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EC number: 946-797-7 | 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:
- 2007-08-03 to 2007-09-13
- 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)
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Sampling method: Water samples were taken from each test chamber prior to test initiation (pre-test), at test initiation and at test termination. Water samples (10 mL) were collected using a 10 mL volumetric pipette and placed in a 20-mL glass scintillation vial.
- Vehicle:
- yes
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: The nominal test concentrations were selected on the basis of the reported solubility of the substance (34 μg/L). A primary stock was prepared by isotropic dilution of the 14C-labeled L3 with non-radiolabeled L3. A 7.0 μL aliquot of 14C-L3 (0.00583 g) was added to a 1.0 mL vial. A 200 μL aliquot (0.16344 g) of L3 was also added to the vial. Approximately 0.5 mL of dimethyl formamide (DMF) was added to the vial and the contents of the vial was transferred to a 500-mL volumetric flask. The flask was then brought to volume with DMF, and mixed well. Three 0.1 mL aliquots of the primary stock were counted by LSC. The specific activity of the primary stock was determined to be 6.743 μCi/mg.
Four additional stock solutions were prepared at concentrations of 170, 85, 43 and 21 mg/L by proportional dilution of the primary stock with DMF. DMF only was used as the solvent control. The stock solutions were delivered to the diluter mixing chambers (at a rate of 0.0125 mL/minute) where they were diluted with dilution water (at a rate of 125 mL/min) to achieve the desired test concentrations. The concentration of DMF in the solvent control and the treated media was 0.1 mL/L. Test vessels and mixing chambers remained clear and colourless throughout the test. - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Source, supplier, any pretreatment, breeding method: Dow Corning in-house Cultures. The cultures were initiated with organisms obtained from Aquatic Biosystems Inc., Fort Collins, Colorado.
- Age at study initiation: <24 hours old
_ Culture conditions: Daphnia were cultured in dilution water at 20+/-2° under cool white fluorescent lighting with a 16:8 h light:dark photoperiod and a light intensity of 100+/-50 foot candles. They were fed on a diet of Selenastrum capricornutum and YCT (yeast, cerophyl and trout chow). Daphnids were not fed during the test. - Test type:
- flow-through
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- Hardness 132 mg/L as CaCO3, Alkalinity 45 mg/L as CaCO3
- Test temperature:
- 19.7 to 20.2ºC
- pH:
- 7.3-7.6
- Dissolved oxygen:
- ≥8.0 mg/L (90% ASV)
- Salinity:
- Not applicable
- Nominal and measured concentrations:
- Nominal concentrations: Negative Control, Solvent Control, 2.1, 4.3, 8.5, 17 and 34 μg/L
Mean measured concentrations:
The mean measured concentrations in the treated media corresponded to 57, 49, 55, 56 and 59% of the nominal values respectively.
The results are reported with reference to mean measured concentrations. - Details on test conditions:
- TEST SYSTEM
- Exposure vessel type: The test compartments were 300-mL glass beakers with 2 holes on opposite sides covered with nylon screen. The test chambers were placed in 7.5-L polyethylene aquaria containing 3.4 L of test solution.
- Flow-through rate: Each replicate received approximately 26 volume additions per day delivered by rotameters. The rate of addition was set relatively high to compensate for the relatively high volatility of the test substance (vapour pressure 4 mm at 25°C).
- Dilution water source: Dechlorinated Municipal Water
- Dilution water chemistry (hardness, alkalinity, pH, TOC, TSS, salinity, Ca/Mg ration, Na/K ratio): Hardness 132 mg/L as CaCO3, Alkalinity 45 mg/L as CaCO3, pH 7.3-7.6, Conductivity 384 mhos/cm and Total Residual Chlorine <10 g/L
- Lighting (quality, intensity, and periodicity): Wavelength similar to natural sunlight, 55 to 62 foot-candles, 16 hours light:8 hours dark
- Water chemistry in test: DO, pH and temperature measured in each test chamber daily
- Element (unit) basis (i.e., immobilization): Mortality and immobilization
- Test design (number of replicates, individuals per replicate, concentrations): Two replicates/treatment, 10 individuals/replicate
- Method of calculating mean measured concentrations: Arithmetic mean. - Reference substance (positive control):
- no
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 20 µg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- - Immobilisation of control: 0
- Reported statistics and error estimates:
- No significant effects on mobility or mortality were recorded in the highest treatment. An EC50 value could therefore not be determined.
- Validity criteria fulfilled:
- yes
- Conclusions:
- A 48-hour EC50 value of >20 μg/L has been determined for the effects of the substance on mobility of Daphnia magna based on geometric mean measured concentrations. The results were obtained under flow-through test conditions.
Reference
Table 1. Test results
Nominal concentration (μg/L) | Mean measured concentration (μg/L) | Mean percentage immobilisation after 24 hours | Mean percentage immobilisation after 48 hours |
0 (Control) | <LoQ | 0 | 0 |
0 (Vehicle control) | <LoQ | 0 | 0 |
2.1 | 1.2 | 0 | 0 |
4.3 | 2.1 | 0 | 0 |
8.5 | 4.7 | 0 | 0 |
17 | 9.5 | 0 | 0 |
34 | 20 | 0 | 5 |
The geometric mean of the highest concentration tested has been calculated to be 20 μg/L by the current reviewer.
Description of key information
HMDS: There are no reliable data for short-term toxicity to aquatic invertebrates. However, the requirement to test is waived in accordance with Column 2 specific rules for adaptation from Column 1 of REACH Annex VII.
L3: Short-term toxicity to invertebrates: 48 h EC50 >20 μg/l (measured, geom. mean; highest concentration tested) (OECD 202).
L4: There are no reliable data for short-term toxicity to aquatic invertebrates. However, the requirement to test is waived in accordance with Column 2 specific rules for adaptation from Column 1 of REACH Annex VII.
L5: There are no reliable data for short-term toxicity to aquatic invertebrates. However, the requirement to test is waived in accordance with Column 2 specific rules for adaptation from Column 1 of REACH Annex VII.
Key value for chemical safety assessment
Additional information
Constituent HMDS
There are no reliable data for short-term toxicity to aquatic invertebrates. However, the requirement to test is waived in accordance with Column 2 specific rules for adaptation from Column 1 of REACH Annex VII.
Constituent L3:
A 48-hour EC50 value of >20 μg/l (highest concentration tested) has been determined for the effects of the substance on mobility of Daphnia magna based on geometric mean measured concentrations. In view of the use of flow-through test conditions it is likely that the test organisms were exposed primarily to the parent substance (DCC, 2007).
Constituent L4
There are no reliable data for short-term toxicity to aquatic invertebrates. However, the requirement to test is waived in accordance with Column 2 specific rules for adaptation from Column 1 of REACH Annex VII.
Constituent L5
There are no reliable data for short-term toxicity to aquatic invertebrates. However, the requirement to test is waived in accordance with Column 2 specific rules for adaptation from Column 1 of REACH Annex VII.
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