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A54059

Sigma-Aldrich

2-(2-Aminoethoxy)ethanol

98%

Synonym(s):

Diethylene glycolamine

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About This Item

Linear Formula:
NH2CH2CH2OCH2CH2OH
CAS Number:
929-06-6
Molecular Weight:
105.14
Beilstein:
906728
EC Number:
213-195-4
MDL number:
MFCD00008181
UNSPSC Code:
12352100
PubChem Substance ID:
24890972
NACRES:
NA.22

Quality Level

200

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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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
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

260.6 °F

Flash Point(C)

127 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBL2821
STBJ3490
STBJ2141
STBH0175
STBF1243V

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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)
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-
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
C Tournaire-Arellano et al.
Carbohydrate research, 314(1-2), 47-63 (1999-05-07)
Ureido and thioureido derivatives of 2-acetamido-2-deoxy-beta-D-glucose, 1-amino-1-deoxy-D-glucitol and 2-(2-aminoethoxy)ethanol were prepared as N-acetyl-beta-D-hexosaminidase (NAHase) inhibitors and were evaluated on Trichomonas vaginalis NAHase. Although none showed complete inhibition of the enzyme at 100 microM, 1-amino-1-deoxy-D-glucitol derivatives acted as competitive inhibitors of
Ratiometric and water-soluble fluorescent zinc sensor of carboxamidoquinoline with an alkoxyethylamino chain as receptor.
Zhang, Yu et al.
Organic Letters, 10(3), 473-476 (2008)
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