CN103843804A - Fungicidal composition containing ametoctradin - Google Patents

Fungicidal composition containing ametoctradin Download PDF

Info

Publication number
CN103843804A
CN103843804A CN201210521269.5A CN201210521269A CN103843804A CN 103843804 A CN103843804 A CN 103843804A CN 201210521269 A CN201210521269 A CN 201210521269A CN 103843804 A CN103843804 A CN 103843804A
Authority
CN
China
Prior art keywords
azoles mepanipyrim
azoles
weight ratio
mepanipyrim
composition containing
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
Application number
CN201210521269.5A
Other languages
Chinese (zh)
Inventor
张秋芳
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.)
Shanxi Thompson Biological Technology Co Ltd
Original Assignee
Shanxi Thompson Biological Technology 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 Shanxi Thompson Biological Technology Co Ltd filed Critical Shanxi Thompson Biological Technology Co Ltd
Priority to CN201210521269.5A priority Critical patent/CN103843804A/en
Publication of CN103843804A publication Critical patent/CN103843804A/en
Pending legal-status Critical Current

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The invention discloses a fungicidal composition containing ametoctradin. The fungicidal composition contains an active ingredient A and an active ingredient B, wherein the active ingredient A is selected from ametoctradin, the active ingredient B is selected from any one of the following compounds: thiophanate-methyl, cyazofamid, triflumizole, fenamidone, carbendazim, prochloraz and salts thereof, and the weight ratio of the active ingredient A to the active ingredient B is (1: 80)-(80: 1). The composition disclosed by the invention has synergy against a variety of diseases in agricultural production, and can reduce the dosage of a pesticide, reduce the residual amount of the pesticide on crops, reduce environmental pollution, realize safety to people and animals and good environmental compatibility and enable the diseases to be less prone to producing drug resistance.

Description

A kind of bactericidal composition containing azoles mepanipyrim
Technical field
The invention belongs to technical field of pesticide, relate to the application of a kind of bactericidal composition containing azoles mepanipyrim on corps diseases.
Background technology
Azoles mepanipyrim (ametoctradin) is obtained interim registration in China, and azoles mepanipyrim is brand-new triazolo pyrimidine series bactericidal agent, for the downy mildew of prevention and control cucumber and grape crop.
Thiophanate-methyl, cyazofamid, fluorine bacterium azoles, Fenamidone, carbendazim, Prochloraz or its salt all belong to common fungicide, are widely used in the disease of crops, and wherein the salt of Prochloraz comprises prochloraz-manganese chloride complex, prochloraz nantokite, prochloraz zinc salt.
But in the real process of agricultural production, preventing and treating the problem that disease the most easily produces is the generation of disease drug resistance.Different cultivars composition carries out composite, is to prevent and treat the very common method of resistance disease.Heterogeneity is carried out composite, according to practical application effect, judge certain composite be synergy, add and or antagonism.In most cases, the composite effect of sterilization is all additive effect, really have a synergistic effect composite seldom, especially synergistic effect very obviously, synergy ratio very high composite just still less.Through inventor's research, find azoles mepanipyrim and thiophanate-methyl, cyazofamid, fluorine bacterium azoles, Fenamidone, carbendazim, Prochloraz or its salt can produce good synergistic effect after composite, and not yet open about azoles mepanipyrim and the composite relevant report of thiophanate-methyl, cyazofamid, fluorine bacterium azoles, Fenamidone, carbendazim, Prochloraz or its salt.
Summary of the invention
The object of the invention is to propose a kind of have synergistic function, use cost is low, preventive effect the is good bactericidal composition containing azoles mepanipyrim.
The bactericidal composition containing azoles mepanipyrim that the present invention proposes contains active components A and active component B, activity is divided into A and active component B weight ratio is 1 ︰ 80 ~ 80 ︰ 1, described active components A is selected from azoles mepanipyrim, active component B is selected from the one in thiophanate-methyl, cyazofamid, fluorine bacterium azoles, Fenamidone, carbendazim, Prochloraz or its salt, and active components A and the preferred weight ratio of active component B are 1 ︰ 50 ~ 50 ︰ 1; More preferably the weight ratio of azoles mepanipyrim and thiophanate-methyl is 1 ︰ 25 ~ 20 ︰ 1, the weight ratio of azoles mepanipyrim and cyazofamid or Fenamidone is 1 ︰ 20 ~ 25 ︰ 1, the weight ratio of azoles mepanipyrim and fluorine bacterium azoles is 1 ︰ 25 ~ 30 ︰ 1, the weight ratio of azoles mepanipyrim and carbendazim is 1 ︰ 30 ~ 25 ︰ 1, and the weight ratio of azoles mepanipyrim and Prochloraz or its salt is 1 ︰ 30 ~ 30 ︰ 1; The weight ratio that most preferably is azoles mepanipyrim and thiophanate-methyl is 1 ︰ 9 ~ 4 ︰ 1, the weight ratio of azoles mepanipyrim and cyazofamid or Fenamidone is 1 ︰ 4 ~ 9 ︰ 1, the weight ratio of azoles mepanipyrim and fluorine bacterium azoles is 1 ︰ 5 ~ 11 ︰ 1, the weight ratio of azoles mepanipyrim and carbendazim is 1 ︰ 9 ~ 4 ︰ 1, and the weight ratio of azoles mepanipyrim and Prochloraz or its salt is 1 ︰ 5 ~ 5 ︰ 1.
The bactericidal composition containing azoles mepanipyrim that the present invention proposes is for preventing and treating the purposes of disease on crops, and described crops comprise cereal crops, legume crop, fiber crop, sugar [yielding, melon crop, fruits crop, dry fruit crop, hobby crop, root crop, oil crop, flowers crop, medicinal crop, raw material crop, green manure pasture crop; Described disease comprises downy mildew, epidemic disease, scab, powdery mildew, anthracnose, peronospora tabacina, head blight, damping off, spot defoliation, rice blast, brown spot, stalk break, leaf mold, leaf rot, banded sclerotial blight, shot hole, rust, green mould or penicilliosis.
The weight ratio of active components A, active component B is 1 ︰ 80 ~ 80 ︰ 1.Conventionally in composition, the weight percentage of active component is gross weight 0.5%~90%, is preferably 5%~80%.According to different preparation types, active component content scope is different.Conventionally, liquid preparation contains 1%~70% active substance by weight, is preferably 5%~50%; Solid pharmaceutical preparation contains 5%~80% active substance by weight, is preferably 10%~80%.
In bactericidal composition of the present invention, at least contain a kind of surfactant, the dispersion of active component in water while being beneficial to use.Surface-active contents is 5%~30% of total formulation weight amount, and surplus is solid or liquid diluent.
Bactericidal composition of the present invention can be by user before use through dilution or directly use.Its preparation can be prepared by common processing method known in those skilled in the art, after mixing with liquid flux or solid carrier by active substance, then add surfactant as one or more in dispersant, stabilizing agent, wetting agent, binding agent, defoamer, disintegrant, antifreeze etc.
Bactericidal composition of the present invention, can be processed on demand acceptable formulation in any sterilization, wherein more preferably formulation is wetting powder, water dispersible granules, suspending agent, suspension emulsion, aqueous emulsion, microemulsion, microcapsule suspending agent, microcapsule suspension-suspending agent.
When making wetting powder, composition comprises following constituent content: active components A 1% ~ 80%, active component B1% ~ 80%, dispersant 2% ~ 10%, wetting agent 2% ~ 10%, filler surplus.
When making water dispersible granules, composition comprises following constituent content: active components A 1% ~ 80%, active component B1% ~ 80%, dispersant 3% ~ 12%, wetting agent 1% ~ 8%, disintegrant 1% ~ 10%, binding agent 0 ~ 8%, filler surplus.
When making suspending agent, composition comprises following constituent content: active components A 0.5% ~ 50%, active component B0.5% ~ 50%, dispersant 2% ~ 10%, wetting agent 2% ~ 10%, defoamer 0.01% ~ 2%, thickener 0 ~ 2%, antifreeze 0 ~ 8%, deionized water add to 100%.
When making suspension emulsion, composition comprises following constituent content: active components A 0.5% ~ 50%, active component B0.5% ~ 50%, dispersant 2% ~ 10%, defoamer 0.01% ~ 2%, solvent 1% ~ 15%, thickener 0 ~ 2%, emulsifier 2% ~ 12%, antifreeze 0 ~ 8%, deionized water add to 100%.
When making aqueous emulsion, composition comprises following constituent content: active components A 0.5% ~ 50%, active component B0.5% ~ 50%, solvent 1% ~ 30%, emulsifier 1% ~ 15%, antifreeze 0 ~ 8%, thickener 0 ~ 2%, defoamer 0.01% ~ 2%, deionized water are supplied surplus.
When making microemulsion, composition comprises following constituent content: active components A 0.5% ~ 50%, active component B0.5% ~ 50%, solvent 1% ~ 30%, emulsifier 3% ~ 25%, antifreeze 0 ~ 8%, defoamer 0.01% ~ 2%, deionized water are supplied surplus.
When making microcapsule suspending agent, composition comprises following constituent content: active components A 0.5% ~ 50%, active component B0.5% ~ 50%, macromolecule cyst material 2% ~ 10%, dispersant 1% ~ 10%, organic solvent 1% ~ 10%, emulsifier 1% ~ 7%, defoamer 0.01% ~ 2%, pH adjusting agent 0.01% ~ 5%, deionized water add to 100%.
When making microcapsule suspension-suspending agent, composition comprises following constituent content: active components A 0.5% ~ 50%, active component B0.5% ~ 50%, macromolecule cyst material 2% ~ 10%, dispersant 1% ~ 12%, wetting agent 1% ~ 8%, organic solvent 1% ~ 15%, emulsifier 1% ~ 6%, defoamer 0.01% ~ 2%, thickener 0 ~ 2%, pH adjusting agent 0.01% ~ 5%, deionized water add to 100%;
Wetting powder the key technical indexes of the present invention:
Figure BDA00002538973600051
Water dispersible granules the key technical indexes of the present invention:
Figure BDA00002538973600052
Suspending agent the key technical indexes of the present invention:
Figure BDA00002538973600053
Suspension emulsion the key technical indexes of the present invention:
Aqueous emulsion the key technical indexes of the present invention:
Figure BDA00002538973600055
Microemulsion the key technical indexes of the present invention:
Microcapsule suspending agent the key technical indexes of the present invention:
Microcapsule suspension-suspending agent the key technical indexes of the present invention:
Figure BDA00002538973600063
The invention has the advantages that:
(1) azoles mepanipyrim and thiophanate-methyl, cyazofamid, fluorine bacterium azoles, Fenamidone, carbendazim, Prochloraz or its salt composite after, there is obvious synergy and lasting effect; (2) disease on cereal crops, legume crop, fiber crop, sugar [yielding, melon crop, fruits crop, dry fruit crop, hobby crop, root crop, oil crop, flowers crop, medicinal crop, raw material crop, green manure pasture crop is all had to greater activity; (3) reduce agricultural chemicals dosage, reduced the residual quantity of agricultural chemicals on crop, alleviated environmental pollution; (4), to person poultry safety, Environmental compatibility is good; And preparation adhesion strength strengthens, resistance of rainwater washing against.
Embodiment
Below in conjunction with embodiment, to further instruction of the present invention, the percentage in embodiment is all weight percentage, but the present invention is not limited thereto.
Application Example one
Embodiment 1~16 wetting powder
Azoles mepanipyrim, active component B, dispersant, wetting agent, filler are mixed in mixed cylinder, after airslide disintegrating mill is pulverized, mix again, can make wetting powder product of the present invention, specifically in table 1.
The each component of table 1 embodiment 1~16 and weight portion
Figure BDA00002538973600071
Figure BDA00002538973600081
Embodiment 17~32 water dispersible granules
Azoles mepanipyrim, active component B, dispersant, wetting agent, disintegrant, filler etc. are obtained to the particle diameter needing through air-flow crushing together, then add other auxiliary agents such as binding agent (can add and can not add), obtain the materials of granulating.By item quantitatively send in fluidized bed granulation dryer through granulation and dry after, can make water dispersible granules product of the present invention, specifically in table 2.
The each component of table 2 embodiment 17~32 and weight portion
Figure BDA00002538973600082
Figure BDA00002538973600091
By thiophanate-methyl, cyazofamid, fluorine bacterium azoles, Fenamidone, carbendazim, Prochloraz or its salt interchange in table 1,2, can make novel formulation.
Embodiment 33~48 suspending agents
By dispersant, wetting agent, defoamer, thickener (can add and can not add), antifreeze (can add and can not add), mix through high speed shear, add azoles mepanipyrim, active component B, ball milling 2 ~ 3 hours in ball mill, make diameter of particle all below 5 μ m, surplus is supplied by deionized water, can make suspending agent product of the present invention, specifically in table 3.
The each component of table 3 embodiment 33~48 and weight portion
Figure BDA00002538973600101
Embodiment 49~56 suspension emulsions
Dispersant, defoamer, thickener (can add and can not add), antifreeze (can add and can not add) are mixed through high speed shear, add azoles mepanipyrim, ball milling 2 ~ 3 hours in ball mill, make diameter of particle all below 5 μ m, make azoles mepanipyrim suspending agent, then by active component B, solvent, emulsifier and various auxiliary agent with the direct emulsification of high speed agitator in suspending agent, surplus is supplied by deionized water, make suspension emulsion product of the present invention, specifically in table 4,5.
The each component of table 4 embodiment 49~52 and weight portion
Figure BDA00002538973600111
The each component of table 5 embodiment 53~56 and weight portion
Figure BDA00002538973600112
Embodiment 57~66 aqueous emulsions
Azoles mepanipyrim, active component B, solvent, emulsifier are added together, make to be dissolved into even oil phase; Deionized water, antifreeze (can add and can not add), thickener (can add and can not add), defoamer are mixed, become homogeneous water.Under high-speed stirred, water is added to oil phase, surplus is supplied by deionized water; Can make aqueous emulsion product of the present invention, specifically in table 6.
The each component of table 6 embodiment 57~66 and weight portion
Figure BDA00002538973600121
Thiophanate-methyl, cyazofamid, fluorine bacterium azoles, Fenamidone, carbendazim, Prochloraz in table 3 ~ 6 are exchanged, can make novel formulation.
Embodiment 67~69 microemulsions
Azoles mepanipyrim, active component B, solvent, emulsifier, antifreeze (can add and can not add), defoamer are fully mixed into the oil phase of homogeneous transparent, under agitation slowly add deionized water, form WO emulsion, again through agitating heating, make it rapid phase inversion and become oil-in-water type, be chilled to room temperature and make it to reach balance, after filtration, surplus is supplied by deionized water; Can make microemulsion product of the present invention, specifically in table 7.
The each component of table 7 embodiment 67~69 and weight portion
Figure BDA00002538973600131
Embodiment 70,71 microcapsule suspending agents
By azoles mepanipyrim, active component B, macromolecule cyst material, solvent, make to be dissolved into even oil phase, under shearing condition, oil phase is joined in the aqueous phase solution that contains emulsifier, pH adjusting agent, dispersant, surplus is supplied by deionized water, bi-material reacts at oil-water interfaces, forms macromolecule cyst wall, makes the finely disseminated microcapsule suspending agent product of the present composition.Specifically in table 8.
Table 8 embodiment 70,71 each component and weight portions
Figure BDA00002538973600132
Embodiment 72,73 microcapsule suspensions-suspending agent
By active component B, macromolecule cyst material, solvent, make to be dissolved into even oil phase, oil phase is joined in the aqueous phase solution that contains emulsifier, pH adjusting agent under shearing condition, make finely disseminated microcapsule suspending agent.Dispersant, wetting agent, defoamer, thickener (can add and can not add) are mixed through high speed shear, add azoles mepanipyrim, ball milling 2 ~ 3 hours in ball mill, make diameter of particle all below 5 μ m, make suspending agent, then suspending agent is joined in the aqueous phase solution of micro-capsule suspension, deionized water is supplied surplus, make the finely disseminated microcapsule suspension-suspending agent of present composition product, specifically in table 9.
Table 9 embodiment 72,73 each component and weight portions
Figure BDA00002538973600141
The embodiment of the present invention is the method that adopts Toxicity Determination and field trial to combine.First by Toxicity Determination, the synergy ratio (SR) after clear and definite two kinds of medicaments are composite by a certain percentage, SR < 0.5 is antagonism, 0.5≤SR≤1.5 are summation action, SR > 1.5 is synergistic effect, on this basis, then carries out field trial.
Test method: after the effective inhibition concentration scope of each medicament is determined in prerun, medicament is established respectively 5 dosage processing by active constituent content, establishes clear water contrast.Carry out with reference to " farm-chemical indoor determination test rule bactericide ", adopt mycelial growth rate method to measure the virulence of medicament to crop germ.After 72h, measure colony diameter by right-angled intersection method, calculate each processing net growth, mycelial growth inhibition rate.
Net growth (mm)=measurement colony diameter-5
Figure BDA00002538973600151
Mycelial growth inhibition rate is converted into probit value (y), and liquor strength (μ g/mL) converts logarithm value to (x), tries to achieve virulence regression equation (y=a+bx) with method of least squares, and calculates thus the EC of every kind of medicament 50value.Calculate the different proportioning synergy ratios of two medicaments (SR) according to Wadley method, SR < 0.5 is antagonism simultaneously, and 0.5≤SR≤1.5 are summation action, and SR > 1.5 is synergistic effect.Computing formula is as follows:
Figure BDA00002538973600152
Figure BDA00002538973600153
Wherein: a, b are respectively active components A and active component B shared ratio in combination;
A is azoles mepanipyrim;
B is selected from the one in thiophanate-methyl, cyazofamid, fluorine bacterium azoles, Fenamidone, carbendazim, Prochloraz or its salt.
Application Example two:
For trying disease: powdery mildew of cucumber
Test medicine provides by Shanxi Thompson Biological Technology Co., Ltd..
Experimental scheme: effective inhibition concentration scope of determining azoles mepanipyrim and thiophanate methyl raw pesticide and the two different proportioning mixture through preliminary experiment.
Toxicity test result
The composite toxicity test analysis of results table to powdery mildew of cucumber of table 10 azoles mepanipyrim and thiophanate-methyl
Figure BDA00002538973600161
As shown in Table 10, azoles mepanipyrim and the thiophanate-methyl proportioning synergy ratio SR to powdery mildew of cucumber in the time of 1 ︰ 80 ~ 80 ︰ 1 is all greater than 1.5, illustrate that both all show synergistic effect at mixture in 1 ︰ 80 ~ 80 ︰ 1 scopes, when the proportioning of azoles mepanipyrim and thiophanate-methyl is during at 1 ︰ 25 ~ 20 ︰ 1, synergistic effect is more outstanding, and synergy ratio is all more than 2.25.Test and find that the optimum ratio of azoles mepanipyrim and thiophanate-methyl is 20:1,15:1,10:1,8:1,6:1,4:1,3:1,2:1,1:1,1:2,1:3,1:4,1:5,1:6,1:7,1:8,1:10,1:15,1:20,1:25 through applicant, especially synergy ratio maximum in the time that azoles mepanipyrim and thiophanate-methyl weight ratio are 1:2, synergistic effect is the most obvious.
Application Example three
For trying disease: cucumber downy mildew
Test medicine provides by Shanxi Thompson Biological Technology Co., Ltd..
Experimental scheme: effective inhibition concentration scope of determining the former medicine of azoles mepanipyrim and cyazofamid and the two different proportioning mixture through preliminary experiment.
The composite toxicity test analysis of results table to cucumber downy mildew of table 11 azoles mepanipyrim and cyazofamid
Figure BDA00002538973600171
As shown in Table 11, azoles mepanipyrim and the cyazofamid proportioning synergy ratio SR to cucumber downy mildew in the time of 1 ︰ 80 ~ 80 ︰ 1 is all greater than 1.5, illustrate that both all show synergistic effect at mixture in 1 ︰ 80 ~ 80 ︰ 1 scopes, when the proportioning of azoles mepanipyrim and cyazofamid is during at 1 ︰ 20 ~ 25 ︰ 1, synergistic effect is more outstanding, and synergy ratio is all more than 2.20.Test and find that the optimum ratio of azoles mepanipyrim and cyazofamid is 25:1,20:1,15:1,10:1,8:1,7:1,6:1,5:1,4:1,3:1,2:1,1:1,1:2,1:3,1:4,1:5,1:6,1:8,1:10,1:12,1:15,1:20 through applicant, especially synergy ratio maximum in the time that azoles mepanipyrim and cyazofamid weight ratio are 2:1, synergistic effect is the most obvious.
Application Example four
For trying disease: pear scab
Test medicine provides by Shanxi Thompson Biological Technology Co., Ltd..
Experimental scheme: effective inhibition concentration scope of determining azoles mepanipyrim and the former medicine of fluorine bacterium azoles and the two different proportioning mixture through preliminary experiment.
The composite toxicity test analysis of results table to pear scab of table 12 azoles mepanipyrim and fluorine bacterium azoles
Figure BDA00002538973600181
As shown in Table 12, azoles mepanipyrim and the fluorine bacterium azoles proportioning synergy ratio SR to pear scab in the time of 1 ︰ 80 ~ 80 ︰ 1 is all greater than 1.5, illustrate that both all show synergistic effect at mixture in 1 ︰ 80 ~ 80 ︰ 1 scopes, when the proportioning of azoles mepanipyrim and fluorine bacterium azoles is during at 1 ︰ 25 ~ 30 ︰ 1, synergistic effect is more outstanding, and synergy ratio is all more than 2.15.Test and find that the optimum ratio of azoles mepanipyrim and fluorine bacterium azoles is 30:1,20:1,10:1,8:1,7:1,6:1,5:1,4:1,3:1,2:1,1:1,1:2,1:3,1:4,1:5,1:8,1:10,1:15,1:20,1:25 through applicant, especially synergy ratio maximum in the time that azoles mepanipyrim and fluorine bacterium azoles weight ratio are 3:1, synergistic effect is the most obvious.
Application Example five
For trying disease: downy mildew of garpe
Test medicine provides by Shanxi Thompson Biological Technology Co., Ltd..
Experimental scheme: effective inhibition concentration scope of determining the former medicine of azoles mepanipyrim and Fenamidone and the two different proportioning mixture through preliminary experiment.
The composite toxicity test analysis of results table to downy mildew of garpe of table 13 azoles mepanipyrim and Fenamidone
Figure BDA00002538973600191
As shown in Table 13, azoles mepanipyrim and the Fenamidone proportioning synergy ratio SR to downy mildew of garpe in the time of 1 ︰ 80 ~ 80 ︰ 1 is all greater than 1.5, illustrate that both all show synergistic effect at mixture in 1 ︰ 80 ~ 80 ︰ 1 scopes, when the proportioning of azoles mepanipyrim and Fenamidone is during at 1 ︰ 20 ~ 25 ︰ 1, synergistic effect is more outstanding, and synergy ratio is all more than 2.20.In the time that applicant tests the optimum ratio of finding azoles mepanipyrim and Fenamidone and is 25:1,20:1,15:1,10:1,8:1,7:1,6:1,5:1,4:1,3:1,2:1,1:1,1:2,1:3,1:4,1:5,1:6,1:8,1:10,1:12,1:15,1:20, especially synergy ratio maximum in the time that azoles mepanipyrim and Fenamidone weight ratio are 2:1, synergistic effect is the most obvious.
Application Example six
For trying disease: tomato blight
Test medicine provides by Shanxi Thompson Biological Technology Co., Ltd..
Experimental scheme: effective inhibition concentration scope of determining azoles mepanipyrim and carbendazim active compound and the two different proportioning mixture through preliminary experiment.
The composite toxicity test analysis of results table to tomato blight of table 14 azoles mepanipyrim and carbendazim
Figure BDA00002538973600201
As shown in Table 14, azoles mepanipyrim and the carbendazim proportioning synergy ratio SR to tomato blight in the time of 1 ︰ 80 ~ 80 ︰ 1 is all greater than 1.5, illustrate that both all show synergistic effect at mixture in 1 ︰ 80 ~ 80 ︰ 1 scopes, when the proportioning of azoles mepanipyrim and carbendazim is during at 1 ︰ 30 ~ 25 ︰ 1, synergistic effect is more outstanding, and synergy ratio is all more than 2.25.Test and find that the optimum ratio of azoles mepanipyrim and carbendazim is 25:1,20:1,15:1,10:1,8:1,6:1,4:1,3:1,2:1,1:1,1:2,1:3,1:4,1:5,1:6,1:7,1:8,1:10,1:15,1:20,1:25,1:30 through applicant, especially synergy ratio maximum in the time that azoles mepanipyrim and carbendazim weight ratio are 1:3, synergistic effect is the most obvious.
Application Example seven
For trying disease: rice blast
Test medicine provides by Shanxi Thompson Biological Technology Co., Ltd..
Experimental scheme: effective inhibition concentration scope of determining azoles mepanipyrim and Prochloraz or the former medicine of its salt and the two different proportioning mixture through preliminary experiment.
The composite toxicity test analysis of results table to rice blast of table 15 azoles mepanipyrim and Prochloraz or its salt
Figure BDA00002538973600211
As shown in Table 15, azoles mepanipyrim and Prochloraz or its salt proportioning synergy ratio SR to rice blast in the time of 1 ︰ 80 ~ 80 ︰ 1 is all greater than 1.5, illustrate that both all show synergistic effect at mixture in 1 ︰ 80 ~ 80 ︰ 1 scopes, when the proportioning of azoles mepanipyrim and Prochloraz or its salt is during at 1 ︰ 30 ~ 30 ︰ 1, synergistic effect is more outstanding, and synergy ratio is all more than 2.15.Test and find that the optimum ratio of azoles mepanipyrim and Prochloraz or its salt is 30:1,20:1,15:1,10:1,6:1,5:1,4:1,3:1,2:1,1:1,1:2,1:3,1:4,1:5,1:6,1:10,1:13,1:15,1:20,1:25,1:30 through applicant, especially synergy ratio maximum in the time that azoles mepanipyrim and Prochloraz or its salt weight ratio are 1:1, synergistic effect is the most obvious.
Find through test: after azoles mepanipyrim and active component B are composite, the control of the downy mildew in various crop, epidemic disease, scab, powdery mildew, anthracnose, peronospora tabacina, head blight, damping off, spot defoliation, rice blast, brown spot, stalk break, leaf mold, leaf rot, banded sclerotial blight, shot hole, rust, green mould or penicilliosis is had to obvious synergistic effect, synergy ratio SR is all greater than 1.5.
Effect experiment part: test medicine is researched and developed, provided by Shanxi Thompson Biological Technology Co., Ltd., contrast medicament 20% azoles mepanipyrim suspending agent (autogamy), 70% thiophanate-methyl wetting powder (commercial), 100 grams per liter cyazofamid suspending agents (commercial), 30% triflumizole wettable powder (commercial), 50% Fenamidone suspending agent (autogamy), 25% carbendazol wettable powder (commercial), 25% Prochloraz missible oil (commercial).
Application Example eight azoles mepanipyrims and thiophanate-methyl or fluorine bacterium azoles and the composite powdery mildew of cucumber test of pesticide effectiveness of preventing and treating thereof.
This test arrangement is at Xian District, Shanxi Province suburban area, and investigation powdery mildew of cucumber disease index before medicine, in the dispenser of disease initial stage of origination, investigates disease indexes and calculate preventive effect for after dispenser 3 days, 10 days, 20 days.Result of the test is as follows:
Table 16 azoles mepanipyrim and thiophanate-methyl or fluorine bacterium azoles and the composite powdery mildew of cucumber test of pesticide effectiveness of preventing and treating thereof
Figure BDA00002538973600231
As can be seen from Table 16, after azoles mepanipyrim and thiophanate-methyl or fluorine bacterium azoles are composite, can effectively prevent and treat powdery mildew of cucumber, test and find that azoles mepanipyrim and thiophanate-methyl or fluorine bacterium azoles also can effectively prevent and treat cucumber downy mildew, anthracnose, epidemic disease, stalk break, damping off after composite through applicant, control efficiency is all higher than 96%, be better than the preventive effect of single dose, and the preventive effect phase is long.In test scope of medication, target crop is had no adverse effects.
Application Example nine azoles mepanipyrims and cyazofamid or Fenamidone or carbendazim and the composite control cucumber downy mildew test of pesticide effectiveness thereof.
This test arrangement is at Xian District, Shanxi Province suburban area, and investigation cucumber downy mildew disease index before medicine, in the dispenser of disease initial stage of origination, investigates disease indexes and calculate preventive effect for after dispenser 5 days, 15 days, 30 days.Result of the test is as follows:
Table 17 azoles mepanipyrim and cyazofamid or Fenamidone or carbendazim and the composite control cucumber downy mildew test of pesticide effectiveness thereof
Figure BDA00002538973600241
As can be seen from Table 17, after azoles mepanipyrim and cyazofamid or Fenamidone or carbendazim are composite, can effectively prevent and treat cucumber downy mildew, test and find that azoles mepanipyrim and cyazofamid or Fenamidone or carbendazim also can effectively prevent and treat powdery mildew of cucumber, epidemic disease after composite through applicant, control efficiency is all higher than 95%, be better than the preventive effect of single dose, and the preventive effect phase is long.In test scope of medication, target crop is had no adverse effects.
Application Example ten azoles mepanipyrims and Prochloraz or its salt and the composite control rice blast test of pesticide effectiveness thereof.
This test arrangement is in Hanzhong City suburb, Shaanxi Province, and investigation rice blast disease index before medicine, in the dispenser of disease initial stage of origination, investigates disease indexes and calculate preventive effect for after dispenser 5 days, 15 days, 30 days.Result of the test is as follows:
Table 18 azoles mepanipyrim and Prochloraz or its salt and the composite control rice blast test of pesticide effectiveness thereof
Figure BDA00002538973600251
As can be seen from Table 18, azoles mepanipyrim and Prochloraz or its salt and composite control rice blast thereof, test and find that azoles mepanipyrim and Prochloraz or its salt also can effectively prevent and treat rice sheath blight disease after composite through applicant, and control efficiency is all higher than 95%, be better than the preventive effect of single dose, and the preventive effect phase is long.In test scope of medication, target crop is had no adverse effects.
Application Example 11 azoles mepanipyrims and active component B and the composite control alternaria leaf spot of apple test of pesticide effectiveness thereof.
This test arrangement is at Shaanxi Province's Weinan City Baishui County, and investigation alternaria leaf spot of apple disease index before medicine, in the dispenser of disease initial stage of origination, investigates disease indexes and calculate preventive effect for after dispenser 3 days, 10 days, 20 days.Result of the test is as follows:
Table 19 azoles mepanipyrim and active component B and the composite control alternaria leaf spot of apple test of pesticide effectiveness thereof
Figure BDA00002538973600261
As can be seen from Table 19, after azoles mepanipyrim and active component B are composite, can effectively prevent and treat alternaria leaf spot of apple, test and find that azoles mepanipyrim and active component B also can effectively prevent and treat apple scab, rust, brown spot, anthracnose after composite through applicant, control efficiency is all higher than 96%, be better than the preventive effect of single dose, and the preventive effect phase is long.In test scope of medication, target crop is had no adverse effects.
Application Example ten diazole mepanipyrims and cyazofamid or Fenamidone or carbendazim and the composite control litchi peronospora tabacina test of pesticide effectiveness thereof.
This test arrangement is in suburb, Huilai county, Jie Yang County Guangdong Provice, and before medicine, investigation litchi peronospora tabacina disease index, in the dispenser of disease initial stage of origination, investigates disease indexes and calculate preventive effect for after dispenser 10 days, 20 days, 30 days.Result of the test is as follows:
Table 20 azoles mepanipyrim and cyazofamid or Fenamidone or carbendazim and the composite control litchi peronospora tabacina test of pesticide effectiveness thereof
As can be seen from Table 20, after azoles mepanipyrim and cyazofamid or Fenamidone or carbendazim are composite, can effectively prevent and treat litchi peronospora tabacina, test and find that azoles mepanipyrim and cyazofamid or Fenamidone or carbendazim also can effectively prevent and treat litchi downy mildew, anthracnose after composite through applicant, control efficiency is all higher than 96%, be better than the preventive effect of single dose, and the preventive effect phase is long.In test scope of medication, target crop is had no adverse effects.
Application Example ten triazole mepanipyrims and cyazofamid or Fenamidone or carbendazim and the composite downy mildew of garpe test of pesticide effectiveness of preventing and treating thereof.
This test arrangement is in Weinan City Dali County, Shaanxi Province, and investigation downy mildew of garpe disease index before medicine, in the dispenser of disease initial stage of origination, investigates disease indexes and calculate preventive effect for after dispenser 7 days, 14 days, 25 days.Result of the test is as follows:
Table 21 azoles mepanipyrim and cyazofamid or Fenamidone or carbendazim and the composite downy mildew of garpe test of pesticide effectiveness of preventing and treating thereof
Figure BDA00002538973600281
As can be seen from Table 21, after azoles mepanipyrim and cyazofamid or Fenamidone or carbendazim are composite, can effectively prevent and treat downy mildew of garpe, test and find that azoles mepanipyrim and cyazofamid or Fenamidone or carbendazim also can effectively prevent and treat grape powdery mildew after composite through applicant, control efficiency is all higher than 95%, be better than the preventive effect of single dose, and the preventive effect phase is long.In test scope of medication, target crop is had no adverse effects.
After draw through different local throughout the country tests, azoles mepanipyrim and thiophanate-methyl, cyazofamid, fluorine bacterium azoles, Fenamidone, carbendazim, Prochloraz or its salt composite rear to the preventive effect of the Common Diseases such as the downy mildew in various crop, epidemic disease, scab, powdery mildew, anthracnose, peronospora tabacina, head blight, damping off, spot defoliation, rice blast, brown spot, stalk break, leaf mold, leaf rot, banded sclerotial blight, shot hole, rust, green mould or penicilliosis all more than 95%, be better than single dose preventive effect, synergistic effect is obvious.

Claims (6)

1. the bactericidal composition containing azoles mepanipyrim, effective active composition is active components A and active component B, it is characterized in that: active components A and active component B weight ratio are 1 ︰ 80 ~ 80 ︰ 1, described active components A is selected from azoles mepanipyrim, and active component B is selected from the one in thiophanate-methyl, cyazofamid, fluorine bacterium azoles, Fenamidone, carbendazim, Prochloraz or its salt.
2. the bactericidal composition containing azoles mepanipyrim according to claim 1, is characterized in that: the weight ratio of active components A and active component B is 1 ︰ 50 ~ 50 ︰ 1.
3. the bactericidal composition containing azoles mepanipyrim according to claim 2, is characterized in that:
The weight ratio of azoles mepanipyrim and thiophanate-methyl is 1 ︰ 25 ~ 20 ︰ 1;
The weight ratio of azoles mepanipyrim and cyazofamid or Fenamidone is 1 ︰ 20 ~ 25 ︰ 1;
The weight ratio of azoles mepanipyrim and fluorine bacterium azoles is 1 ︰ 25 ~ 30 ︰ 1;
The weight ratio of azoles mepanipyrim and carbendazim is 1 ︰ 30 ~ 25 ︰ 1;
The weight ratio of azoles mepanipyrim and Prochloraz or its salt is 1 ︰ 30 ~ 30 ︰ 1.
4. according to the bactericidal composition containing azoles mepanipyrim described in any one in claims 1 to 3, it is characterized in that: composition is made wetting powder, water dispersible granules, suspending agent, suspension emulsion, aqueous emulsion, microemulsion, microcapsule suspending agent or microcapsule suspension-suspending agent.
5. the bactericidal composition containing azoles mepanipyrim according to claim 4 is for preventing and treating the purposes of disease on crops.
6. purposes according to claim 5, it is characterized in that, described disease comprises: downy mildew, epidemic disease, scab, powdery mildew, anthracnose, peronospora tabacina, head blight, damping off, spot defoliation, rice blast, brown spot, stalk break, leaf mold, leaf rot, banded sclerotial blight, shot hole, rust, green mould or penicilliosis.
CN201210521269.5A 2012-12-06 2012-12-06 Fungicidal composition containing ametoctradin Pending CN103843804A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210521269.5A CN103843804A (en) 2012-12-06 2012-12-06 Fungicidal composition containing ametoctradin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210521269.5A CN103843804A (en) 2012-12-06 2012-12-06 Fungicidal composition containing ametoctradin

Publications (1)

Publication Number Publication Date
CN103843804A true CN103843804A (en) 2014-06-11

Family

ID=50852262

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201210521269.5A Pending CN103843804A (en) 2012-12-06 2012-12-06 Fungicidal composition containing ametoctradin

Country Status (1)

Country Link
CN (1) CN103843804A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011108759A2 (en) * 2010-03-03 2011-09-09 Sumitomo Chemical Company, Limited Plant disease controlling composition and method for controlling plant disease
WO2011131602A2 (en) * 2010-04-20 2011-10-27 Basf Se Fungicidal mixtures based on azolopyrimmidinylamines
CN102318622A (en) * 2005-07-27 2012-01-18 巴斯夫欧洲公司 Fungicidal mixture based on azoles and pyrimidine radicals amine

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102318622A (en) * 2005-07-27 2012-01-18 巴斯夫欧洲公司 Fungicidal mixture based on azoles and pyrimidine radicals amine
WO2011108759A2 (en) * 2010-03-03 2011-09-09 Sumitomo Chemical Company, Limited Plant disease controlling composition and method for controlling plant disease
WO2011131602A2 (en) * 2010-04-20 2011-10-27 Basf Se Fungicidal mixtures based on azolopyrimmidinylamines

Similar Documents

Publication Publication Date Title
CN104336033A (en) A compound sterilization composition containing oxathiapiprolin and thiocarbamate
CN103651451A (en) Pesticide composition containing penthiopyrad
CN104012541A (en) Fungicidal composition containing diflumetorim and triazole
CN103563960A (en) Fungicidal composition
CN103651460B (en) Pesticide composition containing fluorine azole activated ester and methoxy acrylic esters
CN103518741A (en) Fluopyram-containing high-efficiency bactericidal composition
CN103875696B (en) A kind of bactericidal composition containing amine benzene pyrrole bacterium ketone
CN103828821B (en) A kind of bactericidal composition containing azoles mepanipyrim and methoxy acrylic
CN104412983A (en) Efficient bactericidal composition containing fluoride ether bacteria amide
CN103535362A (en) Efficient bactericidal composition
CN103891739A (en) Sterilization composition containing initium and amides
CN103621562A (en) Bactericidal composition
CN103704229A (en) Bactericidal composition containing fluorine azole activated ester
CN103621550A (en) Chesulfamide-containing pesticide composition
CN103583562A (en) An efficient sterilization composition containing hexamethylene flusulfamide
CN103651417A (en) Bactericidal composition containing zoxamide and methoxyacrylate
CN103583534B (en) Efficient pesticide composition containing cyclohexyl flusulfamide
CN103651414A (en) Fungicidal composition containing fluoro-azole acibenzolar and methoxyl acrylate
CN104026142A (en) Pesticide composition containing fenpyrazamine and strobilurin
CN103843804A (en) Fungicidal composition containing ametoctradin
CN104012556A (en) Microbicide composition containing diflumetorim and thiocarbamate
CN103563935B (en) A kind of bactericidal composition containing bromuconazole and aminodithioformic acid lipid
CN103621527A (en) Sterilization composition containing cyclohexyl flusulfamide
CN103858884A (en) Sterilization composition containing metrafenone and methoxy acrylate
CN104106582A (en) Bactericidal composition containing triclopyricarb and thiocarbamate

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20140611