Facile synthesis of oligo anilines as permanent hair dyes: How chemical modifications impart colour and avoid toxicity

Gopalakrishnan Venkatesan, Yuri Dancik, Arup Sinha, Mei Bigliardi, Ramasamy Srinivas, Thomas Dawson, Suresh Valiyaveettil, Paul Bigliardi, Giorgia Pastorin

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Many dyes for long-lasting hair coloring contain aromatic amines that undergo oxidative polymerizations, resulting in allergic contact dermatitis, with the potential to develop serious toxic effects. Among these amines, para-phenylenediamine (PPD) is a small molecule form of aniline commonly used in beauty products despite being a known allergen to humans. Hence, in this study we designed and synthesized safer PPD analogues through the synthesis of oligomeric PPD and the introduction of bulky side chains on PPD to overcome the PPD dye's toxicity. We hypothesized that (a) an increase in the molecular size of PPD by addition of the PPD monomer unit on free amines and (b) strategic functionalizations at the ortho position of PPD with strong electron-donating bulky groups are able to maintain the hair coloring properties, and increase the resistance to binding to skin proteins and therefore decrease the chance of skin sensitization. 13 oligomers were synthesized, with the aim to produce safer hair dyes while minimising eventual toxicity to humans. In particular, oligomers with bulky sidechains, PPD 6 (13), PPD 7 (14) and PPD 8 (15), displayed weak-to-moderate (27.1%, 24.1% and 34.0%) sensitization potential. The results confirmed the importance of having bulky and strong electron donating O-alkyl substituents in order to decrease the reactivity of PPD analogues towards skin proteins, thus preventing the interaction with immune cells and providing safer hair dyes.

Original languageEnglish (US)
Pages (from-to)16188-16199
Number of pages12
JournalNew Journal of Chemistry
Volume43
Issue number41
DOIs
StatePublished - 2019

Bibliographical note

Funding Information:
This work was supported by the National University of Singapore (NUS, C-141-000-097-001), Department of Pharmacy (AcRF Tier 1 FRC grant R-148-000-267-114), A-STAR SERC (grant number: 152 80 00046 (R-148-000-222-305)), and R-148-000-227-720.

Publisher Copyright:
© 2019 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.

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