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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
eye irritation: in vitro / ex vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
18/08/2016 -
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2016
Report date:
2016

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 437 (Bovine Corneal Opacity and Permeability Test Method for Identifying Ocular Corrosives and Severe Irritants)
Qualifier:
according to guideline
Guideline:
other: OECD Guideline 160 (Bovine Corneal opacity and permeability (BCOP) and isolated chicken eye (ICE) Test methods:collection of tissues for histological evaluation and collection of data on non-sever irritants)
Qualifier:
according to guideline
Guideline:
other: Regulation EU N.1152/2010 amending Regulation No.440/2008 EU-Method B.47
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
9β,11β-epoxy-17,21-dihydroxy-16β-methylpregna-1,4-diene-3,20-dione
EC Number:
213-563-4
EC Name:
9β,11β-epoxy-17,21-dihydroxy-16β-methylpregna-1,4-diene-3,20-dione
Cas Number:
981-34-0
Molecular formula:
C22H28O5
IUPAC Name:
17,21-dihydroxy-16-methyl-9,11-epoxypregna-1,4-diene-3,20-dione
Test material form:
solid: particulate/powder

Test animals / tissue source

Details on test animals or tissues and environmental conditions:
SOURCE OF COLLECTED EYES
- Source: bovine cornea collected from freshly slaughtered cattle
- Characteristics of donor animals (e.g. age, sex, weight): 12-60 months old
- Storage, temperature and transport conditions of ocular tissue (e.g. transport time, transport media and temperature, and other conditions): The eyes were transported to the test facility in Hank's balanced salt solution (supplemented with 0.01% streptomycin and 0.01% penicilin). Then, the corneas were dissected and incubated in medium at 32+/-1°C in an incubation chamber for 1 h.

Test system

Vehicle:
Hank's balanced salt solution
Duration of treatment / exposure:
Exposure time on the corneas was 3 hours and 55 minutes at 32+/- 1°C.
Duration of post- treatment incubation (in vitro):
The chambers were incubated for 85 min at 32 +/- 1°C.

Results and discussion

In vitro

Results
Irritation parameter:
in vitro irritation score
Vehicle controls validity:
valid
Negative controls validity:
valid
Positive controls validity:
valid
Remarks on result:
no indication of irritation

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
Under the conditions of this test, the test item Beta-Methylepoxy showed no effects on the cornea of the bovine eye. the calculated IVIS (in vitro irritancy score) is 1.17.
According to OECD Guideline no.437 (Jul.2013), a substance with an IVIS ≤ 3 requires no classification for eye irritation or serius eye damage.
The negative control (HBSS-solution) and the positive control (20% imidazole solution) have met the validity criteria.
No observations were made which might cause doubts concerning the validity of the study outcome. The test is considered valid.