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  2. Dihydrolevoglucosenone - Wikipedia

    en.wikipedia.org/wiki/Dihydrolevoglucosenone

    It is miscible with water and many organic solvents. [11] Dihydrolevoglucosenone has a boiling point of 226 °C at 101.325 kPa (vs 202 °C for NMP), and a vapor pressure of 12.98 Pa near room temperature (25 °C). [1] It has a comparatively high dynamic viscosity of 14.5 cP (for comparison DMF: 0.92 cP at 20 °C, NMP: 1.67 cP at 25 °C). [12]

  3. Anhydrous - Wikipedia

    en.wikipedia.org/wiki/Anhydrous

    Many processes in chemistry can be impeded by the presence of water; therefore, it is important that water-free reagents and techniques are used. In practice, however, it is very difficult to achieve perfect dryness; anhydrous compounds gradually absorb water from the atmosphere so they must be stored carefully.

  4. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    In chemistry, a dehydration reaction is a chemical reaction that involves the loss of water from the reacting molecule or ion. Dehydration reactions are common processes, the reverse of a hydration reaction .

  5. HAZMAT Class 5 Oxidizing agents and organic peroxides

    en.wikipedia.org/wiki/HAZMAT_Class_5_Oxidizing...

    5.1: Liquid Any material which exhibits a mean pressure rise time less than or equal to the pressure rise time of a 1:1 nitric acid (65 percent)/cellulose mixture and the criteria for Packing Group I and II are not met. Group II 5.2: All All Division 5.2 materials do not have a packing group in Column 5 of the 49 CFR 172.101 Table.

  6. Tetrachloroethylene - Wikipedia

    en.wikipedia.org/wiki/Tetrachloroethylene

    Tetrachloroethylene is an excellent nonpolar solvent for organic materials. Additionally, it is volatile, highly stable (easily recycled) and nonflammable, and has low toxicity. For these reasons, it has been widely used in dry cleaning worldwide since the 1930s.

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  8. N,N-Diisopropylethylamine - Wikipedia

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

    N,N-Diisopropylethylamine, or Hünig's base, is an organic compound that is a tertiary amine. It is named after the German chemist Siegfried Hünig . It is used in organic chemistry as a non-nucleophilic base. It is commonly abbreviated as DIPEA, DIEA, or i-Pr 2 NEt.

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