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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Data on acute oral toxicity are not available (study technically not feasable; low boiling point).
In acute inhalation studies in rats the LC50 (4h) was > 20165 ppm (48 mg/L).
The LD50 in acute dermal toxicity studies with cold liquid in rabbits was >5000 mg/kg bw.

Key value for chemical safety assessment

Additional information

Oral

Data on acute oral toxicity are not available (study technically not feasable; low boiling point).

Inhalation

No mortality and no clinical signs were found in 10 male and 10 female rats within 14 days after exposure for 4 h to the dose level of 5.3 mg/L (BASF 1980). Also at a dose level of 20165 ppm (48 mg/L) no mortality and no clinical signs were detected in rats exposed for 4 h (post exposure period 14 days (Dow 1990)). In both studies no macroscopic findings were seen at necropsy.

Dermal

No systemic clinical signs and no mortality were reported after 24 h occlusive exposure to 8 mL/kg bw (ca. 5000 mg/kg bw; cold liquid) in two New Zealand White rabbits; the acute dermal LD50 is considered to be > 5000 mg/kg bw (Dow 1990).

Justification for classification or non-classification

Classification for acute toxicity is not warranted according to the criteria of EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008.