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EC number: 215-231-4 | CAS number: 1314-35-8
- 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
- Study period:
- November 4, 2002 - November 8, 2002
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Remarks:
- Well documented, scientifically sound study that was conducted in accordance with GLP and generally accepted guidelines
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- no data
- Vehicle:
- no
- Details on test solutions:
- no data
- Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- TEST ORGANISM
- Common name: Zebra fish
- Source: Di Mamma (Netherlands)
- Length at study initiation (length definition, mean, range and SD): mean 3.5 cm (S.D. = 0.33 cm)
ACCLIMATION
- Acclimation period: Stock held since September 2, 2002 and acclimatised to the test conditions since then.
- Acclimation conditions (same as test or not): same
- Type and amount of food: Commerical fish food
- Feeding frequency: daily; discontinued 24 hours prior to the test
- Health during acclimation (any mortality observed): < 5% mortalities - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- no data
- Hardness:
- 173.1 mg/L CaC03
- Test temperature:
- 20.8-22.0 °C (in the temperature range of 20-24 °C)
- pH:
- 7.5-7.7
- Dissolved oxygen:
- 8.2-8.4 mg/L (92-97% saturation)
- Salinity:
- n/a
- Nominal and measured concentrations:
- Nominal: 2.5 mg/L (WO3)
Measured: 5.2 - 5.3 mg/L (WO3)
Measured: 4.15 - 4.20 mg/L (W) - Details on test conditions:
- TEST SYSTEM
- Test vessels: Glass aquaria holding 5 L of test media
- Aeration: gentle aeration via narrow glass tubes
- Experimental design: 1 test concentration (2.5mg/L) plus 1 control, no feeding during the exposure period, static system
- Renewal rate of test solution (frequency/flow rate): None
- No. of organisms per vessel: 10 animals per test concentration
- Photoperiod: 16 hours light, 8 hours dark
- Biomass loading rate: 0.88 g body weight (wet weight) per litre
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Reconstituted water prepared according to the recommendations of ISO 7346. This freshly prepared standard dilution water is used for both the maintenance of the test animals under flow-through conditions and the preparation of stock and test solutions of the test substance. - Reference substance (positive control):
- no
- Duration:
- 48 h
- Dose descriptor:
- LC0
- Effect conc.:
- >= 5.25 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Remarks:
- WO3
- Basis for effect:
- mortality (fish)
- Duration:
- 48 h
- Dose descriptor:
- LC0
- Effect conc.:
- >= 4.16 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- act. ingr.
- Remarks:
- Tungsten (W)
- Basis for effect:
- mortality (fish)
- Duration:
- 72 h
- Dose descriptor:
- LC0
- Effect conc.:
- >= 5.26 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Remarks:
- WO3
- Basis for effect:
- mortality (fish)
- Duration:
- 72 h
- Dose descriptor:
- LC0
- Effect conc.:
- >= 4.18 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- act. ingr.
- Remarks:
- Tungsten (W)
- Basis for effect:
- mortality (fish)
- Duration:
- 96 h
- Dose descriptor:
- LC0
- Effect conc.:
- >= 5.25 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Remarks:
- WO3
- Basis for effect:
- mortality (fish)
- Duration:
- 96 h
- Dose descriptor:
- LC0
- Effect conc.:
- >= 4.16 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- act. ingr.
- Remarks:
- Tungsten (W)
- Basis for effect:
- mortality (fish)
- Details on results:
- All results are expressed in terms of mean measured concentrations. Measured concentrations correspond to 212% of nominal values of tungsten trioxide at 0 hours, to 208% of nominal values of tungsten trioxide at 24 hours, to 212% of nominal values of tungsten trioxide at 48 hours to 212% of tungsten trioxide at 72 hours, and 208% of nominal values of tungsten trioxide at 96 hours, respectively.
- Results with reference substance (positive control):
- n/a
- Reported statistics and error estimates:
- no data
- Conclusions:
- Highest test concentration resulting in 0% mortality (LC 0 96h): >= 5.25 mg/L test substance.
- Endpoint:
- short-term toxicity to fish
- Type of information:
- read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Study period:
- 2008-09-25 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 conducted in accordance to GLP and OECD guideline 203 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 similar or lower transformation/dissolution results for tungsten trioxide (the target substance) than sodium tungstate (the source substance), the resulting toxicity potential would also be expected to be similar or lower, so read-across is appropriate. In addition, read-across is justified because the classification and labeling is the same or less severe for the target substance PBT/vPvB profile is the same. Finally, the dose descriptors are, or are expected to be, sufficiently similar or higher for the target substance, 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 trioxide
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 203 (Fish, Acute Toxicity Test)
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 0 (control), 13, 25, 50, 100, and 200 mg/L; A volume of 10 mL was collected from each control and test substance replicate at 0 and 96 hours 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.
- 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: 7.5075 g of sodium tungstate dihydrate was added to a 21-L glass jar and bringing the jar to a volume of 15,000 mL with blended freshwater. Appropriate aliquots of the primary standard were diluted with 15 L of dilution water to prepare final test concentrations of 13, 25, 50, 100, and 200 mg total product/L. The control solution consisted only of dilution water. - Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- TEST ORGANISM
- Common name: Zebrafish
- Source: Osage Catfisheries, Osage Beach, Missouri
- Age at study initiation (mean and range, SD): Not specified
- Length at study termination (length definition, mean, range and SD): 28-31 mm; mean 30 ± 1.2 mm (Controls only)
- Weight at study termination (mean and range, SD): 0.194-0.408 g; mean 0.276 ± 0.0664 g (Controls only)
- Feeding during test
- Frequency: Not fed during test, or one day prior
ACCLIMATION
- Acclimation period: 5 days
- Acclimation conditions (same as test or not): Temperature adjusted for test
- Type and amount of food: Salmon starter, flake food, and brine shrimp
- Feeding frequency: Daily
- Health during acclimation (any mortality observed): No mortality observed in 14 days prior to testing. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Hardness:
- 140 mg/L CaCO3
- Test temperature:
- 23 ± 1 °C
- pH:
- 8.0-8.3 SU
- Dissolved oxygen:
- 6.7-8.3 mg/L (82 to 101% sat)
- Salinity:
- Not applicable
- Nominal and measured concentrations:
- Nominal- 0 (control), 13, 25, 50, 100, and 200 mg/L.
Mean calculated-- Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Type (delete if not applicable): closed
- Material, size, headspace, fill volume: 21 L glass jars, covered with plastic Petri dishes; 15 L test solution.
- Aeration: None
- No. of organisms per vessel: 10
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
- Biomass loading rate: 0.18 g fish tissue/L test solution
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Moderately hard freshwater made with naturally hard well water blended with well water demineralized by reverse osmosis, total hardness of 130-160 mg/L CaCO, passed through a sediment filter 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: 150 mg/L CaCO3
- Conductivity: 328 uS
- Intervals of water quality measurement: Daily
OTHER TEST CONDITIONS
- Adjustment of pH: None
- Photoperiod: 16h light/ 8h dark, with 30 min simulated dawn and dusk periods
- Light intensity: 542 lux at initiation of the definitive test as measured with a LI COR Model LI-189 light meter equipped with a photometric sensor.
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Mortality, 24h
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2x
- Range finding study: Other studies indicated a low potential for toxicity to aquatic organisms; Therefore, a range finding study was not performed. Definitive testing was performed at a level that exceeds the guideline-required maximum, 100 mg/L for this test.
- Reference substance (positive control):
- no
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 200 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: No mortality in any control or test solution
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 181 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Remarks:
- based on mean calculated concentrations of sodium tungstate
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: No mortality in any control or test solution
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 200 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Remarks on result:
- other: Lack of mortality and sublethal effects
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 181 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Remarks:
- based on mean calculated concentrations of sodium tungstate
- Basis for effect:
- behaviour
- Remarks on result:
- other: Lack of mortality and sublethal effects
- Details on results:
- Biological Results:
After 96 hours of exposure, there was no mortality in the 0 (control) or any of the test substance treatments. There were no sublethal observations during the exposure. The estimated 24-, 48-, 72-, and 96- hour LC50 values for zebrafish exposed to sodium tungstate dihydrate were >200 mg/L, the highest concentration tested. Since there was no partial response, the 96-hour slope of the concentrations-response line could not be calculated from the probit analysis. The 96 hour no-observed-effect concentration (NOEC) was 200 mg/L based on the lack of mortality and sublethal effects atthis and lower test substance concentrations.- Reported statistics and error estimates:
- 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 based on the absence of any mortality or sublethal effects.
- Conclusions:
- Based on nominal concentrations, the estimated 96 hour LC50 value for zebrafish exposed to sodium tungstate dihydrate was >200 mg/L, the highest concentration tested. The 96 hour slope of the concentrations-response line could not be calculated. The 96-hour no-observed-effect concentration (NOEC) was 200 mg/L, based on the lack of mortality and sublethal effects at this and the lower concentrations.
- Executive summary:
No fish short-term toxicity data of sufficient quality are available for tungsten trioxide (target substance). However, fish short-term 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 classification and labelling is more protective for the source substance than the target substance, the PBT/vPvB profile is the same, and the dose descriptors are, or are expected to be, lower for the source substance. For more details, refer to the read-across category approach description in the Category section of this IUCLID submission or Annex 3 of the CSR.
Referenceopen allclose all
Description of key information
No deaths were observed at saturation concentration under exposure conditions in an acute toxicity test with tungsten trioxide; therefore, a definitive LC50 could not be determined and read-across to sodium tungstate is used for this endpoint. In a flow-through test using zebrafish and testing another soluble tungsten compound with the same classification and PBT profile (sodium tungstate) the LC50 observed was found to be greater than the highest concentration tested (>181 mg sodium tungstate/L or approximately 106 mg W/L).
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 106 mg/L
Additional information
Due to similar or lower transformation/dissolution results for tungsten trioxide (the target substance) than sodium tungstate (the source substance), the resulting toxicity potential would also be expected to be similar or lower, so read-across is appropriate. In addition, read-across is justified because the classification and labeling is the same or less severe for the target substance PBT/vPvB profile is the same. Finally, the dose descriptors are, or are expected to be, sufficiently similar or higher for the target substance, and read-across to the source chemical is adequately protective. For more details, refer to the read-across category approach description in the Category section of this IUCLID submission or Annex 3 of 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.
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