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A54059

Sigma-Aldrich

2-(2-Aminoethoxy)ethanol

98%

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Synonym(s):
Diethylene glycolamine
Linear Formula:
NH2CH2CH2OCH2CH2OH
CAS Number:
Molecular Weight:
105.14
Beilstein/REAXYS Number:
906728
EC Number:
MDL number:
PubChem Substance ID:

Quality Level

assay

98%

form

liquid

bp

218-224 °C (lit.)

density

1.048 g/mL at 25 °C (lit.)

SMILES string

NCCOCCO

InChI

1S/C4H11NO2/c5-1-3-7-4-2-6/h6H,1-5H2

InChI key

GIAFURWZWWWBQT-UHFFFAOYSA-N

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1 of 4

This Item
D155624476234128252
2-(2-Aminoethoxy)ethanol 98%

A54059

2-(2-Aminoethoxy)ethanol

2,2-Dimethyl-1,3-dioxolane 98%

D155624

2,2-Dimethyl-1,3-dioxolane

2-Allyloxyethanol 98%

476234

2-Allyloxyethanol

Ethylene sulfide 98%

128252

Ethylene sulfide

density

1.048 g/mL at 25 °C (lit.)

density

0.926 g/mL at 25 °C (lit.)

density

0.955 g/mL at 25 °C (lit.)

density

1.01 g/mL at 25 °C (lit.)

form

liquid

form

liquid

form

-

form

liquid

bp

218-224 °C (lit.)

bp

92-93 °C (lit.)

bp

159 °C (lit.)

bp

55-56 °C (lit.)

Application

2-(2-Aminoethoxy)ethanol is commonly used as a spacer/linker in the synthesis of bioconjugate materials for applications such as drug delivery and protein labeling. It is also employed as a receptor chain in the preparation of carboxamidoquinoline based water-soluble, ratiometric fluorescent zinc sensor.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible, corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

260.6 °F

flash_point_c

127 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Michael J Murcia et al.
Journal of the American Chemical Society, 130(45), 15054-15062 (2008-10-22)
The current study reports the facile design of quantum dot (QD)-conjugated lipids and their application to high-speed tracking experiments on cell surfaces. CdSe/ZnS core/shell QDs with two types of hydrophilic coatings, 2-(2-aminoethoxy)ethanol (AEE) and a 60:40 molar mixture of 1,2-dipalmitoyl-
Yuliya V Sherstyuk et al.
Molecular diversity, 21(1), 101-113 (2016-09-30)
A versatile strategy for the synthesis of [Formula: see text] mimetics was developed, involving an efficient pyrophosphate linkage formation in key conjugates containing a functional amino group which acts as useful reactive anchor for further derivatization. These [Formula: see text]
B Combourieu et al.
Applied and environmental microbiology, 64(1), 153-158 (1998-01-22)
Resting Mycobacterium aurum MO1 cells were incubated with morpholine, a waste from the chemical industry. The kinetics of biodegradation was monitored by using in situ nuclear magnetic resonance (NMR). The incubation medium was directly analyzed by 1H NMR. This technique
Superresolution imaging of targeted proteins in fixed and living cells using photoactivatable organic fluorophores.
Lee, Hsiao-lu D et al.
Journal of the American Chemical Society, 132(43), 15099-15101 (2010)
HaloTag: a novel protein labeling technology for cell imaging and protein analysis.
Los, Georgyi V et al.
ACS Chemical Biology, 3(6), 373-382 (2008)

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