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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
eye irritation: in vitro / ex 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
Year:
2018

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 492 (Reconstructed Human Cornea-like Epithelium (RhCE) Test Method for Identifying Chemicals Not Requiring Classification and Labelling for Eye Irritation or Serious Eye Damage)
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Reference substance name:
Liquidambar Styraciflua, oil
EC Number:
946-732-2
IUPAC Name:
Liquidambar Styraciflua, oil

Test animals / tissue source

Species:
other: Reconstructed human Cornea-like Epithelium

Test system

Vehicle:
unchanged (no vehicle)
Controls:
yes, concurrent positive control
yes, concurrent negative control
Amount / concentration applied:
50 μl to 0.6 cm2 RhCE
Duration of treatment / exposure:
30 min
Duration of post- treatment incubation (in vitro):
12 min + 120 min
Number of animals or in vitro replicates:
2

Results and discussion

In vitro

Results
Irritation parameter:
other: Viability(%)
Value:
105.92
Vehicle controls validity:
not applicable
Negative controls validity:
valid
Positive controls validity:
valid

Applicant's summary and conclusion

Interpretation of results:
other: not classified
Conclusions:
Under the test conditions applied, the substance is considered as no category.