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EC number: 264-129-6 | CAS number: 63405-85-6
- 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
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Study initiation date - 16 August 1990; Experiment start date - 12 September 1990; Experiment end date - 14 September 1990; Study completion date - 25 February 1991
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: EEC Directive 84/449, L 251, Part C 2., pp. 155 - 159: "Acute Toxicity for Daphnia".
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: U.S. Environmental Protection Agency, Pesticide Assessment Guidelines, Subdivision E. Hazard Evaluation: Wildlife and Aquatic Organisms : Acute Toxicity Test for Freshwater Invertebrates, EPA- 540/9-85-005, June, 1985
- Deviations:
- no
- GLP compliance:
- yes
- Specific details on test material used for the study:
- Name: FAT 20004/H
Batch no: EN 317
Expiration: June 1995. - Analytical monitoring:
- yes
- Details on sampling:
- Analytical measurements of the test article were performed in the stock solution and in test media of the nominal concentrations 0.65, 2.5 and 10.0 mg/l at the start and the end of the test by sampling a part of the stock solution and freshly prepared test media and media, which were incubated during test duration under the same conditions as in the test itself.
- Vehicle:
- no
- Details on test solutions:
- A stock solution was prepared by dissolving the test article in Dimethylformamide p.A. (100 g/l). The stock solution was diluted in a series of sequential dilutions with the solvent to add the same volumes of solvent (0.1 ml/l) to each test solution.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- The study was performed with young Daphnia magna Straus (6-24 hours old), bred in the laboratories of RCC under standardized conditions. The parental Daphnia were maintained in the same reconstituted water as in the test for at least 24 hours prior to the start of the test.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Hardness:
- 2.5 mmol/l as CaC03
- Test temperature:
- 19.5 - 19.8 °C (measured at the start and the end of the test)
- pH:
- 8.0 - 8.3
- Dissolved oxygen:
- >9.8 mg/L
- Nominal and measured concentrations:
- The nominal concentrations tested were 0.65, 1.25, 2.5, 5.0 and 10.0 mg test article/l, a solvent control group and a control without any additions.
- Details on test conditions:
- Test procedure: static
Duration: 48 hours
Temperature: 19.5-19.8 °C
Oxygen concentration: >9.8 mg/L
pH-value: 8.0 - 8.3
Exposure to light: 16 hours/day, about 200 - 600 Lux - Reference substance (positive control):
- not specified
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 10 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 10 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- After 24 and 48 hours of exposure no immobilisation was observed in the control and at 100 mg/L.
- Results with reference substance (positive control):
- EC50(24 h) between 1.0 and 2.0 mg/L
Reference substance: potassium dichromate - Reported statistics and error estimates:
- The 24 h and 48 h EC50 are the estimated concentrations where 50 % of the daphnids were immobilised after 24 and 48 hours, respectively.
No statistical evaluation was indicated since no immobilisation occurred at the limit test concentration of 100 mg/L.
The NOEC was established based on the highest concentration at which the immobilisation is not higher than the allowed control immobilisation (≥10 % immobilisation). - Validity criteria fulfilled:
- not specified
- Conclusions:
- The NOEC (highest concentration tested without toxic effect) of FAT20004/H was determined to be 10.0 mg test article/L. The 48 hour EC 50 could not be specified.
- Executive summary:
The acute toxicity of FAT 20004/H to Daphnia magna was determined in a 48-hour static test according to the OECD Guideline for Testing of Chemicals, Section 2, No. 202, adopted 4 April 84, the EEC Directive 84/449, L 251, Part C 2, and to the Guideline of the U.S. Environmental Protection Agency, Pesticide. Assessment Guidelines, Subdivision E, EPA-540/9-85-005, June, 1985. The test was performed in compliance with the Good Laboratory Practice Regulations. The nominal concentrations tested were 0.65, 1.25, 2.5, 5.0 and 10.0 mg test article, a solvent control group and a control without any additions. In the control, the solvent control group and in the test concentrations of nominal 0.65 to 5.0 mg test article, no immobility or mortality was observed during test duration. In the highest concentration tested of 10.0 mg test article (as the highest concentration as possible to dissolve in dimethylformamid at room temperature and an addition of 100 ul solvent stock solution to 1 litre test medium) the immobility rate was 5 % after 24 and 48 hours test duration. Because of this low immobilization rate, the NOEC (highest concentration tested without toxic effect) of FAT 20004/H was determined to be 10.0 mg test article. The 48 hour EC 50 could not be specified.
Reference
Influence of FAT 20004/H on immobilization of Daphnia magna:
Nominal Conc. Of test material (mg/l) | No. of Daphnia tested | No. of immobilixzed Daphnia after: | % of immobilized Daphnia after: | ||
24 h | 48 h | 24 h | 48 h | ||
Control | 20 | 0 | 0 | 0 | 0 |
Solvent control | 20 | 0 | 0 | 0 | 0 |
0.65 | 20 | 0 | 0 | 0 | 0 |
1.25 | 20 | 0 | 0 | 0 | 0 |
2.5 | 20 | 0 | 0 | 0 | 0 |
5 | 20 | 0 | 0 | 0 | 0 |
10 | 20 | 1 | 1 | 5 | 5 |
Description of key information
The NOEC (highest concentration tested without toxic effect) of FAT20004/H was determined to be 10.0 mg test article/l. The 48 hour EC50 could not be specified. Hence LC50 is concluded to be greater than 100 mg/L.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 100 mg/L
Additional information
The acute toxicity of FAT 20004/H to Daphnia magna was determined in a 48-hour static test according to the OECD Guideline for Testing of Chemicals, Section 2, No. 202, adopted 4 April 84, the EEC Directive 84/449, L 251, Part C 2, and to the Guideline of the U.S. Environmental Protection Agency, Pesticide. Assessment Guidelines, Subdivision E, EPA-540/9-85-005, June, 1985. The test was performed in compliance with the Good Laboratory Practice Regulations. The nominal concentrations tested were 0.65, 1.25, 2.5, 5.0 and 10.0 mg test article/l, a solvent control group and a control without any additions. In the control, the solvent control group and in the test concentrations of nominal 0.65 to 5.0 mg test article, no immobility or mortality was observed during test duration. In the highest concentration tested of 10.0 mg test article (as the highest concentration as possible to dissolve in dimethylformamide at room temperature and an addition of 100 µl solvent stock solution to 1 litre test medium) the immobility rate was 5 % after 24 and 48 hours test duration. Because of this low immobilization rate, the NOEC (highest concentration tested without toxic effect) of FAT 20004/H was determined to be 10.0 mg test article. The 48-hour EC 50 could not be specified.
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