# Re‐evaluation of sucralose (E 955) as a food additive and evaluation of a new application on extension of use of sucralose (E 955) in fine bakery wares

**Authors:** Laurence Castle, Monica Andreassen, Gabriele Aquilina, Maria Lourdes Bastos, Polly Boon, Biagio Fallico, Reginald FitzGerald, Maria Jose Frutos Fernandez, Bettina Grasl‐Kraupp, Ursula Gundert‐Remy, Rainer Gürtler, Eric Houdeau, Marcin Kurek, Henriqueta Louro, Patricia Morales, Sabina Passamonti, Monika Batke, Antonios Dourus, James Chipman, Riccardo Crebelli, Peter Fürst, Thorhallur Halldorsson, Manuela Mirat, Alicja Mortensen, Matthew Wright, Oliver Lindtner, Stefania Barmaz, Consuelo Civitella, Zsuzsanna Horvath, Sara Levorato, Elena Mazzoli, Josef Daniel Rasinger, Ana Maria Rincon, Camilla Smeraldi, Alexandra Tard, Federica Lodi

PMC · DOI: 10.2903/j.efsa.2026.9854 · EFSA Journal · 2026-02-17

## TL;DR

This paper re-evaluates the safety of the food additive sucralose and considers its proposed use in fine bakery products, finding no major safety concerns but uncertainty about its extended use.

## Contribution

The paper provides a re-evaluation of sucralose safety and assesses a new application in fine bakery wares using updated toxicological data.

## Key findings

- No safety concerns were identified for genotoxicity of sucralose and its impurities.
- The current acceptable daily intake (ADI) of 15 mg/kg bw per day remains valid.
- The proposed extension of use in fine bakery wares could not be confirmed as safe due to uncertainties about chlorinated compound formation.

## Abstract

The present opinion deals with the re‐evaluation of sucralose (E 955) as food additive and with the safety of a proposed extension of use in food category (FC) 7.2 ‘Fine bakery wares’. Based on the available data, no safety concerns arose for genotoxicity of sucralose (E 955) and its impurities and degradation products. Based on the weight of evidence (WoE), the Panel considered the decrease in body weight observed in rats as the relevant endpoint for the derivation of a reference point (RP). The Panel performed a benchmark dose (BMD) analysis on the data from the longest study (combined chronic and carcinogenicity study) with a modified benchmark dose response to account for the poor palatability of sucralose. The resulting RP was 55 mg/kg bw per day (benchmark dose lower confidence limit; BMDL). The Panel considered it appropriate to derive chemical‐specific assessment factor for sucralose and concluded that there is no need to revise the current ADI of 15 mg/kg bw per day of sucralose (E 955) previously established by the Scientific Committee on Food. The exposure estimates considering the currently authorised uses did not exceed the ADI. Therefore, the Panel concluded that there is no safety concern at the reported uses and use levels of sucralose (E 955). The overall exposure did not increase substantially when considering the proposed extension of use. However, based on the available data and the identified uncertainties regarding the potential formation of chlorinated compounds under the wide range of baking processes that may be applicable for FC 7.2, the Panel could not conclude on the safety of the proposed extension of use of E 955 in this FC. The Panel issued recommendations to the European Commission, primarily to consider a revision of the EU specifications for sucralose.

## Linked entities

- **Chemicals:** sucralose (PubChem CID 71485)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Diseases:** carcinogenicity (MESH:D011230)
- **Chemicals:** E 955 (MESH:C026285)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

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## References

303 references — full list in the complete paper: https://tomesphere.com/paper/PMC12911467/full.md

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Source: https://tomesphere.com/paper/PMC12911467