Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 406-260-5 | CAS number: 58834-75-6 BTN; VPO CATALYST
- 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
Additional information
In vitro
Genetic toxicity was evaluated in a bacterial reverse mutation assay performed under GLP according to OECD guideline 471. Bacteria strains TA98, TA1535, TA1538, TA100 and TA1537 were treated with concentrations up to 2500 μg/plate with and without Aroclor 1254 induced rat S-9 liver enzyme mix. As result, vanadyl pyrophosphate was not mutagenic under the conditions of test.
Genetic toxicity in mammalian cells was analyzed in a mammalian chromosome aberration test which was performed under GLP according to OECD guideline 473. BTN/A treated human lymphocyte cultures treated with 40 μg/mL without metabolic activation and treated with a concentration of 200 μg/mL with metabolic activation by Aroclor 1254 induced rat S-9 liver enzyme mix showed several cases of chromatid separation. Although this effect was more pronounced at the higher concentration of vanadyl pyrophosphate used in the preliminary study, this effect is believed to indicate a non-specific effect on chromosome morphology. However, as this is not an indicator of clastogenic activity of the test material, no mutagenicity was found.
Due to the lack of an in vtro mutagenicity study, a published study with the structural analogue vanadium oxide sulphate was used for read-across (Galli et al., 1991). As result, no gene mutation in the HPRT locus of V79 cells was found when the cells were treated with concentrations of 1, 2, 5 and 7.5 mM with and without metabolic activation by mouse hepatic S-9 mix.
In vivo
The in vivo exposure of male and female CD-1 mice with oral doses of 500, 1000, 2000 mg/kg did not induce chromosome aberrations.
Short description of key information:
in vitro:
- gene mutataion in bacteria: negative
- gene mutation in mammalian cells: negative
- chromosome aberration in mammalian cells: negative
in vivo
- chromosome aberration (mouse): negative
Endpoint Conclusion:
Justification for classification or non-classification
The available data on genetic toxicity in vitro and in vivo are conclusive but not sufficient for classification.
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.