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EC number: 261-351-5 | CAS number: 58594-72-2
- 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
- Study period:
- 26 February to 1 March 1996
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- GLP compliance:
- yes
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No.of test material: ZR023979BEB062
- Expiration date of the lot/batch: not indicated
- Purity test date: not indicated
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: 20°C in the original container
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 0.3, 0.6, 1.2, 2.4, 4.8 mg/l
- Sampling method: Sampling was performed at the beginning and at the end of the test. At the beginning of the test, sampling was done by taking approximately 20 ml of test media out of the additional Erlenmeyer flasks of each concentration and transferring it into an all-glass brown vial. At the end of the test, sampling was done by taking approximately 20 ml of the test media out of all Erlenmeyer flasks.
- Sample storage conditions before analysis: the samples were transferred into the freezer until the moment of analysis - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method:
Two stock solutions were prepared: one of 6 mg imazalil (= stock solution 1) and one of 48 mg imazalil (= stock solution 2). The 6 mg/l concentration was prepared by weighing 0.0061 g imazalil and diluting it to 1000 ml dilution water. The 48 mg/l concentration was prepared by weighing 0.0242 g imazalil and diluting it to 500 ml dilution water. The five concentrations were prepared as follows:
* 0.3 mg/l: 47.5 ml dilution water + 2.5 ml of stock solution 1;
* 0.6 mg/l: 45 ml dilution water + 5 ml of stock solution 1;
* 1.2 mg/l: 40 ml dilution water + 10 ml of stock solution 1;
* 2.4 mg/l: 47.5 ml dilution water + 2.5 ml stock solution 2;
* 4.8 mg/l: 45 ml dilution water + 5 ml of stock solution 2;
* control: 50 ml dilution water
- Controls: yes - Test organisms (species):
- Pseudokirchneriella subcapitata (previous names: Raphidocelis subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- TEST ORGANISM
- Common name: algae
- Strain: CCAP 278/4
- Source (laboratory, culture collection): Culture Collection of Algae and Protozoa (CCAP), UK
- Method of cultivation: The algae were cultured under sterile conditions at the laboratory for several weeks in Bold's Basal Medium
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Hardness:
- 0.6 mmol/L
- Test temperature:
- 25+-1°C
- pH:
- 7.27 - 8.88
- Dissolved oxygen:
- not indicated
- Salinity:
- not applicable
- Conductivity:
- not applicable
- Nominal and measured concentrations:
- Nominal concentrations: 0.3, 0.6, 1.2, 2.4, 4.8 mg/l
Mean measured concentrations: 0.234, 0.457, 0.940, 1.485, 3.303 mg/l - Details on test conditions:
- TEST SYSTEM
- Test vessel: Erlenmeyer flasks
- Type (delete if not applicable): open / closed - Material, size, headspace, fill volume: all-glass Erlenmeyer flasks of 100 ml, marked at 50 ml
- Initial cells density: 10E+04 cells/ml
- Control end cells density: 5.77E+05 cells/ml
GROWTH MEDIUM
- Standard medium used: yes
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water:
* NH4Cl 15 mg/l
* MgCl2.6H2O 12 mg/l
* CaCl2.2H2O 18 mg/l
* MgSO4.7H2O 15 mg/l
* KH2PO4 1.6 mg/l
* FeCl3.6H2O 80 µg/l
* K2-EDTA.2H2O 109.6 µg/l
* H3BO3 185 µg/l
* MnCl2.4H2O 415 µg/l
* ZnCl2 3 µg/l
* CoCl2.6H2O 0.01 µg/l
* CuCl2.2H2O 0.01 µg/l
* Na2MoO4.2H2O 7 µg/l
* NaHCO3 50 mg/l
OTHER TEST CONDITIONS
- Sterile test conditions: yes
- Photoperiod: continuous illumination
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
- Determination of cell concentrations: Neubauer counting chamber under a microscope (model BHTU-112, OLYMPUS)
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2
- Range finding study: yes
- Test concentrations: 0.7, 1.4, 2.8, 5.6, 11.2 mg/l (based on results from a previous study indicating that the EC50-72h was situated in a range of 1-10 mg/l)
- Results used to determine the conditions for the definitive study: yes - Reference substance (positive control):
- no
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 1.73 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 1.2 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.6 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.:
- 0.457 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Details on results:
- - Observation of abnormalities (for algal test): none indicated
- Unusual cell shape: none indicated
- Validity criteria fulfilled:
- yes
- Conclusions:
- A 72h growth inhibition test with the unicellular green alga Pseudokirchneriella subcapitata was performed with the test substance Imazalil according to the OECD guideline 201. The EC50 72h calculated on the basis of the measured concentrations was 1.20 mg imazalil /L. The NOEC after 72 hours of exposure was 0.457 mg imazalil /L as measured concentration. The results of the test can be considered reliable without restrictions.
- 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:
- Data from the related substance imazalil base is used to cover this endpoint. The justification for read across is attached in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across source
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 1.6 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Remarks:
- imazalil sulfate (recalculated from imazalil concentration)
- Basis for effect:
- growth rate
- Key result
- Duration:
- 72 d
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.61 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Remarks:
- imazalil sulfate (recalculated from imazalil concentration)
- Basis for effect:
- growth rate
Referenceopen allclose all
Description of key information
The study of Van Ginneken (1996), investigating the acute toxicity of Imazalil to algae according to OECD guideline 201, was considered as the key study for endpoint coverage. The 72h NOEC and 72h EC50 for growth rate were determined to be 0.457 mg/L and 1.2 mg/L respectively which corresponds to 0.61 and 1.60 mg imazalil sulphate /L. The substance can be considered as harmful to algae.
Key value for chemical safety assessment
- EC50 for freshwater algae:
- 1.6 mg/L
- EC10 or NOEC for freshwater algae:
- 0.61 mg/L
Additional information
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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