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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
acute toxicity: oral
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
other:
Justification for type of information:
An acute intravenous toxicity study is available and shows an LD50 of 45.2 mg / kg.
If we consider this same value for exposure by ingestion, our approach is greater since we consider that 100% of the substance ingested is found in the blood system (which is not the case since the average oral bioavailability is less than 50%).
Considering an LD50 of 45.2 mg / kg, the risk of ingestion is overestimated.
With a such result, the subtsnace is considered as toxic by oral route - Cat. 2.

Data source

Materials and methods

Results and discussion

Applicant's summary and conclusion