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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable study report which meets basic scientific principles.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1958
Report date:
1958

Materials and methods

Principles of method if other than guideline:
BASF-Test

Before OECD Guideline 405 was established, eye irritation was tested using an internal method (BASF test). White Vienna rabbits were used. 0.1 g of the test substance was applied to the conjunctival sac of the right eye of the animal. The adjacent eye was treated with one drop of physiological solution of sodium chloride and served as a control. The animals were observed several times on the treatment day and 8 days afterwards, and findings were recorded on working days.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Tetrachlorophthalic anhydride
EC Number:
204-171-4
EC Name:
Tetrachlorophthalic anhydride
Cas Number:
117-08-8
Molecular formula:
C8Cl4O3
IUPAC Name:
tetrachloro-1,3-dihydro-2-benzofuran-1,3-dione
Details on test material:
- Name of test material (as cited in study report): Tetrachlorophthalic anhydride
- Analytical purity: no data

Test animals / tissue source

Species:
rabbit
Strain:
Vienna White
Details on test animals or tissues and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 2.83-3.32 kg

Test system

Vehicle:
unchanged (no vehicle)
Controls:
other: The adjacent eye was treated with one drop of physiological solution of sodium chloride and served as a control.
Amount / concentration applied:
0.1 g
Duration of treatment / exposure:
8 days
Observation period (in vivo):
8 days
Number of animals or in vitro replicates:
2
Details on study design:
SCORING SYSTEM: The original BASF grading was converted into the numerical grading according to the OECD Draize system.


Results and discussion

Any other information on results incl. tables

One hour after application of the test substance slight erythema, secretion, residues of test substance and a film on the cornea was reported for both animals. 24 hours after application of the test substance, secretion, corneal opacity, slight erythema, and slight edema was reported for both animals. On day 2, only slight erythema was left in one animal, which reversed fully until day 8.

Animal

Readings

Cornea

Conjunctivae (Redness)

01

24 h

2

1

48 h

0

1

02

24 h

3-4

1

48 h

0

1

Applicant's summary and conclusion