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EC number: 810-149-0 | CAS number: 1050477-43-4
- 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:
- supporting study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.4-D (Determination of the "Ready" Biodegradability - Manometric Respirometry Test)
- Deviations:
- no
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
- Deviations:
- not applicable
- GLP compliance:
- yes (incl. QA statement)
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic (adaptation not specified)
- Details on inoculum:
- Type: mixed population of aquatic microorganisms (activated sludge)
Origin: aeration tank of a wastewater plant treating predominantly domestic sewage (Wupper area water authority, WWTP Odenthal)
Date of collection: 2016-07-04
Concentration of inoculum: 30 mg/L suspended solids
Pre-treatment of the inoculum
− Before use, the inoculum was stored at room temperature under continuous stirring with aeration.
− One day before start of the test the sludge was washed twice by adding mineral medium and centrifuging for 10 min at 2000 rpm and 20 °C and decanting off the supernatant.
− An aliquot of the wet sludge was dried in order to determine the wet weight / dry weight ratio of the sludge and to prepare a stock suspension (activated sludge) of 3 g dw/L.
− The calculated amount of sludge, needed to achieve 300 mL of this stock suspension, was dissolved in mineral medium and then filled up to a defined end volume. The suspension was stored again at room temperature under continuous stirring with aeration until start of the study the next day. Evaporated mineral medium was replaced. - Duration of test (contact time):
- 28 d
- Initial conc.:
- 100 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- Pre-treatment of the test item
- 25 mg of CN-Ethyl-TH-naphthyridinon were weighed out and added to the test flasks, filled with 200 mL of mineral medium
- the volume was made up to 250 mL with mineral medium containing the inoculum to give a test concentration of 100 mg test item/L
Pre-treatment of the reference compound
Reference compound name : sodium benzoate (Acros Organics)
Coding number : Ökotox_7/02
Purity : 99.9 %
Batch-no. : A0357641
Expiry date : 2018-03-27
- 25 mg of the reference compound were weighed out and added to the test flasks, filled with 200 mL of mineral medium
- the volume was made up to 250 mL with mineral medium containing the inoculum to give a test concentration of 100 mg reference compound /L
Pre-treatment of the toxicity control
- 25 mg of the test item and 25 mg of the reference compound were weighed out and added to the test flasks, filled with 200 mL of mineral medium
-volume was made up to 250 mL with mineral medium containing the inoculum to give a test concentration of 100 mg test item and reference compound/L
Exposure conditions
- Test volume: 250 mL
- Test apparatus OxiTopControl System (WTW)
- Mixing: 1 magnetic stirrer per test vessel
- Incubation time: 28 days
- Incubation temperature: 22 ± 1 °C
- Determinations of test item and inoculum blank were carried out in triplicate and of reference compound in duplicate - Reference substance:
- benzoic acid, sodium salt
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 0
- Sampling time:
- 28 d
- Parameter:
- % degradation (O2 consumption)
- Value:
- 0
- Sampling time:
- 7 d
- Parameter:
- % degradation (O2 consumption)
- Value:
- 1
- Sampling time:
- 14 d
- Parameter:
- % degradation (O2 consumption)
- Value:
- 1
- Sampling time:
- 21 d
- Details on results:
- The oxygen consumed by nitrification was not determined after 28 days, because no degradation of the test item was observed.
- Results with reference substance:
- The reference compound sodium benzoate showed 69 % degradation after 14 days.
- Validity criteria fulfilled:
- yes
- Remarks:
- reference compound reached the level of ≥ 60 percent for ready biodegradability within 14 days; toxicity control exhibited degradation rates > 25 % within 14 days; oxygen uptake of the inoculum blank was ≤ 60 mg/L
- Interpretation of results:
- not readily biodegradable
- Conclusions:
- CN-ethyl-TH-naphthyridinon showed 0 % degradation after 28 days. The reference compound sodium benzoate showed 69 % degradation after 14 days. Therefore, CN-ethyl-TH-naphthyridinon is considered to be “Not Readily Biodegradable“.
- Executive summary:
The study was conducted in accordance with the Council Regulation (EC) No 440/2008, Method C.4-D “Manometric Respirometry Test“(2008). This test method is in all essential parts identical with OECD Guideline 301 F (adopted July 1992). A suspension of CN-ethyl-TH-naphthyridinon in a mineral medium was inoculated and incubated for 28 d under aerobic conditions. During this period, degradation was followed by continuous automated BOD determinations. The reference compound sodium benzoate showed 69 % degradation after 14 days. CN-ethyl-TH-naphthyridinon showed 0 % degradation after 28 days. Therefore, CN-ethyl-TH-naphthyridinon is considered to be “Not Readily Biodegradable“.
Reference
The pH-values after 28 days were measured to be between 7.3 -7.9.
Description of key information
The study was conducted in accordance with the test method EC C.4-D “Manometric Respirometry Test“(2008), which is in all essential parts identical with OECD Guideline 301 F. A suspension of CN-ethyl-TH-naphthyridinon in a mineral medium was inoculated and incubated for 28 d under aerobic conditions. The reference compound sodium benzoate showed 69 % degradation after 14 days.
CN-ethyl-TH-naphthyridinon showed 0 % degradation after 28 days. Therefore, CN-ethyl-TH-naphthyridinon is considered to be “Not Readily Biodegradable“.
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.
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