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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 700-158-7 | CAS number: 1092834-40-6
- 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
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 27 April - 22 May 2009
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Guideline study but the test substance is highly insoluble in water and analytical verification of test concentrations difficult.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 009
- Report date:
- 2009
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- The Department of Health of the Government of the United Kingdom
Test material
Reference
- Name:
- Unnamed
- Type:
- Constituent
- Details on test material:
- - Name of test material (as cited in study report): Benzene, 1,1 ‘-(1‚2-ethanediyl)bis-, brominated, [CAS No. 1092834-40-6]; product name: SH-1; reaction product of bromine and 1,2-diphenylethane
- Substance type: white powder
- Physical state: solid
- Analytical purity: >99%
- Composition of test material, percentage of components: Penta bromodiphenylethane 0-2%, Hexa bromodiphenylethane 40-80%, Hepta bromodiphenylethane 1-20%, Octa bromodiphenylethane 1-30%, Nona bromodiphenylethane 0-10%, Deca bromodiphenylethane 0-5%
- Lot/batch No.: 20090105
- Expiration date of the lot/batch: 08 January 2011
- Storage condition of test material: room temperature in the dark
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- The concentration and stability of the test material in the test preparations were verifled by chemical analysis at 0 and 48 hours.
Test solutions
- Vehicle:
- no
- Details on test solutions:
- The test material was insoluble in water. Pre-study solubility work conducted indicated that it was not possible to obtain a testable solution of the test material using traditional methods of preparation e.g. ultrasonicatiori and high shear mixing. A pre-study media preparation trial indicated that a dissolved test material concentration of approximately 0.0041 mg/l was obtained from a saturated solution method of preparation indicating this to be the limit of water solubility of this material under test conditions.
An amount of test material (550 mg) was dispersed, in duplicate, in 11 litres of reconstituted water with the aid of propeller stirring at approximately 1500 rpm at a temperature of approximately 20°C for 24 hours. After 24 hours the stirring was stopped and any undissolved test material was removed by centrifugation at 10000 g for 30 minutes to give a saturated solution with a 0-Hour measured test concentration of 0.0016 mg/l.
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: water flea
- Strain: 1st instar
- Source: derived from in-house laboratory cultures
- Age at study initiation (mean and range, SD): < 24h
- Method of breeding: at 20°C, 16 hours light , 8 hours dark
- Feeding during test
- Food type: suspension of Chlorella
- Frequency: daily
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
Test conditions
- Test temperature:
- 20°C ± 1°C; The temperature throughout the test was observed to be slightly in excess of the 20°C ± 1°C range given in the Protocol. This deviation was considered not to have any impact on the outcome or validity of the test as no adverse effects of exposure were observed throughout the test.
- Nominal and measured concentrations:
- The test concentration of 0.0016 mg/I was the highest attainable test concentration that could be prepared due to the Iimited solubility of the test material in water.
Analysis of the test preparations at 0 hours showed measured test concentrations to range from 0.001 61 mg/l to 0.00167 mg/l.
Analysis of the old or expired test preparations at 48 hours showed a slight decline in measured test concentrations of 0.000514 mg/l to 0.00106 mg/l.
lt was therefore considered justifiable to base the results on the geometric mean measured test concentrations in order to give a “worst case“ analysis of the data. The use of geometric mean measured test concentrations was considered not to have affected the results of the test. - Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Type (delete if not applicable): closed
- Material, size, headspace, fill volume: 250 mL glass jars containing approx. 250 mL test preparation
- Aeration: no
- Renewal rate of test solution (frequency/flow rate): not renewed
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
OTHER TEST CONDITIONS
- Photoperiod: 16 hours light, 8 hours dark with 20 min dawn and dusk transition periods
TEST CONCENTRATIONS
- Range finding study: 0.000041, 0.00041 and 0.0041 mg/L. Test material prepared from a saturated solution. - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.001 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- dissolved
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- > 0.001 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- dissolved
- Basis for effect:
- mobility
- Results with reference substance (positive control):
- Daphnia magna was exposed to an aqueous solution of the reference material at conceritrations of 0.32, 0.56, 1.0, 1.8 and 3.2 mg/l for 48 hours at a temperature of approximately 20°C under static test conditions. Immobilisation and any adverse reactions to exposure were recorded after 3, 24 and 48 hours.
The 48-Hour EC50 for the reference material to Daphnia magna based on nominal concentrations was 0.71 mg/l with 95% confidence limits of 0.61 — 0.81 mg/l. The No Observed Effeet Concentration was 0.32 mg/l.
Any other information on results incl. tables
The acute toxicity of the test material to the freshwater invertebrate Daphnia magna has been investigated and based on the 0-hour measured test concentration gave a 48-hour EC50 of greater than 0.0016 mg/L. Correspondingly the No Observed Effect Concentration was 0.0016 mg/L.
The 48 -hour EC50 based on the geometric mean measured test concentrations was greater than 0.0011 mg/L and correspondingly the NO Observed Effect Concentration was 0.0011 mg/L.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- The acute toxicity of the test material to the freshwater invertebrate Daphnia magna has been investigated and based on the 0-Hour measured test concentration gave a 48-Hour EC50 of greater than 0.0016 mg/l. Correspondingly the No Observed Effect Concentration was 0.0016 mg/l.
The 48-Hour EC50 based on the geometric mean measured test concentrations was greater than 0.0011 mg/l and correspondingly the No Observed Effect Concentration was 0.0011 mg/l.
This study showed that there were no toxic effects at saturation.
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.