Anodyne

Aniline
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
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Hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Hemisulfate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
[]
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Physical properties
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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
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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]
Toxicity
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Human - child:
- oral: 3125 mg/kg
Dog:
- skin: 1540 mg/kg
- intravenous: 200 mg/kg
Cat:
- oral: 100 mg/kg
- subcutaneous: 100 mg/kg
Rabbit:
- oral: 500 mg/kg
- subcutaneous: 1 gm/kg
Rat:
- oral: 250 mg/kg
- skin: 1400 mg/kg
- intraperitoneal: 420 mg/kg
Mouse:
- oral: 464 mg/kg
- intraperitoneal: 492 mg/kg
- subcutaneous: 200 mg/kg
Dog:
- oral: 195 mg/kg
Cat:
- skin: 254 mg/kg
Rabbit:
- skin: 820 uL/kg
- intravenous: 64 mg/kg
Guinea pig:
- oral: 400 mg/kg
- skin: 1290 mg/kg
- intraperitoneal: 100 mg/kg
Quail:
- oral: 750 mg/kg
Mammal (species unspecified):
- oral: 500 mg/kg
Bird - wild:
- oral: 562 mg/kg

Aniline

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

Chemistry

Salts []

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

 []

Aniline is a achiral mixture

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 6115, Aniline. Accessed August 6, 2025. 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 August 6, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/SIR7XX2F1K