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EC number: 276-431-5 | CAS number: 72162-23-3 The high-boiling fraction separated by distillation from the products obtained from the reaction of nitric acid with cyclododecanol and cyclododecanone. Composed primarily of dodecanedioic acid, undecanedioic acid, and sebacic acid.
- 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
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
Description of key information
Assessing the toxicity to aquatic invertebrates, Daphnia magna was exposed to Corfree® M1 for 48 hours. The experiment was conducted according to OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test). The test gave a 48-h EC50 value of greater than 120 mg/L.
Key value for chemical safety assessment
Additional information
The acute toxicity of Corfree® M1 (also known as H-25313) to unfed Daphnia magna neonates, less than 24 hours old at test start, was determined in an unaerated, 48-hour, static test. The test was conducted in accordance with the Organisation for Economic Co-Operation and Development (OECD) Guideline for Testing Chemicals: 202; the European Economic Community 92/69 Annex V - Method C.2; and the United States Environmental Protection Agency, Office of Toxic Substances.
The study was conducted with five concentrations of H-25313 and a dilution water control at a mean temperature of 20.6°C (range of 20.2-20.9°C). Four replicates with 5 daphnids per replicate were used per test substance concentration and control. Exposure of daphnids to nominal H-25313 concentrations of 7.5, 15, 30, 60, and 120 mg/L resulted in 0, 5, 0, 0, and 0% immobility, respectively, at the end of 48 hours. No immobility was observed in the water control daphnids. The highest nominal concentration causing no immobility at test end was 120 mg/L. The lowest nominal concentration causing 100% immobility at test end was greater than 120 mg/L. The 48-hour EC50, based on nominal concentrations of H-25313 and immobility, was greater than 120 mg/L.
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