Dimethomorph uses-manufacture,factory,supplier from China

(Total 24 Products for Dimethomorph uses)
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: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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CAS: 110488-70-5MF: C21H22ClNO4MW: 387.86 Physical chemistry properties:The melting point of 125-149 ° CVapor pressure 1 x 10-6 Pa (25 °C)Sealed in dry,Room TemperatureWater solubility 50 mg L -1 (20-23 °C)  Toxicity:The acute oral LD50 of rats was greater than 3900 mg/kg, the transcutaneous LD50 was greater than 2000 mg/kg, and the acute inhaled LC50 of rats was greater than 4.24 mg/L.It has no irritation to rabbit skin, slight irritation to eyes, and no sensitization to guinea pigs.No mutagenic, teratogenic and carcinogenic effects were observed under the test conditions.
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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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Common name: MancozebChemical name: Coordination compound of 1,2-ethylenebisdithiocarbamate manganese and zinc ionMolecular formula: C4H8MnN2S4Zn Structural formula:Molecular weight: 332.71CAS No. : 8018-01-7Product description:The pure product of mancozeb is white powder, and the industrial product is off-white or light yellow powder with the smell of rotten eggs. It is hardly soluble in water, insoluble in most organic solvents, soluble in pyridine, and unstable to light, heat, and humidity.
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Product description:The pure made from mancozeb is white powder, and the commercial product is off-white or light yellow powder with the smell of rotten eggs. it's miles hardly ever soluble in water, insoluble in maximum natural solvents, soluble in pyridine, and volatile to mild, warmth, and humidity.
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Product description:Cypermethrin (cp) is a synthetic pyrethroid used as an insecticide in massive-scale business agricultural programs as well as in customer products for domestic functions. it behaves as a fast-performing neurotoxin in bugs. it is easily degraded on soil and plant life however can be effective for weeks while applied to indoor inert surfaces. exposure to daylight, water and oxygen will boost up its decomposition. cypermethrin is fairly toxic to fish, bees and aquatic insects, according to the countrywide pesticides telecommunications network (nptn).
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Thiamethoxam is a extensive-spectrum, systemic insecticide, which means that it's miles absorbed speedy with the resource of plant life and transported to all of its components, which includes pollen, in which it acts to discourage insect feeding.[citation needed] an insect can absorb it in its belly after feeding, or via direct contact, which includes thru its tracheal device.
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Common name: MesotrioneChemical name:2-[4-(methylsulfonyl)-2-nitrobenzoyl]-1,3-cyclohexanedioneMolecular formula: C14H13NO7SStructural formula:Molecular weight: 339.32CAS No. : 104206-82-8Product description:Mesotrione is an effective inhibitor of HPPD (4-hydroxyphenylpyruvate dioxidase), which is widely present in various organisms and catalyzes the initial reaction of plastoquinone and tocopherol biosynthesis.
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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: 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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Product description:it can kill mites and bugs, but now not eggs. the mechanism of movement is different from the overall insecticide is to intrude with neurophysiological sports, stimulate the discharge of γ -aminobutyric acid, and aminobutyric acid on arthropod nerve conduction inhibition. person mites, nymphs and insect larvae display paralysis after touch with avermectin, do not circulate or feed, and die in 2 ~ 4 days. the lethal effect of abamectin is slow as it does not cause speedy dehydration of insects.
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Product description:Bifenthrin is a pyrethroid insecticide. it's far extensively used towards ant infestations, consisting of the invasive pink fireplace ant, by influencing its frightened machine. it has a high toxicity to aquatic organisms.Bifenthrin is poorly soluble in water and often remains in soil. Its residual half-life in soil is between 7 days and 8 months, depending on the soil type, with a low mobility in most soil types. Bifenthrin has the longest known residual time in soil of insecticides currently on the market. It is a white, waxy solid with a faint sweet smell.
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Bifenthrin is a pyrethroid insecticide. it's miles extensively used in opposition to ant infestations, consisting of the invasive crimson fireplace ant, through influencing its apprehensive machine. it has a high toxicity to aquatic organisms.Bifenthrin is poorly soluble in water and often remains in soil. Its residual half-life in soil is between 7 days and 8 months, depending on the soil type, with a low mobility in most soil types. Bifenthrin has the longest known residual time in soil of insecticides currently on the market. It is a white, waxy solid with a faint sweet smell.
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Structural formula:Molecular weight: 422.9CAS No. : 82657-04-3Physical and chemical properties:Pure for gray solid. M.p. 68 ~ 70.6℃(industrial M.P. 61 ~ 66℃), relative density 1.210 (25℃), vapor pressure 2.4×10-5Pa, flash point 165℃Content,%≥ 95Product description:Bifenthrin is a pyrethroid insecticide. It is widely used against ant infestations, including the invasive red fire ant, by influencing its nervous system. It has a high toxicity to aquatic organisms.Bifenthrin is poorly soluble in water and often remains in soil.
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Structural formula:Molecular weight: 416.3CAS No. : 52315-07-8Product description:Cypermethrin (CP) is a synthetic pyrethroid used as an insecticide in large-scale commercial agricultural applications as well as in consumer products for domestic purposes. It behaves as a fast-acting neurotoxin in insects. It is easily degraded on soil and plants but can be effective for weeks when applied to indoor inert surfaces. Exposure to sunlight, water and oxygen will accelerate its decomposition.
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Chlorfenapyr is converted into active substances (insecticidal interest) by multifunctional oxidases in bugs. note: multifunctional oxidase mainly performs an critical role inside the interpretation of pyrethroids, organophosphorus and macrolides.Common name: CHLORFENAPYRChemical name:  4-bromo-2-(4-chlorophenyl)-1-ethoxymethyl-5-trifluoromethylpyrrole-3-carbonitrile Molecular formula: C15H11BrClF3N2OStructural formula:Molecular weight: 407.61CAS No. : 122453-73-0Physical and chemical properties:Pure white solid. M.p.
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Chlorfenapyr is converted into lively materials (insecticidal activity) via multifunctional oxidases in bugs. note: multifunctional oxidase mainly plays an important function in the interpretation of pyrethroids, organophosphorus and macrolides.Common name: CHLORFENAPYRChemical name:  4-bromo-2-(4-chlorophenyl)-1-ethoxymethyl-5-trifluoromethylpyrrole-3-carbonitrile Molecular formula: C15H11BrClF3N2OStructural formula:Molecular weight: 407.61CAS No. : 122453-73-0Physical and chemical properties:Pure white solid. M.p.
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Common name: AcetochlorChemical name: 2-chloro-N-(ethoxymethyl)-N-(2-ethyl-6-methylphenyl)acetamideMolecular formula:  C14H20ClNO2Structural formula:Molecular weight: 269.77CAS No. : 34256-82-1Physical and chemical properties:Light brown liquid. b.p.>200℃, m.p.>0℃, vapor pressure 133.3Pa, relative density 1.11 (30℃).
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Common name: 2,4-DChemical name:2,4-dichlorophenoxy-acetic acid; (2,4-dichlorophenoxy)acetic acid; Acetic acid, 2-(2,4-dichlorophenoxy)-Molecular formula: C8H6Cl2O3Structural formula: Molecular weight: 221.04CAS No. : 94-75-7Physical and chemical properties:White crystals. Melting point is 138°C, boiling point is 160°C (53Pa). Soluble in organic solvents such as ethanol, acetone, ether and benzene, but insoluble in water. Rat oral LD50375mg/kg.Usage:Used as plant growth regulator, antiseptic and fresh-keeping agent. It can be used in compatibility with other disinfectants.
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Common name: Clodinafop-propargylChemical name:2-propynyl-(R)-2-[4-(5-chloro-3-fluoro-2-pyridyloxy)phenoxyl]-prpionateMolecular formula: C17H13ClFNO4Structural formula: Molecular weight: 349.74CAS No.
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Common name: ClethodimChemical name: (5RS)-2-[(1EZ)-1-[(2E)-3-chloroallyloxyimino]propyl]-5-[(2RS)-2-(ethylthio)propyl]-3-hydroxycyclohex-2-en-1-oneMolecular formula: C17H26ClNO3SStructural formula:  Molecular weight: 359.91CAS No. : 99129-21-2Physical and chemical properties: The original medicine is amber transparent liquid.
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Common name: GlyphosateChemical name: N-(Phosphonomethyl)glycineMolecular formula: C3H8NO5PStructural formula:Molecular weight: 169.07CAS No. : 1071-83-6Physical and chemical properties:The pure product is a white solid. m.p.230℃ (decomposition). It is hardly soluble in general organic solvents; its solubility in water is 1.2% at 25°C. Usually made into glyphosate amine salt, such as isopropylamine salt, dimethylamine salt, etc., can also be made into sodium salt. The glyphosate salt is soluble in water.Product description:Glyphosate is an organophosphorus herbicide.
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Physical and chemical properties:The pure product is colorless crystal, m.p. 177~178℃ (decomposition), without difficulty soluble in dimethylformamide and chloroform; soluble in acetone, methanol, ethanol, ethyl acetate, dioxane; insoluble in water. stable to acid and alkali. business merchandise are light yellow crystals.Common name: Thiophanate-MethylChemical name: Dimethyl N,N′-[1,2-phenylenebis(azanediylcarbonothioyl)]dicarbamateMolecular formula: C12H14N4O4S2Structural formula:Molecular weight: 342.39CAS No.
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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.
Evaluation of human dietary exposure to glufosinate and its breakdown products by the EPA showed that the greatest risk from glufosinate was from contamination of drinking water. However, observed levels of exposure were found to be below levels of concern and were not considered a reasonable adverse health risk. Based on rodent studies, glufosinate is classified as not likely to be carcinogenic in humans.Glufosinate is a slight skin irritant and a severe eye irritant.
Glufosinate-ammonium is used for control of a wide range of annual and perennial broad-leaved weeds and grasses in fruit orchards, vineyards, rubber and oil palm plantations, ornamental trees and bushes, non-crop land, and pre-emergence in vegetables. Also used as a desiccant in potatoes, sunflowers, etc. For control of annual and perennial weeds and grasses in glufosinate-tolerant crops (oilseed rape, maize, soya beans, sugar beet) developed through gene technology. Applied at 0.4-1.5 kg/ha.
Amitraz is a triazapentadiene compound, a member of the amidine chemical family . It is a member of formammidine pesticides and is used worldwide . Amitraz is used as an insecticide/acaricide for controling the ectoparasites in animals . Commercial formulations of amitraz generally contain 12.5-20% of the drug in organic solvents, especially Xylene, which is also used as a solvent in paints, cleaners, and glues.Adverse reaction and side effects have been reported in animals exposed to the product, but only a limited number of human intoxication cases have been published in the literature.
The registration for the insecticide Ohkami (Tolfenpyrad), from Sipcam Nichino, was extended to 11 more crops in Brazil to manage a pest that is difficult to control: the cruciferous moth (Plutella xylostella).According to the manufacturer, the product had already reached representative levels of commercialization and showed proven effectiveness in controlling the tomato leafminer (Tuta absoluta).The agronomist Eric Ono, a researcher at Sipcam Nichino, says the cruciferous moth feeds on ‘brassic’ leaves such as broccoli, cabbage, cauliflower, kale, and others.
The technology company Indigo announced the official launch of its first crop protection product: the biotrinsic bionematicide, formulated based on Pseudomonas oryzihabitans.The novelty was presented during the Tecnoshow 2023 fair, which had special coverage by AgroPages.According to Indigo, biotrinsic has a ″premium performance, controlling all stages of nematode growth and leaving plants and soil healthier.″The main targets are cysts (Heterodra glycines), galls (Meloidogyne incognita), and lesions (Pratylenchus brachyurus).″Since it is a multi-crop bionematicide, it can be applied to so
Terramera has launched its latest product, a new biological pesticide that provides insect, mite, and disease management in a single application for both organic and conventional growers in the United States.  A powerful new tool for row crop growers, SOCORO is labeled for use as a standalone, a tank mix partner or in a program rotation. SOCORO can be applied in-furrow or foliar targeting problematic pests in key commodity crops including grains, legumes, and oil seed.  SOCORO is safe choice for growers with a re-entry interval of 4 hours and a zero-day preharvest interval.
Acetamiprid is an organic compound with the chemical formula C10H11ClN4. It is an odorless neonicotinoid insecticide produced under the trade names Assail, and Chipco by Aventis CropSciences. It is systemic and intended to control sucking insects (Thysanoptera, Hemiptera, mainly aphids) on crops such as leafy vegetables, citrus fruits, pome fruits, grapes, cotton, cole crops, and ornamental plants.
Glufosinate movement in soil depends on both soil properties and pesticides properties. The leaching potential of glufosinate is reduced with increasing soil clay and organic matter content.
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.