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Quality Level
Assay
97%
refractive index
n20/D 1.591 (lit.)
bp
103 °C/0.3 mmHg (lit.)
mp
28-31 °C (lit.)
density
1.034 g/mL at 25 °C (lit.)
SMILES string
NCCc1ccc(N)cc1
InChI
1S/C8H12N2/c9-6-5-7-1-3-8(10)4-2-7/h1-4H,5-6,9-10H2
InChI key
LNPMZQXEPNWCMG-UHFFFAOYSA-N
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General description
4-(2-Aminoethyl)aniline undergoes coupling with carbohydrates by reductive amination to yield modified carbohydrates.
Application
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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
235.4 °F
Flash Point(C)
113 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Certificates of Analysis (COA)
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Find documentation for the products that you have recently purchased in the Document Library.
Physical chemistry chemical physics : PCCP, 14(25), 9219-9229 (2012-05-31)
The neurotransmitter analogue p-aminophenethylamine (APEA) illustrates many of the pitfalls and challenges associated with spectroscopic and conformational analysis of flexible molecules. The combined experimental-theoretical study presented here resolves a long-standing controversy over its conformational energetic preferences. Jet-cooled resonance enhanced two-photon
Biomaterials, 29(19), 2829-2838 (2008-04-18)
A simple chemical modification method using diazonium coupling chemistry was developed to tailor the structure and hydrophilicity of silk fibroin protein. The extent of modification using several aniline derivatives was characterized using UV-vis and 1H NMR spectroscopies, and the resulting
Macromolecules, 27, 1289-1289 (1994)
Polymer Journal, 23, 1511-1511 (1991)
Chem. Abstr., 116, 106932j-106932j (1992)
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