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EC number: 203-389-7 | CAS number: 106-36-5
- 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
Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
Description of key information
The test material is readily biodegradable.
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
Additional information
The ready biodegradability of n-propyl propionate was evaluated according to the OECD Guideline301D: Closed Bottle Test. This test examined biodegradation of the test chemical (3 mg/L) in adefined mineral medium after inoculation (3 mL/Liter) with secondary effluent from the City of
Midland, Michigan Wastewater Treatment Plant. Consumption of dissolved oxygen in replicateinoculum blanks (no test substance added) and test chemical suspensions was determined after 5, 7,10, 14, 21, and 28 days incubation at an average temperature (± 1 Standard Deviation) of 20.1 ±
0.4 °C. Average net oxygen consumption in the test suspensions, corrected for oxygen consumed inthe inoculum blanks, was equivalent to 32.2, 56.8, 56.5, 60.0, 64.9, and 64.0% of the theoreticaloxygen demand (ThOD) after 5, 7, 10, 14, 21, and 28 days, respectively. Since the time required to
achieve >10% biodegradation (i.e. lag period) was less than 5 days, a precise determination of the 10 -day window following this onset could not be made. However, the test chemical achieved 60.0%biodegradation within the first 14 days of the test. Therefore, n-propyl propionate can be considered
as “readily biodegradable” according to current OECD criteria for the Closed Bottle Test.
The reference compound, sodium benzoate (4 mg/L), achieved > 60% biodegradation (i.e. 76.6± 0.7%) after 14 days. Consumption of dissolved oxygen in the inoculum blanks did not exceed0.68 mg/L over the 28 day test. With the exception of day 5 determinations, the difference of extremes
in percent biodegradation among replicate test suspensions did not exceed 20% at any of the samplingintervals. Therefore, the results of this test met each of the validation criteria established for theOECD Closed Bottle Test.
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