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EC number: 939-894-0 | 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:
- 25 February 2013
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Conducted in accordance with ASTM D5191 − 12 Standard Test Method for Vapor Pressure of Petroleum Products (Mini Method). This is a non-GLP method, and is considered to be a K2 study, on the basis that it is an accepted method and describes the vapour pressure derivation for oil based products accurately.
- Qualifier:
- according to guideline
- Guideline:
- other: ASTM D5191 − 12 Standard Test Method for Vapor Pressure of Petroleum Products (Mini Method)
- Deviations:
- not applicable
- Principles of method if other than guideline:
- This test method covers the use of automated vapor pressure instruments to determine the total vapor pressure exerted in vacuum by air-containing, volatile, liquid petroleum products, including automotive spark-ignition fuels with or without oxygenates (see Note 1). This test method is suitable for testing samples with boiling points above 0°C (32°F) that exert a vapor pressure between 7 and 130 kPa (1.0 and 18.6 psi) at 37.8°C (100°F) at a vapor-to-liquid ratio of 4:1.Measurements are made on liquid sample sizes in the range from 1 to 10 mL. No account is made for dissolved water in the sample.
- GLP compliance:
- no
- Type of method:
- effusion method: by loss of weight or by trapping vaporisate
- Temp.:
- 37.8 °C
- Vapour pressure:
- 1.22 kPa
- Remarks on result:
- other: Dry vapour pressure.
- Conclusions:
- The substance demonstrated a dry vapour pressure of 1.22 kPa at 37.8 deg C. This is considered appropriate for hazard assessment purposes, and demonstrates that the substance does not have a high vapour pressure.
- Executive summary:
The substance demonstrated a dry vapour pressure of 1.22 kPa at 37.8 deg C. This is considered appropriate for hazard assessment purposes, and demonstrates that the substance does not have a high vapour pressure.
Reference
Description of key information
Vapour pressure.
Key value for chemical safety assessment
- Vapour pressure:
- 1.22 kPa
- at the temperature of:
- 37.8 °C
Additional information
The substance demonstrated a dry vapour pressure of 1.22 kPa at 37.8 deg C. This is considered appropriate for hazard assessment purposes, and demonstrates that the substance does not have a high vapour pressure. The study was conducted in accordance with ASTM D5191 − 12 Standard Test Method for Vapor Pressure of Petroleum Products (Mini Method). This is a non-GLP method, but is considered to be a K2 study, on the basis that it is an accepted method and describes the vapour pressure derivation for oil based products accurately.
The Klimish rating is considered appropriate in accordance with ANNEX XI-GENERAL RULES FOR ADAPTATION OF THE STANDARD TESTING REGIME SET OUT IN ANNEXES VII TO X, Para 1.1.1 which states that:
1.1.1. Data on physical-chemical properties from experiments not carried out according to GLP or the test methods referred to in Article 13(3)
Data shall be considered to be equivalent to data generated by the corresponding test
methods referred to in Article 13(3) if the following conditions are met:
1) adequacy for the purpose of classification and labelling and/or risk assessment;
2) sufficient documentation is provided to assess the adequacy of the study; and
3) the data are valid for the endpoint being investigated and the study is performed using an acceptable level of quality assurance.
The data presented is considered to fulfil the above, as it is conducted in accordance with recognised non-GLP methods, suitable for the determination of the endpoint specific to the product type, but a suitable qualified external laboratory services provider.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.

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