4-aminophenol

Synonyms: "4-aminophenol", "p-aminophenol", "4-hydroxyaniline", "p-hydroxyaniline", "paranol", "Certinal", "Citol", "Azol", "4-aminobenzenol", "Fouramine P", "Ursol P Base", "Rodinal", "p-Hydroxyphenylamine", "Benzofur P", "Fourrine P Base", "Pelagol P Base", "Tertral P Base", "Ursol P", "Nako Brown R", "Furro P Base", "Durafur Brown RB", "4-Amino-1-hydroxybenzene", "Renal AC", "Fourrine 84", "Phenol, p-amino-", "Zoba Brown P Base", "4-AMINO-PHENOL", "UNAL", "Pelagol Grey P Base", "BASF Ursol P Base", "C.I. Oxidation Base 6", "1-Amino-4-hydroxybenzene", "p-Aminofenol", "Para-aminophenol".

Source: 4-Aminophenol is used as a dye for textile, hair, furs and feather. It is also used as photographic developer and chemical intermediate for pharmaceutical and dyes

Identifiers:

IUPAC Name: 4-aminophenol
CAS Number: 123-30-8
PubChem ID: 403
InChiKey: PLIKAWJENQZMHA-UHFFFAOYSA-N
Canonical SMILES: C1=CC(=CC=C1N)O

Structural Properties:

Molecular Formula: C6H7NO
Molecular Weight: 109.128

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
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Burnett, C.M., Re, T.A., Rodriguez, S., Loehr, R.F. and Dressler, W.E., 1989. The toxicity of p-aminophenol in the Sprague-Dawley rat: Effects on growth, reproduction and foetal development. Food and chemical toxicology, 27(10), pp.691-698. DOI: https://doi.org/10.1016/0278-6915(89)90124-5. URL: https://www.sciencedirect.com/science/article/pii/0278691589901245.
Harada, T., Kimura, E., Hirata-Koizumi, M., Hirose, A., Kamata, E. and Ema, M., 2008. Reproductive and developmental toxicity screening study of 4-aminophenol in rats. Drug and chemical toxicology, 31(4), pp.473-486. DOI: https://doi.org/10.1080/01480540802390627. URL: https://www.tandfonline.com/doi/abs/10.1080/01480540802390627.

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