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EC number: 203-127-1 | CAS number: 103-60-6
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 13 August 1979 to 01 October 1979
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: A non-GLP study performed to sound scientific principles with a sufficient level of detail to assess the quality of the submitted data.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 979
- Report date:
- 1979
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Principles of method if other than guideline:
- A 0.5 mL aliquot of the test material was applied to the clipped dorsum of rabbits for 4 hours under a semi-occlusive patch. The irritation reactions were assessed immediately after removal of the patch and after 24, 48 and 72 hours.
- GLP compliance:
- not specified
Test material
- Reference substance name:
- 2-phenoxyethyl isobutyrate
- EC Number:
- 203-127-1
- EC Name:
- 2-phenoxyethyl isobutyrate
- Cas Number:
- 103-60-6
- Molecular formula:
- C12H16O3
- IUPAC Name:
- 2-phenoxyethyl 2-methylpropanoate
- Test material form:
- other: liquid (undefined)
- Details on test material:
- - Name of test material (as cited in study report): phenoxyethyl iso butyrate
- Physical state: Clear liquid.
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Age at study initiation: 9-12 weeks.
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- clipped
- Vehicle:
- unchanged (no vehicle)
- Controls:
- yes
- Amount / concentration applied:
- TEST MATERIAL
- Amount applied: 0.5 mL - Duration of treatment / exposure:
- 4 hours
- Observation period:
- 72 hours
- Number of animals:
- 8
- Details on study design:
- TEST SITE
- Area of exposure: Rabbits were exposed on their dorsum, the specific treatment site were randomised. The whole dorsal surface was clipped 3-4 days before exposure. Only animals in the telogen phase of hair growth were selected.
- Type of wrap if used: Occlusive patches were prepared by attaching a piece of thin flexible polythene (3 cm x 3 cm) to a piece of zinc oxide plaster 9 cm x 2.5 cm. A 2.5 cm square of cotton gauze (8 ply folded in two) was laid on the polythene such that the edges of the pad were attached to the zinc oxide plaster. The test material was applied to the dry patch. The patches were firmly attached to ensure good contact between the skin and the test material. During exposure, the animals were immobilised in a canvas body sleeve.
REMOVAL OF TEST SUBSTANCE
- Washing: The test site was wiped clean of excess test material.
- Time after start of exposure: 4 hours, immediately after patch removal.
REFERENCE STANDARDS
- Diethyl phthalate
- Cyclamen aldehyde
- Geraniol
These standards are perfumery materials that are regularly used as marker controls in skin irritation tests.
All three standards were applied to each of the test rabbits, alongside the test material. Application sites were randomised on the different animals.
SCORING SYSTEM: The skin sites were assessed for irritation immediately after treatment, and at 24, 48 and 72 hours. Each animal was scored blind and the scores for each skin site were not linked to the material tested until the scoring at 72 hours was completed. The sites were scored for erythema, edema, cracking and scaling and any other feature using an 8-point anchored ordinate scale ranging from "a" (very slight) to "h" (severe) see Table 1. At the end of the test the reaction grades for each treatment group were converted to numerical scores which were used to calculate the total irritation score per site.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24 hours
- Score:
- 0.5
- Max. score:
- 12
- Reversibility:
- not fully reversible within: 72 hours
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24 hours
- Score:
- 0.25
- Max. score:
- 12
- Reversibility:
- not fully reversible within: 72 hours
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 48 hours
- Score:
- 0.375
- Max. score:
- 12
- Reversibility:
- not fully reversible within: 72 hours
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 48 hours
- Score:
- 0.375
- Max. score:
- 12
- Reversibility:
- not fully reversible within: 72 hours
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 72 hours
- Score:
- 0.375
- Max. score:
- 12
- Reversibility:
- not fully reversible within: 72 hours
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 72 hours
- Score:
- 0.25
- Max. score:
- 12
- Reversibility:
- not fully reversible within: 72 hours
- Irritant / corrosive response data:
- A single application of test material produced marginal erythema in some animals and marginal edema in a few animals at 24 hours. By 48 hours and 72 hours there was marginal erythema and edema in a few animals. The response was broadly similar to that produced by the control, diethyl phthalate, but considerably less than that produced by the controls, cyclamen aldehyde and geraniol. Total irritation scores of the test material and standards for comparison are given in Table 2, where Table 3 shows the macroscopic findings.
Any other information on results incl. tables
Table 2: Total Irritation Scores
Rabbit No. | Irritation scores | ||||
Diethyl Phthalate | Test Material | Cyclamen Aldehyde | Geraniol | ||
1216 | 0 | 0 | 23 | 32 | |
1217 | 3 | 5 | 31 | 34 | |
1218 | 2 | 3 | 30 | 28 | |
1219 | 4 | 2 | 26 | 26 | |
1220 | 4 | 3 | 35 | 22 | |
1221 | 2 | 0 | 31 | 34 | |
1224 | 2 | 6 | 27 | 38 | |
1244 | 2 | 9 | 41 | 30 | |
Overall irritation score | 19 | 28 | 244 | 244 | |
Mean score per site | 2.38 | 4.0 | 30.5 | 30.5 | |
Mean score per site per day | 0.59 | 1.0 | 7.63 | 7.63 | |
Mean irritation ranking | 1.44 | 1.56 | 3.44 | 3.56 |
Table 3. Macroscopic Findings For Sites Exposed to the Test Material
Rabbit No. | 4 Hours | 24 Hours | 48 Hours | 72 Hours | Totals | Total Score | |||||
Erythema | Edema | Erythema | Edema | Erythema | Edema | Erythema | Edema | Erythema | Edema | ||
1216 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
1217 | 1 | 1 | 1 | 0 | 1 | 0 | 1 | 0 | 4 | 1 | 5 |
1218 | 1 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 2 | 1 | 3 |
1219 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 2 |
1220 | 1 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 2 | 3 |
1221 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
1224 | 0 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 3 | 3 | 6 |
2244 | 1 | 1 | 1 | 1 | 1 | 2 | 1 | 1 | 4 | 5 | 9 |
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Criteria used for interpretation of results: EU
- Conclusions:
- Under the conditions of the test, the test material elicited only very minor reactions in a few of the animals during the course of the study. The test material was concluded to be very slightly irritating. The persistency of this slight irritation continued until termination at 72 hours, no further observations were made.
- Executive summary:
The skin irritation potential of the test material was investigated according to a methodology similar to that of OECD 404. During the study 0.5 mL of the undiluted test material was applied to the clipped dorsum of 8 rabbits for 4 hours under a semi-occlusive patch. The irritation reactions were assessed immediately after removal of the patch and after 24, 48 and 72 hours.
During the course of the study a single application of test material was seen to produce ‘marginal’ erythema and ‘slight’ edema in five out of eight animals at 24 hours. By 48 hours and 72 hours ‘marginal’ erythema and edema was observed in between two and four out of eight animals. The scores assigned in this study are roughly equivalent to a score of 1 according to the Draize scale (1977).
The response was broadly similar to that produced by the control, diethyl phthalate, but considerably less than that produced by the positive controls, cyclamen aldehyde and geraniol.
Under the conditions of the study, the test material was considered to be slightly irritating; however the elicited reaction was below the limits of classification.
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