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EC number: 219-941-5 | CAS number: 2579-20-6
- 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:
- 12 November 1999 to 10 January 2000
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP study conducted according to OECD guideline.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 111 (Hydrolysis as a Function of pH)
- GLP compliance:
- yes (incl. QA statement)
- Radiolabelling:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- - Sampling intervals for the parent/transformation products: 0, 2.4, and 120 hours
- Sampling method: GC
- Sampling intervals/times for pH measurements: various times
- Sampling intervals/times for sterility check: not specified
- Sample storage conditions before analysis: pH 4, 7, 9 at 50.0±0.5°C for five days. - Buffers:
- - pH: 4
- Type and final molarity of buffer: (0.05, 0.10, 0.05 mol/l)
- Composition of buffer: Citric acid, sodium hydroxide, hydrochloric acid
- pH: 7
- Type and final molarity of buffer: (0.04, 0.03 mol/l)
- Composition of buffer: disodium hydrogen phosphate, potassium dihydrogen phosphate
- pH: 9
- Type and final molarity of buffer: (0.05, 0.02 mol/l)
- Composition of buffer: disodium tetraborate, hydrochloric acid - Details on test conditions:
- TEST SYSTEM
- Type, material and volume of test flasks, other equipment used: stoppered glass flasks
- Sterilisation method: Buffer solutions were filtered through a 0.2 micrometer membrane filter to ensure they were sterile before commencement of the test.
- Measures taken to avoid photolytic effects: sheilded from light
- Measures to exclude oxygen: Solutions were subjected to ultrasonication and degassing with nitrogen to minimise dissolved oxygen content.
TEST MEDIUM
- Volume used/treatment: sample solutions were prepared at nomial concentration of 0.2g/l in the buffer solutions. - Duration:
- 120 h
- pH:
- 4
- Initial conc. measured:
- 188 mg/L
- Duration:
- 120 h
- pH:
- 9
- Initial conc. measured:
- 176 mg/L
- Duration:
- 120 h
- pH:
- 7
- Initial conc. measured:
- 196 mg/L
- Number of replicates:
- 3
- Transformation products:
- no
- % Recovery:
- 98
- pH:
- 4
- Temp.:
- 50 °C
- Duration:
- 120 h
- % Recovery:
- 97
- pH:
- 7
- Temp.:
- 50 °C
- Duration:
- 120 h
- % Recovery:
- 100
- pH:
- 9
- Temp.:
- 50 °C
- Duration:
- 120 h
- pH:
- 4
- Temp.:
- 50 °C
- DT50:
- > 1 yr
- pH:
- 7
- Temp.:
- 50 °C
- DT50:
- > 1 yr
- pH:
- 9
- Temp.:
- 50 °C
- DT50:
- > 1 yr
- Details on results:
- TEST CONDITIONS
- pH, sterility, temperature, and other experimental conditions maintained throughout the study: Yes - Validity criteria fulfilled:
- yes
- Conclusions:
- The estimated half-life at 25°C of 1,3-BAC at pH 4, 7 and 9 is greater than 1 year.
- Executive summary:
Assessment of hydrolytic stability was carried out using Method 111 of the OECD Guidelines for Testing of Chemicals, 12 May 1981. Sample solutions were prepared in stoppered glass flasks at a nominal concentration of 0.2 g/l in the three buffer solutions. The solutions were shielded from light whilst maintained at the test temperature. Sample solutions at pH 4, 7 and 9 were maintained at 50.0 ± 0.5°C for a period of 5 days. Less than 10% hydrolysis after 5 days at 50°C is equivalent to a half-life of greater than 1 year at 25°C at pH 4, 7, and 9. Therefore the estimated half-life at 25 ºC of 1,3 -BAC at pH 4, 7 and 9 is greater than 1 year.
Reference
Less than 10% hydrolysis after 5 days at 50°C, equivalent to a half-life of greater than 1 year at 25°C at pH 4, 7, and 9.
Description of key information
Less than 10% hydrolysis was seen after 5 days at 50°C, equivalent to a half-life of greater than 1 year at 25°C at pH 4, 7, and 9.
Key value for chemical safety assessment
- Half-life for hydrolysis:
- 1 yr
- at the temperature of:
- 25 °C
Additional information
Assessment of hydrolytic stability was carried out using Method 111 of the OECD Guidelines for Testing of Chemicals, 12 May 1981. Sample solutions were prepared in stoppered glass flasks at a nominal concentration of 0.2 g/l in the three buffer solutions. The solutions were shielded from light whilst maintained at the test temperature. Sample solutions at pH 4, 7 and 9 were maintained at 50.0 ± 0.5°C for a period of 5 days. Less than 10% hydrolysis after 5 days at 50°C, equivalent to a half-life of greater than 1 year at 25°C at pH 4, 7, and 9.
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