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Styphnic acid

From Wikipedia, the free encyclopedia

Styphnic acid
Styphnic acid
Names
Preferred IUPAC name
2,4,6-Trinitrobenzene-1,3-diol
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.001.306 Edit this at Wikidata
UNII
UN number 0219 – Dry or wetted with < 20% water/alcohol
0394 – Wetted with >= 20% water/alcohol
  • InChI=1S/C6H3N3O8/c10-5-2(7(12)13)1-3(8(14)15)6(11)4(5)9(16)17/h1,10-11H checkY
    Key: IXHMHWIBCIYOAZ-UHFFFAOYSA-N checkY
  • InChI=1/C6H3N3O8/c10-5-2(7(12)13)1-3(8(14)15)6(11)4(5)9(16)17/h1,10-11H
    Key: IXHMHWIBCIYOAZ-UHFFFAOYAQ
  • c1c(c(c(c(c1[N+](=O)[O-])O)[N+](=O)[O-])O)[N+](=O)[O-]
Properties
C6H3N3O8
Molar mass 245.11 g/mol
Density 1.829 g/cm3
Melting point 180 °C (356 °F; 453 K)
Boiling point decomposes
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Styphnic acid (from Greek stryphnos "astringent"[1]), or 2,4,6-trinitro-1,3-benzenediol, is a yellow astringent acid that forms hexagonal crystals. It is used in the manufacture of dyes, pigments, inks, medicines, and explosives such as lead styphnate. It is itself a low-sensitivity explosive, similar to picric acid, but explodes upon rapid heating.[2]

YouTube Encyclopedic

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  • Carboxylation of resorcinol
  • Lead Styphnate detonation

Transcription

Preparation and chemistry

It may be prepared by the nitration of resorcinol with a mixture of nitric and sulfuric acid.[3]

This compound is an example of a trinitrophenol.

Like picric acid, it is a moderately strong acid, capable of displacing carbon dioxide from solutions of sodium carbonate, for example.

It may be reacted with weakly basic oxides, such as those of lead and silver, to form the corresponding salts.

The solubility of picric acid and styphnic acid in water is less than their corresponding mono- and di-nitro compounds, and far less than their non-nitrated precursor phenols, so they may be purified by fractional crystallisation.

References

  1. ^ Alexander Senning (2006). Elsevier's Dictionary of Chemoetymology: The Whys and Whences of Chemical Nomenclature and Terminology, p. 375, at Google Books
  2. ^ Armarego, W.L.F.; Chai, C.L.L. (2003). Purification of Laboratory Chemicals. Butterworth-Heinemann. p. 353. ISBN 9780750675710. Retrieved 2015-05-20.
  3. ^ Barros, Sam. "PowerLabs Styphnic Acid Synthesis!". powerlabs.org. Retrieved 2015-05-20.
This page was last edited on 17 May 2024, at 20:20
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