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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Acute toxicity: oral: key study: The oral LD 50 was greater than 2000 mg/kg bw for rats. Test method was according to OECD guideline 401.
Acute toxicity: inhalation: key study: The LC 50 was greater than 20 mg/L for rats. Test method was according to OECD guideline 403.
Acute toxicity: dermal: Key study: The LD 50 of sodium trichloroacetate was greater than 2000 mg/kg. Test method was similar to OECD guideline 402.

Key value for chemical safety assessment

Additional information

Acute toxicity: oral:

Key study: Test method was according to OECD guideline 401. The oral LD50 was greater than 2000 mg/kg bw for rats. This result is supported by further experimental data from the company.

Acute toxicity: inhalation:

Key study: Test method was according to OECD guideline 403. The LC50 was greater than 20 mg/L for rats. Further experimental data show LC50 greater than 4800 ppm for different animal species (rats, guinea pigs, rabbits and cats).

Acute toxicity: dermal:

Key study: Test method was similar to OECD guideline 402. The LD50 of sodium trichloroacetate was greater than 2000 mg/kg. This result is supported by further experimental data from the company.

Justification for classification or non-classification

Based on these results, the substance sodium trichloroacetate is not classified for acute toxicity.