• Agrochemical Pesticide Insecticide Imidacloprid
  • Agrochemical Pesticide Insecticide Imidacloprid

Agrochemical Pesticide Insecticide Imidacloprid

Appearance: Powder
Source: Organic Synthesis
Toxicity of High and Low: Highly Toxic and High Toxic Drugs
Mode: Systemic Insecticide
Toxicological Effect: Nerve Poison
Transport Package: 25kg/Drum
Samples:
US$ 100/kg 1 kg(Min.Order)
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Basic Info.

Model NO.
SV015
Specification
95%TC, 70% WDG, 70% WP, 10% SL
Trademark
SINOVID
Origin
China
HS Code
2933399026
Production Capacity
5000kg/Month

Product Description

Agrochemical Pesticide Insecticide Imidacloprid

Agrochemical Pesticide Insecticide Imidacloprid
 
Common Name
Imidacloprid
 
IUPAC
(E)-1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine
 
CAS
(2E)-1-[(6-chloro-3-pyridinyl)methyl]-N-nitro-2-imidazolidinimine
 
CAS No.
138261-41-3
 
Molecular Formula
C9H10ClN5O2
 
Molecular Structure
 
 
 
General Product Information
 
 
Category
Insecticides > Neonicotinoid insecticides
 
Activity
Insecticide
Imidacloprid acts by contact and ingestion as an antagonist of the post-synaptic nicotinic receptors in the insect central nervous system, blocking acetylcholine at the post-synaptic membrane and impairing normal nerve function. The target pest's feeding activity ceases within minutes to hours and death usually occurs between 1-7 days depending on mode of application.

The compound has a systemic translaminar activity and is readily absorbed from the roots and distributed acropetally. This property is an important pre-requisite for soil applications such as in-furrow, granular, seed treatment and seedling-box applications in rice. Imidacloprid shows high selectivity, quick knock-down effect and long residual activity. It is effective against adult and larval stages of sucking and biting insects, soil insects and termites but has no effect on nematodes and spiders.

Since the first launch of imidacloprid, with consideration of new neonicotinoid insecticides entering the market, Bayer has issued guidelines to prevent the resistance and cross-resistance development based on baseline susceptibility and cross-resistance studies. Several studies have shown no cross-resistance with other insecticides but the monitoring of critical field populations worldwide is ongoing.

Trials in Bangladesh in 2000/1 (IPPC, 2004) on cotton showed that imidacloprid gave up to 70% control of aphids and jassids 75 days after sowing at an application rate of 4.5 g/kg seed. 3.5 and 2.5 g/kg seed gave around 60% and 65% control, respectively. Imidacloprid gave high levels of control of whitefly (Trialeurodes vaporariorum) in trials on greenhouse strawberries in California (IPPC, 2004).
 
CropUse
CropUses: 
apples, aubergines, barley, beans, beets, berries, cereals, cilantro, citrus, cole crops, cotton, cranberries, cucumbers, cucurbits, currants, fodder beets, garden flowers, grapes, greenhouse crops, hops, lawns, legumes, lettuce, lupins, mangos, maize, melons, mustard, nurseries, oats, oilseed rape (canola), ornamentals, pasture, pecans, peppers, pome fruits, potatoes, rice, rye, snap beans, sorghum, spinach, stone fruits, strawberries, sugar beets, sunflowers, sweet corn, tobacco, tomatillos, tomatoes, triticale, tropical fruits, turf, vegetables, watercress, wheat 
 

178.5 g ai/ha (maximum rate, Admire)

 

90 g ai/ seed unit (seed treatment)

 

 
Pest Spectrum
control of sucking pests (Jassids, white fly, thrips, aphids , BPH  and other soil pest).
 
Formulation
AE = Aerosol dispenser
DP = Dustable powder
FS = Flowable concentrate for seed treatment
GR = Granule
SL = Soluble concentrate
SC = Suspension concentrate (=flowable concentrate)
 
Premix
Imidacloprid+beta-cyfluthrin
Imidacloprid+lambda-cyhalothrin
Imidacloprid+abamectin
Imidacloprid+acephate
Imidacloprid+bifenthrin
Imidacloprid+buprofezin
Imidacloprid+captan+carboxin
Imidacloprid+carbosulfan+zeta-cypermethrin
Imidacloprid+carboxin+metalaxyl
Imidacloprid+chlorpyrifos
Imidacloprid+cyfluthrin
Imidacloprid+imazalil+metalaxyl+tebuconazole
Imidacloprid+ipconazole+metalaxyl
Imidacloprid+mancozeb
Imidacloprid+mancozeb+thiophanate-methyl
Imidacloprid+metalaxyl
Imidacloprid+metalaxyl+tebuconazole
Imidacloprid+pyridaben
Imidacloprid+thiodicarb
Imidacloprid+thiram
Imidacloprid+esfenvalerate
Imidacloprid+dichlorvos
Imidacloprid+carbosulfan
Imidacloprid+carbendazim
Imidacloprid+carbendazim+thiram
Imidacloprid+carbendazim+triadimefon
Imidacloprid+carbendazim+carboxin
Imidacloprid+thiram+carboxin
Imidacloprid+thiram+tebuconazole
Imidacloprid+beta-cypermethrin
Imidacloprid+fenpropathrin
Imidacloprid+validamycin
Imidacloprid+validamycin+thiosultap-monosodium
Imidacloprid+pirimicarb
Imidacloprid+dimethoate
Imidacloprid+cypermethrin
Imidacloprid+prochloraz
Imidacloprid+methomyl
Imidacloprid+fenvalerate
Imidacloprid+triazophos
Imidacloprid+triadimefon
Imidacloprid+azocyclotin
Imidacloprid+thiosultap-diammonium
Imidacloprid+thiosultap-monosodium
Imidacloprid+thiosultap-disodium
Imidacloprid+isocarbophos
Imidacloprid+bacillus thuringiensis
Imidacloprid+tebuconazole
Imidacloprid+phoxim
Imidacloprid+omethoate
Imidacloprid+isoprocarb
Imidacloprid+indoxacarb
Imidacloprid+fenobucarb
Imidacloprid+deltamethrin
Imidacloprid+fipronil
Imidacloprid+Fludioxonil+Difenoconazole
tebuconazole+prothioconazole+metalaxyl+imidacloprid
bifenthrin+zeta-cypermethrin+imidacloprid
Spirotetramat+Imidacloprid
fluopyram+imidacloprid
MOXIDECTIN+IMIDACLOPRID

Premix Parters: Bacillus licheniformis bifenthrin cytokinins cytokinins gibberellic acid cytokinins 1-naphthaleneacetic acid gibberellic acid

 
 
Physical & Safety Data
 
 
Physical Properties
Molecular weight:255.7; Physical form:Colourless crystals, with a weak characteristic odour. Density:1.54 (23 °C); Melting point:144 °C; Vapour pressure:4 × 10-7 mPa (20 °C); 9 × 10-7 mPa (25 °C); Henry constant:2 × 10-10 Pa m3 mol-1 (20 °C, calc.); Partition coefficient(n-octanol and water):logP = 0.57 (21 °C); Solubility:In water 0.61 g/l (20 °C). In dichloromethane 55, isopropanol 1.2, toluene 0.68, n-hexane <0.1 (all in g/l, 20 °C).; Stability:Stable to hydrolysis at pH 5-11.
 
Toxicology
Oral:Acute oral LD50 for male and female rats c. 450 mg/ kg. Percutaneous:Acute percutaneous LD50 (24 h) for rats >5000 mg/kg. Non-irritating to eyes and skin (rabbits). Not a skin sensitiser. Inhalation: LC50 (4 h) for rats >5323 mg/m3 dust, 69 mg/m3 air (aerosol). ADI:0.0085 mg/ kg.
 
Environmental Profile

Ecotoxicology: 
Algae: ErC50 for Pseudokirchneriella subcapitata >100 mg/l.Bees:Harmful to honeybees by direct contact, but no problems expected when not sprayed into flowering crop or when used as a seed treatment.Birds:Acute oral LD50 for Japanese quail 31, bobwhite quail 152 mg/kg. Dietary LC50 (5 d) for bobwhite quail 2225, mallard ducks >5000 mg/ kg.Daphnia: LC50 (48 h) 85 mg/l.Fish: LC50 (96 h) for golden orfe 237, rainbow trout 211 mg/l.Worms: LC50 for Eisenia foetida 10.7 mg/ kg dry soil. 

Environmental fate: 
Imidacloprid is highly toxic to honeybees by direct contact and harmful to insects in general, including predatory insects such as ladybirds and lacewings. Imidacloprid is slightly toxic to juvenile and adult fish and to aquatic invertebrates. The product appears to repel birds when used as a seed treatment.

Fate in soil: 
Imidacloprid displays a medium absorption to soil and some degree of mobility, although leaching into deeper soil layers is not to be expected. In soil, imidacloprid is degraded continuously but not very rapidly; the product does not accumulate and is not persistent and the maximum concentrations in soil during long-term trials under unfavourable conditions reached a plateau level and declined in the absence of further applications. Imidacloprid has a half-life of 27 days in silt loam sediment under anaerobic conditions. Upon exposure to light, imidacloprid had a half-life of 39 days on sandy loam soil and the product is stable to hydrolysis at acid-neutral Ph under exclusion of light. The main routes of degradation of imidacloprid are photodegradation and microbial activity.

Fate in aquatic systems: 
Imidacloprid degrades readily in the presence of light and the product rapidly undergoes degradation in water via photolytic reactions or microbial activity. Upon exposure to light, imidacloprid has a half-life of one hour in water.

 
Transport Information
Signal Word:CAUTION; Hazard Class:II(Moderately hazardous

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Manufacturer/Factory, Trading Company
Registered Capital
1000000 RMB
Plant Area
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