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EC number: 457-900-5 | CAS number: -
- 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:
- 04 - 06 Aug 2015
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP - Guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 015
- Report date:
- 2015
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- Landesamt für Umwelt, Wasserwirtschaft und Gewerbeaufsicht, Mainz, Germany
Test material
Reference
- Name:
- Unnamed
- Type:
- Constituent
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- - Name of test material (as cited in study report): PM-5927
- Substance type: Whitish/Crystalline powder
- Physical state: solid
- Lot/batch No.: 14-121
- Expiration date of the lot/batch: 01 June 2016
- Storage condition of test material: Room Temperature (20 ± 5 °C); Keep away from light
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- At the beginning and at the end of the test, the content of the test item in the test solutions was determined using HPLC-determination by measuring Sulfonium, tris(4-chlorophenyl)-(cation) and 5-benzoyl-4-hydroxy-2-methoxybenzene-sulfonic acid (anion).
Test solutions
- Vehicle:
- no
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: water flea
- Source: originally from Umweltbundesamt Berlin, Germany; in-house breeding since 27 Sep 2007
- Age at study initiation (mean and range, SD): < 24 hours
- Method of breeding: Daphnia magna is bred in the LAUS GmbH throughout the year. The animals are kept for the use in toxicity tests. They multiply by parthenogenesis, thus being genetically identical. The husbandry is performed similar to the method described in EN ISO 6341. Vessels: preserving glasses, nominal volume 2 L; Medium: M4-Medium (recipe of ELENDT); Medium renewal twice a week; Photo period: 16/8 hours, using neon tubes; Temperature 20 ± 2 °C
- Feeding during test: none
- Food type: unicellular green algae (Desmodesmus subspicatus)
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
Test conditions
- Test temperature:
- 19.8 - 21.0 °C
- pH:
- 7.5 - 7.8
- Dissolved oxygen:
- 8.5 - 8.8 mg O2/L
- Nominal and measured concentrations:
- control, 10, 18, 32, 54, and 100 mg/L (nominal)
- Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Material, size, headspace, fill volume: Beakers, glass, nominal volume 50 mL
- Aeration: After preparation, the dilution water was aerated
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Deionised water with an enrichment of certain minerals (according to guidelines)
OTHER TEST CONDITIONS
- Adjustment of pH: yes, to 7.9
- Light intensity: diffuse lighting
EFFECT PARAMETERS MEASURED (with observation intervals if applicable): 24 and 48 hours, the immobilised Daphnia were counted
TEST CONCENTRATIONS
- Spacing factor for test concentrations: ca. 1.8
- Range finding study:
Test concentrations: 1, 10, and 100 mg/L
- Results used to determine the conditions for the definitive study: At the concentration 100 mg/L, 100 % immobilization was observed. In the lower concentrated treatments none of the Daphnia were immobilized. - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 19 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 10 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- LOEC
- Effect conc.:
- 18 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Results with reference substance (positive control):
- Potassium dichromate K2Cr2O7 was used as positive control in a current reference study. The 24h-EC50 value was determined as 1.6 mg/L, lying within the demanded range of 0.6 – 1.7 mg/L.
- Reported statistics and error estimates:
- Calculation of results was performed with the help of validated software (Microsoft Excel®). The estimation of the biological data was accomplished using the software ToxRat® Professional, version 3.1.
Any other information on results incl. tables
Analytical Determinations:
The determined concentrations of the cation at the start and the end of the test were in the range of 97 % - 110 % of the nominal concentration. The determined concentrations of the anion at the start and the end of the test were in the range of 98 % - 109 % of the nominal concentration. Therefore, the determination of the biological results was based on the nominal concentration.
Table 1: Measured concentrations (cation)
Nominal Concentration test item |
Measured Concentration in mg/L (t = 0 h) |
Measured Concentration in mg/L (t = 48 h) |
% of Nominal Concentration (t = 0h) |
% of Nominal Concentration (t = 48h) |
mg/L |
mg/L |
mg/L |
mg/L |
mg/L |
Blank control |
n.d. |
n.d. |
n.d. |
n.d. |
10 |
9.99 |
10.74 |
100% |
107% |
18 |
17.52 |
18.95 |
97% |
105% |
32 |
32.61 |
35.26 |
102% |
110% |
54 |
54.31 |
58.59 |
101% |
109% |
100 |
100.87 |
108.66 |
101% |
109% |
Table 2: Measured concentrations (anion)
Nominal Concentration test item |
Measured Concentration in mg/L (t = 0 h) |
Measured Concentration in mg/L (t = 48 h) |
% of Nominal Concentration (t = 0h) |
% of Nominal Concentration (t = 48h) |
mg/L |
mg/L |
mg/L |
mg/L |
mg/L |
Blank control |
n.d. |
n.d. |
n.d. |
n.d. |
10 |
10.01 |
10.70 |
100% |
107% |
18 |
17.57 |
18.84 |
98% |
105% |
32 |
32.39 |
35.03 |
101% |
109% |
54 |
53.69 |
57.93 |
99% |
107% |
100 |
100.03 |
107.72 |
100% |
108% |
Biological Findings:
Table 3: Immobility
Nominal Concentration in mg/L |
Immobility 24 hours |
Immobility 48 hours |
||||||||
absolute |
in % |
absolute |
in % |
|||||||
Blank control |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
10 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
18 |
0 |
0 |
0 |
0 |
0 |
1 |
2 |
1 |
2 |
30 |
32 |
3 |
1 |
1 |
4 |
45 |
5 |
5 |
5 |
5 |
100 |
54 |
5 |
5 |
4 |
5 |
95 |
5 |
5 |
5 |
5 |
100 |
100 |
5 |
5 |
5 |
5 |
100 |
5 |
5 |
5 |
5 |
100 |
Validity:
- The 24h-EC50 of K2Cr2O7 should lie between 0.6 and 1.7 mg/L. The 24h-EC50 of K2Cr2O7 was determined as 1.6 mg/L in a separate GLP study.
- Immobilisation in the controls may not exceed 10 %. Immobilisation in the controls was 0 %.
- The concentration of dissolved oxygen at the end of the test must be at least 3 mg/L. The lowest concentration of dissolved oxygen at the end of the test was 8.5 mg/L.
- The pH-value in the test solutions should not vary by more than 1.5 units during the test. The highest variation was 0.3 units.
Applicant's summary and conclusion
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.