Registration Dossier
Registration Dossier
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: 228-351-7 | CAS number: 6236-40-4
- 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

Toxicity to microorganisms
Administrative data
- Endpoint:
- toxicity to microorganisms
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Aug - Nov 1994
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: According to DIN 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:
- DIN 38412-8 (Pseudomonas Zellvermehrungshemmtest)
- Deviations:
- no
- 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-17-one
- EC Number:
- 228-351-7
- EC Name:
- (±)-13-ethyl-3-methoxygona-2,5(10)-dien-17-one
- Cas Number:
- 6236-40-4
- Molecular formula:
- C20H28O2
- IUPAC Name:
- (3aS,3bR,9bS,11aS)-11a-ethyl-7-methoxy-1H,2H,3H,3aH,3bH,4H,5H,6H,9H,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-1-one
- Details on test material:
- - Name of test material (as cited in study report): Ethyldienon
- Analytical purity: 89.1%
- Lot/batch No.: 21400404
Constituent 1
Sampling and analysis
- Analytical monitoring:
- yes
Test solutions
- Vehicle:
- no
Test organisms
- Test organisms (species):
- Pseudomonas putida
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 16 h
Results and discussion
Effect concentrations
- Duration:
- 16 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 4 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- growth inhibition
Any other information on results incl. tables
The measurements showed that there is no growth inhibition of the bacterial population.
Table 1: Mean values of turbidity (expressed as TE/F) and growth inhibition as a function of the concentration
Concentration | TE/F ± standard deviation | Growth inhibition | ||
[mg/L] | [mean value (16 hours)] | -(%) | ||
Control | 359 | ± | 17,8 | 0 |
1 :1000 diluted | 355 | ± | 3,6 | 1,1 |
1 : 1 00 diluted | 352 | ± | 9 | 1,9 |
1 :10 diluted | 355 | ± | 27,5 | 1,1 |
Saturated, not diluted | 402 | ± | 0 | -12 |
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- Ethyldienon up to a saturated solution (approximately 4 mg/L) had no inhibitory effect on the growth of Pseudomonas putida. The slight increase of growth at the saturated concentration is not considered to be biologically relevant.
- Executive summary:
The purpose of this study was to determine the effects of the test compound Ethyldienon (ZK 28519) on the growth of the bacterium Pseudomonas putida. The study was conducted in agreement with the standard DIN 38412 L8, Mar. 91.
The test substance was incubated in an aqueous solution including nutrients with a bacterial population of Pseudomonas putida for a test duration of approximately 16 hours. The nutrient solution was made up of mainly nitrate, phosphates, carbohydrates, some trace elements and vitamins. A stock solution with a concentration of 1000 mg/L was prepared, stirred for 24 hours and filtered. This filtered stock solution was used for the highest test concentration. For further test concentrations the stock solution was diluted 1 :10, 1:100 and 1 :1000. Additionally, one control without the test substance was used. All test solutions including the control were incubated in triplicate. Furthermore, for each test concentration one test vessel was incubated without addition of the inoculum in order to analyse the inherent turbidity of the test compound. The concentration of the saturated, filtered solution was analysed with a TOC-analyser and subsequent calculation based on the structural formula.
As a parameter for the growth of the bacterial population, the turbidity of the test and control solutions was analysed photometrically at a wave-Iength of 436 nm.
The measurements showed that there is no growth inhibition of the bacterial population. On the contrary, there is a slight growth increase at the highest test concentration in comparison with the control group.
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.
