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EC number: 230-258-1 | CAS number: 6992-11-6
- 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
Endpoint summary
Administrative data
Description of key information
PB25
The skin irritating potential of the test item was assessed according to OECD TG 404 and GLP conditions. The test item did not reveal any irritation potential on the skin of rabbits.
The eye irritating potential of the test item was assessed according to OECD TG 405 and GLP conditions. No abnormal findings were observed in the treated eye of any animal 7 days after treatment. The test item did not induce significant or irreversible damage to the rabbit eye in this study.
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:
- 2006
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study (OECD TG 404) performed under GLP
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River Deutschland GmbH, Kisslegg, Germany
- Age at study initiation: 11-12 weeks
- Housing: Individually in stainless steel cages equipped with feed hoppers and drinking water bowls.
- Diet: Pelleted standard Provimi Kliba 3418 rabbit maintenance diet (batch no. 85/05; provided by Provimi Kliba AG, CH-4303 Kaiseraugst); ad libitum
- Water: Community tap water from Füllinsdorf, ad libitum
- Acclimation period: 4 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 17-23
- Humidity (%): 30-70
- Air changes (per hr): 10-15
- Photoperiod (hrs dark / hrs light): 12/12 - Type of coverage:
- semiocclusive
- Preparation of test site:
- other: clipped
- Vehicle:
- water
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount applied: 0.5 g/animal moistened with appr. 0.5 mL purified water
VEHICLE
- Amount applied: 0.5 mL/animal - Duration of treatment / exposure:
- 4 h
- Observation period:
- 7 days
- Number of animals:
- 3 (1 male, 2 females)
- Details on study design:
- TEST SITE
- Area of exposure: 4 cm x 4 cm
REMOVAL OF TEST SUBSTANCE
- Washing (if done): flushed with lukewarm tap water
- Time after start of exposure: 4 h
SCORING SYSTEM:
Grading of Skin Reactions according to COMMISSION DIRECTIVE 2004/73/EC, APRIL 29, 2004
ERYTHEMA AND ESCHAR FORMATION
No erythema.......................................................................................................................0
Very slight erythema............................................................................................................1
Well-defined erythema........................................................................................................2
Moderate to severe erythema.............................................................................................3
Severe erythema (beef redness) or eschar formation (injuries in depth preventing erythema) reading.................................................4
OEDEMA FORMATION
No oedema.........................................................................................................................0
Very slight oedema (barely perceptible)..............................................................................1
Slight oedema (edges of area well-defined by definite raising)..........................................2
Moderate oedema (edges raised approximately 1 mm).....................................................3
Severe oedema (raised more than 1 mm and extending beyond the area of exposure)...4 - Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24-48-72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: reversibility not applicable
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24-48-72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: reversibility not applicable
- Irritant / corrosive response data:
- Slight brown staining produced by the colour of the test item on the treated skin was observed in all animals at the 1-hour reading and persisted up to the 48- or 72-hour reading. The test item did not elicit any skin reactions at the application site of any animal at any of the observation times (all scores 0).
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The test item did not reveal any irritation potential on the skin of rabbits, tested in this study according to OECD test guideline no. 404 and GLP conditions.
- Executive summary:
The skin irritating potential of the test item was assessed according to OECD TG 404. Three rabbits were exposed to 0.5 mg test item under semi-occlusive conditions. Slight brown staining produced by the colour of the test item on the treated skin was observed in all animals at the 1-hour reading and persisted up to the 48- or 72-hour reading. The test item did not elicit any skin reactions at the application site of any animal at any of the observation times (all scores 0). The individual mean score for erythema/eschar and oedema for each of the three animals was therefore 0.
Reference
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:
- 2006
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study (OECD TG 405) performed under GLP
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Harlan Netherlands BV, Horst, The Netherlands
- Age at study initiation: 12-15 weeks
- Housing: Individually in stainless steel cages equipped with feed hoppers and drinking water bowls.
- Diet: Pelleted standard Provimi Kliba 3418 rabbit maintenance diet (batch no. 85/05; provided by Provimi Kliba AG, CH-4303 Kaiseraugst); ad libitum
- Water: Community tap water from Füllinsdorf, ad libitum
- Acclimation period: 4 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 17-23
- Humidity (%): 30-70
- Air changes (per hr): 10-15
- Photoperiod (hrs dark / hrs light): 12/12 - Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- 0.1 g
- Duration of treatment / exposure:
- single application, the treated eyes were not rinsed after instillation
- Observation period (in vivo):
- 7 days
- Number of animals or in vitro replicates:
- 3 (1 male, 2 females)
- Details on study design:
- TOOL USED TO ASSESS SCORE:
Eye examinations were made with a Varta Cliptrix diagnostic-lamp (Roth AG, Reinach/Switzerland).
SCORING SYSTEM:
Grading of Ocular Lesions according to COMMISSION DIRECTIVE 2004/73/EC, APRIL 29, 2004; comparable to Draize system
CORNEA
Opacity: degree of density (area most dense taken for reading)
No ulceration or opacity..............................................................................................................0
Scattered or diffuse areas of opacity (other than slight dulling of normal luster),
details of iris clearly visible.........................................................................................................1
Easily discernible translucent area, details of iris slightly obscured...................................2
Nacreous area, no details of iris visible, size of pupil barely discernible............................3
Opaque cornea, iris not discernible through the opacity......................................................4
IRIS
Normal............................................................................................................................................0
Markedly deepened rugae, congestion, swelling, moderate circumcorneal hyperemia, or injection, any of these or combination of any thereof, iris still reacting to light (sluggish reaction is positive).......................................................................1
No reaction to light, hemorrhage, gross destruction (any or all of these)..........................2
CONJUNCTIVAE
Redness (refers to most severe reading of palpebral and bulbar conjunctivae when compared with control eye)
Blood vessels normal....................................................................................................................0
Some blood vessels definitely hyperemic (injected)................................................................1
Diffuse, crimson color, individual vessels not easily discernible..........................................2
Diffuse beefy red...........................................................................................................................3
Chemosis: lids and/or nictitating membranes
No swelling.....................................................................................................................................0
Any swelling above normal (including nictitating membranes)............................................1
Obvious swelling with partial eversion of lids..........................................................................2
Swelling with lids about half-closed..........................................................................................3
Swelling with lids more than half-closed..................................................................................4 - Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 24-48-72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: reversibility not applicable
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- other: 24-48-72 h
- Score:
- 0
- Max. score:
- 2
- Reversibility:
- other: reversibility not applicable
- Irritation parameter:
- conjunctivae score
- Remarks:
- (redness)
- Basis:
- animal: #1 and #2 each
- Time point:
- other: mean of 24-48-72 h
- Score:
- 0
- Max. score:
- 3
- Reversibility:
- other: reversibility not applicable
- Irritation parameter:
- conjunctivae score
- Remarks:
- (redness)
- Basis:
- animal #3
- Time point:
- other: mean of 24-48-72 h
- Score:
- 1
- Max. score:
- 3
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- other: 24-48-72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: reversibility not applicable
- Irritant / corrosive response data:
- The mean score was calculated across 3 scoring times (24, 48 and72 hours after instillation) for each animal for corneal opacity, Iris, redness and chemosis of the conjunctivae, separately. The individual mean scores for corneal opacity and iris were 0.00 for all three animals. The individual mean scores for the conjunctivae were 0.00,0.00 and 1.00 for reddening and 0.00 for chemosis for all animals, respectively. Very slight corneal opacity affecting the whole area was noted in all treated animals 1 hour after instillation but was no langer present at the 24-hour reading. No abnormal findings were noted in the iris of any of the animals.
Slight reddening of the conjunctivae was noted in all animals one hour after treatment and persisted until the 72-hour reading in one animal.
Slight reddening of the sclerae was noted in one animal from 1 hour after treatment to the 72-hour observation.
Slight ocular discharge was noted in all animals at the 1-hour reading.
No abnormal findings were observed in the treated eye of any animal7 days after treatment. - Other effects:
- No clinical signs of systemic toxicity were observed in the animals during the study and no mortality occurred.
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The test item did not induce significant or irreversible damage to the rabbit eye in this study according to OECD test guideline no. 405 and GLP conditions.
- Executive summary:
The eye irritating potential of the test item was assessed according to OECD TG 405. Three rabbits were exposed to 0.1 mg test item. The mean score was calculated across 3 scoring times (24, 48 and72 hours after instillation) for each animal for corneal opacity, Iris, redness and chemosis of the conjunctivae, separately. The individual mean scores for corneal opacity and iris were 0.00 for all three animals. The individual mean scores for the conjunctivae were 0.00,0.00 and 1.00 for reddening and 0.00 for chemosis for all animals, respectively. Very slight corneal opacity affecting the whole area was noted in all treated animals 1 hour after instillation but was no langer present at the 24-hour reading. No abnormal findings were noted in the iris of any of the animals.
Slight reddening of the conjunctivae was noted in all animals one hour after treatment and persisted until the 72-hour reading in one animal.
Slight reddening of the sclerae was noted in one animal from 1 hour after treatment to the 72-hour observation.
Slight ocular discharge was noted in all animals at the 1-hour reading.
No abnormal findings were observed in the treated eye of any animal 7 days after treatment.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Justification for classification or non-classification
No classification, as no adverse effects were observed
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