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EC number: 272-195-2 | CAS number: 68783-37-9 This substance is identified by SDA Substance Name: C16-C18 alkyl carboxylic acid lithium salt and SDA Reporting Number: 19-006-02.
- 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
Dissociation constant
Administrative data
Link to relevant study record(s)
Description of key information
The dissociation constants of the substances in the lithium salts of monocarboxylic acids category have been read across from the respective acids (measured as potassium or sodium salts). The acids (as potassium salts (from Kanicky 2002) or sodium salts (Kanicky 2000)) have measured pKA values of 8.1-8.2 (C14, sodium salt), 8.6-8.6 (C16, sodium salt), 9.24 (C18”, potassium salt), 9.85 (C18’, potassium salt) and 10.15 (C18, potassium salt). These values are relatively high, therefore these carboxylate substances are expected to be in the salt (ionic) form at environmental pH.
Key value for chemical safety assessment
Additional information
The substances are all lithium salts of monocarboxylic acids. Aqueous solutions of the substances are therefore expected to dissociate to free metal ions and carboxylic acid ions. The carboxylic acid ions would then be expected to achieve acid-base equilibrium, depending on the pKA of the carboxylic acid, at the pH of the solution. The dissociation constant of the substance is effectively represented by the dissociation constant(s) of the relevant carboxylic acid, as the ionisable moiety. As the monocarboxylic acids and the lithium salts of monocarboxylic acids are not soluble in water, data have been read across from the acids tested as potassium or sodium salts, which have higher solubility.
Reliable measured data available in the published literature for the dissociation constants of sodium and potassium salts of the relevant monocarboxylic acids have been used to complete this endpoint (Kanicky 2000, 2002): sodium myristate (C14), sodium palmitate (C16), potassium linoleate (C18”), potassium oleate (C18’) and potassium stearate (C18). The substances have measured pKA values of 8.1-8.2 (C14), 8.6-8.6 (C16), 9.24 (C18”), 9.85 (C18’’) and 10.15 (C18). These values are relatively high, therefore these carboxylate substances are expected to be in the salt (ionic) form at environmental pH.
Further investigations on the dissociation constant of lithium 12 -hydroxystearate are currently ongoing.
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