Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 268-717-3 | CAS number: 68133-90-4
- 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 fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 38.5, 84.7, 186.4, 410.0 and 902.0 HPPA-2AE/L (nominal)
- Sampling method: Not stated
- Sample storage conditions before analysis: For analysis of Pt, the samples were acidified with HNO3 and immediately stored at 4°C until analysis. For analysis of 2AE, samples were immediately stored at ≤8°C until analysis. - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: A stock solution was prepared by dissolving test item in dilution water and stirring for one hour. The stock solution was filtered before use in the test and then diluted with dilution water to obtain the test concentrations.
- Controls: Dilution water
- Chemical name of vehicle (organic solvent, emulsifier or dispersant): None
- Concentration of vehicle in test medium (stock solution and final test solution(s) or suspension(s) including control(s)): None
- Evidence of undissolved material (e.g. precipitate, surface film, etc.): Filtered to remove undissolved solid Pt.
- Extraction recovery (indicate if results are corrected or not for recoveries):
2AE: mean recoveries of samples 56.18-58.46%
Pt: 100.0-101.3%
- Method of confirmation of identity of measured compound:
2AE: Reference sample
Pt detected at wavelengths of 214.424 nm (range finder test), 177.648 (definite test) with no interferences observed. - Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- TEST ORGANISM
- Common name: Zebrafish
- Strain: Teleostei, Cyprinidae
- Source: Test facility bred
- Age at study initiation (mean and range, SD): Not stated
- Length at study initiation (length definition, mean, range and SD): 1.6 - 1.9 cm
- Weight at study initiation (mean and range, SD): 0.024 - 0.044 g
- Method of breeding: Not stated
- Maintenance of the brood fish: Not stated
ACCLIMATION
- Acclimation period: at least 12 days
- Acclimation conditions (same as test or not): Same as test
- Type and amount of food during acclimation: Live brine shrimp (Artemia salina) nauplii and ground flake food TetraMin.
- Feeding frequency during acclimation: shrimp - ad libitum, flake food – once daily
- Health during acclimation (any mortality observed): Mortality of the batch was less than 5 % in the week preceding the start of the study.
FEEDING DURING TEST
- Food type: None
- Amount: None
- Frequency: None - Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Hardness:
- 1.2 mmol/L
- Test temperature:
- 23.0 - 23.1 °C
- pH:
- 8.06 - 8.66
- Dissolved oxygen:
- 110 %
- Salinity:
- Not applicable
- Nominal and measured concentrations:
- Nominal concentration: 38.5, 84.7, 186.4, 410.0, and 902.0 mg HHPA-2AE/L, corresponding to nominal platinate (Pt) concentrations of 6.6, 14.5, 32.0, 70.3, and 154.7 mg/L. The nominal concentrations of 2-amino-ethanol (2AE), which was present in a molecular ratio (Pt:2AE) of 1:2, were 4.1, 9.1, 20.0, 44.0, and 96.9 mg/L.
Arithmetic mean measured Pt concentrations: 0.4, 1.0, 2.2, 5.0, 11.1 mg/L
Arithmetic mean measured 2-AE concentrations: 2.4, 5.2, 11.6, 25.0, 55.1 mg/L - Details on test conditions:
- TEST SYSTEM
- Test vessel: Beakers
- Type: open
- Material, size, headspace, fill volume: Full glass beakers of 2.5 L, containing 2.0 L of test solution
- Aeration: Yes, via glass capillaries
- Renewal rate of test solution (frequency/flow rate): Semi-static system, test solutions replaced after 48 hours.
- No. of organisms per vessel: 7
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
- No. of vessels per vehicle control (replicates): Not applicable
- Biomass loading rate: 1 g/L
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Purified drinking water
- Total organic carbon: NPOC 0.5895 mg/L
- Particulate matter: Not stated
- Metals:
cadmium [μg/L] < 0.674
chrome [μg/L] < 0.623
copper [μg/L] < 5.08
iron [μg/L] < 1.14
manganese [μg/L] < 0.699
nickel [μg/L] < 1.24
lead [μg/L] < 1.74
zinc [μg/L] 2.13
- Pesticides: Not stated
- Chlorine: <0.02 mg/L
- Alkalinity: 1.8 mmol/L
- Ca/mg ratio: 5 mmol/L
- Culture medium different from test medium: None
- Intervals of water quality measurement: Not stated
OTHER TEST CONDITIONS
- Adjustment of pH: None
- Photoperiod: light dark cycle 12/12 hours
- Light intensity: Not stated
EFFECT PARAMETERS MEASURED (with observation intervals if applicable): Mortality, length and weight
TEST CONCENTRATIONS
- Spacing factor for test concentrations: Not stated
- Justification for using less concentrations than requested by guideline: Not applicable
- Range finding study: No
- Test concentrations: Nominal concentration: 38.5, 84.7, 186.4, 410.0, and 902.0 mg HHPA-2AE/L, corresponding to platinate (Pt) concentrations of 6.6, 14.5, 32.0, 70.3, and 154.7 mg/L. The nominal concentrations of 2-amino-ethanol (2AE), which was present in a molecular ratio (Pt:2AE) of 1:2, were 4.1, 9.1, 20.0, 44.0, and 96.9 mg/L.
- Results used to determine the conditions for the definitive study: Not stated - Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 55.1 other: mg 2AE/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- other: 2AE
- Basis for effect:
- mortality (fish)
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 11.1 other: mg Pt/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- element
- Basis for effect:
- mortality (fish)
- Details on results:
- - Behavioural abnormalities: None
- Observations on body length and weight: No effect
- Other biological observations: None
- Mortality of control: None
- Other adverse effects control: None
- Abnormal responses: None
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: None
- Effect concentrations exceeding solubility of substance in test medium: None - Reported statistics and error estimates:
- No statistical analysis was performed as there was no mortality during the study.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The 96-hour LC50 was determined to be > 55.1 mg 2AE/L (arithmetic mean), and > 11.1 mg Pt/L (arithmetic mean).
- Executive summary:
A 96-h acute Danio rerio study was conducted for dihydrogen hexahydroxyplatinate, compound with 2-aminoethanol (1:2). The study is reliable without restrictions, being GLP-compliant and having followed standard test guidelines (OECD 203 and EU Method C.1).
A semi-static test system was used, where test solutions were renewed after 48 hours. Five test concentrations were used, and these were analysed separately for platinum and 2-aminoethanol (2AE) using acid digestion with ICP-OES and LC-MS/MS, respectively, at the start and at each renewal until the end of the test. The mean measured concentration of the freshly prepared highest test concentration was found to be 10.1 mg Pt/L, and 11.3 mg Pt/L for the aged test solution. The mean measured concentration of 2AE in the freshly prepared highest test concentration was found to be 54.8 mg/L for 2AE, which corresponded to 56.5 % of nominal. The mean measured concentration of the aged highest test solution was 55.5 mg/L for 2AE, corresponding to 57.3 % of nominal. All validity criteria were met.
The 96-hour LC50 was determined to be > 55.1 mg 2AE/L (arithmetic mean), and > 11.1 mg Pt/L (arithmetic mean).
Reference
Description of key information
The LC50 was determined to be >11.1 mg Pt L-1, or >55.1 mg 2-aminoethanol L-1.
Key value for chemical safety assessment
Additional information
An acute study is available with dihydrogen hexahydroxyplatinate, compound with 2-aminoethanol following OECD test guideline 203, with Danio rerio (Muth-Köhne 2016). Five nominal test concentrations were used, and the test was conducted under semi-static conditions with test media renewal at 48 hours. Analytical verification of test solutions at 0, 48 (aged and fresh solutions) and 96 hours was conducted and analysis of both platinum and 2-aminoethanol was carried out. Mean measured concentrations of 2-aminoethanol in fresh solutions ranged from 55.8 to 58.2% of nominal and in aged solutions ranged from 57.2 to 58.8% of nominal. Mean measured concentrations of platinum were approximately 7% of nominal for fresh and aged test solutions. The test item separated into the two components during the study therefore measured concentrations of the test item as a whole could not be determined. No mortality and no signs of stress or disease were observed in any of the test concentrations. The LC50 was therefore determined to be >11.1 mg Pt L-1, or >55.1 mg 2-aminoethanol L-1.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.