
CAS 929-06-6: Diglycolamine
Formula:C4H11NO2
InChI:InChI=1S/C4H11NO2/c5-1-3-7-4-2-6/h6H,1-5H2
InChI key:InChIKey=GIAFURWZWWWBQT-UHFFFAOYSA-N
SMILES:O(CCN)CCO
Synonyms:- (2-Hydroxyaethyl)-(2-Aminoaethyl)-Aether
- 1-(2-Aminoethoxy)Ethanol
- 1-Amino-2-(2-hydroxyethoxy)ethane
- 2-(2-Aminoethoxy)ethan-1-ol
- 2-(2-Aminoetoxi)Etanol
- 2-(2-Hydroxyethoxy)Ethanaminium
- 2-(2-Hydroxyethoxy)ethylamine
- 2-(Hydroxyethoxy)ethylamine
- 2-Amino-2'-hydroxydiethyl ether
- 2-Aminoethyl 2-hydroxyethyl ether
- 5-Amino-3-oxapentan-1-ol
- See more synonyms
Sort by
Found 7 products.
Amino-PEG2-alcohol
CAS:Controlled ProductApplications 2-(2-Aminoethoxy)ethanol is a widely used reactant that has been used in the preparation of TD-4306 as long-acting β2-agonist for asthma and COPD therapy. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Mckinnell, R.M., et. al.: Bioorg. Med. Chem. Lett., 24, 2871 (2014)Formula:C4H11NO2Color and Shape:NeatMolecular weight:105.142-(2-Aminoethoxy)ethanol
CAS:2-(2-Aminoethoxy)ethanol (2-AE) is a natural compound that has been synthesized from ethanol and 2-aminoethanol. It has been shown to react with sodium carbonate to form stable complexes that are resistant to hydrolysis by amines. The stability of the complex is attributed to the formation of an intermolecular hydrogen bond between the hydroxyl group on the 2-AE molecule and the carboxylate group on the sodium carbonate molecule. 2-AE reacts with benzalkonium chloride, a quaternary ammonium salt, in water vapor to produce an alcohol and a fatty acid, which is then hydrolyzed by glycol ethers into glycolates. This mechanism is similar to that of other reactions involving quaternary ammonium salts, such as those in fatty acids or glycol ethers.Formula:C4H11NO2Purity:Min. 95%Molecular weight:105.14 g/mol2-(2-Aminoethoxy)ethanol
CAS:Purity:98.0%Color and Shape:Liquid, ClearMolecular weight:105.137001037597662-(2-Aminoethoxy)ethanol, 98%
CAS:2-(2-Aminoethoxy)ethanol is used mainly in stripper solutions for applications in electronics, in gas treating to remove carbon dioxide and hydrogen sulfide, and in coolants/lubricants for metal working applications. Other applications of aminoethoxyethanol (ADG) include, inter alia, crop protection products, surfactants and colorants. It is also used as a selective solvent for recovery of aromatics from refinery streams and in preparation of foam stabilizers, wetting and emulsifying agents. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C4H11NO2Purity:98%Color and Shape:Clear colorless to pale yellow, LiquidMolecular weight:105.142-(2-Aminoethoxy)ethanol
CAS:Formula:C4H11NO2Purity:>98.0%(GC)(T)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:105.142-(2-Aminoethoxy)ethanol, 98%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C4H11NO2Purity:98%Color and Shape:Clear colorless to light yellow, LiquidMolecular weight:105.14