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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2004
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
2008
Report date:
2008

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
not specified
GLP compliance:
yes
Test type:
acute toxic class method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
p-toluic acid
EC Number:
202-803-3
EC Name:
p-toluic acid
Cas Number:
99-94-5
Molecular formula:
C8H8O2
IUPAC Name:
4-methylbenzoic acid
Test material form:
solid: crystalline

Test animals

Species:
rat
Strain:
Crj: CD(SD)
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
CMC (carboxymethyl cellulose)
Doses:
0(vehicle), 1000, 1500, 2000 mg/kg bw
No. of animals per sex per dose:
Five males and five females were assigned to each dose.

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Mortality:
No deaths occurred during the study.
Clinical signs:
other: One female was observed with temporary loose stool at 2000 mg/kg bw. No clinical signs were observed in the animals given 1000 and 1500 mg/kg bw.
Gross pathology:
No macroscopic abnormalities were observed at autopsy for any doses in either sex.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The result of acute oral toxicity LD50 >2000 mg/kg bw results in a not classified verdict.