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Diss Factsheets
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EC number: 204-009-2 | CAS number: 112-84-5
- 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
Bioaccumulation: aquatic / sediment
Administrative data
Link to relevant study record(s)
Description of key information
Meylan et al. (1999) methodology updated with the Arnot and Gobas’ database (2008) uses different equations depending on the partition coefficient of the chemical. This QSAR is considered relevant for the estimation of the BCF of amides. The QSAR estimates that Erucamide is not a “B” substance. A worst case BCF based on no biotransformation estimates a BCF of 1893 L/Kg. All other estimates ore considerably lower: 659.9 estimated by Mehlan or less than 100 for 3 other QSARs.
Key value for chemical safety assessment
Additional information
Based on the different QSAR predictions, Meylan et al.(1999) methodology updated with the Arnot and Gobas’ database (2008) uses different equations depending on the partition coefficient of the chemical. The QSAR is considered relevant for the estimation of the BCF of amides. The in vitro study from Du Pont de Nemour (1997) indicated that there was no metabolite biotransformation in fish hepatocytes, but no information was provided on other mechanistic processes, such as chemical uptake from the water at the cell membrane surface and chemical elimination at the membrane surface. These processes and others (e.g. faecal egestion and growth dilution) are included in the Arnot-Gobas model and this QSAR estimates that Erucamide is not a “B” substance. As water solubility is extremely low (<1 µg/L) it is also possible that bioavailablity to the hepatocytes may not have been high enough in the test for the cells to absorb the substance and to demonstrate significant metabolism.
Equations from Arnot and Gobas would conclude that high bioaccumulation potential is likely if no biotransformation is assumed. But evidence from alkenes and acid surrogates show that metabolism should not be ignored for amides. In this case it can be concluded that Erucamide is not a “B” substance according to this QSAR.
Overall, Erucamide would not be a “B” substance in this assessment however a more pecise estimate of BCF cannot be provided. Due to technical difficulties it is not currently possible to perform a BCF study.
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