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EC number: 431-840-1 | CAS number: 87010-29-5 OXIPROPAZON; OXYPROPAZON
- 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
Additional information
3-(3-Hydroxy-propyl)-oxazolidin-2-on is a liquid which is miscible with water. lt has a very low volatility and a log Pow of -1.22.
Evidence for systemic availability of 3-(3-Hydroxy-propyl)-oxazolidin-2-on comes from the subacute toxicity study in rats (BASF AG, 2004). In this study with dietary concentrations of 0, 750, 3000, and 12000 mg/kg feed (corresponding to 0 and about 70, 290 and 1160 mg/kg bw/day), clinico-chemical effects (decreased serum urea in males and females; increased red blood cells and hematocrit in females) were observed at 12000 mg/kg feed. These effects are clear indicators of systemic availability of 3-(3-Hydroxypropyl)-oxazolidin-2on. Since these changes were reversible within a 2-week recovery period, excretion of 3-(3-Hydroxy-propyl)-oxazolidin-2-on and its metabolites appears to be rather rapid.
Considering the chemical structure of 3-(3-Hydroxy-propyl)-oxazolidin-2-on, metabolism may consist of:
-cleavage of the oxazolidinon ring at the ester moiety;
- oxidation of the 3-hydroxy group to the acid via intermediate formation of an aldehyde;
-conjugation of the 3-hydroxy-group.
All potential metabolites of the metabolic pathway described above are more polar and more water soluble than the parent and are expected to be excreted predominantly via the urine.
Studies on genotoxicity (Ames-Test, in vitro cytogenetics) were negative, i.e. there is no indication of a reactivity of 3-(3-Hydroxy-propyl)-oxazolidin-2-on or its metabolites under the test conditions.
Taking into account the low log Pow as well as the results of the 28-day study in rats and the considerations on metabolism, accumulation of 3-(3-Hydroxy-propyl)-oxazolidin-2-on is considered to be unlikely.
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