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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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:
comparable to guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1986
Report date:
1981

Materials and methods

Test guideline
Qualifier:
no guideline available
Guideline:
other: Ames test but no guideline named
GLP compliance:
yes (incl. QA statement)
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Reference substance name:
Benzoylchloride, 2,4-dichloro-
IUPAC Name:
Benzoylchloride, 2,4-dichloro-
Constituent 2
Chemical structure
Reference substance name:
2,4-dichlorobenzoyl chloride
EC Number:
201-936-4
EC Name:
2,4-dichlorobenzoyl chloride
Cas Number:
89-75-8
Molecular formula:
C7H3Cl3O
IUPAC Name:
2,4-dichlorobenzoyl chloride
Test material form:
other: clear liquid
Details on test material:
2,4-Dichlorobenzoyl chloride: purity: at least 99 %, Storage conditions: dark 22°C
At the day of the experiment the substance was dissolved in DMSO at the appropriate concentration.

Method

Target gene:
In the Salmonella typhimurium strains (TA 1535, TA 100, TA 1537, TA 1538, TA 98) the amino acid histidine locus is the target gene.
In the Escherichia coli strain (WP2 uvrA) the amino acid tryptophan locus is the target gene.
Species / strain
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98, TA 100 and E. coli WP2
Remarks:
additionan S. typhimurium TA 1538
Metabolic activation:
with and without
Metabolic activation system:
rat liver homogenate fraction( " S-9")
Test concentrations with justification for top dose:
The dose range of 6 different doses from 4 µg/plate to 10 000 µg/plate and from 0.8 µg/plate to 25000 µg/plate was used. Find attached the exact concentrations plus result in the attached background material.
Vehicle / solvent:
DMSO
Controls
Untreated negative controls:
yes
Negative solvent / vehicle controls:
yes
Remarks:
DMSO
Positive controls:
yes
Positive control substance:
9-aminoacridine
2-nitrofluorene
N-ethyl-N-nitro-N-nitrosoguanidine
benzo(a)pyrene
other: 2-Aminoanthracene
Details on test system and experimental conditions:
Mutagenicity Test: Top agar is prepared for Salmonella strain . Bacteria are grown overnight in nutrient broth.The suitable amount of bacteria in cell suspension is checked by nephelmetry. For inoculation, stock cultures which are stored at -80 °C are used.

Results and discussion

Test resultsopen allclose all
Species / strain:
S. typhimurium, other: TA 100, TA 1535, TA 1537, TA 1538, TA98
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Species / strain:
E. coli WP2 uvr A
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Additional information on results:
Sterility of S-9 Mix and the test compound was indicated by the absence of contamination on the test material and S-9 Mix sterility check plates. Control plates (background control and positive controls) gave expected number of colonies.

Applicant's summary and conclusion

Conclusions:
Summarizing, it can be stated that 2,4-Dichlorbenzoyl chloride is not mutagenic in these bacterial test system either with or without exogenous metabolic activiation at the dose level investigated.
Executive summary:

2,4-Dichlorobenzoyl chloride was tested for mutagenicity with strains TA 100, TA 1535, TA 1537, TA 1538, TA 98 of Salmonella typhimurium and Escherichia coli WP2uvrA.

Mutagenicity: In the absence of metabolic activation system the test compound did not show a dose dependent increase in number of revertants in any of the bacterial strains. Also in the presence of a metabolic activivation system, treatment of the cells with 2,4 -Dichlorobenzoyl chloride did not result in relevant increases in number of revertant colonies. It can be concluded that the substance is not mutagenic.