Registration Dossier
Registration Dossier
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The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
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EC number: 248-654-8 | CAS number: 27776-01-8
- 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
Benzyltoluene is not expected to undergo hydrolysis, based on its structural properties.
One ready biodegradability tests carried out according to OECD guidelines have been carried out. Based on these results, it can be concluded that benzyltoluene is not readily biodegradable.
Log Koc has been estimated by HPLC to be (2 isomers): 3.6 and 3.7. The mean is used as key parameter.
The registered substance contains concentration > 0.1 % of a PBT/ vPvB compound. According to the Echa Guidance R11related to the PBT/vPvB assessment, in that case, the registered substance has to be considered also as a PBT/vPvB substance.
To answer the CCH-D-2114527842-47-01/F about the persistency datagap in the Benzyltoluene dossier, the studies performed on the relevant impurity (Dibenzyltoluene: CAS 53585-53-8) were added in section 5.2.2. Moreover, the section 5.3.1 has been completed with the available data on bioaccumulation for this relevant impurity (Dibenzyltoluene).
Additional information
Biotic degradation on relevant impurity:
An aerobic mineralization study (OECD 309) was conducted with [14C]DBT Test Substances using aerobic natural water with amended solids. The tests were performed at 12°C. Two relevant compounds of DBT substance were radiolabelled : o,m-DBT, o,o-DTPM and one relevant impurity.
The half-life of DBT during the study was determined as 56.9 days for o,m-DBT, >10,000 days for o,o-DTPM, and 32.8 days for the relevant impurity (SFO model).
Degradation products were observed throughout the study in two out of the three labels. Unknown metabolites were detected in o,m-DBT and the relevant impurity and was tentatively analyzed by LC-MS/MS.
Based on this study, o,m-DBT can be considered as persistent and o,o-DTPM can be considered as persistent /very persistent.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.