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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

No mortality in an acute oral limit dose test (OECD guideline 423- acute toxic class method). LD50 > 2000 mg/kg bw. 

Key value for chemical safety assessment

Additional information

Acute oral:

In an acute oral limit dose test (OECD guideline 423- acute toxic class method) in Wistar rats, no mortality was observed following the gavage of 2000 mg/kg bw (BASF AG, 1998). Furthermore no clinical signs were observed in males and in females apart of reversible impaired general state, dyspnoea, staggering and piloerection.

 

Inhalation:

No valid acute inhalation assay with an enriched and characterized aerosol exposure is available. Though the available inhalation risk assays with atmospheres saturated with vapors of the volatile components of a test substance did not identify mortality or signs of systemic toxicity in rats (BASF AG, 1962/1963).

 

Dermal:

No valid acute dermal assay is available. In a rather uncommon assay shaved rats were placed with their bellies for 4 hours in a tub filled with 10-15 g of the undiluted test substance (BASF AG, 1998). No mortalities and no symptoms of systemic toxicity were observed. Although no conclusions on dose etc. can be made.

Justification for classification or non-classification

No classification since no mortality was observed in an acute oral limit dose test (OECD guideline 423- acute toxic class method) at a dose level of 2000 mg/kg bw.