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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

one in vitro study on estimation of LD50 and proposed starting dose for further in vivo studies is available. one in vivo study according to OECD 423 available

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
LD50
Value:
2 500 mg/kg bw
Quality of whole database:
The available in vitro study indicates an approximate estimated LD50 of 761-1036 mg/kg body weight. As this value is within the range of 300 - 2000 mg/kg bw. The described in vitro assay is discussed in Guidance on information requirements and Chemical safety assessment, chapter R.7-a. The available in vivo study indicates an LD50 > 2000 mg/kg bw. For endpoint conclusion reported here, a dose discriptor of LD50 = 2500 mg/kg bw is chosen in accordance with OECD Guideline 423, Annex 2.

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

Justification for classification or non-classification

The available information is conclusive but not sufficient for classification.