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EC number: 429-580-7 | 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:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Justification for type of information:
- ANALOGUE APPROACH JUSTIFICATION
Please refer to the attached read across justification in section 13 - Reason / purpose for cross-reference:
- read-across source
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Key result
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- from 2000-08-18 to 2000-09-25
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Freshwater Alga and Cyanobacteria, Growth Inhibition Test)
- Version / remarks:
- 2006
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.3 (Algal Inhibition test)
- Version / remarks:
- EEC, Directive 92/69/1992
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- no
- Details on sampling:
- - Sampling: after 24, 48, or 72 hours
- Vehicle:
- no
- Details on test solutions:
- The test medium (reconstituted water and test item) was freshly prepared. The calibrated flask with test item and vehicle, reconstituted water, was treated in an ultrasound bath for 1 hour. Subsequently, the preparation was stirred with a magnetic stirrer for further 23 hours. Afterwards, the preparation was filtered through a filter funnel with a pore size of 10 - 16 µm. The filtrate was used for the study.
- Test organisms (species):
- Desmodesmus subspicatus (previous name: Scenedesmus subspicatus)
- Details on test organisms:
- TEST ORGANISM
- Common name: green unicellular algae
- Strain: SAG 86.81
- Source (laboratory, culture collection): "Sammlung von Algenkulturen, Pflanzenphysiologisches Institut der Universitat Gottingen"
- Method of cultivation: Prior to start the study, the algae were grown in reconstituted water as preculture and the growth rate was determined.
ACCLIMATION
- Acclimation period: none
- Culturing media and conditions (same as test or not):the same - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 72 h
- Hardness:
- 250 mg CaCO3
- Test temperature:
- 22 - 23 °C
- pH:
- 7.81 - 9.74
- Nominal and measured concentrations:
- Nominal concentration of 100 mg/L (limit test); due to very the low water solubility and the fact that the study was a limit test, no further analysis was initiated.
- Details on test conditions:
- TEST SYSTEM
- Test vessel: Erlenmeyer flasks
- Type: open - completely sealed with sterilized stoppers
- Material, size, headspace, fill volume: glass, 300 mL, 100 mL fill volume
- Aeration: none
- Initial cells density: 10000 algae cells/mL
- Control end cells density: 1188540 cells/mL
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
GROWTH MEDIUM
- Standard medium used: yes, reconstitution water prepared according to the guideline
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: same as the growth medium
OTHER TEST CONDITIONS
- Sterile test conditions: no
- Adjustment of pH: no
- Photoperiod: continuously illuminated
- Light intensity and quality: 7500 to 9500 Lux
EFFECT PARAMETERS MEASURED
- Determination of cell concentrations:The algae cell densities were determined with an electronic particle counter (Coulter, Z2).
TEST CONCENTRATIONS
- Justification for using less concentrations than requested by guideline: In a pretest under static conditions, inhibition of the growth rate of the algae, Desmodesmus subspicatus, was not observed at a concentration of 100 mg/L nominally. - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Key result
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Results with reference substance (positive control):
- Regularly, a positive control test to check the test system is carried out with potassium dichromate.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The test item was tested to Desmodesmus subspicatus in an open static test system according to OECD 201 (1984). Under the given conditions of this study the 72-h ErC50 value and the 72-h NOEC were determined to be > 100 mg/L.
- Executive summary:
The influence of the test substance on the growth and growth rate of the green algae species Desmodesmus subspicatus was tested according to OECD 201 (1984) under GLP conditions. The study design included one control and one test item group with three replicates, each containing about 100 mL reconstituted water or test medium and 10000 cells/mL at the start of the experimental phase. The algae were exposed to a filtrate of nominal 100 mg/L and the study was performed as a limit test in an open static test system. The analysis of the saturated aqueous preparation revealed that the water solubility of the test substance in reconstituted water was < 0.005 mg/L and could not be determined analytically. The test material concentration in the aqueous medium could not be quantified since it was below the level of detection. Regularly, a positive control test to check the test system is carried out with potassium dichromate. The validity criteria of the test were met. Under the given conditions of this study the 72-h ErC50 value and the 72-h NOEC were determined to be > 100 mg/L.
Referenceopen allclose all
Table 1: Cell density
|
Cell density per mL |
Growth inhibition (0 - 72 hours) |
|||||
nominal |
|
0 hour |
24 hours |
48 hours |
72 hours |
1a |
1µt |
0 |
|
10,000 |
51,030 |
241,791 |
1,230,633 |
|
|
|
10,000 |
54,927 |
257,040 |
1,228,527 |
|
|
|
|
10,000 |
52,740 |
242,420 |
1,106,460 |
|
|
|
|
mean |
10,000 |
52,899 |
247,084 |
1,188,540 |
|
|
100 |
|
10,000 |
59,130 |
319,209 |
1,268,460 |
|
|
|
10,000 |
58,473 |
333,251 |
1,280,610 |
|
|
|
|
10,000 |
60,210 |
324,411 |
1,260,117 |
|
|
|
|
mean |
10,000 |
59,271 |
325,624 |
1,269,729 |
|
|
Inhibition la |
|
-14.9 |
-30.3 |
-11.3 |
-144 |
-1.4 |
Ia
= inhibition of cell growth in percent
Iµt
= Inhibition of growth rate in percent
-Ia
= The growth of the algae was better in the test medium than in the
control group.
A
dose group with nominal 100 mg/L of the test item (maximal water
solubility < 0 005 mg/L) revealed no aquatic toxicity in this test
system.
An
aqueous solution of nominal 100 mg/L of the test item revealed no effect
for Desmodesmus subspicatus. The EC50 exceeded the maximal
water solubility (< 0.005 mg/L) of the test material and. thus, could
not be determined in this test.
The
following ECx values and no effect concentration for
Desmodesmus subspicatus were determined:
72
h EbC50 = > 0.005 mg/L (nominal > 100 mg/L)
72
h ErC50 = > 0.005 mg/L (nominal > 100 mg/L)
NOEC = > 0 005 mg/L (nominal > 100 mg/L)
Description of key information
The read-across substance was tested to Desmodesmus subspicatus in an open static test system according to OECD 201 (1984). Under the given conditions of this study (reference 6.1.5-1) the 72-h ErC50 value and the 72-h NOEC were determined to be > 100 mg/L.
Key value for chemical safety assessment
Additional information
For this endpoint a one-to-one read across was performed to a chemical similar compound of the same chemical class with a comparable physicochemical profile and similar data in biological relevant assays. The study was performed according to GLP and the methods applied are fully compliant with OECD TG 201.
The influence of the test substance on the growth and growth rate of the green algae species Desmodesmus subspicatus was tested according to OECD 201 (1984) under GLP conditions. The study design included one control and one test item group with three replicates, each containing about 100 mL reconstituted water or test medium and 10000 cells/mL at the start of the experimental phase. The algae were exposed to a filtrate of nominal 100 mg/L and the study was performed as a limit test in an open static test system. The analysis of the saturated aqueous preparation revealed that the water solubility of the test substance in reconstituted water was < 0.005 mg/L and could not be determined analytically. The test material concentration in the aqueous medium could not be quantified since it was below the level of detection. Regularly, a positive control test to check the test system is carried out with potassium dichromate. The validity criteria of the test were met. Under the given conditions of this study the 72-h ErC50 value and the 72-h NOEC were determined to be > 100 mg/L (reference 6.1.5-1).
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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