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EC number: 203-614-9 | CAS number: 108-77-0
- 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
Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1991-08-19 to 1991-09-23
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP guideline study Guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 992
- Report date:
- 1992
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 403 (Acute Inhalation Toxicity)
- Version / remarks:
- adopted: 1981-02-02
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Test type:
- standard acute method
Test material
- Reference substance name:
- 2,4,6-trichloro-1,3,5-triazine
- EC Number:
- 203-614-9
- EC Name:
- 2,4,6-trichloro-1,3,5-triazine
- Cas Number:
- 108-77-0
- Molecular formula:
- C3Cl3N3
- IUPAC Name:
- trichloro-1,3,5-triazine
- Reference substance name:
- cyanuric chloride
- IUPAC Name:
- cyanuric chloride
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
Constituent 1
Constituent 2
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Versuchstierzucht Winkelmann, Borchen, Kreis Paderborn, Germany
- Age at study initiation: 2 to 3 months
- Weight at study initiation: 170 - 210 g
- Housing: 5 animals per cage (Makrolon type III)
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 °C +- 2
- Humidity (%): ca. 50 %
- Air changes (per hr): ca. 10
- Photoperiod (hrs dark / hrs light): 12/12
Administration / exposure
- Route of administration:
- inhalation: aerosol
- Type of inhalation exposure:
- nose/head only
- Vehicle:
- other: unchanged (no vehicle)
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: inhalation chamber (TSE Labortechnik, Bad Homburg)
- Exposure chamber volume: 20 L
- Method of conditioning air: VIA-Drucklufttrockner
- System of generating particulates/aerosols: Wright-Dust-Feeder + self constructed metal cyclone as particle precipitator (used at higher doses)
- Method of particle size determination: Berner- or Andersen-cascade impactor
- Treatment of exhaust air: aerosol filter (absorbent cotton) and + combustor
- Temperature, humidity, pressure in air chamber: 24 °C, 25 %
TEST ATMOSPHERE
- Brief description of analytical method used: GC
- Samples taken from breathing zone: yes
TEST ATMOSPHERE (if not tabulated)
- Particle size distribution: see "any other information on materials and methods including tables"
- MMAD (Mass median aerodynamic diameter) / GSD (Geometric st. dev.): see "any other information on materials and methods including tables"
- stability of test atmosphere: total carbon analyzer (Ratfisch RS 55) - Analytical verification of test atmosphere concentrations:
- yes
- Remarks:
- see (I)
- Duration of exposure:
- 4 h
- Concentrations:
- - 37.6, 150.6, 177.3, 289.3, 449.1 mg/m³, (respective contribution to the concentrations by particles: 0.0, 2.3, 18.8, 44.7, 165.5 mg/m³)
- No. of animals per sex per dose:
- - 5
- Control animals:
- other: animals of the study were compared to periodically tested animals (once per 3 month, clean air)
- Details on study design:
- - Duration of observation period following administration: 28 days
- Frequency of observations: several times on day 0, daily thereafter; frequency of weighing: day 1, day 3, day 7, day 14 and day 28
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight,organ weights, gross necropsy - Statistics:
- Maximum-Likelihood where applicable
Results and discussion
Effect levelsopen allclose all
- Sex:
- male/female
- Dose descriptor:
- LC50
- Effect level:
- 170 mg/m³ air
- Based on:
- test mat.
- 95% CL:
- 137 - 213
- Exp. duration:
- 4 h
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- 150 mg/m³ air
- Based on:
- test mat.
- Exp. duration:
- 4 h
- Remarks on result:
- other: this value was approximated, as the slope of dose response curve was very steep
- Sex:
- female
- Dose descriptor:
- LC50
- Effect level:
- 201 mg/m³ air
- Based on:
- test mat.
- 95% CL:
- 157.7 - 257.9
- Exp. duration:
- 4 h
- Mortality:
- - see table on mortality, body weight decrease, clinical signs and necroscopy
- mortality occurred between day 1 and day 14 post application - Clinical signs:
- other: - clinical signs reported for days 0,1,2,3,7,14,21,28 - see table on mortality, body weight decrease, clinical signs and necroscopy
- Body weight:
- - see table on mortality, body weight decrease, clinical signs and necroscopy
- Gross pathology:
- - see table on mortality, body weight decrease, clinical signs and necroscopy
- Other findings:
- - reflexes: see table on mortality, body weight decrease, clinical signs and necroscopy
Applicant's summary and conclusion
- Interpretation of results:
- Category 2 based on GHS criteria
- Remarks:
- Migrated information
- Conclusions:
- Under the conditions of this acute inhalation toxicity study a combined LC50 for both sexes of 170 mg/m³ air (137 — 213, 95% CL) and a LD50 for males of 150 mg/m³ air were deduced for rats.
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