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  2. 4-Aminophenol - Wikipedia

    en.wikipedia.org/wiki/4-Aminophenol

    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 .

  3. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75

  4. 2,2,4-Trimethyl-1,2-dihydroquinoline - Wikipedia

    en.wikipedia.org/wiki/2,2,4-Trimethyl-1,2-di...

    2,2,4-Trimethyl-1,2-dihydroquinoline (usually abbreviated TMQ, known historically as Acetone-anil) is an aminic antioxidant commonly used as a stabiliser in rubbers and some plastics. Synthesis [ edit ]

  5. Aminophenol - Wikipedia

    en.wikipedia.org/wiki/Aminophenol

    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

  6. Category:Aminophenols - Wikipedia

    en.wikipedia.org/wiki/Category:Aminophenols

    Aminophenol; 2-Aminophenol; 3-Aminophenol; 4-Aminophenol; G. Glycin This page was last edited on 17 March 2021, at 23:44 (UTC). Text is available under the ...

  7. Mesityl oxide - Wikipedia

    en.wikipedia.org/wiki/Mesityl_oxide

    Mesityl oxide is a α,β-unsaturated ketone with the formula CH 3 C(O)CH=C(CH 3) 2. This compound is a colorless, volatile liquid with a honey-like odor. [ 3 ]

  8. C6H7NO - Wikipedia

    en.wikipedia.org/wiki/C6H7NO

    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 ...

  9. Acetanilide - Wikipedia

    en.wikipedia.org/wiki/Acetanilide

    Acetanilide can be produced by reacting acetic anhydride with aniline: [7]. C 6 H 5 NH 2 + (CH 3 CO) 2 O → C 6 H 5 NHCOCH 3 + CH 3 COOH. The preparation used to be a traditional experiment in introductory organic chemistry lab classes, [8] but it has now been widely replaced by the preparation of either paracetamol or aspirin, both of which teach the same practical techniques (especially ...