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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Acute oral toxicity

LD50 (male) = 395 mg/kg bw.
LD50 (female) = 275 mg/kg bw.

Acute dermal toxicity

LD0 = 2000 mg(kg

LD50 > 2000 mg/kg

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
adverse effect observed
Dose descriptor:
LD50
Value:
275 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 adverse effect observed

Additional information

Justification for classification or non-classification

According to the CLP Regulation (EC 1272/2008), table 3.1.1, acute toxicity hazard categories and acute toxicity estimates (ATE) defining the respective categories:

 

For acute toxicity by oral route:

category 1: ATE <= 5 mg/kg bw

category 2: 5 < ATE <= 50 mg/kg bw

category 3: 50 < ATE <= 300 mg/kg bw

category 4: 300 < ATE <= 2000 mg/kg bw

For acute toxicity by dermal route:

category 1: ATE <= 50 mg/kg bw

category 2: 50 < ATE <= 200 mg/kg bw

category 3: 200 < ATE <= 1000 mg/kg bw

category 4: 1000 < ATE <= 2000 mg/kg bw

Based on available information, target substance is classified as category 3 (H301) for acute oral toxicity, while it is not classified for acute dermal toxicity.