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EC number: 405-290-6 | CAS number: 12036-37-2
- 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
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 24 April 1989 - 26 April 1989
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Read across to similar substance. Study conducted to GLP in compliance with agreed protocols, with no or minor deviations from standard test guidelines and/or minor methodological deficiencies, which do not affect the quality of the relevant results.
- Justification for type of information:
- See read-across justification in Section 13.
- Reason / purpose for cross-reference:
- other: Target substance
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Vehicle:
- yes
- Details on test solutions:
- Preliminary solution in 1 % Tween 80-acetone
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Test Species
Name: Daphnia magna (Straus).
Culture: At 20 ± 2 °C in glass vessels containing two litres of dechlorinated and aged tap water. Cultures were fed daily with a mixture of fry fish food (Liquifry) and a suspension of mixed algae (predominantly Chlorella spp.). Culture conditions ensured that reproduction was by parthenogenesis.
Selection: Gravid adults were isolated 24 hours prior to initiation of the test. Young daphnids produced overnight were used for testing. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- Total hardness approximately 50 mg/L as CaCO3.
- Test temperature:
- 21 °C
- pH:
- pH 7.7 - 7.8
- Dissolved oxygen:
- At 0 hours 8.5 - 8.6 mgO2/L. At 48 hours 8.3 - 8.4 mgO2/L
- Nominal and measured concentrations:
- Nominal concentration of 0.10 mg/L
- Details on test conditions:
- Test Water
Dechlorinated (with sodium thiosulphate) and aged laboratory tap water. Total hardness approximately 50 mg/L as CaCO3.
Exposure Conditions
Test vessels: Glass jars each containing 200 mL test solution.
Experimental design: 1 test concentration, 4 replicates, plus 1 control and 1 solvent control (including 100 µL/L auxiliary solvent) each in duplicate. 40 animals per concentration.
Method of initiation: Daphnia were placed in the test solutions after addition of the test substance.
Loading: 20 mL test solution per organism.
Photoperiod: 16h light, 8h dark.
Temperature: 21 °C
Aeration: None
Test concentration: 0.10 mg/L, 4 replicates.
Medium renewal: None.
Duration of exposure: 48 hours.
Criteria of effect: Daphnia were considered to be immobilised if they were unable to swim for approximately 15 seconds after gentle agitation. - Reference substance (positive control):
- no
- Duration:
- 24 h
- Dose descriptor:
- NOEC
- Effect conc.:
- > 0.1 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- > 0.1 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- There were no mortalities in 40 daphnids exposed to a nominal test concentration of 0.10 mg/L for a period of 48 hours. 0.10 mg/L was the highest test concentration that could be prepared due to the low water solubility of the test material and having regard to the amount of auxiliary solvent permitted in the test.
0.10 mg/L was the highest concentration tested as the test material was observed to precipitate/settle out over a 24-hour period, in the range finding test, at higher test concentrations.
Care should be taken in the interpretation of these results as the verification of test concentrations showed that the average test concentration was 23 % of nominal i.e. 0.023 mg/L after 48 hours and it is recommended that this level be taken as the true exposure level. However, the material was shown to be chemically stable in water.
The 0 hour values were omitted from the calculation of percentage of nominal values to give a "worst case" analysis of the data. The decrease in test concentrations is considered to be due to precipitation and/or settlement.
Other combinations of the various recognised auxiliary solvents and mixtures of Tween 80 (up to 20 % Tween in solvent) were used during the range finding experiments, however, the combination of 1 % Tween 80-acetone was found to give the best testable dispersion of the test material. - Validity criteria fulfilled:
- yes
- Conclusions:
- 48 h NOEC > 0.10 mg/L
- Executive summary:
48 h NOEC > 0.10 mg/L was found under static test conditions according to OECD Guideline No. 202, Part 1 and EEC Directive 67/548 Annex V C.2 as published in 84/449/EEC.
Reference
Cumulative Immobilisation Data for Daphnia Magna Exposed for 48 Hours
Concentration (mg/L) |
Cumulative immobilised Daphnia (initial population: 10) |
|||||
24 hours |
48 hours |
|||||
|
Total |
% |
|
Total |
% |
|
Control R1 R2
Solvent Control R1 R2
0.10 R1 R2 R3 R4 |
0 0
0 0
0 0 0 0 |
0
0
0 |
0
0
0 |
0 0
0 0
0 0 0 0 |
0
0
0 |
0
0
0 |
R1 – R4: Replicates 1, 2, 3, and 4
Description of key information
A 48 h NOEC of >0.10 mg/L was obtained in a static test conducted on Daphnia magna using the read-across substance Zinc Hydroxystannate.
Key value for chemical safety assessment
Additional information
The short term toxicity of the read-across substance Zinc Hydroxystannate to Daphnia magna was investigated in a 48 hour static test conducted in accordance with GLP and the standardised guidelines OECD Guideline No. 202, Part 1 and EEC Directive 67/548 Annex V C.2 as published in 84/449/EEC.
0.10 mg/L was the highest test concentration that could be prepared due to the limited water solubility of the test material and having regard to the limitations on the amount of auxiliary solvent permitted in the test (100 µL/L of 1 % Tween -80 in acetone).
A 48 h NOEC of >0.10 mg/L was found under the conditions of this study.
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