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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 (rat): LD50 > 5000 mg/kg bw (m+f)

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
LD50
Value:
5 000 mg/kg bw

Additional information

The test material was tested for acute toxicity via oralapplication to rats.An LD50 of > 5000 mg/kg was identified.No mortality occurred. No signs of systemic toxicity, or behavioral changes were reported during the study, and no abnormalities were noted at necropsy, except one female rat showed mild hydrometra in uterus. All animals showed expected bodyweight gain during the study except female group during day 7 to day 14 period.

Justification for classification or non-classification

There are conclusive but not sufficient data for classification of the test item with regard to acute toxicity. The substance is not classified for acute toxicity via oral route in accordance to Directive 67/548/EEC or the CLP Regulation (EC) No 1272/2008.