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EC number: 266-257-8 | CAS number: 66215-27-8
- 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
Toxicity to birds
Administrative data
- Endpoint:
- short-term toxicity to birds
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 1978/08/11 to 1978/08/19
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 978
- Report date:
- 1978
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 205 (Avian Dietary Toxicity Test)
- Deviations:
- yes
- Remarks:
- No analytical verification of test item in diet
- GLP compliance:
- no
Test material
- Reference substance name:
- N-cyclopropyl-1,3,5-triazine-2,4,6-triamine
- EC Number:
- 266-257-8
- EC Name:
- N-cyclopropyl-1,3,5-triazine-2,4,6-triamine
- Cas Number:
- 66215-27-8
- Molecular formula:
- C6H10N6
- IUPAC Name:
- N2-cyclopropyl-1,3,5-triazine-2,4,6-triamine
Constituent 1
- Dose method:
- homogenously mixed into feed (accounts for technical substances)
- Analytical monitoring:
- no
- Vehicle:
- yes
- Remarks:
- olive oil
- Details on preparation and analysis of diet:
- Homogeneous substance feed mixtures were prepared by blending a 1 and 10 % dilution of cyromazine or Dieldrin in olive oil (oleum olivae PH H VI) into pulverized commercial food.
Test organisms
- Test organisms (species):
- other: Peking duck (anas domestica)
- Details on test organisms:
- Experiments were performed on Peking ducks (Anas domestica) bred and raised on the premises, with an age of 5 to 10 days.
Study design
- Limit test:
- no
- Total exposure duration (if not single dose):
- 8 d
- Post exposure observation period:
- 3 days
- No. of animals per sex per dose and/or stage:
- Ten birds in 5 groups were established for each treatment and control
- Control animals:
- yes, concurrent no treatment
- Nominal and measured doses / concentrations:
- Nominal: 100, 600, 1000, 6000 and 10,000 mg/kg diet for cyromazine
- Details on test conditions:
- The birds were housed in a wure battery 10 to a cage. They were kept at a room temperature of 22 ± 1°C and a relative humidity of 55 ± 5 % and had free access to feed and water.
Examinations
- Details on examinations and observations:
- Throughout the 8-day treatment and observation period the birds were observed daily for rate of deaths, changes in general conditions and food consumption. Food consumption though measured accurately, was presented as approximate consumption only due to the unavoidable wastage by the birds. Bodyweights were recorded at initiation, after 5 days and at the end of the study.
- Reference substance (positive control):
- yes
- Remarks:
- positive control groups treated with 5 different dieldrin concentrations: 60, 100, 200, 300 and 600 mg/kg diet (nominal)
Results and discussion
Effect levelsopen allclose all
- Key result
- Duration (if not single dose):
- 8 d
- Dose descriptor:
- LC50
- Effect level:
- > 10 000 mg/kg diet
- Conc. / dose based on:
- act. ingr.
- Basis for effect:
- mortality
- Remarks on result:
- other: both male and female
- Duration (if not single dose):
- 8 d
- Dose descriptor:
- LC50
- Remarks:
- for positive control
- Effect level:
- 272 other: ppm
- Conc. / dose based on:
- other: positive control
- Basis for effect:
- mortality
- Mortality and sub-lethal effects:
- No mortalities were observed in any of the cyromazine treatments. However at the 6000 and 10,000 mg/kg diet treatments slight signs of ataxy, curved position and lethargy were noted within 2-3 days of test start although the birds had recovered by the end of the 3-day observation phase.
In concentrations with positive control, where mortalities occurred dyspnoea, jerkiness in gait, ataxy terminal wing beat convulsions and curved or ventral position were seen starting with the 2nd experimental day. These symptoms became more accentuated as the concentration was increased. - Results with reference substance (positive control):
- In the positive control item, during the 5-day treatment period, there was a concentration related decrease in food consumption in groups of 200 up to 600 ppm. It was again comparable to that of the controls at the end of the 3 observation days. The bodyweight gain of the birds in concentrations of 200 up to 600 ppm was retarded during the test and observation period.
- Further details on results:
- Effects of food consumption:
In cyromazine concentrations from 1000 up to 10000 ppm food consumption was decreased during the 5 treatment days. There was a clear tendency of recovery at the end of the 3 observation days.
For bodyweight, bodyweights were decreased during the 5 treatment days in concentrations of 6000 and 10000 ppm. There was a clear tendency to regress during the 3 observation days. - Reported statistics and error estimates:
- For birds treated with the test item an exact determination of LC50 was not possible, as in the higher concentrations the birds partially refused food during the 5 day treatment period; also no mortalities were observed at any treatment. For the positive control (dieldrin) treatment, the LC50 including 95% confidence limits were calculated by the logit model.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- not applicable
- Conclusions:
- The 8-day, short term dietary LC50 of cyromazine in the Peking duck (Anas domestica) is > 10000 mg/kg diet (the highest concentration tested), when fed to "5—day old Peking ducks (Anas domestica)" of both sexes. In the higher concentrations the birds partially refused food during the 5 day treatment period, therefore an exact LC50 determination was not possible.
The 8-day LC50 for positive control (Dieldrin) is 272 (182—433) ppm when fed under the same experimental conditions. - Executive summary:
The object of the present study was to provide information on the toxic hazard of this compound to wild birds. The 8-day- toxicity of the compound was investigated in the Peking duck (Anas domestica). The procedure adopted was based on the recommendations of the United States Department of the Interior Fish and Wildlife Service, reported in "Procedure for Evaluation of Acute Toxicity of Pesticides to Fish and Wildlife" of December 14, 1964. This study did not follow any guidelines, and therefore no validity criteria could be assessed.
Five groups of birds received feed with five different concentrations of the test compound for a 5-day period, the concentrations were 100, 600, 1000, 6000 and 10,000 mg/kg diet for cyromazine, and 60, 100, 200, 300 and 600 mg/kg for positive control item (dieldrin).
The short term dietary LC50 of cyromazine in the Peking duck (Anas domestica) is > 10000 mg/kg diet (the highest concentration tested), when fed to 5-day old Peking ducks (Anas domestica) of both sexes as no mortlaity was observed at any treatment. However, in the higher concentrations the birds partially refused food during the 5 day treatment period. The 8-day LC50 for Dieldrin is 272 (182—433) ppm when fed under the same experimental conditions
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