1,3,5-Trinitrobenzene

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1,3,5-Trinitrobenzene[1]
Skeletal formula
Ball-and-stick model
Identifiers
CAS number 99-35-4 YesY
PubChem 7434
ChemSpider 7156 YesY
UN number 0388
Jmol-3D images Image 1
Properties
Molecular formula C6H3N3O6
Molar mass 213.10 g mol−1
Density 1.76 g/cm3
Melting point 123.2 °C (253.8 °F; 396.3 K)
Boiling point 315 °C (599 °F; 588 K)
Solubility in water 330 mg/L
Hazards
NFPA 704
Flammability code 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g., propane Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 4: Readily capable of detonation or explosive decomposition at normal temperatures and pressures. E.g., nitroglycerin Special hazards (white): no codeNFPA 704 four-colored diamond
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 YesY (verify) (what is: YesY/N?)
Infobox references

1,3,5-Trinitrobenzene is a nitrated benzene-derivative that is classified as a high explosive, being moderately explosive in liquid form and extremely explosive in its dry powder form. It has a clear to light yellow sludgy appearance. It will detonate under strong shock. High temperatures, whether by sudden heating of any quantity, or by the accumulation of heat when large quantities are burning, will also cause detonation. The material can react vigorously with reducing materials and is incompatible with sodium dichromate or sulfuric acid.[2] It must be stored in a cool, ventilated place, away from acute fire hazards and easily oxidized materials. It also reacts violently with aluminium, boron phosphide, cyanides, esters, PN2H, phosphorus, NaCN, SnC12, sodium hypophosphite, thiocyanates, etc. When heated to decomposition it emits highly toxic fumes of NOx. It is an extremely powerful oxidizing agent which may cause violent reaction with reducing materials.[3]

Uses and applications[edit]

Trinitrobenzene is used primarily as a high explosive for commercial mining and military use. Some other uses include a narrow-range pH indicator, an agent to vulcanize natural rubber, and a mediating agent to mediate the synthesis of other explosive compounds.[4]

Safety Precautions[edit]

It is recommended that people avoid contact if possible. Avoid breathing dusts, and fumes from burning or reacting material. Wear appropriate chemical protective gloves and goggles. Do not handle broken packages unless wearing appropriate personal protective equipment. Wash away any material which may have contacted the body with copious amounts of water or soap and water. Do not store near other chemicals (especially other oxidizers), near sources of heating, or places where rapid temperature changes may occur. In case of spillage immediately soak with water and carefully and slowly clean up. In case of fire let burn; DO NOT attempt to put out the resulting fire. In any case where the compound is ingested call Poison Control Center immediately.[5]

Health problems[edit]

The most common modes of exposure are either direct contact with the substance or through drinking contaminated water. 1,3,5-Trinitrobenzene is believed to cause similar health problems as TNT. Exposure to high concentrations most commonly causes anemia, or the reduced ability for blood to carry oxygen. As a result of the lack of oxygen, the skin typically becomes blue or purple in color. Other symptoms of exposure include headache, nausea, and dizziness. The long term effects from exposure are not known because no long term studies of health effects have been performed. It is believed that long term exposure will cause sterility (especially in males) and cataracts. It is unknown if Trinitrobenzene causes birth defects or cancer.[6]

See also[edit]

References[edit]

  1. ^ Record of 1,3,5-Trinitrobenzene in the GESTIS Substance Database from the IFA
  2. ^ (Sax and Lewis, 1987) p.839.
  3. ^ (SAX and Lewis, 1987) p.664.
  4. ^ John Pike (1997-05-21). "Explosives - Nitroaromatics". Globalsecurity.org. Retrieved 2013-10-28. 
  5. ^ "TRINITROTOLUENE (TNT) AND TRINITROBENZENE MIXTURES [OR] TRINITROTOLUENE (TNT) AND HEXANITROSTILBENE MIXTURES". CAMEO Chemicals (Chemical Datasheet). National Oceanic and Atmospheric Administration. Archived from the original on May 28, 2010. 
  6. ^ "ATSDR - Redirect - ToxFAQs™: 1,3-Dinitrobenzene and 1,3,5-Trinitrobenzene". Atsdr.cdc.gov. 2010-07-20. Retrieved 2013-10-28.