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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Oral (OECD 423), rat: LD50 cut-off = 2000 mg/kg bw

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
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

The acute oral toxicity of the test substance was assessed in a study according to OECD Guideline 423 and in compliance with GLP (2016). In step 1, the test substance was administered via oral gavage to 3 female rats at dose level of 2000 mg/kg bw. Since no mortality occurred, 2000 mg/kg bw was administered to 3 further animals in a second step. One animal was found dead each on Day 2 and 3 after administration. Therefore, 300 mg/kg bw was administered to 3 animals each in step 3 and 4. No mortality was observed at 300 mg/kg bw. Based on the results a LD50 cut-off of 2000 mg/kg bw was determined in this study.

Justification for classification or non-classification

The available data on acute oral toxicity of the test substance meet the criteria for Acute Tox. Cat 4 (H302) according to Regulation (EC) No 1272/2008.