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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Genetic toxicity in vitro

Link to relevant study records
Reference
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:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
GLP compliance:
yes (incl. QA statement)
Type of assay:
bacterial reverse mutation assay
Species / strain / cell type:
S. typhimurium TA 100
Metabolic activation:
with and without
Positive controls:
yes
Remarks:
The following mutagenic substances were used as positive controls: 6.2.1 4-Nitro1,2-phenylene diamine 4-Nitro-1,2-phenylene diamine, C6H7N3〇2; CAS-No.: 99-56-9
Details on test system and experimental conditions:
General Preparation: Per strain and dose, four plates with and four plates without S9 mix were used. The test item solutions were prepared and membrane filtered in order to accomplish sterility.
Top agar basis was melted in a microwave oven, after melting 10 mL of histidine-biotin-solution 0.5mMol per 100 mL basis was added and the bottle was placed in the water bath at 43°C.

Plate incorporation method: the following materials were slightly vortexed in a test tube and poured onto the selective agar plates:
• 100 µL test suspension at each dose level, solvent (negative control) or reference mutagen solution (positive control)
• 500 µL S9 mix or phosphate buffer
• 100 µL bacteria suspension
• 2200 µL overlay agar
The plates were closed and left to harden for a few minutes, then inverted and placed in the dark incubator at 37°C.

Pre incubation method: The following materials were gently vortexed in a test tube and incubated at 37°C for 20 minutes:
• 100 µL test suspension at each dose level, solvent (negative control) or reference mutagen solution (positive control)
• 500 µL S9 mix or phosphate buffer
• 100 µL bacteria suspension
After pre-incubation 2000µL overlay agar (top agar) was added, the tube was gently vortexed and the mixture was poured onto the selective agar plate.
Species / strain:
S. typhimurium TA 100
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity

The test item Casamid 710 is considered as "not mutagenic under the conditions of the test".

Conclusions:
Interpretation of results (migrated information):
negative with metabolic activation

The test item Casamid 710 is considered as "not mutagenic under the conditions of the test".
Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (negative)

Additional information

Justification for classification or non-classification