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4-Chloroaniline

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Chemical compound
4-Chloroaniline
Names
Preferred IUPAC name 4-Chloroaniline
Systematic IUPAC name 4-Chlorobenzenamine
Other names p-Chloroaniline
Identifiers
CAS Number
3D model (JSmol)
Beilstein Reference 471359
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.093 Edit this at Wikidata
KEGG
PubChem CID
RTECS number
  • BX0700000
UNII
UN number 2018
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C6H6ClN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2Key: QSNSCYSYFYORTR-UHFFFAOYSA-N
SMILES
  • C1=CC(=CC=C1N)Cl
Properties
Chemical formula ClC6H4NH2
Appearance Pale yellow solid
Density 1.43 g/cm
Melting point 72.5 °C (162.5 °F; 345.6 K)
Boiling point 232 °C (450 °F; 505 K)
Solubility in water 2.6 g/L at 20 °C
Hazards
Occupational safety and health (OHS/OSH):
Main hazards Very toxic, possible carcinogen. Absorbed through skin.
GHS labelling:
Pictograms GHS06: ToxicGHS07: Exclamation markGHS08: Health hazardGHS09: Environmental hazard
Signal word Danger
Hazard statements H301, H311, H317, H331, H350, H400
Precautionary statements P201, P202, P261, P264, P270, P271, P272, P273, P280, P281, P301+P310, P302+P352, P304+P340, P308+P313, P311, P312, P321, P322, P330, P333+P313, P361, P363, P391, P403+P233, P405, P501
Flash point 113 °C (235 °F; 386 K)
Safety data sheet (SDS) External MSDS
Related compounds
Related compounds 2,4,6-Trichloroaniline
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

4-Chloroaniline is an organochlorine compound with the formula ClC6H4NH2. This pale yellow solid is one of the three isomers of chloroaniline.

Preparation

4-Chloroaniline is not prepared from aniline, which tends to overchlorinate. Instead, it is prepared by reduction of 4-nitrochlorobenzene, which in turn is prepared by nitration of chlorobenzene.

Uses

4-Chloroaniline is used in the industrial production of pesticides, drugs, and dyestuffs. It is a precursor to the widely used antimicrobial and bacteriocide chlorhexidine and is used in the manufacture of pesticides, including pyraclostrobin, anilofos, monolinuron, and chlorphthalim.

4-Chloroaniline exhibits antimicrobial action against some bacteria and molds.

References

  1. ^ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 669. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
  2. Scheunert, 1981
  3. "Safety data for 4-chloroaniline". Oxford University. Archived from the original on 2012-04-23. Retrieved 2008-03-11.
  4. ^ Gerald Booth (2007). "Nitro Compounds, Aromatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_411. ISBN 9783527303854.
  5. Ashford's Dictionary of Industrial Chemicals (3rd ed.). 2011. p. 1998.
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