190604-92-3 Usage
Description
Acetamidiprid-n-desmethyl, also known as N-(6-chloro-3-pyridylmethyl)-N'-cyano-acetamidine, is an active metabolite of acetamiprid, a widely used neonicotinoid insecticide. It is characterized by its potent insecticidal and neuroblocking activities in animals, making it a significant compound in the field of pest control.
Uses
Used in Pest Control Industry:
Acetamidiprid-n-desmethyl is used as an insecticide for its potent insecticidal and neuroblocking activities. It is particularly effective against a variety of pests, including aphids, whiteflies, and thrips, which are known to cause significant damage to crops. The compound works by targeting the nicotinic acetylcholine receptors in the central nervous system of insects, leading to paralysis and eventual death.
Additionally, acetamiprid-n-desmethyl is used as a neuroblocker in the study and understanding of the nervous system in animals. Its ability to target and modulate the activity of nicotinic acetylcholine receptors makes it a valuable tool in research related to neurophysiology and the development of new treatments for neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 190604-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,6,0 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 190604-92:
(8*1)+(7*9)+(6*0)+(5*6)+(4*0)+(3*4)+(2*9)+(1*2)=133
133 % 10 = 3
So 190604-92-3 is a valid CAS Registry Number.
190604-92-3Relevant articles and documents
Reaction kinetics and mechanisms of neonicotinoid pesticides with sulfate radicals
Dell'Arciprete, Maria L.,Cobos, Carlos J.,Martire, Daniel O.,Furlong, Jorge P.,Gonzalez, Monica C.
, p. 672 - 680 (2011)
The reaction kinetics and mechanisms of three neonicotinoid insecticides, imidacloprid (IMD), thiacloprid (THIA) and acetamiprid (ACT) with sulfate radicals were studied by flash-photolysis of peroxodisulfate, S 2O82-. The absolute rate constants (3 ± 1) × 108, (1.1 ± 0.6) × 109, and (3 ± 1) × 109 M-1 s-1 were determined for IMD, ACT, and THIA, respectively. The reactivity and absorption spectra of the observed organic intermediates are in line with those reported for α-aminoalkyl radicals, and their absorption spectra agree very well with those estimated employing the time-dependent density functional theory with explicit account for bulk solvent effects. The mono- and di-hydroxylated oxidation products of the insecticides were identified as primary degradation products. The proposed reaction mechanism supports an initial charge transfer from the amidine nitrogen of the insecticides to the sulfate radicals. The pyridine moiety of the insecticides remains unaffected even after long irradiation times, until nicotinic acid is formed.
