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EC number: 206-616-8 | CAS number: 358-23-6
- 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:
- activated sludge respiration inhibition testing
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- From 30 March 2004 to 26 July 2004
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- Screening study according to the OECD TG209
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
- Deviations:
- no
- GLP compliance:
- no
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- Two stock solutions at 2 g/L (expressed as triflic acid) were prepared by dissolving the test item in dechlorinated water (pH: 7.62). The pH of both stock solutions was 2.38.
One of these stock solutions was neutralized by addition of 267 mg of pure (100%) NaOH per g of triflic acid. The pH of this stock solution was 7.22 after neutralization.
Test solutions were prepared by further dilution of the appropriate stock solution with dechlorinated water.
The pH of the test solutions at 1000 mg/L were 6.17 when prepared from test item as is (without neutralization) and 7.65 when prepared from neutralized test item. - Test organisms (species):
- activated sludge of a predominantly domestic sewage
- Details on inoculum:
- Type: inoculum was collected from a water treatment works containing effluent from a predominantly domestic origin.
Reason for this choice: this inoculum is recommended in the OECD guideline.
Origin: the water treatment plant of Evreux (27000 Evreux, France) or (at additional cost) the water treatment plant Emeraude (SIARR) (76141 Petit-Quevilly, France).
Preparation: the inoculum will be left to settle and the supematant rejected. It will be filtered and washed with dechlorinated water if necessary. The dry matter weight was adjusted to 4 g/L ± 10% with dechlorinated water, when required.
Conditions of culture:
The inoculum may be retained for up to 4 days in the laboratory before use in the test provided that it is topped up with 50 mL/L of synthetic sewage feed, daily. The culture room conditions were as follows:
Temperature: 20°C ± 2°C; the temperature in the culture room were recorded continuously and records retained.
Synthetic sewage feed: is prepared using dechlorinated water and analytical grade reagents following OECD recommendations.
Aeration: clean air were bubbled through the inoculum at the rate of 0.5 to 1 L/min until the start of the test.
pH: is checked before use and buffered, if necessary, to pH 6.0 to 8.0 using NaHCO3 or HCL - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Hardness:
- 280 ± 20 mg/L as CaCO3.
- Test temperature:
- 20°C ± 2°C throughout the test.
- pH:
- 6.17 to 7.65
- Nominal and measured concentrations:
- Nominal: 0, 10, 100 and 1000 mg/L with and without pH adjustment.
- Details on test conditions:
- Conditions of test
Temperature: 20°C ± 2°C throughout the test; the temperature in the culture room was recorded continuously and records retained.
Illumination: no special precautions was taken during the test, although for inoculum stocked for up to four days, the stock vessel was kept away from light.
Dilution water: dechlorinated tap water was used, with a hardness of 280 ± 20 mg/L as CaC03.
Aeration: air was bubbled through each solution at the rate of 0.5 to 1 L/min until the start of the 02 concentration measurements.
Test system:
Groups of test and reference solutions and controls were up for the test:
- two control solutions containing inoculum at 1.6 g/L,
- three test concentrations containing the test item with pH adjustment (i.e. test item neutralization) at 10, 100 and 1000 mg/L and inoculum at 1.6 g/L,
- three test concentrations containing the test item without pH adjustment (i.e. test item as is) at 10, 100 and 1000 mg/L and inoculum at 1.6 g/L,
- three test concentrations containing the reference item (3,5-dichlorophenol) at 4, 12 and 36 mg/L and inoculum at 1.6 g/L.
Initially these solutions were prepared in test flasks and then immediately afterwards aerated for 3 hours before being transferred to an oxygen measuring apparatus.
Test method:
Bach concentration was prepared separately by adding 16 mL of sewage feed to each of the flasks which were made up to 300 mL with water only in the case of the control or a nominal mixture of water and test item (added by means of a stock solution) in the case of the test solutions. Each mixture was then made up to 500 mL by adding 200 mL of inoculum. As 200 mL of inoculum was added in a final volume of 500 mL, the organic material concentration from inoculum was 1.6 g/L (± 10%).
The same procedure was used to prepare the three solutions containing the reference item. The solutions are aerated at between 0.5 to 1 liter of air per minute using a Pasteur-pipette connected with a flexible tube to an air pump as an aeration device.
Solutions were prepared approximately every 15 minutes.
In order to verify the quality of the inoculum, the controls are prepared at the beginning (first control) and the end (second control) of the test.
After 3 hours of aeration/contact time, the contents of each test flask was poured into the measuring apparatus and the oxygen concentration determined for a period of approximately 10 minutes using a chart recorder.
If the respiration rates of the test solutions of highest concentration (1000 mg/L with and without pH adjustment) were equivalent to the respiration rate of the first control (i.e. these rates are within 15% of each other), the oxygen consumption rate of the four other test solutions (10 and 100 mg/L with and without pH adjustment) was not determined. - Reference substance (positive control):
- yes
- Remarks:
- 3,5-dichlorophenol
- Key result
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth inhibition
- Remarks on result:
- other: neutralised or not
- Key result
- Duration:
- 3 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Results with reference substance (positive control):
- The 3h EC50 of the reference item was 11.7 mg/L.
- Validity criteria fulfilled:
- yes
- Remarks:
- the two control respiration rates are within 15% of each other; the EC50 (3 hours) of 3,5-dichlorophenol is in the accepted range 5 to 30 mg/L.
- Conclusions:
- Trifluoromethanesulfonic acid is not harmful to microorganisms.
- Executive summary:
The objective of the study was to assess the effect of the test item trifluoromethanesulfonic acid on the respiration of activated sewage sludge, over a period of 3 hours.
The criterion measured was the inhibition of the respiration rate of the activated sludge, exposed to different concentrations of the test item, and expressed as a percentage of the control.
From these values, the EC50 (concentration at which respiration rate is 50% of that in the control) was calculated.
The 3h EC50 of the reference item was 11.7 mg/L in this study. Therefore, the criterion for validation of the inoculum is fulfilled.
The highest tested concentration of the test item, i.e. 1000 mg/L, did not inhibited the respiration rate of the inoculum. This concentration can therefore be considered as a NOEC.
The 3h EC50 of the test item, with test item as is or neutralized, was > 1000 mg/L.
In these conditions, trifluoromethanesulfonic acid is not harmful to microorganisms.
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Justification for type of information:
- The read-across justification is provided in the attached document.
- Reason / purpose for cross-reference:
- read-across source
- Key result
- Duration:
- 3 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 1 000 mg/L
- Conclusions:
- By analogy with its degradation product in water, the 3-hour NOEC value of trifluoromethanesulfonic anhydride for the inhibition of the respiration rate of activated sludge is considered to be >= 1000 mg/L.
Referenceopen allclose all
Respiration rate:
|
Concentration (mg/L) |
Respiratory rate (mg O2.L-1.h-1) |
Inhibition (%) |
Control 1 |
0 |
42 |
|
Control 2 |
0 |
42 |
|
Reference item |
4 |
38 |
10 |
|
12 |
18 |
57 |
|
36 |
6 |
86 |
Triflic acid With pH adjustment |
10 |
ND |
|
100 |
ND |
|
|
1000 |
42 |
0 |
|
Triflic acid without pH adjustment |
10 |
ND |
|
100 |
ND |
|
|
1000 |
42 |
0 |
ND: Not determined. The respiration rate of the test solution of highest concentration (1000 mg/L) was equivalent to the respiration rate of the first control (i.e. these rates were within 15% of each other). Therefore, the oxygen consumption rate of the test solutions of lowest concentrations (10 and 100 mg/L) was not determined.
Description of key information
Trifluoromethanesulfonic anhydride being rapidly and completely hydrolysed in water, the effect concentration obtained with its degradation product, i.e. trifluoromethanesulfonic acid, is considered as relevant for the assessment of its aquatic toxicity.
Key value for chemical safety assessment
- EC10 or NOEC for microorganisms:
- 1 000 mg/L
Additional information
The read-across justification with trifluoromethanesulfonic acid is provided in the attached document in the endpoint study record.
The assessment of the effect of the test item trifluoromethanesulfonic acid on the respiration of activated sewage sludge was performed over a period of 3 hours according to a method equivalent to the OECD TG 209.
The highest tested concentration of the test item, i.e. 1000 mg/L, did not inhibit the respiration rate of the inoculum. This concentration can therefore be considered as a NOEC.
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