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EC number: - | 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
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- Repeated dose toxicity
- Genetic toxicity
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- Specific investigations
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- 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:
- 2016-03-23 to 2016-05-12
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline 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
- GLP compliance:
- no
- Type of method:
- column elution method
- Key result
- Water solubility:
- 0.14 mg/L
- Conc. based on:
- test mat.
- Incubation duration:
- 71 h
- Temp.:
- 20 °C
- pH:
- >= 6.9 - <= 7
- Conclusions:
- The water solubility of the test item at a temperature of 20 °C was determined to be 0.140 mg/L.
- Executive summary:
The water solubility of the test item was determined according to OECD 105 and Regulation (EC) No. 440/2008 method A.6 using the column elution method with HPLC analysis. About 102.2 mg of the test item were dissolved in 100 mL acetone. For charging the columns in each case 25 mL of the test item solution was added to about 3 g of sea sand and the mixtures were shaken. The solvent was then removed under reduced pressure using a rotary evaporator (40 °C, approx. 20 mbar). The dry residues were placed into the columns of the test apparatus, which have afterwards been filled with water (test temperature: 20 °C; water pH at 23 °C: 6.1). After a swelling time of 2 h, pumps were started to rinse the test item coated sand with demineralized water. At the end of the study it was confirmed that residual test item remained on the columns. The concentration of test item was determined by means of HPLC. The pH of each sample was recorded. The water solubility of the test item was determined to be 0.140 mg/L at 20 °C (pH = 6.9 – 7.0).
Reference
Preliminary visual estimation of the water solubility
Three preliminary tests were carried out with specified amounts of the test item and 100 mL and 500 mL demineralized water, respectively. After each addition of an amount of water, the mixture was stirred for at least 24 hours, and visually checked for any undissolved particles.
Results of the preliminary visual estimation of the water solubility
Amount |
Total volume of |
Appearance of mixture |
8.8 |
100 |
not dissolved |
11.6 |
500 |
not dissolved |
4.4 |
500 |
not dissolved |
The preliminary visual experiments showed that the water solubility of the test item is < 10 mg/L. According to the preliminary visual estimation in the main test the water solubility was determined by the column elution method.
Column elution method
102.2 mg of the test item were dissolved in 100 mL acetone. For charging the columns in each case 25 mL of the test item solution was added to about 3 g of sea sand and the mixtures were shaken. The solvent was then removed under reduced pressure using a rotary evaporator (40 °C, approx. 20 mbar). The dry residues were placed into the columns of the test apparatus, which have afterwards been filled with water (test temperature: 20 °C; water pH at 23 °C: 6.1). After a swelling time of 2 h pumps were started to rinse the test item coated sand with demineralized water. At the end of the study it was confirmed that residual test item remained on the columns. The residual test item was eluted with 50 mL acetone. As blank value the used demineralized water was tested. No signal was detected in the range of the retention time of the test item. The concentration of the test item was quantified by HPLC.
Column elution method, column 12.5 mL/h (fraction 21 to 25)
Fraction no. |
V /mL |
pH |
water solubility |
21 |
19.0 |
6.9 |
0.131 |
22 |
19.0 |
6.9 |
0.132 |
23 |
18.7 |
6.9 |
0.133 |
24 |
18.7 |
6.9 |
0.133 |
25 |
18.7 |
6.9 |
0.137 |
Due to the slight tendency of the results five additional fractions have been analysed.
Column elution method, column 12.5 mL/h (fractions 37 to 41)
Fraction no. |
V /mL |
PH |
water solubility |
37 |
18.7 |
6.7 |
0.130 |
38 |
18.7 |
6.9 |
0.133 |
39 |
18.7 |
6.8 |
0.134 |
40 |
18.7 |
6.9 |
0.135 |
41 |
18.7 |
6.9 |
0.137 |
As the water solubility was in the same range for each of the five fraction series (both starting at 0.13 mg/L and going to 0.14 mg/L) the observed tendency was evaluated as not significant. The water solubility was found to be 0.133 mg/L.
Column 25.0 mL/h:
Rotation period of the fraction collector: 45 min per fraction Duration of sampling: about 47 h (63 fractions)
Column elution method, column 25.0 mL/h
Fraction no. |
V /mL |
pH |
water solubility |
48 |
19.8 |
6.9 |
0.145 |
49 |
19.8 |
7.0 |
0.138 |
50 |
19.8 |
6.9 |
0.137 |
51 |
20.0 |
6.9 |
0.140 |
52 |
20.0 |
7.0 |
0.141 |
The water solubility was found to be 0.140 mg/L.
In both columns the concentration of five consecutive fractions was constant within ± 30 %. No increasing or decreasing tendency was observed.
Description of key information
The water solubility of the test item at a temperature of 20 °C was determined to be 0.140 mg/L.
Key value for chemical safety assessment
- Water solubility:
- 0.14 mg/L
- at the temperature of:
- 20 °C
Additional information
The water solubility of the test item was determined according to OECD 105 and Regulation (EC) No. 440/2008 method A.6 using the column elution method with HPLC analysis. About 102.2 mg of the test item were dissolved in 100 mL acetone. For charging the columns in each case 25 mL of the test item solution was added to about 3 g of sea sand and the mixtures were shaken. The solvent was then removed under reduced pressure using a rotary evaporator (40 °C, approx. 20 mbar). The dry residues were placed into the columns of the test apparatus, which have afterwards been filled with water (test temperature: 20 °C; water pH at 23 °C: 6.1). After a swelling time of 2 h, pumps were started to rinse the test item coated sand with demineralized water. At the end of the study it was confirmed that residual test item remained on the columns. The concentration of test item was determined by means of HPLC. The pH of each sample was recorded. The water solubility of the test item was determined to be 0.140 mg/L at 20 °C (pH = 6.9 – 7.0).
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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