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Diss Factsheets
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EC number: 481-970-6 | 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
- Endpoint:
- hydrolysis
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 31st March 2007 to 1st May 2007
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: 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 relevant results
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 007
- Report date:
- 2007
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 111 (Hydrolysis as a Function of pH)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.7 (Degradation: Abiotic Degradation: Hydrolysis as a Function of pH)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- Date of inspection; 30th August 2005 Date of inspection: 21st November 2005
Test material
Reference
- Name:
- Unnamed
- Type:
- Constituent
- Details on test material:
- Sponsor's identification :C-C1
Description : dark blue powder
Lot number : MB-1
Date received : 05 March 2007
Storage conditions :room temperature in the dark, over silica gel
- Radiolabelling:
- no
Study design
- Analytical monitoring:
- yes
- Details on sampling:
- Preparation of samples
Sample solutions were prepared in stoppered glass flasks at a nominal concentration of 1 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
Sample solutions at pH 4, pH 7 and pH 9 were maintained at 50.0 ± 0.5°C for a period of 5 days
Analysis of sample solutions
The sample solutions were taken from the waterbath 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 4 using reverse osmosis water.
Standards
Duplicate standard solutions of test material were prepared in reverse osmosis water:buffer (3:1) at a nominal concentration of 250 mg/l.
Analysis - Buffers:
- Specification of buffer solutions
(pH) Components Concentration
(mol dm-3)
4 Potassium hydrogen phthalate 0.01
7 Disodium hydrogen orthophosphate (anhydrous) 0.006
Potassium dihydrogen orthophosphate 0.004
Sodium chloride 0.004
9 Disodium tetraborate 0.002
Sodium chloride 0.004
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. - Details on test conditions:
- TEST SYSTEM
- Type, material and volume of test flasks, other equipment used: not stated in report
Preliminary test
Sample solutions at pH 4, pH 7 and pH 9 were maintained at 50.0 ± 0.5°C for a period of 5 days.
The buffer solutions were filtered through a 0.2 µm membrane filter to ensure they were sterile before commencement of the test.
The linearity of the detector response with respect to concentration was assessed over the nominal concentration range of 0 to 508 mg/l. This was satisfactory with a correlation coefficient of 1.00 being obtained.
Duration of testopen allclose all
- Duration:
- 5 d
- pH:
- 9
- Initial conc. measured:
- 0.999 g/L
- Duration:
- 5 d
- pH:
- 9
- Initial conc. measured:
- 1 g/L
- Duration:
- 5 d
- pH:
- 7
- Initial conc. measured:
- 1 g/L
- Duration:
- 5 d
- pH:
- 7
- Initial conc. measured:
- 1.01 g/L
- Duration:
- 5 d
- pH:
- 4
- Initial conc. measured:
- 0.979 g/L
- Duration:
- 5 d
- pH:
- 4
- Initial conc. measured:
- 0.975 g/L
- Positive controls:
- no
- Negative controls:
- no
- Statistical methods:
- None
Results and discussion
- Preliminary study:
- Not applicable
- Test performance:
- The linearity of the detector response with respect to concentration was assessed over the nominal concentration range of 0 to 508 mg/l. This was satisfactory with a correlation coefficient of 1.00 being obtained.
- Transformation products:
- no
- Details on hydrolysis and appearance of transformation product(s):
- Not applicable
Total recovery of test substance (in %)open allclose all
- % Recovery:
- 97.9
- pH:
- 4
- Temp.:
- 50 °C
- Duration:
- 5 d
- % Recovery:
- 98.5
- pH:
- 4
- Temp.:
- 50 °C
- Duration:
- 5 d
- % Recovery:
- 98.4
- pH:
- 7
- Temp.:
- 50 °C
- Duration:
- 5 d
- % Recovery:
- 98.9
- pH:
- 7
- Temp.:
- 50 °C
- Duration:
- 5 d
- % Recovery:
- 101
- pH:
- 9
- Temp.:
- 50 °C
- Duration:
- 5 d
- % Recovery:
- 100
- pH:
- 9
- Temp.:
- 50 °C
- Duration:
- 5 d
Dissipation DT50 of parent compoundopen allclose all
- pH:
- 4
- Temp.:
- 50 °C
- DT50:
- > 8 760 h
- pH:
- 7
- Temp.:
- 50 °C
- DT50:
- > 8 760 h
- pH:
- 9
- Temp.:
- 50 °C
- DT50:
- > 8 760 h
- Details on results:
- pH 4: Less than 10% hydrolysis after 5 days at 50°C, equivalent to a half-life greater than 1 year at 25°C.
pH 7: Less than 10% hydrolysis after 5 days at 50°C, equivalent to a half-life greater than 1 year at 25°C.
pH 9: Less than 10% hydrolysis after 5 days at 50°C, equivalent to a half-life greater than 1 year at 25°C.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Remarks:
- The linearity of the detector response with respect to concentration was assessed over the nominal concentration range of 0 to 508 mg/l. This was satisfactory with a correlation coefficient of 1.00 being obtained.
- Conclusions:
- The estimated half-life at 25°C of the test material for pH 4, pH 7 and pH 9 has been shown to be >1 year.
- Executive summary:
The determination was carried out using Method C7 of Commission Directive 92/69/EEC and Method 111 of the OECD Guidelines for Testing of Chemicals, 13 April 2004.
The estimated half-life at 25°C of the test material for pH 4, pH 7 and pH 9 has been shown to be >1 year.
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