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  2. 1-Propanol - Wikipedia

    en.wikipedia.org/wiki/1-Propanol

    1-Propanol (also propan-1-ol, propanol, n-propyl alcohol) is a primary alcohol with the formula CH 3 CH 2 CH 2 OH and sometimes represented as PrOH or n-PrOH.It is a colourless liquid and an isomer of 2-propanol. 1-Propanol is used as a solvent in the pharmaceutical industry, mainly for resins and cellulose esters, and, sometimes, as a disinfecting agent.

  3. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  4. Propyl propanoate - Wikipedia

    en.wikipedia.org/wiki/Propyl_propanoate

    It is the ester of propanol and propionic acid. Like most esters, propyl propanoate is a colorless liquid with a fruity odor. The scent of propyl propionate is described as a chemically tinged pineapple or pear. It is used in perfumery and as a solvent. [2] [3] The refractive index at 20 °C is 1.393.

  5. 1-Propanol (data page) - Wikipedia

    en.wikipedia.org/wiki/1-Propanol_(data_page)

    This page provides supplementary chemical data on 1-Propanol (n-propanol). Material Safety Data Sheet The handling of this chemical may incur notable safety ...

  6. Propanamide - Wikipedia

    en.wikipedia.org/wiki/Propanamide

    Propanamide has the chemical formula CH 3 CH 2 C=O(NH 2). [1] It is the amide of propanoic acid. This organic compound is a mono-substituted amide. [2] Organic compounds of the amide group can react in many different organic processes to form other useful compounds for synthesis.

  7. Methyl propionate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propionate

    Methyl propionate can be prepared by esterification of propionic acid with methanol. Industrially, it is prepared by carboalkoxylation, i.e., the reaction of ethylene with carbon monoxide and methanol in the presence of a catalyst: C 2 H 4 + CO + MeOH → MeO 2 CCH 2 CH 3. The reaction is catalyzed by nickel carbonyl and palladium(0) complexes ...

  8. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  9. Ammonium propionate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_propionate

    propanoic acid, ammonium salt(1:1) Identifiers ... It is formed by the reaction of propionic acid and ammonia. Uses. It is used in several products, which include ...