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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2008
Report date:
2008

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
EU Method B.3 (Acute Toxicity (Dermal))
Qualifier:
according to guideline
Guideline:
OECD Guideline 402 (Acute Dermal Toxicity)
Version / remarks:
2002
GLP compliance:
yes (incl. QA statement)
Test type:
other: Acute dermal toxicity
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
3-bromo-5-chlorophenol
EC Number:
611-435-6
Cas Number:
56962-04-0
Molecular formula:
C6H4BrClO
IUPAC Name:
3-bromo-5-chlorophenol

Test animals

Species:
rat
Strain:
Crj: CD(SD)
Sex:
male/female
Details on test animals or test system and environmental conditions:
Charles River Laboratories, Research Models and Services, Germany GmbH, Sanhofer Weg 7, 97633 Sulzfeld, Germany
Body weight: (at dosing) Males: 208-227 g; Female: 200-219 g
Age: (at dosing) Males: 51 days; Females: 65 days

Administration / exposure

Type of coverage:
occlusive
Vehicle:
other: Sesame oil
Details on dermal exposure:
Hair on the site of applicatiom was clipped with a hair clipper 24 hrs before administration.
The test item suspension was applied to 8 layers of gauze.
The gauze was covered with plastic sheet.
Duration of exposure:
24 hours
Doses:
1 Doses - 2000 mg/kg b.w.
No. of animals per sex per dose:
5 male and 5 female
Details on study design:
Observation of skin reactions, changes in body weight clinical signs and necropsy were performed.

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Remarks on result:
other: 24h - > 2000 mg/kg; 14 days - > 2000 mg/kg
Mortality:
none
Clinical signs:
none
Body weight:
Males: 208-227 g
Female: 200-219 g
Gross pathology:
no findings at necopsy
Other findings:
no skin reactions

Applicant's summary and conclusion

Interpretation of results:
Category 5 based on GHS criteria
Remarks:
Migrated information
Conclusions:
Under the present test conditions, a single dermal application of 2000 mg/kg b.w. to rats did not reveal any clinical signs of toxicity. No influence on animal behaviour or premature mortality was noted. The body wight gain was not influenced. No skin reactions were observed at the application site. The macroscopic examination did not reveal any changes.