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Diss Factsheets
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EC number: 700-651-7 | CAS number: 692-49-9
- 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
Key value for chemical safety assessment
- Bioaccumulation potential:
- no bioaccumulation potential
Additional information
Male and female rats were exposed to the substance via inhalation and toxicokinetics parameters including absorption, distribution, metabolism, and excretion were evaluated. These parameters subsequently provided information on the potential for accumulation of the test substance in the tissues/organs that were evaluated. The results indicated that test substance is systemically absorbed via the inhalation route of exposure and no indication of accumulation potential was identified. The absorption of the test substance was rapid with steady-state in whole blood occurring by 2 hours during a 6-hour exposure. The pharmacokinetic behavior of the substance in blood was similar between males and females following various exposure concentrations and durations with whole blood elimination half-lives ranging from 0.19-1.5 hours. The test substance was distributed throughout the tissues within 30 minutes after a single 6-hour exposure to 10000 ppm of the substance and there was no indication of accumulation potential. Excretion was substantially complete by 18 hours post exposure. The pattern of distribution and excretion was similar across sex and dose. The relatively small amounts of parent test substance that was detected in the urine and faeces were likely due to volatility during collection. Elimination via exhalation could not be determined under the conditions of this study. Metabolism of the absorbed dose was extensive and was characterized by identified components in blood, tissues, bile, urine, and faeces. The primary biotransformation steps for the test substance appear to be either oxidation or direct conjugation with glutathione. Additional secondary metabolism resulted in phase I and phase II metabolites including oxidation to a ketone, formation of a second glutathione conjugate, or further hydrolysis to dihydroxyl-test substance and glucuronidation. The glutathione conjugates were degraded to cysteine conjugates and N-acetylated cysteine conjugates. The metabolic profile appears to be qualitatively similar between male and female rats.
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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