Registration Dossier

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:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Well documented study according to international accepted guidelines and GLP compliant.
Cross-reference
Reason / purpose:
other: Related to Richter composition
Reference
Name:
4-chloro-4'-fluorobutyrophenone
Type of composition:
boundary composition of the substance
State / form:
liquid
Reference substance:
Composition 1

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2014
Report Date:
2014

Materials and methods

Test guideline
Qualifier:
according to
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Deviations:
no
GLP compliance:
yes (incl. certificate)
Type of assay:
bacterial reverse mutation assay

Test material

Reference
Name:
Unnamed
Type:
Constituent
Test material form:
other: liquid
Details on test material:
Test item: 4-chloro-4’-fluorobutyrophenoneCAS No.: 3874-54-2Batch No.: 2607Physical state: liquidColour: yellowish greenStorage: cool, dry place in a tightly closed container

Method

Target gene:
S. typhimurium TA98: hisD3052; TA100: hisG46; TA1535: hisG46; TA1537: hisC3076E. coli WP2 uvr A: trpE
Species / strainopen allclose all
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Species / strain / cell type:
E. coli WP2 uvr A
Metabolic activation:
with and without
Metabolic activation system:
S9 mix
Test concentrations with justification for top dose:
The following concentrations of the test item were prepared and used in the Initial and Confirmatory Mutation Tests:In Salmonella typhimurium strains:-without metabolic activation: -S9 Mix: 1581, 1000, 750, 500, 250, 158 and 50 μg/plate;-with metabolic activation: +S9 Mix: 5000, 1581, 500, 158, 50 and 15.8 μg/plate;In Escherichia coli WP2 uvrA:-with and without metabolic activation: ±S9 Mix: 5000, 1581, 500, 158, 50 and 15.8 μg/plate.
Vehicle / solvent:
Dimethyl sulfoxide (DMSO)Ultrapure water (UPW)
Controlsopen allclose all
Untreated negative controls:
yes
Negative solvent / vehicle controls:
yes
Remarks:
DMSO, UPW
Positive controls:
yes
Remarks:
without metabolic activation
Positive control substance:
other: 4-nitro-1,2-phenylene-diamine
Remarks:
Dose: 4 μg/plate; Vehicle: DMSO; Strain: Salmonella TA98
Positive controls:
yes
Remarks:
without metabolic activation
Positive control substance:
sodium azide
Remarks:
Dose: 2 μg/plate; Vehicle: UPW; Strain: Salmonella TA100 and TA1535
Positive controls:
yes
Remarks:
without metabolic activation
Positive control substance:
9-aminoacridine
Remarks:
Dose: 50 μg/plate; Vehicle: DMSO; Strain: Salmonella TA1537
Positive controls:
yes
Remarks:
without metabolic activation
Positive control substance:
methylmethanesulfonate
Remarks:
Dose: 2 μL/plate; Vehicle: UPW; Strain: E. coli WP2uvrA
Positive controls:
yes
Remarks:
with metabolic activation
Positive control substance:
other: 2-aminoanthracene
Remarks:
Dose: 2 μg/plate; Vehicle: DMSO; Strain: all of Salmonella strains
Positive controls:
yes
Remarks:
with metabolic activation
Positive control substance:
other: 2-aminoanthracene
Remarks:
Dose: 50 μg/plate; Vehicle: DMSO; Strain: E. coli strain
Details on test system and experimental conditions:
The study included a Preliminary Solubility Test, a Preliminary Range Finding Test (Informatory Toxicity Test) an Initial Mutation Test (Plate Incorporation Test) and a Confirmatory Mutation Test (Repeated Plate Incorporation Test).In the different experimental phases of the study the plate incorporation method was used.
Evaluation criteria:
The colony numbers on the control, positive control and the test plates were determined (counted manually), the mean values and appropriate standard deviations and mutation rates were calculated.A test item is considered mutagenic if:- a dose–related increase in the number of revertants occurs and/or;- a reproducible biologically relevant positive response for at least one of the dose groups occurs in at least one strain with or without metabolic activation.An increase is considered biologically relevant if:- in strain Salmonella typhimurium TA100 the number of reversions is at least twice as high as the reversion rate of the vehicle control;- in strain TA98, TA1535, TA1537 and Escherichia coli WP2 uvrA the number of reversions is at least three times higher than the reversion rate of the vehicle control.

Results and discussion

Test resultsopen allclose all
Species / strain:
S. typhimurium TA 98
Metabolic activation:
without
Genotoxicity:
positive
Remarks:
frameshifts and base pair substitutions
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
the lowest cytotoxic concentration: 1581 μg/plate
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Species / strain:
S. typhimurium TA 100
Metabolic activation:
without
Genotoxicity:
positive
Remarks:
frameshifts and base pair substitutions
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
the lowest cytotoxic concentration: 1581 μg/plate
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Species / strain:
S. typhimurium TA 98
Metabolic activation:
with
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
the lowest cytotoxic concentration: 5000 μg/plate
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Species / strain:
S. typhimurium TA 100
Metabolic activation:
with
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
the lowest cytotoxic concentration: 5000 μg/plate
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Species / strain:
S. typhimurium TA 1535
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
the lowest cytotoxic concentration: 1000 μg/plate (-S9 mix), 5000 μg/plate (+S9 mix)
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Species / strain:
S. typhimurium TA 1537
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
the lowest cytotoxic concentration: 1000 μg/plate (-S9 mix), 5000 μg/plate (+S9 mix)
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Species / strain:
E. coli WP2 uvr A
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
the lowest cytotoxic concentration: 5000 μg/plate (+/-S9 mix)
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'.

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):positive S. typhimurium TA98 and TA100 tester strains carrying frameshift and base pair substitution mutation (-S9 Mix).In conclusion, the test item 4-Chloro-4’-fluorobutyrophenone (CAS 3874-54-2) as a directly-acting compound has mutagenic activity on Salmonella typhimurium TA98 and TA100 tester strains carrying frame shift and base pair substitution mutation, without exogenous metabolic activation (-S9 Mix) under the test conditions used in this study.