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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1985
Report date:
1986

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
1,3,5-triisopropylbenzene
EC Number:
211-941-3
EC Name:
1,3,5-triisopropylbenzene
Cas Number:
717-74-8
Molecular formula:
C15H24
IUPAC Name:
1,3,5-tris(propan-2-yl)benzene

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Doses:
1250, 2500, 5000 mg/kg
No. of animals per sex per dose:
5
Control animals:
no

Results and discussion

Effect levelsopen allclose all
Sex:
male
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Based on:
test mat.
Sex:
female
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Based on:
test mat.

Applicant's summary and conclusion

Interpretation of results:
relatively harmless
Remarks:
Migrated information Criteria used for interpretation of results: expert judgment
Conclusions:
No adverse clinical signs at doses as high as 5000 mg/kg
Executive summary:

Five male and 5 female sprague dawley rats were used to assess the acute oral toxicity of 1,3,5 -triisopropylbenzene (TIPB). Single doses of 1250, 2500, and 5000 mg/kg were administered via oral gavage, and rats were observed for up to 14 days following treatment. No adverse clinical signs at doses as high as 5000 mg/kg. From these data, it was concluded that TIPB is relatively harmless.