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Diss Factsheets
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EC number: 237-324-9 | CAS number: 13746-89-9
- 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
Repeated dose toxicity: inhalation
Administrative data
- Endpoint:
- sub-chronic toxicity: inhalation
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- other: Non guideline and non GLP study. Only one single intratracheal application of the test substance and observation of the test animals over 8 months.
Data source
Reference
- Reference Type:
- publication
- Title:
- Effect on the organism of rare, dispersed, and other metals, and their compounds used in industry: zirconium
- Author:
- Mogilevskaya, O. Ya
- Year:
- 1 968
- Bibliographic source:
- National Science Foundation: Toxicology of rare metals, Washington D.C., 1967, pg 44
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- GLP compliance:
- no
- Limit test:
- yes
Test material
- Reference substance name:
- Zirconium
- EC Number:
- 231-176-9
- EC Name:
- Zirconium
- Cas Number:
- 7440-67-7
- IUPAC Name:
- zirconium(2+)
Constituent 1
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- not specified
Administration / exposure
- Route of administration:
- inhalation
- Type of inhalation exposure:
- other: intratracheal
- Vehicle:
- other: physiological saline
- Remarks on MMAD:
- MMAD / GSD: 90 % of particles are smaller than 2 µm.
- Analytical verification of doses or concentrations:
- not specified
- Duration of treatment / exposure:
- 8 months
- Frequency of treatment:
- once at the beginning of the study.
Doses / concentrations
- Remarks:
- Doses / Concentrations:
50 mg suspended in physiological saline
Basis:
nominal conc.
- No. of animals per sex per dose:
- 26 animals
- Control animals:
- yes, concurrent no treatment
- Positive control:
- Not examined.
Examinations
- Observations and examinations performed and frequency:
- No data.
- Sacrifice and pathology:
- GROSS PATHOLOGY: Yes. Animals were killed after 4 and 8 months.
HISTOPATHOLOGY: Yes
Results and discussion
Results of examinations
- Clinical signs:
- no effects observed
- Mortality:
- no mortality observed
- Body weight and weight changes:
- no effects observed
- Food consumption and compound intake (if feeding study):
- not examined
- Food efficiency:
- not examined
- Water consumption and compound intake (if drinking water study):
- not examined
- Ophthalmological findings:
- not examined
- Haematological findings:
- not examined
- Clinical biochemistry findings:
- not examined
- Urinalysis findings:
- not examined
- Behaviour (functional findings):
- not examined
- Organ weight findings including organ / body weight ratios:
- not examined
- Gross pathological findings:
- no effects observed
- Histopathological findings: non-neoplastic:
- effects observed, treatment-related
- Description (incidence and severity):
- in the lungs
- Histopathological findings: neoplastic:
- not examined
- Details on results:
- CLINICAL SIGNS AND MORTALITY
No mortality was observed during the eight months observation period. All animals remained healthy.
BODY WEIGHT AND WEIGHT GAIN
The body weight differed only little from that of the control animals.
GROSS PATHOLOGY
No treatment related gross changes were observed in the organs of all animals.
HISTOPATHOLOGY: NON-NEOPLASTIC
The lungs of each animal (Pathology after 4 months) were examined microscopically and cellular accumulations around the dust particles were observed. Furthermore the thickening of the interalveolar septa was seen due to the proliferation of histiocytes and fibroblasts. Throughout the entire lung large amounts of dust were observed.
After eight months the process of cellular accumulation had progressed slowly with increasing number of connecting tissue fibers in the foci and in the thickening of the interalveolar septa. Proliferation of connective tissue cells and fibrosis around vessels and bronchi of all kinds was also observed. Furthermore areas of emphysema, and thickening and swelling of the blood vessels was seen. In the bronchial glands large amounts of dust were found.
Effect levels
- Dose descriptor:
- NOAEC
- Remarks on result:
- not determinable
- Remarks:
- no NOAEC identified
Target system / organ toxicity
- Critical effects observed:
- not specified
Applicant's summary and conclusion
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.