Names | |
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Preferred IUPAC name
Lead(II) 2,4,6-trinitrobenzene-1,3-bis(olate)
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Other names
Lead 2,4,6-trinitrobenzene-1,3-diolate
Lead 2,4,6-trinitro-m-phenylene dioxide 1,3-Benzenediol, 2,4,6-trinitro-, lead(2+) salt (1:1) Lead tricinate Lead trinitroresorcinate Tricinat |
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Identifiers | |
15245-44-0 | |
3D model (Jmol) | Interactive image |
ChemSpider | 55674 |
ECHA InfoCard | 100.035.703 |
EC Number | 239-290-0 |
PubChem | 61789 |
UN number | 0130 |
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Properties | |
C6HN3O8Pb | |
Molar mass | 450.288 g/mol |
Density | 3.06 to 3.1 g cm−3 |
Explosive data | |
Shock sensitivity | High |
Friction sensitivity | High |
Detonation velocity | 5200 m/s |
Hazards | |
Safety data sheet | Oxford MSDS |
EU classification (DSD)
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Harmful (X), Dangerous for the environment (N), Explosive (E) |
NFPA 704 | |
330 °C (626 °F; 603 K) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|
Infobox references | |
Lead styphnate (lead 2,4,6-trinitroresorcinate, C6HN3O8Pb ), whose name is derived from styphnic acid, is an explosive used as a component in primer and detonator mixtures for less sensitive secondary explosives. Lead styphnate is only slightly soluble in water and methyl alcohol Samples of lead styphnate vary in color from yellow to gold, orange, reddish-brown, to brown. Lead styphnate is known in various polymorphs, hydrates, and basic salts. Normal lead styphnate monohydrate, monobasic lead styphnate, tribasic lead styphnate dihydrate, and pentabasic lead styphnate dehydrate as well as α, β polymorphs of lead styphnate exist.
Two forms of lead styphnate are six-sided monohydrate crystals and small rectangular crystals. Lead styphnate is particularly sensitive to fire and the discharge of static electricity. When dry, it can readily detonate by static discharges from the human body. The longer and narrower the crystals, the more susceptible lead styphnate is to static electricity. Lead styphnate does not react with metals and is less sensitive to shock and friction than mercury fulminate or lead azide. It is stable in storage, even at elevated temperatures. As with other lead-containing compounds, lead styphnate is toxic owing to heavy metal poisoning.
Although never substantiated, lead styphnate may have been discovered by Peter Griess (of Griess test fame) in 1874. In 1919, Edmund Herz first established a preparation of anhydrous normal lead styphnate by the reaction of magnesium styphnate with lead acetate in the presence of nitric acid.
Normal lead styphnate exists as α and β polymorphs, both being monoclinic crystals. The lead centres are seven-coordinate and are bridged via oxygen bridges. The water molecule is coordinated to the metal and is also hydrogen-bonded to the anion. Many of the Pb-O distances are short, indicating some degree of covalency. The styphnate ions lie in approximately parallel planes linked by Pb atoms.