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EC number: 239-701-3 | CAS number: 15625-89-5
- 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:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: well conducted and documented study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 978
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- other: In general the techniques of tests as published by the FDA af the United States (Fed. Reg. 28 (119), 5582, 1963) and Draize and Kelley (Drug Gosmet. Industr. 71 (1952) 36) are followed.
- Principles of method if other than guideline:
- Principles according to Draize
- GLP compliance:
- no
Test material
- Reference substance name:
- 2-ethyl-2-[[(1-oxoallyl)oxy]methyl]-1,3-propanediyl diacrylate
- EC Number:
- 239-701-3
- EC Name:
- 2-ethyl-2-[[(1-oxoallyl)oxy]methyl]-1,3-propanediyl diacrylate
- Cas Number:
- 15625-89-5
- Molecular formula:
- C15H20O6
- IUPAC Name:
- 2,2-bis(prop-2-enoyloxymethyl)butyl prop-2-enoate
- Details on test material:
- - Name of test material (as cited in study report): trimethylolpropane triacrylate
- Physical state: slightly yellow, viscous liquid
- Analytical purity: > 78%
- Impurities (identity and concentrations): three of four impurities were tentatively identified as thylolpropane diacrylate, trimethylolpropane triacrylate-trimethylol-propane monoacrylate adduct, and trimethylolpropane triacrylate-trimethylol-propane diacrylate adduct
- Periodic reanalysis was performed at least every 6 months, no degeneration was detected
- Lot/batch No.: 08409HI (Aldrich Chemical Company, Milwaukee, WI)
- Stability under test conditions: stability was confirmed for up to 35 days at room temperature (sealed amber glass containers) and for up to 3h in simulated animal room conditions (not sealed)
- Storage condition of test material: room temperature protected from light in amber glass containers sealed with Teflon-lined lids.
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- Ihe animais are caged individually and receive no hay or other extranous material that might enter the eyes
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: second eye serves as control
- Amount / concentration applied:
- - undiluted
- 100µL - Duration of treatment / exposure:
- Treatment: After installtion the upper and lower eye lid are then carefully clased and subsequently held together for at least one second before releasing, to prevent loss of material. The other eye remaining untreated, serves as a control.The eyes are not washed following instillation and the animals
are released immediately. - Observation period (in vivo):
- The eyes are examined at one hour, 24, 48, 72 hours and 7 days after instillation of the test material.
- Number of animals or in vitro replicates:
- 2
- Details on study design:
- Ocular reactions are judged using the scoring seale as published by Draize and Kelley (Drug. Gosmet. Industr. 71 (1952) 36)
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Remarks:
- opacity
- Basis:
- animal #1
- Time point:
- 24 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: highest value of 3 after 7 days
- Irritation parameter:
- cornea opacity score
- Remarks:
- opacity
- Basis:
- animal #1
- Time point:
- 48 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: highest value of 3 after 7 days
- Irritation parameter:
- cornea opacity score
- Remarks:
- opacity
- Basis:
- animal #1
- Time point:
- 72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: highest value of 3 after 7 days
- Irritation parameter:
- cornea opacity score
- Remarks:
- opacity
- Basis:
- animal #2
- Time point:
- 24 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- cornea opacity score
- Remarks:
- opacity
- Basis:
- animal #2
- Time point:
- 48 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- cornea opacity score
- Remarks:
- opacity
- Basis:
- animal #2
- Time point:
- 72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Time point:
- 24 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Time point:
- 48 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Time point:
- 72 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- iris score
- Basis:
- animal #2
- Time point:
- 24 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- iris score
- Basis:
- animal #2
- Time point:
- 48 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- iris score
- Basis:
- animal #2
- Time point:
- 72 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #1
- Time point:
- 24 h
- Score:
- 3
- Max. score:
- 3
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #1
- Time point:
- 48 h
- Score:
- 3
- Max. score:
- 3
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #1
- Time point:
- 72 h
- Score:
- 3
- Max. score:
- 3
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #2
- Time point:
- 24 h
- Score:
- 2
- Max. score:
- 3
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #2
- Time point:
- 48 h
- Score:
- 2
- Max. score:
- 3
- Reversibility:
- not fully reversible within: 7 days
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #2
- Time point:
- 72 h
- Score:
- 2
- Max. score:
- 3
- Reversibility:
- not fully reversible within: 7 days
- Irritant / corrosive response data:
- no corrosive effects reported
Applicant's summary and conclusion
- Interpretation of results:
- other:
- Conclusions:
- From the present results it can be coneluded that the compound na. 77/767 is moderately irritating to the eye.
- Executive summary:
A eye irritation study according to the general techniques as published by the FDA of the(Fed. Reg. 28 (119), 5582, 1963) and Draize and Kelley (Drug Gasmet. Industr. 71 (1952) 36) was conducted to assess the eye irritation potential of TMPTA.
Therefore two New Zealand White albino rabbits received 100 milligrams of the test substance. No washout followed the instillation and the eyes are examined at one hour, 24, 48, 72 hours and 7 days. Ocular reactions are judged using the scoring scale as published by Draize and Kelley (Drug. Gosmet. Industr. 71 (1952) 36)
During the first day after instillation the eyes showed slight corneal damage, slight iritis and moderate to severe lesions of the conjunctivae.
In the course of the seven-day observation period the degree of corneal
damage increased. After seven days the following ocular lesions were observed: moderate or moderate-severe corneal opacity, slight iritis and moderate conjunctivitis.
Results are summarized as follows: eye irritation score (two animais used): 44
The author concluded that, according to the classification used, the test material is moderately irritating to the eye.
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