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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
genetic toxicity in vitro
Remarks:
Type of genotoxicity: genome mutation
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
Not reported
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
documentation insufficient for assessment

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1984

Materials and methods

Principles of method if other than guideline:
The test material was studied to determine the ability to cause DNA damage and thereby induce a pleiotropic response in the E. coli strain. The pleiotopic response was determined by checking for the induction of λ prophage.
GLP compliance:
not specified
Type of assay:
other: Induction of λ prophage in E. coli WP2s (λ)

Test material

Constituent 1
Reference substance name:
Zinc chloride
EC Number:
231-592-0
EC Name:
Zinc chloride
Cas Number:
7646-85-7
IUPAC Name:
zinc dichloride
Details on test material:
- Name of test material (as cited in study report): Zinc chloride

Method

Target gene:
Not reported
Species / strain
Species / strain / cell type:
E. coli WP2
Details on mammalian cell type (if applicable):
- Type and identity of media: Minimal Broth Davis (Difco) containing 0.2 % glucose and 20 µg/mL tryptophan (MST)
Additional strain / cell type characteristics:
not specified
Metabolic activation:
not specified
Metabolic activation system:
Not reported
Test concentrations with justification for top dose:
3.2 mM
Vehicle / solvent:
- Vehicle(s)/solvent(s) used: Minimal Broth Davis (Difco) containing 0.2 % glucose and 20 µg/mL tryptophan (MST)
Controlsopen allclose all
Untreated negative controls:
yes
Remarks:
Streptomycin
Negative solvent / vehicle controls:
yes
Remarks:
Minimal Broth Davis (Difco) containing 0.2 % glucose and 20 µg/mL tryptophan (MST)
True negative controls:
no
Positive controls:
yes
Positive control substance:
other: N-Methyl-N'-nitro-N-nitrosoguanidine
Untreated negative controls:
yes
Remarks:
Streptomycin
Negative solvent / vehicle controls:
yes
Remarks:
Minimal Broth Davis (Difco) containing 0.2 % glucose and 20 µg/mL tryptophan (MST)
True negative controls:
no
Positive controls:
yes
Positive control substance:
4-nitroquinoline-N-oxide
Details on test system and experimental conditions:
METHOD OF APPLICATION: in medium


DURATION
- Exposure duration: 20 h


NUMBER OF REPLICATIONS: Duplicate


Evaluation criteria:
Clear (non-turbid) wells can occur because of toxicity of the test agent, inhibition of growth, or induction of λ prophage and cell lysis. Thus clear wells indicate toxicity and growth inhibition.
Statistics:
Not reported

Results and discussion

Test results
Species / strain:
E. coli WP2
Metabolic activation:
without
Genotoxicity:
ambiguous
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Additional information on results:
Not reported

Any other information on results incl. tables

None

Applicant's summary and conclusion

Conclusions:
Under the test conditions, 3.2 mM of the test material caused two-fold increase in induction of λ prophage over control (reported as +/-).
Executive summary:

A study was conducted to determine the potential of the test material for induction of λ prophage in E coli WP2 (λ).

 

The test material in MST was inoculated with 75 µL of a mid-exponential culture of WPs(λ) diluted so that each well receives approximately 2 x 107bacteria. The test plate was incubated at 37 °C and scored after 20 h for turbidity. MNNG and 4NQO served as positive controls and streptomycin as negative control.

 

Under the test conditions, 3.2 mM of the test material caused a two-fold increase in induction of λ prophage over control (reported as +/-).