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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
Toxicity to reproduction
Administrative data
- Endpoint:
- fertility, other
- Remarks:
- based on test type (migrated information)
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Acceptable, well documented publication/study report which meets basic scientific principles
Data source
Reference
- Reference Type:
- publication
- Title:
- Reproductive Toxicity of Vanadyl Sulphate in Male Rats
- Author:
- Jain, G.C. et al.
- Year:
- 2 007
- Bibliographic source:
- Journal of Health Sciences, 53(1), 137-141
Materials and methods
- Principles of method if other than guideline:
- A group of seven male rats were dosed with 100 mg/kg bw/d via drinking water. During the five last days of the treatment period, they were cohabited with pro-estrus females. The males were sacrificed on day 61 and the testes and accessory organs were examined. Successfully mated females were allowed to litter.
- GLP compliance:
- no
- Limit test:
- yes
Test material
- Reference substance name:
- Vanadium oxide sulphate
- EC Number:
- 248-652-7
- EC Name:
- Vanadium oxide sulphate
- Cas Number:
- 27774-13-6
- IUPAC Name:
- oxovanadium(2+) sulfate
- Reference substance name:
- vanadyl sulphate
- IUPAC Name:
- vanadyl sulphate
- Details on test material:
- - Name of test material (as cited in study report): Vanady sulphate
- Molecular formula (if other than submission substance): VOSO4
- Supplier: Central Drug House, Delhi, India
- Analytical purity: no data
Constituent 1
Constituent 2
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Age at study initiation: adult
- Weight at study initiation: (P) Males: 170-200 g
- Housing: polypropylene cages
- Diet (e.g. ad libitum): pellet diet; ad libitum
- Water (e.g. ad libitum): water; ad libitum
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 - 28
- Photoperiod (hrs dark / hrs light): 12 / 12
Administration / exposure
- Route of administration:
- oral: drinking water
- Vehicle:
- water
- Details on mating procedure:
- - M/F ratio per cage: 1:2
- Length of cohabitation: 5 days starting on day 55 after begin of dosing
- Proof of pregnancy: vaginal plug / sperm in vaginal smear - Analytical verification of doses or concentrations:
- no
- Duration of treatment / exposure:
- 60 days
- Frequency of treatment:
- daily
Doses / concentrations
- Remarks:
- Doses / Concentrations:
100 mg/kg bw/d
Basis:
nominal conc.
- No. of animals per sex per dose:
- 7 males
- Control animals:
- yes, concurrent vehicle
Examinations
- Parental animals: Observations and examinations:
- CAGE SIDE OBSERVATIONS: No data
DETAILED CLINICAL OBSERVATIONS: No data
BODY WEIGHT: Yes
- Time schedule for examinations: prior to dosing and at the end of study - Sperm parameters (parental animals):
- Parameters examined in all male parental generations:
testis weight, epididymis weight, sperm count in testes, sperm density and motility, sperm morphology, seminiferous tubulues diameter, Leydig cell nucleidiameter - Litter observations:
- PARAMETERS EXAMINED
The following parameters were examined in F1 offspring: number of pups - Postmortem examinations (parental animals):
- SACRIFICE
- Male animals: All surviving animals
- Maternal animals: no data
GROSS NECROPSY
- Gross necropsy consisted of testes and accessory sex organs
HISTOPATHOLOGY / ORGAN WEIGHTS
The tissues were prepared for microscopic examination and weighed, respectively: testes, epididymides, semial vehicle, ventral prostate
BIOCHEMICHEICAL PARAMETERS:
Following parametes (in organs) were examined: protein (testes, cauda epididymides), sialic acid (testes, cauda epididymides, seminal vesicle), glycogen (testes, epdidymides), chloesterol (testes), fructose (seminal vesicle) - Statistics:
- Data were expressed as mean +/- SEM and the significance of difference was analyzed by the Student's t-test.
Results and discussion
Results: P0 (first parental generation)
Details on results (P0)
While control rats showed a significant increase in body weight, treated animals exhibited no body weight gain; instead a non-significant decrease in body weight was noted.
REPRODUCTIVE FUNCTION: SPERM MEASURES (PARENTAL ANIMALS)
Treated animals showed a significant decline in the cauda epididymal sperm density and motility.
REPRODUCTIVE PERFORMANCE (PARENTAL ANIMALS)
Treated animals showed a decline in fertility and litter size.
ORGAN WEIGHTS (PARENTAL ANIMALS)
Treated rats had a significant slight decrease in relative weight of testis and accessory sex organs.
HISTOPATHOLOGY (PARENTAL ANIMALS)
- A significant reduction in diameters of seminiferous tubules and Leydig cells nuclei compared to control animals was found in treated animals. In the testes of treated animals, exfoliation and degeneration of spermatogenic cells was found.
- A decline in post meiotic germ cells and spermatozoa in the lumen of the seminiferous tubules were noted.
BIOCHEMICAL OBSERVATIONS (PARENTAL ANIMALS)
- Protein and sialic acid contents of testis and cauda epididymis were significantly reduced in treated animals.
- Glycogen content of testis and epididymis was not changed in treated rats, while the cholesterol was significantly enhanced.
- Fructose content of the seminal vesicle was significantly reduced in treated rats.
Effect levels (P0)
open allclose all
- Dose descriptor:
- LOAEL
- Effect level:
- 100 mg/kg bw/day (nominal)
- Sex:
- male
- Basis for effect level:
- other: Changes in weight and biochemical paramters of reproductive organs; changes in sperm analysis and morphometry of reproductive organ tissue
- Dose descriptor:
- LOAEL
- Effect level:
- 189 mg/kg bw/day (nominal)
- Sex:
- male
- Basis for effect level:
- other: vanadyl pyrophosphate (corresponding dose)
Overall reproductive toxicity
- Reproductive effects observed:
- not specified
Any other information on results incl. tables
Body and organ weights:
Group | Initial | Final | Testes | Epididymides | Seminal vesicle | Ventral prostate |
Control | 180 ± 2.4 | 190.2 ± 2.7* | 1345 ± 43.74 | 580.33 ± 15.79 | 561.00 ± 15.47 | 302.20 ± 16.76 |
Vanadyl sulphate (100 mg/kg bw/d) | 185.1 ± 2.3 | 179.8 ± 4.25 | 1174 ± 50.60** | 505.24 ± 20.30** | 492.35 ± 18.20** | 246.82 ± 12.64** |
*p<0.05 compared with initial body weight; **p<0.05 compared with control rats
Cauda epididymal sperm analysis, fertility performance and morphometery:
Group | Sperm count (million/mm3) | Motility (%) | Fertility test (%) | Litter size | Seminiferous tubules diameter (µm) | Leydig cells nucleidiameter (µm) |
Control | 46.80 ± 2.50 | 74.40 ± 2.70 | 10/10 (100%) | 7.7 ± 0.70 | 270.00 ± 8.75 | 6.68 ± 0.30 |
Vanadyl sulphate (100 mg/kg bw/d) | 35.20 ± 1.85** | 42.0 ± 4.47*** | 5/10 (50%) | 5.0 ± 0.45** | 232.40 ± 7.75* | 5.40 ± 0.27* |
Fertility test: no. of females delivered / no. of females inseminated
*p<0.05, **p<0.01, ***p<0.001 compared to control
Tissue biochemical parameters:
Protein (mg/g) | Sialic acid (mg/g) | Glycogen (mg/g) | Cholesterol (mg/g) | Fructose (mg/g) | |||||
Group | Testis | Cauda epididymes | Testis | Cauda epididymes | Seminal vesicle | Testis | Epididymis | Testis | Seminal vesicle |
Control | 178.80 ± 8.16 | 205.62 ± 4.85 | 4.46 ± 0.22 | 5.11 ± 0.16 | 4.92 ± 0.22 | 3.12 ± 0.19 | 3.08 ± 0.18 | 5.66 ± 0.22 | 5.28 ± 0.28 |
Vanadyl sulphate (100 mg/kg bw/d) | 149.86 ± 6.67* | 172.25 ± 6.64** | 3.82 ± 0.17* | 4.22 ± 0.21* | 4.26 ± 0.26 | 3.59 ± 0.16 | 3.48 ± 0.21 | 7.19 ± 0.32** | 4.39 ± 0.23* |
*p<0.05, **p<0.01 compared with control
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.
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