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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Remarks:
read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
guideline study
Justification for type of information:
The toxicity observed in this study is most likely caused by the relatively high reactivity of the diiodofluoroalkane. The PDA-3 is smaller than the primary components of the PDA-4,6 mixture, and the dediiodination reaction most likely occurs at somewhat faster rate than the PDA-4,6, but the reaction occurs in both. Because of this, the data for PDA-3 is a conservative estimation of the toxicity resulting from PDA-4,6 and so it is reasonable to read across to it.
Cross-reference
Reason / purpose for cross-reference:
read-across source

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2015
Report date:
2015

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 403 (Acute Inhalation Toxicity)
Deviations:
yes
Remarks:
Initials were on the first page of each chromatogram but were not on every page. This deviation does not adversely impact the study as the operator(s) was clearly identified on the first page of the chromatograms generated for the day.
GLP compliance:
yes
Test type:
traditional method

Test material

Constituent 1
Reference substance name:
Reference substance 001
Cas Number:
422-91-3
Test material form:
liquid
Details on test material:
- Purity: Not reported
- CAS: 422-91-3

Test animals

Species:
rat
Strain:
other: Crl:CD (SD)
Sex:
male/female

Administration / exposure

Route of administration:
inhalation: mixture of vapour and aerosol / mist
Type of inhalation exposure:
nose only
Vehicle:
air
Remark on MMAD/GSD:
1.22 µm for the 0.92 mg/L exposure/4.74 µm
2.45 µm for the 2.9 mg/L exposure/4.02
2.17 µm for the 4.8 mg/L exposure/3.84
2.40 µm for the 5.3 mg/L exposure/3.71
2.18 µm for the 16 mg/L exposure/3.79
Duration of exposure:
4 h
Concentrations:
0.93 mg/L (0.92 mg/L vapor and 0.0074 mg/L aerosol)
2.9 mg/L (2.9 mg/L vapor and 0.013 mg/L aerosol)
4.8 mg/L (4.8 mg/L vapor and 0.023 mg/L aerosol)
5.3 mg/L (5.3 mg/L vapor and 0.022 mg/L aerosol
16 mg/L (16 mg/L vapor and 0.057 mg/L aerosol
No. of animals per sex per dose:
5 males and 5 females
Control animals:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
4.5 mg/L air
Based on:
test mat.
95% CL:
> 3.5 - < 5.3
Exp. duration:
4 h

Applicant's summary and conclusion

Interpretation of results:
Category 3 based on GHS criteria
Conclusions:
4-hour LC50 = 4.5 mg/L
Executive summary:

An acute inhalation toxicity study was conducted in accordance with OECD Guideline 403. Under the conditions of this study, the 4-hour inhalation median lethal concentration (LC50) for the test substance in male and female rats was 4.5 mg/L total atmospheric concentration with 95% confidence limits at 3.5-5.3 mg/L.