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Diss Factsheets
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EC number: 915-589-8 | CAS number: -
- 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 detailed measurements on ADME are available for alkylation and transalkylation products of biphenyl with propene. Acute and repeated-dose studies with the registration substance suggests substantial intestinal, but low dermal uptake, and intense hepatic metabolism, once the substance has been absorbed.
Key value for chemical safety assessment
Additional information
Basic toxicokinetics
For alkylation and transalkylation products of biphenyl with propene, no data about ADME have been located. The acute oral toxicity study (Biodynamics 1986) and in particular the oral 28 -day study (Harlan 2014) with alkylation and transalkylation products of biphenyl with propene, provides evidence of ready systemic availability via the oral route.
Dermal absorption
No data is available. Dermal uptake is assumed to be limited as compared with oral ingestion, based on the marked differences in either profiles of acute intoxication.
For biphenyl [CAS no. 92 -52 -4], the parent compound of alkylation and transalkylation products of biphenyl with propene, dermal absorption was determined in an in-vitro skin absorption study according to OECD TG 428 (Skin Absorption: In Vitro Method). In this study with human skin samples, about 3 % absorption was observed within 48 hours, corresponding to about 1 % after 8 hours of exposure (ECHA web site - Information on chemicals. - Registered substances, URL of study:http://apps.echa.europa.eu/registered/data/dossiers/).
Additional evidence of the limitation of percutaneous absorption arises from characteristics of polyaromatic hydrocarbons: It was estimated from results of experimental in-vivo and in-vitro studies that less than 5 % was absorbable through human skin in vivo during 8 hours from a mixture containing among others naphthalene, methylnaphthalene as well as three- and four-ring aromatics (Creosote Council III Inc./USA, not published).
These data allow to conclude that percutaneous absorption of alkylation and transalkylation products of biphenyl with propene will be of the same order.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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