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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Endpoint summary

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Administrative data

Key value for chemical safety assessment

Genetic toxicity in vitro

Description of key information
  • Negative Ames test (OECD 471)
  • Negative in vitro bacterial DNA damage / repair assay
  • Negative in vitro micronucleus assay
Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (negative)

Genetic toxicity in vivo

Description of key information
  • Negative in vivo mouse micronucleus test (OECD 487)
Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (negative)

Additional information

Justification for classification or non-classification

The results of in vitro gene mutation studies of TPP in bacteria, a bacterial DNA damage / repair assay, an in vitro human lymphocyte micronucleus assay, and an in vivo mouse micronucleus test were all negative. Therefore, it is concluded that TPP is not genotoxic and does not warrant classification for mutagenicity according to CLP Regulation EC 1272/2008.