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EC number: 947-946-9 | 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
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:
- 26 February 2018 to ****
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- -Purity: Unknown or Variable composition, is a Complex reaction product, or a Biological material (UVCB)
-Description: Dark Green Liquid - Analytical monitoring:
- yes
- Remarks:
- Given that the test substance is a multi-constituent substance and analytical monitoring was limited to the dithiophosphate fraction (without molybdenum) of the test substance, the results were based on nominal loading rates.
- Details on sampling:
- - Concentrations: Control, 1.0, 3.2, 10, 32, and 100 mg/L loading rate WAF
- Sampling method: Aqueous samples (10 mL) of freshly prepared test media (0 hour) and pooled expired test media (48 hours) were collected in duplicate, mixed with acetonitrile, then diluted further with Elendt M4 media:acetonitrile (1:1, v/v) as required to bring the response within the calibration range.
- Sample storage conditions before analysis: Not applicable - Vehicle:
- no
- Details on test solutions:
- The substance is a chemical substance of Unknown or Variable Composition, Complex Reaction Products and Biological Materials (UVCB) with low water solubility and as such falls into the category of a “difficult substance” as defined by the OECD Guidance Document (OECD Series on Testing and Assessment, No. 23 (2000); Guidance Document on Aquatic Toxicity Testing of Difficult Substances and Mixtures). Based on the recommendations of this guideline, the test solutions were prepared as Water Accommodated Fractions (WAFs).
At the start of the test, the test substance was weighed onto a glass slides and placed in 1000 mL of Elendt M4 test medium. The preparations were stirred for ca 23 hours at a rate such that a slight dimple was formed at the surface. After the stirring period, the preparations were allowed to settle for ca 1 hour, after which the aqueous phase was removed by careful mid-depth siphoning to give the 1.0, 3.2, 10, 32 and 100 mg/L loading rate WAF. A control group was prepared in the same manner without the addition of test substance. - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- - Test organism: juvenile Daphnia magna (Straus), less than 24 hours old
- Source: parental laboratory cultures, held and maintained at the test facility
- Age of parental stock: less than 24 hours old
- Food type: cultures fed daily with a concentrated suspension of Chlorella vulgaris
- Feeding during test: none - Test type:
- static
- Water media type:
- other: Elendt M4 medium
- Total exposure duration:
- 48 h
- Hardness:
- Not specified.
- Test temperature:
- 20 ± 2ºC; constant within 1ºC in the test vessels. The temperature monitored continuously in an adjacent vessel varied by more than 1ºC, but was not considered to have adversely affected the integrity of the test since no immobilization was observed.
- pH:
- 7.72 to 8.28
- Dissolved oxygen:
- 8.55 – 9.22 mg/L (93 – 97% air saturation value)
- Salinity:
- Not specified.
- Conductivity:
- Not specified.
- Nominal and measured concentrations:
- See Table 2 (below).
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 100 mL (nominal) glass, tall form beakers covered with clear lids
- Test solution volume: 50 mL (nominal)
- Aeration: not specified
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
- No. of vessels per vehicle control (replicates): not applicable
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Elendt M4 medium prepared from trace element stock solutions and reverse-osmosis (RO) water in accordance with OECD Guideline No. 202.
OTHER TEST CONDITIONS
- Intervals of water quality measurement: 0 and 48 hours
- Adjustment of pH: none
- Photoperiod: 16-hour light : 8-hour dark
- Light intensity: not specified
EFFECT PARAMETERS MEASURED (with observation intervals if applicable):
The EL50 values, no observed effect loading rate (NOEL) and the lowest observed effect loading rate (LOEL) were estimated empirically by observation of the data.
VEHICLE CONTROL: not applicable
RANGE-FINDING STUDY
- Test concentrations: 0, 1.0, 10 and 100 mg/L (duplicate vessels for each)
- Results used to determine the conditions for the definitive study: See immobilization data in Table 1 (below). - Reference substance (positive control):
- yes
- Duration:
- 24 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 100 other: mg/L loading rate WAF
- Nominal / measured:
- nominal
- Conc. based on:
- other: nominal loading rate WAF
- Basis for effect:
- mobility
- Duration:
- 24 h
- Dose descriptor:
- NOELR
- Effect conc.:
- 100 other: mg/L loading rate WAF
- Nominal / measured:
- nominal
- Conc. based on:
- other: nominal mg/L loading rate WAF
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 100 other: mg/L loading rate WAF
- Nominal / measured:
- nominal
- Conc. based on:
- other: nominal mg/L loading rate WAF
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- NOELR
- Effect conc.:
- 100 other: mg/L loading rate WAF
- Nominal / measured:
- nominal
- Conc. based on:
- other: nominal mg/L loading rate WAF
- Basis for effect:
- mobility
- Details on results:
- - Behavioral abnormalities: none
- Immobilization in negative control: none
- Other adverse effects in negative control: none
- Abnormal responses: none
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: All WAF exposure preparations were colorless solutions indicating that no undissolved test substance was present. The apparent decrease in concentration at the 100 mg/L loading rate WAF after 48 hours, however, could be attributed to the presence of microscopic particles or micelles, which were not readily visible and which may have settled out of solution over the test period, given the stability observed in the remaining WAFs. This was considered not to have affected the integrity of the test given that no immobilization was observed at any loading rate during the test. Given that the test substance is a multi-constituent substance, the results were based on nominal loading rates.
- Effect concentrations exceeding solubility of substance in test medium: yes - Results with reference substance (positive control):
- - Reference substance: potassium dichromate
- Test design: same test organism, medium, exposure conditions and replication as this definitive test
- Results with reference substance valid? Yes; EC50 result was within the expected range state in the OECD Guideline No. 202 (0.6 - 2.1 mg/L).
- Relevant effect levels: 48-hour EC50
- Dose-response test: yes; treatment concentrations were 0 (control), 0.32, 0.56, 1.0, 1.8 and 3.2 mg/L
- EC50: 1.366 mg/L
- NOEC: 1.0 mg/L - Reported statistics and error estimates:
- Statistical analysis was not performed given that no immobilisation was observed during the test.
- Validity criteria fulfilled:
- yes
- Remarks:
- The validity criteria for control immobility (≤10%) and dissolved oxygen (≥3 mg/L) were both satisfied. The test is therefore considered valid.
- Conclusions:
- No immobilization was observed after 48 hours of exposure. The 48-hour EL50 value was therefore considered to be >100 mg/L loading rate WAF. The test showed no toxicity at the limit of solubility of the test substance in the test media.
- Executive summary:
The study was conducted in accordance with the requirements of OECD Chemicals Testing Guideline No. 202. Test solutions were prepared as Water Accommodated Fractions (WAFs) based on the recommendations of OECD Series on Testing and Assessment, No. 23. Based on the results of a range-finding test the definitive test was conducted at nominal loading rates of 1.0, 3.2, 10, 32 and 100 mg/L under static conditions, with a concurrent control group.
At the start of the test, five juvenile Daphnia magna were added to each test vessel. The Daphnia magna in each test vessel were observed for mobility at 24 and 48 hours. The Daphnia magna were not fed during the test.
Samples of test media were analyzed at0 (fresh media) and 48 hours (old media) usinghigh performance liquid chromatography (HPLC) with time of flight mass spectrometry (TOF) based on quantitation of the dithiophosphatefraction (without molybdenum) of the test substance. Analysis of the test media confirmed measured concentrations to range from 0.0262 to 0.769 mg/L at 0 hours and from 0.0299 to 0.237 mg/L at 48 hours. Given that the test substance is a multi-constituent substance and analytical monitoring was limited to the dithiophosphatefraction (without molybdenum) of the test substance, the effect concentrations were based on nominal loading rates.
No immobilization was observed over the 48-hour exposure period. The 48-hour EL50 value was therefore determined to be >100 mg/L loading rate WAF and the No Observed Effect Loading rate (NOEL) was determined to be 100 mg/L loading rate WAF. The test showed no toxicity at the limit of solubility of the test substance in the test media.
The validity criteria for control immobility (≤10%) and dissolved oxygen (≥3 mg/L) were both satisfied. The test is therefore considered valid.
Reference
Table 1: Immobilization in rangefinding test
Nominal |
Cumulative immobilised Daphnia magna (initial population: 5 Daphnia per replicate) |
||||
loading rate |
24 hours |
48 hours |
% |
||
(mg/L) |
R1 |
R2 |
R1 |
R2 |
|
Control |
0 |
0 |
0 |
0 |
0 |
1.0 |
0 |
0 |
0 |
1 |
10 |
10 |
0 |
0 |
1 |
0 |
10 |
100 |
0 |
0 |
0 |
0 |
0 |
R = Replicate
Table 2: Analysis of test media during the definitive test
Nominal |
Measured Concentration* (mg/L) |
|
loading rate |
0 Hours |
48 Hours |
(mg/L) |
(New) |
(Old) |
Control |
<LOQ |
<LOQ |
1.0 |
0.0262 |
0.0299 |
3.2 |
0.0277 |
0.0161 |
10 |
0.135 |
0.126 |
32 |
0.229 |
0.200 |
100 |
0.769 |
0.237 |
* Based on quantitation of dithiophosphate fraction (without molybdenum)
LOQ = Limit of quantification (0.01 mg/L)
Table 3: Immobilization in definitive test
Nominal loading rate (mg/L) |
Number of |
% Immobility |
% Immobility |
Control |
20 |
0 |
0 |
1.0 |
20 |
0 |
0 |
3.2 |
20 |
0 |
0 |
10 |
20 |
0 |
0 |
32 |
20 |
0 |
0 |
100 |
20 |
0 |
0 |
Description of key information
In an OECD 202 study, conducted according to GLP, the acute toxicity of the test item to the freshwater invertebrate Daphnia magna was investigated under static conditions and the 48 -Hour EC50 value was determined to be greater than 100 mg/L loading rate WAF and the No Observed Effect Loading rate (NOEL) was determined to be 100 mg/L loading rate WAF (Smithers Viscient (ESG) Ltd, ****).
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 100 mg/L
Additional information
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.
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