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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: other routes

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Administrative data

Endpoint:
acute toxicity: other routes
Type of information:
experimental study
Adequacy of study:
weight of evidence
Study period:
1986
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1968

Materials and methods

Principles of method if other than guideline:
The test item was applied intraperitoneally to the stomach in pure form and all treated animals were observed for 14 days after the administration.
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
α,α,α-trifluorotoluene
EC Number:
202-635-0
EC Name:
α,α,α-trifluorotoluene
Cas Number:
98-08-8
Molecular formula:
C7H5F3
IUPAC Name:
α,α,α-trifluorotoluene

Test animals

Species:
mouse
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 25 - 30 g

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
unchanged (no vehicle)
No. of animals per sex per dose:
6 mice per dose
Details on study design:
- Duration of observation period following administration: 14 days

Results and discussion

Effect levels
Key result
Sex:
not specified
Dose descriptor:
LD50
Effect level:
10 000 mg/kg bw
Based on:
test mat.
95% CL:
>= 7 642 - <= 13 400
Mortality:
No mortality was reported.
Clinical signs:
No signs of toxicity were reported.

Applicant's summary and conclusion

Conclusions:
The oral LD50 to mice was determined to be 10000 mg/kg bw.
Executive summary:

In a published study, the test item was applied intraperitoneally to the stomach of mice in pure form and all treated animals were observed for 14 days after the administration. The LD50 was determined to be 10000 mg/kg bw.