Customization: | Available |
---|---|
CAS No.: | 138261-41-3 |
Formula: | C9H10ClN5O2 |
Still deciding? Get samples of US$ 1/Piece
Request Sample
|
Suppliers with verified business licenses
Audited by an independent third-party inspection agency
Product Information
Imidacloprid is a systemic, chloro-nicotinyl insecticide with soil, seed and foliar uses for the control of sucking insects including rice hoppers, aphids, thrips, whiteflies, termites, turf insects, soil insects and some beetles.
It is most commonly used on rice, cereal, maize, potatoes, vegetables, sugar beets, fruit, cotton, hops and turf, and is especially systemic when used as a seed or soil treatment.
Category : |
Insecticide |
|||||||||||||||||||||||||||||||||||||||||||
CAS NO : | 138261-41-3 | |||||||||||||||||||||||||||||||||||||||||||
EC NO : | ||||||||||||||||||||||||||||||||||||||||||||
MF : | C9H10ClN5O2 | |||||||||||||||||||||||||||||||||||||||||||
MW : | 255.661 | |||||||||||||||||||||||||||||||||||||||||||
Specification : | 95%TC, 70%WDG, 70%WP, 70%WS, 35%SC,25%WP,20%SL,10%WP,60%FS | |||||||||||||||||||||||||||||||||||||||||||
Product description : |
|
|||||||||||||||||||||||||||||||||||||||||||
Synonyms : | 1-((6-Chloro-3-pyridinyl)methyl)-N-nitro-imidazolidinimine;((6-Chloro-3-pyridinyl)methyl)-N-nitro-2-imidazolidinimine,96% imidacloprid TC;1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine;1-[(6-chloro-3-pyridinyl)methyl]-N-nitro-2-imidazolidinimine;(EZ)-1-(6-Chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine;1-((6-chloro-3-pyridinyl)methyl)-4,5-dihydro-N-nitro-1H-imidazol-2-amine;1-((6-Chloro-3-pyridinyl)methyl)-4,5-dihydro-N-nitro-imidazol-2-amine;Admire;Confidor;Gaucho;Merit;NTN33823;NTN 33893;NTN-33893;1-(6-chloro-3-pyridymethyl)-N-nitromidazolidin-2-ylideneamine;1-[(6-chloropyridin-3-yl)methyl]-N-nitro-4,5-dihydro-1H-imidazol-2-amine;1-[(6-chloropyridin-3-yl)methyl]-3-nitroimidazolidin-2-imine;Imidaclopride; | |||||||||||||||||||||||||||||||||||||||||||
Molecular Structure : |
Imidacloprid works by interfering with the transmission of stimuli in the insect nervous system. Specifically, it causes a blockage in a type of neuronal pathway (nicotinergic) that is more abundant in insects than in warm-blooded animals (making the chemical selectively more toxic to insects than warm-blooded animals).
This blockage leads to the accumulation of acetylcholine, an important neurotransmitter, resulting in the insect's paralysis, and eventually death.
It is effective on contact and via stomach action. Imidacloprid can be phytotoxic (toxic to plants) if not used according to manufacturers instructions, and it has a tendency to reduce seedling emergence and crop vigour.