Key Documents

View All Documentation

123056

4-(2-Aminoethyl)aniline

Name: 4-(2-Aminoethyl)aniline
Brand: ALDRICH

97%

Synonym(s):

4-Aminophenethylamine

Select a Size

Change View

About This Item

Linear Formula:

H₂NC₆H₄CH₂CH₂NH₂

CAS Number:

13472-00-9

Molecular Weight:

136.19

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24847518

EC Number:

236-739-2

Beilstein/REAXYS Number:

1099913

MDL number:

MFCD00008194

Assay:

97%

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

200

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

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

Description

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.

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405

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

新产品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Oxidase enzyme immobilisation through electropolymerised films to assemble biosensors for batch and flow injection analysis.

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

High-affinity binding proteins for N-acetylchitooligosaccharide elicitor in the plasma membranes from wheat, barley and carrot cells: conserved presence and correlation with the responsiveness to the elicitor.

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

Studies on the reductive amination of 3-deoxy-D-manno-octulosonic acid (Kdo).

H D Grimmecke et al.

Glycoconjugate journal, 15(6), 555-562 (1999-01-09)

Reductive amination of 3-deoxy-D-manno-octulosonic acid (Kdo) with allylamine (AIIN) or 2-(4-aminophenyl)ethylamine (APEA) yields epimer pairs of 2-N-allylamino and 2-N-[2-(4-aminophenyl)ethylamino]-2,3-dideoxy-D-glycero-D-galacto- and -2,3-dideoxy-D-glycero-D-talo-octonic acid. The yields were 50-60% due to reduction of Kdo to the respective polyols as side reaction products. Mass

View All Related Papers

Global Trade Item Number

SKU	GTIN
123056-10G	04061836825003
123056-1G	04061838721983
123056-5G	04061838721990