Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 947-162-7 | 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
Water solubility
Administrative data
Link to relevant study record(s)
- Endpoint:
- water solubility
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 105 (Water Solubility)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.6 (Water Solubility)
- GLP compliance:
- yes
- Type of method:
- flask method
- Water solubility:
- 2.18 g/L
- Conc. based on:
- test mat.
- Loading of aqueous phase:
- 10 g/L
- Incubation duration:
- 24 h
- Temp.:
- 20 °C
- pH:
- 9.4
- Conclusions:
- The water solubility of the test item in demineralized water at 20 °C was determined to be 2.18 g/L.
- Executive summary:
The water solubility of the test item was determined according to OECD Guideline 105.
In a preliminary test, the water solubility of the test item was found to be > 10^-2 g/L (approximately 640 mg/L). Therefore, the shake flask method was chosen for the determination of the water solubility. For the main test, a quantity of the test item necessary for saturation is dissolved in demineralized water. The vessels are stoppered and stirred on a magnetic stirrer for 24 h, 48 h and 72 h at 30 °C in a temperature controlled water bath. Following this procedure, the temperature is reduced to 20 °C and is kept in the temperature controlled water bath for another 24 h. After phase separation by filtration with a disposable syringe filter and/or centrifugation (20 minutes, 11000 rpm, 20 °C), the concentration of the test item in aqueous test solutions was determined by HPLC-analysis with UV-detection.
The test item is described as a mixture of two main constituents. The HPLC-UV chromatogram of the test item showed two peaks representing the two main constituents: tetraphenylphosphanium and phenol (determined as sum of phenolate and free phenol). Therefore, individual water solubility values of tetraphenylphosphanium and phenol were determined by external calibration using certified calibration substances. The water solubility of the test item was calculated as sum of both values.
Water solubility of the test item was determined to be 2.18 g/L (at 20 °C). The relative standard deviation between the single determinations was < 15 %. The validity criteria have been met.
Reference
The relative standard deviation between the single determinations is < 15 %.
The validity criteria have therefore been met.
Description of key information
The water solubility of the test item in demineralized water at 20 °C was determined to be 2.18 g/L.
Key value for chemical safety assessment
- Water solubility:
- 2.18 g/L
- at the temperature of:
- 20 °C
Additional information
The water solubility of the test item was determined according to OECD Guideline 105.
In a preliminary test, the water solubility of the test item was found to be > 10^-2 g/L (approximately 640 mg/L). Therefore, the shake flask method was chosen for the determination of the water solubility. For the main test, a quantity of the test item necessary for saturation is dissolved in demineralized water. The vessels are stoppered and stirred on a magnetic stirrer for 24 h, 48 h and 72 h at 30 °C in a temperature controlled water bath. Following this procedure, the temperature is reduced to 20 °C and is kept in the temperature controlled water bath for another 24 h. After phase separation by filtration with a disposable syringe filter and/or centrifugation (20 minutes, 11000 rpm, 20 °C), the concentration of the test item in aqueous test solutions was determined by HPLC-analysis with UV-detection.
The test item is described as a mixture of two main constituents. The HPLC-UV chromatogram of the test item showed two peaks representing the two main constituents: tetraphenylphosphanium and phenol (determined as sum of phenolate and free phenol). Therefore, individual water solubility values of tetraphenylphosphanium and phenol were determined by external calibration using certified calibration substances. The water solubility of the test item was calculated as sum of both values.
Water solubility of the test item was determined to be 2.18 g/L (at 20 °C). The relative standard deviation between the single determinations was < 15 %. The validity criteria have been met.
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.