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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

In a rat 4-hour acute inhalation study, it was suggested that the test substance was irritating to respiratory tract tissue (mucous membrane) due to nasal discharge observed in all exposure groups.

Key value for chemical safety assessment

Respiratory irritation

Endpoint conclusion
Endpoint conclusion:
adverse effect observed (irritating)

Additional information

In accordance to REACH Annex XI Section 2; information requirement section 8.1.1 guideline testing for skin or eye irritation is technically not feasible because the test substance is a gas. In a rat 4-hour acute inhalation study, it was suggested that the test substance was irritating to respiratory tract tissue (mucous membrane) due to nasal discharge observed in all exposure groups.


Effects on respiratory irritation: irritating

Justification for classification or non-classification

Data lacking due to waiving arguments, so substance cannot be classified for skin or eye irritation according to the EU Directive 67/548/EEC and EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008. Due to nasal discharge (irritation) in the acute inhalation study, the substance is classified for respiratory irritation Xi;R37 (irritating to respiratory system) according to EU Directive 67/548/EEC and STOT SE 3 according to EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008.