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4-Ethylaniline

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4-Ethylaniline Basic information

Product Name:
4-Ethylaniline
Synonyms:
  • 4-ETHYLANILINE FOR SYNTHESIS 100 ML
  • Aniline, p-ethyl- (8CI)
  • P-AMINOETHYLBENZENE
  • P-ETHYLANILINE
  • 1-Amino-4-ethylbenzene
  • 4-aminoethylbenzene
  • 4-ethyl-anilin
  • 4-ethyl-benzenamin
CAS:
589-16-2
MF:
C8H11N
MW:
121.18
EINECS:
209-637-0
Product Categories:
  • Building Blocks
  • C8 to C9
  • Anilines (Building Blocks for Liquid Crystals)
  • Chemical Synthesis
  • Nitrogen Compounds
  • Organic Building Blocks
  • Building Blocks for Liquid Crystals
  • Functional Materials
  • Amines
  • C8
  • Nitrogen Compounds
Mol File:
589-16-2.mol
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4-Ethylaniline Chemical Properties

Melting point:
-5 °C (lit.)
Boiling point:
216 °C (lit.)
Density 
0.975 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.554(lit.)
Flash point:
185 °F
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
Liquid
pka
pK1:5.00(+1) (25°C)
color 
Clear yellow to red-brown
Water Solubility 
immiscible
BRN 
774319
CAS DataBase Reference
589-16-2(CAS DataBase Reference)
NIST Chemistry Reference
4-Ethylaniline(589-16-2)
EPA Substance Registry System
p-Ethylaniline (589-16-2)
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Safety Information

Hazard Codes 
T
Risk Statements 
23/24/25-33
Safety Statements 
36/37/39-45-36/37-28A
RIDADR 
1602
WGK Germany 
3
RTECS 
BX9900000
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
III
HS Code 
29214980

MSDS

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4-Ethylaniline Usage And Synthesis

Chemical Properties

clear yellow to red-brown liquid

Uses

4-Ethylaniline can be used as intermediates of liquid crystal.

Safety Profile

Poison by ingestion, intravenous, and intraperitoneal routes. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. See also N-ETHYLANILINE.

Purification Methods

Dissolve p-ethylaniline in *benzene, then acetylate it. Recrystallise the acetyl derivative (m 93-94o, Hickinbottom & Waine J Chem Soc 1565 1930) from *C6H6/pet ether or EOH, and hydrolyse it by refluxing 50g with 500mL of H2O and 115mL of conc H2SO4 until the solution becomes clear. The amine sulfate is isolated, suspended in H2O and solid KOH is added to generate the free base, which separates. Dry it (KOH), and distil it from zinc dust in a vacuum [Berliner & Berliner J Am Chem Soc 76 6179 1954]. The picrate has m 171-172o (from 1,2-dichloroethane). [Beilstein 12 H 1090, 12 III 2380, 12 IV 2419.]

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