Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2006

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: 92/69/EWG, B.3; OECD 402 (1992)
GLP compliance:
yes
Limit test:
yes

Test material

Constituent 1

Test animals

Species:
other: rat, Crl:CD(SD)

Administration / exposure

Type of coverage:
semiocclusive
Vehicle:
other: deionisiertes Wasser
Duration of exposure:
24 h

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Mortality:
Male: 5000 mg/kg bw; Number of animals: 5; Number of deaths: 0
Female: 5000 mg/kg bw; Number of animals: 5; Number of deaths: 0
Clinical signs:
other: Signs of toxicity related to dose levels: Systemische Toxizitäten oder Gewichtsverlust traten nicht auf.
Gross pathology:
Effects on organs:
Es wurden keine Effekte beobachtet.
Other findings:
Signs of toxicity (local):
Es wurden keine Hautreaktionen beobachtet.

Todesfälle traten nicht auf.

Applicant's summary and conclusion

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