Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 422-120-6 | CAS number: 166432-53-7
- 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
![](https://echa.europa.eu/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_ecotoxicological-information.png)
Long-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- long-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 05-02-2002 to 28-01-2003
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study performed under GLP. All relevant validity criteria were met.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 211 (Daphnia magna Reproduction Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.20 (Daphnia magna Reproduction Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- inspected: February 2000 ; signature: April 2000
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 0 (control), 0.0040, 0.013, 0.040, 0.1300, 0.40 mg/L nominal concentration
Time Weighted Mean Measured equivalent concentrations: 0 (control), of 0.0017, 0.0039, 0.012, 0.041 and 0.18 mg/L
- Sampling method: Water samples were taken from the control and each surviving test group (replicates pooled) for quantitative analysis. Samples of the fresh test preparations were taken on Days 0, 3, 7, 10, 14, 17
and 20 and of the expired test preparations on Days 1, 4, 8, 11, 15, 18 and 21. Where possible all samples were prepared for analysis on the day of sampling. Duplicate samples were taken and stored frozen (approximately -20°C) for further analysis if necessary.
- Sample storage conditions before analysis: See above. - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: Direct dissolution of test item in culture medium to prepare stock; serial dilution of stock to prepare test media. An amount of test item (5.50 g) was dispersed in 11 litres of reconstituted water and stirred
with a propeller stirrer (approximately 2000 rpm) for a period of 24 hours at 25°C. After 24 hours stirring the mixture was cooled to approximately 21 °C prior to filtration (0.2 microns) through a Suporcap (first 1 - 2 litres discarded to precondition the filter) to give a saturated solution of approximately 11 mg/L (based on the results obtained for the acute toxicity to Daphnia magna test (cited in full study report). An aliquot of the saturated solution (200 mL) was dispersed in a final volume of 2 litres of reconstituted water to give a nominal 1.1 mg/L stock solution. Aliquots of this nominal 1.1 mg/L stock solution (7.2, 23.6, 72.8, 236 and 728 ml) were each separately dispersed in a final volume of 2 litres of reconstituted water to give nominal test concentrations of0.0040, 0.013, 0.040, 0.13 and 0.40 mg/L. The concentration and stability of the test item in the test preparations were verified by chemical analysis on Days 0, 3, 7, 10, 14, 17 and 20 (fresh media) and on Days I, 4, 8, 11, 15, 18 and 21 (old media). Analysis of the freshly prepared test solutions throughout the test showed the measured test concentrations to range from 0.00344 mg/L to 0.427 mg/L throughout the test (equivalent to a range of 69% to I 07% of the expected nominal values). The majority of samples were observed to be within the accepted range of between 80% to 120% of nominal.
- Chemical name of vehicle (organic solvent, emulsifier or dispersant): Not applicable.
- Concentration of vehicle in test medium (stock solution and final test solution): Not applicable.
- Evidence of undissolved material (e.g. precipitate, surface film, etc): No precipitate reported. - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Daphnia magna
- Strain: not reported
- Source: in-house laboratory cultures
- Age at study initiation (mean and range, SD): < 24 hours
- Method of breeding: Parthenogenesis
- Feeding during test: Yes. The daphnids were fed daily during the study ad libitum with algae suspension
- Food type: algae suspension [unicellular algal culture (Chlorella sp.)]
- Amount: Approximately 0.1 - 0.2 mg carbon/daphnid/day, dependent on the age and size of the animals. Equal amounts of food were given to each daphnid.
- Frequency: Daily
ACCLIMATION
- Acclimation period: None reported. Can be presumed to be < 2 hours in dilution water.
- Acclimation conditions (same as test or not): Yes.
- Type and amount of food: Not applicable.
- Feeding frequency: Not applicable.
- Health during acclimation (any mortality observed): No. - Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 21 d
- Remarks on exposure duration:
- In accordance with the OECD TG 211 guideline.
- Hardness:
- Water hardness was observed to be in the range 248 to 269 mg/L as CaCO3 in the control and the highest surviving test group throughout the test
- Test temperature:
- Actual: 21ºC (throughout test period)
- pH:
- Control: 0 hours to 21 days: pH 7.9 – 8.1 ; test groups: 0 hours to 21 days: pH 7.9 – 8.1
It was considered that there was no treatment related differences to pH - Dissolved oxygen:
- Control: 0 hours to 21 days: 8.1 - 8.6 mg O2/L (90 - 97% ASV) ; test groups: 0 hours to 21 days: 7.9 - 8.6 mg O2/L (90-97% ASV).
It was considered that there was no treatment related differences to oxygen concentration - Salinity:
- Not applicable.
- Conductivity:
- Not applicable.
- Nominal and measured concentrations:
- Concentrations: 0 (control), 0.0040, 0.013, 0.040, 0.1300, 0.40 mg/L nominal concentration
Time Weighted Mean Measured equivalent concentrations: 0 (control), of 0.0017, 0.0039, 0.012, 0.041 and 0.18 mg/L - Details on test conditions:
- TEST SYSTEM
- Test vessel: 150 mL glass flasks
- Type (delete if not applicable): closed (covered to reduce evaporation)
- Material, size, headspace, fill volume: 100 mL fill volume, 50 mL headspace
- Aeration: No. Diluent water was aerated before use.
- Type of flow-through (e.g. peristaltic or proportional diluter): Not applicable.
- Renewal rate of test solution (frequency/flow rate): 3 days renewal.
- No. of organisms per vessel: 1 per 100 mL vessel
- No. of vessels per concentration (replicates): 10 replicates.
- No. of vessels per control (replicates): 10 replicates.
- No. of vessels per vehicle control (replicates): Not applicable.
- Biomass loading rate: equivalent to 100 mL test media per animal.
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: reconstituted water - analytical grade salts dissolved in purified water equivalent or similar to ISO Test water, according to OECD 202, Annex 3: composition (mg/L): KCl 5.8; NaHCO3: 64.8; CaCl2.2H2O: 294 ; MgSO4.7H2O: 123. pH 7.8 (adjusted if necessary).
- Total organic carbon: Not reported
- Particulate matter: Not reported
- Metals: Not reported
- Pesticides: Not reported
- Chlorine: Not reported
- Alkalinity: Not reported
- Ca/mg ratio: Not reported
- Conductivity: <5 µS/cm
- Culture medium different from test medium: No
- Intervals of water quality measurement: Daily, before and after renewal every other alternate day (3 day media renewal).
OTHER TEST CONDITIONS
- Adjustment of pH: No.
- Photoperiod: 16 h light / 8 hours dark, 20 minute dawn and dusk transition periods.
- Light intensity: 583 – 610 lux
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Reproduction and Immobility (or adverse effects including mortality)
- On a daily basis the numbers of live and dead of the "Parental" (P1) generation, the numbers of live and dead "Filial" (F1) Daphnids and the number of discarded unhatched eggs were counted. An assessment was also made of the general condition and size of the parental Daphnids as compared with the controls.
- The number of Daphnids with eggs or young in the brood pouch were determined daily with the exception of days 3, 4, 17 and 18. Young daphnids were considered to be dead if no sign of movement was apparent during microscopic examination. Adult Daphnia which were unable to swim for approximately 15 seconds after gentle agitation (ie. immobile), were considered to be dead.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: Based on preceding acute toxicity study (information in the full study report).
- Justification for using less concentrations than requested by guideline: Not applicable.
- Range finding study
- Test concentrations: Not applicable.
- Results used to determine the conditions for the definitive study: Not applicable. - Reference substance (positive control):
- no
- Duration:
- 21 d
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.004 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- test mat.
- Basis for effect:
- reproduction
- Remarks on result:
- other: (95% CL. - mg/L) ; time weighted mean measured concentration
- Duration:
- 21 d
- Dose descriptor:
- LOEC
- Effect conc.:
- 0.012 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- test mat.
- Basis for effect:
- reproduction
- Remarks on result:
- other: (95% CL. - mg/L) ; time weighted mean measured concentration
- Duration:
- 21 d
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.004 - < 0.012 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- test mat.
- Basis for effect:
- reproduction
- Remarks on result:
- other: (95% CL. - mg/L) ; time weighted mean measured concentration
- Duration:
- 21 d
- Dose descriptor:
- EC50
- Effect conc.:
- 0.008 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- test mat.
- Basis for effect:
- immobilisation
- Remarks on result:
- other: (95% CL. 0.0062 - 0.0096 mg/L) ; ; time weighted mean measured concentration
- Details on results:
- - Behavioural abnormalities: None reported.
- Observations on body length and weight: In P1 generation: There was a significant effect on size and colour of the daphnids in that all the surviving daphnids at 0.40 mg/1 were observed to be markedly smaller and paler in colour than the control animals from Day 4 until 100% mortalities were observed on Day 11. surviving daphnids at 0.13 mg/L were also observed to be paler than the control animals on Days 9 and 11. On Day 12 100% immobilisation was observed at this test concentration. At 0.040 mg/L one out of four daphnids was observed to be small and pale on Day 12 and one out of two daphnids was observed to be pale when compared to the control animals on Days 15 and 16. The daphnids at the remaining test concentrations were observed to be the same size and colour as the control animals. In F1 generation: there was no noted differences to controls.
- Other biological observations: None.
- Mortality of control: No mortalities in control.
- Other adverse effects control: None reported.
- Abnormal responses: None reported.
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: It was speculated the decline in measured test concentrations was due to possible: losses to volatility, adsorption and biological effects and/or to any algae food/organic waste matter present in the test system.
- Effect concentrations exceeding solubility of substance in test medium: No. - Reported statistics and error estimates:
- EC50 (immobilisation) values and associated confidence limits at 6, 7, 14 and 21 days were calculated by the trimmed Spearman-Karber method (Hamilton et al.,1977) using the ToxCalc software package (ToxCalc, 1999).
EC50 (reproduction) was estimated by inspection of the data.
NOEC was estimated using one way analysis of variance incorporating Bartlett's test for homogeneity of variance (Sokal and Rohlf, 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett, 1955)
Reproduction – live young per adult:
- Results from the control, 0.0080, 0.025 and 0.080 mg/L test groups were compared using one way analysis of variance incorporating Bartlett's test for homogeneity of variance (Sokal and Rohlf, 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett, 1955).
- 0.13 and 0.40 mg/L test groups data were not included in the statistical analysis as the effects of exposure eliminated all the daphnids prior to termination of the test.
- No significant differences (P≥0.05) were found between the control, 0.0040 and 0.013 mg/L test groups in terms of the number of live young produced per adult by Day 21
Length data:
- Results from the control, 0.0040 and 0.013 mg/L test groups Daphnia length data, determined for the surviving daphnids on termination of the test were compared using one way analysis of variance incorporating Bartlett' s test for homogeneity of variance (Sokal and Rohlf, 1981) and Dunnett's multiple comparison procedure for comparing several treatments with a control (Dunnett, 1955).
- 0.13 and 0.40 mg/L groups data were not included in the statistical analysis as the effects of exposure eliminated all the daphnids prior to termination of the test.
- No significant differences (P≥0.05) were found between the control, 0.0040 and 0.013 mg/L test groups in terms of the number of live young produced per adult by Day 21 - Validity criteria fulfilled:
- yes
- Conclusions:
- The test item 21d-NOEC was 0.0039 mg/L. The 21-d EC50 (reproduction) was between 0.0039 and 0.012 mg/L. All effects were based on time weighted mean measured concentrations.
- Executive summary:
The 21-d reproduction toxicity to Daphnia magna was carried out according to OECD TG 211 and EU Method C.20 guidelines under GLP. Based on the results of an acute toxicity test, Daphnia magna were exposed (10 replicates of a single daphnid per group) to an aqueous solution of the test item over a range of nominal test concentrations of0 (control), 0.0040, 0.013, 0.040, 0.1300, 0.40 mg/Lfor a period of 21 days. The test concentrations were prepared by dilution of a saturated solution of the test item. The saturated solution was prepared by stirring an excess of test material in test medium for a period of 24 hours prior to removal of the excess test material by filtration (0.2 µm). Test concentrations were prepared by dilution of a saturated solution of the test item. The saturated solution was prepared by stirring an excess of test item in test medium for a period of 48 hours prior to removal of the excess test item by filtration (0.2 µm). The test solutions were renewed daily (or > 3 times per week). Daphnids were fed daily with algal suspension. The numbers of live and dead adult (P1) daphnids and (F1) young daphnids was determined daily. It was considered validity criteria of the test guideline were fulfilled. Analysis of the saturated solution used to prepare the test concentrations throughout the test showed the measured test concentrations to range from 9.1 mg/L to 10 mg/L (82% to 94% of the expected nominal value). These results were consistent with the results from the pre-test preparation trials (11 mg/L) and the water solubility value of 10.1 mg/L. Analysis of the freshly prepared test solutions throughout the test showed the measured test concentrations to range from 0.00344 mg/L to 0.427 mg/L throughout the test (equivalent to a range of 69% to 107% of the expected nominal values). The majority of samples were observed to be within the accepted range of between 80% to 120% of nominal. On this basis it was considered appropriate to base effect level estimates on time weighted mean measured concentrations. The test item 14-d EC50 (immobilisation) was 0.0087 (C.I. 0.0064 – 0.0017) mg/L and 21-d EC50 (immobilisation) was 0.0077 (C.I. 0.0062 – 0.0096) mg/L. The test item 21-d EC50 (reproduction) was between 0.0039 and 0.012 mg/L based on time weighted mean measured concentrations. There was no significant difference (P ≥ 0.05) in terms of the number of young produced per adult when compared to the control and that the adult daphnids at 0.0039 mg/L were eliminated from the test by Day 21 due to a prolonged toxic effect of the test item. The test item 21d-NOEC was 0.0039 mg/L based on time weighted mean measured concentrations.
Reference
All validity criteria were considered to be met:
1. Control mortality was ≤20% (actual 0%)
2. Dissolved oxygen was maintained ≥ 3 mg O2/L (actual ≥ 8.0 mg O2/L)
3. pH control group ≤ 1.5 deviation (actual 1.4)
5. Mean live young per surviving adult ≥ 60 after 21 days (actual 65)
6. CoV for control group ≤ 25% (actual 21%)
Description of key information
21d-NOEC (invertebrates, reproduction) = 0.0039 mg/L based time weighted mean measured concentrations, 21-days freshwater, OECD TG 211, 2003
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 0.004 mg/L
Additional information
Key study : OECD TG 211, 2003 : The 21-d reproduction toxicity to Daphnia magna was carried out according to OECD TG 211 and EU Method C.20 guidelines under GLP. Based on the results of an acute toxicity test, Daphnia magna were exposed (10 replicates of a single daphnid per group) to an aqueous solution of the test item over a range of nominal test concentrations of0 (control), 0.0040, 0.013, 0.040, 0.1300, 0.40 mg/Lfor a period of 21 days. The test concentrations were prepared by dilution of a saturated solution of the test item. The saturated solution was prepared by stirring an excess of test material in test medium for a period of 24 hours prior to removal of the excess test material by filtration (0.2 µm). Test concentrations were prepared by dilution of a saturated solution of the test item. The saturated solution was prepared by stirring an excess of test item in test medium for a period of 48 hours prior to removal of the excess test item by filtration (0.2 µm). The test solutions were renewed daily (or > 3 times per week). Daphnids were fed daily with algal suspension. The numbers of live and dead adult (P1) daphnids and (F1) young daphnids was determined daily. It was considered validity criteria of the test guideline were fulfilled. Analysis of the saturated solution used to prepare the test concentrations throughout the test showed the measured test concentrations to range from 9.1 mg/L to 10 mg/L (82% to 94% of the expected nominal value). These results were consistent with the results from the pre-test preparation trials (11 mg/L) and the water solubility value of 10.1 mg/L. Analysis of the freshly prepared test solutions throughout the test showed the measured test concentrations to range from 0.00344 mg/L to 0.427 mg/L throughout the test (equivalent to a range of 69% to 107% of the expected nominal values). The majority of samples were observed to be within the accepted range of between 80% to 120% of nominal. On this basis it was considered appropriate to base effect level estimates on time weighted mean measured concentrations. The test item 14-d EC50 (immobilisation) was 0.0087 (C.I. 0.0064 – 0.0017) mg/L and 21-d EC50 (immobilisation) was 0.0077 (C.I. 0.0062 – 0.0096) mg/L. The test item 21-d EC50 (reproduction) was between 0.0039 and 0.012 mg/L based on time weighted mean measured concentrations. There was no significant difference (P ≥ 0.05) in terms of the number of young produced per adult when compared to the control and that the adult daphnids at 0.0039 mg/L were eliminated from the test by Day 21 due to a prolonged toxic effect of the test item. The test item 21d-NOEC was 0.0039 mg/L based on time weighted mean measured concentrations.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
![ECHA](/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/echa_logo.png)