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EC number: 241-602-5 | CAS number: 17625-03-5
- 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
Long-term toxicity to fish
Administrative data
- Endpoint:
- adult fish: sub(lethal) effects
- Data waiving:
- study scientifically not necessary / other information available
- Justification for data waiving:
- other:
Cross-reference
- Reason / purpose for cross-reference:
- data waiving: supporting information
Reference
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2020
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- Version / remarks:
- 30 May 2008
- Deviations:
- yes
- Remarks:
- On day 4 observations were performed only once. Because no mortality was ob-served after 96 hours, this was stated as uncritical.
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Version / remarks:
- Second edition, adopted 08. Feb. 2019.
- Deviations:
- yes
- Remarks:
- On day 4 observations were performed only once. Because no mortality was ob-served after 96 hours, this was stated as uncritical.
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- A stock solution containing 1000.3 mg/L in tap water was prepared. The concentration to be tested was prepared by diluting of this stock solution with tap water.
- Vehicle:
- yes
- Details on test solutions:
- A stock solution containing 1000.3 mg/L in tap water was prepared. The concentration to be tested was prepared by diluting of this stock solution with tap water.
Test Medium
Good quality drinking water is used. The composition is analysed yearly by the supplier. - Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- Specification
Species: Danio rerio HAMILTON-BUCHANAN
Age: sexually immature young fish, length 1-2 cm
Origin
The original animals are obtained in 2019 from the University Heidelberg and used for breeding and production of eggs. The offspring of the original animals is used in the test.
Husbandry
Danio rerio is routinely used for toxicity tests. The test fish are kept under following conditions:
Vessels: polyethylene aquaria
Medium: tap water
Feeding: three times a day with warmwater fishfood
Photo period: 12/12 hours, using neon tubes
Temperature: 23 +/- 2 °C - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Post exposure observation period:
- Observations were made after 1 h, 4 h and 24 h after the start of the exposure (day 0-1). On days 2-3 of the test, all vessels with were inspected twice per day (morning and afternoon). On day 4, the vessels were inspected only at the end of the experiment.
The content of the test item in the test vessels was measured at the beginning and at the end of the study. - Hardness:
- Blank control hardness in mg CaCO3/L = 106.8
Drinking water hardness = 0.88 mmol/L - Test temperature:
- 23 ± 2 °C
- pH:
- Blank control: 7.9 (0 h); 7.8 (24 h); 7.8 (48 h); 7.8 (72 h); 7.9 (96 h)
solution 100 mg/L: 7.2 (0 h); 7.7 (24 h); 7.8 (48 h); 7.8 (72 h); 7.9 (96 h) - Dissolved oxygen:
- Blank control [O2 in mg/L]: 8.9 (0 h); 8.2 (24 h); 6.8 (48 h); 7.4 (72 h); 7.1 (96 h)
solution 100 mg/L [O2 in mg/L]: 8.2 (0 h); 8.5 (24 h); 7.6 (48 h); 7.8 (72 h); 7.5 (96 h) - Salinity:
- sodium: 4.4 mg/L
potassium: 2.5 mg/L
calcium: 32 mg/L
magnesium: 2.1 mg/L
aluminium: 0.007 mg/L
iron: <0.005 mg/L
manganese: <0.005 mg/L
ammonium: <0.05 mg/L
nitrate: 1.4 mg/L
nitrite: <0.01 mg/L
chloride: 9.2 mg/L
sulphate: 10 mg/L - Conductivity:
- Conductivity of drinking water at 25 °C = 210 µS/cm
- Nominal and measured concentrations:
- At the start and at the end of the test, the content of the test item in the test solutions was determined using HPLC. The measured concentrations lay between 99 % and 109 % of the nominal concentrations. Therefore, the determination of the results was based on the nominal concentrations (see OECD Guidance Doc. No.23 (§176)).
- Details on test conditions:
- 24 hours before the start of the test, the test fish were no longer fed.
Date: 11. – 15. Nov. 2019
Treatment: 100 mg/L
Test Design: static
Medium renewal: none
Duration: 96 hours
Loading: 1 fish/L
Vessels: glass aquaria, maximal volume 12 L
Aeration: accomplished with glass tubes
Feeding: none
Photo period: 12/12 hours using neon tubes
Temperature: 23 ± 2 °C
pH adjustment: none
Replicate (Treatments): 1 vessel, each containing 7 L test solution and 7 fish
Replicate (Blank Control): 1 vessel, containing 7 L tap water and 7 fish
Observations were made after 1 h, 4 h and 24 h after the start of the exposure (day 0-1). On days 2-3 of the test, all vessels with were inspected twice per day (morning and afternoon). On day 4, the vessels were inspected only at the end of the experiment.
The content of the test item in the test vessels was measured at the beginning and at the end of the study. - Reference substance (positive control):
- no
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: the tested concentration showed no mortality.
- Details on results:
- Please see detials on results reported in section "any other information on results incl. tables".
- Results with reference substance (positive control):
- Positive control has not been used.
- Reported statistics and error estimates:
- The tested concentration showed no mortality. Therefore, no statistical evaluation of the biological results was performed and the LC50 is given as a range.
- Sublethal observations / clinical signs:
The mortalities were recorded daily and can be found in the following table.
Table. Mortality (1 h – 24 h)
Nominal Conc. in mg/L
Total number of fish used
Number of dead fish
1 h
4 h
24 h
Blank control
7
0
0
0
100
7
0
0
0
Table. Mortality (day 2 – 4)
Nominal Conc. in mg/L
Total number of fish used
Number of dead fish
2 d
3 d
4 d
morning
afternoon
morning
afternoon
Blank control
7
0
0
0
0
0
100
7
0
0
0
0
0
No mortality and no abnormal behaviour of the surviving fish was observed.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The tested concentration showed no mortality; therefore, 96h LC50 for fish is > 100 mg/L.
- Executive summary:
One valid experiment was performed.
The toxicity against Danio rerio was tested using a static test design according to OECD Guideline 203. The control and the tested concentration showed no mortality. No abnormal behaviour of the surviving fish was observed.
At the start and at the end of the test, the content of the test item in the test solutions was determined using HPLC. The measured concentrations lay between 99 % and 109 % of the nominal concentrations. Therefore, the determination of the results was based on the nominal concentrations (see OECD Guidance Doc. No.23 (§176)).
No observations were made which might cause doubts concerning the validity of the study outcome. All validity criteria were met.
The result of the test is considered valid.
Data source
Materials and methods
Results and discussion
Applicant's summary and conclusion
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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