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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-195-4
Beilstein/REAXYS Number:
906728
MDL number:
Assay:
98%
Form:
liquid
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
WGK 1
flash_point_f
260.6 °F
flash_point_c
127 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Cao-An Vu et al.
ACS omega, 4(12), 14765-14771 (2019-09-26)
Silicon nanowire field-effect transistors (SiNW-FETs) have been demonstrated as a highly sensitive platform for label-free detection of a variety of biological and chemical entities. However, detecting signal from immunoassays by nano-FETs is severely hindered by the distribution of different charged
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)
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
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)
Atsushi Tamura et al.
Journal of biomaterials science. Polymer edition, 28(10-12), 1124-1139 (2017-03-17)
We developed stimuli-labile polyrotaxanes (PRXs) composed of β-cyclodextrin (β-CD), Pluronic as an axle polymer, and acid-cleavable N-triphenylmethyl groups as bulky stopper molecules, and found that the PRXs are potent therapeutics for Niemann-Pick type C disease, because the PRX can effectively
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A54059-100G | 04061833375877 |
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