Skip to Content
MilliporeSigma
All Photos(1)

Documents

901154

Sigma-Aldrich

2-(2-(2-Ethoxyethoxy)ethoxy)ethanamine

Synonym(s):

3,6,9-Trioxaundecylamine, N-[2-(2-(2-Ethoxyethoxy)ethoxy)ethyl]amine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C8H19NO3
CAS Number:
Molecular Weight:
177.24
MDL number:
UNSPSC Code:
12352116
NACRES:
NA.22

form

liquid

Quality Level

density

0.974

InChI

1S/C8H19NO3/c1-2-10-5-6-12-8-7-11-4-3-9/h2-9H2,1H3

InChI key

WWJVRDMJNJTOBL-UHFFFAOYSA-N

Application

2-(2-(2-Ethoxyethoxy)ethoxy)ethanamine can be used as a reactant to synthesize:
  • 2-(2-(2-(2-Ethoxyethoxy)ethoxy)ethyl)-4-nitroisoindoline-1,3-dione, a key intermediate used to prepare excited-state intramolecular proton transfer (ESIPT)-based fluorescent probe for the detection of palladium.
  • Acetamidine derivatives by condensation reaction with N,N-dimethylacetamide dimethyl acetal.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

230.0 °F

flash_point_c

110 °C


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

A water soluble ESIPT-based fluorescent chemodosimeter for the ratiometric detection of palladium ions in aqueous solution and its application in live-cell imaging
Huang J, et al.
New. J. Chem., 42(19), 15587-15592 (2018)
Jitendra R Harjani et al.
The Journal of organic chemistry, 76(6), 1683-1691 (2011-02-15)
The condensation of primary amine with N,N-dimethylacetamide dimethyl acetal yields a mixture of acetamidine and imidate ester. The product distribution in this reaction depends on the temperature, solvent, and structure of the primary amine. It is possible to suppress the

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