123056
4-(2-Aminoethyl)aniline
97%
Synonym(s):
4-Aminophenethylamine
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About This Item
Linear Formula:
H2NC6H4CH2CH2NH2
CAS Number:
Molecular Weight:
136.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
236-739-2
Beilstein/REAXYS Number:
1099913
MDL number:
Assay:
97%
InChI key
LNPMZQXEPNWCMG-UHFFFAOYSA-N
InChI
1S/C8H12N2/c9-6-5-7-1-3-8(10)4-2-7/h1-4H,5-6,9-10H2
SMILES string
NCCc1ccc(N)cc1
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.)
functional group
amine
Quality Level
Related Categories
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.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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M Reyes-Parada et al.
Biochemical pharmacology, 47(8), 1365-1371 (1994-04-20)
The in vitro and ex vivo monoamine oxidase (MAO) inhibitory effects of (+/-)4-dimethylamino-alpha-methyl-phenethylamine (4-DMAA) and (+/-)4-methylamino-alpha-methyl-phenethylamine (4-MAA) were reassessed, in comparison with the previously unstudied achiral parent compound, 4-dimethyl-aminophenethylamine (4-DMAPEA) and with a salt of 4-DMAA enriched in the levo
Mihaela Badea et al.
Biosensors & bioelectronics, 18(5-6), 689-698 (2003-04-23)
Glucose oxidase, lactate oxidase, L-aminoacid oxidase and alcohol oxidase were immobilised on new films based on 2,6-dihydroxynaphthalene (2,6-DHN) copolymerised with 2-(4-aminophenyl)-ethylamine (AP-EA) onto the Pt electrodes. The electropolymerisation was performed by cyclic voltammetry. Different scan rates and scan potential ranges
Chem. Abstr., 116, 106932j-106932j (1992)
Mitsuo Okada et al.
Plant & cell physiology, 43(5), 505-512 (2002-06-01)
Binding experiments as well as affinity labeling with an (125)I-labeled 2-(4-aminophenyl)ethylamino derivative of N-acetylchitooctaose revealed the presence of high-affinity binding sites/proteins for N-acetylchitooligosaccharide elicitor in the plasma membrane preparation from suspension-cultured carrot cells, barley cells and wheat leaves. Their binding
Polymer Journal, 23, 1511-1511 (1991)
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