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Diss Factsheets
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EC number: 946-958-1 | 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:
- The study was conducted between 7 May 2014 and 18 July 2014.
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 104 (Vapour Pressure Curve)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.4 (Vapour Pressure)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 830.7950 (Vapor Pressure)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- gas saturation method
- Specific details on test material used for the study:
- Lot No.: VE00313054
Aspect: Yellow viscous liquid - Temp.:
- 20 °C
- Vapour pressure:
- ca. 0.17 Pa
- Remarks on result:
- other: Aurantiol Pure is a complex reaction mixture. Hydroxycitronellal Synthetic and Methyl Anthranilate are the often most volatile constituents in the reaction mixture and do therefore govern the overall vapour pressure.
- Conclusions:
- Aurantiol Pure is a complex reaction mixture. Hydroxycitronellal Synthetic and Methyl Anthranilate are the often most volatile constituents in the reaction mixture and do therefore govern the overall vapour pressure.
The partial vapour pressures of Hydroxycitronellal Synthetic and Methyl Anthranilate Extra at 20°C were calculated from the average headspace concentration.
The partial vapour pressures are added to obtain the total vapour pressure of Aurantiol Pure.
Therefore the vapour pressure of Aurantiol Pure is 0.17 Pa at 20°C. - Executive summary:
The vapour pressure of Aurantiol Pure was determined using the gas saturation method according to Method A4 Vapour Pressure of Commission Regulation (EC) No 440/2008 and Method 104 of the OECD Guidelines for Testing of Chemicals. The vapour pressure of Aurantiol Pure is 0.17 Pa at 20°C.
Reference
Description of key information
The vapour pressure of Aurantiol Pure has been determined to be 0.17 Pa at 20 °C, using the Gas Saturation method designed to be compatible with Method A4 Vapour Pressure of Commission Regulation (EC) No 440/2008 of 30 May 2008 and Method 104 of the OECD Guidelines for Testing of Chemicals, 23 March 2006.
Key value for chemical safety assessment
- Vapour pressure:
- 0.17 Pa
- at the temperature of:
- 20 °C
Additional information
Aurantiol Pure is a complex reaction mixture. Hydroxycitronellal Synthetic and Methyl Anthranilate are the most volatile constituents in the reaction mixture and therefore govern the overall vapour pressure. The partial vapour pressures of Hydroxycitronellal Synthetic and Methyl Anthranilate Extra at 20°C were calculated from the average headspace concentration (0.06Pa and 0.11Pa respectively) and added to obtain the total vapour pressure of Aurantiol Pure.
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