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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
Biodegradation in water: screening tests
Administrative data
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Nov - Dec 1995
- 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:
- 1 996
- Report date:
- 1996
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
- 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-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:
- 11a-ethyl-7-methoxy-1H,2H,3H,3aH,3bH,4H,5H,6H,9H,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-1-ol
- Details on test material:
- - Name of test material (as cited in study report): Ethyldienol
- Analytical purity: 80.9 - 93.9%
- Lot/batch No.: mixed batches
Constituent 1
Study design
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic (adaptation not specified)
- Duration of test (contact time):
- 27 d
Initial test substance concentration
- Initial conc.:
- 10 mg/L
- Based on:
- DOC
Results and discussion
% Degradation
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 0
- Sampling time:
- 28 d
- Details on results:
- On the basis of the CO2 production in the toxicity control, the reference compound sodium
acetate was degraded to 72% on day 7 (~ 6 days of incubation) and was further degraded up
to 96% on day 29 (~ 27 days of incubation).
Any other information on results incl. tables
Table 1: Biological degradation (cumulative) in percent (corrected tor blank C02 production)
Test compound | Nominal concentration | Day of sampling | ||||||
of carbon | 4 | 7 | 10 | 14 | 18 | 23 | 28 | |
ZK 47569 | 10 mg/L | 0 | 0 | 1 | 0 | 0 | 0 | 0 |
Sodium acetate | 10 mg/L | -30 | -54 | -64 | -78 | -86 | -90 | -96 |
(reference) | ||||||||
ZK 47569 + sodium | 10 mg/L + | 15 | 27 | 33 | 38 | 43 | 45 | 48 |
acetate (toxicity control) | 10 mg/L |
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- under test conditions no biodegradation observed
- Conclusions:
- In accordance with the OECD guideline, the test compound ZK 47569 is not readily
biodegradable under the conditions of the test and it was not toxic to the microbes of activated
sludge. - Executive summary:
The purpose of this study was to determine the ready biodegradability of Ethyldienol (ZK 47569). The study
was conducted in agreement with the following test guideline: OECD guideline tor testing of chemicals, Ready biodegradability: C02-evolution test, no. 301B.
The test substance was incubated in an aqueous solution including nutrients with microorganisms trom a municipal sewage treatment plant for 27 days (start of treatment = day 1). The nutrient solutions were made up of phosphates, ammonium sulphate,
magnesium sulphate, iron chloride, ammonium chloride and calcium chloride, and added to the test solution.
The test substance was incubated in a concentration of 10 mg carbon/L in triplicate.
Additionally, a reference substance (sodium acetate) was tested according to the same
procedure, in order to verity the viability and activity of the degrading microorganisms.
Furthermore, a blank contral was tested in triplicate without any test or reference substance.
One further set was incubated with sodium acetate as 10 mg, carbon/L (reference substance)
plus test substance as 10 mg carbon/L representing toxicity control.
The biological degradation of the test and reference substances was evaluated by
measurement of the carbon dioxide (C02) produced during the test period. CO2 production
was determined on days 4, 7, 10, 14, 18, 23 and 29, and calculated as the percentage of total
CO2 that the test material could theoretically have produced, based on carbon content. The
blank CO2 production was subtracted for correction.
The test compound was practically not degraded.
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