aminocarb
Sign in to saveAnimocarb (Matacil) is an organic chemical compound with the molecular formula C11H16N2O2. It has a colorless or white crystal-like appearance and is most commonly used as an insecticide.
Research
60 papers- Aminocarb Exposure Induces Cytotoxicity and Endoplasmic Reticulum Stress-Mediated Apoptosis in Mouse Sustentacular Sertoli Cells: Implications for Male Infertility and Environmental Health.Biology · 2024
- Hemoglobin targeting potential of aminocarb pesticide: Investigation into dynamics, conformational stability, and energetics in solvent environment.Biochemical and biophysical research communications · 2024
- Exploration of the structure and interactions of 4-(dimethylamino)-3-methylphenyl N-methylcarbamate (Aminocarb).Acta crystallographica. Section C, Structural chemistry · 2025
- Concentration-dependent biphasic toxicity and steroidogenic stimulation by aminocarb in murine Leydig cells.Environmental toxicology and pharmacology · 2025
- Immunotoxicity of aminocarb. III. Exposure route-dependent immunomodulation by aminocarb in mice.Toxicology · 1995
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 208.121177752
- Has use
- insecticide
Show 3 more facts
- canonical SMILES
- CC1=C(C=CC(=C1)OC(=O)NC)N(C)C
- Commons category
- Aminocarb
- chemical formula
- C₁₁H₁₆N₂O₂
Sources (2)
via Wikidata · CC0
~3 min read
Encyclopedic overview
7 sectionsContents
- History
- Production and uses
- Reactions
- Irradiation
- Hydrolysis
- Biomedical effects
- References
Animocarb (Matacil) is an organic chemical compound with the molecular formula C11H16N2O2. It has a colorless or white crystal-like appearance and is most commonly used as an insecticide.
== History == Aminocarb has been extensively used in eastern Canada since 1976 in order to control the spruce budworm. The fate of this chemical in the ecosystem and detection of aminocarb was studied by the use of two-dimensional thin-layer chromatography. The use of thin-layer chromatography helped isolate and identify the methyl amino, amino and hydroxymethyl analogues from the in vitro metabolism of aminocarb by liver homogenates from humans and rats.
Excerpted from Wikipedia’s “aminocarb” article, available under the CC BY-SA 4.0 licence.