Registration Dossier
Registration Dossier
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EC number: 402-070-1 | CAS number: 88122-99-0 UVINUL T 150
- 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 specific toxicokinetic data are available, however it can be predicted that the substance will have low oral and dermal bioavailability. It is expected that the physiochemical parameters will limit the distribution and metabolism of the substance. The majority of orally ingested product is expected to be excreted unchanged in the faeces.
Key value for chemical safety assessment
- Bioaccumulation potential:
- no bioaccumulation potential
Additional information
Absorption
The physiochemical parameters, such as molecular weight, water solubility and log P would strongly suggest that majority of any dose would not be absorbed following either oral of dermal exposure. Furthermore, oral sub-chronic and acute testing has shown that there is no overt toxicity produced by dosing with the substance which could suggest that the substance is not well absorbed.
Distribution
As with absorption, physiochemical parameters, such as molecular weight, water solubility and log P would strongly suggest that the majority of any oral dose would not be distributed beyond the site of exposure. With regards to bioaccumulation, the weight of evidence would suggest the Uvasorb ET has a very low BCF potential (1 L/kg; as estimated by the CAESAR structure activity relationship program).
Metabolism
It is difficult to predict metabolism in the absence of empirical data, and any metabolite produced will be in very small quantities (due to the lack of absorption and distribution). As such it is recommended that no further studies be conducted to further investigate this.
Excretion
Excretion following oral administration is expected to be mainly faecal due to the predicted lack of absorption.
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