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EC number: 300-326-6 | CAS number: 93925-25-8
- 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
- Study period:
- Between 17 October 2011 and 25 October 2011.
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Valid and conclusive guideline study under GLP
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.4 (Vapour Pressure)
- Version / remarks:
- Commission Regulation (EC) No 440/2008 of 30 May 2008
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- Department of Health of Government of the U.K., inspection 19-21 July 2011
- Type of method:
- effusion method: vapour pressure balance
- Temp.:
- 25 °C
- Vapour pressure:
- 0 Pa
- Remarks on result:
- other: Mean of 9 measurements between 50 to 60 °C
- Transition / decomposition:
- no
- Conclusions:
- Vapour pressure 0.00043 Pa at 25 ºC (irrelevantly low volatilization)
- Executive summary:
The vapour pressure of the test item was determined in a GLP-compliant study using the effusion method (vapour pressure balance) according to the EU A.4 (2008) protocol. The experiment is deemed valid, conclusive and thus suitable for assessment without restrictions.
A sequence of runs was started after a sample of test item had been under vacuum for approximately 22¾ h. Temperature and pressure readings were taken between 50 and 60 ºC with a 1 h dwell at 50 ºC between runs. Linear regression analysis was used to conclude on the vapour pressure at 25 °C. Nine of the ten runs were evaluable as equilibration with regard to the vapour pressure was not reached in the first run. No decomposition was observed.
In conclusion the vapour pressure was found to be 0.00043 Pa at 25 ºC, which indicates irrelevantly low volatilization.
Reference
Table 1: Summary of results
Run |
Log Vp at 25 ºC [Pa] |
Slope ± Standard deviation |
Intercept ± Standard deviation |
2 |
-3.170 |
-4494.231±132.693 |
1 1.904±0.404 |
3 |
-3.297 |
-4772.984±169.001 |
12.712±0.515 |
4 |
-3.373 |
-4896.609±190.543 |
13.050±0.581 |
5 |
-3.515 |
-5302.897±171.244 |
14.271±0.522 |
6 |
-3.427 |
-4991.940±141.453 |
13.316±0.431 |
7 |
-3.424 |
-5060.034±156.595 |
13.547±0.477 |
8 |
-3.282 |
-4605.359±446.656 |
12.165±1.361 |
9 |
-3.207 |
-4376.681±496.267 |
1 1.472±1.51 3 |
10 |
-3.599 |
-551 3.707±261 .I36 |
14.894±0.796 |
Mean |
-3.366 |
A total of ten runs were completed for the main sequence. Equilibrium with regard to vapour pressure was assessed to have been reached over the final nine runs. Thus the final nine runs have been used to calculate the definitive vapour pressure value for the test item.
The test item did not change in appearance under the conditions used in the determination.
Description of key information
Irrelevantly low volatilization (EU Method A.4)
Key value for chemical safety assessment
- Vapour pressure:
- 0 Pa
- at the temperature of:
- 25 °C
Additional information
The vapour pressure was determined in a GLP-compliant study (Tremain & Atwal 2011, Harlan Report no. 41103264) using the effusion method (vapour pressure balance) according to the EU A.4 (2008) protocol. The experiment is deemed valid, conclusive and thus suitable for assessment without restrictions.
Measurements were made at several temperatures from 50 to 60 °C and linear regression analysis was used to conclude on the vapour pressure at 25 °C. No decomposition was observed.
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