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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
acute toxicity: inhalation
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
the study does not need to be conducted because exposure of humans via inhalation is not likely taking into account the vapour pressure of the substance and/or the possibility of exposure to aerosols, particles or droplets of an inhalable size
Justification for type of information:
JUSTIFICATION FOR DATA WAIVING
Waived based on a low vapour pressure of 0.0005 Pa at 25°C. In accordance with Annex VIII of Regulation (EC) 1907/2006 (REACH), section 8.5.2 it is considered justified to omit the acute toxicity by inhalation as testing by this route is inappropriate. Exposure via the inhalation route is not relevant due to the substance being a liquid with a very low vapour pressure. Such liquids require strong measures to be taken to generate airborne particulates of sufficiently high respirability. Consequently the acute oral and acute dermal studies are more applicable to the evaluataion of acute toxicity and relavence to human exposure. In addition, a supporting publication by Knaak et al (1997) "Toxicology of Mono-, Di-, and Triethanolamine" documented an acute inhalation study with triethanolamine in which the low vapour pressure limited the technically highest attainable concentration to ca. 1.8 mg/m3 (0.29 ppm).

Data source

Materials and methods

Results and discussion

Applicant's summary and conclusion