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EC number: 200-267-5 | CAS number: 56-34-8
- 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
Endpoint summary
Administrative data
Description of key information
Acute oral toxicity
LD50 was estimated to be 2630 mg/kg bw when rats were orally exposed with N, N, N-triethylethanaminium chloride (56-34-8)
Key value for chemical safety assessment
Acute toxicity: via oral route
Link to relevant study records
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Justification for type of information:
- Data is from peer-review journal
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- other: As mention below
- Principles of method if other than guideline:
- Acute oral toxicity study of N, N, N-triethylethanaminium chloride was performed in Rat
- GLP compliance:
- not specified
- Test type:
- fixed dose procedure
- Limit test:
- yes
- Specific details on test material used for the study:
- Name of test material (as cited in study report):Tetraethylammonium chloride
- Molecular formula :C8H20N.CI
- Molecular weight :165.706 g/mole
- Substance type:organic
- Physical state:Crystalline powder
-Purity:No data available
- Impurities (identity and concentrations):No data available - Species:
- rat
- Strain:
- other: Albino
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- No data available
- Route of administration:
- oral: unspecified
- Vehicle:
- water
- Details on oral exposure:
- Details on exposure
VEHICLE
- Concentration in vehicle: 40.6% test substance dissolved in distilled water
- Amount of vehicle (if gavage): No data available
- Justification for choice of vehicle: Readily dissolved in water
- Lot/batch no. (if required): No data available
- Purity: No data available
MAXIMUM DOSE VOLUME APPLIED: No data available
DOSAGE PREPARATION (if unusual): No data available
CLASS METHOD (if applicable)
- Rationale for the selection of the starting dose: No data available - Doses:
- 2630mg/kg
- No. of animals per sex per dose:
- 155
- Control animals:
- no
- Details on study design:
- No data available
- Statistics:
- No data available
- Preliminary study:
- No data available
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 2 630 mg/kg bw
- Based on:
- test mat.
- Remarks on result:
- other: Mortality observed
- Mortality:
- Mortality observed with 10-30 min due to respiratory failure
- Clinical signs:
- other: Tremors ,incoordination ,flaccid prostration
- Gross pathology:
- No data available
- Other findings:
- No data available
- Interpretation of results:
- other: Not classified
- Conclusions:
- LD50 was consiidered to be 2630mg/kg body weight .When albino rats were treated with N, N, N-triethylethanaminium chloride (56-34-8)
- Executive summary:
Acute oral toxicity study was done in albino rat using test material N, N, N-triethylethanaminium chloride (56-34-8).155 animals were used. 40.6% test substance dissolved in distilled water to get required dose concentration. Maximum tolerated dose i.e.95-100 % animal survived was determined to be 750.0mg/kg .Clinical signslikeTremors, incoordination, flaccid prostrationwere observed. Mortality observed with 10-30 min due to respiratory failure at dose 2630mg/kg/bw .Hence LD50 was determined2630mg/kg body weight. When albino rats were treated with N, N, N-triethylethanaminium chloride (56-34-8)
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 2 630 mg/kg bw
- Quality of whole database:
- Data is K2 obtain from peer- reviewed journal
Acute toxicity: via inhalation route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Acute toxicity: via dermal route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
In different studies N, N, N-triethylethanaminium chloride (56-34-8)has been investigated for acute oral toxicity to a greater or lesser extent. Often are the studies based on in vivo experiments and estimated data in rodents, i.e. most commonly in rats and mouse forN, N, N-triethylethanaminium chloride (56-34-8).
In experimental study for Tetraethylammonium chloride (CAS no 56-34-8) by Gruhzitet. al.(1948), acute oral toxicity was evaluated on albino rats by using Tetraethyl ammonium chloride in the concentration of 40.6 per cent commercial aqueous stock solution suitably diluted with distilled water. 95 to 100 per cent of animals survive at 750.0 mg/kg. The dose was considered to be maximum tolerated dose and 50 % mortality was observed at 2630.0 mg/kg in treated rats. Therefore, LD50 of Tetraethyl ammonium chloride was considered to be 2630.0 mg/kg in rats.
In a prediction done by SSS (2017) using the OECD QSAR toolbox with log kow as the primary descriptor, the acute oral toxicity was estimated forN,N,N-triethylethanaminium chloride (56-34-8),LD50 was estimated to be 2862mg/kg bw, when male and female Sprague-Dawley ratswereexposed withN,N,N-triethylethanaminium chloride (56-34-8)orally.
Also it is further supported by experimental study given by U.S. National Library of Medicine (ChemIDplus A TOXNET Database, 2017) on structurally for read across Tetrylammonium bromide (CAS no 71-91-0), acute oral toxicity was evaluated in mice by using Tetraethyl ammonium chloride at 2000 mg/kg. 50 % mortality was not observed at 2000 mg/kg. Therefore, LD50 of Tetrylammonium bromide (TEA) was considered to be >2000 mg/kg in mouse.
Also it is further supported by experimental study given by U.S. National Library of Medicine (ChemIDplus A TOXNET Database, 2017) on structurally similar read across substanceTetraethyl ammonium(66-40-0),mice were treated withTetraethyl ammonium(66-40-0))orally. No mortality was observed in treated rats at 2000 mg/kg bw. Therefore, LD50 was considered to be 2000mg/kg bw when rats were treated withTetraethyl ammonium(66-40-0), orally.
Thus, based on the above studies onN, N, N-triethylethanaminium chloride (56-34-8)and its read aross substancesTetrylammonium bromide (CAS no 71-91-0) andTetraethyl ammonium(66-40-0). It can be concluded that LD50 value is 2630.0mg/kg bw by oral route . Thus, comparing this value with the criteria of CLP regulationN, N, N-triethylethanaminium chloride (56-34-8)can be “not classified” of acute toxicity.
Justification for classification or non-classification
Thus, comparing this value with the criteria of CLP regulationN, N, N-triethylethanaminium chloride (56-34-8)can be “not classified” of acute toxicity.
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