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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

Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- February 17th, 2009 - February 27th, 2009
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 009
- Report date:
- 2009
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- minor deviation: only 2 instead of 3 animals tested, which was not found to be critical, as the test results were clearly negative
- 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): SH-1
- Chemical name of test material (as cited in study report): Benzene, 1,1'-(1,2-ethanediyl)bis-, brominated
- Composition of test material, percentage of components:
-- 0-2 % Penta bromodiphenylethane (CAS No.: 137563-31-6)
-- 40-80 % Hexa bromodiphenylethane (CAS No.: 137563-32-7)
-- 1-20 % Hepta bromodiphenylethane (CAS No.: 137563-33-8)
-- 1-30 % Octa bromodiphenylethane (CAS No.: 137563-34-9)
-- 0-10 % Nona bromodiphenylethane (CAS No.: 137563-35-0)
-- 0-5 % Deca bromodiphenylethane (CAS No.: 137563-36-1, 84852-53-9)
- Physical state: white powder
- Analytical purity: > 99%
- Batch No.: 20090105
- Expiration date of the lot/batch: January 08th, 2011
- Storage condition of test material: room temperature in the dark
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Harlan Laboratories UK Limited, Bicester, Oxon, UK
- Age at study initiation: 12 - 20 weeks
- Weight at study initiation: 2.69 and 2.89 kg
- Housing: individually in suspended cages
- Diet (e.g. ad libitum): mains drinking water
- Water (e.g. ad libitum): diet supplied by Harlan Teklad, Blackthorn, Bicester, Oxon, UK
- Acclimation period: at least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 17-23
- Humidity (%): 30-70
- Air changes (per hr): at least 15
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: From: February 10th, 2009 To: February 10th, 2009
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- other: clipped using veterinary clippers
- Vehicle:
- water
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 g
VEHICLE
- Amount(s) applied (volume or weight with unit): 0.5 mL distilled water - Duration of treatment / exposure:
- Single application, exposure period:
First rabbit: 3 min, 1 hour, 4 hours (on 3 different sites on the dorsum and dorsal flank area)
Second rabbits: 4 hours - Observation period:
- 72 hours
- Number of animals:
- 2
- Details on study design:
- TEST SITE
- Area of exposure: dorsal flank area (2.5 cm x 2.5 cm)
- Type of wrap if used: cotton gauze patch, surgical adhesive tape, trunk of rabbit wrapped in an elasticated corset for the duration of the exposure period.
REMOVAL OF TEST SUBSTANCE
- Washing (if done): any residual test material was removed by gentle swabbing with cotton wool soaked in distilled water after the exposure time
SCORING SYSTEM: Draize Scheme
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- out of 2 animals
- Time point:
- other: 1, 24, 48, 72 h
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- other: not applicable
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- out of 2 animals
- Time point:
- other: 1, 24, 48, 72 h
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- other: not applicable
Any other information on results incl. tables
3-minute and 1-hour semi occluded applications of the test material to the intact skin of the first rabbit produced no evidence of skin irritation.
A single 4-hour, semi-occluded application of the test material to the intact skin of two rabbits produced no evidence of skin irritation.
All animals showed expected gain in bodyweight during the study.
Table 1: Individual skin examination scores after 4h-exposure to SH-1
(Scoring according to Draize scheme)
Skin effect |
Erythema |
Edema |
||||||||
Scoringa |
1 h |
24 h |
48 h |
72 h |
Meanb |
1 h |
24 h |
48 h |
72 h |
Meanb |
Animal No. /sex |
|
|
|
|
|
|
|
|
|
|
#1 / m |
0 |
0 |
0 |
0 |
0.0 |
0 |
0 |
0 |
0 |
0.0 |
#2 / m |
0 |
0 |
0 |
0 |
0.0 |
0 |
0 |
0 |
0 |
0.0 |
aTimepoint of reading after substance removal subsequent to 4h-dermal exposure
bMean of 24, 48 and 72 h scores
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Not irritating to rabbit skin.
- Executive summary:
In a primary dermal irritation study, the skin irritation/corrosion potential of Benzene, 1,1'-(1,2-ethanediyl)bis-, brominated was tested. The clipped dorso-lateral skin of two male New Zealand White rabbits was exposed to 0.5 mg test material in 0.5 mL distilled water for 4 hours under semi-occlusive conditions. The rabbits were observed for 72 hours. Skin reactions were assessed using the Draize scheme 1, 24, 48 and 72 hours after removal of the test substance.
The exposure period of up to 4 hours produced no evidence of skin irritation at any of the observation intervals.
Based on the study results, the test substance is non-irritating to the skin of rabbits and therefore not classified according to EU classification and OECD GHS classification criteria.
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