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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Genetic toxicity in vitro

Description of key information

Bacterial Gene Mutation (Ames Test)

In a reliable OECD Guideline 471 GLP study, TiTDP was not mutagenic to any of 5 strains of S. typhimurium when tested in the absence and presence of an exogenous metabolic activation system (rat liver S9) at concentrations up to those producing cytoxicity.

Mammalian Gene Mutation

No effects in a new OECD Guideline 476 study on TiTDP.

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (negative)

Genetic toxicity in vivo

Description of key information

Chromosomal Aberration (Mouse Micronucleus)

In a reliable OECD 474 Guideline GLP study (Gaikwad, 2014), TiTDP did not cause micronucleus induction in male and female mice when administered at a limit dose of 2000 mg/kg bw by gavage for two consecutive days.

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (negative)

Additional information

All available genetic toxicity study results are negative on closely related analogs. Test results are available for TiTDP in in vitro bacterial and mammalian agene mutation and in vivo chromosome aberration studies and also for TDP.

Justification for classification or non-classification

All available genetic toxicity study results are negative. Therefore, it is concluded that TiTDP is not genotoxic and does not warrant classification for mutagenicity.