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Diss Factsheets
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EC number: 437-760-1 | 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
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:
- From January 26 to February 8, 2000
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Remarks:
- The study was conducted according to an internationally recognised method, and under GLP. No deviation affected the quality of the study. The substance is considered to be adequately characterised with its purity. Therefore full validation applies.
- Reason / purpose for cross-reference:
- reference to other study
- 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
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- inspected on September 22, 1999 / signed on January 18, 2000
- Type of method:
- flask method
- Key result
- Water solubility:
- 609 mg/L
- Conc. based on:
- test mat.
- Loading of aqueous phase:
- 860 mg/L
- Incubation duration:
- 24 - 72 h
- Temp.:
- 20 °C
- pH:
- 8.6 - 9.3
- Details on results:
- The solubility of the test material in water was found to be 609 ± 8 mg/L (RSD = 1%) at 20 ± 2 °C. The resulting saturated solutions were basic (pH 8.6 to 9.3) and whitish.
- Conclusions:
- Interpretation of results (migrated information): moderately soluble (100-1000 mg/L)
- Executive summary:
The water solubility of the test substance was measured under GLP according OECD 105/EU A6 guideline, flask method.
Three measurements were performed at 48, 72 and 96 h, analysis were performed with HPLC-UV after suitable calibration, and dilution of the test samples. Equilibrium was achieved and the mean result was retained.
The water solubility of the test substance is 609 ± 8 mg/L (RSD = 1%) at 20 ± 2 °C. The resulting saturated solutions were basic (pH 8.6 to 9.3) and colourless.
Reference
Preliminary test
This test was performed at 20 °C in vessels protected from light. The pH value of the water used was 9.15.
The preliminary test indicated that the test substance was soluble in water with solubility above 10 mg/L.
On the basis of these results, the final solubility determination was undertaken using the flask method
Flask method
The test was performed at 20 ± 2 °C, in vessels protected from light.
The solubility in water was found to be 609 ± 8 mg/L with a precision of 1%.
The water used had a pH value of 9.12. In the three replicate solutions prepared, the pH values were found to be 9.25, 8.88 and 8.59 (replicates 1 to 3).
Table 4.8/1: Water solubility of test item (Flask method)
Replicate number / Sampling Time |
Water solubility (mg/L) |
|||
First dilution |
Second dilution |
Mean (n=2) |
Mean (n=6) |
|
3 / T24h |
606 |
596 |
601 |
|
2 / T48h |
608 |
616 |
612 |
|
1 / T72h |
613 |
617 |
615 |
|
|
|
|
|
609 |
|
|
|
SD |
8 |
|
|
|
RSD % |
1 |
Description of key information
Considered as moderately soluble, with equilibrium reached from 24h. pH of saturated solution: ca 9.
Key value for chemical safety assessment
- Water solubility:
- 609 mg/L
- at the temperature of:
- 20 °C
Additional information
A fully reliable experimental study, conducted according to a recognized OECD/EC method and under GLP, is available. Therefore, it is considered as a key study, and the result is retained as key value.
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.