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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 225-208-0 | CAS number: 4719-04-4
- 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
Toxicity to aquatic algae and cyanobacteria
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Vehicle:
- no
- Details on test solutions:
- - The test substance was stirred in demineralized water for about 20 minutes at approximately 20 +/- °C.
- The nominal concentration of the stock solution was 125 mg/L.
- The pH-value of 9.9 of the stock solution was adjusted to 7.6. - Test organisms (species):
- Desmodesmus subspicatus (previous name: Scenedesmus subspicatus)
- Details on test organisms:
- - Pre-culture techniques: a seed culture was incubated for 7 days at 23 °C +/- 2°C final cell density 384 x 10E04cells/ml
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Test temperature:
- 23 °C
- pH:
- 7.9 - 8.1
- Nominal and measured concentrations:
- - Nominal test concentrations (mg/L): 0, 0.39, 0.78, 1.56, 3.13, 6.25, 12.5, 25, 50, 100
- The analytical verifications of the test substance were investigated at different concentrations in OECD-medium. The analytical results yielded 80 % or higher recoveries; they varied between 101 and 110 % of the nominal concentrations at test initiation and between 103 to 108 % at test termination. Therefore, all biological results are related to the nominal concentrations of the test item. - Details on test conditions:
- - Test vessels: Erlenmeyer flasks (nominal volume 250 mL) plugged with gas permeable siliconsponge caps
- Test volume: 100 mL
- Number of replicates/conc.: 3
- Number of replicates/conc.: 3
- Illumination: artificial light, type universal white (e.g. Osram L 25), permanent illumination
- Light intensity: about 60 - 120 µE/(m2xs) at a wave length of 400 - 700 nm
- Measurement of fluorescence: after 0, 24, 48 and 72 h
- Cell counting: after 72 h in a counting chamber (Neubauer improved)
- Measurement of temperature: continuously during the whole test period in the climate chamber
- Measurement of pH-values: after 0 h and 72 h in an additional uninoculated replicate and after 72 h in the inoculated replicate No. 1 of each concentration - Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 1.56 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- LOEC
- Effect conc.:
- 3.13 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- 3.4 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 6.66 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC90
- Effect conc.:
- 10.4 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Validity criteria fulfilled:
- yes
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2005-10-07 to 2006-01-17
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- The purity of the test substance is not indicated, no analytical monitoring was performed.
- Qualifier:
- according to guideline
- Guideline:
- ISO 10253 (Water quality - Marine Algal Growth Inhibition Test with Skeletonema costatum and Phaeodactylum tricornutum)
- Version / remarks:
- 1998
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: US EPA (1985) Methods for measuring the acute toxicity of effluents to freshwater and marine organisms. EPA/600/4-85/013.
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: ISO 5667-16 (1998) Water quality sampling -guidance on biotesting on samples.
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Details on sampling:
- Not applicable
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: The test substance was prepared as a water accomodated fractions (WAFs). WAFs were prepared by the direct addition of the required nominal weights or volumes to seawater followed by gentle stirring for approximately 20 hours followed by a settling period of approximately one hour. After this settling period, the middle phase of the preparation is siphoned, avoiding incorporation of undissolved particles, if present. - Test organisms (species):
- Skeletonema costatum
- Details on test organisms:
- TEST ORGANISM
- Common name: Skeletonema costatum
- Method of cultivation: The cultures were cultivated by inoculating nutrient medium (ISO culture medium) to a cell density of approximately 2 x 10^3 to 10^4 cells per millilitre.
The pre-cultures were incubated at approximately 20 +/- 2 °C under constant illumination for 3d +/- 1d and were used as the inoculum source for subsequent toxicity tests.
- Test type:
- static
- Water media type:
- saltwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Post exposure observation period:
- none
- Hardness:
- no data
- Test temperature:
- 20.4 - 21.6 °C
- pH:
- 8.18 - 8-68
- Dissolved oxygen:
- not measured
- Salinity:
- no data
- Conductivity:
- 51.2 - 52.1 mS/cm
- Nominal and measured concentrations:
- Nominal concentrations: 1.0, 3.2, 10, 32, 100 mg/L
No measured concentrations - Details on test conditions:
- TEST SYSTEM
- Test vessel: 100 ml borosilicate glass conical flasks,
- Material, size, headspace, fill volume: 80 ml of test medium seawater was added.
- Renewal rate of test solution: No renewal
- Initial cells density: 146.5 x 10 ^4 cells mL
- No. of organisms per vessel: Approximately 10^4 cells per millilitre.
- No. of vessels per concentration: 3
- No. of vessels per control: 4
GROWTH MEDIUM
- Standard medium used: yes
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: ISO medium is prepared from natural seawater supplied by pump from Scapa Flow, Orkney. All seawater was UV sterilised and filtered to 0.2 µm. The filtered treated seawater was then enriched with nutrients and vitamins in accordance with ISO guidelines.
- Conductivity: 51.2 - 52.1 mS/cm
OTHER TEST CONDITIONS
- Adjustment of pH: no
- Photoperiod: Constant illumination for 3 d +/- 1 d
- Light intensity and quality: 7460 (0h), 7690 (24 h), 7080 (48h), 7430 (72h) lux
EFFECT PARAMETERS MEASURED:
- Determination of cell concentrations: Counts of algal cell numbers were carried out daily by microscope using either haemocytometer or Sedgewick-Rafter chamber, depending upon cell numbers present or by Fluorometer measurements. Three readings were performed on each test vessel.
TEST CONCENTRATIONS
- Range finding study: Rangefinding tests were conducted over 72h to determine the approximate concentrations at which effects were observed.
- Test concentrations: 1.0, 3.2, 10, 32, 100 mg/L - Reference substance (positive control):
- yes
- Remarks:
- 3.5 Dichlorophenol
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 21 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Remarks on result:
- other: 95 % Confidence limits: 18.85 - 21 mg/L
- Key result
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 10 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC90
- Effect conc.:
- 29.8 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 8.17 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: biomass integral
- Details on results:
- - Other: There was a difference in results between the rangefinding and definitive tests, possibly due to flask contamination or insufficient cells added.
In the first definitive test there was growth at 10 mg/L^-1, the highest test concentration.
The second definitive test range was therefore derived from the initial definitive test and was 1.0, 3.2, 10, 32 and 100 mg/L^-1, the 72h EC50 was 18.71 mg/L^-1.
A third definitive test was requested by the client with three replicates per test concentration and the 72h EC50 was 21.00 mg/L^-1 (water accommodated fractions) to the marine phytoplankton Skeletonema costatum in the aqueous phase. - Results with reference substance (positive control):
- - Results with reference substance valid: Yes
- EC50: The 72 h EC50 was determined to be 3.82 mg/L - Validity criteria fulfilled:
- yes
Referenceopen allclose all
Inhibition related to biomass
EbC10 = 2.13 mg/L
EbC50 = 4.34 mg/L
EbC90 = 7.98 mg/L
Description of key information
Freshwater: The test substance was tested in an OECD guideline 201 study with Desmodesmus subspicatus. The EC50 was determined to be 6.66 mg/L and EC10 was determined to be 3.4 mg/L.
Saltwater: The test substance was tested in a guideline study with Skeletonema costatum. The test substance exhibited a 72 h EC50 of 21 mg/L and a NOEC value of 10 mg/L.
Key value for chemical safety assessment
- EC50 for freshwater algae:
- 6.6 mg/L
- EC50 for marine water algae:
- 21 mg/L
- EC10 or NOEC for freshwater algae:
- 3.4 mg/L
- EC10 or NOEC for marine water algae:
- 10 mg/L
Additional information
Freshwater
Key
The test substance was tested in an OECD guideline 201 study with Desmodesmus subspicatus. The nominal concentrations tested were 0, 0.39, 0.78, 1.56, 3.13, 6.25, 12.5, 25, 50, 100 mg/L. The analytical verifications of the test substance were investigated at different concentrations in OECD-medium. The analytical results yielded 80 % or higher recoveries; they varied between 101 and 110 % of the nominal concentrations at test initiation and between 103 to 108 % at test termination. Therefore, all biological results are related to the nominal concentrations of the test item. The test was conducted under static conditions. The EC50 was determined to be 6.66 mg/L and EC10 was determined to be 3.4 mg/L.
Supporting
The test substance was tested in an OECD guideline study with Desmodesmus subspicatus. The EC50 was determined to be 6.4 mg/L the EC10 was determined to be 5 mg/L.
Conclusion: Two OECD guideline studies were conducted. The results of both studies lay in the same range. As a worst case the EC50 value of 6.66 mg/l and the EC10 value of 3.4 mg/L was chosen as key values.
Salt water
The test substance was tested in a guideline study with Skeletonema costatum. The test substance was added to the test system via water accommodated fractions. 5 nominal concentrations were tested: 1, 3.2, 10, 32 and 1000 mg/L. Pre-cultures in the exponential growth phase were prepared from stock laboratory cultures by inoculating nutrient medium (ISO culture medium) to a cell density of approximately 2 x 10^3 to 10^4 cells per millilitre.The test substance exhibited a 72 h EC50 of 21 mg/L and a NOEC value of 10 mg/L. All relevant validity criteria were met.
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.