3,5-Dichloroaniline

3,5-Dichloroaniline
Names
Other names
1-amino-3,5- dichlorobenzene
Identifiers
CAS Number
  • 626-43-7
3D model (JSmol)
  • Interactive image
Beilstein Reference
 636492
ChEBI
  • CHEBI:19904
ChEMBL
  • ChEMBL1451208
ChemSpider
  • 11778
ECHA InfoCard 100.009.954 Edit this at Wikidata
EC Number
  • 210-948-9
Gmelin Reference
 363409
PubChem CID
  • 12281
UNII
  • OZ75ZM1S3G
CompTox Dashboard (EPA)
  • DTXSID7030307 Edit this at Wikidata
InChI
  • InChI=1S/C6H5Cl2N/c7-4-1-5(8)3-6(9)2-4/h1-3H,9H2
    Key: UQRLKWGPEVNVHT-UHFFFAOYSA-N
  • C1=C(C=C(C=C1Cl)Cl)N
Properties
Chemical formula
 C6H5Cl2N
Molar mass 162.01 g·mol−1
Appearance colorless solid
Density 1.58 g/cm3
Melting point 51–53 °C (124–127 °F; 324–326 K)
Boiling point 260 °C (500 °F; 533 K) 741 torr
Hazards
GHS labelling:[1]
Pictograms
 GHS06: ToxicGHS08: Health hazardGHS09: Environmental hazard
Danger
Hazard statements
 H301, H311, H331, H373, H410
P260, P261, P262, P264, P270, P271, P273, P280, P301+P316, P302+P352, P304+P340, P316, P319, P321, P330, P361+P364, P391, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

3,5-Dichloroaniline is an organic compound with the formula C6H3Cl2(NH2). It is one of several isomers of dichloroaniline. It is a colorless solid although commercial samples often appear colored. It is produced by hydrogenation of 3,5-dichloronitrobenzene.[2] It is a precursor to the fungicide vinclozolin.

Safety and environmental aspects

Its 72-h EC50 in an algal growth inhibition assay is 4.39 mg/L.[3] Biodegradation of dichloroanilines usually proceeds via initial ring hydroxylation.[4]

References

  1. ^ "3,5-Dichloroaniline". pubchem.ncbi.nlm.nih.gov.
  2. ^ Jagadeesh, Rajenahally V.; Surkus, Annette-Enrica; Junge, Henrik; Pohl, Marga-Martina; Radnik, Jörg; Rabeah, Jabor; Huan, Heming; Schünemann, Volker; Brückner, Angelika; Beller, Matthias (2013). "Nanoscale Fe2O3-Based Catalysts for Selective Hydrogenation of Nitroarenes to Anilines". Science. 342 (6162): 1073–1076. Bibcode:2013Sci...342.1073J. doi:10.1126/science.1242005. PMID 24288327.
  3. ^ Aruoja, Villem; Sihtmäe, Mariliis; Dubourguier, Henri-Charles; Kahru, Anne (2011). "Toxicity of 58 substituted anilines and phenols to algae Pseudokirchneriella subcapitata and bacteria Vibrio fischeri: Comparison with published data and QSARs". Chemosphere. 84 (10): 1310–1320. Bibcode:2011Chmsp..84.1310A. doi:10.1016/j.chemosphere.2011.05.023. PMID 21664645.
  4. ^ Suchana, Shamsunnahar; Araujo, Sofia Pimentel; Lomheim, Line; Mack, E. Erin; Spain, Jim C.; Edwards, Elizabeth; Passeport, Elodie (2024). "Compound-Specific Carbon, Nitrogen, and Hydrogen Isotope Analysis to Characterize Aerobic Biodegradation of 2,3-Dichloroaniline by a Mixed Enrichment Culture". Environmental Science & Technology. 58 (27): 12042–12050. Bibcode:2024EnST...5812042S. doi:10.1021/acs.est.4c02173. PMID 38934904.