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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

A not assignable oral repeated dose study in mice cited from ECB IUCLID Dataset ID: 329-01-1, and repeated inhalation studies in rats and mice from a secondary source (only abstract available; original reference in Russian) are available. Additionally results froma secondary source on dermal toxicity (skin effects) are cited.

Key value for chemical safety assessment

Repeated dose toxicity: inhalation - systemic effects

Endpoint conclusion
Dose descriptor:
1.3 mg/m³

Additional information

In the oral repeated dose sutdy the test substance was applied by introduction in the stomach in doses of 1/5, 1/10, and 1/20 LD50 (total cumulative dose= 4.5 times LD50; LD50= 975 mg/kg in rat and mouse) did not provoke the death of animals; an increasing excitement, body weight loss, and respiratory effects were observed. A NO(A)EL was not stated.

The test substance alpha,alpha,alpha-trifluoro-3-tolyl isocyanate was studied on rats and mice which were kept for 4 or 2.5 month, respectively with periodic introduction of alpha,alpha,alpha-trifluoro-3-tolyl isocyanate into the air in exptl. chambers in concentrations of of 1.3, 6.1, and 11.2 mg/m³. At 11.2 mg/m³ the test substance causes functional and histological changes in lungs, liver kidneys, heart, and brain; at 1.3 mg/m³ the test substance is nontoxic for rats and mice. All symptoms of poisoning disappear within 3 months after the experiments are ceased.

Undiluted and as a 10% solution the test substance applied on 5 days once daily induced a pronounced redness with strong skin wrinkles and dryness of skin. A dilution of 5% revealed only for 24 hours a slight rednesson 3 animals. A dilution of 1% exhibited no relevant skin findings.

Justification for classification or non-classification

The oral repeated toxicity study was disregared due to the insufficient documentation of the method and the insufficient information of results.

Due to the results of the dermal and inhalation studies a classification is not justified.