greenhouse thrips, Riphiphorothrips cruentatus, Scirtothrips spp., Scirtothrips citri, Citrus thrips, Scirtothrips dorsalis, Scirtothrips dorsalis, Taeniothrips rhopalantennalis, and Thrips spp.
[0023] In particular, the synergistic composite composition of the present invention is particularly useful for controlling coleopteran (beetle) pests, a non-exhaustive list of which includes, but is not limited to: Acanthoscelides spp., weevils, Acanthoscelides obtectus, soybean weevils, Agrilus planipennis, ash borers, Agriotes spp., wireworms, Anoplophora glabripennis, Asian longhorn beetles, Anthonomus spp., weevils, Anthonomus grandis, boll weevils, Aphidius spp., Apion spp., weevils, Apogonia spp., grubs, Ataenius spretulus, turfgrass black beetle, beet cryptic beetle (Atomaria linearis), small beet beetle, melon beetle species (Aulacophora spp.), beet weevil (Bothynoderes punctiventris), beet root weevil, bean weevil species (Bruchus spp.), pea weevil (Bruchus pisorum), pea weevil, Cacoesia species, four-striped bean weevil (Callosobruchusmaculatus), southern cowpea weevil, yellow-spotted dew beetle (Carpophilus hemipteras), dried fruit beetle, beet tortoise beetle (Cassida vittata), Cerosterna species, Cerotoma species, leaf beetle, bean leaf beetle (Cerotomatrifurcata), bean leaf beetle, tortoise beetle species (Ceutorhynchus spp.), cabbage weevil (Ceutorhynchus assimilis), cabbage heart weevil, citrus weevil (Ceutorhynchus napi), cabbage weevil, Chaetocnema spp., Colaspis spp.), soil beetles, Conoderus scalaris, Conoderus stigmosus, Conotrachelus nenuphar, plum cone weevil, Cotinus nitidis, green flower beetle, Crioceris asparagi, asparagus leaf beetle, Cryptolestes ferrugineus, rusty flat flour beetle, Cryptolestes pusillus, flat flour beetle, Turkish flat flour beetle (Cryptolestesturcicus), Turkish flour beetle, Ctenicera spp., Curculio spp., Cyclocephala spp., Cylindrocpturus adspersus, sunflower stem weevil, Deporaus marginatus), mango leaf cutter weevil, Dermesteslardarius, ham weevil, Dermestes maculates, hidden beetle, Diabrotica spp. chrysolemid, Epilachna varivestis, Mexican bean beetle, Faustinus cubae, pale bark weevil, aggressive weevil, Hypera spp., Hypera postica, clover weevil, Hyperdoes spp., Argentine stem weevil, Hypothenemus hampei, coffee berry beetle, Ips spp., engraver beetle, Lasioderma serricorne), tobacco beetle, potato beetle (Leptinotarsa decemlineata), Colorado potato beetle, Liogenys fuscus, Liogenys suturalis, Lissorhoptrus oryzophilus, rice water weevil, Lyctus spp., wood beetle, powder beetle, Maecolaspis joliveti, Megascelis spp., corn beetle (Melanotus communis), cauliflower beetle (Meligethes spp.), Meligethes aeneus, Flower beetles, Melolontha melolontha, Common European beetle, Oberea brevis, Oberea linearis, Oryctes rhinoceros, Date palm beetle, Oryzaephilus mercator, Market saw-toothed grain beetle, Oryzaephilus surinamensis, Saw-toothed grain beetle, Otiorhynchus spp., Oulema melanopus, Grain leaf beetle, Oulema oryzae, Pantomorus spp., Phyllophaga spp., May / June beetle, June beetle cuyabana), Phyllotreta spp., Phyllotretavittuta fabr., Yellow curvy flea beetle, Yellow straight flea beetle, Yellow narrow flea beetle, Yellow wide flea beetle, Leaf beetle, Phynchites spp., Popillia japonica, Japanese beetle, Prostephanus truncates, Rhizopertha dominica, Rhizopertha dominica, Rhizotrogus spp., European beetle, Rhynchophorus spp., Scolytus spp., Wood beetle), Shenophorus spp., Sitonalineatus, Pea leaf weevil, Sitophilus spp. spp.), cereal weevils, grain weevils (Sitophilusgranaries), grain worms, rice weevils (Sitophilus oryzae), rice weevils, small round skin beetles (Stegobiumpaniceum), stealing beetles, Tribolium spp., flour beetles, red flour beetles (Triboliumcastaneum), red flour beetles, mixed flour beetles (Triboliumconfusum), mixed flour beetles, spotted skin beetles (Trogodermavariabile), warehouse beetles and greedy carabids (Zabrustenebioides).
[0024] In particular, the synergistic combination composition of the present invention is particularly useful for controlling lepidopteran pests, a non-exhaustive list of which includes, but is not limited to: Pyralidae, such as Chilosuppressalis (Walker), Tryporyzaincertulas (Walker), Cnaphalocrocis medinalis Guenee, Hellullaundalis, Conogethes punctiferlis; Pieridae, such as Pieris rapae, Papilio xuthus, Pierisrapaecrucivora, Parnara guttata; Arctiidae, such as Hyphantria nymphae, cunea); Noctuidae, such as trichoplusiani, mamestra brassicae, spodoptera exigua, spodoptera litura, helicoverpaarmigera, Pseudaletia separate, Agrotis ipsilon; Tortricidae, such as adoxophyes orana fasciata, archipsfuscocureanus, homona magnanima; Plutellidae, such as plutella xylotella; Gelechiidae, such as pectinophoragossypiella, Pink bollworm, etc.
[0025] In particular, the synergistic composite composition of the present invention can be used to control pests such as two-spotted spider mites, cinnabar spider mites, citrus leafminers, citrus scale insects, fruit leafminers, fruit borers, soybean borers, golden moths, tea geometrids, tea caterpillars, tea green leafhoppers, pear psyllids, rice planthoppers, greenhouse whiteflies, American leafminers, yellow-striped flea beetles, striped stem borers, yellow stem borers, corn borers, bean pod borers, melon borers, rice water weevils, cotton bollworms, pink bollworms, fruit aphids, soybean aphids, vegetable aphids, wheat aphids, cotton aphids, diamondback moths, armyworms, cabbage worms, tobacco budworms, longhorn beetles, mosquitoes, flies, cockroaches, termites, and other pests or urban health pests.
[0026] The synergistic compound composition of the present invention can be applied at an effective dose to the pests / mites to be controlled and / or their habitats. Therefore, the synergistic compound composition of the present invention provides a method for controlling or preventing plant pests.
[0027] The active ingredients in the synergistic compound composition of the present invention can be applied to pests, plants and their habitats simultaneously (for example, as a preformulated mixture or tank mix) or in a suitable sequence.
[0028] Advantages of the present invention: The binary composition obtained by compounding compound I-72 and amide insecticide in a suitable ratio has a good synergistic effect, thereby improving the prevention effect, reducing the dosage, and expanding the insecticide spectrum. Specifically, 1. The compounded two active components A and B have different mechanisms of action and can delay the development of insecticide resistance. 2. The insecticide spectrum is expanded and can be used to prevent and control various pests on various crops such as fruit trees, vegetables, ornamental plants, tea, cotton, etc.; 3. The amount of pesticide used is reduced, the amount of pesticide residues on crops is reduced, and the friendliness to the environment is enhanced. 4. The two active components A and B are compounded within a suitable ratio range to improve the control effect on target pests such as the striped stem borer, diamondback moth, peach aphid, beet armyworm, corn borer, thrips, etc. DETAILED DESCRIPTION
[0029] The following examples are used to explain the present invention in detail, so as to facilitate further understanding of the present invention. The active component A is selected from compound I-72 (prepared according to the description in the patent document CN112457288, with a content of 97%); the active component B and other raw materials are all commercially available products, and each component is measured by weight percentage.
[0030] Example 1: Indoor combined toxicity test of compound I-72 and chlorantraniliprole against Chilo suppressalis
[0031] Test target: 3rd instar larvae of Chilo suppressalis (Walker).
[0032] Preparation of drug solution: According to different test needs, use an electronic analytical balance to accurately weigh the test samples, dissolve the original drug in acetone, and then use 0.1% Tween 80 water to dilute it into a series of drug solutions with a certain concentration gradient according to the designed experimental dosage.
[0033] Experimental method: First, select tender rice stems and immerse them in the prepared solution for 10 seconds in the order from low dose to high dose according to the experimental design. After natural drying, place them in a culture dish with a diameter of 9 cm and filter paper, and inoculate neatly arranged healthy test insects. Each treatment has 10 heads and each treatment is repeated 3 times. A blank control (CK) is also set up.
[0034] Place the processed test materials in the observation chamber, where the temperature, humidity, and light can be adjusted as needed. After 72 hours, investigate the number of dead and live insects, calculate the corrected mortality rate using the Abbott formula, and perform statistical analysis using DPS data processing software to obtain the toxicity regression equations, LC 50 values and 95% confidence limits for each tested single agent and each different ratio mixture. Then, use the Sun Y-p method to calculate the co-toxicity coefficient of each ratio and evaluate the mixing effect. The test results are shown in Table 1.
[0035] The co-toxicity coefficient (CTC value) of the mixture is calculated according to the following formula:
[0036]
[0037] Where: ATI - Measured toxicity index of the mixture; S - LC of the standard agent 50 ; M - LC of the mixture 50 .
[0038] TTI = TIA × PA + TIB × PB
[0039] Where: TTI - Theoretical toxicity index of the mixture; TIA - Toxicity index of agent A; PA - Percentage content of agent A in the mixture; TIB - Toxicity index of agent B; PB - Percentage content of agent B in the mixture.
[0040]
[0041] Where: CTC - Co-toxicity coefficient; ATI - Measured toxicity index of the mixture; TTI - Theoretical toxicity index of the mixture.
[0042] The co-toxicity coefficient (CTC) of the compound mixture: CTC ≥ 120 indicates synergistic effect; 120 < CTC < 120 indicates additive effect; CTC ≤ 120 indicates antagonistic effect.
[0043] Table 1 Results of indoor combined toxicity determination of the mixture of Compound I-72 and Chlorantraniliprole against Chilo suppressalis
[0044]
[0045] Example 2: Indoor combined toxicity determination test of the mixture of Compound I-72 and Tetraniliprole against Plutella xylostella
[0046] Test target: 2nd instar larvae of Plutella xylostella.
[0047] Preparation of the liquid medicine: According to different test requirements, accurately weigh the tested samples respectively using an electronic analytical balance. The technical materials are dissolved in acetone and then diluted with 0.1% Tween 80 water into a series of liquid medicines with a certain concentration gradient according to the test design dose.
[0048] Experimental method: First, select cabbage leaves, and immerse them in the prepared solution for 10 seconds in the order from low dose to high dose according to the experimental design. After natural drying, place them in a culture dish with a diameter of 9 cm and filter paper, and inoculate neatly packed healthy test insects. Each treatment has 10 heads, and each treatment is repeated 3 times. A blank control is also set up.
[0049] The treated test materials were placed in an observation room, where the temperature, humidity, and light intensity could be adjusted as needed. After 72 hours, the number of dead and live insects was investigated, and the corrected mortality rate was calculated using the Abbott formula. The DPS data processing software was used for statistical analysis to determine the toxicity regression equations, LC values, and the toxicity of each single agent and each different ratio of the mixture. 50 The co-toxicity coefficient of each ratio was calculated by Sun Yunpei's method to evaluate the mixing effect (same as Example 1). The test results are shown in Table 2.
[0050] Table 2 Results of indoor combined toxicity test of compound I-72 and tetrazobactam against Plutella xylostella
[0051]
[0052]
[0053] Example 3: Indoor combined toxicity test of compound I-72 and cyantraniliprole against green peach aphid
[0054] Test target: Green peach aphid [Myzus persicae (Sulzer)] nymphs, a susceptible strain reared indoors.
[0055] Preparation of drug solution: According to different test needs, use an electronic analytical balance to accurately weigh the test samples, dissolve the original drug in acetone, and then use 0.1% Tween 80 water to dilute it into a series of drug solutions with a certain concentration gradient according to the designed experimental dosage.
[0056] Test method: First, select cabbage leaves with neat and uniform peach aphids, with each leaf carrying about 30-40 insects. Then, spray evenly from low dose to high dose according to the test design, 1.5 mL per leaf, repeat each treatment 3 times, and set up a blank control.
[0057] The treated test materials were placed in an observation room, where the temperature, humidity, and light intensity could be adjusted as needed. After 48 hours, the number of dead and live insects was investigated, and the corrected mortality rate was calculated using the Abbott formula. The DPS data processing software was used for statistical analysis to determine the toxicity regression equations, LC values, and the toxicity of each single agent and each different ratio of the mixture. 50The value and 95% confidence limit were calculated, and then the co-toxicity coefficient of each ratio was calculated by Sun Yunpei (Sun yp) method to evaluate the mixing effect (same as Example 1). The test results are shown in Table 3.
[0058] Table 3 Results of indoor combined toxicity test of compound I-72 and cyantraniliprole against green peach aphid
[0059]
[0060] Example 4: Indoor combined toxicity test of compound I-72 and tetrachlorantraniliprole against Spodoptera exigua
[0061] Test target: 2nd instar larvae of beet armyworm (Spodoptera exigua Hübner).
[0062] Preparation of drug solution: According to different test needs, use an electronic analytical balance to accurately weigh the test samples, dissolve the original drug in acetone, and then use 0.1% Tween 80 water to dilute it into a series of drug solutions with a certain concentration gradient according to the designed experimental dosage.
[0063] Experimental method: First, select cabbage leaves, and immerse them in the prepared solution for 10 seconds in the order from low dose to high dose according to the experimental design. After natural drying, place them in a culture dish with a diameter of 9 cm and filter paper, and inoculate neatly packed healthy test insects. Each treatment has 10 heads, and each treatment is repeated 3 times. A blank control is also set up.
[0064] The treated test materials were placed in an observation room, where the temperature, humidity, and light intensity could be adjusted as needed. After 72 hours, the number of dead and live insects was investigated, and the corrected mortality rate was calculated using the Abbott formula. The DPS data processing software was used for statistical analysis to determine the toxicity regression equations, LC values, and the toxicity of each single agent and each different ratio of the mixture. 50 The value and 95% confidence limit were calculated, and then the co-toxicity coefficient of each ratio was calculated by Sun Yunpei (Sun yp) method to evaluate the mixing effect (same as Example 1). The test results are shown in Table 4.
[0065] Table 4 Results of indoor combined toxicity test of compound I-72 and tetrachlorantraniliprole against Spodoptera exigua
[0066]
[0067] Example 5: Indoor combined toxicity test of compound I-72 and flubendiamide against corn borer
[0068] Test target: 3rd instar larvae of corn borer (Ostrinia furnacnlis Guenee).
[0069] Preparation of drug solution: According to different test needs, use an electronic analytical balance to accurately weigh the test samples, dissolve the original drug in acetone, and then use 0.1% Tween 80 water to dilute it into a series of drug solutions with a certain concentration gradient according to the designed experimental dosage.
[0070] Experimental method: First, select tender corn stalks and immerse them in the prepared solution for 10 seconds in the order from low dose to high dose according to the experimental design. After natural drying, place them in a culture dish with a diameter of 9 cm and filter paper, and inoculate neatly packed healthy test insects. Each treatment has 10 heads and each treatment is repeated 3 times. A blank control is also set up.
[0071] The treated test materials were placed in an observation room, where the temperature, humidity, and light intensity could be adjusted as needed. After 72 hours, the number of dead and live insects was investigated, and the corrected mortality rate was calculated using the Abbott formula. The DPS data processing software was used for statistical analysis to determine the toxicity regression equations, LC values, and the toxicity of each single agent and each different ratio of the mixture. 50 The co-toxicity coefficient of each ratio was calculated by Sun Yunpei's method to evaluate the mixing effect (same as Example 1). The test results are shown in Table 5.
[0072] Table 5 Results of indoor combined toxicity test of compound I-72 and flubendiamide against corn borer
[0073]
[0074]
[0075] Example 6: Indoor combined toxicity test of compound I-72 and tolfenpyrad against Thrips
[0076] Test target: nymphs of Thrips flavus Schrank.
[0077] Preparation of drug solution: According to different test needs, use an electronic analytical balance to accurately weigh the test samples, dissolve the original drug in acetone, and then use 0.1% Tween 80 water to dilute it into a series of drug solutions with a certain concentration gradient according to the designed experimental dosage.
[0078] Experimental method: First, select eggplant seedlings infested with yellow thrips, count the base number, and spray evenly in order from low dose to high dose according to the experimental design, 2 mL per plant, 3 replicates per treatment, and set up a blank control.
[0079] The treated test materials were placed in an observation room, where the temperature, humidity, and light intensity could be adjusted as needed. After 48 hours, the number of dead and live insects was investigated, and the corrected mortality rate was calculated using the Abbott formula. The DPS data processing software was used for statistical analysis to determine the toxicity regression equations, LC values, and the toxicity of each single agent and each different ratio of the mixture. 50The value and 95% confidence limit were calculated, and then the co-toxicity coefficient of each ratio was calculated by Sun Yunpei (Sun yp) method to evaluate the mixing effect (same as Example 1). The test results are shown in Table 6.
[0080] Table 6 Results of indoor combined toxicity test of compound I72 and tolfenpyrad against Thrips
[0081]
[0082] Example 7: Indoor combined toxicity test of compound I-72 and cyantraniliprole against yellow striped flea beetle
[0083] Test target: Adult yellow-striped flea beetle (Phyllotreta vittuta Fabr.).
[0084] Preparation of drug solution: According to different test needs, use an electronic analytical balance to accurately weigh the test samples, dissolve the original drug in acetone, and then use 0.1% Tween 80 water to dilute it into a series of drug solutions with a certain concentration gradient according to the designed experimental dosage.
[0085] Experimental method: First, select neat and consistent potted cabbage seedlings, and then spray them evenly in order from low dose to high dose according to the experimental design. After drying in the shade, transfer the treated cabbage seedlings to the adult flea beetles and cover them with glass covers, about 30-40 heads per plant. Each treatment is repeated 3 times, and a blank control is set up.
[0086] The treated test materials were placed in an observation room, where the temperature, humidity, and light intensity could be adjusted as needed. After 72 hours, the number of dead and live insects was investigated, and the corrected mortality rate was calculated using the Abbott formula. The DPS data processing software was used for statistical analysis to determine the toxicity regression equations, LC values, and the toxicity of each single agent and each different ratio of the mixture. 50 The co-toxicity coefficient of each ratio was calculated by Sun Yunpei's method to evaluate the mixing effect (same as Example 1). The test results are shown in Table 7.
[0087] Table 7 Results of indoor combined toxicity test of compound I-72 and cyantraniliprole against yellow striped flea beetle
[0088]
[0089] The description of the above embodiments is only used to help understand the method of the present invention and its core idea. It should be pointed out that for those of ordinary skill in the art, without departing from the principle of the present invention, the present invention can also be improved and modified in some ways, and these improvements and modifications also fall within the protection scope of the claims of the present invention. As can be seen from the above technical scheme, the synergistic composite composition of the present invention has the advantages of improving drug efficacy, expanding insecticide spectrum, reducing pesticide dosage, reducing the residual amount of pesticide on crops, alleviating pollution to the environment, being safe for humans and animals, having good environmental compatibility, and pests being difficult to develop drug resistance. The composition of the present invention can be applied to the prevention and treatment of various pests of various crops, and can be widely used in the field of agriculture.
Claims
1. A synergistic compound composition containing amide insecticides, characterized in that: The composition comprises two active components, A and B, wherein component A is selected from the compound of the following structure, and component B is selected from amide insecticides; the weight ratio of the two active components, A and B, is 1:50 to 50:1; wherein the compound structure of component A is as follows: ; The component B is selected from B1 chlorantraniliprole, B2 flubendiamide, B3 cyantraniliprole, B5 tetraniliprole, B6 tetrachlorantraniliprole, and B11 tolfenpyrad.
2. The composition according to claim 1, characterized in that: The weight ratio of the two active components, component A and component B, is 1:20 to 20:
1.
3. The composition according to claim 2, characterized in that: The weight ratio of the two active components A and B is 1:10 to 10:
1.
4. The use of the composition according to claim 1, characterized in that: The composition is used for preparing insecticides for preventing and controlling pests on fruit trees, vegetables, ornamental plants, tea, cotton, cereal crops, shrubs, broad-leaved trees and evergreen trees; the pests are one or more of Pyralidae, Plutella xylostellae, Myzus persicae, Noctuidae, Thrips fulvidraco and yellow-striped flea beetle.
5. The use of the composition according to claim 1, characterized in that: The composition is used for preventing or controlling Pyralidae, Plutella xylostellae, Myzus persicae, Noctuidae, Thrips fulvidraco, and yellow flea beetle pests and their larvae and eggs.
Citation Information
Patent Citations
Piperic acid derivative and application thereof
CN112457288A