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EC number: 701-359-2 | 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

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:
- From December 10, 2011 to March 28, 2012
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.4 (Vapour Pressure)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 104 (Vapour Pressure Curve)
- Deviations:
- no
- GLP compliance:
- yes
- Type of method:
- effusion method: isothermal thermogravimetry
- Specific details on test material used for the study:
- Batch: HTIF11021
- Key result
- Temp.:
- 20 °C
- Vapour pressure:
- < 0 Pa
- Key result
- Temp.:
- 25 °C
- Vapour pressure:
- < 0 Pa
- Conclusions:
- Under the study conditions, the vapour pressure of the test substance was < 1.3E-08 Pa at 20°C and < 6.5E-08 Pa at 25°C.
- Executive summary:
A study was conducted to determine the vapour pressure of the test substance according to EU Method A.4 (Vapour pressure) and OECD guideline 104 (Vapour pressure curve). The vapour pressure of the test substance (PT) was determined by the isothermal thermogravimetric effusion method. The method is validated in the range 10E-08 - 10E03 Pa using a set of five reference substances with known vapour pressures. The validity of the method was verified maximum one month before this study using hexachlorobenzene (>99%, Fluka Chemie, Buchs, Switzerland) as reference control substance. The logarithm of the evaporation rate at 20°C (log vT, 20) deviated < 10% from the average value obtained during the validation test. From this, it was possible to apply the constants obtained with the validation test for the determination of the vapour pressure of the test substance. Under the study conditions, the vapour pressure of the test substance was < 1.3E-08 Pa at 20°C and < 6.5E-08 Pa at 25°C (Oudhoff, 2012).
Reference
The vapour pressure is a function of the temperature and is specified in Pascal (Pa) or in mm Hg.
Equations:
-Evaporation rate (νT) = delta m/F*t (g/cm2/h) (where: delta m = weight loss of the test substance, F = surface of the sample late, and t = elapsed time for the weight loss).
-Vapour pressure equation (logPT) = c logvT + d (where: c and d = constants specific for the experiment arrangement).
-Vapour pressure regression curve (PT) = a 1/T + b (where T = temperature (K), a = slope (K), and b = intercept).
Results:
The weight loss of the test substance at 210°C, 220°C, 230°C and 240°C was lower than the weight loss of benzo(ghi)perylene at the same temperatures.
Vapour pressure values:
20°C | 20°C | 25°C | 25°C | |
Pa | mm Hg | Pa | mmHg | |
Test substance | <1.3E-08 | <1.0E-10 | <6.5E-08 | <4.8E-10 |
Description of key information
The vapour pressure was determined according to OECD Guideline 104 and EU Method A.4 (Oudhoff, 2012).
Key value for chemical safety assessment
- Vapour pressure:
- 0 Pa
- at the temperature of:
- 20 °C
Additional information
The vapour pressure of the substance was < 1.3E-08 Pa at 20°C and < 6.5E-08 Pa at 25°C
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.
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