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Diss Factsheets
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EC number: 413-110-2 | CAS number: 135861-56-2
- 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
Based on measurements made for physical chemistry properties and qualitative observations for systemic toxicology, the test substance is considered to have only a low potential for absorption and bioaccumulation.
Key value for chemical safety assessment
- Bioaccumulation potential:
- low bioaccumulation potential
Additional information
The low water solubility of the substance (0.0476 mg/l), its relatively high molecular weight (414.49) and moderate water/octanol partition coefficient (Log Kow 2.78-3.5) indicates that, on balance, the test substance has a potential for low bioavailability.
The low potential for absorption via the gastro-intestinal tract is supported by the mild systemic effects apparent at high dosages in sub-acute and sub-chronic oral toxicity studies in rats.(Section 5.6.3) and the complete absence of effects following acute oral exposure (Section 5.2.3). A limited uptake via the lymphatic system cannot be excluded.
The test substance is a dimethyl benzylidene derivative of sorbitol, .The four ether bonds would be expected to be relatively stable, so the primary metabolic pathway would probably be via the oxidation of the sorbitol carbon chain to give diols, dicarboxylic acids or a combination of the two. . The residual benzylidine moiety, alcohols and carboxylic acids could be conjugated with glucuronic acid to give hydrophilic metabolites that would be readily excreted. None of the metabolites formed by these processes would be considered to have any genotoxic potential.
There is no toxicological evidence of distribution to the central nervous system, but the moderate water/octanol partition coefficient would indicate slight potential for tissue accumulation.
The absence of systemic effects following acute dermal exposure to the test material (Section 5.2.3) indicates that no significant absorption occurs through the skin, and the very low vapour pressure and modest particle size (median diameter 14µm) suggests that the air concentration of the substance available for absorption via the lungs would be low.
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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