CN106259350A - A kind of bactericidal composition containing Fenamidone - Google Patents
A kind of bactericidal composition containing Fenamidone Download PDFInfo
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- CN106259350A CN106259350A CN201610653143.1A CN201610653143A CN106259350A CN 106259350 A CN106259350 A CN 106259350A CN 201610653143 A CN201610653143 A CN 201610653143A CN 106259350 A CN106259350 A CN 106259350A
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group, wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, 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
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
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Abstract
The invention discloses a kind of bactericidal composition containing Fenamidone, bactericidal composition containing active components A Yu active component B, active components A is selected from Fenamidone, active component B is selected from any one compound following: mandipropamid, fluopicolide, zoxamide, fluopyram, fluxapyroxad, and the weight ratio of active components A and active component B is 1 70～70 1.The present composition has greater activity to the multiple diseases in various crop, and has obvious potentiation, expands fungicidal spectrum.And have that dosage is little, resistance of rainwater washing against, the obvious feature of potentiation.
Description
The application is divisional application, and original application is patent application " a kind of bacterium Han imidazoles of Shaanxi Meibang Pesticide Co., Ltd.
The bactericidal composition of ketone ", the Application No. 201210199142.6 of original application, original application day is 2012.6.16.
Technical field
The invention belongs to technical field of pesticide, relate to a kind of bactericidal composition containing Fenamidone answering in crop pest
With.
Technical background
Fenamidone (fenamidone) molecular formula: C17H17N3OS, chemical name: (S)-1-anilino--4-methyl-2-first
Sulfenyl-4-benzylimidazoline-5-ketone, Fenamidone and Famoxate and the mechanism of action of methoxy acrylic bactericide
It is similar, suppresses line runic to exhale by stating blocks electrons transfer in former side of body level at hydrogenation olive ferment Q mono-cytochrome C radon
Inhaling, imidazoles bacterium cave (S)-enantiomer specific activity (R)-enantiomer is much higher.
Mandipropamid (mandipropamid) chemical name: 2-(the chloro-phenyl of 4-)-N-[2-(3-methoxyl group-4-(2-
Propargyl alcoholate)-phenyl)-ethyl group]-2-(2-propargyl alcoholate)-with amide, molecular formula: C23H22ClNO4, belong to CAA series bactericidal agent,
The overwhelming majority there is good preventive effect by the microbial leaf diseases of Oomycete cause of disease.The spore being in the sprouting stage had pole
High activity, may also suppress the formation of mycelial growth and spore in addition.Stronger treatment is had to being in preclinical plant disease
Effect.Owing to the wax coat of leaf table has good affinity to this medicine, so this preparation has extraordinary lasting effect.
The chloro-N-of fluopicolide (fluopicolide) chemical name: 2,6-bis-[(3-chloro-5-trifluoromethyl-2-pyridine radicals)
Methyl] Benzoylamide, molecular formula: C14H8Cl3F3N2O, this medicine protectiveness is good, permeability strong, and guiding principle fungus diseases true to oomycetes has higher
Biological activity, there is good prevention effect.Can conduct from leaves of plants basal orientation blade tip direction.
The mechanism of action of zoxamide is unique in Oomycete antibacterial, zoxamide do not affect travelling spore in
Travelling, sporangiocyst is formed or sprouts.Along with caryocinetic first circulation of bacterium, the elongation of germ tube is suppressed, thus stops disease
Bacterium penetrates host plant.
Fluopyram (fluopyram) chemical name: N-{2-[3-chloro-5-(trifluoromethyl)-2-pyridine radicals) ethyl]-
α, α, α-three fluoro-0-toluamide, molecular formula: C16H11ClF6N2O.Fluopyram is by hindering succinic acid dehydrogenation in respiratory chain
The electron transfer of enzyme and suppress mitochondrial respiratory.Reached by the several stages in the suppression growth of pathogenic bacteria cycle to control to cause a disease
The purpose of bacterium, is mainly used on broad leaf crop preventing and treating the microbial disease of ascus.
Fluxapyroxad (Fluxapyroxad) chemical name: 3-(difluoro)-1-methyl-N-(3', 4', 5'-trifluoro [1,
1'-biphenyl]-2-base)-1-H-pyrazoles-4-amide, fluxapyroxad belongs to pyrazole amide series bactericidal agent, and succinate dehydrogenase suppresses
Agent, is integrated in one superior lasting effect with lasting transmission characteristic.
In the real process of agricultural production, controlling disease is easiest to generate the problem that the generation of disease drug resistance.No
Compound with kind composition, be to prevent and treat the method that resistance disease is the most common.Heterogeneity compounds, according to reality application effect
Really, judge certain compounding be potentiation, add and or antagonism.In most cases, the compounding effect of pesticide all adds
And effect, really have potentiation compounding seldom, especially potentiation clearly, potentiation ratio the highest compounding the most more
Few.Study through inventor, find by Fenamidone and mandipropamid, fluopicolide, zoxamide, fluopyram,
Fluxapyroxad is the most compounding, has good potentiation within the specific limits, and about Fenamidone and mandipropamid, fluorine
Pyrrole bacterium amine, zoxamide, fluopyram, the relevant of fluxapyroxad compound, and the most at home and abroad there is not yet relevant report.
Summary of the invention
The purpose of the present invention is to propose to a kind of have that synergistic function, use cost be low, preventive effect is good containing Fenamidone
Bactericidal composition.
The present invention is to be achieved through the following technical solutions:
A kind of bactericidal composition containing Fenamidone, containing active components A and active component B, active components A becomes with activity
Dividing B weight ratio is 1 70～70 1, and described active components A is selected from Fenamidone, and active component B is selected from mandipropamid, fluorine
One of pyrrole bacterium amine, zoxamide, fluopyram, fluxapyroxad are planted, active components A and the preferred weight of active component B
Ratio is 1 50～50 1；More preferably Fenamidone is 1 30～30 1 with the weight ratio of mandipropamid；Fenamidone and fluorine
The weight ratio of pyrrole bacterium amine is 1 20～30 1；Fenamidone is 1 30～20 1 with the weight ratio of zoxamide；Fenamidone with
The weight ratio of fluopyram is 1 15～30 1；Fenamidone is 1 30～30 1 with the weight ratio of fluxapyroxad, optimum
The weight ratio electing Fenamidone and mandipropamid as is 1 10～10 1；Fenamidone is 1 10 with the weight ratio of fluopicolide
～15 1；Fenamidone is 1 15～10 1 with the weight ratio of zoxamide；Fenamidone with the weight ratio of fluopyram is
1 5～10 1；Fenamidone is 1 10～10 1 with the weight ratio of fluxapyroxad.
The described bactericidal composition containing Fenamidone is for preventing and treating the application of the disease of crop, and described crop includes grain
Food crop, legume crop, fibre crops, sugar crop, melon crop, fruits crop, dry fruit crop, hobby crop, root
Stem class crop, oil crop, flower crop, medicinal crop, crop, green manure pasture crop.
The described bactericidal composition containing Fenamidone is for preventing and treating the application of the disease of crop, and described disease includes frost
Mildew, late blight, early blight, melasma, mottled rot disease, damping off, epidemic disease, rice blast, gray mold, powdery mildew, moire disease, filigree
Disease, leaf spot, leaf blight, banded sclerotial blight, scab, phytophthora root rot, damping-off.
In the present composition, the content of active component depends on amount of application when being used alone, and also depends on a kind of chemical combination
The mixed ratio of thing and another kind of compound and potentiation degree, also the most relevant with target disease.Generally in compositions
The weight percentage of active component is the 1%～90% of gross weight, is preferably 5%～80%.According to different preparation classes
Type, active component content scope is different.Generally, liquid preparation contains the active substance of by weight 1%～60%, preferably
Ground is 5%～50%；Solid preparation contains the active substance of by weight 5%～80%, preferably 10%～80%.
At least containing a kind of surfactant in the bactericidal composition of the present invention, when being beneficial to use, active component is in water
Dispersion.Surface-active contents is the 2%～30% of total formulation weight amount, and surplus is solid or liquid diluent.
Surfactant selected by the bactericidal composition of the present invention is known in those skilled in the art: can be selected from
One or more in dispersant, wetting agent, thickening agent or defoamer.According to different dosage form, preparation can also contain this area
Stabilizer well known to technical staff, antifreeze etc..
The bactericidal composition of the present invention through dilution or directly can be used before use by user.Its preparation can be by ability
Prepared by the processing method well known to field technique personnel, will add after active component mixes with liquid flux or solid carrier
One or more in surfactant such as dispersant, stabilizer, wetting agent, binding agent, defoamer etc..
The bactericidal composition of the present invention, can be processed into acceptable dosage form on any pesticide on demand.Wherein preferably agent
Type is wettable powder, water dispersible granules, suspending agent, suspension emulsion, microemulsion, aqueous emulsion, microcapsule suspending agent, microcapsule suspension-outstanding
Floating agent.
Compositions comprises following component and content when making wettable powder: active components A 1%～70%, active component B
1%～70%, dispersant 1%～12%, wetting agent 1%～8%, filler surplus.
Compositions includes following component and content when making water dispersible granules: active components A 1%～70%, active component B
1%～70%, more than dispersant 1%～12%, wetting agent 1%～8%, disintegrating agent 1%～10%, binding agent 0～8%, filler
Amount.
Compositions includes following component and content when making suspending agent: active components A 1%～50%, active component B1%
～50%, dispersant 1%～10%, wetting agent 1%～10%, defoamer 0.01%～2%, thickening agent 0～2%, antifreeze 0
～8%, deionized water add to 100%.
Compositions includes following component and content when making suspension emulsion: active components A 1%～50%, active component B1%
～50%, emulsifying agent 1%～10%, dispersant 1%～10%, solvent 1%～20%, defoamer 0.01%～2%, thickening agent
0～2%, antifreeze 0～8%, deionized water add to 100%.
Compositions includes following component and content when making microemulsion: active components A 1%～50%, active component B1%
～50%, emulsifying agent 3%～25%, solvent 1%～10%, antifreeze 0～8%, defoamer 0.01%～2%, deionized water
Add to 100%.
Compositions includes following component and content when making aqueous emulsion: active components A 1%～50%, active component B 1%
～50%, solvent 1%～20%, emulsifying agent 1%～12%, antifreeze 0～8%, defoamer 0.01%～2%, thickening agent 0～
2%, deionized water adds to 100%.
Compositions includes following component and content when making microcapsule suspending agent: active components A 1%～50%, active component
B1%～50%, macromolecule cyst material 1%～10%, dispersant 2%～10%, solvent 1%～10%, emulsifying agent 1%～
7%, pH adjusting agent 0.01%～5%, defoamer 0.01%～2%, deionized water add to 100%.
Compositions includes following component and content when making microcapsule suspension-suspendinagent agent: active components A 1%～50%, activity
Composition B1%～50%, macromolecule cyst material 1%～12%, dispersant 1%-12%, wetting agent 1%-8%, solvent 1%～
15%, emulsifying agent 1%～8%, defoamer 0.01%～2%, thickening agent 0～2%, pH adjusting agent 0.01%～5%, deionization
Water adds to 100%.
The wettable powder the key technical indexes of the present invention:
The water dispersible granules the key technical indexes of the present invention:
The suspending agent the key technical indexes of the present invention:
The suspension emulsion the key technical indexes of the present invention:
The microemulsion the key technical indexes of the present invention:
The aqueous emulsion the key technical indexes of the present invention:
It is an advantage of the current invention that:
(1) present composition has good potentiation and lasting effect within the specific limits, and preventive effect is higher than single dose；(2) agriculture
Medicinal dose reduces, and reduces pesticide residual quantity on crop, alleviates environmental pollution；(3) fungicidal spectrum is expanded, to multiple diseases
As downy mildew, late blight, early blight, melasma, mottled rot disease, damping off, epidemic disease, rice blast, gray mold, powdery mildew, moire disease,
Net blotch, leaf spot, leaf blight, banded sclerotial blight, scab, phytophthora root rot, damping-off have greater activity.
Detailed description of the invention
Below in conjunction with embodiment, further instruction of the present invention, the percentage ratio in embodiment are all weight percentage, but
The invention is not limited in this.
Application Example one
Embodiment 1～17 wettable powder
By Fenamidone, active component B, dispersant, wetting agent, filler mixing, mix homogeneously in mixed cylinder, through air-flow
Pulverizer remixes uniformly after pulverizing, and i.e. can be made into wettable powder product of the present invention.Specifically it is shown in Table 1.
Table 1 embodiment 1～17 each component and content
Embodiment 18～34 water dispersible granules
By Fenamidone, active component B, dispersant, wetting agent, disintegrating agent, binding agent (can add and can be not added with), filler together
Obtain the particle diameter needed through comminution by gas stream, obtain granulation materials.System is passed through in item is quantitatively sent into fluidized bed granulating dryer
Grain and dried, prepares water dispersible granules product of the present invention.Specifically it is shown in Table 2.
Table 2 embodiment 18～34 each component and content
Embodiment 35～51 suspending agent
By dispersant, wetting agent, thickening agent (can add and can be not added with), defoamer, antifreeze (can add and can be not added with) through at a high speed
Shear-mixed is uniform, adds Fenamidone, active component B, supplies surplus with deionized water, and in ball mill, ball milling 2～3 is little
Time, make diameter of particle all below 5 μm, prepare suspending agent product of the present invention.Specifically it is shown in Table 3.
Table 3 embodiment 35～51 each component and content
Embodiment 52～56 suspension emulsion
By dispersant, defoamer, thickening agent (can add and can be not added with), antifreeze (can add and can be not added with), deionized water through too high
Speed shear-mixed is uniform, adds Fenamidone, ball milling 2～3 hours in ball mill, makes diameter of particle all below 5 μm, system
Obtain Fenamidone suspending agent, then by active component B, solvent (can add and can be not added with), emulsifying agent and various auxiliary agent high-speed stirred
The direct emulsifying of device, in suspending agent, prepares suspension emulsion product of the present invention.Specifically it is shown in Table 4.
Table 4 embodiment 52～56 each component and content
Embodiment 57～68 aqueous emulsion
Fenamidone, active component B, solvent, emulsifying agent are added together, make to be dissolved into homogeneous oil phase；By deionized water,
Antifreeze (can add and can be not added with), thickening agent (can add and can be not added with), defoamer mix, and become homogeneous aqueous phase.In high-speed stirred
Under, aqueous phase is added oil phase, prepares aqueous emulsion product of the present invention.Specifically it is shown in Table 5.
Table 5 example 57～68 each component and content
Mandipropamid, fluopicolide, zoxamide, fluopyram, fluxapyroxad in table 1～5 are exchanged, can make
Obtain novel formulation.
Embodiment 69～71 microemulsion
Being dissolved in Fenamidone, active component B equipped with in the homogenizer of solvent, by emulsifying agent, antifreeze, (can add can not
Add), defoamer join in the homogenizer equipped with above-mentioned solution, strongly mix and even after supplying surplus with deionized water
Change, finally obtain the microemulsion product of the present invention that clear appearance is transparent.Specifically it is shown in Table 6.
Table 6 embodiment 69～71 each component and content
Embodiment 72,73 microcapsule suspending agent
By Fenamidone, active component B, macromolecule cyst material, solvent mixing, make to be dissolved into homogeneous oil phase, shearing
Under the conditions of, oil phase is joined containing emulsifying agent, pH adjusting agent, dispersant, defoamer aqueous phase solution in, mend with deionized water
Foot surplus, bi-material reacts at oil-water interfaces, forms macromolecule cyst wall, makes the present composition finely disseminated micro-
Capsule suspending agent product.Specifically it is shown in Table 7.
Table 7 embodiment 72,73 each component and content
Embodiment 74,75 microcapsule suspension-suspendinagent agent
By active component B, macromolecule cyst material, solvent mixing, make to be dissolved into homogeneous oil phase, by oil phase at shearing condition
Under join containing emulsifying agent, pH adjusting agent aqueous phase solution in, make finely disseminated microcapsule suspending agent.By dispersant, wet
Profit agent, defoamer, thickening agent (can add and can be not added with), through high speed shear mix homogeneously, add Fenamidone, ball in ball mill
Grind 2～3 hours, make diameter of particle all below 5 μm, prepare suspending agent, then suspending agent is joined micro-capsule suspension
Aqueous phase solution in, deionized water supplies surplus, makes the present composition finely disseminated microcapsule suspension-suspendinagent agent product.
Specifically it is shown in Table 8.
Table 8 embodiment 74,75 each component and content
The embodiment of the present invention is the method using Toxicity Determination and field test to combine.First pass through indoor virulence to survey
Fixed, after clear and definite two kinds of medicaments are compounding by a certain percentage potentiation ratio (SR), SR ＜ 0.5 is antagonism, 0.5≤SR≤1.5
For summation action, SR ＞ 1.5 is potentiation, on this basis, then carries out field test.
Test method: after prerun determines each medicament effective inhibition concentration scope, medicament is set 5 respectively by active constituent content
Individual dosage processes, if clear water comparison.Carry out with reference to " farm-chemical indoor determination test rule antibacterial ", use mycelial growth speed
Rate method measures the medicament virulence to crop pathogenic bacteria.Measure colony diameter by decussation method after 72h, calculate each process and only grow
Amount, mycelial growth inhibition rate.
Net growth (mm)=measurement colony diameter-5
Mycelial growth inhibition rate is converted into probit value (y), and liquor strength (μ g/mL) is converted into logarithm value (x), with minimum
Square law tries to achieve virulence regression equation (y=a+bx), and thus calculates the EC of every kind of medicament50Value.Simultaneously according to Wadley method
Calculating two medicaments different ratio synergy ratio (SR), SR ＜ 0.5 is antagonism, and 0.5≤SR≤1.5 are summation action,
SR ＞ 1.5 is potentiation.Computing formula is as follows:
Wherein: a, b are respectively the ratio that active components A is shared in combination with active component B；A is Fenamidone；B selects
Plant to one of mandipropamid, fluopicolide, zoxamide, fluopyram, fluxapyroxad.
Application Example two:
For examination disease: the late blight of potato；Test medicine is provided by Shaanxi Meibang Pesticide Co., Ltd.；EXPERIMENTAL DESIGN:
Fenamidone and the former medicine of mandipropamid and effective inhibition concentration scope of the two different ratio mixture is determined through pilot study.
Toxicity test result
Table 9 Fenamidone toxicity test analysis of results table to the late blight of potato compounding with mandipropamid
As shown in Table 9, Fenamidone and mandipropamid compound the proportioning preventing and treating the late blight of potato 1 70～70 1
Time, potentiation ratio SR is all higher than 1.5, illustrates that both all show potentiation at mixture in the range of 1 70～70 1, works as imidazoles
The proportioning of bacterium ketone and mandipropamid is when 1 30～30 1, and potentiation is the most prominent, and potentiation ratio is all higher than 2.15.Through examination
The optimum ratio issuing after examination and approval existing Fenamidone and mandipropamid is 30:1,25:1,20:1,15:1,10:1,9:1,8:1,7:1,6:
1,5:1,1:1,1:2,1:3,1:4,1:5,1:6,1:7,1:8,1:9,1:10,1:11,1:12,1:13,1:14,1:15,1:20,
1:25,1:30, especially when Fenamidone and mandipropamid weight ratio are 1:1, potentiation ratio is maximum, and potentiation is the most
Substantially.
Application Example three:
For examination disease: cucumber downy mildew；Test medicine is provided by Shaanxi Meibang Pesticide Co., Ltd.；EXPERIMENTAL DESIGN: warp
Cross pilot study and determine Fenamidone and the former medicine of fluopicolide and effective inhibition concentration scope of the two different ratio mixture.
Toxicity test result
Table 10 Fenamidone toxicity test analysis of results table to cucumber downy mildew compounding with fluopicolide
As shown in Table 10, Fenamidone and fluopicolide compound the proportioning of preventing and treating cucumber downy mildew when 1 70～70 1,
Potentiation ratio SR is all higher than 1.5, illustrates that both all show potentiation at mixture in the range of 1 70～70 1, works as Fenamidone
With the proportioning of fluopicolide when 1 20～30 1, potentiation is the most prominent, and potentiation ratio is all higher than 2.10.Find through test
The optimum ratio of Fenamidone and fluopicolide is 30:1,25:1,20:1,15:1,10:1,9:1,8:1,7:1,6:1,5:1,1:
1,1:2,1:3,1:4,1:5,1:6,1:7,1:8,1:9,1:10,1:11,1:12,1:13,1:14,1:15,1:20, especially when
When Fenamidone and fluopicolide weight ratio are 3:2, potentiation ratio is maximum, and potentiation is the most obvious.
Application Example four:
For examination disease: downy mildew of garpe；Test medicine is provided by Shaanxi Meibang Pesticide Co., Ltd.；EXPERIMENTAL DESIGN: warp
Cross pilot study and determine Fenamidone and the former medicine of zoxamide and effective inhibition concentration scope of the two different ratio mixture.
Toxicity test result
Table 11 Fenamidone toxicity test analysis of results table to downy mildew of garpe compounding with zoxamide
As shown in Table 11, Fenamidone and zoxamide compound the proportioning preventing and treating downy mildew of garpe when 1 70～70 1,
Potentiation ratio SR is all higher than 1.5, illustrates that both all show potentiation at mixture in the range of 1 70～70 1, works as Fenamidone
With the proportioning of zoxamide when 1 30～20 1, potentiation is the most prominent, and potentiation ratio is all higher than 2.10.Find through test
The optimum ratio of Fenamidone and zoxamide is 20:1,15:1,10:1,9:1,8:1,7:1,6:1,5:1,1:1,1:2,1:3,
1:4,1:5,1:6,1:7,1:8,1:9,1:10,1:11,1:12,1:13,1:14,1:15,1:20,1:25,1:30, especially when
When Fenamidone and zoxamide weight ratio are 2:3, potentiation ratio is maximum, and potentiation is the most obvious.
Application Example five:
For examination disease: powdery mildew of cucumber；Test medicine is provided by Shaanxi Meibang Pesticide Co., Ltd.；EXPERIMENTAL DESIGN: warp
Cross pilot study and determine Fenamidone and the former medicine of fluopyram and effective inhibition concentration scope of the two different ratio mixture.
Toxicity test result
Table 12 Fenamidone toxicity test analysis of results table to powdery mildew of cucumber compounding with fluopyram
As shown in Table 12, Fenamidone and fluopyram compound the proportioning preventing and treating powdery mildew of cucumber 1 70～70 1
Time, potentiation ratio SR is all higher than 1.5, illustrates that both all show potentiation at mixture in the range of 1 70～70 1, works as imidazoles
The proportioning of bacterium ketone and fluopyram is when 1 15～30 1, and potentiation is the most prominent, and potentiation ratio is all higher than 2.20.Through examination
The optimum ratio issuing after examination and approval existing Fenamidone and fluopyram is 30:1,25:1,20:1,15:1,10:1,9:1,8:1,7:1,6:
1,5:1,1:1,1:2,1:3,1:4,1:5,1:6,1:7,1:8,1:9,1:10,1:11,1:12,1:13,1:14,1:15, especially
Being that potentiation ratio is maximum when Fenamidone and fluopyram weight ratio are 2:1, potentiation is the most obvious.
Application Example six:
For examination disease: wheat sharp eyespot；Test medicine is provided by Shaanxi Meibang Pesticide Co., Ltd.；EXPERIMENTAL DESIGN: warp
Cross pilot study and determine Fenamidone and the former medicine of fluxapyroxad and effective inhibition concentration scope of the two different ratio mixture.
Toxicity test result
Table 13 Fenamidone toxicity test analysis of results table to wheat sharp eyespot compounding with fluxapyroxad
As shown in Table 13, Fenamidone and fluxapyroxad compound the proportioning of preventing and treating wheat sharp eyespot 1 70～70 1
Time, potentiation ratio SR is all higher than 1.5, illustrates that both all show potentiation at mixture in the range of 1 70～70 1, works as imidazoles
The proportioning of bacterium ketone and fluxapyroxad is when 1 30～30 1, and potentiation is the most prominent, and potentiation ratio is all higher than 2.20.Through examination
The optimum ratio issuing after examination and approval existing Fenamidone and fluxapyroxad is 30:1,25:1,20:1,15:1,10:1,9:1,8:1,7:1,6:
1,5:1,1:1,1:2,1:3,1:4,1:5,1:6,1:7,1:8,1:9,1:10,1:11,1:12,1:13,1:14,1:15,1:20,
1:25,1:30, especially when Fenamidone and fluxapyroxad weight ratio are 1:1, potentiation ratio is maximum, and potentiation is the most
Substantially.
Find through test: to downy mildew, late blight, early blight, melasma, speckle after Fenamidone is compounding with active component B
Maize ear rot, damping off, epidemic disease, rice blast, gray mold, powdery mildew, moire disease, net blotch, leaf spot, leaf blight, banded sclerotial blight, black star
Disease, phytophthora root rot, the preventing and treating of damping-off have obvious potentiation, and potentiation ratio is all more than 1.50.
Test of pesticide effectiveness part
Test medicine is researched and developed by Shaanxi Meibang Pesticide Co., Ltd., is provided.Comparison medicament: 20% Fenamidone suspending agent
(autogamy), 23.4% mandipropamid suspending agent (commercial), 10% fluopicolide suspending agent (autogamy), 24% zoxamide suspend
Agent (autogamy), 20% fluopyram suspending agent (autogamy), 10% fluxapyroxad suspending agent (autogamy).
Application Example seven Fenamidone and active component B and compounding prevent and treat the late blight of potato test of pesticide effectiveness
This test arrangement, at Xian District, Shanxi Province suburban area, investigates the late blight of potato state of an illness, in the state of an illness initial stage first before medicine
Secondary dispenser, dispenser in every 7 days once, is total to dispenser 2 times.Within after last dispenser 7 days, 14 days, 30 days, investigate disease index respectively and calculate
Preventive effect.Experimental result is as follows:
Table 14 Fenamidone and active component B and compounding prevent and treat the late blight of potato test of pesticide effectiveness
As can be seen from Table 14, the late blight of potato, preventing and treating effect can effectively be prevented and treated after Fenamidone is compounding with active component B
Fruit is superior to 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 eight Fenamidone and active component B and the compounding preventing and treating cucumber downy mildew test of pesticide effectiveness thereof
This test arrangement, in Jingyang County, Shaanxi Province, investigates the cucumber downy mildew state of an illness before medicine, in the dispenser for the first time of state of an illness initial stage,
Dispenser in every 7 days once, is total to dispenser 2 times.Within after last dispenser 7 days, 14 days, 30 days, investigate disease index respectively and calculate preventive effect.Real
Test result as follows:
Table 15 Fenamidone and active component B and the compounding preventing and treating cucumber downy mildew test of pesticide effectiveness thereof
As can be seen from Table 15, cucumber downy mildew, prevention effect can effectively be prevented and treated after Fenamidone is compounding with active component B
It is superior to 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 Fenamidone and active component B and compounding prevent and treat the downy mildew of garpe test of pesticide effectiveness
This test arrangement, in Weinan City suburb, Shaanxi Province, investigates the downy mildew of garpe state of an illness before medicine, in first time at state of an illness initial stage
Dispenser, dispenser in every 7 days once, is total to dispenser 3 times.Within after last dispenser 7 days, 14 days, 30 days, investigate disease index respectively and calculate anti-
Effect.Experimental result is as follows:
Table 16 Fenamidone and active component B and compounding prevent and treat the downy mildew of garpe test of pesticide effectiveness
As can be seen from Table 16, downy mildew of garpe, prevention effect can effectively be prevented and treated after Fenamidone is compounding with active component B
It is superior to 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 Fenamidone and active component B and the compounding preventing and treating litchi peronospora tabacina test of pesticide effectiveness thereof
This test arrangement, in Zengcheng City of Guangdong Province, investigates the litchi peronospora tabacina state of an illness before medicine, in first time at state of an illness initial stage
Dispenser, dispenser in every 7 days once, is total to dispenser 2 times.Within after last dispenser 7 days, 14 days, 30 days, investigate disease index respectively and calculate anti-
Effect.Experimental result is as follows:
Table 17 Fenamidone and active component B and the compounding preventing and treating litchi peronospora tabacina test of pesticide effectiveness thereof
As can be seen from Table 17, litchi peronospora tabacina can effectively be prevented and treated after Fenamidone is compounding with active component B, preventing and treating
Effect is superior to 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 Fenamidone and active component B and the compounding preventing and treating wheat sharp eyespot test of pesticide effectiveness thereof
This test arrangement, at Shaanxi Province's Weinan City, investigates the wheat sharp eyespot state of an illness before medicine, in the dispenser for the first time of state of an illness initial stage,
Dispenser in every 7 days once, is total to dispenser 2 times.Within after last dispenser 7 days, 14 days, 30 days, investigate disease index respectively and calculate preventive effect.Real
Test result as follows:
Table 18 Fenamidone and active component B and the compounding preventing and treating wheat sharp eyespot test of pesticide effectiveness thereof
As can be seen from Table 18, wheat sharp eyespot, prevention effect can effectively be prevented and treated after Fenamidone is compounding with active component B
It is superior to 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 diimidazole bacterium ketone tries with active component B and compounding downy mildew of crucifers drug effect of preventing and treating thereof
Test
This test arrangement, at Xian District, Shanxi Province suburban area, investigates the downy mildew of crucifers state of an illness, at the beginning of the state of an illness before medicine
Phase dispenser for the first time, dispenser in every 7 days once, is total to dispenser 2 times.Within after last dispenser 7 days, 14 days, 30 days, investigate disease index respectively
And calculate preventive effect.Experimental result is as follows:
Table 19 Fenamidone and active component B and compounding prevent and treat the downy mildew of crucifers test of pesticide effectiveness
As can be seen from Table 19, after Fenamidone is compounding with active component B, can effectively prevent and treat downy mildew of crucifers,
Prevention effect is superior to 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 13 Fenamidone and active component B and compounding prevent and treat the powdery mildew of cucumber test of pesticide effectiveness
This test arrangement, in Huilai county, Guangdong Province, investigates the powdery mildew of cucumber state of an illness before medicine, in the dispenser for the first time of state of an illness initial stage,
Dispenser in every 7 days once, is total to dispenser 2 times.Within after last dispenser 7 days, 14 days, 30 days, investigate disease index respectively and calculate preventive effect.Real
Test result as follows:
Table 20 Fenamidone and active component B and compounding prevent and treat the powdery mildew of cucumber test of pesticide effectiveness
As can be seen from Table 20, powdery mildew of cucumber, prevention effect can effectively be prevented and treated after Fenamidone is compounding with active component B
It is superior to 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 tetramisole bacterium ketone and active component B and the compounding preventing and treating Citrullus vulgaris epidemic disease test of pesticide effectiveness thereof
This test arrangement, in Zhouzhi County, Shaanxi Province, investigates the Citrullus vulgaris epidemic disease state of an illness before medicine, in the dispenser for the first time of state of an illness initial stage, often
Dispenser in 7 days once, is total to dispenser 2 times.Within after last dispenser 7 days, 14 days, 30 days, investigate disease index respectively and calculate preventive effect.Experiment
Result is as follows:
Table 21 Fenamidone and active component B and the compounding preventing and treating Citrullus vulgaris epidemic disease test of pesticide effectiveness thereof
As can be seen from Table 21, can effectively prevent and treat Citrullus vulgaris epidemic disease after Fenamidone is compounding with active component B, prevention effect is equal
It is 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 tests different local throughout the country, Fenamidone and mandipropamid, fluopicolide, benzoyl
To the downy mildew in various crop, late blight, early blight, melasma, speckle after bacterium amine, fluopyram, fluxapyroxad are compounding
Maize ear rot, damping off, epidemic disease, rice blast, gray mold, powdery mildew, moire disease, net blotch, leaf spot, leaf blight, banded sclerotial blight, black star
The preventive effect of the Common Diseases such as disease, phytophthora root rot, damping-off, all more than 95%, is better than single dose preventive effect, and potentiation is obvious.
Claims (6)
1. the bactericidal composition containing Fenamidone, it is characterised in that containing active components A and active component B, active components A
Being 1 70～70 1 with active component B weight ratio, described active components A is selected from Fenamidone, and active component B is selected from fluorine pyrrole bacterium
One of amine, zoxamide, fluopyram, fluxapyroxad are planted.
Bactericidal composition containing Fenamidone the most according to claim 1, it is characterised in that: active components A becomes with activity
The weight ratio dividing B is 1 50～50 1.
Bactericidal composition containing Fenamidone the most according to claim 2, it is characterised in that:
Fenamidone is 1 20～30 1 with the weight ratio of fluopicolide；
Fenamidone is 1 30～20 1 with the weight ratio of zoxamide；
Fenamidone is 1 15～30 1 with the weight ratio of fluopyram；
Fenamidone is 1 30～30 1 with the weight ratio of fluxapyroxad.
4. according to the bactericidal composition containing Fenamidone described in any one in claim 1-3, it is characterised in that: compositions
Make wettable powder, water dispersible granules, suspending agent, suspension emulsion, microemulsion, aqueous emulsion, microcapsule suspending agent, microcapsule suspension-outstanding
Floating agent.
Bactericidal composition containing Fenamidone the most according to claim 4, for preventing and treating the application of crop pest.
Application the most according to claim 5, it is characterised in that: described disease include downy mildew, late blight, early blight,
Melasma, mottled rot disease, damping off, epidemic disease, rice blast, gray mold, powdery mildew, moire disease, net blotch, leaf spot, leaf blight, stricture of vagina
Rot, scab, phytophthora root rot, damping-off.
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| CN201610653143.1A CN106259350A (en) | 2012-06-16 | 2012-06-16 | A kind of bactericidal composition containing Fenamidone |
| CN201210199142.6A CN103503873A (en) | 2012-06-16 | 2012-06-16 | Sterilization composition containing fenamidone |
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Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1245396A (en) * | 1997-12-02 | 2000-02-23 | 罗纳-普朗克农业化学公司 | Fungicide composition containing 2-imidazoline-5-one |
| CN1953662A (en) * | 2004-05-13 | 2007-04-25 | 巴斯福股份公司 | Fungicidal mixtures and novel triazolopyrimidines |
| EP2119362A1 (en) * | 2008-05-15 | 2009-11-18 | Bayer CropScience AG | Method for improving the tolerance of crops to chilling temperatures and/or frost |
| WO2010069489A1 (en) * | 2008-12-19 | 2010-06-24 | Bayer Cropscience Ag | Active compound combinations |
| WO2010135324A1 (en) * | 2009-05-18 | 2010-11-25 | Monsanto Technology Llc | Use of glyphosate for disease suppression and yield enhancement in soybean |
| WO2012004293A2 (en) * | 2010-07-08 | 2012-01-12 | Bayer Cropscience Ag | Insecticide and fungicide active ingredient combinations |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2722652B1 (en) * | 1994-07-22 | 1997-12-19 | Rhone Poulenc Agrochimie | FUNGICIDE COMPOSITION COMPRISING A 2-IMIDAZOLINE-5-ONE |
| GB0011944D0 (en) * | 2000-05-17 | 2000-07-05 | Novartis Ag | Organic compounds |
| CL2007003743A1 (en) * | 2006-12-22 | 2008-07-11 | Bayer Cropscience Ag | COMPOSITION THAT INCLUDES FENAMIDONA AND AN INSECTICIDE COMPOUND; AND METHOD TO CONTROL FITOPATOGENOS CULTURES AND INSECTS FACING OR PREVENTIVELY. |
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2012
- 2012-06-16 CN CN201210199142.6A patent/CN103503873A/en active Pending
- 2012-06-16 CN CN201610653143.1A patent/CN106259350A/en active Pending
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1245396A (en) * | 1997-12-02 | 2000-02-23 | 罗纳-普朗克农业化学公司 | Fungicide composition containing 2-imidazoline-5-one |
| CN1953662A (en) * | 2004-05-13 | 2007-04-25 | 巴斯福股份公司 | Fungicidal mixtures and novel triazolopyrimidines |
| EP2119362A1 (en) * | 2008-05-15 | 2009-11-18 | Bayer CropScience AG | Method for improving the tolerance of crops to chilling temperatures and/or frost |
| WO2010069489A1 (en) * | 2008-12-19 | 2010-06-24 | Bayer Cropscience Ag | Active compound combinations |
| WO2010135324A1 (en) * | 2009-05-18 | 2010-11-25 | Monsanto Technology Llc | Use of glyphosate for disease suppression and yield enhancement in soybean |
| WO2012004293A2 (en) * | 2010-07-08 | 2012-01-12 | Bayer Cropscience Ag | Insecticide and fungicide active ingredient combinations |
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| Title |
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| 无: ""Fungicidal compositions for agricultural, anonymously"", 《RESEARCH DISCLOSURE》 * |
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