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Diss Factsheets
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EC number: 231-143-9 | CAS number: 7440-33-7
- 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
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Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Study period:
- 2008-10-14 to: 2009-03-13
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- Well documented, scientifically sound study that was conducted in accordance to GLP and OECD guideline 202 with no deviation to the protocol. The reliability of this study for the substance tested is a K1, but in application of read-across to a different substance ECHA’s guidance specifies that the score can be a maximum of K2. Due to lower transformation/dissolution results for tungsten metal (the target substance) than sodium tungstate (the source substance), the resulting toxicity potential would also be expected to be lower, so read-across is appropriate. In addition, read-across is justified because the classification and labelling is the less severe for the target substance and the PBT/vPvB profile is the same. Finally, the dose descriptor for the target substance is expected to be sufficiently higher than the source chemical, and read-across to the source chemical is adequately protective. For more details refer to the attached description of the read across approach on Annex 3 in the CSR.
- Justification for type of information:
- 1. HYPOTHESIS FOR THE CATEGORY APPROACH: The hypothesis is that properties are likely to be similar or follow a similar pattern because of the presence of a common metal ion, in this case tungstate.
2. SOURCE AND TARGET CHEMICAL(S) (INCLUDING INFORMATION ON PURITY AND IMPURITIES):
Source: Sodium Tungstate
Target: Tungsten metal
3. CATEGORY APPROACH JUSTIFICATION: See Annex 3 in CSR
4. DATA MATRIX: See Annex 3 in CSR - Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material (migrated information):
no data - Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 10 mL from each control and treatment at 0 and 48 h and transferred to a culture tube.
- Sampling method: 0.05 mL aliquot of each sample was taken, diluted if necessary with 2% HNO3, capped and shaken to mix and analyzed by ICP MS.
- Sample storage conditions before analysis: Room temperature - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: 0.4004 g sodium tungstate dihydrate was dissolved in 2 L aged-blended freshwater. Test concentrations were diluted from this solution.
- Controls: Aged-blended freshwater only.
- Evidence of undissolved material (eg precipitate, surface film, etc): None - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Water flea
- Source: In-house daphnid culture
- Age at study initiation (mean and range, SD): <24h
- Feeding during test
- Frequency: Not fed during test
ACCLIMATION
- Acclimation period: None necessary, as culture conditions are the same as test conditions
- Type and amount of food: Suspension of Pseudokirchneriella subcapitata, suplemented by artificial diet.
- Feeding frequency: Daily
- Health during acclimation (any mortality observed): No mortality in adults at least 48 h prior to testing
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- None
- Hardness:
- 144 mg/L CaCO3
- Test temperature:
- 19.3-19.5 °C
- pH:
- 8.3-8.5 SU
- Dissolved oxygen:
- 7.6-7.9 mg/L (85 to 89% saturation)
- Salinity:
- n/a
- Nominal and measured concentrations:
- Nominal- 0, 13, 25, 50, 100 and 200 mg/L
Mean Calculated- < MQL, 11.9, 21.5, 41.5, 90.8, and 163 mg/L - Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Type (delete if not applicable): closed
- Material, size, headspace, fill volume: Glass 250 mL jars, containing 200 mL test solution, covered with a plastic Petri dish
- Aeration: No
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: ABC well water mixed with well water demineralized by reverse osmosis, then aged in a tank containing aquaticorganisms. Water was then passed through a sediment filter, a UV sterilizer, and aerated prior to use.
- Metals: B-0.415 mg/L, Ca-83.1 mg/L, Mg- 33.1 mg/L, K-7.93 mg/L, Na-32.2 mg/L; all others below DL.
- Pesticides: Below DL
- Alkalinity: 142 mg/L CaCO3
- Conductivity:347 uS
- Culture medium different from test medium: No
- Intervals of water quality measurement: Daily
OTHER TEST CONDITIONS
- Adjustment of pH: No
- Photoperiod: 16 hr light, 8hr dark
- Light intensity: 448 lux as measured with a LI-COR Model LI-189 light meter equipped with a photometric sensor.
- The jars were maintained at 20 ± 2 °C in a temperature-controlled water bath.
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Immobility and mortality, 24 hr.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2x
- Range finding study
- Test concentrations: 0, 0.10, 1.0, 10, and 100 mg/L
- Results used to determine the conditions for the definitive study: Yes - Reference substance (positive control):
- no
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 163 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- other: sodium tungstate concentration
- Basis for effect:
- other: immobilization
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 163 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- other: sodium tungstate concentration
- Basis for effect:
- other: immobilization
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 90.8 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- other: sodium tungstate concentration
- Basis for effect:
- other: immobilization
- Details on results:
- Biological Results:
After 48 hours of exposure, immobility was 0, 0, 0, 0, 5 and 15% in the163 mg /L, the highest level tested. Immobility was significantly increased at only the highest test concnetration level. The 48-hour no-observed-effect concentration (NOEC) was determined to be 90.8 mg/L, based on the lack of statistically significant (p=0.05) immobility and sublethal effects at this test substance treatment. - Results with reference substance (positive control):
- n/a
- Reported statistics and error estimates:
- All statistical analyses were performed with SAS software. Estimates of LC50 values and their 95% confidence limits were calculated using the probit method and Trimmed Spearman-Karber method. When the p value for Goodness of Fit was >0.05 and there was no other evidence of questionable convergence, the probit method was selected for reporting. When this criterion was not achieved, the Trimmed Spearman-Karber method was selected for reporting. The no-observed-effect concentration (NOEC) was determined by using a one-tailed Dunnett’s test.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The 48 hour EC50 value was estimated to be >163 mg/L. The 48-hour no-observed-effect concentration (NOEC) was 90.8 mg/L based on the lack of statistically significant (p=0.05) immobility and sublethal effects at this and lower test substance treatments.
- Executive summary:
No aquatic invertebrates acute toxicity data of sufficient quality are available for tungsten metal (target substance). However, aquatic invertebrates acute toxicity data are available for sodium tungstate (source substance), which are used for read-across. Due to lower water solubility and lower toxicity for the target substance compared to the source substance, the resulting read-across from the source substance to the target substance is appropriate as a conservative estimate of potential toxicity for this endpoint. In addition, read-across is appropriate because the PBT/vPvB profile is the same, and the dose descriptors are, or are expected to be, higher for the source substance. For more details, refer to the read-across category approach in the Category section of this IUCLID submission or Annex 3 in the CSR.
Reference
Description of key information
No data were available for tungsten metal for short-term invertebrate toxicity; therefore, read-across to sodium tungstate was used for this endpoint. In a test using Daphnia and testing sodium tungstate, the EC50 observed was found to be greater than the highest concentration tested (>163 mg sodium tungstate/L or >96 mg W/L).
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 96 mg/L
Additional information
Due to lower transformation/dissolution results for tungsten metal (the target substance) than sodium tungstate (the source substance), the resulting toxicity potential would also be expected to be lower, so read-across is appropriate. In addition, read-across is justified because the classification and labelling is the less severe for the target substance and the PBT/vPvB profile is the same. Finally, the dose descriptor for the target substance is expected to be sufficiently higher than the source chemical, and read-across to the source chemical is adequately protective. For more details, refer to the read-across category approach in the Category section or Annex 3 in the CSR.
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.
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