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Diss Factsheets
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EC number: 231-912-9 | CAS number: 7778-74-7
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
Limited data are available and mostly come from secondary sources. The ATSDR Review of perchlorate toxicity (US EPA, 2008) concludes that the available data suggest that perchlorate is not a mutagenic or clastogenic agent. Cited in vitro data include a negative study of the induction of the SOS response in Salmonella typhimurium strain TA1535, a negative assay for the induction of DNA-protein crosslinks in cultured human lymphocytes and the absence of reverse mutation in an Ames test performed in six strains of Salmonella typhimurium. A negative response is also reported in a mouse lymphoma assay performed in the absence and presence of metabolic activation.
In vivo data are limited to a negative mouse bone marrow micronucleus assay performed at dose levels of up to 500 mg/kg bw (on three consecutive days by intraperitoneal injection). It is also notable that the 90-day oral toxicity study (Siglin et al, 2000) did not identify any increase in the proportion of micronucleated bone marrow PCEs following treatment with ammonium perchlorate at dose levels of up to 10 mg/kg bw/d administered in the drinking water.
A second published review (Mattie et al, 2006; Perchlorate Toxicity and Risk Assessment, United States Air Force Research / United States Department of Defense) also concludes that ‘genotoxicity assays showed that perchlorate has no toxic effects on genes or chromosomes in cells’. The therapeutic use of perchlorate salts (including potassium perchlorate) in humans for the treatment of hyperthyroidism over several decades also indicates an absence of genetic toxicity.
The available data therefore indicate that potassium perchlorate is not genotoxic.
Justification for selection of genetic toxicity endpoint
Higher tier sudy confirming the weight of evidence from review papers
Short description of key information:
Data are limited to review papers and confirmed by an absence of micronucleus induction in the 90-day toxicity study.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
The available data indicate that potassium perchlorate is not genotoxic; no classification is proposed.
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