CN102379290A - Ultralow volume liquid containing chlorantraniliprole - Google Patents

Ultralow volume liquid containing chlorantraniliprole Download PDF

Info

Publication number
CN102379290A
CN102379290A CN2011102699801A CN201110269980A CN102379290A CN 102379290 A CN102379290 A CN 102379290A CN 2011102699801 A CN2011102699801 A CN 2011102699801A CN 201110269980 A CN201110269980 A CN 201110269980A CN 102379290 A CN102379290 A CN 102379290A
Authority
CN
China
Prior art keywords
low volume
ultra low
rynaxypyr
volume liquids
diazinon
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.)
Granted
Application number
CN2011102699801A
Other languages
Chinese (zh)
Other versions
CN102379290B (en
Inventor
黄华
卢镇
朱华龙
王群利
唐卫
李现玲
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.)
Guangxi Tianyuan Biochemical Co Ltd
Original Assignee
Guangxi Tianyuan Biochemical 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 Guangxi Tianyuan Biochemical Co Ltd filed Critical Guangxi Tianyuan Biochemical Co Ltd
Priority to CN 201110269980 priority Critical patent/CN102379290B/en
Publication of CN102379290A publication Critical patent/CN102379290A/en
Application granted granted Critical
Publication of CN102379290B publication Critical patent/CN102379290B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The invention discloses ultralow volume liquid containing chlorantraniliprole, which is prepared by using chlorantraniliprole or synergistic compound of the chlorantraniliprole and diazinon as an activated ingredient and adding solvent, solubilizer, pesticide damage reducer, easer and penetrant. In the compound, weight ratio of the chlorantraniliprole to the diazinon of the activated ingredient is 1:4 to 1:50. The ultralow volume liquid containing chlorantraniliprole has the advantages of simplicity in processing, long-term effect, high efficiency, enabling a target being not easy to resist the pesticide, low environmental pollution, synergetic interaction and the like. Application of ultralow volume spray, low volume spray or ultralow volume static spray can control various pests such as chilo suppressalis, tryporyza incertulas, cnaphalocrocis medinalis, ostrinia furnacalis, ostrinia nubilalis, macrosiphum avenae, rhopalosiphum padi and the like.

Description

A kind of chloride worm benzamide ultra low volume liquids
Technical field
The invention belongs to technical field of pesticide, specifically relate to the ultra low volume liquids of chloride worm benzamide.
Background technology
Rynaxypyr is the O-formammidotiazol-benzamide broad spectrum pesticide, and the target of effect is the ryania acceptor, and Rynaxypyr makes insect ryania receptor channel be in lasting open state; Cause calcium ion and in the sarcoplasmic reticulum chamber, discharge in a large number, destroyed the stable of the interior environment of cytoplasm calcium ion, thereby make the imbalance of insect contraction of muscle; Insect stops to get food rapidly in the effect back; Muscular paralysis occurs, be slow in action, paralysis is until last death.Learn in the characteristic at the different pharmaceutical that Rynaxypyr produces, these change all is to be different from the binding site mediation of ryania on the ryania acceptor by one, and the effect of this insecticide is highly single-minded to insect ryania acceptor, produces to select toxicity.The Rynaxypyr structure is unique, and the mode of action is novel, and insecticidal spectrum is wide, and is effective to lepidoptera pest, and selectivity is good, to various beneficial insects and natural enemies security, and does not have cross resistance with used insecticide, is suitable for the resistance management and the insect comprehensive regulation.But Costco Wholesale is difficult to be widely used on the crop pest control than higher at present.
Diazinon has another name called diazinon; Be broad-spectrum organic insecticide, have tag, stomach toxicity, stifling and certain systemic function, according to its characteristic; On agricultural, be used to prevent and treat sucking pest, defoliator and soil insect; Can prevent and treat cotton cotten aphid, two spotted spider mite, water rice hopper, rice-leaf hopper, rice-stem borer, and corn, wheat, peanut soil pest, use is also being arranged aspect gardens and the herding.But how to use with the missible oil formulation at present, missible oil uses a large amount of aromatic hydrocarbon, promotes the use of environment is caused very big pressure.
The insecticide of Rynaxypyr and diazinon synergistic complex is not arranged at present as yet, and more not seeing has the report that it is prepared into ultra low volume liquids.Synergistic complex is that insecticide enlarges insecticidal spectrum, improves insecticidal effect, administers pest resistance, reduces a kind of effective way of use cost.Ultra low volume liquids (Ultra low volume Concentrate; Hereinafter to be referred as ULV), be a kind of special finish, be with the effective dispersion medium of high boiling oily solvent as agricultural chemicals; Add auxiliary agent and process, generally contain higher pesticide activity component content.On ground or with aircraft through ultra low volume liquid sprayer with the fine mist that ULV sprays into 70~120 μ m, be evenly distributed on the surface of plant stem-leaf, thereby performance anti-is cured the disease effectively, the effect of insect pest.The use work efficiency of ultra low volume liquids is high, and expenses for prevention and control is low, and dispenser does not need water, energy-saving and environmental protecting, and cost is low.
But present domestic cultural control damage by disease and insect is general is the regular dosage form time conventional spray-on process of employing, and it is that pesticidal preparations is carried out the extermination of disease and insect pest afterwards with big water gaging dilution, and there is many-sided defective in this method of preventing and treating:
1, conventional spray-on process work efficiency is low, and work efficiency is merely 2~5 mu/day per capita usually, is difficult to satisfy the needs of large-scale planting.
2, conventional spray-on process prevention and elimination of disease and pests needs big water gaging, and water consumption reaches 450~900L/hm usually 2, and regional away from water source and drought and water shortage a lot, conventional spray-on process is difficult to carry out or can not reaches desirable control efficiency.
3, conventional spray-on process makes the with medicament lasting period short, because conventional spray-on process makes the formulation of with medicament be generally missible oil, aqua, wetting powder, suspending agent, aqueous emulsion etc., has certain defective in the use:
(1) owing to add big water gaging dilution, the concentration of soup is very low, and surface tension is often bigger, and is relatively poor in the crop that wax coat is arranged or the lip-deep adhesiveness of target, wetability, permeability, is difficult to effectively get in crop and the target body, causes preventive effect relatively poor;
(2) in the natural environment of illumination, high temperature, drying, the water in the soup is easy to evaporation, causes medicament only to remain in crop surface, comes off and loses efficacy from crop easily after photodissociation and the drying easily;
(3) mist droplet particle size of conventional spraying is bigger, reaches 200~600 μ m, causes being sprayed onto the lip-deep soup of crop or target and runs off easily.
(4) for a long time, the single and frequent use of pesticide species makes biological target grow with each passing day to the resistance of medicament itself, is unfavorable for the prevention and control to pest.
Summary of the invention
The objective of the invention is that the work efficiency that the conventional pesticide preparation adopts conventional spray-on process prevention and elimination of disease and pests to exist is low, labour intensity big in order to overcome, need water many, prevent that defectives such as heterodynes, lasting period weak point, resistance provide a kind of chloride worm benzamide ultra low volume liquids; Its water consumption is few; Droplet is little; Control efficiency is good, and control efficiency is good, uses the Synergistic insecticidal with clear superiority in large tracts of land use or water-deficient area.
A kind of chloride worm benzamide ultra low volume liquids of the present invention is with Rynaxypyr; Or Rynaxypyr and diazinon synergistic complex are active component; The ultra low volume liquids that adding solvent, solubilizer, reduction poisoning agent, viscosity reductant, bleeding agent are prepared into, the percentage by weight of each component is:
Rynaxypyr 0.1%-8% solvent 40%-80%
Solubilizer 1%-15% reduces poisoning agent 1%-15%
Viscosity reductant 1%-5% bleeding agent 1%-5%;
Or:
The weight ratio of described Rynaxypyr and diazinon is 1: 4-1: 50, and optimum ratio is 1: 15-1: 28.
The proportioning that preferred Rynaxypyr accounts for gross weight is that the proportioning that 0.5%-3%, diazinon account for gross weight is 10%-20%.
Said solvent is diethyl succinate and terebinthine combination, and its weight proportion is 1-3: 3-1.
Said solubilizer is N-Methyl pyrrolidone, N, one or more combinations in dinethylformamide, the DMAC N,N; Said reduction poisoning agent is vegetable oil such as Jatropha curcas oil, soybean oil, cottonseed oil, rapeseed oil, castor-oil plant wet goods; Said viscosity reductant is n-butanol or other alcohols such as n-octyl alcohol, ketone such as cyclohexanone, ethers such as butyl glycol ether; Said bleeding agent is an AEO.
Preparation method of the present invention is under the normal temperature and pressure; In reaction vessel, add solvent, active component sequentially with electronic stirring; Be sequentially added into solubilizer, bleeding agent, viscosity reductant, reduction poisoning agent under stirring; Wait to dissolve continued and stirred 15-30 minute, the liquid that obtains the stable transparent shape at last is the ultra low volume liquids of chloride worm benzamide; The speed of agitator that adopts among the preparation method is 100-120r/min.
The present invention is adapted at preventing and treating in rice-stem borer, paddy stem borer, leaf roll snout moth's larva, Asiatic corn borer, European corn borer, little English grain aphid, standing grain Rhopalosiphum spp, Sugarcane Yellow snout moth's larva, pink rice borer, bar snout moth's larva, white snout moth's larva, the chilo infuscatellus and uses.
Application process of the present invention is ultra low volume spraying, low-gallonage spraying or ultra low volume electrostatic spray.
The invention has the beneficial effects as follows:
1, water is few, and the present invention blends with adding water in the process of spraying hardly, but directly medicament is sprayed onto on the blade and stem stalk of crop, and through damage by disease and insect target is convenient away from water source and drought and water shortage area dispenser.
2, work efficiency is high, through using the ultra low volume sprayer dispenser, can increase substantially efficient, improve work efficiency several times to tens times, reduce cost of labor, effectively lower labour intensity.
3, drug concentration is high, and the lasting period is long.The content of conventional dose own is high; It is low to blend the soup units activity component content that sprays after the water, and ultra low volume is directly with reagent spray, and the active component content of medicament own is low; But the units activity constituent concentration content of spraying liquor is high, helps improving drug effect; Secondly, ultra low volume adopts low-volatile oil to make solvent, and active component is penetrated into the blade deep layer, and resistance of rainwater washing against prolongs the lasting period, thereby reduces the medication number of times, reduces agricultural cost.
4, Synergistic: Rynaxypyr and diazinon belong to the insecticide of different effects mechanism, and their composite synergistic functions that plays improve quick-acting, and the expanding prevention target is composed, and delays the pesticide resistance of insect, reduces the pollution of environment.
5, droplet is little, and ultra low volume electrostatic spray fogdrop diameter is that 30~60 μ m, ultra low volume ground spraying droplet diameter are 30~80 μ m, aerial ultra low volume spraying fogdrop diameter 30~60 μ m, and conventional spraying droplet diameter is many more than 200~600 μ m.
6, to crop safety.Ultra low volume spraying be difficult for to produce poisoning to crop safety, does not have obviously residually, can improve crop quality.
Embodiment
The present invention describes with the following example, but does not limit the scope of the invention.
Embodiment 1:
0.1% Rynaxypyr ultra low volume liquids
Figure BDA0000090846810000031
Preparation method: under the normal temperature and pressure; In reaction vessel, add solvent, Rynaxypyr sequentially with electronic stirring; Be sequentially added into solubilizer, bleeding agent, viscosity reductant, reduction poisoning agent under stirring; Wait to dissolve continued and stirred 15 minutes, the liquid that obtains the stable transparent shape at last is for containing 0.1% Rynaxypyr ultra low volume liquids; The speed of agitator that adopts among the preparation method is 120r/min.
Embodiment 2:
2% Rynaxypyr ultra low volume liquids
Figure BDA0000090846810000042
Preparation method: under the normal temperature and pressure; In reaction vessel, add solvent, Rynaxypyr sequentially with electronic stirring; Be sequentially added into solubilizer, bleeding agent, viscosity reductant, reduction poisoning agent under stirring; Wait to dissolve continued and stirred 20 minutes, the liquid that obtains the stable transparent shape at last is for containing 2% Rynaxypyr ultra low volume liquids; The speed of agitator that adopts among the preparation method is 110r/min.
Embodiment 3:
5% Rynaxypyr ultra low volume liquids
Figure BDA0000090846810000043
Preparation method: under the normal temperature and pressure; In reaction vessel, add solvent, Rynaxypyr sequentially with electronic stirring; Be sequentially added into solubilizer, bleeding agent, viscosity reductant, reduction poisoning agent under stirring; Wait to dissolve continued and stirred 30 minutes, the liquid that obtains the stable transparent shape at last is for containing 5% Rynaxypyr liquor; The speed of agitator that adopts among the preparation method is 100r/min.
Embodiment 4:
8% Rynaxypyr ultra low volume liquids
Figure BDA0000090846810000052
Preparation method: under the normal temperature and pressure; In reaction vessel, add solvent, Rynaxypyr sequentially with electronic stirring; Be sequentially added into solubilizer, bleeding agent, viscosity reductant, reduction poisoning agent under stirring; Wait to dissolve continued and stirred 45 minutes, the liquid that obtains the stable transparent shape at last is for containing 8% Rynaxypyr liquor; The speed of agitator that adopts among the preparation method is 100r/min.
Embodiment 5:
40% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000053
Figure BDA0000090846810000061
Preparation method: under the normal temperature and pressure; In reaction vessel, add solvent, Rynaxypyr and diazinon sequentially with electronic stirring; Be sequentially added into solubilizer, bleeding agent, viscosity reductant, reduction poisoning agent under stirring; Wait to dissolve continued and stirred 15 minutes, the liquid that obtains the stable transparent shape at last is for containing 40% Rynaxypyr diazinon ultra low volume liquids; The speed of agitator that adopts among the preparation method is 120r/min.
Embodiment 6:
30.6% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000062
Preparation method: under the normal temperature and pressure; In reaction vessel, add solvent, Rynaxypyr and diazinon sequentially with electronic stirring; Be sequentially added into solubilizer, bleeding agent, viscosity reductant, reduction poisoning agent under stirring; Wait to dissolve continued and stirred 20 minutes, the liquid that obtains the stable transparent shape at last is for containing 30.6% Rynaxypyr diazinon ultra low volume liquids; The speed of agitator that adopts among the preparation method is 110r/min.
Embodiment 7:
5.1% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000063
Preparation method: under the normal temperature and pressure; In reaction vessel, add solvent, Rynaxypyr and diazinon sequentially with electronic stirring; Be sequentially added into solubilizer, bleeding agent, viscosity reductant, reduction poisoning agent under stirring; Wait to dissolve continued and stirred 30 minutes, the liquid that obtains the stable transparent shape at last is for containing 5.1% Rynaxypyr diazinon ultra low volume liquids; The speed of agitator that adopts among the preparation method is 100r/min.
Embodiment 8:
16% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000072
Preparation method: under the normal temperature and pressure; In reaction vessel, add solvent, Rynaxypyr and diazinon sequentially with electronic stirring; Be sequentially added into solubilizer, bleeding agent, viscosity reductant, reduction poisoning agent under stirring; Wait to dissolve continued and stirred 25 minutes, the liquid that obtains the stable transparent shape at last is for containing 16% Rynaxypyr diazinon ultra low volume liquids; The speed of agitator that adopts among the preparation method is 105r/min.
Embodiment 9:
17% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000073
Figure BDA0000090846810000081
The preparation method is with embodiment 1
Embodiment 10:
18% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000082
The preparation method is with embodiment 1
Embodiment 11:
19% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000091
The preparation method is with embodiment 2
Embodiment 12:
20% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000092
The preparation method is with embodiment 2
Embodiment 13:
21% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000093
The preparation method is with embodiment 3
Embodiment 14:
22% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000101
The preparation method is with embodiment 3
Embodiment 15:
23% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000102
The preparation method is with embodiment 4
Embodiment 16:
24% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000103
The preparation method is with embodiment 4
Embodiment 17:
25% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000112
The preparation method is with embodiment 1
Embodiment 18:
26% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000113
The preparation method is with embodiment 1
Embodiment 19:
27% Rynaxypyr diazinon ultra low volume liquids
The preparation method is with embodiment 2
Embodiment 20:
28% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000123
The preparation method is with embodiment 2
Embodiment 21:
29% Rynaxypyr diazinon ultra low volume liquids
The preparation method is with embodiment 3
Embodiment 22:
30% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000132
The preparation method is with embodiment 4
Embodiment 23:
10% Rynaxypyr diazinon ultra low volume liquids
Figure BDA0000090846810000133
Figure BDA0000090846810000141
The preparation method is with embodiment 4
Embodiment 24:
0.1% Rynaxypyr ultra low volume liquids
Figure BDA0000090846810000142
The preparation method is with embodiment 2
Embodiment 25:
5% Rynaxypyr ultra low volume liquids
Figure BDA0000090846810000143
The preparation method is with embodiment 3
Embodiment 26:
8% Rynaxypyr ultra low volume liquids
Figure BDA0000090846810000151
The preparation method is with embodiment 4
Prepared ultra low volume liquids outward appearance is the homogeneous oily liquids of transparence; Low temperature compatibility is good, and under-5 ℃, refrigeration 7d does not separate out crystallization or suspension; Volatility is low, and the filter paper suspension method is measured the result, and volatility is lower than 30%; To plant safety, no poisoning; Viscosity is below 30mPas.
The biologicall test instance
Instance 1: Rynaxypyr and diazinon are measured the co-toxicity coefficient of article sugarcane borer, and experimental result is seen table 1.
The virulence regression equation and the assay thereof of table 1, confession reagent agent
Figure BDA0000090846810000152
Figure BDA0000090846810000161
Conclusion: Rynaxypyr and diazinon are as the SA composition of a kind of ultra low volume liquids among the present invention; By the quality Rynaxypyr: diazinon=1: 31 is a summation action, 1: 15, and 1: 19; 1: 23; 1: 27 for synergistic effect, thereby synergy, particularly Rynaxypyr in it is considered herein that ultra low volume liquids 1: 15~1: 28 scope: diazinon=co-toxicity coefficient reached 502 in 1: 19.

Claims (9)

1. chloride worm benzamide ultra low volume liquids; It is characterized in that: it is with Rynaxypyr; Or Rynaxypyr and diazinon synergistic complex are active component; The ultra low volume liquids that adding solvent, solubilizer, reduction poisoning agent, viscosity reductant, bleeding agent are prepared into, the percentage by weight of each component is:
Rynaxypyr 0.1%-8% solvent 40%-80%
Solubilizer 1%-15% reduces poisoning agent 1%-15%
Viscosity reductant 1%-5% bleeding agent 1%-5%;
Or:
Rynaxypyr 0.1%-8% diazinon 5%-32%
Solvent 40%-80% solubilizer 1%-15%
Reduce poisoning agent 1%-15% viscosity reductant 1%-5%
Bleeding agent 1%-5%.
2. chloride worm benzamide ultra low volume liquids according to claim 1, it is characterized in that: the weight ratio of described Rynaxypyr and diazinon is 1:4-1:50.
3. chloride worm benzamide ultra low volume liquids according to claim 1, it is characterized in that: the weight ratio of said Rynaxypyr and diazinon is 1:15-1:28.
4. chloride worm benzamide ultra low volume liquids according to claim 1 is characterized in that: the proportioning that said Rynaxypyr accounts for gross weight is 0.5%-3%, and the proportioning that diazinon accounts for gross weight is 10%-20%.
5. chloride worm benzamide ultra low volume liquids according to claim 1 is characterized in that: said solvent is that diethyl succinate mixes with terebinthine, and its weight proportion is 1-3: 3-1.
6. chloride worm benzamide ultra low volume liquids according to claim 1, it is characterized in that: said solubilizer is N-Methyl pyrrolidone, N, one or more combinations in dinethylformamide, the DMAC N,N; Said reduction poisoning agent is a vegetable oil, and vegetable oil comprises one or more combinations in Jatropha curcas oil, soybean oil, cottonseed oil, rapeseed oil, the castor oil; Said viscosity reductant is one or more combinations in n-butanol, n-octyl alcohol, cyclohexanone, the butyl glycol ether; Said bleeding agent is an AEO.
7. chloride worm benzamide ultra low volume liquids according to claim 1; It is characterized in that: the preparation method of described ultra low volume liquids does; Under the normal temperature and pressure, in the reaction vessel of band stirring, add solvent, active component sequentially, be sequentially added into solubilizer, bleeding agent, viscosity reductant, reduction poisoning agent under stirring; Wait to dissolve continued and stirred 15-30 minute, the liquid that obtains the stable transparent shape at last is the ultra low volume liquids of chloride worm benzamide; The speed of agitator that adopts among the preparation method is 100-120 r/min.
8. chloride worm benzamide ultra low volume liquids according to claim 1 is characterized in that: its application in control rice-stem borer, paddy stem borer, leaf roll snout moth's larva, Asiatic corn borer, European corn borer, little English grain aphid, standing grain Rhopalosiphum spp, Sugarcane Yellow snout moth's larva, pink rice borer, bar snout moth's larva, white snout moth's larva, chilo infuscatellus.
9. chloride worm benzamide ultra low volume liquids according to claim 1 is characterized in that: its application process is ultra low volume spraying, low-gallonage spraying or ultra low volume electrostatic spray.
CN 201110269980 2011-09-13 2011-09-13 Ultralow volume liquid containing chlorantraniliprole Active CN102379290B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201110269980 CN102379290B (en) 2011-09-13 2011-09-13 Ultralow volume liquid containing chlorantraniliprole

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201110269980 CN102379290B (en) 2011-09-13 2011-09-13 Ultralow volume liquid containing chlorantraniliprole

Publications (2)

Publication Number Publication Date
CN102379290A true CN102379290A (en) 2012-03-21
CN102379290B CN102379290B (en) 2013-09-11

Family

ID=45819446

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 201110269980 Active CN102379290B (en) 2011-09-13 2011-09-13 Ultralow volume liquid containing chlorantraniliprole

Country Status (1)

Country Link
CN (1) CN102379290B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103120184A (en) * 2012-06-01 2013-05-29 北京明德立达农业科技有限公司 Fosthiazate pesticide composition and application thereof
CN114007421A (en) * 2019-05-08 2022-02-01 拜耳公司 Absorption-promoting ULV formulations

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007123853A2 (en) * 2006-04-20 2007-11-01 E. I. Du Pont De Nemours And Company Five-membered heterocyclic invertebrate pest control agents
CN101743974A (en) * 2010-01-13 2010-06-23 海南大学 Propiconazole ultra-low volume preparation and preparation method thereof
CN101785455A (en) * 2010-02-05 2010-07-28 深圳诺普信农化股份有限公司 Pesticide oil suspension agent and preparation method thereof
CN102077829A (en) * 2011-03-03 2011-06-01 安徽农业大学 Efficient insecticidal bactericide containing R-diniconazole and chlorantraniliprole

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007123853A2 (en) * 2006-04-20 2007-11-01 E. I. Du Pont De Nemours And Company Five-membered heterocyclic invertebrate pest control agents
CN101743974A (en) * 2010-01-13 2010-06-23 海南大学 Propiconazole ultra-low volume preparation and preparation method thereof
CN101785455A (en) * 2010-02-05 2010-07-28 深圳诺普信农化股份有限公司 Pesticide oil suspension agent and preparation method thereof
CN102077829A (en) * 2011-03-03 2011-06-01 安徽农业大学 Efficient insecticidal bactericide containing R-diniconazole and chlorantraniliprole

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103120184A (en) * 2012-06-01 2013-05-29 北京明德立达农业科技有限公司 Fosthiazate pesticide composition and application thereof
CN114007421A (en) * 2019-05-08 2022-02-01 拜耳公司 Absorption-promoting ULV formulations

Also Published As

Publication number Publication date
CN102379290B (en) 2013-09-11

Similar Documents

Publication Publication Date Title
CN102349507B (en) Pymetrozine-containing ultralow volume liquid agent
CN102349503B (en) Ultra-low-capacity liquid containing imidaclothiz
CN102334500B (en) Insect-killing and disease-preventing suspension seed coating formulation
CN102273444A (en) Ultralow volume liquid containing thiamethoxam
CN101836641A (en) Oil-suspending agent disinfestation composition containing spinosyns and emamectin benzoate
CN102986700A (en) Insecticide composition containing flutenzine and bistrifluron
CN102972430A (en) Insecticidal composition containing thiamethoxam and acetamiprid
CN102379290B (en) Ultralow volume liquid containing chlorantraniliprole
CN103355301A (en) Pesticide composition containing pyridalyl
CN106954634A (en) A kind of composition pesticide and its application containing pyraclonil and anilofos
CN102265848B (en) Weeding composition containing bentazone, acifluorfen-sodium and haloxyfop-r-methyl, and application thereof
CN107258800A (en) A kind of composition pesticide containing avermectin B2a
CN101194621B (en) Mixed pesticide preparation of tubatoxin and butyl ether urea
CN104970036A (en) Novel suspended seed coating
CN108208015A (en) A kind of agricultural chemicals suspension agent and its preparation method and application
CN104094954A (en) Pesticide composition comprising ethoxysulfuron and halosulfuron-methyl and application thereof
CN107743967A (en) Composition pesticide and its application containing flumioxazin and flufenacet
CN106719760A (en) Herbicidal composition for rice field and its application
CN104904739A (en) Novel suspension seed coating agent
CN105076169A (en) Bactericidal composition containing albendazole and fludioxonil and application
CN103749529B (en) A kind of insecticidal and bactericidal composition
CN103704258B (en) A kind of Fungicidal insecticidal composition containing abietic acid ketone
CN108013065A (en) A kind of herbicide decrement control careless method of dispenser prevention and control transplanting rice at whole growth periods crop smothering
CN104604907A (en) Dicamba and pyributicarb herbicidal composition and application thereof
CN107114383A (en) It is a kind of containing pyraclonil He composition pesticide and its application of metamifop

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant