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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
acute toxicity: dermal
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
the study does not need to be conducted because the physicochemical and toxicological properties suggest no potential for a significant rate of absorption through the skin
Justification for type of information:
The EU risk assessment report for edetic acid states:
"No data are available on acute dermal toxicity. Taking into account the poor dermal absorption
(Foremann, 1954), there is reason to assume that the result of an acute dermal toxicity test would
not reveal toxic properties warranting a classification and labelling for acute dermal toxicity."

"Because of the very low activity, the urine from skin absorption studies
required special treatment with the sodium salt of EDTA as carrier. The maximum of activity in
the urine after application over an area of 100 cm² was 0.001%."

Data source

Materials and methods

Results and discussion

Applicant's summary and conclusion