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EC number: 231-561-1 | CAS number: 7632-51-1
- 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

Endpoint summary
Administrative data
Key value for chemical safety assessment
Genetic toxicity in vitro
Description of key information
- And In vitro tests on the mutagenic potential of VCl4 in bacteria are considered dispensable for principal considerations, since inorganic metal compounds are frequently negative in this assay due to limited capacity for uptake of metal ions (guidance on Information Requirements and Chemical Safety Assessment - Chapter R.7a: Endpoint Specific Guidance), an Ames study is not relevant for metal (guide 7a, p565).
- VCl4, in contact of humidity, gives VO2 and HCl. The modification of the pH, due the hydrochloric acid, are known to lead to artefactual, positive results which do not reflect intrinsic mutagenicity of the test substance. Therefore, positive results from these references should be considered with extreme care and require a very thorough case-by-case validation.
In accordance with REACH Annex XI, section 2, testing is technically not feasible as a consequence of the properties of the substance:
And there are sufficient data on the breakdown products (vanadium dioxide n°CAS: 12036-21-4) and hydrogen chloride n°CAS: 9004-54-0 were already registered in the frame of REACH) and the breakdown substance are exempted to Registration following Annex V (Entry I).
Link to relevant study records
- Endpoint:
- in vitro gene mutation study in bacteria
- Data waiving:
- study technically not feasible
- Justification for data waiving:
- other:
- Justification for type of information:
- JUSTIFICATION FOR DATA WAIVING
More the datawaiving based on section 2 of annex XI, the guidance 7a (guidance on Information Requirements and Chemical Safety Assessment - Chapter R.7a: Endpoint Specific Guidance) indictes that an Ames study is not relevant for metal (guide 7a, p565) - Endpoint:
- in vitro gene mutation study in mammalian cells
- Data waiving:
- study technically not feasible
- Justification for data waiving:
- other:
- Justification for type of information:
- JUSTIFICATION FOR DATA WAIVING
Annex XI - section 2. Testing is technically not feasible as a consequence of the properties of the substance (hydrolytically unstable substance and quasi-instantaneously degraded in contact with moist skin/ mucuous membranes to form VOCl2 and HCl. - Endpoint:
- in vitro cytogenicity / chromosome aberration study in mammalian cells
- Data waiving:
- study technically not feasible
- Justification for data waiving:
- other:
- Justification for type of information:
- JUSTIFICATION FOR DATA WAIVING
Annex XI - section 2. Testing is technically not feasible as a consequence of the properties of the substance (hydrolytically unstable substance and quasi-instantaneously degraded in contact with moist skin/ mucuous membranes to form VOCl2 and HCl.
Referenceopen allclose all
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Additional information
Justification for classification or non-classification
Vanadium tetrachloride quasi-instantaneously degraded in contact with moist skin or mucuous membranes to form Vanadium dioxide and hydrogen chloride. Testing Vanadium tetrachloride for genetic toxicity is for this reason not relevant at all, but breakdown products have to be considered (classification for Vanadium dioxide and hydrogen chloride have been elaborated in the frame of REACH).
For these reasons, no classification could be set for genetic toxicity.
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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