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EC number: 932-389-6 | CAS number: -
- 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 birds
Administrative data
- Endpoint:
- long-term toxicity to birds: reproduction test
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- January 1981-August 1981
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- The study was conducted under GLP and under the proposed guidelines of the United States Environmental Protection Agency (E.P.A.) § 163:71-4 Avian Reproduction and published in the Federal Register 10 July 1978, Part II, pages 29729- 29731. The study is well documented and it can be considered reliable without restrictions.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 982
- Report date:
- 1982
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- EPA OPP 71-4 (Avian Reproduction Test)
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- Reaction mass of (R)-cyano(3-phenoxyphenyl)methyl rel-(1R,3R)-3-((1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl)-2,2-dimethylcyclopropanecarboxylate and (R)-cyano(3-phenoxyphenyl)methyl rel-(1S,3S)-3-((1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl)-2,2-dimethylcyclopropanecarboxylate
- EC Number:
- 932-389-6
- Molecular formula:
- C23H19ClF3NO3
- IUPAC Name:
- Reaction mass of (R)-cyano(3-phenoxyphenyl)methyl rel-(1R,3R)-3-((1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl)-2,2-dimethylcyclopropanecarboxylate and (R)-cyano(3-phenoxyphenyl)methyl rel-(1S,3S)-3-((1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl)-2,2-dimethylcyclopropanecarboxylate
Constituent 1
Results and discussion
Applicant's summary and conclusion
- Conclusions:
- The study is considered to be reliable without restrictions.
- Executive summary:
The study was designed to determine the effect of dietary administration of cyhalothrin on reproduction in the Mallard duck.
The protocol was based on the proposed guidelines of the United States Environmental Protection Agency (E.P.A.) § 163:71-4 Avian Reproduction and published in the Federal Register 10 July 1978, Part II, pages 29729- 29731.
Under the conditions of this study there was no evidence that dietary administration of cyhalothrin at dose levels of 5 ppm and 50 ppm had any adverse effects on reproduction in the Mallard duck.
The results are summarized below.
Adults:
Mean analysed concentrations of cyhalothrin in avian diet were within 10% of nominal values. Concentrations of cyhalothrin in blended diet prepared to check homogeneity indicated a satisfactory mix of test compound in the diet. The stability of cyhalothrin in diet at ambient temperature in the animal room was confirmed during storage for 18 days.
The mortalities which occurred could not be considered to be related to treatment with cyhalothrin and were in most cases the result of fighting between the male birds in a pen. Bird health was generally good, the majority of observations made being related to the effects of fighting between the birds in a pen. This is unavoidable with group housing of Mallard ducks.
Group mean bodyweights and bodyweight changes were within normal limits and no treatment-related, statistically significant differences were found.
Food consumption was within normal limits and no statistically significant differences between treatments were found.
Evidence of bullying was noted in a large number of sporadic mortalities. These and other abnormalities which were observed in the sporadic mortalities were not considered to be related to treatment with cyhalothrin.
Eggs:
Over weeks 1 to 6 and 7 to 12 birds given cyhalothrin at50ppm produced significantly fewer eggs than the controlP<O.05).This is, however, probably not biologically significant since the total number of eggs laid for Group C (Cyhalothrin50ppm) was high (1419) in comparison with the control data (ranging between 877 and 1027 eggs per group) obtained at the Huntingdon Research Centre in 1980. Broken and cracked eggs were within normal limits and no treatment-related differences were found.
There were no significant differences in mean egg weights between the groups. The egg mass (total weight of eggs laid) was significantly lower for Group C (Cyhalothrin50ppm) than for the control(P<O.OS).However, since this is dependent on the number of eggs laid it is unlikely to be biologically significant.
Egg shell thickness was within normal limits and there were no treatment-related differences.
Incubation and candling:
Group B (Cyhalothrin 5 ppm) had a significantly lower proportion of infertile eggs than the control. The proportions for all groups were within normal limits.
No statistically significant differences between treatments were found and the proportions of early embryonic mortalities were within normal limits. About Late embryonic mortalities, the proportions were within normal limits and there were no treatment-related differences.
The proportions of ducklings which hatched were not significantly different between treatments and were within normal limits.
Ducklings:
No treatment-related abnormalities were noted about bird health. The mortalities which occurred were not considered to be
treatment-related. The percentages of birds surviving to 14 days were within normal limits and no statistically significant differences were found. Bodyweights at hatching and at 14 days were within normal limits and no statistically significant differences between treatments were found.
As per gross macroscopic post mortem examination no treatment-related abnormalities were found.
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