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2. 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 ...

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. Isopropyl alcohol (data page) - Wikipedia

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

   Phase behavior Triple point: 184.9 K (−88.2 °C), ? Pa Critical point: 508.7 K (235.6 °C), 5370 kPa Std enthalpy change of fusion, Δ fus H o: 5.28 kJ/mol Std entropy change

5. List of cooling baths - Wikipedia

   en.wikipedia.org/wiki/List_of_cooling_baths

   Liquid N 2: Toluene-95 Liquid N 2: Methanol-98 Liquid N 2: Cyclohexene-104 Liquid N 2: Isooctane-107 Liquid N 2: Ethyl iodide-109 Liquid N 2: Carbon disulfide-110 Liquid N 2: Butyl bromide-112 Liquid N 2: Ethanol-116 Liquid N 2: Ethyl bromide-119 Liquid N 2: Acetaldehyde-124 Liquid N 2: Methylcyclohexane-126 Liquid N 2: n-Propanol-127 Liquid N ...

6. 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

7. Alcohol (chemistry) - Wikipedia

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

   When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde , ketone , or carboxylic acid ), then the prefix hydroxy- is used, [ 19 ] e.g., as in 1-hydroxy-2 ...