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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 .
Solubility tables; Substance Formula 0 °C 10 °C 15 °C 20 °C 30 °C 40 °C 50 °C ... Fe 2 (SO 4) 3 ·H 2 O: 25.6: L. Substance Formula 0 °C 10 °C
Acetone and acetic anhydride ((CH 3 C(O)) 2 O) upon the addition of boron trifluoride (BF 3) catalyst: [11] (CH 3 C(O)) 2 O + CH 3 C(O)CH 3 → CH 3 C(O)CH 2 C(O)CH 3. A second synthesis involves the base-catalyzed condensation (e.g., by sodium ethoxide CH 3 CH 2 O − Na +) of acetone and ethyl acetate, followed by acidification of the sodium ...
The molecular formula C 6 H 7 NO (molar mass: 109.13 g/mol) may refer to: Aminophenols. 2-Aminophenol; 3-Aminophenol; 4-Aminophenol; Nicotinyl alcohol ...
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
Diacetone alcohol, mesityl oxide, and 3-hydroxy-3,5,5-trimethylcyclohexan-1-one are intermediates. A side product is beta-isophorone , where the C=C group is not conjugated with the ketone. [ 4 ]
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 .
2 K 4 [Fe(CN) 6] + Cl 2 → 2 K 3 [Fe(CN) 6] + 2 KCl. This reaction can be used to remove potassium hexacyanidoferrate(II) from a solution. [citation needed] A famous reaction involves treatment with ferric salts, most commonly Iron(III) chloride, to give Prussian blue. In the reaction with Iron(III) chloride, producing Potassium chloride as a ...