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EC number: 264-497-8 | CAS number: 63817-45-8
- 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
Short-term toxicity to aquatic invertebrates
Administrative data
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2018-05-07 to 2018-05-09
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 018
- Report date:
- 2018
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- 1-ethyl-2-[1,2,3,4-tetrahydro-1-(2-hydroxyethyl)-2,2,4-trimethyl-6-quinolyl]benz[cd]indolium chloride
- EC Number:
- 264-497-8
- EC Name:
- 1-ethyl-2-[1,2,3,4-tetrahydro-1-(2-hydroxyethyl)-2,2,4-trimethyl-6-quinolyl]benz[cd]indolium chloride
- Cas Number:
- 63817-45-8
- Molecular formula:
- C27H31N2O.Cl
- IUPAC Name:
- 1-ethyl-2-[1-(2-hydroxyethyl)-2,2,4-trimethyl-1,2,3,4-tetrahydroquinolin-6-yl]benzo[cd]indolium chloride
- Test material form:
- solid: particulate/powder
Constituent 1
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- Determination of the test item
All concentration levels and the control were analytically verified via HPLC-DAD in the fresh media at the start of exposure (0 hours) and in the old media at the end of the exposure (48 hours).
The method was validated prior to this study according to SANCO 3029/99 rev.4 (2000).
Sampling for the analytical monitoring
At the start of the exposure (0 hours), samples of the fresh media (control and limit concentration) were taken after preparation of the limit concentration and analyzed.
At the end of the exposure (48 hours), samples of the old media (control and limit concentration) were taken directly from the test vessels.
Criteria for the analytical monitoring (target)
Recoveries of the test item should be within ± 20% of the nominal or initially measured concentrations.
Test solutions
- Vehicle:
- no
- Details on test solutions:
- Preparation of the test item solution
A stock solution with a nominal test item concentration of 15.0 mg/L was freshly prepared prior to test start with dilution water and treated with ultrasound for 10 minutes at room temperature. The test item solution was checked via laser beam (Tyndall effect) for undissolved test item. Since no Tyndall effect was observed, no undissolved test item was present in the stock solution. All tested concentration levels were visually clear throughout the exposure period.
Test concentrations
5 test item concentrations in a geometric series with a separation factor of 2.2, prepared by dilution of the stock solution 15.0 mg/L with dilution water, were tested as follows:
0.640 - 1.41 - 3.10 - 6.82 - 15.0 mg/L
The test item concentrations were based on the results of a non-GLP preliminary range finding test.
Control
Dilution water without test item incubated under the same conditions as the test group.
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Test system
Daphnia magna STRAUS (Clone 5).
Reason for the selection of the test system
Daphnia magna is the preferred species in accordance with the test guideline and is bred at the test facility.
Origin
Institut für Wasser-, Boden- und Lufthygiene (WaBoLu), 14195 Berlin, Germany
Breeder
Noack Laboratorien GmbH, Käthe-Paulus-Str. 1, 31157 Sarstedt, Germany
Culture
In glass vessels (2 - 3 L capacity) with approximately 1.8 L culture medium, at 20 +/- 2 °C, in an incubator, 16 hours illumination, light intensity of max. 1500 lx
Culture medium
Elendt M4, according to OECD 202, Annex 3 (2004) is used.
Composition of the Culture Medium Elendt M4 according to OECD 202, Annex 3 (2004)
Component Concentration [mg/L]
CaCl2 x 2 H2O 294
MgSO4 x 7 H2O 123
KCl 5.80
NaHCO3 64.8
Na2SiO3 x 5 H2O 7.47
NaNO3 0.274
KH2PO4 0.143
K2HPO4 0.184
Na2EDTA x 2 H2O 2.50
FeSO4 x 7 H2O 0.996
H3BO3 2.86
MnCl2 x 4 H2O 0.361
LiCl 0.306
SrCl2 x 6 H2O 0.152
RbCl 0.0710
NaBr 0.0160
Na2MoO4 x 2 H2O 0.0615
CuCl x 2 H2O 0.0168
ZnCl2 0.0130
CoCl2 x 6 H2O 0.0100
KI 0.00325
Na2SeO3 0.00219
NH4VO3 0.000575
Thiaminhydrochloride 0.075
Cyanocobalamin 0.0010
Biotin 0.00075
pH 8.2 +/- 0.8
Feeding of the culture stocks
The daphnids were fed at least 5 times per week ad libitum with a mix of unicellular green algae, e.g. Pseudokirchneriella subcapitata and Desmodesmus subspicatus. The algae were cultured at the test facility.
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
Test conditions
- Hardness:
- see any other informations on matrerial and methods incl. tables
- Test temperature:
- see any other informations on matrerial and methods incl. tables
- pH:
- see any other informations on matrerial and methods incl. tables
- Dissolved oxygen:
- see any other informations on matrerial and methods incl. tables
- Conductivity:
- see any other informations on matrerial and methods incl. tables
- Details on test conditions:
- Test vessels
Glass beakers (4 (ID) x 7 (H) cm), 50 mL capacity, loosely covered with watch glasses
Test volume
20 mL
Dilution water
Same composition as the culture medium
Number of daphnids and replicates
20 daphnids, divided into 4 replicates, each with 5 daphnids, were used for the limit concentration and control.
Age of the daphnids at the start of the exposure
Less than 24 hours old daphnids from a healthy stock were used
for the study. Juvenile daphnids were removed from the culture vessels at the latest 24 hours before the start of the exposure and discarded. The juveniles born within the following period of max. 24 hours preceding the exposure were used for the test. No first brood progeny was used for the test.
Acclimatization
Acclimatization of the daphnids was not necessary, because the composition of the dilution water was equivalent to the culture medium.
Application
20 g test solution per replicate was weighed out into each test vessel. This corresponds to 20 mL per test vessel. The daphnids were inserted with a small amount of dilution water by a pipette.
Test temperature (target)
18 - 22 °C, constant within ± 1 °C
Illumination (target)
Diffuse light, light intensity of max. 1500 lx
Photoperiod (target)
16/8 hours light/dark cycle
Feeding
The daphnids were not fed during the study. - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 24 h
- Dose descriptor:
- EC10
- Effect conc.:
- 0.749 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: CI: <0.640 - 1.12
- Duration:
- 48 h
- Dose descriptor:
- EC10
- Effect conc.:
- 1.25 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: CI: 0.672 - 2.66
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 2.15 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: CI: 1.37 - 3.19
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 1.41 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: CI: 0.727 - 2.75
- Duration:
- 24 h
- Dose descriptor:
- EC100
- Effect conc.:
- 15 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC100
- Effect conc.:
- 3.1 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Results with reference substance (positive control):
- Test of the Reference Item
The percentage of immobility for the reference item potassium dichromate (SIGMA-ALDRICH, batch number MKBV0900V, purity 99.0%, CAS RN 7778-50-9) was determined after 24 hours from 2018 05-03 to 2018-05-04.
EC50-Value (with 95% Confidence Limits) of the Reference Item Potassium dichromate
based on nominal concentrations mg/L, (0 - 24 hours)
Current Study Valid Range
EC50 2.07 mg/L
0.6 - 2.4 mg/L, acc. to AQS P 9/2 (02/2000); clone 5
0.6 - 2.1 mg/L, acc. to OECD 202 (2004); clone A
95% confidence limits 1.00 - 4.00 mg/L
- Reported statistics and error estimates:
- Methods of evaluation
The EC100-values after 24 and 48 hours were empirically derived from the observation data. The effect levels (EC10 / 50 / 100) are given based on the nominal concentrations, since the measured test item concentrations were within ± 20% of the nominal concentrations.
EC-values and statistical analyses
The EC10- and EC50-values (after 24 and 48 hours of exposure) were calculated by sigmoidal dose-response regression with the software GraphPad Prism. The respective 95% confidence limits were calculated from the standard error and the t distribution. In case that the confidence limits could not be calculated by the software, the respective confidence limits were empirically derived from the observation data. The concentration-effect relationships are shown graphically.
An EC50 value for the reference item was calculated accordingly. The respective 95% confidence limits were empirically derived from the observation data as follows: The highest concentration level without any effect (EC0) and the lowest concentration level causing 100% immobilization (EC100) were used as 95% confidence limits, since the calculated values were classified as ambiguous by the software.
All calculations were carried out from the best-fit values with the software GraphPad Prism.
Software
All data were computer-processed and rounded for presentation. Consequently, minor variations may occur from the original figures if manual calculations based on the original figures are made subsequently. Calculations were made using the following software:
- GraphPad Prism, GRAPHPAD SOFTWARE, INC.
- Excel, MICROSOFT CORPORATION
Any other information on results incl. tables
Measured Exposure Concentrations during the Definitive Test
The concentrations of the test item Basic Blue 147 Chloride were analytically verified via HPLC-DAD in the fresh media at the start of the exposure (0 hours) and in the old media at the end of the exposure (48 hours) in all tested concentration levels and in the control.
The measured concentrations of the test item at the start of the exposure (0 hours) were in the range of 97 to 105% of the nominal values. At the end of the exposure period (48 hours), the measured concentrations were within the range of 92 to 103% of the nominal values.
The measured concentrations of the test item were within ± 20% of the nominal concentrations. This indicates that the test item concentrations were successfully maintained for the duration of the test.
Measured Concentrations and Percent of the Nominal Concentration of the Test Item Basic Blue 147 Chloride during the Definitive Test
Sampling date |
Start of the exposure, |
End of the Exposure, |
||
Nominal test item concentration [mg/L] |
Basic Blue147Chloride |
|||
Meas. conc. [mg/L] |
% |
Meas. conc. [mg/L] |
% |
|
15.0 |
14.8 |
99 |
15.4 |
103 |
6.82 |
6.64 |
97 |
6.66 |
98 |
3.10 |
3.01 |
97 |
2.99 |
96 |
1.41 |
1.48 |
105 |
1.38 |
98 |
0.640 |
0.675 |
105 |
0.590 |
92 |
Control |
< LOQ |
< LOQ |
Meas. conc. = measured concentration of the test item, mean value of two injections, dilution factors taken into account
% = percentage of the nominal concentration of the test item
LOQ = limit of quantification (0.1 mg test item/L)
Preliminary Range Finding Test (non-GLP)
A non-GLP preliminary range finding test was conducted at the test facility under static conditions over a period of 48 hours with three nominal test item concentrations of 1, 10 and 100 mg/L prepared with dilution water. The preliminary range finding test was conducted under diffuse light conditions (light intensity of max. 1500 lx, 16/8 hours light/dark cycle).
The test item solutions were visually clear and concentration related purple coloured.
In the range finding test, two replicates per concentration level and control, each with five daphnids, were tested.
Immobilization Rates in the non-GLP Preliminary Range Finding Test
(n = 10, divided into 2 replicates with 5 daphnids each)
Nominal test item concentration [mg/L] |
IMMOBILIZATION [%] |
||||||||||||
24 hours |
48 hours |
||||||||||||
Replicates |
Replicates |
||||||||||||
1 |
2 |
MV |
1 |
2 |
MV |
||||||||
100 |
100 |
100 |
100 |
100 |
100 |
100 |
|||||||
10 |
100 |
100 |
100 |
100 |
100 |
100 |
|||||||
1 |
0 |
0 |
0 |
0 |
0 |
0 |
|||||||
Control |
0 |
0 |
0 |
0 |
0 |
0 |
MeasuredConcentrations ofBasicBlue 147 Chlorideduring the non-GLPPreliminary Range Finding TesT
Analytical system: HPLC-DAD
Sampling |
Start of the exposure, 0 hours |
End of the Exposure, 48 hours |
||
Nominal test item concentration [mg/L] |
BasicBlue 147 Chloride |
|||
Measured concentration [mg/L] |
% |
Measured concentration [mg/L] |
% |
|
100 |
118 |
118 |
114 |
114 |
10 |
11.1 |
111 |
10.9 |
109 |
1 |
1.08 |
108 |
1.04 |
104 |
Control |
< LCL |
< LCL |
% = percent of the nominal concentration of the test item
LCL = lowest calibration level (0.05 mg/L of the test item)
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- Based on the nominal concentrations of the test item Basic Blue 147 Chloride, the 48-hours EC50 for Daphnia magna was 1.41 mg/L (95% confidence limits: 0.727 – 2.75 mg/L).
- Executive summary:
In the acute immobilization test with Daphnia magna(STRAUS), the effects of the test item Basic Blue 147 Chloride were determined at the test facility according to OECD 202 (2004) from 2018-05-07 to 2018-05-09.
The study was conducted under static conditions over a period of 48 hours with five nominal test item concentrations in a geometric series with a separation factor of 2.2. All tested concentration levels were visually clear and concentration-depended blue coloured throughout the exposure period.
Twenty daphnids (divided into 4 replicates with 5 daphnids each) were exposed to each concentration leveland the control.
The concentrations of the test item Basic Blue 147 Chloride were analytically verified via HPLC-DAD in the fresh media at the start of the exposure (0 hours) and in the old media at the end of the exposure (48 hours) in all tested concentration levels and in the control.
The measured concentrations of the test item at the start of the exposure (0 hours) were in the range of 97 to 105% of the nominal values. At the end of the exposure period (48 hours), the measured concentrations were within the range of 92 to 103% of the nominal values.
The measured concentrations of the test item were within ± 20% of the nominal concentrations. This indicates that the test item concentrations were successfully maintained for the duration of the test. Therefore, all effect concentrations are based on the nominal concentrations of the test item Basic Blue 147 Chloride.
The validity criteria of the test guideline were fulfilled.
EC10-, EC50- (with 95% Confidence Limits) and EC100-Values
(based on the nominal concentrations of the test item)
Effect concentrations
Test duration
[hours]
BasicBlue 147Chloride
Nominal test item concentration
[mg/L]
EC10
(with 95% confidence limits)
24
0.749
(95% Cl:≤0.640 – 1.12)
48
1.25
(95% Cl: 0.672 – 2.66)
EC50
(with 95% confidence limits)
24
2.15
(95% Cl: 1.37 – 3.19)
48
1.41
(95% Cl: 0.727 – 2.75)
EC100
24
15.0
48
3.10
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