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EC number: 284-366-9 | CAS number: 84852-53-9
- 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
Water solubility
Administrative data
- Endpoint:
- water solubility
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Sept 17, 1999 to Nov 17, 1999
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Referenceopen allclose all
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 999
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 2 007
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 830.7860 (Water Solubility Generator Column Method)
- Deviations:
- no
- GLP compliance:
- yes
- Type of method:
- column elution method
Test material
- Reference substance name:
- 1,1'-(ethane-1,2-diyl)bis[pentabromobenzene]
- EC Number:
- 284-366-9
- EC Name:
- 1,1'-(ethane-1,2-diyl)bis[pentabromobenzene]
- Cas Number:
- 84852-53-9
- Molecular formula:
- C14H4Br10
- IUPAC Name:
- 1,2,3,4,5-pentabromo-6-[2-(2,3,4,5,6-pentabromophenyl)ethyl]benzene
- Details on test material:
- Test material was the commercial SAYTEX 8010 Flame Retardant product with a purity of 98.93% DBDPEthane.
Constituent 1
- Specific details on test material used for the study:
- The test substance, a white powder, was identified as SAYTEX 8010; Lot # 23827-1K. The test substance had an assigned purity of 98.93% and an expiration date of March 2001.
Results and discussion
Water solubility
- Key result
- Water solubility:
- ca. 0.72 µg/L
- Conc. based on:
- test mat. (dissolved fraction)
- Loading of aqueous phase:
- 0.5 other: g
- Incubation duration:
- 30 min
- Temp.:
- 25 °C
- pH:
- 0
- Remarks on result:
- other:
- Remarks:
- pH was not measured
- Details on results:
- The limit of detection (LOD) was determined to be 0.610 ug/L, calculated as the mean plus three times the standard deviation of background response of four matrix blank sample injections. The limit of quantitation (LOQ) was dtermined to be 0.896 ug/L calculated as the mean plus ten times the standard deviation of background response of four matrix blank injections. The temperature of the water bath remained constant at 25.0 +/- 0.05 degress C throughout the experiment.
Any other information on results incl. tables
The nominal flow rate of reagent water throught the generator column was measured prior to the start of sample collection for each flow rate and was found to be accurate for purposes of this study. The pump setting of 1.0 -ml/min yielded approximately 5.0 mL of eluant in a 5 minjute period of collection into a 10 mL graduated cylinder. The pump setting of 0.5 mL/min yielded approximately 2.5 mL of eulant in a 5 min period of collection into a 10 mL graduated cylinder. No interferences were observed at or above the LOQ in any of the injections of the matrix blank. The % recovery of the extraction efficiency samples fortified at 1.00, 5.00 and 10.0 ug SAYTEX 8010/L and extracted along with the generator column fractions, ranged from 82.1 to 92.4% of nominal. The saturated concentration of SAYTEX 8010 in the eluate samples collected from the generator column (0.635 ug/L) at a flow rate of 1.0 mL/min was between the LOQ and LOD. The saturated concentration at a flow rate of 0.5 mL/min was 0.795 ug/L. The overall solubility, calculated as the mean of estimated solubilites determined at the two flow rates, was estimated to be approximately 0.72 ug/L.
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information): insoluble (< 0.1 mg/L)
The overall solubility, calculated as the mean of estimated solubilites determined at the two flow rates, was approximately 0.72 ug/L and was between the LOD and LOQ. Thus, the substance is considered insoluble. - Executive summary:
The overall solubility, calculated as the mean of estimated solubilites determined at the two flow rates, was approximately 0.72 ug/L, and was between the LOD and LOQ. Thus, the substance is considered insoluble (<0.1 mg/L).
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