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EC number: 215-691-6 | CAS number: 1344-28-1
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin 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 restrictions
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 979
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- : longer duration of exposure (24 versus 4 hours); limited details on test material and test conditions
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Aluminium oxide
- EC Number:
- 215-691-6
- EC Name:
- Aluminium oxide
- Cas Number:
- 1344-28-1
- Molecular formula:
- Al2O3
- IUPAC Name:
- oxo[(oxoalumanyl)oxy]alumane
- Details on test material:
- - Name of test material (as cited in study report): aluminium oxide (TBH) coded AK 43/79
-purple coloured solid
- Analytical purity: no data
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- other: intact or abraded skin
- Vehicle:
- not specified
- Controls:
- no
- Amount / concentration applied:
- 0.5 g of the solid test substance was brought into contact with the intact or abraded skin under a surgical patch measuring 1 inch Χ 1 inch.
- Duration of treatment / exposure:
- 24 hours
- Observation period:
- 24 hours and 72 hours after the substance application
- Number of animals:
- 6 rabbits were treated on intact skin and 6 on abraded skin.
- Details on study design:
- TEST SITE
- Area of exposure: the hair was removed from the backs of the animals with an electric clipper avoiding abrasions. The test material was placed under a surgical patch 1 inch Χ 1 inch (2.5 cm Χ 2.5 cm) on intact or abraded skin.
- Type of wrap if used: surgical patch. The patches were fixed to the application site with adhesive tape. The entire trunk of the animals was wrapped with an impervious material to keep the patches in place.
SCORING SYSTEM: Draize scoring system
The abrasions were “minor incisions through the stratum corneum, but not sufficiently deep to disturb the derma or to produce bleeding.”
The patches were fixed to the application site with adhesive tape. The entire trunk of the animals was wrapped with an impervious material to keep the patches in place
After exposure for 24 hours, the patches and the test material were removed (no information was provided on washing of the skin after patch removal.)
Skin lesions were evaluated at the time of patch and material removal and 48 hours later (24 and 72 hours after the application)
Scoring systems applied:
-24 hours after application -method of Draize (J. Pharmocol. 82 (1944) 377-390).
-72 hours after application – CIVO grading system (because the Draize scoring system does not describe scaliness and necrosis)
Evaluation of skin reactions (Draize, 1944) Value
A. Erythema and eschar formation
No erythema 0
Very slight erythema (barely perceptible) 1
Well-defined erythema 2
Moderate to severe erythema 3
Severe erythema (beet redness) to slight eschar formation (injuries in depth) 4
B. Edema formation
No edema 0
Very slight edema (barely perceptible) 1
Slight edema (edges of area well defined by definite raising) 2
Moderate edema (raised approximately 1 mm) 3
Severe edema (raised more than 1 mm and extending beyond the area of exposure) 4
Evaluation of skin reactions (CIVO) Value
No reaction at all 0
Very slight scaliness 1
Distinct scaliness or very slight incrustation 2
Distinct incrustation 3
Severe incrustation 4
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- of 6 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: reversibility: not applicable
- Remarks:
- No 48 h data are available for calculation of mean scores, the 48 h values were assumed to be the same as those at 24 h (worst case assumption: persistence of effects seen at 24 h over 48 h)
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: reversibilty: not applicable
- Remarks:
- No 48 h data are available for calculation of mean scores, the 48 h values were assumed to be the same as those at 24 h (worst case assumption: persistence of effects seen at 24 h over 48 h)
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: reversibilty: not applicable
- Remarks:
- No 48 h data are available for calculation of mean scores, the 48 h values were assumed to be the same as those at 24 h (worst case assumption: persistence of effects seen at 24 h over 48 h)
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 72 h
- Remarks:
- No 48 h data are available for calculation of mean scores, the 48 h values were assumed to be the same as those at 24 h (worst case assumption: persistence of effects seen at 24 h over 48 h)
- Irritation parameter:
- erythema score
- Basis:
- animal #4
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: reversibilty: not applicable
- Remarks:
- No 48 h data are available for calculation of mean scores, the 48 h values were assumed to be the same as those at 24 h (worst case assumption: persistence of effects seen at 24 h over 48 h)
- Irritation parameter:
- erythema score
- Basis:
- animal #5
- Time point:
- 24/48/72 h
- Score:
- 0.67
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 h
- Remarks:
- No 48 h data are available for calculation of mean scores, the 48 h values were assumed to be the same as those at 24 h (worst case assumption: persistence of effects seen at 24 h over 48 h)
- Irritation parameter:
- erythema score
- Basis:
- animal #6
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: reversibilty: not applicable
- Remarks:
- No 48 h data are available for calculation of mean scores, the 48 h values were assumed to be the same as those at 24 h (worst case assumption: persistence of effects seen at 24 h over 48 h)
- Irritant / corrosive response data:
- Overall, the test material caused slight erythema in 2 of the 12 rabbits (one - 24 hours after application, and the other - 72 hours after application).
- Other effects:
- Clinical signs of toxicity were not reported
Any other information on results incl. tables
Individual and average skin reaction scores
1) Intact skin
--------------------------------------------------------------------------------------------
Rabbit number 24 hour 72 hour
A-B A-B
---------------------------------------------------------------------------------------------
8416 0-0 0-0
8417 0-0 0-0
8418 0-0 1-0
8419 0-0 0-0
8420 1-0 0-0
8421 0-0 0-0
--------------------------------------------------------------------------------------------
Average 0.2 0.2
--------------------------------------------------------------------------------------------
2) Abraded skin
--------------------------------------------------------------------------------------------
Rabbit number 24 hour 72 hour
A-B A-B
---------------------------------------------------------------------------------------------
8410 0-0 0-0
8411 0-0 0-0
8412 0-0 0-0
8413 0-0 0-0
8414 0-0 0-0
8415 0-0 0-0
--------------------------------------------------------------------------------------------
Average 0.0 0.0
--------------------------------------------------------------------------------------------
A – erythema; B – edema
Overall, the test material caused slight erythema in 2 of the 12 rabbits (one - 24 hours after application, and the other - 72 hours after application). Conclusion: Due to the slight character of the observed effects the test substance does not have to be classified according to the criteria of the DSD and the CLP regulation.
Applicant's summary and conclusion
- Interpretation of results:
- other: CLP/EU GHS criteria not met, no classification required according to Regulation (EC) No. 1272/2008
- Conclusions:
- The observed slight erythema effects do not lead to a classification for the test item. Therefore AK 43/79 is not considered to be a primary skin irritant.
- Executive summary:
This study conducted for Degussa corporation investigated dermal irritation effects of aluminium oxide in New Zealand White albino rabbits. 0.5 g of the test substance was placed on the intact or abraded skin of the rabbits under a surgical patch measuring 2.5 Χ 2.5 cm. Six rabbits had intact skin and six rabbits abraded skin. The exposure continued for 24 hours (a 4 hour exposure is recommended by OECD 404), and skin lesions were scored immediately after patch removal and 48 hours later (24 and 72 hours after the application of the test material). Two sets of scoring criteria were used: Draize (1944) - 24 hours after the material application and CIVO - 72 hours after the application.
Insufficient information was provided on the test material and in what form it was applied to the skin. No information was provided on animal husbandry. Slight erythema was observed on the intact skin of 2 animals (one 24 hours after the substance application and the other 72 hours after application). No signs of skin irritation were observed on the abraded skin at any time. The overall primary irritation score from the study (0.2) would not lead to classification.
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