A54059
2-(2-Aminoethoxy)ethanol
98%
Synonym(s):
Diethylene glycolamine
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About This Item
Linear Formula:
NH2CH2CH2OCH2CH2OH
CAS Number:
Molecular Weight:
105.14
Beilstein/REAXYS Number:
906728
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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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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.
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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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-
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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
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