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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
24.04.1985 - 27.04.1985
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: The study was conducted in GLP compliance and according to an OECD guideline.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1985
Report date:
1985

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
GLP compliance:
yes

Test material

Constituent 1
Reference substance name:
3,5-Diacetoxyacetophenon
IUPAC Name:
3,5-Diacetoxyacetophenon
Details on test material:
Charge: 96
Analysenattest vom 10.01.1984

Test animals / tissue source

Species:
rabbit
Strain:
Himalayan
Details on test animals or tissues and environmental conditions:
TEST ANIMALS
- Source: Fa. Dr. Karl Thomae GmbH, Biberach/Riss
- Age at study initiation: ca. 8 Monate
- Weight at study initiation: ca. 2 kg
- Housing: Einzelhaltung in Drahtkäfigen
- Diet (e.g. ad libitum): Kaninchenzuchtfutter
- Water (e.g. ad libitum): ad libitum


Test system

Vehicle:
unchanged (no vehicle)
Controls:
no
Amount / concentration applied:
20 mg
Observation period (in vivo):
1 h, 24 h, 48 h und 72 h nach der Verabreichung
Number of animals or in vitro replicates:
2 males and 2 females

Results and discussion

In vivo

Results
Irritation parameter:
overall irritation score
Basis:
mean
Time point:
other: 72 h
Score:
0

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Es wurde bei allen Tieren eine leichte
Rötung der Konjunktiva eine Stunde post
appl. beobachtet. Nach 24 Stunden waren
diese Veränderungen verschwunden.
Die Substanz 3,5-Diacetoxyacetophenon wird
deshalb als schleimhautverträglich beurteilt.