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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: inhalation

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Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
migrated information: read-across based on grouping of substances (category approach)
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable, well-documented study report which meets basic scientific principles. Test substance purity not given.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1989
Report date:
1989

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 403 (Acute Inhalation Toxicity)
Deviations:
yes
Remarks:
purity of test substance not given, 10 male and female animals used per test group, 5 males and females sacrificed one day after exposure, only 2 concentrations were tested
GLP compliance:
not specified
Test type:
standard acute method

Test material

Constituent 1
Reference substance name:
Bis(tridecyl) adipate
EC Number:
241-029-0
EC Name:
Bis(tridecyl) adipate
Cas Number:
16958-92-2
IUPAC Name:
ditridecyl adipate
Details on test material:
- Name of test material (as cited in study report): only trade name given
- Physical state: liquid
- Analytical purity: not given
- Expiration date of the lot/batch: 01-01-1990
- Storage condition of test material: room temperature under ventilation

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female

Administration / exposure

Route of administration:
inhalation: aerosol
Type of inhalation exposure:
whole body
Vehicle:
air
Analytical verification of test atmosphere concentrations:
yes
Remarks:
Gas Chromatography
Duration of exposure:
4 h
Concentrations:
0.5, 5.0 mg/L (3.2 mg/L was the highest practical concentration which could be achieved, as determined by analytical verification instead of 5 mg/L)
No. of animals per sex per dose:
10 (5 animals of each sex sacrificed one day after exposure)
Control animals:
yes

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 3.2 mg/L air (analytical)
Based on:
test mat.
Exp. duration:
4 h

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
DSD: not classified
CLP: not classified