AnodyneWiki

Aniline

Aniline
Aniline
Salts
[]
Aniline hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Aniline hemihemisulfate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
[]
93.13 g/mol [1]
Density1.022 at 68 °F (EPA, 1998) - Denser than water; will sink g/cm3 [1]
AppearanceOily liquid; colorless when freshly distilled, darkens on exposure to air and light [1]
OdorHedonic tone; pungent [1]
TasteBurning taste [1]
Melting point21 ° [1]
Boiling point363 to 367 °F at 760 mmHg (EPA, 1998) [1]
DecompositionHazardous decomposition products formed under fire conditions - Carbon oxides, nitrogen oxides (NOx). [1]
Solubility10 to 50 mg/mL at 73 °F (NTP, 1992) [1]
0.9 [1]
Structural Identifiers
[]
C6H7[1]
aniline [1]
C1=CC=C(C=C1)N [1]
InChI=1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2 [1]
InChIKeyPAYRUJLWNCNPSJ-UHFFFAOYSA-N [1]

Aniline (also known as Aniline, Benzenamine, 62-53-3, Phenylamine, Aminobenzene, Aminophen, Arylamine, Kyanol, Cyanol or Anilin) is a substance of the aniline class.

Chemistry

Salts []

Aniline is typically found in the form of its hydrochloride and hemihemisulfate salts.

 []

Aniline is a achiral mixture.

Pharmacology

Metabolism

Subjective effects []

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 6115, Aniline. Accessed March 5, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/6115

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Aniline. UNII: SIR7XX2F1K. Global Substance Registration System. Accessed March 5, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/SIR7XX2F1K