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EC number: 203-341-5 | CAS number: 105-87-3
- 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
Additional information
Skin irritation
No key study is available for geranyl acetate. In a skin irritation test in rabbits not according to current guidelines, geranyl acetate was applied open to the clipped skin of 6 rabbits for 24 hours (Motoyoshi, 1979). 30 min after first reading, the skin was clipped again and a new application of geranyl acetate followed. Another reading was then done 48 h after the start of 2nd exposure. Intravenous injection of Evans Blue was made and 1 h after injection dorsal skin was removed to asses dilating rate and capillary permeability. Primary irritation index was determined as the total of the averages of reddening rate (erythema, 72 hours reading) + dilating rate (of blood vessels) + swelling rate (edema) + blueing rate (as a result of increased capillary permeability). Geranyl acetate was reported to be severely irritating (no further data given).
Further skin irritation data from a structurally and metabolically related substance, i.e. geraniol (CAS 106-24-1) give further indications for a the skin irritating potential of geranyl acetate. The skin irritation potential of geraniol was analyzed in a study with three experiments performed according to OECD guideline 404 as stated in the ECETOC Technical Report No. 66 (Givaudan, 1995). In these experiments, 0.5 ml of geraniol was applied to three to four rabbits for 4 h and the application site was observed the following 7 days. Resulting erythema and edema were scored 24, 48 and 72 h later, as well as 7 days after application and scored according to Draize. The results were erythema scores of 2, 2.08 and 1.92 and edema scores of 1.67, 1.25 and 1 in the experiments 1, 2 and 3, respectively. Since the irritation effects were still apparent and desquamation was noted at the end of observation time geraniol is regarded as irritating to skin.
Overall in a weight of evidence, geranyl acetate is considered to be irritating to skin.
Eye irritation
No key study for eye irritation is available for geranyl acetate. However data from the structurally related respective stereoisomer (nerylacetate; CAS 141 -12 -8) are taken into account for assessment.
In the chosen key study for eye irritation according to OECD TG 405 and GLP, 0.1 ml of undiluted neryl acetate was instilled into the eyes of four SPF albino rabbits (Symrise, 2000). The resulting mean scores for corneal opacity, iritis, conjunctival redness and chemosis (24 - 72 h readings over all animals investigated) were 0, 0, 0.4 and 0.3, respectively. The findings were fully reversible within 72 hours.
Overall, based on the findings for the stereoisomer neryl acetate, geranyl acetate was found to be not irritating to eyes.
Justification for classification or non-classification
The present data on skin irritation fulfill the criteria laid down in 67/548/EEC and regulation (EU) 1272/2008, and a classification "irritating to skin" (R38) and "skin irritant" (category 2) is warranted.
The present data on eye irritation do not fulfill the criteria laid down in 67/548/EEC and regulation (EU) 1272/2008, and therefore, a non-classification is warranted.
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