| Weight | 255.665 g/mol |
|---|---|
| Formula | C9H10ClN5O2 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Imidacloprid (138261-41-3, 105827-78-9)
Score:
#184 in Biology
,
#191 in Chemistry
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- A nicotinic acetylcholine receptor mutation conferring target-site resistance to imidacloprid in Nilaparvata lugens (brown planthopper) (Proceedings of the National Academy of Sciences of the United States of America, 2005)
- Actions of imidacloprid and a related nitromethylene on cholinergic receptors of an identified insect motor neurone (Pesticide Science, 1991)
- Discrepancy between acute and chronic toxicity induced by imidacloprid and its metabolites in Apis mellifera (Environmental Toxicology and Chemistry, 2001)
- Baseline determination and detection of resistance to imidacloprid in Bemisia tabaci (Homoptera: Aleyrodidae) (Bulletin of Entomological Research, 1996)
- Effects of imidacloprid and deltamethrin on associative learning in honeybees under semi-field and laboratory conditions (Ecotoxicology and Environmental Safety, 2004)
- Over-expression of cytochrome P450 CYP6CM1 is associated with high resistance to imidacloprid in the B and Q biotypes of Bemisia tabaci (Hemiptera: Aleyrodidae). (Insect Biochemistry and Molecular Biology, 2008)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H402: Harmful to aquatic life
- H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
SMILESC1CN(C(=N1)N[N+](=O)[O-])CC2=CN=C(C=C2)Cl
-
InChIKeyYWTYJOPNNQFBPC-UHFFFAOYSA-N
- Pubchem - Imidacloprid
- Wikipedia - imidacloprid
Imidacloprid is a systemic insecticide that acts as an insect neurotoxin and belongs to a class of chemicals called the neonicotinoids which act on the central nervous system of insects, with much lower toxicity to mammals. The chemical works by interfering with the transmission of stimuli in the insect nervous system. Specifically, it causes a blockage of the nicotinergic neuronal pathway.
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+
101990-44-7
(Imine formation from aldehyde)
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