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EC number: 603-094-7 | CAS number: 125904-11-2
- 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
Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 6 to 8 November 1980
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study conducted in accordance with generally accepted scientific principles, possibly with incomplete reporting or methodological deficiencies, which do not affect the quality of the relevant results.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 980
- Report date:
- 1980
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: Regulations of MTB, Code of Federal Regulations, Vol. 49, Part 173.343(2), 1976
- Deviations:
- not specified
- Principles of method if other than guideline:
- Two groups of 5 male Sprague-Dawley rats were exposed, whole body, to the material via inhalation at different but consecutive times. Target concentration was 2 mg/L. Nominal concetrations were 3.1 mg/L and 2.8 mg/L for the first and second group, respectively. The test material was nebulized into a a 37.5 L glass exposure chamber with a DeVilbsis continuous flow nebulizer. The test material was stored in refrigerator until the hour of exposure. The nebulization rate was maintained at 11.7 mg/min, while the air exchange rate within the chanber was maintained at 3.8 L/min for the first group. The nebulization rate was maintained at 10.0 mg/min, while the air exchange rate within the chanber was maintained at 3.6 L/min for the second group. Animals were observed during the 1 hour exposure and for 2 days thereafter. Body weights were recorded just prior to exposure and again on test days 2 and 3. No necropsy was performed.
- GLP compliance:
- no
- Remarks:
- but QA statement included in the report
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Benzene, dibromoethyl Benzene, ethenyl-, ar-bromo derivs.
- EC Number:
- 603-094-7
- Cas Number:
- 125904-11-2
- Molecular formula:
- C8 H6 Br2
- IUPAC Name:
- Benzene, dibromoethyl Benzene, ethenyl-, ar-bromo derivs.
- Test material form:
- liquid
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Harlan Industries, Inc., Madison, Wisconsin
- Age at study initiation: 8 weeks
- Weight at study initiation: 292 to 319 g
- Housing: individually
- Diet (e.g. ad libitum): Purina Rat Chow ad libitum except during the 1 hour exposure
- Water (e.g. ad libitum): ad libitum except during the 1 hour exposure
- Acclimation period: at least 7 days
ENVIRONMENTAL CONDITIONS
Temperature controlled quarters (no more details available)
IN-LIFE DATES: From: 6 To: 8 November 1980
Administration / exposure
- Route of administration:
- inhalation
- Type of inhalation exposure:
- whole body
- Vehicle:
- not specified
- Details on inhalation exposure:
- Exposures were conducted in a 37.5 L glass exposure chanber. Air flow through the chamber was provided with a wet test meter, and vacum pump. An air tube containing a desiccate was connected into the line of the air flow system between the exhaust port of the chamber and the wet test meter. This collected or filtered out the test material which was contained within the atmosphere that was exhausted from the chamber. The test material was administered into the chamber near the junction of the air inlet port, which usually allows the test material and incoming air to mix evenly within the chamber at the top before being drawn down and around the animals.
- Analytical verification of test atmosphere concentrations:
- no
- Duration of exposure:
- 1 h
- Concentrations:
- Target 2 mg/L. Nominal 3.1 and 2.8 mg/L.
- No. of animals per sex per dose:
- 5 males per group
- Control animals:
- no
- Details on study design:
- Animals were examined during the 1 hour exposure and for 2 days therefater. Body weight was recorded prior to exposure and on days 2 and 3. No necropsy was performed.
- Statistics:
- None
Results and discussion
Effect levels
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- > 2 mg/L air (nominal)
- Exp. duration:
- 1 h
- Remarks on result:
- other: target concentration
- Mortality:
- No mortality occurred.
- Clinical signs:
- other: Reactions during exposure included lacrimation, clear nasal discharge, inactivity, and rapid, shallow breathing. All animals appeared normal in the afternoon following exposure and during the 2-day observation period.
- Body weight:
- Mean body weights showed an increase in both groups during the 3 days of test. Individual values showed minimal body weight losses in 3 rats of the first group on day 2, followed by body weight gains on day 3.
- Gross pathology:
- Not applicable
Applicant's summary and conclusion
- Interpretation of results:
- other: not a Class "B" poison
- Remarks:
- Criteria used for interpretation of results: other: Regulations of MTB, Code of Federal regulations, Vol. 49, Part 173.343(2), 1976
- Conclusions:
- The acute inhalation LC50 (1 hour) of dibromostyrene was higher than 2 mg/L (target concentration).
- Executive summary:
In an acute inhalation study, two groups of 5 male rats were exposed whole-body to a target concentration of 2 mg/L. Nominal concetrations were 3.1 and 2.8 mg/L, respectively, for the first and second group. Animals were observed during exposure and for 2 days thereafter. Body weight was recoded prior to exposure and on days 2 and 3. No necropsy was performed.
No mortality occurred. Reactions during exposure included lacrimation, clear nasal discharge, inactivity, and rapid, shallow breathing. All animals appeared normal in the afternoon following exposure and during the two days after exposure. Mean body weight increased duirng the 3 days of test.
The LC50 (1 hour) of dibromostyrene was greater than 2 mg/L (target concentration).
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