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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
LD50
Value:
2 000 mg/kg bw
Quality of whole database:
code 1 (reliable without restriction)

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
LD50
Value:
2 000 mg/kg bw
Quality of whole database:
code 1 (reliable without restriction)

Additional information

Justification for selection of acute toxicity – oral endpoint
No mortality and no systemic signs. Substance of low oral toxicity. No classification required.

Justification for selection of acute toxicity – inhalation endpoint
As a solid in solution, test substance is unlikely to absorbed by inhalation. In the the case of normal use, aerosols cannot be produced and test substance is not volatile

Justification for selection of acute toxicity – dermal endpoint
No mortality and no systemic signs. Substance of low dermal toxicity. No classification required.

Justification for classification or non-classification

No mortality and no systemic signs. Substance of low oral and dermal toxicity. No classification required.