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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

LD50 (oral) = 84.18 mg/kg bw

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
adverse effect observed
Dose descriptor:
LD50
Value:
84.18 mg/kg bw

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

To evaluate Acute toxicity of the test item the In vitro NRU cytotoxicity assay on Balb/3T3 cells was used.

Justification for classification or non-classification

According to the CLP Regulation (EC n. 1272/2008), Part 3: Health Hazards, the substances can be classified for acute toxicity when the following criteria are met:

Category 1: 0 < LD50 <= 5

Category 2: 5 < LD50 <= 50

Category 3: 50 < LD50 <= 300

Category 4: 300 < LD50 <= 2000

Based on the available data the LD50 is estimated to be equal to 84.18 mg/kg bw.Therefore, the classification for acute toxicity is Category 3 according to the CLP Regulation (EC 1272/2008).