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EC number: 266-867-4 | CAS number: 67674-28-6
- 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:
- from 2018-04-23 to 2018-04-26, with the definitive exposure phase from 2018-04-24 to 2018-04-26
- 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:
- Sodium m-[[4-[[p-[bis(2-hydroxyethyl)amino]phenyl]azo]-1-naphthyl]azo]benzenesulphonate
- EC Number:
- 266-867-4
- EC Name:
- Sodium m-[[4-[[p-[bis(2-hydroxyethyl)amino]phenyl]azo]-1-naphthyl]azo]benzenesulphonate
- Cas Number:
- 67674-28-6
- Molecular formula:
- C26H25N5O5S.Na
- IUPAC Name:
- sodium m-[[4-[[p-[bis(2-hydroxyethyl)amino]phenyl]azo]-1-naphthyl]azo]benzenesulphonate
- Test material form:
- solid: particulate/powder
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 were taken from the freshly prepared concentration levels and the control for analysis.
At the end of the exposure (48 hours), samples for the analyses of the old media were taken from test replicates containing daphnids.
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:
- Stock solution
A stock solution of 100 mg test item/L was prepared once 24 ± 1 hour prior to the start of the exposure. 100 mg/L of the test item were weighed out. The test item was applied onto a glass slide. The glass slide with the test item was inserted into a glass bottle with 1000 mL of the dilution water. The test item solution was stirred for 24 ± 1 hours (1100 rpm, room temperature) with a magnetic stirrer. Undissolved particles were removed by membrane filtration (membrane filter 0.45 µm, RC, Macherey-Nagel). The filter was saturated in order to avoid adsorption during the filtration. The first 25 mL of the filtrate were discarded. The filtration was interrupted for 15 minutes to allow adsorption and saturation of the filter material with dissolved test item. Thereafter, the filtration was continued. The next 25 mL were discarded. The following filtrate, i.e. the saturated solution, was used as the highest concentration level and as the stock solution for the preparation of further concentration. During filtration, the filter was always kept covered.
The stock solution was checked via laser beam (Tyndall effect) for undissolved test item. No Tyndall-effect was detected and no undissolved test item was present during the test.
Test concentrations
5 test item concentrations in a geometric series with a separation factor of √10, prepared by dilution of the saturated solution with dilution water, were tested as follows:
1.00 - 3.16 - 10.0 - 31.6 - 100% of the saturated solution, prepared with 100 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 groups
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:
- Dilution water
0 hours:Total hardness [mg CaCO3/L]: 267 - Test temperature:
- 18 - 22°C, constant within ± 1°C
20 °C - pH:
- Water Quality Parameters in fresh Media at the Start of the Exposure (0 hours)
(measured in one additional replicate (without daphnids) per concentration level and control)
Geometric mean
measured test item
concentration
[µg/L] pH-value Dissolved O2 concentration [mg/L]
1058 7.83 8.50
344 7.77 8.97
81.1 7.79 9.18
26.0 7.76 9.18
10.0 7.77 9.13
Control 7.74 9.09
Water Quality Parameters in old Media at the End of the Exposure (48 hours)
(measured in one replicate (containing daphnids) per concentration level and control)
Geometric mean
measured test item
concentration
[µg/L] pH-value Dissolved O2 concentration [mg/L] Replicate number
1058 7.56 8.11 4
344 7.58 8.21 4
81.1 7.64 8.24 4
26.0 7.67 8.25 4
10.0 7.67 8.30 4
Control 7.79 8.34 4
Water Quality Parameters of the Dilution Water at the Start of the Exposure (0 hours)
Dilution water
dated: pH-value Dissolved O2 concentration [mg/L] Temperature [°C] Conductivity [µS/cm] Total hardness [mg CaCO3/L]
2018-04-24 8.39 9.29 19.3 624 267 - Dissolved oxygen:
- see above
- Conductivity:
- See above
- Nominal and measured concentrations:
- nominal concentrations: 1.00 - 3.16 - 10.0 - 31.6 - 100% of the saturated solution
geometric mean measured concentrations: 10.0 – 26.0 – 81.1 – 344 – 1058 µg/L - 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:
- other: EC10/50/100
- Effect conc.:
- > 1 058 µg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- other: EC10750/100
- Effect conc.:
- > 1 058 µg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Results with reference substance (positive control):
- 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 04-10 to 2018-04-11. For results of the most recent of the monthly performed reference tests, see Table 6.
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 1.89 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 EC10 / 50 / 100-values after 24 and 48 hours were empirically derived from the observation data.
EC-values and statistical analyses for thereference item
An EC50 value was calculated for the reference item by sigmoidal dose-response regression from the best-fit values with the software
GraphPad Prism. The respective 95 % confidence limits for the EC50 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 calculation was not possible by the software.
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.
- SigmaPlot, SPSS INC.
- Excel, MICROSOFT CORPORATION
Any other information on results incl. tables
Measured Exposure Concentrations during the Definitive Test
The concentrations of the test item Acid Red 299 were analytically verified via HPLC-DAD in the fresh media at the start of the exposure (0 hours) and in 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 < LOQ to 1220 µg/L. At the end of the exposure period (48 hours), the measured concentrations were within the range of < LOQ to 83% of the initial concentrations. The geometric mean measured concentrations are: 10.0 – 26.0 – 81.1 – 344 – 1058 µg/L.
The measured test item concentrations were not within±20% of the initial concentrations of the test item over the test period.
Table5: Measured Concentrations and Percent of Initial Measured Concentration of the Test ItemAcid Red299during the Definitive Test
Sampling date |
Start of the exposure, |
End of the Exposure, |
Geometric mean measured test itemconcentration1) |
|
Dilution level of the saturated solution [%] |
Acid Red299 |
|||
Meas. conc. [µg/L] |
Meas. conc. [µg/L] |
% |
||
100 |
1220 |
917 |
75 |
1058 |
31.6 |
379 |
312 |
83 |
344 |
10.0 |
90.9 |
72.3 |
80 |
81.1 |
3.16 |
31.0 |
21.8 |
70 |
26.0 |
1.00 |
< LOQ |
< LOQ |
10.0 |
|
Control |
< LOQ |
< LOQ |
|
Meas. conc. = measured concentration of the test item, mean value of two injections, dilution factor taken into account
% = percentage of the initially measured concentration of the test item
LOQ = limit of quantification (20 µg test item/L)
1) =
If the measured concentration was < LOQ, 1/2 LOQ (10 µg test item/L) was
used for the calculation of
thegeometric
mean measured concentrations.
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 four nominal test item concentrations of 0.1, 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 solution was prepared in the same way as in the definitive test. The Tyndall effect was negative for the saturated solution after filtration of undissolved material. The test item solutions were visually clear and concentration related pink to red coloured.
In the range finding test, two replicates per concentration level and control, each with ten daphnids, were tested.
Immobilization Rates in the non-GLP Preliminary Range Finding Test
(n = 20, 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 |
60 |
80 |
70 |
60 |
80 |
70 |
|||||||
10 |
20 |
20 |
20 |
20 |
20 |
20 |
|||||||
1 |
0 |
0 |
0 |
0 |
20 |
10 |
|||||||
0.1 |
0 |
20 |
10 |
0 |
20 |
10 |
|||||||
Control |
0 |
20 |
10 |
0 |
20 |
10 |
MeasuredConcentrations ofAcidRed 299during the non-GLPPreliminary Range Finding Test
Analytical system: HPLC-DAD
Sampling date |
2018-02-27 Start of the exposure, 0 hours |
2018-03-01 End of the Exposure, 48 hours |
||
Nominal test item concentration [mg/L] |
AcidRed 299 |
|||
Measured concentration [mg/L] |
% |
Measured concentration [mg/L] |
% |
|
100 |
0.889 |
1 |
0.800 |
1 |
10 |
0.0793 |
1 |
0.0785 |
1 |
1 |
< LCL |
< LCL |
||
0.1 |
< LCL |
< LCL |
||
Control |
< LCL |
< LCL |
% = percent of the nominal concentration of the test item
LCL = lowest calibration Level (10µg/L of the test item)
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- Based on the geometric mean measured concentrations of the test item Acid Red 299, the 48-hours EC50 for Daphnia magna was > 1058 µg/L. No effects on Daphnia magna STRAUS were observed up to the limit of solubility in the test medium.
- Executive summary:
In the acute immobilization test with Daphnia magna (STRAUS), the effects of the test item Acid Red 299 were determined at the test facility according to OECD 202 (2004) from 2018-04-23 to 2018-04-26, with the definitive exposure phase from 2018-04-24 to 2018-04-26.
The study was conducted under static conditions over a period of 48 hours with a saturated solution with a nominal loading of100 mg/Lof the test item Acid Red 299 and further four dilution levels in a geometric series with a separation factor of √10 (1 to 31.6% of the saturated solution). All tested concentration levels were visually clear and concentration-depended pink coloured throughout theexposure period.
Twenty daphnids (divided into 4 replicates with 5 daphnids each) were exposed to each dilution leveland the control.
The concentrations of the test item Acid Red 299 were analytically verified via HPLC-DAD in the fresh media at the start of the exposure (0 hours) and in 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 < LOQ to 1220 µg/L. At the end of the exposure period (48 hours), the measured concentrations were within the range of < LOQ to 83% of the initial concentrations. The geometric mean measured concentrations are: 10.0 – 26.0 – 81.1 – 344 – 1058 µg/L.
The measured test item concentrations were not within ± 20% of the initial concentrations of the test item over the test period. Therefore, the effect concentrations given are based on the geometric mean measured concentrations of the test item Acid Red 299.
The validity criteria of the test guideline were fulfilled.
EC10-, EC50-and EC100-Values
(based on the geometric mean measured concentrations of the test item)
Effect levels
Test duration
[hours]
AcidRed 299
Geometric mean measured test item concentration
[µg/L]
EC10
(with 95% confidence limits)
24
> 1058
48
> 1058
EC50
(with 95% confidence limits)
24
> 1058
48
> 1058
EC100
24
> 1058
48
> 1058
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