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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
skin irritation: 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
Year:
1990
Report date:
1990

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
1,4-dichloro-2-(1,1,2,3,3,3-hexafluoropropoxy)-5-nitrobenzene
EC Number:
620-459-6
Cas Number:
130841-23-5
Molecular formula:
C9H3Cl2F6NO3
IUPAC Name:
1,4-dichloro-2-(1,1,2,3,3,3-hexafluoropropoxy)-5-nitrobenzene
Details on test material:
- Test article: CGA 230672 techn.
- Purity test date: 97,3 %
- Lot/batch No.: P. 906005

Test animals

Species:
rabbit
Strain:
New Zealand White
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Dr. K Thomae GmbH, Chemisch-pharmazeutische Fabrik
- Age at study initiation: 9 - 13 weeks old
- Weight at study initiation: 2700 - 2880 g
- Housing: individually in metal cages
- Diet (e.g. ad libitum): yes (standart rabbit pellet, Nafag No. 814)
- Water (e.g. ad libitum): yes
- Acclimatisation period: at least 5 days


ENVIRONMENTAL CONDITIONS
- Temperature (°C): ca. 20 °C
- Humidity (%): 30 - 70 %
- Photoperiod (hrs dark / hrs light): 12

Test system

Type of coverage:
occlusive
Preparation of test site:
shaved
Vehicle:
unchanged (no vehicle)
Duration of treatment / exposure:
4 hours
Observation period:
skin reactions were evaluated 1, 24, 48 and 72 hours after removing the gauze patches.
The animals were checked daily for systemic symptoms and mortality.
Number of animals:
3 male rabbits
Details on study design:
TEST SITE
- Area of exposure: gauze patch (ca. 12-16 cm²) bearing 0,5 ml of the test article was applied to the right flank of each animal.
- coverage: the patches were loosely covered with an aluminium foil (ca. 36 cm²)

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
mean
Time point:
other: 24 - 72 hours
Score:
0.33
Max. score:
2
Reversibility:
fully reversible
Remarks:
until the end of the observation period on day 3
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 24 - 72 hours
Score:
0
Max. score:
0
Reversibility:
fully reversible
Remarks:
until the end of the observation period on day 3
Irritant / corrosive response data:
non-irritant

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU