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Diss Factsheets
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EC number: - | CAS number: -
- 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
Genetic toxicity in vitro
Description of key information
The in vitro genetic toxicity assessment of SPE1415 is based on a combination of data on the substance itself and read-across data from the structural analogues ATMP (acid/sodium salt) and DTPMP (acid/sodium salt). Additional supporting data on another confidential analogue substance is discussed in Additional Information.
There are a total of ten in vitro genetic toxicity studies presented. This includes four in vitro bacterial mutation studies, three in vitro mammalian cell gene mutation studies and three in vitro cytogenetics studies. One in vitro bacterial mutation study was conducted on the substance itself and the other nine studies were all conducted on the structural analogues. All of the studies were reliable and all except one gave negative results.
The in vitro cytogenetics assay on DTPMP sodium salt was the only study which gave a positive result however this finding was not supported by the negative result from the in vivo cytogenetics assay on DTPMP acid. It is probable that the positive response for DTPMP sodium salt does not reflect an ability to interact with DNA due to (1) lack of structural alerts for mutagenicity, (2) lack of evidence for gene mutation potential in sub-mammalian systems and (3) lack of potential to induce gene mutations in another well-conducted assay investigating mutations at the hprt locus in CHO cells. It is also inconsistent with the gentoxicity findings from the various studies on ATMP and SPE1415 itself.
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Genetic toxicity in vivo
Description of key information
The in vivo genetic toxicity assessment of SPE1415 is based on read-across data from the structural analogues ATMP (sodium salt) and DTPMP (acid). Additional supporting data on another confidential analogue substance is discussed in Additional Information.
There are a total of three in vivo genetic toxicity studies presented. This includes an in vivo micronucleus study on ATMP (sodium salt), and in vivo cytogenetics study on DTPMP (acid) and in vivo micronucleus assay on another analogue substance. All of the studies were reliable and all gave negative results.
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Additional information
Justification for classification or non-classification
The substance and its structural analogues overwhelmingly give negative results in a variety of reliable in vitro and in vivo gentoxicity assays. Therefore there is no justification for classification of the substance.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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