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Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3 (in which the bond angle between the nitrogen and hydrogen is 170°), wherein one or more hydrogen atoms have been replaced by a substituent such as an ...
Amines are used to remove CO 2 in various areas ranging from natural gas production to the food and beverage industry, and have been since 1930. [10] There are multiple classifications of amines, each of which has different characteristics relevant to CO 2 capture.
In organic chemistry, an aromatic amine is an organic compound consisting of an aromatic ring attached to an amine. It is a broad class of compounds that encompasses anilines , but also many more complex aromatic rings and many amine substituents beyond NH 2 .
The hydroxyl of tyrosine can deprotonate at high pH forming the negatively charged phenolate. Because of this one could place tyrosine into the polar, uncharged amino acid category, but its very low solubility in water matches the characteristics of hydrophobic amino acids well.
A diamine is an amine with exactly two amino groups. Diamines are used as monomers to prepare polyamides, polyimides, and polyureas. The term diamine refers mostly to primary diamines, as those are the most reactive. [1] In terms of quantities produced, 1,6-diaminohexane (a precursor to Nylon 6-6) is most important, followed by ethylenediamine. [2]
2-Aminoalcohols are an important class of organic compounds that are often generated by the reaction of amines with epoxides: C 2 H 4 O + R−NH 2 → RNHC 2 H 4 OH. Simple alkanolamines are used as solvents, synthetic intermediates, and high-boiling bases. [2] Hydrogenation or hydride reduction of amino acids gives the
Glavin’s team also found compounds rich in nitrogen and ammonia in the samples, suggesting that Bennu was part of a larger asteroid that formed about 4.5 billion years ago in the frigid, distant ...
The method allow for the synthesis of secondary amines: [29] [30] R 2 C=NR' + R"Li → R 2 R"CN(Li)R' R 2 R"CN(Li)R' + H 2 O → R 2 R"CNHR' + LiOH. This can be expanded to include enolisable carbons in the Mannich reaction, which is a straightforward and commonly used approach for producing β-amino-carbonyl compounds. [31]