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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

There is no experimental data available on gene mutation in bacteria for the substance dipraseodymium dizirconium heptaoxide. However, based on a weight of evidence approach including results of Ames tests performed with the constituents of the substance, i.e. praseodymium(III,IV) oxide and zirconium dioxide, it can be concluded that the substance is not expected to be mutagenic in bacteria either.

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

Genetic toxicity in vivo

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

1. Information on praseodymium(III,IV) oxide

Mutagenic potential of praseodymium(III,IV) oxide was evaluated using an Ames test performed according to OECD guideline 471 and in compliance with GLP. Five strains of Salmonella typhimurium (TA 1535, TA 1537, TA98, TA 100 and TA 102) were used in this study and exposed to a concentration series of the test item in the presence and absence of metabolic activation (Haddouk, 2007; Klimisch 1). Under the conditions of this study, praseodymium(III,IV) oxide did not show any mutagenic activity in the Salmonella strains tested, both in the absence and presence of metabolic activation.

2. Information on zirconium dioxide

A similar GLP-compliant OECD 471 study is available for zirconium dioxide. Five strains of Salmonella typhimurium (TA 97a, TA 98, TA 100, TA 102, TA 1535) were tested in the presence and absence of metabolic activation (LAUS GmbH, 2008; Klimisch 1). Under the conditions of this study, zirconium dioxide was not found to be mutagenic in the absence and presence of metabolic activation in the Salmonella strains tested.

3. Conclusion on the substance dipraseodymium dizirconium heptaoxide:

Based on the negative results obtained for its constituents praseodymium(III,IV) oxide and zirconium dioxide, the substance can safely be concluded not to be mutagenic to bacteria either.

Justification for classification or non-classification

Based on the negative results obtained for its constituents, the substance dipraseodymium dizirconium heptaoxide can safely be concluded not to be mutagenic to bacteria either.

Neither praseodymium(III,IV) oxide nor zirconium dioxide is classified for genetic toxicity. Therefore, the reaction mass of these two oxides is not classified for genetic toxicity either.