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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP and guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1995
Report date:
1995

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
GLP compliance:
yes (incl. QA statement)
Remarks:
testing lab.

Test material

Constituent 1
Chemical structure
Reference substance name:
Trifluoro(tetrahydrofuran)boron
EC Number:
207-325-9
EC Name:
Trifluoro(tetrahydrofuran)boron
Cas Number:
462-34-0
Molecular formula:
C4H8BF3O
IUPAC Name:
trifluoro(oxolan-1-ium-1-yl)boranuide
Details on test material:
Name of the test substance used in the study report: Borfluorid-Tetrahydrofuran
Lot No. 5/93

Test animals

Species:
rabbit
Strain:
New Zealand White
Details on test animals or test system and environmental conditions:
Young adult rabbits were used. They were singly housed in stainless wire mesh cages (no bedding) in fully air-conditioned rooms with a temperature of 20 - 24°C and a relative humidity of 30 - 70%. The day/night rhythm was 12 hours dark and 12 hours light. The animals were offered a standardized rabbit laboratory diet (130 g/animal/day) as well as tap water (ca. 130 g/animal/day).
The acclimatization period was at least 1 week. Body weight determination was done shortly before application of the test substance.

Test system

Type of coverage:
semiocclusive
Preparation of test site:
other: the fur was removed by clipping the dorsal of the trunk of the animal
Vehicle:
unchanged (no vehicle)
Controls:
other: untreated skin of the same animal
Amount / concentration applied:
0.5 ml
Duration of treatment / exposure:
3 minutes, 1 hour
Observation period:
3-min exposure: 72 hours
1-hour exposure: 24 hours
Number of animals:
3 (3-min exposure); 1 (1-h exposure)
Details on study design:
Application site: upper third of the back or flanks
Application volume: The test patches (2.5 x 2.5 cm) were moistened with 0.5 ml of the liquid test substance.
Readings were done 1 h, 24 h, 48 h and 72 h after removal of the test patches.
A check for general observations and for any dead or moribund animal(s) was made twice each working day and once on weekendes and public holidays.
Additional investigation: Because the visual assessment of the skin did not allow a statement with respect to the depth of necrotic changes, a cross incision of the trated skin has been performed after the rabbit was killed at study termination.

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
mean
Time point:
other: 24 - 72 h
Score:
0.2
Max. score:
4
Reversibility:
fully reversible within: 72 hours
Remarks on result:
other: 3-min application
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 24 - 48 h
Score:
0
Max. score:
4
Remarks on result:
other: 3-min application
Irritation parameter:
edema score
Basis:
animal #1
Time point:
other: 24 h
Score:
4
Max. score:
4
Reversibility:
other: not determined due to study termination after 24 h
Irritant / corrosive response data:
1-hour application: The average score for irritation could not be calculated because of visual necrosis and therefrom resulting study termination 24 hours after removal of the test patch.
Other effects:
The necrotic change of the skin was assessed by macroscopic pathology indicating full-thickness necrosis.

Applicant's summary and conclusion

Interpretation of results:
corrosive
Remarks:
Migrated information