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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Repeated dose toxicity: inhalation

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Administrative data

Endpoint:
short-term repeated dose toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
other: Does not meet important criteria of today standard methods.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1971
Report date:
1971

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
The vapour of the test substance was blown into the experimental enclosure of 0.4 m3.  The rats weighed 172-182 g, and 20 were used. The rats were observed daily, weighed weekly, and clinically examined at the end of the exposure.  Blood samples from 5 rats were examined, and liver and kidney function tests were conducted on groups of 5 rats. At the end of the exposure the rats were anaesthetized with ether, and bled to death.  The dissected animals were macroscopically examined.  Various organs of the killed rats were weighed.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Diaminotoluene
EC Number:
246-910-3
EC Name:
Diaminotoluene
Cas Number:
25376-45-8
Molecular formula:
C7H10N2
IUPAC Name:
3-methylbenzene-1,2-diamine
Details on test material:
2,4/2,6-Toluylendiamine (80/20)

Test animals

Species:
rat
Strain:
Wistar
Sex:
male

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
whole body
Vehicle:
other: unchanged (no vehicle)
Analytical verification of doses or concentrations:
yes
Duration of treatment / exposure:
28 days
Frequency of treatment:
4 hr/day, 5 consecutive days/week
Doses / concentrations
Remarks:
Doses / Concentrations:
0, 0.083 mg/l.
Basis:
analytical conc.
No. of animals per sex per dose:
20 for dose group; animal number of control group not given
Control animals:
yes, sham-exposed

Results and discussion

Effect levels

Dose descriptor:
LOAEC
Effect level:
0.083 mg/L air (analytical)
Sex:
male

Target system / organ toxicity

Critical effects observed:
not specified

Any other information on results incl. tables

At a concentration of 0.083 mg/l (83 mg/m3) the exposed rats were similar to the

controls in appearance and condition. The exposed rats had reduced body weight

gain. The blood tests showed that the exposed rats had relative lymphopenia. The

liver and kidney function tests were normal. Dissection of the killed rats did 

not find any compound related changes. The liver, kidney, and thyroid/body weight

ratios were increased.


In another similar study using a concentration of 0.0095 mg 2,4/2,6-TDA/l (9.5 mg/m3) the treated rats did not significantly differ from the control animals.

Applicant's summary and conclusion