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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
short-term repeated dose toxicity: dermal
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: no guideline study but menteiond in peer-reviewed publication

Data source

Referenceopen allclose all

Title:
Unnamed
Year:
1968
Reference Type:
secondary source
Title:
1,4-Dichlor-2-nitrobenzol
Author:
BUA
Year:
1991
Bibliographic source:
BUA-Stoffbericht 65, ISBN 3-527-28462-1, VChVerlagsgesellschaft mbH, 8940 Weinheim

Materials and methods

Test guideline
Guideline:
other: guideline not mentioned
Principles of method if other than guideline:
once daily for 15 days dermal application of different doses to the shaved back of female rabbits
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
1,4-dichloro-2-nitrobenzene
EC Number:
201-923-3
EC Name:
1,4-dichloro-2-nitrobenzene
Cas Number:
89-61-2
Molecular formula:
C6H3Cl2NO2
IUPAC Name:
1,4-dichloro-2-nitrobenzene
Test material form:
other: solid
Details on test material:
no data

Test animals

Species:
rabbit
Strain:
other:
Sex:
female
Details on test animals or test system and environmental conditions:
no data

Administration / exposure

Type of coverage:
not specified
Vehicle:
not specified
Details on exposure:
once daily dermal application of different doses to the shaved back of groups of 5 female rabbits
Analytical verification of doses or concentrations:
not specified
Details on analytical verification of doses or concentrations:
no data
Duration of treatment / exposure:
up to 15 days (see dosing scheme in details on study design)
Frequency of treatment:
once daily
Doses / concentrations
Remarks:
Doses / Concentrations:
100, 200, 400 mg/kg bw/day
Basis:

No. of animals per sex per dose:
up to 5 females per dose see dosing scheme in details on study design
Control animals:
not specified
Details on study design:
100 mg/kg bw was applied to 5 animals on 15 days
200 mg/kg bw was applied to 5 animals on 3 days
200 mg/kg bw was applied to 5 animals on 15 days
400 mg/kg bw was applied to 5 animals on 10 days
400 mg/kg bw was applied to 5 animals on 11 days
400 mg/kg bw was applied to 5 animals on 12 days
Positive control:
no data

Examinations

Observations and examinations performed and frequency:
molrality clinidal signs and hematology
Sacrifice and pathology:
macroscopic evaluation
Statistics:
no data

Results and discussion

Results of examinations

Details on results:
Mortality:
100 mg/kg bw was applied to 5 animals on 15 days: 0/5
200 mg/kg bw was applied to 5 animals on 3 days: 1/5
200 mg/kg bw was applied to 5 animals on 15 days 1/5
400 mg/kg bw was applied to 5 animals on 10 days: 5/5
400 mg/kg bw was applied to 5 animals on 11 days: 5/5
400 mg/kg bw was applied to 5 animals on 12 days: 5/5

dose depending decreae of erythrocytes and hemoglobin; urinary discoloration
no histopathololgical changes in heart lung kidney adremal liver
spleen of the animals dosed with 400 mg/kg bw showed hyperemy,deposition of pigment and increased erythropoiesis

Effect levels

open allclose all
Dose descriptor:
NOAEL
Remarks on result:
not determinable
Remarks:
no NOAEL identified
Dose descriptor:
LOAEL
Effect level:
100 mg/kg bw/day
Sex:
female
Basis for effect level:
other: based on dose -depending impairment of blood picture (no details)

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion