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EC number: 231-211-8 | CAS number: 7447-40-7
- 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: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: only females used
Data source
Referenceopen allclose all
- Reference Type:
- publication
- Title:
- The acute oral toxicity of potassium chloride
- Author:
- Boyd EM, Shanas MN
- Year:
- 1 961
- Bibliographic source:
- Arch INt Pharmarodyn. 313, 275-283
- Reference Type:
- review article or handbook
- Title:
- Potassium chloride (CAS-Nr. 7447-40-7)
- Author:
- UNEP
- Year:
- 2 003
- Bibliographic source:
- United Nations Environmental Program
Materials and methods
- Principles of method if other than guideline:
- single oral application of different doses dissolved in water were given by gavage and animals were observed for clinical signs and mortality followed by autopsy upon non-survivors and of survivors 14 days after dosing
- GLP compliance:
- not specified
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Potassium chloride
- EC Number:
- 231-211-8
- EC Name:
- Potassium chloride
- Cas Number:
- 7447-40-7
- Molecular formula:
- KCl
- IUPAC Name:
- potassium chloride
- Details on test material:
- no details given
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 200-300 g
- Fasting period before study: 16 h
- Housing: indiviually in metabolism cages
- Diet ad libitum
- Water ad libitum
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- water
- Details on oral exposure:
- Each dose was dissolved in water an given in a volume of 20 ml/kg bw
- Doses:
- 0, 2100, 2400, 2700, 3300, 3600, 3900 mg/kg bw
- No. of animals per sex per dose:
- a total of 109 female mice were used (details not given)
- Control animals:
- yes
- Details on study design:
- single oral application of different doses dissolved in water were given by gavage and amimals were observed for clinical signs and mortality followed by autopsy upon non-survivors and of survivors 14 days after dosing. Each dose was dissolved in water an given in a volume of 20 ml/kg bw
- Statistics:
- t tests of significance of differences between means after the methods of Croxton
Results and discussion
Effect levels
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- ca. 3 020 mg/kg bw
- Remarks on result:
- other: death occurred in less than 2 hours after dosing due to respiratory failure and prostration was the most common pre-mortem clinical sign
- Mortality:
- Death occurred
in less than 2 hours in 62 % of the animals;
in 3-6 hours in 25 % of the animals and
in 7-12 h in 13 % of the animals - Clinical signs:
- other: the most common pre-mortem clinical sign was prostration, tonic clonic convulsion occurred in one third of the animals Death was due to respiratory failure Survivorshad anorexiam polydipsiy polyuriam fever convulsive movements and gastrointestinal dist
- Gross pathology:
- At autopsy, the parietal cells mucous neck cells and surface epithelium of the pyloric stomac were shrunken and there was loss of weight of this organ.
There were also areas of capillary and venous congestion in the lamina propria and submucosa in the pyloric stomach and occasional hemorrhage and necrosis of the surface epithelium. The heart was dilated with blood and the respiratory alveoli were frequently collapsed; the spleen was contracted. The columnar epithelium covering the intestinal villi was shrunken and the goblet cells dilated. There were area of early necrosis in the renal tubular epithelium.
Applicant's summary and conclusion
- Executive summary:
In an acute oral toxicity study female Wistar rats received 0, 2100, 2400, 2700, 3300, 3600, 3900 mg/kg bw potassium chloride dissolved in water. The LD50 value has been determined 3020 mg/kg bw. Clinical signs of intoxication in animals that died included convulsions followed by exhaustion and respiratory failure Autopsy revealed signs of irritant gastro-enterisis and necrosis appeared in the renal tubular epithelium. Animals that survived had convulsive movements diarrheam or sonstipation loss of appetite increase thirst and urine excretion and fever, Measurements of clinical sigh´ns were within the normal range within 2 -3 days and organ weights and water levels returned to normal limits in survivors at 2 weeks after administration of potassium chloride (Boyd 1969, UNEP 2003)
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