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  2. File:Propan-1-ol.svg - Wikipedia

    en.wikipedia.org/wiki/File:Propan-1-ol.svg

    Date/Time Thumbnail Dimensions User Comment; current: 21:07, 2 June 2014: 244 × 64 (7 KB): Arrowsmaster: scaled up and changed the OH alignment: 16:18, 5 January 2011

  3. 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.

  4. Propanol - Wikipedia

    en.wikipedia.org/wiki/Propanol

    Propanal (propionaldehyde) differs in spelling from propanol by a single letter and is a different compound. Propranolol is a drug used for reducing blood pressure and hand tremors. Index of chemical compounds with the same name

  5. File:Reaction of Propan-1-ol and Copper(II) oxide to ...

    en.wikipedia.org/wiki/File:Reaction_of_Propan-1...

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  6. Propyl acetate - Wikipedia

    en.wikipedia.org/wiki/Propyl_acetate

    This colorless liquid is known by its characteristic odor of pears. Due to this fact, it is commonly used in fragrances and as a flavor additive. It is formed by the esterification of acetic acid and propan-1-ol, often via Fischer–Speier esterification, with sulfuric acid as a catalyst and water produced as a byproduct. [6]

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  8. Propionaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propionaldehyde

    Propionaldehyde may also be prepared by oxidizing 1-propanol with a mixture of sulfuric acid and potassium dichromate.The reflux condenser contains water heated at 60 °C, which condenses unreacted propanol, but allows propionaldehyde to pass.

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