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EC number: 618-777-5 | CAS number: 91662-51-0
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data

Genetic toxicity: in vitro
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:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: study performed according to OECD and GLP guidelines
Cross-reference
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 997
- Report date:
- 1997
Materials and methods
Test guideline
- 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
Test material
- Reference substance name:
- Zeanyne salt
- EC Number:
- 618-777-5
- Cas Number:
- 91662-51-0
- Molecular formula:
- C33H36ClOP
- IUPAC Name:
- Zeanyne salt
Constituent 1
Method
- Target gene:
- TA97: hisD6610, TA 98: hisD3052; TA 100 hisG46 TA102 hisG428 and TA 1535 hisG46
Species / strain
- Species / strain / cell type:
- other: TA97, TA 98, TA 100, TA102 and TA 1535
- Additional strain / cell type characteristics:
- other: rfa, delta-uvrB, pKM101, pAQ1
- Metabolic activation:
- with and without
- Metabolic activation system:
- S9
- Test concentrations with justification for top dose:
- 0, 1, 3, 10, 33, 100, 333, 1000, 3333, 5000 ug/plate in the preliminary test,
2 to 200 ug/plate in the main experiment
Controls
- Untreated negative controls:
- yes
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- 2-nitrofluorene
- sodium azide
- mitomycin C
- other: ICR 191, 2-Aminoanthracene
Results and discussion
Test results
- Species / strain:
- other: TA97, TA 98, TA 100, TA102 and TA 1535
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not determined
- 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
-
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information):
negative
Neither Zeanyne salt per se, nor any of the formed metabolites was mutagenic in the Ames test under the described experimental
conditions. - Executive summary:
Zeanyne salt was evaluated for mutagenic activity in the Ames test. A standard plate incorporation and a
preincubation modification assay in absence and in presence of an exogenous
metabolic activation system (S9) were performed. Five Salmonella typhimurium tester strains (TA1535, TA97, TA98, TA100, and TA102) were employed. The activity of the S9-mix and the responsiveness of the tester strains were verified by including
appropriate controls into each experiment.
The substance was dissolved in dimethylsulfoxide (DMSO). Toxic effects were observed in a preliminary toxicity experiment starting at 333 ug/plate (on VB plates).
Therefore the concentration range 2 to 200 pg/plate was evaluated in the main experiments. Upon addition to the aqueous medium no precipitation of the compound was observable. Strain dependent toxic effects were observed (reduction in the number
of revertants and/or reduction in the background growth). Using the preincubation
modification assay, known to be more sensitive for several class of compounds, the
toxic effects were more pronounced. No increase of the number of mutant colonies was apparent in any of the five investigated
tester strains. Thus it can be concluded, that neither Zeanyne salt per se, nor any of the formed
metabolites was mutagenic in the Ames test under the described experimental conditions.
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