Azoxystrobin Mode of Action-manufacture,factory,supplier from China

(Total 24 Products for Azoxystrobin Mode of Action)
Alachlor is an herbicide from the chloroacetanilide family. It is an odorless, white solid. The greatest use of alachlor is for control of annual grasses and broadleaf weeds in crops. Use of alachlor is illegal in the European Union and no products containing alachlor are currently registered in the United States.Its mode of action is elongase inhibition, and inhibition of geranylgeranyl pyrophosphate (GGPP) cyclisation enzymes, part of the gibberellin pathway. Common name: AlachlorChemical name:  2-chloro-N-(2,6-diethylphenyl)-N-(methoxymethyl)acetamide; Molecula
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MF: C22H17N3O5MW: 403.39CAS: 131860-33-8 Physical and chemical properties:Density: 1.33 g/cm3Melting point: 118-119 ℃Boiling point: 581.3 ℃Flash: 305.3 ℃Appearance: white crystalline powderUsage :because of its prevention and cure of bacteria ester disease range is wide, suitable for wheat, corn, rice and other food crops, peanut, sesame, tobacco, cotton and other economic crops, tomato, watermelon, cucumber, eggplant, chili, vegetable crops, such as apple, pear, kiwi fruit, mango, litchi, longan, banana and other fruit trees, medicinal herbs, flowers, such as hundreds of crops.Its e
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Common name: AvermectinChemical name:abamectin (combination of avermectin B1a and avermectin B1b) Molecular formula: C49H74O14Structural formula: Molecular weight: 887.11CAS No. : 71751-41-2Product description:It can kill mites and insects, but not eggs. The mechanism of action is different from the general insecticide is to interfere with neurophysiological activities, stimulate the release of γ -aminobutyric acid, and aminobutyric acid on arthropod nerve conduction inhibition.
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Usage:Azoxystrobin is a xylem-cellular systemic fungicide with translaminar, protectant and healing homes. in cereal crops, its fundamental outlet, the duration of ailment control is normally approximately 4 to 6 weeks all through the period of energetic stem elongation. all insecticides are required to seek registration from suitable authorities within the country in which they may be used.
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Common name: AzoxystrobinChemical name: Methyl(2E)-2-(2-{[6-(2-cyanophenoxy)pyrimidin-4-yl]oxy}phenyl)-3-methoxyprop-2-enoateMolecular formula: C22H17N3O5Structural formula: Molecular weight: 403.39CAS No. : 131860-33-8Physical and chemical properties:Appearance White crystalline solidUsage:Azoxystrobin is a xylem-mobile systemic fungicide with translaminar, protectant and curative properties. In cereal crops, its main outlet, the length of disease control is generally about four to six weeks during the period of active stem elongation.
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Product description:Fenvalerate is a synthetic pyrethroid insecticide. it is a aggregate of 4 optical isomers that have one-of-a-kind insecticidal sports. the 2-s alpha (or ss) configuration, referred to as esfenvalerate, is the maximum insecticidally lively isomer. fenvalerate includes about 23% of this isomer.Fenvalerate is an insecticide of moderate mammalian toxicity. In laboratory animals, central nervous system toxicity is observed following acute or short-term exposure.
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Product description:Z-cis-cyfluthrin is an intermediate for the preparation of lambda-cyhalothrin (cyfluthrin), tefluthrin, bifenthrin and other pyrethroids.Utilization:The lambda cyhalothrin acid fluorine-containing intermediate is one of the varieties of chrysanthemum acid, that is an essential intermediate for the synthesis of pyrethroid insecticides.
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Fibulonil can result in cl- float by way of blocking off the cl- channel of the nerve membrane managed by way of γ -aminobutyric acid receptor, which causes excessive excitement of the apprehensive gadget and results in the dying of the insect frame, as a result attaining the prevention and manipulate impact of various monetary pests.Common name: FIPRONILChemical name: 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrileMolecular formula: C12H4Cl2F6N4OSStructural formula: Molecular weight: 437.15CAS No.
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Common name: TebuconazoleChemical name:1-(4-Chlorophenyl)-4,4-dimethyl-3-(1,2,4-triazole-1-yl-methyl)pentane-3-olMolecular formula: C16H22ClN3OStructural formula: Molecular weight: 307.82CAS No. : 80443-41-0Product description:Tebuconazole is a kind of high efficiency, broad spectrum, internal absorption triazole bactericidal pesticide, with three functions of protection, treatment, eradication, wide bactericidal spectrum, long duration of efficacy. It was found that tebuconazole, like all triazole fungicides, could inhibit the biosynthesis of ergosterol from fungicide.
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Common name: DimethomorphChemical name:(E,Z)4-[3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)acryloyl] morpholineMolecular formula: C21H22ClNO4Structural formula:Molecular weight: 387.86CAS No. : 110488-70-5Product description:It is a special fungicide of the class of oomycetes. Its function is to destroy the formation of cell wall membrane. It has an effect on all stages of the life history of oomycetes. It is especially sensitive in the formation stage of sporangia stems and oospores, at very low concentrations. Down (<0.25μg/ml) is inhibited.
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Product description:emamectinbenzoate, emamectinbenzoate for brief, it is the result of the derivatization observe on the hydroxyl institution of four "-(α -1-zetan fructose-organization)-α -1-zetan fructose with the aid of merck in 1984.
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Product description:It is a unique fungicide of the elegance of oomycetes. its function is to spoil the formation of cellular wall membrane. it has an effect on all tiers of the existence history of oomycetes. it's far in particular sensitive in the formation stage of sporangia stems and oospores, at very low concentrations. down (<0.25μg/ml) is inhibited. no move-resistance to phenylamides.Common name: DimethomorphChemical name:(E,Z)4-[3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)acryloyl] morpholineMolecular formula: C21H22ClNO4Structural formula:Molecular weight: 387.86CAS No.
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Product description:Imidacloprid is a systemic insecticide belonging to a category of chemicals referred to as the neonicotinoids which act on the significant apprehensive system of bugs. the chemical works via interfering with the transmission of stimuli in the insect nervous machine. in particular, it causes a blockage of the nicotinergic neuronal pathway. by blockading nicotinic acetylcholine receptors, imidacloprid prevents acetylcholine from transmitting impulses between nerves, ensuing inside the insect's paralysis and eventual death.
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Product description:Propolachlor, also referred to as saufort, is mainly used for directly sown rice fields. it has the traits of secure rice boom, extensive weed control spectrum and proper weed manage impact. it could essentially manipulate the damage of weeds in the whole boom length.
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Product description:Tebuconazole is a sort of high performance, large spectrum, inner absorption triazole bactericidal pesticide, with three capabilities of safety, remedy, eradication, huge bactericidal spectrum, long length of efficacy. it became located that tebuconazole, like several triazole fungicides, could inhibit the biosynthesis of ergosterol from fungicide. tebuconazole is used as seed treatment agent and foliar spray all over the global. it has a extensive bactericidal spectrum, excessive activity and long length of efficacy.
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Structural formula:Deltamethrin is a pyrethroid composed of a single stereoisomer, of a possible 8 stereoisomers, selectively prepared by using the esterification of (1r,3r)- or cis-2,2-dimethyl-3-(2,2-dibromovinyl)cyclopropanecarboxylic acid with (alpha,s)- or (+)-alpha-cyano-three-phenoxybenzyl alcohol or by way of selective recrystallization of the racemic esters acquired by esterification of the (1r,3r)- or cis-acid with the racemic or (alpha-r, alpha-s, or alpha-r/s)- or + or − alcohol.Molecular weight: 505.2CAS No.
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Common name: EpoxiconazoleChemical name:1-[[3-(2-chlorophenyl)-2-(4-fluorophenyl)oxiran-2-yl]methyl]-1,2,4-triazole Molecular formula: C17H13ClFN3OStructural formula: Molecular weight: 329.76CAS No. : 135319-73-2Product description: Epoxiconazole is a fungicide active ingredient from the class of azoles developed to protect crops. In particular, the substance inhibits the metabolism of fungi cells infesting useful plants, and thereby prevents the growth of the mycelia (fungal cells). Epoxiconazole also limits the production of conidia (mitospores).
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Common name: BETA-CYPERMETHRINChemical name: Cyano(3-phenoxyphenyl)methyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylateMF: C22H19Cl2NO3MW: 416.29716CAS: 86752-99-0Structural formula:  Product description: Beta-cypermethrin is a pyrethroid pesticide, which is a kind of synthetic pesticide similar to natural pyrethrin in structure. Its molecule is composed of two parts: inulin and alcohol.Beta-cypermethrin is used to control agricultural pests by touching and gastric toxicity.
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Product description:Prochloraz, also referred to as promethazine, promethazine, shibaoke, and prochloraz, is an imidazole enormous-spectrum pesticide fungicide, which acts via inhibiting the biosynthesis of sterols. even though it does not have a systemic effect, it has sure conductivity residences. it has apparent control impact on diverse plant life because of ascomycetes and semi-chemicalbook micro organism. it may moreover be mixed with most fungicides, insecticides, and herbicides, and has appropriate manage consequences.
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Common name:  GlufosinateChemical name: 2-Amino-4-[hydroxy(methylphosphonoyl)]butanoic acidMolecular formula: C5H18N3O4PStructural formula:Molecular weight: 215.19CAS No. : 77182-82-2Product description:Glufosinate-ammonium, also known as glufosinate, is a non-selective foliar spray of organophosphorus herbicide. It was first synthesized and developed by the Federal German Hoechst Chemical Company in 1979.
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Chemical name of Indoxacarb products:methyl 7-chloro-2-[methoxycarbonyl-[4-(trifluoromethoxy)phenyl]carbamoyl]-3,5-dihydroindeno[1,2-e][1,3,4]oxadiazine-4a-carboxylate;Physical and chemical properties of Indoxacarb products:Molecular weight : 527.834Density: 1.53Melting point: 139-141 DHS CBoiling point: 571.4ºC at 760 mmHgFlash: DHS 299.3 CMolecular  formula :C22H17ClF3N3O7Toxicity of Indoxacarb products(DAPX-MP062) acute transoral: LD50: male 1730mg/kg, female 268mg/kg: rabbit acute transcutaneous LD50: & GT; 5000 mg/kg.
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Usage:Chlorpyrifos is used in approximately one hundred nations round the world to manipulate insects in agricultural, residential, and business settings. its use in residential packages is limited in more than one international locations. in step with dow, chlorpyrifos is registered for use in nearly one hundred nations and is yearly carried out to approximately eight.five million crop acres. the crops with the maximum use consist of cotton, corn, almonds, and fruit trees, consisting of oranges, bananas, and apples.
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Product description:Difenoconazole, also referred to as oxadifenazole, is a triazole fungicide and a sterol demethylation inhibitor. it has the characteristics of high performance, wide spectrum, low toxicity, and low dosage. an incredible kind of triazole fungicides with strong systemic houses. by using inhibiting the biosynthesis of ergosterol in pathogenic cells, it destroys the structure and characteristic of pathogen cell membranes. it is used in fruit trees, chemicalbook greens, wheat, potatoes, beans, melons, and so on.
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Product description:Kresoxim-methyl is a exceptionally powerful, wide-spectrum, new fungicide. it has an amazing control effect on strawberry powdery mold, melon powdery mold, cucumber powdery mould, pear scab and different sicknesses. it can manipulate and deal with maximum sicknesses inclusive of ascomycetes, basidiomycetes, deuteromycetes and oomycetes. it has a sturdy inhibitory effect at the germination of spores and the increase of mycelium in leaves, and has defensive, healing and removing activities.
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Relate News
The carboxylic acid amide (CAA) fungicides especially manage foliar Oomycetes illnesses, consisting of downy mould and overdue blight via way of means of inhibition of Cellulose synthase. This bankruptcy discusses the history, synthesis, mode of action, organic interest, and the structure-interest courting of CAA fungicides. The unique fungicidal interest of dimethomorph (1) in opposition to Oomycetes illnesses changed into found at some stage in the 1980s.
Azoxystrobin has a wide fungicidal spectrum and is soluble in various solvents such as methanol and acetonitrile, in addition to emulsifiable oils, and has good activity against almost all pathogens of the fungal world.
Azoxystrobin is still very effective against those strains of fungicides that have been used frequently with reduced susceptibility. This fungicide enhances plant resistance, promotes crop growth, has the effect of delaying aging, increasing photosynthesis, and improving crop quality and yield, and is a high-quality good fungicide. Azoxystrobin has good control effect on powdery mildew on wheat spike and high prevention effect on sudden eye spot disease caused by filamentous fungus genus.
Fenpropathrin, or fenopropathrin, is a broadly used pyrethroid insecticide in agriculture and household. Fenpropathrin is an ingestion and get in touch with artificial pyrethroid. Its mode of movement is similar to other natural (pyrethrum) and artificial pyrethroids where in they interfere with the kinetics of voltage gated sodium channels causing paralysis and death of the pest. Fenpropathrin was the primary of the light-stable artificial pyrethroids to be synthesized in 1971, however it was not commercialized till 1980.
Metaldehyde acts directly and specifically on the mucous producing cells found only in slugs and snails. This action is irreversible and results in the death of the animal. Metaldehyde causes the mucous cells to secrete large amounts of mucous, therefore depleting their energy reserves by ultimately exhausting them. This happens irrespective of the temperature or the amount of moisture in the local environment.
Lambda-Cyhalothrin Used as an Insecticide in Agriculture. Inhibit the conduction of the nerve axon of insects, have the effect of avoiding, knocking down and poisoning insects. It has a wide insecticidal spectrum, high activity and rapid efficacy. It is resistant to rain washing after spraying, but it is easy to develop resistance to it after long-term use , It has a certain control effect on pests and mites of piercing and sucking mouthparts, and the mechanism of action is the same as that of fenvalerate and cyfluthrin. The difference is that it has a good inhibitory effect on mites.
Pyridine-based ring systems are one of the most extensively used heterocycles in the field of drug design, primarily due to their profound effect on pharmacological activity, which has led to the discovery of numerous broad-spectrum therapeutic agents.
The European Commission announced the extension of the approval periods of some pesticide active substances.According to the Commission, due to the fact that the assessment of those active substances has been delayed for reasons beyond the control of the applicants, the approvals of those active substances are likely to expire before a decision has been taken on their renewal.
1. Widely used in insect mite control of fruit trees, cotton, vegetables, tea and other crops2. Broad spectrum, high efficiency pyrethroid insecticide and acaricide, with touching and repellent effect, can control lepidoptera, hemiptera and mite pests of vegetables, cotton, cereal crops.3. High efficiency, broad spectrum pyrethroids, with tactile and repellent effects, as well as gastric toxicity. In addition to the general properties of pyrethrin synthesis, it has a good effect on a variety of crops, so it has the advantages of mite removal.
Thiamethoxam is a systemic insecticide in the class of neonicotinoids. It has a broad spectrum of activity against many types of insects. Thiamethoxam can be used as a seed dresser.Thiamethoxam is a broad-spectrum, systemic insecticide, which means it is absorbed quickly by plants and transported to all of its parts, including pollen, where it acts to deter insect feeding.[citation needed] An insect can absorb it in its stomach after feeding, or through direct contact, including through its tracheal system.