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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

The studies on acute oral toxicity were not performed according to guideline methods. However, the number of treated animals and the used protocols are scientifically acceptable to evaluate this endpoint sufficiently. 
A valid study on acute inhalation toxicity according OECD TG 403 was conducted

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
LD50
Value:
3 180 mg/kg bw

Acute toxicity: via inhalation route

Endpoint conclusion
Dose descriptor:
LC50
Value:
5 289 mg/m³ air

Additional information

Studies on rats and mice showed acute oral toxicity with LD50 values higher than 2000 mg/kg bw with one exception were a value of 940 mg/kg bw was found in an insufficient documented mutagenic evaluation study.

In the acute inhalation toxicity study on rats a LC50 (aerosol, 4h) = 5289 mg/m³ was determined.

In a study from a secondary source a LD50 > 5000 mg/kg bw was ffound for acute dermal toxicity.

Justification for classification or non-classification

The acute oral toxicity studies demonstrated a low systemic toxicity with LD50 values higher than 2000 mg/kg bw.

In the acute inhalation study a LC50 > 5000 mg/m³ was (rat, aerosol, 4 h) was determined.

A classification is therefore noit justified.