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EC number: 234-585-0 | CAS number: 12013-46-6
- 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
Description of key information
Key value for chemical safety assessment
Skin sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
The key study for skin sensitisation potential of Calcium stannate was tested in a Local Lymph Node Assay (LLNA) with CBA/Ca mice and 5-bromo-deoxyuridine (BrdU (OECD No. 442B) (Hey S., 2010).The test substance was applied as 10 % (w/w), 25 % (w/w) and 50 % (w/w) preparation in vehicle, next to anegative control group treated with 50% propylene glycol (NC) and a positive control group (PC) treated with 25 % (v/v) hexyl cinnamic aldehyde (HCA) in acetone/olive oil (3+1). Four animals per group were treated.25 µL of the selected test substance preparation, reference substance, or vehicle have been applied to the dorsal side of each ear for three consecutive days. No treatment took place on day 4.On day 5 each mouse received BrdU-solution injected intraperitoneally. The animals were sacrificed on day 6 and the draining auricular lymph node from each mouse ear was exercised. A single-cell suspension of the lymph node cells was prepared separately for each animal.
Body weight development of the animals was as expected and within normal ranges. Increases of the ear thickness following test substance application indicating strong irritation properties or symptoms of systemic toxicity were not observed. Only slight symptoms of local irritation at the ears of the highest test substance concentration group and the positive control group were observed.For each treatment group the mean Stimulation Index SI was calculated from the BrdU-labelling indices for each mouse. The Stimulation Indices for Calcium Stannate were lower than 1.6 for all tested concentrations. The positive control showed a clear positive response (SI≥1.6) indicating the adequate function of the test system. From the test results it is concluded that the test substance Calcium stannate has no sensitising properties under the given experimental conditions.
Migrated from Short description of key information:
The test substance Calcium Stannate was tested regarding its skin sensitisation potential in a Local Lymph Node Assay (LLNA) with CBA/Ca mice and 5-bromo-deoxyuridine (BrdU) to measure lymphocyte proliferationa (OECD No. 442B). From the test results it is concluded that the test substance Calcium stannate has no sensitising properties under the given experimental conditions.
Justification for classification or non-classification
As there is no sensitisation potential in the LLNA test, classification is not warranted.
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