Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 266-582-5 | CAS number: 67124-09-8
- 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
Sediment toxicity
Administrative data
Link to relevant study record(s)
Description of key information
Sediment-water chironomid test (OECD218): EC50(28d) > 560 mg/kg - based on developmental rate / EC50(28d): 380 mg/kg, NOEC: 180 mg/kg - based on reduction in emergence
Key value for chemical safety assessment
- EC50 or LC50 for freshwater sediment:
- 380 mg/kg sediment dw
- EC10, LC10 or NOEC for freshwater sediment:
- 180 mg/kg sediment dw
Additional information
The toxicity to sediment-water chironomid of the test substance was investigated according to OECD guideline 218 in a static mode with Chironimus riparius as test organisms, which are representative of a wide variety of natural habitats and can therefore be considered as important non-target organisms in freshwater ecosystems (Sewell and McKenzie, 2005).Following two preliminary range-finding test, four replicates of 20 larvae per concentration were exposed to formulated sediment spiked with test material at concentrations of 100, 180, 320, 560 and 1000 mg/kg (dry weight of sediment) for a period of 28 days. 600 mL glass beakers with approximately 8 cm in diameter were used. After the 2-day equilibration period the aeration was stopped and 20 larvae were placed in each test and control vessel and maintained in a temperature controlled room at approximately 21 °C with a photoperiod of 16 hours light and 8 hours darkness with 20 minute dawn and dusk transition periods. The aeration was switched back on after approximately 24 hours having allowed the larvae to settle in the sediment. The larvae were fed at a rate of 0.5 mg Tetramin® flake food per larva per day. The Tetramin® flake food was prepared as a suspension in water and an appropriate volume added to the overlying water. The measured end-point for the test was the number of live, emerged adult midges. The number of emerged adult midges was recorded daily until termination of the study after 28 days. The sex of the individual midges was also determined after emergence. The male midges were identified
by the presence of plumose antennae and the female by the absence of plumose antennae. Any egg masses produced prior to termination were also recorded and removed fiom the test vessels to prevent re-introduction of larvae into the sediment. The number of visible pupae that failed to emerge were counted separately. Any abnormal behaviour was also recorded. The control group was maintained under identical conditions but not exposed to the test material. The EC50 (development rate) based on nominal test concentrations was greater than 560 mg/kg. Although significantly lower numbers of adult midges emerged at the concentration of 560 mg/kg, the rate at which they emerged was similar to that of the control, therefore the EC50 (development rate) was greater than 560 mg/kg. No adult midges emerged at 1000 mg/kg, therefore a calculated EC50 value could not be determined. The 28-Day EC50 (reduction in emergence) based on nominal test concentrations was 380 mg/kg with 95 % confidence limits of 300 - 490 mg/kg. The No Observed Effect Concentration (NOEC) was 180 mg/ kg. Analysis of the test sediments on Day -2, 0 and 28 showed the measured concentrations to range from 84 % to 119 % of nominal. Therefore it was considered justifiable to calculate the results based on nominal test concentrations only. The study is regarded as well-documented Guideline study with certificated GLP compliance and is therefore referred as "key study" without restrictions (Klimisch 1).
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.