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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: other routes
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Basic data given (few informations, investigated for dose finding only)

Data source

Reference
Reference Type:
publication
Title:
Vergleichende Kanzerogenese Versuche mit 2,4-Toluylendiamin, 2,4/2,6-Toluylendianin 80/20, m-Phenylendiamin, o-Toluidin, p-Toluidin, 4,4'-Diaminodiphenylnethan, Benzidin, bei subkutaner Applikation an Ratten
Author:
Bayer AG, Steinhoff D, Dycka
Year:
1981
Bibliographic source:
Unpublished report No 10682, July 06, 1981

Materials and methods

Principles of method if other than guideline:
dose finding for a cancerogenicity study
GLP compliance:
no
Remarks:
GLP was not mandatory at the time of the study

Test material

Constituent 1
Chemical structure
Reference substance name:
o-toluidine
EC Number:
202-429-0
EC Name:
o-toluidine
Cas Number:
95-53-4
Molecular formula:
C7H9N
IUPAC Name:
2-methylaniline
Details on test material:
- Name of test material (as cited in study report): o-toludine
- Analytical purity: > 99%

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
female

Administration / exposure

Route of administration:
subcutaneous
Vehicle:
peanut oil

Results and discussion

Effect levels
Sex:
female
Dose descriptor:
LD50
Effect level:
1 115 mg/kg bw
95% CL:
984 - 1 295

Applicant's summary and conclusion