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Diss Factsheets
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EC number: 819-558-9 | CAS number: 2020359-04-8
- 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
Endpoint summary
Administrative data
Link to relevant study record(s)
Description of key information
ACD/ADME predicted data indicated that:(1)the compound could be absorbed in small intestinewith a low absorption rate,(2)it may pass the BBB easily,(3)it may have a moderate oral bioavailability between 30% and 70%,(4)it could bind with plasma proteins with a high binding ratio of 98%,(5)it might be an inhibitor of P-gp, and(6)it would not be an inhibitor of CYP450 and could be metabolized into hydroxyl metabolites. The DS/ADMET calculated data suggested:(1)the compound could pass the BBB;(2)it could be absorbed in small intestine;(3)it would not be an inhibitor of CYP450 2D6;(4)its binding ratio on plasma protein would be more than 95%.
In combination of predicted data from both softwares and corresponding literature reported pharmacokinetics of the compound Fluorene, it was predicted that1-(9,9-dibutyl-9H-fluoren-2-yl)-2-methyl-2-morpholinopropan-1-one could be absorbed in small intestinewith a low absorption rate, and its oral bioavailability would be at a middle level between 30% and 70%. It may pass the BBB easily to have contribution in brain. Its binding ratio on plasma proteins would be at a high level more than 95% but less than 99%. It might be an inhibitor of P-gp. The compound would not be an inhibitor of CYP450 and could be metabolized by corresponding enzymes. Since the compound contains the condensed ring of fluorene, it could be transferred to phenolic metabolites by phase I metabolism and even to glucoside metabolites by further phase II metabolismin vivo. These metabolites would have increased water solubility favorable for their excretion via the urine. Furthermore, 1-(9,9-dibutyl-9H-fluoren-2-yl)-2-methyl-2-morpholino-propan-1-one might also be excreted directly via the urine or feces, since the compound may have a very low absorption rate in intestine.Key value for chemical safety assessment
Additional information
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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