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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Repeated dose toxicity: oral. Key studies: Read-across: experimental results with the substance sodium trichloroacetate.

Key value for chemical safety assessment

Additional information

Repeated dose toxicity: oral. Key studies: Read-across: experimental results with the substance sodium trichloroacetate.

Free trichloroacetic acid is a strong organic acid, which forms water-soluble salts with bases. In any medium at or near neutral pH the predominant form present is the trichloroacetate anion. The salts are therefore expected to be toxicologically equivalet to the free acid, except for the acute corrosive properties, which are at least partly determined by the very low pH of strong solutions of the acid.

In a 90-day study with dogs, from 2000 ppm upwards effects were observed in mortality, body weights, haematology, urinalysis, gross pathology and histopathology. Therefore, the NOEL was determined to be 500 ppm (approximately 30 mg/kg bw/day).

In a 4-month study with rats, the NOEL was determined to be 4000 ppm (approximately 365 mg/kg bw/day), based on body weight reduction observed at 10000 ppm.

In a 2-year study in rats, the NOEL was determined as 1600 ppm (approximately 80 mg/kg bw/day), based on a significantly body weight reduction observed at 10000 ppm.

Based on the molecular weights, the NOELs for trichloroacetic acid would be as follows:

- 90 -day study with dogs: 26 mg/kg bw/day.

- 4 -month study with rats: 322 mg/kg bw/day.

- 2 -year study in rats: 70.5 mg/kg bw/day

Justification for classification or non-classification

Based on the results obtained in the different repeated dose toxicity studies, the substance is not classified for specific target organ toxicity.