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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Acute toxicity: oral:
A K2 acute oral toxicity test was performed in female Sprague-Dawley rats according to a guideline similar to OECD Guideline 401 (Bruce DW, 1963). This study was selected as key study since this is the only available reliable study (K2).

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
LD50
Value:
2 750 mg/kg bw

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Acute toxicity: oral

Bruce DW (1963) investigated the acute oral toxicity via gavage of a single oral dose of neodymium nitrate in 5 to 10 female Sprague-Dawley rats. The animals were observed for 30 days although no deaths occurred later than 4 days after administration. Within 1 to 2 hours after oral administration of the rare earth nitrate most of the rats were depressed, and animals that received lethal doses showed little activity during the survival period. Throughout the observation period no gross pathologic changes were noted. The acute oral LD50 of neodymium nitrate in female rats was determined to be 2750 mg/kg. This study is considered key study.

Another publication was identified (Lewis 1995) but it is a secondary source of Bruce (1963). Therefore it is scored as K4.

No data were available for the inhalation and dermal route.


Justification for selection of acute toxicity – oral endpoint
Only K2 available. No classification needed on the basis of the effect level.

Justification for classification or non-classification

Based on the results of the acute oral toxicity study and according to the criteria of the DSD and CLP Regulation, neodymium trinitrate should not be classified as an acute oral toxicant.

No data were available to decide on the classification for the inhalation and dermal route.