4-Aminobenzonitrile

Description :

4-Aminobenzonitrile is used as an amino substituted benzonitrile with hypotensive activity and as a radioprotective agent. It is also used as a derivatization reagent in the capillary zone electrophoretic analysis of aldoses, ketoses and uronic acid.
Chemical Formula: C7H5N2
Molecular Weight: Approximately 105.12 g/mol
Appearance: Typically a white to light brown crystalline solid.
Amino Group (–NH2) attached to the 4-position (para position) of the ring.
Nitrile Group (–CN) attached to the 1-position of the ring.
Intermediate: Used as an intermediate in the synthesis of various organic compounds. The amino and nitrile groups allow for the formation of derivatives with a range of functional properties.
Drug Development: Employed in the synthesis of pharmaceutical compounds, particularly in creating molecules with potential therapeutic properties. Its structure allows for the development of various bioactive compounds.
Reagent: Utilized in chemical research to study reactions involving amino and nitrile groups, or to synthesize new compounds with these functionalities.
Safety: Handle with care using appropriate personal protective equipment (PPE) such as gloves and safety goggles. Work in a well-ventilated area or fume hood.
Toxicity: Specific toxicity data for 4-aminobenzonitrile is not extensively documented, but as with other nitrile and amine-containing compounds, it should be treated with caution. Avoid inhalation, ingestion, or prolonged contact with skin.
Stability: Generally stable under dry conditions. It should be stored in a cool, dry place, protected from light and moisture.
Formulation: Typically handled as a crystalline solid or in solution, depending on its use
Scientific Studies: 4-Aminobenzonitrile is valuable in research due to its role in organic synthesis and material science. Its functional groups provide opportunities for exploring new chemical reactions and applications in various fields.