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EC number: 817-217-9 | CAS number: 116280-23-0
- 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: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- From 28/07/2011 to 14/09/2011
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study
- Remarks:
- "ISO 10993-10: 2010 Standard, Biological Evaluation of Medical Devices, Part 10: Tests for Irritation and Skin Sensitization, Pages 18-26, GLP" comparable to OECD Guideline 406
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 011
- Report date:
- 2011
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- GLP compliance:
- yes
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- Guinea pig maximisation test already available from 2011 in compliance with U.S. Food and Drug Administration Good Laboratory Practice (GLP) regulations set forth in 21 CFR part 58.
Test material
- Reference substance name:
- 1-(2-ethoxy-2-oxoethyl) 3-ethyl 2-methylidenepropanedioate
- EC Number:
- 817-217-9
- Cas Number:
- 116280-23-0
- Molecular formula:
- C10H14O6
- IUPAC Name:
- 1-(2-ethoxy-2-oxoethyl) 3-ethyl 2-methylidenepropanedioate
- Test material form:
- liquid
- Details on test material:
- - Name of test material (as cited in study report): Bond.Ease™ Topical Skin Adhesive (polymerized)
- Batch no.: 10312101
- Physical state: Liquid
- Purity: >96%
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Hartley
- Sex:
- male
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Charles River Laboratories
- Age: Healthy young adults were used.
- Weight Range: All animals weighed between 300 and 500 g upon assignment to the test.
- Housing: Animals were housed in solid bottom cages with contact bedding and up to two guinea pigs per cage. Housing density complied with AAALAC International recommendations. The test and negative control animals were housed separately.
- Diet: Animals were supplied with certified commercial guinea pig feed, ad libitum. No known contaminants present in the feed were expected to interfere with the test results.
- Water: Potable water was obtained from the St. Paul municipal water supply. No known contaminants present in the water were expected to interfere with the test results.
- Receipt: Animals were received on 07/27/11 according to WuXi AppTec SOP: ILS-0092. Each animal was examined for signs of disease and injury. The animals were acclimated for a minimum of 5 days under the same conditions as the actual test.
ENVIRONMENTAL CONDITIONS
The environmental conditions in the animal rooms were set to be maintained according to WuXi AppTec SOP: ILS-0018. The temperature and photo-period were set to meet the AAALAC International recommendations for these species. The laboratory and animal rooms were maintained as limited-access facilities.
Study design: in vivo (non-LLNA)
Induction
- Route:
- intradermal and epicutaneous
- Vehicle:
- other: 0.9% Normal Saline / Cottonseed Oil
Challenge
- Route:
- epicutaneous, occlusive
- Vehicle:
- other: 0.9% Normal Saline / Cottonseed Oil
- No. of animals per dose:
- 11 (test group)
6 (control group) - Details on study design:
- MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: one intradermal exposure and one epidermal exposure
- Exposure period: First induction week: intradermal induction/ Second induction week: epidermal induction
- Test groups:
Intradermal Induction:
1) Syringe 1: 0.1 ml of FCA + 0.9% Sterile Saline - Ratio: 1:1 (v/v)
2) Syringe 2: 0.1 mL of Test Extract
3) Syringe 3: 0.1 mL of FCA + 0.9% Sterile Saline (1:1) + Test Extract - Ratio: 1:1 (v/v)
Epidermal Induction: 0.3 ml of freshly prepared test article extract.
- Control group:
Intradermal Induction:
1) Syringe 1: 0.1 ml of FCA + 0.9% Sterile Saline - Ratio: 1:1 (v/v)
2) Syringe 2: 0.1 mL of Control Vehicle
3) Syringe 3: 0.1 mL of FCA + 0.9% Sterile Saline (1:1) + Control Vehicle - Ratio: 1:1 (v/v)
Epidermal Induction: 0.3 ml of freshly prepared control vehicle.
- Site: The intradermal induction was performed on the shaved shoulder region of the guinea pigs (on each side of the dorsal mid-line). The epidermal induction was performed over the injection sites.
- Frequency of applications: One week after the intradermal induction injections the epidermal induction application was performed.
- Duration:
Three pairs of intradermal injections made simultaneously for the intradermal induction.
Closed patch exposure for 48 hours for the epidermal induction.
- Concentrations:
100% test article extract
100% control vehicle
B. CHALLENGE EXPOSURE
- No. of exposures: single
- Day(s) of challenge: 14 days after completion of epidermal induction.
- Exposure period: 24 hours
- Test groups: 0.3 ml of freshly prepared test article extract
- Control group: 0.3 ml of freshly prepared control vehicle
- Site: right flank (test article extract) / left flank (Control vehicle)
- Concentrations:
100% test article extract
100% control vehicle
- Evaluation (hr after challenge): 24 hours and 48 hours after removal of the dressings. - Positive control substance(s):
- yes
- Remarks:
- Dinitrochlorobenzene (DNCB)
Results and discussion
- Positive control results:
- For the Induction I and Induction II phases, 0.3% dinitrochlorobenzene (DNCB), a known sensitizer, in ethanol is used. For the challenge phase, 0.15% DNCB in acetone is used. The negative control animals are exposed to the appropriate vehicle (acetone is used for the challenge and ethanol is used for the Inductions I and II) only.
Animals in the positive control test group exhibited moderate and confluent erythema to intense erythema and swelling at the challenge sites (scores of 2-3 during 48 hour score) and all of the animals in the negative control group exhibited discrete or patchy erythema at the challenge sites (score of 1 during 48 hour score) when treated with the 0.15% w/v mixture of DNCB in acetone. Since the sensitization results are based on the scores of the test group subtracted by the scores of the negative control group, the score of 1 for the negative control animals are subtracted from that of the
scores of 2-3, observed for the positive control test group. Therefore, all reactions in the positive control test group are considered to be sensitization reactions. Based on the results obtained, this test methodology demonstrated dermal sensitization in guinea pigs using DNCB, a known sensitizer.
In vivo (non-LLNA)
Resultsopen allclose all
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 100% test substance
- No. with + reactions:
- 0
- Total no. in group:
- 11
- Clinical observations:
- No visible change - No erythema and edema
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 100% test substance
- No. with + reactions:
- 0
- Total no. in group:
- 11
- Clinical observations:
- No visible change - No erythema and edema
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 100% control vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 6
- Clinical observations:
- No visible change - No erythema and edema
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 100% control vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 6
- Clinical observations:
- No visible change - No erythema and edema
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 0.15% DNCB in acetone
- No. with + reactions:
- 11
- Total no. in group:
- 11
- Clinical observations:
- Discrete or patchy erythema to intense erythema and swelling (scores of 1, 2, 3)
- Remarks on result:
- positive indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 0.15% DNCB in acetone
- No. with + reactions:
- 11
- Total no. in group:
- 11
- Clinical observations:
- Moderate and confluent erythema to intense erythema and swelling (scores 2-3)
- Remarks on result:
- positive indication of skin sensitisation
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- None of the negative control animals challenged with the control vehicle were observed with a sensitization response greater than '0'. None of the animals challenged with the test article extracts were observed with a sensitization response greater than '0'. The normal saline extract of the test material had a sensitization response of '0' under valid test conditions. The cottonseed oil extract of the test material had a sensitization response of '0' under valid test conditions. Under the conditions of this protocol, the test article did not elicit a sensitization response.
- Executive summary:
This study was conducted in compliance with U.S. Food and Drug Administration Good Laboratory Practice (GLP) regulations set forth in 21 CFR, Part 58, in accordance with ISO 10993 -10:2010 Biological Evaluation of Medical Devices, Part 10- Tests for Irritation and Skin Sensitization, pages 10 -26 (Comparable to OECD Guideline 406).
Method used: Guinea pig maximisation test.
This test was designed to evaluate the allergenic potential or sensitizing capacity of the test article.
Summary design: Eleven test guinea pigs (per extract) were injected with the test article extract and FCA, and six guinea pigs (per extract) were injected with the corresponding control blank and FCA. On Day 6, the dorsal site was reshaved and SLS in mineral oil was applied. The day after the SLS application, the test animals were topically patched with the appropriate test extract and the control animals were patched with the corresponding control blank. The patches were removed after 48 ± 2 hours of exposure. Following an approximate two-week rest period, the animals were topically patched with the appropriate test extract and corresponding control blank. The patches were removed after 24 ± 2 hours of exposure. The dermal patch sites were observed for erythema and edema 24 ± 2 and 48 ± 2 hours after patch removal. Each anim al was assessed for a sensitization response based upon the dermal scores. The test results were based upon the percentage of animals exhibiting a sensitization response.
Species/Strain: Albino guinea pigs (Cavia porcellus), Hartley strain (specific pathogen free), male.
Results/Conclusion:
None of the negative control animals challenged with the control vehicle were observed with a sensitization response greater than '0'. None of the animals challenged with the test article extracts were observed with a sensitization response greater than '0'. The normal saline extract of the test material had a sensitization response of '0' under valid test conditions. The cottonseed oil extract of the test material had a sensitization response of '0' under val id test conditions. Under the conditions of this protocol, the test article did not elicit a sensitization response.
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