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397261

Sigma-Aldrich

N-(2-Aminoethyl)acetamide

technical grade, 90%

Sinónimos:

N-Acetylethylenediamine

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About This Item

Fórmula lineal:
CH3C(O)NHCH2CH2NH2
Número de CAS:
1001-53-2
Peso molecular:
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)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «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)
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
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

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