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: 700-487-6 | CAS number: -
- 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 vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2010-10-05 - 2010-10-12
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study, GLP
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 010
- Report date:
- 2010
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- other: EU B.46
- Deviations:
- yes
- Remarks:
- The test item was brought onto a nylon mesh on a microscope slide. Instead of incubating it for 30 minutes at 37 °C, the test item was incubated for 60 minutes at 37 °C. This deviation can be seen as uncritical.
- Qualifier:
- according to guideline
- Guideline:
- other: EU B.46
- Deviations:
- yes
- Remarks:
- The plate was not left to stand over night at room temperature. The plate was shaken for two hours and then the tissues were pierced with an injection needle.
- Qualifier:
- according to guideline
- Guideline:
- other: EU B.46
- Deviations:
- yes
- Remarks:
- Within the pre-tests and the main study 25±6 mg of the test item were used instead of 25mg. This deviation can be seen as uncritical since it was very difficult to weigh an exact amount of test item because of its resin appearance.
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- reaction products of diglycidyl ether bisphenol F (DGEBF) and oligomeric phenol diglycidyl ethers with acrylic acid
- EC Number:
- 700-487-6
- Molecular formula:
- Not applicable.
- IUPAC Name:
- reaction products of diglycidyl ether bisphenol F (DGEBF) and oligomeric phenol diglycidyl ethers with acrylic acid
- Details on test material:
- Name: Epoxy half acrylate
Constituent 1
Test animals
- Species:
- other: Human Skin Model
Test system
- Type of coverage:
- open
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Duration of treatment / exposure:
- 60 min
- Observation period:
- 60 min
Results and discussion
In vitro
Results
- Irritation / corrosion parameter:
- other: other: % Formazan Production
- Value:
- 12.2
- Remarks on result:
- other:
- Remarks:
- Basis: mean. Time point: 60 min. Max. score: 50.0. Reversibility: no data. (migrated information)
Any other information on results incl. tables
For the test item and the positive control, the following percentage values of formazan production were calculated in comparison to the negative control:
% Formazan Production
Designation |
Test item |
Positive Control |
% Formazan production (Tissue 1) |
12.6% |
7.0% |
% Formazan production (Tissue 2) |
12.9% |
7.3% |
% Formazan production (Tissue 3) |
11.0% |
7.7% |
% Formazan production Mean |
12.2% |
7.3% |
Applicant's summary and conclusion
- Interpretation of results:
- irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: other: CLP, EU GHS (Regulation (EC) No 1272/2008)
- Conclusions:
- The test item is considered irritant.
After the treatment, the relative absorbance values were decreased to 12.2%. This value is well below the threshold for irritation (50%).
The optical density of the negative control was well within the required acceptability crite-rion of 1.0 < mean OD < 2.5. The positive control induced a decrease in the relative absorbance as compared to the negative control to 7.3% (required: = 20%) for thus ensuring the validity of the test system. Variation within replicates was within the accepted range for negative control, positive control and test item.
For these reasons, the result of the test is considered valid. - Executive summary:
One valid experiment was performed. Three tissues of the human skin model EpiDermTM were treated with Epoxy half acrylate for 60 minutes.
25 mg of the liquid test item (using a nylon mesh) were applied to each tissue and spread to match the tissue size.
DPBS-buffer was used as negative control, 5% SDS-solution was used as positive control.
After treatment with the negative control, the absorbance values were within the required acceptability criterion of 1.0 < mean OD < 2.5. The positive control showed clear irritating effects. Variation within tissues was acceptable (< 18%).
After the treatment with the test item, the relative absorbance values were reduced to 12.2 %. This value is well below the threshold for irritation potential (50%). Therefore, Epoxy half acrylate is considered as irritant in the Human Skin Model Test.
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.

EU Privacy Disclaimer
This website uses cookies to ensure you get the best experience on our websites.