CN103004773A - Insecticidal composition - Google Patents
Insecticidal composition Download PDFInfo
- 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
- Authority
- CN
- China
- Prior art keywords
- pesticidal combination
- weight
- combination according
- agent
- insecticidal
- 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.)
- Pending
Links
- 0 CCN(CC1SC(Cl)=NC1)C(*)NOC Chemical compound CCN(CC1SC(Cl)=NC1)C(*)NOC 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
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
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:
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:
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
(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
(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
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.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201210572258XA CN103004773A (en) | 2012-12-25 | 2012-12-25 | Insecticidal composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201210572258XA CN103004773A (en) | 2012-12-25 | 2012-12-25 | Insecticidal composition |
Publications (1)
Publication Number | Publication Date |
---|---|
CN103004773A true CN103004773A (en) | 2013-04-03 |
Family
ID=47954304
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201210572258XA Pending CN103004773A (en) | 2012-12-25 | 2012-12-25 | Insecticidal composition |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN103004773A (en) |
Cited By (1)
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)
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 |
-
2012
- 2012-12-25 CN CN201210572258XA patent/CN103004773A/en active Pending
Patent Citations (6)
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)
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 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103300044B (en) | A kind of containing chromafenozide and the Pesticidal combination of anabasine | |
CN103283764A (en) | Cyantraniliprole containing insecticidal composition | |
CN103300000B (en) | A kind of Pesticidal combination containing ring worm hydrazides and amide-type | |
CN101836641B (en) | Oil-suspending agent disinfestation composition containing spinosyns and emamectin benzoate | |
CN102805088A (en) | Insecticidal composition as well as preparation and application thereof | |
CN101700039A (en) | Rynaxypyr and dursban insecticidal composition | |
CN102084862B (en) | Insecticidal composition containing ethiprole | |
CN102265896A (en) | Insecticidal compound containing dinotefuran and flubendiamide | |
CN102599167A (en) | Chlorantraniliprole and Spinetoram compound suspending agent and preparation method thereof | |
CN103004773A (en) | Insecticidal composition | |
CN103300035A (en) | Pesticide composition containing chromafenozide | |
CN101444221A (en) | Composition containing oxadiazine and pyrazole insecticide | |
CN102349529A (en) | Insecticidal composition containing indoxacarb and etofenprox | |
CN102365961B (en) | Insecticidal composition | |
CN102657193A (en) | Complex insecticide | |
CN103053600B (en) | Insecticidal composition of indoxacarb and efficient cyfluthrin | |
CN103238614A (en) | Insecticidal composition containing metaflumizone and cyantraniliprole | |
CN103109839B (en) | Insecticidal composition containing penta-imidacloprid guanidine and metaflumizone and preparation thereof | |
CN102696651A (en) | Spirodiclofen-containing compound pesticidal composition and preparation thereof | |
CN102273458A (en) | Pesticidal composition containing flubendiamide and nitenpyram | |
CN100433979C (en) | Compound insecticide containing fipronil and Etrofolan | |
CN104186471A (en) | Pesticide composition containing cyhalodiamide and methoxyfenozide | |
CN104094972A (en) | Composition containing sulfoxaflor and sulphur and application | |
CN104642363A (en) | A composite pesticidal composition comprising metaflumizone and spinetoram and applications thereof | |
CN103250729A (en) | Imidaclothiz and dinotefuran compound insecticide |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C12 | Rejection of a patent application after its publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20130403 |