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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Type of information:
experimental study
Adequacy of study:
key study
Study period:
Feb - August 2006
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2006
Report date:
2006

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Version / remarks:
1997
GLP compliance:
yes (incl. QA statement)
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
4-{[(2-methoxyphenyl)formamido]sulfonyl}benzoyl chloride
EC Number:
617-251-2
Cas Number:
816431-72-8
Molecular formula:
C15H12ClNO5S
IUPAC Name:
4-{[(2-methoxyphenyl)formamido]sulfonyl}benzoyl chloride
Test material form:
solid: bulk

Method

Species / strain
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98, TA 100 and TA 102
Metabolic activation:
with and without
Metabolic activation system:
S9 mix of Aroclor 1254 induced rats
Test concentrations with justification for top dose:
16, 50, 158, 500, 1581, 5000 µg/plate for bacteria strains TA 98, TA 100, TA 102, TA 1535 and TA 1537 (plate incorporation and preincubation method)
500, 1000, 2000, 3000, 4000 and 5000 µg/ tube for strain TA102 (preincubation method only)
Controls
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
other: sodium azide, nitrofurantoin, 4-nitro-1,2-phenylene diamine, mitomycin C, cumene hydroperoxide and 2-aminoanthracene

Results and discussion

Test resultsopen allclose all
Key result
Species / strain:
S. typhimurium TA 102
Metabolic activation:
with and without
Genotoxicity:
positive
Cytotoxicity / choice of top concentrations:
no cytotoxicity
Vehicle controls validity:
valid
Positive controls validity:
valid
Key result
Species / strain:
other: TA 98, TA 100, TA 1535, TA 1537
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
starting from 1581 µg
Vehicle controls validity:
valid
Positive controls validity:
valid

Applicant's summary and conclusion

Conclusions:
Weak positive findings in strain TA 102 with and without metabolic activation.
Executive summary:

The Salmonella/microsome test, employing doses of up to 5000 ug per plate, showed AE 0001789-Amidchlorid to produce bacteriotoxic effects, starting at 1581 ug per plate.
Evaluation of individual dose groups, with respect to relevant assessment parameters (dose effect, reproducibility) revealed biologically relevant variations from the respective negative controls for TA 102. These were regarded as mutagenic effects of AE 0001789-Amidchlorid. Since the observed effect was weak and only detectable in high doses, it may be assumed, that the effect may be due to a by-product and not to AE 0001789-Amidchlorid itself.
In spite of the low doses used, positive controls increased the mutant counts to well over those of the negative controls, and thus demonstrated the system's high sensitivity. Due to this sensitivity, indications of mutagenic effects of AE 0001789-Amidchlorid could be found at assessable doses of up to 5000 ug per plate in Salmonella typhimuriumTA102. Due to these results the tested batch of AE 0001789-Amidchlorid has to be regarded as mutagenic.