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EC number: 204-469-4 | CAS number: 121-44-8
- 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
Specific investigations: other studies
Administrative data
- Endpoint:
- specific investigations: other studies
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Acceptable, well-documented publication which meets basic scientifical principles.
Data source
Reference
- Reference Type:
- publication
- Title:
- Nasal Irritation and Pulmonary Toxicity of Aliphatic Amines in Mice.
- Author:
- Gagnaire, F., Azim S., Bonnet, P., Simon, P., Guenier, J.P., and J.de Ceaurriz
- Year:
- 1 989
- Bibliographic source:
- Journal of applied toxicology, Vol. 9(5), 301-304 (1989)
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Mice were exposed to TEA by inhalation to measure a decrease in respiratory rate as well as to determine pulmonary toxicity. The breathing frequency was used as an index of upper respiratory tract irritation.
- GLP compliance:
- no
- Type of method:
- in vivo
- Endpoint addressed:
- respiratory irritation
Test material
- Reference substance name:
- Triethylamine
- EC Number:
- 204-469-4
- EC Name:
- Triethylamine
- Cas Number:
- 121-44-8
- Molecular formula:
- C6H15N
- IUPAC Name:
- triethylamine
- Details on test material:
- - Name of test material (as cited in study report): Triethylamine
- Substance type:liquid or as a solution of the gaseous amine in water
- Analytical purity: high purity
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- Swiss
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source:IFFA CREDO, Domaine des Oncins, Saint Germain sur l'Arbresle
- Weight at study initiation: 20-25 g
- Diet (e.g. ad libitum): UAR-Alimentation, Villemoisson ad libitum
- Water (e.g. ad libitum): tab water ad libitum
- Acclimation period: 1 day
- Inhalationchamber: 200 l stainless-steel with adjustable airflow (10-30 m3/h), negative pressure to prevent leakage of test atmosphere
(additional airflow bubbled through the liquid amines and the vaporized compounds were diluted with air to the required concentration before entering the exposure chamber)
Administration / exposure
- Route of administration:
- other: inhalation: tracheal cannulation
- Vehicle:
- not specified
- Analytical verification of doses or concentrations:
- not specified
- Duration of treatment / exposure:
- 15 min
- Frequency of treatment:
- single exposure
- Post exposure period:
- 75 min (in pulmonary toxicity test)
Doses / concentrations
- Remarks:
- Doses / Concentrations:
4 to 6 different exposure concentrations, range 77 - 305 ppm
Basis:
nominal conc.
- No. of animals per sex per dose:
- 6
- Control animals:
- no
Results and discussion
- Details on results:
- RD 50 = 156 ppm, 95 % confidence interval (ppm), tentative standard on the basis of 0.1 RD 50 < 15
Any other information on results incl. tables
For all amines, except for allylamine and diallylamine, the onset of action was very rapid, ca. 30 s to 1 min. For both of the amines previously mentioned, the effect became maximal after 10-15 min of exposure. At the end of a 15-min exposure period, the recovery
of respiratory frequencies to the pre-exposure values was also rapid, ca. 1 min.
The effects were slower to develop than in non-cannulated mice, the maximal effects being obtained after 120 min of exposure. After the end of exposure there was incomplete, if any, recovery, especially for the highest concentrations.
Applicant's summary and conclusion
- Conclusions:
- TEA irritates the mucous membranes and the respiratory tract. In concentrations of 156 ppm a 50 % decrease of the respiratory rate in rats was found.
- Executive summary:
Previous studies with several chemicals have shown that the RD ,,values can be used successfully to predict safe industrial exposure". At 0.1 RDsO, humans would experience some slight discomfort and this should be the highest level permitted in industry. At 0.01 RD50bno sensory irritation is observed and a convenient threshold limit value (TLV) would be 0.3 RD50 the midpoint on a logarithmic scale between the. 0.1 and 0.01 RD50. The present data show that, for seven amines out of ten compounds for which TLVs exist (Table 2), the current TLVs are always < 0.1 RD50 but higher than 0.01 RD,,,. For dimethylamine, trimethylamine
and cyclohexylamine, a TLV of 10 pprn seems too high and should be divided by a factor of two.
The differences between RDSo and RDSoTC indicate that amines are essentially irritants for upper airways. While the respiratory rate responses of oronasally exposed mice indicative of nasal irritation set in rapidly and were reversible when exposure to the irritants
ceased, the respiratory rate responses of cannulated mice were slower to develop than in oronasally exposed mice, and no, or incomplete, recovery was observed after the end of exposure, when mice were allowed to breathe fresh air.
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