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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

Oral rat fixed dose: LD50 > 2000 mg/kg bw

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
LD50
Value:
2 000 mg/kg bw

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

A high reliable study according to OECD guideline 420 was performed with 5 female Wistar rats under GLP conditions. The animals were treated with 2000 mg/kg bw of the test substance by gavage in a single dose. Clinical signs like ataxia, hunched posture, lethargy and ptosis were observed. The animals appeared normal for four hours or one day after dosing and no deaths occured. The LD50 was therefore set to be > 2000 mg/kg bw.

Justification for classification or non-classification

No mortalities occured in a fixed dose study at 2000 mg/kg bw, therefore the test substance was not classified according to DSD and CLP.