Aniline - Wikipedia Aniline (From Portuguese: anil, meaning ' indigo shrub ', and -ine indicating a derived substance) [6] is an organic compound with the formula C6H5NH2 Consisting of a phenyl group (−C6H5) attached to an amino group (−NH2), aniline is the simplest aromatic amine
Aniline | C6H5NH2 | CID 6115 - PubChem Signs and Symptoms of Acute Aniline Exposure: Signs and symptoms of acute exposure to aniline may be severe and include dyspnea (shortness of breath), respiratory paralysis, cardiac arrhythmias, and cardiovascular collapse
Aniline - Structure, Properties, Preparation, Reactions, Uses It can undergo various reactions to form several other compounds Some of the common reactions of aniline is mentioned below: Coupling Reactions: Aniline reacts with a diazonium salt in a diazo coupling reaction, and form azo dye (like aminoazobenzene) with water and hydrogen chloride as byproducts C6H5N2+Cl- + C6H5NH2 → C6H5N=NC6H4NH2 + H2O
Aniline | Aromatic, Synthesis, Dyeing | Britannica aniline, an organic base used to make dyes, drugs, explosives, plastics, and photographic and rubber chemicals Aniline was first obtained in 1826 by the destructive distillation of indigo
Aniline: Properties, Reactions, Production And Uses Aniline, also known as aminobenzene, is an aromatic amine with the chemical formula C 6 H 5 NH 2 It is a flammable colorless to slightly yellow liquid with a sweet, amine-like odor, and it turns brown upon exposure to air and light
Reactions of Aniline - Chemistry Steps Whether a substituted aniline is more or less basic than aniline depends on the nature of the substituent Electron-donating groups increase the electron density of the benzene ring, making the arylamine more basic than aniline
Aniline | Formula, Properties Application Aniline, also known as phenylamine or aminobenzene, is a simple yet significant organic compound used across a myriad of industrial applications It is an aromatic amine, recognized by its distinctively pungent, fishy smell