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Diss Factsheets
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EC number: 700-802-7 | 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
Additional physico-chemical information
Administrative data
Link to relevant study record(s)
Description of key information
As indicated before, the addition of acetate groups to the polyamines increase their water solubility. The polyamines when dissolved in water take up positive charged hydrogens to become cationic substances. As a consequence the water solution becomes alkaline. With the addition of acetic acid, the cationic substance is already present in the Polyamine acetates, linked to the negatively charged acetate ions. The polyamine acetate substance is therefore more easily soluble in water, which can only be explained from the dissociation of the acetate ions, as without that, uncharged molecules would not be easier soluble. Following the dissociation of the polyamine acetate salts, there is no principle difference after absorption of the polyamine structures following exposure as polyamines as such or as polyamine acetate.
Additional information
As indicated before, the addition of acetate groups to the polyamines increase their water solubility. The polyamines when dissolved in water take up positive charged hydrogens to become cationic substances. As a consequence the water solution becomes alkaline. With the addition of acetic acid, the cationic substance is already present in the Polyamine acetates, linked to the negatively charged acetate ions. The polyamine acetate substance is therefore more easily soluble in water, which can only be explained from the dissociation of the acetate ions, as without that, uncharged molecules would not be easier soluble. Following the dissociation of the polyamine acetate salts, there is no principle difference after absorption of the polyamine structures following exposure as polyamines as such or as polyamine acetate.
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