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EC number: 256-360-6 | CAS number: 48145-04-6
- 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
Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: basic information given
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 982
- Report date:
- 1982
Materials and methods
- Principles of method if other than guideline:
- according to Smyth, H.F. et al.: Am. Ind. Hyg. Ass. J. 23, 95-107 (1962)
- GLP compliance:
- no
- Test type:
- other: inhalation hazard test
Test material
- Reference substance name:
- 2-phenoxyethyl acrylate
- EC Number:
- 256-360-6
- EC Name:
- 2-phenoxyethyl acrylate
- Cas Number:
- 48145-04-6
- Molecular formula:
- C11H12O3
- IUPAC Name:
- 2-phenoxyethyl prop-2-enoate
- Details on test material:
- Name of the test substance used in the study report: 2-Phenoxyethylacrylat
Purity: ca. 70%
Remaining acrylic acid < 1%
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Acclimatization period: at least 5 days
Age at study start: 7 - 10 weeks
Body weight at study start: 180 - 250 g
Animal identification: toe amputation
3 animals per cage (wire mesh cages; type Becker D III)
Housing conditions: room temperature 22 +/- 2°C, relative humidity 55 +/- 5%, day/night rhythm 12 h/12 h
The animals were offered a standardized animal laboratory diet ad libitum; drinking water: daily 250 ml/cage
Administration / exposure
- Route of administration:
- inhalation
- Details on inhalation exposure:
- The product was filled in a glass bottle to a height of 5 cm (fritted glas flask, pore size 90 - 150 um, diameter 30 mm), and the net weight was determined.
A stream of 200 l/h compressed air was supplied to the fritted glass flask containing the product, which had been placed in a water bath maintained at 20 ± 1°C by a thermostat. The mixture of air and test substance generated in this way was passed through a glass distributor to 6 glass tubes in which 3 male and 3 female animals had been placed. The emerging mixtures of test substance and air were exhausted.
After 30 minutes, the fritted glass flask was replaced by a new one filled with fresh test substance as described above. This receiver was then used for the whole remaining time of the test.
The test substance consumed was determined by reweighing the fritted glass flasks. The exposure time was 7 hours. The intention was to determine the exposure time which was survived by all the animals including a post-exposure observation period lasting 14 days in 2 experiments. - Duration of exposure:
- 7 h
- Concentrations:
- not given
- No. of animals per sex per dose:
- 6
- Details on study design:
- Clinical signs or lethality of the animals were recorded daily.
The animals that died or those sacrificed with carbon dioxide at the end of the post-exposure observation period were subjected to a gross-pathological examination.
Results and discussion
- Mortality:
- None
- Clinical signs:
- other: During exposure: restlessness, snout wiping After exposure: no abnormalities detected
- Gross pathology:
- Organs: nothing abnormal detected
Applicant's summary and conclusion
- Conclusions:
- No clear conclusion from this study can be made as exposure concentration was not given.
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.
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