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EC number: 255-707-9 | CAS number: 42204-14-8
- 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
Partition coefficient
Administrative data
Link to relevant study record(s)
- Endpoint:
- partition coefficient
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Justification for type of information:
- REPORTING FORMAT FOR THE ANALOGUE APPROACH
1. HYPOTHESIS FOR THE ANALOGUE APPROACH
Partition coefficient is only relevant for organic substances and as this substance is organometallic this endpoint is not relevant for the inorganic component of the substance. The Kow value for the organic component of the substance is therefore provided to provide information on the partitioning behaviour of this part of the substance.
2. SOURCE AND TARGET CHEMICAL(S) (INCLUDING INFORMATION ON PURITY AND IMPURITIES)
Source: acetic acid
Target: rhodium acetate
3. ANALOGUE APPROACH JUSTIFICATION
This substance is organometallic and therefore partition coefficient is only relevant for the organic component of the substance. The Kow value is therefore read across from acetic acid, the organic component of the substance. This approach is justified as the Kow value is read across from the organic component of the substance and provides sufficient information on the partitioning behaviour of this component. As this is the only component of this substance for which a Kow value is relevant this is considered to be an acceptable approach. - Reason / purpose for cross-reference:
- read-across source
- Type:
- log Pow
- Partition coefficient:
- -0.17
- Temp.:
- 20 °C
- Remarks on result:
- other: temperature assumed
- Conclusions:
- The log kow of acetic acid is -0.17..
- Executive summary:
Hansch et al. (1995) is a reliable, peer-reviewed handbook and so can be considered suitable for use as the key study for this endpoint. The log kow of acetic acid is -0.17.
- Endpoint:
- partition coefficient
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Principles of method if other than guideline:
- The use of secondary sources of data is acceptable when they are based on a critical evaluation of peer-reviewed data and a consequent selection of a reliable and representative value for the property under investigation. The introduction to Exploring QSAR, Hydrophobic, Electronic and Steric Constants states that it is an extensive compilation of published data. Each record is evaluated and the preferred value is identified for each substance. Therefore, although the method used is not known, the values presented here are acceptable as they are from a reliable secondary source of physico-chemical data.
- GLP compliance:
- not specified
- Type of method:
- other: Method details not stated, but result is taken from a reliable, peer-reviewed handbook
- Partition coefficient type:
- octanol-water
- Analytical method:
- not specified
- Type:
- log Pow
- Partition coefficient:
- -0.17
- Temp.:
- 20 °C
- Remarks on result:
- other: temperature assumed
- Conclusions:
- The log kow of acetic acid is -0.17..
- Executive summary:
Hansch et al. (1995) is a reliable, peer-reviewed handbook and so can be considered suitable for use as the key study for this endpoint. The log kow of acetic acid is -0.17.
Referenceopen allclose all
Description of key information
Partition coefficient is not relevant for inorganic substances, but as this substance has an organic component the log Kow for acetic acid, representative of the organic component of rhodium acetate, is read across to rhodium acetate. The log kow of acetic acid is -0.17. This value is read across to the organic component of rhodium acetate.
Key value for chemical safety assessment
- Log Kow (Log Pow):
- -0.17
Additional information
Partition coefficient is not relevant for inorganic substances, but as this substance has an organic component the log Kow for acetic acid, representative of the organic component of rhodium acetate, is read across to rhodium acetate.
Hansch et al. (1995) is a reliable, peer-reviewed handbook and so can be considered suitable for use as the key study for this endpoint. The log kow of acetic acid is -0.17. This value is read across to the organic component of rhodium acetate.
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.