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Diss Factsheets
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EC number: 200-522-0 | CAS number: 61-90-5
- 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
Description of key information
Key value for chemical safety assessment
Skin sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
No test results for L-leucine are available. However, read-across to the test results available for structural analogue L-valine is deemed justified based on a comparison of the main factors driving skin sensitisation: the chemical reactivity (functional groups) of the substance and its tendency to undergo dermal absorption, which in itself is determined by the substance's molecular weight, log Kow and water solubility.
- both are essential amino acids that are in the zwitterion state at physiological pH
- the chemical structure differs only in that L-leucine has one extra methylene group in the aliphatic side chain
- both amino acids are quite small molecules with a low MW (LEU: 131 g/mol, VAL: 117 g/mol), which favors dermal uptake, however
- both amino acids have log Kow values below -1 (LEU: -1.52, VAL: -2.26) which suggests that these substances are most likely not sufficiently lipophilic to cross the stratum corneum
- the water solubility of leucine and valine is high (LEU: 23 g/L, VAL: 58 g/L). In combination with a low log Kow, it can be assumed that these substances will be too hydrophilic to cross the lipid rich environment of the stratum corneum. As a consequence, dermal uptake will be low.
As the chemical reactivity and the dermal uptake of L-leucine and L-valine are almost identical, it can be concluded that read-across of skin sensitisation information between those 2 substances is acceptable.
The tests available for L-valine are carried out according to OECD guidelines and reveal no effects of skin sensitisation. L-valine was concluded to not be sensitising to the skin. As a consequence, skin sensitisation effects are not expected to occur upon exposure to L-leucine.
Migrated from Short description of key information:
No test results for L-leucine are available. However, based on test results available for read-across substance L-valine it can be concluded that skin sensitisation is not expected upon exposure to L-leucine.
Justification for classification or non-classification
In accordance to Directive 67/548/EEC (Dangerous Substances Directive), classification is not necessary for skin sensitisation based on the available test data for read-across substance L-valine.
In accordance to EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008, classification is not necessary for skin sensitisation based on the available test data for read-across substance L-valine.
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