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EC number: - | 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
Adsorption / desorption
Administrative data
Link to relevant study record(s)
- Endpoint:
- adsorption / desorption: screening
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 29 April 2015 to 03 July 2015
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 121 (Estimation of the Adsorption Coefficient (Koc) on Soil and on Sewage Sludge using High Performance Liquid Chromatography (HPLC))
- Deviations:
- yes
- Remarks:
- test item storage temperature exceeded upper limit on three occasions with no impact on results or integrity of study (see below)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.19 (Estimation of the Adsorption Coefficient (KOC) on Soil and Sewage Sludge Using High Performance Liquid Chromatography (HPLC))
- Deviations:
- yes
- Remarks:
- test item storage temperature exceeded upper limit on three occasions with no impact on results or integrity of study (see below)
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- HPLC estimation method
- Media:
- soil/sewage sludge
- Radiolabelling:
- no
- Test temperature:
- 30 °C
- Details on study design: HPLC method:
- PREPARATION OF REFERENCE STANDARD SOLUTIONS
- Solutions of reference standards were prepared in methanol as shown in Table 3.18 (below).
PREPARATION OF THE DEAD TIME SOLUTION
- The dead time was determined by measuring the retention time of formamide (purity quoted by supplier: 99.94%) at 612 mg/L in methanol:water (55:45 v/v).
PREPARATION OF THE SAMPLE SOLUTION
- Test item (0.1039 g) was diluted to 100 mL with methanol.
DETERMINATION OF RETENTION TIME
- The sample, dead time and reference standard solutions were injected in duplicate using the High Performance Liquid Chromatography (HPLC) parameters shown in the table below.
CALCULATION OF CAPACITY FACTORS
- Capacity factors were determined using the equation k’ = (tr – t0) / t0 where k’ = capacity factor; tr = retention time (min); t0 = dead time (min)
CONSTRUCTION OF THE CALIBRATON CURVE
- A correlation of Log10 k' versus Log10 Koc of the reference items was plotted using linear regression.
- The capacity factors (k') for the reference items were calculated from the retention time data of the dead time and reference item solutions.
- The Log10 Koc values of the reference standards are those quoted in OECD Method 121.
ADSORPTION COEFFICIENT
- The Log10 Koc value was calculated using the equation Log10 Koc = (Log10 k’ – A) / B where Koc = adsorption coefficient; k’ = capacity factor; A = intercept of the calibration curve; B = slope of the calibration curve - Type:
- log Koc
- Value:
- > 4.21 dimensionless
- pH:
- 2.5
- Temp.:
- 30 °C
- Details on results (HPLC method):
- RESULTS
- Typical chromatographs are attached.
- The retention times of the dead time and the retention times, capacity factors and Log10 Koc values for the reference standards are shown in Tables 3.19 and 3.20 (attached).
- The retention times, capacity factors and Log10 Koc values for the sample are shown in Table 3.21 (below). - Validity criteria fulfilled:
- not applicable
- Conclusions:
- The adsorption coefficient of the test item was determined to be > 1.63 x 10E04 with Log10 Koc > 4.21.
- Executive summary:
GUIDELINE
The determination was carried out using the HPLC screening method, designed to be compatible with Method C.19 Adsorption Coefficient of Commission Regulation (EC) No 440/2008 of 30 May 2008 and Method 121 of the OECD Guidelines for Testing of Chemicals, 22 January 2001.
METHODS
The test utilised a High Performance Liquid Chromatograph and a commercially available cyanopropyl reverse phase HPLC column containing lipophilic and polar moieties was used. The dead time was determined by measuring the retention time of formamide (purity quoted by supplier: 99.94%) at 612 mg/L in methanol:water (55:45 v/v). Solutions of reference standards were prepared in methanol and test item (0.1039 g) was diluted to 100 mL with methanol.
RESULTS
The adsorption coefficient of the test item was determined to be > 1.63 x 10E04 with Log10 Koc > 4.21.
Reference
TABLE 3.21 – RETENTION TIMES, CAPACITY FACTOR AND LOG10 Koc VALUES FOR THE SAMPLE
Injection |
Retention time (min) |
Capacity factor (k’) |
Log10 k’ |
Log10 Koc |
1 |
12.400 |
4.73 |
0.675 |
4.21 |
2 |
12.381 |
4.72 |
0.674 |
4.21 |
Mean Log10 Koc: 4.21
Adsorption coefficient: 1.63 x 10E+04
Description of key information
The adsorption coefficient of the test item was determined to be > 1.63 x 10E04 with Log10 Koc > 4.21 (OECD 121 and EU Method C.19).
Key value for chemical safety assessment
- Koc at 20 °C:
- 16 300
Additional information
GUIDELINE
The determination was carried out using the HPLC screening method, designed to be compatible with Method C.19 Adsorption Coefficient of Commission Regulation (EC) No 440/2008 of 30 May 2008 and Method 121 of the OECD Guidelines for Testing of Chemicals, 22 January 2001.
METHODS
The test utilised a High Performance Liquid Chromatograph and a commercially available cyanopropyl reverse phase HPLC column containing lipophilic and polar moieties was used. The dead time was determined by measuring the retention time of formamide (purity quoted by supplier: 99.94%) at 612 mg/L in methanol:water (55:45 v/v). Solutions of reference standards were prepared in methanol and test item (0.1039 g) was diluted to 100 mL with methanol.
RESULTS
The adsorption coefficient of the test item was determined to be > 1.63 x 10E04 with Log10 Koc > 4.21.
[LogKoc: 4.21]
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