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EC number: 918-919-9 | CAS number: -
- 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:
- weight of evidence
- Study period:
- 2015
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 015
- Report date:
- 2015
Materials and methods
- Principles of method if other than guideline:
- The protocol for this study is executed according to the ICCVAM Test Method Evaluation Report: Appendix G: ICCVAM Recommended Protocol for Future Studies Using the Hen’s Egg Test-Chorioallantoic Membrane (HET-CAM) Test method, November 2006.
And to Appendix B3 of "ICCVAM Test Method Evaluation Report: Current Validation Status of In Vitro Test Methods Proposed for Identifying Eye Injury Hazard Potential of Chemicals and Products", NIH Publication No. 10-7553, September 2010.
The Hen´s Egg Test on the Chorioallantoic Membrane (HET-CAM) is a test method which implies the use of a complete tissue constituted of blood vessels and proteins that is capable of responding to chemical injury with an inflammatory process similar to the one occurring in the conjunctival tissue of the eye.
- Short description of test conditions: The test substance is applied directly to the chorioallantoic membrane (CAM) of fertilized chicken eggs
- Parameters analysed / observed: acute effects on haemorrhage, lysis of blood vessels and coagulation - GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- 2-({[4-({bis[4-({[2-(prop-2-enoyloxy)ethoxy]carbonyl}amino)phenoxy](sulfanylidene)-λ⁵-phosphanyl}oxy)phenyl]carbamoyl}oxy)ethyl prop-2-enoate
- EC Number:
- 918-919-9
- Cas Number:
- 1072454-85-3
- Molecular formula:
- C36H36N3O15PS
- IUPAC Name:
- 2-({[4-({bis[4-({[2-(prop-2-enoyloxy)ethoxy]carbonyl}amino)phenoxy](sulfanylidene)-λ⁵-phosphanyl}oxy)phenyl]carbamoyl}oxy)ethyl prop-2-enoate
- Reference substance name:
- Ethyl acetate
- EC Number:
- 205-500-4
- EC Name:
- Ethyl acetate
- Cas Number:
- 141-78-6
- Molecular formula:
- C4H8O2
- IUPAC Name:
- ethyl ethanoate
- Test material form:
- liquid
Constituent 1
additive 1
Test animals / tissue source
- Details on test animals or tissues and environmental conditions:
- The test system used for this study is the fertile Lohmann Brown hen egg which is incubated for 8 days before test item application.
SOURCE OF FERTILIZED CHICKEN EGGS
- Source: Brinkschulte Josef GmbH & Co.KG, 48308 Senden
- Number of eggs: 4
- Treatment conditions of eggs prior initiating testing: day 1-7: an incubator with an automatic rotating device (e.g. Ehret GmbH), optimum temperature : 37.5 °C, relative humidity 63 %. day 8: with the large end upward and not rotated for ensuring accessibility to the Chorioallantoic membrane (CAM) region
- Time interval prior to initiating testing: 8 days
- indication of any existing defects or lesions in eggs: After 7 days of incubation, all eggs were candled in order to discard those that were defect and to mark the air bubble.
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- yes, concurrent positive control
- yes, concurrent negative control
- other: The test material is a solution in ethyl acetate. Ethyl acetate was tested independently in parallel to distinguish potential toxic effects of the test item from the effects of the solvent.
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 300 µL per egg - Duration of treatment / exposure:
- 300 seconds (i.e. 5 min) after substance application
- Duration of post- treatment incubation (in vitro):
- not applicable
- Number of animals or in vitro replicates:
- 4 eggs per group (negative control, positive control, test substance, solvent)
- Details on study design:
- METHODS:
At day 8 of incubation the sections marked for the air bubble were sawed out of the shell. The inner membrane was moistened with NaCl 0.9 % and carefully removed with forceps. Only eggs with normally developed embryos and blood vessel systems are used for testing.
Undiluted test item is applied directly onto the Chorioallantoic membrane (CAM) of each egg in a volume of 300 μL.
4 eggs each were used for the test item, negative and positive controls.
Observations of effects to the blood vessels, albumen or to the embryo over a period of 300 seconds after substance application are determined for each single egg. The time to the appearance of each of the observations mentioned above has been monitored and recorded. If no effect appeared during the observation period of 300 seconds (observation = 0) the result was assigned as negative for the related endpoint, and the factor set to 0 for this endpoint when calculating the Irritation Score (IS).
OBSERVATIONS:
0= no effect
1 = vasodilatation, slight haemorrhage (H)
2 = vessel lysis, strong haemorrhage (L)
3 = blood-coagulation, albumen -coagulation (C)
The time to the appearance of each of the observations mentioned above has been monitored and recorded. If no effect appeared during the observation period of 300 seconds (observation = 0) the result was assigned as negative for the related endpoint, and the factor set to 0 for this endpoint when calculating the IS.
IRRITATION SCORE:
Following formula was used to generate an irritation score (IS):
IS = 5 x (301-sec H)/300 + 7 x (301- sec L)/300 + 9 x (301- sec C)/300
H= observed start in seconds of haemorrhage reactions
L= observed start in seconds of vessel lysis, strong haemorrhage
C= observed start in seconds of blood-coagulation, albumen-coagulation
Assessment of Irritation Scores (IS) according to Luepke, N.P., Fd. Chem. Toxic 23, 287-291, 1985:
Score Assessment
0 - 0.9 no irritation
1 - 4.9 slight irritation
5 - 8.9 moderate irritation
9 - 21 strong irritation
A test substance is considered to cause severe eye irritation when the Irritation Score is equal to or above 9.
Results and discussion
In vitro
Results
- Irritation parameter:
- other: Irritation Score (IS)
- Run / experiment:
- mean of 4 eggs
- Value:
- 11
- Vehicle controls validity:
- not applicable
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Remarks on result:
- other: the solvent ethyl acetate was tested in parallel and showed an Irritation Score of 13
In vivo
- Irritant / corrosive response data:
- The test item was identified as "strong irritant" to the chorioallantoic membrane (irritation score (IS) = 11) under the conditions of this assay. The solvent ethyl acetate was even stronger irritating with an IS of 13.
Any other information on results incl. tables
Table 1: Summary of results from HET-CAM test with the test item
Compound |
Irritation Score (IS) |
Assessment |
Negative control NaCl 0.9 % |
0 |
non irritant |
Positive control SDS 1 % |
12 |
strong irritant |
Test item |
11 |
strong irritant |
solvent ethyl acetate | 13 | strong irritant |
Applicant's summary and conclusion
- Interpretation of results:
- other: positive
- Executive summary:
The test item was identified as 'strong irritant' to the chorioallantoic membrane (irritation score (IS) = 11 of maximal 21) to fertilized hen's eggs under the conditions of the HET-CAM test (Hen's Egg Test - Chorioallantoic Membrane) according to a protocol recommended by ICCVAM. The test material is a solution in ethyl acetate. Ethyl acetate was tested independently in parallel to distinguish potential toxic effects of the test item from the effects of the solvent. Ethyl acetate showed stronger effects than the test item with an IS of 13.
The results of the positive (SDS 1 % in physiologic saline) and negative (physiologic saline solution) controls confirmed the validity of the test system.
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