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EC number: 937-739-1 | CAS number: 1128123-94-3
- 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
Hydrolysis
Administrative data
Link to relevant study record(s)
- Endpoint:
- hydrolysis
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Testing was conducted between 15 June 2011 and 20 December 2011.
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Remarks:
- Study conducted in compliance with agreed protocols, with no or minor deviations from standard test guidelines and/or minor methodological deficiencies, which do not affect the quality of the relevant results. The study report was conclusive, done to a valid guideline and the study was conducted under GLP conditions.
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 111 (Hydrolysis as a Function of pH)
- Deviations:
- no
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method C.7 (Degradation: Abiotic Degradation: Hydrolysis as a Function of pH)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Radiolabelling:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- The buffer solutions were filtered through a 0.2 µm membrane filter to ensure they were sterile before commencement of the test. Also these solutions were subjected to ultrasonication and degassing with nitrogen to minimise dissolved oxygen content.
Preparation of samples:
Sample solutions were prepared in stoppered glass flasks at a nominal concentration of 6 g/l in the three buffer solutions.
The test solutions were split into individual vessels for each data point.
The solutions were shielded from light whilst maintained at the test temperature.
Preliminary test/Tier 1:
Sample solutions at pH 4, 7 and 9 were maintained at 50.0 ± 0.5°C for a period of 144 hours.
Analysis of sample solutions:
The sample solutions were taken from the water bath at various times and the pH of each solution recorded.
The concentration of the sample solution was determined by high performance liquid chromatography (HPLC).
Samples:
Duplicate aliquots (A and B) of sample solution were diluted by a factor of 10 using reverse osmosis water.
Standards:
Standard solutions of test item were prepared in relevant buffer solution:reverse osmosis water (1:9 v/v) covering a nominal concentration range of 60 to 900 mg/l including a duplicate at a nominal concentration of approximately 600 mg/l.
Matrix blanks
Relevant buffer solution:reverse osmosis water (1:9 v/v). - Buffers:
- Specification of buffer solutions:
Buffer solution (pH 4):
Components: Potassium hydrogen phthalate
Concentration (mol dm-3): 0.05
Buffer solution (pH 7):
Components: Disodium hydrogen orthophosphate (anhydrous), Potassium dihydrogen orthophosphate, Sodium chloride
Concentration (mol dm-3): 0.03, 0.02, 0.02
Buffer solution (pH 9):
Components: Dosodium tetraborate, Sodium chloride
Concentration (mol dm-3): 0.01, 0.02
The buffer solutions were filtered through a 0.2 µm membrane filter to ensure they were sterile before commencement of the test. Also these solutions were subjected to ultrasonication and degassing with nitrogen to minimise dissolved oxygen content. - Estimation method (if used):
- Not used.
- Details on test conditions:
- Refer to details on sampling and analytical methods.
- Duration:
- 144 h
- pH:
- 4
- Initial conc. measured:
- 6 other: g/l: theoretical concentration
- Duration:
- 144 h
- pH:
- 7
- Initial conc. measured:
- 6 other: g/l: theoretical concentration
- Duration:
- 144 h
- pH:
- 9
- Initial conc. measured:
- 6 other: g/l: theoretical concentration
- Number of replicates:
- Duplicate aliquots (A and B) of sample solution were diluted by a factor of 10 using reverse osmosis water.
- Positive controls:
- no
- Negative controls:
- no
- Statistical methods:
- Not specified.
- Preliminary study:
- The mean peak areas relating to the standard and sample solutions are shown in any other information on results including tables and figures section.
The calibration curves from which the sample concentrations were interpolated are shown in Figure 11.1 to Figure 11.12 (see attached background material - calibration curves). - Transformation products:
- no
- Details on hydrolysis and appearance of transformation product(s):
- At pH4, 7 and 9 there was less than 10% hydrolysis over 120 hours at 50°C, equivalent to a half-life greater than 1 year at 25°C.
- Key result
- pH:
- 4
- Temp.:
- 25 °C
- DT50:
- > 1 yr
- Key result
- pH:
- 7
- Temp.:
- 25 °C
- DT50:
- > 1 yr
- Key result
- pH:
- 9
- Temp.:
- 25 °C
- DT50:
- > 1 yr
- Other kinetic parameters:
- None.
- Details on results:
- At pH 4, 7 and 9 there was less than 10% hydrolysis over 120 hours at 50°C, equivalent to a half-life greater than 1 year at 25°C.
- Validity criteria fulfilled:
- not applicable
- Conclusions:
- The estimated half-life at 25°C of the test material at pH 4, 7 and 9 is greater than 1 year.
- Executive summary:
Thehydrolysis determination was carried out using a procedure designed to be compatible with Method C7 Abiotic Degradation, Hydrolysis as a Function of pH of Commission Regulation (EC) No 440/2008 of 30 May 2008 and Method 111 of the OECD Guidelines for Testing of Chemicals, 13 April 2004.
The estimated half-lives at 25°C of the test item are shown in the following table:
pH
Estimated half-life at 25°C
4
>1 year
7
>1 year
9
>1 year
Reference
Preliminary test/Tier 1
The mean peak areas relating to the standard and sample solutions are shown in the following table:
Solution |
Mean Peak Area |
Standard 924 mg/l |
2.289 x 108 |
Standard 822 mg/l |
2.104 x 108 |
Standard 616 mg/l |
1.457 x 108 |
Standard 620 mg/l |
1.607 x 108 |
Standard 308 mg/l |
7.038 x 107 |
Standard 103 mg/l |
1.591 x 107 |
Standard 61.6 mg/l |
5.680 x 106 |
Matrix Blank |
0.000 |
Initial Sample A, pH 4 |
1.239 x 108 |
Initial Sample B, pH 4 |
1.117 x 108 |
Standard 909 mg/l |
3.244 x 108 |
Standard 808 mg/l |
2.595 x 108 |
Standard 606 mg/l |
1.518 x 108 |
Standard 697 mg/l |
2.431 x 108* |
Standard 303 mg/l |
2.982 x 108 |
Standard 101 mg/l |
6.163 x 107 |
Standard 60.6 mg/l |
1.398 x 106 |
continued
Solution |
Mean Peak Area |
Matrix Blank |
0.000 |
Initial Sample A, pH 7 |
1.892 x 108 |
Initial Sample B, pH 7 |
1.999 x 108 |
Standard 931 mg/l |
4.030 x 108 |
Standard 827 mg/l |
3.268 x 108 |
Standard 620 mg/l |
2.034 x 108 |
Standard 671 mg/l |
2.352 x 108 |
Standard 310 mg/l |
6.579 x 107 |
Standard 103 mg/l |
1.118 x 107 |
Standard 62.0 mg/l |
4.300 x 106 |
Matrix Blank |
0.000 |
Initial Sample A, pH 9 |
1.775 x 108 |
Initial Sample B, pH 9 |
1.860 x 108 |
Standard 924 mg/l |
2.978 x 108 |
Standard 822 mg/l |
2.164 x 108 |
Standard 643 mg/l |
1.734 x 108 |
Standard 604 mg/l |
1.530 x 108 |
Standard 308 mg/l |
4.684 x 107 |
Standard 103 mg/l |
5.441 x 106 |
Standard 61.6 mg/l |
2.222 x 106 |
Matrix Blank |
0.000 |
24-Hour Sample A, pH 4 |
1.506 x 108 |
24-Hour Sample B, pH 4 |
1.606 x 108 |
Standard 909 mg/l |
2.850 x 108 |
Standard 808 mg/l |
2.287 x 108 |
Standard 606 mg/l |
1.560 x 108 |
Standard 697 mg/l |
1.809 x 108 |
Standard 303 mg/l |
6.120 x 107 |
Standard 101 mg/l |
1.135 x 107 |
Standard 60.6 mg/l |
3.310 x 106 |
Matrix Blank |
0.000 |
24-Hour Sample A, pH 7 |
1.190 x 108 |
24-Hour Sample B, pH 7 |
1.376 x 108 |
*This point was an outlier and therefore has not been used in the calculations.
Solution |
Mean Peak Area |
Standard 931 mg/l |
3.148 x 108 |
Standard 827 mg/l |
2.059 x 108 |
Standard 609 mg/l |
1.431 x 108 |
Standard 633 mg/l |
1.613 x 108 |
Standard 310 mg/l |
5.071 x 107 |
Standard 103 mg/l |
1.013 x 107 |
Standard 62.0 mg/l |
4.043 x 106 |
Matrix Blank |
0.000 |
24-Hour Sample A, pH 9 |
1.569 x 108 |
24-Hour Sample B, pH 9 |
1.435 x 108 |
Standard 924 mg/l |
3.156 x 108 |
Standard 822 mg/l |
2.591 x 108 |
Standard 616 mg/l |
1.774 x 108 |
Standard 640 mg/l |
1.919 x 108 |
Standard 308 mg/l |
5.006 x 107 |
Standard 103 mg/l |
6.765 x 106 |
Standard 61.6 mg/l |
1.561 x 106 |
Matrix Blank |
0.000 |
120-Hour Sample A, pH 4 |
1.798 x 108 |
120-Hour Sample B, pH 4 |
1.852 x 108 |
Standard 909 mg/l |
3.888 x 108 |
Standard 808 mg/l |
3.242 x 108 |
Standard 606 mg/l |
1.963 x 108 |
Standard 604 mg/l |
2.014 x 108 |
Standard 308 mg/l |
5.864 x 107 |
Standard 103 mg/l |
1.123 x 107 |
Matrix Blank |
0.000 |
120-Hour Sample A, pH 7 |
2.050 x 108 |
120-Hour Sample B, pH 7 |
1.929 x 108 |
continued
Solution |
Mean Peak Area |
Standard 931 mg/l |
3.522 x 108 |
Standard 827 mg/l |
2.846 x 108 |
Standard 609 mg/l |
1.993 x 108 |
Standard 633 mg/l |
2.025 x 108 |
Standard 310 mg/l |
6.444 x 107 |
Standard 103 mg/l |
1.201 x 107 |
Standard 62.0 mg/l |
5.471 x 106 |
Matrix Blank |
0.000 |
120-Hour Sample A, pH 9 |
1.829 x 108 |
120-Hour Sample B, pH 9 |
1.704 x 108 |
Standard 924 mg/l |
3.427 x 108 |
Standard 822 mg/l |
2.990 x 108 |
Standard 616 mg/l |
1.956 x 108 |
Standard 640 mg/l |
2.084 x 108 |
Standard 308 mg/l |
5.992 x 107 |
Standard 103 mg/l |
6.774 x 106 |
Standard 61.6 mg/l |
2.303 x 106 |
Matrix Blank |
0.000 |
144-Hour Sample A, pH 4 |
2.072 x 108 |
144-Hour Sample B, pH 4 |
2.069 x 108 |
Standard 909 mg/l |
5.135 x 108 |
Standard 808 mg/l |
4.329 x 108 |
Standard 606 mg/l |
2.947 x 108 |
Standard 604 mg/l |
2.681 x 108 |
Standard 308 mg/l |
1.037 x 108 |
Standard 103 mg/l |
2.988 x 107 |
Standard 60.6 mg/l |
1.719 x 107 |
Matrix Blank |
0.000 |
144-Hour Sample A, pH 7 |
2.365 x 108 |
144-Hour Sample B, pH 7 |
2.506 x 108 |
Solution |
Mean Peak Area |
Standard 931 mg/l |
4.002 x 108 |
Standard 827 mg/l |
3.175 x 108 |
Standard 620 mg/l |
1.715 x 108 |
Standard 655 mg/l |
1.728 x 108 |
Standard 310 mg/l |
6.619 x 107 |
Standard 103 mg/l |
1.664 x 107 |
Standard 62.0 mg/l |
3.959 x 106 |
Matrix Blank |
0.000 |
144-Hour Sample A, pH 9 |
1.500 x 108 |
144-Hour Sample B, pH 9 |
1.487 x 108 |
The test item concentrations at the given time points are shown in the following tables
pH 4 at 50.0 ± 0.5ºC
|
Time (Hours) |
|||||||
Initial (A) |
Initial (B) |
24 (A) |
24 (B) |
120 (A) |
120 (B) |
144 (A) |
144 (B) |
|
Concentration (g/l) |
5.15 |
4.68 |
6.19 |
6.44 |
6.40 |
6.52 |
6.48 |
6.48 |
% of theoretical concentration (6.03 g/l) |
85.4 |
77.5 |
103 |
107 |
106 |
108 |
107 |
107 |
Result: Less than 10% hydrolysis over 120 hours at 50°C, equivalent to a half-life greater than 1 year at 25°C*
pH 7 at 50.0 ± 0.5ºC
|
Time (Hours) |
|||||||
Initial (A) |
Initial (B) |
24 (A) |
24 (B) |
120 (A) |
120 (B) |
144 (A) |
144 (B) |
|
Concentration (g/l) |
6.88 |
7.09 |
5.15 |
5.70 |
6.24 |
6.01 |
5.50 |
5.73 |
% of theoretical concentration (6.14 g/l) |
112 |
116 |
83.8 |
92.9 |
102 |
97.9 |
89.6 |
93.3 |
Result: Less than 10% hydrolysis over 120 hours at 50°C, equivalent to a half-life greater than 1 year at 25°C*
pH 9 at 50.0 ± 0.5ºC
|
Time (Hours) |
|||||||
Initial (A) |
Initial (B) |
24 (A) |
24 (B) |
120 (A) |
120 (B) |
144 (A) |
144 (B) |
|
Concentration (g/l) |
5.74 |
5.90 |
6.48 |
6.13 |
6.01 |
5.72 |
5.70 |
5.68 |
% of theoretical concentration (6.05 g/l) |
94.9 |
97.6 |
107 |
101 |
99.3 |
94.6 |
94.2 |
93.8 |
Result: Less than 10% hydrolysis over 120 hours at 50°C, equivalent to a half-life greater than 1 year at 25°C
*
Results from the analysis of the pH 4 and pH 7 initial time points were considered inconsistent with the subsequent data, therefore the percentage of theoretical concentration has been presented, see Overall remarks, Discussion.
Description of key information
The estimated half-lives at 25°C of the test item, at pH 4, 7 and 9 is greater than 1 year.
Key value for chemical safety assessment
- Half-life for hydrolysis:
- 1 yr
- at the temperature of:
- 25 °C
Additional information
The determination was carried out using a procedure designed to be compatible with Method C7 Abiotic Degradation, Hydrolysis as a Function of pH of Commission Regulation (EC) No 440/2008 of 30 May 2008 and Method 111 of the GECD Guidelines for Testing of Chemicals, 13 April 2004.
Less than 10% hydrolysis of the test item occurred over a 120 -hour period, equivalent to a half-life greater than 1 year at 25°C.
The estimated half-lives at 25°C of the test item are:
pH |
Estimated half-life at 25°C |
4 |
>1 year |
7 |
>1 year |
9 |
>1 year |
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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