Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
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
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 270-128-1 | CAS number: 68411-46-1
- 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
If released into water, the UVCB substance can be expected to be poorly biodegradable based on experimental data (OECD 301B). The diphenylamine (DPA) core of the substance is not readily biodegradable. Multiple branched alkyl chains are known to degrade slowly. It is considered that for most isomers (in the focus are those carrying an alkyl chain on both rings of DPA) a fast biodegradation of the DPA core is hindered or impeded for sterical reasons and that biodegradation along the branched alkyl chains is slow. Overall, although biodegradation is expected to occur in the water-soluble fraction, the biodegradation rate is expected to be too small to go below the persistency criteria.
Comparable degradation rates are expected for biodegradation in surface water, sediment and soil.
An OECD 309 on the relevant constituent of the registered UVCB substance is avaialble. Half lifes of the parent could not be determined due to an insufficient measurement of the mass balance.
Metabolite Identification and Transformation Pathway
Metabolites could be detected in the samples of the test group FT H and FS. A literature review indicated that diphenylamine can be degraded by microorganisms under formation of Aniline and Catechol (1,2-Dihydroxybenzene) [Shin and Spain 2009, Papadopoulou et al. 2018]. This information was adapted to this test item and 4-tert-Butylaniline (CAS-No. 769-92-6) and 4-tertButylcatechol (CAS-No. 98-29-3) were hypothesized as possible metabolites according to Figure 5. These metabolites were also postulated by the software CATALOGIC 301C (v.11.15, LMC Oasis). Samples from the extracts of the storage vessels for the water phase of the groups FTH and FS were selected for the metabolite analysis.
4-tert-Butylaniline could be detected as metabolite in the storage vessel extract of the water samples from day 59. This is in accordance with the radiometric analysis which showed an increase in % of M2 between day 49 and day 59.
Metabolites:
3 metabolites have been detected:
Metabolite 1: 4-tert-Butylaniline (CAS-No. 769-92-6); confirmed by analysis
Metabolite 2: 4-tertButylcatechol (CAS-No. 98-29-3) ; suggested metabolite which was finally not confirmed by analysis
Metabolite 3: metabolite, which could not be characterized
impurity Diphenylamine:
An available REACH dossier indictes that Diphenylamine(CAS: 122-39-4) is inherently degradable not fulfilling specific criteria.
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.