Registration Dossier
Registration Dossier
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 206-586-6 | CAS number: 355-43-1
- 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:
- 16.03.2007 to 19.06.2007
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 007
- Report date:
- 2007
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-6-iodohexane
- EC Number:
- 206-586-6
- EC Name:
- 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-6-iodohexane
- Cas Number:
- 355-43-1
- Molecular formula:
- C6F13I
- IUPAC Name:
- 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-6-iodohexane
- Test material form:
- liquid
Constituent 1
Sampling and analysis
- Analytical monitoring:
- yes
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- The study was performed with young daphnids of a clone of the species Daphnia magna Straus. A clone of this species (defined by the supplier as clone 5) was originally supplied by the University of Sheffield/UK in 1992. Since that time, the clone is bred in the laboratories of RCC in reconstituted water of the quality identical to the water quality used in the tests (in respect of pH, main ions, and total hardness) and under temperature and light conditions identical to those of the tests (see below).
At the start of the test, the daphnids used for the test were 6-24 hours old and were not first brood progeny.
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
Test conditions
- Hardness:
- Reconstituted test water: analytical grade salts were dissolved in purified
water to obtain the following nominal concentrations:
CaCb x 2H20
MgS04 x 7H20
NaHC03
KCI
Water Hardness
Alkalinity
2.0 mmol/L (= 294 mg/L)
0.5 mmol/L (= 123 mg/L)
0.75 mmol/L (= 65 mg/L)
0.075 mmol/L (= 5.8 mg/L)
2.5 mmol/L (= 250 mg/Las CaC03)
0.8 mmol/L
Ratio of Ca : Mg = 4 : 1 (based on molarity)
Na : K = 10 : 1 (based on molarity) - Test temperature:
- 20 °C during the test period (Table 3). The test was performed in a temperature-controlled room (room temperature continuously monitored).
- Dissolved oxygen:
- The test water was aerated prior to the start of the study until oxygen saturation was reached. During the test period the test water was not aerated.
- Reference substance (positive control):
- yes
- Remarks:
- For evaluation of the quality of the daphnia clone and the experimental conditions, potassium dichromate is tested as a positive control twice a year.
Results and discussion
Effect concentrations
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC0
- Effect conc.:
- >= 25 µg/L
- Conc. based on:
- act. ingr. (dissolved fraction)
- Basis for effect:
- other: lake of toxicity at water saturation
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- 48-hour ECO and 48-hour NOEC > loading rate: 100 mg/L (25 μg/L)
- Executive summary:
The acute toxicity of the test item Fluowet I 600 to Daphnia magna was determined in a 48-hour static test according to the EU Commission Directive 92/69/EEC, Part C.2 (1992) and the OECD Guideline for Testing of Chemicals, No. 202 (2004).
Due to the low water solubility of the test item, a supersaturated dispersion of the test item with the loading rate of 100 mg/L was continuously stirred at room temperature in the dark over one hour in a closed vessel. Then, the dispersion was filtered. The undiluted filtrate of the dispersion and dilutions 1: 16, 1 :8, 1 :4, and 1 :2 were used as test media. Additionally, a control was tested in parallel. All test vessels were completely filled and well closed to avoid losses of the test item caused by volatility.
The analytically measured test item concentrations in the analyzed test media samples (dilutions 1:16, 1:8, 1:4, 1:2 and the undiluted filtrate) amounted to 1.1, 3.2, 6.6, 14 and 35 μg/L at the start of the test. At the end of the test, only the concentration of the undiluted filtrate was analyzed due to the absence of a toxic effect. The measured concentration of Fluowet I 600 in the undiluted filtrate decreased to 18 μg/L after 48 hours. The biological results are related to the loading rate of 100 mg/L and the mean measured test item concentration of 25 μg/L, which was calculated as the geometric mean of the test item concentration in the undiluted filtrate measured at the start and the end of the test period.
The biological test results were as follows:
After 24 and 48 hours of exposure, no immobility of daphnids was observed in the control and at test item concentrations up to and including the loading rate of 100 mg/L (25 μg/L).
Consequently, neither the EC100 nor the EC50 could be determined due to the missing toxic effects of the test item up to the loading rate of 100 mg/L (25 μg/L). Thus, the toxicity was above the water solubility limit of the test item in the used test water.
48-hour ECO and 48-hour NOEC > loading rate: 100 mg/L (25 μg/L)
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
