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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
dermal absorption in vitro / ex vivo
Type of information:
other: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
secondary literature
Remarks:
The study is conducted on a read across test material. The complete read across justification is attached in section 13. The reliability of the original study is 4.

Data source

Reference
Reference Type:
secondary source
Title:
Unnamed
Year:
2004

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: Draft OECD Guideline (1996)
Principles of method if other than guideline:
Percutaneous absorption in vitro (400 – 900 μm thickness skin from porcine ears)

Test material

Constituent 1
Reference substance name:
Similar Substance 1
IUPAC Name:
Similar Substance 1

Results and discussion

Total recovery:
The mean recovery was 93.3% ± 4.05% (SD) in experiment I, and 115,2% ± 6.43% (SD) in experiment II.
Percutaneous absorption
Time point:
24 h
Dose:
5 mg
Remarks on result:
other: No absorption observed

Any other information on results incl. tables

Any measurable permeation through skin was not detected (Limit of detection: 5.5 - 5.7 μg/cm2 in

the two experiments, equivalent to 0.09-0.12% of the applied total amount.)

Applicant's summary and conclusion