Nitrobenzene

Nitrobenzene is an organic compound with the chemical formula C6H5NO2. It is a water-insoluble pale yellow oil with an almond-like odor. It freezes to give greenish-yellow crystals. It is produced on a large scale from benzene as a precursor to aniline. In the laboratory, it is occasionally used as a solvent, especially for electrophilic reagents.

Nitrobenzene
Nitrobenzene
Nitrobenzene
Nitrobenzene
Nitrobenzene
Names
Preferred IUPAC name
Nitrobenzene
Other names
Nitrobenzol
Nitritebenzene
Oil of mirbane
Identifiers
3D model (JSmol)
507540
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.002.469
EC Number
  • 202-716-0
50357
KEGG
RTECS number
  • DA6475000
UNII
  • InChI=1S/C6H5NO2/c8-7(9)6-4-2-1-3-5-6/h1-5H checkY
    Key: LQNUZADURLCDLV-UHFFFAOYSA-N checkY
  • InChI=1/C6H5NO2/c8-7(9)6-4-2-1-3-5-6/h1-5H
    Key: LQNUZADURLCDLV-UHFFFAOYAA
  • c1ccc(cc1)[N+](=O)[O-]
Properties
C6H5NO2
Molar mass 123.11 g/mol
Appearance yellowish, oily liquid[1]
Odor pungent, like paste shoe polish[1]
Density 1.199 g/cm3
Melting point 5.7 °C (42.3 °F; 278.8 K)
Boiling point 210.9 °C (411.6 °F; 484.0 K)
0.19 g/100 ml at 20 °C
Vapor pressure 0.3 mmHg (25°C)[1]
-61.80·10−6 cm3/mol
Viscosity 1.8112 mPa·s[2]
Hazards
GHS labelling:
GHS06: ToxicGHS08: Health hazard
Danger
H301, H311, H331, H351, H360, H372, H412
P201, P202, P260, P261, P264, P270, P271, P273, P280, P281, P301+P310, P302+P352, P304+P340, P308+P313, P311, P312, P314, P321, P322, P330, P361, P363, P403+P233, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamond
3
2
1
Flash point 88 °C (190 °F; 361 K)
480 °C (896 °F; 753 K)
Explosive limits 1.8%-?[1]
Lethal dose or concentration (LD, LC):
780 mg/kg (rat, oral)
600 mg/kg (rat, oral)
590 mg/kg (mouse, oral)
[3]
750 mg/kg (dog, oral)[3]
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 1 ppm (5 mg/m3) [skin][1]
REL (Recommended)
 TWA 1 ppm (5 mg/m3) [skin][1]
IDLH (Immediate danger)
 200 ppm[1]
Related compounds
Related compounds
 Aniline
Benzenediazonium chloride
Nitrosobenzene
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 ?)
Infobox references

Production

Nitrobenzene is prepared by nitration of benzene with a mixture of concentrated sulfuric acid, water, and nitric acid. This mixture is sometimes called "mixed acid." The production of nitrobenzene is one of the most dangerous processes conducted in the chemical industry because of the exothermicity of the reaction (ΔH = −117 kJ/mol).[4]

+
 
 H+
Rightward reaction arrow with minor product(s) to top right

World capacity for nitrobenzene in 1985 was about 1,700,000 tonnes.[4]

The nitration process involves formation of the nitronium ion (NO2+), followed by an electrophilic aromatic substitution reaction of it with benzene. The nitronium ion is generated by the reaction of nitric acid and an acidic dehydration agent, typically sulfuric acid:

HNO3 + H+ ⇌ NO2+ + H2O

Uses

Approximately 95% of nitrobenzene industrially produced is hydrogenated to aniline:[4]

C6H5NO2 + 3 H2 → C6H5NH2 + 2 H2O

Aniline is a precursor to urethane polymers, rubber chemicals, pesticides, dyes (particularly azo dyes), explosives, and pharmaceuticals.

Most aniline is consumed in the production of methylenedianiline, a precursor to polyurethanes.

Specialized applications

Nitrobenzene is also used to mask unpleasant odors in shoe and floor polishes, leather dressings, paint solvents, and other materials. Redistilled, as oil of mirbane, nitrobenzene had been used as an inexpensive perfume for soaps. It has been replaced by less toxic chemicals for this purpose.[5] A significant merchant market for nitrobenzene is its use in the production of the analgesic paracetamol (also known as acetaminophen) (Mannsville 1991).[6] Nitrobenzene is also used in Kerr cells, as it has an unusually large Kerr constant. Evidence suggests its use in agriculture as a plant growth/flowering stimulant.[7]

Organic reactions

Aside from its conversion to aniline, nitrobenzene can be selectively reduced to azoxybenzene,[8] azobenzene,[9] nitrosobenzene,[10] hydrazobenzene,[11] and phenylhydroxylamine.[12] It has been used as a mild oxidant in reactions like the Skraup quinoline synthesis.[13]

Safety

Nitrobenzene is highly toxic (Threshold Limit Value 5 mg/m3) and readily absorbed through the skin.

Prolonged exposure may cause serious damage to the central nervous system, impair vision, cause liver or kidney damage, anemia and lung irritation. Inhalation of vapors may induce headache, nausea, fatigue, dizziness, cyanosis, weakness in the arms and legs, and in rare cases may be fatal. The oil is readily absorbed through the skin and may increase heart rate, cause convulsions or rarely death. Ingestion may similarly cause headaches, dizziness, nausea, vomiting and gastrointestinal irritation, loss of sensation/use in limbs and also causes internal bleeding.[10]

Nitrobenzene is considered a likely human carcinogen by the United States Environmental Protection Agency,[14] and is classified by the IARC as a Group 2B carcinogen which is "possibly carcinogenic to humans".[15] It has been shown to cause liver, kidney, and thyroid adenomas and carcinomas in rats.[16]

It is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities.[17]

References
  1. NIOSH Pocket Guide to Chemical Hazards. "#0450". National Institute for Occupational Safety and Health (NIOSH).
  2. Ahluwalia, R.; Wanchoo, R. K.; Sharma, S. K.; Vashisht, J. L. (1996). "Density, viscosity, and surface tension of binary liquid systems: Ethanoic acid, propanoic acid, and butanoic acid with nitrobenzene". Journal of Solution Chemistry. 25 (9): 905–917. doi:10.1007/BF00972581. ISSN 0095-9782. S2CID 95126469.
  3. "Nitrobenzene". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  4. Booth G (2007). "Nitro Compounds, Aromatic". Ullmann's Encyclopedia of Industrial Chemistry (6th ed.). Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_411. ISBN 978-3-527-30385-4.
  5. Hogarth CW (January 1912). "a case of poisoning by oil of mirbane (nitro-benzol)". British Medical Journal. 1 (2665): 183. doi:10.1136/bmj.1.2665.183. PMC 2344391. PMID 20765985.
  6. Bhattacharya A, Purohit VC, Suarez V, Tichkule R, Parmer G, Rinaldi F (March 2006). "One-step reductive amidation of nitro arenes: application in the synthesis of Acetaminophen". Tetrahedron Letters. 47 (11): 1861–1864. doi:10.1016/j.tetlet.2005.09.196.
  7. "Flowering stimulant composition using nitrobenzene".
  8. Bigelow, H. E.; Palmer, Albert. "Azoxybenzene". Organic Syntheses.; Collective Volume, vol. 2, 1943, p. 57
  9. Bigelow HE, Robinson DB (1955). "Azobenzene". Organic Syntheses.; Collective Volume, vol. 3, p. 103
  10. Coleman GH, McCloskey CM, Stuart FA. "Nitrosobenzene". Organic Syntheses.; Collective Volume, vol. 3, p. 668
  11. Karwa, Shrikant L.; Rajadhyaksha, Rajeev A. (January 1988). "Selective catalytic hydrogenation of nitrobenzene to hydrazobenzene". Industrial & Engineering Chemistry Research. 27 (1): 21–24. doi:10.1021/ie00073a005. ISSN 0888-5885.
  12. Kamm O. "β-Phenylhydroxylamine". Organic Syntheses.; Collective Volume, vol. 1, p. 445
  13. Clarke, HT; Davis, AW. "Quinoline". Organic Syntheses. 1: 478.
  14. Division, US EPA, ORD, Integrated Risk Information System. "Nitrobenzene CASRN 98-95-3 - IRIS - US EPA, ORD". cfpub.epa.gov. Retrieved 10 August 2017.{{cite web}}: CS1 maint: multiple names: authors list (link)
  15. "Agents Classified by the IARC Monographs, International Agency for Research on Cancer" (PDF). Retrieved 10 August 2017.
  16. National Institutes of Health · U.S. Department of Health and Human Services, Nomination: Nitrobenzene Review committee, 02/02/2010
  17. "40 C.F.R.: Appendix A to Part 355—The List of Extremely Hazardous Substances and Their Threshold Planning Quantities" (PDF) (July 1, 2008 ed.). Government Printing Office. Archived from the original (PDF) on February 25, 2012. Retrieved October 29, 2011. {{cite journal}}: Cite journal requires |journal= (help)
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