Registration Dossier

Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

In the rat reproduction toxicity study, DBU was administered for 29 days to male rats and for 43 to 57 days to female rats. Doses of 150 mg / kg body weight have caused the appearance of parental toxicity, with macroscopic effects such as dark red stools and irregular stomach surface. Microscopic analysis showed hemorrhage, degeneration of the glandular mucosa, inflammation, hyperplasia, and hyperkeratosis. All effects were local and limited to the stomach, and can be attributed to the strong alkaline corrosiveness of the DBU. No other toxicologically significant change was observed in animals treated with 150 mg / kg body weight of DBU, whereas no adverse effects were found for the remaining dosages. The NOAEL for parental toxicity was then set at 50 mg / kg of body weight.

Key value for chemical safety assessment

Additional information

Bibliographic source:

REACH Registration Dossier, 1,8-diazabicyclo[5.4.0]undec-7-ene

Justification for classification or non-classification

All effects were local and limited to the stomach, and can be attributed to the strong alkaline corrosiveness of the DBU. No other toxicologically significant change was observed in the treated animals.

No classification is proposed based on available data.