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EC number: 470-780-9 | CAS number: 55312-97-5
- 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
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:
- 31 Jul - 15 Dec 2006
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Version / remarks:
- 1992
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- Analytical Procedure - Standard Solutions used for Calibration
20.5 mg of the test item were dissolved in Acetonitrile and made up with Acetonitrile to the mark in a 100 mL volumetric flask to prepare a stock solution of 205 mg/L.
Defined volumes of this stock solution were diluted with Milliporewater to obtain standard solutions in the range of 0.041 to 4.10 mg/L.
Although the overall method sensitivity may be better, the concentration of the lowest used calibration solution is employed as the limit of quantification.
These solutions were used to calibrate the HPLC-system. - Vehicle:
- no
- Details on test solutions:
- To produce the only test concentration 501.6 mg of the test item were added to 5 litres of dilution water, then treated in an ultrasonic bath for 60 minutes and afterwards stirred for 24 hours on a magnetic stirrer. Finally undissolved particles of the test item were removed by filtration using a folded filter of pore size 7-12 µm.
- Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- Name: Zebra fish
Source: Aqua KlöGer (Germany)
Date supplied: 2006-10-24
Acclimatisation: Stock held since 2006-10-24 and acclimatised to the test conditions since then.
Temperature: 20 - 24 °C
Dissolved oxygen: > 5 mg/L
Feeding: Commercial fish food, daily. Discontinued 24 h prior to test.
Mortalities during acclimatisation period: < 5 %
Medication: none
Mean standard length (n = 20): 3.6 cm (S.D. = 0.21 cm) - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Test temperature:
- 21.5 - 22.4 °C
- pH:
- 7.7-7.8
- Dissolved oxygen:
- 8.7 - 9.0 mg/L
- Nominal and measured concentrations:
- nominal: 100 mg/L
measured: 84.3 mg/L (0 h) and 85.4 mg/L (96 h) - Details on test conditions:
- Test vessels: glass aquaria holding 5 L of test media
Experimental design: 1 test concentration plus 1 control10 animals per test concentration no feeding during the exposure period static system
Method of initiation: animals were placed in prepared media
Loading: 0.75 g body weight (wet weight) per litre
Photoperiod: 16 h light: 8 h dark
Temperature: mean +/- 1 °C (in the temperature range 20 - 24 °C)
Aeration: gentle aeration via narrow glass tubes
Test item concentration: 100 mg/L
Method of administration: direct weighing
Medium renewal: none
Duration of exposure: 96 hours
Criteria of effects: The criterion of death used in this study was the absence of response to physical stimulation. In addition to observations on mortality at 2, 24, 48, 72and 96 hours, subjective assessments were made on the type and incidence of sub-lethal effects compared with control fish. - Reference substance (positive control):
- no
- 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)
- Details on results:
- No toxic effects against fish were observed at a test concentration of 100 mg/L under static test conditions. All results are expressed in terms of nominal concentrations. Recovery rates corresponds to 84.3 % of nominal value at 0 hours and to 85.4 % of nominal value at 96 hours, respectively.
- Sublethal observations / clinical signs:
Validity criteria for the measurement of the short-term toxicity to fish:
Target condition according to guideline: Actual condition according to the study: Validity criteria met: In the control(s) (dilution water control, solvent control), the mortality should not exceed 10% (or one fish, if fewer than 10 control fish are tested) at the end of the exposure. Mortaility of zebra fish in the control was 0 after 96h. Yes The dissolved oxygen concentration should be ≥60 % of the air saturation value in all test vessels throughout the exposure Oxygen saturation ranged beween 96 - 101 % in the tests. Yes All fish should be held in the laboratory for at least 9 days before they are used for testing. The first 48 hours constitute a settling-in period. Then, fish should be acclimatised for at least 7 days (48 hours settling-in + 7 days acclimatisation = 9 days) in water similar to test water immediately before the start of the test. Stock held since Oct. 24, 2006 and acclimatised to the test conditions since then. Test was performed 31 Jul - 15 Dec 2006. Yes During the acclimatisation period, mortalities are recorded, and the following
criteria are applied:
- mortalities of greater than 10% of the population in seven days: reject the entire
batch;
- mortalities between 5 and 10% of the population: acclimatisation is continued
for seven additional days; and if there is more than 5% mortality during the
second seven day period, reject the entire batch;
- mortalities of less than 5% of population in seven days: accept the batch.Mortalities during acclimatisation period: < 5 % Yes Duration: 96 hours. Duration was 96 h. Yes The water temperature should not differ by more than 2 °C. Test temperature was: 21.5 - 22.4 °C. Yes - Validity criteria fulfilled:
- yes
- Remarks:
- See 'Any other information on results incl. tables'.
- Conclusions:
- No toxic effects against fish were observed at a test concentration of 100 mg/L under static test conditions. All results are expressed in terms of nominal concentrations. Recovery rates corresponds to 84.3 % of nominal value at 0 hours and to 85.4 % of nominal value at 96 hours, respectively.
- Executive summary:
The study was conducted in accordance with EEC Methods for Determination of Ecotoxicity Annex to Directive 92/69/EEC (OJ. No. L383A, 29.12.92) Part C, Method 1 'Acute toxicity for Fish' which is in most parts equivalent to the OECD Guideline for Testing of Chemicals No. 203 'Fish, Acute Toxicity Test'.
Groups of ten fish of the recommended size were exposed to a limit test concentration of nominally 100 mg/L test item dissolved in water. Auxiliaries used to prepare the test media were an ultrasonic bath, a magnetic stirrer and a folded filter. Observations were made on the number of dead fish and the incidence of sub-lethal effects after 2, 24, 48, 72 and 96 hours of exposure.
The following values were determined:
Time [h] LC50 [mg/L] 2 > 100 24 > 100 48 > 100 72 > 100 96 > 100
No toxic effects against fish were observed at a test concentration of 100 mg/1 under static test conditions.
All results are expressed in terms of nominal concentrations. Recovery rates corresponds to 84.3 % of nominal value at 0 hours and to 85.4 % of nominal value at 96 hours, respectively.
Reference
Description of key information
No toxic effects against fish were observed at a test concentration of 100 mg/L under static test conditions. All results are expressed in terms of nominal concentrations. Recovery rates corresponds to84.3 % of nominal value at 0 hours and to 85.4 % of nominal value at 96 hours, respectively.
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Dose descriptor:
- LC50
- Effect concentration:
- > 100 mg/L
Additional information
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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