Aniline

High Chemical Reactivity Aniline’s active amino group renders it a dynamic building block in organic synthesis, readily undergoing salt formation, alkylation, acylation, and diazotization.

Broad Synthetic Utility It acts as a primary precursor for a vast array of fine chemicals, including benzene derivatives, azo compounds, pigments, and synthetic dyes.

Excellent Organic Solvency Exhibiting broad miscibility with common organic solvents—such as ethanol, diethyl ether, and chloroform—it seamlessly integrates into diverse synthetic workflows.

 Core Industrial Intermediate As the foundational aromatic amine, its structural stability combined with broad functional versatility makes it indispensable across modern chemical manufacturing.

Product Description
Chemical Properties
Product Usage

Product Description of Aniline CAS#62-53-3

Aniline is the simplest and most industrially significant aromatic amine. Structurally, it derives from benzene, where one hydrogen atom is substituted by an amino group. At room temperature, aniline occurs as a colorless, oily, flammable liquid with a pungent characteristic odor.

Aniline is sparingly soluble in water, with slightly improved solubility at elevated temperatures up to 370°C. It dissolves readily in common organic solvents including ethanol, ether, and chloroform. Upon prolonged exposure to air and sunlight, the liquid gradually darkens to a brown color due to oxidation. Steam distillation is a conventional purification method for aniline. To mitigate oxidative degradation during distillation, a small amount of zinc powder can be added. For long-term stabilization, purified aniline may be treated with 10–15 ppm sodium borohydride (NaBH₄) to further suppress oxidation. Aqueous solutions of aniline exhibit weak alkaline properties.

Chemically, aniline readily undergoes salt-forming reactions with acids. The hydrogen atoms on its amino group are reactive and can be replaced by alkyl or acyl substituents, yielding secondary and tertiary aniline derivatives as well as acylated aniline products. Electrophilic substitution reactions predominantly produce ortho- and para-substituted isomers. Furthermore, aniline can react with nitrites to form diazonium salts, which serve as critical intermediates for the synthesis of numerous benzene derivatives and azo compounds.

Aniline

Aniline Chemical Properties

Melting point -6 °C (lit.)
Boiling point 184 °C (lit.)
density 1.022 g/mL at 25 °C (lit.)
vapor density 3.22 (185 °C, vs air)
vapor pressure 0.7 mm Hg ( 25 °C)
refractive index n20/D 1.586(lit.)
Fp 76 °C
storage temp. 2-8°C
solubility water: soluble
form Liquid
pka4.63(at 25℃)
color APHA: ≤250
Specific Gravity1.021
OdorSweet, amine-like odor detectable at 0.6 to 10 ppm
Relative polarity0.42
PH8.8 (36g/l, H2O, 20℃)
PH Range8.1
explosive limit1.2-11%(V)
Water Solubility 36 g/L (20 ºC)
Merck 14659
BRN 605631
Henry's Law Constant1.91 at 25 °C (thermodynamic method-GC/UV spectrophotometry, Altschuh et al., 1999)
Exposure limitsTLV-TWA skin 2 ppm (~8 mg/m3) (ACGIH), 5 ppm (~19 mg/m3) (MSHA, OSHA, and NIOSH); IDLH 100 ppm (NIOSH).
Dielectric constant7.8(0℃)
Stability:Stable. Incompatible with oxidizing agents, bases, acids, iron and iron salts, zinc, aluminium. Light sensitive. Combustible.
LogP0.9
CAS DataBase Reference62-53-3(CAS DataBase Reference)
IARC2A (Vol. 27, Sup 7, 127)
NIST Chemistry ReferenceAniline(62-53-3)
EPA Substance Registry SystemAniline (62-53-3)
Hazard Codes T,N,F
Risk Statements 23/24/25-40-41-43-48/23/24/25-50-68-48/20/21/22-39/23/24/25-11
Safety Statements 26-27-36/37/39-45-46-61-63-36/37-16
RIDADR UN 1547 6.1/PG 2
OELTWA: None ppm
WGK Germany 2
RTECS BW6650000
F 46243
Autoignition Temperature615 °C
TSCA Yes
HS Code 2921 41 00
HazardClass 6.1
PackingGroup II
Hazardous Substances Data62-53-3(Hazardous Substances Data)
ToxicityLD50 orally in rats: 0.44 g/kg (Jacobson)
IDLA100 ppm

aniline

Product Usage

For decades, aniline has held a vital position among industrial‑grade chemicals. Its largest‑volume application today lies in polyurethane and rubber manufacturing. Lesser quantities are consumed for producing agrochemicals such as herbicides, fungicides, insecticides and animal repellents, as well as defoliants, dyes, antioxidants, antidegradants and vulcanization accelerators.

Beyond industrial manufacturing, aniline can be found as a component in selected household goods, including stove polish, shoe polish, paints, varnishes and marking inks.

aniline