Registration Dossier
Registration Dossier
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EC number: 611-930-7 | CAS number: 60045-26-3
- 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
Link to relevant study record(s)
Description of key information
No specific study has been performed on the absorption/distribution/metabolism/excretion (ADME) of 3-PPB. However, data are currently available from in vivo toxicology studies performed with this substance and analogue substances. Studies on the ADME of analogue substances, benzyl benzoate, benzyl alcohol, phenylethyl alcohol, benzoic acid are also used to support the registration of 3-PPB.
Key value for chemical safety assessment
- Bioaccumulation potential:
- no bioaccumulation potential
- Absorption rate - oral (%):
- 100
- Absorption rate - dermal (%):
- 100
- Absorption rate - inhalation (%):
- 100
Additional information
All evidences presented in the report attached below ( TK Assessment_3-PPB_20150128_Final) support a rapid absorption, biotransformation, and excretion of these substances in the urine. 3-phenylpropyl benzoate is expected to rapidly hydrolyse into 3-phenylpropanol and benzoic acid in animal tissues and predominantly in the liver. 3-Phenylpropanol may subsequently be oxidised to 3-phenylpropanoic acid (PPA) by the liver ADH and ALD. PPA is then expected to be oxidised via the hepatic beta-oxidation pathway in hepatic mitochondria leading to the formation of benzoyl CoA. Benzoyl CoA then formed from these reactions may be conjugated with glycine and excreted as hippuric acid or may be hydrolysed to yield free benzoic acid which can also then be excreted. Similarly, benzoic acid is metabolised in the liver by conjugation with glycine, resulting in the formation of hippuric acid. Distribution of the parent compound or metabolites is expected to be wide into most major organs but to be transient as evidenced by extent of its metabolism and excretion. It is concluded that, like benzyl benzoate, 3-PPB may be expected to be absorbed and metabolised to more polar substances which do not bioaccumulate but are rapidly excreted mainly via urine .
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