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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: Acceptable well documented report which meets basic scientific principles.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1961
Report date:
1961

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
BASF-Test:
Standardised study to determine the acute toxicity of the test item in male and female mice after single i.p. application (observation period: 14 days).
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Reference substance name:
p-Xylidinbase
IUPAC Name:
p-Xylidinbase
Details on test material:
- Name of test material (as cited in study report): p-Xylidinbase; 4,4'-Diamino-2,2',5,5'-tetramethyldiphenylmethan
no further data

Test animals

Species:
mouse
Strain:
not specified
Sex:
male/female

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
other: aequeous solution with traganth
Doses:
100, 200, 400, 800 mg/kg bw
No. of animals per sex per dose:
- 100 mg/kg bw: 10
- 200 mg/kg bw: 10
- 400 mg/kg bw: 10
- 800 mg/kg bw: 10
Control animals:
yes
Details on study design:
- Duration of observation period following administration: 14 days
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 800 mg/kg bw
Based on:
test mat.
Mortality:
- 800 mg/kg bw: 2/10,

Clinical signs:
- 400 and 800 mg/kg bw: slight stagger; apathy, adbominal position

Body weight:
no data
Gross pathology:
no data

Applicant's summary and conclusion