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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Additional information

Justification for read-across: a full read-across additional report concerning extrapolation from sodium perchlorate to ammonium perchlorate for genotoxicity endpoint is attached in IUCLID section 13 (CEHTRA 2015).

Ammonium perchlorate was negative in a bacterial gene mutation assay, conducted at the maximal recommended concentration, with and without metabolic activation.

Ammonium perchlorate was negative in a total of three in vivo micronucleus assays, two of which are summarized:

- at up to 1000 mg/kg/day by oral gavage x three days in mice (key study: lethality at 2000 mg/kg once): Sharma 1998

- at up to 500 mg/kg/day by i.p. injection x three days in mice (supportive study: no report; personal communication between Errol Zeiger and EPA; lethality at 1000 mg/kg twice)

- at up to 10 mg/kg/day in drinking water x 90 days in rats (supportive: non-standard, dose too low): Siglin 1998

The read-across analogue substance sodium perchlorate was negative in an in vitro Mouse Lymphoma Assay with and without metabolic activation, up to 5000 µg/mL.


Justification for selection of genetic toxicity endpoint
Several in vitro/in vivo studies were used to complete this endpoint therefore no specific study could be selected.

Short description of key information:
Ammonium perchlorate was negative in a bacterial gene mutation assay, conducted at the maximal recommended concentration.
Ammonium perchlorate was negative in a total of three in vivo micronucleus assays.
The read-across analogue substance sodium perchlorate was negative in an in vitro Mouse Lymphoma Assay with and without metabolic activation, up to 5000 µg/mL.

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

Based on the existence of a negative Ames test, three negative independent in vivo micronucleus assays (including two with maximized top-dose based on lethality) and a negative in vitro Mouse Lymphoma Assay on the read-across analogue substance sodium perchlorate, it was considered that ammonium perchlorate is clearly non-genotoxic (neither mutagenic nor clastogenic).

Considering these data, classification of ammonium perchlorate as mutagenic can be excluded.