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・ Erythrina tahitensis
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Erythritol tetranitrate
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Erythritol tetranitrate : ウィキペディア英語版
Erythritol tetranitrate

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Erythritol tetranitrate (ETN) is an explosive compound chemically similar to PETN.〔Erythritol tetranitrate was first synthesized by British chemist John Stenhouse (1809-1880) in 1849. He extracted the simple sugar erythritol (which he called "erythroglucin") from lichen and then studied its chemistry. See: John Stenhouse (1 January 1849) "Examination of the proximate principles of some of the lichens. Part II," ''Philosophical Transactions of the Royal Society (London)'', vol. 139, pages 393-401. Reprinted in German as: John von Stenhouse (1849) "Über die näheren Bestandtheile einige Flechten," Justus Liebigs ''Annalen der Chemie und Pharmacie'', vol. 70, no. 2, pages 218-228. Condensed version (in German): John Stenhouse (12 Sept. 1849) "Über die näheren Bestandtheile einige Flechten," ''Pharmaceutisches Centralblatt'', vol. 20, no. 40, (pages 625-628 ).〕 It is however thought to be 1/3 more sensitive to friction and impact. ETN is not well known, but in recent years has been used by amateur experimenters to replace PETN in improvised detonation cord or in boosters to initiate larger, less sensitive explosive charges. Due to the availability of erythritol as a natural sweetener and its relative ease of production in relation to PETN, ETN is a favoured homemade explosive compound to the amateur experimenter.
Like many nitrate esters, ETN acts as a vasodilator, and was the active ingredient in the original "sustained release" tablets, made under a process patent in the early 50s, called "nitroglyn". Ingesting ETN or prolonged skin contact can lead to absorption and what is known as a "nitro headache".
==Properties==
ETN has a relatively high velocity of detonation of 8000–8100 m/s at a density of 1.6 g/cm3. It is white in color and odorless. ETN is commonly cast into mixtures with other high explosives. It is somewhat sensitive to shock and friction, so care should be taken while handling. ETN dissolves readily in acetone and other ketone solvents.
Much like PETN, ETN is known for having a very long shelf life. Studies that directly observed the crystalline structure saw no signs of decomposition after four years of storage at room temperature.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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