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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

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Administrative data

Endpoint:
in vitro gene mutation study in bacteria
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
test procedure in accordance with generally accepted scientific standards and described in sufficient detail
Justification for type of information:
one of several accessible publications that are available in scientific literature

Data source

Reference
Reference Type:
publication
Title:
Chemically-induced unscheduled DNA synthesis in primary rat hepatocyte cultures: A comparison with bacterial mutagenicity using 218 compounds
Author:
Gregory S. Probst
Robert E. McMahon
L. E. Hill
Christina Z. Thompson
J. K. Epp
S. B. Neal
Year:
1981
Bibliographic source:
Probst, G. S., McMahon, R. E., Hill, L. E., Thompson, C. Z., Epp, J. K. and Neal, S. B. (1981), Environ. mutagen, 3: 11-32.

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
GLP compliance:
not specified
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
2-naphthol
EC Number:
205-182-7
EC Name:
2-naphthol
Cas Number:
135-19-3
Molecular formula:
C10H8O
IUPAC Name:
2-naphthol
Test material form:
solid
Specific details on test material used for the study:
Aldrich Chemical Co, Milwaukee, Wisconsin

Method

Species / strainopen allclose all
Species / strain / cell type:
S. typhimurium, other: G46
Species / strain / cell type:
S. typhimurium TA 1535
Species / strain / cell type:
S. typhimurium, other: TA1000
Species / strain / cell type:
S. typhimurium, other: C3076
Species / strain / cell type:
S. typhimurium TA 1537
Species / strain / cell type:
S. typhimurium, other: D3052
Species / strain / cell type:
S. typhimurium TA 1538
Species / strain / cell type:
S. typhimurium TA 98
Species / strain / cell type:
E. coli WP2
Species / strain / cell type:
E. coli WP2 uvr A
Metabolic activation:
with and without
Metabolic activation system:
S9
Details on test system and experimental conditions:
Bacterial mutagenesis was measured by a modification of the Ames test utilizing concentration gradient plates as described by McMahon et al. Briefly, inocula of ten bacterial tester strains were streaked across square agar plates containing a concentration gradient of test compound and mutagenicity was scored by noting the number of tester strains showing mutant colonies over a given concentration range. The test was conducted using eight histidine auxotrophs of Salmonella typhimurium (G46, TA1535, TAlOOO, C3076, TA1537, D3052, TA1538, and TA98) and two tryptophan auxotraphs of Escherichia coli (WP2 and WP2 uvrA-). Each compound was incorporated into four gradient plates to give a tenfold concentration range per plate, thus providing a 10,000-fold concentration range for the test. For metabolic activation, an S9 fraction, derived from the livers of Aroclor 1254 pretreated rats, was mixed with appropriate co-factors and included in an agar overlay on the gradient plates. Each compound was tested with and without metabolic activation. The data reported here include the number and identity of tester strains showing revertant colonies as well as an estimate of the minimal chemical concentration which produced revertants in the most sensitive tester strain.

Results and discussion

Test resultsopen allclose all
Key result
Species / strain:
S. typhimurium, other: G46
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Key result
Species / strain:
S. typhimurium TA 1535
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Key result
Species / strain:
S. typhimurium, other: TA1000
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Key result
Species / strain:
S. typhimurium, other: C3076
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Key result
Species / strain:
S. typhimurium TA 1537
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Key result
Species / strain:
S. typhimurium, other: D3052
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Key result
Species / strain:
S. typhimurium, other: TA1538
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Key result
Species / strain:
S. typhimurium TA 98
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Key result
Species / strain:
E. coli WP2
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Key result
Species / strain:
E. coli WP2 uvr A
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified

Applicant's summary and conclusion

Conclusions:
2-Naphthol was not mutagenic in a bacterial reverse mutation test (see Probst, G. S., McMahon, R. E., Hill, L. E., Thompson, C. Z., Epp, J. K. and Neal, S. B. (1981), Chemically-induced unscheduled DNA synthesis in primary rat hepatocyte cultures: A comparison with bacterial mutagenicity using 218 compounds. Environ. mutagen, 3: 11-32.)
Executive summary:

2-Naphthol was not mutagenic in several Ames-tests using Salmonella typhimurium strains TA 98, TA100, TA 1535, TA 1537, TA 1538, G46, C3076, D3052, and Escherichia coli WP2uvrA, both in the presence and in the absence of metabolic activation (liver S-9 mix) and including cytotoxic concentrations (Probst et al., 1981; Purchase et al., 1978; Muzall and Cook, 1979; Florin et al., 1980).