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Diss Factsheets
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EC number: - | 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
Toxicity to aquatic algae and cyanobacteria
Administrative data
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2020-12-07 to 2021-03-15
- Reliability:
- 1 (reliable without restriction)
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 021
- Report date:
- 2021
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- Reaction mass of 2-(3a,4,5,6,7,7a-hexahydro-1H-4,7-methanoinden-5-yloxy)ethyl acrylate and 2-(3a,4,5,6,7,7a-hexahydro-1H-4,7-methanoinden-6-yloxy)ethyl acrylate
- Molecular formula:
- C15 H20 O3
- IUPAC Name:
- Reaction mass of 2-(3a,4,5,6,7,7a-hexahydro-1H-4,7-methanoinden-5-yloxy)ethyl acrylate and 2-(3a,4,5,6,7,7a-hexahydro-1H-4,7-methanoinden-6-yloxy)ethyl acrylate
- Test material form:
- liquid
- Details on test material:
- - Name: 2-Propenoic acid,2-[[3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-5(or 6)-yl]oxy]ethyl ester
- CAS No.: 68169-12-0 (outside EU)
- EC Name: Reaction mass of 2-(3a,4,5,6,7,7a-hexahydro-1H-4,7-methanoinden-5-yloxy)ethyl acrylate and 2-(3a,4,5,6,7,7ahexahydro-1H-4,7-methanoinden-6-yloxy)ethyl acrylate
- EC Number: 951-956-9
- Batch No.: OX8J0799
- Molecular Weight: 248.32 g/mol
- Physical State: liquid
- Colour: clear
- Active Components: 98.52% active components (different isomers), 1.48% 2-Cyclopenta-1,3-dienyloxyethan-1-ol
- Purity: 98.52%
- Expiry Date: 17 September 2023
- Storage Conditions: room temperature
- Safety Precautions: The routine hygienic procedures were sufficient to assure personnel health and safety.
Constituent 1
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- Separate replicates for the test item analysis after 0 hours and 72 hours were prepared in the original test vessels with algae at the start of the exposure. The replicates for test end were incubated under test conditions until analysis.
Test solutions
- Vehicle:
- no
- Details on test solutions:
- Seven water accommodated fractions (WAF) were prepared with nominal loading rates of the test item in the range of 0.0110 to 11.0 mg/L set up in a geometric series with a factor of √10. Three water accommodated fraction with a nominal loading of 11.0, 3.48 and 1.10 mg/L were prepared separately. For the loading rates, an appropriate amount of the test item was pipetted onto the surface of the dilution water in a glass bottle. For this purpose, the density was taken into account. These dispersions were shaken for at least 24 hours with 20 rpm at room temperature. After a separation phase of 1 hour, the aqueous phase or WAF was removed by siphoning (from the approximate center of the glass flask). The WAFs were checked via laser beam (Tyndall effect) for undissolved test item (formation of an emulsion). The Tyndall effect was negative. The resulting water accommodated fractions (WAF) were used in the test. Appropriate volumes of the WAF 1.10 mg/L were diluted with dilution water to achieve the other 4 loading levels for testing: 0.0110 – 0.0348 – 0.110 – 0.348 mg/L.
Test organisms
- Test organisms (species):
- Raphidocelis subcapitata (previous names: Pseudokirchneriella subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- Cultivation at test facility: Fresh stocks are prepared every month on Z-Agar. Light intensity amounts 2567 – 5130 lux for 24 hours per day.
Culture medium: Nutrient medium Z according to LÜTTGE et al. (1994)
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
Test conditions
- Test temperature:
- 22.5 - 23.5
- pH:
- 8.04 - 9.10
- Nominal and measured concentrations:
- nominal: 11, 3.48, 1.1, 0.348, 0.11, 0.0348, 0.011 mg/L
measured: 10.1, 2.4, 0.406, 0.109, 0.0333, 0.00998, 0.00363 mg/L - Reference substance (positive control):
- yes
Results and discussion
Effect concentrationsopen allclose all
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EL10
- Effect conc.:
- 0.011 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Remarks on result:
- other: water accommodated fractions (WAF)
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EL50
- Effect conc.:
- 0.807 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Remarks on result:
- other: water accommodated fractions (WAF)
- Details on results:
- All effect values given are based on the nominal loading rates of the test item.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- Based on the nominal loading rates, the 72 hours-EL50 was 0.807 mg/L, and the EC10 was 0.0112 mg/L.
- Executive summary:
The aim of the study was the determination of the effects on growth rate and yield over a period of 72 hours.
The study was conducted under static conditions with an initial cell density of 6352 cells/mL. Seven water accommodated fractions (WAF) were prepared with nominal loading rates of the test item in the range of 0.0110 to 11.0 mg/L set up in a geometric series with a factor of √10. Three water accommodated fraction with a nominal loading of 11.0, 3.48 and 1.10 mg/L were prepared separately. Appropriate volumes of the WAF 1.10 mg/L were diluted with dilution water to achieve the other 4 loading levels for testing: 0.0110 – 0.0348 - 0.110 – 0.348 mg/L.
Three replicates were tested for each test item loading and six replicates for the control. The environmental conditions were within the acceptable limits.All loading rates of the test item and the control were analytically determined in fresh media (0 hours) and at the end of the exposure interval (72 hours) via GC-MS. At the start of the exposure the measured concentrations were in the range of 0.00555 to 10.7 mg/L. At the end of exposure after 72 hours, the measured concentrations were in the range of 54 to 95% of the initially measured concentrations of the test item.
Based on the nominal loading rates, the 72 hours-EL50 was 0.807 mg/L, and the EC10 was 0.0112 mg/L.
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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