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2. Isopropyl alcohol (data page) - Wikipedia

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

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3. 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 ...

4. Rubbing alcohol - Wikipedia

   en.wikipedia.org/wiki/Rubbing_alcohol

   Isopropyl rubbing alcohols contain from 50% to 99% by volume of isopropyl alcohol, the remainder consisting of water. Boiling points vary with the proportion of isopropyl alcohol from 80 to 83 °C (176 to 181 °F); likewise, freezing points vary from −32 to −50 °C (−26 to −58 °F). [6] Surgical spirit BP boils at 80 °C (176 °F). [7]

5. N,N-Diisopropylaminoethanol - Wikipedia

   en.wikipedia.org/wiki/N,N-Diisopropylaminoethanol

   Inhalation and skin contact are expected to be the primary ways of occupational exposure to this chemical. Based on single exposure animal tests, it is considered to be slightly toxic if swallowed or inhaled, moderately toxic if absorbed through skin as well as being corrosive to eyes and skin. [1]

6. Fatty alcohol - Wikipedia

   en.wikipedia.org/wiki/Fatty_alcohol

   1-Heptanol (enanthic alcohol) 7 carbon atoms: C 7 H 16 O 1-Octanol (capryl alcohol) 8 carbon atoms: C 8 H 18 O Pelargonic alcohol (1-nonanol) 9 carbon atoms: C 9 H 20 O 1-Decanol (decyl alcohol, capric alcohol) 10 carbon atoms: C 10 H 22 O Undecyl alcohol (1-undecanol, undecanol, Hendecanol) 11 carbon atoms: C 11 H 24 O Lauryl alcohol ...

7. Diisopropyl ether - Wikipedia

   en.wikipedia.org/wiki/Diisopropyl_ether

   Whereas at 20 °C, diethyl ether will dissolve 1% by weight water, diisopropyl ether dissolves 0.88%. Diisopropyl ether is used as a specialized solvent to remove or extract polar organic compounds from aqueous solutions, e.g. phenols, ethanol, acetic acid.