Dinitrobenzene - Wikipedia

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Appearance move to sidebar hide From Wikipedia, the free encyclopedia Class of compounds

Dinitrobenzenes are nitrobenzenes composed of a benzene ring and two nitro group (-NO2) substituents. The three possible arrangements of the nitro groups afford three isomers, 1,2-dinitrobenzene, 1,3-dinitrobenzene, and 1,4-dinitrobenzene. Each isomer has the chemical formula C6H4N2O4 and a molar mass of about 168.11 g/mol. 1,3-Dinitrobenzene is the most common isomer and it is used in the manufacture of explosives.

Properties

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The dinitrobenzenes are all crystalline solids. The boiling points of the three isomers are relatively close; however, the melting points significantly differ. 1,4-Dinitrobenzene, which has the highest symmetry, has the highest melting point.

Dinitrobenzenes
IUPAC name 1,2-Dinitrobenzene 1,3-Dinitrobenzene 1,4-Dinitrobenzene
Other names o-Dinitrobenzene m-Dinitrobenzene p-Dinitrobenzene
Chemical structure
CAS number 528-29-0 99-65-0 100-25-4
25154-54-5 (Unspecified isomers)[1]
PubChem CID 10707 from PubChem CID 7452 from PubChem CID 7492 from PubChem
Chemical formula C6H4N2O4
Molar mass 168.11 g/mol
Magnetic Susceptibility -65.98·10−6 cm3/mol -70.53·10−6 cm3/mol -68.30·10−6 cm3/mol
Physical state solid
Appearance white solid yellowish solid pale yellow solid[2]
Melting point 118 °C[3] 89.6 °C[4] 174 °C[5]
Boiling point 318 °C[3] 297 °C[4] 299 °C[6]
Density 1.565 g/cm3 (17 °C)[6] 1.575 g/cm3 (18 °C)[6] 1.625 g/cm3 (18 °C)[6]
Vapor pressure 0.08 Pa (30 °C)[7] 0.07 Pa (30 °C)[7]
0.34 Pa (50 °C)[7] 0.23 Pa (50 °C)[7]
Solubility Insoluble in water
GHS hazards[8]
H phrases H300, H310, H330, H373, H410
P phrases P260, P262, P264, P270, P271, P273, P280, P284, P301+P310, P302+P350, P304+P340, P310, P314, P320, P321, P322, P330, P361, P363, P391, P403+P233, P405, P501

References

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  1. ^ Record of CAS RN 25154-54-5 in the GESTIS Substance Database of the Institute for Occupational Safety and Health
  2. ^ E. B. Starkey (1939). "P-DINITROBENZENE". Organic Syntheses. 19: 40. doi:10.15227/orgsyn.019.0040.
  3. ^ a b Record of CAS RN 528-29-0 in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 11 March 2008.
  4. ^ a b Record of CAS RN 99-65-0 in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 11 March 2008.
  5. ^ Record of CAS RN 100-25-4 in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 11 March 2008.
  6. ^ a b c d Brockhaus ABC Chemie, VEB F.A. Brockhaus Verlag, Leipzig 1971.
  7. ^ a b c d Félix-Rivera, Hilsamar (2011). "Triacetone triperoxide thermogravimetric study of vapor pressure and enthalpy of sublimation in 303–338K temperature range". Thermochimica Acta. 514 (1–2): 37–43. doi:10.1016/j.tca.2010.11.034.)
  8. ^ "Globally Harmonized System of Classification and Labelling of Chemicals" (pdf). 2021. Annex 3: Codification of Statements and Pictograms (pp 268–385).
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