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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
Partition coefficient
Administrative data
Link to relevant study record(s)
- Endpoint:
- partition coefficient
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 11 February - 9 April 2002
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 117 (Partition Coefficient (n-octanol / water), HPLC Method)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.8 (Partition Coefficient - HPLC Method)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- HPLC method
- Partition coefficient type:
- octanol-water
- Specific details on test material used for the study:
- - Batch n°: ZR027180PUG231
- Analytical purity: 99.3%
- Expiration date: 9 November 2006
- Storage condition: at room temperature, 10 to 30°C - Key result
- Type:
- log Pow
- Partition coefficient:
- 3.31
- Temp.:
- 20 °C
- pH:
- 7
- Remarks on result:
- other: No temperature or pH value were reported but based on the use of references a standard temperature of 20°C and pH7 are assumed
- Remarks:
- The mobile phase for elution was MeOH 0.01M pH4 citrate buffer 75:25
- Details on results:
- The compound Imazalil 75SP eluted as a single peak with a retention time which was within the range of retention times of the calibration substances. Therefore the results of the estimation may be expected to be realistic, as the results were calculated by interpolation rather than extrapolation. It was possible to establish the calibration line with six different calibration compounds, three eluting before the test compound and three after.
There were only minimal differences between the replicates of retention times for each of the calibration and test substances, and between the two injection sequences. The resultant calculated values differed only to a small extent, therefore the results may be considered as acceptable for regulatory purposes.
The partition coefficient of Imazalil 75SP (Product ZR027180) was successfully evaluated using the HPLC simulation technique with a mobile phase of MeOH 0.01M pH4 citrate buffer 75:25. The test substance eluted as a single component exhibiting a retention time corresponding to a log Pow value of +3.31 and which was within a 95% confidence range of +3.2 to +3.4. - Conclusions:
- The partition coefficient of the test substance was determined to be log Pow value of +3.31, and which was within a 95% confidence range of +3.2 to + 3.4.
Reference
Description of key information
Based on a key study (K1, Bates, 2002) using the HPLC method according to EU method A.8 and OECD guideline 117, the partition coefficient (log Pow) of the test item was determined to be 3.31.
Key value for chemical safety assessment
- Log Kow (Log Pow):
- 3.31
- at the temperature of:
- 20 °C
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.