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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 297-025-4 | CAS number: 93281-13-1
- 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
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- December from 05 to 07, 1990
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- test procedure in accordance with generally accepted scientific standards and described in sufficient detail
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Version / remarks:
- adopted April 4th, 1984.
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- Analytical measurements of the test substance were performed in samples of test media of the nominal test concentrations 31.3, 125.0 and 500.0 mg test substance/l and control at the start and the end of the test by sampling freshly prepared test media and media, which were incubated during test duration under the same conditions as in the test itself (but without Daphnia).
All samples are kept stored at -20 °C to enable additional analyses. After delivery of the final test report all samples will be discarded. - Details on test solutions:
- A stock solution was prepared by dissolving the test substance in test water (0.5 g/l). The stock solution was diluted in a series of sequential dilutions with test water to prepare the nominal concentrations.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Daphnia magna.
- Strain/clone: clone of Daphnia magna Straus.
- Source: bred in the testing laboratory.
- Age at the start of the test: 6 - 24 hours old.
ACCLIMATION
- Acclimation conditions: the parental Daphnia were maintained in the same reconstituted water as in the test for at least 24 hours prior to the start of the test. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Test temperature:
- 18.1 - 19.6 °C
- pH:
- 7.6 - 8.1
- Dissolved oxygen:
- ≥ 8 mg/l
- Nominal and measured concentrations:
- Nominal: 31.3, 62.5, 125, 250 and 500 mg/l
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 100 ml - glass beaker.
- Fill volume: 50 ml.
- No. of organisms per vessel: groups of 5 animals.
- No. of organisms per concentration: 20.
- No. of vessels per concentration: 4.
- No. of vessels per control: 4.
TEST MEDIUM
- Preparation of test medium: reconstituted water aerated to saturation was used in the test (according to the EEC Directive). In deionized water with a conductivity lower than 0.1 μs/cm analytical grade salts were dissolved to following nominal concentrations: 294 mg/l of CaCl2.2H2O, 123 mg/l of MgSO4.7H2O, 65 mg/l of NaHCO3, 5.8 mg/l of KCl.
- Hardness: 2.5 mmol/l as CaCO3.
- Alkalinity: 0.8 mmol/l.
- Ca : Mg ratio: 4 : 1
- Na : K ratio: 10 : 1
OTHER TEST CONDITIONS
- Photoperiod: 16 hrs light / 8 hrs darkness.
- Light intensity: about 200-600 Lux.
EFFECT PARAMETERS MEASURED
The immobility or mortality of the Daphnia was determined by visual control after 24 and 48 hours: those animals not able to swim within 15 seconds after gentle agitation of the test beaker are considered to be immobile, respectively dead.
The 48-hour EC 10, -50 and -90 and their 95 %-confidence limits were calculated by the Probit Analysis. After 24 hours test duration only the EC 50 could be calculated by the Moving Average Interpolation.
PARAMETERS MEASURED
At the start of the test, the pH-values and the dissolved oxygen concentrations were determined in the control and in the highest concentration tested, at the end of the test these parameters in all test concentrations and control. Water temperature was measured in one control beaker at the start and the end of the test.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2.
- Range finding study: the test concentrations were based on the results of a range-finding test which was though not performed in compliance with GLP. - Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 64.9 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other:
- Remarks:
- 95 % CL: 53.8 - 78.3 mg/l.
- Details on results:
- The 24-hour EC50 of the test substance was calculated to be 240.6 mg test substance/l with 95 % confidence limits from 204.5 to 283.0 mg test substance/l.
After 48 hours test duration the toxicity of the test substance has highly increased. The 48-hour EC50 was calculated to be 64.9 mg test substance/l with 95 % confidence limits from 53.8 to 78.3 mg test substance/l. The calculated 48-hour EC10 was 35.5 mg test substance/l (95 % confidence limits: 26.4 47.8 mg/l), the 48-hour EC90 amounted to 118.8 mg test substance/l (95 % confidence limits: 89.0 - 158.5 mg/l). The 48-hour EC100 was determined to be 250 mg test substance/l.
In the control no immobility or mortality of the test animals was observed.
MEASURED CONCENTRATION
The test substance concentrations in the analysed test media were in the range of 95.8 - 112.3 % of the nominal values during test duration. The test substance was sufficiently stable under test conditions. Therefore, all reported results are related to the nominal concentrations of the test substance. - Validity criteria fulfilled:
- yes
- Remarks:
- mortality of the control did not exceed 10 % at the end of the test, dissolved oxygen concentration was more than 60 % of air saturation value
- Conclusions:
- EC50 (48h): 64.9 mg/l (nominal)
- Executive summary:
The acute toxicity of test item to Daphnia magna was determined in a 48-hour static test according to the OECD Guideline for Testing of Chemicals, Section 2, No. 202, adopted April 04, 1984 and the EEC Directive 84/449, L 251, Part C 2.
The nominal concentrations tested were 31.3, 62.5, 125, 250 and 500 mg test substance/l and a control (test water without any additions).
The 24-hour EC50 of the test substance was calculated to be 240.6 mg test substance/l with 95 % confidence limits from 204.5 to 283.0 mg test substance/l. After 48 hours test duration the toxicity of the test substance has highly increased. The 48-hour EC50 was calculated to be 64.9 mg test substance/l with 95 % confidence limits from 53.8 to 78.3 mg test substance/l. The calculated 48-hour EC10 was 35.5 mg test substance/l (95 % confidence limits: 26.4 47.8 mg/l), the 48-hour EC90 amounted to 118.8 mg test substance/l (95 % confidence limits: 89.0 - 158.5 mg/l). The 48-hour EC100 was determined to be 250 mg test substance/l.
In the control no immobility or mortality of the test animals was observed.
The test substance concentrations in the analysed test media were in the range of 95.8 - 112.3 % of the nominal values during test duration. The test substance was sufficiently stable under test conditions. Therefore, all reported results are related to the nominal concentrations of the test substance.
Conclusion
EC50 (48h): 64.9 mg/l (nominal) (95 % conf. limits: 53.8 - 78.3 mg/l)
Reference
Influence of the substance on the mobility of Daphnia magna.
Nominal conc. of test substance |
No of Daphnia tested |
No of immobilized Daphnia after: | % of immobilized Daphnia after: | ||
24 h | 48 h | 24 h | 48 h | ||
Control | 20 | 0 | 0 | 0 | 0 |
31.3 mg/l | 20 | 1 | 1 | 5 | 5 |
62.5 mg/l | 20 | 1 | 10 | 5 | 50 |
125.0 mg/l | 20 | 1 | 18 | 5 | 90 |
250.0 mg/l | 20 | 15 | 20 | 75 | 100 |
500.0 mg/l | 20 | 10 | 20 | 50 | 100 |
Quality measurements (dissolved oxygen and pH) of the test media at the start and end of the acute toxicity test are presented in the table below.
Nominal conc. of test substance |
Start (0 hours) | End (0 hours) | ||
Oxygen | pH | Oxygen | pH | |
Control | 9.3 | 7.9 | 8.5 | 8.1 |
31.3 mg/l | * |
* |
8.5 | 8.0 |
62.5 mg/l | * |
* | 8.6 | 7.9 |
125.0 mg/l | * |
* | 8.5 | 7.9 |
250.0 mg/l | * | * | 8.4 | 7.9 |
500.0 mg/l | 9.3 | 7.6 | 8.0 | 7.9 |
* = not measured
Results obtained for the concentrations of test item in test medium
Nominal concentration [mg/l] | Sampling period | Conc. of test item found [mg/l]* | % of nominal |
31.3 |
B |
30.0 |
95.8 |
31.3 |
E |
32.4 |
103.4 |
125.0 |
B |
128.2 |
102.6 |
125.0 |
E |
140.0 |
112.0 |
500.0 |
B |
510.8 |
102.2 |
500.0 |
E |
561.6 |
112.3 |
Control sample |
B |
--- ** |
--- |
Control sample |
E |
--- ** |
--- |
* Mean value of a repeated test
** Counts were below lowest calibration point
B = Beginning of experiment
E = End of experiment
Description of key information
EC50 (48h): 64.9 mg/l (nominal)
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 64.9 mg/L
Additional information
The acute toxicity of test item to Daphnia magna was determined in a 48-hour static test according to the OECD Guideline 202. The nominal concentrations tested were 31.3, 62.5, 125, 250 and 500 mg test substance/l. The 24-hour EC50 of the test substance was calculated to be 240.6 mg test substance/l with 95 % confidence limits from 204.5 to 283.0 mg test substance/l. After 48 hours test duration the toxicity of the test substance has highly increased. The 48-hour EC50 was calculated to be 64.9 mg test substance/l with 95 % confidence limits from 53.8 to 78.3 mg test substance/l. The calculated 48-hour EC10 was 35.5 mg test substance/l (95 % confidence limits: 26.4 47.8 mg/l), the 48-hour EC90 amounted to 118.8 mg test substance/l (95 % confidence limits: 89.0 - 158.5 mg/l). The 48-hour EC100 was determined to be 250 mg test substance/l.
In the control no immobility or mortality of the test animals was observed. The test substance concentrations in the analysed test media were in the range of 95.8 - 112.3 % of the nominal values during test duration. The test substance was sufficiently stable under test conditions.
A second test on the substance under registration is available. The composition of the tested substance is comparable to those of the lot tested in the abovementioned experiment, however the results obtained are significantly different.
The acute toxicity of the substance to Daphnia magna was determined in a 48-hr test according to the OECD Guideline 202. 20 daphnids (divided in 4 groups of 5 daphnids each) were exposed to 5 concentrations of the substance, i.e. 0.1, 1, 10, 100 and 1000 mg/l, over a period of 48 hours. The EC50 at 24 hours resulted to be 12.9 mg/l, while at 48 hours the EC50 resulted to be 1.20 mg/l.
Also in this case, after 48 hours test duration the toxicity of the test substance has highly increased; however, the magnitude of the effects resulted to be significantly higher respect to those recorded in the key study. Based on the available information, no clear explanation can be given about the differences obtained in the toxicity impact: as mentioned, the composition of the tested substances is comparable and the testing conditions are very similar. From the mobility reading point of view, the colouration of the test item may be a discriminating; however, there are no information or indication in the test report, which may let rise a suspect of an adverse impact.
In order to clarify the potential for short-term toxicity to aquatic invertebrates, the available data on the structural analogous Similar Substance 01 have been taken into account. Similar Substance 01 shares with Direct Black 168 the same scaffold chemical structure base; the differences are considered to be not able to impact the study outcomes, thus the read across can be considered as reliable and appropriated to evaluate the endpoint. Details on read-across approach are given in the IUCLID section 13.
The toxicity of the substance to Daphnia magna was assessed in the acute immobilization test, according to the OECD Guideline 202. Twenty daphnids (divided in 4 groups of 5 daphnids each) were exposed to 9 concentrations of the substance, ranging from 10 to 1000 mg/l (in a geometric progression with a dilution factor of 1.8), over a period of 48 hours. The number of daphnids that were floated in the water surface (immobilised) were measured at 24 h and 48 h in order to calculate the EC0 and EC100. The concentration-immobilization percentage was presented in a graph and the EC50 was calculated from the graph. The substance was dissolved in the water completely and the test solutions were all homogenised. However, at the concentrations 580 mg/l and 1000 mg/l it was not possible to measure the immobilised daphnids due to black coloration of the test solutions. No immobilization in the control group was recorded, i.e. 0 % at 24 h and 48 h. The recovery rate of the measured concentration was over 100 % in all the cases; it was higher than 120 % in 3 cases (32 mg/l, 100 mg/l and 180 mg/l). The EC50 value at 48 hours was found to be 76 mg/l (nominal).
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.