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EC number: 469-300-0 | CAS number: 63675-73-0
- 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:
- Jun 2006 to Feb 2007
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 007
- Report date:
- 2007
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- GLP compliance:
- yes
Test material
- Reference substance name:
- -
- EC Number:
- 469-300-0
- EC Name:
- -
- Cas Number:
- 63675-73-0
- Molecular formula:
- Hill Empirical Formula: C16H16O3S CAS Empirical Formula: C16H16O3S
- IUPAC Name:
- 1-(4-methoxyphenyl)-2-[(3-methoxyphenyl)sulfanyl]ethan-1-one
- Test material form:
- solid: particulate/powder
- Details on test material:
- Lot no: 151105Purity - 101.39%
Constituent 1
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- At approximately 24-hour intervals after the start of the incubation period, volumes of test media were removed from each incubated test vessel, and transferred to individually identified cell counting vials. The content of each vial was diluted to a 10 mL final volume with an electrolyte solution. The number of alga cells in duplicate 0.5 mL volumes, drawn into the counter (under vacuum) from each vial, was then determined using a particle counter (22 Coulter Counter®). These values were then used to establish cell densities (cells/ml) for each of the incubated test vessels used in the test.
Test solutions
- Vehicle:
- yes
- Remarks:
- Acetone
- Details on test solutions:
- The dilution media used was algae nutrient medium (EC media). The definitive test was conducted at nominal Beta Ketosulfide concentrations of control, 0.088, 0.159, 0.287, 0.516, 0.929, 1.67 and 3.01 mg/L. The selected concentrations were based on the results of the range-finding test and the practical solubility limit for the test substance.A test medium at a nominal concentration of 100 mg!L, was prepared by weighing 199.98 mg of Beta Kctosulfide into a glass vessel and adding 200 µL of acetone. The vessel contents were then rinsed into a 2-litre volumetric flask and made up to volume with EC medium. The flask contents was then treated with ultrasound for 30 minutes, stirred for 1 hour in the dark and filtered through a 0.45µm pore sized filter. The remaining test media then were prepared by serially diluting the nominal 100 mg!L test medium. Additional aliquots of acetone were added to each test media preparation as it was prepared, to ensure that a solvent loading of 0.1 mUL was achieved in the solvent control a nd in all treatments.The solvent control treatment was prepared by adding 100 µL of acetone to a 1000 mL volumetric flask and making up to volume with EC medium. The control treatment was prepared by adding EC medium only to the test vessels.
Test organisms
- Test organisms (species):
- Raphidocelis subcapitata (previous names: Pseudokirchneriella subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- The test organism, Pseudokirchneriel/a subcapitata (Strain 278/4) was obtained from the CCAP (Culture Collection of Algae and Protozoa) and is a representative species of the freshwater aquatic phytoplankton. This species is recommended for testing in accordance with the OECD regulatory guidelines. The P. subcapitata culture used was derived from the CCAP, SAMS Research Services Ltd., Oban, UK.Prior to testing, duplicate starter cultures were prepared and incubated under test conditions. A start ing alga cell density of 1 x 10^4 algacells/mL was achieved.
Study design
- Test type:
- semi-static
- Water media type:
- other: Reverse osmosis water
- Limit test:
- no
- Total exposure duration:
- 72 h
- Post exposure observation period:
- At 72 hours, measured concentrations of Beta Ketosulfide had declined significantly, resulting in overall mean measured concentrations outside 80-120% of the nominal concentrations. Therefore, the toxicity values have been reported in terms of the overal! (geometric) mean measured test conc entrations. The limit of detection for the analytical method was 0.008 mg/L.
Test conditions
- Hardness:
- Not measured
- Test temperature:
- 23.3-24.3C
- pH:
- 7.7-7.9 initially. Increased to 9.9 after 72 hrs with algal cells
- Dissolved oxygen:
- Not measured
- Salinity:
- Not measured
- Conductivity:
- Not measured
- Nominal and measured concentrations:
- The overall mean (geometric) measured concentrations of Beta Ketosulfide at the respective nominal concentrations of 0.088, 0.159, 0.287, 0.516, 0.929, 1.67 and 3.01 mg!L were 0.0408, 0.0893, 0.155, 0.290, 0.747, l.57 and 2.76 mg/L, respectively. These values correspond to 46, 56, 54, 56, 80, 94 and 92 % of the nominal concentrations, respectively.
- Details on test conditions:
- The dilution media used was algae nutrient medium (EC media). The definitive test was conducted at nominal Beta Ketosulfide concentrations of control, 0.088, 0.159, 0.287, 0.516, 0.929, 1.67 and 3.01 mg/L. The selected concentrations were based on the resu lts of the range-finding test and the practical solubility limit for the test substance.A test medium at a nominal concentration of 100 mg!L, was prepared by weighing 199.98 mg of Beta Kctosulfide into a glass vessel and adding 200 µL of acetone. The vessel contents were then rinsed into a 2-litre volumetric flask and made up to volume with EC medium. The flask contents was then treated with ultrasound for 30 minutes, stirred for 1 hour in the dark and filtered through a 0.45µm pore sized filter. The remaining test media then were prepared by serially diluting the nominal 100 mg!L test medium. Additional aliquots of acetone were added to each test media preparation as it was prepared, to ensure that a solvent loading of 0.1 mUL was achieved in the solvent control and in all treatments.The solvent control treatment was prepared by adding 100 µL of acetone to a 1000 mL volumetric flask and making up to volume with EC medium. The control treatment was prepared by adding EC medium only to the test vessels.
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- ca. 0.615 mg/L
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- ca. 1.21 mg/L
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- ca. 0.29 mg/L
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- ca. 0.29 mg/L
- Basis for effect:
- biomass
- Details on results:
- Toxicity ValuesStatistical comparison of growth (area under the growth curve and specific growth rate data) in the c ontrol and solvent control treatments, revealed no significant differences between the two treatments. Therefore, the ErC5o and EbC.so toxicity values have been detennined by comparison of treatments with combined (pooled) control data.Based on the overall mean measured concentrations of Beta Ketosulfide, the 0 - 72 hour EbC50 and Er C50 toxicity values with corresponding NOEC values are presented in the table below (see any other information on results incl. tables).
Any other information on results incl. tables
follow on from "Details on results" section
CI = 95% confidence interval
Parameter | Toxicity Values (EC50 and NOEC)
Overall mean measured Beta Ketosulfide Concentration (mg/l) |
0 -72 hour Er C50
NOEC | 1.21 (CI = 1.09 -1.34)
0.290 |
0 -72 hour Eb C50
NOEC | 0.615 (CI =0.363 -1.04)
0.290 |
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- The acute toxicity of Beta Ketosulfide, on the growth of the unicellular green algae, Pseudokirchner iella subcapitata was determined during a 72 hour growth inhibition toxicity test.The test was conducted in accordance with the known requirements of OECD Chemical Testing Guideline No. 201 Algae, Growth Inhibition tests (adopted 7 June 1984). In terms of the overall mean measureed concentrations, based on the growth rate toxicity values, Beta Ketosulfide exposure to P. subcapitata was considered to be toxic (where toxicity values > 1mg/ L and <= 10 mg/L) and may cause long term adverse effects in the aquatic environment. For the area under the growth curve (0-72 hour Eb C50), Beta ketosulfide would be consided to be very toxic , as the toxicity value was <= 1mg/L. The toxicity values have already been presented above.
- Executive summary:
This test was conducted in accordance with the known requirements of OECD Chemical Testing
Guideline No. 201 Algae, Growth Inhibition Test (adopted 7 June 1984)
The ErC50 (0 -72 hrs) = 1.21, NOEC = 0.290
The EbC50 (0 -72 hrs) = 0.615, NOEC = 0.290
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