A54059
2-(2-Aminoethoxy)ethanol
98%
Synonym(s):
Diethylene glycolamine
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100 G
€48.50
About This Item
Linear Formula:
NH2CH2CH2OCH2CH2OH
CAS Number:
Molecular Weight:
105.14
Beilstein:
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.[1][2][3] It is also employed as a receptor chain in the preparation of carboxamidoquinoline based water-soluble, ratiometric fluorescent zinc sensor.[4]
Signal Word
Danger
Hazard Statements
Precautionary Statements
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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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
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)
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
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