Skip to Content
Merck
CN
All Photos(1)

Documents

Safety Information

241067

Sigma-Aldrich

2-Methoxyethylamine

99%

Sign Into View Organizational & Contract Pricing

Synonym(s):
2-Aminoethyl methyl ether
Linear Formula:
CH3OCH2CH2NH2
CAS Number:
Molecular Weight:
75.11
Beilstein:
741854
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

liquid

refractive index

n20/D 1.406 (lit.)

bp

95 °C (lit.)

density

0.864 g/mL at 25 °C (lit.)

SMILES string

COCCN

InChI

1S/C3H9NO/c1-5-3-2-4/h2-4H2,1H3

InChI key

ASUDFOJKTJLAIK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Kinetics of reaction of 2-methoxyethylamine with guanosine 5′-phospho-2-methylimidazolide (2-MeImpG) was studied.

Application

2-Methoxyethylamine can be used as a reactant:
  • In the substitution reaction with phosphoimidazolide-activated derivatives of nucleosides.
  • To synthesize amides by reacting with carboxylic acids.
  • For the chemical modification of α-acrylated cross-linked polymer via aza-Michael addition.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

WGK

WGK 3

Flash Point(F)

53.6 °F

Flash Point(C)

12 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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

Mesoporous Structured Silica-An improved catalyst for direct amide synthesis and its application to continuous flow processing.
Comerford J, et al.
ARKIVOC (Gainesville, FL, United States) (2012)
Nathan J Van Zee et al.
Nature, 558(7708), 100-103 (2018-06-01)
Water directs the self-assembly of both natural1,2 and synthetic3-9 molecules to form precise yet dynamic structures. Nevertheless, our molecular understanding of the role of water in such systems is incomplete, which represents a fundamental constraint in the development of supramolecular
A Kanavarioti et al.
The Journal of organic chemistry, 60(3), 632-637 (1995-02-10)
Aliphatic amines react with phosphoimidazolide-activated derivatives of guanosine and cytidine (ImpN) by replacing the imidazole group. The kinetics of reaction of guanosine 5'-phospho-2-methylimidazolide (2-MeImpG) with glycine ethyl ester, glycinamide, 2-methoxyethylamine, n-butylamine, morpholine, dimethylamine (Me2NH), ethylmethylamine (EtNHMe), diethylamine (Et2NH), pyrrolidine, and
Intrinsic green fluorescent cross-linked poly (ester amide) s by spontaneous zwitterionic copolymerization
Zia A, et al.
Biomacromolecules, 22, 4794-4804 (2021)
Courtney H Fox et al.
Nature communications, 6, 7417-7417 (2015-07-16)
Dynamic covalent materials are stable materials that possess reversible behaviour triggered by stimuli such as light, redox conditions or temperature; whereas supramolecular crosslinks depend on the equilibrium constant and relative concentrations of crosslinks as a function of temperature. The combination

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