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EC number: 244-617-5 | CAS number: 21850-44-2
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1997
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP study conducted using OECD guidelines
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 997
- Report date:
- 1997
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- TBBA-bis(2,3-dibromopropyl ether)
- IUPAC Name:
- TBBA-bis(2,3-dibromopropyl ether)
- Reference substance name:
- 1,1'-(isopropylidene)bis[3,5-dibromo-4-(2,3-dibromopropoxy)benzene]
- EC Number:
- 244-617-5
- EC Name:
- 1,1'-(isopropylidene)bis[3,5-dibromo-4-(2,3-dibromopropoxy)benzene]
- Cas Number:
- 21850-44-2
- Molecular formula:
- C21H20Br8O2
- IUPAC Name:
- 1,1'-propane-2,2-diylbis[3,5-dibromo-4-(2,3-dibromopropoxy)benzene]
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- Sponsors identification: SR-720
Data received: 15 January 1997
Description: White powder
Storage conditions: ambient temperature (< 25°C) stored under artifical light
Constituent 1
Constituent 2
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- Three rabbits were supplied by David Percival Ltd, Moston, Sandbach, Cheshire UK.
Weight at the start of the experiment: 2.67-3.02 kg; 12-16 weeks old.
After minimum acclimatisation of 5 days each animal was given a number.
The animals were housed individually in suspended metal cages, with free access to drinking water and food.
The animal room was maintained at a temperature of 17-19°C and relative humidity of 45-50%.
The air exchange was approx. 15 changes per hr and the lighting was controlled by a time switch to give 12 hr continous light and 12 hr darkness.
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- clipped
- Vehicle:
- water
- Controls:
- not specified
- Amount / concentration applied:
- 0.5 gr of test material moistened with 0.5 ml of distilled water was applied
- Duration of treatment / exposure:
- 4 hr
- Observation period:
- The sites were examined approx. 1, 24, 48 and 72 hr following the removal of the patches.
- Number of animals:
- 3
- Details on study design:
- On the day before the test each rabbit was clipped free of fur from the dorsal flank area using vetrinary clippers.
On the day of the test a suitable test site was selected on the back of each rabbit. A quantity of 0.5g of test material moistened with o.5 ml of distilled water, was introduced under 2.5 cm x 2.5 cm cotton gauze patch and placed in position on the shorn skin.
the patch was secured in position with a surgical adhesive tape. To prevent the animals interfering with the patches, the trunk of each rabitt was wrapped in an elastic corset, and the animals were returned to their cages for the duration of the exposed period.
Four hr after application the corset and patches were removed from each animal and any residual test material removed by gentle swabbing with cotton wool and soaked in distilled water.
Approx. 1 hr following the removal of the patches and 24, 48 and 72 hr later the test sites were examined for evidance of primary irritation and scored according to the scale from Draze JH (1977).
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- animal #1
- Time point:
- other: 1, 24, 48 and 72 hr
- Score:
- 0
- Remarks on result:
- other: Erythema/Eschar formation/Oedema formation
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- animal #2
- Time point:
- other: 1, 24, 48 and 72 hr
- Score:
- 0
- Remarks on result:
- other: Erythema/Eschar formation/Oedema formation
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- animal #3
- Time point:
- other: 1, 24, 48 and 72 hr
- Score:
- 0
- Remarks on result:
- other: Erythema/Eschar formation/Oedema formation
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The test material produced a primary irritation index of 0.0 and was classified as NON-IRRITANT to rabbit skin according to the Draize classification scheme. No corrosive effects were noted.
- Executive summary:
Acute dermal irritation study was conducted on New Zealand White rabbits under OECD guideline 404 and EU method B4. A single 4 hr, semi-occluded application of the test material to the intact skin of 3 rabbits produced no evidence of skin irritation. The test material produced a primary irritation index of 0.0 and was classified as NON-IRRITANT to rabbit skin according to the Draize classification scheme. No corrosive effects were noted.
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