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Diss Factsheets
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EC number: 209-162-9 | CAS number: 557-21-1
- 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
- Study period:
- 2016
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 016
- Report date:
- 2016
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
- Deviations:
- not specified
- GLP compliance:
- yes
- Test type:
- acute toxic class method
Test material
- Reference substance name:
- Zinc cyanide
- EC Number:
- 209-162-9
- EC Name:
- Zinc cyanide
- Cas Number:
- 557-21-1
- Molecular formula:
- Zn(CN)2
- IUPAC Name:
- ZINC DICYANIDE
- Test material form:
- solid: particulate/powder
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- female
Administration / exposure
- Route of administration:
- other: gastric intubation
- Vehicle:
- other: Mineral oil
- Details on oral exposure:
- Animals were dosed via gastric intubation with disposable syringes fitted with intubation tubes. Animals were fasted overnight, approximately 12 hours prior to dosing. Drinking water was provided ad libitum. Feed was provided approximately 3 - 4 hours post dosing
- Doses:
- Four dose groups of three females per group were utilized as follows: Step 1, 2: 50 mg/kg bw, Step 3, 4: 300 mg/kg bw, Step 5: 2,000 mg/kg bw of the test substance
- No. of animals per sex per dose:
- 3
- Control animals:
- not specified
- Details on study design:
- Step 1, 2: 50 mg/kg bw, Step 3, 4: 300 mg/kg bw, Step 5: 2,000 mg/kg bw of the test substance. After the administration, the number of mortality were observed for more than 3 days. All animals were monitored for clinical signs and body weight changes during the 14-day observation
period after administration. They were subjected to gross necropsy at the end of the observation period. - Statistics:
- Statistical analysis was not performed.
Results and discussion
Effect levels
- Key result
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- > 300 mg/kg bw
- Based on:
- test mat.
- Mortality:
- There were deaths in all animals at step 5. There were no deaths in any animals at step 1 ~ 4.
- Clinical signs:
- other: There were no clinical signs of in step 1(50 mg/kg bw), step 3(300 mg/kg bw) throughout the course of the study. Soiled perineal region in one animal at each step 2 (50 mg/kg bw) were evident on Day 1 after dosing. Decrease in locomotor activity, irregula
- Gross pathology:
- No grossly visible findings were evident in the all steps.
Applicant's summary and conclusion
- Interpretation of results:
- Category 4 based on GHS criteria
- Conclusions:
- As a result of the acute oral toxicity study in Sprague-Dawley rats, no mortalities were observed at 50 mg/kg bw(in step 1 and 2) and 300 mg/kg bw(in step 3 and 4), 3 mortalities were observed at 2,000 mg/kg bw(in step 5). In consequences, GHS classification of the test substance, Zinc cyanide was classified to be ‘Category 4 (> 300 mg/kg bw ~ 2,000 mg/kg bw).
- Executive summary:
For that endpoint, one reliable study to assess the acute toxicity oral on the registered substance on rats was available. The study was performed according to the OECD 423 guideline.
Under the experimental conditions, the registered substance " Zinc cyanide batch n°10185145" has an LD50 above 300mg/L. Therfore, GHS classification of the test substance, Zinc cyanide was classified to be ‘Category 4 (> 300 mg/kg bw ~ 2,000 mg/kg bw).
The validity criteria were successful and the study was therefore regarded as acceptable for that endpoint.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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