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Diss Factsheets
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EC number: 701-269-3 | 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
Link to relevant study record(s)
Description of key information
No experimental toxicokinetic studies are available on the substance. However, as per REACH guidance document R7. C (May 2008), information on absorption, distribution, metabolism and excretion may be deduced from the physicochemical properties. Based on the toxicological data and the physicochemical properties, a very low absorption of the substance is expected by oral and dermal route while the physical form of the substance will favour the deposition on the surface of the lower respiratory tract.
Key value for chemical safety assessment
Additional information
No experimental toxicokinetic study is available on the substance but information on absorption, distribution, metabolism and excretion may be deduced from the following physicochemical properties:
- Molecular weight: the molecular weight is around 625 g/mol,
- Water solubility: the water solubility measured at 25°C according to OECD Guideline 105 is < 0.115 mg/L,
- Partition coefficient: based on the read-across substance bisamide (UVCB), the log Kow measured according to OECD Guideline 117 is ≥ 5.86 while the calculated values gave a range of estimations between 11.3 and 18.64 for the three main constituents,
- Particle size: The proportion of test substance having a particle size below 100 µm was found to be < 0.266%.
Absorption
The log Kow, the extremely low water solubility, the molecular weight and the solid form suggest a very low absorption from the gastro-intestinal (GI) tract after oral absorption. Indeed the absorption of highly lipophilic substances may be limited by the inability of such substances to dissolve into GI fluids. The 'particle' form limits also the absorption because of the time taken for particle to dissolve, especially for poorly water-soluble substances.
This assumption of a very low oral absorption is confirmed in the oral toxicity studies: no systemic effects or mortalities were observed in rats treated with the read-across substance bisamide (UVCB) at 2,000 mg/kg bw in an acute toxicity study and at 1,000 mg/kg bw/day in a 14 day repeated dose toxicity study.
With extremely low water solubility, a high value of log Kow and a molecular mass above 500 g/mol, dermal absorption is also anticipated to be low although the substance exhibits a sensitizing potential.
Regarding the inhalation route, the size of the particles will favour deposition on the surface of the lower respiratory tract. As the particles are poorly water-soluble, those deposited in the alveolar region will mainly be engulfed by macrophages. The macrophages may either translocate particles to the ciliated airways for elimination or carry particles into the pulmonaryintersticium. Thus, absorption should be very limited. This assumption is confirmed in the inhalation toxicity studies: no systemic effects or mortalities were observed in rats exposed 4 h to 5.05 mg/L air in an acute toxicity study with the read-across substance bisamide (UVCB), and up to 2.02 mg/L air six hours per day, five days per week in a 14 day repeated dose toxicity study.
Distribution and metabolism
'By the dermal route, as the substance is highly lipophilic, it may persist in the lipid richstratum corneumand will eventually be cleared as this layer is sloughed off. By the inhalation route, as the particles of the substance are poorly water-soluble, they may stay in the pulmonaryintersticium, where they will be engulfed by macrophages, degrade and removed by mucus secretions.
No specific data is available on the metabolism of the substance.
Elimination
Due to the extremely low water solubility and a relatively high molecular mass, excretion of the substance in urine is not expected. An excretion via bile and faeces is possible.
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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