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EC number: 820-064-0 | CAS number: 13095-67-5
- 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
Appearance / physical state / colour
Administrative data
- Endpoint:
- appearance / physical state / colour
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Informaiton taken from other test report in which the test item appearance is reported.
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Reference
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 13.02-09.03.2018
- 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)
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- The analytical verification of test item concentrations in daphnid test medium was done by analysing the content of Dipotassium malonate in the samples during the test. Analytical samples were analysed from the test item concentration and control at test start and 48 hours from aged solutions.
- Vehicle:
- no
- Details on test solutions:
- - Test medium: reconstituted test water consisting of analytical grade salts dissolved in purified water (ISO test water)
- pH-value of the control (untreated test medium): 7.42
- dissolved oxygen concentration: 9.4 mg/L
- total hardness: 13°dH (232 mg/L as CaCO3) - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- - Daphnia magna Straus, Clone V, max. 24 hours old
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Post exposure observation period:
- none
- Hardness:
- total hardness 140 - 250 mg/L (as CaCO3), corresponding to 7.8 - 14°dH
- Test temperature:
- 18.9 – 19.5 °C
- pH:
- 7.42 – 7.77
- Dissolved oxygen:
- ≥ 9.0 mg/L
- Salinity:
- /
- Conductivity:
- not specified
- Nominal and measured concentrations:
- Nominal Concentration of the test item (100 mg/L, 0h fresh and 48h aged): 100 mg/L
Final Concentration µg/mL: 98.9 (0h fresh) and 96.2 (48h aged) - Details on test conditions:
- TEST SYSTEM
- Test vessel: 100 mL glass vessels
- Type: covered with a glass plate
- Fill volume: ca. 50 mL
- Aeration: none
- No. of organisms per vessel: 20
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: reconstituted test water consisting of analytical grade salts dissolved in purified water (ISO test water)
OTHER TEST CONDITIONS
- Photoperiod: 16 hours light / 8 hours darkness daily
- Light intensity: not specified
EFFECT PARAMETERS MEASURED (with observation intervals if applicable): immobilisation.
- Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate (1.00 mg/L, 2.00 mg/L)
- Key result
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: immobilisation
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: immobilisation
- Details on results:
- - Validity Criteria of the Study:
-- Control immobilisation: The percentage of immobilisation should be ≤ 10 %. In this study the control immobilisation was 0 %
-- Oxygen concentration: The dissolved oxygen concentration at the end of the test should be ≥ 3 mg/L in all test units. In this test, the dissolved oxygen concentration at the end of the test was ≥ 9.0 mg/L
- Biological Results:
-- After 24 hours of exposure no immobilisation was observed in the control and at 100 mg/L
-- After 48 hours of exposure no immobilisation was observed in the control and at 100 mg/L
-- No behavioural changes could be observed
- Analytical Results:
The measured content of dipotassium malonate was 99% of nominal and the aged measured content was 96% of nominal. Since the content of dipotassium malonate in the samples was between 80 and 120% of nominal the toxicological endpoints were evaluated using nominal concentrations. - Results with reference substance (positive control):
- The results indicate an EC50 (24 h) of the reference item potassium dichromate between 1.00 and 2.00 mg/L.
Since the results are in accordance with the requirements of the OECD guideline 202 and fall within the historical data generated with the reference item at the testing facility, the daphnids were suitable for the determination of the toxicological effects of the test item. - Reported statistics and error estimates:
- All toxicological endpoints were evaluated using nominal concentrations.
- Validity criteria fulfilled:
- yes
- Conclusions:
- According to the results of the test, the EC50 (48 h) for immobilisation was assumed to be > 100 mg/L (nominal). The corresponding NOEC (48 h) was 100 mg/L (nominal).
- Executive summary:
The objectives of this study were to determine the immobilisation effect of the test item Dipotassium malonate on the water flea Daphnia magna under worst-case exposure conditions after the exposure to test solutions and observation of immobilisation after 24 and 48 hours of exposure under static conditions. The study was performed according to OECD test guideline 202 (2004) and in compliance to GLP.
The test was performed as a static limit test with twenty test organisms per treatment (4 replicates of 5 test organisms each). The duration of the test was 48 hours. Endpoints reported are the EC50and the NOEC after 24 and 48 hours.
Following a static non-GLP range-finding test a static limit test with the nominal concentration 100 mg/L and control was performed. Temperature, pH-value and oxygen concentration of the test solutions measured after 0, 24 hours aged and 48 hours are reported. Hardness of the test medium (untreated control) was measured on the day of application.
Analytical samples taken at 0 hours (initial value) and 48 hours from aged test solutions were analysed from control and the test item concentration.
Due to a lack of immobilisation, the values for EC50were not determined statistically. The NOEC was established based on the highest concentration at which the immobilisation is not higher than the allowed control immobilisation (≤ 10 % immobilisation).
All validity criteria were fulfilled.
According to the results of the test, the EC50 (48 h) for immobilisation was assumed to be > 100 mg/L (nominal). The corresponding NOEC (48 h) was 100 mg/L (nominal).
EC50and NOEC-values of daphnids exposed to the test item evaluated using nominal concentrations
Endpoint |
Dipotassium malonate [mg/L] |
|
|
24 h |
48 h |
NOEC |
100 |
100 |
EC50 |
> 100 |
> 100 |
95 % confidence limit of EC50 |
- |
- |
- not applicable
Analytical Results: Determined concentration of Dipotassium malonate
Dipotassium malonate nominal [mg/L] | Sampling [h] | analyte | ||||
[mg/L] | % of nominal | |||||
Control | 0 fresh | n.d. | - | |||
48 aged | n.d. | - | ||||
100 | 0 fresh | 98.8 | 99 | |||
48 aged | 96.4 | 96 |
- = not calculated; n.d. = not detectable; LOQ = 0.400 mg/L Dipotassium malonate
Results of the test, 24 h values
|
Nominal test item concentration [mg/L] |
|
|
Control |
100 |
|
Immobilised daphnids after 24 h |
|
Replicate 1 |
0 |
0 |
Replicate 2 |
0 |
0 |
Replicate 3 |
0 |
0 |
Replicate 4 |
0 |
0 |
Σ |
0 |
0 |
% |
0 |
0 |
Results of the test, 48 h values
|
Nominal test item concentration [mg/L] |
|
|
Control |
100 |
|
Immobilised daphnids after 48 h |
|
Replicate 1 |
0 |
0 |
Replicate 2 |
0 |
0 |
Replicate 3 |
0 |
0 |
Replicate 4 |
0 |
0 |
Σ |
0 |
0 |
% |
0 |
0 |
Results of the toxic reference test
K2Cr2O7 |
24 h |
48 h |
||||
[mg/L] |
1.00 |
2.00 |
1.00 |
2.00 |
||
|
immobilised daphnids |
|||||
Replicate 1 |
2 |
5 |
5 |
5 |
||
Replicate 2 |
0 |
5 |
2 |
5 |
||
Replicate 3 |
1 |
5 |
5 |
5 |
||
Replicate 4 |
2 |
5 |
5 |
5 |
||
S |
5 |
20 |
17 |
20 |
||
% |
25 |
100 |
85 |
100 |
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 018
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Observation of test material made during daphnia test.
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Dipotassium propanedioate
- EC Number:
- 820-064-0
- Cas Number:
- 13095-67-5
- Molecular formula:
- C3H2K2O4
- IUPAC Name:
- Dipotassium propanedioate
Constituent 1
Results and discussion
- Physical state at 20°C and 1013 hPa:
- solid
Form / colour / odour
- Key result
- Form:
- solid
- Colour:
- white
- Substance type:
- organic
Applicant's summary and conclusion
- Conclusions:
- The test item is a white solid.
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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