CN103688938A - Bactericidal composition containing fluopyram and bupirimate - Google Patents
Bactericidal composition containing fluopyram and bupirimate Download PDFInfo
- Publication number
- CN103688938A CN103688938A CN201310685651.4A CN201310685651A CN103688938A CN 103688938 A CN103688938 A CN 103688938A CN 201310685651 A CN201310685651 A CN 201310685651A CN 103688938 A CN103688938 A CN 103688938A
- Authority
- CN
- China
- Prior art keywords
- bupirimate
- acid amides
- pyrrole bacterium
- fluorine pyrrole
- bacterium acid
- 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
Abstract
The invention discloses a bactericidal composition containing fluopyram and bupirimate. The effective components of the bactericidal composition are fluopyram and bupirimate in a binary compounding manner, and the other components are auxiliary components. The mass ratio of the effective components fluopyram to bupirimate in the bactericidal composition is (1-50):(50-1); and the preparation is prepared from the effective components fluopyram and bupirimate in the preparation with the mass part ratio of 1-80% and the rest of the auxiliary components which are permitted to be used and accepted in a pesticide. The dosage form of the bactericidal composition disclosed by the invention is missible oil, a suspending agent, wettable powder, a water dispersible granule, an emulsion in water, a microemulsion, granules, a microcapsule and water aqua. The diseases such as powdery mildew, downy mildew and the like on vegetables and field crops are effectively controlled.
Description
Technical field
The present invention relates to agriculture chemical compounding technical field, particularly relate to a kind of bactericidal composition that contains fluorine pyrrole bacterium acid amides and bupirimate.
Background technology
Fluorine pyrrole bacterium acid amides is a kind of new benzamides series bactericidal agent, and its chemical name is the chloro-5-(trifluoromethyl of N-{2-(3-)-2-pyridine radicals) ethyl-
-tri-fluoro-O-toluamides }, by hindering the electronics transfer of succinate dehydrogenase in respiratory chain, suppress mitochondrial respiratory.Be mainly used in preventing and treating on broad leaf crop the microbial disease of capsule.To the downy mildew on the vegetables such as cucumber, custard squash, powdery mildew, the downy mildew of fruit tree etc. causes that by germ multiple diseases has favorable effect.
Bupirimate belongs to miazines systemic fungicide, has protection and therapeutic action.Its chemical name is 5-normal-butyl-2-ethyl amido-6-methylpyrimidine-4-base dimethylamino sulphonic acid ester, and bupirimate can be absorbed rapidly by plant roots, stem, leaf, and in plant corpus, runs to each position, therefore resistance of rainwater washing against.Have that consumption is few, efficient, low toxicity, powdery mildew had to the advantages such as special efficacy, be suitable for the various powdery mildews of the ornamental plantss such as fruit tree, vegetables, flowers, field crop.
In the real process of agricultural production, using chemical agent is the most effectively means of control plant pest, but the problem the most easily producing by chemical control disease is the generation of disease drug resistance.In the chemical control of bacteriosis, years of researches have been carried out both at home and abroad, although some antibacterium medicaments have started to enter practical stage, but the medicament of chemosynthesis has long, the shortcoming such as cost is high, toxicity is large, environmental pollution is serious of cycle, can not meet the requirement of agricultural sustainable development far away.And long-term use single pesticidal preparations continuously high dose, easily cause the problems such as residual, the environmental pollution of medicament and resistance to pesticide resistance fungi development.And by contrast, exploitation is efficient with research, low toxicity, low-residual composite be mixed there is small investment, the lead time is short and be subject to domestic and international attention, the numerous and confused dynamics that develops that strengthens.We filter out fluorine pyrrole bacterium acid amides and bupirimate and carry out compositely on the basis of lab screening and field trial, have obvious synergistic effect.And about the composite composition pesticide of fluorine pyrrole bacterium acid amides and bupirimate and application, there is no at present people reported.
Summary of the invention
Based on above situation, the object of the invention is to provide a kind of new and effective composition pesticide, effectively controls the diseases such as powdery mildew on vegetables, field crop, downy mildew.
Technical scheme of the present invention realizes by following measures:
A bactericidal composition that contains fluorine pyrrole bacterium acid amides and bupirimate, active ingredient fluorine pyrrole bacterium acid amides and two yuan of the bupirimates of this composition pesticide are composite, and all the other are auxiliary element.In wherein said composition pesticide, the mass ratio of active ingredient fluorine pyrrole bacterium acid amides and bupirimate is 1～50: 50～1, described composition pesticide of the present invention is through toxicity test experimental verification, the mass ratio of fluorine pyrrole bacterium acid amides and bupirimate is 1～10: 10～1 o'clock, and synergistic effect is optimum.
The formulations of pesticide that described composition pesticide of the present invention can be prepared are missible oil, suspending agent, wetting powder, water dispersible granules, aqueous emulsion, microemulsion, granule, microcapsule formulations, aqua.Wherein active ingredient fluorine pyrrole bacterium acid amides and the gross mass of bupirimate in preparation account for 1%～80% of the whole quality of the pharmaceutical preparations, while wherein accounting for 1%～50%, and toxicity and residually reach good balance, cost is also lower.
The specific embodiments of the formulations of pesticide that composition pesticide of the present invention is mixed with is as follows:
Described bactericidal composition is cream preparation, and the mass fraction of component is: 1～50 part of fluorine pyrrole bacterium acid amides; 1～50 part of bupirimate; 10～30 parts of conventional emulsifiers; 20～50 parts of conventional solvents; 1～5 part of conventional synergist.The concrete production stage of this cream preparation is for first adding active ingredient fluorine pyrrole bacterium acid amides and bupirimate in solvent the oily liquids that becomes transparent and homogeneous after adding again emulsifier, synergist to stir after dissolving completely, filling, can be made into the cream preparation of the present composition.
Described bactericidal composition is suspending agent, and the mass fraction of component is: 1～50 part of fluorine pyrrole bacterium acid amides; 1～50 part of bupirimate; 5～20 parts of dispersants; 1～5 part of antifreezing agent; 0.1～2 part of thickener; 0.1～0.8 part of defoamer; 0～10 part of penetrating agent; 0.1～5 part of pH value conditioning agent; Water, surplus.The concrete production stage of this suspending agent is for first mixing other auxiliary agents, through high speed shear, mix, add active ingredient fluorine pyrrole bacterium acid amides and bupirimate, in ball crusher, abrading-ball is 2～3 hours, make a diameter all below 5mm, can be made into the suspending agent preparation of the present composition.
Described bactericidal composition is wetting powder, and the mass fraction of component is: 1～50 part of fluorine pyrrole bacterium acid amides; 1～50 part of bupirimate; 3～10 parts of dispersants; 1～5 part of wetting agent; Filler, surplus.The concrete production stage of this wetting powder is: by above-mentioned formula, active ingredient fluorine pyrrole bacterium acid amides is mixed with bupirimate and dispersant, wetting agent and filler, uniform stirring in stirred tank, after airslide disintegrating mill, mixing, can be made into the wetting powder of the present composition.
Described bactericidal composition is water dispersible granules, and the mass fraction of component is: 1～50 part of fluorine pyrrole bacterium acid amides; 1～50 part of bupirimate; 3～10 parts of dispersants; 1～10 part of wetting agent; 1～5 part of disintegrant; Filler, surplus.The concrete production stage of this water dispersible granules is: by above-mentioned formula, active ingredient fluorine pyrrole bacterium acid amides is mixed with bupirimate and dispersant, wetting agent, disintegrant and filler, with micro jet, pulverize, through mediating, then add and in fluidized bed prilling dryer, carry out granulation, dry, screening by sample analysis, can be made into the water dispersible granules of the present composition.
Described bactericidal composition is aqueous emulsion, and the mass fraction of component is: 1～50 part of fluorine pyrrole bacterium acid amides; 1～50 part of bupirimate; 3～30 parts of emulsifier; 5～15 parts of solvents; 2～15 parts of stabilizing agents; 1～5 part of antifreezing agent; 0.1～8 part of defoamer; 0.2～2 part of thickener; Water, surplus.The concrete production stage of this aqueous emulsion is: first fluorine pyrrole bacterium acid amides and bupirimate, solvent and emulsifier, cosolvent are added together, make to be dissolved into uniform oil phase; By part water, antifreeze, other the insecticides adjuvant such as antimicrobial mixes into uniform water; When reactor high speed stirs, oil phase is added to water, slowly add water until reach phase inversion point, open clipper and carry out high speed shear, and add remaining water, shear about half an hour, form the aqueous emulsion of oil-in-water type, can be made into the aqueous emulsion of the present composition.
Described bactericidal composition is microemulsion, and the mass fraction of component is: 1～50 part of fluorine pyrrole bacterium acid amides, 1～50 part of bupirimate, 10～30 parts of emulsifier, 1～8 part of antifreezing agent, 0.5～10 part of stabilizing agent, 20～50 parts of conventional solvent cosolvents.Fluorine pyrrole bacterium acid amides and bupirimate are dissolved completely with cosolvent, then add other compositions such as emulsifier, antifreezing agent stabilizing agent, evenly mix, finally add water, after fully stirring, can be made into microemulsion.
Described bactericidal composition is granule, and the mass fraction of component is: 1～50 part of fluorine pyrrole bacterium acid amides, 1～50 part of bupirimate, 1～10 part of wetting dispersing agent; 0.1～5 part of thickener; 0.1～5 part of defoamer; Castor oil, surplus is supplied.Each components such as active ingredient fluorine pyrrole bacterium acid amides and bupirimate, dispersant, stabilizing agent, defoamer and solvent are mixed in the ratio of formula, put into after the grinding of sand milling still, send in mixer for well-distribution and mix and get product.
Described bactericidal composition is microcapsule formulations, and the mass fraction of component is: 1～50 part of fluorine pyrrole bacterium acid amides, 1～50 part of bupirimate, 5～20 parts, urea; 5～20 parts, formaldehyde; 5～20 parts of emulsifying dispersants; 1～5 part of antifreezing agent; 0.1～2 part of thickener; 0.1～0.8 part of defoamer; Water, surplus.In being housed, the there-necked flask of agitating device adds urea and formaldehyde (amount of substance ratio is about l:1.5～2.0), left and right, pH value to 8～9 with sodium hydroxide solution regulator solution, then be warming up to 70～80 ℃, reaction obtains stable urea resin prepolymer.Get a certain amount of fluorine pyrrole bacterium acid amides and bupirimate and be dissolved in cyclohexane, and add emulsifying dispersant in solution, follow vigorous stirring, the O/W type stable emulsion that to be made into the aqueous solution of take containing emulsifying dispersant be water.Above-mentioned urea resin prepolymer is added in emulsion, regulate pH value, polymerization reaction take place under acid catalysis condition, is wrapped oil phase substance, forms microcapsule granule.Slowly heat up, solidify, temperature is controlled at 40～50 ℃, hardening time 1h.Selection adds appropriate auxiliary agent, the microcapsules that gets final product stablely.
Described sterilization worm composition is aqua, and the mass fraction of component is: 1～50 part of fluorine pyrrole bacterium acid amides, 1～50 part of bupirimate, 0.1～30 part of wetting dispersing agent; 2～8 parts of antifreezing agents; 0.1～1 part of defoamer; 0.1～3 part of thickener; 5～15 parts of spreader-stickers; Water, surplus is supplied.By active ingredient fluorine pyrrole bacterium acid amides and bupirimate, dissolve completely with cosolvent, then add other compositions such as dispersant, antifreezing agent, defoamer, evenly mix, finally add water, after fully stirring, get final product to obtain finished product.
Wherein above-described emulsifier is selected from calcium dodecyl benzene sulfonate and aliphatic acid polyethenoxy ether, alkylphenol polyoxyethylene sulfosuccinate, styrylphenol polyoxyethylene ether, polyoxyethylene nonylphenol ether, castor oil polyoxyethylene ether, aliphatic acid polyethenoxy base ester, any or more than one any mixtures than forming in polyoxyethylene aliphatic alcohol ether.
Described solvent is dimethylbenzene or biodiesel, toluene, diesel oil, methyl alcohol, ethanol, n-butanol, isopropyl alcohol, turpentine-based vegetable oil code name is ND-45, solvent naphtha, dimethyl formamide, dimethyl sulfoxide (DMSO), one or more in water equal solvent are arbitrarily than the mixture forming.
It is LG-3, GY-D1252, GY-D1256, SNWGF-01 that described dispersant is selected from polycarboxylate code name, lignosulfonates code name is 201107,201108, alkylphenol polyoxyethylene methyl ether condensate sulfate, alkylsulfonate calcium salt, naphthalene sulfonic acid-formaldehyde condensation product sodium salt, alkylphenol polyoxyethylene, polyoxyethylene carboxylate, aliphatic amine polyoxyethylene ether, one or more in fatty acid glyceride APEO.
Described wetting agent is selected from lauryl sodium sulfate, calcium dodecyl benzene sulfonate, and Nekal BX, moistening bleeding agent F, alkylbenzenesulfonate polyoxyethylene triphen is phosphenylic acid salt dimly, spaonin powder, silkworm excrement, one or more in soapberry powder.
Described disintegrant is selected from bentonite, urea, ammonium sulfate, aluminium chloride, citric acid, succinic acid, one or more in sodium bicarbonate.
Described thickener is selected from xanthans, carboxymethyl cellulose, carboxyethyl cellulose, methylcellulose, Magnesiumaluminumsilicate, in polyvinyl alcohol one or more.
Described stabilizing agent is selected from sodium citrate, a kind of in resorcinol.
Described antifreezing agent is selected from ethylene glycol, propane diols, one or more in glycerine.
Described defoamer is selected from silicone oil, silicone compound, C
10-20saturated fat acid compounds, C
8-10one or more of fatty alcohol.
Described filler is selected from kaolin, diatomite, bentonite, attapulgite, white carbon, starch, one or more in precipitated calcium carbonate.
The present invention be take the composite bactericide that fluorine pyrrole bacterium acid amides and bupirimate be active ingredient and is had obvious synergistic effect, delay the drug-fast generation in key, and reduced and become to have produced cost and use cost, effectively control the diseases such as powdery mildew on vegetables, field crop, downy mildew.
Embodiment
For making technical scheme of the present invention, object and advantage are clearer, and the present invention describes with following specific embodiment, but the present invention is not limited to these examples.The mode that effect experiment of the present invention adopts indoor biometrics and field trial to combine, if no special instructions, the ratio of below mentioning is all ratio of quality and the number of copies.
Embodiment: fluorine pyrrole bacterium acid amides proportioning co-toxicity experiments different from bupirimate.
1.1 reagent agent
The former medicine of 95% fluorine pyrrole bacterium acid amides, the former medicine of 95% bupirimate, above-mentioned former medicine provides by research and development department of extra large rel medicine company limited company.
1.2 test targets
From Shouguang, Shandong, never executed fluorine pyrrole bacterium acid amides and bupirimate and cucumber of the same type gather potted plantly separated, for examination cucumber variety: Chang Chun Mi Ci.
1.3 test method
1.3.1 medicament preparation
First use the former medicine of acetone solution, according to the result of preliminary experiment, two appropriate former medicines are made into several different proportionings, then it is stand-by with acetone, each processing to be diluted to respectively to several concentration gradients.
Susceptible cucumber variety Chang Chun Mi Ci cultivation, in pot for growing seedlings, is placed in to greenhouse and cultivates, and plant grows to three to four leaf after dates, gathers the blade of identical leaf age, for cultivation and the mensuration of cucumber downy mildew germ.
1.3.2 the cultivation of cucumber downy mildew germ and the preparation of spore suspension
Cucumber downy mildew germ adopts plants method to cultivate under 20 ℃, the condition of 12h alternation of light and darkness, and every 30 d turn culture 1 time.During inoculation, with the conidium on sterile water wash-out incidence of leaf, being mixed with spore concentration is l * 10
6the suspension of individual/mL.
1.3.3 strains tested sensitivity testing
Adopt leaf dish moisturizing method to carry out toxicity test.First the blade of collection is prepared into the leaf dish that diameter is 1.5cm, mix at random, be placed in respectively the series concentration liquid configuring and soak lh, 50 leaf dishes of each concentration, test is with the blank that is treated to of adding medicine not, after immersion finishes, leaf faces up and puts on the wetting blotting paper of identical liquor strength, liquid on leaf dish is blotted, the spore suspension l0L preparing is inoculated in to leaf dish central authorities, and room temperature is placed after 5 min, is placed under 20 ℃, the condition of 1 2h alternation of light and darkness and cultivates, after 10d, measure the onset area on leaf dish, calculate EC
50.
The percentage that accounts for leaf disc area according to lesion area is divided sick level
0 grade: anosis;
1 grade: sorus area accounts for below 5% of whole leaf area;
3 grades: sorus area accounts for below the 6%-10% of whole leaf area;
5 grades: sorus area accounts for below the 11%-20% of whole leaf area;
7 grades: sorus area accounts for below the 21%-50% of whole leaf area;
9 grades: sorus area accounts for the more than 50% of whole leaf area;
1.3.4 mixture toxicity test and interpretation of result
By single dose toxicity test method, according to mixed ratio, carry out the toxicity test of mixture.
If contrast lethality <5%, does not proofread and correct, contrast lethality, between 5%-20%, is proofreaied and correct by formula 2, contrast lethality >20%, and test need be reformed.
The logarithm value of drug concentration (mg/L) of take is independent variable x, and the probability value of corrected mortality of take is dependent variable y, sets up respectively virulence regression equation formula, adopts DPS software to calculate the EC of single dose and each proportioning mixture
50according to the abundant method of Sun Yun, calculate co-toxicity coefficient (CTC).Co-toxicity coefficient CTC, computing formula is as follows: (the fluorine pyrrole bacterium acid amides of take is standard medicament, and its toxicity index is 100):
The EC of the toxicity index of bupirimate (TI)=fluorine pyrrole bacterium acid amides
50the EC of/bupirimate
50* 100
The EC of true toxicity index (ATI)=fluorine pyrrole bacterium acid amides of M
50the EC of/M
50* 100
TI * P bupirimate of TI * P fluorine pyrrole bacterium acid amides+bupirimate of theoretical toxicity index (TTI)=fluorine pyrrole bacterium acid amides of M
TTI * 100 of the ATI/M of the co-toxicity coefficient of M (CTC)=M
In formula:
M is fluorine pyrrole bacterium acid amides and the mixture of the different proportionings of bupirimate
P fluorine pyrrole bacterium acid amides is fluorine pyrrole bacterium acid amides shared ratio in mixture
P bupirimate is bupirimate shared ratio in mixture.
2.1 toxicity test results
Table 1 fluorine pyrrole bacterium acid amides and the toxicity test of bupirimate to cucumber downy mildew
As can be seen from the table, the result of the test of different proportion proportioning shows, in active ingredient ratio, dilute respectively and all show stronger synergistic effect, wherein take fluorine pyrrole bacterium acid amides: bupirimate as 1:10～10:1 time synergistic effect best, suggestion is carried out further field control effectiveness test to suitable proportion 1:10～10:1 left and right mixture preparation, to evaluate its field practical application effect.
3, the experimental result of field trial control wheat powdery mildew, cucumber downy mildew
3.1 field trial control wheat powdery mildews
3.1.1 test method
Test site, in great Tong Qiao village, capital town, Fengyang County, is wheat for studying thing, and kind is short morning 781, broadcasts sowing, and growing way is better, and test is established every mu and established contrast totally 10 processing.Every processing repeats 4 times, and random district group is arranged, 30 square metres of community areas.
3.1.2 control time and number of times
Before dispenser, after the 1st medicine after 7 days and the 2nd dispenser 7 days, 14 days, every community adopted 5 samplings of diagonal, every some investigation 20 strains, before blooming, 2 leaves are got in every strain from upper end, after blooming, sword-like leave 2 leaves are got in every strain, by leaf classification investigation occurring degree, calculate disease and refer to and control efficiency.
Grade scale is as follows:
0 grade: anosis;
1 grade: lesion area accounts for below 5% of one-piece blade area;
3 grades: lesion area accounts for the 6%-15% of one-piece blade area;
5 grades: lesion area accounts for the 16%-25% of one-piece blade area;
7 grades: lesion area accounts for the 26%-50% of one-piece blade area;
9 grades: lesion area accounts for the more than 50% of one-piece blade area.
3.1.3 drug effect computational methods
The total number of sheets * 100 of sick leaf rate (%)=sick number of sheets/investigate
Disease index=∑ (the sick number of sheets * relative level numerical value at different levels)/(investigating the total number of sheets * 9) * 100
Control efficiency (%)=(disease index after the front disease index * treatment region medicine of 1-(blank district medicine)/(the front disease index of disease index * treatment region medicine after blank district medicine)) * 100.
3.1.4 poisoning investigation method
After dispenser, whether 14d range estimation medicament has poisoning to crop continuously.
3.1.5 result of the test and analysis
Each processes the effect of control wheat powdery mildew.
As shown in Table 2 fluorine pyrrole bacterium acid amides and bupirimate composite bactericide for wheat powdery mildew control successful higher than fluorine pyrrole bacterium acid amides and bupirimate single dose, bactericidal effect increases progressively with the increase of dosage.According to field range estimation, within the scope of test dose, plant growth is normal, and the poisoning phenomenon to wheat does not all appear in each treatment agent, illustrates that it is safe to wheat.Advise that the bactericide different from the mechanism of action mixes use to delay the drug-fast generation of germ.
3.2 field trial control cucumber downy mildews
3.2.1 test method
Test is on Shandong Pingdu City cucumber ground, and test kind is middle peasant No. 8, and every processing repeats for 4 times, 5 points of every community double diagonal line investigation, and every some investigation 3 strain cucumber, record occurring degree by staging, and grade scale is as follows:
0 grade: anosis;
1 grade: scab heap area accounts for below 5% of whole leaf area;
3 grades: scab heap area accounts for below the 6%-10% of whole leaf area;
5 grades: scab heap area accounts for below the 11%-20% of whole leaf area;
7 grades: scab heap area accounts for below the 21%-50% of whole leaf area;
9 grades: scab heap area accounts for the more than 50% of whole leaf area.
3.2.2 control time and number of times
Test is investigated 4 times altogether, and radix investigation before medicine is investigated after 7 days, 7 days for the second time and medicine after medicine for the first time for 15 days.
3.2.3 drug effect computational methods
The total number of sheets * 100 of sick leaf rate (%)=sick number of sheets/investigate
Disease index=∑ (the sick number of sheets * relative level numerical value at different levels)/(investigating the total number of sheets * 9) * 100
Control efficiency (%)=(disease index after the front disease index * treatment region medicine of 1-(blank district medicine)/(the front disease index of disease index * treatment region medicine after blank district medicine)) * 100.
3.2.4 poisoning investigation method
After dispenser, whether 15d range estimation medicament has poisoning to crop continuously.
3.2.5 result of the test and analysis
Table 3 different disposal is prevented and treated measurement result to cucumber downy mildew
By above field experiment, show, fluorine pyrrole bacterium acid amides and bupirimate complex preparation are obviously better than single dose for the preventive effect of cucumber downy mildew, and bactericidal effect increases progressively with the increase of dosage.According to field range estimation, within the scope of test dose, plant growth is normal, without poisoning situation, occurs, significant for agricultural produce, is worthy to be popularized.
In sum, the bactericidal composition that the present invention contains fluorine pyrrole bacterium acid amides and bupirimate, has good control efficiency to wheat powdery mildew, cucumber downy mildew, and it is to target crop safety.Complex preparation has not only improved preventive effect, and has expanded the control to bacterium, so this compounded combination tool in production practices is of great significance.
Claims (4)
1. a bactericidal composition that contains fluorine pyrrole bacterium acid amides and bupirimate, it is characterized in that: the active ingredient of this composition pesticide is fluorine pyrrole bacterium acid amides and bupirimate binary built, all the other are auxiliary element, and wherein the mass ratio of active ingredient fluorine pyrrole bacterium acid amides and bupirimate is 1～50: 50～1.
2. composition pesticide according to claim 1, is characterized in that: fluorine pyrrole bacterium acid amides and the gross weight of bupirimate in preparation account for 1%～80% of the whole quality of the pharmaceutical preparations.
3. composition pesticide according to claim 2, is characterized in that: fluorine pyrrole bacterium acid amides and the gross weight of bupirimate in preparation account for 1%～50% of the whole quality of the pharmaceutical preparations.
4. according to the composition pesticide described in claim 1 or 2 or 3, it is characterized in that: the formulation of this composition pesticide is missible oil, suspending agent, wetting powder, water dispersible granules, aqueous emulsion, microemulsion, microcapsule formulations, granule, aqua
.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310685651.4A CN103688938A (en) | 2013-12-16 | 2013-12-16 | Bactericidal composition containing fluopyram and bupirimate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310685651.4A CN103688938A (en) | 2013-12-16 | 2013-12-16 | Bactericidal composition containing fluopyram and bupirimate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN103688938A true CN103688938A (en) | 2014-04-02 |
Family
ID=50350731
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201310685651.4A Pending CN103688938A (en) | 2013-12-16 | 2013-12-16 | Bactericidal composition containing fluopyram and bupirimate |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN103688938A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105994281A (en) * | 2016-05-26 | 2016-10-12 | 南京华洲药业有限公司 | Antibacterial composition containing C15H8ClF7N2O2 and bupirimate as well as application of antibacterial composition |
| CN108684679A (en) * | 2018-07-07 | 2018-10-23 | 安徽省农业科学院植物保护与农产品质量安全研究所 | A kind of microbicide compositions of containing fluopyram |
-
2013
- 2013-12-16 CN CN201310685651.4A patent/CN103688938A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105994281A (en) * | 2016-05-26 | 2016-10-12 | 南京华洲药业有限公司 | Antibacterial composition containing C15H8ClF7N2O2 and bupirimate as well as application of antibacterial composition |
| CN108684679A (en) * | 2018-07-07 | 2018-10-23 | 安徽省农业科学院植物保护与农产品质量安全研究所 | A kind of microbicide compositions of containing fluopyram |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN103271031A (en) | Sterilization composition containing cyanoacrylate bactericide and metalaxyl-M | |
| CN103355333A (en) | Sterilization composition containing pyraclostrobin and boscalid | |
| CN105409963A (en) | Sterilization composition containing efficient metalaxyl-M and azoxystrobin | |
| CN103719102A (en) | Sterilization composite containing fluopyram and prothioconazole | |
| CN103918653A (en) | Bactericidal composition containing picoxystrobin and procymidone | |
| CN103918694A (en) | Bactericidal composition containing iprodione and metalaxyl-M | |
| CN103229767A (en) | Trifloxystrobin and bupirimate-containing sterilization composition | |
| CN103141493A (en) | Bactericidal composition containing difenoconazole and benthiavalicarb-isopropyl | |
| CN103688938A (en) | Bactericidal composition containing fluopyram and bupirimate | |
| CN103688951A (en) | Bactericidal composition containing fluopyram and pyrisoxazole | |
| CN103688965A (en) | Bactericidal composition containing fluopyram and pyraclostrobin | |
| CN103783046A (en) | Fungicidal composition containing prothioconazole and pyrimethanil | |
| CN103931640A (en) | Bactericidal composition containing meptyldinocap and pyraclostrobin | |
| CN103503879A (en) | Sterilization composition containing prothioconazole and bupirimate | |
| CN104054708A (en) | Bactericidal composition containing meptyldinocap and spiroxamine | |
| CN103975928A (en) | Bactericidal composition containing meptyldinocap and penconazole | |
| CN103355316A (en) | Bactericide composition containing N-methyl-3-(4-chloro)phenyl-5-methyl-5-pyridyl-3-methyl-oxazoline and methyl (E)-2-(2-((3-(4-chlorphenyl)-1-methyl-1H-pyrazolyl-5-oxy)methyl)phenyl-3-methoxyacrylate | |
| CN103688939A (en) | Bactericidal composition containing fluopyram and ethirimol | |
| CN103688937A (en) | Bactericidal composition containing fluopyram and triflumizole | |
| CN103798244A (en) | Bactericidal composition containing cyflufenamid and flutriafol | |
| CN103798256A (en) | Bactericidal composition containing cyflufenamid and thifluzamide | |
| CN104126593A (en) | Sterilization composition containing ametoctradin and fluopyram | |
| CN103918679A (en) | Bactericidal composition containing thifluzamide and procymidone | |
| CN103734160A (en) | Sterilization composition containing benthiavalicarb isopropyl and zineb | |
| CN104041494A (en) | Bactericidal composition containing meptyldinocap and bupirimate |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| WD01 | Invention patent application deemed withdrawn after publication | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20140402 |