4-Ethylaniline
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
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)
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
- Language:English Provider:4-Ethylaniline
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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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