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EC number: 263-193-2 | CAS number: 61791-59-1
- 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
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: A defined amount of the test substance (stock solution concentration = 500 mg/L) was weighed into a measuring flask and the total volume was filled up with dilution water. The test bottles were conditioned about 15 min before the test was started.
- Differential loading: yes
- Controls: yes, dilution water served as negative control - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: water flea
- Source: Umwelt-Bundesamt, Berlin, Germany
- Age of Daphnia at test initiation: 6 - 24 h
- Feeding during test: no
BREEDING
- Breeding conditions: diffuse, continuous illumination, 20 °C
- Food type: freshwater alga suspension (Scenedesmus subspicatus)
- Frequency: daily - Test type:
- not specified
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Test temperature:
- 20.5 °C
- pH:
- 0 h: 7.2 (control), 7.4 - 7.5 (test solutions)
48 h: 7.4 (control), 7.3 - 7.4 (test solutions) - Dissolved oxygen:
- 0 h: 6.2 mg/L (control), 5.7 - 6.0 mg/L (test solutions)
48 h: 5.6 mg/L (control), 5.1 - 5.6 mg/L (test solutions), corresponding to 63% of the air saturation - Nominal and measured concentrations:
- nominal: control, 1.0, 2.5, 5.0, 10, 25, 50 and 100 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel: beakers
- Test solution volume: 10 mL
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: distilled water; Ca/mg ratio: 4:1, sum = 2.5 mmol/L
- Culture medium different from test medium: no
- Intervals of water quality measurement: 24 h. The pH-values and O2 concentration were measured before and after the test
OTHER TEST CONDITIONS
- Adjustment of pH: no
- Photoperiod: the test was performed in the dark
EFFECT PARAMETERS MEASURED:
- Immobilization: at 24 h and 48 h - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Key result
- 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:
- - Other biological observations: no
- Mortality of control: 0%
- Any observations that might cause a difference between measured and nominal values: no - Results with reference substance (positive control):
- - Results with reference substance valid? yes
- Relevant effect levels: EC50 (24 h) = 1.2 mg/L - Reported statistics and error estimates:
- The statistical evaluation was based on a Probit analysis. The calculation of the Probit values was performed with the computer program "Dosis 50". In this program the experimentally determined percentages in the range from 1 - 99% can be used for the calculation of the Probit values and so for the evaluation of the effective concentrations. For the experimentally determined percentages of 0% and 100% there are no Probit values defined. For the calculation of the Probit values of these percentages the percentages 1% and 99% were used.
Reference
The highest tested concentration of test substance producing no immobile daphnia under test conditions after 48 h was 1.0 mg/L.
The lowest tested concentration of test substance producing 100 % immobile daphnia under test conditions after 48 h was 25 mg/L.
Table 1. Study results.
Concentration of the test substance [mg/L] |
Immobilization [%] |
pH-value |
O2 [mg/L] |
|||
24 h |
48 h |
Before test |
After test |
Before test |
After test |
|
100 |
100 |
100 |
7.5 |
7.3 |
5.9 |
5.1 |
50 |
75 |
100 |
7.5 |
7.3 |
5.9 |
5.1 |
25 |
65 |
100 |
7.5 |
7.4 |
6.0 |
5.1 |
10 |
25 |
45 |
7.5 |
7.4 |
6.0 |
5.1 |
5.0 |
10 |
15 |
7.5 |
7.4 |
5.7 |
5.6 |
2.5 |
0 |
5 |
7.4 |
7.4 |
6.0 |
5.5 |
1.0 |
0 |
0 |
7.4 |
7.4 |
5.8 |
5.6 |
control |
0 |
0 |
7.2 |
7.4 |
6.2 |
5.6 |
Description of key information
EC50 (48 h) = 10.0 mg/L (nominal, Daphnia magna, OECD 202)
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 10 mg/L
Additional information
One GLP-study according to OECD 202 investigating the short-term toxicity of Glycine, N-methyl-, N-coco acyl derivatives, sodium salts (CAS 61791-59-1) to aquatic invertebrates is available. The test organism Daphnia magna was exposed to seven nominal test concentrations ranging from 1.0 - 100 mg/L (1.0, 2.5, 5.0, 10, 25, 50 and 100 mg/L) under controlled conditions for 48 h. No analytical measurement was conducted. Immobilisation was recorded every 24 h and compared to the negative control. After 48 h immobilisation was observed at concentrations ≥ 2.5 mg/L. The derived nominal EC50 value after 48 h was 10.0 mg/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.
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