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EC number: 827-277-8 | CAS number: 1771689-37-2
- 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
Endpoint summary
Administrative data
Description of key information
Ready biodegradability
Key, OECD 301 F, GLP, 0.4% in 28 days: not readily biodegradable
Additional information
Ready biodegradability
The ready biodegradability test of the test item was conducted with unacclimatised sewage micro-organisms by measuring oxygen consumption over the 28-day test period according to OECD 301F and under GLP conditions.
The test item was added directly to test vessels at a level of 22.14 mg/L (equivalent to 53.35 mg/L as Theoretical Oxygen Demand or “ThODNH3”) (average, 2 replicate). The test concentration of sodium benzoate, used as reference substance in the Procedure Control, was 30.86 mg/L (equivalent to 51.54 mg/L as ThOD). In the Toxicity Control (TC) containing both test item and reference substance, the test item was added to the test vessel at a level of 22.09 mg/L(equivalent to 53.24 mg/L as ThODNH3) and the reference substance was added at a level of 31.75 mg/L of sodium benzoate (equivalent to 53.02 mg/L as ThOD). The concentration expressed as total ThOD was 106.26 mg/L. In the Abiotic Sterile Control (ASC), test vessel without inocula addition and containing sterilising agent, the test item was added to the test vessel at a level of 22.26 mg/L (equivalent to 53.65 mg/L as ThODNH3).
The biodegradation of test item after 28 days averaged 0.4% (2 replicates). The test item did not exhibit a percentage biodegradation exceeding the pass level of 60% within the 28-day period.
The biodegradation of the reference substance (Sodium benzoate) attained 63.5% after Day 3, 97.8% after Day 14 and 103.7% after Day 28.
In the Toxicity Control (TC) test mixture, 47.3% degradation occurred within 14 days and the value exceeded 25% based on total ThOD, which indicated that the test item can be assumed to be not inhibitory under the conditions of this test.
In the Abiotic Sterile Control (ASC) test vessel, 10.4% degradation occurred after 28 days.
Based on the results, the percentage biodegradation of the test item within 28 days did not exceed the pass level of 60% ThOD. The test item did not meet the criteria for “ready biodegradability” under the described test conditions.
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