# Repeatable Perming via Thiol–Michael Click Reaction: Using Amide Derived from Maleic Acid and Cystine

**Authors:** Zezhi Liu, Ling Ma, Timson Chen, Zhizhen Li, Ya Chen, Jinhua Li, Kuan Chang, Jing Wang

PMC · DOI: 10.3390/molecules31020382 · 2026-01-21

## TL;DR

A new perming method using a thiol–Michael click reaction avoids hair damage and allows repeat use without oxidative agents.

## Contribution

A novel thiol–Michael click perming molecule, MA2-CySS, enables repeatable perming with minimal damage.

## Key findings

- MA2-CySS perming showed no cytotoxicity and reached reaction plateau within 30 minutes.
- MA2-CySS perming reduced color change and cuticle damage while maintaining hair strength across three cycles.
- Raman spectroscopy showed MA2-CySS preserved hair keratin structure better than oxidative perming.

## Abstract

Conventional perming relies on oxidative agents that significantly damage hair. The thiol–Michael click perming strategy derived from linear aliphatic diols and diamines has been developed to avoid oxidative damage, but lacks repeatable perming capabilities. In this study, a novel thiol–Michael click perming molecule was proposed for repeatable perming while avoiding oxidative damage. N,N′-bis(maleoyl)-l-cystine (MA2-CySS) was synthesized and characterized through Raman spectroscopy and 1H NMR with MTT assay demonstrated no cytotoxicity up to 1000 μg/mL. Click reactivity analysis revealed that the reaction reached a plateau after 30 min, with alkaline pH and elevated temperatures significantly enhancing reactivity. MA2-CySS perming achieved efficiency comparable to oxidative perming, exceeding 1300% across three perming cycles. MA2-CySS perming significantly reduced both color change and cuticle damage, as demonstrated by color difference measurements and SEM, while maintaining superior mechanical properties as revealed by tensile property tests. Raman spectroscopy demonstrated that MA2-CySS perming better preserves hair keratin’s secondary structure, maintaining superior α-helix content at 27.50% versus 24.35%, exhibiting higher disulfide bond retention at 85% versus 72%, and showing gauche–gauche–gauche to trans–gauche–trans conformational conversion at 9% versus 6%. This study demonstrates that repeatable perming via thiol–Michael click reaction represents a significant advancement in perming methodology.

## Linked entities

- **Chemicals:** maleic acid (PubChem CID 444266), cystine (PubChem CID 67678)

## Full-text entities

- **Diseases:** cytotoxicity (MESH:D064420)
- **Chemicals:** 1H (-), Thiol (MESH:D013438), Maleic Acid (MESH:C030272), diols (MESH:D011276), diamines (MESH:D003959), MTT (MESH:C070243), Cystine (MESH:D003553), disulfide (MESH:D004220)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12844010/full.md

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Source: https://tomesphere.com/paper/PMC12844010