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EC number: 217-568-2 | CAS number: 1889-67-4
- 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
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- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
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- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
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- Nanomaterial surface chemistry
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- Endpoint summary
- Stability
- Biodegradation
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- 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
Endpoint summary
Administrative data
Description of key information
Skin:
1,1'-(1,1,2,2-tetramethylethylene)dibenzene resulted in a primary irritation index of 0 (erythema and edema score over 24/48/72 h = 0) when applied to the intact rabbit skin.
Eye:
1,1'-(1,1,2,2-tetramethylethylene)dibenzene resulted in a slight conjunctivae redness which was reversible within at least 72 h (mean score 24/48/72 h: 0.33 - 0.67) when applied to the rabbits eye. No adverse effects were observed for parameters cornea, iris and discharge (score 0 in all animals).
Key value for chemical safety assessment
Skin irritation / corrosion
Link to relevant study records
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- from 1993-02-23 to 1993-02-26
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Version / remarks:
- adopted May 12, 1981
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
- Version / remarks:
- 84/449/EEC
- Deviations:
- no
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Broekman Institute, Someren, The Netherlands
- Age at study initiation: Approx. 12 weeks
- Weight at study initiation: 2410 - 2674 g
- Housing: Individually in labelled cages with perforated floors and equipped with an automatic drinking system.
- Diet: Standard laboratory rabbit diet (LKK-20, peller diameter 4mm, Hope Farms, Woerden, The Netherlands) approx. 100 g per day.
- Water: Free access to tap-water diluted with decalcified water.
- Acclimation period: at least five days before start of treatment under test conditions.
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21
- Humidity (%): 55
- Air changes (per hr): 15
- Photoperiod (hrs dark / hrs light): 12/12 - Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: the untreated contralateral flank served as negative control.
- Amount / concentration applied:
- TEST MATERIAL
- Amount applied: 0.5 g, using a moistened Scotchpak-non-woven patch. - Duration of treatment / exposure:
- 4 h
- Observation period:
- 72 h
- Number of animals:
- 3 male rabbits
- Details on study design:
- TEST SITE
- Area of exposure: dorsal
- coverage: 10 cm x 15 cm were shaved, treatment area 2 x 3 cm.
- Type of wrap if used: elastic bandage (Coban, 3M, St. Paul, USA)
REMOVAL OF TEST SUBSTANCE
- Washing: The remaining test substance was removed using a tissue moistened with tap-water and subsequently dried with a tissue.
- Time after start of exposure: 4 h
SCORING SYSTEM: according to OECD and EU Guidelines (Draize system). - Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritant / corrosive response data:
- No skin irritation was caused by the test substance after a 4 hour dermal application. There was no evidence of a corrosive effect on the skin.
- Other effects:
- No staining of the treated skin by the test substance was observed. No symptoms of systemic toxicity were observed in the animals during the test period and no mortality occurred.
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- 1,1'-(1,1,2,2-tetramethylethylene)dibenzene resulted in a primary irritation index of 0 (erythema and edema score over 24/48/72 h = 0), when applied to the intact rabbit skin.
- Executive summary:
1,1'-(1,1,2,2-tetramethylethylene)dibenzene was applied onto shaved skin of three albino rabbits (New Zealand White) using semi-occlusive dressings for 4 hours, followed by four observations at approximately 1, 24, 48 and 72 hours after removal of the dressings and remaining test substance. The study was performed according to OECD 404 and Regulation (EC) No 440/2008 Method B.4. Under the conditions of this study, no skin irritation was caused by 1,1'-(1,1,2,2-tetramethylethylene)dibenzene and no corrosive effect occurred on the skin in any of the three rabbits. In the area of application, no staining of the treated skin by 1,1'-(1,1,2,2-tetramethylethylene)dibenzene was observed. No signs of intoxication were observed during the study period. 1,1'-(1,1,2,2-tetramethylethylene)dibenzene resulted in a primary irritation index of 0 (erythema and edema score over 24 /48/72 h = 0), when applied to the intact rabbit skin and is thus classified as not irritating to the skin.
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 1983
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- no
- Species:
- rabbit
- Strain:
- New Zealand White
- Type of coverage:
- occlusive
- Preparation of test site:
- other: intact and abraded skin
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount applied: 0.5 g - Duration of treatment / exposure:
- 24 h
- Observation period:
- 72 h
- Number of animals:
- 6 animals (intact skin)
6 animals (abraded skin)
No information on sex. - Details on study design:
- TEST SITE
- Area of exposure: 1 inch x 1 inch
- Type of wrap if used: The patches are fixed to the application site by means of adhesive tape and the entire trunk of the rabbits is wrapped with an impervious material to maintain the test patches in position and to retard evaporation of volatile substances.
REMOVAL OF TEST SUBSTANCE
- Washing: yes
- Time after start of exposure: 24 h
SCORING SYSTEM: according to Draize - Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- (6 animals)
- Time point:
- other: 24/72 h
- Score:
- 0.167
- Max. score:
- 4
- Remarks on result:
- other: intact skin
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- (6 animals)
- Time point:
- other: 24/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: intact skin
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- (6 animals)
- Time point:
- other: 24/72 h
- Score:
- 0.083
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 h
- Remarks on result:
- other: abraded skin
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- (6 animals)
- Time point:
- other: 24/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: abraded skin
- Irritant / corrosive response data:
- After 4 hours two out of twelve rabbits showed very slight erythema. After 52 hours one out of twelve rabbits showed very slight erythema of the treated skin.
- Other effects:
- none
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- 1,1'-(1,1,2,2-tetramethylethylene)dibenzene is not irritating when applied to intact and abraded rabbit skin.
- Executive summary:
In a primary dermal irritation study, New Zealand White rabbits (6 aminals) were dermally exposed to 0.5 g of 1,1'-(1,1,2,2-tetramethylethylene)dibenzene for 24 hours to the intact and abraded skin. Animals then were observed for 3 days. Irritation was scored by the method of Draize. Mean erythema scores of 0.167 and 0.083 (24/72 h) and mean edema scores of 0 (24/72 h) were noted. Thus, in this study, 1,1'-(1,1,2,2-tetramethylethylene)dibenzene is not a dermal irritant.
- Endpoint:
- skin corrosion: in vitro / ex vivo
- Data waiving:
- study scientifically not necessary / other information available
- Justification for data waiving:
- an in vitro skin irritation study does not need to be conducted because adequate data from an in vivo skin irritation study are available
Referenceopen allclose all
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Link to relevant study records
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- from 1993-02-24 to 1993-02-27
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Version / remarks:
- adopted February 24, 1987
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
- Version / remarks:
- 84/449/EEC
- Deviations:
- no
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Broekman Institute, Someren, The Netherlands
- Age at study initiation: Approx. 12 weeks
- Weight at study initiation: 2689 - 2993 g
- Housing: Individually in labelled cages with perforated floors and equipped with an automatic drinking system.
- Diet: Standard laboratory rabbit diet (LKK-20, peller diameter 4mm, Hope Farms, Woerden, The Netherlands) approx. 100 g per day.
- Water: Free access to tap-water diluted with decalcified water.
- Acclimation period: at least five days before start of treatment under test conditions.
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21
- Humidity (%): 55
- Air changes (per hr): 15
- Photoperiod (hrs dark / hrs light): 12/12 - Vehicle:
- unchanged (no vehicle)
- Controls:
- other: the untreated eye served as reference control
- Amount / concentration applied:
- TEST MATERIAL
- Amount applied: 64 ± 1 mg per animal - Duration of treatment / exposure:
- single treatment for 24 h
- Observation period (in vivo):
- 72 h
- Number of animals or in vitro replicates:
- 3 male rabbits
- Details on study design:
- SCORING SYSTEM: according to EU and OECD guidelines (Draize system)
TOOL USED TO ASSESS SCORE: fluorescein, pocket flash light - Irritation parameter:
- cornea opacity score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Irritation parameter:
- iris score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Irritation parameter:
- iris score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.67
- Max. score:
- 3
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.67
- Max. score:
- 3
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 3
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0.56
- Max. score:
- 3
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- chemosis score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritant / corrosive response data:
- Instillation of the test substance into one eye of each of the three male albino rabbits affected the conjunctivae. The irritation of the conjunctivae had resolved within 48 h in one animal and within 72 h after instillation in the two other animals. Treatment of the eyes with 2% fluorescein, 24 h after test substance instillation revealed no corneal epithelial damage in any of the animals.
There was no evidence of ocular corrosion. - Other effects:
- No staining of per-ocular tissues by the test substance was observed. No toxic symptoms were observed in the animals during the test period and no mortality occurred.
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- 1,1'-(1,1,2,2-tetramethylethylene)dibenzene resulted in a slight conjunctivae redness which was reversible within at least 72 h (mean score 24/48/72 h: 0.33 - 0.67), when applied to the rabbits eye. No adverse effects were observed for parameters cornea, iris and discharge (score 0 in all animals).
- Executive summary:
The eye irritation potential of 1,1'-(1,1,2,2-tetramethylethylene)dibenzene was assessed according to OECD guideline 405 and EU method B.5. The test item was instilled into one eye of each of three male albino rabbits (New Zealand White), followed by four observations at approximately 1, 24, 48 and 72 h after test substance administration. Under the conditions of the study, 1,1'-(1,1,2,2-tetramethylethylene)dibenzene resulted in adverse effects on the conjunctivae in all three animals, which had resolved within 48 - 72 h after instillation (mean score 24/48/72 h: 0.33 - 0.67). Ocular corrosion was not observed in any of the rabbits. No signs of systemic intoxication were observed during the study period. In conclusion, 1,1'-(1,1,2,2-tetramethylethylene)dibenzene was considered as not irritating to the eye.
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 1983
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- not specified
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
- Deviations:
- not specified
- GLP compliance:
- no
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- The animals were caged individually and received no hay or other extraneous material that might enter the eyes.
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: the untreated eye served as control
- Amount / concentration applied:
- TEST MATERIAL
- Amount applied: 100 mg - Duration of treatment / exposure:
- single treatment
- Observation period (in vivo):
- 72 h
- Number of animals or in vitro replicates:
- 6 animals (sex not specified).
- Details on study design:
- SCORING SYSTEM: according to Draize
TOOL USED TO ASSESS SCORE: Ocular reactions were read using a binocular magnifying glass. - Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Remarks:
- (6 animals)
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- iris score
- Basis:
- mean
- Remarks:
- (6 animals)
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Remarks:
- (6 animals)
- Time point:
- 24/48/72 h
- Score:
- 0.78
- Max. score:
- 3
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Remarks:
- (6 animals)
- Time point:
- 24/48/72 h
- Score:
- 0.56
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 h
- Irritant / corrosive response data:
- After 24 hours the eye effects caused by the test material consisted of slight to moderate redness and slight swelling of the conjunctivae. After 72 hours these eye effects had cleared up completely.
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- 1,1'-(1,1,2,2-tetramethylethylene)dibenzene resulted in a slight to moderate irritation which was reversible within at least 72 h (mean score 24/48/72 h: conjunctivae = 0.78, chemosis = 0.56) when applied to the rabbits eye. No adverse effects were observed for parameters cornea and iris (score 0 in all 6 animals).
- Executive summary:
In a primary eye irritation study, 100 mg 1,1'-(1,1,2,2-tetramethylethylene)dibenzene were instilled into the conjunctival sac of 6 New Zealand White rabbits. Animals then were observed for 3 days. Irritation was scored by the method of Draize.
1,1'-(1,1,2,2-tetramethylethylene)dibenzene resulted in a slight to moderate irritation which was reversible within at least 72 h (mean score 24/48/72 h: conjunctivae = 0.78, chemosis = 0.56) when applied to the rabbits eye. No adverse effects were observed for parameters cornea and iris (score 0 in all 6 animals). Thus, in this study, 1,1'-(1,1,2,2-tetramethylethylene)dibenzene is not an eye irritant.
- Endpoint:
- eye irritation: in vitro / ex vivo
- Data waiving:
- study scientifically not necessary / other information available
- Justification for data waiving:
- an in vitro eye irritation study does not need to be conducted because adequate data from an in vivo eye irritation study are available
Referenceopen allclose all
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Skin:
- Key study
1,1'-(1,1,2,2-tetramethylethylene)dibenzene was applied onto shaved skin of three albino rabbits (New Zealand White) using semi-occlusive dressings for 4 hours, followed by four observations at approximately 1, 24, 48 and 72 hours after removal of the dressings and remaining test substance. The study was performed according to OECD 404 and Regulation (EC) No 440/2008 Method B.4. Under the conditions of this study, no skin irritation was caused by 1,1'-(1,1,2,2-tetramethylethylene)dibenzene and no corrosive effect occurred on the skin in any of the three rabbits. In the area of application, no staining of the treated skin by 1,1'-(1,1,2,2-tetramethylethylene)dibenzene was observed. No signs of intoxication were observed during the study period. 1,1'-(1,1,2,2-tetramethylethylene)dibenzene resulted in a primary irritation index of 0 (erythema and edema score over 24 /48/72 h = 0), when applied to the intact rabbit skin and is thus classified as not irritating to the skin.
- Supporting study
In a primary dermal irritation study, New Zealand White rabbits (6 aminals) were dermally exposed to 0.5 g of 1,1'-(1,1,2,2-tetramethylethylene)dibenzene for 24 hours to the intact and abraded skin. Animals then were observed for 3 days. Irritation was scored by the method of Draize. Mean erythema scores of 0.167 and 0.083 (24/72 h) and mean edema scores of 0 (24/72 h) were noted. Thus, in this study, 1,1'-(1,1,2,2-tetramethylethylene)dibenzene is not a dermal irritant.
Eye:
- Key study
The eye irritation potential of 1,1'-(1,1,2,2-tetramethylethylene)dibenzene was assessed according to OECD guideline 405 and EU method B.5. The test item was instilled into one eye of each of three male albino rabbits (New Zealand White), followed by four observations at approximately 1, 24, 48 and 72 h after test substance administration. Under the conditions of the study, 1,1'-(1,1,2,2-tetramethylethylene)dibenzene resulted in adverse effects on the conjunctivae in all three animals, which had resolved within 48 - 72 h after instillation (mean score 24/48/72 h: 0.33 - 0.67). Ocular corrosion was not observed in any of the rabbits. No signs of systemic intoxication were observed during the study period. In conclusion, 1,1'-(1,1,2,2-tetramethylethylene)dibenzene was considered as not irritating to the eye.
- Supporting study
In a primary eye irritation study, 100 mg 1,1'-(1,1,2,2-tetramethylethylene)dibenzene were instilled into the conjunctival sac of 6 New Zealand White rabbits. Animals then were observed for 3 days. Irritation was scored by the method of Draize.
1,1'-(1,1,2,2-tetramethylethylene)dibenzene resulted in a slight to moderate irritation which was reversible within at least 72 h (mean score 24/48/72 h: conjunctivae = 0.78, chemosis = 0.56) when applied to the rabbits eye. No adverse effects were observed for parameters cornea and iris (score 0 in all 6 animals). Thus, in this study, 1,1'-(1,1,2,2-tetramethylethylene)dibenzene is not an eye irritant.
Justification for classification or non-classification
Classification, Labelling, and Packaging Regulation (EC) No. 1272/2008
The available experimental test data are reliable and suitable for classification purposes under Regulation (EC) No. 1272/2008. As a result the substance is not considered to be classified for skin corrosion/irritation and eye damage/irritation under Regulation (EC) No. 1272/2008, as amended for the eighteenth time in Regulation (EU) 2022/692.
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