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EC number: 203-618-0 | CAS number: 108-80-5
- 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

Particle size distribution (Granulometry)
Administrative data
Link to relevant study record(s)
- Endpoint:
- particle size distribution (granulometry)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 110 (Particle Size Distribution / Fibre Length and Diameter Distributions)
- GLP compliance:
- yes
- Type of method:
- sieving
- Type of distribution:
- counted distribution
- No.:
- #1
- Size:
- < 100 µm
- Distribution:
- ca. 38 %
- No.:
- #2
- Size:
- < 10 µm
- Distribution:
- ca. 0.734 %
- No.:
- #3
- Size:
- < 5.5 µm
- Distribution:
- ca. 0.356 %
- Conclusions:
- Proportion of CYA having an inhalable particle size < 100 µm (sieve method) = 38.7%
Proportion of CYA having a thoracic particle size < 10.0µm (cascade impactor method) = 0.734%
Proportion of CYA having a respirable particle size < 5.5 µm (cascade impactor method) = 0.356%
Reference
Table 1: Results of sieving procedure
Sieve aperture size (µm) |
100 |
Mass of test material transferred to sieve (g) |
10.58 |
Mass of test material passed through sieve (g) |
4.09 |
Test material less than sieve aperture size (%) |
38.7 |
Table 2: Overall cumulative amounts of cyanuric acid with a particle size < 10 µm (%) from determinations 1 to 3:
Determination |
Cumulative amount of test material < 10.0 µm (%) |
Mean cumulative amount of test material < 10.0 µm (%) |
1 |
1.22 |
0.734 |
2 |
0.665 |
|
3 |
0.317 |
Table 3: Overall cumulative amounts of cyanuric acid with a particle size < 5.5 µm (%) from determinations 1 to 3
Determination |
Cumulative amount of test material < 5.5 µm (%) |
Mean cumulative amount of test material < 5.5 µm (%) |
1 |
0.461 |
0.356 |
2 |
0.439 |
|
3 |
0.169 |
Too few particles were of a size less than 10.0 µm to allow accurate assessment of mass median aerodynamic diameter. Representative sampling was ensured by rolling the sample container for approximately 10 minutes and sampling from the top, middle and bottom prior to definitive testing. The inhalable fraction is defined as the mass fraction of particles which can be inhaled by nose or mouth, the thoracic fraction is defined as the mass fraction of particles that passes the larnyx and the respirable fraction is defined as the mass fraction of particles that reaches the alveoli.
Description of key information
Particle size distribution was performed according to OECD guideline 110
Additional information
Proportion of CYA having an inhalable particle size < 100 µm (sieve method) = 38.7%
Proportion of CYA having a thoracic particle size < 10.0µm (cascade impactor method) = 0.734%
Proportion of CYA having a respirable particle size < 5.5 µm (cascade impactor method) = 0.356%
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