Nitrobenzene Explained

Nitrobenzene is an aromatic nitro compound and the simplest of the nitrobenzenes, 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.

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).

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

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:[1]

C6H5NO2 + 3 H2 → C6H5NH2 + 2 H2OAniline is a precursor to urethane polymers, rubber chemicals, pesticides, dyes (particularly azo dyes), explosives, and pharmaceuticals.

Specialized applications

Nitrobenzene is 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 It has been replaced by less toxic chemicals for this purpose.[2] A significant merchant market for nitrobenzene is its use in the production of the analgesic paracetamol (also known as acetaminophen).[3] 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.[4]

Organic reactions

Aside from its conversion to aniline, nitrobenzene can be selectively reduced to azoxybenzene,[5] azobenzene, nitrosobenzene, hydrazobenzene,[6] and phenylhydroxylamine. It has been used as a mild oxidant in reactions like the Skraup quinoline synthesis.[7]

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.

Nitrobenzene is considered a likely human carcinogen by the United States Environmental Protection Agency,[8] and is classified by the IARC as a Group 2B carcinogen which is "possibly carcinogenic to humans".[9] It has been shown to cause liver, kidney, and thyroid adenomas and carcinomas in rats.[10]

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.[11]

External links

Notes and References

  1. Book: Booth, Gerald . vanc . Nitro Compounds, Aromatic . Ullmann's Encyclopedia of Industrial Chemistry . 2007 . Wiley-VCH . Weinheim . 978-3-527-30385-4 . 10.1002/14356007.a17_411 . 6th.
  2. Hogarth CW . a case of poisoning by oil of mirbane (nitro-benzol) . British Medical Journal . 1 . 2665 . 183 . January 1912 . 20765985 . 2344391 . 10.1136/bmj.1.2665.183.
  3. Bhattacharya . Apurba . Purohit . Vikram C. . Suarez . Victor . Tichkule . Ritesh . Parmer . Gaurang . Rinaldi . Frank . vanc . One-step reductive amidation of nitro arenes: application in the synthesis of Acetaminophen . Tetrahedron Letters . March 2006 . 47 . 11 . 1861–1864 . 10.1016/j.tetlet.2005.09.196.
  4. Web site: Flowering stimulant composition using nitrobenzene.
  5. Bigelow. H. E.. Palmer. Albert . Azoxybenzene . Organic Syntheses . 1931 . 11 . 16 . 10.15227/orgsyn.011.0016.
  6. Karwa. Shrikant L.. Rajadhyaksha. Rajeev A.. January 1988. Selective catalytic hydrogenation of nitrobenzene to hydrazobenzene. Industrial & Engineering Chemistry Research. EN. 27. 1. 21–24. 10.1021/ie00073a005. 0888-5885.
  7. Clarke. HT. Davis. AW. Quinoline. Organic Syntheses. 1. 478.
  8. Web site: Nitrobenzene CASRN 98-95-3 - IRIS - US EPA, ORD. US EPA, ORD, Integrated Risk Information System. Division. cfpub.epa.gov. 10 August 2017.
  9. Web site: Agents Classified by the IARC Monographs, International Agency for Research on Cancer. 10 August 2017.
  10. National Institutes of Health · U.S. Department of Health and Human Services, Nomination: Nitrobenzene Review committee, 02/02/2010
  11. Web site: . 40 C.F.R.: Appendix A to Part 355—The List of Extremely Hazardous Substances and Their Threshold Planning Quantities . July 1, 2008 . October 29, 2011 . https://web.archive.org/web/20120225051612/http://edocket.access.gpo.gov/cfr_2008/julqtr/pdf/40cfr355AppA.pdf . February 25, 2012 . dead .