Registration Dossier

Administrative data

Description of key information

The substance has not been tested.
The Disciminating dose levels are based on a surrogate read-across substance.

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
discriminating dose
5 000 mg/kg bw

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Additional information

The substance is unstable in water and moist atmosphere and testing would record the results of the key degradation products.These are titanium dioxide, propan-2-ol, triethanolamine and propylene glycol. These are all well evaluated low-hazard substances and further animal testing is not justified.


Justification for selection of acute toxicity – inhalation endpoint
At high concentrations, propan-2-ol will cause drowsiness

Justification for classification or non-classification