CN103004773A - Insecticidal composition - Google Patents

Insecticidal composition Download PDF

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Publication number
CN103004773A
CN103004773A CN201210572258XA CN201210572258A CN103004773A CN 103004773 A CN103004773 A CN 103004773A CN 201210572258X A CN201210572258X A CN 201210572258XA CN 201210572258 A CN201210572258 A CN 201210572258A CN 103004773 A CN103004773 A CN 103004773A
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Prior art keywords
pesticidal combination
weight
combination according
agent
insecticidal
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CN201210572258XA
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Chinese (zh)
Inventor
孔繁蕾
吴桂秀
马英高
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JIANGSU AGRICULTURAL HORMONE ENGINEERING TECHNOLOGY RESEARCH CENTRE Co Ltd
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JIANGSU AGRICULTURAL HORMONE ENGINEERING TECHNOLOGY RESEARCH CENTRE Co Ltd
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Priority to CN201210572258XA priority Critical patent/CN103004773A/en
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Abstract

The invention discloses an insecticidal composition. Active components of the insecticidal composite comprise cyantraniliprole and (E)-N-[(2-chlorine-thiazole) methyl]-N-ethyl-N'-methoxy-2-nitryl vinylidene diamine in a weight ratio of (1:0.1) to (1:10), and the total weight of the active components accounts for 2%-80% of the insecticidal composition. The insecticidal composition provided by the invention has complementary insecticidal efficacy, expands an insecticidal spectrum, has a higher control effect on armyworms, aphids, mosquitoes and striped rice borer in comparison with single cyantraniliprole, has remarkable synergism and a good insecticidal fast-acting property, and has the advantage of low cost.

Description

Pesticidal combination
Technical field
The present invention relates to a kind of Pesticidal combination.
Background technology
The chemical name of bromine cyanogen insect amide (have another name called cyanogen insect amide, the CAS accession number is 736994-63-1) is: 3-bromo-N-[4-cyano group-2-methyl-6-(methylamine formoxyl)-and phenyl]-1-(3-chloropyridine-2 base)-1H-pyrazoles-5-formamide.Structural formula is as follows:
Figure BDA00002646260600011
The bromine cyanogen insect amide belongs to benzamides insect ryanodine receptor inhibitor, and mainly by inducing the insect ryanodine receptor, the regulation and control intracellular calcium ion discharges and shows and tag and stomach poison function.Be mainly used in the insects such as crop control snout moth's larva, plant hopper, leafhopper such as paddy rice, vegetables, fruit tree, cotton.
Chinese patent literature 102633740A discloses a kind of anabasine compound and its preparation method and application, wherein embodiment 1 discloses a kind of compound: (E)-N-[(2-chloro-thiazole) methyl]-N-ethyl-N '-methoxyl group-2-nitro ethenylidene diamines, its structural formula is as follows:
Figure BDA00002646260600012
This compound belongs to second generation nicotinic insecticide, is the nAChR antagonist, affects the transmission of insect central nervous system choline.Be mainly used in the insects such as the crops such as paddy rice, fruit tree, vegetables and tealeaves prevent eliminating aphis, leafhopper, plant hopper.
At present, not yet find the bromine cyanogen insect amide with (E)-N-[(2-chloro-thiazole) methyl] the composite report of N-ethyl-N '-methoxyl group-2 nitro ethenylidene diamines.
Summary of the invention
The object of the invention is to address the above problem, provide a kind of and have obvious synergistic effect, quick-acting is good, insecticidal spectrum is wide, lower-cost Pesticidal combination.
The technical scheme that realizes the object of the invention is: a kind of Pesticidal combination, active component is by bromine cyanogen insect amide and (E) N--[(2-chloro-thiazole) methyl]-N-ethyl-N '-methoxyl group-2-nitro ethenylidene diamines forms.
The bromine cyanogen insect amide with (E)-N-[(2-chloro-thiazole) methyl]-weight ratio of N-ethyl-N '-methoxyl group-2-nitro ethenylidene diamines is 1: 0.1~1: 10.
Described active component gross weight is 2%~80% of Pesticidal combination gross weight.
This Pesticidal combination is made the upper applicable arbitrary formulation of agricultural by adding auxiliary agent and carrier, such as wetting powder, granule, suspending agent, microemulsion, soluble granule etc.
Take wetting powder as example, this Pesticidal combination is also to have following component except above-mentioned active component: be 1%~10% dispersant of composition total weight; 2%~5% wetting agent for composition total weight; 0.5%~5% stabilizing agent for composition total weight; 1%~80% carrier for composition total weight.
Described dispersant is a kind of in sodium lignin sulfonate, sodium naphthalene sulfonate or the naphthalene sulfonic acids calcium or two kinds; Described wetting agent is a kind of in lauryl sodium sulfate, sodium butylnaphthalenesulfonate, sldium lauryl sulfate, dodecyl sodium sulfate or the neopelex or two kinds; Described stabilizing agent is a kind of in hydroxypropyl cellulose, carboxymethyl cellulose or the epoxidized soybean oil or two kinds; Described carrier is a kind of in diatomite, potter's clay or the bentonite or two kinds.
The good effect that the present invention has: (1) Pesticidal combination insecticidal effect of the present invention is complementary, has widened insecticidal spectrum.And the control efficiency of mythimna separata, aphid, mosquito and striped rice borer is higher than bromine cyanogen insect amide single dose, have obvious synergistic effect, and desinsection quick-acting is good.(2) because (E)-N-[(2-chloro-thiazole) methyl]-price of N-ethyl-N '-methoxyl group-2-nitro ethenylidene diamines only has about 1/9 of bromine cyanogen insect amide, therefore Pesticidal combination of the present invention also has lower-cost advantage.(3) dispenser of Pesticidal combination of the present invention can prevent and treat various pests, is the substitute of high-toxic pesticide.
Embodiment
(embodiment 1)
The formulation of the Pesticidal combination of the present embodiment is wetting powder, is made by the component of following weight:
Bromine cyanogen insect amide 10g as active component;
(E)-N-[(2-chloro-thiazole as active component) methyl]-N-ethyl-N '-methoxyl group-2-nitro ethenylidene diamines 10g;
Sodium lignin sulfonate 8g as dispersant;
Lauryl sodium sulfate 3.5g as wetting agent;
Hydroxypropyl cellulose 3g as stabilizing agent;
Diatomite 65.5g as carrier.
The preparation method is: according to above-mentioned prescription, first with bromine cyanogen insect amide and (E)-N-[(2-chloro-thiazole) methyl] N--ethyl-N '-methoxyl group-2-nitro ethenylidene diamines joins in the cracker of 250mL and then adds successively sodium lignin sulfonate, SDS, hydroxypropyl cellulose and diatomite, behind the co-grinding, through ultramicro grinding to particle diameter greater than 200 purpose wetting powders.
(embodiment 2~embodiment 9)
Each embodiment is substantially the same manner as Example 1, and difference sees Table 1.(E)-N-[(2-chloro-thiazole wherein) methyl]-N-ethyl-N '-methoxyl group-2-nitro ethenylidene diamines represents by anabasine compound.
Table 1
Figure BDA00002646260600031
(experimental example 1)
This experimental example is given birth to the survey experiment to mythimna separata, aphis craccivora, Culex pipiens pallens and striped rice borer respectively for the Pesticidal combination and the bromine cyanogen insect amide single dose that adopt embodiment 1.Investigate respectively the one day after dead borer population of all striped rice borer behind the dead borer population of two days mythimna separatas and the medicine behind the dead borer population, medicine of aphis craccivora and Culex pipiens pallens of medicine, and calculate lethality.Concrete outcome table 2.
Table 2
Figure BDA00002646260600041
(experimental example 2)
This experimental example is for investigation and calculate the lethality of respectively testing target, and carries out statistical analysis with data handling system (DPS) software, calculates the LC of each medicament 50, r value etc. and 95% confidence limit thereof.
Take the Pesticidal combination of embodiment 1 to the aphis craccivora medication as example, investigation different tests concentration, the death condition of two days aphis craccivoras behind the medicine, and calculate lethality and carry out corresponding statistical analysis the results are shown in Table 3.
Table 3
Figure BDA00002646260600042
Adopt the Pesticidal combination of similar approach difference statistical analysis embodiment 1 to other insect, and bromine cyanogen insect amide single dose specifically see Table 4 to the experimental result of each insect.
Table 4
Insecticide Insect Regression equation LC 50 r 95% confidence limit
Embodiment 1 Striped rice borer Y=3.29+1.06x 40.98 0.9904 31.84~52.73
Bromine cyanogen insect amide single dose Striped rice borer Y=3.48+0.93x 43.77 0.9958 33.00~58.06
Embodiment 1 Aphis craccivora Y=3.87+1.43x 6.18 0.9993 5.12~7.46
Bromine cyanogen insect amide single dose Aphis craccivora Y=2.49+2.03x 17.15 0.9984 14.80~19.88
Embodiment 1 Culex pipiens pallens Y=4.43+3.00x 1.55 0.9985 1.39~1.72
Bromine cyanogen insect amide single dose Culex pipiens pallens Y=3.75+1.83x 4.81 0.9997 4.13~5.61
As shown in Table 4: for striped rice borer, aphis craccivora and Culex pipiens pallens, the LC of the Pesticidal combination of embodiment 1 50Value is all less than the LC of bromine cyanogen insect amide single dose 50Value.Illustrate that the insecticidal activity of Pesticidal combination of embodiment 1 is all greater than bromine cyanogen insect amide single dose.

Claims (9)

1. Pesticidal combination is characterized in that: active component by the bromine cyanogen insect amide with (E)-N-[(2-chloro-thiazole) methyl]-N-ethyl-N '-methoxyl group-2-nitro ethenylidene diamines forms.
2. Pesticidal combination according to claim 1 is characterized in that: the bromine cyanogen insect amide with (E)-N-[(2-chloro-thiazole) methyl]-weight ratio of N-ethyl-N '-methoxyl group-2-nitro ethenylidene diamines is 1: 0.1~1: 10.
3. Pesticidal combination according to claim 2, it is characterized in that: described active component gross weight is 2%~80% of Pesticidal combination gross weight.
4. Pesticidal combination according to claim 1, it is characterized in that: described active component gross weight is 2%~80% of Pesticidal combination gross weight.
5. according to claim 1 to one of 4 described Pesticidal combinations, it is characterized in that: this Pesticidal combination is made the upper applicable arbitrary formulation of agricultural by adding auxiliary agent and carrier.
6. Pesticidal combination according to claim 5, it is characterized in that: the formulation of said composition is wetting powder, granule, suspending agent, microemulsion or soluble granule.
7. Pesticidal combination according to claim 6, it is characterized in that: the formulation of said composition is wetting powder; Described auxiliary agent is dispersant, wetting agent and stabilizing agent.
8. Pesticidal combination according to claim 7, it is characterized in that: the weight of described dispersant is 1%~10% of composition total weight; The weight of described wetting agent is 2%~5% of composition total weight; The weight of described stabilizing agent is 0.5%~5% of composition total weight; The weight of described carrier is 1%~80% of composition total weight.
9. Pesticidal combination according to claim 8 is characterized in that: described dispersant is a kind of in sodium lignin sulfonate, sodium naphthalene sulfonate or the naphthalene sulfonic acids calcium or two kinds; Described wetting agent is a kind of in lauryl sodium sulfate, sodium butylnaphthalenesulfonate, sldium lauryl sulfate, dodecyl sodium sulfate or the neopelex or two kinds; Described stabilizing agent is a kind of in hydroxypropyl cellulose, carboxymethyl cellulose or the epoxidized soybean oil or two kinds; Described carrier is a kind of in diatomite, potter's clay or the bentonite or two kinds.
CN201210572258XA 2012-12-25 2012-12-25 Insecticidal composition Pending CN103004773A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111903673A (en) * 2020-09-01 2020-11-10 福建省三明市烟草物流有限责任公司 Diatomite and ryanodine receptor inhibitor insecticidal composition, preparation method thereof and application thereof in preventing and controlling tobacco stem borers

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1988803A (en) * 2004-07-26 2007-06-27 杜邦公司 Mixtures of anthranilamide invertebrate pest control agents
CN102633740A (en) * 2012-02-29 2012-08-15 江苏省农用激素工程技术研究中心有限公司 Anabasine compound, preparation method and application of nabasine compound
CN102630696A (en) * 2012-04-05 2012-08-15 广西田园生化股份有限公司 Insecticidal composite containing Cyantraniliprole and anabasine compounds
CN102657177A (en) * 2012-04-18 2012-09-12 联保作物科技有限公司 Insecticidal composition and preparation and application thereof
CN102696656A (en) * 2012-06-11 2012-10-03 联保作物科技有限公司 Insecticidal composition and preparation thereof
CN102805099A (en) * 2012-08-23 2012-12-05 北京燕化永乐农药有限公司 Insect disinfestation composition

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1988803A (en) * 2004-07-26 2007-06-27 杜邦公司 Mixtures of anthranilamide invertebrate pest control agents
CN102633740A (en) * 2012-02-29 2012-08-15 江苏省农用激素工程技术研究中心有限公司 Anabasine compound, preparation method and application of nabasine compound
CN102630696A (en) * 2012-04-05 2012-08-15 广西田园生化股份有限公司 Insecticidal composite containing Cyantraniliprole and anabasine compounds
CN102657177A (en) * 2012-04-18 2012-09-12 联保作物科技有限公司 Insecticidal composition and preparation and application thereof
CN102696656A (en) * 2012-06-11 2012-10-03 联保作物科技有限公司 Insecticidal composition and preparation thereof
CN102805099A (en) * 2012-08-23 2012-12-05 北京燕化永乐农药有限公司 Insect disinfestation composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111903673A (en) * 2020-09-01 2020-11-10 福建省三明市烟草物流有限责任公司 Diatomite and ryanodine receptor inhibitor insecticidal composition, preparation method thereof and application thereof in preventing and controlling tobacco stem borers

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Application publication date: 20130403