Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
sub-chronic toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: only secondary literature

Data source

Referenceopen allclose all

Reference Type:
other: ECHA disseminated dossier
Title:
ECHA disseminated dossier
Year:
2014
Bibliographic source:
ECHA disseminated dossier
Report date:
2014
Reference Type:
secondary source
Title:
not applicable
Author:
not applicable
Year:
2008
Bibliographic source:
GESTIS-database on hazardous substances - Information system on hazardous substances of the German Social Accident Insurance

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Rats and guinea pigs were exposed to vapors and aerosols of trifluoroacetic acid for 4 hrs/day during 5 or 4 months.
GLP compliance:
not specified
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Trifluoroacetic acid
EC Number:
200-929-3
EC Name:
Trifluoroacetic acid
Cas Number:
76-05-1
Molecular formula:
C2HF3O2
IUPAC Name:
trifluoroacetic acid

Test animals

Species:
other: rats and guinea pigs
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
other: inhalation of vapours and aerosols
Type of inhalation exposure:
not specified
Vehicle:
not specified
Remarks on MMAD:
MMAD / GSD: no data
Analytical verification of doses or concentrations:
not specified
Duration of treatment / exposure:
4 hrs/day for 5 months (rats) or 4 months (guinea pigs)
Frequency of treatment:
6 times a week
Doses / concentrationsopen allclose all
Remarks:
Doses / Concentrations:
0.4-0.7 mg/L (guinea pigs)
Basis: no data
Remarks:
Doses / Concentrations:
0.025-0.05 mg/L (rats)
Basis: no data
No. of animals per sex per dose:
48 rats (12 served as control) or 30 guinea pigs (10 served as control).
Control animals:
yes

Results and discussion

Effect levels

open allclose all
Dose descriptor:
LOAEL
Effect level:
< 0.05 mg/L air
Based on:
test mat.
Sex:
not specified
Basis for effect level:
other: LOAEL (rat): severe signs of irritation on the respiratory pathway and the eyes, effects in the liver and kidney, and body weight loss.
Dose descriptor:
LOAEL
Effect level:
< 0.7 mg/L air
Based on:
test mat.
Sex:
not specified
Basis for effect level:
other: LOAEL (guinea pig): severe signs of irritation on the respiratory pathway and the eyes, effects in the liver and kidney, and body weight loss.

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion