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EC number: 215-958-7 | CAS number: 1461-22-9
- 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
Link to relevant study record(s)
- Endpoint:
- toxicity to microorganisms
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- Not specified
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Method given but not done to a recognised guideline. Limited information on test material. No information on GLP.
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The activated sludge used for all tests was obtained from a sequential batch reactor that was operated at sludge ages (θc) of 10 and 20 days. The batch reactor was operated in a 24 h fill-and-draw cycle and was fed on synthetic sewage of fixed COD, 840 mg/L (Table 1).
Once steady state had been attained at each sludge age, activated sludge containing known concentrations of suspended solids was mixed in a 300 mL BOD bottle with the appropriate amount of feed to yield a food-to-microorganism (F/M) ratio of 0.1 mg COD mg^-1 MLVSS and the test material at various concentrations. Moreover, to inhibit autotrophic nitrifying bacterial respiration, thiourea was added to a final concentration of 10 mg/L. The control sample was prepared in the same manner but contained no organotin compounds. The flask was hermetically sealed by the probe of a membrane oxygen meter. The O2 concentration was recorded as a function of time up to concentrations of about 2 ppm, while the activated sludge was continuously mixed by means of a magnetic stirrer.
To estimate the effect of exposure time on inhibition of respiration rate, the above procedure was repeated but the addition of feed and the determination of respiration rate were done after the chosen exposure time had passed. In all tests pH was adjusted to 7.2 ± 0.2 and the temperature was 18 ± 0.5 °C. - GLP compliance:
- not specified
- Analytical monitoring:
- not specified
- Vehicle:
- not specified
- Test organisms (species):
- activated sludge
- Test type:
- not specified
- Water media type:
- not specified
- Limit test:
- no
- Total exposure duration:
- 20 d
- Duration:
- 10 d
- Dose descriptor:
- other: Ki
- Effect conc.:
- 4.1 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- other: Inhibition of respiration rate
- Duration:
- 20 d
- Dose descriptor:
- other: Ki
- Effect conc.:
- 42.5 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- other: Inhibition of respiration rate
- Validity criteria fulfilled:
- not specified
- Conclusions:
- The Ki values of activated sludge after 10 and 20 days are 4.1 and 42.5 mg/L respectively.
- Executive summary:
Inhibition of respiration rate of activated sludge heterotrophic microorganisms was determined for the test material.
An increase in sludge age or in the concentration of suspended solids reduces the observed inibition. Longer exposure seems to increase the inhibition of the test material during the first hours of exposure, while later the inhibition remains constant.
The Ki values of activated sludge after 10 and 20 days are 4.1 and 42.5 mg/L respectively.
Reference
The inhibition coefficient, Ki was determined for the test material according to Eq. (3) using a concentration of suspended solids equal to 1000 mg/L MLVSS and sludge age (θc) of 10 and 20 days. In all tests, the respiration rate was calculated for direct contact (t = 0) of inhibitor with biomass. The measured Ki values are shown in Table 2.
The values of Ki for the test material were higher in tests with a sludge age of 20 days than in those with a sludge age of 10 days, indicating a decrease in toxicity with increase in sludge age.
Description of key information
Key value for chemical safety assessment
Additional information
In a supporting study for this endpoint (Stasinakis et al, 2001), inhibition of respiration rate of activated sludge heterotrophic microorganisms was determined for the test material.
Inhibition of respiration rate of activated sludge heterotrophic microorganisms was determined for the test material.
An increase in sludge age or in the concentration of suspended solids reduces the observed inibition. Longer exposure was found to increase the inhibition of the test material during the first hours of exposure, while later the inhibition remains constant. The Ki (inhibition of respiration rate) values of activated sludge after 10 and 20 days are 4.1 and 42.5 mg/L respectively.
A reliability rating of 2 was assigned to this study, according to the criteria of Klimisch, 1997 as although there was limited information on test material and no information on GLP, the methodolgy is well documented.
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