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  2. Pentaerythritol tetranitrate - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol_tetranitrate

    Pentaerythritol tetranitrate (PETN), also known as PENT, pentyl, PENTA (ПЕНТА, primarily in Russian), TEN (tetraeritrit nitrate), corpent, or penthrite (or, rarely and primarily in German, as nitropenta), is an explosive material. It is the nitrate ester of pentaerythritol, and is structurally very similar to nitroglycerin.

  3. Xylitol pentanitrate - Wikipedia

    en.wikipedia.org/wiki/Xylitol_pentanitrate

    Xylitol pentanitrate (XPN) is a nitrated ester primary explosive [3] [4] first synthesized in 1891 by Gabriel Bertrand. [5] [6] Law enforcement has taken an interest in XPN along with erythritol tetranitrate (ETN) and pentaerythritol tetranitrate (PETN) due to their ease of synthesis, which makes them accessible to amateur chemists and terrorists.

  4. Pentyl nitrite - Wikipedia

    en.wikipedia.org/wiki/Pentyl_nitrite

    This pharmacology -related article is a stub. You can help Wikipedia by expanding it.

  5. Ethyl nitrate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_nitrate

    Ethyl nitrate is the ethyl ester of nitric acid and has the chemical formula C 2 H 5 N O 3.It is a colourless, volatile, explosive, and extremely flammable liquid. It is used in organic synthesis with use as a nitrating agent and as an intermediate in the preparation of some drugs, dyes, and perfumes. [1]

  6. Nitrate ester - Wikipedia

    en.wikipedia.org/wiki/Nitrate_ester

    In organic chemistry, a nitrate ester is an organic functional group with the formula R−ONO 2, where R stands for any organyl group. They are the esters of nitric acid and alcohols . A well-known example is nitroglycerin , which is not a nitro compound, despite its name.

  7. Pentaerythritol - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol

    Pentaerythritol was first reported in 1891 by German chemist Bernhard Tollens and his student P. Wigand. [5] It may be prepared via a base-catalyzed multiple-addition reaction between acetaldehyde and 3 equivalents of formaldehyde to give pentaerythrose (CAS: 3818-32-4), followed by a Cannizzaro reaction with a fourth equivalent of formaldehyde to give the final product plus formate ion.

  8. Ethyl nitrite - Wikipedia

    en.wikipedia.org/wiki/Ethyl_nitrite

    Methemoglobinemia is the primary toxic effect of ethyl nitrite. [5] Due to ethyl nitrite's high volatility and faint smell, in the presence of ethyl nitrite vapors, it is easy to breath a high dose of it without realizing, resulting in methemoglobinemia, [ 6 ] which may or may not be severe, or even fatal .

  9. Copper compounds - Wikipedia

    en.wikipedia.org/wiki/Copper_compounds

    Many other oxyanions form complexes; these include copper(II) acetate, copper(II) nitrate, and copper(II) carbonate. Copper(II) sulfate forms a blue crystalline pentahydrate, the most familiar copper compound in the laboratory. It is used in a fungicide called the Bordeaux mixture. [3]