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Diss Factsheets
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EC number: 203-677-2 | CAS number: 109-52-4
- 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
Additional information
Three fish studies were available for Valeric Acid. Two studies were non-GLP with fish exposed to pure Valeric Acid, while the third GLP study exposed Rainbow Trout to a commercial mixture of ca. 64% Valeric Acid and 36% 2 -methylburtyric acid. Reportable endpoints included a 96 -hr LC50 value of 39 mg/L with Pimephales promelas exposed to pure Valeric Acid and a higher value of 75.9 mg/L for Rainbow Trout exposed to the mixture. In a preliminary study with the mixture in which the pH of the test solutions were adjusted to approximately that of control water, no fish mortality occurred up through the highest concentration of 1000 mg/L. A short-term NOEC of 500 mg/L was reported for the golden orfe.
Two studies are available to assess the acute toxicity of Valeric Acid to the cladoceran, Daphnia magna. A GLP-guideline study conducted with a commercial mixture of valeric acid (ca. 64%) and 2 -methylbutyric acid (ca. 36%) has been selected as the key study as this study is reliable without restrictions (Klimisch 1). The EC50 (48 hours) reported in this study is 88.1 mg/l and was determined from test solutions with no pH adjustment. A preliminary study with the mixture showed that toxicity was reduced with no mortality of test organisms occurring through 100 mg/L with pH adjustment of the test solutions. This endpoint is supported by a non-GLP study conducted with pure valeric acid. The EC50 (48 hours) reported in this supporting study is 45 mg/l.
Two studies are available to assess the acute toxicity of valeric acid to algae. A GLP-guideline study conducted with pure valeric acid
has been selected as the key study as this study is reliable without restrictions (Klimisch 1). The ErC50 (72 hours) reported in this study is 29.3 mg/l. This endpoint is supported by a GLP-study conducted with a commercial mixture of valeric acid (ca. 64%) and 2 -methylbutyric acid (ca. 36%). The ErC50 (48 hours) reported in this supporting study is 73.2 mg/l.
A toxicity to microorganisms study with limited documentation reported that no toxicity was observed at 1500 mg/L Valeric Acid.
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