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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

GLP study reporting acute oral LD50 in fasted rats > 5000 mg/kg (OECD 401)
GLP study reporting acute dermal LD50 in rats > 2000 mg/kg (OECD 402)

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
LD50
Value:
5 000 mg/kg bw

Acute toxicity: via dermal route

Endpoint conclusion
Dose descriptor:
LD50
Value:
2 000 mg/kg bw

Additional information

Recovery from oral exposure, as judged by external appearance and behaviour, was advanced by Day 3 and complete by Day 4. Similarly, animals exposed to the test substance via the dermal route had recovered by Day 4. Exposure via inhalation is not considered to be of importance because the substance is non-volatile in the solid form and as the commercially available liquid form in carrier oil.

Justification for classification or non-classification

The test substance does not meet the criteria for classification as acutely toxic under the terms of Directive 67/548/EEC or GHS as reflected by Regulation (EC) 1272/2008.