Alkanolamines
Alkanolamines are a class of amine compounds widely used in various industrial applications, particularly in the chemical, petroleum refining, and gas processing sectors. These chemicals are derivatives of primary alcohols, featuring an alkyl chain attached to the nitrogen atom of an amine group (-NH2). The primary function of alkanolamines is their ability to react with acidic gases such as carbon dioxide (CO?) and hydrogen sulfide (H?S), making them highly effective in gas treating processes. They are available in different molecular weights, allowing for tailored applications based on specific operational needs.
Alkanolamines can exist in various forms including liquid solutions or aqueous mixtures. Their basicity and solubility properties enable efficient absorption of acidic gases from natural gas, refinery off-gases, and industrial exhaust streams. Common uses include sour gas treating, amine washing, desulfurization processes, and carbon dioxide removal for enhanced oil recovery (EOR) applications.
The selection of an appropriate alkanolamine often depends on factors such as temperature, pressure conditions, and the specific impurities to be removed from the process stream. Due to their effectiveness in purifying gases, alkanolamines play a crucial role in environmental protection and industrial efficiency.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Heptadecanamide, N-(2-hydroxyethyl)- | 53832-59-0 | C19H39NO2 |
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Ethanol,2-[bis(hydroxymethyl)amino]- | 73391-91-0 | C4H11NO3 |
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Ethanol, 2-[(2-hydrazinoethyl)amino]- | 88303-65-5 | C4H13N3O |
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2-{2-(dimethylamino)ethylamino}ethan-1-ol | 38361-86-3 | C6H16N2O |
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Ethanol, 2-amino-, polymer with methyloxirane and oxirane | 32439-74-0 | C7H17NO3 |
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5-aminopent-1-en-3-ol | 87487-96-5 | C5H11NO |
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1,4,10,13-Tetraoxa-7,16-diazacyclooctadecane,7,16-bis(methoxymethyl)- | 83809-94-3 | C16H34N2O6 |
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L-Methioninol | 2899-37-8 | C5H13NOS |
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L-Threoninol | 3228-51-1 | C4H11NO2 |
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6-Amino-1-hexanol | 4048-33-3 | C6H15NO |
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