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Common molecules sample 50747 - Reciprocal Net Log in
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Empirical formula: C6H3N3O7
a: 9.254 Å
b: 19.127 Å
c: 9.704 Å
α (alpha): 90.00 °
β (beta): 90.00 °
γ (gamma): 90.00 °
Volume: 1717.62 Å3
Space group: Pca21
Calculated density: 1.772 g/cm3
Z: 8
Temperature: 22.0 °C
Formula weight: 229.106 g/mole
R(F): 0.0510
Common name: Picric acid
CSD refcode: PICRAC
Short description: Picric acid, or trinitrophenol, is a highly reactive, toxic compound used in the manufacture of dyes and high-powered explosives
Keyword: toxic
Keyword: inert dyes
Keyword: explosive
IUPAC name: 2,4,6-Trinitrophenol
Layman's explanation: Picric Acid was first discovered in 1771 by a British Chemist named Peter Woulfe by treatment of indigo with nitric acid. It is most commonly seen in its yellow, water-soluble, crystalline form. For this reason, picric acid first saw use as a dyeing agent in textiles. However, around 1849 it was discovered (for obvious reasons) that picric acid is a shock, heat, and friction-sensitive explosive. Its first use as an explosive material came in military weaponry: torpedoes in particular due to its shock-sensitive nature not requiring a detonator to explode on contact with a target. However, picric acid was found to be highly corrosive to metals, making the weapons very difficult to handle and the acid itself difficult to store. Today, picric acid is used more widely as an ingredient in the manufacture of inert dyes and stable explosives such as dynamite.
Citation of a publication: E.N.Duesler, J.H.Engelmann, D.Y.Curtin, I.C.Paul; Cryst.Struct.Commun., 7, (1978), 449
Lab name: Common molecules
Sample provider: Obtained courtesy of the Cambridge Structural Database
Status: Complete, visible to public
Repository Files:
50747.cif 50747.crt 50747.gif 50747.GIF 50747.ort
50747.pdb 50747.sdt 50747f.crt 50747f.pdb 50747f.sdt

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