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EC number: 247-148-4 | CAS number: 25637-99-4
- 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
Long-term toxicity to fish
Administrative data
Link to relevant study record(s)
Description of key information
The following information is available for this endpoint:
Drottar, K. R., MacGregor, J. A. and Krueger, H. O. (2001). Hexabromocyclododecane (HBCD): An early life-stage toxicity test with the Rainbow Trout (Oncorhynchus mykiss). Report no.: 439A-112. Report date: 2001-07-12.
Ronisz, D., Farmen Finne, E., Karlsson, H. and Förlin, L. (2004). Effects of the brominated flame retardants hexabromocyclododecane (HBCDD), and tetrabromobisphenol A (TBBPA), on hepatic enzymes and other biomarkers in juvenile rainbow trout and feral eelpout. Aquatic Toxicology (2004), Vol. 69, pp.229-245.
Kuiper, R. V., Cantón, R. F., Leonards, P. E. G., Jenssen, B. M., Dubbeldam, M., Wester, P. W., van den Berg, M., Vos, J. G. and Vethaak, A. D. (2007). Long-term exposure of European flounder (Platichthys flesus) to the flame-retardants tetrabromobisphenol A (TBBPA) and hexabromocyclododecane (HBCD). Ecotoxicology and Environmental Safety (2007), Vol. 67, pp. 349-360.
Drottar et al. (2001) is the key study for this endpoint. This study was conducted in accordance with recognised testing guidelines and under conditions of GLP and was allocated a reliability score of 1 according to the criteria set out by Klimisch et al. (1997).
Ronisz et al. (2004) and Kuiper et al. (2007) , were both allocated a reliability score of 4 according to the criteria set out by Klimisch et al. (1997).
Key value for chemical safety assessment
Additional information
The GLP/guideline compliant fish early life stage test in rainbow trout (Oncorhynchus mykiss) was performed at doses which were multiples of the gamma diasteromer's water solubility, e.g. eggs were exposed to nominal test concentrations of 0, 0.43, 0.85, 1.7, 3.4 and 6.8 µg/l (measured concentrations 0, 0.25, 0.47, 0.83, 1.8 and 3.7 µg/l) from 4 hours of fertilization for 88 days. At the time the study was performed, the higher water solubility of the alpha and beta isomers was not recognized. Further, the commercial product consisted of >80% of the gamma diasteromer. The LC50, NOEC and LOEC were > the highest dose tested, which were based on the gamma diasteromer. Correcting for gamma diasteromer content, the NOEC was > 8.5 µg/L. Under the conditions of the test, HBCDD was not chronically toxic to rainbow trout over the 88 day exposure.
HBCDD's 28 day NOEC following intraperitoneal injection to rainbow trout was 50 mg/kg bw (Ronisz et al., 2004). The NOEC 78 day in European flounder was 800 µg/g TOC(sediment) plus 3000 µg/g lipid (food) or 8000 µg/g TOC (sediment) and 0 µg/g lipid (food).
Muscle levels corresponding to these NOEC values were up to 446 ug HBCD/g lipid weight (Kuiper et al, 2007). The dose of 8000 µg/g TOC sediment converts to 18.8 mg HBCDD/kg sediment wet weight, based on information provided in the publication. Thus, HBCDD was not chronically toxic to rainbow trout or flounder when administered at doses higher than those used in the fish early life stage test.
NOTE1: the 8000 µg/g TOC sediment was converted to mg/L to derive the NOEC in marine fish for the CSA value above.
NOTE2: the highest food dose, 3000 µg/g lipid, converts to approximately 1.3 µg/g fish bw for the first three wwwks of the test and to 2.6 µg/g fish bw for the rest of the test based on food lipid content and initial fish body weight.
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