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Diss Factsheets
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EC number: 947-340-4 | 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
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:
- 2012-01-12 - 2012-12-12
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The GLP study was conducted according to an internationally accepted guideline. All study parameters are given in detail.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 117 (Partition Coefficient (n-octanol / water), HPLC Method)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- HPLC method
- Partition coefficient type:
- octanol-water
- Analytical method:
- high-performance liquid chromatography
- Key result
- Type:
- log Pow
- Partition coefficient:
- > 0.3 - <= 3.324
- Temp.:
- 25 °C
- pH:
- 5.5
- Conclusions:
- It is concluded that the log POW of the test item Ukanol FR 70 is the range from < 0.3 to 3.324.
- Executive summary:
This study was performed in order to estimate the distribution coefficient log Pow of Ukanol FR 70 using HPLC following OECD guideline 117.
The study was performed using a HPLC with a C18 column. Seven reference items with different retention times were used to produce a calibration curve, since retention time on hydrophobic columns and POW are correlated. The reference items were chosen on behalf of the calculated log POW provided by the sponsor. First, a solution of the reference items was analysed with HPLC, then a solution of the test item; and finally again the solution with the reference items. Each analysis was performed three times, totalling to nine runs. For each reference item, the capacity factor K was calculated from the retention time of thio urea and the retention time of the respective reference item. A calibration function (log K versus log POW, linear fit) was determined using the literature values for Log POW of the reference items and the retention times in the six determinations.
Variations in the retention times of reference items and test item were very small. Therefore a stable configuration of the HPLC-column could be assumed. The correlation log K/Log Pow was good: the coefficient of determination r2 was calculated with 0.9859. This value was considered as sufficiently high to use the calibration function for the determination of the log POW of the test item Ukanol FR 70. The calculated log POW of the first peak of the test item solution were underneath the range of the Log POW of the reference items and therefore stated as < 0.3.
As peaks 2, 6, 7, 8 and 11 - 13 showed relative areas < 5%, they were considered as minor peaks. Although area is not necessarily correlated to the absolute concentration, if a UV detector is used, it is considered that the test item Ukanol FR 70 consists mainly of peaks 1, 3 - 5 and 9 - 10. Thus it is concluded that the log POW of the test item Ukanol FR 70 is the range from <0.3 - 3.324.
Reference
Description of key information
The study was performed in order to estimate the distribution coefficient log Pow of Ukanol FR 70 using HPLC following OECD guideline 117.
The log POW of the test item Ukanol FR 70 was estimated to be in the range from < 0.3 to 3.324.
Key value for chemical safety assessment
- Log Kow (Log Pow):
- 3.324
- at the temperature of:
- 25 °C
Additional information
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