Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 218-645-3 | CAS number: 2210-79-9
- 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
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to the O.E.C.D. test guideline 201 with GLP compliance.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 012
- Report date:
- 2012
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Deviations:
- yes
- Remarks:
- Nominal concentrations only.
- GLP compliance:
- yes
Test material
- Reference substance name:
- 2,3-epoxypropyl o-tolyl ether
- EC Number:
- 218-645-3
- EC Name:
- 2,3-epoxypropyl o-tolyl ether
- Cas Number:
- 2210-79-9
- Molecular formula:
- C10H12O2
- IUPAC Name:
- oxirane
- Reference substance name:
- Oxirane, 2-[(2-methylphenoxy)methyl]-
- IUPAC Name:
- Oxirane, 2-[(2-methylphenoxy)methyl]-
- Details on test material:
- As per IUCLID Sections 1.1. 1.2. and 4.1.
Constituent 1
Constituent 2
Sampling and analysis
- Analytical monitoring:
- no
Test solutions
- Vehicle:
- no
- Details on test solutions:
- Test substance treatment solutions were prepared by by adding the required nominal amount of test substance in stock culture medium (Woods Hole) and mixing.
Test organisms
- Test organisms (species):
- Raphidocelis subcapitata (previous names: Pseudokirchneriella subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- The green algae Selenastrum capricornutum was maintained by Stillmeadow, Inc. Mass culture initiated 3-7 ±1 days prior to dosing and were used on-study at a density of 50,000 cells/mL. The algal cultures were maintained in Algal stock culture medium (Woods Hole) with EDTA up to 0.300 mg/L in 250-mL sterile Erlenmeyer flasks with stoppers and aeration tubing. The test containers received constant aeration. The temperature was maintained at 24 ±2°C with continuous lighting (400 ±40 ft. c.).
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Post exposure observation period:
- None
Test conditions
- Hardness:
- No data
- Test temperature:
- 24ºC
- pH:
- 7.4-8.9 treminal
- Dissolved oxygen:
- no data
- Salinity:
- Freshwater
- Nominal and measured concentrations:
- 1.25, 2.5, 5, 10 and 20 mg/L nominal.
- Details on test conditions:
- The five concentrations of the test substance were used. The test cultures (50,000 cells/mL) were divided into 250-mL flasks containing the appropriate concentration of test substance (three flasks per test concentration and six flasks for the control). A positive control group consisted of three flasks treated with 10 mg/L zinc chloride. The flasks were set on a shaker table for constant agitation at approximately 100 cycles/minute. At 24, 48 and 72 hours following dosing, observations of inhibition were made for each test container by measuring the mean cell density with a hemacytometer. The temperature was recorded daily and the pH of each container was recorded at study termination.
- Reference substance (positive control):
- yes
- Remarks:
- 10 mg/L zinc chloride
Results and discussion
Effect concentrations
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- ca. 5.1 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- cell number
- Remarks on result:
- other: 95% confidence Limits = 0.0 - 9.85 mg/L nominal
- Details on results:
- At 10 mg/L test substance after 72 hr the relative percent cell growth inhibition was 35.9%. Complete cell growth inhibition was observed at 20 mg/L of test substance at 72 hr.
- Results with reference substance (positive control):
- The positve control zinc chloride at 10 mg/L caused complete (100%) cell growth inhibiton at 72 hr relative to the untreated control cultures.
- Reported statistics and error estimates:
- The EC50 95% Confidence Limits were 0.0 - 9.85 mg/L (nominal).
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- The EC50 value for the test substance in this study of 5.1 mg/L demonstrates that it is toxic to algae under the conditions of the study.
- Executive summary:
The test substance, 2,3 -epoxypropyl o-tolyl ether, was accesed for toxicity to green algae in a GLP, O.E.C.D. test gudeline 201 study.The EC50 value for the test substance in this study of 5.1 mg/L demonstrates that it is toxic to algae under the conditions of the study.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.