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EC number: 304-802-4 | CAS number: 94279-56-8
- 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
Acute Toxicity: dermal
Administrative data
- Endpoint:
- acute toxicity: dermal
- Type of information:
- other: Expert assessment
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Expert assessment as opposed to experimental result
Data source
Reference
- Reference Type:
- other: Expert Assessment
- Title:
- Unnamed
- Year:
- 2 015
- Report date:
- 2015
Materials and methods
- Principles of method if other than guideline:
- Assessment
- GLP compliance:
- no
- Test type:
- other: Assessment
Test material
- Reference substance name:
- Silicic acid (H4SiO4), zirconium(4+) salt (1:1), reaction products with sodium hydroxide
- EC Number:
- 304-802-4
- EC Name:
- Silicic acid (H4SiO4), zirconium(4+) salt (1:1), reaction products with sodium hydroxide
- Cas Number:
- 94279-56-8
- Molecular formula:
- Silicic acid (H4SiO4), zirconium(4+) salt (1:1), reaction products with sodium hydroxide
- IUPAC Name:
- Silicic acid (H4SiO4), zirconium(4+) salt (1:1), reaction products with sodium hydroxide
Constituent 1
Results and discussion
Effect levels
- Remarks on result:
- other: The substance in water has a pH of >13. Consequently, it could not be tested as is; it would he theoretically possible to test the material after neutralisation, however, the test substance in this scenario would cease to be the original substance.
Any other information on results incl. tables
Assessment
Applicant's summary and conclusion
- Interpretation of results:
- other: Assessment
- Executive summary:
This substance is the product of a reaction between Zircon (EC no 239-019-6) and sodium hydroxide. The substance in water has a pH of >13. Consequently, it could not be tested as is; it would he theoretically possible to test the material after neutralisation, however, the test substance in this scenario would cease to be the original substance. It would thus be more appropriate to assess the toxicity based on the toxicity of the sodium silicate part of the molecule and assess the systemic toxicity by reading across from other water-soluble zirconium salts. Zirconium acetate has been shown to have a dermal toxicity of >5000 mg/kg; in addition, toxicity of Silicic acid (H4SiO4), zirconium(4+) salt (1:1), reaction products with sodium hydroxide by the oral route has been assessed. An LD50 of approximately 1300 mg/kg has been established. This further supports the assertion of low systemic toxicity. In addition, a dermal toxicity study has been conducted for silicic acid, potassium salt (215-199-1), which showed an LD50 of >5000 mg/kg. Running an acute dermal study would add nothing to the hazard assessment for this substance, and risk management measures are driven primarily by its corrosive nature due to the high pH. Determination of acute toxicity by the dermal route is therefore considered unnecessary.
The above should be considered as an expert statement to waive the requirement for testing for acute toxicity by the dermal route under REACH Annex VIII for endpoint 8.5.3.
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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