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  2. 1-Propanol (data page) - Wikipedia

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

    Phase behavior Triple point: 148.75 K (–124.4 °C), ? Pa Critical point: 536.9 K (263.8 °C), 5200 kPa Std enthalpy change of fusion, Δ fus H o: 5.37 kJ/mol

  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

    There are two isomers of propanol. 1-Propanol , n -propanol, or propan-1-ol: CH 3 CH 2 CH 2 OH, the most common meaning 2-Propanol, isopropyl alcohol , isopropanol, or propan-2-ol: (CH 3 ) 2 CHOH

  5. Isopropyl alcohol (data page) - Wikipedia

    en.wikipedia.org/wiki/Isopropyl_alcohol_(data_page)

    4 Vapor pressure of Iso-propyl Alcohol. 5 Distillation data. 6 Spectral data. 7 References. Toggle the table of contents. ... Index of refraction, n D: 1.3776 at 20°C

  6. Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Amyl_alcohol

    Amyl alcohols are alcohols with the formula C 5 H 11 OH. [1] Eight are known. A mixture of amyl alcohols (also called amyl alcohol) can be obtained from fusel alcohol.Amyl alcohol is used as a solvent and in esterification, by which is produced amyl acetate and other products.

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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. The propionaldehyde vapor is immediately condensed into a suitable receiver.

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