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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Repeated dose toxicity: via oral route - systemic effects

Link to relevant study records
Reference
Endpoint:
repeated dose toxicity: oral
Remarks:
other: read -across from 90 days study an analogue
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The analogue shares the same finctional group with Ammmonium carbonate.
Principles of method if other than guideline:
Read across on analogue substance.
GLP compliance:
no
Dose descriptor:
NOAEL
Effect level:
1 256 mg/kg bw/day (nominal)
Based on:
test mat.
Critical effects observed:
not specified
Conclusions:
NOAEL (90days)=1256mg/kg bw.
Executive summary:

NOAEL (90days)=1256mg/kg bw.

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
NOAEL
1 256 mg/kg bw/day

Additional information

Justification for classification or non-classification

NOAEL =1256mg/kg bw, the substance is not classified.