CAS 929-06-6

Diglycolamine

Description:

Diglycolamine, with the CAS number 929-06-6, is an organic compound that belongs to the class of alkanolamines. It is characterized by the presence of two hydroxyl groups (-OH) and an amine group (-NH2) in its molecular structure, which contributes to its properties as a versatile chemical. Diglycolamine is typically a colorless to pale yellow liquid with a mild odor and is hygroscopic, meaning it can absorb moisture from the air. It has a relatively high boiling point and moderate solubility in water, making it useful in various applications. This compound is primarily utilized in the chemical industry as a solvent, a pH adjuster, and as a building block for the synthesis of other chemicals. Additionally, it serves as a corrosion inhibitor and is employed in gas treatment processes to remove acidic gases such as carbon dioxide and hydrogen sulfide. Due to its amine functionality, diglycolamine can also participate in various chemical reactions, including those involving alkylation and acylation.

Formula: C₄H₁₁NO₂

InChI: InChI=1/C4H11NO2/c1-4(6)7-3-2-5/h4,6H,2-3,5H2,1H3

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
• 5-Hydroxy-3-oxapentylamine
• Aminoethoxyethanol
• DGA
• Diethylene glycol amine
• Diethylene glycol monoamine
• Diglycolamine
• Diglycolamine Agent
• Ethanol, 2-(2-aminoethoxy)-
• Nsc 86108
• O-(2-Hydroxyethyl) ethanolamine
• β-(β-Hydroxyethoxy)ethylamine
• β-Hydroxy-β'-aminodiethyl ether
• 2-(2-Aminoethoxy)ethanol
• AMINODIGLYCOL
• ETHYLENE GLYCOL MONO(2-AMINOETHYL) ETHER
• 2-(2-aminoethoxy)-ethano
• dga[qr]
• ADG
• 2-aminoethoxyethanol[qr]
• beta-Hydroxy-beta'-aminoethyl ether
• DIETHYLENE GLYCOLAMINE
• beta-(beta-Hydroxyethoxy)ethylamine

2-(2-Aminoethoxy)ethanol

CAS: 929-06-6

Formula: C₄H₁₁NO₂

Purity: >98.0%(GC)(T)

Color and Shape: Colorless to Light yellow clear liquid

Molecular weight: 105.14

Ref: 3B-A0301

2-(2-Aminoethoxy)ethanol, 98%

CAS: 929-06-6

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

Formula: C₄H₁₁NO₂

Purity: 98%

Color and Shape: Clear colorless to pale yellow, Liquid

Molecular weight: 105.14

Ref: 02-L18897

2-(2-Aminoethoxy)ethanol

CAS: 929-06-6

Formula: H₂NCH₂CH₂OCH₂CH₂OH

Molecular weight: 105.14

Ref: 7W-GK4985

2-(2-Aminoethoxy) Ethanol

CAS: 929-06-6

Formula: C₄H₁₁NO₂

Molecular weight: 105.14

Ref: 4Z-E-157025

Amino-PEG2-alcohol

Controlled Product

CAS: 929-06-6

Applications 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: C₄H₁₁NO₂

Color and Shape: Neat

Molecular weight: 105.14

Ref: TR-A609095

2-(2-Aminoethoxy)ethanol

CAS: 929-06-6

Formula: C₄H₁₁NO₂

Purity: 98.0%

Color and Shape: Clear

Molecular weight: 105.137

Ref: 10-F336044

2-(2-Aminoethoxy)ethanol

CAS: 929-06-6

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: C₄H₁₁NO₂

Purity: Min. 95%

Molecular weight: 105.14 g/mol

Ref: 3D-FA146120