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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Oral:
LD50 (Wistar rat) > 2000 mg/kg bw (OECD TG 423, GLP compliant) (Testing Lab.: RCC Ltd., 2005; Study Owner: BASF SE)
Dermal:
LD50 (Wistar rat) > 2000 mg/kg bw (OECD TG 402, GLP compliant) (Testing Lab.: RCC Ltd., 2005; Study Owner: BASF SE)
Inhalation:
no data available

Key value for chemical safety assessment

Acute toxicity: via oral route

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

Acute toxicity: via dermal route

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

Additional information

At a single dose of 2000 mg/kg bw, no mortality occurred and no clinical findings were observed after test article administration via the oral and dermal route, respectively. No information on acute inhalative toxicity is available.

Justification for classification or non-classification

There are conclusive data that classification of the test item with regard to acute toxicity is not necessary.

The test item is not classified for this endpoint in accordance with Directive 67/548/EEC or with the CLP Regulation (EC) No 1272/2008 reflecting GHS regulations.