# Methyl N-methylanthranilate

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**Safety rating:** UNKNOWN
**CAS number:** 85-91-6
**Category:** flavoring
**FDA GRAS:** no
**Adverse events (FDA AERS):** 0
**FDA recalls:** 0
**Last updated:** 2026-04-02

## Summary

Methyl N-methylanthranilate (CAS 85-91-6) is an organic compound used as a flavoring agent and flavor enhancer in food products. It is not on the FDA's GRAS (Generally Recognized as Safe) list and has limited regulatory approval in most jurisdictions.

## Regulatory status

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

## Detailed analysis

## What is Methyl N-methylanthranilate?

Methyl N-methylanthranilate is a synthetic organic compound belonging to the anthranilate family of chemicals. It is characterized by a methyl-substituted anthranilic acid ester structure. The compound is used primarily in the food industry as a flavoring agent, often employed to create or enhance fruity flavor profiles in various food and beverage products.

## Common Uses

Methyl N-methylanthranilate is utilized in flavoring applications, particularly in products where fruity or grape-like taste notes are desired. It may be incorporated into beverages, confectionery, desserts, and other processed foods as part of proprietary flavoring blends. The compound is typically used in very small quantities, measured in parts per million, consistent with standard flavoring agent applications. Its use varies significantly by country based on individual regulatory frameworks governing food additives.

## Safety Assessment

As of the available data, there have been zero adverse events reported to the FDA related to this additive, and no food recalls have been attributed to it. However, it is important to note that the absence of reported adverse events does not constitute an approval determination. The compound has not been subjected to the formal FDA GRAS (Generally Recognized as Safe) review process, which means it has not received the comprehensive safety assessment that many other flavoring agents have undergone.

Toxicological data on this specific compound appears limited in the public domain. Safety information for structurally related anthranilate compounds suggests generally low acute toxicity profiles, but specific and comprehensive safety studies for methyl N-methylanthranilate would be necessary to establish definitive safety parameters. The limited regulatory approval status reflects either the relatively recent development of safety data, limited industry petition for approval, or insufficient toxicological evidence to warrant GRAS designation.

## Regulatory Status

Methyl N-methylanthranilate does not appear on the FDA's GRAS list, which means it cannot be used in food products intended for the U.S. market under the Generally Recognized as Safe exemption. Its regulatory status in other jurisdictions varies; it may be approved in some countries' flavoring ingredient lists while remaining restricted or unapproved in others. The European Union maintains separate approval processes for food flavoring agents under Regulation (EC) No 1334/2008, and this compound's status within that framework would require verification against current EU flavoring regulations.

Manufacturers seeking to use this additive must typically comply with specific regional regulations and may require individual approval or notification before market introduction. The lack of GRAS status in the United States represents a significant regulatory barrier to its use in American food products.

## Key Studies

Published scientific literature specifically addressing the safety profile of methyl N-methylanthranilate appears limited in the readily available peer-reviewed domain. Most safety assessments for this compound would derive from proprietary toxicological studies submitted during regulatory review processes in jurisdictions where approval has been sought. General knowledge regarding anthranilate-class compounds suggests metabolic pathways and toxicity patterns are relatively well-understood within this chemical family, but substance-specific data would be essential for comprehensive risk assessment.

Any manufacturer or regulatory agency reviewing this compound would require access to complete toxicological dossiers, including acute toxicity studies, subchronic and chronic exposure studies, genotoxicity assessments, and reproductive toxicity data before determining appropriate safety conclusions.

## 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. "Methyl N-methylanthranilate — Safety, regulation, and evidence." https://additivefacts.com/additives/methyl-n-methylanthranilate. Accessed 2026-05-19.
