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EC number: 252-044-7 | CAS number: 34455-00-0
- 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:
- 08 Nov - 10 Dec 2010
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Freshwater Alga and Cyanobacteria, Growth Inhibition Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.3 (Algal Inhibition test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- ISO 8692 (Water Quality - Fresh Water Algal Growth Inhibition Test with Scenedesmus subspicatus and Selenastrum capricornutum)
- Deviations:
- no
- GLP compliance:
- yes
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No.of test material: 124691-59B
- Physical state: White solid
- Analytical purity: 97.6 %
- Expiration date of the lot/batch: 01 July 2012
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: At room temperature in the dark
- Stability under test conditions: Stable - Analytical monitoring:
- yes
- Details on sampling:
- Concentrations: All concentrations monitored
- Sampling method: One 2-mL sample was taken from all test concentrations and the control at times zero, 24h and 72h. One sample was held in reserve. A separate vessel was made for analytical sampling. At the end of the exposure period, the replicates with algae were pooled at each concentration before sampling.
- Sample storage conditions before analysis: Stored frozen
- Abiotic samples: To verify maintanence of test substance concentration, a test vessel was set up at the highest substance concentration but without algae. Samples for analysis were taken at times zero, 24h and 72h.- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: Preparation of test solutions started with a concentration of 100 mg/L applying an overnight period of magnetic stirring to accelerate the dissolution of test substance in medium. The lower concentrations were prepared by subsequent dilutions of the highest concentration in test medium.
- Controls: Test medium without test substance or other additives
- Evidence of undissolved material (e.g. precipitate, surface film, etc.): none, test solutions were clear and colorless at start of test - Test organisms (species):
- Raphidocelis subcapitata (previous names: Pseudokirchneriella subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- TEST ORGANISM
- Common name: Pseudokirchneriella subcapitata
- Strain: NIVA CHL 1
- Source (laboratory, culture collection): In-house laboratory culture
- Method of cultivation: Stock cultures were maintained in M1 medium (Nederlandse Praktijk Richtlijn no. 6505).
NaNO3, 500 mg/l
K2HPO4∙3H2O, 52 mg/l
MgSO4∙7H2O, 75 mg/l
Na2CO3∙10H2O, 54 mg/l
C6H8O7∙H2O, 6 mg/l
NH4NO3, 330 mg/l
CaCl2∙2H2O, 35 mg/l
C6H5FeO7∙xH2O, 6 mg/l
H3BO3, 2∙9 mg/l
MnCl2∙4H2O, 1.81 mg/l
ZnCl2, 0.11 mg/l
CuSO4∙5H2O, 0.08 mg/l
(NH4)6Mo7O24∙4H2O, 0.018 mg/l
ACCLIMATION
Four days before the start of the test, cells from the algal stock culture were inoculated in OECD medium at a cell density of 1e+04 cells/mL. The pre-culture was maintained under the same conditions as used in the test. The cell density was measured immediately before use. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Hardness:
- 24 mg CaCO3/L
- Test temperature:
- 22.1 - 24.0 °C
- pH:
- 7.8 - 8.2
- Nominal and measured concentrations:
- Nominal: 0 mg/L, 10 mg/L, 18 mg/L, 32 mg/L, 56 mg/L, 100 mg/L
Measured: see Table 1 - Details on test conditions:
- TEST SYSTEM
- Test vessel: 100 mL, all-glass. Fill volume was 50 mL
- Agitation: Yes, during incubation the algal cells were kept in suspension by continuous shaking.
- Initial cells density: 1E+04 cells/mL
- Control end cells density: 124.4E+04 cells/mL
- No. of vessels per concentration (replicates): 3
- No. of vessels per control (replicates): 6
1 replicate of the highest concentrations without algae
1 or 2 replicates of each test concentration for sampling
GROWTH MEDIUM
- Standard medium used: Yes - OECD medium
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Milli-Q water (tap water purified by reverse osmosis and subsequently passed over activated carbon and ion-exchange cartridges)
- Culture medium different from test medium: yes, propagation in M1, but a pre-culture was established in OECD medium 4 days before test initiation to use in test
- Intervals of water quality measurement: pH at beginning and 72 hours, temperature continuously
OTHER TEST CONDITIONS
- Adjustment of pH: No
- Photoperiod: continuous illumination using 30 Watt 'Cool-white' TLD-Iamps. Light intensity within the range of 88 to 95 µE.m-2.s-1.
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
- Determination of cell concentrations: Beginning of the test, cells were counted with a microscope and counting chamber. Thereafter cell densities were measured using a spectrophotometer with immersion probe (pathlength = 10 mm). At the end of the study final microscopic observations were made on the highest test concentration to observe for any abnormal appearance of the algae.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 1.8
- Range finding study: Yes
- Test concentrations: 0.10, 1.0, 10 and 100 mg/L
- Results used to determine the conditions for the definitive study: Yes - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- 19 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Remarks on result:
- other: 95% CI: 13-28 mg/L
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 10 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Details on results:
- - Exponential growth in the control (for algal test): yes. The mean CV for section specific growth rates in the control was 18%, and the CV of average specific growth rates during the whole test period in control was 3%.
- Observation of abnormalities (for algal test): None observed. Microscopic observations at the end of the test revealed a normal and healthy appearance of the algal cells exposed to highest concentration when compared to the control.
- Any stimulation of growth found in any treatment: no
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: no
- Effect concentrations exceeding solubility of substance in test medium: yes - Results with reference substance (positive control):
- - Results with reference substance valid? yes
- ErC50: 1.4 mg/L. The historical ranges for growth rate reduction lie between 0.82 and 2.3 mg/L.
- Other: Reference substance toxicity assay conducted 77 days before the test substance assay. - Reported statistics and error estimates:
- Growth rate data were normally distributed by Chi-squared test, p = 0.4231 > 0.01. Variance of growth rate data were homogeneous by Levene's test, p(F) = 0.7579 > 0.01. NOEC was determined using Bonferroni t-test (α = 0.05). Calculation of the EC10 value was based on log-linear regression analysis of the percentages of growth rate reduction versus the logarithms of the corresponding nominal concentrations of the test substance. Statistical calculations were done in TOXSTAT Release 3.5, 1996.
- Validity criteria fulfilled:
- yes
- Remarks:
- Control cell density increased by an average factor of >16 within 2 days, the mean CV for section specific growth rates in the control was < 35% (18%), and the CV of average specific growth rates during the whole test period in control was < 7% (3%).
- Conclusions:
- The 72-hour EC50 (growth rate) of FBSEE diol to Pseudokirchneriella subcapitata was beyond the range tested (nominal concentration of 100 mg/L). The corresponding 72-hour NOEC (growth rate) was 10 mg/L. Test conducted per OECD 201.
- Executive summary:
The toxicity of FBSEE diol to the green algae, Pseudokirchneriella subcapitata, was assessed in a 72-hour toxicity test conducted according to the OECD 201 method. An exponential growth was observed during the entire period of exposure in the control vessel and the validity criteria were met. Nominal concentrations were confirmed by analytical measurement (98-110%).
The 72-hour ErC50 of FBSEE diol to Pseudokirchneriella subcapitata for growth rate was beyond the range tested (nominal concentration of 100 mg/L). The corresponding 72-hour NOEC (growth rate) was 10 mg/L and the 72-hour ErC10 was 19 mg/L (95% CI: 13-28 mg/L).
The study was performed in accordance with internationally-accepted test guidelines under GLP. The study is deemed reliable without restriction and suitable for use in Risk Assessment, Classification & Labeling, and PBT Analysis.
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 20-June-2011 to 24-June-2011
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Freshwater Alga and Cyanobacteria, Growth Inhibition Test)
- Deviations:
- no
- GLP compliance:
- no
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Physical state: white powder
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: store away from heat - Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: Initially a 100 mg/l solution was prepared by dilutiing 0.180 grams of FBSEE diacid to 1.8 liters of test media. The 100 mg/L solution was stirred on a magnetic stir plate for two hours to ensure complete solubility of FBSEE diacid in the dilution water. The 100 mg/L solution was then used to prepare lesser test concentrations.
- Controls: Test medium without test substance or other additives
- Evidence of undissolved material: Visual observations of the test solutions did not show any color change or precipitates. - Test organisms (species):
- Raphidocelis subcapitata (previous names: Pseudokirchneriella subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- TEST ORGANISM
- Common name: Pseudokirchneriella subcapitata 22662
- Source (laboratory, culture collection): strain from American Type Culture Collection
ACCLIMATION
- Acclimation period: Algal stock was subcultured in OECD recommended medium for 8 days before test initiation
- Culturing media and conditions (same as test or not): Same - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Test temperature:
- 23.1 - 23.4 °C
- pH:
- 6.26 - 9.57
- Conductivity:
- 195 - 216 µmhos/cm
- Nominal and measured concentrations:
- Nominal concentrations: 0 (dilution water control), 6.3 mg/L, 12.5 mg/L, 25 mg/L, 50 mg/L, 100 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel: Erlenmeyer flasks
- Type: closed with foam stoppers
- Material, size, headspace, fill volume: borosilicate glass, 250 mL with 100 mL fill volume
- Aeration: test vessels held on shaker table set at 100 rpm
- Initial cells density: 2.4E+04 cells/mL
- Control end cells density: 49.5E+04 cells/mL
- No. of vessels per concentration (replicates): four
- No. of vessels per control (replicates): four
GROWTH MEDIUM
- Standard medium used: Yes, OECD medium
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Deionized water
- Conductivity: 195 - 216 µmhos/cm
- Culture medium different from test medium: No
- Intervals of water quality measurement: At test initiation and termination - pH, conductivity and temperature; daily - temperature
OTHER TEST CONDITIONS
- Sterile test conditions: Test vessels and test medium were autoclaved
- Adjustment of pH: No
- Photoperiod: continuous illumination
- Light intensity and quality: 7920 to 8150 lux, using 30 Watt 'Cool-white' fluorescent Iamps
EFFECT PARAMETERS MEASURED:
- Determination of cell concentrations: Daily cells counts using direct microscopic enumeration via an Improved Neubauer hemacytometer
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2
- Range finding study: yes
- Test concentrations: 0 mg/L, 100 mg/L
- Results used to determine the conditions for the definitive study: yes - Reference substance (positive control):
- no
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 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.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Details on results:
- - Exponential growth in the control (for algal test): yes. The mean CV for section specific growth rates in the control was 6% for the 24 hour test interval and the 48-hour to 96-hour mean CVs ranged from 2-3%. The CV of average specific growth rates during the whole test period in the control was 2%.
- Observation of abnormalities (for algal test): not reported
- Any stimulation of growth found in any treatment: no
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: not reported
- Effect concentrations exceeding solubility of substance in test medium: no - Reported statistics and error estimates:
- Growth rate data were normally distributed by Shapiro - Wilks test, D = 0.0036; W = 0.9777. Variance of growth rate data were homogeneous by Bartlett's test, calculated B1 statistic = 4.2810; p-value = 0.5097. NOEC was determined using Dunnett's test (α = 0.05). The mean coefficient of variation for specific growth rates in control cultures for section-by-section was 6% for the 24-hour test interval. The 48-hour to 96-hour mean coefficient of variations ranged from 2-3%. The coefficient of variation of average specific growth rates in replicate control cultures was 2%. Statistical calculations were done using ICp software (EC10s and EC50s) and TOXSTAT Release 3.5, (NOECs and LOECs).
- Validity criteria fulfilled:
- yes
- Remarks:
- Control cell density increased by a factor of 17 during the first 3 days, the mean CV for section specific growth rates in the control was < 35% (6%), and the CV of average specific growth rates during the whole test period in control was < 7% (2%).
- Conclusions:
- The 72-hour EC50 and EC10 (growth rate) of FBSEE diacid to Pseudokirchneriella subcapitata was beyond the range tested (nominal concentration of 100 mg/L). The test was conducted per OECD TG 201.
- Executive summary:
FBSEE diacid is a degradation product of FBSEE diol. The toxicity of FBSEE diacid to the green algae,Pseudokirchneriella subcapitata, was assessed in a 72-hour toxicity test conducted according to the OECD 201 method. An exponential growth was observed during the entire period of exposure in the control vessel and the validity criteria were met. The 72-hour EC50 and EC10 of FBSEE diacid to Pseudokirchneriella subcapitatafor growth rate were beyond the range tested (nominal concentration of 100 mg/L). The study followed an international standard method but was not GLP compliant. The results are for a degradation product rather than the parent material. Therefore the study is deemed reliable with restrictions.
Referenceopen allclose all
Mean cell densities (x 1e+04 cells/mL)
Nominal conc. (mg/L) |
Exposure time (hours) |
|
|
|
0 |
24 |
48 |
72 |
|
control |
1.0 |
7.0 |
25.2 |
124.4 |
10 |
1.0 |
6.7 |
26.3 |
124.9 |
18 |
1.0 |
6.7 |
20.8 |
85.9 |
32 |
1.0 |
6.7 |
16.9 |
58.6 |
56 |
1.0 |
7.4 |
12.7 |
24.8 |
100 |
1.0 |
7.0 |
11.5 |
14.7 |
Percentage reduction of growth rate at different time intervals
Nominal conc. (mg/L) |
Mean growth rate |
|||||
. | µ (0 -24 h) |
Reduction (%) |
µ (24 -48 h) |
Reduction (%) |
µ (48 -72 h) |
Reduction (%) |
control |
0.08091 |
|
0.05349 |
|
0.06631 |
|
10 |
0.07919 |
2.1 |
0.05696 |
-6.5 |
0.06487 |
2.2 |
18 |
0.07910 |
2.2 |
0.04723 |
11.7 |
0.05920 |
10.7 |
32 |
0.07939 |
1.9 |
0.3819 |
28.6 |
0.05196 |
21.6 |
56 |
0.08290 |
-2.5 |
0.02285 |
57.3 |
0.02779 |
58.1 |
100 |
0.08102 |
-0.1 |
0.02006 |
62.5 |
0.01094 |
83.5 |
Mean cell densities (x 1E+04 cells/mL)
Nominal conc. (mg/L) | Exposure time (hours) |
|||
0 | 24 | 48 | 72 | |
control | 2.4 | 10.0 | 11.5 | 40.0 |
6.3 | 2.4 | 9.0 | 13.5 | 41.3 |
12.5 | 2.4 | 9.0 | 12.3 | 39.3 |
25 | 2.4 | 9.0 | 13.0 | 36.5 |
50 | 2.4 | 7.8 | 11.8 | 38.5 |
100 |
2.4 | 7.8 | 12.3 | 37.0 |
Percentage reduction of growth rate at different time interval
Nominal conc. (mg/L) | Mean growth rate | |||||
µ (0 - 24 h) | Reduction (%) | µ (0 - 48 h) | Reduction (%) | µ (0 - 72 h) | Reduction (%) | |
control | 1.427 | 0.783 | 0.938 | |||
6.3 | 1.322 | 7.36 | 0.864 | -10.34 | 0.948 | -1.07 |
12.5 | 1.322 | 7.36 | 0.817 | -4.34 | 0.932 | 0.64 |
25 | 1.322 | 7.36 | 0.845 | -7.92 | 0.907 | 3.30 |
50 | 1.179 | 17.38 | 0.796 | -1.66 | 0.925 | 1.39 |
100 | 1.179 | 17.38 | 0.817 | -4.34 | 0.912 | 2.77 |
Description of key information
The 72-hour EC50 (growth rate) of FBSEE diol to Pseudokirchneriella subcapitata was beyond the range tested (nominal concentration of 100 mg/L). The corresponding 72-hour EC10 (growth rate) was 19 mg/L. The test was conducted per OECD TG 201.
Key value for chemical safety assessment
Additional information
In the key study, the toxicity of FBSEE diol to the green algae, Pseudokirchneriella subcapitata, was assessed in a 72-hour toxicity test conducted according to the OECD 201 method. An exponential growth was observed during the entire period of exposure in the control vessel and the validity criteria were met. Nominal concentrations were confirmed by analytical measurement (98-110%). The 72-hour ErC50 of FBSEE diol to Pseudokirchneriella subcapitata for growth rate was beyond the range tested (nominal concentration of 100 mg/L). The corresponding 72-hour NOEC (growth rate) was 10 mg/L and the 72-hour ErC10 was 19 mg/L (95% CI: 13-28 mg/L). The study was performed in accordance with internationally-accepted test guidelines under GLP. The study is deemed reliable without restriction and suitable for use in Risk Assessment, Classification & Labeling, and PBT Analysis
FBSEE diol will be rapidly converted to FBSEE diacid (see section 5.2.1). In a supporting study the toxicity of FBSEE diacid to the green algae, Pseudokirchneriella subcapitata, was assessed in a 72-hour toxicity test conducted according to the OECD 201 method. An exponential growth was observed during the entire period of exposure in the control vessel and the validity criteria were met. The 72-hour EC50 and EC10 of FBSEE diacid to Pseudokirchneriella subcapitata for growth rate were beyond the range tested (nominal concentration of 100 mg/L). The study followed an international standard method but was not GLP compliant. The results are for a degradation product rather than the parent material. Therefore the study is deemed reliable with restrictions.
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