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EC number: 258-436-4 | CAS number: 53220-22-7
- 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
- Study period:
- 1989-09-01 to 1989-10-05
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 D (Ready Biodegradability: Closed Bottle Test)
- Version / remarks:
- 1982
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.6 (Degradation: Chemical Oxygen Demand)
- Version / remarks:
- 1984
- Deviations:
- no
- GLP compliance:
- yes
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, non-adapted
- Details on inoculum:
- - Source of inoculum/activated sludge: RZWI Nieuwgraaf in Duiven. The RZWI Nieuwgraaf in Duiven is an activated sludge plant treating predominantly domastic waste water.
- Laboratory culture: no
- Initial cell/biomass concentration: 2 mg DW/L - Duration of test (contact time):
- 28 d
- Initial conc.:
- 2 mg/L
- Based on:
- test mat.
- Initial conc.:
- 2.58 other: g O2/g
- Based on:
- ThOD
- Remarks:
- per L
- Parameter followed for biodegradation estimation:
- O2 consumption
- Remarks:
- The biodegradation was calculated as the ratio of the biochemical oxygen demand (BOD) to the theoretical oxygen demand (ThOD). The ThOD of the test substance (pure active ingredient) is 2.58 g O2/g test substance.
- Details on study design:
- TEST CONDITIONS
- Composition of medium: according to the guideline
- pH: 7.4 (end of the test)
TEST SYSTEM
- Culturing apparatus: 280 mL BOD (Biological Oxygen Demand) bottles
- Number of culture flasks/concentration: 2
- Stock solution: Sodium acetate was added to the bottle using stock solution of 1000 mg/L. For the application of the test substance on silica gel, a stock solution of 1000 mg/L in dichlormethane was added.
SAMPLING
- Sampling frequency: on day 0, 5, 15, 28
CONTROL AND BLANK SYSTEM
- Inoculum blank: yes
- Toxicity control: yes - Reference substance:
- acetic acid, sodium salt
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 65
- Sampling time:
- 28 d
- Details on results:
- The biodegradation rate reached 65% at the end of the test period. Therefore, the test item should be classified as readily biodegradable in this Closed-Bottle-Test.
- Results with reference substance:
- The biodegradation of the positive control sodium acetate was 94 % on day 28.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The ready biodegradability of the test item was assessed according to OECD guideline 301 D and EU-method C.6. The test item was biodegraded 65 % at day 28 in the Closed Bottle test. Therefore it can be concluded that the ditetradecyl peroxydicarbonate is readily biodegradable.
- Executive summary:
A ready biodegradability test of ditetradecyl peroxydicarbonatewas performed which allows the biodegradability to be measured in an aerobic aqueous medium. The ready biodegradability was determined in the Closed Bottle test performed according to OECD guideline no. 301 . The biodegradation rate reached 65% at the end of the test period. Therefore, the test item should be classified as readily biodegradable in this Closed Bottle Test. The test is valid as shown by an endogenous respiration of 0.4 mg/L and by the mineralization of the reference compound, sodium acetate (94 %).
Reference
Oxygen consumption (in mg O2/litre) after 5, 15 and 28 days:
- test substance: 5.1; 3.0; 3.4
- sodium acetate: 4.2; 4.6; 4.9
Percentages biodegradation (in % BOD/ThOD) after 5, 15, 28 days:
- test substance: 44; 58; 65
- sodium acetate: 81; 88; 94
The validity of the test is shown by the oxygen consumption in the control bottle with sodium acetate and and endogenous repiration of 0.4 mg/L. The pH of the medium at the end of the test period is 7.4.
Description of key information
The ready biodegradability of the test item was assessed according to OECD guideline 301 D and EU-method C.6. The test item was biodegraded 65 % at day 28 in the Closed Bottle test. Therefore it can be concluded that the test item is readily biodegradable.
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
- Type of water:
- freshwater
Additional information
A ready biodegradability test of ditetradecyl peroxydicarbonatewas performed which allows the biodegradability to be measured in an aerobic aqueous medium. The ready biodegradability was determined in the Closed Bottle test performed according to OECD guideline no. 301 . The biodegradation rate reached 65% at the end of the test period. Therefore, the test item should be classified as readily biodegradable in this Closed Bottle Test. The test is valid as shown by an endogenous respiration of 0.4 mg/L and by the mineralization of the reference compound, sodium acetate (94 %).
Furthermore the biodegradability of the read-across substance was assessed according to OECD guideline 301 D. The test item was biodegraded by 68 % at day 28 in the Closed Bottle test. Over 60 % biodegradation was achieved in a period of less than 12 days immediately following the attainment of 10 % biodegradation. Hence the read across substance was classified as readily biodegradable, too.
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