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EC number: 848-535-6 | CAS number: 2267262-12-2
- 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:
- 2020-06-02 to 2020-06-06
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Version / remarks:
- adopted 18 June 2019
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- Version / remarks:
- 440/2008/EC, 30 May 2008
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 850.1075 (Freshwater and Saltwater Fish Acute Toxicity Test)
- Version / remarks:
- October 2016
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- - Sampling method: For determination of the test item concentrations, five replicate samples were taken from the test solution (5×3 mL) and five replicate samples from the control solution (5×3 mL) at the start and at the end of the test. The sampling was performed from different part of the aquariums.
- Sample storage conditions before analysis: no - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: The test solution used in the test was prepared by mechanical dispersion without using of any solubilising agent. An amount of 0.5015 g test item was dissolved in 5015 mL dilution water (ISO medium) in order to obtain the nominal concentration of 100 mg/L.
- Controls: negative control
- Evidence of undissolved material: no - Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- TEST ORGANISM
- Common name: zebrafish
- Source: Akvárium Magazin Kft. (Pasaréti Gyula), 1222 Budapest, Dévény u. 36., Hungary
- Age at study initiation (mean and range, SD): juveniles
- Length at study initiation: total length 1-2 cm
- Weight at study initiation: 0.07 g (calculated mean of 1 fish)
ACCLIMATION
- Acclimation period: at least 9 days before test initiation
- Acclimation conditions:
Fish were held for in the fish laboratory under the following conditions:
Water: ISO medium (same as used for the test)
Photoperiod: 12 to 16 hours light daily
Temperature: 21 – 25°C
Oxygen concentration: at least 80 % of air saturation
- Type and amount of food during acclimation:
- Feeding frequency during acclimation: three times per week or daily until 24 – 48 hours before the test is started
- Health during acclimation: fish were apparently healthy and no mortality was observed
FEEDING DURING TEST
- Food type: no - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- None
- Hardness:
- The reconstituted water (ISO medium) has an approximate theoretical total hardness of 249 mg/L (as CaCO3).
- Test temperature:
- 22.4 – 22.8 °C
- pH:
- 7.67 – 9.41
- Dissolved oxygen:
- 81.3 – 90.9 % of air saturation
- Salinity:
- not applicable
- Conductivity:
- not specified
- Nominal and measured concentrations:
- nominal: 100 mg/L
measured (after 96 hours): 98.2 mg/L (arith. mean) - Details on test conditions:
- TEST SYSTEM
- Test vessel: aquaria
- Type: open
- Material, fill volume: glass, fill volume = 5 L
- Aeration: no
- No. of organisms per vessel: 10
- No. of vessels per concentration: 1
- No. of vessels per control: 1
- Biomass loading rate: 0.15 g/L in the control and 0.13 g/L in the test item treated group
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: ISO Medium prepared using deionised water (prepared in TOXI-COOP ZRT. by BWT Christ Ministil water purification system)
OTHER TEST CONDITIONS
- Adjustment of pH: no
- Photoperiod: 16 h light : 8 h dark
- Light intensity: 639 lux
EFFECT PARAMETERS MEASURED: Fish were observed at approximately 2, 6, 24, 48, 72 and 96 hours after start of the test for signs of intoxication and mortality.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: not applicable (limit test)
- Justification for using less concentrations than requested by guideline: Based on the results of a preliminary test, no toxicity of the test item was expected on Zebrafish up to 100 mg/L (limit concentration). Therefore a limit test was performed using only this concentration level and a control in order to demonstrate that the test item is not toxic to Zebrafish up to at least the limit concentration of 100 mg/L.
- Test concentrations: 100 mg/L
- Results used to determine the conditions for the definitive study: yes - Reference substance (positive control):
- not required
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Duration:
- 96 h
- Dose descriptor:
- LOEC
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Details on results:
- - Behavioural abnormalities: not observed
- Observations on body length and weight: no
- Other biological observations: no
- Mortality of control: no
- Other adverse effects control: no
- Abnormal responses: no
- Any observations that might cause a difference between measured and nominal values: no
- Effect concentrations exceeding solubility of substance in test medium: no - Results with reference substance (positive control):
- not applicable
- Reported statistics and error estimates:
- Since a limit test was performed (and mortality did not occur), no statistical analysis was necessary. Endpoints were determined directly from the raw data.
- Sublethal observations / clinical signs:
Table 1: Cumulative Mortality Data
Test Group
Cumulative mortality
(initial population = 10 fish / test group)2h
6h
24h
48h
72h
96h
Control
0
0
0
0
0
0
100 mg/L
0
0
0
0
0
0
Table 2: Measured and calculated Data of Body Weight
Test Group
Measured weight
of 10 fish (g)Calculated mean
weight of 1 fish (g)Loading of testing aquarium
(g fish/L testing liquid)Control
0.77
0.08
0.15
100 mg/L
0.65
0.07
0.13
Table 3: Body Length of Test Animals
Test Group
Body length [cm]
Control
1.80
1.90
2.00
1.85
1.85
1.90
1.75
1.95
1.80
1.90
100 mg/L
1.70
1.85
2.00
1.95
1.90
2.00
1.75
1.80
1.90
1.85
Table 4: pH-values measured during the Experiment
Test Group
pH
0h
24h
48h
72h
96h
Control
7.89
7.82
7.67
7.91
7.91
100 mg/L
9.41
8.90
8.58
8.45
8.17
Table 5: Dissolved Oxygen Concentrations measured during the Experiment
Test Group
Dissolved Oxygen Concentration [%]
0h
24h
48h
72h
96h
Control
89.5
84.5
83.2
82.9
81.3
100 mg/L
90.9
89.0
88.2
87.4
87.0
Table 6: Temperatures measured during the Experiment
Test Group
Temperature[°C]
0h
24h
48h
72h
96h
Control
22.4
22.7
22.8
22.7
22.6
100 mg/L
22.6
22.8
22.8
22.7
22.7
Table 7: Concentration of Test Item measured in the Test Solutions
Nominal concentration mg/L
Measured concentrations
Start(June 02, 2020)
End(June 06, 2020)
Concentration (mg/L)
% of the nominal
Concentration (mg/L)
% of the nominal
Control
not detected
-
not detected
-
100
83.41
83
99.49
99
100.80
101
96.80
97
102.58
103
99.35
99
101.09
101
98.05
98
101.26
101
97.62
98
- Validity criteria fulfilled:
- yes
- Conclusions:
- In a static acute toxicity test according to OECD TG 203 with Danio rerio the 96-hour LC50 of the test item was determined to be >100 mg/L (nominal).
- Executive summary:
To evaluate the acute toxicity of the test item on Zebrafish (Danio rerio) a static 96-hour test according to OECD TG 203, EU Method C.1. and US EPA OCSPP 850.1075 was carried out in compliance with the GLP principles. Based on the results of a preliminary study 10 animals were exposed to a single limit concentration of 100 mg/L (nominal). A negative control with ISO Medium but without the test item was performed in parallel. The test item concentration was analytically verfied by using HPLC-UV and found to be 83 –103 % of the nominal at the start, and 97 – 99 % of the nominal at the end of the test. Therefore, all biological results are based on nominal concentrations. Fish were observed at approximately 2, 6, 24, 48, 72 and 96 hours after start of the test for signs of intoxication and mortality. All validity criteria of the test guidelines were fulfilled. As a result, no toxic effect on fish was observed at the limit concentration of 100 mg/L. Accordingly, the 96-hour LC50 value was determined to be > 100 mg/L. The 96-hour NOEC was determined to be 100 mg/L.
Reference
Description of key information
In a static acute toxicity test according to OECD TG 203 with Danio rerio the 96-hour LC50 of the test item was determined to be >100 mg/L (nominal).
Key value for chemical safety assessment
Additional information
To evaluate the acute toxicity of the test item on Zebrafish (Danio rerio) a static 96-hour test according to OECD TG 203, EU Method C.1. and US EPA OCSPP 850.1075 was carried out in compliance with the GLP principles. Based on the results of a preliminary study 10 animals were exposed to a single limit concentration of 100 mg/L (nominal). A negative control with ISO Medium but without the test item was performed in parallel. The test item concentration was analytically verfied by using HPLC-UV and found to be 83 –103 % of the nominal at the start, and 97 – 99 % of the nominal at the end of the test. Therefore, all biological results are based on nominal concentrations. Fish were observed at approximately 2, 6, 24, 48, 72 and 96 hours after start of the test for signs of intoxication and mortality. All validity criteria of the test guidelines were fulfilled. As a result, no toxic effect on fish was observed at the limit concentration of 100 mg/L. Accordingly, the 96-hour LC50 value was determined to be > 100 mg/L. The 96-hour NOEC was determined to be 100 mg/L.
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