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Diss Factsheets
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EC number: 230-391-5 | CAS number: 7085-85-0
- 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 sensitisation
Administrative data
- Endpoint:
- skin sensitisation
- Remarks:
- in vivo
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Acceptable, well-documented publication which meets basic scientific principles
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 983
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Various methods tested
- GLP compliance:
- not specified
- Type of study:
- other: Polak method / Split adjuvant method / Maximization method / Epicutaneous methods
Test material
- Reference substance name:
- Mecrilate
- EC Number:
- 205-275-2
- EC Name:
- Mecrilate
- Cas Number:
- 137-05-3
- Molecular formula:
- C5H5NO2
- IUPAC Name:
- methyl 2-cyanoacrylate
- Test material form:
- other: emulsion or solution
- Details on test material:
- Different acrylic compounds have been tested in this study:
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Hartley
- Sex:
- male/female
- Details on test animals and environmental conditions:
- ANIMALS:
Outbred Hartley strain guinea-pigs of either sex weighing 400-500 g were used. The animals were from stocks bred either at the Royal College of Surgeons or from David Hall, Newchurch, Staffordshire, England. The animals were fed a Labsure RGP diet (F. Dixon & Son, Ware, Hertfordshire) liberally supplemented with cabbage and hay.
Results and discussion
- Positive control results:
- no data
Any other information on results incl. tables
RESULTS
Previous work has shown that, in our hands, the Polak method of sensitization was better than the maximization or split adjuvant methods in
inducing sensitivity to the metals nickel and zirconium. Consequently, attempts were made, using the Polak method, to sensitize guinea pigs to 21 different acrylic compounds.
Table 1 Iists the chemicals that induced contact sensitivity to a non-irritant skin test dose. As can be seen, from the time of the first positive skin test, acrylic acid, tripropylene glycol diacrylate and pentaerythritol triacrylate (PETA) appeared to be not as strong sensitizers as the other 5 compounds. This difference could, however, be the result of using different molar concentrations.
TABLE 1: Contact skin reactions in guinea pigs immunized by the Polak method:
Compound |
No. of animals |
Time of first positive skin test |
Acrylic acid |
6 |
28 days |
Methyl acrylate |
15 |
7 days |
Butyl acrylate |
11 |
7 days |
2 -ethyl hexyl acrylate |
6 |
7 days |
1 -6 -hexanediol diacrylate |
6 |
7 days |
Tripropylene glycol diacrylate |
6 |
28 days |
Trimethylol propane triacrylate |
11 |
7 days |
Pentaerythritol triacrylate |
6 |
14 days |
Below listed are the chemicals that, during the 3 months of the experiment. never induced a contact sensitivity skin reaction to the immunizing chemical:
Methacrylic acid
Trichloracrylic acid
Methyl methacrylate
Butyl methacrylate
2-hydroxyethyl methacrylate
Tetrahydrofurfuryl methacrylate
Ethoxy ethyl methacrylate
Allyl methacrylate
Triethylene glycol dimethacrylate
Ethylene glycol dimethacrylate
Trimethyl propane trimethacrylate
Methyl cyanoacrylate
Butyl cyanoacrylate
Attempts were made to sensitize guinea pigs to methyl and butyl acrylate and methyl methacrylate using the split adjuvant and maximization
techniques. Although the contact skin reactions were not as strong as when the animals were immunized using the Polak method, all the guinea pigs immunized by the split adjuvant method, showed positive reactions to butyl acrylate and 4 out of 6 to methyl acrylate on the first skin test.
Using the maximization method, 30% of the animals developed contact reactions to methyl acrylate on day 21. This did not increase with subsequent skin testing. Again, it was not possible to induce contact sensitivity skin reactions to methyl methacrylate using either immunization
protocol. Because of reports that the methacrylates are volatile, closed patch tests were performed on occasions, but this still did not induce positive skin reactions.
Contact reactions develop in humans due to continuous and repeated exposure to the acrylic compound through the skin. In consequence, 2
methods of epicutaneous sensitization were developed which involved repeated exposure to the chemical. The epicutaneous method A, which involved a total of 6 exposures, was not able to induce contact skin reactions even to methyl acrylate. However. epicutaneous method B induced good contact sensitivity to both trimethylol propane triacrylate and pentaerythritol triacrylate. 4 out of 6 guinea pigs were also sensitized to methyl acrylate and 3 out of 6 to butyl acrylate using this method. Again, it was not possible, in this laboratory, to induce contact reactions to methyl methacrylate even when in one experiment the animals were exposed to methyl methacrylate for 3 weeks (15 exposures) instead of 2 weeks.
ADDENDUM
A recent paper by Van der Walle el aI. (Contact Dermatitis 8, 223 -235, 1982) reports the successful induction of contact sensitivity skin reactions to methyl methacrylate in guinea pigs. Using the guinea pig maximization test and a Freund's complete adjuvant test, they induced contact reactions in 2 out of 10 and 2 out of 8 guinea pigs respectively. The reason for this difference could be that Van der Walle and his colleagues immunized each guinea pig with either 25 or 20 mg of methyl methacrylate, whereas in this study between 250 µg and 4 mg of the chemical per animal were used in the intradermal immunization procedures.
Evidently, if sufficient chemical is used for immunization, a % of guinea pigs will give contact sensitivity reactions to methyl methacrylate.
However, it does not sensitize guinea pigs as easily as do the comparable acrylate compounds.
Applicant's summary and conclusion
- Interpretation of results:
- not sensitising
- Remarks:
- Migrated information
- Conclusions:
- Methyl cyanoacrylate did not induce contact sensitivity in the respective tests.
- Executive summary:
SUMMARY
Among many different acrylic compounds, methyl cyanoacrylate and butyl cyanoacrylate were tested for their skin sensitising properties with the following methods:
- Polak method
- Split adjuvant method
- Maximization method (modified)
- Epicutaneous methods (Levene and Draize (modified))
Both, methyl cyanoacrylate and butyl cyanoacrylate were shown to not be skin sensitisers in these tests.
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