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Diss Factsheets
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EC number: 500-230-6 | CAS number: 68698-70-4
- 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
Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 D (Ready Biodegradability: Closed Bottle Test)
- GLP compliance:
- yes (incl. QA statement)
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, non-adapted
- Details on inoculum:
- The inoculum was prepared from a secondary effluent obtained from Peppers Ferry Wastewater Treatment Plant (Blacksburg, Virginia).
- Duration of test (contact time):
- 28 d
- Initial conc.:
- 30 mg/L
- Based on:
- test mat.
- Initial conc.:
- 75 mg/L
- Based on:
- ThOD
- Parameter followed for biodegradation estimation:
- CO2 evolution
- Details on study design:
- A standard constant-pressure respirometer was used to measure oxygen consumption. There were seven flasks as follows: two flasks contained inoculum (“Blank”); two flasks contained inoculum and test material (“Test”); one flask contained a reference substance and inoculum (“Ref”); one flask contained inoculum with test material and the reference substance (“Tox”); one flask contained test material and a sterilizing agent (“Sterile”).
A small open container of soda lime pellets in each flask removed evolved CO2 from the gas phase. Each flask was gently stirred continuously using a magnetic stirrer. Volume-change readings were made at least daily in the testing apparatus. Re-establishment of equilibrium was performed as needed. Gas volume changes in test and reference flasks were compared to volume changes in the blanks to determine net oxygen consumption in the test chambers.
Test Environment
The test system was located in a secure area and was maintained at 22 ± 1 °C in near-darkness for the duration of the test.
Test Chronology
Testing proceeded as described in OECD 301F guidelines. Measurements of oxygen consumption were made daily. As oxygen consumption proceeded and/or atmospheric pressure changed, the cumulative volume change over those days was measured.
Re-establishment of equilibrium (reset) was performed at least daily, and more often when the extreme ranges of the graduated device were neared. - Reference substance:
- acetic acid, sodium salt
- Parameter:
- % degradation (O2 consumption)
- Value:
- 7.7
- Sampling time:
- 10 d
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 7.9
- Sampling time:
- 20 d
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 8.3
- Sampling time:
- 28 d
- Details on results:
- The DEAPA/AEP Epoxy Resin Adduct 10-day window of degradation did not open within the study period. The product reached a maximum of 8.3% by test termination.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- not readily biodegradable
- Conclusions:
- The 4,4'-Isopropylidenediphenol, oligomeric reaction products with 1-chloro-2,3-epoxypropane, reaction products with 3-aminopropyldiethylamine and 2-piperazin-1-ylethylamine not reach pass levels for biodegradation within the 28-day period of the test, indicating that it is not readily biodegradable. The toxicity control treatment reached pass levels for biodegradation by day 7, indicating that the test substance is not inhibitory.
- Executive summary:
The 4,4'-Isopropylidenediphenol, oligomeric reaction products with 1-chloro-2,3-epoxypropane, reaction products with 3-aminopropyldiethylamine and 2-piperazin-1-ylethylamine not reach pass levels for biodegradation within the 28-day period of the test, indicating that it is not readily biodegradable. The toxicity control treatment reached pass levels for biodegradation by day 7, indicating that the test substance is not inhibitory.
Reference
Description of key information
The 4,4'-Isopropylidenediphenol, oligomeric reaction products with 1-chloro-2,3-epoxypropane, reaction products with 3-aminopropyldiethylamine and 2-piperazin-1-ylethylamine not reach pass levels for biodegradation within the 28-day period of the test, indicating that it is not readily biodegradable. The toxicity control treatment reached pass levels for biodegradation by day 7, indicating that the test substance is not inhibitory.
Key value for chemical safety assessment
- Biodegradation in water:
- under test conditions no biodegradation observed
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.