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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
- 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:
- May 2020 - January 2021
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 111 (Hydrolysis as a Function of pH)
- Deviations:
- no
- Principles of method if other than guideline:
- Since the test item was expected to hydrolyze rather fast, the conditions of the preliminary test were modified from the conditions given in the guideline. The test was carried out at 20 °C ± 0.5 °C. Samples were taken at the start and after 10 minutes and 30 minutes.
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- - Storage conditions: Controlled room temperature (15-25°C, ≤70% relative humidity), protected from light and humidity (stored in a tightly closed container)
- Radiolabelling:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- Since the test item itself cannot be determined by a suitable analytical method, the samples were analysed for the tentantive hydrolysis product LZ 399. The analysis of LZ 399 was carried out by GC/FID detection - using matrix matched standards - after saturation of the samples with an excess of sodium chloride and extraction with ethylacetate.
- Buffers:
- - pH 4: Mixture of 360 mL of 0.1 M sodium hydroxide, 2000 mL of 0.1 M potassium citrate and 1640 mL of water. Measured pH value: 4.09
- pH 7: Mixture of 1184 mL of 0.1 M sodium hydroxide, 2000 mL of 0.1 M potassium dihydrogenphosphate and 816 mL of water. Measured pH value: 6.99
- pH 9: Mixture of 825 mL of 0.1 M sodium hydroxide, 2000 mL of boric acid and 1148 mL of water. Measured pH value: 8.98 - Details on test conditions:
- Since the test item was expected to hydrolyze rather fast, the conditions of the preliminary test were modified from the conditions given in the guideline. The test was carried out at 20 °C ± 0.5 °C. Samples of the test item in buffer solution pH 4, pH 7 and pH 9 were prepared and incubated for 30 minutes. Samples were taken immediately after preparation, after 10 minutes and 30 minutes.
- Duration:
- 30 min
- pH:
- 4
- Temp.:
- 20 °C
- Initial conc. measured:
- ca. 22 mg/L
- Duration:
- 30 min
- pH:
- 7
- Temp.:
- 20 °C
- Initial conc. measured:
- ca. 22 mg/L
- Duration:
- 30 min
- pH:
- 9
- Temp.:
- 30 °C
- Initial conc. measured:
- ca. 22 mg/L
- Number of replicates:
- test was carried out in duplicate
- Positive controls:
- no
- Negative controls:
- no
- Statistical methods:
- no statistics
- Preliminary study:
- The test item is not stable in aqueous buffer pH 4, 7 and 9 and immediately hydrolyses completely into LZ 399. Thus, the half-life time for hydolytical degradation is < 1 minute for buffer solutions at pH 4, 7 and 9.
- Test performance:
- The test was carried out at 20 °C ± 0.5 °C. Samples of the test item in buffer solution pH 4, pH 7 and pH 9 were prepared and incubated for 30 minutes. Samples were taken immediately after preparation, after 10 minutes and 30 minutes.
- Transformation products:
- yes
- No.:
- #1
- Details on hydrolysis and appearance of transformation product(s):
- The test item is not stable in aqueous buffer pH 4, 7 and 9 and immediately hydrolyses completely into LZ 399. Thus, the half-life time for hydolytical degradation is < 1 minute for buffer solutions at pH 4, 7 and 9.
- % Recovery:
- 0
- pH:
- 4
- Temp.:
- 20 °C
- Duration:
- 30 min
- Remarks on result:
- other: t1/2 = < 1 minute
- % Recovery:
- 0
- pH:
- 7
- Temp.:
- 20 °C
- Duration:
- 30 min
- Remarks on result:
- other: t1/2 = < 1 minute
- % Recovery:
- 0
- pH:
- 9
- Temp.:
- 20 °C
- Duration:
- 30 min
- Remarks on result:
- other: t1/2 = < 1 minute
- Key result
- pH:
- 4
- Temp.:
- 20 °C
- DT50:
- < 1 min
- Remarks on result:
- other: hydrolytically unstable
- Key result
- pH:
- 7
- Temp.:
- 20 °C
- DT50:
- < 1 min
- Remarks on result:
- other: hydrolytically unstable
- Key result
- pH:
- 9
- Temp.:
- 20 °C
- DT50:
- < 1 min
- Remarks on result:
- other: hydrolytically unstable
- Details on results:
- The test item is not stable in aqueous buffer pH 4, 7 and 9 and immediately hydrolyses completely into LZ 399. Thus, the half-life time for hydolytical degradation is < 1 minute for buffer solutions at pH 4, 7 and 9.
- Results with reference substance:
- no reference substance tested
- Validity criteria fulfilled:
- yes
- Conclusions:
- The test item is not stable in aqueous buffer pH 4, 7 and 9 and immediately hydrolyses completely into LZ 399. Thus, the half-life time for hydrolytical degradation is < 1 minute for buffer solutions at pH 4, 7 and 9. Therefore, no main study had to be performed.
- Executive summary:
In this study the hydrolysis was determined based on the OECD Guideline no. 111. Since the test item was expected to hydrolyze rather fast, a preliminary test with conditions modified from the conditions given in the guideline, was carried out. The test was carried out at 20 °C ± 0.5 °C. Samples of the test item in buffer solution pH 4, pH 7 and pH 9 were prepared and incubated for 30 minutes. Samples were taken immediately after preparation, after 10 minutes and 30 minutes. Since the test item itself cannot be determined by a suitable analytical method, the samples were analysed for the tentantive hydrolysis product LZ 399. The analysis of LZ 399 was carried out by GC/FID detection - using matrix matched standards - after saturation of the samples with an excess of sodium chloride and extraction with ethylacetate.
The test item is not stable in aqueous buffer pH 4, 7 and 9 and immediately hydrolyses completely into LZ 399. Thus, the half-life time for hydrolytical degradation is < 1 minute for buffer solutions at pH 4, 7 and 9. Therefore, no main study had to be performed.
Reference
Description of key information
In this study the hydrolysis was determined based on the OECD Guideline no. 111. Since the test item was expected to hydrolyze rather fast, a preliminary test with conditions modified from the conditions given in the guideline, was carried out. The test was carried out at 20 °C ± 0.5 °C. Samples of the test item in buffer solution pH 4, pH 7 and pH 9 were prepared and incubated for 30 minutes. Samples were taken immediately after preparation, after 10 minutes and 30 minutes. Since the test item itself cannot be determined by a suitable analytical method, the samples were analysed for the tentantive hydrolysis product LZ 399. The analysis of LZ 399 was carried out by GC/FID detection - using matrix matched standards - after saturation of the samples with an excess of sodium chloride and extraction with ethylacetate.
The test item is not stable in aqueous buffer pH 4, 7 and 9 and immediately hydrolyses completely into LZ 399. Thus, the half-life time for hydrolytical degradation is < 1 minute for buffer solutions at pH 4, 7 and 9. Therefore, no main study had to be performed.
Key value for chemical safety assessment
- Half-life for hydrolysis:
- 1 min
- 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.
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