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EC number: 215-248-7 | CAS number: 1314-95-0
- 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

Sediment toxicity
Administrative data
Link to relevant study record(s)
- Endpoint:
- sediment toxicity: short-term
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Justification for type of information:
- Both substances contain the same ion (tin(II)) as active substance. Tin dichloride is significantly better water soluble when compared to tin sulfide. Further information is provided in the read across justification.
- Reason / purpose for cross-reference:
- read-across source
- GLP compliance:
- no
- Duration:
- 48 h
- Dose descriptor:
- LC50
- Effect conc.:
- 69.7 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 38.1 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Details on results:
- LC50: 38.1 mg/L (95% C.I.: 30.5-41.7 mg /L)
- Reported statistics and error estimates:
- probit analysis
- Validity criteria fulfilled:
- not specified
- Conclusions:
- Tubifex tubifex 96h-LC50: 38.1 mg/L
- Executive summary:
In an acute study, the acute toxicity of tin dichloride on Tubifex tubifex has been determined by Fargasova (1994). The test was performed similar to OECD 235. The result was based on dissolved tin ions. The 96-hour LC50 based on tin(II) is 30.0 mg/L.
Based on the molecular masses, the expected toxicity of tin sulfide was calculated to be 38.1 mg/L. This is more than a factor of 500000 above the limit of water solubility of tin sulfide. Hence it can be concluded that tin sulfide will have no acute toxic effects on Tubifex tubifex.
- Endpoint:
- sediment toxicity: short-term
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Justification for type of information:
- Both substances contain the same ion (tin(II)) as active substance. Tin dichloride is significantly better water soluble when compared to tin sulfide. Further information is provided in te read across justification.
- Reason / purpose for cross-reference:
- read-across source
- Duration:
- 48 h
- Dose descriptor:
- LC50
- Effect conc.:
- 10.541 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 4.572 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Details on results:
- In the source study, the toxicity with tin dichloride was reported as LC50: 3.6 mg Sn/L (95% C.I.: 3.0-4.2 mg Sn /L)
Molecular mass:
Sn: 118,710 g/mol (rounded)
S: 32,06 g/mol (rounded)
molecular mass of tin sulfide; 150.775 g/mol
The hypothetical toxicity of tin sulfide was calculated as
LC50 (based on Sn(II) )*molecular mass of tin sulfide / molecular mass of tin=LC50 (based on tin(II))*1.27
Example:
The LC50 for tin(II) is 3.6 mg/L. This corresponds to 4.572 mg/L tin sulfide. - Reported statistics and error estimates:
- probit analysis
- Validity criteria fulfilled:
- not specified
- Conclusions:
- Chironomus plumosus 96h-LC50: 4.572 mg/L
- Executive summary:
In an acute study, the acute toxicity of tin dichloride on Chironomus plumosus has been determined by Fargasova (1994). The test was performed similar to OECD 235. The result was based on dissolved tin ions. The 96-hour LC50 based on tin(II) is 3.6 mg/L.
Based on the molecular masses, the expected toxicity of tin sulfide was calculated to be 4.572 mg/L.
This is more than a factor of 5000 above the limit of water solubility of tin sulfide. Hence it can be concluded that tin sulfide will have no acute toxic effects on Chironomus plumosus.
Referenceopen allclose all
Description of key information
In an acute study, the acute toxicity of tin dichloride on Chironomus plumosus has been determined by Fargasova (1994). The test was performed similar to OECD 235. The result was based on dissolved tin ions. The 96-hour LC50 based on tin(II) is 3.6 mg/L. Based on the molecular masses, the expected toxicity of tin sulfide was calculated to be 4.572 mg/L. This is more than a factor of 5000 above the limit of water solubility of tin sulfide. Hence it can be concluded that tin sulfide will have no acute effects on Chironomus plumosus.
In an acute study, the acute toxicity of tin dichloride on Tubifex tubifex has been determined by Fargasova (1994). The test was performed similar to OECD 235. The result was based on dissolved tin ions. The 96-hour LC50 based on tin(II) is 30.0 mg/L. Based on the molecular masses, the expected toxicity of tin sulfide was calculated to be 38.1 mg/L. This is more than a factor of 500000 above the limit of water solubility of tin sulfide. Hence it can be concluded that tin sulfide will have no acute toxic effects on Tubifex tubifex.
Key value for chemical safety assessment
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