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EC number: 213-860-9 | CAS number: 1038-28-4
- 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

Short-term toxicity to fish
Administrative data
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Aug - Sept 1994
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: According to OECD guideline under GLP
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 995
- Report date:
- 1995
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Principles of method if other than guideline:
- Not relevant
- GLP compliance:
- yes
Test material
- Reference substance name:
- (±)-13-ethyl-3-methoxygona-2,5(10)-dien-17β-ol
- EC Number:
- 213-860-9
- EC Name:
- (±)-13-ethyl-3-methoxygona-2,5(10)-dien-17β-ol
- Cas Number:
- 1038-28-4
- Molecular formula:
- C20H30O2
- IUPAC Name:
- 13-ethyl-3-methoxy-4,6,7,8,9,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol (non-preferred name)
- Details on test material:
- - Name of test material (as cited in study report): Ethyldienol
- Analytical purity: 93.5%
- Lot/batch No.: 15005201
Constituent 1
Sampling and analysis
- Analytical monitoring:
- no
Test solutions
- Vehicle:
- yes
Test organisms
- Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
Study design
- Test type:
- flow-through
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 24 h
- Dose descriptor:
- EC100
- Effect conc.:
- > 1 - ca. 2 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- behaviour
- Duration:
- 24 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 1 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
Any other information on results incl. tables
- Sublethal observations / clinical signs:
Table 1: Effects on behaviour of Zebra fish (n=1 0), exposed to ZK 47.569
Test concentration of ZK 47,569 (mg/L) nominal Fish showing total apathy (% of surviving animals) 3 hours 6 hours 24 hours 0 0 0 0 1 0 0 0 2 10 10 100 3,6 90 100 100 8,1 90 100 100
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- An LC50 for ZK 47.569 could not be calculated, since no concentration-dependent mortality
was observed in this study but lies between 1 and 2 mg/L. However, clear effects (total apathy
in all fish) were observed after a 24-hour exposure at concentrations of 2.0, 3.6, and 8.1 mg/I
(nominal). The NOEC/24 hours is therefore 1 mg/L.
It is anticipated that the degree of effects and the clear concentration relationship gives
sufficient information on the acute toxicity of ZK 47.569 to fish. A further test over the full test
period of 96 hours is not considered to add relevant information. - Executive summary:
The purpose of this study was to determine the acute toxicity/96 hours of the test compound
Ethyldienol to the Zebra fish (Brachydanio rerio). The study was conducted in agreement with
the test guideline of the OECD, no. 203 "Fish, Acute Toxicity Test".
Ten Zebra fish each were exposed to four concentrations of the test substance and the dilution water for aperiod of 48 hours under flow-through conditions. The test solutions were prepared using 0.2 g Tween 80/L as a vehicle. The same vehicle
concentration was used for the control.
The following nominal test concentrations were selected: 1.0, 2.0, 3.6 and 8.1 mg/L. No chemical analysis was performed. However, it is assumed that under the given flow-through conditions > 80% of the nominal concentration of test compound was maintained taking in account the flow-rate and the hydrolytical stability.
Mortalities and visual abnormalities were recorded at 3, 6, 24, and 48 hours.
The results of the test after 48 hours could not be evaluated due to a technical defect of the
test system. Therefore, only the data related to the 24-hour exposure time are reported.
Mortality (one fish) was observed in the test concentration of 3.6 mg/L within 24 hours.
A concentration- and time-dependent occurrence of total apathy was noted at concentrations
of 2.0 to 8.1 mg/L. Additionafly, two fish were found to have lost equilibrium in the concentration
of 3.6 mg/L. The fish in the control group were free from abnormal effects.
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