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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: GLP-Guideline study, however only 4 strains tested

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1988
Report date:
1988

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Deviations:
yes
Remarks:
4 strains only
GLP compliance:
yes
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
Methyl chloroformate
EC Number:
201-187-3
EC Name:
Methyl chloroformate
Cas Number:
79-22-1
Molecular formula:
C2H3ClO2
IUPAC Name:
methyl chloroformate
Details on test material:
- Name of test material (as cited in study report): chloroformic acid methyl ester
- Physical state: colorless liquid
- Analytical purity: 99.2 %
- Lot/batch No.: 2/i v Mai 87
- Storage condition of test material: 4°C

Method

Target gene:
his +/-
Species / strain
Species / strain / cell type:
other: Salmonella typhimurium TA 98, 100, 1535, 1537
Metabolic activation:
with and without
Metabolic activation system:
S9 -mix
Test concentrations with justification for top dose:
0.0005 µl - 5.0 µl/Platte (TA 1535); 0.0005 - 1.0 µl/Platte (TA 100, 1537, 98), respectively 0.5-5000 µg/Platte (TA 1535); 0.5 - 1000µg/Platte (TA 100, 1537, 98)
Vehicle / solvent:
- Vehicle(s)/solvent(s) used: ethanol
- Justification for choice of solvent/vehicle: stability and soloubility
Controlsopen allclose all
Untreated negative controls:
yes
Negative solvent / vehicle controls:
yes
Positive controls:
yes
Positive control substance:
other: 2- amino anthracene
Remarks:
all strains with s9 mix
Untreated negative controls:
yes
Negative solvent / vehicle controls:
yes
Positive controls:
yes
Positive control substance:
other: TA 100; TA 1535: N-methyl-N'-nitro-N-nitrosoguanidine; TA 98 : 4-nitro-o-phenylendiamine; TA 1357 : 9-aminoacridine
Remarks:
with out S-9 mix
Details on test system and experimental conditions:
METHOD OF APPLICATION: in agar (plate incorporation); preincubation

DURATION
- Preincubation period: 20 min
- Exposure duration: 48-72 h

DETERMINATION OF CYTOTOXICITY
- Method: relative total growth
Evaluation criteria:
The test chemical is considered positive in this assay if the following criteria are met:

In general, the test is considered as positive if the following requirements are fulfilled:
 
Doubling of the spontaneous mutation rate (control)
Dose response relationship
Reproducibility of the results
Statistics:
mean + sd

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:
cytotoxicity
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'.

Any other information on results incl. tables

Raw data see attached file.

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative