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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

The target substance was tested negative for acute dermal irritating properties in rabbits in a study according to OECD 404. In contrast, the target substance caused severe eye irritating effects in an acute eye irritation/corrosion study in rabbits (OECD 405).

Key value for chemical safety assessment

Skin irritation / corrosion

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (not irritating)

Eye irritation

Endpoint conclusion
Endpoint conclusion:
adverse effect observed (irreversible damage)

Respiratory irritation

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

The target substance was tested negative for acute dermal irritating properties according to OECD 404. The non-irritating properties of the target substance to the skin are supported by a suitable read across partner, which was tested also negative in an in vivo acute dermal irritating study conducted in accordance with OECD 404. In contrast, the target substance was severely irritating to the eyes of rabbits in an acute eye irritation study (OECD 405). Based on these results, the test substance is considered to be not irritating to skin, but severely irritating/corrosive to the eye.

Justification for classification or non-classification

The target substance did not cause any skin effects in acute dermal irritating studies according to OECD test guideline 404. Therefore, the target substance does not warrant classification for skin irritation.

In contrast, the test item was severely irritating to the eyes of rabbits in an OECD 405 study. The application of the substance to the eye of rabbits led to an irreversible effect of the corneal opacity within 21 days observation period. Therefore, the test item meets the classification criteria according to the CLP regulation. The target substance is classified for irreversible effects on the eye (Category 1, H318).