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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
in vivo mammalian somatic cell study: cytogenicity / erythrocyte micronucleus
Type of information:
read-across based on grouping of substances (category approach)
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Justification for type of information:
Octafluoropropane is a gas, making testing difficult. However, saturated perfluorocarbons have very similar toxicological properties and so a "read across" approach is justified.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1984
Report date:
1984

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 474 (Mammalian Erythrocyte Micronucleus Test)
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
Perfluoroperhydrophenanthrene
EC Number:
400-470-0
EC Name:
Perfluoroperhydrophenanthrene
Cas Number:
306-91-2
Molecular formula:
C14F24
IUPAC Name:
1,1,2,2,3,3,4,4,4a,4b,5,5,6,6,7,7,8,8,8a,9,9,10,10,10a-Tetracosafluorophenanthrene
Test material form:
liquid

Test animals

Species:
mouse
Strain:
Swiss
Details on species / strain selection:
Specific Pathogen Free CD-1
Sex:
male/female
Details on test animals or test system and environmental conditions:
Kept i disposable plastic cages, maintained at 22degC, 30 changes of air per hour; free access to Spratt's Laboratory Diet Number 1 and tap water.

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
1% methyl cellulose
Details on exposure:
2026 mg/ml of test material was used, to give a total dose of 40520 mg/kg
Duration of treatment / exposure:
Single dose
Frequency of treatment:
Single dose
Post exposure period:
72 hours
Doses / concentrations
Dose / conc.:
40 520 mg/kg bw (total dose)
No. of animals per sex per dose:
15
Control animals:
yes, concurrent vehicle
Positive control(s):
Mitomycin C (by intraperitoneal injection).

Examinations

Tissues and cell types examined:
Bone marrow smears taken at 24, 48 and 72 hours examined for micronuclei
Evaluation criteria:
Ratio of polychromatic to normochromatic erythrocytes.
Statistics:
At least 1000 erythrocytes from each animal.

Results and discussion

Test results
Key result
Sex:
male/female
Genotoxicity:
negative
Toxicity:
no effects
Vehicle controls validity:
valid
Negative controls validity:
not applicable
Positive controls validity:
valid

Applicant's summary and conclusion

Conclusions:
Octafluoropropane is not genetically toxic
Executive summary:

Octafluoropropane is not genetically toxic