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EC number: 218-620-7 | CAS number: 2206-94-2
- 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 vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to the appropriate OECD test guideline, and in compliance with GLP. There was an uncritical deviation from the guidelines.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 015
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 437 (Bovine Corneal Opacity and Permeability Test Method for Identifying Ocular Corrosives and Severe Irritants)
- Deviations:
- yes
- Remarks:
- The measurement of the opacity was performed with a photometer (570 nm) instead of an opacitometer. This can be seen as uncritical, because the opacity can be calculated from the absorbances.
- Qualifier:
- according to guideline
- Guideline:
- EU method B.47 (Bovine corneal opacity and permeability test method for identifying ocular corrosives and severe irritants)
- Deviations:
- yes
- Remarks:
- The measurement of the opacity was performed with a photometer (570 nm) instead of an opacitometer. This can be seen as uncritical, because the opacity can be calculated from the absorbances.
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- (Date of inspection: 2014-10-13/14, Date of signature: 2015-04-08)
Test material
- Reference substance name:
- α-methylenebenzyl acetate
- EC Number:
- 218-620-7
- EC Name:
- α-methylenebenzyl acetate
- Cas Number:
- 2206-94-2
- Molecular formula:
- C10H10O2
- IUPAC Name:
- 1-phenylethenyl acetate
- Test material form:
- other: liquid
Constituent 1
Test animals / tissue source
- Species:
- other: Bovine
- Strain:
- not specified
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: Three corneas were used for positive and negative controls
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 750 μl
CONTROLS
- Positive control substance: Dimethylformamide, DMF, CAS-No. 68-12-2, undiluted.
- Negative control substance: Sodium chloride solution: 0.9% NaCl (CAS-No. 7647-14-5), dissolved in demin. water. - Duration of treatment / exposure:
- 10 minutes incubation at 32 ± 1°C
- Observation period (in vivo):
- The corneas were stored for additional 2 h at 32 ± 1 °C (post-incubation).
Optical density measured after a further 90 ± 5 min at 32 ± 1 °C incubation in medium with fluoroscein - Number of animals or in vitro replicates:
- For each treatment group (negative control solution, test item and positive control), three replicates were used.
Results and discussion
In vivo
Results
- Irritation parameter:
- other: In vitro irritation score
- Basis:
- other: opacity and permeability
- Score:
- 0.02
- Remarks on result:
- other: negative control score: 0.21; positive control score: 105.86; not irritating
Any other information on results incl. tables
For each treatment group (negative control solution, test item and positive control), three replicates were measured.
The absorbance (570 nm) and opacity values which were measured before and after exposure are given in the following table:
Absorbance and Opacity Values Negative Control
Parameter |
Negative Control |
||
Absorbance before exposure |
0.1888 |
0.1907 |
0.1792 |
Absorbance after exposure |
0.2395 |
0.2033 |
0.2148 |
Opacity before exposure |
1.5445 |
1.5513 |
1.5108 |
Opacity after exposure |
1.7358 |
1.5970 |
1.6398 |
Opacity Difference |
0.1913 |
0.0457 |
0.1291 |
Mean opacity difference of the negative control is 0.1220.
Absorbance and Opacity Values Test Item and Positive Control
Parameter |
Test Item |
Positive Control |
||||
Absorbance before exposure |
0.3106 |
0.1407 |
0.2123 |
0.1425 |
0.1296 |
0.1766 |
Absorbance after exposure |
0.3383 |
0.1515 |
0.3066 |
1.9991 |
1.8398 |
1.9957 |
Opacity before exposure |
2.0446 |
1.3826 |
1.6304 |
1.3884 |
1.3477 |
1.5018 |
Opacity |
2.1792 |
1.4174 |
2.0258 |
99.7930 |
69.1512 |
99.0148 |
Opacity |
0.1347 |
0.0348 |
0.3954 |
98.4046 |
67.8035 |
97.5130 |
For the permeability measurement, three replicates for each treatment group were measured. The optical density values at 490 nm are given in the following table:
Optical density at 490 nm
Replicate |
Negative Control |
Test ItemAlpha Methylenebenzyl Acetate |
Positive Control |
||||||
Measured values |
-0.0004 |
0.0007 |
0.0031 |
0.0003 |
-0.0004 |
0.0016 |
0.1997 |
0.2629 |
0.2637 |
*Corrected values |
-0.0020 |
0.0035 |
0.0155 |
0.0015 |
-0.0020 |
0.0080 |
0.9985 |
1.3145 |
1.3185 |
Mean |
0.0057 |
-- |
*Note: In order to correct the path length, a factor of 5 was taken into account when calculating the IVIS (see previous chapter).
IVIS Values
IVIS was calculated using the values in tables 9.1-a, 9.1-b and 9.1-c and the equation stated in chapter8.3.
Example:
IVIS (Test Item Alpha Methylenebenzyl Acetate, Repl. 1) =
(0.1347 – 0.1220) + [15 * (0.0015 – 0.0057)] = -0.05
The calculated IVIS for each replicate and the corresponding means are presented in the following table:
IVIS
Test Group |
IVIS |
Mean IVIS |
Standard Deviation of IVIS |
Relative Standard Deviation of IVIS |
Negative Control |
0.16 |
0.21 |
0.138 |
66.4% |
0.10 |
||||
0.36 |
||||
Test Item |
-0.05 |
0.02 |
0.262 |
1456.2% |
-0.20 |
||||
0.31 |
||||
Positive Control |
113.18 |
105.86 |
16.178 |
15.3 % |
87.31 |
||||
117.08 |
Note: the high relative standard deviations of the IVIS of test item and negative control are due to mathematical reasons, as the respective means are very small.
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The eye irritancy potential of α-methylenebenzyl acetate has been investigated in a valid in vitro bovine corneal opacity and permeability assay conducted in accordance with OECD 437 and in compliance with GLP. The following mean in vitro irritation score was calculated: 0.02. The in vitro irritation score obtained with the positive control fell within the two standard deviations of the current historical mean and therefore this assay is considered to be valid. It is concluded that the test substance is not irritating to the eye.
- Executive summary:
α-Methylenebenzyl acetate has been tested for eye irritation investigated in a valid in vitro bovine corneal opacity and permeability assay conducted in accordance with OECD 437 and in compliance with GLP. The test item did not meet the criteria for classification.
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