Nitroglycerin: Difference between revisions
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'''Nitroglycerin''' is a very unstable [[high-explosive]]. Its chemical composition is propane-1,2,3-triyl trinitrate, a [[glycerol]] molecule with three nitro groups substituents on the hydroxy groups. | '''Nitroglycerin''' is a very unstable [[high-explosive]]. Its chemical composition is propane-1,2,3-triyl trinitrate, a [[glycerol]] molecule with three nitro groups substituents on the hydroxy groups. | ||
As a young man, the scientist and inventor [[Alfred Nobel]] (1833-1896) [http://nobelprize.org/alfred_nobel/biographical/articles/life-work/index.html] | |||
chemical engineering visited the Paris laboratory of a famous chemist, Professor T. J. Pelouze. There, he met Ascanio Sobrero who, three years earlier, had invented nitroglycerin. Nitroglycerin was then thought much too dangerous to be useful, despite its considerable explosive power, but Nobel became interested in how nitroglycerine might be made safe to handle. Back in his home of Stockholm, he began experiments with his father, but several explosions, including one in 1864 that killed his brother Emil led the authorities that to ban any further experiments within the Stockholm city limits. However, Nobel was not discouraged, he moved his experiments to a barge anchored on Lake Mälaren, and soon began mass production of nitroglycerin. He found that mixing nitroglycerin with a clay (kieselguhr) produced a paste which could be shaped into rods that could be handled and stored relatively safely, and which were suitable for insertion into drilling holes. In 1867, he patented this material, calling it ''dynamite''. | |||
==Medical uses== | ==Medical uses== |
Revision as of 09:40, 5 September 2007
Nitroglycerin is a very unstable high-explosive. Its chemical composition is propane-1,2,3-triyl trinitrate, a glycerol molecule with three nitro groups substituents on the hydroxy groups.
As a young man, the scientist and inventor Alfred Nobel (1833-1896) [1] chemical engineering visited the Paris laboratory of a famous chemist, Professor T. J. Pelouze. There, he met Ascanio Sobrero who, three years earlier, had invented nitroglycerin. Nitroglycerin was then thought much too dangerous to be useful, despite its considerable explosive power, but Nobel became interested in how nitroglycerine might be made safe to handle. Back in his home of Stockholm, he began experiments with his father, but several explosions, including one in 1864 that killed his brother Emil led the authorities that to ban any further experiments within the Stockholm city limits. However, Nobel was not discouraged, he moved his experiments to a barge anchored on Lake Mälaren, and soon began mass production of nitroglycerin. He found that mixing nitroglycerin with a clay (kieselguhr) produced a paste which could be shaped into rods that could be handled and stored relatively safely, and which were suitable for insertion into drilling holes. In 1867, he patented this material, calling it dynamite.
Medical uses
Nitroglycerin is used to treat chest pain (angina), and can also be used with other drugs to treat congestive heart failure and heart attacks. It works by relaxing the blood vessels to the heart (vasodilation, thereby increasing the blood flow and oxygen supply to the heart. Nitroglycerin can thus reduce chest pain but it does not cure the underlying causes.
Nitroglycerin (as a medicine) comes in the form of a sublingual tablet, buccal tablet, extended-release (long-acting) capsule, or oral spray. The extended-release formulations are usually taken 3-6 times a day to treat chronic or frequently recurring chest pain. The sublingual tablet and spray are used to relieve acute chest pain that has already started, or to prevent pain before activities that are known to provoke attacks (e.g., exercise or cold weather). Common side-effects include headache, rash, dizziness, upset stomach and flushing (feeling of warmth). [2]
Brand names
Nitro-Bid® Nitrogard® Nitroglycerin Slocaps® Nitrolingual® Pumpspray NitroQuick® Nitrostat® Nitrotab® Nitro-Time®