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Diss Factsheets
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EC number: 939-626-2 | CAS number: 1474044-67-1
- 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 studies are available however based on physicochemical data, toxicity data and theoretical assessment, the basic toxicokinetics of Fatty acids C18 unsat, reaction products with pentaethylenehexamine, acetate salts can be adequately characterised. No absorption of the intact substance via the oral, dermal or inhalation routes is predicted. Consideration of distribution, metabolism and excretion is not therefore relevant. In the absence of systemic bioavailability, bioaccumulation is not predicted.
Key value for chemical safety assessment
- Bioaccumulation potential:
- no bioaccumulation potential
Additional information
No specific studies are required. According to Column 1 of Annex VIII of the REACH regulation, assessment of the toxicokinetic behaviour of the substance (to the extent that can be derived from the relevant available information) is required and this is provided. An adequate assessment of the basic toxicokinetics of the substance can be made from the existing toxicity data and theoretical considerations, without the need for specific testing.
Absorption
Oral absorption of the substance is not predicted according to Lipinski’s Rule (OECD QSAR Toolbox v3.1: OASIS); this is likely to be due to the high molecular weight of the substance. Toxicity data on the substance are limited to a study of acute oral toxicity; this study reported mortality in one group administered 2000 mg/kg bw and non-specific signs of toxicity at 300 mg/kg bw.
While oral absorption of the intact substance is not predicted, it is possible that hydrolysis of the substance in the gastrointestinal tract may result in the liberation of low molecular weight hydrolysis products which may be bioavailable and which may be able to exert toxicity. However the substance is predicted to be hydrolytically stable (including at gastrointestinal tract pH), therefore this is considered to be unlikely.
No data on dermal absorption are available; however based on the predicted absence of oral absorption, dermal absorption is similarly not predicted.
No data on inhalation absorption are available; however absorption is dependent on inhalation exposure which is not predicted based on the physicochemical properties (i.e. low vapour pressure and high boiling point) and the use pattern of the substance.
Oral absorption of the substance is not predicted. Nevertheless, for the purposes of risk assessment, the level of oral and dermal absorption are considered to be equivalent (default, worst-case assumption) and the extent of inhalation absorption is considered to be twice that of oral absorption (default assumption).
Distribution
Absorption of the intact substance or hydrolysis products is not predicted; therefore consideration of distribution is not relevant.
Metabolism
Absorption of the intact substance or hydrolysis products is not predicted; therefore consideration of metabolism is not directly relevant. However the OECD QSAR Toolbox predicts metabolism (by rat liver S9 fraction) through hydrolysis at the terminal amine group (with the liberation of acetic acid), at the central amide group or at the non-terminal secondary amine groups. The differential response of bacterial strains to the substance in the presence and absence of metabolic activation indicates a reduction of toxicity by metabolic enzymes.
Excretion
Absorption of the intact substance or hydrolysis products is not predicted; therefore consideration of excretion is not relevant.
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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