Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Key value for chemical safety assessment

Additional information

No effects have been reported in a suitable test battery including in-vitro genotoxicity/cytogenicity test in bacteria and mammalian cells, and an in vivo test conducted with closely related structural analogues. Details on the read-across justification are summarized in the attached read-across report.


Justification for selection of genetic toxicity endpoint
GLP guideline study

Short description of key information:
HPRT assay (GLP, OECD 476, Harlan, 2012) on Glycerides, C16-18 mono-, di and tri-, hydrogenated, citrates, potassium salts; Ames Test (GLP, OECD 476, Huels, 1996) on a structural similar substance;
In addition Hayes et al. 1994 reported negative results in a set of three mutagenicity tests (HPRT (similar to OECD 476), Chromosome aberration (similar to OECD 473), and in vivo micronucleus assay (similar to OECD 474), using SALATRIM (Short and long chain acyl triglyceride molecule).

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

No effects have been reported in a suitable test battery including in-vitro genotoxicity/cytogenicity test in bacteria and mammalian cells, and an in vivo test conducted with closely related structural analogues.