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EC number: 701-315-2 | CAS number: -
- 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
- Data waiving:
- study scientifically not necessary / other information available
- Justification for data waiving:
- the study does not need to be conducted because the substance is highly insoluble in water, hence indicating that aquatic toxicity is unlikely to occur
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- documentation insufficient for assessment
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Version / remarks:
- Rangefinder only
- Principles of method if other than guideline:
- Rangefinder test for acute Daphnia study
- GLP compliance:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: All test concentrations and control at test start and test end
- Sample storage conditions before analysis: Pt samples were acidified with HNO3 for stabilisation and analysed immediately unless technically not possible. Samples were analysed for the organic ligand immediately after being taken - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: The stock solution was prepared in dilution water by adding 30 mg of test item to 3 L dilution water resulting in a nominal concentration of 10 mg/L. The test solution was stirred by using a magnetic stirring bar for 1 hour at room temperature (ca. 20 °C). The stock solution was filtered with a PES filter. The individual test solutions were prepared by diluting the stock solution with dilution water.
- Controls: Dilution water
- Solvent: None - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM:
- Source: German Federal Environment Agency, Institut für Wasser-, Boden- und Lufthygiene. Specimens used in the test were bred in the laboratory of the Fraunhofer IME.
- Feeding during test: None
- Age at test start: 4 - 24 hours old - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- 70 - 120 mg/L CaCO3
- Test temperature:
- Not reported
- pH:
- Mean temperature: 20.8°C
- Dissolved oxygen:
- 7.8 - 10.3 mg/L
- Nominal and measured concentrations:
- Nominal concentrations: 0.1, 1 and 10 mg/L
Measured Pt concentrations:Measured concentrations of organic ligand: - Details on test conditions:
- TEST SYSTEM
- Test vessel: 50 mL glass beakers with 50 mL test solution covered with glass panes
- Aeration: None
- No. of organisms per vessel: 5
- No. of vessels per concentration: 4
- No. of vessels per control: 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Purified drinking water
OTHER TEST CONDITIONS
- Light intensity: 937 - 949 lux
EFFECT PARAMETERS MEASURED: Number of dead animals, abnormalities in appearance and behaviour monitored daily
RANGE-FINDING STUDY
- Test concentrations: 0.1, 1 and 10 mg/L- Reference substance (positive control):
- yes
- Remarks:
- K2Cr2O7 tested twice a year
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 10 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: No effects at highest concentration tested
- Validity criteria fulfilled:
- yes
- Conclusions:
- At the highest test concentration of 10 mg L-1, no immobility was observed.
- Executive summary:
Simon (2016) is a non-GLP range-finder study with Daphnia magna. A 48 -hour static study was conducted. Analytical verification of both platinum and the organic ligand showed that none of the organic ligand could be detected (LOQ: 0.0025 mg/L) and very small amounts of platimum were detected in solution. At the highest test concentration of 10 mg L-1, no immobility was observed. As the test item was shown to be very poorly soluble in the range-finder study, and it was not possible to get higher amounts of test item into solution following further solubility trials, and no effects were observed at the highest nominal concentration tested, a definitive test was not conducted.
Referenceopen allclose all
Description of key information
A range-finder study showed no toxicity at nominal concentrations up to 10 mg L-1 (highest concentration tested). Analytical monitoring of both the organic ligand and platinum showed very low concentrations of platinum and none of the organic ligand could be detected in solution. As the test item is very poorly soluble, and it was not possible to get more of the test item into solution, aquatic toxicity is not expected at the limit of solubility and this was demonstrated in the range-finding study.
Key value for chemical safety assessment
Additional information
A range-finder study showed no toxicity at nominal concentrations up to 10 mg L-1 (highest concentration tested). Analytical monitoring of both the organic ligand and platinum showed very low concentrations of platinum and none of the organic ligand could be detected in solution. As the test item is very poorly soluble and it was not possible to get more of the test item into solution, aquatic toxicity is not expected at the limit of solubility and this was demonstrated in the range-finding study.
Karstedt concentrate was tested in range-finder studies with fish, Daphnia and algae (Eilebrecht 2016, Simon 2016, Wenzel 2016). The highest nominal test concentration used in the range-finders was 10 mg L-1. The highest concentration test solutions were prepared by adding the test item to test media (20 mg in 2 litres), stirring for one hour and then passing the resulting ‘solution’ through a 0.2 µm PES filter. The filtrate was used directly as the highest test concentration (nominally 10 mg L-1), while the lower test concentrations were prepared by appropriate dilution of the filtrate. This procedure ensured that only soluble components of the test item were assessed for toxicity. The resulting test solution at the highest concentration used in the range-finder is considered to be at the limit of solubility for the substance. Analytical monitoring of the test solutions was conducted, with both the organic ligand and platinum measured. In the range-finding studies, only very low concentrations of platinum were detected and the organic ligand was present close to or below the LOQ in all samples. No toxicity was observed for fish,Daphniaor algae.
As the substance was shown to be poorly soluble in test media and therefore only small amounts of platinum could be detected in the range-finder studies, further solubility trials were conducted in order to determine if it is possible to increase the concentrations of the test item components in solution. Although higher solubility was determined for the test item in a water solubility study, the water solubility result was based on analysis of platinum only, and similar levels of solubility were not observed with ecotoxicity test media. 96-hour solubility trials were conducted using the same media used in the fish and Daphnia studies, adjusted to pH 6, and with three different separation techniques trialled (decanting, filtering and centrifugation). An initial concentration of 4.3 mg L-1Karstedt concentrate was used. The test solutions were analysed after 0, 24, 48, 72 and 96 hours. The organic ligand was present close to or below the LOQ in all samples (LOQ 2.16 µg L-1), suggesting it is highly insoluble and therefore unlikely to be toxic to aquatic organisms. Platinum was detected in the solutions but measured concentrations were low, ranging from 3.90 to 9.43 µg Pt L-1over the course of the test for filtered and centrifuged solutions. Measured concentrations were higher for the decanted solutions (45.16 µg Pt L-1at 0 hours to 7.03 µg Pt L-1at 96 h), however it is believed that this is likely to be due to some of the undissolved test material being included during the decanting phase.
Based on the solubility trials, it was not possible to get the organic ligand into solution and only small amounts of platinum were in solution. The platinum concentrations in solution are unlikely to lead to aquatic toxicity. Comparing the measured concentrations of platinum from the filtered and centrifuged solutions against the acute environmental reference values (ERV) for other platinum substances (481 µg L-1for dihydrogen hexahydroxyplatinate, 117 µg L-1for dihydrogen hexahydroxyplatinate, compound with 2-aminoethanol, 108 µg L-1for diammonium hexachloroplatinate, 7600 µg L-1for tetraammineplatinum hydrogencarbonate, 9750 µg L-1for platinum tetraamine diacetate and 20.5 µg L-1for hexachloroplatinic acid) shows that measured platinum concentrations released from Karstedt concentrate are lower than the ERVs and therefore aquatic toxicity is not expected. The most toxic platinum substance, hexachloroplatinic acid, is expected to release platinum in the form of chloroplatinate anions and, although the exact form of platinum released from Karstedt concentrate is not known, it is not expected to be chloroplatinate. Any platinum released from Karstedt concentrate is therefore likely to be in a less toxic form than that released from hexachloroplatinic acid. However, even comparing the platinum release from the solubility trial against the acute ERV for hexachloroplatinic acid, as a worst case approach, aquatic toxicity from Karstedt concentrate is not expected.
Analysis of the organic ligand showed that it was present close to or below the LOQ in all samples, although the fate of the ligand is not clear. The ligand may be very poorly soluble and therefore removed during filtering of the solutions (it appears that solubility of Karstedt concentrate in test media is lower than solubility of the organic ligand alone), it may be strongly adsorbing to the test vessels or filters, although several different methods for preparing the test solutions have been trialled in order to reduce this possibility, or it may hydrolyse leading to breakdown products that are not detected in the analysis. If breakdown products are present these are not considered to contribute to the toxicity of the test item as the breakdown products would also have been present in the range-finder tests in which no toxicity was observed.
Based on the results from solubility trials it is concluded that neither the organic ligand nor the platinum component of Karstedt concentrate will enter solution in high enough amounts to lead to aquatic toxicity. This is supported by the results of the range-finder studies conducted with three trophic levels at a highest nominal concentration of 10 mg L-1. As it is not possible to get more of the test item in solution, conducting definitive ecotoxicity studies is not considered to be necessary. To conclude on environmental classification, the standard approach would be to test up to a nominal concentration of 100 mg L-1. However, for this substance testing at a nominal concentration of 100 mg L-1 is considered to be unnecessary, as the limit of solubility appears to have been reached at the nominal concentration of 10 mg L-1, and testing at higher concentrations would not lead to additional test item in solution. As no toxicity was observed at the limit of solubility in the range-finder studies, neither an acute or chronic environmental classification is considered to be required for the substance.
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