[No public or meaningful name is available]

Repeated dose toxicity: oral

Administrative data

Endpoint:

short-term repeated dose toxicity: oral

Remarks:

combined repeated dose and reproduction / developmental screening

Type of information:

experimental study

Adequacy of study:

other information

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: No GLP defined

Cross-reference

Reason / purpose for cross-reference:

reference to same study

Data source

Reference

Reference Type:

publication

Title:

Unnamed

Year:

1996

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

OECD Guideline 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test)

GLP compliance:

not specified

Limit test:

no

Test material

Test material information

Constituent 1

Reference substance name:

1,3-dichloro-4-nitrobenzene

EC Number:

210-248-3

EC Name:

1,3-dichloro-4-nitrobenzene

Cas Number:

611-06-3

Molecular formula:

C6H3Cl2NO2

IUPAC Name:

2,4-dichloro-1-nitrobenzene

Details on test material:

Purity: 98.0 %

Test animals

Species:

rat

Strain:

Crj: CD(SD)

Sex:

male/female

Administration / exposure

Route of administration:

oral: gavage

Vehicle:

corn oil

Analytical verification of doses or concentrations:

not specified

Duration of treatment / exposure:

Males, 45 days
Females, from 14 days before mating to day 3 of lactation

Frequency of treatment:

no data

Doses / concentrations

Remarks:

Doses / Concentrations:
0 (Vehicle), 8, 40, 200 mg/kg/day
Basis:
other: vehicle: corn oil

No. of animals per sex per dose:

Males: 12; Females: 12/group

Control animals:

yes

Results and discussion

Results of examinations

Clinical signs:

effects observed, treatment-related

Mortality:

mortality observed, treatment-related

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:

effects observed, treatment-related

Clinical biochemistry findings:

effects observed, treatment-related

Urinalysis findings:

effects observed, treatment-related

Behaviour (functional findings):

not specified

Organ weight findings including organ / body weight ratios:

effects observed, treatment-related

Gross pathological findings:

effects observed, treatment-related

Histopathological findings: non-neoplastic:

effects observed, treatment-related

Histopathological findings: neoplastic:

effects observed, treatment-related

Effect levels

Dose descriptor:

NOEL

Effect level:

< 8 mg/kg bw/day (nominal)

Sex:

male/female

Target system / organ toxicity

Critical effects observed:

not specified

Any other information on results incl. tables

There were no abnormal clinical signs attributable to the administration of the test substance, although, one female rat given 200 mg/kg died during delivery. The body weight gain of females given 200 mg/kg was lower than that of the controls during the gestation period.

Hematological examination revealed decreases in red blood cells in males given 8 mg/kg or more, decreases in hematocrit and hemoglobin, increases in reticulocytes, and slight anemia in males given 40 and 200 mg/kg. Blood clinical examination revealed increases in total protein, albumin and gamma-GTP and decreases in creatinine in males given 40 and 200 mg/kg. Total bilirubin and the A/G ratio were increased in males given 200 mg/kg. Absolute and relative liver and kidney weights showed increase or a tendency for increase in both sexes given 200 mg/kg. necropsy revealed enlargement of the liver in both sexes given 200 mg/kg, and enlargement of kidneys in males given 200 mg/kg. Other treatment-related gross findings included atrophy of the thymus and enlargement of the adrenal glands in treated females.

Histopathological examination revealed swelling and single cell necrosis of liver cells in both sexes given 200 mg/kg. Moreover, mitosis of liver cells were observed in males given 200 mg/kg. The slight increase in the incidence of hyaline droplets of the renal tubules in males and basophilic change of the renal tubules in females, both given 200 mg/kg, were also noted in a few females given 8 mg/kg or more, and necrosis of the renal tubules was observed in a few females given 40 and 200 mg/kg. A variety of lesions including a moderate degree of pigment deposit in the spleen, atrophy of the thymus, swelling of the liver cells, ulcer action in the stomach, duodenum and large intestine, single liver cell necrosis and fibrosis of the renal tubular epithelium, were observed in females that delivered all stillborn pups and in females where all pups died, in the group given 200 mg/kg. Counting of numbers of spermatogenic cells at stage VIII in the testes from control males and males given 200 mg/kg revealed no treatment-related effects.

Applicant's summary and conclusion

Executive summary:

The test substance was studied for oral toxicity in an OECD combined repeat dose and reproductive/developmental toxicity screening test at doses of 0, 8, 40 and 200 mg/kg/day. With regard to repeat dose toxicity, one female rat given 200 mg/kg died during delivery. Body weight gain of females given 200 mg/kg was lower than that of controls during the gestation period. hematological examination showed decreases of red blood cells in males given 8 mg/kg or more, as well as decreases of hematocrit and hemoglobin, increases of reticulocytes, and slight anemia in males given 40 and 200 mg/kg. Blood chemical examination revealed increases in total protein, albumin and y-GTP and decreases in creatinine in males given 40 and 200 mg/kg. Increases in total bilirubin and A/G ratio were also observed in males given 200 mg/kg. Absolute and relative weights of the liver and kidneys showed increases or a tendency for increase in both sexes given 200 mg/kg and mg/kg. As gross findings, enlargement of the liver was observed in both sexes given 200 mg/kg and enlargement of the kidneys in males given 200 mg/kg. Histopathologial examination revealed swelling and single cell necrosis of liver cells in both sexes given 200 mg/kg. Moreover, mitosis of liver cells were observed in the liver of males given 200 mg/kg. The slight increase in the incidence of hyaline droplets of renal tubules in males and basophilic change of the renal tubules in females, both given 200 mg/kg, were also noted in a few females given 8 mg/kg or more, and necrosis of the renal tubules was observed in a few females given 40 and 200 mg/kg.

The author declared 8 mg/kg as LOEL, because slight effects on red blood cells in male rats (red blood counts: control 7.98 mg/kg; 8 mg/kg= 7.79 mg/kg) and histopathology were observed, but the effects on red blood cells were isolated effects and no other effects were observed.

Basophile changes (contol group= 1 rat; 8 mg/kg= 2 rats; 40 mg/kg= 1 rat; 200 mg/kg 5 rats) The results were not dose related and no signifficant effect was seen in the 8 mg/kg group of female rats

Because the effects were not seen as advers the LOEL = NOAEL of 8 mg/kg.