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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1996
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study well documented, meets generally accepted scientific principles, acceptable for assessment

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1996
Reference Type:
publication
Title:
Robust summary and test plan for 1,5-cyclooctadiene with cover letter dated 11 Dec 2002
Author:
DuPont Safety, Health & Environmental Excellence Center, Wilmington (Del., USA)
Year:
2002
Bibliographic source:
Quelle U.S. EPA 37 pp

Materials and methods

Principles of method if other than guideline:
Method: other: See Test Conditions: standard acute inhalation toxicity study; nose-only
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Cycloocta-1,5-diene
EC Number:
203-907-1
EC Name:
Cycloocta-1,5-diene
Cas Number:
111-78-4
Molecular formula:
C8H12
IUPAC Name:
(1Z,5Z)-cycloocta-1,5-diene
Details on test material:
Test substance: other TS: 1,5-cyclooctadiene, purity > 99%

Test animals

Species:
rat
Strain:
other: Crl:CD(R) BR
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ORGANISMS: 
- Source: 
- Age: approximately 8 weeks
- Weight at study initiation: 268-292 g
- Number of animals: 6
- Controls: no

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
nose only
Vehicle:
other: houseline air
Details on inhalation exposure:
ADMINISTRATION: 
- Type of exposure: single nose-only exposure
- Concentrations: measured at approximately 15-minute intervals by GC
- Type or preparation of particles: No particles. Chamber atmospheres  were generated by vaporizing the test substance in a heated nitrogen  stream  and dilution with houseline air.
- Temperature, humidity in chamber: 23 +/- 2 °C, 50 +/- 10 %
Analytical verification of test atmosphere concentrations:
yes
Remarks:
Concentrations was measured at approximately 15-minute intervals by GC
Duration of exposure:
4 h
Concentrations:
1400, 2700, or 4300 ppm = 6.30, 12.1, or 19.3 mg/l
No. of animals per sex per dose:
6
Control animals:
no
Details on study design:
EXAMINATIONS:
mortality and response to stimuli during exposure; clinical  signs and mortality immediately following exposure; body weight and  clinical signs daily 
thereafter for 14 days (during weekends only when  warranted by the health status of the rats). 
Statistics:
Evaluation with simple  statistics at p <= 0.05.

Results and discussion

Effect levels
Key result
Sex:
male
Dose descriptor:
other: ALC (approximate lethal concentration)
Effect level:
ca. 12 - ca. 19 mg/L air
Exp. duration:
4 h
Mortality:
- 1400 ppm: 0/6
- 2700 ppm: 1/6 night after exposure
- 4300 ppm: 4/6 during exposure 
Clinical signs:
other: - Response to external sound stimuli: Absent for all animals after 3  hours exposure - Immobility: 2 surviving rats at 4300 ppm and 4 rats at 2700 ppm - Ataxia: 3 rats at 1400 ppm - Ocular discharge, ruffled fur, or stained perineum: Up to 4 days  follow
Body weight:
Body weights: Losses of 4-14% were recorded the day after exposure,  followed by body weight gains in all animals.
Gross pathology:
no data
Other findings:
no other findings

Any other information on results incl. tables

no further results

Applicant's summary and conclusion

Conclusions:
Under the present test conditions, test item is considered slightly toxic in an acute inhalation toxicity study.
Executive summary:

Three groups of 6 male rats each were exposed nose-only for a single, 4 hour period to vapors of the test item in air at chamber vapor concentrations of 1400, 2700 or 4300 ppm. Mortality was 0/6, 1/6 and 4/6 at 1400, 2700 and 4300 ppm respectively. By 3 hours into the exposure all rats failed to respond to external sound stimuli. At the end of exposure, the 2 rats at 4300 ppm and 4 rats at 2700 ppm were immobile. Threee rats at 1400 ppm exhibited ataxia. Other clinical signs of toxicity observed after exposure: ocular discharge,  lethargy, irregular respiration. Ocular discharge, ruffled fur or stained perineum were observed up

to 4 days following exposure.

On an acute inhaltion basis, test item is considered slightly toxic.