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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

- Acute oral toxicity: ACD/Percepta predicted for ADPA an acute oral LD50 to mouse equal to 1000 mg/kg and an acute oral LD50 to rat equal to 750 mg/kg. 

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
adverse effect observed
Dose descriptor:
LD50
Value:
750 mg/kg bw
Quality of whole database:
Two ACD/Percepta prediction are available (WoE, Kr. 2).The prediction is considered of moderate reliability.

Additional information

ACD/Percepta predicted for ADPA an acute oral LD50 to rat equal to 750 mg/kg. The prediction is considered of moderate reliability (RI in range 0.5 - 0.75). ACD/Percepta predicted for ADPA an acute oral LD50 to mouse equal to 1000 mg/kg. The prediction is considered of moderate reliability. Based on these data, ADPA is considered as harmful if swallowed.


Justification for selection of acute toxicity – oral endpoint
The lowest LD50 predicted for ADPA was 750 mg/kg bw in rat.

Justification for classification or non-classification

ACD/Percepta predicted for ADPA an acute oral LD50 to mouse equal to 1000 mg/kg and an acute oral LD50 to rat equal to 750 mg/kg. Based on these data, ADPA is considered as harmful if swallowed and classified into Category. 4 (H302) according to CLP Regulation (1272/2008) criteria.