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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
skin irritation / corrosion
Remarks:
in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Report date:
2015

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 431 (In Vitro Skin Corrosion: Human Skin Model Test)
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
3-acetyl-8,9,10,11-tetrahydro-5H-6-oxatetraphen-8-one
EC Number:
810-268-8
Cas Number:
1438383-92-6
Molecular formula:
C19H16O3
IUPAC Name:
3-acetyl-8,9,10,11-tetrahydro-5H-6-oxatetraphen-8-one
Test material form:
solid: particulate/powder
Remarks:
migrated information: powder

Test system

Duration of treatment / exposure:
3 minutes and 60 minutes at room temperature
Number of animals:
none

Results and discussion

Any other information on results incl. tables

Mean cell viability in the tissues treated with the test item was 109.156% at 3 minute exposure period and 94.292% at 60 minute exposure period. Significant reduction in cell viability was not observed at any of the exposure period in the treated tissues when compared with the concurrent negative control. Differences between the viability of treated tissues was less than 10% i.e. % CV.

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Under the specified experimental conditions, the test ite is concluded to be non-corrosive in in vitro skin corrosion test using reconstructed human epidermis (RHE) tissues.
Executive summary:

The test item has obligatory labelling requirement for skin irritation.