Registration Dossier
Registration Dossier
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Diss Factsheets
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EC number: 473-820-3 | 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
Endpoint summary
Administrative data
Link to relevant study record(s)
Description of key information
A literature-based toxicokinetic assessment was carried out.
Key value for chemical safety assessment
Additional information
The data presented in this dossier only allows a qualitative assessment of the toxicokinetic behaviour of the substance for registration. The data was awarded a reliability score of 4 in accordance with the criteria for assessing data quality set forth by Klimisch et al. (1997). However, a couple of significant conclusions can be made.
Hyperform™ HPN-20E has a molecular weight of 210 g/mol. It is a poorly soluble solid (solubility 296 mg/L), with over 87 % of the particles being >100 µm in size. The melting point is > 360 °C and the substance has a very low vapour pressure. The logPow is -2.56. The substance appears stable in solution at pH 4, 7 and 9. The substance is essentially non-toxic.
Absorption
The substance is poorly soluble in water and even less soluble in lipids. Thus it is unlikely to be absorbed orally or dermally. Although a poorly soluble particulate, the particle size is such that very little is likely to be inhaled and retained.
Distribution
The substance is essentially unlikely to be distributed and, if administered parenterally, is likely to remain at the site of administration.
Metabolism
Given the solubility profile of the material it is unlikely to become available for metabolism.
Excretion
Given the solubility profile of the substance, it is not likely to be available for excretion. If particles lodge in the alveolus following inhalation, they will be dealt with largely as insoluble particulates, and if the substance is administered orally it is likely to appear in faeces unabsorbed.
Conclusion
Given the solubility profile and particle size, the substance is unlikely to be absorbed orally or dermally, and is unlikely to be inhaled and retained. Given the solubility of the material, it is also unlikely to become available for metabolism or excretion. If particles lodge in the alveolus following inhalation, they will be dealt with largely as insoluble particulates, and if the substance is administered orally it is likely to appear in faeces unabsorbed.
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.
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