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| 2-(4-Aminophenyl)ethylamine Basic information |
| 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.) | Fp | >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) |
| 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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| 2-(4-Aminophenyl)ethylamine Preparation Products And Raw materials |
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