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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. 1-Propanol (data page) - Wikipedia

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

    Table data obtained from CRC Handbook of Chemistry and Physics 44th ed. log 10 of n-propanol vapor pressure. Uses formula: ... for n-propanol/Cyclohexane [4] P = 101. ...

  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;

  5. Isopropyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Isopropyl_alcohol

    Isopropyl alcohol (IUPAC name propan-2-ol and also called isopropanol or 2-propanol) is a colorless, flammable, organic compound with a pungent alcoholic odor. [9]Isopropyl alcohol, an organic polar molecule, is miscible in water, ethanol, and chloroform, demonstrating its ability to dissolve a wide range of substances including ethyl cellulose, polyvinyl butyral, oils, alkaloids, and natural ...

  6. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    1-propanol, 1-butanol, and isobutyl alcohol for use as a solvent and precursor to solvents; C6–C11 alcohols used for plasticizers, e.g. in polyvinylchloride; fatty alcohol (C12–C18), precursors to detergents; Methanol is the most common industrial alcohol, with about 12 million tons/y produced in 1980.

  7. List of alkanols - Wikipedia

    en.wikipedia.org/wiki/List_of_alkanols

    1-Propanol; Isopropyl alcohol; C4. n-Butanol; Isobutanol; sec-Butanol ... 3,3-Dimethyl-1-butanol This page was last edited on 27 March 2024, at 19:55 ...

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  9. Ehrlich's reagent - Wikipedia

    en.wikipedia.org/wiki/Ehrlich's_reagent

    The reagent is prepared by dissolving 0.5 [5] –2.0 g of p–dimethylaminobenzaldehyde (DMAB) in 50 mL of 95% ethanol and 50 mL of concentrated hydrochloric acid [6] [7] and is best used when fresh. Other alcohols, such as 1-propanol, can also be used as well. [8] The Ehrlich reagent is similar to a number of other indole tests: