# Overlooked Photochemical Risk of Antimicrobial Fragrances: Formation of Potent Allergens and Their Mechanistic Pathways

**Authors:** Xiaolin Niu, Junji Wu, Yi Chen, Na Luo, Yanpeng Gao

PMC · DOI: 10.3390/toxics13050386 · Toxics · 2025-05-10

## TL;DR

This study reveals that antimicrobial fragrances like cinnamaldehyde can transform into harmful allergens under UV light, posing risks to human health and the environment.

## Contribution

The study identifies new photochemical pathways and transformation products of cinnamaldehyde, highlighting their ecotoxicological and allergenic risks.

## Key findings

- Cinnamaldehyde degrades rapidly under UV light, forming five major transformation products.
- Transformation products like cinnamic acid and 1-Oxo-1H-indene cause skin and eye irritation.
- Photochemical reactions involve O2•−, 3CA*, and other reactive species, contributing to oxidation processes.

## Abstract

Antimicrobial fragrances, commonly found in household and personal care products, are frequently detected in water bodies, yet their environmental fate and transformation mechanisms remain inadequately explored. This study investigates the photochemical transformation of cinnamaldehyde (CA), a representative antimicrobial fragrance, and its consequence for toxicological effects. The results showed that under UV irradiation, 94.6% CA was eliminated within 60 min, with a degradation rate of 0.059 min−1. Laser flash photolysis, quenching experiments, and electron paramagnetic resonance spectra identified O2•− and 3CA* as the important species, contributing 29.4% and 33.6%, respectively, to the transformation process. Additionally, singlet oxygen (1O2), hydroxyl radicals (•OH), and solvated electrons (eaq−) were involved in mediating the oxidation reactions. These species facilitated photoionization and oxidation, resulting in the formation of five major transformation products, including cis-cinnamyl aldehyde, cinnamic acid, styrene, 1aH-indeno [1,2-b]oxirene), and 1-Oxo-1H-indene. Most of these products were persistent, and exhibited considerable ecotoxicological risks. Specifically, the cinnamic acid and 1-Oxo-1H-indene caused severe skin irritation, while cinnamic acid induced significant eye irritation. Notably, the transformation products demonstrated sensitizing effects on human skin. This study underscores the overlooked ecotoxicological risks associated with the photochemical transformation of antimicrobial fragrances, revealing their potential to generate potent allergens and other harmful byproducts.

## Linked entities

- **Chemicals:** cinnamaldehyde (PubChem CID 637511), O2•− (PubChem CID 977), 3CA* (PubChem CID 5287495), singlet oxygen (PubChem CID 159832), cinnamic acid (PubChem CID 444539), styrene (PubChem CID 7501), 1aH-indeno [1,2-b]oxirene (PubChem CID 6453553)

## Full-text entities

- **Diseases:** skin irritation (MESH:D012871), eye irritation (MESH:D005128)
- **Chemicals:** cinnamaldehyde (MESH:C012843), styrene (MESH:D020058), OH (MESH:C031356), CA (MESH:D002118), O (MESH:D010100), 1-Oxo-1H-indene (-), hydroxyl radicals (MESH:D017665), singlet oxygen (MESH:D026082), cinnamic acid (MESH:C029010)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12115848/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12115848/full.md

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Source: https://tomesphere.com/paper/PMC12115848