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Diss Factsheets
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EC number: 200-821-6 | CAS number: 74-90-8
- 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
Key value for chemical safety assessment
Additional information
The mutagenicity of the chemicals of the cyanide family has been investigated in gene mutation assays in bacteria and mammalian cell lines using a variety of methods to induce metabolic activation. Cytotoxicity has been observed at the highest test concentrations. The studies of Hébert (1993), Monsanto (1983a) and Zeiger et al (1988) are considered to be the key studies for gene mutation in bacteria; for mammalian cells this is the HPRT test by Godek (1983). An in vitro Ames test with HCN in S. typhimurium strains TA1537, TA1538 and TA98 for detection of frame shift mutation and TA1535 and TA100 for base-pair substitutions was performed with and without metabolic activation. There was no indication of mutagenic activity of HCN under these conditions (Leuschner et al, 1983a cited by WHO, 1993). Chinese hamsters were orally dosed with HCN and preparations of metaphase cells were studied for structural chromosome aberrations. The incidence of aberrations or gaps was within the spontaneous range. Neither multiple aberrations nor pulverised metaphases were found. There was no indication of mutagenic properties relative to structural chromatid or chromosome damage in vivo (Leuschner et al, 1983b cited by WHO, 1993).
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
Mutagenicity studies performed similar to/according to OECD guidelines indicate that HCN and related cyanides are not mutagenic.
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