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EC number: 701-043-4 | CAS number: -
- 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
Toxicity to aquatic algae and cyanobacteria
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: According to international guideline(s), GLP-compliant, performed in recognized contract research organization, no restrictions, fully adequate for assessment.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.3 (Algal Inhibition test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 850.5400 (Algal Toxicity, Tiers I and II) (January 2012)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: nominal 100 mg/L and control
- Sampling intervals: start and end of the test (0 and 72 h)
- Sampling method: samples were taken from flasks containing no algal cells
- Sample storage conditions before analysis: no storage prior to analysis - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: water accommodated fractions (WAFs)
A supersaturated solution was prepared by dispersing/dissolving the test item into the test medium (OECD Medium) at a nominal concentration of 100 mg/L. This dispersion was shaken for about 24 hours at approximately 30°C and then was equilibrated for about 24 hours at the test temperature. The non-dissolved test material was removed by filtration through a 0.22-µm filter to provide the WAF. - Test organisms (species):
- Raphidocelis subcapitata (previous names: Pseudokirchneriella subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- TEST ORGANISM
- Strain: 61.81 SAG (identical strains: CCAP 278/4; UTEX 1648; ATCC 22662)
- Source (laboratory, culture collection): SAG: Collection of Algal Cultures, Inst. Plant Physiology, University of Göttingen, GERMANY.
- Age of inoculum (at test initiation): Three days. Algal cells used for inoculation were in the exponential phase of growth.
- Method of cultivation: Algae are cultured under standardised conditions. The pre-culture was intended to give an amount of alga suspension suitable for the inoculation of test cultures. The pre-culture was incubated under the conditions of the study in an aerated Algal Growth Medium and used when still exponentially growing (after an incubation period of 3 days). The cell count of above culture was determined by microscopic method and this cell suspension was diluted with Algal Growth Medium to 10^7 cells/mL.
ACCLIMATION
- Acclimation period: 3 days (pre-culturing)
- Culturing media and conditions (same as test or not): same - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 72 h
- Hardness:
- 24 mg/L as CaCO3 (calulated)
- Test temperature:
- 22.9-23.2 °C (daily measurements in a flask filled with water and incubated under the test conditions)
22.6-23.4 °C (continuous measurements in the climatic chamber) - pH:
- test start (0 h): 7.8
test end (72 h): 8.7-9.0 - Nominal and measured concentrations:
- nominal loading rate: 100 mg test material/L as WAF
measured concentrations:
start: 2.8 ± 1.7 mg test material/L (n=3)
end: 9.5 ± 8.7 mg test material/L (n=3) - Details on test conditions:
- TEST SYSTEM
- Test vessel: 250 mL Erlenmeyer flasks containing 100 mL of inoculated test medium and covered with air-permeable stoppers
- Aeration/gaseous exchange: continuous shaking on an laboratory orbital shaker
- Initial cells density: 1x10⁴ cells/mL
- Control end cells density: 71 x10⁴ cells/mL
- No. of vessels per concentration (replicates): 6
- No. of vessels per control (replicates): 6
GROWTH MEDIUM
- Standard medium used: yes
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: deionised water
- Ca/Mg ratio: 1:1
- Culture medium different from test medium: no
OTHER TEST CONDITIONS
- Sterile test conditions: no
- Adjustment of pH: no
- Photoperiod: continuous illumination
- Light intensity and quality: about 8114 lux (equivalent to 110 µE/m2/s), provided by fluorescent lamps (spectral range 400-700 nm).
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : cell numbers counted at 24, 48 and 72 hours
- Determination of cell concentrations: counting chamber
- Algal cells were observed microscopically for abnormal appearance at 24, 48 and 72 hours.
TEST CONCENTRATIONS
- Range finding study
- Test concentrations: nominal loading rate of 100 mg/L (WAF) and dilutions 10, 1 and 0.1 mg/L
- Results used to determine the conditions for the definitive study: no inhibition of algal growth after 72 hours - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EL50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: growth rate, yield and biomass
- Remarks on result:
- other: results are expressed in terms of loading rates
- Key result
- Duration:
- 72 h
- Dose descriptor:
- NOELR
- Effect conc.:
- >= 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: growth rate, yield and biomass
- Remarks on result:
- other: results are expressed in terms of loading rates
- Details on results:
- - Exponential growth in the control (for algal test): yes
- Observation of abnormalities (for algal test): no microscopic abnormalities
- Any stimulation of growth found in any treatment: no
Control cultures:
- increase of biomass by a factor of: 71
- mean coefficient of variation for section-by-section specific growth rates (days 0-1; 1-2; 2-3): 11.9%
- coefficient of variation for the average specific growth rates during the test period (day 0-3): 0.77% - Results with reference substance (positive control):
- - Results with reference substance valid? yes
- 48-hour ErC50: 0.94 mg/L (95% confidence limits. 0.85-1.03 mg/L) - Reported statistics and error estimates:
- The section-by-section specific growth rates in the control cultures were assessed (calculated as the specific growth rates for each day during the course of the test (days 0-1, 1-2 and 2-3) and to demonstrate exponential growth for the entire study period.
The inhibition of alga growth was determined from the biomass (area under the growth curves, A), the average specific growth rate (r) and from the yield (y). Mean values and standard deviations were calculated for each concentration at the start, and at the end of the test using Excel for Windows software (Microsoft Co./One Microsoft Way/Redmond, WA 98052-6399).
The ErC50, EbC50 and EyC50 values of the test item were determined from the raw data.
Statistical comparisons of biomass, average specific growth rates and yield in control and in treated groups were carried out using 2 Sample t-Test (α = 0.05) by TOXSTAT software.
For the determination of the LOEC and NOEC, the calculated mean biomass, growth rates and yield at the test concentrations were tested on significant differences to the control values by 2 Sample t-Test (α = 0.05) by TOXSTAT software. - Validity criteria fulfilled:
- yes
- Remarks:
- Increase of biomass >16 after 72 hours; mean coefficient of variation for section-by-section specific growth rate <35%; coefficient of variation for average specific growth rate <7%.
- Conclusions:
- The results indicate that the test material is not toxic to algae up to the limits of its water solubility.
Reference
Table 1: Cell Number
Nominal loading rates (mg/L) |
Replicate number |
Cell number (x 104/mL) |
||
24 hours |
48 hours |
72 hours |
||
Control |
R1 |
3 |
16 |
68 |
R2 |
4 |
18 |
71 |
|
R3 |
5 |
21 |
69 |
|
R4 |
5 |
22 |
73 |
|
R5 |
4 |
18 |
70 |
|
R6 |
5 |
19 |
74 |
|
Mean |
4.3 |
19.0 |
70.8 |
|
SD |
0.8 |
2.2 |
2.3 |
|
100 |
R1 |
3 |
17 |
64 |
R2 |
4 |
18 |
69 |
|
R3 |
3 |
16 |
68 |
|
R4 |
5 |
17 |
70 |
|
R5 |
4 |
19 |
69 |
|
R6 |
4 |
19 |
66 |
|
Mean |
3.8 |
17.7 |
67.7 |
|
SD |
0.8 |
1.2 |
2.3 |
R1-R6: replicate number
Note: the initial cell density was estimated to be 1 x 104/mL
Table 2 Inhibition of growth
Parameter |
Nominal loading rates (mg/L) |
Sample size |
Mean |
Inhibition (%) |
Area under curve 0 to 72 hours |
Control |
6 |
1350 |
N/A |
100 |
6 |
1268 |
6.1 |
|
Growth rate 0 to 24 hours |
Control |
6 |
0.0604 |
N/A |
100 |
6 |
0.0553 |
8.4 |
|
Growth rate 0 to 48 hours |
Control |
6 |
0.0612 |
N/A |
100 |
6 |
0.0598 |
2.4 |
|
Growth rate 0 to 72 hours |
Control |
6 |
0.0592 |
N/A |
100 |
6 |
0.0585* |
1.1 |
|
Yield |
Control |
6 |
69.8 |
N/A |
10 |
6 |
66.7* |
4.5 |
* : statistically significantly different compared to the control values (2 Sample t-Test;α= 0.05). However this slight deviation is considered as a biological variability of the test system due that this difference was clearly <10%.
Description of key information
effect values for average specific growth rates of Pseudokirchneriella subcapitata, 0-72 h, based on loading rates (OECD 201, EU C.3):
EL50: >100 mg/L, NOELR: ≥ 100 mg/L
Key value for chemical safety assessment
Additional information
EL50 for freshwater algae: > 100 mg/L
NOELR for freshwater algae: ≥ 100 mg/L
The results indicate that the test material is not toxic to algae up to the limits of its solubility and a NOEC and thus a PNEC cannot be determined.
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