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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
in vitro gene mutation study in bacteria
Remarks:
Type of genotoxicity: gene mutation
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
not applicable
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
other: Not according to GLP nor to specific test guidelines. Only 1 bacterial strain is used.
Cross-referenceopen allclose all
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to other study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2009
Report date:
2009

Materials and methods

Principles of method if other than guideline:
Bacterial gene mutation assay was used to test the test material for reversion of his- auxotrophs of Salmonella Thyphimurium in the strains TA1535, TA1537, TA98 and TA100 and tryp of Escherichia Coli wp2 uvrA
GLP compliance:
not specified
Type of assay:
bacterial gene mutation assay

Test material

Constituent 1
Reference substance name:
Residues, zinc smelting
EC Number:
273-824-3
EC Name:
Residues, zinc smelting
Cas Number:
69029-83-0
Molecular formula:
Not available, UVCB substance.
IUPAC Name:
Residues, zinc melting, alloying and casting
Details on test material:
name of test substance: Cenizas de cinc de segunda fusion
origin of test substance: Befesa Zinc Amorebieta

Method

Target gene:
not applicable
Species / strain
Species / strain / cell type:
E. coli WP2 uvr A
Details on mammalian cell type (if applicable):
not applicable
Additional strain / cell type characteristics:
not specified
Metabolic activation:
with and without
Metabolic activation system:
not specified
Test concentrations with justification for top dose:
312; 625; 1250; 2500 and 5000 µg/plate
Vehicle / solvent:
phosphate buffer
Controls
Untreated negative controls:
yes
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Remarks:
benzoapyrene
Positive control substance:
no
Remarks:
none
Details on test system and experimental conditions:
plate method: plate incorporation
endpoint: gene mutation
Evaluation criteria:
no information
Statistics:
no statistics reported

Results and discussion

Test results
Species / strain:
E. coli WP2 uvr A
Metabolic activation:
with and without
Genotoxicity:
negative
Remarks:
in vitro gene mutation
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Additional information on results:
none
Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'.

Any other information on results incl. tables

none

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative

This study reported that the test material was negative in Escherichia Coli with and without metabolic activation tested from 312-5000 µg/plate
Executive summary:

This study report demonstrated no mutagenic effect for the sample 'Cenizas de cinc de segunda fusion'