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EC number: 230-525-2 | CAS number: 7173-51-5
- 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:
- 27 Feb, 1997 - 10 Mar, 1997
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.7 (Degradation: Abiotic Degradation: Hydrolysis as a Function of pH)
- Version / remarks:
- Cited as Directive 84/449/EEC, C.10
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- At each sampling time 25 mL of sample was taken with a pipette and transferred into a 250 mL beaker. The samples were stored in the refrigerator or immediately subjected to the analytical procedure. The temperature of the thermostatic water bath was checked at least at the start and end of the tests and at each sampling time.
- Buffers:
- pH = 4.0: 100 mL of 0.5 M potassium hydrogen phtalate and 0.8 mL 0.5 M NaOH made up to 1 L with deionized water
pH = 7.0: 100 mL of 0.5 M potassium hydrogen phosphate and 5.92 mL 5 M NaOH made up to 1 L with deionized water
pH = 9.0: 100 mL of 0.5 M boric acid, 100 mL of 0.5 M potassium chloride and 100 mL 4.32 M NaOH made up to 1 L with deionized water - Details on test conditions:
- -Temperature: 49.9 – 50.1°C
-pH: 4,7 and 9 and the pH changes were always less than 0.05 pH units for each level
-Duration of the test: 7220 min (= 120 h = 5 d)
- Number of replicates:2 - Duration:
- 120 h
- pH:
- 4
- Temp.:
- 50 °C
- Initial conc. measured:
- ca. 3.509 mg/L
- Duration:
- 120 h
- pH:
- 7
- Temp.:
- 50 °C
- Initial conc. measured:
- ca. 3.939 mg/L
- Duration:
- 120 h
- pH:
- 9
- Temp.:
- 50 °C
- Initial conc. measured:
- ca. 2.68 mg/L
- Number of replicates:
- 2 at pH 4 and 7 and 4 at pH 9
- Preliminary study:
- Yes, preliminary test was also definite test because of the outcome.
- Transformation products:
- not specified
- Key result
- pH:
- 4
- Temp.:
- 20 °C
- DT50:
- >= 1 yr
- Key result
- pH:
- 7
- Temp.:
- 20 °C
- DT50:
- >= 1 yr
- Key result
- pH:
- 9
- Temp.:
- 20 °C
- DT50:
- >= 1 yr
- Validity criteria fulfilled:
- yes
- Conclusions:
- The substance is hydrolytically stable, with a DT50 equal to or greater than one year.
- Executive summary:
The hydrolytic stability of the test substance was determined according to EU Method C7.The substance was kept in buffer solutions at pH 4.0, 7.0 and 9.0 in a water bath at 50°C for 5 days. Samples were taken at test start, then at regular intervals afterwards to determine half-life. If t1/2 was less than 2.4 h, or if less than 10% of the test substance was hydrolysed in 5 days, then no further test needed to be performed at that pH.The test substance showed less than 10% degradation after 5 days at 50°C for all three pH values. It was therefore considered hydrolytically stable at pH 4.0, 7.0 and 9.0, with a half-life equal to or greater than one year at ambient temperature (Geurts and Van Wijk, 1997).
Reference
The test material showed less than 10% degradation after five days at 50 deg.C in all three tested pH. It is concluded that DDAC is hydrolytically stable at pH 4.0, 7.0 and 9.0 with a half-life equal or greater than a year at ambient temperatures.
Description of key information
Key value for chemical safety assessment
- Half-life for hydrolysis:
- 1 yr
- at the temperature of:
- 20 °C
Additional information
The hydrolytic stability of the test substance was determined according to EU Method C7. The substance was kept in buffer solutions at pH 4.0, 7.0 and 9.0 in a water bath at 50°C for 5 days. Samples were taken at test start, then at regular intervals afterwards to determine half-life. If t1/2 was less than 2.4 h, or if less than 10% of the test substance was hydrolysed in 5 days, then no further test needed to be performed at that pH. The test substance showed less than 10% degradation after 5 days at 50°C for all three pH values. It was therefore considered hydrolytically stable at pH 4.0, 7.0 and 9.0, with a half-life equal to or greater than one year at ambient temperature (Geurts and van Wijk, 1997).
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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