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2-(4-Aminophenyl)ethylamine

Basic information Safety Supplier Related

2-(4-Aminophenyl)ethylamine Basic information

Product Name:
2-(4-Aminophenyl)ethylamine
Synonyms:
  • 4-(2-AMINOETHYL)ANILINE PURUM 97%
  • p-(2-Aminoethyl)aniline
  • 2-(4-Aminophenyl)ethylamine,95%
  • 1-Amino-2-(4-aminophenyl)ethane 4-(2-Aminoethyl)aniline 4-Aminophenethylamine
  • 4-(2-Aminoethyl)anil
  • 4-Aminophenethylamine, 2-(4-Aminophenyl)ethylamine
  • 4-(2-AMinoethyl)aniline 97%
  • Aminophenethylamine
CAS:
13472-00-9
MF:
C8H12N2
MW:
136.19
EINECS:
236-739-2
Product Categories:
  • Anilines, Aromatic Amines and Nitro Compounds
  • 1
Mol File:
13472-00-9.mol
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2-(4-Aminophenyl)ethylamine Chemical Properties

Melting point:
28-31 °C(lit.)
Boiling point:
103 °C0.3 mm Hg(lit.)
Density 
1.034 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.591(lit.)
Flash point:
>230 °F
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Viscous Liquid
pka
10.32±0.10(Predicted)
color 
Clear light yellow to brown-yellow
Water Solubility 
Insoluble in water.
Sensitive 
Air Sensitive
BRN 
1099913
Stability:
Air Sensitive
CAS DataBase Reference
13472-00-9(CAS DataBase Reference)
NIST Chemistry Reference
2-(4-Aminophenyl)ethylamine(13472-00-9)
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Safety Information

Hazard Codes 
C,Xi
Risk Statements 
34-20/21/22
Safety Statements 
26-36/37/39-45-27
RIDADR 
UN 3259 8/PG 2
WGK Germany 
3
2-10
HazardClass 
8
PackingGroup 
III
HS Code 
29215900

MSDS

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2-(4-Aminophenyl)ethylamine Usage And Synthesis

Chemical Properties

clear light yellow to brown-yellow viscous liquid

Uses

4-(2-Aminoethyl)aniline has been used in chemical modification of silk fibroin to tailor the overall hydrophilicity and structure of silk. It has been used as reagent in polycondensation reactions.

Application

2-(4-Aminophenyl)ethylamine (APEA) is an important amine compound for the study of reductive amination with 3-deoxy-d-mannuronic acid (Kdo) and for the synthesis of new heat-resistant biopolyureas by fermentation techniques[1-2].

Synthesis Reference(s)

Tetrahedron Letters, 25, p. 5219, 1984 DOI: 10.1016/S0040-4039(01)81568-9

General Description

4-(2-Aminoethyl)aniline undergoes coupling with carbohydrates by reductive amination to yield modified carbohydrates.

References

[1] H D GRIMMECKE; H B. Studies on the reductive amination of 3-deoxy-D-manno-octulosonic acid (Kdo).[J]. Glycoconjugate Journal, 1998. DOI:10.1023/a:1006955508077.
[2] HAJIME MINAKAWA. Fermentative production of 2-(4-aminophenyl)ethylamine to synthesize a novel heat-resistant biopolyurea.[J]. Bioscience, Biotechnology, and Biochemistry, 2022. DOI:10.1093/bbb/zbac077.

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