Pentachloroaniline

Last updated
Pentachloroaniline
Pentachloroaniline.svg
Names
Preferred IUPAC name
2,3,4,5,6-pentachloroaniline
Other names
Benzenamine, pentachloroaminobenzene [1]
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.007.647 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 208-410-3
PubChem CID
UNII
  • InChI=1S/C6H2Cl5N/c7-1-2(8)4(10)6(12)5(11)3(1)9/h12H2
    Key: KHCZSJXTDDHLGJ-UHFFFAOYSA-N
  • C1(=C(C(=C(C(=C1Cl)Cl)Cl)Cl)Cl)N
Properties
C6H2Cl5N
Molar mass 265.34 g·mol−1
Appearanceyellow crystalline solid
Density 1.75 g/cm³
Melting point −43.8 °C (−46.8 °F; 229.3 K)
Boiling point 81.6 °C (178.9 °F; 354.8 K)
practically insoluble
Hazards
GHS labelling:
GHS-pictogram-exclam.svg GHS-pictogram-flamme.svg [2]
Danger
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Pentachlorotoluene is a chemical compound from the group of chloroanilines. Its chemical formula is C6H2Cl5N. [3] Pentachloroaniline occurs as a derivative of pentachloronitrobenzene. [4] [5]

Contents

Synthesis

Pentachloroaniline can be obtained by reducing pentachloronitrobenzene with tin, hydrochloric acid, and ethanol. It is also formed by the action of chlorine on an ethereal solution of symmetrical m-dichloroaniline. [6]

Physical characteristics

Pentachloroaniline is a yellow crystalline solid, practically insoluble in water, but readily dissolves in organic solvents. Highly flammable.

Uses

Pentachloroaniline is highly important in the industrial field, where it is utilized in various ways. Belonging to the aniline group, which comprises substances such as aniline and chloroanilines, it is employed as a dye and as an intermediate in the synthesis of plasticizers and pesticides. Additionally, it is involved in rubber production and functions as a flame retardant. [7]

See also

References

  1. Informatics, NIST Office of Data and. "2,3,4,5,6-Pentachloroaniline". webbook.nist.gov. Retrieved 23 April 2025.
  2. "Pentachloroaniline". accustandard.com. Retrieved 23 April 2025.
  3. "NCATS Inxight Drugs — PENTACHLOROANILINE". drugs.ncats.io. Retrieved 23 April 2025.
  4. "Pentachloroaniline". sitem.herts.ac.uk. Retrieved 23 April 2025.
  5. "Pentachloroaniline". Sigma Aldrich . Retrieved 23 April 2025.
  6. Erlenmeyer, Emil (1894). Lehrbuch der organischen Chemie (in German). C.F. Winter'sche Verlagshandlung. p. 743. Retrieved 23 April 2025.
  7. "Pentachloroaniline | CAS 527-20-8 | SCBT - Santa Cruz Biotechnology". scbt.com . Retrieved 23 April 2025.