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Ethyl nitrate is the ethyl ester of nitric acid and has the chemical formula C 2 H 5 N O 3.It is a colourless, volatile, explosive, and extremely flammable liquid. It is used in organic synthesis with use as a nitrating agent and as an intermediate in the preparation of some drugs, dyes, and perfumes. [1]
Nitrate esters, such as nitroglycerin, are known for their explosive properties, while polyesters are important plastics, with monomers linked by ester moieties. Esters of carboxylic acids usually have a sweet smell and are considered high-quality solvents for a broad array of plastics, plasticizers , resins , and lacquers . [ 2 ]
Ethyl nitrate This page was last edited on 26 August 2022, at 19:57 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
In the United Kingdom, the environmental regulator permits only chemical additives which are classed as non hazardous to groundwater for fracturing fluids. [3] [4] [5] Operators are required to disclose the content of hydraulic fracturing fluids to the relevant environment agency [6] while the composition must be disclosed if the regulator demands it. [7]
One of the main cetane improver additives manufactured today is 2-ethylhexyl nitrate (CAS n°: 27247-96-7) [1] which starts to decompose at 130 °C. 2-ethylhexyl nitrate is the result of the reaction of 2-ethylhexanol and nitric acid.
Likewise pyrrolidine is a substrate for ethyl nitrite. [ 6 ] Alkyl nitrites are also used in the formation of oximes with the stronger carbon acids and acid or base catalysis for example in the reaction of 2-butanone , ethyl nitrite and hydrochloric acid forming the oxime, [ 7 ] the similar reaction with phenacyl chloride , [ 8 ] or the ...
22395-91-1 AlCl 2<F: aluminium chloride fluoride: 22395-91-1 AlClO: aluminium chloride oxide: 13596-11-7 AlCl 2 H: dichloroalumane: 16603-84-2 AlCl 3: aluminium chloride: 16603-84-2 AlCl 2 F: aluminium chloride fluoride: 13497-96-6 AlCl 3: aluminium trichloride: 7446-70-0 AlCl 4 Cs: aluminium caesium tetrachloride: 17992-03-9 AlCl 4 K ...