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EC number: 234-329-8 | CAS number: 11103-86-9
- 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
A valid test on acute inhalation toxicity of another sparingly water soluble chromate, strontium chromate, exists and is utilised for read-across. In acute oral toxicity, a poorly described study on strontium chromate is notified but the LD50 is based on read-across from a sparingly water soluble chromate. There is no non-human information on acute dermal toxicity of zinc potassium chromate. Human information on zinc potassium chromate is also lacking.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 327 mg/kg bw
Acute toxicity: via inhalation route
Endpoint conclusion
- Dose descriptor:
- LC50
- Value:
- 270 mg/m³ air
Acute toxicity: via dermal route
Endpoint conclusion
- Value:
- mg/kg bw
Additional information
According to REACH guidelines with>1,000 t/a substances, two toxicity tests are required (oral and inhalation or dermal acute toxicity tests) for showing acute toxicity of a substance. Based on the assumptions made in the toxicokinetics of the bioavailability, exposure via inhalation route is relevant for chromates. As zinc potassium chromate is a sparingly water soluble chromate, read-across from other sparingly water soluble chromates as strontium chromate is the priority when regarding the acute toxicity of zinc potassium chromate. In a well-performed acute inhalation toxicity test with strontium chromate, the LD50 was between 0.27 and 0.51 mg/L air, suggesting category 2 in classification. There are two other studies on acute toxicity of strontium chromate. In these, the substance was orally or intratracheally administered in rats, giving a LD50value of 3,118 mg/kg bw (795 mg Cr/kg) and 16.6 mg/kg (4.2 mg Cr/kg), respectively. According to this acute oral toxicity study and read-across approach from strontium chromate, there would not be classification for zinc potassium chromate. There is no non-human information on acute dermal toxicity of zinc potassium chromate. Human information on zinc potassium chromate is also lacking..
Data with highly water soluble chromates exist, but this data can be regarded as worst case scenario. This is because both the well-documented inhalation study (LC500.27-0.51 mg/L) and the supporting oral toxicity study (LD503,118 mg/kg bw) with strontium chromate give evidence on the lower acute toxicity also for zinc potassium chromate compared to the results received in studies with highly water soluble hexavalent chromium compounds (e.g. in Gad et al. 1986: LC50for acute inhalation toxicity 0.094-0.158 mg/L, and LD50for acute oral toxicity 51.1-57.2 mg/kg bw). For acute inhalation toxicity, classification of zinc potassium chromate into category 2 is justified. Furthermore, it is reasonable to judge acute oral toxicity of zinc potassium chromate to category 4 as a study with sparingly soluble calcium chromate suggest. This is milder classification than with highly water soluble chromates but tighter than in the poorly described study with strontium chromate.
Justification for classification or non-classification
Conclusion: Zinc potassium chromate is classified for acute oral toxicity as 'harmful if swallowed' (category 4), and for acute inhalation toxicity 'fatal if inhaled' (category 2). No further testing is suggested.
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