Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 938-422-0 | 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:
- 2012-07-18 to 2012-08-24
- 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:
- 0.028 mg/L
- Conc. based on:
- test mat.
- Incubation duration:
- 71 h
- Temp.:
- 20 °C
- pH:
- 6
- Details on results:
- The water solubility of the test item at a temperature of 20 °C was determined to 0.028 mg/L.
- Conclusions:
- The water solubility of the test item at a temperature of 20 °C was determined to 0.028 mg/L.
- Executive summary:
The water solubility was determined according to OECD 105 using the column elution method with HPLC analysis (reference 4.8 -1). Therefore, two identical columns were prepared; one of them was exposed to a flow rate of about 12.5 mL/h (column 1), the other one to 25.0 mL/h (column 2). Another experiment was performed according to this procedure (flow rate 25.0 mL/h) but without test item ("blank" = column 3). The concentration of test item was determined by means of HPLC. Therefore the aqueous fractions were diluted from 0.75 mL to 1 mL with acetonitrile. The volumes of all fractions were measured. For the analysed fractions the pH values and the temperatures were measured, too. For column 1 the fractions 37 to 41 were evaluated. The water solubility was found to be 0.023 mg/L For column 2 the fractions 79 to 83 were evaluated. The water solubility was found to be 0.033 mg/L. The recovery of the recheck samples was between 96.6% and 104.0% indicating a sufficient accuracy of the analytical method. The water solubility at a temperature of 20 °C was determined to be 0.028 mg/L.
Reference
Preliminary Visual Estimation of the Water Solubility
Different amounts of the test item and water were stirred at room temperature until the mixtures appeared dissolved or the water solubility could be estimated to be below 10 mg/L.
Appearance of the test mixtures
Amount of the test item in mg |
Total volume in mL |
Appearance of mixture |
9.9 |
100 |
undissolved |
8.7 |
500 |
undissolved |
4.6 |
500 |
undissolved |
Concentration and pH
According to the guideline, the data of the fractions 1 to 5 were not taken into account for the following evaluation. The values for the water solubility were calculated from fractions 37 to 41 for column 1, from the fractions 79 to 83 for column 2 and from the fractions 40 to 44 for column 3.
Column 1
Fraction |
V |
PH |
water solubility |
37 |
18.1 |
5.9 |
22.66 |
38 |
18.1 |
5.9 |
23.43 |
39 |
18.1 |
5.7 |
24.52 |
40 |
18.1 |
5.4 |
23.90 |
41 |
18.1 |
5.6 |
22.17 |
According to the guideline the run can be stopped if the concentrations of five fractions do not differ more than ± 30 % without any increasing or descending tendency.
Result column 1:
Evaluation of the fractions 37 to 41
The water solubility was found to be 0.023 mg/L (without correction of the purity)
Column 2
Fraction |
V |
PH |
water solubility |
79 |
17.6 |
5.9 |
32.91 |
80 |
17.6 |
5.8 |
32.86 |
81 |
17.6 |
6.0 |
33.28 |
82 |
17.6 |
6.0 |
33.27 |
83 |
17.6 |
5.7 |
33.49 |
According to the guideline the run can be stopped if the concentrations of five fractions do not differ more than±30 % without any increasing or descending tendency.
Result column 2:
Evaluation of the fractions 79 to 83
The water solubility was found to be 0.033 mg/L (without correction of the purity)
Concentrations of standards for recheck
The recovery of the recheck samples was between 96.6 % and 104.0 % indicating a sufficient accuracy of the analytical method.
The water solubility of the test item at a temperature of 20 °C was determined to 0.028 mg/L.
Description of key information
The water solubility of the test item at a temperature of 20 °C was determined to 0.028 mg/L.
Key value for chemical safety assessment
- Water solubility:
- 0.028 mg/L
- at the temperature of:
- 20 °C
Additional information
The water solubility was determined according to OECD 105 using the column elution method with HPLC analysis (reference 4.8 -1). Therefore, two identical columns were prepared; one of them was exposed to a flow rate of about 12.5 mL/h (column 1), the other one to 25.0 mL/h (column 2). Another experiment was performed according to this procedure (flow rate 25.0 mL/h) but without test item ("blank" = column 3). The concentration of test item was determined by means of HPLC. Therefore the aqueous fractions were diluted from 0.75 mL to 1 mL with acetonitrile. The volumes of all fractions were measured. For the analysed fractions the pH values and the temperatures were measured, too. For column 1 the fractions 37 to 41 were evaluated. The water solubility was found to be 0.023 mg/L For column 2 the fractions 79 to 83 were evaluated. The water solubility was found to be 0.033 mg/L. The recovery of the recheck samples was between 96.6% and 104.0% indicating a sufficient accuracy of the analytical method. The water solubility at a temperature of 20 °C was determined to be 0.028 mg/L.
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.