# Resorcinol

> Source URL: https://additivefacts.com/additives/resorcinol
> Markdown URL: https://additivefacts.com/additives/resorcinol.md

**Safety rating:** CAUTION
**CAS number:** 108-46-3
**Category:** flavoring
**FDA GRAS:** no
**Adverse events (FDA AERS):** 0
**FDA recalls:** 0
**Last updated:** 2026-04-04

## Summary

Resorcinol (1,3-benzenediol) is an organic compound used as a flavoring agent and flavor enhancer in food products. While not currently approved as GRAS by the FDA, it has not been associated with reported adverse events or recalls in food applications.

## Regulatory status

| Country | Status |
| --- | --- |
| United States | approved |
| European Union | not_evaluated |
| United Kingdom | approved |
| Canada | approved |
| Australia | approved |
| Japan | approved |
| South Korea | approved |
| Brazil | approved |
| China | approved |
| India | approved |

## Detailed analysis

## What is Resorcinol?

Resorcinol, chemically known as 1,3-benzenediol or m-dihydroxybenzene (CAS Number 108-46-3), is a white crystalline organic compound derived from benzene. It belongs to the class of dihydric phenols and has been used in various industrial and personal care applications for over a century. In the food industry, resorcinol is classified as a flavoring agent and flavor enhancer, though its use in food is limited and regulated differently across jurisdictions.

## Common Uses

Resorcinol's primary applications in food are as a flavoring agent and flavor enhancer, where it may contribute to specific taste profiles in processed foods and beverages. However, its food use is significantly restricted compared to other flavor enhancers. The compound has broader applications outside of food, including use in pharmaceutical formulations, cosmetics, and industrial processes. In food manufacturing, when used, it typically appears in very small quantities as part of complex flavoring systems.

## Safety Assessment

According to FDA records, there have been zero reported adverse events and zero recalls associated with resorcinol in food applications. This absence of reported incidents suggests that if resorcinol is present in food products, it has not generated consumer safety concerns significant enough to trigger regulatory action or public health alerts.

Resorcinol has been studied for various health effects in non-food contexts. Dermal and oral toxicity studies in animals have been conducted, primarily due to its use in other industries. The compound is known to penetrate skin and has been evaluated for systemic effects. However, the concentration levels and exposure routes in food use differ substantially from other applications.

## Regulatory Status

Resorcinol has not received GRAS (Generally Recognized As Safe) approval from the FDA for food use. This designation is significant—while it does not necessarily indicate the substance is unsafe, it means that resorcinol has not been formally determined to be safe for intentional food addition under the conditions of its intended use in the United States.

The regulatory status varies internationally. Different countries maintain separate approval lists for food additives, and resorcinol's status in the European Union, Japan, and other regions may differ from FDA determinations. The European Food Safety Authority (EFSA) maintains its own evaluations of food additives, which may classify resorcinol differently.

Within the United States, food manufacturers seeking to use resorcinol would need to follow specific regulatory pathways, which may include food additive petitions or other compliance mechanisms, depending on the specific application and concentration levels.

## Key Studies

Toxicological research on resorcinol has primarily focused on its use in non-food applications such as pharmaceuticals and cosmetics. These studies have examined dermal penetration, systemic absorption, and potential effects on various organ systems. However, specific safety studies focused on food-level exposure to resorcinol are limited in the published scientific literature.

The absence of formal GRAS status suggests that comprehensive safety data packages specifically documenting food-use safety—including the levels of use, food categories, and consumer exposure scenarios—have not been submitted to or approved by the FDA. Such packages would typically include chemistry data, toxicology studies, and exposure assessment information.

Researchers and regulatory agencies continue to evaluate the safety profiles of flavoring compounds, and classifications may be updated as new scientific information emerges. Manufacturers and consumers should consult current regulatory guidance for the most up-to-date information regarding resorcinol in specific food products.

## Sources

- FDA Substances Added to Food (CFSAN)
- OpenFDA Adverse Event Reporting System (AERS)
- OpenFDA Food Recalls
- EFSA OpenFoodTox
- EU Food Additive Portal

## Citation

Additive Facts. "Resorcinol — Safety, regulation, and evidence." https://additivefacts.com/additives/resorcinol. Accessed 2026-05-20.