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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Skin sensitisation

Currently viewing:

Administrative data

Endpoint:
skin sensitisation
Remarks:
in vivo
Type of information:
experimental study
Adequacy of study:
weight of evidence
Study period:
1973
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable, well documented publication/study report which meets basic scientific principles

Data source

Reference
Reference Type:
publication
Title:
Experimentelle Untersuchung der allergenen Wirkung von Ortho- und Para-nitrochlorbenzol.
Author:
Rusakov NV, Korotkova GI, Biklubatov VS (1973)
Year:
1973
Bibliographic source:
Gig Sanit 3: 13-16

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
3 drops (10 % sol.) to the clipped area of the skin; 22nd day inj. of Freund-adjuvans and TS into the hind paw (0.5 mg/kg bw), d28 1 drop (10 % sol.) to an untreated clipped area of the skin; reading time not mentioned
GLP compliance:
no
Type of study:
other: modified Freunds complete adjuvant test

Test material

Constituent 1
Chemical structure
Reference substance name:
1-chloro-4-nitrobenzene
EC Number:
202-809-6
EC Name:
1-chloro-4-nitrobenzene
Cas Number:
100-00-5
Molecular formula:
C6H4ClNO2
IUPAC Name:
1-chloro-4-nitrobenzene
Details on test material:
- Name of test material (as cited in study report): Para-nitrochlorbenzol
- Analytical purity: no data

In vivo test system

Test animals

Species:
guinea pig
Strain:
not specified
Sex:
not specified

Study design: in vivo (non-LLNA)

Inductionopen allclose all
Route:
other: epicutaneous, no more informations
Vehicle:
other: acetone
Concentration / amount:
10% in acetone
Challengeopen allclose all
Route:
other: epicutaneous, no more informations
Vehicle:
other: acetone
Concentration / amount:
10% in acetone
No. of animals per dose:
10
Details on study design:
1st application: Induction 10 % 2nd application: Challenge 10 %
Positive control substance(s):
not specified

Study design: in vivo (LLNA)

Statistics:
no data

Results and discussion

Any other information on results incl. tables

No more data given

Applicant's summary and conclusion

Interpretation of results:
sensitising
Remarks:
Migrated information