[go: up one dir, main page]

CN116210702B - A pesticide composition containing chlorfenapyr and its application - Google Patents

A pesticide composition containing chlorfenapyr and its application Download PDF

Info

Publication number
CN116210702B
CN116210702B CN202310241852.9A CN202310241852A CN116210702B CN 116210702 B CN116210702 B CN 116210702B CN 202310241852 A CN202310241852 A CN 202310241852A CN 116210702 B CN116210702 B CN 116210702B
Authority
CN
China
Prior art keywords
pesticide composition
chlorfenapyr
formula
active ingredient
agent
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
CN202310241852.9A
Other languages
Chinese (zh)
Other versions
CN116210702A (en
Inventor
张芳
刘金玲
葛家成
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.)
Qingdao Hengning Biotechnology Co ltd
Original Assignee
Qingdao Hengning Biotechnology 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 Qingdao Hengning Biotechnology Co ltd filed Critical Qingdao Hengning Biotechnology Co ltd
Priority to CN202310241852.9A priority Critical patent/CN116210702B/en
Publication of CN116210702A publication Critical patent/CN116210702A/en
Application granted granted Critical
Publication of CN116210702B publication Critical patent/CN116210702B/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
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • 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
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/36Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01PBIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
    • A01P7/00Arthropodicides
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01PBIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
    • A01P7/00Arthropodicides
    • A01P7/04Insecticides
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

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

Abstract

The invention belongs to the field of pesticide, and relates to a pesticide composition containing chlorfenapyr and application thereof. The pesticide composition comprises a compound of the formula (I) and chlorfenapyr, wherein the mass ratio of the compound of the formula (I) to the chlorfenapyr is 1:30-28:1. The composition has the advantages of synergism, resistance reduction, safety to crops and the like, and can be used for controlling agricultural and forestry pests and sanitary pests.

Description

Pesticide composition containing chlorfenapyr and application thereof
Technical Field
The invention belongs to the technical field of pesticides, and particularly relates to a pesticide composition containing chlorfenapyr and application thereof.
Background
Chlorfenapyr (chlorfenapyr) is a novel pyrrole compound, and is a high-efficiency insecticidal and acaricidal agent developed by American cyanamide company in the late-stage of 20 th century for 80 years. 122453-73-0, the action mechanism of which is that after the insect feeds or contacts chlorfenapyr, the insect is oxidized and metabolized into a compound with insecticidal activity in the insect body, then acts on mitochondria of cells in the insect body, and the compound acts through multifunctional oxidase in the insect body, so that the conversion of Adenosine Diphosphate (ADP) to Adenosine Triphosphate (ATP) is mainly inhibited, and the adenosine triphosphate stores energy necessary for the cells to maintain the vital functions of the insect, and finally the insect is killed. The composition has stomach toxicity and contact killing effect. The plant leaf has strong penetrability on leaf surface, a certain systemic effect, and has the characteristics of broad insecticidal spectrum, high control effect, long lasting effect and safety.
The compound of the formula (I) is a methoxy acrylic ester pesticide, the CAS number is 114077-75-7, and the chemical structural formula is as follows:
in the agricultural production process, the control of various harmful insects mainly depends on the application of a large amount of pesticide products, and the pesticide is used in a large amount and frequently unreasonably, so that the drug resistance of the harmful insects is continuously enhanced, the damage to crops is more serious, and the control is more difficult. Two or more medicaments with different action mechanisms can be mixed to achieve the aim of controlling different pests, improving the control effect of the medicaments and reducing the generation of drug resistance of the pests.
In addition, in the prior art, the technical solutions of the compositions comprising the compound of formula (I) and chlorfenapyr are not specifically disclosed.
Disclosure of Invention
The invention aims to provide a pesticide composition containing chlorfenapyr, which has the advantages of synergism, reduced resistance and safety to crops.
The technical scheme adopted by the invention is that the pesticide composition containing chlorfenapyr comprises an active ingredient A and an active ingredient B, wherein the active ingredient A is a compound shown as the formula (I)
The active ingredient B is chlorfenapyr, and the mass ratio of the active ingredient A to the active ingredient B is 1:30-28:1;
Further, the mass ratio of the compound of the formula (I) to the chlorfenapyr is 1:30, 1:20, 1:8, 1:4, 3:10, 1:2, 3:5, 5:4, 6:1, 20:1, 28:1;
Further, the mass ratio of the active ingredient A to the active ingredient B is 1:20-20:1;
Further, the mass ratio of the compound of the formula (I) to the chlorfenapyr is 1:20, 1:8, 1:4, 3:10, 1:2, 3:5, 5:4, 6:1, 20:1;
further, the mass ratio of the active ingredient A to the active ingredient B is 1:8-6:1;
further, the sum of the contents of the active ingredient A and the active ingredient B in the pesticide composition is 0.5% -90% based on 100% by weight of the total mass of the pesticide composition;
further, the sum of the contents of the active ingredient A and the active ingredient B in the pesticide composition is 10% -60% based on 100% by weight of the total mass of the pesticide composition;
Further, the sum of the contents of the active ingredient A and the active ingredient B in the pesticide composition is 26%, 30%, 32%, 40%, 52% and 60% based on 100% by weight of the total mass of the pesticide composition;
further, the pesticide composition also comprises an auxiliary agent, wherein the auxiliary agent comprises a carrier and an auxiliary agent;
Further, the carrier is one or more of water, solvent or filler;
Further, the carrier is deionized water;
Further, the solvent is selected from one or more of N, N-dimethylformamide, cyclohexanone, toluene, xylene, dimethyl sulfoxide, methanol, ethanol, trimethylcyclohexanone, N-octyl pyrrolidone, ethanolamine, triethanolamine, isopropylamine, N-methylpyrrolidone, propanol, butanol, ethylene glycol, diethylene glycol, ethylene glycol methyl ether, butyl ether, ethanolamine, isopropylamine, ethyl acetate or acetonitrile;
further, the filler is selected from one or a mixture of more of kaolin, diatomite, bentonite, attapulgite, white carbon black, starch or light calcium carbonate;
the auxiliary agent at least comprises a surfactant, and other functional auxiliary agents such as an antifreezing agent, a thickening agent, a stabilizing agent, a disintegrating agent, a defoaming agent, a slow release agent, a binder and the like can be added according to different use occasions and requirements;
The surfactant is one or more selected from emulsifying agent, dispersing agent, wetting agent, dispersing medium or penetrating agent;
The surfactant is a single agent or a compound preparation of a common nonionic surfactant or an anionic surfactant, and the other functional auxiliary agents are one or more selected from antifreezing agents, thickening agents, stabilizing agents, disintegrating agents and defoaming agents;
further, the emulsifier is selected from one or more of Nongru 500# (calcium alkylbenzenesulfonate), OP series phosphate (surfactant phosphate), 600# phosphate (phenylphenol polyoxyethylene ether phosphate), styrene polyoxyethylene ether wetting agent salt, alkyl diphenyl ether disulfonate magnesium salt, triethanolamine salt, nongru 400# (benzyl dimethyl phenol polyoxyethylene ether), nongru 700# (alkylphenol formaldehyde resin polyoxyethylene ether), ningru 36# (phenethyl phenol formaldehyde resin polyoxyethylene ether), nongru 1600# (phenethyl phenol polyoxyethylene polypropylene ether), ethylene oxide-propylene oxide block copolymer, OP series (surfactant), BY series (castor oil polyoxyethylene ether), nongru 33# (alkylaryl polyoxyethylene polyoxypropylene ether), span series (sorbitan monostearate), tween series (sorbitan polyoxyethylene ether) or AEO series (fatty alcohol polyoxyethylene ether);
Further, the dispersing agent is selected from one or more of polycarboxylate, lignosulfonate, alkylphenol ethoxylate formaldehyde condensate sulfate, calcium alkylbenzenesulfonate, naphthalene sulfonate formaldehyde condensate sodium salt, alkylphenol ethoxylate, fatty amine ethoxylate, fatty acid ethoxylate or glycerin fatty acid ester ethoxylate;
further, the wetting agent is selected from one or a mixture of more of sodium dodecyl sulfate, sodium dodecyl benzene sulfonate, nekal BX, wetting penetrating agent F, chinese honeylocust fruit powder, silkworm excrement or soapberry powder;
Further, the penetrating agent is selected from one or a mixture of more of penetrating agent JFC (fatty alcohol polyoxyethylene ether), penetrating agent T (diisooctyl maleate sulfonate), azone or organic silicon;
Further, a dispersion medium such as one or more of soybean oil, rapeseed oil, wheat oil, methyl oleate, diesel oil, engine oil, mineral oil, and the like;
further, the antifreezing agent is selected from one or a mixture of more of ethylene glycol, propylene glycol, glycerol or urea;
Further, the thickener is selected from one or more of xanthan gum, disintegrating agent, bentonite, carboxymethyl cellulose or magnesium aluminum silicate;
further, the stabilizer is selected from one or a mixture of more of epoxidized soybean oil, epichlorohydrin, BHT, ethyl acetate and triphenyl phosphate;
further, the disintegrating agent is selected from one or a mixture of more of bentonite, urea, aluminum chloride, low-substituted hydroxypropyl cellulose, lactose, citric acid, succinic acid or sodium bicarbonate;
Further, the defoamer is selected from one or a mixture of more of silicone oil, silicone compounds, C10-C20 saturated fatty acid compounds or C8-C10 fatty alcohol compounds.
Further, the pesticide composition can be prepared into a pesticide acceptable preparation formulation, including solid preparations, liquid preparations, seed treatment agents and other preparations;
further, the preparation is in the form of suspending agent, water dispersible granule, aqueous emulsion, microemulsion, granule, wettable powder and dispersible oil suspending agent;
Further, the composition is prepared into a suspending agent, and the suspending agent comprises the components and the content of preferably 0.1-50% of a compound shown in the formula (I), 0.1-50% of chlorfenapyr, 2-10% of a dispersing agent, 2-10% of a wetting agent, 0.01-5% of a defoaming agent, 0-2% of a thickening agent, 0-8% of an antifreezing agent and the balance of deionized water;
Further, the composition is prepared into water dispersible granules, and the water dispersible granules comprise 0.1-50% of a compound shown in a formula (I), 0.1-50% of chlorfenapyr, 3-15% of a dispersing agent, 3-15% of a wetting agent, 1-10% of a disintegrating agent and the balance of filler;
Further, the composition is prepared into an aqueous emulsion, and the composition contains the components and the content of the components are preferably 0.1-50% of a compound shown in the formula (I), 0.1-50% of chlorfenapyr, 5-15% of an emulsifying agent, 2-10% of a solvent, 1-10% of an antifreezing agent, 0.5-3% of a stabilizing agent and the balance of deionized water;
Further, the composition is prepared into wettable powder, and the components and the content of the wettable powder are preferably 0.1-50% of a compound shown in the formula (I), 0.1-50% of chlorfenapyr, 5-20% of a wetting agent, 10-20% of a dispersing agent and 100% of a solid carrier;
further, the composition is prepared into granules, and the components and the content of the granules are preferably 0.1-50% of a compound shown in the formula (I), 0.1-50% of chlorfenapyr, 2-10% of a dispersing agent, 2-10% of a wetting agent and the balance of filler;
Further, the composition is prepared into a dispersible oil suspending agent, and the dispersible oil suspending agent comprises the components and the content of preferably 0.1% -50% of a compound shown in a formula (I), 0.1% -50% of chlorfenapyr, 1% -15% of a dispersing agent, 0.5% -20% of an emulsifying agent, 1% -10% of a wetting agent, 1% -10% of a thickening agent, 0% -10% of an antifreezing agent and the balance of a dispersing medium.
Further, the preparation formulation is any one of suspending agent and water dispersible granule.
The application of the pesticide composition containing chlorfenapyr in the aspect of controlling agricultural and forestry pests and sanitary pests;
Further, the agricultural and forestry pests and the sanitary pests are thysanoptera pests;
Further, the Thysanoptera (Thysanoptera) pests are frankliniella (Dichromothrips corbetti), dichromothrips, tabacia tabaci (FRANKLINIELLA FUSCA), alfalfa frankliniella (FRANKLINIELLA OCCIDENTALIS), oriental frankliniella (FRANKLINIELLA TRITICI), platycodon grandiflorum (Scirtothrips citri), rice Thrips (threps oryzae), palm Thrips (THRIPS PALMI) and tabaci (threps tabaci);
Further, the thysanoptera pests are frankliniella occidentalis, palmi thrips and thrips tabaci;
further, the pesticidal composition is applied to a pest to be controlled or a medium on which it grows in an effective dose.
The pesticide composition has the following advantages:
1) The composition of the invention shows synergism within a certain proportion range, and improves the control effect of the composition on pests;
2) The two active ingredients in the composition have different action mechanisms, so that the generation of drug resistance of pests is effectively delayed, and the service life of the product is prolonged;
3) The safety is high, and the method is suitable for each growth period of crops, can promote the growth of the crops, and ensures that the produced crops have higher quality.
Detailed Description
The invention will be further illustrated with reference to the following examples, in which the percentages are by weight, but the invention is not limited thereto.
The compositions of the present invention may be provided in the form of a formulation. And preparing into suspending agents, water dispersible granules and the like according to the requirements. The content of active ingredient in the composition of the invention depends on the application amount when used alone, and also on the compounding ratio and the degree of synergism. The optimum range of the active ingredient content varies depending on the type of formulation of the composition.
Formulation preparation examples:
EXAMPLE 1 32% chlorfenapyr suspension (3:5) of formula (I)
The formula comprises 12% of a compound of formula (I), 20% of chlorfenapyr, 2% of phenethyl phenol polyether phosphate, 2% of guerbet alcohol polyoxyethylene ether, 2% of sodium alkyl polyoxyethylene ether sulfonate, 1.5% of naphthalene sulfonate, 1.2% of magnesium aluminum silicate, 0.15% of xanthan gum, 0.01% of carboxyethyl cellulose, 0.05% of sodium sorbate, 5% of ethylene glycol, 0.4% of organosilicon defoamer and deionized water, wherein the balance is the balance;
the preparation method comprises the steps of sequentially placing the effective components of the compound shown in the formula (I), chlorfenapyr, a surfactant and other functional auxiliary agents in a reaction kettle according to the formula proportion, adding water, uniformly mixing, shearing at a high speed, performing wet sanding, and finally homogenizing and filtering to obtain a suspending agent product.
EXAMPLE 2 30% chlorfenapyr suspension (1:4) of formula (I)
The formula comprises 6% of compound of formula (I), 24% of chlorfenapyr, 2.5% of sodium dodecyl sulfate, 1% of naphthalene sulfonate formaldehyde condensate, 3% of styrol polyoxyethylene ether phosphate, 1% of carboxymethyl cellulose, 1.2% of magnesium aluminum silicate, 0.1% of xanthan gum, 5% of propylene glycol, 0.02% of potassium benzoate, 0.4% of organosilicon defoamer and deionized water, wherein the balance is the balance;
The preparation method is the same as in example 1.
EXAMPLE 3 26% chlorfenapyr suspension of formula (I) (3:10)
The formula comprises 6% of a compound of formula (I), 20% of chlorfenapyr, 3% of sodium lignosulfonate, 1% of naphthalene sulfonate formaldehyde condensate, 3% of alkyl polyoxyethylene ether phosphate, 1% of fatty alcohol polyoxyethylene ether, 0.5% of carboxymethyl cellulose, 1.2% of magnesium aluminum silicate, 0.15% of xanthan gum, 5% of propylene glycol, 0.02% of potassium benzoate, 0.4% of organic silicon defoamer and deionized water, wherein the balance is filled;
The preparation method is the same as in example 1.
EXAMPLE 4 40% formula (I) chlorfenapyr Water dispersible granule (1:3)
The formula comprises 10% of compound of formula (I), 30% of chlorfenapyr, 12% of sodium lignin sulfonate, 2.5% of naphthalene sulfonate formaldehyde condensate, 2% of sodium dodecyl sulfate, 4% of anhydrous sodium sulfate and the balance of kaolin;
The preparation method comprises the steps of adding the effective components into a carrier according to the proportion of an example formula, adding a surfactant and other functional additives into the carrier, mixing, adding 10-25% of water after jet milling, and then kneading, granulating, drying and screening to obtain the water dispersible granule product.
EXAMPLE 5 52% formula (I) chlorfenapyr Water dispersible granule (3:10)
The formula comprises 12% of compound of formula (I), 40% of chlorfenapyr, 8% of sodium dodecyl benzene sulfonate, 2% of sodium polycarboxylate, 3% of nekal BX, 2.5% of ammonium sulfate and the balance of starch;
The preparation method is the same as in example 4.
EXAMPLE 6 60% chlorfenapyr Water dispersible granule of formula (I) (1:2)
The formula comprises 20% of compound of formula (I), 40% of chlorfenapyr, 4% of naphthalene sulfonate formaldehyde condensate, 2% of sodium polycarboxylate, 5% of sodium dodecyl benzene sulfonate, 3% of nekal BX, 0.5% of urea and the balance of kaolin;
The preparation method is the same as in example 4.
Indoor biological Activity assay
Indoor example 1 Combined toxicity of Compounds of formula (I) and chlorfenapyr against thrips
The test method comprises a medicine film rolling tube method;
a tested insect source, namely Thrips tabaci;
The test agent is a compound original drug of the formula (I) and a chlorfenapyr original drug are provided by a group research and development center;
The preparation method comprises the steps of preparing a mother solution from an original organic solvent (acetone), and preparing 5-7 series of mass concentrations by using 0.05% -0.1% Triton X-100 (or 0.1% Tween 80) aqueous solution according to an equal ratio or an equal difference method.
The test operation steps are as follows:
The dipping tube is a glass tube with the height of 7cm and the diameter of 1.5cm, the test reagent is diluted into 5 concentrations by acetone within the concentration range determined by the pre-experiment, 250ul of reagents with each concentration are added into the glass tube by a pipette, then the glass tube is horizontally placed, and the palm is used for slowly rolling the glass tube to accelerate the volatilization of the pesticide, so that the reagents are uniformly attached on the inner wall of the glass tube. One repetition is arranged for each tube, 8 repetitions are arranged for each concentration, and an acetone immersed tube is used as a control;
leaf dipping by punching fresh cabbage leaves into 1cm diameter small discs with a punch, immersing for 10s in each concentration of the agent, and using 0.1% Tween 80 as a control. The treated leaves are placed on filter paper for airing, and are clamped into glass tubes with corresponding medicament concentration by forceps;
Transferring 25 thrips 2-year nymphs or adults into a glass tube by using a fluke device, and sealing the tube orifice by using a screen with 200 meshes.
And (3) placing the treated test insects at the temperature of 25+/-0.1 ℃ and the humidity of 60% -80% for 16h to 8h, and feeding and observing in an insect-raising room.
Investigation time is 36 hours after treatment, investigation of death condition of the test insects, and recording of total insects and dead insects.
Death criterion, namely death is counted by the fact that the tip of the writing brush dabs the insect body without reaction.
The calculation formula is as follows:
Data statistics and analysis show that the death rate of the blank control is less than 5% without correction, the death rate of the blank control is 5% -10%, the death rate of the blank control is required to be corrected, and the test is required to be carried out again when the death rate of the blank control is more than 10%.
Mixed agent theoretical toxicity index tti=ti A×PA+TIB×PB
Wherein P A、PB is the proportion of the active ingredient A, B in the composition.
Co-toxicity coefficient (CTC) CTC <80 is antagonism, CTC >120 is potentiation, and between 80 and 120 is additive.
And (3) analyzing by adopting an IBM SPSS STATISTICS statistical analysis system, solving the LC 50 value of the virulence regression line, the 95% confidence limit and the correlation coefficient R 2 of the virulence regression line, and evaluating the activity of the test agent on the biological test material.
Test results:
The results in the table 1 show that the compound of the formula (I) and the chlorfenapyr have better combined action on thrips of 2 ages, the co-toxicity coefficient of the compound of the formula (I) and the chlorfenapyr is greater than 120 when the weight ratio of the compound of the formula (I) to the chlorfenapyr is 1:30-28:1, the synergistic action is shown, the co-toxicity coefficient of the compound of the formula (I) and the chlorfenapyr is greater than 130 when the weight ratio of the compound of the formula (I) and the chlorfenapyr is 1:30-20:1, the co-toxicity coefficient of the compound of the formula (I) and the chlorfenapyr is greater than 140 when the weight ratio of the compound of the formula (I) and the chlorfenapyr is 1:20-6:1, and the synergistic action is shown to be better.
TABLE 1 results of indoor toxicity measurements of Compound of formula (I) and chlorfenapyr against thrips nymphs
The results in the table 2 show that the compound in the formula (I) and the chlorfenapyr have better combined action on adult thrips, the co-toxicity coefficient of the compound in the formula (I) and the chlorfenapyr is greater than 120 when the weight ratio of the compound in the formula (I) to the chlorfenapyr is 1:20-20:1, the synergistic action is shown, the co-toxicity coefficient of the compound in the formula (I) and the chlorfenapyr is greater than 170 when the weight ratio of the compound in the formula (I) and the chlorfenapyr is 3:10-20:1, and the synergistic action is shown, wherein the highest co-toxicity coefficient of the compound in the formula (I) and the chlorfenapyr is 225.202.
TABLE 2 indoor toxicity determination results of Compound of formula (I) and chlorfenapyr on thrips adults
Indoor toxicity results show that the compound of the formula (I) and chlorfenapyr have better prevention effect on thrips, and the weight ratio of the compound of the formula (I) to the chlorfenapyr is in the range of 1:30-28:1, so that the compound of the formula (I) and the chlorfenapyr show synergistic effect.
Safety test
Test crop and variety balsam pear Momordica CHARANTIA L (evergreen balsam pear);
the test period is the tender leaf period;
the test site is in a laboratory greenhouse of a research and development center;
the test agent comprises 30% of chlorfenapyr suspending agent (1:4) of formula (I), 60% of chlorfenapyr water dispersible granule (1:2) of formula (I), 10% of compound suspending agent of formula (I) and 240 g/L chlorfenapyr suspending agent
The specific test design comprises the following steps:
TABLE 3 safety test design
The safety measurement is that the plant growth inhibition method adopts stem and leaf spraying mode to apply the medicine for 1 time in 3-5 leaf stage (vegetative growth stage) of potted bitter gourd.
Cell area and repetition, namely random group arrangement, repeating for 4 times per treatment and 15 strains of balsam pear per treatment;
investigation of growth rate, namely respectively measuring plant height before and after the drug for 7 and 14 days;
And (3) phytotoxicity investigation, namely respectively observing and recording plant phytotoxicity conditions 7d and 14d after the phytotoxicity.
Leaf spot necrosis investigation and grading method:
Leaf no dead spot necrosis;
Slight leaf spot and leaf withering, which does not affect the normal growth of crops;
moderate leaf spot necrosis, can recover, will not cause the crop to reduce the yield;
The serious dead spot necrosis of the leaves affects the normal growth of crops, and causes a certain loss of the yield and quality of the crops;
The leaf is severely dead spot and necrotic, the crop growth is blocked, and the yield and quality loss is serious.
Deformity investigation, namely, the phytotoxicity causes the balsam pear growth point to distort and deform, which is indicated by '∈'.
And (3) data processing:
Growth rate inhibition rate:
growth rate (cm/d) =plant new growth height (cm)/time day (d);
growth rate inhibition (%) = (blank growth rate-agent treatment growth rate)/blank growth rate×100, test results:
the chlorfenapyr suspension agent with the formula (I) and the chlorfenapyr water dispersible granule with the formula (I) and the chlorfenapyr water dispersible granule with the formula (1:4) are used for 7d and 14d after being used for the test balsam pear plants, and the chlorfenapyr suspension agent with the formula (I) and the chlorfenapyr water dispersible granule with the formula (I) and the formula (1:2) have no inhibition effect.
TABLE 4 safety test results of Compounds of formula (I) and chlorfenapyr in single dose and blend on Momordica Charantia
Note that the data in the table are the average of 4 replicates, and the letters indicate significance of the differences (0.05/DMRT method)
Example of field efficacy
The compound of the formula (I) is mixed with chlorfenapyr to realize field prevention effect on thrips
Test crop and target, bitter gourd and thrips;
the test site is a greenhouse for planting balsam pears in Haiyang city of a tobacco stand in Shandong province;
test time is 2021, 6 and 20 days;
the test environment is that the cultivation conditions of all the test cells are uniform and consistent, and the same fertilizer and water management level is adopted;
Test agent:
Table 5 test design
The test method comprises applying the drug 1 time in the thrips occurrence stage.
Cell area and repetition, random block arrangement, 25 square meters per cell, 4 times per treatment.
The investigation method comprises the steps of randomly sampling five points in each district, investigating 10 balsam pear leaves in each point, hanging labels, beating thrips on the balsam pear leaves into a rice barrel paved with filter paper by using a beating method, and counting the number.
The number of insect population is investigated before the application, the survival number of each treated thrips is investigated 1 day and 7 days after the application, and the control effect is calculated respectively.
Calculation formula and data analysis:
Results of field efficacy experiments:
The test results show that 30% of the chlorfenapyr suspending agent (1:4) in the formula (I) and 60% of the chlorfenapyr water dispersible granule (1:2) in the formula (I) have good control effects on thrips, the dosage of the active ingredients is 1d and 7d after 20g ai/hm 2 of the suspending agent are applied, the control effects are over 90%, and the control effects are obvious. Wherein, when the dosage of the active ingredients of the 30% chlorfenapyr suspending agent (1:4) in the formula (I) is 30g ai/hm 2, the prevention effect of 7d after the medicine is 99.25%.
Table 6 field efficacy of Compounds of formula (I) and chlorfenapyr in preventing and controlling thrips
Note that the data in the table are the average of 4 replicates, the values remain two decimal places, and the letters indicate significance of the differences (0.05/DMRT method)
Through indoor toxicity measurement and field experiments, the pesticide composition compounded by the compound shown in the formula (I) and chlorfenapyr has a good control effect on thysanoptera pests.
The pesticide composition or the preparation prepared by the combination has remarkable prevention effect, and is superior to a single dose in the aspects of delaying the generation of drug resistance and prolonging the drug retention. In addition, no pesticide harm of the compound pesticide to crops is found in the test, which proves that the production cost and the use cost can be reduced and the pesticide composition is safe to crops under the condition that the insecticidal synergy of the obtained pesticide composition or preparation is improved.
While the invention has been described in detail in terms of the general description and the specific embodiments, it will be apparent to those skilled in the art that various modifications and improvements can be made thereto without departing from the spirit of the invention.

Claims (10)

1.一种含虫螨腈的农药组合物,其特征在于:所述的农药组合物包括活性成分A和活性成分B,所述的活性成分A为式(Ⅰ)化合物1. A pesticide composition containing chlorfenapyr, characterized in that: the pesticide composition comprises active ingredient A and active ingredient B, and the active ingredient A is a compound of formula (I) (Ⅰ),所述的活性成分B为虫螨腈,所述的活性成分A与活性成分B之间的质量比为1:20~20:1。 (I), the active ingredient B is chlorfenapyr, and the mass ratio of the active ingredient A to the active ingredient B is 1:20 to 20:1. 2.根据权利要求1所述的农药组合物,其特征在于:所述的活性成分A与活性成分B之间的质量比为1:8~6:1。2. The pesticide composition according to claim 1, characterized in that the mass ratio between the active ingredient A and the active ingredient B is 1:8~6:1. 3.根据权利要求1所述的农药组合物,其特征在于:以所述的农药组合物的总质量为100wt%计,所述的活性成分A与活性成分B在农药组合物中的含量之和为0.5%~90%。3. The pesticide composition according to claim 1, characterized in that: based on the total mass of the pesticide composition as 100wt%, the sum of the contents of the active ingredient A and the active ingredient B in the pesticide composition is 0.5% to 90%. 4.根据权利要求1所述的农药组合物,其特征在于:所述的农药组合物还包括辅助剂,所述辅助剂包括载体和助剂。4. The pesticide composition according to claim 1, characterized in that: the pesticide composition also includes an adjuvant, and the adjuvant includes a carrier and an auxiliary agent. 5.根据权利要求1所述的农药组合物,其特征在于:所述的农药组合物可以配制成农药上可接受的制剂剂型,所述的制剂剂型为悬浮剂、水分散粒剂、水乳剂、微乳剂、颗粒剂、可湿性粉剂、可分散油悬浮剂中的任一种。5. The pesticide composition according to claim 1 is characterized in that: the pesticide composition can be formulated into a pesticide acceptable formulation, and the formulation is any one of a suspension, water dispersible granules, aqueous emulsion, microemulsion, granules, wettable powder, and dispersible oil suspension. 6.根据权利要求5所述的农药组合物,其特征在于:所述的制剂剂型为悬浮剂、水分散粒剂中的任一种。6. The pesticide composition according to claim 5, characterized in that the formulation is in the form of a suspension concentrate or a water dispersible granule. 7.如权利要求1-6任一项所述的农药组合物在防治农林害虫、卫生害虫方面的应用。7. Use of the pesticide composition according to any one of claims 1 to 6 in preventing and controlling agricultural and forestry pests and sanitary pests. 8.根据权利要求7所述的应用,其特征在于:所述的农林害虫、卫生害虫为缨翅目害虫。8. The use according to claim 7, characterized in that the agricultural and forestry pests and sanitary pests are Thysanoptera pests. 9.根据权利要求8所述的应用,其特征在于:所述的缨翅目害虫为花蓟马、棕榈蓟马、烟蓟马。9. The use according to claim 8, characterized in that the Thysanoptera pests are flower thrips, palm thrips, and tobacco thrips. 10.根据权利要求9所述的应用,其特征在于:所述的农药组合物以有效剂量施于需要控制的害虫或其生长的介质上。10. The use according to claim 9, characterized in that the pesticide composition is applied to the pests to be controlled or the medium in which they grow in an effective dose.
CN202310241852.9A 2023-03-14 2023-03-14 A pesticide composition containing chlorfenapyr and its application Active CN116210702B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202310241852.9A CN116210702B (en) 2023-03-14 2023-03-14 A pesticide composition containing chlorfenapyr and its application

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202310241852.9A CN116210702B (en) 2023-03-14 2023-03-14 A pesticide composition containing chlorfenapyr and its application

Publications (2)

Publication Number Publication Date
CN116210702A CN116210702A (en) 2023-06-06
CN116210702B true CN116210702B (en) 2025-02-18

Family

ID=86571196

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202310241852.9A Active CN116210702B (en) 2023-03-14 2023-03-14 A pesticide composition containing chlorfenapyr and its application

Country Status (1)

Country Link
CN (1) CN116210702B (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104304253A (en) * 2014-09-15 2015-01-28 浙江泰达作物科技有限公司 Pesticide composition containing chlorfenapyr and picoxystrobin and its preparation and use

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11882828B2 (en) * 2015-06-02 2024-01-30 Syngenta Participations Ag Mosquito vector control compositions, methods and products utilizing same

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104304253A (en) * 2014-09-15 2015-01-28 浙江泰达作物科技有限公司 Pesticide composition containing chlorfenapyr and picoxystrobin and its preparation and use

Also Published As

Publication number Publication date
CN116210702A (en) 2023-06-06

Similar Documents

Publication Publication Date Title
CN112568224B (en) Insecticidal composition containing chlorfenapyr flubendiamide and diafenthiuron
CN116210712B (en) Insecticidal composition containing diafenthiuron and application thereof
CN116210702B (en) A pesticide composition containing chlorfenapyr and its application
CN115868502B (en) Pesticide composition containing neonicotinoid
CN115176805B (en) Pesticide composition containing spiromesifen and application thereof
CN114617129B (en) Sterilization composition and application thereof
CN114052037B (en) Acaricidal composition containing bistrifluron and etoxazole and application thereof
CN115918661B (en) Cyclobutrifluram-containing nematicidal composition and application thereof
CN112514910B (en) Insecticidal composition containing sulfoxaflor and bistrifluron
CN113796384B (en) Insecticidal composition containing bistrifluron and chlorfenapyr
CN115500354B (en) Insecticidal composition and application thereof
CN111165503A (en) Pesticide composition containing fluxapyroxad and rotenone
CN114586789B (en) Mite-killing composition and application thereof
CN112136819A (en) Bactericidal composition containing fenpicoxamid and penflufen
CN115413665B (en) Pesticide composition containing spiromesifen and application thereof
CN113317319B (en) Composite bactericide and application thereof
CN115104621B (en) Sterilization composition containing fosetyl-aluminum and application thereof
CN114271281B (en) Nematicidal composition and application thereof
CN114766492B (en) Pesticide composition containing bixafen and application thereof
CN102204555A (en) Insecticidal and acaricidal composition containing biopesticide and bifenazate
CN111466390B (en) A kind of insecticide composition containing tetrachlorantraniliprole and flupyrazone and application thereof
CN118947714A (en) An insecticide composition containing cybenzoxasulfyl and its application
CN112998027A (en) Insecticidal composition containing sulfoxaflor and cyclic bromantraniliprole
CN117770267A (en) Mite-killing composition and application thereof
CN119817586A (en) Pesticide composition containing fluopyram and application thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant