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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: dermal

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Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
disregarded due to major methodological deficiencies
Study period:
1980
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
significant methodological deficiencies
Remarks:
(i) test substance not moistened with water before application to skin, (ii) no information on housing and feeding conditions given, (iii) no clinical examinations, no pathology reported

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1992

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 402 (Acute Dermal Toxicity)
Deviations:
no
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Vanadium oxide sulphate
EC Number:
248-652-7
EC Name:
Vanadium oxide sulphate
Cas Number:
27774-13-6
Molecular formula:
VOSO4
IUPAC Name:
oxovanadium(2+) sulfate
Test material form:
solid: particulate/powder
Remarks:
migrated information: powder
Details on test material:
no data

Test animals

Species:
rabbit
Strain:
New Zealand White
Sex:
female
Details on test animals or test system and environmental conditions:
no further information

Administration / exposure

Type of coverage:
occlusive
Vehicle:
unchanged (no vehicle)
Details on dermal exposure:
- The area of the animal was covered with gauze and dental dam. The entire midsection was then wrapped in elastoplast tape.
- The test substance was removed after 24h of exposure.
Duration of exposure:
24 hours
Doses:
3150 mg/kg bw, 3970 mg/kg bw, 5000 mg/kg bw
No. of animals per sex per dose:
5
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- No necropsy of survivors were not performed, other examinations were not performed
Statistics:
LD50 values were determined using the moving average method of Weil.
Weil, C.S. (1952) Tables for convenient calculation of median effective dose (LD50 or ED50) and instructions in their use. Biometrics 8: 249-263

Results and discussion

Effect levels
Sex:
female
Dose descriptor:
LD50
Effect level:
4 450 mg/kg bw
Based on:
test mat.
Remarks on result:
other: confidence limits could not be calculated due to lack of partial mortalities
Mortality:
Dose 3150 mg/kg bw.: 0 animals
Dose 3970 mg/kg bw.: 0 animals
Dose 5000 mg/kg bw.: 3 animals
Clinical signs:
other: no data
Gross pathology:
no data
Other findings:
no data

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
LD50 (female, rabbit): 4450 mg/kg bw (vanadium oxide sulphate)
According to the EC-Regulation 1272/2008 and subsequent regulations, vanadium oxide sulphate should not be classified.