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EC number: 219-470-5 | CAS number: 2440-22-4
- 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
Toxicity to soil macroorganisms except arthropods
Administrative data
Link to relevant study record(s)
Description of key information
No toxic effects could be observed in a study with Eisenia fetida.
Key value for chemical safety assessment
Additional information
In a 56-day study, adult earthworms of the species Eisenia fetida were exposed to the test substance in concentrations of 62.5, 125, 250, 500 and 1000 mg/kg soil dry weight, in accordance with the OECD 222 guideline. The mortality and the body weight change of the adult worms were observed and recorded on day 28. The reproduction, number of juveniles per test vessel 56 days after application was observed.
Adult worms:
No mortality of adult worms was observed in the controls and at all replicates with
test substance
NOECMortality: ≥ 1000 mg test substance/kg soil (dw)
LOECMortality: > 1000 mg test substance /kg soil (dw).
NOECBiomass change: ≥ 1000 mg test substance/kg soil (dw)
LOECBiomass change: > 1000 mg test substance /kg soil (dw)
Juvenile worms:
Reproduction by count of juvenile worms:
NOECReproduction: ≥ 1000 mg test substance/kg soil (dw)
LOECReproduction: > 1000 mg test substance/kg soil (dw)
No ECx calculations were performed, because there was no dose response relationship. A significant effect was observed at 500 mg/kg of test substances (Wilcoxon test, one sided -; p ≤0.05). However, this can be disregarded as the highest concentration (1000 mg/kg test substance/kg soil (dw)) and a lower concentration than this (125 mg/kg test substance/kg soil (dw)) showed similar number of offspring which is the range of reproduction in control assays. Therefore, we can conclude that this observation is an outlier.
The results in this study are consistent with all relevant validity criteria and the test is valid according to the test guideline of this study. No deviations from the test guidelines or other incidents occurred during the reported test, which may have influenced the results.
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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