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EC number: 469-910-7 | CAS number: 847842-48-2
- 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)
Description of key information
A water solubility study carried out on the reference substance (White & Mullee, 2007AG) gave a determination of 5.14 g/L of solution at 20.0 ± 0.5°C.
A second study carried out on an analogue substance (White & Woolley, 2007AH) gave a determination of 70.3 g/L of solution at 20.0 ± 0.5°C.
An additional study carried out on an analogue substance (Sydney, 1997) gave a determination as follows:
17.4 ± 0.4 g/L in pH 5.0 buffer
25.3 ± 0.2 g/L in pH 7.0 buffer
22.4 ± 1.1 g/L in pH 9.0 buffer
Key value for chemical safety assessment
- Water solubility:
- 5.14 g/L
- at the temperature of:
- 20 °C
Additional information
A water solubility study carried out on the reference substance (White & Mullee, 2007AG) gave a determination of 5.14 g/L of solution at 20.0 ± 0.5°C.
A second study carried out on an analogue substance (White & Woolley, 2007AH) gave a determination of 70.3 g/L of solution at 20.0 ± 0.5°C.
Both 2007 studies were conducted to the same standards and therefore considered to be reliable whilst the third study was conducted to US FDA Environmental Assessment guidelines. However as the first study (White & Mullee, 2007AG) was carried out
on the substance of interest this was considered to be the key study for the purposes of this assessment.
White & Mullee 2007:
This study was performed on Abacavir Glutarate.The determination was carried out using the flask method, Method A6 of
Commission Directive 92/69/EEC (which constitutes Annex V of Council Directive 67/548/EEC).
The water solubility of the test material has been determined to be 5.14 g/L of solution at 20.0 ± 0.5°C.
White & Woolley 2007: This study was performed on Abacavir Hemisulphate and has been used for read-across purposes.
The water solubility and partition coefficient ofthe test material have been determined using the flask method, Method A6 of Commission Directive 92/69/EEC.
The water solubility of the test material has been determined to be 70.3 g/L of solution at 20.0 ± 0.5°C.
Sydney 1997:
This study was performed on Abacavir Succinate and has been used for read-across purposes. The solubilities of the test material were determined by the flask shake method according to the US FDA Environmental Assessment Technical Assistance Handbook (March 1987).
The aqueous solubility of the test material at 20°C is:
17.4 ± 0.4 g/L in pH 5.0 buffer
25.3 ± 0.2 g/L in pH 7.0 buffer
22.4 ± 1.1 g/L in pH 9.0 buffer
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