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Diss Factsheets
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EC number: 210-236-8 | CAS number: 610-81-1
- 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
Toxicity to aquatic plants other than algae
Administrative data
Link to relevant study record(s)
Description of key information
The 7-day ErC50 was calculated to be 10.1 (95% CI: 9.7-10.5) and 8.10 (95% CI: 7.93-8.27) mg test item/L for frond number and dry weight, respectively.
The 7-day ErC10 was calculated to be 3.18 (95% CI: 2.95-3.42) and 2.82 (95% CI: 2.70-2.95) mg test item/L for frond number and dry weight, respectively.
Key value for chemical safety assessment
Additional information
The purpose of this study was to determine the inhibitory effect of the test item on the growth of the freshwater aquatic plant Lemna gibba, according to OECD 221 guideline and following the GLP. For this purpose, cultures of Lemna gibba were exposed in a semi-static test with daily water renewal to various concentrations under defined conditions: 80, 25, 8.0, 2.5 and 0.8 mg test item/L and a control; corresponding to the following geometric mean measured concentrations: 27.8, 8.49, 3.91, 1.26, 0.428 mg test item/L. This study encompassed 6 treatment groups (5 dose rates of the test item and a control) with three replicates per test concentration and control. At test start 12 fronds were introduced in each replicate and incubated for 7 days. The frond numbers were determined on day 2, 5 and 7. The dry weight of each replicate was determined at test termination. The 7-day ErC50 was calculated to be 10.1 and 8.10 mg test item/L for frond number and dry weight, respectively. The 7-day ErC10 was calculated to be 3.18 and 2.82 mg test item/L for frond number and dry weight, respectively. All reported results refer to geometric mean concentrations, since the test item concentrations were not within ± 20% of the nominal concentrations during the test. All the validity criteria were fulfilled accordingto the OECD guideline 221.
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