Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 accordance with Column 2 of REACH Annex VII, information requirement section 8.5.1, 8.5.2 and 8.5.3 the acute toxicity studies by the oral, dermal and inhalation routes do not need to be conducted as the substance is classified as corrosive to the skin.


 

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records
Reference
Endpoint:
acute toxicity: oral
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
the study does not need to be conducted because the substance is classified as corrosive to the skin
Justification for type of information:
In accordance with Column 2 of REACH Annex VII, information requirement section 8.5.1, this study does not need to be conducted as the substance is classified as corrosive to the skin.
Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via inhalation route

Link to relevant study records
Reference
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 the substance is classified as corrosive to the skin
Justification for type of information:
In accordance with Column 2 of REACH Annex VIII, information requirement section 8.5.2, this study does not need to be conducted as the substance is classified as corrosive to the skin.
Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Quality of whole database:
Single study on a read-across substance conducted according to a standardised guideline and in compliance with GLP.

Additional information

Justification for classification or non-classification

In accordance with the criteria for classification as defined in Annex I, Regulation (EC) No 1272/2008, the material does not require classification with respect to acute toxicity.