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EC number: 947-581-5 | CAS number: 2209852-19-5
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- Endpoint summary
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- Environmental data
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- 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
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- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
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- Specific investigations
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- 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:
- 21-11-2018 to 13-03-2019
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study performed under GLP. All relevant validity criteria were met.
- Justification for type of information:
- Information as to the availability of the in vivo study is provided in 'attached justification'.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: Guidelines for the Testing of Chemicals, Effects on Biotic Systems, Version 2, 203 Fish Acute Toxicity Test, China Environmental Press, China (2013)
- Deviations:
- no
- Principles of method if other than guideline:
- The test was generally conducted in accordance with or equivalent to the following: China HJ/T153 - 2004 Chemical Test Guideline stipulations and Chemical Registration Center of MEP. The Guidelines for the Testing of Chemicals, effects on Biotic Systems, 203 Fish Acute toxicity test [M]. Second Edition. Beijing: China Environmental Press. 2013: 30-36. The test was also completed under OECD TG 203: Fish Acute Toxicity Test (1992).
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 0 (control), 5.00, 6.35, 8.06, 10.2, 13.0 and 16.5 mg/L nominal concentrations with geometric series factor 1.270 ; nominal concentrations were analytically confirmed to be maintained between 80 and 120% within the exposure period.
- Sampling method: 50 mL extract from test solution.
- Sample storage conditions before analysis: 50mL test solution were extracted three times with ethyl acetate (15 mL per extraction). Extracts were collected into 50 mL volumetric flasks and made up to volume with ethyl acetate. Then filtered through a 0.45 µm nylon filter membrane. With discarding of the first 5 to 10 mL filtrate. The samples were analysed immediately, otherwise the sample were pretreated as above and stored at 2°C to 8°C, protected from light within 96 hours. - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: 1.02 g test item was weighed into a flask and dissolved with test water, transferred into a 10 L - conical flask and diluted with test water to 10000 mL. After being sealed the test suspension was stirred on a magnetic stirrer for about 3 h (the depth of vortex was maintained at one third of the test solution height). Then test suspension was placed on magnetic stirrer for continuous mixing (the depth of vortex was maintained at one third of the test solution height). After stirring for 3 h, the nominal concentration of 10 mg/L was obtained. 491 mL, 623 mL, 791 mL, 1004 mL, 1275 mL and 1619 mL test stock solution were measured into 10 L vessels, 9510 mL, 9377 mL, 9209 mL, 8996 mL, 8725 mL and 8381 mL dechlorinated tap water were added respectively to obtain the concentrations of 5.00, 6.35, 8.06, 10.2, 13.0 and 16.5 mg/L.
- Eluate: Not applicable.
- Differential loading: Not applicable.
- Controls: A negative/blank control without test item or reference item was also included. A previously conducted sensitivity test with potassium dichromate (positive control/reference item) was performed. Full information provided in the full study report.
- Chemical name of vehicle (organic solvent, emulsifier or dispersant): Not applicable.
- Concentration of vehicle in test medium (stock solution and final test solution(s) or suspension(s) including control(s)): Not applicable.
- Evidence of undissolved material (e.g. precipitate, surface film, etc.): In the definitive test there was no evidence of undissolved test item. - Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- TEST ORGANISM
- Common name: Zebra fish (Brachydanio rerio)
- Strain: Not reported. Batch generation number FDr20180815-2
- Source: Recognised supplier (recorded in full study report) located in China.
- Age at study initiation (mean and range, SD): Not reported.
- Length at study initiation (length definition, mean, range and SD): Not reported. The body weight and total length of test fish in blank control were measured when the test was finished. The average and deviation of test fish total length and body weight were respectively 22.00 – 24.10 mm (mean = 23.01 +/- 1.86 mm ; meeting the requirement of 20.0±10.0 mm according to guideline) and 0.068 – 0.096 g (mean = 0.088 +/- 0.018 g). In the treated/control groups the loading was 0.062 g/L (i.e. < 1.0g fish/litre).
- Method of breeding: Not reported.
- Feeding during test: No.
- Food type: Feeding was conducted during acclimation (daily) until 24-hours prior to test initiation.
- Amount: No feeding during exposure. Not applicable.
- Frequency: No feeding during exposure. Not applicable.
ACCLIMATION
- Acclimation period: 40 days (i.e. > 48 hours)
- Acclimation conditions (same as test or not): Yes. Same water quality, temperature 23 ± 2°C and photoperiod as used during the test (14 hours light; 10 hours dark). Oxygen concentration was in the range of the exposure duration (> 80% air saturation).
- Type and amount of food: Not reported.
- Feeding frequency: Daily; until 24 hours before the start of the test.
- Health during acclimation (any mortality observed): None reported (0% during 7 days pre-test).
FEEDING DURING TEST
- Food type: Not applicable.
- Amount: Not applicable.
- Frequency: Not applicable. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Hardness:
- 145 mg/L expressed as CaCO3; Test water (dechlorinated water)
- Test temperature:
- Temperature 21.3 - 23.0 °C during test period, the test was performed in a temperature controlled environment with continuous monitoring and was maintained at 23 ± 2°C.
- pH:
- Test water (dechlorinated water): pH 6.0 - 8.5 (actual: pH 8.10) as specified in China Guidelines for the testing of Chemicals (2nd Ed.) 203 test.
The pH was in the range of 7.62-8.05 during the study. - Dissolved oxygen:
- The test solutions were not aerated during the exposure. The dissolved oxygen concentration in the test solutions during the test was kept at not less than 60 % of the air saturation value. Measured range: 92 to 104% ASV during the definitive test.
- Nominal and measured concentrations:
- - Preliminary range-finding test performed on static test system:
0 (control), 3.05, 31.2 and 100 mg/L nominal concentrations (open vessel)
The actual concentrations of test item in 3.05 mg/L and 9.77 mg/L test groups were measured by GC at 0 h, 24 h, 48 h and 96 h in the range-finding test.
Subsequently, a followup range-finder at 10 mg/L was completed (limited headspace and closed vessel) showed that 80 – 120% nominal concentrations were maintained.
- Definitive: 0 (control), 5.00, 6.35, 8.06, 10.2, 13.0 and 16.5 mg/L nominal concentrations (geometric series factor 1.270) ; nominal concentrations were analytically confirmed to be maintained between 80 and 120% within the exposure period. - Details on test conditions:
- TEST SYSTEM
- Test vessel: 10 L necked flask sealed with glass lid
- Type (delete if not applicable): closed
- Material, size, headspace, fill volume: glass. ca. 9000 mL fill volume (minimum headspace ca. 1500 mL)
- Aeration: Not continuously aerated although DOC > 60% ASV during exposure.
- Type of flow-through (e.g. peristaltic or proportional diluter): Not applicable.
- Renewal rate of test solution (frequency/flow rate): Not applicable (static system)
- No. of organisms per vessel: Seven (7) per vessel
- No. of vessels per concentration (replicates): None.
- No. of vessels per control (replicates): One (1)
- No. of vessels per vehicle control (replicates): Not applicable.
- Biomass loading rate: < 1.0 g/L (Actual: 0.062 g/L)
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Water used in the test was dechlorinated tap water (water quality analysis is indicated in the full study report).
- Conductivity: Not reported. Typically, would be: Water: 500±100μs/cm) as specified in China Water quality standard for fisheries in GB-11607-89.
- Culture medium different from test medium: No.
- Intervals of water quality measurement: Every 24 hour intervals; before and after renewal
OTHER TEST CONDITIONS
- Adjustment of pH: None.
- Photoperiod: 14 hours photoperiod daily
- Light intensity: Not reported.
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Mortalities and abnormalities; measured at 3h, 24h, 48h, 72h and 96h as applicable.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 1.270
- Justification for using less concentrations than requested by guideline: Not applicable. Five concentrations used.
- Range finding study: 0 (control), 3.05, 31.2 and 100 mg/L nominal concentrations (open vessel)
The actual concentrations of test item in 3.05 mg/L and 9.77 mg/L test groups were measured by GC at 0 h, 24 h, 48 h and 96 h in the range-finding test.
Subsequently, a followup range-finder at 10 mg/L was completed (limited headspace and closed vessel) showed that 80 – 120% nominal concentrations were maintained.
- Test concentrations: The cumulative mortalities of test fish in blank control and 3.05, 31.2 and 100 mg/L nominal concentrations (open vessel) test groups were 0%, 0%, 0%, 0% and 100%, respectively. The followup range-finder at 10 mg/L was completed (limited headspace and closed vessel) and indicated 71% cumulative mortality.
- Results used to determine the conditions for the definitive study: Yes. - Reference substance (positive control):
- yes
- Remarks:
- Potassium Dichromate
- Duration:
- 96 h
- Dose descriptor:
- LC0
- Effect conc.:
- 8.06 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: analytically confirmed nominal concentrations
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 10.4 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: C.I. 9.51 - 11.4 mg/L ; analytically confirmed nominal concentrations
- Duration:
- 96 h
- Dose descriptor:
- LC100
- Effect conc.:
- 13 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: analytically confirmed nominal concentrations
- Details on results:
- - Behavioural abnormalities: There were no abnormal responses of test fish in the blank control. Observed abnormal responses are reported in table 3.
- Observations on body length and weight: The body weight and total length of test fish in blank control were measured when the test was finished. The average and deviation of test fish total length and body weight were respectively 22.00 – 24.10 mm (mean = 23.01 +/- 1.86 mm ; meeting the requirement of 20.0±10.0 mm according to guideline) and 0.068 – 0.096 g (mean = 0.088 +/- 0.018 g).
- Mortality of control: None.
- Other adverse effects control: Yes. None reported.
- Abnormal responses: Observed abnormal responses are reported in table 3.
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: Not applicable.
- Effect concentrations exceeding solubility of substance in test medium: Not applicable. - Results with reference substance (positive control):
- - Results with reference substance valid? Yes
- 24h LC50: 250 (C.I. 214 - 291) mg/L - Reported statistics and error estimates:
- The LC50 values and the 95% confidence limits (LC5) at 24h after the start of the test were calculated by Probit Analysis software (US EPA: Probit Analysis Program Version 1.5). The LC50 value and the 95% confidence limits (L95) at 48h, 72h and 96h were calculated by Spearman-Karber software (US EPA: Trimmed Spearman-Karber Program Version 1.5).
- Sublethal observations / clinical signs:
Table 1. Median Lethal Concentration (LC50) and 95% confidence limits
Recommended observation times
LC50 (mg/L) based on analytically confirmed nominal concentrations
95% confidence limits (mg/L)
96 h
10.4
9.51 - 11.4
#1: LC50 based on geometric mean measured concentrations
Table 2. Cumulative mortality
Cumulative mortality #2
Nominal Concentration #1
Exposure duration (h)
3
24
48
72
96
Control
0.00 mg/L
0.0%
0.0%
0.0%
0.0%
0.0%
5.00 mg/L
0.0%
0.0%
0.0%
0.0%
0.0%
6.35 mg/L
0.0%
0.0%
0.0%
0.0%
0.0%
8.06 mg/L
0.0%
0.0%
0.0%
0.0%
0.0%
10.2 mg/L
0.0%
43.0%
43.0%
43.0%
43.0%
13.0 mg/L
0.0%
71.0%
100.0%
100.0%
100.0%
16.5 mg/L
100.0%
100.0%
100.0%
100.0%
100.0%
#1: nominal concentrations that were analytically confirmed
#2: n = 7 per concentration
Table 3. Observed abnormal responses
Visible abnormalities
Nominal Concentration #1
Exposure duration (h)
3
24
48
72
96
Control
0.00 mg/L
0/7
N
0/7
N
0/7
N
0/7
N
0/7
N
5.00 mg/L
0/7
N
3/7
IMM(3)
5/7
IMM(5)
4/7
AS(1)
IMM(3)
7/7
AS(2)
IMM(5)
6.35 mg/L
0/7
N
7/7
RA(4)
IMM(3)7/7
RA(2)
IMM(5)
7/7
RA(6)
IMM(1)
7/7
AS(2)
IMM(5)
8.06 mg/L
7/7
RA(7)
7/7
IMM(7)
7/7
IMM(5)
OLE(2)
7/7
IMM(4)
OLE(3)
7/7
IMM(6)
OLE(1)
10.2 mg/L
7/7
OLE(4)
RA(3)
4/4
IMM(3)
OLE(1)4/4
IMM(1)
OLE(3)
4/4
IMM(1)
OLE(3)
4/4
OLE(4)
13.0 mg/L
7/7
OLE(7)
2/2
LB(2)
-
-
-
-
-
-
16.5 mg/L
-
-
-
-
-
-
-
-
-
-
Note:
N : normal
IMM : immobilized at the bottom
AS : swimming at the surface
OLE : overturn and loss of balance equilibrium
LB : lying at the bottom
RA : reduction of activity
- : complete mortality
- Validity criteria fulfilled:
- yes
- Conclusions:
- The 96 hour LC50 for the test item to Danio rerio was determined to be 10.4 (C.I. 9.5 - 11.4) mg/L based on analytically confirmed nominal concentrations.
- Executive summary:
The acute toxicity of the test item to Zebra fish (Danio rerio) was determined in a 96 hour static test according to OECD TG 203 and the China Guidelines for the Testing of Chemicals, Effects on Biotic Systems, Version 2, 203 Fish Acute Toxicity Test (2013) under GLP. Based on the results of range finding tests the nominal concentrations of:0 (control), 5.00, 6.35, 8.06, 10.2, 13.0 and 16.5 mg/L nominal concentrations (geometric series factor 1.270)were selected for exposure to fish groups of 7 individuals.Nominal concentrations were analytically confirmed to be maintained between 80 and 120% within the exposure period by GC-FID.On this basis effect levels were indicated based on nominal concentrations. Observations were made at 3, 24, 48, 72 and 96 hours after the start of the exposure. During the definitive test the water temperature was in the 21.3 - 23.0 °C, pH was 7.62 to 8.05 and air saturation was 92 to 104% ASV indicating that environmental conditions were adequately maintained. Behavioural abnormalities and biological effects were reported during the course of the study. No abnormalities were observed in the control group. All validity criteria were considered to be met. The 96h median LC50 was 10.4 (C.I. 9.5 - 11.4) mg/L based on analytically confirmed nominal concentrations.
Reference
Description of key information
LC50 (fish) = 10.4 (C.I. 9.5 -11.4 ) mg/L based on analytically confirmed nominal concentrations, 96-hour, freshwater, OECD TG 203, 2019
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 10.4 mg/L
Additional information
Key study : OECD TG 203, 2019 : The acute toxicity of the test item to Zebra fish (Danio rerio) was determined in a 96 hour static test according to OECD TG 203 and the China Guidelines for the Testing of Chemicals, Effects on Biotic Systems, Version 2, 203 Fish Acute Toxicity Test (2013) under GLP. Based on the results of range finding tests the nominal concentrations of:0 (control), 5.00, 6.35, 8.06, 10.2, 13.0 and 16.5 mg/L nominal concentrations (geometric series factor 1.270)were selected for exposure to fish groups of 7 individuals.Nominal concentrations were analytically confirmed to be maintained between 80 and 120% within the exposure period by GC-FID.On this basis effect levels were indicated based on nominal concentrations. Observations were made at 3, 24, 48, 72 and 96 hours after the start of the exposure. During the definitive test the water temperature was in the 21.3 - 23.0 °C, pH was 7.62 to 8.05 and air saturation was 92 to 104% ASV indicating that environmental conditions were adequately maintained. Behavioural abnormalities and biological effects were reported during the course of the study. No abnormalities were observed in the control group. All validity criteria were considered to be met. The 96h median LC50 was 10.4 (C.I. 9.5 - 11.4) mg/L based on analytically confirmed nominal concentrations.
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