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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

There is no study available with the target substance. In a study similar to OECD TG 423 performed with the structural analogue substance Iron cobalt chromite black spinel a discriminating dose > 2000 mg/kg bw in rats was observed.

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
discriminating dose
Value:
2 000 mg/kg bw
Quality of whole database:
similar to OECD TG 423 (Read Across)

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Oral

In an acute oral toxicity study similar to OECD TG 423, Sprague Dawley rats (3 males + 3 females) were given a single oral dose of the structural analogue substance Iron cobalt chromite black spinel (2000 mg/kg bw). Animals were observed for 14 days and necropsy was performed. All animals survived until the end of the observation period. Neither abnormal effects nor any toxicity signs that could be attributed to the test item were observed. The body weight gain of the treated animals was similar to that of control animals. At necropsy no substance-related signs of toxicity were detected. The discriminating dose was > 2000 mg/kg bw ( Laboratorio de análisis Dr. Echevarne-Laboratorio, 2003).

 

Justification for classification or non-classification

Classification, Labelling, and Packaging Regulation (EC) No 1272/2008

The available experimental test data is reliable and suitable for classification purposes under Regulation (EC) No 1272/2008. As a result the substance is not considered to be classified for acute toxicity under Regulation (EC) No 1272/2008, as amended for the tenth time in Regulation (EU) No 2017/776.