Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

397261

Sigma-Aldrich

N-(2-Aminoethyl)acetamide

technical grade, 90%

Synonym(s):

N-Acetylethylenediamine

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
CH3C(O)NHCH2CH2NH2
CAS Number:
1001-53-2
Molecular Weight:
102.14
Beilstein:
1743120
MDL number:
MFCD00008163
UNSPSC Code:
12352100
PubChem Substance ID:
24864696
NACRES:
NA.22

grade

technical grade

Assay

90%

refractive index

n20/D 1.485 (lit.)

bp

128 °C/3 mmHg (lit.)

mp

50 °C (lit.)

density

1.066 g/mL at 25 °C (lit.)

SMILES string

CC(=O)NCCN

InChI

1S/C4H10N2O/c1-4(7)6-3-2-5/h2-3,5H2,1H3,(H,6,7)

InChI key

DAKZISABEDGGSV-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

N-(2-Aminoethyl)acetamide is an organic building block.

Application

N-(2-Aminoethyl)acetamide may be used in the preparation of mixed two-component monolayers on glassy carbon. It may be used in the synthesis of lysidine.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

>230.0 °F - closed cup

Flash Point(C)

> 110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

Acetamide ~99% (GC)

Sigma-Aldrich

A0500

Acetamide

Ethylenediamine ReagentPlus®, ≥99%

Sigma-Aldrich

E26266

Ethylenediamine

The Mechanism of Acid Hydrolysis of Lysidine and N-(2-Aminotheyl) acetamide and Related Amides.
Haake P and Watson J.
The Journal of Organic Chemistry, 35(12), 4063-4067 (1970)
Yoonkyung Kim et al.
Purinergic signalling, 5(1), 39-50 (2008-07-05)
As a continued effort to develop multivalent ligands to enhance the pharmacological effects of monomeric drugs, DITC-APEC, a chemically reactive nucleoside A(2A) adenosine receptor (AR) agonist, was employed to derivatize the surface of third-generation (G3) polyamidoamine (PAMAM) dendrimers. The resulting
Enrique Huang Kwan et al.
Dalton transactions (Cambridge, England : 2003), 45(40), 15931-15941 (2016-07-08)
A new long-tethered boron-containing (P-B-P)-pincer ligand 8 has been synthesized. Complexation of 8 with [Ir(coe)
Emma J Wright et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 20(19), 5550-5554 (2014-04-12)
Mixed two-component monolayers on glassy carbon are prepared by electrochemical oxidation of N-(2-aminoethyl)acetamide and mono-N-Boc-hexamethylenediamine in mixed solution. Subsequent N-deprotection, amide coupling and solid-phase synthetic steps lead to electrode-surface functionalisation with maleimide, with controlled partial coverage of this cysteine-binding group
Ling Li et al.
Molecular cell, 80(3), 525-540 (2020-10-18)
Well-balanced and timed metabolism is essential for making a high-quality egg. However, the metabolic framework that supports oocyte development remains poorly understood. Here, we obtained the temporal metabolome profiles of mouse oocytes during in vivo maturation by isolating large number of

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service