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EC number: 415-450-7 | CAS number: 126213-50-1
- 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

Short-term toxicity to aquatic invertebrates
Administrative data
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 22.2.-11.3.2010
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This study was carried out in accordance with internationally valid GLP principles.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 010
- Report date:
- 2010
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Deviations:
- yes
- Remarks:
- See overall remarks.
- GLP compliance:
- yes
Test material
Reference
- Name:
- Unnamed
- Type:
- Constituent
- Details on test material:
- - Name of test material (as cited in study report): 3,4-Ethylenedioxythiophene
- Comercial name. EDOT
- Substance type: pure organic substance
- Physical state: liquid near colourless to pale yellow
- Analytical purity: > 99%
- Lot/batch No.: 091201
- Expiration date of the lot/batch: 21.1.2011
- Storage condition of test material: Keep in dark at room temperature. Stored in amber glass bottles under the argon atmosphere. Minimalize time for handling with substance without protective argon atmosphere as possible. Maximal time without protective atmosphere is 30 min.
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- - Test solution nominal concentration: 0.5, 1, 2, 5, 10, 23, 50 mg/L
- Sample storage conditions before analysis: All samples for analysis were delivered in transport box to analytical laboratory immediately after preparation and after each test period (0-24 hours and 24-48 hours). An analysis of samples was started immediately after delivery. All samples were stored at laboratory temperature.
Test solutions
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: The stock solution of the test substance was prepared in the dilution water. 100 mg of the test substance was weighed into 1000 mL of the dilution water for the preliminary test and the full semi-static test. The stock solutions were stirred for period 30 min. on a magnetic stirrer.
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Daphnia magna
- Strain: Straus
- Source: own laboratory breeding
- Age at study initiation (mean and range, SD): young daphnia born in 24 hr
- Method of breeding: aperiodic parthenogenesis
- Feeding during test: no
ACCLIMATION
- Acclimation period: The grow-up gravid females are separated into dilution water. Young daphnia born in 24 hours are segregated to the handling container from which they entered the experiment.
- Acclimation conditions: same as test
- Type and amount of food: a mixture of algae
- Feeding frequency:
- Health during acclimation (any mortality observed): At handling a care should be taken of not to penetrate the air under animal’s shell.
Study design
- Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
Test conditions
- Hardness:
- Test solution 1:
Content of (Ca+Mg) in dilution water 2.47 mmol/L
Test solution 2 (renewal the test solutions after 24 hrs):
Content of (Ca+Mg) in dilution water 2.48 mmol/L - Test temperature:
- 20+/-2 °C
- pH:
- 7.8
- Dissolved oxygen:
- Test solution 1: 8.5 mg.L-1 at temperature of 20.3 °C
Test solution 2 (renewal the test solutions after 24 hrs): 9.1 mg.L-1 at temperature of 20.5 °C - Nominal and measured concentrations:
- See table 2
- Details on test conditions:
- TEST SYSTEM
- Test vessel: open beakers (50 mL)
- Aeration: no
- Renewal rate of test solution: The test solutions were renewed after 24 hrs.
- No. of organisms per vessel: 10
- No. of vessels per concentration (replicates): 2
- No. of vessels per control (replicates): 2
- Biomass loading rate: one daphnia per 5 mL of test solution (least 2 ml per individual)
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Standard dilution water was prepared just before the test.
- The dilution water should be of pH 7.8 +/- 0.2. The sum of Ca + Mg ions should be approx. 2.5 mmol.L-1.
- Total organic carbon:
- Ca/mg ratio: 2.48 mmol.L-1
- Conductivity: 0.171 mS.m-1
OTHER TEST CONDITIONS
- Lighting: natural variation of daily light and dark
EFFECT PARAMETERS MEASURED: immobilisation of daphnia after 24 and 48 hours
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2.2
- Range finding study:
The preliminary test was performed in range of test substance nominal concentrations 1 – 100 mg•L-1. The analytical results from the preliminary test showed, that the test substance 3,4-Ethylenedioxythiophene was not stable in dilution water in conditions of the test. Based on the instability and toxicity of the test substance found in preliminary test, the full semi-static test was performed in appropriate concentration range. - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 19.4 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 13.5-25.3 mg/L
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 13 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 11.7-14.4 mg/L
- Duration:
- 24 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.95 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.95 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 24 h
- Dose descriptor:
- EC100
- Effect conc.:
- > 41.7 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC100
- Effect conc.:
- > 41.7 mg/L
- Nominal / measured:
- meas. (TWA)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Results with reference substance (positive control):
- - Results with reference substance valid: yes. The immobilisation of test species in reference substance solution expressed as EC50 fits into the accepted range in the interlaboratory tests.
- EC50: 48 hour – EC50 = 0.98 mg.L-1 (95 % confidence limit: 0.74 – 1.23 mg.L-1).
Any other information on results incl. tables
EVALUATION OF RESULTS
The value of EC50 was calculated by means of software “Toxicita”(product of Water Research Institute, Ostrava, Czech Republic). The NOEC and EC100 values are identified by direct observation.
Time weighted mean concentrations were used for all evaluations and results.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- no
- Remarks:
- See Overall remarks.
- Executive summary:
The test substance, 3,4-Ethylenedioxythiophene, was tested in acute immobilisation test on Daphnia magna.
The test was performed according to method C.2 – Daphnia sp. Acute Immobilisation Test, Council Regulation (EC) No. 440/2008, published in O.J.L 142, 2008.
The preliminary test was performed in range of test substance nominal concentrations 1 – 100 mg.L-1. The analytical results from the preliminary test showed, that the test substance 3,4-Ethylenedioxythiophene was not stable in dilution water in conditions of the test. Based on the instability and toxicity of the test substance found in preliminary test, the full semi-static test was performed in appropriate concentration range.
The full semi-static test was performed in range of test substance nominal concentrations 0,5 - 50 mg.L-1. The test solutions were renewed after 24 hours. The test substance content was measured at each test concentration at the start of the test, after 24 hours (before and after renewal), and at the end of the test.
For all evaluations and results time weighted mean concentrations were used.
Test results:
24 hour - EC50 = 19.4 mg.L-1 (95% confidence limit: 13.5 – 25.3 mg.L-1) (time-weighted mean concentration)
48 hour - EC50 = 13.0 mg.L-1 (95% confidence limit: 11.7 – 14.4 mg.L-1) (time-weighted mean concentration)
24 hour - NOEC = 0.95 mg.L-1 (time-weighted mean concentration)
48 hour - NOEC = 0.95 mg.L-1 (time-weighted mean concentration)
24 hour - EC100 > 41.7 mg.L-1 (time-weighted mean concentration)
48 hour - EC100 = 41.7 mg.L-1 (time-weighted mean concentration)
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