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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Effects on fertility

Effect on fertility: via oral route
Dose descriptor:
NOAEL
1 000 mg/kg bw/day
Additional information

The test substance did not induce any toxic effects in parent males and females, did not disturb their capacity of reproduction and did not impair the development of the F1 offspring. Under the conditions, the highest tested dose of 1000 mg/kg bw/day was found to be the NOEL. According to Directive 67/548/EEC, no classification is warranted. According to Regulation (EC) No. 1272/2008, no classification is warranted.


Short description of key information:
A one generation study by oral route (gavage) was carried out in rats according to OECD test guideline 415.

Effects on developmental toxicity

Description of key information
An embryotoxicity/teratogenicity study by oral route was carried out in rats according to OECD guideline 414.
Effect on developmental toxicity: via oral route
Dose descriptor:
NOAEL
1 000 mg/kg bw/day
Additional information

The test substance was well tolerated by the dams at all the dose levels and was neither embryonic or teratogenic. The No Observable Adverse Effect Level is defined as 1000 mg/kg bw/day in terms of maternotoxic effects and embryofetal development.The No Observable Effect Level is defined as 1000 mg/kg bw/day in terms of maternotoxic effects and embryofetal development.

Justification for classification or non-classification

According to Directive 67/548/EEC, no classification is warranted. According to Regulation (EC) No. 1272/2008, no classification is warranted.

Additional information