Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 446-630-3 | CAS number: 181587-01-9
- 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
Phototransformation in water
Administrative data
Link to relevant study record(s)
- Endpoint:
- phototransformation in water
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 23 Apr 1998 - 30 Dec 1999
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Study type:
- direct photolysis
- Qualifier:
- according to guideline
- Guideline:
- EPA Guideline Subdivision N 161-2 (Photodegradation Studies in Water)
- Qualifier:
- according to guideline
- Guideline:
- other: EU Directive 91/414/EEC, Annex IIA 2.9.2
- Qualifier:
- according to guideline
- Guideline:
- other: SETAC: Procedures for assessing the environmental fate and ecotoxicity of pesticides, 1995, 10. Aqueous photolysis
- GLP compliance:
- yes
- Radiolabelling:
- yes
- Analytical method:
- high-performance liquid chromatography
- Details on sampling:
- - Sampling intervals for the parent/transformation products: Sampling was carried out after 0, 3, 5, 8, 12.3 and 16 hours of irradiation. For the dark controls, the sampling time was 16 h.
- Sampling method: Sampled aliquots were split up: Radioactivity was counted in 2 x 200 µL, 2 x 1.5 mL were removed for HPLC analysis, 5 mL were removed for HPLC analysis
- Sampling intervals/times for pH measurements: pH was checked at each sampling time point.
- Sampling intervals/times for sterility check: Sterility was checked in aliquots from 16 h samples.
- Sample storage conditions before analysis: Instant analysis or storage at -20 °C; stability of the compounds under this condition was shown. - Buffers:
- - pH: 5
- Type and final molarity of buffer: 18.25 mM citric acid
- Composition of buffer: 8.4 g of citric acid was dissolved in 2 L deionised water and the pH was adjusted with 1M NaOH - Light source:
- Xenon lamp
- Light spectrum: wavelength in nm:
- > 290
- Details on light source:
- - Emission wavelength spectrum: > 290
- Filters used and their purpose: Special ultra-violet glass was used to remove radiation below 290 nm and give a spectral distribution approximating D65 radiation.
- Light intensity at sample and area irradiated: The intensity of the incident light measured was found to be 730 W/m2.
- Relative light intensity based on intensity of sunlight: 5.06 hours of Suntest irradiation under experimental conditions are equivalent to one day of summer sunlight at the latitudes 20°-50° North or 1 hour of Suntest irradiation = 0.198 days of summer sunlight. - Details on test conditions:
- TEST SYSTEM
- Type, material and volume of test apparatus/vessels: Pyrex photochemical reactors, 100 mL
- Sterilisation method: 35 min at 121 °C
- If no traps were used, type of test system: closed
- Test temperature: 24.8 - 25.2 °C
TEST MEDIUM
- Volume used/treatment: 100 mL
- Kind and purity of water: Deionised water, further purified by means of an Elgastat UHP apparatus, resistivity > 18 MΩ*cm
- Preparation of test medium: 99 mL of buffer pH 5 solution was poured into the photochemical reactors using a sterilised graduated measuring cylinder. 1.0 mL of a solution containing 14C-RPA107382 at a nominal concentration of 0.303 mg/mL in acetonitrile was added to each reactor using an automatic pipette fitted with a sterile tip. The final concentration of the test substance was 3.03 µg/mL.
- Identity and concentration of co-solvent: acetonitrile, 1% (v/v)
REPLICATION
- No. of replicates (dark): 2
- No. of replicates (irradiated): 2 - Duration:
- 16 h
- Temp.:
- 25 °C
- Initial conc. measured:
- 3.03 other: µg/mL (nominal)
- Reference substance:
- no
- Dark controls:
- yes
- Remarks:
- Two Schott bottles were placed at 25 ± 1 °C in the dark for 16 h.
- Computational methods:
- - Half-lives or DT50 values: Calculations were made with Excel v7.0 (Microsoft). r2 = 0.9952 for Ethiprole degradation kinetics which was found to be pseudo-first order.
- Parameter:
- max lambda
- Value:
- 203 nm
- Remarks:
- neutral medium
- Parameter:
- max lambda
- Value:
- 278.5 nm
- Remarks:
- neutral medium
- Parameter:
- max lambda
- Value:
- 329 nm
- Remarks:
- neutral medium
- % Degr.:
- 81.4
- Sampling time:
- 16 h
- DT50:
- 6.46 h
- Test condition:
- 16 hours continuous Xenon-lamp irradiation
- DT50:
- 1.3 d
- Test condition:
- Calculated for summer sunlight in Florida, USA
- Transformation products:
- yes
- No.:
- #1
- No.:
- #2
- No.:
- #3
- No.:
- #4
- Details on results:
- TEST CONDITIONS
- pH, sterility, temperature, and other experimental conditions maintained throughout the study: Yes
TRANSFORMATION PRODUCTS in the dark controls
- No degradation was observed.
TRANSFORMATION PRODUCTS in the irradiated test samples
- RPA 157925: 21.0% on day 3 and 18.5% at test end
- Met 10.3: 5.5% on day 3 and 37.2% at test end
- Met 9.3: 1.5% on day 3 and 9.2% at test end
- Met 6.5: 1.5% on day 5 and 7.5% at test end
VOLATILIZATION
- No volatiles were generated. - Validity criteria fulfilled:
- not applicable
Reference
Mass balance: For each individual sample, the total radioactivity balance ranged from 94.2 to 101.1% of the initial applied radioactivity (mean: 97.3% of applied).
Description of key information
DT50 = 1.3 d in summer sunlight (20 - 50 °North) (EPA Guideline Subdivision N, 161-2)
Key value for chemical safety assessment
- Half-life in water:
- 1.3 d
Additional information
One study investigating the Phototransformation of the substance in water is available following GLP and EPA Guideline Subdivision N, 161-2. A half-life of 6.46 hours was determined at continuous irradiation (Xenon lamp) corresponding to 1.3 days of summer sunlight in Florida (20 - 50 °North). Photodegradation can be considered as an important route of degradation in an aqueous environment.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.