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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2002
Report date:
2002

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
Version / remarks:
version of 1996
Deviations:
no
GLP compliance:
yes
Test type:
acute toxic class method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Methylidynetri-p-phenylene triisocyanate
EC Number:
219-351-8
EC Name:
Methylidynetri-p-phenylene triisocyanate
Cas Number:
2422-91-5
Molecular formula:
C22H13N3O3
IUPAC Name:
1-[bis(4-isocyanatophenyl)methyl]-4-isocyanatobenzene

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female
Details on test animals or test system and environmental conditions:
SPF-bred Wistar rats of the strain HdsCpd:WU
TEST ANIMALS
- Source: Harlan Winkelmann GmbH, Borchen, Germany
- Age at study initiation: 8-9 weeks
- Weight at study initiation: 225-244 g (males) and 158-164 g (females)
- Fasting period before administration of test substance: about 17 h

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
corn oil
Doses:
2000 mg/kg
No. of animals per sex per dose:
3
Control animals:
no

Results and discussion

Effect levelsopen allclose all
Sex:
male/female
Dose descriptor:
discriminating dose
Effect level:
ca. 540 mg/kg bw
Based on:
act. ingr.
Remarks on result:
other: calculated from the LD50: > 2500 mg/kg (cut off) determined for the trade product (= a solution of 27% Triphenylmethane-4,4',4''-triisocyanate in ethyl acetate (w/w)
Sex:
male/female
Dose descriptor:
other: LD50 (cut off value)
Effect level:
> 2 500 mg/kg bw
Based on:
test mat.
Remarks on result:
other: a dose of 2000 mg/kg bw was tolerated without any findings
Mortality:
no deaths
Clinical signs:
other: none
Gross pathology:
no findings
Other findings:
none

Any other information on results incl. tables

Dose (mg/kg bw) Toxicological results  Onset and duration of signs  Onset of mortality
     male
 2000 0 / 0 / 3 --- --- 
          female
  2000   0 / 0 / 3  ---  ---

Toxicological results:

number of dead animals / number of animals with signs after treatment / number of animals treated

Applicant's summary and conclusion

Executive summary:

The acute oral toxicity of the Triphenylmethane-4,4',4''-triisocyanate (administered as a 27% solution in ethyl acetate) was evaluated in a GLP-compliant study on male and female Wistar rats according to OECD TG 423 of 1996. The oral dose of 2000 mg solution/kg bw was tolerated without mortalities, clinical signs, effects on weight gain or gross pathological findings. According to OECD TG 423 the LD50 cut-off of the solution can therefore be determined with > 2500 mg solution/kg bw. With regard to the content of Triphenylmethane-4,4',4''-triisocyanatet this is equivalent to approx. 540 mg/kg .