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A solution of nitric acid, water and alcohol, nital, is used for etching metals to reveal the microstructure. ISO 14104 is one of the standards detailing this well known procedure. [45] Nitric acid is used either in combination with hydrochloric acid or alone to clean glass cover slips and glass slides for high-end microscopy applications. [46]
Strong acids/bases (nitric acid, sodium hydroxide), calcium oxide, anhydrous zinc chloride can be corrosive GHS05: Corrosive Explosives, divisions 1.5, 1.6; Flammable gases, category 2; Self-reactive substances and mixtures, type G (see HAZMAT Class 4 Flammable solids) Organic peroxides, type G; no pictogram required
The previous hazard symbols for chemicals, were introduced in the Directive Directive 67/548/EEC, in 1967, and required to be adopted no later than 1 January 1970. [6] The symbols were also included as a part of Directive 1999/45/EC. [7]
"Nitric Acid, Butylester." Butyl Nitrate (928-45-0),Butyl Nitrate (928-45-0) Manufacturers & Suppliers,Synthesis,MSDS. N.p., n.d. Web. 11 Oct. 2012.
Methyl nitrate is a sensitive explosive.When ignited it burns extremely fiercely with a gray-blue flame. Methyl nitrate is a very strong explosive with a detonation velocity of 6,300 m/s, [8] like nitroglycerin, ethylene glycol dinitrate, and other nitrate esters.
The anion [Ce(NO 3) 6] 2− is generated by dissolving Ce 2 O 3 in hot and concentrated nitric acid (HNO 3). [2] The salt consists of the hexanitratocerate(IV) anion [Ce(NO 3) 6] 2− and a pair of ammonium cations NH + 4. The ammonium ions are not involved in the oxidising reactions of this salt.
Hydroxylammonium nitrate or hydroxylamine nitrate (HAN) is an inorganic compound with the chemical formula [NH 3 OH] + [NO 3] −.It is a salt derived from hydroxylamine and nitric acid.
It hydrolyzes in moist air to acetic acid and nitric acid. Alternatively, nitric acid adds to ketene. [2] For aromatic nitrations, acetyl nitrate is generated in situ by mixing nitric acid with an excess of acetic anhydride in the presence of the aromatic substrate. [3] It acetylates amines, akin to the behavior of acetyl chloride:
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