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EC number: 500-107-7 | CAS number: 40039-93-8
- 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
- Study period:
- 18/1/2012-4/12/2012
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP comparable to OECD guideline
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.3 (Algal Inhibition test)
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 850.5400 (Algal Toxicity, Tiers I and II) (January 2012)
- Principles of method if other than guideline:
- /
- GLP compliance:
- yes
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material (migrated information):
/ - Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations:all
- Sampling method:Samples of the test solutions were collected at approximately 0 and 96 hours to measure concentrations of the test substance. Samples at test initiation were collected from the individual batches of test solution prepared for each treatment and control group prior to distribution into the test chambers. At exposure termination, samples were collected from the pooled replicates from each treatment and control group. Algal cells were removed prior to analysis during extraction of the test substance from test medium into an organic solvent. Samples were collected directly into glass vessels and processed immediately for analysis.
- Sample storage conditions before analysis: No storage - Vehicle:
- yes
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method:A primary stock solution was prepared by dissolving 0.0101 g of brominated epoxy in 200 mL of tetrahydrofuran (THF; Burdick and Jackson; Lot Number: DF758) to achieve a nominal concentration of 50.5 μg/mL. The primary stock was mixed by inversion and appeared clear and colorless and was otherwise unremarkable. The 50.5 μg/mL stock was serially diluted with THF to prepare six additional stock solutions at target nominal concentrations of 2.3, 4.5, 9.0, 18, 27 and 36 μg/mL. All stock solutions were mixed by inversion. The test solutions were prepared by adding 1.0 mL of each respective stock stock solution (except the 50.5 μg/mL primary stock) into 1L volumetric flasks. The solvent (THF) within each flask was then evaporated under a stream of nitrogen until dryness (approximately 5 minutes). The flasks were then brought to a final volume of 1L with freshwater AAP medium (INV#12-167), inverted at least twenty times and sonicated for approximately 5 minutes to mix.
- Controls:The negative control solution consisted of freshwater AAP medium without test substance added.
- Chemical name of vehicle (organic solvent, emulsifier or dispersant):tetrahydrofuran (organic solvent)
- Concentration of vehicle in test medium (stock solution and final test solution(s) including control(s)): 0, the solvent (THF) within each flask was evaporated under a stream of nitrogen until dryness
- Evidence of undissolved material (e.g. precipitate, surface film, etc):No - Test organisms (species):
- Raphidocelis subcapitata (previous names: Pseudokirchneriella subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- TEST ORGANISM
- Source (laboratory, culture collection): University of Toronto, and have been maintained in culture medium at Wildlife International, Easton, Maryland since March 2000.
- Age of inoculum (at test initiation): at least two weaks
- Method of cultivation: growing in culture medium under the same environmental conditions as used in this test
ACCLIMATION
- Acclimation period: No
- Culturing media and conditions (same as test or not): Freshwater AAP medium.
- Any deformed or abnormal cells observed:No - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Post exposure observation period:
- /
- Hardness:
- No data
- Test temperature:
- 24 +/- 2 °C
- pH:
- Start: 7.45, End: 9.15
- Dissolved oxygen:
- No data
- Salinity:
- No data
- Nominal and measured concentrations:
- Nominal concentrations: 2.3; 4.5; 9.0; 18; 27; 36 µg/L
Measured concentrations: 1.8; 3.9; 7.6; 15; 24; 30 µg/L - Details on test conditions:
- TEST SYSTEM
- Test vessel:Test chambers were sterile, 250 mL glass Erlenmeyer flasks plugged with sterile foam stoppers, and contained 100 mL of test or control medium.
- Initial cells density:10 000 cells/mL
- Control end cells density: 4 510 000cells/mL
- No. of organisms per vessel: 2020 cells
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates):6
- No. of vessels per vehicle control (replicates):/
GROWTH MEDIUM
- Standard medium used: yes
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water:purified well water (NANOpure® water)
- Metals:See Appendix 4
- Pesticides: See Appendix 4
OTHER TEST CONDITIONS
- Sterile test conditions: yes
- Adjustment of pH: using 10% hydrochloric acid
- Photoperiod:continuous cool-white fluorescent lighting throughout the test
- Light intensity and quality:. The target light intensity was 6,000 lux ± 10%
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
- Determination of cell concentrations:hemacytometer and microscope
TEST CONCENTRATIONS
- Spacing factor for test concentrations:2
- Test concentrations: 2.3; 4.5; 9.0; 18; 27 and 36 µg/mL
TEST CONCENTRATIONS RANGE FINDING STUDY
- Spacing factor for test concentrations: 2
- Range finding study: Yes
- Test concentrations: 9.0; 18; 36 µg/L
- Results used to determine the conditions for the definitive study: Yes - Reference substance (positive control):
- no
- Duration:
- 96 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 30 µg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- yield
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 30 µg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- yield
- Duration:
- 96 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 30 µg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 30 µg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 96 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 30 µg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- other: Area under the growth curve
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 30 µg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- other: Area under the growth curve
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 30 µg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- other: Area under the growth curve
- Duration:
- 96 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 30 µg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- other: Area under the growth curve
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 30 µg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 96 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 30 µg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 30 µg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- yield
- Duration:
- 96 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 30 µg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- yield
- Details on results:
- - Exponential growth in the control (for algal test): yes
- Observation of abnormalities (for algal test):No
- Unusual cell shape:No
- Colour differences:No
- Flocculation:No
- Adherence to test vessels:No
- Aggregation of algal cells:No
- Other:/
- Any stimulation of growth found in any treatment: a slight stimulation could be observed of max -4% inhibition
- Effect concentrations exceeding solubility of substance in test medium:No - Results with reference substance (positive control):
- /
- Reported statistics and error estimates:
- The calculation of cell densities, area under the growth curve, yield, growth rates and percent inhibition values, as well as all statistical analyses, were conducted using “The SAS System for Windows, Version 8.2” (5).
- Validity criteria fulfilled:
- yes
- Conclusions:
- The freshwater alga, Pseudokirchneriella subcapitata, was exposed to a geometric series of five treatment levels of brominated epoxy ranging from 1.8 to 30 μg/L, based on day 0 measured concentrations of brominated epoxy and one additional level at a day 0 measured concentration of 24 μg/L. Toxicity of brominated epoxy to P. subcapitata was assessed based on effects on area under the growth curve, yield and growth rate relative to the negative control group. None of the treatment groups mean responses for area under the growth curve, growth rate or yield were significantly reduced relative to the mean control responses (Dunnett’s test (p > 0.05). Consequently, the 72 and 96 hour NOEC values were determined to be 30 μg/L for both intervals. The 72 and 96-hour EC50 values for area under the growth curve, yield and growth rate could not be calculated due to the lack of a dose-response and were empirically estimated to be greater than the highest concentration tested, 30 μg/L.
In this study the highest reported water solubility value was lower than the actual value reported in the water solubility study. This difference in solubility values is explained by the hydrophobicity property of the substance and the difference between the experimental media (reagent water vs media with organisms). There is a decrease in concentrations of the test substance along the experiment. - Executive summary:
LENGTH OF EXPOSURE: 96 Hours
TEST ORGANISM: Freshwater Alga (Pseudokirchneriella subcapitata)
SOURCE OF TEST ORGANISMS: Wildlife International Cultures
Easton, Maryland 21601
TEST CONCENTRATIONS:
Nominal (µg/L) Day 0 measured (µg/L) Geometric mean measured (µg/L) Negative control < LOQ < LOQ 2.3 1.8 0.95 4.5 3.9 1.4 9.0 7.6 2.7 18 15 5.4 27 24 6.9 36 30 9.9 36 (abiotic) 30 21 RESULTS
Exposure duration (hours) Area under the growth curve (µg/L) Growth rate (µg/L) Yield (µg/L) NOEC EC50 95% CI NOEC EC50 95% CI NOEC EC50 95% CI 72 30 >30 n/a 30 >30 n/a 30 >30 n/a 96 30 >30 n/a 30 >30 n/a 30 >30 n/a
Reference
Description of key information
Toxicity of brominated epoxy to P. subcapitata
Key value for chemical safety assessment
- EC50 for freshwater algae:
- 30 µg/L
- EC10 or NOEC for freshwater algae:
- 30 µg/L
Additional information
The freshwater alga, Pseudokirchneriella subcapitata, was exposed to a geometric series of five treatment levels of brominated epoxy ranging from 1.8 to 30 μg/L, based on day 0 measured concentrations of brominated epoxy and one additional level at a day 0 measured concentration of 24 μg/L. Toxicity of brominated epoxy to P. subcapitata was assessed based on effects on area under the growth curve, yield and growth rate relative to the negative control group. None of the treatment groups mean responses for area under the growth curve, growth rate or yield were significantly reduced relative to the mean control responses (Dunnett’s test (p > 0.05). Consequently, the 72 and 96 hour NOEC values were determined to be 30 μg/L for both intervals. The 72 and 96-hour EC50 values for area under the growth curve, yield and growth rate could not be calculated due to the lack of a dose-response and were empirically estimated to be greater than the highest concentration tested, 30 μg/L. Note that 30 µg/L is the highest solubility level that could be tested.
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