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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Data from study report

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2001

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: as per mentioned below
Principles of method if other than guideline:
Acute Oral toxicity study was conducted on rats
GLP compliance:
no
Test type:
other: Not reported

Test material

Constituent 1
Chemical structure
Reference substance name:
p-anisidine
EC Number:
203-254-2
EC Name:
p-anisidine
Cas Number:
104-94-9
Molecular formula:
C7H9NO
IUPAC Name:
4-methoxyaniline
Details on test material:
- Name of test material: 4-methoxyaniline
- Molecular formula: CH3OC6H4NH2
- Molecular weight: 123.15 g/mol
- Substance type: Organic
- Physical state: Solid

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
Not reported

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
not specified
Details on oral exposure:
Not reported
Doses:
Not reported
No. of animals per sex per dose:
Not reported
Control animals:
not specified
Details on study design:
Not reported
Statistics:
Not reported

Results and discussion

Preliminary study:
Not reported
Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
1 400 mg/kg bw
Based on:
test mat.
Remarks on result:
other: The observed effects were hematologic changes , anemia and nephrotoxicity
Mortality:
Not reported
Clinical signs:
Not reported
Body weight:
Not reported
Gross pathology:
Not reported
Other findings:
Not reported

Applicant's summary and conclusion

Interpretation of results:
Toxicity Category IV
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The acute oral LD50 in rats after oral exposure to 4 methoxyaniline in 1400mg/kgw
Executive summary:

Acute Oral toxicity study was conducted on rats.

The rats were orally dosed with the test chemical and effects were observed

The observed effects were hematologic changes , anemia and nephrotoxicity

The acute oral LD50 in rats after oral exposure to 4 methoxyaniline in 1400mg/kgw