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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
LD50
Value:
200 mg/kg bw

Acute toxicity: via inhalation route

Endpoint conclusion
Value:
mg/m³ air

Acute toxicity: via dermal route

Endpoint conclusion
Dose descriptor:
LD50
Value:
200 mg/kg bw

Additional information

The LD50following dermal application to rabbits ranged between 200 and 316 mg/kg bw and LD50(oral,rat) was 200 mg/kg bw.

Justification for classification or non-classification

Oral:

The oral LD50 in the rats is 200 mg/kg bw (Bayer, 1978) and 240 mg/kg bw (Younger Laboratories Inc., 1977).

Based on the test results and according to the EC criteria for classification and labelling requirements for dangerous substances and mixtures the test substance is classified asAcute Tox. 3 H301 Toxic if swallowed according to Regulation (EC) No 1272/2008 criteria (T; R25 Toxic if swallowed according to DSD criteria).

Dermal:

The LD50 following dermal application to rabbits ranges between 200 and 316 mg/kg bw (Younger Laboratories Inc., 1977).

Based on the test results and according to the EC criteria for classification and labelling requirements for dangerous substances and mixtures the test substance is classified asAcute Tox. 3 H311 Toxic in contact with skinaccording to Regulation (EC) No 1272/2008 criteria (T; R24 Toxic in contact with skin according to DSD criteria).

Inhalation:

Not classified. The LC50 was not determined in any of two inhalation studies (Younger Laboratories Inc. , 1977;BASF AG: Zeller H, Oettel H, 1965)