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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Carcinogenicity

Currently viewing:

Administrative data

Endpoint:
carcinogenicity: oral
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
1978
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Short report, non-GLP, early study, one sex only;

Data source

Reference
Reference Type:
publication
Title:
Testing of twenty-one environmental aromatic amines or derivatives for long-term toxicity or carcinogenicity
Author:
Weisburger, E.K. et al.
Year:
1978
Bibliographic source:
J. Environ. Pathol. Toxicol. 2: 325-356 (1978)

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Animals were fed a diet containing the test material for 18 months. Afterwards they were observed for and additional recovery period and subsequently killed and tissues examined histopathologically.
GLP compliance:
no
Remarks:
pre-dates GLP

Test material

Constituent 1
Chemical structure
Reference substance name:
1-chloro-2,4-dinitrobenzene
EC Number:
202-551-4
EC Name:
1-chloro-2,4-dinitrobenzene
Cas Number:
97-00-7
Molecular formula:
C6H3ClN2O4
IUPAC Name:
1-chloro-2,4-dinitrobenzene
Details on test material:
purity: 97 - 99 %, commercial sample

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Charles River
- Age at study initiation: 4 - 6 weeks

- Food: Standard diet ad libitum
- aclimation period: 2 weeks
- housing: groups of 5

Administration / exposure

Route of administration:
oral: feed
Vehicle:
not specified
Details on exposure:
Stability in feed over 3 days was determined via extraction and chemical identification/quantification
Analytical verification of doses or concentrations:
not specified
Duration of treatment / exposure:
18 months
Frequency of treatment:
daily
Post exposure period:
6 months
Doses / concentrationsopen allclose all
Remarks:
Doses / Concentrations:
low
Basis:
other: 1000 ppm(diet, nominal) for 2 months; 250 for 3 months; 500 for 13 months; recovery for 6 months
Remarks:
Doses / Concentrations:
high
Basis:
other: 2000 (diet, nominal) for 2 months; 500 for 3 months; 1000 for 13 months; recovery for 6 months
No. of animals per sex per dose:
25
Control animals:
yes, plain diet
Details on study design:
The dose level was changed several times due to observed/ no-observed effects on body weight
Positive control:
not required

Examinations

Observations and examinations performed and frequency:
CAGE SIDE OBSERVATIONS: No data

DETAILED CLINICAL OBSERVATIONS: Yes / No / No data
- Time schedule:


BODY WEIGHT: Yes
- Time schedule for examinations: no data ("carefully")


FOOD CONSUMPTION AND COMPOUND INTAKE (if feeding study):
- Food consumption for each animal determined and mean daily diet consumption calculated as g food/kg body weight/day: No data
- Compound intake calculated as time-weighted averages from the consumption and body weight gain data: No data


FOOD EFFICIENCY:
- Body weight gain in kg/food consumption in kg per unit time X 100 calculated as time-weighted averages from the consumption and body weight gain data: No data


WATER CONSUMPTION AND COMPOUND INTAKE (if drinking water study): No data
- Time schedule for examinations:


OPHTHALMOSCOPIC EXAMINATION: No data

HAEMATOLOGY:No data

CLINICAL CHEMISTRY: No data

URINALYSIS: No data

NEUROBEHAVIOURAL EXAMINATION: No data
Sacrifice and pathology:
GROSS PATHOLOGY: Yes ; only in animals surviving > 6 months
HISTOPATHOLOGY: Yes : but no details reported

Results and discussion

Results of examinations

Clinical signs:
not specified
Mortality:
not specified
Body weight and weight changes:
effects observed, treatment-related
Food consumption and compound intake (if feeding study):
not specified
Food efficiency:
not specified
Water consumption and compound intake (if drinking water study):
not specified
Ophthalmological findings:
not specified
Haematological findings:
not specified
Clinical biochemistry findings:
not specified
Urinalysis findings:
not specified
Behaviour (functional findings):
not specified
Organ weight findings including organ / body weight ratios:
not specified
Gross pathological findings:
effects observed, treatment-related
Histopathological findings: non-neoplastic:
effects observed, treatment-related
Histopathological findings: neoplastic:
effects observed, treatment-related
Details on results:
1-Chloro-2,4-dinitrobenzene was not tumorigenic in rats
Relevance of carcinogenic effects / potential:
The study provided no indication of an influence of the testmaterial on tumor incidence in male rats.

Effect levels

Dose descriptor:
NOAEL
Effect level:
ca. 1 028 ppm (nominal)
Sex:
male
Basis for effect level:
other: Although the dose level was changed due to (missing) effects on body weight, no details were reported
Remarks on result:
other: Effect type: carcinogenicity (migrated information)

Applicant's summary and conclusion

Conclusions:
1-Chloro-2,4-dinitrobenzene was not tumorigenic in rats