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Diss Factsheets
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EC number: 232-188-7 | CAS number: 7789-75-5
- 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
Studies of bacterial mutation (Ames test), cytogenicity and gene mutation in mammalian cells are available for calcium difluoride: additional data are available for other soluble fluoride salts.
Genetic toxicity in vitro
No evidence of mutagenicity was reported in a modern Ames test performed with calcium difluoride (Schulz & Landsiedel, 2010) in Salmonella typhimurium strains TA1535, TA100, TA98, TA1537 and in E. coli strain WP2 uvrA. No evidence of mutagenicity was observed in a recent mammalian cell gene mutation assay (V79/HPRT) performed with calcium difluoride (Wollny, 2010). Likewise, no evidence of cytogenicity was seen in V79 cells in a chromosome aberration test with calcium difluoride (Hall, 2010).
Additionally, a number of studies are available for the read-across source susbtance sodium fluoride. No evidence of mutagenicity was seen with sodium fluoride in an Ames test (NTP, 1990). No evidence of mutagenicity was seen in a mammalian cell mutation assay (V79/HPRT) with sodium fluoride. This study was performed only in the absence of metabolic activation, however this deviation is not considered to be critical as the test substance is not metabolised. A positive result with sodium fluoride is reported in a mouse lymphoma assay (NTP, 1990). Sister chromatid exchange and chromosomal aberrations are reported in an additional NTP study.
Genetic toxicity in vivo
Zeiger et al (1994) report no evidence of clastogenicity, even at dose levels causing severe toxicity, in a well-conducted mouse study performed with sodium fluoride in which chromosomal aberrations and micronucleus formation was assessed.
In contrast, a poorly reported inhalation exposure study performed with HF (Voroshilin et al, 1975) reports clastogenicity in the bone marrow of exposed rats but no dominant lethal effect in exposed mice.
Conclusion
The EU RAR for HF reviews the available data for NaF and HF and concludes that fluoride does not interact directly with DNA and is not genotoxic when administered via an appropriate route (i.e. by oral or inhalation exposure).
Short description of key information:
A negative Ames test, a negative study of cytogenicity in V79 cells
in vitro and a negative study of gene mutation in V79 cells in vitro are
available for calcium difluoride. Some positive studies in vitro are
reported for the more soluble sodium fluoride salt, however reliable in
vivo studies are negative. The available data indicate that fluoride
does not interact directly with DNA and is not genotoxic when
administered via an appropriate route (i.e. by oral or inhalation
exposure).
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
No classification is proposed for genetic toxicity according to the CLP Regulation (1272/2008/EC). The available data indicate that fluoride does not interact directly with DNA and is not genotoxic when administered via an appropriate route (i.e. by oral or inhalation exposure).
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