A54059
2-(2-Aminoethoxy)ethanol
98%
Sinônimo(s):
Diethylene glycolamine
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About This Item
Fórmula linear:
NH2CH2CH2OCH2CH2OH
Número CAS:
Peso molecular:
105.14
Beilstein:
906728
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
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Ensaio
98%
Formulário
liquid
p.e.
218-224 °C (lit.)
densidade
1.048 g/mL at 25 °C (lit.)
cadeia de caracteres SMILES
NCCOCCO
InChI
1S/C4H11NO2/c5-1-3-7-4-2-6/h6H,1-5H2
chave InChI
GIAFURWZWWWBQT-UHFFFAOYSA-N
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Aplicação
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.
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Dam. 1 - Skin Corr. 1B
Código de classe de armazenamento
8A - Combustible corrosive hazardous materials
Classe de risco de água (WGK)
WGK 1
Ponto de fulgor (°F)
260.6 °F
Ponto de fulgor (°C)
127 °C
Equipamento de proteção individual
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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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]
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