CN113016812B - Insecticidal and acaricidal synergistic composition and application thereof - Google Patents

Insecticidal and acaricidal synergistic composition and application thereof Download PDF

Info

Publication number
CN113016812B
CN113016812B CN201911345242.3A CN201911345242A CN113016812B CN 113016812 B CN113016812 B CN 113016812B CN 201911345242 A CN201911345242 A CN 201911345242A CN 113016812 B CN113016812 B CN 113016812B
Authority
CN
China
Prior art keywords
composition
insecticidal
test
mites
acaricidal
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201911345242.3A
Other languages
Chinese (zh)
Other versions
CN113016812A (en
Inventor
刘少武
宋玉泉
张俊龙
孙俊
班兰凤
于海波
李斌
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jiangsu Yangnong Chemical Co Ltd
Shenyang Sinochem Agrochemicals R&D Co Ltd
Original Assignee
Jiangsu Yangnong Chemical Co Ltd
Shenyang Sinochem Agrochemicals R&D Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Jiangsu Yangnong Chemical Co Ltd, Shenyang Sinochem Agrochemicals R&D Co Ltd filed Critical Jiangsu Yangnong Chemical Co Ltd
Priority to CN201911345242.3A priority Critical patent/CN113016812B/en
Publication of CN113016812A publication Critical patent/CN113016812A/en
Application granted granted Critical
Publication of CN113016812B publication Critical patent/CN113016812B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/581,2-Diazines; Hydrogenated 1,2-diazines
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/561,2-Diazoles; Hydrogenated 1,2-diazoles
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The invention belongs to the field of pesticides, and discloses an insecticidal and acaricidal composition containing A, B two active components and an application thereof, wherein the active component A is selected from pyrazotocillin; the active component B is selected from dimpropylidaz, acyclonapyr or isocycloseram. The weight part ratio of A, B two active components in the composition is 1: 50 to 50: 1. the composition has obvious synergistic effect, prolongs the control effect, reduces the pesticide consumption, and prevents pests and mites from generating drug resistance easily. The composition can be applied to the control of various pests and mites of various crops.

Description

Insecticidal and acaricidal synergistic composition and application thereof
Technical Field
The invention belongs to the field of pesticides, and particularly relates to an insecticidal and acaricidal synergistic composition containing pyrazoxyfen-ethyl and an application thereof.
Background
In the agricultural production process, the application of chemical agents is one of the most effective means for preventing and treating plant diseases and insect pests. The long-term continuous high-dose application of single chemical insecticide and acaricide easily causes the problems of medicament residue, environmental pollution, generation of drug resistance of pests and mites, and the like. The reasonable compounding or mixing of the chemical insecticide and the acaricide has the positive characteristics of expanding insecticidal and acaricidal spectrum, improving control effect, prolonging the application period, reducing the dosage, reducing phytotoxicity, reducing residues, delaying the occurrence and development of drug resistance and drug resistance of pests and mites, and the like.
Dimppyridaz is a formamidopyrazole insecticide developed by Pasteur, and is used for controlling piercing-sucking mouthpart pests; the acyclonapyr is a novel acaricide developed by Nippon Caoda corporation, has good control effect on pest mites of fruit trees, vegetables and tea trees, and is expected to be on the market in 2020; isocycloseram is an amide insecticide developed by prenatal corporation. The structural formulae of the three compounds are shown below:
Figure BDA0002333165510000011
disclosure of Invention
The invention aims to provide an insecticidal and acaricidal synergistic composition containing pyraclonil and application thereof.
In order to achieve the purpose, the invention adopts the technical scheme that:
an insecticidal and acaricidal synergistic composition containing chlorfenapyr and application thereof, the composition contains A, B two active components, the active component A is selected from chlorfenapyr; the active component B is selected from dimpropylidaz, acyclonapyr or isocycloseram; wherein the A, B weight part ratio of the two active components is 1: 50 to 50: 1.
Preferably: the component A in the composition is selected from the group consisting of pyrazotoconazole; component B is selected from dimipropyridaz; A. the weight part ratio of the two active components B is 1:20 to 20: 1.
the component A in the composition is selected from the group consisting of pyrazotoconazole; component B is selected from dimipropyridaz; A. the weight part ratio of the two active components B is 1: 10 to 10: 1.
the component A in the composition is selected from the group consisting of pyrazotoconazole; the component B is selected from acytonapyr; A. the weight part ratio of the two active components B is 1: 50 to 50: 1.
the component A in the composition is selected from the group consisting of pyrazotoconazole; component B is selected from isocycloseram; A. the weight part ratio of the two active components B is 1: 10 to 10: 1.
the cumulative weight content of active ingredients in the composition is 0.5% -95%.
The composition can be prepared into missible oil, suspending agent, water dispersible granule, aqueous emulsion, microemulsion, soluble liquid or wettable powder according to the needs.
The application of the composition and the application of the composition in preparing agricultural insecticide and acaricide medicaments. The insecticidal composition is used for preventing and controlling pests, mites or urban sanitary pests on fruit trees, vegetables, ornamental plants, tea, cotton and cereal crops.
According to the invention, a large number of tests prove the synergistic effect of the ethaboxam and different new compounds, and the indoor biological activity determination result shows that the combination of the ethaboxam and the dimpropylpridaz, acyclonapyr or isocyloseram in a proper proportion range can greatly improve the activity to tetranychus cinnabarinus and has higher activity to other target pests.
The insecticidal and acaricidal composition can be used for preventing and controlling pests, acarids or urban sanitary pests on fruit trees, vegetables, ornamental plants, tea, cotton and cereal crops; in particular, the insecticidal and acaricidal composition of the present invention is particularly useful for controlling harmful mites on panonychus citri, tetranychus citri, citrus mites, citrus leaf mites, tetranychus crataegi, panonychus ulmi, bryozoatum, tetranychus urticae, tetranychus theophyllus, tetranychus brachypomus, tetranychus telarius, tetranychus cinnabarinus, tetranychus truncatus, tetranychus turkestani, tetranychus dunhuang, red spider mites, tetranychus merdae, spider mites of the genus spider mites which are harmful to date trees, tetranychus mites of the genus prototetranychus, mites of vegetables, flowers and the like; can also be used for preventing and controlling aphids on fruit trees and vegetables such as cotton aphid, peach aphid, radish aphid, broad bean aphid, soybean aphid, meadowsweet aphid and the like; and whitefly or scale insect on fruits and vegetables, flowers and cotton, such as bemisia tabaci, whitefly, trialeurodes vaporariorum, Lecanicillium kummer, Lecanicillium peltatum, Lecanicillium kummer, etc.; and lepidoptera pests on fruit trees, vegetables and field crops such as chilo suppressalis, ostrinia nubilalis, cnaphalocrocis medinalis, sesamia inferens, plutella xylostella, spodoptera exigua, armyworm, prodenia litura, spodoptera frugiperda and the like. Therefore, the technical scheme of the invention also comprises the application of the acaricidal composition of the invention in preparing agricultural insecticidal and acaricidal agents.
The insecticidal and acaricidal composition can be applied to pests/mites and/or their habitat to be controlled in an effective dose.
The insecticidal and acaricidal composition has the following advantages: 1. the two compounded active components A, B have different action mechanisms, and can delay the generation of drug resistance of pests; 2. the using amount of the pesticide is reduced, the control effect is prolonged, the residual amount of the pesticide on crops is reduced, and the environmental friendliness is enhanced; 3. has special effect on various pests and mites on various crops.
The binary insecticidal and acaricidal composition containing the pyraclonil is used for improving the control effect, reducing the dosage and solving the problems of resistance generation, pesticide effect reduction and the like possibly caused by long-term use of single insecticidal and acaricidal agents.
Detailed Description
The following examples are presented to illustrate the invention in detail to facilitate a further understanding of the invention. The active ingredient A, B is prepared by conventional method, and the raw materials in the composition can be synthesized according to the prior art or obtained commercially; the composition can be prepared into corresponding dosage forms and can be automatically mixed according to the records of the prior art.
Example 1: indoor joint toxicity determination test of pyriproxyfen and dimpropylpyridazz mixed on tetranychus cinnabarinus
Test targets: tetranychus cinnabarinus (Boisdivaval) becomes a sensitive strain which is bred indoors.
Preparing a liquid medicine: according to different test requirements, accurately weighing the test samples by using an electronic analytical balance, dissolving the original medicine by using acetone, and diluting the dissolved original medicine into a series of liquid medicines with a certain concentration gradient by using 0.1% of Tween 80 water according to the test design.
The test method comprises the following steps: the activity of tetranychus cinnabarinus on tetranychus cinnabarinus is determined by a spraying method. Firstly, inoculating tetranychus cinnabarinus with consistent size to kidney bean seedling leaves in a first true leaf flattening period, and counting the base number after the tetranychus cinnabarinus is stabilized; then, the mixture was uniformly sprayed in the order of low concentration to high concentration according to the experimental design, 1.5mL of each plant was treated 3 times, and a blank control was additionally provided. And (3) placing the treated test material in an observation chamber, wherein the temperature, the humidity and the illumination of the observation chamber can be adjusted as required. The number of dead and live mites was investigated after 72 hours. Calculating corrected mortality by abbott formula, performing statistical analysis by DPS data processing software, and calculating toxicity regression equation and LC for each single agent and different mixture ratio50The values and the 95% confidence limits, the cotoxicity coefficient of each proportion is calculated by a Sun cloud Peel (Sun y-p) method, the mixed effect is evaluated, and the test results are shown in table 1.
The co-toxicity coefficient (CTC value) of the mixture was calculated according to the following formula:
Figure BDA0002333165510000033
in the formula: actually measuring a toxicity index of the ATI-mixed agent; LC of S-Standard drug50(ii) a LC of M-mixtures50
TTI=TIA×PA+TIB×PB
In the formula: TTI-mixture theory virulence index; TIA-A agent virulence index; the percentage content of the PA-A medicament in the mixture; TIB-B agent virulence index; the percentage content of the PB-B medicament in the mixture.
Figure BDA0002333165510000031
In the formula: CTC-co-toxicity coefficient; actually measuring a toxicity index of the ATI-mixed agent; TTI-mixture theory virulence index.
Co-toxicity coefficient (CTC) of the combination: CTC is more than or equal to 120 and shows synergistic effect; CTC is less than or equal to 80 and shows antagonism; 80< CTC <120 shows additive effects.
TABLE 1 results of indoor combined toxicity determination of Tetranychus cinnabarinus by compounding ethacrylonitrile and dimpropylpyridaz
Figure BDA0002333165510000032
Example 2: metronidazole and dimipropyridaz mixed pairing peach aphid indoor combined toxicity determination test
Test targets: the green peach aphid (Myzus persicae (Sulzer)) is a sensitive strain which is bred indoors if the green peach aphid is aphid.
Preparing a liquid medicine: according to different test requirements, accurately weighing the test samples by using an electronic analytical balance, dissolving the original medicine by using acetone, and diluting the dissolved original medicine into a series of liquid medicines with a certain concentration gradient by using 0.1% of Tween 80 water according to the test design.
The test method comprises the following steps: and (3) determining the activity of the green aphids and the green aphids of the peach aphids by adopting a spraying method. Firstly, cabbage seedling leaves with tidy and consistent green peach aphids are selected, the insect loading capacity of each leaf is about 40, then the cabbage seedling leaves are uniformly sprayed in the sequence from low concentration to high concentration according to the experimental design, each leaf is 1.5mL, each treatment is repeated for 3 times, and a blank control is additionally arranged. And (3) placing the treated test material in an observation chamber, wherein the temperature, the humidity and the illumination of the observation chamber can be adjusted as required. After 48 hours, the number of dead and live insects was investigated. Calculating corrected mortality by abbott formula, performing statistical analysis by DPS data processing software, and calculating toxicity regression equation and LC for each single agent and different mixture ratio50The values and 95% confidence limits, the cotoxicity coefficient of each proportion is calculated by a Sun cloud Peel (Sun y-p) method, the mixing effect is evaluated (the same as the example 1), and the test results are shown in a table 2.
TABLE 2 results of indoor combined toxicity assay of Amycolatopyr and dimipropyridaz for Myzus persicae
Figure BDA0002333165510000041
Example 3: indoor joint toxicity determination test of tetrazoxynil and acytonapyr mixed on tetranychus cinnabarinus
Test targets: tetranychus cinnabarinus (Boisdivaval) becomes a sensitive strain which is bred indoors.
Preparing a liquid medicine: according to different test requirements, accurately weighing the test samples by using an electronic analytical balance, dissolving the original medicine by using acetone, and diluting the dissolved original medicine into a series of liquid medicines with a certain concentration gradient by using 0.1% of Tween 80 water according to the test design.
The test method comprises the following steps: the activity of tetranychus cinnabarinus on tetranychus cinnabarinus is determined by a spraying method. Firstly, inoculating tetranychus cinnabarinus with consistent size to kidney bean seedling leaves in a first true leaf flattening period, and counting the base number after the tetranychus cinnabarinus is stabilized; then, the mixture was uniformly sprayed in the order of low concentration to high concentration according to the experimental design, 1.5mL of each plant was treated 3 times, and a blank control was additionally provided. And (3) placing the treated test material in an observation chamber, wherein the temperature, the humidity and the illumination of the observation chamber can be adjusted as required. The number of dead and live mites was investigated after 72 hours. Calculating corrected mortality by abbott formula, performing statistical analysis by DPS data processing software, and calculating toxicity regression equation and LC for each single agent and different mixture ratio50The values and 95% confidence limits, the cotoxicity coefficient of each proportion is calculated by a Sun cloud Peel (Sun y-p) method, the mixing effect is evaluated (the same as the example 1), and the test results are shown in a table 3.
TABLE 3 indoor combined toxicity test results of YZOMANNITRILE AND ACYONapyr
Figure BDA0002333165510000042
Figure BDA0002333165510000051
Example 4: indoor joint toxicity determination test of tetrazotocid nitrile and isocycloseram mixed on tetranychus cinnabarinus
Test targets: tetranychus cinnabarinus (Boisdivaval) becomes a sensitive strain which is bred indoors.
Preparing a liquid medicine: according to different test requirements, accurately weighing the test samples by using an electronic analytical balance, dissolving the original medicine by using acetone, and diluting the dissolved original medicine into a series of liquid medicines with a certain concentration gradient by using 0.1% of Tween 80 water according to the test design.
The test method comprises the following steps: the activity of tetranychus cinnabarinus on tetranychus cinnabarinus is determined by a spraying method. Firstly, inoculating tetranychus cinnabarinus with consistent size to kidney bean seedling leaves in a first true leaf flattening period, and counting the base number after the tetranychus cinnabarinus is stabilized; then, the mixture was uniformly sprayed in the order of low concentration to high concentration according to the experimental design, 1.5mL of each plant was treated 3 times, and a blank control was additionally provided. And (3) placing the treated test material in an observation chamber, wherein the temperature, the humidity and the illumination of the observation chamber can be adjusted as required. The number of dead and live mites was investigated after 72 hours. Calculating corrected mortality by abbott formula, performing statistical analysis by DPS data processing software, and calculating toxicity regression equation and LC for each single agent and different mixture ratio50The values and 95% confidence limits, the cotoxicity coefficient of each proportion is calculated by a Sun cloud Peel (Sun y-p) method, the mixing effect is evaluated (the same as the example 1), and the test results are shown in a table 4.
TABLE 4 indoor combined toxicity test results of the mixture of ethacrylonitrile and isocycloseram on Tetranychus cinnabarinus
Figure BDA0002333165510000052
Example 5: indoor combined toxicity determination test of pyriminostrobin and isocycloseram mixed on corn borer
Test targets: 3 rd larva of Ostrinia furnacalis (Ostrinia furnacalis), a sensitive strain raised indoors.
Preparing a liquid medicine: according to different test requirements, accurately weighing the test samples by using an electronic analytical balance, dissolving the original medicine by using acetone, and diluting the dissolved original medicine into a series of liquid medicines with a certain concentration gradient by using 0.1% of Tween 80 water according to the test design.
The test method comprises the following steps: the activity of the pesticide composition on the larvae of the corn borers is determined by a pharmacothraxis method. Firstly, selecting a standard clean 24-hole culture plate, adding 1mL of artificial feed into each hole, cooling and solidifying, adding 0.05mL of liquid medicine into each hole of the culture plate by using a continuous sampler, naturally drying in the shade, selecting neat and consistent test insects, inoculating the test insects into the culture plate, wherein 1 head of each hole is reserved every time of treatment, and repeating each treatment3 times, and a blank control is additionally arranged. And (3) placing the treated test material in an observation chamber, wherein the temperature, the humidity and the illumination of the observation chamber can be adjusted as required. The number of dead and live insects was investigated after 72 hours. Calculating corrected mortality by abbott formula, performing statistical analysis by DPS data processing software, and calculating toxicity regression equation and LC for each single agent and different mixture ratio50The values and 95% confidence limits, the co-toxicity coefficient of each ratio was calculated by Sun cloud Peel (Sun y-p) method, and the blending effect was evaluated (same as example 1), and the test results are shown in Table 5.
TABLE 5 results of indoor combined toxicity assay of Chlorobipyr B and Isocylseram
Figure BDA0002333165510000061
The results of the indoor bioactivity assay showed that metconazole and dimiprypyridaz were measured at a ratio of 1:20 to 20: 1, the composition can greatly improve the activity to tetranychus cinnabarinus, and the content of the pyrazotocin and the dipropyridaz is 1: 10 to 10:1, the activity to the green peach aphids can be greatly improved, and the content of the pyrazotoconazole and the acrynonapyr is 1: 50 to 50: 1, has better synergistic activity on tetranychus cinnabarinus, and in addition, the content of the chlorfenapyr and isocycloseram is 1: 10 to 10:1, the activity to tetranychus cinnabarinus and corn borer can be greatly improved.
The above description of the embodiments is only intended to facilitate the understanding of the method of the invention and its core idea. It should be noted that, for those skilled in the art, it is possible to make various improvements and modifications to the present invention without departing from the principle of the present invention, and those improvements and modifications also fall within the scope of the claims of the present invention. In conclusion, the composition has the advantages of obvious synergy, less environmental pollution, difficult generation of phytotoxicity, capability of delaying the generation of drug resistance of pests and wide application in the agricultural field.

Claims (4)

1. An insecticidal and acaricidal synergistic composition containing pyraclonil, which is characterized in that: the composition contains A, B two active components, wherein the active component A is selected from pyrazotoconazole; the active component B is selected from acytonapyr; wherein the A, B weight part ratio of the two active components is 1: 50 to 50: 1 and is not 1:20, 10: 1.
2. The composition according to claim i, characterized in that: the cumulative weight content of active ingredients in the composition is 0.5% -95%.
3. The composition according to claim l or 2, characterized in that: the composition is prepared into missible oil, a suspending agent, a water dispersible granule, an aqueous emulsion, a microemulsion, a soluble liquid or a wettable powder.
4. Use of a composition according to claim i, characterized in that: the composition is applied to the preparation of carmine spider mite killing drugs.
CN201911345242.3A 2019-12-24 2019-12-24 Insecticidal and acaricidal synergistic composition and application thereof Active CN113016812B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201911345242.3A CN113016812B (en) 2019-12-24 2019-12-24 Insecticidal and acaricidal synergistic composition and application thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201911345242.3A CN113016812B (en) 2019-12-24 2019-12-24 Insecticidal and acaricidal synergistic composition and application thereof

Publications (2)

Publication Number Publication Date
CN113016812A CN113016812A (en) 2021-06-25
CN113016812B true CN113016812B (en) 2022-02-11

Family

ID=76451480

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201911345242.3A Active CN113016812B (en) 2019-12-24 2019-12-24 Insecticidal and acaricidal synergistic composition and application thereof

Country Status (1)

Country Link
CN (1) CN113016812B (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106605654A (en) * 2015-10-21 2017-05-03 陕西韦尔奇作物保护有限公司 Insecticidal composition containing SYP-9625
CN109645002A (en) * 2018-12-13 2019-04-19 广东中迅农科股份有限公司 Synergetic pesticide composition containing D- limonene
CN109964948A (en) * 2019-05-05 2019-07-05 湖南速博生物技术有限公司 A kind of Pesticidal combination
CN109964940A (en) * 2018-11-14 2019-07-05 东莞东阳光科研发有限公司 A kind of application of miticide composition and its preparation, miticide composition and preparation
CN110037021A (en) * 2019-05-22 2019-07-23 侨昌现代农业有限公司 A kind of acaricidal miticide composition of Synergistic type of class containing biphenyl
CN110547299A (en) * 2019-09-02 2019-12-10 陕西上格之路生物科学有限公司 Acanenapyr-containing acaricidal composition, preparation formulation and application

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106605654A (en) * 2015-10-21 2017-05-03 陕西韦尔奇作物保护有限公司 Insecticidal composition containing SYP-9625
CN109964940A (en) * 2018-11-14 2019-07-05 东莞东阳光科研发有限公司 A kind of application of miticide composition and its preparation, miticide composition and preparation
CN109645002A (en) * 2018-12-13 2019-04-19 广东中迅农科股份有限公司 Synergetic pesticide composition containing D- limonene
CN109964948A (en) * 2019-05-05 2019-07-05 湖南速博生物技术有限公司 A kind of Pesticidal combination
CN110037021A (en) * 2019-05-22 2019-07-23 侨昌现代农业有限公司 A kind of acaricidal miticide composition of Synergistic type of class containing biphenyl
CN110547299A (en) * 2019-09-02 2019-12-10 陕西上格之路生物科学有限公司 Acanenapyr-containing acaricidal composition, preparation formulation and application

Also Published As

Publication number Publication date
CN113016812A (en) 2021-06-25

Similar Documents

Publication Publication Date Title
CN111226927B (en) Insecticidal and acaricidal composition containing mite growth inhibitor acaricide
CN111226955B (en) Insecticidal and acaricidal composition containing macrolide insect/acarid
CN111657280B (en) Insecticidal and acaricidal composition
CN111226945B (en) Synergistic insecticidal and acaricidal composition
CN111657281B (en) Insecticidal and acaricidal composition
CN111657282B (en) Insecticidal and acaricidal composition
CN113016812B (en) Insecticidal and acaricidal synergistic composition and application thereof
CN111066798A (en) Pesticide composition containing cyclic bromoantraniliprole and matrine
CN112704070B (en) Insecticidal and acaricidal composition containing pyrethroid insecticides/acaricides
CN103283731B (en) Pesticide composition for preventing and treating drug-fast tetranychid mites
CN111820237A (en) Insecticidal composition and application thereof
CN104886096B (en) Pesticidal combination and its application
CN103271042B (en) Etoxazole-hexythiazomiticide miticide composition
CN103053573B (en) Pesticide composition of metaflumizone and chromafenozide
CN106212494A (en) A kind of containing propylene glycol alginate with the composition pesticide of imidacloprid
CN109691451B (en) Insecticidal and acaricidal synergistic composition containing ethacrylonitrile and application thereof
CN115251062B (en) Synergistic insecticidal and acaricidal composition
CN103039511B (en) Bifenazate and chlorpyrifos contained synergistic acaricidal combination
CN106818888B (en) A kind of Pesticidal combination and its application containing destruxins and Nylar
CN106719657A (en) Insecticide acaricide composition and its application
CN107864962B (en) Composition containing pyriminostrobin and application thereof
CN105211091B (en) A kind of Recompounded pesticide and method for preventing and treating 2 committee noctuid insect
CN105707096B (en) Agricultural insecticidal composite
CN104273139A (en) Mite-killing composition containing fenpyroximate and ivermectin
CN115530170A (en) Insecticidal and acaricidal composition

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
TA01 Transfer of patent application right

Effective date of registration: 20210622

Address after: 110021 Shenyang Liaodong Road, Tiexi District, Shenyang, Liaoning 8-1

Applicant after: SHENYANG SINOCHEM AGROCHEMICALS R&D Co.,Ltd.

Applicant after: JIANGSU YANGNONG CHEMICAL Co.,Ltd.

Address before: 110021 Shenyang Liaodong Road, Tiexi District, Shenyang, Liaoning 8-1

Applicant before: SHENYANG SINOCHEM AGROCHEMICALS R&D Co.,Ltd.

TA01 Transfer of patent application right
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant