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Diss Factsheets
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EC number: 292-053-3 | CAS number: 90530-15-7
- 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
Endpoint summary
Administrative data
Link to relevant study record(s)
Description of key information
The physicochemical and biological data on the test substance suggests that it is readily bioavailable. The test substance would be distributed systemically in the water phase, but would not tend to partition into lipid tissues, it appears to be metabolised and eliminated relatively rapidly.
Key value for chemical safety assessment
- Bioaccumulation potential:
- low bioaccumulation potential
Additional information
A toxicokinetic assessment was conducted based on available physico-chemical properties and toxicological data of the test substance. Data from dermal irritation and skin sensitization indicates relatively good skin penetration even at low concentrations. Examination of the data from the repeat dose oral studies gave an indication of there being good evidence for oral bioavailability by the oral route for the test substance. The high water solubility and low Log Kow suggests relatively high rates of intestinal bioavailability. The biological effects (at dose levels above 300 mg/kg bw/day) following administration of an aqueous solution of test substance confirms the bioavailability. The relatively low volatility suggests a low risk of inhalation exposure. The low vapour pressure suggests low concentrations in air at room temperature which would not be expected to be of any concern. The studies performed and the available physico-chemical data are consistent with an organic molecule with a high bioavailability with no indication or evidence for potential for bioaccumulation. The low Log Kow, the high water solubility and the mammalian toxicity after oral doses at high levels supports the concept of high bioavailability. Low melting point and surface activity would also facilitate high bioavailability. A lack of cumulative toxicity for a chemical with known toxicity supports the concept of rapid elimination of the chemicals. Again, the high water solubility and low Log Kow suggest equilibrium with the water phase in animals, and would not tend to partition onto lipid tissues. The high water solubility would allow rapid excretion in urine. The low toxicity to fish and Daphnia, and the very high water solubility (allowing rapid dilution in the environment) suggest there is not a high risk in environmental exposure scenarios. Based on the above information, the physico-chemical and biological data on the test substance suggests that it is readily bioavailable. The test substance would be distributed systemically in the water phase, but would not tend to partition into lipid tissues, it appears to be metabolised and eliminated relatively rapidly (Esdaile DJ, 2015).
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.