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4-Aminophenol (or para-aminophenol or p-aminophenol) is an organic compound with the formula H 2 NC 6 H 4 OH. Typically available as a white powder, [ 3 ] it is commonly used as a developer for black-and-white film , marketed under the name Rodinal .
The Solvay process or ammonia–soda process is the major industrial process for the production of sodium carbonate (soda ash, Na 2 CO 3). The ammonia–soda process was developed into its modern form by the Belgian chemist Ernest Solvay during the 1860s. [ 1 ]
At the time it improved streets and the neighborhood, as it extracted underground salts from beneath the Detroit River. By 1969, Solvay was gone. [4] In 1915, during World War I, Split Rock became the site of a munitions factory operated by the Semet-Solvay Company. The plant employed about 2500 people when it exploded on July 2, 1918, killing ...
The three aminophenol isomers: Left: 2-Aminophenol (o-aminophenol) Center: 3-Aminophenol (m-aminophenol) Right: 4-Aminophenol (p-aminophenol) Aminophenol may refer to any of three isomeric chemical compounds: 2-Aminophenol; 3-Aminophenol; 4-Aminophenol; They are simultaneously an aniline and a phenol
Baking powder is made up of a base, an acid, and a buffering material to prevent the acid and base from reacting before their intended use. [5] [6] Most commercially available baking powders are made up of sodium bicarbonate (NaHCO 3, also known as baking soda or bicarbonate of soda) and one or more acid salts.
RODINAL. Rodinal is the trade name of a black and white developing agent produced originally by the German company Agfa based on the chemical 4-aminophenol. [1] Rodinal is a popular high acutance black and white developer and is used at different dilutions for development in rotary machines, by agitation, as well as for stand development.
3-Aminophenol is an organic compound with formula C 6 H 4 (NH 2)(OH). It is an aromatic amine and a phenol . It is the meta isomer of 2-aminophenol and 4-aminophenol .
Benzene can be easily converted to chlorobenzene by nucleophilic aromatic substitution via a benzyne intermediate. [1] It is treated with aqueous sodium hydroxide at 350 °C and 300 bar or molten sodium hydroxide at 350 °C to convert it to sodium phenoxide, which yields phenol upon acidification. [2]