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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Several studies available

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Additional information

For the read across substances FeNaEDDHA and FeNaEDDHMA (see section 13) several studies are available:

acute oral toxicity: LD50 > 2000 mg/kg bw or > 5000 mg/kg bw

acute inhalation toxicity: 4 -h LC50 > 4200 or >1240 mg/m3 (technically highest available concentrations)

acute dermal toxicity: LD50 > 2000 mg/kg bw

Justification for classification or non-classification

Based on the data available for the read across substances FeNaEDDHA and FeNaEDDHMA, there is no need to classify FeKEDDHA as acute toxic via the oral, dermal or inhalation route of exposure.