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EC number: 232-254-5 | CAS number: 7798-23-4
- 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:
- 26 November - 16 December 2009
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.6 (Water Solubility)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- Date of Inspection: 15 September 2009 Date of Signature on Certificate: 26 November 2009
- Type of method:
- flask method
- Key result
- Water solubility:
- 1.25 g/L
- Temp.:
- 20 °C
- pH:
- ca. 4
- Conclusions:
- Interpretation of results (migrated information): soluble (1000-10000 mg/L)
The water solubility of the test material has been determined to be 1.25 g/l of solution at 20.0 ± 0.5°C.
The effect of temperature over the range 10 to 30°C has been considered not to have had a significant influence on the solubility of the test material.
The initial solution pH was also shown to influence solubility of the test material. When using an identical initial saturation period of 72 hours, the use of the pH 4 buffer solution somewhat increased the resulting test material concentration (when compared to unbuffered water) to 1.62 g/l at 20.0 ± 0.5°C (at a final solution pH of 4.0) whereas the use of the pH 9 buffer solution had negligible effect on the test material concentration. It had been anticipated that an acidic pH would suppress solubility. However, although the pH 4 buffer solution was initially more acidic than the unbuffered water, due to its buffering capacity, increased dissolution of the test material occurred before the resulting acidic solution began to suppress test material dissolution. Therefore, although the maximum observed solubility was 1.62 g/l (at a final solution pH of 4.0), the water solubility may increase further in cases where additional buffering capacity exists.
Reference
See attachment for example chromatography.
Preliminary test
The preliminary estimate of water solubility was 0.959 g/L.
Definitive test
The mean peak areas relating to the standard and sample solutions are shown in the following table:
Table 4.3
Solution |
Mean peak area* |
Standard 30.5 mg/l |
3.830 |
Standard 30.5 mg/l |
3.772 |
Sample 7A |
3.755 |
Sample 7B |
3.872 |
Sample 6A |
3.732 |
Sample 6B |
3.872 |
Sample 1A |
4.020 |
Sample 1B |
4.107 |
Sample 2A |
3.891 |
Sample 2B |
3.988 |
Standard 30.5 mg/l |
3.878 |
Standard 30.5 mg/l |
3.809 |
Sample 3A |
3.960 |
Sample 3B |
3.969 |
Sample 4A |
5.185 |
Sample 4B |
4.996 |
Sample 5A |
3.850 |
Sample 5B |
3.854 |
The concentration (g/L) of test material in the sample solutions is shown in the following table:
Table 4.4
Sample Number |
Time shaken at ~ 30ºC (hours) |
Time equilibrated at 20ºC (hours) |
Concentration (g/l) |
Solution pH |
1 |
72 |
24 |
1.31 |
3.6 |
2 |
72 |
24 [10°C] |
1.27 |
3.7 |
3 |
72 |
24 [30°C] |
1.26 |
3.6 |
4 |
72 |
24 |
1.62 |
4.0 |
5 |
72 |
24 |
1.23 |
3.9 |
6 |
48 |
24 |
1.23 |
3.7 |
7 |
24 |
24 |
1.21 |
3.7 |
Mean unbuffered water result (at 20.0 ± 0.5°C): 1.25 g/L.
Validation
The linearity of the detector response with respect to concentration was assessed over the nominal concentration range of 0 to 100 mg/L (as orthophosphate anion). This was satisfactory with a correlation coefficient of 1.000 being obtained. This work was performed as part of Harlan Laboratories Ltd Project Number 2920/0020.
Description of key information
Water solubility: 1.25 g/l (EU Method A.6, flask method, GLP)
Key value for chemical safety assessment
- Water solubility:
- 1.25 g/L
- at the temperature of:
- 20 °C
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.
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.