Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Genetic toxicity: in vitro

Currently viewing:

Administrative data

Endpoint:
in vitro gene mutation study in bacteria
Remarks:
Type of genotoxicity: gene mutation
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: scientifically acceptable and well documented - but only 4 strains tested

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1982
Report date:
1982

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Principles of method if other than guideline:
1,8-naphthylenediamine was investigated using the Salmonella/microsome test (Ames Test) for point mutagenic effects in doses up to 12500 µg per plate on four Salmonella typhimurium LT2 mutants. These comprised the histidine-auxotrophic strains TA 1535, TA 100, TA 1537 and TA 98.
GLP compliance:
not specified
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
1,8-naphthylenediamine
EC Number:
207-529-8
EC Name:
1,8-naphthylenediamine
Cas Number:
479-27-6
Molecular formula:
C10H10N2
IUPAC Name:
naphthalene-1,8-diamine
Details on test material:
content: 96.6%

Method

Species / strain
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Additional strain / cell type characteristics:
other: all strains are partly deficient in lipopolysaccharide side chains
Metabolic activation:
with and without
Metabolic activation system:
S-9 mix
Test concentrations with justification for top dose:
first test: 0, 20, 100, 500, 2500, 12500 µg/plate
repeat test: 0, 0,8, 4, 20, 100, 500 µg/plate
Controls
Untreated negative controls:
yes
Negative solvent / vehicle controls:
yes
True negative controls:
not specified
Positive controls:
yes
Positive control substance:
other: endoxan, trypaflavin, 2-aminoanthracen

Results and discussion

Test results
Species / strain:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Metabolic activation:
with and without
Genotoxicity:
positive
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
at 500 µg with and without S-9 mix
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Remarks on result:
other: other: S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Remarks:
Migrated from field 'Test system'.

Any other information on results incl. tables

The test substance revealed a mutagenic effect on S. typhimurium strains TA 98, TA100 and TA1537. The lowest reproducible and effective doses for S. typhimurium TA 98, TA 100. and TA 1537 were 20 µg/plate.

1,8 -Naphthylenediamine is positive under the conditions of this Ames test with and without metabolic activation.

Applicant's summary and conclusion

Conclusions:
Interpretation of results:
positive
Executive summary:

1,8-Naphthylenediamine was investigated using the Salmonella/microsome test (Ames Test) for point mutagenic effects in doses up to 12500 µg per plate on four Salmonella typhimurium LT2 mutants. These comprised the histidine-auxotrophic strains TA 1535, TA 100, TA 1537 and TA 98.

The test substance revealed a mutagenic effect on S. typhimurium strains TA 98, TA100 and TA1537. The lowest reproducible and effective doses for S. typhimurium TA 98, TA 100. and TA 1537 were 20 µg/plate.

1,8 -Naphthylenediamine is positive under the conditions of this Ames test with and without metabolic activation.