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  2. Sodium formate - Wikipedia

    en.wikipedia.org/wiki/Sodium_formate

    In the laboratory, sodium formate can be prepared by neutralizing formic acid with sodium carbonate. It can also be obtained by reacting chloroform with an alcoholic solution of sodium hydroxide . CHCl 3 + 4 NaOH → HCOONa + 3 NaCl + 2 H 2 O

  3. Formic acid - Wikipedia

    en.wikipedia.org/wiki/Formic_acid

    Formic acid (from Latin formica 'ant'), systematically named methanoic acid, is the simplest carboxylic acid, and has the chemical formula HCOOH and structure H−C(=O)−O−H. It is an important intermediate in chemical synthesis and occurs naturally, most notably in some ants.

  4. Formate - Wikipedia

    en.wikipedia.org/wiki/Formate

    Methanol and carbon monoxide react in the presence of a strong base, such as sodium methoxide: [1] CH 3 OH + CO → HCOOCH 3. Hydrolysis of methyl formate gives formic acid and regenerates methanol: HCOOCH 3 → HCOOH + CH 3 OH. Formic acid is used for many applications in industry. Formate esters often are fragrant or have distinctive odors.

  5. Methyl formate - Wikipedia

    en.wikipedia.org/wiki/Methyl_formate

    In the laboratory, methyl formate can be produced by the condensation reaction of methanol and formic acid, as follows: . HCOOH + CH 3 OH → HCOOCH 3 + H 2 O. Industrial methyl formate, however, is usually produced by the combination of methanol and carbon monoxide (carbonylation) in the presence of a strong base, such as sodium methoxide: [4]

  6. Sodium stearate - Wikipedia

    en.wikipedia.org/wiki/Sodium_stearate

    Sodium stearate is produced as a major component of soap upon saponification of oils and fats. The percentage of the sodium stearate depends on the ingredient fats. Tallow is especially high in stearic acid content (as the triglyceride), whereas most fats only contain a few percent. The idealized equation for the formation of sodium stearate ...

  7. Acetic formic anhydride - Wikipedia

    en.wikipedia.org/wiki/Acetic_formic_anhydride

    Acetic formic anhydride is an organic compound with the chemical formula C 3 H 4 O 3, which can be viewed as the mixed anhydride of acetic acid and formic acid. It is used on a laboratory-scale as a formylating agent. [1]

  8. Triethyl orthoformate - Wikipedia

    en.wikipedia.org/wiki/Triethyl_orthoformate

    This colorless volatile liquid, the ortho ester of formic acid, is commercially available. The industrial synthesis is from hydrogen cyanide and ethanol. [1] It may also be prepared from the reaction of sodium ethoxide, formed in-situ from sodium and absolute ethanol, and chloroform: [2] CHCl 3 + 3 Na + 3 EtOH → HC(OEt) 3 + 3 ⁄ 2 H 2 + 3 NaCl

  9. Formyl cyanide - Wikipedia

    en.wikipedia.org/wiki/Formyl_cyanide

    Formyl cyanide is a simple organic compound with the formula HCOCN and structure HC(=O)−C≡N. It is simultaneously a nitrile (R−C≡N) and an aldehyde (R−CH=O). Formyl cyanide is the simplest member of the acyl cyanide family. It is known to occur in space in the Sgr B2 molecular cloud. [1]