Registration Dossier
Registration Dossier
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 209-548-7 | CAS number: 585-07-9
- 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:
- January 1994
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Referenceopen allclose all
- Reference Type:
- other: Amendment to study report
- Title:
- Unnamed
- Year:
- 1 995
- Report date:
- 1995
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 994
- Report date:
- 1994
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Version / remarks:
- 1992
- GLP compliance:
- yes
Test material
- Reference substance name:
- tert-butyl methacrylate
- EC Number:
- 209-548-7
- EC Name:
- tert-butyl methacrylate
- Cas Number:
- 585-07-9
- Molecular formula:
- C8H14O2
- IUPAC Name:
- tert-butyl 2-methylprop-2-enoate
Constituent 1
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source (supplier): BASF AG
- Lot number of test material: LAB.J.NO. 387
- Purity: not specifed
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: Refrigerator, exclusion of light
- Stability and homogeneity of the test material in the vehicle/solvent under test conditions and during storage: The stability of the test substance over the study period was proved by reanalysis. The result was reported in the form of an amendment (12 January 1995). According to the analytical determination, dated December 07, the test substance was stable over the study period. The sample appeared to be homogeneous.
FORM AS APPLIED IN THE TEST
- The test substance was applied in a single dose to the tact untreated skin. The test patch was secured in position with a semiocclusive dressing.
Test animals
- Species:
- rabbit
- Strain:
- Vienna White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Gaukler, Offenbach/Main, D
- Age at study initiation: young adult, not further specified
- Weight at study initiation: 3.35 - 3.82 kg
- Housing: single
- Diet: Kliba Labordiaet 341, Klingenthalmuehle AG, Kauseraugst, Switzerland, about 130 g per animal per day
- Water: about 250 ml tap water per animal per day
- Acclimation period: at least 1 week
ENVIRONMENTAL CONDITIONS
- Temperature: 20-24°C
- Humidity: 30-70%
- Air changes (per hr): not specified
- Photoperiod (hrs dark / hrs light): 12 h/12 h (6.00 a.m.- 6.00 p.m./6.00 p.m.- 6.00 a.m.)
IN-LIFE DATES: not specified
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- clipped
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: Yes, untreated skin sites of the same animal
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): The test patch (2.5 cm x 2.5 cm) was moistened with a dose of 0.5 ml of the unchanged liquid test substance. - Duration of treatment / exposure:
- 4 h
- Observation period:
- 15 d
- Number of animals:
- 3
- Details on study design:
- TEST SITE
- Area of exposure: upper third of the back or flanks
- % coverage: 2.5 x 2.5 cm
- Type of wrap if used: Idealbinde, Pfaelzische Verbandsstoff-Fabrik, Kaiserslautern, Germany and Fixomull stretch (adhesive fleece), Beiersdorf AG
REMOVAL OF TEST SUBSTANCE
- Washing (if done): The test substance wa sremoved at the end of the exposure period with Lutrol (=Polyethylenglykol) pure and Lutrol/water 1:1
- Time after start of exposure: 4 h
SCORING SYSTEM: OECD Draize
- for detailed information please refer to section "Any other information on materials and methods incl. tables"
OBSERVATION TIME POINTS: 1 h, 24 h, 48 h, 72 h, 8 d and 15 d after removal of the patch
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Remarks:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 3
- Max. score:
- 4
- Reversibility:
- fully reversible within: 15 days
- Remarks on result:
- positive indication of irritation
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Remarks:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- fully reversible within: 15 d
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Remarks:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 2.3
- Max. score:
- 4
- Reversibility:
- fully reversible within: 15 d
- Remarks on result:
- positive indication of irritation
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 2.43
- Max. score:
- 4
- Reversibility:
- fully reversible within: 15 d
- Remarks on result:
- positive indication of irritation
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Remarks:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 d
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Remarks:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 d
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Remarks:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 d
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 d
- Remarks on result:
- no indication of irritation
- Irritant / corrosive response data:
- The numerical scores awarded to the dermal reactions of each animal elicited by the test substance are given in Table 1 in section "Any other information on results incl. tables".
Any other information on results incl. tables
Table 1: Dermal reactions elicited by the test substance.
Exposition: | 4 h | |||
Animal | Reading | Erythema | Edema | Symptoms |
1 | 1 h | 2 | 1 |
|
2 | 1 h | 1 | 0 |
|
3 | 1 h | 2 | 1 |
|
1 | 24 h | 3 | 1 |
|
2 | 24 h | 2 | 0 |
|
3 | 24 h | 2 | 0 |
|
1 | 48 h | 3 | 1 |
|
2 | 48 h | 2 | 0 |
|
3 | 48 h | 2 | 0 |
|
1 | 72 h | 3 | 1 |
|
2 | 72 h | 2 | 0 |
|
3 | 72 h | 3 | 0 |
|
1 | 8 d | 1 | 0 | Scaling |
2 | 8 d | 1 | 0 | Scaling |
3 | 8 d | 1 | 0 | Scaling |
1 | 15 d | 0 | 0 |
|
2 | 15 d | 0 | 0 | Scaling |
3 | 15 d | 0 | 0 |
|
mean | 24 - 72 h | 2.44 | 0.33 |
|
Applicant's summary and conclusion
- Interpretation of results:
- Category 2 (irritant) based on GHS criteria
- Conclusions:
- Under the test conditions chosen and considering the described findings the test substance gives indication of an irritant property to the skin.
- Executive summary:
Acute dermal irritation or corrosion to skin was evaluated in a GLP compliant study according to the OECD TG 404. Thereby, test patches containing 0.5 ml of the test substance were applied by a single topical application to the intact skin of three white Vienna rabbits for 4 hours under semiocclusive dressing. The skin sites were evaluated for erythema/eschar and edema formation 1 h, 24 h, 48 h, 72 h, 8 d and 15 d following removal of the patches. The average score (24 to 72 hours) for irritation was calculated to be 2.4 for erythema and 0.3 for edema. Signs of skin irritation such as erythema and edema were reversible within 15 days after removal of the patches, while scaling was still present in one animal at study termination. Under the test conditions chosen and considering the described findings the test substance gives indication of an irritant property to the skin.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
