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Ammonolysis can be used to synthesize nitrides (and oxynitrides) by reacting various metal precursors with ammonia, some options include chemical vapor deposition, [3] treating metals or metal oxides with ammonia gas, [15] or liquid supercritical ammonia (also known as "ammonothermal" synthesis, analogous to hydrothermal synthesis).
1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC, EDAC or EDCI) is a water-soluble carbodiimide usually handled as the hydrochloride. [1] It is typically employed in the 4.0-6.0 pH range. It is generally used as a carboxyl activating agent for the coupling of primary amines to yield amide bonds.
In chemistry, aminolysis (/am·i·nol·y·sis/) is any chemical reaction in which a molecule is lysed (split into two parts) by reacting with ammonia (NH 3) or an amine. [1] The case where the reaction involves ammonia may be more specifically referred to as ammonolysis .
Ethylene chemical structure. Ethylene signaling pathway is a signal transduction in plant cells to regulate important growth and developmental processes. [1] [2] Acting as a plant hormone, the gas ethylene is responsible for promoting the germination of seeds, ripening of fruits, the opening of flowers, the abscission (or shedding) of leaves and stress responses. [3]
An example of a solvolysis reaction is the reaction of a triglyceride with a simple alcohol such as methanol or ethanol to give the methyl or ethyl esters of the fatty acid, as well as glycerol. This reaction is more commonly known as a transesterification reaction due to the exchange of the alcohol fragments.
α-Alkyltryptamines are a group of substituted tryptamines which possess an alkyl group, such as a methyl or ethyl group, attached at the alpha carbon, and in most cases no substitution on the amine nitrogen.
These effects may be exerted as antibacterial, plant growth regulatory or neuromodulatory. They can act as ligands, and heavy metal complexes with aminophosphonates have medical applications. [2] Phosphonates are more difficult to hydrolyse than phosphates. [3] Some aminophosphonates degrade to aminomethylphosphonic acid. [4]
In organic chemistry, an ethyl group (abbr. Et) is an alkyl substituent with the formula −CH 2 CH 3, derived from ethane (C 2 H 6). Ethyl is used in the International Union of Pure and Applied Chemistry 's nomenclature of organic chemistry for a saturated two-carbon moiety in a molecule, while the prefix " eth- " is used to indicate the ...