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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2003
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
other: Body responsible for the test
Title:
Unnamed

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: EEC B1 tris (OECD 423)
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
-
EC Number:
457-830-5
EC Name:
-
Cas Number:
2557-13-3
Molecular formula:
Hill formula: C9 H7 F3 O2
IUPAC Name:
Methyl, 3-Trifluoromethylbenzoate

Test animals

Species:
other: Rat Wistar CrlGIxBrlHan:WI
Strain:
Wistar

Administration / exposure

Vehicle:
other: Olive oil Ph.Eur./DAB

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 300 - < 2 000 mg/kg bw
Mortality:
Female: 2000 mg/kg bw; Number of animals: 3; Number of deaths: 3
Female: 300 mg/kg bw; Number of animals: 3; Number of deaths: 0
Clinical signs:
Signs of toxicity related to dose levels:
Clinical observation in the 2000 mg/kg administration group
revealed impaired and poor general state, dyspnoea,
staggering and smeared fur and were observed from hour 1
until including study day 1 after administration.


No clinical signs and findings were observed in the 300
mg/kg administration during clinical examination.
Gross pathology:
Effects on organs:
During necropsy the animals (2000 mg/kg, 3 females) that
died comprised a moderate post mortal state, few to many
black erosion /ulcers in the glandular stomach and a red
discoloration of the contents fo the urinary bladder. One
animal showed no macroscopic pathologic abnormalities.

No macroscopic pathologic abnormalities were seen in the
animals examinated at termination of the study (300 mg/kg, 6
females).

Applicant's summary and conclusion

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