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EC number: 425-220-8 | CAS number: 5945-33-5
- 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
Gene Mutation in vitro
Bacteria
The substance (1-methylethylidene)di-4,1-phenylenetetraphenyl diphosphate (CAS No. 5945-33-5) was tested in three in vitro gene mutation study in bacteria (Reverse Mutation Assay, Ames Test). Two guideline assays tested up to 5000ug/plate however precipitation was noted at 100ug/plate and 1000ug/plate. The assay chosen as the key study was performed in accordance with GLP and according to OECD 471 guidelines. Precipitation of the substance was noted at 500ug/plate. None of the strains tested (S. typhimurium TA 1535, TA 1537, TA 98, TA 100 and E. coli WP2uvrA) showed evidence of mutagenic activity, either in the absence or in presence of S9 mix.
Mammalian cells in vitro
Chromosome aberration
The substance (1-methylethylidene)di-4,1-phenylenetetraphenyl diphosphate (CAS No.5945-33-5) was tested in three in vitro chromosome abberration assays in mammalian cells (in vitro mamamalian cytogenicity assay). In the key study was tested in human lymphocytes with and without S9. There were no significant increases in structural chromosomeal aberrations were seen following 21 hour non-activated treatments or 3 hour treatments with S-9. The substance did not display clastogenic activity in this assay.
Gene mutation in vitro mammalian cell
Gene mutation
The substance 1-methylethylidene)di-4,1-phenylenetetraphenyl diphosphate (CAS No. 5945-33-5) was tested in one in vitro gene mutation study in mammalian cells. In this assay (OECD 476/GLP), mouse lymphoma L5178Y cells cultured in vitro were exposed to the test substance in DMSO at concentrations of 5.0 to 200 µg/mL in the presence and absence of mammalian metabolic activation (Aroclor-induced rat liver S9). There was no concentration-related increase in mutant frequency. The colony sizing for the MMS and DMBA positive controls yielded the expected increase in small colonies and large colonies. Under the conditions of this study, the substance was concluded to be negative.
Short description of key information:
In vitro:
Gene Mutation (Bacterial Reverse Mutation Assay/Ames test): (1-methylethylidene)di-4,1-phenylenetetraphenyl diphosphate (CAS No. 5945-33-5) did not show mutagenic activity using S. typhimurium TA 1535, TA 1537, TA 98, TA 100 and and E. coli WP2uvrA in the presence or absence of metabolic activation (OECD 471/GLP).
Chromosome aberration (Mammalian in vitro cytogenicity): (1-methylethylidene)di-4,1-phenylenetetraphenyl diphosphate (CAS No. 5945-33-5) did not display clastogenic activity in this assay (Annex V; GLP).
Gene mutation (in vitro mammalian cell gene mutation test): the substance 1-methylethylidene)di-4,1-phenylenetetraphenyl diphosphate (CAS No. 5945-33-5) does not induce gene mutations in mouse lymphoma L5178Y cells in the presence or absence of S9 metabolic activation (OECD 476, GLP);
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
Based on the available information in the dossier, the substance (1-methylethylidene)di-4,1-phenylenetetraphenyl diphosphate (CAS No. 5945-33-5) does not need to be classified for genetic toxicity when the criteria outlined in Annex I of 1272/2008/EC is applied.
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