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EC number: 420-380-5 | CAS number: 136465-81-1
- 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
Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
Ro 31 -9373/000 was tested in four strains of S. typhimurium (TA97, TA98, TA100 and TA102) in a standard plate incorporation and pre-inubation modification of the Ames test for mutagenic activity. The test material was disolved in DMSO and administered at concentrations ranging from 50 to 5000 ug/plate, in the presence or absence of metabolic activation in the form of rat liver induced S-9. Ro 31 -9373/000 was not toxic up to the maximal concentration tested in the standard plate incorporation assay but signs of toxicity were evident in the pre-incubation assay at 1666 ug/ml.
No increase in the his+ revertants was evident, PTH-decahydroamide was not found to be mutagenic under the conditions of this assay.
In a replicated assay to determine the effects of PTH-decahydroamide on the induction of chromosomal aberrations in cultured peripheral human lymphocytes, cultures were prepared with or without metabolic activation (rat liver S-9 mix) and tested using concentrations of up to 1000 ug/ml for 24 or 48 hour fixation periods. None of the concentrations evaluated gave a postive response under the test conditions. Vehicle and positive control cultures gave responses consistent with historical ranges and met the acceptance criteria for the assay. PTH-decahydroamide was not clastogenic under the conditions of this assay.
Short description of key information:
Negative responses are seen in an Ames test and a study of clastogencity in human pepripheral lymphocytes in vitro. Studies were performed in the presence and absence of metabolic activation.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
Both in vitro studies - a clastogenicity investigation with human cultured peripheral lymphocytes and an Ames test using four strains of S.typhimurium - gave negative responses for mutagenicity. No classification is warranted for PTH-decahydroamide based on the available data.
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