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EC number: 208-792-1 | CAS number: 541-73-1
- 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

Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Comparable to guideline study with acceptable deviations
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 980
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- Analytical purity not reported. Draize score. Observational period was too short. Eyes were not rinsed after exposure
- GLP compliance:
- no
- Remarks:
- GLP was not mandatory at the time of the study
Test material
- Reference substance name:
- 1,3-dichlorobenzene
- EC Number:
- 208-792-1
- EC Name:
- 1,3-dichlorobenzene
- Cas Number:
- 541-73-1
- Molecular formula:
- C6H4Cl2
- IUPAC Name:
- 1,3-dichlorobenzene
- Details on test material:
- - Name of test material (as cited in study report): m-dichlorobenzene
- Analytical purity: no data
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: W. Ostrop, Meerbusch, Germany
- Weight at study initiation: 3.1 Kg
- Housing: the animals were individually housed
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 7-14 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 16-18°C
- Humidity (%): 40%
- Photoperiod (hrs dark / hrs light): 12 hrs dark / 12 hrs light
Test system
- Vehicle:
- not specified
- Controls:
- other: the left eye served as control
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 100 µL - Duration of treatment / exposure:
- 8 days
- Observation period (in vivo):
- 24, 48, 72 hours and 8 days
- Number of animals or in vitro replicates:
- 6
- Details on study design:
- SCORING SYSTEM: Draize score
TOOL USED TO ASSESS SCORE: fluorescein
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Remarks:
- of 6 animals
- Time point:
- 24/48/72 h
- Score:
- 0.3
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 days
- Irritation parameter:
- iris score
- Basis:
- mean
- Remarks:
- pf 6 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Reversibility:
- other: not applicable
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Remarks:
- of 6 animals
- Time point:
- 24/48/72 h
- Score:
- 0.55
- Max. score:
- 3
- Reversibility:
- other: During the observation period of 8 days, 1/6 animal presented, diffuse, carmine redness. Individual vessels were not easily distinguishable.
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Remarks:
- of 6 animals
- Time point:
- 24/48/72 h
- Score:
- 0.4
- Max. score:
- 4
- Reversibility:
- other: During the observation period of 8 days, 1/6 animal presented slight swelling (any swelling) above normal, and 1/6 one animal presented distinct swelling with partial detachment of the eyelid
- Irritation parameter:
- other: discharge
- Basis:
- mean
- Remarks:
- of 6 animals
- Time point:
- other: 24, 48, 72 hours
- Score:
- 0.35
- Max. score:
- 3
- Reversibility:
- fully reversible within: 8 days
- Irritant / corrosive response data:
- see Remarks on results including tables and figures
Any other information on results incl. tables
Readings |
Animal |
Cornea |
Iris |
Conjunctiva Redness |
Conjunctiva Chemosis |
Discharge |
24h |
1 |
0 |
0 |
0 |
0 |
0 |
24h |
2 |
1 |
0 |
1 |
0 |
0 |
24h |
3 |
0 |
0 |
0 |
0 |
0 |
24h |
4 |
0 |
0 |
0 |
0 |
0 |
24h |
5 |
0 |
0 |
1 |
1 |
0 |
24h |
6 |
1 |
0 |
1 |
1 |
1 |
48h |
1 |
0 |
0 |
0 |
0 |
0 |
48h |
2 |
1 |
0 |
1 |
0 |
0 |
48h |
3 |
0 |
0 |
0 |
0 |
0 |
48h |
4 |
0 |
0 |
0 |
0 |
0 |
48h |
5 |
0 |
0 |
2 |
1 |
0 |
48h |
6 |
1 |
0 |
1 |
1 |
0 |
72h |
1 |
0 |
0 |
0 |
0 |
0 |
72h |
2 |
0 |
0 |
2 |
1 |
0 |
72h |
3 |
0 |
0 |
0 |
0 |
0 |
72h |
4 |
0 |
0 |
0 |
0 |
0 |
72h |
5 |
0 |
0 |
0 |
0 |
0 |
72h |
6 |
1 |
0 |
2 |
2 |
3 |
Mean24-72h
|
1 |
0 |
0 |
0 |
0 |
0 |
Mean24-72h
|
2 |
0.7 |
0 |
1.3 |
0.3 |
0 |
Mean 24-72h
|
3 |
0 |
0 |
0 |
0 |
0 |
Mean 24-72h
|
4 |
0 |
0 |
0 |
0 |
0 |
Mean 24-72h
|
5 |
0 |
0 |
1 |
0.7 |
0 |
Mean 24-72h
|
6 |
1 |
0 |
1.3 |
1.3 |
1.3 |
Total Mean |
|
0.3 |
0 |
0.55 |
0.4 |
0.35 |
e (hrs) |
Individual scoring |
||||||
Animal 1 |
Animal 2 |
Animal 3 |
Animal 4 |
Animal 5 |
Animal 6 |
||
Corneal opacity |
|||||||
8 days |
0 |
0 |
0 |
0 |
0 |
0 |
|
Iritis |
|||||||
8 days |
0 |
0 |
0 |
0 |
0 |
0 |
|
Redness |
|||||||
8 days |
0 |
2 |
0 |
0 |
0 |
0 |
|
Chemosis |
|||||||
8 days |
0 |
1 |
0 |
0 |
0 |
2 |
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Under the conditions of this study, the test item is not irritating to the eye according to CLP Regulation (EC) No 1272/2008.
- Executive summary:
The eye irritation/corrotion effects of 1,3-dichlorobenzene were tested with a test similar to OECD guideline 405 with acceptable restrictions (Analytical purity not reported. Draize score. Observational period was too short. Eyes were not rinsed after exposure).
The test substance was applied into the conjunctival sac (right lower eyelids) of 6 rabbits. The evaluation was made using an ophthalmoscope.
The corneal findings were 8 days after the treatment confirmed with the fluorescein testAccording to the findings of this test 1,3-dichlorobenzene can be considered as not irritating to eyes. The skin irritation/corrosion potential of the test substance was assesed in line with an OECD TG 405 study where under the conditions of this study, the test substance was determined to be irritating to the skin and a Category 2 skin irritant according to CLP Regulation (EC) No. 1272/2008. Therefore the substance was classified according to the CLP Regulation (EC) No. 1272/2008.
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