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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. Multiphasic liquid - Wikipedia

    en.wikipedia.org/wiki/Multiphasic_liquid

    Nonpolar solvent A / solvent B / polymer soluble in solvent B and water / water e.g. heptane, dichloromethane, polyethylene oxide, water; Nonpolar solvent A / solvent B / polymer soluble in solvent B and water / salt / water e.g. 16.3% heptane, 21.7% dichloromethane, 9.5% polyethylene oxide, 51.5% water, 0.1% sodium sulfate

  4. Dichloromethane - Wikipedia

    en.wikipedia.org/wiki/Dichloromethane

    Dichloromethane (DCM, methylene chloride, or methylene bichloride) is an organochlorine compound with the formula C H 2 Cl 2. This colorless, volatile liquid with a chloroform -like, sweet odor is widely used as a solvent .

  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. 2-Aminophenol - Wikipedia

    en.wikipedia.org/wiki/2-Aminophenol

    2-Aminophenol is an organic compound with the formula C 6 H 7 NO. Along with its isomer 4-aminophenol , it is an amphoteric molecule and a reducing agent . It is a useful reagent for the synthesis of dyes and heterocyclic compounds . [ 3 ]

  7. Phenol ether - Wikipedia

    en.wikipedia.org/wiki/Phenol_ether

    Diethyl ether has higher water solubility of 8 g per 100 mL, versus diphenyl ether, with a solubility of 0.002 g per 100 mL. [ 3 ] [ 4 ] The presence of the aromatic ring also draws electrons away from the ethereal oxygen, making the hydrolysis of a phenol ether significantly more difficult than that of an alkyl ether. [ 5 ]

  8. Piperonal - Wikipedia

    en.wikipedia.org/wiki/Piperonal

    Piperonal can be prepared by the oxidative cleavage of isosafrole or by using a multistep sequence from catechol or 1,2-methylenedioxybenzene.Synthesis from the latter chemical is accomplished through a condensation reaction with glyoxylic acid followed by cleaving the resulting α-hydroxy acid with an oxidizing agent.

  9. Metol - Wikipedia

    en.wikipedia.org/wiki/Metol

    Metol (or Elon) is a trade name for the organic compound with the formula [HOC 6 H 4 NH 2 (CH 3)] 2 HSO 4. It is the sulfate salt of N -methylaminophenol. This colourless salt is a popular photographic developer used in monochrome photography .