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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
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:
After dissolution and disociation in environmental (aqueous)/physiolological media the constituents of tin difluoride become bioavailable and the overall toxicity of the dissociated substance can be described by the toxicity of the individual constituents/ions. Since synergistic effects are not to be expected, the human health and environmental hazard assessment of the assessment entity tin difluoride consists of an individual assessment of the assessment entities tin cation and the fluoride anion. The tin cation and the fluoride anion are considered to represent the overall toxicity of tin difluoride in a manner proportionate to the fluoride and the metal (represented by one of its readily soluble salts). Based on the above information, unrestricted read-across is considered feasible and justified.

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1990
Report date:
1990
Reference Type:
publication
Title:
Salmonella mutagenicity test results for 250 chemicals
Author:
Haworth, S. et al.
Year:
1983
Bibliographic source:
Environmental Mutagenesis, Supplement 1: 3 - 142.

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: Ames Salmonella/mammalian microsome test
GLP compliance:
not specified
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Reference substance name:
Sodium fluoride
EC Number:
231-667-8
EC Name:
Sodium fluoride
Cas Number:
7681-49-4
IUPAC Name:
sodium fluoride
Details on test material:
- Name of test material (as cited in study report): sodium fluoride
- Analytical purity: 99%
- Lot/batch No.: DC 030887

Method

Species / strain
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Metabolic activation:
with and without
Metabolic activation system:
Aroclor 1254-induced male Sprague-Dawley rat or Syrian hamster liver S9
Test concentrations with justification for top dose:
0, 100, 333, 1000, 3333 and 10000 ug NaF/plate
Vehicle / solvent:
- Vehicle(s)/solvent(s) used: Dimethylsulfoxide
Controls
Untreated negative controls:
yes
Negative solvent / vehicle controls:
yes
Remarks:
dimethylsulfoxide (DMSO)
Positive controls:
yes
Positive control substance:
9-aminoacridine
sodium azide
other: 2-aminoanthracene and 4-nitro-o-phenylenediamine
Details on test system and experimental conditions:
METHOD OF APPLICATION: in agar (plate incorporation); refer to Haworth (1983) for details

DURATION
- Preincubation period: 20 minutes at 37 °C
- Exposure duration: 48 hours

NUMBER OF REPLICATIONS: Two


Evaluation criteria:
A positive response was defined as a reproducible, dose-related increase in histidine-independent (revertant) colonies in any one strain/activation combination. An equivocal response was defined as an increase in revertants that was not dose-related, not reproducible, or of insufficient magnitude to support a determination of mutagenicity. A negative response was obtained when no increase in revertant colonies was observed following chemical treatment.
Statistics:
Revertants were presented as mean ± the SD from 3 plates.

Results and discussion

Test results
Species / strain:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Additional information on results:
Sodium fluoride did not induce gene mutations in any of the strains of Salmonella typhimurium tested.
Definitive cytotoxicity was not observed in any Salmonella typhimurium strains at doses up to 10,000 ug/plate

Applicant's summary and conclusion

Conclusions:
Sodium fluoride did not induce gene mutations in Salmonella typhimurium strains TA100, TA1535, TA1537 and TA98 when tested with a preincubation protocol at doses of 100 to 10,000 ug/plate. All strians were tested with or without Aroclor 1254-induced male Sprague-Dawley or Syrian hamster liver S9.