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EC number: 204-279-1 | CAS number: 118-82-1
- 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
Vapour pressure
Administrative data
Link to relevant study record(s)
- Endpoint:
- vapour pressure
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline Study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 104 (Vapour Pressure Curve)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- gas saturation method
- Temp.:
- 25 °C
- Vapour pressure:
- 0 Pa
- Executive summary:
The gas saturation method as outlined in the OECD guideline 104 was used to ascertain the vapor pressure of the test material. The vapor pressure of the test substance at 25°C was estimated by extrapolation using the trendline that described the vapor pressure as function of T. The vapor pressure at 25°C is calculated to be 2.9 x 10-6 Pa.
- Endpoint:
- vapour pressure
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: EU method and GLP study.
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.4 (Vapour Pressure)
- Deviations:
- no
- GLP compliance:
- yes
- Type of method:
- other: balance method
- Temp.:
- 25 °C
- Vapour pressure:
- 0 Pa
- Conclusions:
- Vapour pressure at 25 ºC = 6 x 10 -8 Pa
- Executive summary:
The vapour pressure was determined according to EU method A.4 (balance method) to be 6 x 10 -8 Pa at 25 ºC
Referenceopen allclose all
Results of the gas saturation experiments at 50°C
The experiments at 50°C were performed using three flow rates (2.00 L/min, 1.00 L/min and 0.20 L/min) during approximately 12 (experiment no.1) or 7 days (experiment no.3). Flow rate, pressure and temperature were checked and recorded 5 (no. 1) or 3 (no. 3) times in that period. The collected vapor was desorbed from the traps with acetonitrile. The amount of test substance in the eluent was determined by GC method.
The results of the measurements are summarized in the following table:
The results of the saturation experiments with the test substance at 50°C |
||||||
Channel number |
Temperature (°C) |
Flow (L/min) |
Time (min) |
PS(Pa) |
Wg(mg) |
P (Pa) |
1 |
46.0 |
2.015 |
9825 |
2.16 x 105 |
34.917 |
2.01 x 10-5 |
2 |
- |
- |
- |
- |
- |
- |
3 |
46.6 |
0.9968 |
17085 |
1.14 x 105 |
49.081 |
1.73 x 10-5 |
* At flow rate of 1.00 L/min there was a leakage in the test equipment. Therefore, only the results of experiment 1 and 3 were used for the calculation.
Results of the gas saturation experiments at 40°C
The experiments at 40°C were performed using three flow rates (2.00 L/min, 1.00 L/min and 0.20 L/min) during approximately 13 days. Flow rate, pressure and temperature were checked and recorded 9 times in that period. The collected vapor was desorbed from the traps with acetonitrile. The amount of test substance in the eluent was determined by GC method.
The results of the measurements are summarized in the following table:
The results of the saturation experiments with the test substance at 40°C |
||||||
Channel number |
Temperature (°C) |
Flow (L/min) |
Time (min) |
PS(Pa) |
Wg(mg) |
P (Pa) |
1 |
- |
- |
- |
- |
- |
- |
2 |
- |
- |
- |
- |
- |
- |
3 |
39.2 |
0.9968 |
18345 |
1.11 x 105 |
17.848 |
5.71 x 10-6 |
* At flow rate of 2.00 and 1.00 L/min there was a leakage in the test equipment. Therefore, only the results of experiment 3 was used for the calculation.
Results of the gas saturation experiments at 30°C
The experiments at 30°C were performed using three flow rates (2.00 L/min, 1.00 L/min and 0.20 L/min) during approximately 7 days. Flow rate, pressure and temperature were checked and recorded 4 times in that period. The collected vapor was desorbed from the traps with acetonitrile. The amount of test substance in the eluent was determined by GC method.
The results of the measurements are summarized in the following table:
The results of the saturation experiments with the test substance at 30°C |
||||||
Channel number |
Temperature (°C) |
Flow (L/min) |
Time (min) |
PS(Pa) |
Wg(mg) |
P (Pa) |
1 |
29.4 |
2.015 |
9910 |
1.95 x 105 |
9.778 |
5.04 x 10-6 |
2 |
- |
- |
- |
- |
- |
- |
3 |
29.4 |
0.9968 |
9910 |
1.08 x 105 |
7.029 |
4.04 x 10-6 |
* At flow rate of 1.00 L/min there was a leakage in the test equipment. Therefore, only the results of experiments 1 and 3 were used for the calculation.
Conclusion of the gas saturation experiments
In a Clausius-Clapeyron plot, the logarithm of the vapor pressure is plotted as a function of the inverse temperature. The vapor pressure of the test substance at 25°C can be estimated by extrapolation using the trendline that describes the vapor pressure as function of T. The vapor pressure at 25°C is calculated to be 2.9 x 10-6 Pa.
Vapour pressure at 25 ºC = 6 x 10 -8 Pa
Description of key information
Key study: experimental results: GLP study. The vapour pressure was determined according to EU method A.4 to be 6 x 10 -8 Pa at 25 ºC
Key value for chemical safety assessment
- Vapour pressure:
- 0 Pa
- at the temperature of:
- 25 °C
Additional information
Key study: experimental results: GLP study. The vapour pressure was determined according to EU method A.4 to be 6 x 10 -8 Pa at 25 ºC
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