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Methemoglobinemia is the primary toxic effect of ethyl nitrite. [5] Due to ethyl nitrite's high volatility and faint smell, in the presence of ethyl nitrite vapors, it is easy to breath a high dose of it without realizing, resulting in methemoglobinemia, [ 6 ] which may or may not be severe, or even fatal .
The structure of a nitrile: the functional group is highlighted blue. In organic chemistry, a nitrile is any organic compound that has a −C≡N functional group.The name of the compound is composed of a base, which includes the carbon of the −C≡N, suffixed with "nitrile", so for example CH 3 CH 2 C≡N is called "propionitrile" (or propanenitrile). [1]
Propionitrile, also known as ethyl cyanide and propanenitrile, is an organic compound with the formula CH 3 CH 2 CN. It is a simple aliphatic nitrile. The compound is a colourless, water-soluble liquid. It is used as a solvent and a precursor to other organic compounds. [7]
Acetonitrile is used mainly as a solvent in the purification of butadiene in refineries. Specifically, acetonitrile is fed into the top of a distillation column filled with hydrocarbons including butadiene, and as the acetonitrile falls down through the column, it absorbs the butadiene which is then sent from the bottom of the tower to a second separating tower.
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 ...
The C-N distance in isocyanides is 115.8 pm in methyl isocyanide.The C-N-C angles are near 180°. [3]Akin to carbon monoxide, isocyanides are described by two resonance structures, one with a triple bond between the nitrogen and the carbon and one with a double bond between.
Nitrate esters are typically prepared by condensation of nitric acid and the alcohol: [1] [2] For example, the simplest nitrate ester, methyl nitrate, is formed by reaction of methanol and nitric acid in the presence of sulfuric acid: [3]
Methyl nitrite is a toxic asphyxiating gas, a potent cyanotic agent. Exposure may result in methemoglobinemia. [6]Methyl nitrite is an oxidizing agent and a heat-sensitive explosive; its sensitivity increases in presence of metal oxides.