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EC number: 947-581-5 | CAS number: 2209852-19-5
- 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
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- 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

Water solubility
Administrative data
Link to relevant study record(s)
- Endpoint:
- water solubility
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 19-03-2018 to 24-03-2018
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study performed under GLP. All relevant validity criteria were met.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 105 (Water Solubility)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.6 (Water Solubility)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- inspected: June 2016; signature: January 2017
- Type of method:
- flask method
- Water solubility:
- 429 mg/L
- Conc. based on:
- test mat.
- Temp.:
- 20 °C
- pH:
- 4.4
- Remarks on result:
- other: Mean of 24, 48 and 72 h: deviation between replicates was: 8.4%
- Conclusions:
- Interpretation of results: moderately soluble (100-1000 mg/L)
The test item water solubility was determined to be 429 mg/L of solution at pH 4.4 and 20.0 °C - Executive summary:
The water solubility of the substance was determined according to the flask method: OECD Method 105 and EU Method A.6 in accordance with GLP. Determinations were conducted using preincubation with a stirring rate of 300 rpm at 30 ± 0.5 °C, then 24 hours equilibration with a stirring rate of 100 rpm for at 20 ± 0.5 °C prior to sampling. The analytical method (GC MS, external standard) for the determination of the test item was validated and tested with satisfactory results in regard to linearity, accuracy, precision and specificity. The mean water solubility of the substance was determined to be 429 mg/L of solution at pH 4.4 and 20.0 °C.
Reference
Preliminary test
The solubility was determined to be 444 mg/L (mean value of both aliquots).For the definitivetest, the water system was changed to purified water (18.2 MOhm/cm) from double distilled water.
Definitive test:
The solubility of the test item in double distilled water was determined employing the flask method slow stirring approach at 20 ± 0.5 °C with preincubation at 30 ± 0.5 °C. The water solubility was respectively at pH 4.4:
Table 1.0. Water Solubility Results
Preincubation time |
Replicate No. |
Test Item [mg/L] |
|
Concentration #1), # 3) |
Mean |
||
24 h |
1 |
442 |
449 |
2 |
455 |
||
48 h |
1 |
424 |
424 |
2 |
423 |
||
72 h |
1 |
412 |
414 |
2 |
415 |
||
Mean (24 - 72 h) |
|
|
429 |
Deviation [%] (24 - 72 h) #2) |
8.4% |
#1) Mean value of two injections, dilution factor of 5000 and exact weight of the standard taken into account
#2) Calculated according to formula 1
#3) The content was quantified using a calibration curve with only 4 calibration points in the range of 40 – 100 µg/L. This was deemed to be acceptable, as the linearity for the range of 10 – 100 µg/L was verified during the method validation and additionally the content of the samples was in the shortened calibration range.
Formula 1:
Deviation (%) = 100 x (maximum value - minimum value) / minimum value
Temperatures were kept constant within ± 0.5 °C. The determined solubilities for each preincubation time did not differ by more than 15 %. The analytical method (GC MS, external standard) for the determination of the test item was validated and tested with satisfactory results in regard to linearity, accuracy, precision and specificity.
Description of key information
Water Solubility: 429 mg/L at pH 4.4 and 20 °C, OECD TG 105, 2018
Key value for chemical safety assessment
- Water solubility:
- 429 mg/L
- at the temperature of:
- 20 °C
Additional information
Key study : EU Method A.6, 2018 : The water solubility of the substance was determined according to the flask method: OECD Method 105 and EU Method A.6 in accordance with GLP. Determinations were conducted using preincubation with a stirring rate of 300 rpm at 30 ± 0.5 °C, then 24 hours equilibration with a stirring rate of 100 rpm for at 20 ± 0.5 °C prior to sampling. The analytical method (GC MS, external standard) for the determination of the test item was validated and tested with satisfactory results in regard to linearity, accuracy, precision and specificity. The mean water solubility of the substance was determined to be 429 mg/L of solution at pH 4.4 and 20.0 °C.
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