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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: dermal
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:
1986
Report date:
1986

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 402 (Acute Dermal Toxicity)
GLP compliance:
yes
Test type:
standard acute method
Limit test:
yes

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:
guinea pig
Strain:
Hartley
Sex:
male/female

Administration / exposure

Type of coverage:
occlusive
Vehicle:
unchanged (no vehicle)
Details on dermal exposure:
A limit dose of 20 ml/kg was applied to 5 male and 5 female guinea pigs The backs of the guinea pigs were clipped and the material was applied to the entire back area under occlusion created by application of a woven pad and a rubber dental dam over the application site. The material was left in contact with the skin for 24 hours, then washed off. Animals were assessed for skin irritation upon patch removal and for the next few days. Dermal toxicity and lethality were assessed by recording any clinical signs which subsequently evolved over a period of 10 days. As with the oral studies, weight loss was considered a sign of toxicity and an indication of absorption of the test chemical. The validity of these studies rests on the fact that, even though few animals were tested, the exposure regimen was far in excess of current guidelines. For example, for dermal toxicity, the current limit dose is 2000 mg/kg, applied for 24 hours; using the Kodak method, the 20 gm/kg dose used was 10 times greater than is currently recommended. Therefore, the exposure regimen in the Kodak studies used up to 40 times more material applied six times longer. This resulted in an exposure 240 times more severe than currently required in skin irritation studies conducted using international Guidelines.
Duration of exposure:
24 hours
Doses:
5, 10, 20 ml/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:
> 20 mL/kg bw
Based on:
test mat.
Sex:
female
Dose descriptor:
LD50
Effect level:
> 20 mL/kg bw
Based on:
test mat.
Mortality:
none observed
Clinical signs:
other: slight to moderate erythema was observed on days 1-3.

Applicant's summary and conclusion

Interpretation of results:
relatively harmless
Remarks:
Migrated information Criteria used for interpretation of results: expert judgment
Conclusions:
Acute dermal LD50 for 1,3,5-triisopropylbenzene (TIPB) for both male and female guinea pigs was determined to be greater than 20 mL/kg.
Executive summary:

Acute dermal toxicity of 1,3,5 -triisopropylbenzene (TIPB) was evaluated in guinea pigs using a limit dose of 20 mL/kg. Hair was clipped from the back of 5 male and 5 female guinea pigs, and TIPB was applied to the entire back under an occlusive dressing for 24 hours and then washed off. There was no mortality observed during the course of this study, and therefore the acute oral LD50 for TIPB is considered to be > 20 mL/kg for both male and female guinea pigs.