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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:
key study
Study period:
1980
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Secondary source

Data source

Reference
Reference Type:
review article or handbook
Title:
Toxikologische Bewertung – p-Aminophenol.
Author:
Berufsgenossenschaft der chemischen Industrie BCI, Heidelberg, Germany
Year:
1995
Bibliographic source:
Toxicological Evaluation, 15, 337-381

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
EPA OPPTS 870.1200 (Acute Dermal Toxicity)
GLP compliance:
not specified
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
4-aminophenol
EC Number:
204-616-2
EC Name:
4-aminophenol
Cas Number:
123-30-8
Molecular formula:
C6H7NO
IUPAC Name:
4-aminophenol

Test animals

Species:
rabbit
Strain:
New Zealand White
Sex:
not specified

Administration / exposure

Type of coverage:
occlusive
Vehicle:
other: tragacanth
Details on dermal exposure:
TEST SITE
- Area of exposure: dorsal skin (clipped hair)
TEST SITE
- Area of exposure: intact and abraded skin


TEST MATERIAL
- Concentration (if solution): 50% aqueous suspension with tragacanth
Duration of exposure:
24 hr
Doses:
2000. 4000 and 8000 mg/kg bw
No. of animals per sex per dose:
4 animals per dose
Control animals:
not specified
Details on study design:
- Duration of observation period following administration: 14 days

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 8 000 mg/kg bw
Mortality:
All animals survived.
Clinical signs:
other: Deep green-brown discoloration of application site was observed, which later changed to yellowish-brown.
Gross pathology:
No. effect was observed.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU