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EC number: 619-816-9 | CAS number: 128446-33-3
- 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:
- 2002-05-15 until 2002-07-22
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: OECD study under GLP
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 002
- Report date:
- 2002
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- Cavasol W6 HP
- IUPAC Name:
- Cavasol W6 HP
- Details on test material:
- - Name of test material (as cited in study report): CAVASOL W6 HP
- Physical state: solid powder
- Impurities (identity and concentrations): as stated in substance data
- Composition of test material, percentage of components: as stated in substance data
- Lot/batch No.: 63B001
- Expiration date of the lot/batch: 2003-02-28
- Stability under test conditions: stable
- Storage condition of test material: in original container, at room temperature, in the dark
Constituent 1
Study design
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic (adaptation not specified)
- Details on inoculum:
- - Source: domestic waste water treatment plant (Waterschaap de Maaskant, 's Hertogenbosch, The Netherlands)
- Method of cultivation: sludge was washed, the supernatant liquid phase was decanted.
- Concentration of solids: 3.8 g/l in the concentrated sludge - Duration of test (contact time):
- 28 d
Initial test substance concentration
- Initial conc.:
- 12 mg/L
- Based on:
- ThOD/L
Parameter followed for biodegradation estimation
- Parameter followed for biodegradation estimation:
- CO2 evolution
- Details on study design:
- TEST CONDITIONS
- Composition of medium: in accordance with Guideline
- pH: 7.4 - 7.6
- pH adjusted: no
- Continuous darkness: yes
- Temperature: 22°C
TEST SYSTEM
- Culturing apparatus:2 litre all-glass brown coloured bottles
- Number of culture flasks/concentration: 2 bottles (test substance + inoculum), 2 bottles (inoculum), 1 bottle (reference compound sodium acetate + inoculum), 1 bottle (test substance + reference compound sodium acetate + inoculum)
- Test substance: test substance was directly mixed with test medium and allow to stir on a magnetic stirrer for about 6 hours in the dark; in this way the test substance reacted to the water-soluble hydrolysis product dicyclopentylsilanediol; concentration: 2.6 mg test substance/L + 0.5 ml inoculum/L test medium
- Method used to create aerobic conditions: aeration of test medium
SAMPLING
- Sampling frequency: measurement was performed on exposure days 0, 2, 5, 7, 9, 14, 19, 23, 27 and 29
CONTROL AND BLANK SYSTEM
- Inoculum blank: 0.5 ml filtered inoculum/L test medium
- Procedure control: 40 mg/l soium acetate + inoculum/ test medium
- Toxicity control: test substance + sodium acetate + inoculum
Reference substance
- Reference substance:
- acetic acid, sodium salt
Results and discussion
% Degradationopen allclose all
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 1
- Sampling time:
- 2 d
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 3
- Sampling time:
- 7 d
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 3
- Sampling time:
- 14 d
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 6
- Sampling time:
- 23 d
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 11
- Sampling time:
- 29 d
- Details on results:
- The reference compound sodium acetate was biodegraded by 60 % by exposure day 14 and reached an biodegradation rate of 70% by the end of the study, thus confirming suitability of the activated sludge. In the toxicity control, an average biodegradation of 35 % was noted within 14 days of exposure, thus not indicating a toxic effect of the test substance on the microorganisms.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- under test conditions no biodegradation observed
- Conclusions:
- Cavasol W6 HP is not readily biodegradable.
- Executive summary:
Cavasol W6 HP was investigated for its ready biodegradability in the "Modified Sturm Test" when exposed to aerobic activated sludge from a domestic waste water treatment plant over a period of 28 days. Under the test conditions Cavasol W6 HP was found to be not readily biodegradable over the 28 -day exposure period. The reference substance sodium acetate reached the level for ready biodegradability, thus confirming suitability of the activated sludge. In the toxicity control an biodegradation of only 35% was noted within 14 days of exposure, thus not indicating a toxic effect of the test substance on the microorganisms.
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