4-Aminodiphenylamine

CAS: 101-54-2

Ref. 3D-FA02149

Produktinformation

• Name: 4-Aminodiphenylamine
• Synonyme: (4-(Phenylamino)phenyl)amine, 1,4-Benzenediamine, N-phenyl-, 1,4-Benzenediamine, N1-phenyl-, 1,4-Benzenediamine, N¹-phenyl-, 1-N-Phenylbenzene-1,4-diamine, 4-(N-Phenylamino)aniline, 4-(Phenylamino)aniline, 4-Amino-Diphenylamin, 4-Amino-N-phenylaniline, 4-Aminodiphenylamin, 4-Anilinoaniline, 4-Anilinophenylamine, 4-Benzenediamine,N-phenyl-1, 4Adpa, Acna Black DF Base, Acnablackdfbase, Azoic Diazo Component 22, Azosalt R, Azosaltr, Benzenediamine, N-phenyl-, Blackbasep, Diphenyl Black, Diphenylamine, 4-Amino-, Luxan Black R, N,4'-Bianiline, N-(4-Aminophenyl)anilin, N-(4-Aminophenyl)aniline, N-(4-aminofenil)anilina, N-Phenyl-1,4-Benzenediamine, N-Phenyl-1,4-phenylenediamine, N-Phenyl-1,41phenylenediamine, N-Phenyl-P-Phenylenediamine, N-Phenyl-p-aminoaniline, N-phenylbenzene-1,4-diamine, N¹-Phenyl-1,4-benzenediamine, Nsc 3401, Nsc 37074, Peltol BR, Peltol BR II, S 789, Semidin, Semidine, Variamine Blue RT Base, Variamine Blue Rt, p-(Phenylamino)aniline, p-Aminodiphenylamine, p-Anilinoaniline, p-Phenylenediamine, N-phenyl-, p-Semidine
• CAS: 101-54-2

Beschreibung

4-Aminodiphenylamine is a chemical compound that is used as an intermediate in the production of other chemicals. It has been reported to be carcinogenic, so it should be handled with care. The reaction mechanism for this chemical compound is not well-known, but it has been shown that it reacts with hydrogen bonding interactions and can form a complex with nitrogen atoms. 4-Aminodiphenylamine has been shown to have low toxicity in animal studies, and can be synthesized using a variety of methods. This chemical compound also has biological properties that make it useful in the study of body formation and metabolism.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 184.24 g/mol
• Formel: C₁₂H₁₂N₂
• Reinheit: Min. 95%
• Farbe/Form: Powder