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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1996-10-29 to 1996-11-15
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Guideline study OECD 405, OECD 1981; updated guideline, adopted 1987-02-24. Deviation: The purity of the test substance is not mentioned

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1996
Report date:
1996

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
Deviations:
no
GLP compliance:
yes

Test material

Constituent 1
Reference substance name:
Perfluoralkyljodid 612
IUPAC Name:
Perfluoralkyljodid 612
Details on test material:
- Molecular formula (if other than submission substance): C2F5(C2F4)nJ; (n= 2-5)
- Molecular weight (if other than submission substance): 530g/mol
- Physical state: violet fluid
- Analytical purity: n/a
- Impurities (identity and concentrations): n/a
- Composition of test material, percentage of components: n/a
- Lot/batch No.: P.96029
- Expiration date of the lot/batch: 1998-07-16
- Storage condition of test material: darkness at room temperature in a fume cupboard

Test animals / tissue source

Species:
rabbit
Strain:
New Zealand White

Test system

Vehicle:
unchanged (no vehicle)
Controls:
not required
Duration of treatment / exposure:
24h after application eyes were rinsed with isotonic saline at approx. 37°C
Observation period (in vivo):
1, 24, 48 and 72 hours after application of the test substance.
Number of animals or in vitro replicates:
3

Results and discussion

In vivo

Results
Irritation parameter:
overall irritation score
Basis:
mean
Remarks:
#1, #2, #3
Time point:
other: 24h, 48h and 72h after application of test substance
Score:
0
Max. score:
0
Remarks on result:
other: none

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Based on the test results the test substance is not irritating to the eye