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EC number: 204-589-7 | CAS number: 122-99-6
- 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
Toxicity to other aquatic organisms
Administrative data
Link to relevant study record(s)
Description of key information
Additional information
Ovaries of adultX.laeviswere excised (stage V and VI) and exposed to different test concentrations of 2-phenoxyethanol in glass plates at 4°C for 24 hours in presence and absence of either progesterone or androstenedione. Germinal vesicle breakdown, as a marker of the final stage of amphibian oocyte maturation (oogenesis), was determined visually and was verified by cracking the fixed oocytes. Two independent triplicate measurements were conducted. The potency was expressed as IC25 at which 25% of progesterone or androstenedione-induced GVBD occurred and was determined to be 1.9 and 5.3 µg/L for 2-phenoxyethanol, respectively.
Further, the binding capacity of 2-phenoxyethanol to oocyte plasma membrane receptor and to androgen was investigated by adding [3H]progesterone and [3H]androstenedione to the exposed oocytes. Oocytes or oocyte plasma membrane proteins were exposed (microinjected) with 2-phenoxyethanol equivalent to the IC25 and added radiolabeled hormones were separated from the oocytes or plasma by filtration or centrifugation. The OMPR and AR binding capacity of 2-phenoxyethanol was determined to be 10.8% relative to progesterone and 25.1% relative to androstenedione, respectively.
It was not investigated whether the effect concentrations are cytotoxic to the oocytes and 2-phenoxyethanol acted via both pathways (oocyte plasma membrane receptorand and androgen). This bimodal inhibition was unexpected and raised questions about the specificity of the assay with regard to the biological relevance.
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