4-Chlorophenylamine

CAS : 106-47-8

Ref. 3D-FC20361

Informations sur le produit

• Nom: 4-Chlorophenylamine
• Synonymes: p-Aminochlorobenzenep-Chloroaniline4-Chloro-1-aminobenzene, 1-Amino-4-Chlorobenzene, 4-Amino-1-chlorobenzene, 4-Aminochlorobenzene, 4-Chloranilin, 4-Chloro-1-aminobenzene, 4-Chloroanilinium Chloride, 4-Chloroanline, 4-Chlorobenzenamine, 4-Chlorobenzeneamine, 4-Chlorophenyamine, 4-Choraniline, 4-Cloroanilina, Aniline, 4-Chloro-, Aniline, p-chloro-, Benzenamine, 4-chloro-, Boron Fluoride 4-Chloroaniline (1:3:1), Chloroaminobenzene, p-, Chloroaniline, 4-, Chloroaniline, p-, N-chloroaniline, Nsc 36941, P-Aminochlorobenzene, Parachloroaniline, Pestanal, p-Chloroaniline, p-Chlorophenylamine

Description

4-Chlorophenylamine is a toxic chemical that belongs to the group of aromatic amines. It has been used in the production of dyes, pesticides, and pharmaceuticals. The acute toxicity of 4-chloroaniline was studied using locomotor activity tests with male and female rats. The plasma mass spectrometry showed that 4-chloroaniline is metabolized to form 4-aminophenol, 4-aminoacetanilide, and 2,4-diaminophenol. Acute toxicity studies show that potassium dichromate has a low toxicity for humans as it is rapidly excreted through urine. Long-term toxicity studies have shown that hydrogen tartrate can cause renal necrosis in rats after repeated administration. The reaction mechanism of hydrogen tartrate is an addition reaction with the hydroxyl group on the benzene ring in 4-chloroaniline to produce water and nitrite ion. Carcinogenic potential was assessed by measuring

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 127.57 g/mol
• Formule: C₆H₆ClN
• Degré de pureté: Min. 95%
• Couleur/Forme: White Powder
• InChI: InChI=1S/C6H6ClN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2
• Code InChI: InChIKey=QSNSCYSYFYORTR-UHFFFAOYSA-N
• SMILES: Nc1ccc(Cl)cc1