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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
Repeated dose toxicity: oral
Administrative data
- Endpoint:
- sub-chronic toxicity: oral
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Study period:
- 1982
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- This study did not utilize a guideline protocol or GLP, although this fact does not invalidate the information obtained. There was minimal information provided on the study substance, fewer animals per dose group were treated, and there is no information on whether test substance concentration was analyzed in the dietary feed. Experimental data was reviewed by the ECETOC Task Force, author of the JACC Report No. 53, “Cyanides of Hydrogen, Sodium and Potassium, and Acetone Cyanohydrin (CAS No. 74-90-8, 143-33-9, 151-50-8 and 75-86-5)”, 2007. The report is a weight of evidence approach to an extensive body of literature, much of which was undertaken prior to development of guidelines. The report was peer reviewed by the scientific non-governmental organization (NGO), which judged the data to be reliable with restrictions.
Data source
Reference
- Reference Type:
- publication
- Title:
- Cyanide, protein and iodine interactions in the performance and metabolism of rats
- Author:
- Tewe OO and Maner JH
- Year:
- 1 982
- Bibliographic source:
- J Environmental Pathol Toxicol Oncol 6:69-77.
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Subchronic feeding study (56) days of CD rats on various diets differing in protein content, iodide levels and cyanide levels.
- GLP compliance:
- not specified
- Limit test:
- no
Test material
- Reference substance name:
- Potassium cyanide
- EC Number:
- 205-792-3
- EC Name:
- Potassium cyanide
- Cas Number:
- 151-50-8
- IUPAC Name:
- potassium cyanide
- Details on test material:
- All cyanide salts ingested will be present, at the physiological pH of the stomach, as HCN.
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Weanling rats allocated on the basis of sex and body weight to 8 groups, each with 8 replicates.
Administration / exposure
- Route of administration:
- oral: feed
- Vehicle:
- unchanged (no vehicle)
- Analytical verification of doses or concentrations:
- not specified
- Duration of treatment / exposure:
- 56 days
- Frequency of treatment:
- daily
Doses / concentrations
- Remarks:
- Doses / Concentrations:
diets supplemented with 750 ppm KCN
Basis:
other: 40 mg/kg bw/day CN ion
- No. of animals per sex per dose:
- 4 per sex for 8 total
- Control animals:
- yes, plain diet
- Details on study design:
- Animals were individually housed in metabolism cages and urine collected and assayed for serum thiocyanate levels.
Examinations
- Sacrifice and pathology:
- Sacrificed by anesthesia with chloroform and blood obtained by cardiac puncture for determination of serum thiocyanate, proteins using a concentrimeter and protein bound iodine levels.
- Other examinations:
- The liver and kidney were removed, weighed, and frozen for rhodanese activity
- Statistics:
- Factorial analysis was carried out on the measured parameters by the method described by Steel and Torrie (1960).
Results and discussion
Results of examinations
- Clinical signs:
- no effects observed
- Mortality:
- no mortality observed
- Body weight and weight changes:
- effects observed, treatment-related
- Food consumption and compound intake (if feeding study):
- effects observed, treatment-related
- Food efficiency:
- no effects observed
- Haematological findings:
- no effects observed
- Clinical biochemistry findings:
- no effects observed
- Urinalysis findings:
- effects observed, treatment-related
- Organ weight findings including organ / body weight ratios:
- no effects observed
- Details on results:
- The presence of cyanide in the diets caused a non-significant reduction in both feed consumption and growth rate. Moverover, on protein deficient diets, the lowest body weight gain among the groups of rats was observed in the animals with cyanide (750 ppm) in the diet. Dietary cyanide significantly increased serum and urinary thiocyanate concentration. Interactions of protein deficiency and dietary cyanide also significantly reduced serum thiocyanate concentrations, while interactions of protein deficiency, cyanide and iodine deficiency reduced kidney protein content.
Effect levels
- Dose descriptor:
- NOAEL
- Effect level:
- > 40 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Remarks:
- nominal
- Sex:
- male/female
- Basis for effect level:
- other: as mg CN ion/kgbw/day
Target system / organ toxicity
- Critical effects observed:
- not specified
Any other information on results incl. tables
Table 3: Performance of Rats on Variables of Dietary Cyanide, protein and iodine | |||||||||
Parameters | Dietary Variables | ||||||||
Cyanide (ppm) | 0 | 0 | 750 | 750 | 0 | 0 | 750 | 750 | |
Potassium iodine (ppm) | 32 | 0 | 32 | 0 | 32 | 0 | 32 | 0 | |
Crude protein (%) | 15 | 15 | 15 | 15 | 8 | 8 | 8 | 8 | |
Daily feed intake, g | 15.6 ± 1.2 | 16.0 ± 1.0 | 15.3 ± 1.0 | 15.0 ± 0.8 | 8.3 ± 0.5 | 7.9 ± 0.4 | 6.2 ± 0.5 | 6.2 ± 0.5 | |
Daily weight gain, g | 4.3 ± 0.5 | 4.5 ± 0.6 | 4.1 ± 0.4 | 4.1 ± 0.4 | 0.63 ± 0.05 | 0.59 ± 0.06 | 0.41 ± 0.06 | 0.50 ± 0.05 | |
Feed efficiency | 3.6 ± 0.19 | 3.6 ± 0.23 | 3.7 ± 0.17 | 3.7 ± 0.22 | 13.2 ± 0.68 | 13.4 ± 1.49 | 15.1 ± 1.90 | 12.4 ± 0.91 | |
Protein efficiency ratio | 1.9 ± 0.09 | 2.0 ± 0.11 | 1.8 ± 0.08 | 1.8 ± 0.10 | 0.93 ± 0.01 | 0.92 ± 0.10 | 0.82 ± 0.19 | 1.00 ± 0.08 | |
Fresh weight of organs, as % body weight | |||||||||
Liver | 4.0 ± 0.1 | 3.9 ± 0.1 | 3.8 ± 0.08 | 3.9 ± 0.09 | 4.2 ± 0.2 | 4.0 ± 0.2 | 4.1 ± 0.1 | 4.1 ± 0.07 | |
Kidney | 0.60 ± 0.02 | 0.59 ± 0.01 | 0.59 ± 0.01 | 0.62 ± 0.03 | 0.87 ± 0.03 | 0.82 ± 0.08 | 0.93 ± 0.05 | 0.85 ± 0.02 | |
56 day growth study. Each value represents mean of 8 rats per treatment ± SEM |
Table 4: Metabolic Changes in Rats Fed Varying Levels of Dietary Cyanide, Protein and Iodine | |||||||||
Parameters | Dietary Variables | ||||||||
Cyanide (ppm) | 0 | 0 | 750 | 750 | 0 | 0 | 750 | 750 | |
Potassium iodine (ppm) | 32 | 0 | 32 | 0 | 32 | 0 | 32 | 0 | |
Crude protein (%) | 15 | 15 | 15 | 15 | 8 | 8 | 8 | 8 | |
Serum protein, g/100 ml | 6.5 ± 0.07 | 6.8 ± 0.08 | 6.4 ± 0.18 | 6.5 ± 0.18 | 4.4 ± 0.09 | 4.4 ± 0.04 | 4.5 ± 0.04 | 4.3 ± 0.20 | |
Serum protein bound iodine, microg/100 ml | 5.7 ± 0.28 | 3.7 ± 0.15 | 5.8 ± 0.20 | 3.7 ± 0.11 | 6.1 ± 0.29 | 3.9 ± 0.13 | 6.2 ± 0.25 | 3.9 ± 0.23 | |
Serum thiocyanate, mg/100 ml | 1.70 ± 0.05 | 1.69 ± 0.08 | 2.36 ± 0.10 | 2.73 ± 0.14 | 2.35 ± 0.04 | 2.37 ± 0.05 | 2.50 ± 0.19 | 2.59 ± 0.17 | |
Urinary thiocyanate, mg excreted/100 g feed intake | 2.13 ± 0.21 | 1.96 ± 0.05 | 5.66 ± 0.96 | 5.34 ± 0.53 | 0.75 ± 0.11 | 0.75 ± 0.34 | 2.86 ± 0.86 | 2.07 ± 0.79 | |
Rhodanese activity of tissues. mg thioc/min/g protein | |||||||||
Liver | 31.4 ± 2.5 | 31.1 ± 1.9 | 31.4 ± 1.5 | 30.2 ± 1.7 | 32.2 ± 1.8 | 31.1 ± 1.8 | 30.5 ± 1.5 | 31.8 ± 1.5 | |
Kidney | 26.2 ± 1.0 | 24.7 ± 0.9 | 24.3 ± 1.2 | 25.0 ± 0.8 | 23.0 ± 1.0 | 23.0 ± 1.0 | 24.4 ± 1.4 | 23.2 ± 1.0 | |
Protein content of tissues. mg/100 g fresh tissue weight | |||||||||
Liver | 25.8 ± 0.9 | 24.0 ± 1.1 | 23.6 ± 0.6 | 26.1 ± 1.1 | 23.6 ± 1.2 | 24.1 ± 1.2 | 23.0 ± 0.9 | 23.3 ± 0.8 | |
Kidney | 23.0 ± 1.2 | 21.9 ± 1.2 | 21.7 ± 1.0 | 21.7 ± 0.6 | 17.7 ± 0.9 | 19.2 ± 1.4 | 19.9 ± 1.2 | 19.0 ± 1.2 | |
Urinary thiocyanate values are those recorded during the first week of the study period. ± SEM |
Applicant's summary and conclusion
- Conclusions:
- Cyanide in a nutritionally adequate diet resulted in weight loss, which was exascerbated in a diet with inadequate protein. This level of 750 ppm cyanide did not cause cyanide intoxication. The NOAEL was greater than 40 mg CN ion/kg bw/d. Serum and urinary thiocyanate levels were increased. In a diet where protein and iodine content was deficient, kidney protein content and rhodanese was significantly reduced.
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