p-phenylenediamine

Synonyms: "p-phenylenediamine", "benzene-1,4-diamine", "1,4-benzenediamine", "1,4-diaminobenzene", "1,4-phenylenediamine", "4-aminoaniline", "para-phenylenediamine", "p-aminoaniline", "p-diaminobenzene", "paraphenylenediamine", "4-phenylenediamine", "p-benzenediamine", "Futramine D", "Fouramine D", "Fourrine D", "Fur Yellow", "Benzofur D", "Santoflex IC", "Santoflex LC", "Developer PF", "Tertral D", "Pelagol D", "Peltol D", "Durafur Black R", "Pelagol DR", "Pelagol Grey D", "Fourrine 1", "Furro D", "Ursol D", "Zoba Black D", "Renal PF", "Developer 13", "Nako H", "BASF ursol D", "Oxidation base 10", "Fenyle","Orsin".

Source: p-Phenylenediamine is primarily used as a dye intermediate and as a dye, including hair dye formulations

Identifiers:

IUPAC Name: benzene-1,4-diamine
CAS Number: 106-50-3
PubChem ID: 7814
InChiKey: CBCKQZAAMUWICA-UHFFFAOYSA-N
Canonical SMILES: C1=CC(=CC=C1N)N

Structural Properties:

Molecular Formula: C₆H₈N₂
Molecular Weight: 108.144

Pharmacophore Features:

Number of bond donors: 2
Number of bond acceptors: 2
Number of atoms different from hydrogen: 8

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Evidence Supporting This Chemical as an Endocrine Disruptor
TEDX List of Potential Endocrine Disruptors

Bharali, M.K. and Dutta, K., 2012. Testicular toxicity of para-phenylenediamine after subchronic topical application in rat. International journal of environmental health research, 22(3), pp.270-278. DOI: https://doi.org/10.1080/09603123.2011.634388. URL: https://www.tandfonline.com/doi/abs/10.1080/09603123.2011.634388.