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397261

Sigma-Aldrich

N-(2-Aminoethyl)acetamide

technical grade, 90%

Synonym(s):

N-Acetylethylenediamine

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About This Item

Linear Formula:
CH3C(O)NHCH2CH2NH2
CAS Number:
1001-53-2
Molecular Weight:
102.14
Beilstein/REAXYS Number:
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

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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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

> 110 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

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’.

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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
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
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)

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