Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
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: 218-407-9 | CAS number: 2144-53-8
- 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This study was selected as the key study because the information provided for the hazard endpoint is sufficient for the purpose of classification and labelling and/or risk assessment.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 008
- Report date:
- 2008
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- no
- Remarks:
- This study was conducted according to guideline in effect at time of study conduct.
- Qualifier:
- according to guideline
- Guideline:
- other: U.S. EPA Health Effects Test Guidelines OPPTS 870.2400
- Deviations:
- no
- Remarks:
- This study was conducted according to guideline in effect at time of study conduct.
- GLP compliance:
- yes
Test material
- Reference substance name:
- 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl methacrylate
- EC Number:
- 218-407-9
- EC Name:
- 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl methacrylate
- Cas Number:
- 2144-53-8
- Molecular formula:
- C12H9F13O2
- IUPAC Name:
- 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl 2-methylprop-2-enoate
- Details on test material:
- - Purity: 97.59%
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Age at study initiation: Young adult
- Weight at study initiation: 2366, 2518, 2512 g
- Housing: Singly in suspended stainless steel, wire-mesh cages. Litter paper was placed beneath the cage and was changed at least three times per week.
- Diet (e.g. ad libitum): Pelleted Purina Rabbit Chow #5326; daily amount not reported
- Water (e.g. ad libitum): filtered tap water supplied ad libitum by an automatic water dispensing system.
- Acclimation period: 14 or 20 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 19-21ºC
- Humidity (%): 51-65%
- Air changes (per hr): Not reported
- Photoperiod (hrs dark / hrs light): 12-hour light/dark cycle
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: The left eye of each rabbit was not treated with the test substance and served as a control.
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1 mL - Duration of treatment / exposure:
- Single exposure
- Observation period (in vivo):
- 1, 24, 48, and 72 hours after treatment.
- Number of animals or in vitro replicates:
- 3
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing (if done): Treated and control eyes of all rabbits remained unwashed.
SCORING SYSTEM: Draize Scale
TOOL USED TO ASSESS SCORE: Illumination and fluorescein stain (24-hour evaluation).
The study was conducted in a stepwise fashion. Initially, one-tenth of a millilitre of the test substance was instilled into the conjunctival sac of the right eye of one rabbit. The left eye remained untreated and served as a control. Ocular irritation was evaluated by the method of Draize et al. Since irritation cleared by 48 hours and there was no significant irritation observed in this animal, the test was completed on two additional animals.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Remarks:
- opacity
- Basis:
- other: range
- Time point:
- other: 1 - 72 hours
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- iris score
- Basis:
- other: range
- Time point:
- other: 1 - 72 hours
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- other: range
- Time point:
- other: 1 - 72 hours
- Score:
- 0 - 2
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 hours (redness)
- Irritation parameter:
- conjunctivae score
- Remarks:
- chemosis
- Basis:
- other: range
- Time point:
- other: 1 - 72 hours
- Score:
- 0 - 1
- Max. score:
- 4
- Reversibility:
- fully reversible within: 24 hours (chemosis)
- Irritation parameter:
- conjunctivae score
- Remarks:
- discharge
- Basis:
- other: range
- Time point:
- other: 1 - 72 hours
- Score:
- 0 - 2
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 hours (discharge)
- Irritant / corrosive response data:
- One hour after test substance instillation, all three treated eyes exhibited conjunctivitis. The overall incidence and severity of irritation decreased with time. All animals were free of ocular irritation within 72 hours. The ocular scores from individual animals with respect to observation time are presented in Table 1.
- Other effects:
- One animal exhibited soft faeces and ano-genital staining on Days 1 through 4. Body weight loss of 11% of initial weight occurred in this rabbit by study termination. The other two rabbits appeared active and healthy and experienced body weight gain during the study.
Any other information on results incl. tables
Table 1 |
|||||||
Individual Rabbit Ocular Irritation Scores Following Treatment with Test Substance |
|||||||
Rabbit Number |
Cornea |
Iritis |
Conjunctiva |
||||
Opacity |
Area |
Redness |
Chemosis |
Discharge |
|||
1 Hour |
3401 3402 3403 |
0 0 0 |
4 4 4 |
0 0 0 |
2 2 2 |
1 1 1 |
2 1 2 |
24 Hours |
3401 3402 3403 |
0 0 0 |
4 4 4 |
0 0 0 |
1 1 1 |
0 0 0 |
0 1 1 |
48 Hours |
3401 3402 3403 |
0 0 0 |
4 4 4 |
0 0 0 |
0 1 1 |
0 0 0 |
0 0 0 |
72 Hours |
3401 3402 3403 |
0 0 0 |
4 4 4 |
0 0 0 |
0 0 0 |
0 0 0 |
0 0 0 |
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: other: Directive 67/548/EEC; Globally Harmonized System (GHS)
- Conclusions:
- One hour after test substance instillation, all three treated eyes exhibited conjunctivitis. The overall incidence and severity of irritation decreased with time. All animals were free of ocular irritation within 72 hours.
The study and the conclusions which are drawn from it fulfil the quality criteria (validity, reliability, repeatability). - Executive summary:
A primary eye irritation test was conducted with rabbits to determine the potential for the test substance to produce irritation from a single instillation via the ocular route. The study was conducted in a stepwise fashion. Initially, one-tenth of a millilitre of the test substance was instilled into the conjunctival sac of the right eye of one rabbit. The left eye remained untreated and served as a control. Ocular irritation was evaluated by the method of Draize et al. Since irritation cleared by 48 hours and there was no significant irritation observed in this animal, the test was completed on two additional animals. One hour after test substance instillation, all three treated eyes exhibited conjunctivitis. The overall incidence and severity of irritation decreased with time. All animals were free of ocular irritation within 72 hours.
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.