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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: inhalation

Currently viewing:

Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Precedes establishment of guidelines and GLP. Documentation is limited.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1963
Report date:
1963

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 433 draft (Acute Inhalation Toxicity: Fixed Concentration Procedure) (not officially approved)
GLP compliance:
not specified
Test type:
fixed concentration procedure
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Benzophenone-3,3':4,4'-tetracarboxylic dianhydride
EC Number:
219-348-1
EC Name:
Benzophenone-3,3':4,4'-tetracarboxylic dianhydride
Cas Number:
2421-28-5
Molecular formula:
C17H6O7
IUPAC Name:
5-(1,3-dioxo-1,3-dihydro-2-benzofuran-5-carbonyl)-1,3-dihydro-2-benzofuran-1,3-dione
Constituent 2
Reference substance name:
291-348-1
IUPAC Name:
291-348-1
Test material form:
solid: crystalline

Test animals

Species:
rat
Strain:
Wistar
Sex:
male

Administration / exposure

Route of administration:
inhalation: dust
Type of inhalation exposure:
whole body
Vehicle:
clean air
Details on inhalation exposure:
stainless steel inhalation chamber, 1530 L. Total air flow through the system was 50 liters per minute. The actual chamber concentration was not determined during the exposure. The mean theoretical concentration was calulated from the air flow and net loss of material was 4.72 mg per liter.
Analytical verification of test atmosphere concentrations:
no
Duration of exposure:
6 h
Control animals:
no
Details on study design:
During the exposure, all animals were continuously observed for mortality and toxic effects. Following exposures, the animals were group-housed in metal cages suspended above droppings. Food and water were freely available during the pre-exposure period of adjustment to the laboratory environment and the post-exposure period. During the 14 day post-exposure period, the animals were observed daily for possible latent effects. Necropsies were performed following the sacrifice of the test animals at the termination of the study.
Statistics:
no data

Results and discussion

Effect levels
Key result
Sex:
male
Dose descriptor:
LC0
Effect level:
4.44 mg/L air (nominal)
Based on:
test mat.
Exp. duration:
6 h
Remarks on result:
other: No deaths
Mortality:
no deaths
Clinical signs:
other: Slight evidence of lung damage such as foci of consolidation were noted at time of necropsy. As these were also noted in control animals, they were not considered to be related to the test material.

Applicant's summary and conclusion

Interpretation of results:
study cannot be used for classification
Remarks:
Migrated information
Conclusions:
1,3-Isobenzofurandione, 5,5'-carbonylbis- (BTDA) was tested for acute inhalation lethality in rats in a protocol similar to OECD 433. No deaths or adverse effects occurred at concentrations of 4.44 mg/L.